FIELD DETECTION DAMAGE ASSESSMENT MANUAL OIL AND HAZARDOUS MATERIAL SPILLS ENVIRONMENTAL PROTECTION AGENCY DIVISION OF OIL AND HAZARDOUS MATERIALS ------- FIELD DETECTION AND DAMAGE ASSESSMENT MANUAL FOR OIL AND HAZARDOUS MATERIAL SPILLS ENVIRONMENTAL PROTECTION AGENCY DIVISION OF OIL AND HAZARDOUS MATERIALS KENNETH E. BIGLANE, DIRECTOR ------- FIELD DETECTION AND DAMAGE ASSESSMENT MANUAL Contract No. 68-01-0113 Submitted to: Environmental Protection / Contracts Management Divit Washington, O, C. 2024; June 1972 ------- tOREWORD The Field Detection and oamaqe Aaseasaent Manual was prepared by the Division of Oil and Kazardous Materials, Environmental Protection Agency, after nmths of planning and writing With the exception of fish kills, the subject of damage assessment has not previo zsly received s jttematic treatn*nt. >ir objective was to prepare a guide for the preparation of dasage assessment r eports which will be complete in all respects and will fully east scientific and legal requirements. The Dictionary of lazardous Substances lists 329 materials anti describes pertinent data under the headings of general properUes , toxicity and detection. The initial phase of the Manual was developed using funds provided by the Office of Research and Develcpeent (152041 1. This is the first of a series of erergency response ‘sanuata. I also envis ion an opera- tion manuai to retrieve computerized emergency technical information by means of an on—scene 1 portable terninai , safety nanuals , and emergancy sçiU response handbook as a reference for instant legal and technical seals tance. Sincere gratStude is expressed to Dr. Allen L. Jennings for thia thorough review and rewriting of the sect ions dealing with the biological aspects of sampling and damage assessment. I also express appreciation to Hans 3. Crump- Wiesner for his review and editing and to Bonni.e C. Bethel (or typing the najc.r portions of the camera- ready copy. As additional data and coflnte are received, appropriate corrections and additions wilt be made to this publication. Please address your written co nta to Dr. C. Hugh Thompson, Chief, Kasardous Materials Eranch, Of fice of water Frogran Operations. tnvironnetttat Protection hg.ncy, Washington. I ). C. 20460. Dr. C Itugh Thompaon Chief Hazardous Materials Branch ‘ Iii ------- M$tARY The Manual is a field handbook for officials who are responsible for damage assessment after a spill of oil or hazardous polluting substances. It gives procedures and checklists for on-site use, with a dictionary of data about hazardous substances. Its objective Is the production of damage assessment reports which are cotlete in all respects and fully meet legal and scientific requirements. The dictionary can also be used by officials responsible for counter- measures 1 health and safety, clean-up, and restoration. In addition, the Manual provides guidelines for Federal and State officials Involved iy drawing up plans for damage assessment, instructions 1 standard procedures, and reporting forms. The Manual is to be used before a field Investigation, as a re- minder of what will have to be done; during the investigation, as a guide to techniques and step-by-step procedures; and when reporting, as a check- list on caleteness. The Introduction describes hai to use the Manual. Flow charts dis— play steps In planning and investigation, and in identification of an unknown spill. The chapters that follow begin with the initial site survey and planning of the Investigation. The Manual refers to standard methods for detection and identification of a spill and for measur nt of damage and gives rates for selection of sa ling stations and schedules. A systematic method Is reccaended for applying the field data to quantitative damage assessment. To guide the investigation and reporting, sections of the Manual deal with statistical requirements, layman’s rules for meeting legal requirements, and a check- list of details that should be in a full damage assessment report. The Appendix is divided into three parts. Appendix A is a Dictionary of Hazardous Substances. The data are those useful In the field, such as general properties, toxicity in broad categories , and si le detection and ident ificati on tests. Appendix B is a cross index of well over a thousand synonyms and trade n s. Appendix C is for use if the spilled substance has not been identified. It lists each hazardous substance against properties which should be readily observable on the initial survey 1 such as smell and color, so that the possi- bilities can be reduced to a small ni er. ------- INT OUCTLON ! ! !PP c of Manual This manual is primarily for use by Federal and State officials with on-site responsibility for field investigation of damage after a spill. It is directed to all manbers of the damage assessment team, and especially to the team leader. The manual recosiends procedures for applying established tech- niques to the specific task of damage assessment. These techniques are dealt with in detail in other publications. The user of the manual should be familiar with, and have the following available: Methods for Chanical Analysis of Water and ililtes : FA ’l971. Siolocical Field anØJ $ratory Methods for Measur1 g the Quality of Surface bitten and EffluentsEVFA , 1973. Standard Methods for the Examination of WifeiiWciVüiè aiW: 13th edifi oic AVRA , 1971. A Practical Guide to Water Quality Studies ifliãihiiT F. W.TlffriTl; n&PtA . 1969. The Practice of Water Pollution Biolpqy : fl ie5Tt i i j inflWCAfl969. investigating Fish Mortalities: K. W. ckenthuWFMtE fl7o. Damage assessmei t, with the notable exception of fish kills, has not previously been treated as a systematic subject. Federal and other standard reference works, such as those quoted here, Drovide for the training and guidance of field investigators of water pollution, but there Is nothing about sudden unpredictable spills, except In detailed reports of Individual incidents. 1 — I ------- Scope of Manua ] The aenual consists of seven chapters which deal with methods and procedures, and an appendix which is a cor endi4s of data on hazardous materials. • Chapter I: SURVEY. Step-by-step instructions on what to do, from tine of arrival until a full dage assessment plan Is in operation. • Chwter 2: CHEMICAL AM) PHYSICAL EQUIPMENT AND TECHNIQUES FOR DETECTION AND IDENTIFICATION. *iat to use in locating a spiil and making prest tive identification. The eMhasis is on portability and si l1city. for qualitative and semi- quantitative analysts. Posftive identification and quantitative analyses are not made in the field. • Chapter 3: SAPCLING. General principles on what and where to satle, for use during planning and through- out the investigation. • Chapter 4; BIOIOSICAL DA$AGt ASSES94ENT; EQUIPMENT AM) TECHNIQUES. Similar to Chapter 2, but dealing with methods for biological investigation. • Chapter 5: OMAGE ASSES9(CNT PROCEWRtS. A systematic approach to the application of field investigations to damage assessient. • Chapter 6: STATISTICS. Cant and guidelines on the use of statistics In the fteld, and the requirements for a damage assessment report. Chapter 7: REP(*T ING AM) LEGAL REQUIREMENTS. A checklist of rules for meeting legal requirements, and of details to be included In a damage report. I- ? ------- - APPENDIX A; DICTIONARY OF HAZARDOUS PDLLUTING SUBSTANCES. Each page deals with a designated substance or closely related group of substances, in alphabetical order. Data are: chemical for- mula; synonyms; description; toxicity; pre- cautions; and detection methods. The data are those useful in the field: for example, the description emphasizes readily observed proper- ties and toxicity is in qualitative terns. - APPENDIX B: CROSS INDEX. This is for use when the spill is known by name or by a group title. The in- dex shows whether there is an entry under that name or whether reference should be made to another entry. APPENDIX C: CATEGORIZATIOtl ( IF HAZARDOUS POLLUTING SUSSTANCES , This Is for use when the sDIll is not known by name. The substances in the Dictionary, Appendix A, are categorized here by readily observed properties, such as smell and color. The in- vestigator matches his observations with these categories, and finds which substances fit the observations best. The spill may be one of these. 1—3 ------- a to LIs _ the Manual The manual has been organized to correlate as closely as possible with the sequence of work, fr a n the first quick appraisal of the situation, through the development of a plan of action and conduct of the investiga- tion, to writing of the deage report. Each section is suitable for scanning before taking action, and as a checklist when planning, investi- gating , and reporting. Planning Must be developed in stages. The sequence is: • Quick appraisal of the situation, to find what Must be done at once or very soon. • Preliminary plan of urgent action. • Further, re detailed survey, to decide on the full scope of Investi gati o n. • Final plan of full investigation. The planning phase is detailed in Chapter 1 and shown in Flow Chart 1 , If the spilled substance is known by name, use the Dictionary, Appendix A . for data about it. M en the nature of the spilled sttstance is not known, identifi- cation is urgently needed, to guide your plans and actions. Use the Dictionary, Appendix A, and Categorization. Appendix C, as Indicated in flow Chart I II. The investigation Is then conducted as for a known spill. Use the guidelines in Chapters 2, 3 and 4 for selection of methods and sa linq schedules while developing the plan. Refer to Chapter 7, Reporting and Legal Requirements, before finalizing the plan, to ensure that the Investigation covers .1) possible requirements Investigation This Is shown In Flow Chart II, and guidelines are given in Chapter 5, Dqe Assessment Procedures. Make further reference to Chapters 2, 3 and 4 for methods and sa ,ling, and to Chapter 7 for legal requirements. Refer also to Chapter 6, Statistics, as soon as data begin to accrulate; use the reco nded procedures to optimize sa llng schedules, and make frequent preliminary evaluations of results. Reporting Make final judg nt on causes of d age. and assess damage in as quantitative terma as possible (Chapter 5). Prepare the report, referring again to Chapter 7. 1—4 ------- PRELIMINARY PLAN IN OPERATION PRELIMINARY PLAN REVISED FINAL PLAN IN OPERATION See Flow Chart I i Reference Chapter or section of M u&1 MtRI%ThL 8 PRELIMINARY PLAN Further Survey Water: look Bjota: look; Waterlii and test note behavior fouling FLOW CHART I: PLANNING 1—5 ------- Frcifn ‘RevEss plan’ . ri Chart I PLOW CELAPT I I ; INVESTtATIQN AND ThEP )RT S Referer e to Chapter or sectioi-i of Manual 0 1—6 ------- [ ö arrival, spiflis unknownj Seek eye-witness of spill Using the categorization by readily observablel properties in Appendix C, list the substances that have all - or most - of the properties observed. !Th __i Check each it. Appendix A: which de scriptions match best? is visible damage consistent with any? Use the recommended field detection tests to narrow range of possibilities . I possibilities eliminated 1 Apply nore rigorous tests samples to permanent labs on by site. fastest s a 1 means. J i i SELECTION THROUGH CATEGORI ZATION LIST OF P05 BIBLES ELIMINATION OF SOME FURTHER ELIMINATION SP ILL IDENTI F tED FLOW CHART III ; IDENTIFICATION OF UNfl4OWN SPILL survey] sitej I - Note observable properties of spill: smell , color, scum... . UNKNOWN SUBSTANCE SPILLED READILY OBSERVABLE PROPERTIES Some F Spill identifie j 1—7 ------- CHA TER I SURVEY 1.1 introduction The most urgent action on arriwai at a site is to find whether there are any samples and observations that must be taken at once to avoid loss of valuable evidence. make a quick survey of what has to oe done, so tnat tne necessary resources Cai be assembled. The following actions cover the period from arrival to startinr 1 work on a damage assessment plan: + Contact the On-Scene Coordinator (DSC). • View the site. • Assume that tne damage assessment will be used in legal proceedings. (Review Chapter 7) • Make a sunrary of available infonsatirn about the spill; what was spilled, when, where, and how much. If the nature of the spilled material is not known, fi est yate it once. Use the categorization of hazardous pollutinc suostances in Appendix C as a guide. Make sure there has been a spill. • ake a sucnary of known and suspected damage. Detennine if there is a threat of future damage: e.g., downstream. • Decide what samples and observations must be taken as soon as possible. • Begin this urgent sameling. • Decide what samples and observations must be taken in the near future. • Prepare for this sampling. - Make a preliminary plan for fufl damage assessment. Things to consider are: Water uses damayed or tnreateneO: r unicipal, industrial, agricultural; fish, wildlife; vessels, structures, fore— shore; recreational uses and habitabflity for man. 1—1 ------- Samples to take: water; fish, shrimp, etc.; benthos; periphyton; plankton; plants; snoreline and inshore. Records and witnesses needed: soul and its moyenent; damage and other effects; weather. Discuss preliminary damage assessment plan with OSC. Find whether countermeasures will affect damage assess nt, or damage assessment interferes with countermeasures. N lsCuSs soecial hazards: toxicity, flamabilitv, explo- sion ootential, etc. (Consult the Dictionary, Appendix A.) Modify the preliminary plan accordingly. Set the plan in operation. Cafl for men and equipment as required. Alert central laboratories to wbi- h you expect to send samples. Report status, accoroing U’. standing Instructions. 1.2 First Observations The first observations macic at the site influence the whole Investigation. They can also be the most Important part of the recorded evidence. Observe as much as you can personally. Draw on local knowledge; a game warden r fisherman may best be able to see changes in a familiar environment. However, use this local help critically and under qualified supervision. The following actions are usually the most important to take after the first quick survey. Think, however, about further special needs for each case. Consult the OSC and local a.zthorities for sources of local knowledge. Survey the site. This is an extension of the quick viowing on arrival. Note the appearance of the water. 1—2 ------- • Observe fish behavior: gasping, crowding, moribund, dead, absent. • Observe behavior and appearance of other vertebrates and of invertebrates. • Observe appearance of plants: fouled, patches f damage, dead. Severely damaged vegetation may n t be s b1 dead for some time. • Record fouling of banks and structures. Be continually alert for abnorma l odor. Look inshore for abnormal appearance of animals and plants. - Record the weather at the time of spill and survey: air and water temperature; precipitation; wind; sunshine. 1.3 Weather Observations A record Is needed from before the soill to the end of the investigation. The important factors are: Air temperature; not less than 4 readings oer 24 hours, oreferably more. Water temperature: not less than 4 readings per 24 hours, including early afternoon; oreferably more. Take surface temperature, and subsurface temperature at one depth or more. • Precipitation: descriotion , daily total, and note of abnormal intensity. • Wind: speed and direction, not less than 4 readings per 24 hours; more if moveqient of surface pollutant is important. Sunshine: daily, in general terms (sunny, sunny intervals, etc.) In tidal waters, schedule observations by tidal cycle and not the clock. Take readings at high and low tide (most imoortant) and mid-flood and mid-ebb (less important). This applies particularly to water tempera- ture and wind. 1-3 ------- Take the following actions to get these records: • Set up observations at the site if possible. • Look for nearby official weather station: .ationai Weather Service, military installation, Ccast Guard, air pal Ration authority 1 etc. Ask for an expert tx ir c’n or the applicability of their recDrcs to the SP ii site. • if there j5 ftjiy operational weather station nearby, seek a Coc.per:itive Observer (nar e from National Weather Service), forest fire watcher, etc. • In unsettled weather, always seek on-the-snot evidence. Locally heavy rain or high wind often miss all reg lar observing stations. 1.4 Planning iolpjfca2 Sarnp j j Pay special attention to requ reinents for biological sampling, which is the major problen in damage assessment. Every site and incident is different. Make decisions on: • Live conrunities to sample: benthos, plankton, fish, etc. • Moribund or dead sarerles to take: fisn, crustacea, etc. Types of habitat to sample: riffle, pool, mud, various depths, etc. Since each r,as a different bicta, sample all major types as a general rule. Size and disposition of sampling stations, and rntlbers of grab samples , These will probably have to be revised when some sampling results are available. As a generai rule, take at least three samr’les eac! time at each station. • Control samples: wt at aM where. • Water aM sediment sa ’pies to oe taken. Sequence for nini jisturbance o later s xnples: e.g., take water and plankton sanples t:fore disturbing the environment by use a -f dredges or grabs. Urgent sampling, such as dead fisn which nay be lest through water movemnnt, 1-4 ------- Give full weight to the wide seasonal variation in stssceptability to damage of various parts of the ecosystem. This variation includes three componeats. Environment — Variation in quality of envrionment alters the importance of added pollution. Exatles: a spill of high—BOO material is more serious if DO Is seasonally (or diurnally) low; zinc Is more toxic In the presence of copper. Increased temperature Increases susceptibility of fish to degraded water quality; low DO similarly Increases susceptibility. • Cotnnun lty - Life cycles of residents and movener ts of migratory species modify the composition of the comunity at risk. Examples: ininature organisms may be more sensitive than - adults; specific populations may be present or absent depending on the season. Individual organisms - Some species are more susceptable than others. 1.-S ------- CHAPTER 2 CHEMICAL MID PHYSICAL EQUIPttNT MO TECHNIQUES FOR DETECTION AND IDENTIFICATION 2.1 Introduction This chapter deals with methods for use on site, in support of a damage investigation. There are two apolicatlons: Detection , for locating a spill and tracking its spread. Identification , for what dnage to expect and interpretation of observed damage. These require only qualitative and semi—quantitative tests. A fully equipped permanent laboratory must make all oositlve Identifica- tions and quantitative analyses quoted In the damage renort. The methods are convenient for use at the spill zone or in mobile or Improvised facilities nearby. They are mainly for water samnling and also include samol lng of ground 1 vegetation, etc. for spilled material. Detailed orocedures are not given. For these, the user must refer to standard works such as Methods for Chemical Anaj js of iater and Wastes: EPA, 1971, and Standard Methods for the Examination of Water and Waste - water: APHA, l97T whfch should always be on hand. 2.2 Sampling Procedures Consider conditions before selecting procedures: what is to be tested for, how soon, by w%at method, etc. Refer to the standard texts above and to 45Th Snec. Tech. Publ. No. 148-1 and USGS Water Supply Paper No. 1454. Select samplers to suit proposed analysis: e.g., avoid metallic construction for metal analyses, avoid unapproved plastic for PCB analyses. Rinse samplers and sample bottles with the water to be testecL Refer to Chapter 3 for guidance on sampling locations and schedul es. Sample surface filr by partly submerged wide mouth bottle or the ‘ dustpan technique”. 2- 1 ------- • Take sediment satples even if there is no irrediate evidence of bottwi contamination. • Look for spill meterial at waterline and inshore. Scrace structures, take vegetation samples, mud sanDles , etc. 2.3 Sample Preparation - Clear turtid samoles by filter or centrifuge before tests for precinitation or color change. • Do not, however, orit to test the renoved solids, on which the spill may be bound physically or c!!eceically. • Treat susoended organic matter by ado oxidation i’ ’ low concentrattons of metals are souaht- 2.4 S&npje Preser,at ion • Always test srrles as soon as oossible. Some tests must be done at once temr’erature. pH ; others may be delayed. • Use oreservative measures whenever aot’ropriate. • Record preservative !neaSurr , and elapsed time from s utnling to test. • Test preservative before use, if It could unset resu!ts e.g., test acids for trace metals. • Dark and cool storage Is usually beneficial. • Acidify samples for metal analysis at once with nitric or hydrochloric acid, S r I ner liter. • Int’nt it nicroflora in biodeoradE- le sa rles: refriperate, and use an sprro rtate nreservat lye. Ensure t iat sanole containers an closures will not alter the samole by addin trace retal, absorbing pollutant, etc. 2.S Selection of Test Me T hod • Simplicity, convenience and speed of results are usually jch more iwrertant than refinement of technique. Use a c nercial detector or kit whenever possible - Examp les include test paper or oortable meter for p4, portable Dfl meter, end kits for specific metallic ions and families of organic compounds. 2-2 ------- • Vapor detectors may be unsuccessfUl because of low vapor concentration and Interference by water vapor and other volatile matter. • Do not expect manufacturer’s claimed sensitivities in the field. They apply to samoles of “purer material or water, not to samples of mixtures in a polluted environment. • Wet-ch iical tests are recownded for many substances in Appendix A. They are generally more prone to background interference than the kits. Cross-check identifications made by kit or wet-ch jical test whenever possible. Use more complex instrtsnents if necessary, in a mobile or improvised facility. Three are of wide usefulness: gas chromatograph (GC), visible— I S V spectroscope (uV), atomic absorption spectroscope (AA), and Infrared spectroscope (IR). Select GC coltnn (support and liquid phase) with due considera- tion to substance looked for and to presence of water. Select CC detector for the intended purpose. Thermal con- ductivity Is widely aoplicable but less sensitive (lo to io- gramsj. (fydrogen flame and electron canture are more sensitive ( lCr° to lo- gram) and fairly specific to hydro- carbons and oolar compounds respectively. A heated colni is desirable. Check CC identification with a similar reference sample if possible. ISV absorption spectra give some separation or simple alt- phatics (200 to 250 m lllimicrons) from higher arcinatics (300 to 400 in lllimicrons), and may give specific identification (e.g., acridine). PA is good for most metallic ions, at sensitivities of lO to 10-b grams or better. Be alert for background interference at these high sensttivities. 2-3 ------- • IR is the most versatile for identification of organic materials. Sample extraction may be required to reduce interference by Water. 2.6 Checklist of Equij ent The following is a checklist of equinnent that is generally useful in the field. It should be modified by local circumstances and individual preference. Use it as a guide to what should be drawn from a wider range at the base stockroom to investigate an unknown spill: a known spill requires less. Use it as a basic list for equipping a stand-by vehicle. eneral equ ent Water sampler, sediment sa v1er, scraoer, trowel. Sample containers 1 labels. Ice chest, chemical preservatives. Reference texts: Appendix A, references in 2.1 above, etc. Glassware. Butane burner or similar. Filtering apparatus and papers, and/or hand centrifuge. Thermometers and portable temperature probe. p H test papers and portable meter. Portable 90 meter. Distills water. Kits About half of the designated hazardous polluting substances can be adequately detected by one or more of the full range of camnercial kits, such as those supplied by Hach, Kitagawa, ‘5A, and Scott-bavls. Keep a ci rehensive stock at home base. Draw appropriate kit for a known spill. Draw a few widely non-specific kits for an unknown spill: the choice depends on stocks and other circirstances. Renents The following list coven more than 801 of the detection and identification tests given in Appendix A. 2- 4 ------- Acetic Acid M&gnesi w lt Acetone Malonic a cid Alizarin Mercnric Acetate Ammonia Methanol Ajiurtonium molybdAte Methyl iodide Anmonium sulfide Methylene blue Annonium thiocyanate NeSSIerTS solution Aniline Nickel chloride Benzenesulf onyX chloride Nitric acid Benz idine acetate p—Nitrobenzaldehyde Bromine in carbon tetrachloride p—Nitrobenzoyl chloride Carbon disulfide l—Nitroso-2—naphthol Ceric annonium nitrate Oxalic acid Chromotropic acid Periodic acid Copper acetate Phosphoric acid 2—2’ Dipyridyl Potassium chromate EDTA Potassium cyanide Ethanol Potassium hydroxide Ether Potassium ferricyanide Ferric chloride Potassium ferrocyanide Ferrous sulfate Potassium permanganate Fluorescein in alcohol Rubeanic acid Hydrochloric acid Silver nitrate Hydrogen peroxide Sodium carbonate Hydrogen sulfide (sat.soln.) Sodium hydroxide Hydroxylasnine hydrochloride Sodium iodide Iodine Sodium sulfate Lanthanum nitrate Sodium sulfite Lead dioxide Sulfuric acid Lead nitrate o-Toluidene 2-5 ------- NOTE; Some reagents are conveniently carried in more than one form: e.g., concentrated and dilute mineral acids, aqueous and alcoholic potassla hydroxide. bIle or improvised laboratory If a mobile laboratory is to be equipped, or a room with basic utilities Is available, some useful itens of equipment become practical wtiich would otherwise be marginal or impractical: Bench centrifuge, electric powered. Distillation appartus. Ion exchange coins with resins. Thin layer chromatography apparatus Potentlometric titrator. Light—scattering photometer for detecti nq preci p1 tate ’s. Balance (coarse). Gas chrtsatograph (at least 10-15 coltrns and 2 types of detectors). Ylslble-UV spectrophotometer. Atomic absorption spectrometer. Infrared spectrometer. 2-6 ------- CHAPTER 3 5& fLI HG 3.1 Introduction Sampling for damage assessment includes the water, organisms, and sediment in the spill zone, and control samples taken outside the spill zone. Test water quality in situ (e.g., by pH probe), or take samples and usilfeld detection kit, to find the extent and movenent of the spill. • Look at organisms in situ, or take samoles for local examination, to determine the nature and extent of damage. Send samples to a permanent laboratory for further examination if necessary. • Take samples of sedl.ent, for comparison between sai ling stations (see EPA Biological Methods Manual). Take samples of water (and sediment where appropriate) with all biological samoles. All samples for positive identification of pollutant, quantitative chemical analysis, or pathological di- agnosis must be sent to a permanent laboratory. Plan to sample organisms In these five groups: • Were exposed to spill - found at site of spill or in path of contaminated water. Now exposed to spill - found in present zone of contami nation. • May become exposed — found in predicted zone of contamination. • Harmed or dead - found anywhere that has been at risk. If biological damaqe is seen outside the risk area, take samples for comparison with samples from the spill zone. Control samples - from any location not exposed to spill, but otherwise similar to the exposed locations for which they will provide controls. 3- I ------- The ability of organisms to move or be carried by water currents affects their value as evidence, but is not the only consideration: Although freely motile organisms (fish, birth) qive the least definite evidence of spill effects or as controls, because of the doubt whether they were exposed or not, they must be examined and sampled if they show damage, especially if they are economically Itortant or legally protected. Innobile organisms (benthos, periphyton) give better evidence of spill effects because there is less doubt whether they were exposed or not. • Plankton tend to remain either in or out of the zone of contaminated water. 3.2 What Biological Samples ? • Give priority to species of economic value (conercial or sport). They may be damaged in value without being killS or even reduced In vigor, If tainted or toxic to hans . Do not forget delayed damage: future crops may be damaged by injury to eggs, Irature organisms, or breeding adults. Give special attention to benthic Invertebrates, which link producers and secondary const rs and generally retain a print’ of damage for some time, being rela- tively isobile. • Look for daage to other links In the food web: for example, plants that support aquatic and littoral life through links such as detritus—mlcroorganlsm—mollusc, or plant-snail-bird. Marsh plants are particularly Iizportant in estuaries. Take samples f periphyton and plankton for their qualitative and quantitative value, especially pert- phyton in streams and plankton in estuaries. Look for species width might be expected to be pre- sent. Their absence may be evidence of damage. Look for records of recent and long-term presence at the site. 3-2 ------- • If there Is persistent degradation of water quality after a spill (e.g.. slightly soluble material re- maining on the bottoms or a spill into a lake or reservoir), consider bioassays t , In situ or in the laboratory. Choose fish, Invertebrates, or enbryos as test organisms, according to economic importance or technical suitability. Consider also artificial substrates for natural colonization. Always conduct control tests outside the soul zone. 3.3 What Water Samples ? P’an your water sampflig, within and outside of the spill zone, to answer questions such as: What was soilled, and how much? • Where is the spilled material, and in what concentration? Where will the spill go? What water uses are threatened? What was/is/will be the exposure of the biological connuni ties sampled? What was the ore-spill water qua’ity? This may be inferred from reference samples. Was there other pollution which could have caused or augmented the damage? • Is “normal” water quality being restored, or has it been restored? Sampling must be scheduled to look for large diurnal or other fluc- .. cions in water quality: e.g., in dissolved oxygen, pollutant burden. turbidity, or temperature. These could strongly influence the effects of the spill and subsequent events. See 8Tologflcai F ie ld and laboratomy Methods , EPA, 1973; Standard Methods for the Examinatf&s iTwater and Wastewater , 13th edItion, AF} ,1971. 3-3 ------- 3.4 Where to Sa le: Diffusion and A spill in water is diffused (soread) by stirring rovenents within the water. At the ste time it may be transported bodily - e.g., by river flow. Surface material is affected by wind. Knowledge of diffusion and transport helps answer questions such as: • What area has been exposed to the spill? What area wi l l be exposed? • Where to sample water and organisms? Direct knowledge of the specific site Is the best guide, but not often available. No two bodies of water are identical, and none Is the same year round. Take the following action: In conjunction with the USC, seek data which may have been collected by the Geological Survey, Corns of En- gineers, State water authority, Storet, or The National Field Investigative Center, or nearby universities. If available data are inadequate, make estimates with the help of the guidelines in 3.5 below. • Progressively build up a picture of local water movements as detection of the spill and observations of damage add data. Consider whether experiments with dye tracer or floats will be useful (e.g.. to measure time of travel downstream). Rater that the value of such evidence depends on identity of conditions: flow, tide, weather. 3.5 Spread of Spill in Typ cal Waters River Characterized by unidirectional flow. Stratification not c on. • Vertical mixing: usually rapid; soluble spill will difuse from sw-face to bottom in a few tenths of a wile, and much sooner in shallow, turbulent flow. However, thenaal stratification may markedly suppress vertical mixing. * A leading reference is A Practical Guide to Water Quality Studies of Streams , F. 1. Kittrell, flIPCA, 1969. 3 -4 ------- * Lateral mixing: sl er than vertical mixing, and much more variable; in an DaverageN river, it may be complete within a few mIles. However, lateral mixing takes much longer In a wide, shallow, turbulent river or a wide, smooth, straight river; it is faster in a narrow, winding or stratified river. • Longitudinal mixing: the first detection of a spill down- stream may be earlier than expected on the basis of flow data; the last trace may be much later, because of hold- up in shallows, eddies, or dense vegetation. As a general rule, use measured surface speed plus 25% to calculate time of first arrival. Lake Characterized by no set flay; marked effect of wind. Thermal stratification Is comon. It is difficult to predict the spread of a spill even if data are available from earlier observations. Use evidence of visible damage, fouling, or discoloration as indicator of where the spill is or has been. Also use qualitative and quantitative biological satrçles such as benthos or plankton. Use water quality or wet chemical (Appendix A) tests to detect and track the spill. • Make full allowance for wind: floating spill moves on average at 2% to 3% of the wind speed, perhaps as much as St. Use wind measurements taken at the site if possible. If wind records from some distance away must be used, seek meteorological advice on their applicability to the site. Make allowance for thermocllne (known or detected) in limiting downard diffusion or preventing upward diffusion from below. Sançle at various depths, guided by the therniocline or other evidence. Estuary Characterized by net surface outflow, bottom inflow; retention at the salt/fresh water interface (halocline); affected by tide. Determine the present fresh water input: is it normal, more, or less? • Take note of wind, present and since spill. • Seek data which are often available for surface currents and effects of wind in major estuaries. 3—5 ------- - Iook for damage, and make qualitative biological and chemical tests to deteraine the present and previous location of the spill. Take account of the v nent of the “salt wedge”; use avail- able data or make observations. Expect the soill to recycle with the tide, unless there is strong f lushinq by heavy fresh water runoff or high wind. Coastal Characterized by tidal currents, and there may be a large net flow. l arked wind effect. Look for effects of local configuration on mixing and flow. Look for retention of spill in pools and lagoons. • Expect recycling with tide. • Loot for Intermittent expOsure to so ul of different parts of the coastline, under the changing influences of tide and wind. 3.6 Effect of Water on Spilled Material In addition to transporting and diffusing the spill, the water may change it physically or ch ically. Examples are: - Hydration of anhydride to acid. Hydrolysis of metal salt to hydroxide and acid. • Eimalsiftcation. so that insoluble material behaves in many respects as though dissolved. The soul may also be affected by substances dissolved or susoended in the water. Ex ples are: Neutralization of acid by alkali. Adsorption on susoended particles and deposition as sediment. Reduction of oxidant by organic material. 3 -6 ------- 3.7 S 1lng Fish ( 111* A fish kill requires special attention because it is the form of damage that most often arouses ptthlic concern and Is the damage to which a dollar value is most readily assigned; most States have establi shed dollar values for fish killed. Use fish kill procedure as a model for other investigations: it is the most highly developed form of damage assessment. Counting • Count all (or most) of the fish kill if possible: i.e., if smell m ister, or within small area. • If the fish kill is too large to count all fish, select representative sampling stations, report h ut they were selected, and sithstantlate the selection with evidence such as photography. • Count fish In situ or collected by net, etc. Take account of movement of dead fish by current or tide. In tidal waters it Is advantageous to have several crews counting at once. • Look for evidence of loss to scavenging animals. • Calculate total kill from sample counts and multiplication factor (total are a/sampl e area). Don’t overtount. At Intervals, make a quick estimate of the total kill. Stop counting when It is evident that fur- ther counting will not significantly alter the estimate. Taking Specimens - Collect specimens of all species of affected fish. Collect similar m ers of control (unexposed) fish. (See instructions below on nfler of fish to collect). 4s a rule, take affected fish at more than one station, and especially If the area is large or there is evidence of locally different conditions. Preferably, take control fish at more than one station, and especially if the first control samples fail to match alt samples of affected fish. * See Investlg4tinqjjsh Mortalities , kit. Mackenthun, FWPCA, 1970; Biologicatfield and LaboratorsiPwthods, EPA. 3-7 ------- • If the fish ki?? continues for more than one day, take further samples. Take further samples of affected fish if the first specimens were of doubtful value through being dead for an uncertain period. • Check your sampling plan by reviewing use that will be made of the evidence. • Look for factors other than the spill that might have caused or augmented the kill: e.g.. “red tide”, severe weather. • Consider whether there might be different successive causes of fish kill, or different causes in different parts of the area. If the spill is seen to affect fish in a new area (or Is expected to), give top priority to watching and recording behaviors and to taking soecinens of fish and water before and durino the event. Observation and sampling of an on- going fish 1111 gives the most favorable opnortunity for successful diagnosis. Number of Diagnostic Specimens Preferably, sample all species affected; at the very least, sample representative species of imnortance either economic- ally (e.g., sport fish) or ecologically (e.g., herbivore, niscivore). Take the following se ples of each s ’ecies at each station: • For laboratory observation of gross signs, and chenical analysis of selected tissues (preserved by freezing) - 10 fish, or not less than 10 lb. (if practical). For histooathology (preserved in 10% formalin) - S small fish. - For infectious disease diagnosis (nreserved on ice) - 5 specimens of dyine fisn. For irnediate exarinatipn on site, samnie until a consistent picture has develooed. Packir.g and Shippj g S ecFnens Alert the receiving laboratory as soon as possible. 3-8 ------- • For laboratory examination and chemical analysis: Pack in individual plastic bag 0 seal and label. Quick freeze In freezer or with dry ice; shin with dry Ice. Controls should be frozen at the same time. • For histology: Pack with tenfold excess of 10% formalin or fix in excess and ship with small amount of fresh fixative. Fixative must have access to organs. For smaller fish (less than 6 in.), make abdominal incision, clip opercultn, cut above and behind eyes Into brain cavity; for larger fish, remove and fix organs separately, or at least remove membranes. For infectious disease diagnosis: Pack In Individual plastic bag, seal and label. Ship in insulated container, preferably leakproof, with ice. Deliver to diagnostic laboratory withIn 24 hours, preferably much sooner. Plastic bags are best enclosed in a second bag. Allow for expansion if air freighted. Glass jars (with glass closure; home cannIng type) are acceptable. Surround with adequate padding, and absorbent for small leakage. In emergency, replicate histological saiiples ( jx ) may be packed in one container. Wrap each specimen In a piece of paper towel of good wet streagth. For taste-testing (if there is a question of damage through tainted flavor): Fish should be dressed and frozen quickly; ship with dry ice, and protect carefully from becoming tainted In transit. Freeze blood samples and ship in dry Ice. Label to correspond with fish fnn which taken. Send with the samples any details which may help diagnosis, such as observed signs and suspected cause. Do this even If a reoort is being sent by other means. 3-9 ------- 3.5 Senthos 3.8.1 Sa ling Stations • Always sample for comparison .f like with like (e.g.. riffle with riffle), in any assessment that depends on comparison of test samples with one another or with reference saiples. • Ithen sampling for exposed organisms within the spill zone, try to avoid habitats which cannot be matched by contrvi habitats outside the zone. Prefer habitats that favor a large and dfvene cosrsainfty; e.g., shallow riffle. • Take at least three replicate samples at each station. This is n’y important for statistical purposes. The n er should be decided on the basis •f what is found when s ies are examined; see Chapter 6. As a general principle 0 eliminate a station rather than take less than three samples. In a lake or reservoir, take samples at Increasing depths on transects perpendicular to the shore. In an estuary, gtve due weight to surface and subsurface net fl 0 tidal excursion 1 and wind effects in selecting s lin stations. 3.&2 Examination The st important data are the kinds of organisms and their numters,, in each separate sample. These data are used to cakulate: Composition of each cmmmanity, in terms of a diversity Index or other asure. Population density (niSer per unit area). • Variability between sales at one station, dilch Is related to adequacy of sampling. • Variability between stations, within the spill zone and outside, which is related to damage. 3-IC ------- Initial evaluation may not require ccrplete species identification. Consider carefully thether the labor of goinq beyond broad taxa (order of family) W ill add sig- nificantly to damage assessment . The decision is not irrevocable, because specimens e r nst be kept until •the case is aver, • If results are not urgently required, send samples to a permanent laboratoQ for examination. • If preliminary results are urgently required, examination with adequate identification can be made on site, in a mobile laboratory or improvised facilities. A semi-quantitative examination by sorting Into groups of like organisms without identification may be made If qualified staff are more urgently engaged elssiere. This Is not an acceptable substitute for regular examination. Other data that may be taken are mortality and aboornal appearance. As a general rule, and especially If damage is seen or suspected, retain samples for chemical or radiological analysis. Refrigerate or freeze: do not use chemical preservatives. For other than chemical or radiological examinations nserve samples In 10% formalln. ? tr1W y n and lankton The examination of periphyton and plankton follows the sama general principles, aimad at sptcies diversity, population density and sample variability; but results may only be semi-quantitative. Measure of Uaniaq + Use bionass within a trophic level (or comnunity) and species composition as a measure of damage tp the food chain. • Use the yola occupied by preserved specimens (in standard sarple bottles, frun comparable samples) as a simple indicator of decrease in bf amass caused by a spill. It provides good material for a photograph that may be Included in a report; e.g., a series of upstream, spill zone, and downstream samples. • Take tare that preserved specinens d c net Include maiy organisms that were killed by the spill but not deccrposed or dispersed. 3-Il ------- 3.11 lonq-Term Surveillance • Decide, early in the Investigation, whether to reconrend long-ten surveillance. This decision may be provisiona l , • Long-ter, surveillance is required if damage is likely to be protracted or delayed by; wcontinuousa spill, for ezancle by slow seepage. Persistent toxic spill of material with low solubility and density 9reater than water. Lag in natural recovery. Future catch of fish damaged by harm to l,mnature or breeding fish, or to food web. Surveillance may involve: Physical and ch a mical monitoring of water quality. Observation of bthloqtcal effects In situ. Observation of recovery. Taking bfologfca) specimens for histology, chenlca l analysis. etc Exposure of artificial substrates for benthos and/or periphyton. Bioassay in situ. Cloassay hf Viflaboretory. Records of caw*rcial catches. TM duration of damage Is l’w’ortant If damage is to be assessed in terms of, e.g., man-days of Oeneficta) use denied. Consider use of bioassay In situ for circumstances such as long-term exposure of oysir s to pen Istent cont3mlna- Lion. wire use of sown oyster trays should give strong confirmatory evidence. 3 -12 ------- CHAPTER 4 BIOLOGICAL DAMAGE ASSES SMENI: EQUIPIENT AND TECHNIQUES 4.1 IntroductIon Chapter 2 deals with m thods for detecting the spill. The present chapter gives guidelines on equi xaent and techniques for observing the effects of the spill. This is only an outline of what is most useful for the specific task of damage assessment. It is not a comprehensive guide to field methods In aquatic biology, for which reference should be made to publications such as Methods for the Collection and Anal is of 8iolqj cal SaJ ples, EPA, 1973; Standard Methods for the Examinatl&nof iiiiir and Vastewater (13th Editfon), APHA . 1971; The Practice of Water PiflutTóWTioloM, K. N. Mackenthun. FWPCA, 1969; Tnvesti fling Fish MortalitTes , K. H. Mackenthun, FI1IPCA, 1970; and EPUTra n ng Manuals. Sampling must be supervised by a qualified individual, who Is responsible for selecting the best equipment and techniques for each Incident and for data evaluation. Qualification is determined primarily by credi- bility as a witness in court: training, experience, and ability to present evidence convincingly. 4.2 Selection of Methods Ask yourself whether your proposed methods are: Technically defensible, and/or generally accepted, and quoted In standard texts such as those referenced abovel • Suitable for collecting statistically sound samples? • Suitable for gathering c ,arable test and control sanoles? Able to collect adequate samples within the manpower and time available? Able to give quick preliminary results? Fully adequate for economically inportant species? • The best overall for evidence about this spill? The ones you are accustomed to, and prefer to use? 4-1 ------- High standards of perfonnance, care, and documentation are as important as standardized methods. However, consistently uniform procedure is most important when the damage report hinges on comparison of test and control or reference samples. This is especially true in the statistical evaluation of the data. Select methods to look for effects that show damage to man’s beneficial uses of the spill area, or that help the thvestiqation of damage. Prepare to report fully on: - Nature of damage: what organisms and water uses were harmed? in what way? - Extent of damage; how many fish killed? how much shoreline fouled 1 how severe was the damage? how long did it last? • Cause of damage: what was the substance that did the damage? (The question of where it came fr a n is not a part of damage assessment). 4.3 Blolo ilca l: General Decide which of the following groups of organisms are to be sampled: • Organisms always within the water (benthos, periphyton , plankton. ne kton) . These usuafly provide the most useful evidence. Sampling Is mainly by dredge, trawl, net, etc. SCUBA visual survey and sampling may be a great help. intertidal organisms. These are exposed to the spill only if the tide Is In while spilled material Is present. Thorough sa ltng of quadrant or transects t s practical, under visual control. Inshore, labile organisms. Exposure is limited to abnormal conditions of heavy vapor concentration or airborne spray. Sample only if there Is observed damage or report of high wind and storm tide. • Water surface and inshore, mobile organisms (Insects, birds, littoral manaals). These are the least likely to give useful evidence. Prepare to sample only “damaged” specimens, and r er that it may be uncertain where and when they were exposed, unharmed specimens are of little value (especially as controls): were they ever at risk? 4-2 ------- 4.4 Benthos The choice of sampler is determined by the character of the substrate and other circumstances.. Use a grab (gravity-closed or spring-closed) for sa mples including sub- strate and organisms within it. The Ponar is preferred (less liable to displace epibentriic organisms), Van Veen (for its strong ‘bite”) Ekzan, etc. Keep a sample of substrate from each station, for: Comparison between stations. Chemical analysis, to correlate with heavy metal, pesti- cides, etc., found in organisms. If conditions permit, wash samples on site through a U.S. standard 130 sieve. .1ashing is better done before pre- servative embrittles organisms, and you will have less material to transport. • Check samples washed on site for their imediately visib’e qualitative ev idence of the adequacy & sampling. Are the numbers of organisms enough for statistical purposes? Are samples from any one station abnormally variable? Use the washed samples also as a preliminary guide to extent of damage. Decide whether the sampling plan should be revised. (This point is made here, rather than in Chapter 3, to snow the value of seeing innediately what you have collected . • Use the Surber sampler in shallow riffles. Take care to be uniform in the selection of riffles, thoroughness in working substrate, and deptt worked. Keep a sample of substrate. Use trawis, where needed, to collect bottom-associated molluscs. Collect crustaceans, live and dead, with a grab sampler in winter; they are likely to be in the substrate. In sunner, use a bottom trawl. Do not use baited traps, which ‘may be too selective. Use SCUBA where possible, to check trawling operation for consistency of sanoling. 4-3 ------- 4.5 Periphyton The periphyton may supplement evidence from the benthos as to linear extent and severity of dage. Quantitative results are difficult to obtain except with artificial substrates, which are useful for damage assessment only If long-term surveillance is planned. S ,le periphyton (whenever practical) by r movlng portions of substrate, scraping, and washing off Into a container. - To sample in situ, scrape substrate and hold a fine-mesh net close mM5tre . - Uniformity of procedure is essential if samples are to be ciwared. If samples of periphyton or benthos are taken for chemical analysis, preserve by refrigeration or freezing, not with chemicals. 4.6 Plankton In general, use a water bottle sampler for phytoplankton and a net for xooplankton. • Use a non-metallic water seler (e.g., plastic Van born), especially If samples are to be analyzed for trace metals or used for primary productivity or other metabolic rate measurements. Prefer a metered net if quantitative zooplankton samples are desired - but uniform tmvs with an urretered net are acceptable. Select net mesh with the intended samples in mind. DO not use unnecessarily fine mesh, which may clog. A water , dip tube, and filter may be used for plankton, but is not recoamended for delicate algae or larger zooolankton. 4.7 Fish • Collect floating dead fish by hand net fras shore or boat. • Collect dead fish from the bottom by hand net, if In shallow water, or SCtEA if deeper; alternatively, search with any available bottom trawl. 4—4 ------- • Always attanpt bottom inspection or sampling if there is any indication or suspicion of fish kill. • Select collection aetI ds for live control fish according to the species and sizes found dead. E.g., use bottom trawl or mid-water trawl for active collection in a species’ known habitat; use gill net for highly selective collection of a particular species and size. Refer to the EPA Bioloqical Field and laboratory Methods . • Use the haul seine for general collection in shallow water, unless bottom snags interfere. Consider advantages of electrofishing (in fresh water). 4.8 Vascular plants may show visible damage (often after delay) or may act as collectors for contaminant. Recoamier4ed equipment Includes map or chart; Polaroid camera; grappling tool (rake) aw knife; SCUBA; frames, and cord and stakes; sample containers. • Before sampling, survey the area on foot , by boat, or by air. • Select plants for sampling by: Visible or expected damage. Adherent containi nation. Fcologlcal importance (as food directly, as detritus, or as habitat). • Give careful consideration to the value of aerial photography (visible or hR.), probably at several time intervals, in a large-area incident, or if quantitative sampling of macro- phyton is hard to achieve because of difficult access or irregular distribution of species and density. 4.9 Intertidal and Inshore Zone • Sample small and numerous organisms within a frame of I or less. 4-5 ------- • Separate from substrate according to its nature: e.g., wash clay sa les through a screen; hand pick and brush or scrape pieces of rubble, and wash into a container. Count and sample large and scattered organisms (e.g., dead birds) within transects of suitab’e extent. Randomize quadrant and transects with due regard to circum-. stances: e.g., if organisms are grouped In narrow zones parallel to the shoreline, they are best sampled by transects perpendicular to the shoreline. • Select methods with extra care if there is damage to animals or plants that attract unusual public attention. For macroo!iyton, see 4.8. 4.10 Other Da! Damage to man’s beneflcial uses of a body of water and its irr-ediate vic nlty may also affect: Pecreational use, habitability for man, and aesthetic values. Property - structures, vessels, beaches. Withdrawal uses - Industrial, municipal, agricultural. Your lnvestigatthn of these will be mainly by visual observation. Interrogation, inspection of records, and samplinc for extent and nature of contamination. Basic equipment is: Notebook, suitable for permanent record. Tape recorder (especially helpful when time presses) - Camera; Polaroid for preference, and color may be very useful. • Maps and Charts; one i roortant use is for narkinp as ? nart of the recora. Ch ical detection kits, sample jars. Procedures must be developed to suit each unique occasion. L se C hacters and 7 for ui ance on wrat is to be acconnljshed and wnat is to ne reportec. - 0 ------- 4.11 ChecklIst of Equi nt This is a checklist of equipment that is coinrnly needed for field assessment of biological damage. Use It when preparing for an in- vestigation. The specifically naned Iten5 are typical ones, pot Intended to exclude others that may be available or preferred. Accessory items (such as string, tape, tools, tow lines) are not covered. The list is arranged by funct ion as a Teerinder of what should be available for each field task that is anticipated. ene Notebook Tape Recorder Labels, waterproof Soft pencils (or other waterproof, non-sntidglng markers) DO meter and kit pH meter or paper Chemical test kits sample bottles, various Specimen containers (Including plastic bags) Sealing tape Preservatives (ronnalin, alcohol, acid) ice chest Linear measure (tape, ruler) Maps charts Camera (Polaroid) Scalpels, scissors SCUBA Waders and rubber g’oves Plantton Water bottle for phytopiankton: Van Doni, Net and tow for zooplankton: CThrke-8* us Pimp, filter, and tubing Productivi çy f Pb pplAh [ ton Light and dark bottles Line or rack for bottles Water satler (non-metalllc opaque) Pyrhelt ter Labeled carbonate for radio- carbon method Periphyton Scraper Artificial substrates 4- 7 ------- Macrophnon Crib: ChINA. etc. Fran , or Mits SM I 1M S am SCUM Mr$al photo, iuicludtn X,R. Srab: Peter, than, Smith- N ec lntyre, ShipS Surbar Con salat: Phiagar (Dandy) Nets: tn, trawl, dip Hand screen Artificial substrates hasten md knife Grab Core easier Fish (live) Saint Gill ntt, traal ntt Trap: slat, hoop, tyke Trawl Ei.ctrefts)sfng .quipwit Fish (Sad) Dry ice (as well as chesical preservatives and ice) Hand nat 4-i ------- CHAPTER 5 DAMAGE ASSESSMENT P CEDURCS 5.1 lntrWuction This cha p t er gives guidelines for applying the field investigation to damage asesement, In quantitative teras whenever possible. Damage %ssessmsnt is the miesipement of ha n dons to m n ’s btnefiçIsl usts of a body of water ad its jisediate envlvoment Examples of beneficial use are coaaerciat and sport fishing, recreational boating and swinming, and wlthdra g of water for municipal 0 industrial, or agricultural use. 5.2 Qkj_ectiyu Your objectives are to: • Identify all beneficial isis damaged. Assess the damage to each, in quantitative terms whenever peas ibit. • Identify the damages that are attributable to the spill. • Eliminate other possible causes, or assess their contribution. • Prepare a fully documented report. 5.3 ur Using the information gained during your survey: • Review all mate? uses (see 5.4) which aoply to the spill area, end determine which uare at risk or still are. Determine the types of damage (5.5) to which each water use is liable. • Select the nest quantitative measur nt (5.6) applIcable to each type of djmage. • Continue the field InveatigetiOn accordingly, concentrating en the observations which you have new identified as being inportant. • Review causeS of damage (5.7). Report your assessment of damage (5.8) and its causes. Distinguish clearly between damage (a) directly observed. (b) inferred 1 but not directly observed, and (cJ oredlz-’rj, c-I ------- 5.4 Water Uses NON-WIThDRAWAL USES Fish - connercial, sport #quacu lture - anheals, plants Recreational - boating, swinning SnTHDIthWP& USES k uv i lc inl - d stic, cerciel Industria l - threugh ewnicipal, or fllf-;upplied Agricultura l - irrigation, waterinq stock MISCELLANEOUS USES OF ADJACENT ENVIRONMENT Prooerty in contact with water - structures, beaches Hab itat - man, other organisms Aesthetics Review all uses at risk because of thi spill. DO not let conspicuous damage obscure less obvious but significant harm. Establish a sound reason for each use that Is not to be investiqated. 11 the reason fs not so! V-evident, document It. 5.5 Ijpes off Ji iQ ECONOMIC SPECIES rifled Qua lIty degraded - tainted, toxic Supporting fGgd chain damaged ere 11ng generation damaged I r ma ture organisms damaged RECREATION “an-days of use lost WITHDRAWAL USES ‘ijniclpal and industr ial - supply interrupted, eatri water treatment needed, pr o ce ss or equiMent dimaged Agriculture? - crops or stock damaqed 3eech fouled Structures corroded s - i ------- Examples HABITAT Economic species damaged or driven away Appearance degraded Decide which types of damage require a renorted assessment. If in doubt. include rather than exclude. 5.6 ___ The enphasls is on quantitative measurement. Examples ECONOMIC SPECIES Number killed of each kind Number of degraded quality 1 and severity of degradation Area of damage Duration of delayed da mage through loss of irrnature or breeding organisms Duration of penlstent pollution Number or mass of lost harvest (measured or predicted) RECREATION Mon-days of use restricted or totally den led WITHDRAWAL USES Duration of restricted use or denial Number of items damaged Cost of special water treatment Number or mass of lost harvest PROPERTY Area damaged 1 or number of items Mon-days of use restricted or denied Severity of damage Duration of damage Cost of restoration HABITAT Damage to economic species. etc.. through degradation of habitat rather than direct effect; units of nwasur- ment as above 5.) Causes of Damog4 Establish clearly how tech tyae of observed damage is related to the spilled material. 5—3 ------- • Be specific and quantitathne not 1 Cbanical analyses showed X concentratlorr bfl Samples I through 20 contained S in excess of S mqIl (range 10 to 50 mgI1 . • Review possible causes of daxuage other than the Identified spill. Exam es ire : Han-made causes: thterference with voliase of flow, Inter- ference with stratification. clearing of aquatic weeds, agricultural rurp.off, sediment nm—off, industrial pollution, unrelated spill. Natural cojsesl extnme teiaperettrre or drastic change 4 stolib. ice and snow, decnnpositlon of plant growth 1 altrity charge, spuming ccrtallty, in fectious disease, parasitism. • Be specific in rejecting otter cauSes e.g. If natur a I oxygen deficiency is mi S qtzt 1 use DO analyses from control sonpling stations. • Do not Investigate h ow the spill was caused. unless this is relevant to daftago assessment, 5.8 Essential Contents of OSq nessant — Your damage assessment report may be used as the leading source of lnfonnation for preparinq a court action. it must meet these requirenents: • It mast O3ntaifl all the facu On which the d uage assessment is based 4 gr tall the reader where to find th . tt roust be stiltabTe for rae years after the spill by scoecne cOming to it coid ’, who will need all possible assistance in tracing docunents and witnesses. • It mist be a cleat h istory of wftat happened, bEat was done, decisions and conclizsions reached, and the reasons for all actions. • It tuft cover the followitg areas: Incident - what happened, requiring investigation. Investigat ton - what the damage assessment teat did. Ot lerinforention — who else investigated, where is other information Damage - what kind, how r u t h, what Cause. Damage assessment reports are discussed t iara fully in Chapter 7. Study these closely. Your report is the product that comes from all the ef fort expended in the field. 5-4 ------- a nn 6 BTAT ICTICS 6.3 Introduct i on mi. chapter gives guidelines an the application ci statistics daring the LieU inesttgaUac. It as i a n 4 kacw.Ledga at elatentary stattflics as presented, tar n i* , t t Tninlfl tmak Chemical Anal eee i !2t ! 2t 2!!Aj Section U. t mister of a basic potato is desirable. Nmt statistical methods that flu bs need ate based or the sst tlcn of normal (Gai sian1 distribution cf terrain, with th& f lin bell-taped ctgye of width 68% to within stamtatd din4atio s f the sSsn, g5 neaSard deflrtloes • and 99.St witIUnthrqs. • w r nfl&l-tiatrtbwtis is a2noat eqver a arecis. deacrip- ticer of t d I batEau ,.aY II 4 and ot I s aztnd iâithaitit direct tt%drical proof of it s awIicsbiiity. sc°—r also the distinction between prods ion and acctracyi Prad o -lan Ia the clasenas fltA iditab replicate maaut te ape.. and acc a y 1* the çiosepas at the an aeastirao value t the true flue Caflbrflicb of- iswtn ants, reagente and tadini vea & ld be me.de beftre end after esth Znastigstics as tr as IwactJcal. This Is Ispofloat shene vex data era to be etatiatitel tp enaifled. an wall as for support of a le gally so’.md danaçe top at. take into -the field IxclMea Stuknt s t tables and cSi-equsre tablett and a puekat calculator, lfl tables ar4 aUd puts according to personal preference. 6.2 $e]ettanaM ! nlustion of Plaid tecluitques cu.aat and I$rlyihg any queflitative e Ung or assessment t.otaiqu. requirea kaofla4qe of Its inh e re nt ptecie ion j ncaej use. Pot ezaqile , replicate dreSie sa Lc s of benthie lnvenabnt*s flea dii forest cowttg even fror a uniforaly distributea aaatiao. and raplicame titrations of a single ws sample give ditfttet niw. eeflqzeäd with ameericel stiastas of aorancy. base d on your in expestecs and that at othns gsinst which cbçzarvaticna a be tea ted • Sake nla-of—th exits is tee ecti field theertatioaii For . Wup l4 experience might he that three replicate sample b7 a erticulaz tocteique often give values with a toofold nng.. ‘to detnnine saacy and precision of a measiar nt or evaluation ttdqtM frp tcli $ E p4 fla * (rich as a uolatrio titzaticn)s • Pre era a standard solution Cf the substance to be analysed. - Nate several tmpiicat* dutsreinaUona (Ph • caltrulata the n and standard 4efl tioa (8). * 9fl; 5tggp 4 atA_ reference. sranpiss of many pollutants are available through the Rethoda and Performance rvaluation Activity • Analytical Quality Control Laboratory, flA Cincinnati. 6— I ------- The estimated accuracy at the techhique is the difterenc, t .twaen the maa i uneaaund end the f lue value. Pot N determination with atendard deviation S 1 ttia true acc itrap of the datarininatlon i i equal to/or lees theor tit the estimate d IQCUEeCY plus v1Q1 ?or a confidence level of 90* use a t diettibutiun table or rtq. 6 -I, for H— k degrees of freedom to find t at the 10 1 or 0 ,1 proLabs itty level. For N deterniriation with & standard dev atkon B , the ito. yrectsion of the deter m ination is qusl to/or lass than. Vt the eatinet d standard d.vietia (B) ti..e % For a confidence level of 90%, use a chi-squara taste for Il-i degrees of freedom to find the cM-square va lue at the 10% or 0.1 probabIl ity level. Datsr*ine the chi-value before u.s in the fore -na above. ha a genera l rule, and espec ially if theta ii eny posaibility of interference, also thick precision end accuracy wIth a •ts4ard vtepstsd with water (roe the body of water under i .vsstiqati ir. By use of the aSove guidelines, you can determine If y a s i r technique or mothod I . accurate or precise enc.uqh to warrant further field work. Por eneple, era the accuracy and precision at your technique sufficient us ’ Look for la n ge. lirectty attributable to the concentration of eateriel you are meesutlngt Track %he orivenent of the material at thOse C r,ctltratlona? 6.1 f tng?Isri Chapter gives gu Idelines f ar saaptlnq. such at takfnq at least three replica smmplm. each tins ’ et uach station. Using v ita guidance sod your own exjjsriente, a scnjnd uMic iing plan may be sad., but it L i nrceesaflIy tentative until sole, data era avatlebte. tie enry effort to qet quick results; prefer- e L y toll snaiyeua end cuwite, hut preuininety eutteatee will awrw as e n Immediate check on the nlequory of the cieta. Th u is particularly ieçcrtant ‘shenever the reculte are to he statistically analysed later. 6 - 2 ------- 6.4 11 0w Many Samples ? The number of samples required at any station to give a sound average or mean will depend c the elnienesi of agreement b.tween samples. In other words, the degree of •csttsr or the etandar4 deflation. The confidence interval illuitretee the confidence one stay have n the sampling. Por example, aeuume 3 benthic grabs which yield the following macroinvertabrats Diversity Index (D.I.) Values 3.6, 4.2, 3.9. The sample mean is. therefore, equal to 4.0. calculate the sample etsnderd deviation, 5, by j;i::r where N e number of samples or grabs, - the 0.1. of each sample, and X — the sample mean. ln this case, 82 a 0.0434 and S • 0.208 S calculate the sample standard error, 5 j. by 9 e y r— 0.12 From a t distribution table, or Fig. 4—I, find t cc L O S or 0.1 probability level (t 0 • 1 ) with *F’l degrees of freedom Cr— 2.92). Ca lculate (t 0 (Sj) — 12 ,92) (0.12) a 0.4 The confidence interval is theretont 4,0 0.4 It can he said with confidence, that the calculated interval includes the true mean unless a 1 ip 10 chance hoe occurred in the sampling. Next, conaidar the following eat of late for s similar station ’ 3.2, 4.6, and 34 represent the D Iversity I S a values for each of 3 Celoulete the pesple average, a Calculate the •erple etsndsrd deviation, g , as above s 2 — a.sio, S — 0.781 Calculate th e templ. standard error, S , so abovet s - - o.n rind t for sf-l i t • LU 0 ,1. 0.1 Calculate Ct 0 1 ) (Si) a(2.*2) (0.45) • 1.3 In this ee ls, the confidanOe interval is 3.7 1.3 A large confidence interve]. •ey Indicate that adlitionel seatpise are roqu±red. As a general ruiti-of—thuab. the following may be helpful to reduce the weight of a “wild” point’ 1-3 ------- • Tare 5 saaplee it eseh station. • AnaIyn 3 temples and calculat. the confidence inten d. • It the interval La unacceptable, analyse the other 3. • Is the new confidence interval acceptable? Are additional a ee r.quir.d When collecting data •uch as counts of a flub k Ill, test the ad nacy of sampling by making a quick cqlculatioo c 1 the ots4attvs estimate sitar each ss.pLa ares Lu counted. Inspect the rnccneive ustisetes or plot settaflad tota.1 we number countsA . it will be apparent when the eatiaste is at the desired level of precision (e.q•, LOt) end tunhsr counts ire unlikely to shift the total outside this renge. 6.5 Is An C*eervnd Difference dljniftcent ? Assuming a sinimum gf 3 r.plicetiate, test for sign ificant 4Sf fsrence between control and seaple values by the followiag methods Compute t e ( t2 41$E1 where x - simple sveraqe, d s the control or set .stia. N • niflar of samples end - 11 L (X J) 2 where represents the indivtdal sepia tendinga. Find your computed t value for N-i ibgrefl of fra&e at Tlq. 6- i. Xe there a significant difference ta en the atrol end s.eple value? - the 10% probab iLity Leve l IS icetea that the t nlae wi ll be COeeded by chance on ly once every 10 trials, the St level 1 Ia 2Q, etc. • IC the celcutsted t Yalta awc the 10% tate ), tie control and eaepls are oselbjy i 4 i Ulc t!j different. * t value ssceedinq the 5 % level indicates prob4 y ei$nlficsht 4tfferencea, S eacesdtisg the 1% lsvel indicates sly fltent difference s t aaosedlni the 0. 1% level indicates highly signiticant difference tames tie wet ’s .. This method assumes thet the oontml value is ad i tt etibject to statistical variation, suppose that past records on * ivme a i re S ebne I 04 value of 7.40 true literally hundreds of rssdlrqa. Pnlloeirq en ac Id spill, I pit readlnqa were taken near the monitoring station and their values were. 5.15. 5.2Q. and 5.10. 4.-a ------- ( i-d) v51 CtaQuta t • I Where; n aa 3 mean (5.25), *1 • the control or set value (1.40) $ • the number of ia lea (3), cr4 — 1r — (0.102 + + .15 ) 0.0175 Where X represent, the indivtdual pH reading.. • The calculated value of a • Vo.oiis — 0.132 3.15 s’r • t • 0. 312 — 23 • Zn the •xaflle, the t value of 21 St N—I degrees of froedos (3) felt. wel l above the i i probability level end th obuerved dl fference. are stat f Scent. P. variation of th. above ethcd that say be uaed to tan for significant •am. ‘iu ee ot •win ax. tahin at both Stations, conaidire the •tasdard 4.viaUon of such set of data. lies the Diversity Inder data given in the e ,sai le. on page 6—1, end test for significant differences between the two Sample aeena, Pox one sat of data, a .Ø434. Th other sit of data, * 4 S 0. 5 10. Calculate the average saufle etandard deviation, by 2 2 1 +8 4 a 0.327 2 • Calculat e the average le w iS standard error equated, a 9. 2 ? • 0.309 N (N • fb i number of sawlee taken a each itati n s) Calculate the ee la standard error for the difference, a • 2 (0 . 109 ) a 0.419 X 6 — 3 ------- • then S— — 0 ,467 2 • Compute t byt t — X 1 X 2 — 4.0-3 ,7 — 0. 4 8— — 0.467 xi—x 2 • VInd your confidence level from Yiq. 6-i uair.q 2CN -L • 4 daqreee of treadoa anti the computed t value. • The t velue tills below the lOt level indicatinq that the difference between the two eemple mean. is probably not signif icant. t. 6 ! l iteq uirementn Rst’er to Chapter 7 which givee general quideitnak. typical qucetiuni which may cone up i ii the etatititical area Cret + Were ooncerttrattons actually above a certain level, much as e published -rr or local wetn qua lity etusderd? The variability here is in sa pling and snelysla , Date aunt be adequate to show statistically siqnificent exaefl abous the given limit. • fete concentrations in enisal and plant tissue due to the spill and above toaLc threshoLd? The addition al (actor here is the wide natural variation in uptaKe between apçatently si’tlu tndlvjduaiet Renqe. of :l or 5 Tl flU not unconarin in half e dozen epecisne. The lepottanca Qf adequate Cc rt I eperinne is very clear. Were eem)?le area teupreeentetivo? kaMnalse areas to avoid uncos.scinus hiee Wherever poceibie. do not let convenience of access influence eclection of etetione. Was en adequate total nuP4iet cOuntade More zLqorous treatsent of the cumulstive-eetlmate criterion, reuc ended above, viii give a ntseii&a1 value for the confidence limits. 6.7 Pr.j fllfl atie4{cal tvSOez}ce vinal statistical analyeie and presentation of etetl.atlcel evidence is hen dun Ly a ntatietieian. There era two pitfefle wtttch may L a tie taase cn winch evidence is questiunsti, end which tile field thvntiqitor should bear in mind The Italidard St ItLtiOal tests of hypothesis drtlôeate t 1 chi-eqare, F, and ana lysis of variancel are el i based on the e*sua ’tion that the underlying meaeure*ente follow the nornel dlstfshutir?n An el esdy indicated, the applicability of these to r t7. l f t...’atanA say have n be demonetrat.el Ly statistical ergts.’u ‘.. ------- • A ksy vulnerability of t •ts La that thsy at. qu4te sensitive to individual image deviations rOIE the seer’ (e.g., “wilds rea4ifl9a, locally severe fluctuation., stc.} at other deviatio n in tha tails frost hi as susts normal distribution. Zn order to preclude the ponib iltty of statistical evidartge ba L t i c invalidated in noun on this basis, it is wall WurthwhL].e pereoraing dif ferent . r n. ot statistical uiqnitjcance, Measly, d iatributionireQ tins. These tests are ossad on no t priori assumptions of widsrlyirig dlstribut-ionsj they era typically concerned with medians in place of Sesni (as a measure of central tendency) en ’! inter—p.rcentilu ranges in piaos of standard deviation (a. a Sa e sure of variabi lity). Thea. measures s i c more Stabl, or 5 robust” in thu presence of data anossliss. Ftjrthsrmoce, they are ociq.utationally .i io and ebis to d1sc jmjnats alqnlticar,t differences almost as well a norma l t i ltS . particularly for the nail sample sites typical in damage asj 5 asaant. lioweve;, because thus, test. are, not as widely taught and standardized a the typical normal. tens, it is important to have thas applied by 4 thoroughly qualified statistiulen. $upposs one has a set of data that are suepactad of varying frost nor m a l die- t.rIhut4o,j. What can otis do? rout atternativss appear opern 1.. taste bassd upon thu assumption of normality, svsn though thu aususip- tion is suspecit. Ottsii this epprosiimation I a eduquste. For tsst.inq htea s, thu Central Limit Theorem assures una that the distribution approaches normality as sample size increases. Tranafote the date to a form that more nearly approximates normalitY. Ue. Logari has of th, data, for example. • Analyze the theoretical situation to decide whether some specific d l a- tribution applies. ma exponential distribution, for example. • list nonpsremetric tests, slier. no assumptions are made about the distribu- tion, other thin it be continuous. 6.S Nonj fl ic8tatiattcal Tests All of the tests discusaed thus tar -—with the szcsption of the chi-squart teNt-assuetsd that the underlying distribution was normally distributed, they W I(O j5 cc I w nly k nown 45 l iaramatric teats; e.g.. the normal distribution has tW O peramutsia, the mean an’! standard deviation. in order that confidence can be 1-laco d in any jrnbah)iity atetement obtained by the ttest or the P-teat, the tJLi;)wi 1 ji4 conditions must ha satisfied’ • Thu obssrvations must be independent, as defined previously for random s apl ing. • sanwie ubsarvatiofti must La drawn true a r)rmally—distrthutea population. 6-7 ------- • The populations under investigation must have the came vsriencse. • The variable. involved moat have bean meoured on, at lent, an interval scale, so that it is possible to use arithmetic operations on the values obtained. • For the F-test the meant from the normal ‘and hoa qeneoue) populations must be linear combinations of the effects being studied-—a c that the effects under evaluation are additive. Biological and microbiological data normally do not have data measured on interval scald. Water quality data usually does not have the equal-variances nor the hosugeneou. populations required above. Zn previous teat ., the population was aasueed normal. Population parameters were compared to determine whether two or more populattone are idantloel. In non- parametric tests, the entire distributione are ix mptrsd , rather tham say character- istic parameters. Because these tests require no knowledge about the distribution of the underlying population, they are also referred to as diatribqttoa-free tests Probability charts, or graphs, are a highly efficieat method Of testing distribution assumptions. This results primarily because moe ía plotting the cumulative distribution function which swear. as s straight line on the probability graph. Failure to obtain a straight line can result from , • An incorrect choice of the expected distribution form. • t4on—linearitie. caused by non-random sampling. Non-linearities caused by truncation resulting from Inap.cttom, selection, or other kinds of screening of data. “Wild” points, usually indicating errors hi obtaining or recording of darn. Each of the above categories results in rather consistent pattern. on probability plots. Visual examination of a probability plot, therefore is an easy teat for cons istency of sampla data and of the underly ing etatletics l antwt Sob. about sampling and the validity of observed date. 6.9 ! Qa!!4 _ P Procedwes bince all measuring equipment list limited accuracy, the metsstasente are alec of limited accuracy and thus consist of numbers which have been roirded off , e.g., if an instrument is accurate to tenths of minutes and a time maaauremeat ia 12.2 minute., the time may actually lava been eny valu, between 12.15 and 12.43 minutes. When test date are used to cOmputa test item charecteristice, such aa the mssn and standard deviation, the results •ust be consistent with the original dstai i.e., the mean bivereity Index values cannot be re eccurete than the indi- vidual values used to compute the mean. The following are e bade n4ee concerning significant figures and the rounding of date ’ ‘-a ------- • Significant figures (significant digits) are the digits of a ni.sbfl that begins with the tint digit on the extreme lift that is not a 5eVO and that end with the list digit on the right that is not a Is le or that is a sero which is considered accurate. For ekifl$ej 12304 h as five significant digits. 1.0200 has five significant digits. .0003 has one significant digit. 5200 has t , thrse. or four significant digits depending on Whether UI. instrument said to obtain this masaurement is accurate to hundreds, tans, or units, respectively. 100.0 has four iignificant figur.u. (When a number ends with a mere which ii on the right of the decimal pOLnt the sero it significant.) n . result i t series at aritk*mstic operations siet be rounded off tO en accuracy aeneistent with the least accurata asureaent in the original data. The generally reoaaended procedure is to taS TY et seat two extra lignif Leant digits throughout the oo utations before rcundisw off the fInal result. (If a calculator is uaed to t the Q0t4)utetkOfla , the significa figures will depend on the capacity of the calcu lator .) Seam numbers are considered totally accurate due to the feat that they are not the rseult of a measurement, and thus they do not limit the number of aiqnitica t digits in the final result: e.g. degrees of freedom (d. C . ) . required or desired significance levels. Values taken from tables are eccurata only to the number of digits given in the table. I n re aoting superftuo’ne and inaccurate tigursi, intresee by I the last figure if the following rejected figure is 5 or over. 6-9 ------- Figure 6-1 Graphic Display of Studenis Table I 10 9 8 4 3 15 ‘4 3 1 2 N 6-10 ------- CUAPflR ICPOWVING AND LEGAL REQUIREMENTS 7.1 Introduction This Chapter Se for use durinq a field assignment, to rewind you the apeci requsre nts for a damage saeeaiment report that may be Used in legat PZOcesdinge. tt is only for thisi it is not a textbook of Scientific and legal requirements, not is it a tuids o tha preparation of a Your inve .tjg jon and npoxt may be discredited even though you do CO1npetq job by ordinary staj dards. Question . like these ny be °fledi ta i possible we e accidentally interchanged? CQu 15 tiave Scc4dental ly conteminated* Sa mp le with the chemical that w .a found later by analysis? what proof is there ttl4t th i a photograph Was tAken Wh et 5 and when you say? Why ti this vbser tton in the typed tep bu not in the otiginai fleW n ote s? wbst if fort was tsede to check this eyen,5j 5 sg story) The preservative added to the tamplest was it checked for a senc of the pollutant fcmun4 by analysi s ) Why 414 you not Use Of the PtOC&durss in an EPA manual or the latest edition of Standna f%thode? Failure to have an a4equats viewer for Just one Such question e y we afl the v& ,ue of your report, or destroy it entirely. BCiUfltjfjq The emmiphnis is On nformity with standard practice, consistency of method SM solidity of supporting facts for every statement and con - Ask than key questionus Are Your methods and equipment approved in every d.tiil by EPA er another recoqnia.4 authority? It not, ar. they tech- nically defensible? • WOuld they be Acceptable tO the majority of independent experts? • If there is another schoo l ef thought, would iti experts never- thetess &flfl that yo methods have wids acceptance? Is there scUd support fog every reported Observation and C oflOlusion? ..g., written evidence, preserved •asnples, authenticated photo5raphe) 1 — 1 ------- • Does the etatieticel validity of observation. meet generally acceptable standards? • Are there expressions of opinion which could have been supported by evidence but are not? (Omit them, or stats clearly that they are unsupported opinione 4 7.3 legaL R quLremente The emphasis is on ability to eupport every statement in the noet direct end unequivocal way that is reasonably practical, by such mean as first—hind witness original recorde made at the time of observation and labeling of samples that cannot be accidentally interchanged. Aak these key questions: * Are samples rigorously id.ntif Led as to origin? Have samples been rigorously protected from substitution, alteration, or tampering throughout your custody ot them? Were they adequately seated? • Are notebooks of original and iaediat.e records ava41ab e (as far U practical)? Have reoords been protected from confusion and loss? • Have other items of evidence been similarly id.ntifie4 end protected? • Is there docaentary evidence of every transfer of samp lea etc., from you to another custodian? 7.4 Jhü s titee for meeting the sciantific end legal requirements are given together her., bgcauae they overlap. 4sntifica tApn Attach identification to objects at the earliest opçaortunity. For exaple, lebel samples isediately as they are taken; title, sign and date Polaroid photographs at aces include date/place card in other photographs if possible. Always include nasa and addresses of i#tnsesee who can teetify to origin and authenticity. 7-2 ------- mnsure that identification cannot become blurred, lost, or interchanged, Plan methods and details of identification as pert of the plan or investigation. Make certain that every piece of evidence can be identS f ted with the incident from which it on. Make certain that there is no possibility of confusion. e.g., it there is i cr. than one “Sample lice. I” . each must cagry a difletent date, station nuSnr, etc., on the tate 111341 se the staple number. • Ensure that eeaplse are always under observation or locked up. • teep wrtttsn records of who has custody at alt t i res, and Of all transfers of custody. Minimise thu ntmtbet of custodiane I every one say be celled on as a witness. • Attach a trensfer tag to •e ’Qlue when practical, and fill in the tag with the required information, includingi (1) Crigina- tore name. Østs of origin, name of next custodian, date of transfer: (2) Name of custodian, date C l ! receipt, how received (by hand, mail. etc.). name of next custodian, data of transfer. There mould be several ethtLa c spaces (or further oustodiane. • Control keys carefully. Unless there is good reason othsrwiae, have one set only, held by the aneeument team leader. Sasg,lee tact i medistely, in accordance with the instructione under [ dsntificatiofl . for exaaple, U e S Waterproof adhesive lsbelp cia not ii grease pencil on outside: do r iot label l.nterchangeeble screw cape. • Seal to protect from tna4vertent contamination : e.g. • with tape over cap. • Label should carry Cs) Identification ntxter, tying that sample in with the relevant notebook entry, (b) Incident identification e.g., name of water body), Cc) Printed n of sampler end 1A signature and date. These must be on every sample. ‘—. 3 ------- • Indicate preservative d4od or storage conditions required; 5.9., TMj Ø% t tmalin , keep refrignsts4’ This informa- tion may be Qfl the outer coptainfl for a nuitar of samples if they wili raraa l]y I a stand 15% tide OO***LSt. • Retain samples after snalysis (or diçUests samples) whenever they would be sabie later as supporting vidtncsr sq., prs- served organisms wstsx aa4lsi with stable chemical pClI.utant. • U e a bound notebook (not spiral lcwid vith nqmsutsally numbered pages. Go not use Locerisaf, ate, • Never take notes on taratdb pS or o*1 sor m of paper. * Make notes at the tin or earliest cçpottunlty thareMtar. Keep ad q1na flItGk eflfl 1 * alflAet4) teanoript. g typed copies have b en aad. • Make motes cbtanetoqtoalIy os t U as possible. Close Gut each day with a Line 1 data, an d imit ish Croa any gaps with two diagonal. ithes. • Do not disnapt the sequentJai aabnthq by 10a5vtn9 fles from the notebook. Field obnrwati.na and snpitn rsaogda sat be siqned on the Npota end oountaraiqad U there is a n *d witness. • Laboratory raciords most be .Içst b the a wøs dAd the worK 4cr by %3t l a t i n of a • Laboratory records shuul4 cbe d (pcetenbty by the assessment team jeiderl fo .rittmetical accuracy, cvrrect transfer of dot. to y%d*. nqpA.taosn, Legib4Llty aid fleetness. The record must clear i i ) S4entfl all evidence which is physically separatej sal.si. annotated saps, phategraphe, eta. Ewdi. *t these J daa of SUsan. sat carry its own identi tio.Uo* aiW autbariticatsa. 7.5 Essential C2onta fl p J gpe Msenae ertJ etM k decays report I t t 7-4 ------- 1. tltitory of the investigation, and guide to what •vid.nce exists m M wber.i • What was don. sad why. • What ware the r.suitj, • Who n ra the investigators. • What ev Idence exists. • w ow to track down all witnesses, records and physical evidence. 2. HisS. for afls.ing Costs Cf damage. 3. vast . for pupating court action. 4 • Quldance for improved damage assessment protSurn. A damage report IS !C1’P I. Intended for COuntoXflasUrSe, ret teratton, Or enforcement + 2. A oozrpitation of all available information about an inciderttr it may eusarin, end titer to other s oro detailed source.. 3. An aiees nt of daM n in doflar va lues. An outline of what should be in a damage assessment report is givan below. mere are four main headings i INC I IaT - What happ. d 1WVUTI T1(Ai - flat the tea did DAMA C - what damage Was found CAUSE - flat was tin mediate ca u se Is, this outline i i a checklist for pinning and conducting a field Anvntz,ation, arid a tnt So : the ccsp ietsn.fl of ynur repart It may also be used as a guide fox drawing tç prooeduras, snsttuetiane, and report- thy forms. INC IDENT Spill reported Date tie. Plaoe Material Quantity 7— 5 ------- Damage reported Date Time P la ce Nature . (in brief) INVESTIGATION Aseeseor we informed Date Time of . (affiliation) f l ow Investigation began Date Time ended Date Dime Report written Date Assessment team leader Name of Address Phone Field location (if still there) Assessment ten Nate of Addre.e.e etc. if different from teas lead.r On-Scant coordinator Neat of Address Phone Field location Other of ficiale at sits Names of Addreeeee Phonee rield locations Witnesses Ne s s Address phone ) for each one Witness 7-6 ------- First obaervationa4 results of the survey (Chapter l}, and basis for plan of investigation. pats Di et. Water appearance: body surface bottoa Spot tests of water quality Water state (flow, tide) Damago: living things extent Damage: other ext ent Weather (during survey) O’-’erall plan (briufly) Weather report : froa before spi ll to end of investigation; at arias essential features and note where detailed records are. At tint Between spill and 54 _ s !rveY _ iI& IY I UUWSEY Air temperature Max Bin Water temperature Max Bin Precipitation (Total) Wind speed . Wind dir.ction Sun Sourcu and location of weather recordui (SWWU } P sram ete afl v tion of original Wind 140M/NWS Weather StaUon at XYt tAtA _ Ons a table of numerical identi fication, location description, and typee of iapl. taken. (EXASLE) Station ntwftieri Types of corresponds with sample map or skei thno. flJiOP De!c !J p%ign tkn 13 50 ft tçstrea Shallow Blnthoa of WMG BRXDCE* riffle (Surb.r) 6 ft trots SE bank Water TranSect Mo. 2 Sand Oiled birds (*nt 3(Y)J Oil high tide mark 7—7 ------- Asisyant maps aret (a .ttsch.d CS) avaiiabl. at Ui.tor of inv.sttgattont a narrative Mint be cceptt.d whit. the work is 9oinq oni a suitable format ta £ brief diary, attached U Annas A to tha nport. It is essential to sake each day’s entries againet a standard sot of headingut sq., s tesj tssrvettons laboratory workj activit ies, reasons (what. not ctvioua) P± i J q ton Nay 6 Staples bentho. No. 37-fl. Water No. 10-2 5 Observations Photos No. 15-25 Lab. work Qualitativ, analysts of benthos stapLe. No. 1-36 , Sh ippId water s 3.s No. 1- 15 to X II Lab. Activities Weather records studied at kit AS rport Reasons Nay 9 Staples Won. Observations Photos No. 26-3%. Aer iaL £.t. photos No. i-tO Lab work *uotitatSve ana lysis of benthot staples No. 37—7*, Sh ipped beathos esapiss Ito. 1—34 to sac . Activities Conferenc, with USC on scope end duration of dasjs tnnatn, as. .sa, Anon to St Al. dated Nay 9 Reasons Saaplinq suspended to avoid snter- (stance with cleagnj restart Nay 10. Aerial l. a. for dosaqe to sar ah qrses, repast on or abo ut stats 9. ma following categories are those eon likely to appear in dasaga reportsi Aquatic orqantsn - bsnthoe, p.riphyton p isnktce , sacraphyton ’ fish and other nekt t IntarUdal organis Inshore organine Pftnn recreation and tivtnq uses - water co ntact, na sa La, structures, beaches Withdrawal us•s - eunicipel. industrial, aqrirultural toes ssaapies follow. 7- s ------- I EflMPLI) Damag, to fish. Extent (area) of Ji nX Nm, measured Ssvsrity . (Light, d., heavy, total) Duration of kiL l. I*s4 fishi species ..... s in ..... ntflar appearance (skin, fins, jillu , internaJj 14.vSng affected fish; bahavoic species size ntfl r TotaL dnd by category game . . . .. oomeercitl other a c • °• Sttion No. rtptjon !S 1 1 Kind ..... To Near By Presirvn ... On (Ewerz) Daznags to banthos. Report, for each sa Ling ststionc Station No fl . aa Le6 P later of sa’wi.s Bus of uaai 1ss total organisnm ..... total tans Bach tactic name ..... nzsflr Unusual distribution • population, antajity, stc..... IJUJOLI) Osasags to Pusan recreation and Uving uses i less standardised format than previous ex ies, be as quantitative a. possibtes us. ph.otoqrapha, fletches signed statements stc. whenever practical. Things to report include; What ttructurfl, etc. Location ..... Severity txtsnt ..... Duration Type of damaqe Aotivs restoration Natural restoration Occupancy affected Offense to ssnsn (eels, smell) sacreation effected swising • . boating . fishing 7-, ------- (EXN4PLE) Dantaqe to withdrawal uses. Uses aftectedt identify within each grouçn munIcipa 1 industrial agricultural other unw atfectbdl damage dani 1 of use duration of denial .,... treatment needed •.... cost CAUSE oP DAMAGE Report on the iuwtadiate cause of each major category of damage. Present the specific evidence, and show where it i . to be found. Damage to was caused by substance (!KA*LE) Evidence ationo f evidence Water sample No. 123r Fit. No. 01,. flZ lab. x mg/i of Z Patttol. report No. 4% fl It No. AbC tab. Positive identificatiun of substance st ported by OR rreswnptive identification of substance supported by OR No identification of elatancei .*ptain Alternative causes of daaage specificaUy excluded 1 i evidence 2 evidence ------- APPENDIX A DICTZONARY OP HAZARDOUS POLWT INC SUBSTANCES Each substance is entered under one generally used name. The entries are in alphabetical order. The names, and a large number of synonym. for then, are included in the Cross Index, Appendix B. To find data for sept11 [ f the spilled substance is known by name, start at the Cross Index, if it is not found, it may be becaus, the name is an unusual synonym or trade name. Proceed a. for en unknown spilt. If the spilled substance is not known, use the Categorisation, Appendix C, to find which entries most likely include the spill. Using the data These ire some ways in which the Dictionary can be used: Chemical formula — A chemist can use this to aià tIly till description and detection data. y onyms - Use these if there is a cosnunication problem and someone does not recognise a a particular name for the spill. Des cr&ptiofl - Use to predict damages e.g., if the spill is htavier than water and not highly soluble, bottom life is especially at risk. Use tO help identificstion of an unknown spills check the description against observa- tions made at the site. Toxio 4y - the toxicity ratings aret High; toxic threshold below 10 ppm Medium: texic threshold between Lb and 500 ppm Lows toxic threshold above 500 ppm Use the human effects to estimate safety hasards. Th. local toxicity La innediate effect on flit ,, eyes, mucous membranes, or reipirating tract. The systemic toxicity is poisoning by inhalation 1 s wa t I B lng ior skin absorption. Use the human effects in damage assessment. Use the aquatto toxicity as a guide to biological damag. that may be expect.dy as a check that tb - served effect. agree with the identification of A- 1 ------- the spill; ond in deterinininq cause of damage. Preeautionn - Jnrjtruct your team, and advise others as rece#sarv. Make certtjr the kFtI- 1ItAp L fur the naterlni. I’roteeti,e elc tiitng inclale ye prcte’ t Li. Detection - Read Chapter 2 of the Manual for a5vTce on selection And U S C of detection methods. Use the ratings (below) to decide wheth..tr detection and identification are ratisfactory for your field operation. The detection methods are rated by number In parentheses. The ratings are: 1. For gross detection or presumptive Identi ficetion. 2. For fairly specific identification. 3. Versatility hiqh; detects a broad cla ss of hazardous substances. 4. Versatility medium; detects several hazardous substancen 5. VersatIlity tow; detects few hazardous substances. 6. senuitive test; detects at thri: Fin1d toxic CflnCeritratLOfl. Cautions and Guidelines General — The Dictinnary Is Intended for a trained sctentist, who understands that data are not always complete and consistent. Description, toxicity, and detection may all be different from the data qiven here, which apply only to the more uinial conditions. Synonyrns - There are many other tens familiar trade names, etc., for some of the substaneta. Descr4ption - t utu In for the more conion forms of eac h substance, The spill may contaIn unusual impurittes, or be a eonaerctal mixture with other chemica ls. - These are the least precise data, be- cause the experimental conditions may have differed widely from the circumstances of the spill and the llvinq things at risk. A ratlnq of “Los” tox icity Is good for the general run of incidents,, but does not exclude a hitjhly toxic effect in epectal cIrcumstances. ------- Precautions - This is not an authoritative s i lty manual; the recommendations are advisory guidelines. Detection — The recommended tests are good for tingle substances in generally clean condi- tions, and common interfering reactions are noted; U the spill is a mixture, or the receiving water is highly polluted, false readings are possible. A-) ------- ABIETIC ACID C 19 H 29 C00H (phenanthrene ring stncture Synonyms: Sylvic Acid Description: Derived from pin. rosin , of which it is the principal active ingredient. YeUowish, resinous powder. (Sink.); Insoluble. Toxicity : Local - Moderately Irritant. Systemic - Moderate. MuaUc - Moderate Other - Promotes growth of several types of lactic acid and butyric acid bacteria. Detections Prepar, a solution (approximately 1%) of bromine in carbon tetrachioride; add a few drops to 2 nil of oemple. Positive resu1t the color of bromine disappears. Un- saturated organic compounds interfere, The powder of abietic acid may be diesolved In an organic solvent alcohol, bensene, etc.), then tested with bromine; figs is a uceful test for •edivnent samples. (1, 4). instrumental analysis: Uv, (1,4 .6). ------- ACETALDEHYDE H 3 UCHO Synonyms: Acetic aldehyde. aldehyde, ethanal , ethylaldehyde, paraldehyde. Description : Very flammable, clear, colorless, liquid. Characteristic pun aent odor that bmells like (tuft In extreme dilution (Zppmj. Explosive vapor. CompletelY miscible. Toxicity: Local - Both liquid and vapor irritate eyes, mucous membranes 1 and skin. Systemic - Slight to moderate; large doses of vapor can cause respiratory coUapse. Aquatic - Moderately toxic to fish, invertebrates, flora. PROTECTIVE CLOTHING AND RESPIRATOR ADVISABLE. Detection: Commercial detectors are available; sensitivity range is 25 - lOGO ppm. Supplier. inclt de MSA (1 or 2 - - depending on kit - - and 5). ------- ACETAM WE CFI 3 C.O(Nh i 2 Synonynkst Acetic acid amine, ethanamicte. Description; Colorless del4uesceflt soUd . Slight odor. Sinks and dissolves. Toxicity: Local - MUd irritant. Systemi c - Low. Aquatic - Low. Other - Increases SOD. Detection: (1). Mix sample with 16. 4% hydroxylarrtine sulfate in 14% sodium hydroxide solution. (2). Acidify with HCI. (3). Add everSl drops of 20% ferr lc ch1or de solution. Positive result: solution (3) turns green in a few minutes. (1,5,6). ------- ACETANILIDE C 6 H 5 NR(C:OCH 3 ) Synonyms: N- Phenylacetamide. Descriptton Shiny white solid (leaflets or powder). Odorless. Stable in air. Slightly burning taste. Sinks slowly dissolves. Toxlcity Local. - May be mild irritant. Systemic - Low to moderate. Aquatic - Low to mode rate. DetecUon: See ACETAMIDE (l 5,6). ------- ACETIC ACID 11 3 CCOOH Synonyms: Ethanoic acid, glacial acetic acid, vinegar. Description: Clear, colorless liquid. Freezes at 62°F (concen- trated solution). Odor of vinegar. Acid to litmus. Reacts with many minerals to produce metal acetatse and mineral acid.. Look for corrosion 1 SOD, and pH effects. Completely miscible. Toxicity; Local - Irritant vapors; concentrated solutions can burn eyes, mucous membranes, skin. Systemic - Dilute solutions are nontoxic: concentrated solutions can burn and corrod.e tissues. Aquatic - Dilute solution. are practically harmless; concentrated solutions are corrosive and can severely damage aquatic life. Damage varies with pH . Other - Dilute solutions can create a SOD problem. Detection: (I). High concentrations of any acid or base may be detected with a pH meter or pH indicator paper (e.g. litmus). (1,3). (Ii ). Test sample with solution of 5% lanthanum nitrate and 0. O1N iodine. Positive result, dark blue precipitate or solution. (1, 5,6). ------- ACETIC ANHYDRIDE (H 3 CC:O) 4 O Synonyms: Acetic oxide, acetyl oxide. Descrlptton: Very refractive liquid. Strong odor of vinegar. Fire hazard Burns readily. Sinks in water, slowly forming ACETIC ACID. Look for corrosion, pH, and BOD effect.. Toxicity: Local Both liquid and vapor are violently irritating and corrosive to eyes, mucous membranes, and skin. Systemic - Burn, and corrodes tissues. See ACITIC ACID for other effects. Aquatic - Corrosive and toxic to aU aquatic life; for toxicity of dilute solutions, see ACETIC ACIP’ Detection: See ACETIC ACID. ------- ACETONE CYANOHYDRIN (CH 3 ) 2 C(OH)CN Synonyms: M ethylac etonitrile , hydroxytsobutyronitrile. Description; Colorless liquid. Floats and readily dissolve.. Decomposes readily to yield HYDROCYAN1C ACID (liquid and vapor , depending on temperature) which is one of the moat toxic substances known. Toxicity: Local - May slightly irritate eyes, akin, mucous membranes. Systemic - See HYDROCYANIC ACID; extremely toxic. Aquatic - See HYDROCYANZC ACID; extremely toxic. WEAR RESPIRATOR; PROTECTIVE CLOTHING ADVISABLE. Detection: ( I). Use only in a well-circulated hood - - extremely toxic hydrogen cyanide gas is evolved. Mix small volume of sample with 3M NC !; test with commercial cyanide kit (see BARIUM CYANIDE). If test is unclear, repeat, using a larger volume of sample. (II). Place 2 drops of sample in a micro test tube with 2 drops of dilute H 2 504. Immediately cover the mouth of the test tube with a disk of filter paper moistened with a drop of the reagent, which is made by mixing equal volumes of solution A and solution B j before use . Solution A ii 2. 86 g copper acetate in 1 liter of water. Solution B contains 675 ml of saturated benzldine acetate solution plus 525 ml of water. Positive result: the reagent paper turns blue. (1, 5). ------- ACETONITPJLE H 3 CCN Synonyms: Cyanomethane ethanenitrile, methyl cyanide. Description: Colorless liquid. Sweet odor, much like ether. Floats and dissolves. Flammable; explosive vapors , to xicity: Local - May irritate skin. Systemic - Low to moderate; avoid breathing the vapors. Aquatic - kow. RESPIRATOR ADVISABLE. Detection: Commercial liquid and vapor detector kits are available; sensitivity range is 10 - 200 ppm. Suppliers include MSA. Warm samples before using vapor detectors. (1 5, 6). ------- ACETOP}IENONE C 6 H 5 COC H 3 Synonyms: Acetylbenzene, hypnone, phenyl methyl ketone. Description: Colorless liquid that freezes at 68°F. Odor of orange blossoms. Sinks; slightly soluble. Toxicity: Human and Aquatic - Practically none. Hypnotic in high concentrations. Detection: Mix sample with a saturated solution of 1, 4-dinitro- phenylhydrazine in ZN HC1. Positive result: precipitate. (1, 5, 6). ------- ACETYL BROMIDE H 3 CCOSr Synonyms; none common. Description: Colorless, Luming Uquid. Sinks, but is violently decomposed by water to yield ACETIC ACID and hydrobromic acid. Clouds of acrid fumes may develop. Toxicity; Local - Intensely Irritating to eyes, mucous membranes, and skin. Systemic - See ACETIC ACID; hydrobromic acid is very corrosive in concentrated solution; dilute solutions (10% or less) are sedatives. Aquatic - See ACETIC ACID; the bromide ion is very toxic to many microflora, invertebrates, and fish. Other - Look for corrosion and pH effects. WEAR RESP ULATOR AND PROTECTIVE CLOTHING IN REACTION ZONE AND WHERE pH IS LOW. Detection: Analyze separately for th. hydrolysis product., viz. ACETIC ACID and hydrobromic acid. See ACETIC ACID for detection method. Use pH indicator paper or meter to test for acid. (1 . 3). Then test for bromide ion as foUows. In a test tube 1 mix 1 ml of sample with 0. 2 g PbO 2 and I ml of ZN acetic acid. Cover mouth of test tube with filter paper that ha. been impregnated with a saturated solution of fluorescein i,i 1:1 ethanol. Positive result: filter paper turns red. lodides inter- fere. (1 .4). ------- ACETYLENE HCCH Synonyms: Etbine ethyne. Deucriptiont Colorless gas; ethereal odor when pure, but disagreeable odor when impure. Very flammable; the compressed gas is explosive. Slightly soluble. Toxicity: Local - None. Systemic - A simple asphyxiant; high concentrations of inhaled gas are narcotic. Aquatic - None to low. Detection: Commercial liquid and vapor detector kits are available; sensitivity range is 3 - 3000 ppm. Suppliers include MSA, Scottlflavis 1 and Kitagawa. (2 ,5 ,6). ------- ACRIDINE C 13 H 9 N (tricyclic) Synonyms: Azaanthracene, dibensopyridine. Description: Caloriess crystalline solid. Sinks; nearly Insoluble. Weakly basic; colors litmus blue. Toxicity: Local - Strong irritant to skin and mucous membraneS ’ Systemic - Low. Aquatic - Reports vary from very low to very high. Highly toxic to some fish. Detection: Acidify sample With 3M 1-ICI. Positive result: yellow precipitate. (14). ------- ACRYLIC ACID H 2 C:CHCQOH Synonyms: Propenoic acid, vinylformic acid. Description: Corrosive, fuming liquid. Acrid odor. Just sinks; miscible with water. Polymerizes readily In the presence of oxygen, but polymerization inhibitors (such as FLYDROQUINONE) are often added; the polymer is a clear plastic. Toxicity: Local - Strongly irritating. Systemic - Low. Aquatic - Moderate to low. Detection: Mix sample with 5 ml of 4. 4% mercuric acetate and 0. 5% acetic acid in 6:4 water-dioxane solution. Positive result: precipitate, which redis solves when mixed with 30 ml of 0. OZM EDTA solution. (1, 5). ------- ACRYLONITRILE H 2 C:CHCN S ynoriymn; C yanoethylene, Funiigr sin, propertenit rile, V entox, vinyl cyanide. Description: Explosive, flarnniable, volatile liquid. Colorless when fresh; may slowly turn yellow in Light. Slight biting odor. May polymerize spontaneously in light. Floats. Evaporates quickly, dissolves slowly. Toxicity: Local - Extremely irritating vapor. Systemic - Moderate to high; similar to HYDROCYAN I 0 ACID. Aquatic - Moderate to high. WEAR RESPJItATOR AND PROTECTIVE CLOTHING. Detection: Commercial liquid and vapor detector kits are available; sensitivity range is 5 - 500 ppm. Suppliers include MSA, Scott/Davis, and iCitagawa. ------- ADIPiC ACID HOOC(CH 2 ) 4 COOH Synonyms Butanedi car boxylic acid, hexanedioic acid. flescriptiom Colorless 3o1 d that sinks and slowly diuiolves in water 1 Acid to litmus. Toxicity: Human - Slight, ii any. kqtaatic - Moderate. Othcr - Look for 30D effect in still water. Detection: No satisfactory method for detection at water’s edge. (1). For improvised field laboratory (e. g. in. motel rcom, with equipment available), esterify sample, then add p-nltrobenzyl chloride to ester. Heat sample. Positiv, result: an in- soluble derivative will slowly form and p m- cipitate from solution. (1, 5). ( Ii). For instrumental analysis in improvised lab, use OC with hydrophobic column packing. (2, 3 6). (111). In arSas of high concentration, test water for acidity with pH indicator paper or pH meter. [ 1, 3). (1V). In very pare water 1 where no other acids or bases of low molecular weight are present in significant quantity, consider using pot.ntiornetric titration with 0. SN MaOH, using thymol blue a. indicator. 2, 3). ------- AD IPONITRILE CN (CH 2 ) 4 CN Synonyms: Adipyl dinitrile, di cyanobutane • t etramethylene cyanide, tetramethylene dicyanide. Description: Colorless liquid; almost no odor. Floats on water, dissolving slowly. Toxicity: Local - Vapor and liquid are mild irritants. Systemic - Moderately toxic by all routes; absorbed through intact skin. Aquatic - Moderate to low. PROTECTiVE CLOTHiNG AND RESPIRATOR ADVISABLE. Detection: No satisfactory method for detection at water’s edge. An improvised motel-room laboratory is the beat on can hope for. The following methods assume at least an improvised laboratory. (I ). Use CC with hydrophobic column. (2, 3,6). (11). (1) Subject sample to vigorous hydrolysis. (2) Render solution basic with NaOH, then heat to liberate AMMONLAIP which may be detected by any of several commercial kits, simple wet-chemical methods, or This method only detects the ammonium salt produced by hydrolysis. (1, S, 6). TO detect the adipic acid moiety, see method I and U under ADIPIC ACID. (Rating will depend on method chosen). ------- ALLYL ALCOHOL H 2 C:CHCH 2 OH Synonym.: Propenol, propenyl alcohol, vinyl carbinol. Description: Colorless flammable liquid. Sharp, biting odor similar to mustard. Floats; completely miscible with water. Toxicity: Local - Very Irritating vapor and liquid. Severe burns. Syste mic - Moderate; burns respiratory tract. Aquatic - Moderate to high. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Mix sample with small amount of silver nitrate. Positive result is a precipitate that redissolves when an excess of concentrated silver nitrate solution is added. (1, 5). ------- ALi 4 YL CHLORIDE H 7 C:CHCH C I Synonyms: AC; ch lorallylene, chioropropene, chioropropylene. De scription: Ciear to strawberry- red liquid. Unpleasant, sweetish odor. Floats on water; s l ight ly soluble. A toxic and explosive layer of vapor farms at tht water’s surface. Very flammable. Toxic.t ty: Loc!tl Strongly irritant vapor and liquid. Systemic - Moderatc’ . Aquatic - Reports vary from very tow to very Ugh. Highly toxic w orne fish. WEAR RESPIRATO? &NJ) P’OTECt\ IC CLCT lUN G, Dt L cHof ,c i’Ld& t.t a.sJ r4 1. Q f/oiai li. ps s,xturattd solutinn U( ii ogiticitx. i r: ciincusjtra rcn H” 1. Pcn#itive res tt kJitl!. tc rnct —vi ;iur., fl, iy. ------- ALUMiNUM FLUORIDE Al F) Synonym: Aluminum trUl’iorIde. Di cription; White solid tinka in water slightly soluble. L sa Lo Uc than othe; fluoridnu becauae of l iw S OL%Sbiltty. To xici ty: J4 CaI - Probably little t<’ nonc. Syitemic ProUably low to moderaL , Aquatic - Moderate to high. F’exit: to 1 4:uit:: and nbnala. l)etrctj n; The aiundnLtm and fluoride components must be detected separately. To detect aluminum, see ALUMINUM SULFATt. Ther. are several commercial kit. for detecting fluoride in concentrations below 10 ppm. Commercial sources at these kit. include Hach Cheznic&. MSA. Scott/D&YiE Lamotte, and lIuflige. (2,5, 6). A eimp e quelitat2ve tnt for fluoride involves a re geat composod 01 0. 5 v alizarin, 200 ml of ethanol 1 and L 5 at zirconyl chloride in one liter of water. ‘flds reagent I reddish purple. Add sample to reagent. Posidve result: mixture ii bleached to a pale straw color, (1, 5). ------- ALUMINUM SULFATE A 1 2 ( 50 4 ) 3 Synonyms: Alumogenite, cake alum, patent alum. Description: Shiny white solid. Sinks and dissolves readily, forming an acid solution. Mildly antiseptic and detergent. Toñclty: Human - Low. Aquatic - Low to moderate. Detection: The aluminum and sulfate components must be separately detected 1 To detect aluminum, add dilute NH 4 CH to sample. Positive result: a gelatinous white precipitate that is insoluble In an excess of NH 4 OH. (l 4,6). Commercial kits are available for detecting sulfate in the range 0 -300 ppm. Mach Chemical is one supplier. (1,4,6) Commercial kits are also available for detecting aluminum; sensitivity range is 0. 02 to 1 ppm. Supplier, include Refuge. (2, 5, 6). There are several commercial kits for detecting sulfate from A to 500 ppm. Suppliers include Mach, He1l,ig ’ and Lamotte. (1,4,6). ------- AMINO ETHYL ETHANOL AMINE H 2 NCH 1 CHzNHCH 2 CH 2 OH Synonym: flydroxyethylethylenediszthns. Description: Clear, colorless hygroscopic liquid with mild ammoniscal odor. Just sinks; dissolves readily, giving a basic solution. Tox icity : Local - Very irritating; may burn skin. Systemic - Low. Aquatic -(Low.) PROTECTIVE CLOTHING ADVISABLE. Detection: there is no specific and sensitive method for use at water’s edge. Test pH in area of concentrated spill, using pH indicator paper or pH m eter {t, 3). Test for alcohol as follows. Combine 2 nil of sample with 5 ml of reagent (a 10% solution of cent emmoniuni nitrate in ZN nitric acid). Positive result: yellow to red solution. (1, 3). Test for secondary amine as follows. Prepare reagent by dissolving 0. 5 g NiCI 2 hexabydrate in 100 ml of water While shaking . add carbon disulfide to slight excess. Just before testing sample, add 2 ml concentrated N$ OH to S nil of re- agent. Then add 2 ml of sample. Positive result: a weu-defined precipitate. (1, 3). ------- AMMONIA NH 3 y4Or1ytfl5 ; ArniflUnia gas, anhydrous ammonia, liquefied ammonia. flencrintion: Color]esi ga. or colorleeN compressed, liquefied gas that dissolves readily i.n water, giving a basic Aolution. The gas, the compressed gas, and the water twlutlon have a characteristic sharp, biting ‘,dor that is noticeable in great dilution. Toxicity: Local - All forms are very irritating to the eyes and mucous membranes: somewhat irritating to s idn . Systemic - Slight. Aquatic - k-itch to moderate. RESPIRATOR MID PROTECTIVE CLOTHINO A L) VISAHLE. Detection: There are several commercial kite for detecting ammonia or the anvnonluxn Ion. Commercial sources include MSA, Scott/Davis, Kitagawa. Lainotte. Flellige, and HaCb sensitivity range is 0. 02-1500 ppm. {Z, 4, 6j. A simple. 1i’ sa senaitive method is to make the sample basic by adding NaCH, than heat to steaming, then test the vapor with wetted pH paper, which should register pH 11, approxI- mately. (1, 4). A more specific method is to mix the sample with Nestler’s reagent (dissolve ZO g of K! and 32 g of Hg! 2 In 200 n i l of water, then add 6O nil of 50% 1 (01 -ft. Positive result: brown precipitate. ------- AMMOrqJu ACETATE H 3 CC0074}1 4 Synonyms: Acedc acid ammon,Ium salt. spirit of Mindererus. Description: White deliquescent solid. Slight odor of vinegar. Sinks; very soluble, giving a colorless solution that is acid to litmus when very concentrated. Tot city: Human - Slight. Aquatic - Moderate. Detection: The arnrnoniurn and acetate components must be separately analyzed. To detect arnmoniuni, see methods under AMMONIA. To detect acetate, test as follows. (1) Check acidity of sample if acid, neutralize with ZnCO 3 . (2) Then add stnreral drops of 0. SM ferric chloride. Positive result: sample solution turns brown when the ferric chloride i added, and a precipitate forms upon beating. Thi p- cyanates , tartrates, and iodide, interfere. (1, 5) . A quick presumptive test is to acidiCy a large quantity of the sample with sulfuric acid, then heat to bciling; positive result lb the odor of vInegar. (I, 5) Alternatively, acidify the sample, then use the lanthanum test for ACETEC ACID. See ACETIC ACID. ------- AMMONIUM CARBQNATZ )thcture of NH 4 HCO 3 and N}{ 4 COONH 2 Synonyms: Crystal ammonia, anunoni urn sesquicarbonate, hartshorn. Description: A mixture of atrirno alum sc14 carbonate (ernrnonium bicarbonate) and arnxnonium carbasnate. White solid that is unstable in air: The carbaniate is converted to the acid carbonate. Strong odor of axnnionia; sharp axnmon.iacal taste. Sinks and dIssolves slowly. Toxicity:. Human - Low. Aquatic - Low to moderate. fletection. The amrnonium and carbonate components must be separately analyzed. See AMMONIA for methods appfl cable to animonluni. To detect carbonate, add dilute HC1 to a large volimie of sample; bubbles of carbon dioxide will form, and heating will increase the rate of its evolution. (1. 5). Several comrnercia) kits are available for detecting CO 2 . Sources include Kitagawa. MSAI and Scott ! Davis. (2,5,6}. ------- AMMONUTh4 CHLORIDE NH 4 C I Synonyms: Amchlor, amnonium muriate, Dararnrnon, sal ammoniac, a airniac. Description: White solid, somewhat bygroscopic. Odorless. Cooling, saline taste. Very soluble in water 1 cooling the water as it dissolves. Slightly acid in solution. Reacts with the alJcaJ.is and their carbonates. Toxicity: Human - Practically none. Muatic - Reports vary from high to moderate. Detection: The ammoniurn and chloride components must be separately analyzed. See AMMONIA for methods applicable to anunonium. Commercial kits are available for chloride detection; sensitivity range is 17 - 1.000 ppm. Suppliers include Rellige. (2.3,6). Alternatively 1 test for chloride as follows. (1) I l ferric yan.ides • ferrocyanides, thiocyanates, bromides 1 or iodidea are significant in the sample, they will inter- fere with the test; remove this interference by boiling the sample with a mixture of ÔM RN0 3 and C. 5M K 2 CrO 4 . (2) Mix sample with 0. SM AgNO 3 ; a white precipitate is positive. (3) Collect precipitate and mix with 6M NH 4 OH; redis solution of precipitate is further positive proof. (4) Acidify solution (3) with 6M HNO 3 ; reprecipitation is further proof. (2,4,6). ------- AMMONIUM C}IROMATE (NH 4 ) 7 CrO 4 Synonym: Neutral ammoniuzn chrornate. De2criptiQn: Yellow crystalline solid. Sinks and dissolves, giving an aLkaLine yellow iolution. Taxi city: Local - Strongly irritating. Systemic - (Low to moderate). Aquatic - Low to moderate. Detection: The ammoniurn and chromate components must be separately analyzed. See AMMONIA for methods applicable to arnmonium. There are several commercial chrontate detectors; sensitivity is 0. 1 600 ppm. Suppliers include Mach, Hellige, Lamotte and Taylor. 12, 4, 6), Alternatively, detect chromsite by either of the following methods. U ) . Neutralize sample. Then add a small quantity of concentrated lead nitrate solution. Posith’S result: bright yellow or orange precipitate. z, s,6 . (U). Acidify sample with 6M HNO- . drop by drop. Then add oquentisily 4 ml of ether and 2 ml of 3% H 2 O 2 Positiv, result: ether layer turns deep blue. Dichromttea also give positive result. (1,5,6). ------- AMMONIUM DICHROMATE Synonym: Ainmonium bichromate Description: Bright scarlet crystalline solid, flammable. Odorlesa. Sinks; very soluble In water, giving a bright orange acidic solution, Toxicity: Local - Strong irritant may ulcerate skin wounds. System ic - Low to moderate. Aquatic - Mod!n ste. Detection: The axnmonium and dichromate components must be separately analyzed. See AMMONIA for methods applicable to ainmonjum. See AMMONIUM CHROMATE for methods applicable to dichromate. ------- AMMONIUM FERRICYANIDE (NH 4 ) 3 Fe(CN) 6 Synonym: Amrnonium hexacyanoferrate (III). Description: Red crystalline solid. Sinks and dissolves freely in water. Tends to decompose in strong light, losing ammonia. Toxicity: Human - Low. Aquatic - Low to moderate. Detection: The amrnonlum and ferricyanide components must be separately analyzed. See AMMONIA for methods applicable to ammoniuni. Test for ferricyanide as follows. Acidify sample with 6M 1 - IC L . Then add 1M ferrous sulfate solution. Positive result: deep blue precipitate. (2, 5, 6). ------- AMMONIUM FERROCYANIDE (NH 4 ) 4 Fe(CN) 6 Synonym: Ammon.tum hexacyanoferrate (II ). Description: Yellow to greenish-yellow crystalline solid. Turns blue in air. Sinks and dissolves freely in water 1 Loses ammonia on exposure to air and light. Toxicity: Human - Low. Aquatic - Low to moderate. Detection: The anunonium and ferrocyanide components must be separately analyzed. See AMMONIA for methods applicable to animonium. Test for ferrocyanide as follows. Acidify sample with 6M HCJ. Then add 0. 5M ferric chloride solution. Positive result: deep blue precipitate. (2, 5,6). ------- AMMONZtJM NITRATE NH 4 NO 3 Synonyms: Nitrate of ammonia, Norway saltpeter. Description White, hygroscopic, deliquescent solid. OdorlesS Sinks and dissolves easily. Toxicity: Human - Low. Aquatic - Moderate to low. Other - Promotes growth of algae and plants. Detection: The amrnonlum and nitrate components must be separately analyzed. See AMMONIA for methods applicable to ammonium . Commercial nitrate kits are availabte; sensitivity range i i 0. 3 - 100 ppm. Suppliers include Rich Heflige. Lanttotte, and Taylor. (2,5,6). ------- AMMcflflUM PERCRLORATE NH 4 C1 0 4 Synonyms: AP, APC. Description: White, crystalline solid. Sinks and dissolves freely. A strong oxidizing agent that reacts easily with organic material. Toxicity: Local - Skin irritant. Systemic - (Low.) Aquatic - (Low. } Damaging to plants. Detection; The anunonium and perchiorate components must be separately analyzed. See AMMONIA for methods applicable to ammoniurn. Detect perchiorate as follows. Mix sample with 0. 3% of aqueous methylene blue. Positive result: a violet precipitate that is soluble in hot water. lodides inter- fere 1 but they can be removed beforehand by adding sufficient quantitites of freshly precipitated silver oxide, followed by’ filtering; the filtrate will be free of lodides. (2, 5, 6). ------- AMMONIUM PEROXYDZSULFATE (N 1 1 4 ) 2 S 2 0 8 Synonym: Amrnonium pen ulfate. Description: White, crystalline solid. Sinks and dissolves 1 gradually losing oxygen. Bleaches. Toxicity: Local - (Mild, irritant). Systemic - (Low). Aquatic - (Moderate). Detection: The ammonium and peroxydisulfate components must be separately analyzed. See AMMONIA for methods applicable to ammoniurn. Detect peroxydisulfate as follows. Acid sample to a solution of 2% benzidjne in dilute acetic acid. Positive result: mixture turns blue. Chroniates, perinanganates, and. hypohalites interfere. (1, 5, 6). ------- AMMONIUM PHOSPHATE NH H P0 and (NH) apo 42 4 42 4 Synonyms: Monobasic and dibasic arnn’ionlurn phosphate, primary and secondary ammoniuzn phosphate, Fyrex. Description: Both the mono- and dibasic salts are odorless, white crystalline solids. Both sink and dissolve readily in water, The dibasic salt Is weakly alkaline; the monobasic salt I. weakly acid. In water solution they hydrolyze to ysild aznnionium hydroxide. See AMMONIA. Toxicity: Human - Low. Aquatic - Moderate to low. Other - Promoted growth of algae and plants. Detection; Tb. anunoniurn and phosphate components must be separately analysed. See AMMONIA for methods applicable to ammonlurn. Commercial kits are available for detecting phosphates; sent- tivity range Is 0. 05 - 120 ppm. Suppliers include Hach, Hellige, L.s.motte, and Taylor. (2 5,6). A. good qualitative test for phosphates is to boil a mixture of 2 ml of sample, 2 ml of concentrated ff740 3 , I ml of 7411174031 and 2 ml of ainmonlum molybdate. Positive resulfls a yellow pre- cipitate. For further confirmation, add 1 ml of 0. 5% aqueous hydroqulnone and I ml of 20% sodium sulfite; the mixture wili turn blue if the test Is positIve. (2, 5,6). ------- AMMONTIUM PICRATE CoHz(NOz) 3 0NH 4 Synonyms: Ainmoni urn carhazotate, arninonium plc ronitrate. Description Yellow crystals with sharp, objectionable taste. Sinks and di i solves in water. Very reacüve with inetals Erolosion hazard when dr ,. Toncny: Local - Very irritating; a strong allergen. Systemic - tModerate). Aquade - Moáerate l. Detectior.: The a.mmonittrn and picrate compo nents ntsst be separately analyzed See AMMONIA for methods applicable t arnrnoxuizt. Test for pcrate D v shaking sample with a 1Q ethanol.ic solation of triethvlaxnSne. Positive rescñt picra’ec precipitate. fl, 4’ 1. ------- AMMONIUM SULFATE (NH) SO 4 4 Synonyms: None common. Descriptiont White, crystalline solid. Technical grades are off-white to brownish gray. Sinks and dissolves in water. Water solution is very weakly acid. Toxicity: Human - (Low to none: has been used in medicine and as food additive). Aquatic - Reports vary widely. Probably low to moderate. Detection: The anunonium and sulfate components must be teparately analyzed. See AMMONIA for methods applicable to ammonium. See ALUMINUM SULFATE for detection of sulfate. ------- AMMONIUM SULFIDE NH ITS 4 N. B. True arnmothum su lfide, (NH) 5, is stable only in the absence of moisture and tc&ow 0°C. The arnmonium sulfide of commerce is largely the hydrosulfide (also called the bisulfide). Description: Yellow crystalline solid. Sinks and dis solves readily in water, making a yellow solution whose color grows more intense with aging. The water solution is strongly alkaline. Both the crystals and the solution have the mixed odor of anirnonia (sharp and biting) and hydrogen sulfide (like rotten eggs). Toxicity: Local - Strong irritant. Systemic -(Low). Toxic by skin penetration. A quatic - Moderate. Detection: The amsnoniurn and sulfide components must be separately analysed. See AMMONiA for methods applicable to arnmonium. Detect sulfide by any of the following methods. (I). There are commercially available kit.. for detecting sulfide in water (0. 2 - 20 ppm). Suppliers include HeUige and Larnotte. (2 .5,6) . (U). Acidify the sample with 3M ITC Z to form 14 2 S gas, which may be detected by several cornmer- daily available kits. Suppliers include MSA Scott/Draeger, and Kitagawa. (U I). There is a simple qualitative test for sulfide. Mix sample with GM NH 014 then add 0. SM tetraminezinc nitrate solution. Positive result: white precipitate. (1, 5 .4). ------- AMMONWM THIOCYANATE NH SCN Synonyms: Ammothum rhodanide, ammoni am s ulIocyanide, ainmoniurn sulfocyanate,. Description: Colorless, deiques cent, crystalline solid. Sinks and dissolves freely in water. Toxicity: Human - Slightly toxic by ingestion; may have damaging side effects. Aquatic - Moderate. Detectiom The arnrnoniuxn and thiocyanate components must be separately analyzed. See AMMONIA for methods applicable to ammoniurn. Test for thiocyanate as fo llows. Acidify sample with LM R d 1 then add 0. SM FeCI solution. Positive result: solution turns blood rtd. (Z, 5,6). ------- AMYL ACETATE H 3 CCOOC H 11 N. B. both the n-amyl and isoamyl eaten are corantercially knowu. Synonyms: Amyl acetic ester, banana oil, pear oil, pentacetate, penthanol acetate. Description: Colorless neutral liquid. Pleasant odor rather like bananas or pears. floats on water; very slightly soluble. A layer of vapor wIU tend to accumulate at the water’s surface. Risk of tire or explosion on warm days. ToxicitE Local - Mildly irritating to mucous membranes on exposure to the vapor. System ic - (Low). Muatic - Moderate. Detection: There is no satisfactory method for detecting this substance at water’s edge. Either of the foUowing methods may be used in an improvised laboratory (e. g. a motel roan’ with equipment available). Instrumenta l method of choice: CC with hydrophobic column. The ester can be saponified in about one hour to give ACETIC ACID and PENTANOL. A qualitative test for pentanol is to combine 5 ml of saponification product with S ml of reagent (a 10% solution of ceric axnmonium nitrate ía ZN HNO J. Positive result: solution turns yeflow to red.. 0t12er alcohols interfere. (1,4). ------- ANILINE C 6 H 5 NH Synonyms: A.minobenzene, anriinophen, phenylamine, red oil (a nilxture of aniline and toluidine). Description: Oily liquid; colorless when fresh. Darkens on exposure to air and light. Sinks in water, gradually dissolving. Characteristic sharp odor and burning taste. Can be smelled in concentrations below 1 ppm. Very slightly alkaline. Toxicity: Local - Slight irritant; DANCER: Toxic by skin absorption. Systemic - Highly toxic by ingestion, inhalation, or absorption through intact skin. Aquatic - Moderate. N. B. Soluble aniline derivatives, such as the hydrochloride, have higher aquatic toxicity than aniline. WEAR RESPIRATOR AND PROTECTWE CLOTHING. Detection: Coniniercial liquid and vapor kits for detecting aniline are sensitive to 2 - 10 ppm. Scott/Davis is one supplier. (2,5,6). ------- ANIONIC SURFACTANTS RArSC) 3 Na Includes: A large family of anionic detergents and wetting agents, including the alkyl bensene sulfonate (ABS) detergents 1 many of which are nonbiodegradable. Dozens of brand names, and the principal ingredient of many commercial cleaning agents: ThIs is the largest family of synthetic detergents. Description.: White to pale yellow solid, available as crystals, flakes, powders, and solutions. They sink and dissolve readily, giving a characteristic opalescent soapy solution. Torici ty: Local - May dry and irritate skin; some can cause burns. Systemic - Low.. Aquabc - Reports vary: sometimes High. usually Low. Other- Can cause extensive foaming and sudsing. Bio- degradaMlity varies; Some are very persistent. betection. Shake S ml of sample with 10 inS of chloroform arid 25 ml of methylene blue reagent 150 g Na 2 SO 4 , 6. 8 ml concentrated l4 SO4. and 30 ml of 0. 2% methylene blue solution in I liter of water). Positive result: blue chloroform layer. (1, 4). Commercial test kits are available; liach Chemical Cornpa is one supplier. ------- ANTIMONY POTASSIUM TARTRAT E C 4 H 4 KO 7 Sb Synonyms: Potassium antirnonyl tartrate, tartar emti, tartrated antimony, tartarized antimony. Description: Transparent, whitish, crystalline solid. Sweetish, metallic taste. Sinks and dissolves in water, giving a slightly acid solution. Toxicity: Human - Low to moderate by ingestion. Aquatic - Moderate. N. B. AU soluble antimony compounds are moderately toxic to aquatic life. Detection: The Sb, K, and tartrate components must be separately analyzed. Detect Sb by either of the following methods. (1). Mix sample with 0.02% rhodamine B in 1:10 HC1. Positive result: violet solution or precipitate. (2, 5,6). (II). Acidify sample with 3M HC1, then add a 5% solution of arnmonium sulfide. Positive result: orange precipitate. Z, 5,6). See POTASSIUM CHROMATE for methods applicable to K. To test for tartrates, add add potassium permanganate (IN KMIIO 1 in 5% B,SOL) to sample; carbon dioxide and FORMIC ACID wilIte formed from tartrates. See AMMONIUM CARBONATE for methods applicable to C0 2 ; see FORMIC ACID for its detection method. Many common natural conditions lead to precipitation of antimony compounds from solution. Surface samples of sediment may supply important evidence. Boil these samples in aqua regia. filter, then test the filtrate by either of the methods above. ------- AI4TIMONY TRIC}U 4 ORIDE SbCl 3 Synonyms: An.tirnonous chloride, antimony chloride, butter of antimony, caustic antimony. Descrion Colorless transparent, crystalline solid. Fumes slightly i -n air, Sinks; gradually hydrolyzes to form antimony ozychioride fSbOCl), which settles as a powdery white precipitate. (In salt water, where the chloride ion is prevalent, the oxychioride may not form.) HYDROCHLORIC ACID is formed by hydrolysis of the trichioride. Toxicity: Local - Strongly irritant; corrodes skin. Systemic - Low to moderate by ingestion. Aquatic - Moderate. Other - In addition to the toxic effects Gf the antimony ion. look Sr pH effects due to HYDROCHLORIC ACID. Detection: The Sb and Cl components must be separately analyzed. See ANTIMONY POTASSIUM TARTR.ATE for Sb methods, See AJAMONIUM CHLORIDE for Cl methods. ------- ANTIMONY TRIFLUC)RIDE SbF 3 Synonyms: Antimony fluoride, antirnono us Quo ride. Description: White to gray d.eliquescent crystalline solid. Sinks and dissolves easily in water, readily forming slightly soluble compounds. Toxicity: Local - Very irritating. Systemic - High. Aquatic - Moderate. Look for damage to plants. Detection: The Sb and F components must be separately analyzed. See ANTIMONY POTASSIUM TARTR.ATE for Sb methods. See ALUMINUM FLUORIDE for F methods. ------- ANTIMONY TRIOXIDE Sb 2 03 Synonyms: Antimony white 1 antizmny o xide 1 diantinony trioride, flowers of antimony, Senarinontite Yalentinite, Exitelite, Weisspiessglanz. Description: Odorless, white, crystalline solid. Sinks, dissolving slowly. Toxicity: l iun ian - Low. Aquatic - Moderate. Detectia Only the Sb component need be detected. To detect Sb in solution, see ANTIMONY POTASSIUM TaTRATE. To test sediments and solid. for Sb , flnt di. solve them with 6M HCI, then follow the procedures given (or Sb under ANTIMONY POTASSIUM TART RATE. ------- BAEJUM C I4LOLUDE Ba d 2 Synonyms: None common. Description: White crystalline solid. Very bitter salty taste. Sinks and dissolves readily in water. Water that is rich in COB, sulfate, phosphate, or several other common anions will gradually precipitate barium from solution as a white powder, or make a cloudy white suspension of the precipitate. Toxicity: Human - Moderate by ingestion. Aquatic - Moderate. Toxic to plants and animals. N. B. Soluble barium compounds gradually precipitate from water that is rich in dO 2 , sulfate, phosphate, etc. The white, powdery precipitate may become a milky suspension in turbulent water. Reports on the aquatic toxicity of Ba compounds vary widely: Most are moderately toxic, but reports of very high and rather low toxicity are not unknown. Detection: The Ba and Cl components must be separately analyzed. See AMMONItJM CHLORIDE for methods applicable to Cl. There are several qualitatve methods for detecting Ba; the third method is the most specific, and method (IV) is essential for methodological validity. (I ). lax the sample with a solution of sodium sulfate or sodium carbonate. Positive result: white precipitate. Several metallic ions interfere. (1, 5). (II). Mix the sample with a solution of potassium chrornate. Positive result: heavy yellow precipi- tate. Several metallic ions interfere. (1, 5). (m). Mix 0. 5 ml of sample with 1 ml of cold saturated potassium permanganate and I nil of IN IIZSOa. Immed iately begin adding saturated aqueous solution drop by drop until the purple solution is decolorized. Let stand. Positive result purple precipitate. Only lead interferes. (2, 5). ( IV). To test solid materials for Ba, dissolve the solids in 3M HC1; filter the solution, and discard the undissolved residue. Test the filtrate for Ba by any of the methods above. Because many conditions lead to the precipitation of Ba from solu- tion 1 it is important to assay solids taken from bottom surfaces and suspended solids from suspected waters. ------- BARIUM CYANIDE Ba(CN ) 2 Synonyms: None. Description: White crystalline solid. Decays slowly in air, liberating fumes and vapors of HYDROCYANIC AC , one of the deadliest poisons. Sinks and dissolves freely. Toxicity: Human - Highly toxic by ingestion. DANGER: Vapors of hydrogen cyanide are released from Ba(GN) 2 solutions. Aquatic - Highly toxic; see HYDROCYANIC ACID. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: the Ba and CN components must be separately analysed. See BARIUM CHLORIDE for methods applicable to Ba. Two methods are given for detecting Cr4. Method (I) is very dangerous, because gaseous hydrogen cyanide may be evolved; this gas s a VIOLENT POISON. Use method (i) only if a wdl-circuIated hood is available. Method (II ) is more cumbersome, but it is safe, and does t require elaborate safety precautions. (I). Acidify a very email quantity of sample with HG! to form HYDROCYANEC ACID. Several coinmerciai kits (sensitivity is 0. 05 - 300 pprn are available for detecting FLCN. Suppliers include Hach. Kitagawa, Lamotte, and Scott/Davis. (2, 3, 6). (U). MixO.Smlofsamplewithlmlof2MNaO}i ted I ml of FeSO 4 , then heat to boiling. Let this solution cool. Then acidify with 6M HCJ. Finally, add 0. 5 mi of 0. SM feCl 3 solution. Positive result: deep blue precipitate. (2, 5). ------- BARIUM HYDROXIDE Ba(OH ) 2 Synonyms: Barium hydrate, caustic baryta. Description: Transparent white crystalline solid. Water solubility varies with the degree of hydration in the crystal. Hydrated forms readily absorb carbon dioxide from the air, and are rapidly converted to barium carbonate, which is practically insoluble. The water solution is very alkaline. The hydroxide sinks before dissolving. Toxicity: Human - Varies with the solubility of the hydroxide: insoluble forms are slightly toxic; soluble forms are very toxic. Aquatic - Low to high, depending on solubility. Acidic water leads to increased solubility except where soluble sulfates are present. Detection: Only the Ba component need be analyzed. See BARIUM CHLORIDE for suggested methods. ------- BARIUM NITRATE Synonyms: Hone conm u. Description: Shiny white crystalline solid. Sinks and dissolves freely. Strong oa thzing agent; reacts Md i organic matter. Toxicity: Wbn an - I gb Aqnaflc - Moderate to high. More toxic to plants than to animals. Detection: The Ba and NO 3 components must be analyzed sepa rateLy. Sea BARIUM CHLORIDE for methods applicable to Ba. See AMMONWM NITRATE for methods applicable to NO 3 ------- BENZENE C 6 H 6 Synonyms: Benzol, coal naphtha, coaltar distillate (or light oil or oil), light oil, phene, phenyl hydride, cyclohexatriene. Description: Clear, colorless, refractive, flammable liquid that freezes at 42°F. Industrial grades may be yellowish. Characteristic aromatic odor. Floats on water; very slightly soluble. Toxicity: Local - Mild liquid and vapor irritant. Systemic - PracticaUy nontoxic, but large doses (by ingestion or inhalation) can be fatal. Aquatic - Reports vary widely. High. PROTECTIVE CLOTHING AND RESPIRATOR ADVISABLE. Detection: There are several commercially available kits for detecting benzene as a liquid or a gas. Suppliers include Davis, Kitagawa, MSA, and Scott/Draeger. Sensitivity range is 5-400 ppm. (2, 5,6). Alternatively test for unsaturation by either of the following methods. (I). Test water samples y adding several drops of 1% potassium permanganate. Positive result: the purple permanganate solution is decolorized; bleaching agents and readily oxidizable substances interfere. (1, 3). (II). Where there is a distinct organic phase in the sample, separate this phase and add to it several drops of bromine in carbon tetrachloride (approximately 1%). Positive result: the reddish brown bromine solution is decolorized; readily oxidizable substances interfere. (1, 3). ------- BENZOLC ACID C 6 H 5 COOH Synonyms: Benzenecarbozyb c acid, carboxybenzene, phenyliorxnit acid. Description White crystalline solid. Odor of almond oil. Sinks in water; slightly soluble. Water solutions are acithc. toxicity: Local - Mildly irritating to eyes, mucous membtanes, skin. Systemic - Low. Aquatic - Reports vary widely, from low to high. Other - Look Lot tonc effects in phytoplan]cton. N. B. Metallic salts of beasoic acid (bensoates) are common articles of commerce. Sodium benzoats (bensoate of soda) is one of the most common preservatives used in the food industry; it is more soluble and more toxic than bensoic acid. Detection: Because this acid is not very soluble, pH is of limited utility in presumptive detection. Suspect solid. may be. dissolved in hot alcohol, then tested as follows: this prs sinnptive test may be used for all soluble bensoates. Neutralize the sample with SN NaOR, then mix with 0. SM FeQ 3 solution. Positive result: salmon color. (1 .4,6) , ------- BENZONITRILE C 6 H 5 CN Synonyms: Phenyl cyanide, cyanobenzene. Description: Colorless flammable oil. Odor of almonds; sharp taste. Usually sinks; may float. Slightly soluble. Totcity: Local - Mildly irritating. Systemic - Low to moderate. Aquatic - Moderate. Detection: There is no satisfactory method for detection at watert s edge. in an improvised laboratory (e. g. a motel room, with equipment available), the nitrile could be subjected to vigorous hydrolysis to yield BENZOIC ACT]) and an axnmonium salt. See BENZOIC ACID for suitable detection methods; GC and TJV could also be used in an improvised labora- tory. To detect the amxnoniuxn salt mix with NaOH to render the solution basic, then heat to liberate gaseous AMMONIA. See AMMONIA for suitable detection methods. ------- BENZOYL CHLORIDE C 6 H 5 COC I Synonynt Bezizene carbonyl chloride. Description Transparent, colorless, fuming, pungent liquid. Vapor causes tears. Heavier than water, but de- composes on contacting water into BENZOIC AC ]]) and HYDROCHLORIC ACiD. Tot city: Local - Very irritating to eyes, skin, and mucous membranes. The vapor is a lacrimator; the liquid is corrosive and can cause skin barns. Systemic - Low to moderate: See BENZOIC ACID and HYDROCHLORIC ACID. Aquat ic - Moderate: See BENZOIC ACID and HYDROCHLORIC ACID. Other - Look for corrosion and pH effects. Detection; See BENZOIC ACiD and HYDROCHLORIC ACID for suitable detection methods. ------- BENZYLAM INE C 6 H 5 CH 2 NH 2 Synonyms: Arninotoluene • ma ringine, phenylmethylamine. Description: Colorless to light amber liqtdd. floats; mixes easily with water. Combustible. Strongly alkaline. Toxicity: Local - Very straig irritant. Systemic - (Moderate). Aquatic - Moderate. PROTECTIVE CLOTHING AND RLSPIR&TOR ADVISABLE. Detection: Extract 15 ml of sample with 5 nil of ether. Decant the ether supernatant and add to it 10 ml of 1% ethanolic p-nitrobenzaldehyde solution;(CAUFION: EThER EXTRE*LY FIJ24IABLE.) warmin boiling water for 3 minutes. Then add 2 ml of 2% ajcolwlic KOH. Positive result: solution turns pink or red. (l•5,6). ------- BERYLLiUM SALTS BeCl 2 , Be(N0 3 ) 2 . BeSO 4 etc. Description: Most berylliu m salts are white to faintly yellow, deiques cent, crystalline solids. They sink and dissolve readily, often givin strongly acidic solutions (especially the chloride). Toxicity : Local - Extremely irritating to skin, eyes, and air passage.; often cause contact ulcers, der- inatitis, eye buns. Systemic - High, especiaUy by inhalation. Aquatic - High. Detection: Mix 1 ml of sample with 1 ml of 1 ST. KCN solution and 2 ml of 0. 025% of rnitxwhenyIaaoresorcinol i” 0. IN NaOH. This solution must not be more than 3 days old. Positive result: solution turns pink or red. (1, 5). ------- BORANES BH 3 , (BH 3 )& B H 1 Includes: D*borane decaborane. Descriptioru A series of boron hydrides, ranging from gases to crystals. This series is known up through B 20 H . Several (especially the lower members of the series, such as gaseous diborane) are unstable and react violently with water to form hydrogen and BORIC ACID. Others, such as decaborane , are very slightly soluble crystals that float on water. Toxicity: Local - The lower boranes are irritant. Systemic - See BORIC ACID. Aquatic - See BORIC ACID Detection: The unstable lower boranes react with water to form BORIC ACID. See BORIC ACID for suitable detection methods. The more stable boranes can be hydrolyzed in acid to form BORIC ACID. ------- BORIC ACID H 3 B0 3 Includes the common borates. such as sodium borate (borax), potas S1 urn borotartrats (cream of tartar), aiinmoni am borate 1 calcium boratt, and aluminum borate. Synonyms: Boracic acid. Des cription: Boric acid and the common borates are white crystalline solids. AU but the calcium and a.lurninurn salts are very soluble in water; the calcium and aluminum salts are practically insoluble. The soluble berates may give a fine white precipitate or suspension of calcium borate in hard water, and the precipitate may cause a persistent hazard , particu— larly to plants. Tox icity: Human. Slight. Aquatic - Very slightly toxic to fish; highly toxic to plants. In hard water, soluble berates may give a cloudly suspension or a fine white precipitate which will foul the gills of fish and create a persistent boron hazard to plants. Detection: AU borate. may be tested as follows. (1) Evaporate to dryness 100 ml of sample. (2) To the residue, add methanol in the presence of concentrated sulfuric acid. Positive result: an inflarrirnable vapor that burns with a green flame. (2,4,6). ------- BROM UcE Bra Synonyms: None cornn lon. Description Heavy, dark reddish-brown, fuming, volatile liquid that freezes at 20°F. Vaporizes readily at room temperature. Sinks in water, gradually clis solving. Harsh, penetrating, suffocating odor. Below freezing (31°F), it combines with water to form reddish-brown crystals of hydrated bromine. Powerful oxidizing agent that reacts with organic materials, metals, and other oxidizable substances. Toxicity: Local - Vapor is highly irritating liquid causes severe burns. Systemic - Highly corrosive and toxic by inhalation and ingestion. Aquatic - Highly toxic to all forms of aquatic life. WEAR RESPIRATOR AND PROTECT1VE CLOTHING. Detection: There are several commercially available kits for detecting bromine as a liquid or a gas ; sensitivity range is 0. 01 — 300 ppm. Suppliers include HeUige, Kitagawa, Lamotte, MSA, Scott/Davis, and Taylor. (2,5,6). ------- BUTYLACETATE HCCOOC 3 4 Includes: All forms of butyb n, see, tert , and iso. Synonyms: Acetic acid butyl ester; butyl ethanoate. Descñption Clear, colorless, flammable, liquid. Pleasant, fruity odor. floats; very slightly soluble. Vapor accumulates at the waterts surface. Toxicity: Local - Vapor irritating, especially to eyes. Systemic - Low, but high concentrations are narcotic, Aquatic - Low to moderate. Detection: There is no satisfactory method for detecting at water’s edge. In art improvised laboratory use UC ‘with hydrophobic column or proceed as follows. Saponify ester (about one hour) to yield ACETIC ACID and BUTYL ALCOHOL; see these entries for suitable detection methods. ------- BUTYL ACRYLATE H 2 C:GHCOQC 4 H 9 Synonym: Acrylic acid a- butyl ester. Description: Colorless liquid. Sharp, fragrant odor. Floats on water, and is nearly insoluble. Combustible. Polymerizes readily upon heating unless stabilized (often with bydroquinone monomethyl). Tot city: Acute - Vapor and liquid are mildly irritating. Systemic - Low. Aquatic - (Low). Detection: There is no satisfactory method for detection at waterts edge. As a gross presumptive test, the following method for identifying unsaturation is recommended. Separate the supernatant organic phase if possible. Add to it several drops of bromine in carbon tetrachjoride (about 1% solu- tion). Positive result: the bromine color disappears. (1, 3, 6). In an improvised laboratory, hydrolyze the ester to free the ACRYLIC ACID, then detect ACRYLIC ACID by GC or wet-chemical means. ------- BUTYL ALCOHOL C 4 H 9 OH Includes: All conxrnon butyl alcohols: n, sec tert, and iso. Synonyirn ButanoL Description: AU but the tert form are colorless liquids with a pleasant fruity odor (reminiscent of grapes); they float on water, dissolving gradually. The tat alcohol is a crystalline solid that smells like camphor; it floats on water, and dissolves. Toxicity: Local - Irritant vapor that can cause eye burns. Systemic - Low. A quat - Low to moderate. Detection: Test for aliphatic alcohol as follows. Combine Z ml of sample with 5 ml of reagent (a 10% solution of ceric ammonium nitrate in ZN nitric acid). Positive result: solution turns yellow to red. A U aliphatic alcohols (prim-, sec-. and tort-) give positive result. (1 .4,6). ------- BUTYLAMINE C 4 H 9 NH 2 Includes: n, see, tert , and iso isomers. Synonym: Aminobutane. Description; All are colorless, volatile liquids that smell of ammonia. All but the sec isomer are readily miscible with water; the sec form dissolves gradually. All are flammable. Toxicity: Local - All but the iso form are slightly irritating; the iso form can cause blistering of the skin. Systemic - Low. Aquatic - Moderate. Detection: There are commercial kits for detecting butylansine as a liquid or gas. One supplier is MSA; sensitivity range of MSA kit is 2-100 ppm. (1 or 2; 4 or 5; 6). ------- BUTYLENE GLYCOL C 4 11 10 0 2 Synonyms: Butanediol, dihydroxybutane. Includes: The three common structural isomers: 1,3; 1,4; and 2,3, Description. All isomers are practically colorless and odorless, and nearLy the same weight as water (they may sink or float, depending on dissolved solids in the water). The 1,3 and 1,4 isomers are viscous hygroecopic liquids; the 2, 3 isomer is also a heavy liquid in sumnmer heat, but at room temperature it is crystalline: it usually floats, and readily dissolves. Toxicity: Human - Low. Aquatic - Low. Other - A major SOD problem. Look for SOD effects. Detection: There is no suitable method for detection at waters edge. In an improvised laboratory, use GC with hydrophobic column for detection. ------- BTJTYL MERCAPTAN C 4 H 9 SR Includes the four con-smon structural isomers: n, sec, text, and iso . Synonyrn Butanethiol. Description: All are colorless, mobile liquids with an over- powering, obnoxious odor like that of skunks. All float on water, and are slightly soluble. Very flammable. Toxicity: Human - Revolting odor may cause nausea. Narcotic in high concentrations. Aquatic - (Low). Other - Butyl mercaptan is one of the foulest-smelling substances known; taste and odor problems will affect the water as long as it is present. RESPiRATOR ADVISABLE. Detection: The offensive odor of this compound can be sensed by the unaided nose of the investigator in subtotc con- centrations. (1, 5, 6). If desired, test for SR group as follows; all primary and secondary thiols give a ?ositive response, and water that is rich in dissolved sumdes may also give a positive response. in a test tube, mix I ml of sample with Z nil concentrated NH 4 OH. Immediately cover with lead acetate paper and place the tube in a boiling-water bath. Positive result: black stain on the lead acetate paper. (1,4, 6). ------- CADMIUM CHLORIDE CdC1 2 Synonyms: None common- Descnpbon Hygroscopic. white crysta lline solid. Odorless. Sinks and dissolves freely. Toxicity : Rtnrian - High. Aquatic - High to moderate (threshold varies from 0.1W 72). N. 8. All soluble cadmium compounds are highly toxic to most forms of life. Detection: The Cd and Cl components must be separately analyzed. See AMMONiIJM CHLORIDE for methods applicable to CL . (I). To detect Cd. mix I ml of sample with 1 ml of 10% NaOH and I ml of KCN solution. Then add 1 ml of 0.1% alcoholic d.i p-nitropheny1carbazide solution and 2 in] of 40% formaldehyde. Positive result: blue-green solution or precipitate. (2,6). (II). A less specific test has the advantage of simplicity. Mix sample with a concentrated solution of H 2 S. Positive result: bright yellow or orange precipi- tate. Unclear result: precipitate of any color. Negative result: no precipitate. (1. 4). (ill). Cd compounds may precipitate from solution under the action of dissolved CO 2 . soluble sulfides, etc. Collect surface sediment samples, boil th in aqua regia. then test the solution by method (I). ------- CADMIUM NITRATE Cd(NO 3 )z Synonyms: None common. Description: White solid, amorphous or crystalline. liygroscopic. Sinks and dissolves freely. Danger of fire and explosion in contact with organic material. Toxicity: Human - High. Aquatic - High. Detection: The Cd and NO 3 components must be separately analyzed. See CADMIUM CHLORIDE for Cd methods. See AMMONIUM NITRATE for NO 3 methods. ------- CADMIUM SULFATE CdSO 4 Synonyms: None common. Descriptiorn Odorless, white, crystnlHne solid. Sinks and dissolves freely in water 0 Toxicity: Human - High. Aquatic - High. Detection: The Cd and SO 4 components mast be separately analyzed. See CADMIUM CHLORIDE for Cd methods. See ALUMINUM SULFATE for SO 4 thethods. ------- CALCIUM CARBIDE CaC 2 Synonyms: Acetylenogen, carbide. Description: Grayish-black solid (lumps or crystals). Sinks in water, but is rapidly decomposed to ACETYLENE gas and lime (calcium hydroxide). Toxicity: Low. See ACETYLENE. Detection: ACETYLENE and lime, the reaction products of CaC 2 and water, must be separately analyzed. See ACETYLENE for suitable detection methods. Lime precipitates from solution. Coflect surface sediment samples and mix them with 3M HC1 to redlissolve the Ca. Check water samples for high Ca values too. Ca is so prevalent and so widely distributed, Ca detection is of limited value. A gross qualitative test for Ca is given for completeness’ sake; Ba and Sr interfere. Mix 1 nil of sample with 4 ml of 1% ethanolic bis(Z-hydroxyanil)glyoxal. Add I ml of 10% NaCN and 10% NaOH solution; mix well. Add 2 nil of chloroform. Positive retult: chloroform layer turns red. (1,5,6). ------- AL IUM CYANIDE Ca{CN) 1 Synonyms: None comn n. Description: White. crystalline solid. Decomposes in moist air and in water to HYDROCYANIC ACID, one of the most poisonous substances known. Sinks and dissolves readily in water, but is decomposed to HYDROCYANIC ACiD; acidic water liberates HYDROCYANIC ACID more rapidly than neutral or basic water. Toricity: thgbly toxic to man and aquatic life: See HYDRO- CYANIC ACID. WL&R RESPIRATOR AND PROTECTIVE CLOTHING. Detection: It is the CN component that is important. See BARIUM CYANIDE for CN detection methods. See CALCIUM CARBIDE for Ca detection method and comment. ------- CALCIUM HYPOCHLORITE Ca(OCl) 2 Synonyms: Calcium oxychioride, Losanfin; ingredient of Caporit, HTH, and Perchloron. Des cription: White, crystaUlne solid. Smells like chlorine bleach. Sinks; slightly soluble in water. A strong bleaching and otdizing agent. Hydrolyzes in water to liberate free chlorine. Tot city: Local - Low; irritating and corrosive in high concentrations, Systemic -(Low). Aquatic - Extremely toxic to phytoplankton, especially blue-green algae. Toxicity to higher forms of aquatic life probably slight. Other - Look for bleaching and for corrosion effects. Detection: This hypochiorite bydrclyzes to liberate free chlorine in water; see CkILORINE for detection methods. The hypochiorite ion may also be used for detection; see HYPOCHLOROUS ACID for method. ------- CALCIUM P}K PWDE Ca 3 P 2 Synonyaxc P ophor. Descriplion Red-brown crystals or gray granular masses. Heater than water, but decomposed by it to liberate pàosphine a spontaneously flammable and extremely toxic gas that smells of decaying flab and is slightly soluble in water. Toxicity: Local - Irritates the lungs and air passages. Systemic - High, especially by inhalation. Aqua t ic - Probably highly toxic to any animal in contact with the phosphine. Damage is likely to be tocalised since phosphine is * slightly soluble g a WEAR RESPIRATOL Detection: Based on detection of phosphine; several commercial kits are available (reading range is 0.. 1 - SQ pprn . Suppliers include Ritagara MSA and Scott/Davis (2, 5, 6). ------- CARBON DJSTJLFIDE cs 2 Synonym: Carbon his ulfide. Descripfion Clear, colorless or faintly yellow, extr ely fisable liquicL Reagent grades are almost odorless, but commercial grades have a strong, disagreeable smell that is detectable in great dilution. Sinks in water; very slightly soluble. The vapors are ex- plosive. Toxicitr Acute - Low. Systemic - Moderate by inha lation; low by ingestion or skin absorption. Aquatic - Moderate, (especially tone to bottom life). Detectioxu Commercial kits for detecting the liquid or the vapor of CS ; snsitivity range is 5-500 pjxn. Suppliers incluje Kitagawa, MSA. aM Scott/Davis. (2, 5 ,6). ------- CARBON MONOXIDE Co Synonyms 2 None common. Description: Colorless, practically tasteless and odorless gas or liquefied gas. The liquefied gas floats on water, but rapidly evaporates. Very slightly soluble in water (Z4 mg/liter). flammable: Barns with violet or bright blue flame. Toxicity: Local . None. Systemic - Highly toxic by inhalation. Aquatic - High. WEAR RE PlRATOR WHEREVER CONCENTRAT IO 7C ABOVE A FEW p t ARE EXPECTED. D.tection There are servera.1 commercial kits; sensitivity range is 10-3000 pç*n. Suppliers include Kitagawa, IIIISA, and Scott/Davis. (2,5 .6). ------- CARBON TETRACHLORIDE C d 4 Synonyms: Bensinoform, carbon chloride 1 perchioromethane, tetrachlorornethane. Descrion Colorless volatile liquid that smells like cleaning fluid.. It yields vapors that are much heater than air, and tend. to collect at the water’s surface. Sinks; practically insoluble. Does not burn. Toxicity: Local - May dry, crack, and irritate skin. System ic - Very slightly tonc by all routes. 1000 to 2000 ppm in air ii lethal for man. Aquatic - Probably low; especially toxic to bottom life. Detection: There are commercial kits for both the liquid and the gas; sensitivity range is 10- 300 ppm. Suppliers include Kitagawa, MSA, and Scott/Davis. (2, SF6). ------- CIfiAMUC ACID HC IO 3 Synonyms: None common. Descriptionz Colorless soiction; completely miscible with water. Very powerful oxidizing agent. Decomposes at 40°C. Toxicity: Local - Very irritating and corrosive. Systemic - {Probably low). Inha lation hazard. Muatic - Very corrosive in high concentrations to all organic matter. Chioric acid and chiorates are widely used as herbicides and defoliants. Look for damage to plant life. Highly toxic to phytoplankton. RESPIRATOR AND PROTECTiVE CLOTHING ADVISABLE. Detec t ion (I). Use pH indicator paper or p11 meter to check for strong acid. (1,3). (11). Test for C1O,% ion as follows. Add 10 m l of ice- cold 9M 112504 to S rail of sample. Add 0.5 ml of 5% brucine in glacial acetic acid. Positive result: solution turn blue. Periodates and nitrate. interfere. (l 5). (Ill). Alternatively, test for C10 3 by adding 0. 5 ml of saturated aqueous MnS0 4 aM 0. 5 ml of syrupy ff90 3 to 1 ml of sample. Heat and cooL Positive result: solution turns violet. Bromates iodates pe.rfodatea, and nitrates interfere. (1, 5). ------- CHLORINE ci Synonyms: None common. Description2 Gas or compressed, liquefied gas. Gas is greenish- yellow and much heavier than air. The liquid is clear amber. Sharp, biting odor, detect- able in great dilution. Sinks in water; slightly soluble (about 1%). The water solution is acidic. Toxicity: Local - Powerful blistering agent and respiratory irritant; irritates skin. Systemic - Corrodes organic matter; very harmful to lungs and respiratory passages. Aquatic - Very corrosive in high concentrations. Highly toxic to phytoplankton, especially algae, and to fish. Damage is likely to be especially severe to bottom life. Dilute solutions may be very toxic to plants. RESPIRATOR AND PROTECTIVE CLOTHING ADVISABLE. Detection: There are commercial kits for detecting chlorine; sensitivity range is 0. 02 - 30 ppm. Suppliers include Hach, HeUige, Kitagawa, Lamotte, Scott/Davis, and Taylor. (2,4,6). ------- CHLOROACETIC ACID H 2 CC1COOH Synonyms: Monochioroac etic acid; MCA. Descriptiont Deliquescent colorless to pale brown crystalline solid Sinks and dissolves readily. Totcity Local - Irritating and corrosive. Systemic - Moderate. Aquatic - (Moderate). Look for corrosio n effects. This acid is a known herbicide; look for damage to plant life. PROTECTWE CLOTHING ADVISABLE. Detection: Acidify samples with MC i, then follow presumptive detection method given for ACETIC ACID. ------- CRWROAMINES NH 2 C1, NIiCI 2 , Nd 3 , and AkArSO 2 NNaCl pcIudes both inorganic and organic chloraniines. Sywnyms: Chlorantines; Z of the most common organic chloramines are chioranilnes B and T. Description: The inorganic cblora.rnine.s arc colorless 1 unstable, pungent liquids that are very soluble in water, where they slowly decompose form nitrogen gas, HYDRO- CHLORIC ACID, and AMMONIUM CHLORIDE. The organic chlorarnines are white to off-whit, crystalline solids that smell of chlorine and die solve fairly well in water. Cbloraxnine-3 tuna litmus blue, then bleaches it. The organic chlorarnines are used as topical antiseptics. Tc icity : Local - The inorganic a are much more irritating than the organic.. Systemic - (Moderate). Aquatic - The inorganic. are probably highly toxic; the organic. are probably moderately totc. Detection: There are separate detection methods for the organic and inorganic chloroaxnine.. Inorganic chloroantines are detected through their hydrolytic products. See H? DROCHLORIC ACID and AMMONIUM CHLORIDE for methods. For organic chloroatnines, mix the sample with concentrated H 2 SO 4 , dilute with water, then test for A.MMON1UM CHLORIDE. ------- CHLOROBENZENE C 6 1 1 5 C1 Synonyms: Chlorobenzol, phenyl chloride. Des c riptiorn Clear, co mobile, volatile, flammable liquid that smells like almonds. Sinks in water; practically insoluble. T otcity: Local - Liquid is slightly irritating. Systemic - Low; high concentrations are narcotic. Aquatic - Moderate. Detection: There are commercial kits for detecting chiorobensene; sensitivity range is JO-ZOO ppm. One supplier is MSA. Kits are available for both the Liquid and the gas. (Z 5 6). ------- tULOROBUTADIENE }i 2 C:CHCCI:CH 2 Sysonyrn: Chloroprene. Description: Colorless, flammable, and explosive liquid. Floats on water; slightly soluble. Taicity: Local - lrritant to eyes, akin, mucous membranes. Systemic - Moderate to high, especially by inhalation. Aquatic - (Low to moderate). USPIRATOR AND PROTECTIVE CWTHIM3 ADVISABLE. t*Iection: Test as butadiene. Mix 2 ml of sample with. 2 m l of methanol and 2 ml of 1% mercuric acetate solution. Positive result: highly colored addition compound. Butadiene interferes. (1, 4.6). Test for halogeuation as follows. To I ml of sample add S ml of freshly prepared 15% Na! in acetone (DO NOT USE IF THE IODIDE SOLUTION HAS TURNED REDDISH BROWN). Positive result: a reddish-brown precipitate. If the result is unclear, put test solution in hot water (about 120°F) for 5-10 minutes; if no precipitate forms, the test is negative. All halogenated organacs interfere. (1, 3, 6). ------- CRC 1 3 Synonyms: Methyl trichic ride, trichloromethane; improperly , Iorrnyl chloride or tricbloride. Descriptiore Clear, colorless, highly refractive, volatile liquid. Characteristic sweetish odor. Burning, sweet taste. Sinks in water; slightly soluble. Decomposed by beat and light. Toxicity: Local - Irritating vapor aM liquid. Systemic - Low to moderate; narcotic in high concentra t ion. Aquatic - Moderate. Detection: There are commercial kits for chk,roform; sensitivity range is Z5-600 p n. Both liquid and vapor may be detected. Suppliers include Kitagawa. MSA. and Scott/Davis. (Z 5,6). ------- CELOROPLATINIC ACm H 2 PtCI 6 Synony!n Platinic chloride. oescriptionz Red-brown crystals that sink and dissolve in water. Ttcity: Human — Moderate. Aquatic - Moderate. Dd.ction Check areas of suspected high concentration with pH indicator or meter for acidity. (1. 3). For more specific test, mix 5 ml of sample with 10 nil of 5% aniline in 10% HCL A precipitate forms if chioroplatinic acid is present. Collect the precipitate and add it to ethanol containing a small amount of HC 1; then heat in boiling water. Positive result: the precipitate redissolves. (l 4,6). ------- CHLOROSULFON IC Acm CLSO 2 OH Synonym: Sulfuric cbiorohydrin. Description: Clear to cloudy, colorless to pale yeflow, fuming very corrosive liquid. Decomposed by water to HYDROCHLORIC ACID and SULFURIC ACID. To xicity: Local - Very corrosive and irritating. Systemic and Aquatic - See HYDROCHLORIC ACID and SUI 4 FURZC ACID. Toxicity varies with p 1 1 . Other - Look for corrosion damage. Detection: Detect as HYDROCHLORIC ACID and SULFURIC ACID See these entries for suggested methods. ------- CBWROTR IAZIDE C 7 H 6 C1I’J 30452 (two condensed rings) Synonyms: There are many pharmaceutical synonyms for this compound, its hydrated form, and its sodium salt. Description White crystalline solid. The sodium salt is presumably soluble in water: the other forms are practically insoluble. These compounds are widely used as diuretics and antihypertensives. Toxicity: Local - Probably none. Systemic - Low. Aquatic - (Low).. Ddection: Detection may be based in any of several presumptive tests: pnmary amine (see PROPYLAMINE), secondary amine (see BENZYLAMINE and AM1NC)ETHYL ETHANOL AMINE I. *nd nnsathrabon (see I1ENZENE and AB IETIC ACID). Specific identification may be accomplished in an improvised laboratory equipped with a 1W spectro- photometer. ------- CHLOROUS ACID 1 1C102 Synonyms: None common. Descriptiorn Clear, colorless, liquid, completely miscible with water. Strong oxidizing agent. Concentrated solutions are unstable, and release C10 2 . Toxicity : Local - High concentrations are corrosive and irritating. Systemic - (Low). Aquatic - Very toxic to plants aM phytoplankton; low toxicity for animals. Other - Look for corrosion damage. Detection: Commercial detectors are available; sensitivity range is 0. 1-500 ppm. Suppliers include Kitagawa , MSA, and Scott/Data. (1 or 2,5,6). ------- CITRIC ACID CH 2 COOHC(OH)COCJHCH 2 COOH Synonyms: Hydroxypropanetricarboxylic acid, hydroxycarballylic acid. Description: White, crystalline solid. Odorless. Strong sour taste. Sinks in water; very soluble. The common citrates (sodium, magnesium, potassium) are soluble white crystals or powders. Toxicity: Local - Mild irritant Systemic - Low. Aquatic - Low. Other - Increases nOD. Detection: Mix 1 ml of sample with 1 ml of 0. O IM KMnO 4 and 1 ml of saturated bromine water; warm slightly. Then add solid sulfosalicylic acid until the color of bromine disappears. Positive result: white precipitate. (1, 56). ------- COBALT CHLORIDE CoC1 2 Synonym: Cobaltous chloride. Description Pale blue hygroscopic leaflets or pink to red slightly deliquescent crystals. Sinks and dissolves in water, giving a pink solution that turns blue in response to acids or heating. Aqueous solutions are acidic. Toxicity: Local - Low. (Used to treat anemias). Aquatic - High. N. B. All soluble cobalt compounds are highly or moderately toxic to a wide variety of aquatic life, including eaprophytic bacteria and fish. Detection? Cobalt can be precipitated from solution by aeveral common natural processes; he certain to analyite surface samples of sediment Boil the solids in aqua regia to redissolve the Co. then proceed (as below) for soluble Co. The Co and Cl components must be analyzed separately. See AMMONIUM CHLORIDE for methods suitable for C l. To detect Co mix I ml of sample with 1 ml of reagent (made from 1 g of 1-nitroso- Z-naphthol and SO ml of glacial acetic acid in 1 liter of water). Positive result: brown stain. Ferric ion interferes. (l 4). ------- COBALT NITRATE CO(NO 3 )z Synonynt Cobaltous nitrate. Descriptiorn Deliquescent, red, crystafline solid. Sinks and dissolves readily in water. Good oxidizing agent; fire risk in contact with organic material. Toxicity: Human - Low to moderate. Aquatic - Moderate to high. Detection: The Co and NO 3 components must be separately analyzed. See COBALT CHLORIDE for Co methods. See AMMONIUM NITRATE for NO 3 methods. ------- COBALT SULFATE Co50 4 Synonym: Cobaitous sulfate. Description Red to lavender crystalline solid; deliquescent in moist air. Sinks and dissolves freely in water. Toxicity: Human - (Low). Aquatic - Moderate to high. Detection: The Co and SO 4 components must be separately analysed. See COBALT CHLORIDE for Co methods. See AMMONIUM SULFATE for SO 4 methods. ------- COPPER CHLORIDE CuC I 2 Synonyrm Cupric chloride. Descriptioxu Blue- green crystalline solid. Deliquescent in moist air; efflorescent in dry air. Sinks in water; dissolves readily. The aqueous solution is acidic. Toxicity: Local - Irritant. Systemic - (Low). Aquatic - High. H. B. AU soluble copper compounds are highly toxic to a wide variety of aquatic life; even in subtoxic concentrations, it can turn shellfish green, thereby destroying their commercial value. Copper com- pounds characteristically give intense blue or blue-green solutions. Detection: The Cu and Cl components must be analyzed separately. See AMMONIUM CHLORIDE for Cl methods. Co mmercial kits are available for testing Cu in solution; sensitivity range is 0-3 pjn Suppliers include Lamotte, Taylor, Hel.lige, and Hatth. (2, 5,6). There are several simple qualitative tests. (I). Addition of HH 4 OH to dissolved copper gives a dark blue solution (Z, 5). (U). Mix 1 ml of sample with I nil of 20% rnalonic acid and I ml of saturated rubeanic acid in methanoL Positive result: solution turns greenish black. Silver interferes. (1, 5,6). ------- COPPER NITRATE Cu(N0 3 ) 2 Synonym: Cupric nitrate. Description: Deliquescent, blue, crystalline solid. Sinks and dissolves freely in water. A good oxidizing material that may combust or explode violently in contact with organic materials. Used as an insecticide in agriculture. The aqueous solution is acidic. Toxicity: Local - Irritant; stains skin. Systemic - (Low). Aquatic - High. Look for damage to fish and insect populations. Other - May promote the growth of algae and plants. Detectiorn The Cu and NO 3 components must be separately analyzed. See COPPER CHLORIDE for Cu methods. See AMMONTTJM NITRATE for NO 3 methods. ------- COPPER SULFATE CuSO 4 Synonyms: Blue copperas, blue stone, blue vitriol, cupric sulfate. Description: Blue crystalline solid that effloreces in dry air. Sinks and dis solves readily in water. Nauseous metallic taste. Toxicity: Local - Irritant. Systemic - Moderate by ingestion; low by skin absorption. Aquatic - High to moderate. Detection: The Cu and SO 4 components must be separately analyzed. See COPPER CHLORiDE for Cu methods. See ALUMINUM SULFATE for SO 4 methods. ------- CRESOL UOC 6 R 4 CH 3 Includes: the ineta, ortho , and para isomers. Synonyms: Cresylic acid, rnethylphenol, hydroxytoluene. Description; Clear liquid or crystalline solid that turns brown with age and exposure- Sinks; slightly soluble. May not sink all the way to bottom in salt water. Smells and tastes like Lysol and similar disinfectants. Toxicity: Local - Strongly irritant; may burn skin. Systemic - Low to ntderate; rasdly absorbed through the skin. Aquatic - High to moderate. WEAR PROTECTIVE CLOTIUNG. Detection : (1). A simple qualitative tnt for aromatic alcohols is as follows. Mix 2 ml of sample with S ml of reagent (a 10% solution of cenc anirnonium nitrate in ZN )V40 3 ). Positive result: brawn to greenish-brown precipitate. Jill low-molecular-weight aromatic alcohols test positive. 0,4). (U). A simple qualitative test for p-cresol is as follows. Mix 2 ml of sample with 2 ml of ethanol aM 2 ml of concentrated 10103. Add I ml of 0.1% alpba-nitroso- beta..napIttbol in ethanink Positive result: solution turns red. Some other phenols inter- fere. (1, 5,6). (U I). The ortho and mets isomers can be detected by mIxIng the sample with 2, 6-dibromoquinone in buffered solution. Positive result: solution turns red.. Other phenolic compounds inter- fere. fl,4,6). ------- GROTONALDEHYDE H 3 CCItCHCHO Sponyms: Butenal, crotonic aidebyde; znethylacrolein. Description: Clear, colorless, mobile, flaxnniable liquid. Turns pale yellow on contact ‘ w ith air and light. S harp, suffocating odor, floats on water; slightly soluble. TScltr Local - Strong lacriniatar; highly irritating to eyes. mucous membranes, and skin; both vapor and liquid are extremely irritating. Liquid can cause severe burns Systemic - Moderate to high by all routes, including absorption through intact skin. Aquatic - (Moderate). WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Ditection Mix S ml of sample with 2 ml of 1% zn-phenylencdiamine hydrochloride and 1% oxalic acid in ethanol. Warm in a hot -water bath for 5 minutes. Positive result: solution turns purple. (1, 5, 6). ------- CYANAMIDE HN:C:NH or N:. CNH 2 Synonyms: Hydrogen cyanarnide, carbamic nitrile, cyanogenarnide, carbodiimide. Description: White, crystalline, deliquescent solid. Sinks and dis solves freely in water. Combustible. Neutral aqueous solutions are not stable, particularly if the solution comes into contact with metals. Totcity: Local - Very irritating and caustic, particularly to moist skin. Systemic - Moderate by ingestion or inhalation. Aquatic - (Moderate). N. B. Cyanarnide totcity does not involve the cyanide effect. WEAR PROTECTIVE CLOTHiNG: RESPIRATOR ADVISABLE IN VICINITY OF RAPIDS AND FALLS. Detection: This detection requires 2 separate steps. (1) Test sample for HYDROCYANIC ACID (use any of the methods given at that entry). Ft the test for HCI4 is negative, proceed to step 2. (2) Place 1 ml of sample in a test tube; add 0. 1 g of zinc (preferably strips) and a few drops of 20% HCI. Test again for HCN. If step 1 is negative and step 2 is positive for HCN, the sample is presumptively positive for CYANAMIDE. Other nitriles may interfere. (1 5,6). ------- CYANOACETIC AC iD CNCH 2 COOH Sponyrn: Malonic nitrile. Description: Hygroscopic, white crystalline solid that sinks and dissolves in water. Tstcity: Human - High. Aquatic - (High). PROTZCTWE CLOTHING ADVISABLE. Detection: There is no suitable method for use at water’s edge. in an improvised laboratory, esterify the sample, extract it, then use GC for detection. (2, 3.6). ------- CYANOBTJTADIENE N:. CCthCHCThCHZ Synonyms: Pentanedieneonitrile • cyanoprene, vinylac rylonitrile. Description (Colorless) liquid that floats (very slightly soluble). Polymerises into synthetic rubber. Toxicity: Human and aquatic - Moderate. Detection There is no simple specific test for this substance. As a gross presumptive test, use the method given for CHLOROB UTADIENE. ------- CTM4OGEN BROMIDE BrCN Sy nym: Bromine cyanide. Description: Colorless crystalline solid; volatile at ordinary temperatures. Sinks and dissolves in water. Aqueous solutions, especially if alkaline, are unstable. tazicity: Local - Llighly irritant and toxic vapors. Systemic - Same as HYDROCYANIC ACID: High. Aquatic - Sante as HYDROCYANIC ACiD: High. TEAR RESPIRATOR AND PROTECTIVE CLOTHiNG. DdectIon: Mix sample with a 10% solution of o-toluidine in pyridine. Positive result: solution turns violet or red. (1, 4). Since cyanogen bromide is unstable in water, also test for the hydrolysis products; see detection methods for HYDROCYANIC ACID and bromide (see entry at ACETYL BROMIDE). ------- CYANOGEN CHLORIDE CNC1 Synonym: Chlorine cyanide. Description: Colorless liquid or gas (b . p. is 57°F) which sinks and die solves in water. Toxicity: Local - Highly toxic and irritant vapors. Systemic - High. See HYDROCYANIC ACID. Aquatic - High. See HYDROCYANIC ACID. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: See CYANOGEN BROMIDE and A.MMONIUM CHLORIDE. ------- CYCLOHEXANE Synonyms: Hexahydrobenz ene, hexamethylene, he.xanaphthene. Description: Colorless, mobile, extremely flammable liquid. Mild, sweet odor. Floats on water practically insoluble. to city: Human - Low. Aquatic - Reports vary from moderate to low. petection: Commercial kits are available: sensitivity range is 10 -600 ppm. One supplier is Ritagawa. (1,4, 6j. ------- DIAMINOETHANE 8 2 N(Cfl 2 ) 1 NH 2 Synonyms: Ethyl enedianiine, ethanodiamine. Descriptiont Volatile, colorless liquid that readily absorbs CO 1 from the air, flammable. Mild anrnoniacal odor. Sinks and dissolves readily. Strongly basic. Toxicity Local - Very irritating as liquid and vapor. May burn tissues. Systemic - Moderately toxic by all routes. Aquatic. Moderate to bigL WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Use gross presumptive test for primary amirtes. See PROPYLAMINE for recommended methods. ------- DIAMY LAMINE (C 5 H 11 ) 1 N}{ Synonym: Dipentylarnine. Description: Clear, colorless liquid. Floats; very slightly soluble. Toxicity; Human - (Unknown; may be moderate). Aquatic - High to moderate. Detection: Use either presumptive test for secondary arnines, as follows. ( I ). Mix 2 ml of sample with S ml of 0. 1M beuzenesulfonyl chloride in 10% aqueous NaOH. Positive result: immediate for- mation of a crystalline precipitate. (1, 3). (11). Prepare reagent by dissolving 0. 5 g NiCl 2 hexahydrate in 100 ml of water. While shaking, add CS 1 to slight excess. Just before testing sample, add 2 ml of con- centrated NH 4 0H to S ml of reagent. Then add 2 nil of sample. Positive result: a well-defined precipitate. (1, 3). ------- DIBUTYL Pl’ITI-IALATE C 4 H 9 00C},C 6 H 4 Synonyms: Butyl phthalate, DBP, phthalic acid dibutyl ester. Description: Colorless tdories s, nonvola le , stable, oily liquid. Sinks in fresh water (but may float on salt water i; very slightly soluble. Toxicity: Local - Somewhat irritating. Systemic - Low Lq uati - High; tish are especially sensitive . Detection: The only wet-chemical test that can be easily used 3t water s edge is a gross presumptive test for unsaturation. Use either of the following methods. iP . Test water samples by adding several drops of ITo potassium permanganate. Pcsitive result: the purple perrnanganate solution is decolorized. (1, 3). ll). Where there is a distinct organic phase in the sample, separate this phase and add to it several drops cf bromine in carbon tetrachioride (approximately 1%). Positive result: the reddish-brown bromine solution is decolorized. (1, 3). ------- DICHLORCBENZENE C 1 H 4 Cl 2 Includes all three structural isomers: meta, ortho , and para . Description: All three isomers are heavier than water and practically insoluble. Meta is a colorless liquid. Ortho is a clear 1 volatile, stabler heavy liquid with a pleasant, aromatic odor similar to some dry—cleaning fluids. The para isomer is best known for its frequent use in mothballs and moth- flakes. It is a volatile 1 whit& crystalline solid that sublimes without leaving a residue. Character- istic mothball odor. Toxicity: Local - The ortho isomer is highly irritating; otherwise, slight. Systemic - Low. Aquatic - Moderate; probably especially harmful to insects. Detection: There are commercial kits for detection; sensitivity range is 10-200 ppm. Suppliers include MSA and Scott/Davis. (1 or 2,5,6). ------- DICHLOROETHANE (1) C1 2 HCCH 3 and (2) CLH 2 CCH 2 C1 Synonyms: Formula (1) is ethylidene chloride; formula (2) is ethylene thchloflde, ethylene chloride, and Dutch oil. Descripbon Both forms are flanunable, colorless, neutral, mobile liquids, with a characteristic sweet odor Like that of ether or chloroform, and a sweet taste. Both forms sink in water, and are very slightly soluble. Toricity: Local . Irritant; formula (2) i i strongly irritant. Systemic - Moderate. Aquatic - Moderate to low. RESPIRATOk AND PROTECTW E CLOTHING ADVISABLE. Detection: Commercial detection kits are available; sensitivity range is 25 -500 ppm. Suppliers include MSA and Scott/Dtvis. (l,5,6 . ------- DICHLOROMETHANE H 2 CC1 2 Synonyms: Methylene chloride, methylene dichioride. Des criptiorn Colorless, volatile liquid that boils at 104°F. Penetrating, ethereal odor. Sinks in water; slightly soluble. Nonflammable. Twd city: Local - Irritant, especially to eyes. Systemic - Moderate to severe by all routes; ingestion most toxic route. Aquatic - Moderate to low. WEAR RESPIRATOR AND PROTECTIVE CLOTI{ING. Detection: Commercial detection kits are available; sensitivity range is 25-1000 ppm. Suppliers include MSA and Scott/Davis. Ii, 516). ------- DICHLOROPHENOL 0C 6 H 3 C1 2 N. B. There are six structural isomers, but the 2,4-isomer is apparently the most important. Description: Combustible. white, crystalline solid. Sinks in water; slightly soluble. Acid to litmus. Toxicity: Local - Strong irritant. systemic - Moderate. Aquatic - (Moderate to high). WEAR PROTECTIVE CLOTHING. Detection: Mix 2 nil of sample with 2 ml of 0. 5% 4 arninoantipyrine solution and 2 n-il of 0. 1% sodium carbonate solution. Then add 0. 5 ml of 2% potassium ferricyanide solution and stir well. Positive resuit: solution turns red. This test is widely used for the 2 1 4-dichloro isomer, but may not be valid for all other dichioropheflols. l, 5). ------- DICHLOROPROPANE CIH 2 CC H 2 C Hz Cl Synonyms: Propane dichioride. Description: Colorless, stable, mobile, flammable liquid. Odor similar to chloroform. Sinks; very slightly soluble. Toxicity: Local - Irritant to eyes, skin mucous membranes. Systemic - Low. Aquatic - Moderate. Detection: Commercial detection kits are available; sensitivity is 25 -500 ppm. Suppliers include MSA and Scott/Davis. (1, 5,6 ). ------- DIETHA.NCLAMINE (HOCR 2 CH 2 ) 211(8 Synonyms: His (hydrory ethyl) antine, flEA, diethylolamine, thhydroxythethylaznine, itninodiethanol. Description. Desliquescent white solid which melts at 82°F; usual connnercial form is viscous liquid. Siaks but very soluble. Mild arnxnoniacal fishy odor. Strongly alkaline. Toxicity: Local - Slightly to moderately irritating to skin. Systemic - Low, Aquatic - Reports vary widely, from low to moderate. Other - Raises HOD. Detection: First follow method for detecting MONOETHANCLAMINE. If test is positive and (urther resolution is required, teat for secondary amine (see DIAMYLAMINE) to distinguish from MCNOETHfiSNCLAMINE. ------- DIETHYLAMINE (C 2 H 5 ) 2 Nu Synonyms: None COmmon. Description: flammable, strongly alkaline, colorless liquid. Amniothacaj odor. Floats; very miscible with water. The hydrochloride is also known; it is a hygroscopic liquid, slightly heavier than pare water and soluble in it; its reaction is presumably neutral to slightly acid. Toxicity: Local - Irritating to eyes, mucous membranes, and skin; especiafly irritating by inhalation. Systemic - (Low to moderate). Aquatic - Moderate. Detection: Commercial detection kits are available; sensitivity is 5-ZOO ppm. Suppliers include MSA. (1,5,6 ). ------- DIETHYLENE GLYCOL (HOCH 2 CHz)zO Synonyms: DEG, dihydroxydiethyt ether, oxydiethanol. Description: Clear, colorless, practically odorless, syrupy liquid; non-corrosive and very bygroscopic. Toxicity: Human and aquatic - Practically nontaxic. Other Raises BOO. Detection: There is no simple detection method that can be used at water ’s edge. Instrumental techniques of analysis (such as CC and IRJ are required. ------- DIETHYL PHTHALATE (C 1 H 5 00C) 2 C 6 H 4 Synonyms: DEP, ethyl phthalate. Description: Clear, stable, odorless liquid; bitter taste. Sinks; insolub le. Combustible. Toxicity: Local - Strong irritant to eyes and mucous membranes. Systemic - Moderate by ingestion and inhalation; narcotic in high concentrations. Aquatic - Higb; fish are especially sensitive. WEAR PROTECTIVE CLOTHING; PROTECT EYES. Detection: Use the same methods given for DIBUTYL PHTHALATE. If more specific identification is required and an improvised laboratory is available, use UV spectrometry. ------- DLtSOPROPANOLAMINE (CH 3 CHOHCHz)zNhi Synonym: DIPA. Description: White crystalline solid; ammoniacial fishy odor. Floats and dissolves. The article of commerce is usually a clear, colorless liquid. Toxicity: Local - Irritant; may cause skin burns. Systemic - Moderate to low. Aquatic - Moderate. Detection: Use presumptive test given for MONOETHANOLAMINE (see that entry). If further resolution is required, test for a secondary amine (see the methods given in the DIAMYLAMINE entry to distinguish this compound from MONOETHANOLAM INE. ------- DIISOPROPYLAM INE ((CB 3 )zCH) 2 NH Description: Colorless, volatile, flammable liquid; amine odor. Floats; slightly soThble. Toxicity: Local - Strong irritant. Systemic - Moderate. Aquatic - Moderate. YEAR aESprRATCP ;PROTECTIVE CLOTHING ADVISABLE. Detection: Test for a secondary am ine (see DIAMYLAMINE for methods). ------- DIMETHYLAMJ1 ’ E (C H 3 ) 2 NH Synonym: DMA. Description: Colorless gas at ordinary temperatures; liquefies at 45°F. Very flammable. Strong az-nxncnnacal odor, detectable at a few ppm. Rather soluble in water, giving a strongly alkaline solution. DMA is commercially available as a compressed gas and an aqueous solution (about 40%). Liquid is clear and colorless; gas is heavier than air. Toxicity: Local - Both gas and liquid forms are irritant; can burn skin. Systemic - Low. Aquatic - Moderate. Detection; Commercial kits are available; sensitivity is 5-ZOO ppm. Suppliers include MSA. (1, 5,6). ------- DIMETHYL SULFATE (CH 3 ) 2 50 4 Synonyms: None. Description: Colorless, corrosive liquid which has been used as a war gas. Sinks and dissolves. Toxicity: Local - Highly irritating and corrosive to tissues. Systemic - High; absorbed through the intact skin. Aquatic - (High). Other - Look for corrosion damage. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Commercial kits are available; sensitivity is 1-50 ppm. One supplier is MSA. (1 ,5 ,6). ------- DIMETHYL SULFOXIDE (CH 3 ) 2 S0 Synonyms: DM50, methyl sulioxide. Description: Colorless, nearly odorless, hygroscopic liquid. Slightly bitter taste. Combustible, A powerful solvent that penetrates the skin and other tissues, often causing burns. Toxicity: Local - irritates skin; may cause redness and wheals. Systemic - Low. Aquatic - (Low to moderate). High concentrations may be very damaging to plants as well as animals. Detection: Commercial kits are available; sensitivity is 10-250 ppm. Suppliers include MSA. (1 ,5 .6). ------- D]NLTROBENZENE C 6 H 4 (N0 2 ) 1 Synonynt Dinitrob enzol. Description: White or yellowish crystals that sink in water; very slightly soluble. Toxicity: Local - Strong irritant. Systemic - Moderate to high by inhalation and ingestion; rapidly absorbed through the skin. Aquatic - High. WEAR PROTECTIVE CLOTHING; ERSPIRATOR ADVISABLE. Detection: Extract 10 ml of sample with 5 nil of ether. Let the ether evaporate (WITHOUT HEATING) in open sir, until almost dry. Add 3 ml of acetone and 2 ml of dilute alcoholic NaOH. Positive result: solution turns greenish yellow. Dinitrochlorobenzene, dithtronaphthalene, dinitrotoluene, and dinitroxylene interfere. (1. 5). ------- DINITROPHENOL Synonyms: Aldifen, hydroxydinitrobenzene. Description: Yellowish to yellow crystals, which sublime. Sinks; slightly soluble in cold water, soluble in hot water. Soluble in alkaline solutions. The sodium salt of dinitrophenol is readily soluble in water. Frequently used as a colorimetric pH indicator; it is colorless in strong acid solution, but turns brilliant yellow in dilute acid solutions. Toxicity: Human - rnghJy toxic by all routes, including absorption through the intact skin. Aquatic - High. WEAR PROTECT iVE CLOTRING;RESPIRATOR ADVISABLE. Detection: Mix 2 ml of sample with I ml of 0. ZN stannous chloride in iN NaOH solution. Positive result: crimson for the 2, 5 isomer, violet-blue for the 2, 3 and 3,4 isomers. (1, 5,6). ------- EPJC}{LORO}{YDRIN CH 2 00HCH 2 CI Synonym: Chioroepoxypropane. Descriptiorn Colorless, very volatile, unstable liquid. Sharp odor of garlic. Sinks; practically insoluble. Toxicity: Local - Very irritating; cannot be tolerated in high concentration. Systemic - Moderate to high; narcotic. Aquatic - Moderate to high, especially to bottom life. WEAR RESPIRATOR AND PROTECT iVE CLOTHING. Detection: Mix 5 ml of sample with 10 ml of 22% NaCl solution containing a few drops of phenolphthalein indicator. Heat in a steam bath for 1 minute. Positive result: solution turns pink to red. Neutralize sample before beginning test. (1, 5, 6). ------- ETHYL ACRYLATE CH 2 CHC00CzH 5 Synonyms: None. Description: Clear, colorless, very flammable liquid. Floats; nearly insoluble. Sharp, fragrant odor. Readily polymerized; HYDROQUINONE is frequently added to inhibit polymerization. The polymer is a clear plastic, the common polyacrylate and polyacrylic resin of commerce. Toxicity: Local - A potent jacrimator, very irritating to eyes and skin. Systemic - Moderate. Aquatic - Moderate to low. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: There is no adequately specific test for use at water’s edge. In an improvised laboratory, hydrolyze the ester, then follow detection methods for ACRYLIC ACID (see that entry). As a gross presumptive test, test for unsaturation as follows. (I ). When the acrylate forms a distinct organic phase, separate that phase and add to it a few drops of bromine in carbon tetrachloride (approximately 1%). Positive result: the reddish-brown bromine color disappears. (1,3). (U). When there is no distinct organic phase, add a few drops of aqueous potassium permanganate solution (about 1%). Positive result: the purple permanganate color disappears. (1, 3). ------- ETHYL ALCOHOL C 2 H 5 OH Synonyms: Cologne spirits, ethanol, ethyl hydroxide, ethylic alcohol, fermentation alcohol, grain alcohol, Lavacol, methyl carbinol, neutral spirits, proof spirits, spirit of wine. Description Clear, colorless liquid. Completely miscible with water, flammable even when mixed with some water. The pure substance has well-known taste and odor, but industrial and antiseptic grades are denatured with a variety of unpleasant substances which greatly alter the taste, odor, and toxicity. Toxicity: Local - None. Systemic - Drunkenness by ingestion; denatured grades are toxic by ingestion. Aquatic - Low to moderate, depending on the denaturants and their concentration. Various salts of MERCURY are frequently used as denaturants; they are bio- accumulative poisons. Detection: Several commercial kits are available for detection; sensitivity is 200-5000 ppm. Suppliers include Kitagawa, MSA, and Scott/ Davis. (1, 516). ------- ETHY LAMINE CH 3 CH 2 NH 2 Synonyms: Amino ethan e, mono ethylarnine. Description: Colorless flammable, volatile liquid which vaporizes at 63°F. Ammoniacal odor. Floats, but dissolves quickly, forming a strongly alkaline solution. Toxicity: Local - Very irritating to eyes, mucous membranes, and skin. Systemic Moderate by ingestion. Aquatic - Moderate. PROTECT EYES FROM VAPOR AND LiQUiD; RESPIRATOR ADVISABLE. Detection: Commercial kits are available for detection; sensitivity range is 10- 500 ppm. Suppliers include MSA. (1, 5 ,6). ------- ETHYL BENZENE $ynonyins Ethyl benzol phenylethane. Description: Colorless flammable liquid that smells like benzene. Flash point at 85°F. Floats; slightly soluble. Toxicity: Local - Vapor and liquid are slightly irritating. Systemic - Low . Aquatic - Moderate. Detection: If an improvised laboratory is available, use IJV spectrometry for the identification. Ethyl benzene has distinctive absorption between 290 and 247 miii- microns. As a gross presumptive test, test for an- saturation (see ETHYL ACRYLATE for recommended methods). ------- ETHYLENE CH 2 :CH 2 Synonyms: Bicarburetted hydrogen, elayl . ethene, etherin, heavy carburetted hydrogen, olefiant gas. Description: Colorless gas or liquefied gas under pressure. Very weak, sweetish odor. Vaporizes very quickly. Very flammable, Floats; slightly soluble. Toxicity: Human - Virtually nontoric. Aquatic - Moderate to high; some fish are very sensitive. Detection: Cornniercial detection kits are available; sensitivity range is 0. 5-100 ppm. Suppliers include Kitagawa, MSAJ, and Scott/Davis. (1,4,6). ------- ETHYLENE CYANOHYDRIN }JOC 2 H 4 CN Synonyms: Cilycol cyanohydrin, hydrac rylonitrile, hydroxypropionitrile. Description; Colorless to straw- colored liquid. Sinks, but completely mis cible. Tot city: L .oca i. — None. Systemic — Low. Aquatic - Low. Detection: See ACETONE CYANOHYDRIN for recommended method. The method given there applies without change to this compound. ------- ETHYLENEDIAMINETETRAACETIC ACID (HOOCCHz) 4 NC 2 H 4 N Synonyms: 1 DTA, ethylenebisiminodiacetic acid, ethyleneth- nitrilotetraacetic acid. Description: Cojorless crystals; sink and slowly dissolve iz water. A powerful chelating agent. Several common rnetaflic salts are called Tedetatestt; they are very soluble in water. EDTA and the edetates are widely used in detergents, agriculture, industry, and medicine. Toxicity Human - LOW. Aquatic - Moderate. Detection: Commercial detection kits are available; suppUers include 1-Itch and Larnotte. (2, 5 ,6 ). There is also a simple and sensitive wet-chemical test. Add 5 nil of 0. 05M cobaltous nitrate solution to S ml of sample. Mix and then add a few drops of 0. 05 ) 4 ferric chloride solution. Positive result: solution turns red. (2 .4,6). ------- ETHYLENE GLYCOL HO{CH 2 ) 2 0H Synonyms: Ethanediol, ethylene alcohol, dihydroxyethane. Description: Clear, colorless, hygroscopic, flammable liquid. Sweet taste and weak, sweet odor (like antifreeze). Sinks and dissolves readily. A common antifreeze. Toxicity: Local - None Systemic - Low. Aquatic - Low. Other - Raises SOD; this is the major problem. Detection: The recommended detection method requires an ice bucket for cooling. Mix S ml of sample with 2. S ml of 6. 6% sodium periodate solution. Cool to 32°F, then add 1 ml of saturated potassium nitrate solution. Add 2 nil of 1% aqueous phenyihydrazine hydrochloride and 1 ml of 2% potassium ferricyanide. Cool again to 32°F , then add S nil of chilled concentrated HC1. Positive result: solution turns red. Sorbitol inter- feres. (1,5.6). ------- ETHYLENE CiLYCOL DIACETATE CH 3 GOOCHzCHzO 3 Synonym: Glycol diacetate. Des cription: Colorless liquid. Faint odor. Burns. Widely used solvent. Sinks and dissolves. Toxicity: Human - Low. Aquatic - Low. Other - Raises SOD. Detectiorn There is no suitable method for detection at water’s edge. In an improvised laboratorY use CC. ------- flHYLENE GLYCOL MONOBUTYL ETHER OH(CH 2 ) 2 0C 4 H 9 Synonyms: B utoxy ethanol, biatyl cello solve. Description: Colorless liquid with a mild odor, floats and dissolves. In general, an inert solvent for both water and organics. Toxicity: Human - Low. Aquatic - Low. Detection: there is no suitable method for detection at water’s edge. In an improvised laboratory, use CC. ------- ETHYLENEIMINE H 1 CNI ICH 2 Synonyms: AZ ac yclopropane, aziridine, thmethyleneimine. Description: Clear, colorless liquid. Strong, fishy amine odor. Floats and dissolves readily. Very strongly alkaiine and corrosive. Caution extremely flarrunable, and polymerizes with explosive effect. An inhibitor (presumably HYDROQUINONE ) is often added to control spontaneous polymerization. Toxicity: Local - Vapor extremely irritating; liquid causes severe burns. Systemic - 1-Ugh by all routes, including skin absorption. Aquatic - Moderate. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detectioa; Commercial ldts are available; sensitivity range is a—mo ppm. One supplier is MSA. (1, 5 ,6). ------- FERRIC CHLORIDE FeC I 3 Synonyms: Ferric terchioride, ferric trichloride 1 fibres rnartis, iron chloride ron perchioride, iron trichioride. Descriptiont The anhydrous solid is blackish brown; the crystalline form is orange-yellow and very deliquescent. Sinks and dissolves , but decomposes spontaneously to yie ld HYDROCHLORiC ACID and FERRIC HYDROXIDE when exposed to moist air and light. Tothcity: Human - Low. Aquatic - Highly variable, from High to Low. Detection: The Fe and Cl components must be separately analyzed. See FERRIC HYDROXIDE for Fe methods. See AMMONIUM CHLORIDE for C l methods. ------- FERRIC HYDROXIDE Synonyms: Ferric hydrate, iron hydroxide, iron hydrate, iron oxide (hydrated), ferric oxide (hydrated). Description: Brown to reddish brown solid, often as a flocculant precipitate. Sinks; aimost insoluble. Toxicity: Human - Low. Aquatic - Moderate to high. Detection: Prepare suspect solids for testing by dissolving in 3M HCI. then proceed as follows. ( I). Mix the sample with 1% arnmoniurn thiocyanate solution. Positive r e suit: solution turns intensely red. (U). Mix the sample with 1% potassium ferrocyanide solution. Positive result: deep blue solution or precipitate. Since many waters and bottom solids are high in iron, background may be very high. (2, 5,6). Several commercial kits are available for detecting dissolved iron; suppliers include Lamotte, Taylor, Refuge, and Hach. (2,5,6). ------- FERRIC SULFATE Fe 2 (504)3 Synonyms: Ferric sesquisulfate, ferric trisulfate, iron persulfate, iron sulfate, iron tersulfate. Description: The anhydrous form is a grayish white powder; the crystalline form Is yellow. Both forms sink but the crystals are very soluble, while the anhydrous form is slightly soluble. Totcity: Human - Low. Aquatic - Moderate to high. Detection: The Fe and SO 4 components must be separately analyzed. See FERRIC HYDROXIDE for Fe methods. See ALUMINUM SULFATE for SO 4 methods. ------- FERROUS HYDROXIDE Fe(OH)- , Synonym: Iron hydroxide. Description: White crystals, which may have a tinge of green. Sinks; almost insoluble. Spontaneously converted to FERRIC HYDROXIDE on exposure to air , but the conversion is slow unless the material is very finely thvided. Toxicity: Human - Low. Aquatic - Highly variable, from High to Low. De t ection: Since this compound spontaneously becomes FERR IC HYDROX iDE on exposure to air, lest for ferric iron by the methods given in the FERRIC HYDROXIDE entry. Ferric iron is reconverted to ferrous iror when it is mixed with 3M H,5O 4 . Test for ferrous iron by either of the following methods. c i i. MS the sample with 0. 5% pOtassium ferricvanide. Positive result: deep blue solution or precipitate. (2, 5. 6’ . ill)- Mix the sample with a 2t ! Ø alcoholic 2. 2 ’ -dipyridyl (or 1,1- ..phenanthrolinei solution. Positive result: solution turns red or pink. (2, 5, 6). ------- FERROUS SULFATE FeSO 4 Synonyms: Copperas, green vitriol, iron sulfate, iron vitriol, sa l chalybdis. Description: Industrial grades are greenish or yellow-brown hygroscopic crystals or granules. Pure grades are white, yellow, or blue-green, depending on hydration. Odorless. Sinks; slightly soluble. Salty taste. Slowly oxidized to FERRIEC SULFATE in air. Totcity: Human - Low. Aquatic - Highly variable, from High to Low. Detection: Ferrous iron is converted to ferric iron in air. Test for both ferrous arid ferric forms. The iron and sulfate components must be analyzed separately. See FERROUS HYDROXIDE for ferrous methods. See FERRIC HYDROXIDE for ferric methods. See ALUMINUM SULFATE for SO 4 methods. ------- FERROUS SULFITE FeSO 3 Synonyms: None common. Description: White or greenish crystals. Sinks and dissolves. Slowly oxidized to the corresponding ferric salt Toxicity: Human - Low. Aquatic - Moderate. Detection: The ferrous and sulfite components must be separately analyzed. See FERROUS HYDROXIDE for ferrous methods. Detect sulfite a , follows. Mis 1 ml saturated Zn(N0 3 ) 2 with 1 ml of iN K 4 Fe(CN) 6 solution. Add to this 1 ml of 1% sodium nitroprusside solution; a white precipitate MU form. Then add 1 ml of the sample. Positive result; the white precipitate turns red. (l 5,6). There are several commercial detection kits for sulfltes; suppliers include Larnotte, Taylor, Hei.lige, and HaS (1 4,6). Sensitivity range is 2-300 ppm. ------- FLUORINE Fz Synonyms: None common. Description: Pale, greenish-yellow gas, usually sold commercially as an extremely cold (- 306°F) liquefied gas, which is clear to yellow. Strongly acid to litmus. Highly reactive at room tempera- ture. Reacts with water to form HYDROFLUORIC ACID, HYDROGEN PEROXIDE, ozone, oxygen, and oxides of fluorine. Toxicity: Local - Extremely irritating to eyes, lungs, and skin. Liquid causes severe skin and eye burns. Systemic - High. Aquatic - High. YEAR RESPIRATOR AND PROTECTIVE CLOTHING. Ddection: See HYDROFLUORIC ACID and HYDROGEN PEROXIDE for the detection methods applicable to FLUORINE’S reaction products with water. ------- FORMALDEHYDE HCHO Synonyms: Formalin, formic aldehyde, Lormol, methanal, oxyrn ethylene. Description: ColorIess very flammable gas, with a suffocating, biting odor. The gas is readily water soluble, and is usually sold as a 37-50% solution. The aqueous solution is not flammable, but it releases flammable gas. Be- cause formaldehyde polymerizes, it is often mixed ‘with METHANOL (about 15%) to inhibit polymerization. Toxicity: Local - Gas very irritating. L iquid causes burns. Systemic - Moderate. Aquatic - Moderate. WEAR RESPiRATOR AND PROTECTIVE CLOTHING. Detection: Commercial kits are available; sensitivity range is 1-100 ppm. Suppliers include MSA and Scott/Davis. (1 5, 6). ------- FORMIC ACID HCOOH Synonyms: Hydrogen carboxylic acids niethanoic acid. Description: Colorless, fuming acid. Sharp, biting odor. A strong acid, dangerously caustic. Acid to litmus. Sinks; completely miscible. Combustible. Toxicity: Local - Irritant vapor; liquid causes burns. Systemic - Moderate. Aquatic - Moderate; not toxic to fish except insofar as it affects pH and osmotic pressure. Other - Look for corrosion effects. WEAR RESPUtATOR AND PROTECTIVE CLOTHING. Detection The recommended method requires an ice bucket (or equivalent) for cooling. Mix I ml of sample with 0. 1 g of magnesium ribbon. Immerse in an ice bath, then add dropwise, at one-minute intervals, 10 drops of concentrated HCI. Finally, add I ml of 0. 3% chromotropic acid in 1 IM sulfuric acid. Positive result: a white precipitate forms, and the solution turns green or yellow. (1,5,6). ------- FRUCTOSE Synonyms: Fruit sugar, levulose. Description: White crystals or powder. Sinks and dissolves. The sweetest of the common sugars. Combustible. Tox icity: Human and aquatic -. Practicafly nontoxic. Other - Raises BOD. Detection: Test the sample by the following methods. Each method is presumptive 1 but taken together they build up a fairly conclusive case for the presence of fructose. (1). Mix zm lofsamplewith2nilof0.l% ethanolic resorcinol and 6 ml of con- centrated HC1 containing 0. 75 mg of ferric chloride per 100 ml. Heat in a water bath. Positive result: solution turns cherry red. (1, 5, 6). (U). Mix 1 nil of sample with 10 ml of 4% ammoniurn molybdate. Add 0. 25 ml of 1:3 nitric acid and heat at 150°F for 3 minutes. Positive result: solution turns blue. (1, 5,6). (II I ). Mix 1 ml of sample with 0.4 ml of 0. 2% aqueous orcein solution and I ml of 85% phosphoric acid. Heat in boiling water for 10 minutes. Positive result: solution turns yellow and/or a yellow precipitate forms. (1,5,6). ------- E LIMARIC Ac m HOOCCH CHCOoH Synonyms: AUomaleic acid, boleic acid, trans-butenedioic acid, trans-ethylenedicarboxylic acid, lichethc acid. Description: Colorless, odorless crystals or leaflets. Sinks; practically insoluble in cold water, but moderately soluble in hot water. Tastes like fruit acid. Toxicity: Local - Irritates eyes and skin. Systemic - Low. Aquatic - Low. Other - May increase BOD. Detection: There is no adequately specific test for use at water t a edge. Use the following gross pres umptive test for unsaturation. To Z ml of sample add several drops of 1% aqueous KMnO 4 . Positive result: the purple permanganate solution is deco iorized. (1, 3,6). ------- FtJRFTJRAL OCThCHCThCCHO Synonyms: Artificial oil of ante furaldehyde, pyromucic aldehyde. Description: Colorless, mobile, oily liquid when pare; turns yellow to reddish brown on exposure to ligbt and air. Penetrating odor like almond oil. Slowly resinifies on exposure to the elements. Combustible. Toxicity: Local - Irritant vapor. Systemic - Moderate. Aquatic - Moderate. Detection: Mix 2 ml of sample with 2 ml of 0. 5% oxalic acid containing 1% of disodiuni phosphate. Then add 3 ml of 10% aniline in glacial acetic acid. Positive result: solution turns red. (I, 5 6) ------- FURFURYL ALCOHOL OCH:CHCH:CCH 2 QH Synonyms: Furanecarbinol, furfuralcohol, 5u ryl carbinol, hydroxyni ethylfu.r an. Description: Colorless, mobile liquid; becomes dark red or brown on exposure to light and air. Sinks; very soluble in water, but decomposes. Solutions of furfuryl alcohol that have been exposed to air and light, or those that have been standing (or some time, are almost insoluble in water. Toxicity: Local - Slightly irritating liquid and vapor. Systemic - Moderate to low. Aquatic - Moderate. Detection.; Commercial kits are available for detection; sensitivity range is Z5-500 ppm. MSA is one supplier. (2, 5,6). ------- GALLIC ACID (OH ) 3 C 5 H 2 C00H Synonym: Tnliydrozybenzoic acid. Description: Colorless or slightly yellow crystals. Sinks; sparingly soluble. Toxicity: Human - Low. Aquatic - Moderate. Detection: Add dilute £erric chloride to the sample. Positive result: dark blue solution and precipitate. (l 5, possibly 6). ------- GLUCONIC ACID CHzOH(CHOH) 4 COOH Synonyms: Glycogenic acid, glyconic acid. Description: Light brown syrup with niildly acid taste. Faint odor of vinegar. Sinks and dis solves. Toxicity: Human and Aquatic - Practically nontoxic. Other — Raises BOD. Detection: There is no suitable method for detection at water’ s edge. In an improvised laboratory the acid may be esterified and the ester identified by CC. ------- GLUCOSE C 6 H 12 0 6 Synonyms: Corn sugar, corn syrup, dextrose, grape sugar, starch syrup. Description: The pure substance is a white crystal, but commercial forms include syrups that vary from clear and colorless to dark brown and opaque. Sinks and dissolves. Toxicity: Human and Aquatic - Practically nontoxic. Other - Raises BOIl. Detection: Use any of the following presumptive tests. Many other sugars will test positive 1 but these tests are sufficient for damage assessment. (1 ). Mix 1 ml of sample with a ml of 0. 18 potassium ferricyanide and 2% sodium carbonate. Positive result; solution turns blue. (1,SI6). (U). Mix 1 ml of sample with Z ml of 0. 27% KH,P0 4 and 4 ml of 7.. 5% ammonium motybdate. Positive result: solution turns blue. (1, 5,6). (U I ). Mix 5 ml of sample with 5 ml of 5% KOH and 2 ml of 1% sodium biselenite. Positive result: a colloidal precipitate. (1, 5,6). ------- GLYCEROL H 2 COHCHOHCH 2 OH Synonyms: Glycerine, glycyl alcohol, propanetriol. Description: Clear, colorless to pale yellow, odorless syrup. Sweet, warm taste. I4vgrosconic. Sinks: rniscthle. Toxicity: Human and Aquatic - Practically :mtoxic, Other - Raises B aD. Detection: Each of the following methods is a presumptive test for glycerol. Taken together, they build up a fairly conclusive case for the presence of glycerol. U). Mix 1 ml of sample with .1 ml of 1:1 Add a few drops of 7. 5% potassium bichromate solution. Positive result: decolorization of the orange bichromate solution. ti , 4 , 6). UI). Mix 4 ml of sample with 1 ml of 5% codeine in ethanol. Add S ml of 1:3 1-12504. Heat for minutes in boiling water. Positive result: 5olutiOn turns blue. fl,4, b). Mix 1 ml of sample with 1 ml of freshly prepared 10% catechol solution and 4 ml of 3:1 H 2 S0 4 . 1-feat in boiling water for 15 minutes. Positive result: solution turns red , U, 4, 6). ------- HEPTANOIJ C 7 H 15 0H Synonyms: Heptyl alcohol, hydroxybeptane, enanthyl alcohol, methyl arnyl carbinol. Descriptionz There are 3 important isomers. All are colorless . fragrant liquids that float and are slightly soluble. May cause flowing water to froth. All are flammable. Totcit Htunan - low to moderate, depending on isomer. Aquatic - (Moderate). Detection: Use grass presumptive test for aliphatic alcohols. See BtJTYL ALCOHOL for recoznmexxied methods. ------- HEXAMETI- IYLENE DIAMINE H 2 N(C H 2 ) 6 NH 2 Synonyms: Diaminohnane hexane diamine. Description: Colorless leaflets that are very soluble in water. Toxicity: Local - Strong irritant. Systemic - Moderate by ingestion. Aquatic - Moderate. PROTECTWE CLOTHING ADVISABLE. Detection: Use gross presumptive test for primary arnines. See PROPYLAMINE for recommended methods. ------- HEXANOL C 6 H 13 0H Synonyms: Amyl carbinol, hexyl alcohol. Description: Only then isomer is common. Colorless liquid. Floats; slightly soluble. Combustible. Toxicity: Human - Low. Aquatic - Moderate. Detection: Use gross presumptive test for aliphatic alcohols. See BTJTYL ALCOHOL for recommended methods. ------- IIYDRAZII4E H 2 NNH 2 Synonym; Diaxnine. Description: Colorless, fuming, hygroscopic, extremely flammable liquid. Strong odor. Miscible with water; may sink or float depending on water; sinks in clean fresh water. Weakly basic. Toxicity: Local - Vapor and liquid are strong irritants that may cause burns. Systemic - Moderate. May be absorbed through intact skin. Aquatic - High. WEAR RESPIRATOR AND PROTECTIVE CLOTHiNG. Detection: Commercial test kits are available; sensitivity range is 0. 0-0. 5 ppm. Suppliers include Hach, HeUige , and Lamotte. (2, 5,6). lf test kit is not available, mix I ml of sample successively with: (1) 1 ml of 1% aqueous pyridylpyridinium chloride, (2) 1 ml of IN NaOH, and (3) 1 ml of concentrated HC1. Positive result: solution turns red. (1, 5). ------- HYDROCHLORIC ACID HC1 Synonyms: Hydrogen chloride, muriatic acid. Description: Clear, colorless to slightly yellow, fuming, acrid liqiAd. Cannot catch fire. Strongly corrosive: a powerful acid that is easily detected by litmus and other indicators. Miscible with water. Toxicity: Local - Kwtremely irritating vapor, liquid causes burn s. Systemic - Moderate. Aquatic - Moderate. Other - Look for corrosion effects. Detection: Commercial kits are available; sensitivity range is 2-1.000 ppm. Suppliers include Hach,, Hellige, Lamotte, MSA, sod Scott/Davis. (1, 5,6). Because this is one of the strongest acids known, pJ-t papers and pH meters ‘nay be used to monitor the spill. In strongly alkaline waters, use the test for the chloride ion to detect dilute solutions; see AMMONIUM C ORIDE for recommended method. ------- HTDROCYAMC ACID HCN Synonyms: Formothtrile, hydrogen cyanide, prus sic acid. Description: Colorless liquid that vaporizes at 79°F. Very soluble. The gas is lighter than air and the liquid is lighter than water, but is miscible. Very weakly acid; doesn’t redden litmus. The rising vapor is very toxic and explosive. Widely used in rodenticides and insecticides. Characteristic odor of bitter almonds, which is detectable at a few parts per miflion. Intensely Poiso us . Totcity: Human - High. Aquatic - High. Toxic to Esh and plankton. YEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Commercial kits are available for detection; sensitivity range is 2-3000 ppm. Suppliers include Kitagawa. MSA, Mach , and Scott/Davis. (1, 5, 6). ------- HYDROFLUORIC ACID HF Synonyms: None common. Description: Clear, co]orless to slightly tinted, fuming, mobile liquid. Sharp odor. Will attack glass, rock, sand, or any other material that contains silica. Completely miscible with water. Cannot catch fire. Toxicity: Local - tremely irritant to eyes, skin, lungs. Systemic - High. Toxic by skin penetration. Aquatic - High to moderate. Other - Look for corrosion effects in rocks, sand, and other silica-bearing materials. WEAR R PIRATOR AND PROTECTIVE CLOTHING. Detection: For gross detection of acidity, use pH papers or pH mder. For more specific detection, use any of the conimerciaily available kits; sensitivity range is 0. Z-7. 5 ppm. Suppliers include HeRige, Larnotte, MSA, and Scott/Davis. (1, 5,6). ------- HYDROGEN PEROXIDE HOOH Synonyms: Albone, Hydrogen dioxide, peroxide, superoxol. Description: Colorless, heavy liquid, usually sold in aqueous solution (various strengths). Very unstable; breaks down readily into water and oxygen. Commercial solu- tions often contain a decomposition inhibitor, e. g. acetophenidin or acetanilide. Bitter taste. A strong oxidizing agent. Toxicity: Local - Strong solutions (35% and higher) are irritant. Systemic - Moderate. Aquatic - Moderate. Other - Look for bleaching and strong evidence of oxidation. Detection: Mix sample with 1N HC1, then add several drops of 1% KMnO 4 . Positive resuit: the purple permanganate solution is bleached. (1, 3,6). ------- HYDROQU WONE C 6 H 4 (OH)z Synonyms: Bensenedjol, hydroquinol, paradihydroxybensene, quinol, Tecquinol. Description: Conthustible white crystals that sink and dissolve. Unstable in the presence of air and light. Aqueous solutions turn brown in air. Totcitr Local - Irritant; can sensitize skin. Systemic - Moderate. Aquatic - Moderate to high. Detection Extract 10 ml of sample with 5 ml of ether, then separate the ether layer. Mix the ether layer with 5 ml of 1:1 XM l ) 3 . Let it stand for 5 minutes, then dilute with 10 ml of water. Carefully sake basic (alkalify) with 10% NaOH. Positive result solution turns violet. (1. 5). ------- HYDROXYLA.Mfl s IE NHzOH Synonyms: Oxanunoniurn. Description: Unstable white flakes or crystals that sink and dissolve. Very hygroscopic. Rapidly decomposes at room temperature, especiaUy in the presence of oxygen and carbon dioxide. Alkaline reaction. The acid sulfate, hydrochloride, and sulfate are common derivatives. Toxicity: Local - Irritant. Systemic - Moderate. A KNOWN CARCINOGEN. Aquatic - Moderate . Detection: Mix Z ml of sample with 2 ml of IN HC1. Add to it 0 ,1 g of afloxan and 0.1 g of sodium carbonate. Positive result: solution turns violet. (1, 5. possibly 6). ------- HYPOCHLOROUS ACID HOC1 Synonyms: None common. Description: Greenish-yellow aqueous solution. Highly unstable, weak acid; pH not a reliable indicator. Decomposes to HYDROCHLORIC ACID and oxygen. Can exist only in dilute solution. Very corrosive. Toxicity: Local - Irritant. Systemic - Moderate. Aquatic - Moderate for fish and animal life; highly toxic to plants and algae. Other - Look for corrosion and bleaching effects. Detection: Test for the hypochiorite ion as foUows Prepare 2 samples in separate teat tubes. To 1 tube add a 0. 1% solution of indigo, drop by drop. To the other tube add 0. O1N KMnO 4 solution, drop by drop. Positive result: the indigo solution is decolorized, but the permanganate soluUon is not. (1 , 5,6 - - animals only). Also refer to tests for HYDROCHLORIC AC ! !) and the chloride ion (see AMMONIUM CHLORIDE). ------- INDOLE (CH) 4 CC(CH) 2 NH Synonyms: Benzopyrrole. )escription: White to yellowish scales which turn red on exposure to air and light. In high concentration, the odor is unpleasant and fecal; in dilution, the odor is pleasant. Sinks; slightly soluble. Toxicity: Hu man - Carcinogenic. Other effects probably low. Aquatic - High. )etection: Mix I nil of sample with 1 ml of 5% xanthydrol in ethanol and 4 ml of glacial acetic acid. Heat in boiling water for 5 minutes. Positive result: solution turns reddish violet. (2, 5). ------- ISOPRENE H 2 C:C(CH 3 )GH:CH 2 Synonym: Methyl butadiene. Description Glen, colorless, volatile liqui& Mild, aromatic odor. floats; insoluble. Highly flanunable. To.tcity: Local - Liquid and vapor are irritant. Systemic - Moderate. Harmful vapor. Muatic - Moderate. WEAR RESPIRATOR. Detectiorn Test for butadiene moiety. See CHLOROBUTADIENE for method. ------- LACTIC ACID H 3 CCHOHCOOH Synonyms: Hydroxypropanoic acid, milk acid. Description: Colorless to yeUowish, odorless, hygroscopic synp. Sinks; miscible with water. Acid to litmus. Toxicity: Local - Mildly irritant. Systemic - Low to moderate. Aquatic - Moderate. Other - May raise BOD. Detection: 3 steps are required for detection. (1). Test the sample for FORMALDEHYDE (see that entry for detection kits). This test must be negative, or there is no point to proceethng FORMALDEHYDE is a hazardous material too. (2). Evaporate almost to dryness 5 ml of sample. Let cool and add 1 nil of concentrated 112504. Dilute with 10 tnt of water. (3). Test for FORMALDEHYDE again. Positive result: step (3) is positive for FORMALDEHYDE, but step (1) is negative. (1,5,6). ------- LACTOSE C 1 2 Hz 2 O 1 1 Synonyms: Milk sugar, saccharum lactis ,. Descriptiorn Hard white crystalline mass or white powder. Faintly sweet taste; odorless, but readily absorbs odors. Sinks and dissolves. Toxicity: Human and aquatic - Practically norttoxic. Other - Raises BOX), Detection: Heat Z ml of sample for one minute with 2 m i of 5% KOH in boiling water bath. Positive result: solution turns red-brown. Many other substances interfere. 1, 4, 6). ------- LANTHANUM ACETATE La(C 2 1i 3 0 2 ) Synonyms: None. Description: Water-soluble white powder. Toxicity: Human - Low. Aquatic - High. Detection: Add 2 ml of sample to 3 ml of dilute acetic acid and 1. ml of 0. OW iodine solution. Positive result: dark blue precipitate. (1, 5). This test for lanthanum is the complement of the lanthanum test for acetate. See AMMONIUM ACETATE for details of method. (1, 5). ------- LEAD ACETATE Pb(C 2 H 3 O 2 ) 2 Synonyrm Sugar of lead. Description: White crystals or flakes, when pure; commercial grades are frequently brown or grayish lumps. Sinks and dissolves, but absorbs CO 2 from air, becoming insoluble. Combustible. Toxicity: Local - Irritsflt. Systemic - Lead is a cumulative poison. Moderate. Aquatic - ifigh. Detectiorn The lead and acSate components must be separately analyzed. See AMMONIUM ACETATE for acetate methods. To detect lead, mix 1 ml of sample with 2 ml of 5N KCN and 1 ml of concentrated NR 4 OH. Add 4 nil of saturated dithisone in CC1 4 solution. Positive result tetrachioride layer turns red. Ferric ion and phosphate interfere. (1, 5). N. B. Many natural conditions will bring about the precipitation of lead from s&ution. Be certain to examine surface bottom deposits. To redissolve metals in bottom solids, boil in aqua regia, mter discard precipitate, and test filtrate as above. ------- LAD ARSENATE Pb 3 (As0 4 ) 2 pionym: Lead orthoarsenate. escripdon: White crystals or heavy white powder. Sinks; almost insoluble. A constituent of several types of pesticides. :ari city: Local - May irritate eyes and skin. Systemic - Cumulative poison. Moderate. Aquatic - High. dection: The Pb and As0 4 components must be analyzed separately. See LEAD ACETATE for Pb methods. To detect As0 4 , place in a test tube 1 ml of sample, a few grains of metallic zinc, and 5 drops of 6M H 2 5O 4 . Loosely plug the tube with cotton that has been soaked in 1ON 1-IC1. Then cover the tube with filter paper that has been impregnated with 20% AgNO 3 . Positive result: the filter paper turns brown-black. (1, 5, 6). ------- LEAD CHLORIDE PbCI 2 Synonyms: None common. Description: White crystals. Sink; slightly soluble. Toxicity: Human - A cumulative poison. Moderate. Aquatic - High. Detection: See LEAD ACETATE for Pb methods. See AMMONIUM CHLORIDE for Cl nxethods Since the Pb is much more important than the Cl , consider dissolving suspect bottom solids in boiling aqua regia to dissolve any lead present. ------- LAD NITRATE Ib(N0 3 )z synonyms : None common. )escription: White crystals that sink and dissolve. The aqueous solution is slightly acid. roxicity: Local - Astringent; irritant in high concentration. Systemic - Cumulative poison. Moderate. Aquatic - High. Detection: The Pb and NO 3 components must be analyzed separately, but the Pb is much more important. See LEAD ACETATE for Pb methods. See AMMONIUM NITRATE for NC 3 methods. ------- LEAD SULFATE PbSO 4 Synonyms: Anglesite, lanarkite. Description: Heavy, white crystals. Sink; almost insoluble in cold water. Toxicity: Same as LEAD CHLORIDE. Detection: See LEAD ACETATE for Pb methods. Treat solid samples with concentrated NaOH, which will dissolve any PbSO 4 present as undissolved solid. See ALUMINUM SULFATE for 504 methods. ------- LEAD T ETRAETHYL PbR 4 Synonyrn Tetraethyl lead. Includes: Mixed lead alkyls . e. g. • various methyl and ethyl derivatives. Description: Heavy colorless liquid, frequently tinted with a dye. Sweet odor. Sinks; almost insoluble. Decomposes slowly at room temperature. A principal ingredient of motor fuel antiknock compounds. Toxicity; Human - Moderate to high by all routes, including inhalation and skin absorption. Aquatic - High , WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection This substance is just soluble enough to yield a positive response to the Pb method recommended at the LEAD ACETATE entry. For higher concen- trations of Pb ion, reflux 2 ml of sample with 5 ml of 6N HNO 3 . After a clear solution is obtained, let cool and dilute with 50 ml of water. Then test for Pb as above. ------- LINOLEIC ACID C 18 diunsaturated monocarboxylic acid Synonyms: Linolic acid, octadecandienoic acid, a major ingredient of linseed oil, safflower oil, and taU oil. Description: Colorless to straw-colored oil, easily oxidized by air. Floats; practically insoluble. The sodium salt is a common soap, very soluble, and a good sudsing agent. Toxicity: Human - Practically nontotc: an edible oil. Aquatic - Variable, from very low to very high. Detection: Use unsaturated sites as presumptive test. For a distinct organic phase of supernatant oil, add a few drops of bromine in carbon tetrachloride (about 1%). Positive result: bromine is decolorized. For the dispersed aqueous phase (especially for the sodium salt), add a few drops of 1% aqueous KMnO 4 . Positive result: the permanganate color disappears. Other unsaturated organics and strong redoxing agents interfere. (1, 3). ------- LITHIUM CHLORIDE L1C 1 Synonyms: None. Description: White deliquescent crystals, very soluble in water. Sharp salty taste. Toxicity: Human - Low. Aquatic - Low. Detection: Detect Li ion as follows. Mix 2 ml of sample with 10 ml of amyl alcohol. Evaporate the mixture on a hot plate (ABSOLUTELY NO FLAME) until all the water has been expelled. Filter arid add. the filtrate to 2% ammonium stearate in amyl alcohol. Positive result: precipitate forms. (1, 5,6). ------- MALEIC AC m HOOCCIbCHCOOH Synonyms: Cisbutenedioic acid, maleinic acid toxilic acid, ethylene dicarboxylic acid. Descriptiorn Colorless crystals. Very soluble Lu water. Faint odor; repulsive astringent taste. Combustible. Acid to litmus. Toxicity: Local - Very irritant; sensitizes skin and respiratory tract. Systemic - Low. Aquatic - Moderate. PROTECTIVE CLOTHING ADVISABLE. Detectiorn Only conctrated solutions can be reliably detected by pH. For dilute solutions, use test for unsaturation as follows. Add to 5 ml of sample a few drops of 1% KMnO 4 (aqueous). Positive result the perrnanganate is decolorized. Other unsaturated organics and strong redoring agents interfere. (1, 3). ------- MLEIC ANTHYDRIDE HC:CHC(O)OC(O) Synonyms: Cisbutenedioic anhydride, furanectione , toxilic anbyctride. )ncription: Colorless needles that sublime readily. Floats, hydrolyzing slowly to form MALEIC ACID. Toxicity: See MALEIC ACID. )etection: See MALEIC ACID. ------- MALTOSE Synonyms: Maltobios e, malt sugar. Description: Colorless crystalline solid. Sweet taste; odorless. Sinks and dissolves. Combustible. Toxicity: Human and Aquatic - Practically norttoxic. Other - Raises 801). Detection: Detect as a sugar. See GLUCOSE for method? ------- IETHANETHIOL H 3 CSH ‘nonyms: Methyl mercaptan, merc aptomethane, thiomethyl alcohol, methyl sulfhydrate. )escription: Colorless, flammable gas with very powerful unpleasant odor (like rotten cabbage) at room temperature. Colorless liquid below 43°F. Floats; slightly soluble. The sodium salt is water soluble; the copper salt is practically insoluble. tcity: Local - Strong irritant. Systemic - Low, but high concentrations are narcotic, and the odor is often nauseating. Aquatic - High. Other - Damages plants and phytoplankton as well as fauna. P1RATOR ADVISABLE. tction: The unpleasant odor is detectable by the unaided nose down to a few ppm. Simply heating a few ml of sample should be sufficient to produce enough odor for detection. Also see BUTYL MERCAPTAN. (1,4, 63. Commercial kits are available for detection; sensitivity range is 5-120 ppm. One supplier is Kitagawa. (1,4 or 5,6). ------- MflRA.NOL 14 3 C0H Synonyms: Carbisiol, methyl alcohol, wood alcohol, wood spirit. Des cri$iom Clear, colorless, mobile highly polar liquid. Miscible with water. flammable (flash point is 54°F). Technical grades may have a repulsive odor. Toxicity : Local - May Irritate. Dries skin. Systemic - Low, but high concentration.. may cause bJftudne.s. Toxic effects by aU routei. Aquatic - Low. Detecfion Commercial kits are available; sensitivity range is 100-10,000 ppm Suppliers include Kitagawa, M M , and Scott/Davis. (I or 2,5,6). As presunqtve test, use method for aliphatic alcohols (see BUTYL ALCOHOL). U 3,6). ------- METHYL ACETATE l-L 3 CCOOCH 3 Syncrnyms: None common. Description.: Colorless, flarmnable, volatile liquid; fragrant odor. Floats; miscible with water. Toricity Local - May irritate respiratory tract. Systemic - Low; may be narcotic in high concentrations. Aquatic - (Low). Detection: Commercial kits are available; sensitivity range is 100- 3000 ppm. Suppliers include Scott/ Davis and Ritagawa. (1 5,6). ------- METHYL ACRYLATE H 2 C:CHCOOCH 3 Synonyms: Acrylic acid methyl ester, methyl propenoate. Description: Colorless, volatile liquid. Acrid odor. Floats, partially soluble. Polymerizes easily on standing: polymerization is accelerated by beat, light, and peroxides. The monomer is often inhibited by such substances as HYDROQUINONE. The polymer is a transparent, elastic, odorless, insoluble solid; it floats. The polymer is not toxic. Toxicity: (Monomer only) Local - Strong irritant and lacrimator. Systemic - Low; central nervous system effects from inhaling high concentrations of vapor. Aquatic - (Low). Other - As the monomer polymerizes, it may coat floating plants, shore structures, and exposed beach areas. RESPIRATOR AND PROTECT IVE CLOTHING ADVISABLE. Detection: Use gross presumptive test for unsaturation; see BENZENE for method. (1, 3). Specific identification requires hydrolysis and GC. ------- METHYLAMINE H 3 C NH 2 Synonyms: Arninomethane, monomethylainine. Description: Colorless flammable gas that may liquefy on very cold days (20°F). Marketed in liquid form or as a 33% aqueous solution. Strong odor of ammonia. Floats; very soluble. A strong base. The hydrochloride and picrate derivatives are soluble solids. toxicity: Lccal - Strong irritant. Systemic - Moderate by inhalation; low by other routes. Aquatic - High. Detection: Commercial kits are available; sensitivity range is 10-500 ppm. One supplier is MSA. (1,5,6). May also be detected by test for primary amine; see PROPYLAMINE for method. ------- METHYL SlIDE H 3 CN 3 Synonyms: None. Descripfiorn Colorless liquid that gasifies at room temperature. Reacts with water to form METHYL AMINE and nitrogen. Explosive. Totcity See METHYL AMINE. Detection See METHYL AMiNE. ------- METNYLETHYL PYRIDINE (H 3 C)C 5 H 3 N(C 2 0 5 ) Synonyms: Aidehyde coUidine, aldehycbne, ethyl picoline, MEP. Description: Colorless liquid with sharp, biting odor. Floats; slightly soluble. Combustible. The hydrochloride and picrate derivatives are soluble solids; the hydrochloride is colorless, the picrate orange. Toxicity: See PYRIDINE. Detection: Test for secondary amine as follows. Prepare reagent by dissolving 0. 5 g NiC1 1 he.xahydrate in 100 ml water. While shaking, add CS to slight excess. Just before testing sample, add 2 ml concentrated N}1 4 0H to 5 ml of reagent. Then add sample. Positive result; well- defined precipitate. (1,3). Specific identification may be accomplished in an improvised laboratory equipped with a UV spectrophotometer. ------- METHYLISOBUTYL KETONE (CH 3 )zCHCH 2 COC H 3 Synonyms: Hexone, i sopropylac etone, rnethylpentanone, MIB1c. Description: Co]nrless, stable, flammable liquid. Pleasant odor similar to camphor. Floats; slightly soluble. Toxicitr Local - Irritant. Systemic - Moderate to high. Some States restrict the use of MIEX because of its toxicity. Aquatic - (Moderate). N. B. Many authorities give this compound much lower ratings; the ratings given here are pessimistic and conservative. Detection: Commercial kits are available; sensitivity range is 5-1000 ppm. Suppliers include Scott/Davis and Ritagawa. l, 5,6). ------- METHYLMETHACRyLATE Synonym: Acrylic resin monomer. Description: Colorless, clear, volatile, flammable liquid. Sharp, fragrant odor. Floats; slightly soluble. Readily polymerized by light, heat, ionizing radiation, and catalysts. The monomer is usually shipped with a polymerization inhibitor (such as HYDROQUrNONE ). Toxicity; Local - Very irritant. Systemic - Moderate. Aquatic - Moderate. RESPIRATOR AND PROTECTIVE CLOTHING ADVISABLE. Detection: Specific identification requires hydrolysis and GC. As presumptive test, use method for detecting unsaturation (see BENZENE for details). ------- MOLASSES Mixed sugars Synonyms: Blackstrap. Description: The dark, syrup liquid residue after sucrose has been removed from the juice of sugar beet or cane. Composition varies with the extent of sugar removal. Blacketrap molasses (from which no more sugar can be economically removed) contains about S0% sugars, 20% other organics, 10% ash 1 and 20% water. Sinks and dissolves. Viscosity depends on temperature. Toxicity: Human and Aquatic - Practically nontoxic. Other - Raises BOO; may smother bottom life; may taint the flavor of fish and foul surfaces. Detection: Treat as mixed sugars. For recommended methods, see GLUCOSE and FRUCTOSE. ------- MOLYBDIG ANHYDRIDE MoO 3 Synonyms: Molybdenum trioxide, molybdic oxide or acid anbydricle. Description: White powder or granules which may be tinged with yellow. Siüks; very sparingly soluble. Toxicity: Human - Low. Aquatic - Moderate. More toxic in hard than in soft water. Detection: Dissolve suspect solids in 3M HCL Test filtrate and suspect liquids as follows. Dissolve 0. 5 g NZH4:Hz50 4 in 2 ml of sample in a test tube. Add 4 ml aqueous methylene blue. Place the test tube in boiling wat er. Positive result: the methylene blue is decolorized. lttrates and thiosulfates interfere. (1 .4,6). ------- MONOETI4ANOLALMINE HO(CH 2 ) 2 NH 2 Synonyms Ethanojarn.ine . MEA, calamine, aminoethanol, hydroryethylarnine. Descriplioxu Colorless, rather viscous, hygroscopic liquid. Amrnoniacal odor. A strong base. Miscible with water. Sinks in clean fresh water; may float on heavily polluted or salt or brackish water. Corn- bustible. Absorbs CO 2 and 142$. Toxicity: Local - Irritant, especially to the eyes. Systemic - Low. Aquatic - Moderate. Detection: Mix 3 ml of sample with 3 ml of 15% sulfuric acid. Acid to it 2 ml of 3% periodic acid. After 2 minutes, dilute with 5 ml of water. Then test for FOItMALDE- HYDE and AMMONIIJM (see FORMALDEHYDE and AMMONiA for details of methods). (1, 5). Alternatively, test for primary amine; see PRC)PYLAMINE for details of method. (I, 3J. The odor of ammonia and the pH may be sufficient for detecting significant concentrations. (1, 3). ------- MONOLSOPROPANQLAJ4j q H 3 CCH (OH)CHzNH 2 Synonyms: Anñnopropanol, hydroxypropylarnirte, MIPA. Description: Clear, colorless liquid. Slight ammoniacal odor. Floats and dissolves. Combustible. Toxicity: See MONOETHANOLAMINE. Detection: See MONOETHANOLAMINfl ------- MUSTARD GAS (C1CH 2 CH 2 ) 2 S Synonyms: Bis(cIdoroethyl)suI flde dichioroethyl sulfide. dicblorodiethyl sulfide, Hi). sulfur mustard. Descri0fl Oily liquid. A strong blistering agent, used as a war gas. Weak, sweet odor. Forms prisms at 55°F. Sinks; sparingly soluble. Decomposed by water. Toxicity: Local - Powerful vesicant Burns. blisters and quickly causes conjunctivitis and blindness. Violently corrosive to all tissues. Systemic - Thghly toxic by all routes, incluaAing skin penetration and inhalation. Aquatic - gL WEAR RESPIRATOR AND FULL PROTECTIVE CLOTHING. DetecUon Several types of papers, kits. tubes, and crayons for detection are available from the U. S. Army Chemical Corps. (2,5,6). Because mustard gas is decomposed by water, it is possible to test samples for sulfide, using the metltd given for AMMONIUM SULFIDE. (1,4). ------- QIPHTHALENE C 10 H 8 , bicycic 1 mnyms: Naphthene, napthalin, tar camphor. scription White, crystalline, volatile flakes (a common variety of moth flakes, moth balls, etc.). Strong odor of coal tar. Sinks; practically insoluble. Combustible. nicity: Local - May irritate skin. Systemic - Low. Aquatic - High. )decion: Use presumptive test for unsaturation; see BENZENE for details. For speciüc identification, extract the sample with ether, then use liv. ------- NAPHTHALIC ACID C 10 H 6 (COOH) 2 , bicyclic Synonym: Naphthalene thcarborylic acid. Description: White crystals that sink in water; practically insoluble. Toxicity: Human - (Low). Aquatic - Moderate to high. Detection2 See NAPHTHALENE and BENZ ENE. ------- MP}ITHENIC ACID C 6 H 10 COOH arid similar structures. Istlodes: A group of saturated cycloalkyl fatty acids, especially cyclohenneca rboxylic acid (hexahydrobensoic acid . Description; The commercial grade is usually a mixture of acids; dark, foul-smeUing, corrosive (to metals) solids and sludges. Usually sink (depends on commercial grade and density of the water); slightly soluble. Pure cyclohexanecarboxylic acid is a colorless solid, which may be odorless or slightly smelling of valerian (very unpleasant): it may sink or float, and is slightly soluble. tancity: Human - Low. Aquatic - Moderate to high. )mection: There is no suitable method for detection at water’s edge. In an improvised laboratory, potentiometric titration and CC may help idenlifica- tion. ------- NAPHTW)L C 10 H 7 0H. bicycic Synonym: liydroxnapl’ &ene. Descriptiorn Shiny wbite pouder or bulky leaflets which darken on exposure to sunligM and with age. Faint odor of phmxL Con*uslible. Sinks; slightly sol.hle. Toxicity: Local - May produce pe l 4 ng and discoloration of skin.. Systemic - Low. Aquatic - ltgh. Other - Small emounts taint the flavor of fish. Detection; Can tnt for unsaturatlon (see BENZENE) or for aromatic alcohol, as follows. Combine 2 ml of sample with 5 nil of reagent (a 10% solution of ceric ammoni nitrate in ZN uitric sad). Positive result greenish bnwn to precipitate. (1 . 3). To detect the beta isomer, mix 1 nil of the sample with S ml of 0.1% malic acid in concentrated sulfuric acid. Positive result the beta isomer gives a yellow solution that fluoresces blue. (1, 5). To detect the alpha isomer 1 mix 2 nig of acsinilide with 1 nil of 10% sodium nitrite and I ml of concentrated HCL After letting stand for 1 minute, add 1 ml of 1014 NaCH and 10 mg of urea. Thai add Z ml of eth,vwiil and I ml of sample. Positive result the alpha isomer turns the solution red or orange. (1 5). ------- *APHTHYLAMINE C 10 H 7 NH 2 , bicyclic Synonyms: Aminonaphthalene, naphthalidine. liclodes: Both the alpha and beta isomers and their common derivatives. Description: White to reddish crystalline solid which reddens on exposure to air and light. Sinks, but may float in polluted, salt, or brackish water. Slightly soluble. The HCl derivative is quite soluble, and the acetate derivative is very soluble. AU the derivatives are sensitive to light and expOsure. Tox icity : Human - A KNOWN CARCINOGEN, outlawed in at least one State. Acute toxicity is moderate. Aquatic - (Moderate). YEAR FULL PROTECTWE CLOTHING; RESPIRATOR ADVISABLE. Ddection: Several methods are available. (I). Naplithylamine reduces warm axnrnoniacal silver nitrate solution. Positive result: precipitate. (1, 5). (U). Extract samples with chloroform and separate. Irradiate the chloroform extract under a UV lamp for 10 minutes. Positive result: the extract turns red or orange. (1,5). (UI). Test for primary amine; see PROPYLAMINE for details of method. (1,3). ------- NEUTRAL SURFACTAI4TS RSO Na Includes: A wide variety of neutral detergents, all the sodium salts of sulfated fatty alcohols derived from various plant and animal sources. Two of the most important are sodium lauryl sulfate (although the article of conirnerce is a mixture of alkyi sulfates, with the laur ate predominating) and u-octyi sodium sulfate (the so- cafled Gardinol family of detergents). Some of the most im- portant brand names are Gardinol. Duponol, Modinal, Aurofix, Moprofix, Tergavon, Sandopan, Cyclopan, Cyclanon, Sapidan, Lissapol, Teepol, and Irium. Description; White or cream colored crystals, flakes, and powders. Faint fatty odor. Smooth feel. Neutral to litmus. Sink and dissolve readily, giving an opalescent soapy solution. These common wetting agents and detergents are widely used as ingredients of tootlipastes, cosmetics, etc. Toxicity: Human- Low. Aquatic - Reports vary; sometimes High, usnafly Low. Other - Can cause extensive foaming and sudsing. Detection: Mix sample with 10 ml of chloroform and 20 ml of axnmonium hezathiocobaltate reagent (200 mg ammoniumn thiocyanate and 30 g Co(N0 3 ) 3 in one liter of water). Positive result: blue chloroform layer. (1, 4). ------- NICKEL AMMONIUM SULFATE NiSO 4 - (NH 4 ) 2 50 4 Synonyms: Ammo nium ü ckel sulfate, ammo ni urn dis ulfatonickelate. Description: Bluish -green crystalline solid that sinks and dissolves. Concentrated solutions are slightly acidic. tori city: Local . Irritant to skin. Systemic - Low but may be carcinogenic. Aquatic - High. N. B. Nickel compounds are highly toxic to fish and zooplankton. Soluble nickel compounds spilled in water may be precipitated by such natural phenomena as absorption of CO 2 . hydroxylation, and reactions with sulfides. Collect suspect solids and bottom samples and boil them with HNO 3 to redissolve the nickel, which may then be detected by the methods given below. Detection: Test for the Ni, NH 4 , and SO 4 components separately. Test for nickel as follows. Drop concentrated NH 4 OH into 2 nil of sample until the solution is basic. Filter if a precipitate forms. Add 1 ml alcoholic saturated dimethylglyoxime to the filtrate. Positive result: a pink or red precipitate. Ferrous, cupric, and cobaltous ions interfere. (1, 4). See AMMONIUM ACETATE for tests. See ALUMINUM SULFATE for 504 tests. ------- NICKEL CHLORIDE NiC 1 2 Synonym: Nick elous chloride. Description: Golden powder, brown scales, or green crystals, depending on degree of hydration and technical purity. All forms are deliquescent. Sinks and dissolves. The aqueous solution is mildly acidic (pH of 4). Toxicity: Human - Low. Aquatic - High. Detection: See NICKEL AMMONIUM SULFATE for Ni methods. See AMMONIUM CHLORIDE for Cl methods. ------- NICKEL NITRATE Ni(N0 3 ) 2 Synonym: Nickelous nitrate. Description: Green, deliquescent crystals that sink and. dissolve, giving a mildly acidic solution (pH of 4). A strong oxidizing agent.. Toxicity: Local - Irritant. Systemic - Low. Aquatic - High. Other - Even if the Ni should be precipitated from solution, the NO 3 may stimulate plant growth. Detection: See NICKEL AMMONIUM SULFATE for Ni methods. See AMMONIUM NITRATE for NO 3 methods. ------- NICKEL SULFATE N ISO 4 Synonym: Nickelous sulfate. Description: Crystalline solid, which may be yellowish bluish, or clear green, depending on degree of hydration. Sinks and dissolves. The solution has a sweet, astringent taste. The solution is mildly acidic (pH of 4. 5). Toxicity: Local - Irritant. Systemic - Low. Aquatic - High. Detection: See NICKEL AMMONIUM NITRATE for Ni methods. See ALUMINUM SULFATE for 504 methods. ------- NITRIC ACID I- 1N0 3 Synonyms: Aqua fortis, azotic acid, engraver’s acid; ingredient of mixed acid, nitrating acid, aqua r egia, niitrohydro chioric acid, nitrornuriatic acid, chloronitrous acid, chioroazotic acid. Description: CLear to light-brown liquid; may he yellowish and fuming. Suffocating odor; caustic and corrosive. Decomposes in strong light and heat, turning reddish. A very strong oxidizing agent, and one of the strongest acids. Extremely reactive. toxicity: Local -. The liquid causes severe burns. The vapor is strongly irritant, and may cause fatal lung injury. Systemic - Moderate to high. Aquatic - Moderate to high. Other - Corrosive to nearly everything it touches; look for extensive corrosion damage. Nitrates are plant nutrients; look for growth stimulation of plants downstream. WEPSR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Test first with pH indicator or meter for an acid (1, 3, possibly 6). Then test for NO 3 ion; see AMMONIUM NITRATE for method. ------- NITRIC OXIDE MO Synonyms: Mononitrogen monoxide, nitrogen monoxide. Description: Colortese gas or liquefied gas. Immediately on contact with air, NO It converted into the highly toxic brown NITROGEN DIOXIDE, NITROGEN TETRO]CIDE, or both. Turns brown in air. The gas and its oxidation products are soluble in water, giving NITRIC ACiD and related acids. Toxicity: See NITROGEN DIOXIDE and NITRIC ACID. Look for corrosion effects. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detectiorn Commercial kits are available for detecting NO; sensitivity range is 0. 5-1000 ppm. Z, 5,6). Also see NITRIC ACID. pit is a good indicator of aquatic hazard. ------- NITR.OAN ILINE H 2 NC 6 H 4 NO 2 Synonym: Nitrani.line. Descriptiorn Yellow to orange crystalline solid. Discolor. in strong light. Sinks; slightly soluble. Toxicity: Local - lrrttant. Systemic - Moderate to high by all routes, including inhalation and absorption through intact skin. Aquatic - Moderate. EAR RESPIRATOR AND PROTECTWE CLOTHING. Detection: Speci c identification of the isomers can be accomplished by UV spectros copy. (1, 516). Gross presumptive tests include unsaturation (see BENZ ENE for method) and primary amine (see PROPYLAMINE for method). ------- NITROBENZENE C 6 11 5 NO 2 Synonyms: Nitrobenzol, oil of mirbane. Description: Colorless to pale yellow oily liquid; freezes at 43°F to give yellow crystals. Odor of almonds. Sinks; slightly soluble. Forms an explosive vapor layer above the water surface. Toxicity: Local - Irritant, especially to the eyes. Systemic - Moderate by a U routes, including inhalation and absorption through intact skin. Aquatic - High. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Extract 10 ml of sample with 5 ml of ether and evaporate the ether on a steam bath. Carefully add 3 ml of concentrated to the residue. Positive result: solution turns yellow. Nitrotoluene (which is also a toxic industrial material) interferes. (1, 5). ------- XITROCHLOROBENZENE CIC 6 H 4 NO 2 Synonym: Chlorothtrobenzene. Description: Combustible yellow crystalline solid. Sinks; Virtually insoluble. To xicity: Local - Irritant. Systemic - Moderate. Aquatic - High to moderate. PROTECTIVE C LC) THING ADVISABLE. Detection: The only suitable test for use at water’s edge is the presumptive test for unsaturation (see BENZENE for method). In an improvised labora- tory, use GC for identification. ------- NITROCRESOL Synonym: MethylthtrOpheflOL Description: Yellow, combustible, crystal l ine solid. Sinks; slightly soluble. Toxicity: Human - Moderate to high by all routes. AqusUc - (Moderatal. flOflCTWE CLOTHING ADViSABLE. Daect in For gross pr.s qtn mdbod. test for unsaturation (see 5F31Z721E for method . In an improvised laboratory, U n UT .pectrvscOpy. ------- MTROGEN DIOXIDE wnyms: None common. Dsscription Reddish brown gas, liquid below 7 2°F. Suffocating sharp odor. The commercial brown liquid under pressure is often called “nitrogen tetroride” or “N-two-O-four” although in actuality it is an equilibrium mixture of NO and the colorless P1204. The liquid sinks and dissolves . forming NITRIC ACID and NITRIC OXIDE. The gas dissolves, forming the same products. The gas is an insidious deadly poison. Inicity: See NITRIC ACID. YEAR RESPIRATOR AND PROTECTIVE CLOTHING. Ddecfion Commercial kits are available; sensitivity range is 0.1-1000 ppm. Suppliers include Davis, Kitagawa, MSA, and Scott/ flats. (2, 5,6). ------- NITROGEN TETROXIDE N 2 0 4 Synonyms: None common. Descriptiorn This colorless gas is very unstable, and spontaneously decomposes into NITROGEN DIOXIDE. Totcity See NITROGEN DIOXIDE and NITRIC ACiD. DetectiOn2 See NITROGEN DIOXIDE and NITRIC ACID. ------- JITROPHENOL } 5OC 6 H 4 N0 1 Spsnyrns: None common. De.cription: Yellow crystals that sink in water; slightly soluble. A widely used p1-i indicator for acids. Depending on the isomer, the indicator solution turns from colorless in strong acids to bright yellow in weak acids. T thcity: 1 -lurnan - Moderate to high. Aquatic - Moderate. Mection: Only the grossest presumptive test is suitable for use at water’s edge; perform test for unsatura- tion (see BENZENE for method), in an improvised laboratory, use UV spectroscopy. For another presumptive test, see comments above under “Description”; this test is based on n.itropbenol as a pH indicator, but the color change is not sharp and CO 2 interferes. ------- NITROPROPANE C 3 Synonymst None commOn. Descriptiorn Colorless, flanwnsble liquid. May float or sink depending on the dissolved solids in water. Slightly soluble. Toxicity: Hnnian - I 4 ow . Mualic - (law). Detection Commercial kits are available; sensitivity range is 5-150 ppnz. One supplier is MSA. (1, 5,6). ------- ifROUS ACID uonyms: None common. scriptioni A weak acid, known only in solution, which is pale blue. Changes rapidly in water to NITRIC OXIDE and NITRIC ACID. Forms stable, soluble nitrites with several common cations, including Na, K, and Ca. lthcity: Similar to NITRIC ACID, but lower. Nitrous acid is a known mutagen, and may produce genetic effects. Mection: See NITRIC OXIDE and NITRIC ACID. Commercial kits for nitrite or nitrate/nitrite detection are available from Lamotte, Taylor, HeUige , and Hach. Sensitivity range is 0.1 - 1200 ppm. (2,5,6). ------- NITROUS OXIDE N 2 0 Synonyms: Dinitrogen monoxide, factitious a, hyponitro us anhydride, laughing gas. Description: Colorless asphyxiant gas. Slightly sweet taste and odor. Soluble. Supports combustion, but stable and inert at room temperature. Commercial form is liquefied gas. toxicity: Human. Low. Aquatic - (Law). Other - The water solution of nitrous oxide is a mildly corrosive acid. Detection: Commercial kits are available; sensitivity range is 0. 5-1000 ppm. One supplier is Scott/Dav is. (2,5,6). ------- ROXYLOL (CH 3 ) 2 C 6 H 3 N0 2 5monyxn: Nitroxylene. )scription: Yellow liquid or yeUowish crystalline solid, depending on the isomeric form. SinXs; practically insoluble. Taxicity: Local - I rritant. Systemic - Moderate to high. Aquatic - (Moderate to high). section: At water’s edge, even the gross presumptive test for unsaturation (8ee BENZENE for method) may fail. In an improvised laboratory, use GG. ------- OCTYL ALCOIKIL C 8 H 15 0H Synonyms: Octanol, heptyl carbinol . capryl alcohol, methylberyl carbinoL. Descripticxn There are 2 common isomers, which have somewhat different properties. The x i isomer is a coiorless com- bustible liquid with a penetrating aromatic odor. Floats: very insoluble. The sec isomer is a colorless, refractive, combustible, oily liquid which floats and is slightly soluble. Its odor is much less pronounced. Both isomers are used as antlfoaming agents. Ton cit y : Human - Low. Mnfic - Moderate. Detecfion Test for sliphatic alcohol (see BUTYL ALCOHOL for method). In an improvised laboratory. use OC for identificabon. ------- CLEIC A c m H 3 C(C 1 1 2 ) 7 C 1 1:CH(CH 3 ) 7 COOH Synonyms: Octadecenoic acid, Turkey red oil. ]Description This acid is a component of all natural fats and some oils. Commercial grades are yellow to red oily liquids that darken on exposure to air and solidify at about 40°F. SmeU like lard. Combustible. Floats; practically insoluble. Purified grades are nearly color- less and odorless; they are used in making soft soaps and oil solvents. Toxicity: Human - Low. Aquatic - (Low; but there have been reports of high fish toxicity from sodium oleate.) Detection: Use presumptive teat for unsaturation (see BENZENE for method). For more precise identification, extract the sample with ether, evaporate the ether, then deter- mine the iodine value of the residue or use GC; these methods are more suitable to an improvised laboratory than to a test at water’s edge. ------- OXALIC AC m HOOCCOOB Synonyrn Etbanedioic acid. Description: Transparent, colorless crystals. Sinks and dissolves. Acid to litmus. Corrosive. Toxicity: Local - Strongly irritant. Systemic - Moderate. Aquatic - Moderate. WEAR PROTECTIVE CLOTHING. Detection: Use pH indicator for strong acid (1, 3). Then mix 1 ml of sample with I ml of 1:9 sulfuric acid. Add slowly and carefully S mg of metallic zinc. Let stand for 30 minutes. Add slowly 2 r i -il of 0.01% 2, 7-dibydroxynapbthalene in 1:1 sulfuric acid. Heat in boiling water for 5 minutes. Posi- tive result: solution turns red. (1, 5, 6). ------- OXYPROP IONIflLLE O(CH 2 CH 2 CN) 2 Synonym: ODPN. Description: Colorless, coinbustile liquid that sinks and dissolves. Toxicity: Human - Low. Aquatic - Low. Detection: There is no suitable method for detection at water’s edge. In an improvised laboratory, use GC. ------- PARAFO IU&&LDZHYDE ROICHaO)nM Synonynt Paraform.. Includes: 3 y -frionne. PABAFORMALDEHYDE is a polymer of VORMALDEHYDE in which n is 8-100: in this listing we Include all polymeric forms of PORI4ALDEHYDE. D..criptiorn PARAFORMALDEHYDE is a white solid with a slight odor of Formaldehyde. Cornmercisfly available as flakes or powders, used in germicides. SUik., but soinbility depends on the else of the polymer: lower polymers are much more soluble than higher polymers. Cmnbostible. !x!! .trtonne is awbite crystatlint soli d with a pronounced foewnaldehyde odor; it sink. and dissolves. Toxicity: Systemic - Moderate. Aquatic - Moderat, to low, depentlifl on actability. D dot (I). [ )dMct as FORMALDEHYDE (see that entry for method). (U . Alternatively apply a g eral teat for aliieh rdes, as follows. Add 2 ml of Baudict’s solution to S ml of sample. Betedicts solution is made as follows. Combine 17.3 g of h rdnted cupric sulfate, 173.0 g of sodium citrate, and 100 g of anhydroos sothum carbonate: add distilled water to r ake I liter. Positive result el i aldehydes give a yellow to green precipitate. (1. 4). (1113. Alternatively, apply the following test for aldehydee. Mix 2 ml of sample with 2 ml of dilute sulfurous acid and I ml of 0.1% fuchein in sulfurous acid. Positive result solution turns violet or blue. (14). ------- PENTANAL H 3 C(CH 2 ) 3 CHO or (H 3 C)ZCHCHZCHO Synonyms: A my! aldehyde. isovaleral, isovaleraldebyde isovaleric aldehyde methylbutyraldehyde valeral valeraldehyde nleric aldehyde. Description: Clear colorless flammable liquid. floats; slightly soluble. Isovaleral.dehyde has & strong smell similar to apples.. Toxicity: Human - Low. Aquatic - Low. Detection: Detect as aldehyde; see PARAFORMALDEHYDE for Tfl etbods. ------- PENTANE C 5 H Synonyin Amyl hydride. Description: Colorless, flammable liquid. Pleasant odor. floats; soluble. Used in pesticides. Toxicitr Human - Slight. Aquatic - Moderate. Detectiorn Commercial kits are available for detecting hydrocarbons. Scott/Davis is one supplier. (1 ,4,6). ------- PENTANOL C 5 H , OH Synonyms: Antyl alcohol, methyl propyl carbinol, methylbutyl alcohol, ethyipropanol, di ethyl carbinol, methylbutanol, dimethyl ethyl carbinol, amylene hydrate. Includes: 1usd, which is a mixture of alcohols, largely pentanols. Description: The various isomers of pentanol have somewhat different properties. All are colorless, flammable. volatile liquids that float on water. All are flotation agents. The tert isomer smells like camphor; other iscmeru nave a mild udor. Depending on the isomer, pentanol is slightly to very soluble. Fusel oil is an oily, volatile liquid that floats and is slightly soluble. Toxicity: Human - Low to moderate, depending on isomer. Aquatic - Moderate. Detection: Detect as aliphatic alcohol; see B1JTYL ALCOHOL for method. ------- PENTENE Sywnyxns: Amylene, propylettylene, niethylahylethylene. Descriptiorn There are several isomers. Flammable, clear liquids. float; practically insoluble. trans - Z- peatene is a polymerisatlon inhibitor, aS may be mixed with active mo mers (e.g. ,. acrylates). Tori citr _- Pa ). _ _ _ _ - Moderate to high. Daectloa Test br unsaturation; see BENZENE for method. ------- PHENOL C 6 H 5 OH Synonyms: Carbolic acid, cresylic acid, hydroxybenzene, phethc or phenylic acid. scripfion: Colorless to pink crystalline solid or fluid. Reddens on expos are to air. Characteristic odor and taste of disinfectants. Sinks and dissolves readily. aricity: Local - Irritant, caustic to skin. Systemic - Moderate to high by ingestion. Aquatic - High for almost all forms of aquatic life. Other - Subtoxic amounts may taint the flavor of fish. TEAR PROTECTWE CLOTHING. )etection: Commercial kits are available; sensitivity range is 0. 5-10 ppm. One supplier is Scott/ Davis. (2, 5,6). ------- PHENYLCARBYLAMD E CHLORIDE C 6 H 5 NC C l 2 Synonyms: None common. Descriptioir A chemical warfare agent. Pale yellow oil v liquid. Mildly volatile; odor like onions. Sinks; practically insoluble. Toxicity: Local - Extremely irritating to skin and mucous membranes. Systemic - High. Aquatic - (High). WtAR IU PIBATOR AND PROTECTLVE CLOTI-ILNO. Detection: Kits are available from the U. S. Army Chemical Corps. ------- PHOSGENE 0CC ! 2 Synonyms: Carbon oxychloride, carbonyl chloride, chloroformyt chloride. Description: Colorless gas that condenses at about 32°F to a clear, colorless, fuming liquid. Suffocating odor; in great dilution with air, smells like moldy hay. Sinks; slightly soluble in water 1 and slowly hydrolyzed to yield, CO and HYDROCHLORIC ACID. Used in chemical synthesis and in chemical warfare. Toxicity: Local — Insidious irritant, especially to respiratory tract. Systemic - 111gb, especially by inha 1 ation. Aquatic - (High). WEAR RESPIRATOR AND PROTECTIVE CLOTHiNG. Ddection: Several commercial kits are available; sensitivity range is 0.1-15 p n. Suppliers include M M, Kitagawa, and Scott/ Davfs (Z, 5,6). Alternatively, the following method may be used. Paper soaked in an alcoholic or carbon tetracbloric solution containing 101?. of a tniture of equal parts of p-dirnethylaznino- benzaiAehyde and colorless diphenylamine. then dried, will turn from yellow to deep orange in the presence of the maximum allowable concentration of phosgene. (2,5 ,6 ). ------- PHOSPHORIC ACID HPO and (HPC 3 4 3x Synonyms: None corrirnon. Includes: The meta and ortho isomers. Description: Theo isomer is a clear, colorless, sparkling, syrupy liquid or transparent crystalline solid, depending on concentration and temperature. Pleasing acid taste in dilution (111cc soda water). Sinks; miscible with water. The rn isomer is a glassy, transparent, detiquescent mass. It sinks and dissolves easily. The rn isomer slowly con- verts to theo form. Both isomers are cQrrosivc to ferrous metals and alloys; both are acid to litmus. Toxicity; Local - Concentrated solutions (75%) are irritant. Systemic - Low. Aquatic - High. Detectiorn Test first with pH indicator for acid. Then test for phosphate ion; see AMMONIUM PHOSPHATE for method. ------- PHOSPHORUS p Synonyms: None common. Includes: White, black, and red forms. Description: White (or yellow) phosphorus is a crystalline, waxy, volatile, transparent solid. Darkens on exposure to light. It glows in the dark. Risk of fire and explosion. Sinks; insoluble. Red phosphorus is a red to violet powder. Much less reactive than the white form. Sinks; insoluble. toxicity: N. 13. The following ratings are for white phosphorus; the red and black forms are practically non- toxic except when they contain the white form as an imparity. Local - Severe burns and irritation. Systemic - Moderate to high: corrosive and toxic. Aquatic - High. Detection: 1.. White phosphorus. Keep under water and handle only with forceps. Add iN nitric acid to the sample, which converts it to PHOSPHORIC ACID. See PHOSPHORIC ACID and AMMONIUM PHOSPHATE. 2. Red or black phosphorus. Add 3N nitric acid to the sample; which converts it to PHOSPHORIC ACID. See PHOSPHOR iC ACID and AMMON1UM PHOSPHATE. ------- PHOSPHORUS OXYGHLORIDZ PO d 3 and P 1 0 3 C 1 4 Synonyin Phosphoryl chloride. Dacriptiorn Colorless, (mT.ng liquid; biting odor. Sinks; decompose. on contact with water to HYDROCHLORIC Acm . d niospwonc ACID. Totcity: Local - remely irritatng and caculic. Severe respiratory damage. Systenic and Muatic - See HYDROCHLORIC ACID and PHOSPHORIC ACID. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detectiorn See HYDROCHLORIC ACID and PHOSPHORIC ACID and AMMONIUM PHOSPHATE. ------- PHOSPHORUS PENTASULFIDE p 2 S 5 Sponyms: Phosphoric sulfide, phosphorus persulfide , thiophosphoric anhydride. Dscriplion Light yellow or greenish crystalline masses. Very hygroscopic. Peculiar odor similar to HzS. tgnites and burns by friction. Decomposed by moist air and water to form H 2 S and PHOSPHORIC ACID. Used in manufacture of matches and ignitIon compounds. Toxicity: Local - Strong irritant. Systemic - (Moderate). Aquatic - High. Detection: Detect as PHOSPHORIC ACID and sulfide (see AMMONIUM SULFIDE). ------- PHOSPHORUS TRICHLORIDE PC i 3 Synonym: Phosphorus chloride. Description: Clear, colorless, fuming liquid. Decomposes rapidly in moist air and water to form HYDROCHLORIC AC m and phosphorous acid. Sinks and decomposes. Toxicity: Local - Intensely irritant and corrosive. Systemic and Aquatic - See PHOSPHORIC ACID and HYDROCHLORIC ACID. RESPIRATOR AND PROTECTIVE CLOT RING ADVISABLE Detection: See PHOSPHORIC ACID and HYDROCHLORIC ACID. Although the ultimate hydrolytic and oxidation products of PC1 3 are HYDROCHLORIC and PHOSPHORIC ACIDS, phosphorous acid is formed first, then slowly oxidized to H 3 P0 4 . To detect phosphorous acid, add to the sample 0. IN iodine a little at a time. Positive result: the iodine solution is decolorized. (1, 4). Many sub— stances interfere. ------- ICLYGLYCOL ETHER Synonynt Polyether glycol. Description: A large family of polyalkyl glycols, including mono- and dialkyl ethers of all types. They are largely clear colorless liquids, often hygroscopic, and dissolve reathly in water. They are common solvents and antifeezes of low toxicity. They often have a pleasant aromatic or fruity odor and a slightly sweet taste. They are important in water polluthon primarily because of the large oxygen demand they make: a major BOO problem would result from any sizable spill. Yazicity: Human and Aquatic - Low. Other - Raises BOD. Ddection: Mix 10 nil of sample with 2 ml of h4 HCI and 2 ml of 10% Bad 2 solution. Add 2 ml of 10% phospbomolybciic acid. Let stand for 30 minutes. Positive result: green precipitate. (1,4,6). To be more specific, collect this precipitate, filter it, and wash it first with 3 ml of 1:100 UC1. then with 7 nil of water. Dissolve the precipitate in a mixture of 3 nil concentrated H 2 S0 4 , I ml concentrated HN0 3 , and I nil of 70% percliloric acid. Add 20 ml of water and 2 tnt of 40% NaCH solution.. Finally, add 5 nil of 5% phenyihydrazine in 1:20 H 2 S0 4 . Positive result: solution turns blue. (2,4,6). ------- POTASSIUM CHROM&TE K 2 CrO 4 Synonynu Neutral potassium chrornate. Description: Lemon yellow crystals. Sink and dissolve. Alkaline to litmus. Corrosive. Toxicity: Local - Strongly irritant. Systemic - High by ingestion. Muatic - High to moderate. Detection: See AMMONIUM CHROMATE for detecting Cr0 4 . The K ion is so comnn, background may be a severe detection problem. A simple method for detecting K is as follows. Mix 1 ml of sample with I nil of ethanol and 1 ml of reagent (0. 5 g of sodium cobaltinitrite in 3 ml of water). Positive result; yellow crystals form. ------- POTASSIUM CYANIDE KCN $ynonytns: Cyanide of potassium, cyanide of potash. Description: White, deliquescent, crystalline so lid wbich is gradually decomposed by moisture and CO 2 . Readily soluble, but decomposes in water and light to yield POTASSIUM HYDROXIDE and HYDROCYANIC ACID. Violently poisonous, and forms poisonous vapors from solution. Concentrated solutions are strongly alkaline. toricity: Local - Strong solutions are caustic to skin. System -ic - High. Can be absorbed through injured skin. Aquatic - High. YEAR RESPIRATOR AND PROTECTIVE CLOTHiNG. Detection! See POTASSiUM CHROMATE for detecting K. See BARIUM CYANIDE and HYDROCYANIC ACID for detecting CN. ------- POTASSIUM DICHEOMATE Synonyms: Potassium hicbroxnate, red potas slum chrotnate. Description: Bright scarlet crystals. Bitter metallic taste. Sinks and dissolves freely. Strong oxidizing agent: reacts strongly with organic materials. Corrosive. Concentrated solutions are acid to litmus. Toxicity: Local - Strong irritant and caustic. Systemic - Moderate; a corrosive poison. Aquatic - Variable; usually moderate, but may be very high or rather low. Detectiort See POTASSIUM CHROMATE for detecting K. See AMMONRIM CHROMATE for detecting chromate and dicbrornate ions. ------- POTASSIUM HYDROXIDE KOff Synonyms: Caustic potash, potash hydrate 1 lye. Description: Deliquescent, white solid. Absorbs water and COz from air. Sinks and dissolves easily. A very corrosive alkali. Strongly alkaline to litmus. totcity: Local - Very corroskve and irritating. Burns tissues. Systemic - A corrosive poison. Aquatic -. Moderate to high. TEAR PROTECTIVE CLOTHING. )etectIon: Test with pH indicator for strong base. fl, 5, possibly 6). Then test for K ion (see POTASSIUM CHROMATE for method). ------- POTASSIUM PERMANGANATE KMnO 4 Synonynt Chameleon mineral. Descripfion Dark purple crystals with metallic sheen. SweS, with astringent aftertaste. Sinks and dissolves, giving an intense, dark violet solution. A powerful oxiditing agent which reacts with organic materials. Widely used as a disinfectant and bleach. Totcitr Local - Irritant. Caustic in high concentrations. Systemic - Low. Muatic - High for fish and algae. Detectiow If sample is cloudy or muddy 1 filter it. If the filtrate is not pink or violet, pennanganate is not present in detectable quantity. If the solution is pink or purple, add several drops of sample to 3% solution of hydrogen peroxide in 1:10 I-ICl. Positive result: the purple color is bleached. ------- PROPANAL C 2 H 5 CHO Synonyms: Propionaldehyde, propyl aldeiiyde, propionic aldehyde. Description: Clear, colorless, very ftarnn-iable liquid. Suffocating odor, floats and dissolves. Totcitr Local - Irritant. Systemic - Moderate by inhalation, low by ingestion. Aquatic - (Moderate or low). Other - Raiees DOD. TEA.R RESPIRATOR. DSection: Detect as an aldehyde; see PARAFORMALDEHYDE for methods. ------- PROPANOIC ACID H 3 CCH 2 COOH Synonyms: Methylacetic acid, propionic acid. Descriptiorn Combustible, colorless, oily liquid. Sharp rancid odor. floats and dissolves. The calcium salt is a common food preservative. Toxicity: Local - Skin irritant. Systemic - Low. Aquatic - Moderate. Detection: There is no suitable method for detection at water’s edge. In an improvised laboratory use GC with hydrophobic column (e. g. 1 Teflon). ------- PROPANOIC ANHYDRIDE (CH 3 CHzCO)zO Synonyms ; M ethylac etic anhyd ride, propionic anhydride. Description: Combustible, colorless liquid. Sharp rancid odor. Floats or sinks depending on temperature and solids content of water. Dissolves, and is converted to PROPANOIC ACID. Tothcity: See PROPANOIC ACID. Detection: See PROPANOIC ACID. ------- PROPYL ALCO}KTh C 3 H 7 OH Synonyms: Propanat, isopropanol. isopropyl alcohol, diniethyl carbinol. Description: Colorless, flammable liquid, completely miscible with water. The it isomer smells like ETHYL ALCOHOL; the iso form has the character- istic smell of rubbing alcohol, of which it is the principal ingrediait. Toriaty: Local - Practically none; may be slightly irritating. Systemic - Low for the n isomer; moderate for the iso trin, Aquatic - Moderate. Detectioni Commercial Icits are available; sensitivity range is 100-1000 pp4ki . Suppliers include MSA and Scott/ Date. U,5.6). Aheniabvely. detect as an aliphatic alcohol; see BUTYL ALCOHOL for Tfletbod. ------- 1%OPYLAMINE C 3 EL 7 NH 2 Synonym: Aniinopropane. Descrijtion: Colorless 1 volatile, flammable, liquid. Amine odor. Floats and dissolves. Toxicity Local - Strongly irritant as liquid and vapor. Burns skin. Systemic - Moderate by all routes, especially inhalation. Aquatic - Moderate. Detection: Test as a primary amine, as follows. Mix 2 ml of sample with 5 ml of 0. IM benzenesulfonyl chloride in 10% aqueous NaOH. There should be no precipita- tion at this point; if a precipitate forms, filter it out. Acidify the filtrate with dilute MCI. Positive result: precipitate forms. (1 ,3). For specific identification (which cannot be accomplished at water’s edge), use GC with a hydrophobic column. ------- PROPYLENE GLYCOL H 3 CCH(OH )CH 2 OH Synonyms: Dihydroxypropane , propanediol , methylethylen e glycol, methyl glycol, trimethylene glycol. Description: Colorless viscous, stable, combustible, hygroscopic liquid. No taste or odor. Slowly sinks; may float on salt or brackish water. Very miscible. Toxicity: Human and Aquatic - Low. Other - Raises BOD. Detectiorn Mix S ml of sample with 2. 5 ml of 6. 6% sodium periodate in a test tube. Let stand for 20 minutes. Cool to 32°F, then add 1 ml of saturated KNO 3 solution. Then add 1 ml of saturated piperazine hydrate solution and 0. 5 ml of 4% sodium nitro- prusside. Positive result: solution turns blue. (1, 5, 6). ------- PROPYLENE OXIDE H 3 CCHCH 2 O Synonyms: Propene oxide, epoxypropane. Description: Clear, colorless flammable liquid. Smells like ether. Floats; fairly soluble. Toxicity: Local - May irritate. Systemic - Moderate to low. Aquatic - (Low ). Other - Raises BOD. Detection: Commercial kits are available; sensitivity range is 100-4000 ppm. Kitagawa is one supplier. (1, 5,6). ------- PYRm INE N(CH ) 4 CH Synonyms; None comnn. Descript on: Colorless to slightly yellow liquid. Sharp, disagreeable odor, burning taste. A weak base. floats; completely miscible. Toxicity: Local - Irritant. Systamc - Low. A quatic - Moderate. Detection: Commercial kits are available; sensitivity range is 2.-SO pgnn. One supplier is MSA. (1 or Z• 5,6). Alternatively 1 test for secondary amine as follows. Prepare reagent by dissolving 0. 5 g NiCl bexahydrate in 100 ml of water. While shaking, add cZ to slight excess. Just before testing sample, add 2 ml of con- centrated NH 4 OR to S ml of reagent. then 2 ml of sample. Positive result a well-defined precipitate. (1,3). ------- PYROCATECHOL C 6 H 4 (OH) 2 Sy nyrns: B enzenediol, c atechol, dihydroxybenz ene, py roc atechin. Description: Colorless crystals that turn brown in light and air, particularly when moist. Sinks and dissolves. Aqueous solutions quickly turn brown. Reduces arnmoniacal silver nitrate and Fehling’s solution; forms a definite compound with boric acid. Toxicity: Local - Irritant and caustic. Systemic - Moderate. Aquatic - High. DMecfion Simple tests include unsaturation (see BENZENE for method), and addition of dilute ferric chloride, which turns pyrocatechol solutions green. (1, 4). A more specific test: Mix 2 ml of sample with 2 ml of 1% osmium tetroxide and 2 ml of 0.4% sodium carbonate solution. Positive result: solution turns reddish violet. (1, 5). Gallic acid and pyrogallol interfere. ------- PYROGALLOL C 6 H 3 H) 3 Synonyms: Bensenetriol, pyrogallic trihydroxyb ens ene. DescHption Shiny white crystals that turn gray on exposure to air and light. Sinks and dissolves. The water solution darkens on exposure to air, quite rapidly If the solution is alkaline. Toxicity: Local - Irritant. Systemic - Moderate. Aquatic - High. Detection: Detect as GALLIC ACID (see that entry for method) or as PYROCATECHOL (osmium tetroxide rnethod . ------- flTERNARY AMMONIUM SALTS (R 1 )(R 2 }N(R 3 )(R 4 ) ibides: Cationic surfactants and detergents, beazalkonium detergents, quaternary amines, and a l lcyl aryl animonium halides. There are dozens of brand names. )rscription: A large family of commercially important detergents, surfactants, antiseptics, and fungicides. They include such typical substances as benza.lkonium chloride. Gen— era.fly colorless to yellowish amorphous solids; frequently commercially available in aqueous solution. Aromatic odor, very bitter taste. They sink and dissolve readily, and will probably make flowing water foam and suds. Alkaline to litmus. utcity: Local - Slightly irritating; can crack and dry skin. Avoid spattering into eyes. Systemic - Moderate by ingestion. Aquatic - Moderate. Other - Can cause extensive foaming and sudsing. )etectiorz: Mix 1 ml of sample with 10 ml of bromophenol blue reagent. This reagent consists of 7% of 0. ZN sodium acetate, 91% acetic acid, and 2% of 0. 1% ethanolic bromophenol blue solution. Positive result: mixture turns sky blue. (1, 4). ------- QUDI&CRINE MynRocHl.ORIDE C 23 H 30 C1N 3 0 - 2 MCI tricycic Synonyms: The most comn n trade name for this antimalarial compound is Atabrine; there are at least a dozen other trade names. Descriptiorn Bright yellow crystals that sink and dissolve in water, giving an atrernely fluorescent solution that is blUer to the taste and acid to litmus. Toxidtr Human - Low. A quatic - Ill g b . Detection: The brilliant fluoresca Ce of this compound is detectable under UY light in dilutions of several parts per million (1,4). May also be detected by tests for unsaturatlon (lee BENZENE), and tests for secondary ani4nss (see PYR1DINE). ------- QU 1NHYDRONE C 6 H 4 (OH) 2 C 6 H 4 O 2 Synonym: Green quirthydrone. Description: The addition product of HYDROQTJINONE and QUINONE. Green crystals with metallic sheen; reddish brown by transmitted light. Sinks; slightly soluble. Toxicity: Human - Moderate to high. Aquatic - High. Detection: Detect as QUINONE and HYDROQUINONE. ------- QUININE C 20 H 24 N 2 O 2 , tetracycic. includes: Quinithne and the common derivatives. Synonyms: Trade names of this compound and its common derivatives run to several dozen. Descriptioru The pure substance is a bulky white amorphous powder or crystalline alkaloid. Odorless, very bitter. Sinks; slightly soluble. The more soluble derivatives include: the acid sulfate, bydrohalides, methiodide, tartrate, gluconate, sulfate, acetyl- salicylate, arsenate, ascorbate, benzoate, bisulfate, dihydrohalide., lactate, ethyl sulfate, and hypo- phosphite. Quinine and its derivatives have a characteristic blue fluorescence in dilute sulfuric acid. Toxicity: i fuman - Low, except by ingestion (moderate). Aquatic - Moderate. Detection: The very bitter taste of quinine (familiar as quinine bitters and quinine tonic water) can be detected at a few ppm. (1, 5, 6). Alternatively, mix Z ml of sample with 1 ml of 2% eosin solution and 2 ml of 5:1 0. 2M disodiurn phosphate and 0. 1M citric acid. Positive result: solution turns red. (2, 5,6). ------- QUINOL iTNE C 9 H 7 N, bicyclic Synonyms: Benzazine, bentopyridine, chinoleine, leucoline. Description: Refractive, colorless, hygroscopic liquid that darkens with age, light, and moisture. Sharp odor. Like pyridine. Just sinks; may float on salt or brackish water. Slowly dissolves. toxicity: Human - Moderate. Aquatic - Moderate to high. Detection: Detect as secondary amine (see PYRIDINE) or as unsaturated organic (see B,ENZENE). In an improvised lakx,ratory, UV spectrophotometry is the preferred method of identification. ------- QUINONE C 6 1 1 4 0 2 Synonyms: Benzoquinone, chinone, cyclohexadienedione. Description: Yellow crystals. Penetrating odor like chlorine. Irritating vapors. Sinks; slightly soluble. Combustible. Toxicity: Local - Vapors and solutions are very irritating and can cause severe skin and eye damage. Systemic - Moderate. Aquatic - High. RESPIRATOR AND PROTECTIVE CLOTHING ADVISABLE. Detection: ktx 2 ml of sample with 2 ml of aqueous saturated rhodarnine solution and 2 ml of con- centrated ?411 1 0H. Gently shake the mixture. Positive result; the para isomer turns the mixture greci or blue, the ortho isomer turns itredtoviolet. (14). ------- R!SORCINOL Synonyms: B enzenediol, dihydrosybeazene, bydroxyphenol, resorcin. Descriptiorn White crystals that turn pink on esposare to light. Sweet taste. Sinks and dissolves. A common topical antiseptic. TDxicity: Local - Irritates skin in concentrations above 10%. Systemic - Moderate by ingestion. Aquatic - Moderate. Detection: Add dilute £erric chloride to sample. Positive result: solution turns violet. GALUC ACID, PYROCALLOL. PYROCATECROL. and related compounds also give a color reaction with ferric chloride. (1,4,6). ------- SAL ICYLALDEHYDE (OH)C 6 H 4 (CHO) Synonyms: Hydroxybeuzaldehyde salicylal, salicylic aldehyde. Descriptiorn Colorless oily liquid or dark red oil (depending on purity and exposure). Rifler almond odor, burning taste. Sinks; slightly soluble. Combustible. Toxicity: Human - Low. Aquatic - High for algae, low for fauna. Detection: (I). Detect as an aldehyde (see PEWFMLAL for methods). ( ii ). Mix 2 ml of sample with 2 ml of ethanol and I ml of 0. SM Co(NO 3 )z. Add 1 nil of 0. 1% o-phenylenediamine in dilute acetic acid. Positive result: mixture turns orange- red. (1,4). ------- 5&LIGYLIC ACiD (HO)C 6 H 4 (COOH) Synonym: Hydroxybentoic acid. Description: White crystalline solid; gradually discolors in sunlight. Sinks; slightly soluble. Any trace of iron turns the acid and its salts red. The common alkali salts are soluble. A common Iceratolytic. antimicrobiaL and fungicide. totcity: Local - May irritate skin of some people. Systemic - Low. Aquatic - Moderate. Detection: Acidify the sample with HC1 until just acid to litmus. Mix 2 ml of sample with 2 nil of 0. 9% ferric chloride solution and 2 ml of 1:10 acetic acid. Positive result: mixture turns violet. (1, 4, 6). Note that many other hydroxybenzene structures give a color reaction with FeCl 3 (see GALLIC ACID, PYROCATECHOL, PYROGALLOL, RLSORCJI4OL). ------- SELENIUM Se Includes: Selenium compounds. Descriptiorn fl nental selenium exists in several forms! amorphous (dark red to black powder), crystalline (dark red), end metallic (gray to black crystals). Sinks; insoluble, but there are several colloidal forms. Many Se compounds are commercially important. They include .elenic acid (very solubleL selenous acid (very soluble), sodium seleni te (very soluble), the oxide (very soluble), the halides and oxyhalides (soluble or decomposed by water to soluble products); a few compounds are not solubie or only very slightly soluble (hexafluoride, talkyl- dithiocarbamate, and sulfide.). Toxicity: Local - Low, except for the finning oxyhalides, which are corrosive poisons. Systemic - lEgh by inhalation otherwise low. Aquatic - Uncertain; there is some evidence that Se is a cumulative poison. Because Se attacks suiThydryl enzymes, it is probably more toxic to animals than to plants. Detection: Add 2 nil of concentrated sulfuric acid to 1 ml of sample; then add 0.5 g of NaIGO 3 . Heat to boiling Sr 1 minute. Positive result: mixture turn red or a red precipitate form. Starinous ion iiterferes. (25). ------- ilLYER Ag hclMes: Silver compounds. Description: Silver and its compounds denature proteins, and are often used as antiseptics. Many are sensitive to light, and are widely used in photography and printing. Toxicity varies with solubility. Of the common compounds, the following are soluble: chlorate and perchiorate, fluoride, hyponitrite, lactate, nitrate (lunar ti, permanganate, picrate, and selenate. The following have limited solubility: acetate, brornate, chlorite, chromate and dichromate, iodate, nitrite, and sulfate. The foUowing are practically insoluble: arsenate . bromide, carbonate, chloride , cyanide, iodide, oxalate, oxide, phosphate , and sulfide . Many common natural con- ditions will lead to the precipitation of silver from solution, since the carbonate, chloride, phosphate, oxide, and suJ.Sde are practically insoluble. The insoluble forms are mostly off-white, gray, or black. At suspected spill sites, it is important to collect samples of bottom sediments and milky or grayish suspensoids, which may be dissolved in nitric acid and then tested for the silver ion by the methods given below. Tesicity (N. B. Varies with solubility). Local - Caustic if very soluble; irritant otherwise. Systemic - The nitrate is a corrosive poison; other- wise, low to moderate. Aquatic - High. Dtdiorn Use Z test tubes. To each add 3 nil of O.ZS , (NH 4 ) 2 Ce(NO 3 ) in 1% RHO 3 and 2 ml of dilute RCL To one tube, acid I ml of reagent: to the other, add I ml of water. Positive result: sample decolorises the yellow ceric aznrnonium nitrate solution more rapidly than the water. Mn, ferrous, and sta.nnous ions interfere. (1, 4). ------- SLUDGE, CEEMICAL (from water supply treatment) Descriptioxu There are two types of ‘ CJLenuCa1” sludge from treatment of water supplies. One is largely organic, and results from the coagu- lation and precipitation of suspended matter with the aid of aluminum or iron compounds which enhance i2occuiat.io t. The other is largely in- organic. and results from water softening pro- cesses; it is principally calcium and magnesium compound.. A. third type of sludge from water treatment is organic. It result . from the backwashing of filters, and is essentially similar to the sus- pended microbiota in the water body from which the supply was drawn. I t is at organic sli me Toñcity: Aquatic only - The aluminum or iron from coa u- lants may be mobilized by chemical or biological action and develop a moderate ton city to the aquatic biota. The calcium and magnesium from softening arc not a toxic hazard but rnrp amage bottom life by sedimentation, or gill aac ñher membrane by blanketing. Organic sludges also threaten oxygen depleton through increased BOI l Detection: For alutninwn and iron, see ALUMINUM EU LFATE and FER.RJC HYDROXIDE. For softening products, test for calcium: see CALCIUM CARBIDE. For organic material, depleted oxygen or in- creased ROD. ------- SLUDGE, DIGESTED SEWAGE Description: Hearj, brown, often malodorous, fairly homogeneous slurry that is rich in organic matter and microbial netabolites. toxicity: See SLUDGE, RAW UNDIGESTED SEWAGE. Comments are generally applicable here. The hazard of human infection is diminished. Detection: As for raw sludge, high BOD is the main indicator. If the waters are naturally clear, turbidity will be seen if there has been a heavy discharge. ------- SLUDGE, RAW UNDIG TED SEWAGE Descriptkni Heavy brown slurry, carrying garbage. at rats • other “sanitary” wastes. There are two Pfl iPaI hasards: the Immediate threat from microbal pathogen., and a longer-term effect of increased BOD. Spills may occur from land or water barns veMdn or fro m pipelines and Tonicity: The infective h 5 sae4 is likely to be more than from whole snag. because bacteria and virus a are effectively precipitated with th. sediment and rema in table. Chanical contaminants are similarly concentrated. Adsorbed pesticide. may b.cane desorb.d. Boron has been shown to adsorb on sludge.. Ammonia and other natricts may be high, and also soluble sulfides. Detactiost Organic components by POD. Chezmcal components by apprupriate test based on other evidence as to probable presence. Bacteria and viruses cannot be detected rap i dly in the field. ------- DTUM Na Spaonym: Natriuni. Description: Soft, silvery metal that reacts violently with water to form SODIUM HYDROXIDE and hydrogen. Metallic sodium is stored and shipped in air-tight containers or immersed in naphtha. Severe fire risk in contact with water. Toilcity: Local - The metal causes severe skin burns. Systemic and Aquatic - See SODIUM HYDROXIDE. *ection: Use pH indicator or meter to test for strong base. Tests for the sodium ion are of limited value because sodium is normal constituent of most water, usually the most prevalent metallic one. A simple test is as foUows. Neutralize the samples with 3N HC1. To 2 ml of the neutralized sample, add 8 ml of zinc uranyl acetate reagent. Positive result: yellow precipitate. (2, S,6). ------- SODIUM ARSENATE Na 3 AsO 4 and Na 2 HAsO 4 Synonyms: Trisodium arsaiatt, dibasic sodium arsenate, diso&um arsenate. Descriptiorn Clear, colorless crystals. Mild alkaiine taste. Very soluble. The water solution is alkaline to litmus. Toricitr Human - Iügh. Aquatic - High. ft has been reported that some fish can tolerate concentrations of 2000 ppm for 3 hours. Detectiorn Tests for Na are of limited utility; see SODIUM. The £504 is the toxic component see LEAD ARSENATE for methods. ------- K)DIVIM AZ IDE ItN 3 Synonyms: None common. Description: Colorless crystals that sink and dissolve. On heating, it decomposes into sodium and nitrogen. ro city: Human - High by ingestion, otherwise low. Aquatic - High. D ection: Mix 2 ml of sample with 2 ml of arninonium sulfide solution and 2 ml of 0. IN iodine solution. Pos itive result: immediate evolution of bubbles of nitrogen. (1, 5). This test cannot begin to detect sodium azide in toxic concentrations; it is only useful where the concentration is well above the ppm range. ------- SODIUM BISULFITE NaHSO 3 and Na 2 S 2 O 5 N. B. The sodium bisul.fite of commerce is chiefly the metahis ulflte, Na 2 5 2 0 5 . SyN)flytnS Sodium add sulfite, sodium metabisulfite, sodJ urn hydrogen sulfite. Descri0n White, crystalline solid. Sulfurous odor and taste. Unstable in air, gradually oxidized to the sulfate. Sinks and dissolves. The solution is add. toxicity: Local - concentrated solutions may irritate skin. Systemic - Low. Mualic - Moderate to low. Other - Look for bleaching effects. Detection: tests for Na are of limited utility; see SODIUM. Test for bisulfite as follows. Use Z test tubes. To each add I ml of sample. To tube A 1 add 1 ml of 5% formaldehyde. Then add I ml of 0. 1N iodine solution to both. Positive result: iodine is de- colorized in tube B, but is not decolorized in tube A. (1 ,4 ,6). Commercial kits are available for detecting sulfites (including bisulfites); suppliers include Larnotte Taylor Hellige, and Mach. Sensitivity range is Z-300 ppm. (14,6). ------- SODIUM CHR.OMATE Na 2 CrO 4 Synonym: Neutral sodium chromate. Description: Yellow, somewhat deliquescent crystals that sink and dissolve, giving an alkaline solution. Toxicity: Local - Irritant; corrosive in high concentration. Systemic - Moderate by ingestion; low by skin absorption. Aquatic - High to moderate. Detection: Tests for Na are of limited utility; see SOD iUM. See AMMONIUM CHROMATE for chrornate tests. ------- SODIUM CYANATE NaOCN Synonyms: None common. Descriptzion White crystalline solid that sinks and dissolves. The cyanate ion is slowly convefled to cyanide; see BARIUM CYAMDE, POTASSIUM CYANIDE, and HYDROCYANIC ACID. toxicity: Human - Low, except by ingestion. Aquatic - Moderate and persistent. Detection: Sodium tests are of limited utility; see SODIUM. Test for cyanate as follows. Mix 2 nil of sample with I rut of cupric nitrate soludon and I mA of 0. 8% aqueous pyridine solution. Positive result: mixture turns red. (1,5,6). ------- SOD iUM CYANIDE NaGN Synonym: C yanog ran. Descriptiont White crystaUine solid. Odorless when dry; when damp, emits alight odor of HYDRCCYANIC ACID. Freely soluble. The aqueous solution is strongly alkaline and rapidly decomposes, form- ing a toxic layer of hydrogen cyanide at the water surface. Once widely used in pesticides, but now widely replaced by POTASSIUM CYANIDE. To x icityt Human - High and fast-acting by ingestion and inhalation of hydrogen cyanide vapors. Risk of absorption through injured skin. Aquatic - High. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Na tests are of limited utility; see SODIUM. See BARIUM CYANIDE and HYDROCYANIC ACID for CN tests. ------- SODIUM DICHROMATE Na 2 CrzOi Synonyms: Sodium bichromate, bichromate of soda. Descriptiorn Bright scarlet crystalline solid. Very soluble. The solution is acidic. toxicity: Local - Irritant and caustic. Systemic - Moderate by ingestion, low otlierwis a. Aquatic - Moderate. Detection2 Na tests are of limited utilitr see SODIUM. See AMMONIUM DICHROMATE for dichrornate tests. ------- SODiUM FEBRICYANIDE Na 3 Fe(CN) 6 Synonyms: Red pruniate of soda, sodium hexacyaixeferrate (UI). Description: Ruby red deliquescent crystals that sink and dissolve. Exposure slowly liberates hydrogen cyanide. To.tcitr Human - Low. Mi lafic - Reports vary widely; sometimes High. Detecion: Na tests are of limited utility; see SODIUM. See AMMONIUM PERRICYANIDE for ferricyanide tests. ------- SODiUM FERROC’YANIDE Na 4 Fe(CN) 6 Synonyms: Sodium hexacyanoferrate (U) sodium prus slate yellow, yellow prussiate of soda. Descriptioxu Pale yellow , s ernitransparent, cr ystailine soli& Exposure to sunlight and strong acids over time liberates hydrogen cyanide. Toxicity: See SODIUM FERIUCYANIDE. Detection: Na tests are of Utnited utility; see SODIUM. See AMMONIUM FERROCYANIDE for ferrocyanide tests. ------- SODIUM FLUORIDE NaF Synonyms: Via rocid, flura- Drops, Karidiurn, Villiaumite, Z yniafluo r - Description: Clear, shiny, crystalline powder, Insecticide grades are often tinted blue. Household insecticide grades must be tinted Nile blue. Sinks and dissolves. The water solution is mildly alkaline, and react8 with silicates. toxicity: Local - Concentrated solutions are irritant. Systemic - Moderate to high. Aquatic - Moderate to high. Detection: Na tests are of limited utility; see SODIUM. See ALUMINUM FLUORIDE for F tests. ------- SODIUM FLUOSILICATE Na 2 SIF 6 Synonyms: Sodium flnorosilicate sodium silicofluc ride. Description: Tasteless, odorless, white crystalline solid. Sink, and dissolves. Toxicity: Local - Irritant , Systemic - Moderate by ingestion and inhalation , Aquatic - Moderate. Detection: Na test. are of limited ufility see SODIUM. Test for fluosilicate as follows. Mix the sample with 3M NeON. A gelatinous precipitate occurs if fluosilicMe is present. ------- SODIUM HYDROSULFIDE Na * Synonyms: Sodium bisulfide, sodium sulThydrate, sodium hydrogen sulfide. Description2 Colorless to lemon- colored crystaffine solid. Very hygroscopic. Readily hydrolyzed in moist air to SODIUM HYDROXIDE and SODIUM SULFIDE. Sinks and dissolves. Weakly alkaline. Hydrogen sulfide slowly liberated in the presence of water and carbon dioxide, giving the characteristic odor of rotten eggs. Toricitr Local - Irritant. Systemic - Low. Aquatic - High to moderate. Other - Very oxygen- dernarding; may drastically reduce DO. Look for discoloration on rocks and structure.. May taint the flavor of fish. Detection: Na tests are of limited utility; see SODIUM. To test for hydrosulfide, mix the sample with 3M NaOH. Then test for suilide ion (see AMMONIUM SULFIDE for method). ------- SODIUM HYDROXIDE NaOH Synonyms: Caustic soda, lye, sodium hydrate 1 white cau3tic. Description: DeJ.iquescent. white, very corrosive solid. Absorbs water and CO 2 from cdr. Sinko; vety olable. A. powerful alkali base. Aqueous sci.utione fGel aiJy Toxicity: Local - Powerfully caustic: b urns and trntates tin sues. Systemic A corrosive P 0 lCO 1 r moderately toxic by ingestion. Aquatic - High to moderate. Other - Look for corrosion effects. WEAR PROTECTWE CLOTHING. Detection: Use pH indicator to test for strong base. (1 . 3}. Na tests are of limited utility; see SODIUM. ------- SODIUM METHYLATE I-5CONa Synonym: Sodium methoxide. Description: FIow5.tg white powder. Sensitive to oxygen. Decomposed by water to METHANOL and SODIUM WY DROXIDE. Toxicity: See METHANOL and SODIUM HYDROXIDE. Detection: See METHANOL and SODIUM HYDROXIDE. ------- SODflTh& NITRITE Na140 2 Synonyms: DtawtIsi salts exinitrit. flescriptiorn WMte to ye l lowish hygroscopic solid. Very slowly oxidiaes in air to sodium nitrate. Sinks arid dissolves easily. Decomposed by even weak acids to evolve fuming nitrous enhydride. The aqueous solution is weakly a lkaline. Toxicity: Human - )hederate. Aquatic - Moderate to high. Dt.cliou Its tests are of limited utiuity see SODIUM. To detect nitrite, mix 2 ml of sample with 2 ml of 06% snjfap ilic acid in 20% HCJ.. Let st -s M S minutes. then add 2 ml of 0. 4% alphs-napbthylaatine MCi in 1% MCi. Putative result solution turns reddish purple. (2 ,54). ------- SODIUM OLEATE C 17 H 33 COONa Synonyms: Oleic acid sodium salt, Eunatrol. Des criptiorn White powder; slight odor of tallow. Dissolves in water, giving a mildly alkaline solution. A component of many kinds of soap. Combustible. Toxicity: Human - Low. Aquatic - Moderate to high. Other - Foams and suds; may cause a “bathtub ring” precipitate in hard water. Detection: Add a few drops of methyl orange indicator to 10 ml of sample; then acidify with 1:1 sulfuric acid. Extract this solution with 1:1 petroleum ether and ethyl ether. Evaporate the solvent on a steam bath, then test the residue for OLEIC ACID (see that entry for method). (1,4). Alternatively, high concentrations of any fatty acid or soap may be detected as follows. (1) Acidify 5-jo ml of sample with 1:1 sulfuric acid. Fatty acids will rise to the surface as an oily slick. (2) Prepare reagent as followet Add a few drops of Nile blue sulfate to 5 ml of dilute sulfuric acid and boil for 5 minutes. (3) Add a few drops of the reagent to the oil-slick mixture; stir well and let stand a few minutes. Positive result: fats and fatty acids will preferentially absorb the dye; fats wiU be stained red, and fatty acids will be stained blue. (1,4). ------- SODIUM PALMJTATE H 3 C(CH 2 ) 14 COONa Synonyms: Sodium cetylate. sodium hexadecanoate, sodA urn hexa* lety late. Description: A characteristic household soap (bath, toilet, and laundry). A white solid available in many commercial forms (cakes, flakes, powders, etc.). Toxicity: Human - Low . Aquatic - Moderate to high. Other - Foams and suds; may cause ‘bathtub ring’ precipitate in hard water. Detection. There Is no suitable method for detection of low concentrations at water’s edge. in an improvised laboratory, identification may be performed as follows. Add a few drop. of methyl orange indicator to 10 ml of sample and acidify with 1:1 sulfuric acid. Extract the solution with 10 ml of 1:1 petroleu m ether and ethyl ether. Evaporate the solvent on a steam bath Then transfer the residue to a round- bottom S flask. Add to the flask 5 ml of UT. B1 3 in methanol and reflux on a steam bath (or 2 minutes. Let co d. Then extract with 10 ml of n-pentane. Analyze the methyl pa l mnitate formed by CC. (14,6). High concentrations may be detected using the alter- native method given for SOD iUM OLEATZ. ------- SODIUM ?HOSPHA.T E Na 3 PO 4 , Na 2 HPO 4 , NaHzPO 4 t Na 4 ? 2 0 7 , Na 2 H 2 P 2 O 7 Synonyms: AU the common forms are included: tribasic (teft), dibasic (sec), monobasic (prim) sodium phosphate, as weU as normal (tetra) sodium pyrophosphate (TSSP) and acid (disodium) sodium phosphate (TASP). Description: All are white crystalline solids that dissolve readily. Na 3 PO 4 is very alkaline, NaHzPO 4 is acid; the others are slightly alkaline. Totcity: Human - Low. Aquatic - Moderate to low, depending on the form. Na 3 PO 4 is the most toxic, Na 4 P 2 O 7 the least tori c. Other - Phosphate is a plant nutrient that may stimulate plant and algal growth. Detection: Na tests are of limited utility; see SODIUM - See AMMONIUM PHOSPHATE for phosphate tests. ------- SODIUM SILICATE Vanes from Na 2 0 • 3.75 SiO to 1 Na 2 0 S b 2 Synonyzn Water glass. Description: Depenhling on the composition, lumps of greenish glan or white powders (soluhility varies) or liquids nrying from clear and flawing to cloudy and viscous. Forms gels with acids over a wide pH range (3-9). It is coagulated by brine and precipitated by alkaline earth and heavy metal ions. Many forms are strongly alkaline in solution. Hwnan - Low. Aquatic - Low. Other - Fouling of shores and surfaces with lumps and gels. Detection: Na tests are of limited utility; see SODiUM. Detect silicate as kllows. Acidify the sample with 3M HCI; a gelatinous precipitate mdicates that the silicate ion may be in the sample. (1, 5,6). ------- SODIUM STEARATE C 17 H 35 COONa Synonyms: Sodium octadecanoate, stearic acid sodium salt. Description: White powder; fatty odor; soapy feel. Sinks and slowly dis solves 1 forming an aikaline solution. A soap often used in toothpastes and cosmetic preparations. Toxicity: Human - Low. Aquatic - Moderate to high. Other - Foams and suds; may cause a ‘bathtub ring” precipitate in hard water. Detection: Na tests are of limited utility; see SODIUM. Detect paimitate as a soap; see SODIUM OLEATE and SODIUM PALMITATE for methods. ------- SODIUM SULFWE Na 2 S Synonyms: S odium monosulfide , sodium sulfuret. Description: Yellowish crystalline solid that discolors on exposure to air, turning brick red and finally black. Commercially available as crystals, lumps, and flakes. Rotten-egg odor of hydrogen sulfide. Sinks and dissolves freely, giving a strongly alkaline solution that liberates hydrogen sulfide as it is exposed to carbon dioxide and acids. Toxicity: Local - Irritant; do not handle with bare hands. Systemic - Low; vapor hazard from hydrogen sulfide. Aquatic - Varies from high to low. Other - Very oxygen-demand; may drastically reduce DO. Look for discoloration on rocks and structures. May taint the flavor of fish. Detection: Na tests are of limited utility; see SODIUM. See AMMONIUM SULFIflE for sulfide methods. ------- SODIUM SULFITE Na 2 50 3 Synonyms: None common. Descriptiorn White crystals or powder. Saline, sulfurous taste. Sinks and dissolves, forming a slightly alkaline solution. A widely used bleaching agent and preservative, a reducing agent and a sub- stitute for “Hypo” in plitography. toxicity: Human - Low. Aquatic - Moderate to low. Other - Look for bleaching effect, especially on plants. Detection: Na tests are of limited utility; see SODIUM. See FERROUS SULFITE for sulfite methods. ------- SODIUM THIOCYANATE NaSCN Synonyms S odium sullocsranate, sodium rhodanide, sodium rhodanate. sodium sulfocyanide. Descrijtoin Colorless or white deliquescezat crystals. Sink awl dissolve, lowering water temperature considerably. Toilc ity: Human - Low (the cyanide effect is t involved). MnUc - Moderate. Detection: Na tests are of limited utility; see SODIUM. See AMMONIUM THIOGYANATE for thiocyanate methods. ------- SODIUM TUIiGSTATE Na WO 4 Synonym: Sodium woLframate. Description: Colorless crystals or white crystalline powder that sinks and dissolves The solution is slightly alkaline. Toxicity: Htnnan - Low. Aquatic - Moderate. Detection: Na tests are of limited utility; see SODIUM. Test for tuztgstate as follows. Mix 2 nil of samples with I nil of concentrated HC1 and 1 nil of 10% KSCN solution. Add to it 2 ml of Iresbly prepared 20% SnCl 2 in concentrated HCI. Positive result: solution turns bluish-green. fluoride and selenium interfere. p5 .6). ------- SORBJTOL CH 2 OH(HCOH) 4 CH 2 OH Synonyms: Glucitol, gulitol , henhydric alcolxil, sorbit, and a variety of proprietary trade names. Description: Colorless crystalline solid. Hygroscopic and combustible. Odorless; sweet taste. Sinks and dissolves freely; concentrated solutions are syrupy. Widely used as sweetening agent, burn ectant, phar- maceutical vehicle, and antifreeze. Totcity Human and Aquatic - Practically none. Other - Raises SOD.. Detection! Detect as a glycol; tee ETHYLENE GLYCOL for method. ------- STANW)US CHLORIDE SnCI, Synonyms: Tin dichloride, tin protochloride. tin crystals, tin salt. Description White crystalliae mass or üakes; fatty appearance. A powerful reducing agent. It absorbs oxygen (ron-i the air to form an in- soluble oxychioride. It dissolves in water, but in great dilution it forms an insoLuble basic salt. Toxicity: Local - !rritsnt to skin and. mucous mnernhr.via: Syc’t-ennc - Low. Aquatic - 1-Egh . Detection: It i G important to collect bottom samples and filter samples Iro n- i cloudy waters because SiC ! 2 is convened by natural processes ir to inso luble products when exposed to water and air. 8oil suspect samples in aqua regia to redissolve the tIn, then proceed as follows. (I ). Mix the sample with O.1N ammonium sui!Wc. Positive result brown prc- cipitate. çl,4L (U). Mix the sample with 0. 114 mercuric chloride. Positive result: white to gray precipitate. (1.4).. See AMMONItTM CHLORIDE for Cl tests; they an of limited utility compared to Sn tests for this compound. ------- STRONTIUM CLUOR WE SrCI 2 Synonyms: None. Descri$iot Odorless, white, crystalline solid, deliquescent in i st air. Sharp, bitter taste. Sinirs and di.- solves resdily. itriurover, wha erposal to COB, the nearly insoluble white carbonate is formed. Toric itp fiman - Ln. Muatic - Moderate. Detectosv ft Is lznportam to calect bat’o- 0 samples and filter samples from cloudy waters because the Sr ion is precipitated as the insoluble white carbonate in the presence of carbon dioxide. Boil suspect samples in aqua regis. to ndinoln the Sr, then proceed as b3IiSws. AM several drop. of saturated K 2 CrO 4 to Z ml of sample. Ld stand kr one minute. Then add! ml of 0. Z% rhediseast. solution (which must be fresh). Positive rest solution turns reddish brown. (1, 5). Set AWCNIW CIOCRIDE ior C! tests; they are of united tlity cr ared to the Sr tests for this ------- STRONTIUM NITRATE Sr(N0 3 ) 2 Synonyms: None. Description: White crystalline solid. Sinks and dissolves readily. Strong oxidizing agent. When the water solution is exposed to GO 2 , the nearly insoluble white carbonate is formed. Toxicity: Human - Low. Aquatic - Moderate to low. Detection: See STRONTIUM CHLORIDE for Sr methods. See AMMONIUM NiTRATE for nitrate tests; they are of limited value compared to the Sr tests for this compound. ------- STYR.ENE C 6 H 5 (CthCH 2 ) Symrnyms: Cinnamene, cinnaniol, phenyl ethy lent, styrol, styrolene. Description: Clear, colorless, very refractive, combustible oily liquid. Sharp aromatic odor. floats; sparingly soluble. On exposure to heat and light, it slowly polymerizes and is oxidized. Polystyrene is a clear solid plastic, slightly heavier than pure water and in- soluble in it. Toricityt Local - Liquid and vapor irritant. Systemic - Low. Aquatic - Moderate. Other - Fouling of surfaces by polystyrene. Detection: Detect as an unsaturated compound: see BENZENE for methods. ------- SULFUR CHLORIDE S 2 C 1 2 Synonyms: Dis ulfur dichlo ride, sulfur monochlo ride, sulfur subchloride. Description: Amber to yellowish-red, oily, turning liquid. Sharp, penetrating odor. Decomposes on contact with water to give HYDROCHLORIC ACID, SULFUR DIOXIDE, SULFUROUS ACID, hydrogen sulfide, thiosulfate, and other acid products. Toxicity: Local - Extremely corrosive and irritating. Systemic - A corrosive poicoi-t. Moderate. Aquatic - Moderate. Other - Lock tot corrosion effects. WEAR RESPIRATOR AND PROTECTiVE CLOTHING. Detection: Detect as sulfide 1 sulfite, chloride, etc. For methods, ace AMMO ?4IUM SULFIDE, FERROUS SULFITE AMMONLUM CHLORI DE, HYDROCHLORIC ACID, SULFUR DIOXIDE, SULFUROUS ACID. In addition, test for thio- sultate as follows. Miii rn! ot a ample with 1 ml of 3% Na N 3 a: d. 2 nil of U . iN iodine solution. Positive result: iinzned&ate evolution of gas bubbles (nitrogen). (1, 4). ------- SULFUR DIOXIDE 502 Synonyms: Sulfurous anhydride . sulfurous oxide. Description2 Colorless, nonflammable gas. Strong suffocating odor. Commercial form is liquefied gas. In water, the gas is in equilibrium with its formed acid (SULFUROUS ACm), which is a corrosive add and a strong bleaching agent. Under the action of sunlight, it is gradually oxidized to SULFURIC ACID. Toxicity: Local - Very irritant liquid and vapor. Systemic - High by inhalation; otherwise moderate. Aquatic - (Moderate); a corrosive poison. Other - Look for corrosion damage to plants, shore- line, and structures. WEAR RESPIRATOR AND PROTECTIVE CLOT HINt). Detectiorn The strong odor and the acid pH can be used to foflow the spi 1 i in moderate concentration. For detecting the dilute acid and gas, commercial kits are available; sensitivity range is 1-400 ppm. Suppliers include Kitagawa. MSA. and Scott/Davis. for 2,5,6). ------- SULFURIC AC H 2 S0 4 Synonyms: Hydrogen sulfate, oleuni, spent sulfuric acid, oil of vitriol, buttery acid. Description: Strongly corrosive, dense, oily liquid. Colorless to dark brown, depending on purity. Miscible with water in all proportions. The concentrated acid reacts violently with water. Reacts strongly with metals and many organic compounds. Some grades are fuming and hygroscopic. The fuming, concen- trated grade is commonly called “oleum” on shipping labels. Toxicity: Local - Extremely irritating vapor; liquid causes severe burns. Systemic - A corrosive poison; moderate. Aquatic - Moderate. Other - Look for corrosion effects on shorelines and structures. Detection: Use pH indicator to detect acidity. Then test for sulfate ion (see ALIJMXN1JM SULFATE for methods). ------- SULFUROUS ACID 112803 Synonym: Sulfur dioxide solution. Descriptiorn A solution of about 6% SULFUR DIOXIDE in water. Clear, colorless liquid that gives off the sharp, saUocating odor of SULFUR DIOXIDE. Corrosive and bleaching agent. Gradually oxidizes to SULFURIC ACID. toxicity; See SULFUR DIOXIDE. Detection: See SULFUR DIOXIDE. ------- SUPERPHOSPHATE A mixture of calcium phosphates, calcium sulfate, iron oxide, silica, etc. Includes: Triple superphosphate. Description: The most important phosphorus fertilizer. White to grayish powders or granules. Sinks; solubility varies with the composition of the mixture, but usually slightly soluble. Toxicity: Human - Low. Aquatic - Varies with solubility; usually low. Other - Superphosphate is a fertilizer, and may stimulate the growth of algae and noxious plants. Detection: See AMMONIUM PHOSPHATE for phosphate tests. Ca tests are of limited utility. ------- TANN1C ACiD Variable structure, depending on origin; one important variety is empirically C 27 HSaO 4 6 Synonyms: Tannin. gallotannin. gallotannic acid 1 corilagin , nutgall extract. Deacriptiorn Yellowish to light brown amorphous,. bulky powder or flakes or spongy manes. Faint characteristic odor like tanned leather. Gradually darkens on e r- posure to air and light. Sinks; very soluble. Totcity: Local - May dry and discolor skin. Systemic - Low. Aquatic - High. Other - Discoloration of structures. Detection: Boil a mixture of 0. 05% g of sodium tungatate. 0. OZ g arsenious oxide, and 2 ml of ZN MC i. Add to this mixture 2 ml of sample and 2 ml of 20% sodium carbonate solution. Positive result: solution turns blue. U.5). ------- TETRAETHYLENE PENTAMfl % E HZN(C 2 HNH)CHNHz Synonym: TEPA. Description: Viscous, hygroscopic liquid. Amine odor. Floats and dissolves. Combustible. Toxicity; Local - irritant. Systemic - Moderate. Aquatic - (Moderate) . Detectiorn Detect as a primary amine and a secondary amine (see DIAMYLAMINE, PROPYLAMINE, and PYR1DINE for methods). ------- THALLIUM 11 Includes: Common thallium compounds. Description: Thallium is a bluish white, soft metal that forms a skin of oxide in air. The metal and all of its most important compounds are poisonous, and are widely used in pesticides, as well as in many industries (metallurgy, electronics, optics. pyrotechnics). The soluble compounds are white to yellow crystals. The relatively insoluble forms include the halides (white to yellowish crystals) , the sesquioxide, the sulfide, and the selenide (all dark crystals or powders). In contrast to many heavy metals, both the hydroxide and the carbonate are quite soluble, and except for the sulfide and the high-valence oxide, all the usual derivatives that might be formed after a spill in water are at least slightly soluble. Toxicity: Human - High. Aquatic - (High). Detection: Treat suspect solids with IM sulfuric acid to dissolve the TI. Use the following test for the Thou. Mix2rnlofsaznplewith 2 ml of 10% KL After a white precipitate forms, add 3 nil of 2% Na 2 S 2 O 3 . Positive result: the white precipitate turns yellow. Pb and Ag interfere. (1, 5). ------- THIOGLYCOLIC ACID HSCH 2 COOH Synonyms: Mercaptoacetic acid, thioglycollic acid. Description: Colorless liquid. Strong, unpleasant odor. Miscible with water. Readily oxidized by air to hydrogen sulfide and ACETIC ACID. Toxicity: Local - Irritant; can severely burn and blister skin. Systemic . Moderate. Aquatic - (Moderate ). Detection: The odors of hydrogen sulfide and acetic acid, and a somewhat acid pH can be used to detect fairly high concentrations. Also see ACETIC ACID; to detect sulfide, see AMMONIUM SULFIDE. Test for the thioglycolate moiety as follows. Mix 2 ml of sample with 2 ml ol 8% sodium acetate sclution aad 1 ml of 5% acfli acid. Add .i ml of 37% formaldehyde solution, and set aside for 2 minutes. Then add 2 ml of phosphotungstic acid reagent (10 g of sodium t rngstate in 80 nil ‘of 10% phosphoric acid). Positive result: solution turns blue. Mercaptans interfere. (1. 5). ------- THOIULJM CHLORIDE ThCl 4 Synonyrrn Thorium tetrachioride. Description: Colorless to light yellow crystalline solid. Hygroscopic; partially volatile. Sinks and dis solves. toxicity: Local - irritates mucous membranes. Systemic - Moderate. Aquatic - High. Detection: Detect thorium in solution by mixing samples with a buffer solution (4. 1% sodium acetate and 2. 9% glacial acetic acid) that contains 0.02% carmiriic acid. Posi- tive result: the solution tun is yellow. Ft aria A.! inter- fere. (1,5 1. ------- THORIUM NITRATE Th(NO 3 ) 4 Synonyms: None. Descriptiorn White crystalline mass that sinks and dissolves freely , giving an acidic solution. A strong oxidizing agent. Toxicity: See THORIUM CHLORIDE . Detection: See THORIUM CHLORIDE for Th method. See KMMONBJM NITRATE for NO 3 methods. ------- TITANIUM COMPOUNDS Ti and its compounds Includest The elemental metal and its common compounds .. - halides, hydride isopropylate , oxalate, oxide, sulfate, and complex salts with axmnothwn and potassium; includes titanate, titanous, and titanyl compounds. Description: titanium metal ‘s shiny, gray, and insoluble in water; it is widely used in metallurgy. Its halides oxysulfate (titanyl sulfate, TiOSO 4 and isopropylate are unstable, and are decomposed on contact with moist air or nter, often yielding highly irrita t ing decomposition product.. The alkali complexes are all water soluble. The sesquisulfate (titanous sulfate) and the coznxnsrcially very important dioxide (Unitane, titania) are insoluble; the powdered dioxide is widely used as a pigment for white paint 1 and the crystalline dioxide is used to make imitation thamonds. The oxide ozysulfate and tetrafluondc are white powders; the isopropylate and tetrachioride are unstable fuming liquids. Several of the salts give highly colored solu- tions tusually reddish purple), but these solutions are generally unstable , particularly when organic matter, oxygen and other metals axe present Toxicity: Local - Dust, and decomposition products are irritants. Systemic. Low, except the hydride. which is highly toxic. A Quatic - High. Toxicity it lower an hard than in soft Water. Other - Unstable titanium compounds may cause corrosion damage. Detection: Ti compounds often react with water to form insoluble precipitates: be certain to collect samples of suspect bottom solids and suspended solids. Both solids and liquids may be analysed as follows. Evaporate the sample to dryness. Fuse the abed solid with potassium pyrosuif ate until effervescence ceases. Then dissolve the cooled juts & in 10% H S0 4 by boiling. Positive reactions are? (1) hydra- gen peroxide turns the solution yellow or orange; 2) rnor- phine turns it red. (1, 4). ------- TOLUENE (H 3 C )C 6 H 5 Synonyms: Methylb enzene, phenylrnethane, toluol. Description: Colorless, refractive, flammable liquid. Odor like benzene. floats; very slightly soluble. Toxicity : Local - Liquid and vapor irritant. Systemic - Moderate to low. Aquatic - Moderate to high. RESPIRATOR AN]) PROTECT IVE CLOTHING ADVISABLE. Detection: Commercial kits are available; sensitivity range is 1-1000 ppm. Suppliers include Kitagawa, MSAS and Scott/Davis. (l 4,6). Alternatively, test for unsaturation (see BENZENE for method). ------- TOLUENE DIISOCYANATZ H 3 CC 6 H 3 (NCO)Z Synonyms: Diisocyanatotolueue tolylene diisocyanat e. TDI, Nac conate. Description: Colorless liquid at room temperature; freezes at about 70°F. Sharp, biting odor. Darkens on eicposure to sunlight. Reacts with water to produce 002 and diarninotoluene (toluene diarnine) , which is a colorless liquid, miscible with water, Totcity: Local - Very irritating vapor and liquid. Systemic - Moderate by ingestion. Aquatic - (Moderate to high). PROTECTIVE CLOTHING ADVISABLE. Detection: Analyze for primary amine; see PROPYLAMJNE for method. ------- TOLUIDINE H 3 CC 6 H 4 NHz Synonyms: Axninotoluene, methylaniline. Description: There are 3 isomers, all combustible and all slightly soluble. The rn isomer is a colorless liquid that floats on water; o is a pale yellow liquid that turns red then brown in air arid light, and may float or sink depending on temperature and dissolved solids; is a shiny white solid (plates or leaflets) that sinks. Toxicity: Local - Irritant to skin and eyes. Systemic - Moderate by ingestion, low by skin penetration. Aquatic - Moderate. PROTECTIVE CLOTHiNG ADVISABLE. Detection: Analyze for primary amines; see PROPYLAMINE for method. ------- TRICHLOROP$LENOL HOC 6 H 2 Cl 3 Synonyms: ColJ.unosol. Dowicide I and IS, Dotcide B , Trichiorer -. Description: Colorless to yellowish or gray solid (depending on technical grade 1 isomer, or derivative). Strong phenolic odor. Sinks; al most insoluble. The sodium salt sinks and dissolves, giving a markedly alkaline solution. Used as bactericide, !ungicide and defoliant. Taricitr Local - Strong irritant. Systemic - Moderate to high by all routes. Aquatic - 1*gh to fauna and flora. WEAR RESPIRATOR AND PROTECTIVE CLOTHING. Detection: Test for unnturafton (see BENZENE for method), for aromatic alcohol (see below), or for organic halide (see below). To test for aromatic alcohol, combine I ml of sample with S i n .! of reagent (a 10% solution of ceric axnmoniuni nitrate in ZN HNO 3 ). Positive resuTh brown to greenish brown precipitate (1, 3). To test for organic halide, to 2 ml of sample add S ml of freshly prepared 15% NaI in acetone (Do Not Use U the Iodide Baa Turned Reddish or Brown; it should be colorless). Positive result: reddish- brown precipitate. If test is not clear, put teat solution in hot water (alxnat 120°F) for 5 -10 minutes; if no precipitate forms test is negative. (1, 3). ------- TRIETHANOLAMINE (HOC}4 2 CH 2 ) 3 N Synonyms: TEA, trihydroxyethylamine. Description: Colorless, viscous, hygroscopic liquid that jells at about 70°F. Turns brown on exposure to air and light. Slight arnrnoniacal odor. Sinks and dissolves, giving a strongly basic solution 4 Corn- bustible. The article of corninerce contains a large quantity of di - and monoethanolamine. Toxicity: Local - Irritant, especially to eyes. Systemic - Low. Aquatic - Moderate. Detection: If the smell of ammonia is strong, test with pH indicator for a base. (1 3). In any case, test for tertiary amine by mixing 2 ml of sample with 2 ml of 1% methyl iodide. Positive result: precipitate forms. (1, 4). ------- TRiETHYLAM [ NE (C 2 H 5 ) 3 N Synonyms: None. Descriptiorn Colorless liquid; strong amnioniaca). odor. Floats; slightly soluble in warm water (above 66°F ); miscible with cold water. Very flammable. Toxicity: Local - Strong irritant , especially to the eyes and lungs. Systemic - Low 4 Aquatic - Moderate. Detection: Methods identical to TIUETHANOLAMINE. Commercial kits are also available; sensitivity range is 2 -ZOO ppm. MSA is one supplier (I or 2, 5,6). ------- T IUETHYLENETETRA.M INE H 2 N(CZH 4 NHZ)ZCZH 4 NHZ Synonym: TETA. Descriptiorn Clear, yellowish, viscous, volatile liquid. Slight arnmoniacai odor, floats; miscible. Toxicity: Local — Irritant liquid and vapor. Systemic - Low. Aquatic - Moderate to low. Detection: Analyze for primary and secondary amine; see DIAMYLAMINE and PROPYLAMINE for methods. ------- TR IMETHYLA}41NE (Gil 3 ) 3 N Synonym: TMA. Description: The article of commerce may be either a compressed liquefied gas or an aqueous solution. Both forms are highly flammable, and both have a sharp, fishy. ammoniacal odor and a salty taste. Readily miscible with waters giving a strongly basic solution. The hydrochloride and the oxide are also soluble. Toxicity: Local .- Very irritant vapor; liquid causes burns. Systemic - Moderate by ingestion and inhalation. Aquatic - High. Detectiorn Analyze for tertiary amine (see TRIETHANOLAMINE for method). Commercial kits are available: sensitivity range is 2-250 ppm. MSA is one supplier. (1, 5,6). ------- VANADYL SULFATE \0S 04 Synonyms: Vanath c sulfate, vanadium sulfate vanadium oxys ulfate. Description: Blue crystalline powder or crystals. Sinks and dissolves. Toxicity: Human - Low. Aquatic - Moderate to high. Detection: Add SN sulfuric acid to S ml of sample to acidify. Then add 1 ml of 10% phosphoric acid to S ml of acidified sample; this rcnoves interference from iron. Finally, add a few ml of 3% hydrogen peroxide solution. Positive result: solution turns reddish- brown. (1, 5, possibly 6). ------- VINYL ACETATE H 3 CCOOC}LC13 2 Synonyms: Ac eto ethylene. ethylene ac elate. Description A raw material for polyvinyl resins. Colorless, clear, liquid; sweet, pleasant odor. Very flammable. Polymerizes in light to a clear, colorless mass (polyvinyl plastic); inhibitors (such as I-{YDROQUINONE and diphenylarnine) are usually added to prevent spon- taneous polymerization. Both the liquid monomer and the solid polymer float, but the liquid is rather soluble, while the solid is insoluble. Toxicity: Local - Irritant; vapor harmful. Systen-uc - Moderate; most toxic by inhalation. Aquatic - Moderate. Other - Look for fouling by the polymer. RESPIRATOR AND PROTECTIVE CLOTHING ADVISABLE. Detection: Test for unsaturation; see BENZENE for method. ------- VINYL BROMIDE H 2 C:CHJ3r Synonyms: B romo ethylene, ethylene bromide. Description: Very flammable colorless gas that Iiquefies at 60°F. Sinks; insoluble. The gas is heavier than air. Polymerizes to form a clear plastic solid. Toxicity: Local - Irritant liquid and vapor. Systemic - Low. Aquatic - (Low ). Other - Look for fouling by the polymer. RESPIRATOR AND PROTECTWE CLOTHING ADVISABLE. Detection: Use two presumptive tests. Test for unsaturation (see BENZENE for method). Also test for organic halide (see TRICHLOROPH-ENOL for method). ------- VINYL CHLORIDE H 2 C:CHC1 Synonyms: Chioroethene, chioro ethylene, ethylene chloride, vc. Description: the most important vinyl monomer. Colorless gas with sweet odor; usual commercial form is compressed, liquefied gas; the liquid is clear and colorless. Spontaneously polymerizes in the light; phenol often added to inhibit polymerization. Floats; slightly soluble; very fla.rnrnable. The polyvinyl plastic is clear and insoluble; it floats. Totcity: Local - Irritant Iiquid and vapor; the liquefied form is very cold, and may cause severe frostbite. Systemic Low. Aquatic - Low. Other - Fouling of shorelines and structures by polyvinyl. PROTECTIVE CLOTHING AND RESPIRATOR ADViSABLE. Detection: Commercial kits are available; sensitivity range is 100-2000 ppm 4 Suppliers include MSA., and Scott/flats. (1, 5,6). ------- XYLENE C 6 H 4 (CH 3 ) 1 Synonyms: Dimethylbenz ene, methyltoluene, zylenol. Description: There are three pure isomers (rn, o, and but the xylene of commerce is an isomeric mixture, with the n-i isomer predominating. Clear, colorless, mobile, flammable liquid. Aromatic odor, similar to bensene. Floats; practically insoluble. Toxicity: Human - Low to moderate; most toxic by inhalation. Aquatic - Moderate. RESPLRATOR ADVISABLE. Detection: Commercial detectors are available: sensitivity range 18 10-5000 ppm. Suppliers include Kitagawa, MSA, and Scott/flats. (1,5,6). Alternatively, test for unsaturation; see BENZENE for method. ------- XYLENOL H0C 6 } 1 5 (CH 3 ) 2 Synonyms: Dixnethylphenol, hydroxydimethylbenzene; a constituent of ttcresylic acid”, a commercial mixture of CRkSOLS. Description: There are several pure isomers, but the article of commerce is a mixture of isomers. White crystals. Coal tar odor. Sinks; slightly soluble. Combustible. Toxicity: Local - Irritant to skin. Systemic - Moderate by ingestion, low by skin absorption. Aquatic - Moderate. Detectiou: Test for aromatic alcohol as fol lows. Combine 2 ml of sample with 5 ml of reagent (10% solution of ceric ammonium nitrate in ZN HNO 3 ). Positive result: brown to greenish-brown precipitate. ------- ZINC COMPOUNDS Zn and its compounds Includes: Elemental metallic zinc and all important zinc- containing compounds. Description: Metallic zinc is a shiny, bluish metal that quickly forms a dull white skin of carbonate in air. With few exceptions, zinc compounds are white, sometimes tinged with yellow or gray. Yellow or orange zinc compounds include the chromate hydroxide, dichromate, selenide, and tannate; dark gray or purplish or brownish Zn compounds include the perrnanganate, phosphide, and telluride. Most of the common salts are soluble: halides and oxyhalides, nitrate, sulfate, acetate. fonnate, etc. Several others are slightly soluble: bensoate. caprylate, chrotnate hydroxide, citrate, fluoride, lactate, oxalate, and nitrate. Several of the most important Zn com- pounds. however, are practically insoluble: carbonate and carbonate hydroxide cyanide, ferrocyanide, oxide, phos- phate, pyrophosphate, silicate, stearate. sulfide, and undecylenate. Zinc compounds are widely used in industry (refining, metallurgy, chemistry, textiles, electronics, wood products) and in medicine (deodorant, astringent, antiseptic, fungicide, and protective . in skin disease). Several organic Zn products are widely used in cosmetics, soaps, shampoos, toiletries 1 and patent medicines as bactericides and fungicides. Several important Zn com- pounds decompose under the action of water and air; these include the nitrite, permanganate. peroxide, phosphide, selenite, sulfide, sulfite, and telluride. It is of the utmost importance to remember that soluble Zn compounds may be convened to the insoluble carbonate, carbonate hydroxide, hydroxide, phosphate, pyrophosphate, silicate, or sulfide (which slowly oxidizes to the soluble sulfate) once they have been spilled in water. Toxicity: Local - Nonirritating except as follows: acetate, chloride, ethyls ulfate, forrnate. permanganate, and sulfate. Systemic - Low, except when the Zn is combined with such toxic components as arsenate, cyanide, phosphide, selenide, etc. Aquatic - High, regardless of the presence of other toxic components. Much n re toxic to fauna than to flora. ------- ZINC COMItUNt)S (continued) Detection: Commercial kits an available for detection; sensitivity range is 01 - 10 ppn (1,4,6). Suppliers include Larnotte and Rack. there is also a presumptive test teb is interfered wilt by Cd, S n (fl), Pb, and As (UI). )&t 1 ml of sample with Z ml of 10% NaZSZO3 and I ml of ZM NH 4 CN and 5 nil of 04 002% dithitone in CC1 Positive result the C d 4 layer turns red. (1,4, possibly 6) ------- ZIRCON1UM SULFATS Zr(S0 4 )z or H 2 ZrO(S0 4 ) 2 Synonym: Disulfatozirconic acid. Description: White, crystalline solid that sinks and dissolves. Water solutions are acid to litmus. At ordinary temperatures, dilute solutions deposit a solid on standing; this solid, known as Hauserrs salt, is a rearrangement of the molecule with the addition of water. The more dilute the solution, the more rapid the deposition. Toxicity: Human - Low. Aquatic - Moderate. Detection: Treat suspect solids with boiling aqua regia to redissolve the Zr. Test for Zr ion as follows. Mix 2 ml of sample with 2 ml of concentrated HC1 and 2 ml of aqueous 1% Alir.arin solution. Positive result: red precipitate. (2, 5,6). ------- APPENDIX B CROSS INDEX TO APPENDIX A: DICTIONARY There are two kinds of entry in this Cross Iiviex: 1. A single name in capital letters. Example: “ACETIC ACID.” This means that there is a page in the Dictionary titled “ACETIC ACIZY’. The pages are arranged alphabetically: the Introduction to the Dictionary explains the system. 2. Two names, separated by a colon; the second is in capital letters. Example: Acetic acid amine: ACETAMIDE. ” This means that information about acetic acid amine is on the page titled TM ACETAMIDE.” This Cross Index includes all the page titles of the Dictionary and all the synonyms. S-i ------- ABIETIC ACID ADS Detergents: ABI IC SURFACTAWfl AC: ALLY!. CELC*IDE AanwayDt aaniuns A TAMILIDE ACETIC ACID Acetic acid nine: ACETANIDZ Acetic acid a aiia salt: NaNiltal ACETATE Acetic acid butyl ester: BUrfl . ACETATE Acetic aldebyd.: ACETALDEHYDE ric pjnrrnnog Acetic oxide: ACETIC ANHYDRIDE Acetoethy lene: VINYL ACET&TE MflONE CYAJ4OSYDRIN AC ETOWZ T H ILZ Ac.tylb.rttene: ACfltPflflhE Mst BRONIOt Afl At.tyl.noq.n: CALCIWI CARBIDE Acetyl oxIde: ACETIC ANHYOPIPE Acid aodi s phosphate: SOCImI PW*PWtTt L a ID Xfl ACDYUC ACID Acrylic acid n—butyl ester: BUflL ACATIATE Acrylic_acid ethyl ester: JCTNYL ACHYLATE Acrylic resin nonr: NEnrtnCRnan acnzwxnns ADDIC ACID ADIP IflILE Adipyl. dinitrile: ADIP fl*ILS AIb : HYfS PEROXIDE Aldehyde: ACtThLD YDE Aldehyde ccli idene: rurz.n’sn PYRIDI IIE Aldebydine: nzxaThtL PYRIDINE Aldifen: DINIflCPR L Alkaryl sulfocates: ANIOUC stwncnwn Aflyl a z -fl a nium halides: QUATERNARY AIQCNI UN SALTS Alkyl benzene sulfonates: A NIOHIC SU*FACTANTS Allcaaleic acid: FUP%RIC ACID ALLYL ALCOHOL ALLYL CHLORIDE Altnini.a borate BORIC ACID ALZflIINIW FLUORiDE ALWUNUI4 SULFATE Aliairna trifluoride: ALImINUN FLUORIDE A1u qenste: ALUKINUN SULFATE A*Chlor: AJ10N1tTh4 CHLORIDE Azinoben ten.: MU Li NE At nctut.sn*: DUTYLAMI NE Aainoethane: ETHYLAMINE Asirsosthsn*1: NONOEttMANOLAMINE AMINO ETHYL ETHANOL AMINE LaS r ou,ethane: KETHY LAN! NE Arinonaphtbslene: *APHTHY LAN! NE Annophen: ANILINE Asinopropane: PROPYLAM! NE Minopropanol: 10001 SOflOPAMOLANI NE Aninotoluebe: S 4IY1AMINE and tOI.U IDENE AIS4(WIA A aAa crystal: A IV4ONIUN CARBONATE Lania gas: AItIOtIIA Asonia household: AlaON1A Awnia liquefied: AflCNIA ASfl AcETATE Aaniia bichroaate: £15011 1 DICHRC TE Amonjia bisulfide: A154ONIUM SULFIDE Lania borate: BORIC ACID Anita carbazotate: AIIOIUN PICEATE APII ItDI ARflJATE AsOInPc CHLORIDE AISSfl flfl Aaoni a cbnaste, neutral: ns nm CHStOnMt naitm DI cERONATE Amonia disulfatonicke late: flan NIOLI Lfl4 SULFATE ASt*It.P1 FEPaICYANIDE AD-AN B— 2 ------- AMMONIUM FERROCYAN IDE A nium hexacyanoferrate (III): AJ t NflN FERRICYANIDE Ammonitn hydrosuluide: AI4MONIUM SULFIDE A ni n hydroxide: AIOCNIA ? wnium uriate: AMMONIUM CHLOR IDE A niuru nickel sulfate: NICKEL APO IONIUM SULFATE AMPCNIUM NITRATE A?QVNIUM PICRATE Antoni4nu picronitrate: A IYSONILIM PICRATE MQON ION PEW HLORATE A1*ONIUN PEROXYDISULFATE Az wni.a persulfate: APGEWI IUM PEROXYDISULFATE APS ONIUM PHOSPHATE A oniwm phosphate, monobasic: APQIONILRI PHOSPHATE Ansonirin phosphate. primary: AIBIONIUM PHOSPHATE Awniwt phosphate, secondary: AW$ON ION PHOSPHATE A ni rhodanide: AMW)NIUM THIOCYANATE A nitw sesquicarbonate: AISION ION CARBONATE A1 NIWI SULFATE AIt ONItflI SULFIDE Anwrnita sulfocyanate: A*4ON ION THUCYANATE Aronitsi sulfocyanide APWONIW4 THIOCThNATE APION JUN THIOCYANATE AMYL ACETATE AMyl. acetic ester: ANYL ACETATE Awl alcohol: PENTANOL A l aldehyde: PENTANAL Awl carbinol: HEXANOL Asylene: PENTENE Amylene hydrate: PENTANOL A I hydride: PENTANE Anglesita: LEAD SULFATE Anhydrous an n is: AMMONIA ANILINE Anionic detergents: ANIONIC SURFACTANTS Antifreeze: ETHYLENE GLYCOL Antiscnous chloride: ANTIMONY TRICHLORIDE Antiaonous fluoride: ANTIMONY TRIFLX)RI bE Antimony chloride: ANTIMONY TRICHLORIDE Antimony compounds, soluble: ANTIMONY POTASSIUM TARTRATE Antimony fluoride: ANTIMONY TRIFLUORIDE Antimony oxide: ANTIMONY TRIOXIDE ANTIMONY POTASSIUM TARTRATE ANTIMONY TRICHLOR IDE ANTIMONY TRIFLUORIDE ANTIMONY TRIOXIDE Antimony white: ANTIMONY TRIOXIDE AP: A1S$ONIUN PERCHLORATE APC AI4ONIUM PERCHLORATE Aqua fortis: N iTRIC ACID Aqua regis: NITRIC ACID Artificial oil of ants: FURFURA.L Asphalt: PETROLEUM PRODUCTS, HEAVY Atabrine: QUINACRINE HYDROCHLORIDE Auro: NEUTRAL SURFACTANTS Azaanthracene: ACRIDINE Azacyclopropane: ETHYLENEIMINE Atiridine: ETHYLENEIMINE Azotic acid: NITRIC ACID AM -At 8-3 ------- Banana oil; AMYL ACETATE BARIUM CHLORIDE Baritw coapounds, soluble: BARIUM CHLORIDE BARIUM CYARIDE Bariun hydrate: BARIUM HYDROXIDE BARIUM HYDROXIDE BARIUM NITRATE Battery acid: SULFURIC ACID Bensalkcnita chloride: QUATER IIART A}CN 1DM SALTS Betas lkonia detergents; (JUATERNART AJQION 1DM SALTS Benaz ins: QUINOLINE 8 m m Benzene carbony]. chloride: BDJZOYL CHLORIDE BenzefleCarbOXYIiC acid: B SIZOIC ACID Benzst*diOl RYDROQUINtSJE, pnoCATUOL & RESORCINOL MnaenetriO l PY IWGALLOL $sninofonn: CARBON TETRACIELC*IDE Bsnoate of soda: BEflOIC ACID Bensoates: BENSOIC ACID BEN ZOIC ACID Benrol: BESZENE BEN ION IflILE aensopyridine: QUINOLINE Bensopyrrole 1 10012 Benoqui none: QUINONE B IXOYL CHLORIDE BEUTIaMIWE BERYLLIUM SALTS Bic&rburetted hydrogen: Bichtoeate of soda: Sa )ItJM D 1C BROSU iTE Bis (chioroethyl) sulfide; CARD as Blackstxap: MOLASSES Blue copperas; COPPER SULFATE Blue stone: COPPER SULFATE Blue vitriol: COPPER SULFATE Boletic acid: FtR9RIC ACID Boracic acid! BORIC ACID BORANES Berates, soluble: BORIC ACID Borax; BORIC ACID BORIC ACID Boron hydrides: BORANES Broucethylefle: VINYL BROMIDE BROMINE Bro mine cyanide; CYANOCEN BROMIDE Butane: PETROLEUX PRODUCTS, LIGHT Butanedicarboxylic acid: ADIPIC ACID Butanediol BUTYLENE GLYCOL. Butanethiol: BUTYL MERCAPTAN Butanol: BUTYL ALCOHOL Butenal: CROTON ALDEH Y DE Trans buteflediOiC acid: FUMARIC ACID Butcxyethanol ETHYLENE GLYCOL MONOBUTYL ETHER Butter of antimon y! ANTIMONY TRICHLORIDE Bunt AcET*TE WJTYL ACRYLATE W’TYL ALCOHOL BUTYLAM IKE Butyl cellesolve: ETHYLENE caa ICHOBUm ETHER BUTYLO IE GLYCOL Buty]. ethanoate: BUTYL ACETATE wm NERCAPTAN Butyl phthalate DIBUTYL P BTHALATE BA-SD B- 4 ------- CM.3MIUM CHLORIDE Cadmium compounds, soluble: CADMIUM CHLORIDE CADMIUM NITRATE CADMIUM SULFATE Cake alum: ALUMINUM SULFATE Calcium borate: BORIC ACID CALCIUM CARBIDE CALCIUM CYANIDE CALCIUM BTPOCHLORITE Calcium orychioride: CALCIUM HYPOCHLORITE CALCIUM PHOSPHIDE Caporit: CALCIUM HYPOCHLORITE Capryl alcohol: OCTYL ALCOHOL Carbamic nit.rile: CYANMIIDE Carbide: CALCIUM CARBIDE Carbinol: METHANOL Carbodiimide: CYANAMIDE Carbolic acid; PHENOL Carbon bisulfide: CARBON DISULFIDE Carbon chloride: CARBON TETHACKLOR I DE CARBON DISULFIDE CARBON MONOXIDE Carbon oxychloride: PHOSGENE CARBON TETRACHLORIDE Carbonyl chloride: PHOSCENE Carboxybenzene: BENZOIC ACID Catechol: PYROCATECHOL Cationic detergents: QUATERNARY A)QVJWIWI SALTS Cationic surfactants: QUATERNARY AIOCNIUM SALTS Caustic ant Sony: ANTIMONY TRICELORIDE Caustic baryta: BARIUM HYDROXIDE Caustic potash: POTASSIUM HYDROXIDE Caustic soda: SODIUM HYDROXIDE CetaUconiun halides: QUATERNARY AMPmNIUM SALTS Chameleon mineral: POTASSIUM PERMANGANATE Chinoleine: QUINOLINE Chinone: QUINONE Chloramine B: CBLOROAAINES Chiorsaine T: CHLOROAMINES Chioramines: CH&OROA ICNES CHLORIC ACID CHIfl Chlorine cyanide: CYANOGEN CHLORIDE CELOROACETIC ACID CELOROAMINES Chioroazotic acid: NITRIC ACID CIthOHOBEN Z EKE Chlorobenzol: CHLOROBENZENE CmnROBUTADI EKE Chloroepoxypropane: EPICHLOW)HYDRI$ Chioroethene; VINYL CHLORIDE Chloroethylene: VINYL CHLORIDE CHLOROFORM Chloroformyl chloride: PHOSGENE Chloronitrobenzene: NITROCHLOROBENZ ENS Chioronitrous acid: NITRIC ACID CULOROPLATINIC ACID Ch loroprene: CHLOROBUTADIENE Chloropropene: ALLYL CHLORIDE Ch loropropylene: ALLYL CHLORIDE CULOROSULFONIC ACID CHLOROTRIAZIDE C BLOROUS ACID Cinnasene: STYRENE Cinna 1: STYRENE Cisbutenedioic acid: MALEIC ACID Ciabutenedicic anbydride: MALE IC ANHYDRIDE Citrates: CITRIC ACID CITRIC ACID Coal naphtha BEN Z EN! Coaltar distillate: BENZfl4E Coaltar light oil: BENZENE Coaltar oil: BENZENE COBALT CHLORIDE Cobalt compounds soluble: COBALT CHLORIDE COBALT NITRATE COBALT SULFATE Cobaltous chloride; COBALT CHLORIDE CA—CO B-S ------- Cobaltous nitrate: COBALT NITRATE Cobaltous sulfate: COB LT sULFATE Colaaane: IIOImETRANOLAIIINE Coflunosol TRICRLOTCPHENOL Cologne Spirits: EThYL ALCOBOL Copper as: FERROUS SULFATE COPPER CW 4 tRIDS Copper coapounds. soluble COPPU. CELORIbE COPPER NITRATE COPPER SULFATE Corilagin: TANWIC ACID Corn sugar: GLUCOSE co n yr p Cre sa of tartar: BORIC ACID crasilic acid: PH OL CRE SDj. Crasylic acidt Cs.ESOL and nL CROT ALDEHYDE crotonjo aidehyda: Crystal awnia: A1004IUN cnnAn Cupfle chloride: COPPER CHLORIDE Cupric nitrate: COPPER * 17 5kfl Cupric sulfate: COPPER SUl FATE cwwa Cyanide of potash: POTASSIUM CYANIDE Cyanide of potsasis: POTASSiUM CYANIDE Cyancn’ic ACID Cyanoben tene t ZONITRILE CYANOWTADI E Cyanoetbylene: AcRYI 1TRLLLE Cyano enaj4e: CYAWI1IUE CflWOGEM BRIMIDE CYAW*ER CflORIDE Cyanogran: SODIUM CYANIOZ Cyanonethane: ACETONITRILE Cyanoprene: CYA ICBUThD tENt Cyclanon: NEUTRAL SURFACTANTS Cyc lo!iexañiened lone: QOINONE CYCWBmNE Cyclobexanecarboxylie acid: NAPnmnIIC ACID Cyclohexatriene: BENEENE Cyclopan: NEUTRAL SURYACTAN!PS CO-CY a-’ ------- Daran on : A)Q4ONIUM CHI RIDE DBP: DIBtITYL PHTRPL&TE DEA; DIETRANOLAMINE Decaborane: BORANES DEG: DIETHYIENE GLYCOL DEP: DIETHYL PHTRALATE Detergents; ANIONIC SURFACTANTS, NEUTRAL SURPACTANTS and QUATERNAJrf A14MONt 4 SALTS , anionic: - STJLFONATE Detergents, cationic: QUATERNALRY AMMON ION SALTS Dextrose GWCOSE Diamine: HYDRAZINE D IANINO E THaNE Diaminohexane - HEXAMETHYLENE DIAMINE D TAMYLA IUNE Diantimony trioxide: ANTIMONY TRIOXI bE Diazotizing salts; SODIUM NITRITh Dibasic sodium arsenate: SODIUM ARSENATE Dibasic sodium phosphate; SODIUM PHCSP RATE Dibenzopyridine: ACRIDINE Diborane: BORANES DIBUTYL PHTHALAtE DICHLOROBE U ZENP Dichioroethyl sulfide: MUSTARD GAS Dichlorodiethyl sulfide: MUSTARD GAS DXC ELOROE THANE D XC WIOROICTRANE DICELOROPHENOL DICELOROPROPANE Dicyanohutane; ADIPONITRILE Diesel fuel oil: PETROLEUM PRODUCTS, MEDIUM D IETHANOLAItINE DIETHYLAMINE Diethyl carbiriol: PENTANOL DISTHYLENE GLIYCOL Diethylolaaine: DIETHANOLAMINE DIETHYL PETRALATE Dihydroxybenrene: PYROCATECHOL and RESORCINOL Dihydroxybutane: BUTYLENE GLYCOL Dihydroxyd iethylanthe: DItF}ffiNOLAJ4XNL Dihydroxydietbyl ether; DIETHYLENE GLYCOL Dihydroxyethane: EThYLENE GLYCOL Dihydroxypropane: PROPYLENE GLYCOL Diisocyanatotoluene: TOWENE DI ISOCThNATE 0 IISOPROPANOLAMINS DIIS0PROPYt . I 1 . D IMETHYT.AMXNE Dimethylbenzene: Xut.ENE Dimethyl carhinol: PROPYL ALCOHOL Dimetbyleneimine: ETHYLENEIMINE Dimethyl ethyl carbinol: PENTANOL Dimethylpheno3: XYLENOL DIMETHYL SULFATE DIMETHYL SULFOXIC DINITROBENZENE Dinitrobenzol: DINITROBENZENE Dinitrogen monoxide NITROUS OXIDE DIN XTROPRENOL DIPA: D1ISOPRDPAflOLNIINE Dipentylain.ine: DIAMYLM4INE Disodium arsenate: SODIUM ARSENATE Disodialibutylphenylpheno idi— sulfonate: ANIONIC SURPACTANTS Disodium phosphate; SODIUM PHOSPHATE Disulfatozirconic acid: ZIRCONIUM SULFATE Disulfur dichloride: SULFUR CHLORIDE DMA: DIMETHYLAMINE DM50: DIXETHYL SULFOXIDE Dowicide b: TRICHLOROPHENOL DA-DO B— i ------- Dowicids 2 aM 2a: fljCWh PE DupOr iol : wThNfl Dutch oil: DICW 1 ORO€T SAIE DO-DU B-S ------- Edetates: Ethylene broaide: ETHYLENEDIAMINETETRa- VINYL BRCMIDE ACETIC ACID Ethylene chloride: EDTA: ETHYLENEDIA JINE- DIC1fl OROETNM(E and VINYL TETRAACETIC ACID CHLORIDE Elayl: ETHYLENE ETHYLENE CYANOHYDRIN Enanthyl alcohol: Ethylene&ianine: HEPTANOL DIA I4INOETHANE Engraver’ s acid: ETHYLENEDIAJ IINETETRAACETIC NITRiC ACID ACID EPICHLOROHTDRIN Ethylene dicarboxylic acid: Epoxypropane: MALEIC ACID PROPYLENE OXIDE Trans-ethylenedicarboxylic flinitrit: SODIUM acid: FUMARIC ACID NITRITE Ethy lenedinitrilotetraacetic Ethanal: ACETALDEBYDE acid: ETHYLEVVPIANINE- Ethananide: ACETAMIDE TETRAACET1C ACID Ethanedioic acid: ETHYLENE GLYCOL OXAL1C ACID ETHYLENE GLYCOL DIACETATE Ethanediol: ETHYLENE ETHYLENE GLYCOL NDNONJTYL CLYCOL ETHER Ethanenitr i le: ETHYLENEIMINE ACr ION XTRILE Ethyl hydroxide: ETHYL ALCOHOL Ethanodiaaine: Ethylic alcohol: ETHYL ALCOHOL DIAMINOETBANE Ethylidene chloride: Ethanoic acid: DICHLOROETHANE ACETIC ACID Ethyl phtha late: DISTHYL Ethanol: ETHYL ALCOHOL PHTBALATE Ethanolanine: Ethyl picoline: METBYLETHYL MCNIOETHANOLANINE PYRIDINE Ithene: ETHYLENE Ethylpropanol: PENTANOL Ether in: ETHYLENE Ethyne: ACETYLENE Ethine: ACETYLENE Eunatrol: SODIUM OLEATE ETHYL ACRYLATE Exiteli te: ANTIMONY TRIOXIDE ETHYL ALCOHOL Ethylaldebyde: ACETAIIDEHYDE rHYIfl ITHYLBEN IENE Ethyl benzol: ETHYL BEN SENt ETHYS Ethylene acetate: VINYL ACETATE Ethylene alcohol ETHYLENE GLYCOL Ethylenebisiminodiacetic acid: s Tx Yi. K P U K DIAMINE TETRAACETIC ACID B— 9 ------- Factitious air: NITROCS OXiDE Persentation alcohol: ETHYL ALCOHOL PERRIC CHLORIDE Peale hydrate: PERRIC HYDROXIDE PERRIC HYDROX IDE Perrie okide (hydrated): FERRIC HYDROXfl Ferric perch Joride: FERRIC CHLORIDE Lerric tesquisulfate: FERRIC SULFATE PERRIC SULFATE tactic tricMoride: FERRIC CHLORIDE Perrit trisultate: FERRIC SULFATE FERROUS HYDROXIDE FERROUS SULFATE FERROUS SULFITE Plores aartis EERRIC CHLORIDE Fluorocid: SODIUM FLUORIDE F1c tars of antinvny: ANTIMONY T HIOXIDE Flura-Orops SODIUM FLUORIDE FLUORINE FORMALDEHYDE Porn un: PORWLDEHYDE FORMIC ACID Forsic aldebyde: FORMALDEHYDE Porwl: FORMALDEHYDE Foraonitrile: HYDROCYANIC ACID Forayl chloride: CHLOROFORM Porayl trithloride C HLOROFORM FRUCTOSE Fruit sugar: FRUCTOSE FUMARIC ACID Fuaigrain: A YLONITRILE Fur aldehyde: FURFURA L Furane carbinol: PURPIJBYL ALCOHOL Furanedione; MALEIC ANBYDRIDE FURY URAL Purfuralcohol: FURFURYL ALCOHOL FURFITRYL ALCOHOL Furyl carbinol: FURFURYL ALCOHOL Pyrex: N4J4ON IUM PHOSPHATE PA- f l B-ID ------- GALLIC ACID Gailotannic acid: TANNIC ACID Gallotannin: TANWIC ACID Gardenal: PRENOBARBITAL Gardinol detergents: NEUTRAL SUflACTANTS Gaseous hydrocarbons: PETROLEUM PRODUCTS, LIGHT Gasoline: PE T RQLEtW PRODUCTS, LIGHT Glacial acetic dcidt ACETIC ACID Glucitol: SORBITOL GLUCONIC ACID GLUCOSE Glycerine: GLYCEROL GLYCEROL G 1vcocenit a:id (ç, ( Glycol cyar: :v. : ETHYLENE CYANOHYDR!W Glycol diacetate: ETHYLENE GLYCOL DIACETATE Glyconic acid: GLUCOI4IC ACID Glycy3. alcohol: GLYCEROL Grain alcohol: flHTh AlCOHOL Grape sugar: CLUCOSbI Green quinhydror -: ($JINHYDRONE Green vitriol: FERROUS SULFATE Gulitol: SORBITOL GA—GD B- il ------- Rartaborn: fl CARB TE t : PWSTAS) ( S Heavy carburetted hydrogen: Heavy greases: PETROLEUM Pfl?UCTS,EEAVT Septyl alcohol ‘ThNOL Hepty]. carbino]: OCTYL Denhydric alcohol: SORRITOL Denhydrobensene CYcLO N EXA N E Berahydrobentoic acid: RAPETBENIC C Pa ,tethy1en .: CYcIA I WZANE HEnnrRtIaIE DIA*Da aranaphthen.: CYCWHEflNE He nna PITROLEtS PRODUCTS, UGH? Deane diaaine: H E U IIETRYLD IE DIANINE flennedioic acid: ADIPIC ACID Rezone: NETDYLISOWTYL ZET(SE Rezyl alcohol: HEXANOL Nfl: CALCIUM HYPOCHWRXTT and BYPOCHWROUS ACID Rydracrylonitrile: ETHYLENE HYDRAZINE nowrmaxc acm HYDROCflRIC ACID HYDROFLUORIC ACID Hydrogen_carboxylic acid: Pcs)aC ACID Hydrogen chloride: HYDROenORIC ACID Hydrogen cyanaalde: CYWNIDE Hydrogen cyanide: HYDROCTANIC ACID Hydrogen dioxide: HTDRO N PENOXIDE HYDROGEN PEROXIUf Hydrogen sulfate: SULFURIC ACID Rydroqui.nol: HYDROcA J INONE HYDROQUINONE Bydrozybenxaldehyde: SALIC Y LALDEHYDE flydrorybensene: PHENOL HydroxybenzOic acid: SALICYLIC ACiD Hydrozycarballylic acid: crrRzC ac m Hydroxydimethylbenrene: XTLEROL Hydroxydinitrobenflne: DINI 1 PU E 3L Hydroxyethylasine: NONOETHANOLAJ4INE his (Rydroxyethyl) swine: DIETHANOLAMI N E Rydroxyethylethylenedia*int: AMINO ETHYL ETHANOl. AMINE Hydroxyheptane: HEPTA*)L Hydr oxyi sobatyroni t n 1 .: kczlva CYMIOHYDRIN uYDRomPaINE nydroxyaethylfuran: F’URFURYL ALCOHOL RydroxynaPbthaltfle NMRTHOL Hydroxyphenol: RESO INOL Hydroxypropanetricarboxylic acid: CITRIC ACID ffintrarvtrooanoic acid t - - LACTIC ACID Hydroxypropionitrile: ETHYLENE CYMIOHYDRIN Hydroxypropylaaine: psoHots R oPANOIAPCNE Bydroxytoluene: CRESOL ifypaone : ACE IOPHENONE HyPOtRI.OWXIS ACID Hyponitrous anhydride: NITROUS OXIDE HA - WY 8-12 ------- Iminodiethanol: DIETHANOLAMINE INDOLE Iron chloride: FERRIC CHLORIDE Iron hydrate: FERRIC HYDROXIDE Iron hydroxide: FERRIC HYDROXIDE and FERROUS HYDROXIDE Iron oxide (hydrated); FERRIC HYDROXIDE Iron perchloride: FERRIC CHLORIDE Iron persuifate: FERRIC SULFATE Iron sulfate: YER.RIC SULFATE and FERROUS SULFATE Iron tersulfate: FERRIC SULFATE Iron trichioride: FERRIC CHLORIDE Iron vitriol: FERROUS SULFATE Isoantyl acetate: AMYL ACETATE ZSOPRENE Isopropanol: PROPYL ALCOHOL Isopropylacetone: METHYLISOBUTYL KETONE Isopropyl alcohol: PW)PYTL ALCOHOL Isovaleral; PENTANAt Isovaleraldehyde: PENTANAL Isovaleric aldehyde; PENTANAL Iriur: NEUTRAL SURFACTANTS IM-IR 8-i 3 ------- Jet fuels; PETROLEtM panTS , 33 -n 8- 14 ------- Raridir; SODIUM FLUORIDE Kerosine: PETROLEUM PRODUCTS, MSDI1 4 n-XE s-15 ------- LACTIC ACID LACTOSE Lanarkite: LEAD SULFA T E IANTEAfl ACETATE laughing gas: NIYI )US OXIDE ____ LavaCOl ETHYL ALCO8OL LEAD ACETATE LEAD ARS A7X LEAD CHLORiDE LEAD NITRATE Lead orthoar senate: LEAD MSE TZ LEAD SULFATE LEAD TETRASTRYL LmiioOl in.: QUI IIOLINE LavulOast FRtCTOSE Lichenic acid: Ftlu.RIC ACID Light solvents: pETROLEUM pwiNCfl. LIcr Ligroint PETW)LflI PROOtETS LIGHT LINOLSIC ACID Linolic acid: LINOLEIC ACID Linseed oil; LINOLEIC ACID Liquefied gases: PETROLEUM PIt000CTS • LiGHT Lissapol; NEUTRAL SDRPACTMTS LITHItM CHLORIDE Losa ntin; CAWIWI HypOC HLORITE Lu icants: PETROLflM p )OUCtS • HEAVY Lubricating oils: PETROLfl PRODUCTS • Nfl)IiP Lisinal: PHUIOBAR3I T AL Lye: POTASSItM HYDROXIDE and soo ItRI HYDROXIDE Lysol: OtESOL la-LY B- 36 ------- MALEIC ACID MALE IC ANHYDRIDE Maleinic acid: MA.LEIC ACID Platonic nitrite: CYANOACETIC ACID Maltobiose: MALTOSE MALTOSE Malt sugar: MALTOSE MCA: CHLORACETIC ACID PlEA: MONOETHANOL.A IIINE MEP: METHYLETHYL PYRIDINE Mercaptoacetic acid: THIOGI.YCOLIC ACID Mercaptomethane: METMANETH IOL Me thana 1: FORMALDEHYDE METHANETHIOL Methanoic acid: FORMIC ACID METHANOL METHYL ACETATE Methylacetic acid: PROPANOIC ACID Methylacetic anhydride: PROPANOIC ANHYDR1DE Methylacrolein: CROTONALDEHYDE METHYL ACRYLATE Methyl alcohol: METHANOL METHYLAMI NE Methyl aniyl carbinol: HEPThNOL Methylaniline: TOLUIDINE METHYL AZIDE Methylbentefle: TOLUENE Methyl butadiene: ISOPRENE Methylbutanol: PrANOL Methylbutyl alcohol: PENTANOL Methylbutyraldehyde: PENTANAL Methyl carbinol: ETHYL ALCOHOL Methyl cyanide: ACETONITRILE Methylene chloride: D1CHLOROKETHANE Methylene dichloride: DICKLORW IET H ANE Methylethylene glycol: PROPYLENE GLYCOL Methylethylethylene PENTENE METHYLETHYL PYRI DINE Methyl glycol: PROPYLENE GLYCOL Methythexyl carbinol: OCT11 ALCOHOL METHYL ISOBUTYL XE1VNE Met y ljactonitrile: ACETONE CYANOHYDR I N Methyl mercaptan: METHANETHIOL METHYLJ4ETHACRYLATE Methylnitrophenol: NITROCRESOL Methylpentanone: METHYLISOBUTIL KETONE Methylphenol: CRESOL Methyl propenoate: METHYL ACRYLATE Methyl propyl carbinol: ?flCANOL Methyl sulfhydratc: METHANETHIOL Methyl sulfoxide: DIMETRYL SULFOXIDE Mcthyltoluene: XYLENE Methyl trichloride: CHLOROFORM MIBK: METHYLISOBOTYL KETONE Milk acid: LACTIC ACID Milk sugar: LACTOSE M I PA: MONOI$OPROPANOL MIINE Mixed acid: NITRIC ACID Modinal: NEUTRAL SURFACTANTS MOLASSES Molybdenum trioxide: MOLYBDIC ANHYDR IDE Molybdic acid anhydride: MOLYBDIC AXHYDRIDE MOLYBDIC ANBYDRIDE Molybdic oxide: MOLYBDIC ANEYDRIDE Monobasic sodium phosphate: SODIUM PHOSPHATE .Monochloroacetic acid: CELORCACETIC ACID MOIOETHAJJOI.AMINE Monoethylaai-ne: ETHYLAMINE MONO ISOPROPANOLAMI NE Monoaethylanine: MtTHYLAMINE Mononitrogen nonoxide: NITRIC OXIDE Moprof ix: NEUTRAL SURFACTANTS Moringine: BENZYLAMIN! P4uriatic acid: HYDROCHLORIC ACID MUSTARD GAS MA-MU S-li ------- Nacconate: TC)LUXNE NITROPEENOL DIISOCYANATE NITROPROPANE PHTEALD IE NITRWS ACID NaphtMlene dicarboxylic acid NITROUS OXIDE NAnT H ALm Nitroxylefle: NITROXYLOL )ThPHTHALIC ACID NITROXYIJOL Mapbthalidine NAPUTH ILA I IINE n-tctyl sodiua sulfate: NapthaIin NnHTHAI.ENE NEUTRAL SURPACTANTS Kaphthene: HAPHTHALflIE Normal sodium pyrophosphate NAPHTH IIC ACID SOD 113)3 PHOSPHATE NAPHTW)L Norway saltpeter: ,aPHTHYIANINE AMNONIW4 NITRATE Natri ls: SODIUM Nutgall extract: TANNIC ACID Neutral potassium chromate; POTASSiUM CURCIaTE Neutral sodium chromate: SODIUM CHROIthTE Neutral spirits: ETHYL M 08OL NEUTRAL SURFACTANTS NICKEL AJISONI IBI SULFATE NICKEL CHLORIDE NICKEL NITRATE Nickelous chloride: NICKEL CHLORIDE Nickelous nitrate: NICW. NITRATE Nicks bus sulfate: NICKEL SULFATE NICKEL SULFATE Witran hline: NITROANILINE Nitrate of annia: ASONI IPI NITRATE Nitrating acid: NITRIC ACID NITRIC ACID NITRIC OXIDE NITROANILINE NITROBENEKIE Nitrobentol: NITROBENE ENE mR0CHLOROBEflENE NITRCXRESOL NITRCGEN DIOXIDE Nitrogen monoxide: NITRIC OXIDE NITROGEN TETROXIDE Nitrohydrochioric acid: NITRIC ACID Nhtrcauriatic acid: NITRIC ACID NA-NU B- 18 ------- Octadecandienoic acid: LINOLEIC ACID Octadecenoic acid: OLEIC ACID Octanol: OCTYL ALCOHOL OCTYL ALCOHOL n-Octyl sodium sulfate: NEUTRAL SURPACTANTS Odpn: OXYPROPIONITRILE Oil of mirbane: NITROSENZnm Oil of vitriol: SULFURIC ACID Olefiant gas: ETHYLENE OLIEIC ACID Oleic acid sodium salt: SODIUM OLEATE Ole u m: SULFURIC ACID OXALIC ACID Oxannonitus: HYDROXYLANINE Oxydiethanol: DIETHYIflE GLYCOL Oxyme thy lene: FORMALDEHYDE OXYPROPIONITRIIS OC-OX 5-19 ------- Pandthydroxyben zone: HYDROQutNO , Paraforv: PARAPOR1 LDEHYDE PAnFORIaIaEHYDE Pars ldebyde: ACEThLDEHYDE Paste waxes: PETROLEtM PROO(CTS, E VY Patent aji : ALWUNUM SULFATE Pear oil: AMYL ACETATE Pentacetate: MIYL ACETATE PMUTAfl PentaedieneonS t n It: PUftA$OL Pentanol •cttate AMYL ACETATE fl it ” ’ PERCELORIC ACID Perctloro.ethanst c*now TRTPAcRLORIDE Perch loron: CAiCI Oil HYPO— CHL Ifl sad HYPOcKLOROUS ACID Peroxide: HYDROGEN PEROXIDE nna au z PEflOLE 1JI PROCUCTS, PSTHQLEIII PRODUCTS m n n icn , Phase: BflIfllE Pliezic iot a: PHENOL PHENOBARBITAL Phenctaxti tone: P O5ARBITAt PRNmL S-Pbenplac.taaide: flNtLIDE flseayl saint: PJ(ILIJZ PbenyTharbitunic acid: PHfl SARBITAL nmz.aar.axxwz CEI IDE Ptteayl chloride: CUW& Pttenyl cyanide:_BflZONI’TRILE Pbeaylethaae: nun BENSENE Theny lethy lent: STYREfl itenylforaic acid; BZOIC ACID Theny l hydride: Bfl Itenylic acid: PHflW. Pttenyinethane: DOLUEPJE Ptkenyinetby larine B ZYLAM I KE Phenyl ethy1 ketone: ACETOPW JOWE PEOSGE JJ I PHOSPHOR iC ACID Phosphoric sulfide: PHOSPHORUS PENTASULE IDE PHOSP HORUS Phosphorus chloride: PHOSPHORUS TRICKLORIDE PHOSPHORUS OXYCELORI DE PHOSPHORUS PENTASULF IDE Phosphorus persulfide: PHOSPHORUS PENTASULF IDE PHOSPHORUS TRICKLORI DE Phosphoryl chloride: PHOSPHORUS OXYCKLORI DE Photcphor: CALCI%N4 PHOSPHIDE Fhtha llc acid dibutyl ester: DIBUtYL PUTHALATE Platinic chloride: CHWROPLATINIC ACID Polyether glycol: POLYGLYCOL EtHER POLYGLYIDL ETHER Potash hydrate: POTASSIUM HYDROXIDE ?ot.eaPiua antiaonyi tartrate: ANT 110 ( 7 POTASS I !S4 ¶ARTRME Potassits bidtroaate: POTASSIUM DIO IROMATE Potassius borotartrate BORIC ACID POTASSItHi CHRC*IA’tE POTASSIUM CYANIDE POTASSIa . DIC IIROMATE PC’TASSItIl HYDROXIDE POTASS lull PERMANGANATE Proof spirits: E YL ALCOHOL PHOPANAL Propane: PZT )LE&PI PRODUCTS 1 LIGHT Propanediol: PROPYLENE GLYCOL Propanetziol; GLYCEROL PROPANOIC ACID PROPANOIC ANHYDRIDE HEAVY L iGHT leblifli PA -PR B -20 ------- Propanol: PROPYL MCOHOL Propenenitrile: ACRYLONITRILE Propenoic acid: ACRYLIC ACID Propenol: ALLYL ALCOHOL Propane oxide: PW)PYLENE OXIDE Propenyl alcohol: ALLYL ALCOHOL Propionaldehyde: PROPANAL Propionic acid: P R OPANOIC ACID Prop ionic a idettyde: PROPMUIL Propionic arthydride : PROPANOIC ARHYDRI bE PROPYL ALCOHOl t Propyl aldehyde: PROPANAL PROPYLAMINE Propylene dichioride: DICHLOROPROPANE PROP YLmm GLYCOL PROPYLfl(E OXIDE Propylethylent: PENTDIE Prussic acid: HYDROCYANIC ACID PYRIDINE Pyrocatechin: PYROCATECHOL PYROCATEC HO t Pyrogallic acid: PYROGALLGL PTROG&LLOL Pyronucic aldehyde: PURPURAL PR - f l B -2 1 ------- Quaternary aaines: QOATERNARY AJO4Ct4IUM SALTS QUAT NARY A1QI)NIUM SALTS p cRJflE HYDROCHLO I DE QU IN ar URO NE Qoinidine: QUININE QUIND Qoino]: HYDROQUINONE QUE IOLDIB cPINOKE QUA -QU I B- 22 ------- Red oil: ANILINE and TOLUENE Red potassiun chronate: POT?. SSIUY ‘ ICHROMWFE Red prussia socf : SODIUM FERRICYANIDE Residual fuel oil: PETROLEU]4 PRODUCTS, HEAVY Resorcin: rZSflhCI Ot RESORCINOL Road oil: PETROLEUM PRODUCTS, HEAVY Roccal: DIKET I4YLRENZYLAM1IONIUM CHLORIDE arsc )UtTERNARY P_’!11flNT .Th c r ’iq RE-RU 8-23 ------- Safflower oil: Sodina bisuifide: LIW IEIC ACID SObl1* HYDROsULYIt Sacchara lactis: 500 1W! MSULYITE LACTOSE Sodlia borate: SOflC ACID Sa l. oniac: MM0WTW so fiia broaobenzene su lfonate: cUWR.WE ANIOWIC SURFACTANfl Sal eMlybdis: FERROUS Sodit aetylate: SODIW! WI2ATE PA IXITATE 5A1 4 1CY1,IC ACID Sodia chlorotbiazide; Salicylic aldebyde CHLo BTIA1IDE sALICrzawflYDE 500111! cHRoIan Sal icy ].al: sootti! CYMMtE SALICYLALDEHYDE 50o111! CYANIDE SIC. DEflDE sod4u* dscylbenene sul fonate: Salaiac: AIIIWILP I ANIONIC SURYACTANTS SodMa dichlorobenzefle sulfonatet San&pan: 1 ’XRAL ANIONIC SURYACTANTS WflAC?AW?S 5001W! DICBRC 4ATt Ssntasrse: ANItI IIC Sodits dinitrophenol: JRFACTANTS DINITROPHEROL Sardipan: rML Sodita dodecylbensene sulfonate: SDRYAC?A2ITS AN IONIC SUBPACTAWXS Saturated cyc oslkyl swnw 7 P1CflSU)Z fatty acids: HAPHT IC 500111! FSRROCYANIDE S W 1W ! PLUOPIDE Sodits fluorosilicate: Stlenii.a oo ounds: SODItI ! PWOSILICATE snaxw 50onm auoszwCAfl 5enart ntlte: sodiwu hnacyanoferrate (I ll): kjflxNray flIO*IDR 50011$! FflRlCflMlDt SThVfl Sodits hezacyanoferrate (II): Silver salt: ANIONIC nj njq pn jp WRYACTANTS Sod I a hexadecanoate: nan, c ncn soottis i’aucnn sumGE, DIGISTE ) SEWAGE Sodiis hexadecylate: SCZIIW( cAv a RAN VWIGEStV PAL N X T ATE UIMGE Sodits hydrate; )fl hI 5 0 0 1 W ! HYDROXIDE Sodia acid sulfite: Sodjus hydrogen sulfide: 5001 11K EISUIPITE SOOflJl WYD $UIZ1DE Sodsa anthraqinnone Sodia hydrogen sulfite: sulfonate: ANIONIC 500W4 SISULflTE WRFACThNTS $OtjIl$! ffYDROSULFIDE stflzm ARSmafl 50011$! HYDROXIDE 50011$! ASIDE Sodiia lauryl sulfate: Sodiia benzoate: c’rnz. t0IC ACID Sodiun aetabjstjlf its: Sits bicbrcsate: S fl1S BISCX.PIfl sanwi DIC flTE 5k-SO 3—24 ------- Sodium methoxide: SODIUM METHYLATE SODIUM METHYLATE Sodium monobutyldiphenyl sulfonate: ANIONIC SURFACTANTS Sodium nonobuty lphenyiphenol monosulfonate: AN IONIC SURFACTANTS Sodium znonosulfide: SODIUM SULFItE Sodium naphthalene sulfate: ANIONIC SURFACTAN?S SODIUM NITRITE 5 (4 nitroctUorobentene sulfonate: A Ii IONIC SURYACTANIS Sodium octadec noate: SODIUM STEARATE SODIUM OLEATE SODIUM PALMITATE SODIUM PHOSPHATE adiun prussiate yellow: SODIUM FERROCYANIDE Sodium rhodanate: SODIUM TM IOCThPATE Sodium rhodanide: SODIUM THIOCYANATE Sodium salts of sulfated fatty alcohols: NEUTRAL Sti RYACTANTS SCOItYM SILICATE Sodiwt silicoflunride: SODIUM FLUOSIL ICATE SODIUM STEARATE Sodium sulfhydrate: SODIUM HYDROSULFIDE SODIUM SULFIDE SODIUM SULFITE Sodiun sulfoanthroquinone; ANIONIC SURFACTANTS Sodium sul focyanate: SODIUM THIOCYANATE Sodium sulfocyanide: SODIUM THIOCYANATE Sodium sulfuret: SODIUM SULFIDE SODIUM THIOCYANATE SODIUM TUNGSTATE Sodium wolf ranate: SODIUM TUNGSTATE Sorbit: SORBITOL SORBITOL Spent sulfuric acid: SULFURIC ACID Spirit of Mindererus: A IOSMi IUM ACETATE Spirit of wine: CrISIL ALCOHOL S’rANNOUS CHLORIDE Starch syrup: GLUCOSE Stearic acid sodium salt: SODIUM STEARATE STRONTIUM CHLORIDE STRONTIUM NITRATE STYRflIE Styrol: STYRENE Styrolene: STYRENE Sugar of lead: LEAD ACETATE SULFUR CHLORIDE SULFUR DIOXIDE Sulfuric chiorohydrin: CHLOROSULFONIC ACID Su.fur monochioride; SULFUR CHLORIDE Sulfur mustard: MUSTARD GAS Sulfur subcbloride: SULFUR CHLORIDE SULFURIC ACID SULFUROUS ACID Sulfurous anhydride: SULFUR DIOXIDE Sulfur dioxide solution: SULFUROUS ACID Sulfurous oxide: SULFUR DIOXIDE Superoxol: HYDROGEN PEROXIDE SUPERPHOSPHATE Surf actants, anionic: DISODflMDIBUTYLPHENYLPHENOZr DISULFONATE Surfactants, cationic: QUATERNABY AWCNIW SALTS Sylvic acid: ABIETIC ACID SO —ST 5-25 ------- Tall oil: LINOLEIC ACID TA 1C ACID tannin: TANWIC AC 1!) Tar camphor: Tartar attic: PStDIO4T POTASSIIJ4 T&R IRA T E ‘?artaflzed Wtis ;.v AflZNo? / Pflt P?!$! TARTRAT3 Tartr*ted ant t ny: ANTDCWT POTASS Ia I TARTRATE TASP: SODIWI PHOSPHATE ! fl: TOLU DITScCYANATE TEA: TRIfl NQLAflIfl Taoqutnol: BYDR000].flE Taepo2: NtngAL S MYACTAn 1 A: TETRAZTUYIflE Pflrn’nw Tax-qavt?n ø?tt v;ac IRFACt1 VtS TETA: flL21WT2 1Wt1JJE Tttrachloroaetbane: CA n O N ?ETkACHLORIDE TSTRARflTLENE P TAMIfl Tetraethyl lead: LKAD TETRAPTEYL ?etrImc ’’v1a . . c 2. !e; ø’v Tetraaet_tiysene dicyanide: AD IPONITRILE t tra sodiun pyrophosflate: SCt3TUN PHOSPHATE Tta ll&ii O pounds: THALLIUM ?HiOG yeQIj ACID Thioq lycalflc acid: ?HTOGLYCOLIr ACIJ Thi ,methy1 alcr!,el: Thiophosphoric anhydride: PHOSPBOW3S P TASULflDE THQRfl q CRLOflDE Ta3Rns4 NITRATE rium tetrach lorjde THORIUM CHLOitIDE Tin crystals: STAN! QUs CfflAtrog Tin dichioride: STAMNOUS CHLORIDE Tin protochioriac: STANNOUS Ca ORIDE Tin salt: SThNWXJS CHLORIDE T I tcr’- ‘ flc’ounds? fltaNLtjP COlO ft)KD& TITANIUM C pc)tm,rE Ti tanous OO )ounds TITAN lU l l C WOUNDS Titanyl OOmpOUadS: TITAN IW I COMPOUNDS ThA : TRlMflRYzJs4Jja ycwm TOWENE D l ISOCYAXAt ? flUID I KE Toli l: TO1A ’ 131R Tiolylene £ tOU EN Lu 3 s:v Tbxiljc set - I: *A221C ACID Toxille sabydride: MALEXC ANHYDRIDE Tribasic sodiua phosphs SO(’7UM PHOSPhATE ir C &juzex: Tik ICaO?c.PHENOL Trtchloroaethane: CEIMROFORI4 7 ICjmca p xpj oy. TRIETHANOIAI I IW tRIEyHyIaniwj TRIETHYLENET TRAj4 pi Trihydroxybentene: PYRCXZXLLOL Tzibydrobenrosc acid: GALL 1C ACIL tlhydroryethylan4ne: TRIETWJIOLAMIIJE T RIMETHflaK IKE Thiaethyler 1 t. 1 r : PROPYLfla GLYCOL Triple tuperphosphate: SUPERPHOSPHATE Trisodiur arsenate: SODJIPI ARS TE TA-TR 3-26 ------- TSP?: SODIUM PHOSPHATE Turbine fuels: PrrRo flq PRODUCTS, MEDI1 I Turkey red oil: OLEIC ACID fl-TU 2—27 ------- Unrefined petroleta; PKTROL&JP(, cRUDE UN -UN ------- Valentinite: fl TIMONY TRIOXIDE Valeral: PENTANAL Valeraldehyde: PENTANAL Va]eric aldehyde: PE?CANAL Vanadic sulfate: )‘MADYL SUI3ATE Vanadium oxysulfate: VMaDYL SULFATE Vanadium sulfate: VANADYL SULFATE VANADYL SULFATE VC: VINYL CHLORIDE Ventox: ACRYLON 1TRILE Villiaumite: SODIUM FLUORIDE Vinegar: ACETIC ACID VINYL ACETATE Vinylacrylonitri Xe: CYANOBUTADIENE VINYL BROMIDE Vinyl carbinol: ALLYL ALCOHOL VINYL CHLORIDE Vinyl cyanide: ACRYLONITRILE Viny].formic acid: ACRYLIC ACiD VA-V I 2-29 ------- 1 ter glass: SODItPI SILICATE weisspiessglanr: ANTTht*JY mIOXIDE White caustic: SODIUM HYDROXIDE Wood alcohol: METHANOL Wood spirit: METHANOL 8-30 ------- XYLflth XYLENOL Zylols XYIENE n- f l B— 31 ------- Yellow prassiate of scda: SODIUM FERROCThNIDE YE—YE B- 32 ------- ZIN C CQM?oij!cs ZIRCONI SULFATE Zynafluor: SODIUM FLUORIDE fl —zr B-33 ------- APPENDIX C CATEGORIZATION OF HAZARDOUS POLLUTING SUBSTANCES The Categories There are seventeen categories: 1. Solid—soluble 2. Solid—insoluble—floats 3. Solid-insoluble-sinks 4. Liquid-miscible 5. Liquid—itriscible—floats 6. Liquid—imzniscible—sirtks 7. Gas These categories indicate whether the spill dissolves, or is visible on the sur- face or bottom. A fine powder may float or remain susp nded even if it is heavier than water. Applies if there was spill on the ground but no visible trace reftiains. The color of the bulk substance or a strong solution. 9. Fumes Observed only at time of spill or soon after. 10. Vigorous reaction 11. Odor—unpleasant 12. Odor-not unpleasant 13. Lacrimatory 14. Flammable On contact with water, rapid generation of gas, heat, noise, flami, explosion. Unpleasant odors are disagreeable even at low concentration. The others may be disagreeable at high concentration. Induce eye watering even at low concentration; many others do at high concentration. CAUTTONt test a small sample, well away from the spill. NOTES B. Color: red, yellow, green, blue, misc. c- i ------- 15.. Acid Giie a clear reaction 16. Alkaline (e.g., litwas red/blue) at low concentration. 17. troth Readily torn persistent froth. Using the Categorisation: (a) Observations APPLICABLE CATEGORIES Be alert for odor and lacrlt.ion when first a roaching the spill and throughout rsnfl 11 ,12,13 • Icok for solid or liquid in the water, and on the ground if spilled inshore. 1,2 ,3 , 4, 5 ,6 ,7 • Scot for abnormal color in the water, and on the ground if spilled inshore. S • Ask witnesses of the spill about fises and vigorous reaction. 9,10 - If a sasple of the spill can be collected from the watr surf or inshore, teat for fl 1Uity. If negative, try an i rovised wick, extra shelter from wind, etc. Test a a ma s 1a, Ct. AWAY f-rca the spill. 14 - test the water with 1i s paper - Check a reference sa l. of water from outside the spill zoom. 15,16 • If there is natural turbulence (rapids, falls), look for per— sistent froth; -if not, shake a s le in a glass container. Osct a refere s le of water from outside the spill room. 17 C—2 ------- Using the Ca gorization: (b)Eliaination • Note which categories apply to the observed properties of the spill. • Note Stitch substances appear in all or most of these categories. • Check the data for each of these substances in the Dictionary. • Determine which is the sst likely candidate. Apply confirmatory tests. If the identification is uncertain, test other candidates. flNIPLE; The spill is observed as a surface file of colorless liquid with an araatic hydrocarbon (benzene-like odor. Category S (Liquid- insoluble—floats) reduce the possibilities to 32. Category 1.2 (Odor-not unpleasant: bensenel reduces the possibilities to 5; bensene, ethyl benrene, styrene, toluene zylene. A cross- check with Category $ (Color) verifies that none of these S is colored. Category 14 (Flasasbility) shows bensene as highly flaahle the others less so; but this would not be decisive. The individual Dictionary entries show no definitive field test, but indicate that the properties of all five are sufficiently similar for damage investi- gation to proceed while positive identification is made at a permanent laboratory. Limitations • The substances are categorized according to their usual properties, but the spill may have an unusual color, smell, etc., due to i urities. A few substances are not listed at all, because their obvious characteristics are too variable or ill—defined. The physical state of the spill (solid/liquid/gas) say be different in cold or hot weather. Odor is difficult to describe and identify, and individual reactions vary widely. C-3 ------- Category 1: Solid- soluble Acetaznide AIkyl aryi ammanium ha l ide Mundaum sulfate Azntntnium compounds Antimony trifluoride Barium chloride Barium cyanide Berythwn chloride Beryllium nitrate Beryllium sulfate (hydrated) Borate. ftnost) tort- butyl alcohol Cadmt*mi chloride Cadndum MUst. Cadmium sulfate Calcium cyanide Chloroacetic acid Cbloroplatfnic acid Citric acid Cobalt chloride Cobalt nitrate Cobalt sulfate Copper chloride Copper nitrate Copper sulfate Cyanarnite Cyrnaretic acid Cyanogen bromide Diisopropanolaznine Perric chloride Ferric sulfa te (hydrated) Ferrous sulfate Fructose Gluten Hesam yleae diamine Lactose Lanthanum acetate Lead acetate Lead nitrate Lithium chloride tdaleic acid Maltose C — 4 ------- Nickel ammonium sulfate Nickel chloride Nickel nitrate Nickel sulfate Phenobarbital (sodium salt) Phosphoric acid Phosphorus pentasulfide (decomp.) Potassium hydroxide Pyrocatechol Pyrogallol Quinacrine hydrochloride Re sorcinol silver nitrate Sodium hydroxide Sodium salts (most) Sorbitol Stannous chloride (white sediments Stronttnn chloride Strontium nitrate Tanaic acid Thallium acetate Thorium chloride Thorium nitrate Vauady) sulfate Zinc chloride Zinc nitrate Zinc sulfate Zirconium sulfate c—s ------- Category 2: Solid-insoluble-floats (See note to Category 3..) Maleic anhydride Sodium (reacts violentlr products dissolve) C- 6 ------- Category 3: Solid-insoluble-sinks NOTE that sinking is the expected behavior of compact masses of the substance. Fine crystals or fluffy aggregates may float, or fine powders remain in suspension for a long time. Acetaaflide Ac r Hine Adipic acid Aluminum fluoride Anti mony trioxide Bensoic acid Beryllium sulfate (anhydrous) Calcium carbide (reacts) Calcium pbosphide (react.) Dichlorobensene (para-) Dicblo rophenol Ferric hydroxide Ferrous hydroxide Ferrous sulfite Fumaric acid Gallic acid Lead arsenate Lead chloride Lead sulfate Molybdic anhyd.ride Naphthalene Naphthaiic acid Naphthol Napbthylaxnine Nitroaniline Nit rocblorobenz ens Nitrocresol Nit rophenol Quinhydrone Quinine Quinone Salicy]ic acid Sodium fluosilicate Superphosphate Toluene diisocyaaate (reacts) Trichiorophenol c-7 ------- Category 4: Li uid.-miscible Acetaldebyde Acetic acid Acetic anhydride Acetone cyanohydrin Acetonitrile Acetyl bromide (decornp.) Acrylic acid Acrylonitrile Allyl alcohol Amino ethyl ethanol amine Benzylaznine Butylanilne I 3 -Butylene glycol Chloric acid Chlorosulfonic acid (reacts violently) Chlorous acid Cyanogen chloride D iantinoetha ne Diethanola ifline Diethylaxnine Diethylene glycol Dintethylamine (water solution) Dintethyl sultride Ethyl alcohol Ethylan i l ne Ethylene cyanohydrin Ethylene glycol Ethylene glycol diacetate Ethylene glycol nionobutyl ether Ethyleneimine FormaHehyde (water solution) Formic acid Furfuryl alcohol Glycerol Hydrasine Hydrochloric acid Hydrofluorit acid Hydrogen peroxide HypochlorouS acid Lactic acid Methanol Methyl acetate C-S ------- Mono ethanolarnine Monoisopropanolantne Nitric acid Nitrogen tetroxide (decomp.) Nitrous acid Oxydiproprionitrile Perchioric acid Phosphorous trichioride (decomp.) Polyglycol ether Propanal Propanoic acid Propyl alcohol Propylamine Propylene glycol Propylene oxide Pyridine Sulfur tblioride (reacts) Sulfuric acid Sulfurous acid Tetraetbyltne pentarnine Thioglycolic acid titanium tetrachia ride (reacts violently: sediment) Triethanolaminc triethylene tetrante tritnethylamine C —, ------- Category 5: Ligtñd-inuniaciMe-floats Ad iponitrile Ally! chloride n -Amy! acetate Beasene n-Duty! acetate fla Duty! acrylate Butyl alctls (eac. tefl-) Butyl mercaptan Crotonaldehyde Cycishnane D iamylarnine Dilsopropyismine (volatile) Ethyl acrylate Ethyl beasene Hna ol Isoprene Linoleic acid Methai dhiol (very volatile) Methyl acrylate Methylisobotyl ketone Methyl methacrylate Octyl a.tcoMl Oleic acid Pentanal Pentane (volat ile) Pentene (volatile) Petroleum crude and products Styrene Telnene Viny! acetate Zylene c -to ------- Category 6: Liq 44 -ixnndscib1e- sinks Carbon disulfide Carbon tetracklo ride Chlorobenzene Ch loro for m Dichioroetha i ne Dichiorometbane Dichioropropane Diethyl phthlate Epichiorobydrin Lead tetraethyl Mustard gas Hitrobenzene Nitroxylol Phenylcarbylamine chloride Phosphorus oxychioride (reacts) Salicylaldehyde Toluene diiuocyante (reacts) Vinyl bromide c-Il ------- Category 7: Gas No persistent visible trace of substance spilt on land or other surface outside the water. Acatylase Antmonta Carbon monoxide chlorine Dimethylainine Ethyla . Fluorine MethsflthiOl (if warm) Mmhylan ’ 1 ne Nitric oxide Nitrogen dioxid./tetroxide Nitrous oxide Phosga. Sulfur diozids Vinyl bromide Vinyl cbloride 0 - 12 ------- Category 8: Color Ainmothuin dichromate (red- orange) Arnmonitun ferricyanide Cobalt nitrate Potassium dichrornate Sodium for ricyanid. Sodium dichromate Yellow Anunoniuni chromate Amrnoaiuzn trate Arninonium sulfide Ferric sulfate Nitric acid (undiluted.) Nitroaniline Nitrochiorobens one Nitroc resol Nitroxylol Phenylcarbylanline chloride Potassium chrornate Sodium (errocyanide Sodium chroxnate Quinacnne hydrochloride Quiz ne Titanium tetrachloride Green Nickel anunonium sulfate Nickel nitrate Quinhydrone Copper nitrate Copper sulfate Sodium fluoride (color added) Vanadyl sulfate c-I 3 ------- Miscellaneous Bromine (dark reddish-brown) Cb.IoroplatiniC acid (red-brown) Naphthylaznine (reddish) Nitrogen dioxide/tetroxide (red-brown) Sulfur chloride (amber-red) Cobalt chloride (pink-red if hydrated or dissolved) Cobalt sulfate (pink-red if hydrated or dii solved) Olsic acid (Commercial product yellow-red) Sodium sulfide (yellow-red) Ferric chloride (yellow-brown) Tannic acid (yellow-brown) Phosphorus pentasulfide (yellowish) Chlorine (greenish- yellow gas; amber liquid) Amnioniurn ferrocy 1 d . (yellow- green-blue) Ferrous sulfate (yellow- green) Nickel sulfate (yellow-green) Ferric hydroxide (brown) Glyconic acid (brown) Molasses (dark brown-black) Nickel chloride (brown-green) Nitric oxide (turns brown In air) Copper chloride (blue-green) Phosphorus (yellow or violet-red) Potassium permanganate (purple) Naphthenic acid (conunercial product dark) c—14 ------- Category 9: Fumes Acetyl bromide Acrylic acid Benzoy l chloride Boranes Chlorosulfonic acid Formic acid Hydrazine Hydrofluoric acid Nitric acid (fuming grade) Phosgene (liquid) Phosphorus oxychioride Phosphorus trichioride Sulfur chloride Sulfuric acid (fuming grade) Titanium tetrachioride C - I -S ------- Category 10: Vigorou . reaction Acetyl bromide Antimony trichioride (white sediment) Bensoyl cidoride Boranes Calcium carbide Calcium wsphide Chiorosuitnic acid fluorine Sodium (violent) Sulfur chloride titanium tetrachioride (violent) C— 16 ------- Category li: Odor- unpleasant Irritant (slinging, choking sensation, rather than “smell”) Acetyl bromide Acrylic acid (acrid) Ammonia (not unpleasant when dilute) Axnrnonium carbonate (not unpleasant when dilute) Bensoyl chloride Bromine Chlorine (not unpleasant when dilute) Chlorosulfonic acid C rotonaldehyde (acrid) Cyanogen bromide Cyanogen chloride fluorine Formaldehyde (biting, characteristic) Formic acid Hydrochloric acid Hydrofluoric acid Methyl acrylate (acrid) Methylethyl pyridine Nitric acid Nitrogen toidde!tetroxide Parafurmaldehyde (biting, formaldehyde) Phosphorus oxychloride Phosphorus trichioride Propazid (suffocating) Quinone Quinoline (sharp, unpleasant) Sulfur chloride Sulfur thor ide (characteristic) Sulfurous acid (sulfur dioxide) Toiuate dilsocyanate Sulfurous (roft egg) Aminoni*mi sulfide pitaanharne pentasulfide Foul (other than sulfurous) Carbon disulfide (commercial grade.) Methanethiol Thioglycolic acid c-17 ------- M i -s c” 1 laneous AU 1 L cbloride (sweetish) Butyl inercaptan (skunk) Calcium carbide (impure acetylene) Calcium phosphide (decaying fish) Naphthylnnine Phenylcarbylainine chloride (onion) Pyricline (nauseating) C- 18 ------- Category 12: Odor- not unpleasant Almond (both sweet and bitter) Benzoic acid B ensonitrile Cb lorobenzene Furfural Hydrocyanic acid Mtrobenzene Potassium cyanide Salicylaldehyde A.rnmoniacal (ammonia and amines) Amino ethyl ethanol amine Ammonia Arnmoniuzn carbonate Butylainthe Diaminoethane Diethanolamine Diethylamine Diisopropano lamine Diisopropy- Iaxnine Dimethylamine Ethylamine Ethyleneitnine Methylamine Monoe 1 ’ olarnine Monoisopropanolarni ne Propylarnine Triethanotamine Triethylanñne Trimcthytarn’ne Bensene (aromatic hydrocarbon) Bensene Ethyl benrene Styrene Toluene Xylene C- I S ------- fls ? ! (fruity, flowery) Acetaldehycle Ac etophenon. n-Aznyl alcohol a- Sutyl acetate Butyl alcohol Methyl acetate Polyglycol ether 4 sol (ph.nolic) Cresol Phenol Trichiorophenol Misc.’! * *OU$ Acetic acid (vinegar) Acetit anhydride (vinegar) Ammonium acetate (vinegar) Ace nitrlle (ether) Dichlormnetbane (ether) Propylene glycol (ether) Acryksnftrlle (biting) Calcium bypochlorite (biting - chlorine) Chlorine (clean biting odor when dilute) Hypochiorous acid (chlorine) Propanoic acid (sharp) Propanoic anhydride (sharp) Ally! chloride (mustard) Mustard gas (mustard/onion) Chloroform (neetish) Cyclohenne (sweetish) Thcbloroethane (sweetish) Dichiorupropane (sweetish) Ep&cblorohydrin (swectlsIfl Ethylene glycol (swetesh) Lead tetraethyl (sweetish) Ethyl alcohol (alcoholic, but often denatured) Methyl alcohol (alcoholic, but often denatured) Propyl alcohol (alcoholic) c - f l ------- Misceflaneous (continued) Dichlorobenzene (xnotbball) Naphthalene (mothball) Methylisobutyl ketone (carnphor} Octyl alcohol (penetrating, pleasant) Pentane (pleasant) Acetan dde (mousy) Aniline (characteristic) Carbon tetrachloride (cleaning fluid) Phoagene (CAUTION: toxic concentration NOT strongly irritant) Sodium sulfite (sulfurous) Naphthethc acid (commercial grades may be offensive) C- 21 ------- Category 13: Lacrimatory NOTE that many other substances induce eye watering in high concentration. Acetyl bromide Aflyl alcohol Allyl chloride Ammonia Bensoyl chloride Crotonaldehyde flhyl acrylate C-22 ------- Category 14: Flammable Highly flammable Acetaldehyde Acetic anhydride Acetonitrile Acetylene Ac rylo nitrite Allyl chloride Benz one Butyl mercaptan Carbon die ulfide Carbon monoxide Chiorobutadiene Crotonaldehyde Cyclohexane Diethylandne Dimethylandne Ethyl acrylate Ethyl alcohol Ethylunine Ethylene Ethyleneirnine Isoprene Methaneth iol Methanol Methylarnine Methyl methacrylate Pentane Pentene Petroleum products, light Phosphorus (yeflow) Propanat triethylainine Vinyl acetate Vinyl bromide Vinyl chloride C- 23 ------- Less flanrntahle n-Amyl acetate Bensonitrile Benzylaniine n- Butyl acetate Duty! alcohol Butyla inine Chiorobensene Eliaminoethane Dichioroethane Dichloropropafle Dii.opropyla ltüne Dirnethyl suibride Ethyl bensene Ethylene glycol Ethylene glycol diacetate Heptanol fls anpl Methyl acetate Methyl acrylate Methylethyl pyridine Methylisobutyl ketone Mono et hanolamine Monoisopr op*ThOlaIfl ine Nitrobensene Nitropropane Octyl alcohol Orydiproprionitrile Pentanal Pentanol Petroleum, crude; and heavy and medium products Propanoic acid Propanoic anhydñde Propyl alcohol Propylarnine Propylene glycol Propylene oxide Styrene Tetraethylene pentaniine Toluene Triethanola lnine )Cylene C- 24 ------- Category 15: Add Dilute solution (or hydrolysis products) acid to litmus. Acetic acid Acetic anhydride Acetyl bromide Aluminum sulfate Ainnoniurn acetate Beazoyl chloride Chiorosulfonic acid Chiorous acid fluorine Formic acid Hydrochloric acid Hydrofluoric acid Lactic acid Nitrous acid Oxalic acid Phosphoric acid Phosphorus orychioride Phosphorus pentasulfide Phosphorus trichloride Sodium bit ulfite Salicylic acid Sulfur chloride Sulfur diotde Sulfuric add Sulfurous acid Thioglycolic acid Zinc chloride Zinc nitrate Zinc sulfate Zirconium sulfate c-as ------- Category 16: Alkaline ThiMe solution (or products of reaction) alkaline to litmus. Alkyl aryl anunaniuni halides Ammonia Barium bydroride Bensylamine Dia Tni no etha n e fliethan niarnine Di.thy lam ine Dimethy lamine flhy lam in. Ethy len. indne H ne Pota.ssium hydrozide Propylan ’ 4 ne Sodium sulfide Sodium steante Sodium silicate Sodium oleate Sodium methylate Sodium hydroxide Sodium hydrosulfide Sodium cyanide Sodium —I p — a Tr ietha nn larn ine TriSby la ndne Trimethy la dne C- f l ------- Aikyl aryl ammonium halides Anionic surfactants Linoleic acid Neutral a urfactants Quaternary ararnothiun salts Sodium oleate Sodium pabnitate Sodium stearate e-27 * U, S. GOVERNMENT PRINTiNG OFFICE: 1974 0 - 532 -559 ------- |