ETV Source Water Protection

Residential Nutrient Reduction

Test Plan
for

The Massachusetts Septic System Test Center

for Verification Testing
of

Waterloo Biofilter® Nutrient Reduction Technology

Prepared for
National Sanitation Foundation International
and

Environmental Technology Verification Program
of the

US Environmental Protection Agency

Prepared by
Newton Millham, Westport Water Resources
672 Drift Road
Westport, MA 02790

Final Draft, February 12, 2001

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Executive Summary

This Test Plan is designed to verify nutrient reduction of the Waterloo Biofilter® treatment technology under the
US EPA Environmental Technologies Initiative Source Water Protection Program. The verification testing will be
conducted by the Barnstable County Department of Health at the Massachusetts Septic System Test Center.
During the testing, the Waterloo Biofilter® Model 4 Bedroom technology will be loaded with influent wastewater
from a sanitary sewer at the design hydraulic rate of 440 gpd.

The period of testing will consist of an eight-week startup period, and a twelve-month testing period incorporating
five stress periods with varying stress conditions, simulating real household conditions.

Monitoring of nutrient reduction will be by measurements of constituents which demand oxygen for treatment
(BOD and CBOD), and nitrogen species (TKN, NH4, NO2, NO3). Operational characteristics such as electric
use, laborto perform maintenance, maintenance tasks, durability of the hardware, noise and odor production will
be monitored.

The Plan includes a QAPP outlining the QA/QC measures incorporated into the Test Plan experimental design.

Deliverables from the monitoring will be in the form of sampling event reports, water quality data summary
reports, an operation and maintenance report and a QC and analytical report.

Technology Description

Physical Layout

The Waterloo BiofiIter® Model 4 Bedroom is a trickling filter that uses patented, open-cell foam as the filter
media. The Waterloo Biofilter® treatment technology consists of a septic tank, a small pump chamber and the
Biofilter® unit. Influent raw wastewater enters the 1,500 gallon septic tank, where it undergoes primary settling
and digestion. A Zabel A-300 effluent filter is placed in the outlet of the septic tank. Effluent from the septic tank
flows by gravity to a 20" diameter pump chamber. A 1/3 hp 110 VAC pump pumps on demand to the Biofilter® in
doses of approximately 6 gallons volume. The Biofilter® unit is an insulated wooden box 4 feet wide, 8 feet long
and 5 feet high with an internal volume of approximately 137 cu ft. The box is constructed of cedar and pressure
treated woods. The internal surfaces are sprayed with insulation and are watertight. Two baskets of dimensions
44" diameter and 54" high are filled with the patented Biofilter® foam cube media. Septic tank effluent from the
pump chamber is sprayed downward over the center of each basket through single spray nozzles which provide
distribution of the liquid over the top surface of each basket. A small diversion partition bisects the floor of the
Biofilter® unit beneath the two treatment baskets to direct the treated effluent from one half of each basket to
recirculate by gravity to the inlet end of the septic tank. Effluent from the other half of the floor flows by gravity as
forward flow to the drainfield. In this manner, 50% of the treated effluent is recycled through the septic tank. A
small control panel contains the pump actuator and an alarm.

Treatment theory

The Waterloo Biofilter® is a trickling filter that cleans household wastewater using a succesion of treatment steps.
Raw wastewater enters the septic tank where it undergoes primary settling of solids and fermentation under
anaerobic conditions. Organic nitrogen is ammonified in the septic tank. Primary treated effluent is then sprayed
over the Biofilter® media where naturally-occuring aerobic microbes degrade and oxidize organic pollutants, and
reduce coliform bacteria and other contaminants. The Biofilter® media provides a matrix with a large surface area
for the attached growth of a microbial population. Wastewater flows over and into the filter media on its passage
by gravity to the base of the Biofilter®. The media has inter-connected, internal void spaces that promote both
fluid and air movement. As organic contaminants are removed, ammonium is microbially oxidized to nitrate
(nitrification). Half of the treated and nitrified effluent is then recirculated to the inlet end of the septic tank. In this
anaerobic environment, dissolved nitrate is microbially converted to di-nitrogen gas that is released to the

atmosphere.

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ACRONYMS



BCDHE

Barnstable County Department of Health and the Environment

bod5

biochemical oxygen demand (five day)

CBOD5

carbonaceous biochemical oxygen demand (five day)

COC

chain-of-custody

EPA

United States Environmental Protection Agency

ETV

Environmental Technology Verification Program

GAI

Groundwater Analytical Inc.

MA SSTC

Massachusetts Septic System Test Center

mg/L

milligrams per liter

NELAC

National Environmental Laboratory Accreditation Council

NIST

National Institute of Standards and Technology

NSF

NSF International

PQL

practical quantitation limit

QA

quality assurance

QAPP

quality assurance project plan

QC

quality control

RPD

relative percent difference

SOP

standard operating procedure

TKN

total Kjeldahl nitrogen

WBS

Waterloo Biofilter® Systems Inc.

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Table of Contents

Chapter 1 Introduction	5

1.1	Background, objectives, test site description	5

1.2	Critical measurements, data quality indicator goals	6
Chapter 2 Project Organization 7

Chapter 3 Experimental Design	8

3.1	Test conditions	8

3.2	Sampling and monitoring points	9

3.3	Sampling frequency and type of samples	10

3.4	Sampling strategy and procedures	11

3.5	Evaluation of verification objectives	13

3.6	Health and safety plans	14

Chapter 4 Field Operation Procedures	14

4.1	Method to establish steady state	14

4.2	Site specific factors affecting monitoring	14

4.3	Site preparation	14

4.4	Monitoring procedures	14

4.5	Collection of representative samples	14

4.6	Split samples	14

4.7	Sample containers, volumes, holding times	14

4.8	Sample labeling, transport and archiving	14

Chapter 5 Analytical Procedures	16

5.1	Water quality methods	16

5.2	Method appropriateness	16

5.3	Calibrated measurements	16

5.4	Other measurements	16

Chapter 6 Quality Assurance Project Plan	18

6.1	QA/QC objectives	18

6.2	OA Indicators	18

6.3	Sampling equipment calibration	21

6.4	Water quality and operational control checks	21

6.5	Chain of custody	21

6.6	Acceptance criteria	22

6.7	Assessment of additional OA objectives	22

6.8	Corrective actions	22

6.9	Cross contamination	23

6.10	OA Structure	23

Chapter 7 Reports and other deliverables	25

7.1	Deliverables	25

7.2	Data reduction	26

Chapter 8 Assessments	27

8.1	Audits At MASSTC	27

8.2	Audits at BCDHE	27

8.3	Waste Management Plan	27

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1.0	Introduction

This Test Plan sets forth the experimental design, methods, measurements, Quality Assurance/Quality
Control meas ures and reports which will be used by the Barnstable County Department of Health and
the Environment to test and verify the nutrient removal performance of the Waterloo Biofilter® Model 4
Bedroom wastewater treatment technology.

1.1	Background

1.1.1	Nutrient Reduction

Verification of residential wastewater treatment technologies under the ETV Source Water Protection
Pilot's Protocol for Residential Nutrient Reduction Technologies is designed to verify the nutrient
removal performance of residential wastewater treatment technologies. In addition, the removal of the
oxygen-demanding contaminant load present in domestic wastewater by these technologies will be
verified.

The reduction of nutrients in wastewater discharged within watersheds is desirable from two
standpoints: first, reduction of watershed nitrogen inputs helps meet drinking-water quality standards for
nitrate and nitrite; and second, the reduction of both nitrogen and phosphorus helps protect the water
quality of receiving surface and ground waters from eutrophication and the consequent loss in
ecological, commercial, recreational and aesthetic uses of these waters.

Technologies which remove nutrients in on-site domestic wastewater include the following types of
biologically mediated technologies: aerobic trickling filters, aerobic submerged media filters, sand filters,
peat filters, and soil absorption-based technologies. Removal of nutrients can also be accomplished
chemically through the use of ion-exchange filters and chemical precipitation systems.

1.1.2	Verification Testing

The verification testing consists of the installation of a single residential wastewater treatment
technology at the MA Septic System Test Center. The testing facility has a source of suitable domestic
wastewater. The technologies will be dosed daily with wastewater at a rate of 100% of their rated
capacity using a daily flow-pattern which mimics the generation of wastewater in a residence. An eight-
week startup period will be followed by a twelve-month testing period.

Sampling frequency is monthly with additional five stress periods incorporating higher frequency
sampling.

1.1.3	Testing Objectives

The testing objectives include the verification of the nutrient removals, removals of other oxygen-using
contaminants and operational characteristics. Reduction in influent wastewater contaminants will be
determined by laboratory analysis. Nutrient analytes include ammonia-N, nitrate-N, nitrite-N, and total
Kjeldahl N. Other parameters to be measured include both CBOD and BOD, suspended solids, pH,
temperature, alkalinity, and dissolved oxygen.

Testing will include the collection of operation and maintenance characteristics ofthe technology
including the performance and reliability of technology components and the level of required operator
maintenance. The test will identify and assess environmental inputs and outputs including chemical
usage, energy usage, generation of byproducts or residuals, noise and odors.

1.1.4	Test Site Description

The Massachusetts Septic System Test Center is located at Otis Air National Guard Base, Bourne, MA.
Domestic wastewater is supplied from a sanitary sewer serving Base residential housing and other
military usage buildings. Average influent wastewater characteristics are as follows: BODs =181 mg/L,
std. dev. = 61, n = 93; TSS =159 mg/L, std. dev. = 59, n = 81; Total Nitrogen = 34.4 mg/L, std. dev. =
4.6, n = 61; alkalinity = 168 mg/L, std. dev. = 27.5, n = 58; pH = 7.37, std. dev.. =0.13, n = 88. Influent
wastewater is pumped to a central dosing channel at the rate of approximately 26,000 gallons per 18
hour daily cycle. Raw wastewater circulates through the dosing channel and excess wastewater,
approximately 20,000 gallons, is returned by gravity to the sanitary sewer for treatment at the Base
wastewater treatment plant. Within the dosing channel there are four circulation pumps which keep
wastewater constantly flowing within the channel to ensure the suspension of solids and equal quality of
wastewater at all points within the channel. Dosing is accomplished by individual pumps, one per

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technology, set in the dosing channel. Volumetric doses are controlled by a programmable logic
controller, and occur in 15 equal dosing events of between 22 and 33 gallons per dose depending upon
technology rated capacity.

1.1.5 Equipment Capabilities and Description
Physical Layout

The Waterloo BiofiIter® Model 4 Bedroom is a trickling filter that uses patented, open-cell foam as the
filter media. The Waterloo Biofilter® treatment technology consists of a septic tank, a small pump
chamber and the Biofilter® unit. Influent raw wastewater enters the 1,500 gallon septic tank, where it
undergoes primary settling and digestion. A Zabel A-300 effluent filter is placed in the outlet of the
septic tank. Effluent from the septic tank flows by gravity to a 20" diameter pump chamber. A 1/3 hp 110
VAC pump pumps on demand to the Biofilter® in doses of approximately 6 gallons volume. The
Biofilter® unit is an insulated wooden box 4 feet wide, 8 feet long and 5 feet high with an internal volume
of approximately 137 cu ft. The box is constructed of cedar and pressure treated woods. The internal
surfaces are sprayed with insulation and are watertight. Two baskets of dimensions 44" diameter and
54" high are filled with the patented Biofilter® foam cube media. Septic tank effluent from the pump
chamber is sprayed downward over the center of each basket through single spray nozzles which
provide distribution of the liquid over the top surface of each basket. A small diversion partition bisects
the floor of the Biofilter® unit longitudinally so that 50% of the effluent from each basket goes to the
outlet to the septic tank, and 50% goes to disposal. A small control panel contains the pump actuator
and an alarm.

Treatment theory

The Waterloo Biofilter® is a trickling filter that treats household wastewater using a succesion of
treatment steps. Raw wastewater enters the septic tank where it undergoes primary settling of solids
and fermentation under anaerobic conditions. Organic nitrogen is ammonified in the septic tank. Primary
treated effluent is then sprayed over the Biofilter® media where naturally-occuring aerobic microbes
degrade and oxidize organic pollutants, and reduce coliform bacteria and other contaminants. The
Biofilter® media provides a matrix with a large surface area for the attached growth of a microbial
population. Wastewater flows over and into the filter media on its passage by gravity to the base of the
Biofilter®. The media has inter-connected, internal void spaces that promote both fluid and air
movement. As organic contaminants are removed, ammonium is microbially oxidized to nitrate
(nitrification). Half of the treated and nitrified effluent is then recirculated to the inlet end of the septic
tank. In this anaerobic environment, dissolved nitrate is microbially converted to di-nitrogen gas that is
released to the atmosphere.

Equipment capability

For normal household wastewater strength, the expected effluent quality is: BOD, 0-15 mg/L; TSS, 0-10
mg/L; and total nitrogen, 20-60% removal.

1.2 Critical Measurements

1.2.1	Critical measurement

For this test plan we define a critical measurement as a measurement whose absence would
significantly lower the confidence in the data and would affect the ability to verify system performance.
In the event data is lost or is deemed otherwise unacceptable, critical measurements must be repeated
within a time period which would allow substitution so as not impair the final data set.

Critical measurements of the verification plan fall into two categories: 1) measurement and
characterization of the nutrient and other contaminant removal performance of the
technologies; and 2) measurements and observations of technology operational
characteristics.

1.2.2	Data Quality objectives

Data quality objectives for the first category in 1.2.1 above include the acquisition of sufficient correct
analytical measurements of contaminant removal performance, in order to credibly characterize the
long-term removal performance of the technology under varying climatic conditions.

The principal users of this data will be the technology vendor, Waterloo Biofilter® Systems Inc. to gain
regulatory approvals for use in marketing. Secondary users of this data will be the various state,
regional and local approving and planning authorities in the United States. Likely secondary data users
also will include system installation engineers and designers and consumers.

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Data quality objectives for the second category 1.2.1 are the development of sufficient correct
operational and environmental data about the technology to characterize the reliability, cost and
environmental operational characteristics (i.e., noise and odor) of the technology. The principal users of
this data are consumers and designers. Secondary users for the information are state, regional and
local approving and planning authorities in the United States

1.2.3	Data quality indicator goals

Data quality indicator goals are to be met through the use of certified laboratories using EPA or
Standard Methods with appropriate QA/QC for all off-site analyses. Field measurement data quality
indicator goals are to be met through the use of Standard Methods and application of a QA/QC plan for
the field testing.

1.2.4	Testing plan schedule

The testing plan schedule includes three phases: 1) a pre-installation communication between the
verification organization, testing organization and the participating vendor, (Waterloo Biofilter® Systems
Inc.) and installation of the technology, which may require up to three months; 2) the start-up period of
up to eight weeks wherein Waterloo Biofilter® Systems Inc. is provided with time for the technology to
come to a steady-state operational condition; Waterloo Biofilter® Systems Inc. has the option of
indicating when the technology is ready to begin testing. 3) the twelve-month operational testing
period. A detailed weekly schedule of the testing period is provided in Table 3-2.

1.2.5	Milestones

Milestones for the testing include: 1) the completion of technology installation and start-up; 2) the
completion of the startup period (up to eight weeks); 3) the completion of the twelve month testing
period; and 4) the reporting of data.

2.0 Project Organization

U.S. Environmental Protection Agency (EPA):

Project Officer. ETV Source Water Protection Pilot Ray Frederick, Urban Watershed Branch,

Water Supply & Water Resources Division, NRMRL U.S. EPA, 2890 Woodbridge Ave.,
Edison, NJ 08837-3679 732-321-6627 frederick.ray@epa.gov

NSF International (NSFV P.O. Box 130140, Ann Arbor, Ml 48113-0140 734-769-8010

Project Manager, ETV Source Water Protection Pilot: Tom Stevens 734-769-5347
stevenst@nsf.org

Project Coordinators. ETV Source Water Protection Pilot: Maren Roush 734-827-6821
mroush@nsf.org: Michelle Forcier. 734769-5277. forcier@nsf.org.

Testing Organization (TO): Barnstable County Department of Health and the Environment
(BCDHE); Superior Court House (P.O. Box 427), Barnstable MA 02630 508-375-6000

Project Manager: George Heufelder, Barnstable County Department of Health and the Environment
(BCDHE), 508-375-6616, gheufeld@capecod.net

BCDHE Laboratory Manager: Thomas Bourne, Barnstable County Department of Health and the
Environment (BCDHE) 508-375-6606 @capecod.net

Sub-contract Laboratory: Groundwater Analytical. Inc. (GWI)228 Main St. Buzzards Bay, MA
02532

GAI Laboratory Manager: Eric Jensen; 508-759-4441

Facility Operations Manager: Sean Foss, Barnstable County Department of Health and the
Environment (BCDHE), 508-563-6757, sfoss@capecod.net.

Project QA Officer: Thomas Bourne 508-375-6606

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3.0	Experimental Design

3.1	Test Conditions

The Waterloo Biofilter® unit shall be assembled, installed and filled in accordance with the Waterloo
BiofiIter® Systems Inc.'s specifications at the Massachusetts Septic System Test Center (MASSTC).
Waterloo Biofilter® Systems Inc. shall inspect the system for proper installation, and if no defects are
detected and the system is determined to be structurally sound it shall be placed into operation in
accordance with Waterloo Biofilter® Systems Inc.'s 'start up procedures". If Waterloo Biofilter® Systems
Inc. does not provide a filling procedure, 2/3 of the system's capacity shall be filled with water and the
remaining 1/3 shall be with residential wastewater.

When possible, electrical or mechanical defects shall be repaired to prevent evaluation delays. All
repairs shall be recorded in the test log.

3.1.1	System Operation

The system shall be operated in accordance with Waterloo Biofilter® Systems Inc.'s instructions.

Routine service and maintenance of the system shall not be permitted during the performance and
evaluation period unless specified in the O&M manual by Waterloo Biofilter® Systems Inc.

3.1.2	Phases ofTestina

The system shall undergo design loading of wastewater for a minimum of one (1) year following a
maximum start-up period of eight (8) weeks. When the technology performance has stabilized during
the start-up period, Waterloo Biofilter® Systems Inc. shall advise the Testing Organization that the
evaluation period can commence. This notice shall be in writing to the Verification Organization. The
one-year evaluation period duration will allow for an assessment of the impact of seasonal variations on
performance.

3.1.3	Influent Flow Pattern

The influent flow dosed to individual technologies will be through the use of timed pump operation and
will conform to the following pattern as representative of a typical residence(s) scenario:

6 a.m. - 9 a.m.	approximately 33% of total daily flow in 5 doses

11 a.m. - 2 p.m.	approximately 27% of total daily flow in 4 doses

5 p.m. - 8 p.m.	approximately 40% of total daily flow in 6 doses

Total daily flow shall be within 100% ± 10% of the rated capacity of the technology (Waterloo Biofilter®:
440 gallons per day) undergoing testing based on a thirty (30) day average with the exception of
periods of stress testing described in Section 3.1.4. Influent dosing pumps are controlled by a
programmable logic controller which permits timing of the fifteen individual doses to the second.

3.1.4	Stress Testing

One stress test shall be performed following every two months of normal operation during the
technology evaluation, so that each of the five stress scenarios is addressed within the twelve (12)
month evaluation period.

Stress testing shall involve the following simulations:

Wash-day stress
Working parent stress
Low-loading stress
Power/equipment failure stress
Vacation stress

Wash-dav stress simulation shall consist of three (3) wash-days in a five (5) day period with each wash-
day separated by a 24-hour period. During a wash-day, the technology shall receive the normal flow
pattern (Section 3.1.3); however, during the course of the first two (2) dosing periods per day, the
hydraulic loading shall include three (3) wash loads [three (3) wash cycles and six (6) rinse cycles]. The
volume of washload flowto the technology will be standardized for all washloads (28 gallons). Common

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(readily available to consumers) detergent and non-chlorine bleach shall be added to each wash load at
Waterloo BiofiIter® Systems Inc.'s recommended loading.

Working parent stress simulation shall consist of five (5) consecutive days when the technology is
subjected to a flow pattern where approximately 40% of the total daily flow is received between 6 a.m. -
9 a.m. and approximately 60% of the total daily flow is received between 5 p.m. and 8 p.m., which shall
include one (1) wash load [one (1) wash cycle and two (2) rinse cycles],

Low-loadina stress simulation shall consist of testing the technology for 50% of the design flow loading
for a period of 21 days. Approximately 35% of the total daily flow is received between 6 a.m. - 11 a.m.,
approximately 25% of the flow is received between 11 a.m. - 4 p.m., and approximately 40 % of the
flow is received between 5 p.m. and 10 p.m.

Power/eguipment failure stress simulation shall consist of a standard daily flow pattern until 8 p.m. on
the day when the power/equipment failure stress is initiated. Power to the technology shall then be
turned off at 9 p.m. and the flow pattern shall be discontinued for 48 hours. After the 48-hour period,
power shall be restored and the technology shall receive approximately 60% of the total daily flow over
a three (3) hour period which shall include one (1) wash load [one (1) wash cycle and two (2) rinse
cycles].

Vacation stress simulation shall consist of a flow pattern where approximately 35% of the total daily flow
is received between 6 a.m. and 9 a.m. and approximately 25% of the total daily flow is received
between 11 a.m. and 2 p.m. on the day that the vacation stress is initiated. The flow pattern shall be
discontinued for eight (8) consecutive days with power continuing to be supplied to the technology.
Between 5 p.m. and 8 p.m. of the ninth day, the technology shall receive 60% of the total daily flow,
which shall include three (3) wash loads [three (3) wash cycles and six (6) rinse cycles],

3.2 Sampling and monitoring points

3.2.1	Influent wastewater

Raw influent wastewater will be sampled from the dosing channel at a point near the technology dosing
pump intake, at a point between four and six inches from the channel floor.

3.2.2	Intermediate Effluent (Not applicable for Waterloo Biofi Iter®)

3.2.3	Final effluent

Technology effluent shall be sampled from the 4 inch effluent line of the Waterloo Biofilter® treatment
unit at a point nearest the effluent discharge of the technology.

A grab sample will be withdrawn from the influent sampling point for the measurement of pH and
temperature. A grab sample for pH and temperature at the intermediate and treated effluent locations
will be withdrawn from the sampling points during periods when flow is occurring at the sampling point.
Dissolved oxygen will be measured at the treated effluent locations when flow across the sampling point
is occurring, (referto Table 3-1).

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TABLE 3-1
SAMPLING MATRIX





SAMPLE
LOCATION

SAMPLE
LOCATION



PARAMETER

SAMPLE TYPE

INFLUENT

FINAL EFFLUENT

TESTING
LOCATION

BODs

24 Hour composite

V



Laboratory

CBODs

24 Hour composite



V

Laboratory

Suspended Solids

24 Hour composite

V

V

Laboratory

PH

Grab

V

V

Test Site

Temperature (°C)

Grab

V

V

Test Site

Alkalinity (as CaCCfe)

24 Hour composite

V

V

Laboratory

Dissolved Oxygen

Grab



V

Test Site

TKN (as N)

24 Hour composite

V

V

Laboratory

Ammonia (as N)

24 Hour composite

V

V

Laboratory

Total Nitrate(as N)

24 Hour composite



V

Laboratory

Total Nitrite (as N)

24 Hour composite



V

Laboratory

3.3 Sampling frequency and types

3.3.1	Sampling frequencies
Normal Monthly Frequency

Sampling frequency will be at a minimum of once per month. Additional samples will be taken in
conjunction with the stress tests and final week as outlined in the following sections.

Stress Test Frequency

Samples shall be collected on the day each stress simulation is initiated and when approximately 50%
of each stress test has been completed (Note: For the Vacation and Power/Equipment failure stresses,
there is no 50% sampling). Beginning twenty-four (24) hours afterthe completion of wash-day, working-
parent, low-loading, and vacation stress scenarios, samples shall be collected for six (6) consecutive
days. Beginning forty-eight (48) hours afterthe completion of the power/equipment failure stress,
samples shall be collected for five (5) consecutive days.

Final Week

Samples shall also be collected for five (5) consecutive days at the end of the yearlong evaluation
period.

Table 3-2 shows a hypothetical sampling schedule based on the NSF/ETV Nutrient Reduction Protocol
requirements.

3.3.2	Sample types
Composite Samples

Composite samples are to be drawn using automated samplers at each sample collection point cited in
Section 3.2.1 and Table 3.1. Automated samplers will be programmed to draw equal volumes of sample
from the waste treatment stream at the same frequency, number (15) and timing as influent wastewater

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doses to the relevant technology. Samples taken in this manner will therefore be flow proportional.
Initiation of individual automated sampler events will be offset or delayed to correspond to the passage
of a flow pulse through the relevant sample collection point.

Grab Samples

Grab samples for pH and temperature will be obtained from the influent wastewater stream at the
location of the automated sampler intake. Grab samples forthe measurement of pH, temperature and
dissolved oxygen are to be obtained at the same locations as the automated sampler intake for the final
technology effluent.

QC Samples

QC samples shall be taken at the rate of one field sample split per sampling event forthe monthly
samples. Samples will be split in the field by drawing all sub-samples from the composite container.
During stress test sampling field sample splits shall be taken at least once per stress event.

Raw sample retention

Sample remaining in the bulk composite sample containers shall be retained at 4 degrees Celsius for 24
hours following field sampling. In the event of transportation or laboratory sample loss, this retained
sample may provide additional sub-sample volume for analysis.

3.4 Sampling strategy and procedures

3.4.1	Sampling Site Selection Rationale
Influent Wastewater

The influent wastewater sampling site selection rationale is based upon the layout of the dosing channel
at the MASSTC facility. Raw wastewater enters the sixty-six foot long dosing channel via two pipes
midway between the channel end and the channel outlet. Dosing pumps for individual technologies are
located in-line along the dosing channel. The Influent wastewater sampling site will be located close to
the Waterloo Biofilter® dosing pump to ensure a representative sample of wastewater is obtained.

Intermediate Technology Effluent (Not Required by Waterloo Biofilter®)

Waterloo Biofilter® Effluent

For the Waterloo Biofilter® effluent, the sampling site will be located in the distribution box, where the
effluent pipe leading from Waterloo Biofilter® discharges. During installation and setup of the Waterloo
Biofilter®, a sampling point consisting of a tee-cross with sump of sufficient size to retain sample volume
for both grab and automated sampler will be installed on the end of this pipe. Note that the sump is only
large enough to retain approximately one liter of fluid and be readily flushed and replenished by the
normal flow of treated effluent. The sump shall also be accesible so that it may be cleaned of attached
and settled solids on a regular basis priorto sampling dates.

3.4.2	Sample Type Selection Rationale

Selection of the types of samples, grab or composite is dictated by the ETV SWPP Nutrient Reduction
Protocol for which this plan is intended. The selection of composite samples for the majority of
parameters reflects the tendency of a composite sample to provide a more representative sample in the
face of the established daily variability of influent wastewater strength and character and is a
compromise with sample holding time restrictions. In contrast, grab samples for pH, temperature and
dissolved oxygen are parameters best measured from fresh sample obtainable as a grab.

For details concerning the acquisition of composite and grab samples please refer to the MA
Test Center SOPS (Attachment I; Section 1)

3.4.3	Sample Frequency Selection Rationale

Selection of the frequencies of sampling has been established by the ETV SWPP Nutrient Reduction
Protocol. Samples shall be collected at a minimum interval of once per month at all sampling locations
(See Table 3-2).

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Table 3-2
Sampling Schedule

StartuD Period (ud to f

3 weeks): Samples shall be collected once during week 3, 5, 6, and 7.





Testina Period:
Week 1-8:

Samples shall be collected once per month





Week 9:
Week 10:

Wash Day stress initiated on day 1 of Week 9. Samples shall be collected

on day 1, day 3, day 6 and day 7 of Week 9.

Samples shall be collected on day 1 through 4 ofweek 10.

Week 11-17

Samples shall be collected once per month





Week 18
Week 19

Working Parent stress initiated on Day 1 of week 18. Samples
collected on Day 1, Day 3 and Day 6 and 7 ofWeek 18.

Samples will be collected on Day 1 through day 4 ofWeek 19.

will

be

Week 20-27

Samples shall be collected once per month.





Week 28

Week 29-30
Week 31

Low-loading Stress initiated on Day 1 of Week 28. Samples

collected on Day 1 ofWeek 28.

Samples will be collected on Day 4 ofWeek 29.

Samples will be collected on Day 1 though 6 ofWeek 31.

will

be

Week 32-38

Samples shall be collected once per month.





Week 39
Week 40

Power/equipment Failure stress initiated on Day 1 of Week 39. Samples
will be collected on Day 6 and Day 7 ofWeek 39.

Samples will be collected on Day 1 through 3 ofWeek 40.

Week 41-47

Samples shall be collected once per month.





Week 48

Week 49
Week 50

Vacation Stress initiated on Day 1 of Week 48. Samples will be taken on
Day 1 ofWeek 48.

Samples shall be collected on Day 4 through 7 of Week 49.

Samples shall be collected on Day 1 ofWeek 50.

Week 51
Week 52

No sample will be taken this week.

Samples shall be collected on Day 1 through Day 5 ofWeek 52.





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Table 3-3
Test Specific Target Parameter Table

Operational Venue

Measurement

Target Analytes

Critical

Non-Critical



Type

Analyte or Measure





Influent

Chemical Analysis

BOD5

X



Wastewater



pH



X





Alkalinity

X







TKN

X







Ammonia (as N)

X





Assay

Suspended Solids

X





Physical

Temperature



X





Volume

X





Chemical Analysis

CBOD5

X



Final Effluent



pH



X





Alkalinity

X







TKN

X







Ammonia (as N)

X







Orthophosphate (as P)

X







Dissolved Oxygen



X



Assay

Suspended Solids

X





Physical

Temperature



X

Byproducts/

Assay

TSS

X



Residues



VSS



X



Physical

Volumetric

X



Environmental

Assay

Noise



X





Odor



X

Operation &

Physical

Kilowatt usage

X



Maintenance



Chemical Usage

X



Monthly Alarms test



Alarm light and Buzzer



X

Electrical Components



Failure/Bearings/Deterioration of



X





control/junction boxes





Structural integrity



Operator Observation



X

3.5 Evaluation of Verification Objectives

3.5.1 Evaluation of Nitrogen Removal Data

Laboratory analytical data will be evaluated for acceptance based on the data falling within QA/QC
limits as reported by BCDHE and GAI laboratories and outlined in relevant laboratory SOP's
(Attachments II and III).

The data produced by the field analytical measures at the MA SSTC testing facility will be evaluated as
falling within acceptable QA/QC limits for those measures as outlined in the MA SSTC SOP (attachment
I). Measurements of influent flow and volumetric use of technology process chemicals will be evaluated
for acceptance on the basis of meeting the stated QA/QC objectives for those measures as outlined in
the MA SSSTC SOP.

Observations of the Waterloo Biofilter® operational characteristics, environmental characteristics and
measures, and alarm tests will be evaluated on the basis of these measures compliance with the
relevant QA/QC requirements for recording observations, electric use and alarm tests.

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3.6 Safety and hygiene plan

The MA SSTC safety plan is attached. The BCDHE laboratory has a health and safety plan on file and
available upon request.

4 Field Operation Procedures

4.1	Method to establish steady state

Waterloo Biofilter® Systems Inc. will advise BCDHE when the technology is ready for commencement of
evaluation. Alternately, the Waterloo Biofilter® Systems Inc. may indicate the parameter values that
indicate the system is ready. As noted in the protocols, this period does not extend beyond 8 weeks,
but may, at Waterloo Biofilter® Systems Inc.'s prerogative, be shorter.

4.2	Site Specific Factors affecting sampling monitoring procedures. Refer to MA SSTC SOP
(Attachment I Section 1) for sampling strategy.

4.3	Site preparation needed prior to sampling monitoring (Please refer to MA SSTC SOP (Attachment
I) for sampling strategy and sampler setup.

4.3.1 Tee-cross sampling points

Installation of PVC tee-cross sampling access sumps will be required during or after the installation of
the Waterloo Biofilter® technology. These tee crosses will be installed as outlined in section 3.4.1 and
above.

4.4	Monitoring procedures for the MA Test Center are incorporated within the MA Test Center SOP
(Attachment I Section 1). Set-up, programming and calibration of the automated samplers for composite
sampling is discussed in detail in that section. Splitting of composite samples at the MA SSTC is also
discussed in detail in Section 2 of Attachment I. Labeling of samples, chain of custody and sample
transport are discussed in Section 2 of Attachment I.

4.5	Collection of representative samples is ensured through the use of automated, composite
samplers to collect all major samples except pH, Temperature and dissolved oxygen that are more
appropriately measured with grab samples. Programming of the automated samplers is to be
synchronized with influent dosing events, and ensures that samples collected are flow-proportional.
Sample volumes delivered by the automated samplers are self-calibrated by the sampler and calibrated
by hand on a monthly basis and recorded in the Field Log as per MASSTC SOPS, Attachment I,

Section 1.3.

Shaking of composite containers prior to pouring sub-samples into containers for transport to BCDHE
and GAI laboratories ensures that sub-samples are representative of the original composite sample.
(Refer to MA SSTC SOP Attachment I; Section 2).

4.6	Split samples

Split sample frequency and methods are discussed in Sections 2.1-2.5 of MA SSTC SOP, Attachment I.

4.7	Sample containers, volumes and holding times

Sample containers, volumes and holding times are shown in Table 4- 1 and are discussed in detail in
Attachment I; Section 2. Sample preservation is discussed in Section 2.0, MA SSTC SOP, Attachment I.

4.8	Sample labeling, transport and archiving

Samples will be labeled with the standard BCDHE adhesive label. Information required to complete this
label includes the following items of information: (Dummy data in parenthesis)

Barnstable County Department of Health and the Environment, Barnstable, MA 508-362-2511
Ext 337

Sample Client: (NSF)

Sample Date: (1/1/01)

Time of Collection: (09:15)

Location: (MASSTC)

Sampling ID: (WBS Influent) (WBS Effluent)

Collected by: (T.M., G.H.)

Preservative: (Ice, H2S04)

Analysis Requested (BOD, CBOD, N02, NH4, TKN, TSS, P04, TP, alkalinity)

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Sample Transport

BCDHE personnel will transport samples to the BCDHE laboratory via automobile. The samples will be
in coolers packed with ice to maintain the temperature of all transported samples at 4° C. Sub-sample
containers to be analyzed at the GAI laboratory will be transported from BCDHE laboratory to GAI in
GAI vehicle by GAI personnel. Travel time to BCDHE is approximately 40 minutes. Travel time from
BCDHE to GAI is approximately 45 minutes.

Sample Archiving

The remaining sample of raw composite will be retained for 24 hours at 4°C at the MA SSTC facility.

Table 4-1
Sample Holding Time Requirements

Analyte

Sample
Location

Container

Holding Time



BODs

Influent

250 ml Nalgene

48 hr.

CBODs

Effluent

1 liter Nalgene

48 hr

Suspended Solids

Influent

250 ml Nalgene

7 days

Suspended Solids

Effluent

1 liter Nalgene

24 hr

PH

All

250 ml sample cup

1

Temperature

All

250 ml sample cup

1

Alkalinity

All

250 ml Nalgene

6 hr

Dissolved oxygen

Effluent

250 ml sample cup

1

TKN2

All

250 ml acidified bottle

24 hr

Ammonia2

All

250 ml acidified bottle

24 hr

Total Nitrate/Nitrite

Effluent

250 ml Nalgene

24 hr

1.	pH, Temperature and D.O. will be measured immediately following recovery of sample at MA SSTC field location.

2.	TKN and Ammonia use a common pre-acidified bottle for all locations.

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5 Analytical procedures

5.1 Water quality methods

Water quality parameters and analytical methods are listed in Table 5-1.

Table 5-1
Water Quality Analytical Methods

is Parameter

Facility

Acceptance
Criteria

Acceptance
Criteria

Standard Method





Duplicates (%)

Spikes (%)



BOD5

BCDHE Laboratory

80-120

N/A

Method #5210 B*

CBODs

BCDHE Laboratory

80-120

N/A

Method #5210B

Suspended Solids

BCDHE Laboratory

80-120

N/A

Method #2540 D

pH

On-site

90-110

N/A

Method #423

Temperature (°C)

On-site

90-110

N/A

Method #2550

Alkalinity

BCDHE Laboratory

80-120

N/A

Method #2320

Dissolved Oxygen

On-site

80-120

N/A

Method #4500

TKN (as N)

GAI Laboratory

80-120

80-120

EPA 351.4"

Ammonia (as N)

BCDHE Laboratory

80-120

80-120

EPA 350.1

Total Nitrite (as N)

BCDHE Laboratory

90-110

60-140

EPA 353.3

Total Nitrate (as N)

BCDHE Laboratory

90-110

60-140

EPA 353.3

*Standard Methods forthe Examination of Water and Wastewater, APHA, 19th ed., (1995).

"""Methods for Chemical Analysis of Water and Wastes, US EPA, EPA-600/4-790-20, Revised (1983)
and Methods forthe Determination of Inorganic Substances in Environmental Samples, US EPA,
EPA/600/R-93/100, (1993).

5.2	Methods listed in Table 5-1 are approved forthe analysis wastewater and effluent.

5.2.1 Reporting Units

Reporting units are listed in Table 6-1

5.3	Calibrated measurements

5.3.1	BCDHE Calibrations

Calibration procedures for analytes measured at the BCDHE facility in Table 5-1 are contained in the
Barnstable County Department of Health Laboratory Standard Operating Procedures available at
BCDHE.

5.3.2	GAI QA/QC

Summaries of QA/QC procedures for analytes to be measured by Groundwater Analytical, Inc. are
attached as Attachment 2. A detailed QA/QC procedure is available at GAI.

5.3.3	MASSTC QA/QC

Calibration procedures for pH and dissolved oxygen are included in the MA SSTC SOP Section 2.5,
Attachment I.

5.4	Other Measurements

5.4.1 Influent wastewater

Measurement of operational facility and technology parameters otherthan those listed in Tables 5-1,
include volume of influent wastewater dosed to the Waterloo BiofiIter® technology and will include
electric use, chemical use, and by-product volumes and characteristics.

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5.4.2	Electric Use

Electrical use as recorded by the dedicated electric meter serving the Waterloo Biofilter® will be
recorded biweekly in the Field Log by BCDHE personnel. The meter's manufacturer and model number
and any claimed accuracy forthe meter will be noted in the Field Log. Following the end of the testing
period the electric meter will be returned to the manufacturer for calibration and the calibration data will
be entered in the Field Log.

5.4.3	Chemical Use

For this ETV testing, the Waterloo Biofilter® does not add process chemicals to achieve treatment.

5.4.4	Environmental Considerations
Noise

Noise levels associated with mechanical equipment shall be verified during the evaluation period. A
decibel meter shall be used to measure the noise level associated with the technology. Measurements
shall be taken one meter from the source(s) at one and a half meters above the ground, at 90° intervals
in four (4) directions. Any mitigation measures for noise control provided by the Waterloo Biofilter®
Systems Inc. shall be noted. Noise levels shall be measured once during the evaluation, approximately
one month after completion of start-up period. The meter shall be calibrated prior to use, either at the
Test Facility or by the lessor. Meter readings shall be recorded in the Field Log. Repeated or duplicate
measurements at each quadrant shall be made to account for variations in ambient sound levels.
Duplicated measurements shall be expressed as the geometric mean of the measurements. Noise
measurements shall be made at times of the day when ambient noise levels are at there lowest, for
example on a weekend morning and when wind speed is at a minimum and during times when there
are no Air Base flight operations.

Odors

Monthly observations shall be made by the Testing Organization during the evaluation period with
respect to odors generated by the Waterloo Biofilter® technology. The observation shall be qualitative
and shall include odor strength (intensity) and type (attribute). Intensity shall be as non-detectable;
barely detectable; moderate; and strong. Observations shall be made during periods of low wind
velocity (<10 knots) and will be made standing upright at a distance of three (3) feet from the treatment
unit, at 90° intervals in four (4) directions. All observations shall be by the same BCDHE employee.

If the treatment system is buried, covered or otherwise has odor containment, the means of ventilating
the compartment(s), including any odor treatment systems shall be noted in the Field Log.

5.4.5	Mechanical Components

Performance and reliability of the mechanical components (pump) shall be observed and documented
during the test period. This will include the recording in the Field Log of equipment failure rates,
replacement rates, and the existence and use of duplicate or standby equipment.

Alarms

During the evaluation period, any alarm systems associated with the technology shall be operationally
tested and verified at least once per month. The Waterloo Biofilter® has two alarms to indicate high and
low water conditions, respectively, that are activated by floats in the pump chamber. These alarms shall
be operated by lifting floats to activate. Responses of the alarms (Does the alarm sound or not?) to
testing shall be recorded in the Field Log.

5.4.6	Electrical/Instrumentation Components

Electrical components, particularly those that might be adversely affected by the corrosive atmosphere
of a wastewater treatment process, and instrumentation and alarm systems shall be monitored for
performance and durability during the course of verification testing. Observations of physical
deterioration shall be noted in the Field Log. Electrical equipment failure rates, replacement rates, and
the existence and use of duplicate or standby equipment shall be noted and recorded in the Field Log.

5.4.7	Residuals and Byproducts

Byproducts or residuals, when generated, may include septage and sludge. The quantity and quality of
residuals generated during the evaluation process shall be recorded in the Field Log. Measurement of
sludge depth shall be made twice during the testing period once after six months and once in the final
month of testing. A coring sludge measurement tool (Core Pro) shall be used to estimate the depth of
sludge/solids in the 1,500 gallon septic tank. Measurement of the sludge depth shall be repeated at
three locations within the septic tank area accessible to each of the two access manholes. Samples of

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sludge shall be recovered from the Core Pro during the final measurement period (Month 14) by
emptying the probe contents into a clean, sterile container and sending the sample to the BCDHE
laboratory for water content, VSS and TSS analysis.

It is not anticipated that solids will collect in the base of the Biofilter® unit. However visual checks will be
made to see if solids do collect there. Sampling of any accumulated solids will be by using a pole with
an attached scoop. Measurement of the thickness and areal extent of the solids deposits will be
recorded in the Field Log.

In the event residuals/solids are removed as a matter of regular operation and maintenance of the WBS
technology, the volume, mass and other characteristics of the byproducts or residuals (such as TSS,
VSS, water content.) shall be recorded in the Field Log.

6.0	Quality Assurance Project Plan

6.1	QA/QC Objectives

The QA/QC objective of this plan are to ensure that strict methods and procedures are followed during
this verification so that the data obtained from the testing are valid for use for the NSF ETV Nutrient
Reduction Protocols. The other QA/QC objective is to ensure that the conditions under which data are
obtained will be properly recorded so as to be directly linked to the data, should a question arise as to
its validity.

6.2	Quality Control Indicators

6.2.1	Precision

Precision is defined as the degree of mutual agreement relative to individual measurements of a
particular sample. As such, Precision provides an estimate of random error. Precision is evaluated
using analysis of field or matrix spiked duplicates. Method precision is demonstrated through the
reproducibility of the analytical results. Relative percent difference (RPD) may be used to evaluate
Precision by the following formula:

RPD=[(Ci- C2) + ((Ci + C2)/2)] x 100%

Where:

C-F Concentration of the compound or element in the sample
C2= Concentration of the compound or element in the duplicate

Please refer to Table 6-1 for field and laboratory methods for determination of precision.

6.2.2	Accuracy

For water quality analyses, accuracy is defined as the difference between the measured or calculated
sample result and the true value forthe sample. The closerthe numerical value of the measurement
comes to the true value or actual concentration, the more accurate the measurement. Loss of accuracy
can be caused by errors in standards preparation, equipment calibrations, interferences, and systematic
or carryover contamination from one sample to the next.

Analytical accuracy may be expressed as the percent recovery of a compound or element that has been
added to a sample at known concentrations prior to analysis. The following equation is used to
calculate percent recovery:

Percent Recovery = ( A-A0 )/A x100%

Where:

A= Total amount detected in spiked sample
Ao= Amount detected in unspiked s ample
At= Spike amount added to sample.

Analytical Accuracy

Analytical accuracy is ensured by following individual analytical method SOPs. Execution of random
spiking procedures for specific target constituents is summarized in the GAI QA/QC Summary

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(Attachment II) and BCDHE method QA Plan and method SOPs (Attachment III). Please refer to Table
6-1 for analytical method accuracy.

Field Sample Accuracy

Accuracy will be ensured for analyses conducted at the MA SSTC facility by use of calibration
standards and calibration procedures outlined in the MA SSTC SOP Section 2.6 (Attachment I).

Field process systems accuracy

Accuracy of influent dosing volumes and any chemical feed volumes measured during the test is
ensured by regular calibration of dosing pump deliver, chemical feed pump delivery (MA SSTC SOP,
Section 2; Attachment I).

Table 6 -1

Methodology for Measurement of Precision and accuracy

Parameter



Accuracy

BODs

(Report to the nearest 1 mg/l)

One sample per sample event or
10% of sample batch.

Refer to BCDHE laboratory SOP

CBODs

(Report to the nearest 1 mg/l)

One sample per sample event or
10% of sample batch.

Refer to BCDHE laboratory SOP

Suspended Solids

(Report to the nearest 1 mg/l)

One sample per sample event or
10% of sample batch.

Refer to BCDHE laboratory SOP

Alkalinity

(Report to the nearest 1 mg/l)

One sample per sample event or
10% of sample batch.

Refer to BCDHE laboratory SOP

TKN

(Report to the nearest 0.1 mg/l)

One sample per sample event or
10% of sample batch.

Refer to GAI laboratory QA/QC
summary

Ammonia

(Report to the nearest 0.1 mg/l)

One sample per sample event or
10% of sample batch.

Refer to BCDHE laboratory SOP

Total Nitrate/Nitrite

(Report to the nearest 0.1 mg/l)

One sample per sample event or
10% of sample batch.

Refer to BCDHE laboratory SOP

pH

(report to nearest 0.1 pH unit)

One sample per sample event or
10% of sample batch.

Daily 3-point calibration with certified
pH buffers in range of measurements
(4.0-10.0)

Temperature

O

(report to nearest 0.1 C)

One sample per sample event or
10% of sample batch.

Quarterly verification against BCDHE
Laboratory's NIST thermometer.

Dissolved Oxygen

(report to nearest 0.5 mg/l)

One sample per sample event or
10% of sample batch.

Daily calibration to internal standard
and reference to table of saturation
values.

For equipment operating parameters, accuracy refers to the difference between the reported operating
condition and the actual operating condition. For operating data, accuracy entails collecting a sufficient
quantity of data during operation to be able to detect a change in system operations.

Influent dosing flow rate

Assurance of the accuracy of influent flow rate to the technology is documented by MA SSTC SOP
(Attachment I, Section 8).

Electrical usage

Accuracy of electrical usage measurement will be assured by regular biweekly recording of meter
readings. Accuracy of the meter itself as claimed by the meter manufacturer, shall be noted along with

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model number and serial number of meter. Following the end of the testing period the electric meter will
be returned to the manufacturer for calibration and the calibration data will be entered in the Filed Log.

Chemical Usage

Chemical use is not applicable to the Waterloo Biofilter®, as no process chemicals will be added to the
treatment process.

6.2.3	Environmental Considerations
Noise

The sound meter for measurement of noise levels will be calibrated prior to use by the rental firm or
meter manufacturer and calibration information noted in the Field Log. Accuracy will be ensured by
conforming to ANSI/NSFI Std 40 protocols for noise measurement (Refer to Section 5.4.3 above).

Odor

Use of the term accuracy is not appropriate for a qualitative measurement instrument (the human nose).
However, the consistency of measurement of the monthly observations of odors will be ensured by use
of consistent location of measurement instrument (the human nose), consistency on odor description or
type, odor intensity and the measurement timing (Refer to Section 5.4.3 above for method of
observations).

6.2.4	Representativeness

Representativeness is the degree to which data accurately and precisely represent a characteristic of a
population, parameter variations at a sampling point, a process condition, or an environmental condition

Analytical procedures

Representativeness of laboratory procedures will be ensured by proper handling, storage and analysis
of samples so that the material reflects the material collected as accurately as possible.

Field samples

The representativeness of field samples is generally assessed by the collection of field duplicates
covering the range of concentrations for the particular parameter of interest encountered in this
verification Test Plan. Field sample representativeness is ensured by the use of composite sample for
influent and effluent samples.

6.2.5	Completeness
Start-up period completeness

Analytical results completeness

(No startup period data are required by the Test Protocols for technology removal performance.)
Influent volumetric measurements

Influent flow data completeness shall be determined as 85% of the total number of dosing days
being valid and acceptable.

Electric Use

Electric use completeness shall be determined as 83% of the biweekly meter readings.

Twelve-Month Sampling Period
Sampling

Completeness of sampling for monthly samples shall be determined as 83% of valid sampling
data from the monthly tests.

Completeness of sampling for stress tests will be determined as 83% valid sampling data from
each ofthe stress tests.

Analytical results completeness

Analytical results completeness will be determined as 90% of samples delivered to the BCDHE and
GAI laboratories shall be valid and acceptable.

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6.2.5 Comparability

Comparability of data for both GAI and BCDHE laboratories is ensured by the regular laboratory
certification program of the MA Department of Environmental Protection. Comparability will also be
addressed by sending duplicate samples to an independent Certified Laboratory (QA laboratory).

6.3 Sampling equipment calibration and frequency

6.3.1	Automated Sampler calibration:

Calibration is accomplished using a subroutine in the regular sampler program. At the prompt for
sample calibration in the routine place a graduated cylinder in the refrigerated sample compartment and
place the delivery tube end in the cylinder. Note the volume and respond to the program requests for
this information. The program will automatically adjust the pumping time to deliver the correct volume.
The program will prompt for a recheck of the volume with the new volumetric data you have entered.
Recheck the volume delivered as necessary and complete the program steps.

6.3.2	Calibration Frequency

The sampler shall be calibrated monthly to ensure that equal samples are drawn and that sufficient
sample volume is drawn for the necessary analysis sub-samples. The amount normally drawn for each
of the 15 samples is between 450 and 550 milliliters. This provides a total composite sample of between
6.75 and 8.25 liters.

6.4	Water Quality and Operational control Checks

6.4.1	Water Quality Data

Spiked samples for each method will be analyzed at the rate outlined in the BCDHE SOP and QA Plan
(Attachment III) and GAI QA Summary (Attachment II).

Method blanks will be analyzed at the rate outlined in the BCDHE SOP and QA Plan (Attachment III)
and GAI QA Summary (Attachment II).

Travel blanks will be provided to the BCDHE and GAI laboratories twice during the sample period.

Performance evaluation samples will be analyzed under the MA Department of Environmental
laboratory certification program at the rate of twice per annum.

6.4.2	Quality control for equipment operation

Laboratory analytical instruments shall be checked for accuracy based upon the SOP and QA plans for
the GAI and BCDHE laboratories (Attachments II and III).

All analytical and sampling equipment at the MA SSTC will be maintained and calibrated by MA SSTC
and BCDHE personnel according to the manufacturer's instructions and according to the MA SSTC
SOP (Attachment I).

6.5	Maintenance of Chain of Custody

6.5.1 COC Forms

Chain of custody forms (COC) shall be filled out in triplicate prior to sample transportation. If the person
transporting the samples is not the field sampler, the chain of custody form should indicate the transfer
of samples. Retain a copy of the COC for records.

Samples will be transported from MA SSTC to Barnstable County Health laboratory in coolers packed
with ice, immediately following completion of sample collection. Travel time to Barnstable County Health
should be less than one hour.

Samples to be subcontracted to the Groundwater Analytical laboratory will be included in the chain of
custody to the BCDHE laboratory. Subcontracted samples will be picked up from the BCDHE laboratory
and transported by Groundwater Analytical courier. Subcontract samples will be transported from
Barnstable County Health laboratory to the GAI laboratory in coolers packed with ice held at 4°C. Travel
time to GAI laboratory is approximately 45 minutes. A separate chain of custody will be created and
accompany subcontract samples to the GAI laboratory.

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BCDHE personnel in charge of sample intake and transfer to GAI laboratory shall maintain the chain of
custody for subcontracted samples and retain a copy of the chain of custody for project records.

6.5.2 Cooler receipts

Cooler receipts will be part of the chain of custody forms. The receipt will include the observed condition
of samples and the cooler temperature.

6.6 Acceptance Criteria

Analytical acceptance criteria for QA objectives for each matrix are listed in Table 5-1. The criteria are
contained in the Barnstable County Department of Health Laboratory Standard Operating Procedures
(SOP) available upon request. Calibration procedures for analytes measured at the Groundwater
Analytical, Inc. facility, are summarized in Attachment 2. Acceptance criteria for pH, temperature and
dissolved oxygen are discussed in MA SSTC SOP, Section 2.6, Attachment I.

6.6.1	Criteria for acceptance of Operational Facility Parameters

Influent wastewater dose volumes are calibrated weekly with a bucket test. Acceptance criteria for the
measurements shall be that the 30-day average volume of the wastewater delivered to the technology
shall be within 100% +/-10% of the systems rated hydraulic capacity. An exception to this volume shall
be during the Low Flow Stress Test when the 21-day average volumes accepted will be 100%+/-10%
of the daily reduced flow (50% of normal daily flow volume). For purposes of calculating the 21-day
average volume, only the 21 days of the Low Flow Stress period are to be included.

6.6.2	Criteria for acceptance of technology operational parameters

Electrical use is manually recorded from the dedicated electric meter and criteria are the meter reading,
and pertinent Field Log notations (date, time recorder's name). Accuracy of the meter as claimed by the
manufacturer shall be noted in the Field Log. The meter shall be returned to the manufacturer for
recalibration following the end of the Test Period and the recalibration results entered in the Field Log.

6.7	Assessment of additional QA Objectives (mass balance)

The use a mass balance approach to removal performance is not contemplated at this time.

6.8	Corrective Action Plan

6.8.1	Analytical methods

Corrective actions for analytical methods (listed in Table 5-1) performed at the BCDHE and GAI
laboratories are outlined in the BCDHE SOP and in the GAI QA summary (Attachments III and II). When
analytical parameters fall outside of the relevant acceptance criteria, corrective action will be taken to
rerun samples. Such actions may include: re-analysis of sample and standards; re-analysis with
appropriate fresh reagents and standards. Corrective action may also take the form of measures to
prevent future occurrence of the problem. Any problems with analysis will be noted in the relevant
laboratory log book and corrective actions taken will also be recorded in the laboratory log book..

6.8.2	Sample Collection. Handling and Field Measures

Corrective actions for field sampling and field analytical procedures at MA SSTC are included in the MA
SSTC SOP (Attachment I, Sections 1.4, and below)and in the performance evaluation audits outlined in
Section 9 below. Whenever necessary or appropriate, shortcomings in the execution of this test plan
revealed by audits will be corrected

Sample Collection

Nonconformance of sample collection with procedures in this Test Plan and the MA SSTC SOPS will be
noted in the Field Log. Likewise any corrective action taken will be recorded in the Field Log.
Nonconformance can include: automated sampler malfunction due to electrical fault; improperly
programmed sampler controller; failure to initiate sampler program; movement of suction line and loss
of suction. (Refer to MASSTC SOP Section 1.4).

Sample Handling

Nonconformance with sample handling and transport will be recorded in the Filed Log and any
corrective action taken recorded in the Field Log.

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Field Analytical Measurement

Nonconformance with field measures refers to measurement of Temperature, pH, and Dissolved
Oxygen made at the MA Septic System Test Center. Measurements that fall outside of the acceptance
criteria for these analyses will be noted in the Field Log. Corrective action shall be taken and noted in
the Field Log.

For pH, corrective actions can include: measurements with the pH meter which appear to be anomalous
can be repeated; buffers can be checked between measurements; sample duplicates are run at the
prescribed rate in this document; the meter can be recalibrated, or recalibrated with fresh buffers, and
the sample(s) reanalysed.

Temperature is measured with an separate thermistor probe, and subsequently measured with a
second thermistor on the pH probe. Corrective actions may include remeasurement of temperature.

Dissolved oxygen problems can include excessive drift during measurement; excessive temperature
shift during measurement; and failure to agitate probe sufficiently during measurement. When problems
with measurement occur, corrective actions may include: remeasurement; recalibration of the meter and
probe; replacement of meter batteries with fresh; and replacement of probe membrane. Measurements
that fall outside of the acceptance criteria for these analyses will be noted in the Field Log. Corrective
action shall be taken and noted in the Field Log.

6.9	Sample Cross contamination preventive measures

Composite sample containers shall be uniquely labeled with plastic tags attached with plastic wire ties
identifying the technology, and sample location. Composite sample bottles are thus dedicated to a
single technology and sampling point throughout the testing period. In the field facility, to minimize cross
contamination while processing analytical sub-samples and during field analytical measurements,
samples will be processed beginning with the most highly treated effluent, then intermediate effluent
and last the wastewater influent.

6.10	QA management structure

6.10.1	QA Manager
Thomas Bourne

Director, Water Quality Testing Laboratory

Barnstable County Department of Health and the Environment

Superior Court Bldg.

Barnstable, Ma 02640

508-375-6606

Responsibilities: QA Manager, Laboratory Director, Sample custody transfer between BCDHE
and GAI lab

Qualifications: Ph.D., chemistry. BCDHE Water quality lab director, 1993-present.

6.10.2	Project Participants

George Heufelder

Project Manager

Barnstable County Department of Health and the Environment
Superior Court Bldg.

Barnstable, Ma 02640
508-375-6616

Responsibilities: Overall Project Management, Data reduction, Report preparation, sample
transport

Qualifications: M.A., Biology; Environmental Programs Director, BCDHE, 1988-present

Sean Foss

MA Septic Sys tem Test Facility Operator

Barnstable County Department of Health and the Environment

Superior Court Bldg.

Barnstable, Ma 02640

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508-563-6757

Responsibilities: Operation of MA Septic Test Facility and wastewater dosing to technology,
Sample Collection, Sample Custody, Sample Field chemical, physical and process (O&M)
measurements, Data entry, Data reduction, reporting.

Qualifications: B.S. Zoology; Environmental Specialist BCDHE 1997-present.

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7.0 Reports and other deliverables

Table 7-1
Data Reporting Table

Parameter

Reporting Units

Matrix





Method





Influent

Intermediate*

Effluent



BODs

Milligrams/liter

X





Floppy Disk
Paper Table

CBODs

Milligrams/liter



X

X

Floppy Disk
Paper Table

Suspended Solids

Milligrams/liter

X

X

X

Floppy Disk
Paper Table

PH

pH units

X

X

X

Floppy Disk
Paper Table

Temperature

Degrees C.

X

X

X

Floppy Disk
Paper Table

Alkalinity

Milligrams/liter
(CaCOs)

X

X

X

Floppy Disk
Paper Table

Dissolved Oxygen

Milligrams/liter



X

X

Floppy Disk
Paper Table

TKN

Milligrams/liter

X

X

X

Floppy Disk
Paper Table

Ammonia as N

Milligrams/liter

X

X

X

Floppy Disk
Paper Table

Total Nitrite as N

Milligrams/liter



X

X

Floppy Disk
Paper Table

Total Nitrate as N

Milligrams/liter



X

X

Floppy Disk
Paper Table

Influent Wastewater

Gallons per day

X





Floppy Disk
Paper Table

7.1 Deliverables

The following are deliverables from BCDHE to NSFI:

7.1.1	Sampling Report

A Sampling Report of each sampling event during the evaluation period following all sampling activities. This
report will consist of a brief summary of the major actions performed, any problems encountered since the
previous report, and corrective actions taken to correct problems. This information will be kept in project files
along with the COC forms and the Field Log documenting the sampling activities.

7.1.2	Data Summary Report

A Data Summary Report consisting of tabulated summaries of the data including startup data will be provided
by BCDHE to the Verification Organization in both electronic and hard copy format. The summaries will show
the sample identifiers, the analyses performed, and the measured concentration or effects, including all
relevant qualifiers and validation flags. A brief narrative statement on the overall data quality and quantity will
also accompany the tabulated summaries. The BCDHE Project Manager will coordinate with the laboratory
project managerto define the format of these data summary reports. All data summary reports shall also be
forwarded to the Verification Organization Project Manager following review by the BCDHE Project Manager.

7.1.3	Operation and Maintenance Report

An Operation and Maintenance Report will be provided by BCDHE Project Manager or MA Test Facility
Operator of the operation and maintenance activities which were performed during the verification testing
period. The report will consist of a summary ofthe recommended operation and maintenance activities forthe
technology and any additional operation or maintenance tasks that were required during the test period. This

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report shall clearly delineate when the Waterloo Biofilter® Systems Inc. provided technical assistance to the
Testing Organization.

The Operation and Maintenance Report will also comment upon the WBS O&M manual as it relates to the 12
month operation and maintenance record of the WBS technology. Comments could include: maintenance
needed but not covered by the manual; clarification of the WBS O&M language, etc.

7.1.4 Quality Control and Analytical Report

A Quality Control and Analytical Report will be used to address the quality control practices employed during
the project. The report will also summarize the problems identified in the sampling reports, which are likely to
impact the quality of the data. The report will include:

1)The	project description, including report organization and background information

2)	Summaries of the sampling procedures, sample packaging, sample transportation, and decontamination
procedures at the MA Test Center.

3)	A summary of the GAI and BCDHE laboratory analytical methods, detection limits, quality control activities,
deviations from planned activities, and a summary of the data quality for each analysis and matrix.

4)	An assessment of the sampling and analyses techniques, an evaluation of the data quality of each
parameter, and an evaluation of the usability of the data.

5)	A summary of any field or analytical procedures that could be changed or modified to better characterize the
raw influent and treated effluent in future evaluations.

6)	An overall discussion of the quality of the environmental data collected during the evaluation and whether or
not it meets the project objectives.

7)	Identification of the QA samples which were split and sent to the GAI and BCDHE laboratories and to the QA
laboratory.

8)	All cooler receipt and COC forms associated with the required sample results.

9)	A laboratory case narrative to be included in the results if nonconformance or other evaluation events affect
the sample results.

10)	The portion of the primary field sample results and associated batch QC results, which conform to the QA
samples submitted to the QA laboratory.

7.2 Data Reduction

7.2.1	BCDHE Laboratory

Data reduction procedures for the BCDHE laboratory analysis of parameters are contained in the SOPS
(Attachment I) for each analyte/parameter.

7.2.2	GAI laboratory

Data reduction procedures for the GAI laboratory analysis of parameters are contained in the SOPS
(Attachment II) for each analyte/parameter.

7.2.3 MASSTC

Data reduction for influent flow calculations will be done by the MA Test Center Operator. The daily wastewater
flow into the technology will be derived and reduced based on the procedures outlined in the MA Test Center
SOPS included as Attachment I.

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8 Assessments

8.1	Audits at MASSTC

MA SSTC will conduct audits of dosing pump calibrations, sampling and sample processing on a quarterly
basis. For audits, a check list of operations performed will be created.

8.1.1	Dosing pumps

For the dosing pump calibrations the checklist will include calibration equipment set-up procedures, calibration
procedure, and logging of calibration results.

8.1.2	Sampling

For sampling the audit checklist will include composite container preparation, installation and retrieval, sampler
calibration check, and sampler programming.

8.1.3	Sample Processing

For sample processing the audit checklist will include the setup, calibration and measurement of pH and D.O.
meters, the measurement of temperature, the splitting of the composite sample into sub-sample containers,
use of the COC, and sample preservation and transport.

8.1.4	Responsible personnel

Personnel who are responsible for the above audits are: George Heufelder, BCDHE and Sean Foss, BCDHE.
Audits will be kept on file for reference by NSF.

8.2	Audits at BCDHE laboratory

BCDHE laboratory audits are regularly conducted by BCDHE personnel for each analytical method in the Test
Plan. Audits will be conducted by: Thomas Bourne, BCDHE.

8.3	Waste Management Plan

Liquid Waste

Liquid waste generated by the Testing Organization consists of: raw wastewater and process effluent from
sample collection; 2% dilute bleach (sodium hypochlorite); and small volumes of pH and conductivity
standards. These are disposed of into the sink and toilet drains at the test site. The effluent enters the facility
sewer system to be treated at the Air National Guard wastewater treatment plant. Liquid waste generated by
the Testing Organization does not enter or mix with the Test Facility influent wastewater.

Solid waste

Solid waste generated at the testing Organization consists of paper and cardboard and other packaging
materials. Disposal of these wastes are to the Upper Cape Regional Solid waste transfer plant. Residuals left
in the WBS septic tank and process tank are mixed (liquified) and pumped into the Test Facility sewerto be
treated at the Air National Guard wastewater treatment plant.

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