EPA-670/4-75-005
ApriM975
Environmental Monitoring Series

-------

-------
                                               EPA-670/4-75-005
                                               April 1975
     INVESTIGATION OF THE ORION RESEARCH CYANIDE MONITOR
                              By

                     Robert J. O'Herron
Methods Development and Quality Assurance Research Laboratory
                 Program Element No. 1HA327
           NATIONAL ENVIRONMENTAL RESEARCH CENTER
             OFFICE OF RESEARCH AND DEVELOPMENT
            U.S. ENVIRONMENTAL PROTECTION AGENCY
                   CINCINNATI, OHIO  45268

-------
                     REVIEW NOTICE




The National Environmental Research Center—Cincinnati




has reviewed this report and approved its publication.




Mention of trade names or commercial products does not




constitute endorsement or recommendation for use.
                           11

-------
                             FOREWORD

Man and his environment must be protected from the adverse effects
of pesticides, radiation, noise and other forms of pollution, and
the unwise management of solid waste.  Efforts to protect the
environment require a focus that recognizes the interplay between
the components of our physical environment—air, water, and land.
The National Environmental Research Centers provide this multi-
disciplinary focus through programs engaged in

     •    studies on the effects of environmental
          contaminants on man and the biosphere, and

     •    a search for ways to prevent contamination
          and to recycle valuable resources.

This report is part of a continued effort by the Instrumentation
Development Branch, Methods Development and Quality Assurance
Research Laboratory (MDQARL), NERC-Cincinnati, to investigate
instruments and provide information to both users and suppliers.
The intention is also to upgrade instrumentation, and to make it
possible to choose the most suitable instrument for a particular
application.
                                 A. W. Breidenbach, Ph.D.
                                 Director
                                 National Environmental
                                 Research Center, Cincinnati
                               111

-------
                             ABSTRACT

The model 1206 Orion Research cyanide monitor was investigated
using the Orion specifications and environmental considerations as
a guide.  This is one of the Series 1000 monitors manufactured by
Orion which duplicate laboratory analyses made with ion-selective
electrodes.  The Series 1000 monitors perform single parameter
measurements of concentration, it is reported, and continuously
display the results on a panel meter and a strip chart recorder.
Sample pretreatment techniques are applied against an array of
interferences encountered in the use of ion-selective electrodes.
The cyanide monitor employs a silver/sulfide--sodium reference
electrode set in the indicator method to detect, continuously, the
level of cyanide in a sampled stream.  Cadmium, copper, nickel,
and zinc complexes of cyanide are broken by two reagents added in
the fluids-chemical section.  The breakdown of tightly bound
cyanide complexes of iron, cobalt, and platinum are not effected
by the addition of these reagents.  Hydrogen cyanide (HCN) is
converted to the free cyanide ion for detection by the electrodes.

Laboratory tests under controlled environmental conditions showed
the electronic stability  (drift) to be within 0.1% over the temper-
ature range of 5C to 35C.  Sensor stability, over the temperature
range 5C to 35C was tested by applying free cyanide ion (standard
solutions of 1 mg/1 and 10 mg/1) as direct input to the monitors.
The results of these tests showed that Orion's specified tolerance
of ±10% of reading was met.  Two out of three electrode sets tested
for linearity were within Orion's tolerance of ±0.02 ppm below 0.25
ppm and ±10% of readings above 0.25 ppm cyanide concentration.
Dynamic on-stream measurements were made from a metal plating pro-
cess rinse stream in a field installation of the monitor, and these
measurements were periodically compared with those of the standard
method for total cyanide.  This field installation revealed the
comparisons were widely variable.   Steady-state comparisons were
made of field-collected samples with the standard method for
determining total cyanide.  These tests revealed that a 15% to 20%
loss in cyanide concentration resulted from the required straining
and filtering of the sample input to the monitor.
                                 IV

-------
                             CONTENTS
Abstract                                                      iv
List of Figures and Tables                                     v
Acknowledgments                                               vi

Sections
I      Conclusions                                             1
II     Recommendations                                         4
III    Introduction                                            5
IV     The Orion Cyanide Monitor                               8
V      Laboratory Evaluation                                  11
VI     Field Evaluation                                       17
VII    Laboratory Tests with Field Sample                     22
VIII   References                                             24

                        FIGURES AND TABLES

Figure
Number

  1    Series 1000 Monitors                                    8
  2    Block Diagram of the Chemical Sensing Section          10
  3    Preamplifier Output Voltage--CTA Temperature
         Transistion from 45C to 30C                          14
  4    Fluid Connections to Monitor                           17
  5    Regression Line with 95% Confidence Limits for
         the Mean Response                                    21

Table
Number

  1    Ten Day Operation                                      11
  2    Environmental Tests with Continuous Measurement
         of Sample                                            13
  3    Linearity and Lower Limit Detection of Cyanide
         Standards                                            15
  4    Comparison of Cyanide Monitor Field Installation
         Data with Laboratory Analysis of Total Cyanide       20
  5    Relative System Response with Varying Pressure
         Input                                                22
  6    Laboratory Test with Cyanide Waste Samples Col-
         lected in the Field                                  23

-------
                          ACKNOWLEDGMENTS

We gratefully acknowledge the support and help of L.  B.  Lobring
(Physical and Chemical Methods Branch,  MDQARL) in preparing stan-
dards and analyzing samples; P. P. Kovatis (of the Metal Finishers
Foundation) in securing industry cooperation to permit the monitor
to be installed on a cyanide waste stream; R. P. Lauch (instrumen-
tation Development Branch, MDQARL) for contributing suggestions
that helped in selecting hydraulic test apparatus; and T.  J.
Stasiak and W. T. O'Connell (Orion representatives) for their
installation assistance and helpful suggestions throughout this
investigation.
                                 VI

-------
                             SECTION I

                            CONCLUSIONS

1.  Modification in components and procedures  made by Orion during
    the interval of this evaluation of  the cyanide monitor indi-
    cated the model tested was still in the prototype stage of
    development.

2.  Being in an early stage of production, some improvements in
    quality control of components appear to be necessary.

3.  Electronic drift at constant temperature (20C) was less than
    0.1% for a 1-week interval.

4.  Electronic drift over the temperature range 5C to 35C  was
    0.12%.

5.  Sensor drift over the temperature range 5C to 35C was  within
    Orion's specified tolerance of ±10% of reading for cyanide
    standards of 1 mg/1 and 10 mg/1. This occurs if the operation
    is within Orion's framework:  the constant temperature assem-
    bly is maintained 5C above ambient  temperatures of 25C and the
    automatic restandardization has taken place after the  tempera-
    ture change.

6.  Two of three electrode sets tested  were within Orion's toler-
    ance of ±0.02 ppm on concentrations below  0.25 ppm cyanide and
    ±10% of reading on concentrations above 0.25 ppm cyanide.  The
    other electrode set ranged slightly higher--to within  0.04 ppm
    on concentrations below 0.25 ppm cyanide.

7.  As a result of this investigation,  Orion has had the instruc-
    tion manual, which lacked clarity and depth, rewritten and
    broadened in scope.

8.  Data from the cyanide monitor installed in a field location
    varied widely from the standard method determinations  of total
    cyanide.  This variability was caused by:

        a.  an inability to maintain input pressure to the filter
            at the recommended 15 to 20 psi:  the strainer and
            a throttling value clogged  when the monitor was unat-
            tended,

-------
         b.   a drop in cyanide concentration across  the  strainer
             and filter,
         c.   an inability of the  monitor to  measure  total  cyanide,
             and
         d.   the long delay (8 to 10  minutes with  adequate pressure
             input) of fluids in  transit and of electrode  response
             dampened the abrupt  and  cyclic  variations in  cyanide
             concentrations of the wastewater sampled.   (Note:
             Discussions  with Orion personnel about  problems  en-
             countered in maintaining suitable pressure  input to
             the filter has resulted  in a new prefilter  design.)

 9.   Steady-state tests with field samples showed  that a 15%  to 20%
     loss in cyanide concentration occurred  across the strainer and
     filter.

10.   Essentially all of the cyanide passing  the filter was measured
     by the  monitor for these particular samples.   (Note:   This is
     sample  dependent.)

11.   Response time to a change in cyanide concentration  was a func-
     tion of the sample input pressure.

12.   As a result of the number of tests and  the length of time
     necessary to complete these  tests, there were no long-term
     tests made of the effectiveness  of either the electrodes (4
     month replacement) or the filter (1 month replacement).

13.   The monitor does not measure iron, cobalt, platinum,  gold, and
     silver  complexes of  cyanide.  Chlorine  is a negative  interfer-
     ence.  High levels of sulfide (10 mg/1  and above) cause  a
     positive interference and must be avoided. Orion continues
     its research effort  to counteract these interferences.

14.   In summary, the cyanide monitor  includes stable electronics
     that performed very  well over changing  environmental  condi-
     tions.   Ambient temperature  should be controlled, not to
     exceed  30C because high temperature reduces the life  of the
     electrodes.  Fluids  flow requires that  the temperature be
     controlled above OC.  The reference voltage feedback  techni-
     que employed in the  automatic restandardization approach is
     clever; it is effective in compensating for the long-term
     drift that's encountered in  the  use of ion-selective  elec-
     trodes.  Application of the  monitor should not  be considered

-------
routine.  Care and maintenance will be a continuing require-
ment.  Qualified personnel, aware of sample characteristics
and monitor limitations, are required to interpret the data;
i.e., qualified chemists should perform periodic comparison
tests with the standard method for total cyanide.   The monitor
measures some of the loosely bound metal cyanide complexes,
but not those which are tightly bound.  The presence and the
effect of other interferences, e.g., chlorine and sulfide, on
the electrode signal output should be known.

-------
                            SECTION II

                          RECOMMENDATIONS

The Orion cyanide monitor does not measure total cyanide,  and
problems were encountered with its use.   However, the standard
method for measuring total cyanide cannot be performed rapidly,
unattended, inexpensively, continuously,  or with few problems.
Each method performs capably in some category.   Therefore, it is
recommended that the desirable qualities  of each be utilized to
their fullest extent.  The cyanide monitor cannot measure  total
cyanide, but with care and proper maintenance,  it can measure
some forms of the cyanide present in certain wastes.   And  Orion
is planning future improvements.  At present, the cyanide  monitor
can be used where continuous surveillance is required on wastes
suspected of having excessive cyanide.  Dual set-point,  high-
and low-alarm limits, included in the monitor,  can be employed
to actuate a sampling device when a predetermined limit  has been
exceeded.  Thus, samples can be screened  in the field so that the
time-consuming analysis of the standard method for total cyanide
can be expedited.  If it can be shown that positive interfer-
ences are not present, gross violations  of effluent standards as
indicated by a calibrated and functional  monitor, should be use-
ful.

The Orion Series 1000 monitors are designed and developed  to meet
needs of Industry.  As a result of these  developments, as  in the
case of the cyanide monitor, these instruments  could also  be of
use to EPA procurements provided the application and performance
requirements are well defined.

-------
                            SECTION III

                           INTRODUCTION

Ion-selective electrodes developed within the past two decades
have been employed with instrument systems under favorable process
conditions for control purposes.  Generally, these instruments were
utilized as indicators of gross process upsets.  The mere presence
of a measured parameter could be indicative of a breakdown at some
point within a process.  In these earlier process control applica-
tions of ion-selective electrodes, pretreatment of the sample has
primarily involved obtaining favorable pH and controlling the
temperature.  These instrument systems measured sample parameters
under favorable process conditions and performed useful control
functions in industrial processes.  That is, the uncomplexed, free
ion was measured in samples where interferences were known to be
minimal.

In recent years, several manufacturers have made a concerted effort
to use continuous monitors for concentration values of parameters.
Interferences encountered with the use of ion-selective electrodes
make it necessary to pretreat the sample in monitoring systems.
The interferences can be due to the sample itself or to the
measuring electrode and the reference electrode.  Ion-selective
electrodes respond to the free, unbound ion, not the total concen-
tration of a chemical species.  Increased use of ion-selective
electrodes in laboratory analyses over the years has resulted in
methods being developed to free bound ions so that concentrations
can be determined.  Ions resulting in electrode interferences
must be either removed or avoided through chemical pretreatment
techniques.  The amount and type of other ions in solution (ionic
strength)* affect the signal output of ion-selective electrodes.
The activity, a, of an ion is related to the concentration, C, by
the equation

        a = YC                                                (1)

where y is the activity coefficient, which is dependent upon the
total ionic strength of the solution.  Ionic strength adjusters
(ISA) are available that when added to standardizing solutions and
samples, "swamp out" differences so that the activity coefficient
of the ion being sensed is about the same in all solutions.

The pH of the sample may also result in interferences:  bound ions

-------
may be decomplexed at a favorable pH or interfering ions may be
preferentially complexed within a certain pH range.  In addition,
either the hydrogen (H+) or hydroxyl (OH~) ions may be an elec-
trode interference.  Therefore, sample pH adjustment is a usual
requirement.

The voltage output of ion-selective electrodes is characterized by
the Nernst equation at constant temperature.

        E = E° + (0.19841T/n) log a.                         (2)


The variation as a result of temperature change is described by
T. S. Light.2

        dE/dT = dE°/dT + (0.19841/n) log a. +

        (0.19841T/n)(d log a^dT)                            (3)


Sample temperature affects not only the Nernstian slope term
[(0.19841/n) log ajj , but also the "solution temperature coeffi-
cient" term [0.19841T/n)(d log ai/dT)].  Light has discussed the
solution temperature coefficient term:

        "The activity of an ion may be affected by its
        activity coefficient and for weak or complex
        forming electrolytes by its equilibrium rela-
        tionships.  Since activity coefficients and
        equilibrium constants may each have tempera-
        ture coefficients of their own, the 'solution
        temperature coefficient' term may become quite
        complex."

Because temperature compensation techniques normally correct for
the Nernst slope term only, temperature control of the sample is
generally selected by Orion.  Sample color and turbidity do not
interfere with the voltage relationships in the use of ion-
selective electrodes.  Filtering is necessary, however, to combat
clogging of tubing or fouling of electrodes.

In regard to reference electrodes, Orion has stated, "Our experi-
ence over the past several years has shown that most of the
problems that users of specific ion electrodes have reported to
us are directly traceable to the liquid junction in the external
reference electrode."3  Requirements for 0.1 to 0.2 mv accuracy

-------
for 1% to 2% ion activity, as opposed to approximately 6 mv to
obtain 0.1 pH unit accuracy, were indicated.  These tougher re-
quirements for specific ions have led Orion to advise using a
second specific ion electrode,4 as a reference electrode--one
whose level can be kept constant.

-------

-------