The Agency recognizes that there are certain circumstances where it is necessary to
filter or centrifuge a sample under controlled laboratory conditions prior to analysis to prevent
instrument damage. Sample filtration in the laboratory is permissible if insoluble materials
(e.g., silicates) remain after acid digestion of the sample, which could damage laboratory
equipment. If this step is necessary, the filter and the filtering apparatus should be thoroughly
cleaned and pre rinsed with dilute nitric acid. Laboratory personnel should refer to Chapter
Three of the EPA publication "Test Methods for Evaluating Solid Waste" (SW 846) for
information concerning these procedures.
The Agency also realizes that data generated from unfiltered samples may result in
higher concentrations of metals detected in ground water samples at some facilities. Because
background samples also will be unfiltered, however, false indications of contamination
should be minimized. In all cases, owners and operators should ensure that all samples used
in a statistical test are collected using the same procedures.
Ground water sampling that is conducted to perform ion balance calculations or to
classify ground water according to the amount of dissolved ions is not addressed in this
Chapter, because these analyses are not part of the Subpart F requirements. Scientific studies
that are performed to estimate aqueous concentrations of dissolved geochemical parameters
have different data objectives than Subpart F ground water monitoring, and commonly utilize
other techniques and procedures to achieve the desired research goals.
7.4
In Situ or Field Analyses
Physically or chemically unstable analytes should be measured in the field, rather than
in the laboratory. Examples of unstable parameters include pH, redox potential, dissolved
oxygen, and temperature. Although the specific conductance (i.e., electrical conductance) of a
sample should be relatively stable, the Agency recommends that this analyte also be measured
in the field. The Agency suggests that dissolved oxygen, turbidity, and specific conductance
be determined in the field as soon as practicable after the well has been purged. Most
conductivity instruments require temperature compensation; therefore, the temperature of the
samples should be measured at the time conductivity is determined unless the monitoring
equipment automatically makes this compensation.
Three methods are generally employed for measuring unstable parameters. The two
preferred methods are to use either an in line flow cell or specially designed analytical
equipment that has probes that may be lowered down into the well. These methods provide
results that typically are more precise than those obtained using the third method, collecting
discrete samples and analyzing them at land surface. Specifically, the third method involves
collecting a sample in a clean bottle or beaker in the same manner that a sample for
laboratory analysis would be collected, and then analyzing the sample using a field test kit or
meter at land surface. If down hole probes (e.g., pH electrode, thermistor) are used to
measure unstable parameters, the probes should be decontaminated in a manner that prevents
November 1992
7 22






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