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ARCHIVED REPORTS_XR0012663
Environmental Health - Public
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2900 - Site Mitigation Program
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PR0507217
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ARCHIVED REPORTS_XR0012663
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Last modified
6/23/2020 4:53:26 PM
Creation date
6/23/2020 2:20:09 PM
Metadata
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Template:
EHD - Public
ProgramCode
2900 - Site Mitigation Program
File Section
ARCHIVED REPORTS
FileName_PostFix
XR0012663
RECORD_ID
PR0507217
PE
2950
FACILITY_ID
FA0007741
FACILITY_NAME
AUTO ZONE INC
STREET_NUMBER
1100
Direction
N
STREET_NAME
WILSON
STREET_TYPE
WAY
City
STOCKTON
Zip
95202
APN
11733035
CURRENT_STATUS
02
SITE_LOCATION
1100 N WILSON WAY
P_LOCATION
01
QC Status
Approved
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and with decafluorotriphenylphosphine (DFTPP) for semi- <br /> volatile analyses to determine adequate ion abundance. Once <br /> the systems are calibrated and tuned, analysis and quality <br /> control measures follow those procedures outlined in the <br /> general requirements above. <br /> Compounds analyzed by gas chromatography are tentatively <br /> identified by comparing retention times of the sample and the <br /> standard. Retention time windows are based on ± 3 standard <br /> deviations from the average of 3 injections of a particular <br /> analyte over a 72 hour period. Linder certain conditions, <br /> tentatively identified compounds must be confirmed on a <br /> second column of different affinity. Sample quantitation <br /> procedures are outlined in each method. Method detection <br /> limits are quantified according to SW-846 Chapter 1, Revision <br /> 1, December 1987. All calculations and instrumentation <br /> parameters are documented in the analysts' notebook. <br /> Inorganics - Metals and Wet Chemistry <br /> Appropriate procedures for sample extraction, preparation, <br /> and clean-up are referenced in the individual methods in SW- <br /> 846 1986 and the 1987 revision as well as in "Standard <br /> Methods for the Examination of Water and Wastewater" 16th <br /> Edition 1985, and are followed accordingly. <br /> In addition to the general requirements lis'ted above, each <br /> analyte must have a calibration curve calculated from a <br /> reagent blank and three higher concentrations of the analyte <br /> that define the linear quantitation range for that analyte. <br /> Each concentration, including the reagent blank, must be <br /> analyzed 3 times and the average used to determine the <br /> calibration curve. The %RSD must be <15% for the curve to be <br /> considered linear through the orig�i. The $RSD's, the <br /> calibration curve, and the calculations from the triplicate <br /> analysis of the four calibration concentrations are <br /> documented in the analysts' notebook. The curve is verified <br /> at least once daily and must be within lot of the original <br /> line. The verification is documented in the analyst's <br /> notebook. Standards used to establish the calibration curves <br /> are renewed quarterly. All calculation and instrumentation <br /> parameters are kept in the analyst's notebook. <br /> Bacteriology/Bioassay <br /> _ The bacteriology department adheres to the quality control <br /> measures set out in EPA-600/8--78-017 December 1978 "Microbial <br /> Methods for Monitoring the Environment". Because bacterial <br /> analyses are ill suited to the internal duality control <br /> measures required of other analyses, they are subject to <br /> strict external requirements. <br /> - <br /> 12 <br />
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