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24 August 2001 <br /> • AGE-NC Project No 98-0448 <br /> Page 3 of 7 <br /> 3 1 SOIL VAPOR EXTRACTIONIIN-SITU AIR SPARGE SYSTEM PROCEDURES <br /> Between 16 April 2001 and 30 June 2001, the SVE and IAS remediation systems were operational <br /> at the site The SVE system utilized a model Fuji, 3-horsepower regenerative vacuum blower and <br /> two 55-gallon carbon canisters to extract and adsorb hydrocarbon vapor from the subsurface Two- <br /> inch diameter, schedule 80 PVC piping was installed underground from wells VW-1 through VW-5 <br /> to the inlet of the regenerative vacuum blower, the outlet from the vacuum blower was routed <br /> through two sequential 55-gallon carbon canisters A Magnehelic vacuum gauge was attached to the <br /> inlet of the blower, air flow was monitored at the inlet using a Dwyer DS-200 flow sensor A flow <br /> rate was determined from the measured differential pressure and the piping diameter using a <br /> nomograph(Appendix B) The SVE air flow at the influent and effluent was monitored routinely for <br /> the presence of organic vapor using an organic vapor analyzer (OVA) equipped with a photo- <br /> ionization detector (PID Thermo Environmental 580A, 10 0 eV, calibrated to zsobutylene) <br /> Sampling ports were installed upstream of the vacuum blower inlet to recover SVE influent air flow <br /> vapor stream samples, and downstream of the vacuum blower to recover effluent SVE air flow <br /> samples to monitor the efficiency of hydrocarbon destruction Field measurements were recorded <br /> at regular intervals between 16 April and 30 June 2001 and are summarized in Table 5 <br />� i <br /> 3 2 COLLECTION AND ANALYSIS OF VAPOR EXTRACTION AIR FLOW SAMPLES <br /> Between 16 April and 30 June 2001, a total of ten extracted air flow vapor samples were collected <br /> from the influent and effluent of the regenerative vacuum blower unit to measure concentrations of <br /> hydrocarbon vapor The samples were collected in Tedlar bags using a hand air-vacuum pump <br /> Following sample collection, the samples were placed in a covered container and transported under <br /> chain-of-custody to either McCampbell Analytical Laboratory (MAL) in Pacheco, California or <br /> Precision Enviro-Tech (PET) in Stockton, California Each sample was analyzed,within 72 hours <br /> of collection for TPH-g and BTEX in accordance with-EPA Methods 5030/8015 Modified and 8020 <br /> r <br /> T- 4.0. FINDINGS -_ - - I - -- - - - -- - _ - - - _ r —, <br /> AGE determined ground water flow direction and gradient from the field data collected on 23 April <br /> 2001, the contaminant impact to ground water was assessed from the laboratory data <br /> From field data collected at the SVE remediation system between 16 April and 30 June 2000, AGE <br /> determined the average TPH-g concentration, the average flow rate and calculated the approximate <br /> mass and volume of hydrocarbons removed <br /> iAdvanced GeoE nviron mental,Inc <br /> I <br />