Laserfiche WebLink
Former Town& Country_Chevron -2- _ 1/23/98 <br /> F t. III L. 1 Y w i,-. aF µ <br /> San Joaquin County' - _: <br /> Y. <br /> xylene. Therefore, water in the vadose zone is leaching contamination from the soil at 7.5 to 9.0 ft bgs, <br /> and spreading the__rota—inationto'16'ft'bgs where-it is reabsorbed onto the soil above detectable levels" <br /> The soil data show a definite decreasing trend in the concentration of contaminants from the waste oil <br /> tank. Measurable amounts of petroleum contaminants probably occur in this water at depths greater than <br /> 16 ft bgs. However, the concentration of contaminants is too low to be absorbed onto the soil in <br /> measurable amounts.. Therefore;the concentration in the vadose zone water is probably too low to <br /> impact ground water(70 to 100 ft bgs). <br /> ' - ., �� .. , t -` <br /> .,t,� s . <br /> Soil samples were collected from the bottomz of the gasoline tank excavation at 13 - 14 ft bgs, and at 5 ft <br /> intervals while advancing the borings. The analytical results of these samples shows that contaminated <br /> soil remains from 13 ft bgs to greater than 26 ft bgs. At the bottom of the gasoline tanks, soil samples Y <br /> lad an average concentration of 553 mg/kg%TPH=g, 0.42 mg/kg benzene;79$ mg/kg toluene, 2.56 <br /> mg/kg ethylbenzene, and 34:80 mg/kg xylene: The samples were nondetect for lead and ethylene <br /> 200 mg/kg TPH- , 0.005 - 6.7 mg/kg <br /> dibromide. At 20 ft bgs contamination vanes from nondetect to 3, g g g _ _ <br /> benzene, nondetect to 32 mg/kg toluene, non detect to 58 mg/kg ethylbenzene, and 0.008=220 mg/kg <br /> xylene. The concentration of petroleum contaminants increases with depth within the sandy clay bed. <br /> One soil sample, collected from boring B-1 in the clayey sand layer at 29 ft bgs had 2.3 mg/kg TPH-g, <br /> 0.49 mg/kg benzene, 0.074 mg/kg toluene, 0.066 mg/kg ethylbenzene, and 0.24 mg/kg xylene. The <br /> increase in the concentration of contamination within the sandy clay bed at depth, indicates the original <br /> contamination may have extended through this clay bed to an unknown depth within the vadose zone or <br /> to the water table. Because petroleum contaminants do not adhere to sand and silt as readily as clay, <br /> water percolating through the vadose'zone would leach the petroleum contaminates from the sand and <br /> silt beds more readily than from the clay bed. This is'possibly'the reason the soil'sample from the'ciayey <br /> sand bed showed a significant decrease in the concentration of petroleum contaminants.- Yet, significant <br /> contamination may remain in deeper deposits where petroleum contaminants may have been absorbed <br /> onto the surface of the "saprolitic"bed or migrated through fractures in this bed and absorbed onto <br /> deeper'clay deposits. <br /> Conclusions: The extent of soil contamination beneath the waste oil tank has been determined: Soil <br /> contamination was detected in the deepest analyzed samples from borings, B-1 and B-5, and the <br /> concentration of contarr i ation increases-witlf-deptl within the sandy clay-bed: Therefore;'the extent-of.. <br /> contamination was not:determined beneath the gasoline tanks.' iL <br /> k Recommendations: The lateral and vertical extent of col tarrrination needs to Wdetermined beneath the <br /> gasoline tanks. Additional soil samples should be collected at 5 ft intervals or at lithologic changes from.. <br /> the depth of the last petroleum contaminated sample into and possibly through the "saprolitic".bed to the <br /> nearest clay bed. These samples should be analyzed for petroleum contanninants to determine the°4 <br /> vertical extent of contamination. if water is not encountered, a computer model (ex, VLEACH or <br /> SESOIL) and Waste Extraction Test (WET) or Toxicity Characteristic Leaching Procedure (TCLP)tests <br /> analyses are needed to determine the probability this contamination will impact groundwater. if water is <br /> encountered; samples should be collected and analyzed far'petroleum contaminants including methyl a <br /> tertiary-butyl ether(MTBE) and the other oxygenates using EPA`Method 8260. This additional <br /> information- is required to calculate the mass of contamination remaining on-site. ' ' - <br />