Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.4.23.17 (PCE)
 1,301 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The influence of residual cosolvent on the partitioning tracer technique for estimating a nonaqueous phase liquid (NAPL) saturation in porous media was investigated. Batch equilibrium and column miscible displacement tests were used to evaluate the influence of residual alcohol cosolvents in the aqueous phase on partitioning and transport of alcohol tracers through sandy soil columns containing tetrachloroethylene (PCE). As the volume fraction of cosolvent alcohol (f(c)) increased ( f(c) < or = 0.1; 10 vol %), partition coefficients (K(nc)) for the alcohol tracers linearly decreased for residual cosolvent ethanol, linearly increased for residual cosolvent tert-butyl alcohol, and did not exhibit an evident change for residual cosolvent 2-propanol. These observations are consistent with measured changes in solubility (S(c)) of the alcohol tracers over the same range (f(c) < or = 0.1) of these residual cosolvent alcohols. Column miscible displacement tests using ethanol as a residual cosolvent ( f(c) < or = 0.1) exhibited earlier partitioning tracer breakthrough leading to an underestimation of NAPL saturation (S(n)) when constant, cosolvent-free partitioning coefficients were assumed. The underestimation magnitude increased with higher initial residual cosolvent alcohol in the columns. The S(n) underestimates were not significant but were 1-10% lower than the actual S(n) (0.18). The estimated partition coefficients based on column tests with residual cosolvent (K(col)) were consistently less than those based on batch tests. Column tests with low (0.5%) and high (15%) S(n) revealed that the residual cosolvent alcohol effect was different depending on the amount of NAPL in the column. Using ethanol for a cosolvent (10%) and 2,4-dimethyl-3-pentanol as a partitioning tracer, the S(n) values were underestimated by about 17% and 5%, respectively, in the low and high NAPL saturation columns.
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PMID:Residual alcohol influence on NAPL saturation estimates based on partitioning tracers. 1273 48

The ability of modified Fenton reactions to promote simultaneous chemical and biological oxidation in an artificially contaminated soil was studied in batch laboratory slurry reactors. Tetrachloroethene (PCE) and oxalate (OA) were used to distinguish chemical oxidation from aerobic heterotrophic metabolism. PCE was mineralized by Fenton reactions, but OA was not oxidized. Indigenous soil microorganisms did not degrade added PCE aerobically but readily assimilated OA. Fenton reactions were promoted at the natural soil pH (7.6) by adding H2O2 and Fe(III), with nitrilotriacetic acid (NTA) as a chelator, at a constant molar ratio of H2O2/Fe(III)/NTA of 50:1:1. The *OH-mediated mineralization of PCE was demonstrated by adding 2-propanol (an *OH scavenger), which inhibited PCE oxidation. In subsequent dosing studies, PCE oxidation served as an indicator of Fenton reactions, while OA assimilation, dissolved oxygen (DO) concentration, and heterotrophic plate counts were indicators of aerobic microbial activity. Increasing Fenton doses to 20 times that required to achieve 95% PCE oxidation only delayed OA assimilation by 500 min and reduced plate counts by 1.5 log units g(-1) soil. Results show that aerobic metabolism can coexist with Fenton oxidation in soils.
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PMID:Effect of Fenton reagent dose on coexisting chemical and microbial oxidation in soil. 1668 23

The use of calcium peroxide (CaO2) powder as a source of H2O2 to promote modified Fenton (MF) chemistry was studied. First, the rate of production and yield of H2O2 from CaO2 dissolving in water at pH 6-9, and 12-13 (i.e., unbuffered CaO2) was measured. The rate of CaO2 dissolution increased as pH decreased, from 62 h for complete dissolution at pH 12-13 to only 4h at pH 6. The yield of H2O2 also increased with decreasing pH, from zero at pH 12-13 to 82% at pH 6. The ability of CaO2 to promote MF oxidation of PCE was demonstrated with a hydroxyl radical (OH) scavenger (2-propanol) at pH 8. The scavenger inhibited PCE oxidation, but 97% of the PCE was oxidized without it. Release of Cl(-) showed that PCE was mineralized. Finally, PCE oxidation was compared with liquid H2O2 (pH 7) and with CaO2 (pH 6, 7, 8, 9). Liquid H2O2 showed the lowest efficiency (mol H2O2 consumed/mol PCE oxidized) and the greatest temperature increase, disproportionation to O2, and PCE volatilization. CaO2 was a more efficient oxidant than liquid H2O2 at all pH values because it only releases H2O2 upon dissolution, reducing the loss to O2 and volatilization. CaO2 performed optimally at pH 8.
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PMID:Calcium peroxide (CaO2) for use in modified Fenton chemistry. 1780 64