Chlorinated ethene reduction by cast iron: Sorption and mass transfer

被引:86
作者
Burris, DR
Allen-King, RM
Manoranjan, VS
Campbell, TJ
Loraine, GA
Deng, BL
机构
[1] USAF, Res Lab, MLQR, Tyndall AFB, FL 32403 USA
[2] Washington State Univ, Dept Geol, Pullman, WA 99164 USA
[3] Washington State Univ, Dept Pure & Appl Math, Pullman, WA 99164 USA
[4] Appl Res Associates Inc, Tyndall AFB, FL USA
[5] New Mexico Inst Min & Technol, Dept Mineral & Envir Engrg, Socorro, NM 87801 USA
来源
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE | 1998年 / 124卷 / 10期
关键词
D O I
10.1061/(ASCE)0733-9372(1998)124:10(1012)
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Tetrachloroethylene (PCE) and trichlorethylene (TCE) exhibited significant nonlinear sorption to nonreactive sites when exposed to four cast irons. Cast iron is a reactive material that promotes reductive dechlorination and has recently been used for in-situ remediation of chlorinated solvent contaminated ground water. Comparisons between PCE sorption to cast iron, graphite, and iron-containing minerals indicate that nonreactive sorption is due to exposed graphite inclusions in the cast iron. Sorption of the homologous series of chloroethenes to a cast iron adheres to Traube's rule; thus, the extent of sorption is related primarily to compound hydrophobicity. An analytical model incorporating rate-limited sorption/desorption to nonreactive sites was used to assess sorption nonequilibrium Effective sorption and desorption rate coefficients determined how significant mass transfer limitations to nonreactive sorption sites exist for PCE and not for TCE. The nonreactive sorption observed indicates that how-through cast iron treatment systems will exhibit significant delayed attainment of steady-state conditions for chlorinated ethenes, particularly PCE and TCE.
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页码:1012 / 1019
页数:8
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