Products compositions and release rates from intense thermal treatment of soil

被引:21
作者
Bucala, V
Saito, H
Howard, JB
Peters, WA
机构
[1] MIT,ENERGY LAB,DEPT CHEM ENGN,CAMBRIDGE,MA 02139
[2] MIT,CTR ENVIRONM HLTH SCI,CAMBRIDGE,MA 02139
关键词
D O I
10.1021/ie9505726
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Yields, compositions, and global release rates of major products from heating a synthetic soil matrix under conditions pertinent to current and emerging thermal remediation technologies are reported. The soil specimens were mixtures prepared for the U.S. EPA to reflect certain attributes of soils from U.S. Superfund sites. Because this study focuses on determining how soil decomposition itself may affect thermal cleanup, exogenous contaminants were not added to the soil. The experiments involved heating 49-54 mg batches of 63-125 mu m neat soil particles, thinly spread on a 0.001 in. thick stainless steel foil, at nominal rates of 1000 degrees C/s, to temperatures in the 350-1050 degrees C range, under 3 psig of helium. Above 500-600 degrees C the total weight loss increased strongly with increasing temperature. Devolatilization exceeded 21 wt % when soil was heated to 1033 degrees C and then maintained at this temperature for 5 s before cooling. For this heating regimen, CO2, CO, and tars were the major volatile products, material and carbon balances were good, but oxygen balances were only fair and hydrogen balances were poor, possibly because yields of chemical water were not quantified. A single first-order reaction kinetics model well describes the global release rates of most gaseous volatiles except CO2, which, because of apparent step-like evolution, is better fitted by a model consisting of two independent parallel first-order reactions. A multiple independent parallel first-order reaction kinetics model provides a good fit to the soil weight loss data.
引用
收藏
页码:2725 / 2734
页数:10
相关论文
共 38 条
[1]  
ANTHONY DB, 1975, 15TH S INT COMB PITT, P1303
[2]   USE OF LANGMUIR METHOD FOR KINETIC STUDIES OF DECOMPOSITION REACTIONS - CALCITE (CACO3) [J].
BERUTO, D ;
SEARCY, AW .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1974, 70 :2145-2153
[3]  
BONNEAU M, 1982, CONSTITUENTS PROPERT
[4]  
BRINDLEY GW, 1987, CHEMCLAYS CLAY MINER, pCH7
[5]   THE CALCINATION OF DOLOMITE .1. THE KINETICS OF THE THERMAL DECOMPOSITION OF CALCITE AND OF MAGNESITE [J].
BRITTON, HTS ;
GREGG, SJ ;
WINSOR, GW .
TRANSACTIONS OF THE FARADAY SOCIETY, 1952, 48 (01) :63-69
[6]   THERMAL-TREATMENT OF FUEL OIL-CONTAMINATED SOILS UNDER RAPID HEATING CONDITIONS [J].
BUCALA, V ;
SAITO, H ;
HOWARD, JB ;
PETERS, WA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1994, 28 (11) :1801-1807
[7]   ANALYSIS OF DIFFUSION AND SORPTION OF CHLORINATED HYDROCARBONS IN SOIL BY SINGLE-PELLET MOMENT TECHNIQUE [J].
CABBAR, C ;
DOGU, G ;
DOGU, T ;
MCCOY, BJ ;
SMITH, JM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1994, 28 (07) :1312-1319
[8]  
*EPA, 1989, DEV US EPA SYNTH SOI
[9]   RESULTS OF TREATMENT EVALUATIONS OF A CONTAMINATED SYNTHETIC SOIL [J].
ESPOSITO, P ;
HESSLING, J ;
LOCKE, BB ;
TAYLOR, M ;
SZABO, M ;
THURNAU, R ;
ROGERS, C ;
TRAVER, R ;
BARTH, E .
JAPCA-THE JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 1989, 39 (03) :294-304
[10]  
Gerhartz W, 1985, ULLMANNS ENCY IND CH, VFifth