A novel nZVI-bentonite nanocomposite to remove trichloroethene (TCE) from solution

被引:31
作者
Baldermann, Andre [1 ]
Kaufhold, Stephan [2 ]
Dohrmann, Reiner [2 ,5 ]
Baldermann, Claudia [3 ]
Letofsky-Papst, Ilse [4 ]
Dietzel, Martin [1 ]
机构
[1] Graz Univ Technol, Inst Appl Geosci, Rechbauerstr 12, A-979 Graz, Austria
[2] BGR, Stilleweg 2, D-30655 Hannover, Germany
[3] Graz Univ Technol, Inst Technol & Testing Bldg Mat, Inffeldgasse 24, A-8010 Graz, Austria
[4] Graz Univ Technol, Inst Electron Microscopy & Nanoanal, Steyrergasse 17, A-8010 Graz, Austria
[5] LBEG, State Author Min Energy & Geol, Stilleweg 2, D-30655 Hannover, Germany
关键词
Chlorinated hydrocarbons; Nanoscale zero valent iron; Environmental pollution; Groundwater; Heavy metals; Bentonite clay; ZERO-VALENT IRON; MICROBIAL REDUCTION; AQUEOUS-SOLUTION; DECHLORINATION; REMEDIATION; PARTICLES; PATHWAYS; REACTIVITY; EFFICIENCY; TRANSPORT;
D O I
10.1016/j.chemosphere.2021.131018
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nanoscale zero-valent iron (nZVI) based (nano)composites supported by clay mineral substrates are a promising technology for the in-situ remediation of groundwater and (sub)soils contaminated with chlorinated hydrocarbons, such as trichloroethene (TCE). However, the physicochemical processes and interaction mechanisms between nZVI particles, clay minerals and TCE are poorly understood, yet. We immobilized nZVI particles on a commercial bentonite substrate to prepare a novel nZVI-B nanocomposite and tested its performance for TCE removal from solution against pure nZVI in batch reactors. The nZVI-B exhibited a higher reactivity (2.2.10(-3) L h(-1).m(2)) and efficiency (94%) for TCE removal than nZVI (2.2.10(-4) L h(-1).m(2); 45%). Sorption of TCE onto the clay surfaces and reductive de-chlorination in "micro-reactors" developing within the nZVI-B controlled the kinetics and the magnitude of TCE loss from solution. Contrary to pure nZVI, no signs of nZVI particle agglomeration or inactivation due to oxide shell formation were found in nZVI-B. We attribute this to the uptake of dissolved Fe species that are liberated via progressing nZVI particle corrosion by the bentonite substrate to form Fe-smectite (nontronite domains), which prevented from a deterioration of the properties and reactivity of the nZVI-B. The use of nZVI-B in permeable reactive barriers at contaminated field sites could be feasible, where a system-inherent reduction of the soil-bearing capacity has to be minimized.
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页数:9
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