Reductive dechlorination of chlorinated hydrocarbons as non-aqueous phase liquid (NAPL): Preliminary investigation on effects of cement doses
Creators
- 1. Department of Chemical Engineering, Hanyang University, Seoul 133-791 (Korea, Republic of)
- 2. Zachry Department of Civil Engineering, Texas A and M University, College Station, TX 77843 (United States)
Description
The reactivities of various types of iron mixtures to degrade chlorinated hydrocarbons (PCE, TCE and 1,1,1-TCA) in the form of non-aqueous phase liquids were investigated. The iron mixtures included a mixture of Fe(II) and Portland cement (Fe(II)-C), a mixture of Fe(II), Fe(III) and Ca(OH)2 (Fe(II/III)-L), and a mixture of Fe(II), Fe(III), Ca(OH)2, and Portland cement (Fe(II/III)-C). When the same amount of Fe(II) was used, Fe(II)-C was more reactive with chlorinated ethylenes (i.e. PCE and TCE) than Fe(II/III)-L. The reductive pathway for high concentrations of total PCE (i.e. above solubility) with Fe(II)-C was determined to be a combination of two-electron transfer, β-elimination and hydrogenolysis. Increasing the cement dose from 5% to 10% in Fe(II)-C did not affect PCE dechlorination rates, but it did favor the β-elimination pathway. In addition, when Fe(II/III)-C with 5%C was used, PCE dechlorination was similar to that by Fe(II)-C, but this mixture did not effectively degrade TCE. A modified second-order kinetic model was developed and shown to appropriately describe degradation of TCE at high concentrations. Fe(II/III)-L effectively degraded high concentrations of 1,1,1-TCA at rates that were similar to those obtained with Fe(II)-C using 10% C. Moreover, both increasing cement doses and the presence of Fe(III) increased dechlorination rates of 1,1,1-TCA, which was mainly through the hydrogenolysis pathway. The reactivity of Fe(II/III)-L was strongly dependent on the target compound (i.e. less reactivity with TCE, more with 1,1,1-TCA). Therefore, Fe(II/III)-L could be a potential mixture for degrading 1,1,1-TCA, but it should be modified to degrade TCE more effectively. - Highlights: ► TCE yield indicated that PCE dechlorination was through hydrogenolysis and β-elimination. ► β-elimination, especially PCE to dichloroacetylene, was favored with the higher cement doses. ► Lower reactivity of Fe(II/III)-L was observed for dechlorination of TCE compared to other iron mixtures. ► Addition of Fe(III) and the additional cement doses in Fe(II)-C increased 1,1,1-TCA dechlorination.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2012.04.070Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2012.04.070;
- PII
- S0048-9697(12)00641-9;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 430
- Journal Page Range
- p. 82-87
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44116152
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- CALCIUM HYDROXIDES; CONCENTRATION RATIO; DECHLORINATION; ETHYLENE; IRON; ORGANIC CHLORINE COMPOUNDS; POLLUTION CONTROL; PORTLAND CEMENT; REACTIVITY
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; ALKENES; BUILDING MATERIALS; CALCIUM COMPOUNDS; CEMENTS; CHEMICAL REACTIONS; CONTROL; DEHALOGENATION; DIMENSIONLESS NUMBERS; ELEMENTS; HYDROCARBONS; HYDROGEN COMPOUNDS; HYDROXIDES; MATERIALS; METALS; ORGANIC COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; OXYGEN COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.