Overcoming Barriers to the Remediation of Carbon Tetrachloride Through Manipulation of Competing Reaction Mechanisms
Quantify the kinetics of all competing product-formation pathways, over a range of conditions relevant to groundwater remediation, using well-mixed batch reactors and analysis primarily by chromatography. At OGI, batch experiments were conducted on Fe(0) systems (both Fisher Electrolytic and Nano-sized iron). The experiments were done with and without buffer. The buffered experiments tried to contrast two buffers: an organic buffer (EPPS, presumably a H atom donor), and the inorganic borate. In the buffered experiments, the pH was varied (7.3 and 8.4). For the pre-exposure treatment, after trying a variety of methods, like shaking and not shaking for varied amounts of time, it was decided to stick with not shaking and have a pre-exposure of 24 hours. The unbuffered data did not show any marked trend with increasing mass of Felc. However, 3.5 g of Fe showed about 100% conversion to CHCl3, and 1g of Fe showed 50% conversion. At pHs 8.4 and 7.3, there was no trend observed for branching ratios between EPPS and Borate buffer. kCT (disappearance rate constant of carbon tetrachloride) values were found to be different from CT and CF fits. Experiments with nano-iron (unbuffered, buffered with both buffers at pH 8.3), did not show any trend with respect to Fisher Iron, except for the unbuffered experiments, where the CF ''yield'' was less in the nano iron case. Future experiments involve testing for chloride, formate and CO, and performing experiments over a wider range of pH and buffers. Batch experiments were conducted at PNNL to compare the efficiency and product distribution of representative Fe(II) and Fe(0) systems applied to dechlorination of CCl4. These experiments involved (1) a smectite clay with Fe(III) in its structure that had been reduced to Fe(II) by dithionite treatment, (2) the same clay to which Fe(II) was added as an exchangeable cation, (3) electrolytic Fe(0) from Fisher, and (4) a mixture of the reduced clay and Fe(0). Experiments were conducted in headspace vials at pH 7 in either bicarbonate or bis-tris propane buffers. Reactant and product concentrations were determined by headspace analysis using GC/MS. Results from the first run of this experiment showed relatively little dechlorination by the Fe(II) system, and from 50-80% dechlorination by the Fe(0) system after 48 h. Essentially no CHCl3 was seen in the Fe(II) system, whereas as 30% of the original CCl4 was converted to CHCl3 in the Fe(0) system. Very low amounts of CH2Cl2 were seen in all treatments. Plans are underway to repeat this experiment and use a cryo-GC capability that will allow simultaneous determination of CO as well as the chlorinated methanes. This is important because CO represents the end product of the second hypothetical dechlorination pathway that may compete with the CHCl3 pathway and will aid in mass balance calculations. An additional experiment to evaluate the Henry's Law constant for CCl4 in aqueous solutions in the presence and absence of clay showed no significant difference due to the presence of clay, although slightly higher gas-phase concentrations were seen when clay was present.
- Research Organization:
- OGI School of Science & Engineering, Beaverton, OR (US)
- Sponsoring Organization:
- USDOE Office of Science (SC) (US)
- DOE Contract Number:
- FG07-02ER63485
- OSTI ID:
- 836460
- Report Number(s):
- EMSP-86820A-2003; R&D Project: EMSP 86820; TRN: US200503%%640
- Resource Relation:
- Other Information: PBD: 1 Jun 2003
- Country of Publication:
- United States
- Language:
- English
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