Degradation of Tetrachloroethylene and Trichloroethylene under Thermal Remediation Conditions

Thermal;Trichloroethylene;Tetrachloroethylene;Degradation

Costanza, Jed ; Civil and Environmental Engineering

University:Georgia Institute of Technology

Department:Civil and Environmental Engineering

关键词: Thermal;    Trichloroethylene;    Tetrachloroethylene;    Degradation;   

Others  :  https://smartech.gatech.edu/bitstream/1853/7485/1/costanza_jed_200512_phd.pdf.pdf

美国|英语

来源: SMARTech Repository

【 摘 要 】

Thermal remediation involves heating subsurface environments and collecting fluids in order to recover contaminants such as tetrachloroethylene (PCE) and trichloroethylene (TCE). While increasing subsurface temperature can lead to changes in the distribution of contaminants between the solid, liquid, and gas phases, there is also an increased potential for PCE and TCE to degrade. This work was performed to determine the rate of PCE and TCE degradation and products formed in laboratory-scale experiments designed to simulate thermal remediation conditions. The conditions during transport of gas-phase TCE were simulated using flow-through experiments in the temperature range from 60 to 800C. Degradation of TCE was not evident at temperatures of less than 240C; however, chloroacetic acids, which comprised less than 0.1% of the influent TCE on a carbon basis, were detected. At temperatures greater than 300C, TCE readily degraded where the identities of the degradation products were a function of oxygen and water content. With oxygen present, TCE degraded to form CO, phosgene, CO2 with minor amounts of hexachloroethane, PCE, and carbon tetrachloride. Increasing the amount of water vapor was found to decrease the amount of TCE degraded. Vapor recovery systems used during thermal treatments are anticipated to capture these TCE degradation products. However, the amount of missing carbon (~17%) in experiments completed at 800C makes the prospect of recovering all TCE degradation products doubtful. Experiments were conducted using hermetically sealed ampules to simulate heating dissolved phase PCE and TCE over periods of up to 75 days. At 120C, the first-order TCE degradation half-life was 330 days and the degradation products included CO and CO2, glycolate, formate, and chloride. The rate of TCE disappearance was increased with the addition of 1% (wt.) goethite, which suggests that the presence of iron bearing soil minerals can increase rates of TCE degradation during thermal treatment. In contaminated field samples, TCE was found to degrade to form cis-1,2-dichloroethylene at 95C coincident with the formation of hydrogen gas. Degradation of PCE was not evident in field samples or in deionized water and is not expected to degrade during thermal remediation at temperatures below 95C.