Azizian Mohammad F, Semprini Lewis
School of Chemical, Biological and Environmental Engineering, 116 Johnson Hall, Oregon State University, Corvallis, OR 97331, United States.
School of Chemical, Biological and Environmental Engineering, 116 Johnson Hall, Oregon State University, Corvallis, OR 97331, United States.
J Contam Hydrol. 2017 Aug;203:93-103. doi: 10.1016/j.jconhyd.2017.07.002. Epub 2017 Jul 6.
The simultaneous anaerobic transformation of tetrachloroethene (PCE) and carbon tetrachloride (CT) was evaluated in a continuous flow column. The column was packed with quartz sand and bioaugmented with the Evanite culture (EV) that is capable of transforming PCE to ethene. Azizian and Semprini (2016) reported that PCE and CT could be simultaneously transformed in the column, with PCE (0.1mM) transformed mainly to ethene and CT (0.015mM) to chloroform (CF) (20%) and an unknown transformation product, likely carbon dioxide (CO). The fermentation of propionate, formed from lactate fermentation, was inhibited after the transformation of CT, likely from the exposure to CF. Reported here is the second phase of that study where a second bioaugmentation of the EV culture was made to reintroduce a lactate and propionate fermenting population to the column. Effective lactate and propionate fermentation were restored with a H concentration of 25nM maintained in the column effluent. PCE (0.1mM) was effectively transformed to ethene (98%) and vinyl chloride (VC) (~2%). Unlabeled CT (0.015 to 0.03mM) was completely transformed with a transient build-up of CF and chloromethane (CM), which were subsequently removed below their detection limits. A series of transient tests were initiated through the addition of carbon-13 labeled CT (CT), with concentrations gradually increased from 0.03 to 0.10mM. GC-MS analysis of the column effluent showed that C labeled CO (CO) was formed, ranging from 82 to 93% of the CT transformed, with the transient increases in CO associated with the increased concentration of CT. A modified COD analysis indicated a lesser amount of CT (18%) was transformed to soluble products, while CO represented 82% the CT transformed. In a final transient test, the influent lactate concentration was decreased from 1.1 to 0.67mM. The transformation of both CT and PCE changed dramatically. Only 59% of the CT was transformed, primarily to CF. CO concentrations gradually decreased to background levels, indicating CO was no longer a transformation product. PCE transformation resulted in the following percentage of products formed: cDCE (60%), VC (36%), and ethene (4%). Incomplete propionate fermentation was also observed, consistent with the build-up of CF and the decrease in H concentrations to approximately 2nM. The results clearly demonstrate that high concentrations of CT were transformed to CO, and effective PCE dehalogenation to ethene was maintained when excess lactate was fed and propionate was effectively fermented. However, when the lactate concentration was reduced, both PCE and CT transformation and propionate fermentation were negatively impacted.
在连续流柱中评估了四氯乙烯(PCE)和四氯化碳(CT)的同步厌氧转化。该柱填充有石英砂,并用能够将PCE转化为乙烯的埃瓦尼特培养物(EV)进行生物强化。阿齐西安和森普里尼(2016年)报告称,PCE和CT可在柱中同时转化,PCE(0.1mM)主要转化为乙烯,CT(0.015mM)转化为氯仿(CF)(20%)和一种未知的转化产物,可能是二氧化碳(CO)。由乳酸发酵形成的丙酸盐发酵在CT转化后受到抑制,可能是由于接触了CF。本文报道的是该研究的第二阶段,对EV培养物进行了第二次生物强化,以便将能够发酵乳酸和丙酸盐的菌群重新引入柱中。当柱流出物中H浓度维持在约25nM时,有效恢复了乳酸和丙酸盐发酵。PCE(0.1mM)有效地转化为乙烯(约98%)和氯乙烯(VC)(约2%)。未标记的CT(0.015至0.03mM)完全转化,CF和氯甲烷(CM)有短暂积累,随后在检测限以下被去除。通过添加碳-13标记的CT(CT)启动了一系列短暂试验,其浓度从0.03逐渐增加到0.10mM。柱流出物的气相色谱-质谱分析表明,形成了C标记的CO(CO),占转化的CT的82%至93%,CO的短暂增加与CT浓度的增加相关。改进的化学需氧量分析表明,较少比例的CT(18%)转化为可溶性产物,而CO占转化的CT的82%。在最后一次短暂试验中,进水乳酸浓度从1.1降至0.67mM。CT和PCE的转化都发生了显著变化。只有59%的CT被转化,主要转化为CF。CO浓度逐渐降至背景水平,表明CO不再是转化产物。PCE转化产生的产物百分比为:顺式二氯乙烯(cDCE)(60%)、VC(36%)和乙烯(4%)。还观察到丙酸盐发酵不完全,这与CF的积累以及H浓度降至约2nM一致。结果清楚地表明,当供给过量乳酸且丙酸盐有效发酵时,高浓度的CT转化为CO,并且维持了PCE有效脱卤生成乙烯。然而,当乳酸浓度降低时,PCE和CT的转化以及丙酸盐发酵都受到负面影响。