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DYNAMICS OF HYDROGEN SUPPLY AND DEMAND FOR IN SITU DEHALORESPIRATION

机译:原位除湿的氢供需动力学

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The diffusive release of hydrogen (H2) was evaluated as part of a multitechnology pilot program to evaluate the feasibility of various electron donors and delivery methods for reducing chlorinated hydrocarbons in groundwater at a former industrial facility in California. The evaluation was performed as part of a one-year pilot program using separate in-situ test cells designed to intercept treatment-zone groundwater. Groundwater flowing into the two test cells used for this study contained a mixture of chlorinated hydrocarbons, where trichloroethene (TCE) was the most abundant with initial average concentrations exceeding 50 milligrams per liter (mg/L). Sulfate was an important competing electron acceptor, where average pre-test concentrations were approximately 500 mg/L. Waterloo EmittersTM were installed in the test cells to deliver molecular hydrogen (H2) and sulfur hexafluoride (SF6) tracer gas to treatment zone groundwater by a passive, diffusive mechanism. Stoichiometric calculations revealed that the amount of H2 required for reducing TCE and sulfate greatly exceeded its aqueous solubility. Methods to overcome H2 solubility by increasing the H2 utilization rate included adding nutrients and implementing mechanical mixing of groundwater in both test cells. Hydrogen transfer rates were controlled by varying the partial pressure inside the emitters. In both test cells, results were similar, where a 4-fold reduction in TCE, and similar increase in cisdichloroethene (cDCE) concentration was observed over the evaluation period. Hydrogen sulfide increased and sulfate concentrations also decreased. Dissolved H2 concentrations inside both test cells remained below 60 nanomolar for most of the study, although numerical simulations and co-released SF6 tracer concentrations confirmed that the emitters were functioning as designed, and that sufficient H2 was being added to the system to explain the observed changes in TCE and sulfate concentrations. These results suggest that H2 solubility limitations were avoided because of rapid utilization by sulfatereducing and dechlorinating bacteria. More importantly, this work suggests that amendment utilization and supply rates are important considerations when designing insitu systems, and that stoichiometric considerations based on concentration data alone can be misleading when considering in-situ treatment options.
机译:作为一项多技术试验计划的一部分,评估了氢的扩散释放(H2),以评估各种电子供体的可行性以及在加利福尼亚州以前的一家工业设施中减少地下水中氯代烃的输送方法。该评估是为期一年的试验计划的一部分,使用了专门设计为拦截处理区地下水的独立现场测试池。流入用于本研究的两个测试池中的地下水包含氯化碳氢化合物的混合物,其中三氯乙烯(TCE)含量最高,初始平均浓度超过50毫克每升(mg / L)。硫酸盐是一种重要的竞争性电子受体,其平均测试前浓度约为500 mg / L。将Waterloo EmittersTM安装在测试单元中,以通过被动扩散机制将分子氢(H2)和六氟化硫(SF6)示踪气体输送到处理区地下水。化学计量计算表明,还原TCE和硫酸盐所需的H 2量大大超过其水溶性。通过提高H2利用率来克服H2溶解度的方法包括添加营养物并在两个测试单元中进行地下水的机械混合。通过改变发射器内部的分压来控制氢的传输速率。在两个测试单元中,结果相似,在整个评估期内,TCE降低了4倍,顺二氯乙烯(cDCE)浓度也得到了相似的提高。硫化氢增加,硫酸盐浓度也降低。尽管数值模拟和共释放的SF6示踪剂浓度证实发射器按设计工作,并且向系统中添加了足够的H2以解释所观察到的现象,但在大多数研究中,两个测试单元内的H2溶解浓度均保持在60纳摩尔以下。 TCE和硫酸盐浓度的变化。这些结果表明,由于硫酸盐还原和脱氯细菌的快速利用,避免了H2溶解度的限制。更重要的是,这项工作表明,在设计原位系统时,修正利用率和供应率是重要的考虑因素,而仅考虑浓度数据的化学计量因素在考虑原位处理方案时可能会产生误导。

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