Fallahpour Noushin, Yuan Songhu, Rajic Ljiljana, Alshawabkeh Akram N
Civil and Environmental Engineering Department, Northeastern University, Boston, MA, 02115, USA.
Civil and Environmental Engineering Department, Northeastern University, Boston, MA, 02115, USA; State Key Lab of Biogeology and Environmental Geology, China University of Geosciences, Wuhan, 430074, PR China.
Chemosphere. 2016 Feb;144:59-64. doi: 10.1016/j.chemosphere.2015.08.037. Epub 2015 Sep 5.
Palladium-catalytic hydrodechlorination of trichloroethylene (TCE) by cathodic H2 produced from water electrolysis has been tested. For a field in-well application, the flow rate is generally high. In this study, the performance of Pd-catalytic hydrodechlorination of TCE using cathodic H2 is evaluated under high flow rate (1 L min(-1)) in a circulated column system, as expected to occur in practice. An iron anode supports reduction conditions and it is used to enhance TCE hydrodechlorination. However, the precipitation occurs and high flow rate was evaluated to minimize its adverse effects on the process (electrode coverage, clogging, etc.). Under the conditions of 1 L min(-1) flow, 500 mA current, and 5 mg L(-1) initial TCE concentration, removal efficacy using iron anodes (96%) is significantly higher than by mixed metal oxide (MMO) anodes (66%). Two types of cathodes (MMO and copper foam) in the presence of Pd/Al2O3 catalyst under various currents (250, 125, and 62 mA) were used to evaluate the effect of cathode materials on TCE removal efficacy. The similar removal efficiencies were achieved for both cathodes, but more precipitation generated with copper foam cathode (based on the experiments done by authors). In addition to the well-known parameters such as current density, electrode materials, and initial TCE concentration, the high velocities of groundwater flow can have important implications, practically in relation to the flush out of precipitates. For potential field application, a cost-effective and sustainable in situ electrochemical process using a solar panel as power supply is being evaluated.
对通过水电解产生的阴极氢气进行钯催化三氯乙烯(TCE)加氢脱氯反应进行了测试。对于现场井下应用,流速通常较高。在本研究中,在循环柱系统中,在高流速(1 L min⁻¹)下评估了使用阴极氢气进行钯催化TCE加氢脱氯的性能,这是实际应用中预期会出现的情况。铁阳极可维持还原条件,并用于增强TCE加氢脱氯反应。然而,会发生沉淀现象,因此评估了高流速以尽量减少其对该过程的不利影响(电极覆盖、堵塞等)。在流速为1 L min⁻¹、电流为500 mA以及初始TCE浓度为5 mg L⁻¹的条件下,使用铁阳极时的去除效率(96%)显著高于混合金属氧化物(MMO)阳极(66%)。在Pd/Al₂O₃催化剂存在的情况下,使用两种类型的阴极(MMO和泡沫铜)在不同电流(250、125和62 mA)下评估阴极材料对TCE去除效率的影响。两种阴极实现了相似的去除效率,但泡沫铜阴极产生了更多沉淀(基于作者所做的实验)。除了电流密度、电极材料和初始TCE浓度等众所周知的参数外,地下水的高流速可能具有重要影响,实际上与沉淀物的冲洗有关。对于潜在的现场应用,正在评估一种使用太阳能电池板作为电源的经济高效且可持续的原位电化学工艺。