A comparison of the dechlorination mechanisms and Ni release styles of chloroalkane and chloroalkene removal using nickel/iron nanoparticles
2016
Zhang, Wei | Jia, Nan | Han, Xiaolin | Qiu, Zhaofu | Lv, Shuguang | Lin, Kuangfei | Ying, Weichi
In this study, we compared the removal kinetics and Ni release styles of 1,1,1-trichloroethane (1,1,1-TCA), trichloroethylene (TCE), and tetrachloroethene (PCE) that result from the use of Ni/Fe nanoparticles in water. Compared to TCE and PCE, 1,1,1-TCA was more readily removed, and the concentration profiles of the three chlorinated aliphatic hydrocarbons (CAHs) during the reduction processes fit pseudo-first-order reaction rate models well. The surface area-normalized rate constants show that the 11% Ni Ni/Fe nanoparticles, which has the largest Brunauer–Emmett–Teller surface area, has the highest capacity for 1,1,1-TCA removal per unit surface area and that the 6% Ni sample was the best for removing TCE and PCE. The observed by-products suggested that hydrogenolysis was responsible for the dechlorination of CAHs in the presence of Ni/Fe nanoparticles. More Ni2+ was released during the degradation of 1,1,1-TCA than that of TCE and PCE because Ni will reduce the CAHs directly as a zerovalent metal does when hydrogen atoms in the Ni lattice are not sufficient due to the rapid incomplete dechlorination of 1,1,1-TCA. The different modes of adsorption of chloroalkane and chloroalkene onto the surfaces of Ni/Fe particles might play an important role in their dechlorination process.
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