Insights into the contrasting effects of sulfidation on dechlorination of chlorinated aliphatic hydrocarbons by zero-valent iron.

Contrasting effects of sulfidation on contaminants reduction by zero-valent iron (ZVI) has been reported in literature but the underlying mechanisms remain unclear. Here, under well-controlled conditions, we compared the performance of ZVI and sulfidated ZVI (S-ZVI) toward a series of chlorinated compounds. Results revealed that, although S-ZVI was more reactive than ZVI toward hexachloroethane, pentachloroethane, tetrachloroethylene, and trichloroethene, sulfidation hindered the dechlorination of the other ten tested chlorinated aliphatics by a factor of 1.5-125. Moreover, S-ZVI may lead to an accumulation of toxic partially-dechlorinated products. Analogous to its effects on ZVI reactivity, sulfidation also exerted positive, negligible, or negative effects on the electron efficiency of ZVI. Solvent kinetic isotope effect analysis suggested that direct electron transfer rather than reaction with atomic hydrogen was the dominant reduction mechanism in S-ZVI system. Hence, the sulfidation enhancing effects could be expected only when direct electron transfer is the preferred reduction route for target contaminants. Furthermore, linear free energy relationships analysis indicated one-electron reduction potential could be used to predict the transformation of chlorinated ethanes by S-ZVI, whereas for chlorinated ethenes, their adsorption properties on S-ZVI determined the dechlorination process. All these findings may offer guidance for the decision-making regarding the application of S-ZVI.

Porous Indium Tin Oxide-Supported NiFe LDH as a Highly Active Electrocatalyst in the Oxygen Evolution Reaction and Flexible Zinc-Air Batteries.

The oxygen evolution reaction (OER) is crucial for hydrogen production from water splitting and rechargeable metal-air batteries. However, the four-electron mechanism results in slow reaction kinetics, which needed to be accelerated by efficient catalysts. Herein, a hybrid catalyst of novel nickel-iron layered double hydroxide (NiFe LDH) on porous indium tin oxide (ITO) is presented to lower the overpotential of the OER. The as-prepared NiFe LDH@ITO catalyst showed superior catalytic activity toward the OER with an overpotential of only 240 mV at a current density of 10 mA/cm2. The catalyst also offered high stability with almost no activity decay after more than 200 h of chronopotentiometry test. Furthermore, the applications of NiFe LDH@ITO in (flexible) rechargeable zinc-air batteries exhibited a better performance than commercial RuO2 and can remain stable in cycling tests. It is supposed that the superior catalytic behavior originates from the ITO conductive framework, which prevents the agglomeration and facilitates the electron transfer during the OER process.

Short-term and long-term effects of Zn (II) on the microbial activity and sludge property of partial nitrification process.

Autotrophic nitrogen removal was an innovative and economical nitrogen removal technology with less oxygen and no organics consumption, in which partial nitrification (PN) is the key component. It is necessary to clear the impact of metal ions on PN since the development of industry increased their opportunity for entering into wastewater. In this study, PN process was successfully started-up in an SBR, the short-term and long-term effects of Zn (II) on microbial bioactivity and the sludge adsorption ability for Zn (II) were investigated. Results suggested that low Zn (II) were favorable for AOB bioactivity, while the long-term effect also induced NOB bioactivity. The suppression threshold of Zn (II) on AOB in short-term effect was 10mgL-1, which rose to 50mgL-1 in the long-term effect due to the self-adaption. The PN sludge presented prominent absorbability for zinc and performed a quadratic relation with the Zn (II) concentration.