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Review on heterogeneous oxidation and adsorption for arsenic removal from drinking water

Journal of Environmental Sciences 2021年第12期33卷 178-188页

作者： Ruiping Liu Jiuhui Qu Key Laboratory of Drinking Water Science and Technology Research Center for Eco-Environmental SciencesChinese Academy of SciencesBeijing 100085China Center for Water and Ecology State Key Joint Laboratory of Environment Simulation and Pollution ControlSchool of EnvironmentTsinghua UniversityBeijing 100084China

The long term exposure of arsenic via drinking water has resulted in wide occurrence of arsenisim globally, and the oxidation of the non-ionic arsenite(As(Ⅲ)) to negatively-charged arsenate(As(Ⅴ)) is of crucial importance for the promising removal of arsenic. The chemical oxidants of ozone, chlorine, chlorine dioxide, and potassium permanganate may achieve this goal;however, their application in developing countries is sometimes restricted by the complicate operation and high cost. This review paper focuses on the heterogeneous oxidation of As(Ⅲ) by solid oxidants such as manganese oxide, and the adsorption of As(Ⅴ)accordingly. Manganese oxide may be prepared by both chemical and biological methods to achieve good oxidation performance towards As(Ⅲ). Additionally, manganese oxide may be combined with other metal oxides, e.g., iron oxide, to improve the adsorption capability towards As(Ⅴ). Furthermore, manganese oxide may be coated onto porous materials of metal organic frameworks to develop novel adsorbents for arsenic removal. To achieve the application in engineering works, the adsorbents granulation may be achieved by drying and calcination, agglomeration, and the active components may also be in situ coated onto the porous materials to maintain the oxidation and adsorption activities as much as possible. The novel adsorbents with heterogeneous oxidation and adsorption capability may be carefully designed for the removal of arsenic in household purifiers, community-level decentralized small systems, and the large-scale drinking water treatment plants(DWTPs).This review provides insight into the fundamental studies on novel adsorbents, the development of innovative technologies, and the demonstration engineering works involved in the heterogeneous oxidation and adsorption, and may be practically valuable for the arsenic pollution control globally.

关键词： Arsenic heterogeneous oxidation Adsorption Manganese oxide Drinking water

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heterogeneous reactions of SO_2 on ZnO particle surfaces

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Science China Chemistry 2011年第1期54卷 161-166页

作者： LI Jia,SHANG Jing & ZHU Tong State Key Joint Laboratory of Environmental Simulation and Pollution Control College of Environmental Sciences and Engineering,Peking University,Beijing 100871,China 1. State Key Joint Laboratory of Environmental Simulation and Pollution Control College of Environmental Sciences and Engineering Peking University Beijing 100871 China

heterogeneous reactions of SO2 on ZnO particle surfaces were studied using in situ diffuse reflectance infrared Fourier transform spectroscopy （DRIFTS）. The influences of relative humidity （RH） and UV radiation （2= 365 nm） were investigated. In the absence of UV radiation, sulfite was the prominent product on the particle surfaces, and a negative relationship between RH and sulfite production was observed. In the presence of UV radiation, infrared （IR） absorption of sulfite and sulfate was evident in the spectra. With increasing RH or UV intensity, sulfite was gradually transformed into sulfate. UV intensity and RH exhibited a synergistic effect on the heterogeneous oxidation of SO2 on ZnO. On dry particles and with no UV radiation, the reaction order of SO2 on ZnO particles was 1.6. The initial uptake coefficient for the formation of sulfite, using the Brunauer-Emmett-Teller （BET） area as the reactive surface area of SO2, was 4.87 × 10^-6. At 40% RH and with UV radiation, the reaction order was 0.91, and the initial uptake coefficient was 2.29 ×10^-5.

关键词： SO2 ZnO DRIFTS heterogeneous oxidation UV radiation

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A review of the direct oxidation of methane to methanol

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Chinese Journal of Catalysis 2016年第8期37卷 1206-1215页

作者：韩宝斋杨扬许妍妍 U.J.Etim 乔柯许本静阎子峰中国石油大学(华东)化学工程学院重质油国家重点实验室山东青岛266580

This article briefly reviewed the advances in the process of the direct oxidation of methane to methanol （DMTM） with both heterogeneous and homogeneous oxidation. Attention was paid to the conversion of methane by the heterogeneous oxidation process with various transition metal ox‐ides. The most widely studied catalysts are based on molybdenum and iron. For the homogeneous gas phase oxidation, several process control parameters were discussed. Reactor design has the most crucial role in determining its commercialization. Compared to the above two systems, aque‐ous homogenous oxidation is an efficient route to get a higher yield of methanol. However, the cor‐rosive medium in this method and its serious environmental pollution hinder its widespread use. The key challenge to the industrial application is to find a green medium and highly efficient cata‐lysts.

关键词： Methane Direct oxidation Methanol heterogeneous oxidation Gas-phase homogeneous oxidation Aqueous catalyzed oxidation

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