在不同pH值的溶液中,催化剂表面吸附的物质种类不同。在酸性条件下,催化剂表面主要吸附氢,催化剂表面为还原态,吸附的H+可以促进NHQ+的进一的英语翻译

在不同pH值的溶液中,催化剂表面吸附的物质种类不同。在酸性条件下,催化

在不同pH值的溶液中,催化剂表面吸附的物质种类不同。在酸性条件下,催化剂表面主要吸附氢,催化剂表面为还原态,吸附的H+可以促进NHQ+的进一步生成;在中性和碱性条件下不利于NHQ+的生成,可能由于随着溶液pH的升高NHQ+自身分解,氨以非离子NH:的形式存在更易于被氧化。在碱性条件下,催化剂表面主要吸附氧化物(如OH,OH一和Ox-),表面为氧化态,这些氧化物占据了催化剂的活性中心,与硝酸盐产生了竞争吸附,且pH越高,覆盖率越高,硝酸盐还原活性明显下降。Abdallah R等[oat用多孔铜电极作为阴极电解硝酸盐,实验发现硝酸盐在中性溶液中的还原产物大部分为氨氮,氨氮选择性最高达96 %,在酸性溶液中氨氮浓度明显降低,且在中性溶液中的电流效率明显高于在酸性溶液中。Maria Dort-siou等[35]对6种金属电极(Sn, Bi, Ph, Al, Zn, Ir>)电化学还原N03一的反应速率和产物组成进行了研究,认为Bi是水处理中最有前景的金属电极。pH>4时,主要产物是Nz, NZO ,氨和亚硝酸盐;pH为0-4时,主要产物是氨和轻胺。
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结果 (英语) 1: [复制]
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In solutions with different pH values, the types of substances adsorbed on the catalyst surface are different. Under acidic conditions, the surface of the catalyst mainly adsorbs hydrogen, and the surface of the catalyst is in a reduced state. The adsorbed H + can promote the further generation of NHQ +; it is not conducive to the formation of NHQ + under neutral and alkaline conditions, which may be due to the increase in pH with the solution NHQ + decomposes on its own, and ammonia is more easily oxidized in the form of nonionic NH :. Under alkaline conditions, the surface of the catalyst mainly adsorbs oxides (such as OH, OH, and Ox-), and the surface is in an oxidized state. These oxides occupy the active center of the catalyst, which competes with nitrate for adsorption, and the higher the pH , The higher the coverage, the nitrate reduction activity decreased significantly. Abdallah R et al. [Oat used a porous copper electrode as the cathode to electrolyze nitrate. The experiment found that most of the reduction products of nitrate in neutral solution were ammonia nitrogen, the selectivity of ammonia nitrogen was up to 96%, and the concentration of ammonia nitrogen in acid solution was significantly reduced, and The current efficiency in neutral solutions is significantly higher than in acidic solutions. Maria Dort-siou et al. [35] studied the reaction rate and product composition of the electrochemical reduction of NO3 by 6 kinds of metal electrodes (Sn, Bi, Ph, Al, Zn, Ir>). Foreground metal electrode. When pH> 4, the main products are Nz, NZO, ammonia and nitrite; when the pH is 0-4, the main products are ammonia and light amine.
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结果 (英语) 2:[复制]
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In different pH-value solutions, the type of material adsorptioned on the surface of the catalyst was different. Under acidic conditions, the catalyst surface mainly absorbs hydrogen, the catalyst surface is reduced state, the adsorption of H-plus can promote the further generation of NHQ plus, in neutral and alkaline conditions is not conducive to the generation of NHQ, may be due to the increase of the solution pH NHQ plus self-decomposition, ammonia in the form of non-ion NH: the presence of more easily oxidized. Under alkaline conditions, the main adsorption oxides (e.g. OH, OH1 and Ox-) on the surface of the catalyst surface are oxidized, which occupy the active center of the catalyst, compete with nitrates for adsorption, and the higher the pH, the higher the coverage, the decrease in nitrate reduction activity. Abdallah R and other .oat using porous copper electrodeas as cathode electrolytic nitrates, the experiment found that most of the reductive products of nitrate in the neutral solution were ammonia nitrogen, ammonia nitrogen selectivity of up to 96 percent, the concentration of ammonia nitrogen in the acidic solution was significantly reduced, and the current efficiency in the neutral solution was significantly higher than in the acidic solution. Maria Dort-siou and others have studied the reaction rate and product composition of six metal electrodes (Sn, Bi, Ph, Al, Zn, Ir) electrochemical lyse N03, and considerbi to be the most promising metal electrode in water treatment. At pH 4, the main products are Nz, NZO, ammonia and nitrite, and at pH 0-4, the main products are ammonia and light amine.
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结果 (英语) 3:[复制]
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In the solution with different pH value, the adsorbed substances on the catalyst surface are different. Under acidic condition, hydrogen is mainly adsorbed on the surface of catalyst, and the surface of catalyst is reduced state. The adsorbed H + can promote the further formation of nhq +; under neutral and alkaline conditions, it is not conducive to the formation of nhq +. It is possible that ammonia is more easily oxidized in the form of non-ionic NH: due to the self decomposition of nhq + with the increase of solution pH. In the alkaline condition, the surface of catalyst mainly adsorbs oxides (such as Oh, oh - and ox -), which occupy the active center of catalyst and compete with nitrate. The higher the pH is, the higher the coverage is, the lower the reduction activity of nitrate is. Abdallah R et al. [oat used porous copper electrode as cathode to electrolyze nitrate. It was found that most of the reduction products of nitrate in neutral solution were ammonia nitrogen, and the selectivity of ammonia nitrogen was as high as 96%. The concentration of ammonia nitrogen in acid solution was significantly reduced, and the current efficiency in neutral solution was significantly higher than that in acid solution. Maria DORT Siou et al. [35] studied the reaction rate and product composition of electrochemical reduction of n03-1 by six kinds of metal electrodes (SN, Bi, pH, Al, Zn, IR >), and considered that BI was the most promising metal electrode in water treatment. When pH > 4, the main products are NZ, NZO, ammonia and nitrite; when pH is 0-4, the main products are ammonia and light amine.<br>
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