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Catalytic decomposition of hydrogen peroxide and 4-chlorophenol in the presence of modified activated carbons

化学 活性炭 催化作用 吸附 过氧化氢 分解 氧化剂 化学分解 无机化学 激进的 水溶液 反应速率常数 零电荷点 核化学 动力学 有机化学 物理 量子力学
作者
Hsu-Hui Huang,Ming‐Chun Lu,Jong‐Nan Chen,Cheng-Te Lee
出处
期刊:Chemosphere [Elsevier BV]
卷期号:51 (9): 935-943 被引量:155
标识
DOI:10.1016/s0045-6535(03)00042-0
摘要

The objective of this research was to examine the heterogeneous catalytic decomposition of H(2)O(2) and 4-chlorophenol (4-CP) in the presence of activated carbons modified with chemical pretreatments. The decomposition of H(2)O(2) was suppressed significantly by the change of surface properties including the decreased pH(pzc) modified with oxidizing agent and the reduced active sites occupied by the adsorption of 4-CP. The apparent reaction rate of H(2)O(2) decomposition was dominated by the intrinsic reaction rates on the surface of activated carbon rather than the mass transfer rate of H(2)O(2) to the solid surface. By the detection of chloride ion in suspension, the reduction of 4-CP was not only attributed to the advanced adsorption but also the degradation of 4-CP. The catalytic activity toward 4-CP for the activated carbon followed the inverse sequence of the activity toward H(2)O(2), suggesting that acidic surface functional group could retard the H(2)O(2) loss and reduce the effect of surface scavenging resulting in the increase of the 4-CP degradation efficiency. Few effective radicals were expected to react with 4-CP for the strong effect of surface scavenging, which could explain why the degradation rate of 4-CP observed in this study was so slow and the dechlorination efficiency was independent of the 4-CP concentration in aqueous phase. Results show that the combination of H(2)O(2) and granular activated carbon (GAC) did increase the total removal of 4-CP than that by single GAC adsorption.

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