非均相fenton类催化的活性炭改性。

P Compton, N R Dehkordi, P Larese Casanova, A N Alshawabkeh
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引用次数: 0

摘要

通过高级氧化工艺有效和高效地降解持久性、顽固性污染物对于减少有害废物和修复受污染的水域至关重要。其中一种高级氧化工艺是使用芬顿化学,可以使用多相催化剂进行优化。然而,为了使这种AOP优于传统的处理方法,需要从技术和经济的角度对该技术进行优化。从多相催化剂优化的角度来看,改变活性炭的表面化学性质,浸透或掺杂类芬顿催化纳米材料,可以消除芬顿化学中传统铁类相关的沉淀并发症,同时产生有效量的高氧化羟基自由基。采用多种工艺合成以活性炭为骨架的多相催化剂,在H2O2存在下,对羟基自由基的形成和苯甲酸的去除进行了测试。通过对各种添加剂的比较,在H2O2存在下,以5% MnO2浸渍的生活性炭可以实现高浓度的羟基自由基形成,同时保持较低的成本和相对容易的合成。该AC-Mn5催化剂在不同浓度的H2O2中表现良好,采用各种合成技术,模拟催化剂结构老化后,在较宽的pH范围内,酸性pH值下自由基形成最高。利用这种催化材料作为与传统Fenton技术相关的铁的替代品,设计一套完整的氧化功能,以实现持久、顽固的污染物去除,同时保持成本效益和可扩展性。预计这些催化材料能够有效地去除类似的污染物和混合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis.

Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis.

Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis.

Activated Carbon Modifications for Heterogeneous Fenton-Like Catalysis.

The effective and efficient degradation of persistent, recalcitrant pollutants by advanced oxidation processes is vital to both reduce hazardous waste and remediate polluted waters. One such advanced oxidation process is the use of Fenton chemistry, which can be optimized using heterogeneous catalysts. However, to make this AOP viable over conventional treatment methods, the technology needs to be optimized from both a technical and economic standpoint. From a heterogeneous catalyst optimization perspective, varying the surface chemistry of activated carbon and impregnating or doping with Fenton-like catalytic nanomaterials removes precipitation complications associated with traditional iron species in Fenton chemistry while generating effective amounts of highly oxidative hydroxyl radicals. Utilizing various techniques to synthesize heterogeneous catalysts with activated carbon as a backbone, in the presence of H2O2 the formation of hydroxyl radicals and removal of benzoic acid is tested. Comparing various additives, raw activated carbon impregnated with 5% MnO2 in the presence of H2O2 realized a high concentration of hydroxyl radical formation while maintaining low cost and relative ease of synthesis. This AC-Mn5 catalyst performed effectively in varying concentrations of H2O2, utilizing various synthesis techniques, after simulated aging of the catalyst structure, and over a wide pH range with the highest radical formation at acidic pH values. Utilizing this catalytic material as a substitute for iron species associated with traditional Fenton technology, the goal of designing a full set of oxidation functions towards persistent, recalcitrant pollutant removal while maintaining cost-effectiveness and scalability is proposed. It is anticipated these catalytic materials are effective to eliminate analogous contaminants and mixtures.

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