首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >A novel combination of oxidative degradation for benzotriazole removal using TiO2 loaded on (FeFe2O4)-Fe-II-O-III@C as an efficient activator of peroxymonosulfate
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A novel combination of oxidative degradation for benzotriazole removal using TiO2 loaded on (FeFe2O4)-Fe-II-O-III@C as an efficient activator of peroxymonosulfate

机译:使用TiO2在(FeFE2O4)-Fe-II-OII-III @ C作为过氧键硫酸盐的有效活化剂的TiO2(FeFe2O4)-Fe-II-O-III-III-III-III-III-III-III-III-III-III-III-C的新组合

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摘要

A heterogeneous photocatalyst, TiO2-functionalized magnetic activated carbon (T@MPAC), was fabricated as a novel peroxymonosulfate (PMS) activator for improving the oxidative degradation of benzotriazole (BTA) in aqueous media. For characterization of the features of the synthesized catalyst, XRD, FESEM, EDS, BET, TEM, PL and UV-vis DRS techniques were applied. Influence of operating parameters namely solution pH, reaction time and catalyst dosages, PMS and BTA was studied in a batch environment. A plausible oxidation mechanism and reaction pathway for BTA degradation was proposed. Potential catalytic, recyclability, durability and quenching studies were performed. The catalytic activity of T@MPAC in the activation of different oxidants also evaluated. Under optimized conditions, the degradation and mineralization rates of BTA were found to be 71.6 and 38.7%, respectively, after the fifth cycles. The catalytic activity of T@MPAC on BTA degradation was improved with the suitability in order of PMS > persulfate > ozone > H2O2. The trapping experiments confirmed the participation of center dot OH, SO4 center dot-, O-2-center dot radicals as reactive species in the system. Among the reactive species (i.e. center dot OH, SO4 center dot-, O-2 center dot- and holes) included in T@MPAC/PMS/UV system, SO4 center dot- radicals had dominant role in controlling the oxidation reaction. Decreasing the degradation rate in the presence of scavenger agents was as IPA > BQ> t-BuOH>KI. The catalytic performance dropped in the presence of chloride ions, while it was less affected by phosphate, nitrate and sulfate anions. The catalyst showed a good recyclability and stability after five consecutive uses. To conclude, coupling of T@MPAC/UV and PMS can be successfully applied as a novel and effective technique to degrade organic substances in wastewater, due to easy recoverable, high catalytic activity and the cogeneration of different reactive species. (C) 2017 Elsevier B.V. All rights reserved.
机译:非均相光催化剂,TiO 2官能化磁性活性炭(T @ MPAC)作为新的过氧键硫酸盐(PMS)活化剂,用于改善水性介质中苯并三唑(BTA)的氧化降解。为了表征合成催化剂的特征,施加了合成催化剂的特征,施加了XRD,FESEM,EDS,BET,TEM,PL和UV-VIS DRS技术。在批量环境中研究了操作参数的影响即溶液pH,反应时间和催化剂剂量,PMS和BTA。提出了一种可粘合的氧化机理和BTA降解的反应途径。进行潜在的催化,可回收性,耐久性和猝灭研究。在激活不同氧化剂中的T @ MPAc的催化活性也评价。在优化条件下,在第五次循环之后,发现BTA的降解和矿化率分别为71.6和38.7%。通过PMS>过硫酸盐>臭氧> H 2 O 2的顺序提高了BTA降解对BTA降解的T @ MPAc的催化活性。诱捕实验证实了中心点OH,SO4中心点,O-2中心点自由基作为系统的反应性物种的参与。在T @ MPAC / PMS / UV系统中包含的反应性物种(即中心点OH,SO4中心点,O-2中心点和孔)中,SO4中心点在控制氧化反应方面具有显着作用。在清除剂存在下降低降解速率是IPA> BQ> T-BuOH> Ki。催化性能在氯离子存在下掉落,而磷酸盐,硝酸盐和硫酸根阴离子的影响较小。催化剂在连续五种用途后显示出良好的再循环性和稳定性。为了得出结论,由于易于可回收,高催化活性和不同反应性物种的热量,可以成功地应用于T @ MPAC / UV和PMS的偶联作为一种新颖的和有效的技术,以降解废水中的有机物质。 (c)2017 Elsevier B.v.保留所有权利。

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