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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Rate Enhancement and Rate Inhibition of Phenol Degradation over Irradiated Anatase and Rutile TiO2 on the Addition of NaF:New Insight into the Mechanism
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Rate Enhancement and Rate Inhibition of Phenol Degradation over Irradiated Anatase and Rutile TiO2 on the Addition of NaF:New Insight into the Mechanism

机译:辐照锐钛矿和金红石型TiO2对NaF的苯酚降解的速率增强和速率抑制:机理的新见解

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Several studies have shown that addition of NaF into the aqueous dispersion of TiO2(Degussa P25)can result in significant enhancement in the photocatalytic degradation(PCD)of organic pollutants,ascribed to the enhanced production of free OH radicals in solution as a result of fluoride displacement of surface hydroxyl groups.In this work,we have observed different results of NaF addition for the PCD of phenol over synthetic TiO2 in aqueous suspension under UV light irradiation(lambda >= 320 nm).Upon the addition of NaF,the rate of phenol PCD was only increased with anatase,but it was decreased with rutile under similar conditions.In the presence of AgNO3,however,the fluoride-induced rate enhancement of phenol PCD could be observed with both anatase and rutile,ascribed to the increased rate of scavenging the conduction band electrons.As the catalyst sintering temperature was increased,the amount of fluoride adsorption on TiO2 was decreased,but the degree of PCD rate enhancement due to NaF addition as observed with anatase was first increased and then decreased,the trend of which was similar to that in the absence of NaF.The result reveals that the excess fluoride ions present in the suspension play some positive role to the phenol PCD,which is hardly interpreted by previous mechanism of surface fluorination.Moreover,as initial concentration of fluoride and initial pH of suspension were increased,the degree of rate enhancement was increased and decreased,respectively,which also could not be ascribed solely to the change in fluoride adsorption.Possible interference from catechol and hydroquinone intermediates and the fluoride-induced enhancement in the production of OH radicals in solution are analyzed.A new mechanistic model is proposed,involving enhanced desorption of surface bound OH radicals from irradiated TiO2,by fluoride ions present in the Helmholtz layers,through a fluorine hydrogen bond.
机译:几项研究表明,向TiO2(Degussa P25)的水分散体中添加NaF可以显着提高有机污染物的光催化降解(PCD),这归因于氟化物导致溶液中游离OH自由基的产生增加在这项工作中,我们观察到在紫外光(λ> = 320 nm)的水悬浮液中苯酚的PCD高于合成TiO2的PCD的NaF添加量的不同结果。苯酚PCD仅在锐钛矿条件下升高,而在金红石条件下降低。在AgNO3存在下,锐钛矿和金红石都能观察到氟诱导的苯酚PCD速率升高,归因于锐钛矿速率升高。随着催化剂烧结温度的升高,氟化物在TiO2上的吸附量减少,但Na导致PCD速率提高。用锐钛矿观察到的F的添加先增加然后减少,其趋势类似于没有NaF时的趋势。结果表明,悬浮液中存在的过量氟离子对酚PCD起到了积极作用,这是此外,随着氟化物初始浓度和悬浮液初始pH值的增加,速率增加的程度分别增加和减少,这也不能仅仅归因于氟化物吸附的变化。分析了邻苯二酚和对苯二酚中间体可能产生的干扰以及氟化物诱导溶液中OH自由基生成的增强。提出了一种新的机理模型,涉及通过亥姆霍兹中存在的氟离子增强被辐照的TiO2表面结合的OH自由基的解吸。层通过氟氢键。

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