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首页> 外文期刊>Journal of Hazardous Materials >Mechanism investigation on the enhanced photocatalytic oxidation of nonylphenol on hydrophobic TiO_2 nanotubes
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Mechanism investigation on the enhanced photocatalytic oxidation of nonylphenol on hydrophobic TiO_2 nanotubes

机译:疏水性TiO_2纳米管上壬基酚增强光催化氧化机理的研究

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摘要

Enhanced and selective photocatalytic oxidation of nonylphenol (NP), a typical hydrophobic endocrine disrupting chemicals (EDCs), was realized on hydrophobic titanium dioxide nanotubes (H-TiO2NTs), which was fabricated by an electrochemical anodization method, followed by grafting of perfluorooctyl groups. The water contact angle of catalyst surface changed from 21.1 degrees to 128.4 degrees after hydrophobic modification. H-TiO2NTs showed excellent photocatalytic oxidation performance for NP, that it was completely converted in 40 min under irradiation, which was improved for about 17% compared with the hydrophilic TiO2NTs. The enhanced photocatalytic performance of H-TiO2NTs was attributed to the stronger adsorption ability toward NP identified by ATR-FTIR, with an initial adsorption rate of 4 times as higher as that of bare TiO2NTs. Meanwhile, the hydrophobic surface of H-TiO2NTs was beneficial for generation of more hydroxyl radicals. The apparent rate constant of hydroxyl radicals' generation on H-TiO2NTs, which was the main oxidizing species, could reach 1.83 times that of the hydrophilic TiO2NTs. Both the two factors contributed to the successful competition of NP against the coexistent hydrophilic contaminates in the adsorption and oxidation on the catalyst surface, leading to the selective removal of NP in mixed systems finally.
机译:在疏水二氧化钛纳米管(H-TiO2NTs)上实现了壬基酚(NP)(一种典型的疏水性内分泌干扰化学物质(EDC))的增强和选择性光催化氧化,该二氧化钛纳米管通过电化学阳极氧化方法制备,然后接枝全氟辛基。疏水改性后,催化剂表面的水接触角从21.1度变为128.4度。 H-TiO2NTs对NP表现出优异的光催化氧化性能,在照射下40分钟即可完全转化,与亲水性TiO2NTs相比提高了约17%。 H-TiO2NTs的增强的光催化性能归因于ATR-FTIR鉴定的对NP的较强吸附能力,其初始吸附速率是裸TiO2NTs的4倍。同时,H-TiO2NTs的疏水表面有利于产生更多的羟基自由基。作为主要氧化物质的H-TiO2NTs上羟基自由基生成的表观速率常数可以达到亲水性TiO2NTs的1.83倍。这两个因素都促使NP成功地与催化剂表面吸附和氧化过程中共存的亲水性污染物竞争,最终导致混合体系中NP的选择性去除。

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