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首页> 外文期刊>Journal of Chemical Engineering of Japan >PREPARATION AND PHOTOCATALYTIC REACTIONS OF TITANIUM DIOXIDE ULTRAFINE PARTICLES IN REVERSE MICELLAR SYSTEMS
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PREPARATION AND PHOTOCATALYTIC REACTIONS OF TITANIUM DIOXIDE ULTRAFINE PARTICLES IN REVERSE MICELLAR SYSTEMS

机译:反向胶束体系中二氧化钛超细颗粒的制备及光催化反应

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摘要

Photocatalytic oxidation of cyclohexane forming the organic phase of reverse micellar systems on in situ prepared TiO2 ultrafine particles has been investigated. The cyclohexane was photo-oxidized on the TiO2 ultrafine particles to form cyclohexanone and cyclohexanol under air-saturated conditions. In the absence of O-2, H-2 was generated via reduction of water in the micellar waterpools. CO was also generated in the absence of O-2 probably via a photocatalytic side reaction of I-butanol which was added as a solvent of the precursor of TiO2 (titanium tetrabutoxide: TTB) to prepare the particles, 1-butoxyl groups of TTB or l-butanol formed via hydrolysis of TTB. The molar ratio of water to TTB, W-t (=[H2O]/[TTB]) was a major factor in controlling the photocatalytic reaction behavior of the system. When the irradiation was carried out under air-saturated conditions for 18 h, the consumption rate of O-2 increased monotonously as the value of the parameter W-t decreased, while the quantities of cyclohexanone and cyclohexanol formed decreased at W-t<10. This can be attributed to a side reaction of 1-butoxyl groups of TTB molecules which is oxidized more easily than cyclohexane. This reaction becomes prominent in the extremely low W-t range owing to incomplete hydrolysis of TTB molecules. [References: 25]
机译:研究了原位制备的TiO2超细颗粒对环己烷的光催化氧化反应形成胶束体系反胶相的有机相。在空气饱和条件下,将环己烷在TiO2超细颗粒上进行光氧化,形成环己酮和环己醇。在没有O-2的情况下,H-2是通过减少胶束水池中的水生成的。在不存在O-2的情况下也可能通过异丁醇的光催化副反应生成CO,该异丁醇是作为TiO2前体(四丁氧基钛:TTB)的溶剂加入而制备的,其颗粒为TTB的1-丁氧基或通过TTB的水解形成1-丁醇。水与TTB的摩尔比W-t(= [H2O] / [TTB])是控制系统光催化反应行为的主要因素。当在空气饱和条件下照射18 h时,随着参数W-t值的减小,O-2的消耗率单调增加,而在W-t <10时,环己酮和环己醇的形成量减少。这可以归因于TTB分子的1-丁氧基的副反应,该副反应比环己烷更容易被氧化。由于TTB分子的不完全水解,该反应在极低的W-t范围内变得显着。 [参考:25]

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