Center for Advanced Optoelectronic Functional Materials Research, Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024, People's Republic of China.
J Hazard Mater. 2012 Jul 30;225-226:155-63. doi: 10.1016/j.jhazmat.2012.05.006. Epub 2012 May 9.
In this paper, Bi(2)MoO(6) microtubes (BMO-MTs) were obtained by a two-step fabrication route. By using the electrospun polyacrylonitrile (PAN) microfibers as structure-directing hard template and through ethylene glycol solvothermal method, polyacrylonitrile/Bi(2)MoO(6) (PAN/BMO) hybrid microfibers with core-shell structures were prepared. Through heat treatment of the as-prepared PAN/BMO to remove the PAN core, Bi(2)MoO(6) with tubes-structured were obtained. The thickness of BMO-MTs was controlled by changing the Bi(2)MoO(6) loading percentage of PAN/BMO which could be obtained through ethylene glycol solvothermal process with precursor different concentration for the preparation of Bi(2)MoO(6). And, the crystal structure and morphology of BMO-MTs strongly depended on the calcination temperature when heat-treating the as-prepared PAN/BMO. Photocatalytic tests show that the BMO-MTs possess a much higher degradation rate of Rhodamine B (RB) than that of Bi(2)MoO(6) prepared by solid-state reaction and conventional P25. The improved photocatalytic performance could be ascribed to the hollow multi channelled structure and large surface area. The BMO-MTs could be reclaimed easily by sedimentation from the photocatalytic reaction solution due to the large length to diameter ratio of one-dimensional tubes structures. Moreover, such simple and versatile strategy can provide a general way to fabricate other tubes structures of Bi(III)-containing oxides, such as Bi(2)WO(6) and BiVO(4) microtubes.
本文采用两步法制备了 Bi(2)MoO(6) 微管(BMO-MTs)。以静电纺丝的聚丙烯腈(PAN)微纤维为结构导向硬模板,通过乙二醇溶剂热法制备了具有核壳结构的聚丙烯腈/ Bi(2)MoO(6)(PAN/BMO)杂化微纤维。通过对所制备的 PAN/BMO 的热处理去除 PAN 核,得到具有管状结构的 Bi(2)MoO(6)。通过改变 PAN/BMO 中 Bi(2)MoO(6) 的负载百分比,可以控制 BMO-MTs 的厚度,这可以通过不同浓度的前驱体制备乙二醇溶剂热过程来实现。并且,BMO-MTs 的晶体结构和形态强烈依赖于热处理前体 PAN/BMO 时的煅烧温度。光催化测试表明,BMO-MTs 具有比固相反应和常规 P25 制备的 Bi(2)MoO(6) 更高的 Rhodamine B(RB)降解率。改进的光催化性能可归因于中空多通道结构和大表面积。由于一维管状结构的长径比大,BMO-MTs 可以很容易地通过沉降从光催化反应溶液中回收。此外,这种简单且通用的策略可以为制备其他含 Bi(III)的氧化物,如 Bi(2)WO(6)和 BiVO(4)微管的管状结构提供一种通用方法。