Laboratory of Catalysis Chemistry and Nanoscience, Department of Chemistry and Chemical Engineering, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China.
Nanoscale. 2012 Apr 7;4(7):2317-25. doi: 10.1039/c2nr12046a. Epub 2012 Feb 29.
Three-dimension ordered macroporous (3D-OM) bismuth vanadates with a monoclinic crystal structure and high surface area (18-24 m(2) g(-1)) have been prepared using ascorbic acid (AA)- or citric acid (CA)-assisted poly(methyl methacrylate) (PMMA)-templating strategy with bismuth nitrate and ammonium metavanadate as the metal sources, HNO(3) as the pH adjuster and ethylene glycol and methanol as the solvent. The materials were characterized by a number of analytical techniques. The photocatalytic performance of the porous BiVO(4) samples was evaluated for the degradation of phenol in the presence of a small amount of H(2)O(2) under visible light illumination. The effects of the initial phenol concentration and the H(2)O(2) amount on the photocatalytic activity of the photocatalyst were examined. It is shown that the chelating agent, AA or CA, and the amount in which it is added had a significant impact on the quality of the 3D-OM structure, with a "(Bi + V):chelating agent" molar ratio of 2:1 being the most appropriate. Among the as-prepared BiVO(4) samples, the one with a surface area of ca. 24 m(2) g(-1) showed the best visible light-driven photocatalytic performance for phenol degradation (phenol conversion = ca. 94% at phenol concentration = 0.1 mmol L(-1) and in the presence of 0.6 mL H(2)O(2)). A higher phenol conversion could be achieved within the same reaction time if the phenol concentration in the aqueous solution was lowered, but an excess amount of H(2)O(2) was not a favorable factor for the enhancement of the catalytic activity. It is concluded that the excellent photocatalytic activity of 3D-OM BiVO(4) is due to the high quality 3D-OM structured BiVO(4) that has a high surface area and surface oxygen vacancy density. We are sure that the 3D-OM material is a promising photocatalyst for the removal of organics from wastewater under visible light illumination.
采用抗坏血酸(AA)或柠檬酸(CA)辅助的聚甲基丙烯酸甲酯(PMMA)模板法,以五水硝酸铋和偏钒酸铵为金属源,以 HNO3 为 pH 调节剂,以乙二醇和甲醇为溶剂,制备了具有单斜晶体结构和高表面积(18-24 m2 g-1)的三维有序大孔(3D-OM)氧化铋钒。采用多种分析技术对材料进行了表征。在可见光照射下,以少量 H2O2 存在时,评价了多孔 BiVO4 样品对苯酚的光催化降解性能。考察了初始苯酚浓度和 H2O2 用量对光催化剂光催化活性的影响。结果表明,螯合剂 AA 或 CA 的种类及其添加量对 3D-OM 结构的质量有显著影响,(Bi+V):螯合剂摩尔比为 2:1 时最为适宜。在所制备的 BiVO4 样品中,比表面积约为 24 m2 g-1 的样品对苯酚降解具有最佳的可见光驱动光催化性能(在苯酚浓度为 0.1 mmol L-1 且存在 0.6 mL H2O2 时,苯酚转化率约为 94%)。如果降低水溶液中的苯酚浓度,可以在相同的反应时间内获得更高的苯酚转化率,但过量的 H2O2 不是提高催化活性的有利因素。结论是,3D-OM BiVO4 的优异光催化活性归因于具有高表面积和表面氧空位密度的高质量 3D-OM 结构 BiVO4。我们相信,3D-OM 材料是一种很有前途的可见光下去除废水中有机物的光催化剂。