Sonochemical Research Center, Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, 91779 Mashhad, Iran.
Sonochemical Research Center, Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, 91779 Mashhad, Iran; Environmental Chemistry Research Center, Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, 91779 Mashhad, Iran.
J Colloid Interface Sci. 2016 Mar 15;466:227-37. doi: 10.1016/j.jcis.2015.12.034. Epub 2015 Dec 18.
In this study, a new method has developed for the synthesis of Ag/AgBr/Graphene-oxide (Ag/AgBr/GO) nanocomposite with high adsorption capacity and high photocatalytic activity in degradation of methyl orange (MO). In this method, ultrasound was applied in the synthesis and it was facilitated the process. The samples prepared under ultrasound were shown as Ag/AgBr/GO-U, and the samples under conventional method as Ag/AgBr/GO-C. The results of FT-IR, XRD, Raman, DRS and SEM confirmed the structure of the nanocomposites very well. Ultrasound played a key role in the formation of nanocomposite with smaller size of GO sheets and particles. Different amount of GO was used in the nanocomposite composition and their photocatalytic activities were compared. The MO in solution was completely degraded in 15 min, 30 min, and 45 min with Ag/AgBr/GO-U-1 that contained 1 mg mL(-1) GO, Ag/AgBr/GO-U-0.5 that contained 0.5 mg mL(-1) GO and Ag/AgBr/GO-C-0.5 that contained 0.5 mg mL(-1) GO, respectively. The chemical oxygen demand (COD) measurements displayed a complete mineralization in 30 min for Ag/AgBr/GO-U-0.5. The data obtained from the degradation experiments were fitted to the first-order kinetics and the adsorption obeyed the Langmuir model. The nanocatalyst did not exhibit significant loss of activity even after four cycles of successive uses. To determine the mechanism of photocatalytic degradation of MO, different scavengers were used. Based on the results, the superoxide radical, hydroxyl radical and hole had a key role in the degradation process. The Ag/AgBr/GO-U-1 nanocomposite exhibited the highest photocatalytic activity due to its high adsorption capacity and enhanced charge transfer.
在这项研究中,开发了一种新的方法,用于合成具有高吸附能力和高光催化活性的 Ag/AgBr/氧化石墨烯(Ag/AgBr/GO)纳米复合材料,用于降解甲基橙(MO)。在该方法中,超声应用于合成过程中,从而促进了该过程。在超声下制备的样品表示为 Ag/AgBr/GO-U,在常规方法下制备的样品表示为 Ag/AgBr/GO-C。FT-IR、XRD、拉曼、DRS 和 SEM 的结果很好地证实了纳米复合材料的结构。超声在形成具有较小 GO 片和颗粒尺寸的纳米复合材料方面发挥了关键作用。纳米复合材料组成中使用了不同量的 GO,并比较了它们的光催化活性。溶液中的 MO 在 15 分钟、30 分钟和 45 分钟内完全降解,分别用含有 1mg/mL(-1)GO 的 Ag/AgBr/GO-U-1、含有 0.5mg/mL(-1)GO 的 Ag/AgBr/GO-U-0.5 和含有 0.5mg/mL(-1)GO 的 Ag/AgBr/GO-C-0.5。化学需氧量(COD)测量显示,Ag/AgBr/GO-U-0.5 在 30 分钟内完全矿化。降解实验获得的数据拟合到一级动力学,吸附符合朗缪尔模型。纳米催化剂即使在连续使用四周期后也没有表现出明显的活性损失。为了确定 MO 光催化降解的机制,使用了不同的清除剂。根据结果,超氧自由基、羟基自由基和空穴在降解过程中起着关键作用。Ag/AgBr/GO-U-1 纳米复合材料由于具有高吸附能力和增强的电荷转移,表现出最高的光催化活性。