Hu Chechia, Chu Yi-Ching, Lin Yan-Ru, Yang Hung-Chun, Wang Ke-Hsuan
Department of Chemical Engineering, R&D Center for Membrane Technology and Research Center for Circular Economy, Chung Yuan Christian University, Chungli Dist., Taoyuan 32023, Taiwan.
Department of Industrial Chemistry, Tokyo University of Science, Shinjuku-ku, Tokyo 1620826, Japan.
Polymers (Basel). 2019 Jan 21;11(1):182. doi: 10.3390/polym11010182.
The development of visible-light-driven polymeric g-C₃N₄ is in response to an emerging demand for the photocatalytic dye degradation and reduction of hexavalent chromium ions. We report the synthesis of g-C₃N₄ from urea treated with various solvents such as methanol, ethanol, and ethylene glycol. The samples were characterized and the Williamson⁻Hall method was applied to investigate the lattice strain of the samples. The activity of the samples was evaluated by observing the degradation of methyl orange and K₂Cr₂O₇ solution under light irradiation. Photocatalytic reaction kinetics were determined as pseudo-first-order and zero-order for the degradation of methyl orange and reduction of hexavalent chromium, respectively. Due to the inhibited charge separation resulting from the small lattice strain, reduced crystal imperfection, and sheet-like structure, g-C₃N₄ obtained from ethanol-treated urea exhibited the highest activity among the evaluated samples.
可见光驱动的聚合氮化碳(g-C₃N₄)的发展是为了响应光催化降解染料以及还原六价铬离子这一新兴需求。我们报道了通过用甲醇、乙醇和乙二醇等各种溶剂处理尿素来合成g-C₃N₄。对样品进行了表征,并应用威廉姆森-霍尔(Williamson⁻Hall)方法研究样品的晶格应变。通过观察光照下甲基橙和K₂Cr₂O₇溶液的降解情况来评估样品的活性。光催化反应动力学对于甲基橙的降解和六价铬的还原分别确定为伪一级和零级。由于乙醇处理的尿素所得到的g-C₃N₄因晶格应变小、晶体缺陷减少以及片状结构而导致电荷分离受到抑制,在评估的样品中表现出最高的活性。