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作 者:徐敏虹[1] 潘国祥[1] 陈海锋[1] 王坤燕[1] 童艳花[1]
机构地区:[1]湖州师范学院材料化学系,浙江湖州313000
出 处:《矿物学报》2016年第2期208-214,共7页Acta Mineralogica Sinica
基 金:浙江省自然科学基金(编号:LQ14B040003);湖州市科技计划项目(编号:2013GY05);湖州师范学院校级科研项目成果(编号:2015XJLK29)
摘 要:通过共沉淀法将水溶性四羧基镍酞菁(Ni Pc)负载到镍-铝碳酸根水滑石(Ni Al-LDHs)上,制备负载型催化剂(Ni Pc/Ni Al-LDHs)。采用XRD、FT-IR、UV-Vis、TG-DTA和SEM等技术对酞菁衍生物和Ni Pc/Ni Al-LDHs的结构进行表征。结果表明Ni Pc没有改变Ni Al-LDHs的晶型结构和热稳定性能。在10 mg/L、25 m L的甲基橙溶液、p H值为3、H2O2用量50μL的条件下,Ni Pc/Ni Al-LDHs协同H2O2光催化氧化降解甲基橙3 h后,甲基橙剩余率为16.33%。溶液p H值在3~7范围内,Ni Pc/Ni Al-LDHs/H2O2都能有效光催化氧化降解甲基橙,且光催化氧化降解过程涉及到羟基自由基反应。Based on Ni/Al hydrotalcite(Ni Al-LDHs), catalyst Ni Pc/Ni Al-LDHs loaded aqueous nickel tetracarboxylphthalocyanine(Ni Pc) was synthesized using a coprecipitation method. Structures, morphologies and thermal properties of the phthalocyanine derivatives and catalyst were characterized by XRD, FT-IR, UV-Vis, TG-DTA and SEM. Results show that although the Ni Pc is introduced on Ni Al-LDHs, the crystal structure and thermal stability of Ni Al-LDHs are unchanged. Photocatalytic oxidation degradation of methyl orange(MO) in the Ni Pc/Ni Al-LDHs/H2O2 system lasted for 3 hours. The residual rate of MO was 16.33 % under the the conditions of MO being 10 mg/L 25 m L, p H value of 3, and dosage of H2O2 being 50 μL. The Ni Pc/Ni Al-LDHs/H2O2 system has good photocatalytic oxidation activity for removing MO when the p H value of MO solution is in the range of 3-7. Furthermore, the process of photocatalytic oxidation degradation of MO involves an hydroxyl radical reaction.
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