检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:王攀[1] 曹婷婷[1] 方艳芬[1] 罗光富[1] 李瑞萍[1] 黄应平[1]
机构地区:[1]三峡大学三峡库区生态环境教育部工程研究中心,湖北宜昌443002
出 处:《影像科学与光化学》2011年第1期11-23,共13页Imaging Science and Photochemistry
基 金:国家自然科学基金(20877048);湖北省高校优秀中青年创新团队计划(T200703);湖北省自然科学基金创新群体项目(2009CDA020);三峡大学研究生创新基金(200962)
摘 要:采用镉硫共沉淀方法制备了Hg掺杂CdS(HgxCd1-xS)光催化剂,运用X射线衍射法(XRD)、X射线光电子能谱(XPS)、透射电镜(TEM)和紫外-可见吸收光谱对所制备的催化剂进行了表征;利用可见光催化降解罗丹明B(Rhodi-amine B,RhB)和2,4-二氯苯酚(2,4-dichlorophenol,2,4-DCP)为探针反应,对HgxCd1-xS可见光催化活性进行了研究,通过跟踪RhB降解过程中吸收光谱的变化和总有机碳(TOC),评价了HgxCd1-xS对有机物的氧化降解及深度矿化能力.结果表明:HgxCd1-xS催化剂为立方晶型,Hg的最佳掺杂量为5%,其禁带宽度约为2.15 eV,对RhB和2,4-DCP均有较好的降解效果,实验条件下30 min RhB褪色率为100%,RhB的30 h矿化率为45.5%,2,4-DCP的16 h降解率达55%.HgxCd1-xS可见光光催化降解RhB具有较高的稳定性,Hg的掺杂能有效降低CdS光腐蚀问题.通过ESR跟踪测定光催化反应过程中产生的自由基,表明降解过程涉及·OH机理.Mercury doped CdS nanoparticles was prepared by co-precipitation method.The doped CdS nanoparticles were characterized by X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS),transmission electron microscope(TEM) and UV-Vis spectrum.The photo-catalytic degradation of Rhodamine B(RhB) and 2,4-dichlorophenol(2,4-DCP) under visible light were used as probe reactions to evaluate photo-catalytic activities by tracing the UV-Vis spectrum and the total organic carbon(TOC) changes.The results indicated that the best mole rate of Hg was 5% of the total metal amounts with the cubic phase crystal,and the band gap of Hg0.05Cd0.95S was 2.15 eV.In 30 minutes,the decolouration of RhB was 100% and the mineralization ratio of RhB was 45.5% in 30 hours,the mineralization of 2,4-DCP was up to 55% in hours with a high stability,the dop of the Hg can efficiently inhibit the photo-corrosion of CdS.The mechanism of degradation were evaluated by electron spin resonance(ESR),the findings showed that the degradation process involved hydroxyl radical course.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:3.128.205.62