The g-C_(3)N_(4)/BiOI/CdS double Z-scheme heterojunction photocatalyst with I_(3)^(-)/I^(-) redox pairs is prepared using simple calcination,solvothermal,and solution chemical deposition methods.The photocatalyst comp...The g-C_(3)N_(4)/BiOI/CdS double Z-scheme heterojunction photocatalyst with I_(3)^(-)/I^(-) redox pairs is prepared using simple calcination,solvothermal,and solution chemical deposition methods.The photocatalyst comprised mesoporous,thin g-C_(3)N_(4) nanosheets loaded on flower-like microspheres of BiOI with CdS quantum dots.The g-C_(3)N_(4)/BiOI/CdS double Z-scheme heterojunction has abundant active sites and in situ redox I_(3)^(-)/I^(-) mediators and shows quantum size effects,which are all conducive to enhancing the separation of photoinduced charges and increasing the photocatalytic degradation efficiency for bisphenol A,a model pollutant.Specifically,the heterojunction photocatalyst achieves a photocatalytic degradation efficiency for bisphenol A of 98.62%in 120 min and photocatalytic hydrogen production of 863.44 mmol h^(-1) g^(-1) on exposure to visible light.The excellent visible-light photocatalytic performance is as a result of the Z-scheme heterojunction,which extends absorption to the visible light region,as well as the I_(3)^(-)/I^(-) pairs,which accelerate photoinduced charge carrier transfer and separation,thus dramatically boosting the photocatalytic performance.In addition,the key role of the charge transfer across the indirect Z-scheme heterojunction has been elucidated and the transfer mechanism is confirmed based on the detection of intermediate I_(3)^(-)ions.Thus,this study provides guidelines for the design of indirect Z-scheme heterojunction photocatalysts.展开更多
从芝麻中提取总RNA,用反转录聚合酶链式反应得到芝麻蛋白Ses i 3基因,构建pET-22b(+)质粒表达载体,转入BL21(DE3)感受态细胞宿主表达菌中诱导表达,经镍离子亲和层析柱获得纯品目的蛋白。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳结果显示目的...从芝麻中提取总RNA,用反转录聚合酶链式反应得到芝麻蛋白Ses i 3基因,构建pET-22b(+)质粒表达载体,转入BL21(DE3)感受态细胞宿主表达菌中诱导表达,经镍离子亲和层析柱获得纯品目的蛋白。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳结果显示目的蛋白分子质量约为66 kDa。进而采用BALB/c小鼠过敏模型评价重组Ses i 3蛋白与天然Ses i 3蛋白诱发小鼠芝麻过敏反应的差别,通过测定相关过敏性指标(特异性抗体羊抗鼠免疫球蛋白(immunoglobulin,Ig)E、IgG1和IgG2a;细胞因子白细胞介素(interleukin,IL)-4、IL-5、干扰素-γ和组胺)发现,重组蛋白Ses i 3诱发小鼠芝麻过敏的能力与天然Ses i 3蛋白相似。因此,本研究通过原核表达系统获得重组的芝麻重组蛋白Ses i 3,并证实其与天然Ses i 3蛋白具有相似的免疫活性,可以用于后续的芝麻致敏性研究。展开更多
基金support of this work by the National Natural Science Foundation of China(51869006)Jiangxi Natural Science Foundation of China(20171BAB216050)Water Science and Technology Fund of Jiangxi Province in China(KT201702).
文摘The g-C_(3)N_(4)/BiOI/CdS double Z-scheme heterojunction photocatalyst with I_(3)^(-)/I^(-) redox pairs is prepared using simple calcination,solvothermal,and solution chemical deposition methods.The photocatalyst comprised mesoporous,thin g-C_(3)N_(4) nanosheets loaded on flower-like microspheres of BiOI with CdS quantum dots.The g-C_(3)N_(4)/BiOI/CdS double Z-scheme heterojunction has abundant active sites and in situ redox I_(3)^(-)/I^(-) mediators and shows quantum size effects,which are all conducive to enhancing the separation of photoinduced charges and increasing the photocatalytic degradation efficiency for bisphenol A,a model pollutant.Specifically,the heterojunction photocatalyst achieves a photocatalytic degradation efficiency for bisphenol A of 98.62%in 120 min and photocatalytic hydrogen production of 863.44 mmol h^(-1) g^(-1) on exposure to visible light.The excellent visible-light photocatalytic performance is as a result of the Z-scheme heterojunction,which extends absorption to the visible light region,as well as the I_(3)^(-)/I^(-) pairs,which accelerate photoinduced charge carrier transfer and separation,thus dramatically boosting the photocatalytic performance.In addition,the key role of the charge transfer across the indirect Z-scheme heterojunction has been elucidated and the transfer mechanism is confirmed based on the detection of intermediate I_(3)^(-)ions.Thus,this study provides guidelines for the design of indirect Z-scheme heterojunction photocatalysts.
文摘从芝麻中提取总RNA,用反转录聚合酶链式反应得到芝麻蛋白Ses i 3基因,构建pET-22b(+)质粒表达载体,转入BL21(DE3)感受态细胞宿主表达菌中诱导表达,经镍离子亲和层析柱获得纯品目的蛋白。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳结果显示目的蛋白分子质量约为66 kDa。进而采用BALB/c小鼠过敏模型评价重组Ses i 3蛋白与天然Ses i 3蛋白诱发小鼠芝麻过敏反应的差别,通过测定相关过敏性指标(特异性抗体羊抗鼠免疫球蛋白(immunoglobulin,Ig)E、IgG1和IgG2a;细胞因子白细胞介素(interleukin,IL)-4、IL-5、干扰素-γ和组胺)发现,重组蛋白Ses i 3诱发小鼠芝麻过敏的能力与天然Ses i 3蛋白相似。因此,本研究通过原核表达系统获得重组的芝麻重组蛋白Ses i 3,并证实其与天然Ses i 3蛋白具有相似的免疫活性,可以用于后续的芝麻致敏性研究。
