采用溶胶-凝胶法制备了系列生物质改性复合纳米TiO_2。以亚甲基蓝溶液为模拟污染物,考察了其可见光催化活性,并确定了最佳制备工艺。通过X射线光电子能谱(XPS)、X射线衍射(XRD)、场发射扫描电镜(FESEM)、紫外-可见漫反射光谱(UV-Vis-DRS)、荧光光谱(PL)等手段对催化剂样品进行了表征。实验结果表明,催化剂对亚甲基蓝的光催化降解适应一级反应动力学,复合TiO_2和纯TiO_2的反应速率常数分别为0.4990 h-1和0.0305h-1,且复合催化剂实现了C、N、S、P、K等多元素的共掺杂。相比纯TiO_2,复合TiO_2的比表面积增大,结晶度升高,光生载流子复合率降低,吸收边带红移,禁带宽度窄化了0.09 e V。
采用溶胶-超声空化技术同步合成了生物质多元自掺杂TiO_2复合催化剂,通过场发射扫描电镜(FESEM)、X射线衍射(XRD)、X射线光电子能谱(XPS)、紫外-可见漫反射光谱(UV-vis)、傅里叶变换红外光谱(FT-IR)、光致发光光谱(PL)等对样品进行了表征分析。结果表明,复合催化剂实现了C、N、P、Cl、K等元素的同步掺杂,合成了多元共掺杂复合TiO_2;相比纯TiO_2,复合催化剂的禁带宽度窄化了0.21 e V,表面羟基与活性位点增多,光生载流子复合几率降低,结晶度提高,比表面积增大。以亚甲基蓝(MB)为目标污染物,研究了复合催化剂的可见光光催化性能。实验结果表明,在可见光照射下,光催化反应2 h时,复合催化剂对亚甲基蓝的降解效率最高可达98%。
Using glucose and sucrose as the electron donors,the photocatalytic hydrogen evolution over Pt/TiO2 was investigated.Glucose and sucrose enhance notably the activity for hydrogen generation.The amounts of produced H2 increase almost proportionally to time within 5 h irradiation in the reaction systems of the two electron donors.The effect of the initial concentration of glucose and sucrose on the reaction rate is consistent with the Langmuir-Hinshelwood kinetic model.After 5 h irradiation,the COD（chemical oxygen demand） in the reaction system of glucose and in that of sucrose decrease by 33.2%,11.4% respectively.The effect of electron donors on the flat-band potential of conduction band of TiO2 electrode was investigated.The flat-band potential of conduction band of TiO2 electrode in the presence of the electron donors shifts negatively,and the shift in the presence of glucose is larger than that in the presence of sucrose due to glucose having a larger adsorption amount on TiO2.
