用溶胶-凝胶法制得Cu/Fe2O3-TiO2光催化材料。用XRD、Ram an、TPR、IR、TEM、UV-V is DRS测试技术和光催化反应等对固体材料的结构和性能进行了表征。结果表明,Fe2O3的质量分数为10%时,在TiO2表面以单分子层分散,Fe2O3的引入使TiO2吸光...用溶胶-凝胶法制得Cu/Fe2O3-TiO2光催化材料。用XRD、Ram an、TPR、IR、TEM、UV-V is DRS测试技术和光催化反应等对固体材料的结构和性能进行了表征。结果表明,Fe2O3的质量分数为10%时,在TiO2表面以单分子层分散,Fe2O3的引入使TiO2吸光限蓝移。Fe2O3含量超过单分子层分散时,有晶相Fe2O3生成,光吸收性能下降。Fe—O—Ti键的形成加强了半导体之间的相互作用,有利于光生载流子在半导体间的输送。少量Cu的引入,使复合材料的吸光域向可见光范围扩展。光催化反应性能与材料的光响应能力密切相关。在光催化CO2和CH3NH2直接合成NH2CH2COOH的反应中,负载质量分数为10%Fe2O3的光催化反应性能最优。在120℃、常压、空速200 h-1、CO2与CH3NH2摩尔比为1∶1和6.5×10-4W/cm2的紫外灯照射下,CH3NH2转化率为1.35%,NH2CH2COOH选择性达92.0%。展开更多
The lime-Cu^(2+)-xanthate process is commonly used for the flotation separation of sphalerite from pyrite.In this process,lime is added to the pulp to inhibit the floatability of pyrite.However,the excessive use of li...The lime-Cu^(2+)-xanthate process is commonly used for the flotation separation of sphalerite from pyrite.In this process,lime is added to the pulp to inhibit the floatability of pyrite.However,the excessive use of lime can result in pipeline blockage and inadequate recovery of associated precious metals.Therefore,it is necessary to develop new flotation process that minimizes or eliminates the use of lime.In this paper,a novel Fe^(3+)-Cu^(2+)-butyl xanthate process was developed as an alternative to lime for separating of sphalerite from pyrite.The flotation results indicated that with the artificially-mixed minerals,the flotation recovery of pyrite was lower than 16%and that of sphalerite was higher than 47%at pH 5.0−10.0.The zeta potential measurements revealed that ferric ion preferred to adsorb on pyrite,and copper ion displaced with zinc ion from the lattice at the interface of sphalerite.The wettability analyses indicated that the hydrophobicity of sphalerite surface increased apparently after being treated with Fe^(3+)-Cu^(2+)-BX,while the hydrophobicity of pyrite surface remained nearly unchanged.With XPS analysis,Cu-S bond and hydrophilic ferric hydroxide were detected separately on the surface of sphalerite and pyrite after conditioning with Fe^(3+)-Cu^(2+)-BX,which facilitated the flotation separation of sphalerite from pyrite with butyl xanthate collector.展开更多
V2O5/WO3‐TiO2 and V2O5/WO3‐TiO2‐SiO2 catalysts were prepared by a wetness impregnation method, and both the catalysts were hydrothermally aged at 750℃ in 10 vol%H2O/air for 24 h. The catalysts were evaluated for N...V2O5/WO3‐TiO2 and V2O5/WO3‐TiO2‐SiO2 catalysts were prepared by a wetness impregnation method, and both the catalysts were hydrothermally aged at 750℃ in 10 vol%H2O/air for 24 h. The catalysts were evaluated for NOx conversion using NH3 as the reductant. Hydrothermal ageing decreased the NOx conversion of V2O5/WO3‐TiO2 catalyst severely over the entire measured tem‐perature range. Interestingly, the NH3‐SCR activity of the silica‐modified catalyst at 220–480℃ is enhanced after ageing. The catalysts were characterized by X‐ray diffraction, nitrogen adsorption, X‐ray fluorescence, Raman spectroscopy, H2 temperature‐programmed reduction, and NH3 temper‐ature‐programmed desorption. The addition of silica inhibited the phase transition from anatase to rutile titania, growth of TiO2 crystallite size and shrinkage of catalyst surface area. Consequently, the vanadia species remained highly dispersed and the hydrothermal stability of the V2O5/WO3‐TiO2 catalyst was significantly improved.展开更多
文摘用溶胶-凝胶法制得Cu/Fe2O3-TiO2光催化材料。用XRD、Ram an、TPR、IR、TEM、UV-V is DRS测试技术和光催化反应等对固体材料的结构和性能进行了表征。结果表明,Fe2O3的质量分数为10%时,在TiO2表面以单分子层分散,Fe2O3的引入使TiO2吸光限蓝移。Fe2O3含量超过单分子层分散时,有晶相Fe2O3生成,光吸收性能下降。Fe—O—Ti键的形成加强了半导体之间的相互作用,有利于光生载流子在半导体间的输送。少量Cu的引入,使复合材料的吸光域向可见光范围扩展。光催化反应性能与材料的光响应能力密切相关。在光催化CO2和CH3NH2直接合成NH2CH2COOH的反应中,负载质量分数为10%Fe2O3的光催化反应性能最优。在120℃、常压、空速200 h-1、CO2与CH3NH2摩尔比为1∶1和6.5×10-4W/cm2的紫外灯照射下,CH3NH2转化率为1.35%,NH2CH2COOH选择性达92.0%。
基金Project(52204363)supported by the National Natural Science Foundation of ChinaProject(2024JJ8042)supported by the Hunan Natural Science Foundation,ChinaProject(22C0220)supported by the Education Department of Hunan Province,China。
文摘The lime-Cu^(2+)-xanthate process is commonly used for the flotation separation of sphalerite from pyrite.In this process,lime is added to the pulp to inhibit the floatability of pyrite.However,the excessive use of lime can result in pipeline blockage and inadequate recovery of associated precious metals.Therefore,it is necessary to develop new flotation process that minimizes or eliminates the use of lime.In this paper,a novel Fe^(3+)-Cu^(2+)-butyl xanthate process was developed as an alternative to lime for separating of sphalerite from pyrite.The flotation results indicated that with the artificially-mixed minerals,the flotation recovery of pyrite was lower than 16%and that of sphalerite was higher than 47%at pH 5.0−10.0.The zeta potential measurements revealed that ferric ion preferred to adsorb on pyrite,and copper ion displaced with zinc ion from the lattice at the interface of sphalerite.The wettability analyses indicated that the hydrophobicity of sphalerite surface increased apparently after being treated with Fe^(3+)-Cu^(2+)-BX,while the hydrophobicity of pyrite surface remained nearly unchanged.With XPS analysis,Cu-S bond and hydrophilic ferric hydroxide were detected separately on the surface of sphalerite and pyrite after conditioning with Fe^(3+)-Cu^(2+)-BX,which facilitated the flotation separation of sphalerite from pyrite with butyl xanthate collector.
基金supported by the National Natural Science Foundation of China (51372137)the National High Technology Research and Development Program of China (863 Program,2015AA034603)~~
文摘V2O5/WO3‐TiO2 and V2O5/WO3‐TiO2‐SiO2 catalysts were prepared by a wetness impregnation method, and both the catalysts were hydrothermally aged at 750℃ in 10 vol%H2O/air for 24 h. The catalysts were evaluated for NOx conversion using NH3 as the reductant. Hydrothermal ageing decreased the NOx conversion of V2O5/WO3‐TiO2 catalyst severely over the entire measured tem‐perature range. Interestingly, the NH3‐SCR activity of the silica‐modified catalyst at 220–480℃ is enhanced after ageing. The catalysts were characterized by X‐ray diffraction, nitrogen adsorption, X‐ray fluorescence, Raman spectroscopy, H2 temperature‐programmed reduction, and NH3 temper‐ature‐programmed desorption. The addition of silica inhibited the phase transition from anatase to rutile titania, growth of TiO2 crystallite size and shrinkage of catalyst surface area. Consequently, the vanadia species remained highly dispersed and the hydrothermal stability of the V2O5/WO3‐TiO2 catalyst was significantly improved.
基金supported by the National Natural Science Foundation of China(20976162,21103149,20906079)Natural Science Foundation of Zhejiang Province,China(R5100266)Significant Science and Technology Project of Zhejiang Province,China(2010C13001)~~
