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利用微弧氧化方法在钛网表明制备了Ag~+修饰的钛网膜电极,采用SEM和EDS对钛网膜电极进行表征,研究了钛网膜电极制备条件对三维光电催化亚甲基蓝脱色效率的影响。结果表明:当以微弧氧化电解液选择Na_3PO_4,Na_3PO_4的浓度6 g/L,电压270~310 V,电解液中加入的Ag~+的浓度为0.010 mol/L,微弧氧化5 min制备的钛网膜为主电极,三维光电催化体系中亚甲基蓝的浓度为5 mg/L,硫酸钠浓度为0.01 mol/L,外电压为2V,对亚甲基蓝的脱色率可以达到54.3%。 相似文献
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以蛭石作为载体,采用溶胶—凝胶法制备 TiO2/蛭石,TiO2/蛭石与石墨组成粒子电极,以溶胶凝胶法制备的钛网光电极为主电极,石墨片为阴极,亚甲基蓝溶液为目标降解物,支持电解质为无水硫酸钠溶液,固定光源为20 W 紫外灯,在恒定外电压的作用下,研究三维光电催化体系对亚甲基蓝溶液光电催化降解的效率。实验结果表明:当二氧化钛光电极的煅烧温度为550℃,TiO2/蛭石粒子的煅烧温度500℃,石墨0.8 g, TiO2/蛭石0.2 g,外接电压2 V,电极距离3 cm,无水硫酸钠溶液浓度0.02 mol/L,亚甲基蓝溶液浓度5 mg/L 时,三维光电催化实验对亚甲基蓝的脱色率达到51.9%。 相似文献
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采用溶胶-凝胶法制备沸石负载TiO2(TiO2/沸石)。将TiO2/沸石与活性炭按照不同比例混合为粒子电极,采用钛网作为主电极,硫酸钠溶液为助电解质,紫外灯为光源建立了三维电极光电催化体系,处理亚甲基蓝模拟废水。实验表明:当电极间距为4.0 cm、TiO2/沸石∶活性炭=2∶3、亚甲基蓝的初始浓度为3 mg/L,灯距为10 cm、电压为2.0 V、电解质浓度为0.04 mol/L、初始p H=6.0,光催化降解效率可达49.5%。三维电极光电催化效果优于二维电极光电催化与光催化效果。Fe3+离子掺杂提高了体系的光电催化效率,最大光电催化效率可达53.3%。 相似文献
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采用溶胶-凝胶-浸渍法在钛基底上制备了TiO2薄膜,以该薄膜为工作电极,石墨作对电极,饱和甘汞电极为参比电极,建立光电催化反应体系,对亚甲基蓝溶液进行了光电催化降解研究。结果表明:当外加偏压1.0 V,热处理温度500℃时,pH为10.2,TiO2薄膜光电催化活性最好,光电催化亚甲基蓝120 min可使其脱色率达64.... 相似文献
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采用高温热氧化法制备了Ti/SnO_2-Sb电极,用扫描电子显微镜(SEM)表征了电极的形貌。以Ti/SnO_2-Sb电极为阳极,钛网为阴极,对亚甲基蓝废水进行电催化氧化降解,研究不同因素对亚甲基蓝脱色率的影响,并分析了亚甲基蓝的降解效果。结果表明,当亚甲基蓝的初始浓度为100mg·L~(-1),电流密度为10mA·cm~(-2),电解质浓度为0.10mol·L~(-1),pH=10时,反应30min,亚甲基蓝的脱色率为98.8%,60min时溶液的COD去除率为72.8%。 相似文献
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以磷酸钠为电解液,采用微弧氧化技术制备钛基TiO2膜,以该膜为阳极,钛片为阴极与40 W紫外灯和稳压电源组成电助光催化体系,以大红染料模拟废水来评价TiO2膜光电催化能力。研究了酸度和亚铁离子质量浓度等因素对光催化的影响。结果表明:光电催化提高了TiO2膜阳极的降解率;阴极槽内亚铁离子存在会形成电-芬顿体系,有助于提高光电催化降解率。当电解液中支持电解质硫酸钠浓度为0.5 mol/L、pH=3时阳极槽的降解率达到38%,阴极槽亚铁离子质量浓度为3.0mg/L时降解率达到68%。 相似文献
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采用电化学阳极氧化法,在HF—H2O,NH4F—H2O,NH4F—H2O-乙二醇三种不同的电解液体系中,于Ti基底上制备了TiO2纳米管阵列薄膜,并在空气气氛中于500℃进行结晶热处理。以亚甲基蓝为模拟污染物,考察了TiO2纳米管阵列薄膜的光电催化降解效果,并比较了电解催化、光催化和光电催化对亚甲基蓝溶液降解效率的差异。结果表明在NH4F—H2O-乙二醇电解液体系中制备的TiO2纳米管阵列光电催化性能最好。经过340min后,催化效率达到了94.23%。 相似文献
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随着新型信息记录与数码影像技术的快速发展,以及环保型高能动力装置应用的需要,各种高技术领域均迫切需要更高性能的锂离子二次电池。其关键技术是锂离子电池材料,如正极活性物质、负极活性物质等的制造与应用。对此,近年来在国际上已形成新的研发热潮。本文介绍一些研发团队的科研成果,以利于对其引进、消化吸收、再创新。 相似文献
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The low-frequency dielectric characteristics of soda-lime and sodium-silicate glasses were determined as a function of temperature, electrode materials, surface condition, and specimen thickness. The resulting large dielectric constant (often called electrode polarization) was dependent on surface condition of the glass specimen when evaporated metal electrodes were used and insensitive to surface condition when paste electrodes were used. The space charge mechanism was suggested as an explanation for these phenomena. The dependence of the dielectric constant on frequency and specimen thickness agrees with predictions of theory 相似文献
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《Drying Technology》2013,31(4):821-836
Abstract The enhancement of drying rate by corona discharge from multiple wire electrodes has been experimentally evaluated in this study. The corona wind produced by an array of three wire electrodes, which resembles a series of slot jets, impinges, and removes moisture from the surface of 6 mm glass beads saturated with water. Corona discharges with positive and negative polarities have been considered. Two sets of experiments have been conducted (one with the cross-flow of air and the other without), at 1 kV increment from the corona threshold voltage to a maximum voltage of 25 kV. To evaluate the drying enhancement, a companion experiment was carried out simultaneously for each case under the same ambient conditions but without the application of electric field. Each experiment lasted for at least 5 h. The weight loss of water as well as the ambient temperature and humidity were measured. The results are compared with those obtained with a single wire electrode to evaluate the effectiveness of a multiple-wire system. 相似文献
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