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Characterization of Zirconium Sulfate Supported on Zirconia and Activity for Acid Catalysis

机译:氧化锆负载硫酸锆的表征及酸催化活性

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Zirconium sulfate supported on zirconia catalysts were prepared by impregnation of powdered Zr(OH)4 with zirconium sulfate aqueous solution followed by calcining in air at high temperature. The characterization of prepared catalysts was performed using Fourier transform infrared (FTIR), X-ray diffraction (XRD), differential scanning calorimetry (DSC), and by the measurement of surface area. The addition of zirconium sulfate to zirconia increased the phase transition temperature of ZrO2 from amorphous to tetragonal due to the interaction between zirconium sulfate and zirconia, and the specific surface area and acidity of catalysts increased in proportion to the zirconium sulfate content up to 10 wt% of Zr(SO4)2. Infrared spectra of ammonia adsorbed on Zr(SO4)2/ZrO2 showed the presence of Bronsted and Lewis acid sites on the surface. 10-Zr(SO4)2/ZrO2 calcined at 600∩ exhibited maximum catalytic activities for 2-propanol dehydration and cumene dealkylation. The catalytic activities for both reactions were correlated with the acidity of catalysts measured by ammonia chemisorption method.
机译:通过用硫酸锆水溶液浸渍粉末状的Zr(OH) 4 ,然后在空气中高温煅烧来制备负载在氧化锆催化剂上的硫酸锆。使用傅里叶变换红外(FTIR),X射线衍射(XRD),差示扫描量热法(DSC)并通过测量表面积来进行制备催化剂的表征。由于硫酸锆和氧化锆之间的相互作用,向氧化锆中添加硫酸锆使ZrO 2 的相变温度从非晶态转变为四方晶,并且催化剂的比表面积和酸度与碳纳米管成比例地增加。硫酸锆含量最高可达Zr(SO 4 2 的10 wt%。吸附在Zr(SO 4 2 / ZrO 2 上的氨的红外光谱表明表面存在布朗斯台德和路易斯酸位。 600℃煅烧的10-Zr(SO 4 2 / ZrO 2 对2-丙醇脱水和枯烯脱烷基反应具有最大的催化活性。两种反应的催化活性均与通过氨化学吸附法测得的催化剂的酸度相关。

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