一种CeO2-CoOx复合氧化物载体及其制备方法

一种ＣｅＯ↓［２］－ＣｏＯ↓［ｘ］复合氧化物载体是Ｃｅ与Ｃｏ的摩尔比为Ｃｅ∶Ｃｏ＝０．１－０．６∶１，晶粒大小：１－５０ｎｍ，比表面积：５０－１８０ｍ↑［２］ｇ↑［－１］。采用利用溶胶凝胶法以钴和铈的无机盐溶液为前驱物，制备了ＣｅＯ↓［２］含量在低范围内的钴基复合氧化物。本发明具有制备的ＣｅＯ↓［２］－ＣｏＯ↓［ｘ］复合氧化物载体颗粒和组分分布均匀的优点。

一种CuO/Al2O3脱硫剂的再生方法

一种ＣｕＯ／Ａｌ＃－［２］Ｏ＃－［３］脱硫剂的再生方法是将吸硫的ＣｕＯ／γ－Ａｌ＃－［２］Ｏ＃－［３］脱硫剂在含氨气气氛中还原再生，再生温度为３５０－５００℃，空速为５００－３０００ｈ＃＋［－１］，再生时间为３０－９０分钟。本发明的再生过程简单，易操作，二次脱硫活性稳定，可实现脱硫温度下的有效还原再生；再生过程中生成的ＳＯ＃－［２］在低温条件下可与未反应的ＮＨ＃－［３］结合生成固体硫酸铵盐，不仅简化了再生后续处理工序，而且可增强本再生方法的经济效益，降低了脱硫综合成本。

一种CeO2-TiO2复合氧化物载体及其制备方法

一种ＣｅＯ↓［２］－ＴｉＯ↓［２］复合氧化物载体，其特征在于Ｃｅ∶Ｔｉ（摩尔比）为０．０５－０．４∶１，粒径为１－１００ｎｍ，比表面积为５０－２５０ｍ↑［２］·ｇ↑［－１］，孔体积为０．３－１．２ｃｍ↑［３］·ｇ↑［－１］，采用一般的混合沉淀、抽滤、洗涤、干燥、焙烧可制成不同比例的水凝胶、醇凝胶、气凝胶ＣｅＯ↓［２］－ＴｉＯ↓［２］复合氧化物载体，其特征在于采用钛的无机物为原料，所以大大降低了成本。

Preparation and characterization of nanocrystalline CeO2 by precipitation method

CeO2 nanocrystalline particulates with different sizes were prepared by precipitation method using ethanol as dispersive and protective reagent. XRD spectra show that the synthesized CeO2 has cubic crystalline structure of space group O-H(5)-F-M3M, when calcination temperature is in the range of 250 similar to 800 degreesC. TEM images reveal that CeO2 particles are spherical in shape. The average size of the particles increases with the increase of calcination temperature. Thermogravimetric analysis indicates that the weight loss of precursor mainly depends on the calcination temperature, and little depends on the calcination time. Measurements of CeO2 relative density show that the relative density of CeO2 nanocrystalline powders increases with increasing CeO2 particle size.

超细CeO2粉体的制备及其担载Pd催化剂的性能

中国科学院山西煤炭化学研究所

焙烧温度对CeO2改性Pd/Al2O3甲醇分解催化剂性能的影响

中国科学院山西煤炭化学研究所

Silicon dioxide coating of CeO2 nanoparticles by solid state reaction at room temperature

The synthesis Of SiO2 coated CeO2 nanoparticles by humid solid state reaction at room. temperature is described. Transmission electron microscope results show that CeO2 Particles were coated with a layer Of SiO2. Binding energy of Ce 3d(5/2) was shifted from 883.8 to 882.8 eV after coating in the XPS Ce 3d spectra. This confirms the chemical bond formation between SiO32- and Ce4+. Because the surface photovoltage property of CeO2 nanoparticles that were used as core materials in the experiment approaches to that of CeO2 macroparticles, peak P2 (electron transition from 0 2p on surface to Ce 4f) disappeared in the surface photovoltage spectrum of CeO2 nanoparticles. Also, the effect Of SiO2 on the electron transition from 0 2p to Ce 4f results in the lowering of surface photovoltage response intensity of P1 peak (electron transition from 0 2p in bulk to Ce 4f).