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稀土改性Ni/γ-Al_2O_3催化剂上甲烷化反应积碳的初步研究 总被引:1,自引:0,他引:1
本文系统考察了镧系14种稀土氧化物对镍基甲烷化催化剂积碳的影响,发现大多数稀土的添加使催化剂活性提高,寿命延长,尤以Dy,Pr,Sm效果最佳,主要作用是稀土添加剂促进了甲烷化活性中心数的增长,有抑止积碳的能力,缩短催化剂的增活期。 相似文献
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稀土对Ru基加氢催化剂的改性研究 总被引:1,自引:1,他引:0
采用浸渍法制备了一系列的Ru-RE/sepiolite(海泡石)(RE=La,Ce,Tb或Y)催化剂,以二氧化碳甲烷化及苯加氢为探针反应,以TPD、TPSR、CO化学吸附和CS2中毒为手段系统地研究了RE对Ru/sepiolite催化剂的改性机制。结果表明,RE的加入显著影响Ru/sepiolite催化剂的催化性能。从机理上看,RE对CO2甲烷化性能的影响是通过对反应物活化过程中的能量因素及几何因素的调节作用来实现的。RE的加入增加了Ru/sepiolite催化剂的活性表面积、活性中心数和催化剂抗毒物的能力。研究还表明,RE的添加顺序亦对Ru/sepiolite催化剂的活性构成一定的影响。 相似文献
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A series of Ni-Sm/sepiolite catalysts were prepared by impregnation. The modification of Sm2O3 for Ni/sepiolite was investigated by TPR, XPS and poisoning of CS2, respectively. The results indicate that the addition of Sm2O3 improves the activity of hydrogenation and anti-poisoning ability of Ni/sepiolite catalyst, and it also increases the dispersion of nickel atoms over support and the amount of active nickel atoms in catalyst. Effect of Sm203 on Ni/sepiolite catalyst ineludes not only electronic effect but also steric effect, whereas electronic effect seems to be principal. 相似文献
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考察了煅后焦中微量元素镍对炭阳极反应活性的影响,并对炭阳极的二氧化碳反应性、空气反应性进行了测试。结果表明,适量的镍元素可以改善炭阳极在CO2中的残极率、粉化率和质量损失率;也能提高炭阳极在空气中的残极率、粉化率和质量损失率。镍元素的添加对炭阳极的CO2反应性和空气反应性均有抑制作用,可改善炭阳极质量,降低炭阳极的额外消耗。 相似文献
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In the early 1980s, it was reported thatrare earth oxide can improve the properties ofnickel catalysts['J. In this paper, the effect ofLaZO3 on activity of methanation of CO andCOb over Ni-Mo/Y-A12O3 was studied. The relationship between catalytic activity, surfacebehaviour and the role of LaZO3 in Mi-Mo-La/Y-Allot catalyst were investigated by means oftransmission electron microscope (TEM ), Xray photoelectron spectroscopy (XPS ), andchemisorption of CO.1 Experimental1. I Prepara… 相似文献
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TheresearchontheroastreactionofBaotouconcentrateofrareearthwithNa2CO3additionsbeganin1963andtheindustrialscaleexperiments... 相似文献
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采用Ca(OH)2为化学活化剂,对颗粒活性炭进行改性。结果表明,在Ca(OH)2用量为100mL、改性温度80℃、改性时间2h、干燥时间6h时,改性后的活性炭吸附容量达到最大,为3.91mmol/g。 相似文献
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稀土掺杂锂离子电池正极材料LiCoO2的影响研究 总被引:10,自引:0,他引:10
在合成LiCoO2的基础上,采用共沉淀法掺杂稀土La、Ce、Lu、Y等合成制备了LiRExCo1-xo2,并对其进行了XRD、SEM表征及电性能测试.结果表明,合成的LiRE、Co1-xO2具有LiCoO2结构,当稀土La的加入量x<0.05时,稀土能完全形成单一LiRExCo1-xO2相;稀土的掺入能促进LiCoO2结晶,同时使104面的相对衍射强度增加;LiRExCo1-xO2首次放电容量达147.4 mA·h/g,循环稳定性有所提高. 相似文献
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A series of CuO-ZnO-Al2O3-La2O3 /HZSM-5 bifunctional catalysts with various La loadings for dimethyl ether (DME) directly synthesized from CO2 hydrogenation were prepared. The catalysts were characterized with N2 adsorption-desorption, X-ray diffraction (XRD), H2 temperature-programmed reduction (H2-TPR), NH3 temperature-programmed desorption (NH3-TPD) and N2O titration techniques, and tested for the synthesis of DME directly from CO2 hydrogenation in a fixed-bed reactor. The results showed that the reducibility, dispersion of bifunctional catalysts were strongly dependent on the addition of La. With the addition of appropriate amount of La, the crystallite size of CuO was decreased and the dispersion of Cu on the surface was enhanced, which resulted in the increased conversion of CO2 . It was also found that the selectivity to DME was related to the intensity and amount of strong acid site on the catalyst surface. The presence of La favored the production of DME, and the optimum catalytic activity was obtained when the amount of La was 2.0 wt.%. 相似文献
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The CuO/CeO2 catalysts were investigated by means of X-ray diffraction(XRD),laser Raman spectroscopy(LRS),X-ray photoelectronic spectroscopy(XPS),temperature-programmed reduction(TPR),in situ Fourier transform infrared spectroscopy(FTIR) and NO+CO reaction.The results revealed that the low temperature(150 °C) catalytic performances were enhanced for CO pretreated samples.During CO pretreatment,the surface Cu+/Cu0 and oxygen vacancies on ceria surface were present.The low valence copper species activated the adsorbed CO and surface oxygen vacancies facilitated the NO dissociation.These effects in turn led to higher activities of CuO/CeO2 for NO reduction.The current study provided helpful understandings of active sites and reaction mechanism in NO+CO reaction. 相似文献
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