Kakeru Fujiwara, Shogo Kayano, M. Nishijima, Keisuke Kobayashi, T. Nanba, Taku Tsujimura
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引用次数: 1
摘要
采用火焰喷雾热解法制备了NiO和ceo2。NiO的比表面积和总孔容分别为251 m 2 g -1和2.3 cm 3 g -1, ceo2的比表面积和总孔容分别为338 m 2 g -1和3.3 cm 3 g -1。NiO的高孔隙率和高表面积使得一水乙酸铈浸渍可以沉积小的ceo2颗粒(~ 5 nm)。用5%的h2在500℃下还原1 H,将NiO转化为金属Ni。在还原过程中,ceo2阻碍了Ni颗粒的生长。因此,扫描透射电子显微镜观察到,尽管Ni含量极高(80 wt%),但Ni尺寸相对较小(~ 20 nm)。相比之下,使用四水合乙酸镍将Ni掺入ceo2载体后,h2还原后形成了不均匀的Ni颗粒(20-100 nm)。h2化学吸附测定表明,前一种催化剂的Ni颗粒表面积为13.7 m 2 g -1,是后一种催化剂的2.4倍。前一种催化剂在250℃时co2甲烷化率达到47%,是后一种催化剂的2倍。
Porous NiO Prepared by Flame Spray Pyrolysis for 80 wt% Ni–CeO 2 Catalyst and Its Activity for CO 2 Methanation
NiO and CeO 2 were prepared via flame spray pyrolysis. The specific surface area and total pore volume were 251 m 2 g –1 and 2.3 cm 3 g –1 for NiO and 338 m 2 g –1 and 3.3 cm 3 g –1 for CeO 2 , respectively. The high porosity and surface area of the NiO allowed deposition of small CeO 2 particles ( 〜 5 nm) by the impregnation of cerium acetate monohydrate. The particles were reduced using 5 % H 2 at 500 °C for 1 h which converted NiO to metallic Ni. During the reduction, the growth of Ni particles was hindered by CeO 2 particles. Consequently, the Ni size was relatively small ( 〜 20 nm) despite the extremely high Ni content (80 wt%), as observed by scanning transmission electron microscopy. In contrast, incorporation of Ni using nickel acetate tetrahydrate into the CeO 2 support resulted in formation of inhomogeneous Ni particles (20-100 nm) after H 2 reduction. H 2 chemisorption measurement showed the surface area of Ni particles in the former catalyst was 13.7 m 2 g –1 , which was 2.4 times larger than that in the latter catalyst. The former catalyst exhibited remarkable performance for CO 2 methanation (47 % CO 2 conversion at 250 °C), 2 times higher than in the latter catalyst.
期刊介绍:
“Journal of the Japan Petroleum Institute”publishes articles on petroleum exploration, petroleum
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