首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Structure of alumina supported vanadia catalysts for oxidative dehydrogenation of propane prepared by flame spray pyrolysis
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Structure of alumina supported vanadia catalysts for oxidative dehydrogenation of propane prepared by flame spray pyrolysis

机译:火焰喷雾热解法制得的丙烷氧化丙烷脱氢氧化铝催化剂的结构

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A series of five vanadia on alumina catalysts for oxidative dehydrogenation of propane to propene were synthesized by flame spray pyrolysis (FSP) using vanadium(IH)acetylacetonate and alu-minium(IH)acetylacetonate dissolved in toluene as precursors. The vanadium loading was 2, 3, 5, 7.5 and 10 wt.%. The catalysts were subsequently characterized by BET surface area, X-ray diffraction (XRD), Raman, UV-vis diffuse reflectance and X-ray absorption spectroscopy (XAS) as well as measurement of the catalytic performance. The catalysts had specific surface areas from 143 to 169 m~2/g corresponding to average particles diameters from 9.0 to 10.9nm and apparent vanadia surface densities from 1.4 to 8.4 VO_xm~2. The only crystalline phase detected by XRD was γ-Al2O3, except at 10wt.% vanadium where traces of crystalline vanadia were observed. Raman spectroscopy showed vanadia monomers at 2 and 3 wt.% V( 1.4 and 2.1 VO_xm~2), a mixture of vanadia oligomers and monomers at 5 wt.% V (3.6 VO_xm~2) and mainly oligomers at 7.5 and 10wt.% V (6.0 and 8.4 VO_xm~2). Diffuse reflectance UV-vis and extended X-ray absorption fine structure (EXAFS) spectroscopy measurements supported the results of Raman spectroscopy. In situ X-ray absorption near edge structure (XANES) spectroscopy showed that the vanadia can be reduced when operating at low oxygen concentrations. The catalyst performance was determined in fixed bed reactors with an inlet gas composition of C3H8/O2/N2 = 5/25/70. The main products were propene, CO and CO2, with traces of ethene and acrolein. Comparing propene selectivity as function of propane conversion the most selective catalysts were the 2 and 3 wt.% V samples, which contained mostly vanadia monomers according to Raman spectroscopy. The best propene yield of 12% was obtained with the 2 wt.% vanadium catalyst while the best space time yield of 0.78 g_(Propene)/(g_(cat)·h) at 488 °C was obtained with the 3 wt.% V catalyst.
机译:通过火焰喷雾热解(FSP),以溶解在甲苯中的乙酰丙酮钒(IH)和乙酰丙酮铝(IH)为原料,通过火焰喷雾热解(FSP)合成了五种钒在氧化铝上催化丙烷氧化成丙烯的催化剂。钒载量为2、3、5、7.5和10重量%。随后通过BET表面积,X射线衍射(XRD),拉曼,UV-可见漫反射率和X射线吸收光谱法(XAS)以及催化性能的测量来表征催化剂。催化剂的比表面积为143-169m 2 / g,对应于平均粒径为9.0-10.9nm,表观钒的表面密度为1.4-8.4VO_x / nm 2。用XRD检测到的唯一结晶相是γ-Al2O3,除了钒含量为10wt%时,其中观察到痕量的结晶钒。拉曼光谱显示钒单体的含量为2和3 wt。%(1.4和2.1 VO_x / nm〜2),钒低聚物和单体的混合物为5 wt。%V(3.6 VO_x / nm〜2)和主要为7.5的低聚物和10wt。%V(6.0和8.4 VO_x / nm〜2)。漫反射紫外可见光谱和扩展的X射线吸收精细结构(EXAFS)光谱测量结果支持了拉曼光谱的结果。原位X射线吸收近边缘结构(XANES)光谱表明,在低氧浓度下操作时,钒可以还原。在固定床反应器中,入口气体组成为C3H8 / O2 / N2 = 5/25/70的条件下确定催化剂的性能。主要产品是丙烯,一氧化碳和二氧化碳,以及微量的乙烯和丙烯醛。比较丙烯选择性与丙烷转化率的函数,最有选择性的催化剂是2和3 wt%的V样品,根据拉曼光谱法,这些样品主要包含钒单体。使用2 wt。%的钒催化剂可获得12%的最佳丙烯收率,而使用3 wt。%的钒在488°C下可获得0.78 g_(丙烯)/(g_(cat)·h)的最佳时空产率。 V催化剂。

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