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Catalytic performances of Ni/mesoporous SiO_2 catalysts for dry reforming of methane to hydrogen 被引量:4
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作者 Fei Huang Rui Wang +3 位作者 Chao Yang hafedh driss Wei Chu Hui Zhang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2016年第4期709-719,共11页
Several mesoporous silicas with different morphologies were controllably prepared by sol-gel method with adjustable ratio of dual template, and they were further impregnated with aqueous solution of nickel nitrate, fo... Several mesoporous silicas with different morphologies were controllably prepared by sol-gel method with adjustable ratio of dual template, and they were further impregnated with aqueous solution of nickel nitrate, followed by calcination in air. The synthesized silica supports and supported nickel samples were characterized using N2-adsorption/desorption, X-ray diffraction (XRD), H2temperature-programmed reduction (H2-TPR), Scanning electron microscope (SEM), Transmission electron microscope (TEM) and thermo-gravimetric analysis (TGA-DTG) techniques. The Ni nanoparticles supported on shell-like silica are highly dispersed and yielded much narrower nickel particle-size than those on other mesoporous silica. The methane reforming with dioxide carbon reaction results showed that Ni nanoparticles supported on shell-like silica carrier exhibited the better catalytic performance and catalytic stability than those of nickel catalyst supported on other silica carrier. The thermo-gravimetric analysis on used nickel catalysts uncovered that catalyst deactivation depends on the type and nature of the coke deposited. The heterogeneous nature of the deposited coke was observed on nickel nanoparticles supported on spherical and peanut-like silica. Much narrower and lower TGA derivative peak was founded on Ni catalyst supported on the shell-like silica. ? 2016 Science Press 展开更多
关键词 Carbon Catalyst activity Catalyst deactivation CATALYSTS Catalytic reforming COKE Gravimetric analysis HYDROGEN Methane Nanoparticles Nickel Particle size Scanning electron microscopy Silica SOL gel process SOL GELS Solutions Thermogravimetric analysis Transmission electron microscopy X ray diffraction
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用于乙苯氧化脱氢制苯乙烯铝-硼催化剂:铝硼组成及制备方法对催化剂性能的影响(英文) 被引量:3
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作者 Nagaraju Pasupulety Muhammad A.Daous +2 位作者 Abdulrahim A.Al-Zahrani hafedh driss Lachezar A.Petrov 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第11期1758-1765,共8页
采用溶胶-凝胶(SG)法合成了不同摩尔比的Al-B催化剂(Al-10B与Al-35B).在450-500℃,乙苯(EB)接触时间为0.54 g-cat.s.cm-3的条件下,在氧气和水蒸气存在下对这些催化剂进行催化乙苯脱氢反应.利用NH3-TPD质谱分析了Al-B催化剂的酸性.扫描... 采用溶胶-凝胶(SG)法合成了不同摩尔比的Al-B催化剂(Al-10B与Al-35B).在450-500℃,乙苯(EB)接触时间为0.54 g-cat.s.cm-3的条件下,在氧气和水蒸气存在下对这些催化剂进行催化乙苯脱氢反应.利用NH3-TPD质谱分析了Al-B催化剂的酸性.扫描电镜图像显示,硼在氧化铝中负载量达15%(Al-15b)时仍分布很好,而在较高的硼含量(Al-25B和Al-35B)催化剂中观察到硼聚集.从本质上讲,在Al和Al-10B催化剂上观察到强度非常弱(Tmax≤125℃)的酸位,使得EB转化率和苯乙烯产率很低.另一方面,在Al-25B和Al-35B催化剂酸位较弱(Tmax≤180℃),因而EB转化率较高.然而,在弱-中等强度酸位的Al-15B催化剂上可以得到较高的苯乙烯产率(43.2%)和合理的EB转化率(46%).另外,采用共沉淀法(COP)和浸渍法(IMP)合成了Al-15B催化剂.IMP和COP催化剂的NH3-TPD-质谱分析结果发现,与NOx形成有关的酸位点在500℃时将EB转化率分别提高到66%和63%.然而,Al-B SG催化剂中的这些酸位降低,使得500℃时EB转化率为50%.当EB转化率为50%时,在Al-B IMP,Al-B COP和Al-SG催化剂上苯乙烯选择性分别为73%,82.5%和84%.因此,不同方法制备的Al-B催化剂,会产生不同强度和密度的酸位,从而影响苯乙烯的形成. 展开更多
关键词 铝-硼 氧化脱氢 乙苯 苯乙烯 共沉淀
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