检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:艾馨鹏[1] 岳宝华[2] 汪学广[1] 杨军[1] 鲁雄刚[1] 丁伟中[1]
机构地区:[1]上海大学,上海市现代冶金与材料制备重点实验室,上海200072 [2]上海大学理学院化学系,上海200444
出 处:《物理化学学报》2009年第8期1517-1522,共6页Acta Physico-Chimica Sinica
基 金:国家高技术研究发展计划(863)项目(2006AA11A189);国家科技支撑计划项目(2006BA103A05);上海市科学技术委员会重点项目(07DZ12036);上海市浦江人才计划(08PJ14059)资助~~
摘 要:采用分步浸渍法制备了MgO-Al2O3负载的Ni基催化剂,并运用N2吸附、X射线衍射(XRD)、透射电子显微镜(TEM)等手段进行表征.该催化剂用于甲苯或萘为焦油模拟化合物的高温焦炉煤气(COG)的常压加氢裂解反应,并考察了H2浓度、H2S对催化剂活性的影响.结果表明:催化剂还原后,表面形成均匀分散、直径为8-14nm的金属Ni纳米颗粒;在较低的水碳摩尔比(nH2O/nC=0.28)时,甲苯就能完全转化并选择性地加氢裂解形成CH4,测试的时间内(480min),催化剂没有明显的失活和积炭现象,显示出好的反应活性、稳定性和耐硫能力.制得的Ni/MgO-Al2O3催化剂有望应用于较低水含量(10%-15%(φ,体积分数))的高温焦炉煤气中焦油的直接转化.NiO/MgO-Al2O3 catalysts with different Ni contents were prepared by a two-step impregnation method and characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) and transmission electron microscopy (TEM). Results showed that metallic Ni nanoparticles with diameters of 8-14 nm were formed and homogenously dispersed on the surface of the catalysts after reduction at 800℃. The catalysts were used for the catalytic conversion of toluene as a model tar compound in hot coke oven gas (COG) and showed excellent catalytic activity, stability and sulfur tolerance. Toluene could be fully converted and selectively hydrogenated to CI-L even using a low molar ratio of water to carbon (nH2O/nc=0.28) at 800℃ and under ambient pressure. The existence of H2O in the feed gas greatly enhanced the conversion of toluene and contributed to CH4 formation. Under similar conditions, naphthalene was converted into light fuel gases. Effects of H2 concentration and H2S in the feed gas were discussed. The Ni/MgO-Al2O3 catalyst was promising for the hydrocracking of tar compounds in hot coke oven gas with a low H20 content of 10%- 15% (φ, volume fraction).
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.42