Song Ki Chang, Kim Joo Hyun, Kim Jin Han, Jung Kyeong Youl, Park Young-Kwon, Jeon Jong-Ki
Department of Chemical Engineering, Kongju National University, Cheonan, 330-717 Korea.
J Nanosci Nanotechnol. 2011 Jul;11(7):6312-7. doi: 10.1166/jnn.2011.4417.
The objective of the present study is to investigate the catalytic performance of mesoporous alumina that were prepared via spray pyrolysis for double bond migration from 2-butene to 1-butene. The mesoporous alumina particles were prepared via spray pyrolysis by changing the types of organic surfactants and Al precursors. The texture and acidic properties of mesoporous alumina were analyzed through N2 adsorption, SEM, ammonia-temperature programmed desorption, and FT-IR of adsorbed pyridine. The morphologies and texture properties of the mesoporous alumina were found to have been strongly influenced by the combination of the Al precursor and the structure-directing agents. The mesoporous alumina samples had two kinds of acidic sites: a Lewis acid site and a H-bonded weak acid site. 1-Butene was produced selectively through double bond migration of 2-butene over all of the mesoporous alumina catalysts. The catalyst prepared by using a chloride compound as an aluminium precursor and CTAC as a structure-directing agent showed the highest activity in the double bond migration of 2-butene, which was attributed to its large surface area and an overall high amount of acid sites.
本研究的目的是研究通过喷雾热解制备的介孔氧化铝对2-丁烯双键迁移至1-丁烯的催化性能。通过改变有机表面活性剂和铝前驱体的类型,采用喷雾热解制备介孔氧化铝颗粒。通过N2吸附、扫描电子显微镜(SEM)、氨程序升温脱附以及吸附吡啶的傅里叶变换红外光谱(FT-IR)对介孔氧化铝的织构和酸性性质进行分析。发现介孔氧化铝的形态和织构性质受到铝前驱体和结构导向剂组合的强烈影响。介孔氧化铝样品有两种酸性位点:路易斯酸位点和氢键结合的弱酸位点。在所有介孔氧化铝催化剂上,通过2-丁烯的双键迁移选择性地生成了1-丁烯。以氯化物化合物作为铝前驱体、十六烷基三甲基氯化铵(CTAC)作为结构导向剂制备的催化剂在2-丁烯双键迁移中表现出最高活性,这归因于其较大的表面积和总体较高的酸位点数量。