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作 者:肖天存[1] 王海涛[1] 陈方[1] 鹿玉理[1] 安立敦[2] 王弘立[3]
机构地区:[1]山东大学环境工程系 [2]中国科学院兰州化学物理研究所 [3]中国科学院大连化学物理研究所
出 处:《催化学报》1998年第2期144-148,共5页
摘 要:改变硅源和晶化时间合成了系列SAPO5分子筛.用原位红外光谱和NH3TPD研究了不同样品的酸碱性,用TGDTA和MASNMR考察了硅源及晶化时间对分子筛模板剂的影响,评价了不同样品对正己烷裂解的催化活性.结果表明,SAPO5分子筛孔道不仅与模板剂的胺基有作用,而且与其甲基也有作用.以硅凝胶为硅源时,在48h内,延长晶化时间可使分子筛中硅含量和强酸中心数目增加,低温下正己烷裂解活性提高;晶化72h时,分子筛的酸性减弱,正己烷裂解活性降低.以正硅酸乙酯为硅源时,延长晶化时间可使SAPO5的酸性增强,正己烷裂解性能提高.A series of SAPO_5 have been synthesized by changing Si source and crystallization time. Using NH_3 as the probe molecule, the acidity of SAPO_5 was characterized by insitu IR. TGDTA and 13C MAS NMR were employed to study the effect of crystallization time on the state of template. The acidcatalytic performance of SAPO_5 was evaluated with n-hexane cracking. The results show that not only the amine group interacts with the channel of SAPO_5, but the methyl group interacts with the framework of SAPO_5. The 13C MAS NMR can be used to show the crystallinity of SAPO_5. Si sources have effects on the state of template, acidity and catalytic performance of SAPO_5. When using SiO_2 gel as Si source, within 48 h, prolonging the crystallization time can increase the Si content and the amount of acidity, and improve the activity for n-hexane cracking at lower temperature. When the crystallization time exceeds 48 h, the acidity and catalytic activity of SAPO_5 decrease. While using Si(OEt)_4 as Si source, the acidity and the catalytic activity of SAPO_5 rise with crystallization time.
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