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(M,Na)ZSM-5沸石合成中的阳离子效应 Ⅱ.正丁胺阳离子的行为 被引量:2

THE EFFECTS OF CATIONS ON SYNTHESIS OF ZSM-5 ZEOLITE Ⅱ. BEHAVIOR OFN-BTUYLAMINE IN ZSM-5 ZEOLITE SYNTHESiS
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摘要 本文用TG、MS、元素分析等方法研究了合成沸石烘干原粉中有机胺的存在状态。结果表明,沸石孔道中有机胺有两种状态,一种是物理吸咐态正丁胺,另一种是电荷补偿态的三丁基胺。并从孔道填充角度分析说明,三丁基胺作为模板剂有利于ZSM-5沸石的晶化。阶段取样实验证明,有机胺主要以电荷补偿阳离子形式构成三丁基胺正四面体结构,导向ZSM-5沸石核的生成。同时,正丁胺以物理吸咐态形式进入沸石孔道。酸性测定发现,正丁胺合成体系品化的ZSM-5沸石,强酸性中心主要产生于电荷补偿有机胺分解后生成的酸性中心。 Various techniques, such as TG, MS and elemental analysis etc., were used to investigate the behaviour of n-butylamine in ZSM-5 zeolite synthesis. Results showed that butylamines existed in two states in ZSM-5 channels: physically adsorbed n-butylamine and chargecompensating tributylamine. ZSM-5 channels were most effectively filled by butylamines in the crystallization process. The study of different crysallization stage demonstrated that charge-compensating amines directed the formation of ZSM-5 zeolite; while the physically adsorbed amines entered zeolite channels with the crystallization process. Acid messurement indicated that stronger acid sites were formed by decomposition of charge-compensating tributylamine, and the reason has also been discussed.
出处 《燃料化学学报》 EI CAS CSCD 北大核心 1990年第4期343-349,共7页 Journal of Fuel Chemistry and Technology
关键词 ZSM-5 沸石 合成 正丁胺 模板效应 ZSM-5 zoelite n-butylamine tributylamine strong acid center charge-compensating state
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参考文献2

  • 1陈韬,燃料化学学报,1990年,18卷,337页
  • 2宋天佑,石油学报,1983年,1卷,27页

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