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安秉濬,朴準勵,全學濟 全北大學校 基礎科學硏究所 1991 基礎科學 Vol.14 No.1
ZSM-5 제올라이트 촉매의 고체산 특성을 암모니아 승온 탈착법과 적외선 분광법에 의하여 조사하였다. HZSM-5의 암모니아 승온 탈착 곡선에는 α, β, γ의 세가지 상태가 나타나는데, γ-상태의 양은 실리카/알루미나 비가 클 수록 그리고 알칼리금속의 양이온 교환에 의하여 감소됨을 알았다. ZSM-5에 흡착시킨 피리딘의 적외선 흡수스펙트럼과 톨루엔의 알킬화반응으로부터 γ-상태는 Si-OH-Al의 수산기 즉 브뢴스테드산점에 기인하며 산촉매반응의 활성점으로 작용하는 것을 알았다. 또 알칼리양이온 교환시킨 ZSM-5의 암모니아, 피리딘 등의 염기와의 상호작용의 세기는 양이온 크기가 작아질수록 증가함을 알 수 있었다. Acidic properties of ZSM-5 zeolite catalysts were investigated by temperature-progarmmed desorption technique and ir spectroscopy. Ammonia t.p.d. pattern of HZSM-5 showed three different states, designated as α, β, and γ. The amount of γ-state decreased with increasing SiO_2/Al_2O_3 ratio, and upon cation-exchanging with alkali cations. from the ir absorption spectra of adsorbed pyridine and the reaction study of toluene alkylation, the γ-state could be explained to be due to the strong Bronsted acid sited of H-ZSM-5. Also they showed that the interaction between alkali cation-exchanged ZSM-5 and bases, i.e. NH_3 and pyridine, was increasing with decreasing the size of cations.
안병준,박준려,전학제,Byoung Joon Ahn,Joon Ryeo Park,Hakze Chon 대한화학회 1989 대한화학회지 Vol.33 No.2
ZSM-5 제올라이트 촉매의 고체산 특성을 암모니아 승온 탈착법과 적외선 분광법에 의하여 조사하였다. HZSM-5의 암모니아 승온 탈착 곡선에는 ${\alpha}$,${\beta}$,${\gamma}$의 세가지 상태가 나타나는데, ${\gamma}$-상태의 양은 실리카/알루미나 비가 클수록 그리고 알칼리 금속의 양이온 교환에 의하여 감소됨을 알았다. ZSM-5에 흡착시킨 피리딘의 적외선 흡수스펙트럼과 톨루엔의 알킬화반응으로부터 ${\gamma}$-상태는 Si-OH-Al의 수산기 즉 브뢴스테드산점에 기인하며 산촉매반응의 활성점으로 작용하는 것을 알았다. 또 알칼리양이온 교환시킨 ZSM-5의 암모니아, 피리딘 등의 염기와의 상호작용의 세기는 양이온 크기가 작아질수록 증가함을 알 수 있었다. Acidic properties of ZSM-5 zeolite catalysts were investigated by temperature-programmed desorption technique and ir spectroscopy. Ammonia t.p.d. pattern of HZSM-5 showed three different states, designated as ${\alpha}$,${\beta}$ and ${\gamma}$. The amount of ${\gamma}$-state decreased with increasing $SiO_2/Al_2O_3$ ratio, and upon cation-exchanging with alkali cations. From the ir adsorption spectra of absorbed pyridine and the reaction study of toluene alkylation, the ${\gamma}$-state could be explained to be due to the strong Bronsted acid sites of H-ZSM-5. Also they showed that the interaction between alkali cation-exchanged ZSM-5 and bases, i.e. $NH_3$ and pyridine, was increasing with decreasing the size of cations.
He-Xin Zhang,윤근병,이영주,박준려,이동호 한국고분자학회 2011 Macromolecular Research Vol.19 No.6
Polymerization of propylene was carried out using a MgCl_2-supported TiCl_4 catalyst in conjunction with triethylaluminium (TEA) as the cocatalyst and various types of alkoxy silane compounds as an external donor. The effect of the external donor on the performance of the catalyst with different internal donors was investigated. The polydispersity index (PDI) of polypropylene (PP) obtained with the diether and succinate based catalyst were decreased with the introduction of an external donor and the PDI increased for the phthalate based catalyst. The molecular weight and PDI increased with the introduction of an external donor. The highest PDI of PP was obtained by polymerization with di-n-propyldimethoxysilane (DnPDMS) as an external donor. In addition, a mixture of external donors was used to control the PDI of PP and the composition of the catalyst was examined after treated with TEA/external donor. Furthermore, the theoretical PDI value was calculated for a mixture of external donor systems. The PDI of PP could be controlled and predicted while retaining high activity, high isospecificity and high molecular weight by changing the structure of the external donor and/or their mixture.