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Featured researches published by Tianxi Cai.


Catalysis Today | 1999

Studies of a new alkene oligomerization catalyst derived from nickel sulfate

Tianxi Cai

Abstract NiSO4/γ-Al2O3 shows very high catalytic activity in alkene oligomerization with good selectivity for dimers. Its acidity plays a very important role in the catalytic behavior. However, it is the acid site with an acid strength of H0≤−3.0 that is related to the oligomerization of alkenes. Comparatively strong acidity is produced through the interaction of sulfate anions and γ-Al2O3 during calcination. Ni(II) is partially reduced to Ni(I) by reacting with ethene and propene at ambient temperature or evacuation at high temperatures. Dimerization of ethene can be considered as coordination catalysis at active sites of Ni(I), while oligomerization of propene proceeds via dual catalysis due to both coordination catalysis and acid catalysis. But-1-ene is catalytically oligomerized via mainly acid catalysis. Thus, it can be concluded that as the number of carbon atoms of the alkenes increases, the mechanism of oligomerization of the alkene over the catalyst shifts from coordination catalysis to acid catalysis.


Reaction Kinetics and Catalysis Letters | 2003

Selective hydrogenation of crotonaldehyde over raney cobalt catalysts modified with heteropolyacid salts

Baijun Liu; Tianxi Cai

RCo-based catalysts were modified with Keggin type heteropolyacid salts, including alkali, alkaline earth and transition metal salts. The selective hydrogenation of crotonaldehyde was investigated over these catalysts. The selectivities to crotyl alcohol can be improved on all modified catalysts. Among them, the catalyst modified with copper salts of 12-molybdophosphates shows the best performance in improving the selectivity.


Reaction Kinetics and Catalysis Letters | 2002

A dynamic study of isomerization on MoOx catalyst

Yingjun Wang; Xinping Wang; Song-Hai Chai; Tianxi Cai

The dynamics of n-heptane isomerization on the reduced MoO3 catalyst have been studied in a fixed bed flow reactor. In the reaction temperature ranging from 523 to 673 K, the apparent energy for n-heptane isomerization obtained from the Arrhenius plot was 49.3 kJ/mol. At 573 K, the reaction orders of 0.33 in n-heptane and 0.35 in H2 have been obtained.


Journal of Colloid and Interface Science | 2006

The study of thiophene adsorption onto La(III)-exchanged zeolite NaY by FT-IR spectroscopy

Fuping Tian; Weicheng Wu; Zongxuan Jiang; Changhai Liang; Yongxing Yang; Pinliang Ying; Xiuping Sun; Tianxi Cai; Can Li


Catalysis Today | 2004

n-Heptane isomerization over mesoporous MoOx and Ni–MoOx catalysts

Xinping Wang; Can Li; Yingjun Wang; Tianxi Cai


Archive | 2008

Method for preparing adamantine on solid acid catalyst

Min Ji; Tianxi Cai; Min He; Xiuyuan Li; Youjia Zhang; Fuping Tian


Catalysis Today | 2001

A study on structural suitability of immobilized aluminum chloride catalyst for isobutene polymerization

Tianxi Cai; Min He; Xianzhe Shi; Xinping Wang; Dongxiu Han; Lianhai Lü


Chinese Journal of Catalysis | 2005

Deep Desulfurization of Gasoline by Adsorption on Mesoporous MCM-41

Fuping Tian; Zongxuan Jiang; Changhai Liang; Yongxue Li; Tianxi Cai; Can Li


Reaction Kinetics and Catalysis Letters | 2005

Highly active and stable immobilized aluminium chloride catalyst for alkylation of benzene with 1-dodecene

Lijuan Shang; Min Ji; Tianxi Cai; Weijun Shan; Min He; Shan Jiang


Chinese Journal of Catalysis | 2005

Adsorption of sulfur-containing compounds from FCC gasoline on cerium-exchanged Y zeolite

Fuping Tian; Weicheng Wu; Zongxuan Jiang; Yan Yang; Tianxi Cai; Can Li

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Can Li

Dalian Institute of Chemical Physics

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Min Ji

Dalian University of Technology

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Fuping Tian

Dalian Institute of Chemical Physics

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Zongxuan Jiang

Dalian Institute of Chemical Physics

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Weicheng Wu

Dalian Institute of Chemical Physics

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Xinping Wang

Dalian University of Technology

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Changhai Liang

Dalian University of Technology

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Min He

Dalian University of Technology

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Yan Yang

Dalian Institute of Chemical Physics

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Yingjun Wang

Dalian University of Technology

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