Synthesis of the composite material Y/ASA and its catalytic performance for the cracking of n-decane

被引:40
|
作者
Meng, Qinglei [1 ]
Liu, Baijun [1 ]
Piao, Jiarui [2 ]
Liu, Qiwu [2 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Key Lab Catalysis, CNPC,Coll Chem Engn, Beijing 102249, Peoples R China
[2] PetroChina, PetroChem Res Inst, Beijing 100195, Peoples R China
关键词
Y/ASA composite; Wrapping; Bronsted acid site; Mesopore; n-Decane; Catalytic cracking; TEMPERATURE-PROGRAMMED DESORPTION; AMORPHOUS SILICA-ALUMINA; PORE-SIZE DISTRIBUTION; BRONSTED ACIDITY; MECHANICAL MIXTURE; EXTERNAL SURFACE; MOLECULAR-SIEVES; PROBE MOLECULES; Y-ZEOLITE; IRMS-TPD;
D O I
10.1016/j.jcat.2012.03.002
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Y/ASA composite was successfully prepared by wrapping NaY zeolite with small-crystal size in amorphous silica-alumina (ASA) gel. Characterization results show that bonding action between zeolite Y and ASA contributes new acid sites in HY/ASA, which are responsible for its higher activity in the catalytic cracking of n-decane and light diesel, comparing with the mixture-derived catalysts. HY/ASA catalyst possesses larger surface area and mesoporous volume and uniform slit-shaped mesopores, which are beneficial to the diffusion of the products and responsible for higher yield of the middle distillates. The smaller zeolite Y crystallites in Y/ASA lead to more contact points between Y crystallites and ASA and thus provide more new acid sites for the HY/ASA catalyst. The high conversion of n-decane and yield of middle distillates over the HY/ASA catalyst can be ascribed to its acid quantity and super pore structure. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:55 / 64
页数:10
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