A Study on the Coking Sites of γ-Alumina Surface Using 1-Methylnaphthalene as the Model Reactant

被引:0
作者
Hu Anpeng [1 ]
Han Wei [1 ]
Zhang Le [1 ]
Long Xiangyun [1 ]
Li Mingfeng [1 ]
Nie Hong [1 ]
机构
[1] SINOPEC Res Inst Petr Proc, Beijing 100083, Peoples R China
关键词
1-methylnaphthalene; gamma-Al2O3; coking sites; chemical static adsorption; accelerated coking; COKE FORMATION; CATALYST DEACTIVATION; HYDRODESULFURIZATION; SULFUR;
D O I
暂无
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The support gamma-Al2O3 was treated with 1-methylnaphthalene as the model reactant by respectively using the chemical static adsorption method and the accelerated coking method to study the coking sites of gamma-Al2O3 surface. The carbon species formed on gamma-Al2O3 surface were analyzed by CAT-CS, TG-MS, IR-OH, and Py-IR techniques. The results of characterization by CAT-CS and TG-MS techniques indicated that the carbon species formed during the chemical static adsorption process is mainly composed of the reversibly adsorbed coke precursors with a lowly-condensed state, while that formed after the accelerated coking process is probably related with the irreversibly adsorbed coke deposits with a highly-condensed state. The results of characterization by IR-OH and Py-IR techniques further implied that the formation of the two kinds of carbon species, i.e., coke precursors and coke deposits, are closely related with the basic hydroxyl groups and the strong Lewis acid sites on gamma-Al2O3 surface. The results lead to a deep insight into the coking mechanism on the alumina surface.
引用
收藏
页码:37 / 43
页数:7
相关论文
共 26 条
[11]   Influence of the promoter's nature (nickel or cobalt) on the active phases 'Ni(Co)MoS' modifications during deactivation in HDS of diesel fuel [J].
Guichard, Bertrand ;
Roy-Auberger, Magalie ;
Devers, Elodie ;
Pichon, Christophe ;
Legens, Christelle ;
Lecour, Philippe .
CATALYSIS TODAY, 2010, 149 (1-2) :3-+
[12]   CATALYTIC ALUMINAS - SURFACE MODELS AND CHARACTERIZATION OF SURFACE SITES [J].
KNOZINGER, H ;
RATNASAMY, P .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1978, 17 (01) :31-70
[13]   Correlation of the deactivation of CoMo/Al2O3 in hydrodesulfurization with surface carbon species [J].
Koh, Jae Hyun ;
Lee, Jung Joon ;
Kim, Heeyeon ;
Cho, Ara ;
Moon, Sang Heup .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2009, 86 (3-4) :176-181
[14]   DRIFTS study of surface of γ-alumina and its dehydroxylation [J].
Liu, Xinsheng .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (13) :5066-5073
[15]   Deactivation patterns of Mo/Al2O3, Ni-Mo/Al2O3 and Ni-MoP/Al2O3 catalysts in atmospheric residue hydrodesulphurization [J].
Marafi, A. ;
Hauser, A. ;
Stanislaus, A. .
CATALYSIS TODAY, 2007, 125 (3-4) :192-202
[16]   FTIR spectroscopy of OH in olivine: A new tool in kimberlite exploration [J].
Matveev, S. ;
Stachel, T. .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2007, 71 (22) :5528-5543
[17]  
Miao Z, 2017, CHINA PET PROCESS PE, V19, P8
[18]  
SCARONI AW, 1985, APPL CATAL, V14, P173
[19]   LEWIS ACIDITY AND COKING OF HYDRODESULFURIZATION CATALYSTS [J].
SCARONI, AW ;
JENKINS, RG ;
UTRILLA, JR ;
WALKER, PL .
FUEL PROCESSING TECHNOLOGY, 1984, 9 (01) :103-108
[20]   Catalyst deactivation during upgrade of light catalytic cracking gas oil to ultralow-sulfur and low-aromatic diesel [J].
Tailleur, Roberto R. Galiasso .
ENERGY & FUELS, 2008, 22 (03) :1509-1518