Influence of combined acid treatment on physico-chemical characteristics of ultrastable zeolite Y and on its catalytic properties in the disproportionation of ethylbenzene

被引:10
作者
Gomes, ACL
SAguiar, EF
CardosoMenezes, SC
Cardoso, D
机构
[1] UNIV FED SAO CARLOS,DEPT CHEM ENGN,BR-13565905 SAO CARLOS,SP,BRAZIL
[2] PETROBRAS SA,CENPES,RIO JANEIRO,BRAZIL
关键词
ethylbenzene; disproportionation; USY zeolite; dealumination (acid treatment);
D O I
暂无
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 [物理化学]; 081704 [应用化学];
摘要
Ultrastable zeolites (USY) have been treated with sulphuric and/or phosphoric acids, aiming at the determination of the interaction of both acids with either framework (FAL) or extraframework (EFAL) aluminas, as well as the effect of such modifications on catalytic properties in ethylbenzene disproportionation. Zeolites have been characterized by means of several physicochemical techniques (XRD, XRF; FTIR, Si-29, Al-27 and P-31-MAS/NMR, nitrogen adsorption and AA). Results revealed that the treatment with H2SO4 removes EFAL located in supercavities without attacking the zeolitic framework. Treatment with H3PO4 incorporates P in two quite distinct ways: as a monomeric phosphate associated to framework aluminium atoms (for low EFAL concentrations) and as a polymeric phosphate originated from the reaction of EFAL with H2PO4 (for high EFAL concentrations). Regarding catalytic properties, initial activities are higher for H2SO4 leached samples when compared to those which have just been calcined. Nevertheless,initial activities of samples treated with H3PO4 depend strongly on the P2O5 content incorporated into the zeolite. With respect to isomers (ortho-, meta- and para-diethylbenzenes) generally formed in this disproportionation reaction, no considerable para-selectivity has been observed.
引用
收藏
页码:373 / 385
页数:13
相关论文
共 17 条
[1]
DETERMINATION OF FRAMEWORK AND NONFRAMEWORK ALUMINUM IN HY DEALUMINATED ZEOLITES BY X-RAY PHOTOELECTRON-SPECTROSCOPY [J].
CORMA, A ;
FORNES, V ;
PALLOTA, O ;
CRUZ, JM ;
AYERBE, A .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1986, (04) :333-334
[2]
ORTHOPHOSPHORIC ACID INTERACTIONS WITH ULTRASTABLE ZEOLITE-Y - INFRARED AND NMR-STUDIES [J].
CORMA, A ;
FORNES, V ;
KOLODZIEJSKI, W ;
MARTINEZTRIGUERO, LJ .
JOURNAL OF CATALYSIS, 1994, 145 (01) :27-36
[3]
FT-IR AND SOLID-STATE NMR INVESTIGATION OF PHOSPHORUS PROMOTED HYDROTREATING CATALYST PRECURSORS [J].
DECANIO, EC ;
EDWARDS, JC ;
SCALZO, TR ;
STORM, DA ;
BRUNO, JW .
JOURNAL OF CATALYSIS, 1991, 132 (02) :498-511
[4]
Surfaces of solids XII An absolute method for the determination of the area of a finely divided crystalline solid [J].
Harkins, WD ;
Jura, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 :1362-1366
[5]
INNOV T, 1990, ZEOLITES CARACTERIST
[6]
KAENDING WW, 1985, J CATAL, V95, P512
[7]
CONVERSION OF ALKYLBENZENES OVER ZEOLITE CATALYSTS .2. DISPROPORTIONATION OF ETHYLBENZENE OVER FAUJASITE-TYPE ZEOLITES [J].
KARGE, HG ;
HATADA, K ;
ZHANG, Y ;
FIEDOROW, R .
ZEOLITES, 1983, 3 (01) :13-21
[8]
CONVERSION OF ALKYLBENZENES OVER ZEOLITE CATALYSTS .1. DEALKYLATION AND DISPROPORTIONATION OF ETHYLBENZENE OVER MORDENITES [J].
KARGE, HG ;
LADEBECK, J ;
SARBAK, Z ;
HATADA, K .
ZEOLITES, 1982, 2 (02) :94-102
[9]
TOLUENE DISPROPORTIONATION REACTION OVER MODIFIED HY AND LAHY CATALYSTS [J].
LEU, LJ ;
KANG, BC ;
WU, ST ;
WU, JC .
APPLIED CATALYSIS, 1990, 63 (01) :91-106
[10]
STUDIES ON PORE SYSTEMS IN CATALYSTS .V. T METHOD [J].
LIPPENS, BC ;
DEBOER, JH .
JOURNAL OF CATALYSIS, 1965, 4 (03) :319-&