Patent classifications
C07C5/2775
Method for the isomerizing dehydration of a non-linear primary alcohol feedstock in the presence of water injection and a catalyst comprising a FER or MFS zeolite
A process for the isomerizing dehydration of a feedstock including a primary monoalcohol, alone or as a mixture, of formula R—CH.sub.2—OH, wherein R is a nonlinear alkyl radical of general formula C.sub.nH.sub.2n+1 where n is an integer between 3 and 20, the process taking place in the gas phase at a weighted average temperature between 275° C. and 400° C., at a pressure between 0.3 MPa and 1 MPa and at a WWH (weight per weight per hour) between 5 and 10 h.sup.−1, in the presence of a catalyst containing at least one silicic binder and at least one zeolite having at least one series of channels, the opening of which is defined by a ring of 8 oxygen atoms (8MR), process wherein vaporized feedstock entering the reactor has a weight content of water of from 4% to 35%.
Molecular sieve SSZ-94, catalyst, and methods of use thereof
The present application pertains to family of new crystalline molecular sieves designated SSZ-94. Molecular sieve SSZ-94 is structurally similar to sieves falling within the MTT structure type such as SSZ-32x, SSZ-32, ZSM-23, EU-13, ISI-4, and KZ-1 family of molecular sieves. SSZ-94 is characterized as having magnesium.
ZSM-35 MOLECULAR SIEVE AND PRODUCTION METHOD THEREFOR, ISOMERIZATION CATALYST AND PRODUCTION METHOD THEREFOR, AND ISOMERIZATION METHOD
The present disclosure provides a ZSM-35 molecular sieve and a preparation method therefor, an isomerization catalyst and a preparation method therefor, and an isomerization method. The preparation method for a ZSM-35 molecular sieve comprises: mixing a silicon source, an aluminum source, an alkali, a template agent and water, then adding a polyacrylamide thereto, and performing crystallization on same twice to obtain a ZSM-35 molecular sieve. The present disclosure further provides an isomerization catalyst prepared from the ZSM-35 molecular sieve and a preparation method therefor, and an isomerization method.
ZSM-35 MOLECULAR SIEVE AND PRODUCTION METHOD THEREFOR, ISOMERIZATION CATALYST AND PRODUCTION METHOD THEREFOR, AND ISOMERIZATION METHOD
The present disclosure provides a ZSM-35 molecular sieve and a preparation method therefor, an isomerization catalyst and a preparation method therefor, and an isomerization method. The preparation method for a ZSM-35 molecular sieve comprises: mixing a silicon source, an aluminum source, an alkali, a template agent and water, then adding a polyacrylamide thereto, and performing crystallization on same twice to obtain a ZSM-35 molecular sieve. The present disclosure further provides an isomerization catalyst prepared from the ZSM-35 molecular sieve and a preparation method therefor, and an isomerization method.
Modified USY zeolitic catalyst for isomerization of alkylated aromatics, and method for isomerization of alkylated aromatics
The present invention relates to a catalyst for isomerization of alkylated aromatics such as mixed xylenes, using xylene isomerization catalyst particles including post-framework modified USY zeolite in which zirconium atoms and/or titanium atoms and/or hafnium atoms form a part of a framework of an ultra-stable Y-type zeolite.
Modified USY zeolitic catalyst for isomerization of alkylated aromatics, and method for isomerization of alkylated aromatics
The present invention relates to a catalyst for isomerization of alkylated aromatics such as mixed xylenes, using xylene isomerization catalyst particles including post-framework modified USY zeolite in which zirconium atoms and/or titanium atoms and/or hafnium atoms form a part of a framework of an ultra-stable Y-type zeolite.
Apparatus and process for converting aromatic compounds by benzene alkylation with ethanol
Apparatus and process for converting aromatic compounds, comprising/using: a fractionating train (4-7) suitable for extracting at least one benzene-comprising fraction (22), one toluene-comprising fraction (23) and one fraction (24) comprising xylenes and ethylbenzene from the feedstock (2); a xylene separating unit (10) suitable for treating the fraction comprising xylenes and ethylbenzene and producing a para-xylene-comprising extract (39) and a raffinate (40) comprising ortho-xylene, meta-xylene and ethylbenzene; an isomerizing unit (11) for treating the raffinate and producing a para-xylene-enriched isomerizate (42), which is sent to the fractionated train; and an alkylating reaction section (13) for treating at least part of the benzene-comprising fraction with an ethanol source (30) and producing an alkylation effluent (31) comprising ethylbenzene, which is sent to the isomerizing unit.
Method for separating non-linear olefins from an olefin feed by reactive distillation
The present invention relates to a process for treating, by reactive distillation, an olefinic feedstock comprising linear olefins containing n carbon atoms, and branched olefins, the branched olefins comprising tertiary branched olefins, for example a mixture of n-butenes and of tertiary branched olefins comprising isobutene, so as to produce an olefinic effluent with a mass content of tertiary branched olefin of less than or equal to 3% by weight and a heavy hydrocarbon effluent, said process comprising the feeding of a reactive distillation section with said olefinic feedstock and with an alcohol feedstock comprising a primary alcohol, said reactive distillation section comprising a column composed at least of an upper reflux zone into which is introduced said alcohol feedstock, comprising, for example, ethanol, an intermediate reaction zone comprising at least 6 reactive doublets, and a lower fractionation zone at the level of which said section is fed with said olefinic feedstock, said reactive distillation section being operated at a relative pressure of between 0.3 and 0.5 MPa, a column head temperature of between 40° C. and 60° C., with a reflux ratio of between 1.8 and 2.2.
Method for separating non-linear olefins from an olefin feed by reactive distillation
The present invention relates to a process for treating, by reactive distillation, an olefinic feedstock comprising linear olefins containing n carbon atoms, and branched olefins, the branched olefins comprising tertiary branched olefins, for example a mixture of n-butenes and of tertiary branched olefins comprising isobutene, so as to produce an olefinic effluent with a mass content of tertiary branched olefin of less than or equal to 3% by weight and a heavy hydrocarbon effluent, said process comprising the feeding of a reactive distillation section with said olefinic feedstock and with an alcohol feedstock comprising a primary alcohol, said reactive distillation section comprising a column composed at least of an upper reflux zone into which is introduced said alcohol feedstock, comprising, for example, ethanol, an intermediate reaction zone comprising at least 6 reactive doublets, and a lower fractionation zone at the level of which said section is fed with said olefinic feedstock, said reactive distillation section being operated at a relative pressure of between 0.3 and 0.5 MPa, a column head temperature of between 40° C. and 60° C., with a reflux ratio of between 1.8 and 2.2.
Desilicated ZSM-5 Catalysts for Xylene Isomerization
A method of making a xylene isomerization catalyst comprises the steps of (i) contacting a ZSM-5 zeolite starting material having a silica to alumina molar ratio of 20 to 50 and having a mesopore surface area in the range of 50 m.sup.2/gram to 200 m.sup.2/gram in a reactor with a base to provide an intermediate zeolite material; (ii) recovering the intermediate ZSM-5 zeolite material of step (i); (iii) contacting the intermediate zeolite material with an acid to provide an acid treated ZSM-5 zeolite product; (iv) recovering the acid treated ZSM-5 zeolite material; and (v) calcining the acid treated ZSM-5 zeolite material to provide a desilicated ZSM-5 zeolite product having a silica to alumina molar ratio of 20 to 150 and having a mesopore surface area in the range of 100 m.sup.2/gram to 400 m.sup.2/gram.