GB787084A - Isomerization of xylene - Google Patents

Isomerization of xylene

Info

Publication number
GB787084A
GB787084A GB11602/55A GB1160255A GB787084A GB 787084 A GB787084 A GB 787084A GB 11602/55 A GB11602/55 A GB 11602/55A GB 1160255 A GB1160255 A GB 1160255A GB 787084 A GB787084 A GB 787084A
Authority
GB
United Kingdom
Prior art keywords
xylene
fraction
line
zone
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB11602/55A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
California Research LLC
Original Assignee
California Research LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by California Research LLC filed Critical California Research LLC
Publication of GB787084A publication Critical patent/GB787084A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C15/00Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
    • C07C15/02Monocyclic hydrocarbons
    • C07C15/067C8H10 hydrocarbons
    • C07C15/08Xylenes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/22Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
    • C07C5/27Rearrangement of carbon atoms in the hydrocarbon skeleton
    • C07C5/2729Changing the branching point of an open chain or the point of substitution on a ring
    • C07C5/2732Catalytic processes
    • C07C5/2735Catalytic processes with metal oxides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/14Purification; Separation; Use of additives by crystallisation; Purification or separation of the crystals

Abstract

<PICT:0787084/IV (b)/1> p-Xylene is produced by the isomerization of a mixture of xylene isomers consisting predominantly of o- and m-xylene and containing less than an equilibrium amount of p-xylene in which the mixture is fractionally distilled to separate an overhead fraction rich in m-xylene and a bottoms fraction rich in o-xylene, and in which the overhead fraction is contacted with a silica-alumina catalyst at 700-1000 DEG F. and at a space velocity of 0.5-5.0 v/v/hour and the bottoms fraction is separately contacted with a silica-alumina catalyst at a temperature of 100-150 DEG F. higher than that employed in treating the overhead fraction and at approximately the same space velocity. The catalysts are preferably periodically regenerated by contacting with a free oxygen-containing gas and passing steam through the catalyst for a period of 2-20 minutes immediately subsequent to the regeneration step. In an example, a feed consisting of ethylbenzene 5.8 weight per cent, para-xylene 18.6, meta-xylene 38.4, ortho-xylene 26.0, and C7 and C9 hydrocarbons and paraffins 11.2, is passed through a line 1 into a crystallization zone 2 where a part of the p-xylene is crystallized at a temperature of -75 DEG to -120 DEG F., the crystals being separated by a centrifugal filter 4. The mother liquor is removed by line 6 and a fractionated in zone 7 into a fraction containing chiefly m-xylene which is removed through line 8 and is isomerized in zone 14 at a temperature of 700-1000 DEG F. while the higher boiling fraction is removed through line 13 and isomerized at from 100-150 DEG F. higher than the temperature used for the overhead fraction. The isomerized mixture is distilled in zone 19 from which ethylbenzene and lighter components are taken off by line 24. A fraction consisting chiefly of m- and p-xylene is removed by line 25 and a fraction consisting predominantly of o-xylene by line 26.
GB11602/55A 1954-05-03 1955-04-21 Isomerization of xylene Expired GB787084A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US787084XA 1954-05-03 1954-05-03

Publications (1)

Publication Number Publication Date
GB787084A true GB787084A (en) 1957-12-04

Family

ID=22145747

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11602/55A Expired GB787084A (en) 1954-05-03 1955-04-21 Isomerization of xylene

Country Status (1)

Country Link
GB (1) GB787084A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009117487A2 (en) 2008-03-18 2009-09-24 Gtc Technology, Lp Improved systems and processes for the production of isophthalic acid and terephthalic acid
CN113045379A (en) * 2021-03-31 2021-06-29 江苏正丹化学工业股份有限公司 Method for co-producing mesitylene and durene by alkylation-isomerization of C8 or C9 aromatic hydrocarbon
CN114534771A (en) * 2022-03-03 2022-05-27 大庆亿鑫化工股份有限公司 Isomerization catalyst of mixed xylene and separation method of o-xylene

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009117487A2 (en) 2008-03-18 2009-09-24 Gtc Technology, Lp Improved systems and processes for the production of isophthalic acid and terephthalic acid
EP2276720A2 (en) * 2008-03-18 2011-01-26 Gtc Technology, Lp Improved systems and processes for the production of isophthalic acid and terephthalic acid
JP2011517667A (en) * 2008-03-18 2011-06-16 ジーティーシー テクノロジー エルピー Improved systems and methods for the production of isophthalic acid and terephthalic acid
EP2276720A4 (en) * 2008-03-18 2012-05-02 Gtc Technology Lp Improved systems and processes for the production of isophthalic acid and terephthalic acid
RU2496764C2 (en) * 2008-03-18 2013-10-27 ДжиТиСи ТЕКНОЛОДЖИ, ЭлПи Method (versions) and systems for producing isophthalic acid and terephthalic acid
US9040746B2 (en) 2008-03-18 2015-05-26 Gtc Technology Us, Llc Systems and processes for the production of isophthalic acid and terephthalic acid
CN105732256B (en) * 2008-03-18 2019-06-28 Gtc技术有限公司 Method for producing M-phthalic acid and terephthalic acid (TPA)
CN113045379A (en) * 2021-03-31 2021-06-29 江苏正丹化学工业股份有限公司 Method for co-producing mesitylene and durene by alkylation-isomerization of C8 or C9 aromatic hydrocarbon
CN113045379B (en) * 2021-03-31 2023-09-22 江苏正丹化学工业股份有限公司 Method for co-producing mesitylene and durene by C8 aromatic hydrocarbon alkylation-isomerization
CN114534771A (en) * 2022-03-03 2022-05-27 大庆亿鑫化工股份有限公司 Isomerization catalyst of mixed xylene and separation method of o-xylene
CN114534771B (en) * 2022-03-03 2022-09-16 大庆亿鑫化工股份有限公司 Isomerization catalyst for mixed xylene and separation method of o-xylene

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