GB998186A - Process of maintaining the activity and/or regenerating the activity of used or spent acid activated montmorillonite catalyst - Google Patents

Process of maintaining the activity and/or regenerating the activity of used or spent acid activated montmorillonite catalyst

Info

Publication number
GB998186A
GB998186A GB2910361A GB2910361A GB998186A GB 998186 A GB998186 A GB 998186A GB 2910361 A GB2910361 A GB 2910361A GB 2910361 A GB2910361 A GB 2910361A GB 998186 A GB998186 A GB 998186A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
catalyst
alkylation
activity
treating
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
GB2910361A
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.)
GAF Chemicals Corp
Original Assignee
General Aniline and Film Corp
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 General Aniline and Film Corp filed Critical General Aniline and Film Corp
Publication of GB998186A publication Critical patent/GB998186A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/20Regeneration or reactivation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Acid activated clay catalysts (bentonite or montmorillonite) used in the alkylation of phenols with olefinic hydrocarbons are reactivated by separating the catalyst and treating with a compound which may be an olefinic hydrocarbon of 3-18 carbon atoms, an alkyl alcohol of 1-6 carbon atoms, ketones of 3-11 carbon atoms, ethers of 6-10 carbon atoms, esters of alkyl alcohols of 1-6 carbon atoms with saturated and unsaturated organic mono-carboxylic acids of 2-17 carbon atoms, or organic acids of 2-3 carbon atoms at a temperature ranging from ambient to 200 DEG C. Alternatively the catalyst may be regenerated in situ by adding one of the above compounds near the completion of the alkylation process and further treating at 70-150 DEG C. for 10-20 minutes.ALSO:In the alkylation of phenolic compounds with olefinic hydrocarbons using acid activated clay catalysts (bentonite or montmorillonite) the activity of the catalyst is maintained by separating the catalyst and treating with a compound which may be an olefinic hydrocarbon of 3-18 carbon atoms, an alkyl alcohol of 1-6 carbon atoms, ketones of 3-11 carbon atoms, ethers of 6-10 carbon atoms, esters of alkyl alcohols of 1-6 carbon atoms with saturated and unsaturated organic mono-carboxylic acids of 2-17 carbon atoms, or organic acids of 2-3 carbon atoms at a temperature ranging from ambient to 200 DEG C. A modification of the process comprises the addition of one of the above compounds to the reaction vessel near the completion of the reaction followed by heating at 70-150 DEG C. for 10-20 minutes.ALSO:Acid activated clay catalysts (bentonite or montmorillonite) used in the alkylation of phenols with olefinic hydrocarbons are reactivated by separating the catalyst and treating with a compound which may be an olefinic hydrocrabon of 3-18 carbon atoms, an alkyl alcohol of 1-6 carbon atoms, ketones of 3-11 carbon atoms, ethers of 6-10 carbon atoms, esters of alkyl alcohols of 1-6 carbon atoms with saturated and unsaturated organic monocarboxylic acids of 2-17 carbon atoms, or organic acids of 2-3 carbon atoms at a temperature ranging from ambient to 200 DEG C. A modification of the process comprises the regeneration of the catalyst in situ by adding one of the above compounds to the reaction vessel near the completion of the alkylation and further treating at 70-150 DEG C. for 10-20 minutes.
GB2910361A 1960-09-06 1961-08-11 Process of maintaining the activity and/or regenerating the activity of used or spent acid activated montmorillonite catalyst Expired GB998186A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US5391160A 1960-09-06 1960-09-06

Publications (1)

Publication Number Publication Date
GB998186A true GB998186A (en) 1965-07-14

Family

ID=21987373

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2910361A Expired GB998186A (en) 1960-09-06 1961-08-11 Process of maintaining the activity and/or regenerating the activity of used or spent acid activated montmorillonite catalyst

Country Status (2)

Country Link
BE (1) BE607350A (en)
GB (1) GB998186A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0352505A1 (en) * 1988-07-16 1990-01-31 Bayer Ag Method for the production of thymol
EP0370343A1 (en) * 1988-11-25 1990-05-30 Bayer Ag Method for the production of 4-methyl-2-cyclohexylphenol
WO1991001804A1 (en) * 1989-07-31 1991-02-21 Exxon Chemical Patents Inc. Process for regenerating a catalyst and resultant regenerated catalyst and production of olefins by catalytic ether decomposition using regenerated catalyst
EP3064273A1 (en) * 2015-03-03 2016-09-07 Chemtura Corporation Regeneration of clay catalysts for alkylation of aromatic rings

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0352505A1 (en) * 1988-07-16 1990-01-31 Bayer Ag Method for the production of thymol
US5030770A (en) * 1988-07-16 1991-07-09 Bayer Aktiengesellschaft Process for the preparation of thymol
EP0370343A1 (en) * 1988-11-25 1990-05-30 Bayer Ag Method for the production of 4-methyl-2-cyclohexylphenol
US4990687A (en) * 1988-11-25 1991-02-05 Bayer Aktiengesellschaft Preparation of 4-methyl-2-cyclohexylphenol
WO1991001804A1 (en) * 1989-07-31 1991-02-21 Exxon Chemical Patents Inc. Process for regenerating a catalyst and resultant regenerated catalyst and production of olefins by catalytic ether decomposition using regenerated catalyst
US5043518A (en) * 1989-07-31 1991-08-27 Exxon Chemical Patents Inc. Process for regenerating a catalyst and resultant regenerated catalyst and production of olefins by catalytic ether decomposition using regenerated catalyst
EP3064273A1 (en) * 2015-03-03 2016-09-07 Chemtura Corporation Regeneration of clay catalysts for alkylation of aromatic rings
CN105935588A (en) * 2015-03-03 2016-09-14 科聚亚公司 Regeneration of clay catalysts for alkylation of aromatic rings
US9744531B2 (en) 2015-03-03 2017-08-29 Lanxess Solutions Us Inc. Regeneration of clay catalysts for alkylation of aromatic rings

Also Published As

Publication number Publication date
BE607350A (en) 1961-12-18

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