ES2049952T3 - Procedimiento de produccion de fenol. - Google Patents

Procedimiento de produccion de fenol.

Info

Publication number
ES2049952T3
ES2049952T3 ES90403356T ES90403356T ES2049952T3 ES 2049952 T3 ES2049952 T3 ES 2049952T3 ES 90403356 T ES90403356 T ES 90403356T ES 90403356 T ES90403356 T ES 90403356T ES 2049952 T3 ES2049952 T3 ES 2049952T3
Authority
ES
Spain
Prior art keywords
sub
fraction containing
contact
phenol
reacted
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 - Lifetime
Application number
ES90403356T
Other languages
English (en)
Inventor
Bernard Juguin
Jean-Paul Boitiaux
Germain Martino
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.)
IFP Energies nouvelles
Original Assignee
IFP Energies nouvelles
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 IFP Energies nouvelles filed Critical IFP Energies nouvelles
Application granted granted Critical
Publication of ES2049952T3 publication Critical patent/ES2049952T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
    • C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
    • C07C39/04—Phenol
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

PROCESO DE PRODUCCION DE FENOL EN EL QUE: 1) SE HACE REACCIONAR BENCENO CON PROPANO Y ALCOHOL ISOPROPILICO AL CONTACTO CON CATALIZADOR A BASE DE UNA CEOLITA Y DESALUMINIZADA DE RELACION MOLAR SIO SUB 2 /AL SUB 2 O SUB 3 COMPRENDIDO ENTRE 8 Y 70, A CONTINUACION SE FRACCIONA EL PRODUCTO OBTENIDO EN UNA PRIMERA FRACCION QUE CONTIENE BENCENO NO CONVERTIDO, UNA SEGUNDA FRACCION QUE CONTIENE CUMENO Y UNA TERCERA FRACCION QUE CONTIENE POLISOPROPILBENZENOS, 2) SE HACE REACCIONAR DICHA TERCERA FRACCION CON BENCENO AL CONTACTO DE UN CATALIZADOR A BASE DE UNA CEOLITA Y DESALUMINIZADA DE RELACION MOLAR SIO SUB 2 /AL SUB 2 O SUB 3 COMPRENDIDA ENTRE 8 Y 70 O A BASE DE UNA MORDENITA DESALUMINIZADA DE RELACION ATOMICA SIÑAL GLOBAL COMPRENDIDA ENTRE 20 Y 60, Y SE OBTIENE CUMENO, 3) SE TRANSFORMA EL CUMENO OBTENIDO EN UNA MEZCLA DE ACETONA Y DE FENOL, 4) SE HIDROGENA AL MENOS PARCIALMENTE LA ACETONA OBTENIDA EN ALCOHOL ISOPROPILICO QUE SE RECICLA A CONTINUACION EN PARTE HACIA LA ETAPA 1.
ES90403356T 1989-12-21 1990-11-27 Procedimiento de produccion de fenol. Expired - Lifetime ES2049952T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8917162A FR2656300B1 (fr) 1989-12-21 1989-12-21 Procede de production de phenol.

Publications (1)

Publication Number Publication Date
ES2049952T3 true ES2049952T3 (es) 1994-05-01

Family

ID=9388944

Family Applications (1)

Application Number Title Priority Date Filing Date
ES90403356T Expired - Lifetime ES2049952T3 (es) 1989-12-21 1990-11-27 Procedimiento de produccion de fenol.

Country Status (9)

Country Link
US (1) US5160497A (es)
EP (1) EP0434485B1 (es)
JP (1) JP2844126B2 (es)
AU (1) AU639286B2 (es)
CA (1) CA2032985A1 (es)
DE (1) DE69005606T2 (es)
ES (1) ES2049952T3 (es)
FR (1) FR2656300B1 (es)
ZA (1) ZA909550B (es)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1313009B1 (it) * 1999-07-13 2002-05-29 Enichem Spa Processo per la rigenerazione di catalizzatori zeolitici.
DE10008924A1 (de) * 2000-02-25 2001-09-06 Phenolchemie Gmbh & Co Kg Verfahren zur Herstellung von Phenol
KR100852565B1 (ko) 2000-09-25 2008-08-18 엑손모빌 케미칼 패턴츠 인코포레이티드 페놀 생산에서 분해 유출물의 수소화 방법
JP4754058B2 (ja) * 2000-10-16 2011-08-24 三井化学株式会社 イソプロピルアルコールの製造方法
US7371910B2 (en) * 2000-10-20 2008-05-13 Lummus Technology Inc. Process for benzene alkylation and transalkylation of polyalkylated aromatics over improved zeolite beta catalyst
TWI266762B (en) * 2001-11-16 2006-11-21 Shell Int Research Process for the preparation of isopropanol
TWI301480B (en) * 2001-11-16 2008-10-01 Shell Int Research Process for the hydrogenation of acetone
WO2003074452A1 (en) * 2002-02-28 2003-09-12 Stone & Webster, Inc. Production of alkyl aromatic compounds
US7449420B2 (en) * 2003-03-21 2008-11-11 Stone & Webster Inc. Production of alkyl aromatic compounds with catalyst reactivation
US6977319B2 (en) * 2004-03-12 2005-12-20 Chevron Oronite Company Llc Alkylated aromatic compositions, zeolite catalyst compositions and processes for making the same
US7425659B2 (en) * 2006-01-31 2008-09-16 Exxonmobil Chemical Patents Inc. Alkylaromatics production
US7790936B2 (en) 2007-02-23 2010-09-07 Mitsui Chemicals, Inc. Process for preparing alkylated aromatic compound
US7498471B2 (en) * 2007-05-23 2009-03-03 Uop Llc Process for producing cumene
US7799958B2 (en) * 2007-10-04 2010-09-21 Barclays Bank Plc Process for the production of iso-propanol by liquid phase hydrogenation
WO2009063763A1 (ja) * 2007-11-13 2009-05-22 Mitsui Chemicals, Inc. アルキル化芳香族化合物の製造方法およびフェノールの製造方法
EP2110368A1 (en) 2008-04-18 2009-10-21 Total Petrochemicals France Alkylation of aromatic substrates and transalkylation process
IT1392325B1 (it) * 2008-09-11 2012-02-28 Polimeri Europa Spa Processo per l'alchilazione di benzene con isopropanolo o miscele di isopropanolo e propilene
WO2010042315A2 (en) * 2008-10-06 2010-04-15 Badger Licensing, Llc Process for producing cumene
TWI458695B (zh) * 2008-10-06 2014-11-01 Badger Licensing Llc 異丙苯的製造方法
WO2010047364A1 (ja) * 2008-10-23 2010-04-29 三井化学株式会社 アルキル化芳香族化合物の製造方法、クメンの製造方法およびフェノールの製造方法
IT1392929B1 (it) 2009-02-16 2012-04-02 Polimeri Europa Spa Processo integrato per la preparazione di etilbenzene e cumene
US9150469B2 (en) * 2009-05-18 2015-10-06 Uop Llc Aromatic alkylation process with reduced byproduct formation
US8242320B2 (en) * 2010-03-31 2012-08-14 Uop Llc Cumene production with high selectivity
CN111068775B (zh) * 2019-12-27 2022-09-27 常州大学 一种催化烃基过氧化氢分解的方法
CN111001441B (zh) * 2019-12-27 2022-09-27 常州大学 一种催化芳香化合物硝化的高酸度固体磺酸催化剂及制备方法

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3029292A (en) * 1962-04-10 Phenol purification
US2668859A (en) * 1951-01-10 1954-02-09 Rhone Poulenc Sa Process for the production of phenol and acetone
US2695324A (en) * 1952-05-16 1954-11-23 California Research Corp Hydrocarbon purification process
US3029293A (en) * 1960-08-19 1962-04-10 Hercules Powder Co Ltd Phenol purification
US3436429A (en) * 1966-11-23 1969-04-01 Skelly Oil Co Hydrogenation process
DE2112223B2 (de) * 1970-03-16 1973-12-20 Universal Oil Products Co., Des Plaines, Ill. (V.St.A.) Verfahren zur Herstellung von synthetischem Mordenit und dessen Verwendung
US4016213A (en) * 1971-05-03 1977-04-05 Allied Chemical Corporation Recovery of phenol, acetone and dimethyl phenyl carbinol from cumene oxidation product
US4083886A (en) * 1976-03-29 1978-04-11 Uop Inc. Transalkylation of alkylaromatic hydrocarbons
US4459426A (en) * 1980-04-25 1984-07-10 Union Oil Company Of California Liquid-phase alkylation and transalkylation process
US4735929A (en) * 1985-09-03 1988-04-05 Uop Inc. Catalytic composition for the isomerization of paraffinic hydrocarbons
US5017729A (en) * 1988-09-30 1991-05-21 Mitsui Petrochemical Industries, Ltd. Phenol preparation process and propylene recovery therefrom
CA2003925C (en) * 1988-11-28 1999-11-23 Shintaro Araki Preparation of cumene through alkylation of an aromatic compound and preparation of phenol through cumene

Also Published As

Publication number Publication date
ZA909550B (en) 1992-06-24
DE69005606D1 (de) 1994-02-10
DE69005606T2 (de) 1994-04-28
AU6832390A (en) 1991-06-27
US5160497A (en) 1992-11-03
FR2656300B1 (fr) 1993-06-11
CA2032985A1 (fr) 1991-06-22
AU639286B2 (en) 1993-07-22
EP0434485B1 (fr) 1993-12-29
FR2656300A1 (fr) 1991-06-28
JPH03291248A (ja) 1991-12-20
EP0434485A1 (fr) 1991-06-26
JP2844126B2 (ja) 1999-01-06

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