GB1005315A - Improved process for the oxidation of toluene and xylene - Google Patents

Improved process for the oxidation of toluene and xylene

Info

Publication number
GB1005315A
GB1005315A GB2362262A GB2362262A GB1005315A GB 1005315 A GB1005315 A GB 1005315A GB 2362262 A GB2362262 A GB 2362262A GB 2362262 A GB2362262 A GB 2362262A GB 1005315 A GB1005315 A GB 1005315A
Authority
GB
United Kingdom
Prior art keywords
cobalt
oxygen
oxidation
toluene
cobalt oxide
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
GB2362262A
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.)
SNIA Viscosa SpA
Original Assignee
SNIA Viscosa SpA
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 SNIA Viscosa SpA filed Critical SNIA Viscosa SpA
Publication of GB1005315A publication Critical patent/GB1005315A/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
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/74Iron group metals
    • B01J23/75Cobalt
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/255Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
    • C07C51/265Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting having alkyl side chains which are oxidised to carboxyl groups

Landscapes

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

Abstract

A process for the oxidation of the aliphatic side chains of toluene or xylene to the corresponding carboxylic acids with molecular oxygen or gases containing it, such as air, is carried out in the presence of a cobalt oxide catalyst insoluble in the hydrocarbon to be oxidized and remaining insoluble in the reaction mixture from the beginning to the end of the oxidation. The cobalt oxide is prepared by a dry method and is preferably subjected prior to use for the first time to a treatment with boiling water for a duration of 10-180 minutes. It contains an oxygen percentage higher than that corresponding to the formula CoO and preferably an oxygen content of 25-35%. The catalyst is preferably utilized together with an inert finely divided substance. In an example toluene is oxidized in an autoclave to benzoic acid by drawing air therethrough in the presence of cobalt oxide obtained by grinding cobalt carbonate to a fine powder and passing air at 600-700 DEG C. therethrough for about 2 1/2 hours and thereafter placing the powder in water and boiling for 1 hour and filtering. In another example, para-xylene is oxidized to a mixture of toluic and terephthalic acids. In a further example, the oxidation of toluene to benzoic acid is described in conjunction with a suitable apparatus.ALSO:A cobalt oxide of a higher oxygen content than cobalt monoxide is prepared by treating metallic cobalt, cobalt oxide or hydroxide or a salt of divalent cobalt with a volatile acid, e.g. cobalt, carbonate or nitrate, with oxygen or a gas containing molecular oxygen at 200-800 DEG C., the cobalt or cobalt compound being in the dry state and no liquid medium being present. Reference is made to cobalt oxides having oxygen contents of 25-35% by weight.
GB2362262A 1961-06-26 1962-06-19 Improved process for the oxidation of toluene and xylene Expired GB1005315A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT1167261 1961-06-26

Publications (1)

Publication Number Publication Date
GB1005315A true GB1005315A (en) 1965-09-22

Family

ID=11136793

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2362262A Expired GB1005315A (en) 1961-06-26 1962-06-19 Improved process for the oxidation of toluene and xylene

Country Status (5)

Country Link
BE (1) BE619393R (en)
DE (1) DE1468584A1 (en)
ES (1) ES278860A1 (en)
GB (1) GB1005315A (en)
NL (1) NL280020A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4965406A (en) * 1987-07-23 1990-10-23 Gadot Petrochemical Industries, Inc. Process for the manufacture of benzoic acid and salts thereof
US4990659A (en) * 1987-07-23 1991-02-05 Gadot Petrochemical Industries Ltd. Process for the manufacture of derivatives of benzoic acid
CN110590559A (en) * 2019-08-19 2019-12-20 浙江工业大学 Method for selectively preparing benzoic acid and derivatives thereof by oxidizing toluene and derivatives thereof through ball milling method
CN112121845A (en) * 2020-10-27 2020-12-25 广州大学 cobalt/N-doped nanosheet graphite phase carbon nitride composite material and preparation method and application thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4965406A (en) * 1987-07-23 1990-10-23 Gadot Petrochemical Industries, Inc. Process for the manufacture of benzoic acid and salts thereof
US4990659A (en) * 1987-07-23 1991-02-05 Gadot Petrochemical Industries Ltd. Process for the manufacture of derivatives of benzoic acid
CN110590559A (en) * 2019-08-19 2019-12-20 浙江工业大学 Method for selectively preparing benzoic acid and derivatives thereof by oxidizing toluene and derivatives thereof through ball milling method
CN112121845A (en) * 2020-10-27 2020-12-25 广州大学 cobalt/N-doped nanosheet graphite phase carbon nitride composite material and preparation method and application thereof
CN112121845B (en) * 2020-10-27 2023-04-21 广州大学 cobalt/N doped nano-sheet graphite phase carbon nitride composite material and preparation method and application thereof

Also Published As

Publication number Publication date
ES278860A1 (en) 1963-01-16
NL280020A (en)
DE1468584A1 (en) 1969-02-13
BE619393R (en) 1962-12-27

Similar Documents

Publication Publication Date Title
ES434311A1 (en) Process for preventing the formation of an emulsion when working up reaction mixtures containing butyraldehydes and cobalt
SU826944A3 (en) Catalyst for gas purification from carbon and hydrogen surfur compounds
GB1005315A (en) Improved process for the oxidation of toluene and xylene
GB1512305A (en) Process for regenerating spent oxidation catalysts containing vanadium oxide
GB1007353A (en) Process and catalysts for the production of unsaturated aliphatic carboxylic acids
GB788276A (en) A process for the purification of phthalic acids
GB793492A (en) An improved process for the preparation of terephthalic acid
ES8104178A1 (en) Process for preparing benzoic acid.
GB1399398A (en) Process for the manufacture of saturated aliphatic monocarbo xylic acids
FR2306967A1 (en) Terephthalic acid prepd by catalytic oxidn of p-xylene - giving prodt suitable for direct use in polyester
Rubinshtein et al. The reduction of CeO 2 in the ketonization of ch 3 cooh
GB1291968A (en) Process for the production of manganic carboxylates
US1856144A (en) Production of phosphoric acid
GB907926A (en) Improvements in or relating to the production of trimellitic acid and trimellitic anhydride
GB1307160A (en) Production of carboxylic acids
GB693775A (en) Method and apparatus for purifying air contaminated by acid or nitrous impurities
ES292362A1 (en) Method for preparing ketones containing a cyclohexylic nucleus
JPS57187039A (en) Activity improving method for metallic oxide catalyst containing tellurium
GB894735A (en) A process for the production of cyclohexanol and cyclohexanone
SU454768A2 (en) Catalyst for liuquid-phase oxydation of athylene into acetaldehyde
GB1152878A (en) Process for the production of Nitriles of Pyridine Carboxylic Acid-(3) and Pyridine Carboxylic Acid-(4)
SU111173A1 (en) A method for producing a catalyst from pyrolusite to accelerate the oxidation of hydrocarbons with atmospheric oxygen
GB1262018A (en) Preparation of aromatic carboxylic acids
SU25523A1 (en) The method of preparation of activated carbon
GB787937A (en) Improvements in or relating to the preparation of phthalic acids by oxidation of dialkyl benzenes