GB642827A - Processes of producing condensation products of phenols and processes of preserving rubber - Google Patents

Processes of producing condensation products of phenols and processes of preserving rubber

Info

Publication number
GB642827A
GB642827A GB18270/47A GB1827047A GB642827A GB 642827 A GB642827 A GB 642827A GB 18270/47 A GB18270/47 A GB 18270/47A GB 1827047 A GB1827047 A GB 1827047A GB 642827 A GB642827 A GB 642827A
Authority
GB
United Kingdom
Prior art keywords
phenol
methyl
rubber
pentane diol
resorcinol
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
GB18270/47A
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.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
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 Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB642827A publication Critical patent/GB642827A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Condensation products are obtained by reacting one molecular proportion of a polyhydric phenol such as hydroquinone resorcinol, and catechol, with two mols. of a polyhydric alcohol having two hydroxy groups linked to separate carbon atoms separated by one intervening carbon atom, in the presence of an acidic condensation catalyst such as aluminium chloride, zinc chloride, phosphoric acid and sulphuric acid. Suitable polyhydric alcohols are the 1 : 3- and 2 : 4-dihydroxy alkanes. The products are used as antioxidants in rubber including rubber-like copolymers of butadiene-1 : 3 with styrene or acrylic nitrile. In examples 2-methyl-2 : 4-pentane diol is condensed with: (1) hydroquinone; (2) resorcinol; (3) catechol; giving products which range from oily liquids to soft resins. The Specification as open to inspection under Sect. 91 includes also the use as the phenolic component phenol, o-chlorphenol, p-tertiary butyl phenol, p-methoxy phenol, b -naphthol, the xylenols, thymol and cravacrol. An example of the interaction of phenol with 2-methyl-2 : 4-pentane diol in the presence of zinc chloride is also included. This subject-matter does not appear in the Specification as accepted.ALSO:Condensation products are obtained by reacting 2 molecular proportions of a polyhydric phenol such as hydroquinone, resorcinol and catechol with two mols. of a polyhydric alcohol having two hydroxy groups linked to separate carbon atoms separated by one intervening carbon atom, in the presence of a condensation catalyst such as aluminium chloride, zinc chloride, phosphoric acid and sulphuric acid. Suitable polyhydric alcohols are the 1 : 3- and 2 : 4-dihydroxy alkanes. The products are used as antioxidants in rubber. In examples: (1) 2-methyl-2 : 4-pentane diol is condensed with hydroquinone in petroleum solvent in the presence of sulphuric acid giving a thick, dark amber liquid; (2) 2-methyl-2 : 4-pentane diol is condensed with resorcinol as in (1); (3) catechol is used in place of resorcinol in the process of (2). Rubber compositions containing the products as anti-oxidants are described. The Specification as open to inspection under Sect. 91 includes also the use as the phenolic component phenol, o-chlor-phenol, p-tertiary-butyl phenol, p-methoxy phenol, b -naphthol, the xylenols, thymol and carvacrol. An example of the interaction of phenol 2-methyl-2 : 4-pentane diol in the presence of zinc chloride is also included. This subject-matter does not appear in the Specification as accepted.ALSO:A method of preserving rubber comprises treating a rubber with a condensation product of one molecular proportion of a polyhydric phenol with two molecular proportions of a polyhydric alcohol having hydroxy groups linked to separate carbon atoms and separated by one intervening carbon atom produced in the presence of an acid condensation catalyst. Suitable phenols are hydroquinone resorcinol and catechol. Suitable alcohols are the 1 : 3-and 2 : 4-alkane diols. Rubbers which may be stabilized include India rubber, reclaimed rubber, balata, gutta percha and copolymers of butadiene with styrene or acrylonitrile. In examples there are described rubber compositions containing zinc oxide, lithopone, sulphur, diphenyl guanidine phthalate, benzoyl thio benzothiazole and paraffin and containing as antioxidants the condensation products of (1) hydroquinone and 2-methyl-2 : 4-pentane diol; (2) resorcinol and 2-methyl-2 : 4-pentane diol, and (3) catechol and 2-methyl-2 : 4-pentane diol. Tests are quoted to show the efficiency of the anti-oxidants. The Specification as open to inspection under Sect. 91 includes also the use as the phenolic components phenol, o-chlor-phenol, p-tertiary butyl phenol, p-methoxy-phenol, b -naphthol, the xylenols, thymol and carvacrol. An example of the interaction of phenol with 2-methyl-2 : 4-pentane diol in the presence of zinc chloride is also included. This subject-matter does not appear in the Specification as accepted.
GB18270/47A 1945-12-22 1947-07-10 Processes of producing condensation products of phenols and processes of preserving rubber Expired GB642827A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US642827XA 1945-12-22 1945-12-22

Publications (1)

Publication Number Publication Date
GB642827A true GB642827A (en) 1950-09-13

Family

ID=22054835

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18270/47A Expired GB642827A (en) 1945-12-22 1947-07-10 Processes of producing condensation products of phenols and processes of preserving rubber

Country Status (1)

Country Link
GB (1) GB642827A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0028200A1 (en) * 1979-10-29 1981-05-06 The Goodyear Tire & Rubber Company Alkylation of 2,6-di-tert.-alkylphenols with alkanediols

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0028200A1 (en) * 1979-10-29 1981-05-06 The Goodyear Tire & Rubber Company Alkylation of 2,6-di-tert.-alkylphenols with alkanediols

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