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GB962726A - Resin compositions - Google Patents

Resin compositions

Info

Publication number
GB962726A
GB962726A GB10720/61A GB1072061A GB962726A GB 962726 A GB962726 A GB 962726A GB 10720/61 A GB10720/61 A GB 10720/61A GB 1072061 A GB1072061 A GB 1072061A GB 962726 A GB962726 A GB 962726A
Authority
GB
United Kingdom
Prior art keywords
products
compounds
water
association
phenol
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
GB10720/61A
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.)
Union Carbide Corp
Original Assignee
Union Carbide 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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB962726A publication Critical patent/GB962726A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/02Polyalkylene oxides

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)
  • Adhesives Or Adhesive Processes (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

The invention comprises association products of from 90 to 5 parts by weight of a polymeric ether compound containing at least an average of 400 non-cyclic aliphatic oxygen ether groups and from 10 to 95 parts by weight of a compound which contains at least one phenolic group. They are formed by merely contacting or mixing the components. The products may also include a polycarboxylic acid containing 0.3 to 1.7 free carboxylic acid groups per 100 molecular weight and having an average molecular weight of 600 to 2,000,000, e.g. polyacrylic acid. The association may be formed with or without condensation of the phenolic compound which may be in the form of a phenol-aldehyde condensate. Specified polyethers include polyalkylene oxides, particularly polymers and copolymers of ethylene-, propylene- and butylene oxides; condensates of alkylene oxides with other compounds, e.g. mono- and poly-hydric alcohols, phenols, carbohydrates, novolaks, polyamides, cellulose and its derivatives, etc.; polyethers which have been reacted with diisocyanates, diepoxides and other compounds giving a wide variety of end-groups. Specified phenols include substituted and unsubstituted mono-, di-, tri- and higher poly-nuclear phenols, mixtures of isomers, extracts from natural products, e.g. tanning, and novalaks and resoles. The contacting of the polyether and phenolic compound may be effected in a solvent, e.g. water for polyethylene oxide, or a non-solvent, or mixed together as a hot melt or in conventional thermoplastic equipment. When mixed in solution, precipitation of the association product may occur at a pH below 8. This may be prevented by the addition of compounds such as water-soluble ketones, monoalkyl ethers of alkylene glycols, basic alkali metal compounds, ammonia, water-soluble amines, alcohols, and other organic compounds. An aldehyde may be added to the polyether and phenol in any order and condensation effected with the aid of a catalyst. Inert additives which may be incorporated in the products include fillers, e.g. calcium carbonate, clay, mica, carbon black and wood flow; softening agents, e.g. water and alcohols; and dyes, pigments &c. Many examples are given, including for comparison, association products of (25) a phenolformaldehyde condensate and polyvinyl ether, and (26) a phenol-formaldehyde condensate and carboxymethyl cellulose. Uses: printing plates, gramophone records, gears, bearings, gaskets, washers, plugs, seal rings, pulleys, shoe soles, skis, tobacco containers, humidors, flower pots, floor tiles, pump impellers, pipes, solid rocket fuels, wood glues, films, sizing agents &c. Specifications 667,732, 818,737, 857,107, 869,113, 869,115 and 889,116 are referred to.
GB10720/61A 1960-03-25 1961-03-23 Resin compositions Expired GB962726A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US1747260A 1960-03-25 1960-03-25

Publications (1)

Publication Number Publication Date
GB962726A true GB962726A (en) 1964-07-01

Family

ID=21782774

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10720/61A Expired GB962726A (en) 1960-03-25 1961-03-23 Resin compositions

Country Status (2)

Country Link
DE (1) DE1545053B2 (en)
GB (1) GB962726A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2353284A (en) * 1998-03-05 2001-02-21 Nat Science Council Modified phenolic resins toughened by polyalkylene oxide and their preparation
WO2002050181A2 (en) * 2000-12-19 2002-06-27 Bausch & Lomb Incorporated Water-soluble blocking wax formulation

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2353284A (en) * 1998-03-05 2001-02-21 Nat Science Council Modified phenolic resins toughened by polyalkylene oxide and their preparation
GB2353284B (en) * 1998-03-05 2003-10-15 Nat Science Council Processes for preparing modified phenolic resins toughened by poly(alkylene oxide)
WO2002050181A2 (en) * 2000-12-19 2002-06-27 Bausch & Lomb Incorporated Water-soluble blocking wax formulation
WO2002050181A3 (en) * 2000-12-19 2002-09-26 Bausch & Lomb Water-soluble blocking wax formulation
US6586499B2 (en) 2000-12-19 2003-07-01 Bausch & Lomb Incorporated Water-soluble blocking wax formulation
US7101920B2 (en) 2000-12-19 2006-09-05 Bausch & Lomb Incorporated Water-soluble blocking wax formulation

Also Published As

Publication number Publication date
DE1545053B2 (en) 1976-05-13
DE1545053A1 (en) 1970-03-26

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