GB828718A - Stable, curable polyurethane compositions and method of making same - Google Patents

Stable, curable polyurethane compositions and method of making same

Info

Publication number
GB828718A
GB828718A GB23864/56A GB2386456A GB828718A GB 828718 A GB828718 A GB 828718A GB 23864/56 A GB23864/56 A GB 23864/56A GB 2386456 A GB2386456 A GB 2386456A GB 828718 A GB828718 A GB 828718A
Authority
GB
United Kingdom
Prior art keywords
peroxide
polyester
butyl
polyether
hydroperoxide
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
GB23864/56A
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.)
Aerojet Rocketdyne Holdings Inc
Original Assignee
General Tire and Rubber 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 General Tire and Rubber Co filed Critical General Tire and Rubber Co
Publication of GB828718A publication Critical patent/GB828718A/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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/83Chemically modified polymers
    • C08G18/86Chemically modified polymers by peroxides

Abstract

A polyurethane composition comprises a reaction product of a polyether, other than one consisting solely of isopropylene ether groups, or a polyester or a mixture of a polyether and a polyester and a polyisocyanate, the reaction product having mixed therewith as a curing agent 0.2 to 8 parts by weight for every 100 parts of the reaction product of an organic peroxide of the general formula R1-OOR, where R and R1 are organic groups of at least 3 carbon atoms and at least one of the groups R and R1 is an araliphatic group having a tertiary aliphatic carbon atom, an aliphatic carbon atom of the araliphatic group being attached to the peroxide oxygen group and being connected directly to but one oxygen atom. The amount of polyisocyanate is preferably equal to or only slightly in excess (6% to 15%) of that necessary to react with all the polyether and/or polyester. For rubbery products the molecular weight of the polyester or polyether is preferably above 1000. Rigid products are obtained when the polyethers or polyesters have molecular weights below 500 or 600 or by using a cross-linking agent such as trimethylol propane. Suitable polyethers are mixed poly-(ethylene-propylene) ether glycols, poly tri-, tetra- or penta-methylene ether glycols and polyneopentylene ether glycol. The peroxide is incorporated suitably by milling, and carbon black, synthetic wax, silicon dioxide and calcium carbonate can also be incorporated. Examples illustrate the use of di-cumyl peroxide in the curing of polyesters (polyethylenepropylene adipate) and polytetramethylene ether glycol. Comparison figures are given of the physical properties of a polyester urethane rubber (in some cases incorporating carbon black) with di-t-butyl peroxide, di-2,2-bis-(t-butyl peroxy) butane, t-butyl hydroperoxide, cumene hydroperoxide, methane hydroperoxide, t-butyl isopropyl benzene hydroperoxide, t-butyl perbenzoate, benzoyl peroxide, lauroyl peroxide, methyl ethyl ketone peroxide, cyclohexanone peroxide, methyl amyl ketone peroxide and bis-azoisobutyronitrile as curing catalysts.
GB23864/56A 1955-09-19 1956-08-02 Stable, curable polyurethane compositions and method of making same Expired GB828718A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US828718XA 1955-09-19 1955-09-19

Publications (1)

Publication Number Publication Date
GB828718A true GB828718A (en) 1960-02-24

Family

ID=22173977

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23864/56A Expired GB828718A (en) 1955-09-19 1956-08-02 Stable, curable polyurethane compositions and method of making same

Country Status (2)

Country Link
DE (1) DE1054235B (en)
GB (1) GB828718A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3130175A (en) * 1959-07-18 1964-04-21 Bayer Ag Polyurethane plastics
US3211700A (en) * 1960-09-21 1965-10-12 Us Rubber Co Polyurethane process using peroxides and catalysts
GB2167076A (en) * 1984-10-13 1986-05-21 Continental Gummi Werke Ag Method of producing polyurethane articles

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE884571C (en) * 1943-10-05 1954-01-11 Bayer Ag Process for the production of shaped masses
DE895648C (en) * 1944-03-30 1953-11-05 Bayer Ag Process for the production of high molecular weight products

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3130175A (en) * 1959-07-18 1964-04-21 Bayer Ag Polyurethane plastics
US3211700A (en) * 1960-09-21 1965-10-12 Us Rubber Co Polyurethane process using peroxides and catalysts
GB2167076A (en) * 1984-10-13 1986-05-21 Continental Gummi Werke Ag Method of producing polyurethane articles

Also Published As

Publication number Publication date
DE1054235B (en) 1959-04-02

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