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GB869624A - Improvements relating to resilient materials - Google Patents

Improvements relating to resilient materials

Info

Publication number
GB869624A
GB869624A GB854/58A GB85458A GB869624A GB 869624 A GB869624 A GB 869624A GB 854/58 A GB854/58 A GB 854/58A GB 85458 A GB85458 A GB 85458A GB 869624 A GB869624 A GB 869624A
Authority
GB
United Kingdom
Prior art keywords
resilient
mixture
compound
polyurethane foam
crumbed
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
GB854/58A
Inventor
Colin Thomas Gildea
Frederick Charles Jennings
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.)
Dunlop Rubber Co Ltd
Original Assignee
Dunlop Rubber Co Ltd
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 Dunlop Rubber Co Ltd filed Critical Dunlop Rubber Co Ltd
Priority to GB854/58A priority Critical patent/GB869624A/en
Priority claimed from GB21417/59A external-priority patent/GB898272A/en
Priority to FR830942A priority patent/FR1269141A/en
Publication of GB869624A publication Critical patent/GB869624A/en
Priority to GB4305/62A priority patent/GB1029961A/en
Priority to MY196258A priority patent/MY6200058A/en
Priority to MY196840A priority patent/MY6800040A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/33Agglomerating foam fragments, e.g. waste foam
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2307/00Characterised by the use of natural rubber
    • C08J2307/02Latex
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2321/00Characterised by the use of unspecified rubbers
    • C08J2321/02Latex
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes
    • C08J2375/06Polyurethanes from polyesters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes
    • C08J2375/08Polyurethanes from polyethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2475/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2475/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2475/04Polyurethanes
    • C08J2475/08Polyurethanes from polyethers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A method of making a resilient material comprises the steps of depositing or forming, on fragments of resilient cellular material, a liquid bonding agent derived from (a) an organic compound having at least two -NCX radicals in its molecule, where X represents in the case of each radical either an oxygen atom or a sulphur atom, and (b) an organic compound having a molecular weight (or at least an average molecular weight) within the range 500 to 10000 and having in each of its molecules at least two isocyanate-reactive groupings, and subsequently causing and/or allowing the liquid bonding agent to undergo conversion into a flexible solid reaction product. The fragments of resilient p material may be in the form of "crumb" and may consist of latex foam rubber, expanded rubber, resilient polyurethane foams, and resilient cellular vinyl resin (e.g. of plasticized polyvinyl chloride). The polyurethane foam can be prepared from a liquid polyester, polyesteramide, castor oil, polyglycol or a compound containing polyglycol chains attached to carbon or nitrogen, a polyisocyanate and an activating mixture with optionally a colouring agent and hair in the reaction mixture. The organic compound (a) is preferably a diisocyanate, used with or without a triisocyanate. It may be a compound in which the NCX groups are masked or blocked or one formed by reaction of the polyisocyanate with a di- or trimethylolpropane. As compound (b) there may be used a polyester, polyesteramide, polyether or polythioether, thioplast, polyamide, epoxy resin or a monomeric ester such as a glycerol ester of a hydroxy-acid or a transesterification product of a glyceride, a cross-linking compound such as glycol preferably being present. Compounds (a) and (b) may be deposited separately or as a prepolymer on the cellular material. Solidification may be effected by heating and/or the addition of catalysts, cross-linking agents such as primary diamines and glycols and/or the addition of cross-linking promoting agents such as an alcoholate, ester or alkanolamine chelate derived from titanium, vanadium, zirconium, aluminium or antimony. The mixture of particles and bonding agent can be shaped in moulds or formed into a continuous sheet on a conveyer belt. In typical examples (1) crumbed polyurethane foam is sprayed with a mixture of castor oil and a toluylene diisocyanate/trimethylolpropane reaction product and the treated crumb heated in a mould at 90 DEG C.; (3) a similar process is applied to a mixture of crumbed latex foam, resilient polyurethane foam and expanded synthetic rubber; (4) crumbed latex foam alone is employed; (5) resilient polyurethane foam is sprayed separately but concurrently with a toluylene diisocyanatetrimethylol propane reaction product and with ground-nut oil and the treated crumb is heated at 90 DEG C. to give a bonded product. Specifications 758,918, 776,012, 804,093, 804,094, 836,704, 849,774, 852,025, 857,660, 859,947 and 869,623 also are referred to.ALSO:A method of making a resilient material comprises the steps of depositing or forming, on fragments of resilient cellular material, a liquid bonding agent derived from (a) an organic compound having at least two -NCX radicals in its molecule, where X represents in the case of each radical either an oxygen atom or a sulphur atom, and (b) an organic compound having a molecular weight (or at least an average molecular weight) within the range 500 to 10,000 and having in each of its molecules at least two isocyanate-reactive groupings, and subsequently causing and/or allowing the liquid bonding agent to undergo conversion into a flexible solid reaction product. The fragments of resilient material may be in the form of "crumb" and may consist of latex foam rubber, expanded rubber, resilient polyurethane foams, and resilient cellular vinyl resin e.g. of plasticised polyvinyl chloride. The polyurethane foam can be prepared from a liquid polyester, polyesteramide, castor oil, polyglycol or a compound containing polyglycol chains attached to carbon or nitrogen, a polyisocyanate and an activating mixture with optionally a colouring agent and hair in the reaction mixture. The organic compound "(a)" is preferably a diisocyanate, used with or without a trisocyanate. It may be a compound in which the NCX groups are masked or blocked or one formed by reaction of the polisocyanate with a di- or trimethylolpropane. As compound "(b)" there may be used a polyester, polyesteramide, polyether or polythioether, thioplast, polyamide, epoxy resin or a monomeric ester such as a glycerol ester of hydroxy-acid or a transesterification product of a glyceride, a cross-linking compound such as glycol preferably being present. Compounds "(a)" and "(b)" may be deposited separately or as a prepolymer on the cellular material. Solidification may be effected by heating and/or the addition of cross-linking promoting agents such as an alcoholate, ester or alkanolamine chelate derived from titanium, vanadium, zirconium, aluminium or antimony. The mixture of particles and bonding agent can be shaped in moulds or formed into a continuous sheet on a conveyer belt. In Typical Examples (1) crumbed polyurethane foam is sprayed with a mixture of castor oil and a toluylene diisocyanate/trimethylolpropane reaction product and the treated crumb heated in a mould at 90 DEG C.; (3) a similar process is applied to a mixture of crumbed latex foam, resilient polyurethane foam and expanded synthetic rubber; (4) crumbed latex foam alone is employed; (5) resilient polyurethane foam is sprayed separately but concurrently with a toluylene diisocyanate/trimethylolpropane reaction product and with ground-nut oil and the treated crumb is heated at 90 degrees to give a bonded product. Specifications 758,918, 776,012, 804,093, 804,094, 836,704, 849,774, 852,025, 857,660, 859,947 and 869,623 are referred to.
GB854/58A 1957-01-12 1957-01-12 Improvements relating to resilient materials Expired GB869624A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
GB854/58A GB869624A (en) 1957-01-12 1957-01-12 Improvements relating to resilient materials
FR830942A FR1269141A (en) 1957-01-12 1960-06-23 Improvements in the manufacture of articles in polymer foams
GB4305/62A GB1029961A (en) 1957-01-12 1962-02-05 Improvements relating to cellular materials
MY196258A MY6200058A (en) 1957-01-12 1962-12-31 Improvements relating to resilient materials
MY196840A MY6800040A (en) 1957-01-12 1968-12-31 Improvements relating to cellular materials

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB854/58A GB869624A (en) 1957-01-12 1957-01-12 Improvements relating to resilient materials
GB21417/59A GB898272A (en) 1959-06-23 1959-06-23 Polymeric foam articles
FR830942A FR1269141A (en) 1957-01-12 1960-06-23 Improvements in the manufacture of articles in polymer foams
GB4305/62A GB1029961A (en) 1957-01-12 1962-02-05 Improvements relating to cellular materials

Publications (1)

Publication Number Publication Date
GB869624A true GB869624A (en) 1961-05-31

Family

ID=62529323

Family Applications (2)

Application Number Title Priority Date Filing Date
GB854/58A Expired GB869624A (en) 1957-01-12 1957-01-12 Improvements relating to resilient materials
GB4305/62A Expired GB1029961A (en) 1957-01-12 1962-02-05 Improvements relating to cellular materials

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB4305/62A Expired GB1029961A (en) 1957-01-12 1962-02-05 Improvements relating to cellular materials

Country Status (3)

Country Link
FR (1) FR1269141A (en)
GB (2) GB869624A (en)
MY (2) MY6200058A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1519362B1 (en) * 1964-03-12 1970-06-04 Sherwin Williams Co Aqueous coating agent dispersion
DE2506274A1 (en) * 1974-02-14 1975-08-21 Gen Foam Products SPRING, WATERPROOF MATERIAL AND METHOD FOR ITS MANUFACTURING
EP0878501A2 (en) 1997-05-16 1998-11-18 Lucyna Budny Process for recycling plastics and the use of recycled plastics as adsorption agents
WO2023141690A1 (en) * 2022-01-25 2023-08-03 Antonio Vivan Gilceu Brick made from crushed rigid polyurethane waste, combined with a binder, and manufacturing process

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4438220A (en) * 1981-06-18 1984-03-20 Wm. T. Burnett & Co., Inc. Polyurethane foam-filled foam resistant to combustion and method of producing same
GB2116572B (en) * 1982-03-05 1985-10-30 Kun Huang Chang High density flexible polyurethane foam
BE1007739A3 (en) * 1993-11-18 1995-10-10 Recticel Agglomerated polyurethane foam and method for manufacturing the same.

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1519362B1 (en) * 1964-03-12 1970-06-04 Sherwin Williams Co Aqueous coating agent dispersion
DE2506274A1 (en) * 1974-02-14 1975-08-21 Gen Foam Products SPRING, WATERPROOF MATERIAL AND METHOD FOR ITS MANUFACTURING
EP0878501A2 (en) 1997-05-16 1998-11-18 Lucyna Budny Process for recycling plastics and the use of recycled plastics as adsorption agents
WO2023141690A1 (en) * 2022-01-25 2023-08-03 Antonio Vivan Gilceu Brick made from crushed rigid polyurethane waste, combined with a binder, and manufacturing process

Also Published As

Publication number Publication date
MY6800040A (en) 1968-12-31
MY6200058A (en) 1962-12-31
GB1029961A (en) 1966-05-18
FR1269141A (en) 1961-08-11

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