GB869624A - Improvements relating to resilient materials - Google Patents
Improvements relating to resilient materialsInfo
- 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
Links
- 239000012858 resilient material Substances 0.000 title abstract 4
- 229920005830 Polyurethane Foam Polymers 0.000 abstract 10
- 150000001875 compounds Chemical class 0.000 abstract 10
- 239000011496 polyurethane foam Substances 0.000 abstract 10
- 239000000203 mixture Substances 0.000 abstract 8
- 239000007767 bonding agent Substances 0.000 abstract 6
- 230000001413 cellular effect Effects 0.000 abstract 6
- 239000007795 chemical reaction product Substances 0.000 abstract 6
- 229920001821 foam rubber Polymers 0.000 abstract 6
- 239000007788 liquid Substances 0.000 abstract 6
- 150000002894 organic compounds Chemical class 0.000 abstract 6
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 abstract 5
- 239000000463 material Substances 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 4
- 239000004359 castor oil Substances 0.000 abstract 4
- 235000019438 castor oil Nutrition 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- 238000004132 cross linking Methods 0.000 abstract 4
- 229920001971 elastomer Polymers 0.000 abstract 4
- 150000002148 esters Chemical class 0.000 abstract 4
- 239000012634 fragment Substances 0.000 abstract 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 abstract 4
- 229920000728 polyester Polymers 0.000 abstract 4
- 229920006149 polyester-amide block copolymer Polymers 0.000 abstract 4
- 229920000151 polyglycol Polymers 0.000 abstract 4
- 239000010695 polyglycol Substances 0.000 abstract 4
- 239000000047 product Substances 0.000 abstract 4
- 239000005060 rubber Substances 0.000 abstract 4
- -1 thioplast Polymers 0.000 abstract 4
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 abstract 3
- 229920001228 polyisocyanate Polymers 0.000 abstract 3
- 239000005056 polyisocyanate Substances 0.000 abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 235000019483 Peanut oil Nutrition 0.000 abstract 2
- 239000004952 Polyamide Substances 0.000 abstract 2
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 abstract 2
- 230000003213 activating effect Effects 0.000 abstract 2
- 239000004411 aluminium Substances 0.000 abstract 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 abstract 2
- 229910052787 antimony Inorganic materials 0.000 abstract 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 239000013522 chelant Substances 0.000 abstract 2
- 238000004040 coloring Methods 0.000 abstract 2
- 238000000151 deposition Methods 0.000 abstract 2
- 125000005442 diisocyanate group Chemical group 0.000 abstract 2
- 239000003822 epoxy resin Substances 0.000 abstract 2
- 125000005456 glyceride group Chemical group 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 150000001261 hydroxy acids Chemical class 0.000 abstract 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- 239000000312 peanut oil Substances 0.000 abstract 2
- 229920002647 polyamide Polymers 0.000 abstract 2
- 229920000647 polyepoxide Polymers 0.000 abstract 2
- 229920000570 polyether Polymers 0.000 abstract 2
- 229920006295 polythiol Polymers 0.000 abstract 2
- 230000001737 promoting effect Effects 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 238000007711 solidification Methods 0.000 abstract 2
- 230000008023 solidification Effects 0.000 abstract 2
- 229920003051 synthetic elastomer Polymers 0.000 abstract 2
- 239000005061 synthetic rubber Substances 0.000 abstract 2
- 239000010936 titanium Substances 0.000 abstract 2
- 229910052719 titanium Inorganic materials 0.000 abstract 2
- 238000005809 transesterification reaction Methods 0.000 abstract 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052720 vanadium Inorganic materials 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- 229910052726 zirconium Inorganic materials 0.000 abstract 2
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003431 cross linking reagent Substances 0.000 abstract 1
- 150000004985 diamines Chemical class 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 229920000915 polyvinyl chloride Polymers 0.000 abstract 1
- 239000004800 polyvinyl chloride Substances 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical group C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/33—Agglomerating foam fragments, e.g. waste foam
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2307/00—Characterised by the use of natural rubber
- C08J2307/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2321/00—Characterised by the use of unspecified rubbers
- C08J2321/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/08—Polyurethanes from polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2475/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2475/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2475/04—Polyurethanes
- C08J2475/08—Polyurethanes 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.
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)
| 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)
| 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. |
-
1957
- 1957-01-12 GB GB854/58A patent/GB869624A/en not_active Expired
-
1960
- 1960-06-23 FR FR830942A patent/FR1269141A/en not_active Expired
-
1962
- 1962-02-05 GB GB4305/62A patent/GB1029961A/en not_active Expired
- 1962-12-31 MY MY196258A patent/MY6200058A/en unknown
-
1968
- 1968-12-31 MY MY196840A patent/MY6800040A/en unknown
Cited By (4)
| 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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