GB712408A - Improvements in or relating to polyisocyanate modified polyester resins - Google Patents
Improvements in or relating to polyisocyanate modified polyester resinsInfo
- Publication number
- GB712408A GB712408A GB12288/51A GB1228851A GB712408A GB 712408 A GB712408 A GB 712408A GB 12288/51 A GB12288/51 A GB 12288/51A GB 1228851 A GB1228851 A GB 1228851A GB 712408 A GB712408 A GB 712408A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyester
- fibres
- acid
- polyisocyanate
- reacting
- 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
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
- C08J9/0085—Use of fibrous compounding ingredients
-
- 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
Abstract
A reinforced resin or resin foam is made by reacting a mixture of a polyester resin and short organic fibres containing amide groups with an organic polyisocyanate. Reaction is performed in an open vessel to produce a foam and under pressure to produce a dense foam or a solid resin. Specified fibres are nylon, wool, silk, rabbit hair and casein fibre. The fibres preferably have a length of 5 to 10 times their diameter and a length of 0.01-10.0 mm. The polyester is preferably derived by reacting (1) one or more dibasic acids, e.g. adipic, phthalic maleic, sebacic, methylenedisalicylic, tetrachlorophthalic, itaconic, oxalic or diglycolic and preferably a mixture of an aryl dibasic acid and an alkyl dibasic acid with (2) one or more aliphatic polyhydric alcohols, e.g. glycol or polyethylene glycol but preferably an alcohol containing three or more hydroxyl groups, e.g. glycerol, sorbitol, mannitol, pentaerythritol, trimethylolpropane or trimethylolethane. The polyester may also be prepared by reacting (1) a tribasic acid, e.g. tricarballylic, citric, camphorinic, aconitic or trimesic with (2) a diol, e.g. ethylene, diethylene- or propylene glycol. The length of the polyester chain may be controlled by modification with (1) a mono-basic acid, e.g. formic, acetic, propionic, butyric, valeric, caproic, enanthic, caprylic, pelargonic, capric, lauric, benzoic, lactic, sorbic or an unsaturated acid or with (2) an aldehyde e.g. formaldehyde, acetaldehyde, butyraldehyde, propionaldehyde, 2-ethylbutyraldehyde, 2-ethylhexaldehyde, glyoxal, pyruvicaldehyde, acrolein crotonaldehyde, 2-ethyl-3-propyl-acrolein, benzaldehyde or furfuraldehyde. Specified polyisocyanates are toluene di-isocyanate and methylene-bis-4-phenylisocyanate. Reaction between the polyisocyanate and polyester may be performed in presence of water, amines, alkalies, acetone or aluminium powder. In examples the polyester forming reactants are heated to 200 DEG C. whilst removing the water of reaction. The polyester is cooled to 160 DEG C. mixed with 1-400 per cent. of its weight of the fibres and cooled to room temperature. The polyisocyanate is then added and the mixture allowed to react or caused to react by gentle heating. The resulting products are cured by heating to 65-121 DEG C. over a period of hours.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US712408XA | 1951-01-27 | 1951-01-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB712408A true GB712408A (en) | 1954-07-21 |
Family
ID=22100128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12288/51A Expired GB712408A (en) | 1951-01-27 | 1951-05-25 | Improvements in or relating to polyisocyanate modified polyester resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB712408A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1005265B (en) * | 1955-12-10 | 1957-03-28 | Continental Gummi Werke Ag | Process for the production of molded articles from plastic waste on the basis of crosslinked polyester urethanes |
DE1039744B (en) * | 1955-10-24 | 1958-09-25 | Bayer Ag | Process for the production of high molecular weight plastics |
FR2341606A1 (en) * | 1976-02-19 | 1977-09-16 | Hoechst Ag | POLYURETHANE FOAMS CONTAINING FIBERS AND THEIR MANUFACTURE |
-
1951
- 1951-05-25 GB GB12288/51A patent/GB712408A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1039744B (en) * | 1955-10-24 | 1958-09-25 | Bayer Ag | Process for the production of high molecular weight plastics |
DE1005265B (en) * | 1955-12-10 | 1957-03-28 | Continental Gummi Werke Ag | Process for the production of molded articles from plastic waste on the basis of crosslinked polyester urethanes |
FR2341606A1 (en) * | 1976-02-19 | 1977-09-16 | Hoechst Ag | POLYURETHANE FOAMS CONTAINING FIBERS AND THEIR MANUFACTURE |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2277083A (en) | Composition | |
US3316139A (en) | Plastic structure containing fibrous layers and hollow glass spheres | |
US3637459A (en) | Structural panel having foam plastic core | |
US2317181A (en) | Urea-formaldehyde-triethanolamine hydrochloride condensation product | |
US2385374A (en) | Aqueous bonding composition | |
GB573932A (en) | Bonding of polymeric materials to the surface of articles | |
GB851668A (en) | Improvements in or relating to the production of polyurethanes | |
GB712408A (en) | Improvements in or relating to polyisocyanate modified polyester resins | |
GB924666A (en) | A process for forming polyurethane plastic rods or tubes by moulding or extrusion | |
US2902470A (en) | Phenol modified polyacetals | |
US2426128A (en) | Plastic compositions made with trimethylolnitromethane | |
US2404357A (en) | Coated methyl methacrylate polymer | |
US2763624A (en) | Polyester-polyisocyanate resins reinforced with fibers containing carbonamide groups | |
US2447621A (en) | Urea-formaldehyde molding composition | |
US2936293A (en) | Method of reacting monoesters of fatty acids and pentaerythritol with aromatic diisocyanates and preparing porous resins therefrom | |
GB676381A (en) | Improvements in or relating to thermoset resinous bodies | |
US2968581A (en) | Method of insolubilizing polymeric hydroxyl-bearing compounds | |
US2534102A (en) | Laminated glass interlayer | |
CN102212179A (en) | Preparation method of phenolic resin used for hand lay-up fiberglass-reinforced plastic | |
US2267316A (en) | Pressed fibrous product and process | |
US3074904A (en) | Laminate structures | |
GB802329A (en) | Novel buoyant bodies of polyurethane foam and a process for making the same | |
GB748697A (en) | Casting of polymeric materials | |
US3546172A (en) | Ethylene urea terminated phenolic resins | |
US2466744A (en) | Curing catalysts for aminoplasts |