GB797965A - Polyisocyanate compositions and foams produced therefrom - Google Patents

Polyisocyanate compositions and foams produced therefrom

Info

Publication number
GB797965A
GB797965A GB10265/56A GB1026556A GB797965A GB 797965 A GB797965 A GB 797965A GB 10265/56 A GB10265/56 A GB 10265/56A GB 1026556 A GB1026556 A GB 1026556A GB 797965 A GB797965 A GB 797965A
Authority
GB
United Kingdom
Prior art keywords
diisocyanate
toluene
polytetramethylene
ether glycol
mols
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
GB10265/56A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and 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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB797965A publication Critical patent/GB797965A/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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4854Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
    • 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
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/18Catalysts containing secondary or tertiary amines or salts thereof
    • 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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/50Polyethers having heteroatoms other than oxygen
    • C08G18/5075Polyethers having heteroatoms other than oxygen having phosphorus
    • C08G18/5081Polyethers having heteroatoms other than oxygen having phosphorus having phosphorus bound to oxygen only
    • C08G18/5084Phosphate compounds
    • 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
    • C08G2110/00Foam properties
    • C08G2110/0008Foam properties flexible
    • 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
    • C08G2110/00Foam properties
    • C08G2110/0041Foam properties having specified density
    • 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
    • C08G2110/00Foam properties
    • C08G2110/0083Foam properties prepared using water as the sole blowing agent

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention comprises a polyisocyanate composition comprising a polytetramethyleneether polyisocyanate polymer, said polymer having at least three free isocyanate groups attached thereto, with the proviso that there be not more than three free isocyanate groups per 1400 units of molecular weight of polymer, with at least 60 per cent of the total weight of the composition being a residue obtained by removing the terminal hydrogen atoms from a polytetramethylene-ether glycol having a molecular weight of from about 750 to 7500, said composition having a ratio of the number of free isocyanate groups to the number of isocyanate-bearing molecules greater than 2. Such compositions (described as "prepolymers") are converted into cellular products on reaction with water. The compositions can be prepared by reacting a mixture of di- and triisocyanates with the polytetramethylene-ether glycol. Alternatively, a polytetramethyleneether glycol is reacted with two mols. of a diisocyanate and the product then reacted with a further mol. of diisocyanate. Another method is to form a diester by the reaction of a polytetramethylene-ether glycol with a dibasic acid containing also a hydroxyl group in the molecule and reacting the product with 3 mols. of a diisocyanate. Similarly, a polytetramethylene-ether glycol ester of phosphoric acid may be reacted with 3 mols. of a diisocyanate. Another method is to react a polytetramethylene-ether glycol with 2 mols. of a diisocyanate, 3 mols. of the resulting diisocyanate product than being reacted with a trihydroxy compound such as glycerine. A further method is to react 3 mols. of a diisocyanate with a compound produced by reacting 1 mol. of a diisocyanate with 1 mol. of polytetramethylene-ether glycol and a trihydroxy compound. Another method is to react a triol, such as glycerin, with 3 mols. of a diisocyanate and the product may then be mixed with the reaction product of 1 mol. of a tetramethylene-ether glycol and 2 mols. of a diisocyanate. The proportion of isocyanate groups per molecule can be increased by reacting 2 mols. of the polymer with 1 mol. of a compound containing two reactive hydrogens such as a diamine or a glycol. Specified polyisocyanates are toluene-2,4, m-phenylene, 4-methoxy-m-phenylene and 1,6 - hexamethylene diisocyanates, methylene bis - (4 - phenylisocyanate), toluene - 2,4,6 - triisocyanate and diphenylether - 2,4,41 - triisocyanate. In the reaction of the prepolymers with water to give a foam there are usually added catalysts such as N-methyl morpholine, diethyl ethanolamine, triethylamine, pyridine, or aqueous potassium or sodium carbonate. Further diisocyanate and dimethyl-polysiloxane, colouring materials, pigments and emulsifying agents may also be added. In examples: (1, 1A to 1F) a mixture of toluene-2,4,6-triisocyanate and toluene-2,4-diisocyanate. The prepolymer obtained is then mixed with additional toluene-2,4-diisocyanate and dimethyl siloxane and then with water and N-methylmorpholine to give a foam. Tables specify the six different proportions of reactants and molecular weights of the polyether; (1g, 1h and 1i) in a generally similar reaction, benzene - 1,3,5 - triisocyanate, diphenylether-2,4,41 - triisocyanate and triphenylmethane-4,41411-triisocyanate, respectively, replace the toluene triisocyanate; (2a to 2c) a triisocyanate compound is prepared by reacting a polytetramethylene-ether glycol with toluene-2,4-diisocyanate and is then reacted with an aqueous mixture of N-methylmorpholine and its hydrochloride; (3) a triol (glycerol or trimethylolpropane) is reacted with 3 mols. of a polytetramethylene-ether urethane ditolyl isocyanate (from the polyether and 2 mols. of toluene-2,4-diisocyanate) and the triisocyanate obtained is foamed with water, a dimethyl-siloxane and N-methylmorpholine, in some cases with the addition also of toluene diisocyanate; (4) a triol is formed by reacting a polytetramethyleneether glycol (HO-G-OH), toluene-2,4-diisocyanate and a triol R(OH)3. The product (HO-G-OOCNH-T-NHCOO-R(OH)2) is converted to a prepolymer by mixing with tetramethylene-ether glycol and toluene-2,4-diisocyanate, the product being foamed by adding water, additional-2,4-diisocyanate catalyst and silicone; (5) mixtures of toluene-2,4-diisocyanate, polytetramethylene-ether glycol and a polyol (diglycerol, triethanolamine, ditrimethylolpropane adipate, and glycerol, respectively) are reacted to give prepolymers which are then foamed as in previous examples; (6) polyesters prepared by reacting polytetramethylene-ether glycol, polybasic acid (adipic) and polyol (glycerol or trimethylolpropane) or from tartaric acid alone, are converted to prepolymer by reaction with toluene diisocyanate, and foamed by adding aqueous potassium carbonate or diethyl-ethanolamine and its hydrochloride and a silicone; (7) (a) a prepolymer obtained by reacting toluene-diisocyanate with a polytetramethylene-ether glycol/toluene diisocyanate reaction product is foamed with water and diethylethanolamine and its hydrochloride, (b) a polyester prepared by reacting phosphorus oxychloride and polytetramethylene-ether glycol is reacted with toluene-2,4-diisocyanate and the prepolymer obtained is foamed with water and the amine/amine hydrochloride of Example (6), (c) polytetramethyleneether glycol and a tetrol (from the reaction of ethylene diamine and propylene oxide) are reacted with toluene diisocyanate and the prepolymer obtained is foamed by the addition of additional diisocyanate, water and N-methylmorpholine, (d) a prepolymer from polytetramethylene-ether glycol, toluene-2,4-diisocyanate and methylene-5,51-bis (toluene-2,4-diisocyanate) is foamed by the addition of toluene-2,4-diisocyanate, water and N-methylmorpholine; (8) a polyester from glycerine, adipic acid and polytetramethylene-ether glycol is reacted with toluene-2,4-diisocyanate and the resulting prepolymer is foamed by adding water and diethylcyclohexylamine.
GB10265/56A 1955-04-29 1956-04-04 Polyisocyanate compositions and foams produced therefrom Expired GB797965A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US797965XA 1955-04-29 1955-04-29

Publications (1)

Publication Number Publication Date
GB797965A true GB797965A (en) 1958-07-09

Family

ID=22152870

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10265/56A Expired GB797965A (en) 1955-04-29 1956-04-04 Polyisocyanate compositions and foams produced therefrom

Country Status (4)

Country Link
BE (1) BE547375A (en)
DE (1) DE1065168B (en)
FR (1) FR1153165A (en)
GB (1) GB797965A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111040457A (en) * 2019-12-27 2020-04-21 田朝义 Preparation method of curing coated flame-retardant waterproof agent for plastics

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE572807A (en) * 1957-11-09
BE572728A (en) * 1957-11-09
BE581667A (en) * 1958-08-15
DE1144002B (en) * 1958-12-22 1963-02-21 Dow Chemical Co Process for the production of cellular molding compositions containing urethane groups
DE1106953B (en) * 1959-09-10 1961-05-18 Bayer Ag Process for the production of foams containing urethane groups

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111040457A (en) * 2019-12-27 2020-04-21 田朝义 Preparation method of curing coated flame-retardant waterproof agent for plastics
CN111040457B (en) * 2019-12-27 2022-05-06 广东精一塑胶实业有限公司 Preparation method of curing coated flame-retardant waterproof agent for plastics

Also Published As

Publication number Publication date
DE1065168B (en) 1959-09-10
BE547375A (en)
FR1153165A (en) 1958-03-03

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