GB1513807A - High-temperature resistant isocyanurate foams - Google Patents

High-temperature resistant isocyanurate foams

Info

Publication number
GB1513807A
GB1513807A GB42065/75A GB4206575A GB1513807A GB 1513807 A GB1513807 A GB 1513807A GB 42065/75 A GB42065/75 A GB 42065/75A GB 4206575 A GB4206575 A GB 4206575A GB 1513807 A GB1513807 A GB 1513807A
Authority
GB
United Kingdom
Prior art keywords
prepared
reaction
polyisocyanate
polyol
nco
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
GB42065/75A
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.)
BASF Corp
Original Assignee
BASF Wyandotte Corp
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 BASF Wyandotte Corp filed Critical BASF Wyandotte Corp
Publication of GB1513807A publication Critical patent/GB1513807A/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
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
    • 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
    • C08G18/161Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
    • 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
    • C08G18/20Heterocyclic amines; Salts thereof
    • C08G18/2009Heterocyclic amines; Salts thereof containing one heterocyclic ring
    • C08G18/2036Heterocyclic amines; Salts thereof containing one heterocyclic ring having at least three nitrogen atoms in the ring
    • 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
    • C08G18/5021Polyethers having heteroatoms other than oxygen having nitrogen
    • 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
    • C08G2101/00Manufacture of cellular products
    • 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
    • C08G2115/00Oligomerisation
    • 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
    • C08G2115/00Oligomerisation
    • C08G2115/02Oligomerisation to isocyanurate groups

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

1513807 Isocyanurate foams BASF WYANDOTTE CORP 14 Oct 1975 [24 Dec 1974] 42065/75 Heading C3R An isocyanurate foam is the reaction product of (a) a polyarylpolyalkylene polyisocyanate having a functionality of from 2À2 to 3À5 or an NCO -terminated prepolymer thereof (b) from 5 to 40 p.b.w. of a nitrogen-containing polyether polyol having a hydroxyl number of from 100- 900 and a nitrogen content of from 1-15% wt., (c) from 10-40 p.b.w. of a fluorocarbon blowing agent and (d) from 1-6 p.b.w. of a 1,3,5- tris(N,N - dialkylaminoalkyl) - S - hexahydrotriazine trimerization catalyst or the alkylene oxide and water adducts thereof, said parts being based on 100 p.b.w. of polyisocyanate. Preferred component (a) is a crude polyphenyl polymethylene polyisocyanate mixture having a viscosity of from 150-250 c.p.s. at 25‹ C., an NCO content of at least 31% wt. and having from 42-48% wt. of its NCO content present as a monomeric diphenylmethane diisocyanate; and is prepared by the phosgenation of anilineformaldehyde reaction products. The NCO- terminated prepolymer is prepared by reacting a stoichiometric excess of the polyaryl polyalkylene polyisocyanate with an organic compound having at least 2 reactive hydrogen atoms. Component (b) may be prepared by the reaction of an alkylene oxide with a compound selected from ammonia, alkylene polyamines, polyalkylene polyamines, primary alkylamines, primary aralkylamines and Mannich condensation products of a phenolic compound with formaldehyde and an alkanolamine. Optional ingredients include surfactants, fillers and pigments, and additional catalysts, e.g. catalysts which promote carbodiimide linkages, such as phospholene oxides, methyl alcohol, furfuryl alcohol, 2,4,6 - tris(dialkanolamino) - S - triazine and 2,4 - bis(dialkylamino) - 6 - N- (alkylhydroxyalkylamino) - )S - triazines, and urethane catalysts such as tertiary amines and metallo-organic salts. In the examples polyisocyanurate foams are prepared from the following formulations: (1) polyphenylpolymethylene isocyanate, trichlorofluoromethane, 1,3,5 - tris(dimethylaminopropyl) - hexahydrotriazine (TDH), a silicone surfactant, a polyol (OH number 530) prepared by the reaction of propylene oxide with the Mannich condensation product of HCHO, diethanolamine and a mixture of phenol and cresols, and either (a) bis(diethylamino) - N - methylhydroxyethanolamino - S triazine (DMT) and dibutyltin dilaurate (DBTL), or (b) furfuryl alcohol and either DBTL or dibutyltin diacetate; or (2) polyphenylpolymethylene - isocyanate, trichlorofluoromethane, TDH, DMT, DBTL, a silicone surfactant, and a polyol (OH number 450) prepared by the reaction of ethylene oxide with the propylene oxide adduct of ethylene diamine alone or in admixture with a polyol which is the ethylene oxide adduct of ethylene diamine.
GB42065/75A 1974-12-24 1975-10-14 High-temperature resistant isocyanurate foams Expired GB1513807A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US53609474A 1974-12-24 1974-12-24

Publications (1)

Publication Number Publication Date
GB1513807A true GB1513807A (en) 1978-06-07

Family

ID=24137117

Family Applications (1)

Application Number Title Priority Date Filing Date
GB42065/75A Expired GB1513807A (en) 1974-12-24 1975-10-14 High-temperature resistant isocyanurate foams

Country Status (10)

Country Link
JP (1) JPS5175800A (en)
AU (1) AU497306B2 (en)
BE (1) BE835625A (en)
CA (1) CA1044847A (en)
DE (1) DE2551809C3 (en)
FR (1) FR2295976A1 (en)
GB (1) GB1513807A (en)
IT (1) IT1060513B (en)
NL (1) NL7513046A (en)
ZA (1) ZA756433B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014113379A1 (en) * 2013-01-15 2014-07-24 Basf Se Rigid foam

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53145900A (en) * 1977-05-25 1978-12-19 Kohkoku Chem Ind Manufacture of urethaneemodified polyisocyanurate foam
JPS5620020A (en) * 1979-06-11 1981-02-25 Upjohn Co Polyol mixture

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014113379A1 (en) * 2013-01-15 2014-07-24 Basf Se Rigid foam
US9745408B2 (en) 2013-01-15 2017-08-29 Basf Se Rigid foam

Also Published As

Publication number Publication date
DE2551809C3 (en) 1979-09-20
FR2295976B1 (en) 1981-03-27
NL7513046A (en) 1976-06-28
AU497306B2 (en) 1978-12-07
AU8630175A (en) 1977-05-12
CA1044847A (en) 1978-12-19
IT1060513B (en) 1982-08-20
DE2551809B2 (en) 1978-08-03
JPS5175800A (en) 1976-06-30
DE2551809A1 (en) 1976-07-01
BE835625A (en) 1976-05-17
ZA756433B (en) 1977-01-26
FR2295976A1 (en) 1976-07-23

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19921014