EP1100838A1 - Mischungen aus sucrose- und aromatische amin-gestartete polyether-polyole und deren verwendung zur herstellung von polyurethan hartschaum - Google Patents

Mischungen aus sucrose- und aromatische amin-gestartete polyether-polyole und deren verwendung zur herstellung von polyurethan hartschaum

Info

Publication number
EP1100838A1
EP1100838A1 EP99934178A EP99934178A EP1100838A1 EP 1100838 A1 EP1100838 A1 EP 1100838A1 EP 99934178 A EP99934178 A EP 99934178A EP 99934178 A EP99934178 A EP 99934178A EP 1100838 A1 EP1100838 A1 EP 1100838A1
Authority
EP
European Patent Office
Prior art keywords
polyol
koh
gram
parts
reaction system
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.)
Withdrawn
Application number
EP99934178A
Other languages
English (en)
French (fr)
Inventor
Arthur K. Thomas
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.)
Huntsman International LLC
Original Assignee
Huntsman International LLC
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 Huntsman International LLC filed Critical Huntsman International LLC
Publication of EP1100838A1 publication Critical patent/EP1100838A1/de
Withdrawn legal-status Critical Current

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
    • C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
    • C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
    • C08J9/149—Mixtures of blowing agents covered by more than one of the groups C08J9/141 - C08J9/143
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/1808—Catalysts containing secondary or tertiary amines or salts thereof having alkylene polyamine groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/20—Heterocyclic amines; Salts thereof
    • C08G18/2009—Heterocyclic amines; Salts thereof containing one heterocyclic ring
    • C08G18/2036—Heterocyclic amines; Salts thereof containing one heterocyclic ring having at least three nitrogen atoms in the ring
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/4804—Two or more polyethers of different physical or chemical nature
    • C08G18/482—Mixtures of polyethers containing at least one polyether containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/50—Polyethers having heteroatoms other than oxygen
    • C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
    • C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
    • 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
    • C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
    • C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
    • C08J9/141—Hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00—Foam properties
    • C08G2110/0025—Foam properties rigid
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00—Foam properties
    • C08G2110/0041—Foam properties having specified density
    • C08G2110/005—< 50kg/m3
    • 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

Definitions

  • the invention relates to polyol blends and polyurethane reaction systems which include these blends, especially to sucrose based polyol blends.
  • Rigid polyurethane foams for refrigeration appliances as well as for applications such as rigid faced panels, hot water heaters, etc. desirably employ zero ozone depleting (ODP) physical blowing agents.
  • ODP ozone depleting
  • These zero ODP blowing agents include lower alkanes such as cyclopentane, isopentane and normal pentane.
  • the use of lower alkanes such as cyclopentane, isopentane and normal pentane as zero ODP blowing agents is limited because of the poor solubility of these alkanes and the difficulties in obtaining compatible non-separating blends of these alkanes in the polyols used to produce rigid polyurethane foams.
  • Aromatic amine based polyether polyols however, disadvantageously have high viscosity, which adversely affects foam flow.
  • Aliphatic amine based polyether polyols are disadvantageously autocatalytic.
  • Aromatic amine initiated polyols also are disadvantageously autocatalytic which limits adjustment of reactivity in applications which require slow reaction profiles.
  • solubilizing additives such as C 4 -C 30 polyoxyethylene polyether monols and polyester polyols to improve solubility of lower alkanes in the polyols.
  • solubilizing additives such as C 4 -C 30 polyoxyethylene polyether monols and polyester polyols, however, has disadvantages such as softening of the foam matrix.
  • the invention relates to an isocyanate reaction system having improved capacity for solubilizing hydrocarbon blowing agents that is substantially free of solubilizing additives.
  • the sucrose based polyol is present in an amount of about 60 wt. % to about 85% wt . % and the toluene diamine based polyol is present in an amount of about 40 wt. % to about 15 wt . , all amounts based on total combined weight of the sucrose based polyol and the toluene diamine based polyol.
  • the isocyanate reaction systems of the invention include a sucrose based polyether polyol and an aromatic amine based polyol.
  • the sucrose based polyol has a hydroxyl number of about 25 to about 700.
  • the aromatic amine based polyether polyol is any of diaminodiphenylmethane based polyether polyols, toluene diamine based polyols, and mixtures thereof, preferably toluene diamine based polyols.
  • the diaminodiphenylmethane based polyether polyols have a hydroxyl number of about 295 to about 325 mg KOH/gram.
  • the toluene diamine based polyols have a hydroxyl number of about 350 to about 810 mg KOH/gram, and a functionality of about 3.7 to about 4.0.
  • the hydrocarbon blowing agents may be any of cyclopentane, isopentane, n-pentane, neopentane, n-butane, cyclobutane, methylcyclobutane, isobutane, propane, cyclopropane, methylcyclopropane, n-hexane, 3-methylpentane, 2-methylpentane, cyclohexane, methylcyclopentane, n-heptane, 2-methylhexane, 3-ethylpentane, 2, 2, 3-trimethylbutane, 2,2- dimethylpentane, cycloheptane, methylcyclohexane, 2,2- dimethylbutane and 2 , 3-dimethylbutane .
  • the reaction system also can include a glycerine initiated polyether polyol having a hydroxyl value of about 53 to about 57 mg KOH/gram and a catalyst.
  • the catalyst may be any of pentamethyldiethylenetriamine, dimethyl cyclohexyl amine, 1,3, 5-tris (3- (dimethylamino) propyl) hexahydro-s-triazine, tin (II) acetate, tin (II) octanoate, tin (II) ethylhexanoate and tin (II) laurate, dibutyltin diacetate, dibutyltin dilaurate, dibutyltin maleate and dioctyltin diacetate.
  • the invention relates to an isocyanate reactive composition having improved capacity for solubilizing hydrocarbon blowing agents
  • the sucrose based polyether polyols may have a functionality of about 4.2 to 4.8, preferably about 4.5, and the toluene diamine based polyether polyol may have a functionality of about 3.7 to about 4.0, preferably about 3.9.
  • the compositions can also include a glycerine initiated polyether polyol having a hydroxyl number of about 45 to about 70 mg KOH/gram, preferably about 53-57 KOH/gram.
  • the reaction system includes about 41.0 parts of a sucrose based polyether polyol having a hydroxyl number of about 420 to about 480 mg KOH/gram, about 13.6 parts of a diaminodiphenylmethane based polyether polyol having 295 to about 325 mg KOH/gram, about 23.9 parts of a toluene diamine based polyol having a hydroxyl number of about 375 to about 405 mg KOH/gram, about 3.4 parts of a glycerine initiated polyol having a hydroxyl number of about 53 to 57 mg KOH/gram, about 1.8 parts of a silicone surfactant, about 1.2 parts of pentamethyldiethylenetriamine, about 0.5 parts 1, 3, 5-tris (3- (dimethylamino) propyl) hexahydro-s-triazine, about 1.3 parts water, and about 13.3 parts cyclopentane.
  • a sucrose based polyether polyol having a hydroxy
  • the invention in another aspect, relates to a method of producing a polyurethane foam.
  • the method entails reacting an organic polyisocyanate with a polyfunctional isocyanate- reactive composition described above in the presence of a hydrocarbon blowing agent.
  • Rubinol R 005 is a toluene diamine based polyether polyol available from Huntsman Polyurethanes . Rubinol R005 has a OH value of
  • Rubinol R180 is a sucrose based polyether polyol having about 70 wt. % sucrose and a hydroxyl value of 420-480 mg KOH/gram, and a functionality of 4.5 available from Huntsman Polyurethanes.
  • the initiator used to manufacture Rubinol R180 is predominantly sucrose by weight.
  • Rubinol R145 is a diaminodiphenylmethane based polyether polyol having a hydroxyl value of 310 mg KOH/gram available from Huntsman Polyurethanes .
  • Rubinol R144 is a diaminodiphenylmethane based polyether polyol having a hydroxyl value of 295-325 mg KOH/gram available from Huntsman Polyurethanes.
  • Rubinol R159 is a diaminodiphenylmethane based polyether polyol having a hydroxyl value of 485-515 mg KOH/gram available from Huntsman Polyurethanes .
  • Rubinol R260 is a sucrose based polyether polyol having a hydroxyl value of 295-325 mg KOH/gram and a functionality of about 4.5 available from Huntsman Polyurethanes.
  • Rubinol XR124 is a 95% pure toluene diamine based polyether polyol having a functionality of 3.9 available from Huntsman Polyurethanes. Rubinol XR124 has a OH value of 375-405 mg KOH/gram.
  • Rubinol F455 is a glycerine initiated polyether polyol available from Huntsman Polyurethanes. Rubinol F455 has a hydroxyl value of 53-57 mg KOH/gram.
  • Rubinate M is polymeric methylene diphenyl diisocyante available from Huntsman Polyurethanes .
  • Polycat 5 is pentamethyldiethylenetriamine available from Air Products and Chemicals, Inc.
  • Polycat 8 is dimethyl cyclohexyl amine from Air
  • Suprasec 5005 is polymeric methylene diphenyl diisocyante available from Huntsman Polyurethanes.
  • Tegostab B8461 is a silicone surfactant available from Goldschmidt Chemical Corporation.
  • substantially complete hydrocarbon solubility means no physical separation of the hydrocarbon or other ingredients normally used to make polyether polyol blends.
  • the polyol blends of the invention include sucrose based polyether polyol, an aromatic or aliphatic amine based polyether polyol, and a toluene diamine based polyether polyol.
  • the blends comprise predominately sucrose based polyether polyols.
  • the blends also can include blowing agents, as well as optional catalysts, chain extenders, and additives.
  • Sucrose based polyether polyols employed in the polyol blends of the invention have hydroxyl values from about 25 mg KOH/gram to about 700 mg KOH/gram, preferably about 40 mg KOH gram to about 600 mg KOH/gram, most preferably about 420 mg KOH/gram to about 480 mg KOH/gram.
  • Sucrose based polyether polyols and their method of manufacture are well known in the art. These polyether polyols may be prepared by any known process such as, for example, the process disclosed by Wutz in 1859, Ulmann' s Encyclopedia of Industrial Chemistry, Vol. A21, pp 670-674, VCH publishers Inc., (1992) and Encyclopedia of Chemical Technology, Vol. 7, pp. 257-262, published by Interscience Publishers, Inc. (1951), Le Maistre et al., "The Reaction of Sucrose with Ethylene Oxide," J. Org. Chem. , 13, pp. 782-785 (1948), or in U.S. Pat. 4,943,649; 4,380,502; and 4,230,824.
  • sucrose based polyether polyols are made from an initiator that includes sucrose reacted with one or more alkylene oxides. These alkoxylated sucrose polyols may contain alkoxylation products derived from other ingredients in the initiator mixture. In most cases, they contain alkoxylation products of lower molecular weight diols and triols such as diethylene glycol, glycerine and/or water.
  • the sucrose based polyether polyols may have a functionality of about 4.2 to 4.8, preferably about 4.5. Sucrose based polyether polyols which have a functionality of about 4.2 to about 4.8 are well known in the art.
  • sucrose based polyether polyols which may be used include but are not limited to Rubinol R180 and Rubinol 260, preferably Rubinol R180.
  • Aromatic amine based polyether polyols which may be used in the invention include those made from an aromatic amine reacted with one or more alkylene oxides.
  • Useful aromatic amine based polyether polyols include those based on diaminodiphenylmethane (" DAPDM” ) and/or toluenediamine (“TDA”) initiators.
  • DAPDM diaminodiphenylmethane
  • TDA toluenediamine
  • the alkoxylated aromatic amine polyols may contain alkoxylation products derived from other ingredients in the initiator mixture. In most cases they contain alkoxylation products of lower molecular weight diols and triols such as diethylene glycol, glycerine and/or water.
  • aromatic amine based polyether polyol may contain lower molecular weight diols and triols such as diethylene glycol, dipropylene glycol and/or glycerine.
  • Aromatic amine based polyether polyols such as TDA-based polyether polyols and diaminodiphenylmethane or polymethylene polyphenylene polyamine (DADPM) -based polyether polyols have been described as suitable isocyanate-reactive compounds for hydrocarbon blown rigid polyurethane foams (see, for example, EP 421269, WO 94/25514, EP 708127, US 5523333, US 5523332, US 5523334 and EP 617068) .
  • DADPM based polyols useful in the invention include Rubinol R 144, Rubinol R 145, and Rubinol R 159, preferably Rubinol R144.
  • TDA based polyols useful in the invention include but are not limited to Rubinol XR124 and Rubinol R 005, preferably Rubinol XR124.
  • TDA-based polyether polyols for use in the present invention generally have OH numbers in the range of about 350 to about 810, preferably about 350 to about 470 mg KOH/g, more preferably about 350 to about 430 mg KOH/g and have functionalities in the range of about 3.7 to about 4.0, preferably about 3.9.
  • the molecular weight is generally between about 280 to about 640 g/mol. TDA-based polyether polyols having this range of functionalities and OH values are well known in the art.
  • TDA-based polyether polyols which may be used in the present invention are obtained by the addition of alkylene oxides, such as ethylene oxide and/or propylene oxide to one or more of the various isomers of toluene diamine such as 2,4- , 2,6-, 2,3- and 3,4-TDA.
  • alkylene oxides such as ethylene oxide and/or propylene oxide
  • toluene diamine such as 2,4- , 2,6-, 2,3- and 3,4-TDA.
  • 2,3- and/or 3,4-TDA ortho-TDA or vicinal TDA
  • meta-TDA 2,4- and/or 2,6-TDA
  • Vicinal TDA is a pure isomer or mixture thereof, preferably containing about 20 to about 80 wt% 2,3-TDA and about 80 to about 20 wt% 3,4-TDA.
  • Other co-initiators can be used additionally in an amount up to about 60 % by weight of total initiator, preferably between about 5 and about 10 % by weight.
  • Glycerine initiated polyether polyols having a hydroxyl number of about 45 to about 70 mg KOH/gram, preferably about 53-57 KOH/gram also may be included in the isocyante reaction systems of the invention. These glycerine initiated polyether polyols are well known in the art.
  • Blowing agents which may be used in the blends of the invention include hydrocarbon blowing agents, preferably zero ODP blowing agents such as (cyclo) alkanes containing from 3 to 7 carbon atoms such as cyclopentane, isopentane, n-pentane, neopentane, n-butane, cyclobutane, methylcyclobutane, isobutane, propane, cyclopropane, methylcyclopropane, n-hexane, 3-methylpentane, 2-methylpentane, cyclohexane, methylcyclopentane, n-heptane, 2-methylhexane, 3-ethylpentane, 2, 2, 3-trimethylbutane, 2, 2-dimethylpentane, cycloheptane, methylcyclohexane, 2, 2-dimethylbutane and 2, 3-dimethylbutane.
  • Particularly preferred hydrocarbons are the C 5
  • Useful mixtures of n-pentane and isopentane include isopentane and n-pentane in a weight ratio of between about 20:80 to about 20:80.
  • Another other useful mixture is a mixture of cyclopentane and isopentane and/or n-pentane in a weight ratio cyclopentane :n/isopentane cf between about 5 to about 80 wherein the weight ratio n-pentane : isopentane is between about 20:80 to about 80:20.
  • hydrocarbon blowing agent s
  • other physical blowing agents may be used in amounts up to about 80 wt. % of the total physical blowing agents present.
  • Suitable other physical blowing agents include those well known and described in the art, for example dialkyl ethers, alkyl alkanoates, aliphatic and cycloaliphatic hydrofluorocarbons , hydrochlorofluorocarbons , chlorofluorocarbons, hydrochlorocarbons and fluorine- containing ethers, water and carbon dioxide.
  • water or other carbon dioxide-evolving compounds are used together with the physical blowing agents.
  • water is used as a chemical co-blowing agent, water is present in an amount of up to about 5%, preferably up to about 3% by weight based on the isocyanate-reactive compound.
  • the total amount of blowing agent used in the polyol blends of the invention for producing polyurethane foams can be readily determined by those skilled in the art, but typically is from about 10 to about 50, preferably about 20 to about 40 % by weight based on the total reaction system.
  • the amount of sucrose based polyol is preferably about 20 to about 80 % by weight, more preferably about 40 to about 75 % by weight, most preferably about 50 to about 62%
  • the amount of TDA-based polyether polyol is preferably about 5 to about 40 % by weight, more preferably about 10 to about 40 % by weight, most preferably about 13 to about 35 %
  • the amount of DADPM-based polyol is preferably about 4 to about 50 % by weight, more preferably about 10 to about 30% by weight, most preferably about 12 to about 20 %, all amounts by weight based on total weight of isocyanate-reactive compounds.
  • Catalysts used for producing the polyurethane rigid foams are, in particular, compounds which strongly accelerate the reaction hydroxyl groups, with the organic, modified or unmodified polyisocyanates .
  • Suitable catalyst compounds are strongly basic amines. Examples which may be mentioned are pentamethyldiethylenetriamine, dimethyl cyclohexyl amine, 1,3, 5-tris (3- (dimethylamino) propyl) hexahydro-s-triazine, amidines such as 2, 3-dimethyl-3, 4, 5, 6-tetrahydropyrimidine, tertiary amines such as triethylamine, tributylamine, dimethylbenzylamine, N-methylmorpholine, -ethylmorpholine, N- cyclohexylmorpholine, N, N, N ' , N ' -tetramethylethylenediamine, N, N,N" ,N' -tetramethylbutanediamine, N,N
  • tin(II) acetate tin (II) octanoate, tin (II) ethylhexanoate and tin (II) laurate
  • dialkyltin (IV) salts of organic carboxylic acids e.g. dibutyltin diacetate, dibutyltin dilaurate, dibutyltin maleate and dioctyltin diacetate.
  • the catalysts can be used either alone or in combination.
  • catalysts are tris (dialkylaminoalkyl) -s- hexahydrotriazines, in particular tris(N,N- dimethylaminopropyl) -s-hexahydrotriazine, tetraalkylammonium hydroxides such as tetramethylammonium hydroxide, alkali metal hydroxides such as sodium hydroxide and alkali metal alkoxides such as sodium methoxide and potassium isopropoxide, and also alkali metal salts of long-chain fatty acids having from 10 to 20 carbon atoms, with or without lateral OH groups. Preference is given to using from about 0.001 to about 5% by weight, in particular from about 0.05 to about 2% by weight, of catalyst or catalyst combination, based on the weight of the polyol blend.
  • Chain extenders and/or crosslinkers used which may be are diols and/or triols having molecular weights less than about 246, preferably from about 62 to about 174.
  • Examples are aliphatic, cycloaliphatic and/or araliphatic diols having from 2 to 14, preferably from 2 to 10 carbon atoms, such as ethylene glycol, 1, 3-propanediol, 1, 10-decanediol, o-, m-, p- dihydroxycyclohexane, diethylene glycol, dipropylene glycol and preferably 1, 4-butanediol, 1, 6-hexanediol and bis (2- hydroxyethyl) hydroquinone, triols such as 1,2,4-, 1,3,5- trihydroxycyclohexane, glycerol and trimethylolpropane, and low molecular weight hydroxyl-containing polyalkylene oxides based on ethylene and/or 1, 2-propylene oxide
  • Additives also may be included in the polyol blends.
  • These optional additives include crosslinking agents, for example low molecular weight polyols such as triethanolamine, foam-stabilizing agents or surfactants, for example siloxane- oxyalkylene copolymers, urethane catalysts, for example tin compounds such as stannous octoate or dibutyltin dilaurate or tertiary amines such as dimethylcyclohexylamine or triethylene diamine, fire retardants, for example halogenated alkyl phosphates such as tris chloropropyl phosphate, and fillers such as carbon black.
  • Other useful additives include surface- active substances, foam stabilizers, cell regulators, fillers, dyes, pigments, flameproofing agents, hydrolysis inhibitors, fungistatic and bacteriostatic substances.
  • Suitable surface-active substances are, for example, compounds which aid the homogenization of the starting materials and may also be suitable for regulating the cell structure of the plastics.
  • examples include emulsifiers such as the sodium salts of castor oil sulfates or of fatty acids, and also fatty acid salts with amines, e.g. diethylamine oleate, diethanolamine stearate, diethanolamine ricinoleate, salts of sulfonic acids, e.g.
  • alkali metal or ammonium salts of dodecylbenzenedisulfonic or dinaphthylmethanedisulfonic acid and ricinoleic acid foam stabilizers such as siloxane- oxyalkylene copolymers and other organopolysiloxanes, ethoxylated alkylphenols, ethoxylated fatty alcohols, paraffin oils, castor oil or ricinoleic esters, Turkey Red oil and peanut oil, and cell regulators such as paraffins, fatty alcohols and dimethylpolysiloxanes .
  • oligomeric acrylates having polyoxyalkylene and fluoroalkane radicals as side groups.
  • the surface-active substances are usually used in amounts of from 0 to about 2.5 parts by weight, based on 100 parts by weight of the polyol blend.
  • sucrose based polyether polyol blends of the invention include about 41% to about
  • a preferred polyether polyol blend includes about 50% Rubinol R180, about 16.6% Rubinol R144, about 29.2% Rubinol XR124 and about 4.2% Rubinol F455, all amounts based on the total weight of the blend. More preferably, the polyether blend includes Rubinol R180 in an amount of about 41 to about 43.8%, Rubinol R144 in an amount of about 10.2 to about 14.5%, Rubinol XR 124 in an amount of about 20 to about 25.1%, Rubinol F455 in an amount of up to about 3.6%, Tegostab B 8461 in an amount of about 1.8%, Polycat 5 in an amount of about 1.2%, Polycat 41 in an amount of about 0.5%, water in an amount of about 1.3%, and cyclopentane in an amount of about 13.3%, all amounts based on the weight cf the polyol blend including the cyclopentane.
  • the polyether polyol blends of the invention may also include non-sucrose based polyether polyols.
  • Non-sucrose based polyols can be included in amounts of up to about 49% based on the total weight of the polyether polyol blend.
  • Examples of non-sucrose based polyols include polyols initiated by sorbitol, glycerol, DETA, phenol formaldehyde, and mannich base.
  • the polyol blends of the invention advantageously achieve substantially complete solubility of zero ODP hydrocarbon blowing agents with substantially no solubilizing additives as required in the prior art.
  • substantially no solubilizing additives I mean that solubilizing additives may be present in an amount less than about 1% by weight of the total polyurethane formulation.
  • hydrocarbon soluble sucrose based polyol blends of the invention are prepared by mixing together in any order of addition of the individual components of the blend.
  • Examples 1-9 In examples 1-9, the components shown in Table 1 are blended. All amounts are parts by weight. The appearance of the resulting polyol blend is also shown. Table 1
  • polyurethane foam preferably a rigid polyurethane foam
  • the amounts of polyisocyanate and the polyol blends of the invention to be reacted to form a polyurethane foam, preferably a rigid polyurethane foam, depend upon the rigid polyurethane or urethane-modified polyisocyanurate foam to be produced and can be readily determined by those skilled in the art .
  • the rigid foam may be produced in the form of slabstock, molding, cavity fillings, sprayed foam, frothed foam or laminates with other materials such as hardboard, plasterboard, plastics, paper or metal .
  • the invention thus can produce polyurethane rigid foams by reacting a sucrose based polyol blend with polyisocyanate.
  • the sucrose polyol blend includes a sucrose based polyol and an amine based polyol wherein the sucrose based polyol is a predominate amount by weight of the blend.
  • the blend can include blowing agents, and also may include catalysts, additives, and, optional low molecular weight chain extenders and/or crosslinkers .
  • chain extenders, crosslinkers or mixtures thereof are included in the polyol blends for use in manufacture of polyurethane rigid foams, these are used in an amount of from 0 to about 30 % by weight, preferably from 0 to about 5 % by weight, based on the weight of the polyol compound
  • Isocyanates which may be reacted with the polyol blends of the invention to produce polyurethanes include any of those known in the art for the preparation of rigid polyurethane or urethane-modified polyisocyanurate foams, and in particular the aromatic polyisocyanates such as diphenylmethane diisocyanate in the form of its 2,4'-, 2,2'- and 4, 4 '-isomers and mixtures thereof, the mixtures of diphenylmethane diisocyanates (MDI) and oligomers thereof known in the art as "crude” or polymeric MDI (polymethylene polyphenylene polyisocyanates) having an isocyanate functionality of greater than 2, toluene diisocyanate in the form of its 2,4- and 2,6- isomers and mixtures thereof, 1, 5-naphthalene diisocyanate and 1, 4-diisocyanatobenzene.
  • aromatic polyisocyanates such as diphenylmethane di
  • organic polyisocyanates which may be mentioned include the aliphatic diisocyanates such as isophorone diisocyanate, 1, 6-diisocyanatohexane and 4,4'- diisocyanatodicyclohexylmethane .
  • Suitable organic polyisocyanates are the aliphatic, cycloaliphatic, araliphatic and preferably aromatic polyfunctional isocyanates known per se.
  • alkylene diisocyanates having from 4 to 12 carbon atoms in the alkylene radical, for example 1, 12-dodecane diisocyanate, 2-ethyltetramethylene 1, 4-diisocyanate, 2- methylpentamethylene, 1, 5-diisocyanate, tetramethylene 1,4- diisocyanate and preferably hexamethylene 1, 6-diisocyanate; cycloaliphatic diisocyanates such as cyclohexane 1,3- diisocyanate and 1, 4-diisocyanate and also any mixtures of these isomers, l-isocyanato-3, 3, 5-trimethyl-5- isocyanatomethylcyclohexane (isophorone diisocyanate), 2,4- and 2, 6-hexahydrotoluene diisocyanate and also the corresponding isomer mixtures, 4,4'-, 2,2'- and 2,4'- dicyclohexylmethane diis
  • organic diisocyanates and polyisocyanates can be used either individually or in the form of their mixture. Frequently, use is also made of modified polyfunctional isocyanates, i.e. products which are obtained by chemical reaction of organic diisocyanates and/or polyisocyanates. Examples which may be mentioned are diisocyanates and/or polyisocyanates containing ester, urea, biuret, allophanate, carbodiimide isocyanurate, uretdione and/or urethane groups.
  • organic, preferably aromatic, polyisocyanates containing urethane groups and from about 33.6 to about 15% by weight, preferably from about 31 to about 21% by weight, of NCO based on the total weight for example 4,4'- diphenylmethane diisocyanate modified with low molecular weight diols, triols, dialkylene glycols, trialkylene glycols or polyoxyalkylene glycols having molecular weights of up to about 1500, modified 4,4'- and 2, 4 ' -diphenylmethane diisocyanate mixtures, or modified raw MDI or 2,4- or 2,6- toluene diisocyanate, with examples of dialkylene or polyoxyalkylene glycols, which can be used either individually or as mixtures, being: diethylene and dipropylene glycols, polyoxyethylene, polyoxypropylene and polyoxypropylene- polyoxyethylene glycols, triols and/or tetrols.
  • NCO-containing prepolymers containing from about 25 to about 3.5% by weight, preferably from about 21 to about 14% by weight of NCO based on the total weight, prepared from the polyester-polyols and/or preferably polyether-polyols described below and 4, 4 ' -diphenylmethane diisocyanate, mixtures of 2,4'- and 4,4'- diphenylmethane diisocyanate, 2,4- and/or 2,6-toluene diisocyanates or raw MDI.
  • liquid polyisocyanates containing carbodiimide groups and/or isocyanurate rings and from 33.6 to 15% by weight, preferably from 31 to 21% by weight, of NCO, based on the total weight, e.g. based on 4,4'-, 2,4'- and/or 2, 2 ' -diphenylmethane diisocyanate and/or 2,4- and/or 2,6-toluene diisocyanate.
  • the modified polyisocyanates can, if desired, be mixed with one another or with unmodified organic polyisocyanates such as 2,4'-, 4, 4 ' -diphenylmethane diisocyanate, raw MDI, 2,4- and/or 2,6-toluene diisocyanates.
  • unmodified organic polyisocyanates such as 2,4'-, 4, 4 ' -diphenylmethane diisocyanate, raw MDI, 2,4- and/or 2,6-toluene diisocyanates.
  • Organic polyisocyanates which have been found to be particularly useful and are therefore preferably used are: mixtures of toluene diisocyanates and raw MDI or mixtures of modified organic polyisocyanates containing urethane groups and from about 33.6 to about 15% by weight of NCO, in particular those based on toluene diisocyanates, 4 , 4 ' -diphenylmethane diisocyanate, diphenylmethane diisocyanate isomer mixtures or raw MDI and, in particular, raw MDI containing from 30 to 80% by weight, preferably from about 30 to about 55% by weight, of diphenylmethane diisocyanate isomers.
  • the polyurethane rigid foams can be produced with or without use of chain extenders and/or crosslinkers.
  • chain extenders e.g. crosslinkers
  • crosslinkers e.g. crosslinkers
  • the addition of chain extenders, crosslinkers or, if desired, can be advantageous for modifying the mechanical properties, e.g. hardness.
  • the polyurethane rigid foams are advantageously produced by the one-shot method, for example by means of the high-pressure or low-pressure technique in open and/or closed molds. It is particularly advantageously to react the polyol blend with the organic polyisocyanates or modified polyisocyanates.
  • the polyurethane rigid foams produced by the process of the invention have an in-place density of from about 2.0 lb/ft 3 and a thermal conductivity of about 0.14 BTU » in » h "1 '°F»ft ⁇ 2 . They are particularly suitable as insulation material in the building and refrigeration appliance sector, for example as intermediate layer in sandwich elements or for filling housings of refrigerators and freezer chests with foam.
  • Examples 10-13 in Table 2 illustrate the use of the polyol blends of the invention in the manufacture of polyurethane foams by the well known pour in place or hand mix processes.
  • the blends of Examples 10-13 are miscible.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Polyurethanes Or Polyureas (AREA)
EP99934178A 1998-07-23 1999-07-23 Mischungen aus sucrose- und aromatische amin-gestartete polyether-polyole und deren verwendung zur herstellung von polyurethan hartschaum Withdrawn EP1100838A1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US9377698P 1998-07-23 1998-07-23
US93776P 1998-07-23
PCT/US1999/016659 WO2000005289A1 (en) 1998-07-23 1999-07-23 Blends of sucrose- and aromatic amine initiated polyether polyols and their use in rigid polyurethane foam manufacture

Publications (1)

Publication Number Publication Date
EP1100838A1 true EP1100838A1 (de) 2001-05-23

Family

ID=22240645

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99934178A Withdrawn EP1100838A1 (de) 1998-07-23 1999-07-23 Mischungen aus sucrose- und aromatische amin-gestartete polyether-polyole und deren verwendung zur herstellung von polyurethan hartschaum

Country Status (3)

Country Link
EP (1) EP1100838A1 (de)
AU (1) AU5006299A (de)
WO (1) WO2000005289A1 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101821435B1 (ko) 2010-04-21 2018-01-23 다우 글로벌 테크놀로지스 엘엘씨 발포체 절연 유닛

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4437859A1 (de) † 1994-10-22 1996-04-25 Elastogran Gmbh Verfahren zur Herstellung von Polyurethan-Hartschaumstoffen mit einer verminderten Wärmeleitfähigkeit und ihre Verwendung
KR100850995B1 (ko) * 2002-01-04 2008-08-12 주식회사 엘지이아이 경질 폴리우레탄 발포체 제조용 조성물 및 그로부터제조된 경질 폴리우레탄 발포체
DE102004048728A1 (de) * 2004-10-05 2006-04-06 Basf Ag Verfahren zur Herstellung von Polyurethan-Hartschaumstoffen
AT508870B1 (de) * 2009-09-16 2015-11-15 Alutechnik Matauschek Gmbh Isolierteil
EP3458492A4 (de) * 2016-05-20 2020-02-19 Covestro Deutschland AG Polyurethanschaum und polyurethanverbund damit
US10640600B2 (en) * 2018-04-24 2020-05-05 Covestro Llc Rigid polyurethane foams suitable for use as panel insulation
CN110229298B (zh) * 2019-06-03 2024-02-27 万华化学集团股份有限公司 一种聚脲基多元醇及制备方法和聚醚型鞋底原液及制备方法
CN114144449B (zh) * 2019-07-24 2024-05-31 陶氏环球技术有限责任公司 配制的多元醇组合物
CN112225890B (zh) * 2020-09-22 2023-05-30 万华化学（宁波）容威聚氨酯有限公司 用于低沸点低密快脱体系的氨基聚醚多元醇、制备方法和用其制备的聚氨酯硬质泡沫及方法
CN112375198B (zh) * 2020-10-28 2022-09-06 山东一诺威聚氨酯股份有限公司 低气味高性能车门内饰板组合料及其制备方法
DE102022100963A1 (de) 2022-01-17 2023-07-20 Metsä Tissue Oyj Verfahren zur Behandlung von Faserstoffen für Tissuepapier, Pulpe und Tissuepapier
CN115894888A (zh) * 2022-12-06 2023-04-04 万华化学（烟台）容威聚氨酯有限公司 一种含氟苯胺基聚醚多元醇及其制备方法和聚氨酯硬质泡沫

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4469822A (en) * 1983-07-14 1984-09-04 Basf Wyandotte Corporation Alkylene oxide adducts of vicinal toluenediamine and co-initiators, useful for rigid polyurethane foams
JP3587563B2 (ja) * 1994-08-16 2004-11-10 三井化学株式会社 硬質ポリウレタンフォーム
US5547998A (en) * 1995-11-01 1996-08-20 Basf Corporation Insulating rigid polyurethane foam compositions
DE19611367A1 (de) * 1996-03-22 1997-09-25 Bayer Ag Verfahren zur Herstellung Kohlenwasserstoff-getriebener Polyurethan-Hartschaumstoffe
BR9714225A (pt) * 1996-12-19 2000-04-18 Dow Chemical Co Uso de polióis baseados em óxido de butileno (bo) para melhorar a compatibilidade de pentano e ciclopentano em espumas de poliuretano rìgidas, produtos obtidos e processos de obtenção

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0005289A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101821435B1 (ko) 2010-04-21 2018-01-23 다우 글로벌 테크놀로지스 엘엘씨 발포체 절연 유닛

Also Published As

Publication number Publication date
WO2000005289A1 (en) 2000-02-03
AU5006299A (en) 2000-02-14

Similar Documents

Publication Publication Date Title
US5677359A (en) Three component polyol blend for use in insulating rigid polyurethane foams
US5688835A (en) Preparation of polyurethane rigid foams
JP5564055B2 (ja) 独立気泡硬質ポリウレタン発泡体の調製方法
EP3097132B1 (de) Verfahren zur herstellung von polyurethanhartschaumstoffen
EP0708127B2 (de) Verfahren zur Herstellung von Polyurethan-Hartschaumstoffen mit einer verminderten Wärmeleitfähigkeit
US7671104B2 (en) Fine cell, water-blown rigid polyurethane foams
AU722500B2 (en) Process for the production of rigid polyurethane foams having low thermal conductivity
US5684092A (en) Production of rigid foams based on isocyanate
US5523334A (en) Insulating rigid polyurethane foams
US5525641A (en) Method of making insulating rigid polyurethane foams
US5883146A (en) Dimensionally stable closed cell rigid polyisocyanate based foam prepared from a froth foaming mixture
WO2000005289A1 (en) Blends of sucrose- and aromatic amine initiated polyether polyols and their use in rigid polyurethane foam manufacture
US5523333A (en) Polyol compositions and rigid polyisocyanate based foams containing 2-chloropropane and aliphatic hydrocarbon blowing agents
EP0906354B1 (de) Verfahren zur herstellung von polyurethan-hartschaumstoffen
EP0858477B2 (de) Verfahren zur herstellung von isolierenden polyurethanhartschaumstoffen
US5670554A (en) Production of CFC-free polyurethane rigid foams having a reduced thermal conductivity and their use
JP2014511928A (ja) 硬質ポリウレタンフォームの製造方法
KR100554611B1 (ko) 열전도도가 감소된 경질 폴리우레탄 발포체의 제조 및 그의 용도
US5547998A (en) Insulating rigid polyurethane foam compositions
CA2213161A1 (en) Storage-stable, flame retardant-containing polyol component
US6063308A (en) Preparation of a homogeneous polyol component which is stable to separation
US12104006B2 (en) Polyol blends that include an isopropylidenediphenol-based polyether polyol, related compositions and foams
JP2001505941A (ja) 硬質ポリウレタンフォームにおけるペンタンとシクロペンタンの相溶性を向上させるためのブチレンオキシド（ｂｏ）をベースとするポリオールの使用
MXPA97002991A (en) Polyol mixtures of three components to use will seize rigi polyurethane foams

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20010111

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

17Q First examination report despatched

Effective date: 20011119

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20020530