Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
  • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
  • C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
  • C09K3/1021—Polyurethanes or derivatives thereof
• • 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
  • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
  • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
• • 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
  • C08G18/2805—Compounds having only one group containing active hydrogen
  • C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
  • C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
• • 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
  • C08G18/30—Low-molecular-weight compounds
  • C08G18/302—Water
  • C08G18/307—Atmospheric humidity
• • 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
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
  • C08G18/78—Nitrogen
  • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
  • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
  • C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
• • 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
  • C08G2190/00—Compositions for sealing or packing joints
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
  • C09K2200/06—Macromolecular organic compounds, e.g. prepolymers
  • C09K2200/0645—Macromolecular organic compounds, e.g. prepolymers obtained otherwise than by reactions involving carbon-to-carbon unsaturated bonds
  • C09K2200/065—Polyurethanes
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31547—Of polyisocyanurate
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31678—Of metal

Definitions

• This invention relates to polyurethane sealant compositions which were capable of being used without the need for a primer.
• Polyurethane sealant compositions typically comprise at least one urethane prepolymer.
• Sealants useful for bonding to non-porous substrates, such as glass were described, for example, in U.S. Patent 4,374,237 and U.S. Patent 4,687,533, both.
• U.S. Patent 4,374,237 describes a polyurethane sealant containing urethane prepolymers which have been further reacted with secondary amine compounds containing two silane groups.
• Patent 4,687,533 describes a polyurethane sealant containing urethane prepolymers which contain silane groups which have been prepared by reacting a polyisocyanate having at least three isocyanate groups with less than an equivalent amount of an alkoxysilane having a terminal group containing active hydrogen atoms reactive with isocyanate groups to form an isocyanatosilane having at least two unreacted isocyanate groups.
• the isocyanatosilane was mixed with additional polyisocyanate and the mixture was reacted with a polyol to form a polyurethane prepolymer having terminal isocyanato groups and pendant alkoxysilane groups.
• this invention was a polyurethane sealant composition
• a polyurethane sealant composition comprising
• a urethane prepolymer having an isocyanate functionality of at least 2.0 and a weight average molecular weight of at least 2,000; (2) a catalytic amount of a tin compound which catalyzes the reaction of isocyanate moieties and water or an active hydrogen containing compound; and
• the prepolymer further comprises silane functionality or the composition further comprises a compound or polymer which contains silane moieties and was compatible with the polyurethane prepolymer.
• the invention was a method for bonding glass to a substrate which comprises contacting a sealant according to the invention with glass and another substrate with the sealant disposed between the glass and substrate and thereafter allowing the sealant to cure so as to bond the glass to the substrate.
• the sealant composition of the invention was useful in bonding glass substrates to plastic, metal, fiberglass and composite substrates which may or may not be painted.
• the sealant composition gives unexpectedly high lap shear strength when no primer compositions have previously been applied to a painted plastic, metal, fiberglass or composite substrate.
• the adhesive compositions of the invention bond to acid resistant coating systems without the need for primers, achieve faster link-up in low temperature conditions and maintain adhesion when exposed to weathering conditions.
• the prepolymers used in the invention can be conventional prepolymers used in polyurethane adhesive compositions.
• the prepolymers were blended with a compound or polymer having silane functionality.
• the prepolymer contains silane functionality as well as isocyanate functionality.
• a urethane prepolymer having silane functionality may be the entire prepolymer used in the adhesive or it may be blended with a prepolymer which does not have silane functionality.
• Preferable urethane prepolymers for use in preparing the composition of the invention include any compound having an average isocyanate functionality of at least 2.0 and a molecular weight of at least 2,000.
• the average isocyanate functionality of the prepolymer was at least 2.2, and was more preferably at least 2.4.
• the isocyanate functionality was no greater than 4.0, more preferably, no greater than 3.5 and most preferably, no greater than 3.0.
• the weight average molecular weight of the prepolymer was at least 2,500, and was more preferably at least 3,000; and was preferably no greater than 40,000, even more preferably no greater than 20,000, more preferably, no greater than 15,000 and was most preferably no greater than 10,000.
• the prepolymer may be prepared by any suitable method, such as by reacting an isocyanate-reactive compound containing at least two isocyanate-reactive groups with an excess over stoichiometry of a polyisocyanate under reaction conditions sufficient to form the corresponding prepolymer.
• Suitable polyisocyanates for use in preparing the prepolymer include any aliphatic, cycloaliphatic, araliphatic, heterocyclic or aromatic polyisocyanate, or mixture thereof.
• the polyisocyanates used have an average isocyanate functionality of at least 2.0 and an equivalent weight of at least 80.
• the isocyanate functionality of the polyisocyanate was at least 2.0, more preferably at least 2.2, and was most preferably at least 2.4; and was preferably no greater than 4.0, more preferably no greater than 3.5, and was most preferably no greater than 3.0.
• the equivalent weight of the polyisocyanate was at least 100, more preferably at least 110, and was most preferably at least 120; and was preferably no greater than 300, more preferably no greater than 250, and was most preferably no greater than 200.
• polyisocyanates examples include ethylene diisocyanate, isophorone diisocyanate, bis(4-isocyanate cyclohexyl) methane, trimethyl hexamethyiene diisocyanate, 1 ,4-tetramethylene diisocyanate, 1 ,6-hexamethylene diisocyanate,
• Patent 3,492,330 polyisocyanates containing allophanate groups of the type described, for example, in British Patent 994,890, in Belgian Patent 761 ,626 and in published Dutch Patent Application No. 7,102,524, polyisocyanates containing isocyanurate groups of the type described in German Patents 1 ,022,789, 1 ,222,067 and 1 ,027,394 and in German Offenlegungsschrift 1 ,929,034 and 2,004,048, polyisocyanates containing urethane groups of the type described, for example, in Belgian Patent 752,261 or in U.S.
• Patent 3,394,164 polyisocyanates containing acrylated urea groups as described in German Patent 1 ,230,778, polyisocyanates containing biuret groups of the type described, for example, in German Patent 1 ,101 ,392, in British Patent 889,050 and in French Patent 7,017,514, polyisocyanates obtained by telomerization reactions of the type described, for example, in Belgian Patent 723,640, polyisocyanates containing ester groups of the type described, for example, in British Patents 965,474 and 1 ,072,956, in U.S.
• Preferred isocyanates were aromatic isocyanates. More preferred polyisocyanates include diphenylmethane-4,4'-diisocyanate and polymeric derivatives thereof, isophorone diisocyanate, tetramethylxylene diisocyanate, 1 ,6-hexamethylene diisocyante and polymeric derivatives thereof, bis(4-isocyanatocylohexyl)methane, and trimethyl hexamethylene diisocyanate. The most preferred isocyanate is diphenyl methane diisocyanate.
• isocyanate-reactive compound includes any organic compound having at least two isocyanate-reactive moieties, such as a compound containing an active hydrogen moiety, or an iminofunctional compound.
• an active hydrogen containing moiety refers to a moiety containing a hydrogen atom which, because of its position in the molecule, displays significant activity according to the Zerewitnoff test described by Wohler in the Journal of the American Chemical Society, Vol. 49, p. 3181 (1927).
• Illustrative of such active hydrogen moieties were -COOH, -OH, - NH 2 , -NH-, -CONH 2 , -SH, and -CONH-.
• Preferable active hydrogen containing compounds include polyols, polyamines, polymercaptans and polyacids.
• Suitable imino-functional compounds were those which have at least one terminal imino group per molecule, such as were described, for example, in U.S. Patent 4,910,279, which was hereby incorporated by reference in its entirety.
• the isocyanate-reactive compound was a polyol, and was more preferably a polyether polyol.
• Suitable polyols useful in the preparation of the prepolymers include, for example, polyether polyols, polyester polyols, poly(alkylene carbonate)polyols, hydroxyl- -containing polythioethers, polymer polyols, and mixtures thereof.
• Polyether polyols were well-known in the art and include, for example, polyoxyethylene, polyoxypropylene, polyoxybutylene, and polytetramethylene ether diols and triols which were prepared by reacting an unsubstituted or halogen- or aromatic-substituted ethylene oxide or propylene oxide with an initiator compound containing two or more active hydrogen groups such as water, ammonia, a polyalcohol, or an amine.
• an initiator compound containing two or more active hydrogen groups such as water, ammonia, a polyalcohol, or an amine.
• polyether polyols may be prepared by polymerizing alkylene oxides in the presence of an active hydrogen-containing initiator compound.
• active hydrogen-containing initiator compound Most preferred, however, were ethylene oxide-capped polyols prepared by reacting glycerin with propylene oxide, followed by reacting with ethylene oxide.
• Suitable alkylene oxides include ethylene oxide, propylene oxide, butylene oxides, styrene oxide, epichlorohydrin, epibromohydrin, and mixtures thereof.
• Suitable initiator compounds include water, ethylene glycol, propylene giycol, butanediol, hexanediol, glycerin, trimethylol propane, pentaerythritol, hexanetriol, sorbitol, sucrose, hydroquinone, resorcinol, catechol, bisphenyis, novolac resins, phosphoric acid, amines, and mixtures thereof.
• Polyester polyols were also well-known in the art and may be prepared by reacting a polycarboxylic acid or anhydride thereof with a polyhydric alcohol.
• suitable polycarboxylic acids include succinic acid, adipic acid, suberic acid, azelaic acid, sebacic acid, phthalic acid, isophthalic acid, maleic acid, trimellitic acid, phthalic acid anhydride, tetrahydrophthalic acid anhydride, hexahydrophthalic acid anhydride, tetrachlorophthalic acid anhydride, endomethylene tetrahydrophthalic acid anhydride, maleic acid anhydride, glutaric acid anhydride, fumaric acid, an mixtures thereof.
• suitable polyhydric alcohols include ethylene glycols, propane diols, butane diols, 1 ,6- hexanediol, 1 ,8-octanediol, neopentylglycol, glycerol, trimethylol propane, pentaerythritol, quinitol, mannitol, sorbitol, methyl glycoside, diethylene glycol, triethylene glycol, tetraethylene glycol, polyethylene glycols, polypropylene glycols, and mixtures thereof.
• Suitable polymer polyols include dispersions of polymers of vinyl monomers in a continuous polyol phase, particularly dispersions of styrene/acrylonitrile copolymers. Also useful were the so-called polyisocyanate polyaddition (PI PA) polyols (dispersions of polyurea-polyurethane particles in a polyol) and the polyurea dispersions in polyols (PHD polyols).
• PI PA polyisocyanate polyaddition
• PLD polyols polyureaddition copols of the vinyl type were described, for example, in U.S. Patent Nos. 4,390,645, 4,463,107, 4,148,840 and 4,574,137, all incorporated by reference.
• the isocyanate-reactive compound has a functionality of at least 1.5, more preferably at least 1.8, and was most preferably at least 2.0; and was preferably no greater than 4.0, more preferably no greater than 3.5, and was most preferably no greater than 3.0.
• the equivalent weight of the isocyanate-reactive compound was at least 200, more preferably at least 500, and was more preferably at least 1 ,000; and was preferably no greater than 5,000, more preferably no greater than 3,000, and was most preferably no greater than 2,500.
• the prepolymer may be prepared by any suitable method, such as bulk polymerization and solution polymerization.
• the reaction to prepare the prepolymer was carried out under anhydrous conditions, preferably under an inert atmosphere such as a nitrogen blanket, to prevent cross-linking of the isocyanate groups by atmospheric moisture.
• the reaction was preferably carried out at a temperature between 0°C and 150°C, more preferably between 25°C and 80°C, until the residual isocyanate content determined by titration of a sample was very close to the desired theoretical value.
• the isocyanate content in the prepolymers was preferably in the range of 0.1 percent to 10 percent, more preferably in the range of 1.5 percent to 5.0 percent and most preferably in the range of 1.8 percent to 3.0 percent.
• the prepolymer was present in the sealant composition in sufficient amount such that the sealant was capable of bonding glass to metal, plastic, fiberglass or composite substrates, preferably the substrates were painted and more preferably the substrates were painted with acid resistant paints.
• the polyurethane prepolymer was present in an amount of 30 percent by weight or greater based on the weight of the sealant, more preferably 50 percent by weight or greater and most preferably 65 percent by weight or greater.
• the polyurethane prepolymer was present in an amount of 99.8 percent by weight or less based on the weight of the sealant, more preferably 98 percent by weight or less and most preferably 85 percent by weight or less.
• the sealant was used to bond glass to substrates coated with acid resistant paints it was desirable to have a silane present in some form.
• the silane may be blended with the prepolymer.
• the silane was a silane which has an active hydrogen atom which was reactive with an isocyanate.
• such silane was a mercapto-silane or an amino-silane and more preferably was a mercapto-trialkoxy-silane or an amino-trialkoxy silane.
• the silane having, an active hydrogen atom reactive with isocyanate moieties can be reacted with the terminal isocyanate moieties of the prepolymer.
• Such reaction products were disclosed in U.S.
• the silane having a reactive hydrogen moiety reactive with an isocyanate moiety can be reacted into the backbone of the prepolymer by reacting such silane with the starting materials during the preparation of the prepolymer .
• the process for the preparation of prepolymers containing silane in the backbone was disclosed in U.S. Patent 4,625,012, relevant portions.
• Such silane having active hydrogen moieties, can be reacted with a polyisocyanate to form an adduct which was blended with the prepolymer reacted with a polyurethane prepolymer or reacted with a polyisocyanate and a compound having on average more than one moiety reactive with an isocyanate moiety.
• the adduct was a reaction product of a secondary amino- or mercapto-alkoxy silane and a polyisocyanate, the adduct having an average of at least one silane group and at least one isocyanate group per molecule (hereinafter "adduct").
• the adduct has at least 1.5 isocyanate groups and at least one silane group per molecule, and most preferably has at least two isocyanate groups and at least one silane group per molecule.
• the adduct level in the sealant compositions was preferably in the range of 0.5 percent to 20 percent, more preferably in the range of 1.0 percent to 10 percent and most preferably in the range of 2.0 percent to 7 percent.
• the adduct may be prepared by any suitable method, such as, for example, by reacting an secondary amino- or mercapto-alkoxy silane with a polyisocyanate compound.
• Suitable polyisocyanates for use in preparing the adduct include those described above as suitable for use in preparing the prepolymer, particularly including isopherone diisocyanate, polymethylene polyphenylisocyanates, and aliphatic polyisocyanates such as hexamethylene diisocyanate.
• the polyisocyanate was an aliphatic polyisocyanate and was most preferably an aliphatic polyisocyanate based on hexamethylene diisocyante with an equivalent weight of 195.
• the polyisocyanate used to prepare the isocyanate silane adduct preferably has a molecular weight of less than 2,000, more preferably less than 1 ,000.
• Suitable organofunctional silanes include amino- or mercapto-alkoxysilanes of the formula: (Ra)m
• R is a divalent organic group, preferably C alkylene, R', R", R, and Ra were hydrogen or alkyl, preferably C, 4 alkyl, m is an integer from 0 to 2.
• examples of such compounds include: N,N-bis[(3-triethoxysilyl)propyl]amine; N,N-bis[(3-tripropoxy- silyl)propyl]amine; N-(3-trimethoxysilyl)propyl-3-[N-(3-trimethoxysilyl)- propylamino]propionamide; N-(3-triethoxysilyl)propyl-3-[N-3-triethoxysilyl)-propyl- amino]propionamide; N-(3-trimethoxysilyl)propyl-3-[N-3-triethoxysilyl)- propylamino]propionamide; 3-trimethoxysilylpropyl 3-[N-(3-trimethoxysily
• the organofunctional silane was gamma-mercaptopropyl-trimethoxysilane (available as A189 from Union Carbide) or N,N'-bwas((3-trimethoxysilyl)propyl)amine.
• the silane and the polyisocyanate reactants were preferably combined so that the ratio of isocyanate groups to secondary amine or mercapto groups in the reaction mixture to prepare the adduct was at least 1.5, more preferably at least 2.0, and most preferably at least 2.5; and was preferably no greater than 6.0, more preferably no greater than 5.5, and most preferably no greater than 5.0.
• the adduct may be prepared by any suitable method, such as bulk or solution polymerization.
• the reaction between the polyisocyanate and the organofunctional silane was preferably carried out under anhydrous conditions, preferably under an inert atmosphere such as a nitrogen blanket, to prevent premature hydrolysis of the alkoxysilane groups and/or cross-linking of the isocyanate groups by atmospheric moisture.
• the polyisocyanate and alkoxysilane were preferably reacted under anhydrous conditions at a temperature between room temperature (20°C) and 80°C. Depending on the reagents, an exotherm may develop so that no external heating was required. Indeed, cooling may be necessary.
• the reaction was generally complete within two hours and may be catalyzed with a tin catalyst, suitably a tin salt such as a tin carboxylate, if desired.
• the reaction was suitably carried out in heat or in an inert liquid diluent or carrier. While any of the conventional inert organic solvents such as the benzene, toluene, xylene and other hydrocarbons or halohydrocarbons can be employed, it was preferable to use a compound having plasticizing properties, since the use of a plasticizer avoids the need for isolating the active reaction products from the reaction mixtures.
• the reactions to prepare the prepolymer and the adduct may be carried out in the presence of urethane catalysts.
• urethane catalysts include the stannous salts of carboxylic acids, such as stannous octoate, stannous oleate, stannous acetate, and stannous laurate.
• dialkyltin dicarboxylates such as dibutyltin diiaurate and dibutyltin diacetate were known in the art as urethane catalysts, as were tertiary amines and tin mercaptides.
• the reaction to prepare the prepolymer was catalyzed by stannous octoate.
• the amount of catalyst employed was generally between 0.005 and 5 percent by weight of the mixture catalyzed, depending on the nature of the isocyanate.
• the amount of silane present was that amount which enhances the adhesion of the adhesive to the painted surface without the need for a primer.
• the amount of silane present was preferably, 0.1 percent by weight or greater based on the weight of the sealant and most preferably 1.0 percent by weight or greater.
• the amount of silane used was preferably 10 percent by weight or greater or less and most preferably 2.0 percent by weight or less.
• the composition of the invention also contains an organotin catalyst which catalyzes the reaction of isocyanate moieties with water or an active hydrogen containing compound.
• organotin catalyst which catalyzes the reaction of isocyanate moieties with water or an active hydrogen containing compound.
• Such compounds were well known in the art. Included in the useful organotin compounds were alkyl tin oxides, stannous alkanoates, dialkyl tin carboxylates and tin mercaptides. Stannous alkanoates include stannous octoate.
• Alkyl tin oxides include dialkyl tin oxides, such as dibutyl tin oxide and its derivatives.
• the organotin catalyst was preferably a dialkyltin dicarboxylate or a dialkyltin dimercaptide.
• the dialkyltin dicarboxylate preferably corresponds to the formula (R 2 OC(O)) 2 -Sn-(R 3 ) 2 wherein R 2 and R 3 were independently in each occurrence a C, . .,. alkyl, preferably a C 1 3 alkyl and most preferably a methyl.
• Dialkyl tin dicarboxylates with lower total carbon atoms were preferred as they were more active catalysts in the compositions of the invention.
• the preferred dialkyl dicarboxylates include 1 ,1-dimethyltin diiaurate, 1 ,1 -dibutyltin diacetate and 1 ,1 -dimethyl dimaleate.
• the organo tin catalyst was present in an amount of 60 parts per million or greater based on the weight of the sealant, more preferably 120 parts by million or greater.
• the organo tin catalyst was present in an amount of 1.0 percent or less based on the weight of the sealant, more preferably 0.5 percent by weight or less and most preferably 0.1 percent by weight or less
• the sealant composition of the invention may also further contain a second catalyst which has good stability in the absence of atmospheric moisture, but which has a rapid cure rate in the presence of atmospheric moisture, such as a dimorpholinodialkyl ether, a di((dialkylmorpholino)alkyl) ether or a metal alkanoate, such as bismuth octoate.
• a preferred dimorpholinodialkyl ether was dimorpholinodiethyl ether.
• a preferred di((dialkylmorpholino)alkyl) ether was (di-(2-(3,5dimethylmorpholino)ethyl)ether).
• the dimorpholinodialkyl ether or di((dialkylmorpholino)alkyl) ether when employed, were preferably employed in an amount, based on the weight of the sealant, of 0.01 percent by weight or greater based on the sealant, more preferably 0.05 percent by weight or greater, even more preferably 0.1 percent by weight or greater and most preferably 0.2 percent by weight or greater and 2.0 percent by weight or less, more preferably 1.75 percent by weight or less, even more preferably 1.0 percent by weight or less and most preferably 0.4 percent by weight or less.
• the composition further comprises a stabilizing amount of an organophosphite.
• the organophosphite should be present in a sufficient amount to enhance the durability of bond of the adhesive composition to the paint surface and the glass surface durability of an automobile.
• at least one of the phosphorous atoms was bonded to an oxygen atom which was bonded to an aromatic moiety, such as a phenyl.
• at least one of the phosphorous atoms was bonded to an oxygen atom bonded to an alkyl moiety.
• at least one of the phosphorous atoms was bonded to both an aromatic moiety and an alkyl moiety through oxygen moieties.
• the organophosphites preferred for use in this invention were phosphites wherein the ligands on the phosphite comprise one ligand with at least one aliphatic moiety and one ligand with at least one aromatic moiety or comprises at least one ligand having both aromatic and aliphatic structure; that is alkaryl.
• Ligand as used herein refers to the groups bound to the oxygens bound to the phosphorous atoms of the phosphite.
• the phosphite corresponds to one of the following formulas
• R is independently in each occurrence C 6.18 alkyl, C 7.30 alkaryl or C 6.20 aryl; more preferably C 6.12 alkyl and most preferably C 912 alkyl.
• R 2 is independently in each occurrence C 6.18 alkylene, C 7.30 alkarylene; or C 6.20 arylene; more preferably C 7.30 alkarylene or C 6.20 arylene; even more preferably C 7.30 alkarylene and most preferably a divalent bisphenol structure for instance 1 ,3 propylene diphenyl or methylene diphenyl.
• alkyl means saturated straight or branched carbon chain.
• Alkylene means a divalent straight or branched saturated carbon chain.
• Aryl refers to a monovalent group comprising one or more aromatic rings such as phenyl, biphenyl or naphthyl.
• Arylene refers to a bivalent group which comprises aromatic rings such as phenylene, naphthalene or biphenylene.
• Alkaryl as used herein means an hydrocarbon group which contains both aliphatic and aromatic structural components; for example 1 ,3 propylene diphenyl or nonylphenyl.
• Alkarylene means a divalent group which has both aliphatic and aromatic structural components; that is such as 1 ,3 propylene diphenyiene or methylene diphenylene.
• organophosphites were poly(dipropyleneglycol) phenyl phosphite (available form Dover Chemical Corporation under the trademark and designation DOVERPHOS 12), tetrakis isodecyl 4,4'isopropylidene diphosphite (available form Dover Chemical Corporation under the trademark and designation DOVERPHOS 675), and phenyl diisodecyl phosphite (available form Dover Chemical Corporation under the trademark and designation DOVERPHOS 7).
• the organophosphite was present in an amount of 0.1 percent by weight or greater and more preferably 0.2 percent by weight or greater.
• the organophosphite was present in an amount of 1.0 percent by weight or less and more preferably 0.5 percent by weight or less. It has been discovered that by selection of this class of organophosphites the adhesion to certain paint surfaces was significantly enhanced.
• the one or more prepolymer and the silane containing compound, if present, were combined, preferably with fillers and additives known in the prior art for use in elastomehc compositions.
• fillers and additives known in the prior art for use in elastomehc compositions.
• physical properties such as viscosity, flow rate, sag, can be modified.
• the filler should be thoroughly dried before admixture therewith.
• Exemplary filler materials and additives include materials such as carbon black, titanium dioxide, clays, calcium carbonate, surface treated silicas, ultraviolet stabilizers, antioxidants, and the like. This list, however, was not comprehensive and was given merely as illustrative.
• the fillers were preferably present in an amount of 15 percent by weight or greater based on the amount of the sealant.
• the fillers were preferably present in an amount of 70 percent by weight or less based on the sealant, more preferably 50 percent by weight or less and even more preferably 30 percent by weight or less.
• the sealant composition also preferably contains one or more plasticizers or solvents to modify rheological properties to a desired consistency. Such materials should be free of water, inert to isocyanate groups, and compatible with the polymer.
• Such material may be added to the reaction mixtures for preparing the prepolymer or the adduct, or to the mixture for preparing the final sealant composition, but was preferably added to the reaction mixtures for preparing the prepolymer and the adduct, so that such mixtures may be more easily mixed and handled.
• Suitable plasticizers and solvents were well-known in the art and include dioctyl phthalate, dibutyl phthalate, a partially hydrogenated terpene commercially available as "HB-40", trioctyl phosphate, epoxy plasticizers, toluene-sulfamide, chloroparaffins, adipic acid esters, castor oil, xylene, 1-methyl-2-pyrolidinone and toluene.
• the amount of plasticizer used was that amount sufficient to give the desired rheological properties and disperse the components in the sealant composition.
• the plasticizer was present in an amount of 0 percent by weight or greater, more preferably 5 percent by weight or greater and most preferably 10 percent by weight or greater.
• the plasticizer was preferably present in an amount of 45 percent by weight or less and 40 percent by weight or less and most preferably 20 parts by weight or less.
• the sealant composition of this invention may be formulated by blending the components together using means well-known in the art. Generally the components were blended in a suitable mixer. Such blending was preferably conducted in an inert atmosphere and atmospheric moisture to prevent premature reaction. It may be advantageous to add any plasticizers to the reaction mixture for preparing the isocyanate containing prepolymer so that such mixture may be easily mixed and handled. Alternatively, the plasticizers can be added during blending of all the components. Once the sealant composition was formulated, it was packaged in a suitable container such that it was protected from atmospheric moisture. Contact with atmospheric moisture could result in premature cross-linking of the polyurethane prepolymer-containing isocyanate groups.
• the sealant composition of the invention was used to bond porous and nonporous substrates together.
• the sealant composition was applied to a substrate and the adhesive on the first substrate was thereafter contacted with a second substrate. Thereafter the adhesive was exposed to curing conditions.
• one substrate was glass and the other substrate is a plastic, metal, fiberglass or composite substrate which may optionally be painted. This method was especially effective for substrates painted with an acid resistant paint.
• the surfaces to which the adhesive was applied were cleaned prior to application, see for example U.S. Patents 4,525,511 , 3,707,521 and 3,779,794.
• the sealants of the invention were applied at ambient temperature in the presence of atmospheric moisture. Exposure to atmospheric moisture was sufficient to result in curing of the sealant. Curing may be further accelerated by applying heat to the curing sealant by means of convection heat, or microwave heating.
• This sealant can be formulated to be applied to a painted surface, such as an automobile window flange, without the need to put a primer on the surface of the substrate prior to application of the sealant.
• the sealant contains silane either in the form of a prepolymer or as an additive as described hereinbefore.
• the sealant can be formulated without the presence of silane.
• a primer was generally applied to the surface of the substrate, such as an automobile window flange, prior to contacting the sealant to the second substrate. Primers which may be used were well known to those skilled in the art. In the embodiment where one of the substrates was glass, the glass was preferably contacted with a primer prior to the application of the sealant.
• Examples of useful primers for painted surfaces such as automobile window flanges were BetaSeal 43530 primer available from Essex Specialty Products, Inc..
• Examples of useful primers for glass surfaces include BetaSeal 43518 primer and BetaSeal 43520A primer available from Essex Specialty Products, Inc.
• the sealants of this invention were especially effective in bonding to acid resistant points, such as, DuPonts Gen IVA coating which was an oxylic melamine silane modified coating, melamine carbarn coating, two part polyurethane coating and acid epoxy coating.
• Working time was the time period after application to a substrate wherein the adhesive was sufficiently tacky to be applied to the surface of a second substrate bond with the second substrate.
• the sealant of the invention was formulated to provide a working time of 6 minutes or greater more preferably 10 minutes or greater.
• the working time was 15 minutes or less and more preferably 12 minutes or less.
• Molecular weights as described herein were determined according to the following procedure: determined using the Waters Model 590 Gel Permeation Chromatograph. This unit was connected to a multiwavelength detector and a differential refractometer to measure the elution volume. A column of styrogel was used for the size exclusion and it can determine molecular weights from 250 to 50,000.
• the molecular weight of the prepolymer was then determined by measuring the elution volume through this column using tetrahydrofuran as the eluting solvent. The molecular weight was then calculated from a calibration curve of molecular weight vs. elution volume obtained from a polystyrene polyethylene glycol column. The quoted molecular weights were weight average molecular weights unless otherwise specified.
• the theoretical average molecular weight of the prepolymer was calculated as equal to the average isocyanate functionality times the isocyanate equivalent weight of the prepolymer.
• Functionality of the raw material was generally disclosed by the raw material supplier. It can be determined empirically by means of titrating the polyol or isocyanate to determine the average number functional group per molecule. One skilled in the art knows how to determine the functionality based on data developed by titration.
• a polyether polyurethane prepolymer was prepared by thoroughly mixing 386 grams of a polyoxypropylene diol having an average molecular weight of 2000 and 559 grams of polyoxypropylene triol having an average molecular weight of 4500, in a 2-liter resin kettle equipped with a mechanical agitator, a nitrogen inlet adapter and a thermometer. Under nitrogen purge, the mixture was heated to 50 °C. 170 grams of molten diphenylene methane 4, 4' diisocyanate were added to the mixture and the mixture thoroughly mixed. Then 0.1 gram of stannous octoate was introduced and the mixture was mixed for two hours. Finally, 484 grams of alkyl phthalate plasticizer and 16 grams of diethyl malonate were added to the mixture. The resulting prepolymer had an isocyanate content of 1.47 percent by weight.
• a moisture curable sealant composition was prepared under anhydrous conditions by first degassing under agitation the mixture of 1089 grams of the prepolymer of Example 1 , and 15 grams of N,N' bis((3-trimethoxysilyl)propyi) amine in a planetary mixer for 30 minutes. At this point, all the aminosilane was fully reacted with some isocyanate groups on the prepolymer. Then, to the above mixture, 65 grams of Desmodur N-3300 (an aliphatic polyisocyanate resin based on hexamethylene diisocyanate, supplied by Bayer USA Inc.) was charged and mixed for 10 minutes.
• Desmodur N-3300 an aliphatic polyisocyanate resin based on hexamethylene diisocyanate, supplied by Bayer USA Inc.
• DMDEE is dimorpholino diethyl ether
• NMP is n-methyl pyrollidone
• Fomrez SUL-11 A is dibutyl tin oxide.
• Fomrez UL-28 is dimethyl tin carboxylate
• Gen IVA basecoat ( ⁇ 1.0 mil.) and clearcoat ( ⁇ 1.0 mil.) were sprayed on E- coated panels and baked at 255°F oven for 27 min. Rectangle beads with size of
• 9x9x9 cm were layered on the panels three to four hours after their baking.
• the sealant beads were allowed to stay at ambient environment (21°C/30%RH) for three hours before being removed to low temperature environment (5°C/50%RH) for extended period.
• Adhesion was checked using quick knife method immediately after the indicated time.
• the cured bead was then cut with a razor blade through to the painted surface at 45 angle while pulling back the end of the bead at 180 angle. Notches were cut every 3 mm on the painted surface.
• the degree of adhesion was evaluated as adhesive failure (AF) and/or cohesive failure (CF). In case of adhesive failure, the cured bead can be separated from the painted surface, while in cohesive failure, separation occurs within the sealant bead as a result of cutting and pulling.
• AF adhesive failure
• CF cohesive failure
• Adhesion durability was tested by preparing peel samples, aging them at 110°C for the indicated time, and performing the peel adhesion test by quick knife method.
• the peel samples were prepared by applying two-step glass primer to glass coupons followed by the application of a sealant bead and pressing to obtain desired thickness (2-3 mm).
• the samples were allowed to cure at 23°C/50%RH condition for 1 week before put into 110°C oven. Samples were removed at 7, 15, 20, 24, 31 days and adhesion was tested.
• a sealant approximately 6.3 mm wide by 8 mm high was applied along the width of the glass and approximately 6 mm to 12 mm from the primed end.
• the paint substrate was immediately placed on the sealant and the sample was allowed to cure at the condition of the 23°C and 50 percent relative humidity for 7 days.
• the sample was then pulled at a rate of 1 inch/minute (2.5 cm/min)with an Instron Tester. The load at break of the sample was recorded.
• Phosphite 3 was available from Dover Chemical Corporation under the trademark and designation DOVERPHOS 49 and has the structure
• Phosphite 4 was available from Dover Chemical Company under the trademark and designation DOVERPHOS 675 and corresponds to the structure
• Phosphite 5 was available from Dover Chemical Company under the trademark and designation DOVERPHOS H-P4 and has a structure of
• Trial 1 147.2 (66.8) 0.2 (1. ) 736.0 (5070) 30%CF/30%G/40%AFP
• Trail 1 117.7 (53.4) 0.31 (2.0) 379.7 (2618) 5%CF/95%AFP
• Trail 2 137.6 (62.4) 0.33 (2.1 ) 417.0 (2875) 5%CF/95%AFP
• Trail 3 131.2 (59.5) 0.32 (2.1) 410.0 (2827) 5%CF/95%AFP
• Stabilizer 1 was available from Ciba Specialty Chemicals under the trademark and designation Tinuvin 765 and corresponds to the structure
• Stabilizer 2 was available from Ciba Specialty Chemicals under the trademark and designation Irganox 1135 and corresponds to the structure
• Stabilizer 3 was available from Dover Chemical Company under the trademark and designation Dovernox DD 9821 and was a 1 :1 blend of dinonyl phenol and a compound which corresponds to the formula Stabilizer 4 was available for Ciba Specialty Chemicals under the trademark
• Tinuvin 123 and corresponds to the formula

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• Chemical & Material Sciences (AREA)
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• Materials Engineering (AREA)
• Medicinal Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
• Polymers & Plastics (AREA)
• Polyurethanes Or Polyureas (AREA)
• Sealing Material Composition (AREA)
• Joining Of Glass To Other Materials (AREA)
• Adhesives Or Adhesive Processes (AREA)
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• 2000
  • 2000-02-04 AU AU29832/00A patent/AU2983200A/en not_active Abandoned
  • 2000-02-04 EP EP00908502A patent/EP1155093B1/en not_active Expired - Lifetime
  • 2000-02-04 JP JP2000597383A patent/JP4663881B2/ja not_active Expired - Fee Related
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  • 2000-02-04 KR KR1020017009830A patent/KR100631311B1/ko not_active Expired - Fee Related
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  • 2000-02-04 US US09/498,084 patent/US6512033B1/en not_active Expired - Lifetime
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  • 2000-02-04 DE DE60010050T patent/DE60010050T2/de not_active Expired - Lifetime
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