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    • 专利摘要:
    STRUCTURAL POLYURETHANE ADHESIVE The present invention relates to a two-component adhesive having high strength and extensibility, in which the mechanical properties are only slightly dependent on temperature, said polyurethane adhesive being suitable as a structural adhesive that is decomposed by heating , such that the adhesive bonds can be broken within a temperature range of interest. The adhesive contains a triol, a diol, an alkoxylated aromatic diol, a polyamine, a polyisocyanate, and a polyurethane polymer having isocyanate groups for certain reasons.
    公开号:BR112015003569B1
    申请号:R112015003569-8
    申请日:2013-08-20
    公开日:2020-12-08
    发明作者:Steffen Kelch；Wolfgang Roock；Florian Ittrich
    申请人:Sika Technology Ag；
    IPC主号:
    专利说明:

    Technical Field
    [1] The invention relates to the field of two-component polyurethane adhesives, in particular structural polyurethane adhesives. State of the art
    [2] Two-component polyurethane compositions based on polyols and polyisocyanates have long been used as elastic adhesives. They heal quickly after mixing and can therefore absorb and transmit forces after a short period of time.
    [3] Structural adhesives, also called construction adhesives or assembly adhesives, are used in the manufacturing industry to bond components in such a way that the adhesive bond is part of a permanently resistant construction. These adhesives are usually viscoplastic and must meet high demands in terms of processability, strength and adhesion forces.
    [4] For many bonded constructions, it is important that the adhesive has a uniform strength as far as possible, for example, a uniform modulus of elasticity as far as possible, throughout the range of its temperature of use, especially in the temperature range from about -35oC to about + 85oC, so that the mechanical behavior of the adhesive bond can be properly incorporated into the construction calculation. In particular, viscoplastic adhesives having high strength and high extensibility are desired, in which the mechanical properties are not very dependent on temperature. These adhesives must be easily processed, also usable in upper layer thicknesses of up to 10 millimeters and more, curable without problems with the final resistance at room temperature and in an accelerated heat curing process, and show excellent bonding to metallic and non-metallic substrates. metallic. In addition, there is a need for adhesives that have the properties mentioned above ePetição 870200067701, from 01/06/2020, p. 9/13 also, in the cured state, they can be easily separated again from the substrate to which they adhere to a specific treatment, without the substrate being damaged by this treatment, that is, the connection connection can be separated without damaging the connected components. Disclosure of the Invention
    [5] The object of the present invention is, therefore, to provide a polyurethane adhesive with high strength and high extensibility, in which the mechanical properties are not very dependent on temperature and which is therefore excellently suitable as a structural adhesive, and which can be separated again from the substrate to which it adheres in the cured state in a way that does not damage the substrate.
    [6] A polyurethane adhesive according to claim 1 has been found to achieve this goal. Due to its special composition, the adhesive has good processability, as well as high stability after mixing the components, good initial adhesive resistance, fast and problem-free curing and very high resistance in the cured state, without losing its extensibility and elasticity.
    [7] The obtained combination of strength and elongation over a range of application from -35 ° C to 85 ° C is related to greater resistance to the impact of cured material.
    [8] Particularly surprising in this context is the fact that the adhesive bonds comprising the polyurethane adhesive can be separated again by heating to a temperature of at least 120 ° C, in particular at a temperature in the range of 140 ° C to 200 ° C for at least 10 minutes, in particular at least 20 minutes, that is, the adhesive can be separated from the substrate. The temperature range in which the shutdown occurs is very advantageous. It is well above the usage temperature of many adhesive bonds, and it is still so low that many substrates of interest or bonded components do not have their function damaged by the shutdown process. This advantageous behavior is obtained, at least partially, by the alkoxylated aromatic diol.
    [9] It has also been found that the use of polyurethane adhesive, according to the invention, achieves particularly good adhesion to metal surfaces and non-metallic materials, in particular fiber-reinforced composites, such as glass-fiber-reinforced plastics and carbon fiber-reinforced plastic materials.
    [10] Other aspects of the invention are the subject of subsequent independent claims. Particularly preferred embodiments of the invention are the subject of the dependent claims. Ways of carrying out the invention
    [11] The invention relates to a polyurethane adhesive composed of a first and a second component, where - the first component contains a) at least one triol A1 having a molecular weight in the range of 1,000 to 10,000 g / mol, b) at least one A2 diol having two primary hydroxyl groups and a molecular weight in the range 60 to 150 g / mol, and c) at least one alkoxylated aromatic diolA3 having a molecular weight in the range 300 to 1,000 g / mol, and d) at least one aliphatic polyamine A4 having a molecular weight in the range of 60 to 500 g / mol; and - the second component contains e) at least one polyisocyanate B1 and f) at least one polyurethane polymer B2 having isocyanate groups; - in which triol A1, diol A2 and alkoxylated aromatic diol A3 are present in an amount such that g) the weight ratio A1 / (A2 + A3) <10, and h) the weight ratio A1 / A2 <15.
    [12] In this document, the prefix "poly" in substance names, such as "polyol", "polyisocyanate", "polyether" or "polyamine" indicates that the respective substance formally contains, per molecule, more than one functional group occurring in its name.
    [13] In this document, "molecular weight" in the case of polymers always refers to the average molecular weight.
    [14] A "primary hydroxyl group" denotes an OH group that is attached to a carbon atom with two hydrogens.
    [15] In this document, the term "phase separation" describes the process of segregating highly ordered ("crystalline") regions, also called "hard segments" and poorly ordered regions ("amorphous"), also called "segments "during the curing of the polyurethane adhesive.
    [16] In this document, "opening time" refers to the time within which the parts to be connected must be joined after the components have been mixed.
    [17] In this document, the term "strength" refers to the strength of the cured adhesive, where strength in particular should be understood to mean tensile strength and the modulus of elasticity (Young's modulus) in the elongation range of to 10%.
    [18] In this document, "adhesive bond" refers to a fixed bond of at least two substrates composed of the same or different materials by means of an adhesive.
    [19] In this document, "disconnection" of an adhesive connection refers to the deliberate weakening of the adhesive in relation to its strength. This allows the mechanical separation of the substrates with relatively little force expenditure, that is, the adhesive bond is easily separable. The separation can be done either adhesively between the adhesive and a surface of the substrate or cohesively in the adhesive.
    [20] In this document, "room temperature" refers to a temperature of 23 ° C.
    [21] The term "stable storage" refers to the property of a composition of being storable in a suitable container for several weeks to several months at room temperature, without significantly altering its application or use properties due to storage.
    [22] Suitable A1 triols are, in particular, polyoxyalkylene triols, also called polyether triols. These are the products of the polymerization of ethylene oxide, 1,2-propylene oxide, 1,2- or 2,3-butylene oxide or mixtures thereof. Typically, they are polymerized using a starting molecule having three active hydrogen atoms, such as glycerol, 1,1,1-trimethylolethane, 1,1,1-trimethylpropane or mixtures thereof.
    [23] Preferred A1 triols are polyoxypropylene triols, polyoxyethylene triols and polyoxypropylene-polyoxyethylene triols.
    [24] Particularly preferred, triol A1 has primary hydroxyl groups. In this way, the polyurethane adhesive is less susceptible to unwanted reactions by the isocyanate groups with potentially present water, which can lead to the formation of bubbles and incomplete cure.
    [25] Particularly preferred triols A1 are so called "EO-coated" polyoxypropylene triols (ethylene oxide-coated end). The latter are special polyoxypropylene-polyoxyethylene triols which are obtained, for example, by the subsequent alkoxylation of polyoxypropylene triols with ethylene oxide after the completion of the polypropoxylation and therefore have primary hydroxyl groups. In comparison to pure polyoxyethylene triols, they have the advantage that they are less hydrophilic and that they are liquid at room temperature.
    [26] Preferably, the A1 triol has an average OH functionality in the range of 2.2 to 3. Using these A1 triols, adhesives with good mechanical properties are obtained.
    [27] Preferably, the triol A1 has a molecular weight in the range of 3,000 to 8,000 g / mol, particularly preferably 4,000 to 6,000 g / mol. This triol exhibits a good combination of high functionality and chain length, so that an adhesive with good mechanical properties is obtained.
    [28] A1 triol is preferably used in an amount of 30 to 70% by weight, based on the total weight of the first component.
    [29] Suitable diols A2 are, in particular, 1,2-ethanediol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,3-cyclohexanedimethanol, 1, 4-cyclohexanedimethanol and diethylene glycol. These diols have primary hydroxyl groups that are not sterically hindered and are particularly reactive with isocyanate groups.
    [30] Preferably, the diol A2 is a linear diol, in particular, selected from the group consisting of 1,3-propanediol, 1,4-butanediol and 1,5-pentanediol. These diols are particularly easy to handle since they are not hydrophilic and are liquid at room temperature and produce urethane groups during curing of the adhesive, which favors high strength and good extensibility over a wide temperature range. Of these, 1,4-butanediol is the most preferred.
    [31] Alkoxylated aromatic diol A3 is a polyether diol having an aromatic core, since it is obtainable, in particular, by the alkoxylation of an aromatic diol having two phenolic OH groups.
    [32] The alkoxylated aromatic diol A3 is preferably an ethoxylated and / or propoxylated and / or butoxylated aromatic diol, in particular an ethoxylated and / or propoxylated aromatic diol. These diols are particularly easily accessible.
    [33] Particularly preferably, the alkoxylated aromatic diol A3 is a propoxylated aromatic diol. These diols are hydrophobic and have a very low viscosity, whereby easily processed adhesives are obtained with good resistance to moisture in the cured state.
    [34] The aromatic fraction of the alkoxylated aromatic diol A3 is preferably a benzene radical, diphenylmethane radical, 1,1-diphenylpropane radical, 2,2-diphenylpropane radical, diphenylether radical, benzophenone radical, bis (phenyl) sulfone radical or biphenyl radical.
    [35] Of these, the diphenylmethane radical and the 2,2-diphenylpropane radical are preferred. These aromatic radicals are derived from bisphenol F or bisphenol A. These alkoxylated aromatic diols A3 produce easily processable adhesives having particularly high strengths.
    [36] Particularly preferably, the alkoxylated aromatic diol A3 is a propoxylated bisphenol A or a propoxylated bisphenol F, in particular, a propoxylated bisphenol A.
    [37] The alkoxylated aromatic diol A3 preferably has a molecular weight in the range of 350 to 500 g / mol. These A3 diols produce particularly high resistances.
    [38] Suitable as A4 aliphatic polyamines are amines with two or three aliphatic groups, in particular the following commercially available polyamines: - primary aliphatic, cycloaliphatic or arylaliphatic diamines, such as, in particular, ethylenediamine, 1,2-propanediamine , 1,3-propanediamine, 2-methyl-1,2-propanediamine, 2,2-dimethyl-1,3-propanediamine, 1,3-butanediamine, 1,4-butanediamine, 1,3-pentanediamine (DAMP), 1,5-pentanediamine, 1,5-diamino-2-methylpentane (MPMD), 2-butyl-2-ethyl-1,5-pentanediamine (C11-neodynamine), 1,6-hexanediamine, 2,5-dimethyl- 1,6-hexanediamine, 2,2,4- and 2,4,4-trimethyl hexamethylene diamine (TMD), 1,7-heptanediamine, 1,8-octanediamine, 1,9-nonanediamine, 1,10-decanediamine, 1,11-undecanediamine, 1,12-dodecanediamine, 1,2-, 1,3- and 1,4-diaminocyclohexane, 1,4-diamino-2,2,6-trimethylcyclohexane (TMCDA), bis (4-aminocyclohexyl ) methane (H12-MDA), bis (4-amino-3-methylcyclohexyl) methane, bis (4-amino-3-ethylcyclohexyl) methane, bis (4-amino-3,5-dimethyl) cyclohexyl) methane, bis (4-amino-3-ethyl-5-methylcyclohexyl) methane (M-MECA), 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane (= isophorone diamine or IPDA), 2- and 4-methyl-1,3-diaminocyclohexane and mixtures thereof, 1,3- and 1,4-bis (aminomethyl) cyclohexane, 2,5 (2,6) -bis (aminomethyl) bicyclo [2.2.1] heptane (NBDA), 3 (4), 8 (9) -bis (aminomethyl) tricycle [5.2.1.02,6] decane, 1,8-menthanediamine, and 1,3- and 1,4-bis (aminomethyl) benzene; primary aliphatic diamines containing an ether group, such as, in particular, bis (2-aminoethyl) ether, 3,6-dioxaoctane-1,8-diamine, 4,7-dioxadecane-1,10-diamine, 4,7-dioxadecane -2,9-diamine, 4,9-dioxadodecane-1,12-diamine, 5,8-dioxadodecane-3,10-diamine, 4,7,10-trioxatridecane-1,13-diamine and higher oligomers of these diamines , 3,9- bis (3-aminopropyl) -2,4,8,10-tetraoxaspiro [5.5] undecane, bis (3-aminopropyl) polytetrahydrofurans and other polytetrahydrofuran diamines, Jeffamine® RFD-270 (from Huntsman), and polyoxyalkylene diamines ("polyether diamines"). The latter are products obtained from the amination of polyoxyalkylene diols and are available, for example, under the name of Jeffamine® (from Huntsman), under the name of Polyetheramine (from BASF) or under the name PC Amine® (from Nitroil) . Particularly suitable polyoxyalkylene diamines are Jeffamine® D-230, Jeffamine® D-400, Polyetheramine D 230, Polyetheramine D 400, PC Amines® DA 250 and PC Amine® DA 400; epolyoxyalkylene triamines ("Polyether triamines"), which are products of the amination of polyoxyalkylene triols and are available, for example, under the trade name Jeffamine® (from Huntsman), under the name Polyetheramine (from BASF) or under the name PC Amine® (from Nitroil), such as, in particular, Jeffamine® T-403, Polyetheramine T403, and PC Amine® TA 403.
    [39] Particularly preferably, polyamine A4 is selected from the group consisting of 1,5-diamino-2-methylpentane, 2,2,4- and 2,4,4-trimethyl hexamethylene diamine, 1,8-octanediamine, 1, 10-decanediamine, 1,12-dodecanediamine, 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane, 2- and 4-methyl-1,3-diaminocyclohexane and mixtures thereof, 1,3-bis (aminomethyl ) cyclohexane, 1,4-bis (aminomethyl) cyclohexane, 2.5 (2.6) - bis (aminomethyl) bicyclo [2,2,1] heptane, 3 (4), 8 (9) -bis (aminomethyl) tricycle [5.2.1.026] decane, bis (2-aminoethyl) ether, 3,6-dioxaoctane-1,8-diamine, 4,7-dioxadecane-1,10-diamine, 4,7-dioxadecane- 2,9- diamine, 4,9-dioxadodecane-1,12-diamine, 5,8-dioxadodecane-3-10-diamine, 1,3-bis (aminomethyl) benzene and 1,4-bis (aminomethyl) benzene.
    [40] These polyamines are particularly easily accessible and, in the reaction with isocyanates, these polyamines lead to urea groups, whose phase separates particularly well. The adhesives produced with this have particularly high resistance, in particular, high modulus of elasticity, and the mechanical properties are not very dependent on temperature.
    [41] Of these, 1,3-bis (aminomethyl) cyclohexane, and 1,3-bis (aminomethyl) benzene are preferred, 1,3-bis (aminomethyl) benzene being the most preferred. These polyamines can be used to produce cured adhesives having particularly high strengths.
    [42] The selection of triol A1, diol A2, aromatic alkoxylated diol A3, and polyamine A4 and the use of them in certain carefully matched reasons provide the adhesive with good processing properties and excellent resistance in the cured state, with regions amorphous and crystalline being present with very good separation, and the mechanical properties are not very dependent on temperature, and the possibility of thermal disconnection of the adhesive bonds in a temperature range of interest being provided.
    [43] In the adhesive, triol A1, diol A2, and alkoxylated aromatic diol A3 are present in a weight ratio of A1 / (A2 + A3) <10.
    [44] Preferably, the A1 / (A2 + A3) weight ratio is in the range of 3 to 10. These adhesives have a particularly advantageous combination of strength and extensibility.
    [45] In the adhesive, diol A2 is present in an amount, such that the A1 / A2 weight ratio between A1 triol and A2 diol <15.
    [46] Preferably, the A1 / A2 weight ratio is 10 or less. This adhesive has high strength and good extensibility.
    [47] Particularly preferably, the A1 / A2 weight ratio is in the range of 5 to 10. This adhesive has a particularly elastic modulus of temperature.
    [48] Preferably, the alkoxylated aromatic diol A3 is present in the adhesive in an amount, such that the A2 / A3 weight ratio is in the range of 0.5 to 7.5, in particular 1.5 to 7.4. These adhesives have high strength and the ability to thermally switch off.
    [49] In one aspect of the invention, the A2 / A3 weight ratio is preferably 3.5 or less, particularly preferably in the range of 0.5 to 3.5, in particular in the range of 0.8 to 3. These adhesives result in adhesive bonds that can be thermally disconnected particularly well.
    [50] In another aspect of the invention, the A2 / A3 weight ratio is preferably 3.5 to 15, particularly preferably in the range 3.5 to 7.5, and in particular, in the range 3.6 to 7.4. These adhesives produce particularly high tensile and shear strengths.
    [51] In another aspect of the invention, the A2 / A3 weight ratio is preferably 3.5 or less, particularly preferably in the range of 0.5 to 3.5, in particular in the range of 0.8 to 2. These adhesives produce particularly high initial resistances, which is particularly advantageous for automated bonding connections since this allows for initial loading of the adhesive bond, which allows for high cycle times. High values for tensile and shear strength during curing are a measure of high initial strength.
    [52] Preferably the polyamine A4 is present in the adhesive in an amount, such that the weight ratio of A1 / (A2 + A4) is in the range of 4.5 to 11. These adhesives exhibit an easy to handle opening time, and good stability during application.
    [53] Particularly preferably, the A1 / (A2 + A4) weight ratio is in the range of 4.5 to 6.5. These adhesives also have high resistance at room temperature and 85 ° C, and a particularly small increase in Young's modulus between room temperature and -35 ° C.
    [54] Particularly suitable as the B1 polyisocyanate are monomeric diisocyanates or triisocyanates, and monomeric diisocyanates or triisocyanate derivatives, polymers and derivatives, and any mixtures thereof.
    [55] Suitable aromatic monomeric diisocyanates or triisocyanates are, in particular, 2,4- and 2,6-tolylene diisocyanate and any mixtures of these isomers (TDI), 4,4'- diisocyanate , 2,4'- and 2,2'-diphenylmethane and any mixtures of these isomers (MDI), 1,3- and 1,4-phenylene diisocyanate, 2,3,5,6-tetramethyl-1,4 -di- isocyanatobenzene, naphthalene-1,5-diisocyanate (NDI), 3,3'-dimethyl-4,4'-diisocyanatodiphenyl (TODI), dianisidine diisocyanate (DADI), 1,3, 5- tris (isocyanatomethyl) benzene, tris (4-isocyanatophenyl) methane, and tris (4-isocyanatophenyl) thiophosphate.
    [56] Suitable aliphatic monomeric diisocyanates or triisocyanates are, in particular, 1,4-tetramethylene diisocyanate, 2-methylpentamethylene-1,5-diisocyanate, 1,6-hexamethylene diisocyanate ( HDI), 2,2,4- and 2,4,4-trimethyl-1,6-hexamethylene diisocyanate (TMDI), 1,10-decamethylene diisocyanate, 1,12-dodecamethylene diisocyanate , lysine diisocyanate and lysine ester, cyclohexane-1,3- and -1,4-diisocyanate, 1-methyl-2,4- and -2,6-diisocyanatocyclohexane and any mixtures of these isomers (HTDI or H6TDI), 1-isocyanate-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (= isophorone diisocyanate or IPDI), perhydro-2,4'- and -4,4'- diisocyanate diphenylmethane (HMDI or H- | 2MDI), 1,4-diisocyanate-2,2,6-trimethylcyclohexane (TMCDI), 1,3-, and 1,4-bis (isocyanatomethyl) cyclohexane, diisocyanate of m - and p-xylylene (m- and p-XDI), m- and p-tetramethyl-1,3- and -1,4-xylylene diisocyanate (m- and p-TMXDI), bis (1-isocyanate -1-methylethyl) naphthalene, d fatty acid isocyanates dimer and trimer, such as 3,6-bis (9-isocyanatononyl) -4,5-di (1-heptenyl) cyclohexene (dimeryl diisocyanate) and tri, isocyanate of a, a, a ', a', a "," -hexamethyl-1,3,5-mesitylene.
    [57] Oligomers, polymers and suitable derivatives of these monomeric diisocyanates and triisocyanates are, in particular, derivatives of MDI, TDI, HDI and IPDI. Of these, particularly suitable are the commercially available types, especially HDI biurets, such as Desmodur® N 100 and N 3200 (from Bayer), Tolonate® HDB and HDB-LV (from Rhodia) and Duranate® 24A-100 (from Asahi Kasei ); HDI isocyanurates, such as Desmodur® N 3300, N 3600 and N 3790 BA (all from Bayer), Tolonate® HDT, HDT-LV and HDT-LV2 (from Rhodia), Duranate® TPA 100 and THA-100 (from Asahi Kasei) and Coronate® HX (from Nippon Polyurethane); HDI uretdiones, such as Desmodur® N 3400 (from Bayer); HDI imino-oxadiazindiones, such as Desmodur® XP 2410 (from Bayer); HDI allophanates, such as Desmodur® VP LS 2102 (from Bayer); IPDI isocyanurates, for example, in solution like Desmodur® Z 4470 (from Bayer) or in solid form like Vestanat® T1890 / 100 (from Degussa); TDI oligomers, such as Desmodur® IL (from Bayer); and mixed isocyanurates based on TDI / HDI, for example, as Desmodur® HL (from Bayer). In addition, particularly suitable are forms of MDI that are liquid at room temperature (so-called "modified MDI"), which are mixtures of MDI with MDI derivatives, in particular carbodiimide MDI or MDI-uretonimines or urethane MDI under commercial names such as Desmodur® CD, Desmodur® PF, Desmodur® PC (all from Bayer) or Isonate® M 143 (from Dow) and mixtures of MDI and MDI counterparts (polymeric MDI or PMDI), available under the trade names such as Desmodur®VL, Desmodur® VL50, Desmodur® VL R10, Desmodur®VL R20, Desmodur®VH 20 N and Desmodur® VKS 20F (all from Bayer), Isonate® M 309, Voranate® M 229 and Voranate ® M 580 (all from Dow) or Lupranat® M 10 R (from BASF). In practice, the oligomeric polyisocyanates mentioned above are generally mixtures of substances with different degrees of oligomerization and / or chemical structures. Preferably, they have an average NCO functionality of 2.1 to 4.0.
    [58] Preferred like polyisocyanate B1 are forms of MDI that are liquid at room temperature. These are, in particular, so-called polymeric MDI and MDI with fractions composed of oligomers or derivatives thereof. The content of MDI (= 4,4'-, 2,4'- and 2,2'-diphenylmethane diisocyanate and any mixtures of these isomers) of these liquid forms of MDI is in particular 50 to 95% by weight 60 to 90% by weight.
    [59] Particularly preferred as the polyisocyanate B1 is the polymeric MDI and, in particular, types of MDI that are liquid at room temperature and contain fractions composed of MDI carbodiimides or adducts thereof.
    [60] Particularly good processing properties and particularly high strengths are achieved with these B1 polyisocyanates.
    [61] Polyurethane polymer B2 preferably has 50 to 95% by weight, in particular 70 to 90% by weight, polyoxyalkylene units, particularly preferably polyoxyethylene and / or polyoxypropylene units, in particular polyoxypropylene units. This polyurethane polymer has low viscosity and allows good extensibility.
    [62] Polyurethane polymer B2 preferably has an average molecular weight of 1,000 to 20,000 g / mol, particularly preferably 2,000 to 10,000 g / mol.
    [63] Polyurethane polymer B2 preferably has an average NCO functionality in the range of 1.7 to 3, in particular 1.8 to 2.5. This polyurethane polymer allows good processing properties and good mechanical properties in the cured state.
    [64] Particularly preferably, polyurethane polymer B2 has an average NCO functionality in the range of 2.05 to 2.5. This polyurethane polymer allows good extensibility at high strength.
    [65] Polyurethane polymer B2 preferably has a free isocyanate group content of 1 to 10% by weight, particularly preferably 1 to 5% by weight.
    [66] The urethane groups and free isocyanate groups of the polyurethane polymer B2 are preferably derived from 4,4'-diphenylmethane diisocyanate. In this sense, particularly good rigid segments are obtained during curing of the adhesive and, thus, particularly high resistances are obtained.
    [67] A suitable polyurethane polymer B2 having isocyanate groups can be obtained by reacting at least one polyisocyanate with at least one polyol. This reaction can occur in such a way that the polyol and the polyisocyanate are made to react using typical processes, for example, at temperatures from 50 ° C to 100 ° C, optionally with the concomitant use of suitable catalysts, where the poly- isocyanate is measured in such a way that the isocyanate groups of the same are present in the stoichiometric excess in relation to the hydroxyl groups of the polyol. Advantageously the polyisocyanate is measured in such a way that an NCO / OH ratio of 1.3 to 5, in particular, of 1.5 to 3, is observed. The "NCO / OH ratio" should be understood as meaning the ratio between the number of isocyanate groups used and the number of hydroxyl groups used.
    [68] Polyols particularly suitable for the preparation of a B2 polyurethane polymer are the following commercially available polyols or mixtures thereof: - Polyoxyalkylene polyols, also referred to as polyether polyols or oligoetherols, which are products of the polymerization of ethylene oxide, oxide 1,2-propylene, 1,2- or 2,3-butylene, oxetane, tetrahydrofuran or mixtures thereof, optionally polymerized using a starting molecule having two or more active hydrogen atoms, such as water, ammonia or compounds having various OH or NH groups, such as 1,2-ethanediol, 1,2- and 1,3-propanediol, neopentyl glycol, diethylene glycol, triethylene glycol, isomeric dipropylene glycols and tripropylene glycols, isomeric butanediols, pentanediols, hexanediols, heptanediols, heptanediols , nonanodiols, decanodiols, undecanodiols, 1,3- and 1,4-cyclohexanedimethanol, bisphenol A, hydrogenated bisphenol A, 1,1,1-trimethylolethane, 1,1,1-trimethylolpropane, glycerol, aniline and mistiline other compounds mentioned above. It is possible to use both polyoxyalkylene polyols with a low degree of unsaturation (measured according to ASTM D-2849-69 and expressed in milliequivalents of unsaturation per gram of polyol (meq / g)), prepared, for example, using so-called double metal cyanide complex catalysts (DMC catalysts), and polyoxyalkylene polyols with a greater degree of unsaturation, prepared, for example, using anionic catalysts, such as NaOH, KOH, CsOH or alkali alkoxides.
    [69] Polyoxyalkylene diols or polyoxyalkylene triols, in particular polyoxyethylene and polyoxypropylene diols and triols, are particularly suitable.
    [70] Polyoxyalkylene diols and triols with a degree of unsaturation of less than 0.02 meq / g and with a molecular weight in the range of 1,000 to 30,000 g / mol, and polyoxypropylene diols and triols with a molecular weight of 400 to 8,000 g / mol are especially suitable.
    [71] So-called ethylene oxide-terminated polyoxypropylene polyols ("EO-coated on the end, ethylene oxide-coated on the end) are particularly suitable. Polyether polyols grafted with styrene-acrylonitrile- or acrylonitrile-methyl methacrylate. Polyester polyols, also referred to as oligoesterols, prepared by methods known, in particular, by the polycondensation of hydrocarboxylic acids or the polycondensation of aliphatic and / or aromatic polycarboxylic acids with di- or polyhydric alcohols.
    [72] Particularly suitable polyester polyols are those which are produced from dihydric to trihydric alcohols, in particular dihydric, such as ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, neopentyl glycol, 1,4-butanediol, 1,5-pentanediol, 3-methyl-1,5-hexanediol, 1,6-hexanediol, 1,8-octanediol, 1,10-decanediol, 1,12-dodecanediol, 1,12-hydroxystearyl alcohol, 1,4-cyclohexanedimethanol, acid diol dimeric fatty (dimerdiol), hydroxypivalic acid neopentyl glycol ester, glycerol, 1,1,1-trimethylolpropane or mixtures of the aforementioned alcohols, and organic dicarboxylic or tricarboxylic acids, in particular, dicarboxylic acids or anhydrides or esters thereof, such as succinic acid, glutaric acid, adipic acid, trimethyladipic acid, submeric acid, azelaic acid, sebacic acid, dodecane dicarboxylic acid, maleic acid, fumaric acid, dimeric fatty acid, phthalic acid, isophthalic acid, terefic acid thallic acid, dimethyl terephthalate, hexahydrophthalic acid, trimellitic acid and trimellitic anhydride, and lactone polyester polyols, such as e-caprolactone and starting compounds, such as the dihydric or trihydric alcohols mentioned above.
    [73] Polyester diols are particularly suitable polyester polyols. Polycarbonate polyols, such as those accessible, for example, by reacting the aforementioned alcohols - used to synthesize polyester polyols - with dialkyl carbonates, diaryl or phosgene carbonates. - Block copolymers carrying at least two hydroxyl groups and including at least two different blocks having a polyether, polyester and / or polycarbonate structure of the type described above, in particular polyester polyether polyols. - Polyacrylate and polymethacrylate polyols - Polyhydroxy-functional fats and oils, for example, natural fats and oils, in particular castor oil; or - so-called oleochemicals - polyols obtained by the chemical modification of natural fats and oils, for example, epoxypolyesters or epoxypolyethers obtained by epoxidation of unsaturated oils and subsequent opening of the ring with carboxylic acids or alcohols, or polyols obtained by the hydroformylation and hydrogenation of unsaturated oils ; or polyols obtained from natural fats and oils by the degradation process, such as alcoholisation or ozonolysis and subsequent chemical bonding, for example, by transesterification or dimerization, of the degradation products or derivatives thereof thereby obtained. Suitable degradation products of natural fats and oils are, in particular, fatty acids and fatty alcohols and fatty acid esters, in particular, methyl esters (FAME), which can be derived, for example, by hydroformylation and hydrogenation to form the hydroxy esters of fatty acids. - Polyhydrocarbon polyols, also referred to as oligohydrocarbons, such as polyhydroxy-functional polyolefins, polyisobutylene, polyisoprene; polyhydroxy-functional diene ethylene-propylene, ethylene-butylene or ethylene-propylene copolymers, for example, those made by Kraton Polymers; polyhydroxy-functional polymers of dienes, in particular, 1,3-butadiene, which can be prepared, in particular, also by anionic polymerization; copolymers of polyhydroxy-functional dienes, such as 1,3-butadiene or mixtures of diene and vinyl monomers, such as styrene, acrylonitrile, vinyl chloride, vinyl acetate, vinyl alcohol, isobutylene and isoprene, for example, acrylonitrile copolymers / polyhydroxy-functional butadiene, such as those that can be produced from epoxides or amino alcohols and acrylonitrile / butadiene copolymers terminated in carboxyl (for example, commercially available under the name Hypro® (formerly Hycar®) CTBN and CTBNX and ETBN from Nanoresins AG, Germany, or Emerald Performance Materials LLC); and polyhydroxy-functional hydrogenated diene polymers or copolymers.
    [74] Preferred polyols for the preparation of a polyurethane polymer B2 are polyoxyalkylene polyols, polyester polyols, polycarbonate polyols and polyacrylate polyols. Polyoxyalkylene polyols, in particular, polyoxypropylene polyols and mixed polyoxyethylene-polyoxypropylene polyols are particularly preferred.
    [75] The polyol for preparing a B2 polyurethane polymer preferably has a molecular weight of 500 to 20,000 g / mol, in particular, 1,000 to 8,000 g / mol.
    [76] The polyol for the preparation of a polyurethane polymer B2 is preferably a diol, a mixture of at least one diol and at least one triol, in particular, a mixture of at least one diol and at least one triol.
    [77] Suitable polyisocyanates for the preparation of a polyurethane polymer B2 are, in particular, the following commercially available polyisocyanates or mixtures thereof: 2,4- and 2,6-tolylene diisocyanate and any mixtures of these isomers (TDI), 4,4'-, 2,4'- and 2,2'-diphenylmethane diisocyanate and any mixtures of these isomers (MDI), 1,3- and 1,4- diisocyanate phenylene, 2,3,5,6-tetramethyl-1,4-diisocyanatobenzene, naphthalene-1,5-diisocyanate (NDI), 3,3'-dimethyl-4,4'-diisocyanatodiphenyl (TODI ), 1,3,5-tris (isocyanatomethyl) benzene, 2-methylpentamethylene-1,5-diisocyanate, 1,6-hexamethylene diisocyanate (HDI), 2,2,4- diisocyanate 2,4,4-trimethyl-1,6-hexamethylene (TMDI), 1,10-decamethylene diisocyanate, 1,12-dodecamethylene diisocyanate, lysine and lysine ester diisocyanate, cyclohexane-1 , 3- and -1,4-diisocyanate, 1-methyl-2,4- and -2,6-diisocyanatocyclohexane, and mixtures of these isomers (HTDI or H6TDI), 1-isocyanate-3,3,5 -trimethyl-5-isocyanatomet yl cyclohexane (= isophorone diisocyanate or IPDI), perhydro-2,4'- and -4,4'-diphenylmethane (HMDI or H12MDI), 1,4-diisocyanate-2,2, 6-trimethylcyclohexane (TMCDI), 1,3- and 1,4-bis (isocyanatomethyl) cyclohexane, m- and p-xylylene diisocyanate (m- and p-XDI) and m- and p- diisocyanate tetramethyl-1,3- and -1,4-xylylene (m- and p-TMXDI). MDI, TDI, IPDI and HDI are preferred. MDI is particularly preferred. 4,4'-diphenylmethane diisocyanate is most preferred. Using this MDI isomer, particularly good rigid segments and, therefore, with particularly high strengths, are obtained during the curing of A2 diols and A4 polyamines.
    [78] Polyisocyanate B1 and polyisocyanate used to prepare polyurethane prepolymer B2 are preferably different types of polyisocyanate.
    [79] Particularly preferably, polyisocyanate B1 is an MDI that is liquid at room temperature, and the polyisocyanate used to prepare polyurethane polymer B2 is 4,4'-diphenylmethane diisocyanate, which is normally solid at room temperature. In this way, the second component is liquid at room temperature, which allows easy processing and allows particularly good mechanical properties. A defined mixture of polyisocyanate B1 and polyurethane polymer B2 can be achieved by first preparing the polyurethane polymer B2 separately before being mixed with polyisocyanate B1.
    [80] Thus, preferably, the preparation of polyurethane polymer B2 does not take place in the presence of polyisocyanate B1.
    [81] The weight ratio between polyisocyanate B1 and polyurethane polymer B2 is preferably 0.25 to 4, preferably 0.25 to 2, particularly preferably 0.3 to 1.5, and in particular , from 0.4 to 1.0. This second component produces adhesives with good processability, high strength and high elongation possible.
    [82] In addition, the polyurethane adhesive may contain other substances that react with the isocyanate groups as part of the first component.
    [83] In particular, the first component can contain at least one polyol and / or at least one low molecular weight dihydric or polyhydric alcohol, which has been mentioned for the preparation of polyurethane polymer B2.
    [84] In addition, the polyurethane adhesive may contain catalysts that accelerate the reaction of hydroxyl groups with isocyanate groups, in particular, organo-tin, organozinc and organobismuth metal catalysts, for example, dibutyltin dilaurate, or tertiary amines, amidines or guanidines , for example, 1,4-diazabicyclo [2.2.2] octane (DABCO) or 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU).
    [85] In addition to those mentioned above, the polyurethane adhesive may contain other constituents that are commonly used in two-component polyurethane compositions, in particular, the following: - plasticizers; - solvents; - inorganic and organic filling materials; - fibers, for example, made of polyethylene; - pigments; - rheology modifiers, in particular, thickeners or thixotropic agents; - drying agents; - adhesive promoters; - stabilizers against oxidation, heat, light and UV radiation; - flame retardant substances; - surfactants, in particular wetting agents, flow control agents, de-aeration agents or defoamers; - biocides, such as algaecides, fungicides or fungal growth inhibitors.
    [86] When using other constituents of the polyurethane adhesive, it is advantageous to ensure that they do not significantly impair the storage stability of the specific component. If these substances should be stored together with isocyanates, this means, in particular, that they should not contain any, or at most, traces of water. It may be useful to dry certain constituents chemically or physically before mixing them.
    [87] The components of the polyurethane adhesive are advantageously formulated, such that the volume mixing ratio of the first and second components is in the range of 1: 3 to 3: 1, in particular, 1: 2 to 2: 1. Preferably, this ratio is approximately 1: 1.
    [88] The mixing ratio is preferably defined, such that in the mixed polyurethane adhesive, the ratio between the number of isocyanate groups and the number of reactive isocyanate groups, in particular, the sum of OH and NH2 groups, before curing is approximately in the range of 1.2 to 1, preferably from 1.1 to 1.
    [89] The two components are prepared separately from each other and at least for the second component, usually in the absence of moisture. Typically, the components are stored in each case in a separate container. The other constituents of the polyurethane adhesive may be present as part of the first or second component, wherein the other isocyanate-reactive constituents are preferably part of the first component. A suitable container for storing each component is in particular a drum, barrel, bag, bucket, can, cartridge or tube.
    [90] Before application, the two components are stored separately from each other and are mixed with each other only during or just before application. The components are advantageously present in a package made up of two separate chambers.
    [91] In another aspect, the invention comprises a package consisting of a package having two separate chambers, which each contain one of the two components of the polyurethane adhesive.
    [92] Preferred packages of this type are, on the one hand, adjacent double cartridges or coaxial cartridges, in which two tubular chambers are arranged close to or within each other and are hermetically sealed and moisture-proof by a piston. When advancing these pistons, the components can be pressed out of the cartridge. The sides of the tubes opposite the piston, if appropriate, are modified by means of an adapter, so that the chamber openings are connected directly to each other in the opening area by a dividing wall. Advantageously, a thread is provided in the area of the chamber outlet opening, so that a static mixer or dynamic mixer can be mounted securely. These packages are particularly preferred for small applications, in particular, for loads up to 1 liter.
    [93] For applications in large quantities, especially for applications in industrial production, advantageously, the two components are filled and stored in drums or vats. During application, the components are pressed out by means of feed pumps and the measurement takes place through lines of a mixing device, such as those commonly used for two-component adhesives in industrial production.
    [94] Mixing is usually done using static mixers or dynamic mixers. When mixing, care must be taken to ensure that the two components are mixed homogeneously as far as possible. If the two components are poorly mixed, local variations of the advantageous mixing ratio will occur, which can cause a deterioration of the mechanical properties. In order to visually control the mixing quality, it can be advantageous if the two components have two different colors. A good mix is considered to exist when the mixed adhesive has a homogeneously mixed color, with no visible scratches or stains.
    [95] After contact of the first component with the isocyanate groups of the second component, curing begins by chemical reaction. Here, the amino groups of polyamine A4 and the hydroxyl groups of triol A1, diol A2, and diol A3 and substances reactive to other isocyanate groups, optionally present, react with the isocyanate groups that are present. Excess isocyanate groups react with the moisture that is present. As a result of these reactions, the polyurethane adhesive cures to form a solid material. This process is also referred to as crosslinking.
    [96] Another aspect of the present invention relates to a method for bonding a first substrate to a second substrate, comprising the following steps: - mixing the two components described above, - applying the polyurethane adhesive mixed with at least one of the surfaces of the substrate to be bonded, - joining the substrates to be bonded within the opening time, - curing the polyurethane adhesive.
    [97] The two substrates can be made of the same or different materials. This method results in an adhesive bond.
    [98] In this bonding method, suitable substrates are, in particular glass, glass ceramics; metals and alloys, such as aluminum, iron and non-ferrous metals, as well as finished surface metals and alloys, such as galvanized or chrome-plated metals; coated and painted substrates, such as powder-coated metals or alloys and painted metal sheets; plastic materials such as polyvinyl chloride (hard and soft PVC), acrylonitrile-butadiene-styrene copolymers (ABS), polycarbonate (PC), polyamide (PA), polyesters, poly (methylmethacrylate) (PMMA), polyester, epoxy resins , polyurethanes (PUR), polyoxymethylene (POM), polyolefins (PO), polyethylene (PE) or polypropylene (PP), ethylene / propylene copolymers (EPM) and ethylene / propylene / diene (EPDM) terpolymers, in which the materials plastics can be surface treated, preferably by means of plasma, corona or flames; fiber-reinforced plastic materials, such as carbon fiber-reinforced plastic materials (CFRP), glass fiber-reinforced plastic materials (GRP) and sheet-forming compounds (SMC); wood, resin-bound wood products, such as phenolic resins, melamine or epoxy, textile resin composites and other so-called polymer composites; and concrete, mortar, brick, tile, plaster and natural stones, such as granite or marble.
    [99] In this method, a substrate is, or both substrates, preferably a metal or ceramic or glass fiber reinforced plastic material or carbon fiber reinforced plastic material.
    [100] If necessary, substrates can be pre-treated before applying the adhesive. Such pretreatments include, in particular, chemical cleaning and / or physical appearance methods, and application of an adhesive promoter, a promoter solution or an adhesive primer.
    [101] This method described for bonding results in an article, in which the adhesive connects to two substrates with each other in a form of adjustment by force. This article is, in particular, a structure, such as a bridge, an industrial item or a consumer item, in particular, a window, a rotor blade of a wind turbine or a means of transport, in particular, a vehicle , preferably an automobile, a bus, a truck, a train or a boat, as well as an airplane or a helicopter; or fixing such an article.
    [102] The invention also relates to an article obtained from the method for bonding described above.
    [103] It may be advantageous if the method of bonding, after the curing step of the polyurethane adhesive includes another step of - heating the adhesive bond containing the cured polyurethane adhesive to separate or disconnect the adhesive bond.
    [104] Heating is preferably carried out here at a temperature of at least 120 ° C, preferably in the range of 140 ° C to 200 ° C, particularly preferably in the range of 150 to 160 ° C, for a period of at least 10 minutes, preferably particularly 20 minutes, particularly preferably for 20 to 180 minutes, more preferably for 25 to 45 minutes.
    [105] Heating is done, in particular, by means of an infrared radiator, hot air dryer, induction heater or in an oven.
    [106] Heating leads to a weakening of the cured adhesive in terms of its strength. Thus, the substrates can be separated mechanically separated from the adhesive using a relatively small expenditure of force, i.e., the adhesive bond is easily separable. The small amount of force used here refers to less than 2 MPa, in particular, a force in the range of 1.5 to 0.2 MPa.
    [107] Particularly good properties for separation are shown by adhesives containing a certain amount of alkoxylated aromatic diol A3, in particular those adhesives in which the A2 / A3 weight ratio is 3.5 or less.
    [108] The possibility of thermally separating the adhesive connections is very advantageous, particularly when repairing a connected workpiece, since substrates with a damaged or defective connection can be easily replaced by heating the adhesive connection. For example, in a vehicle, the parts of which are connected by an adhesive according to the invention, a single adhesive bond can be selectively heated and thus separated, without harming the rest of the vehicle.
    [109] The described polyurethane adhesive has very good properties as a structural adhesive.
    [110] In this case, a structural adhesive refers to an adhesive that forms part of the supporting structure of the connected components in the cured state. Thus, the structural adhesive is an important link in the construction within which it connects two components or substrates. In this sense, high demands are placed on its mechanical properties.
    [111] Another important property of a structural adhesive is its good processability. Here, the two components, individually and during mixing, must have a low viscosity so that they are easily handled and mixed, but then they develop that viscosity very quickly such that a stable pseudoplastic material is immediately obtained, so that layer thicknesses up to 10 mm and more can be applied.
    [112] Using the polyurethane adhesive described, these requirements can be particularly well met. Examples
    [113] Exemplary embodiments are shown below, intended to illustrate the invention described in more detail. Certainly, the invention is not limited to the exemplary embodiments described. 1. Substances used:

    [114] Polymer 1 was prepared by reacting 1300 g of polyoxypropylene diol (Acclaim® 4200 N from Bayer; OH number 28.5 mg KOH / g), 2600 g of polyoxypropylene polyoxyethylene triol (Caradol® MD34- 02 from Shell; OH number of 35.0 mg KOH / g), 600 g of 4,4'-methylenediphenyl diisocyanate (Desmodur® 44 MC L, from Bayer) and 500 g of diisodecyl phthalate, from according to the known method at 80 ° C to generate an NCO-terminated polyurethane polymer having a content of free isocyanate groups of 2.1% by weight. [2] Preparation of polyurethane adhesives
    [115] For each adhesive, the ingredients specified in Tables 1 and 2 were processed in the amounts indicated (in parts by weight) for the first component ("component 1") using a vacuum solvent in the absence of moisture to form a homogeneous and stored paste. Likewise, the ingredients of the second component ("component 2") specified in Tables 1 and 2 have been processed and stored. Then, the two components were processed for 30 seconds to form a homogeneous paste using a SpeedMixer® (DAC 150 FV, Hauschild), and the paste was tested immediately as follows:
    [116] To determine the mechanical properties, the adhesive was shaped like a dumbbell, according to ISO 527, part 2, 1B and was stored or cured for 24 h at 25 ° C and then for 3 h at 80 ° C.
    [117] After a conditioning time of 24 hours at the temperature (-35 ° C or 23 ° C or 85 ° C) specified in Tables 1 and 2, the modulus of elasticity in the range of 0.05 to 0.25% of elongation ("Young's modulus"), tensile strength and elongation at break of the specimens so prepared were measured in each case, according to ISO 527 on a Z020 Zwick testing machine at the temperature specified in the table and a test speed 50 mm / min.
    [118] To measure the tensile and shear strength, several test specimens were prepared, in which 1 minute after the completion of the mixing time. The adhesive was applied between two steel sheets painted cataphorically which were degreased with isopropanol, in a layer thickness of 2.0 mm, and to an overlapping adhesive surface of 15 x 45 mm. The tensile and shear strength of these test specimens was determined according to DIN EN 1465, in which the test specimens were stored under different conditions before measurement: both for 1 h at 23 ° C; as for 3 h at 23 ° C, or for 12 h at 23 ° C, then for 3 hours at 80 ° C, and then conditioned for 24 h at 23 ° C.
    [119] The results are shown in Tables 1 and 2.
    [120] The information A1 / (A2 + A3), A1 / A2, A2 / A3 and A1 / (A2 + A4) in Tables 1 and 2 refer to the weight ratios of the A1 triols, A2 diols, alkoxylated aromatic diols A3 and A4 polyamines that are present in the respective adhesive.
    [121] Table 3 shows separation tests. For this, adhesives EZ 1 to EZ 3, Ref. 1 and Ref. 3 were used to prepare adhesive bonds in the form of test specimens to determine the tensile and shear strength, as previously described. All test specimens were stored for 12 h at 23 ° C, then for 3 h at 80 ° C, and then conditioned for 24 hours at 23 ° C before each being heated differently in an oven, as indicated in Table 3. After heat treatment, the test specimens were conditioned for 24 hours at 23 ° C, and then, the tensile and shear strength was determined.
    [122] Figure 1 shows the DMTA measurements of films cured for 7 days under standard conditions (23 ° C, 50% relative humidity), performed using a Mettler DMA / SDTA 861 e. The measurement conditions were: Shear measurement, 10 Hz excitation frequency and heating rate of 5 K / min. The test specimens were samples molded on disc (thickness 2-3 mm, diameter 10 mm). These were cooled to -60 ° C and then heated to 200 ° C, while the complex shear modulus G * [MPa] was determined.
    [123] Adhesives EZ-1 to EZ-6 are examples according to the invention, adhesives Ref. 1 to Ref. 5 are comparative examples.
    [124] Immediately after mixing the two components, all prepared adhesives showed a stable consistency.
    [125] One minute after the completion of the mixing time of the two components, the EZ-3 adhesive was applied to a glass fiber-reinforced plastic plate that was previously degreased with isopropanol and covered with a second identical plate, forming an area superimposed adhesive of 15 x 45 mm in a layer thickness of 2 mm, cured for 24 h at 23 ° C and then for 3 hours at 80 ° C, and after a conditioning time of 24 h at 23 ° C, the resistance to tensile and shear was determined as previously described, resulting in a cohesive fracture pattern.
    [126] Likewise, two carbon fiber-reinforced plastic plates were bonded with the EZ-3 adhesive and the tensile and shear strength was determined at 23 ° C, resulting in a fractured pattern.
    Table 1: Composition of properties from EZ 1 to EZ 6 (quantities in parts by weight) "nd" means "not determined"

    Table 2: Composition and properties of Ref. 1 to Ref. 5 (quantities in parts by weight) "na" means "not determined"
    Table 3:
    [127] From Table 3 and Figure 1, it can be seen that thermal destabilization occurs with adhesives according to the invention at temperatures above 140qC, which cannot be detected to the same degree in adhesives Ref.1 and Ref. 3.
    权利要求:
    Claims (15)
    [0001]
    1. Polyurethane adhesive composed of a first and a second component, characterized by the fact that - the first component contains a) at least one triol A1 having a molecular weight in the range of 1,000 to 10,000 g / mol, b) at least one diol A2 having two primary hydroxyl groups and a molecular weight in the range 60 to 150 g / mol, and c) at least one alkoxylated aromatic diol A3 having a molecular weight in the range 300 to 1,000 g / mol, and d) at least one polyamine aliphatic A4 having a molecular weight in the range of 60 to 500 g / mol, where the aliphatic polyamine A4 is an amine with two or three aliphatic amino groups, selected from: - primary aliphatic, cycloaliphatic, or arylaliphatic diamines, - primary aliphatic diamines containing ether groups, and - polyoxyalkylenetriamines which are products of the amination of polyoxyalkylenotriols; and - the second component contains e) at least one polyisocyanate B1 and f) at least one polyurethane polymer B2 having isocyanate groups; - in which triol A1, diol A2 and alkoxylated aromatic diol A3 are present in an amount such that g) the weight ratio A1 / (A2 + A3) <10, and h) the weight ratio A1 / A2 <15.
    [0002]
    2. Polyurethane adhesive according to claim 1, characterized in that the A1 triol is a polyether triol.
    [0003]
    3. Polyurethane adhesive according to claim 1 or 2, characterized in that the triol A1 has primary hydroxyl groups.
    [0004]
    Polyurethane adhesive according to any one of claims 1 to 3, characterized in that the diol A2 is selected from the group consisting of 1,3-propanediol, 1,4-butanediol and 1,5-pentanediol.
    [0005]
    Polyurethane adhesive according to any one of claims 1 to 4, characterized in that the alkoxylated aromatic diol A3 is an ethoxylated and / or propoxylated and / or butoxylated aromatic diol.
    [0006]
    6. Polyurethane adhesive according to claim 5, characterized in that the alkoxylated aromatic diol A3 is a propoxylated bisphenol A or a propoxylated bisphenol A.
    [0007]
    7. Polyurethane adhesive according to any one of claims 1 to 6, characterized in that the polyamine A4 is selected from the group consisting of 1,5-diamino-2-methylpentane, 2,2,4- and 2, 4,4-trimethylhexamethylene diamine, 1,8-octanediamine, 1,10-decanediamine, 1,12-dodecanediamine, 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane, 2- and 4-methyl-1, 3-diaminocyclohexane and mixtures thereof, 1,3-bis (aminomethyl) cyclohexane, 1,4-bis (aminomethyl) cyclohexane, 2,5 (2,6) -bis (aminomethyl) bicycle [2.2.1] heptane, 3 (4), 8 (9) -bis (aminomethyl) tricycle [5.2.1.02,6] decane, bis (2-aminoethyl) ether, 3,6-dioxaoctane-1,8-diamine, 4,7-dioxadecane-1 , 10-diamine, 4,7-dioxadecane-2,9-diamine, 4,9-dioxadodecane-1,12-diamine, 5,8-dioxadodecane-3,10-diamine, 1,3-bis (aminomethyl) benzene and 1,4-bis (aminomethyl) benzene.
    [0008]
    Polyurethane adhesive according to any one of claims 1 to 7, characterized in that the weight ratio A1 / (A2 + A3) is in the range 3 to 10.
    [0009]
    Polyurethane adhesive according to any one of claims 1 to 8, characterized in that the A1 / A2 weight ratio is in the range of 5 to 10.
    [0010]
    Polyurethane adhesive according to any one of claims 1 to 8, characterized in that the A2 / A3 weight ratio is in the range of 0.5 to 7.5.
    [0011]
    11. Polyurethane adhesive according to any one of claims 1 to 10, characterized in that the polyisocyanate B1 is a form of diisocyanate of 4,4'-, 2,4'- and 2,2 '-diphenylmethane which is liquid at room temperature and arbitrary mixtures of these isomers (MDI) in the form of polymeric MDI or MDI with fractions of oligomers or derivatives.
    [0012]
    Polyurethane adhesive according to any one of claims 1 to 11, characterized in that the urethane groups and the free isocyanate groups of the polyurethane polymer B2 are derived from the 4,4'-diphenylmethane diisocyanate.
    [0013]
    13. Method for bonding a first substrate to a second substrate, characterized in that it comprises the following steps: - mixing the two components of a polyurethane adhesive, as defined in any one of claims 1 to 12, - application of polyurethane adhesive mixed with at least one of the substrate surfaces to be bonded, - joining the substrates to be bonded within the opening time, and - curing the polyurethane adhesive.
    [0014]
    Method according to claim 13, characterized in that a substrate is, or both substrates are, a metal or a ceramic or a glass fiber reinforced plastic material or a carbon fiber reinforced plastic material.
    [0015]
    15. Article characterized by the fact that it is obtained from a connection method, as defined in any of claims 13 or 14.
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    JP2015529259A|2015-10-05|
    引用文献:
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    法律状态:
    2018-03-06| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2018-03-13| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2018-03-20| B06I| Publication of requirement cancelled [chapter 6.9 patent gazette]|Free format text: ANULADA A PUBLICACAO CODIGO 6.6.1 NA RPI NO 2462 DE 13/03/2018 POR TER SIDO INDEVIDA. |
    2019-12-03| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2020-05-05| B06A| Notification to applicant to reply to the report for non-patentability or inadequacy of the application [chapter 6.1 patent gazette]|
    2020-08-18| B09A| Decision: intention to grant|
    2020-12-08| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 20/08/2013, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    EP12181776.1|2012-08-24|
    EP12181776.1A|EP2700666A1|2012-08-24|2012-08-24|Structural polyurethane adhesive|
    PCT/EP2013/067345|WO2014029787A1|2012-08-24|2013-08-20|Structural polyurethane adhesive|
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