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    • 专利摘要:
    The present invention relates to an acrylated and / or methacrylated urethane oligomer obtained by reacting a specific polyamine a) with a cyclic carbonate compound b) bearing cyclic carbonaceous groups, giving an intermediate product c) bearing u-shaped urethane groups containing residual amine -NH- reactive groups and then adding reaction of each of said amine reactive residual groups of said product c) to an acrylate group of a compound d) bearing in addition to said acrylate group of additional acrylate and / or methacrylate groups, with each amine -NH- reactive residue group of said product c) thus being converted into a carbon-nitrogen bond bearing said acrylate and / or methacrylate groups and thus obtaining said urethane oligomer, with each carbon-nitrogen bond formed bearing acrylate groups and and / or methacrylates and said urethane oligomer carrying mg urethane and alpha or beta hydroxyl group moieties of said urethane and having acrylate and / or methacrylate functionality ranging from m * p (n-1) to m * p (2n-2). The invention also relates to a process for preparing said oligomer in two stages, the intermediate product c) and the use of said urethane oligomer in crosslinkable compositions, in particular in coating compositions, adhesives, 3D objects obtained layer-by-layer, 3D printing, molding, sealant, chemical sealant, concrete or composite.
    公开号:FR3027306A1
    申请号:FR1459890
    申请日:2014-10-15
    公开日:2016-04-22
    发明作者:Guillaume Monnier；Catherine Leroy
    申请人:Arkema France SA；
    IPC主号:
    专利说明:

    [0001] The invention relates to novel monofunctional urethane oligomers methacrylate or multifunctional acrylates in acrylate and / or methacrylate groups, with the urethane group being obtained without any use of isocyanate, by carbonate-amine reaction which is favorable to the environment and the environment. health.
    [0002] The invention uses a NIPU route which corresponds to "Non-Isocyanate Polyurethane", ie "polyurethane without isocyanate". It allows the selective production of acrylate groups and / or methacrylates with a minimum functionality of 1, but which can be high and in addition to this functionality, a hydroxyl function urethane bond created. These oligomers can be used as crosslinkable binders for coating, adhesive, molding or sealant compositions, concrete, chemical sealing, layer-by-layer 3D object manufacturing systems, coating systems, and the like. 3D printing or concrete or composite. Current synthesis of urethane (meth) acrylate oligomers involves the use of isocyanate or polyisocyanate compounds for multifunctional oligomers. These compounds are toxic and their handling and use require special and strict precautions to preserve human health and the environment in general. In addition, the urethanization reaction (urethane linkage formation by reaction of alcohol with isocyanate) commonly uses tin catalysts, which are also toxic and environmentally harmful compounds.
    [0003] In recent years, there has been a significant development of the carbonate-amine reaction as an alternative route for the formation of a urethane linkage without the use of isocyanates. This reaction makes it possible to access hydroxyl urethane compounds without release of secondary compounds when it involves a cyclic carbonate, that is to say a carbonate ring with 5 or 6 atoms with hydroxyls in respective positions in beta and in gamma of the urethane group. The so-called "Non-Isocyanate Polyurethanes" or "NIPU" abbreviated compounds are then obtained. Carbonates are considered to be harmless or dangerous in general. On the other hand, it is possible to prepare these carbonates by adding CO 2 to an epoxy function of an epoxidized compound. The preparation of said carbonates by such a route therefore consumes CO2, which is a greenhouse gas. Thus, subject to adopting this method of preparation, substitution of the alcohol-isocyanate reaction by the carbonate-amine reaction is beneficial both in terms of safety and the environment in general. The object of the present invention relates to novel urethane acrylate or methacrylate oligomers of well controlled and reproducible structure in terms of chain length and functionality, in particular without a crosslinked structure when reacting a polyamine carrying 2 to 5 primary amine groups. and / or - 2 - secondary on a carbonate compound that can carry up to two cyclic carbonate functions. These oligomers can be monofunctional, both in acrylates and in methacrylates, and / or especially multifunctional oligomers in acrylates and / or methacrylates and more particularly in functionality of at least 3, which are suitable for crosslinking by UV radical or peroxide or dually, the dual route being a mixed route using a peroxide thermally and a photoinitiator UV. The present invention makes it possible in particular to access such oligomers urethanes acrylates or methacrylates, without particular restriction in the handling or storage of raw materials used, non-toxic and friendly to human health and the environment in general and commercially available. The present invention relates more particularly to oligomers bearing urethane aminoacrylate groups and as final reactive groups of the acrylates and / or methacrylates and hydroxyls in the beta or gamma position of said urethane link depending on the number of carbon ring atoms in each case. 6 atoms. The urethane and hydroxyl groups generated are different in number (lower) and in positioning of the urethane linkage independent of the acrylate or methacrylate groups without a direct urethane-acrylate ester or methacrylate ester linkage. There is thus a multiplier effect on the final functionality of the oligomer of the invention in acrylate and / or methacrylate groups, with a control of the structure and the functionality of said oligomers and without the risk of formation of gels during their preparation. especially when multifunctional oligomers of acrylates and / or methacrylates are targeted. In particular, these oligomers have a very satisfactory crosslinking rate under UV and they make it possible to obtain crosslinked finished application products, in particular coatings, having a good flexibility and a hardness that can be adjusted according to the choice of reactants. Thus, the coatings obtained have in particular a good compromise of performance between hardness and flexibility while having the advantages of the presence of urethane and aminoacrylate groups in addition. These advantages are in particular: chemical resistance, solvent resistance, abrasion and wear resistance and synergistic activator effect of aminoacrylate bonds during photocrosslinking. The other particular advantage of the invention is that it makes it possible to obtain polyurethane multiacrylate and / or multimethacrylate oligomers by a simpler method and in only two steps compared with the multiple steps often necessary in the usual processes for obtaining oligomers. acrylated and / or methacrylated urethanes. The first subject of the invention relates to a monofunctional or multifunctional urethane oligomer made of acrylates and / or methacrylates, obtained from the reaction of a specific polyamine a) with a cyclic carbonate compound b), said polyamine being in excess stoichiometric and giving an intermediate product c) carrying amine reactive residual groups and in a second step, adding each of said amine -NH- reactive residual groups to an acrylate group of a compound d) bearing in addition to said acrylate group, groups additional acrylates or methacrylates, with obtaining said urethane oligomer according to the invention. The present invention also relates to a process for the preparation of said oligomer comprising two steps: i) reaction of said polyamine a) on said carbonate b) giving said intermediate product c) and ii) modification reaction of said product c) by Michael addition reaction each of said amine -NH- reactive residual groups on an acrylate group of said compound d). Another subject of the invention relates to a crosslinkable composition comprising at least one oligomer as defined according to the present invention. The present invention also covers the use of said oligomer as a reactive binder in coating compositions including paints, varnishes, inks, adhesive compositions, molding compositions, sealant compositions, chemical sealant compositions, system compositions, and the like. manufacturing objects in 3D layer by layer, compositions of 3D printing systems, concrete compositions or composite compositions. Finally, the present invention covers the finished product which results from the use of at least one oligomer as defined according to the invention or an oligomer as obtained by the process of the invention, this finished product being preferably chosen among: coatings including paints, varnishes and inks, adhesives, molded parts, 3D objects obtained layer by layer, 3D printing objects, gaskets, chemical sealing, concrete finished or composite articles. The first subject of the invention therefore relates to a monofunctional or multifunctional urethane oligomer in acrylates and / or methacrylates, preferably acrylates, which can be obtained from the reaction of a specific polyamine a) with a cyclic carbonate compound b) carrying cyclic carbonyl groups, said polyamine being in stoichiometric excess with respect to b) and said reaction giving an intermediate product c) bearing urethane groups formed, carrying amine -NH- reactive residual groups and then by a reaction addition of each of said amine reactive residual groups of said product c) to an acrylate group of a compound d) bearing, in addition to said acrylate group, additional acrylate and / or methacrylate groups, with each residual amine reactive group; -NH- of said product c) thus being converted into a carbon-nitrogen bond bearing said groups a thereby obtaining said urethane oligomer, with said polyamine a) bearing n primary and / or preferably from 2 to 4 and more preferably from 2 to 3, even more preferably from 2, - said carbonate b) carrying cyclic carbonic groups with m ranging from 1 to 2, preferably the cycle of said cyclic carbonate groups being a ring. at 5 or 6 atoms, - said intermediate product c) carrying u urethane groups and m OH groups alpha or beta of said urethane group and c) carrying m * (n-1) to m * (2n- 2) amine -NH- reactive residual groups, - said compound d) bearing acrylate and / or methacrylate groups in addition to said acrylate group which reacts with one of said amine -NH- reactive residual groups with p being at least equal to 1 and preferably at least 2 and the number of said amine -NH- reactive residual groups of said product c) being less than or equal to the number of moles of said compound d) - each carbon-nitrogen bond formed being carrier of acrylate and / or methacrylate groups and said urethane oligomer carrying u urethane groups and alpha or beta hydroxyl groups of said urethane and having a functionality of acrylates and / or methacrylates ranging from m * p (n-1) to m * p (2n-2). Said n primary and / or secondary amine groups of said polyamine a) may be borne by an A radical of valence n, which radical A may be or comprise an aliphatic, cycloaliphatic or aromatic structure with in the latter case said n amine groups being carried by at least one alkylene group attached to the aromatic ring and the rings of said m cyclic carbonate groups of said carbonate b) are 5 or 6 atoms and borne by a radical R 3 of valence m, with R 3 being a hydrocarbon radical of aliphatic, cycloaliphatic or aromatic and optional hydroxyl or R3 may be a simple hydrogen for m = 1, optionally the carbonate ring may be substituted with a substituent R4 hydrocarbon optionally hydroxyl, R4 may be of aliphatic structure, cycloaliphatic or aromatic identical or different from that of R3 and possibly able to form a ring attached to the carbonate ring by two atoms of common carbon. The term "reagent" relating to said amine -NH- reactive residual groups means according to the present invention "capable of reacting by Michael addition to an acrylate function with formation of an aminoacrylate -N-CH2-CH2-OO2-" group. On the basis of said radical A, said polyamine a) may be broadly represented by: (R'1-NH-) A (-NH2) y, with R'1 being alkyl or cycloalkyl or aralkyl and with x + y = n . The cycloaliphatic structure as mentioned above includes polycyclic structures such as aliphatic bicycles or tricycles. More particularly, said polyamine a) may have an aliphatic structure of from 02 to 054 or a cycloaliphatic structure including a polycyclic one as a bicycle or tricycle, or it may comprise an aromatic structure with the amine functional groups carried by alkylenes attached to the aromatic ring.
    [0004] Said polyamine a) may have a monomeric structure and therefore no repeating or oligomeric unit with at least two repeating monomeric units linked to an amine group, for example alkylene imine as a repeating unit, in particular ethylene imine or to another group such as an ether, ester or amide. According to a particular option related to the structure of the radical A of said polyamine a) carrying said n primary and / or secondary amine groups, said polyamine a) is chosen from: an alkylene polyamine O 2 to O 5, said alkylene being O 2 to 054 linear or branched and bearing said n primary and / or secondary amine groups, - a polyamine comprising at least two repeating units among: alkylene imine in 02 to 04, in particular ethylene imine or propylene imine, preferably ethylene imine, said polyamine has ) being in this case an oligoalkylene imine polyamine, in particular a polyethylene imine polyamine including a dendritic structure, - a polyamine comprising one or more units among: ether, ester-amide, amide, with in the case of the presence of several units, said polyamine a) being chosen from: oligoether polyamines, oligoester amide-polyamines or multiester amide-polyamines. Among the polyamines a) at 02 to 054, mention may be made of linear aliphatic chain diamines or triamines among the alkylenes diamines or alkylenes triamines, including the fatty diamines in 036 OR or fatty triamines in 054, with said alkylenes being able to be alkoxylated or non-alkoxylated. Among the polyamines, one or more units among: ether, ester-amide, amide, mention may be made in the case of several units, the polyethylenes imines polyamines, preferably oligoethylene imine polyamines, the oligoether polyamines such as Jeffamines R, the oligoester-amide polyamines or the multi (ester-amide amines) which are completed multifunctional esters (each ester) with an amide-amine group. As regards said overall functionality of said urethane oligomer according to the invention, it may have the minimum value when all the amine groups of the polyamine a) are all secondary and the maximum value when all the amine groups of the polyamine a) are primary. Therefore, this functionality can only vary between the two limits as defined. According to one particular variant, said polyamine a) is chosen from the polyamines of the following formulas a1) or a2): a1) R1-NH-R2- (NH-R) (NH-R11 with n1 being equal to 3, 2, 1 or 0 and preferably n1 being 2, 1 or 0 a2) R1-NH- (R'2NH), 2-R "2-NH-R 'with n2 being equal to 3, 2 or 1 with R1 and R1; and R 'being independently selected from: H, alkyl, preferably C1-C3, optionally said alkyl being alkoxylated or a cyclolalkyl, with R1 being the same or different from R and R' and with R and R 'being the same or different and in particular with R and / or R 'being different from H, R2 being alkylene or cycloalkylene (comprising a C6 aliphatic ring) or aralkylene of valence n ranging from 2 to 5, with R2 being able to carry or comprise at least one group tertiary amine and R'2 and R "2 may be identical or different and selected from alkylene, preferably C2 to Cg, more preferably C2 to C6 and if R" 2 is different from R'2 in this case R "2 may carry or include at least one tertiary amine group. According to a particular embodiment of said oligomer according to the invention, said polyamine a) is an amine according to formula a2) defined above, with n2 = 1 and R1 and R 'being H and R'2 and R "2 being identical alkylenes. or different and from C2 to C6, in particular C2 to C4, more particularly said amine a2) being selected from 3 (2-aminoethyl) aminopropylamine or bis (3-aminopropyl) amine According to a particular choice, said polyamine a) is an amine defined according to formula a2), as described above with n2 = 2 or 3 and R1 and R 'being H and R'2 and R "2 being identical C2-C4, in particular C2-C3, alkylenes, more particularly said amine a2) being selected from triethylenetetramine or tetraethylenepentamine. More particularly, said polyamine is a diamine (n = 2) and preferably selected from secondary-primary diamines, more preferentially from: N-methyl-1,3-propane diamine, N-methylethane diamine, N-methyl-1, 4- butane diamine, N-methyl 1,5-pentanediamine.
    [0005] According to a second particularly preferred option, said polyamine a) is a diamine (n = 2) and is secondary-secondary, more preferably: N-methyl, N'-methyl-1,3-propane diamine, N-methyl, N'-methyl-ethane diamine, N-methyl, N'-methyl 1,4-butane diamine, N-methyl, N'-methyl 1,5-pentanediamine. The carbonate compound b) according to the invention can be represented overall by the global formula Ra (-cyclecarbo), with m ranging from 1 to 2 and "cyclecarbo" being said cyclic carbonate group. Said compound b) may be a mixture of carbonate compounds bearing m = 1 and / or m = 2 cyclic carbonates. When m is between 1 and 2, it is a mixture of at least one monocarbonate b) with m = 1 and at least one dicarbonate b) with m = 2.
    [0006] The polyamine a) may also be a mixture of different polyamines a) of different nature and / or with n different or identical. The compounds d) may also be a mixture of at least two compounds d) according to the invention of different nature with a different or identical functionality. The definition of said hydrocarbon radical R 3 bearing cyclic carbonate moieties in said cyclic carbonate compound b) depends on the structure of said carbonate b). In particular, said carbonate b) is a complete or partial ester of a polyacid, monomeric or oligomeric such as a polycarbonate oligoester, with a hydroxylated carbonate, preferably glycerol carbonate or b) is a complete or partial ether of a monomeric or oligomeric polyol such as oligoester or oligoether polyol with a hydroxyl carbonate, preferably gycerol carbonate or b) is a complete or partial ether of a phenolic derivative, including bisphenol A or dihydroxy-phenylene with a hydroxylated carbonate, preferably the glycerol carbonate or b) is an allylic or vinyl alcohol ether with a hydroxylated carbonate, preferably glycerol carbonate or a methacrylate of a hydroxyl carbonate, preferably glycerol carbonate or b) is a carbonate obtained by addition of CO2 to an epoxidized monomeric or oligomeric precursor compound or b) is the product of the reaction of dimethylcarbonate with an alipol at least 2, preferably from 2 to 6. More particularly, said epoxidized precursor may be an epoxidized oligodiene, a methyl or ethyl ester of an epoxidized unsaturated fatty acid or an epoxidized derivative of an epoxide. unsaturated fatty alcohol (monounsaturated or diunsaturated fatty chain) or an epoxidized prepolymer obtained by amine-epoxide reaction, epoxidized polyester epoxy prepolymer by anhydride-epoxy reaction, epoxidized acrylic oligomer and / or epoxidized styrenic oligomer or a glycidyl ether alcohol with a polyol or a glycidyl ester alcohol with a polyacid, with said polyol or polyacid which can be monomeric or oligomeric or an epoxidized olefin (for m = 1) or an epoxidized diolefin. Thus, when said epoxidized precursor is an epoxidized oligodiene or an epoxidized unsaturated fatty acid ester or an epoxidized unsaturated fatty alcohol derivative, in this case, said carbonate b) can be a mono or multifunctional aliphatic chain to cyclic carbonates with 2 carbon atoms of the carbonate ring of said carbonate compound b) forming an integral part of said chain. As already described, said carbonate b) can also be obtained by the reaction of dimethylcarbonate with an aliphatic or cycloaliphatic polyol of functionality of at least 2, preferably ranging from 2 to 6. According to a particular option, said carbonate cycle is substituted by said substituent R4 as defined above, which is optionally hydroxylated alkyl and optionally more particular R4 can form a ring attached to the carbonate ring by 2 common carbon atoms. According to a preferred variant of the invention, the cycle of cyclic carbonate b) is a 5-atom ring.
    [0007] The carbonate compounds b can also be obtained from a mono or polyepoxidized precursor, preferably polyepoxidized, bearing epoxy groups, modified in cyclic carbonates by adding carbon dioxide to said epoxy groups. As the epoxidized oligodiene, there may be mentioned an epoxidized oligobutadiene or epoxidized polyisoprene or oligomeric epoxidized butadiene and isoprene copolymers. As diolefin or epoxidized olefin, mention may be made of epoxidized dicyclopentadiene, epoxidized norbornene, epoxidized cyclohexene and epoxidized cyclohexadiene which are carbonates b) of cycloaliphatic structure. As epoxy compound precursor of a suitable carbonate as cyclic carbonate b) according to the invention, mention may also be made of epoxidized prepolymers obtained with excess of epoxide by amine-epoxide reaction or polyester epoxidized prepolymer by anhydride-epoxy reaction, acrylic oligomer and and / or epoxidized styrenic, in particular acrylic and / or styrene copolymer of glycidyl methacrylate or a polyepoxide monomer which is an ether or a glycidyl ester, in particular glycidyl ether derivatives of bisphenols, preferably hydrogenated or glycidyl ethers of aliphatic polyols or cycloaliphatic polyols or glycidyl esters of polyacids of initial functionality to carboxy before esterification. As polyepoxidized precursor compound, any epoxide of monomeric structure or of linear or branched oligomeric structure may be suitable, with in the case of oligomer preferably having a number-average molecular weight Mn of less than 1000 and preferably less than 600 Daltons and measured by GPC in polystyrene equivalents. More particularly, the epoxidized precursor compound of said carbonate b) according to the invention may be a diepoxide monomer and may be chosen from: ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, butanediol diglycidyl ether, neopentyl glycol diglycidyl ether, diglycidyl ether of hexanediol, diglycidyl ether of cyclohexane dimethanol, diglycidyl ether of bisphenol A (DGEBA) hydrogenated or non-hydrogenated, diglycidyl ether of bisphenol F (DGEBF) hydrogenated or non-hydrogenated, these compounds being optionally alkoxylated, for example with 1 to 4 alkoxy units such as ethoxy and / or propoxy or ortho-iso- or terephthalic acid diglycidyl ester, tetrahydrophthalic acid diglycidyl ester or hexahydrophthalic acid diglycidyl ester. Said mono- or polyepoxidized compound, in particular diepoxidized, may also be an epoxidized oligomer or an epoxidized resin such as epoxidized oils, in particular soya, epoxidized polybutadiene or a condensation or addition prepolymer bearing epoxy end groups (or epoxy) or oxiranes). The epoxy functionality of this epoxidized compound should correspond to the functionality m of cyclic carbonates of said carbonate b) referred to. For example, for a dicarbonate, i.e. having 2 cyclic carbonates, the epoxidized precursor is preferably a diepoxide also called diepoxy.
    [0008] Said carbonate b) for m = 2 may alternatively be the product of the reaction of dimethylcarbonate with an aliphatic or cycloaliphatic polyol of functionality of at least 2, preferably ranging from 2 to 6, with formation of said cyclic carbonates compounds b) as defined according to the invention. Said compound d) is a multifunctional acrylate, insofar as it carries at least one acrylate group, one acrylate being the minimum if the other group is a methacrylate and at least two acrylates in the absence of any methacrylate group with a minimum of two acrylates in this case. This minimum of starting functionality of said compound d) is that required when a monofunctional urethane oligomer is targeted in acrylate or methacrylate starting from a carbonate compound b) monofunctional and a polyamine a) bifunctional (n = 2). It should be noted that the reaction between an amine group, whether primary or secondary, and a carbonate group always gives a urethane group, with the only difference, in the case of a group of secondary amine by relative to the primary amine, that the nitrogen atom of the urethane group is substituted (if secondary amine) instead of carrying a hydrogen (if primary amine). On the other hand, the two residual groups -NH- of a primary amine group after the formation of the m urethane groups can react with two acrylate groups on two different molecules of compound d). Said compound d) can be represented generally by R5- (O2CCH = CH2) (- 02CC (R6) = C1-12) p with R5 being a hydrocarbon residue of valence p + 1 and R6 is H or methyl for a part or the all of the groups and preferably R5 is a polyol residue selected from alkoxylated and / or substituted alkylene polyol optionally, optionally substituted cycloalkylene polyol or aralkylene polyol optionally alkoxylated and / or substituted on the aromatic ring or polyether polyol or polyester polyol or R5 is a residue of a multifunctional epoxy acrylate compound bearing an acrylate group and additional acrylate and / or methacrylate moieties. Said compound d) is according to a first option a multifunctional acrylic monomer having a functionality of at least 2, in particular greater than 2 and up to p + 1 equal to 6 and selected from: dl) acrylate esters of alkoxylated polyols or non-alkoxylated, preferably polyols selected from the group: trimethylol propane, ditrimethylol propane, pentaerythritol, dipentaerythritol, diethylene glycol, dipropylene glycol, tripropylene glycol, glycerol, propylene glycol, butane diol, hexane diol or d2) epoxy acrylates, d3) aminoacrylates. According to a second option, said compound d) is a multifunctional acrylic oligomer having a functionality of at least 2, in particular greater than 2 and up to p + 1 equal to 12 and selected from: d4) acrylated acrylic oligomer which can be a copolymer of acrylated glycidyl methacrylate or acrylated styrene oligomer which may be a copolymer of styrene with maleic anhydride or acrylic acid which is acrylated with hydroxy ethyl acrylate, d5) acrylated hydroxyl oligomer, in particular from acrylated hydroxyl polydienes , preferably acrylated polybutadiene hydroxyl and more preferably hydrogenated hydrogenated hydroxylated polybutadiene, d6) acrylated epoxidized oil, d7) acrylated epoxidized oligodiene, d8) oligoether acrylates, d9) acrylate oligoesters, dl 0) oligoaminoacrylates.
    [0009] The term "acrylates" according to these options below means that the compound d) can carry only acrylate groups -OC-CH = CH2 or it can carry at least one acrylate and groups of which a part or all are groups methacrylates according to -O 2 C-C (CH 3) = CH 2. According to a particular option, d) bears only acrylate groups (without methacrylate), which gives a higher reactivity to the corresponding oligomer according to the invention. According to a particular preference of said oligomer according to the invention, said polyamine a) is a diamine. More specifically, said polyamine a) may be a diamine selected from the secondary-primary, primary-primary or secondary-secondary diamines, preferably secondary-primary or secondary-secondary diamines.
    [0010] According to a more particular option, said diamine is selected from the secondary-primary diamines, preferably from: N-methyl-1,3-propane diamine, N-methyl-ethyl-diamine, N-methyl-1,4-butane-diamine, N-methyl-1, 5- pentane diamine. According to another more particular option, said diamine is selected from secondary-secondary diamines, preferably from: N-methyl-methyl-1,3-propane diamine, N-methyl-methyl-ethyl-diamine, N-methyl, N ' methyl 1,4-butane diamine, N-methyl, N'-methyl 1,5-pentanediamine. According to a particularly preferred option of the oligomer of the invention, the carbonate cycle of said carbonate b) is 5 atoms, said polyamine a) is a secondary-primary diamine with n1 = 0 and R = H as defined according to formula al) as defined above and said oligomer comprises at least one oligomer of the following general formula (I): RC 1-12 = CH (R6) -OO2) p-R5-02C-CF-12-CF12-N (R1) R2-N FI-OO2-C (R4) -CH (O1) 1p R3 (I) with R1 being as defined above in formula a1) R2 being as defined above in formula al) R3 being as defined for compound b), the radical of valence m, carrying said m cyclic carbonates groups R4 being said optional substituent of the carbonate ring as defined above R5 being as defined for said compound d) above R6 being H or methyl or H and methyl if p is other than 1. According to another option, said carbonate cycle of said carbonate b) is 6 atoms, said polyamine a) is a e secondary-primary diamine with n1 = 0 and R = H as defined according to formula al) above and said oligomer comprises at least one oligomer of the following general formula (II): RCH2 = CH (R6) -OO2) p-R5 -O2C-CH2-CH2-N (R1) -R2-NH-OO2-C (R4) -CH2CH (OH) -L, R3 (II) with R1, R2, R3, R4, R5 and R6 being such that defined above in formula (I). More particularly, the functionality of the acrylate and / or methacrylate groups of said urethane oligomer according to the present invention may vary from 1 to 30, preferably from 2 to 20, more particularly from 3 to 20.
    [0011] According to a particular and preferred case of oligomer as defined according to the invention, p varies from 1 to 11, preferably from 2 to 11, more preferably from 2 to 5, still more preferably being greater than 2 and up to 5. According to a more particular case for this oligomer of the invention, m = 2 and p varies from 2 to 11 and preferably p varies from 3 to 5.
    [0012] Said oligomer has a linear or branched structure. By definition, it can not include a crosslinked structure, which is thus excluded. Those skilled in the art know in particular to choose the proportions and functionalities of reactive components and the conversion rate of the reactive functions in order to avoid any crosslinking or chemical gelling of the reagent system. This question can only arise when one of the reactive components a) or b) or a) and b) first in the reaction of the first step is of greater than 2 functionality, ie when a branched structure is targeted. In this case, it is possible to control the structure without any possible crosslinking by adjusting the proportions of the reagents so that the number average functionality (per mole of reactant component) on all of the reactive components (a) + b)) does not exceed 2 or if it exceeds 2 to limit the conversion rate well before the predictable gel point (gelling), either by experimentation or by calculation according to the Macosko-Miller relationship and / or by progressive addition of component the least functionalized on the most functionalized component with effective stirring (maintained in excess of reactive functions by the gradual addition of the second reactive component). The Macosko-Miller relationship cited above is as defined by Macromolecules, vol. 9, pp. 199-211 (1976) and is considered well known to those skilled in the art. For clarity, we recall below this relation which links the critical ratio of the reactive functions for two reactive components A and B (respectively a) and b) in our case) at the critical point of gel I-, = (reactive functions of A) / (reactive functions of B), with the following relation linking the average functionality fA of A, fB of B and the critical conversion rate xg at the gel point: - 13 - rc * x2 = 1 / Rf B - 1) * (fA-1)] The objective is to adjust the ratio r = (reactive functions of A) / (reactive functions of B) so that it does not exceed a critical value for xg close to 1 ( total conversion of functions in default).
    [0013] Then, the same relation is to be respected for the reaction of modification of said intermediate compound c) with said compound d), bearing an acrylate and p acrylates and / or methacrylates, respectively replacing the functionalities fA and fB by those of c ) and d). It is obvious that in the case where a single acrylate group is present in compound d) the risk of gelation does not exist by amine-acrylate reaction because the methacrylate groups are not reactive by addition of Michael. Therefore, the relation is to be considered in the case where at least two acrylates are present in d) and the functionality of the polyamine a) is at least 3 in -N H-. It should be noted here that in the functionality of c) in reactive groups, -NH-, is two for each primary amine reactive residual group and one for each secondary amine reactive residue group. Therefore, both the proportions and functionalities of a) and b) in the first reaction step of formation of urethane-amines per molecule of said compound c) as the proportions and functionalities of said compound c) (residual reactive groups - N H-) and said compound d) (acrylate) in the second reaction step (formation of aminoacrylate by addition of -NH- on acrylate d) respect in each of said two steps, said relationship adapted (applied) to each said steps. With regard to its functionality in acrylates and / or methacrylates, said oligomer according to the present invention may have a functionality f in acrylate or methacrylate groups, which may vary from 1 to 30, with f = 1 if monofunctional, preferably multifunctional oligomer of functionality f from 2 to 20, more particularly from 3 to 20. More particularly, concerning p which characterizes the number of acrylate and / or methacrylate functions carried by carbon-nitrogen bond (imine) formed by the addition of Michael, this parameter p may vary from 1 at 10, in particular p = 10 with multiacrylated oligomers preferably of 1 to 5, in particular p = 5 with MFA monomers such as dipentaerythritol as compound d) as defined according to the invention. In fact, the carbon-nitrogen (imine) bond formed by said Michael addition in the second step corresponds to a group -N-CH2-CH2-OO2-R5 (-O2C-CH = CH-R6) p with R6 being H or methyl or H and methyl if p different from 1, which group is an aminoacrylate bearing acrylate groups and / or methacrylates. According to a more preferred particular case, said oligomer according to the invention corresponds to m = 2 and p = 2 to 10, preferably p = 3 to 5. According to a particular option of said oligomer according to the invention, the number of residual amine -NH- reactive groups of said intermediate product c) is equal to the number of moles of said compound d). According to another particular option of said oligomer according to the invention, said compound d) is in molar excess relative to the amine -NH- reactive residual groups of said intermediate product c) and thus said residual compound d) is present in said oligomer as reactive diluent .
    [0014] The molar excess of d) means that there is more than one mole of compound d) per residual amine reactive group -NH- of said product c). The level of compound d) residual corresponds to this molar excess (difference in moles of d)) with respect to said reactive amine groups -NH-, which excess by definition could not react with c). According to an alternative definition of the oligomer of the invention with respect to its structure, it is a urethane oligomer of linear or branched structure, bearing one or more acrylate groups and / or methacrylates, in particular carrier of at least two acrylate and / or methacrylate groups and more particularly carrying more than two acrylate and / or methacrylate groups, said oligomer being characterized in that it comprises at least one oligomer of structure according to general formula (III) below: (Acr) p-R 5 -O-CH 2 -CH 2 - (R 7) NAU-R 3 [-U-A + N (R 7) -CH 2 -CH 2 -O 2 -R 5 - (Acr) 1 with acrylate group or methacrylate R5: residue of a compound d) bearing an acrylate group and additional acrylate and / or methacrylate groups, with p being equal to at least 1, in particular with d) and R5 being defined as described above according to the invention. 'A': polyamine residue as defined according to a) as described above according to the invention, carrier of n secondary or primary amine groups, with n ranging from 2 to 5, R3: carbonate residue b) carrier of m cyclic carbonate groups with 5 or 6 atoms, with m ranging from 1 to 2, optionally said residue being hydroxyl and / or said carbonate ring being substituted, in particular with b) and R3 being defined as described above according to the invention C1-C3 alkyl or cycloalkyl, if secondary amine or R7: -CH2-CH2-OO2-R5- (AC0p, if primary amine, rAcr ': acrylate or methacrylate or acrylate + methacrylate-U mixture: urethane linkage formed by cyclic carbonate reaction with secondary amine (-NH-) or primary (-NH2), with an OH in the beta or gamma position as a function of the number of atoms of the carbonate ring at respectively 5 or 6 atoms. The invention relates to a process for the preparation of said oligomer as defined above. the present invention, which process comprises the following steps: i) reaction between said polyamine a) and said carbonate compound b) carrying cyclic m carbonates, with a) and b) being as defined above according to the invention, said polyamine being in stoichiometric excess with respect to b) and being added progressively to said carbonate b) initially present in the reactor and said reaction giving an intermediate product c) carrying m urethane groups and alpha or beta hydroxyl groups; urethane and carrier of amine residual groups -NH- ii) modification reaction of said compound c), by adding each of said amine reactive residual groups of said product c) to an acrylate group of a compound d) bearing in addition to said acrylate group, of additional acrylate and / or methacrylate groups, with each amine -NH- reactive residue group of said product c) thus being converted into a carbon-nitrogen bond bearing said acrylate and / or methacrylate groups and thus obtaining said urethane oligomer, with said polyamine a) bearing n primary and / or secondary amine groups and optionally at least one tertiary amine group, with n ranging from 2 to 5, preferably from 2 to 4 and more preferably from 2 to 3, even more preferably from 2, said carbonate b) carrying m carbonate groups with m ranging from 1 to 2, preferably the cycle of said cyclic carbonate groups being a 5- or 6-membered ring, said intermediate product c) carrying m urethane groups and alpha or beta hydroxyl groups of said urethane and m * (n-1) to m * (2n- 2) amine -NH- reactive residual groups, said compound d) bearing acrylate and / or methacrylate groups in addition to said acrylate group which reacts with one of said amine -NH- reactive residual groups with p being at least 1 and preferably at least 2 and the number of said reactive amine -NH-reactive groups being less than or equal to the number of moles of said compound d), each carbon-nitrogen bond formed having acrylate and / or methacrylate moieties and said urethane oligomer having acrylate and / or methacrylate functionality ranging from m * p (n-1) to m * p (2n-2). More particularly, the reaction of step i) can be carried out at a temperature ranging from 20 to 80 ° C, preferably from 45 to 65 ° C and that of step ii) from 80 to 95 ° C, preferably from 80 to 90 ° C. The present invention also relates to said intermediate product c) which is a hydroxyl multi-urethane-amine, as defined above as product of the first reaction step i) as described in the definition of the oligomer urethane product of the invention or process for preparing said oligomer according to the present invention. More particularly, said product is the intermediate product c) of reaction i) between said polyamine a) as defined above and said carbonate b), as defined above, or the same product c) as obtained from the end of step i) of the process for preparing said oligomer according to the invention. Another subject of the invention relates to a crosslinkable composition, which composition comprises as binder at least one oligomer as defined above or as obtained by a process as defined above according to the invention. More particularly, said composition is crosslinkable by radiation and / or by thermal peroxide or at low temperature and / or Michael type addition, particularly in the case of oligomers carrying at least two acrylate functions and / or by another dual route which may involve at least two of the aforementioned routes and / or all or part of the residual hydroxyl moieties of said oligomer by reaction thereof with a crosslinking agent reactive with said hydroxyl. Said hydroxyls are secondary and in the beta or gamma position of the urethane bond formed by reaction between cyclic carbonate function and beta or gamma-dependent amine function of the number (respectively 5 or 6) of atoms of the carbonate ring of b). In particular, the secondary hydroxyl is in the beta position (5-atom ring for b). Suitable such agents include dianhydrides or melamine, in particular dianhydrides. With respect to its potential use, said crosslinkable composition of the invention may be a coating composition, preferably coatings among paints, varnishes and inks, a molding composition, a sealant or chemical sealant composition, a adhesive composition; a composition for layer-by-layer 3D object-making systems; a composition for 3D printing systems; a concrete composition or a composite composition. Another subject of the invention relates to the use of an oligomer as defined above according to the invention or obtained by the method of the invention described above, said oligomer being used as a reactive binder in the compositions of coatings, in this case including paints, varnishes and inks or composition of adhesives, molding, sealing agent, chemical sealing, layer-by-layer 3D object making systems, printing systems 3D, concrete or composite. Finally, the present invention also covers the finished product, which results from the use of at least one oligomer as defined according to the invention or obtained by the process of the invention described above, preferably a product chosen from the coatings, in particular coatings for paints, varnishes and inks or produced from adhesive joints, molded parts, 3D objects obtained layer by layer, 3D printing, gaskets, chemical sealing, finished concrete or composite articles. The following examples are given by way of illustration of the invention and its performance and in no way limit its coverage. Experimental part 1) Preparation of oligomers according to the invention Example 1 161.55 g of propylene carbonate (Huntstman Jeffsol, Mw of 102 g / mol), 0.81 g of trisnonylphenylphosphite and 1 g of propylene carbonate are introduced into a reactor 11 g 2,6-di-tert-butyl-4-methylphenol (BHT). Under stirring and bubbling with nitrogen, 146.80 g of N-methyl-1,3-propane diamine (Aldrich, Mw of 88.15 g / mol) are added over one hour at a constant rate. An exotherm of about 30 ° C is observed. At the end of the addition, the temperature of the mixture is raised to 60 ° C. After one hour at 60 ° C., under bubbling with air, 689.85 g of tripropylene glycol diacrylate (TPGDA, Sartomer 5R306, Mw of 300 g / mol) are added to the mixture in fifteen minutes at a constant rate. At the end of the addition, the temperature of the mixture is raised to 85-90 ° C. The progress of the reaction is monitored by measuring the total amine and tertiary amine indices. The reaction is stopped when the tertiary amine index = total amine number. EXAMPLE 2 162.93 g of propylene carbonate (Huntstman Jeffsol, Mw of 102 g / mol), 0.81 g of trisnonylphenylphosphite and 1 g of 2,6-di-tert are introduced into a reactor of 11_. -butyl-4-methylphenol (BHT). Under stirring and bubbling with nitrogen, 147.81 g of N-methyl-1,3-propane diamine (Aldrich, Mw of 88.15 g / mol) are added over one hour at a constant rate. An exotherm of about 30 ° C is observed. At the end of the addition, the temperature of the mixture is raised to 60 ° C. After one hour at 60 ° C., while bubbling with air, 687.44 g of trimethylolpropane triacrylate (TMPTA, Sartomer 5R351, Mw of 296 g / mol) are added to the mixture in fifteen minutes at a constant rate. At the end of the addition, the temperature of the mixture is raised to 85-90 ° C. The progress of the reaction is monitored by measuring the total amine and tertiary amine indices. The reaction is stopped when the tertiary amine index = total amine number.
    [0015] EXAMPLE 3 336.04 g of Polyethylene oxide dicarbonate (Specific Polymers, Mw of 632.5 g / mol), 1.68 g of trisnonylphenylphosphite and 2.07 g of 2,6-di are introduced into a 1 L reactor. -tert-butyl-4-methylphenol (BHT). Under stirring and bubbling with nitrogen, 95.38 g of N-methyl-1,3-propane diamine (Aldrich, Mw 88.15 g / mol) are added over one hour at a constant rate. An exotherm of about 30 ° C is observed. At the end of the addition, the temperature of the mixture is raised to 60 ° C. After one hour at 60 ° C., while bubbling with air, 564.84 g of trimethylolpropane triacrylate (TMPTA, Sartomer 5R351, Mw of 296 g / mol) are added to the mixture in fifteen minutes at a constant rate. At the end of the addition, the temperature of the mixture is raised to 85-90 ° C.
    [0016] The progress of the reaction is monitored by measuring the total amine and tertiary amine indices. The reaction is stopped when the tertiary amine index = total amine number. 2) Characteristics of the prepared products Characteristics Unit Example 1 Example 2 Example 3 Viscosity Noury Pa.s 2.0 (25 ° C.) 2.4 (50 ° C.) 12.3 (50 ° C.) Crosslinking speed under UV lamp m / min <10 50> 80 - 19 - Number Persoz hardness of oscillations 60 75 103 Flexibility mm N / DA 20 8 Resistance to acetone s 10> 300> 300 Application properties are measured on a crosslinked film under UV lamp « melting 120 VV / cm from an urethane amino-acrylate mixture according to the invention / Darocur® 1173 photoinitiator in the proportions 96/4 w / w.
    [0017] Methods used Determination of reactivity (speed of crosslinking): The mixture is applied in a 12 μm film on a contrast card ("Penoparc charts form 1B" Leneta), then is crosslinked using a Hg 120 fusion lamp. VV / cm. The minimum required passage rate (in m / min) is measured to obtain a dry film to the touch.
    [0018] For the following tests of hardness, flexibility and resistance to acetone, the photocured films are left in the air conditioned room (T = 23 ° C) for 24 hours after crosslinking and before the measurements. Determination of Persoz hardness: The mixture is applied in 100 μm film to a glass plate and crosslinked by a 120 VV / cm Hg fusion lamp at a speed of 8 m / min. The number of oscillations before oscillation damping (passage from 12 ° to 4 ° amplitude), a pendulum in contact with the coated glass plate according to ISO 1522 is measured.
    [0019] Determination of flexibility: The mixture is applied in 100 μm film on a 25/100 mm thick smooth plate (D-46 Q-Panel), then cross-linked by a 120 VV / cm Hg fusion lamp at a speed 8m / min. The coated plate is bent on cylindrical mandrels according to ISO 1519. The result is expressed as the value (in mm) of the smallest radius of curvature that can be applied to the coating without it cracking or takes off from the support. Determination of resistance to acetone: The mixture is applied in 12 μm film to a glass plate and then crosslinked by a 120 VV / cm Hg fusion lamp at a speed of 8 m / min. The coating is rubbed with a cloth soaked with acetone. The result is the time (expressed in seconds) beyond which the film comes off and / or disintegrates.
    权利要求:
    Claims (28)
    [0001]
    REVENDICATIONS1. Monofunctional or multifunctional urethane oligomer in acrylates and / or methacrylates, preferably acrylates, which can be obtained from the reaction of a specific polyamine a) with a cyclic carbonate compound b) bearing cyclic carbonic groups, said polyamine being in stoichiometric excess with respect to b) and said reaction giving an intermediate product c) bearing urethane moieties formed bearing amine -NH- reactive residual groups and then by an addition reaction of each of said amine reactive residual groups of said product c) on an acrylate group of a compound d) bearing, in addition to said acrylate group, additional acrylate and / or methacrylate groups, with each amine -NH- reactive residual group of said product c) thus being converted into a carbon-nitrogen bond carrier of said acrylate and / or methacrylate groups and thereby obtaining said ol urethane oligomer, with: said polyamine a) bearing n primary and / or secondary amine groups and optionally at least one tertiary amine group, with n ranging from 2 to 5, preferably from 2 to 4 and more preferably from 2 to 3, even more preferably from 2, - said carbonate b) bearing cyclic carbonyl groups with m ranging from 1 to 2, preferably the ring of said cyclic carbonyl groups being a 5- or 6-membered ring, said intermediate product c) carrying m urethane groups and m OH groups in alpha or beta of said urethane group and c) carrying m * (n-1) to m * (2n-2) amine -NH reactive residual groups said compound d) bearing acrylate and / or methacrylate groups in addition to said acrylate group which reacts with one of said amine -NH- reactive residual groups with p being at least 1 and preferably at least 2; and - l e number of said amine -NH- reactive residual groups of said product c) being less than or equal to the number of moles of said compound d), each carbon-nitrogen bond formed being carrying acrylate and / or methacrylate groups and said urethane oligomer carrying of m urethane groups and alpha or beta hydroxyl groups of said urethane and having a functionality in acrylates and / or methacrylates ranging from m * p (n-1) to m * p (2 n-2).
    [0002]
    2. Oligomer according to claim 1, characterized in that said n primary and / or secondary amine groups of said polyamine a) may be borne by a radical A of valence n, which radical A may be or comprise an aliphatic, cycloaliphatic or in the latter case, the said n amino groups being carried by at least one alkylene group attached to the aromatic ring and the rings of the said cyclic carbon m groups of the said carbonate b) are at 5 or 6 atoms and borne by a radical R3 of valence m, with R3 being a hydrocarbon radical of aliphatic, cycloaliphatic or aromatic structure and optionally hydroxyl or R3 may be a simple hydrogen for m = 1, optionally the carbonate ring may be substituted by a substituent R4 hydrocarbon optionally hydroxyl, R4 may be of structure aliphatic, cycloaliphatic or aromatic identical or different from that of R3 and possibly may form r a cycle attached to the carbonate ring by two common carbon atoms.
    [0003]
    3. Oligomer according to claim 1 or 2, characterized in that said polyamine a) is chosen from: - an alkylene polyamine at 02 to 054, said alkylene being 02 to 054 linear or branched and bearing said n primary amine groups and / or secondary, - a polyamine comprising at least two repeating units of: alkylene imine at 02 to 04, in particular ethylene imine or propylene imine, preferably ethylene imine, said polyamine a) being in this case an oligoalkylene imine polyamine, in particular a polyethylene imine polyamine including dendritic structure, - a polyamine comprising one or more units among: ether, ester-amide, amide, with in the case of the presence of several units, said polyamine a) being chosen from: oligoethers polyamines, oligoester amide -polyamines or multiester amide-polyamines.
    [0004]
    4. Oligomer according to one of claims 1 to 3, characterized in that said polyamine a) is chosen from the polyamines of formulas al) or a2): a) R1-NH-R2- (NH-R) (NH) -R11 with n1 being equal to 3, 2, 1 or 0 and preferably n1 being equal to 2, 1 or 0 a2) R1-NH- (R'2NH), 2-R "2 -NH-R 'with n2 being equal to 3, 2 or 1 with R 1 and R and R 'being independently selected from: H, alkyl preferably Cl-03, optionally said alkyl being alkoxylated or a cyclolalkyl, with R 1 being the same or different from R and R and with R and R 'being the same or different and in particular with R and / or R' being different from H, R2 being alkylene or cycloalkylene (including an aliphatic ring at 06) or aralkylene of valence n ranging from 2 to 5, with R2 being able to carry or comprise at least one tertiary amine group and R'2 and R "2 may be identical or different and selected from alkylene, preferably from 02 to Cg, more preferably only in R 2 in this case R "2 may carry or include at least one tertiary amine group.
    [0005]
    5. Oligomer according to one of claims 1 to 4, characterized in that said carbonate b) is a complete or partial ester of a polyamide, monomeric or oligomeric such as a oligoester polyacid, with a hydroxyl carbonate, preferably the glycerol carbonate or b) is a complete or partial ether of a monomeric or oligomeric polyol such as oligoester or oligoether polyol with a hydroxylated carbonate, preferably glycerol carbonate or b) is a complete or partial ether of a phenolic derivative , including bisphenol A or dihydroxy-phenylene with a hydroxyl carbonate, preferably glycerol carbonate or b) is an allylic or vinyl alcohol ether with a hydroxyl carbonate, preferably glycerol carbonate or a methacrylate of a carbonate hydroxyl, preferably glycerol carbonate or b) is a carbonate obtained by adding CO 2 to an epoxidized monomeric or oligomeric precursor compound or b) is the pro the reaction of dimethylcarbonate with an aliphatic or cycloaliphatic polyol having a functionality of at least 2, preferably from 2 to
    [0006]
    6. The oligomer according to one of claims 1 to 5, characterized in that said compound d) is represented overall by R6- (O2CCH = CH2) (- 02CC (R6) = CH2) p with R5 being a hydrocarbon residue of valence p + 1 and R6 is H or methyl for some or all of the groups, and preferably R5 being a polyol residue selected from: alkylene polyol optionally substituted and / or substituted, optionally substituted cycloalkylene polyol or aralkylene polyol optionally alkoxylated and / or substituted on the aromatic ring or polyether polyol or polyester polyol or R5 is a residue of a multifunctional epoxy acrylate compound carrying an acrylate group and additional groups acrylates and / or methacrylates.
    [0007]
    7. Oligomer according to one of claims 1 to 6, characterized in that said polyamine a) is a diamine.
    [0008]
    8. Oligomer according to one of claims 4 to 7, characterized in that the carbonate ring of said carbonate b) is 5 atoms, said polyamine a) is a secondary-primary diamine according to formula al) defined according to claim 4, with n1 = 0 and R = - 23 - H and said oligomer comprises at least one oligomer of the following general formula (I): RCH2 = CH (R6) -OO2) p-R5-02C-C1-12-CH2-N (R1) -R2-NH-OO2-C (R4) -CH (OH) -], R3 (I) with R1 being as defined in claim 4 R2 being as defined in claim 4 R3 being such as defined in claim 2 wherein R4 is as defined in claim 2, wherein R5 is as defined in claim 7, wherein R6 is H or methyl or H and methyl if p is not 1.
    [0009]
    9. Oligomer according to one of claims 4 to 7, characterized in that said carbonate cycle of said carbonate b) is 6 atoms, said polyamine a) is a secondary-primary diamine according to formula al) as defined in claim 4 with n1 = 0 and R = H and said oligomer comprises at least one oligomer of the following general formula (II): RCH2 = CH (R6) -OO2) p-R5-02C-CH2-CH2-N (R1) - R2-NH-OO2-C (R4) -CH2CH (OH) -1mR3 (II) with R1, R2, R3, R4, R5 and R6 being as defined according to claim 8.
    [0010]
    10. Oligomer according to one of claims 1 to 7, characterized in that said polyamine a) is a diamine selected from the diamines secondary-primary, primary-primary or secondary-secondary, preferably secondary-primary or secondary-secondary .
    [0011]
    11. Oligomer according to claim 10, characterized in that said diamine is selected from the secondary-primary diamines, preferably from: N-methyl-3-propane diamine, N-methylethane diamine, N-methyl-1,4- butane diamine, N-methyl-5-pentanediamine.
    [0012]
    12. Oligomer according to claim 10, characterized in that said diamine is selected from secondary-secondary diamines, preferably from: N-methyl-methyl-1,3-propane diamine, N-methyl-methyl-ethyl-diamine, N methyl, N'-methyl 1,4-butane diamine, N-methyl, N'-methyl 1,5-pentanediamine. 30
    [0013]
    13. Oligomer according to one of claims 4 to 7, characterized in that said polyamine a) is an amine according to formula a2) as defined in claim 4, with n2 = 1 and R1 and R 'being H and R' 2 and R "2 being identical or different alkylene and O 2 to O 6, in particular O 2 to O 4, more particularly said amine a 2) being selected from 3 (2-aminoethyl) aminopropylamine or bis (3-aminopropyl) amine.
    [0014]
    14. Oligomer according to one of claims 4 to 7, characterized in that said polyamine a) is an amine according to formula a2) as defined according to claim 4, with n2 = 2 or 3 and R1 and R ' being H and R'2 and R "2 being identical C2-C4, in particular C2-C3 alkylenes, more particularly said amine a2) being selected from triethylenetetramine or tetraethylenepentamine.
    [0015]
    15. Oligomer according to one of claims 1 to 14, characterized in that said compound d) is a multifunctional acrylic monomer having a functionality of at least 2, in particular greater than 2 and up to p + 1 equal to 6 and selected from: dl) acrylate esters of alkoxylated or non-alkoxylated polyols, preferably polyols selected from the group: trimethylol propane, ditrimethylol propane, pentaerythritol, dipentaerythritol, diethylene glycol, dipropylene glycol, tripropylene glycol, glycerol, propylene glycol, butane diol, hexane diol or d2) epoxy acrylates, d3) aminoacrylates.
    [0016]
    16. Oligomer according to one of claims 1 to 14, characterized in that said compound d) is a multifunctional acrylic oligomer having a functionality of at least 2, in particular greater than 2 and up to p + 1 equal at 12 and selected from: d4) acrylated acrylic oligomer which may be a copolymer of acrylated glycidyl methacrylate or styrene acrylated oligomer which may be a copolymer of styrene with maleic anhydride or acrylic acid which is acrylated with hydroxy ethyl acrylate d5) acrylated hydroxyl oligomer, in particular from hydroxylated acrylated polydienes, preferably hydroxylated acrylated polybutadiene and more preferentially hydrogenated hydroxylated acrylated polybutadiene d6) acrylated epoxidized oil d7) acrylated epoxidized oligodiene d8) oligoether acrylates d9) acrylate oligoesters d 10 ) oligoaminoacrylates.
    [0017]
    17. Oligomer according to one of claims 1 to 16, characterized in that the functionality f in acrylate groups and / or methacrylates ranges from 1 to 30, with f = 1 if monofunctional, preferably multifunctional oligomer of functionality f ranging from 2 to 20, more particularly from 3 to 20.
    [0018]
    18. Oligomer according to one of claims 1 to 17, characterized in that p varies from 1 to 11, preferably from 2 to 11, more preferably from 2 to 5, still more preferably being greater than 2 and up to 5.
    [0019]
    19. Oligomer according to one of claims 1 to 18, characterized in that m = 2 and that p varies from 2 to 11 and preferably p varies from 3 to 5. -
    [0020]
    20. Oligomer according to one of claims 1 to 19, characterized in that said compound d) is in molar excess relative to the amino groups -NH- of said intermediate product c) and with said residual compound d) being present in said oligomer as a reactive diluent.
    [0021]
    21. Urethane oligomer of linear or branched structure, bearing one or more acrylate groups and / or methacrylates, in particular carrying at least two acrylate groups and / or methacrylates and more particularly carrying more than two acrylate groups and / or or methacrylates, said oligomer being characterized in that it comprises at least one oligomer of structure according to general formula (III) below: (Acr) p-R 5 -O 2 -CH 2 -CH 2-(R 7) NAU-R 3 A + N (R7) -CH2-CH2-OO2-R5- (Acr) 1 1 with rAcr ': acrylate or methacrylate group R5: residue of a compound d) bearing an acrylate group and additional groups acrylates and methacrylates, with p equal to at least 1, in particular with d) and R5 being as defined according to one of claims 1,6, 15 and 16, 'A': polyamine residue as defined according to a) in one of claims 1 to 4, 7 to 14 and 19, carrying n secondary or primary amine groups, with n ranging from 2 to 5, R3: carbonate residue b) bearing m cyclic carbonate groups with 5 or 6 atoms, with m ranging from 1 to 2, optionally said residue being hydroxyl and / or said carbonate ring being substituted, in particular with b) and R3 being as defined according to one of claims 1, 2, 5, 8, 9 and 19,: C1-C3 alkyl or cycloalkyl, if secondary amine or R7: -CH2-CH2-OO2-R5 - (AC0p, if primary amine, rAcr ': acrylate or methacrylate or acrylate + methacrylate mixture U: urethane bond formed by reaction cyclic carbonate-secondary amine (-NH-) or primary (-N H2), with an OH in beta position or gamma as a function of the number of atoms in the carbonate ring at 5 or 6 atoms, respectively.
    [0022]
    22. Process for the preparation of an oligomer as defined according to one of claims 1 to 20, characterized in that it comprises the following steps: i) reaction between said polyamine a) as defined according to one of the claims 1 to 4, 7 to 14 and 19 and said carbonate compound b) bearing cyclic m carbonates, as defined according to one of claims 1, 2, 5, 8, 9 and 19, said polyamine being in stoichiometric excess with respect to to b) and being added progressively to said carbonate b) initially present in the reactor and said reaction giving an intermediate product c) carrying m urethane groups and alpha or beta hydroxyl groups of said urethane and bearing groupings residual amine -NH- reagents ii) modification reaction of said compound c), by adding each of said amine reactive residual groups of said product c) to an acrylate group of a compound d) carrier in addition to said group acrylate, of acrylate and / or methacrylate additional groups as defined in one of claims 1, 6, 15 and 16, with each amine -NH- reactive residual group of said product c) thus being converted into a carbon-nitrogen bond carrier of said acrylate and / or methacrylate groups and thereby obtaining said urethane oligomer, with - said polyamine a) carrying n primary and / or secondary amine groups and optionally at least one tertiary amine group, with n ranging from 2 to 5, preferably from 2 to 4 and more preferably from 2 to 3, even more preferably from 2, - said carbonate b) carrying m carbonate groups with m ranging from 1 to 2, preferably the cycle of said cyclic carbonate groups being a ring with 5 or 6 atoms, - said intermediate product c) carrying m urethane groups and m hydroxyl groups in alpha or beta of said urethane and m * (n-1) to m * (2 n-2) amine -NH- residual groups, - said compound d) bearing acrylate and / or methacrylate groups in addition to said acrylate group which reacts with one of said amine -NH- reactive residual groups with p being at least equal to 1 and preferably at least 2 and the number of said amine -NH- reactive residual groups being less than or equal to the number of moles of said compound d), each carbon-nitrogen bond formed being carrying acrylate groups and / or methacrylates and said urethane oligomer having acrylate and / or methacrylate functionality ranging from m * p (n-1) to m * p (2n-2).
    [0023]
    23. Multi-urethane hydroxyl amine product, characterized in that it is the intermediate product c) of the reaction i) between said polyamine a) as defined according to one of claims 1 to 4, 7 to 14 and 19 and said carbonate b) as defined according to one of claims 1, 2, 5, 8, 9 and 19 or as obtained at the end of step i) of the method of preparation as defined in claim 22.- 27 -
    [0024]
    24. Crosslinkable composition, characterized in that it comprises as binder at least one oligomer as defined in one of claims 1 to 21 or as obtained by a process as defined according to claim 22.
    [0025]
    25. Crosslinkable composition according to claim 24, characterized in that it is crosslinkable by radiation and / or thermal peroxide or low temperature and / or Michael type addition in the case of oligomers bearing at least one at least two acrylate functions and / or by other dual route involving at least two of the cited routes and / or involving all or part of the residual hydroxyl m moieties of said oligomer, by reaction of the latter with a crosslinking agent reactive with said hydroxyls .
    [0026]
    26. Crosslinkable composition according to claim 24 or 25, characterized in that it is a coating composition, preferably among coatings for paints, varnishes and inks, a molding composition, a composition of sealant or sealant, an adhesive composition, a composition for layer-by-layer 3D object-making systems, a composition for 3D printing systems, a concrete composition or composite composition.
    [0027]
    27. Use of an oligomer as defined in one of claims 1 to 21 or obtained by the process as defined in claim 22, as a reactive binder in coating compositions, in particular paints, varnishes and inks, adhesives, molding, sealant, chemical sealing, for 3D layer-by-layer production systems for 3D printing systems, concrete or composite.
    [0028]
    28. Finished product, characterized in that it results from the use of at least one oligomer as defined according to one of claims 1 to 21 or obtained by the method as defined in claim 22, preferably produced selected from coatings, in particular coatings for paints, varnishes and inks, produced from adhesive joints, molded parts, 3D objects obtained layer by layer, 3D printing, gaskets, chemical sealing, finished concrete or composite articles.
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    同族专利:
    公开号 | 公开日
    TW201619237A|2016-06-01|
    US20170342024A1|2017-11-30|
    JP2017538798A|2017-12-28|
    CN106795281A|2017-05-31|
    TWI618731B|2018-03-21|
    JP6731914B2|2020-07-29|
    WO2016059340A1|2016-04-21|
    FR3027306B1|2018-04-06|
    EP3207078B1|2021-10-13|
    EP3207078A1|2017-08-23|
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    法律状态:
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    2016-04-22| PLSC| Publication of the preliminary search report|Effective date: 20160422 |
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    2021-09-13| PLFP| Fee payment|Year of fee payment: 8 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1459890A|FR3027306B1|2014-10-15|2014-10-15|MONO OR MULTIFUNCTIONAL URETHANE AMINO-ACRYLATE OLIGOMERS WITHOUT ISOCYANATE|FR1459890A| FR3027306B1|2014-10-15|2014-10-15|MONO OR MULTIFUNCTIONAL URETHANE AMINO-ACRYLATE OLIGOMERS WITHOUT ISOCYANATE|
    TW104132530A| TWI618731B|2014-10-15|2015-10-02|Isocyanate-free mono- or multifunctional amino-acrylate urethane oligomers|
    PCT/FR2015/052754| WO2016059340A1|2014-10-15|2015-10-13|Monofunctional or multifunctional urethane acrylate oligomers without isocyanate|
    EP15788172.3A| EP3207078B1|2014-10-15|2015-10-13|Non-isocyanate urethane mono- or multiacrylate oligomers|
    US15/519,365| US20170342024A1|2014-10-15|2015-10-13|Monofunctional or multifunctional urethane acrylate oligomers without isocyanates|
    CN201580055858.0A| CN106795281A|2014-10-15|2015-10-13|Simple function or polyfunctional urethane acrylate oligomer without isocyanates|
    JP2017520369A| JP6731914B2|2014-10-15|2015-10-13|Isocyanate-free monofunctional or polyfunctional urethane acrylate oligomer|
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