IONIC OLIGOMER AND POLYMERIZABLE COMPOSITION CONTAINING THE SAME FOR HYDRO-FRAGMENTABLE MATERIALS FO

专利摘要:
The present invention relates to an oligomer carrying at least one crosslinkable ethylenic unsaturation and at least one ionic bond which comprises in its structure at least one aminoacrylate group and at least one tertiary amine in salified form with at least one carboxylic acid. The invention also covers a preparation process, a solution of said oligomer in a reactive diluent, a crosslinkable composition comprising said oligomer, its use as a binder in crosslinkable compositions for materials with a temporary function and removable in water in coatings, hydrogels, 3D object printing and the crosslinked material that results from said oligomer.
公开号:FR3042195A1
申请号:FR1559638
申请日:2015-10-09
公开日:2017-04-14
发明作者:Guillaume Monnier；Christophe Duquenne；Sylvain Beaudrais
申请人:Arkema France SA；
IPC主号:

专利说明:

4) Evaluation des propriétés des compositions réticulés et des performances d’hydrofragmentation dans une solution aqueuse
Pour les tests de compression et d’hydro-fragmentation, les produits tels que décrits selon l’invention (Exemple 3 et 4) et les compositions comparatives (Exemple 5 et 6) sont formulés avec un taux global de photoinitiateur de 5% en poids composé de 4% d’Irgacur® 1173 (BASF) et de1% en poids de Lucirin® TPO-L (BASF) pour 95% en poids de composition testée du tableau 1. La réticulation est réalisée sous lampe UV 120 Watt/cm. Test de compression (suivant la norme N F EN ISO 604)
Type d’éprouvettes ; Cylindrique (diamètre: 13,3 mm, hauteur 26,5 mm) obtenues par réticulation sous lampe UV 120 Watt/cm d’une composition contenue dans un moule cylindrique en verre sacrifié ayant les dimensions (diamètre) correspondant à celles de l’éprouvette (longueur ajustée par découpage de l’objet réticulé).
Machine d’essai : INSTRON 1185 ReNew, cellule 10kN
Vitesse de l’essai : 1,3 mm/min.
Les éprouvettes ont été testées à 23°C
Les résultats sont présentés dans le tableau 2 ci-dessous.
Tableau 2
Test d’hvdro-fragmentation
Le test d’hydro-fragmentation est défini de la façon suivante :
Un objet réticulé en masse sous la forme d’un cylindre de 15 g et de 15 cm3 (2 cm de haut, 1,5 cm de rayon) est plongé pendant deux heures dans un bain contenant 400 ml d’une solution aqueuse d’hydrogénocarbonate de sodium (pH > 7) à 60°C, sous agitation magnétique (barreau magnétique). Après deux heures de traitement, le mélange est filtré et les solides résiduels séchés.
Deux critères sont alors mesurés et évalués : 1) Le poids du cylindre avant le test, puis après filtration et séchage, indique la partie de l’objet passée en solution, « hydrosoluble » ou « hydrodispersible » 2) L’aspect du cylindre après le test : une note de 0 à 5 est attribuée ; elle indique le degré « hydro-fragmentabilité » du matériau. a. 0 : le cylindre original est resté intact b. 5 : le cylindre est entièrement fragmenté, les résiduels solides se présentant sous forme de poudre homogène après filtration et séchage
Les objets cylindriques préparés pour le test sont obtenus à partir d’un moule en Téflon. 20 passages sous une lampe UV de 120 Watt/cm sont nécessaires pour obtenir l’objet réticulé. Les résultats sont présentés dans le tableau 3 ci-dessous.
Tableau 3
* : particules de taille homogène avec taille maximale inférieure à 7 mm ** : particules de taille homogène avec taille maximale inférieure à 5 mm *** : particules de taille très variable (très hétérogènes) de taille maximale majoritaire et supérieure à 20 mm
The present invention relates to a specific oligomer bearing at least one crosslinkable ethylenic unsaturation and at least one ionic linkage in the form of ammonium carboxylate, which oligomer comprises in its structure at least one aminoacrylate group and at least one tertiary amine y aminoacrylate, in salified form of ammonium carboxylate by at least one carboxylic acid compound. More particularly, the oligomer, object of the present invention, results from the association by ammonium carboxylate ionic bond between a precursor oligomer bearing said at least one aminoacrylate group and said carboxylic acid compound, which acidic compound may be a monoacid or a polyacid and in particular a polyacid which is a diacid, said acid compound being saturable or unsaturated and said precursor oligomer can carry ethylenic unsaturated polymerizable, in particular acrylate or may be without any ethylenic unsaturation with, in this case, The ethylenic unsaturation of the oligomer of the present invention is provided by said carboxylic acid compound. The oligomer according to the invention has as its main objective its use in applications concerning materials with a function or temporary use such as coatings or objects which can be easily removed after a temporary function, by simple cleaning with water or water saline or other aqueous solution, in particular having a pH> 7 and preferably> 8, more particularly by a jet of water and optionally at a suitable temperature and greater than the glass transition temperature of the crosslinked product obtained. A particular advantage sought for these coatings and articles or functional parts is that they are respectful of the health of operators and the environment in general without the use of dangerous solvents or corrosive products and which may affect health and the environment. More specific applications are also related to their high sensitivity to water and their ability to form gels in water (hydrogels) that can serve as a carrier of various active ingredients in aqueous medium and easily removed if necessary.
More particularly, the present invention relates to products crosslinked from said oligomers according to the invention, with crosslinked products which are hydro-fragmentable or water-soluble thus allowing their complete elimination by water or in aqueous medium as described above. In particular, this type of product has an interest in a crosslinkable composition to serve as a support material (also called sacrificial material) to pieces being elevated in the 3D printing technique, in particular according to the Inkjet 3D / polyjet technique with projection of crosslinkable composition (also known as resin) and firing under radiation, in particular UV layer after layer. Said carrier or sacrificial material is subsequently removed using a simple passage in a water bath with the pH and the bath temperature being adapted to the technique and the crosslinkable composition used. In some cases, it may be necessary to have agitation, or a soaking time and / or presence of additives for this elimination.
Before crosslinking under radiation and in particular under UV lamp, the crosslinkable composition comprising said crosslinkable oligomer must have a viscosity of less than 30 mPa.s at the ejection temperature of said composition which is typically greater than 45 ° C. During the manufacturing process, the sacrificial material must provide the expected characteristics of a support with essentially good mechanical strength to satisfy the function of "support" material and a minimum curing rate (crosslinking) under radiation, in particular UV . Preferably, the reactivity corresponds to a cooking rate (or crosslinking) equivalent to less than 1 passage at 10 m / min under a UV lamp of 120 Watt / cm for a 25 micron coating. Good dimensional stability with low shrinkage, preferably <1% can also be of interest.
At the end of the three-dimensional printing, the sacrificial material (support) must dissolve or be removed by hydro-fragmentation rapidly in water or an aqueous solution without leaving marks on the surface of the 3D object thus produced. The material for temporary use to be sacrificed is hydro-fragmentable according to the present invention if, after being placed in water or in an aqueous saline or basic solution (pH> 7) with magnetic stirring, the material disintegrates in the form of a "water-dispersible" fraction. Or "water-soluble" (passing into the aqueous phase after filtration on standard filter paper) and / or a residual solid fraction (after filtration) of homogeneous particle size and not exceeding 10 mm. More preferably, this disintegration results in two fractions as defined above. As a suitable test for characterizing the degree of hydro-fragmentability, the test as described in the experimental part of the description can be used.
The sacrificial support material surrounding the targeted 3D object has the temporary function of progressively supporting the shape of said article as the number of layers printed and crosslinked one by one progresses.
From the state of the art, the most common known solutions of crosslinkable compositions that can serve as "support" material for the 3 D object printed layer by layer are either based on inert material (non-reactive under radiation) and water-soluble or based on a polymerizable composition based on water soluble polymerizable monomers or water-soluble monoethylenic oligomers and comprising, as essential component, water-soluble inert oligomeric or polymeric components or other water-soluble additives making the "carrier" material removable by dissolution in the 'water.
For example, US 2013/0234370 discloses a water-soluble support material composition comprising a water-soluble monofunctional polymerizable monomer and a Mn polyoxypropylene glycol ranging from 100 to 5000 and / or water. US 2013/0337277 discloses a liquid composition for temporary self-destructible structures for a 3D printing process with said composition comprising a biodegradable copolymer by enzymatic degradation with activation of a biospecific enzyme after finishing the 3D object. The said copolymer may comprise polyethylene glycol, polyacrylic acid, polyhyaluronic acid, polycaprolactone or polyvinyl alcohol. US 2012/0178845 also discloses radiation crosslinkable compositions for 3D printing under radiation and, in particular, a composition suitable for supporting the 3D object having as reactive component an acrylic component or a vinyl ether-carrying component or a miscible component. water, which swells in water or in a basic or acid solution after crosslinking, said component may be an acrylated urethane oligomer based on polyethylene glycol or a partially acrylated polyol oligomer or an acrylated oligomer having hydrophilic substituents among amine, hydroxy or acid. A non-reactive component is also present selected from polyethylene glycol (PEG), methoxy PEG, glycerol, polyethoxylated polyol or propylene glycol. CA 2,239,439 relates to applications other than the printing of 3D objects and describes a process for producing aqueous paint that can be crosslinked under radiation, which paints are soluble in water and obtained by mixing a pre-paint A based on an oligomeric or polymeric binder bearing at least two ethylenic unsaturations which is immiscible with water, with a primary / tertiary amine B) at 0.2 to 5% by weight with respect to said pre-paint with incorporation of said amine in said oligomer or polymer, followed by neutralization of the amino groups with an acid and solubilization in water of the paint and adjustment of its viscosity. No mention of use of such a composition once cured as a temporary and temporary function material and in particular removable by water is described or taught. CA 2,239,310 discloses compositions similar to the previous case, aqueous paints, but starting from a compatible reactive binder, dispersible or soluble in water, and with increasing this compatibility (solubility) by modifying said binder with an amine and neutralization by an acid to improve the solubility of the paint binder before radiation curing. No. 5,792,827 describes aqueous compositions of coatings for wood or paper, crosslinkable under radiation and based on a multifunctional acrylate adduct with an amine. The amines can be neutralized with an acid such as lactic acid, acetic acid, formic acid or phosphoric acid. US 2012/0157351 discloses a method for inhibiting the formation of hydrated agglomerates in a fluid among water, gas and optionally a liquid hydrocarbon, comprising adding to said fluid an anti-caking additive or its salts. As additive products, dimethylpropylamine or dibutylpropylamine addition products are exemplified on 2-ethyl hexyl acrylate with salification of the tertiary amine by 1-chloro butane or acetic acid, respectively. No use in a polymerizable or crosslinkable composition and no use for materials with a temporary function is described or suggested.
None of the documents cited describes or teaches the principle of the present invention for obtaining materials with a temporary function and easily removable by water and as required, either as a support for printed objects in 3D layer by layer (under radiation), either as temporary coatings or as a temporary active agent vector, also removable with water and in particular the principle of a mixed crosslinked edifice with reversible ionic bonds and associating hydrophilic structures having a viscosity adapted to the application and sufficient mechanical strength to fulfill their function of use as temporary material removable water or a suitable aqueous solution.
In particular, the composition of the oligomer according to the invention or the polymerizable and in particular crosslinkable composition comprising it, more particularly leading by crosslinking to the 3D object support material, is free from any free component or water-soluble free additive and non-reactive by crosslinking as described in the state of the art cited above. The invention firstly relates to an oligomer which is ionic by carrying at least one ammonium carboxylate ionic linkage and being obtained from a precursor oligomer P comprising at least one aminoacrylate group and an acidic salifying compound by said ammonium carboxylate ionic linkage, at least one tertiary amine of said oligomer P, which may be an aminoacrylate or optionally another tertiary amine group (amine group or function having the same meaning for the following) carried by an amine compound forming said at least one aminoacrylate group. The invention also relates to said precursor oligomer P as an intermediate for preparing said oligomer as defined according to the present invention.
Also part of the invention, a solution of said oligomer in a reactive diluent and a polymerizable composition, in particular crosslinkable, comprising at least one oligomer as defined according to the invention.
Another subject of the invention relates to a process for the preparation of said oligomer comprising first the preparation of a precursor oligomer P and then its salification with a carboxylic acid compound in the form of ammonium carboxylate of at least one tertiary amine of said P oligomer, which may be at least one of said aminoacrylate groups and optionally at least one tertiary amine carried by the starting addition amine forming said aminoacrylate group.
Also part of the present invention, the use of said oligomer or its solution in a reactive diluent or a polymerizable composition, in particular crosslinkable comprising it or oligomer as obtained by the process described according to the invention (Γ use) as a polymerizable binder and more particularly crosslinkable for applications in water-removable, water-removable, or temporary use materials, aqueous saline solution or other aqueous solution which is basic, preferably for coatings, hydrogels or carrier material for 3D printing object layer by layer.
Finally, the present invention also covers the finished product polymer material, in particular crosslinked, obtained by polymerization (polymer) and in particular crosslinking (crosslinked product) of a composition comprising said ionic oligomer.
Thus, the first subject of the invention relates to a polymerizable oligomer which is in particular crosslinkable and carries at least one ethylenic unsaturation and at least one ammonium carboxylate ionic bond and which comprises in its structure or in its composition: ) at least one precursor oligomer carrying at least one tertiary amine function in the form of an aminoacrylate group, preferably at least two tertiary amine functions in the form of aminoacrylate groups, resulting from the addition of A) at least one compound amine according to A1) carrying at least one primary amine (-NH2) or / and secondary (-NH) function and optionally at least one tertiary amine and / or A2 function) bearing at least one amine function secondary (-NH) and optionally at least one tertiary amine function (with the amine compound according to A2) having no primary amine function-NH2), on B) at least one hydrophilic acrylate compound with thus forming said at least one a group aminoacrylate, and - C) at least one carboxylic acid compound attached to said precursor oligomer P by at least one ammonium carboxylate ionic bond with at least one of said aminoacrylate groups and optionally (with) at least one of said tertiary amine functions of said amine compound A), preferably said oligomer carrying at least two ionic carboxylate ammonium bonds as defined above.
The term "polymerizable" means "capable of polymerizing by the wearing of at least one polymerizable ethylenic unsaturation" and the term "crosslinkable" is a more specific case of the term "polymerizable" where said oligomer "may crosslink already alone and therefore carries at least 2 polymerizable ethylenic unsaturations per molecule ". It is obvious that said oligomer if it is "polymerizable" and "crosslinkable" alone is also and respectively "copolymerizable" and "crosslinkable" in a composition of monomers and / or other "polymerizable" or "crosslinkable" oligomers.
A "hydrophilic" acrylate means according to the present invention that said acrylate is soluble in water or water-dispersible in water without surfactant also said "self-dispersible" in water.
According to a first particular option in said oligomer of the invention, said amine compound A) can be selected from: - A1) an amine compound carrying at least one, in particular a primary amine function and optionally, from at least one, in particular a tertiary amine function and / or at least one, in particular a secondary amine function and / or - A2) an amine compound carrying at least one, in particular a secondary amine function and optionally at least one, in particular a tertiary amine function, and with said acrylate compound B) being at least one multifunctional acrylate compound according to B1) and / or monofunctional according to B2), and in particular in the case where A) is a compound according to A1) or comprises an amine compound according to A1), said acrylate compound B) is a mixture of at least one multifunctional acrylate according to B1) and at least one monofunctional acrylate according to B2).
More particularly, said hydrophilic acrylate compound B) is a mixture of multifunctional acrylate compound (hydrophilic) according to B1) and of acrylate compound (hydrophilic) monofunctional according to B2).
Said aminoacrylate group of the oligomer of the invention may carry at least one ethylenic unsaturation, in particular acrylate, or no ethylenic unsaturation and in the latter case said acid compound C) is ethylenically unsaturated.
According to a preferred option of said oligomer, said acid compound C) is a monoacid according to C1) which is ethylenically unsaturated according to C11) and said oligomer carries at least two ammonium carboxylate ionic bonds.
Different options exist for said carboxylic acid compound C). Firstly: - when said carboxylic acid compound C) is according to C1) a monoacid, in this case: C1) can be a monoacid according to C11) which is ethylenically unsaturated and at least one ethylenic unsaturation of said oligomer is carried by at least said monoacid according to C11) by ammonium carboxylate linkage with at least one of said tertiary amine functional groups from said aminoacrylate groups or optionally from the tertiary amine functions of said amine compound A), and optionally at least one other ethylenic unsaturation of said oligomer is carried by at least at least one aminoacrylate group in the form of aminoacrylate-terminal acrylate group of said precursor oligomer P, or C1) can be a monoacid according to C12) which is saturated and at least one ethylenic unsaturation of said oligomer, is carried by at least one aminoacrylate group in the form of aminoacrylate-terminal acrylate group of said precursor oligomer P, preferably said mo the acid according to C1) being, according to C11), an unsaturated monoacid, and - when said carboxylic acid compound C) is in accordance with C2) a polycarboxylic acid and preferably a diacid, in this case: C2) may be a polyacid according to C21) which is ethylenically unsaturated, in particular ethylenically unsaturated diacid, and at least one ethylenic unsaturation of said oligomer is carried by at least said polyacid according to C21) and optionally in addition, at least one ethylenic unsaturation is carried by at least one aminoacrylate group in the form of aminoacrylate groups terminal acrylate of said precursor oligomer P, or C2) may be a polyacid according to C22) saturated, in particular saturated diacid, and said precursor oligomer P carries at least one aminoacrylate-end acrylate group and said oligomer which results carries at least two ethylenic unsaturations acrylates.
Said "aminoacrylate" group corresponds to the linking group formed during the addition reaction of a "= NH" group of said amine compound A) to an acrylate group CH 2 = CH-CC> 2, with said aminoacrylate group represented by the following formula: "= N-CH2CH2-C02-" (1)
An "aminoacrylate-terminal acrylate" group means a residual acrylate group of a multifunctional acrylate according to B1), after formation of an "aminoacrylate" group as explained above with an acrylate group of an acrylate according to B1): (CH2 = CH-CO 2) nR of functionality n to acrylates of at least 2, according to the following scheme: = NH + (CH 2 = CH-CO 2) nR = N-CH 2 CH 2 -CO 2 -R (-O 2 C-CH = CH 2) n ( 2)
In the case above, for an addition = NH on an acrylate group there are n-1 acrylate groups carried by said "aminoacrylate" group and therefore, n-1 "aminoacrylate-terminal acrylate" groups.
According to a preferred option, said carboxylic acid compound C) in said oligomer according to the invention is an unsaturated diacid according to C21) or saturated according to C22) associating with two carboxylate ionic bonds, two molecules of said precursor oligomer P, by salification in the form of salt. ammonium carboxylate of one of said tertiary amine functional groups among said aminoacrylate groups formed or optionally among said tertiary amine functions of said amine compound A), on each of said molecules of said oligomer P, or said carboxylic acid compound C) is a monoacid according to C1), ethylenically unsaturated according to C11) having a polymerizable ethylenic unsaturation and said monoacid according to C11) salifies at least two of said tertiary amine functional groups in the form of (salt or ionic linkage of) ammonium carboxylate.
More particularly, in the case of a diacid according to C21) or according to C22) can be schematized said oligomer according to the invention with the following general formula (3): P (NH +) i [O2C-R'-C02-] m (ΉΝ), P (3) with R 'being ethylenically unsaturated if said acidic compound C) is according to C21) and R' being saturated if said acidic compound C) is according to C22). "I" being the number of ammonium carboxylate sites per molecule of precursor oligomer P and "m" the number of diacid molecules between two P precursor chains (molecules) with I = m.
More particularly in the oligomer according to the present invention, said precursor oligomer P comprises, in its structure, hydrophilic chain segments which can be water-soluble (water-soluble) or water-dispersible (dispersible in water without addition of surfactant), in particular selected from polyethers, or from polyesters, in particular polyesters based on oligoether polyols or ethoxylated polyols, or from polyurethanes based on oligoether polyols or ethoxylated polyols, in particular from polyurethanes based on oligoether polyols, in particular said segments having a number average molecular weight Mn of less than 2000, preferably less than 1000. Mn is in particular calculated from the OH, IOH, polyol or monool number expressed in mg KOH / g and its functionality in hydroxy. Mn is calculated from:
Mw = 56000 / 10OH.
The preferred hydrophilic structure for said precursor oligomer P are polyethers or oligoethers based on Mn polyoxyethylene as indicated above.
According to a more particular first option of said oligomer of the invention, depending on the selected carboxylic acid compound C), said carboxylic acid compound C) is, according to C11), an ethylenically unsaturated monoacid selected from: acrylic or methacrylic acid, crotonic acid (acid trans-2-butenoic) or β-carboxyethyl acrylate (β-CEA) or mixtures thereof, preferably acrylic or methacrylic acid or β-CEA or mixtures thereof and more preferably acrylic or methacrylic acid or mixtures thereof.
According to another more particular option, said carboxylic acid compound C) is, according to C22), a saturated dicarboxylic acid selected from: succinic acid, malonic acid, malic acid, glutaric acid (in Cs: carrier of 5 carbon atoms) adipic acid ( in Οβ), pimelic acid (C7), or diester-acids of the aforementioned diacids with a C2-C4 alkane diol or with a di-, tri- or tetraethylene glycol, or diacids among dimer and / or trimer d fatty acids, especially dimers and / or trimers of hydrogenated fatty acids (C36 dimers and C54 trimers) or mixtures thereof in particular with two or three and preferably among succinic acid, malonic acid, malic acid, acid glutaric acid (C5) or diacids among dimers and / or trimers of fatty acids, especially dimers and / or trimers of hydrogenated fatty acids or mixtures thereof.
According to a third more particular option, said carboxylic acid compound C) is according to C21) an unsaturated dicarboxylic acid and selected from: itaconic acid, maleic acid, fumaric acid, tetrahydrophthalic acid (cyclohexene dioic acid), or acid diesters of the aforementioned diacids with a C2 to C4 alkane diol or with a di-, tri- or tetra-ethylene glycol, or dimers and / or trimers of non-hydrogenated fatty acids (C36 dimers and C54 trimers) or mixtures thereof, preferably from 1 to itaconic acid, maleic acid, fumaric acid and mixtures thereof.
The structure of said oligomer of the invention and in particular the ethylenic unsaturation and its position will depend on the presence or absence of such unsaturation in said precursor oligomer P and as a function of the presence or absence of such ethylenic unsaturation in said carboxylic acid compound C) depending on whether it is saturated or unsaturated.
Said P-precursor oligomer, or it carries no aminoacrylate-acrylate end group (no acrylate), or it carries at least one aminoacrylate-acrylate end group (an acrylate) and that: a) in the case where said precursor oligomer P carries a aminoacrylate-terminal acrylate group: a1) said carboxylic acid compound C) is an ethylenically unsaturated monoacid according to C11) or a2) said carboxylic acid compound C) is an unsaturated diacid according to C21) or a saturated diacid according to C22), preferably saturated according to C22 b) in the case where said precursor oligomer P bears no aminoacrylate-terminal acrylate group, in this case: b1) said carboxylic acid compound C) is an unsaturated monoacid according to C11) and two molecules of said monoacid according to C11) are attached to said P, precursor oligomer by two ionic bonds, or b2) said carboxylic acid compound C) is an unsaturated diacid according to C21) or saturated according to C22), preferably its measured according to C22) and in the presence of an unsaturated monoacid according to C11), or b3) said carboxylic acid compound C) is an unsaturated diacid according to C21)
The functionality of the oligomer of the invention in ethylenic unsaturations will also depend on the presence or absence of ethylenic unsaturation in said precursor oligomer P and said carboxylic acid C). More particularly, the oligomer according to the invention may have a functionality of ethylenic unsaturation as follows: a ') f = 1 with said carboxylic acid compound C) being, according to C11), a salifying unsaturated monoacid (in the form of the carboxylate salt of ammonium) only one of said tertiary amine functional groups may be an aminoacrylate formed in said precursor oligomer P or optionally tertiary amine functions carried by said amine compound A), said precursor oligomer P bearing no aminoacrylate-terminal acrylate group (per molecule ), or b ') f = 2 with: - said carboxylic acid compound C) being, according to C11), an unsaturated monoacid salifying two of said tertiary amine functional groups which may be aminoacrylates formed in said precursor oligomer P and / or optionally tertiary amine functions carried by said amine compound A), said precursor oligomer P carrying no aminoacrylate group terminal acrylate (per molecule), or - said carboxylic acid compound C) being, according to C21), a saturated diacid salifying one of said tertiary amine functional groups which may be aminoacrylates formed in said precursor oligomer P or, optionally, tertiary amine functions carried by said compound amine A), and with two ammonium carboxylate bonds linking said diacid according to C21) to two molecules of said precursor oligomer P, said precursor oligomer P carrying only one aminoacrylate-terminal acrylate group (per molecule), or - said carboxylic acid compound C) being, according to C11), an unsaturated monoacid salifying one of said tertiary amine functional groups which may be aminoacrylates formed in said precursor oligomer P or, optionally, tertiary amine functional groups carried by said starting amine compound A) and said precursor oligomer P being a carrier of a single aminoacylate-terminal acrylate group, c ') f = 3 with c: - said carboxylic acid compound C) being according to C11) an unsaturated monoacid salifying three of said tertiary amine functional groups which may be aminoacrylates formed in said P-precursor oligomer and / or optionally said tertiary amine functional groups carried by said amine compound A) of departure and with said precursor oligomer P carrying no aminoacrylate-terminal acrylate group, or - said carboxylic acid compound C) being according to C11) an unsaturated monoacid salifying two functions of said tertiary amine functional groups which may be aminoacrylates formed in said P-precursor oligomer or and optionally tertiary amine functions carried by said amine compound A) as ammonium carboxylate, with said precursor oligomer P carrying a single aminoacrylate-terminal acrylate group, or - said acidic compound C) being in accordance with C22) an unsaturated diacid salifying one of said tertiary amine functions which can be e aminoacrylates formed in said precursor oligomer P or optional tertiary amine functions carried by said amine compound A) in each of two precursor P oligomer molecules, said precursor oligomer P carrying a single aminoacrylate group; terminal acrylate per molecule, or - said carboxylic acid compound C) being according to C11) an unsaturated monoacid salifying one of said tertiary amine functional groups which may be aminoacrylates formed in said precursor oligomer P or optionally tertiary amine functional groups carried by said amine compound A) starting material, with said precursor oligomer P carrying two aminoacrylate-terminal acrylate groups per molecule, or - said carboxylic acid compound C) being a mixture of an unsaturated diacid according to C22) and an unsaturated monoacid according to C11), with said diacid according to C22) associating by salification two molecules of said P aya precursor oligomer each of said molecules, one of said tertiary amine functional groups possibly being aminoacrylates formed in said precursor oligomer P or optionally tertiary amine functions carried by said amine compound A), salified by said diacid according to C22) and a second of said amine functions tertiary salts salified with said monoacid according to C11), said (final) oligomer carrying four ammonium carboxylate ionic bonds, or - said carboxylic acid compound C) being a saturated diacid according to C21) associating by salification two precursor oligomers P, one of which one aminoacrylate-terminal acrylate function (per molecule) and the other two terminal aminoacrylate-acrylate functions (per molecule) of) f = 4, with: - said carboxylic acid compound C) being an unsaturated monoacid according to C11) salifying four of said tertiary amine functions which may be aminoacrylates formed in said P or / and precursor oligomer and optionally tertiary amine functions carried by said amine compound A), said oligomer P carrying no aminoacrylate-terminal acrylate group per molecule or said carboxylic acid compound C) being a saturated diacid according to C21) and combining two molecules of said oligomer precursor P by salification of one of said tertiary amine functional groups which may be aminoacrylates formed in said precursor oligomer P or optionally tertiary amine functions carried by said amine compound A) in each of two molecules of said precursor oligomer P and with said precursor oligomer P carrying 2 aminoacrylate-terminal acrylate groups per molecule or - said carboxylic acid compound C) being a diacid saturated according to C21) and combining two molecules of said precursor oligomer P by salification of one of said tertiary amine functional groups which may be aminoacrylates formed in said ol P precursor oligomer or optionally tertiary amine functions carried by said amine compound A) in each of two molecules of said precursor oligomer P and with a first precursor oligomer P carrying 2 aminoacrylate-terminal acrylate groups per molecule and one the second being carrying a single aminoacrylate-acrylate group, or - said carboxylic acid compound C) being an unsaturated monoacid according to C11) salifying three of said tertiary amine functional groups which may be aminoacrylates formed in said precursor oligomer P and / or optional functions tertiary amines carried by said amine compound A), with said precursor oligomer P carrying only one aminoacrylate-acrylate group per molecule), or - said carboxylic acid compound C) being an unsaturated monoacid according to C11) salifying two of said Tertiary amine functions that can be formed aminoacrylates in said precursor oligomer P and / or optionally tertiary amine functional groups carried by said amine compound A), with said precursor oligomer P carrying two aminoacrylate-terminal acrylate groups per molecule, or - said carboxylic acid compound C) is a monoacid unsaturated according to C11) salifying one of said tertiary amine functional groups that may be aminoacrylates formed in said precursor oligomer P or optionally tertiary amine functions carried by said amine compound A) starting with said precursor oligomer P carrying three aminoacrylate-terminal acrylate groups by molecule, with, in the case where a diacid according to C21) or C22) is used to associate by salification two molecules of said precursor oligomer P, said molecules of said precursor oligomer P may be identical or different structure.
According to a particular option, the components of said precursor oligomer P, that is to say the amine compound A) and / or the hydrophilic acrylate compound B) can be respective mixtures of compounds A) or / and B). Similarly, said precursor oligomer P may be a mixture of precursor oligomers P different in structure and in functionality and / or said carboxylic acid compound C) may be a mixture of different carboxylic acids C) (of different structure).
In particular, said amine compound A) may be a mixture of amine compounds A) as defined above and / or said acrylate compound B) may be a mixture of compounds B) as defined above and / or said compound acid C) may be a mixture of compounds C) as defined above. Also, said acid compound C) may be a mixture, in particular a mixture of ethylenically unsaturated monoacids according to C11) or a mixture of ethylenically unsaturated diacids according to C21) or a mixture of saturated diacids according to C22) or a mixture of said acids according to C11) and according to C21) and possibly according to C22.
More particularly, said amine compound A) may be a mixture of amine compounds A) as defined above and in particular a mixture of amine compounds according to A1) or according to A2) or a mixture of amine compounds according to A1) and according to A2), with said compounds according to A1) or according to A2) being as defined according to the invention above. Similarly, the acrylate compound B) may be a mixture of at least one monofunctional acrylate compound, which may in particular be a mixture of monofunctional acrylate compounds and at least one multifunctional acrylate compound, which may in particular be a mixture of multifunctional acrylate compounds of different chemical nature and identical or different functionality or of identical nature and different functionality.
In the case of mixtures, the functionality referred to corresponds to the average number function fmoy which is calculated according to the following formula (4): fmoy = Ii (ni * fi) (4) with Σϊ (n,) = 1 and ni being the fraction in number of molecules i of functionality fj.
Said P-precursor oligomer can be defined in particular according to the following general formula (I): [[R 1 (R 2) N] x- [R '3 -N (R' 4)] n -R 3 -N (R 4) - CH2CH2-CO2] rR5- (CO2-CH = CH2) (ny) (I) with:
R 1, R 2 being C 1 -C 4 alkyl of a tertiary amine other than an aminoacrylate wherein R 1 = R 2 and R 2 N =, being a group including an aminoacrylate bond R 6 -O 2 CCH 2 CH 2 N- and in this case with R 1 or R 2, which are identical or different, and corresponding to R6-O2CCH2CH2-, with R6 being the residue of a monoacrylate compound, in particular a polyether diol monoacrylate or a polyether monoalcohol monoacrylate. R3: residue of said amine compound A), if carrying a primary amine function and optionally a tertiary amine function, with z = 0 and signifying the absence of secondary amine function in the presence of the primary amine function, R ' 3: is for z = 0 and x = 1, a single bond between R3 and the tertiary amine group "R- (R2) N-", said amine compound A carrying a primary amine function and a tertiary or R'3: is C2 to C6 alkylene for z = 1 and x = 1 with said amine compound having a primary amine function a secondary amine function and a tertiary amine function, R4: for z = 0, is C1-C4 alkyl when said amine compound A) carries a secondary amine function and optionally a tertiary amine function, otherwise when said amine compound A) carries a primary amine function, in this case R4: - [CH2CH2-CO2] y -R5- (CO2-CH = CH2) (ny) or R4: at least in part is -CH2CH2-CC>2-R'5 when there is presence of monofunctional acrylate radical R's in addition to the ac multifunctional rylate, with R's being able to comprise a free hydroxyl group, R'4: - [CH2CH2-CO2] y -R5- (CO2-CH = CH2) (ny) when z = 1 signifying the simultaneous presence of a primary amine function with a secondary
Rs: residue of said multifunctional acrylate compound B selected in particular from the residues of polyethers, polyesters or from polyurethane residues based on polyesters and polyether polyols, x = 1 if amine A carries a tertiary amine function and 0s the absence of such a tertiary amine function z = 1 if presence of secondary amine function at the same time as the primary amine function in the amine compound A) and z = 0 if no secondary amine function n is present: initial functionality of said acrylate B ranging from 1 to 6, preferably from 1 to 4 y: number of aminoacrylate groups created by addition reactions of an NH of said amine compound A on an acrylate group of said acrylate B, with 'y' ranging from 1 to 6 preferably from 1 to 4 and ny: from 0 to 3 and preferably from 0 to 2, represents the number of residual acrylate groups in said P oligomer.
The choice of amine A) can determine the choice of acrylate B. According to a first particular option, said amine compound A) is an amine compound according to A1) as defined according to the invention above and said acrylate compound B) comprises at least one multifunctional acrylate compound according to B1) and at least one monofunctional acrylate compound according to B2) and preferably said multifunctional acrylate compound according to B1) is a partial or complete multifunctional ester of at least one polyether polyol or at least one at least one polyol derived from said polyether with acrylic acid and said monofunctional acrylate compound according to B2) is a monoester of acrylic acid with at least one polyether diol or monool or at least one diol or monool derived from said polyether, more particularly said polyethers being polyoxyethylenes and having a number-average molecular weight Mn of less than 2000 and preferably less than 1000. The Mn is calculated as explained below. from the OH number and the functionality of said polyether polyols or monools.
According to a second particular option, said amine compound A) is an amine compound according to A2) as defined according to the above claim and preferably said acrylate compound B) is a multifunctional acrylate compound according to B1) selected from partial or complete esters by the acrylic acid of a polyether polyol or a polyol derived from said polyether, or from urethanes acrylates from a polyether polyol or from epoxy acrylates from a glycidyl polyether, more particularly said polyethers being polyoxyethylenes and having a number average molecular weight Mn less than 2000 and preferably less than 1000. The Mn is calculated as explained above from the OH number and the functionality of said polyether polyols or monools.
More particularly, the functionality of said polyols as base of said multifunctional acrylates according to B1) can vary from 2 to 6 and preferably from 2 to 4. The number of ethoxy units per hydroxy function of said polyol for the ethoxylated polyols can vary from 2 to 20 and preferably from 3 to 20 and more preferably from 5 to 20.
The acrylate urethanes according to B1) from polyether polyols can be obtained by reacting a polyether polyol, in particular a polyoxyethylene polyol with a monoisocyanate precondensate obtained by reacting a hydroxyalkyl acrylate such as hydroxy ethyl acrylate (HEA ) with a diisocyanate.
The epoxy acrylates according to B1, from multifunctional glycidyl polyethers (glycidyl ethers of a polyether polyol), in particular polyoxyethylene polyol glycidyl ethers, can be obtained by reaction of said glycidyl ethers of polyether polyols (epoxidized polyethers) with acrylic acid.
As suitable examples of ethoxylated polyols for multifunctional acrylate esters according to B1), mention may be made of ethoxylated trimethylol propane (3 OH), ethoxylated pentaerythritol (4 OH), ethoxylated di (ethoxylated) trimethylol propane (4 OH) and ethoxylated dipentaerythritol (6 OH). ), ethoxylated sorbitol (3 OH), ethoxylated oligosters polyols, polyoxyethylene polyols, ethoxylated bisphenol A (2 OH), ethoxylated isosorbide (20H), ethoxylated tricyclodecanedimethanol (2 OH, ethoxylated neopenthyl glycol (2 OH), ethoxylated glycerol (3 OH)). These ethoxylated polyols are perfectly suitable for obtaining, by complete or partial acrylation (as the case may be, if OH functionality of at least 3), the multifunctional acrylate esters according to B 1, More particularly, the multifunctional acrylate according to B 1 can be a polyethylene glycol diacrylate. Mn variable from 150 to 600, bisphenol A ethoxylated diacrylate with an ethoxy number ranging from 4 to 15 such as SR 349, SR 601, SR 602 from Sartomer or trimethylolpropane ethoxylated triacrylate with a number of ethoxy units ranging from 3 to 20 such as SR 454, SR 499, SR 502, SR 9035 or SR 415 from Sartomer or glycerol ethoxylated triacrylate with 3 to 15 ethoxy such as SR 9046 from Sartomer, or ethoxylated pentaerythritol tetraacrylate with 3 to 15 ethoxy such as SR 494 from Sartomer.
As the amine compound A), the following categories can be distinguished for the amine compound according to A1), as defined above: A11) Primary monoamines, with as examples of primary monoamines which may be suitable, the following amines: N-alkylamines such as amylamine, 2-aminopentane, 3-aminopentane, 1,2-dimethylpropylamine, hexylamine, 1,3-dimethylbutylamine, n-heptylamine, n-octylamine, 2-aminooctane, 3,3,5-trimethylcyclohexylamine, ethylamine, isopropylamine, sec-butylamine, N-alkylamines carrying hydroxyl groups such as Alaninol, N-alkoxyamines such as 3-ethoxypropylamine, 3- (2-methoxyethoxy) propylamine, 3-butoxypropylamine, 3- (2-ethylhexyloxy) propylamine, 3-lsopropoxypropylamine (IPOPA), 3-methoxypropylamine (ΜΟΡΑ), polyether amines such as Jeffamine® M600, M1000 marketed by Hunstman, amines carrying specific functions such as 1- (2-aminoethyl) -2-imidazolidinone also called UDETA (urea diea ethylene triamine), amide-amino compounds (from a diacid and an excess primary diamine) or amino ester-amide compounds (from an acid ester with a primary diamine of excess), A12) primary-secondary diamines with N-alkylaminoalkylamines, such as N-methyl-1,3-diaminopropane, N-propyl-1,3-propane diamine, N-isopropyl-1,3- propane diamine, N-cyclohexyl-1,3-propanediamine, triacetone diamine, 1,2-diaminocyclohexane (1,2-DACH), bis (4-aminocyclohexyl) methane (PACM) or the N-alkylaminoalkylamines carrying hydroxyl groups, in hydroxyalkylaminoalkylamines, such as 2- (3-aminopropylamino) ethanol, A13) primary-primary diamines, with suitable examples that may be mentioned: alkylenediamines or cycloalkylenediamines such as 1,3-bis (aminomethyl) cyclohexane ( 1,3-BAC), isophorone diamine (IPDA) or polyether diamines with 2 to 20 ethoxy and / or propoxy ether units, such as Jeffamine® sold by Hunstman under the trade names D230, D400, ED600, ED900, EDR148, EDR 176, EDR 104, THF 100, THF 140, THF 230, RFD 270 or fatty amines derived from C36 fatty acid dimers as marketed by Croda under the trade name Priamines®,
A14) primary-tertiary diamines with suitable examples that may be mentioned: N, N dialkylaminoalkylamines such as diethylaminopropylamine (DEAPA), dimethylaminopropylamine (DMAPA), 3- (dibutylamino) propylamine, N, N-dimethylethylenediamine, or 1- (3-aminopropyl) -2-pyrrolidine, 3-morpholinopropylamine, 1- (3-aminopropyl) piperidine, 1- (3-aminopropyl) -2-pipecoline, the N, N-dialkylaminoalkylamines carrying hydroxyl groups, in particular dihydroxyalkyl aminoalkyl amines such as N- (aminopropyl) diethanolamine (APDEA), A15) The primary-secondary-tertiary triamines with suitable examples that may be mentioned that include: Ν, Ν-dimethyldipropylene triamine (DMAPAPA), N-aminoethylpiperazine, 3- (2-aminoethyl) aminopropylamine, bis (3-aminopropyl) amine, methyl bis (3-aminopropyl) amine, N- (3-aminopropyl) -1,4-diaminobutane.
As the amine compound A), the following classes may be distinguished for the amine compound according to A2, as defined above: A21) the secondary monoamines with, as suitable examples, N, N dialkylamines, such as di-sec-butylamine, diamylamine, isopropylbenzylamine, dihexylamine, diethylamine, diisopropylamine, N-isopropylmethylamine, N-butylmethylamine, N-sec-butylmethylamine, N-isobutylmethylamine, N-tert-butylmethylamine, N-methylpentylamine, N-hexylmethylamine, N- methylcyclohexylamine, N-heptylmethylamine, N-octylmethylamine, N-ethylmethylamine, N-ethylpropylamine, N-ethylisopropylamine, N-butylethylamine, N-sec-butylethylamine, N-ethylcyclohexylamine, N-ethylbenzylamine, the N, N dialkylamines carrying hydroxyl groups such as 2- (ethylamino) ethanol, 2- (isopropylamino) ethanol, 2-butylaminoethanol, 2-benzylaminoethanol, 2-octylaminoethanol, 2-sec-butylaminoethanol, A22) Secondary-secondary diamines with Examples which are suitable are: N, N 'dialkyl alkyl diamines such as N, N' dimethyl ethylene diamine or N, N 'dialkyl cycloalkylene diamines or bis (N, N' dialkyl cycloalkylene) alkylene such as cycloaliphatic secondary diamines under the trade name JEFFLINK® 136 and 754 sold by Hunstman, A23) Secondary-tertiary diamines with N, N, N'-trimethyl-1,3-propanediamine or epoxy-amine amino adducts as suitable examples.
Preferred amine compounds A), amine compounds according to A1) and more particularly amine compounds: diamines according to A12) primary-secondary, according to A13) primary-primary, according to A14) primary-tertiary or triamines according to A15) primary -secondary-tertiary and even more particularly diamines according to A13) or according to A14) and triamines according to A15). According to a more particular option, said amine compound A) is according to A1) and selected according to A14).
With regard to the functionality of said oligomer, it preferably carries, as ethylenic unsaturation, acrylate groups with a functionality in acrylate groups, including ammonium acrylate if the acrylic acid is used as carboxylic acid compound C), ranging from 1 to 6, preferably from 1 to 4, more preferably from 1 to 3. More particularly, said oligomer according to the invention carries at least 2 acrylate groups per oligomer and is therefore more particularly crosslinkable, which means alone without the need for a crosslinking agent.
With regard to the level of tertiary amine sites, including aminoacrylates formed by adding said amine compound A) to said acrylate B), which are converted to the ammonium carboxylate salt, it can be represented by the tertiary amine function rate as well as salified. Preferably, the oligomer according to the invention has a level of tertiary amine functions salified ranging from 0.1 to 25, preferably from 0.5 to 15 mEq per g of said oligomer. Preferably, said oligomer has a number average molecular weight Mn calculated by the material balance, is less than 5000, preferably less than 3000. The invention also covers the precursor oligomer P, precursor of the oligomer as defined according to US Pat. invention herein, in particular comprising or being an oligomer according to formula (I) as defined above.
A second subject of the invention relates to an oligomer solution in a reactive diluent, which comprises the oligomer as defined above according to the invention and at least one reactive diluent D) selected from mono (meth) acrylates and / or the multifunctional (meth) acrylates, preferably with D) being a (meth) acrylate of a polyether monool or polyol or of a polyether monool or polyol derivative, with a number-average molecular weight Mn less than or equal to 600. This Mn mass is calculated from Ioh and the functionality of said monool or polyol and its functionality as discussed above.
Another subject of the present invention relates to a process for preparing said oligomer as defined above according to the invention, which comprises the following successive stages: i) Preparation of said precursor oligomer P by the addition of at least one amine compound A), according to A1) and / or according to A2) as defined above for A) according to the invention, on B) an acrylate compound from: - B1) at least one multifunctional acrylate having a functionality, in particular an average functionality in number if mixture, ranging from 2 to 6 and preferably from 2 to 4, more preferably from 2 to 3, more preferably from 2 when said amine compound A) is a compound according to A2) as defined above for the amine compound A) or - a mixture of at least one multifunctional acrylate according to B1) as defined above and at least one monofunctional acrylate according to B2), when said amine compound A) is an amine compound according to A1, such that defined above for the co amine compound A), this to block by the aminoacrylate formed one of two -NH groups of said primary amine function of said amine compound according to A1), with the following molar ratios between groups:
(acrylate) / (-NH)> 1 so that at least one residual acrylate group is carried by the addition product i) corresponding to said precursor oligomer P and in the case where said amine compound A) is according to A1, said acrylate B) is a multifunctional acrylate mixture according to B1) and monofunctional acrylate according to B2) with a molar ratio B2 / A1 = 1/1 ii) Salification of said precursor oligomer P which is the product of the addition step i), in the form of ammonium carboxylate salt with said carboxylic acid compound C), as defined above according to the invention, preferably with a molar ratio of carboxy groups to tertiary amine functions (= N-) y including tertiary amines among aminoacrylate groups (carboxy) / (tertiary amine) ranging from 0.10 to 1.00, preferably from 0.5 to 1.00 and more preferably from 0.5 to 0.99.
Also part of the invention is a polymerizable oligomer, in particular crosslinkable, as obtained by the process as defined above according to the invention.
Another subject of the invention relates to a polymerizable composition, in particular a crosslinkable composition, which comprises as binder at least one oligomer as defined above according to the invention or obtained by a process as defined above according to the invention or a solution as defined above according to the present invention.
More particularly, said composition is polymerizable, in particular crosslinkable, by: - radiation pathway, in particular UV, LED, laser, electron beam preferably UV, - thermal pathway or peroxide or hydroperoxide in the presence of a accelerator, dual channel combining at least two of the aforementioned routes, and preferably by radiation, more preferably by UV.
Even more particularly, it is a polymerizable composition, in particular a crosslinkable composition, for a material with a temporary function, preferably among coatings, in particular ink, varnish, adhesive, or among hydrogel or support material for a 3D printing object. per layer, more preferably coating, or support material for 3D printing object layer by layer, and even more preferably for 3D printing object support material layer by layer.
Another subject of the present invention relates to the use of an oligomer as defined above according to the invention or of an oligomer solution as defined according to the invention or the use of the oligomer obtained by a process as defined according to the invention, as a polymerizable binder and in particular a crosslinkable binder, optionally water-soluble, in polymerizable and in particular crosslinkable compositions, preferably under radiation. Said use is particularly applicable to a material with a temporary function, removable by washing with water alone or with saline water or with another aqueous solution, preferably having a pH> 7 more preferably> 8, in particular with materials with a temporary function among coatings, hydrogels or a support material for 3D printing object layer by layer, more particularly coatings or support material for 3D printing object layer by layer.
Even more particularly, said use is specifically applicable to the printing of 3D objects by polymerization, in particular crosslinking, under layer-by-layer radiation, of a composition comprising said oligomer or said oligomer solution as a material with a temporary support function. or consolidating or molding said final 3D object, obtained after removal of said temporary function material by washing with water or with a saline solution or with another aqueous solution.
Another possible use relates to hydrogels obtained from the crosslinking of a crosslinkable composition comprising said oligomer or said oligomer solution followed by swelling with water or a suitable aqueous solution. Such use may in particular relate to the transport of pharmaceutical or phytosanitary active ingredients or for the treatment of wood by using said hydrogels as a carrier or vector of said pharmaceutical, phytosanitary or wood treatment active ingredient.
Finally, it is also part of the present invention, a polymeric material, in particular crosslinked, which results from the use as polymerizable binder, in particular crosslinkable of at least one oligomer according to the invention as defined above or of an oligomer obtained by the process of the invention as defined above or an oligomer solution according to the invention as defined above or the polymerization, in particular of the crosslinking, of a polymerizable composition , in particular crosslinkable according to the invention, as defined above.
More particularly, said material is a material with a temporary function, removable by water, a saline solution or another aqueous solution adapted to this elimination, for example by adjusting the pH to> 7, in particular pH to> 8, preferably among the coatings, hydrogels or a material for supporting or consolidating or molding a printed object in 3D layer by layer under radiation and more preferably a temporary material for supporting or consolidating or molding a printed object in 3D layer by layer under radiation.
The following examples are presented to illustrate the invention and its performance and in no way limit its scope.
EXAMPLES 1) Preparation and formulation of oligomers according to the invention
Example 1
In a 1L reactor, 108.54 g of dimethylaminopropylamine (DMAPA from Huntstman, Mw of 102.18 g / mol) and 0.14 g of 2,6-di-tert-butyl-4-methylphenol (BHT) are introduced. . Under agitation and bubbling with air, 356.93 g of polyethylene glycol monoacrylate (Bisomer PEA6 from Geo Specialty Chemicals, Mw of 336 g / mol) are added at ambient temperature over one hour at a constant flow rate. An exotherm of about 20 ° C is observed. At the end of the addition, the temperature of the mixture is raised to 60 ° C. After four hours at 60 ° C., 464.22 g of butane diol diglycidyl ether diacrylate (BDDGEDA, CN132 from Sartomer, Mw of 256.8 g / mol) are added to the mixture in thirty minutes at a constant rate. At the end of the addition, the temperature of the mixture is maintained at 60 ° C for three hours, then 70.17 g of glutaric acid (Aldrich, 132.11 g / mol) is added to the mixture. At the end of the addition, an additional reaction time of one hour at 60 ° C is observed before recovering the final product.
Example 2
In a 1L reactor, 125.68 g of dimethylaminopropylamine (DMAPA from Huntstman, Mw of 102.18 g / mol) and 0.93 g of 2,6-di-tert-butyl-4-methylphenol (BHT) are introduced. . Under stirring and bubbling with air, 413.27 g of polyethylene glycol monoacrylate (Bisomer PEA6 from Geo Specialty Chemicals, Mw of 336 g / mol) are added at ambient temperature over one hour at a constant flow rate. An exotherm of about 20 ° C is observed. At the end of the addition, the temperature of the mixture is raised to 60 ° C. After four hours at 60 ° C., 371.45 g of polyethylene glycol diacrylate (SR259 from Sartomer, Mw of 302 g / mol) are added to the mixture in thirty minutes at a constant rate. At the end of the addition, the temperature of the mixture is maintained at 60 ° C for three hours and then 88.68 g of acrylic acid (Aldrich, 132.11 g / mol) is added. At the end of the addition, an additional reaction time of one hour at 60 ° C is observed before recovering the final product.
Example 3
In a 1L reactor, 131.16 g of dimethylaminopropylamine (DMAPA from Huntstman, Mw of 102.18 g / mol) and 1.01 g of 2,6-di-tert-butyl-4-methylphenol (BHT) are introduced. . With stirring and bubbling with air, 775.29 g of polyethylene glycol diacrylate (SR259 from Sartomer, Mw of 302 g / mol) are added at ambient temperature over one hour at a constant flow rate. An exotherm of about 20 ° C is observed. At the end of the addition, the temperature of the mixture is raised to 60 ° C. After four hours at 60 ° C, 92.55 g of acrylic acid (Arkema, Mw 72.1 g / mol) are added over thirty minutes at a constant rate. At the end of the addition, a reaction time of one hour at 60 ° C is observed before recovering the final product.
Example 4
In a 1L reactor, 80.89 g of dimethylaminopropylamine (DMAPA from Huntstman, Mw of 102.18 g / mol) and 0.81 g of 2,6-di-tert-butyl-4-methylphenol (BHT) are introduced. ). Under agitation and bubbling with air, 554.13 g of polyethylene glycol monoacrylate (Bisomer PEA6 from Geo Specialty Chemicals, Mw of 336 g / mol) are added at ambient temperature over one hour at a constant flow rate. An exotherm of about 20 ° C is observed. At the end of the addition, the temperature of the mixture is raised to 60 ° C. After four hours at 60 ° C, 114.15 g of acrylic acid (Aldrich, 132.11 g / mol) are added to the mixture in thirty minutes at a constant rate. At the end of the addition, a reaction time of one hour at 60 ° C. is observed. 250 g of polyethylene glycol diacrylate (SR 344 from Sartomer) as dilution monomer or reactive diluent are then added. An additional homogenization time of 30 minutes at 60 ° C is observed before recovering the final product. 2) Comparative examples
As a reference for comparison, crosslinkable compositions representative of the state of the art comprising, in addition to reactive components without aminoacrylates, non-reactive water-soluble components such as polyethylene glycol 600 (PEG 600) are used.
Example 5
In a 1L reactor, 626 g of polyethylene glycol of mass 600, 368 g of polyethylene glycol of mass 600 diacrylate (SR 610 of Sartomer) and 6 g of propoxylated glycerol triacrylate (SR 9020 from Sartomer) are introduced. With stirring and bubbling with air, the mixture is heated to 60 ° C. A mixing time of thirty minutes at 60 ° C is observed. Example 6
In a 1L reactor, 337 g of polyethylene glycol of mass 600, 342 g of polyethylene glycol of mass 600 diacrylate (SR 610 from Sartomer), 315 g of polyethylene glycol monoacrylate (Bisomer PEA6 from Geo Specialty Chemicals, Mw of 336) are introduced. g / mol) and 6 g of propoxylated glycerol triacrylate. With stirring and bubbling with air, the mixture is heated to 60 ° C. A mixing time of thirty minutes at 60 ° C is observed. 3) Characteristics of the compositions before crosslinking
Table 1
4) Evaluation of the properties of the crosslinked compositions and the hydrofragmentation performances in an aqueous solution
For the compression and hydro-fragmentation tests, the products as described according to the invention (Example 3 and 4) and the comparative compositions (Examples 5 and 6) are formulated with an overall photoinitiator content of 5% by weight. composed of 4% Irgacur® 1173 (BASF) and 1% by weight of Lucirin® TPO-L (BASF) for 95% by weight of the composition tested in Table 1. The crosslinking is carried out under a 120 Watt / cm UV lamp. Compression test (according to standard NF EN ISO 604)
Type of test pieces; Cylindrical (diameter: 13.3 mm, height 26.5 mm) obtained by crosslinking under a UV lamp 120 Watt / cm of a composition contained in a cylindrical mold in sacrificial glass having the dimensions (diameter) corresponding to those of the test tube (length adjusted by cutting the crosslinked object).
Testing machine: INSTRON 1185 ReNew, cell 10kN
Test speed: 1.3 mm / min.
The test pieces were tested at 23 ° C.
The results are shown in Table 2 below.
Table 2
Hydro-fragmentation test
The hydro-fragmentation test is defined as follows:
A mass-cured object in the form of a 15 g and 15 cm 3 cylinder (2 cm high, 1.5 cm radius) is immersed for two hours in a bath containing 400 ml of an aqueous solution of water. sodium hydrogencarbonate (pH> 7) at 60 ° C., with magnetic stirring (magnetic bar). After two hours of treatment, the mixture is filtered and the residual solids dried.
Two criteria are then measured and evaluated: 1) The weight of the cylinder before the test, then after filtration and drying, indicates the part of the object passed in solution, "water-soluble" or "hydrodispersible" 2) The appearance of the cylinder after the test: a mark of 0 to 5 is awarded; it indicates the degree of "hydro-fragmentability" of the material. at. 0: the original cylinder remained intact b. 5: the cylinder is completely fragmented, the solid residuals being in the form of homogeneous powder after filtration and drying
The cylindrical objects prepared for the test are obtained from a Teflon mold. 20 passes under a 120 Watt / cm UV lamp are required to obtain the crosslinked object. The results are shown in Table 3 below.
Table 3
*: homogeneously sized particles with a maximum size of less than 7 mm **: particles of uniform size with a maximum size of less than 5 mm ***: particles of very variable size (very heterogeneous) with a maximum maximum size of greater than 20 mm

权利要求:
Claims (28)
[1" id="c-fr-0001]
Polymerizable oligomer, in particular crosslinkable, characterized in that it carries at least one ethylenic unsaturation and at least one ionic bond of ammonium carboxylate and in that it comprises in its structure or in its composition: - P) at least one precursor oligomer carrying at least one tertiary amine function in the form of an aminoacrylate group, preferably at least two tertiary amine functions in the form of aminoacrylate groups, resulting from the addition of at least one an amine compound according to A1) carrying at least one primary amine (-NH2) or / and secondary (-NH) function and optionally at least one tertiary amine and / or A2 function) carrying at least one secondary amine function (-NH) and optionally at least one tertiary amine function on B) at least one hydrophilic acrylate compound and thus forming said at least one aminoacrylate group, and - C) at least one carboxylic acid compound e attached to said precursor oligomer P by at least one ionic linkage of ammonium carboxylate with at least one of said aminoacrylate groups and optionally at least one of said tertiary amine functions of said amine compound A) preferably said oligomer carrying at least two ionic carboxylate ammonium bonds as defined above.
[2" id="c-fr-0002]
2. Oligomer according to claim 1, characterized in that said amine compound A) is selected from: - A1) an amine compound, carrying at least one, in particular a primary amine function and optionally at least one , in particular a tertiary amine function and / or at least one, in particular a secondary amine function, and / or - A2) an amine compound carrying at least one, in particular a secondary amine function and optionally at least one, in particular a tertiary amine function, and in that said acrylate compound B) is at least one multifunctional acrylate compound according to B1) and / or monofunctional according to B2), and in particular for A) being or comprising an amine compound according to A1), said acrylate compound B) is a mixture of at least one multifunctional acrylate according to B1) and at least one monofunctional acrylate according to B2).
[3" id="c-fr-0003]
3. Oligomer according to claim 2, characterized in that said hydrophilic acrylate compound B) is a mixture of multifunctional acrylate compound according to B1) and monofunctional acrylate compound according to B2).
[4" id="c-fr-0004]
4. Oligomer according to one of claims 1 to 3, characterized in that said aminoacrylate group may carry at least one ethylenic unsaturation, in particular acrylate, or no ethylenic unsaturation and, in the latter case, said acidic compound C) is ethylenically unsaturated.
[5" id="c-fr-0005]
5. Oligomer according to one of claims 1 to 4, characterized in that said acid compound C) is a monoacid according to C1) which is ethylenically unsaturated according to C11) and said oligomer carries at least two ionic carboxylate ammonium bonds.
[6" id="c-fr-0006]
6. Oligomer according to one of claims 1 to 5, characterized in that - when said carboxylic acid compound C) is according to C1) a monoacid, in this case: C1) is a monoacid according to C11) ethylenically unsaturated and at least one ethylenic unsaturation of said oligomer is carried by at least said monoacid according to C11) by ammonium carboxylate linkage with at least one of said tertiary amine functions from said aminoacrylate groups or optionally from the tertiary amine functions carried by said amine compound A), and optionally at at least one other ethylenic unsaturation of said oligomer is carried by at least one aminoacrylate group in the form of aminoacrylate-terminal acrylate group of said precursor oligomer P or C1) is a saturated mono (C12) acid and at least one ethylenic unsaturation of said oligomer is carried by at least one an aminoacrylate group in the form of an aminoacrylate-terminal acrylate group of said ol precursor oligomer P, preferably said monoacid according to C1) being according to C11) an unsaturated monoacid, and when said carboxylic acid compound C) is in accordance with C2) a polycarboxylic acid and preferably a diacid, in this case: C2) is a polyacid according to C21) ethylenically unsaturated, in particular ethylenically unsaturated diacid, and at least one ethylenic unsaturation said oligomer is carried by at least said polyacid according to C21) and optionally in addition, at least one ethylenic unsaturation is carried by at least one aminoacrylate group in the form of aminoacrylate-terminal acrylate groups of said precursor oligomer P or C2) is a polyacid according to C22) saturated, in particular saturated diacid, and said precursor oligomer P carries at least one aminoacrylate-terminal acrylate group and said oligomer which results carries at least two ethylenic unsaturations acrylates.
[7" id="c-fr-0007]
7. Oligomer according to claim 6, characterized in that said carboxylic acid compound C) is an unsaturated diacid according to C21) or saturated according to C22) associating with two carboxylate ionic bonds, two molecules of said precursor oligomer P, by salification in the form of salt. ammonium carboxylate of one of said tertiary amine functional groups from said aminoacrylate groups formed or optionally from said tertiary amine functions of said amine compound A), on each of said molecules of said P oligomer, or in that said carboxylic acid compound C) is a monoacid according to C1), ethylenically unsaturated according to C11) having a polymerizable ethylenic unsaturation and in that said monoacid according to C11) salifies at least two of said tertiary amine functions in the form of ammonium carboxylate.
[8" id="c-fr-0008]
8. Oligomer according to one of claims 1 to 7, characterized in that said precursor oligomer P comprises in its structure, hydrophilic chain segments, in particular selected from polyethers, or from polyesters, in particular polyesters based on oligoether polyols or ethoxylated polyols, or from polyurethanes based on oligoether polyols or ethoxylated polyols, in particular from polyurethanes based on oligoether polyols, in particular said segments having a number average molecular weight Mn of less than 2000, preferably less than 1000.
[9" id="c-fr-0009]
9. Oligomer according to one of claims 1 to 8, characterized in that said carboxylic acid compound C) is according to C11) an ethylenically unsaturated monoacid selected from: acrylic or methacrylic acid, crotonic acid (trans-2-butenoic acid) or β-carboxyethyl acrylate (β-CEA) or mixtures thereof, preferably acrylic or methacrylic acid or β-CEA or their mixtures and more preferably acrylic or methacrylic acid or mixtures thereof.
[10" id="c-fr-0010]
10. Oligomer according to one of claims 1 to 8, characterized in that said carboxylic acid compound C) is according to C22) a saturated dicarboxylic acid and selected from: succinic acid, malonic acid, malic acid, glutaric acid (Cs: carrier of 5 carbon atoms) adipic acid (in Cq), pimelic acid (C7), or diester-acids of the aforementioned diacids with a C2-C4 alkane diol or with a di-, tri- or tetraethylene glycol, or diacids among dimers and / or trimers of fatty acids, in particular dimers and / or trimers of hydrogenated fatty acids (C36 dimers and C54 trimers) or their mixtures, in particular with two or three, and preferably from succinic acid, malonic acid, malic acid, glutaric acid (in Cs) or diacids among dimers and / or trimers of fatty acids, in particular dimer and / or trimers of hydrogenated fatty acids or mixtures thereof.
[11" id="c-fr-0011]
11. Oligomer according to one of claims 1 to 8, characterized in that said carboxylic acid compound C) is according to C21) an unsaturated dicarboxylic acid and selected from: itaconic acid, maleic acid, fumaric acid, tetrahydrophthalic acid (cyclohexene dioic acid) ), or acid diesters of the aforementioned diacids with a C 2 -C 4 alkane diol or with a di-, tri- or tetra-ethylene glycol, or dimers and / or trimers of non-hydrogenated fatty acids (C36 dimers and trimers of C54) or mixtures thereof, preferably itaconic acid, maleic acid, fumaric acid and mixtures thereof.
[12" id="c-fr-0012]
12. Oligomer according to one of claims 1 to 8, characterized in that said amine compound A) is a mixture of amine compounds A) as defined in claim 1 or 2 and / or in that said acrylate compound B) is a mixture of compounds B) as defined according to one of claims 1 to 4 and / or in that said acid compound C) is a mixture of compounds C) as defined according to one of claims 1, 4 to 7 and 9 to 11.
[13" id="c-fr-0013]
13. Oligomer according to one of claims 1 to 12, characterized in that said precursor oligomer P is defined according to the following general formula (I): [[R 1 (R 2) N] x- [R '3 -N ( R'4) z-R3-N (R4) -CH2CH2-CO2] rR5- (CO2-CH = CH2) (ny) (I) with R1, R2 being C1-C4 alkyl of a tertiary amine different from an aminoacrylate where R 1 -N = and R 2 -N =, being a group including an aminoacrylate bond R 6 -O 2 CCH 2 CH 2 N- and in this case with R 1 or R 2 which are identical or different and corresponding to R 6 -O 2 CCH 2 CH 2 -, with R 6 being the residue of a monoacrylate compound, in particular a polyether diol monoacrylate or a polyether monoalcohol monoacrylate. R3: residue of said amine compound A), if carrying a primary amine function and optionally a tertiary amine function, with z = 0 and signifying the absence of secondary amine function in the presence of the primary amine function, R ' 3: is for z = 0 and x = 1, a single bond between R3 and the tertiary amine group "Rr (R2) N-", said amine compound A carrying a primary amine function and a tertiary or R'3: is a C2 to Οβ alkylene for z = 1 and x = 1 with said amine compound A carrying a primary amine function a secondary amine function and a tertiary amine function, R4: for z = 0, is a C1 to C4 alkyl when said compound amine A) carries a secondary amine function and optionally a tertiary amine function, otherwise when said amine compound A) carries a primary amine function, in this case R4: - [CH2CH2-CO2] y-R5- (CO2-CH = CH2 ) (ny) or R4: at least in part is -CH2CH2-CC> 2-R'5 when there is presence of R radical monofunctional acrylate In addition to the multifunctional acrylate, with R'5 possibly comprising a free hydroxyl group, R'4: - [CH2CH2-CO2] y -R5- (CO2-CH = CH2) (ny) when z = 1 signifying presence simultaneous of a primary amine function with a secondary R5: residue of said multifunctional acrylate compound B selected in particular from the residues of polyethers, polyesters or polyurethane residues based on polyesters and polyether polyols, x = 1 if the amine A carries a tertiary amine function and x = 0 if there is no such tertiary amine function z = 1 if presence of secondary amine function at the same time as the primary amine function in the amine compound A) and z = 0 if there is no secondary amine function n: initial functionality of said acrylate B ranging from 1 to 6, preferably from 1 to 4, y: number of aminoacrylate groups created by addition reactions of an NH of said amine compound A on an acrylate group of said Acrylat e B, with 'y' ranging from 1 to 6, preferably from 1 to 4, and n-y: from 0 to 3 and preferably from 0 to 2, represents the number of residual acrylate groups in said P oligomer.
[14" id="c-fr-0014]
14. Oligomer according to one of claims 1 to 13, characterized in that said amine compound A) is an amine compound according to A1) as defined in claim 1 or 2 and that said acrylate compound B) comprises at least one compound multifunctional acrylate according to B1) and at least one monofunctional acrylate compound according to B2) and preferably said multifunctional acrylate compound according to B1) is a multifunctional partial or complete ester of at least one polyether polyol or of at least one polyol derived from said polyether with acrylic acid and that said monofunctional acrylate compound according to B2) is a monoester of acrylic acid of at least one polyether diol or monool or at least one diol or monool derivative of said polyether, more particularly said polyethers having a mass number average molecular weight Mn less than 2000 and preferably less than 1000.
[15" id="c-fr-0015]
15. Oligomer according to one of claims 1 to 13, characterized in that said amine compound A) is an amine compound according to A2) as defined in claim 1 or 2 and preferably said acrylate compound B) is an acrylate compound multifunctional according to B1) selected from partial or complete esters by acrylic acid of a polyether polyol or a polyol derived from said polyether, or from urethanes acrylates from a polyether polyol or from epoxy acrylates from a glycidyl polyether, more particularly said polyethers being polyoxyethylenes and having a number average molecular weight Mn less than 2000 and preferably less than 1000.
[16" id="c-fr-0016]
16. Oligomer according to one of claims 1 to 15, characterized in that said oligomer carries as ethylenic unsaturation acrylate groups with functionality in acrylate groups, including ammonium acrylate if acrylic acid is used as carboxylic acid compound C), ranging from 1 to 6, preferably from 1 to 4, more preferably from 1 to 3.
[17" id="c-fr-0017]
17. Oligomer according to one of claims 1 to 16, characterized in that it has a saline tertiary amine function level ranging from 0.1 to 25, preferably from 0.5 to 15 mEq per g of said oligomer.
[18" id="c-fr-0018]
18. Oligomer precursor of the oligomer as defined according to one of claims 1 to 13, in particular according to claim 13, characterized in that it comprises or is an oligomer according to formula (I) as defined according to claim 13.
[19" id="c-fr-0019]
19. Oligomer solution in a reactive diluent characterized in that it comprises the oligomer as defined according to one of claims 1 to 18 and at least one reactive diluent D) selected from mono (meth) acrylates and / or the multifunctional (meth) acrylates, preferably with D) being a (meth) acrylate of a polyether monool or polyol or a polyether monool or polyol derivative, of number average molecular weight less than or equal to 600.
[20" id="c-fr-0020]
20. Process for the preparation of an oligomer as defined according to one of claims 1 to 18, characterized in that it comprises the following successive stages: i) preparation of said precursor oligomer P by the addition of at least one amine compound A), according to A1) and / or according to A2) as defined according to claim 1 or 2, on B) an acrylate compound from: - B1) at least one multifunctional acrylate having a functionality ranging from 2 to 6 and preferably from 2 to 4, more preferably from 2 to 3, even more preferably from 2, when said amine compound A) is a compound according to A2) as defined according to claim 1 or 2, or - a mixture of at least one acrylate multifunctional according to B1) as defined above and at least one monofunctional acrylate according to B2), when said amine compound A) is an amine compound according to A1, as defined according to claim 1 or 2, this to block by the aminoacrylate formed one of two g -NH portions of said primary amine function of said amine compound according to A1), with the following molar ratios between groups: (acrylate) / (-NH)> 1 so that at least one residual acrylate group is carried by the product of addition i), which is said precursor oligomer P and in the case where said amine compound A) is according to A1 and said acrylate B) is a multifunctional acrylate mixture according to B1) and monofunctional acrylate according to B2) with a molar ratio B2 / A1 = 1/1 ii) salification of said precursor oligomer P which is the product of the addition step i), in the form of ammonium carboxylate salt by said carboxylic acid compound C), as defined according to US Pat. one of claims 1, 4 to 7 and 9 to 11, preferably with a molar ratio between carboxy groups and tertiary amine functions (= N-) including tertiary amines among aminoacrylate groups, (carboxy) / (tertiary amine) ranging from 0.10 to 1.00, preferably e from 0.5 to 1.00 and more preferably from 0.5 to 0.99.
[21" id="c-fr-0021]
21. Polymerizable oligomer, in particular crosslinkable, characterized in that it is obtained by the process as defined according to claim 20.
[22" id="c-fr-0022]
22. Polymerizable composition, in particular crosslinkable, characterized in that it comprises as binder at least one oligomer as defined according to one of claims 1 to 18 or obtained by a process as defined in claim 20 or a solution such as as defined in claim 19.
[23" id="c-fr-0023]
23. A composition according to claim 22, characterized in that it is polymerizable, in particular crosslinkable, by: - radiation pathway, in particular UV, LED, laser, electron beam preferably UV, - thermal or peroxide pathway or hydroperoxide in the presence of an accelerator - dual pathway combining at least two of the aforementioned routes and preferably - by radiation, more preferably by the UV route.
[24" id="c-fr-0024]
24. Composition according to one of claims 22 or 23, characterized in that it is a polymerizable composition, in particular curable, for a temporary function material, preferably among coating in particular ink, varnish, adhesive, or among hydrogel or support material for 3D printing object layer by layer, more preferably coating, or support material for 3D printing object layer by layer, and even more preferably for printing object support material in 3D layer by layer.
[25" id="c-fr-0025]
25. Use of an oligomer as defined according to one of claims 1 to 18 or a solution as defined according to claim 19 or the oligomer obtained by a process as defined according to claim 20, as a polymerizable binder and in particular crosslinkable, optionally water-soluble, in polymerizable compositions and in particular crosslinkable, preferably under radiation.
[26" id="c-fr-0026]
26. Use according to claim 25, characterized in that it applies to a material with a temporary function, removable by washing with water alone or with a saline water or other aqueous solution, preferably having a pH> 7, more preferably> 8, in particular materials with a temporary function among coatings, hydrogels or a support material for 3D printing object layer by layer, more particularly coatings or support material for 3D printing object layer by layer.
[27" id="c-fr-0027]
27. Use according to claim 25 or 26, characterized in that it applies to the printing of 3D objects by polymerization, in particular radiation crosslinking layer by layer of a composition comprising said oligomer or said oligomer solution as material with a temporary function of supporting or consolidating or molding said final 3D object, obtained after removal of said temporary function material by washing with water or with a saline solution or with another aqueous solution.
[28" id="c-fr-0028]
28. Polymeric material, in particular crosslinked, characterized in that it results from the use as polymerizable binder, in particular crosslinkable of at least one oligomer as defined in one of claims 1 to 18 or an oligomer obtained by the process as defined according to claim 20, an oligomer solution as defined according to claim 19 or the polymerization, in particular crosslinking, of a polymerizable composition, in particular crosslinkable, as defined according to one of claims 22 to 25.

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同族专利:

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公开号 | 公开日

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CN108137948B|2020-06-23|

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US20180298217A1|2018-10-18|

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WO2017060638A1|2017-04-13|

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EP3359607A1|2018-08-15|

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ES2796574T3|2020-11-27|

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CN108137948A|2018-06-08|

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US11021619B2|2021-06-01|

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EP3359607B1|2020-03-25|

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FR3042195B1|2017-11-24|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

US5030747A|1989-03-23|1991-07-09|Bayer Aktiengesellschaft|Process for the preparation of μ-amino-acrylic acid esters|

---

US5792827A|1994-01-13|1998-08-11|Basf Lacke + Farben, Ag|Addition products, radiation-curable surface coating compositions based on the addition products and their use for woodcoating and papercoating|

---

CA2239439A1|1995-12-04|1997-06-12|Basf Coatings Aktiengesellschaft|Methods of producing aqueous radiation-hardened paints|

---

US20120157351A1|2010-12-16|2012-06-21|Webber Peter A|Composition and method for reducing hydrate agglomeration|

---

US20130090444A1|2011-10-05|2013-04-11|Arkema France|Polar, multi-hydroxyl functional amino compounds, compositions, process for preparation, their uses & applications|

---

DE19545124A1|1995-12-04|1997-06-05|Basf Lacke & Farben|Radiation-curable water-based paints with a matt effect|

---

US8481241B2|2000-03-13|2013-07-09|Stratasys Ltd.|Compositions and methods for use in three dimensional model printing|

---

US7008998B2|2001-11-16|2006-03-07|Basf Corporation|Method for making an aqueous dispersion|

---

JP2005154549A|2003-11-25|2005-06-16|Seiko Epson Corp|Water-based ink composition and inkjet printing method using the same, and printed matter|

---

WO2005108513A1|2004-05-07|2005-11-17|Cytec Surface Specialties, S.A.|Radiation curable low gloss powder coating compositions|

---

CN101040002B|2004-08-30|2011-08-17|信越聚合物株式会社|Conductive composition and conductive crosslinked material, capacitor and method for manufacturing same, antistatic coating composition, antistatic coat, antistatic film, optical filter and optical information recording medium|

---

DE102005006296A1|2005-02-11|2006-08-24|Degussa Ag|Aqueous compositions|

---

US8470231B1|2009-06-01|2013-06-25|Stratasys Ltd.|Three-dimensional printing process for producing a self-destructible temporary structure|

---

EP2348089A1|2010-01-26|2011-07-27|S.P.C.M. Sa|Water-soluble polymers for oil recovery|

---

GB201005060D0|2010-03-25|2010-05-12|Davidson Robert S|Synergists|

---

JP5890990B2|2010-11-01|2016-03-22|株式会社キーエンス|Model material for optical modeling product formation, support material for shape support during optical modeling of optical modeling product, and manufacturing method of optical modeling product in inkjet optical modeling method|

---

CN103443146B|2011-03-25|2016-08-17|树脂核动力工业有限公司|Water-based paint compositions|

---

IN2014CN03889A|2011-10-28|2015-10-16|Basf Se|

---

US20140094558A1|2012-09-28|2014-04-03|Jeen International Corporation|Low Energy, Cold Process Formulation Aid|

---

CN104327593B|2014-11-18|2016-09-07|广州双科新材料有限公司|A kind of UV solidifies peelable ink and production method, construction method|

---

CN104526838B|2014-12-30|2017-01-11|宁波伏尔肯陶瓷科技有限公司|Method for 3D ceramic printing forming|

---

CN104860630A|2015-04-29|2015-08-26|肖先波|Environmental protection paint for building exterior wall|EP3353244B1|2015-12-02|2021-09-01|Sun Chemical Corporation|Polymeric aminoacrylates|

---

EP3401370A1|2017-05-10|2018-11-14|Allnex Belgium S.A.|Amino acrylates|

---

CN111647336A|2020-07-08|2020-09-11|镧明材料技术有限公司|Nano rare earth radiation-proof composite coating and preparation method thereof|

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2020-09-14| PLFP| Fee payment|Year of fee payment: 6 |

优先权:

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申请号 | 申请日 | 专利标题

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FR1559638A|FR3042195B1|2015-10-09|2015-10-09|IONIC OLIGOMER AND POLYMERIZABLE COMPOSITION CONTAINING THE SAME FOR HYDRO-FRAGMENTABLE MATERIALS FOR PROVISIONAL USE|FR1559638A| FR3042195B1|2015-10-09|2015-10-09|IONIC OLIGOMER AND POLYMERIZABLE COMPOSITION CONTAINING THE SAME FOR HYDRO-FRAGMENTABLE MATERIALS FOR PROVISIONAL USE|

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CN201680058645.8A| CN108137948B|2015-10-09|2016-10-06|Ionic oligomers and polymerizable compositions containing same for temporary use of water-cleavable materials|

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PCT/FR2016/052583| WO2017060638A1|2015-10-09|2016-10-06|Ionic oligomer, and polymerizable composition containing same for temporary-use water-fragmentable materials|

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ES16788178T| ES2796574T3|2015-10-09|2016-10-06|Ionic oligomer and polymerizable composition containing it for hydro-fragmentable materials for temporary use|

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US15/766,862| US11021619B2|2015-10-09|2016-10-06|Ionic oligomer and polymerizable composition containing same for temporary-use water-fragmentable materials|

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EP16788178.8A| EP3359607B1|2015-10-09|2016-10-06|Ionic oligomer, and polymerizable composition containing same for temporary-use water-fragmentable materials|