Multifunctional acrylic ether-ester products modified with carboxylic anhydride or its polyacid form, process for preparing same and associated crosslinkable compositions

US10501402B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10501402-B2
Application numberUS-201515523129-A
CountryUS
Kind codeB2
Filing dateOct 13, 2015
Priority dateOct 29, 2014
Publication dateDec 10, 2019
Grant dateDec 10, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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The invention also relates to a process for preparing said product, to crosslinkable compositions comprising same and to the use thereof in coatings, sealing, moulding or composite compositions, chemical sealing compositions, 3D printing compositions or compositions for 3D objects produced layer-by-layer. One particular advantage of these compositions is their low shrinkage despite their high functionality.

First claim

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The invention claimed is: 1. Multifunctional acrylated product having a number-average functionality f greater than 2.1 acrylic groups per mole of said product and with a density of said acrylic groups DA ranging from 2 to 12 mmol per g of said product, said product being the product of reaction by esterification and by etherification, by Michael addition reaction, between: a) a polyol R(OH) m or a mixture of polyols R(OH) m , of functionality m of at least 3 for a single polyol present and a number-average OH functionality greater than 2.1 for a mixture of said polyols, and b) the acrylic acid represented by R 1 OH, said reaction between a) and b) taking place in the presence of c) at least one cyclic carboxylic anhydride or of its polycarboxylic acid form R 2 (CO 2 H) z , of carboxy group (—CO 2 H) functionality z of at least 2 and ranging up to 4: the ratio r 1 of number of carboxy groups of said anhydride c) relative to those of b) acrylic acid, r 1 =(CO 2 H) c /(CO 2 H) b ranging from 0.01 to 0.4, the carboxy groups being overall in stoichiometric deficit relative to the hydroxyl groups of said polyol a), with r=CO 2 H/OH<1, wherein: R is the residual radical of a polyol of valency m or a mixture of polyols of valency m; R 1 is an acryloyl radical; and R 2 is the residue of valency z of said at least one cyclic carboxylic anhydride or of its polycarboxylic acid form; said acrylic product comprising in its composition both: units A) of oligoether-ester acrylate that are derived from the reaction of a) and of b), formed by a Michael addition reaction: of the OH groups of said polyol a) or of OH groups of hydroxylated partial acrylates formed on the unsaturation of the acrylic acid b) or on the unsaturation of one of the acrylates formed by esterification with b) and simultaneous esterification with b) of said polyol a) and of said b hydroxylated partial acrylates or simultaneous esterification with the carboxy groups of the carboxylated Michael adduct formed between a) and b), and units B) of oligoester acrylates derived from c) by a reaction of esterification with said anhydride or with its polyacid form c) of said polyol a) or of said hydroxylated partial acrylates or of the hydroxylated ether-ester acrylates formed, said acrylic product being a mixture of acrylic products comprising at least one acrylic product (p1) chemically linking, in its molecular structure, the units A) and B) as defined above, wherein the product has an overall composition represented by the following average general formula (I): R 1 O-[[A] a -[B] b ] n —R(OR 1 ) m-1   (I) with a and b representing the average mole fraction of each unit A) and B) per overall average unit of said product and with a+b=1 and a/b ranging from 0.15 to 22, n being the number of repeat overall units, with average n per mole of product n ave ranging from 0.2 to 10. 2. The product of claim 1 , wherein the product comprises said product p1 and that said product p1 has a molecular structure defined according to general formula (II) below: (R 1 O) m-1 —R—[—[O—CH 2 CH 2 —CO 2 —R(OR 1 ) m-2 ] a [O 2 C—R 2 (CO 2 X) z-2 —CO 2 —R(OR 1 ) m-2 ] b ] n —OR 1    (II) and with the presence of at least four products having a different n, corresponding to n=0 and n=1, n=2 and n=3 with: R 1 being the acryloyl radical, R being the residual radical of said polyol R(OH) m or representing an average radical of a mixture of polyols, R 2 being the residue of valency z of said anhydride or its polycarboxylic acid form and X being —R(OR 1 ) m-1 with X possibly being more than 95%, —R(OR 1 ) m-1 and the rest less than 5% of X being H, with an acid number not exceeding 15 mg KOH/g, n being the number of repeat units and a and b being the respective mole fractions of the particular units in the overall repeat unit with the ratio a/b ranging from 0.15 to 22. 3. The product of claim 1 wherein it comprises, in addition to said product p1, the oligoether-ester acrylate product p2 based on units A) of general formula (III) below: (R 1 O)—[—R[OR 1 ] m-2 —O—(C═O)—CH 2 —CH 2 —O—] n —R—(OR 1 ) m-1   (III) with the presence of at least four products having a different n and corresponding to n=0 and n=1, n=2 and n=3 and n being the number of repeat units. 4. The product of claim 1 wherein it comprises, in addition to said product p1, the oligoester acrylate product p3 of general formula (IV) below: (R 1 O)—[—R[OR 1 ] m-2 —O—(C═O)—R 2 (C═O)O—] n —R—(OR 1 ) m-1   (IV) with the presence of at least four products having a different n and corresponding to n=0 and n=1, n=2 and n=3 and n being the number of repeat units. 5. The product of claim 4 , wherein it comprises a product p2 as defined according to formula (III) of claim 3 , said product p1 is as defined according to formula (II) of claim 2 and the three products p1, p2 and p3 thus defined each comprise at least a fifth product corresponding to n=4 and, optionally, an additional product corresponding to n=5. 6. The product of claim 1 to 5 , wherein said product p1 has the following general formula (V): (R 1 O)—[—R[OR 1 ] m-2 —O 2 C—CH 2 —CH 2 —O—] n —R—(OR 1 ) m-2 —O 2 C—R 2 (CO 2 —X 1 ) z-2 —CO 2 —X 2   (V) with R 2 being the radical having valency z corresponding to said carboxylic anhydride or to said polycarboxylic acid and X 1 and X 2 possibly being identical or different and chosen from: —R(OR 1 ) m-1 or —R(OR 1 ) m-2 —[O—CH 2 —CH 2 —CO 2 —R(OR 1 ) m-2 ] n —(OR 1 ) or in part H or in part the residue of a reactive blocking agent chosen from a monofunctional reactive blocking agent, reactive with the carboxy group. 7. The product of claim 1 wherein the overall molecular distribution in terms of n of said product is such that it represents at least 80% by weight for n ranging from 0 to 4 and no more than 20% by weight of said distribution for n being greater than 4, with a number-average weight Mn of said product, measured by GPC in THF and expressed in polystyrene equivalents, ranging from 500 to 10000. 8. The product of claim 1 wherein said polyol a) has a functionality m for polyol a) alone of at least 3 and that said product comprises linear oligoether-ester acrylate products p2 according to general formula (III) and also at least one oligoether-ester acrylate product of branched structure. 9. Acrylated product, wherein it can be obtained by simultaneous or successive and alternating reactions between a) a polyol R(OH) m or a mixture of polyols R(OH) m , having a functionality m of at least 3 for a polyol a) alone, or having a number-average functionality with respect to m greater than 2.1 for a mixture of polyols R(OH) m and b) the acrylic acid (R 1 OH) in stoichiometric deficit relative to a), and in the presence of c) at least one cyclic carboxylic anhydride or of its polyacid form having a carboxy group functionality z ranging from 2 to 4, with an overall ratio r=CO 2 H/OH of less than 1 with r 1 being the ratio of the carboxy groups of c) to the carboxy groups of b) acrylic acid, r 1 =(carboxy) c /(carboxy) b , wherein R is the residual radical of a polyol of valency m or a mixture of polyols of valency m and R 1 is an acryloyl radical. 10. The product of claim 1 wherein said polyol a) is selected from polyol monomers and/or polyol oligomers with Mn for polyol oligomers not exceeding 700. 11. The product of claim 10 , wherein said polyol is a polyol monomer and selected from: diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, tetrapropylene glycol, butanediol, neopentyl glycol, hexanediol, isosorbide, glycerol, trimethylolpropane, pentaerythritol, ditrimethylol

Assignees

Inventors

Classifications

  • of alcohol terminated polyesters or polycarbonates, e.g. polyester (meth)acrylates · CPC title

  • of polyhydric alcohols or polyhydric phenols, e.g. ethylene glycol dimethacrylate · CPC title

  • in which at least one of the two components contains aliphatic unsaturation · CPC title

  • C09D4/06Primary

    {Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond} in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00 · CPC title

  • C08G63/668Primary

    derived from polycarboxylic acids and polyhydroxy compounds · CPC title

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What does patent US10501402B2 cover?
The invention also relates to a process for preparing said product, to crosslinkable compositions comprising same and to the use thereof in coatings, sealing, moulding or composite compositions, chemical sealing compositions, 3D printing compositions or compositions for 3D objects produced layer-by-layer. One particular advantage of these compositions is their low shrinkage despite their high f…
Who is the assignee on this patent?
Arkema France
What technology area does this patent fall under?
Primary CPC classification C09D4/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).