Method for curing curable compositions

Patent metadata

Field	Value
Publication number	US-2018148554-A9
Application number	US-201515515884-A
Country	US
Kind code	A9
Filing date	Aug 6, 2015
Priority date	Oct 1, 2014
Publication date	May 31, 2018
Grant date	—

Abstract

The invention relates to a process for the curing of latently reactive, heat-curable compositions which do not harden at room temperature. The composition includes a polymer obtainable via reaction of certain compounds having two aldehyde groups with polyacrylate compounds having two or more acrylate groups, and also a compound which bears at least two thiol groups.

First claim

1 . A process for the curing of curable compositions the process comprising:
providing at least one heat-curable composition, and hardening the composition by heating to temperatures greater than or equal to 60° C., wherein the curable composition comprises:
(a) at least one polymer (S) obtainable via reaction of at least one compound having two aldehyde groups and of at least one acrylate compound (B) selected from the group consisting of acrylate compounds having more than two acrylate groups (By) and diacrylate compounds (B2),
wherein the at least one compound having two aldehyde groups is an aromatic dialdehyde having a molecular structure wherein the bonds to the two aldehyde groups are at an angle to one another, and
(c) at least one compound (C) which bears at least two thiol groups.

2 . The process according to claim 1 , wherein the curable composition exhibits a viscosity increase of less than 100 000 mPa s within a period of 4 h at room temperature.

3 . The process according to claim 1 , wherein the compound having two or more aldehyde groups is selected from the group consisting of phthalaldehyde, isophthalaldehyde, and a mixture of these.

4 . The process according to claim 1 , wherein the diacrylate compounds (B2) are difunctional acrylates of one of alkanediols, cycloalkanediols, lower polyalkylene glycols and diamines, and wherein the acrylate compounds (By) are selected from the group consisting of polyether acrylates, polyester acrylates, acrylated polyacrylatols, urethane acrylates, and acrylic esters of alkoxylated polyols.

5 . The process according to claim 1 , wherein the acrylate compounds (By) and (B2) are selected from the group consisting of ethylene glycol diacrylate, 1,2-propanediol diacrylate, 1,3-propanediol diacrylate, 1,3-butanediol diacrylate, 1,4-butanediol diacrylate, 1,5-pentanediol diacrylate, 1,6-hexanediol diacrylate, 1,8-octanediol diacrylate, neopentyl glycol diacrylate, 1,1-cyclohexanedimethanol diacrylate, 1,2-cyclohexanedimethanol diacrylate, 1,3-cyclohexanedimethanol diacrylate, 1,4-cyclohexanedimethanol diacrylate, 1,2-cyclohexanediol diacrylate, 1,3-cyclohexanediol diacrylate, 1,4-cyclohexanediol diacrylate, diethylene glycol diacrylate, dipropylene glycol diacrylate, tripropylene glycol diacrylate, N,N′-bisacryloyl-2,2-diaminoethane, N,N′-bisacryloyl-1,6-diaminohexane, N,N′-bisacryloylpiperazine, trimethylolpropane triacrylate, ditrimethylolpropane pentaacrylate, ditrimethylolpropane hexaacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, glycerol diacrylate, glycerol triacrylate, di- or polyacrylates of sugar alcohols, di- or polyacrylates of polyester polyols, di- or polyacrylates of polyetherols, di- or polyacrylates of polyTHF with molecular weight from 162 to 2000, di- or polyacrylates of poly-1,3-propanediol with molecular weight from 134 to 1178, di- or polyacrylates of polyethylene glycol with molecular weight from 106 to 898, urethane di- and polyacrylates and polycarbonate di- and polyacrylates.

6 . The process according to claim 1 , wherein the acrylate compound is a diacrylate compound (B2) and is selected from the group consisting of ethylene glycol diacrylate, 1,2-propanediol diacrylate, 1,3-propanediol diacrylate, 1,4-butanediol diacrylate, and 1,6-hexanediol diacrylate.

7 . The process according to claim 1 , wherein the at least one compound (C) having at least two thiol groups are one of compounds (C1) of the formula

or compounds (C2) of the formula

or compounds (C3) of the formula

in which
Z 1 , Z 2 , Z 3 , Z 4 , Z 5 and Z 6 are in each case mutually independently a single bond or a moiety of the formula —(C═O)—R 3 —S—,
R 3 is a divalent C 1 - to C 6 -alkylene moiety,
p, q, r, s, t, u are in each case mutually independently zero or a positive integer from 1 to 5,
each X i for i=from 1 to p, from 1 to q, from 1 to r, from 1 to s, from 1 to t and from 1 to u can be selected mutually independently from the group consisting of —CH 2 —CH 2 —O—, —CH 2 —CH(CH 3 )—O—, —CH(CH 3 )—CH 2 —O—, —CH 2 —C(CH 3 ) 2 —O—, —C(CH 3 ) 2 —CH 2 —O—, —CH 2 —CHVin-O—, —CHVin-CH 2 —O—, —CH 2 —CHPh-O— and —CHPh-CH 2 —O—,
wherein Ph is phenyl and Vin is vinyl,
wherein when the at least one compound (C) comprises compound (C1) at least four of the moieties Z 1 to Z 6 are a group of the formula —(C═O)—R 3 —S—, and wherein when the at least one compound (C) comprises one of compounds (C2) or (C3) at least three moieties Z 1 to Z 4 are a group of the formula —(C═O)—R 3 —S—.

8 . The process according to claim 1 , wherein the at least one compound (C) having at least two thiol groups are di- or trifunctional compounds (C4) of the formula

in which
R 1 and R 2 are in each case mutually independently hydrogen or a C 1 - to C 4 -alkyl moiety,
R 4 is methylene or 1,2-ethylene,
k, l, m, n are in each case mutually independently zero or a positive integer from 1 to 5
each Y i for i=from 1 to k, from 1 to l, from 1 to m, and from 1 to n can be selected mutually independently from the group consisting
of —CH 2 —CH 2 —O—, —CH 2 —CH(CH 3 )—O—, —CH(CH 3 )—CH 2 —O—, —CH 2 —C(CH 3 ) 2 —O—, —C(CH 3 ) 2 —CH 2 —O—, —CH 2 —CHVin-O—, —CHVin-CH 2 —O—, —CH 2 —CHPh-O— and —CHPh-CH 2 —O—, wherein Ph is phenyl and Vin is vinyl.

9 . The process according to claim 1 , wherein the at least one compound (C) is selected from the group consisting of ethylene glycol di(3-mercaptopropionate) (GDMP), trimethylolpropane tri(3-mercaptopropionate) (TMPMP), trimethylolpropane trimercaptoacetate (TMPMA), 3-mercaptopropionic ester of poly-1,2-propylene glycol with molar mass from 500 to 2500 g/mol, 3-mercaptopropionic ester of ethoxylated trimethylolpropane with molar mass up to 1500 g/mol, pentaerythritol tetra(3-mercapotopropionate) (PETMP), pentaerythritol tetramercaptoacetate (PETMA), dipentaerythritol tetra(3-mercaptopropionate), dipentaerythritol tetramercaptoacetate, dipentaerythritol penta(3-mercaptopropionate), dipentaerythritol pentamercaptoacetate, dipentaerythritol hexa(3-mercaptopropionate), dipentaerythritol hexamercaptoacetate, ditrimethylolpropane tetra(3-mercaptopropionate), ditrimethylolpropane tetramercaptoacetate, and alkoxylated products of these.

10 . The process according to claim 1 , wherein the curable composition further comprises a catalyst (E) which can accelerate the addition reaction between the thiol groups, wherein the catalyst (E) is selected from the group consisting of primary, secondary, and tertiary amines, primary, secondary, and tertiary phosphines, quaternary ammonium and phosphonium salts, imines, and iminium salts.

11 . The process according to claim 1 , wherein the process is selected from the group consisting of injection molding, injection-compression molding, flow molding, reaction injection molding (RIM), RTM (resin transfer molding), VARTM (vacuum assisted RTM), tape layup processes, coil coating, filament winding, manual lamination, pultrusion, hot reactive adhesive bonding, and high-temperature-hardening coating processes.

12 . The process according to claim 1 , wherein the curable composition comprises:
(a) from 10 to 80% by weight of the polym

Assignees

• Basf Se

Inventors

• Feichtenschlager Bernhard
• Smeets Alfons
• Bruchmann Bernd
• Thomas Hans-Josef
• Fleischel Olivier

Classifications

• C08J2361/00

  Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers · CPC title

• C09J133/064

  containing anhydride, COOH or COOM groups, with M being metal or onium-cation · CPC title

• C08J5/042 Primary

  with carbon fibres · CPC title

• C08J2367/06

  Unsaturated polyesters · CPC title

• C08J3/247 Primary

  Heating methods · CPC title