Process for modifying polymers
Process for modifying a polymer comprising the steps of (a) mixing the polymer with a maleimide-functionalized mono-azide and/or a citraconimide-functionalized mono-azide at a temperature in the range 80-250° C. to form a functionalized polymer, and (b) reacting the functionalized polymer with a substance containing one or more functional groups that can react with a maleimide or citraconimide functional group.
1. Process for modifying a polymer comprising the steps of
a) mixing said polymer with a maleimide-functionalized mono-azide and/or a citraconimide-functionalized mono-azide at a temperature in the range 80-250° C. to form a functionalized polymer, and
b) reacting the functionalized polymer with a substance containing one or more functional groups that can react with a maleimide or citraconimide functional group.
2. Process according to claim 1 wherein said substance contains at least two functional groups that can react with a maleimide or citraconimide functional group.
3. Process according to claim 1 wherein the reaction between the functionalized polymer with the substance containing one or more functional groups that can react with a maleimide or citraconimide functional group involves a Michael addition reaction or a Diels-Alder cycloaddition reaction.
4. Process according to claim 1 wherein the one or more functional groups are selected from the group consisting of amine, thiol, furan, and sorbate ester groups.
5. Process according to claim 2 wherein the substance containing at least two functional groups that can react with a maleimide or citraconimide functional group is selected from the group consisting of aminoalcohols, aminoacids, polyether monoamines, furans, aminofunctional silanes, mercaptoacids, and mercaptoalcohols.
6. Process according to claim 2 wherein the substance containing at least two functional groups that can react with a maleimide or citraconimide functional group is selected from the group consisting of 1,2,6-hexanetriol trithioglycolate, 1,3,5-trithiocyanuric acid, trimethylolpropane tris(3-mercaptopropionate), trimethylolpropane trithioglycolate, pentaerythritol tetrakis(3-mercaptopropionate), pentaerythritol tetrakisthioglycolate, pentaerythritol hexakis(3-mercaptopropionate), and pentaerythritol hexakisthioglycolate.
7. Process according to claim 2 wherein the substance containing at least two functional groups that can react with a maleimide or citraconimide functional group is selected from the group consisting of bis(hexamethylene)triamine, 1,6-diaminohexane, isophorone diamine, tris(2-aminoethyl)amine, 4-aminophenylether, bis(hexamethylene)triamine, and tris(2-aminoethyl)amine.
8. Process according to claim 2 wherein the substance containing at least two functional groups that can react with a maleimide or citraconimide functional group is selected from the group consisting of 2,2-di(2-furyl)propane, difurfurylsulfide, 2,2-di(2-furyl)propane, thiodimethylenedifuran, and ethane-1,2-diyl (2E,2′E,4E,4′E)-bis(hexa-2,4-dienoate).
9. Process according to claim 2 wherein the substance containing at least two functional groups that can react with a maleimide or citraconimide functional group is selected from the group consisting of pentaerythritol tetrakis(3-mercaptopropionate), bis(hexamethylene)triamine, tris(2-aminoethyl)amine, 2,2-di(2-furyl)propane, and difurfurylsulfide.
10. Process according to claim 1 wherein the polymer is an elastomer.
11. Process according to claim 10 wherein the elastomer is selected from the group consisting of natural rubber (NR), styrene butadiene rubber (SBR), butadiene rubber (BR), butyl rubber (IIR), ethylene propylene copolymer elastomer (EPM), ethylene propylene diene terpolymer elastomer (EPDM), and ethylene vinylacetate copolymer (EVA).
12. Process according to claim 1 wherein the polymer is a polyolefin.
13. Process according to claim 12 wherein the polyolefin is selected from the group consisting of polyethylene, polypropylene, and polyolefin elastomers.
14. Process according to claim 1 wherein the maleimide-functionalized azide has the following structure:
wherein Y is
m is 0 or 1, n is 0 or 1, n+m=1 or 2, R is selected from the group consisting of hydrogen, linear and branched alkyl groups with 1-6 carbon atoms optionally substituted with O, S, P, Si, or N-containing functional groups, alkoxy groups with 1-6 carbon atoms, and halogens, and X is a linear or branched, aliphatic or aromatic hydrocarbon moiety with 1-12 carbon atoms, optionally containing heteroatoms.
15. Process according to claim 1 wherein the citraconimide-functionalized azide has the following structure:
wherein Y is either
m is 0 or 1, n is 0 or 1, n+m=1 or 2, R is selected from the group consisting of hydrogen, linear and branched alkyl groups with 1-6 carbon atoms optionally substituted with O, S, P, Si, or N-containing functional groups, alkoxy groups with 1-6 carbon atoms, and halogens, and X is a linear or branched, aliphatic or aromatic hydrocarbon moiety with 1-12 carbon atoms, optionally containing heteroatoms.
16. Process according to claim 1 wherein the mono-azide is selected from the group consisting of 4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzenesulfonyl azide, 4-(3-methyl-2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzene sulfonyl azide, and 2-(3-methyl-2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl carbonazidate.