Method for producing functionalized thermoplastic elastomers

Patent metadata

Field	Value
Publication number	US-10189933-B2
Application number	US-201414772023-A
Country	US
Kind code	B2
Filing date	Mar 14, 2014
Priority date	Mar 20, 2013
Publication date	Jan 29, 2019
Grant date	Jan 29, 2019

Abstract

A method for producing functionalized thermoplastic elastomers on the basis of grafting substrates, selected from olefine-block copolymers of composition 80 to 98 mass-% ethylene-/2 to 20 mass-% C3- to C12-olefine units or partially crystalline propylene/ethylene and/or C4- to C12-olefine and/or C4- to C12-diene-copolymers of composition 50 to 98 mass-% propylene-/2 to 50 mass-% C2- and/or C4- to C12-olefine and/or C4- to C12-diene units or cross-linked styrene/olefine/styrene or styrene/olefine-block copolymers, wherein, in a liquid mixing reactor per 100 mass parts of particular grafting substrate—0.1 to 15 mass parts of at least one functional monomer from the series of functional groups comprising α,β-ethylenic unsaturated compounds or 0.1 to 15 mass parts of a monomer mixture comprising at least one of said functional monomers and—0.01 to 10 mass parts of at least one initiator forming free radicals having a 1-hour half-life temperature (THwz/1h) between 50 and 200° C. are added and, at reaction temperatures between 40° C. and the melting or softening temperature of the grafting substrate, are polymerized over a reaction period between 10 and 200 min to solid-fluid phase, wherein a grafting product having a grafted functional monomer is produced by such a solid phase functionalization which is used as an input component for further processing. Functionalized thermoplastic elastomers having a degree of functionalization between 0.1 and 5 mass-% can be obtained using the method. Said elastomers are suitable for use as a bonding agent and/or adhesive agent for various substrates or multi-layer composites.

First claim

The invention claimed is:

1. A process for preparing a functionalized thermoplastic elastomer based on particulate graft substrates selected from the group consisting of:
(i) olefin block copolymers comprising 80 to 98 mass-% of ethylene- and 2 to 20 mass-% of C 3 - to C 12 -olefin units;
(ii) semi-crystalline copolymers of the composition 50 to 98 mass-% of propylene- and 2 to 50 mass-% of ethylene and/or C 4 - to C 12 -olefin and/or C 4 - to C 12 -diene units, and
(iii) cross-linked styrene/olefin/styrene block copolymers or cross-linked styrene/olefin block copolymers,
wherein in a fluid mixing reactor, is added:
0.1 to 15 mass parts of α,β-ethylenically unsaturated compounds containing at least one functional monomer or a monomer mixture containing the at least one functional monomer, wherein the at least one functional monomer contains functional groups,
0.01 to 10 mass parts of at least one initiator forming free radicals with a 1-hour half-life temperature (T HWZ/1h ) between 50 and 200°, and
100 mass parts of the particulate graft substrate;
wherein the unsaturated compounds, the at least one initiator and particulate graft substrate are polymerized at reaction temperatures between 40° C. and the melting or softening temperature of the particulate graft substrate for a reaction time between 10 and 200 min in a solid-fluid phase, wherein a graft product having a grafted functional monomer is produced by such a solid state functionalization, which is used as a starting component for further processing, wherein during further processing:

100 mass parts of the graft product is mixed with: (i) between 0.1 and 60 mass parts of at least one other functional monomer; or (ii) between 0.1 and 60 mass parts of another monomer mixture containing the at least one other functional monomer and between 0.01 and 20 mass parts of at least one other initiator forming free radicals with a 1-hour half-life temperature (T HWZ/1h ) 80-240° C. producing a mixture; the mixture together with 100 to 4000 mass parts of an unmodified olefin elastomer, are continuously fed into an intake area of a reaction extruder via metering devices,
reactive extrusion from the reactor extruder is carried out at temperatures above melting or softening point of the unmodified olefin elastomer, and
the functionalized thermoplastic elastomer is continuously discharged from the reaction extruder.

2. The process according to claim 1 , wherein the at least one functional monomer is α,β-ethylenically unsaturated compounds containing carboxyl groups and/or derivatives selected from their anhydrides and/or mono- or diesters and/or mono- or diamides.

3. The process according to claim 1 , wherein the functional groups comprise hydroxyl, epoxy-, amino-, imido- or silane groups.

4. The process according to claim 2 , wherein the functional monomers are maleic anhydride (MA) and/or acrylic acid (AS) alone or as a mixture with a co-monomer from a group of vinyl aromatics.

5. The process according to claim 2 , wherein the functional monomers are C 1 - to C 12 -alkyl esters of acrylic or methacrylic acid alone or as a mixture with a co-monomer from a group of vinyl aromatics.

6. The process according to claim 4 , wherein compositions of 99 to 20 mass-% of the functional monomer and 1 to 80 mass-% of the co-monomer are used.

7. The process according to claim 1 , wherein the radical-initiated grafting using a radical former or a mixture consisting of at least two different free-radical formers is performed using organic peroxides with 1-hour half-life temperature (T HWZ/1h ) between 50 and 200° C. or a 1-minute half-life temperature (T HWZ/1min ) between 85 and 250° C. in a concentration between 0.001 and 5 mass-% in relation to an entire quantity of the graft substrate.

8. The process according to claim 7 , wherein dialkyl peroxydicarbonates with a 1-hour half-life temperature (T HWZ/1h ) between 60 and 70° C., dilauroylperoxide (DLPO) with a 1-hour half-life temperature (T HWZ/1h ) of 80° C., dibenzoyl peroxide (DBPO) with a 1-hour half-life temperature (T HWZ/1h ) of 91° C., tert-butyl peroxy-2-ethylhexanoate (TBPEH) with a 1-hour half-life temperature (T HWZ/1h ) of 91° C., tert-butyl peroxy-isobutyrate (TBPIB) with a 1-hour half-life temperature (T HWZ/1h ) of 98° C., 1,1-di-(tert-butylperoxy) cyclohexane (DTBPC) with a 1-hour half-life temperature (T HWZ/1h ) of 113° C., tert-butyl perbenzoate (TBPB) with a 1-hour half-life temperature (T HWZ/1h ) of 122° C., dicumyl peroxide (DCP) having a 1-hour half-life temperature (T HWZ/1h ) of 132° C., 2,5-dimethyl-2,5-di (tert-butylperoxy) hexane (DHBP) with a 1-hour half-life temperature (T HWZ/1h ) of 134° C., 2,5-dimethyl-2,5-di (tert-butylperoxy) hexyne-3 (DYBP) with a 1-hour half-life temperature (T HWZ/1h ) of 141° C., di-tert-butyl peroxide (TBP) having a one-hour half-life temperature (T HWZ/1h ) of 141° C., cumene hydroperoxide (CHP) with a 1-hour half-life temperature (T HWZ/1h ) of 166° C. and tert-butyl hydroperoxide (TBHP) with a 1-hour half-life temperature (T HWZ/1h ) of 185° C. are used as the radical formers.

9. The process according to claim 1 , further comprising the step of adding to the functionalized thermoplastic elastomer at least one additive selected from antioxidants and/or processing stabilizers, fillers, reinforcement agents, flame retardants, lubricants, extender oils, and at least one polymer and/or elastomer component with a proportion of 1 to 90 mass-% based on the entire elastomeric extruded mass.

10. The process according to claim 9 , further comprising the step of adding as processing stabilizers primary antioxidants which are sterically hindered phenol compounds with a proportion of 0.01 to 5 mass parts in relation to an elastomeric olefin copolymer or olefin block copolymer functionalized to 100 mass parts.

11. The process according to claim 10 , wherein the processing stabilizers are a combination of at least one primary and at least one secondary antioxidant.

12. The method according to claim 1 , wherein the fluid mixing reactor is a temperature-controllable mixer for fine-grained materials.

13. A process for preparing a functionalized thermoplastic elastomer based on particulate graft substrates selected from the group consisting of:
(i) olefin block copolymers comprising 80 to 98 mass-% of ethylene- and 2 to 20 mass-% of C 3 - to C 12 -olefin units;
(ii) semi-crystalline copolymers of the composition 50 to 98 mass-% of propylene- and 2 to 50 mass-% of ethylene and/or C 4 - to C 12 -olefin and/or C 4 - to C 12 -diene units, and
(iii) cross-linked styrene/olefin/styrene block copolymers or cross-linked styrene/olefin block copolymers,
wherein in a fluid mixing reactor is added:
0.1 to 15 mass parts of α,β-ethylenically unsaturated compounds containing at least one functional monomer or a monomer mixture containing the at least one functional monomer, wherein the at least one functional monomer contains functional groups,
0.01 to 10 mass parts of at least one initiator forming free radicals with a 1-hour half-life temperature (T HWZ/1h ) between 50 and 200° C. are added to, and
100 mass parts of the particulate graft substrate;
wherein the unsaturated compounds, the at least one initiator and the particulate graft substrate are polymerized at reaction temperatures between 40° C. and the melting or softening temperature of the particulate graft substrate for a reaction time between 10 and 200 min in a solid-fluid phase, wherein a graft product having a grafted functional monomer is produced by such a solid state functionalization, which is used as a starting component for further processing, wherein during further process

Assignees

• Byk Kometra Gmbh
• Byk Chemie Gmbh

Inventors

• Besser Klaus Dieter
• Gerecke Jochen
• Leitner Bianka
• Rapthel Inno

Classifications

• C09J151/003

  grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds (C09J151/04, C09J151/06 take precedence) · CPC title

• C08F2/36

  Polymerisation in solid state · CPC title

• C08F4/38

  Mixtures of peroxy-compounds · CPC title

• C08F287/00 Primary

  Macromolecular compounds obtained by polymerising monomers on to block polymers · CPC title

• C08K5/52

  Phosphorus bound to oxygen only · CPC title