Method of reactive extrusion copolymerization of vinyl monomers

Patent metadata

Field	Value
Publication number	US-10689469-B2
Application number	US-201816157974-A
Country	US
Kind code	B2
Filing date	Oct 11, 2018
Priority date	Apr 11, 2016
Publication date	Jun 23, 2020
Grant date	Jun 23, 2020

Abstract

A method of reactive extrusion copolymerization of vinyl monomer consisting of (1) feeding vinyl monomer or at least one vinyl monomer together with an initiator into the first screw of twin-screw extruder, and modified resin into the subsequent screw section; (2) feeding the above monomer into the screw segment after auto-acceleration zone and feeding the initiator corresponding to the temperature of barrel and micro/nano inorganic modified fillers after the half-life period of the initiator; (3) feeding the antioxidant and anti-UV agent at the end of the polymerization, and then removing unpolymerized monomer and by-products by devolatilization of screw segment; (4) obtaining vinyl copolymer resin with a anticipated molecular weight of 5×102 to 6×105 from the reactive extrusion polymerization by controlling the temperature of different screw segments. The invention which overcomes the existing defects of the free radical polymerization by reactive extrusion technology, can not only meet the requirement of short stay time of reactive extrusion polymerization, combine the functionalization and high performance, but also make it possible to obtain high molecular weight polymers.

First claim

We claim:

1. A method of reactive extrusion copolymerization of vinyl monomers consisting of:
(1) feeding a vinyl monomer and/or at least one sort of vinyl comonomer and an initiator into a first screw segment of a twin-screw extruder, and feeding a modified resin into subsequent screw segments;
(2) feeding the vinyl monomer and/or vinyl comonomer into a screw segment after an auto-acceleration zone, and feeding the initiator corresponding to a temperature of a barrel and micro- or nano-scale inorganic modified fillers after the half-life period of the initiator;
(3) feeding antioxidants and anti-UV agents at the end of polymerization, and removing unpolymerized monomers and by-products by devolatilization of a screw segment; and
(4) obtaining a vinyl copolymer resin with an anticipated molecular weight of 5×10 2 to 6×10 5 from reactive extrusion copolymerization by controlling the temperature of different screw segments.

2. A method of reactive extrusion copolymerization of vinyl monomers consisting of:
(1) feeding a vinyl monomer or at least one kind of vinyl comonomer and an initiator into a first screw segment of a first twin-screw extruder, and feeding a modified resin into a subsequent screw segment;
(2) feeding an appropriate monomer into a screw segment behind an auto-acceleration zone, and feeding the initiator corresponding to a temperature of a barrel and micro- or nano-scale inorganic modified fillers after the half-life period of the initiator, and obtaining a prepolymer of vinyl copolymer;
(3) feeding the prepolymer of vinyl copolymer into a second twin-screw extruder, feeding vinyl monomer and initiator continuously and feeding an antioxidant and anti-UV agents at the end of polymerization, and removing unpolymerized monomers and by-products by devolatilization of a screw segment; and
(4) obtaining a vinyl copolymer resin with an anticipated molecular weight of 5×10 2 to 6×10 5 from reactive extrusion copolymerization by controlling the temperature of different screw segments.

3. The method according to claim 1 , wherein the twin-screw extruder includes a first twin-screw extruder and a second twin-screw extruder,
the first twin-screw extruder has a power inlet that can suffer at least 0.3 MPa pressure without leakage, or the first twin-screw extruder is a tight intermeshing twin-screw extruder with a structure of reverse direction flow; and
the second twin-screw extruder is a co- or counter-rotating twin screw equipped with a devolatilization section and an inert gas introduction unit which introduces an inert gas into the devolatilization section.

4. The method according to claim 2 , wherein the first twin-screw extruder has a power inlet that can suffer at least 0.3 MPa pressure; or the first twin-screw extruder is a tight intermeshing twin-screw extruder with a structure of reverse direction flow; and
the second twin-screw extruder is a co-rotating or counter-rotating twin-screw extruder equipped with a devolatilization section and an inert gas introduction unit which introduces an inert gas into the devolatilization section.

5. The method according to claim 1 , wherein the mass ratio of the modified resin to the sum of the vinyl monomer and the vinyl comonomer equals 0-30: 100-70;
the addition amount of the initiator is 0-20% of the amount of all vinyl monomers;
the addition amount of the nano- or micron-scale inorganic modified fillers equals 0-30% of the total mass of the vinyl monomer and the vinyl comonomer;
the mass ratio of the antioxidants to the anti-UV agents is from 2: 1 to 1: 2; and
the addition amount of the antioxidants and anti-UV agents equals to 0.1-1% of the total mass of reactants.

6. The method according to claim 1 , wherein the vinyl monomer or vinyl comonomer is one or several species selected from styrene, acetophenone, divinylbenzene, acrylonitrile, butadiene, isoprene, methacrylic acid, methylmethacrylate esters, ethyl methacrylate, butyl methacrylate, amyl methacrylate, hydroxyethyl methacrylate, β-hydroxypropyl methacrylate, cyclohexyl methacrylate, glycidyl methacrylate , acrylic acid, ethyl acrylate, butyl acrylate, pentyl acrylate, hydroxyethyl acrylate, β-hydroxypropyl acrylate, cyclohexyl acrylate, glycidyl acrylate, polycyclic norbornene methacrylate, dicyclopentenyl acrylate, phenyl methacrylate, p-chlorophenyl methacrylate, adamantyl methacrylate, isobornyl methacrylate, vinyl pyridine, maleic anhydride, maleic acid, maleic acid, maleic acid monoesters, maleic acid diesters, fumaric acid monoesters, fumaric acid diesters, N-methyl maleimide, N-cyclohexyl maleimide, N-phenyl maleimide, N-tolyl maleimide, N-o-chlorobenzene maleimide Itaconic acid, itaconic acid ester, sorbic acid, sorbic acid ester, tetrafluoroethylene, hexafluoroethylene, vinylidene fluoride, vinyl chloride, vinylidene chloride, vinyl isocyanate, and acryloyl chloride.

7. The method according to claim 1 , wherein the initiator is one or several species selected from inorganic peroxide, organic peroxide, azo initiator, and redox initiator,
wherein the inorganic peroxide consists of potassium persulfate, sodium persulfate or ammonium persulfate;
the general formula of the organic peroxide is R-O-O-R′, wherein R and R′ are selected from H, alkyl, acyl or carbonate, and R and R′ are same or different;
the azo initiator consists of azobisisobutyronitrile or azobisisobutyronitrile; and
the redox initiator consists of cumene hydroperoxide-ferrous salt or organic peroxide-aromatic tertiary amine system.

8. The method according to claim 1 , wherein the modified resin is one or several species selected from one or more of the group consisting of styrene butadiene rubber, nitrile rubber, natural rubber, styrene-butadiene-styrene triblock copolymer, styrene-isoprene-styrene triblock copolymer, hydrogenated styrene-butadiene-styrene triblock copolymer, hydrogenated styrene-isoprene-styrene triblock copolymer, a styrene/butadiene random copolymer thermoplastic elastomer, a methylmethacrylate-butylmethacrylate microdiblock copolymer material, methyl acrylate-butyl acrylate micron-sized diblock copolymer, methyl methacrylate-butyl acrylate micro/nano diblock copolymer, methyl methacrylate / butyl methacrylate random copolymer, methyl methacrylate/butyl acrylate random copolymer, styrene-butadiene-methyl methacrylate micro-nano triblock copolymer, styrene-isoprene-methyl methacrylate micro-nano triblock copolymer, thermoplastic polyurethane, and a polymer of the vinyl monomer and the vinyl comonomer.

9. The according to claim 1 , wherein the micro- or nano-scale inorganic modified fillers are at least one of the group consisting of micro/nano silica, micro/nano calcium carbonate, micro/nano aluminum oxide, micro/nano aluminum hydroxide, micro/nano magnesium hydroxide, micro/nano tantalum oxide, micro/nano whisker, micro/nano quartz, micro/nano oxide tetrahydrate, micro/nano europium oxide, micro/nano zirconia, micro/nano barium oxide, and micro/nano lanthanum oxide.

10. The method according to claim 1 , wherein the antioxidants are at least one compound selected from market-selling antioxidant 168, antioxidant 1076, antioxidant bht, antioxidant B215, antioxidant 245 or antioxidant 1010, thiodipropionic acid bis (octadecyl acrylate), Diphenyl isooctyl phosphite, tetrakis [methyl-β-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate] pentaerythritol, 1,3-tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butane, 1,1,3-tris (2-methyl-4- hydroxy-5-tert-butylphenol), 3,5-di-tert-butyl-4-hydroxyphenyl propionate ester, 2,2′-methylenebis (4-methyl-6-tert-butyl) phenol, 4′4- thiobis (6-tert-butyl-o-cresol), 4,4′-thiobis (3-methyl-6-tert-butyl) phenol, 4′4-(dihydroxy-3,3′, 5,5′-tetra-tert-butyl biphenyl); and anti-UV age

Assignees

• Univ East China Science & Tech
• Shanghai Fuyuan Rubber And Plastic Tech Ltd

Inventors

• Zheng Anna
• Guan Yong
• Wei Dafu
• Xu Xiang
• Zhan Pengfei
• Liu Weixing
• Shi Han

Classifications

• C08F287/00

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

• C08K2201/011

  Nanostructured additives · CPC title

• C08L25/14

  with unsaturated esters · CPC title

• C08K9/06

  with silicon-containing compounds · CPC title

• C08K2201/003

  Additives being defined by their diameter · CPC title