Surface modification method and surface-modified elastic body

Patent metadata

Field	Value
Publication number	US-9982105-B2
Application number	US-201515039716-A
Country	US
Kind code	B2
Filing date	Jul 17, 2015
Priority date	Sep 18, 2014
Publication date	May 29, 2018
Grant date	May 29, 2018

Abstract

Provided are methods for surface-modifying a rubber vulcanizate or a thermoplastic elastomer, which can cost-effectively provide a variety of functions, e.g. sliding properties or liquid leakage resistance. Included is a method for surface-modifying a rubber vulcanizate or a thermoplastic elastomer as a modification target, the method including: step 1 of forming polymerization initiation points A on a surface of the modification target; step 2 of radically polymerizing a non-functional monomer starting from the points A to grow non-functional polymer chains; and step 3 of forming polymerization initiation points B on a surface of the non-functional polymer chains, radically polymerizing a polymerizable silane compound starting from the points B, and further reacting a perfluoroether group-containing silane compound to grow functional polymer chains, or step 3 ′ of adding a silane compound to a surface of the non-functional polymer chains and further reacting a perfluoroether group-containing silane compound to grow functional polymer chains.

First claim

The invention claimed is:

1. A method for surface-modifying a rubber vulcanizate or a thermoplastic elastomer as a modification target, the method comprising:
step 1 of forming polymerization initiation points A on a surface of the modification target;
step 2 of radically polymerizing a monomer A starting from the polymerization initiation points A to grow polymer chains A; and
step 3 of forming polymerization initiation points B on a surface of the polymer chains A, radically polymerizing a polymerizable silane compound starting from the polymerization initiation points B, and further reacting a perfluoroether group-containing silane compound to grow functional polymer chains, or step 3 ′ of adding a silane compound to a surface of the polymer chains A and further reacting a perfluoroether group-containing silane compound to grow functional polymer chains,
wherein the monomer A is at least one selected from the group consisting of acrylic acid, acrylic acid esters, alkali metal salts of acrylic acid, amine salts of acrylic acid, acrylamide, dimethylacrylamide, diethylacrylamide, isopropylacrylamide, hydroxyethylacrylamide, acryloylmorpholine, methoxymethyl acrylate, hydroxyethyl acrylate, methacrylic acid, methacrylic acid esters, alkali metal salts of methacrylic acid, amine salts of methacrylic acid, methacrylamide, dimethylmethacrylamide, diethylmethacrylamide, isopropylmethacrylamide, hydroxyethylmethacrylamide, methacryloylmorpholine, methoxymethyl methacrylate, hydroxyethyl methacrylate, and acrylonitrile.

2. The method according to claim 1 , wherein
the step 2 comprises radically polymerizing monomer A starting from the polymerization initiation points A by irradiation with LED light having a wavelength of 300 to 400 nm to grow polymer chains A, and
the step 3 comprises radically polymerizing a polymerizable silane compound starting from the polymerization initiation points B by irradiation with LED light having a wavelength of 300 to 400 nm and reacting a perfluoroether group-containing silane compound to grow functional polymer chains.

3. The method according to claim 1 , wherein
the step 1 comprises adsorbing a photopolymerization initiator A onto a surface of the modification target, optionally followed by irradiation with LED light having a wavelength of 300 to 400 nm, to form polymerization initiation points A from the photopolymerization initiator A on the surface, and
the step 3 comprises adsorbing a photopolymerization initiator B onto a surface of the polymer chains A, optionally followed by irradiation with LED light having a wavelength of 300 to 400 nm, to form polymerization initiation points B from the photopolymerization initiator B on the surface.

4. A method for surface-modifying a rubber vulcanizate or a thermoplastic elastomer as a modification target, the method comprising:
step I of radically polymerizing a monomer A in the presence of a photopolymerization initiator A on a surface of the modification target to grow polymer chains A; and
step II of radically polymerizing a polymerizable silane compound in the presence of a photopolymerization initiator B on a surface of the polymer chains A or adding a silane compound to a surface of the polymer chains A, and further reacting a perfluoroether group-containing silane compound to grow functional polymer chains,
wherein the monomer A is at least one selected from the group consisting of acrylic acid, acrylic acid esters, alkali metal salts of acrylic acid, amine salts of acrylic acid, acrylamide, dimethylacrylamide, diethylacrylamide, isopropylacrylamide, hydroxyethylacrylamide, acryloylmorpholine, methoxymethyl acrylate, hydroxyethyl acrylate, methacrylic acid, methacrylic acid esters, alkali metal salts of methacrylic acid, amine salts of methacrylic acid, methacrylamide, dimethylmethacrylamide, diethylmethacrylamide, isopropylmethacrylamide, hydroxyethylmethacrylamide, methacryloylmorpholine, methoxymethyl methacrylate, hydroxyethyl methacrylate, and acrylonitrile.

5. The method according to claim 3 , wherein the photopolymerization initiators A and B are the same as or different from each other and are each at least one of a benzophenone compound or a thioxanthone compound.

6. The method according to claim 1 , wherein the rubber vulcanizate or thermoplastic elastomer contains an allylic carbon atom which is adjacent to a double bond.

7. The method according to claim 1 , wherein the polymerization is carried out in an inert gas atmosphere.

8. The method according to claim 1 , wherein the polymerization is carried out under evacuation.

9. The method according to claim 1 , wherein the polymerizable silane compound is at least one selected from the group consisting of vinylalkoxysilanes, methacryloxyalkylalkoxysilanes, and acryloxyalkylalkoxysilanes.

10. The method according to claim 1 , wherein the silane compound is at least one of an alkoxysilane or a modified alkoxysilane.

11. The method according to claim 10 , wherein
the alkoxysilane and modified alkoxysilane each contain at least one selected from the group consisting of a methoxy group, an ethoxy group, a propoxy group, and a butoxy group, and
the modified alkoxysilane contains at least one selected from the group consisting of an amino group, a carboxyl group, a hydroxyl group, and a carboxy group.

12. The method according to claim 1 , wherein the perfluoroether group-containing silane compound is represented by the following formula (2) or (3):

wherein Rf 1 is a perfluoroalkyl group; Z is fluorine or a trifluoromethyl group; a, b, c, d, and e are the same as or different from one another and are each an integer of 0 or 1 or more, provided that a+b+c+d+e is 1 or more and the order of the repeating units parenthesized by subscripts a, b, c, d, and e occurring in the formula is not limited to that shown; Y is hydrogen or a C1-C4 alkyl group; X 1 is hydrogen, bromine, or iodine; R 1 is a hydroxyl group or a hydrolyzable substituent; R 2 is hydrogen or a monovalent hydrocarbon group; 1 is 0, 1, or 2; m is 1, 2, or 3; and n is an integer of 1 or more, provided that the two ends marked by * are directly bonded to each other, or

wherein Rf 2 is a divalent group that contains a unit represented by —(C k F 2k )O— where k is an integer of 1 to 6, and has a non-branched linear perfluoropolyalkylene ether structure; each R 3 is the same as or different from each other and represents a C1-C8 monovalent hydrocarbon group; each X 2 is the same as or different from each other and represents a hydrolyzable group or a halogen atom; each s is the same as or different from each other and represents an integer of 0 to 2; each t is the same as or different from each other and represents an integer of 1 to 5; and h and i are the same as or different from each other and each represent 1, 2, or 3.

13. The method according to claim 1 , wherein the entire polymer chain has a length of 500 to 50,000 nm.

14. A surface-modified elastic body, which is obtained by the method according to claim 1 .

15. A surface-modified elastic body, which is obtained by the method according to claim 1 , the elastic body being required to have sliding properties, low friction, or low water resistance in the presence of water or in a dry state.

16. A surface-modified elastic body, comprising a three-dimensional solid body at least part of whose surface is modified by the

Assignees

• Sumitomo Rubber Ind

Inventors

• Minagawa Yasuhisa

Classifications

• C08J2483/04

  Polysiloxanes · CPC title

• C08J2433/26

  Homopolymers or copolymers of acrylamide or methacrylamide · CPC title

• C08J2433/08

  Homopolymers or copolymers of acrylic acid esters · CPC title

• C08J2309/00

  Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons · CPC title

• C08J7/18 Primary

  using wave energy or particle radiation · CPC title