Surface modification method and surface-modified elastic body

Patent metadata

Field	Value
Publication number	US-10344109-B2
Application number	US-201314421319-A
Country	US
Kind code	B2
Filing date	Sep 9, 2013
Priority date	Sep 10, 2012
Publication date	Jul 9, 2019
Grant date	Jul 9, 2019

Abstract

The present invention aims to provide methods for surface-modifying a rubber vulcanizate or a thermoplastic elastomer, which can cost-effectively impart a variety of functions, such as sliding properties or biocompatibility, according to the application. The present invention relates to a method for surface-modifying an object of a rubber vulcanizate or a thermoplastic elastomer, the method including: step 1 of forming polymerization initiation points A on the surface of the object; and step 2 of radically polymerizing a non-functional monomer, starting from the polymerization initiation points A, to grow non-functional polymer chains, and further radically polymerizing a fluorine-containing functional monomer to grow fluorine-containing functional polymer chains.

First claim

The invention claimed is:

1. A method for surface-modifying an object of a rubber vulcanizate or a thermoplastic elastomer, the method comprising:
step 1 of forming polymerization initiation points A on a surface of the object; and
step 2 of radically polymerizing a non-functional monomer, starting from the polymerization initiation points A, to grow non-functional polymer chains, and further radically polymerizing a fluorine-containing functional monomer to grow fluorine-containing functional polymer chains on the non-functional polymer chains,

wherein
the non-functional monomer is at least one selected from the group consisting of acrylic acid, acrylic acid esters, acrylic acid alkali metal salts, acrylic acid amine salts, acrylamide, dimethylacrylamide, diethylacrylamide, isopropylacrylamide, hydroxyethylacrylamide, acryloylmorpholine, methoxymethyl acrylate, hydroxyethyl acrylate, methacrylic acid, methacrylic acid esters, methacrylic acid alkali metal salts, methacrylic acid amine salts, methacrylamide, dimethylmethacrylamide, diethylmethacrylamide, isopropylmethacrylamide, hydroxyethylmethacrylamide, methacryloylmorpholine, methoxymethyl methacrylate, hydroxyethyl methacrylate, and acrylonitrile; and
the fluorine-containing functional monomer is a fluorine-containing (meth)acrylic-modified organic silicon compound that is obtained by an addition reaction of an unsaturated monocarboxylic acid (B) containing a (meth)acrylic group with a fluorine-containing epoxy-modified organic silicon compound (A) represented by the following formula (1):

wherein
Rf 11 represents a monovalent or divalent group having a molecular weight of 100 to 40,000 and containing a fluoroalkyl structure or a fluoropolyether structure;
Q 11 represents a linking group which comprises a siloxane structure, an unsubstituted or halogen-substituted silalkylene structure, a silarylene structure, or a combination of two or more thereof, each of which contains at least (a+b) silicon atoms and has a valency of (a+b), and Q 11 may have a cyclic structure;
Q 12 represents a C1-20 divalent hydrocarbon group and Q 12 may have a cyclic structure and may be interrupted by an ether linkage or an ester linkage;
R 11 to R 13 each independently represent a hydrogen atom or a C1-10 monovalent hydrocarbon group, provided that a part or all of the hydrogen atoms of R 11 to R 13 may be replaced with a halogen atom, and R 11 and R 12 may be joined to each other to form a ring together with the carbon atoms to which they are attached;
when Rf 11 is a monovalent group, a′ and a represent 1 and an integer of 1 to 6, respectively, and when Rf 11 is a divalent group, a and a′ represent 1 and 2, respectively; and b represents an integer of 1 to 20.

2. The method according to claim 1 , wherein the step 1 comprises adsorbing a photopolymerization initiator onto the surface of the object, optionally followed by irradiation with LED light having a wavelength of 300 to 400 nm, to form polymerization initiation points from the photopolymerization initiator on the surface.

3. The method according to claim 1 , wherein the step 2 comprises radically polymerizing a non-functional monomer, starting from the polymerization initiation points A, by irradiation with LED light having a wavelength of 300 to 450 nm to grow non-functional polymer chains, and further radically polymerizing a fluorine-containing functional monomer by irradiation with LED light having a wavelength of 300 to 450 nm to grow fluorine-containing functional polymer chains.

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

5. The method according to claim 2 , wherein the photopolymerization initiator is at least one of a benzophenone compound and a thioxanthone compound.

6. The method according to claim 3 , wherein the method comprises inserting an inert gas into a reaction container and a reaction solution during or before the light irradiation, and polymerizing the monomer in an atmosphere replaced with the inert gas.

7. The method according to claim 1 , wherein, in the formula (1), Rf 11 contains 1 to 500 repeating units of the following formula:
—C i F 2i O—

wherein i in each unit independently represents an integer of 1 to 6.

8. The method according to claim 1 ,
wherein, in the formula (1), Q 11 is represented by the following formula (2):

wherein a and b are as defined in the formula (1); the broken lines represent bonds; the unit comprising a repeating unit repeated a times is joined to Rf 11 ; the unit comprising a repeating unit repeated b times is joined to a group represented by the following formula:

wherein Q 12 and R 11 to R 13 are as defined in the formula (1); the two types of repeating units are randomly arranged; and Rf 11 is as defined in the formula (1).

9. The method according to claim 1 ,
wherein, in the formula (1), Rf 11 is represented by the following formula (3):

wherein Rf′ 11 represents a divalent perfluoropolyether group having a molecular weight of 300 to 30,000 which may be internally branched; Q 13 represents a divalent organic group which may contain an oxygen atom, a nitrogen atom, a fluorine atom or a silicon atom and may have a cyclic structure or an unsaturated bond; Q f 11 represents Q 13 or a fluorine atom; T represents a linking group represented by the following formula (4):

wherein R 11 to R 13 , Q 12 , a, and b are as defined in the formula (1), and Q 14 represents a linking group which comprises a siloxane structure, an unsubstituted or halogen-substituted silalkylene structure, a silarylene structure, or a combination of two or more thereof, each of which contains at least (a+b) silicon atoms and has a valency of (a+b); and v represents an integer of 0 to 5, provided that v is 0 when Q f 11 is a fluorine atom.

10. The method according to claim 1 ,
wherein the fluorine-containing functional monomer is a mixture of a fluorine-containing epoxy-modified organic silicon compound represented by the formula below and a fluorine-containing (meth)acrylic-modified organic silicon compound represented by the formula below:

wherein b′ 1 +b′ 2 is 2 to 6.5, and Rf′ 12 is a group represented by the following formula:

wherein n 1 is 2 to 100.

11. The method according to claim 1 , wherein the fluorine-containing functional monomer has an infrared absorption spectrum comprising strong absorption peaks at about 1045 cm −1 and about 1180 cm −1 , absorption peaks at about 806 cm −1 and about 1720 cm −1 , a weak absorption peak at about 1532 cm −1 , and a broad weak absorption peak at about 3350 cm −1 .

12. The method according to claim 1 , wherein the fluorine-containing functional monomer has a 13 C NMR spectrum in chloroform-d solution comprising signals at chemical shifts of about 13.01, 14.63, 23.04, 40.

Assignees

• Sumitomo Rubber Ind

Inventors

• Minagawa Yasuhisa

Classifications

• C08J2323/22

  Copolymers of isobutene; butyl rubber · CPC title

• C08J2319/00

  Characterised by the use of rubbers not provided for in groups C08J2307/00 - C08J2317/00 · CPC title

• C08J7/18

  using wave energy or particle radiation · CPC title

• C08F2/50 Primary

  with sensitising agents · CPC title

• B60C13/04

  having annular inlays or covers, e.g. white sidewalls · CPC title