IP Library Granted Patent US 10,144,792
Granted Patent B2
US 10,144,792 · App. 15/226,356 · Granted Dec 4, 2018

Method for producing electric wire, method for producing molded artile, and method for producing resin material containing modified fluororesin

Inventors: Masatoshi Abe (Chiyoda-Ku, JP); Tomoya Hosoda (Chiyoda-ku, JP)
Assignee: AGC Inc.
C08F214/262C08F214/265C08J3/28C08J7/123H01B3/445C08J2327/18
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Quick Facts
Patent No.
US 10,144,792
App. No.
15/226,356
Granted
Dec 4, 2018
Kind
B2
Abstract

A method for producing an electric wire or a molded article with improved abrasion resistance is described. The method uses a fluororesin via electron beam irradiation in air at a temperature where the fluororesin does not melt. A method for producing a resin material containing a modified fluororesin is also described.

Claims (53)

1. A method for producing an electric wire comprising a conductor and an insulating layer containing a fluororesin and covering a surface of the conductor, the method comprising:

irradiating an electron beam to the insulating layer to modify at least part of the fluororesin, thereby forming an insulating layer containing a modified fluororesin,

wherein

the fluororesin

has a crystalline melting point prior to the electron beam irradiation Ta of at least 260° C.,

contains either one or both of a structural unit (a) having a carbonyl group-containing group and a main chain terminal group (a′) having a carbonyl group-containing group, and a structural unit (b) based on a perfluoromonomer which does not contain the structural unit (a), and

does not contain a structural unit based on a hydrocarbon monomer except for the structural unit (a); and

said irradiating is conducted at an irradiation dose of less than 30 kGy at a temperature of less than Ta in air.

2. The method according to claim 1 , wherein

the fluororesin is a copolymer comprising a structural unit (a1) based on a hydrocarbon monomer having either one or both of a carboxyl group and an acid anhydride group, a structural unit (b1) based on tetrafluoroethylene, and a structural unit (b2) based on a perfluoromonomer which is not tetrafluoroethylene, and

based on a total molar amount of the structural unit (a1), the structural unit (b1) and the structural unit (b2), the structural unit (a1) is from 0.01 to 5 mol %, the structural unit (b1) is from 50 to 99.89 mol %, and the structural unit (b2) is from 0.1 to 49.99 mol %.

3. A method for producing a molded article, the method comprising:

irradiating an electron beam to a molded article containing a fluororesin, to modify at least part of the fluororesin, thereby obtaining a molded article containing a modified fluororesin,

wherein

the fluororesin

has a crystalline melting point prior to the electron beam irradiation Ta of at least 260° C.,

contains either one or both of a structural unit (a) having a carbonyl group-containing group and a main chain terminal group (a′) having a carbonyl group-containing group, and a structural unit (b) based on a perfluorotnonomer which does not contain the structural unit (a), and

does not contain a structural unit based on a hydrocarbon monomer except for the structural unit (a); and

said irradiating is conducted at an irradiation dose of less than 30 kGy at a temperature of less than Ta in air.

4. The method according to claim 3 , wherein

the fluororesin is a copolymer comprising a structural unit (a1) based on a hydrocarbon monomer having either one or both of a carboxyl group and an acid anhydride group, a structural unit (b1) based on tetrafluoroethylene, and a structural (b2) based on a perfluoromonomer which is not tetrafluoroethylene, and

based on a total molar amount of the structural unit (a1), the structural unit (b1) and the structural unit (b2), the structural unit (a1) is from 0.01 to 5 mol %, the structural unit (b1) is from 50 to 99.89 mol %, and the structural unit (b2) is from 0.1 to 49.99 mol %.

5. A method for producing a resin material containing a modified fluororesin, the method comprising:

irradiating an electron beam to a resin material containing a fluororesin, to modify at least part of the fluororesin, thereby obtaining the resin material containing the modified fluororesin,

wherein

the fluororesin

has a crystalline melting point prior to the electron beam irradiation Ta of at least 260° C.,

contains either one or both of a structural unit (a) having a carbonyl group-containing group and a main chain terminal group (a′) having a carbonyl group-containing group, and a structural unit (h) based on a perfluoromononier which does not contain the structural unit (a), and

does not contain a structural unit based on a hydrocarbon monomer except for the structural unit (a); and

said irradiating is conducted at an irradiation dose of less than 30 kGy at a temperature of less than Ta in air.

6. The method according to claim 5 , wherein

the fluororesin is a copolymer comprising a structural unit (a1) based on a hydrocarbon monomer having either one or both of a carboxyl group and an acid anhydride group, a structural unit (b1) based on tetrafluoroethylene, and a structural unit (b2) based on a perfluoromonomer which is not tetrafluoroethylene, and

based on a total molar amount of the structural unit (a1), the structural unit (b1) and the structural unit (b2), the structural unit (a1) is from 0.01 to 5 mol %, the structural unit (b1) is from 50 to 99.89 mol %, and the structural unit (b2) is from 0.1 to 49.99 mol %.

7. A process for producing a molded article, the method comprising:

molding a resin material containing a modified fluororesin obtained by the method according to claim 6 , thereby obtaining the molded article.

8. The method according to claim 1 , wherein said irradiating satisfies 0.5≤Mb/Ma<1.2, where Ma represents a melt flow rate by g10 min of the fluororesin prior to the electron beam irradiation, and Mb represents a melt flow rate by g/10 min of the modified fluororesin after the electron beam irradiation.

9. The method according to claim 1 , wherein said irradiating satisfies 1≤Tb−Ta<6.5, where Tb is a crystalline melting point by ° C. of the modified fluororesin after the electron beam irradiation.

10. The method according to claim 1 , wherein said irradiating satisfies

0.5≤Mb/Ma<1.2, where Ma represents a melt flow rate by g/10 min of the fluororesin prior to the electron beam irradiation, and Mb represents a melt flow rate by g/10 min of the modified fluororesin after the electron beam irradiation; and

1≤Tb−Ta<6.5, where Tb is a crystalline melting point by ° C. of the modified fluororesin after the electron beam irradiation.

11. The method according to claim 1 , wherein said irradiating is conducted at a temperature of at most (Ta−5)° C.

12. The method according to claim 3 , wherein said irradiating satisfies 0.5≤Mb/Ma<1.2, where Ma represents a melt flow rate by g/10 min of the fluororesin prior to the electron beam irradiation, and Mb represents a melt flow rate by g/10 min of the modified fluororesin after the electron beam irradiation.

13. The method according to claim 3 , wherein said irradiating satisfies 1≤Tb−Ta<6.5 where Tb is a crystalline melting point by ° C. of the modified fluororesin after the electron beam irradiation.

14. The method according to claim 3 , wherein said irradiating satisfies

0. 5≤Mb/Ma<1.2, where Ma represents a melt flow rate by g/10 min of the fluororesin prior to the electron beam irradiation, and Mb represents a melt flow rate by g/10 min of the modified fluororesin after the electron beam irradiation; and

1≤Tb−Ta<6.5, where Tb is a crystalline melting point by ° C. of the modified fluororesin after the electron beam irradiation.

15. The method according to claim 3 , wherein said irradiating is conducted at a temperature of at most (Ta−5)° C.

16. The method according to claim 5 , wherein said irradiating satisfies 0.5≤Mb/Ma<1.2, where Ma represents a melt flow rate by g/10 min of the fluororesin prior to the electron beam irradiation, and Mb represents a melt flow rate by g/10 min of the modified fluororesin after the electron beam irradiation.

17. The method according to claim 5 , wherein said irradiating satisfies 1≤Tb−Ta<6.5, where Tb is a crystalline melting point by ° C. of the modified fluororesin after the electron beam irradiation.

18. The method according to claim 5 , wherein said irradiating satisfies

0. 5≤Mb/Ma<1.2, where Ma represents a melt flow rate by g/10 min of the fluororesin prior to the electron beam irradiation, and Mb represents a melt flow rate by g/10 min of the modified fluororesin after the electron beam irradiation; and

1≤Tb−Ta<6.5, where Tb is a crystalline melting point by ° C. of the modified fluororesin after the electron beam irradiation.

19. The method according to claim 5 , wherein said irradiating is conducted at a temperature of at most (Ta−5)° C.

Assignments (2)
CHANGE OF NAME Recorded Aug 7, 2018
From: ASAHI GLASS COMPANY, LIMITED
To: AGC INC.
Reel/Frame 046730/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2016
From: ABE, MASATOSHI; HOSODA, TOMOYA
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 039317/0707 →
Priority Claims (1)
JP 2014-035140 · Feb 26, 2014 · national
Continuity (2)
Continuation PCTJP2015055447 · Feb 25, 2015
Related Publication 20160340455A1 · Nov 24, 2016