Water/oil repellent article, method for its production and water/oil repellent composition

Patent metadata

Field	Value
Publication number	US-11504740-B2
Application number	US-201916431202-A
Country	US
Kind code	B2
Filing date	Jun 4, 2019
Priority date	Mar 7, 2017
Publication date	Nov 22, 2022
Grant date	Nov 22, 2022

Abstract

To provide a water/oil repellent article which presents little burden on the environment, while being excellent in water/oil repellency, washing durability of the water repellency and friction durability of the water repellency; a method for producing such a water/oil repellent article; and a water/oil repellent composition and a water/oil repellent kit to be used for producing such a water/oil repellent article. A water/oil repellent article that comprises a substrate and, as adhered to the surface of the substrate, a fluorinated polymer having structural units based on monomer (a) having a C1-6 perfluoroalkyl group, and a specific fluorinated ether compound; a method for producing the water/oil repellent article, which comprises letting the fluorinated polymer and fluorinated ether compound be adhered to the substrate; a water/oil repellent composition which comprises the fluorinated polymer and fluorinated ether compound; and a water/oil repellent kit which comprises a first container accommodating a first liquid containing the fluorinated polymer and a second container accommodating a second liquid containing the fluorinated ether compound.

First claim

What is claimed is:

1. A method for producing a water/oil repellent article, comprising:
treating a substrate with a first liquid containing a fluorinated polymer having a structrual unit based on a monomer (a) having a C 1-6 perfluoroalkyl group; and
treating the substrate treated with the first liquid with a second liquid containing a fluorinated ether compound represented by formula (5):
A-U—W—V—B   (5),

where A and B are each independently —CF 3 , —OH, —C(O)OCH 3 , —C(O)OH or a hydrolyzable silyl group, excluding a case where both A and B are —C(O)OH; U is a divalent organic group which optionally has fluorine atom(s), an oxygen atom provided only when A is CF 3— , or a single bond; V is a divalent organic group which optionally has fluorine atom(s), or a single bond provided only when B is —CF 3 ; and W is a group represented by formula (6):
—(CF 2 CF 2 O) b (CF 2 O) c (CF 2 CF(CF 3 )O) d (CF(CF 3 )CF 2 O) c

(CF 2 CF 2 CF 2 O) f (CF 2 CF 2 CF 2 CF 2 O) g—   (6),

where b, c, d, e, f and g are each independently an integer of from 0 to 180, b+c+d+e+f+g is an integer of from 5 to 400, and the order of the respective oxyperfluoroalkylene units is not limited.

2. The method according to claim 1 , wherein the monomer (a) is a compound represented by formula (1):
(Z—Y) n X  (1),

where Z is a C 1-6 perfluoroalkyl group or a group represented by formula (2), Y is a divalent organic group having no fluorine atom, or a single bond, n is 1 or 2, and X is, when n is 1, any one of groups represented by formulae (3-1) to (3-5), and when n is 2, any one of groups represented by formulae (4-1) to (4-4):
C i F 2i+1 (CH 2 CF 2 ) p (CF 2 CF 2 ) q —  (2)

where i is an integer of from 1 to 6, p is an integer of from 1 to 4, and q is an integer of from 1 to 3,
—CR═CH 2   (3-1),

—C(O)OCR═CH 2   (3-2),

—OC(O)CR═CH 2   (3-3),

—OCH 2 -φ—CR═CH 2   (3-4),

—OCH═CH 2   (3-5),

where R is a hydrogen atom, a methyl group or a halogen atom, and φ is a phenylene group,
—CH[—(CH 2 ) m CR═CH 2 ]—  (4-1),

—CH[—(CH 2 ) m C(O)OCR═CH 2 ]—  (4-2),

—CH[—(CH 2 ) m OC(O)CR═CH 2 ]—  (4-3),

—OC(O)CH═CHC(O)O—  (4-4)

where R is a hydrogen atom, a methyl group or a halogen atom, and m is an integer of from 0 to 4.

3. The method according to claim 1 , wherein the fluorinated polymer further has a structural unit based on a monomer (b1), a structural unit based on a monomer (b2), or both:
wherein the monomer (b1) is a (meth)acrylate having no polyfluoroalkyl group and having a C 12-30 alkyl group, and
the monomer (b2) is a halogenated olefin.

4. The method according to claim 3 , wherein the fluorinated polymer further has a structural unit based on a monomer (c) having a cross-linkable functional group, and/or a structural unit based on a monomer (d) which is other than the monomers (a), (b1) and (b2).

5. The method according to claim 1 , wherein the second liquid further contains a fluorinated solvent having a boiling point at atmospheric pressure (normal boiling point) of at least 50° C.

6. The method according to claim 5 , wherein the fluorinated solvent is at least one member selected from the group consisting of 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-octane, 1,1,2,2-tetrafluoro-ethyl-2,2,2-trifluoroethyl ether, 1-methoxy-1,1,2,2,3,3,3-heptafluoropropane, 1-methoxy-1,1,2,2,3,3,4,4,4-nonafluorobutane, 1-ethoxy-1,1,2,2,3,3,4,4,4-nonafluorobutane, 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-trifluoromethyl-pentane, 1,1,1,2,2,3,4,5,5,5-decafluoropentane, poly(1,1,2,3,3,3-hexafluoropropene oxide), 1,3-bistrifluoromethylbenzene, 1,4-trifluoromethylbenzene, trifluorotoluene, perfluorobenzene and perfluorobutylamine.

7. The method according to claim 1 , wherein the amount of the fluorinated ether compound in the second liquid is from 0.1 to 100 parts by mass based on 100 parts by mass of the fluprinated polymer in the first liquid.

8. The method according to claim 1 , wherein the amount of the fluorinated ether compound in the second liquid is from 30 to 100 parts by mass based on 100 parts by mass of the fluorinated polymer in the first liquid.

9. The method according to claim 2 , wherein structural units of the fluorinated polymer consist of:
the structural unit based on the monomer (a); and
optionally at least one structural unit selected from the group consisting of
a structural unit based on a monomer (b1), where the monomer (b1) is a (meth)acrylate having no polyfluoroalkyl group and having a C 12-30 alkyl group,
a structural unit based on a monomer (b2), where the monomer (b2) is a halogenated olefin,
a structural unit based on a monomer (c), where the monomer (c) is N-methylol (meth)acrylamide, 2-hydroxyethyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, a 3,5-dimethylpyrazole adduct of 2-isocyanatoethyl (meth)acrylate, a 3,5-dimethylpyrazole adduct of 3-isocyanatopropyl (meth)acrylate, or 3-chloro-2-hydroxypropyl (meth)acrylate, and
a structural unit based on a monomer (d), where the monomer (d) is a maleic acid alkyl ester.

10. The method according to claim 9 ,
wherein the monomer (a) is F(CF 2 ) 6 CH 2 CH 2 OC(O)C(CH 3 )═CH 2 ,
the monomer (b1) is behenyl acrylate, stearyl acrylate, or behenyl methacrylate,
the monomer (b2) is vinylidene chloride or vinyl chloride,
the monomer (c) is 2-hydroxyethyl methacrylate or a 3,5-dimethylpyrazole adduct of 2-isocyanatoethyl methacrylate, and
the monomer (d) is maleic acid bis(2-ethylhexyl).

Assignees

• Agc Inc

Inventors

• SHIOTA Yukiko
• Hara Hiroyuki
• Isobe Akira
• Fukuda Reika

Classifications

• C09D123/28

  by reaction with halogens or compounds containing halogen (C09D123/32 takes precedence) · CPC title

• D06M15/53

  Polyethers (polyacetals D06M15/39) · CPC title

• B05D5/083 Primary

  involving the use of fluoropolymers · CPC title

• D06M15/256

  containing fluorine · CPC title

• C08L71/00

  Compositions of polyethers obtained by reactions forming an ether link in the main chain (of polyacetals C08L59/00; of epoxy resins C08L63/00; of polythioether-ethers C08L81/02; of polyether-sulfones C08L81/06); Compositions of derivatives of such polymers · CPC title