Fluororesin, fluororesin particles, and methods for producing these

Patent metadata

Field	Value
Publication number	US-12528894-B2
Application number	US-202318471794-A
Country	US
Kind code	B2
Filing date	Sep 21, 2023
Priority date	Sep 28, 2018
Publication date	Jan 20, 2026
Grant date	Jan 20, 2026

Abstract

The present invention relates to resin particles including a residue unit represented by the following general formula (1) and having a volume average particle diameter equal to or more than 5 μm and equal to or less than 2008 μm, and a method for producing thereof. Fruthermore the present invention relates to a fluororesin comprising a residue unit represented by a general formula (1) and having a weight average molecular weight Mw in a range of 5×10 4 to 3×10 5 , and a yellow index of a heat-melted molded product (thickness 3 mm) after 24 h at 280° C. of equal to or less than 6, and a method for producing thereof.

In the formula (1), Rf 1 , Rf 2 , Rf 3 , and Rf 4 are each independently one of the groups consisting of a fluorine atom, a linear perfluoroalkyl group having 1 to 7 carbon atoms, a branched perfluoroalkyl group having 3 to 7 carbon atoms, or a cyclic perfluoroalkyl group having 3 to 7 carbon atoms. The perfluoroalkyl group may have an ethereal oxygen atom. Further, Rf 1 , Rf 2 , Rf 3 , and Rf 4 may be linked to one another to form a ring having 4 or more and 8 or less carbon atoms, and the ring may include an ethereal oxygen atom.

First claim

The invention claimed is:

1 . A fluororesin, comprising:
a resin comprising a residue unit of the following formula (1) and having a weight average molecular weight Mw of from 5×10 4 to 3×10 5 , wherein a molded product made from the resin heat-melted for 24 h at 280° C. and formed in a thickness of 3 mm has a yellow index of 6 or less,

wherein Rf 1 , Rf 2 , Rf 3 , and Rf 4 are each independently selected from the group consisting of a fluorine atom, a linear perfluoroalkyl group having 1 to 7 carbon atoms, a branched perfluoroalkyl group having 3 to 7 carbon atoms, and a cyclic perfluoroalkyl group having 3 to 7 carbon atoms, the linear or branched perfluoroalkyl group optionally have an ethereal oxygen atom, Rf 1 , Rf 2 , Rf 3 , and Rf 4 may be linked to one another to form a ring having 4 to 8 carbon atoms, and the ring optionally includes an ethereal oxygen atom,
which the fluororesin has a molecular weight distribution Mw/Mn of from 1.2 to 8.

2 . The fluororesin according to claim 1 , wherein a glass transition temperature of the fluororesin is from 125° C. to 145° C.

3 . The fluororesin according to claim 1 , wherein a melt viscosity of the fluororesin at a shear rate of 10 −2 s and 250° C. is from 1×10 2 to 3×10 5 Pa·s.

4 . The fluororesin according to claim 1 , wherein a molded product made from the resin heat-melted for 24 h at 280° C. and formed in a thickness of 3 mm and a diameter of 26.4 mm has 10 or less cracks.

5 . The fluororesin according to claim 1 , wherein the resin satisfies a difference B−A of 1.0% or less, where A is an amount of weight loss immediately after a temperature is raised to 300° C. at 10° C./min in air in TG-DTA, and B is an amount of weight loss after the temperature is raised to 300° C. and then held at 300° C. for 30 min.

6 . The fluororesin according to claim 1 , wherein a molded product made from the resin heat-melted for 24 h at 280° C. and formed in a thickness of 3 mm and a diameter of 26.4 mm has an area occupied by bubbles of 10% or less relative to an area of the molded product.

7 . The fluororesin according to claim 1 , wherein a molded product made from the resin heat-melted for 24 h at 280° C. and formed in a thickness of 3 mm and a diameter of 26.4 mm has 10 or less bubbles.

8 . The fluororesin according to claim 1 , wherein the weight average molecular weight Mw of the fluororesin is from 5×10 4 to 2×10 5 .

9 . The fluororesin according to claim 1 , wherein a molded product made from the resin heat-melted for 24 h at 280° C. and formed in a thickness of 3 mm has a yellow index of 4 or less.

10 . The fluororesin according to claim 1 , Wherein a melt viscosity of the of the fluororesin at a shear rate of 10 −2 s and 250° C. is from 1×10 2 to 5×10 4 Pa·s.

11 . The fluororesin according to claim 1 , wherein the resin comprises a residue unit of the following formula (2):

12 . A method for producing a fluororesin, comprising:
polymerizing a monomer of the following formula (3) in a presence of a radical polymerization initiator and a chain transfer agent, thereby obtaining a fluororesin that comprises a residue unit of the following formula (4), wherein the chain transfer agent comprises an organic compound having 1 to 20 carbon atoms and including at least one atom selected from the group consisting of a hydrogen atom and a chlorine atom, and the fluororesin has a weight average molecular weight Mw of from 5×10 4 to 3×10 5 and has a yellow index of 6 or less when formed into a molded product in a thickness of 3 mm after heat-melting for 24 h at 280° C.,

wherein Rf 5 , Rf 6 , Rf 7 , and Rf 8 are each independently selected from the group consisting of a fluorine atom, a linear perfluoroalkyl group having 1 to 7 carbon atoms, a branched perfluoroalkyl group having 3 to 7 carbon atoms, or a cyclic perfluoroalkyl group having 3 to 7 carbon atoms; the linear or branched perfluoroalkyl group optionally have an ethereal oxygen atom; Rf 5 , Rf 6 , Rf 7 , and Rf 8 may be linked to one another to form a ring having 4 to 8 carbon atoms; and the ring optionally includes an ethereal oxygen atom.

13 . The production method according to claim 12 , wherein an amount of the chain transfer agent is 3% by weight to 50% by weight based on a total amount of the monomer and the chain transfer agent.

14 . The production method according to claim 12 , wherein the polymerizing is carried out in an organic solvent that dissolves the monomer of the formula (3) and precipitates the fluororesin including the residue unit of the formula (4).

15 . The production method according to claim 12 , wherein the chain transfer agent comprises an organic compound having 1 to 20 carbon atoms and including a chlorine atom.

16 . The production method according to claim 12 , wherein the chain transfer agent comprises an organic compound having 1 to 20 carbon atoms and including a chlorine atom and a hydrogen atom.

Assignees

• Tosoh Corp
• Nitto Denko Corp

Inventors

• Yumino Shohei
• Shimono Tomoya
• Sakaguchi Kota
• NAGAI Tomonari
• Iwanaga Kazunari
• Tanabiki Masao
• Doi Toru

Classifications

• C08F116/38

  by a acetal or ketal radical · CPC title

• C08F16/38

  by an acetal or ketal radical · CPC title

• C08F2/38

  Polymerisation using regulators, e.g. chain terminating agents {, e.g. telomerisation} · CPC title

• C08F2/06

  Organic solvent · CPC title

• C08F24/00 Primary

  Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen (cyclic esters of polyfunctional acids C08F18/00; cyclic anhydrides of unsaturated acids C08F20/00, C08F22/00) · CPC title