JP2024064171A - Composition for crosslinking fluororubber and molded article - Google Patents

Abstract

To provide a composition for crosslinking a fluororubber capable of obtaining a molded article having high cross-linking density and excellent tensile strength.SOLUTION: There is provided a composition for crosslinking a fluororubber which comprises a fluororubber (a), a crosslinking agent (b), a dehydrofluorinating agent (c) and an organic peroxide (d), wherein the crosslinking agent (b) is a compound which has 1) at least one aromatic ring, 2) a group having a carbon-carbon double bond (except that constituting the aromatic ring) and 3) an alkylcarbonyloxy group bonded directly to a carbon atom constituting the aromatic ring in the molecule.SELECTED DRAWING: None

Description

This disclosure relates to a composition for crosslinking fluororubber and a molded article.

Patent document 1 describes a graftable fluoroelastomer composition that includes a polyhydroxy-curable fluoroelastomer that is substantially free of nucleophilic end groups; a monophenolic grafting agent; an accelerator; and an acid acceptor, and is characterized in that the composition has a Mooney viscosity of ML(1+18) of less than 160 at 135°C.

Patent Document 2 describes a curable partially fluorinated polymer composition that includes: (i) a partially fluorinated amorphous fluoropolymer that includes a carbon-carbon double bond or that can form a carbon-carbon double bond within the partially fluorinated amorphous fluoropolymer chain, the partially fluorinated amorphous fluoropolymer being substantially free of bromine, iodine, and nitrile; and (ii) a curing agent that includes a terminal olefin having at least one olefinic hydrogen.

JP 2008-502789 A JP 2017-538023 A

The objective of this disclosure is to provide a composition for cross-linking fluororubber that can produce molded products with high cross-link density and excellent tensile strength.

According to the present disclosure, there is provided a composition for crosslinking fluororubber, which contains a fluororubber (a), a crosslinking agent (b), a dehydrofluorination agent (c), and an organic peroxide (d), and the crosslinking agent (b) is a compound having within its molecule 1) at least one aromatic ring, 2) a group having a carbon-carbon double bond (excluding those constituting the aromatic ring), and 3) an alkylcarbonyloxy group directly bonded to a carbon atom constituting the aromatic ring.

According to the present disclosure, it is possible to provide a fluororubber cross-linking composition that can produce molded products with high cross-linking density and excellent tensile strength.

Specific embodiments of the present disclosure are described in detail below, but the present disclosure is not limited to the following embodiments.

The fluororubber cross-linking composition disclosed herein contains a fluororubber (a), a cross-linking agent (b), a dehydrofluorination agent (c), and an organic peroxide (d).

In US Pat. No. 5,399,633, the above-mentioned compositions are proposed as compositions for making grafted fluoroelastomers, such as eugenol-grafted fluoroelastomers. A monophenol grafting agent, such as eugenol (2-methoxy-4-allylphenol), is used not as a crosslinking agent, but to make grafted fluoroelastomers that are resistant to premature vulcanization.

However, there is no known technology that uses a compound that has a group with a carbon-carbon double bond in the molecule and also has an aromatic ring to which an alkylcarbonyloxy group is bonded as a crosslinking agent for fluororubber.

It has been discovered that by using a compound that has a group with a carbon-carbon double bond in the molecule and also has an aromatic ring to which an alkylcarbonyloxy group is bonded as a crosslinking agent for fluororubber, the crosslinking reaction of the fluororubber proceeds smoothly, the crosslink density of the resulting molded product is surprisingly high, and the mechanical properties of the molded product, such as the tensile strength, are also improved.

Below, we will explain each component of the disclosed fluororubber cross-linking composition.

(a) Fluororubber The fluororubber crosslinking composition of the present disclosure contains fluororubber. In the present disclosure, fluororubber is an amorphous fluoropolymer. "Amorphous" means that the magnitude of the melting peak (ΔH) that appears in differential scanning calorimetry [DSC] (heating rate 10°C/min) or differential thermal analysis [DTA] (heating rate 10°C/min) of the fluoropolymer is 4.5 J/g or less. Fluororubber exhibits elastomeric properties by crosslinking. Elastomeric properties refer to the property that the polymer can be stretched and can retain its original length when the force required to stretch the polymer is no longer applied.

The fluororubber may be a partially fluorinated rubber or a perfluororubber, but is preferably a partially fluorinated rubber. A partially fluorinated rubber is a fluoropolymer that contains fluoromonomer units and has a perfluoromonomer unit content of less than 90 mol% relative to the total polymerized units, has a glass transition temperature of 20°C or less, and has a melting peak (ΔH) of 4.5 J/g or less.

A perfluoromonomer is a monomer that does not contain a carbon atom-hydrogen atom bond in the molecule. The perfluoromonomer may be a monomer in which some of the fluorine atoms bonded to the carbon atom are replaced with chlorine atoms, in addition to carbon atoms and fluorine atoms, and may also have nitrogen atoms, oxygen atoms, sulfur atoms, phosphorus atoms, boron atoms, or silicon atoms in addition to carbon atoms. The perfluoromonomer is preferably a monomer in which all hydrogen atoms are replaced with fluorine atoms. The perfluoromonomer does not include monomers that provide crosslinking sites.

A monomer that provides a crosslinking site is a monomer (cure site monomer) that has a crosslinkable group that provides the fluoropolymer with a crosslinking site for forming a crosslink with a crosslinking agent.

The fluororubber used in the present disclosure is not particularly limited, and examples thereof include fluororubbers known as peroxide-crosslinkable fluororubbers and fluororubbers known as polyol-crosslinkable fluororubbers. In addition, the fluororubber may be a fluororubber that can be crosslinked using a pyridinium-type salt as described in JP-T-2018-514627.

The peroxide-crosslinkable fluororubber is a fluororubber having a peroxide-crosslinkable site. The peroxide-crosslinkable site is not particularly limited, and examples thereof include an iodine atom, a bromine atom, and a CN group that the fluororubber has; and a carbon-carbon unsaturated bond that exists in the main chain or side chain of the fluororubber. In the present disclosure, a peroxide-crosslinkable fluororubber may be used as the fluororubber, but this does not mean that the crosslinking reaction of the fluororubber crosslinking composition of the present disclosure proceeds in the same manner as the crosslinking reaction of a conventionally known peroxide-crosslinkable fluororubber.

The polyol-crosslinkable fluororubber is a fluororubber having a polyol-crosslinkable site. As the polyol-crosslinkable fluororubber, polyol-crosslinkable partially fluorinated rubber is preferable. As the polyol-crosslinkable fluororubber, there is no particular limitation, and examples thereof include vinylidene fluoride (VdF)-based fluororubber. In the present disclosure, a polyol-crosslinkable fluororubber may be used as the fluororubber, but this does not mean that the crosslinking reaction of the fluororubber crosslinking composition of the present disclosure proceeds in the same manner as the crosslinking reaction of a conventionally known polyol-crosslinkable fluororubber.

Examples of fluororubbers having a polyol-crosslinkable site include VdF-based fluororubbers, rubbers having polyol-crosslinkable functional sites in the side chain and/or main chain, etc. Examples of fluororubbers having a polyol-crosslinkable site include non-perfluoro fluororubbers, fluororubbers containing -CH ₂ - (methylene group) in the main chain, etc. Examples of fluororubbers having a polyol-crosslinkable site include, for example,
A vinylidene fluoride (VDF)-based fluoroelastomer having substantially no polar terminal group, as described in JP-A-2003-277563;
A vinylidene fluoride-based fluoroelastomer comprising a repeating unit derived from vinylidene fluoride (VDF) and a repeating unit derived from at least one additional (per)fluorinated monomer as described in JP-A-2018-527449;
It may be 100 parts (phr) of a cured fluoroelastomer having a small amount of fluorine of less than 67% by weight as described in JP-A-7-316377, containing 40 to 68% by weight of vinylidene fluoride (VDF) units and 20 to 50% by weight of hexafluoropropylene (HFP) units in total to 100, and optionally containing one or more comonomers having ethylene unsaturation.

The fluororubber used in this disclosure is preferably a fluororubber containing vinylidene fluoride (VdF) units (VdF-based fluororubber).

Examples of VdF-based fluororubbers include tetrafluoroethylene (TFE)/propylene/VdF-based fluororubbers, ethylene/hexafluoropropylene (HFP)/VdF-based fluororubbers, VdF/HFP-based fluororubbers, and VdF/TFE/HFP-based fluororubbers. These fluororubbers having polyol-crosslinkable sites can be used alone or in any combination within the scope that does not impair the effects of the present disclosure.

The VdF-based fluororubber is preferably one represented by the following general formula (1):

-(M ¹ )-(M ² )-(N ¹ )-(1)
(In the formula, the structural unit ^M1 is a structural unit derived from vinylidene fluoride ( ^m1 ), the structural unit ^M2 is a structural unit derived from a fluorine-containing ethylenic monomer ( ^m2 ), and the structural unit ^N1 is a repeating unit derived from the monomer ( ^m1 ) and a monomer ( ⁿ¹ ) copolymerizable with the monomer ( ^m2 ).)

Among the VdF-based fluororubbers represented by the general formula (1), those containing 30 to 85 mol % of the structural unit ^M1 and 55 to 15 mol % of the structural unit ^M2 are preferred, and more preferably 50 to 80 mol % of the structural unit ^M1 and 50 to 20 mol % of the structural unit ^M2 . The amount of the structural unit ^N1 is preferably 0 to 20 mol % based on the total amount of the structural units ^M1 and ^M2 .

As the fluorine-containing ethylenic monomer (m ² ), one or more monomers can be used, such as TFE, chlorotrifluoroethylene (CTFE), trifluoroethylene, HFP, trifluoropropylene, tetrafluoropropylene, pentafluoropropylene, trifluorobutene, tetrafluoroisobutene, perfluoro(alkyl vinyl ether) (PAVE), and monomers represented by the general formula (2):
_CF2 =CFO( ^Rf1O ) _q ( ^{Rf2O )} _rRf3 (2)
(wherein ^Rf1 and ^Rf2 each independently represent a linear or branched perfluoroalkylene group having 1 to 6 carbon atoms, ^{Rf3 each} independently represent a linear or branched perfluoroalkyl group having 1 to 6 carbon atoms, and q and r each independently represent an integer of 0 to 6 (with the proviso that 0<q+r≦6 is satisfied)), a fluorine-containing monomer represented by general formula (3):
^CHX11 = ^CX12Rf4 ( ³ )
(wherein one of ^X11 and ^X12 is H and the other is F, and ^Rf4 is a linear or branched fluoroalkyl group having 1 to 12 carbon atoms), and vinyl fluoride. Among these, TFE, HFP and PAVE are preferred.

The monomer (n ¹ ) may be any monomer that is copolymerizable with the monomer (m ¹ ) and the monomer (m ² ), and examples thereof include ethylene, propylene, alkyl vinyl ether, a monomer that provides a crosslinking site, a bisolefin compound, etc. These may be used alone or in any combination.

Examples of monomers that provide such crosslinking sites include those represented by the general formula (4):
CY ¹ ₂ ═CY ¹ −Rf ⁵ CHR ¹ X ⁴¹ (4)
(wherein Y ¹ is independently a hydrogen atom, a fluorine atom or -CH ₃ , Rf ⁵ is a fluoroalkylene group, a perfluoroalkylene group, a fluoropolyoxyalkylene group or a perfluoropolyoxyalkylene group, R ¹ is a hydrogen atom or -CH ₃ , and X ⁴¹ is an iodine atom or a bromine atom), an iodine- or bromine-containing monomer represented by the general formula (5):
_CF2 =CFO( _CF2CF ( _CF3 )O) _m ( _CF2 ) _n - ^X51 (5)
(wherein m is an integer of 0 to 5, n is an integer of 1 to 3, and ^X51 is a cyano group, a carboxyl group, an alkoxycarbonyl group, a bromine atom, or an iodine atom),
_CH2 =CH( _CF2 ) _pI (6)
(wherein p is an integer of 1 to 10), and the like. For example, iodine-containing monomers such as perfluoro(6,6-dihydro-6-iodo-3-oxa-1-hexene) and perfluoro(5-iodo-3-oxa-1-pentene) as described in JP-B-5-63482 and JP-A-7-316234, and CF ₂ ═CFOCF ₂ CF ₂ CH ₂ as described in JP-A-4-217936 are included. Examples of the monomers include iodine-containing monomers such as iodine-containing monomer I, iodine-containing monomers such as 4-iodo-3,3,4,4-tetrafluoro-1-butene described in JP-A-61-55138, bromine-containing monomers described in JP-A-4-505341, cyano group-containing monomers, carboxyl group-containing monomers, and alkoxycarbonyl group-containing monomers described in JP-A-4-505345 and JP-A-5-500070. These can be used alone or in any combination.
As the bisolefin compound, those described in JP-A-8-12726 can be used.

Specific examples of the VdF-based fluororubber include VdF/HFP-based rubber, VdF/HFP/TFE-based rubber, VdF/TFE/PAVE-based fluororubber, VdF/CTFE-based rubber, and VdF/CTFE/TFE-based rubber.

Examples of rubbers having polyol-crosslinkable functional sites in the side chain and/or main chain include rubbers constituted of copolymer units of cure site monomers represented by tetrafluoroethylene (TFE)/perfluoro(alkyl vinyl ether) (PAVE)/R ¹ CH═CR ² R ³ (wherein R ¹ and R ² are independently selected from hydrogen and fluorine, and R ³ is independently selected from hydrogen, fluorine, alkyl, and perfluoroalkyl) as described in JP-A-60-44511 or JP 3,890,630, and rubbers having double bonds in the side chain and/or main chain.

Among these, the fluororubber is preferably a fluororubber made of VdF and at least one other fluorine-containing monomer, and is particularly preferably at least one rubber selected from the group consisting of VdF/HFP-based fluororubber, VdF/TFE/HFP-based fluororubber, and VdF/TFE/PAVE-based fluororubber, and more preferably at least one rubber selected from the group consisting of VdF/HFP-based fluororubber and VdF/TFE/HFP-based fluororubber.

The fluororubber preferably has a Mooney viscosity at 100°C (ML1+10(100°C)) of 2 or more, more preferably 10 or more, even more preferably 20 or more, and particularly preferably 30 or more. It is also preferably 200 or less, more preferably 150 or less, even more preferably 120 or less, and particularly preferably 100 or less. The Mooney viscosity is measured in accordance with ASTM D1646-15 and JIS K6300-1:2013.

The fluorine content of the fluororubber is preferably 50 to 75% by mass. More preferably, it is 60 to 73% by mass, and even more preferably, it is 63 to 72% by mass. The fluorine content is calculated from the composition ratio of the monomer units that make up the fluororubber.

The fluororubber preferably has a glass transition temperature of -50 to 0°C. The glass transition temperature can be determined by obtaining a DSC curve using a differential scanning calorimeter by heating 10 mg of a sample at 20°C/min, and determining the glass transition temperature as the temperature at the intersection of an extension of the baseline before and after the secondary transition of the DSC curve and a tangent to the inflection point of the DSC curve.

The fluororubber may have at least one of iodine atoms and bromine atoms, or may have iodine atoms. The total content of iodine atoms and bromine atoms in the fluororubber is preferably 0.001 to 10 mass%, more preferably 5.0 mass% or less, even more preferably 1.0 mass% or less, particularly preferably 0.7 mass% or less, most preferably 0.5 mass% or less, more preferably 0.01 mass% or more, even more preferably 0.05 mass% or more, particularly preferably 0.08 mass% or more, and most preferably 0.10 mass% or more. The bonding positions of the iodine atoms and bromine atoms in the fluororubber may be the terminals of the main chain or the terminals of the side chain of the fluororubber, or of course both.

The _iodine content can be measured by the following method: _{Na2CO3 and K2CO3} are mixed in a 1:1 (weight ratio), and the resulting mixture is dissolved in 20 ml of pure water to prepare an absorption liquid, and 5 _mg of _Na2SO3 is mixed with 12 mg of a sample (fluoropolymer) to prepare a mixture, which is burned in oxygen in a quartz flask, and the generated combustion gas is introduced into the absorption liquid, and the resulting absorption liquid is left to stand for 30 minutes, after which the concentration of iodine ions in the absorption liquid is measured using a Shimadzu 20A ion chromatograph, and the iodine ion content can be determined from the measured value using a calibration curve prepared using a KI standard solution containing 0.5 ppm iodine ions and a KI standard solution containing 1.0 ppm iodine ions.

Fluororubber containing at least one of iodine and bromine atoms can be produced, for example, by a method of polymerizing iodine- or bromine-containing monomers, or by a method of polymerizing using a bromine compound or an iodine compound as a polymerization initiator or chain transfer agent.

Examples of the polymerization method using a bromine compound or an iodine compound as a chain transfer agent include a method in which emulsion polymerization is carried out in an aqueous medium under pressure in the presence of a bromine compound or an iodine compound in a substantially oxygen-free state (iodine transfer polymerization method).
General formula _: ^R8IxBr _y
(wherein x and y are each an integer of 0 to 2 and satisfy 1≦x+y≦2; and ^R8 is a saturated or unsaturated fluorohydrocarbon group or chlorofluorohydrocarbon group having 1 to 16 carbon atoms, or a hydrocarbon group having 1 to 3 carbon atoms, which may contain an oxygen atom).

Examples of the bromine compound and the iodine compound include 1,3-diiodoperfluoropropane, 2-iodoperfluoropropane, 1,3-diiodo-2-chloroperfluoropropane, 1,4-diiodoperfluorobutane, 1,5-diiodo-2,4-dichloroperfluoropentane, 1,6-diiodoperfluorohexane, 1,8-diiodoperfluorooctane, 1,12-diiodoperfluorododecane, 1,16-diiodoperfluorohexadecane, diiodomethane, 1,2-diiodoethane, 1,3-diiodo-n-propane, CF ₂ Br ₂ , BrCF ₂ CF ₂ Br, CF ₃ CFBrCF ₂ Br, CFClBr ₂ , BrCF ₂ CFClBr, CFBrClCFClBr, BrCF ₂ CF ₂ Examples of such compounds include CF ₂ Br, BrCF ₂ CFBrOCF ₃ , 1-bromo-2-iodoperfluoroethane, 1-bromo-3-iodoperfluoropropane, 1-bromo-4-iodoperfluorobutane, 2-bromo-3-iodoperfluorobutane, 3-bromo-4-iodoperfluorobutene-1, 2-bromo-4-iodoperfluorobutene-1, monoiodomonobromo-substituted benzene, diiodomonobromo-substituted benzene, and (2-iodoethyl) and (2-bromoethyl)-substituted benzene. These compounds may be used alone or in combination with each other.

Among these, it is preferable to use 1,4-diiodoperfluorobutane, 1,6-diiodoperfluorohexane, and 2-iodoperfluoropropane in terms of polymerization reactivity, crosslinking reactivity, and availability.

The fluororubber described above can be manufactured by conventional methods.

(b) Crosslinking Agent The fluororubber crosslinking composition of the present disclosure contains a crosslinking agent.

In one embodiment, the first crosslinker is:
1) at least one aromatic ring;
2) a group having a carbon-carbon double bond (excluding those constituting the aromatic ring), and
3) A compound having an alkylcarbonyloxy group in the molecule directly bonded to a carbon atom constituting the aromatic ring is used.

The aromatic ring may be either a monocyclic or polycyclic ring. The aromatic ring may be a so-called heterocyclic ring composed of not only carbon atoms but also carbon atoms and heteroatoms such as oxygen atoms, sulfur atoms, and nitrogen atoms. In the aromatic ring, the carbon atom of the carbonyl group may form a ring structure.

Examples of monocyclic aromatic rings include monocyclic 5- to 7-membered aromatic rings, and specifically, preferred are a benzene ring and a monocyclic 5- to 7-membered aromatic heterocycle (including a 7-membered ring with a tropone structure), more preferred are a benzene ring, a furan ring, and a thiophene ring, and even more preferred is a benzene ring.

The number of aromatic rings in the polycyclic aromatic ring is 2 or more, preferably 2 to 8, more preferably 2 to 4, even more preferably 2 or 3, and particularly preferably 2.

As the polycyclic aromatic ring, a polycyclic aromatic hydrocarbon ring or a polycyclic aromatic heterocycle is preferred, and a polycyclic aromatic hydrocarbon ring is more preferred. The polycyclic aromatic hydrocarbon ring may be a polycycle in which two rings are linked via a bond, a condensed ring, or a spiro ring.

The number of carbon atoms in the polycyclic aromatic hydrocarbon ring is preferably 3 to 30, more preferably 5 or more, even more preferably 6 or more, more preferably 20 or less, even more preferably 14 or less.

The number of rings in the polycyclic aromatic hydrocarbon ring is preferably 2 to 4, more preferably 2 or 3, and even more preferably 2.

Polycyclic aromatic hydrocarbon rings include:
Polycyclic aromatic hydrocarbon rings in which two rings are linked via a bond, such as a biphenyl ring, a diphenylmethane ring, a diphenyl ether ring, a diphenyl sulfone ring, or a diphenyl ketone ring;
condensed polycyclic hydrocarbon rings such as a naphthalene ring, a phenanthrene ring, an anthracene ring, a fluorene ring, a tetracene ring, a chrysene ring, a pyrene ring, a pentacene ring, a benzopyrene ring, a triphenylene ring, and an azulene ring;
etc.

As the polycyclic aromatic hydrocarbon ring, a naphthalene ring or a biphenyl ring is preferable.

In polycyclic aromatic heterocycles, the carbonyl group may form part of the aromatic ring. Polycyclic aromatic heterocycles also include rings that are composed only of carbon atoms and oxygen atoms of carbonyl groups.

As a polycyclic aromatic heterocycle, a ring formed by carbon atoms and atoms other than carbon atoms is preferable. As the atom other than carbon atoms, a nitrogen atom, an oxygen atom, or a sulfur atom is preferable, and an oxygen atom or a sulfur atom is more preferable. That is, as a heterocycle, a nitrogen-containing heterocycle, an oxygen-containing heterocycle, or a sulfur-containing heterocycle is preferable, and an oxygen-containing heterocycle or a sulfur-containing heterocycle is more preferable. The number of atoms other than carbon atoms in the ring is preferably 1 to 3.

The number of rings in the polycyclic aromatic heterocycle is preferably 2 to 4, more preferably 2 or 3, and even more preferably 2.

The polycyclic aromatic heterocycle is preferably an oxygen-containing polycyclic aromatic heterocycle, such as a xanthene ring, a 1-benzopyran ring, a 2-benzopyran ring, a 1-benzofuran ring, or a 2-benzofuran ring.

The aromatic ring is preferably a benzene ring, a naphthalene ring, or a biphenyl ring, since this allows for a molded product with a higher crosslink density and superior tensile strength to be obtained.

The first crosslinking agent has a group having a carbon-carbon double bond in addition to an aromatic ring. The group having a carbon-carbon double bond includes a vinyl group as well as a group that contains a carbon-carbon double bond as part of its structure, such as an allyl group. The number of groups having a carbon-carbon double bond is preferably 1 or more, more preferably 1 or 2, and even more preferably 1.

The group having a carbon-carbon double bond may be directly bonded to a carbon atom constituting the aromatic ring, or may be bonded to a carbon atom constituting the aromatic ring via another bond. It is preferable that the group having a carbon-carbon double bond is directly bonded to a carbon atom constituting the aromatic ring, since this allows for the production of molded products with a higher crosslink density and superior tensile strength.

As the group having a carbon-carbon double bond, at least one selected from the group consisting of a vinyl group, an allyl group, and a vinyloxy group is preferred, since it is possible to obtain a molded article having a higher crosslink density and superior tensile strength, and at least one selected from the group consisting of a vinyl group and an allyl group is more preferred.

As the alkylcarbonyloxy group, a group represented by the general formula:
R-C(=O)-O-
(wherein R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms) is preferred. The number of carbon atoms in the alkyl group and the fluorinated alkyl group is preferably 1 to 3, and more preferably 1. R is preferably a methyl group.

The hydrogen atom bonded to the carbon atom constituting the aromatic ring may be substituted with a substituent other than a group having a carbon-carbon double bond and an alkylcarbonyloxy group. As such a substituent, a substituent (γ) (excluding substituents containing a hydroxyl group and alkylcarbonyloxy groups) in which at least one of the values of Hammett's substituent constants σm and σp is 0.03 or more is preferable. By directly bonding the substituent (γ) to the carbon atom constituting the aromatic ring, the electron density of the alkylcarbonyloxy group bonded directly to the carbon atom constituting the aromatic ring can be appropriately adjusted, thereby improving the properties of the molded article obtained from the fluororubber crosslinking composition.

The substituent (γ) does not include substituents containing a hydroxy group or alkylcarbonyloxy groups. Substituents containing a hydroxy group include hydroxy groups and groups that have a hydroxy group as part of their structure.

The number of substituents (γ) is preferably 0 to 4, more preferably 0 to 2, and even more preferably 0 or 1.

The substituent (γ) is a monovalent substituent in which at least one of the Hammett substituent constants σm and σp is in the range of 0.03 or more.

At least one of the substituent constants σm and σp of the substituent (γ) is 0.03 or more, preferably 0.05 or more, more preferably 0.10 or more, preferably 1.40 or less, more preferably 1.00 or less, and even more preferably 0.80 or less.

In one embodiment, the value of the substituent constant σm of the substituent (γ) is 0.03 or more, preferably 0.05 or more, more preferably 0.10 or more, preferably 1.40 or less, more preferably 1.00 or less, and even more preferably 0.80 or less.

In one embodiment, the value of the substituent constant σp of the substituent (γ) is 0.03 or more, preferably 0.05 or more, more preferably 0.10 or more, preferably 1.40 or less, more preferably 1.00 or less, and even more preferably 0.80 or less.

Hammett's rule is an empirical rule proposed by L. P. Hammett in 1935 to quantitatively discuss the effect of substituents on the reaction or equilibrium of benzene derivatives, and is widely recognized as valid today. The substituent constants determined by Hammett's rule include σp and σm values, and these values can be found in many general textbooks, but in this invention, the values described in "TABLE 1 Hammett and Modified Swain-Lupton Constants" in Chem. Rev., 1991, Vol. 91, pp. 165-195 are used. For substituents not described in the above literature, values calculated according to the calculation method described in the literature "The Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives" (J. Am. Chem. Soc. 1937, 59, 1, 96-103) are used.

The first crosslinking agent also includes those that are not benzene derivatives, but the σm value and σp value are used as a measure of the electronic effect of the substituent, regardless of the substitution position. In this disclosure, the σm value and σp value are used in this sense.

Specific examples of the substituent (γ) include partially fluorinated alkyl groups having 1 to 5 carbon atoms, perfluoroalkyl groups having 1 to 5 carbon atoms, fluorine atoms, chlorine atoms, alkoxycarbonyl groups having 1 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group), partially fluorinated alkoxycarbonyl groups having 1 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group), perfluoroalkoxycarbonyl groups having 1 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group), alkoxy groups having 1 to 5 carbon atoms, partially fluorinated alkoxy groups having 1 to 5 carbon atoms, perfluoroalkoxy groups having 1 to 5 carbon atoms, and alkoxy groups having 1 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group). Examples of such groups include acyloxy groups with 1 to 5 carbon atoms (excluding the number of carbon atoms that make up the carbonyl group) in which some of the carbon atoms are fluorinated, perfluoroacyloxy groups with 1 to 5 carbon atoms (excluding the number of carbon atoms that make up the carbonyl group), acyl groups with 0 to 5 carbon atoms (excluding the number of carbon atoms that make up the carbonyl group), acyl groups with 0 to 5 carbon atoms (excluding the number of carbon atoms that make up the carbonyl group) in which some of the carbon atoms are fluorinated, perfluoroacyl groups with 0 to 5 carbon atoms (excluding the number of carbon atoms that make up the carbonyl group), alkylsulfonyl groups with 1 to 5 carbon atoms, alkylsulfonyl groups with 1 to 5 carbon atoms in which some of the carbon atoms are fluorinated, perfluoroalkylsulfonyl groups with 1 to 5 carbon atoms, and trimethoxysilyl groups.

As the substituent (γ), at least one selected from the group consisting of a partially fluorinated alkyl group having 1 to 5 carbon atoms, a perfluoroalkyl group having 1 to 5 carbon atoms, a fluorine atom, a chlorine atom, an alkoxy group having 1 to 5 carbon atoms, an alkoxycarbonyl group having 0 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group), and an acyl group having 0 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group) is preferred, and at least one selected from the group consisting of a perfluoroalkyl group having 1 to 5 carbon atoms, a fluorine atom, a chlorine atom, an alkoxy group having 1 to 5 carbon atoms, an alkoxycarbonyl group having 0 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group), and and at least one selected from the group consisting of acyl groups having 0 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group), more preferably at least one selected from the group consisting of perfluoroalkyl groups having 1 to 5 carbon atoms, fluorine atoms, chlorine atoms, and acyl groups having 0 to 5 carbon atoms (excluding the number of carbon atoms constituting the carbonyl group), even more preferably at least one selected from the group consisting of chlorine atoms, fluorine atoms, acetyl groups, methoxycarbonyl groups, and methoxy groups, and particularly preferably at least one selected from the group consisting of acetyl groups and methoxycarbonyl groups.

The hydrogen atoms bonded to the carbon atoms constituting the aromatic ring of the first crosslinking agent may or may not be substituted with any substituent other than the substituent (γ), but it is preferable that they are not substituted with any substituent other than the substituent (γ) so as not to impair the function of the substituent (γ) that gives the hydroxy group an appropriate electron density. In one embodiment, the aromatic ring of the crosslinking agent is not substituted with any substituent other than a group having a carbon-carbon double bond and an alkylcarbonyloxy group.

As the first crosslinking agent, at least one selected from the group consisting of compounds represented by general formulas (b1) to (b3) is preferred, at least one selected from the group consisting of compounds represented by general formulas (b1) to (b2) is more preferred, a compound represented by general formula (b1) is even more preferred, and at least one selected from the group consisting of 4-vinylphenyl acetate and 4-allylphenol is particularly preferred, since this allows for the production of molded products with a higher crosslinking density and superior tensile strength.

（式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基、Ｘは、ビニル基、アリル基またはビニルオキシ基、Ｙは、Ｈ、または、Ｈａｍｍｅｔｔの置換基定数σｍおよびσｐの少なくとも一方の値が、０．０３以上である置換基（γ）（ただしヒドロキシ基を含有する置換基およびアルキルカルボニルオキシ基を除く）である） General formula (b1):

(In the formula, R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms; X is a vinyl group, an allyl group, or a vinyloxy group; Y is H, or a substituent (γ) having at least one of the Hammett substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxy group and alkylcarbonyloxy groups).)

（式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基、Ｘは、ビニル基、アリル基またはビニルオキシ基、ＹおよびＺは、それぞれ独立して、Ｈ、または、Ｈａｍｍｅｔｔの置換基定数σｍおよびσｐの少なくとも一方の値が、０．０３以上である置換基（γ）（ただしヒドロキシ基を含有する置換基およびアルキルカルボニルオキシ基を除く）である） General formula (b2):

(In the formula, R represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms; X represents a vinyl group, an allyl group, or a vinyloxy group; Y and Z each independently represent H or a substituent (γ) having at least one of the Hammett substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxy group and alkylcarbonyloxy groups).

（式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基、Ｘは、ビニル基、アリル基またはビニルオキシ基、ＹおよびＺは、それぞれ独立して、Ｈ、または、Ｈａｍｍｅｔｔの置換基定数σｍおよびσｐの少なくとも一方の値が、０．０３以上である置換基（γ）（ただしヒドロキシ基を含有する置換基およびアルキルカルボニルオキシ基を除く）、Ａは、結合手、炭素数１～１３のアルキレン基、炭素数６～１３のアリーレン基、チオカルボニル基、酸素原子、カルボニル基、スルフィニル基またはスルホニル基、Ａのアルキレン基およびアリーレン基は、炭素原子に結合した水素原子の一部または全部が塩素原子またはフッ素原子により置換されていてもよい、環Ｂおよび環Ｃは、それぞれ独立して、単環または多環の芳香族環である） General formula (b3):

(wherein R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms or a fluorinated alkyl group having 1 to 5 carbon atoms; X is a vinyl group, an allyl group or a vinyloxy group; Y and Z are each independently H or a substituent (γ) having at least one value of Hammett's substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxyl group and alkylcarbonyloxy groups); A is a bond, an alkylene group having 1 to 13 carbon atoms, an arylene group having 6 to 13 carbon atoms, a thiocarbonyl group, an oxygen atom, a carbonyl group, a sulfinyl group or a sulfonyl group; in the alkylene group and arylene group of A, some or all of the hydrogen atoms bonded to carbon atoms may be substituted with chlorine atoms or fluorine atoms; and ring B and ring C are each independently a monocyclic or polycyclic aromatic ring.)

In the same formula, Y and Z may be the same or different. In addition, in general formulas (b1) to (b3), R, X, Y, and Z are each independent, and therefore R, X, Y, and Z in the three general formulas may be different for each general formula.

In general formulas (b1) to (b3), R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms. The number of carbon atoms in the alkyl group and fluorinated alkyl group of R is preferably 1 to 3, and more preferably 1. R is preferably a methyl group.

In general formulas (b1) to (b3), X is a vinyl group, an allyl group, or a vinyloxy group. X is preferably a vinyl group or an allyl group.

In the general formulas (b1) to (b3), Y is H or a substituent (γ) in which at least one of the Hammett substituent constants σm and σp is 0.03 or more (excluding substituents containing a hydroxyl group and alkylcarbonyloxy groups). The substituent (γ) is as described above.

Y is preferably at least one selected from the group consisting of a hydrogen atom, a chlorine atom, a fluorine atom, an acetyl group, a methoxycarbonyl group, and a methoxy group, more preferably at least one selected from the group consisting of a hydrogen atom, an acetyl group, and a methoxycarbonyl group, even more preferably at least one selected from the group consisting of a hydrogen atom, an acetyl group, and a methoxycarbonyl group, and particularly preferably a hydrogen atom.

In the general formulas (b2) to (b3), Z is H or a substituent (γ) in which at least one of the Hammett substituent constants σm and σp is 0.03 or more (excluding substituents containing a hydroxyl group and alkylcarbonyloxy groups). The substituent (γ) is as described above.

Z is preferably at least one selected from the group consisting of a hydrogen atom, a chlorine atom, a fluorine atom, an acetyl group, a methoxycarbonyl group, and a methoxy group, more preferably at least one selected from the group consisting of a hydrogen atom, an acetyl group, and a methoxycarbonyl group, even more preferably at least one selected from the group consisting of a hydrogen atom, an acetyl group, and a methoxycarbonyl group, and particularly preferably a hydrogen atom.

In general formula (b3), A represents the type of bond connecting the two aromatic rings, and is a bond, an alkylene group having 1 to 13 carbon atoms, an arylene group having 6 to 13 carbon atoms, a thiocarbonyl group, an oxygen atom, a carbonyl group, a sulfinyl group, or a sulfonyl group. In the alkylene group and arylene group of A, some or all of the hydrogen atoms bonded to the carbon atoms may be replaced by chlorine atoms or fluorine atoms.

A is preferably a bond or an alkylene group having 1 to 13 carbon atoms, more preferably a bond.

Ring B and ring C are each independently a monocyclic or polycyclic aromatic ring. The aromatic ring may be a so-called heterocyclic ring composed of not only carbon atoms but also carbon atoms and heteroatoms such as oxygen atoms, sulfur atoms, and nitrogen atoms. The carbon atom of the carbonyl group may also constitute a ring structure.

As ring B and ring C, a monocyclic ring is preferred, since it allows the production of a molded product with a higher crosslink density and superior tensile strength, a monocyclic 5- to 7-membered aromatic ring is more preferred, a benzene ring and a monocyclic 5- to 7-membered aromatic heterocycle (including a 7-membered ring with a tropone structure) are even more preferred, a benzene ring, a furan ring and a thiophene ring are even more preferred, and a benzene ring is particularly preferred.

In general formula (b3), it is preferable that rings B and C are both benzene rings, since this allows for a molded article to be obtained that has a higher crosslink density and is more excellent in tensile strength. In other words, the compound (b3) represented by general formula (b3) is preferably a compound represented by general formula (b3-1).

（式中、Ｒ、Ｘ、Ｙ、ＺおよびＡは上記したとおりである） General formula (b3-1):

(In the formula, R, X, Y, Z and A are as defined above.)

（各式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基である） In one embodiment, at least one selected from the group consisting of compounds represented by formulae (b4) to (b7) is used as the second crosslinking agent.

(In each formula, R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms.)

The compounds represented by formulae (b4) to (b7) do not have any other substituents than a hydroxy group, a group having a carbon-carbon double bond (excluding those constituting an aromatic ring), and an alkylcarbonyloxy group represented by -OC(=O)R.

Although the compounds represented by formulae (b4) and (b5) do not have a double bond and an aromatic ring to which an alkylcarbonyloxy group is bonded, when used as a crosslinking agent, they smoothly promote the crosslinking reaction of the fluororubber, as do the compounds represented by formulae (b6) and (b7), and provide molded products with high crosslink density and excellent tensile strength.

As the second crosslinking agent, at least one selected from the group consisting of compounds represented by formula (b5) and formula (b6) is preferred.

The content of the crosslinking agent is preferably 0.1 to 10 parts by mass, more preferably 0.5 parts by mass or more, even more preferably 0.7 parts by mass or more, more preferably 7 parts by mass or less, and even more preferably 5 parts by mass or less, so that the crosslinking reaction in the crosslinking step proceeds at an appropriate speed and a molded product having sufficient tensile strength, elongation at break, and compression set properties at high temperatures, as well as appropriate hardness, can be obtained.

(c) Dehydrofluorination Agent The fluororubber crosslinking composition of the present disclosure contains a dehydrofluorination agent. The use of the dehydrofluorination agent can promote the formation of an intramolecular double bond in the dehydrofluorination reaction of the fluororubber main chain, thereby promoting the crosslinking reaction.

As the dehydrofluorination agent, an onium compound is generally used. There is no particular limitation on the onium compound, and examples thereof include ammonium salts such as quaternary ammonium salts, phosphonium salts such as quaternary phosphonium salts, and sulfonium salts, among which quaternary ammonium salts and quaternary phosphonium salts are preferred.

The quaternary ammonium salt is not particularly limited, and examples thereof include 8-methyl-1,8-diazabicyclo[5,4,0]-7-undecenium chloride, 8-methyl-1,8-diazabicyclo[5,4,0]-7-undecenium iodide, 8-methyl-1,8-diazabicyclo[5,4,0]-7-undecenium hydroxide, and 8-methyl-1,8-diazabicyclo[5,4,0]-7-undecenium methylsulfate. , 8-ethyl-1,8-diazabicyclo[5,4,0]-7-undecenium bromide, 8-propyl-1,8-diazabicyclo[5,4,0]-7-undecenium bromide, 8-dodecyl-1,8-diazabicyclo[5,4,0]-7-undecenium chloride, 8-dodecyl-1,8-diazabicyclo[5,4,0]-7-undecenium hydroxide, 8-eicosyl-1,8-diazabicyclo[5,4,0]-7 -undecenium chloride, 8-tetracosyl-1,8-diazabicyclo[5,4,0]-7-undecenium chloride, 8-benzyl-1,8-diazabicyclo[5,4,0]-7-undecenium chloride (hereinafter referred to as DBU-B), 8-benzyl-1,8-diazabicyclo[5,4,0]-7-undecenium hydroxide, 8-phenethyl-1,8-diazabicyclo[5,4,0]-7-undecenium chloride, 8-(3-phenylpropyl)-1,8-diazabicyclo[5,4,0]-7-undecenium chloride, benzyldimethyloctadecylammonium chloride, tetrabutylammonium bromide, tetrabutylammonium chloride, benzyltributylammonium chloride, benzyltriethylammonium chloride, tetrabutylammonium hydrogen sulfate, and tetrabutylammonium hydroxide. Among these, DBU-B or benzyldimethyloctadecylammonium chloride are preferred in terms of crosslinking properties and physical properties of the crosslinked product.

The quaternary phosphonium salt is not particularly limited, and examples thereof include tetrabutylphosphonium chloride, benzyltriphenylphosphonium chloride (hereinafter referred to as BTPPC), benzyltrimethylphosphonium chloride, benzyltributylphosphonium chloride, tributylallylphosphonium chloride, tributyl-2-methoxypropylphosphonium chloride, and benzylphenyl(dimethylamino)phosphonium chloride. Among these, benzyltriphenylphosphonium chloride (BTPPC) is preferred in terms of crosslinkability and physical properties of the crosslinked product.

The content of the dehydrofluorination agent is preferably 0.1 to 10 parts by mass, more preferably 0.1 to 5 parts by mass, even more preferably 0.1 to 3 parts by mass, and particularly preferably 0.1 to 1.5 parts by mass, per 100 parts by mass of fluororubber, because the crosslinking reaction proceeds at an appropriate speed and the compression set properties at high temperatures make it possible to obtain a molded product with even better properties.

(d) Organic Peroxide The fluororubber crosslinking composition of the present disclosure contains an organic peroxide.

As the organic peroxide, those which easily generate peroxy radicals in the presence of heat or an oxidation-reduction system are preferred. Specific examples include 1,1-bis(t-butylperoxy)-3,5,5-trimethylcyclohexane, 2,5-dimethylhexane-2,5-dihydroperoxide, di-t-butyl peroxide, t-butylcumyl peroxide, dicumyl peroxide, α,α'-bis(t-butylperoxy)-p-diisopropylbenzene, 2,5-dimethyl-2,5-bis(t-butylperoxy)hexane, 2,5-dimethyl-2,5-bis(t-butylperoxy)-hexyne-3, benzoyl peroxide, t-butylperoxybenzene, 2,5-dimethyl-2,5-di(benzoylperoxy)hexane, t-butylperoxymaleic acid, t-butylperoxyisopropylcarbonate, and t-butylperoxybenzoate. Among these, 2,5-dimethyl-2,5-bis(t-butylperoxy)hexane and 2,5-dimethyl-2,5-bis(t-butylperoxy)-hexyne-3 are preferred.

The content of organic peroxide is preferably 0.05 to 10 parts by mass, more preferably 0.1 part by mass or more, more preferably 5 parts by mass or less, and even more preferably 1 part by mass or less, per 100 parts by mass of fluororubber, since a molded product with a higher crosslink density and superior tensile strength can be obtained.

(e) Acid Acceptor The fluororubber crosslinking composition of the present disclosure may further contain an acid acceptor. By containing an acid acceptor, the crosslinking reaction of the fluororubber crosslinking composition proceeds more smoothly, and the compression set properties at high temperatures are further improved.

Examples of acid acceptors include metal oxides such as magnesium oxide, calcium oxide, bismuth oxide, and zinc oxide; metal hydroxides such as calcium hydroxide; alkali metal silicates such as hydrotalcite and sodium metasilicate, which are described in JP-T-2011-522921; and metal salts of weak acids such as those described in JP-A-2003-277563. Examples of metal salts of weak acids include carbonates, benzoates, oxalates, and phosphites of Ca, Sr, Ba, Na, and K.

As the acid acceptor, at least one selected from the group consisting of metal oxides, metal hydroxides, alkali metal silicates, metal salts of weak acids, and hydrotalcite is preferred, since it is possible to obtain molded articles with better compression set properties at high temperatures, and at least one selected from the group consisting of sodium metasilicate hydrate, calcium hydroxide, magnesium oxide, bismuth oxide, and hydrotalcite is more preferred. Furthermore, when the molded article to be obtained requires good water resistance, acid resistance, or resistance to organic acid esters including biodiesel, at least one selected from the group consisting of bismuth oxide and hydrotalcite is preferred as the acid acceptor.

In the fluororubber crosslinking composition, the content of the acid acceptor is preferably 0.1 to 100 parts by mass, more preferably 1 to 50 parts by mass, even more preferably 1 to 30 parts by mass, and particularly preferably 1 to 20 parts by mass, per 100 parts by mass of the fluororubber, since this allows for the production of molded products with even better compression set properties at high temperatures.

When the content of the acid acceptor is high, the water resistance, acid resistance, and resistance to organic acid esters, including biodiesel, of the resulting molded article tend to decrease, while when the content of the acid acceptor is low, the crosslinking speed decreases and the mechanical properties tend to decrease due to the decrease in crosslink density. Therefore, the content of the acid acceptor can be selected according to the application of the resulting molded article. When an acid acceptor other than calcium hydroxide is contained, the content of calcium hydroxide can be reduced to 0 to 1.5 parts by mass, and the content of the other acid acceptor can be adjusted to adjust the crosslink density, thereby obtaining a molded article with better compression set properties at high temperatures.

(f) Other Components The fluororubber crosslinking composition may be blended with various additives as necessary, such as usual additives blended in fluororubber crosslinking compositions, for example, fillers (carbon black, bituminous coal, barium sulfate, diatomaceous earth, calcined clay, talc, wollastonite, carbon nanotubes, etc.), processing aids (waxes, etc.), plasticizers, colorants, stabilizers, tackifiers (coumarone resins, coumarone-indene resins, etc.), release agents, electrical conductivity imparting agents, thermal conductivity imparting agents, surface non-tackifiers, flexibility imparting agents, heat resistance improving agents, flame retardants, foaming agents, and antioxidants described in WO 2012/023485, and may also be blended with one or more usual crosslinking agents and dehydrofluorination agents different from the above.

Of these, the preferred carbon blacks are thermal carbon black and furnace carbon black, with MT carbon black, FT carbon black and SRF carbon black being more preferred. When carbon black or carbon black with a relatively large particle size such as FT carbon black is blended, molded products with excellent compression set properties are obtained, while when carbon black with a fine particle size is blended, molded products with excellent strength and elongation are obtained. By blending different grades together, the above properties can be balanced.

Other fillers than carbon black include barium sulfate and wollastonite.

Processing aids are not particularly limited, but may include, for example, aliphatic amines such as stearylamine, fatty acid esters such as stearic acid esters and sebacic acid esters, fatty acid amides such as stearic acid amide, long-chain alkyl alcohols, natural waxes, polyethylene waxes, phosphate esters such as tricresyl phosphate, silicone-based processing aids, etc., and blending two or more types in appropriate amounts as necessary can improve the balance between mold releasability during molding and the physical properties of the molded product.

The content of the filler such as carbon black is not particularly limited, but is preferably 0 to 300 parts by mass, more preferably 1 to 150 parts by mass, even more preferably 2 to 100 parts by mass, and particularly preferably 2 to 75 parts by mass, per 100 parts by mass of the fluororubber.

The content of processing aids such as wax is preferably 0 to 10 parts by mass, more preferably 0 to 5 parts by mass, and particularly preferably 0 to 2 parts by mass, per 100 parts by mass of fluororubber. The use of processing aids, plasticizers, and release agents tends to reduce the mechanical properties and sealing properties of the resulting molded product, so it is necessary to adjust the content of these agents within a range that allows the desired properties of the resulting molded product.

The fluororubber crosslinking composition may contain a dialkyl sulfone compound. By containing a dialkyl sulfone compound, the crosslinking efficiency of the fluororubber crosslinking composition is increased, the crosslinking speed is increased, the compression set property is further improved, and the fluidity of the rubber material is improved. Examples of dialkyl sulfone compounds include dimethyl sulfone, diethyl sulfone, dibutyl sulfone, methyl ethyl sulfone, diphenyl sulfone, and sulfolane. Among them, sulfolane is preferred from the viewpoint of crosslinking efficiency and compression set property, and because it has an appropriate boiling point. The content of the dialkyl sulfone compound is preferably 0 to 10 parts by mass, more preferably 0 to 5 parts by mass, and particularly preferably 0 to 3 parts by mass, per 100 parts by mass of the fluororubber. When the fluororubber crosslinking composition of the present disclosure contains a dialkyl sulfone compound, the lower limit of the content of the dialkyl sulfone compound may be, for example, 0.1 parts by mass or more per 100 parts by mass of the fluororubber.

The dialkyl sulfone compound and the processing aid may be blended together, as this provides a good balance between the crosslinking rate, the fluidity of the rubber material during molding, the mold releasability during molding, and the mechanical properties of the molded product.

The fluororubber crosslinking composition is obtained by kneading the fluororubber (a), the crosslinking agent (b), the dehydrofluorination agent (c), the organic peroxide (d), etc., using a commonly used rubber kneading device. Examples of the rubber kneading device that can be used include a roll, a kneader, a Banbury mixer, an internal mixer, and a twin-screw extruder.

In order to disperse each component uniformly in the rubber, some of the components may be kneaded while melting them at a high temperature of 100 to 200°C using a closed kneading device such as a kneader, and then the remaining components may be kneaded at a relatively low temperature below this temperature.

In addition, the dispersibility can be further improved by mixing the fluororubber (a), crosslinking agent (b), dehydrofluorination agent (c), organic peroxide (d), etc., leaving the mixture at room temperature for 12 hours or more, and then mixing again.

<Molded products>
The molded article of the present disclosure can be obtained by crosslinking the fluororubber crosslinking composition. The molded article of the present disclosure can also be obtained by molding and crosslinking the fluororubber crosslinking composition. The fluororubber crosslinking composition can be molded by a conventionally known method. The molding and crosslinking methods and conditions may be within the range of known methods and conditions for the molding and crosslinking to be adopted. The order of molding and crosslinking is not limited, and molding may be followed by crosslinking, crosslinking may be followed by molding, or molding and crosslinking may be performed simultaneously.

Examples of molding methods include, but are not limited to, compression molding, casting, injection molding, extrusion molding, and roto-cure molding. Examples of crosslinking methods that can be used include steam crosslinking, heat crosslinking, and radiation crosslinking, with steam crosslinking and heat crosslinking being preferred. Specific crosslinking conditions that are not limited to these are usually within a temperature range of 140 to 250°C and a crosslinking time of 1 minute to 24 hours, and can be determined appropriately depending on the types of crosslinking agent (b), dehydrofluorination agent (c), organic peroxide (d), acid acceptor (e), etc.

In addition, by heating the obtained molded product in an oven or the like, it is possible to improve mechanical properties such as tensile strength, heat resistance, and compression set properties at high temperatures. Specific crosslinking conditions, which are not limited, are usually in the temperature range of 140 to 300°C, in the range of 30 minutes to 72 hours, and can be appropriately determined depending on the types of crosslinking agent (b), dehydrofluorination agent (c), organic peroxide (d), etc.

The molded article of the present disclosure has excellent properties such as heat resistance, oil resistance, chemical resistance, and flexibility, and further has excellent compression set properties at high temperatures. Therefore, the molded article of the present disclosure is generally used in areas that come into contact with other materials and slide, seal or enclose other materials or substances, and are intended for vibration and soundproofing, and can be used as various parts in various fields such as the automotive industry, the aircraft industry, and the semiconductor industry.

Fields in which they are used include, for example, semiconductor-related fields, automobiles, aircraft, space and rockets, ships, chemicals such as chemical plants, pharmaceuticals such as medicines, photography such as developing machines, printing such as printing machines, painting such as painting equipment, analytical and physicochemical machinery such as analytical instruments and gauges, food equipment including food plant equipment and household goods, food beverage manufacturing equipment, pharmaceutical manufacturing equipment, medical parts, chemical transport equipment, nuclear power plant equipment, steel such as steel processing equipment, general industry, electricity, fuel cells, electronic parts, optical equipment parts, space equipment parts, petrochemical plant equipment, energy resource exploration and mining equipment parts for oil and gas, oil refining, and oil transport equipment parts.

Examples of uses for molded products include various sealing materials and packings such as rings, packings, gaskets, diaphragms, oil seals, bearing seals, lip seals, plunger seals, door seals, lip and face seals, gas delivery plate seals, wafer support seals, and barrel seals. As sealing materials, they can be used in applications requiring heat resistance, solvent resistance, chemical resistance, and non-stickiness.

It can also be used for tubes, hoses, rolls, various rubber rolls, flexible joints, rubber sheets, coatings, belts, dampers, valves, valve seats, valve bodies, chemical-resistant coating materials, laminating materials, lining materials, etc.

The cross-sectional shape of the rings, packings, and seals may be of various shapes, such as a square, O-shape, or ferrule shape, or an irregular shape such as a D-shape, L-shape, T-shape, V-shape, X-shape, or Y-shape.

In the above-mentioned semiconductor-related fields, the present invention can be used, for example, in semiconductor manufacturing equipment, liquid crystal panel manufacturing equipment, plasma panel manufacturing equipment, plasma display panel manufacturing equipment, plasma addressed liquid crystal panel manufacturing equipment, organic EL panel manufacturing equipment, field emission display panel manufacturing equipment, solar cell substrate manufacturing equipment, semiconductor conveying equipment, and the like. Examples of such equipment include CVD equipment, gas control equipment such as semiconductor gas control equipment, dry etching equipment, wet etching equipment, plasma etching equipment, reactive ion etching equipment, reactive ion beam etching equipment, sputter etching equipment, ion beam etching equipment, oxidation diffusion equipment, sputtering equipment, ashing equipment, plasma ashing equipment, cleaning equipment, ion implantation equipment, plasma CVD equipment, exhaust equipment, exposure equipment, polishing equipment, film formation equipment, dry etching cleaning equipment, UV/ _O3 cleaning equipment, ion beam cleaning equipment, laser beam cleaning equipment, plasma cleaning equipment, gas etching cleaning equipment, extraction cleaning equipment, Soxhlet extraction cleaning equipment, high temperature and high pressure extraction cleaning equipment, microwave extraction cleaning equipment, supercritical extraction cleaning equipment, cleaning equipment using hydrofluoric acid, hydrochloric acid, sulfuric acid, ozone water, etc., steppers, coater developers, CMP equipment, excimer laser exposure equipment, chemical liquid piping, gas piping, _NF3 plasma processing, O Examples of such equipment include equipment for performing plasma treatment such as _{No. 2} plasma treatment and fluorine plasma treatment, heat treatment film formation equipment, wafer transport equipment, wafer cleaning equipment, silicon wafer cleaning equipment, silicon wafer processing equipment, equipment used in LP-CVD processes, equipment used in lamp annealing processes, and equipment used in reflow processes.

Specific uses in the semiconductor-related field include, for example, various sealing materials such as O-rings and gaskets for gate valves, quartz windows, chambers, chamber lits, gates, bell jars, couplings, and pumps; various sealing materials such as O-rings for resist developer and stripper solutions, hoses and tubes; linings and coatings for resist developer tanks, stripper tanks, wafer cleaning solution tanks, and wet etching tanks; pump diaphragms; rolls for transporting wafers; hose tubes for wafer cleaning solutions; clean equipment sealing materials such as sealants for clean equipment in clean rooms, etc.; sealing materials for storage facilities that store semiconductor manufacturing equipment and devices such as wafers; and diaphragms for transporting chemicals used in the semiconductor manufacturing process.

In the above-mentioned automotive field, it can be used in the engine body, main motion system, valve system, lubrication and cooling system, fuel system, intake and exhaust system, drive transmission system, chassis steering system, brake system, basic electrical components, control system electrical components, equipment electrical components, and other electrical components. Note that the above-mentioned automotive field also includes motorcycles.

In the engine body and its peripheral devices as described above, molded products can be used for various sealing materials that require heat resistance, oil resistance, fuel oil resistance, engine cooling antifreeze resistance, and steam resistance. Examples of such sealing materials include gaskets, shaft seals, valve stem seals, and other seals; self-sealing packings, piston rings, split ring packings, mechanical seals, oil seals, and other non-contact or contact type packings; bellows, diaphragms, hoses, tubes, as well as electrical wires, cushioning materials, vibration-proofing materials, and various sealing materials used in belt AT devices.

Specific uses in the above fuel systems include fuel injectors, cold start injectors, fuel line quick connectors, sender flange quick connectors, fuel pumps, fuel tank quick connectors, gasoline mixing pumps, gasoline pumps, fuel tube bodies, fuel tube connectors, O-rings used in injectors, etc.; intake manifolds, fuel filters, pressure regulating valves, canisters, fuel tank caps, fuel pumps, fuel tanks, fuel tank sender units, fuel injection devices, high pressure fuel pumps, fuel line connector systems, pump timing control valves, suction con Seals used in control valves, solenoid sub-assemblies, fuel cut valves, etc.; canister purge solenoid valve seals, on-board refueling vapor recovery (ORVR) valve seals, oil seals for fuel pumps, fuel sender seals, fuel tank rollover valve seals, filler seals, injector seals, filler cap seals, filler cap valve seals; fuel hoses, fuel supply hoses, fuel return hoses, vapor (evaporation) hoses, vent (breather) hoses, filler hoses, filler neck hoses, hoses inside fuel tanks (in-tank hoses), carburetor con Hoses such as troll hoses, fuel inlet hoses, and fuel breather hoses; gaskets used in fuel filters, fuel line connector systems, and flange gaskets used in carburetors, etc.; line materials such as vapor recovery lines, fuel feed lines, and vapor/ORVR lines; canisters, ORVRs, fuel pumps, fuel tank pressure sensors, gasoline pumps, carburetor sensors, composite air control devices (CACs), pulsation dampers, diaphragms used in canisters, autococks, and pressure regulator diaphragms for fuel injection devices; fuel pump valves, carburetor needle valves, These include rollover check valves, check valves; vents (breathers), tubes used inside fuel tanks; tank gaskets for fuel tanks, gaskets for carburetor acceleration pump pistons; fuel sender vibration isolation parts for fuel tanks; O-rings and diaphragms for controlling fuel pressure; accelerator pump cups; in-tank fuel pump mounts; injector cushion rings for fuel injection systems; injector seal rings; carburetor needle valve core valves; carburetor acceleration pump pistons; valve seats for compound air control systems (CAC); fuel tank bodies; sealing parts for solenoid valves, etc.

Specific uses in the above brake systems include diaphragms used in master bags, hydraulic brake hoses, air brakes, and air brake brake chambers; hoses used in brake hoses, brake oil hoses, vacuum brake hoses, and the like; various sealing materials such as oil seals, O-rings, packing, and brake piston seals; atmospheric valves and vacuum valves for master bags, and check valves for brake valves; piston cups (rubber cups) and brake cups for master cylinders; boots for hydraulic brake master cylinders and vacuum boosters, and wheel cylinders for hydraulic brakes, and O-rings and grommets for anti-lock braking systems (ABS).

Specific examples of uses for the above basic electrical components include insulators and sheaths for electric wires (harnesses), tubes for harness exterior parts, and grommets for connectors.

Specific examples of uses for electrical control components include coating materials for various sensor wires.

Specific examples of uses for the above-mentioned electrical equipment parts include O-rings and packing for car air conditioners, cooler hoses, high-pressure air conditioner hoses, air conditioner hoses, gaskets for electronic throttle units, plug boots for direct ignition, and diaphragms for distributors. It can also be used to bond electrical parts.

Specific examples of uses in the above intake and exhaust systems include packings used in intake manifolds, exhaust manifolds, etc., and throttle body packings for throttles; diaphragms used in EGR (exhaust gas recirculation), pressure control (BPT), wastegates, turbo wastegates, actuators, variable turbine geometry (VTG) turbo actuators, exhaust purification valves, etc.; EGR (exhaust gas recirculation) control hoses, emission control hoses, turbocharger turbo oil hoses (supply), turbo oil hoses (return), turbo air hoses, intercooler hoses, turbocharger hoses, hoses connected to the compressor of turbo engines equipped with intercoolers, exhaust gas hoses, air intake hoses, turbo hoses, DPF (diesel particulate filter) sensor hoses, and other hoses; air ducts and turbo air ducts; intake manifold gaskets; EGR sealing materials, afterburn prevention valve seats for AB valves, turbine shaft seals (for turbochargers, etc.), and sealing materials used in grooved parts such as rocker covers and air intake manifolds used in automobile engines.

Other applications include seals for vapor recovery canisters, catalytic converters, exhaust gas sensors, oxygen sensors, etc. in emission control components, seals for vapor recovery and vapor canister solenoid armatures, intake manifold gaskets, etc.

In diesel engine parts, it can be used as O-ring seals for direct injectors, rotary pump seals, control diaphragms, fuel hoses, EGR, priming pumps, boost compensator diaphragms, etc. It can also be used in O-rings, seal materials, hoses, tubes, diaphragms, gasket materials, and pipes used in urea SCR systems, as well as the urea water tank body and urea water tank seal materials of urea SCR systems.

Specific examples of uses in the above transmission system include transmission-related bearing seals, oil seals, O-rings, packing, torque converter hoses, etc. Other examples include transmission oil seals, AT transmission oil hoses, ATF hoses, O-rings, packing, etc.

Transmission types include AT (automatic transmission), MT (manual transmission), CVT (continuously variable transmission), and DCT (dual clutch transmission).

Other examples include oil seals, gaskets, O-rings, and packing for manual or automatic transmissions, oil seals, gaskets, O-rings, and packing for continuously variable transmissions (belt type or toroidal type), as well as packing for ATF linear solenoids, oil hoses for manual transmissions, ATF hoses for automatic transmissions, and CVTF hoses for continuously variable transmissions (belt type or toroidal type).

Specific examples of uses in steering systems include power steering oil hoses and high-pressure power steering hoses.

Examples of applications in the engine body of an automobile engine include gaskets such as cylinder head gaskets, cylinder head cover gaskets, oil pan packings, and general gaskets, O-rings, packings, seals such as timing belt cover gaskets, hoses such as control hoses, anti-vibration rubber for engine mounts, control valve diaphragms, and camshaft oil seals.

In the main drive system of an automobile engine, it can be used for shaft seals such as crankshaft seals and camshaft seals.

In the valve train of automobile engines, it can be used for valve stem oil seals for engine valves, valve seats for butterfly valves, etc.

In the lubrication and cooling systems of automobile engines, it can be used for engine oil cooler hoses, oil return hoses, seal gaskets for engine oil coolers, water hoses around radiators, radiator seals, radiator gaskets, radiator O-rings, vacuum pump oil hoses for vacuum pumps, as well as radiator hoses, radiator tanks, oil pressure diaphragms, fan coupling seals, etc.

Thus, specific examples of uses in the automotive field include engine head gaskets, oil pan gaskets, manifold packings, oxygen sensor seals, oxygen sensor bushings, nitric oxide (NO _x ) sensor seals, nitric oxide (NO _x ) sensor bushings, sulfur oxide sensor seals, temperature sensor seals, temperature sensor bushings, diesel particle filter sensor seals, diesel particle filter sensor bushings, injector O-rings, injector packings, fuel pump O-rings and diaphragms, gearbox seals, power piston packings, cylinder liner seals, valve stem seals, static valve stem seals, dynamic valve stem seals, automatic transmission front pump seals, rear axle pinion seals, universal joint gaskets, speedometer pinion seals, foot brake piston cups, torque transmission device O-rings and oil seals, exhaust gas re-burning device seals and bearing seals, re-burning device hoses, Carburetor sensor diaphragms, anti-vibration rubber (engine mounts, exhaust parts, muffler hangers, suspension bushings, center bearings, strut bumper rubber, etc.), anti-vibration rubber for suspensions (strut mounts, bushings, etc.), anti-vibration rubber for drive trains (dampers, etc.), fuel hoses, EGR tubes and hoses, twin carb tubes, carburetor needle valve core valves, carburetor flange gaskets, oil hoses, oil cooler hoses, ATF hoses, cylinder head gaskets, water pump seals, gearbox seals, needle valve tips, motorcycle reed valve leads, automobile engine oil seals, gasoline hose gun seals, car air conditioner seals, rubber hoses for engine intercoolers, fuel line connector devices systems), CAC valves, needle tips, engine wiring, filler hoses, car air conditioner O-rings, intake gaskets, fuel tank materials, distributor diaphragms, water hoses, clutch hoses, PS hoses, AT hoses, master back hoses, heater hoses, air conditioner hoses, ventilation hoses, oil filler caps, PS rack seals, rack and pinion boots, CVJ boots, ball joint dust covers, strut dust covers, weather strips, glass runs, centre unit packing, body site welts, bumper rubber, door latches, dash insulators, high tension cords, flat belts, poly V belts, timing belts, toothed belts, V-ribbed belts, tyres, wiper blades, diaphragms and plungers for LPG vehicle regulators, diaphragms and valves for CNG vehicle regulators, rubber parts for DME, diaphragms and boots for auto tensioners, diaphragms and valves for idle speed controls, actuators for auto speed controls, diaphragms, check valves and plungers for vacuum pumps, O.P. Examples of such gaskets include diaphragms and O-rings for S.S., gasoline pressure relief valves, O-rings and gaskets for engine cylinder sleeves, O-rings and gaskets for wet cylinder sleeves, seals and gaskets for differential gears (gear oil seals and gaskets), seals and gaskets for power steering devices (PSF seals and gaskets), seals and gaskets for shock absorbers (SAF seals and gaskets), seals and gaskets for constant velocity joints, seals and gaskets for wheel bearings, coating agents for metal gaskets, caliper seals, boots, wheel bearing seals, and bladders used in the vulcanization molding of tires.

In the aircraft, space and rocket, and marine fields, it can be used particularly in fuel and lubricant systems.

In the aircraft field, for example, they can be used as various sealing parts for aircraft, various aircraft parts for aircraft engine oil applications, jet engine valve stem seals, gaskets and O-rings, rotating shaft seals, gaskets for hydraulic equipment, firewall seals, fuel supply hoses, gaskets and O-rings, aircraft cables, oil seals and shaft seals, etc.

In the space and rocket fields, they can be used, for example, as lip seals, diaphragms, and O-rings for spacecraft, jet engines, missiles, etc., O-rings for oil-resistant gas turbine engines, and vibration isolation pads for missile ground control.

In the marine field, it can be used, for example, as stern seals for screw propeller shafts, intake and exhaust valve stem seals for diesel engines, valve seals for butterfly valves, valve seats and shaft seals for butterfly valves, shaft seals for butterfly valves, stern tube seals, fuel hoses, gaskets, O-rings for engines, cables for ships, oil seals for ships, and shaft seals for ships.

In the chemical industry, such as the above-mentioned chemical plants, and in the pharmaceutical industry, the material can be used in processes that require a high level of chemical resistance, such as processes for manufacturing chemical products such as pharmaceuticals, pesticides, paints, and resins.

Specific uses in the above-mentioned chemical and pharmaceutical fields include chemical equipment, chemical pumps and flow meters, chemical piping, heat exchangers, pesticide sprayers, pesticide transfer pumps, gas piping, fuel cells, analytical equipment and physicochemical equipment (for example, column fittings for analytical equipment and instruments), shrink joints for flue gas desulfurization equipment, nitric acid plants, seals used in power plant turbines, etc., seals used in medical sterilization processes, seals for plating solutions, roller seals for papermaking belts, joint seals for wind tunnels; O-rings used in chemical equipment such as reactors and mixers, analytical equipment and instruments, chemical pumps, pump housings, valves, tachometers, etc., O-rings for mechanical seals, O-rings for compressor sealing; packing used in high-temperature vacuum dryers, tube connections for gas chromatography and pH meters, etc., and glass cooling for sulfuric acid manufacturing equipment. gaskets for diaphragms used in diaphragm pumps, analytical equipment, and physicochemical equipment; gaskets for analytical equipment and instruments; ferrules for analytical equipment and instruments; valve seats; U-cups; linings for chemical equipment, gasoline tanks, wind tunnels, etc., and corrosion-resistant linings for anodized tanks; coatings for masking jigs for plating; valve parts for analytical equipment and physicochemical equipment; expansion joints for flue gas desulfurization plants; acid-resistant hoses for concentrated sulfuric acid, chlorine gas transfer hoses, oil-resistant hoses, and rainwater drain hoses for benzene and toluene storage tanks; chemical-resistant tubes and medical tubes used in analytical equipment and physicochemical equipment; trichloroethylene-resistant rolls and dyeing rolls for textile dyeing; drug stoppers; medical rubber stoppers; drug solution bottles, drug solution tanks, bags, chemical containers; protective equipment such as strong acid-resistant and solvent-resistant gloves and boots.

In the photographic field, such as the developing machines mentioned above, the printing field, such as printing machines, and the painting field, such as painting equipment, they can be used as rolls, belts, seals, valve parts, etc. of dry copying machines.

Specific examples of use in the above-mentioned photographic, printing and coating fields include the surface layer of a transfer roll in a copying machine, a cleaning blade in a copying machine, and a belt in a copying machine; rolls (for example, fixing rolls, pressure rolls, etc.) and belts for office equipment such as copying machines, printers and facsimiles; rolls, roll blades and belts in PPC copying machines; rolls in film developing machines and X-ray film developing machines; printing rolls, scrapers, tubes, valve parts and belts in printing machines; ink tubes, rolls and belts in printers; coating rolls, scrapers, tubes and valve parts in coating and painting equipment; developing rolls, gravure rolls, guide rolls, guide rolls in magnetic tape manufacturing coating lines, gravure rolls and coating rolls in magnetic tape manufacturing coating lines, etc.

In the food equipment field, which includes the above food plant equipment and household goods, it can be used in food manufacturing processes, food transport devices, or food storage devices.

Specific examples of uses in the food equipment field include seals for plate-type heat exchangers, solenoid valve seals for vending machines, packing for jar pots, sanitary pipe packing, packing for pressure cookers, seals for water heaters, gaskets for heat exchangers, diaphragms and packing for food processing equipment, and rubber materials for food processing equipment (for example, heat exchanger gaskets, various seals such as diaphragms and O-rings, piping, hoses, sanitary packing, valve packing, and packing for filling used as a joint between the mouth of a bottle or the like and the filler during filling). Other examples include packing, gaskets, tubes, diaphragms, hoses, and joint sleeves used in products such as alcoholic beverages and soft drinks, filling equipment, food sterilization equipment, brewing equipment, water heaters, and various automatic food vending machines.

In the nuclear power plant equipment field, it can be used for check valves and pressure reducing valves around the reactor, and seals for uranium hexafluoride enrichment equipment.

Specific uses in the above general industrial fields include sealing materials for hydraulic equipment such as machine tools, construction machinery, and hydraulic machinery; seals and bearing seals for hydraulic and lubricating machines; sealing materials used in mandrels, etc.; seals used in windows of dry cleaning equipment; cyclotron seals and (vacuum) valve seals, proton accelerator seals, automatic packaging machine seals, pump diaphragms for airborne sulfur dioxide and chlorine gas analyzers (pollution measuring devices), snake pump linings, rolls and belts in printing presses, transport belts (conveyor belts), squeeze rolls for pickling iron plates, etc., robot cables, solvent squeeze rolls for aluminum rolling lines, O-rings for couplers, acid-resistant cushioning materials, dust seals and lip rubber for the sliding parts of cutting machines, gaskets for food waste incineration machines, friction materials, metal or rubber surface modifiers, coating materials, etc. It can also be used as a gasket or sealing material for equipment used in papermaking processes, a sealant for clean room filter units, a construction sealant, a protective coating for concrete and cement, a glass cloth impregnation material, a processing aid for polyolefins, an additive for improving the moldability of polyethylene, a fuel container for small generators and lawnmowers, and precoated metal obtained by applying a primer treatment to metal plates. It can also be used as a sheet or belt by impregnating woven fabric and baking it.

Specific examples of uses in the steel industry include steel processing rolls for steel processing equipment.

Specific examples of use in the electrical field include insulating oil caps for bullet trains, venting seals for liquid-sealed transformers, transformer seals, jackets for oil well cables, seals for ovens such as electric furnaces, window frame seals for microwave ovens, sealants used to bond the wedge and neck of a CRT, sealants for halogen lamps, fixing agents for electrical parts, sealants for the end treatment of sheathed heaters, and sealants used for insulating and moisture-proofing treatment of lead wire terminals for electrical equipment. It can also be used as a coating material for oil-resistant and heat-resistant electric wires, high heat-resistant electric wires, chemical-resistant electric wires, high insulation electric wires, high-voltage transmission lines, cables, electric wires used in geothermal power generation equipment, and electric wires used around automobile engines. It can also be used for oil seals and shaft seals for vehicle cables. It can also be used as an electrical insulating material (for example, materials used for insulating spacers for various electrical equipment, insulating tapes used in cable joints and ends, heat-shrinkable tubes, etc.) and electrical and electronic equipment materials used in high-temperature atmospheres (for example, lead wire materials for motors, electric wire materials around high-temperature furnaces). It can also be used in the sealing layer and protective film (back sheet) of solar cells.

In the fuel cell field, it can be used as a sealing material between electrodes and between electrodes and separators in solid polymer fuel cells, phosphate fuel cells, etc., as well as seals, packing, and separators for piping for hydrogen, oxygen, generated water, etc.

In the electronic components field, it can be used as a raw material for heat dissipation materials, electromagnetic wave shielding materials, gaskets for computer hard disk drives (magnetic recording devices), etc. It is also used as a shock absorber (crash stopper) for hard disk drives, a binder for electrode active materials in nickel-hydrogen secondary batteries, a binder for active materials in lithium-ion batteries, a polymer electrolyte for lithium secondary batteries, a binder for the positive electrode of alkaline storage batteries, a binder for EL elements (electroluminescence elements), a binder for electrode active materials in capacitors, a sealant, a sealing agent, a quartz coating material for optical fibers, a film or sheet such as an optical fiber coating material, CMOS electronic circuits, transistors, integrated circuits, organic transistors, light-emitting elements, actuators, memories, sensors, coils, capacitors, resistors, and other electronic components, potting, coatings, and adhesive seals for circuit boards, fixing agents for electronic components, sealant modifiers such as epoxy, coating agents for printed circuit boards, modified materials for printed wiring board prepreg resins such as epoxy, shatterproof materials for light bulbs, gaskets for computers, large computer cooling hoses, packing such as gaskets and O-rings for secondary batteries, especially for lithium secondary batteries, sealing layers covering one or both sides of the outer surface of organic EL structures, connectors, dampers, and the like.

In the field of chemical transport equipment, it can be used in safety valves and shipping valves for trucks, trailers, tank trucks, ships, etc.

In the field of oil, gas, and other energy resource exploration and mining equipment parts, they are used as various sealing materials used when mining for oil, natural gas, etc., and as boots for electrical connectors used in oil wells.

Specific uses in the above-mentioned energy resource exploration and mining equipment parts field include drill bit seals, pressure adjustment diaphragms, seals for horizontal drilling motors (stators), stator bearing (shaft) seals, sealing materials used in blowout preventers (BOPs), sealing materials used in rotary blowout preventers (pipe wipers), sealing materials and gas-liquid connectors used in MWDs (real-time drilling information detection systems), logging tool seals (e.g., O-rings, seals, packing, gas-liquid connectors, boots, etc.) used in logging equipment, expansion packers, completion packers and packer seals used therein, seals, packing, and perforators used in cementing equipment. Seals used in drilling equipment, seals, packings and motor linings used in mud pumps, underground audiometer covers, U-cups, composition seating cups, rotary seals, laminated elastomeric bearings, flow control seals, sand control seals, safety valve seals, seals for hydraulic fracturing equipment, seals and packings for linear packers and linear hangers, seals and packings for wellheads, seals and packings for chokes and valves, sealing materials for LWD (logging while drilling), diaphragms used in oil exploration and drilling applications (for example, diaphragms for supplying lubricating oil to oil drilling pits), gate valves, electronic boots, sealing elements for drilling guns, etc.

Other applications include sealing joints in kitchens, bathrooms, washrooms, etc.; covering cloths for outdoor tents; seals for printing materials; rubber hoses for gas heat pumps, fluorocarbon-resistant rubber hoses; agricultural films, linings, and weather-resistant covers; and laminated steel tanks used in the construction and home appliance fields.

Furthermore, it can also be used as an article bonded to a metal such as aluminum. Examples of such uses include door seals, gate valves, pendulum valves, solenoid tips, as well as piston seals and diaphragms bonded to metals, metal-rubber parts bonded to metals such as metal gaskets, etc.

It can also be used for rubber parts, brake shoes, brake pads, etc. on bicycles.

The molded products can also be used for belts.

Examples of belts include the following: power transmission belts (including flat belts, V-belts, V-ribbed belts, toothed belts, etc.); flat belts used as conveyor belts in various high-temperature locations such as around the engines of agricultural machinery, machine tools, industrial machinery, etc.; conveyor belts for transporting loose materials and granular materials such as coal, crushed stone, soil, ore, wood chips, etc. in high-temperature environments; conveyor belts used in steelworks such as blast furnaces; conveyor belts for applications exposed to high-temperature environments such as precision equipment assembly factories and food factories; V-belts and V-ribbed belts for agricultural machinery, general equipment (for example, office equipment, printing machines, commercial dryers, etc.), automobiles, etc.; transmission belts for transport robots; toothed belts such as transmission belts for food machinery and machine tools; toothed belts for automobiles, office equipment, medical use, printing machines, etc.

In particular, timing belts are a typical example of toothed belts for automobiles.

The belt may be of single layer or multi-layer construction.

When the belt has a multi-layer structure, it may be composed of a layer obtained by crosslinking a fluororubber crosslinking composition and a layer composed of another material.

In multi-layer belts, layers made of other materials include layers made of other rubbers, layers made of thermoplastic resins, various fiber reinforcement layers, canvas, metal foil layers, etc.

The molded products can also be used for industrial anti-vibration pads, anti-vibration mats, railway slab mats, pads, automotive anti-vibration rubber, etc. Examples of automotive anti-vibration rubber include anti-vibration rubber for engine mounts, motor mounts, member mounts, strut mounts, bushes, dampers, muffler hangers, and center bearings.

Other applications include joint components such as flexible joints and expansion joints, boots, grommets, etc. In the marine industry, examples include marine pumps, etc.

Joint materials are joints used in piping and piping equipment, and are used for purposes such as preventing vibrations and noise generated by piping systems, absorbing expansion and contraction and displacement caused by temperature and pressure changes, absorbing dimensional fluctuations, and mitigating and preventing the effects of earthquakes and land subsidence.

Flexible joints and expansion joints can be preferably used as complex shaped molded articles for, for example, shipbuilding piping, mechanical piping such as pumps and compressors, chemical plant piping, electrical piping, civil engineering and water piping, and automobiles.
The boots can be preferably used as complex shaped molded articles, for example, automobile boots such as constant velocity joint boots, dust covers, rack and pinion steering boots, pin boots, and piston boots, as well as various industrial boots such as boots for agricultural machinery, boots for industrial vehicles, boots for construction machinery, boots for hydraulic machinery, boots for pneumatic machinery, boots for centralized lubricators, boots for transferring liquids, boots for firefighting, and boots for transferring various liquefied gases.

The molded products can also be used as diaphragms for filter presses, blowers, water supply diaphragms, liquid storage tanks, pressure switches, accumulators, and air spring diaphragms for suspensions, etc.

By adding the molded product to rubber or resin, an anti-slip agent is obtained that produces molded products and coating films that are less slippery in wet environments such as rain, snow, ice, and sweat.

The molded products can also be used as cushioning materials for hot press molding when producing decorative plywood, printed circuit boards, electrical insulating boards, rigid polyvinyl chloride laminates, etc., using melamine resin, phenolic resin, epoxy resin, etc.

The molded articles can also contribute to impermeability of various substrates, such as weapon-related sealing gaskets and protective clothing against contact with aggressive chemical agents.

It can also be used in O-rings, V-rings, X-rings, packing, gaskets, diaphragms, oil seals, bearing seals, lip seals, plunger seals, door seals, lip and face seals, gas delivery plate seals, wafer support seals, barrel seals and other various sealing materials used to seal lubricating oils (engine oils, transmission oils, gear oils, etc.) containing amine additives (especially amine additives used as antioxidants and detergent dispersants) used in automobiles, ships and other transportation means, as well as in tubes, hoses, various rubber rolls, coatings, belts, valve bodies, etc. It can also be used as a laminating material and a lining material.

The material can be used as a coating material for heat- and oil-resistant electric wires used in lead wires of sensors that come into contact with transmission oil and/or engine oil in internal combustion engines of automobiles, etc. to detect the oil temperature and/or oil pressure, and can also be used in high-temperature oil environments such as in automatic transmissions and engine oil pans.

In addition, vulcanized coatings may be formed on molded products for use. Specific applications include non-adhesive oil-resistant rolls for copying machines, weather-resistant anti-icing weather strips, rubber stoppers for infusions, rubber vial stoppers, mold release agents, non-adhesive light-duty conveyor belts, anti-adhesive coatings for plate gaskets in automobile engine mounts, coatings for synthetic fibers, and bolt components or joints with a thin layer of packing coating.

Note that the use of molded products for automobile-related parts also includes use in motorcycle parts with similar structures.

Fuels used in the automobile industry include diesel, gasoline, and diesel engine fuel (including biodiesel fuel).

The molded products can also be used as sealing components for rolling bearings.

The above-mentioned rolling bearings include ball bearings, roller bearings, bearing units, linear bearings, etc.

Examples of ball bearings include radial ball bearings, thrust ball bearings, and thrust angular ball bearings.

Examples of the above radial ball bearings include deep groove ball bearings, angular contact ball bearings, four-point contact ball bearings, self-aligning ball bearings, etc.

The above deep groove ball bearings are used, for example, in electric motors, household electrical appliances, office equipment, etc.

The above angular contact ball bearings include single-row angular contact ball bearings, combined angular contact ball bearings, double-row angular contact ball bearings, etc. Single-row angular contact ball bearings are used in electric motors, household electrical appliances, office equipment, etc., as well as hydraulic pumps and vertical pumps that are subject to axial loads in addition to radial loads. Combined angular contact ball bearings are used in machine tool main shafts and grinding spindles, etc., where improved shaft rotation accuracy and increased rigidity are required. Double-row angular contact ball bearings are used in electromagnetic clutches for automobile air conditioners, etc.

The above four-point contact ball bearings are subjected to axial loads from both directions and are used in reducers and other devices where a large space cannot be provided for the bearing width.

The above self-aligning ball bearings are used in places where it is difficult to align the shaft with the housing, or on transmission shafts where the shaft is prone to bending.

The above thrust ball bearings include single-direction thrust ball bearings and double-direction thrust ball bearings, and are applicable to the conventionally known applications in which these ball bearings are used.

The above thrust angular ball bearings are used in combination with double-row cylindrical roller bearings to support the axial load of the main shafts of machine tools.

Examples of the roller bearings include radial roller bearings and thrust roller bearings.

Examples of the above radial roller bearings include cylindrical roller bearings, needle roller bearings, tapered roller bearings, and spherical roller bearings.

The above cylindrical roller bearings are used in general machinery, machine tools, electric motors, reducers, railway axles, aircraft, etc.

Needle roller bearings are used in general machinery, automobiles, electric motors, etc.

Tapered roller bearings are used in machine tools, automotive and railway axles, rolling mills, reducers, etc.

Spherical roller bearings are used in general machinery, rolling mills, paper-making machines, axles, etc.

Examples of the above thrust roller bearings include thrust cylindrical roller bearings, thrust needle roller bearings, thrust tapered roller bearings, and thrust spherical roller bearings.

Thrust cylindrical roller bearings are used in machine tools, general machinery, etc.

Thrust needle roller bearings are used in automobiles, pumps, general machinery, etc.

Thrust tapered roller bearings are used in general machinery, rolling mills, etc.

Self-aligning thrust roller bearings are used in cranes, extruders, general machinery, etc.

In addition to being used as a molded product after crosslinking, the fluororubber crosslinking composition can also be used as various parts in various industrial fields. Next, the uses of the fluororubber crosslinking composition will be explained.

Fluororubber crosslinking compositions can be used as surface modifiers for metals, rubber, plastics, glass, etc.; sealing and coating materials such as metal gaskets and oil seals that require heat resistance, chemical resistance, oil resistance, and non-stickiness; non-stick coating materials or bleed barriers for rolls for office equipment, belts for office equipment, etc.; and for impregnating woven fabric sheets and belts, or applying them by baking.

By making the fluororubber cross-linking composition high-viscosity and high-concentration, it can be used in the usual way as a sealing material, lining, or sealant with complex shapes, by making it low-viscosity, it can be used to form thin films of a few microns, and by making it medium-viscosity, it can be used to apply pre-coated metal, O-rings, diaphragms, and reed valves.

In addition, it can also be used to coat woven fabric or paper transport rolls or belts, printing belts, chemical-resistant tubes, chemical stoppers, fuel hoses, etc.

Examples of substrates that can be coated with the fluororubber cross-linking composition include metals such as iron, stainless steel, copper, aluminum, and brass; glass products such as glass plates and woven and nonwoven glass fiber fabrics; molded products and coatings made from general-purpose and heat-resistant resins such as polypropylene, polyoxymethylene, polyimide, polyamideimide, polysulfone, polyethersulfone, and polyetheretherketone; molded products and coatings made from general-purpose rubbers such as SBR, butyl rubber, NBR, and EPDM, and heat-resistant rubbers such as silicone rubber and fluororubber; woven and nonwoven fabrics made from natural and synthetic fibers; and the like.

Coatings formed from the fluororubber crosslinking composition can be used in fields requiring heat resistance, solvent resistance, lubricity, and non-stickiness. Specific applications include rolls (e.g., fixing rolls, pressure rolls) and conveyor belts for office automation equipment such as copiers, printers, and facsimiles; sheets and belts; O-rings, diaphragms, chemical-resistant tubes, fuel hoses, valve seals, gaskets for chemical plants, and engine gaskets.

The fluororubber crosslinking composition can also be dissolved in a solvent and used as a paint or adhesive. It can also be used as a paint in the form of an emulsion dispersion (latex).

Fluororubber cross-linking compositions are used as sealing materials and linings for various devices and pipes, etc., and as surface treatment agents for structures made of inorganic and organic substrates such as metals, ceramics, glass, stone, concrete, plastics, rubber, wood, paper, and textiles.

The fluororubber cross-linking composition can be applied to a substrate, etc., by dispenser coating or screen printing coating.

The fluororubber crosslinking composition may be used as a coating composition for casting films or for dipping substrates such as fabrics, plastics, metals, or elastomers.

In particular, the fluororubber crosslinking composition, in the form of a latex, may be used to produce coated fabrics, protective gloves, impregnated fibers, O-ring coatings, coatings for fuel system quick connect O-rings, coatings for fuel system seals, coatings for fuel tank rollover valve diaphragms, coatings for fuel tank pressure sensor diaphragms, coatings for oil filters and fuel filter seals, coatings for fuel tank sender seals and sender head fitting seals, coatings for copier fuser rolls, and polymer coating compositions.

They are useful for coating silicone rubber, nitrile rubber, and other elastomers. They are also useful for coating parts made from such elastomers for the purpose of enhancing both the permeation and chemical resistance of the substrate elastomer as well as its thermal stability. Other applications include coatings for heat exchangers, expansion joints, vats, tanks, fans, flue ducts and other ductwork, and containment structures, such as concrete containment structures. The fluoroelastomer crosslinking composition may be applied to exposed cross sections of multi-layer component structures, such as in hose construction and diaphragm manufacturing methods. Sealing members at connections and joints are often made of hard materials, and the fluoroelastomer crosslinking composition provides improved frictional interfaces, enhanced dimensional interference fits with reduced trace leakage along the sealing surfaces. The latex enhances seal durability in various automotive system applications.

They can also be used in the manufacture of power steering systems, fuel systems, air conditioning systems, and any joints where hoses and tubes are connected to another component. A further utility of the fluororubber crosslinking composition is in repairing manufacturing defects (and damage due to use) in multi-layer rubber structures such as three-layer fuel hoses. The fluororubber crosslinking composition is also useful in coating thin steel sheets, which may be formed or embossed before or after paint is applied. For example, multiple layers of coated steel can be assembled to make a gasket between two rigid metal members. The sealing effect is obtained by applying the fluororubber crosslinking composition between the layers. This process can be used to manufacture engine head gaskets and exhaust manifold gaskets for the purpose of lowering the bolt forces and strains of the assembled parts while providing good fuel economy and low emissions due to low cracks, deflections, and hole strains.

The fluororubber cross-linking composition can also be used as a coating agent; a substrate-integrated gasket or packing formed by dispenser molding on a substrate containing inorganic materials such as metals or ceramics; or a multi-layered product formed by coating a substrate containing inorganic materials such as metals or ceramics.

The fluororubber crosslinking composition is also suitable as a wiring material for light and flexible electronic devices, and can be used in known electronic components. Examples of electronic components include CMOS electronic circuits, transistors, integrated circuits, organic transistors, light-emitting elements, actuators, memories, sensors, coils, capacitors, and resistors. By using this, flexible electronic devices such as solar cells, various displays, sensors, actuators, electronic artificial skin, sheet-type scanners, Braille displays, and wireless power transmission sheets can be obtained.

Although the embodiments have been described above, it will be understood that various changes in form and details are possible without departing from the spirit and scope of the claims.

（式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基、Ｘは、ビニル基、アリル基またはビニルオキシ基、Ｙは、Ｈ、または、Ｈａｍｍｅｔｔの置換基定数σｍおよびσｐの少なくとも一方の値が、０．０３以上である置換基（γ）（ただしヒドロキシ基を含有する置換基およびアルキルカルボニルオキシ基を除く）である）

（式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基、Ｘは、ビニル基、アリル基またはビニルオキシ基、ＹおよびＺは、それぞれ独立して、Ｈ、または、Ｈａｍｍｅｔｔの置換基定数σｍおよびσｐの少なくとも一方の値が、０．０３以上である置換基（γ）（ただしヒドロキシ基を含有する置換基およびアルキルカルボニルオキシ基を除く）である）

（式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基、Ｘは、ビニル基、アリル基またはビニルオキシ基、ＹおよびＺは、それぞれ独立して、Ｈ、または、Ｈａｍｍｅｔｔの置換基定数σｍおよびσｐの少なくとも一方の値が、０．０３以上である置換基（γ）（ただしヒドロキシ基を含有する置換基およびアルキルカルボニルオキシ基を除く）、Ａは、結合手、炭素数１～１３のアルキレン基、炭素数６～１３のアリーレン基、チオカルボニル基、酸素原子、カルボニル基、スルフィニル基またはスルホニル基、Ａのアルキレン基およびアリーレン基は、炭素原子に結合した水素原子の一部または全部が塩素原子またはフッ素原子により置換されていてもよい、環Ｂおよび環Ｃは、それぞれ独立して、単環または多環の芳香族環である）
＜３＞ 本開示の第３の観点によれば、
フッ素ゴム（ａ）、架橋剤（ｂ）、脱フッ化水素剤（ｃ）、および、有機パーオキサイド（ｄ）を含有し、架橋剤（ｂ）が、式（ｂ４）～（ｂ７）で示される化合物からなる群より選択される少なくとも１種であるフッ素ゴム架橋用組成物が提供される。

（各式中、Ｒは、水素原子、炭素数１～５のアルキル基または炭素数１～５のフッ素化アルキル基である）
＜４＞ 本開示の第４の観点によれば、
架橋剤（ｂ）が、式（ｂ５）および式（ｂ６）で示される化合物からなる群より選択される少なくとも１種である第３の観点によるフッ素ゴム架橋用組成物が提供される。
＜５＞ 本開示の第５の観点によれば、
フッ素ゴム（ａ）が、ビニリデンフルオライド単位を含む第１～第４のいずれかの観点によるフッ素ゴム架橋用組成物が提供される。
＜６＞ 本開示の第６の観点によれば、
架橋剤（ｂ）の含有量が、フッ素ゴム（ａ）１００質量部に対し、０．１～１０質量部である第１～第５のいずれかの観点によるフッ素ゴム架橋用組成物が提供される。
＜７＞ 本開示の第７の観点によれば、
有機パーオキサイド（ｄ）の含有量が、フッ素ゴム（ａ）１００質量部に対し、０．０５～１０質量部である第１～第６のいずれかの観点によるフッ素ゴム架橋用組成物が提供される。
＜８＞ 本開示の第８の観点によれば、
受酸剤（ｅ）をさらに含有し、受酸剤（ｅ）の含有量が、フッ素ゴム（ａ）１００質量部に対し、０．１～５０質量部である第１～第７のいずれかの観点によるフッ素ゴム架橋用組成物が提供される。
＜９＞ 本開示の第９の観点によれば、
第１～第８のいずれかの観点によるフッ素ゴム架橋用組成物から得られる成形品が提供される。 <1> According to a first aspect of the present disclosure,
The composition contains a fluororubber (a), a crosslinking agent (b), a dehydrofluorination agent (c), and an organic peroxide (d),
The crosslinking agent (b) is
1) at least one aromatic ring;
2) a group having a carbon-carbon double bond (excluding those constituting the aromatic ring), and
3) There is provided a composition for crosslinking fluororubber, which is a compound having, in the molecule, an alkylcarbonyloxy group directly bonded to a carbon atom constituting the aromatic ring.
<2> According to a second aspect of the present disclosure,
There is provided a composition for crosslinking fluororubber according to a first aspect, in which the crosslinking agent (b) is at least one selected from the group consisting of compounds represented by general formulas (b1) to (b3).

(In the formula, R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms; X is a vinyl group, an allyl group, or a vinyloxy group; Y is H, or a substituent (γ) having at least one of the Hammett substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxy group and alkylcarbonyloxy groups).)

(In the formula, R represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms; X represents a vinyl group, an allyl group, or a vinyloxy group; Y and Z each independently represent H or a substituent (γ) having at least one of the Hammett substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxy group and alkylcarbonyloxy groups).

(wherein R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms or a fluorinated alkyl group having 1 to 5 carbon atoms; X is a vinyl group, an allyl group or a vinyloxy group; Y and Z are each independently H or a substituent (γ) having at least one value of Hammett's substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxyl group and alkylcarbonyloxy groups); A is a bond, an alkylene group having 1 to 13 carbon atoms, an arylene group having 6 to 13 carbon atoms, a thiocarbonyl group, an oxygen atom, a carbonyl group, a sulfinyl group or a sulfonyl group; in the alkylene group and arylene group of A, some or all of the hydrogen atoms bonded to carbon atoms may be substituted with chlorine atoms or fluorine atoms; and ring B and ring C are each independently a monocyclic or polycyclic aromatic ring.)
<3> According to a third aspect of the present disclosure,
The present invention provides a composition for crosslinking a fluororubber, comprising a fluororubber (a), a crosslinking agent (b), a dehydrofluorination agent (c), and an organic peroxide (d), in which the crosslinking agent (b) is at least one selected from the group consisting of compounds represented by the formulas (b4) to (b7).

(In each formula, R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms.)
<4> According to a fourth aspect of the present disclosure,
There is provided a composition for crosslinking fluororubber according to a third aspect, in which the crosslinking agent (b) is at least one selected from the group consisting of compounds represented by formula (b5) and formula (b6).
<5> According to a fifth aspect of the present disclosure,
There is provided a composition for crosslinking fluororubber according to any one of the first to fourth aspects, in which the fluororubber (a) contains vinylidene fluoride units.
<6> According to a sixth aspect of the present disclosure,
There is provided a composition for crosslinking fluororubber according to any one of the first to fifth aspects, in which the content of the crosslinking agent (b) is 0.1 to 10 parts by mass per 100 parts by mass of the fluororubber (a).
<7> According to a seventh aspect of the present disclosure,
There is provided a composition for crosslinking a fluororubber according to any one of the first to sixth aspects, in which the content of the organic peroxide (d) is 0.05 to 10 parts by mass per 100 parts by mass of the fluororubber (a).
<8> According to an eighth aspect of the present disclosure,
There is provided a composition for crosslinking a fluororubber according to any of the first to seventh aspects, further comprising an acid acceptor (e), the content of the acid acceptor (e) being 0.1 to 50 parts by mass per 100 parts by mass of the fluororubber (a).
<9> According to a ninth aspect of the present disclosure,
There is provided a molded article obtained from the fluororubber crosslinking composition according to any one of the first to eighth aspects.

Next, we will explain the embodiments of the present disclosure by giving examples, but the present disclosure is not limited to these examples.

The values in the examples were measured using the following methods.

<Monomer composition of fluororubber>
The measurements were carried out using a ¹⁹ F-NMR (AC300P model, manufactured by Bruker).

<Fluorine content>
The content was calculated from the composition of the fluororubber measured by ¹⁹ F-NMR.

<Mooney Viscosity>
Measurement was performed in accordance with ASTM D1646-15 and JIS K6300-1:2013. The measurement temperature was 100°C.

<Glass transition temperature (Tg)>
A DSC curve was obtained by heating 10 mg of a sample at 20° C./min using a differential scanning calorimeter (DSC822e, manufactured by Mettler Toledo, or X-DSC7000, manufactured by Hitachi High-Tech Science). The glass transition temperature was determined as the temperature indicating the intersection point between an extension of the baseline before and after the secondary transition of the DSC curve and a tangent to the inflection point of the DSC curve.

<Heat of fusion>
A differential scanning calorimeter (DSC822e, manufactured by Mettler Toledo, or X-DSC7000, manufactured by Hitachi High-Tech Science) was used to obtain a DSC curve by heating 10 mg of a sample at a rate of 20° C./min, and the heat of fusion was calculated from the magnitude of the melting peak (ΔH) that appeared in the DSC curve.

<Iodine content>
An absorbing solution was prepared by mixing _Na2CO3 and _K2CO3 in a 1:1 ratio (by weight) and dissolving _the resulting mixture in 20 _ml of pure water. A mixture was prepared by mixing 12 mg of a sample ( _fluororubber ) with 5 mg of _Na2SO3 , and burning the mixture in oxygen in a quartz flask, and introducing the generated combustion gas into the absorbing solution. The resulting absorbing solution was left for 30 minutes, and then the concentration of iodine ions in the absorbing solution was measured using a Shimadzu 20A ion chromatograph. The content of iodine ions was determined using a calibration curve prepared using a KI standard solution containing 0.5 ppm iodine ions and a KI standard solution containing 1.0 ppm iodine ions.

<Cross-linking characteristics (maximum torque (MH), optimal cross-linking time (T90))>
For the fluororubber crosslinking composition, a vulcanization tester (MDR H2030 manufactured by M&K Co., Ltd.) was used during primary crosslinking to obtain crosslinking curves at the temperatures listed in each table, and the maximum torque (MH) and optimal crosslinking time (T90) were obtained from the change in torque. A higher maximum torque (MH) means a higher crosslink density.

<Tensile strength and elongation at break>
A test piece in the shape of a dumbbell No. 6 was prepared using a crosslinked sheet having a thickness of 2 mm. Using the obtained test piece and a tensile tester (Tensilon RTG-1310 manufactured by A&D Co., Ltd.), the tensile strength and elongation at break were measured at 23°C under the condition of 500 mm/min in accordance with JIS K6251:2010.

<Hardness>
Three crosslinked sheets having a thickness of 2 mm were stacked, and the durometer hardness (type A, peak value) was measured in accordance with JIS K6251-3:2012.

<Compression set>
Using a small test piece for measuring compression set, the measurement was performed in accordance with JIS K6262:2013, Method A, at a compression ratio of 25%, a test temperature of 200°C, and a test time of 72 hours.

In the examples and comparative examples, the following materials were used.
Fluorine rubber A:
Vinylidene fluoride/hexafluoropropylene molar ratio: 78/22
Fluorine content: 66%
Mooney viscosity (ML1+10 (100°C)): 60
Glass transition temperature: -18°C
Heat of fusion: None observed in the second run Iodine content: 0.17% by mass
Fluorine Rubber B
Vinylidene fluoride/hexafluoropropylene molar ratio: 78/22
Fluorine content: 66%
Mooney viscosity (ML1+10 (100°C)): 70
Glass transition temperature: -18°C
Heat of fusion: Not observed in the second run Does not contain iodine atoms

MT Carbon ( _N2SA : ^8m2 /g, DBP: 43ml/100g)
Crosslinker A: 4-vinylphenyl acetate Crosslinker B: 4-allylphenol Crosslinker C: eugenol Dehydrofluorination agent A: A mixture of 91% by weight of benzyldimethyloctadecylammonium chloride and 9% by weight of isopropyl alcohol Organic peroxide A: 2,5-dimethyl-2,5-bis(t-butylperoxy)hexane Calcium hydroxide Magnesium oxide

Example 1
100 parts by mass of fluororubber A, 20 parts by mass of MT carbon, 4 parts by mass of crosslinking agent A, 0.7 parts by mass of dehydrofluorination agent A, 0.5 parts by mass of organic peroxide A, 6 parts by mass of calcium hydroxide, and 3 parts by mass of magnesium oxide were blended and kneaded on an open roll to prepare a fluororubber crosslinking composition. The maximum torque (MH) and optimal crosslinking time (T90) of the obtained fluororubber crosslinking composition are shown in Table 1. Next, the fluororubber crosslinking composition was crosslinked by primary crosslinking (press crosslinking) under the conditions shown in Table 1 and secondary crosslinking (oven crosslinking) under the conditions shown in Table 1 to obtain a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set. The evaluation results of the obtained crosslinked sheet and the results of the compression set test are shown in Table 1.

Example 2
A fluororubber crosslinking composition was prepared in the same manner as in Example 1, except that the crosslinking agent A was changed to the crosslinking agent B, and a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set were obtained. The results are shown in Table 1.

Comparative Example 1
A fluororubber crosslinking composition was prepared in the same manner as in Example 1, except that the crosslinking agent A was changed to the crosslinking agent C, and a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set were obtained. The results are shown in Table 1.

Example 3
A fluororubber crosslinking composition was prepared in the same manner as in Example 1, except that the amount of crosslinking agent A was changed to 2 parts by mass, and a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set were obtained. The results are shown in Table 1.

Comparative Example 2
A fluororubber crosslinking composition was prepared in the same manner as in Comparative Example 1, except that the amount of crosslinking agent C was changed to 2 parts by mass, and a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set were obtained. The results are shown in Table 1.

Comparative Example 3
A fluororubber cross-linking composition was prepared in the same manner as in Example 1, except that no cross-linking agent A was added. The results are shown in Table 1.

Example 4
100 parts by mass of fluororubber B, 20 parts by mass of MT carbon, 4 parts by mass of crosslinking agent A, 0.7 parts by mass of dehydrofluorination agent A, 0.5 parts by mass of organic peroxide A, 6 parts by mass of calcium hydroxide, and 3 parts by mass of magnesium oxide were blended and kneaded on an open roll to prepare a fluororubber crosslinking composition. The maximum torque (MH) and optimal crosslinking time (T90) of the obtained fluororubber crosslinking composition are shown in Table 2. Next, the fluororubber crosslinking composition was crosslinked by primary crosslinking (press crosslinking) under the conditions shown in Table 2 and secondary crosslinking (oven crosslinking) under the conditions shown in Table 2 to obtain a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set. The evaluation results of the obtained crosslinked sheet and the results of the compression set test are shown in Table 2.

Comparative Example 4
A fluororubber crosslinking composition was prepared in the same manner as in Example 4, except that the crosslinking agent A was changed to the crosslinking agent C, and a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set were obtained. The results are shown in Table 2.

Example 5
A fluororubber crosslinking composition was prepared in the same manner as in Example 4, except that the amount of crosslinking agent A was changed to 2 parts by mass, and a crosslinked sheet (thickness 2 mm) and a small test piece for measuring compression set were obtained. The results are shown in Table 2.

Claims (9)

The composition contains a fluororubber (a), a crosslinking agent (b), a dehydrofluorination agent (c), and an organic peroxide (d),
The crosslinking agent (b) is
1) at least one aromatic ring;
2) a group having a carbon-carbon double bond (excluding those constituting the aromatic ring), and
3) A composition for crosslinking fluororubber, which is a compound having, in the molecule, an alkylcarbonyloxy group directly bonded to a carbon atom constituting the aromatic ring. The fluororubber crosslinking composition according to claim 1, wherein the crosslinking agent (b) is at least one selected from the group consisting of compounds represented by general formulas (b1) to (b3):

(In the formula, R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms; X is a vinyl group, an allyl group, or a vinyloxy group; Y is H, or a substituent (γ) having at least one of the Hammett substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxy group and alkylcarbonyloxy groups).)

(In the formula, R represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms; X represents a vinyl group, an allyl group, or a vinyloxy group; Y and Z each independently represent H or a substituent (γ) having at least one of the Hammett substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxy group and alkylcarbonyloxy groups).

(wherein R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms or a fluorinated alkyl group having 1 to 5 carbon atoms; X is a vinyl group, an allyl group or a vinyloxy group; Y and Z are each independently H or a substituent (γ) having at least one value of Hammett's substituent constants σm and σp of 0.03 or more (excluding substituents containing a hydroxyl group and alkylcarbonyloxy groups); A is a bond, an alkylene group having 1 to 13 carbon atoms, an arylene group having 6 to 13 carbon atoms, a thiocarbonyl group, an oxygen atom, a carbonyl group, a sulfinyl group or a sulfonyl group; in the alkylene group and arylene group of A, some or all of the hydrogen atoms bonded to carbon atoms may be substituted with chlorine atoms or fluorine atoms; and ring B and ring C are each independently a monocyclic or polycyclic aromatic ring.) A composition for crosslinking a fluororubber, comprising a fluororubber (a), a crosslinking agent (b), a dehydrofluorination agent (c), and an organic peroxide (d), wherein the crosslinking agent (b) is at least one selected from the group consisting of compounds represented by formulas (b4) to (b7).

(In each formula, R is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a fluorinated alkyl group having 1 to 5 carbon atoms.) The fluororubber crosslinking composition according to claim 3, wherein the crosslinking agent (b) is at least one selected from the group consisting of compounds represented by formula (b5) and formula (b6). The fluororubber crosslinking composition according to any one of claims 1 to 4, wherein the fluororubber (a) contains vinylidene fluoride units. The fluororubber cross-linking composition according to any one of claims 1 to 4, wherein the content of the cross-linking agent (b) is 0.1 to 10 parts by mass per 100 parts by mass of the fluororubber (a). The fluororubber cross-linking composition according to any one of claims 1 to 4, wherein the content of the organic peroxide (d) is 0.05 to 10 parts by mass per 100 parts by mass of the fluororubber (a). The fluororubber crosslinking composition according to any one of claims 1 to 4, further comprising an acid acceptor (e), the content of the acid acceptor (e) being 0.1 to 50 parts by mass per 100 parts by mass of the fluororubber (a). A molded article obtained from the fluororubber crosslinking composition according to any one of claims 1 to 4.