JPH06329818A - Bonding of fluororesin material - Google Patents

Abstract

PURPOSE:To bond a fluororesin material to the same or different material in extremely high bonding strength without deteriorating the properties of the resin by contacting a fluororesin material with a specific solution and irradiating the interface with ultraviolet ray. CONSTITUTION:A fluororesin material is made to contact with a solution containing a compound having an atom with a bond energy of >=128Kcal/mol to fluorine atom and having a hydrophilic group, lipophilic group or a characteristic functional group of an adhesive and irradiated with ultraviolet ray having a photon energy of >=128Kcal while keeping the contacting state to effect the surface-modification treatment by the defluorination simultaneously with the substitution with a functional group having affinity to an adhesive. The treated material is bonded to the same or different material with an adhesive. A compound of boron, aluminum, barium, gallium, lithium, hydrogen or titanium such as (BHNH)3, AlCl3 and Ba(OH)2 is used as the compound used as the solute of the solution. The irradiation with photon energy is carried out by using an ArF excimer laser and deforming the laser beam to a linear form with a cylindrical lens. As an alternative, a Hg lamp, etc., may be used as the ultraviolet source.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for adhering fluororesin materials to each other or to fluororesin materials and different materials, a method for producing a fluororesin composite and a method for marking fluororesin materials.

[0002]

2. Description of the Related Art Since a fluororesin has a low affinity with other substances and is difficult to be adhered, conventionally, when adhering fluororesin materials to each other or fluororesin materials and dissimilar materials, the surface of the fluororesin material is It has been performed in advance to improve the adhesiveness by surface-treating it by some method. For example, liquid ammonia containing metallic sodium or a method of chemically modifying the surface of a fluororesin material with a treatment liquid containing naphthalene and tetrahydrofuran, sputtering,
Conventionally known is a method of physically modifying the surface of a fluororesin material by corona discharge, plasma or the like.

[0003]

However, in the conventional chemical modification method, there arises a problem that the surface of the fluororesin material becomes brown, the surface portion becomes brittle, and the adhesive layer peels off. On the other hand, also in the conventional physical surface modification method, the formed rough surface serves as a stress concentration point and induces a junction failure.
Therefore, high adhesive strength could not be obtained by any of the conventional methods.

Therefore, it is an object of the present invention to provide a method for adhering a fluororesin material which can obtain an extremely high adhesive strength. A further object of the present invention is to provide a method for producing a fluororesin material composite bonded with high adhesive strength. Another object of the present invention is to provide a method for marking a fluororesin material that is difficult to peel off.

[0005]

Means for Solving the Problems In order to solve the above problems, the present inventor has found that the binding energy with a fluorine atom is 128 Kc, which is the binding energy between a carbon atom and a fluorine atom.
atoms larger than al / mol, such as B, Al, Ba,
A solution having Ga, Li, H, and Ti and a functional group having an affinity for the adhesive, for example, —OH, —Cl, —NO ₂ or the like is brought into contact with the surface of the fluororesin material, and in that state, the fluororesin material Energy of 128K at the interface between
Irradiation with ultraviolet rays equal to or more than cal is used to defluorine the fluororesin material, and at the same time, the functional group is substituted,
A method of performing surface modification treatment and then joining it to another material via an adhesive was adopted.

That is, according to the present invention, the bonding energy with the fluorine atom is 128 Kcal prior to joining the fluororesin material with the same or different material through the adhesive.
/ Mol or more and a solution containing a compound having a hydrophilic group, a lipophilic group or a functional group specific to the adhesive, and the fluororesin material is brought into contact with the solution, and the interface between the fluororesin material and the solution in that state Is irradiated with ultraviolet rays having a photon energy of 128 Kcal or more, thereby defluorinating the fluororesin material, and at the same time, performing a surface modification treatment for substituting with a functional group having an affinity for the adhesive. A method of adhering materials is provided.

Further, the present invention provides an organic solvent in which the fluororesin materials surface-modified as described above or the surface-modified fluororesin material and the different type resin material are soluble in these The present invention provides a method for producing a fluororesin composite material, which is characterized by performing pressure-bonding bonding with.

Furthermore, the present invention provides a fluororesin ink or paint containing a compound having an atom having a binding energy with a fluorine atom of 128 Kcal / mol or more and a hydrophilic group, a lipophilic group or a functional group specific to the adhesive. The present invention provides a marking method for a fluororesin material, which comprises coating the material and irradiating the interface with ultraviolet rays having a photon energy of 128 Kcal or more.

In the present invention, the fluororesin means
A resin comprising a polymer or copolymer of a monomer containing a fluorine atom, and a resin having this as a base material,
Examples thereof include polytetrafluoroethylene, polytrifluoroethylene chloride, tetrafluoroethylene-hexafluoropropylene, and polyvinylidene fluoride.

The binding energy with the fluorine atom is 128K
Examples of compounds having cal / mol or more atoms include boron compounds, aluminum compounds, barium compounds, gallium compounds, lithium compounds, hydrogen compounds, and titanium compounds. Specifically, (BH
_{NH) 3, LiBH 4, NaBH} 4, KBH 4, CsB
_{H 4, H 3 BO 3,} B (CH 3) 3, B (C 2 H 5)
₃ , B (C ₃ H ₇ ) ₃ , B (C ₄ H ₉ ) ₃ , B (C ₆ H
₅ ) ₃ , B (OH) ₂ (C ₆ H ₅ ), NaB (C ₆ H
₅ ) ₄ , B (CH ₃ O) ₃ , B (C ₂ H ₅ O) ₃ , B
(C ₄ H ₉ O) ₃ , (NH ₄ ) ₂ B ₄ O ₇ , Al (O
H) ₃ , Al (NO ₃ ) ₃ , AlCl ₃ , AlBr ₃ ,
AlI ₃ , Al ₂ (SO ₄ ) ₃ , Al (CH ₃ COO)
₂ OH, Al ₂ BaO ₄ , NH ₄ AlCl ₄ , LiAl
H ₄ , AlNa (SO ₄ ) ₂ , AlK (SO ₄ ) ₂ , A
l (NH ₄ ) SO ₄ , Al (CH ₃ ) ₃ , Al (C ₃ H
₇ ) ₃ , Al (C ₂ H ₅ ) ₃ , Al (C ₆ H ₅ ) ₃ , A
l (C ₂ H ₅ O) ₃ , Al (C ₃ H ₇ O) ₃ , Al (C ₄
H ₉ O) ₃ , Ba (ClO ₄ ) ₂ , BaBr, BaI ₂
, Ba (OH) ₂ , BaS ₂ O ₃ , Ba (NO ₂ )
₂ , Ba (CN) ₂ , GaCl ₃ , GaBr, Ga (O
H) ₃ , Ga (SO ₄ ) ₃ , Ga (NO ₃ ) ₃ , Ga
(CH ₃ COO) ₃ , GaK (SO ₄ ) ₂ , Ga (CH
₃ ) ₃ , Ga (C ₂ H ₅ ) ₃ , Ga (C ₃ H ₇ ) ₃ , G
a (C ₄ H ₉ ) ₃ , Ga (C ₆ H ₅ ) ₃ , LiCl, L
iBr, LiI, LiOH, LiSH, LiN, LiN
O ₃ , Li (CH ₃ ), Li (hydrocarbon compound), Li
(C ₆ H ₅ ), LiCH ₃ O, LiAlH [OC (CH
₃ ) ₃ ] ₃ , LiNH ₂ , H ₂ O, D ₂ O, H ₂ O ₂ ,
HCOOH, CH ₃ COOH, HCl, HNO ₃ , H ₂
SO ₄ , C ₆ H ₆ , C ₆ H ₅ CH ₃ , Ti (CH ₂ C ₆
H ₅ ) ₄ , [Ti (C ₆ H ₅ ) ₂ ] ₂ , TiCl ₃ , T
mention may be made of iBr _4, TiI _4.

Examples of the functional group having an affinity with the adhesive include -OH, -Cl, -NO ₂ , -CN, -NH ₂ ,-.
_{COOH, -CO, -OCH 3, -OC} 2 H 5, -OC
_{3 H 7, -OC 4 H 9} , -CONH, -CH 3, -C 2
_{H 5, -CH 2, -SO 3} H, -C 3 H 7, -C 4 H
_9, can be exemplified -C ₆ H _5.

When the boron compound, the aluminum compound, the barium compound, the gallium compound and the lithium compound are liquid at room temperature, the interface with the sample may be irradiated with ultraviolet light having a photon energy of 128 Kcal or more in the liquid. When these compounds are solid or powder, water, heavy water, ammonia, sulfuric acid, carbon tetrachloride, hydrogen disulfide, hydrocarbons, halogen compounds, alcohols, phenols, organic acids and their derivatives, It may be dissolved in a solvent such as nitriles, nitro compounds, amines and sulfur compounds, and in the solution, ultraviolet rays having a photon energy of 128 Kcal or more may be applied to the interface with the sample.

Examples of the ultraviolet rays having a photon energy of 128 Kcal or more include those from ArF excimer laser, Hg lamp or Hg-Xe lamp. The ArF excimer laser may be transformed into a linear beam by a cylindrical lens and irradiated along the interface of the fluororesin material continuously pulled up from the solution with the solution. Further, ArF excimer laser may be irradiated through a pattern corresponding to the adhesive portion of the fluororesin material. Other examples of the above-mentioned ultraviolet rays may be from an ultraviolet lamp obtained by arc, corona or silent discharge in air, nitrogen or other gas atmosphere.

The binding energy with the fluorine atom is 128K
A solution containing a compound having a cal / mol or more atom and a hydrophilic group, a lipophilic group or a functional group specific to the adhesive is
It may be mixed in the adhesive in advance. Further, the mixed solution may be applied to the surface of the fluororesin material, and then the coating layer interface may be irradiated with ultraviolet rays having a photon energy of 128 Kcal or more to form an adhesive layer on the surface of the fluororesin material. . Further, a porous material is impregnated with a solution containing a compound having an atom having a binding energy with a fluorine atom of 128 Kcal / mol or more and a hydrophilic group, a lipophilic group or a functional group specific to the adhesive. In the state of being in close contact with the material, the photon energy at the interface is 1
You may irradiate with ultraviolet rays of 28 Kcal or more.

[0015]

As described above, in the present invention, defluorination is performed from the surface portion of the fluororesin material, and a functional group having an affinity for the adhesive is substituted in place of this fluorine, and as a result, the surface of the fluororesin material is replaced. Has improved affinity with the adhesive and achieves strong adhesive strength.

[0016]

The present invention will be described more specifically below with reference to the illustrated embodiments. (Example 1) The surface treatment of a fluororesin material (polytetrafluoroethylene) was performed using the apparatus shown in FIG. In addition,
In the figure, 1 is an excimer laser device, 2 is a mask, 3 is a mirror, 4 and 5 are lenses, 6 is a reaction container, and 7 is a fluororesin sheet as a sample.

First, methyl alcohol (C
H ₃ OH) 50 cc and a solution of 5 g of sodium tetrahydroborate (Na [BH ₄ ]) are filled, the fluororesin sheet 7 is put in the solution, and the interface between the solution and the fluororesin sheet 7 is irradiated with ArF laser light. As a result, both a lipophilic group and a hydrophilic group were expressed as shown in FIG. As a result of the infrared absorption spectrum measurement by ATR-FTIR, this was due to absorption at around 2900 cm ⁻¹ for the substitution of the methyl group, and 330 for the substitution of the hydroxyl group.
It was confirmed by absorption near 0 cm ^-1 . Defluorination was confirmed by X-ray photoelectron spectroscopy (XPS). The fluororesin sheet 7 thus treated was adhered to a stainless steel plate with an epoxy resin adhesive and a tensile shear test was conducted. As a result, an adhesive strength of 140 Kgf / cm ² was confirmed.

(Example 2) A fluororesin material (FEP) was surface-treated using the apparatus shown in FIG. In the figure, 1 is an excimer laser device, 2 is a mask, 3 is a mirror, 4 is a lens, 5 is a compound liquid, 6 is a reaction container, 7 is a fluororesin sheet as a sample, and 8 is a sponge sheet.

First, 5 g of sodium tetrahydroborate is dissolved in 50 cc of water, and this solution 5 is dipped in a sponge sheet 8 to suppress the generation of bubbles and the separation of the liquid from the fluororesin sheet sample 7, and then When a transparent fluororesin (FEP) sheet sample 7 was placed and irradiated with ArF laser light (10 mJ / cm ² ) from above, the contact angle with water was 110 degrees when untreated as shown in FIG. The thing was modified to 10 degrees. When this surface-modified fluororesin sheet sample was adhered to a stainless steel plate via Aron Alpha (trademark), 60 Kgf / cm ²
The adhesive strength of was confirmed.

Example 3 2 g of boric acid (H ₃ BO ₃ ) was dissolved in 50 cc of water, this solution was dipped in a sponge sheet, and a transparent fluororesin (FEP) sheet sample was treated in the same manner as in Example 2. When the ArF laser energy density was 15 mJ / cm ² , the hydroxyl group (OH) was substituted on the surface of the fluororesin sheet sample, and the contact angle with water became 5 degrees. When this surface-modified fluororesin sheet sample was adhered to a stainless plate via Aron Alpha (trademark), an adhesion strength of 60 Kgf / cm ² was confirmed.

(Example 4) 2 g of boric acid (H ₃ BO ₃ ) was dissolved in 50 cc of ammonia water, this solution was dipped in a sponge sheet, and a transparent fluororesin (FEP) sheet sample was prepared in the same manner as in Example 2. was treated, fluororesin sheet sample surface into an amino group (-NH ₂₎ is substituted, hydrophilicity was expressed. For substitution of this amino group, see AT
As a result of infrared absorption spectrum measurement by R-FTIR,
It was confirmed by the absorption of NH 3500 cm ^-1 .
For defluorination, X-ray photoelectron spectroscopy (XPS)
Confirmed by. At this time, the ArF laser energy density was 20 mJ / cm ² , and the contact angle with water was 5 degrees. When this surface-modified fluororesin sheet sample was adhered to a stainless steel plate via an epoxy resin adhesive and a tensile shear test was performed, an adhesion strength of 140 Kgf / cm ² was confirmed.

(Example 5) A solution prepared by dissolving 2 g of boric acid (H ₃ BO ₃ ) in 50 cc of methyl alcohol was placed in a reaction vessel 6 shown in FIG. 1, and a fluororesin sheet sample was placed therein to prepare a solution and a sample. Irradiation of 15 mJ / cm ² of ArF laser light on the interface with and the contact angle with benzene was 10
The lipophilicity was developed. This surface-modified fluororesin sheet sample was adhered to a stainless steel plate via an epoxy resin adhesive, and a tensile shear test was conducted.
An adhesive strength of 120 Kgf / cm ² was confirmed.

Example 6 A solution prepared by dissolving 2 g of boric acid (H ₃ BO ₃ ) in 50 cc of toluene (C ₆ H ₅ .CH ₃ ) was placed in a reaction vessel 6 shown in FIG. Then, a fluororesin sheet sample was placed therein, and the interface between the solution and the sample was irradiated with ArF laser light. As a result, a lipophilic group similar to that in Example 1 was developed. It was 140 Kgf / c when it was adhered to the board with an epoxy resin adhesive and a tensile shear test was conducted.
An adhesive strength of m ² was confirmed.

(Example 7) 2 g of aluminum hydroxide (Al (OH) ₃ ) was dissolved in a 0.1 N NaOH aqueous solution, and this solution was dipped in a sponge sheet in the same manner as in Example 2 to obtain a solution. A transparent fluororesin (FEP) sheet sample is placed and ArF laser light (10 mJ / cm) is applied from above.
²⁾ it was irradiated with, the expressed similar hydrophilicity Example 2, the surface-modified fluororesin sheet sample was bonded via the Aron Alpha chromatography (TM) stainless steel plate, of 60 kgf / cm ² The adhesive strength was confirmed.

Example 8 Trimethoxyboron (B (O
The CH ₃ ) ₃ ) liquid was placed in the reaction vessel 6 shown in FIG. 1, and a fluororesin sheet sample was placed therein in the same manner as in Example 1, and the interface between the solution and the sample was irradiated with ArF laser light. A contact angle similar to that of Example 1 was obtained, and the treated fluororesin sheet was bonded to a stainless steel plate with an epoxy resin adhesive, and a tensile shear test was conducted.
An adhesive strength of 140 Kgf / cm ² was confirmed.

(Example 9) 2 g of barium hydroxide (Ba)
(OH) ₂ ) is dissolved in 50 cc of water, the solution is dipped in a sponge sheet, and a transparent fluororesin (FEP) is added to the solution.
Place a sheet sample, and from above, ArF laser light (20 m
J / cm ² ), the same hydrophilicity as in Example 2 was developed, and the surface-modified fluororesin sheet sample was adhered to a stainless plate via Aron Alpha (trademark). An adhesive strength of cm ² was confirmed.

Example 10 2 g of gallium acetate (Ga)
(CH ₃ COO) ₃ is dissolved in 50 cc of water, the solution is dipped in a sponge sheet, and the transparent fluororesin (F
(EP) When a sheet sample was placed and irradiated with ArF laser light (20 mJ / cm ² ) from above, the same hydrophilicity as in Example 2 was developed, and this surface-modified fluororesin sheet sample was alon-coated on a stainless steel plate. Alpha (trademark)
When it was adhered via, it was confirmed that the adhesive strength was 25 Kgf / cm ² .

(Example 11) 2 g of lithium acetate (Li
CH ₃ COO) was dissolved in 50 cc of methyl alcohol, this solution was dipped in a sponge sheet, a transparent fluororesin (FEP) sheet sample was placed on the solution, and ArF laser light (20 mJ / cm ² ) was irradiated from above, The same hydrophilicity as in Example 2 was developed, and this surface-modified fluororesin sheet sample was adhered to a stainless steel plate via Aron Alpha (trademark). As a result, 20 Kgf / cm ²
The adhesive strength of was confirmed.

(Example 12) Pure water (H ₂ O) was dipped in a sponge sheet, a transparent fluororesin (FEP) sheet sample was placed on the sponge sheet, and an ArF laser beam (20 mJ / c) was applied from above.
m ² ), the same hydrophilicity as in Example 2 was developed, and this surface-modified fluororesin sheet sample was adhered to a stainless steel plate via Aron Alpha (trademark) to obtain 20 kgf / cm ² The adhesive strength of was confirmed. When the same experiment was repeated using tap water instead of pure water, almost the same results were obtained.

(Example 13) Formic acid (HCOOH) was dipped in a sponge sheet, a transparent fluororesin (FEP) sheet sample was placed thereon, and an ArF laser beam (25 mJ) was applied from above.
/ Cm ² ), the same hydrophilicity as in Example 2 was developed, and this surface-modified fluororesin sheet sample was adhered to a stainless steel plate via Aron Alpha (trademark). An adhesive strength of ² was confirmed.

Example 14 Tetrabenzyl Titanium Ti
₂ g of (CH ₂ C ₆ H ₅ ) _{4 was} added to 50 cc of hexane (C ₆
The solution dissolved in H ₁₄ ) was placed in the reaction vessel 6 shown in FIG.
A fluororesin (FEP) sheet sample was placed in the same manner as in Example 1, and the interface between the solution and the sample was irradiated with ArF laser light. As a result, lipophilicity similar to that in Example 1 was developed, and this surface modification The produced fluororesin sheet sample was adhered to a stainless steel plate with an epoxy resin adhesive and a shear test was conducted. As a result, an adhesion strength of 65 Kgf / cm ² was confirmed.

(Example 15) Formic acid (HCOOH) was dipped in a sponge sheet, a transparent fluororesin (FEP) sheet sample was placed on the sponge sheet, and condensed (diameter about 10 mm) by a reflecting mirror having an upper or toroidal surface and a lens. 100W
When the sample was irradiated with light from a low-pressure mercury lamp for 3 minutes, the same hydrophilicity as in Example 2 was developed. When this surface-modified fluororesin sheet sample was adhered to a stainless plate via Aron Alpha (trademark), 20 Kgf was obtained. An adhesive strength of / cm ² was confirmed.

[0033]

As described in detail above, according to the present invention,
An atom whose binding energy with a fluorine atom is larger than 128 Kcal / mol which is a binding energy between a carbon atom and a fluorine atom, for example, B, Al, Ba, Ga, Li,
A solution having H, Ti and a functional group having an affinity for the adhesive, for example, —OH, —Cl, —NO ₂ is brought into contact with the surface of the fluororesin material, and in that state, the fluororesin material and the solution are separated. The interface is irradiated with ultraviolet rays having a photon energy of 128 Kcal or more, thereby defluorinating the fluororesin material and, at the same time, substituting this functional group for surface modification treatment, and then interposing another material and an adhesive. Since they are bonded together, the fluororesin material can be adhered to the same kind or different kinds of materials with extremely high adhesive strength without damaging the original characteristics of the fluororesin material. As a result, it is possible to provide a fluororesin material composite having excellent chemical resistance by competing the fluororesin sheet on the surface of the structure such as epoxy resin, bakelite, ABS resin, concrete or metal.

As a result, it can be widely used in the chemical plant, the chemical industry, the electrical parts industry, the gas industry, the electric power industry, etc. in the wall surfaces of chemical plants where mechanical strength is required, chemical laser vessels, high voltage equipment, printed circuit boards, etc. It is possible to expand the application of fluororesin for various purposes.

[Brief description of drawings]

FIG. 1 is a schematic diagram of a fluororesin surface treatment apparatus used for carrying out the method of the present invention.

FIG. 2 is a diagram showing the properties of a fluororesin surface treated by the method of the present invention.

FIG. 3 is a perspective view of a fluororesin surface treatment apparatus used for carrying out the method of the present invention.

FIG. 4 is a diagram showing the properties of the fluororesin surface treated by the method of the present invention.

[Explanation of symbols]

 1 ... Excimer laser device 2 ... Mask 3 ... Mirror 4, 5 ... Lens 6 ... Reaction container 7 ... Fluororesin sheet

Claims (14)

[Claims] 1. Prior to bonding a fluororesin material to the same or different materials through an adhesive, an atom having a binding energy with a fluorine atom of 128 Kcal / mol or more, a hydrophilic group, a lipophilic group or the adhesive The fluororesin material is brought into contact with a solution containing a compound having a functional group specific to the agent, and in that state, the interface between the fluororesin material and the solution is irradiated with ultraviolet light having a photon energy of 128 Kcal or more,
Thus, a method for adhering a fluororesin material, characterized in that the fluororesin material is defluorinated, and at the same time, a surface modification treatment is carried out to substitute a functional group having an affinity for the adhesive. 2. The adhesion of the fluororesin material according to claim 1, wherein the compound is selected from a boron compound, an aluminum compound, a barium compound, a gallium compound, a lithium compound, a hydrogen compound and a titanium compound. Method. 3. The compound is (BHNH) ₃ , LiBH
_{4, NaBH 4, KBH 4,} CsBH 4, H 3 BO 3,
_{B (CH 3) 3, B} (C 2 H 5) 3, B (C 3 H 7)
₃ , B (C ₄ H ₉ ) ₃ , B (C ₆ H ₅ ) ₃ , B (OH)
_{2 (C 6 H 5),} NaB (C 6 H 5) 4, B (CH 3
O) ₃ , B (C ₂ H ₅ O) ₃ , B (C ₄ H ₉ O) ₃ ,
(NH ₄ ) ₂ B ₄ O ₇ , Al (OH) ₃ , Al (NO
₃ ) ₃ , AlCl ₃ , AlBr ₃ , AlI ₃ , Al ₂
(SO ₄ ) ₃ , Al (CH ₃ COO) ₂ OH, Al ₂ B
aO ₄ , NH ₄ AlCl ₄ , LiAlH ₄ , AlNa
(SO ₄ ) ₂ , AlK (SO ₄ ) ₂ , Al (NH ₄ ) S
O ₄ , Al (CH ₃ ) ₃ , Al (C ₃ H ₇ ) ₃ , Al
(C ₂ H ₅ ) ₃ , Al (C ₆ H ₅ ) ₃ , Al (C ₂ H ₅
O) ₃ , Al (C ₃ H ₇ O) ₃ , Al (C ₄ H ₉ O)
₃ , Ba (ClO ₄ ) ₂ , BaBr, BaI ₂ , Ba
(OH) ₂ , BaS ₂ O ₃ , Ba (NO ₂ ) ₂ , Ba
(CN) ₂ , GaCl ₃ , GaBr, Ga (OH) ₃ ,
Ga (SO ₄ ) ₃ , Ga (NO ₃ ) ₃ , Ga (CH ₃ C
OO) ₃ , GaK (SO ₄ ) ₂ , Ga (CH ₃ ) ₃ , G
a (C ₂ H ₅ ) ₃ , Ga (C ₃ H ₇ ) ₃ , Ga (C ₄ H
₉ ) ₃ , Ga (C ₆ H ₅ ) ₃ , LiCl, LiBr, L
iI, LiOH, LiSH, LiN, LiNO ₃ , Li
(CH ₃ ), Li (hydrocarbon compound), Li (C ₆ H
_{5), LiCH 3 O, LiAlH} [OC (CH 3) 3]
₃ , LiNH ₂ , H ₂ O, D ₂ O, H ₂ O ₂ , HCOO
H, CH ₃ COOH, HCl, HNO ₃ , H ₂ SO ₄ ,
_{C 6 H 6, C 6 H} 5 CH 3, Ti (CH 2 C 6 H 5)
₄ , [Ti (C ₆ H ₅ ) ₂ ] ₂ , TiCl ₃ , TiBr
_The method for adhering a fluororesin material according to claim 1, which is selected from Ti ₄ and TiI ₄ . 4. As a solvent, water, heavy water, ammonia, sulfuric acid, carbon tetrachloride, hydrogen disulfide, hydrocarbons, halogen compounds, alcohols, phenols, organic acids and their derivatives, nitriles, nitro compounds. The method for adhering a fluororesin material according to claim 1, wherein an amine, an amine and a sulfur compound are used. 5. The method for adhering a fluororesin material according to claim 1, wherein the ultraviolet light having a photon energy of 128 Kcal or more is ArF excimer laser. 6. An ArF excimer laser is transformed into a linear beam by a cylindrical lens, and the linear beam is irradiated along the interface of the fluororesin material continuously pulled up from the solution with the solution. A method for adhering a fluororesin material as described above. 7. The method for adhering a fluororesin material according to claim 5, wherein ArF excimer laser is irradiated through a pattern corresponding to the adhering portion of the fluororesin material. 8. The functional group is --OH, --Cl, --NO.
_{2, -CN, -NH 2, -COOH} , -CO, -OCH 3
_{, -OC 2 H 5, -OC 3} H 7, -OC 4 H 9, -C
_{ONH, -CH 3, -C 2 H} 5, -CH 2, -SO 3
_{H, -C 3 H 7, -C} 4 H 9, a method of bonding fluororesin material according to claim 1, wherein those selected from -C ₆ H _5. 9. Ultraviolet light having a photon energy of 128 Kcal or more from an Hg lamp or Hg-Xe lamp, or an ultraviolet light lamp obtained by arc, corona or silent discharge in air, nitrogen or other gas atmosphere. A method for adhering a fluororesin material according to claim 1. 10. The adhesive has an atom having a binding energy with a fluorine atom of 128 Kcal / mol or more, and the interface between the fluororesin material and the adhesive is irradiated with ultraviolet light having a photon energy of 128 Kcal or more, An adhesive layer is formed on the surface of the fluororesin material.
A method for adhering a fluororesin material as described above. 11. The adhesive is premixed with a solution containing a compound having a binding energy with a fluorine atom of 128 Kcal / mol or more and a hydrophilic group, a lipophilic group or a functional group specific to the adhesive. The adhesive layer is formed on the surface of the fluororesin material by applying this to the surface of the fluororesin material, and then irradiating the interface of the application layer with ultraviolet rays having a photon energy of 128 Kcal or more. A method for adhering a fluororesin material as described above. 12. The method according to claim 1, wherein the porous material is impregnated with the solution, and the interface is irradiated with ultraviolet rays having a photon energy of 128 Kcal or more in a state of being in close contact with the fluororesin material. Adhesion method for fluororesin materials. 13. The surface-modified fluororesin material according to claim 1, or the surface-modified fluororesin material and a heterogeneous resin material are pressure-bonded to each other with an organic solvent in which they are soluble. A method for producing a fluororesin composite material, comprising: 14. The binding energy with a fluorine atom is 12
An ink or paint containing a compound having an atom of 8 Kcal / mol or more and a hydrophilic group, a lipophilic group or a functional group specific to the adhesive is applied to a fluororesin material, and an ultraviolet ray having a photon energy of 128 Kcal or more is applied to the interface. A method for marking a fluororesin material, which is characterized by irradiation.