JP2022121268A - Lighting device and its manufacturing method - Google Patents

Abstract

To provide a lighting device capable of reducing the number of components, and its manufacturing method.SOLUTION: A first resin member (1) is a case, a second resin member (4) is a light-transmissive cover, and the first resin member and the second resin member are welded to each other via a primer layer. At least one layer out of the primer layer is a polymerized substance composition layer which is formed of a predetermined polymerized substance composition.SELECTED DRAWING: Figure 5

Description

TECHNICAL FIELD The present disclosure relates to lighting devices and manufacturing methods thereof.

In general, a lighting device installed in a bathroom or outdoors has a waterproof structure to prevent water from entering. For example, Japanese Patent Laying-Open No. 2017-212202 (Patent Document 1) discloses a lighting device that includes a housing, a sealing member, and a cover. This lighting device includes a light-emitting portion, a storage battery, and a power supply circuit in a housing. The sealing member closes the gap between the housing and the cover by being sandwiched between the housing and the cover.

JP 2017-212202 A

As described above, in the case of Patent Literature 1, a sealing member is required to seal between the housing and the cover, so there is a concern that component management becomes complicated accordingly.

The present disclosure has been made in view of the technical background described above, and an object thereof is to provide a lighting device capable of reducing the number of parts and a manufacturing method thereof.

The present disclosure includes the following aspects.

[1] A first resin member having a thermoplastic resin material;
a second resin member having a thermoplastic resin material;
A lighting device comprising one or more primer layers laminated on at least one of the thermoplastic resin material of the first resin member and the thermoplastic resin material of the second resin member,
The first resin member is a case,
The second resin member is a translucent cover,
The first resin member and the second resin member are welded via the primer layer,
The lighting device, wherein at least one layer of the primer layer is a polymer composition layer formed from the following polymer composition (A) or (B).
(A) A polymer composition containing a polymer of a polymerizable composition containing at least one of the following (1) to (7), and a maleic anhydride-modified polypropylene or a modified polyphenylene ether (B) The following (1) A polymer of a polymerizable composition containing at least one of (7), a maleic anhydride-modified polypropylene or a modified polyphenylene ether, and a thermoplastic resin different from the thermoplastic resin constituting the thermoplastic resin material, (1) Combination of difunctional isocyanate compound and diol (2) Combination of difunctional isocyanate compound and difunctional amino compound (3) Combination of difunctional isocyanate compound and difunctional thiol compound (4) Bifunctional Combination of epoxy compound and diol (5) Combination of bifunctional epoxy compound and bifunctional carboxy compound (6) Combination of bifunctional epoxy compound and bifunctional thiol compound (7) Monofunctional radically polymerizable monomer [2] Polymer composition The lighting device according to [1], wherein the material layer is a layer in direct contact with the thermoplastic resin material.
[3] [1] or [2], wherein the polymer composition contains a polymer of a polymerizable composition containing (4), and the diol of (4) is a bifunctional phenol compound; ].
[4] The primer layer of [1] or [3], wherein the primer layer has a curable resin layer formed from a composition containing a curable resin between the polymer composition layer and the thermoplastic resin material. The lighting device according to any one of the preceding claims.
[5] The lighting device according to [4], wherein the curable resin is at least one selected from the group consisting of urethane resins, epoxy resins, vinyl ester resins, and unsaturated polyester resins.
[6] The thermoplastic resin constituting the thermoplastic resin material is at least one selected from the group consisting of polypropylene, modified polyphenylene ether, and polybutylene terephthalate, according to any one of [1] to [5]. lighting system.
[7] Both the first resin member and the second resin member have the primer layer, and the primer layer of the first resin member and the primer layer of the second resin member are welded together. [1] The lighting device according to any one of [6].
[8] Among the monomers constituting the thermoplastic resin constituting the thermoplastic resin material of the second resin member, a monomer occupying the maximum content and the thermoplastic resin material of the first resin member are In the monomers constituting the thermoplastic resin, the monomers occupying the maximum content are the same, and the content of each of the monomers is 70% by mass or more, [1] to [7 ].
[9] The first resin member has a flange portion, the second resin member has a mounting portion, and the flange portion and the mounting portion are welded via the primer layer, [1] The illumination device according to any one of [8].
[10] The thermoplastic resin material of the first resin member or the second resin member includes polypropylene and at least one reinforcing material selected from the group consisting of talc, glass fiber, and carbon fiber, and The lighting device according to any one of [1] to [9], wherein the first resin member or the second resin member has a tensile strength of 40 MPa or more and a Young's modulus of 3 GPa or more.
[11] The thermoplastic resin material of the first resin member or the second resin member contains polyetherimide and at least one reinforcing material selected from the group consisting of talc, glass fiber, and carbon fiber. , the lighting device according to any one of [1] to [9], wherein the first resin member or the second resin member has a tensile strength of 90 MPa or more and a Young's modulus of 3 GPa or more.
[12] The method for manufacturing a lighting device according to any one of [1] to [11], wherein the primer layer is heated, and the heated primer layer forms the first resin member and the second resin member. A method of manufacturing a lighting device, comprising welding the first resin member and the second resin member by press-fitting the first resin member and the second resin member so as to be interposed therebetween.

According to the present disclosure, it is possible to provide a lighting device capable of reducing the number of parts and a manufacturing method thereof.

1 is a perspective view of a lighting device according to an embodiment of the present disclosure; FIG. It is a schematic sectional drawing which shows the illuminating device of one Embodiment. FIG. 4 is a schematic cross-sectional view showing a state in which one primer layer is laminated on a thermoplastic resin material in the first resin member of one embodiment. FIG. 11 is a schematic cross-sectional view showing a state in which a plurality of primer layers are laminated on a thermoplastic resin material in a first resin member of another embodiment; It is a schematic sectional drawing of the state by which the 1st resin member and the 2nd resin member were welded.

Next, embodiments of the present disclosure will be described below with reference to the drawings.

In the present disclosure, joining means joining things together, and adhesion and welding are subordinate concepts thereof. Adhesion means bonding two adherends (objects to be adhered) via an organic material (hardening resin, thermoplastic resin, etc.) such as tape or adhesive. Welding means melting the surface of an adherend such as a thermoplastic resin by heat, and forming a joined state by entanglement and crystallization due to molecular diffusion by contact pressure and cooling.

In the present disclosure, "(meth)acrylic" means acrylic or methacrylic, and "(meth)acrylate" means acrylate or methacrylate.

[Lighting device]
A lighting device 10 shown in FIG. 1 is attached to, for example, a fixture body 12 fixed to the ceiling of a building. The instrument body 12 is connected to a power source (not shown). The lighting device 10 is fixed to the fixture body 12 with bolts (not shown). Various shapes can be selected for the illumination device 10 according to the application. In the example shown in FIG. 1, the illumination device 10 has a long shape having a longitudinal direction L, a width direction W, and a height direction H, and has a case 14 made of thermoplastic resin and a and a cover 16 . The case 14 has terminals 18 on the outside. The terminals 18 are provided at the ends of the case 14 in the longitudinal direction. Terminals 18 of case 14 are electrically connected to terminals (not shown) of instrument body 12 when attached to instrument body 12 . The illumination device 10 is supplied with AC power from the fixture main body 12 side through the terminal 18 .

The case 14 incorporates a power supply unit 20 as shown in FIG. The power supply unit 20 has a power supply circuit and a light emitting section (not shown). The power supply circuit converts AC power supplied from the fixture main body 12 side into DC power. The power supply circuit specifically includes a rectifier circuit, an inverter circuit, and the like. The light emitting section has a substrate and an LED element provided on the substrate.

The case 14 is a container-like member having a bottom portion 22 , side portions 24 provided integrally with the outer edge of the bottom portion 22 along the longitudinal direction L, and an opening on the side opposite to the bottom portion 22 . A light-emitting portion is provided in the opening of the case 14 . An outer edge along the width direction W of the bottom portion 22 is closed by an end portion (not shown) and provided with the terminal 18 . A side portion 24 is connected to the bottom portion 22 at its proximal end and has a collar portion 26 at its distal end. The flange portion 26 has a shape that protrudes outward in the width direction of the case 14 from the tip of the side portion. The collar portion 26 has a joint surface perpendicular to the height direction H. As shown in FIG.

The cover 16 has translucency and is arranged at a position that closes the opening of the case 14 . The cover 16 has an irradiation section 28 on one side in the height direction H and a mounting section 30 on the other side. The light emitted from the LED elements of the power supply unit 20 passes through the irradiation section 28 and is emitted to the outside. The irradiation unit 28 has a rectangular shape when viewed in the height direction, and a curved shape which is outwardly convex when viewed in the longitudinal direction. The mounting portion 30 has a joint surface facing the case 14 and orthogonal to the height direction H. As shown in FIG. The shape of the irradiation unit 28 is not limited to the shape described above, and can be appropriately selected according to the application. For example, the shape viewed from the height direction may be circular or elliptical.

In the present disclosure, lighting device 10 includes case 14 as a first resin member and cover 16 as a second resin member. The case 14 and the cover 16 are welded together at the joint surface of the collar portion 26 and the joint surface of the mounting portion 30 .

Hereinafter, the case 14 is also referred to as the "first resin member 1", and the cover 16 is also referred to as the "second resin member 4".

[First resin member 1]
As shown in FIG. 3, the first resin member 1 of one embodiment is a laminate having a thermoplastic resin material 2 and one or more primer layers 3 laminated on the thermoplastic resin material. . In FIG. 3, at least one layer of the primer layer 3 is a polymer composition layer 3a formed from a specific polymerizable composition.

In the present disclosure, the polymerizable composition is a combination of specific bifunctional compounds, by polyaddition reaction in the presence of a catalyst, or by radical polymerization reaction of specific monofunctional monomers, a thermoplastic structure, That is, it means a composition that forms a linear polymer structure. Unlike curable resins that form a three-dimensional network with a crosslinked structure when polymerized, the polymerizable composition does not form a three-dimensional network with a crosslinked structure and has thermoplasticity.

In the present disclosure, the polymer composition means a composition containing a polymer (linear polymer) having a thermoplastic structure as a main component (90% by mass or more in total). The polymer includes a polymer obtained from a polymerizable composition containing a combination of the specific bifunctional compounds and/or a specific monofunctional monomer, and a polymer obtained by adding maleic anhydride-modified polypropylene to the polymer. , maleic anhydride-modified polypropylene, modified polyphenylene ether, and the like.

The polymer composition layer 3a is formed from a polymer composition containing a polymer of the polymerizable composition, a polymer obtained by adding maleic anhydride-modified polypropylene to the polymer, a maleic anhydride-modified polypropylene, a modified polyphenylene ether, and the like. It is the layer where The polymerizable composition has a thermoplastic structure, i.e., a combination of the specific bifunctional compounds undergoing a polyaddition reaction in the presence of a catalyst, or a radical polymerization reaction of the specific monofunctional monomers. , forming a linear polymer structure.

In the present disclosure, the primer layer 3 includes the thermoplastic resin material 2 of the first resin member 1 and the second resin material having the thermoplastic resin material, which is the other bonding object, as shown in FIG. 5 to be described later. Interposed between the thermoplastic resin material 2 of the first resin member 1 and the thermoplastic resin material of the second resin member 4 when the lighting device 10 (resin-resin bonded body) is obtained by joining and integrating the member 4 and a layer that improves the bonding strength between the thermoplastic resin material 2 of the first resin member 1 and the thermoplastic resin material of the second resin member 4 .

According to the present disclosure, when the second resin member 4 has a thermoplastic resin material made of the same thermoplastic resin as the thermoplastic resin forming the thermoplastic resin material 2, the first resin member 1 and the second resin The member 4 can be firmly welded. When the second resin member 4 has a thermoplastic resin material made of a thermoplastic resin different from the thermoplastic resin forming the thermoplastic resin material 2, generally, the thermoplastic resin material 2 of the first resin member 1 and the second Although the SP values of the thermoplastic resin materials of the two resin members 4 are often separated, the present disclosure also allows such dissimilar thermoplastic resin materials to be strongly welded together.

In the present disclosure, the “same type of thermoplastic resin” means that the monomers constituting the thermoplastic resin have the same monomer that accounts for the maximum content, and the content of each of the monomers is 70 mass. % or more means a thermoplastic resin. “Different thermoplastic resin” means a thermoplastic resin other than “the same type of thermoplastic resin”. In the monomer, a thermoplastic resin in which the monomers occupying the maximum content are different, or the monomers occupying the maximum content are the same, and the content of at least one of the monomers occupying the maximum content is 70 mass % less than the thermoplastic resin.

<Thermoplastic resin material 2>
The thermoplastic resin forming the thermoplastic resin material 2 is not particularly limited.

Examples of thermoplastic resins include polypropylene (PP, SP value: 8.0 (J/cm ³ ) ^1/2 ), polyamide 6 (PA6, SP value: 12.7 to 13.6 (J/cm ³ ) ^{1 /2} ), polyamide 66 (PA66, SP value: 13.6 (J/cm ³ ) ^1/2 ), polyimide (PI), modified polyphenylene ether (m-PPE), polyphenylene sulfide (PPS, SP value: 19 .8 (J/cm ³ ) ^1/2 ), polyetherimide (PEI), polycarbonate (PC, SP value: 9.7 (J/cm ³ ) ^1/2 ), polybutylene terephthalate (PBT, SP value: 20.5 (J/cm ³ ) ^1/2 ) and the like. From the viewpoint of obtaining the effects of the present invention, the thermoplastic resin is preferably at least one selected from the group consisting of polypropylene, modified polyphenylene ether, and polybutylene terephthalate.

In this disclosure, a solubility parameter (SP value) is a value (δ) that provides a numerical prediction of the degree of interaction between materials, defined by the regular solution theory introduced by Hildebrand.

Various methods for calculating the SP value have been proposed. can be done.
δ=(ΣE _coh /ΣV) ^1/2 (1)
Here, δ is the solubility parameter (J ^0.5 /cm ^1.5 ), E _coh is the cohesive energy density (J/mol), V is the molar molecular volume (cm ³ /mol), and Σ is for each atomic group. is the sum of all the atomic groups constituting the monomer. The values of E _coh and V for each atomic group are listed, for example, in Table 7.3 of "Properties of Polymers, Third completely revised edition".

The thermoplastic resin material 2 may further contain at least one selected from the group consisting of fillers and fibers. For example, the thermoplastic resin material 2 may be of a high-rigidity type containing the above thermoplastic resin and at least one reinforcing material selected from the group consisting of talc, glass fiber, and carbon fiber. In an embodiment in which the thermoplastic resin is polypropylene, examples of talc-containing polypropylene include TRC104N (trade name) manufactured by SunAllomer Co., Ltd. Examples of glass fiber-containing polypropylene include PP-GF40- (trade name) manufactured by Daicel Miraise Co., Ltd. 01 F02, and examples of the carbon fiber-containing polypropylene include PP-CF40-11 F008 (trade name) manufactured by Daicel Miraise Co., Ltd.

The glass fiber-containing thermoplastic resin material is a type of glass fiber reinforced resin (GFRP), and the carbon fiber-containing thermoplastic resin material is a type of carbon fiber reinforced resin (CFRP). The thermoplastic resin material containing reinforcing fibers such as glass fiber and carbon fiber may be in the form of molded articles such as sheet molding compounds (SMC) and bulk molding compounds (BMC). SMC is a sheet-shaped molding obtained by impregnating reinforcing fibers such as glass fibers and carbon fibers with a resin composition containing a thermoplastic resin, a low shrinkage agent, a filler, and the like.

<Primer layer 3>
A primer layer 3 is laminated on the thermoplastic resin material 2 .

[Polymer composition layer 3a]
At least one layer of the primer layer 3 is a polymer composition layer 3a formed from a specific polymer composition.

The polymer composition layer 3a can be obtained by coating the thermoplastic resin material 2 with the specific polymer composition or a solution containing the specific polymer composition. When the solution containing the specific polymer composition is applied onto the thermoplastic resin material 2, the polymerizable composition layer 3a can be formed by volatilizing the solvent after application.

The polymer composition layer 3a preferably contains 90% by mass or more, more preferably 95% by mass or more, of the polymer of the specific polymerizable composition.

The specific polymer composition is the following polymer composition (A) or (B).
(A) A polymer composition containing a polymer of a polymerizable composition containing at least one of the following (1) to (7), and a maleic anhydride-modified polypropylene or a modified polyphenylene ether (B) The following (1) A polymer of a polymerizable composition containing at least one of (7), a maleic anhydride-modified polypropylene or a modified polyphenylene ether, and a thermoplastic resin different from the thermoplastic resin constituting the thermoplastic resin material 2, (1) Combination of difunctional isocyanate compound and diol (2) Combination of difunctional isocyanate compound and difunctional amino compound (3) Combination of difunctional isocyanate compound and difunctional thiol compound (4) Bifunctional Combination of epoxy compound and diol (5) Combination of bifunctional epoxy compound and bifunctional carboxy compound (6) Combination of bifunctional epoxy compound and bifunctional thiol compound (7) Monofunctional radically polymerizable monomer

The polymer composition of (A) and (B) preferably contains a polymer of a polymerizable composition containing the above (4), and the above (4) is a bifunctional epoxy resin and a bifunctional phenol A combination with a compound is more preferred.

The compounding ratio of the bifunctional isocyanate compound and the diol in (1) is preferably set so that the molar equivalent ratio of the isocyanate group to the hydroxyl group is 0.7 to 1.5, more preferably 0.5. 8 to 1.4, more preferably 0.9 to 1.3.

The compounding ratio of the bifunctional isocyanate compound and the bifunctional amino compound in (2) is preferably set so that the molar equivalent ratio of the isocyanate group to the amino group is 0.7 to 1.5, and more It is preferably 0.8 to 1.4, more preferably 0.9 to 1.3.

The compounding ratio of the bifunctional isocyanate compound and the bifunctional thiol compound in (3) is preferably set so that the molar equivalent ratio of the isocyanate group to the thiol group is 0.7 to 1.5, and more It is preferably 0.8 to 1.4, more preferably 0.9 to 1.3.

The compounding ratio of the difunctional epoxy compound and the diol in (4) is preferably set so that the molar equivalent ratio of the epoxy group to the hydroxyl group is 0.7 to 1.5, more preferably 0.5. 8 to 1.4, more preferably 0.9 to 1.3.

The compounding ratio of the bifunctional epoxy compound and the bifunctional carboxy compound in (5) is preferably set so that the molar equivalent ratio of the epoxy group to the carboxy group is 0.7 to 1.5, more preferably It is preferably 0.8 to 1.4, more preferably 0.9 to 1.3.

The compounding ratio of the bifunctional epoxy compound and the bifunctional thiol compound in (6) is preferably set so that the molar equivalent ratio of the epoxy group to the thiol group is 0.7 to 1.5, and more It is preferably 0.8 to 1.4, more preferably 0.9 to 1.3.

(Bifunctional isocyanate compound)
The bifunctional isocyanate compound is a compound having two isocyanato groups, such as hexamethylene diisocyanate, tetramethylene diisocyanate, dimer acid diisocyanate, 2,4- or 2,6-tolylene diisocyanate (TDI) or a mixture thereof, Examples include diisocyanate compounds such as p-phenylene diisocyanate, xylylene diisocyanate, diphenylmethane diisocyanate (MDI). From the viewpoint of primer strength, the bifunctional isocyanate compound is preferably TDI or MDI.

(diol)
The diol is a compound having two hydroxy groups, and examples thereof include aliphatic glycols such as ethylene glycol, propylene glycol, diethylene glycol and 1,6-hexanediol, and bisphenols such as bisphenol A, bisphenol F and bisphenol S. mentioned. The diol is preferably propylene glycol or diethylene glycol from the viewpoint of the toughness of the primer.

(Bifunctional amino compound)
The bifunctional amino compound is a compound having two amino groups, and examples thereof include bifunctional aliphatic diamines and aromatic diamines. Aliphatic diamines include ethylenediamine, 1,2-propanediamine, 1,3-propanediamine, 1,4-diaminobutane, 1,6-hexamethylenediamine, 2,5-dimethyl-2,5-hexanediamine, 2,2,4-trimethylhexamethylenediamine, isophoronediamine, bis(4-amino-3-methylcyclohexyl)methane, 1,3-diaminocyclohexane, N-aminoethylpiperazine and the like. Examples of aromatic diamines include diaminodiphenylmethane, diaminodiphenylpropane, and the like. The bifunctional amino compound is preferably 1,3-propanediamine, 1,4-diaminobutane, and 1,6-hexamethylenediamine from the viewpoint of primer toughness.

(Bifunctional thiol compound)
The bifunctional thiol compound is a compound having two mercapto groups in the molecule. manufactured by Karenz MT (registered trademark) BD1).

(Bifunctional epoxy compound)
The bifunctional epoxy compound is a compound having two epoxy groups in one molecule. For example, aromatic epoxy resins such as bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol S type epoxy resin, biphenol type epoxy resin, naphthalene type bifunctional epoxy resin, and 1,6-hexanediol diglycidyl ether, etc. Aliphatic epoxy compounds may be mentioned.

The bifunctional epoxy compounds may be used alone or in combination of two or more.

Specifically, Mitsubishi Chemical Corporation "jER (registered trademark) 828", "jER (registered trademark) 834", "jER (registered trademark) 1001", "jER (registered trademark) 1004", "jER (registered trademark) YX-4000" and the like. In addition, an epoxy compound having a special structure can also be used as long as it is bifunctional.

(Bifunctional carboxy compound)
The bifunctional carboxy compound is a compound having two carboxy groups, and examples thereof include oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, isophthalic acid, and terephthalic acid. The bifunctional carboxy compound is preferably isophthalic acid, terephthalic acid, and adipic acid from the viewpoint of primer strength or toughness.

(Monofunctional radically polymerizable monomer)
The monofunctional radically polymerizable monomer is a monomer having one ethylenically unsaturated bond. For example, styrene monomers, α-, o-, m- or p-alkyl, nitro, cyano, amide or ester derivatives of styrene, styrenic monomers such as chlorostyrene, vinyltoluene, divinylbenzene; and ethyl (meth)acrylate. , (meth)methyl acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, hexyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, lauryl (meth)acrylate, (meth)acrylate dodecyl acrylate, cyclopentyl (meth)acrylate, cyclohexyl (meth)acrylate, tetrahydrofuryl (meth)acrylate, acetoacetoxyethyl (meth)acrylate, dicyclopentenyloxyethyl (meth)acrylate, phenoxyethyl (meth)acrylate , glycidyl (meth)acrylate and other (meth)acrylic acid esters. The monofunctional radically polymerizable monomers may be used alone or in combination of two or more. From the viewpoint of the strength or toughness of the primer, the monofunctional radically polymerizable monomer is styrene, methyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, or phenoxyethyl (meth)acrylate, and two of these. A combination of the above is preferred.

When obtaining a radically polymerized product of a monofunctional radically polymerizable monomer, a solvent and, if necessary, an additive such as a coloring agent are included in order to allow the radical polymerization reaction to proceed sufficiently to obtain a desired polymerized product. good too. In this case, the monofunctional radically polymerizable monomer is preferably the main component among the components other than the solvent of the radically polymerizable composition. The main component means that the content of the monofunctional radically polymerizable monomer is 50 to 100% by mass. The content is preferably 60% by mass or more, more preferably 80% by mass or more.

As the polymerization initiator for the radical polymerization reaction, for example, known organic peroxides, photoinitiators and the like are preferably used. A room-temperature radical polymerization initiator that combines an organic peroxide with a cobalt metal salt or an amine may also be used. Organic peroxides include those classified as ketone peroxides, peroxyketals, hydroperoxides, diallyl peroxides, diacyl peroxides, peroxyesters, or peroxydicarbonates. As the photoinitiator, it is desirable to use a photoinitiator capable of initiating polymerization within the wavelength range from ultraviolet rays to visible rays.

The radical polymerization reaction is preferably carried out by heating at room temperature to 200° C. for 5 to 90 minutes, depending on the type of reaction compound. In the case of photocuring, a polymerization reaction is carried out by irradiating ultraviolet rays or visible light.

By laminating the polymer composition layer 3a as the primer layer 3 on the thermoplastic resin material 2, the thermoplastic resin material 2 and the same or different thermoplastic resin material are firmly bonded. It can be welded. In particular, the polymer composition layer 3a is preferably a layer in direct contact with the thermoplastic resin material 2. As shown in FIG.

As the polymer composition, it is preferable to select a composition containing a thermoplastic resin that is the same as or similar to the thermoplastic resin that constitutes the thermoplastic resin material 2 . For example, when the thermoplastic resin material 2 is polypropylene, stronger welding can be achieved by using a polymer composition containing maleic anhydride-modified polypropylene. When the thermoplastic resin material 2 is modified polyphenylene ether, stronger welding can be achieved by using a polymer composition containing modified polyphenylene ether.

The primer layer 3 can also be composed of multiple layers including the polymer composition layer 3a. When the primer layer 3 is composed of a plurality of layers, it is preferable to laminate such that the essential polymer composition layer 3a is the outermost surface on the side opposite to the thermoplastic resin material 2 .

(Polymer composition layer A)
The polymer composition layer A, which is one embodiment of the polymer composition layer 3a, is formed from the polymer composition (A).

The polymer constituting the polymer composition layer A is obtained by polyaddition reaction of at least one of the above (1) to (6) in the presence of a catalyst in a solution of maleic anhydride-modified polypropylene or modified polyphenylene ether. can be done. As catalysts for the polyaddition reaction, for example, tertiary amines such as triethylamine and 2,4,6-tris(dimethylaminomethyl)phenol, and phosphorus compounds such as triphenylphosphine are preferably used. The polyaddition reaction is preferably carried out by heating at room temperature to 200° C. for 5 to 120 minutes, depending on the composition of the composition.

Specifically, the polymer composition layer A is a mixture of a polymerizable composition containing at least one of the above (1) to (6) and maleic anhydride-modified polypropylene or modified polyphenylene ether, and a thermoplastic resin. A polyaddition reaction may be preformed prior to application to the material 2 , and a mixture containing the reactants may be applied onto the thermoplastic resin material 2 to form the mixture.

The polymer constituting the polymer composition layer A is obtained by subjecting the composition containing the monofunctional radically polymerizable monomer (7) to a radical polymerization reaction in a solution of maleic anhydride-modified polypropylene or modified polyphenylene ether. can also The radical polymerization reaction is preferably carried out by heating at room temperature to 200° C. for 5 to 90 minutes, depending on the composition of the composition. In the case of photocuring, a polymerization reaction is carried out by irradiating ultraviolet rays or visible light.

Specifically, the polymer composition layer A is formed by mixing the polymerizable composition containing the monofunctional radically polymerizable monomer (7) with maleic anhydride-modified polypropylene or modified polyphenylene ether and heating the mixture. The resulting mixture containing the radically polymerized reaction product can be applied onto the thermoplastic resin material 2 to form a coating.

(maleic anhydride-modified polypropylene)
The maleic anhydride-modified polypropylene is polypropylene graft-modified with maleic anhydride. Examples thereof include Kayabrid 002PP, 002PP-NW, 003PP, 003PP-NW manufactured by Kayaku Akzo Co., Ltd., and Modic series manufactured by Mitsubishi Chemical Corporation. BYK SCONA TPPP2112GA, TPPP8112GA, or TPPP9212GA may also be used as a maleic anhydride functionalized polypropylene additive.

(modified polyphenylene ether)
A known modified polyphenylene ether can be used. Modified polyphenylene ether is a blend of polystyrene, polyamide, polyphenylene sulfide, polypropylene, etc., in polyphenylene ether. Zylon series (PPE/PS, PP/PPE, PA/PPE, PPS/PPE, PPA/PPE), Mitsubishi Engineering-Plastics Epiace series, Lemalloy series (PPE/PS, PPE/PA), etc. be done.

The total amount of (1) to (7) used when obtaining the polymer composition layer A is 5 to 100 parts by mass when maleic anhydride-modified polypropylene or modified polyphenylene ether is 100 parts by mass. is preferred, 10 to 60 parts by weight is more preferred, and 20 to 40 parts by weight is even more preferred.

(Polymer composition layer B)
The polymer composition layer B, which is one embodiment of the polymer composition layer 3a, is formed from the polymer composition (B).

The polymer composition layer B is formed by polyaddition reaction of at least one of the above (1) to (6) in the presence of a catalyst in a solution of maleic anhydride-modified polypropylene or modified polyphenylene ether, and then the thermoplastic resin material 2. It can be obtained by mixing with a thermoplastic resin different from the thermoplastic resin constituting the. In a solution containing a thermoplastic resin different from the thermoplastic resin constituting the thermoplastic resin material 2, at least one of (1) to (6) is subjected to a polyaddition reaction in the presence of a catalyst, and then maleic anhydride is added. It can also be obtained by mixing with modified polypropylene or modified polyphenylene ether. Polyaddition reaction of maleic anhydride-modified polypropylene or modified polyphenylene ether, a thermoplastic resin different from the thermoplastic resin constituting the thermoplastic resin material 2, and at least one of the above (1) to (6) in the presence of a catalyst. You can also get it. As catalysts for the polyaddition reaction, for example, tertiary amines such as triethylamine and 2,4,6-tris(dimethylaminomethyl)phenol, and phosphorus compounds such as triphenylphosphine are preferably used. The polyaddition reaction is preferably carried out by heating at room temperature to 200° C. for 5 to 120 minutes, depending on the composition of the composition.

Specifically, the polymer composition layer B includes maleic anhydride-modified polypropylene or modified polyphenylene ether, a thermoplastic resin different from the thermoplastic resin constituting the thermoplastic resin material 2, and the above (1) to ( A mixture containing a reaction product obtained by heating a mixture with a polymerizable composition containing at least one of 6) can be applied onto the thermoplastic resin material 2 to form the mixture.

The polymer composition layer B comprises a composition containing the monofunctional radically polymerizable monomer (7), maleic anhydride-modified polypropylene or modified polyphenylene ether, and a thermoplastic resin that constitutes the thermoplastic resin material 2. It can also be obtained by a radical polymerization reaction in a solution containing different thermoplastic resins. The radical polymerization reaction is preferably carried out by heating at room temperature to 200° C. for 5 to 90 minutes, depending on the composition of the composition. In the case of photocuring, a polymerization reaction is carried out by irradiating ultraviolet rays or visible light.

Specifically, the polymer composition layer B comprises a polymer of the polymerizable composition containing the monofunctional radically polymerizable monomer (7), maleic anhydride-modified polypropylene or modified polyphenylene ether, and a thermoplastic resin. The thermoplastic resin material 2 can be formed by mixing a thermoplastic resin different from the thermoplastic resin constituting the material 2 and applying a mixture containing a reactant obtained by heating onto the thermoplastic resin material 2 .

The manner of reaction occurring when obtaining the polymer composition forming the polymer composition layer is reaction of maleic anhydride-modified polypropylene or modified polyphenylene ether with bifunctional epoxy resin, maleic anhydride-modified polypropylene or modified polyphenylene. It is also not possible to comprehensively express specific aspects based on a wide variety of combinations, such as reactions between ethers and bifunctional phenol compounds. Therefore, it may be impossible or impractical to directly characterize the polymer composition by structure or properties.

[Curable resin layer 3b]
When the primer layer 3 is composed of a plurality of layers including the polymer composition layer 3a, as shown in FIG. A curable resin layer 3b formed from a composition containing a curable resin may also be included.

The composition containing the curable resin contains a solvent and, if necessary, an additive such as a coloring agent in order to allow the curing reaction of the curable resin to proceed sufficiently to form a desired curable resin layer. You can In this case, the curable resin is preferably the main component among the components other than the solvent of the composition. The main component means that the content of the curable resin is 40 to 100% by mass. The content is preferably 60% by mass or more, more preferably 70% by mass or more, and even more preferably 80% by mass or more.

Examples of the curable resin include urethane resin, epoxy resin, vinyl ester resin, and unsaturated polyester resin.

The curable resin layer 3b may be made of one of these resins, or may be made of a mixture of two or more. The curable resin layer 3b may be composed of a plurality of layers, and each layer may be made of a composition containing different types of curable resins.

Although the coating method for forming the curable resin layer 3b with the composition containing the curable resin monomer is not particularly limited, examples thereof include a spray coating method and an immersion method.

In the present disclosure, the curable resin broadly means a resin that cures by cross-linking, and is not limited to the heat-curing type, and includes room-temperature curing type and photo-curing type. The photo-curing type can also be cured in a short time by irradiation with visible light or ultraviolet rays. The photo-curing type may be used in combination with a heat-curing type and/or a normal temperature-curing type. Examples of the photocurable type include vinyl ester resins such as “Lipoxy (registered trademark) LC-760” and “Lipoxy (registered trademark) LC-720” manufactured by Showa Denko K.K.

(urethane resin)
The urethane resin is usually a resin obtained by reacting an isocyanato group of an isocyanate compound with a hydroxyl group of a polyol compound, and is defined in ASTM D16 as "a coating containing polyisocyanate with a non-volatile content of 10% by weight or more in a vehicle". A urethane resin corresponding to a material is preferable. The urethane resin may be of a one-pack type or a two-pack type.

Examples of one-liquid type urethane resin include oil-modified type (those cured by oxidation polymerization of unsaturated fatty acid groups), moisture-curable type (those cured by reaction between isocyanato groups and water in the air), block type ( isocyanato groups, which are dissociated and regenerated by heating the blocking agent, react with hydroxyl groups to cure), lacquer type (cures by drying after the solvent evaporates), and the like. Among these, moisture-curable one-liquid urethane resins are preferably used from the viewpoint of ease of handling and the like. Specifically, "UM-50P" manufactured by Showa Denko K.K.

Examples of two-component urethane resins include catalyst-curing type (isocyanato groups and water in the air react with each other in the presence of a catalyst to cure), polyol-curing type (reaction of isocyanato groups with hydroxyl groups of polyol compounds, hardened by) and the like.

Examples of the polyol compound in the polyol curing type include polyester polyol, polyether polyol, and phenol resin.

The isocyanate compound having an isocyanato group in the polyol curable type includes, for example, hexamethylene diisocyanate (HDI), tetramethylene diisocyanate, aliphatic isocyanate such as dimer acid diisocyanate; 2,4- or 2,6-tolylene diisocyanate (TDI ) or mixtures thereof, aromatic isocyanates such as p-phenylene diisocyanate, xylylene diisocyanate, diphenylmethane diisocyanate (MDI) or polynuclear mixtures thereof such as polymeric MDI; alicyclic isocyanates such as isophorone diisocyanate (IPDI).

The blending ratio of the polyol compound and the isocyanate compound in the polyol-curing two-component urethane resin is preferably such that the hydroxyl group/isocyanate group molar equivalent ratio is in the range of 0.7 to 1.5.

Examples of the urethanization catalyst used in the two-component urethane resin include triethylenediamine, tetramethylguanidine, N,N,N',N'-tetramethylhexane-1,6-diamine, dimethyl etheramine, N, Amine catalysts such as N,N',N'',N''-pentamethyldipropylene-triamine, N-methylmorpholine, bis(2-dimethylaminoethyl) ether, dimethylaminoethoxyethanol, triethylamine; Organic tin catalysts such as acetate, dibutyltin dilaurate, dibutyltin thiocarboxylate, and dibutyltin dimaleate are included.

In the polyol curing type, it is generally preferable that the urethanization catalyst is blended in an amount of 0.01 to 10 parts by mass with respect to 100 parts by mass of the polyol compound.

(Epoxy resin)
The epoxy resin is a resin having at least two epoxy groups in one molecule. Examples of prepolymers of the epoxy resin before curing include ether-based bisphenol-type epoxy resins, novolac-type epoxy resins, polyphenol-type epoxy resins, aliphatic-type epoxy resins, ester-type aromatic epoxy resins, and cycloaliphatic epoxy resins. , ether-ester type epoxy resins, and the like. Among these, bisphenol A type epoxy resins are preferably used. An epoxy resin may be used independently and may use 2 or more types together.

Specific examples of the bisphenol A epoxy resin include "jER (registered trademark) 828" and "jER (registered trademark) 1001" manufactured by Mitsubishi Chemical Corporation.

Specific examples of the novolak-type epoxy resin include "D.E.N. (registered trademark) 438 (registered trademark)" manufactured by The Dow Chemical Company.

Examples of the curing agent used for the epoxy resin include known curing agents such as aliphatic amines, aromatic amines, acid anhydrides, phenol resins, thiols, imidazoles, and cationic catalysts. By using the curing agent together with a long-chain aliphatic amine and/or thiols, it is possible to form a curable resin layer having a large elongation and excellent impact resistance.

Specific examples of the thiols include the same compounds as exemplified as the thiol compounds for forming the functional group-containing layer described later. Among these, pentaerythritol tetrakis(3-mercaptobutyrate) (for example, "Karenzu MT (registered trademark) PE1" manufactured by Showa Denko KK) is preferable from the viewpoint of elongation and impact resistance of the curable resin layer.

(vinyl ester resin)
The vinyl ester resin is obtained by dissolving a vinyl ester compound in a polymerizable monomer (such as styrene). Also called epoxy (meth)acrylate resins, in the present disclosure, the vinyl ester resins also include urethane (meth)acrylate resins.

As the vinyl ester resin, for example, those described in "Polyester Resin Handbook" (Nikkan Kogyo Shimbun, 1988), "Paint Glossary" (Shikizai Kyokai, 1993), etc. may also be used. can be done. Specific examples include "Lipoxy (registered trademark) R-802", "Lipoxy (registered trademark) R-804" and "Lipoxy (registered trademark) R-806" manufactured by Showa Denko KK.

As the urethane (meth)acrylate resin, for example, after reacting an isocyanate compound and a polyol compound, radicals obtained by reacting a hydroxyl group-containing (meth)acrylic monomer (and optionally a hydroxyl group-containing allyl ether monomer) A polymerizable unsaturated group-containing oligomer is mentioned. Specific examples include "Lipoxy (registered trademark) R-6545" manufactured by Showa Denko K.K.

The vinyl ester resin can be cured by radical polymerization by heating in the presence of a catalyst such as an organic peroxide.

Examples of the organic peroxide include, but are not limited to, ketone peroxides, peroxyketals, hydroperoxides, diallyl peroxides, diacyl peroxides, peroxyesters, peroxy oxydicarbonates and the like. By combining these with a cobalt metal salt or the like, curing at room temperature is also possible.

Examples of the cobalt metal salt include, but are not limited to, cobalt naphthenate, cobalt octylate, and cobalt hydroxide. Among these, cobalt naphthenate and cobalt octylate are preferred.

(unsaturated polyester resin)
The unsaturated polyester resin is a condensation product (unsaturated polyester) obtained by an esterification reaction between a polyol compound and an unsaturated polybasic acid (and saturated polybasic acid if necessary) and a polymerizable monomer (such as styrene). ).

As the unsaturated polyester resin, those described in "Polyester Resin Handbook" (Nikkan Kogyo Shimbun, 1988), "Paint Glossary" (Shikizai Kyokai, 1993), etc. can also be used. can. Specifically, "RIGOLAC (registered trademark)" manufactured by Showa Denko K.K.

The unsaturated polyester resin can be cured by radical polymerization by heating in the presence of the same catalyst as the vinyl ester resin.

[Action of Primer Layer 3]
A primer layer 3 is formed on the surface of the thermoplastic resin material 2 .

Primer layer 3 can provide excellent bondability with second resin member 4 to be bonded. It is also possible to obtain the first resin member 1 capable of maintaining the bondability for a long period of several months. In addition, the surface of the thermoplastic resin material 2 is protected by the primer layer 3, and deterioration such as adhesion of dirt and oxidation can be suppressed.

[Second resin member 4]
The thermoplastic resin forming the thermoplastic resin material of the second resin member 4 may be of the same type as or different from the thermoplastic resin forming the thermoplastic resin material 2 of the first resin member 1 . From the viewpoint of strong welding, these thermoplastic resins are preferably of the same type.

When trying to join two thermoplastic resin materials, even if the thermoplastic resin constituting one thermoplastic resin material and the thermoplastic resin constituting the other thermoplastic resin material are of the same type, one or both If the thermoplastic resin contains fillers or fibers, or if the thermoplastic resin is blended with other thermoplastic resins, according to the prior art, the bond strength between the two thermoplastic resin materials will be inadequate. may be sufficient. According to the present disclosure, even in these cases, the first resin member 1 and the second resin member 4 can be strongly welded via the primer layer 3 (included in the first resin member 1). .

When the thermoplastic resin constituting the thermoplastic resin material 2 of the first resin member 1 and the thermoplastic resin constituting the thermoplastic resin material of the second resin member 4 are of the same kind, a monomer constituting the thermoplastic resin , the ratio of the monomers occupying the maximum content is 70% by mass or more, preferably 70 to 100% by mass, more preferably 80 to 100% by mass, and still more preferably 85 to 100% by mass. .

When the thermoplastic resin material 2 of the first resin member 1 and/or the thermoplastic resin material of the second resin member 4 contains at least one selected from the group consisting of fillers and fibers, the content is preferably 5. to 50% by mass, more preferably 5 to 40% by mass, and even more preferably 5 to 30% by mass. When the content is within the above range, the bonding strength between the first resin member 1 and the second resin member 4 can be increased.

The thermoplastic resin constituting the thermoplastic resin material 2 of the first resin member 1 and/or the thermoplastic resin constituting the thermoplastic resin material of the second resin member 4 is a blend of the main thermoplastic resin and the secondary thermoplastic resin. , the content of the secondary thermoplastic resin is preferably 5 to 40% by mass, more preferably 5 to 30% by mass, and still more preferably 5 to 20% by mass. When the content is within the range, the bonding strength between the first resin member 1 and the second resin member 4 can be increased.

The content rate can be determined by the following formula.
Content rate (mass%) = [B / (A + B)] × 100
(In the formula, A is the mass of the main thermoplastic resin among the thermoplastic resin constituting the thermoplastic resin material 2 of the first resin member 1 and/or the thermoplastic resin constituting the thermoplastic resin material of the second resin member 4 (g), B is the thermoplastic resin constituting the thermoplastic resin material 2 of the first resin member 1 and / or the thermoplastic resin constituting the thermoplastic resin material of the second resin member 4, the secondary thermoplastic It is the mass (g) of the resin.)

According to the present disclosure, even if the thermoplastic resin forming the thermoplastic resin material of the second resin member 4 and the thermoplastic resin forming the thermoplastic resin material 2 of the first resin member 1 are different types, the second The resin member 4 and the first resin member 1 can be strongly welded together. Furthermore, even when the SP value of the thermoplastic resin constituting the thermoplastic resin material of the second resin member 4 and the SP value of the thermoplastic resin constituting the thermoplastic resin material 2 of the first resin member 1 are separated, , the second resin member 4 and the first resin member 1 can be firmly welded.

[Lighting device 10 (resin-resin bonded body)]
FIG. 5 is a schematic cross-sectional view of the state in which the first resin member 1 and the second resin member 4 are welded together. FIG. 4 is a schematic cross-sectional view of a state in which the joint surfaces are welded; The lighting device 10 (resin-resin bonded body) is formed by welding the first resin member 1 and the second resin member 4 via the primer layer 3 (included in the first resin member 1).

As shown in FIG. 5, in the lighting device 10, the primer layer 3 laminated on the thermoplastic resin material of the first resin member 1 (ie case 14) and the second resin member 4 (ie cover 16) are welded together. there is Specifically, the primer layer 3 laminated on the thermoplastic resin material 2 contained in the first resin member 1 and the second resin member 4 are welded so as to be in direct contact with each other. As a result, the space between the first resin member 1 (that is, the case 14) and the second resin member 4 (that is, the cover 16) is sealed.

As described above, the primer layer 3 is formed by the first resin member 1 when the second resin member 4 has a thermoplastic resin material made of the same thermoplastic resin as the thermoplastic resin forming the thermoplastic resin material 2 . and the second resin member 4 are welded together. Therefore, the lighting device 10 of the present disclosure does not require a sealing member for sealing between the case 14 and the cover 16 unlike the conventional lighting device, so that the number of parts can be reduced.

In one embodiment, the first resin member has a collar portion 26 , the second resin member has a mounting portion 30 , and the collar portion 26 and the mounting portion 30 are welded together by the primer layer 3 .

The thermoplastic resin material of the first resin member 1 or the second resin member 4 contains polypropylene and at least one reinforcing material selected from the group consisting of talc, glass fiber, and carbon fiber, and the first resin member 1 Alternatively, it is preferable that the second resin member 4 has properties such as a tensile strength of 40 MPa or more and a Young's modulus of 3 GPa or more.

The thermoplastic resin material of the first resin member 1 or the second resin member 4 contains polyetherimide and at least one reinforcing material selected from the group consisting of talc, glass fiber, and carbon fiber, and the first resin It is preferable that the member 1 or the second resin member 4 have properties such as a tensile strength of 90 MPa or more and a Young's modulus of 3 GPa or more.

The thickness of the primer layer 3 (thickness after drying) depends on the materials of the first resin member 1 and the second resin member 4 and the contact area of the joint portion, but from the viewpoint of obtaining excellent joint strength, it is 1 μm to 1 μm. It is preferably 500 μm, more preferably 3 μm to 100 μm, still more preferably 5 μm to 70 μm. The thickness (thickness after drying) of the polymer composition layer 3a is preferably 1 to 60 μm. When the primer layer 3 has a plurality of layers, the thickness of the primer layer 3 (thickness after drying) is the total thickness of each layer.

As a method for manufacturing the lighting device 10 (resin-resin bonded body), the primer layer 3 of the first resin member 1 is subjected to ultrasonic welding, vibration welding, electromagnetic induction, high frequency, hot plate welding, laser A second resin member 4 is welded by at least one method selected from the group consisting of a method and a hot press method, and a second resin member is formed on the primer layer 3 of the first resin member 1 by injection molding. 4, a method of molding a thermoplastic resin material.

It is advantageous to manufacture the lighting device 10 (resin-resin bonded body) by a heat press method, from the viewpoints of reducing requirements for manufacturing equipment, simplifying the manufacturing process, and increasing the degree of freedom in designing resin members. Specifically, the primer layer 3 is heated, and the first resin member 1 and the second resin member 4 are crimped so that the heated primer layer 3 is interposed between the first resin member 1 and the second resin member 4. Thus, the lighting device 10 (resin-resin bonded body) can be manufactured. The heating temperature of the primer layer depends on the melting point and softening point of the resin to be bonded, and is preferably 100°C to 350°C. For example, when the resin is nylon 6, the heating temperature is preferably 230°C. The primer layer having a melting point is preferably heated at a melting point ±5°C, and the primer layer having a softening point is preferably heated at a softening point ±15°C. The pressure during crimping is preferably 0.01 MPa to 10 MPa.

In another embodiment, the second resin member 4 instead of the first resin member 1 may have one or more primer layers laminated to the thermoplastic resin material. As the primer layer 3 ′ of the second resin member 4 , the same material as the primer layer 3 described above can be used. In this embodiment, the welding of the first resin member 1 and the second resin member 4 is performed by replacing the above-described "first resin member 1" with the "second resin member 4" in this embodiment and the above-described "second resin member 4". 4” can be read as “first resin member 1” in this embodiment.

In yet another embodiment, both the first resin member 1 and the second resin member 4 have the primer layers 3, 3' described above, and the primer layer 3 of the first resin member 1 and the primer layer of the second resin member 4 layer 3' is welded. In this embodiment, the thermoplastic resin forming the thermoplastic resin material 2 of the first resin member 1 and the thermoplastic resin forming the thermoplastic resin material of the second resin member 4 may be of the same type. It may be heterogeneous. In this embodiment, the lighting device 10 (resin-resin joint) is made of at least one selected from the group consisting of ultrasonic welding, vibration welding, electromagnetic induction, high frequency, laser, and heat press. It can be produced by welding the primer layer 3 of the first resin member 1 and the primer layer 3' of the second resin member 4 using a method, preferably a hot press method.

Although several embodiments of the present invention have been described, the present invention is not limited to the above-described embodiments, and various modifications can be made without departing from the gist of the present invention.

Test examples and comparative test examples related to the present invention are shown below, but the present invention is not limited to the following test examples.

<Thermoplastic resin material for test piece>
Under the conditions shown in Table 1 below, using an injection molding machine (SE100V manufactured by Sumitomo Heavy Industries, Ltd.), a thermoplastic resin material for a test piece for a tensile test (width 10 mm, length 45 mm, thickness 3 mm) ): Talc-containing PP resin, m-PPE resin, PC resin, and glass fiber-containing PBT resin were obtained.

<Preparation of test pieces: Examples 1 to 3 and Comparative Examples 1 to 2>
(Preparation of composition-1 for forming primer layer)
A flask was charged with maleic anhydride-modified polypropylene (Modic (registered trademark) ER321P manufactured by Mitsubishi Chemical Corporation): 5 g and xylene: 95 g, and heated to 125° C. with stirring to dissolve. Next, bifunctional epoxy resin (jER (registered trademark) 1001 manufactured by Mitsubishi Chemical Corporation) (bisphenol A type epoxy resin, molecular weight about 900): 1.01 g, bisphenol A: 0.24 g, 2,4,6-tris (Dimethylaminomethyl)phenol: 0.006 g was put into a flask and stirred at 125° C. for 30 minutes to carry out a polyaddition reaction between the bifunctional epoxy resin and bisphenol A. Thus, a composition-1 (hereinafter simply referred to as composition-1) containing maleic anhydride-modified polypropylene and a polymer (thermoplastic epoxy resin) of the bifunctional epoxy resin and bisphenol A was obtained. .

(Preparation of composition-2 for forming primer layer)
A flask was charged with 3.77 g of modified polyphenylene ether (NOLYL731 manufactured by SABIC) and 95 g of xylene, and the temperature was raised to 125° C. with stirring to dissolve. Next, bifunctional epoxy resin (Mitsubishi Chemical Corporation jER (registered trademark) 1001): 1.0 g, bisphenol A: 0.22 g, 2,4,6-tris (dimethylaminomethyl) phenol: 0.005 g The mixture was put into a flask and stirred at 125° C. for 30 minutes to carry out a polyaddition reaction between the bifunctional epoxy resin and bisphenol A. Thus, composition-2 (hereinafter simply referred to as composition- 2) was obtained.

(Formation of primer layer)
Next, composition-1 is applied to the surface of one side of the thermoplastic resin material for the test piece, PP (30% by mass of talc) or PBT (30% by mass of glass fiber), so that the thickness after drying is 80 μm. It was applied by a spray method. After volatilizing the solvent (xylene) by leaving it in the air at room temperature for 30 minutes, heating it in a furnace at 150 ° C. for 30 minutes and allowing it to cool to room temperature. Test piece having composition-1 as a primer layer. PP-1 and PBT-1 were obtained.

Composition-2 was applied to one surface of the m-PPE of the thermoplastic resin material for the test piece by a spray method so that the thickness after drying was 80 μm. After volatilizing the solvent (xylene) by leaving it in the air at room temperature for 30 minutes, heating it in a furnace at 150 ° C. for 30 minutes, allowing it to cool to room temperature, and using Composition-2 as a primer layer. m-PPE-1 was obtained.

Hereinafter, the surface of the test piece on which the primer layer is formed is referred to as the primer surface, and the surface on which the primer layer is not formed is referred to as the non-primer surface. In addition, in Table 2 below, a surface having a primer layer is indicated as (present), and a surface having no primer layer is indicated as (absent).

<Test Example 1>
(welding)
The primer surface of PP-1 and the primer surface of m-PPE-1 are overlapped so that the joint portion overlaps so that the length is 5 mm and the width is 10 mm. - Ultrasonic welding was performed using JII430T-M (28.5 KHz) to obtain a test piece 1 (resin-resin bonded body). Here, the joint portion means a portion where the thermoplastic resin material for the test piece is superimposed.

(Tensile shear strength)
After leaving the test piece 1 at room temperature for 1 day, in accordance with ISO 19095 1-4, a tensile tester (autograph universal testing machine "AG-IS" manufactured by Shimadzu Corporation, load cell 10 kN, tensile speed 10 mm / min, A tensile shear strength test was performed at a temperature of 23° C. and 50% RH to measure the bonding strength. The measurement results are shown in Table 2 below.

<Test Example 2>
(welding)
The primer surface of PP-1 and the primer surface of PBT-1 are overlapped so that the joint overlaps with a length of 5 mm and a width of 10 mm, and an ultrasonic welding machine SONOPET-JII430T manufactured by Seidensha Electronics Industry Co., Ltd. -M (28.5 KHz) was used for ultrasonic welding to obtain a test piece 2 (resin-resin bonded body).

(Tensile shear strength)
The test piece 2 was subjected to a tensile shear strength test in the same manner as in Example 1 of the practical test. The measurement results are shown in Table 2 below.

<Test Example 3>
(welding)
In a state in which the primer surface of m-PPE-1 and one side of the PC of the thermoplastic resin material for the test piece (the surface without primer) are overlapped so that the joint overlaps so that the length is 5 mm and the width is 10 mm, Seiden Ultrasonic welding was performed using an ultrasonic welding machine SONOPET-JII430T-M (28.5 kHz) manufactured by Sha Denshi Kogyo Co., Ltd. to obtain a test piece 3 (resin-resin bonded body).

(Tensile shear strength)
A tensile shear strength test was performed on the test piece 3 in the same manner as in the experimental example 1. The measurement results are shown in Table 2 below.

<Comparative Test Example 1>
The unprimed surface of PP-1 and the unprimed surface of PBT-1 are overlapped so that the joint overlaps with a length of 5 mm and a width of 10 mm. - Ultrasonic welding was attempted using JII430T-M (28.5 KHz), but welding failed.

<Comparative Test Example 2>
The non-primer side of m-PPE-1 and one side (the non-primer side) of the PC of the thermoplastic resin material for the test piece are overlapped so that the joints overlap so that the length is 5 mm and the width is 10 mm. Ultrasonic welding was attempted using an ultrasonic welding machine SONOPET-JII430T-M (28.5 KHz) manufactured by Densha Denshi Kogyo Co., Ltd., but welding was not possible.

<Test Example 4: Test Pieces 4-1 and 4-2>
A thermoplastic resin material m-PPE-1 or PP-1 with a primer is inserted into a mold, PBT is injection molded on the primer surface under the same conditions as in Table 1, and the primer surface and PBT (width 10 mm, length 45 mm thick and 3 mm thick) were obtained.

(Tensile shear strength)
Each test piece was subjected to a tensile shear strength test in the same manner as in Practical Test Example 1. The measurement results are shown in Table 3 below.

INDUSTRIAL APPLICABILITY The present invention can be used for lighting devices and manufacturing methods thereof.

1 first resin member 2 thermoplastic resin material 3 primer layer 3a polymer composition layer 3b curable resin layer 4 second resin member 10 lighting device (resin-resin joint)
12 Apparatus Main Body 14 Case 16 Cover 18 Terminal 20 Power Unit 22 Bottom 24 Side 26 Flange 28 Irradiation Section 30 Mounting Section

Claims (12)

a first resin member having a thermoplastic resin material;
a second resin member having a thermoplastic resin material;
A lighting device comprising one or more primer layers laminated on at least one of the thermoplastic resin material of the first resin member and the thermoplastic resin material of the second resin member,
The first resin member is a case,
The second resin member is a translucent cover,
The first resin member and the second resin member are welded via the primer layer,
The lighting device, wherein at least one layer of the primer layer is a polymer composition layer formed from the following polymer composition (A) or (B).
(A) A polymer composition containing a polymer of a polymerizable composition containing at least one of the following (1) to (7), and a maleic anhydride-modified polypropylene or a modified polyphenylene ether (B) The following (1) A polymer of a polymerizable composition containing at least one of (7), a maleic anhydride-modified polypropylene or a modified polyphenylene ether, and a thermoplastic resin different from the thermoplastic resin constituting the thermoplastic resin material, (1) Combination of difunctional isocyanate compound and diol (2) Combination of difunctional isocyanate compound and difunctional amino compound (3) Combination of difunctional isocyanate compound and difunctional thiol compound (4) Bifunctional Combination of epoxy compound and diol (5) Combination of bifunctional epoxy compound and bifunctional carboxy compound (6) Combination of bifunctional epoxy compound and bifunctional thiol compound (7) Monofunctional radically polymerizable monomer The lighting device according to claim 1, wherein the polymer composition layer is a layer in direct contact with the thermoplastic resin material. 3. Any one of claim 1 or 2, wherein the polymer composition contains a polymer of a polymerizable composition containing (4), and the diol of (4) is a difunctional phenol compound. A lighting device as described. 4. The primer layer according to claim 1, wherein the primer layer has a curable resin layer formed from a composition containing a curable resin between the polymer composition layer and the thermoplastic resin material. lighting device. 5. The lighting device according to claim 4, wherein said curable resin is at least one selected from the group consisting of urethane resin, epoxy resin, vinyl ester resin, and unsaturated polyester resin. The lighting device according to any one of claims 1 to 5, wherein the thermoplastic resin constituting the thermoplastic resin material is at least one selected from the group consisting of polypropylene, modified polyphenylene ether, and polybutylene terephthalate. . 2. Both of said first resin member and said second resin member have said primer layer, and said primer layer of said first resin member and said primer layer of said second resin member are welded together. 7. The lighting device according to any one of 1 to 6. Among the monomers constituting the thermoplastic resin constituting the thermoplastic resin material of the second resin member, a monomer occupying the maximum content and a heat constituting the thermoplastic resin material of the first resin member Any one of claims 1 to 7, wherein the monomers constituting the plastic resin are the same as the monomers occupying the maximum content, and the content of each of the monomers is 70% by mass or more. The lighting device according to the paragraph. The first resin member has a flange portion, the second resin member has a mounting portion, and the flange portion and the mounting portion are welded via the primer layer. A lighting device according to any one of the preceding items. The thermoplastic resin material of the first resin member or the second resin member includes polypropylene and at least one reinforcing material selected from the group consisting of talc, glass fiber, and carbon fiber, and the first resin The lighting device according to any one of claims 1 to 9, wherein the member or the second resin member has a tensile strength of 40 MPa or more and a Young's modulus of 3 GPa or more. The thermoplastic resin material of the first resin member or the second resin member contains polyetherimide and at least one reinforcing material selected from the group consisting of talc, glass fiber, and carbon fiber, and The lighting device according to any one of claims 1 to 9, wherein the first resin member or the second resin member has a tensile strength of 90 MPa or more and a Young's modulus of 3 GPa or more. 12. The method of manufacturing a lighting device according to claim 1, wherein the primer layer is heated, and the heated primer layer is placed between the first resin member and the second resin member. A method of manufacturing a lighting device, comprising: welding the first resin member and the second resin member by pressure bonding the first resin member and the second resin member so as to interpose the first resin member and the second resin member.

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