JPH0318515B2 - - Google Patents
Info
- Publication number
- JPH0318515B2 JPH0318515B2 JP28139685A JP28139685A JPH0318515B2 JP H0318515 B2 JPH0318515 B2 JP H0318515B2 JP 28139685 A JP28139685 A JP 28139685A JP 28139685 A JP28139685 A JP 28139685A JP H0318515 B2 JPH0318515 B2 JP H0318515B2
- Authority
- JP
- Japan
- Prior art keywords
- coating film
- resin molded
- resin
- soft
- coating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000000576 coating method Methods 0.000 claims description 54
- 239000011248 coating agent Substances 0.000 claims description 52
- 229920005989 resin Polymers 0.000 claims description 42
- 239000011347 resin Substances 0.000 claims description 42
- 239000008199 coating composition Substances 0.000 claims description 18
- 239000005056 polyisocyanate Substances 0.000 claims description 15
- 229920001228 polyisocyanate Polymers 0.000 claims description 15
- 239000004088 foaming agent Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 6
- 238000004381 surface treatment Methods 0.000 claims description 6
- 239000004970 Chain extender Substances 0.000 claims description 5
- 239000000945 filler Substances 0.000 claims description 5
- 238000005422 blasting Methods 0.000 claims description 4
- 230000001680 brushing effect Effects 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000002075 main ingredient Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 description 30
- 239000000463 material Substances 0.000 description 15
- -1 polyethylene adipate Polymers 0.000 description 10
- 235000021189 garnishes Nutrition 0.000 description 8
- 239000010410 layer Substances 0.000 description 8
- 239000003973 paint Substances 0.000 description 8
- 238000011282 treatment Methods 0.000 description 6
- 239000003981 vehicle Substances 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 238000005034 decoration Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000004745 nonwoven fabric Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 239000004952 Polyamide Substances 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 239000002981 blocking agent Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- 239000002649 leather substitute Substances 0.000 description 3
- 239000004005 microsphere Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920005990 polystyrene resin Polymers 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000003094 microcapsule Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
- 239000004632 polycaprolactone Substances 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000921 polyethylene adipate Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920002725 thermoplastic elastomer Polymers 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229920001893 acrylonitrile styrene Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 210000000845 cartilage Anatomy 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 239000012508 resin bead Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
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Object of the Invention (Field of Industrial Application) The present invention relates to a method for manufacturing decorative resin molded products used for vehicle interior parts, residential interior decoration parts, and the like. (Prior art) The surfaces of resin molded products such as vehicle interior parts, such as instrument panels, armrests, and pillar garnishes, are treated with flocking using panels and suede-like finishes for the purpose of protecting and decorating the molded base material. Various decorative treatments have been applied, such as fabric-like synthetic leather, and paint containing fillers such as beads. Furthermore, various decorative treatments are applied to the surfaces of various interior decoration products for homes made of resin molded products for the same purpose as described above. (Problems to be Solved by the Invention) However, the above various decoration processes have the following problems. That is, although the flocked hair has a soft feel, it lacks the solid feel of the material, and moreover, it tends to attract dust due to static electricity. In addition, in the case of applying suede-like or fabric-like synthetic leather, these synthetic leathers must be manufactured in a separate process, and since it is necessary to apply it to match the surface shape of the resin molded product, the winding of the terminal part must be The manufacturing process is complicated, and the cost of the product is high, as many other processes are required, such as embedding treatment, and if the surface shape of the resin molded product is complex, a lot of time is required for pasting. Furthermore, in the case of treatments that apply paint containing resin beads to the surface of a resin molded product to give it a visually soft feel (such as ravi painting), since the paint film itself is hard, The drawback is that it is not soft to the touch and does not provide a luxurious feel. In view of the above problems, the present inventors have conducted repeated research on various decorative materials and paints for resin molded products, and have found that:
The present invention was achieved by discovering a method for manufacturing a resin molded product having a soft decorative skin that has a firm and slimy feel. Structure of the Invention (Means for Solving the Problems) That is, the present invention provides (a) a base material consisting of a block type polyisocyanate pyrepolymer, a foaming agent, a chain extender, (b) Preliminarily drying the coating composition applied to the surface of the resin molded article to form a coating film. (c) heating the coating film to form bubbles in the coating film and curing the coating film; (d) brushing the surface of the cured coating film;
The above-mentioned problems have been solved by devising a method for producing a resin molded article, which comprises the steps of surface treatment by means such as blasting and buffing. (Function) By applying the coating composition of the present invention to the surface of a resin molded article or a resin molded article that has been subjected to the above-mentioned known decoration treatment, pre-drying and heat treatment, the block-type polyisocyanate prepolymer is coated. The block comes off and urethane bonding occurs, and
The foaming agent generates fine bubbles, forming a coating film with a soft texture. In addition, the above coating film, in combination with the action of the filler consisting of microspheres in the coating composition, gives a smooth and slimy feel both in appearance and touch. When the above-mentioned coating film is formed on a product, a decorated skin with a suede-like soft and luxurious feel can be obtained. (Example) First, the coating composition used in the method of the present invention will be explained. As mentioned above, the coating composition includes a main ingredient consisting of a block type polyisocyanate prepolymer,
The main ingredients are a blowing agent, a chain extender, and a filler consisting of minute spherical bodies. Here, the block type polyisocyanate prepolymer is a polyisocyanate prepolymer containing a terminal -NCO group containing alcohols, phenols, acetate, etc. It is a polyisocyanate prepolymer that is inactive at room temperature and obtained by blocking with a blocking agent such as ethyl acetate, ε-caprolactam, diethyl malonate, acetylacetone, hydrocyanic acid, or acidic sodium sulfite. Examples of the polyisocyanate prepolymers include isocyanate prepolymers such as hexamethylene diisocyanate (HMDI), tolylene diisocyanate (TDI), 4,4'-diphenylmethane diisocyanate (MDI), and xylylene diisocyanate (XDI). In particular, a non-yellowing HMDI prepolymer with a molecular weight of about 700 to 5000 is the most suitable isocyanate for forming a soft coating film. In addition, it is preferable to use the above block type polyisocyanate prepolymer by dispersing it in water using a nonionic, anionic or cationic surfactant. In this case, the block type polyisocyanate prepolymer and water A weight ratio of about 1:1 is appropriate. Further, polyester polyols such as polyethylene adipate (PEA), polybutylene adipate (PBA), polyhexamethylene adipate (PHA), polycaprolactone (PCL), and polyoxygen Polyether polyols such as propylene diol (PPG), polytetramethylene glycol ether (PTMG), and polyoxyethylene diol (PEC) can be used, but polyester polyols are suitable for forming soft coatings. However, in the case of polyether-based polyols, it is difficult to obtain coating film strength. In addition, the foaming agent is a chemical foaming agent that thermally decomposes rubber or synthetic resin at a predetermined temperature to generate N 2 , CO 2 , etc., and an organic solvent such as a low-molecular-weight alkane encapsulated in a synthetic resin microcapsule. There is a capsule foaming agent, but it is preferable to use a capsule foaming agent whose temperature can be easily controlled, and the amount thereof is 1 to 50 parts by weight per 100 parts by weight of the dispersion of the block type polyisocyanate prepolymer. be. If the amount of the blowing agent is less than 1 part by weight, the soft texture of the coating film will be poor, and if it exceeds 50 parts by weight, the texture of the coating film will become rough and the abrasion resistance will also decrease. Furthermore, as chain extenders, cationic surfactants with a molecular weight of 400 or more are obtained by reacting higher fatty acids such as stearic acid and behenic acid with amino group-containing compounds such as aminoethylethanolamine, diethyltriamine, and polyethylpolyamine. is appropriate. In addition, the blending amount is 5 to 40 parts by weight per 100 parts by weight of the dispersion of the block type polyisocyanate prepolymer,
If it is less than 5 parts by weight, the soft texture of the coating film will be poor, and 40
If the amount exceeds 1 part by weight, the adhesive strength, abrasion resistance, weather resistance, etc. of the coating film will decrease. Next, we reduce the tackiness of the paint film, giving it a firm, soft texture and reducing its internal friction.
In order to improve weather resistance, it is effective to add a lubricant made of microspheres such as polystyrene, crosslinked polystyrene, and acrylic resin. The particle size of the lubricant is preferably several microns to several hundred microns, and the amount added is 5 to 20 parts by weight, and 5 parts by weight, based on 100 parts by weight of the dispersion of the block type polyisocyanate prepolymer. If the amount is less than 20 parts by weight, the above-mentioned effect will not be obtained, and if it exceeds 20 parts by weight, the soft texture of the coating film will be poor and the cost of the coating composition will be high. Furthermore, the above coating composition contains organic or inorganic pigments or dyes. In addition, various additives that are normally added, such as anti-sag agents, anti-settling agents, and leveling agents, may be added. Next, a resin molded article to which the method of the present invention is applied will be explained. In other words, resin molded products are those obtained by injection molding, blow molding, extrusion molding, and other various molding methods, and the resin base materials include ABS resin, polystyrene resin (PS), vinyl chloride resin (PVC),
Acrylonitrile-styrene copolymer resin (AS),
Thermoplastic resins such as ethylene-vinyl acetate copolymer resin (EVA), polyethylene (PE), polypropylene (PP), acrylic resin, reaction-curable resins such as urethane resin, epoxy resin, polyester resin, polyamide resin, or phenolic resin, Examples include various synthetic resins such as thermosetting resins such as melamine resins, urea resins, and formaldehyde resins, and thermoplastic elastomers made of the above-mentioned thermoplastic resins and various rubber components may also be used. Further, the resin molded products used in the method of the present invention include those whose surfaces have been previously subjected to a well-known flocking process or those to which a soft decorative skin has been pasted. Next, to explain the method of the present invention in the order of its steps, first, after degreasing the surface to be painted of the resin molded product,
The coating composition is uniformly spray applied. There are various coating methods such as spray coating, dipping, and brush coating, but since it is necessary to form a coating film with a uniform thickness in the method of the present invention, it is preferable to use spray coating. Although the thickness varies depending on the type of resin molded product, it is usually preferably several tens of microns to several hundred microns. In addition, polyolefin thermoplastic resins such as PP and PE, thermoplastic elastomers containing these resins, reaction-curing resins, thermosetting resins, etc. have poor adhesion to paints, so do not use them before applying primer or plasma treatment. Adhesion to the coating composition can be improved by adding a treatment step. Next, leave the resin molded product at room temperature or
Alternatively, the coating film is pre-dried by drying with warm air. In this pre-drying step, it is necessary to dry the coating surface at least until it is dry to the touch.
Otherwise, when the coating surface is heated in the next process, the gas in the blowing agent will scatter from the coating surface, resulting in countless pores forming on the coating surface and loss of smoothness on the coating surface. Become. After preliminary drying, the surface of the coating film is heated at a predetermined temperature. The temperature at this time is the temperature necessary for the blocking agent of the block type polyisocyanate prepolymer to dissociate, and is usually 100°C or higher. Then, when the blocking agent dissociates, the polyisocyanate prepolymer and chain extender react to form urethane bonds and cure the coating film. Further, at this time, the foaming agent foams to form fine bubbles in the coating film, so it is necessary to select a foaming agent that foams at around the dissociation temperature of the blocking agent. Next, after the coating film is completely cured, its surface is treated by brushing, buffing, shot blasting, or the like. Since the texture of the coating surface changes slightly due to the difference in surface treatment means, a wide variety of decorated molded products can be obtained even when the same coating composition is used. FIRST EMBODIMENT Hereinafter, a first embodiment of a manufacturing method of an instrument panel (hereinafter abbreviated as an instrument panel), which is an interior part for a vehicle, will be explained according to FIGS. 1 to 3.
explain. A coating composition was prepared in advance by blending the raw materials shown in Table 1. On the other hand, a vehicle instrument panel base material was manufactured by injection molding polypropylene resin. Then,
A soft intermediate layer made of vinyl chloride resin is coated on the surface side of the instrument panel base material, and a urethane adhesive is applied to the surface of the soft intermediate layer, followed by coloring made of short polyamide fibers with a length of 0.4 mm and a fineness of 1 denier. An instrument panel was manufactured by flocking the pile.
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ãå¹æãçºæ®ããåªããçºæã§ããã[Table] Next, the surface of the instrument panel that had been subjected to the flocking process was air-blown to remove dust and the like adhering to the pile surface, and then the coating composition was uniformly sprayed onto the surface of the instrument panel. Thereafter, it was pre-dried by blowing warm air at about 50°C for 30 minutes to form a coating film with an average thickness of about 100ÎŒ on the pile. This state is shown in FIG. 1. The upper and outer surfaces of the instrument panel base material 1, which is an injection molded product of polypropylene resin and has a substantially U-shaped cross section, are covered with a cartilage intermediate layer 3a made of vinyl chloride resin. . moreover,
An adhesive layer 4 made of a urethane adhesive is coated on the surface of the soft intermediate layer 3a, and colored piles 5 made of short polyamide fibers having a length of 0.4 mm and a fineness of 1 denier are flocked to the adhesive layer 4. has been done. A coating film 6 made of the coating composition is almost uniformly applied to the surface of the pile 5. Next, only the surface of the coating film 6 was heated for 40 seconds at a temperature of about 120°C to 130°C using a hot air dryer. By this heating, the microcapsules of the foaming agent are ruptured, many fine bubbles are formed inside the coating film 6, and the coating film 6 is cured. After the coating film 6 was completely cured, the surface was brushed using a nylon brush to separate one to several flocked piles 5 at a time. If this state is shown in FIGS. 2 and 3, each or several piles 5 have many fine air bubbles 7 inside.
A coating film 6 having the following properties is formed. The surface of the instrument panel has a suede-like appearance and feel with a firm and slimy feel due to the synergistic effect of the soft feel of the pile 5 itself and the soft coating film 6, giving it an unprecedented sense of luxury. I was able to get a new instrument panel. Furthermore, since the surface of the instrument panel is coated with a coating film 6 of urethane resin, it also has the property of being less likely to generate static electricity. In this example, colored pile 5 made of short polyamide fibers with a length of 0.4 mm and a fineness of 1 denier was used, but in general, piles suitable for the method of the present invention have lengths of 0.4 mm and 1 denier.
A pile having a diameter of 0.1 to 1.2 mm and a fineness of 0.1 to 7 denier may be used in addition to the above-mentioned polyamide fibers. As described above, according to the method of this embodiment, the simple process of applying a coating composition to the surface of a resin molded product that has been subjected to flocking processing, and then subjecting it to surface treatment,
A decorated resin molded product having a soft suede-like appearance and feel can be obtained. What's more, the decorative skin has an unprecedented smooth and slimy feel, creating a unique sense of luxury not found in conventional products such as flocked products or synthetic leather. Second Embodiment Figure 4 shows a second embodiment in which the method of the present invention is applied to a center pillar garnish, which is also an interior part for a vehicle. The center pillar garnish is ABS
A nonwoven fabric is integrally attached as an intermediate layer 3b to the surface of a base material 2 made of resin by an in-mold molding method. A backskin-like soft coating film 6 is formed on the surface of the intermediate layer 3b. The method of this example is similar to the first example, in which a coating composition obtained by blending the raw materials shown in Table 1 is spray-coated onto the surface of the nonwoven fabric, and warm air at about 50°C is blown for 30 minutes to prepare the coating composition. Average film thickness on dry nonwoven fabric: approx.
After forming a soft coating film 6 of 150Ό, the coating film 6 was completely cured, and the surface was further brushed using a nylon brush. Therefore, the center pillar garnish obtained by the method of this example has the soft feel and feel of the nonwoven fabric itself constituting the intermediate layer 3b, as well as the feel of the polished coating film 6. The product not only looks soft to the touch, but also has a unique buckskin-like decorative skin that has a firm and slimy feel that non-woven fabrics do not have. Third Embodiment Figures 5 and 6 show a third embodiment in which the method of the present invention is also embodied in a center pillar garnish. Nishi has a base material 2 made of an injection molded product of ABS resin, and a soft coating film 6 having a large number of fine bubbles 7 inside is coated on the surface of the base material 2. In this example method, a coating composition obtained by blending the raw materials shown in Table 1 is spray-coated onto the surface of the base material 2, and the base material is pre-dried by blowing warm air at about 50°C for 30 minutes. After forming a soft coating film 6 with an average thickness of about 100 Όm on the surface of the coating film 2, the coating film 6 was completely cured, and the surface of the coating film 6 was further brushed using a nylon brush. As described above, a large number of fine bubbles 7 are formed inside the coating film 6 obtained by the method of this example, and this, together with the action of the filler made of microspheres, gives it a soft appearance. Not only does it give a soft feel, but it also has a firm, slimy feel to the touch, creating a calm and luxurious feel that cannot be obtained from conventional soft vinyl chloride resin skin materials. It should be noted that the method of the present invention is not limited to the above-mentioned embodiments, and may be modified by variously changing the blending ratio of each raw material in Table 1, or by performing surface treatment such as buffing or blasting instead of the above-mentioned brushing. By employing this method, it is possible to subtly change the texture of the coating film surface. In addition, the method of the present invention is applicable not only to the above-mentioned instrument panels and pillar garnishes, but also to console box slides,
It can be applied to a wide range of resin molded products, such as vehicle interior parts such as armrests and various residential interior decoration products, and in all cases, it has an unprecedented smooth and slimy feel and is decorated with a luxurious feel. You can get the product. Furthermore, since the method of the present invention forms a decorated skin by spray coating, it is possible to easily obtain a decorated skin with a beautiful multicolored pattern by changing the colors of pigments and dyes in the paint composition. There is also an advantage. Effects of the Invention As detailed above, by applying the above manufacturing method to various resin molded products, it is possible to obtain resin molded products that have a firm, slimy feel and a decorative skin that gives a luxurious feel. Demonstrate the effect of what you can do. In addition, there is no need to attach a decorative skin manufactured in a separate process to match the surface shape of the resin molded product, as in the past, and the simple process of painting and surface treatment creates a soft and luxurious finish. This is an excellent invention that also has the effect of reducing the manufacturing cost of the product because a decorative skin can be obtained.
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å³ã第ïŒå³ã¯ç¬¬äºå®æœäŸã®ã»ã³ã¿ãŒãã©ãŒã¬ãŒã
ãã·ãŠã®æé¢å³ã第ïŒå³ã¯ç¬¬äžå®æœäŸãã»ã³ã¿ãŒ
ãã©ãŒã¬ãŒããã·ãŠã®æé¢å³ããŸã第ïŒå³ã¯ç¬¬ïŒ
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ïŒïŒïŒâŠâŠåºæãïŒâŠâŠäžéå±€ãïŒâŠâŠãã€
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FIG. 1 is a schematic sectional view of the instrument panel of the first embodiment, FIG. 2 is a partially enlarged sectional view of FIG. 1,
Fig. 3 is an enlarged sectional view of the coating film applied to the pile, Fig. 4 is a sectional view of the center pillar garnish of the second embodiment, and Fig. 5 is a sectional view of the center pillar garnish of the third embodiment. Sectional view, and Figure 6 is the 5th
It is a partially enlarged sectional view of the figure. 1, 2... Base material, 3... Intermediate layer, 5... Pile, 6... Paint film, 7... Bubbles.
Claims (1)
ãªã€ãœã·ã¢ããŒããã¬ããªããŒãããªãäž»å€
ãšãçºæ³¡å€ãšãé延é·å€ãšã埮å°ã®çç¶äœãã
ãªãå å¡«å€ãšãäž»æåãšããå¡æçµæç©ãå¡åž
ããå·¥çšã (b) åèšæš¹èæ圢åã®è¢«å¡è£ é¢ã«å¡åžãããå¡æ
çµæç©ãäºå也ç¥ããŠå¡èã圢æããå·¥çšã (c) åèšå¡èãå ç±ããããšã«ããå¡èäžã«æ°æ³¡
ã圢æãããšãšãã«åå¡èã硬åãããå·¥çšã (d) åèšç¡¬åãããå¡èã®è¡šé¢ããã©ãã·ã³ã°ã
ãã©ã¹ãåŠçãããæããªã©ã®æ段ã§è¡šé¢åŠç
ããå·¥çšã ãããªãããšãç¹åŸŽãšããæš¹èæ圢åã®è£œé æ¹
æ³ã[Scope of Claims] 1 (a) A resin molded article containing a main ingredient consisting of a block-type polyisocyanate prepolymer, a foaming agent, a chain extender, and a filler consisting of minute spherical bodies on the surface to be painted of a resin molded product. (b) Pre-drying the coating composition applied to the surface of the resin molded article to form a coating film; (c) Heating the coating film. (d) brushing the surface of the cured coating film;
A method for producing a resin molded product, comprising the steps of surface treatment by means such as blasting and buffing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28139685A JPS62140679A (en) | 1985-12-13 | 1985-12-13 | Production of resin molding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28139685A JPS62140679A (en) | 1985-12-13 | 1985-12-13 | Production of resin molding |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62140679A JPS62140679A (en) | 1987-06-24 |
JPH0318515B2 true JPH0318515B2 (en) | 1991-03-12 |
Family
ID=17638558
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28139685A Granted JPS62140679A (en) | 1985-12-13 | 1985-12-13 | Production of resin molding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62140679A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10494761B2 (en) * | 2016-07-12 | 2019-12-03 | University Of Massachusetts | Fiber surface finish enhanced flocked impact force absorbing structure and manufacturing |
-
1985
- 1985-12-13 JP JP28139685A patent/JPS62140679A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS62140679A (en) | 1987-06-24 |
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