JPH0415681B2 - - Google Patents
Info
- Publication number
- JPH0415681B2 JPH0415681B2 JP12625686A JP12625686A JPH0415681B2 JP H0415681 B2 JPH0415681 B2 JP H0415681B2 JP 12625686 A JP12625686 A JP 12625686A JP 12625686 A JP12625686 A JP 12625686A JP H0415681 B2 JPH0415681 B2 JP H0415681B2
- Authority
- JP
- Japan
- Prior art keywords
- foam
- applicator
- layer
- foaming
- cosmetic
- 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
- 239000006260 foam Substances 0.000 claims description 157
- 239000002537 cosmetic Substances 0.000 claims description 82
- 238000005187 foaming Methods 0.000 claims description 67
- 239000007788 liquid Substances 0.000 claims description 61
- 239000000463 material Substances 0.000 claims description 48
- 239000011324 bead Substances 0.000 claims description 41
- 239000002994 raw material Substances 0.000 claims description 38
- 238000004519 manufacturing process Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 10
- 239000004088 foaming agent Substances 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000010419 fine particle Substances 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 70
- 238000000576 coating method Methods 0.000 description 27
- 239000011248 coating agent Substances 0.000 description 26
- 239000011247 coating layer Substances 0.000 description 19
- 229920002635 polyurethane Polymers 0.000 description 16
- 239000004814 polyurethane Substances 0.000 description 16
- -1 or chemical reaction Substances 0.000 description 14
- 229920003002 synthetic resin Polymers 0.000 description 13
- 239000000057 synthetic resin Substances 0.000 description 13
- 238000005498 polishing Methods 0.000 description 11
- 239000000843 powder Substances 0.000 description 11
- 229920001971 elastomer Polymers 0.000 description 9
- 239000005060 rubber Substances 0.000 description 9
- 239000002245 particle Substances 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 8
- 229920000459 Nitrile rubber Polymers 0.000 description 6
- 239000003431 cross linking reagent Substances 0.000 description 6
- 230000007794 irritation Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 244000043261 Hevea brasiliensis Species 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 229920003052 natural elastomer Polymers 0.000 description 5
- 229920001194 natural rubber Polymers 0.000 description 5
- 239000004745 nonwoven fabric Substances 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920003048 styrene butadiene rubber Polymers 0.000 description 5
- 239000004952 Polyamide Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000002174 Styrene-butadiene Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 229920001821 foam rubber Polymers 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 238000004080 punching Methods 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 102000008186 Collagen Human genes 0.000 description 2
- 108010035532 Collagen Proteins 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- 206010040880 Skin irritation Diseases 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
- 235000021240 caseins Nutrition 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920001436 collagen Polymers 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 210000004209 hair Anatomy 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 231100000344 non-irritating Toxicity 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 108090000623 proteins and genes Chemical class 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 238000007763 reverse roll coating Methods 0.000 description 2
- 230000037307 sensitive skin Effects 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
- 239000004945 silicone rubber Substances 0.000 description 2
- 230000036556 skin irritation Effects 0.000 description 2
- 231100000475 skin irritation Toxicity 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002472 Starch Chemical class 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 229940088990 ammonium stearate Drugs 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229940043430 calcium compound Drugs 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000009685 knife-over-roll coating Methods 0.000 description 1
- 239000008206 lipophilic material Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000037311 normal skin Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 229920001308 poly(aminoacid) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000008107 starch Chemical class 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Description
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ãã®ã§ããã[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a cosmetic applicator suitable for applying makeup cosmetics, such as a puff or a tip with a handle, and the manufacture thereof. It is about the method.
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Conventionally, various foams such as foamed polyurethane and foamed rubber have been frequently used as materials for the application portion of cosmetic applicators.
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äžããŠããã Conventionally, when manufacturing cosmetic applicators from foam, a large foam block or sheet is cut or punched into an appropriate size according to the size of the cosmetic applicator, and then the surface of this smaller foam is It is finished into the desired shape of the cosmetic applicator by cutting and polishing.
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ãªãã In general, when various foams such as foamed polyurethane or foamed rubber are molded into a block or sheet, the part that was in contact with the mold or frame surface is called a face membrane, which is not foamed and has no pores. A hard smooth membrane is formed. On the other hand, a cosmetic applicator is used to apply cosmetics to the skin by applying cosmetics to the skin while lightly pressing the tool. However, since the smooth face film cannot contain cosmetics and is hard, this face film is a nuisance. Therefore, if this surface film is present, it must be removed by cutting or polishing to expose the internal porous layer.
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ã«ãããŠã¯ãäžå¯æ¬ ã§ããã As described above, polishing of the foam surface is essential in foam processing for finishing the shape of the applicator or removing the surface film.
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ãã As described above, during processing from large foam blocks or sheets to finished small cosmetic applicators, the foam skeleton forming the foam is cut and polished. Therefore, the cut end of the foam skeleton on the surface of the applicator (that is, the application part) has a sharp point. The thus formed sharp portions on the surface of the applicator cause skin irritation such as tingling and stiffness when applying cosmetics.
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ãææ¡ããã In order to reduce irritation to the skin surface as mentioned above and obtain a cosmetic applicator with a good feeling of use, the applicant has already made the surface of the skeleton of the foam flexible in Japanese Utility Model Publication No. 57-29687. We proposed coating it with synthetic resin.
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ãå°ãªããªãã As mentioned above, by coating the surface of the skeleton of the foam with a flexible synthetic resin, skin irritation such as tingling and stiffness felt when applying cosmetics can be significantly reduced.
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æ€èšãããŠããã Furthermore, various studies have been made to heat-treat the surface of the foam to round off the cut edges of the skeleton that constitutes the foam.
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However, even if the surface of the foam skeleton is coated with a flexible synthetic resin, people with sensitive skin may still experience irritation, and even people with normal skin may experience sensitive skin areas such as around the eyes. There is a need for cosmetic applicators that are even less irritating and easier to use.
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ã§ããã In addition, when covering the surface of the skeleton of a foam pair with a flexible synthetic resin, in order to round off the sharply pointed parts of the foam skeleton on the surface of the applicator with the coating layer, it is better to have a thicker coating layer. However, if the coating layer is too thick, the pores of the foam may be sealed or the applicator may feel stiff, resulting in a poor usability. Conversely, if the thickness of the coating layer is too thin, sharp points will not be rounded, and therefore irritation of the applicator to the skin will not be reduced. Furthermore, when forming a synthetic resin coating layer on a foam in this way, it is necessary to delicately adjust the viscosity, amount of adhesion, etc. of the synthetic resin.
ãŸããå ç±åŠçã«ãã€ãŠåæç«¯ã«äžžã¿ãä»ãã
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ããããå®çšåãããŠããªãã Furthermore, when attempting to round the cut end by heat treatment, the heat treatment is performed near the melting point of the foamed material, which poses the problem of deterioration of the foamed material, and has not been put to practical use.
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ççã«æ¥µããŠæéãèŠããã Furthermore, polishing the foam is extremely inefficient in production. In other words, small particles of abrasive powder particles that have been polished enter the inside of the foam, and therefore, in the subsequent process, suction processing or cleaning treatment is required to remove the abrasive powder particles. It takes time and effort.
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ããã In addition, in cosmetic applicators, the foaming ratio is 5.
Foams with a magnification of ~70 times are generally used, but the smaller the foam's expansion ratio, the finer the texture of the foam and the better it feels on the skin. However, if the foaming ratio is reduced, there is a problem that the entire applicator becomes too hard and the cost increases.
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ããã€ãã In this way, with conventional foam applicators,
There were various problems with both quality and manufacturing process.
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The present invention has been made in view of these backgrounds, and the purpose of the present invention is to solve the conventional problems as described above, and to make it easy to produce and use the finished product. The purpose of the present invention is to provide a cosmetic applicator that is non-irritating and soft to the touch, has a good feel, and is excellent in quality, and to provide a method for producing the same.
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According to the present invention, the applicator body is made of a foam, and the foam layer is coated on the surface of the body and has a foaming ratio smaller than that of the body, and the foam layer has fine particles formed by tearing on the outer surface of the applicator body. The above-mentioned problems have been solved by a cosmetic applicator characterized in that it has a fluff-like nap, and the outer surface with the fluff-like nap serves as a cosmetic application surface.
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æ³ã«ãããåè¿°ã®åé¡ç¹ã解決ããã Further, in the method for manufacturing the applicator, the foaming raw material liquid is brought into a state where it can be foamed mechanically, by mixing a foaming agent or by chemical reaction, and the foaming raw material liquid has a foaming ratio larger than the foaming ratio of the foaming raw material liquid. A sheet-like foam made of foam and a release sheet are bonded together using the foaming raw material liquid, the foaming raw material liquid is brought into a foamed state and at least substantially solidified to form a foamed layer, and then the foamed layer is torn while the A cosmetic applicator characterized in that the release sheet is peeled off, the sheet-like foam becomes the applicator main body, and the foam layer formed on the surface of the sheet-like foam becomes the cosmetic application surface. The manufacturing method solves the above problems.
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According to the present invention, the outer surface of the foam layer formed on the surface of the applicator main body is the cosmetic application surface, and this outer surface has fine fluff-like naps caused by tearing, so it has an extremely soft touch. This makes it a cosmetic applicator that does not irritate the skin.
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ãåºæ¿ããªãã Furthermore, even if the foam skeleton on the surface of the applicator body has sharp cut edges caused by processing, these cut edges are covered with the foam layer, so they do not irritate the skin during application.
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·ãåŸãããã According to the method of the present invention, a foaming raw material liquid is made into a foamable state by mechanical foaming, mixing of a foaming agent, or chemical reaction, and a foam having a foaming ratio larger than the foaming ratio of the foaming raw material liquid is produced. The sheet-like main body and the release sheet are bonded together using the foaming raw material liquid, and the foaming raw material liquid is foamed and at least substantially solidified to form a foam layer, so that the foam layer is fixed to the sheet-like main body on one side. However, the other side is adhered to the release sheet. Therefore, when the release sheet is subsequently peeled off, the foam layer is pulled in opposite directions from both the sheet-like main body and the release sheet in its thickness direction, and is torn into two. When the foam layer is torn, the foam skeleton of the foam layer is completely stretched, that is, a stretching phenomenon occurs, and the foam layer becomes ultra-fine and fluffy, and is cut in a raised state.
Since this fluff-like raised surface is used as the cosmetic application surface of the cosmetic applicator, the fluff-like raised surface comes into contact with the skin when applying the cosmetic, and a cosmetic applicator with a non-irritating and soft touch quality can be obtained.
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æ§èœã«æ¯éãçããããšã¯ãªãã In addition, since the stretching phenomenon of the foam occurs only in the foam layer on the surface of the cosmetic applicator, it does not affect the strength or stiffness of the foam itself of the applicator itself, and the strength of the applicator itself is reduced. There is no problem with performance such as impact resilience or impact resilience.
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ç£å·¥çšãç°¡åãšãªãã In addition, if a foam with a small expansion ratio is simply applied to completely cover the surface of the applicator body,
A non-foaming surface film is formed on the coated surface. However, according to the present invention, the non-foamed surface film of the foamed layer is peeled off at the same time as the release sheet is peeled off, so there is no need to remove the surface film with a knife or polishing as in the past. , there is no need to process the polishing debris generated when removing the surface film, simplifying the production process.
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The present invention will be explained in detail below based on the illustrated embodiments.
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ãæé¢å³ã§ããã FIG. 1 is a sectional view showing an embodiment of the cosmetic applicator of the present invention.
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ã®ã§ããã The cosmetic applicator of this example is a puff with a canopy, and the applicator material 1 manufactured by the method of the present invention, which will be described later, is placed in a circular drawing machine and drawn with a core 7 inserted therein for application. A canopy 5 is attached thereon with an adhesive 6 to form an applicator.
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ãã The applicator material 1 includes an applicator main body 2 made of foam, and a foam layer 3 that is applied to the surface of the main body 2, has a smaller foaming ratio than the main body 2, and has fine fluff-like naps 31 on the surface. The foamed layer 3 is drawn so that the surface having the fluff-like naps 31 becomes the outer surface of the application area.
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瀺ãæé¢å³ã§ããã FIG. 2 is a sectional view showing another embodiment of the cosmetic applicator of the present invention.
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·ãšãããã®ã§ããã The cosmetic applicator of this embodiment is an applicator with a handle, and the applicator material 1 is coated with the core body 9 in such a way that the foam layer 3 having the fluff-like naps 31 becomes the outer surface of the applicator part.
The base of the core 9 and the hem of the applicator material 1 are fitted into the hole of the handle 8 to form an applicator.
第ïŒå³ããã³ç¬¬ïŒå³ã¯ããããæŽã«å¥ã®å®æœäŸ
ã瀺ãæèŠå³ã§ããã FIGS. 3 and 4 are perspective views showing still further embodiments.
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ãŠãåé¡ã¯çããªãã The puffs of these examples are made by punching out the applicator material 1 and polishing the sides of the punched material. The puff shown in FIG. 3 has a foam layer 3 having fluff-like naps 31 on only one side of the applicator body 2. The puff shown in FIG. 4 has a foamed layer 3 having fluff-like naps 31 on both sides of the applicator body 2. Note that since the outer surface of the foam layer 3 having the fluff-like naps 31 serves as the cosmetic application surface, and the side surfaces of the puff do not serve as the cosmetic application surface, no problem occurs even if the side surfaces of the puff are polished.
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·çŽ æã®æé¢å³ã§ããã 5A to 5E are cross-sectional views of the applicator material at each step for explaining the steps of manufacturing the applicator material 1 used in the cosmetic applicator of the present invention.
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60åçšåºŠã®ãã®ã奜éœåã§ããã First, as shown in FIG. 5A, a sheet-like foam 12 that will become the applicator main body 2 is prepared. This sheet-like foam 12 may be one that has been commonly used as a cosmetic applicator, and has a foaming ratio of 7 to 7.
A value of about 60 times is convenient.
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ãã For example, foams of synthetic resins such as polyvinyl chloride, polyester, polyethylene, polyurethane, and polypropylene, NBR (acrylonitrile butadiene rubber), SBR (styrene butadiene rubber), NR (natural rubber), silicone rubber, fluoro rubber, etc. A sheet-like product of rubber foam can be used, and the foam may be appropriately selected depending on the type of cosmetic to be applied, the purpose of the applicator, the shape, etc.
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ãšãã奜ãŸããã¯ïŒã15åçšåºŠã§ããã Next, the foaming raw material liquid is brought into a state where it can be foamed by mechanical foaming, mixing of a foaming agent, or chemical reaction. In this case, the foaming ratio of the foaming raw material liquid is smaller than the foaming ratio of the sheet-like foam 12, preferably about 3 to 15 times.
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æé©ã§ããã The foaming raw material liquid in the present invention is one that can form a foam and has a viscosity suitable for coating. For example, the viscosity is
The one adjusted to around 1000CPS to 4000CPS is optimal for coating.
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ãŽã ãããçŽ ãŽã çãçšããããšãã§ããã The main raw materials for the foaming raw material liquid include synthetic resins such as polyvinyl chloride, polyester, polyethylene, polyurethane, and polypropylene, NBR (acrylonitrile butadiene rubber), SBR (styrene butadiene rubber), NR (natural rubber), silicone rubber, and rubber. Raw rubber or the like can be used.
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·äœçã«ã¯ããããçºæ³¡åææ¶²ãšããŠäŸã
ã°æ¬¡ã®ãã®ãçšããããšãã§ããã More specifically, the following can be used as these foaming raw material liquids, for example.
ïŒ åææš¹èã®å ŽåïŒ
ã¹ãŒããŒãã¬ãã¯ã¹ïŒããªãŠã¬ã¿ã³ïŒ
第äžå·¥æ¥è£œè¬(æ ª)
ãã³ãã€ãã¯ïŒããªãŠã¬ã¿ã³ïŒ
å€§æ¥æ¬ã€ã³ãååŠå·¥æ¥(æ ª)
ãã€ã¯ãã«ïŒã¢ã¯ãªã«ïŒ
å€§æ¥æ¬ã€ã³ãååŠå·¥æ¥(æ ª)
ãã©ã€ããŒã«ïŒã¢ã¯ãªã«ïŒ
ããŒã ã¢ã³ãããŒã¹(æ ª)
ãããã®ãã®ã¯ä¹³åç¶ã®æ¶²ã§ããããããã®æ¶²
ã«æ¶æ©å€ãäŸãã°ãã¡ã©ãã³ããªã«ããªã³æš¹èã
ããªã¢ããç³»æ¶æ©å€ããšããªãã·ç³»æ¶æ©å€ããã
ãã¯ã€ãœã·ã¢ããŒãç³»æ¶æ©å€çã䜵çšããããšã
ã§ããã*For synthetic resin: Superflex (polyurethane)
Daiichi Kogyo Seiyaku Co., Ltd. Bonteitsuku (Polyurethane)
Dainippon Ink & Chemicals Co., Ltd. Dayknal (acrylic)
Dainippon Ink & Chemicals Co., Ltd. Primal (acrylic)
Rohm and Haas Co., Ltd. These are emulsified liquids, and these liquids contain crosslinking agents such as melamine formalin resin,
A polyamide crosslinking agent, an epoxy crosslinking agent, a blocked isocyanate crosslinking agent, etc. can be used in combination.
ïŒ ãŽã ã®çºæ³¡äœã®å ŽåïŒ
ãããŒã«4850ïŒã¹ãã¬ã³ãŽã ïŒæ¥æ¬ãŒãªã³(æ ª)
ãããŒã«LXâ531ïŒã¢ã¯ãªããããªã«ãŽã ïŒ
æ¥æ¬ãŒãªã³(æ ª)
JSRïŒ0560ïŒïŒã¹ãã¬ã³ãŽã ïŒ æ¥æ¬åæãŽã (æ ª)
ãããã¯ä¹³åç¶æ¶²ã§ããããããã®æ¶²ã«ãåŸæ¥
ããç¥ãããŠããå ç¡«å€ããå ç¡«ä¿é²å€ãæ·»å ã
ãã*For rubber foam: Nipole 4850 (styrene rubber) Nippon Zeon Co., Ltd. Nipole LX-531 (acrylonitrile rubber)
Nippon Zeon Co., Ltd. JSR (0560) (styrene rubber) Japan Synthetic Rubber Co., Ltd. These are emulsified liquids, and conventionally known vulcanizing agents and vulcanization accelerators are added to these liquids. .
ãŸããããªãŠã¬ã¿ã³ã®å Žåã¯ãããªãªãŒã«ãŸã
ã¯ããªãšã¹ãã«ãšã€ãœã·ã¢ããŒãååç©ïŒäŸã
ã°ãããªãžã€ãœã·ã¢ããŒããããã¿ã¬ã³ãžã€ãœã·
ã¢ããŒãçïŒãšãçºæ³¡åææ¶²ãšããŠçšããŠããã
ããååŠåå¿ãããŠçºæ³¡äœãšããŠãããã In the case of polyurethane, polyol or polyester and an isocyanate compound (for example, tridiisocyanate, naphthalene diisocyanate, etc.) may be used as a foaming raw material liquid, and these may be chemically reacted to form a foam.
çºæ³¡åæã«ã€ããŠã¯ãåç²§æã®çš®é¡ããã³ç®ç
ã«ããé©å®éžå®ããã°ããã The foaming raw material may be appropriately selected depending on the type and purpose of the cosmetic.
ãŸããåèšçºæ³¡åææ¶²ã«ã¯ãå¡åžé©æ§ãåäžã
ããããå¢ç²å€ãæ·»å ããŠããããåææš¹èçºæ³¡
äœã®åææ¶²ã«ã¯ãå¢ç²å€ãšããŠãã¡ãã«ã»ã«ããŒ
ã¹ãããªã¢ã¯ãªã«é
žãœãŒããã¢ã«ã®ã³é
žãœãŒãã
çšããããŽã çºæ³¡äœã®å Žåã«ã¯ãã«ãŒã€ã³ã¢ã³ã¢
ãã¢æº¶æ¶²çãçšããã Further, a thickener may be added to the foaming raw material liquid in order to improve coating suitability. Methyl cellulose, sodium polyacrylate, and sodium alginate are used as thickeners in the raw material liquid for synthetic resin foam. In the case of rubber foam, a casein ammonia solution or the like is used.
ãã®ããã«ããŠçºæ³¡åææ¶²ã®ç²åºŠã1000CPSã
4000CPSäœã«èª¿æŽãããšãå¡å·¥ã«æé©ã§ããã In this way, the viscosity of the foaming raw material liquid can be adjusted to 1000CPS~
Adjusting to around 4000CPS is optimal for coating.
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ææ¶²ãããªãŒã¯ã¹åãããµãŒã泡ç«ãŠæ©çã§ïŒã
10åã奜ãŸããã¯ïŒãïŒåçšåºŠã«æ©æ¢°çã«çºæ³¡ã
ããŠæçµçãªå¡åžæ¶²ãšããã After blending various additives as necessary, the foaming raw material liquid is mixed with an oak mixer, whisking machine, etc.
The final coating solution is prepared by mechanically foaming the solution to a size of 10 times, preferably 3 to 7 times.
çºæ³¡åææ¶²ãæ©æ¢°çã«çºæ³¡ããã代ãã«ãçºæ³¡
å€ãåææ¶²ã«æ··å
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ãŠå ç±ããããšã«ããçºæ³¡ãããŠãããã Instead of mechanically foaming the foaming raw material liquid, a foaming agent may be mixed into the raw material liquid to form a coating liquid, and foaming may be performed by heating in a subsequent step.
ãŸããããªãŠã¬ã¿ã³ã®ããã«ãããªãªãŒã«ãŸã
ã¯ããªãšã¹ãã«ãšã€ãœã·ã¢ããŒãååç©ãšãæ··å
ããŠå¡åžæ¶²ãšããããããååŠåå¿ãããŠçºæ³¡äœ
ãšããŠãããã Alternatively, like polyurethane, a polyol or polyester and an isocyanate compound may be mixed to form a coating liquid, and the mixture may be chemically reacted to form a foam.
åè¿°ã®ããã«ãçºæ³¡åææ¶²ãæ©æ¢°çã«çºæ³¡ãã
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ã¿ã®å¡åžå±€ïŒïŒã圢æããïŒç¬¬ïŒå³ïŒ¢åç
§ïŒã As described above, the foaming material liquid is mechanically foamed, or a coating liquid made into a foamable state by mixing a foaming agent or a chemical reaction is applied to the sheet-like foam 12 to form the sheet-like foam 12. A coating layer 13 of a constant thickness is formed on the surface (see FIG. 5B).
å¡åžæ¶²ãå¡åžããå Žåããã€ããªãŒããŒããŒã«
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ãŒãç¶çºæ³¡äœïŒïŒã®è¡šé¢ã«å¡åžããããšã奜ãŸã
ãããŸããå¡åžå±€ïŒïŒã®åã¿ã¯0.2mmãïŒmmçšåºŠ
ãšããããã·ãŒãç¶çºæ³¡äœïŒïŒã®çš®é¡ãçºæ³¡å
çã衚é¢ç¶æ
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ããäžè¬ã«0.3mmã1.5mmçšåºŠã奜ãŸããã When applying the coating liquid, an appropriate method such as a roll coating method such as a knife over roll coating method or a reverse roll coating method, a spray coating method, or a dipping method may be used. In either method, in order to obtain a homogeneous foam layer, it is preferable to apply the coating liquid to the surface of the sheet-like foam 12 with a uniform thickness. The thickness of the coating layer 13 is approximately 0.2 mm to 3 mm, but the type of sheet-like foam 12, foaming ratio, surface condition, etc., the type of coating layer 13, viscosity, foaming ratio, etc., and the cosmetic applicator. The appropriate thickness is determined by taking into consideration the type and type of cosmetic to be applied. Generally, about 0.3 mm to 1.5 mm is preferable.
å¡åžå±€ïŒïŒã®åã¿ã®ã³ã³ãããŒã«ã¯åŸæ¥è¡ãªã
ããŠããããã«ããã°ãããäŸãã°ããªããŒã¹ã
ãŒã«ã³ãŒãæ³ã§ã¯ãèšéããŒã«ãšå¡åžããŒã«ã®é
éããå¡åžããŒã«ãšãããã³ã°ããŒã«ã®é床æ¯ç
ã調ç¯ããããŸãããã€ãããŒã«æ³ã§ã¯ããã€ã
ãšã·ãŒãç¶çºæ³¡äœïŒïŒã®ééãã·ãŒãç¶çºæ³¡äœïŒ
ïŒã®èµ°è¡é床ãå¡åžæ¶²ã®ç²åºŠçã調ç¯ããã The thickness of the coating layer 13 may be controlled in a conventional manner. For example, in the reverse roll coating method, the gap between the metering roll and the application roll, the speed ratio between the application roll and the bucking roll, etc. are adjusted. In addition, in the knife roll method, the gap between the knife and the sheet-like foam 12, the sheet-like foam 1
Adjust the running speed, viscosity of the coating liquid, etc. in step 2.
次ãã§ã第ïŒå³ïŒ£ã«ç€ºãããã«ãå¡åžå±€ïŒïŒã®
衚é¢ã«å¥é¢çšã·ãŒãïŒã貌ãåããã Next, as shown in FIG. 5C, a release sheet 4 is attached to the surface of the coating layer 13.
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ç©ãçŽããã€ã«ã 衚é¢ã«æ€æ¯å å·¥ãæœããã·ãŒ
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ããç¹ã«ãå¥é¢çšã·ãŒãïŒã¯ãã®è¡šé¢ãèµ·æ¯ç¶æ
ã®ãã®ãå¹åžãæãããã®ãæãŸããã As the release sheet 4, a woven fabric, a non-woven fabric, a knitted fabric, paper, a sheet whose surface is treated with flocking, a sheet made of a foam, etc. can be used. In particular, it is desirable that the release sheet 4 has a raised surface or an uneven surface.
ãã®ããã«ãå¥é¢çšã·ãŒãïŒã®è¡šé¢ã«èµ·æ¯ãå¹
åžãååšãããšããã®èµ·æ¯éšãå¹åžéšãå¡åžå±€ïŒ
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ïŒâ²ã«å¯Ÿããæéšæ©èœãæããã In this way, if there are raised or uneven surfaces on the surface of the release sheet 4, the raised or uneven parts will cause the coating layer 1 to
Then, when the coating layer 13 is solidified in a foamed state to form the coating layer 13', the raised portions and uneven portions firmly bite into the coating layer 13' and become fixed. In other words, the raised parts and uneven parts are foamed layer 1.
It has an anchoring function for 3'.
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ïŒã«å没ããçšåºŠã«å å§åŠçããããšã奜ãŸã
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質ãäœäžããã In order to bring the release sheet 4 into close contact with the coating layer 13, the raised portions or convex portions of the release sheet 4 are attached to the coating layer 1.
It is preferable to apply pressure treatment to such an extent that it is buried in the 3. Note that the portion of the coating layer 13 to which the release sheet 4 is not completely adhered will be easily peeled off from the release sheet 4 when the release sheet 4 is removed in a later step, and will not be torn when forming a sheet-like foam. body 12
Therefore, the foamed surface film in that area remains on the surface of the sheet-like foam 12, degrading the quality of the finished product.
ãªããåè¿°ãã第ïŒå³ïŒ¢ããã³ïŒ£ã«ãããŠã¯ã
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ãŒãïŒã«çºæ³¡åææ¶²ãå¡åžããŠãããããã«ã·ãŒ
ãç¶çºæ³¡äœïŒïŒã貌ãåããŠãããã In addition, in FIG. 5 B and C mentioned above,
The coating liquid is applied to the sheet-like foam 12 and then the release sheet 4 is attached.However, conversely, the foaming raw material solution is applied to the release sheet 4 and then the sheet-like foam 12 is attached thereto. May be combined.
次ãã§ã第ïŒå³ïŒ€ã«ç€ºãããã«ããã®ç¶æ
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ãŸã§å¡åžå±€ïŒïŒãåºåããã Next, as shown in FIG. 5D, the coating layer 13 is solidified in this state.
ä¹³åç¶ã®åææš¹èæ¶²ãæ©æ¢°çã«çºæ³¡ãããå Ž
åã120âã150âã§10åéã20åéçšåºŠã§åå¿åº
åããã When an emulsified synthetic resin liquid is mechanically foamed, it reacts and solidifies at 120°C to 150°C for about 10 to 20 minutes.
ãŸããä¹³åç¶ã®ãŽã æ¶²ãæ©æ¢°çã«çºæ³¡ãããå Ž
åããéåžžã110âã15åéçšåºŠã®å ç¡«åŠçã«ã
ããçºæ³¡åºåãããããšãã§ããã Furthermore, even when an emulsified rubber liquid is mechanically foamed, it can be foamed and solidified by vulcanization treatment at 110° C. for about 15 minutes.
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ãšãªã€ãŠããã In this way, the sheet-like foam 12 and the release sheet 4 are bonded together with the foam layer 13' present in between, and the raised portions and uneven portions on the surface of the release sheet 4 are formed into the foam layer 13'. It's in a state where it's stuck.
次ã«ã第ïŒå³ïŒ¥ã«ç€ºãããã«ãå¥é¢çšã·ãŒãïŒ
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ã§åããã Next, as shown in FIG. 5E, the release sheet 4
is peeled off from the sheet-like foam 12. The intermediate foam layer 13' adheres to the sheet-like foam 12 on one side,
Since the other side is adhered to the release sheet 4, when the release sheet 4 is peeled off, the foam layer 13' is pulled in the opposite direction from both the sheet-like foam 12 and the release sheet 4 in its thickness direction. As a result, it is torn in two. When the foamed layer 13' is torn, the foamed skeleton of the foamed layer 13' is completely stretched, that is, a stretching phenomenon occurs, and the foamed layer becomes extremely fine and fluffy, and is broken in a raised state.
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ããã«ããã When peeling off the release sheet 4, the foam layer 13'
This is done so that the surface film of the foamed layer 13' is completely stuck to the release sheet 4, that is, the surface film of the foam layer 13' is completely left on the release sheet 4.
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é¢ã«ã¯åŸ®çŽ°ãªæ¯çŸœç¶èµ·æ¯ïŒïŒã圢æãããŠããã FIG. 6 is an enlarged sectional view schematically showing the surface of the foam layer 3 (see FIG. 5F) on the sheet-like foam 12 after the release sheet 4 has been peeled off. In this way, fine fluff-like naps 31 are formed on the surface of the foam layer 3 on the sheet-like foam 12.
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ããã Next, the applicator material 1 manufactured in this way is cut or punched into an appropriate size according to the size of the desired cosmetic applicator, and the fluff-like nap 31
so that the surface having the surface becomes the cosmetic application surface,
Finish into the desired shape of the cosmetic applicator. for example,
It is passed through a circular wringer to form a cosmetic applicator as shown in FIG. 1, a handled applicator as shown in FIG. 2, or a puff as shown in FIG. 3.
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ãå¡åžé¢ãšããŠäœ¿çšã§ããã®ã§äŸ¿å©ã§ããã In the above-mentioned embodiment, the foam layer 13' having the fluffy nap 31 is provided only on one side of the sheet-like foam 12, but the foam layer 13 and the release sheet 4 are provided on both sides of the sheet-like foam 12. Then, when the release sheet 4 is peeled off, a foam layer 13' having fluff-like naps 31 can be formed on both sides of the sheet-like foam 12. In this way, the seventh
An applicator material 1 as shown in the figure can be obtained. This applicator material 1 can be punched out to form a puff as shown in FIG. 4, which is convenient because both sides of the puff can be used as application surfaces.
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ãŠåœ¢æããã FIG. 8 is a sectional view showing another embodiment of the applicator material 1 of the present invention. In this embodiment, an anchor coat layer 10 is provided between the applicator body 2 and the foam layer 3. This anchor coat layer 10 is intended to increase the adhesion strength between the applicator body 2 and the foam layer 3, and is made of synthetic resin such as acrylic, urethane, polyester, polyamide, vinyl, polyolefin, etc. liquid or
It is formed by applying a synthetic rubber liquid such as NBR or SBR or a natural rubber liquid to the surface of the applicator main body 2 by an appropriate method such as spray coating, roll coating, or knife coating.
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ãã€ã«ã ç¶ã«åœ¢æããã The anchor coat layer 10 may be in the form of a film. For example, the anchor coating liquid is applied onto release paper and dried to form a film, which is then adhered to the surface of the applicator main body 2 with an adhesive. or,
When the anchor coat liquid applied on the release paper is semi-dry, it is directly attached to the surface of the applicator main body 2 without adhesive, and when it is completely dry, the release paper is peeled off.
Form into a film.
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·ã§ããã In this case, if you use a liquid-impermeable film,
Even low-viscosity cosmetics such as liquid cosmetics can be prevented from penetrating into the applicator. Therefore, it is an economical cosmetic applicator because it can prevent wasteful consumption of cosmetics.
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æ®µã«æåœ¢ããããã«ããŠãããã Furthermore, as another example, a sheet-like foam 12 is used to adjust the flexibility (waist) etc. during use.
Foamed layer 1 having fluff-like naps 31 once on the surface of
After forming the foam layer 13', a coating liquid is further applied to the surface of the foam layer 13', a release sheet 4 is attached, and the release sheet 4 is peeled off, thereby forming the foam layer 13 having the fluff-like naps 31. ' may be formed in two stages or in multiple stages.
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·ãåŸãããšãã§ããã In this way, a desired cosmetic applicator can be obtained by making various modifications based on the embodiment described in FIGS. 5A to 5F so as to adjust the flexibility, texture, etc. during use. be able to.
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ããªãŒã ã·ãŒãïŒçºæ³¡åçïŒ40åïŒãçšãããExample 1 As the sheet-like foam 12, polyurethane SD
A 7 mm thick foam sheet (expansion ratio: 40 times) from Bridgestone Tire Co., Ltd. was used.
çºæ³¡åææ¶²ãšããŠäžèšæåã䜿çšããã The following components were used as the foaming raw material liquid.
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ããå¡åžæ¶²ãšããã*Main ingredient: Polyurethane emulsion [Superflex 200: Daiichi Kogyo Seiyaku Co., Ltd.] 100 parts: *Foam stabilizer: 30% aqueous solution of ammonium stearate 12 parts *Crosslinking agent: Sumitex-M3 [Sumitomo Chemical Co., Ltd.] 2 parts Sumitex Accelerator ACX [Sumitomo Chemical Co., Ltd.] 0.2 parts After mixing the foaming raw material liquid consisting of the above components, foaming was performed using a foaming machine to a ratio of 2.5 times, and this was used as a coating liquid.
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ã§åºåãããã Apply this coating liquid to the surface of the sheet-like foam 12.
After coating 150g/ m2 with a knife over roll coater, immediately adhere to a polyester nonwoven fabric: Acstar B-504-10P (Toray Industries, Inc.) and heat at 80°C.
After drying for 20 minutes, heat treatment was performed at 140°C for 10 minutes to crosslink the components of the coating solution and solidify them in a foamed state.
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ãªãŒãã¢ã³ããŒã·ãšã³çšããã補é ããã Next, after the sheet obtained in this manner has cooled, the adhered nonwoven fabric is peeled off to obtain an applicator material 1 in which a foam layer 13' having fine fluff-like naps 31 is provided on the surface of the polyurethane sheet 12. Ta.
This applicator material 1 was finished by punching or the like to produce a puff for powder leaf foundation.
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ã確èªã§ããã The puff of this example has a fluffy nap 31 on the application surface, so it has an extremely good feel, and when applying powdered cosmetics, etc., the puff contains much less powder than conventional products of this type. It was also confirmed that the condition was good.
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ããŠè¡šããŠããã FIG. 9 is a sectional view showing still another embodiment of the applicator material 1 according to the present invention, and in this embodiment, spherical beads 32 are mixed in the foam layer 13'. Unlike the example, the spherical beads 32 are inside the skeleton of the foam layer 13' and are also deposited on the surface of the skeleton of the foam layer 13'. In addition, in FIG. 9, the spherical beads 32 are shown enlarged in comparison with the dimensions of the foam skeleton of the foam layer 13'.
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·çŽ æïŒãåŸãããã In order to manufacture the applicator material 1 of this embodiment, the spherical beads 32 may be mixed into the foaming raw material liquid explained with reference to FIG. 5, and the subsequent processing may be carried out in the same manner. That is, the foaming raw material liquid containing the spherical beads 32 is mechanically foamed, or a coating liquid is made into a foamable state by mixing a foaming agent or by chemical reaction. This coating solution containing spherical beads 32 is applied to the sheet-like foam 12, and a foam layer 13 containing spherical beads 32 is applied to the surface of the sheet-like foam 12 to a constant thickness.
A release sheet is attached to this surface,
In this state, the foam layer 13 containing spherical beads 32
is solidified, and then the release sheet is peeled off from the sheet-like foam 12. In this way, the ninth
The applicator material 1 shown in the figure is obtained.
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ãŠèª¬æããã The spherical beads 32 to be mixed into the foaming raw material liquid will be explained.
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å€ãç²Ÿå¯æ¿Ÿéæãªã©ãææ¡ãããŠããã Spherical beads themselves have recently been developed and commercialized, and are almost completely spherical microscopic powder particles.Currently, their uses include fillers, powder lubricants, adsorbents, and precision filtration materials. has been done.
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äžç©ºã®ãã®ãããã Moreover, the spherical beads 32 are not only solid ones, but also porous ones and hollow ones such as microcapsules.
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åç©ïŒéå±ïŒãŽã çã䜿çšããããšãã§ããã The material of the spherical beads 32 used in the present invention is not particularly limited, and examples thereof include polyethylene, polypropylene, polyurethane, polyester, polyamide, polycarbonate, silicone resin, fluororesin, phenolic resin, acrylic resin, polystyrene epoxy resin, vinyl resin, Synthetic resins such as benzoguanamine resin; cellulose compounds; starch compounds; protein compounds such as collagen; calcium compounds; inorganic compounds such as ceramics and glass; metals; rubber, etc. can be used.
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ããã The material of the spherical beads 32 may be appropriately selected depending on the cosmetic to be applied. For example, water-repellent paraffin, polyethylene, silicone resin, fluororesin, etc. are suitable for cream foundations and the like. When a fluororesin having oil repellency is used, cosmetics adhering to the applicator can be easily washed off.
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ã«ãé©ããŠããã Water-absorbing proteins such as cellulose, collagen, and casein are suitable for summer foundations that use water. In addition, using ceramic, glass, phenolic resin, polycarbonate, polystyrene, polypropylene, polyamide, etc., reduces the frictional resistance of the applicator, making it easier to apply and spread cosmetics on the skin, and is also suitable for pine surgery. .
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ããªãã®ãããã Examples of commercially available spherical beads include the following.
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ã20ãã¯ãã³çšåºŠã®ãã®ãé©ããŠããã*Product Name: Fine Pearl, Material: Polystyrene, Manufacturer: Sumitomo Chemical Co., Ltd. *Product Name: Fine Pearl, Material: Acrylic Resin, Manufacturer: Sumitomo Chemical Co., Ltd. *Product Name: Tekuma-MB-2, Material : Polymethyl methacrylate, Manufacturer: Sekisui Plastics Co., Ltd. *Product name: Toray Nylon SP-500, Material: Nylon, Manufacturer: Toray Co., Ltd. *Product name: Flow Beads LE-1080, Material: Polyethylene, Manufacturer: Steel Chemical Industry Co., Ltd. *Product name: Spherical porous silica, Material: Silicic anhydride,
Manufacturer: Suzuki Yushi Kogyo Co., Ltd. *Product name: Glass beads, Material: Glass, Manufacturer: Nippon Electric Glass Co., Ltd. (Shiga Prefecture) The spherical beads 32 used in the present invention are almost completely spherical. Particle sizes of about 0.1 to 1000 microns can be used, preferably an average particle size of 5.
~20 microns is suitable.
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ã«æ±ºå®ããã Furthermore, when porous spherical beads are used, since they have pores, they have excellent water absorption and water retention properties. The amount of spherical beads to be mixed into the foaming raw material depends on the size of the spherical beads, the material of the spherical beads, the type of cosmetics (viscosity, properties, etc.), and the intended use of the applicator (for applying cosmetics, for pine surge, etc.) , taking into consideration the amount of cosmetics contained, etc., and determining the amount so as to provide a good texture.
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ãšãããšè¯å¥œã§ããã If the amount of spherical beads added is large, foaming may become difficult. In such cases, the foaming raw material and foaming conditions are controlled. In normal cases, spherical beads can be blended in an amount of about 5 to 70% by weight based on the solid content of the foaming raw material. However, in consideration of the strength of the obtained foam, it is preferable to set the amount to about 50% of the weight of the foaming raw material.
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ããªãŒã ã·ãŒãïŒçºæ³¡åçïŒ40åïŒãçšãããExample 2 As the sheet-like foam 12, polyurethane SD
A 7 mm thick foam sheet (expansion ratio: 40 times) from Bridgestone Tire Co., Ltd. was used.
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å100éééšã«å¯Ÿã50éééšã®å²åã§æ·»å ããæš¹
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ã«çºæ³¡ãããããå¡åžæ¶²ãšããã A foam stabilizer, a thickener, and a crosslinking agent were added to the polyurethane emulsion in the same manner as in Example 1, and nylon spherical beads with an average particle size of 10 ÎŒm were added at a ratio of 50 parts by weight to 100 parts by weight of polyurethane solids. A resin liquid was prepared, and air was blown into the resin liquid to foam it four times, and this was used as a coating liquid.
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ãã€ããªãŒããŒããŒã«ã³ãŒã¿ãŒã§0.8mmã®åãã«
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ãã After applying this coating solution to the surface of the sheet-like foam 12 to a thickness of 0.8 mm using a knife-over roll coater, a release sheet made of polyester nonwoven fabric was immediately adhered to the surface in the same manner as in Example 1, and a temperature of 20°C at 80°C was applied. After drying for 10 minutes, heat treatment was performed at 140°C for 10 minutes to crosslink the components of the coating liquid and solidify them in a foamed state. Then, after the sheet obtained in this way had cooled, the adhered nonwoven fabric was peeled off. Polyurethane sheet 12
An applicator material 1 provided with a foam layer 13' having fine fluff-like naps 31 and spherical beads 32 on the surface of the applicator material 1.
I got it. This applicator material 1 was finished by punching or the like to produce a puff for powder leaf foundation.
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ãŠè¯å¥œã§ããã The puff of this example has a good feel because the fluffy naps 31 are present on the coated surface, and the spherical beads 32 are arranged on the surface of the foam skeleton of the foam layer 13' (including the fuzzy naps 31). Since the part is exposed, the sensation of irritation is further reduced and the feel is extremely good. Furthermore, when applying powdered cosmetics, etc., the powder content is extremely good compared to conventional products of this type.
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åããŠãããã Furthermore, in addition to blending spherical beads into the foaming raw material liquid as in Example 2, other materials for improving the properties and texture (touch) of cosmetics are also blended into the foaming raw material liquid. Good too.
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èœã§ããã For example, when adding hygroscopicity to a foam and using it as an applicator for summer cosmetics, as a modifying material,
For water absorption and water retention properties of cross-linked polymers of carboxymethyl cellulose, alkali metal carboxylate salts, starch-acrylic polymers, vinylon, rayon, acrylic moisture absorption materials, sponge powder, cotton powder, calcium carbonate, calcium sulfate, polyamino acids, etc. It is possible to blend excellent powders and fibers.
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ç¶æ¹è³ªæã®æ¹ã倧ããå Žåã¯ããã®æ§ãªåŸåãã
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ãŸã§ãé床ãšãããšããã Furthermore, when used for oil-based foundations, it can be modified by adding silicone resin, silicone oil as a lipophilic material, or fluororesin as an oil repellent agent. In the case of a powdery modifier, it is preferable that its size is the same as or smaller than the spherical beads 32. Also, spherical beads 3
If the mixing ratio with 2 is too large, the smooth texture of the spherical beads 32 cannot be fully utilized. Particularly, when the granular modifier is larger, there is such a tendency, so the amount of the modifier should be limited to about the same amount as the spherical beads 32.
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ããããªãã¡ãç²åŸãæè³ªã®ç°ãªã€ãçç¶ããŒãº
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ããã Furthermore, when adding spherical beads, it is also possible to mix a plurality of beads with different sizes. That is, by incorporating spherical beads of different particle sizes and materials into a foam that takes into consideration the viscosity, properties, etc. of the make-up cosmetic, it is possible to obtain a cosmetic applicator with even better absorption of the cosmetic. can.
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The cosmetic applicator of the present invention has a foam layer on the surface of the applicator body with a foaming ratio smaller than that of the applicator body, and the outer surface of this foam layer serves as the cosmetic application surface, so it has a good feel. Moreover, since this cosmetic application surface has ultra-fine fluff-like raised hairs, according to the cosmetic applicator of the present invention, the fluff-like raised hairs come into contact with the skin during application of the cosmetic, causing non-irritation and Soft touch and does not irritate the skin.
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ã§ãå¡åžæã«èãåºæ¿ããªãã Furthermore, even if the foam skeleton on the surface of the applicator body has sharp cut edges caused by processing such as polishing or cutting, these cut edges are covered with the foam layer, so they do not irritate the skin during application.
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ç£å¹çãè¯å¥œã§ããã Conventional applicators made of foam required a step of polishing the cosmetic application surface, but according to the present invention, a foam layer having fine fluff-like naps is formed on the surface of the applicator body made of foam. Since this is provided, there is no need for a polishing process for the cosmetic-applied surface, resulting in good production efficiency.
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çºæ³¡ã®è¡šé¢èã¯å¥é¢çšã·ãŒããå¥é¢ãããšãã«ã
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ããç°¡åãªçç£å·¥çšãšãªãã In addition, if a foam with a small expansion ratio is simply applied to completely cover the surface of the applicator body,
A non-foaming surface film is formed on the coated surface. However, according to the present invention, since the release sheet is peeled off while tearing the foam layer, the non-foamed surface film of the foam layer is removed when the release sheet is peeled off.
Since the surface film is peeled off at the same time, there is no need to remove the surface film using a knife or polishing as in the conventional method.Therefore, there is no need to process the polishing debris generated when the surface film is removed, resulting in a simple production process.
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ç®èãžã®åºæ¿ãéåžžã«å°ããã In the cosmetic applicator of the present invention, when spherical beads are included in the foam layer, the spherical beads come into contact with the skin during application because they are deposited on the surface of the skeleton forming the foam layer. Spherical beads have round surfaces and no sharp edges, so they do not give a tingling or stiff feeling when they come into contact with the skin, and are extremely less irritating to the skin. Moreover, since the spherical beads are in point contact with the skin when applying the cosmetic, the contact area between the skin and the foam skeleton is small, and therefore the frictional resistance when spreading the cosmetic is small.
Very little irritation to the skin.
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FIG. 1 is a sectional view showing one embodiment of the cosmetic applicator of the present invention, FIG. 2 is a sectional view showing another embodiment of the cosmetic applicator of the present invention, and FIGS. 3 and 4 are respectively FIG. 7 is a perspective view showing yet another embodiment. 5A to 5F are cross-sectional views of the applicator material at each step for explaining the steps of manufacturing the applicator material used in the cosmetic applicator of the present invention. FIG. 6 is an enlarged sectional view schematically showing the surface of the foam layer on the sheet-like foam after the release sheet has been peeled off. FIG. 7 is a sectional view showing another embodiment of the applicator material of the present invention, FIG. 8 is a sectional view showing still another embodiment of the applicator material of the present invention, and FIG. 9 is a sectional view showing another embodiment of the applicator material of the present invention. FIG. 7 is a cross-sectional view showing still another example of the material (having a foam layer containing spherical beads). 1... Applicator material, 2... Applicator body, 3...
Foam layer, 4... Release sheet, 5... Canopy, 6...
... adhesive, 7 ... core, 8 ... pattern, 9 ... core, 10 ... anchor coat layer, 12 ... sheet-like foam, 13 ... coating layer, 13' ... foam layer,
31...Fuzzy raised, 32...Spherical beads.
Claims (1)
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å ·ã®è£œé æ¹æ³ã[Scope of Claims] 1. An applicator body made of foam, and a foam layer coated on the surface of the body and having a smaller foaming ratio than the body, and the foam layer has fine particles formed by tearing on its outer surface. 1. A cosmetic applicator having a fluff-like nap, the outer surface having the fluff-like nap serving as a cosmetic application surface. 2. The cosmetic applicator according to claim 1, wherein spherical beads are mixed in the foam layer. 3 Consists of an applicator main body made of foam, an anchor coat layer applied to the surface of the main body, and a foam layer applied to the surface of the anchor coat layer and having a smaller foaming ratio than the main body, and the foam layer is 1. A cosmetic applicator, characterized in that the outer surface has fine fluff-like naps produced by tearing, and the outer surface with the fluff-like naps serves as a cosmetic application surface. 4. The cosmetic applicator according to claim 3, wherein the anchor coat layer is a liquid-impermeable layer. 5. The foaming raw material liquid is mechanically foamed or brought into a state where it can be foamed by mixing a foaming agent or by a chemical reaction, and the foaming raw material liquid is separated from a sheet-like foam made of a foam having a foaming ratio larger than the foaming ratio of the foaming raw material liquid. The foaming material liquid is brought into a foamed state and at least substantially solidified to form a foamed layer.Then, the peeling sheet is peeled off while tearing the foamed layer, and the foaming material liquid is foamed. 1. A method for manufacturing a cosmetic applicator, characterized in that the body serves as an applicator main body, and the foam layer formed on the surface of the sheet-like foam serves as a cosmetic application surface.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12625686A JPS62284606A (en) | 1986-05-31 | 1986-05-31 | Pplicator for cosmetics and its production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12625686A JPS62284606A (en) | 1986-05-31 | 1986-05-31 | Pplicator for cosmetics and its production |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62284606A JPS62284606A (en) | 1987-12-10 |
| JPH0415681B2 true JPH0415681B2 (en) | 1992-03-18 |
Family
ID=14930674
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12625686A Granted JPS62284606A (en) | 1986-05-31 | 1986-05-31 | Pplicator for cosmetics and its production |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62284606A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008029820A (en) * | 2006-07-07 | 2008-02-14 | Nishikawa Rubber Co Ltd | Method for producing a cosmetic sponge puff |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5152661B2 (en) * | 2008-08-22 | 2013-02-27 | æ ªåŒäŒç€Ÿç«¹å®å | Tip with face shaft |
| JP5105546B2 (en) * | 2008-09-05 | 2012-12-26 | äžåŸå·¥æ¥æ ªåŒäŒç€Ÿ | Makeup brush |
| US9498043B2 (en) * | 2012-03-06 | 2016-11-22 | Taiki Corp., Ltd. | Cosmetics applicator |
| KR102587332B1 (en) * | 2015-03-17 | 2023-10-12 | (죌)ì몚ë íŒìíœ | Applicator of cosmetic composition containing impermeable layer |
| JP2020005684A (en) * | 2018-07-03 | 2020-01-16 | éªã¶è°·ååŠå·¥æ¥æ ªåŒäŒç€Ÿ | Cosmetic puff and manufacturing method therefor |
-
1986
- 1986-05-31 JP JP12625686A patent/JPS62284606A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008029820A (en) * | 2006-07-07 | 2008-02-14 | Nishikawa Rubber Co Ltd | Method for producing a cosmetic sponge puff |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62284606A (en) | 1987-12-10 |
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