JPS63246103A - Material for cosmetics application and its production - Google Patents
Material for cosmetics application and its productionInfo
- Publication number
- JPS63246103A JPS63246103A JP8040087A JP8040087A JPS63246103A JP S63246103 A JPS63246103 A JP S63246103A JP 8040087 A JP8040087 A JP 8040087A JP 8040087 A JP8040087 A JP 8040087A JP S63246103 A JPS63246103 A JP S63246103A
- Authority
- JP
- Japan
- Prior art keywords
- foam
- water
- rubber latex
- weight
- parts
- 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.)
- Granted
Links
- 239000002537 cosmetic Substances 0.000 title claims description 69
- 239000000463 material Substances 0.000 title claims description 32
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000006260 foam Substances 0.000 claims description 65
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 65
- 229920000126 latex Polymers 0.000 claims description 34
- 239000007864 aqueous solution Substances 0.000 claims description 29
- 239000010419 fine particle Substances 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 21
- 239000000835 fiber Substances 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 18
- 239000000843 powder Substances 0.000 claims description 17
- 239000011148 porous material Substances 0.000 claims description 14
- 238000005187 foaming Methods 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 238000010828 elution Methods 0.000 claims description 7
- 239000004088 foaming agent Substances 0.000 claims description 4
- 239000011859 microparticle Substances 0.000 claims description 2
- 238000004073 vulcanization Methods 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 229920002261 Corn starch Polymers 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000008120 corn starch Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 230000009471 action Effects 0.000 description 6
- 229920001821 foam rubber Polymers 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 102000013142 Amylases Human genes 0.000 description 5
- 108010065511 Amylases Proteins 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000004816 latex Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- 235000014692 zinc oxide Nutrition 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 230000003712 anti-aging effect Effects 0.000 description 4
- 230000035597 cooling sensation Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 229940096992 potassium oleate Drugs 0.000 description 4
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 4
- 238000004080 punching Methods 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- 229920000858 Cyclodextrin Polymers 0.000 description 3
- 229920005830 Polyurethane Foam Polymers 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 229940111205 diastase Drugs 0.000 description 3
- -1 etc.) Natural products 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920006173 natural rubber latex Polymers 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000011496 polyurethane foam Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 2
- 239000004382 Amylase Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- 239000004375 Dextrin Substances 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 235000019418 amylase Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 235000019425 dextrin Nutrition 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000006261 foam material Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001592 potato starch Polymers 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LFMQNMXVVXHZCC-UHFFFAOYSA-N 1,3-benzothiazol-2-yl n,n-diethylcarbamodithioate Chemical compound C1=CC=C2SC(SC(=S)N(CC)CC)=NC2=C1 LFMQNMXVVXHZCC-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 244000017020 Ipomoea batatas Species 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- FVFJGQJXAWCHIE-UHFFFAOYSA-N [4-(bromomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CBr)C=C1 FVFJGQJXAWCHIE-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229940088990 ammonium stearate Drugs 0.000 description 1
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000013518 molded foam Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 229940114926 stearate Drugs 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は化粧用塗布具素材およびその製造方法、詳しく
は、特に水に濡らして水性メイクアップ化粧料を塗布す
るのに適し、しかも、乾燥したままで化粧料を塗布する
のにも適した化粧用塗布具のための多孔質素材およびそ
の製造方法に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a cosmetic applicator material and a method for manufacturing the same. The present invention relates to a porous material for a cosmetic applicator suitable for applying cosmetics while the product is in use, and a method for manufacturing the same.
(従来の技術〕
粉末固型状の水性メイクアップ化粧料が従来から多用さ
れている。(Prior Art) Water-based makeup cosmetics in the form of solid powder have been widely used.
水性メイクアップ化粧料は粉末固型状で、水で化粧料を
溶いて塗布するものであり、すなわち、水分を含浸させ
た多孔質体に化粧料を付着させた後、この多孔質体によ
り化粧料を肌に塗布するものである。水を使用するため
清涼感が得られ、夏場の化粧料として従来から用いられ
ている。Water-based makeup cosmetics are in the form of a solid powder and are applied by dissolving the cosmetics in water.In other words, after the cosmetics are attached to a porous body impregnated with water, the porous body is used to apply makeup. The substance is applied to the skin. Because it uses water, it provides a refreshing feeling and has traditionally been used as a summer cosmetic.
また、最近では、水あり水なしの両用タイプのメイクア
ップ化粧料(すなわち、水性メイクアップ化粧料と同様
に水で塗布具を濡らしてから化粧料を付着して塗布する
ことも、或は、塗布具を濡らさずに乾燥したままで化粧
料を付着して塗布することもできるタイプの化粧料)が
使い易く便利であるため、消費者に好まれており、夏場
の化粧ねとして多用されている。In addition, recently, makeup cosmetics that can be used with or without water (i.e., similar to water-based makeup cosmetics, wet the applicator with water and then apply the cosmetic by adhering to it, or This type of cosmetic (which allows you to apply the cosmetic while it is dry without getting the applicator wet) is easy to use and convenient, so it is preferred by consumers and is often used as a makeup base in the summer. There is.
水性メイクアップ化粧料用の塗布具素材としては、天然
海綿、ポリウレタン発泡体、ゴムラテックス発泡体、ポ
リビニルアルコール系発泡体等の各種発泡体、不織布等
の多孔質素材が従来から多用されている。As applicator materials for aqueous makeup cosmetics, various foams such as natural sponge, polyurethane foam, rubber latex foam, and polyvinyl alcohol foam, and porous materials such as nonwoven fabrics have been widely used.
水あり水なしの両用タイプのメイクアップ化粧料用塗布
具素材としては、乾燥状態でも柔軟であることが必要で
あるので、ポリウレタン発泡体、ゴムラテックス発泡体
等の各種発泡体、不織布等の多孔質素材が用いられてい
る。Materials for makeup cosmetic applicators that can be used with or without water need to be flexible even in dry conditions, so various foams such as polyurethane foam and rubber latex foam, and porous materials such as non-woven fabrics are used. Quality materials are used.
夏期の化粧に用いる化粧料や化粧用塗布具には、使用時
に冷感を伴うことが、強く求められている。There is a strong demand for cosmetics and cosmetic applicators used for summer makeup to provide a cooling sensation when used.
天然海綿やポリビニルアルコール系発泡体は濡らした状
態では柔軟で冷感があるので、水性メイクアップ化粧料
の塗布には好まれて使用されている。しかしながら、天
然海綿はコストが割高であり、しかも、乾燥状態ではゴ
ワゴワするので水あり水なしの両用タイプの化粧料の塗
布具としては不適当である。また、ポリビニルアルコー
ル系発泡体は濡れた状態では柔軟であるが、乾燥状態で
はカチン力チンに硬くなってしまうので、水あり水なし
の両用タイプの化粧料の塗布具としては不適当である。Natural sponges and polyvinyl alcohol foams are flexible and have a cool feel when wet, so they are preferred for use in applying water-based makeup cosmetics. However, natural sponge is expensive and, furthermore, is stiff when dry, making it unsuitable for use as a dual-use cosmetic applicator that can be used with or without water. Further, although polyvinyl alcohol foam is flexible when wet, it becomes extremely hard when dry, making it unsuitable as a dual-use cosmetic applicator for use with or without water.
しかも、乾燥状態から再び水で濡らす場合、発泡体の中
まで水が浸透するのに時間が掛かるという問題もある。Moreover, when rewetting the foam from a dry state, there is a problem in that it takes time for the water to penetrate into the foam.
一方、ポリウレタン発泡体やゴムラテックス発泡体は乾
燥状態でも柔軟であるので、水あり水なしの両用タイプ
のメイクアップ化粧料用塗布具として適している。しか
しながら、水を用いて塗布を行っても、皮膚に接触する
時の感じが冷感に乏しいという問題がある。On the other hand, polyurethane foam and rubber latex foam are flexible even in a dry state, so they are suitable as a dual-use makeup cosmetic applicator that can be used with or without water. However, even when applied using water, there is a problem in that the skin does not feel cool when it comes in contact with the skin.
本発明はこのような従来の問題を解決し、水性メイクア
ップ化粧料の塗布時において、使用する塗布具から冷感
を得ながら、爽かに化粧料を塗布でき、しかも、乾燥状
態でも柔軟で、水あり水なしの両用タイプの化粧料の塗
布にも適している化粧用塗布具用の多孔質素材およびそ
の製造方法を提供することを目的とする。The present invention solves these conventional problems, and when applying water-based makeup cosmetics, it is possible to apply the cosmetics refreshingly while getting a cooling sensation from the applicator used, and moreover, it is flexible even in dry conditions. It is an object of the present invention to provide a porous material for a cosmetic applicator that is suitable for application of dual-use cosmetics with and without water, and a method for manufacturing the same.
本発明は上述の問題を、通気性を有し且つ乾燥状態でも
柔軟な、ゴムラテックスを主成分とじた発泡体であり、
該発泡体は気泡により形成された小孔の他に、水または
水溶液に溶解可能な微粒子の溶出により形成された微細
孔を有している化粧用塗布具素材によって解決した。The present invention solves the above-mentioned problems by providing a foam mainly composed of rubber latex, which is breathable and flexible even in a dry state.
The foam was solved by a cosmetic applicator material having, in addition to small pores formed by air bubbles, micropores formed by the elution of fine particles soluble in water or an aqueous solution.
更に、本発明によれば、上記化粧用塗布具素材の製造方
法として、水または水溶液に溶解可能な微粒子をゴムラ
テックスを主成分とする液中に混入配合し、該混合液に
気体を吹込むかまたは発泡剤を混合し、泡立ち状態で凝
固させ、加硫して、ゴムラテックス発泡体を形成し、該
ゴムラテックス発泡体を水または水溶液で洗浄して、ゴ
ムラテックス発泡体から前記微粒子を溶出させて微細孔
を形成することを特徴とする化粧用塗布具素材の製造方
法が提供される。Furthermore, according to the present invention, as a method for manufacturing the cosmetic applicator material, fine particles soluble in water or an aqueous solution are mixed and blended into a liquid mainly composed of rubber latex, and a gas is blown into the mixed liquid. Alternatively, a blowing agent is mixed, solidified in a foamy state, and vulcanized to form a rubber latex foam, and the rubber latex foam is washed with water or an aqueous solution to elute the fine particles from the rubber latex foam. Provided is a method for producing a material for a cosmetic applicator, which is characterized by forming micropores.
〔作 用〕
本発明の化粧用塗布具素材においては、ゴムラテックス
発泡体全体に気泡によって形成された小孔および微粒子
の溶出により形成された微細孔が存在する。このように
、化粧料塗布素材全体に小孔および微細孔があるため、
本発明の素材を用いた化粧用塗布具は水に濡らした際、
微細孔により毛細管現象が生じ、水が微細孔を伝わって
化粧料塗布表面に揚がり、化粧料塗布表面を常に濡れた
状態とする。しかも、この表面が微細な凹凸構造であり
、且つ通気性、透水性を有するため、水が蒸発し易く、
水の蒸発により化粧料塗布表面が冷却され、従って、塗
布時に清涼感を与える。[Function] In the cosmetic applicator material of the present invention, small pores formed by air bubbles and micropores formed by elution of fine particles are present throughout the rubber latex foam. In this way, since there are small and micropores throughout the cosmetic application material,
When the cosmetic applicator using the material of the present invention gets wet with water,
Capillary action occurs due to the micropores, and water travels through the micropores and rises to the surface on which the cosmetic is applied, keeping the surface on which the cosmetic is applied always wet. Moreover, since this surface has a fine uneven structure and has breathability and water permeability, water easily evaporates.
The evaporation of water cools the cosmetic application surface, thus providing a cooling sensation upon application.
また、化粧料塗布具全体に小孔および微細孔があるため
、化粧用塗布具を水に濡らした際の保水量が増加する。Furthermore, since the entire cosmetic applicator has small pores and micropores, the amount of water retained when the cosmetic applicator is wetted with water is increased.
更に、塗布具素材はゴムラテックス発泡体であり、乾燥
状態でも柔軟であるので、水あり水なしの両用タイプの
化粧料の塗布にも使用できる。Furthermore, since the material of the applicator is rubber latex foam and is flexible even in a dry state, it can be used to apply both water- and water-less cosmetics.
本発明の化粧用塗布具素材は、通気性を有し且つ乾燥状
態でも柔軟な、ゴムラテックスを主成分とする発泡体で
あり、該発泡体は気泡により形成された小孔の他に、水
または水溶液に溶解可能な微粒子の溶出により微細孔が
形成されているものである。The cosmetic applicator material of the present invention is a foam mainly composed of rubber latex, which is breathable and flexible even in a dry state. Alternatively, micropores are formed by elution of microparticles that can be dissolved in an aqueous solution.
前記水溶液は、酸性水溶液またはアルカリ性水溶液でも
よく、或は酸化剤または還元剤を含む水溶液でもよい。The aqueous solution may be an acidic aqueous solution or an alkaline aqueous solution, or an aqueous solution containing an oxidizing agent or a reducing agent.
また、澱粉等の微粒子の溶解にはジアスターゼ、アミラ
ーゼ等の酵素を含む水溶液を用いてもよい。Furthermore, an aqueous solution containing enzymes such as diastase and amylase may be used to dissolve fine particles such as starch.
ゴムラテックスとしては、天然ゴムラテックスでも、N
BRラテックス、SBRラテックス等の合成ゴムラテッ
クスでも用いることができる。As rubber latex, even natural rubber latex, N
Synthetic rubber latex such as BR latex and SBR latex can also be used.
ゴムラテックス発泡体に混入される、水または水溶液に
溶解可能な微粒子としては、澱粉、デキストリン、高級
アルコール(例えば、オレイルアルコール、ステアリル
アルコール、ペンタエリスリトール、ポリプロピレング
リコール、ポリエチレングリコール等)、脂肪酸く例え
ば、ステアリン酸、オレイン酸等)、炭酸カルシウム等
の微粒子を用いればよい。Fine particles that can be dissolved in water or an aqueous solution to be mixed into the rubber latex foam include starch, dextrin, higher alcohols (for example, oleyl alcohol, stearyl alcohol, pentaerythritol, polypropylene glycol, polyethylene glycol, etc.), fatty acids, etc. Fine particles of stearic acid, oleic acid, etc.), calcium carbonate, etc. may be used.
微粒子の大きさく粒径)は、微粒子が溶出して形成され
た微細孔が毛細管現象により、化粧料塗布表面を濡れた
状態とすることができる程度のものとする。The size of the fine particles (particle diameter) is such that the fine pores formed by the elution of the fine particles can moisten the surface to which the cosmetic is applied due to capillary action.
馬鈴薯澱粉、とうもろこし澱粉、さつまいも澱粉等の粒
子径は一般に、1〜200ミクロン程度であるが、発泡
体の骨格より〜も微粒子が小さい方が好ましい。微粒子
が発泡骨格よりも大きいと発泡骨格が破れてしまい、発
泡安定性が悪くなり、良好な発泡体とならず、また、毛
細管現象も減少してしまう。従って、粒子径は100ミ
クロン以下、好ましくは、50ミクロン以下とする。The particle size of potato starch, corn starch, sweet potato starch, etc. is generally about 1 to 200 microns, but it is preferable that the fine particles are smaller than the skeleton of the foam. If the fine particles are larger than the foamed skeleton, the foamed skeleton will be torn, resulting in poor foaming stability, resulting in poor foaming, and also reducing capillary action. Therefore, the particle size should be 100 microns or less, preferably 50 microns or less.
また、粒子径が小さ過ぎると、発泡体に混入されていた
微粒子の量が少ない場合には、毛細管現象により塗布具
表面に揚がる水の量が充分でないことがあるので、粒子
径は1ミクロン程度までとすることが好ましい。In addition, if the particle size is too small and the amount of fine particles mixed in the foam is small, the amount of water that rises to the surface of the applicator due to capillary action may not be sufficient, so the particle size should be approximately 1 micron. It is preferable to keep it up to.
本発明の化粧用塗布具素材を製造するには、先ず、発泡
体を形成するためのゴムラテックスを主成分とする発泡
原料液に、架橋剤または加硫剤、泡安定剤および無機ま
たは有機の微粒子を混合する。To produce the cosmetic applicator material of the present invention, first, a foaming raw material liquid containing rubber latex as a main component to form a foam is added with a crosslinking agent or vulcanizing agent, a foam stabilizer, and an inorganic or organic Mix the particulates.
発泡体を形成する原料と微粒子の混合比は、微粒子が少
な過ぎると毛細管現象による濡れ効果が小さく、多過ぎ
ると発泡体の強度が低下したり、発泡時の粘度が非常に
高くなり過ぎて発泡できなくなる。従って、ゴムの固型
分100重量部に対して、微粒子5〜100重量部、好
ましくは5〜30重量部とするとよい。The mixing ratio of the raw materials forming the foam and the fine particles is such that if there are too few fine particles, the wetting effect due to capillary action will be small, and if there are too many, the strength of the foam will decrease or the viscosity during foaming will become too high, causing foaming. become unable. Therefore, the fine particles should be used in an amount of 5 to 100 parts by weight, preferably 5 to 30 parts by weight, per 100 parts by weight of the solid content of the rubber.
ゴムラテックスの架橋剤としては、硫黄または含硫黄加
硫剤、加硫促進剤等を用いればよい。As a crosslinking agent for rubber latex, sulfur or a sulfur-containing vulcanizing agent, a vulcanization accelerator, etc. may be used.
泡安定剤としては、オレイン酸カリ、ステアリン酸カリ
、ステアリン酸アンモン、オレイン酸アンモン等を用い
ればよい。As the foam stabilizer, potassium oleate, potassium stearate, ammonium stearate, ammonium oleate, etc. may be used.
オークスミキサ等の連続気泡装置で混合液に空気または
他のガスを吹込むか、或は発泡剤を混合して、3〜5倍
に発泡させる。Air or other gas is blown into the mixed liquid using an open-cell device such as an oak mixer, or a blowing agent is mixed therein to foam the mixture three to five times.
発泡剤としては、例えばフレオン、ブタン、プロパン等
の低沸点の液体等のガス発生物質を用いることができる
。As the blowing agent, gas generating substances such as low boiling point liquids such as freon, butane, propane, etc. can be used.
次に、前述のように発泡させた混合液を連続気泡装置か
ら吐出し、任意の注型体に入れて凝固させ、加熱または
蒸熱して加硫し、注型体から取出す。Next, the foamed mixture as described above is discharged from the open cell device, put into an arbitrary cast body, solidified, heated or steamed to vulcanize, and taken out from the cast body.
この発泡体をスライス、打扱き等した後、この成形した
発泡体を水(冷水、温湯いずれも可)または水溶液中で
洗浄し、発泡体に含まれている前記微粒子および泡安定
剤の一部を溶出させて、発泡体に微細孔を形成する。After slicing, punching, etc., this foam is washed in water (cold water or hot water is acceptable) or an aqueous solution to remove some of the fine particles and foam stabilizer contained in the foam. is eluted to form micropores in the foam.
なお、上記上述の場合は化粧用塗布具の形状に成形して
から、澱粉、デキストリン、高級アルコール等の微粒子
の溶出を行ったが、発泡体がシート状の場合は、微粒子
の溶出を行ってから、打抜き加工等により化粧用塗布具
として仕上げてもよい。In addition, in the case described above, fine particles such as starch, dextrin, and higher alcohols were eluted after being formed into the shape of a cosmetic applicator, but when the foam was in the form of a sheet, fine particles were eluted. It may also be finished as a cosmetic applicator by punching or the like.
本発明の化粧用塗布具素材の別の実施例によれば、前述
した実施例と同様に、通気性を有し且つ乾燥状態でも柔
軟なゴムラテックス発泡体からなる塗布具素材は、前述
した実施例と同様に、気泡により形成された小孔および
水または水溶液に溶解可能な微粒子の溶出により形成さ
れた微細孔を有しており、更に、前記発泡体中にtan
粉末を含んでいる。According to another embodiment of the cosmetic applicator material of the present invention, similar to the previous embodiment, the applicator material is made of a rubber latex foam that is breathable and flexible even in a dry state. Similarly to the example, the foam has small pores formed by air bubbles and micropores formed by elution of fine particles soluble in water or an aqueous solution, and furthermore, the foam has tan
Contains powder.
このように発泡体に繊維粉末を混入することにより、感
触が良好となり、しかも、より一層優れた吸水性および
水に濡れた場合の冷却効果を得ることができる。By mixing the fiber powder into the foam in this way, it has a good feel, and furthermore, it is possible to obtain even better water absorbency and a cooling effect when wet with water.
前記m雑粉末としては、綿、ビスコースレイヨン、キュ
プラ、麻、亜麻、紙、バルブ等のセルロース繊維;海綿
、羊毛、獣毛、天然皮革の粉砕物等の蛋白質繊維;およ
びナイロン、ポリエステル、アクリル!lH等の合成m
雑を微細に粉砕したものを用いることができる。好まし
くは、セルロース4I緒や蛋白質繊維のような親水性繊
維を用いるとよい。また、合成timlの場合は、細デ
ニールの繊維粉砕物とするとよい。The miscellaneous powders include cellulose fibers such as cotton, viscose rayon, cupro, hemp, flax, paper, and bulbs; protein fibers such as crushed products of sponge, wool, animal hair, and natural leather; and nylon, polyester, and acrylic. ! Synthesis of lH etc.
It is possible to use finely pulverized material. Preferably, hydrophilic fibers such as cellulose 4I fibers and protein fibers are used. In addition, in the case of synthetic TIML, it is preferable to use a fine denier pulverized fiber.
繊維粉末は余り大きいと発泡体に悪影響が生じるので、
20メツシュ程度のふるいを通過するものを用いる。好
ましくは、50メツシユのふるいを通過するものを用い
ると良い。If the fiber powder is too large, it will have a negative effect on the foam, so
Use a material that can pass through a sieve of about 20 mesh. Preferably, one that passes through a 50-mesh sieve is used.
繊維粉末に用いるm維の太さは、15デニール以下、好
ましくは5デニール以下とする。合成繊維では感触を良
好にするには、1デニール以下とするとよい。特に、合
成I!雑の内、ナイロンやポリエステル等からなり、再
分割!l維や海島繊維のように、0.005〜0.2デ
ニールのような超極細デニールの繊維とすると、非常に
良好な感触が得られる。The thickness of the m fibers used in the fiber powder is 15 deniers or less, preferably 5 deniers or less. For synthetic fibers, the denier should be 1 denier or less to provide a good feel. In particular, Synthesis I! Of the miscellaneous items, it consists of nylon, polyester, etc., and is redivided! If the fiber is made of ultrafine denier, such as 0.005 to 0.2 denier, such as l fiber or sea-island fiber, a very good feel can be obtained.
m維粉末入り発泡体を形成するには、発泡体を形成する
ためのゴムラテックスに、加硫剤、泡安定剤および無機
または有機の微粒子を混合する際に、繊維粉末も一緒に
混入すればよい、m維粉末の混合割合は、発泡原料液の
固型分に対して、1〜40重世%であるが、好ましくは
、3〜15重量%程度である。上記好ましい範囲にする
と、より゛一層良好な感触が得られる。To form a foam containing fiber powder, when mixing a vulcanizing agent, a foam stabilizer, and inorganic or organic fine particles with the rubber latex for forming the foam, the fiber powder is also mixed. A good mixing ratio of the m-fiber powder is 1 to 40 weight percent, preferably about 3 to 15 weight percent, based on the solid content of the foaming raw material liquid. When the above-mentioned preferred range is set, an even better feeling can be obtained.
繊維粉末を混入した場合も、その後は前述した実施例と
同様に処理して、化粧用塗布具素材を製造することがで
きる。すなわち、オークスミキサ等の連続気泡vt置で
混合液に空気または他のガスを吹込むか、或は発泡剤を
混合して、3〜5倍に発泡させる。前述のように発泡さ
せた混合液を連続気泡装置から吐出し、任意の注型体に
入れて凝固させ、加熱または蒸熱して加硫し、注型体か
ら取出す。この取出した発泡体をスライス、打抜き等し
た後、この成形した発泡体を、水または水溶液(酸性水
溶液、アルカリ性水溶液、酸化剤を含む水溶液または還
元剤を含む水溶液)中で洗浄し、発泡体に含まれている
前記微粒子および泡安定剤の一部を溶出させて、発泡体
に微細孔を形成する。Even when fiber powder is mixed, the cosmetic applicator material can be manufactured by processing in the same manner as in the above-described embodiment. That is, air or other gas is blown into the mixed liquid in an open-cell VT device such as an oak mixer, or a foaming agent is mixed therein to foam the mixture to a size of 3 to 5 times. The foamed mixture as described above is discharged from the open cell device, poured into an arbitrary cast body, solidified, heated or steamed to vulcanize, and taken out from the cast body. After slicing, punching, etc. the taken out foam, the molded foam is washed in water or an aqueous solution (acidic aqueous solution, alkaline aqueous solution, aqueous solution containing an oxidizing agent or aqueous solution containing a reducing agent), and then A portion of the fine particles and foam stabilizer contained therein are eluted to form micropores in the foam.
このようにして出来上がった発泡体を有する多孔質素材
を打抜き、成形等の加工を施して、化粧用塗布具として
仕上げる。The porous material having the foam thus produced is punched out, processed by molding, etc., and finished as a cosmetic applicator.
(実施例1)
NBRラテックスのN1pol LX−511・・・
200重量部、亜鉛華と硫黄とを3:1の割合で混合し
たちの30部を水70部で乳化した30%水分散体・・
・18重量部、加硫促進剤MZ・・・4重量部、加硫促
進剤EZ・・・5重量部、老化防止剤SP・・・1.8
重量部、トリメンベース・・・1.5重量部、エマルゲ
ン920(第一工業株式会社の製品)・・・1.3重量
部からなる配合物Aに:とうもろこし澱粉・・・35重
量部、水・・・60重量部、ケイ弗化ソーダ・・・10
重」部からなる配合物Bをオークスミキサ−を用いて配
合物Aを100重山部に対して配合物Bを35重量部の
割合で注入しつつ、約4倍に発泡させながら吐出し、円
筒形に注型凝固させた。(Example 1) N1pol LX-511 of NBR latex...
A 30% aqueous dispersion made by emulsifying 200 parts by weight of zinc white and sulfur in a ratio of 3:1 with 70 parts of water.
・18 parts by weight, vulcanization accelerator MZ...4 parts by weight, vulcanization accelerator EZ...5 parts by weight, anti-aging agent SP...1.8
Parts by weight, trimene base...1.5 parts by weight, Emulgen 920 (a product of Dai-ichi Kogyo Co., Ltd.)...1.3 parts by weight.Formulation A: Corn starch...35 parts by weight, water. ...60 parts by weight, sodium silicofluoride...10
Using an oak mixer, Formulation B consisting of 100 parts by weight was injected at a ratio of 35 parts by weight to 100 parts by weight of Formulation A, and discharged while foaming to about 4 times the volume. Cast and solidified into shape.
更に、蒸熱ボックスにおいて102℃で30分間蒸熱油
硫させて、NBRラテックスフオームとした。Further, the product was subjected to steam oil sulfurization at 102° C. for 30 minutes in a steam box to obtain an NBR latex foam.
このラテックスフオームを5mm厚さにスライスして、
円板型パフ用素材とした。Slice this latex foam into 5mm thick pieces.
It was used as a material for disc-shaped puffs.
この素材を研削成形したのちに、苛性ソーダの0.05
%水溶液(40℃)に24時間浸漬し、その後、攪拌、
洗浄、脱水を2回繰返して、とうもろこし澱粉を溶出さ
せてから脱水乾燥した。After grinding and forming this material, 0.05% of caustic soda
% aqueous solution (40°C) for 24 hours, then stirred,
Washing and dehydration were repeated twice to elute the corn starch, which was then dehydrated and dried.
このようにして得られたパフは吸収性、保水性が極めて
優れていた。The puff thus obtained had extremely excellent absorbency and water retention.
出来上がった製品を濡らして、標準状g(22℃、相対
湿度65%)、風速1m/秒で風に平行に設置したガラ
ス板上に置いた。そして、発泡体を形成した側の化粧用
塗布具素材表面の表面湿度を、デジタル温度計のデルタ
5K−1250(株式会社佐藤計量器製作所の製品〕に
表面接触センサーを付けたものにより測定した。The finished product was wetted and placed on a glass plate placed parallel to the wind at a standard g (22° C., 65% relative humidity) and a wind speed of 1 m/s. Then, the surface humidity of the surface of the cosmetic applicator material on the side on which the foam was formed was measured using a digital thermometer Delta 5K-1250 (manufactured by Sato Keiki Seisakusho Co., Ltd.) equipped with a surface contact sensor.
なお表面接触タイプの温度計を使用する代りに、非接触
で温度測定が可能な温度計、例えばオブティクス株式会
社製の非接触温度計THERMO−HUNTER,を用
いてもよい。この温度計は赤外線エネルギー(検出波長
7〜20μm)を非球面鏡により集光し、サーモバイル
で電気信号に変換して電気的に処理して、温度を液晶デ
ィスプレイに表示するものであり、物体の温度の移り変
りを容易に測定できる。Note that instead of using a surface contact type thermometer, a thermometer capable of non-contact temperature measurement, such as the non-contact thermometer THERMO-HUNTER manufactured by Obtics Co., Ltd., may be used. This thermometer collects infrared energy (detection wavelength: 7 to 20 μm) using an aspherical mirror, converts it into an electrical signal using a thermomobile, processes it electrically, and displays the temperature on a liquid crystal display. Changes in temperature can be easily measured.
測定結果; 3分後、表面温度は15℃に低下した。Measurement result; After 3 minutes, the surface temperature dropped to 15°C.
(比較例)
81IlIn厚さのNBRラテックスフオーム〔雪ケ谷
化学株式会社の製品〕からなる化粧用塗布具(前記のよ
うな本発明の微細孔を有していない)を用いて、上述の
測定方法により、化粧用塗布具の表面温度の変化を測定
した。(Comparative Example) The measurements described above were carried out using a cosmetic applicator made of NBR latex foam (product of Yukigaya Chemical Co., Ltd.) with a thickness of 81IlIn (without the micropores of the present invention as described above). The method measured the change in surface temperature of the cosmetic applicator.
測定結果: 3分後、表面温度は20℃であった。Measurement result: After 3 minutes, the surface temperature was 20°C.
(実施例2)
天然ゴムラテックス・・・200重量部、加硫促進剤E
Z・・・1.8重量部、加硫促進剤MZ・・・3.2重
量部、老化防止剤SP・・・2.2重量部、トリメンベ
ース・・・0.8重量部、硫黄・・・11重量部、オレ
イン酸カリ・・・8重量部、亜鉛華・・・5重量部、冷
水に不溶性のサイクロデキストリン・・・20重量部か
らなる配合物をA液とじ;
亜鉛華・・・12重量部、加硫促進剤D・・・2.1重
量部、ケイ弗化ソーダ・・・11重量部サイクロデキス
トリン・・・10重量部、ウレタンエマルジョンのスー
パーフレックス#100(第一工業製薬株式会社の製品
〕・・・55重量部からなる配合物をB液として、オー
クスミキサ−を用いてA液を100重量部に対してB液
を60重量部の割合で注入しつつ、約4倍に発泡させな
がら吐出し、円筒形に注型して放置し、凝固させながら
45分間蒸蒸熟硫して、天然ゴム/ポリウレタンの混合
ラテックスフオームとした。(Example 2) Natural rubber latex...200 parts by weight, vulcanization accelerator E
Z...1.8 parts by weight, vulcanization accelerator MZ...3.2 parts by weight, anti-aging agent SP...2.2 parts by weight, trimene base...0.8 parts by weight, sulfur... ...11 parts by weight of potassium oleate, 8 parts by weight of zinc white, 5 parts of zinc white, and 20 parts by weight of cyclodextrin insoluble in cold water.・12 parts by weight, vulcanization accelerator D...2.1 parts by weight, sodium silicofluoride...11 parts by weight cyclodextrin...10 parts by weight, urethane emulsion Superflex #100 (Daiichi Kogyo Seiyaku) Co., Ltd.'s product]...A mixture consisting of 55 parts by weight was used as liquid B, and while injecting liquid B at a ratio of 60 parts by weight to 100 parts by weight of liquid A using an oak mixer, approximately 4 parts by weight was added. The product was discharged while foaming to double its original size, cast into a cylindrical shape and left to stand, and steamed and sulfurized for 45 minutes while solidifying to form a mixed latex foam of natural rubber/polyurethane.
このラテックスフオームを7mm厚さにスライスした後
、アミラーゼとジアスターゼとを1:2の割合で混合し
た水溶液に40℃で24時間浸漬放置し、その後、攪拌
、洗浄、脱水を2回繰返してサイクロデキストリンを溶
出させてから、脱水乾燥した。After slicing this latex foam into 7 mm thick slices, it was immersed in an aqueous solution containing amylase and diastase mixed at a ratio of 1:2 at 40°C for 24 hours, and then stirring, washing, and dehydration were repeated twice to form cyclodextrin. was eluted and then dehydrated and dried.
このようにして得られたパフは吸収性、保水性が極めて
優れ、また強度的にも優れていた。更に、実施例1と同
様に水に濡らした場合、発泡体表面の冷却効果が大きか
った。The puff thus obtained had excellent absorbency and water retention, and was also excellent in strength. Furthermore, when the foam was wetted with water as in Example 1, the cooling effect on the surface of the foam was large.
(実施例3)
天然ゴムラテックス・・・15011部、SBRラテッ
クスのJSR#561 (日本合成ゴム工業株式会社の
製品)・・・100重量部、加硫促進剤EZ・・・2.
5重量部、加硫促進剤MZ・・・4重量部、老化防止剤
SP・・・2.6重量部、トリメンベース・・・2重量
部、硫黄・・・15重量部、オレイン酸カリ・・・7重
量部、とうもろこし澱粉・・・30重量部からなる配合
物をA液とし;
亜鉛華・・・16重缶部、加硫促進剤D・・・1重量部
、ケイ弗化ソーダ・・・7重量部(粉体)、Dicna
l #2575 (ポリアクリル酸エステルのエマルジ
ョン、大日本インキ化学工業株式会社の製品)・・・1
0重置部、ウレタンエマルジョンのスーパーフレックス
#100(第一工業製薬株式会社の製品〕・・・70重
量部、ステアリン酸の粉末・・・10重量部からなる配
合物をB液として、オークスミキサ−を用いてA液とB
液とを1:0.4の割合で、空気を吹込みながら、3.
5倍に発泡させつつ吐出し、正方形に角柱型に注型して
30分間放置し、凝固させた。その後、蒸熱箱の中で1
01℃で、45分間熱した後取出し、8mm厚さにスラ
イスしてゴム発泡体シートとした。これを円形に打抜い
た後、苛性ソーダ3g/l、40℃の水溶液中で攪拌、
洗浄、脱水を2回繰返してから、更に湯洗し、とうもろ
こし澱粉を溶出させて、脱水乾燥した。(Example 3) Natural rubber latex...15011 parts, SBR latex JSR#561 (product of Japan Synthetic Rubber Industry Co., Ltd.)...100 parts by weight, vulcanization accelerator EZ...2.
5 parts by weight, vulcanization accelerator MZ...4 parts by weight, anti-aging agent SP...2.6 parts by weight, trimene base...2 parts by weight, sulfur...15 parts by weight, potassium oleate... A mixture consisting of 7 parts by weight, 30 parts by weight of corn starch; 16 parts by weight of zinc white, 1 part by weight of vulcanization accelerator D, and 1 part by weight of sodium fluorosilicide. ...7 parts by weight (powder), Dicna
l #2575 (emulsion of polyacrylic acid ester, product of Dainippon Ink & Chemicals Co., Ltd.)...1
A mixture consisting of 0 parts by weight, 70 parts by weight of urethane emulsion Superflex #100 (product of Daiichi Kogyo Seiyaku Co., Ltd.), and 10 parts by weight of stearic acid powder was used as liquid B, and mixed in an oak mixer. - using liquid A and B
3. While blowing air into the liquid at a ratio of 1:0.4.
The mixture was discharged while foaming to 5 times its original size, cast into a square prism shape, and left to stand for 30 minutes to solidify. After that, 1 in a steaming box.
After heating at 0.01°C for 45 minutes, the mixture was taken out and sliced into 8 mm thick pieces to obtain rubber foam sheets. After punching this into a circular shape, it was stirred in an aqueous solution of 3 g/l of caustic soda at 40°C.
After repeating washing and dehydration twice, it was further washed with hot water to elute the corn starch, and then dehydrated and dried.
このようにして得られたパフは吸収性、保水性が極めて
優れ、また強度的にも優れていた。また、実施例1と同
様に水に濡らした場合、発泡体表面の冷却効果が大きか
った。The puff thus obtained had excellent absorbency and water retention, and was also excellent in strength. Further, when the foam was wetted with water as in Example 1, the cooling effect on the surface of the foam was large.
(実施例4)
NBRラテックス(7)NipOf LX−531(
日本ゼオン株式会社の製品)・・・100重量部、トリ
メンベース・・・0.4重量部、加硫促進剤のアクセル
EZおよびMZ(川口化学株式会社の製品〕を1=2の
割合で混ぜた混合物を50%水乳化物としたもの・・・
2重口部、老化防止剤のアンテージSP(川口化学株式
会社の製品〕の50%水乳化物・・・2重量部、硫黄の
60%水乳化物・・・7重量部、オレイン酸カリの20
%水溶液・・・3重旦部、ステアリン酸アンモ230%
水溶液・・・5重量部、とうもろこし澱粉・・・30重
量部、ポバールの5%水溶液・・・15重器部からなる
配合物Aに;亜鉛華の25%水乳化物・・・20重量部
、加硫促進剤のアクセルD〔川口化学株式会社の製品〕
の30%水乳化物・・・3重層部、ケイ弗化ソーダの2
5%水乳化物・・・10重1部、発泡剤のフレオン・・
・4重量部からなる配合物Bをオークスミキサ−を用い
て配合物Aを150重量部に対して配合物Bを20重量
部の割合で注入し、更に空気を吹込んで、約4倍に発泡
させながら吐出し、円筒形に注型し、30分間放置した
後、凝固させた。(Example 4) NBR latex (7) NipOf LX-531 (
Nippon Zeon Co., Ltd. product)...100 parts by weight, Trimenbase...0.4 part by weight, and vulcanization accelerators Accel EZ and MZ (Kawaguchi Chemical Co., Ltd. product) were mixed in a ratio of 1=2. A 50% water emulsion of the mixture...
Double mouth part, 2 parts by weight of 50% water emulsion of anti-aging agent ANTAGE SP (product of Kawaguchi Chemical Co., Ltd.), 7 parts by weight of 60% water emulsion of sulfur, 7 parts by weight of potassium oleate 20
% aqueous solution... 3x Danbe, ammo stearate 230%
Aqueous solution: 5 parts by weight, corn starch: 30 parts by weight, 5% aqueous poval solution: 15 parts by weight; 25% water emulsion of zinc white: 20 parts by weight , vulcanization accelerator Accel D [product of Kawaguchi Chemical Co., Ltd.]
30% water emulsion... 3 layers, 2 parts of sodium silicofluoride
5% water emulsion...10 parts by weight, foaming agent Freon...
・Formulation B consisting of 4 parts by weight was injected using an oak mixer at a ratio of 150 parts by weight of Formulation A and 20 parts by weight of Formulation B, and further air was blown into the foam to about 4 times the size. The mixture was discharged while stirring, cast into a cylindrical shape, and allowed to stand for 30 minutes before being solidified.
更に、102°Cで20分間加硫した後、型からはずし
て、10mI!l厚さにスライスして、円板型パフ用素
材とした。Furthermore, after vulcanizing at 102°C for 20 minutes, it was removed from the mold and heated to 10 mI! The material was sliced into l-thick pieces to obtain a disc-shaped puff material.
この素材をジアスターゼの0.1%水溶液に40℃で2
0時間浸漬放置し、90℃で湯洗して、とうもろこし澱
粉を溶出させてから、脱水乾燥した。This material was added to a 0.1% aqueous solution of diastase at 40℃ for 2 hours.
The sample was left immersed for 0 hours, washed with hot water at 90°C to elute the corn starch, and then dehydrated and dried.
このようにして得られたパフは吸収性、保水性が極めて
優れていた。また、実施例1と同様に水に濡らした場合
、発泡体表面の冷却効果が大きかった。The puff thus obtained had extremely excellent absorbency and water retention. Further, when the foam was wetted with water as in Example 1, the cooling effect on the surface of the foam was large.
本発明の化粧用塗布具素材によれば、ゴムラテックスを
主成分とした発泡体が気泡により形成された小孔および
微粒子の溶出により形成された微細孔を有しているので
、本発明の素材を用いて作った化粧用塗布具は水に濡ら
すと、微細孔により毛細管現象が生じ、水が微細孔を伝
わって化粧料塗布表面に揚がり、化粧料塗布表面を常に
濡れた状態とする。従って、塗布時には、化粧料塗布表
面より先に水が肌に接触するので、冷感が得られ、爽か
に化粧料を塗布できる。According to the cosmetic applicator material of the present invention, the foam mainly composed of rubber latex has small pores formed by air bubbles and micropores formed by elution of fine particles. When the cosmetic applicator made using the cosmetic applicator is wetted with water, capillary action occurs due to the micropores, and water travels through the micropores and rises to the surface on which the cosmetic is applied, keeping the surface on which the cosmetic is applied always wet. Therefore, when applying the cosmetic, the water comes into contact with the skin before the surface on which the cosmetic is applied, giving a cooling sensation and allowing the cosmetic to be applied in a refreshing manner.
しかも、化粧料塗布表面が微細な凹凸構造であり、且つ
通気性、透水性を有するため、水が蒸発し易く、水の蒸
発により化粧料塗布表面が冷却され、従って、塗布時に
より一層清涼感を得られる。Moreover, since the cosmetic application surface has a fine uneven structure and has air permeability and water permeability, water evaporates easily, and the evaporation of water cools the cosmetic application surface, resulting in an even more refreshing feeling during application. You can get
また、本発明の化粧用塗布具素材によれば、発泡体全体
にわたって小孔および微細孔が存在するので、化粧用塗
布具を水に濡らした際の保水量が増加する。Further, according to the cosmetic applicator material of the present invention, since small pores and micropores are present throughout the foam, the amount of water retained when the cosmetic applicator is wetted with water is increased.
更に、発泡体に繊維粉末を混入した場合は、感触が良好
となる。しかも、IIN粉末を親水性のものとすると、
より一層優れた吸水性および水に濡れた場合の冷却効果
を得ることができる。Furthermore, when fiber powder is mixed into the foam, the feel becomes better. Moreover, if the IIN powder is made hydrophilic,
Even better water absorbency and cooling effect when wet can be obtained.
本発明の化粧用塗布具素材はソフトな感触であるので、
水性メイクアップ化粧料用塗布具としてだけでなく、他
の化粧料、例えば液状化粧料、の塗布具としても適して
いる。Since the cosmetic applicator material of the present invention has a soft feel,
It is suitable not only as an applicator for aqueous makeup cosmetics, but also as an applicator for other cosmetics, such as liquid cosmetics.
Claims (1)
クスを主成分とした発泡体であり、該発泡体は気泡によ
り形成された小孔の他に、水または水溶液に溶解可能な
微粒子の溶出により形成された微細孔を有していること
を特徴とする化粧用塗布具素材。 2、通気性を有し且つ乾燥状態でも柔軟なゴムラテック
スを主成分とした発泡体であり、該発泡体は気泡により
形成された小孔の他に、水または水溶液に溶解可能な微
粒子の溶出により形成された微細孔を有しており、更に
繊維粉末を含んでいることを特徴とする化粧用塗布具素
材。 3、水または水溶液に溶解可能な微粒子をゴムラテック
スを主成分とする液中に混入配合し、該混合液に気体を
吹込むかまたは発泡剤を混合し、泡立ち状態で凝固させ
、加硫して、ゴムラテックス発泡体を形成し、該ゴムラ
テックス発泡体を水または水溶液で洗浄して、ゴムラテ
ックス発泡体から前記微粒子を溶出させて微細孔を形成
することを特徴とする化粧用塗布具素材の製造方法。 4、繊維粉末と、水または水溶液に溶解可能な微粒子と
をゴムラテックスを主成分とする液中に混入配合し、該
混合液に気体を吹込むかまたは発泡剤を混合して、泡立
ち状態で凝固させ、加硫して、ゴムラテックス発泡体を
形成し、該ゴムラテックス発泡体を水または水溶液で洗
浄して、ゴムラテックス発泡体から前記微粒子を溶出さ
せて微細孔を形成することを特徴とする化粧用塗布具素
材の製造方法。[Claims] 1. A foam mainly composed of rubber latex that is breathable and flexible even in a dry state, and the foam has small pores formed by air bubbles as well as water or an aqueous solution. A cosmetic applicator material characterized by having micropores formed by the elution of fine particles that can be dissolved in. 2. It is a foam mainly composed of rubber latex, which is breathable and flexible even in a dry state, and in addition to small pores formed by air bubbles, the foam also has the ability to elute microparticles that can be dissolved in water or an aqueous solution. A cosmetic applicator material characterized by having micropores formed by the above method and further containing fiber powder. 3. Mix and blend fine particles that can be dissolved in water or an aqueous solution into a liquid mainly composed of rubber latex, blow gas into the mixed liquid or mix a foaming agent, solidify in a foamy state, and vulcanize. A cosmetic applicator material characterized in that a rubber latex foam is formed, and the rubber latex foam is washed with water or an aqueous solution to elute the fine particles from the rubber latex foam and form micropores. manufacturing method. 4. Fiber powder and fine particles that can be dissolved in water or an aqueous solution are mixed and blended into a liquid mainly composed of rubber latex, and a gas is blown into the mixed liquid or a foaming agent is mixed to form a foaming state. The rubber latex foam is coagulated and vulcanized to form a rubber latex foam, and the rubber latex foam is washed with water or an aqueous solution to elute the fine particles from the rubber latex foam and form micropores. A method for manufacturing a cosmetic applicator material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8040087A JPS63246103A (en) | 1987-03-31 | 1987-03-31 | Material for cosmetics application and its production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8040087A JPS63246103A (en) | 1987-03-31 | 1987-03-31 | Material for cosmetics application and its production |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63246103A true JPS63246103A (en) | 1988-10-13 |
JPH0455042B2 JPH0455042B2 (en) | 1992-09-02 |
Family
ID=13717237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8040087A Granted JPS63246103A (en) | 1987-03-31 | 1987-03-31 | Material for cosmetics application and its production |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63246103A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0444812U (en) * | 1990-08-10 | 1992-04-16 | ||
KR200466010Y1 (en) * | 2011-12-14 | 2013-03-25 | (주)아모레퍼시픽 | Cooling powder Puff |
-
1987
- 1987-03-31 JP JP8040087A patent/JPS63246103A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0444812U (en) * | 1990-08-10 | 1992-04-16 | ||
KR200466010Y1 (en) * | 2011-12-14 | 2013-03-25 | (주)아모레퍼시픽 | Cooling powder Puff |
Also Published As
Publication number | Publication date |
---|---|
JPH0455042B2 (en) | 1992-09-02 |
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