JPH0580958B2 - - Google Patents
Info
- Publication number
- JPH0580958B2 JPH0580958B2 JP26917786A JP26917786A JPH0580958B2 JP H0580958 B2 JPH0580958 B2 JP H0580958B2 JP 26917786 A JP26917786 A JP 26917786A JP 26917786 A JP26917786 A JP 26917786A JP H0580958 B2 JPH0580958 B2 JP H0580958B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- composition
- formula
- copolymer
- independently
- 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 - Lifetime
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 28
- 239000002904 solvent Substances 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 5
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 5
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000004859 Copal Substances 0.000 claims description 4
- 241000782205 Guibourtia conjugata Species 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229920001800 Shellac Polymers 0.000 claims description 4
- 125000005907 alkyl ester group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000004208 shellac Substances 0.000 claims description 4
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 claims description 4
- 229940113147 shellac Drugs 0.000 claims description 4
- 235000013874 shellac Nutrition 0.000 claims description 4
- 229920002871 Dammar gum Polymers 0.000 claims description 3
- 239000004860 Dammar gum Substances 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 210000000282 nail Anatomy 0.000 description 35
- 229920001577 copolymer Polymers 0.000 description 19
- 239000000853 adhesive Substances 0.000 description 13
- 230000001070 adhesive effect Effects 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
- 239000004830 Super Glue Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- -1 alkyl methacrylates Chemical class 0.000 description 5
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 210000004905 finger nail Anatomy 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 2
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- PFHOSZAOXCYAGJ-UHFFFAOYSA-N 2-[(2-cyano-4-methoxy-4-methylpentan-2-yl)diazenyl]-4-methoxy-2,4-dimethylpentanenitrile Chemical compound COC(C)(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)(C)OC PFHOSZAOXCYAGJ-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- URDOJQUSEUXVRP-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C(C)=C URDOJQUSEUXVRP-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229920001651 Cyanoacrylate Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- FHKPLLOSJHHKNU-INIZCTEOSA-N [(3S)-3-[8-(1-ethyl-5-methylpyrazol-4-yl)-9-methylpurin-6-yl]oxypyrrolidin-1-yl]-(oxan-4-yl)methanone Chemical compound C(C)N1N=CC(=C1C)C=1N(C2=NC=NC(=C2N=1)O[C@@H]1CN(CC1)C(=O)C1CCOCC1)C FHKPLLOSJHHKNU-INIZCTEOSA-N 0.000 description 1
- RMKZLFMHXZAGTM-UHFFFAOYSA-N [dimethoxy(propyl)silyl]oxymethyl prop-2-enoate Chemical compound CCC[Si](OC)(OC)OCOC(=O)C=C RMKZLFMHXZAGTM-UHFFFAOYSA-N 0.000 description 1
- PQLVXDKIJBQVDF-UHFFFAOYSA-N acetic acid;hydrate Chemical compound O.CC(O)=O PQLVXDKIJBQVDF-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- ZQMHJBXHRFJKOT-UHFFFAOYSA-N methyl 2-[(1-methoxy-2-methyl-1-oxopropan-2-yl)diazenyl]-2-methylpropanoate Chemical compound COC(=O)C(C)(C)N=NC(C)(C)C(=O)OC ZQMHJBXHRFJKOT-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical class OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- PFBLRDXPNUJYJM-UHFFFAOYSA-N tert-butyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(C)(C)C PFBLRDXPNUJYJM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Description
産業上の利用分野
本発明は、主として手指の爪の美化、装飾に用
いられる人工爪の接着用の接着補助剤組成物に関
する。
従来の技術
近年、特に女性の手指の爪の美化、装飾のため
爪を伸長し、美しい形状に整えることがよく行な
われるようになり、そのために、自分の生爪を伸
長するばかりでなく、所望の形状に成形した合成
樹脂製の人工爪が使用されるようになつている。
このような人工爪は接着剤で生爪に接着して使用
され、その接着には速やかに強力な接着強度を得
る必要から、一般に、シアノアクリレート系のよ
うな、いわゆる瞬間接着剤が用いられる。
発明が解決しようとする問題点
しかし、人工爪は一度接着すると、剥離するこ
とが困難になることがしばしばあり、人工爪を交
換したり、取りはずしのうえで問題がある。そこ
で、強い接着強度と共に、剥離性の良好な接着が
要求されている。
このような事情にかんがみ、本発明者らは強い
接着強度が得られ、かつ、剥離性の良好な人工爪
の接着について種々検討した。その結果、ある種
の高分子物質の溶媒溶液を接着補助剤として用い
ることによりその目的が達成できることを見出
し、本発明を完成するにいたつた。
問題点を解決するための手段
本発明は、低級アルコール、低級アルコールを
80容量%以上含有する含水低級アルコールおよび
酢酸の低級アルキルエステルからなる群から選ば
れる溶媒、および該溶媒に分散または溶解した、
組成物全重量に基づいて、3〜70重量%のロジ
ン、コパル、ダンマルガム、セラツク、式:
INDUSTRIAL APPLICATION FIELD The present invention relates to an adhesion aid composition for adhering artificial nails, which is mainly used for beautifying and decorating fingernails. BACKGROUND TECHNOLOGY In recent years, it has become common for women, in particular, to lengthen their fingernails and shape them into beautiful shapes for beautification and decoration. Artificial nails made of synthetic resin molded into shapes have come into use.
Such artificial nails are used by adhering to natural nails with an adhesive, and because it is necessary to quickly obtain strong adhesive strength, so-called instant adhesives such as cyanoacrylate-based adhesives are generally used. Problems to be Solved by the Invention However, once the artificial nails are adhered, it is often difficult to peel them off, which poses problems when replacing or removing the artificial nails. Therefore, in addition to strong adhesive strength, adhesion with good releasability is required. In view of these circumstances, the present inventors have conducted various studies on bonding artificial nails that have strong adhesive strength and good releasability. As a result, the inventors discovered that the objective could be achieved by using a solvent solution of a certain kind of polymeric substance as an adhesion auxiliary agent, and were able to complete the present invention. Means for Solving the Problems The present invention uses lower alcohols and lower alcohols.
A solvent selected from the group consisting of hydrous lower alcohols and lower alkyl esters of acetic acid containing 80% by volume or more, and dispersed or dissolved in the solvent,
Based on the total weight of the composition, 3-70% by weight of rosin, copal, damalgam, shellac, formula:
【化】
[式中、R1およびR2は、各々独立して炭素数1
〜10のアルキル基、R3、R4およびR5は、各々独
立して水素またはメチル基、T、UおよびVは、
各々独立して、0または整数、ただし、10≦T+
U+V≦5000である]
で示される共重合体および式:[In the formula, R 1 and R 2 each independently have a carbon number of 1
~10 alkyl groups, R 3 , R 4 and R 5 are each independently hydrogen or a methyl group, T, U and V are
Each independently, 0 or an integer, provided that 10≦T+
U+V≦5000] Copolymer and formula represented by:
【化】
[式中、R6は炭素数1〜10のアルキル基、R7は
低級アルキル基、R8、R9、R10、R11およびR12
は、各々独立して水素またはメチル基、W、X、
YおよびZは、各々独立して、0または整数、た
だし、10≦W+X+Y+Z≦5000である]で示さ
れる共重合体からなる群から選ばれる高分子物質
からなることを特徴とする人工爪用接着補助剤組
成物を提供するものである。本発明の接着補助剤
組成物は、人工爪の使用に際し、まず、生爪に塗
布される。ついで、常法により、シアノアクリレ
ート系接着剤のような接着剤を用いて人工爪を接
着することにより、速やかに強力な接着強度が得
られる。また、人工爪の接着部周囲にエタノール
を滴下し、少し応力をかけるだけで、所望に応じ
て人工爪を簡単に剥離することができる。
本発明の組成物で溶媒として用いる低級アルコ
ールは炭素数1〜5のものでよく、例えば、メチ
ノール、エタノール、プロパノール、イソプロパ
ノール等が挙げられる。これらの低級アルコール
は含水していてもよいが、高分子物質の分散また
は溶解の観点から、含水低級アルコール中の低級
アルコール濃度は80容量%以上であることが望ま
しい。また、酢酸の低級アルキルエステルとして
は、炭素数1〜5のアルキルエステル、代表的に
は酢酸エチルが挙げられる。本発明においては、
溶媒は、単独でも、あるいは、適宜の割合で2種
以上を混合して用いてもよい。
高分子物質として用いるロジン、コパル、ダン
マルガムおよびセラツクは、いずれも公知の天然
高分子物質であり、通常入手しうるものを使用す
ることができる。
式[]および[]で示される共重合体は、
所定のアクリル系モノマーを特定の比率で、例え
ば、公知の溶液重合法に従つて共重合させること
により得られる。
式[]の共重合体に用いられるモノマーとし
ては、アクリル酸およびメタクリル酸;アクリル
酸メチル、メタクリル酸メチル、アクリル酸エチ
ル、メタクリル酸エチル、メタクリル酸ブチル、
アクリル酸−2−エチルヘキシル、メタクリル酸
−2−エチルヘキシルなどのごときアクリル酸ア
ルキルエステルおよびメタクリル酸アルキルエス
テルが挙げられる。式[]の共重合体中のモノ
マーの重量組成比は、アクリル酸またはメタクリ
ル酸5〜80重量%、好ましくは、25〜50重量%、
1種もしくは2種のアクリル酸エステルまたはメ
タクリル酸エステル20〜95重量%、好ましくは、
50〜75重量%とすることが望ましい。
式[]の共重合体に用いられるモノマーとし
ては、式[]の共重合と同様なモノマーおよ
び、アクリル酸ヒドロキシエチル、メタクリル酸
ヒドロキシエチル、アクリル酸ヒドロキシプロピ
ル、メタクリル酸ヒドロキシプロピルなどのアク
リル酸ヒドロキシアルキルおよびメタクリル酸ヒ
ドロキシアルキル;アクリロキシプロピルトリメ
トキシシラン、メタクリロキシプロピルトリメト
キシシラン、メタクリロキシプロピルトリエトキ
シシランなどのアクリロキシプロピルトリアルコ
キシシランおよびメタクリロキシプロピルトリア
ルコキシシランが挙げられる。式[]の共重合
体中のモノマーの重量組成比は、アクリル酸また
はメタクリル酸5〜30重量%、好ましくは、10〜
20重量%、アクリル酸エステルまたはメタクリル
酸エステル20〜60重量%、好ましくは、25〜40重
量%、アクリル酸ヒドロキシアルキルまたはメタ
クリル酸ヒドロキシアルキル20〜60重量%、好ま
しくは、30〜50重量%、アクリロキシプロピルト
リアルコキシシランまたはメタクリロキシプロピ
ルトリアルコキシシラン0.2〜20重量%、好まし
くは、1〜10重量%とすることが望ましい。
式[]および[]の共重合体の重量平均分
子量は数千〜数十万とすることが好ましい。溶液
重合の際に用いる溶媒としては、メタノール、エ
タノール、イソプロパノール、アセトン、クロロ
ホルム、酢酸エチルなどが挙げられる。また、公
知のラジカル形成性の重合触媒、例えば、2,
2′−アゾビスイソブチロニトリル、2,2′−アゾ
ビス(4−メトキシ−2,4−ジメチルバレロニ
トリル)、ジメチル2,2′−アゾビスイソブチレ
ート、2,2′−アゾビス(2,4−ジメチルバレ
ロニトリル)、ベンゾイルパーオキシド、ジイソ
プロピルパージカーボネート、t−ブチルパーイ
ソブチレートなどを用いることができ、モノマー
全重量に対して0.05〜2重量%の割合で用いるこ
とが好ましい。重合反応は、一般に、溶媒の沸点
以下の50〜100℃で行なうことが好ましい。得ら
れた共重合体溶液は、精製することなく、そのま
ま使用してもよく、また、共重合体を単離、精製
してもよい。
本発明の組成物においては、前記の天然高分子
物質および式[]および[]の共重合体から
選ばれる1種または2種以上の高分子物質を用い
る。該高分子物質は組成物全体に基づいて、3〜
70重量%、好ましくは、10〜30重量%配合する。
3重量%より少ないと、生爪に塗布しても充分な
厚さの被膜が形成できず、人工爪脱着時の剥離性
が悪くなる。一方、70重量%より多くなると、組
成物が粘稠になりすぎ、塗布しにくくなる。
本発明の組成物は、常法に従つて、高分子物質
を溶媒中に溶解または分散することにより製造で
き、所望により、有機または無機の着色剤、香料
のような添加剤を適宜配合してもよい。
本発明の組成物を使用するには、人工爪の装着
に際し、まず、適宜の方法で生爪に塗布し、風乾
する。ついで、シアノアクリレート系接着剤等で
常法に従つて人工爪を接着する。接着した人工爪
は冷水、温水、洗剤液等に浸漬しても剥離するこ
とはない。脱着時には、人工爪の接着部周囲にエ
タノールを滴下し、わずかに応力をかけるだけで
人工爪を生爪から容易に剥離できる。
発明の効果
本発明の組成物を用いることにより、人工爪の
装着に際して要求される強い接着強度の達成と共
に、良好な剥離性が達成できる。
実施例
つぎに参考例、実施例および比較例を挙げて本
発明をさらに詳しく説明する。
参考例 1
温度計、還流管、窒素導入管を設置した三口フ
ラスコ中にメタクリル酸15g、メタクリル酸メチ
ル20g、メタクリル酸ブチル15gからなる30%エ
タノール溶液を調製し、窒素気流下にて1〜2時
間攪拌して脱気した。つぎに2,2′−アゾビス
(2,4−ジメチルバレロニトリル)0.25gを加
え、60℃で20時間重合させた後、更に重合開始触
媒0.2gを追添加し、78℃で4時間重合を行ない、
反応を完結させた。エタノールで希釈して無色透
明な20%共重合体(式[]、T:U:V=3:
4:3、R1、R3、R4、R5=メチル、R2=ブチ
ル、分子量75000)溶液を得た。
参考例 2
温度計、還流管、窒素導入管を設置した三口フ
ラスコ中にメタクリル酸5g、メタクリル酸メチ
ル5g、メタクリル酸ヒドロキシエチル10g、メ
タクリロキシプロピルトリメトキシシラン5gか
らなる30%エタノール溶液を調製し、窒素気流下
にて1〜2時間攪拌して脱気した。つぎに2,
2′−アゾビス(2,4−ジメチルバレロニトリ
ル)0.25gを加え、60℃で20時間重合させた後、
更に重合触媒0.2gを追添加し、78℃で4時間重
合を行ない、反応を完結させた。エタノールで希
釈して無色透明な20%共重合体(式[]、W:
X:Y:Z=1:1:2:1、R6〜R12=メチ
ル、分子量50000)溶液を得た。
実施例 1
参考例1で得られた式[]の共重合体3.0g
を無水エタノールに溶解し、全量を10gとして所
望の人工爪用接着補助剤組成物を得る。
実施例 2
参考例2で得られた式[]の共重合体2.0g
を無水エタノールに溶解し、全量を10gとして所
望の組成物を得る。
実施例 3
参考例2で得られた式[]の共重合体2.0g
およびロジン2.0gを80%エタノールに溶解し、
全量を10gとして所望の組成物を得る。
実施例 4
コパル樹脂0.5gを無水メタノールに溶解し、
全量を10gとして所望の組成物を得る。
実施例 5
ロジン2.0gを酢酸エチルに溶解し、全量を10
gとして所望の組成物を得る。
実施例 6
ダルマルガム2.0gを90%エタノールに溶解し、
全量を10gとして所望の組成物を得る。
実施例 7
セラツク2.0gを無水エタノールに溶解し、全
量を10gとして所望の組成物を得る。
実施例 8
参考例1で得られた式[]の共重合体1.0g
およびダンマルガム1.5gをイソプロパノールに
溶解し、全量を10gとして所望の組成物を得る。
比較例 1
参考例2で得られた式[]の共重合体0.2g
を無水エタノールに溶解し、全量を10gとする。
比較例 2
参考例2で得られた式[]の共重合体8gを
無水エタノールに溶解し、全量を10gとする。
これらの実施例および比較例で得られた組成物
を、各々、被験者の手指の爪に小筆で塗布し、風
乾した後、シアノアクリレート系接着剤を用い、
メタクリル酸メチル樹脂製の人工爪を接着した。
ついで、被験者に通常の生活を3時間させ、その
間の人工爪の剥離の有無を調べた。また、3時間
で剥離しない場合、人工爪接着部位にエタノール
を塗布し、応力をかけて剥離し、剥離のしやすさ
をつぎの基準を評価した。組成物の塗布しやす
さ、総合評価も行なつた。
剥離しやすさ
○:容易 ×:困難
塗布しやすさ
○:容易 ×:困難
総合評価
○:良好 ×:不良
結果を第1表に示す。なお、第1表中、比較対
照として、さらに、つぎの接着方法について評価
した結果も示す。
比較例 3
酢酸セルロース−水エマルジヨン系接着剤を予
め生爪に塗布、風乾後、シアノアクリレート系接
着剤で人工爪を接着し、同様に評価した。
比較例 4
シアノアクリレート系接着剤で直接生爪に人工
爪を接着し、同様に評価した。
比較例 5
両面粘着テープのみで人工爪を接着し、同様に
評価した。[Formula, R 6 is an alkyl group having 1 to 10 carbon atoms, R 7 is a lower alkyl group, R 8 , R 9 , R 10 , R 11 and R 12
are each independently hydrogen or methyl group, W, X,
Y and Z are each independently 0 or an integer, provided that 10≦W+X+Y+Z≦5000. An adjuvant composition is provided. When using an artificial nail, the adhesion aid composition of the present invention is first applied to a natural nail. Then, by adhering the artificial nail using an adhesive such as a cyanoacrylate adhesive in a conventional manner, strong adhesive strength can be quickly obtained. Furthermore, by simply dropping ethanol around the adhesive part of the artificial nail and applying a slight stress, the artificial nail can be easily peeled off as desired. The lower alcohol used as a solvent in the composition of the present invention may have 1 to 5 carbon atoms, and includes, for example, methynol, ethanol, propanol, isopropanol, and the like. These lower alcohols may contain water, but from the viewpoint of dispersing or dissolving the polymeric substance, it is desirable that the lower alcohol concentration in the water-containing lower alcohol is 80% by volume or more. Examples of lower alkyl esters of acetic acid include alkyl esters having 1 to 5 carbon atoms, typically ethyl acetate. In the present invention,
The solvents may be used alone or in combination of two or more in an appropriate ratio. Rosin, copal, dammargum and shellac used as polymeric substances are all known natural polymeric substances, and commonly available ones can be used. The copolymers represented by the formulas [] and [] are
It can be obtained by copolymerizing predetermined acrylic monomers in a specific ratio, for example, according to a known solution polymerization method. Monomers used in the copolymer of formula [] include acrylic acid and methacrylic acid; methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl methacrylate,
Examples include alkyl acrylates and alkyl methacrylates such as 2-ethylhexyl acrylate and 2-ethylhexyl methacrylate. The weight composition ratio of the monomers in the copolymer of formula [] is 5 to 80% by weight of acrylic acid or methacrylic acid, preferably 25 to 50% by weight,
20-95% by weight of one or two acrylic esters or methacrylic esters, preferably
The content is preferably 50 to 75% by weight. Monomers used in the copolymer of formula [] include the same monomers as those for the copolymer of formula [], and hydroxy acrylates such as hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, and hydroxypropyl methacrylate. Alkyl and hydroxyalkyl methacrylates; include acryloxypropyltrialkoxysilanes and methacryloxypropyltrialkoxysilanes such as acryloxypropyltrimethoxysilane, methacryloxypropyltrimethoxysilane, methacryloxypropyltriethoxysilane. The weight composition ratio of the monomers in the copolymer of formula [] is 5 to 30% by weight of acrylic acid or methacrylic acid, preferably 10 to 30% by weight.
20% by weight, 20-60% by weight of acrylic ester or methacrylic ester, preferably 25-40% by weight, 20-60% by weight of hydroxyalkyl acrylate or hydroxyalkyl methacrylate, preferably 30-50% by weight, It is desirable that the amount of acryloxypropyltrialkoxysilane or methacryloxypropyltrialkoxysilane be 0.2 to 20% by weight, preferably 1 to 10% by weight. The weight average molecular weight of the copolymers of formulas [] and [] is preferably from several thousand to several hundred thousand. Examples of the solvent used during solution polymerization include methanol, ethanol, isopropanol, acetone, chloroform, and ethyl acetate. In addition, known radical-forming polymerization catalysts such as 2,
2'-azobisisobutyronitrile, 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile), dimethyl 2,2'-azobisisobutyrate, 2,2'-azobis(2 , 4-dimethylvaleronitrile), benzoyl peroxide, diisopropyl perdicarbonate, t-butyl perisobutyrate, etc., and are preferably used in a proportion of 0.05 to 2% by weight based on the total weight of the monomers. The polymerization reaction is generally preferably carried out at a temperature of 50 to 100°C below the boiling point of the solvent. The obtained copolymer solution may be used as it is without being purified, or the copolymer may be isolated and purified. In the composition of the present invention, one or more polymeric substances selected from the above-mentioned natural polymeric substances and copolymers of formulas [] and [] are used. Based on the entire composition, the polymeric material has a content of 3 to 3.
70% by weight, preferably 10 to 30% by weight.
If it is less than 3% by weight, a film of sufficient thickness cannot be formed even when applied to natural nails, and removability when attaching and removing artificial nails becomes poor. On the other hand, if it exceeds 70% by weight, the composition becomes too viscous and difficult to apply. The composition of the present invention can be produced by dissolving or dispersing a polymer substance in a solvent according to a conventional method, and if desired, additives such as organic or inorganic colorants and fragrances may be appropriately added. Good too. To use the composition of the present invention, when attaching an artificial nail, it is first applied to a natural nail by an appropriate method and air-dried. Then, the artificial nail is adhered using a cyanoacrylate adhesive or the like in a conventional manner. Bonded artificial nails will not peel off even if immersed in cold water, hot water, detergent solution, etc. When attaching and detaching, the artificial nail can be easily separated from the natural nail by dropping ethanol around the adhesive part of the artificial nail and applying a slight stress. Effects of the Invention By using the composition of the present invention, it is possible to achieve the strong adhesive strength required when attaching artificial nails, as well as good releasability. EXAMPLES Next, the present invention will be described in more detail with reference to reference examples, examples, and comparative examples. Reference Example 1 A 30% ethanol solution consisting of 15 g of methacrylic acid, 20 g of methyl methacrylate, and 15 g of butyl methacrylate was prepared in a three-necked flask equipped with a thermometer, a reflux tube, and a nitrogen inlet tube, and the mixture was heated under a nitrogen stream for 1 to 2 hours. It was degassed by stirring for an hour. Next, 0.25 g of 2,2'-azobis(2,4-dimethylvaleronitrile) was added and polymerized at 60°C for 20 hours. Then, 0.2 g of a polymerization initiation catalyst was added and polymerization was continued at 78°C for 4 hours. conduct,
The reaction was completed. A colorless and transparent 20% copolymer (formula [], T:U:V=3:
4:3, R 1 , R 3 , R 4 , R 5 = methyl, R 2 = butyl, molecular weight 75000) solution was obtained. Reference Example 2 A 30% ethanol solution consisting of 5 g of methacrylic acid, 5 g of methyl methacrylate, 10 g of hydroxyethyl methacrylate, and 5 g of methacryloxypropyltrimethoxysilane was prepared in a three-necked flask equipped with a thermometer, reflux tube, and nitrogen inlet tube. The mixture was degassed by stirring for 1 to 2 hours under a nitrogen stream. Next 2,
After adding 0.25 g of 2'-azobis(2,4-dimethylvaleronitrile) and polymerizing at 60°C for 20 hours,
Further, 0.2 g of a polymerization catalyst was added and polymerization was carried out at 78° C. for 4 hours to complete the reaction. A colorless and transparent 20% copolymer (formula [], W:
A solution was obtained (X:Y:Z=1:1:2:1, R6 to R12 = methyl, molecular weight 50000). Example 1 3.0 g of copolymer of formula [] obtained in Reference Example 1
was dissolved in absolute ethanol to give a total amount of 10 g to obtain a desired adhesive composition for artificial nails. Example 2 2.0 g of copolymer of formula [ ] obtained in Reference Example 2
was dissolved in absolute ethanol to give a total amount of 10 g to obtain the desired composition. Example 3 2.0 g of copolymer of formula [] obtained in Reference Example 2
Dissolve 2.0g of rosin in 80% ethanol,
The desired composition is obtained with a total amount of 10 g. Example 4 0.5 g of copal resin was dissolved in anhydrous methanol,
The desired composition is obtained with a total amount of 10 g. Example 5 Dissolve 2.0 g of rosin in ethyl acetate and dilute the total amount to 10
The desired composition is obtained as g. Example 6 2.0g of Dharmal gum was dissolved in 90% ethanol,
The desired composition is obtained with a total amount of 10 g. Example 7 2.0 g of shellac is dissolved in absolute ethanol to give a total amount of 10 g to obtain the desired composition. Example 8 1.0 g of copolymer of formula [] obtained in Reference Example 1
and 1.5 g of dammar gum are dissolved in isopropanol to give a total amount of 10 g to obtain the desired composition. Comparative Example 1 0.2 g of copolymer of formula [] obtained in Reference Example 2
Dissolve in absolute ethanol to make a total amount of 10 g. Comparative Example 2 8 g of the copolymer of formula [] obtained in Reference Example 2 was dissolved in absolute ethanol to make the total amount 10 g. The compositions obtained in these Examples and Comparative Examples were each applied to the test subject's fingernails with a small brush, air-dried, and then applied using a cyanoacrylate adhesive.
Artificial nails made of methyl methacrylate resin were glued on.
Next, the test subjects were allowed to live their normal lives for 3 hours, and the presence or absence of peeling of the artificial nails during that time was examined. In addition, if the artificial nail did not peel off within 3 hours, ethanol was applied to the artificial nail adhesion site and the nail was peeled off by applying stress, and the ease of peeling was evaluated using the following criteria. A comprehensive evaluation of the ease of application of the composition was also conducted. Ease of peeling ○: Easy ×: Difficult Ease of application ○: Easy ×: Difficult Overall evaluation ○: Good ×: Poor The results are shown in Table 1. In addition, Table 1 also shows the results of evaluation of the following adhesion method as a comparison. Comparative Example 3 A cellulose acetate-water emulsion adhesive was applied to natural nails in advance, and after air drying, an artificial nail was adhered with a cyanoacrylate adhesive and evaluated in the same manner. Comparative Example 4 An artificial nail was directly adhered to a natural nail using a cyanoacrylate adhesive and evaluated in the same manner. Comparative Example 5 An artificial nail was adhered using only double-sided adhesive tape and evaluated in the same manner.
【表】【table】
【表】
第1表に示すごとく、本発明の人工爪用接着補
助剤組成物を用いることにより、望ましい人工爪
の接着を行なうことができる。[Table] As shown in Table 1, by using the adhesion aid composition for artificial nails of the present invention, desirable adhesion of artificial nails can be achieved.
Claims (1)
以上含有する含水低級アルコールおよび酢酸の低
級アルキルエステルからなる群から選ばれる溶
媒、および該溶媒に分散または溶解した、組成物
全重量に基づいて、3〜70重量%のロジン、コパ
ル、ダンマルガム、セラツク、式: 【化】 [式中、R1およびR2は、各々独立して炭素数1
〜10のアルキル基、R3、R4およびR5は、各々独
立して水素またはメチル基、T、UおよびVは、
各々独立して、0または整数、ただし、10≦T+
U+V≦5000である] で示される共重合体および式: 【化】 [式中、R6は炭素数1〜10のアルキル基、R7は
低級アルキル基、R8、R9、R10、R11およびR12
は、各々独立して水素またはメチル基、W、X、
YおよびZは、各々独立して、0または整数、た
だし、10≦W+X+Y+Z≦5000である]で示さ
れる共重合体からなる群から選ばれる高分子物質
からなることを特徴とする人工爪用接着補助剤組
成物。[Claims] 1. Lower alcohol, 80% by volume of lower alcohol
A solvent selected from the group consisting of water-containing lower alcohols and lower alkyl esters of acetic acid, and 3 to 70% by weight of rosin, copal, dammargum, and shellac, based on the total weight of the composition, dispersed or dissolved in the solvent. , formula: [In the formula, R 1 and R 2 each independently have a carbon number of 1
~10 alkyl groups, R 3 , R 4 and R 5 are each independently hydrogen or a methyl group, T, U and V are
Each independently, 0 or an integer, provided that 10≦T+
[wherein R 6 is an alkyl group having 1 to 10 carbon atoms, R 7 is a lower alkyl group, R 8 , R 9 , R 10 , R11 and R12
are each independently hydrogen or methyl group, W, X,
Y and Z are each independently 0 or an integer, provided that 10≦W+X+Y+Z≦5000. Adjuvant composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26917786A JPS63122771A (en) | 1986-11-12 | 1986-11-12 | Bonding assistant composition for artificial nail |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26917786A JPS63122771A (en) | 1986-11-12 | 1986-11-12 | Bonding assistant composition for artificial nail |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63122771A JPS63122771A (en) | 1988-05-26 |
JPH0580958B2 true JPH0580958B2 (en) | 1993-11-10 |
Family
ID=17468749
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26917786A Granted JPS63122771A (en) | 1986-11-12 | 1986-11-12 | Bonding assistant composition for artificial nail |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63122771A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2870454B1 (en) * | 2004-05-19 | 2006-08-25 | Oreal | AQUEOUS NAIL POLISH FILM |
FR2870453B1 (en) * | 2004-05-19 | 2006-08-25 | Oreal | NAIL POLISH FILM RETICULE |
WO2007042945A2 (en) * | 2005-10-07 | 2007-04-19 | L'oreal | Process for making up or caring for the nails with cyanoacrylate monomer |
FR2891738B1 (en) * | 2005-10-07 | 2012-08-17 | Oreal | PROCESS FOR MAKE-UP OR CARE OF NAILS WITH CYANOACRYLATE MONOMER |
-
1986
- 1986-11-12 JP JP26917786A patent/JPS63122771A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS63122771A (en) | 1988-05-26 |
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