JP7104392B1 - 人工爪組成物 - Google Patents
人工爪組成物 Download PDFInfo
- Publication number
- JP7104392B1 JP7104392B1 JP2022098976A JP2022098976A JP7104392B1 JP 7104392 B1 JP7104392 B1 JP 7104392B1 JP 2022098976 A JP2022098976 A JP 2022098976A JP 2022098976 A JP2022098976 A JP 2022098976A JP 7104392 B1 JP7104392 B1 JP 7104392B1
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- JP
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- Prior art keywords
- artificial nail
- meth
- nail
- component
- nail composition
- 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.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 94
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- 238000010586 diagram Methods 0.000 abstract 1
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- 238000011156 evaluation Methods 0.000 description 17
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
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- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 2
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- LWMFAFLIWMPZSX-UHFFFAOYSA-N bis[2-(4,5-dihydro-1h-imidazol-2-yl)propan-2-yl]diazene Chemical compound N=1CCNC=1C(C)(C)N=NC(C)(C)C1=NCCN1 LWMFAFLIWMPZSX-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
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- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 2
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- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
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- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
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Abstract
Description
(A)成分:分子内に少なくとも1個のラジカル重合性不飽和二重結合を有する化合物
(B)成分:以下の式で表される化合物
本実施形態に係る人工爪組成物は、(A)成分:分子内に少なくとも1個のラジカル重合性不飽和二重結合を有する化合物と、(B)成分:分子内に少なくとも1個のラジカル重合性不飽和二重結合を有する酸性リン化合物と、(C)成分:ラジカル重合開始剤とを含有する。
(A)成分の種類は、特に限定されない。例えば、単官能モノマーとして、メチル(メタ)アクリレート、エチル(メタ)アクリレート、プロピル(メタ)アクリレート、ブチル(メタ)アクリレート、アミル(メタ)アクリレート、ヘキシル(メタ)アクリレート、ヘプチル(メタ)アクリレート等のアルキル(メタ)アクリレート、アルキルフェノールのアルキレンオキサイド付加物の(メタ)アクリレート、シクロヘキシル(メタ)アクリレート、及びベンジル(メタ)アクリレート等が挙げられる。
本実施形態において、(B)成分は、以下の式で表される化合物である。
n=2の場合:ビス(メタクリロキシイソプロピル)-フォスフェート
本実施形態に記載の人工爪組成物は、ラジカル重合開始剤を含有する。カチオン重合開始剤の使用は、毒性の問題を生じ得るため好ましくない。
人工爪組成物が光硬化性である場合、(C)成分は、光の作用によりラジカル共重合を開始させる能力を有するものであれば特に限定されない。例えば、4-フェノキシジクロロアセトフェノン、4-t-ブチル-ジクロロアセトフェノン、4-t-ブチル-トリクロロアセトフェノン、ジエトキシアセトフェノン、2-ヒドロキシ-2-フェニル-1-フェニルプロパン-1-オン、1-(4-ドデシルフェニル)-2-ヒドロキシ-2-メチルプロパン-1-オン、1-(4-イソプロピルフェニル)-2-ヒドロキシ-2-メチルプロパン-1-オン、4-(2-ヒドロキシエトキシ)-フェニル-(2-ヒドロキシ-2-プロピル)ケトン、1-ヒドロキシシクロヘキシルフェニルケトン、2-メチル-1-[4-(メチルチオ)フェニル]-2-モルホリノプロパン-1等のアセトフェノン系開始剤;ベンゾイン、ベンゾインメチルエーテル、ベンゾインイソプロピルエーテル、ベンゾインイソブチルエーテル、ベンジルメチルケタール等のベンゾイン系開始剤;ベンゾフェノン、ベンゾイル安息香酸、ベンゾイル安息香酸メチル、4-フェニルベンゾフェノン、ヒドロキシベンゾフェノン、アクリル化ベンゾフェノン、4-ベンゾイル-4’-メチルジフェニルサルファイド、3,3’-ジメチル-4-メトキシベンゾフェノン、4,4’-ジメチルアミノベンゾフェノン、4,4’-ジエチルアミノベンゾフェノン、3,3’,4,4’-テトラ(t-ブチルパーオキシカルボニル)ベンゾフェノン等のベンゾフェノン系開始剤;チオキサントン、2-クロロチオキサントン、2-メチルチオキサントン、2,4-ジメチルチオキサントン、2,4-ジエチルチオキサントン、2,4-ジイソプロピルチオキサントン、イソプロピルチオキサントン、1-クロロ-4-プロポキシチオキサントン、2,4-ジクロロチオキサントン等のチオキサントン系開始剤;α-アシロキシムエステル、メチルフェニルグリオキシレート、ベンジル、9,10-フェナンスレンキノン、カンファーキノン、ジベンゾスベロン、2-エチルアントラキノン、4’,4’’-ジエチルイソフタロフェノン等のケトン系開始剤;2,2’-ビス(2-クロロフェニル)-4,4’,5,5’-テトラフェニル-1,2’-イミダゾール等のイミダゾール系開始剤;2,4,6-トリメチルベンゾイルジフェニルホスフィンオキサイド等のアシルホスフィンオキサイド系開始剤;カルバゾール系開始剤等が挙げられる。
人工爪組成物が熱硬化性である場合、(C)成分は、常温熱硬化性を有することが好ましい。
本実施形態の人工爪組成物には、必要に応じて、公知の各種添加剤を配合することができる。かかる添加剤の例としては、重合促進剤、重合禁止剤、着色剤、変色防止剤、蛍光剤、紫外線吸収剤、抗菌剤、揮発性有機溶媒等が挙げられる。
はない。
〔使用した成分〕
(A)1分子中に1個以上のラジカル重合性不飽和結合を有するラジカル重合性化合物
A1:ウレタンアクリレートオリゴマー(ポリエーテル系、重量平均分子量:15000)
A2:ウレタンアクリレートオリゴマー(ポリエーテル系、重量平均分子量:4500)
A3:2-ヒドロキシプロピルメタクリレート
A4:イソボルニルメタクリレート
B1:メタクリロキシイソプロピルフォスフェート(実施例)
B2:ビス(メタクリロキシイソプロピル)フォスフェート(実施例)
B3:2-メタクリロキシエチルフォスフェート(比較例)
B4:ビス(2-メタクリロキシエチル)-フォスフェート(比較例)
B5:エチルアシッドホスフェート(比較例)
n=2の場合:ビス(2-メタクリロキシエチル)-フォスフェート(化合物B4)
C1:2,4,6-トリメチルベンゾイルジフェニルホスフィンオキサイド
表1-5の調整混合に従い、上記A1-A4、B1-B5、C1の成分を電子天秤により計量後、攪拌混合して実施例1-8、比較例1-14に係る人工爪組成物を調製した。
調製した人工爪組成物それぞれについて、以下に示す手順で接着性試験1及び2並びに除去性試験1及び2を行った。
[接着性試験1]
接着性試験1では、人工爪組成物を平滑ガラス面(スライドガラス)に塗布し、硬化させた場合の接着性(接着性1)を評価した。接着性試験1の詳細な手順を以下に示す。
まず、スライドガラス(松浪硝子工業社製S1214)を無水エタノールで洗浄し、これを被着体とする。
続いて、スライドガラス上の人工爪組成物硬化体の長手方向より、カミソリ刃(フェザー社製、剃刀替刃(片刃))をガラス板に対して25°の角度で侵入させ、人工爪組成物硬化体がスライドガラス上から剥離するように押し込む。
接着性試験2では、人工爪組成物を被験者の天然爪に塗布して硬化後、一定期間の日常生活を送った後の人工爪組成物の接着性(接着性2)を評価した。接着性試験2の詳細な手順を以下に示す。
ジェルネイル用ネイルファイル(爪やすり、粗さ:600グリッド)を使用して、天然爪表面を削り新鮮面を得る。
美粧を天然爪上に施した状態で、被験者は、14日間の日常生活を送る。そして、14日間の日常生活を送った後の天然爪上の人工爪組成物硬化体の状態を表7の尺度で分類したものを接着性試験2の評価点(接着性2)とする。
除去性試験1では、スライドガラス上で硬化させた人工爪組成物の接着状態、膨潤状態、及びプラスチックバチュラ侵入時の強度を用いて、人工爪組成物の除去性(除去性1)を評価した。除去性試験1の詳細な手順を以下に示す。
除去性試験1用サンプルの作製手順は、接着性試験1と同様である。
作製した除去性試験1用サンプルを浸漬液(アセトン)に10分間浸漬する。そして、浸漬した除去性評価用サンプルを浸漬液から取り出し、浸漬液をふき取る。
除去性試験2では、接着性試験2と同様に人工爪組成物を被験者の天然爪に塗布して硬化後、一定期間の日常生活を送った後の人工爪組成物の除去性(除去性2)を評価した。除去性試験2の詳細な手順を以下に示す。
除去性試験2用サンプルの作製は、接着性試験2と同様である。
除去性試験2用サンプルの作製による美粧を天然爪上に施した状態で、被験者は、14日間の日常生活を送る。
接着性試験1及び2並びに除去性試験1及び2の結果を表10に示す。
表10に示した試験結果について、考察する。
接着性1が「××」「×」の人工爪組成物は、爪甲表面に対する良好な接着性がなく短期間で剥離及び/又は脱落を生じると推測される。一方、接着性1が「〇」の人工爪組成物は、爪甲表面に対する良好な接着性があり、爪甲表面に対して長期に渡り接着し、剥離及び脱落が生じないと推測される。
除去性1が「××」「×」の人工爪組成物は、その硬化物を爪甲表面から容易に除去することが困難であり、無理に除去することにより爪甲表面にダメージを与える可能性があると推測される。一方、除去性1が「〇〇」「〇」「◎◎」「◎」の人工爪組成物は、爪甲表面からの硬化物の除去性が良好であり、爪甲表面にダメージを与えることなく除去可能であると推測される。
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JP2010053097A (ja) | 2008-08-29 | 2010-03-11 | Shofu Inc | 接着性の改善された人工爪組成物 |
WO2014041692A1 (ja) | 2012-09-14 | 2014-03-20 | 東洋アルミニウム株式会社 | 着色金属顔料およびその製造方法 |
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JP2021161057A (ja) | 2020-03-31 | 2021-10-11 | 三菱ケミカル株式会社 | 水溶性抗フケ剤内包ポリマー粒子、化粧料用組成物及び毛髪洗浄料 |
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