JPH07126125A - Make-up cosmetic - Google Patents
Make-up cosmeticInfo
- Publication number
- JPH07126125A JPH07126125A JP27813693A JP27813693A JPH07126125A JP H07126125 A JPH07126125 A JP H07126125A JP 27813693 A JP27813693 A JP 27813693A JP 27813693 A JP27813693 A JP 27813693A JP H07126125 A JPH07126125 A JP H07126125A
- Authority
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- Japan
- Prior art keywords
- glass transition
- make
- feeling
- cosmetic
- surface temperature
- Prior art date
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Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、化粧がし易く、使用感
の優れたメイクアップ化粧料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a makeup cosmetic composition which is easy to apply makeup and has an excellent feeling of use.
【0002】[0002]
【従来の技術】ファンデーション、ベースローション等
のメイクアップ化粧料には、耐候性の改善やベト付き感
の解消を目的として、従来から粉体が配合されている。
最近は、化粧料の肌への付着性、化粧持ちなどを改善す
るため、配合する粉体の微粒子化や薄片化が試みられた
り、多孔質粉体が用いられたり、さらには粉体の表面処
理が提案されてきた。表面処理法としては、フッ素系樹
脂で表面処理する方法(特公昭61─48803号公報
参照)、酸化亜鉛、炭酸亜鉛微粒子で表面処理する方法
(特開昭61─257909号公報参照)、二酸化チタ
ン等の金属粉体で被覆する方法(特開昭61─2579
08号公報参照)などが提案されている。2. Description of the Related Art Powders have been conventionally blended in makeup cosmetics such as foundations and base lotions for the purpose of improving weather resistance and eliminating sticky feeling.
Recently, in order to improve the adhesion of cosmetics to the skin and make-up lasting, it has been attempted to make the powder blended into fine particles and flakes, and porous powders have been used. Treatment has been proposed. As the surface treatment method, a method of surface treatment with a fluororesin (see JP-B-61-48803), a method of surface treatment with zinc oxide or zinc carbonate fine particles (see JP-A-61-257909), and titanium dioxide A method of coating with a metal powder such as JP-A-61-2579
No. 08 publication) is proposed.
【0003】[0003]
【発明が解決しようとする課題】ところで、メイクアッ
プ化粧料は、化粧を行うときには皮膚上での滑り感、伸
びの軽さなどが求められ、その後は、人の皮膚との密着
感、通気性、吸水性、給油性等の使用感の良さが求めら
れるが、化粧料に配合する粉体は、化粧時と使用時にお
いて弾性率等の物性がほとんど変化しないため、例えば
化粧時に要求される滑り感を向上させるために、粉体を
固くすると使用時には違和感として感知され、上記の要
望を同時に満たすことは困難であった。By the way, makeup cosmetics are required to have a feeling of slipping on the skin, lightness of elongation and the like when applying makeup, and thereafter, a feeling of close contact with human skin and breathability. , Good absorbability, oil replenishment, etc. are required, but powders mixed in cosmetics have little change in physical properties such as elastic modulus during makeup and during use. When the powder is hardened to improve the feeling, it is perceived as an unpleasant sensation during use, and it is difficult to simultaneously satisfy the above demands.
【0004】そこで、本発明では、化粧時の滑り感、伸
びの軽さ、及び、使用時の密着感、使用感の良さを備え
たメイクアップ化粧料を提供しようとするものである。Therefore, the present invention is intended to provide a makeup cosmetic having a slippery feel at the time of makeup, a light stretch, a close contact feel at the time of use, and a good feel at use.
【0005】[0005]
【課題を解決するための手段】本発明は、ガラス転移点
が皮膚表面温度より低く,皮膚表面温度でガラス転移し
て弾性率が変化する形状記憶樹脂よりなる球状の微細粉
体を配合したことを特徴とするメイクアップ化粧料であ
る。According to the present invention, a spherical fine powder made of a shape memory resin having a glass transition point lower than the skin surface temperature and undergoing a glass transition at the skin surface temperature to change the elastic modulus is blended. Is a makeup cosmetics.
【0006】本発明のメイクアップ化粧料に適した形状
記憶性樹脂は、ガラス転移点前後における弾性率比が4
以上であり、皮膚表面温度近傍における損失正接tan
δが0.3〜0.9の範囲にある形状記憶性樹脂、特に
ポリウレタンを用いることが好ましい。なお、形状記憶
性樹脂は0.01〜80重量%、特に5〜50重量%の
範囲で配合することが好ましい。The shape memory resin suitable for makeup cosmetics of the present invention has an elastic modulus ratio of 4 before and after the glass transition point.
The above is the loss tangent tan near the skin surface temperature
It is preferable to use a shape memory resin having δ in the range of 0.3 to 0.9, particularly polyurethane. The shape memory resin is preferably blended in the range of 0.01 to 80% by weight, particularly 5 to 50% by weight.
【0007】[0007]
【作用】本発明のメイクアップ化粧料中の形状記憶樹脂
よりなる球状の微細粉体は、ガラス転移点より低温のガ
ラス領域にあって高弾性率を有するため、化粧料を皮膚
上に塗布するときに滑りが良くまた伸びに軽さがあり、
化粧を極めて円滑に行うことができる。また、皮膚上に
塗布することにより、上記球状の微細粉体はガラス転移
点より高温の皮膚温度になるため、ゴム領域の低弾性率
を呈し、これが皮膚感触に近く密着感、使用感の向上に
寄与する。The spherical fine powder made of the shape memory resin in the makeup cosmetic of the present invention has a high elastic modulus in the glass region at a temperature lower than the glass transition point, so that the cosmetic is applied onto the skin. Sometimes it slips well and it has a light stretch,
The makeup can be applied very smoothly. In addition, when applied on the skin, the spherical fine powder has a skin temperature higher than the glass transition point, and thus exhibits a low elastic modulus in the rubber region, which is close to the skin feel and improves the adhesion and usability. Contribute to.
【0008】上記微細粉体に形状記憶性を確保するため
には、使用樹脂のガラス転移点を皮膚表面温度より低く
設定することが好ましい。また、上記の使用感を確保す
るためには、ガラス転移点前後における弾性率比を4以
上、特に4〜200に設定することが好ましい。弾性率
比が4より小さいと、化粧時と使用時に適した滑り感や
密着感を充分に確保することができない。In order to ensure the shape memory property of the fine powder, it is preferable to set the glass transition point of the resin used to be lower than the skin surface temperature. Further, in order to secure the above-mentioned feeling of use, it is preferable to set the elastic modulus ratio before and after the glass transition point to 4 or more, particularly 4 to 200. When the elastic modulus ratio is less than 4, it is not possible to sufficiently secure a slippery feeling and a close feeling suitable for makeup and use.
【0009】損失正接tanδは、損失弾性率E”と貯
蔵弾性率E’の比E”/E’と定義される物性であり、
人の皮膚のtanδがおよそ0.5前後である。そこ
で、本発明で化粧料に配合する形状記憶性樹脂微細粉体
の皮膚表面温度近傍における損失正接tanδを0.3
〜0.9、好ましくは0.4〜0.8の範囲に設定する
ことにより、塗布した後の違和感の解消に大きな役割を
する。The loss tangent tan δ is a physical property defined as the ratio E ″ / E ′ of the loss elastic modulus E ″ and the storage elastic modulus E ′,
The tan δ of human skin is about 0.5. Therefore, the loss tangent tan δ in the vicinity of the skin surface temperature of the shape-memory resin fine powder blended in the cosmetic of the present invention is 0.3.
By setting it in the range of 0.9, preferably 0.4 to 0.8, it plays a great role in eliminating discomfort after application.
【0010】上記の形状記憶性、弾性記憶性及び損失正
接tanδの値を備えた樹脂としてはポリウレタンが適
している。本発明で使用するポリウレタンビーズは、懸
濁安定剤を含む水中でポリイソシアネートプレポリマー
単独、又は、ポリイソシアネートプレポリマーにポリウ
レタン若しくはポリウレタンプレポリマーポリオールを
添加し、攪拌速度を調整して目的の粒径の懸濁液を得た
後、加温して反応を開始して、ポリウレタンビーズを生
成し、これを固液分離、洗浄、乾燥して製造することが
できる。ポリウレタンビーズの好ましい平均粒径は5〜
15μmの範囲である。Polyurethane is suitable as the resin having the above-mentioned shape memory property, elastic memory property and loss tangent tan δ. The polyurethane beads used in the present invention are the polyisocyanate prepolymer alone in water containing a suspension stabilizer, or polyurethane or polyurethane prepolymer polyol is added to the polyisocyanate prepolymer, and the stirring speed is adjusted to obtain the target particle size. After obtaining the suspension described above, the reaction can be started by heating to produce polyurethane beads, which can be produced by solid-liquid separation, washing and drying. The preferred average particle size of the polyurethane beads is 5 to
It is in the range of 15 μm.
【0011】[0011]
〔ポリウレタンビーズの製造例1〕窒素ガスで充分に置
換し、乾燥させた2リットルの大きさのオートクレーブ
にポリカプロラクトンジオール813gとイソホロンジ
イソシアネート444gを仕込み、さらに窒素ガスで上
方のガスを置換した後密閉し、120℃で20時間攪拌
混合して反応させた。反応終了後80℃まで冷却してト
ルエン539gを追加して仕込み、均一になるまで攪拌
混合した後、冷却してポリイソシアネートプレポリマー
(I)を得た。このプレポリマーのイソシアネート含有
量は4.62%であり、粘度は230cps(25℃)
であった。[Production Example 1 of polyurethane beads] 813 g of polycaprolactone diol and 444 g of isophorone diisocyanate were charged into a 2 liter autoclave, which had been sufficiently replaced with nitrogen gas and dried, and the upper gas was replaced with nitrogen gas and then sealed. Then, the mixture was reacted with stirring at 120 ° C. for 20 hours. After completion of the reaction, the mixture was cooled to 80 ° C., 539 g of toluene was additionally charged, and the mixture was stirred and mixed until the mixture became uniform, and then cooled to obtain a polyisocyanate prepolymer (I). The isocyanate content of this prepolymer was 4.62% and the viscosity was 230 cps (25 ° C).
Met.
【0012】また、窒素ガスで充分に置換し、乾燥させ
た2リットルの大きさのオートクレーブに3メチル1,
5ペンタジオールとアジピン酸のポリエステルジオール
720gと、イソホロンジイソシアネート54gを仕込
んで反応させ、不揮発分70wt%含有するトルエン溶
液であるポリウレタンポレポリマーポリオール(II)を
得た。このポリオールの水酸基含有量は0.37%であ
り、粘度は570cps(25℃)であった。Further, the autoclave having a size of 2 liters, which had been sufficiently replaced with nitrogen gas and dried, was charged with 3 methyl 1 ,.
520 g of a polyester diol of 5 pentadiol and adipic acid and 54 g of isophorone diisocyanate were charged and reacted to obtain a polyurethane polee polymer polyol (II) as a toluene solution containing a nonvolatile content of 70 wt%. The hydroxyl group content of this polyol was 0.37%, and the viscosity was 570 cps (25 ° C.).
【0013】次に、2リットル攪拌機付きセパラブルフ
ラスコに水980gを仕込み、メチルセルロースを20
0g溶解して分散媒を作成する。この分散媒を600r
pmで攪拌しながら上記ポリイソシアネートプレポリマ
ー(I)200gとポリウレタンポレポリマーポリオー
ル(II)200gとを均一に攪拌混合し、懸濁液を60
℃に昇温して3時間反応させ、その後52℃まで冷却
し、次にセルロース分解酵素7gを添加し、30分間攪
拌した後、100℃に昇温してトルエンを共沸により分
離する。その後、室温に冷却し、固液分離して水で充分
に洗浄し、減圧下40℃で30時間乾燥して平均粒径7
〜10μmのポリウレタンビーズを得た。Next, a separable flask equipped with a 2-liter stirrer was charged with 980 g of water, and 20 ml of methyl cellulose was added.
Dissolve 0 g to prepare a dispersion medium. 600r of this dispersion medium
While stirring at pm, 200 g of the above polyisocyanate prepolymer (I) and 200 g of polyurethane polypolymer polyol (II) were uniformly stirred and mixed, and the suspension was mixed with 60
The temperature is raised to 0 ° C. to react for 3 hours, then cooled to 52 ° C., 7 g of cellulolytic enzyme is added, the mixture is stirred for 30 minutes, then heated to 100 ° C., and toluene is azeotropically separated. Then, it was cooled to room temperature, solid-liquid separated, washed thoroughly with water, and dried under reduced pressure at 40 ° C. for 30 hours to obtain an average particle size of 7
Polyurethane beads of 10 μm were obtained.
【0014】得られたポリウレタンビーズ(以下、製造
例1という)について、動的粘弾性測定装置(レオメト
リックス社製RSAII)を用い、圧縮振動法で損失弾性
率E”及び貯蔵弾性率E’を求め、tanδ(=E”/
E’)を算出し、表1に記載した。なお、従来、化粧料
に配合されていた粉末、具体的にはタルク、マイカ、セ
リサイト、ナイロン粉末、シリコーン粉末、ポリスチレ
ン粉末について対応する値を比較のために記載した。With respect to the obtained polyurethane beads (hereinafter referred to as Production Example 1), the loss elastic modulus E ″ and the storage elastic modulus E ′ were measured by a compression vibration method using a dynamic viscoelasticity measuring device (RSAII manufactured by Rheometrics). Then, tan δ (= E ”/
E ′) was calculated and is shown in Table 1. Incidentally, the corresponding values of the powders conventionally blended in cosmetics, specifically, talc, mica, sericite, nylon powder, silicone powder, and polystyrene powder are shown for comparison.
【0015】[0015]
【表1】 [Table 1]
【0016】 〔実施例1〕 (1) ステアリン酸 2.4重量% (2) モノステアリン酸プロピレングリコール 2.0重量% (3) ベヘニルアルコール 0.2重量% (4) 液状ラノリン 2.0重量% (5) 流動パラフィン 8.0重量% (6) パラオキシ安息香酸プロピル 適量 (7) 精製水 64.5重量% (8) カルボキシメチルセルロースNa 0.2重量% (9) ベントナイト 0.5重量% (10)グリセリン 4.0重量% (11)トリエタノールアミン 1.1重量% (12)パラオキシ安息香酸メチル 適量 (13)酸化チタン 8.0重量% (14)着色顔料 適量 (15)ポリウレタンビーズ(製造例1) 5.0重量% (16)香料 適量 上記の成分(13)〜(15)を予め混合攪拌して得た整粒を、
成分(7) 〜(12)を加熱混合溶解した液体に添加し、攪拌
して均一にし、別途加熱混合溶解した成分(1)〜(6) を
添加し、乳化した。その後、冷却し、成分(16)を添加
し、攪拌して均一化して乳液状のファンデーションを得
た。得られたファンデーションを18℃の室内で使用し
たところ、塗布時の滑り感が良く、塗布後における密着
感及び使用感も優れ、違和感を全く感じなかった。Example 1 (1) Stearic acid 2.4 wt% (2) Propylene glycol monostearate 2.0 wt% (3) Behenyl alcohol 0.2 wt% (4) Liquid lanolin 2.0 wt% (5) Liquid paraffin 8.0 wt% (6) Propyl paraoxybenzoate (7) Purified water 64.5 wt% (8) Carboxymethylcellulose Na 0.2 wt% (9) Bentonite 0.5 wt% (10) ) Glycerin 4.0% by weight (11) Triethanolamine 1.1% by weight (12) Methyl paraoxybenzoate (13) Titanium oxide 8.0% by weight (14) Color pigment (15) Polyurethane beads (Production example) 1) 5.0 wt% (16) Fragrance Suitable amount The sized particles obtained by mixing and stirring the above components (13) to (15) in advance,
Components (7) to (12) were added to a liquid which was heated and mixed and dissolved, and the mixture was stirred to make it uniform. Separately, components (1) to (6) which were heated and mixed and dissolved were added and emulsified. Then, it cooled, added the component (16), stirred and homogenized, and obtained the emulsion base. When the obtained foundation was used in a room at 18 ° C., it had a good slippery feel during application, excellent adhesion and usability after application, and no discomfort.
【0017】 〔実施例2〕 (1) ポリウレタンビーズ(製造例1) 10.0重量% (2) 雲母チタン 20.0重量% (3) タルク 20.0重量% (4) セリサイト 15.0重量% (5) ステアリン酸マグネシウム 2.0重量% (6) 着色顔料 適量 (7) 流動パラフィン 8.0重量% (8) パラフィンロウ 1.5重量% (9) 防腐剤 適量 上記の成分(1) 〜(6) を予め混合攪拌して得た整粒を、
成分(7) 〜(9) を加熱混合溶解した液体に添加し、攪拌
して均一にし、これを金皿に充填して圧縮成形して固型
粉末状アイシャドウを得た。得られたアイシャドウを1
8℃の室内で筆で塗布したところ、塗布時の伸びの軽さ
があり塗布後における密着感及び使用感も優れ違和感を
全く感じなかった。[Example 2] (1) Polyurethane beads (Production Example 1) 10.0 wt% (2) Mica titanium 20.0 wt% (3) Talc 20.0 wt% (4) Sericite 15.0 % By weight (5) Magnesium stearate 2.0% by weight (6) Color pigment suitable amount (7) Liquid paraffin 8.0% by weight (8) Paraffin wax 1.5% by weight (9) Preservative suitable amount Above ingredients (1 ) ~ (6) in advance by mixing and stirring the sized,
Ingredients (7) to (9) were added to a liquid which was mixed by heating and dissolved, and the mixture was stirred to make it uniform, which was then filled in a gold plate and compression-molded to obtain a solid powdery eye shadow. 1 for the obtained eye shadow
When it was applied with a brush in a room at 8 ° C., the elongation during application was light, and the adhesion and use feeling after application were excellent and no discomfort was felt.
【0018】 〔実施例3〕 (1) ポリウレタンビーズ(製造例2) 50.0重量% (2) タルク 40.0重量% (3) 沈降炭酸カルシウム 5.0重量% (4) ステアリン酸マグネシウム 4.0重量% (5) 着色顔料 適量 (6) 防腐剤 適量 (7) 香料 適量 上記の成分(1) 〜(6) を予め混合攪拌して得た整粒を、
成分(7) を添加し、攪拌して均一にし、これを容器に充
填して粉おしろいを得た。得られた粉おしろいを18℃
の室内で塗布したところ、塗布時の伸びの軽さがあり、
塗布後における密着感及び使用感も優れ、違和感を全く
感じなかった。[Example 3] (1) Polyurethane beads (Production Example 2) 50.0 wt% (2) Talc 40.0 wt% (3) Precipitated calcium carbonate 5.0 wt% (4) Magnesium stearate 4 0.0% by weight (5) Coloring pigment Appropriate amount (6) Preservative Appropriate amount (7) Perfume Appropriate amount The above-mentioned components (1) to (6) are mixed and stirred to obtain a sized powder,
Ingredient (7) was added, and the mixture was stirred to make it uniform, and this was filled in a container to obtain a powder white powder. The obtained powder white powder is placed at 18 ℃
When applied in the room, there is a light extension during application,
The adhesiveness and the feeling of use after application were excellent, and no discomfort was felt.
【0019】[0019]
【発明の効果】本発明は、上記の構成を採用し、化粧料
に形状記憶性樹脂の球状微細粉体を配合し、そのガラス
転移点、ガラス転移点前後での弾性率比及び損失正接t
anδの適切な値に選択することにより、メイクアップ
化粧料の化粧時に滑り感及び伸びの軽さがあり、また、
塗布後の密着感、使用感の優れたメイクアップ化粧料を
提供することができるようになった。EFFECTS OF THE INVENTION The present invention adopts the above-mentioned constitution, and the spherical fine powder of the shape memory resin is blended in the cosmetic, and its glass transition point, the elastic modulus ratio before and after the glass transition point and the loss tangent t.
By selecting an appropriate value of an δ, there is a feeling of slippage and light elongation when applying makeup cosmetics, and
It has become possible to provide a makeup cosmetic having excellent adhesion and application feeling after application.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 林 俊一 愛知県名古屋市中村区岩塚町字高道1番地 三菱重工業株式会社名古屋研究所内 (72)発明者 藤井 政志 滋賀県八日市市岡田町112−1 株式会社 ノエビア内 (72)発明者 塩貝 芳樹 滋賀県八日市市岡田町112−1 株式会社 ノエビア内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Shunichi Hayashi No. 1 Takamichi, Iwazuka-cho, Nakamura-ku, Aichi Prefecture Nagoya, Mitsubishi Heavy Industries, Ltd. Nagoya Research Institute (72) Inventor Masashi Fujii 112-1 Okada-cho, Yokaichi-shi, Shiga Prefecture Noevir Co., Ltd. (72) Inventor Yoshiki Shiogai 112-1, Okada-cho, Yokaichi-shi, Shiga Noevia Co., Ltd.
Claims (4)
皮膚表面温度でガラス転移して弾性率が変化する形状記
憶樹脂よりなる球状の微細粉体を配合したことを特徴と
するメイクアップ化粧料。1. The glass transition point is lower than the skin surface temperature,
A make-up cosmetic composition comprising a spherical fine powder made of a shape memory resin, which changes its elasticity by glass transition at the skin surface temperature.
以上であり、皮膚表面温度近傍における損失正接tan
δが0.3〜0.9の範囲にある形状記憶性樹脂を用い
たことを特徴とする請求項1記載のメイクアップ化粧
料。2. The elastic modulus ratio before and after the glass transition point is 4
The above is the loss tangent tan near the skin surface temperature
The makeup cosmetic according to claim 1, wherein a shape-memory resin having δ in the range of 0.3 to 0.9 is used.
レタンであることを特徴とするメイクアップ化粧料。3. A makeup cosmetic, wherein the shape-memory resin according to claim 2 is polyurethane.
配合したことを特徴とする請求項1〜3のいずれか1項
に記載のメイクアップ化粧料。4. The shape memory resin is 0.01 to 80% by weight.
The make-up cosmetics according to any one of claims 1 to 3, wherein the make-up cosmetics are blended.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27813693A JPH07126125A (en) | 1993-11-08 | 1993-11-08 | Make-up cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27813693A JPH07126125A (en) | 1993-11-08 | 1993-11-08 | Make-up cosmetic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07126125A true JPH07126125A (en) | 1995-05-16 |
Family
ID=17593099
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27813693A Withdrawn JPH07126125A (en) | 1993-11-08 | 1993-11-08 | Make-up cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07126125A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10298033A (en) * | 1997-04-28 | 1998-11-10 | L'oreal Sa | Composition containing coating layer-forming fluorine polymer |
JP2000072624A (en) * | 1998-06-18 | 2000-03-07 | Kose Corp | Solid powdery cosmetic |
JP2002539231A (en) * | 1999-03-19 | 2002-11-19 | カラー アクセス,インコーポレイティド | Gel powder composition |
KR100588831B1 (en) * | 2005-02-01 | 2006-06-14 | 한불화장품주식회사 | The manufacturing method and cosmetics composition of shape-memory type hydrogel emulsions by associative polymers |
US8263057B2 (en) | 2006-12-18 | 2012-09-11 | Avon Products, Inc. | Mascara composition containing shape-memory polymers, gels, and fibers |
US8592034B2 (en) | 2009-06-16 | 2013-11-26 | 3M Innovative Properties Company | Debondable adhesive article |
US8763231B2 (en) | 2009-04-10 | 2014-07-01 | 3M Innovative Properties Company | Blind fasteners |
US8870236B2 (en) | 2009-11-16 | 2014-10-28 | 3M Innovative Properties Company | Pipe section joining |
US9422964B2 (en) | 2009-04-10 | 2016-08-23 | 3M Innovative Properties Company | Blind fasteners |
-
1993
- 1993-11-08 JP JP27813693A patent/JPH07126125A/en not_active Withdrawn
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10298033A (en) * | 1997-04-28 | 1998-11-10 | L'oreal Sa | Composition containing coating layer-forming fluorine polymer |
JP2000072624A (en) * | 1998-06-18 | 2000-03-07 | Kose Corp | Solid powdery cosmetic |
JP2002539231A (en) * | 1999-03-19 | 2002-11-19 | カラー アクセス,インコーポレイティド | Gel powder composition |
KR100588831B1 (en) * | 2005-02-01 | 2006-06-14 | 한불화장품주식회사 | The manufacturing method and cosmetics composition of shape-memory type hydrogel emulsions by associative polymers |
US8263057B2 (en) | 2006-12-18 | 2012-09-11 | Avon Products, Inc. | Mascara composition containing shape-memory polymers, gels, and fibers |
US8763231B2 (en) | 2009-04-10 | 2014-07-01 | 3M Innovative Properties Company | Blind fasteners |
EP2876309A1 (en) | 2009-04-10 | 2015-05-27 | 3M Innovative Properties Company | Blind fasteners |
US9422964B2 (en) | 2009-04-10 | 2016-08-23 | 3M Innovative Properties Company | Blind fasteners |
US8592034B2 (en) | 2009-06-16 | 2013-11-26 | 3M Innovative Properties Company | Debondable adhesive article |
US8870236B2 (en) | 2009-11-16 | 2014-10-28 | 3M Innovative Properties Company | Pipe section joining |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
A300 | Withdrawal of application because of no request for examination |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 20010130 |