JPS6037084B2 - Instant drying pack agent - Google Patents
Instant drying pack agentInfo
- Publication number
- JPS6037084B2 JPS6037084B2 JP11111378A JP11111378A JPS6037084B2 JP S6037084 B2 JPS6037084 B2 JP S6037084B2 JP 11111378 A JP11111378 A JP 11111378A JP 11111378 A JP11111378 A JP 11111378A JP S6037084 B2 JPS6037084 B2 JP S6037084B2
- Authority
- JP
- Japan
- Prior art keywords
- synthetic polyisoprene
- polyisoprene rubber
- pack
- weight
- film
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000001035 drying Methods 0.000 title claims description 14
- 229920003051 synthetic elastomer Polymers 0.000 claims description 50
- 229920000126 latex Polymers 0.000 claims description 39
- 229920001971 elastomer Polymers 0.000 claims description 37
- 239000005060 rubber Substances 0.000 claims description 37
- 239000003795 chemical substances by application Substances 0.000 claims description 34
- 230000008961 swelling Effects 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000012046 mixed solvent Substances 0.000 claims description 4
- 241000018344 Ehrlichia sp. 'CGE agent' Species 0.000 claims 1
- 239000004816 latex Substances 0.000 description 15
- -1 alkyl lithium Chemical compound 0.000 description 11
- 239000007788 liquid Substances 0.000 description 9
- 239000002585 base Substances 0.000 description 7
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 244000043261 Hevea brasiliensis Species 0.000 description 4
- 229920003052 natural elastomer Polymers 0.000 description 4
- 229920001194 natural rubber Polymers 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000001451 organic peroxides Chemical class 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- 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
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 206010040880 Skin irritation Diseases 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 2
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 229920006173 natural rubber latex Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 230000036556 skin irritation Effects 0.000 description 2
- 231100000475 skin irritation Toxicity 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- RZYIPLSVRHWROD-UHFFFAOYSA-N 1,2,4-trioxolane Chemical compound C1OCOO1 RZYIPLSVRHWROD-UHFFFAOYSA-N 0.000 description 1
- QYIMSPSDBYKPPY-BANQPHDMSA-N 2,3-epoxysqualene Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C=C(/C)CC\C=C(/C)CCC1OC1(C)C QYIMSPSDBYKPPY-BANQPHDMSA-N 0.000 description 1
- VQNCESOGPRGYLX-UHFFFAOYSA-N 2,4-dimethylpentan-3-one hydrogen peroxide Chemical compound OO.CC(C)C(=O)C(C)C VQNCESOGPRGYLX-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- PCNKKSQFXBISOR-UHFFFAOYSA-N 3-hydroperoxyhex-1-ene Chemical compound CCCC(OO)C=C PCNKKSQFXBISOR-UHFFFAOYSA-N 0.000 description 1
- CBNXGQUIJRGZRX-UHFFFAOYSA-N 5-[4-fluoro-3-(trifluoromethyl)phenyl]furan-2-carbaldehyde Chemical compound C1=C(C(F)(F)F)C(F)=CC=C1C1=CC=C(C=O)O1 CBNXGQUIJRGZRX-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- BGZKVDIFKPQYHL-UHFFFAOYSA-N C(C)(C)(C)OCOO Chemical compound C(C)(C)(C)OCOO BGZKVDIFKPQYHL-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- 241000234435 Lilium Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- PVMNBWXRCLEDCL-UHFFFAOYSA-N acetaldehyde;aniline Chemical compound CC=O.NC1=CC=CC=C1 PVMNBWXRCLEDCL-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 210000000245 forearm Anatomy 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- AILKHAQXUAOOFU-UHFFFAOYSA-N hexanenitrile Chemical compound CCCCCC#N AILKHAQXUAOOFU-UHFFFAOYSA-N 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- GSGDTSDELPUTKU-UHFFFAOYSA-N nonoxybenzene Chemical compound CCCCCCCCCOC1=CC=CC=C1 GSGDTSDELPUTKU-UHFFFAOYSA-N 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 230000037380 skin damage Effects 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0212—Face masks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- A61K8/8111—Homopolymers or copolymers of aliphatic olefines, e.g. polyethylene, polyisobutene; Compositions of derivatives of such polymers
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Description
【発明の詳細な説明】
本発明は加硫した合成ポリィソプレンゴムを皮膜形成剤
とする即乾性に富んだパック剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a quick-drying pack containing vulcanized synthetic polyisoprene rubber as a film-forming agent.
従来、パック剤の主流をなすものは、ポリビニルァルコ
ール等の水港性高分子を皮膜形成剤とする液状又はペー
スト状パック剤であった。Conventionally, the mainstream pack agents have been liquid or paste pack agents that use a water-portable polymer such as polyvinyl alcohol as a film-forming agent.
か)るパック剤は、皮膜形成剤を高濃度にすると粘度が
非常に高くなり、皮膚に塗布する際伸びが悪く塗布し‘
こくいので、通常は低濃度で使用しなければならず、こ
のため皮膜形成時の乾燥速度が遅く、特に夏期は発汗作
用のために乾燥速度が更に遅れるという欠点があった。
又パック後の使用済み皮膜を剥離するに際しては、該皮
膜と皮膚との密着性が良適ぎるため、皮膜に産毛がから
んだりして剥離時に痛みや引裂感などの強い皮膚刺激が
あり、或いは皮膜の強度が不十分なため、皮膜が破れた
り、皮膚に皮膜の一部が残存するなどの欠点があり、皮
膜の剥離除去も容易ではなかった。かかる欠点を改善或
いは除去するために、高分子ラテツクス或いはェマルジ
ョンを使用することが提案されており、例えば天然ゴム
或いはスチレンーブタジェンゴムなどの合成ゴムをラテ
ックス状にて高濃度で使用することにより、短時間で乾
燥してパックした皮膚上に強籾な皮膜を形成する即鞄性
パック剤が得れらることが知られている。しかしながら
、かかる天然ゴムラテックスは、安定剤としてアンモニ
アが配合されており、これが皮膚障害の原因となるため
、ラテックスの安定性を阻害させない方法で中和しなか
ればならない。又、天然ゴムは低モジュラスであり、且
つ皮膚との密着性が大きいため、皮膜剥離の際にゴム特
有の高伸長を起こし易く剥離が容易ではなく、更には皮
膜切断の原因ともなり切断して収縮したゴム片が皮膚面
を直撃して強い痛みを覚えるなどの欠点があった。一方
、合成ゴムは、天然ゴムと比較して親水性非ゴム成分を
含まないため吸水性が極めて低く、即鞍性に富んだパッ
ク剤が得られるが、天然ゴムが抱える低モジュラスに係
る上言己欠点は依然として改善できない。When the film-forming agent is used in a high concentration, the viscosity of the pack becomes very high, making it difficult to spread when applied to the skin.
Since it is thick, it usually has to be used at a low concentration, which has the disadvantage that the drying rate during film formation is slow, and especially in summer, the drying rate is further delayed due to the sweating effect.
In addition, when removing the used film after the pack, the adhesion between the film and the skin is too good, so downy hair gets entangled in the film, causing strong skin irritation such as pain and tearing sensation when peeling. Alternatively, because the strength of the film is insufficient, there are drawbacks such as the film being torn or a portion of the film remaining on the skin, and it is not easy to remove the film. In order to improve or eliminate such drawbacks, it has been proposed to use polymer latexes or emulsions. For example, by using natural rubber or synthetic rubber such as styrene-butadiene rubber in latex form at high concentration. It is known that a ready-to-bag pack agent can be obtained which dries in a short time and forms a tough film on the packed skin. However, such natural rubber latex contains ammonia as a stabilizer, which causes skin damage, so it must be neutralized in a way that does not impair the stability of the latex. In addition, natural rubber has a low modulus and has high adhesion to the skin, so when the film is peeled off, it tends to elongate to a high degree, which is characteristic of rubber, making it difficult to peel off. There were drawbacks such as the shrinking rubber pieces hitting the skin directly and causing severe pain. On the other hand, synthetic rubber has extremely low water absorption compared to natural rubber because it does not contain hydrophilic non-rubber components, and it is possible to obtain a pack agent with excellent saddle-ready properties. I still can't improve my own shortcomings.
更には、天然ゴムと比較して、非ゴム成分を含まないた
め極めて衛生的であると云われているが、ラテックスの
製造方法から容易に推察できるように、合成時の禾反応
モノマーが一部残存するため、該モノマーによる悪臭が
皮層障害の問題があり、未だ実用化されるには至ってい
ない。本発明者はか)る問題点を解決すべ〈鋭意研究の
結果、加硫した合成ポリィソプレンゴムがパック剤用の
卓越した皮膜形成剤であることを認め、本発明を完成し
た。Furthermore, compared to natural rubber, it is said to be extremely hygienic because it does not contain non-rubber components, but as can be easily inferred from the manufacturing method of latex, some of the reactive monomers during synthesis are Since the monomer remains, the foul odor caused by the monomer poses a problem of damage to the skin layer, and it has not yet been put to practical use. The inventors of the present invention have completed the present invention to solve these problems.As a result of intensive research, the present inventors have recognized that vulcanized synthetic polyisoprene rubber is an excellent film-forming agent for pack agents.
本発明の第一の目的は、遠乾・性に富んだパック剤を提
供するにある。The first object of the present invention is to provide a pack agent with excellent spin-drying properties.
第二の目的は、パック後の使用済み皮膜の剥離性が容易
なるパック剤を提供するにある。即ち、本発明は合成ポ
リィソプレンゴムラテックスを皮膜形成用基剤として含
有するパック剤であって、合成ポリィソブレンゴムが加
硫合成ポリィソプレンゴム単独、又は加硫合成ポリィソ
フ。The second object is to provide a pack agent that allows easy removal of the used film after packing. That is, the present invention is a pack agent containing synthetic polyisoprene rubber latex as a film-forming base material, wherein the synthetic polyisoprene rubber is vulcanized synthetic polyisoprene rubber alone or vulcanized synthetic polyisoprene rubber.
レンゴムと未加硫合成ポリィソプレンゴムとの混合物よ
りなり、230に於けるベンゼン/エタノール=2′1
(重量比)よりなる混合溶媒に対する膨欄度が200〜
260%であることを特徴とする則礎性パック剤である
。ここで、膨潤度とは、周知の如く、乾燥した高分子に
対する吸収された溶媒の重量比(%)であり、次式の如
く表わされる。Consisting of a mixture of polyurethane rubber and unvulcanized synthetic polyisoprene rubber, benzene/ethanol = 2'1 at 230
The degree of swelling for a mixed solvent consisting of (weight ratio) is 200~
260%. Here, the degree of swelling is, as is well known, the weight ratio (%) of the absorbed solvent to the dry polymer, and is expressed by the following formula.
勝因度(%)=準寿とX,。Winning factor (%) = Junior longevity and X.
。W,:乾燥した皮膜状試料の重量
W2:乾燥した皮膜状試料を、ベンゼンノェタノール;
2/1(重量比)からなる混合溶媒に25q0で2小寺
間浸潰した後、試料を取り出し、試料表面に付着してい
る溶媒を軽く除外した後の試料の重量
本発明に適用される合成ポリィソプレンゴムラテツクス
は、一般的には、アルキルリチウムなどのりチゥム系触
媒、又はトIJアルキルアルミニゥム−四塩化チタン系
などのチーグラー触媒によりアニオン重合された、シス
ー1,4結合が90%以上を示す未加硫合成ポリィソプ
レンゴムをラテックス状にし、該ラテックスを有機過酸
化物又はアゾビスニトリルにて、通常は加硫促進剤の存
在下に、加硫することにより得られるが、更には、か)
る加硫合成ポリィソプレンゴムラテックスと未加硫合成
ポリィソプレンゴムラテックスとの混合系にても本発明
に適用可能である。. W,: weight of the dried film-like sample W2: weight of the dried film-like sample, benzenoethanol;
Weight of the sample after being immersed in a mixed solvent of 2/1 (weight ratio) at 25q0 for 2 hours, taking out the sample, and lightly removing the solvent attached to the sample surface.Synthesis applied to the present invention Polysoprene rubber latex generally has 90 cis-1,4 bonds, which are anionically polymerized using a glue-based catalyst such as alkyl lithium or a Ziegler catalyst such as TJ alkyl aluminum-titanium tetrachloride system. % or more of unvulcanized synthetic polyisoprene rubber into latex form, and vulcanize the latex with organic peroxide or azobisnitrile, usually in the presence of a vulcanization accelerator. , and even)
A mixed system of vulcanized synthetic polyisoprene rubber latex and unvulcanized synthetic polyisoprene rubber latex can also be applied to the present invention.
上記の有機過酸化物としては、例えば、tert−プチ
ルヒド。Examples of the above-mentioned organic peroxides include tert-butylhydride.
ベルオキシド、1−ビニルブチルヒドロベルオキシド、
クメンヒドロベルオキシド、ジイソプロピルケトンヒド
ロベルオキシドなどの如きヒド。オキシド、ジーter
t−ブチルベルオキシド、にrt−ブチル−Q−クミル
ベルオキシド、スクアレンベルオキシドなどの如きベル
オキシド、1−オキシエチルヒドロベルオキシド、にr
tーブトキシメチルヒドロベルオキシド、2,2−ジ(
把rt−ブチルベルオキシ)ブタン、エチレンオゾニド
、シクロベンタノンベルオキシドなどの如きベルオキシ
誘導体、過酢酸、ベルオキシ安息香酸釘ert−ブチル
、ジベンソぐィルベルオキシド、ジィソプロピルベルオ
キシ炭酸ジェチルなどの如き過酸及びその誘導体などが
ある。又、上記のアゾビスニトリルとしては、例えば、
2,2′ーアゾビスイソブチロニトリル、1,1′アゾ
ビス−1ーシク。peroxide, 1-vinylbutyl hydroperoxide,
hydrides such as cumene hydroperoxide, diisopropyl ketone hydroperoxide, etc. oxide, ter
peroxides such as t-butyl peroxide, rt-butyl-Q-cumyl peroxide, squalene peroxide, 1-oxyethyl hydroperoxide,
t-butoxymethyl hydroperoxide, 2,2-di(
peroxy derivatives such as (rt-butylberoxy)butane, ethylene ozonide, cyclobentanone peroxide, etc.; These include peracids and their derivatives. In addition, examples of the above azobisnitrile include:
2,2'-azobisisobutyronitrile, 1,1'azobis-1-cyc.
へキサンニトリルなどがある。尚、含硫黄物による加硫
は、残留硫黄の除去が一般に困難であり、又加硫化物が
着色するので、好ましくない。又、上記の加硫促進剤と
しては、例えば、テトラエチレンベンタミンなどの如き
ポリアミン類、ジー0−トリルグアニジンなどの如きグ
アニジン類、アセトアルデヒドアンモニアなどの如きァ
ルデヒドアンモニア類、アセトアルデヒドアニリンなど
の如きアルデヒドアミン類などがある。Examples include hexanenitrile. Incidentally, vulcanization using a sulfur-containing material is not preferred because it is generally difficult to remove residual sulfur and the vulcanized product is colored. Examples of the vulcanization accelerator include polyamines such as tetraethylenebentamine, guanidines such as di-0-tolylguanidine, aldehyde ammonias such as acetaldehyde ammonia, and aldehydes such as acetaldehyde aniline. There are amines, etc.
上記方法にて得られた合成ポリィソプレンゴムラテック
スを本発明に係るパック剤に適用するに際しては、合成
ポリィソプレンゴムの25ooにおけるベンゼン/エタ
ノール=2/1(重量比)からなる混合溶媒に対する膨
潤度が200〜260%でなければならない。膨潤度が
200%未満であると皮膜形成能が悪くなり、乾燥固化
したパック剤を剥離する際にひび割れした部分で皮膜が
切断し一様に剥がすことができない。又、膨潤度が26
0%を越えると、パック後乾燥固化した皮膜と皮膚との
密着性が良過ぎるため、皮膜を剥離する際に、皮膚が引
張られて痛いのみならず、ゴム特有の高伸長を起こし剥
離が容易ではなく、無理に剥離を強行すると高伸長した
皮膜が途中で切断し、収縮した切断ゴム片が皮層面を直
撃して強い痛みを覚えるという欠点がある。好ましくは
、膨潤度が230〜250%である。又、本発明に係る
合成ポリイソプレンゴムとして、加硫合成と未加硫合成
ポリィソプレンゴムとの混合物でも、該混合物の膨潤度
が上記の200〜260%でれば適用可能であり、かか
る混合物においては、加稀合成ポリィソプレンゴムが少
なくとも2の重量%含有することが好ましい。When applying the synthetic polyisoprene rubber latex obtained by the above method to the pack agent according to the present invention, it is necessary to The degree of swelling must be between 200 and 260%. If the degree of swelling is less than 200%, the film-forming ability will be poor, and when the dry and solidified pack agent is peeled off, the film will be cut at the cracked parts and cannot be peeled off uniformly. Also, the degree of swelling is 26
If it exceeds 0%, the adhesion between the film that has dried and solidified after the pack and the skin will be too good, and when the film is peeled off, it will not only be painful because the skin will be stretched, but it will also cause the high elongation characteristic of rubber, making it easy to peel off. However, if the skin is forcibly peeled off, the highly elongated skin will break midway, and the shrunken cut rubber pieces will hit the skin directly, causing intense pain. Preferably, the degree of swelling is 230-250%. Furthermore, as the synthetic polyisoprene rubber according to the present invention, a mixture of vulcanized synthetic and unvulcanized synthetic polyisoprene rubber can also be applied as long as the degree of swelling of the mixture is 200 to 260%, and such Preferably, the mixture contains at least 2% by weight of diluted synthetic polyisoprene rubber.
加硫合成ポリィソプレンゴムが2の重量%未満であると
、未加硫合成ポリィソプレンゴムの特性が強くなり、パ
ック後に乾燥固化した皮膜と皮膚との密着力が強くなり
すぎ、皮膜を剥離する際に皮膚が引張られ痛いなどの欠
点が出てくる。更に好ましくは、加硫合成ポリィソプレ
ンゴムの混合物有量は少なくとも40重量%である。か
かる合成ポリィソプレンゴムは本発明のパック剤中にラ
テックス状にて含有されるが、ゴム固形分含有量として
パック剤中に30〜65重量%で調製すれば良い。If the amount of vulcanized synthetic polyisoprene rubber is less than 2% by weight, the characteristics of unvulcanized synthetic polyisoprene rubber will be strong, and the adhesion between the dried and solidified film and the skin after the pack will be too strong, causing the film to deteriorate. Disadvantages include the skin being stretched and painful when peeled off. More preferably, the mixture content of vulcanized synthetic polyisoprene rubber is at least 40% by weight. Such synthetic polyisoprene rubber is contained in the pack agent of the present invention in the form of a latex, and the rubber solid content may be adjusted to 30 to 65% by weight in the pack agent.
3の重量%未満であると、パック剤の粘度が低すぎ、皮
膚に塗布し1こくいばかりでなく、乾燥速度も遅くなる
。If the amount is less than 3% by weight, the viscosity of the pack will be too low, making it difficult to apply to the skin and also slowing down the drying rate.
一方、65重量%を越えると、パック剤の粘度が高すぎ
、乾燥速度が極端に遠くなり、皮膚に美麗に塗布できな
くなる。尚、合成ポリィソプレンラテックスの安定剤と
してアルカリが使用されている場合には、凝集防止のた
めに若干の非イオン界面活性剤を添加した後、該ラテッ
クス中に炭酸ガスを吹き込むことなどによって該ラテッ
クスのpHを8〜9にまで中和し、パック剤用基材とし
て使用することが好ましい。又、合成ポリィソプレンゴ
ムラテツクスを加硫処理する際に使用される有機過酸化
物が未反応のまま遊離しているおそれがある場合には、
亜硫酸ナトリウム等の化粧料に添加できる還元剤にて、
か)る未反応遊離有機酸化物を還元しておくことが好ま
しい。本発明に係るパック剤は、上記の如く、所定の膨
潤度を有する合成ポIJィソプレンゴムラテックスを皮
膜形成用基材として含有することを特徴とするもので、
その他の従釆通常使用されてきたパック剤用基材はすべ
て必要に応じ使用可能である。On the other hand, if it exceeds 65% by weight, the viscosity of the pack agent will be too high and the drying speed will be extremely slow, making it impossible to apply it beautifully to the skin. In addition, when an alkali is used as a stabilizer for synthetic polyisoprene latex, a small amount of nonionic surfactant is added to prevent agglomeration, and then carbon dioxide gas is blown into the latex. It is preferable to neutralize the pH of the latex to 8 to 9 and use it as a base material for a pack agent. In addition, if there is a risk that the organic peroxide used when vulcanizing synthetic polysoprene rubber latex may remain unreacted,
With reducing agents that can be added to cosmetics such as sodium sulfite,
It is preferable to reduce unreacted free organic oxides. As mentioned above, the pack agent according to the present invention is characterized in that it contains a synthetic poIJ isoprene rubber latex having a predetermined degree of swelling as a base material for film formation.
All other commonly used base materials for pack agents can be used as required.
かくして得られた本発明に係るパック剤は、著し〈即乾
性に富むばかりでなく、パック時の塗布も容易にして美
麗に仕上り、又パック後に乾燥固化すると強軸な皮膜を
形成し、且つ該皮膜を剥離する際にも痛みや引張感など
の強い皮膚刺激もなく、更には該剥離時にゴム特有の高
伸長や剥離途中での皮膜切断を起こすこともなく、皮膚
から乾燥固化した皮膜を、容易にしてスムーズに、皮膜
全量一気に剥離することができる。The thus obtained pack agent according to the present invention not only has excellent quick-drying properties, but also is easy to apply during the pack, giving a beautiful finish, and forms a strong film when dried and solidified after the pack. There is no strong skin irritation such as pain or tension when the film is peeled off, and there is no high elongation characteristic of rubber or breakage of the film during peeling, and the dry and solidified film can be removed from the skin. , the entire film can be peeled off easily and smoothly at once.
以下、本発明を実施例にて更に具体的に説明する。Hereinafter, the present invention will be explained in more detail with reference to Examples.
尚、実施例中のパック剤の乾燥速度は、前腕部の3肌×
3肌にパック剤を0.5タ塗布し、該パック剤が乾燥す
るまでの時間で示した。実施例 1
ロジン酸カリウム3夕を溶解したペンタン3k9中に、
シスー1,4結合が93%で数平均分子量が77万の固
形ポリイソプレンゴム240夕を熔解し、更にロジン酸
カリウム3夕を添加する。In addition, the drying speed of the pack agent in the example is 3 skin on the forearm x
3. The time required for the pack to dry after applying 0.5 ta of the pack to the skin is shown. Example 1 Potassium rosinate was dissolved in pentane 3k9,
A solid polyisoprene rubber having a number average molecular weight of 770,000 and having 93% of cis-1,4 bonds is melted, and potassium rosinate is further added thereto.
次いで、該溶液中に水蒸気を吹き込みながら液温を70
±2℃に保ちつつ、高速乳化機にて該溶液を乳化状態と
なし、且つ徐々にペンタンを蒸発させて水に置換した。
更に、該乳化液を30仇肋Hgの減圧下に24時間放置
し、残存するペンタンを除去した後、室温大気圧下で遠
心脱水し、固形分濃度が66重量%の未加硫合成ポリィ
ソプレンゴムラテックスを得た。得られた未加硫合成ポ
リィソブレンゴムの25℃におけるベンゼン/エタノー
ル:2′1(重量比)からなる混合溶媒に対する勝潤度
は270%であった。上記で得た未加硫合成ポリィソプ
レンゴムラテックス100のこ安定剤としてポリオキシ
ェチレン(EO:20モル付加)ノニルフェニルェーテ
ルを0.07#添加燭拝した後、4.0重量%のte比
ーブチルヒドロベルオキシド水溶液10夕と更に上記の
ポリオキシヱチレンノニルフエニルエーテル0.07夕
を加えて約1時間鷹拝を続ける。Next, while blowing water vapor into the solution, the temperature of the solution was lowered to 70°C.
While maintaining the temperature at ±2°C, the solution was made into an emulsified state using a high-speed emulsifier, and pentane was gradually evaporated and replaced with water.
Further, the emulsion was left under a reduced pressure of 30 mHg for 24 hours to remove residual pentane, and then centrifugally dehydrated at room temperature and atmospheric pressure to obtain an unvulcanized synthetic polyester with a solid content concentration of 66% by weight. A pre-rubber latex was obtained. The wettability of the resulting unvulcanized synthetic polyisoprene rubber at 25° C. with respect to a mixed solvent consisting of benzene/ethanol:2'1 (weight ratio) was 270%. The unvulcanized synthetic polyisoprene rubber latex 100 obtained above was added with 0.07 # of polyoxyethylene (EO: 20 moles added) nonyl phenyl ether as a stabilizer, and then 4.0 weight % Te ratio-butyl hydroperoxide aqueous solution for 10 minutes and the above-mentioned polyoxyethylene nonyl phenyl ether 0.07 hours were added and the mixture was continued for about 1 hour.
次いで6000に加熱し、25重量%のテトラエチレン
ベンタミン水溶液50夕を徐々に加えて6時間燈梓を行
った後、L−アスコルビン酸0.2夕を添加して未反応
のまま遊離しているtert−プチルヒドロベルオキシ
ドを還元した。而る後、遠心分離機に脱水して、固形分
濃度が6毎重量%の加硫合成ポリィソプレンゴムラテッ
クスを得た。得られた加硫合成ポリイソプレンゴムの上
記で表示した膨潤度は203%であった。更に、上記の
操作方法に準じて、第1表に示す如き膨潤度を有する各
種加硫合成ポIJィソブレンゴムラテツクスを得た。Next, the mixture was heated to 6,000 ℃, and after 50 minutes of a 25% by weight aqueous solution of tetraethylenebentamine was gradually added and heated for 6 hours, 0.2 hours of L-ascorbic acid was added to release it unreacted. tert-butyl hydroperoxide was reduced. Thereafter, the mixture was dehydrated using a centrifuge to obtain a vulcanized synthetic polyisoprene rubber latex having a solid content concentration of 6% by weight. The swelling degree of the obtained vulcanized synthetic polyisoprene rubber as indicated above was 203%. Further, according to the above-mentioned operating method, various vulcanized synthetic polyisoprone rubber latexes having swelling degrees as shown in Table 1 were obtained.
尚、これらラテツクスは、いるれも、固形分濃度が6亀
重量%になるよう調製した。かくして得た加硫合成ポリ
ィソプレンゴムラテックス各65.の重量部と上記のポ
リオキシェチレンノニルフェニルェーテル0.6重量部
を蝿梓混合してA液とした。All of these latexes were prepared to have a solid content concentration of 6% by weight. Each of the thus obtained vulcanized synthetic polyisoprene rubber latexes contained 65. and 0.6 parts by weight of the above-mentioned polyoxyethylene nonyl phenyl ether were mixed to prepare a liquid A.
一方、水14.1重量部に上記のポリオキシェチレンノ
ニルフェニルェーテル0.1重量部とp−ヒドロキシ安
息香酸メチル0.2重量部を溶解させた後、コロィダル
カオリン20.の重量部を分散混合させてB液とした。
而る後、A液にB液を鷹拝しながら添加し、両液を均一
に混合せしめて、合成ポリィソプレンゴムラテックスを
皮膜形成用基材として含有する各種パック剤を得た。第
一表には、パック剤に使用した合成ポリィソプレンゴム
の膨酒度、並びに得られたパック剤の乾燥速度と皮膜剥
離特性を示した。Separately, 0.1 part by weight of the above polyoxyethylene nonyl phenyl ether and 0.2 part by weight of methyl p-hydroxybenzoate were dissolved in 14.1 parts by weight of water, and then 20 parts by weight of colloidal kaolin. Parts by weight were dispersed and mixed to obtain liquid B.
Thereafter, Solution B was added to Solution A, and both solutions were mixed uniformly to obtain various pack agents containing synthetic polyisoprene rubber latex as a film-forming base material. Table 1 shows the degree of swelling of the synthetic polyisoprene rubber used in the pack agent, as well as the drying rate and film peeling properties of the resulting pack agent.
尚、比較対照のため、加硫合成ポリィソプレンゴムラテ
ックス成分を天然ゴムラテックス(ゴム固形分65%)
、又はスチレンブタジエンゴム(S.B.R)ラテツク
ス(固形分63%)に代替して実施例1と同様にパック
剤を調製し、更にビールオフ型の代表的パック剤として
ポリビニルアルコール(PVA)を皮膜形成剤とする市
販パック剤についても例示した。第1表
実施例 2
実施例1で得られた未加硫合成ポリイソプレンゴムラテ
ックスと膨潤度が203%の加硫合成ポリィソプレンゴ
ムラテックスとを、第2表に示す如き配合割合にて混合
し、次いで該混合ラテックスの各65.の重量部と実施
例1のポリオキシェチレンノニルフェニルェーテル0.
6重量部を蝿梓混合してA液とする以外は、実施例1と
全く同様にして、加硫合成ポリイソプレンゴムラテック
スと未加硫合成ポリィソプレンゴムラテックスとからな
る混合物を皮膜形成用基材として含有する各種パック剤
を得た。For comparison, the vulcanized synthetic polyisoprene rubber latex component was replaced with natural rubber latex (rubber solid content 65%).
Or, a pack agent was prepared in the same manner as in Example 1 by substituting styrene butadiene rubber (S.B.R.) latex (solid content 63%), and polyvinyl alcohol (PVA) was further used as a typical beer-off type pack agent. Examples of commercially available pack agents using the film-forming agent are also given. Table 1 Example 2 The unvulcanized synthetic polyisoprene rubber latex obtained in Example 1 and the vulcanized synthetic polyisoprene rubber latex with a swelling degree of 203% were mixed at the blending ratio shown in Table 2. and then each 65% of the mixed latex. and 0.0 parts by weight of the polyoxyethylene nonylphenyl ether of Example 1.
A mixture of vulcanized synthetic polyisoprene rubber latex and unvulcanized synthetic polyisoprene rubber latex was prepared for film formation in exactly the same manner as in Example 1, except that 6 parts by weight of lily was mixed to form liquid A. Various pack agents contained as base materials were obtained.
第2表には、混合合成ポリィソプレンゴムラテックスの
混合割合と、かかる混合合成ポリィソプレンゴムの膨潤
度、並びに得られたパック剤の皮膜剥離特性を示した。Table 2 shows the mixing ratio of the mixed synthetic polyisoprene rubber latex, the degree of swelling of the mixed synthetic polyisoprene rubber, and the film release characteristics of the obtained pack agent.
第2表実施例 3
実施例1で得られた未加硫合成ポリィソブレンゴムラテ
ックスと膨潤度が178%の加硫合成ポリィソプレンゴ
ムラテックスとを、第3表に示す如き配合割合にて混合
し、次いで該混合ラテツクスの各65.の重量部と実施
例1のポリオキシェチレンノニルフヱニルェーテル0.
6重量部を凝梓混合してA液とした。Table 2 Example 3 The unvulcanized synthetic polyisoprene rubber latex obtained in Example 1 and the vulcanized synthetic polyisoprene rubber latex having a swelling degree of 178% were mixed in the proportions shown in Table 3. 65. of each of the mixed latex. and 0.0 parts by weight of the polyoxyethylene nonyl phenyl ether of Example 1.
6 parts by weight were coagulated and mixed to obtain liquid A.
一方、水27.5重量部に上記ポリオキシェチレンノニ
ルフェニルェーテル0.2重量部p−ヒドロキシ安息香
酸メチル0.2重量部及びメチルセルロース1.5重量
部を溶解させた後、微粒子酸化チタン5.の重量部を分
散混合させてB液とした。On the other hand, after dissolving 0.2 parts by weight of the polyoxyethylene nonyl phenyl ether, 0.2 parts by weight of methyl p-hydroxybenzoate and 1.5 parts by weight of methyl cellulose in 27.5 parts by weight of water, fine particle oxidation was carried out. Titanium 5. Parts by weight were dispersed and mixed to obtain liquid B.
而る後、A液にB液を蝿拝しながら添加し、両液を均一
に混合せしめて、実施例2と同様の加硫合成ポリィソプ
レンゴムラテツクスと未加硫合成ポリィソプレンゴムラ
テックスとからなる混合物を皮膜形成用基材として含有
する各種剤を得た。第3表は、混合合成ポIJィソプレ
ンゴムラテックスの混合割合と、かかる混合合成ポリィ
ソプレンゴムの膨潤度、並びに得られたパック剤の皮膜
剥離特性を示した。第3表After that, liquid B was added to liquid A while stirring, and both liquids were mixed uniformly to form the same vulcanized synthetic polyisoprene rubber latex and unvulcanized synthetic polyisoprene rubber as in Example 2. Various agents containing a mixture of latex and latex as a base material for film formation were obtained. Table 3 shows the mixing ratio of the mixed synthetic polyisoprene rubber latex, the degree of swelling of the mixed synthetic polyisoprene rubber, and the film release characteristics of the obtained pack agent. Table 3
Claims (1)
剤として含有するパツク剤であつて、合成ポリイソプレ
ンゴムが加硫合成ポリイソプレンゴム単独、又は加硫合
成ポリイソプレンゴムと未加硫合成ポリイソプレンゴム
との混合物よりなり、25℃に於けるベンゼン/エタノ
ール=2/1(重量比)よりなる混合溶媒に対する膨潤
度が200〜260%であることを特徴とする即乾性パ
ツク剤。 2 パツク剤中における合成ポリイソプレンゴムラテツ
クスの固形分含有量が30〜65重量%である特許請求
の範囲第1項記載の即乾性パツク剤。 3 合成ポリイソプレンゴムの結合様式が少なくとも9
0%以上のシス−1,4結合からなるものである特許請
求の範囲第1項又は第2項記載の即乾性パツク剤。 4 加硫合成ポリイソプレンゴムと未加硫合成ポリイソ
プレンゴムとの混合物が加硫合成ポリイソプレンゴムを
少なくとも20重量%含有するもので特許請求の範囲第
1項乃至第3項の何れかに記載の即乾性パツク剤。[Scope of Claims] 1. A pack agent containing synthetic polyisoprene rubber latex as a film-forming base material, wherein the synthetic polyisoprene rubber is used alone or in combination with vulcanized synthetic polyisoprene rubber. A quick-drying pack made of a mixture with vulcanized synthetic polyisoprene rubber and characterized by a swelling degree of 200 to 260% in a mixed solvent of benzene/ethanol = 2/1 (weight ratio) at 25°C. agent. 2. The quick-drying pack according to claim 1, wherein the solid content of the synthetic polyisoprene rubber latex in the pack is 30 to 65% by weight. 3 The binding mode of the synthetic polyisoprene rubber is at least 9
The quick-drying pack according to claim 1 or 2, which comprises 0% or more of cis-1,4 bonds. 4. A mixture of vulcanized synthetic polyisoprene rubber and unvulcanized synthetic polyisoprene rubber containing at least 20% by weight of vulcanized synthetic polyisoprene rubber, as set forth in any one of claims 1 to 3. A quick-drying face pack.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11111378A JPS6037084B2 (en) | 1978-09-09 | 1978-09-09 | Instant drying pack agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11111378A JPS6037084B2 (en) | 1978-09-09 | 1978-09-09 | Instant drying pack agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5538317A JPS5538317A (en) | 1980-03-17 |
| JPS6037084B2 true JPS6037084B2 (en) | 1985-08-24 |
Family
ID=14552733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11111378A Expired JPS6037084B2 (en) | 1978-09-09 | 1978-09-09 | Instant drying pack agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6037084B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210131407A (en) * | 2019-03-29 | 2021-11-02 | 제이에프이 스틸 가부시키가이샤 | Steel plate for can and manufacturing method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6640795B2 (en) * | 2017-07-18 | 2020-02-05 | 株式会社ジャパンビューティプロダクツ | Cosmetics |
-
1978
- 1978-09-09 JP JP11111378A patent/JPS6037084B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210131407A (en) * | 2019-03-29 | 2021-11-02 | 제이에프이 스틸 가부시키가이샤 | Steel plate for can and manufacturing method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5538317A (en) | 1980-03-17 |
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