[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

JPH01319518A - Silicone/acrylic copolymer composition - Google Patents

Silicone/acrylic copolymer composition

Info

Publication number
JPH01319518A
JPH01319518A JP15155188A JP15155188A JPH01319518A JP H01319518 A JPH01319518 A JP H01319518A JP 15155188 A JP15155188 A JP 15155188A JP 15155188 A JP15155188 A JP 15155188A JP H01319518 A JPH01319518 A JP H01319518A
Authority
JP
Japan
Prior art keywords
formula
silicone
weight
film
group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP15155188A
Other languages
Japanese (ja)
Other versions
JP2638612B2 (en
Inventor
Yoji Yokoyama
横山 洋士
Yoshio Sasaki
佐々木 義雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissin Chemical Industry Co Ltd
Original Assignee
Nissin Chemical Industry Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=15520995&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JPH01319518(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Nissin Chemical Industry Co Ltd filed Critical Nissin Chemical Industry Co Ltd
Priority to JP63151551A priority Critical patent/JP2638612B2/en
Publication of JPH01319518A publication Critical patent/JPH01319518A/en
Application granted granted Critical
Publication of JP2638612B2 publication Critical patent/JP2638612B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

PURPOSE:To obtain the subject composition, having film-forming properties and providing the formed films excellent in surface characteristics by polymerizing a compound expressed by a specific formula with (meth)acrylic acid ester and carboxyl group-containing monoethylenically unsaturated monomer in respective prescribed proportions. CONSTITUTION:The objective composition obtained by polymerizing 10-60wt.% compound expressed by formula I [X is radically polymerizable group (optimally methacryloxy group); R<1> is 1-20C monofunctional hydrocarbon (optimally CH3), 1-20C monofunctional halogenated hydrocarbon or formula II (R<2> is 1-20C monofunctional hydrocarbon or monofunctional halogenated hydrocarbon; p is 5-100), provided that the number of a group expressed by formula III in R<1> is 0, 1 or 2; m is 1-10; n is 5-100] with (B) 25-75wt.% (meth)acrylic acid ester and (C) 5-20wt.% carboxyl group-containing monoethylenically unsaturated monomer [provided that the total amount of the component (A), (B) and (C) is 100wt.%] in the presence of a radical polymerization initiator and consisting essentially of a silicon/acrylic copolymer.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はシリコーン/アクリル共重合体の組成物に係わ
り、詳しくはアルコールなどの汎用の溶剤に溶解し弱ア
ルカリに膨潤する非架橋性のものて、他樹脂との相溶性
かよく、さらに、実用的な造膜性を有し形成された皮膜
は優れた表面特性を示すので、皮膜形成に有用とされる
シリコーン/アクリル共重合体を主成分として含有する
組成物に関するものである。
Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a silicone/acrylic copolymer composition, specifically a non-crosslinkable one that dissolves in general-purpose solvents such as alcohol and swells in weak alkalis. Silicone/acrylic copolymers, which are useful for film formation, are mainly used because they have good compatibility with other resins, have practical film-forming properties, and the films formed show excellent surface properties. It relates to a composition containing it as an ingredient.

(従来の技術) 汎用シリコーンオイルとしてジメチルポリシロキサンは
耐熱性、耐光性、耐水性、耐薬品性、潤滑性、撥水性、
非粘着性、消泡性にすくね、生理的不活性であって、産
業用、家庭用品、医薬、化粧品などに広く使用されてい
るか、液状である為に単独でフィルム形成能かない。低
級アルコール、グリコールなとの親水性溶媒に不溶解、
水にはどのようなpHても不溶解で単独では乳化もされ
ない。
(Conventional technology) As a general-purpose silicone oil, dimethylpolysiloxane has properties such as heat resistance, light resistance, water resistance, chemical resistance, lubricity, water repellency,
It is non-adhesive, anti-foaming, and physiologically inert, and is widely used in industrial, household products, medicine, cosmetics, etc., and because it is liquid, it cannot form a film on its own. Insoluble in hydrophilic solvents such as lower alcohols and glycols,
It is insoluble in water at any pH and cannot be emulsified by itself.

他の物質との相溶性か極めて乏しいため、均一混合困難
て又、配合組成物から分離、ブリートし、性能が経時変
化するのみならず、これと接触する固体表面へ移行する
。接触し行を受けた表面かシリコーンオイルの特性(ヌ
メリ感覚、滑り性、非接着2撥水性、非再塗布性等)を
嫌う場合は、いわゆるシリコーン汚染となる。特に巻物
にされる製品(壁紙、粘着テープ、包装材料等)では表
面処理層中のシリコーンオイルか巻物化によって裏面を
45染し、裏面に必要な性能(粘着性。
Because it has extremely poor compatibility with other substances, it is difficult to mix uniformly, and it separates and bleeds from the blended composition, causing not only its performance to change over time, but also to migrate to solid surfaces that come into contact with it. If the surface that has been in contact with the coating does not like the characteristics of silicone oil (slimy feel, slipperiness, non-adhesion, water repellency, non-reapplicability, etc.), this is so-called silicone contamination. In particular, for products that are made into rolls (wallpaper, adhesive tapes, packaging materials, etc.), the back side is dyed with 45 dyes using silicone oil in the surface treatment layer or rolled to give the back side the necessary performance (adhesiveness).

印刷性等)を悪化させる。シリコーンオイルか一旦付着
した表面からの完全除去は極めて困難であり、強力な溶
剤を使わねばならないため、強力溶剤に耐えないプラス
ティック基材からは除去出来ないし、水やアルコールを
使用出来ないことは、家庭においては極めて不便である
。シリコーンオイルの付着した面はほこりを付着させや
すく、又付着したほこりは除去しにくい。
printability, etc.). It is extremely difficult to completely remove silicone oil from surfaces once it has adhered, and requires the use of strong solvents, so it cannot be removed from plastic substrates that cannot withstand strong solvents, and water or alcohol cannot be used. This is extremely inconvenient at home. Surfaces coated with silicone oil tend to attract dust, and attached dust is difficult to remove.

一方、造膜性を有するシリコーン系ポリマーとしては、
従来からシリコーン系マクロマーとメタアクリル酸エス
テルなどをグラフ1〜共重合させたポリマーが知られて
いるか、これらは何れも塗料などを高耐候性にするとか
、粘着テープなどのl1lii型性を改善させるなどを
目的としたものであった。
On the other hand, silicone polymers with film-forming properties include
Polymers made by copolymerizing silicone macromers and methacrylic acid esters as shown in graph 1 have been known for some time, and these can make paints etc. highly weather resistant or improve the l1lii type properties of adhesive tapes etc. It was aimed at such things.

市販されているこの種ポリマーの多くは、アクリル/シ
リコーン共重合物の末端基を利用して、架橋させるもの
であり、架橋したものはアルコール類に溶解しなかった
Many commercially available polymers of this type utilize the terminal groups of acrylic/silicone copolymers to crosslink, and the crosslinked polymers do not dissolve in alcohols.

また、シリコーン分の多いポリマーではフィルムラ形成
シなくなり油状になるので、下地への付着性か悪くなっ
たり、静電気をおひやすく汚れが何着しやすくなり、そ
の除去も容易でなかった。
In addition, polymers with a high silicone content do not form a film and become oily, resulting in poor adhesion to the substrate, being susceptible to static electricity, and easily attracting dirt, which is difficult to remove.

(発明か解決しようとする課題) 本発明は上記の欠点を解決し、シリコーンオイルの持つ
表面特性(潤滑性、撥水性、非粘着性。
(Problems to be Solved by the Invention) The present invention solves the above-mentioned drawbacks and improves the surface properties of silicone oil (lubricity, water repellency, non-adhesiveness).

非再塗布性、安定性等)を十分に生かし、しかも単独で
フィルムを形成出来る。他物質基材へ適度の接着力を有
する。実用的て使用しやすい低級アルコールに可溶であ
り、基材面から除去しやすい。他物質との相溶性かあり
一般の高分子物質、又ジメチルポリシロキサンオイルと
相溶する。
It takes full advantage of the properties (non-reapplicability, stability, etc.) and can form a film by itself. It has moderate adhesive strength to other substrates. It is soluble in lower alcohols, making it practical and easy to use, and it is easy to remove from the substrate surface. Compatible with other substances, general polymer substances, and dimethylpolysiloxane oil.

他物質への接触し行(汚染)を起こさない。アミン、ア
ンモニア水などの弱アルカリで容易に膨潤し、基材から
除去出来る。シリコーンオイル塗布面よりもほこりが付
着しにくい。低級アルコールに不溶解、不分散のジメチ
ルポリシロキサンを低級アルコールに安定分散させる助
剤となり得る。
Avoid contact with other substances (contamination). Easily swells with weak alkalis such as amines and aqueous ammonia, and can be removed from the substrate. Dust is less likely to adhere to surfaces than silicone oil coated surfaces. It can be used as an auxiliary agent to stably disperse dimethylpolysiloxane, which is insoluble and non-dispersible in lower alcohols, in lower alcohols.

などの特性を兼備したシリコーン/アクリル共重合体を
主成分どする組成物を提供するためになされたものであ
る。
This was done in order to provide a composition whose main component is a silicone/acrylic copolymer that has the following characteristics.

(発明の構成) 本発明者らは上記の目的を達成するために鋭意研究を重
ねた結果、本発明者らの合成したシリコーン/アクリル
系共重合体がこの目的に適合する可能性があることを見
出し、この知見に基づいてさらに検討を重ねて本発明に
到ったのである。
(Structure of the Invention) As a result of extensive research by the present inventors to achieve the above object, it has been discovered that the silicone/acrylic copolymer synthesized by the present inventors may be suitable for this purpose. Based on this knowledge, they conducted further studies and arrived at the present invention.

本発明の組成物は上記の目的を達成するものであり、こ
れは (A)−形成 [式中、Xはラジカル重合性基、R1は炭素数1〜20
の1価炭化水素基、1価ハロゲン化炭化水素〜20の1
価炭化水素基または1価ハロゲン化炭化水素基の1種ま
たは2種以上の基、pは5〜100の整数である)て示
される基から選ばれる1種または2種以上の基、たたし
、−形式中のすへてのバ′\ は2個、mは1〜10の整数、口は5〜100の整数で
ある]て示される化合物    10〜60重量%(B
)  アクリル酸エステルまたはメタクリル酸エステル
              25〜75重量%および (C)カルボキシル基含有モノエチレン性不飽和単量体
               5〜20重量%(たた
し、(A)+(B)+(C)−100重量%)をラジカ
ル重合開始剤の存在下に重合させて得られるシリコーン
/アクリル共重合体を主成分としてなるものである。
The composition of the present invention achieves the above object, and is characterized by (A)-forming [where X is a radically polymerizable group and R1 has 1 to 20 carbon atoms]
monovalent hydrocarbon group, monovalent halogenated hydrocarbon ~ 1 of 20
One or more groups selected from the following groups (where p is an integer of 5 to 100), a valent hydrocarbon group or a monovalent halogenated hydrocarbon group; 10 to 60% by weight (B
) Acrylic acid ester or methacrylic acid ester 25 to 75% by weight and (C) carboxyl group-containing monoethylenically unsaturated monomer 5 to 20% by weight (Tap, (A) + (B) + (C) - The main component is a silicone/acrylic copolymer obtained by polymerizing 100% by weight) in the presence of a radical polymerization initiator.

本発明の組成物の主成分であるシリコーン/アクリル共
重合体を構成するモノマー成分のうち(A)成分は前記
のとおり一般式 %式% CH2−CH、CH2−CHOC−なとが例示される特 が、特に好ましいのは、メタクリロキシ基、アクリロキ
シ基である。mは大き過ぎるとシリコーン(オルガノポ
リシロキサン)の効果を妨げるのて1〜10の整数とさ
れるものであるが、代表的なのは3である。R1がけい
素を含まないときのR1としてはメチル基、エチル基、
フェニル基、トリフルオロプロピル基等が例示され、好
ましくはメチル基である。 R2としてはりい素を含ま
ないときのR1と同様の基が例示される。 R1か式オ
ルカッポリシロキサンが小さすきるとオルガノポリシロ
キサンが有する潤滑性、撥水性、非粘着性なとの特徴が
発揮されず、大きすぎるとアルコール可溶性、フィルム
形成性などの点て性能が低下するのでnおよびpはそれ
ぞれ5〜100の範囲とされるものである。そして(A
)成分のモノマーとしては次のものが例示される。
Among the monomer components constituting the silicone/acrylic copolymer that is the main component of the composition of the present invention, component (A) has the general formula % as described above. Particularly preferred are methacryloxy and acryloxy groups. If m is too large, the effect of the silicone (organopolysiloxane) will be hindered, so m is an integer from 1 to 10, but 3 is typical. When R1 does not contain silicon, R1 is a methyl group, an ethyl group,
Examples include a phenyl group, a trifluoropropyl group, and a methyl group is preferred. Examples of R2 include the same groups as R1 when it does not contain silicon. If the R1 formula orcap polysiloxane is too small, the characteristics of organopolysiloxane such as lubricity, water repellency, and non-adhesion will not be exhibited, and if it is too large, the performance will deteriorate in terms of alcohol solubility, film forming properties, etc. Therefore, n and p are each in the range of 5 to 100. And (A
) The following are exemplified as monomers of the component.

II        jl 0      11Jb   CH3 E+t+ 3C)13 cl2−cl  OCCH25l−−コO5t〒cH3
(n−20)0      C83CI+3 al13CI+3 CH2−CH−C117Si←05ih「Cll3  
    (n−25)CH3CH3 (A)成分は、共重合体にポリシロキサンか持つ長所を
付与するが、少な過ぎればこの長所か不十分になり、多
過ぎれば造膜性、相溶性、他物質との密着性を失うので
(A)〜(C)成分全量のうち10〜60重量%とする
ことか必要である。
II jl 0 11Jb CH3 E+t+ 3C) 13 cl2-cl OCCH25l--koO5t〒cH3
(n-20)0 C83CI+3 al13CI+3 CH2-CH-C117Si←05ih "Cll3
(n-25) CH3CH3 Component (A) gives the copolymer the advantages that polysiloxane has, but if it is too small, these advantages will be insufficient, and if it is too large, it will improve film-forming properties, compatibility with other substances, etc. Since the adhesion of components (A) to (C) is lost, it is necessary to set the amount to 10 to 60% by weight of the total amount of components (A) to (C).

(B)成分はアクリル酸エステルまたはメタクリル酸エ
ステルであるか、そのアルコール成分として炭素数1〜
18のアルキル基またはアルコキシ置換アルキル基のも
のか用いられ、具体的にはアクリル酸又はメタクリル酸
のメチル、エチル、プロピル、ブチル、ヘキシル、シク
ロヘキシル、2エチルヘキシル、メトキシエチル、メト
キシブチルの各アルコールとのエステル等が例示される
Component (B) is an acrylic ester or methacrylic ester, or its alcohol component has 1 to 1 carbon atoms.
18 alkyl groups or alkoxy-substituted alkyl groups are used, specifically, acrylic acid or methacrylic acid with methyl, ethyl, propyl, butyl, hexyl, cyclohexyl, 2-ethylhexyl, methoxyethyl, and methoxybutyl alcohols. Examples include esters.

(B)成分は共重合体に溶剤溶解性、造膜性、相溶性、
他物質との接着性をあたえ、又皮膜の側梁軟性を広く調
節出来る。(B)成分の(メタ)アクリル酸エステルは
オルガノポリシロキサンが持つ優れた耐熱、耐光性を損
なうことかない。この(B)成分の特性を生かし、他の
有用な特性を損なわないようにするため、(B)成分の
量は(八)〜(C)成分全量のうち25〜75重景%と
貴重ことか必要である。
Component (B) has solvent solubility, film-forming properties, compatibility with the copolymer,
It provides adhesion to other materials and allows the flexibility of the coating to be adjusted over a wide range. The (meth)acrylic acid ester of component (B) does not impair the excellent heat resistance and light resistance of the organopolysiloxane. In order to take advantage of the properties of this component (B) and not impair other useful properties, the amount of component (B) must be 25 to 75% of the total amount of components (8) to (C). or is necessary.

(C)成分はカルホキシル基含有モノエチレン性不飽和
単量体であるか、これにはアクリル酸、メタクリル酸、
クロ)−ン酸、イタコン酸、マレイン酸、フマル酸、マ
レイン酸半エステル、フマル酸半エステル等が例示され
る。
Component (C) is a carboxyl group-containing monoethylenically unsaturated monomer, including acrylic acid, methacrylic acid,
Examples include chronic acid, itaconic acid, maleic acid, fumaric acid, maleic acid half ester, and fumaric acid half ester.

(C)成分は(B)成分と同様の機能を持つほか、基材
への接着力を更に増し、帯電性を低め、アミン、アンモ
ニア水などの弱アルカリへの膨潤乃至分散性を与えるこ
とにより、共重合体の除去性を更に容易にするものであ
る。多過ぎれば撥水性。
In addition to having the same functions as component (B), component (C) further increases adhesive strength to the base material, lowers charging properties, and provides swelling or dispersibility in weak alkalis such as amines and aqueous ammonia. , which further facilitates the removability of the copolymer. Too much water repellency.

耐水性を減し、皮膜が硬くなるので、この(C)成分の
量は(A)〜(C)成分全量のうち5〜20重量%とす
ることが必要である。
The amount of component (C) needs to be 5 to 20% by weight of the total amount of components (A) to (C), since it reduces water resistance and makes the film hard.

本発明で用いるシリコーン/アクリル共重合体には上記
(A)〜(C)成分以外のモノマーを共重合させること
もてきる。すなわち、塩化ビニル、スチレン、アクリロ
ニトリル、塩化ビニリデン、酢酸ビニル、2ヒドロキシ
エチルメタクリレート。
The silicone/acrylic copolymer used in the present invention can also be copolymerized with monomers other than the above-mentioned components (A) to (C). namely, vinyl chloride, styrene, acrylonitrile, vinylidene chloride, vinyl acetate, and 2-hydroxyethyl methacrylate.

Nメチロールアクリルアミド、アクリルアミ]・。N-methylol acrylamide, acrylamide]・.

グリシジルメタアクリレートなどのビニル単量体を更に
共重合させることも当然可能である。しかし本発明の趣
旨を損なわない為に、(A) 、 (B) 、 (C)
成分合計量100重量部に対し、20重量部以下が望ま
しい。
Of course, it is also possible to further copolymerize vinyl monomers such as glycidyl methacrylate. However, in order not to spoil the spirit of the present invention, (A), (B), (C)
The amount is preferably 20 parts by weight or less based on 100 parts by weight of the total amount of components.

本発明で用いるシリコーン/アクリル共重合体を合成す
るための共重合にはラジカル重合開始剤をもちい、溶液
重合又は懸濁重合か用いられる。
For copolymerization to synthesize the silicone/acrylic copolymer used in the present invention, a radical polymerization initiator is used, and either solution polymerization or suspension polymerization is used.

共重合方法自体は公知の方法てよい。ラジカル重合開始
剤はジヘンゾイルパ−オキサイト、キュメンハイドロパ
ーオキサイド、ジイソプロピルパーオキシカーボネート
、アゾビスイソブチロニトリル等が例示される。溶液重
合時の使用溶剤はメタノール、エタノール、イソプロパ
ツール、アセトン、メヂルエヂルケトン、酢酸エチル、
ヘンゼン、トルエン、エチレングリコールモノアルキル
エーテル等、懸濁重合ではポリビニルアルコール、メチ
ルセルロース等の高分子保護コロイドか懸濁剤として用
いられる。
The copolymerization method itself may be a known method. Examples of the radical polymerization initiator include dihenzoyl peroxide, cumene hydroperoxide, diisopropyl peroxycarbonate, and azobisisobutyronitrile. Solvents used during solution polymerization include methanol, ethanol, isopropanol, acetone, methyl edyl ketone, ethyl acetate,
In suspension polymerization, polymeric protective colloids such as polyvinyl alcohol and methylcellulose are used as suspending agents, such as Hensen, toluene, and ethylene glycol monoalkyl ether.

本発明の組成物は溶液状て使用するのが便利である。溶
液重合量はそのまま用いるか、又は水。
The compositions of the invention are conveniently used in solution form. The solution polymerization amount can be used as is or water.

エチレングリコール等で共重合物を析出し、洗浄、精製
、乾燥後溶剤に再度溶解する。懸濁重合量は水洗乾燥後
溶剤に溶解する。溶剤は家庭用品】 2 としての応用では、エタノール、イソプロパツールが衛
生上好ましい。他種ポリマーの改質剤として該ポリマー
溶液へ添加する場合は、該ポリマーの良溶媒を用いる。
The copolymer is precipitated with ethylene glycol or the like, washed, purified, dried, and then redissolved in a solvent. The suspension polymerized amount is dissolved in a solvent after washing with water and drying. [Solvents are household products] 2 For applications as solvents, ethanol and isopropanol are preferred from a sanitary standpoint. When added to the polymer solution as a modifier for other polymers, a good solvent for the polymer is used.

さらに、本発明で用いるシリコーン/アクリル共重合体
は、(C)成分に由来するカルボキシル基が用途により
アミン、アンモニアで中和されることも大きな特徴の一
つである。(C)成分を用いた未中和量は、例えはプラ
スティック、フィルム。
Furthermore, one of the major features of the silicone/acrylic copolymer used in the present invention is that the carboxyl group derived from component (C) can be neutralized with amine or ammonia depending on the use. The unneutralized amount using component (C) is, for example, plastic or film.

来月、金属等の基材ヘコーティングした場合、基材との
密着力がすぐれ、撥水性、耐水性であるに拘らず、アミ
ン、アンモニアなどの弱アルカリ水て処理すれば皮膜は
膨潤して基オAから剥離し、完全に除去できる。従って
、基材の汚れ防止や保護剤、艶出剤等の応用には未中和
量が好適である。
Next month, when coating a substrate such as metal, the coating will swell if treated with weak alkaline water such as amine or ammonia, regardless of its excellent adhesion to the substrate, water repellency, and water resistance. It can be peeled off from the base A and completely removed. Therefore, the unneutralized amount is suitable for use in preventing stains on substrates, as a protective agent, as a polishing agent, and the like.

一方、中和品からの皮膜は、特に高沸点アミンで中和し
た溶液からの皮膜は中性水で膨潤し基材から剥離除去さ
れるので医薬、化粧品で人体から容易に除くには中和品
が便利である。中和、未中和は本発明を限定するもので
はなく用途に応じて使用溝の選択に任される。
On the other hand, films from neutralized products, especially those from solutions neutralized with high-boiling amines, swell with neutral water and are peeled off from the base material, so they cannot be easily removed from the human body in pharmaceuticals and cosmetics. The products are convenient. Neutralization or non-neutralization does not limit the present invention and is left to the selection of the groove to be used depending on the application.

また、本発明の組成物に、染料、顔料やシリカ等の充填
剤、あるいは他の添加剤を配合することは本発明の目的
を損なわない限り任意である。
Furthermore, dyes, pigments, fillers such as silica, or other additives may be added to the composition of the present invention as long as they do not impair the purpose of the present invention.

本発明の組成物は種々の用途に有用であり、形成された
皮膜はシリコーンのようにほこりが付着せず、例えば、
塩ビ壁紙の汚れ防止、家具、自動車なとの汚れ防止と静
電気対策に利用でき、繊維表面などへの潤滑性付与(す
へすへした感覚)、塗料ラッカーなどへの利用、医薬、
化粧品などの基材及び被覆材などに利用することか出来
る。
The composition of the present invention is useful in a variety of applications, and the film formed does not attract dust like silicone, for example,
It can be used to prevent stains on PVC wallpaper, to prevent stains on furniture and automobiles, and to prevent static electricity.It can be used to provide lubricity to fiber surfaces (smooth feeling), to paint lacquer, etc., and to prevent stains on furniture and automobiles.
It can be used as base materials and covering materials for cosmetics, etc.

塩ビなとて作られた壁紙は広く実用されているか、静電
気を持つ為に汚れが付着しやすく、種々の静電気防止剤
か使用されているか満足なものは見られない。又、マジ
ックインキなどが付着した場合、これを十分に拭い去る
ことか出来なかった。つまり汚れか付着せず、仮に汚れ
が付着した場合でも拭き取りやすい壁紙の出現が望まれ
ていた。これは車に壁紙に限定されず、プラスティック
又は金属製品に本組成物をコーティングすることにより
、容易に望ましい性質を付与することか可能になる。す
なわち、台所用品(換気扇、冷蔵庫、電子レンジ、食器
棚などの厨房機器)などの油、はこり汚れを除去しやす
い。
Wallpaper made from PVC is not widely used, but because it has static electricity, dirt tends to stick to it, and various anti-static agents have been used, but none have been found to be satisfactory. Furthermore, if marker ink or the like adheres to the surface, it cannot be wiped off sufficiently. In other words, there was a desire for a wallpaper that would not only attract dirt, but even if it did get dirty, it would be easy to wipe it off. This is not limited to car wallpaper, but by coating plastic or metal products with the composition, desirable properties can be easily imparted. In other words, it is easy to remove oil and dirt from kitchen utensils (ventilation fans, refrigerators, microwave ovens, kitchen equipment such as cupboards), etc.

家庭用品の汚染保護剤としては、エタノール溶液にして
適用すれは、食用油2油ミスト、食品(グツチャツプ。
As a contamination protection agent for household products, it can be applied in the form of an ethanol solution, edible oil 2 oil mist, and food (gutschup).

ソース、醤油等)インキ、クレヨン、マジックインキ等
の汚れが着きにくく、或いは除去しやすい。適当な時間
後に、弱アルカリ水又はエタノール程度で塗膜を完全に
除去出来るし、シリコーンのようにほこりかイ」着しな
い。
Stain from ink (sauce, soy sauce, etc.), crayon, marker ink, etc. is difficult to adhere to or is easy to remove. After an appropriate amount of time, the paint film can be completely removed with weak alkaline water or ethanol, and unlike silicone, it does not attract dust.

本組成物は十分なフィルム形成能力を持っているので、
その他の家具製品、ブラインド類、自動車などの車両製
品のプラスティック部分またはガラス部分にもコーティ
ングして、効果を期待することが出来る。ジメチルポリ
シロキサンとの相溶性を利用してカーワックス製造にも
有用である。
Since this composition has sufficient film-forming ability,
It can also be applied to other furniture products, blinds, and plastic or glass parts of vehicle products such as automobiles to expect the effect. It is also useful for producing car wax by utilizing its compatibility with dimethylpolysiloxane.

医薬錠剤、顆粒などにも従来から、単なるアクリル系ポ
リマーをコーティングした例はあるが、本組成物による
コーティングでは、汚れか付着せず、透明で丈夫なフィ
ルムコーティングを可能にし、潤滑性のよいことは医薬
の製造、包装工程をも容易にする利点かある。化粧品の
場合でも、感触か良く、石鹸で除去可能なので、これら
の性能は多くの利用分野を可能とした。医薬化粧品の場
合、特にエタノール又は水/エタノール混合溶剤に溶け
、しかも透明なフィルムを形成することが望まれていた
か本発明により可能となった。
Pharmaceutical tablets, granules, etc. have been coated with simple acrylic polymers in the past, but coating with this composition allows for a transparent and durable film coating, with only dirt attached, and has good lubricity. This has the advantage of facilitating the manufacturing and packaging process of pharmaceuticals. Even in the case of cosmetics, these properties have enabled many fields of application, as they are pleasant to the touch and can be removed with soap. In the case of pharmaceutical and cosmetic products, it has been particularly desired to form a transparent film that is soluble in ethanol or a mixed solvent of water/ethanol, and has been made possible by the present invention.

勿論、他の樹脂との配合も容易で、塗料、特にシェラツ
クニス、エチルセルロース、ヒドロキシプロピルセルロ
ース等アルコール可m 性fil 脂のニス、ラッカー
への添加により塗膜の潤滑性付与等、性能改善に有用で
ある。
Of course, it can be easily blended with other resins, and is useful for improving performance, such as adding lubricity to paint films, by adding it to paints, especially alcohol-based varnishes and lacquers such as shellac varnish, ethyl cellulose, and hydroxypropyl cellulose. be.

これらの性能は各分野て望まれていながら、これまで十
分に実現しなかったものであるか、本発明によって可能
となったものである。
Although these performances are desired in various fields, they have not been fully realized until now, or they have been made possible by the present invention.

つきに本発明の実施例をあげる。Examples of the present invention will now be described.

実施例 [シリコーン/アクリル共重合体の合成と組成物の調製
] イソプロパノール中の溶液重合で、アセチルパーオキサ
イドを触媒として、第1表のモノマー組成で共重合体を
製造した。
Example [Synthesis of silicone/acrylic copolymer and preparation of composition] A copolymer was produced with the monomer composition shown in Table 1 by solution polymerization in isopropanol using acetyl peroxide as a catalyst.

攪拌機付密閉型反応器を窒素置換し、イソプロパツール
150重量部を仕込み反応器内を70tに調節したのぢ
アセチルパーオキサイF1.25重量部を添加し、つい
て下記のモノマーの混合物MAst (構造式は第1表
のとおり)   50重量部メタクリル酸メチル   
     20重量部アクリル酸エチル       
  20重量部メタクリル酸           1
0重量部を4時間にわたって添加した。添加終了後反応
器内を80℃に維持し5時間攪拌を続は反応を完結さゼ
た。
A closed reactor equipped with a stirrer was purged with nitrogen, 150 parts by weight of isopropanol was charged, and the inside of the reactor was adjusted to 70 tons. 1.25 parts by weight of acetyl peroxy F was added, and the following monomer mixture MAst ( Structural formula is as shown in Table 1) 50 parts by weight Methyl methacrylate
20 parts by weight ethyl acrylate
20 parts by weight methacrylic acid 1
0 parts by weight were added over 4 hours. After the addition was completed, the inside of the reactor was maintained at 80°C and stirred for 5 hours to complete the reaction.

ミキサーに40℃の温水1000重量部を入れ、せん断
攪拌しながら上記反応溶液を徐々に添加してポリマーを
析出させろ過した。再ひミキサー中に40℃の温水10
00重量部とろ過したポリマーを入れ、10分間せん断
攪拌したのちろ過した。これを3回繰返してからポリマ
ーを乾燥した。ポリマー収率は94%であった。このポ
リマーをエタノールに30%の濃度で溶解させて微黄色
はとんど透明の溶液S−1を得た。
1000 parts by weight of 40°C warm water was placed in a mixer, and the reaction solution was gradually added to the mixer while stirring with shear to precipitate the polymer, which was then filtered. Re-chill warm water at 40°C in a mixer for 10 minutes.
00 parts by weight and the filtered polymer were added, stirred with shear for 10 minutes, and then filtered. This was repeated three times and then the polymer was dried. Polymer yield was 94%. This polymer was dissolved in ethanol at a concentration of 30% to obtain a slightly yellow but almost transparent solution S-1.

同様にしてS−2、S−3を調製した。S-2 and S-3 were prepared in the same manner.

比較例として第1表に併記したようなオルガノポリシロ
キサンを含有しない共重合体を実施例と同様にして合成
し、実施例と同しく30%エタノール溶液(S−比−1
)を調製した。
As a comparative example, a copolymer containing no organopolysiloxane as listed in Table 1 was synthesized in the same manner as in the example, and a 30% ethanol solution (S-ratio -1) was synthesized in the same manner as in the example.
) was prepared.

第1表 *MASi;片端メタアクリロキシプロピル変性シメヂ
ルボリシロキサン CH3CH3CI+3 1       1   I C)I2−C−C−0−]]CH2+7Si−−HO5
i−7−CH3n−25Q            C
H3Cl、3[組成物の評価] 溶液S−1を用いて次の1〜7の試験を行った。
Table 1 *MASi; One-end methacryloxypropyl-modified cymedylbolysiloxane CH3CH3CI+3 1 1 I C)I2-C-C-0-]]CH2+7Si--HO5
i-7-CH3n-25Q C
H3Cl, 3 [Evaluation of composition] The following tests 1 to 7 were conducted using solution S-1.

結果についても併記する。The results are also listed.

1 造膜性;清浄なガラス板、アルミ板、ポリエチレン
グリコールテレフタレート(略称PET)フィルムにド
クターナイフをもちい、固形分5 g/m2になるよう
塗布し、常温自然乾燥した。透明で粘着感なく、滑性あ
る光沢の良いちみつな皮膜を形成した。
1. Film-forming property: Using a doctor knife, the film was applied to a clean glass plate, aluminum plate, or polyethylene glycol terephthalate (abbreviated as PET) film to a solid content of 5 g/m2, and then air-dried at room temperature. Formed a transparent, non-sticky, smooth, glossy honey film.

2、密着性;上記皮膜にセロテープを圧着し、急速に引
き離したが、皮膜は全く剥離しなかった。
2. Adhesion: Cellotape was pressed onto the above film and rapidly pulled off, but the film did not peel off at all.

3、耐ブロッキング性。3. Blocking resistance.

上記PETフィルム塗布品を塗膜同士合わせ、0.5k
g/cm2の荷重をかけ、湿度90%150℃の恒温恒
温器に24時間放置後、両面を剥がしたところ、容易に
はがれ、皮膜に全く異常がなかった。
Combine the above PET film coated products together, 0.5k
After applying a load of g/cm2 and leaving it in a constant temperature chamber at 150°C and 90% humidity for 24 hours, both sides were peeled off, and there was no abnormality in the film.

4 撥水性、上記ガラス板塗布品についてJIS−L−
1092による撥水性試験を行ったところ撥水度90で
あった。
4 Water repellency, JIS-L- for the above glass plate coated product
A water repellency test using 1092 was conducted and the water repellency was 90.

5 他物への移行性、上記ガラス板塗布品に、他の清浄
ガラス板をのせ、耐ブロッキング性と同条件て放置後、
そのカラス板を取り出した。そのガラス面はイ5わが全
くなく、又水を滴下すると試験前と同様に水はガラス面
をよく濡らして広がフた。以上から本発明品の皮膜は他
物を接触汚染しないことが分かる。
5. Migration to other objects: After placing another clean glass plate on the coated glass plate and leaving it under the same conditions as the anti-blocking property,
I took out the crow board. The glass surface had no scratches at all, and when water was dropped, the water thoroughly wetted the glass surface and spread out, just as before the test. From the above, it can be seen that the film of the product of the present invention does not contaminate other substances by contact.

6 はこりイ」着と除去、電気掃除器の集塵袋のほこり
を上記ガラス板塗布品に散布した。乾いたガーゼでふく
と、殆とほこりは除去され、濡れたガーゼでは完全に除
去された。
6. Dust from the dust collection bag of a vacuum cleaner was sprinkled on the glass plate coated product. Wiping with dry gauze removed most of the dust, and wiping with wet gauze removed it completely.

7 塗布膜の除去性、上記PETフィルム塗布品に、2
%アンモニア水、エタノールを滴下し、皮膜の除去性を
観察した。アンモニア水では2分後に皮膜か剥出(I膨
潤し布で容易に完全除去された。
7 Removability of coating film, 2
% ammonia water and ethanol were added dropwise, and the removability of the film was observed. When using ammonia water, the film peeled off (swelled) after 2 minutes and was easily and completely removed with a cloth.

エタノールには2分後に溶解し、布で完全に除去された
It dissolved in ethanol after 2 minutes and was completely removed with a cloth.

S−2,5−3,S−比−1についても上記1〜7の試
験を行ない、第2表の結果を得た。
Tests 1 to 7 above were also conducted for S-2, 5-3, and S-ratio-1, and the results shown in Table 2 were obtained.

第  2 表 S−1,S−2,5−3,5−比−1について次の8〜
10の試験を行なった。
2 Regarding Table S-1, S-2, 5-3, 5-ratio-1, the following 8~
Ten tests were conducted.

8゜ ジメチルポリシロキサンオイルのエタノール可溶
化、ジメチルポリシロキサン(信越化学工業(株)裂開
品名KF96.100cs) lOgにS−1,S−2
,S−3゜S−比−1各90gを混合し、静置5日後の
分離のイj無を観察した。結果は第3表のとおりてあっ
た。
8゜ Ethanol solubilization of dimethylpolysiloxane oil, dimethylpolysiloxane (Shin-Etsu Chemical Co., Ltd. splitting product name KF96.100cs) S-1, S-2 in lOg
, S-3°S-Ratio-1, 90 g each, were mixed and observed for separation after 5 days of standing. The results are shown in Table 3.

第  3  表 9 イ5染防止性;白色塩ビ壁紙にS−1,S−2,S
−3゜S−比−1を固形分換算587m2塗布し、 1
05℃×2分乾燥後、 220℃×2分熱処理した。粘
着感なく潤滑性ある表面か得られた。これに水性ペン(
黒)。
Table 3 9 A5 Dyeing prevention property; S-1, S-2, S on white PVC wallpaper
-3゜S-ratio-1 was applied to 587m2 in terms of solid content, and 1
After drying at 05°C for 2 minutes, it was heat-treated at 220°C for 2 minutes. A lubricated surface was obtained without any sticky feeling. Add this to a water-based pen (
black).

油性ペン黒、クレヨン(黒)で線引きし、次の方法で汚
染防止能を観察した。
A line was drawn with a black oil pen and a crayon (black), and the stain prevention ability was observed using the following method.

a)線引き直後に乾いたガーゼでふく(30回、以下同
様) b)線引き30分後、消しゴムで消す。
a) Immediately after drawing, wipe with dry gauze (30 times, same applies below) b) After 30 minutes of drawing, erase with an eraser.

C)線引き30分後、乾いたガーゼでふくd)線引き3
0分後、水でぬれたガーゼでふくe)線引き30分後、
エタノールでぬれたガーゼでふくf)線引き30分後、
石鹸水(pHIO)でぬれたカーゼてふく判定、00 
汚れ完全に除去。
C) Wipe with dry gauze after 30 minutes of drawing d) Drawing 3
After 0 minutes, wipe with water-soaked gauze e) After 30 minutes of drawing,
Wipe with gauze moistened with ethanol f) After 30 minutes of drawing,
Curse cloth wet with soapy water (pHIO) judgment, 00
Completely removes dirt.

0 、僅かに残る × ・かなり残る ××、大部仕残る 結果は第4表のとおりてあった。0, slightly remaining × ・Remains quite a bit XX, Obe remains The results are shown in Table 4.

第4表 10  中和品の水分散性; S−1,5−2□5−3.  S−比−1の各溶液を、
結合カルボン酸と当量のモノエタノールアミンを加えて
中和し、微黄色殆ど透明の溶液を得た。これをPETフ
ィルムに上記同様塗布乾燥し、水を滴下した。′いずれ
も数分後、皮膜は膨潤剥離し、拭うと完全に除去された
Table 4 10 Water dispersibility of neutralized product; S-1,5-2□5-3. Each solution of S-ratio-1,
Neutralization was achieved by adding an amount of monoethanolamine equivalent to the bound carboxylic acid to obtain a slightly yellow, almost clear solution. This was coated on a PET film in the same manner as above, dried, and water was added dropwise. 'After several minutes, the film swelled and peeled off, and was completely removed by wiping.

Claims (1)

【特許請求の範囲】 1、(A)一般式 ▲数式、化学式、表等があります▼ [式中、Xはラジカル重合性基、R^1は炭素数1〜2
0の1価炭化水素基、1価ハロゲン化炭化水素基または
式▲数式、化学式、表等があります▼(式中、R^2は
炭素数1〜20の1価炭化水素基または1価ハロゲン化
炭化水素基の1種または2種以上の基、pは5〜100
の整数である)で示される基から選ばれる1種または2
種以上の基、ただし、一般式中のすべてのR^1のうち
式▲数式、化学式、表等があります▼で示される基は0
、1または2個、mは1〜10の整数、nは5〜100
の整数である]で示される化合物10〜60重量% (B)アクリル酸エステルまたはメタクリル酸エステル
25〜75重量% および (C)カルボキシル基含有モノエチレン性不飽和単量体
5〜20重量% (ただし、(A)+(B)+(C)=100重量%)を
ラジカル重合開始剤の存在下に重合させて得られるシリ
コーン/アクリル共重合体を主成分とする組成物。 2、シリコーン/アクリル共重合体をアルコールに溶解
させてなる請求項1記載の組成物。
[Claims] 1. (A) General formula ▲ Numerical formula, chemical formula, table, etc. ▼ [In the formula, X is a radically polymerizable group, and R^1 has 1 to 2 carbon atoms.
0 monovalent hydrocarbon group, monovalent halogenated hydrocarbon group or formula ▲ Numerical formula, chemical formula, table, etc. ▼ (In the formula, R^2 is a monovalent hydrocarbon group having 1 to 20 carbon atoms or monovalent halogen One or more types of carbonized hydrocarbon groups, p is 5 to 100
1 or 2 selected from the groups represented by
Groups of more than one species, however, among all R^1 in the general formula, groups represented by the formula ▲There are mathematical formulas, chemical formulas, tables, etc.▼ are 0
, 1 or 2, m is an integer of 1 to 10, n is 5 to 100
is an integer of 10 to 60% by weight (B) 25 to 75% by weight of an acrylic ester or methacrylic ester and (C) 5 to 20% by weight of a carboxyl group-containing monoethylenically unsaturated monomer ( However, a composition whose main component is a silicone/acrylic copolymer obtained by polymerizing (A) + (B) + (C) = 100% by weight) in the presence of a radical polymerization initiator. 2. The composition according to claim 1, wherein the silicone/acrylic copolymer is dissolved in alcohol.
JP63151551A 1988-06-20 1988-06-20 Silicone / acrylic copolymer composition Expired - Lifetime JP2638612B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63151551A JP2638612B2 (en) 1988-06-20 1988-06-20 Silicone / acrylic copolymer composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63151551A JP2638612B2 (en) 1988-06-20 1988-06-20 Silicone / acrylic copolymer composition

Publications (2)

Publication Number Publication Date
JPH01319518A true JPH01319518A (en) 1989-12-25
JP2638612B2 JP2638612B2 (en) 1997-08-06

Family

ID=15520995

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63151551A Expired - Lifetime JP2638612B2 (en) 1988-06-20 1988-06-20 Silicone / acrylic copolymer composition

Country Status (1)

Country Link
JP (1) JP2638612B2 (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6013754A (en) * 1998-01-16 2000-01-11 Courtaulds Coatings, Inc. Heavy Duty Division Catalyst free primer coating compositions
JP2000103931A (en) * 1998-09-30 2000-04-11 Dow Corning Toray Silicone Co Ltd Thermoplastic resin composition
US6306992B1 (en) 1999-07-30 2001-10-23 Dow Corning Toray Silicone Company, Ltd. Carbosiloxane dendrimer and dendrimer-containing organic polymers
US6420504B1 (en) 1997-06-12 2002-07-16 Dow Corning Toray Silicone Co., Ltd. Branched siloxane/silalkylene copolymer, silicone-containing organic polymer, and process for producing the same
JP2011057963A (en) * 2009-08-12 2011-03-24 Chisso Corp Surface treating agent
EP2602279A1 (en) 2011-12-07 2013-06-12 Shin-Etsu Chemical Co., Ltd. Silicone-modified wax, composition and cosmetic preparation containing the same, and production method of silicone-modified wax
JP2014125559A (en) * 2012-12-26 2014-07-07 Henkel Japan Ltd Composition for floor polish
WO2019003898A1 (en) * 2017-06-28 2019-01-03 東レ・ダウコーニング株式会社 Film-forming agent for cosmetics and cosmetics containing same
WO2020017535A1 (en) 2018-07-17 2020-01-23 富士フイルム株式会社 Composition for layering material used in medical lubricating member, layering material used in medical lubricating member, medical lubricating member, medical instrument, and production method for layering material used in medical lubricating member.
WO2020142474A1 (en) * 2018-12-31 2020-07-09 Dow Silicones Corporation Acrylate-functional branched organosilicon compound, method of preparing same, and copolymer formed therewith
US11180595B2 (en) 2017-06-28 2021-11-23 Dow Toray Co., Ltd. Copolymer having carbosiloxane dendrimer structure and acidic group, composition containing same, and cosmetic
US11820846B2 (en) 2018-12-31 2023-11-21 Dow Silicones Corporation Composition, method of preparing copolymer, and methods and end uses thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS496548A (en) * 1972-05-10 1974-01-21
JPS60219207A (en) * 1984-04-14 1985-11-01 Chisso Corp Thermosetting acrylic resin composition for coating metallic material
JPS6119606A (en) * 1984-07-05 1986-01-28 Toagosei Chem Ind Co Ltd Production of actinic energy ray-curable silicone graft polymer
JPS6257121A (en) * 1985-09-05 1987-03-12 Toagosei Chem Ind Co Ltd Magnetic recording medium
JPS62156172A (en) * 1985-12-27 1987-07-11 Nippon Oil & Fats Co Ltd Underwater antifouling coating agent

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS496548A (en) * 1972-05-10 1974-01-21
JPS60219207A (en) * 1984-04-14 1985-11-01 Chisso Corp Thermosetting acrylic resin composition for coating metallic material
JPS6119606A (en) * 1984-07-05 1986-01-28 Toagosei Chem Ind Co Ltd Production of actinic energy ray-curable silicone graft polymer
JPS6257121A (en) * 1985-09-05 1987-03-12 Toagosei Chem Ind Co Ltd Magnetic recording medium
JPS62156172A (en) * 1985-12-27 1987-07-11 Nippon Oil & Fats Co Ltd Underwater antifouling coating agent

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6420504B1 (en) 1997-06-12 2002-07-16 Dow Corning Toray Silicone Co., Ltd. Branched siloxane/silalkylene copolymer, silicone-containing organic polymer, and process for producing the same
US6013754A (en) * 1998-01-16 2000-01-11 Courtaulds Coatings, Inc. Heavy Duty Division Catalyst free primer coating compositions
JP2000103931A (en) * 1998-09-30 2000-04-11 Dow Corning Toray Silicone Co Ltd Thermoplastic resin composition
US6306992B1 (en) 1999-07-30 2001-10-23 Dow Corning Toray Silicone Company, Ltd. Carbosiloxane dendrimer and dendrimer-containing organic polymers
JP2011057963A (en) * 2009-08-12 2011-03-24 Chisso Corp Surface treating agent
EP2602279A1 (en) 2011-12-07 2013-06-12 Shin-Etsu Chemical Co., Ltd. Silicone-modified wax, composition and cosmetic preparation containing the same, and production method of silicone-modified wax
JP2014125559A (en) * 2012-12-26 2014-07-07 Henkel Japan Ltd Composition for floor polish
US11180595B2 (en) 2017-06-28 2021-11-23 Dow Toray Co., Ltd. Copolymer having carbosiloxane dendrimer structure and acidic group, composition containing same, and cosmetic
WO2019003898A1 (en) * 2017-06-28 2019-01-03 東レ・ダウコーニング株式会社 Film-forming agent for cosmetics and cosmetics containing same
CN110996900A (en) * 2017-06-28 2020-04-10 陶氏东丽株式会社 Skin film forming agent for cosmetic and cosmetic containing same
JPWO2019003898A1 (en) * 2017-06-28 2020-04-30 ダウ・東レ株式会社 Film-forming agent for cosmetics, and cosmetics containing the same
WO2020017535A1 (en) 2018-07-17 2020-01-23 富士フイルム株式会社 Composition for layering material used in medical lubricating member, layering material used in medical lubricating member, medical lubricating member, medical instrument, and production method for layering material used in medical lubricating member.
JPWO2020017535A1 (en) * 2018-07-17 2021-02-18 富士フイルム株式会社 A method for producing a composition for a laminated material used for a medical lubricating member, a laminated material used for a medical lubricating member, a medical lubricating member, and a medical device, and a laminated material used for a medical lubricating member.
US11845247B2 (en) 2018-07-17 2023-12-19 Fujifilm Corporation Composition for laminated material used for medical lubricating member, laminated material used for medical lubricating member, medical lubricating member, medical device, and method for producing laminated material used for medical lubricating member
CN113330055A (en) * 2018-12-31 2021-08-31 美国陶氏有机硅公司 Acrylate-functional branched organosilicon compounds, methods of making, and copolymers formed therewith
WO2020142474A1 (en) * 2018-12-31 2020-07-09 Dow Silicones Corporation Acrylate-functional branched organosilicon compound, method of preparing same, and copolymer formed therewith
US11820846B2 (en) 2018-12-31 2023-11-21 Dow Silicones Corporation Composition, method of preparing copolymer, and methods and end uses thereof

Also Published As

Publication number Publication date
JP2638612B2 (en) 1997-08-06

Similar Documents

Publication Publication Date Title
US5716603A (en) Aqueous nail polish compositions containing acrylic resins crosslinked with acrylated urethane oligomers
EP1230314B1 (en) Release coating formulation providing low adhesion release surfaces for pressure sensitive adhesives
US5229435A (en) Skin-protecting composition
JP2638612B2 (en) Silicone / acrylic copolymer composition
JP2002241698A (en) Smoothing agent for coating and ink
JP2895589B2 (en) Water based nail polish
JPS6033858B2 (en) Coating composition
JP4684465B2 (en) Organopolysiloxane thioblock vinyl copolymer and antifouling coating composition containing the copolymer
JP2856932B2 (en) Coating composition
JP3713573B2 (en) Easy-to-removable plastic material for daily pollutants
JP2766300B2 (en) (Meth) acrylate copolymer
US3699067A (en) Acrylic terpolymer resins plasticized with silicone oils
JP2683063B2 (en) Resin composition for plastic coating
JP2001206918A5 (en)
JPS5837060A (en) Water-based coating composition
JP3395450B2 (en) Binder resin for primer for hydraulic transfer sheet
JP2920661B2 (en) Nail polish
JPH0623263B2 (en) Vinyl chloride resin molded product
JPS6150510B2 (en)
JP2001207004A5 (en)
JP3801763B2 (en) Water-based ink composition
JP2841621B2 (en) Heat-curable antifogging agent composition for plastic molding material and plastic molding material coated with antifogging cosmetic film
JP2004059812A (en) Coating agent composition
JPH05213719A (en) Manicure
JP4572723B2 (en) Coating composition for polyolefin resin