JPS58217578A - Antifogging agent - Google Patents

Antifogging agent

Info

Publication number
JPS58217578A
JPS58217578A JP57098484A JP9848482A JPS58217578A JP S58217578 A JPS58217578 A JP S58217578A JP 57098484 A JP57098484 A JP 57098484A JP 9848482 A JP9848482 A JP 9848482A JP S58217578 A JPS58217578 A JP S58217578A
Authority
JP
Japan
Prior art keywords
acid
surfactant
copolymer
antifogging
methacrylic
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.)
Pending
Application number
JP57098484A
Other languages
Japanese (ja)
Inventor
Yasuo Ozawa
小沢 保雄
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.)
Hoya Corp
Hoya Lens Corp
Original Assignee
Hoya Corp
Hoya Lens Corp
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
Application filed by Hoya Corp, Hoya Lens Corp filed Critical Hoya Corp
Priority to JP57098484A priority Critical patent/JPS58217578A/en
Priority to SE8303260A priority patent/SE8303260L/en
Priority to DE19833320934 priority patent/DE3320934A1/en
Publication of JPS58217578A publication Critical patent/JPS58217578A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10Optical coatings produced by application to, or surface treatment of, optical elements
    • G02B1/18Coatings for keeping optical surfaces clean, e.g. hydrophobic or photo-catalytic films
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/18Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10Optical coatings produced by application to, or surface treatment of, optical elements
    • GPHYSICS
    • G02OPTICS
    • G02CSPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
    • G02C11/00Non-optical adjuncts; Attachment thereof
    • G02C11/08Anti-misting means, e.g. ventilating, heating; Wipers

Abstract

PURPOSE:To provide an antifogging agent having an excellent and durable antifogging effect, prepared by the combined use of a polymethacrylic acid or methacrylic acid/acrylic acid copolymer and a surfactant. CONSTITUTION:The antifogging agent consists of a polymethacrylic acid or a copolymer of methacrylic and acrylic acids and contains water and/or alcohol as solvent. The polymethacrylic acid and the methacrylic acid/acrylic acid copolymer has a degree of polymerization of 500-10,000, pref. 1,000-3,000. When it exceeds 10,000, the antifogging effect is lessened. The surfactant should pref. have excellent detergent action and hygroscopicity and it includes sodium dodecylbenzenesulfonate and polyoxyethylene alkyl ether.

Description

【発明の詳細な説明】 本発明は、ガラスなどの透明物質表面の斡り防止剤に関
し、その目的とするところは、防曇効果に優れ、その効
力持続性が大きく且つ透明均一な被膜を透明物質表面に
与え得る曇り防止剤を提供するにある′。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an anti-fogging agent for the surface of transparent materials such as glass, and its purpose is to have an excellent anti-fogging effect, long-lasting effect, and to form a transparent and uniform coating. The object of the present invention is to provide an anti-fogging agent that can be applied to the surface of a material.

寒い所から暖かい部屋に入った時、眼鏡が畝ったり、寒
い朝のひけそり時蒸しタオルの湯気で錬が曇ったりする
ことは、日常しばしば見られる現象である。とのような
微細な水滴の付着による曇りは、時に非常な不便を感じ
させるばかりでなく、ある場合には危険にもつながる。
It is a common phenomenon in everyday life for glasses to become ridged when you enter a warm room from a cold place, or for glasses to fog up due to the steam from a steaming towel on a cold morning. Clouding caused by the adhesion of minute water droplets not only causes great inconvenience, but can also be dangerous in some cases.

このような水滴の付着による艙りを防止するために、ガ
ラスなどの表面に塗布して用いるソーダ石けん、ツブレ
スソープ、ロート油、硫酸ニス゛チル塩、脂肪酸エステ
ル、ポリエチレングリコール、などの湿潤性のある界面
活性剤を主剤とした曇り防止剤が考えられ、且つ市販さ
れている。これらの曇り防止剤は、ガラス表面に凝縮付
着する水分の表面張力を小さくして水分が水滴の状態に
届らず、一様に広がった薄膜となって、表面をぬらすよ
うにして、防曇効果を奏するものである。
In order to prevent water droplets from sticking to the surface, wetting agents such as soda soap, soap, funnel oil, nitrous sulfate, fatty acid esters, polyethylene glycol, etc., are used to coat the surface of glass, etc. Anti-fogging agents based on surfactants have been considered and are commercially available. These anti-fog agents reduce the surface tension of the water that condenses on the glass surface so that the water does not reach the state of water droplets and forms a uniformly spread thin film that wets the surface. It is effective.

しかしながら、これらの曇り防止剤は界面活性剤を主剤
とする関係上いずれも凝縮水分によって、流れ落ちやす
く、効力持続性に乏しい欠点を持っている。
However, since these anti-fogging agents are mainly composed of surfactants, they tend to run off due to condensed water, and have the disadvantage of having poor long-lasting efficacy.

妊り防止剤が具備すべき好ましい性質は、ガラスなどの
透明物質表面透明均一な被膜を形成すること、そしで、
その形成被膜が防曇性能に榎れていると同時に、透明物
質表面との密着性が良く長時間脱離しない強固なもので
あることである。
Preferable properties that the anti-fertility agent should have include forming a transparent uniform film on the surface of a transparent substance such as glass, and
The formed film has excellent antifogging performance, and at the same time, it has good adhesion to the surface of the transparent material and is strong enough to not come off for a long time.

このような性質を具備する絃り防止剤を指向し提案は既
に幾つかなされているが、満足すべき状態のものはない
Several proposals have already been made towards anti-friction agents having such properties, but none are in a satisfactory state.

本発明者は、以上に鑑み鋭意研究の結果、ポリメタクリ
酸あるいはメタクリル酸とアクリル酸の共重合体を界面
活性剤と併用することにより、防曇性能と持続性に優れ
た曇り防止剤が得られることを見出し本発明に到達した
のである。
In view of the above, as a result of intensive research, the present inventors have found that by using polymethacrylic acid or a copolymer of methacrylic acid and acrylic acid in combination with a surfactant, an antifogging agent with excellent antifogging performance and durability can be obtained. They discovered this and arrived at the present invention.

すなわち、本発明の曇り防止組成物は、ポリメタクリル
酸あるいはメタクリル酸とアクリル酸の共ル合体及び界
面活剤を含有し、溶媒として水又は/及びアルコールを
用いてなる組成物である。
That is, the anti-fogging composition of the present invention is a composition containing polymethacrylic acid or a combination of methacrylic acid and acrylic acid and a surfactant, and using water and/or alcohol as a solvent.

本発明のポリメタクリル酸、メタクリル酸とアクリル酸
の共重合体としては重合度500〜10000のものが
用いうるが、特に1000〜30000重合度のものが
好ましい。重合度500未満のものは、水により流れ落
ちやすく、持続性の点で不十分であり重合度10.00
0より大きくなると、防曇性能を減少をもたらす。なお
、メタクリル酸とアクリル酸の共重合比はメタクリル酸
100〜20チにアクリル酸O〜80%の範囲が公的に
用いうる。
As the polymethacrylic acid and the copolymer of methacrylic acid and acrylic acid of the present invention, those having a degree of polymerization of 500 to 10,000 can be used, but those having a degree of polymerization of 1,000 to 30,000 are particularly preferred. If the degree of polymerization is less than 500, it will easily wash off with water and will be insufficient in terms of sustainability.
When it becomes larger than 0, the anti-fog performance decreases. Incidentally, the copolymerization ratio of methacrylic acid and acrylic acid may be in the range of 100% to 20% methacrylic acid and 0% to 80% acrylic acid.

本発明に用いられる界面活性剤としては、水とポリメタ
クリル酸及びメタクリル酸とアクリル酸の共重合体に親
和性のあるyr−面活性剤・はすべて用い得る。中でも
洗沙及び吸湿性に優れたものが特に好ましく例示として
、ドデシルベンゼンスルホン酸ナトリウム、ボ”リオキ
/エグーレンアルキルエー チル、;K ’) オキ/
エチレンアルキルフェニルエーテルなどがあげられる。
As the surfactant used in the present invention, any yr-surfactant having an affinity for water and polymethacrylic acid and a copolymer of methacrylic acid and acrylic acid can be used. Among them, those with excellent detergency and moisture absorption are particularly preferred, such as sodium dodecylbenzene sulfonate, borioki/egulene alkyl ethyl, ;K') oxy/
Examples include ethylene alkylphenyl ether.

本発明の!表り防止剤の各成分組成は広い範囲に渡って
有効であるが、透明均一で、vノ曇効果が擾れ且つ、効
力持続性が良好な範囲はポリメタクリル酸あるいはメタ
クリル酸とアクリル酸の共1合体を0.1〜101%、
界面活性剤10〜50ル箪チ、溶媒としての水又は/及
びアルコール60〜90ル箪チの範囲である。
The invention! The composition of each component of the anti-surface agent is effective over a wide range, but the range in which it is transparent, uniform, has no clouding effect, and has a good long-lasting effect is polymethacrylic acid or methacrylic acid and acrylic acid. 0.1 to 101% of co-1 coalescence,
The surfactant ranges from 10 to 50 kg, water and/or alcohol as a solvent ranges from 60 to 90 kg.

また、本発明の仏り防止剤に、殺菌力、防錆力を付与す
る目的でイミダプリン系両性界面活性剤例えばリポミン
OOH(ライオン油脂社製)を少量添加したり、個れを
良くする目的でンリコーンブロツクコボ゛リマーである
L70(Jl、L720、L7600.Y2O,06(
いずれも信越化学社製)ヤ非イオン界面活性剤のポリオ
キシアルキルフェニルエーテル例えばりボノツクスNC
I (ライオン油脂社製)などを少量添加しうろことは
もちろんである。
In addition, a small amount of an imidapurine-based amphoteric surfactant such as Lipomin OOH (manufactured by Lion Oil Co., Ltd.) may be added to the anti-foaming agent of the present invention for the purpose of imparting bactericidal and anticorrosion properties, or for the purpose of improving the flaking properties. L70 (Jl, L720, L7600.Y2O,06(
Both are manufactured by Shin-Etsu Chemical Co., Ltd.) Polyoxyalkyl phenyl ethers of nonionic surfactants such as Bonox NC
Of course, scales can be added with a small amount of I (manufactured by Lion Oil Co., Ltd.).

本発明の防曇剤は従来技術に比して、防も性の持続性に
おいて著しい効果が見い出されたものである。
The antifogging agent of the present invention has been found to be significantly more effective in maintaining antifogging properties than those of the prior art.

以下に本発明の実施例を示す。Examples of the present invention are shown below.

実施例1 ポリメタクリル酸(重合度2000) 4.0ル量チ アルキルベンゼンスルホン酸ナトリウム15.0矩量係 純水             81.Oル量チ上記成
分からなる防錠剤をガラス及びプラスチックレンズに塗
布し、−4℃恒温室で30分冷却後、室温20°C1湿
度60%の部屋に取り出し、くもりの発生を調べた。こ
れをくり返し行ったが10回のテストにおいてもくもり
を生じな刀・つた。
Example 1 Polymethacrylic acid (degree of polymerization 2000) 4.0 l quantity Sodium thialkylbenzenesulfonate 15.0 square quantity Pure water 81. A tablet preventive made of the above ingredients was applied to glass and plastic lenses, cooled for 30 minutes in a constant temperature room at -4°C, and then taken out to a room at a room temperature of 20°C and 60% humidity to examine the occurrence of clouding. I repeated this process, but after 10 tests, no clouding occurred.

実施例2 メタクリル酸とアクリル酸の共m+会合体M3成比40
:60、油含IJi3000 )6.0重−φ係 アルキルベンゼンスルホン酸ナトリウム(ライメンif
l+ ljxライボンF )    15.0沖量係純
水             82.0重量%実施例1
と同様のテストにおいて、くり返し10回でもくもりを
生じなかった。
Example 2 Co-m+aggregate M3 composition ratio of methacrylic acid and acrylic acid 40
: 60, oil-containing IJi3000) 6.0 weight-φ related sodium alkylbenzenesulfonate (Limen if
l+ ljx Libon F) 15.0 offshore weight pure water 82.0% by weight Example 1
In a similar test, no clouding occurred even after 10 repetitions.

)(lイu’す6 ポリメタクリル酸(重合度11JOO)1.0油量チ アルキルベンゼンスルホン酸ナトリウム(ライオン重重
hライフ1ぞンF )    14.0重量予エチルア
ルコール       85.Oルミ%実施例1と狗様
のテストにおいて、くり返し10でもくもりを生じなか
った。
) (l u'su 6 Polymethacrylic acid (degree of polymerization 11 JOO) 1.0 oil amount Sodium thialkylbenzenesulfonate (Lion Heavy Life 1 Zone F) 14.0 weight Pre-ethyl alcohol 85.0 Lumi% Example In the tests of 1 and 10, no clouding occurred even after repeated tests of 10.

実施例4 ポリメタクリル酸(重合度2L]00)4.Om藁チア
ルキルベンゼンスルホン酸ナトリウム(ライオン油脂ラ
イポンF)   14.0重t%純水        
     72,0重量%エチルアルコール     
  10.0重量%実施例1と同様のテストにおいて、
くり返し10回のテストで、くもりを生じなかった。
Example 4 Polymethacrylic acid (degree of polymerization 2L] 00) 4. Om Straw Sodium Thialkylbenzenesulfonate (Lion Oil Lypon F) 14.0 wt% Pure water
72.0% by weight ethyl alcohol
10.0% by weight In a test similar to Example 1,
After 10 repeated tests, no clouding occurred.

比較例1 ポリアクリル酸(重合度500)  0.5庫量チアル
キルベンゼンスルホン酸ナトリウム(ライオン油脂ライ
ボンF )   14.5 m’:if%純水    
         85.0軍量%実施例1と同様のテ
ストで、防セ性は、実施例1〜4と同程度であるが、く
り返しテスト4回目から一部くもりを生じてしfつだ。
Comparative Example 1 Polyacrylic acid (degree of polymerization 500) 0.5 storage amount Sodium thialkylbenzenesulfonate (Lion Oil Libon F) 14.5 m': if% pure water
85.0 Military % In a test similar to Example 1, the anti-seizure properties were comparable to Examples 1 to 4, but some clouding began to occur from the fourth repeated test.

代理人 浅 村   皓 外4名Agent Asamura Hao 4 other people

Claims (1)

【特許請求の範囲】[Claims] ポリメタクリル酸あるいはメタクリル酸とアクリル酸の
共重合体及び界面活性剤を含有し、水又は/及びアルコ
ールを溶剤として用いる曇り防止剤。
An anti-fogging agent containing polymethacrylic acid or a copolymer of methacrylic acid and acrylic acid and a surfactant, and using water and/or alcohol as a solvent.
JP57098484A 1982-06-10 1982-06-10 Antifogging agent Pending JPS58217578A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP57098484A JPS58217578A (en) 1982-06-10 1982-06-10 Antifogging agent
SE8303260A SE8303260L (en) 1982-06-10 1983-06-09 IMAGING DISABILITIES
DE19833320934 DE3320934A1 (en) 1982-06-10 1983-06-09 Antifogging agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57098484A JPS58217578A (en) 1982-06-10 1982-06-10 Antifogging agent

Publications (1)

Publication Number Publication Date
JPS58217578A true JPS58217578A (en) 1983-12-17

Family

ID=14220919

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57098484A Pending JPS58217578A (en) 1982-06-10 1982-06-10 Antifogging agent

Country Status (3)

Country Link
JP (1) JPS58217578A (en)
DE (1) DE3320934A1 (en)
SE (1) SE8303260L (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02148017A (en) * 1988-11-30 1990-06-06 Taiho Ind Co Ltd Method, material and means for defogging of spectacles
JP2002363546A (en) * 2001-06-01 2002-12-18 Fumakilla Ltd Anti-fogging agent and method for treatment therewith
JP2011179007A (en) * 2011-04-18 2011-09-15 Fumakilla Ltd Anti-fogging agent and treatment method therewith
CN102516943A (en) * 2011-12-08 2012-06-27 华北电力大学 Complex liquid for preventing fog on spectacle glasses
CN103694957A (en) * 2012-09-28 2014-04-02 中国石油化工股份有限公司 Glass antifogging agent and preparation method thereof
CN103694958A (en) * 2012-09-28 2014-04-02 中国石油化工股份有限公司 Glass antifogging agent and preparation method thereof
CN104086088A (en) * 2014-06-07 2014-10-08 北京化工大学 Method of preparing glass with surface antibacterial property by photopolymerization
CN113105868A (en) * 2021-04-19 2021-07-13 江苏南创化学与生命健康研究院有限公司 Antibacterial antifogging agent and antibacterial long-acting antifogging wet tissue prepared from same

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02148017A (en) * 1988-11-30 1990-06-06 Taiho Ind Co Ltd Method, material and means for defogging of spectacles
JP2002363546A (en) * 2001-06-01 2002-12-18 Fumakilla Ltd Anti-fogging agent and method for treatment therewith
JP2011179007A (en) * 2011-04-18 2011-09-15 Fumakilla Ltd Anti-fogging agent and treatment method therewith
CN102516943A (en) * 2011-12-08 2012-06-27 华北电力大学 Complex liquid for preventing fog on spectacle glasses
CN103694957A (en) * 2012-09-28 2014-04-02 中国石油化工股份有限公司 Glass antifogging agent and preparation method thereof
CN103694958A (en) * 2012-09-28 2014-04-02 中国石油化工股份有限公司 Glass antifogging agent and preparation method thereof
CN104086088A (en) * 2014-06-07 2014-10-08 北京化工大学 Method of preparing glass with surface antibacterial property by photopolymerization
CN113105868A (en) * 2021-04-19 2021-07-13 江苏南创化学与生命健康研究院有限公司 Antibacterial antifogging agent and antibacterial long-acting antifogging wet tissue prepared from same
CN113105868B (en) * 2021-04-19 2022-05-17 江苏南创化学与生命健康研究院有限公司 Antibacterial antifogging agent and antibacterial long-acting antifogging wet tissue prepared from same

Also Published As

Publication number Publication date
DE3320934A1 (en) 1983-12-15
SE8303260D0 (en) 1983-06-09
SE8303260L (en) 1983-12-11

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