JPS6123960B2 - - Google Patents
Info
- Publication number
- JPS6123960B2 JPS6123960B2 JP57002592A JP259282A JPS6123960B2 JP S6123960 B2 JPS6123960 B2 JP S6123960B2 JP 57002592 A JP57002592 A JP 57002592A JP 259282 A JP259282 A JP 259282A JP S6123960 B2 JPS6123960 B2 JP S6123960B2
- Authority
- JP
- Japan
- Prior art keywords
- protective coating
- cleaning
- weight
- cleaning agent
- present
- 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
- 239000011253 protective coating Substances 0.000 claims description 10
- 150000008282 halocarbons Chemical class 0.000 claims description 8
- 239000012459 cleaning agent Substances 0.000 claims description 7
- 230000002209 hydrophobic effect Effects 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- 238000006386 neutralization reaction Methods 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- 238000004140 cleaning Methods 0.000 description 9
- -1 methylene chloride Chemical class 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 1
- ZXUJWPHOPHHZLR-UHFFFAOYSA-N 1,1,1-trichloro-2-fluoroethane Chemical compound FCC(Cl)(Cl)Cl ZXUJWPHOPHHZLR-UHFFFAOYSA-N 0.000 description 1
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 1
- PIPCWAOGKLETLY-UHFFFAOYSA-N C(CCCCCCCCCCC)N.C(=C)=O Chemical compound C(CCCCCCCCCCC)N.C(=C)=O PIPCWAOGKLETLY-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229940017219 methyl propionate Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004971 nitroalkyl group Chemical group 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- WRKCIHRWQZQBOL-UHFFFAOYSA-N octyl dihydrogen phosphate Chemical compound CCCCCCCCOP(O)(O)=O WRKCIHRWQZQBOL-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Description
本発明は保護塗膜洗浄剤に関するものであり、
特にはレンズの表面に設けられている保護塗膜を
容易にしかも完全に除去することができる洗浄剤
の提供を目的とする。
光学用レンズ等のレンズはその加工時に貼着し
たりまたはそれをはがし取つたりする操作が行わ
れるが、その際レンズ表面にキズがつくのを回避
するために、通常レンズ表面に保護塗膜を設ける
ことが行われており、この保護塗膜としては主に
塩化ビニル樹脂塗料、ブチラール樹脂塗料等の合
成樹脂塗料やパラフインワツクス等が使用されて
いる。
加工等の作業終了後は上記保護塗膜を洗浄除去
する必要があり、従来このための洗浄剤として
は、塩化メチレン、トリクロルトリフルオロエタ
ン、1,1,1−トリクロルエタン、トリクロル
エチレン、テトラクロルエチレン等のハロゲン化
炭化水素類の使用が試みられている。これらのう
ちでも特に塩化メチレンは強力な溶解力、低毒
性、不燃性に加えて化学的にかなり安定性が高い
という特長をもつているのであるが、こうしたハ
ロゲン化炭化水素単独では期待する洗浄効果(保
護塗膜の容易かつ完全な除去)を達成することが
困難であるという問題点がある。従来これを解決
するためにある種の添加剤を加える試みが種々行
われているが、十分に満足すべき結果は得られて
いない。
本発明者らは上記した点にかんがみ、ハロゲン
化炭化水素特に塩化メチレンが本来有する性能・
特長を阻害することなく、これに他の物質を比較
的少量添加することで、よりすぐれた洗浄効果を
達成することを目的として鋭意研究を重ねた結
果、ハロゲン化炭化水素に疎水性界面活性剤を添
加することにより、上記目的が満足されることを
見出し、本発明を完成した。
以下本発明を詳細に説明する。
本発明に使用される主剤としてのハロゲン化炭
化水素には、塩化メチレン、トリクロルフルオロ
エタン、1,1,1−トリクロルエタン、トリク
ロルエチレン、テトラクロルエチレン等が包含さ
れるが、これらのうちでも塩化メチレンが特に望
ましい。
上記ハロゲン化炭化水素に添加使用される疎水
性界面活性剤としては、モノまたはジオキシエチ
レンパルミチルアミン、モノまたはジオキシエチ
レンラウリルアミン、モノまたはジオキシプロピ
レンラウリルアミン等のモノまたはポリオキシア
ルキレンアルキルアミン、モノまたはジオクチル
りん酸エステル/2−エチルヘキシルアミン中和
物、モノオキシエチレンラウリルエチルアミン/
カプリル酸中和物、モノオキシエチレンラウリル
アミン/2−エチルヘキシル酸中和物等の飽和脂
肪族アミンと有機酸との中和生成物が例示され
る。
また、本発明ではぎ酸エチル、酢酸メチル、酢
酸エチル、酢酸n−ブチル、プロピオン酸メチ
ル、酪酸エチル等のモノカルボン酸エステルを疎
水性界面活性剤に添加することにより、すぐれた
効果を得ることができる。
ハロゲン化炭化水素に対する上記添加剤の配合
割合は、疎水性界面活性剤の場合0.01〜10重量%
(好ましくは0.1〜5重量%)の範囲、モノカルボ
ン酸エステルの場合1〜50重量%(好ましくは10
〜30重量%)の範囲とすることが必要とされ、そ
れら添加成分の添加量が少なすぎると十分な洗浄
効果が得られず、他方上記したそれぞれの範囲を
越える多量を加えても、それ以上の効果が得られ
ないのみならず、経済的に不利でかつ可燃性にな
る。
なお、このようにして得られる保護塗膜洗浄剤
には必要に応じ安定剤を添加することが望まし
く、この安定剤としてはプロピレンオキシド、ブ
チレンオキシド等のエポキシド類、ジイソプロピ
ルアミン、イソプロピルアミン等のアミン類、ニ
トロメタン、ニトロエタン等のニトロアルカン
類、メタノール、エタノール等のアルコール類が
例示される。
本発明の洗浄剤を用いることにより、レンズ表
面に設けられていた保護塗膜(合成樹脂塗料やパ
ラフインワツクス等)を比較的簡単な洗浄工程で
しかも完全に除去することができ、洗浄コストも
低く経済的であるという利点が与えられる。
つぎに、具体的実施例をあげる。
実施例(実験No.1〜16)
塩化ビニル樹脂保護塗料(白色)を写真用凹凸
レンズ(30mmφ)50枚に塗り、1時間放置した。
この保護塗膜の設けられた50枚のレンズを洗浄カ
ゴに入れ、つぎに洗浄カゴを四槽式超音波洗浄機
に順次入れて洗浄し、仕上がり具合を目視判定し
て合格率を調べた。洗浄時間は各槽1分ずつ、洗
浄剤は第一槽には表中に記載のものを使用し、第
二、三および四槽には安定剤入塩化メチレンを使
用した。結果は表に示すとおりであつた。ただ
し、実験No.1〜6は本発明、No.7〜11は比較例を
示したものである。
The present invention relates to a protective coating film cleaning agent,
In particular, the object is to provide a cleaning agent that can easily and completely remove a protective coating film provided on the surface of a lens. Lenses such as optical lenses are attached and removed during processing, but in order to avoid scratches on the lens surface, a protective coating is usually applied to the lens surface. As this protective coating, synthetic resin coatings such as vinyl chloride resin coatings and butyral resin coatings, paraffin wax, etc. are mainly used. After finishing work such as processing, it is necessary to wash and remove the protective coating film, and conventional cleaning agents for this purpose include methylene chloride, trichlorotrifluoroethane, 1,1,1-trichloroethane, trichloroethylene, and tetrachloride. Attempts have been made to use halogenated hydrocarbons such as ethylene. Among these, methylene chloride in particular has the features of strong dissolving power, low toxicity, non-flammability, and extremely high chemical stability, but these halogenated hydrocarbons alone do not have the expected cleaning effect. (easy and complete removal of the protective coating) is difficult to achieve. In order to solve this problem, various attempts have been made to add certain additives, but no fully satisfactory results have been obtained. In view of the above points, the present inventors have discovered that the inherent performance of halogenated hydrocarbons, particularly methylene chloride,
As a result of extensive research with the aim of achieving better cleaning effects by adding relatively small amounts of other substances without interfering with its properties, we have developed a hydrophobic surfactant for halogenated hydrocarbons. The present invention was completed based on the discovery that the above object can be achieved by adding . The present invention will be explained in detail below. The halogenated hydrocarbon used as the main ingredient in the present invention includes methylene chloride, trichlorofluoroethane, 1,1,1-trichloroethane, trichlorethylene, tetrachlorethylene, etc. Among these, chlorinated hydrocarbon Methylene is particularly preferred. Hydrophobic surfactants added to the above halogenated hydrocarbons include mono- or polyoxyalkylene alkyls such as mono- or dioxyethylene palmitylamine, mono- or dioxyethylene laurylamine, and mono- or dioxypropylene laurylamine. Amine, mono- or dioctyl phosphate ester/2-ethylhexylamine neutralized product, monooxyethylene laurylethylamine/
Examples include neutralized products of saturated aliphatic amines and organic acids, such as neutralized caprylic acid and neutralized monooxyethylene laurylamine/2-ethylhexylic acid. Furthermore, in the present invention, excellent effects can be obtained by adding monocarboxylic acid esters such as ethyl formate, methyl acetate, ethyl acetate, n-butyl acetate, methyl propionate, and ethyl butyrate to the hydrophobic surfactant. I can do it. The blending ratio of the above additives to the halogenated hydrocarbon is 0.01 to 10% by weight in the case of hydrophobic surfactants.
(preferably 0.1 to 5% by weight), in the case of monocarboxylic acid esters 1 to 50% by weight (preferably 10% by weight)
~30% by weight), and if the amount of these additional components added is too small, sufficient cleaning effect will not be obtained. Not only is this effect ineffective, but it is also economically disadvantageous and flammable. In addition, it is desirable to add a stabilizer to the protective coating film cleaning agent obtained in this way, if necessary, and the stabilizer includes epoxides such as propylene oxide and butylene oxide, and amines such as diisopropylamine and isopropylamine. Examples include nitroalkanes such as nitromethane and nitroethane, and alcohols such as methanol and ethanol. By using the cleaning agent of the present invention, the protective coating film (synthetic resin paint, paraffin wax, etc.) on the lens surface can be completely removed with a relatively simple cleaning process, reducing cleaning costs. It has the advantage of being low and economical. Next, specific examples will be given. Examples (Experiment Nos. 1 to 16) A vinyl chloride resin protective paint (white) was applied to 50 photographic concave and convex lenses (30 mmφ) and left for 1 hour.
The 50 lenses with the protective coating were placed in a cleaning basket, and then the cleaning basket was sequentially placed in a four-tank ultrasonic cleaner for cleaning, and the quality of the finish was visually judged to determine the pass rate. The cleaning time was 1 minute for each tank, and the cleaning agent listed in the table was used for the first tank, and methylene chloride containing stabilizer was used for the second, third, and fourth tanks. The results were as shown in the table. However, Experiment Nos. 1 to 6 show the present invention, and Experiments No. 7 to 11 show comparative examples.
【表】【table】
【表】【table】
Claims (1)
有機酸との中和生成物である疎水性界面活性剤を
0.01〜10重量%添加してなるレンズ表面の保護塗
膜洗浄剤。1 A hydrophobic surfactant, which is a neutralization product of a saturated aliphatic amine and an organic acid, is added to a halogenated hydrocarbon.
A protective coating cleaning agent for lens surfaces containing 0.01 to 10% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP259282A JPS58120700A (en) | 1982-01-11 | 1982-01-11 | Protection paint coating detergent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP259282A JPS58120700A (en) | 1982-01-11 | 1982-01-11 | Protection paint coating detergent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58120700A JPS58120700A (en) | 1983-07-18 |
JPS6123960B2 true JPS6123960B2 (en) | 1986-06-09 |
Family
ID=11533647
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP259282A Granted JPS58120700A (en) | 1982-01-11 | 1982-01-11 | Protection paint coating detergent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58120700A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS49130905A (en) * | 1973-04-05 | 1974-12-16 | ||
JPS5538822A (en) * | 1978-09-11 | 1980-03-18 | Masatoshi Shimizu | Agent for releasing coating and adhesive |
-
1982
- 1982-01-11 JP JP259282A patent/JPS58120700A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS49130905A (en) * | 1973-04-05 | 1974-12-16 | ||
JPS5538822A (en) * | 1978-09-11 | 1980-03-18 | Masatoshi Shimizu | Agent for releasing coating and adhesive |
Also Published As
Publication number | Publication date |
---|---|
JPS58120700A (en) | 1983-07-18 |
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