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JPS6311400B2 - - Google Patents
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JPS6311400B2 - - Google Patents

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Publication number
JPS6311400B2
JPS6311400B2 JP58140575A JP14057583A JPS6311400B2 JP S6311400 B2 JPS6311400 B2 JP S6311400B2 JP 58140575 A JP58140575 A JP 58140575A JP 14057583 A JP14057583 A JP 14057583A JP S6311400 B2 JPS6311400 B2 JP S6311400B2
Authority
JP
Japan
Prior art keywords
weight
water
amount
fatty acid
composition
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
Application number
JP58140575A
Other languages
Japanese (ja)
Other versions
JPS6032898A (en
Inventor
Sadaji Misumi
Hisanori Oomori
Hiroshi Sakaida
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.)
Central Glass Co Ltd
Original Assignee
Central Glass 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
Application filed by Central Glass Co Ltd filed Critical Central Glass Co Ltd
Priority to JP14057583A priority Critical patent/JPS6032898A/en
Publication of JPS6032898A publication Critical patent/JPS6032898A/en
Publication of JPS6311400B2 publication Critical patent/JPS6311400B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、機械類その他種々の部品を洗浄する
ための乳濁液組成物に関し、より詳しくは、
1.1.2―トリクロロ―1.2.2―トリフルオロエタン
(以下フロン113と略記する。)と水を油中水型に
乳化せしめるに際し複数の乳化剤(界面活性剤)
を併用した組成物および当該組成物を安定化せし
めた組成物に関する。 フロン113は選択溶解性、速乾性、化学的安定
性に加え、不燃性、低毒性等洗浄剤としての優れ
た性質を有しており、精密機械用洗浄剤として広
く用いられている。しかしながら純粋なフロン
113では水溶性あるいは水分散性の汚れを除去す
ることが困難であり、水または温水洗浄等との組
合せが必要となる。このような場合により好まし
い洗浄方法として、フロン113に水をw/o型に
乳化させ水溶性あるいは水分散性の汚れをも十分
に除去する組成物を使用する方法が知られてい
る。 フロン113に水を乳化せしめた組成物及びかか
る組成物に用いる乳化剤に特徴を有する提案が
種々なされており、例えば特公昭44−8973号公
報、特公昭53−31471号公報などに開示されてい
る。しかしながらこれらの組成物では乳化剤が一
種類または二種類に限定され、他の物質を添加す
る場合の水の乳化量はかなり低下し、さらに温度
の低下によつても水の乳化量は著しく減少する。
また、亜鉛製品や銅製品を腐食するなどの欠点が
ある。 本発明者は、前記の如き問題点に鑑み鋭意研究
を重ねた結果、フロン113に水を乳化せしめるた
めに複数の乳化剤を併用することにより、少量の
乳化剤でもつて多量の水を乳化し得ると共に、水
の乳化量に対する温度依存性の程度をより小さく
することができ、さらに特定の安定剤の添加によ
り亜鉛製品や銅製品に対しても顕著な安定性を示
すことを見い出し、この知見に基づいて本発明を
なすに至つた。 すなわち本発明の第1は、0.25〜50重量%の水
と、少なくとも30重量%の1,1,2―トリクロ
ロ―1,2,2―トリフルオロエタンからなる油
中水型乳濁液において、次の成分: ドデシルベンゼンスルホン酸イソプロピルア
ミン塩0.08〜36重量%と ソルビタン脂肪酸エステル、ポリオキシエチ
レンソルビタン脂肪酸エステルの少なくとも1
種0.02〜9重量%とを含む洗浄用乳濁液組成物
である。 また、本発明の第2は前記組成物に安定剤とし
て: ニトロアルカン類0.01〜0.5重量%とベンゾト
リアゾール類、メルカプトベンゾイミダゾール、
メルカプトベンゾオキサゾールおよびメルカプト
ベンゾチアゾールのうち少なくとも1種0.005〜
0.05重量%とを含む洗浄用乳濁液組成物である。 本発明で用いるソルビタン脂肪酸エステル、ポ
リオキシエチレンソルビタン脂肪酸エステルはそ
れぞれ次式〔〕、〔〕で示される化合物であ
り、式中 は飽和及び不飽和の脂肪族炭化水素類であり、
また()に示されるl,m,nは任意の整数値
を取り得るがいずれもHLB値が6〜14であるも
のが好ましい。 本発明においては、乳化剤としてドデシルベン
ゼンスルホン酸イソプロピルアミン塩およびソル
ビタン誘導体類を併用するものであるが、ドデシ
ルベンゼンスルホン酸イソプロピルアミン塩単独
では最大乳化量は比較的大きいが、安定乳化域が
狭く、ソルビタン誘導体類を併用することで最大
乳化量が拡大すると同時に、最大乳化量にいたる
まですべての領域で安定的に乳化せしむることが
できるものである。また、乳濁助剤として塩基性
含窒素化合物を添加することにより乳化範囲を拡
大することができ、該化合物の添加も好ましいも
のである。ここで用いる塩基性含窒素化合物とし
ては、脂肪族第1、第2及び第3アミン類、脂環
式アミン類、芳香族アミン類、アンモニア等のす
べてが採用可能である。また、この添加量は乳濁
液組成物100gに対して0.00005〜0.0005モルの範
囲が好ましい。 本発明においては水の量は0.25〜50重量%が好
ましく、50重量%を越えると乳濁液は、油中水型
から水中油型となり好ましくない。 また、0.25重量%以下では水溶性あるいは水分
散性の汚れを除去するための用途に供すには実用
的でなく、好ましくない。 また、フロン―113の特性を活かすにはフロン
113の量は30重量%以上が必要であり、ドデシル
ベンゼンスルホン酸イソプロピルアミン塩は水の
実用的な下限値0.25重量%および上限値50重量%
を乳化するに要する量範囲0.05〜12重量%が適用
される。12重量%以上の使用は、水の乳化安定の
面からは特に必要ではないが、これを越えても特
に支障はない。 ソルビタン誘導体類は、ドデシルベンゼンスル
ホン酸イソプロピルアミン塩に対し通常は20〜30
重量%程度が好ましく、添加量としては0.01〜4
重量%の範囲で使用される。 本発明の第2は特に亜鉛製品や銅製品を腐食す
ることなく良好に用いるため、安定剤を添加した
組成物であり、ベンゾトリアゾール類、メルカプ
トベンゾイミダゾール類、メルカプトベンゾオキ
サゾール類およびメルカプトベンゾチアゾール類
のうち少くとも1種とニトロアルカン類との併用
を特徴とするものである。 ベンゾトリアゾール類としてはアルキル置換基
などを有するメチルベンゾトリアゾール、5―ニ
トロベンゾトリアゾールなども採用可能であるが
置換基をもたないベンゾトリアゾール自身が好適
である。 また、メルカプトベンゾイミダゾール類、メル
カプトベンゾオキサゾール類、メルカプトベンゾ
チアゾール類のいずれについても置換基を有する
ものも採用可能であり、また、これらはそれぞれ
単独で用いてもよいし、2種以上を併用してもよ
い。これら安定剤の添加量は乳濁液に対し0.005
〜0.05重量%の範囲が好ましく、0.005重量%以
下では、安定化の効果が十分に発揮されず、ま
た、0.05重量%以上添加しても特にメリツトはな
く、その必要はない。 本発明において用いられるニトロアルカン類と
しては、ニトロメタン、ニトロエタンが好適であ
るが、2―ニトロプロパンなども採用可能であ
り、通常は炭素数1〜3個のニトロアルカン類か
ら選定され、その添加量は乳濁液に対して0.01〜
0.5重量%の範囲が好ましく、0.01重量%以下で
は、その効果が得られず、0.5重量%以上加えて
も特に優れた効果は期待できず添加する必要はな
い。 次に実施例を挙げ本発明を詳細に説明する。 実施例1〜6、比較例1,2 ドデシルベンゼンスルホン酸イソプロピルアミ
ン塩(DBS―塩)、ソルビタン誘導体類として
ソルビタンモノラウレート、ポリオキシエチレ
ンソルビタンオレエートをフロン113 100重量
部に対し、種々の量添加し、さらに、該組成物
100重量部に対し0.01重量部の塩基性含窒素化合
物を添加して水の安定乳化域を10℃、25℃、35℃
で測定した。この結果を第1表に示す。
The present invention relates to an emulsion composition for cleaning machinery and other various parts, and more specifically,
1.1.2-Trichloro-1.2.2-Trifluoroethane (hereinafter abbreviated as Freon 113) and water are used to emulsify water-in-oil type using multiple emulsifiers (surfactants).
The present invention relates to a composition in which the present invention is used in combination with the present invention, and a composition in which the composition is stabilized. Freon 113 has excellent properties as a cleaning agent, such as selective solubility, quick drying properties, and chemical stability, as well as nonflammability and low toxicity, and is widely used as a cleaning agent for precision machinery. However, pure Freon
113, it is difficult to remove water-soluble or water-dispersible stains, and a combination of washing with water or hot water is required. As a more preferable cleaning method in such cases, a method is known in which water is emulsified in Freon 113 in a w/o type and a composition is used which sufficiently removes water-soluble or water-dispersible stains. Various proposals have been made for compositions in which water is emulsified in Freon 113, and for emulsifiers used in such compositions, such as those disclosed in Japanese Patent Publication No. 44-8973, Japanese Patent Publication No. 31471-1973, etc. . However, in these compositions, the emulsifier is limited to one or two types, and when other substances are added, the amount of water emulsified decreases considerably, and furthermore, the amount of water emulsified decreases significantly even when the temperature decreases. .
It also has the disadvantage of corroding zinc and copper products. As a result of extensive research in view of the above-mentioned problems, the inventor of the present invention has found that by using multiple emulsifiers in combination to emulsify water into Freon 113, it is possible to emulsify a large amount of water with a small amount of emulsifier. Based on this knowledge, they discovered that the degree of temperature dependence on the amount of water emulsified can be made smaller, and that the addition of a specific stabilizer shows remarkable stability for zinc and copper products. As a result, the present invention was completed. That is, the first aspect of the present invention is a water-in-oil emulsion consisting of 0.25 to 50% by weight of water and at least 30% by weight of 1,1,2-trichloro-1,2,2-trifluoroethane, The following ingredients: 0.08-36% by weight of dodecylbenzenesulfonic acid isopropylamine salt and at least one of sorbitan fatty acid ester and polyoxyethylene sorbitan fatty acid ester.
This is a cleaning emulsion composition containing 0.02 to 9% by weight of seeds. The second aspect of the present invention is to add to the composition as stabilizers: 0.01 to 0.5% by weight of nitroalkanes, benzotriazoles, mercaptobenzimidazole,
At least one of mercaptobenzoxazole and mercaptobenzothiazole from 0.005
This is a cleaning emulsion composition containing 0.05% by weight. Sorbitan fatty acid ester and polyoxyethylene sorbitan fatty acid ester used in the present invention are compounds represented by the following formulas [] and [], respectively, and in the formula are saturated and unsaturated aliphatic hydrocarbons,
Further, l, m, and n shown in parentheses can take any integer value, but it is preferable that each has an HLB value of 6 to 14. In the present invention, dodecylbenzenesulfonic acid isopropylamine salt and sorbitan derivatives are used together as emulsifiers, but dodecylbenzenesulfonic acid isopropylamine salt alone has a relatively large maximum emulsification amount, but the stable emulsification range is narrow; By using sorbitan derivatives in combination, the maximum amount of emulsification can be increased, and at the same time, it is possible to emulsify stably in all regions up to the maximum amount of emulsification. Furthermore, the emulsification range can be expanded by adding a basic nitrogen-containing compound as an emulsion aid, and the addition of this compound is also preferred. As the basic nitrogen-containing compound used here, all of aliphatic primary, secondary, and tertiary amines, alicyclic amines, aromatic amines, ammonia, etc. can be employed. The amount added is preferably in the range of 0.00005 to 0.0005 mol per 100 g of the emulsion composition. In the present invention, the amount of water is preferably 0.25 to 50% by weight; if it exceeds 50% by weight, the emulsion changes from a water-in-oil type to an oil-in-water type, which is not preferred. Further, if the amount is less than 0.25% by weight, it is not practical or preferable for use in removing water-soluble or water-dispersible stains. In addition, to take advantage of the characteristics of Freon-113, it is necessary to
The amount of 113 must be at least 30% by weight, and dodecylbenzenesulfonic acid isopropylamine salt has a practical lower limit of 0.25% by weight of water and an upper limit of 50% by weight.
The amount range required to emulsify 0.05 to 12% by weight is applied. Although it is not particularly necessary to use 12% by weight or more from the viewpoint of water emulsion stability, there is no particular problem even if the amount exceeds this. Sorbitan derivatives are usually 20 to 30
Approximately % by weight is preferable, and the amount added is 0.01 to 4
Used in a range of % by weight. The second aspect of the present invention is a composition to which a stabilizer is added, especially for use in zinc products and copper products without corrosion, and includes benzotriazoles, mercaptobenzimidazoles, mercaptobenzoxazoles, and mercaptobenzothiazoles. It is characterized by the combined use of at least one of these and a nitroalkane. As the benzotriazole, methylbenzotriazole, 5-nitrobenzotriazole, etc. having an alkyl substituent can also be employed, but benzotriazole itself without a substituent is preferred. Furthermore, mercaptobenzimidazoles, mercaptobenzoxazoles, and mercaptobenzothiazoles having substituents can also be used, and each of these may be used alone or two or more types may be used in combination. It's okay. The amount of these stabilizers added is 0.005 to the emulsion.
The range of 0.05% by weight or less is preferable; if it is less than 0.005% by weight, the stabilizing effect will not be sufficiently exhibited, and if it is added more than 0.05% by weight, there is no particular benefit and there is no need for it. As the nitroalkanes used in the present invention, nitromethane and nitroethane are preferable, but 2-nitropropane and the like can also be used, and are usually selected from nitroalkanes having 1 to 3 carbon atoms, and the amount added. is 0.01 to emulsion
A range of 0.5% by weight is preferable; if it is less than 0.01% by weight, the effect cannot be obtained, and even if it is added more than 0.5% by weight, no particularly excellent effect can be expected and there is no need to add it. Next, the present invention will be explained in detail with reference to Examples. Examples 1 to 6, Comparative Examples 1 and 2 Dodecylbenzenesulfonic acid isopropylamine salt (DBS-salt), sorbitan monolaurate and polyoxyethylene sorbitan oleate as sorbitan derivatives were added to 100 parts by weight of Freon 113 in various amounts. amount of the composition, and furthermore, the composition
Add 0.01 parts by weight of a basic nitrogen-containing compound to 100 parts by weight to adjust the stable emulsification range of water to 10°C, 25°C, and 35°C.
It was measured with The results are shown in Table 1.

【表】【table】

【表】 実施例7、比較例3 ドデシルベンゼンスルホン酸イソプロピルアミ
ン塩2.0gr、ソルビタンモノラウレート0.5gr、シ
クロヘキシルアミン0.01gr、水6gr、フロン113
91.49gからなる組成物にニトロメタン、ベンゾ
トリアゾール、メルカプトベンゾイミダゾール、
メルカプトベンゾオキサゾール、メルカプトベン
ゾチアゾールを第2表の如く添加して得た乳濁液
を十分研摩した亜鉛板または銅板を30℃にて100
時間浸漬したのち、亜鉛板と銅板の腐食状態及び
組成物の外観変化を調べた結果を第2表に示す。
[Table] Example 7, Comparative Example 3 Dodecylbenzenesulfonic acid isopropylamine salt 2.0gr, sorbitan monolaurate 0.5gr, cyclohexylamine 0.01gr, water 6gr, Freon 113
A composition consisting of 91.49g of nitromethane, benzotriazole, mercaptobenzimidazole,
An emulsion obtained by adding mercaptobenzoxazole and mercaptobenzothiazole as shown in Table 2 was thoroughly polished on a zinc or copper plate at 30°C for 100°C.
Table 2 shows the results of examining the corrosion state of the zinc plate and copper plate and changes in the appearance of the composition after being immersed for a period of time.

【表】【table】

Claims (1)

【特許請求の範囲】 1 0.25〜50重量%の水と、少なくとも30重量%
の1,1,2―トリクロロ―1,2,2―トリフ
ルオロエタンからなる油中水型乳濁液において、
次の成分: ドデシルベンゼンスルホン酸イソプロピルア
ミン塩0.08〜36重量%と ソルビタン脂肪酸エステル、ポリオキシエチ
レンソルビタン脂肪酸エステルの少なくとも1
種0.02〜9重量%とを含む洗浄用乳濁液組成
物。 2 0.25〜50重量%の水と、少なくとも30重量%
の1,1,2―トリクロロ―1,2,2―トリフ
ルオロエタンからなる油中水型乳濁液において、
次の成分: ドデシルベンゼンスルホン酸イソプロピルア
ミン塩0.08〜36重量%と ソルビタン脂肪酸エステル、ポリオキシエチ
レンソルビタン脂肪酸エステルの少なくとも1
種0.02〜9重量%と ニトロアルカン類0.01〜0.5重量%とベンゾ
トリアゾール類、メルカプトベンゾイミダゾー
ル、メルカプトベンゾオキサゾールおよびメル
カプトベンゾチアゾールのうち少なくとも1種
0.005〜0.05重量%とを含む洗浄用乳濁液組成
物。
[Claims] 1. 0.25 to 50% by weight of water and at least 30% by weight.
In a water-in-oil emulsion consisting of 1,1,2-trichloro-1,2,2-trifluoroethane,
The following ingredients: 0.08-36% by weight of dodecylbenzenesulfonic acid isopropylamine salt and at least one of sorbitan fatty acid ester and polyoxyethylene sorbitan fatty acid ester.
A cleaning emulsion composition comprising 0.02 to 9% by weight of a species. 2 0.25-50% water and at least 30% by weight
In a water-in-oil emulsion consisting of 1,1,2-trichloro-1,2,2-trifluoroethane,
The following ingredients: 0.08-36% by weight of dodecylbenzenesulfonic acid isopropylamine salt and at least one of sorbitan fatty acid ester and polyoxyethylene sorbitan fatty acid ester.
0.02 to 9% by weight of seeds, 0.01 to 0.5% by weight of nitroalkanes, and at least one of benzotriazoles, mercaptobenzimidazole, mercaptobenzoxazole, and mercaptobenzothiazole.
A cleaning emulsion composition comprising 0.005 to 0.05% by weight.
JP14057583A 1983-08-02 1983-08-02 Emulsion composition for detergent Granted JPS6032898A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14057583A JPS6032898A (en) 1983-08-02 1983-08-02 Emulsion composition for detergent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14057583A JPS6032898A (en) 1983-08-02 1983-08-02 Emulsion composition for detergent

Publications (2)

Publication Number Publication Date
JPS6032898A JPS6032898A (en) 1985-02-20
JPS6311400B2 true JPS6311400B2 (en) 1988-03-14

Family

ID=15271874

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14057583A Granted JPS6032898A (en) 1983-08-02 1983-08-02 Emulsion composition for detergent

Country Status (1)

Country Link
JP (1) JPS6032898A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100454954B1 (en) * 2001-12-05 2004-11-06 삼성전자주식회사 Amplitude mask and demultiplexer applied long-period optical fiber gratings fabricated by the same

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL154782A0 (en) * 2003-03-06 2003-10-31 J G Systems Inc Chemical-mechanical polishing composition containing organic nitro compounds
US7148147B2 (en) 2003-03-06 2006-12-12 J.G. Systems, Inc. CMP composition containing organic nitro compounds
CN102993807A (en) * 2012-09-29 2013-03-27 蔡丛荣 Preparation and application of aluminium alloy surface anti-corrosion and color-fixing agent

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4932183A (en) * 1972-07-25 1974-03-23
JPS5141106B2 (en) * 1973-11-27 1976-11-08

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100454954B1 (en) * 2001-12-05 2004-11-06 삼성전자주식회사 Amplitude mask and demultiplexer applied long-period optical fiber gratings fabricated by the same

Also Published As

Publication number Publication date
JPS6032898A (en) 1985-02-20

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