JPS5861198A - Chlorinated hydrocarbon mixed solvent composition - Google Patents

Chlorinated hydrocarbon mixed solvent composition

Info

Publication number
JPS5861198A
JPS5861198A JP16030081A JP16030081A JPS5861198A JP S5861198 A JPS5861198 A JP S5861198A JP 16030081 A JP16030081 A JP 16030081A JP 16030081 A JP16030081 A JP 16030081A JP S5861198 A JPS5861198 A JP S5861198A
Authority
JP
Japan
Prior art keywords
mixed solvent
dichloropropane
chlorinated hydrocarbon
solvent composition
methylene chloride
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
JP16030081A
Other languages
Japanese (ja)
Inventor
大石 和男
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.)
AGC Inc
Original Assignee
Asahi 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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP16030081A priority Critical patent/JPS5861198A/en
Publication of JPS5861198A publication Critical patent/JPS5861198A/en
Pending legal-status Critical Current

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  • Detergent Compositions (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、塩素化炭化水素系混合溶剤組成物に関するも
のであシ、詳しくはメチレンクロライドの特定量を添加
混合したジクロルグロバ/溶剤に関するものである。・ 従来より、金属洗浄用あるいはドライクリーニング用等
の溶剤として、メチレンクロライド。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a chlorinated hydrocarbon mixed solvent composition, and more particularly to a dichlorogloba/solvent mixed with a specific amount of methylene chloride.・Methylene chloride has traditionally been used as a solvent for metal cleaning and dry cleaning.

トリクロールエチレン、パークロルエチレンあるいはメ
チルクロロホルム等の塩素化炭化水素系溶剤が商業的に
広く利用されている。近年、石油化学工業の発展により
、エチレンの塩素誘導体と共に、C8留分の利用として
プロピレンの塩素誘導体が多量に使われている。例えば
、クロルヒドリン法によるプロピレンからプロピレンオ
キサイドを製造する場合等である。かかる場合、副生物
としてジクロルプロパンが相当量で得られる事が知られ
ており、該副生ジクロルプロパンの用途開発が切望され
ている。
Chlorinated hydrocarbon solvents such as trichlorethylene, perchlorethylene or methylchloroform are widely used commercially. In recent years, with the development of the petrochemical industry, chlorine derivatives of propylene are being used in large quantities as C8 fractions, along with chlorine derivatives of ethylene. For example, this is the case when propylene oxide is produced from propylene by the chlorohydrin method. In such cases, it is known that a considerable amount of dichloropropane is obtained as a by-product, and there is a strong desire to develop uses for this by-product dichloropropane.

本発明者は、かかるジクロルプロパンを従来の塩素系溶
剤のごとく洗浄用溶剤としての用途を開拓するため種々
の研究、検討を進めてきた。
The present inventor has conducted various studies and studies in order to develop the use of dichloropropane as a cleaning solvent like conventional chlorinated solvents.

その結果、ジクロルプロパン単独では洗浄用溶剤として
満足し得る洗浄力金示さないばかりか、引火の危険や毒
性あるいは臭気の問題が認められた。そこで、かかる欠
点を解消するべく更に検討を進めたところ、次のような
新規な事項を見出すに至った。すなわち、ジクロルプロ
パンに特定量以上のメチレンクロライドを添加混合する
ことによシ、ジクロルプロパン単独時よシ、大幅に洗浄
力が改善できるとともに、引火の危険がなく、毒性や臭
気をも改善することができ、商業的に充分使い得る溶剤
となし得ることを見出したものである。
As a result, it was found that dichloropropane alone does not exhibit sufficient cleaning power as a cleaning solvent, and also poses problems of flammability, toxicity, and odor. Therefore, as a result of further investigation in order to resolve these drawbacks, we discovered the following new matter. In other words, by adding and mixing more than a certain amount of methylene chloride to dichloropropane, cleaning power can be significantly improved compared to using dichloropropane alone, and there is no risk of ignition, and toxicity and odor are also improved. It has been discovered that the solvent can be used commercially.

このように、本発明は、前記のごとき問題点の認識なら
びに新・規事実の発見に基いて完成されたものであり、
ジクロルプロパン及びメチレンクロライドからなる新規
な塩素化炭化水素系混合溶剤を提供するものである。
In this way, the present invention was completed based on the recognition of the above-mentioned problems and the discovery of new and novel facts.
A novel chlorinated hydrocarbon mixed solvent consisting of dichloropropane and methylene chloride is provided.

本発明の混合溶剤は、通常はジクロルプロパン1重量部
に対してメチレンクロライド全0.3重量部以上添加混
合することにより、好ましくU 0.4重量部以上添加
混合することにより、商業的利用に対して満足し得るも
のとなる。例えば、混合溶剤中にジクロルプロパン70
重量%。
The mixed solvent of the present invention can be used commercially by usually adding 0.3 parts by weight or more of methylene chloride to 1 part by weight of dichloropropane, preferably adding and mixing 0.4 parts by weight or more of U. be satisfied with. For example, 70% dichloropropane in a mixed solvent.
weight%.

メチレンクロライ)”30重量%含む組成物では、引火
点は存在せず、洗浄力の目安となるカウリブタノール値
がパークロルエチレンよりも高く、許容濃度をメチルク
ロロホルム並に改善することができる。ジクロルプロパ
ンにd、1.2−ジクロルプロパン、ll3−ジクロル
プロパン。
In a composition containing 30% by weight of ``methylene chloride'', there is no flash point, the value of kauributanol, which is a measure of detergency, is higher than that of perchlorethylene, and the allowable concentration can be improved to the same level as methyl chloroform. Dichloropropane, d, 1,2-dichloropropane, ll3-dichloropropane.

1、 l−ジクロルプロパン及び2,2−ジクロルプロ
パンがあるが、いずれも使用可能である。
There are 1,1-dichloropropane and 2,2-dichloropropane, both of which can be used.

又、気液相が共存する、特に金属の脱脂洗浄に使用する
場合には、溶剤の分解を抑制し得るような安定剤を含有
せしめる事が望ましい。かかる安定剤としては、従来よ
りメチレンクロライドやパークロルエチレンの如き塩素
化炭化水素系溶剤の安定剤として知られているもの等を
適宜使用できる。例えば、アルコール類、エポキシド類
、ニトロアルカン類、エーテル類、フェノール類あるい
はアミン類である。さらに、本願発明の混合溶剤におい
ては、ジクロルプロパン及びメチレンクロライドの他に
、前記安定剤の他、本発明の目的を阻害しない範囲内で
、他の溶剤や種々の添加剤を添加混合使用する事も勿論
差支えない。
In addition, especially when used for degreasing and cleaning metals in which a gas-liquid phase coexists, it is desirable to contain a stabilizer capable of suppressing decomposition of the solvent. As such stabilizers, those conventionally known as stabilizers for chlorinated hydrocarbon solvents such as methylene chloride and perchloroethylene can be used as appropriate. For example, alcohols, epoxides, nitroalkanes, ethers, phenols or amines. Furthermore, in the mixed solvent of the present invention, in addition to dichloropropane and methylene chloride, other solvents and various additives may be added and mixed in addition to the above-mentioned stabilizers within a range that does not impede the purpose of the present invention. Of course, there is no difference.

本発明の混合溶剤は、一般機械、金属用の洗浄溶剤や塗
料剥離剤その他一般工業用溶剤として使用できる。特に
引火による爆発や火災の危険が伴う使用形態において、
あるいは半密閉。
The mixed solvent of the present invention can be used as a cleaning solvent for general machinery and metals, a paint stripper, and other general industrial solvents. Especially in usage situations where there is a risk of explosion or fire due to ignition.
Or semi-closed.

オーブン型使用であって毒性の影響゛を無視できない使
用形態において本発明の混合溶剤は有利である。
The mixed solvent of the present invention is advantageous in oven-type usage where the effects of toxicity cannot be ignored.

次に本発明の実施例について具体的に説明するが、かか
る説明によって本発明が何ら限定されるものでないこと
は勿論である。尚、以下の実施例において、第1表のカ
ウリブタノール値の測定は、トルエンを標準とする方法
を用いるASTM : D 1133−61に従った0
また引火点の測定K ハ、r工s K 2265ベンス
キ一マルテンス式(密閉型)引火点測定器を用いた。第
2表の安定性試験は、r工EIK 1508に基づき還
流冷却器、酸素導入管を備えた三角フラスコに試料20
0−を入れ、これによく磨いた軟鋼片1個を試料液中に
、他の軟鋼片】8個を液面の上部的3mの蒸気中に吊り
下け、水分を飽和させた酸素ガスを毎分10〜15個の
気泡の割合で内径3Mのガラス管から吹き込む。フラス
コ底部から150Wの電球で加熱し、48時間加熱還流
を続けるQ試験後、試料を室温まで冷却し、その40f
を採取して、これに中性蒸留水409をカロえ、3、分
間はげしく攪拌した後、水層4Of’にとシpHe測定
する。更にその液についてN/′100NaO1(ある
いはN/100HCIにて中和滴定を行ない酸度あるい
はアルカリ度を測定し次。
Next, examples of the present invention will be specifically described, but it goes without saying that the present invention is not limited by such description. In addition, in the following examples, the measurement of the caulibutanol value in Table 1 was performed according to ASTM: D 1133-61 using a method using toluene as the standard.
Further, the flash point was measured using a K 2265 Benski-Martens type (closed type) flash point measuring device. The stability test in Table 2 was conducted based on EIK 1508, in which sample 20 was placed in an Erlenmeyer flask equipped with a reflux condenser and an oxygen inlet tube.
0-, one well-polished mild steel piece was suspended in the sample solution, and the other 8 pieces were suspended in steam 3 m above the liquid level, and oxygen gas saturated with moisture was added. Blow through a glass tube with an internal diameter of 3M at a rate of 10-15 bubbles per minute. After the Q test in which the flask was heated with a 150W light bulb and heated under reflux for 48 hours, the sample was cooled to room temperature and the 40F
After adding neutral distilled water 409 to it and stirring vigorously for 3 minutes, the pH of the aqueous layer 4Of' was measured. Further, the solution was subjected to neutralization titration with N/'100 NaO1 (or N/100 HCI) to measure acidity or alkalinity.

Claims (1)

【特許請求の範囲】 1)ジクロルプロパン及びメチレンクロライドからなる
ことを特徴とする塩素化炭化水素系混合溶剤組成物。 2)ジクロルプロパン1重量部に対して0.3重量部以
上のメチレンクロライドからなる特許請求の範囲第1項
記載の混合溶剤組成物。
[Scope of Claims] 1) A chlorinated hydrocarbon mixed solvent composition comprising dichloropropane and methylene chloride. 2) The mixed solvent composition according to claim 1, comprising 0.3 parts by weight or more of methylene chloride per 1 part by weight of dichloropropane.
JP16030081A 1981-10-09 1981-10-09 Chlorinated hydrocarbon mixed solvent composition Pending JPS5861198A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16030081A JPS5861198A (en) 1981-10-09 1981-10-09 Chlorinated hydrocarbon mixed solvent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16030081A JPS5861198A (en) 1981-10-09 1981-10-09 Chlorinated hydrocarbon mixed solvent composition

Publications (1)

Publication Number Publication Date
JPS5861198A true JPS5861198A (en) 1983-04-12

Family

ID=15711978

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16030081A Pending JPS5861198A (en) 1981-10-09 1981-10-09 Chlorinated hydrocarbon mixed solvent composition

Country Status (1)

Country Link
JP (1) JPS5861198A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0633384U (en) * 1992-10-01 1994-04-28 平河ヒューテック株式会社 Power cord molding frame

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4911555A (en) * 1972-05-02 1974-02-01
JPS4937632A (en) * 1972-08-08 1974-04-08
JPS503126A (en) * 1973-05-12 1975-01-14
JPS5487711A (en) * 1977-12-26 1979-07-12 Daikin Ind Ltd Solvent composition for cleaning

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4911555A (en) * 1972-05-02 1974-02-01
JPS4937632A (en) * 1972-08-08 1974-04-08
JPS503126A (en) * 1973-05-12 1975-01-14
JPS5487711A (en) * 1977-12-26 1979-07-12 Daikin Ind Ltd Solvent composition for cleaning

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0633384U (en) * 1992-10-01 1994-04-28 平河ヒューテック株式会社 Power cord molding frame

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