JP2651652B2 - Fluorinated alcohol-based cleaning agent - Google Patents

Fluorinated alcohol-based cleaning agent

Info

Publication number
JP2651652B2
JP2651652B2 JP13127693A JP13127693A JP2651652B2 JP 2651652 B2 JP2651652 B2 JP 2651652B2 JP 13127693 A JP13127693 A JP 13127693A JP 13127693 A JP13127693 A JP 13127693A JP 2651652 B2 JP2651652 B2 JP 2651652B2
Authority
JP
Japan
Prior art keywords
cleaning agent
hexafluoropropan
substrate
trifluoromethyl
cleaning
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 - Lifetime
Application number
JP13127693A
Other languages
Japanese (ja)
Other versions
JPH06346096A (en
Inventor
章 関屋
満 高橋
嘉彦 後藤
淳雄 須賀
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
National Institute of Advanced Industrial Science and Technology AIST
Tosoh Corp
AGC Inc
Original Assignee
Agency of Industrial Science and Technology
Asahi Glass Co Ltd
Central Glass Co Ltd
Tosoh 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 Agency of Industrial Science and Technology, Asahi Glass Co Ltd, Central Glass Co Ltd, Tosoh Corp filed Critical Agency of Industrial Science and Technology
Priority to JP13127693A priority Critical patent/JP2651652B2/en
Publication of JPH06346096A publication Critical patent/JPH06346096A/en
Application granted granted Critical
Publication of JP2651652B2 publication Critical patent/JP2651652B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/50Solvents

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は洗浄剤に関し、特に、半
導体製造工程で使用される基板等の洗浄に有効な洗浄剤
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cleaning agent, and more particularly to a cleaning agent effective for cleaning a substrate or the like used in a semiconductor manufacturing process.

【0002】[0002]

【従来の技術】ICやLSI等の半導体の製造に用いら
れるウエハー等の基板、フォトリソグラフィー工程で使
用されるマスクやレチクル及びその前駆体としての石英
基板等の基板、ペリクルを製造する際に使用されるガラ
ス基板、さらには、光ディスクの製造に用いるスタンパ
ーの製造に使用される基板等は、その性質上極めてきれ
いに洗浄されている必要がある。
2. Description of the Related Art Substrates such as wafers used in the manufacture of semiconductors such as ICs and LSIs, masks and reticles used in the photolithography process, and substrates such as quartz substrates used as precursors for the production of pellicles. The glass substrate to be manufactured, and furthermore, the substrate used for manufacturing a stamper used for manufacturing an optical disc, and the like, need to be extremely cleanly cleaned due to their properties.

【0003】このような基板の洗浄方法としては、従
来、超音波洗浄、ブラシ等によるこすり洗い又は硫酸−
過酸化水素水,水酸化アンモニウム−過酸化水素水等に
よる酸化洗浄等で大部分の汚れを除去した後、イソプロ
パノール、2,2,3,3,3−ペンタフルオロプロパ
ノール又はフロン等の洗浄溶媒蒸気中に基板を置き、基
板表面で蒸気を凝縮させて表面を洗い流し、基板の温度
が蒸気温度と等しくなった時点で乾燥状態となる蒸気洗
浄乾燥法が広く用いられている。
[0003] As a method for cleaning such a substrate, conventionally, ultrasonic cleaning, scrubbing with a brush or the like or sulfuric acid-
After removing most of the stains by oxidative washing with a hydrogen peroxide solution, ammonium hydroxide-hydrogen peroxide solution, etc., a washing solvent vapor such as isopropanol, 2,2,3,3,3-pentafluoropropanol or chlorofluorocarbon. A steam cleaning and drying method is widely used in which a substrate is placed inside, a vapor is condensed on the surface of the substrate, and the surface is washed away. When the temperature of the substrate becomes equal to the vapor temperature, the substrate is dried.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、上記の
洗浄乾燥法でイソプロパノールを用いた場合、イソプロ
パノールは可燃性であるため、洗浄工程中に火災,爆発
等の事故が発生しやすいという問題点がある。また、イ
ソプロパノール及び2,2,3,3,3−ペンタフルオ
ロプロパノールはその沸点が高く、エネルギー効率が悪
いという欠点がある。さらに、従来使用されてきたクロ
ロフルオロカーボンは大気中に放出された場合に、成層
圏のオゾン層を破壊し、その結果地球上の生態系に悪影
響を及ぼすことが指摘され、従来のこれらのフロンは生
産及び使用規制が実施されている。
However, when isopropanol is used in the above-mentioned washing and drying method, there is a problem that accidents such as fire and explosion are likely to occur during the washing process because isopropanol is flammable. . In addition, isopropanol and 2,2,3,3,3-pentafluoropropanol have the disadvantage that their boiling points are high and their energy efficiency is poor. In addition, it has been pointed out that conventionally used chlorofluorocarbons, when released into the atmosphere, destroy the stratospheric ozone layer and, as a result, adversely affect ecosystems on the planet. And use regulations are in place.

【0005】本発明は、以上の問題点に鑑みてなされた
ものであり、その目的は、火災や爆発等の事故を防止
し、消費エネルギーが少なく、しかも、地球上の生態系
に悪影響を及ぼさないような洗浄剤を提供することにあ
る。
The present invention has been made in view of the above problems, and has as its object to prevent accidents such as fire and explosion, consume less energy, and adversely affect the ecosystem on the earth. It is to provide such a cleaning agent.

【0006】[0006]

【課題を解決するための手段】本発明者等は、上記の如
き技術の現状に鑑み検討を重ねた結果、1,1,1,
3,3,3−ヘキサフルオロプロパン−2−オール、
1,1,1,3,3,4,4,4−オクタフルオロブタ
ン−2−オール、2−トリフルオロメチル−1,1,
1,3,3,3−ヘキサフルオロプロパン−2−オー
ル、2−トリフルオロメチル−1,1,1−トリフルオ
ロプロパン−2−オールが、不燃性で、かつ塩素原子を
含まないためオゾン層を破壊せず、大気寿命が短いため
地球温暖化への寄与を小さくすることができ、さらに、
低沸点であることから消費エネルギーの少ない極めて優
れた洗浄剤となることを見いだし、本発明を完成するに
至ったものである。
Means for Solving the Problems The present inventors have repeatedly studied in view of the current state of the art as described above, and as a result, 1,1,1,
3,3,3-hexafluoropropan-2-ol,
1,1,1,3,3,4,4,4-octafluorobutan-2-ol, 2-trifluoromethyl-1,1,
Ozone layer because 1,3,3,3-hexafluoropropan-2-ol and 2-trifluoromethyl-1,1,1-trifluoropropan-2-ol are nonflammable and contain no chlorine atom And the contribution to global warming can be reduced because of the short atmospheric life.
The inventors have found that the cleaning agent has a low boiling point and thus is an extremely excellent cleaning agent with low energy consumption, and has completed the present invention.

【0007】すなわち、本発明は、1,1,1,3,
3,3−ヘキサフルオロプロパン−2−オール、1,
1,1,3,3,4,4,4−オクタフルオロブタン−
2−オール、2−トリフルオロメチル−1,1,1,
3,3,3−ヘキサフルオロプロパン−2−オール又は
2−トリフルオロメチル−1,1,1−トリフルオロプ
ロパン−2−オールの少なくともいずれか1種を使用す
ることを特徴とするフッ素化アルコール系洗浄剤であ
る。
That is, the present invention relates to 1,1,1,3
3,3-hexafluoropropan-2-ol, 1,
1,1,3,3,4,4,4-octafluorobutane-
2-ol, 2-trifluoromethyl-1,1,1,
A fluorinated alcohol characterized by using at least one of 3,3,3-hexafluoropropan-2-ol and 2-trifluoromethyl-1,1,1-trifluoropropan-2-ol It is a system cleaning agent.

【0008】以下、本発明をさらに詳細に説明する。本
発明の洗浄剤として使用する1,1,1,3,3,3−
ヘキサフルオロプロパン−2−オール[分子式:CF3
CH(OH)CF3 ]、1,1,1,3,3,4,4,
4−オクタフルオロブタン−2−オール[分子式:CF
3 CH(OH)CF2 CF3 ]、2−トリフルオロメチ
ル−1,1,1,3,3,3−ヘキサフルオロプロパン
−2−オール[分子式:(CF3 3 COH]、2−ト
リフルオロメチル−1,1,1−トリフルオロプロパン
−2−オール[分子式:(CF3 2 (CH3 )CO
H]は、それぞれ表1に示す物性値を有し、いずれも不
燃性であり、洗浄乾燥工程での火災、爆発等の危険がな
い。
Hereinafter, the present invention will be described in more detail. 1,1,1,3,3,3- used as the cleaning agent of the present invention
Hexafluoropropan-2-ol [molecular formula: CF 3
CH (OH) CF 3 ], 1,1,1,3,3,4,4,4
4-octafluorobutan-2-ol [molecular formula: CF
3 CH (OH) CF 2 CF 3 ], 2-trifluoromethyl-1,1,1,3,3,3-hexafluoropropan-2-ol [molecular formula: (CF 3 ) 3 COH], 2-trimethyl Fluoromethyl-1,1,1-trifluoropropan-2-ol [molecular formula: (CF 3 ) 2 (CH 3 ) CO
H] have the physical properties shown in Table 1 and are all nonflammable, and there is no danger of fire, explosion, etc. in the washing and drying process.

【0009】[0009]

【表1】 [Table 1]

【0010】なお、比較のためフロン113[CFC−
113]、2,2,3,3,3−ペンタフルオロプロパ
ノール[分子式:CF3 CF2 CH2 OH]及びイソプ
ロパノールの対応する物性値を表1にあわせて示す。
For comparison, Freon 113 [CFC-
113], 2,2,3,3,3-pentafluoropropanol [molecular formula: CF 3 CF 2 CH 2 OH] and the corresponding physical properties of isopropanol are also shown in Table 1.

【0011】本発明の洗浄剤として使用する1,1,
1,3,3,3−ヘキサフルオロプロパン−2−オー
ル、1,1,1,3,3,4,4,4−オクタフルオロ
ブタン−2−オール、2−トリフルオロメチル−1,
1,1,3,3,3−ヘキサフルオロプロパン−2−オ
ール、2−トリフルオロメチル−1,1,1−トリフル
オロプロパン−2−オールは、それぞれ単独で使用して
も又はこれらの混合物として使用してもよい。混合して
使用する際の混合比は、混合する物質によっても異なり
特に限定するものではないが、製造法に起因する経済性
を考慮して混合することが好ましく、例えば、2種類の
混合物の場合には1:5〜5:1があげられる。なお、
回収再利用等の経済性の面からは、単独で用いることが
特に好ましい。
The 1,1, used as the cleaning agent of the present invention
1,3,3,3-hexafluoropropan-2-ol, 1,1,1,3,3,4,4,4-octafluorobutan-2-ol, 2-trifluoromethyl-1,
1,1,3,3,3-Hexafluoropropan-2-ol and 2-trifluoromethyl-1,1,1-trifluoropropan-2-ol may be used alone or as a mixture thereof. You may use as. The mixing ratio when mixed and used differs depending on the substances to be mixed, and is not particularly limited. However, it is preferable to mix them in consideration of the economy resulting from the production method. For example, in the case of two kinds of mixtures, Is 1: 5 to 5: 1. In addition,
From the viewpoint of economy such as recovery and reuse, it is particularly preferable to use it alone.

【0012】本発明の洗浄剤の洗浄対象となる被洗浄物
としては、1,1,1,3,3,3−ヘキサフルオロプ
ロパン−2−オール、1,1,1,3,3,4,4,4
−オクタフルオロブタン−2−オール、2−トリフルオ
ロメチル−1,1,1,3,3,3−ヘキサフルオロプ
ロパン−2−オール、2−トリフルオロメチル−1,
1,1−トリフルオロプロパン−2−オールに対して安
定なものからなるものであれば特に限定するものではな
いが、特に基板の洗浄に適している。基板としては、例
えば、ガラス、石英又はこれらの表面にクロム等を蒸着
させて被膜を形成したもの、樹脂又はこれらの上に回路
パターン等を有しているもの等をあげることができる。
このような被洗浄物としては具体的には、半導体の製造
に用いられるウエハー等の基板、フォトリソグラフィー
工程で使用されるマスクやレチクル及びその前駆体とし
ての石英基板、ペリクルを製造する際に使用されるガラ
ス基板並びに光ディスクの製造に用いるスタンパーの製
造に使用される基板等をあげることができる。
The object to be cleaned with the cleaning agent of the present invention includes 1,1,1,3,3,3-hexafluoropropan-2-ol, 1,1,1,3,3,4 , 4,4
-Octafluorobutan-2-ol, 2-trifluoromethyl-1,1,1,3,3,3-hexafluoropropan-2-ol, 2-trifluoromethyl-1,
The material is not particularly limited as long as it is stable to 1,1-trifluoropropan-2-ol, but is particularly suitable for cleaning a substrate. Examples of the substrate include, for example, glass, quartz, a substrate having a film formed by depositing chromium or the like on the surface thereof, a resin, or a substrate having a circuit pattern or the like thereon.
Specifically, such an object to be cleaned is used when manufacturing a substrate such as a wafer used in semiconductor manufacturing, a mask or reticle used in a photolithography process and a quartz substrate as a precursor thereof, and a pellicle. And a substrate used for manufacturing a stamper used for manufacturing an optical disk.

【0013】本発明の洗浄剤による洗浄方法は特に限定
するものではなく、洗浄剤中に被洗浄物を浸漬したり、
被洗浄物に洗浄剤をスプレーしたりする方法などによる
こともできるが、特に蒸気洗浄が好ましい。蒸気洗浄法
は洗浄剤の蒸気中に被洗浄物を入れて被洗浄物表面を洗
浄した後乾燥させる。
The method of cleaning with the cleaning agent of the present invention is not particularly limited, and the object to be cleaned can be immersed in the cleaning agent,
Although a method of spraying a cleaning agent onto an object to be cleaned can be used, steam cleaning is particularly preferable. In the steam cleaning method, an object to be cleaned is put into the vapor of a cleaning agent, and the surface of the object to be cleaned is washed and then dried.

【0014】その具体的な方法としては、従来法と同様
に、洗剤水溶液や超純水中に被洗浄物を浸して超音波振
動で被洗浄物に付着している異物を除去する方法、洗剤
水溶液や超純水を用いてPVA発泡体等のブラシでこす
り洗いする方法又は硫酸−過酸化水素水,水酸化アンモ
ニウム−過酸化水素水等の溶液中に被洗浄物を浸して酸
化反応で有機物を除去する方法等の前処理法により大部
分の汚れを除去した後、本発明の1,1,1,3,3,
3−ヘキサフルオロプロパン−2−オール、1,1,
1,3,3,4,4,4−オクタフルオロブタン−2−
オール、2−トリフルオロメチル−1,1,1,3,
3,3−ヘキサフルオロプロパン−2−オール、2−ト
リフルオロメチル−1,1,1−トリフルオロプロパン
−2−オールの少なくともいずれか1種で表されるフッ
素化アルコールからなる洗浄剤の蒸気中に被洗浄物を置
き被洗浄物表面で蒸気を凝縮させて被洗浄物表面を洗い
流し、被洗浄物の温度が蒸気の温度と等しくなった時点
で乾燥状態となり、洗浄乾燥を終わる。このような方法
を採用した場合、洗浄乾燥された基板表面には洗浄剤は
残留しない。また、洗浄後の乾燥にかかる時間も短く、
短時間で乾燥することができる。
As a specific method, as in the conventional method, a method of immersing an object to be cleaned in a detergent aqueous solution or ultrapure water to remove foreign substances adhering to the object to be cleaned by ultrasonic vibration, A method of scrubbing with a brush such as a PVA foam using an aqueous solution or ultrapure water, or immersing an object to be cleaned in a solution of sulfuric acid-hydrogen peroxide solution, ammonium hydroxide-hydrogen peroxide solution, etc., and oxidizing the organic material by an oxidation reaction. After removing most of the stains by a pre-treatment method such as a method for removing, a 1,1,1,3,3 of the present invention
3-hexafluoropropan-2-ol, 1,1,
1,3,3,4,4,4-octafluorobutane-2-
All, 2-trifluoromethyl-1,1,1,3
Vapor of a cleaning agent comprising a fluorinated alcohol represented by at least one of 3,3-hexafluoropropan-2-ol and 2-trifluoromethyl-1,1,1-trifluoropropan-2-ol The object to be washed is placed inside, the vapor is condensed on the surface of the object to be washed, and the surface of the object to be washed is washed away. When the temperature of the object to be washed becomes equal to the temperature of the steam, the object is brought into a dry state, and the washing and drying is completed. When such a method is adopted, no cleaning agent remains on the surface of the substrate that has been cleaned and dried. In addition, the time required for drying after washing is short,
It can be dried in a short time.

【0015】[0015]

【実施例】以下、実施例を用いて本発明を説明するが、
本発明はこれらの実施例に限定されるものではない。
Hereinafter, the present invention will be described with reference to Examples.
The present invention is not limited to these examples.

【0016】(実施例1〜4)レチクル用のガラス基板
について硫酸洗浄(120℃、5分)を行い、水洗(3
分)した後、さらに超音波洗浄(3分)を行った。この
予備洗浄の後、洗浄剤として表1に示す1,1,1,
3,3,3−ヘキサフルオロプロパン−2−オール(実
施例1)、1,1,1,3,3,4,4,4−オクタフ
ルオロブタン−2−オール(実施例2)、2−トリフル
オロメチル−1,1,1,3,3,3−ヘキサフルオロ
プロパン−2−オール(実施例3)、2−トリフルオロ
メチル−1,1,1−トリフルオロプロパン−2−オー
ル(実4例4)を用いて、蒸気乾燥法により基板の洗浄
乾燥を行い目視により観察した。その結果を表2に示
す。
(Examples 1 to 4) A reticle glass substrate was washed with sulfuric acid (120 ° C., 5 minutes) and washed with water (3
Min), and ultrasonic cleaning (3 min) was further performed. After this preliminary cleaning, 1,1,1,
3,3,3-hexafluoropropan-2-ol (Example 1), 1,1,1,3,3,4,4,4-octafluorobutan-2-ol (Example 2), 2- Trifluoromethyl-1,1,1,3,3,3-hexafluoropropan-2-ol (Example 3), 2-trifluoromethyl-1,1,1-trifluoropropan-2-ol (actual Using 4 Example 4), the substrate was washed and dried by a steam drying method and visually observed. Table 2 shows the results.

【0017】(実施例5)洗浄剤として1,1,1,
3,3,4,4,4−オクタフルオロブタン−2−オー
ル(60重量%)と2−トリフルオロメチル−1,1,
1,3,3,3−ヘキサフルオロプロパン−2−オール
(40重量%)からなる混合物を用いた以外は実施例1
と同様にして行った。その結果を表2にあわせて示す。
EXAMPLE 5 1,1,1,1 was used as a cleaning agent.
3,3,4,4,4-octafluorobutan-2-ol (60% by weight) and 2-trifluoromethyl-1,1,
Example 1 except that a mixture consisting of 1,3,3,3-hexafluoropropan-2-ol (40% by weight) was used.
Was performed in the same manner as described above. The results are shown in Table 2.

【0018】(実施例6)洗浄剤として1,1,1,
3,3,3−ヘキサフルオロプロパン−2−オール(7
0重量%)と2−トリフルオロメチル−1,1,1,
3,3,3−ヘキサフルオロプロパン−2−オール(3
0重量%)からなる混合物を用いた以外は実施例1と同
様にして行った。その結果を表2にあわせて示す。
Example 6 1,1,1,1 was used as a cleaning agent.
3,3,3-hexafluoropropan-2-ol (7
0% by weight) and 2-trifluoromethyl-1,1,1,1
3,3,3-hexafluoropropan-2-ol (3
(0% by weight) except that a mixture consisting of 0% by weight was used. The results are shown in Table 2.

【0019】(参考例)洗浄剤としてイソプロパノール
を用いた以外は実施例1と同様にして行った。その結果
を表2にあわせて示す。但し、このイソプロパノールは
可燃性であるため、火災,爆発等の危険性がある。
(Reference Example) The same procedure as in Example 1 was carried out except that isopropanol was used as a detergent. The results are shown in Table 2. However, since this isopropanol is flammable, there is a danger of fire and explosion.

【0020】(比較例)洗浄剤として2,2,3,3,
3−ペンタフルオロプロパノールを用いた以外は実施例
1と同様にして行った。その結果を表2にあわせて示
す。
Comparative Example 2, 2, 3, 3,
It carried out similarly to Example 1 except having used 3-pentafluoropropanol. The results are shown in Table 2.

【0021】[0021]

【表2】 [Table 2]

【0022】[0022]

【発明の効果】以上説明したように、本発明によれば不
燃性のフッ素化アルコールを使用するので、従来の方法
においてイソプロパノールを洗浄溶媒として用いた場合
に問題となる火災や爆発の危険を回避でき、また、2,
2,3,3,3−ペンタフルオロプロパノールよりいず
れも低沸点であることから、消費エネルギーが少なく、
かつ短時間で乾燥することができ、さらに従来の方法と
同等又はそれ以上の洗浄乾燥性で被洗浄物の洗浄乾燥を
行うことができる効果を有するものである。
As described above, according to the present invention, since a nonflammable fluorinated alcohol is used, the danger of fire or explosion which is a problem when isopropanol is used as a washing solvent in the conventional method is avoided. Yes, and 2,
Since it has a lower boiling point than 2,3,3,3-pentafluoropropanol, it consumes less energy,
In addition, it can be dried in a short time, and has an effect that the object to be cleaned can be washed and dried with a washing and drying property equal to or higher than that of the conventional method.

───────────────────────────────────────────────────── フロントページの続き (73)特許権者 000000044 旭硝子株式会社 東京都千代田区丸の内2丁目1番2号 (74)上記4名の代理人 弁理士 箕浦 清 (72)発明者 関屋 章 茨城県つくば市東1丁目1番地 工業技 術院物質工学工業技術研究所内 (72)発明者 高橋 満 東京都文京区本郷2−40−17 本郷若井 ビル 財団法人地球環境産業技術研究機 構内 (72)発明者 後藤 嘉彦 東京都文京区本郷2−40−17 本郷若井 ビル 財団法人地球環境産業技術研究機 構内 (72)発明者 須賀 淳雄 東京都文京区本郷2−40−17 本郷若井 ビル 財団法人地球環境産業技術研究機 構内 審査官 佐藤 修 (56)参考文献 特開 平4−127955(JP,A) 特開 平3−27328(JP,A) 特開 平3−27329(JP,A) 特開 平2−286794(JP,A) 特開 平3−14898(JP,A) 特開 平4−243504(JP,A) ──────────────────────────────────────────────────続 き Continued on the front page (73) Patent holder 000000044 Asahi Glass Co., Ltd. 2-1-2-2 Marunouchi, Chiyoda-ku, Tokyo (74) The above four agents Patent Attorney Kiyoshi Minoura (72) Inventor Akira Sekiya Ibaraki 1-1-1 Higashi, Tsukuba City, National Institute of Advanced Industrial Science and Technology (72) Inventor Mitsuru Takahashi 2-40-17 Hongo, Bunkyo-ku, Tokyo Hongo Wakai Building Foundation for Global Environmental Technology Research and Technology (72) Inventor Yoshihiko Goto Hongo Wakai Building, Hongo Wakai Building, 2-40-17 Hongo, Tokyo, Japan (72) Inventor Atsushi Suga 2-40-17 Hongo, Hongo, Bunkyo-ku, Tokyo Hongo Wakai Building Global Environmental Industrial Technology Examiner Osamu Sato on-site of research equipment (56) References JP-A-4-127955 (JP, A) JP-A-3-27328 (JP, A) JP-A JP-A-3-27329 (JP, A) JP-A-2-286794 (JP, A) JP-A-3-14898 (JP, A) JP-A-4-243504 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 1,1,1,3,3,4,4,4−オク
タフルオロブタン−2−オール、2−トリフルオロメチ
ル−1,1,1,3,3,3−ヘキサフルオロプロパン
−2−オール又は2−トリフルオロメチル−1,1,1
−トリフルオロプロパン−2−オールの少なくともいず
れか1種を使用することを特徴とするフッ素化アルコー
ル系洗浄剤。
1. A 1,1,1,3,3,4,4,4-octafluorobutan-2-ol, 2-trifluoromethyl-1,1,1,3,3,3-hexafluoropropane -2-ol or 2-trifluoromethyl-1,1,1
-A fluorinated alcohol-based detergent comprising at least one of trifluoropropan-2-ol.
JP13127693A 1993-05-07 1993-05-07 Fluorinated alcohol-based cleaning agent Expired - Lifetime JP2651652B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13127693A JP2651652B2 (en) 1993-05-07 1993-05-07 Fluorinated alcohol-based cleaning agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13127693A JP2651652B2 (en) 1993-05-07 1993-05-07 Fluorinated alcohol-based cleaning agent

Publications (2)

Publication Number Publication Date
JPH06346096A JPH06346096A (en) 1994-12-20
JP2651652B2 true JP2651652B2 (en) 1997-09-10

Family

ID=15054156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13127693A Expired - Lifetime JP2651652B2 (en) 1993-05-07 1993-05-07 Fluorinated alcohol-based cleaning agent

Country Status (1)

Country Link
JP (1) JP2651652B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE471366T1 (en) 2006-09-14 2010-07-15 Fujifilm Corp MEANS FOR REMOVING WATER FROM A SUBSTRATE, METHOD FOR WATER REMOVAL AND DRYING METHOD THEREOF
JP6010894B2 (en) * 2011-10-31 2016-10-19 セントラル硝子株式会社 Cleaning / drying agent and substrate cleaning / drying method using the same
JP2015108041A (en) * 2013-12-03 2015-06-11 ダイキン工業株式会社 Cleaning composition
EP3898797A4 (en) * 2018-12-21 2022-11-02 Honeywell International Inc. Foaming agent compositions containing 1,2,2-trifluoro-1-trifluoromethylcyclobutane, and methods of foaming

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02286794A (en) * 1989-04-28 1990-11-26 Daikin Ind Ltd Fluorinated alcoholic solvent
JPH0327329A (en) * 1989-06-23 1991-02-05 Asahi Glass Co Ltd Fluorinated hydrocarbon-based solvent composition
JPH0327328A (en) * 1989-06-23 1991-02-05 Asahi Glass Co Ltd Fluorinated hydrocarbon-based solvent composition
JPH0314898A (en) * 1990-04-24 1991-01-23 Mitsui Petrochem Ind Ltd Detergent
JPH04127955A (en) * 1990-09-20 1992-04-28 Daikin Ind Ltd Method for cleaning article surface
JPH04243504A (en) * 1991-01-25 1992-08-31 Asahi Chem Ind Co Ltd Azeotropic composition for drainage

Also Published As

Publication number Publication date
JPH06346096A (en) 1994-12-20

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