JPH05269301A - Dewatering fluorosolvent - Google Patents

Abstract

PURPOSE:To obtain a dewatering solvent without depleting the ozone layer and having an excellent dewatering power by incorporating nonafluoropentane expressed by a specified general formula into the solvent as the effective component. CONSTITUTION:This dewatering solvent is obtained by adding at least one kind selected from alcohols, ketones and surfactant to nonafluoropentane expressed by C5H3F9. 1H-, 2H- and 3H-perfluoropentane, 1H-, 3H- and 5H- perfluoropentane, 1H-, 1H- and 5H-perfluoropentane, 2H-, 2H- and 4H- perfluoropentane, etc., are exemplified as the nonafluoropentane. A <=8C alcohol is preferably used as the alcohol, and methanol, ethanol, isopropyl alcohol, etc., are exemplified. A <=9C ketone is preferably used as the ketone, and acetone, methyl ethyl ketone, etc., are exemplified.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION The present invention relates to precision instruments, optical instruments,
The present invention relates to a draining solvent that removes water adhering to the surface of a component such as an electronic device after washing the component with water.

[0002]

2. Description of the Related Art When cleaning parts such as precision equipment, optical equipment, and electronic equipment, a method of cleaning with pure water after treatment with a suitable detergent suitable for contaminants is widely used. A drying step is required to remove the water present on the article surface. As a drying means, physical methods such as heating, decompression, and centrifugation have been used for a long time, but in recent years, a drying method using a solvent that has a low energy cost and is capable of high-speed drying has become widespread. As a solvent, a liquid obtained by adding a surfactant or ethanol to trichlorotrifluoroethane (hereinafter referred to as Freon R113) is widely used.

[0003]

Fluorocarbon R113 has a lot of excellent properties such as nonflammability, low toxicity and low surface tension, and thus the demand has rapidly increased, but it is chemically stable and within the troposphere. It has been pointed out in recent years that it has a long lifespan and that it reaches the stratosphere, destroys the ozone layer, and increases harmful ultraviolet rays that reach the surface of the earth, resulting in a serious impact on the earth's ecosystem, including humankind.

For this reason, there is an active international movement to regulate the production and consumption of CFCs such as CFC R113 having a high ozone depletion potential and to abolish them. In order to cope with such a situation, the present invention provides a novel draining solvent which does not destroy the ozone layer and has a draining ability comparable to that of conventional draining agents.

[0005]

As a result of intensive studies, the present inventors have found that nonafluoropentane represented by the general formula C ₅ H ₃ F ₉ is at least selected from alcohols, ketones, and surfactants. The inventors have found that the above problems can be achieved by adding one kind, and have reached the present invention. Examples of the nonafluoropentane represented by the general formula C ₅ H ₃ F ₉ include 1H, 2H, 3H-perfluoropentane, 1H, 3H, 5H-perfluoropentane, 1H,
1H, 5H-perfluoropentane, 2H, 2H, 4H
-Perfluoropentane and the like can be mentioned.

The compound of the present invention represented by the general formula C ₅ H ₃ F ₉ can be produced by a known method. For example, 1H,
2H, 3H-perfluoropentane is trifluoroethylene to which 1,1,1,2,2,3-hexafluoropropane is added, and 1H, 3H, 5H-perfluoropentane is 1,2-difluorofluoromethane. After addition of 2 moles of diiodoethane, reduction, 2H, 2H, 4H-perfluoropentane was converted to hexafluoropropene (HF).
1,1,1-trifluoroethane is added to P), 1H,
1H, 5H-perfluoropentane is 2,2,3,
It can be synthesized by tosylating 3,4,4,5,5-octafluoropentanol followed by fluorination.

Alcohols having 8 or less carbon atoms are preferable, for example, methanol, ethanol, 1-
Propanol, isopropanol, 1-butanol, 2
-Butanol, isobutanol, t-butanol, 1-
Pentanol, 2-pentanol, 3-pentanol,
2-methyl-1-butanol, isopentyl alcohol, t-pentyl alcohol, 3-methyl-2-butanol, neopentyl alcohol, 1-hexanol, 2
-Methyl-1-pentanol, 4-methyl-2-pentanol, 2-ethyl-1-butanol, 1-heptanol, 2-heptanol 3-heptanol, 1-octanol, 2-octanol, 2-ethyl-1- Hexanol, cyclohexanol, methylcyclohexanol,
2,2,2-trifluoroethanol, 1H, 1H-pentafluoro-1-propanol, 2,2,3,3-tetrafluoro-1-propanol, 1H, 1H-pentafluoro-1-butanol, ethylene glycol, Propylene glycol and the like can be mentioned. More preferable are methanol, ethanol, isopropanol and the like. The amount of alcohol added is 0 to 30% by weight, preferably 0 to
It is 20% by weight, more preferably 0 to 15% by weight.

The ketones preferably have 9 or less carbon atoms, for example, acetone, methyl ethyl ketone, 2
-Pentanone, 2-hexanone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone, methyl cyclohexanone and the like. Acetone, methyl ethyl ketone and the like are more preferable. The amount of ketones added is 0 to 30% by weight, preferably 0 to 20% by weight.
The total addition amount of alcohols and ketones is 0 to 50% by weight, preferably 0 to 30% by weight, more preferably 0 to 2%.
It is 0% by weight.

As the surface active agent, known anionic surface active agents, cationic surface active agents, nonionic surface active agents and amphoteric surface active agents can be used. Examples of the anionic activator include carboxylate,
Examples thereof include sulfonate, sulfate ester salt, and phosphate ester salt. Examples of the cationic activator include salts of amines with various acids and quaternary ammonium salts. Examples of the nonionic activator include polyoxyethylene ether, polyoxyethylene-polyoxypropylene glycol, polyoxyethylene-polyoxypropylene alkyl ether, and fatty acid partial ester of polyhydric alcohol. Examples of the amphoteric activator include betaine type, amino organic acid type, and fatty acid amine salts. Activators containing a fluorine atom in the molecule of these compounds are also suitable. The amount of these surfactants added is 0 to 10% by weight, preferably 0 to 5% by weight.

[0010]

EXAMPLES Hereinafter, examples will be described. Examples 1 to 24 100 g of glass beads having a diameter of 0.8 mm and a diameter of 40 m
It was placed in a wire mesh basket (30 mesh) having a height of m and a height of 60 mm, and the whole basket was immersed in water colored with a dye, and then immersed in 500 ml of a draining solvent placed in a beaker for 2 minutes, and the residual state of water was visually observed. .. The results are shown in Tables 1 to 4.

[0011]

[Table 1]

[0012]

[Table 2]

[0013]

[Table 3]

[0014]

[Table 4]

[0015]

As is clear from the examples, the water-removing solvent of the present invention is useful as a solvent replacing the water-removing solvent using CFC 113, which has a high ozone depleting ability.

 ─────────────────────────────────────────────────── ─── Continuation of the front page (31) Priority claim number Japanese Patent Application No. 4-14074 (32) Priority Day Hei 4 (1992) January 29 (33) Priority claim country Japan (JP)

Claims (1)

[Claims] 1. A draining solvent containing nonafluoropentane represented by the general formula C ₅ H ₃ F ₉ as an active ingredient.