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Publication numberUS3789006 A
Publication typeGrant
Publication date29 Jan 1974
Filing date28 Jun 1971
Priority date7 Jul 1970
Also published asCA947006A1, DE2133852A1, DE2133852B2
Publication numberUS 3789006 A, US 3789006A, US-A-3789006, US3789006 A, US3789006A
InventorsMcmillan I, Prest J
Original AssigneeIci Ltd
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Solvent compositions
US 3789006 A
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Description  (OCR text may contain errors)

United States Patent 3,789,006 SOLVENT COMPOSITIONS Ian McMillan and Jeffrey Prest, Runcorn, England, assignors to Imperial Chemical Industries Limited, London, England No Drawing. Filed June 28, 1971, Ser. No. 157,737 Claims priority, application Great Britain, July 7, 1970, 32,949/70 Int. Cl. Clld 7/50 US. Cl. 252-171 3 Claims ABSTRACT OF THE DISCLOSURE A solvent composition which comprises a mixture of trichlorotrifluoroethane, isopropanol and nitromethane, which mixture forms an azeotrope.

This invention relates to a cleaning composition comprising trichlorotrifluoroethane.

It is known that 1,l,2-trichloro-l,2,2-trifluoroethane, on account of its selective solvent power, is useful as a cleaning liquid for the removal of contaminants from a variety of articles and materials, particularly synthetic organic polymers and plastics which are themselves sensitive to other more common and more powerful solvents, such as trichloroethylene or perchloroethylene. However the use of 1,1,2-trichloro-1,2,-trifluoroethane on its own is often insuflicient to remove some of the more persistent forms of contamination, for example various active resinbased soldering fluxes. Some improvement in the efliciency of removal of such persistent contamination may be effected by the use of mechanical aids, for example boiling solvent or ultrasonic irradiation, but use of these mechanical aids is not always suflicient to remove all of the contamination.

We have now found that an improved cleaning fluid may be made by the addition of isopropanol and nitromethane to trichlorotrifluoroethane.

Thus according to the invention there is provided a solvent composition which comprises an azeotropic mixture of trichlorotrifluoroethane with isopropanol and nitromethane.

Preferably, the trichlorotrifluoroethane is 1,1,2-trichloro-l,2,2-trifluoroethane. The azeotropic mixture comprising this isomer contains about 95.5% by weight of 1,1,2- trichloro-1,2,2-trifluoroethane, about 2.5% by weight of isopropanol and about 2% by weight of nitromethane and has a boiling point at 760 mm. Hg of 45.87 C.

The cleaning compositions of the invention will remove some contaminants which are not removed by 1,1,2-trichloro-1,2,2-trifluoroethane alone. In processes which use a cleaning fluid, it is usually necessary from time to time to remove contamination from the liquid by distillation. Such distillations will normally be repeated many times during the useful life of the fluid and if the cleaning fluid consists of two different liquids having diiferent boiling points these distillations will tend to result in a concentration of one of the liquids and a change of the composition in the cleaning bath. Such a change of composition will cause a change in the solvent power of the cleaning fluid and may result in damage to the articles being cleaned or in the production of a dangerously inflammable mixture. However, by use of essentially azeotropic mixtures it is possible to avoid any risk of such undesirable consequences, since the azeotropic mixture can be distilled without preferential concentration of one of the components.

Compositions according to the invention have the advantage that they provide a range of solvents which have a greater solvent power than 1,1,2-trichloro-l,2,-trifluoroethane while still retaining to a great extent the inertness of 1,1,2-trichloro-1,2,2-trifluoroethane to synthetic organic Patented Jan. 29., 1974 polymers, plastics, resins, resin laminates, resin-bonded paper board, Bakelite, fibreglass and like materials.

Because of this enhanced solvent power the use of time-consuming, costly and sometimes unacceptable mechanical devices, such as hand-scrubbing or Wiping which may cause damage to sensitive articles, may be avo ded.

The azeotropic mixture may be used in most of the normal applications of 1,1,2-trichloro-1,2,2-trifluoroethane provided that the increased solvent power of the azeotrope is not a hindrance to such an application. This increased solvent power may make it possible to shorten the cleaning cycles which are at present necessary with pure 1,1,2- trichloro-1,2,2-trifluoroethane and thus enable the capacity of existing plant to be increased.

The compositions of the invention may be used in conventional apparatus and employing conventional operating techniques. The solvent may be used without heat if desired, but the cleaning action of the solvent may be assisted by conventional means, for example use of boiling solvent, agitation or adjuvants.

In some applications it is advantageous to use ultrasonic irradiation in combination with the solvents. This is particularly true when removing certain tenacious fluxes from soldered joints, the ultrasonic irradiation helping to remove the solid and insoluble constituents of the flux.

The high stability of the solvent composition of the invention, and particularly of the azeotrope, under operating conditions makes it usually unnecessary to use stabilizers in the solvents. This has the advantage that when the solvent composition evaporates it leaves a perfectly clean surface uncontaminated with higher boiling stabilizers. However, it is possible that stabilizers may be necessary under corrosive conditions for example those in which the solvent comes into contact with oxidizing agents which can attack the components of the composition.

Other solvents or additives may be added to the solvent composition of the invention if it is desired to modify their cleaning or solvent power. Suitable additives include cationic, anionic and non-ionic detergents. Water may also be added in some circumstances, particularly when the compositions include a detergent, but this is not essential.

Solvent compositions according to our invention, and particularly the azeotrope, are useful in a wide range of applications, including removal of soldering fluxes from electrical equipment, in particular from equipment in which the composition is likely to come into contact with materials such as plastics or resins and cleaning of photographic film or magnetic recording tapes.

The invention is illustrated in the following examples in which all percentages are by weight:

Example 1 Pure 1,l,Z-trichloro-1,2,2-trifluoroethane was mixed with nitromethane and the mixture distilled through a vacuum jacketed column at high reflux ratio to obtain a constant boiling mixture. A small quantity of isopropanol was added whereupon it Was observed that the condensation and boiling temperatures reached a mimium. The difference between these temperatures also reached a minimum at this point. The composition of the liquid in the ebulliometer was then close to that of a ternary azeotrope. The azeotropic composition was defined more precisely by careful fractionation of a liquid of roughly azeotropic composition followed by analysis of the condensate by gas chromatography. The boiling point of the azeotrope was found by distilling it in a diflerential ebulliometer and measuring the condensation temperature relative to that of pure l,1,Z-trichloro-l,2,-trifluoroethane using an ebullioscopic Beckman thermometer.

The azeotrope was found to have a composition of about 95.5% of 1,1,2 trichloro 1,2,2-trifluoroethane,

"ice

3 about 95.5% of 1,1,2 trichloro 1,2,2 trifluoroethane, and a boiling point at 760 mm. Hg of 45.87 C.

The azeotrope was also found to be nonflammable by the Pensky-Martens closed cup test.

Example 2 The azeotropic mixture of Example 1 was tested for its effectiveness in removing a soldering flux from resinbonded printed circuit boards. A section of board was painted with a commercially-available flux sold under the trade name Multicore P025. The board was dried under infra-red heating for 2 minutes and then touch-soldered for 5 seconds with solder maintained at 250 C. The board was then immersed in boiling solvent for 1 minute, after which time it was removed and found to be free from all flux residues. For the purposes of comparison a section of board was similarly treated and immersed in Arklone L, a commercially-available solvent used for circuit-board cleaning, which is an azeotropic mixture comprising 97% of 1,l,2-trichloro-1,2,2-trifluoroethane and 3% of isopropanol. Extensive flux residues still remained on the board after removal from this solvent.

We claim:

1. An azeotropic composition consisting essentially of about 95.5% by weight of 1,1,2-trichloro-1,2,2-trifluoroethane, about 2.5% by weight of isopropanol and about 2% by weight of nitromethane and having a boiling point of about 46 C. at 760 millimeters of mercury pressure.

2. A method of cleaning an article comprising contacting the article with the azeotropic composition of claim 1.

3. A method according to claim 2 in which the article is a printed circuit board contaminated with soldering flux.

References Cited UNITED STATES PATENTS Barton et al. 252--171 WILLIAM E. SCHULZ, Primary Examiner US. Cl. X.R.

25267, Digest 9; 260-652.5

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3903009 *16 Nov 19732 Sep 1975Du PontAzeotrope of 1,1,2-trichloro-1,2,2-trifluoroethane, ethanol and nitromethane
US3960746 *25 Jul 19741 Jun 1976E. I. Du Pont De Nemours And CompanyAzeotrope-like compositions of methanol, nitromethane and trichlorotrifluoroethane
US4045366 *16 Nov 197630 Aug 1977Allied Chemical CorporationAzeotrope-like compositions of trichlorotrifluoroethane, nitromethane and acetone
US4052328 *16 Nov 19764 Oct 1977Allied Chemical CorporationAzeotrope-like compositions of trichlorotrifluoroethane, ethanol, isopropanol and nitromethane
US4062794 *16 Nov 197613 Dec 1977Allied Chemical CorporationAzeotrope-like compositions of trichlorotrifluoroethane, methanol, ethanol, isopropanol and nitromethane
US4279664 *9 Apr 198021 Jul 1981Allied Chemical CorporationAzeotrope-like compositions of trichlorotrifluoroethane, acetone and n-hexane
US4279665 *9 Apr 198021 Jul 1981Allied Chemical CorporationAzeotrope-like compositions of trichlorotrifluoroethane, acetone and cyclopentane
US4584122 *28 Nov 198422 Apr 1986Allied CorporationAzeotrope-like compositions of trichlorotrifluoroethane, ethanol, nitromethane and 2-methylpentane or a mixture of hexanes
US4593764 *8 Nov 198410 Jun 1986Conoco Inc.Removal of pipe dope constrictions
US4606841 *28 Nov 198419 Aug 1986Allied CorporationAzeotrope-like compositions of trichlorotrifluoroethane, ethanol, acetone, nitromethane and hexane
US4715900 *8 Jan 198729 Dec 1987E. I. Du Pont De Nemours And CompanyAzeotropic compositions of trichlorotrifluoroethane, dichlorodifluoroethane and methanol/ethanol
US4753735 *27 Oct 198628 Jun 1988Allied-Signal Inc.Solvent and apparatus and method for cleaning and drying surfaces of non absorbent articles
US4873021 *30 Dec 198610 Oct 1989E. I. Du Pont De Nemours And CompanyAzeotrope or azeotrope-like composition of trichlorotrifluoroethane and dichlorodifluoroethane
US4936923 *1 Mar 198926 Jun 1990E. I. Du Pont De Nemours And CompanyAzeotropic compositions of 1,1,2-trichlorotrifluoroethane with cis-1,2-dichloroethylene and n-propanol or isopropanol with or without nitromethane
US5035831 *6 Oct 198930 Jul 1991Allied-Signal Inc.Azeotrope-like compositions of 1,1,2-trichloro-1,2,2-trifluoroethane, nitromethane, 1,2-dichloroethylene, and ethanol or isopropanol
US5073288 *17 Aug 199017 Dec 1991E. I. Du Pont De Nemours And CompanyCompositions of 1,1,1,2,2,3,5,5,5-nonafluoro-4-trifluoromethylpentane and use thereof for cleaning solid surfaces
US5073290 *17 Aug 199017 Dec 1991E. I. Du Pont De Nemours And CompanyCompositions of 1,1,1,2,2,5,5,5-octafluoro-4-trifluormethypentane and use thereof for cleaning solid surfaces
US5076956 *29 Nov 199031 Dec 1991E. I. Du Pont De Nemours And CompanyCompositions of octafluorotrifluoromethylpentane and nonafluorotrifluoromethylpentane and use thereof for cleaning solid surfaces
US5084199 *9 Oct 199028 Jan 1992E. I. Du Pont De Nemours And Company1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US5171902 *11 Oct 199015 Dec 1992E. I. Du Pont De Nemours And CompanySaturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
US5176757 *28 Oct 19915 Jan 1993E. I. Du Pont De Nemours And Company1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US5221361 *4 Sep 199122 Jun 1993E. I. Du Pont De Nemours And CompanyCompositions of 1,1,1,2,2,5,5,5,-octafluoro-4-trifluoromethylpentane and use thereof for cleaning solid surfaces
US5250213 *6 May 19915 Oct 1993E. I. Du Pont De Nemours And Company1,1,1,2,2,3,3,4,4,5,6-undecafluorohexane and use thereof in compositions and processes for cleaning
US5268122 *28 Aug 19917 Dec 1993E. I. Du Pont De Nemours And CompanyGem-dihydropolyfluoroalkanes and monohydropolyfluoroalkenes, processes for their production, and use of gem-dihydropolyfluoroalkanes in cleaning compositions
US5504265 *27 Jul 19922 Apr 1996E. I. Du Pont De Nemours And CompanySaturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
US5683978 *2 Jun 19954 Nov 1997E. I. Du Pont De Nemours And CompanySaturated linear polyfluorohydrocarbons in cleaning compositions
US5723701 *2 Jun 19953 Mar 1998E. I. Du Pont De Nemours And CompanySaturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
US619461910 Sep 199327 Feb 2001E. I. Du Pont De Nemours And CompanyGem-dihydropolyfluoroalkanes and monohydropolyfluoroalkenes, processes for their production, and use of gem-dihydropolyfluoroalkanes in cleaning compositions
US65069502 Jun 199514 Jan 2003E. I. Du Pont De Nemours And CompanySaturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
DE2533357A1 *25 Jul 19755 Feb 1976Du PontAzeotropartige stoffzusammensetzung
Classifications
U.S. Classification510/178, 252/67, 570/110, 510/409
International ClassificationC11D7/50
Cooperative ClassificationC11D7/5095
European ClassificationC11D7/50D4K