US3692686A

US3692686A - Novel non-flammable azeotrope solvent composition

Info

Publication number: US3692686A
Application number: US77388A
Authority: US
Inventors: Oliver A Barton; Kevin P Murphy
Original assignee: Allied Chemical Corp
Current assignee: Allied Corp
Priority date: 1970-10-01
Filing date: 1970-10-01
Publication date: 1972-09-19
Anticipated expiration: 1989-09-19
Also published as: US3836474A

Abstract

TETRACHLORODIFLUOROETHANE (SYM.-, ASYM.-, AND MIXTURES THEREOF) NITROMETHANE, WATER AND ISOPROPANOL OR SECONDARY BUTANOL FORM QUATERNARY AZEOTROPIC MIXTURES WHICH ARE USEFUL AS DRY CLEANING SOLVENTS AND ARE PARTICULARLY USEFUL FOR THE REMOVAL OF HARD-TO-REMOVE STAINS FROM LEATHER.

Description

United States Patent Office Patented Sept. 19, 1972 3,692,686 NOVEL NON-FLAMMABLE AZEOTROPE SOLVENT COMPOSITION Oliver A. Barton, Florham Park, N.J., and Kevin P. Murphy, Orchard Park, N.Y., assignors to Allied Chemical Corporation, New York, N.Y. No Drawing. Filed Oct. 1, 1970, Ser. No. 77,388 Int. Cl. C09d 9/00; Clld 7/50; C23g /02 US. Cl. 252171 10 Claims ABSTRACT OF THE DISCLOSURE Tetrachlorodifluoroethanc (sym.-, asym.-, and mixtures thereof) nitromethane, water and isopropanol or secondary butanol form quaternary azeotropic mixtures which are useful as dry cleaning solvents and are particularly useful for the removal of hard-to-remove stains from leather.

BACKGROUND OF THE INVENTION In conventional dry cleaning processes for the removal of dirt, grease and various soils from textile and leather articles, use is made of organic solvents having dissolved therein a detergent in minor amounts. The dry-cleaning bath may also contain other additives such as water, textile softeners, water repellents and the like.

Solvents commonly used as the organic components of such dry cleaning compositions include saturated aliphatic hydrocarbons such as Stoddard solvent, gasoline or other low boiling paraffinic hydrocarbons; low-boiling aromatic hydrocarbons, such as benzene, toluene, and xylene; and low-boiling polyhalogenated hydrocarbons of l to 2 carbon atoms such as carbon tetrachloride, methyl chloroform, trichloroethylene, tetrachloroethylene, trichlorofluoromethane, dichlorotrifluoroethane, trichlorodifluoroeth ane, and mixtures of these.

Numerous anionic, cationic, and nonionic detergents have been used as additives to the dry cleaning compositions. Such additives, are known to have adverse effects when contacted with leather articles in that they remove the natural oil or grease from the leather leaving it harsh and brittle.

Other candidate solvent compositions, although having satisfactory solvency characteristics, are flammable and/ or toxic, thereby creating hazards to personnel in their use. In addition, because of the diverse character of the many stains and solids encountered and the many different types of textiles, both natural and synthetic, which are encountered by dry cleaning establishments, much dry cleaning must practically be carried out on a custom basis and requires hand spotting to remove deep stains.

The stains encountered in the dry cleaning process can be broadly categorized as organic solvent-soluble and water-soluble. Thus, grease and oil stains can be effectively removed by organic solvents such as perchloroethylene, while catsup, perspiration, common dirt stains and the like are removed by water. Since both types of stains or soils are usually present on garments and the like submitted for dry cleaning, it would be desirable to include both organic solvents and water in the dry cleaning liquor. Since water and the common dry cleaning solvents are not mutually soluble to any useful extent, it is general practice in this art, as noted above, to utilize emulsifying agents, such as alkylaryl sulfonates, to increase the water tolerance of the organic solvents. To obtain an effective increase in the water tolerance of many dry cleaning solvents requires the use of relatively large proportions of emulsifying agent. This not only increases the cost of the solvent mixture but also such large proportions of emulsifying agent adversely affect the material being cleaned,

for example, by removing natural oils, sizing agents, water proofing resins, and the like. Moreover, many textile materials are sensitive to excessive moisture. Wool, for example, may shrink, and rayon and certain synthetics may wrinkle when cleaned with solvents containing excessive moisture. A delicate balance between organic solvents and water must be maintained.

It is common practice to use polyhalogenated lower alkanes such as trichlorotrifluoroethane, tetrachlorodifluoroethane, and the like, for solvent cleaning of a variety of materials. Such compounds are notably of low toxicity for warm blooded animals and are non-flammable. However, such solvents are not entirely for use in dry cleaning of textile materials since no known single compound is an effective solvent for the wide variety of stains encountered.

A variety of solvent mixtures have been tested for such purposes but generally have been found to be lacking to a greater or lesser extent in one or more of the desired characteristics of dry cleaning mixtures. Such mixtures may contain two or more halocarbons or at least one halocarbon together with another organic compound such as an alcohol, ether, or ketone. In the usual instance, such mixtures are not constant boiling, that is they fraction-ate during use and during reclamation, losing one or more of the more volatile components. Such mixtures with altered compositions may have less desirable properties such as lower solvency for stains, less inertness towards textile materials and increased flammability.

A number of azeotropic mixtures have been suggested for cleaning of a variety of materials. Azeotropes do not suffer from the above discussed fractionation disadvantage possessed by non-constant boiling mixtures. Unfortunately, the solvency character of the known azeotropic compositions leave much to be desired when employed in the cry cleaning of most textile materials and, particularly, leather articles. Such compositions have very low tolerance for water and hence, while eifective to remove oil-soluble stains, are efiective to remove water-soluble stains.

Moreover, although azeotropic compositions possess the above described advantages over non-azeotropic (non-constant boiling) compositions, as evidenced by the disclosure in US. Pat. 3,085,065 to Kvalnes, a basis has not been found for predicting the formation of azeotropes between or among halocarbons, much less mixtures of halocarbons and other organic compounds and/ or water.

It is, therefore, a major object of this invention to provide novel solvent compositions for removing stains normally encountered on textile materials and leather which novel solvent compositions exhibit a high degree of solvency for such stains.

Another object of this invention is to provide novel solvent compositions which are constant boiling or essentially constant boiling.

Still another object is to provide novel solvent compositions containing an organic solvent and water which exhibit high solvency toward both oil-soluble and watersoluble stains.

SUMMARY OF INVENTION In accordance with the present invention, we have discovered constant boiling mixtures which are highly effective dry cleaning solvents for removing common household stains, and which do not include a detergent compound. The novel constant boiling mixtures of our invention consist essentially of tetrachlorodifluoroethane, nitromethane, water and isopropanol or secondary butanol.

More particularly our invention includes the novel azeotropic mixtures consisting essentially of about 76.8 weight percent of tetrachlorodifluoroethane, about 9.3 weight percent of nitromethane, about 3.7 weight percent of Water,

and about 10.2 weight percent of isopropanol. These quaternary azeotropic mixtures of the invention boil at about 69.0 C. at 760 mm. pressure.

The invention also includes the novel azeotropic mixtures consisting essentially of about 78.6 weight percent of tetrachlorodifluoroethane, about 14.1 weight percent of nitromethane, about 4.7 weight percent of water, and about 2.6 weight percent of secondary butanol. These quaternary azeotropic mixtures of this invention boil at about 70.5 C. at 760 mm. pressure.

These novel solvent mixtures are constant boiling or essentially constant boiling and thus can be recovered after use by distillation without change in composition or solvent properties.

The novel solvent mixtures have been found to be effective cleaning compositions for leather and in use are contracted with the soiled leather for a period of time sufiicient to effect substantially complete dissolution of the oil-soluble and water-soluble stains, such as catsup, can be removed without noticeably reducing the flexibility or softness (hand) of the leather article.

The novel quaternary solvent mixtures of the invention on standing, separate into two layers. However we have found that the separated mixtures can be readily dispersed to uniform emulsions by gentle agitation and without recourse to emulsifying agents.

The lower layers which separate from the quaternary mixtures on standing are highly effective dry cleaning solvents for textile materials such as wool and in use are contacted with the soiled textile materials for a period of time sufiicient to effect substantially complete dissolution of the oil-soluble and water-soluble stains. These lower layers contain only a minimum concentration of water and hence while effective for the removal of water-soluble stains, do not cause shrinkage of wool or wrinkling of rayon.

The lower layer obtained from the isopropanol containing azeotropes has the approximate composition of Percent Tetrachlorodifluoroethane 80.00 Isopropanol 9.7 Nitromethane 9.3 Water 1.0

This layer amounts to about 96% of the original quaternary azeotropic mixture.

The upper layer contains substantially none of the tetrachlorodifluoroethane. This layer contains about Percent Water 69.0

Isopropanol 22.2 Nitromethane 8.8

Percent Tetrachlorodifluoroethane 89.36 Sec.-butanol 2.0 Nitromethane 8 .6

Water 0.04

This layer amounts to about 95% of the original quaternary azeotropic mixture.

The upper layer contains substantially none of the tetrachlorodifluoroethane. This layer contains about Percent Water 82.2 Sec.-butanol 4.6 Nitromethane 13.2

This layer, which amounts to less than 5% of the azeotrope, may likewise be drawn off and either discarded or admixed with additional tetrachlorodifluoroethane and the mixture distilled to recover an additional quantity of the quaternary azeotrope.

The halocarbon component of the novel quaternary mixtures of the invention is available commercially as a mixture of about 69 mol percent of the symmetrical isomer, 1,1,2,2 tetrachloro-Z,2-difluoroethane and about 31 mol percent of the asymmetrical isomer, l,1,l,2-tetrachloro-2, Z-difluoroethane. We have found that either isomer, per se, or the commercially available mixtures thereof, when admixed with nitromethane, secondary butanol or isopropanol and water, yield azeotropic mixtures of substantially identical characteristics and properties. Accordingly, all references contained in this specification to tetrachlorodifiuoroethane apply to mixtures of the two isomers, in any proportions, or to either isomer, per se.

The following examples will illustrate the invention. Unless otherwise indicated, parts and percentages are by weight and temperaturesare given in degrees centigrade.

EXAMPLE 1 Preparation of the quaternary azeotrope Percent Tetrachlorodifluoroethane 76.8 Isopropanol 10.2 Nitromethane 9.3 Water 3.7

On standing, the fraction separated into two layers. The lower layer, which constituted 96.0% of the total fraction, was analyzed by gas liquid chromatography and was found to possess the following composition Percent Tetrachlorodifluoroethane 80.0 Isopropanol 9.7 Nitromethane 9.3 Water 1.0

(b) Repetition of the procedure set out in part (a), but substituting an equivalent amount of pure (97 mole percent) 1,1,2,2-tetrach1oro-1,2-difluoroethane for the commercially available mixture of isomers gave a quaternary azeotrope boiling at 69.1 and 760 mm. pressure and having essentially the same composition as that mixture obtained by using the commercial mixture of tetrachlorodifluoroethane isomers.

(c) Repetition of the procedure set out in part (a), above, but substituting an equivalent amount of 1,1,l,2 tetrachloro-2,2-difluoroethane for the commercial mixture of isomers gave a quaternary azeotrope boiling at 686 at 760 mm. pressure and having essentially the same composition.

These results indicate that azeotropic mixtures in accordance with our invention can be obtained using either pure isomers of tetrachlorodifluoroethane or any mixture thereof. Such azeotropes possess substantially iden tical compositions and have no significant difference in properties.

EXAMPLE 2 Preparation of quaternary azeotrope (a) Equimolecular quantities of tetrachlorodifluoroethane (B.P. 92.8"), the commercially available mixture,

Percent Tetrachlorodifluoroethane 78.6 Sec.-butano1 2.6 Nitromethane 14.1 Water 4.7

On standing, the fraction separated into two layers. The lower layer, which constituted 95.3% of the total fraction, was analyzed by gas liquid chromatography and was found to possess the following composition:

Percent Tetrachlorodifluoroethane 89.36 Sec.-butanol 2.0 Nitromethane 8.6 Water 0.04

(b) Repetition of the procedure set out in part (a), but substituting an equivalent amount of pure (97 mole percent), 1,1,2,2-tetrachloro-1,2-difiuoroethane for the commercially available mixture of isomers gave a quaternary azeotrope boiling at 70.3" at 760 mm. pressure and having essentially the same composition as that mixture obtained by using the commercial mixture of tetrachlorodifiuoroethane isomers.

(c) Repetition of the procedure set out in part (a), above, but substituting an equivalent amount of 1,l,1,2- tetrachloro-2,2-difiuoroethane for the commercial mixture of isomers gave a quaternary azeotrope boiling at 70.7 at 760 mm. pressure and having essentially the same composition.

These results indicate that azetropic mixtures in accordance with our invention can be obtained using either pure isomers of tetrachlorodifluoroethane or any mixture thereof. Such azeotropes possess substantially identical compositions and have no significant difference in properties.

EXAMPLE 3 Use of the quaternary azeotrope as a dry cleaning solvent for leather Swatches of natural (undyed) sheepskin suede leather, 2 in. x 8 in., were soiled with one of the following: lip stick, catsup, grape juice or lanolin. The stains were allowed to dry and to set for 24 hours at ambient temperature. The stained swatches were then cleaned in an agitated bath containing about 350 cc. of a particular test cleaning solvent.

The cleaning cycle was carried out for /2 hour and at ambient temperature.

The test solvents used were the azeotrope prepared in Example 1, part (a) above, the respective components of the azeotrope, and perchloroethylene, a well known, commercially available dry cleaning solvent.

The results of these tests are set out in tabular form in Table 1 below. The effectiveness of the stain removal was rated by visual observation on a scale of 1 to with 1 being substantially no stain removal and 10 being complete removal of the stain.

These results indicate the general overall effectiveness of the azeotrope composition as a soil remover from suede leather. Other solvents tested, while as good for removal of a particular soil, are ineffective with respect to removal of one or more of the other stains tested.

The data set out in Table 1 indicate the presence of synergism in the quaternary mixture of the invention. The numerical ratings are approximations of the percentage removal of the several stains, that is a rating of 5 is equivalent to about 50% removal of the stain. These percentages multiplied by the concentration of the particular solvent in the quaternary mixture give a quantitative indication of the amount of the stain which would be expected to be removed by the solvent in the mixture. The sum of these results in each instance is less than the analogous value (ratingXlO) actually obtained with the quaternary mixture.

Thus a quantitative summation of the removal of lipstick stain by each of the four component solvents totals 61.5% whereas the quaternary mixture removed 100% of the stain.

The total grape juice removed would be expected to be 60.57%. Actually 100% of this stain was removed by the azeotrope.

The total catsup removed would be expected to be 39.74%. Actually, 100% of the stain was removed.

The total lanolin removed would be expected to be 96.7%. Actually 100% of the lanolin was removed by the quaternary azeotrope.

Accordingly, based on this method of calculation, the novel quaternary azeotrope of the invention exhibits a synergistic effect in the removal of both oil-soluble and water-soluble stains from leather.

EXAMPLE 4 Use of the quaternary azeotrope containing sec.butanol as a dry cleaning solvent for leather In an analogous manner to that described in Example 3 above, the quaternary azeotrope containing secondary butanol prepared in Example 2, part (a) above, was tested as a dry cleaning solvent for soiled suede leather. In this instance Stoddard solvent, a well-known commercially available dry cleaning solvent, was used in place of perchloroethylene as a standard.

The results of these tests are set out in Table II below.

These results indicate the general overall eifectiveness of the azeotrope composition as a soil remover from suede leather. Other solvents tested, while as good or slightly superior from removal of a particular soil, are inelfective with respect to removal of one or more of the other stains tested. Using the method of calculation described in Example 3 above the data of Table II can likewise be used to indicate the presence of synergism in the azeotropic mixture tested in this example.

Thus a quantitative summation of the removal of lipstick stain by each of the four component solvents totals 56.4% whereas the quaternary mixture removed 100% of the stain.

The total grape juice removed would be expected to be 51.4%. Actually, of this stain was removed by the azeotrope.

The total catsup removed would be expected to be 35.34%. Actually, 90% of the stain was removed.

The total lanolin removed would be expected to be 93.2%. Actually of the lanolin was removed by the quaternary azeotrope.

EXAMPLE Dry cleaning of water sensitive textiles with lower layer of azeotrope Certain te'xtile materials, such as wool are sensitive to excessive moisture in dry cleaning solvents. Such sensitivity is evidenced by shrinkage. Some moisture is desirable, however, for etfective cleaning.

As has been indicated, the quaternary azeotropes on standing, separate into two phases, the lower of which contains only a minimum quantity of water. This amount, in the presence of the organic solvents does not cause shrinkage and/or wrinkling of textiles during the cleaning of said textiles. The avoidance of shrinkage serves to preserve the original character of the cleaned textile. The absence of wrinkles reduces or eliminates the need for pressing of the cleaned textile.

This property of the lower phase of the azeotrope is shown by the following comparative test wherein the etfect of this mixture of solvents on wool and rayon textile material was compared with a standard dry cleaning composition. The standard consisted of perchloroethylene containing 1% of water and 1% of Aerosol 0T (a synthetic detergent consisting essentially of the sodium salt of dioctylsulfosuccinic acid).

In this test, measured swatches of the particular textile material were immersed in an agitated bath of the dry cleaning solvent composition for /2 hour at ambient temperature. After removal from the bath. the swatches were dried and remeasured for shrinkage. The samples, after cleaning, were checked for the presence of wrinkles.

The results of these tests are recorded in Table HI below:

1 Average shrinkage of 2 Perchloroethylene containing 1% water and 1% Aerosol OT.

The used lower layer solvent mixture can be readily recovered by passing the solvent through a filter to remove solid particles. To the filtrate a mixture of about 4% water, 0.3% sec.-butanol and 0.8% nitromethane or a mixture of about 4% water, 0.88% isopropanol and 0.35% nitromethane is added and the mass is fed to a still. On distillation, a quaternary azeotrope of the same composition as that obtained in Example 2, part (a) above or Example 1, part (a), above is obtained. This is permitted to stratify and the lower layer is drawn oil to a suitable storage vessel to be recycled. The upper layer of the azeotrope can be preserved for use as build up for used solvent in this recovery process. The still bottoms, consisting essentially of water and dissolved soil, are discarded.

The novel solvent mixtures of the invention find other solvent applicants such as for removing gases, oils and inorganic salts from a variety of industrial items, for

cleaning of photographic films and prints, for removal of bufiing compounds, such as rouge, and also may be used as heat exchange media and as chemical reaction media.

'It will be apparent to those skilled in the art that, for specialized purposes, various additives could be ire corporated with the novel mixtures of the invention, for example lubricants, water proofing resins, moth proofing chemicals and the like. These additives are chosen and used in amounts so as not to adversely alfect the essential properties of the mixtures for a given purpose.

The invention is not intended to be limited by any specific embodiments disclosed herein, but only by the scope of the following claims.

We claim:

1. Constant boiling mixtures consisting essentially of about 76.8 weight percent of tetrachlorodifiuoroethane, about 10.2 weight percent of isopropanol, about 9.3 weight percent of nitromethane and about 3.7 weight percent of water, said mixtures boiling at about 70.5 C. at 760 mm.

2. Constant boiling mixtures as described in claim 1 in which the tetrachlorodifiuoroethane is a mixture of about 69 mol percent of 1,1,2,2-tetrachloro-1,2-difiuoroethane and about 31 mol percent of 1,1,1,2-tetrachloro- 2,2-difiuoroethane.

3. Constant boiling mixtures as described in claim 1 in which the tetrachlorodifiuoroethane is substantially pure 1,1,2,2-tetrachloro-1,2-difiuoroethane.

4. Constant boiling mixtures as described in claim 1 in which the tetrachlorodifiuoroethane is substantially pure 1,1, 1,2-tetrachloro-2,2-difluoroethane.

5. Constant boiling mixtures consisting essentially of about 78.6 weight percent of tetrachlorodifiuoroethane, about 2.6 weight percent of secondary butanol, about 14.1 weight percent of nitromethane and about 4.7 weight percent of Water, said mixtures boiling at about 70.5 C. at 760 mm.

6. Constant boiling mixtures as described in claim 5 in which the tetrachlorodifiuoroethane is a mixture of about 69 mol percent of 1,-1,2,2-tetrachloro-1,2-difluoroethane and about 31 mol percent of 1,1,1,2-tetrachloro-2,2-difluoroethane.

7. Constant boiling mixtures as described in claim 5 in which the tetrachlorodifiuoroethane is substantially pure 1,1,2,2-tetrachloro-1,2-difiuoroethane.

8. Constant boiling mixtures as described in claim 5 in which the tetrachlorodifiuoroethane is substantially pure 1, 1,1,2-tetrachloro-2,Z-difluoroethane.

9. The process of dry cleaning leather which comprises contacting for a period of time sufficient to efiect substantially complete dissolution of oil-soluble and Watersoluble stains, leather to be cleaned with a constant boiling mixture as described in claim 1, separating said leather from said constant boiling mixture and drying said leather.

10. The process of dry cleaning leather which comprises contacting for a period of time sufiicient to effect substantially complete dissolution of oil-soluble and water-soluble stains, leather to be cleaned with a constant boiling mixture as described in claim 5, separating said leather from said constant boiling mixture and drying said leather.

References Cited UNITED STATES PATENTS 3,285,858 11/1966 Hirsch et a1 252l71 3,085,116 4/ 1963 K valnes 260'652.'5 3,530,073 9/1970 Clark et al 252DIG. 9 3,042,479 7/ 1962 Hicks et a1. 8-142 L'EON D. ROSDOL, Primary Examiner W. E. SCHULZ, Assistant Examiner U.S. Cl. X.R.

8--142; 252DIG. 9; 260652.5