US2565403A - Textile oils - Google Patents

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US2565403A
US2565403A US23474A US2347448A US2565403A US 2565403 A US2565403 A US 2565403A US 23474 A US23474 A US 23474A US 2347448 A US2347448 A US 2347448A US 2565403 A US2565403 A US 2565403A
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oil
viscosity
textile
weight
scouring
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Lorne W Sproule
Thomas W Dixon
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Standard Oil Development Co
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Standard Oil Development Co
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions

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  • the present invention pertains to a textile oil and more particularly to an emulsifiable textile oil which affords efiective lubrication for weaving yarns and the like and which can be readily removed by ordinary scouring operations without injury to the textile material.
  • textile oils have commonly included fatty oils of vegetable or animal origin, for example olive oil which is a very satisfactory textile oil but is expensive and has a tendency to become rancid in use.
  • mineral oils on textiles i well known but these have not been particularly satisfactory for various reasons and especially because they are difficult to wash or scour out of the finished fabric.
  • Another Way of stating this quantitatively is to state that the residual oil should not be more than a small fraction, for example a maximum of 10 or 15% of the original quantity of oil used on the yarn.
  • a mineral oil mixed with a suitable emulsifying agent might be diluted or emulsified with water so as to minimize the quantity of lubricant required and to obtain more even distribution of the oil on the wool and also to facilitate its removal.
  • a textile oil which consists of a suitable mineral oil, preferably a white mineral oil, containing about 7% by weight of an oil soluble sulfonate and a small quantity of an ester, such as triethanolamine oleate.
  • the patent referred to describes various compositions wherein the quantities of sulfcnates, esters, etc., may be varied somewhat and it suggests also the use of a sulfonated lard oil as a principal additive to the mineral oil.
  • a sulfonated lard oil as a principal additive to the mineral oil.
  • the present invention is an improvement over the invention described in said patent to Holtzclaw and Winning.
  • a particularly desirable lubricating composition may be made of mineral oil of appropriate grade, a suitable oil soluble sulfonate in proper proportions, and small controlled quantities of specific wetting or surface active agents which render the lubricants readily emulsifiable in water.
  • the type of emulsifying agent used according to this invention does not have the objectionable property of unduly raising the viscosity of solutions of sodium sulfonates in mineral oil. Hence, textile oils containing large amounts of sulfonates, with the corresponding improvement in securing properties, can be utilized.
  • Textile oils prepared by dissolving large amounts (18 to 25%) of sodium sulfonate concentrate (65/35) in mineral oil can be scoured from fabric very satisfactorily. Such materials, however. do not form readily emulsifiable oils and it is necessary to add a third component to produce the required emulsibility. When this is done in accordance with the Holtzclaw and Winning patent, the viscosity of the resulting material is too high for textile processing.
  • a textile oil is prepared by dissolving 18 to 25% sodium sulionate concentrate (65/35) and made readily emulsifiable by the addition of 0.5 to 1.5% of the polyoxyethylene derivative of sorbitan mono-oleate, then its viscosity is not as high, and, furthermore, can be adjusted readily by the addition of small amounts of sorbitan mono-oleate and/or ethylene glycol monobutyl ether. It is desirable that the viscosity should be between about 100 and 300 S. S. U. at 100 F.
  • the following method is used in determining the quantity of oil which is removed in conven tional scouring.
  • the scouring solution consists of water containing 0.2% by weight of soap,
  • soda soaps of low titre and 0.1% of soda ash It is maintained at a temperature of 110 F.
  • the jar is placed in a frame and rotated about its horizontal axis at, 50 R. P. M. for. a period of twenty minutes. After scouring, the sample is rinsed in water at about room temperature, dried, and the residual oil content determined by ether extraction. The residual oil content is expressed as the percentage of original oil applied.
  • a light mineral oil for example one having a viscosity of 100 S. S. U. at 100 F. and a viscosity index of 95 attains a viscosity of 1'77 S. S. U. at 100 F. when 12% of a sodium sulfonate concentrate (65% sulfonate in mineral oil) is added.
  • the actual sulfonate content in this case is approximately 8% by weight and the sulfonate has a molecular weight of about 460.
  • woolen fabrics, lubricated with 10% by weight of such an oil are subjected to the securing test described above, 25% of the oil remains in the fabric as determined by extraction of the oil with ether.
  • composition was prepared by mixing together at ordinary temperatures 86.7% by weight of a mineral oil having a viscosity of S. S. U. at 100 F. and a viscosity index of 95, 12% by weight of sodium sulfonate concentrate (actually about 8% of sulfonate in the final product), 1% sorbitan monooleate polyoxyalkylene derivative, and 0.3% of sorbitan mono-oleate.
  • This composition had a viscosity of 184 S. S. U. at 100 F., remained stable for 24 hours in a 10% emulsion and showed 23.9% residual oil after scouring with a standard scouring solution containing 0.2% of standard textile soap and 0.1% soda ash when tested in accordance with the procedure previously described.
  • EXAMPLE III A composition consisting of 80.5% of the same mineral oil as described above in Example II, 18.0% of sodium sulfonate concentrate as above (i. e. about 12% sodium sulfonate having average molecular weight of about 460) 1.0% of the sorbitan mono-oleate polyoxyalkylene derivative, and 0.5% of sorbitan mono-oleate.
  • This composition has a viscosity of 202 S. S. U. at 100 F., passed the 24 hour emulsion stability test for a 10% emulsion and showed only 9.5% residual oil after scouring.
  • EXAMPLE IV This composition was precisely the same as that of Example 111 except that only one wetting agent was employed, that is 1.5% of sorbitan monooleate polyoxyetliylene derivative. It passed the emulsion test mentioned above satisfactorily, showed a residual content after scouring of only 9.2% of the original oil used, but its viscosity was higher, 244 S. S. U. at 100 F.
  • EXAMPLE v A composition was prepared containing 73.5% of the mineral oil described above, together with 25% of the sodium sulfonate concentrate, 1.0% of sorbitan mono-oleate polyoxyethylene derivative and 0.5% of sorbitan mono-oleate. It passed the emulsion test and showed a residual oil content of only 4.1% but its viscosity was 302 S. S. U. at 100 F., too high for general use.
  • Sorbitan mono-oleate-polyoxyethylene derivative 1.0 1.0 1 5 1.0 1.0 Sorbitan mono-oleate 0.3 0.5 0.6 0.5 Butyl Cellosolve (Ethylene glycol nonobutyl ether) 1. Mineral Oil (V./100--100 F., V.
  • Formula er cent (1 w'efiht Sodium Sulionate Concentrate (65/35).
  • Mineral Oil 100 S. S. U. at 100 F., 35 V.
  • I Mineral Oil 100 S. S. U. at 100 F.,
  • the lubricant used had the following composition:
  • the wool wa's oiled with 6% by weight of the oil based on the weight of the wool in the form of a 30% aqueous emulsion.
  • the wool was then subjected to the various processing operations. encountered in the manufacture of woolen cloth such as carding, spinning and weaving.
  • the oil in the cloth was then removed using a scour consisting of 0.14% of soap and 0.28% soda ash.
  • the invention contemplates the use of various quantities of sulfonates and other wetting on emulsifying agents with or without the use of a small quantity of organic solvent to reduce the over-all viscosity of the composition when such viscosity exceeds desirable limits.
  • a light mineral oil or mineral base oil for example an oil of 50 to 200 S. S. U. viscosity at 100 F., preferably having a viscosity between about 75 and S. S. U. at 100 F. This oil will comprise about 70 to. 94.5% by weight of the total composition.
  • a metal sulfonate preferably an oil soluble alkali metal sulfonate.
  • the sulfonate is normally added as a concentrate in mineral oil. For example 18% of a 65/35 mineral oil solution of sodium sulfonate is equivalent to 11.7% concentration of the pure sulfonate. Proportions of the concentrate added will range from about 7 to 80%.
  • the percentage figures used in the accompanying claims refer to the pure sulionate or to a substantially pure compound, it being understood that the useful oil soluble sulionates also may be mixtures of the salts of various metals 1! desired.
  • emulsifying agents While reference has been made above to specific emulsifying agents, it will be understood that various synthetic emulsifying agents may be employed, although the fatty acid esters, and particularly the fatty acid mono-esters of polyhydric alcohols, are preferred. In particular, the fatty acid mono-ester of hexahydric alcohols are preferred, the esters of sorbitan (partially dehydrated sorbitol) being especially suitable.
  • organic solvents may be used in proportions from about 0.1 to about 3.0%, based on the total composition, to control viscosity.
  • the use of such solvents is advantageous when high concentrations of sulfonates are employed.
  • the invention contemplates the use of from 5 to of dry sulfonate (i. e., aside from mineral oil solvent), 0. 5 3% of synthetic emulsifying agent and 0 to 3% of the solvent.
  • butyl Cellosolve ethylene glycol mono-butyl ether
  • other solvents may be used, the mono-alkyi ethers of ethylene glycol (known commercially as the Cellosolve compositions) being particularly preferred.
  • the overall mineral oil content will therefore range between about 77 and 94.5% by weight.
  • a textile oil composition of low viscosity and good scouring characteristics consisting essentially of 76 to 94.4% by weight of mineral oil oi 50 to 200 S. S. U. viscosity at 100 F., 5 to 20% of oil soluble alkali metal sulfonate having a molecular weight between 380 and 480, 0.5 to 2.5% of the polyoxyethylene derivative of sorbitan mono-oleate, and 0.1 to 1.5% of sorbitan monooleate.
  • a textile oil composition consisting essen tially of mineral oil of about 100 s. S. U. viscosity at 100 P. which contains about 6.3% by weight, based on the total composition, of sodium sulfonate having a molecular weight between 380 and 480, 1.0% of the polyoxyethylene derivative of 'sorbitan mono-oleate and 0.5% of sorbitan mono-oleate;
  • composition according to claim 2 to which is added 0.1 to 3.0% by weight of a glycol monoether to reduce viscosity.

Description

Aug. 21, 1951 L. w. SPROULE ET AL TEXTILE OILS Filed April 27', 1 948 o 6 o o 0 O O 0 O O O 0 0 O O 6 4 2 O 5 6 4 2 0 6 6 5 v5 5 5 4 4 4 4 4 3 5 IN FAbRlC. (bAsED ON WEIGHT OF OIL- APPLIED) QESIDUAL. OIL. LEFT Patented Aug. 21, 1951 UNITED STATES PATENT OFFICE TEXTILE OILS Lorne W. Sproule and Thomas W. Dixon, Sarnia,
Ontario, Canada, assignors to Standard Oil Development Company, a corporation of Delaware Application April 27, 1948, Serial No. 23,474
4 Claims. 1
The present invention pertains to a textile oil and more particularly to an emulsifiable textile oil which affords efiective lubrication for weaving yarns and the like and which can be readily removed by ordinary scouring operations without injury to the textile material.
In the prior art, textile oils have commonly included fatty oils of vegetable or animal origin, for example olive oil which is a very satisfactory textile oil but is expensive and has a tendency to become rancid in use. The use of mineral oils on textiles i well known but these have not been particularly satisfactory for various reasons and especially because they are difficult to wash or scour out of the finished fabric. Ordinarily, it is desirable that the residual oil which remains in a textile material after scouring with soap and soda ash, for example, should not exceed about 0.5% by weight, based on the total weight of the finished textile. Another Way of stating this quantitatively is to state that the residual oil should not be more than a small fraction, for example a maximum of 10 or 15% of the original quantity of oil used on the yarn.
It has previously been suggested that a mineral oil mixed with a suitable emulsifying agent might be diluted or emulsified with water so as to minimize the quantity of lubricant required and to obtain more even distribution of the oil on the wool and also to facilitate its removal. For example, in Patent No. 2,079,803 to Holtzclaw and Winning there is disclosed a textile oil which consists of a suitable mineral oil, preferably a white mineral oil, containing about 7% by weight of an oil soluble sulfonate and a small quantity of an ester, such as triethanolamine oleate. The patent referred to describes various compositions wherein the quantities of sulfcnates, esters, etc., may be varied somewhat and it suggests also the use of a sulfonated lard oil as a principal additive to the mineral oil. In practice, it has been found desirable to use a small quantity of water and alcohol in compositions such as described in said patent to render the triethanolamine oleate soluble in the oil. The present invention is an improvement over the invention described in said patent to Holtzclaw and Winning.
It has also been known in the prior art that certain oil soluble esters of higher polyhydric of polyhydric alcohols in rust preventing compositions. In the patent to Goodings et al., No. 2,238,882, there is disclosed a textile oil containing certain specific diesters of glycerol. The composition of the present invention is somewhat related to those of said patents but is based upon a novel combination of ingredients in controlled proportions which results in a textile oil 0 unexpected and improved properties.
It is an object of the present invention to provide an economical and efficient textile lubricant which can be easily and quite fully removed from finished goods and which combines the advantages of compositions known to the prior art and also offers advantages which have not hitherto been available. According to this invention, it is found that a particularly desirable lubricating composition may be made of mineral oil of appropriate grade, a suitable oil soluble sulfonate in proper proportions, and small controlled quantities of specific wetting or surface active agents which render the lubricants readily emulsifiable in water.
The type of emulsifying agent used according to this invention does not have the objectionable property of unduly raising the viscosity of solutions of sodium sulfonates in mineral oil. Hence, textile oils containing large amounts of sulfonates, with the corresponding improvement in securing properties, can be utilized.
In the prior art, exemplified, for instance, by the composition disclosed in the Holtzclaw and Winning Patent No. 2,079,803, difficulty has often been experienced in moving oil from the textile material after it is finished. With such compositions it has frequently been found diificult to remove more than to whereas a removal of at least to of the oil is desirable.
Textile oils prepared by dissolving large amounts (18 to 25%) of sodium sulfonate concentrate (65/35) in mineral oil can be scoured from fabric very satisfactorily. Such materials, however. do not form readily emulsifiable oils and it is necessary to add a third component to produce the required emulsibility. When this is done in accordance with the Holtzclaw and Winning patent, the viscosity of the resulting material is too high for textile processing. On the other hand, when a textile oil is prepared by dissolving 18 to 25% sodium sulionate concentrate (65/35) and made readily emulsifiable by the addition of 0.5 to 1.5% of the polyoxyethylene derivative of sorbitan mono-oleate, then its viscosity is not as high, and, furthermore, can be adjusted readily by the addition of small amounts of sorbitan mono-oleate and/or ethylene glycol monobutyl ether. It is desirable that the viscosity should be between about 100 and 300 S. S. U. at 100 F.
The following method is used in determining the quantity of oil which is removed in conven tional scouring. A 20 gram sample of cloth, previously extracted with ether to remove residual oil from previous treatments, is oiled with of its weight of oil. This oiled sample is placed in a 4-litre jar, together with one litre of scouring solution. The scouring solution consists of water containing 0.2% by weight of soap,
the usual kind being soda soaps of low titre and 0.1% of soda ash. It is maintained at a temperature of 110 F.
The jar is placed in a frame and rotated about its horizontal axis at, 50 R. P. M. for. a period of twenty minutes. After scouring, the sample is rinsed in water at about room temperature, dried, and the residual oil content determined by ether extraction. The residual oil content is expressed as the percentage of original oil applied.
EXAMPLEI A light mineral oil, for example one having a viscosity of 100 S. S. U. at 100 F. and a viscosity index of 95 attains a viscosity of 1'77 S. S. U. at 100 F. when 12% of a sodium sulfonate concentrate (65% sulfonate in mineral oil) is added. The actual sulfonate content in this case is approximately 8% by weight and the sulfonate has a molecular weight of about 460. When woolen fabrics, lubricated with 10% by weight of such an oil, are subjected to the securing test described above, 25% of the oil remains in the fabric as determined by extraction of the oil with ether. When the mahogany soap content is raised to 18% of sulfonate concentrate (i. e. about 12% sulfonate by weight) in the same mineral oil, the viscosity is increased to 205 S. S. U. at 100 F. Upon scouring in the same manner and with the same scouring liquor only 10.5% of the oil remains in the fabric. When the proportion of sodium sulfonate concentrate is increased to 24% (i. e. about 16% of actual sulfonate) the viscosity becomes 257 at 100 F. The scouring test of the high sulfonate oil is very satisfactory, only about 6.0% of residual oil being found in the finished fabric.
The above data show that textile oils prepared by dissolving sodium sulfonates in mineral oil produce very satisfactory products from the standpoint of their ability to be scoured from woolen goods. Unfortunately, such compositions do not form stable emulsions with water, and it is necessary to add an additional ingredient to impart this characteristic.
4 EXAMPIE II By the use of a combination of well-known synthetic wetting agents such as sorbitan monooleate and sorbitan mono-oleate polyoxyalkylene derivative, it has been found according to the present invention that mineral oil with 18% of sodium sulfonate concentrate (i. e. about 12% sulfonate by weight in the final product) does not have a marked increase in viscosity over the viscosity of the base mineral oil. Such a composition gives good emulsions and has excellent scouring characteristics. Best results are obtained by using small quantities of both the wetting agents referred to, although satisfactory results may be obtained by the use of only one of them. Specifically a composition was prepared by mixing together at ordinary temperatures 86.7% by weight of a mineral oil having a viscosity of S. S. U. at 100 F. and a viscosity index of 95, 12% by weight of sodium sulfonate concentrate (actually about 8% of sulfonate in the final product), 1% sorbitan monooleate polyoxyalkylene derivative, and 0.3% of sorbitan mono-oleate. This composition had a viscosity of 184 S. S. U. at 100 F., remained stable for 24 hours in a 10% emulsion and showed 23.9% residual oil after scouring with a standard scouring solution containing 0.2% of standard textile soap and 0.1% soda ash when tested in accordance with the procedure previously described.
EXAMPLE III A composition consisting of 80.5% of the same mineral oil as described above in Example II, 18.0% of sodium sulfonate concentrate as above (i. e. about 12% sodium sulfonate having average molecular weight of about 460) 1.0% of the sorbitan mono-oleate polyoxyalkylene derivative, and 0.5% of sorbitan mono-oleate. This composition has a viscosity of 202 S. S. U. at 100 F., passed the 24 hour emulsion stability test for a 10% emulsion and showed only 9.5% residual oil after scouring.
EXAMPLE IV This composition was precisely the same as that of Example 111 except that only one wetting agent was employed, that is 1.5% of sorbitan monooleate polyoxyetliylene derivative. It passed the emulsion test mentioned above satisfactorily, showed a residual content after scouring of only 9.2% of the original oil used, but its viscosity was higher, 244 S. S. U. at 100 F.
EXAMPLE v A composition was prepared containing 73.5% of the mineral oil described above, together with 25% of the sodium sulfonate concentrate, 1.0% of sorbitan mono-oleate polyoxyethylene derivative and 0.5% of sorbitan mono-oleate. It passed the emulsion test and showed a residual oil content of only 4.1% but its viscosity was 302 S. S. U. at 100 F., too high for general use.
EXANIPLEV'I In an efiort to reduce the viscosity of the composition of Example V, 1% of butyl Cellosolve (ethylene glycol monobutyl ether) was added, the mineral oil content being reduced to 72.5%. The other ingredients were the same as in Example V. This composition passed the stability test for a 10% emulsion, showed a residual oil in the fabric of only 4.8% and had a viscosity of only 219, which is satisfactory.
index in one case.
assume 5 The data given above in Examples 11 to V1 is summarized in the following table:
TABLI I Formulae and inspections of wool oils using sodium sulfonates and synthetic enmlsifier Example No II III IV V VI Formula, per cent by weight Sodium Sullonate Concentrate (65 12.0 18.0 18.0 25.0 25.0
Sorbitan mono-oleate-polyoxyethylene derivative 1.0 1.0 1 5 1.0 1.0 Sorbitan mono-oleate 0.3 0.5 0.6 0.5 Butyl Cellosolve (Ethylene glycol nonobutyl ether) 1. Mineral Oil (V./100--100 F., V.
Inspections V./100 F. (S. S. U.) 184 202 244 302 219 Emulsion test pass pass pass pass pass. Scouring Test (Per Cent Residual Oil) 23.9 9.5 9.2 4.1 4.8
1 for 24 hours.
2 Scouring liquor 0.2% soap and 0.1% soda ash.
TABLE II Securing Solution securing '5? 2; Per Cent Per Cent en Soap Soda Ash on The excellent scouring characteristics of compositions containing sodium sulfonate with synthetic emulsifiers when soda ash alone is used as the scouring agent are of particular interest. Thus, with a scouring bath containing 0.1% soda ash and no soap whatever the residual oil content was only 7.5% of the original oil used on the textile. By the use of such a composition, soap may be dispensed with as a scouring agent, which is highly desirable in the woolen trade. On the other hand, tests carried out using soap alone in the securing bath were not so satisfactory. With as much as 0.3% soap. the residual oil content was 27% and even when the soap was increased to 0.5% the residual oil was 19%.
For purposes of comparison. additional data were obtained using textile oils of the general composition described in the above-mentioned Holtzclaw and Winning patent, using various additives and using a mineral oil of lower viscosity It will be noted that only in the last two columns did the securing test show reasonably satisfactory results and in both of these cases the viscosity was extremely high, being in excess of 400 S. S. U. at 100 F. The results are shown in Table III.
Formula er cent (1 w'efiht Sodium Sulionate Concentrate (65/35). Oleic Acid Triethanolaminc Propylene Glycol.. Butyl Cellosolve (Ethylene glycol mouobutyl ether). Potassium Hydroxide. Mineral Oil, 100 S. S. U. at 100 F., 35 V. I Mineral Oil, 100 S. S. U. at 100 F.,
90 v- Hm ar:
Inspections V./ F. (S. S. U.).. Emulsion (10% for 24 hours) Securing Test, Per
Cent Residual 00..
pass
pass
pass
1 Securing bath, 0.2% soap and 0.1% soda ash.
EXAMPLE VII In order to show the usefulness of this type of textile oil for the processing of woolen goods, 9. mill test was conducted for a period of one month. Following is a description of the process:
The lubricant used had the following composition:
Per Cent Ingredient by Weig t Sodium Sulionate Concentrate (65%) 25 Sorbitan Mono-oleate 0. 5 Polyoxyethylene derivative of Sorbitan Mono-oleate 1. 5 Mineral Oil (100 S. S. U. at 100 F., 95 V. I.) 73
The wool wa's oiled with 6% by weight of the oil based on the weight of the wool in the form of a 30% aqueous emulsion. The wool was then subjected to the various processing operations. encountered in the manufacture of woolen cloth such as carding, spinning and weaving. The oil in the cloth was then removed using a scour consisting of 0.14% of soap and 0.28% soda ash.
After scouring the residual oil was 0.05% based on the dry fabric weight or 0.8% of that originally applied. After one month's service. no gumming of the steel cards was observed and. there was no apparent deterioration of the rubber and leather parts of the machines.
From the above data it will be understood that the invention contemplates the use of various quantities of sulfonates and other wetting on emulsifying agents with or without the use of a small quantity of organic solvent to reduce the over-all viscosity of the composition when such viscosity exceeds desirable limits. Thus the invention contemplates the use of a light mineral oil or mineral base oil, for example an oil of 50 to 200 S. S. U. viscosity at 100 F., preferably having a viscosity between about 75 and S. S. U. at 100 F. This oil will comprise about 70 to. 94.5% by weight of the total composition. To this is added from 5 to 20% by weight based on the total composition of a metal sulfonate, preferably an oil soluble alkali metal sulfonate. The percentage limits just referred to apply to the pure sulfonate. The sulfonate is normally added as a concentrate in mineral oil. For example 18% of a 65/35 mineral oil solution of sodium sulfonate is equivalent to 11.7% concentration of the pure sulfonate. Proportions of the concentrate added will range from about 7 to 80%. The percentage figures used in the accompanying claims refer to the pure sulionate or to a substantially pure compound, it being understood that the useful oil soluble sulionates also may be mixtures of the salts of various metals 1! desired. I
While reference has been made above to specific emulsifying agents, it will be understood that various synthetic emulsifying agents may be employed, although the fatty acid esters, and particularly the fatty acid mono-esters of polyhydric alcohols, are preferred. In particular, the fatty acid mono-ester of hexahydric alcohols are preferred, the esters of sorbitan (partially dehydrated sorbitol) being especially suitable.
It will be understood that various organic solvents may be used in proportions from about 0.1 to about 3.0%, based on the total composition, to control viscosity. The use of such solvents is advantageous when high concentrations of sulfonates are employed. In general, the invention contemplates the use of from 5 to of dry sulfonate (i. e., aside from mineral oil solvent), 0. 5 3% of synthetic emulsifying agent and 0 to 3% of the solvent. Whereas butyl Cellosolve (ethylene glycol mono-butyl ether) is specifically referred to above as the preferred solvent, other solvents may be used, the mono-alkyi ethers of ethylene glycol (known commercially as the Cellosolve compositions) being particularly preferred. The overall mineral oil content will therefore range between about 77 and 94.5% by weight.
It will be understood that various modifications may be made in the composition within the spirit of the present invention. It will also be understood that the invention contemplates improved processes for treating textile oils to secure desirable characteristics and embraces also improved techniques and processes for oiling and scouring thread, yarn, and textile materials generally.
It has been further observed that oil of the general formula of this invention is more easily removed from the fabric by the usual scouring procedure as the molecular weight 01' the sulfonates used is increased from 380 to about 480. Above 480, removal of the oil becomes more difii- 8 cult. Hence for optimum results, the sultonatee should be chosen within these limits. This re= lationship is indicated graphically in the at= tached drawing.
We claim:
1. A textile oil composition consisting essen= tially of 76 to 94.4% by weight of a mineral base oil of to 200 S. S. U. viscosity at F., 5 to 20% of sodium sulfonate having a molecular weight between 380 and 480, 0.5 to 2.5% of polyoxyalkylene derivative of sorbitan mono-oleate, and 0.1 to 1.5% of sorbitan mono-oleate.
2. A textile oil composition of low viscosity and good scouring characteristics, consisting essentially of 76 to 94.4% by weight of mineral oil oi 50 to 200 S. S. U. viscosity at 100 F., 5 to 20% of oil soluble alkali metal sulfonate having a molecular weight between 380 and 480, 0.5 to 2.5% of the polyoxyethylene derivative of sorbitan mono-oleate, and 0.1 to 1.5% of sorbitan monooleate.
3. A textile oil composition consisting essen tially of mineral oil of about 100 s. S. U. viscosity at 100 P. which contains about 6.3% by weight, based on the total composition, of sodium sulfonate having a molecular weight between 380 and 480, 1.0% of the polyoxyethylene derivative of 'sorbitan mono-oleate and 0.5% of sorbitan mono-oleate;
4. A composition according to claim 2 to which is added 0.1 to 3.0% by weight of a glycol monoether to reduce viscosity.
LORNE W. SPROULE. THOMAS W. DIXON.
REFERENCES CITED The following references are of record in the file oi! this patent:
UNITED STATES PATENTS Number Name Date 2,079,803 Holtzclaw May 11, 1937 2,436,219 MacLaurin Feb. 1'7, 1948 2,454,828 Faust Nov. 30, 1948 OTHER REFERENCES Spans and Tweens, Atlas Powder Company. Copyright 1942.

Claims (1)

1. A TEXTILE OIL COMPOSITION CONSISTING ESSENTIALLY 76 TO 94.4% BY WEIGHT OF A MINERAL BASE OIL OF 50 TO 200 S. S. U. VISCOSITY AT 100* F., 5 TO 2/% OF SODIUM SULFONATE HAVING A MOLECULAR WEIGHT BETWEEN 380 AND 480, 0.5 TO 2.5% OF POLYOXYALKYLENE DERIVATE OF SORBITAN MONO-OLEATE, AND 0.1 TO 1.5% OF SORBITAN MONO-OLEATE.
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2690426A (en) * 1950-03-07 1954-09-28 Atlas Powder Co Lubricating compositions
US2706713A (en) * 1952-06-13 1955-04-19 Exxon Research Engineering Co Textile oil
DE1021127B (en) * 1952-08-12 1957-12-19 Scottish Oils Ltd Surface-active spinning oils
US2839464A (en) * 1954-02-16 1958-06-17 Exxon Research Engineering Co Textile oil
US2850455A (en) * 1953-07-07 1958-09-02 Rhein Chemie Rheinau Gmbh Lubricating oil compositions and additives for lubricating oils
US2886532A (en) * 1954-04-15 1959-05-12 Shell Dev Hydrogen peroxide emulsions
US2911367A (en) * 1957-07-01 1959-11-03 Gulf Oil Corp Mineral lubricating oil composition
US2921027A (en) * 1957-07-26 1960-01-12 Pure Oil Co Anti-rust lubricating oil
US3125487A (en) * 1964-03-17 Bacteriostatic compositions and meth-
US3242074A (en) * 1963-03-22 1966-03-22 Eastman Kodak Co Fiber treating compositions and fibers treated therewith
US3297570A (en) * 1964-05-28 1967-01-10 Eastman Kodak Co Yarn treating compositions
US3455726A (en) * 1966-02-10 1969-07-15 Grace W R & Co Paper article coated with a slip coating of a partial ester of a fatty acid
US3458346A (en) * 1966-02-10 1969-07-29 Grace W R & Co Paper article coated with a fatty amide slip coating
US4210700A (en) * 1978-09-15 1980-07-01 Allied Chemical Corporation Production of polyester yarn
US20040007687A1 (en) * 2002-07-11 2004-01-15 Hubert Dobbelstein Formulation of a highly viscous mineral oil for the production of filters for tobacco products

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2079803A (en) * 1934-05-11 1937-05-11 Standard Oil Dev Co Soluble oil
US2436219A (en) * 1944-11-01 1948-02-17 Ind Rayon Corp Textile product and process
US2454828A (en) * 1947-07-01 1948-11-30 Sonneborn Sons Inc L Viscosity reduction of petroleum mahogany sulfonate hydrocarbon solutions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2079803A (en) * 1934-05-11 1937-05-11 Standard Oil Dev Co Soluble oil
US2436219A (en) * 1944-11-01 1948-02-17 Ind Rayon Corp Textile product and process
US2454828A (en) * 1947-07-01 1948-11-30 Sonneborn Sons Inc L Viscosity reduction of petroleum mahogany sulfonate hydrocarbon solutions

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3125487A (en) * 1964-03-17 Bacteriostatic compositions and meth-
US2690426A (en) * 1950-03-07 1954-09-28 Atlas Powder Co Lubricating compositions
US2706713A (en) * 1952-06-13 1955-04-19 Exxon Research Engineering Co Textile oil
DE1021127B (en) * 1952-08-12 1957-12-19 Scottish Oils Ltd Surface-active spinning oils
US2850455A (en) * 1953-07-07 1958-09-02 Rhein Chemie Rheinau Gmbh Lubricating oil compositions and additives for lubricating oils
US2839464A (en) * 1954-02-16 1958-06-17 Exxon Research Engineering Co Textile oil
US2886532A (en) * 1954-04-15 1959-05-12 Shell Dev Hydrogen peroxide emulsions
US2911367A (en) * 1957-07-01 1959-11-03 Gulf Oil Corp Mineral lubricating oil composition
US2921027A (en) * 1957-07-26 1960-01-12 Pure Oil Co Anti-rust lubricating oil
US3242074A (en) * 1963-03-22 1966-03-22 Eastman Kodak Co Fiber treating compositions and fibers treated therewith
US3297570A (en) * 1964-05-28 1967-01-10 Eastman Kodak Co Yarn treating compositions
US3455726A (en) * 1966-02-10 1969-07-15 Grace W R & Co Paper article coated with a slip coating of a partial ester of a fatty acid
US3458346A (en) * 1966-02-10 1969-07-29 Grace W R & Co Paper article coated with a fatty amide slip coating
US4210700A (en) * 1978-09-15 1980-07-01 Allied Chemical Corporation Production of polyester yarn
US20040007687A1 (en) * 2002-07-11 2004-01-15 Hubert Dobbelstein Formulation of a highly viscous mineral oil for the production of filters for tobacco products
US7153447B2 (en) * 2002-07-11 2006-12-26 Emini Shefqet Formulation of a highly viscous mineral oil for the production of filters for tobacco products

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