US3122502A - Stabilized germicidal textile softeners - Google Patents

Stabilized germicidal textile softeners Download PDF

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US3122502A
US3122502A US61405A US6140560A US3122502A US 3122502 A US3122502 A US 3122502A US 61405 A US61405 A US 61405A US 6140560 A US6140560 A US 6140560A US 3122502 A US3122502 A US 3122502A
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Milton M Waldman
Brow Paul L Du
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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
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • 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
    • D06M16/00Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic

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  • This invention relates to liquid laundry preparations and particularly it relates to highly stable aqueous combinations of cationic fabric softeners and germicides, and to processes for preparing them.
  • additives may be advantageously incorporated into textiles during laundering.
  • Such additives include fabric brighteners, bluing dyes, optical brighteners, reWet agents and germicides.
  • These additives may be incorporated by a padding process or by substantive laundering.
  • the additive is commonly dispersed or dissolved in a liquid medium at a suitable concentration based on the volume of the liquid, the fabric contacted with the liquid, and the liquid medium removed from the fabric by evaporation.
  • Additives that do not display substantivity must ordinarily be incorporated into the fabric by padding which is usually costly and troublesome.
  • it is often difficult to obtain uniform distribution of materials applied by padding due to the fact that they are not attracted to the fabrics but are merely deposited upon the cloth during removal of the liquid medium.
  • the substantive additive which has an afiinity for the fibers of the fabric, is usually dispersed or dissolved in rinse or wash water at a suitable concentration based on the amount of fabric and irrespective of the water volume. Effective concentrations of the additive become bonded to the fabric even though the substantive additive is present in the water at relatively low concentrations.
  • Cationic fabric softeners are commonly dispersed in rinse water during laundering. Clothing rinsed in a fabric softener is faster drying, shows reduced wrinkling, is desirably flulr'ed or softened, and has improved antistatic properties. Cationic softeners, however, are only minimally effective as germicidal agents. Sanitizing treatment of clothing and textile is of recognized importance. Infections, such as those of Staphylococcus origin causing vexatious problems on institutions and hospitals, may be alleviated by use of proper germicidal laundering practices. 111 homes as well as institutions and hospitals, clothing, diapers and bed linens may be advantageously sanitized by treatment with gerrnicides.
  • Certain relatively water insoluble compounds such as organomercurial compounds have been found quite suitable as germicidal sanitizing agents in laundering, despite their toxicity at high concentrations. Textiles containing such germicidal salts effectively inhibit growth of pathogenic organisms.
  • liquid preparations of laundering additives are most convenient, rather dilute. products generally being supplied for home'use and more concentrated products supplied for commercial use. Ease of measuring and ready water miscibility are advantages inherent to liquid preparations. Fluidity of such products is an important quality feature, although such fluidity normally renders the preparations less stable. Such instability presents serious manufacturing problems in that separation of substituents during distribution and use cannot be tolerated from either the esthetic or safety viewpoint. Settling of the heavy, insoluble organomercurial germicidal compounds may lead to the incorporation of excessive levels of germicide in clothing. Excessive quantities of the germicides in fabrics which are in intimate contact with body surfaces may cause severe toxic manifestations. Therefore, it is highly desirable to have available stable fiuid preparations of germicidal liquid softeners in which settling-out of toxic substituents is minimized and held within acceptable limits.
  • organomercurial gerrnicides being only minimally substantive to textiles are difiicult to uniformly distribute onto fabrics, thus making it ordinarily necessary to incorporate them by means of a padding process.
  • organomercurial'germicides dispersed in a fluid cationic textile softener preparation maybe uniformly afiixed to clothing in effective concentrations from a relatively dilute dispersion of the germicidal material.
  • Cationic softeners are substantive toward fabric fibers and when combined with organomercurial compounds are attracted and bonded to the fibers in conjunction with the mercurial compounds, in effect rendering the germicides in the combination highly substantive toward fabrics being treated.
  • the preparations may be rendered stable during storage and use, thus obviating separation difliculties and the danger of germicidal settling.
  • a fluid colloidal preparation comprising at least one cationic fabric softener which is preferentially absorbed by'cloth, at least one'organomercurial germicide, and a minor portion of thin boiling cornstarch which is present at concentrations not appreciably affecting fluidity of the combination but at concentrationseffective to cause the germicide to remain evenly dispersed throughout the colloid.
  • the cationic softener exerts a potentiating effect upon the germicidal activity of the organomercurial compound as well as aiding in more uniform absorption of germicide onto fabrics.
  • a cationic fabric softener is dispersed or dissolved in water or other suitable liquid.
  • the cationic compounds which function as suitable textile softeners are quaternary ammonium compounds containing at least twdalkyl chains having about 16 to about 22 carbon atoms irreach chain, and which may contain ethylene oxide. Examples of such compounds include distearylrnethyltriethoxyethanolam- .monium methyl sulfate, dimethyldih'ydrogenatedtallowquaternaryammonium chloride, stearyldialkanolalkylbenzylammonium chloride, and quate'rnize d' imidazoline compounds.
  • Examples of commerciallyavailablesofteners are those sold under the following trademarks: Arquad U 2HT, Softener 2-132, Aliquat 226, Adogen 442, Marcoquat-75 and Oversoft D.
  • Arquad U 2HT Arquad U 2HT
  • Softener 2-132 Aliquat 226, Adogen 442, Marcoquat-75
  • Oversoft D We prefer to use dialkyldimethylammonium chloride and optimally use the dimethyldistearyl quaternary ammonium chloride sold under the trademark Arquad 2HT.
  • Concentration of softener should optimally be suflicient to give a final concentration of about 0.05 to 0.3% softener based on weight of fabric to be treated.
  • a water dispersible preparation containing from about 2% to 50% or 2 to 50 parts of active softener by weight is adequate for all types of usage. For individual use concentrations from about 2% to 8% active softener are preferred, while commercial laundries often prefer more concentrated products which are diluted before use. We prefer to have about 4% active softener in the final fluid preparation.
  • An organomercurial germicide is combined with a liquid preparation of softener.
  • any organomercurial germicide may be used in our invention, we find that best results are obtained with phenylmercuric salts such as the acetate, butyrate, bromide, chloride, iodide, propionate, and the like.
  • a concentration of 0.02 to 5 parts by weight is operable.
  • phenylmercuric propionate in a dimethyldistearyl quaternary ammonium softener.
  • concentration of germicide to softener may be optimally adjusted dependent on the molecular weight of the salt compared to the percentage of mercury in the salt.
  • the softener-germicide combination is incorporated into a colloid formed by modified starch which prevents separation of the combined substituents.
  • modified starch which prevents separation of the combined substituents.
  • thin boiling cornstarch which has been treated to reduce its fluidity, for example by acid modification or chlorination, will satisfactorily stabilize the compositions of this invention.
  • acid modified cornstarch having a fluidity number of from about 5 to about 40.
  • the grade, type and amount of cornstarch optimally suited to a specific combination varies to some degree.
  • Sufiicient cornstarch must be incorporated into the germicide-softener combination to adequately stabilize it for suitable periods of time while maintaining product fluidity in the range of about less than 500 centipoises.
  • the colloidal concentration required is dependent to a substantial degree on the concentration of the softener.
  • the concentration becomes critical when very dilute softener dispersions are prepared because of their tendency to be quite unstable.
  • Use of a concentration of about 0.5 to 1.5% or 0.5 to 1.5 parts of starch by weight of the total formula tion satisfactorily prevents precipitation of the organomercurial compound or salting out of the softener.
  • We find that especially good results are obtained by using 0.5 to 1.5% or 0.5 to 1.5 parts of acid modified starch in combinations containing about 4% active cationic surface active compounds.
  • the balance of the softener composition is water. About 43.5 to about 97.4 parts of water are required.
  • the starch In preparing the compositions of this invention the starch should be added to water and boiled for several minutes to insure complete gelatinization.
  • the melted cationic softener preferably with the germicide dispersed therein, may then be added to the colloidal starch preparation.
  • the germicide may be easily dispersed in the softener by mixing a slurry of the two ingredients with hexylene glycol. Additional ingredients such as rewet agents, dyes, perfumes and other optional additives may be added before or after the addition of the softener compound.
  • Water soluble ingredients such as bluing dyes and brighteners should ordinarily be added before the softener.
  • Alcohol soluble brighteners and like additives should ordinarily be added at the end of the dispersing operation.
  • Example I A typical home laundry preparation having the following formula by weight was prepared:
  • Example 11 Using the procedure of Example I a softener-germicidal combination having the following formula was prepared:
  • the viscosity of this preparation after thorough mixing was determined to be 40 centipoises when measured by means of a Brookfield viscosimeter. Within 24 hours after mixing, essentially all of the mercurial salt had been precipitated from the mixture.
  • a second preparation was prepared using the above.
  • Example III There may be employed in the compositions of this invention formulations similar to that of Example II except that phenylmercuric acetate is used instead of phenylmercuric propionate.
  • Example IV There may be used in the compositions of this invention formulations similar to that of Example II except that phenylmercuric butyrate is used instead of phenylmercuric propionate.
  • Example V There may be employed in the compositions of this invention formulations similar to that of Example II except that phenylmercuric chloride is substituted for.
  • Example VI There may be employed in the compositions of this invention formulations similar to that of Example II except that stearyldialkanolalkylbenzyl ammonium chloride may be used as the softener instead of dimethyldistearyl quaternary ammonium chloride.
  • Example VII There may be employed in the compositions of this invention formulations similar to that of Example II except that distearylmethyltriethoxyethanol ammonium methosulfate may be used instead of dimethyldistearyl quaternary ammonium compound.
  • Example VIII There may be employed in the compositions of this invention a formulation similar to that of Example II except that a quaternized imidazoline compound may be used in place of the dimethyldistearyl quaternary compound.
  • a germicidal liquid fabric softener composition which is stable and substantive to fabric when dissolved in the wash waters of the fabric during laundering, said softener composition consisting essentially of about 2 to 50 parts by weight of a cationic fabric softener consisting of a quaternary ammonium compound having two alkyl chains of about 16 to 22 carbon atoms in each chain, one part by weight of a substantially water insoluble phenylmercuric salt per 10 to 100 parts of said 6 fabric softener and 0.5 to 1.5 parts by Weight of acid modified starch, the balance of said composition being water.
  • a germicidal fabric softener composition which is stable and substantive to fabric when dissolved in the wash waters of the fabric during laundering, said softener composition consisting essentially of about 2 to 50 parts by weight of a cationic fabric softener consisting of a quaternary ammonium compound having two alkyl chains of about 16 to about 22 carbon atoms in each chain, about 0.02 to 5 parts by weight of a substantially water insoluble phenylmercuric salt, about 0.5 to about 1.5 parts gelatinized acid modified cornstarch and about 43.5 to about 97.4 parts water.

Description

United States Patent 3,122,502 STABHJEZED GERWHCEDAL TEXTILE SQFTENERS Milton M. Waldman, 229 Southgate Drive, Northbroolr, ILL, and Paul L. Du Brow, 3114 S. Merrill, Chicago, Ill. No Drawing. Filed Oct. 10, 196i), Ser. No. 61,405 5 Claims. (Cl. 252--3.8)
This invention relates to liquid laundry preparations and particularly it relates to highly stable aqueous combinations of cationic fabric softeners and germicides, and to processes for preparing them.
Numerous additives may be advantageously incorporated into textiles during laundering. Such additives include fabric brighteners, bluing dyes, optical brighteners, reWet agents and germicides. These additives may be incorporated by a padding process or by substantive laundering. In a padding process the additive is commonly dispersed or dissolved in a liquid medium at a suitable concentration based on the volume of the liquid, the fabric contacted with the liquid, and the liquid medium removed from the fabric by evaporation. Additives that do not display substantivity must ordinarily be incorporated into the fabric by padding which is usually costly and troublesome. Also, it is often difficult to obtain uniform distribution of materials applied by padding due to the fact that they are not attracted to the fabrics but are merely deposited upon the cloth during removal of the liquid medium.
Home and commercial laundering is generally performed on a substantive basis. The substantive additive, which has an afiinity for the fibers of the fabric, is usually dispersed or dissolved in rinse or wash water at a suitable concentration based on the amount of fabric and irrespective of the water volume. Effective concentrations of the additive become bonded to the fabric even though the substantive additive is present in the water at relatively low concentrations.
Cationic fabric softeners are commonly dispersed in rinse water during laundering. Clothing rinsed in a fabric softener is faster drying, shows reduced wrinkling, is desirably flulr'ed or softened, and has improved antistatic properties. Cationic softeners, however, are only minimally effective as germicidal agents. Sanitizing treatment of clothing and textile is of recognized importance. Infections, such as those of Staphylococcus origin causing vexatious problems on institutions and hospitals, may be alleviated by use of proper germicidal laundering practices. 111 homes as well as institutions and hospitals, clothing, diapers and bed linens may be advantageously sanitized by treatment with gerrnicides. Certain relatively water insoluble compounds such as organomercurial compounds have been found quite suitable as germicidal sanitizing agents in laundering, despite their toxicity at high concentrations. Textiles containing such germicidal salts effectively inhibit growth of pathogenic organisms.
For general use, liquid preparations of laundering additives are most convenient, rather dilute. products generally being supplied for home'use and more concentrated products supplied for commercial use. Ease of measuring and ready water miscibility are advantages inherent to liquid preparations. Fluidity of such products is an important quality feature, although such fluidity normally renders the preparations less stable. Such instability presents serious manufacturing problems in that separation of substituents during distribution and use cannot be tolerated from either the esthetic or safety viewpoint. Settling of the heavy, insoluble organomercurial germicidal compounds may lead to the incorporation of excessive levels of germicide in clothing. Excessive quantities of the germicides in fabrics which are in intimate contact with body surfaces may cause severe toxic manifestations. Therefore, it is highly desirable to have available stable fiuid preparations of germicidal liquid softeners in which settling-out of toxic substituents is minimized and held within acceptable limits.
The organomercurial gerrnicides being only minimally substantive to textiles are difiicult to uniformly distribute onto fabrics, thus making it ordinarily necessary to incorporate them by means of a padding process. We have found that organomercurial'germicides dispersed in a fluid cationic textile softener preparation maybe uniformly afiixed to clothing in effective concentrations from a relatively dilute dispersion of the germicidal material. Cationic softeners are substantive toward fabric fibers and when combined with organomercurial compounds are attracted and bonded to the fibers in conjunction with the mercurial compounds, in effect rendering the germicides in the combination highly substantive toward fabrics being treated.
We have further discovered that by stabilizing the softener-germicide liquid preparations with minor portions of thin boiling cornstarch, which has no appreciably detrimental effect on the fluidity of the final preparation, the preparations may be rendered stable during storage and use, thus obviating separation difliculties and the danger of germicidal settling.
Consequently, it is an important object of this invention to provide highly stable liquid preparations for simultaneously and substantively sanitizing and softening fabrics. Other objects and advantages Will appear as this specification proceeds.
To this end, and in accordance with our invention, there is provided a fluid colloidal preparation comprising at least one cationic fabric softener which is preferentially absorbed by'cloth, at least one'organomercurial germicide, and a minor portion of thin boiling cornstarch which is present at concentrations not appreciably affecting fluidity of the combination but at concentrationseffective to cause the germicide to remain evenly dispersed throughout the colloid. The cationic softener exerts a potentiating effect upon the germicidal activity of the organomercurial compound as well as aiding in more uniform absorption of germicide onto fabrics.
Accordingly, in the practice of our invention a cationic fabric softener is dispersed or dissolved in water or other suitable liquid. Generally the cationic compounds which function as suitable textile softeners are quaternary ammonium compounds containing at least twdalkyl chains having about 16 to about 22 carbon atoms irreach chain, and which may contain ethylene oxide. Examples of such compounds include distearylrnethyltriethoxyethanolam- .monium methyl sulfate, dimethyldih'ydrogenatedtallowquaternaryammonium chloride, stearyldialkanolalkylbenzylammonium chloride, and quate'rnize d' imidazoline compounds. Examples of commerciallyavailablesofteners are those sold under the following trademarks: Arquad U 2HT, Softener 2-132, Aliquat 226, Adogen 442, Marcoquat-75 and Oversoft D. We prefer to use dialkyldimethylammonium chloride and optimally use the dimethyldistearyl quaternary ammonium chloride sold under the trademark Arquad 2HT.
Concentration of softener should optimally be suflicient to give a final concentration of about 0.05 to 0.3% softener based on weight of fabric to be treated. A water dispersible preparation containing from about 2% to 50% or 2 to 50 parts of active softener by weight is adequate for all types of usage. For individual use concentrations from about 2% to 8% active softener are preferred, while commercial laundries often prefer more concentrated products which are diluted before use. We prefer to have about 4% active softener in the final fluid preparation.
An organomercurial germicide is combined with a liquid preparation of softener. Although any organomercurial germicide may be used in our invention, we find that best results are obtained with phenylmercuric salts such as the acetate, butyrate, bromide, chloride, iodide, propionate, and the like. A concentration of 0.02 to 5 parts by weight is operable. We prefer to use a phenylmercuric salt in a ratio of about 1 part of salt to about 13 to 20 parts of cationic softener, although one part of salt per to 100 parts of softener or 0.002 to 5 parts of the total composition may be used. Optimally, we prefer to use this ratio of phenylmercuric propionate in a dimethyldistearyl quaternary ammonium softener. Variations in concentration of germicide to softener may be optimally adjusted dependent on the molecular weight of the salt compared to the percentage of mercury in the salt.
The softener-germicide combination is incorporated into a colloid formed by modified starch which prevents separation of the combined substituents. We have found that thin boiling cornstarch which has been treated to reduce its fluidity, for example by acid modification or chlorination, will satisfactorily stabilize the compositions of this invention. We prefer to use acid modified cornstarch having a fluidity number of from about 5 to about 40. The grade, type and amount of cornstarch optimally suited to a specific combination varies to some degree. Sufiicient cornstarch must be incorporated into the germicide-softener combination to adequately stabilize it for suitable periods of time while maintaining product fluidity in the range of about less than 500 centipoises. The colloidal concentration required is dependent to a substantial degree on the concentration of the softener. The concentration becomes critical when very dilute softener dispersions are prepared because of their tendency to be quite unstable. Use of a concentration of about 0.5 to 1.5% or 0.5 to 1.5 parts of starch by weight of the total formula tion satisfactorily prevents precipitation of the organomercurial compound or salting out of the softener. We find that especially good results are obtained by using 0.5 to 1.5% or 0.5 to 1.5 parts of acid modified starch in combinations containing about 4% active cationic surface active compounds.
The balance of the softener composition is water. About 43.5 to about 97.4 parts of water are required.
In preparing the compositions of this invention the starch should be added to water and boiled for several minutes to insure complete gelatinization. The melted cationic softener, preferably with the germicide dispersed therein, may then be added to the colloidal starch preparation. The germicide may be easily dispersed in the softener by mixing a slurry of the two ingredients with hexylene glycol. Additional ingredients such as rewet agents, dyes, perfumes and other optional additives may be added before or after the addition of the softener compound. Water soluble ingredients such as bluing dyes and brighteners should ordinarily be added before the softener. Alcohol soluble brighteners and like additives should ordinarily be added at the end of the dispersing operation.
The following specific examples will serve to further illustrate our invention:
Example I A typical home laundry preparation having the following formula by weight was prepared:
Percent Arquad 2 HT- 5.34 Calcofluour White M2R New (brightener dye) 0.05 Hidacid Azure Blue 20-2204 (bluing dye) 0.0025 Phenylmercuric propionate 0.2 Acetic acid 0.1
No. 20 acid modified thin boiled starch-Amaizo TB-20 Hexylene glycol 0.5 Water Q.S.
Total llrademark for dimethyldistearyl quaternary ammonium chloride manufactured by Armour and Company, 7 5% active Example 11 Using the procedure of Example I a softener-germicidal combination having the following formula was prepared:
Percent Dimethyldistearyl quaternary ammonium chloride 4 Hexylene glycol 0.5 Phenylmercuric propionate 0.2
Water 95.3
The viscosity of this preparation after thorough mixing was determined to be 40 centipoises when measured by means of a Brookfield viscosimeter. Within 24 hours after mixing, essentially all of the mercurial salt had been precipitated from the mixture.
A second preparation was prepared using the above.
formula, but having in addition 1% #20 acid modified cornstarch. Fluidity of the stabilized preparation measured 40 centipoises on a Brookfield viscosimeter. After, 6 months storage no sediment was visible in the prepara tion; essentially all of the mercurial salt remained in suspension.
Example III There may be employed in the compositions of this invention formulations similar to that of Example II except that phenylmercuric acetate is used instead of phenylmercuric propionate.
Example IV There may be used in the compositions of this invention formulations similar to that of Example II except that phenylmercuric butyrate is used instead of phenylmercuric propionate.
Example V There may be employed in the compositions of this invention formulations similar to that of Example II except that phenylmercuric chloride is substituted for.
phenylmercuric propionate.
Example VI There may be employed in the compositions of this invention formulations similar to that of Example II except that stearyldialkanolalkylbenzyl ammonium chloride may be used as the softener instead of dimethyldistearyl quaternary ammonium chloride.
Example VII There may be employed in the compositions of this invention formulations similar to that of Example II except that distearylmethyltriethoxyethanol ammonium methosulfate may be used instead of dimethyldistearyl quaternary ammonium compound.
Example VIII There may be employed in the compositions of this invention a formulation similar to that of Example II except that a quaternized imidazoline compound may be used in place of the dimethyldistearyl quaternary compound.
While in the foregoing specification various embodiments of this invention have been described in consider: able detail for the purpose of illustration, it will be apparent to those skilled in the art that this invention is susceptible to other embodiments and that many of these details can be widely varied without departing from the basic concept and spirit of the invention.
We claim:
1. A germicidal liquid fabric softener composition which is stable and substantive to fabric when dissolved in the wash waters of the fabric during laundering, said softener composition consisting essentially of about 2 to 50 parts by weight of a cationic fabric softener consisting of a quaternary ammonium compound having two alkyl chains of about 16 to 22 carbon atoms in each chain, one part by weight of a substantially water insoluble phenylmercuric salt per 10 to 100 parts of said 6 fabric softener and 0.5 to 1.5 parts by Weight of acid modified starch, the balance of said composition being water.
2. A germicidal fabric softener composition which is stable and substantive to fabric when dissolved in the wash waters of the fabric during laundering, said softener composition consisting essentially of about 2 to 50 parts by weight of a cationic fabric softener consisting of a quaternary ammonium compound having two alkyl chains of about 16 to about 22 carbon atoms in each chain, about 0.02 to 5 parts by weight of a substantially water insoluble phenylmercuric salt, about 0.5 to about 1.5 parts gelatinized acid modified cornstarch and about 43.5 to about 97.4 parts water.
3. The softener composition of claim 2 wherein said salt is phenylmercuric propionate.
4. The softener composition of claim 2 wherein said cationic softener is dimethyldistearyl quaternary ammonium chlon'de.
, 5. The softener composition of claim 2 wherein said cornstarch has a fluidity number of between 5 and 40.
References Cited in the file of this patent UNITED STATES PATENTS 2,480,084 Meyer Aug. 23, 1949 2,826,506 Trusler Mar. 11, 1958 2,830,011 Parker Apr. 8, 1958 2,831,853 Satterly Apr. 22, 1958 2,876,140 Sheehan Mar. 3, 1959 2,880,129 Billings Mar. 31, 1959 OTHER REFERENCES Arquads, published by Armour and Co., 3 pages, received February 1950.

Claims (1)

1. A GERMICIDAL LIQUID FABRIC SOFTENER COMPOSITION WHICH IS STABLE AND SUBSTANTIVE TO FABRIC WHEN DISSOLVED IN THE WASH WATERS OF THE FABRIC DURING LAUNDERING, SAID SOFTENER COMPOSITION CONSISTING ESSENTIALLY OF ABOUT 2 TO 50 PARTS BY WEIGHT OF A CATIONIC FABRIC SOFTENER CONSISTING OF A QUATERNARY AMMONIUM COMPOUND HAVING TWO ALKYL CHAINS OF ABOUT 16 TO 22 CARBON ATOMS IN EACH CHAIN, ONE PART BY WEIGHT OF A SUBSTANTIALLY WATER INSOLUBLE PHENYLMERCURIC SALT PER 10 TO 100 PARTS OF SAID FABRIC SOFTENER AND 0.5 TO 1.5 PARTS BY WEIGHT OF ACID MODIFIED STARCH, THE BALANCE OF SAID COMPOSITION BEING WATER.
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Cited By (11)

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US3279980A (en) * 1964-02-28 1966-10-18 Great Lakes Biochemical Co Inc Composition for and method of treating water
US3325404A (en) * 1963-09-19 1967-06-13 Millmaster Onyx Corp Composition for simultaneously laundering and softening fabrics
US3360470A (en) * 1963-05-28 1967-12-26 Colgate Palmolive Co Laundering compositions
US3364142A (en) * 1965-12-06 1968-01-16 Northern Petro Chem Co Composition for reconstituting frozen aqueous systems and method for making
US3395100A (en) * 1964-12-11 1968-07-30 Foremost Mckesson Fabric softener and method of using
US3442695A (en) * 1964-07-16 1969-05-06 Gen Mills Inc Compounds as textile softeners
US3509049A (en) * 1965-11-01 1970-04-28 Geigy Chem Corp Fabric softening and brightening compositions
US3637495A (en) * 1966-08-01 1972-01-25 Henkel & Cie Gmbh Agent for the posttreatment of laundry
US3644204A (en) * 1967-08-14 1972-02-22 Henkel & Cie Gmbh Agent for the post-treatment of washed laundry
US3904533A (en) * 1963-07-16 1975-09-09 Lever Brothers Ltd Fabric conditioners
US3997453A (en) * 1974-02-11 1976-12-14 Colgate-Palmolive Company Softener dispersion

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US2480084A (en) * 1948-03-20 1949-08-23 Dow Chemical Co Protection of cellulosic textile materials
US2826506A (en) * 1952-12-05 1958-03-11 Davies Young Soap Company Composition for treating fibrous materials
US2830011A (en) * 1957-02-07 1958-04-08 American Cyanamid Co Textile fabrics containing neomycin
US2831853A (en) * 1953-10-07 1958-04-22 Standard Brands Inc Manufacture of sizing
US2876140A (en) * 1955-06-30 1959-03-03 Bibb Mfg Company Soil resistant textile material and method of making the same
US2880129A (en) * 1956-01-19 1959-03-31 Johnson & Johnson Imparting anti-microbial properties to formed articles

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2480084A (en) * 1948-03-20 1949-08-23 Dow Chemical Co Protection of cellulosic textile materials
US2826506A (en) * 1952-12-05 1958-03-11 Davies Young Soap Company Composition for treating fibrous materials
US2831853A (en) * 1953-10-07 1958-04-22 Standard Brands Inc Manufacture of sizing
US2876140A (en) * 1955-06-30 1959-03-03 Bibb Mfg Company Soil resistant textile material and method of making the same
US2880129A (en) * 1956-01-19 1959-03-31 Johnson & Johnson Imparting anti-microbial properties to formed articles
US2830011A (en) * 1957-02-07 1958-04-08 American Cyanamid Co Textile fabrics containing neomycin

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3360470A (en) * 1963-05-28 1967-12-26 Colgate Palmolive Co Laundering compositions
US3904533A (en) * 1963-07-16 1975-09-09 Lever Brothers Ltd Fabric conditioners
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