US3464847A - Treatment of fabrics with anthranilic acid and silver nitrate solutions - Google Patents

Treatment of fabrics with anthranilic acid and silver nitrate solutions Download PDF

Info

Publication number
US3464847A
US3464847A US3464847DA US3464847A US 3464847 A US3464847 A US 3464847A US 3464847D A US3464847D A US 3464847DA US 3464847 A US3464847 A US 3464847A
Authority
US
United States
Prior art keywords
anthranilic acid
fabric
silver nitrate
fabrics
silver
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
Inventor
Frederic H Megson
Michael T Beachem
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
US Department of Army
Original Assignee
US Department of Army
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by US Department of Army filed Critical US Department of Army
Application granted granted Critical
Publication of US3464847A publication Critical patent/US3464847A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • D06M13/325Amines
    • D06M13/342Amino-carboxylic acids; Betaines; Aminosulfonic acids; Sulfo-betaines
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2508Coating or impregnation absorbs chemical material other than water
    • Y10T442/2516Chemical material is one used in biological or chemical warfare

Definitions

  • the present invention relates to an improved method for imparting antivesicant properties to cellulosic fabrics and more particularly to imparting antivesicant properties to cellulosic fabrics by impregnating or modifying them with chelates derived from anthranilic acid and silver nitrate.
  • Vesicant agents such as mustard gas, attack the skin as well as the respiratory system of exposed personnel. Therefore, a body shield, in addition to a protective mask, is essential to prevent casualties.
  • a fabric impermeable to all fluids would afford complete protection, but would be impractical, especially in warm climates, for extended periods of wear. More preferable is protection built into occupational clothing; thereby permitting air circulation and preventing moisture accumulation.
  • Mustard gas is the term applied to the well-known vesicant, bis(2-chloroethyl) sulfide.
  • Standard mustard gas exists as a vapor or as airborne droplets.
  • Various processes and compounds have been suggested and employed to impart finishes to the fabric used for military uniforms which would deactivate mustard gas and would prevent its passage through the cloth. But the efficiency of prior methods leaves much to be desired.
  • the N-chloroamides are the N-chloroamides. Once on the fabric, these compounds lose activation by hydrolysis, atmospheric moisturization, perspiration, thermal decomposition, and the like.
  • the present invention is premised on the discovery that certain silver chelates or complexes, particularly those of anthranilic acid, are effective agents for applying to fabrics and for imparting superior antivesicant properties thereto. Accordingly, it is among the objects of the present invention to provide a treatment for air-permeable cellulosic fabric materials that will prevent passage of vesicant agent vapors through the garment. It is another object to provide a noninjurious finish for such fabric materials which requires no further treatment by the wearer for antivesicant protection. It is a final object to provide a vesicant-resistant treatment for textile fabrics that is relatively stable and that does not adversely afiect the tensile strength of the fabric.
  • the silver compounds employed in the method of the instant invention provide surprisingly effective results. Their use produces effective fabric barriers to mustard gas which are stable to moisture and to temperature up to about 150 C. The mustard gas is inactivated and its passage prevented through the cellulosic cloth.
  • the high effectiveness of the silver chelates or complexes of anthranilic acid is unexpected in view of the slight effectiveness of anthranilic acid itself and of other metal chelates of anthranilic acid such as copper and iron.
  • the invention is practiced by padding a solution of anthranilic acid onto the fabric, air drying, treating the fabric with silver nitrate solution, and drying once more.
  • the padding process involves submerging the fabric in the solution, permitting it to soak for a few minutes, and gently squeezing it between rollers.
  • the degree of antivesicant effect is adjusted by the amount of silver anthranilic complex applied.
  • a possible alternative to the method set forth above is to first form the complex by reaction of anthranilic acid with silver nitrate and then apply the reaction product by padding a solution or dispersion thereof on the fabric.
  • the efficiency of the mustard gas barrier is determined by the Dawson Testa measurement of the percent of mustard gas, initially present in an air stream, retained on a fabric after air passage through the fabric.
  • Table I following Example I depicts the relative elfectiveness of the silver derivative of anthranilic acid as compared with anthranilic acid itself and with the copper and iron derivatives; all applied as prescribed in Example I.
  • This crude product consists of 11.2 parts of sparkling light brown crystals which decompose sharply at 160 C. with the immediate formation of a silver mirror.
  • the crude is extracted with 100 parts by volume of boiling anhydrous- 2B alcohol and dried at 5055 C.; 10.6 parts of sparkling gray violet crystals result. These crystals also decompose sharply at C. with the concomitant formation of a silver mirror.
  • Analysis disclosed a product having an empirical formula C H N O Ag The product so formed is applied by padding 9. disper sion of it on the fabric. In a standard test procedure, 60 micrograms of mustard gas treated with 4000 micrograms of the product was completely inactivated.
  • EXAMPLE III The alcohol filtrate from Example II, when permitted to stand overnight at room temperature deposits 27.8 parts of large light violet crystals. These are purified by dissolving in 250 parts by volume of boiling anhydrous 2B alcohol clarifying with adsorbent charcoal, concentrating the filtrate to a small volume, filtering at room temperature, washing the crystals with alcohol, and drying overnight at 50-55 C.
  • the recrystallized product consists of 14.0 parts of light violet crystals which melt at 155158 C., evolve gas, but dont form a silver mirror. Analysis shows the empirical formula to be CqHqN2O5Ag.
  • the product is applied to the cloth as a dispersion by padding as in Example II. It gives standard test results identical with the product of Example II total inactivation of mustard gas.
  • An air permeable fabric vested with antivesicant properties comprising a fabric treated with the reaction products of silver nitrate and anthranilic acid.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

United States Patent 3,464,847 TREATMENT OF FABRICS WITH ANTHRANILIC ACID AND SILVER NlTRATE SOLUTIONS Frederic H. Megson, Martinsville, and Michael T.
Beachem, Somerset, N.J., assignors, by mesne assignments, to the United States of America as represented by the Secretary of the Army No Drawing. Filed Oct. 25, 1966, Ser. No. 589,473 Int. Cl. C08j N38 US. Cl. 117-121 7 Claims ABSTRACT OF THE DISCLOSURE A method for imparting antivesicant properties to air permeable fabrics, comprising treating the fabrics with a solution of anthranilic acid and silver nitrate.
The present invention relates to an improved method for imparting antivesicant properties to cellulosic fabrics and more particularly to imparting antivesicant properties to cellulosic fabrics by impregnating or modifying them with chelates derived from anthranilic acid and silver nitrate.
Vesicant agents, such as mustard gas, attack the skin as well as the respiratory system of exposed personnel. Therefore, a body shield, in addition to a protective mask, is essential to prevent casualties. A fabric impermeable to all fluids would afford complete protection, but would be impractical, especially in warm climates, for extended periods of wear. More preferable is protection built into occupational clothing; thereby permitting air circulation and preventing moisture accumulation.
Mustard gas is the term applied to the well-known vesicant, bis(2-chloroethyl) sulfide. Standard mustard gas exists as a vapor or as airborne droplets. Various processes and compounds have been suggested and employed to impart finishes to the fabric used for military uniforms which would deactivate mustard gas and would prevent its passage through the cloth. But the efficiency of prior methods leaves much to be desired. For example, among the most commonly used are the N-chloroamides. Once on the fabric, these compounds lose activation by hydrolysis, atmospheric moisturization, perspiration, thermal decomposition, and the like.
The present invention is premised on the discovery that certain silver chelates or complexes, particularly those of anthranilic acid, are effective agents for applying to fabrics and for imparting superior antivesicant properties thereto. Accordingly, it is among the objects of the present invention to provide a treatment for air-permeable cellulosic fabric materials that will prevent passage of vesicant agent vapors through the garment. It is another object to provide a noninjurious finish for such fabric materials which requires no further treatment by the wearer for antivesicant protection. It is a final object to provide a vesicant-resistant treatment for textile fabrics that is relatively stable and that does not adversely afiect the tensile strength of the fabric. These and other objects and advantages of the, instant invention will be fully apparent from the following description and examples.
The silver compounds employed in the method of the instant invention provide surprisingly effective results. Their use produces effective fabric barriers to mustard gas which are stable to moisture and to temperature up to about 150 C. The mustard gas is inactivated and its passage prevented through the cellulosic cloth. The high effectiveness of the silver chelates or complexes of anthranilic acid is unexpected in view of the slight effectiveness of anthranilic acid itself and of other metal chelates of anthranilic acid such as copper and iron.
Patented Sept. 2, 1969 "ice In its simplest form, the invention is practiced by padding a solution of anthranilic acid onto the fabric, air drying, treating the fabric with silver nitrate solution, and drying once more. The padding process involves submerging the fabric in the solution, permitting it to soak for a few minutes, and gently squeezing it between rollers. The degree of antivesicant effect is adjusted by the amount of silver anthranilic complex applied. Although the exact nature of the silver complex which affords the vesicant protection has not been completely identified, it is probably at least one of the following: the silver nitrate complex of the silver salt, the silver salt of anthranilic acid, and the nitric acid salt of the silver complex. Each of these are formularized below:
A possible alternative to the method set forth above is to first form the complex by reaction of anthranilic acid with silver nitrate and then apply the reaction product by padding a solution or dispersion thereof on the fabric.
The efficiency of the mustard gas barrier is determined by the Dawson Testa measurement of the percent of mustard gas, initially present in an air stream, retained on a fabric after air passage through the fabric. Table I following Example I depicts the relative elfectiveness of the silver derivative of anthranilic acid as compared with anthranilic acid itself and with the copper and iron derivatives; all applied as prescribed in Example I.
EXAMPLE I TABLE I Mustard retention, percent Compound applied 0-2 hrs. 2-4 hrs. 4-6 hrs.
Anthranilic acid 26 Cupric anthranilate 26 Silver anthranilate 98 98 97 Ferric Anthranilate 20 EXAMPLE II To a solution of 27.4 parts (0.20 m.) of anthranilic acid of 99.7% purity in 200 parts by volume of anhydrous 2B alcohol, is added a solution of 34.0 parts of silver nitrate (0.20 m.) in 25 parts by volume of water. The addition is made slowly at 50-55 C. with good stirring. A granular precipitate forms. After stirring for an additional 15 minutes at 50-55 C., the reaction mixture is filtered rapidly while hot and the solid dried overnight at 50-55 C. This crude product consists of 11.2 parts of sparkling light brown crystals which decompose sharply at 160 C. with the immediate formation of a silver mirror. The crude is extracted with 100 parts by volume of boiling anhydrous- 2B alcohol and dried at 5055 C.; 10.6 parts of sparkling gray violet crystals result. These crystals also decompose sharply at C. with the concomitant formation of a silver mirror. Analysis disclosed a product having an empirical formula C H N O Ag The product so formed is applied by padding 9. disper sion of it on the fabric. In a standard test procedure, 60 micrograms of mustard gas treated with 4000 micrograms of the product was completely inactivated.
EXAMPLE III The alcohol filtrate from Example II, when permitted to stand overnight at room temperature deposits 27.8 parts of large light violet crystals. These are purified by dissolving in 250 parts by volume of boiling anhydrous 2B alcohol clarifying with adsorbent charcoal, concentrating the filtrate to a small volume, filtering at room temperature, washing the crystals with alcohol, and drying overnight at 50-55 C. The recrystallized product consists of 14.0 parts of light violet crystals which melt at 155158 C., evolve gas, but dont form a silver mirror. Analysis shows the empirical formula to be CqHqN2O5Ag. The product is applied to the cloth as a dispersion by padding as in Example II. It gives standard test results identical with the product of Example II total inactivation of mustard gas.
While only preferred forms of the invention are shown and described, other forms of the invention are contemplated and numerous changes and modifications may be made therein without departing from the spirit of the in vention as set forth in the appended claims.
What is claimed is:
1. The method of imparting antivesicant properties to an air permeable fabric by treating said fabric with a solution of the reaction product of silver nitrate and anthranilic acid, and drying said fabric.
2. The method set forth in claim 1, wherein said treatment conssts of submerging said fabric in said solution,
and gently squeezing it between rollers prior to drying.
3. The method set forth in claim 1, wherein said anthranilic acid consists of a 20% solution of anthranilic acid in dimethyl formamide and said silver nitrate consists of a 10% aqueous solution.
4. The method of imparting antivesicant properties to an air permeable fabric by treating said fabric with a solution of anthranilic acid, drying and then treating the fabric with a solution of silver nitrate.
5. The method set forth in claim 4 wherein said anthranilic acid consists of a 20% solution of anthranilic acid in dimethyl formamide and said silver nitrate consists of a 10% aqueous solution.
6. The method set forth in claim 4, wherein said treatment consists of soaking said fabric in said acid solution for about one hour, drying said soaked fabric in air at room temperature for about twenty hours, soaking said dried fabric without agitation for about one hour in an excess of said silver nitrate solution and squeezing said fabric gently through rollers.
7. An air permeable fabric vested with antivesicant properties comprising a fabric treated with the reaction products of silver nitrate and anthranilic acid.
References Cited UNITED STATES PATENTS 2,459,896 l/1949 SchWarz 1l7l38.5 2,459,897 1/1949 Schwarz 1l7138.5 2,649,389 8/1953 Williams 117-121 2,885,305 5/1959 Speck 117--121 2,968,579 1/1961 Bullard et al 117121 WILLIAM D. MARTIN, Primary Examiner THEODORE G. DAVIS, Assistant Examiner U.S. Cl. X.R.
US3464847D 1966-10-25 1966-10-25 Treatment of fabrics with anthranilic acid and silver nitrate solutions Expired - Lifetime US3464847A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US58947366A 1966-10-25 1966-10-25

Publications (1)

Publication Number Publication Date
US3464847A true US3464847A (en) 1969-09-02

Family

ID=24358169

Family Applications (1)

Application Number Title Priority Date Filing Date
US3464847D Expired - Lifetime US3464847A (en) 1966-10-25 1966-10-25 Treatment of fabrics with anthranilic acid and silver nitrate solutions

Country Status (1)

Country Link
US (1) US3464847A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4515761A (en) * 1981-07-07 1985-05-07 E. I. Du Pont De Nemours And Company Protective garment or cover, composite semipermeable barrier fabric, and use in detoxification
US6499320B1 (en) 2001-04-03 2002-12-31 Frederick S. Bernhardt Garment having antimicrobial properties and its associated method of manufacture

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2459897A (en) * 1945-07-25 1949-01-25 Schwarz George Silver impregnation
US2459896A (en) * 1945-01-18 1949-01-25 Schwarz George Silver impregnation
US2649389A (en) * 1943-01-16 1953-08-18 Jonathan W Williams Antivesicant compounds and clothing impregnated therewith
US2885305A (en) * 1944-03-13 1959-05-05 Jr John C Speck Polychloro-7, 8-disubstituted-2, 5-diimino glycoluril for use as an antivesicant
US2968579A (en) * 1940-06-19 1961-01-17 Lake Erie Chemical Company Means for protection against vesicants

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2968579A (en) * 1940-06-19 1961-01-17 Lake Erie Chemical Company Means for protection against vesicants
US2649389A (en) * 1943-01-16 1953-08-18 Jonathan W Williams Antivesicant compounds and clothing impregnated therewith
US2885305A (en) * 1944-03-13 1959-05-05 Jr John C Speck Polychloro-7, 8-disubstituted-2, 5-diimino glycoluril for use as an antivesicant
US2459896A (en) * 1945-01-18 1949-01-25 Schwarz George Silver impregnation
US2459897A (en) * 1945-07-25 1949-01-25 Schwarz George Silver impregnation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4515761A (en) * 1981-07-07 1985-05-07 E. I. Du Pont De Nemours And Company Protective garment or cover, composite semipermeable barrier fabric, and use in detoxification
US6499320B1 (en) 2001-04-03 2002-12-31 Frederick S. Bernhardt Garment having antimicrobial properties and its associated method of manufacture

Similar Documents

Publication Publication Date Title
DE2604109A1 (en) ACTIVATION OF HYDRO-SOLUBLE AMINES BY HALOGENS TO CAPTURE RADIOACTIVE IODINE FROM AIRSTREAMS
US3464847A (en) Treatment of fabrics with anthranilic acid and silver nitrate solutions
US2423261A (en) Germicidal product and method of producing same
JPH05117972A (en) Composition for treating textile goods
DE2253976C2 (en) Process for making cellulose-containing fiber materials flame-resistant
DE3032752C2 (en) Process for disinfecting dry cleaning
EP0616071A1 (en) Process for the treatment of fibrous materials with triazin derivatives
US3723058A (en) Removal of free formaldehyde from solutions of methylolated carbamatefinishing agents and textiles treated therewith
DE69535154T2 (en) Process for the treatment of textile materials
US3255078A (en) Process for the treatment of fiber articles of synthetic polyamides and composition produced
US3627476A (en) Amide-glyoxal addition products and their use as crosslinking agents
US2927037A (en) Composition for the destruction of mustard gas
DE1946075B2 (en) METHOD OF MODIFYING CELLULOSE FIBER MATERIALS
US2659681A (en) Gas protective fabric and method of preparing the same
DE2543992C3 (en) Process for cleaning liquid chlorinated hydrocarbons
US3482927A (en) Method for imparting antivesicant properties to fabric
DE1175198B (en) Process for hydrophobing and softening fiber materials
US2885305A (en) Polychloro-7, 8-disubstituted-2, 5-diimino glycoluril for use as an antivesicant
US3794466A (en) Single bath chromic chloride mineral dyeing process for cellulosics
US2926107A (en) Cloth containing antivesicant
US1923223A (en) Mothproofing substances
US3403969A (en) Solvent bonding of fiber fleeces including shock-like heat treatment prior to complete vaporization of solvent
US1748579A (en) Mothproofing material
US2968579A (en) Means for protection against vesicants
JPS58109577A (en) Flameproofing agent composition