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US3650819A - Durable fire-retardant finish for cellulosic textile materials - Google Patents

Durable fire-retardant finish for cellulosic textile materials Download PDF

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US3650819A
US3650819A US765961A US3650819DA US3650819A US 3650819 A US3650819 A US 3650819A US 765961 A US765961 A US 765961A US 3650819D A US3650819D A US 3650819DA US 3650819 A US3650819 A US 3650819A
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Prior art keywords
aziridinyl
phosphine oxide
finish
fabric
percent
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US765961A
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Robert George Weyker
George Louis Mina
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Wyeth Holdings LLC
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American Cyanamid Co
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Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating 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
    • D06M13/487—Aziridinylphosphines; Aziridinylphosphine-oxides or sulfides; Carbonylaziridinyl or carbonylbisaziridinyl compounds; Sulfonylaziridinyl or sulfonylbisaziridinyl compounds
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913—Rod, strand, filament or fiber
    • Y10T428/2933—Coated or with bond, impregnation or core
    • Y10T428/2964—Artificial fiber or filament
    • Y10T428/2965—Cellulosic
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913—Rod, strand, filament or fiber
    • Y10T428/2933—Coated or with bond, impregnation or core
    • Y10T428/2971—Impregnation
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31971—Of carbohydrate
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20—Coated 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
    • Y10T442/2631—Coating or impregnation provides heat or fire protection
    • Y10T442/2672—Phosphorus containing
    • Y10T442/268—Phosphorus and nitrogen containing compound

Definitions

  • R4 R: 0 ,1, R and R are hydrogen or lower alkyl; and R, and R are alkyl, or, taken together with the nitrogen, represent a heterocyclic ring, followed by a curing step.
  • This invention relates to fire-retardant finishes for textile materials. More particularly, it relates to amethod for improving the wash fastness for a cyanamide-phosphoric acidfire-retardant finish for cellulosic textile materials;
  • the cyanamide-phosphoric acid finish(Pyroset CP, of AmericanCyanamid Co.) of U.S.- Pat. 2,530,261 imparts very good fire-retardant properties-to cellulosic textile materials.
  • the finish however, suffers frompoor durability to laundering when hard water is used.
  • the wash fastnes'swithsofv water is good.
  • the loss in fire retardancy due tolaundering in hardwater is believed to be due to an ion exchange, i.e., base' exchange, with ammonium ion replaced by calcium. Analysis shows a decrease in nitrogen content and an-increase in calcium con tent of the fabric as the washingsin'hard water are repeated. Also, the rate of loss of fire retardancy increases as the hardness of the wash water increases. lonexchange with sodium ions is much slower than withcalcium ions. This explains why the fire retardancy is more durable to washing withsoft water, or with hard water plus Calgon or. a sequestering agent. Other metal ions are also harmful, zinc ions having been shown to be more harmful than calcium ions.
  • R and R are hydrogen or loweralkyl; and R and R,- are alkyl, or, taken together with the nitrogen, represent a heterocyclic ring, followed by a curing step.
  • Compounds of Formula I include bis(laziridinyl)al-' kylphosphine oxides, such as bis( l-aziridinyl)ethylphosphine oxide, bis(1-aziridinyl)butylphosphine.
  • bis(laziridinyl)-arylphosphine oxides such as bis(l-aziridinyl)phenylphosphine oxide, bis( l aziridinyl)-p tolyphosphine oxide, bis(1-aziridinyl) p-chlorophenylphosphine oxide, bis(l-aziridinyl)-2-naphthylphosphine oxide, etc.
  • bis(laziridinyl)cycloalkylphosphine oxides such as bis(l-aziridinyl)cyclohexylphosphine oxide, etc.
  • bis(l-aziridinyDdisubstituted-aminophosphine oxides such as bis(l-aziridinyl)(dibutylamino)phosphine oxide, bis(1-aziridinyl)(dioctylamino)phosphine oxide, bis
  • the aziridinyl phosphine oxides of Formula I can be prepared by the procedures described in U.S. Pat. Nos. 2,606,900; 2,606,902; 2,654,738 and 2,663,705.
  • the temperature of the aqueous solution of cyanamide and phosphoric acid is preferably at about l0'20 C. or below, and not over 30 C.
  • the fabric After the fabric has been treated with the aqueous solution of cyanamide and phosphoric acid, it is dried by any convenient method, as in an oven at -105 C., and is then heated at an elevated temperature to effect a cure of the finish on the textile material.
  • a temperature between C. and 200 C., preferably between C. and 175 C., is employed for the curing operation depending on fabric weight.
  • the time required is betweenabout l and 20 minutes, depending on the temperature used and fabric weight.
  • the drying step can be omitted and cure times extended slightly to accomplish drying and curing in one operation.
  • Tl'ie textile material should containatleast 50 percent cellulosic fibers. It can be in the form ofa woven or knitted fabric, nonwoven fabric, yarns, etc.
  • the aziridinyl phosphine oxide is applied to the textile material bearing the cured cyanamide-phosphoric acid from a suitable solvent medium using any conventional procedure such as by padding, dipping, spraying, etc.
  • a suitable solvent medium such as by padding, dipping, spraying, etc.
  • the aziridinyl compound is sufficiently soluble in water, it is advantageous tousean aqueous solution of the compound.
  • an inert solvent such as chlorinated hydrocarbons and glycol ethers can be used.
  • the amount of aziridinyl phosphine oxide used should be between 1 percent and 25 percent, preferably between 5 percent and 20 percent, based on the weight of the textile material.
  • the temperature of the solution of aziridinyl compound is preferably at'about room temperature, but it can be higher or lower within practical limits.
  • the treated textile material is dried by any convenient method, as in an oven at 105 C., and is then heated at an elevated temperature to effect a cure" of the aziridinyl phosphine oxide finish on the textile material.
  • a temperature between 105 C. and 200 C., preferably between 125 C. and C., is recommended for the curing operation.
  • the time required is between about 1 and 5 minutes, depending on the temperature used and weight of the fabric. If desired, the drying and curing operation can be done in one operation.
  • the aziridinyl phosphine oxide treatment not only improves the durability of the cyanamide-phosphoric acid fire-retardant finish, but it also increases the wrinkle recovery properties of the fabric, thus providing the fabric with durable wash and wear properties.
  • EXAMPLE I A. Treatment of Fabric with Cyanamide and Phosphoric Acid A pad bath was prepared by mixing 1,200 g. of 50 percent aqueous cyanamide solution, 328 g. of ice and 472 g. of 85 percent phosphoric acid. The bath was padded onto 80 X 80 cotton percale obtaining an 80 percent wet pickup. The treated fabric was dried, and the finish was cured by heating the fabric at 150 C. for 3 minutes.
  • the durability of the fire-retardant finish to laundering was determined by repeatedly washing the fabric in an automatic washing machine using hard water, the water having a calcium ion content of about 70 p.p.m. After each washing operation, the fire resistance of the fabric was determined by a vertical flame test according to Standard Test Method AATCC 34-l966. The washings and flame testing were continued as long as the char length of the burned fabric was less than 6 inches. The limit of wash durability was reached when the char length was 6 inches.
  • the fire resistance of the fabric obtained by Treatment A plus B was durable for about 40 launderings in hard water.
  • the fire resistance of the fabric from Treatment A alone was durable for about five launderings in hard water.
  • EXAMPLE II A series of aqueous solutions containing 2.5 percent, percent, 7.5 percent, 10 percent, percent and percent of tris(1-aziridinyl)phosphine oxide (APO) were padded onto 80 X 80 cotton percale which had been treated with cyanamide and phosphoric acid according to the procedure of Example I. A wet pickup of about 80 percent was obtained. The treated fabrics were dried and cured at 125 C. for 3 minutes.
  • APO tris(1-aziridinyl)phosphine oxide
  • the durability of the fire-retardant finishes to laundering in hard water was determined by the procedure of Example I.
  • the wrinkle recovery of the treated fabrics was measured by Tentative Test Method AATCC 66-1959T after 30 washes.
  • the fabric treated only with cyanamide and phosphoric acid had a wrinkle recovery of about 230C.
  • EXAMPLE 111 A Treatment of Fabric with Cyanamide and Phosphoric Acid The procedure of Part A of Example I was followed with the exception that the finish was cured by heating the fabric at 150 C. for 5 minutes and the fabric was not rinsed in water after the curing step.
  • a method for improving the durability of a cyanamidephosphoric acid fire-retardant textile finish on a cellulosic textile material comprising impregnating the textile material containing the cyanamide phosphoric acid finish with an aziridinyl phosphine oxide of the formula:
  • R, and R are hydrogen or lower alkyl; and R and R. are alkyl or, taken together with the nitrogen, represent a heterocyclic ring, and heating the textile finish at a temperature between C. and 200 C.
  • aziridinyl phosphine oxide is tris( l-aziridinyl)phosphine oxide.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Fireproofing Substances (AREA)

Abstract

WHEREIN R is alkyl, aryl, cyclo alkyl, R1 and R2 are hydrogen or lower alkyl; and R3 and R4 are alkyl, or, taken together with the nitrogen, represent a heterocyclic ring, followed by a curing step.

A method for providing a hard water wash durable cyanamidephosphoric acid, flame-retardant finish for cellulosic textile materials which comprises aftertreating the textile material bearing the cyanamide-phosphoric acid finish with an aziridinyl phosphine oxide of the formula:

Description

United States Patent Weyker et al.
[ 1 Mar.21, 1972 [54] DURABLE FIRE-RETARDANT FINISH FOR CELLULOSIC TEXTILE MATERIALS [72] Inventors: Robert George Weyker, North Plaintield; George Louis Mina, Highbridge, both of [211 App]. No.: 765,961
[52] U.S. C1 ..ll7/l36,117/137,117/139.4, 1 17/143 R [51] Int. Cl ..C09k 3/28, D06m 13/26 [58] Fleld of Search ..117/136,139.4, 143 R, 76 T, 117/62, 63
[56] References Cited UNITED STATES PATENTS 2,454,245 ll/1948 Woodruff ..l17/76 UX 2,470,042 11/1946 McLean et a1. ....117/76 UX 2,494,391 [/1950 Johnson et a1. ..117/76 X 2,530,261 11/1950 Morton et a1. 117/137 X 2,640,000 5/1953 Seyb et a1. ..l17/76 2,870,042 1/1959 Chance et al.... .117/136 2,891,877 6/1959 Chance et a1.... 17/136 2,901,444 8/1959 Chance et a1. 17/136 X 2,906,592 9/1959 Reeves et a1, 17/136 X 2,911,325 11/1959 Drake et a1. ..117/136 3,034,919 5/1962 Steinhauer ..117/143 X FOREIGN PATENTS OR APPLICATIONS 654,627 12/1962 Canada ..1l7/l36 OTHER PUBLICATIONS Drake et a1., imparting Crease Resistance," Textile Research Journal, Vol. 29, No. 2, pps. 155- 164, Feb., 1959.
Primary Examiner-Wi1liam D. Martin Assistant Examiner-Harry J. Gwinnell Attorney-Charles J. Fickey [57] ABSTRACT wherein R is alkyl, aryl, cyclo alkyl,
R: on,
R4 R: 0 ,1, R and R are hydrogen or lower alkyl; and R, and R are alkyl, or, taken together with the nitrogen, represent a heterocyclic ring, followed by a curing step.
6 Claims, No Drawings DURABLE FlRE-RETARDANT FINISH FOR CELLULOSIC TEXTILE MATERIALS This invention relates to fire-retardant finishes for textile materials. More particularly, it relates to amethod for improving the wash fastness for a cyanamide-phosphoric acidfire-retardant finish for cellulosic textile materials;
The cyanamide-phosphoric acid finish(Pyroset CP, of AmericanCyanamid Co.) of U.S.- Pat. 2,530,261 imparts very good fire-retardant properties-to cellulosic textile materials.
The finish, however, suffers frompoor durability to laundering when hard water is used. The wash fastnes'swithsofv water is good.
There is moderate improvement washingin'hard water when sodium hexametaphosphate Calgon," ofl-lagan Chemicals & Controls, Inc.) is used in the hard wash water. A slight improvement is found when a sequestering agent, such as the sodium salt of ethylenediamine-tetracetic acid, is used in the hard water.
The loss in fire retardancy due tolaundering in hardwater is believed to be due to an ion exchange, i.e., base' exchange, with ammonium ion replaced by calcium. Analysis shows a decrease in nitrogen content and an-increase in calcium con tent of the fabric as the washingsin'hard water are repeated. Also, the rate of loss of fire retardancy increases as the hardness of the wash water increases. lonexchange with sodium ions is much slower than withcalcium ions. This explains why the fire retardancy is more durable to washing withsoft water, or with hard water plus Calgon or. a sequestering agent. Other metal ions are also harmful, zinc ions having been shown to be more harmful than calcium ions.
It has now been discovered that the wash durability in hard water of the cyanamide-phosphoric acid textile finish can be greatly improved by aftertreating the textile material bearing the cyanamide-phosphoric acid finish withan-aziridinyl phosphine oxide ofFormula 1:
R and R are hydrogen or loweralkyl; and R and R,- are alkyl, or, taken together with the nitrogen, represent a heterocyclic ring, followed by a curing step.
Compounds of Formula I include bis(laziridinyl)al-' kylphosphine oxides, such as bis( l-aziridinyl)ethylphosphine oxide, bis(1-aziridinyl)butylphosphine. oxide, etc.; bis(laziridinyl)-arylphosphine oxides, such as bis(l-aziridinyl)phenylphosphine oxide, bis( l aziridinyl)-p tolyphosphine oxide, bis(1-aziridinyl) p-chlorophenylphosphine oxide, bis(l-aziridinyl)-2-naphthylphosphine oxide, etc.; bis(laziridinyl)cycloalkylphosphine oxides, such as bis(l-aziridinyl)cyclohexylphosphine oxide, etc.; bis(l-aziridinyDdisubstituted-aminophosphine oxides, such as bis(l-aziridinyl)(dibutylamino)phosphine oxide, bis(1-aziridinyl)(dioctylamino)phosphine oxide, bis(l-aziridinyl)piperidinophosphine oxide, bis(l-aziridinyl)morpholinophosphine oxide, bis(2methy1-1-aziridinyl)piperidinophosphine oxide, bis(2,2- dimethyl-l-aziridinyl)piperidinophosphine oxide, etc.; and tris-(l-aziridinyl)phosphine oxides, such as tris(1 aziridinyl)phosphine oxide itself, tris(Z-methyl-l-aziridinyl)phosphine oxide, tris(2,2-dimethyl-l aziridinyhphosphine oxide, etc. The preferred polyazirldinyl phosphine oxide is tris(laziridinyl)phosphineoxide'of Formula ll:
in durability ofthe finish'to" Formula II The aziridinyl phosphine oxides of Formula I can be prepared by the procedures described in U.S. Pat. Nos. 2,606,900; 2,606,902; 2,654,738 and 2,663,705.
The procedure for applying the cyanamide-phosphoric acid is described in-U.S. Pat. No. 2,530,261. Our results indicate thatat least 10 percent to 30- percent, preferably at least 20 percent, of cyanamide, and at least 5 percent to 25 percent, preferably at least 15 percent, of phosphoric acid (H PO should be appliedto'the textile material. The percentages are based on the weight of the material. It is advantageous to apply the twoagents simultaneously from aqueous solution by any of the procedures conventionally used to apply aqueous textile finishes, such as by. padding, dipping, spraying, etc.
The temperature of the aqueous solution of cyanamide and phosphoric acid is preferably at about l0'20 C. or below, and not over 30 C.
After the fabric has been treated with the aqueous solution of cyanamide and phosphoric acid, it is dried by any convenient method, as in an oven at -105 C., and is then heated at an elevated temperature to effect a cure of the finish on the textile material. A temperature between C. and 200 C., preferably between C. and 175 C., is employed for the curing operation depending on fabric weight. The time required is betweenabout l and 20 minutes, depending on the temperature used and fabric weight. Alternatively, the drying step can be omitted and cure times extended slightly to accomplish drying and curing in one operation.
' Tl'ie textile material should containatleast 50 percent cellulosic fibers. It can be in the form ofa woven or knitted fabric, nonwoven fabric, yarns, etc.
The aziridinyl phosphine oxide is applied to the textile material bearing the cured cyanamide-phosphoric acid from a suitable solvent medium using any conventional procedure such as by padding, dipping, spraying, etc. Where the aziridinyl compound is sufficiently soluble in water, it is advantageous tousean aqueous solution of the compound. This particularly applies to the preferred compound, tris( l-aziridinyl)phosphine oxide ofFormula 11. When the compound is not sufficiently soluble in water, an inert solvent such as chlorinated hydrocarbons and glycol ethers can be used.
The amount of aziridinyl phosphine oxide used should be between 1 percent and 25 percent, preferably between 5 percent and 20 percent, based on the weight of the textile material.
The temperature of the solution of aziridinyl compound is preferably at'about room temperature, but it can be higher or lower within practical limits.
The treated textile material is dried by any convenient method, as in an oven at 105 C., and is then heated at an elevated temperature to effect a cure" of the aziridinyl phosphine oxide finish on the textile material. A temperature between 105 C. and 200 C., preferably between 125 C. and C., is recommended for the curing operation. The time required is between about 1 and 5 minutes, depending on the temperature used and weight of the fabric. If desired, the drying and curing operation can be done in one operation.
Before applying the aziridinyl phosphine oxide it is desirable to rinse the cyanamide-phosphoric acid treated textile material in water. This procedure removes phosphoric acid and increases the effectiveness of the aziridinyl compound.
The aziridinyl phosphine oxide treatment not only improves the durability of the cyanamide-phosphoric acid fire-retardant finish, but it also increases the wrinkle recovery properties of the fabric, thus providing the fabric with durable wash and wear properties.
The following specific examples are given to illustrate the invention and are not intended to be limitative.
EXAMPLE I A. Treatment of Fabric with Cyanamide and Phosphoric Acid A pad bath was prepared by mixing 1,200 g. of 50 percent aqueous cyanamide solution, 328 g. of ice and 472 g. of 85 percent phosphoric acid. The bath was padded onto 80 X 80 cotton percale obtaining an 80 percent wet pickup. The treated fabric was dried, and the finish was cured by heating the fabric at 150 C. for 3 minutes.
B. Treatment of Fabric with Tris( l-aziridinyl)phosphine Oxide A 10 percent aqueous solution of tris( l-aziridinyl)phosphine oxide was padded onto the fabric from Treatment A obtaining an 80 percent wet pickup. The treated fabric was dried and the finish was cured by heating the fabric at 125C. for 3 minutes.
The durability of the fire-retardant finish to laundering was determined by repeatedly washing the fabric in an automatic washing machine using hard water, the water having a calcium ion content of about 70 p.p.m. After each washing operation, the fire resistance of the fabric was determined by a vertical flame test according to Standard Test Method AATCC 34-l966. The washings and flame testing were continued as long as the char length of the burned fabric was less than 6 inches. The limit of wash durability was reached when the char length was 6 inches.
The fire resistance of the fabric obtained by Treatment A plus B was durable for about 40 launderings in hard water. For comparison, the fire resistance of the fabric from Treatment A alone was durable for about five launderings in hard water.
EXAMPLE II A series of aqueous solutions containing 2.5 percent, percent, 7.5 percent, 10 percent, percent and percent of tris(1-aziridinyl)phosphine oxide (APO) were padded onto 80 X 80 cotton percale which had been treated with cyanamide and phosphoric acid according to the procedure of Example I. A wet pickup of about 80 percent was obtained. The treated fabrics were dried and cured at 125 C. for 3 minutes.
The durability of the fire-retardant finishes to laundering in hard water was determined by the procedure of Example I.
The wrinkle recovery of the treated fabrics was measured by Tentative Test Method AATCC 66-1959T after 30 washes.
The results are shown in Table I.
The fabric treated only with cyanamide and phosphoric acid had a wrinkle recovery of about 230C.
EXAMPLE 111 A. Treatment of Fabric with Cyanamide and Phosphoric Acid The procedure of Part A of Example I was followed with the exception that the finish was cured by heating the fabric at 150 C. for 5 minutes and the fabric was not rinsed in water after the curing step.
B. Treatment of Fabric with Tris( l-aziridinyl)phosphine Oxide The procedure of Part B of Example I was followed with the exception that the finish was cured by heating the fabric at 150 C. for 5 minutes.
The durability of the fire-resistant finishes of Treatment A and A B were determined by the procedure of Example I. The results are shown in Table 11.
TABLE ll Treatment Durability of Finish A 2 washes A B 9-12 washes While certain specific embodiments and preferred modes of practice of the invention have been set forth, it will be understood that this is solely for purposes of illustrating the invention, and that various changes and modifications may be made without departing from the spirit of the disclosure or the scope of the appended claims.
We claim:
1. A method for improving the durability of a cyanamidephosphoric acid fire-retardant textile finish on a cellulosic textile material comprising impregnating the textile material containing the cyanamide phosphoric acid finish with an aziridinyl phosphine oxide of the formula:
R, and R are hydrogen or lower alkyl; and R and R. are alkyl or, taken together with the nitrogen, represent a heterocyclic ring, and heating the textile finish at a temperature between C. and 200 C.
2. The method of claim 1 where the aziridinyl phosphine oxide is tris( l-aziridinyl)phosphine oxide.
3. The method of claim 1 wherein said aziridinyl phosphine oxide is employed as an aqueous solution.
4. The method of claim 1 wherein said aziridinyl phosphine oxide is employed in an inert organic solvent.
5. The method of claim 1, including a water rinse prior to said impregnation with said aziridinyl phosphine oxide.
6. Cellulosic textile materials treated by the method of claim 1.

Claims (5)

  1. 2. The method of claim 1 where the aziridinyl phosphine oxide is tris(1-aziridinyl)phosphine oxide.
  2. 3. The method of claim 1 wherein said aziridinyl phosphine oxide is employed as an aqueous solution.
  3. 4. The method of claim 1 wherein said aziridinyl phosphine oxide is employed in an inert organic solvent.
  4. 5. The method of claim 1, including a water rinse prior to said impregnation with said aziridinyl phosphine oxide.
  5. 6. Cellulosic textile materials treated by the method of claim
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US3997699A (en) * 1975-04-25 1976-12-14 Ethyl Corporation Flame resistant substrates
US20100233925A1 (en) * 2006-03-03 2010-09-16 Perachem Limited Composition and Method

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US2494391A (en) * 1947-05-28 1950-01-10 Du Pont Fire-resistant opaque window shade material and process of making same
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US2640000A (en) * 1947-06-07 1953-05-26 Diamond Alkali Co Flameproofing method and product
US2870042A (en) * 1956-06-05 1959-01-20 Leon H Chance Flame resistant organic textiles and method of production
US2891877A (en) * 1956-06-05 1959-06-23 Leon H Chance Flame resistant organic textiles and method of production
US2901444A (en) * 1956-06-05 1959-08-25 Leon H Chance Polymers made from 1-aziridinyl phosphine oxides and sulfides and flame resistant organic textiles
US2906592A (en) * 1957-08-20 1959-09-29 Wilson A Reeves Flame- and crease-resistant textiles from aziridine carboxyalkylcellulose
US2911325A (en) * 1956-06-05 1959-11-03 Jr George L Drake Flame resistant organic textiles and method of production
US3034919A (en) * 1960-03-18 1962-05-15 Stauffer Chemical Co Fire retardant composition and cellulosic fabric treated therewith
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3997699A (en) * 1975-04-25 1976-12-14 Ethyl Corporation Flame resistant substrates
US20100233925A1 (en) * 2006-03-03 2010-09-16 Perachem Limited Composition and Method
US8853106B2 (en) 2006-03-03 2014-10-07 Perachem Limited Phosphorus-contaning flame-retardant compositions

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