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US2580286A - Process of treating cellulosic and similar materials - Google Patents

Process of treating cellulosic and similar materials Download PDF

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Publication number
US2580286A
US2580286A US713926A US71392646A US2580286A US 2580286 A US2580286 A US 2580286A US 713926 A US713926 A US 713926A US 71392646 A US71392646 A US 71392646A US 2580286 A US2580286 A US 2580286A
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materials
acid
cellulose
phosphate
degradation
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US713926A
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Rowell R Dorsett
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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
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/68Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof
    • D06M11/72Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof with metaphosphoric acids or their salts; with polyphosphoric acids or their salts; with perphosphoric acids or their salts

Definitions

  • This invention relatesto a process of treating.
  • cellulosic materials or materials similar ,i'n nature orv composition to the cellulosic materials, such as starches, esters ,of cellulose, or regener ated cellulose materials, to render them, resistant to degradation by the action of, acids and ,un--- stable chlorinated compounds which .yieldacid when subjected to conditions of temperature and/or high humidities.
  • chlorinated parafiins, tetrachloroethane, and products 'of'the general structure RN-CN:R a t 1 where R is an alkyl group are typical examples of unstable chlorinated compounds which .react in this manner.
  • the cellulosic .materials herein referred to could be textiles made from cotton, linen, jute, ramie, or regenerated cellulose, materials made from wood pulp such as paper, and materials made of modifiedcell-ulose such as cellulose acetate, nitrocellulose, etc.
  • the cellulosic materials, or materials similar in nature to cellulose, when treated with highly chlorinated compounds will degrade or hydrolyze when exposed to heat and moisture. These materials are readily degraded by acid in solution or acid formed from the breakdown of unstable chlorinated compounds which have been used to treat the cellulose materials.
  • the action of the acid in either case is to convert the cellulose .to a weaker hydro-cellulose, thus tendering or weakening the fiber.
  • the degree to whichften- .derlng will take place depends to a large extent upon the temperature at which drying is effected, as well as the humidity conditions prevalent during exposure to the drying temperatures. Cotton which has been tenderedby acid has undergone chemical change, evidenced by a slight increase in'the percentage ofhydrogenand oxygen.
  • This product formed bythe'action of acid on cellulose is known as hydro-cellulose.
  • the extent of this degradation of cellulose depends on the temperature, the concentration of the acid formed, and the length of time such cellulosic materials are exposed to the action of the acid. Degradation implies the zim pairment and even the destruction of the strength of cellulosic materials. I have observed an appreciable loss in the tensile strength of a cotton fabric thoroughly wetted in certain'acid 5 solutions and dried.
  • An object of this invention is to provide a process for treating cellulosic materials or materials of a similar nature to inhibit the degradation thereof when subjected to the action of acids, as, for example, hydrochloric, sulphuric, phosphoric or oxalicacid, or compounds which break down to form any oneof these acids.
  • a further object of the invention is to provide a. processfor treating fabrics such as cotton or other cellulosic fabrics, whether or not such fabrics have been treated or sized with resins, starches or other materials so that when such fabrics are exposed to acid in solution, the fabrics will be rendered partially or totally immune to attack by such acid agents.
  • alkali-metal molecularly dehydrated phosphate such as. the water soluble sodium, potassium, lithium, and ammonium phosphate glasses or the crystalline tetrasodium pyrophosphate and sodium tripolyphosphate.
  • alkali-metal phosphate glasses may be generally designated by the formula where .M is an 'alkali-metal or the ammonium radical, and X is a, number ranging from zero to two.
  • the alkali-metal phosphate glasses may be'prepared over a wide range of composition as indicated by a ratio of M2O:P2O5 of from less than 0.8:1 to about 1.7:1.
  • the broad range of this ratio extends from glassy P205 where the ratio of MzOtPzOs is 0, to a ratio of 2:1 which is that of the pyrophosphate composition.
  • the cellulosic materials may be impregnated in a solution containing a molecularly dehydrated phosphate before such materials have been exposed to the action of the aforementioned acid degrading agents.
  • the solutions should have a concentration of at least 0.5% of molecularly dehydrated phosphate, but may contain as high as 2% or 3%.
  • a solution containing a concentration of l of molecularly dehydrated phosphate, such asa sodium; phosphate glass having a ratio of Na2O:PzO5 of about 1.1:1 willproduce very good protective results when measured by the tensile strength of the cellulose fabric after action of acid agents which normally cause degradation.
  • I may also utilize the invention by immersing the cellulosic materials inan aqueous solution containing about from 0.5% to about 3% of a molecularly dehydrated phosphate followed by removing the materials from the solution and drying them, when drying is practicable. After above described.
  • the cellulosic materials have been treated in a solution of molecularly dehydrated phosphate, I prefer, as above stated, that the material be dried after removal from such solution. However, I have found that even though not dried, these materials are protected Instead of first treating the cellulosic materials 1 in a solution containing a molecularly dehydrated phosphate, Inlay treat such materials in a solution containing both acid or acid-forming compounds and niolecularly dehydrated phosphate. When a mixture of the molecularly dehydrated phosphate and acid are used, the amount of molecularly dehydrated phosphate in the mixture with relation to the solution should be such as to provide a concentration of at least 0.5%.
  • the proportions of phosphate to acid-liberating product may vary from about 2:1 to about 20:1. If such a mixture, when added to water, produces an acid concentration of 0.50%, the contration of phosphate would be 1.0% for the 2:1 ratio mixture and for :1 ratio mixture.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Paper (AREA)

Description

Patented Dec. 25, 1951 2,580,286 ICE PROCESS or TREATINGLCELLULOSIC AND MATERIALS ."Rnwl i om Ba mo M No Drawing.
Application= December 4, 1946, Serial N o. 71.31926 '3 cl i in -138.5
This invention relatesto a process of treating.
cellulosic materials, or materials similar ,i'n nature orv composition to the cellulosic materials, such as starches, esters ,of cellulose, or regener ated cellulose materials, to render them, resistant to degradation by the action of, acids and ,un--- stable chlorinated compounds which .yieldacid when subjected to conditions of temperature and/or high humidities. "Chlorinated parafiins, tetrachloroethane, and products 'of'the general structure RN-CN:R a t 1 where R is an alkyl group, are typical examples of unstable chlorinated compounds which .react in this manner. I
This applicationis a continuation-in-part of my copending application, Serial No. 591,428, filed May 1, 1945, which is nowabandoned.
The cellulosic .materials herein referred to could be textiles made from cotton, linen, jute, ramie, or regenerated cellulose, materials made from wood pulp such as paper, and materials made of modifiedcell-ulose such as cellulose acetate, nitrocellulose, etc.
The cellulosic materials, or materials similar in nature to cellulose, when treated with highly chlorinated compounds will degrade or hydrolyze when exposed to heat and moisture. These materials are readily degraded by acid in solution or acid formed from the breakdown of unstable chlorinated compounds which have been used to treat the cellulose materials. The action of the acid in either case is to convert the cellulose .to a weaker hydro-cellulose, thus tendering or weakening the fiber. The degree to whichften- .derlng will take place depends to a large extent upon the temperature at which drying is effected, as well as the humidity conditions prevalent during exposure to the drying temperatures. Cotton which has been tenderedby acid has undergone chemical change, evidenced by a slight increase in'the percentage ofhydrogenand oxygen. This product formed bythe'action of acid on cellulose is known as hydro-cellulose. The extent of this degradation of cellulose depends on the temperature, the concentration of the acid formed, and the length of time such cellulosic materials are exposed to the action of the acid. Degradation implies the zim pairment and even the destruction of the strength of cellulosic materials. I have observed an appreciable loss in the tensile strength of a cotton fabric thoroughly wetted in certain'acid 5 solutions and dried.
An object of this invention is to provide a process for treating cellulosic materials or materials of a similar nature to inhibit the degradation thereof when subjected to the action of acids, as, for example, hydrochloric, sulphuric, phosphoric or oxalicacid, or compounds which break down to form any oneof these acids. 'An
example of such acompound is .a highly chlo-,
A further object of the invention is to provide a. processfor treating fabrics such as cotton or other cellulosic fabrics, whether or not such fabrics have been treated or sized with resins, starches or other materials so that when such fabrics are exposed to acid in solution, the fabrics will be rendered partially or totally immune to attack by such acid agents.
I have found that cellulosic materials or other materials of a similar nature or composition may be protected against degradation by treating with an aqueous solution containing alkali-metal molecularly dehydrated phosphate, such as. the water soluble sodium, potassium, lithium, and ammonium phosphate glasses or the crystalline tetrasodium pyrophosphate and sodium tripolyphosphate. The alkali-metal phosphate glasses may be generally designated by the formula where .M is an 'alkali-metal or the ammonium radical, and X is a, number ranging from zero to two. The alkali-metal phosphate glasses may be'prepared over a wide range of composition as indicated by a ratio of M2O:P2O5 of from less than 0.8:1 to about 1.7:1. The broad range of this ratio extends from glassy P205 where the ratio of MzOtPzOs is 0, to a ratio of 2:1 which is that of the pyrophosphate composition.
This invention may be practiced or applied in various procedures. For example, the cellulosic materials may be impregnated in a solution containing a molecularly dehydrated phosphate before such materials have been exposed to the action of the aforementioned acid degrading agents. The solutions should have a concentration of at least 0.5% of molecularly dehydrated phosphate, but may contain as high as 2% or 3%. I have found that a solution containing a concentration of l of molecularly dehydrated phosphate, such asa sodium; phosphate glass having a ratio of Na2O:PzO5 of about 1.1:1, willproduce very good protective results when measured by the tensile strength of the cellulose fabric after action of acid agents which normally cause degradation.
I may also utilize the invention by immersing the cellulosic materials inan aqueous solution containing about from 0.5% to about 3% of a molecularly dehydrated phosphate followed by removing the materials from the solution and drying them, when drying is practicable. After above described. When the cellulosic materials have been treated in a solution of molecularly dehydrated phosphate, I prefer, as above stated, that the material be dried after removal from such solution. However, I have found that even though not dried, these materials are protected Instead of first treating the cellulosic materials 1 in a solution containing a molecularly dehydrated phosphate, Inlay treat such materials in a solution containing both acid or acid-forming compounds and niolecularly dehydrated phosphate. When a mixture of the molecularly dehydrated phosphate and acid are used, the amount of molecularly dehydrated phosphate in the mixture with relation to the solution should be such as to provide a concentration of at least 0.5%.
When mixtures of molecularly dehydrated phosphates and unstable compounds which liberate acid under favorable conditions are employed, the proportions of phosphate to acid-liberating product may vary from about 2:1 to about 20:1. If such a mixture, when added to water, produces an acid concentration of 0.50%, the contration of phosphate would be 1.0% for the 2:1 ratio mixture and for :1 ratio mixture.
An example of my process is whereI treated a cotton broadcloth material that had-been prop- H erly bottomed by the progressive Jig process (desizing and caustic boil) in a solution of 0.5% hydrochloric acid. The goods were removed from this solution and allowed to dry in the air. At
the end of eight hours the cloth was dry and par- 1 tial degradation of the cellulose had taken place. Another piece of the same broadcloth was passed through an aqueous solution containing 0.5% hydrochloric acid and 1% sodium phosphate glass, the glass having a ratio composition of NazOzPzOs about 1.1:1. After removal from this solution, the cloth was dried. Very little degradation of the second piece of fabric was noticed.
The following table will show the benefits derived from the addition of molecularly dehydrated phosphate to an acid solution to inhibit the degradation of cellulose treated in such solutions:
Tensile Strength (ill/in!) Amd Solution Treated at 100% Air Dried relative humidity at 70 0. for 19 hrs.
Control 75. 4 62. 0 0.25% HzSO4 48. 6 9. 9 0.25% HzSO4+0.5% phosphate. 55. 3 24. 7 0.25% H2804+1.O% phosphate. 59. 1 32. 8 0.25% E01 46. 7 21. 2 0.25% HCl-i-l.0% phosphate 58. 2 50.0
fabrics exposed to the severe climatic conditions of humidity at elevated temperatures.
Having thus described the invention, what I claim as new and desire to secure by Letters Patentis:
I claim:
1. The method of treating materials of the class consisting of cellulose, cellulose coated with resins, cellulose coated with starch, and cellulose coated with mixtures of resins and starch to thereby inhibit degradation thereof when contacted with acid which consists in wetting said materials with an aqueous solution containing from about 0.5% by weight to about 10.0% by weight of an alkali-metal molecularly dehydrated glassy phosphate having a molar ratio of M20 to P205 of from about 0.811- to 1.7 :1, where M is a member of the group consisting of ammonium, lithium, sodium and potassium, removing said materials from contact with said solution and drying the same, the phosphate retained by said materials inhibiting degradation thereof when wetted with acid.
2. The method of treating materials of the class consisting of cellulose, cellulose coated with resins, cellulose coated with starch, and cellulose coated with mixtures of resins and starch to thereby inhibit degradation thereof when contacted with acid which consists in wetting said materials with an aqueous solution containing from about 0.5% by weight to about 10.0% by weight of an alkali-metal molecularly dehydrated glassy phosphate having a molar ratio of M20 to P205 of from about 0.821 to 1.311, where M is a member of the group consisting of ammonium, lithium, sodium and potassium, removing said materials from contact with said solution and drying the same, the phosphate retained by said materials inhibiting degradation thereof when wetted with acid.
3. The method of treating materials of the class consisting of cellulose, cellulose coated with resins, cellulose coated with starch, and cellulose coated with mixtures of resins and starch to thereby inhibit degradation thereof when contacted with acid which consists in wetting said materials with an aqueous solution containing from about 0.5% by weight to about 10.0% by weight of an alkali-metal molecularly dehydrated phosphate having a molar ratio of alkali-metal oxide to phosphorus pentoxide (P205) of from about 0.8:1 to 2:1, the alkali-metal of said alkalimetal oxide being selected from the group consisting of sodium, potassium, lithium and ammonium, removing said materials from contact with said solution and drying the same, the phosphate retained by said materials inhibiting degradation thereof when wetted with acid.
ROWELL R. DORSETT.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Dreyfus et al May 28, 1940

Claims (1)

1. THE METHOD OF TREATING MATERIAL OF THE CLASS CONSISTING OF CELLULOSE, CELLULOSE COATED WITH RESIN, CELLULOSE COATED WITH STARCH, AND CELLULOSE COATED WITH MIXTURES OF RESIN AND STARCH TO THEREBY INHIBIT DEGRADATION THEREOF WHEN SAID TACTED WITH ACID WHICH CONSISTS IN WETTING SAID MATERIALS WITH AN AQUEOUS SOLUTIN 10.0% BY FROM ABOUT 0.5% BY WEIGHT TO ABOUT 10.0% BY WEIGHT OF AN ALKAL-METAL MOLECULARLY DEHYDRATED GLASSY PHOSPHATE HAVING A MOLAR RATIO OF M2O TO P2O5 OF FROM ABOUT 0.8:1 TO 1.7:1, HERE M IS A MEMBER OF THE GOUP CONSISTING OF AMMONIUM, LITHIUM, SODIUM AND POTASSIUM, REMOVING SAID MATERIALS FROM CONTACT WITH SAID SOLUTION AND DRYING THE SAME, THE PHOSPHATE RETAINED BY SAID MATERIAL INHIBITING DEGRADATION THEREY WHEN WETTED WITH ACID.
US713926A 1946-12-04 1946-12-04 Process of treating cellulosic and similar materials Expired - Lifetime US2580286A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2856330A (en) * 1954-11-08 1958-10-14 Harold N Vagenius Method of treating cotton fabrics

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1501895A (en) * 1919-07-05 1924-07-22 Launcelot W Andrews Composition for fireproofing and other purposes
US1651751A (en) * 1925-03-13 1927-12-06 Morgan & Wright Method of treating fabrics
US1938746A (en) * 1930-01-15 1933-12-12 Ig Farbenindustrie Ag Process for rendering fibrous materials noninflammable
US1978792A (en) * 1924-07-31 1934-10-30 Celanese Corp Aqueous treatment of artificial silk
US2105446A (en) * 1935-04-01 1938-01-11 Monsanto Chemicals Treatment of leather
US2119525A (en) * 1933-12-12 1938-06-07 Wallace T Conn Preservative process for vegetable fibers
US2141189A (en) * 1933-12-22 1938-12-27 Henkel & Cie Gmbh Bleaching and cleansing compositions
US2163085A (en) * 1938-09-15 1939-06-20 Du Pont Flameproofed cellulosic materials
US2201992A (en) * 1939-03-25 1940-05-28 Celanese Corp Treatment of textile yarns and filaments

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1501895A (en) * 1919-07-05 1924-07-22 Launcelot W Andrews Composition for fireproofing and other purposes
US1978792A (en) * 1924-07-31 1934-10-30 Celanese Corp Aqueous treatment of artificial silk
US1651751A (en) * 1925-03-13 1927-12-06 Morgan & Wright Method of treating fabrics
US1938746A (en) * 1930-01-15 1933-12-12 Ig Farbenindustrie Ag Process for rendering fibrous materials noninflammable
US2119525A (en) * 1933-12-12 1938-06-07 Wallace T Conn Preservative process for vegetable fibers
US2141189A (en) * 1933-12-22 1938-12-27 Henkel & Cie Gmbh Bleaching and cleansing compositions
US2105446A (en) * 1935-04-01 1938-01-11 Monsanto Chemicals Treatment of leather
US2163085A (en) * 1938-09-15 1939-06-20 Du Pont Flameproofed cellulosic materials
US2201992A (en) * 1939-03-25 1940-05-28 Celanese Corp Treatment of textile yarns and filaments

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2856330A (en) * 1954-11-08 1958-10-14 Harold N Vagenius Method of treating cotton fabrics

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