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US2949385A - Fire-retardant process - Google Patents

Fire-retardant process Download PDF

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Publication number
US2949385A
US2949385A US333601A US33360153A US2949385A US 2949385 A US2949385 A US 2949385A US 333601 A US333601 A US 333601A US 33360153 A US33360153 A US 33360153A US 2949385 A US2949385 A US 2949385A
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United States
Prior art keywords
water
fire
product
cellulosic
hydrolyzed
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US333601A
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John E Malowan
Morris L Nielsen
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Monsanto Chemicals Ltd
Monsanto Chemical Co
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Monsanto Chemicals Ltd
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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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/667Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing phosphorus in the main chain

Definitions

  • fire-resistance and flame-resistance result from the treatment of a base material such as cloth with various chemicals so that it becomes resistant to the propagation of flame across its surface after the igniting flame has been removed; that is, a flameresistant material will not support combustion independently of an external source of heat. In contact with an open flame, however, or at elevated, temperatures, flame-resistant cellulosic material can be expected to char and decompose.
  • the products of the present invention exhibit the properties of fire-resistance orfire-retardancy, while at the same time maintaining to a large degree the original hand of the material.
  • the colonphysical appearance andthe property ofsoftness are not substantially'atfected by the present treatment,
  • the nitrogenand phosphorus-containing products utilized in the present invention are produced by the hydrolysis of the substantially water-insoluble reaction product of phosphorus oxychloride and ammonia, which is 2,949,385 Patented Aug. 16, 1960 obtained from a reaction carried out at a temperature in the range of from 155 C. to 200 C.
  • the said bydrolysis is conducted by treatment of the aforementioned condensation product with from 10% to 35% by weight of water at a temperature in the range of from C. to 150 C. at a pressure of about 2 atmospheres or more.
  • the hydrolysis may also ibe conducted in the presence of minor proportions of dilute mineral acids or bases as catalysts.
  • the above reaction results in the production of a water-soluble product forming viscous solutions with water.
  • the molecular weight of the water-soluble hydrolysis product is preferably in the range of from 200- 250. Solutions containing up to 50% by weight of solids may readily be prepared.
  • the nitrogen-phosphorus atomic ratio of the hydrolyzed product lies in the range of 1.25:1 to 1.9:1, which represents a product desirable from the standpoint of providing a material which may combine with an organic resin in a fire-retardant composition to release nitrogen compounds as gases upon exposure to fire. C0nsequently, when a resin is present, the entire coating composition swells to provide a porous insulating layer when subjected to extreme heat, thereby protecting the treated fabric or other combustible cellulosic material, such as cotton, straw, paper, bagasse, rayon and the like.
  • Cellulosic textile products are impregnated or coated with the above-described water-soluble hydrolyzed prod-- not by immersing the said textile materials in previously prepared, aqueous solutions of the hydrolyzed product.
  • Aqueous solutions are preferred but other solvents may also be used.
  • the concentration of the solutions may vary over a wide range depending upon the desired addon which is to be obtained. In general, solutions containing from 5% to 50% by weight of the hydrolyzed product may be employed to obtain an add-on in the range of from 5% to 5 0% by weight relative to the weight of the base material. Fabrics which are to withstand washing are preferably treated to obtain an add-on of. 20% to 25% by weight.
  • a fire-retardant composition in which, the essential constituent is the above described hydrolyzed phosphorus-nitrogemcomtainingcomponent.
  • This material may alsobe formulatedincombination with various organic resinous materials, such: as the aminoplast resins and. intermediate conden-" sationproducts thereof.
  • a resinous-.component when employed it maybe-applied in the range of-0.5,% to2-5, by weight, calculated as final add-on of the final material.
  • the present invention contemplates combination compositions employing amine-aldehyde, aminoaldehyde, iminealdehyde and iminoaldehyde condensation products.
  • a typical example of resins of this class is a urea-formaldehyde resin.
  • Aminoplast resins are discussed in Modern Plastics, 17, 433 (1939). Other aminoplasts are described in C. Ell-is, Chemistry of Synthetic Resins, chapter 25 (Reinhold Publishing Company, 1939), and R. Nauth, Chemistry and Technology of Plastics, chapter 3 (Reinhold Publishing Company, 1947). Further examples are the formaldehyde condensation products with urea, melamine, thiourea-guanidine, cyanamide, dicyandiamide, aniline, para-toluene, sulfonamide and also the corresponding acetaldehyde and furfural condensation prodnets in this same relationship.
  • Such resinous compositions may employ high or low degrees of methylolation (or the corresponding acetyl or furfural substitution) such as from 1 to 6 methylol radicals per mole of the acceptor compound in the case of melamine.
  • methylolation or the corresponding acetyl or furfural substitution
  • alkylated modifications .of such resins is likewise contemplated, particularly in the butylated modifications, such as are conventional in urea-formaldehyde and melamine-formaldehyde resins. Mixtures of such resins or the addition of other types of resins may also be employed.
  • the dry components such as a waterinsoluble resin may be suspended in water with the aid of dispersing agents and the suspension including the water-soluble hydrolyzed product may thusbe applied to fibrous materials in known manner.
  • the hydrolyzed product in combination with the organic resinous con 'stituent apparently adheres to, is impregnated upon, or is adsorbed by cellulosic base materials which are to be treated, thereby reducing the burning tendency of the otherwise combustible cellulosic material.
  • Example 1 A 40% solution of the hydrolyzed water-soluble derivat-ive of the water-insoluble product of phosphorous oxychloride and anhydrous ammonia was applied to cotton cloth to give a 100% increase in weight in the wet state. cured at 150 C. for 10 minutes. After washing the treated cloth showed a high degree of flame-resistance.
  • Example 2 after 36 washings per-formed at a temperature of 120 F.
  • the details of the testing procedure utilized in testing the flameproofing qualities of the present compositions are shown in the book by R. W. Little entitled Flameproofing Fabric Materials (Reinhold Publishing Company, 1947).
  • Example 3 Pieces of filter paper were impregnated with a solution containing 2.5 g. of the water-soluble hydrolyzed derivat-ive of the water-insoluble reaction product of phosphorus. oxychloride and anhydrous ammonia, said solution also containing 10 g. of methylolated melamine and 50 g. of water. After drying and curing at 150 C. for 10 minutes, the samples were tested and found to be flameproofed. On exposure to a high humidity (90%) at 50 C. in a closed cabinet for 24 hours, there was practically no increase of Weight, indicating that the treated material was not hygroscopic. It was also found that soaking a piece of the treated paper in Water for 30 minutes did not reduce the fire-retardant qualities.
  • a process for the treatment of cellulosic textile products which comprises applying to a cellulosic textile prodnot a previously-prepared water-soluble hydrolysis prodnet of the water-insoluble reaction product of phosphorus The cloth was then dried at 105 C. and then oxychloride and anhydrous ammonia having been formed at a temperature in the range of from 155 C.
  • said water-soluble hydrolysis product exhibiting a pH within the range of from 7.0 to 7.5 in aqueous solu tion and having a molecular weight in the range of from 200-250, and thereafter heating said treated cellulosic product to at least C., but below 200 C., said treated cellulosic product containing from 5% to 50% by weight of the said hydrolysis product wherein the said hydrolysis product is combined with the said cellulosic textile product.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Description

FlRE-RETARDANT PROCESS John E. Malowan, Dayton, and Morris L. Nielsen, Centerville, Ohio, assignors to Monsanto Chemical Company, St. Louis, Mo., a corporation of Delaware No Drawing. Filed Jan. 27, 1953, Ser. No. 333,601 1 Claim. (Cl. 117-138) This invention relates to the treatment of cellulosic materials in order to improve their resistance to fire.
It is an object of the invention to provide a method for rendering cellulosic materials fire-resistant. It is another object of the invention to provide flame-resistant cellulosic products. Still another object of the invention is the modification of textile fibers and other combustible materials containing cellulose to render the same resistant to fire.
It is known in the prior art that cellulosic materials such as textile products can be modified to improve their resistance to fire by treatment with phosphorus compounds. For example, U.S. Patent 2,401,440 describes the treatment of cellulosic products such as alkalized cellulose by treatment first with phosphorus oxychloride and then with ammonia. While the products produced by the process described in this patent contain chemically bound phosphonamide groups, the treatment involved the use of chemical reagents which the textile processing industry was not generally equipped to handle. For this reason a simpler method which could be used in the ordinary textile plant without special equipment or skills was greatly to be desired.
In accordance with the terminology which has been developed in this field fire-resistance and flame-resistance result from the treatment of a base material such as cloth with various chemicals so that it becomes resistant to the propagation of flame across its surface after the igniting flame has been removed; that is, a flameresistant material will not support combustion independently of an external source of heat. In contact with an open flame, however, or at elevated, temperatures, flame-resistant cellulosic material can be expected to char and decompose.
The products of the present invention exhibit the properties of fire-resistance orfire-retardancy, while at the same time maintaining to a large degree the original hand of the material. The colonphysical appearance andthe property ofsoftness are not substantially'atfected by the present treatment,
It has been found that an improved-fireeretardantitreatment of combustible cellulosic materials such as cotton and other cellulosic derivatives including cellulose acetate, cellulose nitrate, and regenerated cellulose may be provided with the hydrolyzed water-soluble, nitrogenand phosphorus-containing product described in copending application Serial No. 333,602, filed January 27, 1953, now Patent No. 2,749,233, which application is assigned to the same assignee as is the present case. This treatment results in the production of a permanent flameresistant material of excellent hand, which exhibits substantially the physical appearance and property of softness of the untreated fabric.
According to the copending application referred to above, the nitrogenand phosphorus-containing products utilized in the present invention are produced by the hydrolysis of the substantially water-insoluble reaction product of phosphorus oxychloride and ammonia, which is 2,949,385 Patented Aug. 16, 1960 obtained from a reaction carried out at a temperature in the range of from 155 C. to 200 C. The said bydrolysis is conducted by treatment of the aforementioned condensation product with from 10% to 35% by weight of water at a temperature in the range of from C. to 150 C. at a pressure of about 2 atmospheres or more. The hydrolysis may also ibe conducted in the presence of minor proportions of dilute mineral acids or bases as catalysts. The above reaction results in the production of a water-soluble product forming viscous solutions with water. The molecular weight of the water-soluble hydrolysis product is preferably in the range of from 200- 250. Solutions containing up to 50% by weight of solids may readily be prepared.
The nitrogen-phosphorus atomic ratio of the hydrolyzed product lies in the range of 1.25:1 to 1.9:1, which represents a product desirable from the standpoint of providing a material which may combine with an organic resin in a fire-retardant composition to release nitrogen compounds as gases upon exposure to fire. C0nsequently, when a resin is present, the entire coating composition swells to provide a porous insulating layer when subjected to extreme heat, thereby protecting the treated fabric or other combustible cellulosic material, such as cotton, straw, paper, bagasse, rayon and the like.
Cellulosic textile products are impregnated or coated with the above-described water-soluble hydrolyzed prod-- not by immersing the said textile materials in previously prepared, aqueous solutions of the hydrolyzed product. Aqueous solutions are preferred but other solvents may also be used. The concentration of the solutions may vary over a wide range depending upon the desired addon which is to be obtained. In general, solutions containing from 5% to 50% by weight of the hydrolyzed product may be employed to obtain an add-on in the range of from 5% to 5 0% by weight relative to the weight of the base material. Fabrics which are to withstand washing are preferably treated to obtain an add-on of. 20% to 25% by weight. In the treatment of rayon it has also been found that dimensional stabilization is greatly improved as a result of the deposition of the said watersoluble hydrolyzed material. After impregnation of the textile fabric and in order to produce a wash-fast, fireretardant fabric the impregnated fabric is dried and then subjected to a temperature of at least but below 200- C. However, if it is not necessary to-produce a wash-fast product the "heating step may beomitted.
In accordance with this invention, a fire-retardant composition is provided in which, the essential constituent is the above described hydrolyzed phosphorus-nitrogemcomtainingcomponent. This material may alsobe formulatedincombination with various organic resinous materials, such: as the aminoplast resins and. intermediate conden-" sationproducts thereof. When a resinous-.componentisemployed it maybe-applied in the range of-0.5,% to2-5, by weight, calculated as final add-on of the final material. The present invention contemplates combination compositions employing amine-aldehyde, aminoaldehyde, iminealdehyde and iminoaldehyde condensation products. A typical example of resins of this class is a urea-formaldehyde resin. Aminoplast resins are discussed in Modern Plastics, 17, 433 (1939). Other aminoplasts are described in C. Ell-is, Chemistry of Synthetic Resins, chapter 25 (Reinhold Publishing Company, 1939), and R. Nauth, Chemistry and Technology of Plastics, chapter 3 (Reinhold Publishing Company, 1947). Further examples are the formaldehyde condensation products with urea, melamine, thiourea-guanidine, cyanamide, dicyandiamide, aniline, para-toluene, sulfonamide and also the corresponding acetaldehyde and furfural condensation prodnets in this same relationship. Such resinous compositions may employ high or low degrees of methylolation (or the corresponding acetyl or furfural substitution) such as from 1 to 6 methylol radicals per mole of the acceptor compound in the case of melamine. The use of alkylated modifications .of such resins is likewise contemplated, particularly in the butylated modifications, such as are conventional in urea-formaldehyde and melamine-formaldehyde resins. Mixtures of such resins or the addition of other types of resins may also be employed.
In addition to the synthetic type of resins as set forth above, it is also possible to utilize nitrogen-containing resinous materials derived from natural sources such as casein. The casein compositions, insolubilized by formaldeh'yde, are of particular utility for this purpose. Polyamide resins which may be brought into solution or dispersion' may also be introduced into the compositions of the present invention.
In the application of the above combination composi tions including essential water-soluble hydrolyzed product described'above, the dry components such as a waterinsoluble resin may be suspended in water with the aid of dispersing agents and the suspension including the water-soluble hydrolyzed product may thusbe applied to fibrous materials in known manner. The hydrolyzed product in combination with the organic resinous con 'stituent apparently adheres to, is impregnated upon, or is adsorbed by cellulosic base materials which are to be treated, thereby reducing the burning tendency of the otherwise combustible cellulosic material.
In combinations utilizing an organic resinous material dissolved or dispersed in water, together with the hydrolyzed compositions described above, it has been found that the latter constituent should be present in the range of from 0.5% to 25% by weight based upon the dry materials, a preferred range or composition for fabrics subject to washing being from to by weight.
The following examples illustrate the invention.
Example 1 A 40% solution of the hydrolyzed water-soluble derivat-ive of the water-insoluble product of phosphorous oxychloride and anhydrous ammonia was applied to cotton cloth to give a 100% increase in weight in the wet state. cured at 150 C. for 10 minutes. After washing the treated cloth showed a high degree of flame-resistance.
Example 2 after 36 washings per-formed at a temperature of 120 F. The details of the testing procedure utilized in testing the flameproofing qualities of the present compositions are shown in the book by R. W. Little entitled Flameproofing Fabric Materials (Reinhold Publishing Company, 1947).
Example 3 Pieces of filter paper were impregnated with a solution containing 2.5 g. of the water-soluble hydrolyzed derivat-ive of the water-insoluble reaction product of phosphorus. oxychloride and anhydrous ammonia, said solution also containing 10 g. of methylolated melamine and 50 g. of water. After drying and curing at 150 C. for 10 minutes, the samples were tested and found to be flameproofed. On exposure to a high humidity (90%) at 50 C. in a closed cabinet for 24 hours, there was practically no increase of Weight, indicating that the treated material was not hygroscopic. It was also found that soaking a piece of the treated paper in Water for 30 minutes did not reduce the fire-retardant qualities. V In the application of the water-soluble hydrolyzed derivative of the water-insoluble reaction product of phosphorus oxychloride and anhydrous ammonia as coat ing compositions on combustible materials to render them fire-resistant, it is also contemplated that other chemical components may be used in combination therewith. For example, other fire-retardant chemicals such as antimony oxide may also be applied either as a separate operation of simultaneously with the present materials. In such a combined-treatment the present hydrolyzed material is of particular utility in repressing the catalytic tendency of the metal oxides to exhibit the characteristic afterglow.
What is claimed is:
A process for the treatment of cellulosic textile products which comprises applying to a cellulosic textile prodnot a previously-prepared water-soluble hydrolysis prodnet of the water-insoluble reaction product of phosphorus The cloth was then dried at 105 C. and then oxychloride and anhydrous ammonia having been formed at a temperature in the range of from 155 C. to 250 C., said water-soluble hydrolysis product exhibiting a pH within the range of from 7.0 to 7.5 in aqueous solu tion and having a molecular weight in the range of from 200-250, and thereafter heating said treated cellulosic product to at least C., but below 200 C., said treated cellulosic product containing from 5% to 50% by weight of the said hydrolysis product wherein the said hydrolysis product is combined with the said cellulosic textile product.
References Cited in the file of this patent UNITED STATES PATENTS UNITEb STATES VOFFICE CERTIFICATE OF CORRECTION Patent N00 2,949 385 August 16 1960 John E. Melowan et :11;
I It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 4 line 29 for "of" read or Signed and sealed this 18th day o fi'June 1963o (SEAL) Attest:
RNEST w. SWIDER DAVID LADD Attesting Officer Commissioner of Patents
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3248257A (en) * 1960-10-24 1966-04-26 Woods Conversion Company Flame-resistant mineral fiber tile

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2163085A (en) * 1938-09-15 1939-06-20 Du Pont Flameproofed cellulosic materials
US2424831A (en) * 1942-11-24 1947-07-29 Quaker Chemical Products Corp Composition for waterproofing and fireproofing textile material, and the treated material
US2582181A (en) * 1949-03-25 1952-01-08 Rudolf F Hlavaty Fireproofing compositions containing water-insoluble phosphorylamides, and articles fireproofed therewith
US2596496A (en) * 1948-12-30 1952-05-13 Monsanto Chemicals Noncombustible coating composition and method of applying
US2596935A (en) * 1948-12-30 1952-05-13 Monsanto Chemicals Nitrogen-phosphorus composition and process for same

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2163085A (en) * 1938-09-15 1939-06-20 Du Pont Flameproofed cellulosic materials
US2424831A (en) * 1942-11-24 1947-07-29 Quaker Chemical Products Corp Composition for waterproofing and fireproofing textile material, and the treated material
US2596496A (en) * 1948-12-30 1952-05-13 Monsanto Chemicals Noncombustible coating composition and method of applying
US2596935A (en) * 1948-12-30 1952-05-13 Monsanto Chemicals Nitrogen-phosphorus composition and process for same
US2582181A (en) * 1949-03-25 1952-01-08 Rudolf F Hlavaty Fireproofing compositions containing water-insoluble phosphorylamides, and articles fireproofed therewith

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3248257A (en) * 1960-10-24 1966-04-26 Woods Conversion Company Flame-resistant mineral fiber tile

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