US2421218A - Noninflammable waterproofed textiles and method of making same - Google Patents
Noninflammable waterproofed textiles and method of making same Download PDFInfo
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- US2421218A US2421218A US475575A US47557543A US2421218A US 2421218 A US2421218 A US 2421218A US 475575 A US475575 A US 475575A US 47557543 A US47557543 A US 47557543A US 2421218 A US2421218 A US 2421218A
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- textiles
- fabrics
- melamine
- acid
- water
- Prior art date
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- 239000004753 textile Substances 0.000 title description 24
- 238000004519 manufacturing process Methods 0.000 title description 12
- 239000004744 fabric Substances 0.000 description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 239000000463 material Substances 0.000 description 15
- 229920000877 Melamine resin Polymers 0.000 description 14
- 239000000126 substance Substances 0.000 description 13
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 12
- 239000007859 condensation product Substances 0.000 description 11
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 10
- 229940005657 pyrophosphoric acid Drugs 0.000 description 10
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000002023 wood Substances 0.000 description 6
- -1 amide compounds Chemical class 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 150000007974 melamines Chemical class 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
- 229920002955 Art silk Polymers 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- SKHRWYIOPCHLGQ-UHFFFAOYSA-N formaldehyde thiourea 1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC(N)=S.NC1=NC(N)=NC(N)=N1 SKHRWYIOPCHLGQ-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 238000004078 waterproofing Methods 0.000 description 2
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 229940010556 ammonium phosphate Drugs 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- NTBYNMBEYCCFPS-UHFFFAOYSA-N azane boric acid Chemical class N.N.N.OB(O)O NTBYNMBEYCCFPS-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- AUYOHNUMSAGWQZ-UHFFFAOYSA-L dihydroxy(oxo)tin Chemical compound O[Sn](O)=O AUYOHNUMSAGWQZ-UHFFFAOYSA-L 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- GVCGWXSZNUOTDW-UHFFFAOYSA-N sulfo cyanate Chemical compound OS(=O)(=O)OC#N GVCGWXSZNUOTDW-UHFFFAOYSA-N 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229940046549 textile allergenic extract Drugs 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical compound O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
- NFMWFGXCDDYTEG-UHFFFAOYSA-N trimagnesium;diborate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]B([O-])[O-].[O-]B([O-])[O-] NFMWFGXCDDYTEG-UHFFFAOYSA-N 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/92—Fire or heat protection feature
- Y10S428/921—Fire or flameproofing
-
- 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
- Y10T442/2164—Coating or impregnation specified as water repellent
- Y10T442/2197—Nitrogen containing
-
- 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
- the invention relates to the manufacture of waterproof and water-resistant uninfiammable organic fibrous materials, such as textiles, fabrics, artificial silk, and to impregnating substances adapted to be used in connection therewith.
- the textiles and fabrics treated in accordance with this invention and garments made thereof cannot be ignited and do not produce a flame when subjected to combustion. They are also waterproof because the waterproofing substances employed for the impregnation of the textiles and fabrics in accordance with my invention are Application February 11, 1943, Serial No. 475,575
- Garments made'from the materials impregnated according to my invention are, therefore, particularly suited to be worn by military personnel, by firemen and people employed in installations where the danger of fire and explosions prevails.
- Fibres are carbonized instantaneously; no time is available for a slagging action of the artificial resin; the latter, therefore,- cannot be used to render textiles uninflammablej or incombustible. Furthermore, a thorough impregnation with a sufficient quantity of these condensation products leads to very undesired hardening of the textiles and fabrics.
- sulphosphoric acid and oxalic acid may be advantageously used.
- a melamine pyrophosphate was established which consists of two mols melamine and one mol pyrophosphoric acid.
- the textiles and fabrics are preferably first impregnated with the acid and afterwards passed through a melamine bath.
- An insoluble very fine white precipitate is hereby formed which strongly adheres to the fibres and can only be removed by washing or similar water treatment.
- the herewith impregnated textiles and fabrics carbonize quickly when exposed to combustion. but they do not catch fire and do not cause after-glow.
- the pyrophosphates of the cyanuric acid amides and particularly the melamine pyrophosphate show a certain sensitivity to the action of alkalis, salts and certain acids. It forms with salts and alkalis water soluble double salts and with certain acids soluble melamine salts. If the impregnated fabrics are contacted with solutions containing substances of the named tim the 4 tibility of the materials treated in accordance with the invention is accordingly increased.
- condensation products of melamine or of a mixtgrgeof a melamine and thiourea with formalde-
- condensation products and particularly those which contain thiourea added as a hardening and acidifying agent are practically free of salts. acids and alkalis; they become insoluble and not inflammable after being hardened by heating.
- thiourea an acid medium is generated at an elevated temperature due to the formation of a small quantity of sulphocyanic acid; instead of thiourea other suitable acids to harden the melamine formaldehyde condensation product may be used.
- a further advantage of this method resides in a simplification of the process.
- a fabric is impregnated with a 5% solution of pyrophosphoric acid; the excess of the liquid is removed by wringers; the impregnated fabric is passed through a warm chamber; it should not be completely dried to prevent weakening of the fibre.
- the fabric is passed into the melamine methylol solution. A white precipitate is formed in the fibres.
- the fabric is again passed through wringers and then heated to (3., whereby the resin becomes insoluble. The fabric is now ready for use.
- the efiect of this impregnating method is startling. Not only has the fabric become completely uninflammable, but it will retain this property even after a week's exposure or staying in water.
- Colors can also be applied to the treated materials by dyeing; but in this case it is important that the insoluble precipitate is carefully and very uniformly applied to the goods, so as to prevent color spots or stains.
- My method can be applied with equally good results to cotton goods, artificial silk, wool and precipitate is partly dissolved and the combus- 75 similar materials.
- a method of producing non-inflammable waterproof textiles and fabrics comprising treating the said materials with a solution of pyrophosphoric acid and of melamine methylol, im-
- a method of producing non-inflammable waterproof organic textiles and fabrics comprising treating the said materials with a solution of pyrophosphoric acid and of melamine methylol and thiourea, imparting thereby to the fibres a water insoluble precipitate of the melamine and of the pyrophosphoric acid and drying the thus treated materials at a temperature of about 120 to'140 C.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Description
manufacture of uninflammable goods.
. Patented May 27, 1947 E WATERPROOFED TEX- TILES METHOD OF MAKING SAME Frederick F. Pollak, Brooklyn, N. Y.
No Drawing.
6 Claims.
The invention relates to the manufacture of waterproof and water-resistant uninfiammable organic fibrous materials, such as textiles, fabrics, artificial silk, and to impregnating substances adapted to be used in connection therewith. This application is a continuation in part of my pending patent application Ser. No. 460,179, filed September 29, 1942.
The textiles and fabrics treated in accordance with this invention and garments made thereof cannot be ignited and do not produce a flame when subjected to combustion. They are also waterproof because the waterproofing substances employed for the impregnation of the textiles and fabrics in accordance with my invention are Application February 11, 1943, Serial No. 475,575
so strongly incorporated into the fibre and adhere thereto so intensely that they cannot be removed therefrom in spite of energetic'treatment with water.
Garments made'from the materials impregnated according to my invention are, therefore, particularly suited to be worn by military personnel, by firemen and people employed in installations where the danger of fire and explosions prevails.
Many suggestions have been made to impregnate fabrics with fire preventive and with waterproofing substances; however, these methods have not resulted in a successful application in spite of the fact that numerous substances are known which being individually applied to the fibres either prevent its combustionor cannot be removed therefrom by washing. Substances, however, which exert the combinative efiect without umsulfate, ammoniumphosphate, ammonium borates, boric acid, have been recommended for the These substances, however, are watersoluble. Water insoluble organic salts, on the other hand, such as magnesium borate and titanic acid which are recommended for the same purpose may only be incorporated into the fibres by gluing; they are unusable for any practical work.
It has also been suggested to impregnate textiles and fabrics with metastannic acid. The thus treated materials do not burn with a flame; however, they have the great disadvantage of extended or after-glowing. The same phenomenon results from the application of heavy metal salts which due to this grave failure are exempted from practical use; the many inorganic impregnating substances which have been suggested for the manufacture of uninflammable textiles and fabrics or garments made therefrom are not-affected by water and have never met with practical success.
Also certain inorganic components have been recommended for use in the production of uninflammable articles. For instance, a urea formaldehyde condensation product has been suggested to render wood uninflammable.
However, the problem involved in the production of uninflammable wood and uninflammable fabrics is of a widely different nature and therefore cannot be solved on similar lines. Fabrics and textiles have a relatively far greater active surface than wood. The flame expansion, therefore, is much more rapid per surface unit of a fabric, whereas the impregnation capacity is small. Therefore, it is possible to protect wood against inflammation by coating the same with the above mentioned condensation products. If the wood is subjected to combustion the artificial resin has suflicient time to be converted into a voluminous carbonized coating which protects the wood. Fibres, however, are carbonized instantaneously; no time is available for a slagging action of the artificial resin; the latter, therefore,- cannot be used to render textiles uninflammablej or incombustible. Furthermore, a thorough impregnation with a sufficient quantity of these condensation products leads to very undesired hardening of the textiles and fabrics.
Hence, it results that the problem of the manufacture of simultaneously water resistant uninflammable textiles and fabrics has not been solved satisfactorily as yet.
In view of the fact that the prospect of finding an appropriate inorganic impregnating substance was very remote, it is the object of the invention to provide organic impregnating compounds which render fabrics and textiles uninflammable and incombustible and prevent the creation of a long flame.
It is a further object of the invention to provide impregnating compounds of the aforesaid type which being itself practically water-insoluble render the textiles and fabrics to which they are applied inert to the action of water.
It is also an object of the invention to provide compounds of the aforesaid type which stron ly adhere to the fibres and cannot be easily rubbed off.
It is also one of the objects of the invention to provide an impregnating substance which in addition to the above referred to properties prevents the impregnated textiles, and fabrics from becoming hard, brittle, and unelastic.
It is a further object of the invention to provide an impregnating substance for textiles and fabrics which prevents extended glowing.
Furthermore, the compounds which answer the requirements of my inventionmust be colorfree and must not attack the textiles and fabrics to which they are applied.
The last but not the least object of my invention'is that the textiles and fabrics impregnated in accordance with the teachings of my invention in order to be utilized on an expanded commercial scale are resistant to treatments with weak soap and sodiumcarbonate solutions.
Hence, it results that a successful solution of the instant problem presents unexpected-and severe difliculties particularly also in view of the fact that the impregnating substances in order to fully answer the instant requirements must be insoluble in ordinary organic solvents.
In the course of extensive experimentation and research work I have found that'the insoluble compounds of the amidoderivates of the cyanuric acid most suitably comply with all of the aforesaid objects.
However, in order to complete the invention the difficulty of firmly securing these compounds on the textiles and fabrics had to beovercome. In this direction a satisfactorysolution was established by the application of the amido compounds of the cyanuric acid as salts of phosphoric acids and. particularly of the pyrophosphoric acid. This acid has the property of swelling the fibres of the textiles and particularly cotton fabrics to a remarkable degree, whereby. a satisfactory loosening of the fibres is effected and their absorptive capacity for the amide compounds is greatly enhanced.
Instead of pyrophosphoric acid metaphosphoric acid, sulphosphoric acid and oxalic acid may be advantageously used. As a most suitable substance as far as insolubility and securing capacity is concerned, a melamine pyrophosphate was established which consists of two mols melamine and one mol pyrophosphoric acid. The textiles and fabrics are preferably first impregnated with the acid and afterwards passed through a melamine bath. An insoluble very fine white precipitate is hereby formed which strongly adheres to the fibres and can only be removed by washing or similar water treatment. The herewith impregnated textiles and fabrics carbonize quickly when exposed to combustion. but they do not catch fire and do not cause after-glow.
However, and in spite of their resistance to water, the pyrophosphates of the cyanuric acid amides and particularly the melamine pyrophosphate show a certain sensitivity to the action of alkalis, salts and certain acids. It forms with salts and alkalis water soluble double salts and with certain acids soluble melamine salts. If the impregnated fabrics are contacted with solutions containing substances of the named tim the 4 tibility of the materials treated in accordance with the invention is accordingly increased.
In order to avoid this ineiiiciency and to improve the adherence of the precipitate in the treated fibre materials the same are coated with a condensation product of melamine or of a mixtgrgeof a melamine and thiourea with formalde- These condensation products and particularly those which contain thiourea added as a hardening and acidifying agent, are practically free of salts. acids and alkalis; they become insoluble and not inflammable after being hardened by heating. By the addition of thiourea an acid medium is generated at an elevated temperature due to the formation of a small quantity of sulphocyanic acid; instead of thiourea other suitable acids to harden the melamine formaldehyde condensation product may be used.
The use of formaldehyde melamine condensation products to improve the adherence of melamine salts on fibrous materials is a decided advantage as the formation and fixation of the melamine salt and the impregnation of the fibre with the viscous resin solution and the coating may be effected in a single bath. A premature precipitation of the insoluble salts is prevented by the colloidal character of the solution and a complete infiltration of the precipitate into the cell structure of the textiles and fabrics is assured;
A further advantage of this method resides in a simplification of the process. When using other coating methods it is generally necessary toapply three consecutive treatment stages, whereas one or-two coating steps will be 'sufiicient in the instant case.
The following example may serve to illustrate the invention:
15 parts of 40% formaldehyde solution, slightly alkalized bysodiumhydrate (pH 8), 12.6 parts of melamine, and 40 parts of water are heated and kept boiling for 20-30 minutes until the formation of the methylol is completed; no precipitate must be formed in the solution when diluted with an excess of water. After cooling one part of thiourea in 20 parts of water is added.
- A fabric is impregnated with a 5% solution of pyrophosphoric acid; the excess of the liquid is removed by wringers; the impregnated fabric is passed through a warm chamber; it should not be completely dried to prevent weakening of the fibre. Hereafter, the fabric is passed into the melamine methylol solution. A white precipitate is formed in the fibres. The fabric is again passed through wringers and then heated to (3., whereby the resin becomes insoluble. The fabric is now ready for use.
The efiect of this impregnating method is startling. Not only has the fabric become completely uninflammable, but it will retain this property even after a week's exposure or staying in water.
when colored fabrics are used, they will not appreciably change in color; a somewhat cloudy shade may be imparted to them sometimes; this, however, may be easily remedied by the use of a suitably colored solution of the resin.
Colors can also be applied to the treated materials by dyeing; but in this case it is important that the insoluble precipitate is carefully and very uniformly applied to the goods, so as to prevent color spots or stains.
My method can be applied with equally good results to cotton goods, artificial silk, wool and precipitate is partly dissolved and the combus- 75 similar materials.
tions in percentages of the material used, in the time and temperature of the different heating steps in the sequence thereof, in the mode of application and in the use of the products of reaction can be made by one skilled in the art to suit different requirements.
I claim:
1. As a new product of manufacture a noninflammable waterproof organic fibre material impregnated with a water insoluble melamine salt of pyrophosphoric acid and coated with a melamine formaldehyde condensation product.
2. As a new product of manufacture. a noninflammable waterproof organic fibre material impregnated with a water insoluble melamine of pyrophosphoric acid and coated with a mixed melamine thiourea formaldehyde condensation product.
3. As a new product of manufacture a noninflammable waterproof organic fibre material impregnated with a water insoluble melamine methylol pyrophosphate and coated with a melamine formaldehyde condensation product.
4. As a new product of manufacture a noninflammable waterproof organic fibre material impregnated with water insoluble melamine methylol pyrophosphate and coated with a mixed melamine thiourea formaldehyde condensation product.
5. A method of producing non-inflammable waterproof textiles and fabrics comprising treating the said materials with a solution of pyrophosphoric acid and of melamine methylol, im-
parting thereby to the fibres a water insoluble precipitate of the melamine and of the pyrophosphoric acid, and drying the thus treated materials at a temperature of about to C.
6. A method of producing non-inflammable waterproof organic textiles and fabrics comprising treating the said materials with a solution of pyrophosphoric acid and of melamine methylol and thiourea, imparting thereby to the fibres a water insoluble precipitate of the melamine and of the pyrophosphoric acid and drying the thus treated materials at a temperature of about 120 to'140 C.
FREDERICK F. POLLAK,
REFERENCES CITED The following references are of record in the file of this patent:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US475575A US2421218A (en) | 1943-02-11 | 1943-02-11 | Noninflammable waterproofed textiles and method of making same |
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US475575A US2421218A (en) | 1943-02-11 | 1943-02-11 | Noninflammable waterproofed textiles and method of making same |
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US2421218A true US2421218A (en) | 1947-05-27 |
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US475575A Expired - Lifetime US2421218A (en) | 1943-02-11 | 1943-02-11 | Noninflammable waterproofed textiles and method of making same |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2470042A (en) * | 1945-11-26 | 1949-05-10 | Ici Ltd | Process for flameproofing combustible celluloseic material and product resulting therefrom |
US2660542A (en) * | 1948-11-26 | 1953-11-24 | Glenn L Martin Co | Flameproofed article and method of making same |
US2665733A (en) * | 1949-09-20 | 1954-01-12 | Us Rubber Co | Cellulose fiber tire casing protected against heat aging |
US2779691A (en) * | 1950-04-11 | 1957-01-29 | American Cyanamid Co | Method of imparting flame-resistance to cellulosic materials |
DE977415C (en) * | 1951-08-03 | 1966-05-18 | Ciba Geigy | Process for making textiles flame resistant |
US3625753A (en) * | 1969-10-14 | 1971-12-07 | American Cyanamid Co | Flame retardant for textiles |
US3655422A (en) * | 1970-09-18 | 1972-04-11 | Kimberly Clark Co | Fire retarding treatment |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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US1501895A (en) * | 1919-07-05 | 1924-07-22 | Launcelot W Andrews | Composition for fireproofing and other purposes |
US2071353A (en) * | 1935-07-13 | 1937-02-23 | Sylvania Ind Corp | Compositions for fireproofing |
GB476043A (en) * | 1935-05-01 | 1937-11-29 | Baverische Stickstoffwerke Akt | An improved method of fireproofing solid combustible substances |
US2197357A (en) * | 1935-09-28 | 1940-04-16 | Ciba Products Corp | Condensation products of amino-triazine, aldehyde, and alcoholic group-containing compounds and processes of making same |
US2307876A (en) * | 1939-01-13 | 1943-01-12 | Tootal Broadhurst Lee Co Ltd | Production of glazed fabrics |
-
1943
- 1943-02-11 US US475575A patent/US2421218A/en not_active Expired - Lifetime
Patent Citations (5)
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 |
GB476043A (en) * | 1935-05-01 | 1937-11-29 | Baverische Stickstoffwerke Akt | An improved method of fireproofing solid combustible substances |
US2071353A (en) * | 1935-07-13 | 1937-02-23 | Sylvania Ind Corp | Compositions for fireproofing |
US2197357A (en) * | 1935-09-28 | 1940-04-16 | Ciba Products Corp | Condensation products of amino-triazine, aldehyde, and alcoholic group-containing compounds and processes of making same |
US2307876A (en) * | 1939-01-13 | 1943-01-12 | Tootal Broadhurst Lee Co Ltd | Production of glazed fabrics |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2470042A (en) * | 1945-11-26 | 1949-05-10 | Ici Ltd | Process for flameproofing combustible celluloseic material and product resulting therefrom |
US2660542A (en) * | 1948-11-26 | 1953-11-24 | Glenn L Martin Co | Flameproofed article and method of making same |
US2665733A (en) * | 1949-09-20 | 1954-01-12 | Us Rubber Co | Cellulose fiber tire casing protected against heat aging |
US2779691A (en) * | 1950-04-11 | 1957-01-29 | American Cyanamid Co | Method of imparting flame-resistance to cellulosic materials |
DE977415C (en) * | 1951-08-03 | 1966-05-18 | Ciba Geigy | Process for making textiles flame resistant |
US3625753A (en) * | 1969-10-14 | 1971-12-07 | American Cyanamid Co | Flame retardant for textiles |
US3655422A (en) * | 1970-09-18 | 1972-04-11 | Kimberly Clark Co | Fire retarding treatment |
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