US2582181A - Fireproofing compositions containing water-insoluble phosphorylamides, and articles fireproofed therewith - Google Patents
Fireproofing compositions containing water-insoluble phosphorylamides, and articles fireproofed therewith Download PDFInfo
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- US2582181A US2582181A US83514A US8351449A US2582181A US 2582181 A US2582181 A US 2582181A US 83514 A US83514 A US 83514A US 8351449 A US8351449 A US 8351449A US 2582181 A US2582181 A US 2582181A
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- phosphorylamides
- fireproofing
- fireproofed
- insoluble
- articles
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Links
- 238000004079 fireproofing Methods 0.000 title claims description 24
- 239000000203 mixture Substances 0.000 title description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 24
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 239000007795 chemical reaction product Substances 0.000 claims description 14
- 239000003973 paint Substances 0.000 claims description 9
- 239000004615 ingredient Substances 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 description 43
- 239000011230 binding agent Substances 0.000 description 14
- 239000000835 fiber Substances 0.000 description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 229910021529 ammonia Inorganic materials 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000002657 fibrous material Substances 0.000 description 5
- 229910044991 metal oxide Inorganic materials 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 150000002894 organic compounds Chemical class 0.000 description 4
- 229920002689 polyvinyl acetate Polymers 0.000 description 4
- 239000011118 polyvinyl acetate Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000010791 quenching Methods 0.000 description 4
- 230000000171 quenching effect Effects 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 229910000410 antimony oxide Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- DMSZORWOGDLWGN-UHFFFAOYSA-N ctk1a3526 Chemical compound NP(N)(N)=O DMSZORWOGDLWGN-UHFFFAOYSA-N 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 229920001756 Polyvinyl chloride acetate Polymers 0.000 description 2
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 239000007764 o/w emulsion Substances 0.000 description 2
- 150000003012 phosphoric acid amides Chemical class 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- -1 titanium dioxide Chemical class 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- GGMPTLAAIUQMIE-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobiphenyl Chemical group ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=CC=CC=C1 GGMPTLAAIUQMIE-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical class C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- IKWTVSLWAPBBKU-UHFFFAOYSA-N a1010_sial Chemical compound O=[As]O[As]=O IKWTVSLWAPBBKU-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000413 arsenic oxide Inorganic materials 0.000 description 1
- 229960002594 arsenic trioxide Drugs 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- ZTQSADJAYQOCDD-UHFFFAOYSA-N ginsenoside-Rd2 Natural products C1CC(C2(CCC3C(C)(C)C(OC4C(C(O)C(O)C(CO)O4)O)CCC3(C)C2CC2O)C)(C)C2C1C(C)(CCC=C(C)C)OC(C(C(O)C1O)O)OC1COC1OCC(O)C(O)C1O ZTQSADJAYQOCDD-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/18—Fireproof paints including high temperature resistant paints
-
- 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
- Y10T442/2631—Coating or impregnation provides heat or fire protection
- Y10T442/2672—Phosphorus containing
- Y10T442/2689—A phosphorus containing compound and a nitrogen containing compound
Definitions
- This invention relates to a material for and a method of fireproofing.
- the material may be used for fireproofing many materials, natural or synthetics and their combinations. It may be used, for example nziiseetmfieesibregemeiez rial of any nature, whether the fibrous material is merely in fibrous form or woven or felted or 7 be flreproofed.
- Another object of the invention is to provide a fireproofing material which is permanent in character and which cannot be removed by washing, weathering, or by the solvents used in-dry cleaning or by reaction of weather conditions, as it is permanent.
- Another object is to provide a fireproofing material of such efficiency that relatively, small amounts of it will prove adequate for fireproofing and thus accomplish a saving in total weight of fireproofed material.
- a further object is to provide a fireproofing agent which is non-corrosive and non-toxic, so that the agent itself and the material which has been treated with it can be freely and safely handled.
- fireproofing materials are now known and most of such materials have generally one or more of the following defects: They are ineificient and substantial weights are required. They are corrosive and toxic. They are not permanent in character.
- Another class of fireprooflng materials includes chlorinated waxes and resins which may be used along with or in combination with various metallic oxides for fireproofing. In the case of these materials also large quantities are required for efiectiveness and they have the further disadvantage that they are corrosive in character and form hydrochloric acid, particularly at elevated temperatures.
- the firperoofing material of the present inven-' tion comprises the amides, imidesg d ii nidoamides of phosphoric ari'd thi'ophbs'phoric acids, as Well as the nitride of phosphoric acid. Tests have shown that these materials are excellent fire and flameproofing agents and that they are effective in very much smalleramounts than the metallic oxides used at present, such as the oxides of tin, aluminum and antimony. They have the further advantage that they are non-poisonous and non-corrosive and that they are insoluble in water and in most available solvents.
- Phosphoric acid may be given the following structural formula:
- This material is phosphorylnitride and comprises a white inert powder which forms a black glass at red heat.
- fireproofing material of this invention is the water insoluble, chlorine free,
- reaction product of phosphorus oxychloride with anhydrous ammonia This reaction product consists of a mixture of phosphoryltriamide, phosphorylimidoamide and polyphosphorylamides. It ispossible, though very difficult, to separate the three components of the reaction product, but for the purpose of this invention it is not necessary since all three are powerful fireproofing agents. On the other hand, it is readily possible to control the proportion in which they are formed by controlling the conditions of the reaction; for example, when the reaction is affected at low temperatures, the phosphoryltriamide predominates in the reaction product, while higher temperatures favor the formation of the prosphorylimidoamide and polyphosphorylamides.
- phosphorylamides will be used throughout the specification and claims to indicate the mixture of phosphoric acid amides which is the reaction product of phosphorus oxychloride and anhydrous ammonia, as described above.
- fireproofing may be accomplished as a result of two actions: (1) the formation, upon heating, of a fire quenching gas such as ammonia, carbon dioxide or chlorine, which gas smothers the flame; and (2) the formation, upon heating, of a melted material which covers the combustible fibers or article and prevents burning.
- a fire quenching gas such as ammonia, carbon dioxide or chlorine
- the metallic oxides and some salts such as borax operate in the latter manner to produce, upon melting, a glass-like material.
- the ammonia and chlorine compounds act in the former manner to produce fire quenching gases.
- the amides and imides of phosphoric and thiophosphoric acid are extremely effective because they partake of both methods of quenching fire. Upon heating a fire quenching gas is formed and also a glass-like material is produced as a result of melting, and this material covers the fibers or 7 f with Wbib. 1? i 2 ieqa qp e ts l 4 burning. The phosphorylnitride acts in the same way.
- the chlorinated paraflin acts as a binder and since it is thermally unstable and upon decomposition hydrochloric acid is vformed, it further enhances the fireproofing quality of the mixture.
- Emulsifier 2 This is another example of an oil-in-water emulsion using chlorinated napthalene as the thermally'unstable binder. The solvent used makes this emulsion safe to handle. In the same manner, other thermally unstable chlorinated organic compounds suitable as binders for the phosphorylamides can also be used. These could be neoprene, pentachlorobiphenyl, chlorinated, natural 70 or synthetic rubber, and chloropolystyrene.
- Powdered phosphorylamides 75 Powdered polyvinylchloride acetate copolymer 25 This is another example of dry binding by means of heat.
- the phosphorylamides because of their nature, are preferably used with a binder. As indicated by the examples enumeratedabove,”thermally unstable chlorinated organic compounds v.are preferred because they are noncombustible. This should not be presumed to exclude other binders.
- Parts Phosphorylamides -I 50 Commercial polyvinyl acetate emulsion 45 Tricresylphosphate The polyvinyl acetate film alone supports fire but in the presence of the phosphorylamides it does not burn. On the other hand, the total effectiveness as a fireproofing mixture is much les than that of any of Examples I--VII, and the use of binders which support fire is recommended only when other considerations prevent the use of the thermally unstable chlorinated binders.
- Other film forming, water insoluble materials may also be used. Among these are polystyrene emulsion, synthetic and natural latexes, and alkyd resin emulsions.
- Example VIII is a fireproof enamel;
- Example IX a fireproof paint;
- Example X a fireproof lacquer.
- a flameproof surface coating may be made in which the phosphorylamides constitute from 15% to 50% of the paint.
- the pigments used in these fireproof surface coatings are those normally used in the paint industry. Their choice depends upon the purpose they are to serve in the surface coating, andthey are generally chosen from the group of inorganic metallic oxides, carbonates, sulphides and sulphates such as titanium dioxide, lithopone, lead oxides and zinc oxides.
- the materials treated by the products above mentioned have beenreferred to as being fireproofed.
- the result of the treatment is to make these materials greprg of and gam eproof. and also glowprop f, That is to say, the material treated,
- the amount of phosphorylamides necessary satisfactorily to fireproof such materials may be as little as 10% by weight of the material, irrespective of any contribution of the binder to the total fireproofing effect. It is to be remembered that the binders proposed herein are in some cases not fireproof or fire resistant in themselves. However, as much as of phosphorylamides may be added without detrimental effect on the treated materials. In usual practice the total of the solids add on of 20% to 30% is satisfactory.
- the phosphorylamides may be mixed with or applied to a material to be fireproofed in almost any manner, either as the material is made or processed or after it has been made.
- a fireproofing paint comprising 20-50% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia and 80-50% of normal paint ingredients includll ,QPE PEEUE Q.EXQFQ? E 5 winder-I.-.
- a fireproofing paint comprising 20-50% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia and 80-50% of normal paint ingredients, including pigment, resin and solvent; a
- a fireproofing composition comprising 20- 50% of the water insoluble reaction product of phosphorous oxychlorlde with anhydrous ammonia suspended in 80-50% of a solution of thermally unstable chlorinated organic compounds as a binder.
- a fireproofing composition comprising 50- 90% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia intimately mixed with 50-10% of thermally unstable chlorinated organic compounds as a binder.
- a fireproofiing composition comprising 20- 50% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia suspende in'80-50% of a material selected from the group consisting of polyvinyl acetate emulsion, polystyrene emulsion, synthetic and natural rubber latexes and alkyd resin emulsion as binders.
- An article of manufacture comprising a mass of fibrous material fireproofed by the addition of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia in the proportion of 10-80% of the weight of the article.
- An article of manufacture comprising a mass of fibrous material fireproofed by the composition of claim 5.
- a glowproofingcomposition comprising polyvinyl chloride and the water insoluble reaction product of phosphoryl chloride with anhydrous ammonia.
- a glowproofing composition comprising polyvinyl acetate and the water insoluble reaction product of phosphoryl chloride with anhydrous ammonia.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Fireproofing Substances (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Jr.) mn Ll'ihidifil.
smears; Patented Jam 8 1952 2 2 1 1 UN OFFICE FIREPROOFING COMPOSITIONS CONTAIN- ING 'WATER-INSOLUBLE PHOSPHORYL- AMIDES, AND ARTICLES FIREPROOFED THEREWITH John Tru'hl'ar, Clarendon Hills, and Athan A. Pantsios, Chicago, 111., assignors to Rudolf F. Hlavaty, Westchestcr, Ill.
No Drawing. Application March 25, 1949, Serial No. 83,514
This invention relates to a material for and a method of fireproofing. The material may be used for fireproofing many materials, natural or synthetics and their combinations. It may be used, for example nziiseetmfieesibregemeiez rial of any nature, whether the fibrous material is merely in fibrous form or woven or felted or 7 be flreproofed.
Another object of the invention is to provide a fireproofing material which is permanent in character and which cannot be removed by washing, weathering, or by the solvents used in-dry cleaning or by reaction of weather conditions, as it is permanent.
Another object is to provide a fireproofing material of such efficiency that relatively, small amounts of it will prove adequate for fireproofing and thus accomplish a saving in total weight of fireproofed material.
A further object is to provide a fireproofing agent which is non-corrosive and non-toxic, so that the agent itself and the material which has been treated with it can be freely and safely handled. 7
Other objects will appear from time to time throughout the specification'and claims.
A variety of fireproofing materials are now known and most of such materials have generally one or more of the following defects: They are ineificient and substantial weights are required. They are corrosive and toxic. They are not permanent in character.
It is present practice to apply by painting or otherwise relatively large amounts of metallic oxides as fireproofing agents. Among such oxides are those of tin, aluminum and antimony. Be cause each of these is relatively in'eificient, extremely large amounts are necessary to produce efl'ective fireproofing results. In the case of an-' timony oxide, which is probably the most efllcient, the weight which must be added to an ar ticle for fireproofing will be of the order of 50% of the weight of the article itself. Thus if a piece of canvas or tarpaulin or some other article untreated has a weight of 100 lbs. its weight will be 150 lbs. after treatment with antimony oxide. Antimony oxide" has the rather disad vantage that it, like arsenic oxide, is a cmnula'a 11Claims. (Cl. 26029.2)
tive poison and elaborate precautions must be taken in producing the material and in using it, and thus, also, materials which have been treated with antimony oxide are toxic and must be handled with extreme caution.
Another class of fireprooflng materials includes chlorinated waxes and resins which may be used along with or in combination with various metallic oxides for fireproofing. In the case of these materials also large quantities are required for efiectiveness and they have the further disadvantage that they are corrosive in character and form hydrochloric acid, particularly at elevated temperatures.
The firperoofing material of the present inven-' tion comprises the amides, imidesg d ii nidoamides of phosphoric ari'd thi'ophbs'phoric acids, as Well as the nitride of phosphoric acid. Tests have shown that these materials are excellent fire and flameproofing agents and that they are effective in very much smalleramounts than the metallic oxides used at present, such as the oxides of tin, aluminum and antimony. They have the further advantage that they are non-poisonous and non-corrosive and that they are insoluble in water and in most available solvents.
Phosphoric acid may be given the following structural formula:
OH O=POH 0H In this material it is possible to substitute ammonia for the three hydroxy groups by treating phosphoryltrichloride with dry ammonia and forming thus the triamide of phosphoric acid which has the following structural formula:
NH; 0=PNH2 NHa This latter material is usually known as phosphorylimidoamide and comprises a White powder insoluble in water and acids and only very slightl3 ailec'tedloy hot alkalies gpgn heati dtherr/whg phosphorylimidoamide loses a molecule of ammonia and the compound O=P=N is formed.
' This material is phosphorylnitride and comprises a white inert powder which forms a black glass at red heat.
In practice the fireproofing material of this invention is the water insoluble, chlorine free,
reaction product of phosphorus oxychloride with anhydrous ammonia. This reaction product consists of a mixture of phosphoryltriamide, phosphorylimidoamide and polyphosphorylamides. It ispossible, though very difficult, to separate the three components of the reaction product, but for the purpose of this invention it is not necessary since all three are powerful fireproofing agents. On the other hand, it is readily possible to control the proportion in which they are formed by controlling the conditions of the reaction; for example, when the reaction is affected at low temperatures, the phosphoryltriamide predominates in the reaction product, while higher temperatures favor the formation of the prosphorylimidoamide and polyphosphorylamides.
The existence of the polyphosphorylamides in the reaction described is indicated by results of experiments carried out by the inventors which do not pertain to the present invention. The evidence is not conclusive but indicative of their possible existence. The formation of the phosphoryltriamide and phosphorylimidoamide in the reaction oi. phosphorus oxychloride and anhydrous ammonia is a matter of record in the known technical literature. The differences discussed in the literature on the subject are further resolved by the assumption of the existence of the polyphosphorylamides. A probable structure for the polymeric amide may be:
P il l l vat mere H H H 'H The mixture of phosphoric acid amides which was just described. and which the inventors use as the fireproofing agent is a white amorphous inert material completely water insoluble. Mellor in his Authoritative Treatise of Inorganic Chemistry substantiates this view. 7
For the purpose of brevity the generic term phosphorylamides will be used throughout the specification and claims to indicate the mixture of phosphoric acid amides which is the reaction product of phosphorus oxychloride and anhydrous ammonia, as described above.
It is recognized today that fireproofing may be accomplished as a result of two actions: (1) the formation, upon heating, of a fire quenching gas such as ammonia, carbon dioxide or chlorine, which gas smothers the flame; and (2) the formation, upon heating, of a melted material which covers the combustible fibers or article and prevents burning.
The metallic oxides and some salts such as borax operate in the latter manner to produce, upon melting, a glass-like material. The ammonia and chlorine compounds act in the former manner to produce fire quenching gases.
The amides and imides of phosphoric and thiophosphoric acid are extremely effective because they partake of both methods of quenching fire. Upon heating a fire quenching gas is formed and also a glass-like material is produced as a result of melting, and this material covers the fibers or 7 f with Wbib. 1? i 2 ieqa qp e ts l 4 burning. The phosphorylnitride acts in the same way.
The following examples illustrate several uses of the material above described. The examples are given merely as typical of various uses and the invention is not limited to the particular examples given.
e Parts Phosphorylamides 30 Polyvinyl chloride 3 Acetone 67 Pentachlorphenol 0.1
Parts Phosphorylamides 25 Water Chlorinated paraflin 15. Light petroleum'solvent 8 Emulsifier 2 In this case the phosphorylamides are suspended in the water-in-oil emulsion from which they are applied on the material to be treated by spraying, dipping orroller coating. The chlorinated paraflin acts as a binder and since it is thermally unstable and upon decomposition hydrochloric acid is vformed, it further enhances the fireproofing quality of the mixture.
I III l 7 Parts Phosphorylamides 15 Water 25 Polyvinylchloride acetate copolymer 5 Dichlorethane 45 ilricresylphgephate 8 Eiifii ifier1 2 Here the vehicle for the phosphorylamides is an oil-in-Water emulsion. The binder is plasticized with tricresylphosphate, and both contribute to the fireproofing quality of the deposit.
' Parts Phosphorylamides 20 Water 45 Chlorinated naphthalene 10 Carbon tetrachloride 23 Emulsifier 2 This is another example of an oil-in-water emulsion using chlorinated napthalene as the thermally'unstable binder. The solvent used makes this emulsion safe to handle. In the same manner, other thermally unstable chlorinated organic compounds suitable as binders for the phosphorylamides can also be used. These could be neoprene, pentachlorobiphenyl, chlorinated, natural 70 or synthetic rubber, and chloropolystyrene.
r vParts Phosphorylamides 70 7.5, Chlorinated rubber w i a assesses An intimate mixtu-re of the two materials in fine powder form is dusted directly upon the fibers to be fireproofed. These are then h eated electronically to a temperature just high enough to soften the binder and thus fix the phosphorylamides permanently on the fibers. A slightpremoistening of the fibers with an atomized plasticizer like tricres-ylphosphite helps settle the powders and also flexibilize the deposit. "Thephosphite, in addition, inhibits hydrochloric acid formation. f
Parts Powdered phosphorylamides 75 Powdered polyvinylchloride acetate copolymer 25 This is another example of dry binding by means of heat.
The phosphorylamides, because of their nature, are preferably used with a binder. As indicated by the examples enumeratedabove,"thermally unstable chlorinated organic compounds v.are preferred because they are noncombustible. This should not be presumed to exclude other binders.
VII
Parts Phosphorylamides -I 50 Commercial polyvinyl acetate emulsion 45 Tricresylphosphate The polyvinyl acetate film alone supports fire but in the presence of the phosphorylamides it does not burn. On the other hand, the total effectiveness as a fireproofing mixture is much les than that of any of Examples I--VII, and the use of binders which support fire is recommended only when other considerations prevent the use of the thermally unstable chlorinated binders. Other film forming, water insoluble materials (or such as can be rendered water insoluble) may also be used. Among these are polystyrene emulsion, synthetic and natural latexes, and alkyd resin emulsions.
Examples VIII, IX and X illustrate the use of the phosphorylamides in typical fireproof surface coatings. Example VIII is a fireproof enamel; Example IX a fireproof paint; and Example X a fireproof lacquer.
The examples of surface coatings given above llO mer y ex ress. apic l suitable .PIPBQ P J LJE.
general a flameproof surface coating may be made in which the phosphorylamides constitute from 15% to 50% of the paint. The pigments used in these fireproof surface coatings are those normally used in the paint industry. Their choice depends upon the purpose they are to serve in the surface coating, andthey are generally chosen from the group of inorganic metallic oxides, carbonates, sulphides and sulphates such as titanium dioxide, lithopone, lead oxides and zinc oxides.
It is alsopossible to treat fibers, fabric sgetc in such a manner that the phosphorylamides are formed within and upon them. The reactants, dry gaseous ammonia and vapors of phosphoryltrichloride, are brought tog-ether upon the material to be treated wherein they react and deposit the phosphorylamides in and upon the material.
It should be pointed out, however, that even in this extreme case when the reaction takes place upon the fibers to deposit the fireproofing agents, there is nochemical interaction between the fibers and the phosphorylamides, andv the deposition is purely a physical one. No attemptis being made here, for example, to bringabou't chemical combination between the fibers and the reactants, and none takes place.
The materials treated by the products above mentioned have beenreferred to as being fireproofed. The result of the treatment is to make these materials greprg of and gam eproof. and also glowprop f, That is to say, the material treated,
when exposed in air to a flame, may be slowly consumed but if consumed no flame or glow is present, and the material itself will not support combustion. The absence of glow is important, because a glowing material which may be consumed without flame may nonetheless spread fire as a result of this glow by contact with untreated materials.
Any material, whether fiat goods, fibers or batting, when treated by any of the combinations of the examples given, becomes distinct and can readily be identified chemically as being fireproofed by means of the phosphorylamides. This is possible because of the insolubility of the phosphorylamides in all solvents. It is therefore possible to remove the phosphorylamides from the treated material and eliminate all other interfering substances and identify chemically the phosphorylamides.
The amount of phosphorylamides necessary satisfactorily to fireproof such materials may be as little as 10% by weight of the material, irrespective of any contribution of the binder to the total fireproofing effect. It is to be remembered that the binders proposed herein are in some cases not fireproof or fire resistant in themselves. However, as much as of phosphorylamides may be added without detrimental effect on the treated materials. In usual practice the total of the solids add on of 20% to 30% is satisfactory. The phosphorylamides may be mixed with or applied to a material to be fireproofed in almost any manner, either as the material is made or processed or after it has been made.
This application is a continuation-in-part of our co-pending application Serial No. 633,532, filed December '7, 1945, now abandoned.
We claim:
1. A fireproofing paint comprising 20-50% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia and 80-50% of normal paint ingredients includll ,QPE PEEUE Q.EXQFQ? E 5 winder-I.-.
WWW-rm eases soon i7 2. A fireproofing paint comprising 20-50% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia and 80-50% of normal paint ingredients, including pigment, resin and solvent; a
3. A fireproofing composition comprising 20- 50% of the water insoluble reaction product of phosphorous oxychlorlde with anhydrous ammonia suspended in 80-50% of a solution of thermally unstable chlorinated organic compounds as a binder.
4. A fireproofing composition comprising 50- 90% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia intimately mixed with 50-10% of thermally unstable chlorinated organic compounds as a binder.
5. A fireproofiing composition comprising 20- 50% of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia suspende in'80-50% of a material selected from the group consisting of polyvinyl acetate emulsion, polystyrene emulsion, synthetic and natural rubber latexes and alkyd resin emulsion as binders.
6. An article of manufacture comprising a mass of fibrous material fireproofed by the addition of the water insoluble reaction product of phosphorous oxychloride with anhydrous ammonia in the proportion of 10-80% of the weight of the article.
"7. An article of manufacture comprising a mass of fibrous material fireproofed by the composition of claim 3. I
8. An article of manufacture comprising a mass of fibrous material fireproofed by the composition of claim 4.
9. An article of manufacture comprising a mass of fibrous material fireproofed by the composition of claim 5. Y
10. A glowproofingcomposition comprising polyvinyl chloride and the water insoluble reaction product of phosphoryl chloride with anhydrous ammonia.
11. A glowproofing composition comprising polyvinyl acetate and the water insoluble reaction product of phosphoryl chloride with anhydrous ammonia.
JOHN TRUHLARJ ATHAN A. PANTSIOS.
' REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number
Claims (1)
1. A FIRE PROOFING PAINT COMPRISING 20-50% OF THE WATER INSOLUBLE REACTION PRODUCT OF PHOSPHOROUS OXYCHLORIDE WITH ANHYDROUS AMMONIA AND 80-50% OF NORMAL PAINT INGREDIENTS INCLUDING A PIGMENT AND A VEHICLE AND A BINDER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83514A US2582181A (en) | 1949-03-25 | 1949-03-25 | Fireproofing compositions containing water-insoluble phosphorylamides, and articles fireproofed therewith |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83514A US2582181A (en) | 1949-03-25 | 1949-03-25 | Fireproofing compositions containing water-insoluble phosphorylamides, and articles fireproofed therewith |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2582181A true US2582181A (en) | 1952-01-08 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US83514A Expired - Lifetime US2582181A (en) | 1949-03-25 | 1949-03-25 | Fireproofing compositions containing water-insoluble phosphorylamides, and articles fireproofed therewith |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2582181A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2642405A (en) * | 1948-12-30 | 1953-06-16 | Monsanto Chemicals | Fire-retarding coating composition composed of nitrogen-phosphorus compound with an aldehyde resin |
| US2661341A (en) * | 1950-06-21 | 1953-12-01 | Monsanto Chemicals | Fire-resistant resinous product and process for producing same |
| US2676162A (en) * | 1949-06-28 | 1954-04-20 | Monsanto Chemicals | Fire retardant coating compositions containing a reaction product of phosphoryl chloride and anhydrous ammonia and articles coated therewith |
| US2816004A (en) * | 1951-06-30 | 1957-12-10 | Monsanto Chemicals | Cellulosic solutions containing fire retardant and method of extruding |
| US2949385A (en) * | 1953-01-27 | 1960-08-16 | Monsanto Chemicals | Fire-retardant process |
| US2980506A (en) * | 1956-09-27 | 1961-04-18 | Henkel & Compagnie G M B H | Nitrogen-phosphoric acid compounds containing active chlorine |
| US3093602A (en) * | 1958-08-05 | 1963-06-11 | Interchem Corp | Water-in-oil emulsion textile decorating compositions |
| US3449161A (en) * | 1965-08-09 | 1969-06-10 | Hooker Chemical Corp | Fire retardant intumescent coating compositions |
| US4063883A (en) * | 1974-08-20 | 1977-12-20 | Hoechst Aktiengesellschaft | Manufacture of flame-retardant regenerated cellulose fibres |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2052886A (en) * | 1933-05-16 | 1936-09-01 | Brick Trust Ltd | Treatment of various materials for rendering them impermeable and fireproof |
| US2163085A (en) * | 1938-09-15 | 1939-06-20 | Du Pont | Flameproofed cellulosic materials |
| US2378715A (en) * | 1942-05-28 | 1945-06-19 | Leatherman Martin | Fireproofing compositions |
| US2401440A (en) * | 1942-02-18 | 1946-06-04 | Monsanto Chemicals | Cellulose phosphonamides |
-
1949
- 1949-03-25 US US83514A patent/US2582181A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2052886A (en) * | 1933-05-16 | 1936-09-01 | Brick Trust Ltd | Treatment of various materials for rendering them impermeable and fireproof |
| US2163085A (en) * | 1938-09-15 | 1939-06-20 | Du Pont | Flameproofed cellulosic materials |
| US2401440A (en) * | 1942-02-18 | 1946-06-04 | Monsanto Chemicals | Cellulose phosphonamides |
| US2378715A (en) * | 1942-05-28 | 1945-06-19 | Leatherman Martin | Fireproofing compositions |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2642405A (en) * | 1948-12-30 | 1953-06-16 | Monsanto Chemicals | Fire-retarding coating composition composed of nitrogen-phosphorus compound with an aldehyde resin |
| US2676162A (en) * | 1949-06-28 | 1954-04-20 | Monsanto Chemicals | Fire retardant coating compositions containing a reaction product of phosphoryl chloride and anhydrous ammonia and articles coated therewith |
| US2661341A (en) * | 1950-06-21 | 1953-12-01 | Monsanto Chemicals | Fire-resistant resinous product and process for producing same |
| US2816004A (en) * | 1951-06-30 | 1957-12-10 | Monsanto Chemicals | Cellulosic solutions containing fire retardant and method of extruding |
| US2949385A (en) * | 1953-01-27 | 1960-08-16 | Monsanto Chemicals | Fire-retardant process |
| US2980506A (en) * | 1956-09-27 | 1961-04-18 | Henkel & Compagnie G M B H | Nitrogen-phosphoric acid compounds containing active chlorine |
| US3093602A (en) * | 1958-08-05 | 1963-06-11 | Interchem Corp | Water-in-oil emulsion textile decorating compositions |
| US3449161A (en) * | 1965-08-09 | 1969-06-10 | Hooker Chemical Corp | Fire retardant intumescent coating compositions |
| US4063883A (en) * | 1974-08-20 | 1977-12-20 | Hoechst Aktiengesellschaft | Manufacture of flame-retardant regenerated cellulose fibres |
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