CA2461872C - Formulations ameliorees permettant de neutraliser des substances toxiques chimiques, biologiques et industrielles - Google Patents
Formulations ameliorees permettant de neutraliser des substances toxiques chimiques, biologiques et industrielles Download PDFInfo
- Publication number
- CA2461872C CA2461872C CA2461872A CA2461872A CA2461872C CA 2461872 C CA2461872 C CA 2461872C CA 2461872 A CA2461872 A CA 2461872A CA 2461872 A CA2461872 A CA 2461872A CA 2461872 C CA2461872 C CA 2461872C
- Authority
- CA
- Canada
- Prior art keywords
- formulation
- water
- reactive compound
- combination
- bleaching activator
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 201
- 238000009472 formulation Methods 0.000 title claims abstract description 175
- 238000006386 neutralization reaction Methods 0.000 title claims description 20
- 239000000126 substance Substances 0.000 title abstract description 26
- 239000012190 activator Substances 0.000 claims abstract description 102
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 81
- 229910001868 water Inorganic materials 0.000 claims abstract description 81
- 238000004061 bleaching Methods 0.000 claims abstract description 79
- 150000001875 compounds Chemical class 0.000 claims abstract description 77
- 239000002904 solvent Substances 0.000 claims abstract description 25
- 230000003381 solubilizing effect Effects 0.000 claims abstract description 15
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 91
- UYAAVKFHBMJOJZ-UHFFFAOYSA-N diimidazo[1,3-b:1',3'-e]pyrazine-5,10-dione Chemical compound O=C1C2=CN=CN2C(=O)C2=CN=CN12 UYAAVKFHBMJOJZ-UHFFFAOYSA-N 0.000 claims description 64
- 229940116423 propylene glycol diacetate Drugs 0.000 claims description 64
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 claims description 48
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 42
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 39
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 claims description 32
- 239000007787 solid Substances 0.000 claims description 31
- 239000003093 cationic surfactant Substances 0.000 claims description 29
- 239000004615 ingredient Substances 0.000 claims description 26
- 239000011736 potassium bicarbonate Substances 0.000 claims description 26
- 235000015497 potassium bicarbonate Nutrition 0.000 claims description 26
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims description 26
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 26
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 claims description 24
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 24
- 229940045872 sodium percarbonate Drugs 0.000 claims description 24
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 22
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 20
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims description 20
- 125000002091 cationic group Chemical group 0.000 claims description 19
- 150000005323 carbonate salts Chemical class 0.000 claims description 16
- 241000282372 Panthera onca Species 0.000 claims description 14
- 239000003752 hydrotrope Substances 0.000 claims description 13
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 12
- 150000002191 fatty alcohols Chemical class 0.000 claims description 12
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 claims description 12
- KMZHZAAOEWVPSE-UHFFFAOYSA-N 2,3-dihydroxypropyl acetate Chemical compound CC(=O)OCC(O)CO KMZHZAAOEWVPSE-UHFFFAOYSA-N 0.000 claims description 11
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 claims description 11
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 11
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 11
- JUGOREOARAHOCO-UHFFFAOYSA-M acetylcholine chloride Chemical compound [Cl-].CC(=O)OCC[N+](C)(C)C JUGOREOARAHOCO-UHFFFAOYSA-M 0.000 claims description 11
- 229960004266 acetylcholine chloride Drugs 0.000 claims description 11
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 claims description 11
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 11
- 235000011181 potassium carbonates Nutrition 0.000 claims description 11
- LHZYNHLHHRQGOX-UHFFFAOYSA-N dihydroperoxy carbonate Chemical compound OOOC(=O)OOO LHZYNHLHHRQGOX-UHFFFAOYSA-N 0.000 claims description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 8
- 239000001099 ammonium carbonate Substances 0.000 claims description 8
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 8
- 229960001922 sodium perborate Drugs 0.000 claims description 8
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 claims description 8
- WODGXFMUOLGZSY-UHFFFAOYSA-J tetrasodium phosphonatooxy phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OOP([O-])([O-])=O WODGXFMUOLGZSY-UHFFFAOYSA-J 0.000 claims description 8
- KJFGIEUERFWKMN-UHFFFAOYSA-M tetrasodium trioxido(oxidooxy)silane Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]O[Si]([O-])([O-])[O-] KJFGIEUERFWKMN-UHFFFAOYSA-M 0.000 claims description 8
- 229920003169 water-soluble polymer Polymers 0.000 claims description 8
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 7
- 239000004353 Polyethylene glycol 8000 Substances 0.000 claims description 6
- 229960000686 benzalkonium chloride Drugs 0.000 claims description 6
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims description 6
- 229940085678 polyethylene glycol 8000 Drugs 0.000 claims description 6
- 235000019446 polyethylene glycol 8000 Nutrition 0.000 claims description 6
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 claims description 4
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 235000012538 ammonium bicarbonate Nutrition 0.000 claims description 4
- 235000012501 ammonium carbonate Nutrition 0.000 claims description 4
- HQRPHMAXFVUBJX-UHFFFAOYSA-M lithium;hydrogen carbonate Chemical compound [Li+].OC([O-])=O HQRPHMAXFVUBJX-UHFFFAOYSA-M 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- ADCUEPOHPCPMCE-UHFFFAOYSA-N 4-cyanobenzoic acid Chemical compound OC(=O)C1=CC=C(C#N)C=C1 ADCUEPOHPCPMCE-UHFFFAOYSA-N 0.000 claims description 3
- 229920002594 Polyethylene Glycol 8000 Polymers 0.000 claims description 3
- 235000013773 glyceryl triacetate Nutrition 0.000 claims description 3
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims description 3
- 229960002622 triacetin Drugs 0.000 claims description 3
- AZUXKVXMJOIAOF-UHFFFAOYSA-N 1-(2-hydroxypropoxy)propan-2-ol Chemical compound CC(O)COCC(C)O AZUXKVXMJOIAOF-UHFFFAOYSA-N 0.000 claims description 2
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 2
- 229920002907 Guar gum Polymers 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 claims description 2
- 229960001950 benzethonium chloride Drugs 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 claims description 2
- 229960001927 cetylpyridinium chloride Drugs 0.000 claims description 2
- 150000001805 chlorine compounds Chemical class 0.000 claims description 2
- 239000000665 guar gum Substances 0.000 claims description 2
- 229960002154 guar gum Drugs 0.000 claims description 2
- 235000010417 guar gum Nutrition 0.000 claims description 2
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 claims description 2
- 229920002401 polyacrylamide Polymers 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 150000005217 methyl ethers Chemical class 0.000 claims 1
- 238000010944 pre-mature reactiony Methods 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 44
- -1 CW and BW compounds Chemical class 0.000 abstract description 30
- 231100000331 toxic Toxicity 0.000 abstract description 10
- 230000002588 toxic effect Effects 0.000 abstract description 10
- 230000002411 adverse Effects 0.000 abstract description 6
- 239000003317 industrial substance Substances 0.000 abstract description 6
- 230000008821 health effect Effects 0.000 abstract description 5
- 231100000252 nontoxic Toxicity 0.000 abstract description 5
- 230000003000 nontoxic effect Effects 0.000 abstract description 5
- 230000009972 noncorrosive effect Effects 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 50
- 239000006260 foam Substances 0.000 description 47
- 238000012360 testing method Methods 0.000 description 43
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 39
- 239000000243 solution Substances 0.000 description 37
- 239000013043 chemical agent Substances 0.000 description 34
- 210000004215 spore Anatomy 0.000 description 31
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 30
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 30
- 241000219198 Brassica Species 0.000 description 27
- 235000003351 Brassica cretica Nutrition 0.000 description 27
- 235000003343 Brassica rupestris Nutrition 0.000 description 27
- 238000005202 decontamination Methods 0.000 description 27
- 230000003588 decontaminative effect Effects 0.000 description 27
- 235000010460 mustard Nutrition 0.000 description 27
- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 26
- 241000193738 Bacillus anthracis Species 0.000 description 25
- 239000007800 oxidant agent Substances 0.000 description 24
- 230000001590 oxidative effect Effects 0.000 description 24
- 238000006243 chemical reaction Methods 0.000 description 22
- 238000000034 method Methods 0.000 description 22
- 150000002978 peroxides Chemical class 0.000 description 21
- 239000002002 slurry Substances 0.000 description 20
- 238000002156 mixing Methods 0.000 description 18
- 230000007797 corrosion Effects 0.000 description 17
- 238000005260 corrosion Methods 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 239000003112 inhibitor Substances 0.000 description 15
- 239000007788 liquid Substances 0.000 description 15
- 235000017557 sodium bicarbonate Nutrition 0.000 description 15
- 239000000872 buffer Substances 0.000 description 13
- 244000063299 Bacillus subtilis Species 0.000 description 12
- 235000014469 Bacillus subtilis Nutrition 0.000 description 12
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 10
- 239000003599 detergent Substances 0.000 description 10
- 239000008258 liquid foam Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000000470 constituent Substances 0.000 description 9
- 229920001223 polyethylene glycol Polymers 0.000 description 9
- 239000003124 biologic agent Substances 0.000 description 8
- 239000013020 final formulation Substances 0.000 description 8
- 230000009467 reduction Effects 0.000 description 8
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000006227 byproduct Substances 0.000 description 7
- 230000006378 damage Effects 0.000 description 7
- 239000011929 di(propylene glycol) methyl ether Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 6
- 241000607479 Yersinia pestis Species 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 238000001514 detection method Methods 0.000 description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 4
- 239000004348 Glyceryl diacetate Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000994 depressogenic effect Effects 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 235000019443 glyceryl diacetate Nutrition 0.000 description 4
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 239000005949 Malathion Substances 0.000 description 3
- AOMUHOFOVNGZAN-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
- DYAHQFWOVKZOOW-UHFFFAOYSA-N Sarin Chemical compound CC(C)OP(C)(F)=O DYAHQFWOVKZOOW-UHFFFAOYSA-N 0.000 description 3
- 239000001083 [(2R,3R,4S,5R)-1,2,4,5-tetraacetyloxy-6-oxohexan-3-yl] acetate Substances 0.000 description 3
- UAOKXEHOENRFMP-ZJIFWQFVSA-N [(2r,3r,4s,5r)-2,3,4,5-tetraacetyloxy-6-oxohexyl] acetate Chemical compound CC(=O)OC[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)C=O UAOKXEHOENRFMP-ZJIFWQFVSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 229920006317 cationic polymer Polymers 0.000 description 3
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 3
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 3
- 230000008014 freezing Effects 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 239000003906 humectant Substances 0.000 description 3
- 229960000453 malathion Drugs 0.000 description 3
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 231100000419 toxicity Toxicity 0.000 description 3
- 230000001988 toxicity Effects 0.000 description 3
- UZJXHJFKUSBWEL-UHFFFAOYSA-N 2,3,3-trimethylbutylphosphonic acid Chemical compound CC(C)(C)C(C)CP(O)(O)=O UZJXHJFKUSBWEL-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 2
- UXDDRFCJKNROTO-UHFFFAOYSA-N Glycerol 1,2-diacetate Chemical compound CC(=O)OCC(CO)OC(C)=O UXDDRFCJKNROTO-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 125000003047 N-acetyl group Chemical group 0.000 description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- GRXKLBBBQUKJJZ-UHFFFAOYSA-N Soman Chemical compound CC(C)(C)C(C)OP(C)(F)=O GRXKLBBBQUKJJZ-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 230000001154 acute effect Effects 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000002528 anti-freeze Effects 0.000 description 2
- 210000004666 bacterial spore Anatomy 0.000 description 2
- 239000002575 chemical warfare agent Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000006184 cosolvent Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- UFZOPKFMKMAWLU-UHFFFAOYSA-N ethoxy(methyl)phosphinic acid Chemical compound CCOP(C)(O)=O UFZOPKFMKMAWLU-UHFFFAOYSA-N 0.000 description 2
- 239000013505 freshwater Substances 0.000 description 2
- 229940051250 hexylene glycol Drugs 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 239000012038 nucleophile Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- QDXIHHOPZFCEAP-UHFFFAOYSA-N 2-chloroethylsulfanylbenzene Chemical compound ClCCSC1=CC=CC=C1 QDXIHHOPZFCEAP-UHFFFAOYSA-N 0.000 description 1
- LTALJGSZILUUQA-UHFFFAOYSA-N 2-nonanoyloxybenzenesulfonic acid Chemical compound CCCCCCCCC(=O)OC1=CC=CC=C1S(O)(=O)=O LTALJGSZILUUQA-UHFFFAOYSA-N 0.000 description 1
- 108010053481 Antifreeze Proteins Proteins 0.000 description 1
- 108030001720 Bontoxilysin Proteins 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 0 C=*C1CCCC1 Chemical compound C=*C1CCCC1 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
- 239000012028 Fenton's reagent Substances 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- OVRNDRQMDRJTHS-UHFFFAOYSA-N N-acelyl-D-glucosamine Natural products CC(=O)NC1C(O)OC(CO)C(O)C1O OVRNDRQMDRJTHS-UHFFFAOYSA-N 0.000 description 1
- OVRNDRQMDRJTHS-FMDGEEDCSA-N N-acetyl-beta-D-glucosamine Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 description 1
- MBLBDJOUHNCFQT-LXGUWJNJSA-N N-acetylglucosamine Natural products CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO MBLBDJOUHNCFQT-LXGUWJNJSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 206010035148 Plague Diseases 0.000 description 1
- MLHOXUWWKVQEJB-UHFFFAOYSA-N Propyleneglycol diacetate Chemical group CC(=O)OC(C)COC(C)=O MLHOXUWWKVQEJB-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- BHIIGRBMZRSDRI-UHFFFAOYSA-N [chloro(phenoxy)phosphoryl]oxybenzene Chemical compound C=1C=CC=CC=1OP(=O)(Cl)OC1=CC=CC=C1 BHIIGRBMZRSDRI-UHFFFAOYSA-N 0.000 description 1
- PJVJTCIRVMBVIA-JTQLQIEISA-N [dimethylamino(ethoxy)phosphoryl]formonitrile Chemical compound CCO[P@@](=O)(C#N)N(C)C PJVJTCIRVMBVIA-JTQLQIEISA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- VDEUYMSGMPQMIK-UHFFFAOYSA-N benzhydroxamic acid Chemical compound ONC(=O)C1=CC=CC=C1 VDEUYMSGMPQMIK-UHFFFAOYSA-N 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- 229940053031 botulinum toxin Drugs 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 231100000481 chemical toxicant Toxicity 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- ZFAKTZXUUNBLEB-UHFFFAOYSA-N dicyclohexylazanium;nitrite Chemical compound [O-]N=O.C1CCCCC1[NH2+]C1CCCCC1 ZFAKTZXUUNBLEB-UHFFFAOYSA-N 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000003889 eye drop Substances 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- MGZTXXNFBIUONY-UHFFFAOYSA-N hydrogen peroxide;iron(2+);sulfuric acid Chemical compound [Fe+2].OO.OS(O)(=O)=O MGZTXXNFBIUONY-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- NBTOZLQBSIZIKS-UHFFFAOYSA-N methoxide Chemical compound [O-]C NBTOZLQBSIZIKS-UHFFFAOYSA-N 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 229950006780 n-acetylglucosamine Drugs 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 239000006174 pH buffer Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- FHHJDRFHHWUPDG-UHFFFAOYSA-L peroxysulfate(2-) Chemical compound [O-]OS([O-])(=O)=O FHHJDRFHHWUPDG-UHFFFAOYSA-L 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 230000009295 sperm incapacitation Effects 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- SPALIFXDWQTXKS-UHFFFAOYSA-M tetrapentylazanium;bromide Chemical compound [Br-].CCCCC[N+](CCCCC)(CCCCC)CCCCC SPALIFXDWQTXKS-UHFFFAOYSA-M 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- HXJAYEBLPWXZLI-UHFFFAOYSA-M triacetyl(methyl)azanium;bromide Chemical compound [Br-].CC(=O)[N+](C)(C(C)=O)C(C)=O HXJAYEBLPWXZLI-UHFFFAOYSA-M 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D3/00—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances
- A62D3/30—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D3/00—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances
- A62D3/30—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents
- A62D3/38—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents by oxidation; by combustion
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D3/00—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances
- A62D3/30—Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents
- A62D3/36—Detoxification by using acid or alkaline reagents
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2101/00—Harmful chemical substances made harmless, or less harmful, by effecting chemical change
- A62D2101/02—Chemical warfare substances, e.g. cholinesterase inhibitors
Landscapes
- Business, Economics & Management (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Management (AREA)
- Detergent Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fire-Extinguishing Compositions (AREA)
Abstract
L'invention concerne une formulation améliorée et un procédé de fabrication permettant de neutraliser les effets nocifs pour la santé de composés à la fois chimiques et biologiques, en particulier des agents de guerre chimique (CW) et de guerre biologique (BW) et des produits chimiques industriels toxiques. Cette formulation améliorée de l'invention est non toxique et non corrosive, et peut être administrée par le biais d'une variété de moyens, et en différentes phases. Cette formulation contient des composés de solubilisation susceptibles d'attaquer de manière efficace les composés chimiques et biologiques, en particulier les composés CW et BW, et au moins un composé réactif servant à attaquer (et à détoxifier ou à supprimer) ce composé. Cette formulation comprend au moins un agent de solubilisation, un composé réactif, un activateur de blanchiment et de l'eau.
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32650801P | 2001-10-01 | 2001-10-01 | |
| US60/326,508 | 2001-10-01 | ||
| US33427101P | 2001-11-30 | 2001-11-30 | |
| US60/334,271 | 2001-11-30 | ||
| US38710402P | 2002-06-07 | 2002-06-07 | |
| US60/387,104 | 2002-06-07 | ||
| PCT/US2002/029886 WO2003028429A2 (fr) | 2001-10-01 | 2002-09-20 | Formulations ameliorees permettant de neutraliser des substances toxiques chimiques, biologiques et industrielles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2461872A1 CA2461872A1 (fr) | 2003-04-10 |
| CA2461872C true CA2461872C (fr) | 2013-11-26 |
Family
ID=27406465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2461872A Expired - Lifetime CA2461872C (fr) | 2001-10-01 | 2002-09-20 | Formulations ameliorees permettant de neutraliser des substances toxiques chimiques, biologiques et industrielles |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP1434625B1 (fr) |
| JP (1) | JP4582514B2 (fr) |
| KR (1) | KR100916328B1 (fr) |
| CN (1) | CN1612766B (fr) |
| AU (1) | AU2002341750B2 (fr) |
| BR (1) | BR0213019B1 (fr) |
| CA (1) | CA2461872C (fr) |
| EA (1) | EA009242B1 (fr) |
| HK (1) | HK1073618A1 (fr) |
| IL (2) | IL161200A0 (fr) |
| MX (1) | MXPA04003037A (fr) |
| WO (1) | WO2003028429A2 (fr) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006076334A1 (fr) * | 2005-01-11 | 2006-07-20 | Clean Earth Technologies, Llc | Compositions de peracides/peroxydes et utilisation de ces compositions en tant qu'agents antimicrobiens et photosensibilisants |
| WO2006076406A2 (fr) * | 2005-01-11 | 2006-07-20 | Clean Earth Technologies, Llc | Formulations destinees a la decontamination de produits chimiques toxiques |
| US9724550B2 (en) | 2006-08-15 | 2017-08-08 | American Sterilizer Company | One part, solids containing decontamination blend composition |
| US9700644B2 (en) | 2006-08-15 | 2017-07-11 | American Sterilizer Company | One part, solids containing decontamination blend composition |
| US20120141598A1 (en) * | 2008-10-08 | 2012-06-07 | Jessie Kater | Broad spectrum decontaminate and dispersement system |
| US8969283B2 (en) * | 2009-02-05 | 2015-03-03 | American Sterilizer Company | Low odor, hard surface sporicides and chemical decontaminants |
| RU2484868C2 (ru) * | 2009-04-24 | 2013-06-20 | Ольга Анатольевна Афанасьевская | Комплексная, безотходная переработка токсичных отходов |
| US20110177145A1 (en) * | 2009-07-27 | 2011-07-21 | E.I. Du Pont De Nemours And Company | In situ preparation of peracid-based removable antimicrobial coating compositions and methods of use |
| GB201010374D0 (en) | 2010-06-21 | 2010-08-04 | Mtp Innovations Ltd | Disinfectant composition |
| WO2016040230A1 (fr) * | 2014-09-09 | 2016-03-17 | Lonza, Inc. | Composition désinfectante contenant des composés d'ammonium quaternaire |
| EA026955B1 (ru) * | 2015-03-16 | 2017-06-30 | Общество с ограниченной ответственностью "ФАРМА-ПОКРОВ" | Дезинфицирующая композиция |
| JP6639099B2 (ja) * | 2015-03-24 | 2020-02-05 | 花王株式会社 | 酸化性組成物 |
| EP4011210A1 (fr) * | 2015-07-17 | 2022-06-15 | Next Science IP Holdings Pty Ltd | Utilisation d'une composition antimicrobienne efficace contre les endospores |
| JP7102008B2 (ja) * | 2017-06-15 | 2022-07-19 | ディコン７ システムズ インク | 浄化製剤 |
| CN110913960A (zh) * | 2017-07-17 | 2020-03-24 | 蒂艾克思股份有限公司 | 中和组合物及其使用方法 |
| MX2020007668A (es) * | 2018-01-17 | 2020-11-24 | Decon7 Systems Inc | Formulación para descontaminación de superficies. |
| CN110150279B (zh) * | 2019-06-03 | 2023-08-25 | 南通思锐生物科技有限公司 | 一种即时快速生成过氧乙酸消毒剂的配制方法 |
| CN111388935B (zh) * | 2020-04-29 | 2021-10-01 | 中国人民解放军陆军防化学院 | 一种耐低温泡沫洗消剂及其制备方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US366A (en) * | 1837-08-31 | Quadrant hinge foe | ||
| US3810788A (en) * | 1966-02-15 | 1974-05-14 | P Steyermark | Method for decontaminating chemical warfare agents |
| US3852210A (en) * | 1972-08-11 | 1974-12-03 | Flow Pharma Inc | Stable liquid detergent concentrates containing active oxygen |
| JPS526867B2 (fr) * | 1972-09-14 | 1977-02-25 | ||
| GB8304990D0 (en) * | 1983-02-23 | 1983-03-30 | Procter & Gamble | Detergent ingredients |
| JPH0617289B2 (ja) * | 1985-12-27 | 1994-03-09 | エーザイ株式会社 | 蓄舎用殺菌剤組成物 |
| JPS6390586A (ja) * | 1986-09-29 | 1988-04-21 | リ−・フア−マス−テイカルズ・インコ−ポレイテツド | 改良された接着タブ系 |
| USH366H (en) * | 1987-03-18 | 1987-11-03 | The United States Of America As Represented By The Secretary Of The Army | Microemulsions containing sulfolanes |
| US4850729A (en) * | 1987-04-07 | 1989-07-25 | David N. Kramer | Decontaminating composition and delivery system therefor |
| US5387717A (en) * | 1992-08-12 | 1995-02-07 | Buckman Laboratories International, Inc. | Method for the detoxification of mustard gas, sulfur-containing quaternary ammonium ionene polymers and their use as microbicides |
| US5421906A (en) * | 1993-04-05 | 1995-06-06 | Enclean Environmental Services Group, Inc. | Methods for removal of contaminants from surfaces |
| US5760089A (en) * | 1996-03-13 | 1998-06-02 | The United States Of America As Represented By The Secretary Of The Navy | Chemical warfare agent decontaminant solution using quaternary ammonium complexes |
| JP4498475B2 (ja) * | 1996-06-26 | 2010-07-07 | 花王株式会社 | 液体漂白剤組成物 |
| JPH1088192A (ja) * | 1996-09-10 | 1998-04-07 | Sekisui Chem Co Ltd | 漂白洗浄剤組成物 |
| FR2766725A1 (fr) * | 1997-07-31 | 1999-02-05 | Irdec Sa | Compositions decontaminantes stabilisees |
| FR2766724B1 (fr) | 1997-07-31 | 1999-10-22 | Irdec Sa | Compositions decontaminantes non agressives |
| US6245957B1 (en) * | 1999-09-02 | 2001-06-12 | The United States Of America As Represented By The Secretary Of The Army | Universal decontaminating solution for chemical warfare agents |
| ES2312419T3 (es) * | 2000-02-23 | 2009-03-01 | THE PROCTER & GAMBLE COMPANY | Composiciones detergentes para lavar la ropa granuladas que comprenden poliamidas de ion hibrido. |
-
2002
- 2002-09-20 EP EP02775899.4A patent/EP1434625B1/fr not_active Expired - Lifetime
- 2002-09-20 EA EA200400500A patent/EA009242B1/ru not_active IP Right Cessation
- 2002-09-20 WO PCT/US2002/029886 patent/WO2003028429A2/fr active Application Filing
- 2002-09-20 JP JP2003531785A patent/JP4582514B2/ja not_active Expired - Lifetime
- 2002-09-20 KR KR1020047004858A patent/KR100916328B1/ko active IP Right Grant
- 2002-09-20 CA CA2461872A patent/CA2461872C/fr not_active Expired - Lifetime
- 2002-09-20 BR BRPI0213019-0A patent/BR0213019B1/pt not_active IP Right Cessation
- 2002-09-20 CN CN028241258A patent/CN1612766B/zh not_active Expired - Lifetime
- 2002-09-20 AU AU2002341750A patent/AU2002341750B2/en not_active Expired
- 2002-09-20 MX MXPA04003037A patent/MXPA04003037A/es active IP Right Grant
- 2002-09-20 IL IL16120002A patent/IL161200A0/xx active IP Right Grant
-
2004
- 2004-03-31 IL IL161200A patent/IL161200A/en unknown
-
2005
- 2005-08-31 HK HK05107631.5A patent/HK1073618A1/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003028429A2 (fr) | 2003-04-10 |
| IL161200A0 (en) | 2004-08-31 |
| EP1434625A2 (fr) | 2004-07-07 |
| IL161200A (en) | 2007-09-20 |
| KR100916328B1 (ko) | 2009-09-11 |
| BR0213019A (pt) | 2004-10-05 |
| HK1073618A1 (en) | 2005-10-14 |
| AU2002341750B2 (en) | 2007-10-11 |
| EP1434625B1 (fr) | 2018-07-18 |
| MXPA04003037A (es) | 2005-07-01 |
| CN1612766B (zh) | 2010-10-13 |
| EA009242B1 (ru) | 2007-12-28 |
| CA2461872A1 (fr) | 2003-04-10 |
| EA200400500A1 (ru) | 2004-10-28 |
| WO2003028429A3 (fr) | 2003-12-18 |
| EP1434625A4 (fr) | 2010-07-21 |
| JP4582514B2 (ja) | 2010-11-17 |
| BR0213019B1 (pt) | 2011-12-27 |
| CN1612766A (zh) | 2005-05-04 |
| KR20040048923A (ko) | 2004-06-10 |
| JP2005504856A (ja) | 2005-02-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7282470B2 (en) | Decontamination formulation with sorbent additive | |
| US7390432B2 (en) | Enhanced formulations for neutralization of chemical, biological and industrial toxants | |
| CA2461872C (fr) | Formulations ameliorees permettant de neutraliser des substances toxiques chimiques, biologiques et industrielles | |
| WO2005055963A2 (fr) | Formulation de decontamination avec additif de sorption | |
| US7064241B2 (en) | Chemical and biological warfare decontaminating solution using peracids and germinants in microemulsions, process and product thereof | |
| US7271137B2 (en) | Decontamination formulations for disinfection and sterilization | |
| AU2002341750A1 (en) | Enhanced formulations for neutralization of chemical, biological and industrial toxants | |
| CA2300698C (fr) | Formulation de decontamination a large spectre et methode d'utilisation | |
| US20030060517A1 (en) | Concentrated formulations and methods for neutralizing chemical and biological toxants | |
| US8241562B1 (en) | Enhanced toxic cloud knockdown spray system for decontamination applications | |
| US7429556B2 (en) | Universal halide-enhanced decontaminating formulation | |
| US7662759B1 (en) | Decontamination formulation with additive for enhanced mold remediation | |
| US7531132B1 (en) | Chemical and biological warfare agent decontaminating methods using dioxirane producing formulations | |
| Tucker et al. | Decontamination formulation with sorbent additive | |
| TW589179B (en) | Enhanced formulations for neutralization of chemical, biological and industrial toxants | |
| Tucker | Granulated decontamination formulations |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKEX | Expiry |
Effective date: 20220920 |
|
| MKEX | Expiry |
Effective date: 20220920 |