IL144978A - Decontamination composition containing chloroisocyanuric acid, methods for the preparation thereof and kits containing the same - Google Patents
Decontamination composition containing chloroisocyanuric acid, methods for the preparation thereof and kits containing the sameInfo
- Publication number
- IL144978A IL144978A IL14497800A IL14497800A IL144978A IL 144978 A IL144978 A IL 144978A IL 14497800 A IL14497800 A IL 14497800A IL 14497800 A IL14497800 A IL 14497800A IL 144978 A IL144978 A IL 144978A
- Authority
- IL
- Israel
- Prior art keywords
- decontamination
- formulation
- surfactant
- buffer
- group
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 235
- 238000005202 decontamination Methods 0.000 title claims abstract description 137
- 230000003588 decontaminative effect Effects 0.000 title claims abstract description 126
- ISAOUZVKYLHALD-UHFFFAOYSA-N 1-chloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)NC(=O)NC1=O ISAOUZVKYLHALD-UHFFFAOYSA-N 0.000 title claims abstract description 19
- 238000000034 method Methods 0.000 title claims description 21
- 238000002360 preparation method Methods 0.000 title description 10
- 238000009472 formulation Methods 0.000 claims abstract description 157
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 112
- 239000004094 surface-active agent Substances 0.000 claims abstract description 111
- 239000006184 cosolvent Substances 0.000 claims abstract description 61
- 239000000872 buffer Substances 0.000 claims abstract description 53
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 52
- 239000000243 solution Substances 0.000 claims abstract description 45
- 229920001451 polypropylene glycol Polymers 0.000 claims abstract description 22
- 239000000126 substance Substances 0.000 claims abstract description 13
- CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical compound ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 claims description 55
- 125000000217 alkyl group Chemical group 0.000 claims description 34
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 239000007864 aqueous solution Substances 0.000 claims description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 14
- 229910052783 alkali metal Inorganic materials 0.000 claims description 14
- -1 alkali metal salt Chemical class 0.000 claims description 13
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 12
- 150000001412 amines Chemical class 0.000 claims description 12
- 150000001340 alkali metals Chemical class 0.000 claims description 11
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 11
- LWXVCCOAQYNXNX-UHFFFAOYSA-N lithium hypochlorite Chemical compound [Li+].Cl[O-] LWXVCCOAQYNXNX-UHFFFAOYSA-N 0.000 claims description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 8
- CDMADVZSLOHIFP-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 CDMADVZSLOHIFP-UHFFFAOYSA-N 0.000 claims description 8
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- 229920001223 polyethylene glycol Polymers 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 238000005273 aeration Methods 0.000 claims description 6
- 238000005187 foaming Methods 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000004185 ester group Chemical group 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- WDZLZBIKRZDKIE-UHFFFAOYSA-N ClN1C(N(C(C=2NC(NC1=2)=O)=O)[N+]#[C-])=O Chemical compound ClN1C(N(C(C=2NC(NC1=2)=O)=O)[N+]#[C-])=O WDZLZBIKRZDKIE-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 3
- 239000000337 buffer salt Substances 0.000 claims description 3
- 230000000593 degrading effect Effects 0.000 claims description 3
- 150000002334 glycols Chemical class 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- KEZYHIPQRGTUDU-UHFFFAOYSA-N 2-[dithiocarboxy(methyl)amino]acetic acid Chemical compound SC(=S)N(C)CC(O)=O KEZYHIPQRGTUDU-UHFFFAOYSA-N 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- KEAYESYHFKHZAL-IGMARMGPSA-N sodium-23 atom Chemical compound [23Na] KEAYESYHFKHZAL-IGMARMGPSA-N 0.000 claims 1
- 239000006260 foam Substances 0.000 abstract description 49
- 239000004480 active ingredient Substances 0.000 abstract description 46
- 238000006243 chemical reaction Methods 0.000 abstract description 19
- 230000002285 radioactive effect Effects 0.000 abstract description 19
- 230000007062 hydrolysis Effects 0.000 abstract description 18
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 18
- 239000012141 concentrate Substances 0.000 abstract description 13
- 239000004615 ingredient Substances 0.000 abstract description 13
- 230000000694 effects Effects 0.000 abstract description 12
- 230000003647 oxidation Effects 0.000 abstract description 10
- 238000007254 oxidation reaction Methods 0.000 abstract description 10
- 238000000576 coating method Methods 0.000 abstract description 9
- 239000011248 coating agent Substances 0.000 abstract description 8
- 239000007853 buffer solution Substances 0.000 abstract description 5
- 239000004088 foaming agent Substances 0.000 abstract description 3
- MUCZHBLJLSDCSD-UHFFFAOYSA-N diisopropyl fluorophosphate Chemical compound CC(C)OP(F)(=O)OC(C)C MUCZHBLJLSDCSD-UHFFFAOYSA-N 0.000 description 35
- 229960005051 fluostigmine Drugs 0.000 description 34
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical class Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 28
- 235000003351 Brassica cretica Nutrition 0.000 description 27
- 235000003343 Brassica rupestris Nutrition 0.000 description 27
- 235000010460 mustard Nutrition 0.000 description 27
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 26
- 241000219198 Brassica Species 0.000 description 23
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 20
- 238000012360 testing method Methods 0.000 description 14
- 231100000331 toxic Toxicity 0.000 description 12
- 230000002588 toxic effect Effects 0.000 description 12
- 239000002245 particle Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 239000013043 chemical agent Substances 0.000 description 10
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 10
- 230000005855 radiation Effects 0.000 description 10
- 239000000523 sample Substances 0.000 description 10
- 238000004458 analytical method Methods 0.000 description 9
- 238000013459 approach Methods 0.000 description 8
- 239000007844 bleaching agent Substances 0.000 description 8
- 238000011109 contamination Methods 0.000 description 7
- 230000006378 damage Effects 0.000 description 7
- 238000001514 detection method Methods 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000003973 paint Substances 0.000 description 7
- 239000004033 plastic Substances 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- 230000004044 response Effects 0.000 description 7
- 238000003860 storage Methods 0.000 description 7
- 241000193738 Bacillus anthracis Species 0.000 description 6
- JJIUCEJQJXNMHV-UHFFFAOYSA-N VX nerve agent Chemical compound CCOP(C)(=O)SCCN(C(C)C)C(C)C JJIUCEJQJXNMHV-UHFFFAOYSA-N 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000013618 particulate matter Substances 0.000 description 6
- 238000005086 pumping Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 238000001784 detoxification Methods 0.000 description 5
- 238000012544 monitoring process Methods 0.000 description 5
- 210000005036 nerve Anatomy 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 5
- 239000013535 sea water Substances 0.000 description 5
- 241000219193 Brassicaceae Species 0.000 description 4
- 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 4
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 4
- 230000003190 augmentative effect Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 231100000252 nontoxic Toxicity 0.000 description 4
- 230000003000 nontoxic effect Effects 0.000 description 4
- 230000002085 persistent effect Effects 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 238000005063 solubilization Methods 0.000 description 4
- 230000007928 solubilization Effects 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 230000003139 buffering effect Effects 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 231100001261 hazardous Toxicity 0.000 description 3
- 238000001819 mass spectrum Methods 0.000 description 3
- HAWPXGHAZFHHAD-UHFFFAOYSA-N mechlorethamine Chemical class ClCCN(C)CCCl HAWPXGHAZFHHAD-UHFFFAOYSA-N 0.000 description 3
- 229960004961 mechlorethamine Drugs 0.000 description 3
- 239000003958 nerve gas Substances 0.000 description 3
- 230000000269 nucleophilic effect Effects 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000005201 scrubbing Methods 0.000 description 3
- 230000003381 solubilizing effect Effects 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 230000001629 suppression Effects 0.000 description 3
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 2
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 208000033962 Fontaine progeroid syndrome Diseases 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 241000700605 Viruses Species 0.000 description 2
- 238000012387 aerosolization Methods 0.000 description 2
- 125000005233 alkylalcohol group Chemical group 0.000 description 2
- XUFUCDNVOXXQQC-UHFFFAOYSA-L azane;hydroxy-(hydroxy(dioxo)molybdenio)oxy-dioxomolybdenum Chemical compound N.N.O[Mo](=O)(=O)O[Mo](O)(=O)=O XUFUCDNVOXXQQC-UHFFFAOYSA-L 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
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- JGJLWPGRMCADHB-UHFFFAOYSA-N hypobromite Chemical compound Br[O-] JGJLWPGRMCADHB-UHFFFAOYSA-N 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
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- 159000000000 sodium salts Chemical class 0.000 description 2
- HQAITFAUVZBHNB-UHFFFAOYSA-N sodium;pentahydrate Chemical compound O.O.O.O.O.[Na] HQAITFAUVZBHNB-UHFFFAOYSA-N 0.000 description 2
- 238000010183 spectrum analysis Methods 0.000 description 2
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- 239000004711 α-olefin Substances 0.000 description 2
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 description 1
- UNWRHVZXVVTASG-UHFFFAOYSA-N 1,3-dichloro-1,3,5-triazinane-2,4,6-trione;sodium Chemical compound [Na].ClN1C(=O)NC(=O)N(Cl)C1=O UNWRHVZXVVTASG-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- IVTOWMZAZSBKOT-UHFFFAOYSA-N 3-[methoxy(methyl)phosphoryl]oxy-2,2-dimethylbutane Chemical compound COP(C)(=O)OC(C)C(C)(C)C IVTOWMZAZSBKOT-UHFFFAOYSA-N 0.000 description 1
- 102000012440 Acetylcholinesterase Human genes 0.000 description 1
- 108010022752 Acetylcholinesterase Proteins 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 102000006996 Aryldialkylphosphatase Human genes 0.000 description 1
- 108010008184 Aryldialkylphosphatase Proteins 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- MOMZHAUZKIBZHI-UHFFFAOYSA-N CC(C)N(CC[S+]=P(C)(O)O)C(C)C Chemical compound CC(C)N(CC[S+]=P(C)(O)O)C(C)C MOMZHAUZKIBZHI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- 206010010904 Convulsion Diseases 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
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- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- ICZWVCDXVPRBMM-UHFFFAOYSA-N OP(F)=O Chemical class OP(F)=O ICZWVCDXVPRBMM-UHFFFAOYSA-N 0.000 description 1
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- PJVJTCIRVMBVIA-JTQLQIEISA-N [dimethylamino(ethoxy)phosphoryl]formonitrile Chemical compound CCO[P@@](=O)(C#N)N(C)C PJVJTCIRVMBVIA-JTQLQIEISA-N 0.000 description 1
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- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
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- CODNYICXDISAEA-UHFFFAOYSA-N bromine monochloride Chemical compound BrCl CODNYICXDISAEA-UHFFFAOYSA-N 0.000 description 1
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- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 1
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- GSPKZYJPUDYKPI-UHFFFAOYSA-N diethoxy sulfate Chemical compound CCOOS(=O)(=O)OOCC GSPKZYJPUDYKPI-UHFFFAOYSA-N 0.000 description 1
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- 238000007865 diluting Methods 0.000 description 1
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- PXBBFIADSJLIFB-UHFFFAOYSA-O dimethyl-[(oxo-$l^{5}-phosphanylidyne)methyl]-(2-sulfanylethyl)azanium Chemical class SCC[N+](C)(C)C#P=O PXBBFIADSJLIFB-UHFFFAOYSA-O 0.000 description 1
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- 239000012530 fluid Substances 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 231100000518 lethal Toxicity 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- GIKLTQKNOXNBNY-OWOJBTEDSA-N lewisite Chemical compound Cl\C=C\[As](Cl)Cl GIKLTQKNOXNBNY-OWOJBTEDSA-N 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000013502 plastic waste Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000003247 radioactive fallout Substances 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000011012 sanitization Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940057950 sodium laureth sulfate Drugs 0.000 description 1
- PYILKOIEIHHYGD-UHFFFAOYSA-M sodium;1,5-dichloro-4,6-dioxo-1,3,5-triazin-2-olate;dihydrate Chemical compound O.O.[Na+].[O-]C1=NC(=O)N(Cl)C(=O)N1Cl PYILKOIEIHHYGD-UHFFFAOYSA-M 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- 231100000925 very toxic Toxicity 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
- A62D3/36—Detoxification by using acid or alkaline reagents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0094—High foaming compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- 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
-
- 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
- Y10S588/00—Hazardous or toxic waste destruction or containment
- Y10S588/901—Compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Emergency Management (AREA)
- Health & Medical Sciences (AREA)
- Business, Economics & Management (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12097199P | 1999-02-19 | 1999-02-19 | |
| PCT/CA2000/000137 WO2000048684A1 (en) | 1999-02-19 | 2000-02-15 | Broad spectrum decontamination formulation and method of use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL144978A0 IL144978A0 (en) | 2002-06-30 |
| IL144978A true IL144978A (en) | 2004-12-15 |
Family
ID=22393622
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL14497800A IL144978A (en) | 1999-02-19 | 2000-02-15 | Decontamination composition containing chloroisocyanuric acid, methods for the preparation thereof and kits containing the same |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6525237B1 (de) |
| EP (1) | EP1154820B1 (de) |
| AT (1) | ATE224756T1 (de) |
| AU (1) | AU769408B2 (de) |
| CA (1) | CA2300698C (de) |
| DE (1) | DE60000508T2 (de) |
| IL (1) | IL144978A (de) |
| WO (1) | WO2000048684A1 (de) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6723890B2 (en) | 1998-06-30 | 2004-04-20 | Sandia Corporation | Concentrated formulations and methods for neutralizing chemical and biological toxants |
| US7282470B2 (en) * | 2002-07-19 | 2007-10-16 | Sandia Corporation | Decontamination formulation with sorbent additive |
| US7390432B2 (en) | 1998-06-30 | 2008-06-24 | Sandia Corporation | Enhanced formulations for neutralization of chemical, biological and industrial toxants |
| SI1458386T1 (sl) | 2001-12-27 | 2007-08-31 | Ortho Mcneil Pharm Inc | Aroil pirol heteroeril in metanoli, uporabni za zdravljenje motnje centralnega živčnega sistema |
| US7384183B2 (en) * | 2002-09-06 | 2008-06-10 | Global Ground Support, Llc | Mobile decontamination unit |
| AU2003297808A1 (en) | 2002-12-09 | 2004-06-30 | The Trustees Of Columbia University In The City Of New York | Peptides and methods for deactivation of organophosphorus-based nerve agents and insecticides |
| WO2004080543A2 (en) | 2003-03-12 | 2004-09-23 | Queen's University At Kingston | Method of decomposing organophosphorus compounds |
| RU2248234C2 (ru) * | 2003-04-08 | 2005-03-20 | Федеральное государственное унитарное предприятие "Государственный научно-исследовательский институт биологического приборостроения" (ФГУП "ГосНИИ БП") | Бифункциональная рецептура окислительно-нуклеофильного действия |
| WO2006076406A2 (en) * | 2005-01-11 | 2006-07-20 | Clean Earth Technologies, Llc | Formulations for the decontamination of toxic chemicals |
| CA2593822C (en) * | 2005-01-11 | 2012-08-07 | Clean Earth Technologies, Llc | Peracid/ peroxide composition and use thereof as an anti-microbial and a photosensitizer |
| CN102006910A (zh) * | 2005-06-03 | 2011-04-06 | 美国全球豪微空间公司 | 生物净化系统 |
| EP1926682A4 (de) * | 2005-06-21 | 2012-06-20 | Crosslink Polymer Res | Signalaktivierte dekontaminierungsbeschichtung |
| US7846888B2 (en) * | 2006-02-07 | 2010-12-07 | Battelle Energy Alliance, Llc | Long lasting decontamination foam |
| WO2007098555A1 (en) * | 2006-03-03 | 2007-09-07 | Anadis Ltd | Method and apparatus for containment and decontamination |
| US7718594B1 (en) | 2006-10-11 | 2010-05-18 | The United States Of America As Represented By The Secretary Of The Navy | Aqueous based chemical and biological warfare decontaminating system for extreme temperature applications |
| WO2008053440A1 (en) * | 2006-10-31 | 2008-05-08 | The Procter & Gamble Company | Portable bio-chemical decontaminant system and method of using the same |
| US20090187060A1 (en) | 2008-01-22 | 2009-07-23 | E-Z-Em, Inc. | Method and Formulation for Neutralizing Toxic Chemicals and Materials |
| US20100179368A1 (en) * | 2008-11-07 | 2010-07-15 | Aries Associates, Inc. | Novel Chemistries, Solutions, and Dispersal Systems for Decontamination of Chemical and Biological Systems |
| US20100119412A1 (en) * | 2008-11-07 | 2010-05-13 | Aries Associates, Inc. | Novel Chemistries, Solutions, and Dispersal Systems for Decontamination of Chemical and Biological Systems |
| DE102009002681A1 (de) | 2009-02-18 | 2010-09-09 | Areva Np Gmbh | Verfahren zur Dekontamination radioaktiv kontaminierter Oberflächen |
| US8518941B2 (en) * | 2010-08-19 | 2013-08-27 | American Sterilizer Company | Extreme temperature aqueous decontamination composition |
| CA2783349A1 (en) * | 2012-07-18 | 2014-01-18 | Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of Environment | Decontamination of radionuclides on construction materials |
| US9499772B2 (en) | 2013-03-13 | 2016-11-22 | Battelle Energy Alliance, Llc | Methods of decontaminating surfaces and related compositions |
| CN106999618A (zh) | 2014-12-08 | 2017-08-01 | 金诺斯公司 | 用于颜料消毒的添加剂组合物及其方法 |
| EP3414311A4 (de) | 2016-02-12 | 2019-09-04 | Kinnos Inc. | Zusammensetzungen und verfahren zur verwendung bei der oberflächendekontamination |
| EP3487974A4 (de) | 2016-07-25 | 2020-08-05 | Kinnos Inc. | Vorrichtung und zugehörige zusammensetzungen und verfahren zur verwendung bei der oberflächendekontamination |
| CN109069894B (zh) * | 2017-03-03 | 2021-07-06 | 美国傲世环保科技公司 | 使用共聚物与凝聚聚合物系统的组合原位微包封处理石棉纤维和其它有害材料 |
| US11464371B2 (en) | 2018-07-12 | 2022-10-11 | Kinnos Inc. | Devices, compositions, and methods for use in surface decontamination |
| MX2021004968A (es) * | 2018-10-29 | 2021-06-15 | Dow Global Technologies Llc | Deshidratacion de gas. |
| US10369396B1 (en) | 2018-11-09 | 2019-08-06 | Battelle Memorial Institute | Assembly for decontaminating and method of manufacturing the assembly |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5271592A (en) * | 1975-12-12 | 1977-06-15 | Mitsubishi Chem Ind Ltd | Production of regenerared nylon resin |
| ZA775615B (en) | 1976-10-26 | 1978-08-30 | Stauffer Chemical Co | Hard surface cleaning composition |
| JPS5953314B2 (ja) * | 1980-04-09 | 1984-12-24 | 花王株式会社 | 発泡性組成物 |
| JPS56143300A (en) * | 1980-04-09 | 1981-11-07 | Kao Corp | Foamable composition |
| DE3036153C2 (de) * | 1980-09-23 | 1985-06-27 | Herbert Lindner Gmbh, 1000 Berlin | Vorrichtung zum Hinterschleifen und Polygonschleifen an Schleifmaschinen |
| EP0051687B1 (de) * | 1980-11-07 | 1984-05-16 | MITSUI TOATSU CHEMICALS, Inc. | Maleinimide und Verfahren zu ihrer Herstellung |
| US4543872A (en) | 1983-08-08 | 1985-10-01 | Graham Kenneth J | Blast attenuator |
| US4589341A (en) | 1984-02-10 | 1986-05-20 | Rockwood Systems Corporation | Method for explosive blast control using expanded foam |
| US4744917A (en) | 1985-07-31 | 1988-05-17 | Olin Corporation | Toxic chemical agent decontamination emulsions, their preparation and application |
| US4908215A (en) | 1986-03-06 | 1990-03-13 | Brandeis University | Hypochlorite compositions containing thiosulfate and use thereof |
| KR930009035B1 (ko) * | 1990-03-19 | 1993-09-22 | 국방과학연구소 | 수용성 제독제 조성물 |
| FR2679458A1 (fr) * | 1991-07-23 | 1993-01-29 | Commissariat Energie Atomique | Mousse de decontamination a duree de vie controlee et installation de decontamination d'objets utilisant une telle mousse. |
| KR940006580B1 (ko) | 1991-10-15 | 1994-07-22 | 금성익렉트론 주식회사 | 접착리드를 이용한 반도체 패키지 구조 및 그 제조방법 |
| DE19526380A1 (de) * | 1995-07-19 | 1997-01-23 | Henkel Ecolab Gmbh & Co Ohg | Pastöses Geschirreinigungsmittel und seine Herstellung |
| US5723095A (en) | 1995-12-28 | 1998-03-03 | Steris Corporation | Cleaner concentrate formulation for biological waste fluid handling systems |
| 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 |
| US5859064A (en) | 1996-03-13 | 1999-01-12 | The United States Of America As Represented By The Secretary Of The Navy | Chemical warfare agent decontamination solution |
| AU6646798A (en) | 1997-01-10 | 1998-08-03 | Loizeaux Group Int'l Ltd | Method and apparatus for the destruction of articles |
| US5864767A (en) | 1997-06-09 | 1999-01-26 | The United States Of America As Represented By The Secretary Of The Army | Chemical biological explosive containment system |
| JP3983353B2 (ja) * | 1997-11-14 | 2007-09-26 | 花王株式会社 | 硬質体用の固形殺菌洗浄剤 |
| US6405626B1 (en) * | 1999-02-26 | 2002-06-18 | Her Majesty The Queen In Right Of Canada As Represented By The Solicitor General Acting Through The Commissioner Of The Royal Canadian Mounted Police | Decontaminating and dispersion suppressing foam formulation |
-
2000
- 2000-02-14 CA CA002300698A patent/CA2300698C/en not_active Expired - Fee Related
- 2000-02-15 DE DE60000508T patent/DE60000508T2/de not_active Expired - Lifetime
- 2000-02-15 AT AT00903467T patent/ATE224756T1/de active
- 2000-02-15 WO PCT/CA2000/000137 patent/WO2000048684A1/en not_active Ceased
- 2000-02-15 EP EP00903467A patent/EP1154820B1/de not_active Expired - Lifetime
- 2000-02-15 AU AU25302/00A patent/AU769408B2/en not_active Ceased
- 2000-02-15 IL IL14497800A patent/IL144978A/en not_active IP Right Cessation
- 2000-02-16 US US09/504,932 patent/US6525237B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ATE224756T1 (de) | 2002-10-15 |
| IL144978A0 (en) | 2002-06-30 |
| US6525237B1 (en) | 2003-02-25 |
| WO2000048684A1 (en) | 2000-08-24 |
| EP1154820B1 (de) | 2002-09-25 |
| CA2300698A1 (en) | 2000-08-19 |
| DE60000508D1 (de) | 2002-10-31 |
| AU2530200A (en) | 2000-09-04 |
| CA2300698C (en) | 2003-10-07 |
| EP1154820A1 (de) | 2001-11-21 |
| AU769408B2 (en) | 2004-01-29 |
| DE60000508T2 (de) | 2003-01-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| KB | Patent renewed | ||
| KB | Patent renewed | ||
| MM9K | Patent not in force due to non-payment of renewal fees |