WO2006135620A1 - Vapor phase hydrogen peroxide deodorizer - Google Patents
Vapor phase hydrogen peroxide deodorizer Download PDFInfo
- Publication number
- WO2006135620A1 WO2006135620A1 PCT/US2006/022027 US2006022027W WO2006135620A1 WO 2006135620 A1 WO2006135620 A1 WO 2006135620A1 US 2006022027 W US2006022027 W US 2006022027W WO 2006135620 A1 WO2006135620 A1 WO 2006135620A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hydrogen peroxide
- solid
- vapor phase
- peroxohydrate
- compositions
- Prior art date
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 title claims abstract description 276
- 239000012808 vapor phase Substances 0.000 title claims abstract description 56
- 239000000203 mixture Substances 0.000 claims abstract description 88
- 238000000034 method Methods 0.000 claims abstract description 41
- 239000007787 solid Substances 0.000 claims abstract description 39
- 239000007788 liquid Substances 0.000 claims abstract description 35
- 239000008247 solid mixture Substances 0.000 claims abstract description 27
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- 230000002378 acidificating effect Effects 0.000 claims abstract description 22
- 230000007935 neutral effect Effects 0.000 claims abstract description 17
- 230000008020 evaporation Effects 0.000 claims abstract description 13
- 238000001704 evaporation Methods 0.000 claims abstract description 13
- 239000003205 fragrance Substances 0.000 claims description 10
- 239000003381 stabilizer Substances 0.000 claims description 8
- 238000000859 sublimation Methods 0.000 claims description 7
- 230000008022 sublimation Effects 0.000 claims description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 6
- 235000011152 sodium sulphate Nutrition 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000003086 colorant Substances 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- 239000007891 compressed tablet Substances 0.000 claims description 3
- 238000010979 pH adjustment Methods 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 claims description 2
- 239000008187 granular material Substances 0.000 claims description 2
- 238000012545 processing Methods 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 239000003349 gelling agent Substances 0.000 claims 2
- 230000009467 reduction Effects 0.000 abstract description 26
- 238000003379 elimination reaction Methods 0.000 abstract description 19
- 230000008030 elimination Effects 0.000 abstract description 18
- 229960002163 hydrogen peroxide Drugs 0.000 description 121
- 239000003570 air Substances 0.000 description 39
- 239000000779 smoke Substances 0.000 description 27
- 235000019645 odor Nutrition 0.000 description 22
- 239000004744 fabric Substances 0.000 description 19
- 239000000126 substance Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000007789 gas Substances 0.000 description 14
- 238000011282 treatment Methods 0.000 description 13
- 241000208125 Nicotiana Species 0.000 description 11
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 230000008569 process Effects 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 9
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 8
- 150000002978 peroxides Chemical class 0.000 description 8
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 5
- -1 transition metal salt Chemical class 0.000 description 5
- 239000004155 Chlorine dioxide Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000012080 ambient air Substances 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 4
- 235000019398 chlorine dioxide Nutrition 0.000 description 4
- 230000001877 deodorizing effect Effects 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 4
- 239000010865 sewage Substances 0.000 description 4
- 229940045872 sodium percarbonate Drugs 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000019504 cigarettes Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000005201 scrubbing Methods 0.000 description 3
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene 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
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000004775 Tyvek Substances 0.000 description 2
- 229920000690 Tyvek Polymers 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000013068 control sample Substances 0.000 description 2
- 238000010411 cooking Methods 0.000 description 2
- 239000002781 deodorant agent Substances 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- 238000007323 disproportionation reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- GBHRVZIGDIUCJB-UHFFFAOYSA-N hydrogenphosphite Chemical class OP([O-])[O-] GBHRVZIGDIUCJB-UHFFFAOYSA-N 0.000 description 2
- 229940006477 nitrate ion Drugs 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000002470 solid-phase micro-extraction Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 125000005402 stannate group Chemical group 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 230000002110 toxicologic effect Effects 0.000 description 2
- 231100000027 toxicology Toxicity 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000002386 air freshener Substances 0.000 description 1
- 239000000809 air pollutant Substances 0.000 description 1
- 231100001243 air pollutant Toxicity 0.000 description 1
- 229910052936 alkali metal sulfate Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000011208 chromatographic data Methods 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000007771 core particle Substances 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004924 electrostatic deposition Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229910001448 ferrous ion Inorganic materials 0.000 description 1
- 239000003897 fog Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 239000010808 liquid waste Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 230000008447 perception Effects 0.000 description 1
- 231100000754 permissible exposure limit Toxicity 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000019505 tobacco product Nutrition 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
Definitions
- This invention relates to odor reduction or elimination from air spaces and surfaces through the generation and use of vapor phase hydrogen peroxide. Specifically, the invention relates to compositions and methods by which odor reduction or elimination is accomplished using vapor phase hydrogen peroxide. More specifically, the invention relates to methods by which odors such as smoke are reduced or eliminated by the generation of vapor phase hydrogen peroxide from pH neutral to mildly acidic aqueous compositions or solid compositions containing at least one pH neutral to mildly acidic hydrogen peroxide containing compound.
- Malodorous substances can be present in or on a variety of media or surfaces. Individuals can be highly aware of malodors on indoor surfaces and contained in indoor air, since there is generally limited air exchange and circulation in the indoor environment in comparison to the outdoor environment. Furthermore, olfactory detection of certain malodors in many indoor settings, such as residential homes, hotels, automobile interiors, hospitals, and office buildings may give rise to a perception that the indoor area is unsanitary or soiled. Other odors, such as those originating from certain foods, cooking activities, and burned tobacco products, while not generally thought of as unsanitary or dirty, can be regarded as unpleasant by many people. Thus, there exists a need for effective removal of malodors which reside on indoor surfaces or are contained within the indoor air space.
- U.S. Patent No. 4,036,994 discloses the use of aqueous hydrogen peroxide solutions to remove cooked food and smoke odors from the restaurant broiling grill emissions, in part through scrubbing of the grill exhaust gas stream with these solutions.
- the malodor elimination process described in this patent requires cooking foods over thin, high temperature ceramic briquets to enhance incineration of potential malodors, as well as scrubbing the grill exhaust gas stream with an aqueous hydrogen peroxide solution, followed by mixing the treated gas with ambient air prior to discharge to the atmosphere.
- U.S. Patent No. 5,904,901 discloses removal of odors from indoor environments using an apparatus which generates and discharges both ozone and an atomized hydrogen peroxide solution, whereby reaction between ozone and atomized hydrogen peroxide generates hydroxyl radical and is said to decompose various malodorous substances present in the indoor environment .
- U.S. Patent Nos. 5,071,622 and 5,137,687 disclose processes by which malodorous substances are removed from sewage treatment systems that emit odors.
- odor abatement is obtained by contacting hydrophobic components of an odor-containing gas plume condensate with odor-trapping core particles containing precipitates resulting from reaction of ferrous ion, tannic acid, and hydrogen peroxide .
- U.S. Patent Nos. 6,365,099 Bl and 6,495,096 Bl disclose processes and systems by which malodorous reduced sulfur compounds are removed from liquid waste streams associated with sewage collection/treatment.
- the '096 patent describes a treatment process which utilizes aqueous deodorant compositions containing hydrogen peroxide and nitrate ion or hydrogen peroxide, nitrate ion, and a transition metal salt.
- the aqueous deodorant compositions of the '096 patent are mixed directly with the waste stream.
- U.S. Patent No. 6,815,408 B2 discloses aqueous alkaline phosphate-containing hydrogen peroxide compositions for various odor elimination and disinfection uses. The aqueous compositions are introduced onto surfaces and into air handling ducts by the application of a spray or mist of the aqueous alkaline peroxide solutions.
- WO 94/11091 discloses a catalytic process for removal of odors from industrial gas streams by scrubbing such gas streams through a fixed bed scrubber fitted with a solid packing bed containing a transition metal catalyst and a hydrogen peroxide-containing liquor.
- ozone gas is known to effectively react with and eliminate many types of malodors .
- ozone may be regarded as a hazardous indoor air pollutant, and exposure to ozone in indoor air is strictly regulated by the U.S. Environmental Protection Agency ("EPA") for many indoor environments.
- EPA U.S. Environmental Protection Agency
- chlorine dioxide gas can be employed as a reactive malodor- eliminating reagent.
- exposure to chlorine dioxide is of significant toxicological concern and the EPA has established very low permissible exposure limits to this substance.
- chlorine dioxide has a very low human odor detection threshold and many individuals tend to find the odor of chlorine dioxide objectionable well below the established EPA airborne exposure limits.
- the present invention provides for compositions and methods of reducing or eliminating malodors from indoor air and from surfaces located within indoor environments.
- the invention has been found to be particularly useful in reducing or eliminating cigarette odors from such environments .
- a method of the invention provides for the elimination or reduction of malodors from air and surfaces within an indoor environment by the use of vapor phase hydrogen peroxide which is generated by the passive evaporation of pH neutral to mildly acidic aqueous-based liquid compositions.
- the aqueous-based liquid compositions contain no more than about 8% hydrogen peroxide by weight.
- Passive evaporation means that vapor phase hydrogen peroxide is slowly generated over an extended period of time by evaporation directly from a bulk aqueous composition.
- the pH range of the liquid hydrogen peroxide composition is preferably in the range of about pH 8 to about pH 1 in the temperature range of about 15-30 0 C.
- the pH neutral to mildly acidic aqueous-based liquid compositions may comprise low viscosity fluids, viscous gels, or thick suspensions, and may also include other ingredients including fragrance/perfume ingredients.
- Another method of the present invention provides for the elimination or reduction of malodors from air and surfaces within an indoor environment using vapor phase hydrogen peroxide generated by sublimation of hydrogen peroxide from a solid composition containing at least one pH neutral to mildly acidic solid hydrogen peroxide-containing peroxohydrate compound.
- sublimation refers to a process by which hydrogen peroxide vapor is directly released from the hydrogen peroxide-containing solid.
- pH neutral to slightly acidic hydrogen peroxide-containing peroxohydrate compound refers to a compound containing molecular hydrogen peroxide wherein the pH of a concentrated solution of the compound in purified water is less than about pH 8 in the temperature range of about 20-25 0 C.
- suitable mildly acidic hydrogen peroxide-containing peroxohydrate compounds include urea peroxohydrate, CO (NH 2 ) 2 'H 2 O 2 ; sodium sulfate peroxohydrate, 2Na 2 SO 4 'H 2 O 2 '2H 2 O; and a peroxohydrate of poly (vinyl pyrrolidone) polymer, PVP-XH 2 O 2 .
- the solid composition containing one or more peroxide-containing compounds may also include one or more non-peroxide containing solids, such as inert inorganic salts or solid organic compound fillers.
- the solid may comprise a powder, compressed tablet, crystalline solid, or other readily recognizable solid forms.
- the solid compositions may also include minor amounts of liquid or solid fragrance/perfume ingredients.
- Hydrogen peroxide in its pure form is a clear, colorless liquid having a slightly sharp acrid odor and a freezing point of -0.4 0 C.
- Pure liquid hydrogen peroxide exhibits a vapor pressure of ca. 2.0 mm Hg at 25°C, somewhat less than that of water (ca. 24 mm Hg at 25°C) .
- Aqueous solutions of hydrogen peroxide exhibit a mixed vapor phase composition of water vapor and vapor phase hydrogen peroxide, as expected for a mixture of two miscible volatile liquids. See, for example, "Hydrogen Peroxide" in Kirk-Othmer Encyclopedia of Chemical Technology, 4 th Edition, Volume 13, 1995, Wiley-Interscience Publication, and references therein.
- peroxohydrates or perhydrates Inorganic and organic compounds containing molecular hydrogen peroxide as solid/crystalline adducts are referred to as peroxohydrates or perhydrates .
- Many such materials are known in the commercial and technical literature, including such materials as sodium carbonate peroxohydrate 2Na 2 CO 3 -BH 2 O 2 (sodium percarbonate) ; ammonium carbonate peroxohydrate, (NH 4 ) 2CO 3 -H 2 O 2 ; urea peroxohydrate, CO (NH 2 ) 2 'H 2 O 2 (urea peroxide); sodium sulfate peroxohydrate, 2Na 2 SO 4 'H 2 O 2 '2H 2 O; and various peroxohydrate phosphate salts.
- aqueous liquid compositions containing hydrogen peroxide wherein the pH of the solution is about 8 or below, can be passively evaporated in an indoor environment to produce useful amounts of vapor phase hydrogen peroxide with utility toward the elimination or reduction of malodors from the air space and surfaces of the indoor environment.
- Alkaline aqueous hydrogen peroxide solutions are not stable with respect to disproportionation to water and oxygen gas. Therefore, it is desirable to utilize pH neutral to mildly acidic aqueous hydrogen peroxide compositions in the pH range of about 1 to about 8. This provides acceptable long-term stability of the aqueous hydrogen peroxide composition. More preferably, the pH of the liquid composition is in the range of about 2 to about 7.
- the pH of the liquid composition is in the range of about 3 to about 6, providing for optimal product stability.
- the method of the present invention is directed to the passive evaporation of the hydrogen peroxide into the indoor air space.
- Passive evaporation means that vapor phase hydrogen peroxide is slowly generated over an extended period of time by evaporation directly from a bulk aqueous composition. This excludes processes whereby the aqueous compositions are dispersed into the indoor air, or applied directly to indoor surfaces as bulk liquid or as liquid droplets using mechanical means such as pouring, spraying, misting, fogging, or atomizing via manually operated or powered devices .
- the aqueous pH neutral to mildly acidic aqueous hydrogen peroxide compositions may be homogeneous solutions or heterogeneous dispersions containing suspended solids.
- the viscosity of the liquid hydrogen peroxide compositions may range from that of a "water-thin" fluid (less than about 10 centipoise at 25°C) to that of a highly viscous, rigid gel, paste or suspension (about 100,000 cps or greater at 25 0 C) .
- Viscosity building agents may include peroxide-stable surfactant systems, peroxide-stable polymers, as well as various solid inorganic thickening agents/fillers such as alumina, silica, and natural/synthetic clays .
- the concentration of hydrogen peroxide in the aqueous compositions may comprise up to about 50% by weight of the composition, preferably less than about 10% by weight of the composition and most preferably about 8% to about 0.5% by weight of the composition.
- the aqueous compositions may include minor amounts of other ingredients, including fragrance ingredients and fragrance solubilizing agents such as surfactants or solvents, and/or colorant (s) for aesthetic purposes.
- the aqueous compositions may also include one or more hydrogen peroxide-stabilizing agents, such as, for example, stannate compounds, phosphate salts, organophosphonates, and various chelating agents derived from aminocarboxylates or aminophosphonates .
- stannate compounds such as, for example, stannate compounds, phosphate salts, organophosphonates, and various chelating agents derived from aminocarboxylates or aminophosphonates.
- Various peroxide-stabilizing agents are disclosed in "Hydrogen Peroxide, Stabilization", Kirk
- Additional ingredients may include peroxide-stable acids for pH adjustment, including but not limited, to sulfuric acid, phosphoric acid, sulfamic acid, acetic acid, propanoic acid, citric acid, adipic acid, glutaric acid, succinic acid, and polyacrylic acid.
- peroxide-stable acids for pH adjustment, including but not limited, to sulfuric acid, phosphoric acid, sulfamic acid, acetic acid, propanoic acid, citric acid, adipic acid, glutaric acid, succinic acid, and polyacrylic acid.
- Various dispensing devices are suitable for malodor reduction or elimination applications using passive generation of vapor phase hydrogen peroxide from low viscosity aqueous hydrogen peroxide-containing solutions. Liquid wicking devices, such as container-dispensing systems for liquid air fresheners, are especially useful.
- Container- dispensing devices suitable for the methods and compositions of the present invention disclosed herein include those set forth in U.S. Patent Nos . 2,802,695; 3,550,853; 4,286,754; 4,413,779; 4,913,350; 5,000,383; 5,014,913; 5,121,881; 5,749,519; 5,749,520; 5,875,968 and 6,871,794 B2 , incorporated herein by reference. Materials of construction for such devices are selected so as to provide for the integrity of the container-dispenser with respect to the oxidizing and corrosive nature of the aqueous hydrogen peroxide solutions described in the present invention.
- Viscous gels or suspensions of the present invention may be contained within dish or cup type containers, having at least one opening so as to permit the passive evaporation of the hydrogen peroxide-containing composition, producing a suitable concentration of vapor phase hydrogen peroxide in the indoor air space.
- suitable containers include those disclosed in U.S. Design Patent Nos . 295,675; 307,469; 332,999; and 376,002, incorporated herein by reference.
- Various mechanical devices may be utilized in combination with hydrogen peroxide-containing viscous gels or suspensions of the present invention. These devices include those which will enhance effective generation of vapor phase hydrogen peroxide within the indoor environments by utilizing mild heating of the inventive compositions, which are enclosed within appropriate containers. Such heating devices, used to promote the dispensing of volatile liquid compositions, include those disclosed in U.S. Patent Nos. 3,633,881; 4,020,321; 4,968,487; 5,038,394; 5,290,546;
- Fan type devices may also be employed to enhance the generation of vapor phase hydrogen peroxide within the indoor environments by flowing a stream of air across the inventive compositions, which are enclosed within appropriate containers .
- Such fan type devices, used to promote the dispensing of volatile liquid compositions include those disclosed in U.S. Patent Nos. 4,840,770; 5,370,829; 5,547,616; 6,361,752 Bl and 6,371,450 Bl, incorporated herein by reference.
- peroxohydrate compounds when exposed to ambient indoor air, will liberate useful amounts of vapor phase hydrogen peroxide with utility towards reduction or elimination of malodors from the air space and surfaces of the indoor environment .
- These peroxohydrate compounds may comprise part, or all, of solid compositions which sublime hydrogen peroxide from the solid composition into the vapor phase at ambient room temperatures.
- the amount of peroxohydrate utilized in the solid composition will depend on the hydrogen peroxide content of the peroxohydrate and the release rate of hydrogen peroxide vapor from a given peroxohydrate, relative to the desired rate of release for the composition containing the peroxohydrate.
- pH neutral to slightly acidic peroxohydrate compound refers to a peroxohydrate compound wherein the pH of a concentrated (ca. 5% by weight in water) solution of the compound in purified water is less than about pH 8 in the temperature range of about 20-25 0 C.
- suitable mildly acidic hydrogen peroxide-containing peroxohydrate compounds include urea peroxohydrate, CO (NH 2 ) 2 'H 2 O 2 ; sodium sulfate peroxohydrate, 2Na 2 SO 4 'H 2 O 2 '2H 2 O, and a peroxohydrate of poly (vinyl pyrrolidone) polymer, PVP-H 2 O 2 , where the hydrogen peroxide content of the polymeric PVP peroxohydrate can range up to about 22 % by weight.
- the solid composition containing one or more peroxide-containing peroxohydrate compounds may also include one or more non-peroxide containing filler solids, such as inert inorganic salts or solid organic compounds.
- the solid composition may comprise a powder, compressed tablet, crystalline solid, or other readily recognizable solid forms.
- the hydrogen peroxide content of the solid composition can be as high as about 50% by weight hydrogen peroxide, but preferably about 25% by weight or less for reasons of, among other things, product processing and stability. More preferably, the solid compositions have a hydrogen peroxide content in the range of about 0.1% to about 10% by weight. Most preferably, the solid compositions have a hydrogen peroxide content in the range of about 0.5% to about 8% by weight.
- the solid composition may include minor amounts of other ingredients, including fragrance ingredients, and/or colorant (s) for aesthetic purposes. Minor amount of other ingredients, such as surfactants, solvents, and processing aids (e.g., anticaking agents, mold release agents, shape- forming agents or binders, etc.) may also be included in the solid compositions of the present invention.
- the compositions of the present invention may also include one or more hydrogen peroxide-stabilizing agents, such as stannate compounds, phosphate salts, organophosphonates, and various chelating agents derived from aminocarboxylates or aminophosphonates .
- the solid hydrogen-peroxide-containing compositions of this invention may be packaged within various types of containers which permit the sublimation of vapor phase hydrogen peroxide into the indoor air space. These packages include pouches or bags, which allow for the transmission of hydrogen peroxide vapor through the package walls.
- the solid compositions may also be contained within a cup or dish having one or more suitable openings which permit vapor phase hydrogen peroxide transmission from within the container into the indoor air space.
- a container such as a dish or cup may include a physical barrier preventing the solid from being discharged from the container by shaking, inverting, or the like.
- Appropriate physical barriers include a covering of fabric or screen-type material of sufficiently small pore/mesh size, such that the solid powder or particulate can not pass though the fabric/screen, however the pores in the covering will allow for the transmission of vapor phase hydrogen peroxide into the indoor air space .
- Various mechanical devices may be utilized in combination with hydrogen peroxide-containing solid compositions of the present invention.
- These devices include those which will enhance effective generation of vapor phase hydrogen peroxide within the indoor environments by utilizing mild heating of the inventive compositions, which are enclosed within appropriate containers.
- Such heating devices, used to promote the dispensing of volatile compositions include those disclosed in U.S. Patent Nos . 3,633,881; 4,020,321; 4,968,487; 5,038,394; 5,290,546; 5,647,053; 5,903,710; 5,945,094; 5,976,503; 6,123,935; and 6,862,403 B2, incorporated herein by reference.
- Fan type devices may also be employed to enhance the generation of vapor phase hydrogen peroxide within the indoor environments by flowing a stream of air across the inventive compositions, which are enclosed within appropriate containers.
- Such fan type devices, used to promote the dispensing of volatile compositions include those disclosed in U.S. Patent Nos. 4,840,770; 5,370,829;
- Solid compositions of the present invention may also be employed in the form of a powder or other solid particulate, to be purposefully dispensed for example, by shaking, from a container for application to household surfaces such as carpet or upholstery.
- Solid hydrogen peroxide-containing compositions of this invention may also be molded into single-piece articles including a tablet, disk, puck, cube, ball, or other appropriate shape.
- the matrix and surface area of the solid article are designed to allow for effective transmission of hydrogen peroxide through the bulk composition with sublimation of hydrogen peroxide vapor from the surface of the article.
- compositions and methods to be useful for the reduction or elimination of tobacco smoke odors from textiles, fabrics (such as clothing, furniture coverings, carpets, window treatments, etc.), and other indoor surfaces, and for the reduction or elimination of various other malodors, especially those containing reduced sulfur and nitrogen compounds, from both the air space and various surfaces within indoor environments.
- fabrics such as clothing, furniture coverings, carpets, window treatments, etc.
- various other malodors especially those containing reduced sulfur and nitrogen compounds
- Example 1 Vapor Phase Hydrogen Peroxide Generation From Aqueous Liquid Hydrogen Peroxide Compositions
- Three 50 gram samples of liquid aqueous hydrogen peroxide compositions as set forth in Table 1 were placed in individual 66 liter polypropylene test chambers, maintained at 23 'C. Vapor phase hydrogen peroxide concentrations inside the test chambers were quantified over extended periods of time using a Draeger Pac III ® gas monitor, fitted with a hydrogen peroxide sensor from Draeger Safety, Inc., Pittsburgh, PA, USA. The vapor phase hydrogen peroxide generation is expressed in units of ppm and is set forth in Table 2. [00037] Table 1: Aqueous Acidic Hydrogen Peroxide Compositions 1, 2, 3
- Dequest 2010 1-hydroxyethylidene-l, 1-phosphonic acid, 60% active in water. Solutia, Inc., St. Louis, MO, USA.
- Table 2 Vapor Phase Hydrogen Peroxide Generation From Aqueous Liquid Hydrogen Peroxide Compositions Of Table 1
- Example 2 Vapor Phase Hydrogen Peroxide Generation From Solid Hydrogen Peroxide Compositions
- Samples of solid peroxohydrate or perborate compositions, compositions 4-7 as set forth in Table 3, were placed in individual 66 liter polypropylene test chambers, maintained at 23 0 C, and 20% or 80% relative humidity. The pH values of these compositions are set forth in Table 4. Vapor phase hydrogen peroxide concentrations inside the test chambers were quantified over extended periods of time using a Draeger Pac III ® gas monitor, fitted with a hydrogen peroxide sensor from Draeger Safety, Inc., Pittsburgh, PA, USA. Vapor phase hydrogen peroxide generation is expressed in units of ppm and is set forth in Tables 5 and 6. [00041] Table 3: Composition 4 10 grams sodium perborate monohydrate compound in open petri dish.
- Composition 5 10 grams sodium percarbonate compound in open petri dish.
- Composition 6 7.2 grams Peroxydone ® polyvinylpyrrolidone- hydrogen peroxide complex (22 % hydrogen peroxide content) , 12.8 grams sodium sulfate, combined solids contained within TYVEK ® pouch from DuPont Company, Wilmington, Delaware, USA.
- Composition 7 4.8 grams urea-hydrogen peroxide complex (33 % hydrogen peroxide content), 15.2 grams sodium sulfate, combined solids contained within TYVEK ® pouch from DuPont Company, Wilmington, Delaware, USA.
- Example 3 Reduction Of Tobacco Smoke Malodors From Fabric Using Vapor Phase Hydrogen Peroxide, Generated Via Passive Evaporation Of An Aqueous Liquid Composition Containing Hydrogen Peroxide ,
- vapor phase hydrogen peroxide was generated from the passive evaporation of an 8% aqueous solution of hydrogen peroxide in water, identical to composition 1 (Table 1) . 50 grams of 8% aqueous solution was evenly divided between two petri dishes, which were then placed on the floor of the chamber. The concentration of vapor phase hydrogen peroxide in the room was allowed to reach equilibrium (within 24 hours) and was measured as 1.3- 1.5 ppm using a Draeger Pac III ® gas monitor, fitted with a hydrogen peroxide sensor.
- Example 4 Analytical Measurement Of Tobacco Smoke Malodor Component Reduction From Smoke-Treated Fabric Using Vapor Phase Hydrogen Peroxide
- Treatment of tobacco smoke impregnated cotton fabric with vapor phase hydrogen peroxide involved placing a 20 gram pouch of Composition 6 (Example 2) , 1 gram of water on a paper blotter, and the smoke-treated fabric into a 1 gallon glass jar.
- a similar control sample consisted of the smoke treated fabric plus the water/blotter in a 1-gallon glass jar with ambient room air. The fabric was suspended from the lid of the jar. Static headspace samples were collected after 24 and 48 hours using solid phase microextraction (SPME, Supleco part #57326-U, Stableflex 65 ⁇ m thick film, PDMS-DVB) .
- Table 8 Smoke Treated Cloth Exposed To Vapor Phase Hydrogen Peroxide Compared To Control Cloth. Percent Peak Area Reduction For Tobacco Smoke Gas Phase Components, 24 And 48 Hours Exposure Times
- Example 3 The "sniff test panel" results in Example 3 and the analytical results from Example 4 demonstrate the correlation between the perceived (olefactory) reduction in smoke malodor and the analytical quantification of malodor component reduction using compositions and methods of this invention.
- Alternative embodiments of the invention employing pH neutral to mildly acidic liquid hydrogen peroxide compositions may also be effective for application towards the reduction or elimination of malodors from indoor air and indoor surfaces.
- Such embodiments may include the physical dispersal of aqueous liquid into the indoor airspace as droplet, mist, or aerosol form. Additional embodiments may include spraying, misting, or pouring such aqueous compositions onto indoor surfaces. These embodiments may be accomplished by a variety of means, including using manual (user actuated) devices such as a hand operated trigger/pump sprayer or a pressurized aerosol can, or through the use of an electrically powered spraying device.
Landscapes
- Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06772367A EP1901785A1 (en) | 2005-06-10 | 2006-06-07 | Vapor phase hydrogen peroxide deodorizer |
JP2008515849A JP2008543369A (en) | 2005-06-10 | 2006-06-07 | Vapor phase hydrogen peroxide deodorant |
AU2006258117A AU2006258117B2 (en) | 2005-06-10 | 2006-06-07 | Vapor phase hydrogen peroxide deodorizer |
CA2611673A CA2611673C (en) | 2005-06-10 | 2006-06-07 | Vapor phase hydrogen peroxide deodorizer |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/149,360 | 2005-06-10 | ||
US11/149,360 US20060280665A1 (en) | 2005-06-10 | 2005-06-10 | Vapor phase hydrogen peroxide deodorizer |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006135620A1 true WO2006135620A1 (en) | 2006-12-21 |
Family
ID=36938528
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/022027 WO2006135620A1 (en) | 2005-06-10 | 2006-06-07 | Vapor phase hydrogen peroxide deodorizer |
Country Status (6)
Country | Link |
---|---|
US (1) | US20060280665A1 (en) |
EP (1) | EP1901785A1 (en) |
JP (2) | JP2008543369A (en) |
AU (1) | AU2006258117B2 (en) |
CA (1) | CA2611673C (en) |
WO (1) | WO2006135620A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009064453A1 (en) * | 2007-11-15 | 2009-05-22 | S. C. Johnson & Son, Inc. | Reduction of airborne malodors using hydrogen peroxide and a catalyst-coated media |
WO2014149321A1 (en) | 2013-03-15 | 2014-09-25 | American Sterilizer Company | Reactive surface coating having chemical decontamination and biocidal properties |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2175894B1 (en) * | 2007-08-07 | 2013-04-10 | Lee Antimicrobial Solutions LLC | Uv air treatment method and device |
US20090263499A1 (en) * | 2008-04-18 | 2009-10-22 | Ethicon, Inc. | Area decontamination via low-level concentration of germicidal agent |
ITBO20080418A1 (en) * | 2008-06-30 | 2010-01-01 | Patents Expl Company B V | METHOD FOR DISINFECTION OF AN ENVIRONMENT AND ITEMS CONTAINED IN IT AND DISINFECTIVE COMPOSITION. |
EP2179748B1 (en) * | 2008-10-27 | 2013-08-14 | The Procter & Gamble Company | Deodorizing system |
EP2179747A1 (en) * | 2008-10-27 | 2010-04-28 | The Procter & Gamble Company | Method of reducing malodors |
US9149550B2 (en) | 2012-10-02 | 2015-10-06 | Innovasource, Llc | Air and fabric freshener |
WO2015139075A1 (en) | 2014-03-18 | 2015-09-24 | Coolsan Hygiene Solutions Pty Ltd | Storage product and method |
US11305301B2 (en) | 2017-04-10 | 2022-04-19 | The Procter & Gamble Company | Microfluidic delivery device for dispensing and redirecting a fluid composition in the air |
US11691162B2 (en) | 2017-04-10 | 2023-07-04 | The Procter & Gamble Company | Microfluidic delivery cartridge for use with a microfluidic delivery device |
US20180296719A1 (en) * | 2017-04-18 | 2018-10-18 | The Procter & Gamble Company | Air freshening device utilizing a solid-form composition and a method of freshening the air |
US10806816B2 (en) | 2018-05-15 | 2020-10-20 | The Procter & Gamble Company | Microfluidic cartridge and microfluidic delivery device comprising the same |
JP7360122B2 (en) * | 2019-07-17 | 2023-10-12 | 株式会社テクノ菱和 | Hydrogen peroxide gas generator and hydrogen peroxide gas generation method |
CN115397743A (en) * | 2020-03-27 | 2022-11-25 | 阿科玛股份有限公司 | Device for releasing water and antimicrobial vapours into enclosed or partially enclosed spaces |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4107268A (en) * | 1976-07-09 | 1978-08-15 | Fmc Corporation | Animal confinement environment control |
EP0164818A2 (en) * | 1984-06-12 | 1985-12-18 | Nu Tech Ventures, Ltd. | Process for counteracting pungency of ammoniacal substances |
US5071622A (en) * | 1989-09-15 | 1991-12-10 | E. I. Du Pont De Nemours And Company | Process for odor control |
EP1029552A1 (en) * | 1999-02-18 | 2000-08-23 | Arconia GmbH | Agent, method, utilisation and apparatus for biological disinfection of air and rooms with air |
EP1393629A1 (en) * | 2002-08-29 | 2004-03-03 | Tevan B.V. | Aqueous disinfecting compositions based on quaternary ammonium monomers |
WO2004035718A2 (en) * | 2002-10-14 | 2004-04-29 | Arconia Gmbh | Composition |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4036994A (en) * | 1975-03-21 | 1977-07-19 | H.G.C. Construction & Equipment Company, Inc. | Method for abating odor and smoke emissions in the vapor exhaust from a meat broiling grill |
JPS5816899B2 (en) * | 1975-06-13 | 1983-04-02 | ニホンパ−オキサイド カブシキガイシヤ | Datsushi Yuzai |
FR2498083B1 (en) * | 1981-01-19 | 1986-05-23 | Charbonnages De France | |
JPS5953314A (en) * | 1982-09-17 | 1984-03-28 | Mazda Motor Corp | Pool conveyer |
JPS59120158A (en) * | 1982-12-28 | 1984-07-11 | アキレス株式会社 | Deodorant |
US4909999A (en) * | 1987-07-06 | 1990-03-20 | American Sterilizer Company | Flow-through vapor phase sterilization system |
JPS6487503A (en) * | 1987-09-28 | 1989-03-31 | Shikoku Chem | Composition slowly releasing active oxygen |
US5207877A (en) * | 1987-12-28 | 1993-05-04 | Electrocinerator Technologies, Inc. | Methods for purification of air |
US5137687A (en) * | 1989-09-15 | 1992-08-11 | E. I. Du Pont De Nemours And Company | Process for odor control |
US5258162A (en) * | 1989-11-07 | 1993-11-02 | Tetra Alfa Holdings S.A. | Method of producing a gaseous hydrogen peroxide-containing sterilization fluid |
JP3197371B2 (en) * | 1992-11-04 | 2001-08-13 | 稲畑香料株式会社 | Peracetic acid-based germicidal composition having an aroma and bleach composition |
US5674450A (en) * | 1994-04-28 | 1997-10-07 | Johnson & Johnson Medical, Inc. | Vapor sterilization using a non-aqueous source of hydrogen peroxide |
US6055679A (en) * | 1995-03-03 | 2000-05-02 | S. C. Johnson & Son, Inc. | Passive lavatory cleanser dispensing system |
JP3899139B2 (en) * | 1995-12-06 | 2007-03-28 | ジョンソン株式会社 | Deodorant composition for air conditioner |
TW343923B (en) * | 1996-01-22 | 1998-11-01 | Duskin Co Ltd | Deodorization/odor-removal/disinfection method and deodorization/odor-removal/disinfection apparatus |
US5820841A (en) * | 1996-09-19 | 1998-10-13 | Ethicon, Inc. | Hydrogen peroxide complexes of inorganic salts and synthesis thereof |
US5779973A (en) * | 1997-04-01 | 1998-07-14 | Steris Corporation | Vapor phase interstitial microbial decontamination of overwrapped IV bags |
US6039922A (en) * | 1997-08-15 | 2000-03-21 | Tetra Laval Holdings & Finance, Sa | UV radiation and vapor-phase hydrogen peroxide sterilization packaging |
US6495096B1 (en) * | 1998-07-30 | 2002-12-17 | Mitsubishi Gas Chemical Company, Inc. | Deodorant and process for deodorization using said deodorant |
US6365099B1 (en) * | 1998-11-12 | 2002-04-02 | Fmc Corporation | In situ gas scrubbing method and system for odor and corrosion control in wastewater collection systems |
JP2001170147A (en) * | 1999-12-17 | 2001-06-26 | Toshiko Takatomi | Method for clarifying indoor air |
US6815408B2 (en) * | 2002-02-11 | 2004-11-09 | Paul C. Wegner | Hydrogen peroxide stabilizer and resulting product and applications |
US7029588B2 (en) * | 2003-03-19 | 2006-04-18 | Samuel Rupert Owens | Oxidizing solution and process for contaminants |
-
2005
- 2005-06-10 US US11/149,360 patent/US20060280665A1/en not_active Abandoned
-
2006
- 2006-06-07 EP EP06772367A patent/EP1901785A1/en not_active Withdrawn
- 2006-06-07 AU AU2006258117A patent/AU2006258117B2/en not_active Ceased
- 2006-06-07 CA CA2611673A patent/CA2611673C/en not_active Expired - Fee Related
- 2006-06-07 JP JP2008515849A patent/JP2008543369A/en not_active Withdrawn
- 2006-06-07 WO PCT/US2006/022027 patent/WO2006135620A1/en active Application Filing
-
2012
- 2012-06-28 JP JP2012145443A patent/JP2012236037A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4107268A (en) * | 1976-07-09 | 1978-08-15 | Fmc Corporation | Animal confinement environment control |
EP0164818A2 (en) * | 1984-06-12 | 1985-12-18 | Nu Tech Ventures, Ltd. | Process for counteracting pungency of ammoniacal substances |
US5071622A (en) * | 1989-09-15 | 1991-12-10 | E. I. Du Pont De Nemours And Company | Process for odor control |
EP1029552A1 (en) * | 1999-02-18 | 2000-08-23 | Arconia GmbH | Agent, method, utilisation and apparatus for biological disinfection of air and rooms with air |
EP1393629A1 (en) * | 2002-08-29 | 2004-03-03 | Tevan B.V. | Aqueous disinfecting compositions based on quaternary ammonium monomers |
WO2004035718A2 (en) * | 2002-10-14 | 2004-04-29 | Arconia Gmbh | Composition |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009064453A1 (en) * | 2007-11-15 | 2009-05-22 | S. C. Johnson & Son, Inc. | Reduction of airborne malodors using hydrogen peroxide and a catalyst-coated media |
US8071081B2 (en) | 2007-11-15 | 2011-12-06 | S.C. Johnson & Son, Inc. | Reduction of airborne malodors using hydrogen peroxide and a catalyst-coated media |
WO2014149321A1 (en) | 2013-03-15 | 2014-09-25 | American Sterilizer Company | Reactive surface coating having chemical decontamination and biocidal properties |
US9353269B2 (en) | 2013-03-15 | 2016-05-31 | American Sterilizer Company | Reactive surface coating having chemical decontamination and biocidal properties |
US10017650B2 (en) | 2013-03-15 | 2018-07-10 | American Sterilizer Company | Reactive surface coating having chemical decontamination and biocidal properties |
US10501644B2 (en) | 2013-03-15 | 2019-12-10 | American Sterilizer Company | Reactive surface coating having chemical decontamination and biocidal properties |
Also Published As
Publication number | Publication date |
---|---|
US20060280665A1 (en) | 2006-12-14 |
AU2006258117A1 (en) | 2006-12-21 |
JP2008543369A (en) | 2008-12-04 |
AU2006258117B2 (en) | 2010-08-26 |
JP2012236037A (en) | 2012-12-06 |
EP1901785A1 (en) | 2008-03-26 |
CA2611673A1 (en) | 2006-12-21 |
CA2611673C (en) | 2011-11-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2611673C (en) | Vapor phase hydrogen peroxide deodorizer | |
US8071081B2 (en) | Reduction of airborne malodors using hydrogen peroxide and a catalyst-coated media | |
KR101343716B1 (en) | - metal ion-modified materials for odour removal and control | |
US8298482B2 (en) | Vapor phase hydrogen peroxide deodorizer | |
JP2008297507A (en) | Cleaning agent | |
JP2001316213A (en) | Disinfecting deodorizer | |
MX2008005424A (en) | Treatment of odors using nanocrystalline metal oxides. | |
KR101605114B1 (en) | Method of manufacturing eco-friendly deodorant included Wasabia koreana for removing sick house syndrome | |
JP2006149892A (en) | Composition for suppressing urine odor | |
US20070272895A1 (en) | Deodorizing system | |
JP2004285485A (en) | Treating agent for textile product for deodorizing processing comprising granular adsorbent | |
KR101707793B1 (en) | Deodorizing agent for removal of ammonia and deodorization filter comprising the same | |
JP2007252777A (en) | Volatile substance-volatilization adjusting material, volatile substance-volatilization adjusting filter medium, volatile substance-volatilization controlling method and volatile substance-volatilization controlling device | |
JP2012024537A (en) | Polymeric deodorant composition | |
JPH0739749A (en) | Air cleaning agent to be put in space and air cleaning method | |
JP2745424B2 (en) | Deodorant | |
JP4115670B2 (en) | Fragrance composition containing odor neutralizer | |
CA2351625A1 (en) | Spray containing amphoteric material to reduce malodors | |
JPH01238866A (en) | Deodorizer | |
KR101820297B1 (en) | Deodorizing agent for removal of valeric acid and deodorization filter comprising the same | |
JPH03251253A (en) | Deodorant | |
KR100480808B1 (en) | Low aldehydes removing methods for prevention of sick house syndrome and multiple chemical sensitivity | |
JP2002263178A (en) | Stationary deodorant | |
JP2006149893A (en) | Urine odor suppressing method | |
JP3050507U (en) | Deodorant package |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Country of ref document: MX Ref document number: MX/a/2007/015616 |
|
ENP | Entry into the national phase |
Ref document number: 2611673 Country of ref document: CA Ref document number: 2008515849 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
REEP | Request for entry into the european phase |
Ref document number: 2006772367 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006772367 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006258117 Country of ref document: AU |
|
ENP | Entry into the national phase |
Ref document number: 2006258117 Country of ref document: AU Date of ref document: 20060607 Kind code of ref document: A |