NO323014B1 - Biocidsammensetninger og fremgangsmater for a behandle vandige systemer. - Google Patents
Biocidsammensetninger og fremgangsmater for a behandle vandige systemer. Download PDFInfo
- Publication number
- NO323014B1 NO323014B1 NO20003267A NO20003267A NO323014B1 NO 323014 B1 NO323014 B1 NO 323014B1 NO 20003267 A NO20003267 A NO 20003267A NO 20003267 A NO20003267 A NO 20003267A NO 323014 B1 NO323014 B1 NO 323014B1
- Authority
- NO
- Norway
- Prior art keywords
- thp
- surfactant
- biopenetrant
- water
- composition according
- Prior art date
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- 230000003115 biocidal effect Effects 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 title claims description 54
- 238000000034 method Methods 0.000 title claims description 16
- 239000004094 surface-active agent Substances 0.000 claims abstract description 46
- 230000002195 synergetic effect Effects 0.000 claims abstract description 14
- 229920001577 copolymer Polymers 0.000 claims abstract description 11
- 229920000642 polymer Polymers 0.000 claims abstract description 9
- 125000001453 quaternary ammonium group Chemical group 0.000 claims abstract description 9
- -1 polyethylene Polymers 0.000 claims description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 13
- 239000000243 solution Substances 0.000 claims description 10
- 239000004202 carbamide Substances 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- 239000013543 active substance Substances 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 5
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 5
- 230000000813 microbial effect Effects 0.000 claims description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 150000003973 alkyl amines Chemical class 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 238000011109 contamination Methods 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 125000006353 oxyethylene group Chemical group 0.000 claims description 4
- 229920000768 polyamine Polymers 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 3
- 150000003457 sulfones Chemical class 0.000 claims description 3
- 239000012747 synergistic agent Substances 0.000 claims description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 125000005228 aryl sulfonate group Chemical group 0.000 claims description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 2
- 125000000962 organic group Chemical group 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 229940124530 sulfonamide Drugs 0.000 claims description 2
- 150000003456 sulfonamides Chemical class 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000003139 biocide Substances 0.000 abstract description 17
- 239000003752 hydrotrope Substances 0.000 abstract description 9
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 abstract description 4
- JMXMXKRNIYCNRV-UHFFFAOYSA-N bis(hydroxymethyl)phosphanylmethanol Chemical compound OCP(CO)CO JMXMXKRNIYCNRV-UHFFFAOYSA-N 0.000 abstract description 2
- FAUOSXUSCVJWAY-UHFFFAOYSA-N tetrakis(hydroxymethyl)phosphanium Chemical class OC[P+](CO)(CO)CO FAUOSXUSCVJWAY-UHFFFAOYSA-N 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 50
- 150000003839 salts Chemical class 0.000 description 19
- 125000004432 carbon atom Chemical group C* 0.000 description 17
- 241000894006 Bacteria Species 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 12
- 239000003093 cationic surfactant Substances 0.000 description 11
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 10
- 238000005187 foaming Methods 0.000 description 8
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 239000003945 anionic surfactant Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 6
- 239000002736 nonionic surfactant Substances 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 125000002877 alkyl aryl group Chemical group 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 5
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- 125000004437 phosphorous atom Chemical group 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- 101100288310 Arabidopsis thaliana KTI2 gene Proteins 0.000 description 4
- 102000008186 Collagen Human genes 0.000 description 4
- 108010035532 Collagen Proteins 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 229920001436 collagen Polymers 0.000 description 4
- 239000000498 cooling water Substances 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- YIEDHPBKGZGLIK-UHFFFAOYSA-L tetrakis(hydroxymethyl)phosphanium;sulfate Chemical compound [O-]S([O-])(=O)=O.OC[P+](CO)(CO)CO.OC[P+](CO)(CO)CO YIEDHPBKGZGLIK-UHFFFAOYSA-L 0.000 description 4
- KMDMOMDSEVTJTI-UHFFFAOYSA-N 2-phosphonobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)P(O)(O)=O KMDMOMDSEVTJTI-UHFFFAOYSA-N 0.000 description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 3
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 3
- 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 3
- 229940123973 Oxygen scavenger Drugs 0.000 description 3
- 229940072056 alginate Drugs 0.000 description 3
- 235000010443 alginic acid Nutrition 0.000 description 3
- 229920000615 alginic acid Polymers 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 150000008051 alkyl sulfates Chemical class 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 239000002280 amphoteric surfactant Substances 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- MRVZORUPSXTRHD-UHFFFAOYSA-N bis(hydroxymethyl)phosphorylmethanol Chemical compound OCP(=O)(CO)CO MRVZORUPSXTRHD-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
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- 239000003760 tallow Substances 0.000 description 3
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 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 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- 239000001263 FEMA 3042 Substances 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
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- 229910019142 PO4 Inorganic materials 0.000 description 2
- 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 2
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- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
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- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 description 2
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- CYFLXLSBHQBMFT-UHFFFAOYSA-N sulfamoxole Chemical group O1C(C)=C(C)N=C1NS(=O)(=O)C1=CC=C(N)C=C1 CYFLXLSBHQBMFT-UHFFFAOYSA-N 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
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- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-UHFFFAOYSA-N 2-(1,2-dihydroxyethyl)oxolane-3,4-diol Polymers OCC(O)C1OCC(O)C1O JNYAEWCLZODPBN-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
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- 125000000542 sulfonic acid group Chemical group 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/34—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-halogen bonds; Phosphonium salts
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/02—Non-contaminated water, e.g. for industrial water supply
- C02F2103/023—Water in cooling circuits
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Environmental & Geological Engineering (AREA)
- Hydrology & Water Resources (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9727006.0A GB9727006D0 (en) | 1997-12-23 | 1997-12-23 | Biocidal compositions and treatments |
| GBGB9805407.5A GB9805407D0 (en) | 1998-03-14 | 1998-03-14 | Biocidal compositions and treatments |
| GBGB9805746.6A GB9805746D0 (en) | 1998-03-19 | 1998-03-19 | Biocidal compositions and treatments |
| GBGB9811778.1A GB9811778D0 (en) | 1998-06-03 | 1998-06-03 | Biocidal compositions and treatments |
| GBGB9820255.9A GB9820255D0 (en) | 1998-09-18 | 1998-09-18 | Biocidal compositions and treatments |
| PCT/EP1998/008394 WO1999033345A1 (en) | 1997-12-23 | 1998-12-21 | Biocidal compositions and treatments |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20003267D0 NO20003267D0 (no) | 2000-06-22 |
| NO20003267L NO20003267L (no) | 2000-08-02 |
| NO323014B1 true NO323014B1 (no) | 2006-12-27 |
Family
ID=27517441
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20003267A NO323014B1 (no) | 1997-12-23 | 2000-06-22 | Biocidsammensetninger og fremgangsmater for a behandle vandige systemer. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6784168B1 (ja) |
| EP (1) | EP1041885B1 (ja) |
| JP (1) | JP4814425B2 (ja) |
| KR (1) | KR100542669B1 (ja) |
| AT (1) | ATE226393T1 (ja) |
| AU (1) | AU736266B2 (ja) |
| CA (1) | CA2316363C (ja) |
| DE (1) | DE69808968T2 (ja) |
| DK (1) | DK1041885T3 (ja) |
| NO (1) | NO323014B1 (ja) |
| NZ (1) | NZ505301A (ja) |
| PT (1) | PT1041885E (ja) |
| TW (1) | TW492840B (ja) |
| WO (1) | WO1999033345A1 (ja) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0001417D0 (en) | 2000-01-22 | 2000-03-08 | Albright & Wilson Uk Ltd | Bleaching pulp |
| GB0017675D0 (en) * | 2000-07-20 | 2000-09-06 | Rhodia Cons Spec Ltd | Treatment of iron sulphide deposits |
| GB0301975D0 (en) | 2003-01-29 | 2003-02-26 | Rhodia Cons Spec Ltd | Treating slurries |
| GB0306531D0 (en) * | 2003-03-21 | 2003-04-23 | Rhodia Cons Spec Ltd | Formulation for corrosion and scale inhibition |
| US7867479B2 (en) * | 2003-11-14 | 2011-01-11 | Bug Buster, Ltd. | Compounds to affect insect behavior and/or bird behavior |
| US7780859B2 (en) | 2003-06-20 | 2010-08-24 | Rhodia Operations | Uncoupling agents |
| GB0402395D0 (en) * | 2004-02-03 | 2004-03-10 | Rhodia Cons Spec Ltd | Synergistic biocidal compositions |
| CA2570219A1 (en) * | 2004-06-21 | 2005-12-29 | Rhodia Uk Limited | Improvement of sludge quality |
| GB0427692D0 (en) * | 2004-12-17 | 2005-01-19 | Rhodia Cons Spec Ltd | Improvement of sludge quality |
| JP4628037B2 (ja) * | 2004-08-06 | 2011-02-09 | ケイ・アイ化成株式会社 | 水処理用の環境応力亀裂の防止方法 |
| EP3563688A1 (en) | 2005-11-28 | 2019-11-06 | DSM IP Assets B.V. | Enzyme preparations yielding a clean taste |
| US20080142453A1 (en) * | 2006-12-13 | 2008-06-19 | Michael Joseph Unhoch | Biocidal composition and method for treating recirculating water systems |
| WO2008116036A1 (en) * | 2007-03-21 | 2008-09-25 | Dow Global Technologies Inc. | Hair care composition |
| JP5368443B2 (ja) * | 2007-07-24 | 2013-12-18 | ダウ グローバル テクノロジーズ エルエルシー | 水系流体及び水系流体と共に用いられるシステム中の微生物濃度の増大を低減及び抑制するための方法及び配合物 |
| WO2009015089A2 (en) * | 2007-07-24 | 2009-01-29 | Dow Global Technologies Inc. | Methods of and formulations for reducing and inhibiting the growth of the concentration of microbes in water-based fluids and systems used with them |
| KR100947905B1 (ko) * | 2007-08-08 | 2010-03-17 | 윤대식 | 레지오넬라속균 방제용 조성물 |
| US8778370B2 (en) * | 2009-01-16 | 2014-07-15 | Sterilex Corporation | Method and composition for inhibiting growth of microorganisms in industrial process waters in the presence of anionic anti-fouling additives |
| UA106606C2 (uk) | 2009-03-16 | 2014-09-25 | Родія Оперейшнс | Стабілізована біоцидна композиція |
| CN103340212A (zh) | 2009-10-20 | 2013-10-09 | 陶氏环球技术有限公司 | 协同抗微生物组合物 |
| US20110195938A1 (en) * | 2010-02-09 | 2011-08-11 | Baker Hughes Incorporated | Process for preventing or mitigating biofouling |
| US10174239B2 (en) | 2010-02-09 | 2019-01-08 | Baker Hughes, A Ge Company, Llc | Process for preventing or mitigating biofouling |
| GB2488768A (en) | 2011-03-07 | 2012-09-12 | Rhodia Operations | Treatment of hydrocarbon-containing systems |
| PL2736328T3 (pl) | 2011-09-15 | 2016-06-30 | Dow Global Technologies Llc | Biocydowe kompozycje oraz sposoby stosowania |
| EA027108B1 (ru) * | 2011-09-23 | 2017-06-30 | Лонца Инк. | Способ и композиция для удаления сульфида водорода из промышленных текучих сред |
| PL2736339T3 (pl) | 2011-10-13 | 2016-01-29 | Dow Global Technologies Llc | Biocydowe kompozycje oraz sposoby stosowania |
| ES2861300T3 (es) * | 2012-02-20 | 2021-10-06 | Basf Se | Potenciación de la actividad antimicrobiana de biocidas con polímeros |
| US9752083B2 (en) | 2012-08-21 | 2017-09-05 | Lonza, Inc. | Method of scavenging hydrogen sulfide and/or sulfhydryl compounds |
| WO2016134873A1 (en) | 2015-02-27 | 2016-09-01 | Clariant International Ltd | Liquid dissolver composition, a method for its preparation and its application in metal sulfide removal |
| US10633573B2 (en) * | 2015-04-02 | 2020-04-28 | Clariant International Ltd. | Composition and method for inhibition of sulfide scales |
| BR112017020781A2 (pt) * | 2015-04-02 | 2018-06-26 | Clariant Int Ltd | composição e método para inibição de escalas de sulfeto |
| US10161824B2 (en) * | 2015-05-11 | 2018-12-25 | HilFlo, LLC | Hydrostatic pressure test method and apparatus |
| US10214684B2 (en) | 2015-09-30 | 2019-02-26 | Bwa Water Additives Uk Limited | Friction reducers and well treatment fluids |
| CN105211065A (zh) * | 2015-11-03 | 2016-01-06 | 天津亿利科能源科技发展股份有限公司 | 高温srb杀菌剂及其制备方法 |
| CN110036056B (zh) | 2016-12-14 | 2022-09-13 | 埃科莱布美国股份有限公司 | 季阳离子聚合物 |
| WO2019241056A1 (en) | 2018-06-12 | 2019-12-19 | Ecolab Usa Inc. | Quaternary cationic surfactants and polymers for use as release and coating modifying agents in creping and tissue papers |
| DK3856867T3 (en) | 2018-09-28 | 2022-07-04 | Rhodia Operations | Treatment of iron sulphide deposits |
| EP3711485A1 (en) | 2019-03-19 | 2020-09-23 | Rhodia Operations | Synergistic biocidal compositions and methods for using same |
| EP3711486A1 (en) | 2019-03-19 | 2020-09-23 | Rhodia Operations | Biocidal compositions including a phosphonium quaternary cationic surfactant and methods for using same |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3644083A (en) * | 1970-04-09 | 1972-02-22 | American Cyanamid Co | Durable flame retardant finish for cellulosic textile materials |
| US4602011A (en) * | 1975-10-24 | 1986-07-22 | Chapman Chemical Company | Antimicrobial compositions and methods of using same |
| US4599372A (en) * | 1983-07-25 | 1986-07-08 | Diamond Shamrock Chemicals Company | Self-inverting water-in-oil polymer emulsions having low pour point temperatures |
| DE3469162D1 (en) * | 1983-08-26 | 1988-03-10 | Albright & Wilson | Biocidal water treatment |
| GB8323025D0 (en) * | 1983-08-26 | 1983-09-28 | Albright & Wilson | Biocidal water treatment |
| AU597894B2 (en) * | 1985-08-06 | 1990-06-14 | Albright & Wilson Uk Limited | Biocidal mixtures of organophosphines and surfactants |
| GB8904274D0 (en) * | 1989-02-24 | 1989-04-12 | Albright & Wilson | Biocidal compositions and treatments |
| JP2847164B2 (ja) * | 1989-05-19 | 1999-01-13 | ダウコーニングアジア株式会社 | 繊維体用抗菌剤 |
| BE1003510A5 (fr) * | 1989-10-09 | 1992-04-07 | Fabricom Air Conditioning Sa | Composition desinfectante et procede de desinfection. |
| US5145643A (en) * | 1990-01-05 | 1992-09-08 | Allergan, Inc. | Nonoxidative ophthalmic compositions and methods for preserving and using same |
| CA2057822C (en) * | 1990-12-18 | 1998-04-21 | Keith Philip Davis | Water treatment agent |
| GB2257043A (en) | 1991-04-10 | 1993-01-06 | Albright & Wilson | Fungicidal wood treatment using hydroxyalkyl phosphines |
| EP0766729B1 (en) * | 1994-06-20 | 1999-11-03 | Unilever Plc | Improvements relating to antimicrobial cleaning compositions |
| BR9509598A (pt) * | 1994-11-04 | 1998-01-06 | Betzdearborn Inc | Composição microbiocida processo para inibir ou controlar o crescimento e e a deposição de organismos formadores de lodo em sistemas aquosos e combinação microbiocida de materiais |
-
1998
- 1998-12-21 CA CA002316363A patent/CA2316363C/en not_active Expired - Lifetime
- 1998-12-21 NZ NZ505301A patent/NZ505301A/en not_active IP Right Cessation
- 1998-12-21 AT AT98966392T patent/ATE226393T1/de active
- 1998-12-21 DK DK98966392T patent/DK1041885T3/da active
- 1998-12-21 KR KR1020007007053A patent/KR100542669B1/ko not_active IP Right Cessation
- 1998-12-21 PT PT98966392T patent/PT1041885E/pt unknown
- 1998-12-21 EP EP98966392A patent/EP1041885B1/en not_active Expired - Lifetime
- 1998-12-21 JP JP2000526119A patent/JP4814425B2/ja not_active Expired - Fee Related
- 1998-12-21 AU AU22753/99A patent/AU736266B2/en not_active Expired
- 1998-12-21 WO PCT/EP1998/008394 patent/WO1999033345A1/en active IP Right Grant
- 1998-12-21 DE DE69808968T patent/DE69808968T2/de not_active Expired - Lifetime
- 1998-12-21 US US09/582,152 patent/US6784168B1/en not_active Expired - Lifetime
- 1998-12-28 TW TW087121718A patent/TW492840B/zh not_active IP Right Cessation
-
2000
- 2000-06-22 NO NO20003267A patent/NO323014B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CA2316363C (en) | 2004-12-21 |
| JP2001527028A (ja) | 2001-12-25 |
| DE69808968T2 (de) | 2003-09-11 |
| NO20003267D0 (no) | 2000-06-22 |
| AU2275399A (en) | 1999-07-19 |
| WO1999033345A1 (en) | 1999-07-08 |
| TW492840B (en) | 2002-07-01 |
| PT1041885E (pt) | 2003-03-31 |
| NO20003267L (no) | 2000-08-02 |
| NZ505301A (en) | 2002-05-31 |
| KR100542669B1 (ko) | 2006-01-12 |
| AU736266B2 (en) | 2001-07-26 |
| CA2316363A1 (en) | 1999-07-08 |
| KR20010040308A (ko) | 2001-05-15 |
| EP1041885A1 (en) | 2000-10-11 |
| JP4814425B2 (ja) | 2011-11-16 |
| ATE226393T1 (de) | 2002-11-15 |
| DK1041885T3 (da) | 2003-02-17 |
| US6784168B1 (en) | 2004-08-31 |
| EP1041885B1 (en) | 2002-10-23 |
| DE69808968D1 (de) | 2002-11-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1K | Patent expired |