ZA200101939B - Method of controlling biofouling in aqueous media using antimicrobial emulsions. - Google Patents
Method of controlling biofouling in aqueous media using antimicrobial emulsions. Download PDFInfo
- Publication number
- ZA200101939B ZA200101939B ZA200101939A ZA200101939A ZA200101939B ZA 200101939 B ZA200101939 B ZA 200101939B ZA 200101939 A ZA200101939 A ZA 200101939A ZA 200101939 A ZA200101939 A ZA 200101939A ZA 200101939 B ZA200101939 B ZA 200101939B
- Authority
- ZA
- South Africa
- Prior art keywords
- oil
- group
- alkyl
- water emulsion
- aqueous medium
- Prior art date
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- 239000000839 emulsion Substances 0.000 title claims description 75
- 238000000034 method Methods 0.000 title claims description 49
- 230000000845 anti-microbial effect Effects 0.000 title claims description 27
- 239000012736 aqueous medium Substances 0.000 title claims description 27
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims description 60
- 210000004027 cell Anatomy 0.000 claims description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 239000003921 oil Substances 0.000 claims description 31
- -1 pevtachlorophenol Chemical compound 0.000 claims description 31
- 239000012071 phase Substances 0.000 claims description 29
- 239000007764 o/w emulsion Substances 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 239000008346 aqueous phase Substances 0.000 claims description 19
- 239000003995 emulsifying agent Substances 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 19
- 239000004530 micro-emulsion Substances 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 239000004599 antimicrobial Substances 0.000 claims description 10
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 239000008235 industrial water Substances 0.000 claims description 8
- 230000008685 targeting Effects 0.000 claims description 7
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 6
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 6
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 6
- 239000002280 amphoteric surfactant Substances 0.000 claims description 6
- 229960003237 betaine Drugs 0.000 claims description 6
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims description 6
- 239000002738 chelating agent Substances 0.000 claims description 6
- BFMYDTVEBKDAKJ-UHFFFAOYSA-L disodium;(2',7'-dibromo-3',6'-dioxido-3-oxospiro[2-benzofuran-1,9'-xanthene]-4'-yl)mercury;hydrate Chemical compound O.[Na+].[Na+].O1C(=O)C2=CC=CC=C2C21C1=CC(Br)=C([O-])C([Hg])=C1OC1=C2C=C(Br)C([O-])=C1 BFMYDTVEBKDAKJ-UHFFFAOYSA-L 0.000 claims description 6
- 150000002334 glycols Chemical class 0.000 claims description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 6
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 5
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- 239000003945 anionic surfactant Substances 0.000 claims description 5
- 239000003093 cationic surfactant Substances 0.000 claims description 5
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- 229910052708 sodium Inorganic materials 0.000 claims description 5
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- 229920001577 copolymer Polymers 0.000 claims description 4
- UUIVKBHZENILKB-UHFFFAOYSA-N 2,2-dibromo-2-cyanoacetamide Chemical compound NC(=O)C(Br)(Br)C#N UUIVKBHZENILKB-UHFFFAOYSA-N 0.000 claims description 3
- BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
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- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 claims description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 3
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 3
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 claims description 3
- KTYVHLCLTPLSGC-UHFFFAOYSA-N amino propanoate Chemical compound CCC(=O)ON KTYVHLCLTPLSGC-UHFFFAOYSA-N 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 3
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 claims description 3
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 claims description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- 150000002462 imidazolines Chemical class 0.000 claims description 3
- JWZXKXIUSSIAMR-UHFFFAOYSA-N methylene bis(thiocyanate) Chemical compound N#CSCSC#N JWZXKXIUSSIAMR-UHFFFAOYSA-N 0.000 claims description 3
- 239000002480 mineral oil Substances 0.000 claims description 3
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000004306 orthophenyl phenol Substances 0.000 claims description 3
- 235000010292 orthophenyl phenol Nutrition 0.000 claims description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 3
- 230000002441 reversible effect Effects 0.000 claims description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 3
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 claims description 3
- TYLSDQJYPYQCRK-UHFFFAOYSA-N sulfo 4-amino-4-oxobutanoate Chemical compound NC(=O)CCC(=O)OS(O)(=O)=O TYLSDQJYPYQCRK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004711 α-olefin Substances 0.000 claims description 3
- SKDNDVDHYMEGNJ-UHFFFAOYSA-N (2-bromo-2-nitroethenyl)benzene Chemical compound [O-][N+](=O)C(Br)=CC1=CC=CC=C1 SKDNDVDHYMEGNJ-UHFFFAOYSA-N 0.000 claims description 2
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 claims description 2
- 239000004907 Macro-emulsion Substances 0.000 claims description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 claims description 2
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Chemical class 0.000 claims 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 2
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- 150000003457 sulfones Chemical class 0.000 claims 2
- AXVXPQXJQJZFGV-UHFFFAOYSA-N 5-chloro-2-(2,3-dichlorophenoxy)phenol Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=CC(Cl)=C1Cl AXVXPQXJQJZFGV-UHFFFAOYSA-N 0.000 claims 1
- 239000005725 8-Hydroxyquinoline Substances 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
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- 150000003014 phosphoric acid esters Chemical class 0.000 claims 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 239000003139 biocide Substances 0.000 description 28
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 26
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 20
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- 238000007792 addition Methods 0.000 description 11
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 11
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- 230000004151 fermentation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000000799 fluorescence microscopy Methods 0.000 description 1
- 238000005558 fluorometry Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940124561 microbicide Drugs 0.000 description 1
- 239000006151 minimal media Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000007793 ph indicator Substances 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
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229940048842 sodium xylenesulfonate Drugs 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 229940071127 thioglycolate Drugs 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- YBNLWIZAWPBUKQ-UHFFFAOYSA-N trichloro(trichloromethylsulfonyl)methane Chemical compound ClC(Cl)(Cl)S(=O)(=O)C(Cl)(Cl)Cl YBNLWIZAWPBUKQ-UHFFFAOYSA-N 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 238000003260 vortexing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 229940071104 xylenesulfonate Drugs 0.000 description 1
Classifications
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/151,637 US6096225A (en) | 1998-09-11 | 1998-09-11 | Method of controlling biofouling in aqueous media using antimicrobial emulsions |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200101939B true ZA200101939B (en) | 2001-10-02 |
Family
ID=22539616
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200101939A ZA200101939B (en) | 1998-09-11 | 1999-06-25 | Method of controlling biofouling in aqueous media using antimicrobial emulsions. |
Country Status (16)
Country | Link |
---|---|
US (1) | US6096225A (es) |
EP (1) | EP1113995A4 (es) |
JP (1) | JP2002524257A (es) |
KR (1) | KR20010073148A (es) |
CN (1) | CN1316979A (es) |
AR (1) | AR021218A1 (es) |
AU (1) | AU4834099A (es) |
BR (1) | BR9913586A (es) |
CA (1) | CA2342242A1 (es) |
CO (1) | CO5221043A1 (es) |
ID (1) | ID28347A (es) |
NO (1) | NO20011225L (es) |
NZ (1) | NZ510364A (es) |
TW (1) | TW533190B (es) |
WO (1) | WO2000015562A1 (es) |
ZA (1) | ZA200101939B (es) |
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US6514458B1 (en) * | 2000-02-25 | 2003-02-04 | Ge Betz, Inc. | Method for removing microbes from surfaces |
EP1272433B1 (de) * | 2000-03-16 | 2004-01-02 | TFM Handels AG | Schwefelfreies lignin und dessen derivate zur herabsetzung der bildung von schleim und ablagerungen in industriellen anlagen |
US6267897B1 (en) * | 2000-05-04 | 2001-07-31 | Nalco Chemical Company | Method of inhibiting biofilm formation in commercial and industrial water systems |
WO2001094513A1 (en) | 2000-06-05 | 2001-12-13 | S. C. Johnson & Son, Inc. | Biocidal cleaner composition |
US6379720B1 (en) * | 2000-07-18 | 2002-04-30 | Nalco Chemical Company | Compositions containing hops extract and their use in water systems and process streams to control biological fouling |
US7262222B2 (en) * | 2002-01-17 | 2007-08-28 | Verichem, Inc. | Synergistic mixtures of o-phenylphenol and other nitrogen and aldehyde microbiocides |
US20100160445A1 (en) * | 2002-01-17 | 2010-06-24 | Carlson Paul E | Synergistic Mixtures of OPP and DGH |
DE10309425B4 (de) * | 2003-03-05 | 2010-12-30 | Bk Giulini Gmbh | Mikrobizid zur Desinfektion von industriellen Wasserkreisläufen |
US20060124246A1 (en) * | 2004-12-14 | 2006-06-15 | Pitney Bowes Incorporated | Moistening fluids that destroy and/or inhibit the growth of biological organisms |
US7258878B2 (en) * | 2004-12-20 | 2007-08-21 | Kimberly-Clark Worldwide, Inc. | Anti-microbial composition and methods of use thereof |
WO2008048350A2 (en) * | 2006-02-24 | 2008-04-24 | Nanovibronix Inc. | System and method for surface acoustic wave treatment of skin |
US20080286235A1 (en) * | 2006-02-28 | 2008-11-20 | Beierle John W Jack | Antimicrobials and related methods |
FI119903B (fi) * | 2006-03-16 | 2009-05-15 | Kemira Oyj | Bakteeri-itiöiden muodostumisen estäminen kartonkikoneen hylkysysteemissä |
CN101037554B (zh) * | 2006-03-16 | 2013-06-12 | 罗门哈斯公司 | 包囊的生物杀伤剂的混合物 |
JP2008100964A (ja) * | 2006-10-20 | 2008-05-01 | Kao Corp | バイオフィルム生成抑制剤組成物 |
EP1993355B1 (en) * | 2006-03-23 | 2017-10-11 | Kao Corporation | Biofilm formation inhibitor composition |
JP4972375B2 (ja) * | 2006-10-20 | 2012-07-11 | 花王株式会社 | バイオフィルム生成抑制剤組成物 |
JP5209864B2 (ja) * | 2006-10-20 | 2013-06-12 | 花王株式会社 | バイオフィルム生成抑制剤組成物 |
KR20080111155A (ko) * | 2006-04-21 | 2008-12-22 | 가오 가부시키가이샤 | 바이오필름 제어제 조성물 |
JP5322400B2 (ja) * | 2006-04-21 | 2013-10-23 | 花王株式会社 | バイオフィルム制御剤組成物 |
EP2120561A4 (en) | 2007-02-19 | 2012-11-21 | Plurogen Therapeutics Inc | COMPOSITIONS FOR TREATING BIOFILMS, AND METHODS FOR THEIR USE |
MY169583A (en) * | 2007-06-28 | 2019-04-22 | Dow Brasil Sudeste Ind Ltda | Control of bacteria in fermentation processes |
JP5162191B2 (ja) * | 2007-09-25 | 2013-03-13 | 花王株式会社 | 皮膚外用剤 |
JP5166808B2 (ja) * | 2007-09-25 | 2013-03-21 | 花王株式会社 | 洗浄機内のバイオフィルム生成抑制方法 |
US20100158852A1 (en) * | 2008-12-22 | 2010-06-24 | Wilson Kurt Whitekettle | Method for reduction of microbes on surfaces |
JP5181354B2 (ja) * | 2009-03-31 | 2013-04-10 | 学校法人神奈川大学 | 防腐防黴剤エマルション |
WO2010135449A1 (en) | 2009-05-19 | 2010-11-25 | Plurogen Therapeutics, Inc. | Surface active agent compositions and methods for enhancing oxygenation, reducing bacteria and improving wound healing |
KR101294999B1 (ko) * | 2010-11-24 | 2013-08-09 | 주식회사셀세이프 | 세포의 마이코플라즈마 오염의 제거방법 |
CN112655707A (zh) | 2013-03-25 | 2021-04-16 | 凯米罗总公司 | 用于处理水的杀生物剂制剂和方法 |
JP6269672B2 (ja) * | 2013-07-18 | 2018-01-31 | ライオン株式会社 | 口腔バイオフィルム除去剤及び口腔用組成物 |
CA2974361A1 (en) | 2015-01-20 | 2016-07-28 | Plurogen Therapeutics, Llc | Compositions and methods of treating microbes |
US10850999B2 (en) | 2015-04-24 | 2020-12-01 | Ecolab Usa Inc. | Submergible biocide reactor and method |
US11071301B2 (en) | 2016-10-21 | 2021-07-27 | Ecolab Usa Inc. | Anti-microbial agent to control biomass accumulation in SO2 scrubbers |
PT3450626T (pt) * | 2017-08-29 | 2020-07-31 | Univ Copenhagen | Método para controlar o crescimento de microorganismos e/ou biofilmes num processo industrial |
EP3450623B1 (en) | 2017-08-29 | 2023-06-28 | Kemira Oyj | Method for controlling growth of microorganisms and/or biofilms in an industrial process |
US10927397B2 (en) | 2018-10-16 | 2021-02-23 | Sterilex, Llc | Compositions, devices and methods for detecting biofilms |
US11932795B2 (en) | 2020-06-03 | 2024-03-19 | Ecolab Usa Inc. | Aromatic amine epoxide adducts for corrosion inhibition |
CA3181256A1 (en) | 2020-06-03 | 2021-12-09 | Sukhwan Soontravanich | Non-caustic cleaning methods and uses |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
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US3897562A (en) * | 1973-06-15 | 1975-07-29 | Betz Laboratories | 2,2-Dibromo-3-Nitrilo propionamide and pentachlorophenol as a slime control composition |
US4253877A (en) * | 1979-08-02 | 1981-03-03 | University Of Miami | Anti-fouling marine paints containing microencapsulated anti-fouling agents and the process of microencapsulation |
JPS5799507A (en) * | 1980-12-13 | 1982-06-21 | Katayama Chem Works Co Ltd | Industrial bactericidal and bacteriostatic composition |
US4561981A (en) * | 1984-01-27 | 1985-12-31 | Characklis William G | Treatment of fouling with microcapsules |
US4954338A (en) * | 1987-08-05 | 1990-09-04 | Rohm And Haas Company | Microbicidal microemulsion |
EP0338439B1 (en) * | 1988-04-18 | 1992-12-02 | Katayama Chemical, Inc. | A microbicidal/microbistatic composition |
FR2638101B1 (fr) * | 1988-10-21 | 1991-09-06 | Biocom Sa | Dispositif de filtration parallele d'une pluralite d'echantillons avec controle automatique des volumes filtres et du colmatage ainsi qu'avec indexation du filtre, et procede de filtration |
US5080831A (en) * | 1989-06-29 | 1992-01-14 | Buckeye International, Inc. | Aqueous cleaner/degreaser compositions |
US5547939A (en) * | 1991-06-14 | 1996-08-20 | The Regents Of The University Of California | Broad spectrum antimicrobial compounds and methods of use |
US5164096A (en) * | 1991-11-01 | 1992-11-17 | Nalco Chemical Company | Biocide microencapsulation |
US5444078A (en) * | 1993-10-01 | 1995-08-22 | Rohm And Haas Company | Fully water-dilutable microemulsions |
DE4340665A1 (de) * | 1993-11-30 | 1995-06-01 | Stockhausen Chem Fab Gmbh | Öl-in-Wasser-Emulsionen als Ersatz für Mikrobizide (Biozide) in wasserführenden Systemen |
DE4343857A1 (de) * | 1993-12-22 | 1995-06-29 | Hoechst Ag | Öl-in-Wasser-Emulsionen |
CN1069162C (zh) * | 1994-05-02 | 2001-08-08 | 诺尔科化学公司 | 用作改进的抗微生物剂的荧光杀生物剂组合物 |
US5536305A (en) * | 1994-06-08 | 1996-07-16 | Yu; Bing | Low leaching compositions for wood |
US5585341A (en) * | 1995-02-27 | 1996-12-17 | Buckeye International, Inc. | Cleaner/degreaser concentrate compositions |
US5632904A (en) * | 1995-04-06 | 1997-05-27 | Mainstream Engineering Corporation | Water disinfection method using metal-ligand complexes |
-
1998
- 1998-09-11 US US09/151,637 patent/US6096225A/en not_active Expired - Fee Related
-
1999
- 1999-06-25 JP JP2000570107A patent/JP2002524257A/ja active Pending
- 1999-06-25 WO PCT/US1999/014468 patent/WO2000015562A1/en not_active Application Discontinuation
- 1999-06-25 AU AU48340/99A patent/AU4834099A/en not_active Abandoned
- 1999-06-25 KR KR1020017003136A patent/KR20010073148A/ko not_active Application Discontinuation
- 1999-06-25 EP EP99931931A patent/EP1113995A4/en not_active Withdrawn
- 1999-06-25 NZ NZ510364A patent/NZ510364A/xx unknown
- 1999-06-25 BR BR9913586-8A patent/BR9913586A/pt not_active Application Discontinuation
- 1999-06-25 CA CA002342242A patent/CA2342242A1/en not_active Abandoned
- 1999-06-25 ZA ZA200101939A patent/ZA200101939B/en unknown
- 1999-06-25 CN CN99810796A patent/CN1316979A/zh active Pending
- 1999-06-25 ID IDW20010570A patent/ID28347A/id unknown
- 1999-07-28 TW TW088112776A patent/TW533190B/zh active
- 1999-09-07 AR ARP990104488A patent/AR021218A1/es unknown
- 1999-09-07 CO CO99056426A patent/CO5221043A1/es not_active Application Discontinuation
-
2001
- 2001-03-09 NO NO20011225A patent/NO20011225L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JP2002524257A (ja) | 2002-08-06 |
NO20011225D0 (no) | 2001-03-09 |
CA2342242A1 (en) | 2000-03-23 |
CN1316979A (zh) | 2001-10-10 |
ID28347A (id) | 2001-05-17 |
US6096225A (en) | 2000-08-01 |
KR20010073148A (ko) | 2001-07-31 |
AU4834099A (en) | 2000-04-03 |
CO5221043A1 (es) | 2002-11-28 |
BR9913586A (pt) | 2001-06-05 |
NZ510364A (en) | 2002-09-27 |
EP1113995A4 (en) | 2001-12-12 |
NO20011225L (no) | 2001-04-24 |
TW533190B (en) | 2003-05-21 |
WO2000015562A1 (en) | 2000-03-23 |
AR021218A1 (es) | 2002-07-03 |
EP1113995A1 (en) | 2001-07-11 |
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