Aqueous dispersion with fungicidal and algicidal action 机翻标题: 暂无翻译,请尝试点击翻译按钮。

源语言标题
(JP2010235627) 殺菌​作用​および​殺​藻​作用​を​有する​水性​分散​液
公开号/公开日
JP2010235627 A 2010-10-21 [JP2010235627] / 2010-10-21
申请号/申请日
2010JP-0145544 / 2010-06-25
发明人
BEILFUSS WOLFGANG;GRADTKE RALF;MANGOLD HERBERT;KASSENS ELKE;WEBER KLAUS;
申请人
AIR LIQUIDE SANTE;
主分类号
IPC分类号
A01N-025/04A01N-025/22A01N-025/30A01N-043/64A01N-043/70A01N-043/80A01N-047/18A01P-003/00A01P-013/00B01F-017/00
摘要
(JP2010235627) PROBLEM TO BE SOLVED: To provide a stable preservative with algicidal and fungicidal actions in a form of a dispersion.  SOLUTION: The preservative comprises: (a) at least one algicidal triazine; (b) at least one fungicidal isothiazolone; and (c) at least one dispersion stabilizer selected from the group consisting of (c1) sulfite salts, hydrogen sulfite salts, a compound which releases sulfite and a compound which releases hydrogen sulfite, and (c2) hypophosphite salts and a compound which releases hypophosphite salt.  COPYRIGHT: (C)2011,JPO&INPIT
机翻摘要
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地址
代理人
代理机构
;
优先权号
2002DE-1037264 2002-08-14
主权利要求
(JP2010235627) 1. In the form of a dispersion having a bactericidal action algicidal or a preservative, a) at least one algicidal triazine compound having a 1, b) an isothiazolone germicidal properties of at least 1, and c) at least one dispersion stabilizer is 1, c1) sulfites, hydrogen sulfites, sulfites and hydrogen sulfites releasing compound which releases the compound of, and c2) hypophosphorous acid salts and hypophosphorous acid salts selected from the group consisting releasing compound including the dispersion stabilizer is a preservative.  2. D) at least one of an imidazole derivative such as 1, in particular, methyl benzimidazole -2 - ylcarbamate according to claim 1 characterized in further comprising a preservative.  3. Wherein the triazine compound, N2 , N4  -- 1, 3, 5 - triazine - 2, 4 - diamine diisopropyl -6 - methylthio, N2  -(tert--butyl) -N4  -- 1, 3, 5 - triazine - 2, 4 - diamine and -6 - methylthio ethyl N2  -(tert--butyl) -N4  --6 - cyclopropyl - 2, 4 - - 1, 3, 5 - triazine diamine selected from methylthio and preservative according to claim 2 or claim 1.  4. Wherein the isothiazolone, isothiazolin -3 - ON, N- Octylisothiazolone, Methyl isothiazoline N -, -N- Cidex Methylisothiazolone 5 -, 4, 5 - - dichloro -N- Octylisothiazolone, benzisothiazolone and Butyl benzisothiazolone N- according to any one of claims 1-3 characterized in that it is selected from the preservative.  5. Wherein the dispersion stabilizer, sulfur dioxide, aqueous sulfur dioxide, alkali metal sulfite, ammonium sulfite, bisulfite and bis (bis (2 - hydroxyethyl) ammonium), bis (triethylammonium) sulfite, bis ((2 - - hydroxyethyl) ammonium) sulfite, an alkaline earth metal salt of sulfurous acid, tri - (sodium bisulfite) Glyoxal bis, (sodium hydrogen sulphite) adduct Glutaraldehyde bis, lignosulfonic acid and a sulfite salt is selected from a waste liquid according to any one of claims 1-4 and preservatives.  6. Wherein the dispersion stabilizer, the alkali metal salt of sulfurous acid, in particular, characterized in that the potassium sulfite preservative according to claim 5.  7. Wherein the dispersion stabilizer, an alkali metal salt of hypophosphorous acid, ammonium hypophosphite, an alkali earth metal salt of hypophosphorous acid, hypophosphorous acid and hypophosphorous acid and zinc is selected from thiabendazole and antiseptic agent according to any one of claims 1-4.  8. B) a pair of isothiazolone in c) the molar ratio of the dispersion stabilizer, from 10:1 1:10, 1:2 and preferably from 2:1, 1:1.5 1. 1:1 1. 5:1 1:1.1 especially from as according to any one of claims 1-7 from and characterized in that the preservative.  9. A), b), c) and optionally d) the total content of, from 99 1% by weight, preferably from 60 5% by weight, in particular from 10 to 30 weight % preservative characterized according to any one of claims 1-8.  10. A) from 12 1% by weight, preferably from 9 3% by weight, more preferably 7 4% by weight of triazine from said compound according to any one of claims 1-9 preservative.  11. B) from 8 1% by weight, preferably from 6 2% by weight, more preferably from 5 3% by weight of isothiazolone according to any one of claims 1-10 and characterized in that it comprises a preservative.  12. C) from 5 0.5% by weight, preferably from 3 1% by weight, from 2.5 weight % and even more preferably of 1.5 and containing a dispersion stabilizer according to any one of claims 1-11 preservative.  13. D) from 13 weight % 2, 11 weight % and preferably from 4, 9 6% by weight and in particular from the imidazole derivative according to any one of claims 1-12 characterized in that it comprises a preservative.  14. 10 Weight % and less than, is less than 7 weight % and more preferably, less than 5 weight % in a solvent according to any one of claims 1-13 preservative.  15. 1 One or more functional additives according to any one of claims 1-14 characterized in further comprising a preservative.  16. Wherein the additive agent, nonionic surface active agent, a defoaming agent, zinc oxide, container preservatives, thickeners, starch, zinc pyrithione, a benzalkonium salt, 22 salt Badakku, Vantocil IB salts, thiabendazole, Dodecyl guanidinium acetate, butylcarbamic acid iodopropyl, Diuron, -2 - benzothiophene Cyclohexyl carboxamide, and the emulsifier and is selected from a preservative according to claim 15 wherein.  17. As an additive, 0 weight % of a nonionic surface active agent is from 2, 0.2 weight % of an antifoaming agent from 0, 20 0% by weight of zinc oxide of from, 0% by weight/0.2 from the 0 or 1 from the container weight % preservative and a thickener characterized in that the preservative according to claim 16.  18. Consisting essentially of, a) 5.6 weight % of N2  -(tert--butyl) -N4  -- 2, 4 - - 1, 3, 5 - -6 - methylthio ethyl triazine diamine, b) 4 weight % of Octylisothiazolone N -, c) 2 weight % of potassium metabisulfite, and d) 7.8 weight % of the water and the balance Carbendazime characterized as according to any one of claims 1-17 preservative.  19. Does not contain Carbendazime, consisting essentially of, a) 6 weight % of N2  -(tert--butyl) -N4  -- 1, 3, 5 - triazine - 2, 4 - diamine -6 - methylthio ethyl, b) 2 weight % of Octylisothiazolone N -, c) 1 weight % of potassium disulfite, d) 10 weight % of zinc oxide, e) 19 weight % of zinc, and f) 1 weight % of a nonionic surfactant and the balance comprising water and a preservative according to any one of claims 1-18.  20. For application to the internal or external in or on the industrial product for use in industrial products according to any one of claims 1-19 preservative in the aqueous dispersion in use.  21. Wherein said industrial product, a finish, paint, plaster, varnishes, fillers, sealants, plastics, composite materials, wood, concrete, stone, paper, board, leather, textiles, glues and adhesives material characterized in that it is selected from a use according to claim 20.  22. Wherein said industrial product, pH of 1 from 13, 12 or 3 is preferably present from, one or more of pH 11, pH 12 preferably greater than, in particular greater than 13 and is present at a pH of the use claims 20 or 21.  23. Wherein said industrial product, from 5 weight % 0.1, 3 weight % and preferably from 0.5, 2 1% by weight of the preservative from the particular used according to any one of claims 20-22 characterized in use.  24. A) at least one algicidal triazine-b and 1) at least one bactericidal composition comprising a 1 for the stabilization of isothiazolone of i) a sulfite, bisulfite, metabisulfite or bisulfite releasing compound releasing compound, or ii) hypophosphite salt to release the hypophosphite salt or use of the compounds.
法律状态
(JP2010235627) LEGAL DETAILS FOR JP2010235627  Actual or expected expiration date=2014-01-28    Legal state=DEAD    Status=REVOKED     Event publication date=2010-06-25  Event code=JP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=JP JP2010145544  Application date=2010-06-25  Standardized application number=2010JP-0145544     Event publication date=2010-10-21  Event code=JP/A  Event indicator=Pos  Event type=Examination events  Published application  Publication country=JP  Publication number=JP2010235627  Publication stage Code=A  Publication date=2010-10-21  Standardized publication number=JP2010235627     Event publication date=2012-11-14  Event code=JP/A131  Event indicator=Neg  Event type=Examination events  Notification of reasons for refusal  Effective date of the event=2012-11-13  JAPANESE INTERMEDIATE CODE: A132     Event publication date=2013-02-08  Event code=JP/A601  Event type=Examination events  Written request for extension of term  Effective date of the event=2013-02-07  JAPANESE INTERMEDIATE CODE: A601     Event publication date=2013-02-14  Event code=JP/A602  Event type=Examination events  Written permission of extension of term  Effective date of the event=2013-02-13  JAPANESE INTERMEDIATE CODE: A602     Event publication date=2013-05-11  Event code=JP/A521  Event type=Restitution or restoration  Written amendment  Effective date of the event=2013-05-10  JAPANESE INTERMEDIATE CODE: A523     Event publication date=2013-09-11  Event code=JP/A01  Event indicator=Pos  Event type=Event indicating In Force  Written decision to grant a patent or to grant a registration (utility model)  Effective date of the event=2013-09-10  JAPANESE INTERMEDIATE CODE: A01     Event publication date=2014-01-29  Event code=JP/A045  Event indicator=Neg  Event type=Event indicating Not In Force  Written measure of dismissal of application  Effective date of the event=2014-01-28  JAPANESE INTERMEDIATE CODE: A045
专利类型码
A
国别省市代码
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