RU2009110161A - Пленкообразующая композиция со способностью к растеканию - Google Patents
Пленкообразующая композиция со способностью к растеканию Download PDFInfo
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- RU2009110161A RU2009110161A RU2009110161/21A RU2009110161A RU2009110161A RU 2009110161 A RU2009110161 A RU 2009110161A RU 2009110161/21 A RU2009110161/21 A RU 2009110161/21A RU 2009110161 A RU2009110161 A RU 2009110161A RU 2009110161 A RU2009110161 A RU 2009110161A
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- hydrocarbon radicals
- monovalent hydrocarbon
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- 239000000203 mixture Substances 0.000 title claims abstract 29
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract 10
- 229930195733 hydrocarbon Natural products 0.000 claims abstract 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 4
- 125000002947 alkylene group Chemical group 0.000 claims abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract 2
- 229920001281 polyalkylene Polymers 0.000 claims abstract 2
- 229920001296 polysiloxane Polymers 0.000 claims abstract 2
- ZQTYRTSKQFQYPQ-UHFFFAOYSA-N trisiloxane Chemical class [SiH3]O[SiH2]O[SiH3] ZQTYRTSKQFQYPQ-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 9
- 229910004298 SiO 2 Inorganic materials 0.000 claims 4
- -1 alkyl phosphate esters Chemical class 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000000839 emulsion Substances 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910004283 SiO 4 Inorganic materials 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims 1
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 150000008051 alkyl sulfates Chemical class 0.000 claims 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims 1
- 150000008052 alkyl sulfonates Chemical class 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 150000003014 phosphoric acid esters Chemical class 0.000 claims 1
- 239000002685 polymerization catalyst Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000010420 shell particle Substances 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 229910020489 SiO3 Inorganic materials 0.000 abstract 2
- 229910052681 coesite Inorganic materials 0.000 abstract 2
- 229910052906 cristobalite Inorganic materials 0.000 abstract 2
- 235000012239 silicon dioxide Nutrition 0.000 abstract 2
- 239000000377 silicon dioxide Substances 0.000 abstract 2
- 229910052682 stishovite Inorganic materials 0.000 abstract 2
- 229910052905 tridymite Inorganic materials 0.000 abstract 2
- 229940075614 colloidal silicon dioxide Drugs 0.000 abstract 1
- 229910052909 inorganic silicate Inorganic materials 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
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- 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
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- A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
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Abstract
1. Композиция, содержащая: ! a) Частицы с сердцевиной из коллоидного диоксида кремния/силиконовой оболочкой, содержащие (i) от приблизительно 90 мас.% до приблизительно 10 мас.% сердцевин из коллоидного диоксида кремния и (ii) от приблизительно 10 мас.% до приблизительно 90 мас.% оболочек из полиорганосилоксана формулы ! MaDbTcQd, ! в которой ! Ma = (Rl)(R2)(R3)SiO2/2; ! Db = (R4)(R5)SiO2/2; ! Tc = (R6)SiO3/2; ! Qd выбран из группы, состоящей из (OH)SiO3/2 или SiO4/2, ! где каждый из R1, R2, R3, R4, R5 и R6 независимо выбран из группы, состоящей из OH, линейных или разветвленных одновалентных углеводородных радикалов из от 1 до 30 атомов углерода, одновалентного арилалкила, арильных циклических углеводородных радикалов, где отношения M к D к T к Q соответствуют следующим соотношениям: ! 0<(a/d)<2; ! 0,1<(b/d)<10; ! 0<(c/d)<10; ! b) модифицированный полиалкиленоксидом трисилоксан формулы: ! M1 eD1 fD2 gM2 h, ! в которой ! M1 e = R7R8R9SiO1/2; ! M2 h= R10R11R12SiO1/2; ! D1 f= R13R14SiO2/2; ! D2 g= R15R16SiO2/2; ! где каждый из R7, R10 и R15 независимо выбран из группы, состоящей из от 1 до 4 одновалентных углеводородных радикалов или R17; ! и они удовлетворяют соотношению, состоящему в том, что когда g = 0, тогда как R7, так и R10, представляют собой R17, когда g не равен нулю, тогда каждый из R7 и R10 независимо выбран из группы, состоящей из от 1 до 4 одновалентных углеводородных радикалов; ! R15 представляет собой R17; ! R8, R9, R11, R12, R13, R14 и R16 независимо выбраны из группы, состоящей из от 1 до 4 одновалентных углеводородных радикалов; ! где подстрочные знаки e, f, g и h представляют собой ноль или 1 и удовлетворяют следующему соотношению: ! e + f+ g + h = 3, ! при условии, что когда g представляет собой 0, тогда R7 или R10 представляют собой R17; ! R17 представляет собой алкиленоксидную гр
Claims (21)
1. Композиция, содержащая:
a) Частицы с сердцевиной из коллоидного диоксида кремния/силиконовой оболочкой, содержащие (i) от приблизительно 90 мас.% до приблизительно 10 мас.% сердцевин из коллоидного диоксида кремния и (ii) от приблизительно 10 мас.% до приблизительно 90 мас.% оболочек из полиорганосилоксана формулы
MaDbTcQd,
в которой
Ma = (Rl)(R2)(R3)SiO2/2;
Db = (R4)(R5)SiO2/2;
Tc = (R6)SiO3/2;
Qd выбран из группы, состоящей из (OH)SiO3/2 или SiO4/2,
где каждый из R1, R2, R3, R4, R5 и R6 независимо выбран из группы, состоящей из OH, линейных или разветвленных одновалентных углеводородных радикалов из от 1 до 30 атомов углерода, одновалентного арилалкила, арильных циклических углеводородных радикалов, где отношения M к D к T к Q соответствуют следующим соотношениям:
0<(a/d)<2;
0,1<(b/d)<10;
0<(c/d)<10;
b) модифицированный полиалкиленоксидом трисилоксан формулы:
M1 eD1 fD2 gM2 h,
в которой
M1 e = R7R8R9SiO1/2;
M2 h= R10R11R12SiO1/2;
D1 f= R13R14SiO2/2;
D2 g= R15R16SiO2/2;
где каждый из R7, R10 и R15 независимо выбран из группы, состоящей из от 1 до 4 одновалентных углеводородных радикалов или R17;
и они удовлетворяют соотношению, состоящему в том, что когда g = 0, тогда как R7, так и R10, представляют собой R17, когда g не равен нулю, тогда каждый из R7 и R10 независимо выбран из группы, состоящей из от 1 до 4 одновалентных углеводородных радикалов;
R15 представляет собой R17;
R8, R9, R11, R12, R13, R14 и R16 независимо выбраны из группы, состоящей из от 1 до 4 одновалентных углеводородных радикалов;
где подстрочные знаки e, f, g и h представляют собой ноль или 1 и удовлетворяют следующему соотношению:
e + f+ g + h = 3,
при условии, что когда g представляет собой 0, тогда R7 или R10 представляют собой R17;
R17 представляет собой алкиленоксидную группу формулы:
R18O(C2H4O)j(C3H6O)k(C4H8O)mR19,
где R18 представляет собой линейный или разветвленный углеводородный радикал, имеющий от 2 до 6 атомов углерода,
R19 выбран из группы, состоящей из H, ацетила или одновалентного углеводородного радикала из от 1 до 6 атомов углерода и подстрочные знаки j, k и m представляют собой ноль или положительное целое число и удовлетворяют ограничению 4 <j + k + m ≤ 20;
c) эмульгатор, содержащий анионное поверхностно-активное вещество, выбранное из группы, состоящей из алкиларилсульфонатов, алкилсульфонатов, алкилсульфатов и сульфатов алкильных простых эфиров, алкильных фосфатных сложных эфиров, алкиларильных фосфатных сложных эфиров, спиртовых алкоксилатных фосфатных сложных эфиров и алкиларилалкоксилатных фосфатных сложных эфиров и их смесей; и
d) соль кислого катализатора полимеризации.
2. Композиция по п.1, в которой R7 представляет собой метил.
3. Композиция по п.1, в которой R8 представляет собой метил.
4. Композиция по п.1, в которой R9 представляет собой метил.
5. Композиция по п.1, в которой R10 представляет собой метил.
6. Композиция по п.1, в которой R11 представляет собой метил.
7. Композиция по п.1, в которой R12 представляет собой метил.
8. Композиция по п.1, в которой подстрочный знак k представляет собой 2 или 3.
9. Композиция по п.1, в которой x равен нулю.
10. Композиция по п.1, в которой y равен единице.
11. Композиция по п.1, в которой R18 варьирует от 3 до 4.
12. Композиция по п.1, в которой R19 представляет собой метил или водород.
13. Композиция по п.1, в которой R17 представляет собой CH2CH2CH2-O-(CH2CH2-O)8-H или CH2CH(CH3)CH2-O-(CH2-CH(CH3)-O)12-CH3.
14. Композиция по п.1, в которой R7, R8, R9, R10, R11 и R12 представляют собой метил, подстрочный знак k составляет 2 или 3, x равен нулю, y равен единице, R18 варьирует от 3 до 4, R19 представляет собой метил или водород, и R17 представляет собой CH2CH2CH2-O-(CH2CH2-O)8-H или CH2CH(CH3)CH2-O-(CH2-CH(CH3)-O)12-CH3.
15. Эмульсия, содержащая композицию по п.1, в которой композиция по п.1 представлена в дисперсной фазе.
16. Эмульсия, содержащая композицию по п.1, в которой композиция по п.1 представлена в непрерывной фазе.
17. Пленка, содержащая композицию по п.1.
18. Пленка, содержащая композицию по п.14.
19. Косметическая композиция, содержащая композицию по п.1.
20. Сельскохозяйственная композиция, содержащая композицию по п.1.
21. Композиция для ухода за домом, содержащая композицию по п.1.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82310506P | 2006-08-22 | 2006-08-22 | |
| US60/823,105 | 2006-08-22 | ||
| US11/840,304 | 2007-08-17 | ||
| US11/840,304 US7851581B2 (en) | 2006-08-22 | 2007-08-17 | Film forming composition with spreading properties |
| PCT/US2007/018399 WO2008024308A2 (en) | 2006-08-22 | 2007-08-20 | Film forming composition with spreading properties |
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| Publication Number | Publication Date |
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| RU2009110161A true RU2009110161A (ru) | 2010-09-27 |
| RU2517960C2 RU2517960C2 (ru) | 2014-06-10 |
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| RU2009110161/13A RU2517960C2 (ru) | 2006-08-22 | 2007-08-20 | Пленкообразующая композиция со способностью к растеканию |
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| Country | Link |
|---|---|
| US (1) | US7851581B2 (ru) |
| EP (1) | EP2088858A1 (ru) |
| CN (1) | CN101528031B (ru) |
| BR (1) | BRPI0716050A2 (ru) |
| MX (1) | MX2009001900A (ru) |
| RU (1) | RU2517960C2 (ru) |
| WO (1) | WO2008024308A2 (ru) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US7935842B2 (en) * | 2006-02-09 | 2011-05-03 | Momentive Performance Materials Inc. | Hydrolysis resistant organomodified trisiloxane surfactants |
| US7964032B2 (en) * | 2006-10-17 | 2011-06-21 | Momentive Performance Materials Inc. | Fluorine-free trisiloxane surfactant compositions for use in coatings and printing ink compositions |
| US7763178B2 (en) * | 2007-02-02 | 2010-07-27 | Smartpool, Inc. | Biodegradable surface layer film for pools or spas to prevent evaporation and heat loss |
| CN101657489B (zh) * | 2007-03-08 | 2013-07-17 | 莫门蒂夫性能材料股份有限公司 | 抗水解的有机改性三硅氧烷表面活性剂 |
| US7923507B2 (en) * | 2007-08-30 | 2011-04-12 | Siovation, Llc | Polyorganosiloxane—containing compositions |
| WO2009034933A1 (ja) * | 2007-09-14 | 2009-03-19 | Kao Corporation | 垂直磁気記録方式ハードディスク用基板用水系洗浄剤組成物 |
| EP2039747A1 (en) * | 2007-09-17 | 2009-03-25 | The Procter and Gamble Company | Process for treating hard surface |
| DE102008043185A1 (de) | 2008-10-27 | 2010-04-29 | Evonik Goldschmidt Gmbh | Nicht schäumende organische Tenside als Additive für Tankmischungszubereitungen im Pflanzenschutz |
| BR112012008808B8 (pt) * | 2009-11-06 | 2023-09-26 | Avon Prod Inc | Método para prevenir ou reduzir a aparência frisada do cabelo |
| US8932569B2 (en) | 2009-11-06 | 2015-01-13 | Avon Products, Inc. | Methods and compositions for preventing or reducing frizzy appearance of hair |
| ES2554941T3 (es) * | 2011-02-04 | 2015-12-28 | Basf Se | Composición que contiene un poliorganosiloxano, un larvicida y un disolvente orgánico |
| RS58071B1 (sr) * | 2011-11-17 | 2019-02-28 | Sano Brunos Entpr Ltd | Formulacija za čišćenje poda koja sadrži sredstvo za kontrolu insekata |
| US10577801B2 (en) * | 2016-07-15 | 2020-03-03 | Firestone Building Products Company, Llc | Silicone membranes |
| CR20190216A (es) | 2016-11-02 | 2019-11-07 | Paramount Products 1 Llc | Composiciones adyudantes para ´productos químicos para el tratamiento de plantas |
| US11666048B2 (en) | 2017-02-24 | 2023-06-06 | Corbet Scientific, Llc | Treatment for plants in conjunction with harvesting |
| US20190233327A1 (en) * | 2017-12-28 | 2019-08-01 | Guardian Glass, LLC | Anti-Corrosion Coating for a Glass Substrate |
| SG11202010011RA (en) | 2018-04-17 | 2020-11-27 | Celldex Therapeutics Inc | Anti-cd27 and anti-pd-l1 antibodies and bispecific constructs |
| CA3106834A1 (en) | 2018-07-20 | 2020-01-23 | Stepan Company | Reduced-residue hard surface cleaner and method for determining film/streak |
| WO2020179555A1 (ja) * | 2019-03-06 | 2020-09-10 | 扶桑化学工業株式会社 | コロイダルシリカ及びその製造方法 |
| CN112022027A (zh) * | 2020-08-26 | 2020-12-04 | 山东奥古生物科技有限公司 | 一种一次性洗碗巾及其制备方法 |
| CN116004328B (zh) * | 2022-12-27 | 2024-09-27 | 广东水卫仕生物科技有限公司 | 一种长效抑菌的地板清洁剂组合物及其制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US4902499A (en) * | 1986-04-04 | 1990-02-20 | The Procter & Gamble Company | Hair care compositions containing a rigid silicone polymer |
| JP2992591B2 (ja) * | 1989-12-18 | 1999-12-20 | ジーイー東芝シリコーン株式会社 | シリカコア―シリコーンシェル体、これを分散含有するエマルジョンおよびエマルジョンの製造方法 |
| WO1993021263A1 (fr) * | 1992-01-31 | 1993-10-28 | Vainerman Efim S | Materiau, polymere poreux et son procede d'obtention |
| NZ314275A (en) | 1996-02-21 | 1998-07-28 | Osi Specialties Inc | Foam-reducing surfactant matrix containing siloxane alkoxylate foam control agent and at least one organosilicone as surfactant |
| JPH10114622A (ja) | 1996-10-11 | 1998-05-06 | Toshiba Silicone Co Ltd | 化粧料組成物 |
| FR2767473B1 (fr) * | 1997-08-25 | 2000-03-10 | Oreal | Compositions cosmetiques contenant un copolymere bloc silicone polyoxyalkylene amine et un agent conditionneur et leurs utilisations |
| FR2792191B1 (fr) * | 1999-04-16 | 2004-04-30 | Oreal | Composition cosmetique comprenant l'association d'un ester particulier et d'un compose silicone |
| EP1380282B1 (en) | 2001-04-20 | 2005-11-30 | Ge Toshiba Silicones Co., Ltd. | Cosmetic hair preparation composition |
| AU2002256735A1 (en) | 2001-04-30 | 2002-11-11 | Unilever Plc | Hair treatment compositions |
| AU2002302570A1 (en) * | 2001-04-30 | 2002-11-11 | Unilever Plc | Hair treatment compositions |
| US20030044372A1 (en) | 2001-08-30 | 2003-03-06 | Legrow Gary E. | Stable aqueous emulsions of alkoxytrimethylsilane fluids |
| US8142767B2 (en) | 2003-12-05 | 2012-03-27 | Momentive Performance Materials Japan Llc | Cosmetic hair composition |
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- 2007-08-20 MX MX2009001900A patent/MX2009001900A/es active IP Right Grant
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- 2007-08-20 CN CN2007800393244A patent/CN101528031B/zh not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0716050A2 (pt) | 2013-09-24 |
| MX2009001900A (es) | 2009-03-06 |
| WO2008024308A3 (en) | 2008-04-24 |
| RU2517960C2 (ru) | 2014-06-10 |
| CN101528031A (zh) | 2009-09-09 |
| CN101528031B (zh) | 2013-08-14 |
| EP2088858A1 (en) | 2009-08-19 |
| US20080107696A1 (en) | 2008-05-08 |
| WO2008024308A2 (en) | 2008-02-28 |
| US7851581B2 (en) | 2010-12-14 |
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