JP5294625B2 - 置換化アミノシロキサンから由来するポリマー状反応生成物 - Google Patents
置換化アミノシロキサンから由来するポリマー状反応生成物 Download PDFInfo
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- JP5294625B2 JP5294625B2 JP2007506167A JP2007506167A JP5294625B2 JP 5294625 B2 JP5294625 B2 JP 5294625B2 JP 2007506167 A JP2007506167 A JP 2007506167A JP 2007506167 A JP2007506167 A JP 2007506167A JP 5294625 B2 JP5294625 B2 JP 5294625B2
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- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
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- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/442—Block-or graft-polymers containing polysiloxane sequences containing vinyl polymer sequences
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- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C09D183/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
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- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/10—Block or graft copolymers containing polysiloxane sequences
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- C14C9/00—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
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- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
- D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
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- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/356—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms
- D06M15/3568—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms containing silicon
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- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/65—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing epoxy groups
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Description
i.オレフィン性不飽和基によって置換されたアミノ基を含むアミノシロキサン;
ii.オレフィン性不飽和カルボン酸のフルオロ置換化アルキルエステル;及び任意に
iii.一つ以上のエチレン性不飽和コモノマー
の反応生成物を含む組成物を提供する。
R−(NH−A’)q−NH−A−
[式中、A及びA’はそれぞれ独立に、1から6の炭素原子を有する直鎖状または分枝状アルキレン基であり;q=0−4であり;Rは水素、1から4の炭素原子を有するアルキル基若しくはヒドロキシアルキル基、またはアルキル部分に1から4の炭素原子を有するアルコキシアルキル基若しくはカルボキシアルキル基である]。Rがカルボキシアルキル基である場合、それは好ましくはエステル化されている。より好ましくはq=0または1であり;A及びA’(存在すれば)はそれぞれ2から4の炭素原子を含む。
R-(NH-A')q-NH-A-Si(CH3)2-O-(Si(CH3)2-O)x-Si(CH3)2-A-NH-(A'-NH)q-R
[式中、A、A’、R、及びqは上述の通りであり、xは例えば4-1000であり、または下式を有して良い:。
R−(NH−A’)q−NH−A−
更には下式を有することができる:
R-(NH-A')q-NH-A-Si(CH3)2-O-(Si(CH3)2-O)x-Si(CH3)2-A-NH-(A'-NH)q-R、
CF3(CF2)7(CH2)2OCOCH=CH2
CF3(CF2)7(CH2)10OCOCH=CH2
CF3(CF2)6CH2OCOCH=CH2
CF3(CF2)8CH2OCOCH=CH2
(CF3)2CF(CF2)6(CH2)2OCOCH=CH2
(CF3)2CF(CF2)8(CH2)2OCOCH=CH2
(CF3)2CF(CF2)10(CH2)2OCOCH=CH2
CF3(CF2)9(CH2)2OCOCH=CH2
CF3(CF2)11(CH2)2OCOCH=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOCH=CH2
CF3(CF2)7SO2N(C2H5)(CH2)2OCOCH=CH2
(CF3)2CF(CF2)6CH2CH(OH)CH2OCOCH=CH2
C8F17−O−Ph−CH2OCOCH=CH2[Pfは1,4-フェニレンを表す]
(CF3)2CFOCOCH=CH2
(CF3)2CF(CH2)2OCOCH=CH2
−NH(R)CH2CHR”−COO−X−OOC−CR”=CH2
CF3(CF2)7(CH2)2OCOCH=CH2
CF3(CF2)7(CH2)2OCOC(CH3)=CH2
CF3(CF2)7(CH2)10OCOCH=CH2
CF3(CF2)7(CH2)10OCOC(CH3)=CH2
CF3(CF2)6CH2OCOCH=CH2
CF3(CF2)8CH2OCOCH=CH2
(CF3)2CF(CF2)6(CH2)2OCOCH=CH2
(CF3)2CF(CF2)8(CH2)2OCOCH=CH2
(CF3)2CF(CF2)10(CH2)2OCOCH=CH2
(CF3)2CF(CF2)6(CH2)2OCOC(CH3)=CH2
(CF3)2CF(CF2)8(CH2)2OCOC(CH3)=CH2
(CF3)2CF(CF2)10(CH2)2OCOC(CH3)=CH2
CF3(CF2)9(CH2)2OCOCH=CH2
CF3(CF2)9(CH2)2OCOC(CH3)=CH2
CF3(CF2)11(CH2)2OCOCH=CH2
CF3(CF2)11(CH2)2OCOC(CH3)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOCH=CH2
CF3(CF2)7SO2N(C2H5)(CH2)2OCOCH=CH2
(CF3)2CF(CF2)8CH2CH(OCOCH3)CH2OCOC(CH3)=CH2
(CF3)2CF(CF2)6CH2CH(OH)CH2OCOCH=CH2
C8F17−O−Ph−CH2OCOCH=CH2[Pfは1,4-フェニレンを表す]
C5F11−O−Ph−CH2OCOC(CH3)=CH2
C8F17−O−Ph−COOCH2CH(OH)CH2OCOC(CH3)=CH2
(CF3)2CFOCOC(CH3)=CH2
(CF3)2CF(CH2)2OCOC(CH3)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOC(F)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOC(Cl)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOC(Br)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOC(I)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOC(CF3)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOC(CN)=CH2
CF3(CF2)7SO2N(CH3)(CH2)2OCOC(C6H5)=CH2
CF3(CF2)7(CH2)2OCOC(F)=CH2
CF3(CF2)7(CH2)2OCOC(Cl)=CH2
CF3(CF2)7(CH2)2OCOC(Br)=CH2
CF3(CF2)7(CH2)2OCOC(I)=CH2
CF3(CF2)7(CH2)2OCOC(CF3)=CH2
CF3(CF2)7(CH2)2OCOC(CN)=CH2
CF3(CF2)7(CH2)2OCOC(C6H5)=CH2
アミノプロピル末端ブロック化ポリジメチルシロキサン(重合度(dp)250、30.4g)、ヘキサンジオールジアクリレート(1.22g)、キシレン(50.3g)、及びブタン−1−オール(50.6g)を反応容器にチャージし、窒素下で20分間90℃に加熱した。
1200cPの粘度と、0.38%w/wの窒素含量を有する下式のアミノ官能性シロキサン(40.5g)[II]、ステアリルアクリレート(5.2g)、キシレン(50.3g)、及びブタン−1−オール(50.7g)を反応容器にチャージし、窒素下で15分間90℃に加熱した。次いで反応容器にヘキサンジオールジアクリレート(1.53g)を加え、反応を窒素下で更に15分間90℃に保持した。
2500cPの粘度と、0.4%w/wの窒素含量を有する下式のアミノ官能性シロキサン(40.2g)[III]、ステアリルアクリレート(5.18g)、キシレン(51.6g)、及びブタン−1−オール(53.5g)を反応容器にチャージし、窒素下で15分間90℃に加熱した。次いで反応容器にヘキサンジオールジアクリレート(1.55g)を加え、反応を窒素下で更に15分間90℃に保持した。
次いで、フルオロモノマーCH2=CHCOO(CH2)2C8F17FA(30.2g)、ヒドロキシエチルメタクリレート(16.1g)、ドデカンチオール(1.05g)、2−ブタノン(32.8g)、及び1,1'−アゾ−ビス−シクロヘキサンカルボニトリル(0.45g)を反応容器に加え、反応温度を7時間90℃で維持し、撥水性且つ撥油性のフルオロカーボン参照ポリマーを得た。
処理された繊維の撥油性を、AATCC試験法118−1997を使用して評価した。
Claims (9)
- i.式−CH2CHR”−COO−X−OOC−CR”=CH2[式中、各R”は独立にHまたはメチルを表し、Xは1から20の炭素原子を有するアルキレン基を表す]の基によって置換されたアミノ基を含むアミノシロキサン;
ii.エチレン性不飽和カルボン酸のフルオロ置換化アルキルエステル;及び任意に
iii.一つ以上のエチレン性不飽和コモノマー
のポリマー状反応生成物を含む組成物。 - 前記アミノシロキサンが更に、エチレン性不飽和を有さない有機部分によって置換される、請求項1に記載の組成物。
- 前記アミノシロキサンのアミノ基のいくつかが、ケイ素に結合した式R−(NH−A’)q−NH−A−[式中、A及びA’はそれぞれ独立に、1から6の炭素原子を有する直鎖状または分枝状アルキレン基であり;q=0−4であり;Rは水素、1から4の炭素原子を有するアルキル基若しくはヒドロキシアルキル基である]の非置換アミノアルキル基である、請求項1に記載の組成物。
- 前記アミノシロキサンが、末端またはペンダント状アミノアルキル基を有するポリオルガノシロキサンである、請求項1から3のいずれか一項に記載の組成物。
- 前記アミノシロキサンが更に、ラクトン、エポキシド、イソシアネート、または無水物との反応によって修飾されたアミノ基を含む、請求項1から4のいずれか一項に記載の組成物。
- 前記フルオロ置換化アルキルエステルモノマーが、式CH2=C(Y)COO−D−Rf[式中、Rfは1から21の炭素原子を有するフルオロアルキル基であり、YはHまたはMeであり、Dは1から20の炭素原子を有する直鎖状または分枝状アルキレン基である]のエチレン性不飽和カルボン酸のフルオロ置換化アルキルエステルである、請求項1から5のいずれか一項に記載の組成物。
- 前記反応生成物が、0.1から95重量%の前記アミノシロキサン、5から95重量%の前記フルオロ置換化アルキルエステル、及び0から70重量%のコモノマーを含む、請求項1から6のいずれか一項に記載の組成物。
- 請求項1から7のいずれか一項に記載の組成物を含む織物処理組成物。
- 請求項1から8のいずれか一項に記載の組成物を、繊維、レザー、または紙に塗布することを特徴とする、繊維、レザー、カーペット、不織布、または紙を疎油性とする方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0407433.2A GB0407433D0 (en) | 2004-04-01 | 2004-04-01 | Substituted aminosiloxanes and polymeric products |
GB0407433.2 | 2004-04-01 | ||
PCT/US2005/004477 WO2005103156A2 (en) | 2004-04-01 | 2005-02-14 | Polymeric reaction products from substituted adminosiloxanes |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2007530766A JP2007530766A (ja) | 2007-11-01 |
JP5294625B2 true JP5294625B2 (ja) | 2013-09-18 |
Family
ID=32247688
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2007506167A Expired - Fee Related JP5294625B2 (ja) | 2004-04-01 | 2005-02-14 | 置換化アミノシロキサンから由来するポリマー状反応生成物 |
Country Status (8)
Country | Link |
---|---|
US (1) | US7642326B2 (ja) |
EP (1) | EP1735359B1 (ja) |
JP (1) | JP5294625B2 (ja) |
CN (1) | CN100497419C (ja) |
AT (1) | ATE409199T1 (ja) |
DE (1) | DE602005009938D1 (ja) |
GB (1) | GB0407433D0 (ja) |
WO (1) | WO2005103156A2 (ja) |
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GB0327067D0 (en) | 2003-11-21 | 2003-12-24 | Dow Corning | Polymeric products useful as oil repellents |
US7097785B2 (en) | 2004-04-12 | 2006-08-29 | Dow Corning Corporation | Fluoropolymer—amino terminated polydiorganosiloxane compositions for textile treatments |
CN101679779B (zh) * | 2007-04-25 | 2013-07-10 | 巴斯夫欧洲公司 | 带有生物钝性涂层的基底 |
DE102008002145A1 (de) * | 2008-06-02 | 2009-12-03 | Symrise Gmbh & Co. Kg | Kapsel mit organisch-anorganischer Hybridwand |
CN101906212B (zh) * | 2009-06-05 | 2012-05-09 | 中国中化股份有限公司 | 一种有机硅嵌段共聚物 |
CN105622943B (zh) * | 2016-03-24 | 2018-06-05 | 山东大学 | 一种同时含腈基和乙烯基的高分子量聚硅氧烷的合成及加成型热硫化腈硅橡胶的制备方法 |
CN105601845B (zh) * | 2016-03-24 | 2018-09-21 | 山东大学 | 一种高分子量含腈基聚硅氧烷的合成及过氧化物型热硫化腈硅橡胶的制备方法 |
JP7168693B2 (ja) * | 2018-07-12 | 2022-11-09 | ダウ グローバル テクノロジーズ エルエルシー | 水性ポリマー分散液およびそれを作製するプロセス |
CN110760047B (zh) * | 2018-07-26 | 2022-04-19 | 万华化学集团股份有限公司 | 一种含有硅氧烷基团的双仲胺及其制备方法和应用 |
CN111334177A (zh) * | 2020-04-24 | 2020-06-26 | 杨建伟 | 一种石墨烯改性聚氨酯超疏水防腐材料及其制法 |
CN112608703B (zh) * | 2020-11-25 | 2022-07-12 | 广州市白云化工实业有限公司 | 防污型硅烷改性聚醚胶及其制备方法 |
CN112961339A (zh) * | 2021-04-17 | 2021-06-15 | 郑州大学 | 一种新型硅烷封端聚醚及其合成方法 |
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US4070152A (en) * | 1976-01-12 | 1978-01-24 | Ciba-Geigy Corporation | Textile treating compositions for increasing water and oil repellency of textiles |
JPS60190408A (ja) * | 1984-03-12 | 1985-09-27 | Shin Etsu Chem Co Ltd | 撥水撥油性組成物 |
JPH0627196B2 (ja) * | 1984-03-12 | 1994-04-13 | 大日本印刷株式会社 | 放射線硬化性有機珪素化合物の製造法 |
US4617057A (en) * | 1985-06-04 | 1986-10-14 | Dow Corning Corporation | Oil and water repellent coating compositions |
US4697026A (en) * | 1986-01-06 | 1987-09-29 | Dow Corning Corporation | Acryl functional silicone compounds |
US5068295A (en) | 1989-02-15 | 1991-11-26 | Dainichiseika Color & Chemicals Mfg. Co., Ltd. | Water and oil repellants |
DE4201604A1 (de) | 1992-01-22 | 1993-07-29 | Bayer Ag | Fluorhaltige copolymerisate und daraus hergestellte waessrige dispersionen |
JPH078909A (ja) * | 1993-06-28 | 1995-01-13 | Olympus Optical Co Ltd | 超音波振動子の駆動装置 |
DE69306578T2 (de) | 1993-10-19 | 1997-04-10 | Minnesota Mining & Mfg | Hochleistungszusammensetzungen mit wasser- und ölabweisenden Eigenschaften |
JPH08109580A (ja) * | 1994-10-05 | 1996-04-30 | Shin Etsu Chem Co Ltd | 繊維処理用組成物 |
JP3211656B2 (ja) | 1996-03-18 | 2001-09-25 | 信越化学工業株式会社 | 水溶性繊維処理剤及びその製造方法 |
US5739192A (en) * | 1996-11-20 | 1998-04-14 | Dow Corning Corporation | Polysiloxane copolymers from Michael Adduct reactions |
JPH10251598A (ja) * | 1997-03-17 | 1998-09-22 | Toyo Ink Mfg Co Ltd | 硬化性樹脂組成物 |
JP4066497B2 (ja) * | 1998-03-23 | 2008-03-26 | ダイキン工業株式会社 | 含フッ素共重合体を含んでなる化粧品 |
DE19952323A1 (de) * | 1999-10-29 | 2001-05-03 | Few Chemicals Gmbh Wolfen | Schutzschicht mit antiadhäsiven Eigenschaften |
JP4231983B2 (ja) | 2000-12-22 | 2009-03-04 | 信越化学工業株式会社 | 水溶性撥水撥油処理剤及びその製造方法 |
JP2002266245A (ja) | 2001-03-13 | 2002-09-18 | Daikin Ind Ltd | 繊維製品の撥水撥油処理 |
GB0120058D0 (en) | 2001-08-17 | 2001-10-10 | Dow Corning | Polysiloxanes and their preparation |
JP2006188546A (ja) | 2003-02-10 | 2006-07-20 | Daikin Ind Ltd | 仕上げ加工用水性分散液 |
JP2006188545A (ja) | 2003-02-10 | 2006-07-20 | Daikin Ind Ltd | 撥水撥油剤水性分散液組成物 |
GB0327067D0 (en) * | 2003-11-21 | 2003-12-24 | Dow Corning | Polymeric products useful as oil repellents |
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2004
- 2004-04-01 GB GBGB0407433.2A patent/GB0407433D0/en not_active Ceased
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2005
- 2005-02-14 JP JP2007506167A patent/JP5294625B2/ja not_active Expired - Fee Related
- 2005-02-14 DE DE602005009938T patent/DE602005009938D1/de not_active Expired - Fee Related
- 2005-02-14 EP EP05713422A patent/EP1735359B1/en not_active Not-in-force
- 2005-02-14 CN CNB2005800096427A patent/CN100497419C/zh not_active Expired - Fee Related
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US7642326B2 (en) | 2010-01-05 |
DE602005009938D1 (de) | 2008-11-06 |
ATE409199T1 (de) | 2008-10-15 |
US20070208152A1 (en) | 2007-09-06 |
EP1735359A2 (en) | 2006-12-27 |
GB0407433D0 (en) | 2004-05-05 |
WO2005103156A3 (en) | 2006-03-02 |
EP1735359B1 (en) | 2008-09-24 |
WO2005103156A2 (en) | 2005-11-03 |
JP2007530766A (ja) | 2007-11-01 |
CN1938350A (zh) | 2007-03-28 |
CN100497419C (zh) | 2009-06-10 |
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