JPH0366429B2 - - Google Patents
Info
- Publication number
- JPH0366429B2 JPH0366429B2 JP63045352A JP4535288A JPH0366429B2 JP H0366429 B2 JPH0366429 B2 JP H0366429B2 JP 63045352 A JP63045352 A JP 63045352A JP 4535288 A JP4535288 A JP 4535288A JP H0366429 B2 JPH0366429 B2 JP H0366429B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- groups
- formula
- weight
- organopolysiloxane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920001296 polysiloxane Polymers 0.000 claims description 32
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 16
- 239000000835 fiber Substances 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 15
- 125000003700 epoxy group Chemical group 0.000 claims description 15
- 239000004593 Epoxy Substances 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- 150000001282 organosilanes Chemical class 0.000 claims description 13
- 125000000962 organic group Chemical group 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 10
- 125000003277 amino group Chemical group 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 7
- -1 aminosiloxane Chemical class 0.000 description 19
- 150000002430 hydrocarbons Chemical class 0.000 description 17
- 239000012209 synthetic fiber Substances 0.000 description 16
- 229920002994 synthetic fiber Polymers 0.000 description 16
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 238000004383 yellowing Methods 0.000 description 10
- 229920000742 Cotton Polymers 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000005108 dry cleaning Methods 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 3
- 125000005375 organosiloxane group Chemical group 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229920002972 Acrylic fiber Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229950011008 tetrachloroethylene Drugs 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 241000237518 Arion Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- 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
- D06M15/37—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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- 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
- D06M15/37—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
- D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of 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; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
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Claims (1)
- ãç¹èš±è«æ±ã®ç¯å²ã ïŒ (A) äžè¬åŒ ãããã«R1ãR2ãR3ã¯åäžãŸãã¯ç°çš®ã®ççŽ
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100éééšã«å¯ŸããŠïŒã50éééšã®ãšããã·
åºå«æãªã«ã¬ãã·ã©ã³ã®å æ°Žå解瞮åç© ãšãããªãããšãç¹åŸŽãšããç¹ç¶åŠçå€ã
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63045352A JPH01221580A (ja) | 1988-02-27 | 1988-02-27 | ç¹ç¶åŠçå€ |
| KR1019890002267A KR930005939B1 (ko) | 1988-02-27 | 1989-02-25 | ì¬ì ì²ëŠ¬ì |
| US07/315,879 US5025076A (en) | 1988-02-27 | 1989-02-27 | Silicone-based fabric finishing agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63045352A JPH01221580A (ja) | 1988-02-27 | 1988-02-27 | ç¹ç¶åŠçå€ |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01221580A JPH01221580A (ja) | 1989-09-05 |
| JPH0366429B2 true JPH0366429B2 (ja) | 1991-10-17 |
Family
ID=12716884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63045352A Granted JPH01221580A (ja) | 1988-02-27 | 1988-02-27 | ç¹ç¶åŠçå€ |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US5025076A (ja) |
| JP (1) | JPH01221580A (ja) |
| KR (1) | KR930005939B1 (ja) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2935879B2 (ja) * | 1990-09-05 | 1999-08-16 | æ±ã¬ã»ããŠã³ãŒãã³ã°ã»ã·ãªã³ãŒã³æ ªåŒäŒç€Ÿ | ç¹ç¶åŠçå€çµæç© |
| DE4117864A1 (de) * | 1991-05-31 | 1992-12-03 | Pfersee Chem Fab | Waessrige dispersionen von polysiloxanen |
| JP2588804B2 (ja) * | 1991-08-30 | 1997-03-12 | æ±ã¬ã»ããŠã³ãŒãã³ã°ã»ã·ãªã³ãŒã³æ ªåŒäŒç€Ÿ | ããªãšã¹ãã«ç¹ç¶åŠçå€çµæç© |
| JP3224862B2 (ja) * | 1992-06-25 | 2001-11-05 | æ±ã¬ã»ããŠã³ãŒãã³ã°ã»ã·ãªã³ãŒã³æ ªåŒäŒç€Ÿ | ã¢ããåºå«æãªã«ã¬ãããªã·ãããµã³ããã³ãã®è£œé æ¹æ³ |
| DE4330967A1 (de) * | 1993-09-13 | 1995-03-16 | Pfersee Chem Fab | Organische Siliciumverbindungen enthaltende Zusammensetzungen fÃŒr die Behandlung von Fasermaterialien |
| JP3095330B2 (ja) * | 1993-11-10 | 2000-10-03 | ä¿¡è¶ååŠå·¥æ¥æ ªåŒäŒç€Ÿ | ç®è圢æçµæç© |
| FR2757529B1 (fr) * | 1996-12-24 | 1999-03-05 | Rhodia Chimie Sa | Compositions stables a base de polyorganosiloxanes a groupements fonctionnels reticulables et leur utilisation pour la realisation de revetements anti-adherents |
| US6277445B1 (en) * | 1998-10-12 | 2001-08-21 | Shin-Etsu Chemical Co., Ltd. | Organopolysiloxane compound and composition containing the same |
| US6255429B1 (en) * | 1999-09-02 | 2001-07-03 | Dow Corning Corporation | Amine-, polyol-, amide-functional siloxane copolymers and methods for their preparation |
| JP3404555B2 (ja) * | 1999-09-24 | 2003-05-12 | ãããœæ ªåŒäŒç€Ÿ | 芪氎æ§ç¹ç¶åã³äžç¹åžãããããçšããäžç¹åžå å·¥å |
| JP4597316B2 (ja) * | 2000-05-31 | 2010-12-15 | æ±ã¬ã»ããŠã³ãŒãã³ã°æ ªåŒäŒç€Ÿ | åæç¹ç¶åŠçå€çµæç© |
| US6649692B2 (en) | 2001-02-20 | 2003-11-18 | Crompton Corporation | Organopolysiloxane composition, emulsion-forming concentrates and aqueous emulsions formed therefrom and use of the emulsions in the treatment of textiles |
| EP1258503A1 (de) * | 2001-05-15 | 2002-11-20 | Clariant International Ltd. | Modifizierte Polyorganosiloxane, wÀssrige Emulsionen davon, ihre Herstellung und Verwendung |
| DE112004000559B4 (de) * | 2003-04-01 | 2014-05-28 | Matsumoto Yushi-Seiyaku Co., Ltd. | WasserdurchlÀssiges Mittel und Faser, auf die das wasserdurchlÀssige Mittel aufgetragen worden ist |
| DE102004013795A1 (de) * | 2004-03-20 | 2004-10-28 | Clariant Gmbh | Kosmetische oder pharmazeutische Mittel, enthaltend modifizierte Polyorganosiloxane |
| US7511165B2 (en) * | 2004-10-04 | 2009-03-31 | Clariant Finance (Bvi) Limited | Amino-functional silicone waxes |
| DE102005039511A1 (de) * | 2005-08-20 | 2007-02-22 | Clariant Produkte (Deutschland) Gmbh | Verwendung von quaternÀren Polysiloxanen in Reinigungs- und Pflegemitteln |
| CN100412262C (zh) * | 2006-09-07 | 2008-08-20 | æµæ±äŒ åè¡ä»œæéå ¬åž | ææºç¡ ç»ç©å¹³æ»åçå¶å€æ¹æ³ |
| WO2008127519A1 (en) | 2007-04-11 | 2008-10-23 | Dow Corning Corporation | Silcone polyether block copolymers having organofunctional endblocking groups |
| DE102007047863A1 (de) * | 2007-11-26 | 2009-05-28 | Wacker Chemie Ag | QuaternÀre Ammoniumgruppen aufweisende Organopolysiloxane, deren Herstellung und Verwendung |
| ES2391913T3 (es) * | 2008-06-13 | 2012-12-03 | Clariant Finance (Bvi) Limited | Composiciones cosméticas o farmacéuticas que comprenden polisiloxanos modificados con al menos un grupo carbamato |
| CA2794672A1 (en) * | 2010-04-01 | 2011-10-06 | The Procter & Gamble Company | Compositions comprising organosilicones |
| US8329255B2 (en) * | 2010-11-05 | 2012-12-11 | Momentive Performance Materials Inc. | Durable non-fluorine water repellent agent and process for preparing same |
| WO2013032493A1 (en) | 2011-08-26 | 2013-03-07 | Colgate-Palmolive Company | Fabric wrinkle reduction composition |
| CN105111444A (zh) * | 2015-08-25 | 2015-12-02 | å°é³å€©æºåå·¥æéå ¬åž | äžç§å 亮平æ»åçå¶é æ¹æ³ |
| CN113461969B (zh) * | 2021-07-16 | 2022-03-08 | 广å·åžä»²æ² å ¶æ°åæææéå ¬åž | äžç§ææºå®èœå¢æ¹æ§èç¡ æ°§ç·èå乳液åå¶å€æ¹æ³ |
| CN115353629B (zh) * | 2022-09-27 | 2024-01-23 | åå±±äžåç¡ äžè¡ä»œæéå ¬åž | ç¯æ°§ææºèç¡ æ°§ç·çå¶å€æ¹æ³ |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61159427A (ja) * | 1984-12-29 | 1986-07-19 | Toshiba Silicone Co Ltd | è¡šé¢åŠççšããªãªã«ã¬ãã·ãããµã³çµæç© |
| US4797446A (en) * | 1985-10-15 | 1989-01-10 | Dow Corning Corporation | Adhesion of silicone sealant |
-
1988
- 1988-02-27 JP JP63045352A patent/JPH01221580A/ja active Granted
-
1989
- 1989-02-25 KR KR1019890002267A patent/KR930005939B1/ko not_active IP Right Cessation
- 1989-02-27 US US07/315,879 patent/US5025076A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01221580A (ja) | 1989-09-05 |
| KR890013275A (ko) | 1989-09-22 |
| US5025076A (en) | 1991-06-18 |
| KR930005939B1 (ko) | 1993-06-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |