SK4492003A3 - Amphiphilic copolymers for use in particular as emulsifying agent - Google Patents
Amphiphilic copolymers for use in particular as emulsifying agent Download PDFInfo
- Publication number
- SK4492003A3 SK4492003A3 SK449-2003A SK4492003A SK4492003A3 SK 4492003 A3 SK4492003 A3 SK 4492003A3 SK 4492003 A SK4492003 A SK 4492003A SK 4492003 A3 SK4492003 A3 SK 4492003A3
- Authority
- SK
- Slovakia
- Prior art keywords
- amphiphilic
- copolymers
- copolymer
- water
- poly
- Prior art date
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 81
- 239000003995 emulsifying agent Substances 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 10
- 229920002223 polystyrene Polymers 0.000 claims abstract description 10
- 239000002250 absorbent Substances 0.000 claims abstract description 8
- 230000002745 absorbent Effects 0.000 claims abstract description 7
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 claims description 48
- 239000002202 Polyethylene glycol Substances 0.000 claims description 44
- 229920001223 polyethylene glycol Polymers 0.000 claims description 41
- 150000002433 hydrophilic molecules Chemical class 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 21
- 239000005977 Ethylene Substances 0.000 claims description 15
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 15
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
- 229920000469 amphiphilic block copolymer Polymers 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical group O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 claims description 11
- 239000004793 Polystyrene Substances 0.000 claims description 9
- 229920001451 polypropylene glycol Polymers 0.000 claims description 5
- 238000005886 esterification reaction Methods 0.000 claims description 4
- 229920001169 thermoplastic Polymers 0.000 claims description 4
- 239000004416 thermosoftening plastic Substances 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical class COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 2
- 239000003377 acid catalyst Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- -1 poly(styrene) Polymers 0.000 abstract description 9
- 239000000126 substance Substances 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 56
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 28
- 229920000642 polymer Polymers 0.000 description 25
- 229920002633 Kraton (polymer) Polymers 0.000 description 23
- 239000000047 product Substances 0.000 description 23
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 239000003921 oil Substances 0.000 description 18
- 238000010521 absorption reaction Methods 0.000 description 17
- 239000000839 emulsion Substances 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 150000008064 anhydrides Chemical group 0.000 description 10
- 230000002209 hydrophobic effect Effects 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 238000005259 measurement Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 229920000604 Polyethylene Glycol 200 Polymers 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 229920002594 Polyethylene Glycol 8000 Polymers 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 230000008859 change Effects 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 238000001556 precipitation Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 206010052428 Wound Diseases 0.000 description 4
- 208000027418 Wounds and injury Diseases 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000002537 cosmetic Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000010348 incorporation Methods 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 3
- 238000010533 azeotropic distillation Methods 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 210000004400 mucous membrane Anatomy 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
- 229920002582 Polyethylene Glycol 600 Polymers 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000007764 o/w emulsion Substances 0.000 description 2
- 229920001983 poloxamer Polymers 0.000 description 2
- 229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 239000007762 w/o emulsion Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 206010011985 Decubitus ulcer Diseases 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 241000765083 Ondina Species 0.000 description 1
- 229920002507 Poloxamer 124 Polymers 0.000 description 1
- 229920000463 Poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) Polymers 0.000 description 1
- 239000004353 Polyethylene glycol 8000 Substances 0.000 description 1
- 208000004210 Pressure Ulcer Diseases 0.000 description 1
- 108010021119 Trichosanthin Proteins 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000017 mucous membrane irritation Toxicity 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- RARSHUDCJQSEFJ-UHFFFAOYSA-N p-Hydroxypropiophenone Chemical compound CCC(=O)C1=CC=C(O)C=C1 RARSHUDCJQSEFJ-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229940093448 poloxamer 124 Drugs 0.000 description 1
- 229920001993 poloxamer 188 Polymers 0.000 description 1
- 229940044519 poloxamer 188 Drugs 0.000 description 1
- 229920001992 poloxamer 407 Polymers 0.000 description 1
- 229940044476 poloxamer 407 Drugs 0.000 description 1
- 229940113115 polyethylene glycol 200 Drugs 0.000 description 1
- 229940057847 polyethylene glycol 600 Drugs 0.000 description 1
- 229940085678 polyethylene glycol 8000 Drugs 0.000 description 1
- 235000019446 polyethylene glycol 8000 Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000002255 vaccination Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000002569 water oil cream Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C08G81/024—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G
- C08G81/025—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G containing polyether sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/14—Esterification
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Medicinal Preparation (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
- Polyethers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0013447A FR2815636B1 (fr) | 2000-10-20 | 2000-10-20 | Nouveaux copolymeres amphiphiles utilisables notamment comme agent emulsionnant |
PCT/FR2001/003226 WO2002032391A1 (fr) | 2000-10-20 | 2001-10-18 | Copolymeres amphiphiles utilisables notamment comme agent emulsionnant |
Publications (1)
Publication Number | Publication Date |
---|---|
SK4492003A3 true SK4492003A3 (en) | 2003-09-11 |
Family
ID=8855548
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK449-2003A SK4492003A3 (en) | 2000-10-20 | 2001-10-18 | Amphiphilic copolymers for use in particular as emulsifying agent |
Country Status (19)
Country | Link |
---|---|
US (1) | US7144947B2 (xx) |
EP (1) | EP1328249B1 (xx) |
JP (1) | JP2004511629A (xx) |
CN (1) | CN1224377C (xx) |
AT (1) | ATE348126T1 (xx) |
AU (1) | AU2002210667A1 (xx) |
BG (1) | BG107741A (xx) |
CA (1) | CA2426251A1 (xx) |
DE (1) | DE60125216T2 (xx) |
EE (1) | EE200300160A (xx) |
ES (1) | ES2275742T3 (xx) |
FR (1) | FR2815636B1 (xx) |
HK (1) | HK1057341A1 (xx) |
HU (1) | HUP0302427A3 (xx) |
MX (1) | MXPA03003450A (xx) |
NO (1) | NO20031700L (xx) |
PL (1) | PL362121A1 (xx) |
SK (1) | SK4492003A3 (xx) |
WO (1) | WO2002032391A1 (xx) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2815636B1 (fr) | 2000-10-20 | 2006-02-10 | Lhd Lab Hygiene Dietetique | Nouveaux copolymeres amphiphiles utilisables notamment comme agent emulsionnant |
FR2838745B1 (fr) | 2002-04-17 | 2004-07-09 | Urgo Laboratoires | Emulsions solides a base d'elastomere thermoplastique |
FR2838748B1 (fr) * | 2002-04-17 | 2004-07-09 | Urgo Laboratoires | Nouvelles compositions adhesives thermofusibles hydrophiles |
BRPI0400438A (pt) * | 2004-04-07 | 2005-11-22 | Botica Com Farmaceutica Ltda | Composição cosmética oleosa com capacidade suspensora |
GB0417938D0 (en) * | 2004-08-12 | 2004-09-15 | Univ Bristol | Elastomeric material exhibiting reduced adhesion and chewing gum composition containing it |
WO2007089784A2 (en) | 2006-02-01 | 2007-08-09 | Hollister Incorporated | Methods of applying a hydrophilic coating to a substrate, and substrates having a hydrophilic coating |
NZ579205A (en) * | 2007-02-26 | 2012-03-30 | Revolymer Ltd | Chewing gum containing an amphiphilic polymer which controls the release of a drug or other biologically active material |
WO2008104547A1 (en) * | 2007-02-26 | 2008-09-04 | Revolymer Limited | Medicated chewing gum |
EP2214503A1 (en) * | 2007-10-15 | 2010-08-11 | Revolymer Limited | Solvent-free synthesis of amphiphilic polymeric material |
CN101302296B (zh) * | 2008-06-03 | 2010-08-25 | 江南大学 | 一种双亲性共聚物自组装胶束乳化剂的制备方法 |
WO2010042191A1 (en) | 2008-10-07 | 2010-04-15 | Ross Technology Corporation | Highly durable superhydrophobic, oleophobic and anti-icing coatings and methods and compositions for their preparation |
GB0920879D0 (en) * | 2009-11-27 | 2010-01-13 | Revolymer Ltd | Cosmetic composition |
BR112013021231A2 (pt) | 2011-02-21 | 2019-09-24 | Ross Tech Corporation | revestimentos super-hidrofóbicos e oleofóbicos com sistemas ligantes de baixo voc |
WO2013090939A1 (en) | 2011-12-15 | 2013-06-20 | Ross Technology Corporation | Composition and coating for superhydrophobic performance |
CA2878189C (en) * | 2012-06-25 | 2021-07-13 | Ross Technology Corporation | Elastomeric coatings having hydrophobic and/or oleophobic properties |
GB201308916D0 (en) * | 2013-05-17 | 2013-07-03 | Revolymer Ltd | latex additives |
WO2014185927A1 (en) * | 2013-05-17 | 2014-11-20 | Colgate-Palmolive Company | Cleaner composition |
CN107096390B (zh) * | 2017-05-17 | 2019-12-06 | 四川理工学院 | 一种改性共聚物多孔膜的制备方法 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4369284A (en) * | 1977-03-17 | 1983-01-18 | Applied Elastomerics, Incorporated | Thermoplastic elastomer gelatinous compositions |
US5167649A (en) * | 1988-08-22 | 1992-12-01 | Zook Gerald P | Drug delivery system for the removal of dermal lesions |
ZA899629B (en) * | 1988-12-22 | 1990-09-26 | Ferro Corp | Toughened compositions of polyamide and functionalized rubber block or graft copolymers |
USH1022H (en) * | 1991-01-09 | 1992-02-04 | Shell Oil Company | Soft paintable polymer composition |
JPH05279623A (ja) * | 1992-03-31 | 1993-10-26 | Nippon Steel Chem Co Ltd | 塗料組成物 |
EP0723571B1 (en) | 1993-10-12 | 1998-12-02 | H.B. Fuller Licensing & Financing, Inc. | Polystyrene-ethylene/butylene-polystyrene hot melt adhesive |
KR970700743A (ko) * | 1993-12-29 | 1997-02-12 | 해리 제이. 그윈넬 | 수분산성 접착제 조성물 및 방법(water-dispersible adhesive composition and process) |
US5559165A (en) | 1995-08-08 | 1996-09-24 | National Starch And Chemical Investment Holding Corporation | Hot melt adhesives for bonding to sensitive areas of the human body |
EP0885942A1 (en) | 1997-06-17 | 1998-12-23 | H.B. Fuller Licensing & Financing, Inc. | Adhesive hotmelt formulation and articles constructed therefrom |
JP4323797B2 (ja) * | 2000-07-07 | 2009-09-02 | エイ.ブイ.トップチーブ インスティテュート オブ ペトロケミカル シンセシス | 最適化した接着特性を有する親水性感圧接着剤の調製 |
FR2814170B1 (fr) | 2000-09-18 | 2005-05-27 | Rhodia Chimie Sa | Nouveau latex a proprietes de surface modifiees par l' ajout d'un copolymere hydrosoluble a caractere amphiphile |
FR2815636B1 (fr) | 2000-10-20 | 2006-02-10 | Lhd Lab Hygiene Dietetique | Nouveaux copolymeres amphiphiles utilisables notamment comme agent emulsionnant |
US6918929B2 (en) * | 2003-01-24 | 2005-07-19 | Medtronic Vascular, Inc. | Drug-polymer coated stent with pegylated styrenic block copolymers |
-
2000
- 2000-10-20 FR FR0013447A patent/FR2815636B1/fr not_active Expired - Fee Related
-
2001
- 2001-10-18 ES ES01978563T patent/ES2275742T3/es not_active Expired - Lifetime
- 2001-10-18 PL PL01362121A patent/PL362121A1/xx unknown
- 2001-10-18 AU AU2002210667A patent/AU2002210667A1/en not_active Abandoned
- 2001-10-18 JP JP2002535630A patent/JP2004511629A/ja active Pending
- 2001-10-18 MX MXPA03003450A patent/MXPA03003450A/es active IP Right Grant
- 2001-10-18 DE DE60125216T patent/DE60125216T2/de not_active Expired - Lifetime
- 2001-10-18 WO PCT/FR2001/003226 patent/WO2002032391A1/fr not_active Application Discontinuation
- 2001-10-18 EP EP01978563A patent/EP1328249B1/fr not_active Expired - Lifetime
- 2001-10-18 SK SK449-2003A patent/SK4492003A3/sk unknown
- 2001-10-18 EE EEP200300160A patent/EE200300160A/xx unknown
- 2001-10-18 AT AT01978563T patent/ATE348126T1/de not_active IP Right Cessation
- 2001-10-18 CA CA002426251A patent/CA2426251A1/en not_active Abandoned
- 2001-10-18 HU HU0302427A patent/HUP0302427A3/hu unknown
- 2001-10-18 US US10/399,698 patent/US7144947B2/en not_active Expired - Fee Related
- 2001-10-18 CN CNB018176933A patent/CN1224377C/zh not_active Expired - Fee Related
-
2003
- 2003-04-11 NO NO20031700A patent/NO20031700L/no not_active Application Discontinuation
- 2003-04-18 BG BG107741A patent/BG107741A/xx unknown
-
2004
- 2004-01-14 HK HK04100254A patent/HK1057341A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP1328249A1 (fr) | 2003-07-23 |
NO20031700L (no) | 2003-06-03 |
US20040097624A1 (en) | 2004-05-20 |
AU2002210667A1 (en) | 2002-04-29 |
WO2002032391A1 (fr) | 2002-04-25 |
FR2815636B1 (fr) | 2006-02-10 |
CN1224377C (zh) | 2005-10-26 |
HUP0302427A3 (en) | 2005-10-28 |
DE60125216T2 (de) | 2007-10-25 |
MXPA03003450A (es) | 2003-07-14 |
NO20031700D0 (no) | 2003-04-11 |
ATE348126T1 (de) | 2007-01-15 |
FR2815636A1 (fr) | 2002-04-26 |
CA2426251A1 (en) | 2002-04-25 |
CN1469732A (zh) | 2004-01-21 |
PL362121A1 (en) | 2004-10-18 |
EE200300160A (et) | 2003-06-16 |
ES2275742T3 (es) | 2007-06-16 |
JP2004511629A (ja) | 2004-04-15 |
HK1057341A1 (en) | 2004-04-02 |
DE60125216D1 (de) | 2007-01-25 |
HUP0302427A2 (hu) | 2003-10-28 |
EP1328249B1 (fr) | 2006-12-13 |
BG107741A (en) | 2004-02-27 |
US7144947B2 (en) | 2006-12-05 |
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