JP2005514498A - 超分子ポリマー - Google Patents
超分子ポリマー Download PDFInfo
- Publication number
- JP2005514498A JP2005514498A JP2003560064A JP2003560064A JP2005514498A JP 2005514498 A JP2005514498 A JP 2005514498A JP 2003560064 A JP2003560064 A JP 2003560064A JP 2003560064 A JP2003560064 A JP 2003560064A JP 2005514498 A JP2005514498 A JP 2005514498A
- Authority
- JP
- Japan
- Prior art keywords
- supramolecular polymer
- polymer according
- groups
- supramolecular
- additive
- 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.)
- Pending
Links
- 229920002677 supramolecular polymer Polymers 0.000 title claims abstract description 38
- 239000000178 monomer Substances 0.000 claims abstract description 26
- 239000000203 mixture Substances 0.000 claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 13
- 239000001257 hydrogen Substances 0.000 claims abstract description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000001301 oxygen Substances 0.000 claims abstract description 9
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 3
- 239000011593 sulfur Chemical group 0.000 claims abstract description 3
- 239000000654 additive Substances 0.000 claims description 8
- 230000000996 additive effect Effects 0.000 claims description 7
- 239000003973 paint Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 229920002647 polyamide Polymers 0.000 claims description 5
- 239000004831 Hot glue Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 238000004132 cross linking Methods 0.000 claims description 3
- 230000002441 reversible effect Effects 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 239000006254 rheological additive Substances 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- 239000004609 Impact Modifier Substances 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 239000000314 lubricant Substances 0.000 claims 1
- 239000012815 thermoplastic material Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 7
- 239000003963 antioxidant agent Substances 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 37
- 239000004202 carbamide Substances 0.000 description 18
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 14
- 239000012452 mother liquor Substances 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 229920000768 polyamine Polymers 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 229920002125 Sokalan® Polymers 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 4
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000004584 polyacrylic acid Substances 0.000 description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 4
- 239000004810 polytetrafluoroethylene Substances 0.000 description 4
- 239000003784 tall oil Substances 0.000 description 4
- 0 CC(*CCNC)=* Chemical compound CC(*CCNC)=* 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- -1 polytetrafluoroethylene Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CZRCFAOMWRAFIC-UHFFFAOYSA-N 5-(tetradecyloxy)-2-furoic acid Chemical compound CCCCCCCCCCCCCCOC1=CC=C(C(O)=O)O1 CZRCFAOMWRAFIC-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000002843 carboxylic acid group Chemical group 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 2
- BNCPSJBACSAPHV-UHFFFAOYSA-N (2-oxo-1h-pyrimidin-6-yl)urea Chemical group NC(=O)NC=1C=CNC(=O)N=1 BNCPSJBACSAPHV-UHFFFAOYSA-N 0.000 description 1
- CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 1
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- BUVFKQKYSDYXNV-UHFFFAOYSA-N 1-(2-piperazin-1-ylethyl)imidazolidin-2-one Chemical compound O=C1NCCN1CCN1CCNCC1 BUVFKQKYSDYXNV-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- PAOXFRSJRCGJLV-UHFFFAOYSA-N 2-[4-(2-aminoethyl)piperazin-1-yl]ethanamine Chemical compound NCCN1CCN(CCN)CC1 PAOXFRSJRCGJLV-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 229920000891 common polymer Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical group O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- LPOUQGUYVMSQOH-UHFFFAOYSA-N n'-[2-(2-piperazin-1-ylethylamino)ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCN1CCNCC1 LPOUQGUYVMSQOH-UHFFFAOYSA-N 0.000 description 1
- CXNQJNPKMZRHBC-UHFFFAOYSA-N n'-[2-[4-(2-aminoethyl)piperazin-1-yl]ethyl]ethane-1,2-diamine Chemical compound NCCNCCN1CCN(CCN)CC1 CXNQJNPKMZRHBC-UHFFFAOYSA-N 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical group O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000005406 washing 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
-
- 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
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- 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
- C08F8/34—Introducing sulfur atoms or sulfur-containing groups
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/028—Polyamidoamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/02—Polyamines
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)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polyamides (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Lubricants (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0200596 | 2002-01-17 | ||
| PCT/FR2003/000114 WO2003059964A2 (fr) | 2002-01-17 | 2003-01-15 | Polymeres supramoleculaires |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009269623A Division JP5554549B2 (ja) | 2002-01-17 | 2009-11-27 | 超分子ポリマー |
| JP2012276741A Division JP2013100512A (ja) | 2002-01-17 | 2012-12-19 | 超分子ポリマー |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005514498A true JP2005514498A (ja) | 2005-05-19 |
| JP2005514498A5 JP2005514498A5 (enExample) | 2013-02-14 |
Family
ID=8871343
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003560064A Pending JP2005514498A (ja) | 2002-01-17 | 2003-01-15 | 超分子ポリマー |
| JP2009269623A Expired - Fee Related JP5554549B2 (ja) | 2002-01-17 | 2009-11-27 | 超分子ポリマー |
| JP2012276741A Withdrawn JP2013100512A (ja) | 2002-01-17 | 2012-12-19 | 超分子ポリマー |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009269623A Expired - Fee Related JP5554549B2 (ja) | 2002-01-17 | 2009-11-27 | 超分子ポリマー |
| JP2012276741A Withdrawn JP2013100512A (ja) | 2002-01-17 | 2012-12-19 | 超分子ポリマー |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US7250487B2 (enExample) |
| EP (1) | EP1465930B1 (enExample) |
| JP (3) | JP2005514498A (enExample) |
| AT (1) | ATE325140T1 (enExample) |
| AU (1) | AU2003216726A1 (enExample) |
| DE (1) | DE60304992T2 (enExample) |
| ES (1) | ES2263962T3 (enExample) |
| WO (1) | WO2003059964A2 (enExample) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010106277A (ja) * | 2002-01-17 | 2010-05-13 | Arkema France | 超分子ポリマー |
| JP2011522909A (ja) * | 2008-05-05 | 2011-08-04 | アルケマ フランス | 超分子材料の合成方法 |
| JP2011522946A (ja) * | 2008-06-13 | 2011-08-04 | ボスティク エス.アー. | 新規なポリアミドベースのホットメルト接着組成物 |
| KR101088660B1 (ko) * | 2006-09-08 | 2011-12-01 | 상뜨로 나쇼날 드 라 러쉐르쉐 샹띠피크 | 반결정성 초분자 중합체 |
| JP2013525562A (ja) * | 2010-04-27 | 2013-06-20 | アルケマ フランス | 結合基を担持している分子及び可塑剤としてのそれらの使用 |
| JP2013525563A (ja) * | 2010-04-27 | 2013-06-20 | アルケマ フランス | 会合性基を有している分子の可塑剤としての使用 |
| JP2013540193A (ja) * | 2010-10-21 | 2013-10-31 | アルケマ フランス | 熱可塑性縮合ポリマーおよび超分子ポリマーの混合物を含む組成物ならびに製造方法 |
| JP2017001386A (ja) * | 2015-06-15 | 2017-01-05 | ザ・ボーイング・カンパニーThe Boeing Company | ナノ粒子が埋め込まれた超分子接着剤を用いた再構成可能な動的構造補強システム |
| WO2024135791A1 (ja) * | 2022-12-21 | 2024-06-27 | 国立大学法人 東京大学 | 機械的に堅牢なサステイナブルプラスチック及びそのグリーンで非共有結合的な製造方法 |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10335673B4 (de) | 2003-08-04 | 2007-01-18 | Celanese Emulsions Gmbh | Wässrige Dispersionsklebstoffe, Verfahren zu deren Herstellung und deren Verwendung |
| US7838621B2 (en) | 2003-11-04 | 2010-11-23 | Suprapolix B.V. | Preparation of supramolecular polymer containing quadruple hydrogen bonding units in the polymer backbone |
| PL1778741T3 (pl) * | 2004-07-08 | 2010-06-30 | Arkema France | Materiał polimerowy zawierający łańcuchy niosące grupy funkcyjne imidazolidonu |
| US8268952B2 (en) | 2004-07-12 | 2012-09-18 | Suprapolix B.V. | Supramolecular ionomers |
| FR2882061B1 (fr) * | 2005-02-15 | 2008-04-18 | Arkema Sa | Materiaux elastiques |
| ATE532540T1 (de) | 2005-05-04 | 2011-11-15 | Suprapolix Bv | Modulare bioresorbierbare oder biomedizinische biologisch aktive supramolekulare stoffe |
| FR2905697B1 (fr) * | 2006-09-08 | 2012-08-31 | Arkema France | Polymeres supramoleculaires semi-cristallins |
| EP2087027B1 (en) | 2006-11-20 | 2011-10-05 | SupraPolix B.V. | Supramolecular polymers from low-melting, easily processable building blocks |
| US8628789B2 (en) | 2007-03-23 | 2014-01-14 | Suprapolix, B.V. | Strong reversible hydrogels |
| FR2924715B1 (fr) * | 2007-12-06 | 2012-10-12 | Arkema France | Materiau forme de molecules arborescentes comportant des groupes associatifs |
| FR2925505B1 (fr) * | 2007-12-24 | 2010-04-02 | Arkema France | Procede de preparation d'un materiau forme de molecules arborescentes comportant des groupes associatifs |
| PL2093274T3 (pl) | 2008-02-20 | 2011-12-30 | Ceca Sa | Kompozycje bitumiczne |
| FR2932489B1 (fr) * | 2008-06-17 | 2010-06-11 | Arkema France | Composition renfermant un polymere (meth)acrylique et un copolymere porteur de groupes associatifs |
| WO2010002262A1 (en) | 2008-07-04 | 2010-01-07 | Suprapolix B.V. | High flow supramolecular compounds |
| FR2944025B1 (fr) * | 2009-04-02 | 2011-04-01 | Arkema France | Utilisation en tant qu'absorbeur de chocs, d'un materiau forme de molecules arborescentes comportant des groupes associatifs |
| FR2948944B1 (fr) * | 2009-08-04 | 2012-10-05 | Ceca Sa | Supramolecular polymer-containing bituminous composition |
| FR2948942B1 (fr) * | 2009-08-06 | 2012-03-23 | Rhodia Operations | Polymeres supramoleculaires et materiaux a base desdits polymeres |
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| FR2950351B1 (fr) | 2009-09-23 | 2011-11-18 | Arkema France | Composition comprenant un melange d'elastomere et de polymere supramoleculaire |
| TWI548414B (zh) | 2009-11-23 | 2016-09-11 | 庫比斯特製藥有限責任公司 | 達托黴素(daptomycin)組合物及相關方法 |
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2003
- 2003-01-15 JP JP2003560064A patent/JP2005514498A/ja active Pending
- 2003-01-15 EP EP03712245A patent/EP1465930B1/fr not_active Expired - Lifetime
- 2003-01-15 AU AU2003216726A patent/AU2003216726A1/en not_active Abandoned
- 2003-01-15 WO PCT/FR2003/000114 patent/WO2003059964A2/fr not_active Ceased
- 2003-01-15 DE DE60304992T patent/DE60304992T2/de not_active Expired - Lifetime
- 2003-01-15 US US10/503,610 patent/US7250487B2/en not_active Expired - Lifetime
- 2003-01-15 ES ES03712245T patent/ES2263962T3/es not_active Expired - Lifetime
- 2003-01-15 AT AT03712245T patent/ATE325140T1/de active
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2006
- 2006-11-14 US US11/598,931 patent/US7348397B2/en not_active Expired - Lifetime
-
2008
- 2008-03-19 US US12/051,278 patent/US7750113B2/en not_active Expired - Fee Related
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2009
- 2009-11-27 JP JP2009269623A patent/JP5554549B2/ja not_active Expired - Fee Related
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2012
- 2012-12-19 JP JP2012276741A patent/JP2013100512A/ja not_active Withdrawn
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010106277A (ja) * | 2002-01-17 | 2010-05-13 | Arkema France | 超分子ポリマー |
| KR101088660B1 (ko) * | 2006-09-08 | 2011-12-01 | 상뜨로 나쇼날 드 라 러쉐르쉐 샹띠피크 | 반결정성 초분자 중합체 |
| JP2011522909A (ja) * | 2008-05-05 | 2011-08-04 | アルケマ フランス | 超分子材料の合成方法 |
| JP2011522946A (ja) * | 2008-06-13 | 2011-08-04 | ボスティク エス.アー. | 新規なポリアミドベースのホットメルト接着組成物 |
| JP2013525562A (ja) * | 2010-04-27 | 2013-06-20 | アルケマ フランス | 結合基を担持している分子及び可塑剤としてのそれらの使用 |
| JP2013525563A (ja) * | 2010-04-27 | 2013-06-20 | アルケマ フランス | 会合性基を有している分子の可塑剤としての使用 |
| JP2013540193A (ja) * | 2010-10-21 | 2013-10-31 | アルケマ フランス | 熱可塑性縮合ポリマーおよび超分子ポリマーの混合物を含む組成物ならびに製造方法 |
| JP2017001386A (ja) * | 2015-06-15 | 2017-01-05 | ザ・ボーイング・カンパニーThe Boeing Company | ナノ粒子が埋め込まれた超分子接着剤を用いた再構成可能な動的構造補強システム |
| WO2024135791A1 (ja) * | 2022-12-21 | 2024-06-27 | 国立大学法人 東京大学 | 機械的に堅牢なサステイナブルプラスチック及びそのグリーンで非共有結合的な製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1465930B1 (fr) | 2006-05-03 |
| US7348397B2 (en) | 2008-03-25 |
| DE60304992D1 (de) | 2006-06-08 |
| AU2003216726A1 (en) | 2003-07-30 |
| ATE325140T1 (de) | 2006-06-15 |
| US20050148760A1 (en) | 2005-07-07 |
| AU2003216726A8 (en) | 2003-07-30 |
| US20080167442A1 (en) | 2008-07-10 |
| JP5554549B2 (ja) | 2014-07-23 |
| US7750113B2 (en) | 2010-07-06 |
| JP2013100512A (ja) | 2013-05-23 |
| WO2003059964A2 (fr) | 2003-07-24 |
| JP2010106277A (ja) | 2010-05-13 |
| US20070123694A1 (en) | 2007-05-31 |
| ES2263962T3 (es) | 2006-12-16 |
| EP1465930A2 (fr) | 2004-10-13 |
| DE60304992T2 (de) | 2007-01-18 |
| US7250487B2 (en) | 2007-07-31 |
| WO2003059964A3 (fr) | 2004-03-11 |
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