DE60304992T2 - Supramolekularpolymere - Google Patents
Supramolekularpolymere Download PDFInfo
- Publication number
- DE60304992T2 DE60304992T2 DE60304992T DE60304992T DE60304992T2 DE 60304992 T2 DE60304992 T2 DE 60304992T2 DE 60304992 T DE60304992 T DE 60304992T DE 60304992 T DE60304992 T DE 60304992T DE 60304992 T2 DE60304992 T2 DE 60304992T2
- Authority
- DE
- Germany
- Prior art keywords
- polymer according
- functions
- additive
- polymer
- monomer
- 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
- 229920002677 supramolecular polymer Polymers 0.000 title claims abstract description 16
- 239000000178 monomer Substances 0.000 claims abstract description 29
- 229920000642 polymer Polymers 0.000 claims abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 17
- 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 compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000001301 oxygen Substances 0.000 claims abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 32
- 239000000654 additive Substances 0.000 claims description 21
- 239000004202 carbamide Substances 0.000 claims description 16
- 230000000996 additive effect Effects 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- 229920002647 polyamide Polymers 0.000 claims description 7
- 239000012943 hotmelt Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 5
- 239000004952 Polyamide Substances 0.000 claims description 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
- 239000000314 lubricant Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 3
- 230000002441 reversible effect Effects 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 238000004064 recycling Methods 0.000 claims description 2
- 239000006254 rheological additive Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 239000012815 thermoplastic material Substances 0.000 claims description 2
- 239000004416 thermosoftening plastic Substances 0.000 claims description 2
- 239000004593 Epoxy Substances 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims 1
- 230000006378 damage Effects 0.000 claims 1
- 230000006855 networking Effects 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- 125000000524 functional group Chemical group 0.000 abstract 5
- 239000005864 Sulphur Substances 0.000 abstract 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 19
- 239000000047 product Substances 0.000 description 18
- 229920000768 polyamine Polymers 0.000 description 8
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 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 group 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 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
- 230000005494 condensation Effects 0.000 description 5
- 239000010413 mother solution Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000004584 polyacrylic acid Substances 0.000 description 4
- 239000004810 polytetrafluoroethylene Substances 0.000 description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 4
- 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 4
- 239000000126 substance Substances 0.000 description 4
- 239000003784 tall oil Substances 0.000 description 4
- 0 CN(CCN1)C1=* Chemical compound CN(CCN1)C1=* 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- -1 ethylene amines Chemical class 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000013638 trimer Substances 0.000 description 3
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-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
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001735 carboxylic acids Chemical group 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- LPOUQGUYVMSQOH-UHFFFAOYSA-N n'-[2-(2-piperazin-1-ylethylamino)ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCN1CCNCC1 LPOUQGUYVMSQOH-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000003921 oil Substances 0.000 description 2
- 239000007793 ph indicator Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-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
- 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
- RVUHUHUXQMCLGN-UHFFFAOYSA-N 1-[2-(2-oxoimidazolidin-1-yl)ethyl]imidazolidin-2-one Chemical compound O=C1NCCN1CCN1C(=O)NCC1 RVUHUHUXQMCLGN-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
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- UPANVVPVAPXMCY-UHFFFAOYSA-N 4-piperazin-1-ylbutane-1,3-diamine Chemical compound NCCC(N)CN1CCNCC1 UPANVVPVAPXMCY-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 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
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 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
- 150000004985 diamines Chemical class 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920006334 epoxy coating Polymers 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 230000009477 glass transition Effects 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
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- WBIWIXJUBVWKLS-UHFFFAOYSA-N n'-(2-piperazin-1-ylethyl)ethane-1,2-diamine Chemical compound NCCNCCN1CCNCC1 WBIWIXJUBVWKLS-UHFFFAOYSA-N 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 238000005554 pickling 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
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000013557 residual solvent Substances 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
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)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0200596 | 2002-01-17 | ||
| FR0200596 | 2002-01-17 | ||
| PCT/FR2003/000114 WO2003059964A2 (fr) | 2002-01-17 | 2003-01-15 | Polymeres supramoleculaires |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60304992D1 DE60304992D1 (de) | 2006-06-08 |
| DE60304992T2 true DE60304992T2 (de) | 2007-01-18 |
Family
ID=8871343
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60304992T Expired - Lifetime DE60304992T2 (de) | 2002-01-17 | 2003-01-15 | Supramolekularpolymere |
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) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1465930B1 (fr) * | 2002-01-17 | 2006-05-03 | Arkema | Polymeres supramoleculaires |
| DE10335673B4 (de) * | 2003-08-04 | 2007-01-18 | Celanese Emulsions Gmbh | Wässrige Dispersionsklebstoffe, Verfahren zu deren Herstellung und deren Verwendung |
| JP4440888B2 (ja) | 2003-11-04 | 2010-03-24 | スプラポリックス・ビー．ブイ． | 重合体幹内に４重水素結合単位を含む超分子重合体の製造 |
| DE602005018932D1 (de) * | 2004-07-08 | 2010-03-04 | Arkema France | Polymermaterial mit ketten mit imidazolidonfunktionen |
| EP1773903B1 (en) | 2004-07-12 | 2017-08-09 | SupraPolix B.V. | Supramolecular ionomers |
| FR2882061B1 (fr) * | 2005-02-15 | 2008-04-18 | Arkema Sa | Materiaux elastiques |
| JP5130201B2 (ja) | 2005-05-04 | 2013-01-30 | スープラポリックス ビー．ブイ． | モジュール式生体吸収性又は生物医学用生物活性超分子材料 |
| FR2905697B1 (fr) * | 2006-09-08 | 2012-08-31 | Arkema France | Polymeres supramoleculaires semi-cristallins |
| FR2905698B1 (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 |
| ATE517970T1 (de) * | 2008-02-20 | 2011-08-15 | Ceca Sa | Bitumenhaltige zusammensetzungen |
| FR2930777B1 (fr) * | 2008-05-05 | 2011-07-01 | Arkema France | Procede de synthese de materiaux supramoleculaires |
| FR2932491B1 (fr) * | 2008-06-13 | 2010-08-27 | Bostik Sa | Nouvelle composition adhesive thermofusible a base de polyamide |
| 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 |
| FR2949232B1 (fr) | 2009-08-18 | 2011-10-28 | Ceca Sa | Composition bitumineuse contenant un polymer supramoleculaire |
| FR2950351B1 (fr) | 2009-09-23 | 2011-11-18 | Arkema France | Composition comprenant un melange d'elastomere et de polymere supramoleculaire |
| DK2504353T4 (da) | 2009-11-23 | 2023-11-20 | Cubist Pharmaceuticals Llc | Lipopeptidsammensætninger og tilsvarende fremgangsmåder |
| WO2011079008A1 (en) * | 2009-12-21 | 2011-06-30 | Schlumberger Canada Limited | Hydrogen bonding material for oilfield application |
| FR2959233B1 (fr) * | 2010-04-27 | 2013-09-06 | Arkema France | Molecules porteuses de groupes associatifs et leur utilisation comme plastifiants |
| FR2959232B1 (fr) * | 2010-04-27 | 2013-09-06 | Arkema France | Utilisation de molecules porteuses de groupes associatifs comme plastifiant |
| FR2966465B1 (fr) | 2010-10-21 | 2012-11-02 | Arkema France | Composition comprenant un melange de polycondensat thermoplastique et de polymere supramoleculaire, et procede de fabrication |
| US9006386B2 (en) | 2010-11-05 | 2015-04-14 | Suprapolix B.V. | Process for the preparation of a supramolecular polymer |
| JP5579028B2 (ja) * | 2010-11-19 | 2014-08-27 | 日東電工株式会社 | 水分散型粘着剤組成物、および粘着製品並びにその製造方法 |
| CN103842407B (zh) | 2011-08-02 | 2017-10-31 | 索尔维特殊聚合物意大利有限公司 | (全)氟聚合物组合物 |
| FR3002538B1 (fr) | 2013-02-25 | 2017-09-01 | Arkema France | Materiaux supramoleculaires a base d'oligo-amides |
| US9557479B2 (en) * | 2015-06-15 | 2017-01-31 | The Boeing Company | Multilayer system having reconfigurable dynamic structure reinforcement using nanoparticle embedded supramolecular adhesive and method |
| CN111491969B (zh) | 2017-12-21 | 2022-05-24 | 毕克化学有限公司 | 含脲基的抗流挂流变控制剂 |
| US20220073670A1 (en) | 2019-01-04 | 2022-03-10 | Byk-Chemie Gmbh | Urea group containing rheology control additive |
| EP3938418B1 (en) | 2019-03-14 | 2025-08-20 | BYK-Chemie GmbH | Rheology control additive containing cyclic amides |
| US20240002582A1 (en) | 2020-12-04 | 2024-01-04 | Byk-Chemie Gmbh | Rheology control agent |
| CN113096748B (zh) * | 2021-04-13 | 2022-07-12 | 中山大学 | 一种基于范德华势能的晶体结构的去重方法及系统 |
| CN119403890A (zh) | 2022-07-06 | 2025-02-07 | 毕克化学有限公司 | 包含环状酰胺的组合物 |
| JPWO2024135791A1 (enExample) * | 2022-12-21 | 2024-06-27 |
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| US2517750A (en) * | 1943-04-01 | 1950-08-08 | Union Carbide & Carbon Corp | Preparation of imidazolidones |
| US2613212A (en) * | 1950-10-26 | 1952-10-07 | Rohm & Haas | Imidazolidone derivatives |
| US4111877A (en) * | 1976-07-29 | 1978-09-05 | Air Products & Chemicals, Inc. | Allyl esters of n-alkyl-omega-(alkyleneureido) amic acids and their synthesis and use in aqueous emulsion polymer systems |
| DD212258A1 (de) * | 1982-12-09 | 1984-08-08 | Bitterfeld Chemie | Verfahren zur herstellung von selektiven adsobentien auf acrylatbasis |
| US4544609A (en) | 1984-09-12 | 1985-10-01 | Sun Chemical Corporation | Compounds and their use as insolubilizers for binders for paper coating compositions |
| IT1183524B (it) * | 1985-03-29 | 1987-10-22 | Enichem Sintesi | Composizioni di polimeri termoplastici autoestinguenti |
| DE3789337T2 (de) * | 1986-08-29 | 1994-08-11 | Nippon Zeon Co | Vulkanisierbare Elastomerzusammensetzung. |
| US5023739A (en) * | 1988-02-15 | 1991-06-11 | Matsushita Electric Industrial Co., Ltd. | Tape cassette with a trapping layer having a corrosiveness which is equal to or higher than that of the magnetic recording layer on the tape |
| JP2692150B2 (ja) * | 1988-07-08 | 1997-12-17 | 住友化学工業株式会社 | エポキシ基含有加硫性エラストマー組成物 |
| CA2006849A1 (en) * | 1988-12-29 | 1990-06-29 | Hiroyuki Sakamoto | Aqueous coating composition |
| US5334888A (en) | 1993-04-19 | 1994-08-02 | Intel Corporation | Fast exclusive-or and exclusive-nor gates |
| US5422042A (en) * | 1993-11-19 | 1995-06-06 | Huntsman Corporation | Imidazolidone polyetheramine strength enhancing additives of epoxy resin systems |
| AU3408297A (en) | 1996-06-24 | 1998-01-14 | Cytec Technology Corp. | Novel polymerizable acyl imidazolidinone monomers |
| NL1004192C2 (nl) | 1996-10-04 | 1998-04-07 | Dsm Nv | Supramoleculair polymeer. |
| TW486475B (en) * | 1996-12-26 | 2002-05-11 | Ube Industries | Acid addition salt of optically active piperidine compound and process for preparing the same |
| US6087448A (en) * | 1997-11-19 | 2000-07-11 | Amcol International Corporation | Solid superabsorbent material containing a poly(vinylguanidine) and an acidic water-absorbing resin |
| US5930089A (en) * | 1998-03-13 | 1999-07-27 | Hewlett-Packard Company | Head cleaner for linear tape drive |
| US6067212A (en) * | 1998-08-25 | 2000-05-23 | Hewlett-Packard Company | Tape drive head cleaner embedded in cartridge/drive leader block |
| US6215618B1 (en) * | 1998-11-06 | 2001-04-10 | Hewlett-Packard Co. | Linear tape drive head cleaning process |
| US6515827B1 (en) * | 1999-07-08 | 2003-02-04 | Storage Technology Corporation | Dual chambered environmentally controlled cartridge and method for protecting data storage media |
| US6638622B2 (en) * | 2001-01-11 | 2003-10-28 | Hitachi Global Storage Technologies | Perfluorinated polyethers with metal carboxylate end groups as anti-wetting and corrosion-protective agents |
| EP1465930B1 (fr) * | 2002-01-17 | 2006-05-03 | Arkema | Polymeres supramoleculaires |
-
2003
- 2003-01-15 EP EP03712245A patent/EP1465930B1/fr not_active Expired - Lifetime
- 2003-01-15 WO PCT/FR2003/000114 patent/WO2003059964A2/fr not_active Ceased
- 2003-01-15 AT AT03712245T patent/ATE325140T1/de active
- 2003-01-15 DE DE60304992T patent/DE60304992T2/de not_active Expired - Lifetime
- 2003-01-15 AU AU2003216726A patent/AU2003216726A1/en not_active Abandoned
- 2003-01-15 JP JP2003560064A patent/JP2005514498A/ja active Pending
- 2003-01-15 ES ES03712245T patent/ES2263962T3/es not_active Expired - Lifetime
- 2003-01-15 US US10/503,610 patent/US7250487B2/en not_active Expired - Lifetime
-
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
-
2009
- 2009-11-27 JP JP2009269623A patent/JP5554549B2/ja not_active Expired - Fee Related
-
2012
- 2012-12-19 JP JP2012276741A patent/JP2013100512A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US7250487B2 (en) | 2007-07-31 |
| AU2003216726A1 (en) | 2003-07-30 |
| WO2003059964A3 (fr) | 2004-03-11 |
| US7750113B2 (en) | 2010-07-06 |
| JP2010106277A (ja) | 2010-05-13 |
| JP5554549B2 (ja) | 2014-07-23 |
| JP2005514498A (ja) | 2005-05-19 |
| ATE325140T1 (de) | 2006-06-15 |
| ES2263962T3 (es) | 2006-12-16 |
| JP2013100512A (ja) | 2013-05-23 |
| US20070123694A1 (en) | 2007-05-31 |
| WO2003059964A2 (fr) | 2003-07-24 |
| US7348397B2 (en) | 2008-03-25 |
| US20050148760A1 (en) | 2005-07-07 |
| US20080167442A1 (en) | 2008-07-10 |
| DE60304992D1 (de) | 2006-06-08 |
| AU2003216726A8 (en) | 2003-07-30 |
| EP1465930B1 (fr) | 2006-05-03 |
| EP1465930A2 (fr) | 2004-10-13 |
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Owner name: ARKEMA FRANCE, PUTEAUX, FR |
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