SE524174C2 - Förfarande för framställning av en dendritisk polyeter - Google Patents
Förfarande för framställning av en dendritisk polyeterInfo
- Publication number
- SE524174C2 SE524174C2 SE0004155A SE0004155A SE524174C2 SE 524174 C2 SE524174 C2 SE 524174C2 SE 0004155 A SE0004155 A SE 0004155A SE 0004155 A SE0004155 A SE 0004155A SE 524174 C2 SE524174 C2 SE 524174C2
- Authority
- SE
- Sweden
- Prior art keywords
- propanediol
- alkyl
- process according
- oxetane
- alkoxy
- Prior art date
Links
- 229920000570 polyether Polymers 0.000 title claims abstract description 37
- 239000004721 Polyphenylene oxide Substances 0.000 title claims abstract description 30
- 238000004519 manufacturing process Methods 0.000 title abstract description 4
- 238000000034 method Methods 0.000 claims abstract description 40
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 35
- 238000006243 chemical reaction Methods 0.000 claims abstract description 27
- 150000001875 compounds Chemical class 0.000 claims abstract description 27
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000003999 initiator Substances 0.000 claims abstract description 17
- 239000000203 mixture Substances 0.000 claims abstract description 15
- 238000007151 ring opening polymerisation reaction Methods 0.000 claims abstract description 10
- 125000002091 cationic group Chemical group 0.000 claims abstract description 9
- 238000007142 ring opening reaction Methods 0.000 claims abstract description 9
- DWYJHMSKXMHOAP-UHFFFAOYSA-N oxetan-2-ol Chemical compound OC1CCO1 DWYJHMSKXMHOAP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000003566 oxetanyl group Chemical group 0.000 claims abstract description 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 32
- 229940035437 1,3-propanediol Drugs 0.000 claims description 32
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 32
- 125000003545 alkoxy group Chemical group 0.000 claims description 27
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 21
- 239000000178 monomer Substances 0.000 claims description 21
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 14
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- -1 ethoxy, propoxy, butoxy, phenylethoxy Chemical group 0.000 claims description 11
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 11
- UNMJLQGKEDTEKJ-UHFFFAOYSA-N (3-ethyloxetan-3-yl)methanol Chemical compound CCC1(CO)COC1 UNMJLQGKEDTEKJ-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 7
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 6
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 229920000728 polyester Polymers 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 4
- 239000000539 dimer Substances 0.000 claims description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 4
- 239000013638 trimer Substances 0.000 claims description 4
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims description 4
- WMYINDVYGQKYMI-UHFFFAOYSA-N 2-[2,2-bis(hydroxymethyl)butoxymethyl]-2-ethylpropane-1,3-diol Chemical compound CCC(CO)(CO)COCC(CC)(CO)CO WMYINDVYGQKYMI-UHFFFAOYSA-N 0.000 claims description 3
- BQSZNEVPSCKFPQ-UHFFFAOYSA-N propane-1,2,2,3-tetrol Chemical compound OCC(O)(O)CO BQSZNEVPSCKFPQ-UHFFFAOYSA-N 0.000 claims description 3
- NLQMSBJFLQPLIJ-UHFFFAOYSA-N (3-methyloxetan-3-yl)methanol Chemical group OCC1(C)COC1 NLQMSBJFLQPLIJ-UHFFFAOYSA-N 0.000 claims description 2
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 claims description 2
- VNAWKNVDKFZFSU-UHFFFAOYSA-N 2-ethyl-2-methylpropane-1,3-diol Chemical compound CCC(C)(CO)CO VNAWKNVDKFZFSU-UHFFFAOYSA-N 0.000 claims description 2
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002841 Lewis acid Substances 0.000 claims description 2
- XDODWINGEHBYRT-UHFFFAOYSA-N [2-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCCC1CO XDODWINGEHBYRT-UHFFFAOYSA-N 0.000 claims description 2
- QSGREIXRTDCBHO-UHFFFAOYSA-N [3-(hydroxymethyl)oxetan-3-yl]methanol Chemical compound OCC1(CO)COC1 QSGREIXRTDCBHO-UHFFFAOYSA-N 0.000 claims description 2
- ZTISUHQLYYPYFA-UHFFFAOYSA-N [5-(hydroxymethyl)-1,3-dioxan-5-yl]methanol Chemical compound OCC1(CO)COCOC1 ZTISUHQLYYPYFA-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 claims description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims description 2
- 150000007517 lewis acids Chemical group 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 229920001451 polypropylene glycol Polymers 0.000 claims description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims 1
- 229910021630 Antimony pentafluoride Inorganic materials 0.000 claims 1
- 229910017049 AsF5 Inorganic materials 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- 229910021174 PF5 Inorganic materials 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 229910004014 SiF4 Inorganic materials 0.000 claims 1
- 229910003074 TiCl4 Inorganic materials 0.000 claims 1
- VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 claims 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 claims 1
- YBGKQGSCGDNZIB-UHFFFAOYSA-N arsenic pentafluoride Chemical compound F[As](F)(F)(F)F YBGKQGSCGDNZIB-UHFFFAOYSA-N 0.000 claims 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims 1
- 150000002009 diols Chemical class 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 229940117969 neopentyl glycol Drugs 0.000 claims 1
- OBCUTHMOOONNBS-UHFFFAOYSA-N phosphorus pentafluoride Chemical compound FP(F)(F)(F)F OBCUTHMOOONNBS-UHFFFAOYSA-N 0.000 claims 1
- ABTOQLMXBSRXSM-UHFFFAOYSA-N silicon tetrafluoride Chemical compound F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 claims 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims 1
- 230000015556 catabolic process Effects 0.000 abstract description 4
- 238000006731 degradation reaction Methods 0.000 abstract description 3
- 239000000047 product Substances 0.000 description 20
- 238000010586 diagram Methods 0.000 description 18
- 238000010438 heat treatment Methods 0.000 description 18
- 239000000126 substance Substances 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 239000000412 dendrimer Substances 0.000 description 7
- 229920000736 dendritic polymer Polymers 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000000113 differential scanning calorimetry Methods 0.000 description 6
- 101001047746 Homo sapiens Lamina-associated polypeptide 2, isoform alpha Proteins 0.000 description 5
- 101001047731 Homo sapiens Lamina-associated polypeptide 2, isoforms beta/gamma Proteins 0.000 description 5
- 102100023981 Lamina-associated polypeptide 2, isoform alpha Human genes 0.000 description 5
- 238000013019 agitation Methods 0.000 description 5
- 239000012467 final product Substances 0.000 description 5
- 150000003384 small molecules Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 150000004292 cyclic ethers Chemical class 0.000 description 4
- 239000004970 Chain extender Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 239000003377 acid catalyst Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 229910018287 SbF 5 Inorganic materials 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000005055 alkyl alkoxy group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- SWYHWLFHDVMLHO-UHFFFAOYSA-N oxetan-3-ylmethanol Chemical compound OCC1COC1 SWYHWLFHDVMLHO-UHFFFAOYSA-N 0.000 description 1
- 150000002921 oxetanes Chemical class 0.000 description 1
- 125000000109 phenylethoxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])O* 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 238000004260 weight control 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
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/003—Dendrimers
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/16—Cyclic ethers having four or more ring atoms
- C08G65/18—Oxetanes
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0004155A SE524174C2 (sv) | 2000-11-14 | 2000-11-14 | Förfarande för framställning av en dendritisk polyeter |
| AU2002214502A AU2002214502A1 (en) | 2000-11-14 | 2001-11-12 | Process for manufacture of a dendritic polyether |
| US10/416,712 US7176264B2 (en) | 2000-11-14 | 2001-11-12 | Process for manufacture of a dendritic polyether |
| EP01983047.0A EP1355975B1 (fr) | 2000-11-14 | 2001-11-12 | Procede de fabrication d'un polyether dendritique |
| PCT/SE2001/002519 WO2002040572A1 (fr) | 2000-11-14 | 2001-11-12 | Procede de fabrication d'un polyether dendritique |
| JP2002543576A JP2004514037A (ja) | 2000-11-14 | 2001-11-12 | 樹枝状ポリエーテルの製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0004155A SE524174C2 (sv) | 2000-11-14 | 2000-11-14 | Förfarande för framställning av en dendritisk polyeter |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE0004155D0 SE0004155D0 (sv) | 2000-11-14 |
| SE0004155L SE0004155L (sv) | 2002-05-15 |
| SE524174C2 true SE524174C2 (sv) | 2004-07-06 |
Family
ID=20281805
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE0004155A SE524174C2 (sv) | 2000-11-14 | 2000-11-14 | Förfarande för framställning av en dendritisk polyeter |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7176264B2 (fr) |
| EP (1) | EP1355975B1 (fr) |
| JP (1) | JP2004514037A (fr) |
| AU (1) | AU2002214502A1 (fr) |
| SE (1) | SE524174C2 (fr) |
| WO (1) | WO2002040572A1 (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1440995B1 (fr) * | 2003-01-23 | 2019-08-07 | Rapp Polymere GmbH | Polymères portant les groupes hydroxyles |
| JP4639332B2 (ja) * | 2005-02-09 | 2011-02-23 | 学校法人神奈川大学 | デンドリック高分子、放射線硬化性デンドリック高分子、硬化物、及び、それらの製造方法 |
| CA2632576A1 (fr) * | 2005-12-22 | 2007-07-05 | Michael S. Ferritto | Polyglycols ramifies et polyorganosiloxanes ayant une fonction polyether ramifies et revetements contenant ceux-ci |
| DE102006031152A1 (de) * | 2006-07-04 | 2008-01-10 | Byk-Chemie Gmbh | Polyhydroxyfunktionelle Polysiloxane als anti-adhäsive und schmutzabweisende Zusätze in Beschichtungen, polymeren Formmassen und Thermoplasten, Verfahren zu ihrer Herstellung und ihre Verwendung |
| JP5383196B2 (ja) * | 2006-09-19 | 2014-01-08 | 新日鉄住金化学株式会社 | 熱重合性樹脂組成物 |
| DE102007026722A1 (de) * | 2007-06-06 | 2008-12-11 | Basf Coatings Japan Ltd., Yokohama | Klarlackzusammensetzungen enthaltend hyperverzweigte, dendritische hydroxyfunktionelle Polyester |
| DE102007026724A1 (de) * | 2007-06-06 | 2008-12-11 | Basf Coatings Japan Ltd., Yokohama | Bindemittel mit hoher OH-Zahl und sie enthaltende Klarlackzusammensetzungen mit guten optischen Eigenschaften und guter Kratz- und Chemikalienbeständigkeit |
| US20090314183A1 (en) * | 2008-06-24 | 2009-12-24 | S.D. Warren Company | Multi-component Starch Binder Compositions |
| DE102008032066A1 (de) | 2008-07-08 | 2010-01-14 | Byk-Chemie Gmbh | Polyhydroxyfunktionelle Polysiloxane als anti-adhäsive und schmutzabweisende Zusätze in Beschichtungen, polymeren Formmassen und Thermoplasten, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE102008032064A1 (de) | 2008-07-08 | 2010-01-14 | Byk-Chemie Gmbh | Polyhydroxyfunktionelle Polysiloxane zur Erhöhung der Oberflächenenergie von Thermoplasten, Verfahren zu ihrer Herstellug und ihre Verwendung |
| DE102009021913A1 (de) | 2009-05-19 | 2010-12-02 | Byk-Chemie Gmbh | Terminal ungesättigte, oxetan-basierte Makromonomere und Verfahren zu deren Herstellung |
| DE102009021912A1 (de) * | 2009-05-19 | 2010-12-02 | Byk-Chemie Gmbh | Aus oxetan-basierten Makromonomeren erhältliche Polymere, Verfahren zu deren Herstellung und deren Verwendung als Additive in Beschichtungsmitteln und Kunststoffen |
| DE102011076019A1 (de) | 2011-05-18 | 2012-11-22 | Evonik Goldschmidt Gmbh | Alkoxylierungsprodukte und Verfahren zu ihrer Herstellung mittels DMC-Katalysatoren |
| DE102011109614A1 (de) | 2011-08-03 | 2013-02-07 | Evonik Goldschmidt Gmbh | Verfahren zur Herstellung von verzweigten Polyethercarbonaten und ihre Verwendung |
| DE102011109541A1 (de) | 2011-08-03 | 2013-02-07 | Evonik Goldschmidt Gmbh | Verwendung von Polysiloxanen enthaltend verzweigte Polyetherreste zur Herstellung von Polyurethanschäumen |
| DE102011109545A1 (de) | 2011-08-03 | 2013-02-07 | Evonik Goldschmidt Gmbh | Verfahren zur Herstellung von Polyethersiloxanen enthaltend Polyethercarbonatgrundstrukturen |
| WO2018091448A1 (fr) | 2016-11-15 | 2018-05-24 | Byk-Chemie Gmbh | Polyéther à base d'oxétanes pour utilisation en tant qu'agents mouillants et dispersants, et leur utilisation |
| CN109937222B (zh) | 2016-11-15 | 2021-08-17 | 毕克化学有限公司 | 用作润湿剂和分散剂的基于氧杂环丁烷的聚醚及其生产 |
| CN110527109B (zh) * | 2019-09-03 | 2021-06-11 | 北京大学口腔医学院 | 一种多羟基超支化聚合物及制备方法以及其在牙科复合树脂中的应用 |
| CN110760071A (zh) * | 2019-10-12 | 2020-02-07 | 青岛大学 | 一种新型树枝状高粘稠油降粘剂的制备方法 |
| TWI781508B (zh) * | 2020-10-30 | 2022-10-21 | 財團法人工業技術研究院 | 樹脂與墨水 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2947722A (en) * | 1954-08-17 | 1960-08-02 | Hercules Powder Co Ltd | Stabilized polymeric oxetane molding compositions |
| FR2218351B1 (fr) * | 1973-02-16 | 1976-05-14 | Protex Manuf Prod Chimiq | |
| US4393199A (en) * | 1981-05-12 | 1983-07-12 | S R I International | Cationic polymerization |
| US4988797B1 (en) * | 1989-03-14 | 1993-12-28 | Cationic polymerization of cyclic ethers | |
| US5099042A (en) * | 1989-03-14 | 1992-03-24 | Thiokol Corporation | Synthesis of tetrafunctional polyethers and compositions formed therefrom |
| US4952644A (en) * | 1989-06-07 | 1990-08-28 | Thiokol Corporation | Synthesis of ABA triblock polymers and An B star polymers from cyclic ethers |
| US5516854A (en) * | 1990-07-27 | 1996-05-14 | Thiokol Corporation | Method of producing thermoplastic elastomers having alternate crystalline structure such as polyoxetane ABA or star block copolymers by a block linking process |
| SE514207C2 (sv) * | 1999-03-23 | 2001-01-22 | Perstorp Ab | Hyperförgrenad dendritisk polyeter och förfarande för framställning därav |
| SE520971C2 (sv) | 1999-08-20 | 2003-09-16 | Perstorp Ab | Förfarande för tillverkning av en eteralkohol |
-
2000
- 2000-11-14 SE SE0004155A patent/SE524174C2/sv unknown
-
2001
- 2001-11-12 AU AU2002214502A patent/AU2002214502A1/en not_active Abandoned
- 2001-11-12 WO PCT/SE2001/002519 patent/WO2002040572A1/fr not_active Ceased
- 2001-11-12 EP EP01983047.0A patent/EP1355975B1/fr not_active Expired - Lifetime
- 2001-11-12 JP JP2002543576A patent/JP2004514037A/ja active Pending
- 2001-11-12 US US10/416,712 patent/US7176264B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU2002214502A1 (en) | 2002-05-27 |
| JP2004514037A (ja) | 2004-05-13 |
| US20040059086A1 (en) | 2004-03-25 |
| SE0004155L (sv) | 2002-05-15 |
| EP1355975A1 (fr) | 2003-10-29 |
| US7176264B2 (en) | 2007-02-13 |
| WO2002040572A1 (fr) | 2002-05-23 |
| SE0004155D0 (sv) | 2000-11-14 |
| EP1355975B1 (fr) | 2016-08-31 |
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