SE524461C2 - Kedjeförlängd dendritisk polyeter, komposition samt användning därav - Google Patents

Kedjeförlängd dendritisk polyeter, komposition samt användning därav

Info

Publication number: SE524461C2
Authority: SE; Sweden
Prior art keywords: acid; chain; dendritic polyether; propanediol; oxetane
Prior art date: 2002-01-25

Application number

SE0200207A

Other languages

English (en)

Swedish (sv)

Other versions

SE0200207L (sv

SE0200207D0 (sv

Inventor

Bo Pettersson

David James

Haakan Bjoernberg

Birger Midelf

Original Assignee

Perstorp Specialty Chem Ab

Priority date (The priority date 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 date listed.)

2002-01-25

Filing date

2002-01-25

Publication date

2004-08-10

2002-01-25 Application filed by Perstorp Specialty Chem Ab filed Critical Perstorp Specialty Chem Ab

2002-01-25 Priority to SE0200207A priority Critical patent/SE524461C2/sv

2002-01-25 Publication of SE0200207D0 publication Critical patent/SE0200207D0/xx

2003-01-22 Priority to CN03802699.6A priority patent/CN1279089C/zh

2003-01-22 Priority to JP2003562180A priority patent/JP4462934B2/ja

2003-01-22 Priority to PCT/SE2003/000117 priority patent/WO2003062306A1/en

2003-01-22 Priority to HK05103304.0A priority patent/HK1070667B/en

2003-01-22 Priority to US10/501,024 priority patent/US7091308B2/en

2003-01-22 Priority to EP03731877A priority patent/EP1468040B1/en

2003-07-26 Publication of SE0200207L publication Critical patent/SE0200207L/

2004-08-10 Publication of SE524461C2 publication Critical patent/SE524461C2/sv

Links

229920000570 polyether Polymers 0.000 title claims abstract description 79
239000004721 Polyphenylene oxide Substances 0.000 title claims abstract description 65
239000000203 mixture Substances 0.000 title claims description 25
229920000642 polymer Polymers 0.000 claims abstract description 37
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 24
125000002947 alkylene group Chemical group 0.000 claims abstract description 15
AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 claims description 26
239000002253 acid Substances 0.000 claims description 21
235000014113 dietary fatty acids Nutrition 0.000 claims description 21
229930195729 fatty acid Natural products 0.000 claims description 21
239000000194 fatty acid Substances 0.000 claims description 21
150000004665 fatty acids Chemical class 0.000 claims description 20
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 16
229920000180 alkyd Polymers 0.000 claims description 16
238000006243 chemical reaction Methods 0.000 claims description 16
239000000839 emulsion Substances 0.000 claims description 16
-1 ditrimethylolethane Chemical compound 0.000 claims description 15
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 14
239000000049 pigment Substances 0.000 claims description 13
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 12
238000000576 coating method Methods 0.000 claims description 12
150000008064 anhydrides Chemical class 0.000 claims description 9
239000006185 dispersion Substances 0.000 claims description 8
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 8
229920005989 resin Polymers 0.000 claims description 8
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UNMJLQGKEDTEKJ-UHFFFAOYSA-N (3-ethyloxetan-3-yl)methanol Chemical compound CCC1(CO)COC1 UNMJLQGKEDTEKJ-UHFFFAOYSA-N 0.000 claims description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical group OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 6
239000007795 chemical reaction product Substances 0.000 claims description 6
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 6
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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 5
FZIIBDOXPQOKBP-UHFFFAOYSA-N 2-methyloxetane Chemical compound CC1CCO1 FZIIBDOXPQOKBP-UHFFFAOYSA-N 0.000 claims description 5
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ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 5
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125000001931 aliphatic group Chemical group 0.000 claims description 5
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ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 claims description 5
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239000000539 dimer Substances 0.000 claims description 5
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UCAOGXRUJFKQAP-UHFFFAOYSA-N n,n-dimethyl-5-nitropyridin-2-amine Chemical compound CN(C)C1=CC=C([N+]([O-])=O)C=N1 UCAOGXRUJFKQAP-UHFFFAOYSA-N 0.000 claims description 5
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239000013638 trimer Substances 0.000 claims description 5
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims description 5
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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 claims description 4
235000003222 Helianthus annuus Nutrition 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
239000004568 cement Substances 0.000 claims description 4
GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims description 4
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 claims description 4
150000004820 halides Chemical class 0.000 claims description 4
125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 4
FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims description 4
239000004848 polyfunctional curative Substances 0.000 claims description 4
239000003760 tallow Substances 0.000 claims description 4
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 4
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 claims description 3
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 3
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 3
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 3
WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 3
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 3
239000005642 Oleic acid Substances 0.000 claims description 3
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 3
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims description 3
229920001807 Urea-formaldehyde Polymers 0.000 claims description 3
ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 claims description 3
XDODWINGEHBYRT-UHFFFAOYSA-N [2-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCCC1CO XDODWINGEHBYRT-UHFFFAOYSA-N 0.000 claims description 3
ZTISUHQLYYPYFA-UHFFFAOYSA-N [5-(hydroxymethyl)-1,3-dioxan-5-yl]methanol Chemical compound OCC1(CO)COCOC1 ZTISUHQLYYPYFA-UHFFFAOYSA-N 0.000 claims description 3
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 3
125000005442 diisocyanate group Chemical group 0.000 claims description 3
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 3
239000000976 ink Substances 0.000 claims description 3
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229920005862 polyol Polymers 0.000 claims description 3
150000003077 polyols Chemical class 0.000 claims description 3
239000000600 sorbitol Substances 0.000 claims description 3
229920001187 thermosetting polymer Polymers 0.000 claims description 3
229920006305 unsaturated polyester Polymers 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
150000003923 2,5-pyrrolediones Chemical class 0.000 claims description 2
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 claims description 2
AWQSAIIDOMEEOD-UHFFFAOYSA-N 5,5-Dimethyl-4-(3-oxobutyl)dihydro-2(3H)-furanone Chemical compound CC(=O)CCC1CC(=O)OC1(C)C AWQSAIIDOMEEOD-UHFFFAOYSA-N 0.000 claims description 2
XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 claims description 2
BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 claims description 2
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 2
235000021357 Behenic acid Nutrition 0.000 claims description 2
239000005711 Benzoic acid Substances 0.000 claims description 2
DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 2
239000005632 Capric acid (CAS 334-48-5) Substances 0.000 claims description 2
239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 claims description 2
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 2
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BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 claims description 2
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OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
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WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
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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
- C08G65/26—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 and other compounds
- C08G65/2603—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 and other compounds the other compounds containing oxygen
- C08G65/2606—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 and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—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 and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyethers (AREA)
Paints Or Removers (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Adhesives Or Adhesive Processes (AREA)

SE0200207A 2002-01-25 2002-01-25 Kedjeförlängd dendritisk polyeter, komposition samt användning därav SE524461C2 (sv)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
SE0200207A SE524461C2 (sv)	2002-01-25	2002-01-25	Kedjeförlängd dendritisk polyeter, komposition samt användning därav
CN03802699.6A CN1279089C (zh)	2002-01-25	2003-01-22	链伸长树枝状聚醚
JP2003562180A JP4462934B2 (ja)	2002-01-25	2003-01-22	連鎖延長樹枝状ポリエーテル
PCT/SE2003/000117 WO2003062306A1 (en)	2002-01-25	2003-01-22	Chain extended dendritic polyether
HK05103304.0A HK1070667B (en)	2002-01-25	2003-01-22	Chain extended dendritic polyether
US10/501,024 US7091308B2 (en)	2002-01-25	2003-01-22	Chain extended dendritic polyether
EP03731877A EP1468040B1 (en)	2002-01-25	2003-01-22	Chain extended dendritic polyether

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE0200207A SE524461C2 (sv)	2002-01-25	2002-01-25	Kedjeförlängd dendritisk polyeter, komposition samt användning därav

Publications (3)

Publication Number	Publication Date
SE0200207D0 SE0200207D0 (sv)	2002-01-25
SE0200207L SE0200207L (sv)	2003-07-26
SE524461C2 true SE524461C2 (sv)	2004-08-10

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US (1)	US7091308B2 ( )
EP (1)	EP1468040B1 ( )
JP (1)	JP4462934B2 ( )
CN (1)	CN1279089C ( )
SE (1)	SE524461C2 ( )
WO (1)	WO2003062306A1 ( )

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KR100578737B1 (ko) *	2003-06-25	2006-05-12	학교법인 포항공과대학교	반응성 방사구조 고분자 및 이를 이용한 저유전성 고분자복합체 박막
DE10329723B3 (de) *	2003-07-02	2004-12-02	Clariant Gmbh	Alkoxylierte Dendrimere und ihre Verwendung als biologisch abbaubare Emulsionsspalter
CN1309752C (zh) *	2003-09-29	2007-04-11	中国科学院理化技术研究所	聚醚树枝体疏水缔合丙烯酰胺共聚物及其合成方法
SE526994C2 (sv) *	2003-11-12	2005-12-06	Perstorp Specialty Chem Ab	Strålningshärdande vattenburen komposition
US7507785B2 (en) *	2004-07-15	2009-03-24	Agfa Graphics N.V.	Polymeric co-initiators
EP1616897B1 (en) *	2004-07-15	2010-03-31	Agfa Graphics N.V.	Novel polymeric co-initiators
ATE382329T1 (de) *	2004-08-17	2008-01-15	Unilever Nv	Verfahren zur haarbehandlung mit einer zusammensetzung enthaltend ein dentritisches polymer
JP2009514995A (ja) *	2005-11-03	2009-04-09	ピーターソン，リリアン	高リノレン酸亜麻仁油組成物
ATE546496T1 (de)	2006-05-23	2012-03-15	Basf Se	Verwendung von hyperverzweigten polycarbonaten als dispergiermittel für pigmente
KR101066896B1 (ko) *	2006-06-20	2011-09-27	디아이씨 가부시끼가이샤	다분기 폴리에테르폴리올 및 우레탄계 수지 조성물
US8409715B2 (en)	2006-09-29	2013-04-02	Dic Corporation	Cation-polymerizable resin composition containing multi-branched polyether polyol, adhesive agent comprising the composition, and laminate and polarizing plate using the adhesive agent
CN101589111B (zh) *	2006-12-12	2012-09-19	西巴控股有限公司	包含树枝状聚合物的阻燃组合物
US8206827B2 (en) *	2007-03-15	2012-06-26	Nanovere Technologies, Llc	Dendritic polyurethane coating
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US7091308B2 (en)	2006-08-15
US20050131205A1 (en)	2005-06-16
EP1468040B1 (en)	2012-06-13
JP4462934B2 (ja)	2010-05-12
HK1070667A1 (en)	2005-06-24
CN1279089C (zh)	2006-10-11
SE0200207L (sv)	2003-07-26
WO2003062306A1 (en)	2003-07-31
SE0200207D0 (sv)	2002-01-25
EP1468040A1 (en)	2004-10-20
JP2005515283A (ja)	2005-05-26
CN1622968A (zh)	2005-06-01

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