DD146709A5 - Verfahren zur herstellung von vernetzten polyaetheresterharzen - Google Patents

Verfahren zur herstellung von vernetzten polyaetheresterharzen Download PDF

Info

Publication number: DD146709A5
Authority: DD; German Democratic Republic
Prior art keywords: glycol; hydroxy; resins; ether; oligo
Prior art date: 1978-10-20

Application number

DD79216319A

Other languages

German (de)

English (en)

Inventor

Zbigniew Jedlinski

Bogdan Thomalla

Antoni Kotas

Stanislaw Jedlinski

Wladyslaw Pilat

Jan Jach

Original Assignee

Polska Akademia Nauk Zaklad

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.)

1978-10-20

Filing date

1979-10-18

Publication date

1981-02-25

1979-10-18 Application filed by Polska Akademia Nauk Zaklad filed Critical Polska Akademia Nauk Zaklad

1981-02-25 Publication of DD146709A5 publication Critical patent/DD146709A5/de

Links

229920005989 resin Polymers 0.000 title claims abstract description 24
239000011347 resin Substances 0.000 title claims abstract description 24
238000004519 manufacturing process Methods 0.000 title 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 31
JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 claims abstract description 12
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 11
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 11
238000004132 cross linking Methods 0.000 claims abstract description 10
150000002334 glycols Chemical class 0.000 claims abstract description 8
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 8
238000006068 polycondensation reaction Methods 0.000 claims abstract description 8
238000002360 preparation method Methods 0.000 claims abstract description 7
229950011260 betanaphthol Drugs 0.000 claims abstract description 6
150000001875 compounds Chemical class 0.000 claims abstract description 6
239000000203 mixture Substances 0.000 claims abstract description 5
239000000178 monomer Substances 0.000 claims abstract description 5
150000008064 anhydrides Chemical class 0.000 claims abstract description 4
238000007334 copolymerization reaction Methods 0.000 claims abstract description 3
238000000034 method Methods 0.000 claims description 12
239000002253 acid Substances 0.000 claims description 8
239000004721 Polyphenylene oxide Substances 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
229920000570 polyether Polymers 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 abstract description 3
239000000126 substance Substances 0.000 abstract description 3
150000001991 dicarboxylic acids Chemical class 0.000 abstract description 2
101100072620 Streptomyces griseus ind2 gene Proteins 0.000 abstract 3
-1 ethylene, propylene Chemical group 0.000 abstract 1
238000006243 chemical reaction Methods 0.000 description 6
241000428199 Mustelinae Species 0.000 description 5
238000005452 bending Methods 0.000 description 5
229920000728 polyester Polymers 0.000 description 5
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
229920001225 polyester resin Polymers 0.000 description 4
239000004645 polyester resin Substances 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
235000011037 adipic acid Nutrition 0.000 description 2
239000001361 adipic acid Substances 0.000 description 2
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
229920006305 unsaturated polyester Polymers 0.000 description 1
229920006337 unsaturated polyester resin Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/676—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyesters Or Polycarbonates (AREA)
Macromonomer-Based Addition Polymer (AREA)

DD79216319A 1978-10-20 1979-10-18 Verfahren zur herstellung von vernetzten polyaetheresterharzen DD146709A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
PL1978210406A PL117785B1 (en)	1978-10-20	1978-10-20	Method of manufacture of cross-linked polyetherester resinsykh smol

Publications (1)

Publication Number	Publication Date
DD146709A5 true DD146709A5 (de)	1981-02-25

Family

ID=19992135

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79216319A DD146709A5 (de)	1978-10-20	1979-10-18	Verfahren zur herstellung von vernetzten polyaetheresterharzen

Country Status (6)

Country	Link
US (1)	US4293685A (pl)
DD (1)	DD146709A5 (pl)
DE (1)	DE2942425A1 (pl)
FR (1)	FR2439213A1 (pl)
IT (1)	IT1125531B (pl)
PL (1)	PL117785B1 (pl)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2010016555A1 (ja) *	2008-08-07	2010-02-11	三菱化学株式会社	重合体、発光層材料、有機電界発光素子材料、有機電界発光素子用組成物、これらを利用した有機電界発光素子、太陽電池素子、有機ｅｌ表示装置、及び有機ｅｌ照明

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3838106A (en) *	1972-07-20	1974-09-24	Standard Oil Co	Manufacture of unsaturated polyesters
US3923928A (en) *	1973-01-31	1975-12-02	Union Carbide Corp	Unsaturated polyesters and compositions based thereon
US4115362A (en) *	1975-10-03	1978-09-19	Teijin Limited	Process for preparing polyesters
PL110678B1 (en) *	1977-09-02	1980-07-31	Zaklad Polimerow Pan	Method of producing unsaturated polyester resins with regular structure of lattice

1978
- 1978-10-20 PL PL1978210406A patent/PL117785B1/pl unknown
1979
- 1979-10-16 FR FR7925699A patent/FR2439213A1/fr not_active Withdrawn
- 1979-10-18 DD DD79216319A patent/DD146709A5/de unknown
- 1979-10-19 DE DE19792942425 patent/DE2942425A1/de not_active Ceased
- 1979-10-19 IT IT26667/79A patent/IT1125531B/it active
- 1979-10-25 US US06/088,278 patent/US4293685A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
IT1125531B (it)	1986-05-14
PL117785B1 (en)	1981-08-31
FR2439213A1 (fr)	1980-05-16
IT7926667A0 (it)	1979-10-19
DE2942425A1 (de)	1980-04-24
PL210406A1 (pl)	1980-05-19
US4293685A (en)	1981-10-06

Publication	Publication Date	Title
EP0126341B1 (de)	1989-02-01	Verfahren zur Herstellung von (Meth)-acrylsäureestern und deren Verwendung
DE69529574T2 (de)	2003-08-21	Hyperverzweigtes makromolekül vom typ polyester
CH621564A5 (pl)	1981-02-13
EP1492834A1 (de)	2005-01-05	Ungesättigte, amorphe polyester auf basis bestimmter dicidolisomerer und gesättigter dicarbonsäuren
EP0124070B1 (de)	1989-04-05	Verfahren zur Herstellung von Polyester- oder Polyether-polyester-polyolen
DE1168632B (de)	1964-04-23	Verfahren zur Herstellung von Formkoerpern auf Aminoplastbasis
DE2052961C3 (de)	1980-10-16	Mischpolymerisierbare Massen und Verfahren zu ihrer Herstellung
DE10261006A1 (de)	2004-07-08	Dispersionen amorpher, ungesättigter Polyesterharze auf Basis bestimmter Dicidolisomerer
DE69230795T2 (de)	2000-08-03	Vernetzungsmittel und vernetzbare zusammensetzung
DE19524812A1 (de)	1997-01-09	Strahlungshärtbare Acrylate mit eingebautem Photoinitiatoren
DE1268297B (de)	1968-05-16	Verwendung von Alkydharzen als Filmbildner in Lacken
EP0194434A1 (de)	1986-09-17	Polymerisierbare, Hydroxylgruppen tragende Carbamoyloxyalkyldicarbonsäureester, Verfahren zu ihrer Herstellung und ihrer Verwendung
DD146709A5 (de)	1981-02-25	Verfahren zur herstellung von vernetzten polyaetheresterharzen
EP0664817B1 (de)	2000-04-26	Hilfsmittel zur verarbeitung von kunststoffen, verfahren zur herstellung von diesem hilfsmittel und verfahren zur herstellung von reduzierte monomeremission aufweisendem polyesterharz
DE2166449B2 (de)	1980-01-03	Härtbare Mischung aus polymerisierbaren Verbindungen
DE2922377C2 (de)	1982-08-26	Pulverförmige Überzugsmittel und Anstrichmittel
EP0902066B1 (de)	2003-05-07	Härtbare Beschichtungen aus oligomeren Kondensationsprodukten
DE1769432A1 (de)	1971-09-16	Zweikomponenten-UEberzugsmassen auf Polyurethanbasis
DE2547124C2 (de)	1982-05-06	Wärmehärtbare Harzzusammensetzungen
AT229040B (de)	1963-08-26	Verfahren zur Herstellung von hochmolekularen Polyestern
DE10223313A1 (de)	2003-12-11	Modifizierte Epoxyacrylate
DE2218364A1 (de)	1972-11-02	Ungesättigte Polyester-Harzmassen
DE2041252A1 (de)	1971-03-25	Neue Polyesterharze des aethylenisch ungesaettigten Typs
DE19922032A1 (de)	2000-11-16	Verfahren zur Herstellung von bei Raumtemperatur festen, modifizierten cycloaliphatischen Epoxidharzen und ihre Verwendung
DE1520747C (de)		Verfahren zur Herstellung von Alkydharzen