DD292468A5 - Verfahren zur polymerisation von epoxidverbindungen - Google Patents

Verfahren zur polymerisation von epoxidverbindungen Download PDF

Info

Publication number: DD292468A5
Authority: DD; German Democratic Republic
Prior art keywords: polymerization; compound; lewis base; acidic; epoxide
Prior art date: 1990-03-09

Application number

DD90338526A

Other languages

German (de)

English (en)

Inventor

Axel Boettcher

Klaus Dathe

Manfred Fedtke

Manfred Doering

Egon Uhlig

Bernd Nestler

Original Assignee

Zeiss Carl Jena Gmbh

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.)

1990-03-09

Filing date

1990-03-09

Publication date

1991-08-01

1990-03-09 Application filed by Zeiss Carl Jena Gmbh filed Critical Zeiss Carl Jena Gmbh

1990-03-09 Priority to DD90338526A priority Critical patent/DD292468A5/de

1991-03-06 Priority to SU915010651A priority patent/RU2086572C1/ru

1991-03-06 Priority to FI915291A priority patent/FI915291A7/fi

1991-03-06 Priority to ES91905067T priority patent/ES2036162T3/es

1991-03-06 Priority to AT91905067T priority patent/ATE119174T1/de

1991-03-06 Priority to EP91905067A priority patent/EP0518908B1/de

1991-03-06 Priority to DE59104812T priority patent/DE59104812D1/de

1991-03-06 Priority to KR1019910701562A priority patent/KR970001539B1/ko

1991-03-06 Priority to BR919104778A priority patent/BR9104778A/pt

1991-03-06 Priority to JP50518291A priority patent/JP3215106B2/ja

1991-03-06 Priority to PCT/EP1991/000419 priority patent/WO1991013925A1/de

1991-03-06 Priority to CA002054212A priority patent/CA2054212C/en

1991-08-01 Publication of DD292468A5 publication Critical patent/DD292468A5/de

1991-11-08 Priority to NO91914377A priority patent/NO914377L/no

1992-09-29 Priority to LVP-92-135A priority patent/LV10116B/lv

1992-10-02 Priority to LTIP217A priority patent/LT3106B/lt

1993-03-16 Priority to GR920300130T priority patent/GR920300130T1/el

1994-03-02 Priority to US08/204,782 priority patent/US5395913A/en

1994-09-27 Priority to US08/313,721 priority patent/US5525698A/en

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 15
238000000034 method Methods 0.000 title claims abstract description 13
239000004593 Epoxy Substances 0.000 title abstract description 11
230000000379 polymerizing effect Effects 0.000 title 1
238000006116 polymerization reaction Methods 0.000 claims abstract description 25
239000002879 Lewis base Substances 0.000 claims abstract description 22
-1 epoxide compounds Chemical class 0.000 claims abstract description 22
150000007527 lewis bases Chemical class 0.000 claims abstract description 22
238000006243 chemical reaction Methods 0.000 claims abstract description 10
230000008569 process Effects 0.000 claims abstract description 4
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 14
239000003446 ligand Substances 0.000 claims description 10
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
239000013522 chelant Substances 0.000 claims description 4
229910052739 hydrogen Chemical group 0.000 claims description 4
239000001257 hydrogen Chemical group 0.000 claims description 4
229910052751 metal Inorganic materials 0.000 claims description 4
239000002184 metal Substances 0.000 claims description 4
229910021645 metal ion Inorganic materials 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
125000004437 phosphorous atom Chemical group 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
150000004696 coordination complex Chemical group 0.000 claims description 2
125000003700 epoxy group Chemical group 0.000 claims description 2
150000002576 ketones Chemical class 0.000 claims description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
150000003568 thioethers Chemical class 0.000 claims 1
230000000977 initiatory effect Effects 0.000 abstract description 3
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract 2
APRRQJCCBSJQOQ-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S(O)(=O)=O)=CC2=C1 APRRQJCCBSJQOQ-UHFFFAOYSA-N 0.000 abstract 1
229940106691 bisphenol a Drugs 0.000 abstract 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
239000000203 mixture Substances 0.000 description 13
239000000654 additive Substances 0.000 description 8
239000000853 adhesive Substances 0.000 description 7
230000001070 adhesive effect Effects 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
150000002460 imidazoles Chemical class 0.000 description 6
239000003822 epoxy resin Substances 0.000 description 5
229920000647 polyepoxide Polymers 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
229910017052 cobalt Inorganic materials 0.000 description 4
239000010941 cobalt Substances 0.000 description 4
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
ZYUVGYBAPZYKSA-UHFFFAOYSA-N 5-(3-hydroxybutan-2-yl)-4-methylbenzene-1,3-diol Chemical compound CC(O)C(C)C1=CC(O)=CC(O)=C1C ZYUVGYBAPZYKSA-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
239000002585 base Substances 0.000 description 3
230000008901 benefit Effects 0.000 description 3
NHADDZMCASKINP-HTRCEHHLSA-N decarboxydihydrocitrinin Natural products C1=C(O)C(C)=C2[C@H](C)[C@@H](C)OCC2=C1O NHADDZMCASKINP-HTRCEHHLSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000463 material Substances 0.000 description 3
230000007246 mechanism Effects 0.000 description 3
238000000465 moulding Methods 0.000 description 3
150000002924 oxiranes Chemical class 0.000 description 3
239000004848 polyfunctional curative Substances 0.000 description 3
150000003573 thiols Chemical class 0.000 description 3
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
230000001133 acceleration Effects 0.000 description 2
125000005595 acetylacetonate group Chemical group 0.000 description 2
239000002253 acid Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
235000015895 biscuits Nutrition 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000003999 initiator Substances 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
229920002959 polymer blend Polymers 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
231100000331 toxic Toxicity 0.000 description 2
230000002588 toxic effect Effects 0.000 description 2
241000557248 Argia lugens Species 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
240000002024 Gossypium herbaceum Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000009471 action Effects 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
150000004697 chelate complex Chemical class 0.000 description 1
MJSNUBOCVAKFIJ-LNTINUHCSA-N chromium;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Cr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O MJSNUBOCVAKFIJ-LNTINUHCSA-N 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000000536 complexating effect Effects 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
229920001795 coordination polymer Polymers 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000003814 drug Substances 0.000 description 1
238000004870 electrical engineering Methods 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000004849 latent hardener Substances 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
230000002028 premature Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
239000012779 reinforcing material Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
238000003385 ring cleavage reaction Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000007017 scission Effects 0.000 description 1
238000007669 thermal treatment Methods 0.000 description 1
238000002411 thermogravimetry Methods 0.000 description 1

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Epoxy Resins (AREA)

DD90338526A 1990-03-09 1990-03-09 Verfahren zur polymerisation von epoxidverbindungen DD292468A5 (de)

Priority Applications (18)

Application Number	Priority Date	Filing Date	Title
DD90338526A DD292468A5 (de)	1990-03-09	1990-03-09	Verfahren zur polymerisation von epoxidverbindungen
JP50518291A JP3215106B2 (ja)	1990-03-09	1991-03-06	エポキシド化合物の重合方法
PCT/EP1991/000419 WO1991013925A1 (de)	1990-03-09	1991-03-06	Verfahren zur polymerisation von epoxidverbindungen
ES91905067T ES2036162T3 (es)	1990-03-09	1991-03-06	Procedimiento para la polimerizacion de compuestos epoxidicos.
AT91905067T ATE119174T1 (de)	1990-03-09	1991-03-06	Verfahren zur polymerisation von epoxidverbindungen.
EP91905067A EP0518908B1 (de)	1990-03-09	1991-03-06	Verfahren zur polymerisation von epoxidverbindungen
DE59104812T DE59104812D1 (de)	1990-03-09	1991-03-06	Verfahren zur polymerisation von epoxidverbindungen.
KR1019910701562A KR970001539B1 (ko)	1990-03-09	1991-03-06	에폭시드 화합물의 중합 방법
BR919104778A BR9104778A (pt)	1990-03-09	1991-03-06	Processo para a polimerizacao de compostos de epoxido
SU915010651A RU2086572C1 (ru)	1990-03-09	1991-03-06	Способ полимеризации эпоксисоединений, смесь эпоксисоединений, клеющая и уплотняющая масса, связующее
FI915291A FI915291A7 (fi)	1990-03-09	1991-03-06	Menetelmä epoksidiyhdisteiden polymeroimiseksi
CA002054212A CA2054212C (en)	1990-03-09	1991-03-06	Method for polymerization of epoxide compounds
NO91914377A NO914377L (no)	1990-03-09	1991-11-08	Fremgangsmaate for polymerisering av epoksidforbindelser
LVP-92-135A LV10116B (en)	1990-03-09	1992-09-29	Method of polimerisation of epoxy compounds
LTIP217A LT3106B (en)	1990-03-09	1992-10-02	Process for the polymerisation of epoxycompounds
GR920300130T GR920300130T1 (en)	1990-03-09	1993-03-16	Method for polymerization of epoxide compounds.
US08/204,782 US5395913A (en)	1990-03-09	1994-03-02	Polymerizable epoxide mixtures and process using Lewis base complexes
US08/313,721 US5525698A (en)	1990-03-09	1994-09-27	Polymerizable epoxide mixtures and process

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DD90338526A DD292468A5 (de)	1990-03-09	1990-03-09	Verfahren zur polymerisation von epoxidverbindungen

Publications (1)

Publication Number	Publication Date
DD292468A5 true DD292468A5 (de)	1991-08-01

Family

ID=5616937

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD90338526A DD292468A5 (de)	1990-03-09	1990-03-09	Verfahren zur polymerisation von epoxidverbindungen

Country Status (2)

Country	Link
DD (1)	DD292468A5 (lt)
LT (1)	LT3106B (lt)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4231680A1 (de) *	1992-09-22	1994-03-24	Ruetgerswerke Ag	Verfahren zur Herstellung von Metallkomplexen mit hoher Koordinationszahl und deren Verwendung

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US355166A (en)		1886-12-28		Separator for steam-generators
CH269230A (it)	1948-08-13	1950-06-30	Benaglio Osvaldo	Quadrante per orologi da polso e da tasca.
US3310602A (en)	1962-07-26	1967-03-21	Borden Co	Curing epoxide resins with aromatic amine-aldehyde coordination complexes
US3367913A (en)	1966-09-09	1968-02-06	Interchem Corp	Thermosetting epoxy resin composition containing a zinc chelate
US3553166A (en)	1968-02-02	1971-01-05	Ppg Industries Inc	Mixtures of imidazole complexes and nitrogenous compound as curing agents for epoxy resins
US3624032A (en)	1969-04-24	1971-11-30	Morton Int Inc	Epoxy compositions cured with carboxylic acid anhydrides and metallic salt of acetylacetone
US3638007A (en)	1969-08-05	1972-01-25	Herbert B Brooks	Digital control simulator
US3635894A (en)	1969-11-06	1972-01-18	Ppg Industries Inc	Curable epoxy resin compositions containing organoimidazolium salt
US3642698A (en)	1970-05-15	1972-02-15	Air Prod & Chem	Epoxy resin curing with imidazole alkyl acid phosphate salt catalyst
US3632427A (en)	1970-05-15	1972-01-04	Air Prod & Chem	Epoxy resin and imidazole alkyl acid phosphate fiber treatment
US4105667A (en)	1970-07-17	1978-08-08	Minnesota Mining And Manufacturing Company	Imidazole type curing agents
US3746686A (en)	1971-07-12	1973-07-17	Shell Oil Co	Process for curing polyepoxides with polycarboxylic acid salts of an imidazole compound and compositions thereof
US3677978A (en)	1971-08-23	1972-07-18	Ppg Industries Inc	Metal salt complexes of imidazoles as curing agents for one-part epoxy resins
US3792016A (en)	1972-01-06	1974-02-12	Minnesota Mining & Mfg	Metal imidazolate-catalyzed systems
GB1435540A (en)	1972-07-06	1976-05-12	Mccall Corp	Curable solventless composition
US3956241A (en)	1974-06-07	1976-05-11	Aerojet-General Corporation	Latent catalysts for epoxy resins
US4137275A (en)	1976-04-27	1979-01-30	Westinghouse Electric Corp.	Latent accelerators for curing epoxy resins
US4159976A (en)	1977-03-10	1979-07-03	Loctite Corporation	Curable systems containing epoxy resin and methanol or ethanol solvent to suppress the catalytic reaction between epoxy resin and an imidazole catalytic curing agent
JPS53116391A (en)	1977-03-18	1978-10-11	Shikoku Kasei Kougiyou Kk	Novel imidazoleisocyanuric adduct synthesizing method thereof polyepoxy hardening method containing same as main component polyepoxy hardening method using same as hardening improver and method of pur
GB8304581D0 (en)	1983-02-18	1983-03-23	Secr Defence	Curing agents for epoxy resins
US4473674A (en)	1983-11-03	1984-09-25	The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration	Process for improving mechanical properties of epoxy resins by addition of cobalt ions

1990
- 1990-03-09 DD DD90338526A patent/DD292468A5/de not_active IP Right Cessation
1992
- 1992-10-02 LT LTIP217A patent/LT3106B/lt not_active IP Right Cessation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4231680A1 (de) *	1992-09-22	1994-03-24	Ruetgerswerke Ag	Verfahren zur Herstellung von Metallkomplexen mit hoher Koordinationszahl und deren Verwendung

Also Published As

Publication number	Publication date
LTIP217A (en)	1994-06-15
LT3106B (en)	1994-12-27

Legal Events

Date	Code	Title
1994-06-23	RPI	Change in the person, name or address of the patentee (searches according to art. 11 and 12 extension act)
1994-10-13	RPI	Change in the person, name or address of the patentee (searches according to art. 11 and 12 extension act)
1997-04-10	RPI	Change in the person, name or address of the patentee (searches according to art. 11 and 12 extension act)
1999-07-08	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0518908B1 (de)	1995-03-01	Verfahren zur polymerisation von epoxidverbindungen
DE3114677C2 (lt)	1993-09-23
DE1720998C2 (de)	1981-11-26	Verfahren zur Herstellung von Polybutadien mit einem hohen Gehalt an Vinylseitengruppen
EP0085836B1 (de)	1988-07-20	Verwendung polymerer Organo-Borverbindungen als Polymerisationsinitiatoren
US5525698A (en)	1996-06-11	Polymerizable epoxide mixtures and process
EP1125960B1 (de)	2005-05-11	Latente Kombinationsverbindungen und latente Ammoniumsalze aus Epoxidharzhärter und Flammschutzmittel sowie daraus hergestellte Epoxidharz-Systeme und -Produkte
DE2019816A1 (de)	1970-10-29	Formmassen aus Epoxyharzen
DE2421038B2 (de)	1978-01-05	Verfahren zur herstellung von hitzegehaerteten addukten aus siliciumwasserstoffverbindungen und trialkenylisocyanuraten, sowie zur herstellung hitzegehaerteter produkte daraus
DE19905448A1 (de)	2000-08-10	Cyanatharze und Epoxidverbindungen enthaltende härtbare Mischungen
DE3007684A1 (de)	1981-09-10	Hitzehaertbare zusammensetzungen
DE2623473C2 (de)	1985-05-09	Verwendung von Cumylphenol oder dessen Derivaten als Zusatz zu polymerisierbaren Zubereitungen auf der Basis von Epoxy-, Furan-, Phenol- oder Urethanharzen
DE69005819T2 (de)	1994-07-28	Thiolgruppen enthaltende polymerisation-co-katalysatoren.
DE1099162B (de)	1961-02-09	Verfahren zur Herstellung von Kunststoffen auf Grundlage von Polyepoxyden
EP0688804A2 (de)	1995-12-27	Mehrkomponentige, kationisch härtende Epoxidmassen sowie Verfahren zu ihrer Härtung
DE2811096A1 (de)	1979-02-08	Epoxyharzmasse
DD292468A5 (de)	1991-08-01	Verfahren zur polymerisation von epoxidverbindungen
EP0139110A1 (de)	1985-05-02	Härtbare Epoxidharze
DE1793138A1 (de)	1972-05-10	Verfahren zum Herstellen makrocyclischer Verbindungen und alicyclischer Ketone
DE1299427B (de)	1969-07-17	Verfahren zur Herstellung von Formkoerpern auf der Basis von Epoxvdpolyaddukten
DD293126A5 (de)	1991-08-22	Verfahren zur polymerisation von epoxidischen verbindungen
DE1158707B (de)	1963-12-05	Verfahren zum Haerten von Polyester-Formmassen, die Peroxyde und Vanadinverbindungen enthalten
EP0018948A2 (de)	1980-11-12	N-substituierte Asparaginsäurederivate, Verfahren zu ihrer Herstellung, ihre Verwendung und mit ihrer Hilfe hergestellte Epoxidharze
DE2854011C2 (de)	1983-04-21	Hitzehärtbare Masse und Verfahren zu deren Herstellung
DE68905175T2 (de)	1993-09-02	Verfahren zur stabilisierung von zyklischen carbonaten.
DE2853885A1 (de)	1979-06-21	Haertbare zusammensetzung und verfahren zum schaeumen derselben

DD292468A5 - Verfahren zur polymerisation von epoxidverbindungen - Google Patents

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Priority Applications (18)

Applications Claiming Priority (1)

Publications (1)

Family

ID=5616937

Family Applications (1)

Country Status (2)

Cited By (1)

Family Cites Families (21)

Cited By (1)

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