PL400931A1 - Method for preparing poly (ester-carbonates) by non-phosgene method - Google Patents

Method for preparing poly (ester-carbonates) by non-phosgene method

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Publication number
PL400931A1
PL400931A1 PL400931A PL40093112A PL400931A1 PL 400931 A1 PL400931 A1 PL 400931A1 PL 400931 A PL400931 A PL 400931A PL 40093112 A PL40093112 A PL 40093112A PL 400931 A1 PL400931 A1 PL 400931A1
Authority
PL
Poland
Prior art keywords
ester
carbonates
diol
mixture
temperature
Prior art date
Application number
PL400931A
Other languages
Polish (pl)
Other versions
PL219394B1 (en
Inventor
Gabriel Rokicki
Magdalena Mazurek
Karolina Tomczyk
Tomasz Bruliński
Paweł Parzuchowski
Zbigniew Florjańczyk
Original Assignee
Politechnika Warszawska
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.)
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Publication date
Application filed by Politechnika Warszawska filed Critical Politechnika Warszawska
Priority to PL400931A priority Critical patent/PL219394B1/en
Publication of PL400931A1 publication Critical patent/PL400931A1/en
Publication of PL219394B1 publication Critical patent/PL219394B1/en

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Abstract

Sposób wytwarzania poli(estro-węglanów) polega na tym, że węglan dimetylu poddaje się reakcji z α,ω-diolem, w obecności katalizatora transestryfikacji, przy czym stosuje się 7-10-krotny nadmiar molowy węglanu di metylu. Otrzymany bis(metylowęglan)alkilenu poddaje się reakcji z estrem dimetylowym lub dietylowym kwasu dikarboksylowego lub ich mieszaniną w stosunku molowym od 1:9,5 do 9,5:1 i α,ω-diolem w stosunku molowym od 1,5:1-2:1 do sumy moli obu składników kwasowych, przy czym reakcję polikondensacji prowadzi się najpierw w temperaturze 150-200°C, w przepływie azotu pod normalnym ciśnieniem, a następnie po odebraniu powyżej 95% teoretycznej ilości metanolu lub etanolu lub ich mieszaniny, pod zmniejszonym ciśnieniem w temperaturze nieprzekraczającej 220°C.The method of producing poly(ester-carbonates) consists in reacting dimethyl carbonate with α,ω-diol in the presence of a transesterification catalyst, wherein a 7-10-fold molar excess of dimethyl carbonate is used. The obtained alkylene bis(methylcarbonate) is reacted with a dimethyl or diethyl ester of a dicarboxylic acid or a mixture thereof in a molar ratio of 1:9.5 to 9.5:1 and α,ω-diol in a molar ratio of 1.5:1-2:1 to the sum of moles of both acid components, wherein the polycondensation reaction is carried out first at a temperature of 150-200°C, in a nitrogen flow at normal pressure, and then after removing more than 95% of the theoretical amount of methanol or ethanol or their mixture, under reduced pressure at a temperature not exceeding 220°C.

PL400931A 2012-09-26 2012-09-26 Method for preparing poly (ester-carbonates) by non-phosgene method PL219394B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL400931A PL219394B1 (en) 2012-09-26 2012-09-26 Method for preparing poly (ester-carbonates) by non-phosgene method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL400931A PL219394B1 (en) 2012-09-26 2012-09-26 Method for preparing poly (ester-carbonates) by non-phosgene method

Publications (2)

Publication Number Publication Date
PL400931A1 true PL400931A1 (en) 2014-03-31
PL219394B1 PL219394B1 (en) 2015-04-30

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ID=50350312

Family Applications (1)

Application Number Title Priority Date Filing Date
PL400931A PL219394B1 (en) 2012-09-26 2012-09-26 Method for preparing poly (ester-carbonates) by non-phosgene method

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PL (1) PL219394B1 (en)

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Publication number Publication date
PL219394B1 (en) 2015-04-30

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