PL420247A1 - Method for oxidation of limonene - Google Patents

Method for oxidation of limonene

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Publication number
PL420247A1
PL420247A1 PL420247A PL42024717A PL420247A1 PL 420247 A1 PL420247 A1 PL 420247A1 PL 420247 A PL420247 A PL 420247A PL 42024717 A PL42024717 A PL 42024717A PL 420247 A1 PL420247 A1 PL 420247A1
Authority
PL
Poland
Prior art keywords
limonene
oxidation
inert gas
activated carbon
catalyst
Prior art date
Application number
PL420247A
Other languages
Polish (pl)
Other versions
PL231108B1 (en
Inventor
Agnieszka Wróblewska
Beata Michalkiewicz
Jarosław Serafin
Jacek Młodzik
Alicja Gawarecka
Piotr Miądlicki
Zbigniew Czech
Adrian Krzysztof Antosik
Katarzyna Wilpiszewska
Original Assignee
Zachodniopomorski Uniwersytet Technologiczny W Szczecinie
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 Zachodniopomorski Uniwersytet Technologiczny W Szczecinie filed Critical Zachodniopomorski Uniwersytet Technologiczny W Szczecinie
Priority to PL420247A priority Critical patent/PL231108B1/en
Publication of PL420247A1 publication Critical patent/PL420247A1/en
Publication of PL231108B1 publication Critical patent/PL231108B1/en

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  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Przedmiotem zgłoszenia jest sposób utleniania limonenu, za pomocą 60% roztworu wodnego nadtlenku wodoru, w obecności katalizatora w postaci węgla aktywnego i metanolu jako rozpuszczalnika, który charakteryzuje się tym, że jako katalizator stosuje się węgiel aktywny w ilości 4% wagowych w mieszaninie reakcyjnej, otrzymany ze zmieszania folii na bazie karboksymetyloskrobi z wodnym roztworem KOH jako aktywatorem, przy stosunku wagowym karboksymetyloskrobi do aktywatora 1 : 0,25 - 5, pozostawieniu mieszaniny na czas 0 - 24 godziny w celu impregnacji, następnie suszeniu otrzymanej mieszaniny, jej karbonizacji w temperaturze 400 - 1000°C, w atmosferze gazu obojętnego chemicznie, przemywaniu i suszeniu. Proces utleniania limonenu prowadzi się w temperaturach 80 - 120°C, w czasie 6 godzin, przy stosunku molowym limonen : utleniacz = 1 : 2, przy stężeniu metanolu w mieszanie reakcyjnej wynoszącym 70% wagowych. Utlenianie prowadzi się pod ciśnieniem autogenicznym w autoklawie wyposażonym we wkładkę teflonową. Surowce w procesie utleniania wprowadza się w następującej kolejności: katalizator, metanol, limonen i na końcu utleniacz. Podczas utleniania stosuje się intensywność mieszania wynoszącą 500 obrotów/minutę .Podczas otrzymywania węgla aktywnego po ochłodzeniu, po karbonizacji otrzymany produkt przemywa się wodą destylowaną do odczynu obojętnego, traktuje kwasem solnym i ponownie przemywa wodą destylowaną do odczynu obojętnego i tak otrzymany węgiel aktywny suszy się. Gaz obojętny chemicznie w procesie karbonizacji podaje się z prędkością 0,5 - 50 l/h. Jako gaz obojętny chemicznie stosuje się azot lub dowolny gaz szlachetny.The subject of the application is a method of oxidizing limonene with a 60% aqueous solution of hydrogen peroxide in the presence of a catalyst in the form of activated carbon and methanol as a solvent, which is characterized in that the catalyst used is 4% by weight of active carbon in the reaction mixture, obtained from mixing carboxymethyl starch based film with an aqueous KOH solution as activator, with a carboxymethyl starch / activator weight ratio of 1: 0.25-5, allowing the mixture to remain for 0-24 hours for impregnation, then drying the resulting mixture, and carbonizing it at 400 - 1000 ° C, in an inert gas atmosphere, washing and drying. The oxidation of limonene is carried out at temperatures of 80-120 ° C for 6 hours, with a molar ratio of limonene: oxidant = 1: 2, with a methanol concentration of 70% by weight in the reaction mixture. Oxidation is carried out under autogenic pressure in an autoclave equipped with a Teflon liner. The raw materials in the oxidation process are introduced in the following order: catalyst, methanol, limonene and finally the oxidant. During the oxidation, a stirring intensity of 500 rpm is used. During the preparation of activated carbon after cooling, after carbonization the product obtained is washed with distilled water to neutral, treated with hydrochloric acid and washed again with distilled water to neutral, and the activated carbon is dried. Chemically inert gas in the carbonization process is fed at a speed of 0.5 - 50 l / h. Nitrogen or any noble gas is used as chemically inert gas.

PL420247A 2017-01-19 2017-01-19 Method for oxidation of limonene PL231108B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL420247A PL231108B1 (en) 2017-01-19 2017-01-19 Method for oxidation of limonene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL420247A PL231108B1 (en) 2017-01-19 2017-01-19 Method for oxidation of limonene

Publications (2)

Publication Number Publication Date
PL420247A1 true PL420247A1 (en) 2018-07-30
PL231108B1 PL231108B1 (en) 2019-01-31

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Family Applications (1)

Application Number Title Priority Date Filing Date
PL420247A PL231108B1 (en) 2017-01-19 2017-01-19 Method for oxidation of limonene

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PL (1) PL231108B1 (en)

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Publication number Publication date
PL231108B1 (en) 2019-01-31

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