Одержання ацетацеталі пропіленгліколю на твердих кислотних каталізаторах

Formation of 2,4-dimethyl-1,3-dioxolane from propylene glycol and acetaldehyde over sulfonic cation-exchange resins and acidic oxides at 10–50°C has been studied . The highest cyclic acetal yield of 83% at 84% propylene glycol conversion was achieved over sulforesin KU-2.8.

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Bibliographische Detailangaben
Datum:2015
Hauptverfasser: Bondarenko, E. A., Sharanda, M. E., Brei, V. V.
Format: Artikel
Sprache:Ukrainian
Veröffentlicht: Chuiko Institute of Surface Chemistry National Academy of Sciences of Ukraine 2015
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Online Zugang:https://www.cpts.com.ua/index.php/cpts/article/view/356
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Назва журналу:Chemistry, Physics and Technology of Surface

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Chemistry, Physics and Technology of Surface
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Zusammenfassung:Formation of 2,4-dimethyl-1,3-dioxolane from propylene glycol and acetaldehyde over sulfonic cation-exchange resins and acidic oxides at 10–50°C has been studied . The highest cyclic acetal yield of 83% at 84% propylene glycol conversion was achieved over sulforesin KU-2.8.