Analytical control of lactide synthesis; Petroleum and Coal; Vol. 58, iss. 5

Bibliographische Detailangaben
Parent link:Petroleum and Coal
Vol. 58, iss. 5.— 2016.— [P. 567-572]
Körperschaft: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра технологии органических веществ и полимерных материалов (ТОВПМ)
Weitere Verfasser: Krutas D. S. Darjya Sergeevna, Zamanova M. K. Margarita Karimovna, Lukjyanov A. E. Aleksandr Evgenjevich, Zinovyev (Zinovjev, Zinoviev) A. L. Alexey Leonidovich, Novikov V. T. Viktor Timofeevich, Volgina T. N. Tatiana Nikolaevna
Zusammenfassung:Title screen
The technique of identification and quantification of D,L-lactide, lactic acid and its oligomers by the method of high performance liquid chromatography (HPLC) was developed. The separation was done on two columns connected consecutively using an aqueous solution of orthophosphoric acid and acetonitrile in the ratio 88:12 vol. % at a flow rate of 1.2 ml min-1 as a mobile phase. The developed method is simple and linear. Research of specificity, accuracy, repeatability and reproducibility shows that the technique is suitable for analytical control of all stages of the lactide synthesis from lactic acid.
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Sprache:Englisch
Veröffentlicht: 2016
Schlagworte:
Online-Zugang:http://www.vurup.sk/wp-content/uploads/dlm_uploads/2017/07/pc_6_2016_krutas_volgina_488cor.pdf
Format: Elektronisch Buchkapitel
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=653525
Beschreibung
Zusammenfassung:Title screen
The technique of identification and quantification of D,L-lactide, lactic acid and its oligomers by the method of high performance liquid chromatography (HPLC) was developed. The separation was done on two columns connected consecutively using an aqueous solution of orthophosphoric acid and acetonitrile in the ratio 88:12 vol. % at a flow rate of 1.2 ml min-1 as a mobile phase. The developed method is simple and linear. Research of specificity, accuracy, repeatability and reproducibility shows that the technique is suitable for analytical control of all stages of the lactide synthesis from lactic acid.
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