Low Temperature n-alkanes Bromination without Catalysts

Bibliographic Details
Parent link:Procedia Chemistry
Vol. 11 : 1st International Symposium on Inorganic Fluorides: Chemistry and Technology, ISIF 2014, Tomsk, Russia.— 2014.— [P. 84-87]
Corporate Authors: Национальный исследовательский Томский политехнический университет (ТПУ) Физико-технический институт (ФТИ) Кафедра химической технологии редких, рассеянных и радиоактивных элементов (№ 43) (ХТРЭ), Национальный исследовательский Томский политехнический университет (ТПУ) Институт физики высоких технологий (ИФВТ) Кафедра биотехнологии и органической химии (БИОХ)
Other Authors: Sobolev V. I. Vasily Igorevich, Radchenko V. B. Vyacheslav Borisovich, Ostvald R. V. Roman Vyacheslavovich, Filimonov V. D. Viktor Dmitrievich, Zherin (Gerin) I. I. Ivan Ignatyevich
Summary:Title screen
It has been observed that Ba (BrF[4])[2] demonstrated a high reactivity towards normal alkanes from C[6]H[14] to C[16]H[34]. It has been found that the reactions ran with intensive self-heating and release of elemental bromine. The GC-MS analysis showed that the main product of Ba (BrF[4])2 interaction with each alkane was its 3-bromoderivative. The optimal interaction parameters have been found. The heat effects of the reaction have been determined by the isothermal calorimetric method, it has been found that the heat effect of the bromination increased with the increase of the length of carbon chain of alkane.
Режим доступа: по договору с организацией-держателем ресурса
Language:English
Published: 2014
Subjects:
Online Access:http://dx.doi.org/10.1016/j.proche.2014.11.015
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=639603