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Development of an extraction procedure and analysis of electrostatically stabilized silanates from aqueous solutions Cover

Development of an extraction procedure and analysis of electrostatically stabilized silanates from aqueous solutions

Open Access
|Sep 2020

Abstract

The analyzed organosilicon derivatives of electrostatically stabilized silanates belong to a group of pentacoordinated compounds. These derivatives are: 1-(N-morpholiniomethyl)spirobi(1-sila-2,5-dioxacyclopentan-3-on)at, 1-(N-morpholiniomethyl)spirobi(1-sila-2,5-dioxa-4-methylcyclopentan-3-on)at, 1-(N-morpholiniomethyl) spirobi(1-sila-2,5-dioxa-4-(i-propyl)cyclopentan-3-on)at.

In the course of the work, the extraction process and optimization of conditions for separation and determination of a mixture of electrostatically stabilized silanates were carried out using capillary isotachophoresis. Proper leading electrolytes were elaborated developed and the terminating electrolyte: 4,4’-bis[(1-morpholiniomethyl)spirobi(1-sila-2,5-dioxacyclopentan-3-on)at] was proposed. The extraction process involved the use of three stationary phases: octadecyl, octyl and phenylpropyl. The highest recovery values, approx. 94%, were obtained on the phenylpropyl column. The optimum time of analysis by the isotachophoretic technique did not exceed 12 min. The developed method of separation and determination of electrostatically stabilized silanates expands the possibility of research on biological activity of this group of compounds in aqueous solutions and surface water vegetation.

DOI: https://doi.org/10.1515/ohs-2020-0022 | Journal eISSN: 1897-3191 | Journal ISSN: 1730-413X
Language: English
Page range: 247 - 254
Submitted on: Feb 21, 2020
Accepted on: Apr 9, 2020
Published on: Sep 25, 2020
Published by: University of Gdańsk
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2020 Joanna Jabłońska, Mariusz Kluska, Nikolai Erchak, Stanisław Popiel, published by University of Gdańsk
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.