Study of Acid-Base Properties of Polymer Sorbents Based on Rhodanine Derivatives

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Abstract

The article presents the results of studies of acid-base properties of polymer sorbents based on rhodanine derivatives: polystyrene-azo-o-phenol-azorhodanine (PAFAR), ARA‑8p-p-carboxybenzene azorodane (ARA‑8p-p-KBAR) and AN‑31‑p-carboxybenzene azorodane (AN‑31‑p-KBAR). The sorption capacity of the sorbents for sodium ion and ionization constants of functional-analytical groups of sorbents were determined by potentiometric titration. The calculated values of sorption capacity for sodium ion for PAFAR, AN‑31‑p-KBAR and ARA‑8p-p-KBAR were 3,87 mmol/g, 13,27 mmol/g and 9,67 mmol/g, respectively. The values of the ionization constants of the functional groups of the sorbents were also calculated: for PAFAR – pK1 = 8,21 and pK2 = 9,39; AN‑31‑p-KBAR
– pK1 = 9,21 and pK2 = 10,16; ARA‑8p-p-KBAR – pK1 = 10,26 and pK2 = 10,80.

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About the authors

Saida M. Uvaisova

Dagestan Federal Research Center of the Russian Academy of Sciences (CIBR DFRC RAS)

Author for correspondence.
Email: smuvaisova@mail.ru
ORCID iD: 0000-0002-5100-2669

researcher at the Caspian Institute of Biological Resources

Russian Federation, Makhachkala

Magomed A. Babuev

DSU

Email: babuev77@mail.ru
ORCID iD: 0009-0009-2234-0982

PhD in Chemistry, Associate Professor of the Department of Analytical and Pharmaceutical Chemistry, Dean of the Faculty of Chemistry

Russian Federation, Makhachkala

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Central (1) non-differential (2) testable potentiometric curve (a), A-31-very-KBAR (b), surrounded by -8P-very-KBAR (C) (ms = 0.1 g, NaOH = 0.1 M, t = 20 ± 2 °C)

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3. Fig. 2. Graphical determination of the ionization constants of PHAGE PAPAR (a), AN-31-p-KBAR (b), ARA-8p-p-KBAR (c) (1 – pK1 and 2 – pK2)

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4. Table 1

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5. Table 2

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6. Table 3

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