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Analytical Determination of Magnesium and Calcium in Diverse Matrices from Cyclopentane Hydrate Desalination. Cyclopentane Hydrate Desalination.

Ninh Hoai Duong 1
Dat Anh Nguyen 1
Quang Nhat Tran 1
Hai Son Truong-Lam 1, *
  1. Faculty of Chemistry, University of Science, Ho Chi Minh, 70000, Vietnam
Correspondence to: Hai Son Truong-Lam, Faculty of Chemistry, University of Science, Ho Chi Minh, 70000, Vietnam. Email: [email protected].
Volume & Issue: Vol. 29 No. 4 (2026) | Page No.: 4303-4311 | DOI: 10.32508/vnuhcmj-std.v29i4.4722
Published: 2026-10-17

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This article is published with open access by Viet Nam National University, Ho Chi Minh City, Viet Nam. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Abstract

Cyclopentane hydrate desalination has emerged as a promising low-energy alternative to con- ventional desalination because water forms hydrate lattices that encapsulate cyclopentane while excluding dissolved salts. In addition to producing fresh water, the proposed process analyzes streams such as seawater, hydrate-concentrated brine, and post-recovery process solutions that require accurate Ca2+ and Mg2+ determination for process monitoring, mass balance calculations, and resource recovery optimization. These ions are also precursors for high-value products such as struvite fertilizers, magnesium oxide nanoparticles, and hydroxyapatite materials. The process centers on an inexpensive ethylenediaminetetraacetic acid (EDTA) complexometric titration for Mg2+ and Ca2+ determination in diverse matrices associated with cyclopentane hy- drate desalination. It is compared for performance with flame atomic absorption spectroscopy (AAS). Total (Ca2+ + Mg2+) concentration was determined via titration with standardized EDTA at pH 10 using Eriochrome black T. Ca2+ concentration was determined at pH 12 using calcon after Mg2+ precipitation as magnesium hydroxide, and Mg2+ concentration was calculated as the dif- ference between the total and Ca2+ concentrations. Analytical conditions were optimized with respect to sample dilution factor, sodium chloride concentration, pH, indicator dosage, and poten- tial Sr2+ and boron species interferences. The proposed method demonstrated excellent linearity (R2 > 0.999), limits of detection (4.5 mg L−1 and 5.5 mg L−1 for Ca2+ and Mg2+, respectively,) recov- eries (98%–103%,) and relative standard deviations (below 3.5%). Statistical comparison with flame AAS showed excellent agreement without significant differences in precision or mean values based on F tests and Student's t tests at the 95% confidence level. The proposed method provides an ac- curate and economical analytical tool for Mg2+ and Ca2+ determination across multiple matrices and supports sustainable resource recovery.

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