Liquid chromatography of short chain carboxylic acids using a glutamic acid surfactant coated C18 stationary phase

Abd Al-Karim Fadhil Ali; Neil D Danielson

doi:10.1016/j.talanta.2020.120807

Liquid chromatography of short chain carboxylic acids using a glutamic acid surfactant coated C18 stationary phase

Talanta. 2020 Jun 1:213:120807. doi: 10.1016/j.talanta.2020.120807. Epub 2020 Feb 7.

Authors

Abd Al-Karim Fadhil Ali¹, Neil D Danielson²

Affiliations

¹ Department of Chemistry, 651 E. High Street, Miami University, Oxford, OH, 45056, USA.
² Department of Chemistry, 651 E. High Street, Miami University, Oxford, OH, 45056, USA. Electronic address: danielnd@miamioh.edu.

PMID: 32200935
DOI: 10.1016/j.talanta.2020.120807

Abstract

A C18 column was modified with the anionic amino acid surfactant lauroyl-l-glutamate (LLG) to facilitate the separation of ten short-chain aliphatic carboxylic acids (oxalic, tartaric, malic, malonic, lactic, acetic, maleic, citric, fumaric, and succinic). The developed method was proven to be fast, versatile, and environmentally friendly. After the coating of the column using 1% LLG solution and optimizing chromatographic conditions such as pH and temperature, near baseline resolution of the ten carboxylic acids within 4 min with excellent peak shape at pH = 1.8 using 100% H₂O acidified with sulfuric acid was possible. Although the design of this stationary phase, with the hydrophilic group at the end of the alkyl chain, seems to be in contrast to such columns designed for a totally aqueous mobile phase that have a polar (often amide) group embedded near the silica surface, no evidence of phase collapse was noted. Linear relationships of ln retention factor (k) versus 1/Temperature (T) (van't Hoff plots) were generated for all the acids indicating a single retention mechanism was likely. As the pH of the mobile phase decreased, the analyte retention factors increased due to the increase of the fraction of the analyte with neutral charge (alpha zero). The surfactant amide linkage, being electron donating, increased the pKa of the more acidic carboxyl group of glutamic acid so both carboxyl groups were protonated (neutral) at pH 1.8. The exact nature of the retention mechanism is uncertain but there certainly seems to be a pronounced hydrophobic component due to the large difference in retention of fumaric acid and methyl fumarate at pH 1.8. In addition, eleven beverage samples were analyzed for their aliphatic carboxylic acid contents. The results showed that malic, fumaric, and citric acids were the most common carboxylic acids in natural beverages with concentrations as high as 6432 ppm of malic acid in organic apple juice, 64 ppm of fumaric acid in organic concord juice, and 6543 ppm citric acid in strawberry lemonade juice.

Keywords: Aliphatic polar carboxylic acids; Amino acid surfactant; Green liquid chromatography.