An examination of sodium alginate from Sargassum by NMR spectroscopy

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Abstract
Alginic acid, obtained from Sargassum brown algae that drift from the Sargasso Sea to beaches in Cuba, has been examined as an aqueous solution by 1H and 13C NMR spectroscopy, and also in the solid state by MAS 13C NMR spectroscopy. Its composition is distinctive, relative to that for alginic acid from most other brown algae, in having a lower content of β-D-mannopyranosyluronic acid residues (M) than of α-L-gulopyranosyluronic acid residues (G). That is, M/G is ~0.6, whereas ratios of >1 have been reported for many other species, including Macrocystispyrifera, which was examined here as well. In acquiring the high-resolution spectra, partial depolymerization was used to give solutions of reduced viscosity; as is well known, this procedure may cause separation into fractions and the formation of sediments, examples of which are cited. Proton resonances of the reducing end units of chain-shortened segments of the polymers exhibited unusual, marked, line broadening at elevated temperature, which may reflect thermal dehydration. MAS 13C experiments offered the advantage of information about the intact alginate samples. Although the spectra consisted of broad, heavily overlapping peaks, curve-fitting analysis afforded qualitative and quantitative data that supplement those obtained with solutions of the polymers. Keywords: Sargassum alginate, 1H NMR of fractions, M/G constituent ratios, MAS 13C NMR, curve-fitting analysis.

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