Adsorption of phenylalanine on layered double hydroxides: effect of temperature and ionic strength

In this work we report the adsorption of phenylalanine (Phe) on Magnesium Aluminum Layered Double Hydroxides (Mg–Al–CO₃-LDH) at two different temperatures (298 and 310 K) and under two distinct ionic strength conditions (with and without the addition 0.1 M of NaCl). The adsorption isotherms exhibit...

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Bibliographic Details
Published inJournal of materials science Vol. 43; no. 2; pp. 434 - 439
Main Authors Silvério, Fabiano, dos Reis, Márcio José, Tronto, Jairo, Valim, João Barros
Format Journal Article Conference Proceeding
LanguageEnglish
Published Boston Springer US 2008
Springer
Springer Nature B.V
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Summary:In this work we report the adsorption of phenylalanine (Phe) on Magnesium Aluminum Layered Double Hydroxides (Mg–Al–CO₃-LDH) at two different temperatures (298 and 310 K) and under two distinct ionic strength conditions (with and without the addition 0.1 M of NaCl). The adsorption isotherms exhibit the same profile in all conditions, and they only differ in the amount of removed Phe. At lower ionic strength, the isotherms are almost identical at both temperatures, except for the last points, where the increase in temperature causes a decrease in the amount of adsorbed Phe. An increase in ionic strength results in a decrease in Phe adsorption. The electrokinetic potential decreases as the amount of adsorbed Phe increases, and only positive values are observed. This indicates that the surface of the adsorbent is not totally neutralized and suggests that more Phe could be removed by adsorption. The presence of Phe on the solid is confirmed by FTIR spectra, which present the specific bands assigned to Phe. The hydrophobicity of the amino acid probably contributes to its extraction, thus enabling the removal of a great amount of Phe. In conclusion, LDH is potentially applicable in the removal of Phe from wastewater.
Bibliography:http://dx.doi.org/10.1007/s10853-007-2202-9
ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0022-2461
1573-4803
DOI:10.1007/s10853-007-2202-9