Adsorption of alpha amino acids at the water/goethite interface

• Published in: Journal of colloid and interface science 2008-03, Vol.319 (2), p.416-428
• Main Authors: Norén, Katarina, Loring, John S., Persson, Per
• Format: Article
• Language: English
• Subjects: Adsorption; Alanine - chemistry; Amino acids; Amino Acids - chemistry; ATR-FTIR spectroscopy; Chemistry; Colloidal state and disperse state; Edetic Acid - analogs & derivatives; Edetic Acid - chemistry; Exact sciences and technology; General and physical chemistry; Glycine - chemistry; Goethite; Iron Compounds - chemistry; Minerals; Models, Molecular; Sarcosine - chemistry; Spectrophotometry, Infrared; Spectroscopy, Fourier Transform Infrared; Spectrum Analysis; Surface physical chemistry; Water - chemistry; Water/mineral interface; X-Rays
• ISSN: 0021-9797; 1095-7103; 1095-7103
• DOI: 10.1016/j.jcis.2007.11.046

The adsorption of amino acids onto mineral surfaces plays an important role in a wide range of areas, e.g., low-temperature aqueous geochemistry, bone formation and protein–bone interactions. In this work, the adsorption of three alpha aminoacids (sarcosine, MIDA and EDDA) onto goethite ( α-FeOOH) was studied as a function of pH and background electrolyte concentration at 25.0 °C, and the molecular structures of the surface complexes formed were analyzed by means of ATR-FTIR spectroscopy. The results showed that adsorption of alpha amino acids were strongly dependent on the functionality and structure of the ligands. No adsorption was detected for the zwitterionic sarcosine indicating that simple alpha amino acids without other ionizable and/or functional groups display insignificant affinity for mineral surfaces such as goethite. With respect to the more complex amino acids, which are surface reactive, the number and relative positions of carboxylate and amine groups determine the types of surface interactions. These interactions range from non-specific outer-sphere to specific inner-sphere interactions as shown by the MIDA and EDDA results, respectively. The results presented herein suggest that isomerically-selective adsorption might only occur for amino acids that are capable of specific surface interactions, either through site-specific hydrogen bonding or inner-sphere complexation. The ATR-FTIR spectra and the 2D contour plot reveal two EDDA surface complexes at the water/goethite interface.