Adsorption of Glyphosate on Goethite:  Molecular Characterization of Surface Complexes

• Published in: Environmental science & technology Vol. 36; no. 14; pp. 3090 - 3095
• Main Authors: Sheals, Julia, Sjöberg, Staffan, Persson, Per
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 15.07.2002
• Subjects: Adsorption; Agronomy. Soil science and plant productions; analogs & derivatives; Applied sciences; Biological and medical sciences; Biological and physicochemical properties of pollutants. Interaction in the soil; Chemicals; Chemistry; Earth sciences; Earth, ocean, space; Engineering and environment geology. Geothermics; environmental fate; Exact sciences and technology; Fourier transforms; Fundamental and applied biological sciences. Psychology; Glycine; Glycine - analogs & derivatives; Glycine - chemistry; Glyphosate; Herbicides; Herbicides - chemistry; Hydrogen-Ion Concentration; Iron Compounds; Iron Compounds - chemistry; methods; Minerals; Molecules; Pollution; Pollution, environment geology; Scientific imaging; Soil and sediments pollution; Soil and water pollution; Soil science; Spectroscopy, Fourier Transform Infrared; Spectrum analysis; Water Purification; Water Purification - methods; Complexation; Surface reaction; Fourier transform spectroscopy; Molecular structure; Pollutant behavior; Pesticides; Crystal chemistry; Geochemistry; X ray; Soil pollution; Glyphosate; Herbicide; Iron Hydroxides oxides; Sorption; Infrared spectrometry; Adsorption; Aminoacid; Inner sphere; Reaction mechanism; Photoelectron spectrometry; Soil interaction; Goethite; Intramolecular hydrogen bond; Speciation
• ISSN: 0013-936X; 1520-5851; 1520-5851
• DOI: 10.1021/es010295w

As a component of herbicides, the fate of glyphosate (PMG) in the environment is of significant interest. The nature of PMG adsorption on mineral surfaces plays a significant role in the degradation of PMG. The adsorption of PMG on goethite (α-FeOOH) has been studied as a function of pH and PMG concentration. Adsorption was investigated with batch experiments, attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), and X-ray photoelectron spectroscopy (XPS). The N 1s line in XPS spectra showed deprotonation of the amine group of PMG (NH2 +) with increasing pH. IR analyses showed no evidence for the interaction of PMG's carboxylate group with the goethite surface, while the phosphonate group formed inner-sphere complexes. There is evidence for intramolecular hydrogen bonding between NH2 + and both the carboxylate and the phosphonate groups at low pH. Intramolecular hydrogen bonding is lost when the amine group is deprotonated, and the trend in intramolecular hydrogen bonding between NH2 + and phosphonate shows that PMG adsorbs via predominantly monodentate complexation. A minor quantity of bidentate complexes is thought to form both at near-neutral pH and when the surface concentration of PMG is low. While the phosphonate group of PMG binds directly, the carboxylate group remains relatively “free” from complexation with goethite, leaving it subject to degradation and/or complexation with metal ions present in the environment.