Pectin adsorption on amorphous Fe/Al hydroxides and its effect on surface charge properties and Cu(II) adsorption

Purpose

The purpose of this study was to elucidate the mechanisms for pectin-enhanced adsorption of heavy metal cations on variable charge minerals.

Materials and methods

Batch experiments were conducted to investigate the adsorption of pectin and copper(II) by amorphous Fe/Al hydroxides. The morphology, mineralogy, and functional groups of pectin–Fe/Al hydroxides were examined using X-ray diffraction, scanning electron microscopy, and Fourier transform infrared spectroscopy analysis.

Results and discussion

The amount of pectin adsorbed by amorphous Al(OH)₃ was much greater than that by amorphous Fe(OH)₃ at pH values between 3.5 and 6.5 due to the higher positive charge density on Al(OH)₃ and greater electrostatic attraction between the hydroxide and pectin compared with Fe(OH)₃. The addition of pectin decreased the positive surface charge on amorphous Fe and Al hydroxides. The presence of pectin enhanced the adsorption of Cu(II) by the Fe and Al hydroxides. The increase in Cu(II) adsorption on amorphous Fe hydroxide was more obvious at low pH values than at higher pH values, while an opposite changing trend was observed for amorphous Al hydroxide. At pH 3.9, 4.3, and 4.9, pectin increased Cu(II) adsorption by Fe hydroxide from 24.4, 76.6, and 177.0 mmol/kg to 61.6, 98.8, and 192.0 mmol/kg, i.e., Cu(II) adsorption was increased by 37.2, 22.2, and 15.0 mmol/kg, respectively. At pH 4.3 and 4.9, pectin increased Cu(II) adsorption by Al hydroxide from 3.7 and 27.0 mmol/kg to 17.3 and 69.4 mmol/kg, i.e., Cu(II) adsorption was increased by 13.6 and 42.4 mmol/kg, respectively. The greater adsorption of pectin by Al hydroxide was mainly responsible for the larger enhancement of pectin on Cu(II) adsorption on Al hydroxide at higher pH values compared with Fe hydroxide.

Conclusions

The adsorption of pectin on Fe and Al hydroxides decreased the positive charge on the hydroxides and thus enhanced the adsorption of Cu(II) by the hydroxides.