A multi-technique study of the effect of aqueous aluminium speciation on hydrolytic gelation of aluminium (oxy)hydroxide.

J Colloid Interface Sci

School Science and Technology, Nottingham Trent University, Clifton Lane, Nottingham NG11 8NS, UK.

Published: April 2009

AI Article Synopsis

  • The study focuses on how aluminium ions in water transform into aluminium (oxy)hydroxides when a Tris-buffer is added, utilizing techniques like pH, conductivity, viscosity, and ultrasound measurements.
  • The research identifies key phases in the sol-gel transformation, including the change from aluminium clusters to nanoparticles, aggregation of these particles, and the formation of a gel network.
  • It highlights the role of aluminium ion speciation in the transformation process and demonstrates that ultrasound is an effective method for observing later stages of aluminium (oxy)hydroxide formation and breakdown.

Article Abstract

The sol-gel transformation of aqueous solutions of aluminium ions into aluminium (oxy)hydroxides induced by the addition of a 'soft base'-'Tris-buffer' (pK(a)=8.2) has been investigated using monotonous single-batch titrations and a combination of four complimentary techniques for monitoring pH, conductivity, viscosity and ultrasound parameters (velocity and attenuation). The multi-probe monitoring of the formation of aluminium (oxy)hydroxides enabled important stages of the sol-gel transformation process including: the structural conversion of aluminium Keggin-like polynuclear clusters into nanoparticles of aluminium (oxy)hydroxide; the aggregation of primary nuclei of aluminium (oxy)hydroxide into larger particles, and the 'arrested growth' of the aggregates with the formation of the three-dimensional gel network to be followed. The effect of aluminium ion molecular speciation on the sol-gel transformation stages is discussed. The data presented show that ultrasonic spectrometry, although a novel tool for sol-gel studies, is beneficial for the non-invasive monitoring of the latter stages of aluminium (oxy)hydroxide formation and its eventual breakdown in the presence of excess base.

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http://dx.doi.org/10.1016/j.jcis.2008.12.042DOI Listing

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