4.7 Article

New insights into the fate and interaction mechanisms of hydrolyzed aluminum-titanium species in the removal of aged polystyrene

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 464, Issue -, Pages -

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ELSEVIER
DOI: 10.1016/j.jhazmat.2023.133010

Keywords

PS microplastics; Composite coagulant; 2D-FTIR-COS; Dominant species; Interaction process

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The interaction process between polyaluminum-titanium chloride composite coagulant (PATC) and aged polystyrene powder (APSp) was studied. The rise of O-containing functional groups in APSp increased the formation of C-O-M coordination bonds and hydrogen bonds, improving the removal of PSp. Al13(OH)53Ti13O17(H2O)20 electrostatic attraction brought Al13Ti13 close to APSp, followed by hydrogen bonding and complexation. However, the Al13Ti13-APSp complexes were easily converted to monomers and dimers during coagulation, affecting the coagulation efficiency.
Polyaluminum-titanium chloride composite coagulant (PATC) has been demonstrated to be a promising coagulant in microplastics (MPs) treatment. However, the interaction process between the dominant species of PATC and MPs remains unclear, which will hinder our understanding of the coagulation mechanisms. Here, the species transformation of PATC during its interaction with aged polystyrene powder (APSp) was studied. The results showed that the rise of O-containing functional groups in APSp increased the possibility of forming C-O-M coordination bonds and hydrogen bonds between APSp and PATC, which improved the removal of PSp. Furthermore, Al13(OH)53Ti13O17(H2O)20 electrostatic attraction brought Al13Ti13 approached APSp first, followed by hydrogen bonding and complexation occurred, respectively. However, the Al13Ti13-APSp complexes were easily converted to monomers and dimers during coagulation, which influenced the coagulation efficiency. With the increase of pH, OH- in the solution would further polymerize the depolymerized Al2Ti into oligomers and mesomers. Under weakly acid conditions, the diversity of PATC hydrolysates and the increase in APSp binding sites correspondingly led to the maximum APSp removal of 75%. When the pH further increased to 10, PATC interacted with APSp mainly by hydrogen bonding and sweeping effect.

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