1. Adsorption behavior and selectivity mechanism of flotation reagents applied in ternary plastic mixtures.
- Author
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Zhao, Yue, Yang, Shengke, Wen, Hao, Shen, Zhou, and Han, Fengrong
- Subjects
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FLOTATION , *FLOTATION reagents , *ADSORPTION (Chemistry) , *ADSORPTION capacity , *POLYETHYLENE terephthalate , *MIXTURES - Abstract
• PET-PVC-PE mixtures can be separated via a two-stage flotation process. • First thermodynamic data for adsorption behavior of depressant SL. • Hydrogen bond based adsorption models of depressants are proposed for plastics. • Selectivity mechanism lies in supply of HBAs and HBDs. Plastic flotation attracts increasing attention in the process of recycling and will bring potential application in industry after theoretical perfection. For a separated ternary system of polyethylene terephthalate (PET), polyvinyl chloride (PVC) and polyethylene (PE), adsorption behavior and selectivity mechanism of flotation reagents were investigated by multi-characterization tests and batch equilibrium adsorption method. Quantitative adsorption results indicate that frother polyethylene glycol (PEG) only acts on gas and liquid phases in the flotation system with negligible adsorption capacity onto solid phase. For depressant sodium lignosulphonate (SL), the pseudo-first-order and Langmuir isotherm models are suitable for corresponding kinetic and equilibrium data of PET or PVC. Thermodynamic parameters further indicate that the adsorption of SL is a spontaneous and endothermic process, which neither belongs to the pure physisorption nor to the pure chemisorption. Adsorption models of SL were established based on hydrogen bond, with three clear bonding types (O H...π*, O H...O, and O H...Cl). Selectivity mechanism can be attributed to the selective hydrogen bond acceptors and donors, which are provided by specific plastic and depressant, respectively. In the light of these theoretical fundings, new targeted reagents or pre-treatments are expected to be developed towards more complex flotation system. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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