Improving the Flotation of Unoxidized and Oxidized Molybdenite Fines Using Dodecylamine as a Collector: Flotation Tests and Interaction Mechanism

The flotation of unoxidized and oxidized molybdenite fines is a challenging job worldwide. In this work, dodecylamine (DDA) was developed as a potential collector to improve the flotation of molybdenite fines with and without oxidation. The flotation behaviors and interaction mechanisms were probed...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Minerals (Basel) 2024-05, Vol.14 (5), p.468
Hauptverfasser: Yang, Bingqiao, Wu, Jie, Deng, Bing, Shao, Hui, Song, Shaoxian, Quintana, Mildred
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The flotation of unoxidized and oxidized molybdenite fines is a challenging job worldwide. In this work, dodecylamine (DDA) was developed as a potential collector to improve the flotation of molybdenite fines with and without oxidation. The flotation behaviors and interaction mechanisms were probed through flotation tests, contact angle, Zeta potential, Scanning Electron Microscope-Energy Dispersive Spectrometer(SEM-EDS), and X-ray Photoelectron Spectroscopy (XPS). The flotation tests revealed that DDA improved the flotation of unoxidized or oxidized molybdenite fines efficiently. The results of Zeta potential, contact angle, and SEM-EDS uncovered that a substantial number of DDA species adsorbed on both fresh and oxidized molybdenite faces and edges, thus enhancing their hydrophobicity. XPS analysis further manifested that RNH2 and RNH3+ adsorbed on the S atoms of fresh faces through hydrogen bonding. Meanwhile, RNH2 and RNH3+ mainly adsorbed on fresh edges via chemical bonding between amine groups and Mo sites and electrostatic force. For oxidized molybdenite, RNH2 and RNH3+ interacted with oxidized faces through hydrogen bonding while adsorbed on oxidized edges via hydrogen bonding and electrostatic interaction.
ISSN:2075-163X
2075-163X
DOI:10.3390/min14050468