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

Author:

Yang Bingqiao123,Wu Jie45,Deng Bing1ORCID,Shao Hui3,Song Shaoxian5,Quintana Mildred6ORCID

Affiliation:

1. Technology Innovation Center for Comprehensive Utilization of Strategic Mineral Resources, Ministry of Natural Resources, Chengdu 610041, China

2. Hubei Three Gorges Laboratory, Yichang 443008, China

3. School of Resources and Safety Engineering, Wuhan Institute of Technology, Wuhan 430073, China

4. Doctorado Institucional de Ingeniería y Ciencia de Materiales, Universidad Autonoma de San Luis Potosi, Av. Sierra Leona 530, San Luis Potosi 78210, Mexico

5. School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan 430070, China

6. Facultad de Ciencias, Universidad Autonoma de San Luis Potosi, Av. Parque Chapultepec 1570, San Luis Potosi 78210, Mexico

Abstract

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.

Funder

National Natural Science Foundation of China

Hubei Science Foundation for Distinguished Young Scholars

Technology Innovation Center for Comprehensive Utilization of Strategic Mineral Resources, Ministry of Natural Resources

Consejo Nacional de Humanidades Ciencias y Tecnología (CONAHCYT) of Mexico

Publisher

MDPI AG

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