Collecting property of diphosphonic acid for niobite

来源 :Journal of University of Science and Technology Beijing(Engl | 被引量 : 0次 | 上传用户:icenum123
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The effect of several collectors on the niobite synthetized under the condition of varying pH values and dosages were studied. The collecting property of several representative collectors was also investigated. The experimental result shows that di- phosphonic acid is a good collector for niobite. Its recovery is about 84.24%-91.17% when the pH value of the pulp is less than 5.0 and the dosage of diphosphonic acid is 140 mg/L. The sequences of the selectivity and collecting capacity of the collectors were compared. Infrared absorption spectrum (IAS) and X-ray photoelectron spectroscopy (XPS) were used to detect and analyze the ad- sorption mechanism of diphosphonic acid on the surface of niobite. The IAS result indicates that diphosphonic acid is indeed ad- sorbed on the surface of niobite, and the XPS result shows that the binding energy of P2p peak of niobite treated by diphosphonic acid has changed 2.85 eV. It confirms that the adsorption belongs to a chemisorption type. The effect of several collectors on the niobite synthetized under the condition of varying pH values ​​and dosages were studied. The collection property of several representative collectors was also investigated. The experimental result shows that di- phosphonic acid is a good collector for niobite. Its recovery is about 84.24% -91.17% when the pH value of the pulp is less than 5.0 and the dosage of diphosphonic acid is 140 mg / L. The sequences of the selectivity and collecting capacity of the collectors were compared. Infrared absorption spectrum (IAS) and X-ray photoelectron spectroscopy (XPS) were used to detect and analyze the ad-sorption mechanism of diphosphonic acid on the surface of niobite. The IAS result that the diphosphonic acid is indeed ad- sorbed on the surface of niobite, and the XPS result shows that the binding energy of P2p peak of niobite treated by diphosphonic acid has changed 2.85 eV. It confirms that the adsorption belongs to a chemisorption type.
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