Comparative evaluation of different collector–depressant systems application in the reverse flotation of apatite and collophane from a sedimentary phosphate ore sample

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Authors: Esmaeel Talebi, Hassan Maleki, Sepideh Langari, Mohammad Noaparast, Sied Ziaedin Shafaei, Golnaz Jozanikohan
Cited by: 4
References: 25

Abstract

This study presents a comparative evaluation of various collector-depressant systems application in the reverse flotation of apatite and collophane from a low-grade sedimentary phosphate ore sourced from the Koh-e-Lar phosphate deposit. The ore, characterized by high carbonate (calcite) and silicate (quartz) impurities, underwent de-sliming via hydrocyclone to remove particles finer than 38 µm, reducing slime interference and resulting in approximately 12.2% P 2 O 5 loss in a single stage. Reverse flotation experiments were conducted to depress phosphate minerals while floating gangue, focusing on the effects of pH, collector types (oleic acid, Pamak 200, Armac T, OMC A 308, Pamak 4), depressant systems (aluminum sulfate-potassium sodium tartrate combinations), and collector mixtures. Optimal conditions were identified at natural pH (5–7), where oleic acid and Pamak 200 exhibited superior selectivity with enrichment ratios around 1.4. The 2:1 ratio of aluminum sulfate to potassium sodium tartrate provided the best depression, enhancing carbonate flotation. Collector mixtures of oleic acid: Pamak 200 at 30:70 and 50:50 ratios yielded the highest P 2 O 5 grades (up to 13%) and recoveries (rougher up to 90.1%, final up to 56.8% including slimes). These findings suggest potential complementary interactions between mixed reagents that improved selectivity and flotation efficiency, although further surface characterization would be required to confirm the underlying mechanisms.

Fields of Study & Subjects

Minerals Flotation and Separation Techniques Metal Extraction and Bioleaching Extraction and Separation Processes

Publication details

Journal / source
Results in Engineering
Publisher
Elsevier BV
Volume
30
Pages
110544–110544
Publication date
16 April 2026
Language
EN