TY - JOUR
T1 - Electrolysis Oxidation of Chalcopyrite and Molybdenite for Selective Flotation
AU - Miki, Hajime
AU - Matsuoka, Hidekazu
AU - Hirajima, Tsuyoshi
AU - Suyantara, Gde Pandhe Wisnu
AU - Sasaki, Keiko
PY - 2017
Y1 - 2017
N2 - Electrolysis oxidation of chalcopyrite and molybdenite was investigated, via various electrochemical methods, with the aim of realizing selective flotation of these minerals. Result of potential polarization indicated that oxidation via electrolysis affected only the chalcopyrite surface, owing mainly to the difference in conductivity of these minerals. Also measurements of contact angle after electrolysis indicated that contact angle of chalcopyrite selectively decreased whereas that of molybdenite did not decrease drastically. XPS analyses after electrolysis indicated that chalcopyrite peak decreased whereas iron oxyhydroxide (goethite) and iron sulfate increased, it suggests that these oxidation products covered on the surface of chalcopyrite. On the other hand, molybdenite peak is similar after electrolysis except for molybdenum oxide/oxygen with molybdenite can be seen for oxygen peak. From these results and general knowledge that sulfide hydrophobicity and sulfate/oxyhydroxide hydrophilicity, it can be explained that with electrolysis oxidation, hydrophilic oxihydroxide and sulfate covered on the surface of hydrophobic chalcopyrite then chalcopyrite surface became hydrophilic. On the other hand, molybdenite surface keep hydrophobic since its difficulty of oxidation and it is difficult to stay molybdenum oxide on the surface due to its soluble property. These results revealed that chalcopyrite was selectively oxidized and, hence, selective flotation of chalcopyrite and molybdenite was possible. This electrolysis oxidation methods were compared with those governing other oxidation treatments.
AB - Electrolysis oxidation of chalcopyrite and molybdenite was investigated, via various electrochemical methods, with the aim of realizing selective flotation of these minerals. Result of potential polarization indicated that oxidation via electrolysis affected only the chalcopyrite surface, owing mainly to the difference in conductivity of these minerals. Also measurements of contact angle after electrolysis indicated that contact angle of chalcopyrite selectively decreased whereas that of molybdenite did not decrease drastically. XPS analyses after electrolysis indicated that chalcopyrite peak decreased whereas iron oxyhydroxide (goethite) and iron sulfate increased, it suggests that these oxidation products covered on the surface of chalcopyrite. On the other hand, molybdenite peak is similar after electrolysis except for molybdenum oxide/oxygen with molybdenite can be seen for oxygen peak. From these results and general knowledge that sulfide hydrophobicity and sulfate/oxyhydroxide hydrophilicity, it can be explained that with electrolysis oxidation, hydrophilic oxihydroxide and sulfate covered on the surface of hydrophobic chalcopyrite then chalcopyrite surface became hydrophilic. On the other hand, molybdenite surface keep hydrophobic since its difficulty of oxidation and it is difficult to stay molybdenum oxide on the surface due to its soluble property. These results revealed that chalcopyrite was selectively oxidized and, hence, selective flotation of chalcopyrite and molybdenite was possible. This electrolysis oxidation methods were compared with those governing other oxidation treatments.
U2 - 10.2320/matertrans.M-M2017807
DO - 10.2320/matertrans.M-M2017807
M3 - Article
SN - 0916-1821
VL - 58
SP - 761
EP - 767
JO - Materials Transactions
JF - Materials Transactions
IS - 5
ER -