K. Laajalehto et al., XPS and FTIR study of the influence of electrode potential on activation of pyrite by copper or lead, COLL SURF A, 154(1-2), 1999, pp. 193-199
Citations number
16
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
Activation of pyrite by either copper or lead ions and subsequent xanthate
adsorption on activated surfaces were studied in aqueous solutions of pH 5,
6.5 and 9 under different electrochemical conditions using X-ray Photoelec
tron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR).
At pH 5, the copper concentration on the surface of pyrite increased stron
gly when the electrode potential was changed towards cathodic direction. At
low activation potentials (E-h less than or equal to + 100 mV), a change i
n the chemical state of sulfur on the surface was observed by XPS proposing
formation of a copper-containing surface sulfide phase. In electrochemical
ly-controlled xanthate adsorption, the behavior of copper-activated pyrite
resembled that of chalcopyrite (CuFeS2). The results indicate that activati
on of pyrite by copper at pH 5 can be controlled by the potential of the mi
neral. At pH 9. the copper content on the surface was independent of the po
tential of pyrite and no changes were observed in chemical state of sulfur
if compared to unactivated pyrite in the potential region - 100 to + 400 mV
(SHE). In the case of pyrite activation by lead, no changes were observed
in sulfur spectra at either pH 5 or 9 at different electrode potentials. Th
e concentration of lead on the surface increased at pH 5 when potential was
changed towards cathodic direction. All lead present at the surface of pyr
ite was concluded to be in the form of lead(II)-oxygen species and no evide
nce of exchange between lead and iron was found. Both adsorbed xanthate and
dixanthogen were observed on the surface of Cu-activated pyrite after acti
vation at cathodic potentials (- 100 to + 50 mV) and subsequent treatment i
n either ethyl or amyl xanthate solution of pH 5 or 6.5 at potential region
+ 350 to 550 mV (standard hydrogen electrode, SHE). In a similar experimen
ts with Pb-activated pyrite, only a faint indication of the adsorbed collec
tor species was found proposing that lead rather depresses than activates p
yrite. (C) 1999 Elsevier Science B.V. All rights reserved.