Effects of sodium salt of N,N-dimethyldi-thiocarbamate on floatability of chalcopyrite, sphalerite, marmatite and its adsorption properties

Abstract

Effects of the sodium salt of N,N-dimethyldi-thiocarbamate (DMDC) in the absence and presence of butyl xanthate (BX) on the flotation of chalcopyrite, sphalerite, and marmatite have been investigated. Probable metal complexes and adsorption modes are inferred from UV–vis spectra, Fourier transform infrared (FTIR) and first-principles study. The results show that the presence of iron can reduce the activation of sphalerite, and marmatite can be depressed more readily than sphalerite. It has been found that in the presence of BX, a spot of DMDC can improve the recovery of chalcopyrite (pH 7.5), but is detrimental to the recovery of copper-activated sphalerite/mamatite; in addition, the copper-activated marmatite is depressed more obviously.The results of UV–vis spectra indicate that, DMDC has a stronger capacity of complex with Cu2+ than Zn2+, Fe2+. FTIR analysis shows that when the minerals are pre-treated by DMDC, BX can co-adsorb on the chalcopyrite surface, however, less BX species adsorb on sphalerite and marmatite surfaces. Analyses of group electro negativity calculation show that, compared with BX, the DMDC has stronger effects on the two minerals (chalcopyrite and sphalerite). The adsorption energy calculated also indicates a stronger interaction between DMDC and chalcopyrite (112) (−240.38kJ/mol) than that of sphalerite (110) (−81.65kJ/mol). The adsorption of DMDC on mineral surface occurs through the strong interaction of the S 3p orbital with the 3p, 3d orbital of Cu and 3d orbital of Zn atom. The electrons transfer from the Cu, Zn to S atom, respectively.