中國有色金屬學(xué)報(英文版)
Transactions of Nonferrous Metals Society of China
| Vol. 32 No. 7 July 2022 |
（1. School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, China;
2. Department of Materials Science and Engineering, Southern University of Science and Technology, Shenzhen 518055, China）
Abstract:A continuous online in situ attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopic technique was used to investigate the adsorption and desorption kinetics of heptyl xanthate (KHX) on the surface of ZnO and Cu(II) activated ZnO. The results showed that Cu(II) facilitated the xanthate adsorption process on the surface, and led to the formation of cuprous xanthate (CuX), dixanthogen (X2) and xanthate aggregates. The adsorption of xanthate on the surface of ZnO and Cu(II) activated ZnO was found to both follow the pseudo-first-order kinetic model. When the NaOH solution was used as a desorption agent, the adsorbed xanthate can largely be removed due to the competition between OH- and HX-. However, for Cu(II) activated ZnO, the peak intensities at 1197 and 1082 cm-1 had no obvious weakening, and the absorption intensities at 1261 and 1026 cm-1 increased in the first 5 min, indicating an ion-exchange reaction between OH- and surface zinc bonded xanthate HX- and the reorganization of adsorbed xanthate.
Key words: ZnO; Cu(II) activation; continuous online in situ ATR-FTIR; heptyl xanthate; adsorption kinetics
