In situ electrochemical techniques and surface analysis were used to investigate the weathering behavior of arsenopyrite in chlorine-containing brine. Cyclic voltammetry measurements showed that arsenopyrite weathering releases S degrees, As (III) and Fe (II) during the initial step, even contains different concentrations of H+ and Cl-, and terminal transformation into SO42-, As (V) and Fe (III), respectively. Cl- ions promote the arsenopyrite weathering through diffusion control or adsorption control when Cl- ions are at low or high concentrations. When C-c1(-) increased from 0.00 to 0.05 mol/L, As (III) release increases from 549.33 to 1135.86 g.m(-2)y(-1), and the promotion efficiency is 107 %; whereas from 0.20 to 0.40 mol/L, the promotion efficiency is only 15.1 %. H+ ions accelerate arsenopyrite weathering for O-2 + 4H(+) + 4e(-)-> 2H(2)O, and the relationship between corrosion current density (i(corr)) and pH is i(corr) = - 26.54 pH + 199.75. Raman spectra confirm that corrosion produces S degrees and As (V) and EDX shows the passivation layers are mainly composed of elements Fe, As, S and O, while the adsorption layer are mainly composed of elements Fe, As, S and Cl. The experimental results are of great significance for arsenopyrite geological environment assess and removal of arsenic ions. 

 

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