The Deep Removal of Mercury in Contaminated Acid by Colloidal Agglomeration Materials M201

Author:

Qin Shuchen1,Yang Biwen1,Northwood Derek O.2,Waters Kristian E.3ORCID,Ma Hao1

Affiliation:

1. BGRIMM Technology Group, Beijing 100070, China

2. Department of Mechanical, Automotive and Materials Engineering, University of Windsor, 401 Sunset Avenue, Windsor, ON N9B 3P4, Canada

3. Department of Mining and Materials Engineering, McGill University, Montreal, QC H3A 2B1, Canada

Abstract

The high-temperature roasting/smelting process of copper and zinc concentrates will cause the mercury in the concentrate to evaporate into the flue gas, and most of the mercury in the flue gas will eventually enter the waste acid in its ionic form. A highly efficient mercury removal agent M201 with long carbon chains and loaded active functional groups can adsorb and disperse fine particles for mercury removal in the system. Through bridging, the linear structure is woven into a network to achieve large-scale capture and dispersion of fine particles and colloidal substances. The recommended operating conditions for developing mercury deep purification technology are as follows: M201 reagent concentration of 50 g/L, 6 mL/L added acid solution, room temperature, mixing time of 5 min, air flotation time of 10 min, ventilation rate of 0.1 L/min, H2SO4 concentration of 33.67 g/L, and the residual mercury content of 2 mg/L (the mercury content reaches 0.01 mg/L after two-stage mercury removal treatment). Meanwhile, the residual arsenic content is 21.9 mg/L. This study shows a better separation of arsenic and mercury and achieves one-step mercury removal.

Publisher

MDPI AG

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