A high-efficiency hydrocyclone designed by response surface methodology for acid hydrolysis residue recycling

Author:

Xu Yanxia1ORCID,Tang Bo1,Song Xingfu1,Yu Jianguo1

Affiliation:

1. National Engineering Research Centre for Integrated Utilization of Salt Lake Resource, School of Resources and Environmental Engineering, East China University of Science and Technology, Shanghai 200237, People's Republic of China

Abstract

A high-efficiency hydrocyclone was designed by response surface methodology to evaluate the recycling of acid hydrolysis residues from titanium dioxide (TiO 2 ) production as a study case. TiO 2 is an important product and the world's best white pigment. During its production from ilmenite (FeTiO 3 ) by the sulfuric acid method, the incomplete reaction produces large amounts of residue, which also contain unreacted ilmenite. Large amounts of residue are generally accumulated without any treatment. Hydrocyclone use is regarded as a method for separating and recovering chemicals from process residues by which the unreacted components can be recycled efficiently. However, hydrocyclones designed by conventional procedures may have some limitations regarding classification sharpness. In this paper, numerical experiments and laboratory tests were performed to evaluate the classification sharpness of various hydrocyclone designs. Response surface methodology was used to optimize hydrocyclones with different structural configurations. Based on the response models, a designed hydrocyclone with a high sharpness of classification of particles was constructed. The sharpness of the newly designed hydrocyclone increased from 80.5% to 93.3%. The vortex finder separated approximately 89.9% of the fine particles in impurities, while 51.0% of TiO 2 was recycled by the spigot. The hydrocyclone proposed in this paper properly minimizes the risk of environmental pollution caused by TiO 2 production and provides a significant estimated cost savings.

Funder

National Natural Science Foundation of China

Publisher

The Royal Society

Subject

Multidisciplinary

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