Removal of sulfate from aqueous solution using Mg–Al nano-layered double hydroxides synthesized under different dual solvent systems

Author:

Liu Xiaobo1,Lu Shuang23,Tang Zhen23,Wang Zhaojia4,Huang Tianyong4

Affiliation:

1. Heilongjiang Province Hydraulic Research Institute , 78 Yanxing Road, Nangang District , Harbin 150080 , China

2. School of Civil Engineering, Harbin Institute of Technology , 150090 , Harbin , China

3. Key Lab of Structures Dynamic Behavior and Control of the Ministry of Education, Harbin Institute of Technology , Harbin 150090 , China

4. State Key Laboratory of Solid Waste Reuse for Building Materials, Beijing Building Materials Academy of Science Research , Beijing 100041 , China

Abstract

Abstract Because of its priority to remove anions, nano-layered double hydroxide (LDH) was incorporated to improve the sulfate attack corrosion resistance of cement-based materials. Herein, the synthesis of high-efficiency LDH for removal of SO 4 2 {\text{SO}}_{4}^{2-} is necessary. In this study, LDH with different Mg/Al ratios was synthesized under different dual solvent systems (water and ethylene glycol/ethanol/tetrapropylammonium hydroxide). Based on the adsorption experimental results, the LDH synthesized with n(Mg:Al) = 2:1 under water and ethanol solvent systems (ET2.0) exhibits the best adsorption capacity. The d (003) of LDH synthesized with n(Mg:Al) = 2:1 under different dual solvent systems are 0.7844, 0.7830, and 0.7946 nm, respectively. Three LDH belong to LDH- NO 3 {\text{NO}}_{3}^{-} . The results indicated that their surface charges show obvious difference synthesized under different dual solvent systems, which leads to differences in adsorption performance. The adsorption experimental results show that ET2.0 followed pseudo second-order kinetics and Langmuir model. The ET2.0 removed SO 4 2 {\text{SO}}_{4}^{2-} through anion substitution and electrostatic interaction and exhibited excellent adsorption rate with the maximum adsorption capacity of 95.639 mg/g. The effects of pore solution anion (OH, Cl, and CO 3 2 {\text{CO}}_{3}^{2-} ) on the removal of SO 4 2 {\text{SO}}_{4}^{2-} by the ET2.0 are limited.

Publisher

Walter de Gruyter GmbH

Subject

Surfaces, Coatings and Films,Process Chemistry and Technology,Energy Engineering and Power Technology,Biomaterials,Medicine (miscellaneous),Biotechnology

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