4.7 Article

Effective removal of ammonium nitrogen using titanate adsorbent: Capacity evaluation focusing on cation exchange

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 771, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.144800

Keywords

Ammonium nitrogen; Cation exchange; Titanates; Ion selectivity; Affinity coefficient

Funding

  1. National Natural Science Foundation of China [51978569]
  2. Research Fund for Young Talent Support Plans of Xi'an Jiaotong University
  3. Shaanxi Key Research and Development Projects, China [2017SF-386]
  4. Fundamental Research Funds for the Central Universities of China

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This study focuses on the role of counter cations in the cation exchange process of NH4+ to enhance adsorption capacity. Different counter cations were found to affect the adsorption performance of titanates, with electrostatic interaction and ion affinity being the main influencing factors. The introduction of an affinity coefficient K-f helps explain the differences in adsorption performance among the titanates.
Cation exchange is one of the dominant mechanisms in the adsorption of cationic ammonium nitrogen (NH4+) from water. In this study, we focus on the role of counter cations in cation exchange process of NH4+ to enhance the adsorption capacity. Five amorphous titanates namely lithium titanate (LIT), sodium titanate (NaT), potassium titanate (KT), strontium titanate (SrT) and barium titanate (BaT) with different counter cation were facilely synthesized. The adsorption performance for NI-Li by these samples is in the order of LiT> NaT> KT> > SrT > BaT. The maximum adsorption capacity of LiT calculated by Langmuir is as high as 50.31 mg.g(-1). According to the experimental results and theoretical analysis, the electrostatic interaction between counter ions (cations in framework or eternal solution) and charged framework (fixed ions) is the main influence factor during cation exchange process in general. The cation valence and the hydrated ionic radius of the counter ions can inversely affect the ion exchange equilibrium and the affinity of counter ions to titanates. Therefore, a definition of a brief parameter, affinity coefficient K-f(relating to ion valence and distance between opposite charged ions), is introduced and used to explain the difference in adsorption performance of five titanates for NH4+. The conclusion about cation exchange and ions affinity may provide possible strategies for enhancement of cationic contaminant adsorption from water or wastewater. (C) 2021 Elsevier B.V. All rights reserved.

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