4.7 Article

Influence of aromatic structure and substitution of carboxyl groups o aromatic acids on their sorption to biochars

Journal

CHEMOSPHERE
Volume 210, Issue -, Pages 239-246

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2018.07.003

Keywords

Biochar; Sorption; Aromatic structure; -COOH substitution; Dissociation

Funding

  1. National Natural Science Foundation of China [51238001]
  2. Beijing Natural Science Foundation [8162021]
  3. Fundamental Research Funds for the Central Universities [2652017181]

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In order to clarify the influence of aromatic structure and -COOH substitution of aromatic acids on their sorption to biochars, benzoic acid (BA), phthalic acid (PA), hemimellitic acid (HA), 2-biphenylcarboxylic acid (2-BA), 1-naphthoic acid (1-NA) and naphthalene were selected as model sorbates. Batch experiments on sorption of them to wheat straw-derived biochars at 300 degrees C (WS300) and 700 degrees C (WS700) were conducted. Results showed that WS700 with higher specific surface area and pore volume had faster and higher sorption of aromatic acids than WS300. Sorption affinity of aromatic acids decreased with increasing number of aromatic rings (BA> 1-NA > 2-BA), and was weakened by -COOH substitution (BA> PA > HA). This was likely due to the is-electron delocalization into additional ring, reduced contact area of nonplanar aromatic structure on biochar surfaces, size exclusion of larger molecules in smaller pores of biochars and decreased hydrophobicity of aromatic acids by -COOH substitution that abated the sorption. Dissociation of -COOH substitution of aromatic acids also weakened their sorption to biochars due to the lower hydrophobicity of anionic species, and electrostatic repulsion between anionic species and negatively charged surface of biochars. (C) 2018 Elsevier Ltd. All rights reserved.

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