4.7 Article

Enhanced adsorption of Congo red using chitin suspension after sonoenzymolysis

期刊

ULTRASONICS SONOCHEMISTRY
卷 70, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.ultsonch.2020.105327

关键词

Chitin suspension; Sonoenzymolysis; Congo red; Adsorption properties

资金

  1. National Key Research and Development Program of China [2016YFD0400301]
  2. Key Research and Development Program of Zhejiang Province [2017C02015]
  3. National Natural Science Foundation of China [31901822]

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Chitin suspensions treated with enzymolysis and sonoenzymolysis showed improved adsorption properties for Congo red dyes, with Langmuir isotherm and pseudo-second order model being more reliable in describing the adsorption process. Thermodynamic studies indicated a spontaneous adsorption process, with physical adsorption between chitin and CR confirmed through structural characterization before and after adsorption. Sonoenzymolysis resulted in a larger specific surface area and higher porosity, providing more active sites for adsorption.
In the present work, chitin suspensions after enzymolysis and sonoenzymolysis were taken as adsorbents to evaluate the adsorption properties of Congo red (CR) dyes. Compared with untreated chitin suspension, the CR adsorption performance was significantly improved after enzymolysis and even more after sonoenzymolysis. According to different adsorption kinetic and isotherm models, Langmuir isotherm and the pseudo-second order model were more reliable to describe the adsorption process of CR onto different chitin samples and demonstrated a monolayer and favorable physisorption process. What's more, negative values of Delta G (Gibbs free energy change) and the shifts to higher negative values with the temperature increasing from adsorption thermodynamic study proved a spontaneous CR adsorption process. The structural characterization before and after adsorption further verified the physical adsorption between chitin and CR, and a larger specific area and higher porosity of chitin suspension was obtained after sonoenzymolysis with more available active sites.

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