Chromium removal from aqueous solution by a PEI-silica nanocomposite.

Sci Rep

Center for Water Resource Cycle Research, Korea Institute of Science and Technology, Hwarang-ro 14-gil 5, Seongbuk-gu, Seoul, 02792, Republic of Korea.

Published: January 2018

AI Article Synopsis

  • Understanding the adsorption mechanism and removal efficiency is crucial for effectively using adsorption techniques to eliminate toxic heavy metals from wastewater.
  • The study focused on the chromium removal efficiency of a silica-based nanoparticle synthesized using a one-pot technique, which showed a high adsorption capacity of 183.7 mg/g.
  • Results indicated that the adsorption of chromium ions is influenced by solution pH and involves a reduction process, where Cr(VI) is transformed into Cr(III) and Cr, with different functional groups on the nanoparticle playing distinct roles in the adsorption.

Article Abstract

It is essential and important to determine the adsorption mechanism as well as removal efficiency when using an adsorption technique to remove toxic heavy metals from wastewater. In this research, the removal efficiency and mechanism of chromium removal by a silica-based nanoparticle were investigated. A PEI-silica nanoparticle was synthesized by a one-pot technique and exhibited uniformly well-dispersed PEI polymers in silica particles. The adsorption capacity of chromium ions was determined by a batch adsorption test, with the PEI-silica nanoparticle having a value of 183.7 mg/g and monolayer sorption. Adsorption of chromium ions was affected by the solution pH and altered the nanoparticle surface chemically. First principles calculations of the adsorption energies for the relevant adsorption configurations and XPS peaks of Cr and N showed that Cr(VI), [HCrO] is reduced to two species, Cr(III), CrOH and Cr, by an amine group and that Cr(III) and Cr(VI) ions are adsorbed on different functional groups, oxidized N and NH.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780388PMC
http://dx.doi.org/10.1038/s41598-018-20017-9DOI Listing

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