Issue 8, 2024, Issue in Progress

Graphene oxide functionalized with N-methyl-d-glucamine as a novel sorbent for boron removal from produced and formation waters

Abstract

This work describes the synthesis of a novel material based on graphene oxide (GO) for the selective removal of boron in an aqueous medium. The material was obtained by functionalizing graphene oxide with N-methyl-D-glucamine (NMDG). This material, named NMDG@GO, was successfully characterized using Fourier-transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction, thermogravimetric analysis, atomic force microscopy, and elemental analysis. The adsorption process was studied from a kinetic perspective using pseudo-first-order and pseudo-second-order models, with the pseudo-second-order model presenting a better fit. The adsorption process was studied using Langmuir and Freundlich isotherms, with the Freundlich model providing a better fit and an r2 value of 0.9368. This result indicates that the adsorption process occurred in multilayers, considering a heterogeneous distribution of adsorption sites. The levels of the factor's adsorbent mass, pH, and time were optimized using a central composite design, with the optimal values achieved at 120 mg of material, pH = 2.0, and an agitation time of 40 min. Under these optimized conditions, it was possible to remove 22 to 35% of the boron present in saline waters from oil production (production and formation waters) using the developed adsorbent.

Graphical abstract: Graphene oxide functionalized with N-methyl-d-glucamine as a novel sorbent for boron removal from produced and formation waters

Article information

Article type
Paper
Submitted
02 Jan 2024
Accepted
04 Feb 2024
First published
09 Feb 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 5319-5330

Graphene oxide functionalized with N-methyl-D-glucamine as a novel sorbent for boron removal from produced and formation waters

I. O. de Lucena, J. S. de Gois and R. J. Cassella, RSC Adv., 2024, 14, 5319 DOI: 10.1039/D4RA00037D

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