Equilibrium and Kinetic Modeling of Crystal Violet Dye Adsorption by a Marine Diatom, Skeletonema costatum

Abstract

Significant efforts have been made to improve adsorbents capable of eliminating pollutants from aqueous solutions, making it simple and quick to separate from the treated solution. In the current study, the removal of Crystal Violet Dye (CVD) from an aqueous synthetic solution onto a marine diatom alga, Skeletonema costatum, was investigated. Different experiments were conducted as a function of different pH, contact time, adsorbent dosage, temperature, and initial CVD concentration. The highest adsorption efficiency (98%) was obtained at 0.4 g of S. costatum, pH 3, and a contact time of 120 min, at 25 °C. Furthermore, Fourier-transform infrared spectroscopy (FTIR) results display that binding of CVD on S. costatum may occur by electrostatic and complexation reactions. Moreover, the Brunauer–Emmett–Teller surface area analysis (BET) obtained was 87.17 m2 g−1, which, in addition to a scanning electron microscope (SEM), reveals large pores that could enhance the uptake of large molecules. However, the equilibrium adsorption models were conducted by Halsey, Langmuir, Freundlich, Henderson, and Tempkin isotherm. In addition, multilayer adsorption isotherm best described the uptake of CVD onto S. costatum. The maximum monolayer adsorption capacity (qmax) was 6.410 mg g−1. Moreover, thermodynamic parameters of the adsorption studies suggested that the uptake of CVD onto S. costatum was endothermic and spontaneous. The pseudo-first-order, pseudo-second-order, and intra-particle diffusion kinetic equations were applied to model the adsorption kinetic data. It was seen that the kinetics of the adsorption may be described using pseudo-second-order kinetic equations. Finally, the present work concluded that the marine diatom alga S. costatum is suitable as a natural material for the adsorption of CVD.