High efficiency of treated-phengite clay by sodium hydroxide for the Congo red dye adsorption: Optimization, cost estimation, and mechanism study.

Wastewater textile dye treatment is a challenge that requires the development of eco-friendly technology to avoid the alarming problems associated with water scarcity and health-environment. This study investigated the potential of phengite clay as naturally low-cost abundant clay from Tamgroute, Morocco (TMG) that was activated with a 0.1 M NaOH base (TMGB) after calcination at 850 °C for 3 h (TMGC) before its application in the Congo red (CR) anionic dye from the aqueous solution. The effect of various key operational parameters: adsorbent dose, contact time, dye concentration, pH, temperature, and the effect of salts, was studied by a series of adsorption experiments in a batch system, which affected the adsorption performance of TMG, TMGC, and TMGB for CR dye removal. In addition, the properties of adsorption kinetics, isotherms, and thermodynamics were also studied. Experimental results showed that optimal adsorption occurred at an acidic pH. At a CR concentration of 100 mg L-1, equilibrium elimination rates were 68%, 38%, and 92% for TMG, TMGC, and TMGB, respectively. The adsorption process is rapid, follows pseudo-second-order kinetics, and is best described by a Temkin and Langmuir isotherm. The thermodynamic parameters indicated that the adsorption of CR onto TMGB is endothermic and spontaneous. The experimental values of CR adsorption on TMGB are consistent with the predictions of the response surface methodology. These led to a maximum removal rate of 99.97% under the following conditions: pH = 2, TMGB dose of 7 g L-1, and CR concentration of 50 mg L-1. The adsorbent TMGB's relatively low preparation cost of around $2.629 g-1 and its ability to regenerate in more than 6 thermal calcination cycles with a CR removal rate of around 56.98%, stimulate its use for textile effluent treatment on a pilot industrial scale.

Novel insights into crystal violet dye adsorption onto various macroalgae: Comparative study, recyclability and overview of chromium (VI) removal.

In this study, effective biomaterials were prepared from marine macroalgae, namely Fucus spiralis (F.S), Ulva intestinalis (U.I), and Corallina officinalis (C.O). The ability to adsorb the hazardous organic dye crystal violet (CV) was examined, revealing different adsorptive properties for the three algae. The removal of CV dye occurred onto only a homogeneous monolayer for F.S, and both a homogeneous monolayer and a heterogeneous multilayer for U.I and C.O algae. The predicted monolayer capacities at 25 °C were approximately 53 mg/g, 55 mg/g, and 97 mg/g for F.S, C.O, and U.I, respectively. The adsorption of CV dye on all the algae was found to follow a pseudo-second-order rate. Ulva intestinalis algae, as a potential adsorbent of CV dye, were also tested in the adsorption of inorganic substances and demonstrated significant efficiency in the removal of chromium (VI). The findings highlight various adsorption properties and the relevance of macroalgae for wastewater treatment applications.

Application of Taguchi method, response surface methodology, DFT calculation and molecular dynamics simulation into the removal of orange G and crystal violet by treated biomass.

In this work, the efficiency of the treated plant Carpobrotus edulis (TPCE) as an effective biosorbent for removing the orange G (OG) and crystal violet (CV) dyes from aqueous solution was investigated. TPCE was characterized by FT-IR, Ss, pHz and SEM-EDX. The influence of parameters such as bioadsorbent dose, contact time, initial concentration, temperature and pH was tested using Taguchi experimental design (TED) with L8 orthogonal array (five parameters in two levels). The initial concentration, bioadsorbent dose and contact time are the main parameters for the removal of CV and OG dyes, while the effects of pH and temperature are minimal. The maximum removal efficiency of dyes under optimal operating conditions was 97.93 % and 92.68 %, respectively. which at the optimal conditions of 3 g/L, pH 10, 20 mg/L, 35 °C, 5 min and 15 g/L, pH 4, 20 mg/L, 35 °C, 60 min for CV and OG dyes, respectively. The results of response surface methodology (RSM) and analysis of variance (ANOVA) showed that the initial concentration Ci of CV dye was the most significant factor in the adsorption efficiency with a contribution of 51.56 %. On the other hand, the OG bioadsorbent dose is the most important factor in adsorption efficiency with a percentage contribution of 56.41 %. The Density Functional Tight Binding (DFTB) method shows that dyes strongly bind the adsorbent surface. Monte Carlo and molecular dynamics simulations show significant interactions between dye and adsorbent surface. The reusability of biomaterial indicated that the adsorption performance dropped very slightly up to five cycles.

Efficient removal of Cr (VI) from aqueous solution using memory effect property of layered double hydroxide material.

Treating wastewater containing pollutants with layered double hydroxide (LDH) material attracts excellent interest. LDH materials are known by the memory effect property, which leads to the reconstruction of the LDH structure after its calcination and rehydration. In this study, LDH material was prepared, calcined, and then rehydrated in an aqueous Cr(VI) solution. XRD, FTIR, and SEM-EDS analysis confirm the successful reconstruction of LDH-loading chromium on its surface and layered space. Response surface methodology (RSM) results showed that LDH mass, contact time, and chromium concentration are the main factors controlling the removal of Cr(VI). The heterogeneous sorption of chromium was described by fitting the equilibrium data to the Freundlich model. Analytical techniques, thermodynamic data, activation, and adsorption energies confirm that the removal process of Cr(VI) is endothermic, spontaneous, and physical nature. LDH exhibits good reusability performance with only a 7% reduction of initial adsorption capacity after five cycles of the calcination-rehydration process. These results show that the memory effect of LDH is helpful for the intercalation and the removal of emergent pollutants, especially for wastewater treatment.

An efficient and adsorption of methylene blue dye on a natural clay surface: modeling and equilibrium studies.

The present research work revolves around the evaluation of the elimination of the cationic dye methylene blue (MB) from an aqueous solution by the exploitation of natural clay (TMG) from South-East Morocco. Several physicochemical techniques were used to characterize our TMG adsorbate, namely, X-ray diffraction, Fourier transform infrared absorption spectroscopy, differential thermal analysis, thermal gravimetric analysis, and zero charge point (pHpzc). The morphological properties and elemental composition of our material were identified using scanning electron microscopy coupled with an energy-dispersive X-ray spectrometer. The batch technique was used under different operating conditions to produce quantitative adsorption, namely, the amount of adsorbent, dye concentration, contact time, pH, and solution temperature. The maximum adsorption capacity of MB on TMG was 81.185 mg g-1 for a concentration of 100 mg L-1 MB at pHinitial = 6.43 (no initial adjustment of the pH-value was performed), temperature 293 K, and 1 g L-1 adsorbent. The adsorption data were examined by Langmuir, Freundlich, and Temkin isotherms. The Langmuir isotherm provides the best correlation with the experimental data, and the pseudo-second-order kinetic model is more appropriate for the adsorption of the MB dye. The thermodynamic study of MB adsorption indicates that the process is physical, endothermic, and spontaneous. The Box-Behnken method was applied to identify the optimal conditions for MB removal in the design of batch experiments. The parameters examined result in >99% removal. The TMG material's regeneration cycles and low cost ($0.393 per gram) show that it is both environmentally friendly and very effective for dye removal in the various textile sectors.

Synthesis, characterization, and comparative study of MgAl-LDHs prepared by standard coprecipitation and urea hydrolysis methods for phosphate removal.

Layered double hydroxides (LDHs), known as a class of anionic clays, have attracted considerable attention recently due to their potential applications in different areas as catalyst materials, energy materials, and adsorbent materials for environmental remediation, especially for anionic pollutant removal. In this study, magnesium aluminum layered double hydroxide (MgAl-LDH) was synthesized by two methods: standard coprecipitation and urea hydrolysis. Their textural properties and morphologies were examined by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), thermogravimetry (TG) and differential (DTG) analysis, and point of zero charge (pHpzc). The specific surface area was calculated from BET adsorption equation. The results indicated that the crystallinity and the regularity of the samples prepared by urea hydrolysis were much preferable to those prepared by the coprecipitation method. Their sorption properties toward phosphate were investigated and the experimental evidence showed that, at the initial concentration of 100 mg L-1 and at room temperature, the LDH synthesized by urea hydrolysis had a percentage removal of 94.3 ± 1.12% toward phosphate ions while 74.1 ± 1.34% were uptaked by LDH synthesized by coprecipitation method, suggesting that the crystallinity affects the sorption capability. The sorption mechanism indicates that phosphate ions could be sorbed onto LDHs via electrostatic attraction, ligand exchange, and ion exchange.