Amputation of Remazol brilliant blue dye on crosslinked chitosan hydrogel: Statistical treatment and experimental evaluation.

The primary aim of this research is to comprehensively assess the applicability of chitosan biopolymer towards water treatment application and to enhance its adsorption capacity towards Remazol brilliant blue R-19 dye. This has been achieved through physical modification to obtain the material in hydrogel form and chemical modification by crosslinking it with barbituric acid. The characterization of the resulting Chitosan-barbituric acid hydrogel (CBH) was carried out using various analytical techniques such as SEM-EDX, FT-IR, TGA-DTA, XRD, and BET. CBH was employed as the adsorbent to eliminate R-19 dye from aqueous media. Utilizing response surface methodology (RSM), the parameters were fine-tuned, leading to the achievement of more than a 95% removal for R-19 dye. The adsorption behavior closely adhered to the Langmuir isotherm and pseudo-second-order kinetics. An interesting observation indicated that the rise in temperature leads to rise in adsorption capacity of CBH. The maximum adsorption capacities evaluated at 301.15 K, 313.15 K, 318.15 K, and 323.15 K were 566.6 mg g-1, 624.7 mg g-1, 671.3 mg g-1, and 713.5 mg g-1 respectively, in accordance with the Langmuir isotherm model. Examining the thermodynamics of the adsorption process revealed its spontaneous nature (ΔG = -21.14 to -27.09 kJ mol-1) across the entire temperature range. Furthermore, the assessment of the isosteric heat of adsorption (ΔHads) was conducted using the Clausius-Clapeyron equation, with results indicating an increase in ΔHads from 1.85 to 2.16 kJ mol-1 with temperature rise from 301.15 K to 323.15 K due to augmented surface loading. This suggested the existence of lateral interactions between the adsorbed dye molecules. The potential of adsorbent for regeneration was investigated, demonstrating the ability to reuse the material. Sustainability parameter calculated for synthesis process reflected a notably low E-factor value of 0.32 demonstrated the synthesis is environment friendly.

Highly efficient mesoporous aluminium-magnetite-alginate magnetic composite for defluoridation of water.

One of the few elements that can have negative health impacts in both conditions, when consumed in excess or insufficiency is fluoride. In current study, aluminium magnetite alginate composite (AMA) was fabricated and applied using batch adsorption of fluoride as well as by using statistical modelling. Heterogeneous surface as revealed from scanning electron micrograph, thermal stability shown by thermal studies, high surface area of 29.77 m2 g-1, pore volume 0.1987 cm3 g-1 with mesoporous structure having average pore radius of 133 Å shown by BET analysis, fare degree of magnetization from VSM analysis were the important features of this material. Screening experiments and batch trials were carried out to obtain optimum working conditions. pH of 3.0, dosage of 50 mg, interaction period of 60 min and concentration of 50 mg L-1 depicted maximum defluoridation efficacy of about 94%. The adsorption capacity was found to be 60.08 mg g-1 in accordance with Langmuir adsorption isotherm, while pseudo second order kinetics was followed. Overall effects of various factors on sorption process were optimized using response surface methodology (RSM). Regeneration potential of AMA has been demonstrated for 10 adsorption-desorption cycles, showing more than 60% efficiency in tenth cycle. The AMA composite shows E-factor value 0.004 depicting it is sustainable in environment. In short, this novel composite showed excellent morphological, magnetic, functional properties that led to enhanced adsorption efficiency in short span of time that can be regenerated and reused in multiple cycles.

Efficient multi-ion adsorption using chitosan-malonic acid film: Enhancement using response surface methodology.

The objective of this research is to conduct a comprehensive characterization of chitosan while also improving its attributes by crosslinking with malonic acid, with a focus on its efficacy in removing hexavalent chromium, arsenite and fluoride ions. Crosslinking chitosan in 1:0.5 mass ratio forming a film led to substantial enhancement in confiscation of these target pollutants. The characterization of the adsorbent involved several techniques, including FT-IR, TGA-DSC, SEM-EDX, XRD, and BET surface area analysis. In batch adsorption experiments, Chitosan-malonic acid (CMA) was employed to remove CrVI, AsIII and F- from aqueous solutions. These experiments were conducted while varying conditions such as pH, dosage, concentration, temperature, and time. Through the implementation of response surface methodology (RSM), parameters were optimized, resulting in over 95% removal of CrVI, AsIII and F- ions. The isotherm and kinetics data demonstrated a good fit with the Langmuir isotherm model and pseudo second-order kinetics, respectively. According to the Langmuir isotherm, the maximum adsorption capacities on CMA for CrVI, AsIII and F- were determined to be 687.05 mg g-1, 26.72 mg g-1 and 51.38 mg g-1 respectively under optimum pH of 4.0, 7.0 and 5.0 respectively under ambient temperature of 303 K. Thermodynamic analysis indicated that the adsorption process was spontaneous and driven by enthalpy. The regenerability of the adsorbent was validated through five adsorption-desorption cycles, signifying its reusability. An assessment of the adsorbent's sustainability indicated an eco-friendly synthesis, as reflected by the low E-factor value of 0.0028.

Novel Chitosan-ZnO nanocomposites derived from Nymphaeaceae fronds for highly efficient removal of Reactive Blue 19, Reactive Orange 16, and Congo Red dyes.

The primary aim of this investigation was to synthesise novel adsorbent by incorporating greenly synthesized zinc oxide nanoparticles into chitosan matrix (G-ZnO-Cs). The production of ZnO Nanoparticles via a green approach involved the utilization of extracts derived from Nymphaeaceae fronds. This assertion was substantiated by the application of Field Emission Scanning Electron Microscopy (FESEM) and X-ray Diffraction (XRD) analytical techniques. Several Analytical methods such as Fourier Transform Infrared spectroscopy (FT-IR), Energy Dispersive X-ray Analysis (EDAX), FESEM, Thermogravimetric Analysis (TGA), XRD, Brunauer-Emmett-Teller (BET) analysis, and point-of-zero charge determination were used to characterize G-ZnO-Cs. Further study investigates the impact of five key processing parameters, namely pH, interaction duration, G-ZnO-Cs dosage, temperature, and initial concentration of dyes, on the removal of three organic dyes Reactive Blue 19 (RB 19), Reactive Orange 16 (RO 16), and Congo Red (CR) The adsorption process of Reactive Blue 19 (RB 19), Reactive Orange 16 (RO 16), and Congo Red (CR) dyes on G-ZnO-Cs were determined to comply to the pseudo-second-order (PSO) and Langmuir models, as determined through equilibrium and kinetic experiments. The highest adsorption capabilities for RB 19, RO 16 and CR dye were revealed to be 219.6 mg/g, 129.6 mg/g, and 118.8 mg/g, respectively. The elimination success rate of the fixed-bed column approach for treating huge volumes was highlighted in the conducted research. Moreover, the G-ZnO-Cs composite exhibited significant reusability due to its ability to undergo elution and simultaneous regeneration processes.

Dual modifications of chitosan with PLK for amputation of cyanide ions: Equilibrium studies and optimization using RSM.

The aim of the study is to characterize and hierarchically modify chitosan using partially lateritized khondalite (PLK) rock. PLK is a metamorphic rock rich in mineral oxides and is not commercialized thus, treated as a mining reject. Chitosan was sequentially altered to Chitosan-PLK (Ch-PLK) and Chitosan-PLK-Epichlorohydrin (Ch-PLK-ECH) and both the materials were characterized by FT-IR, SEM, EDX, XRD, XRF and BET surface area analysis. The adsorbents were used for removal of cyanide ions from aqueous solution using batch adsorption experiments. The experiments were performed varying operational parameters and were optimized using RSM. The conditions optimized by RSM were carried out, more than 90 % of CN- adsorption was observed. The isotherm and kinetics studies have shown that the adsorption process fitted well with Langmuir isotherm model and pseudo second order kinetics. Using Langmuir isotherm, the maximum adsorption capacities of Ch-PLK and Ch-PLK-ECH towards cyanide ions at 30 °C were found to be 23.98 mg g-1 and 65.27 mg g-1 respectively. Thermodynamic studies described that adsorption process was spontaneous, enthalpy-driven over entire temperature range. Column studies established that the adsorbents may be applicable to large volume of samples. The adsorbents were tested for regeneration for 5 adsorption-desorption cycles suggesting reusability of the materials.