This work reports the modification of West Java natural bentonite as an effective adsorbent for rhodamine B dye. The modification was finished by sodium intercalation at room temperature to get low-energy preparation. Characterization of bentonite-modified adsorbent was used SEM, XRD, FTIR, and BET analysis. The material pore size and surface area were increased by 0.303 nm and 178.710 m2/g on Na-bentonite. The adsorption mechanism conformed well with the Freundlich isotherm model and pseudo-second-order kinetics equations. The adsorption process by thermodynamic analysis was endothermic and advantageous. Under the optimum condition of pH 6 (confirmed by pHpzc), initial dye concentration of 125 mg/L, and the adsorbent dosage of 0.09 g for 65 minutes, the Na-bentonite has a larger adsorption capacity (Qm) of 142.86 mg/g, while the different adsorbent dosages of 0.11 g for 75 minutes, the adsorption capacity of natural bentonite (Qm) reaches 140.85 mg/g. This work provides a method for establishing a low-energy preparation adsorbent of bentonite-based on Na intercalant as a low-cost and valuable adsorbent for waste dye removal.
Modification of Java bentonite assists by the multi-step intercalation of sodium and ammonium ions under lowtemperature preparation. The adsorbent was examined to remove rhodamine B and methylene blue dyes in an aqueous solvent. The analysis of structural changes conducted by XRD analysis showed the peak shifting from 19.89° to 16.1° and specific peak spectra FTIR of 2846.93 cm -1 due to increase basal spacing from ammonium intercalation. The total capacities of NH-bentonite, Na-bentonite, and Natural Bentonite adsorption to rhodamine B were 192.308 mg/g, 136.936 mg/g, and 116.279 mg/g, respectively, under acidic conditions. Furthermore, the total capacities of NH-bentonite, Na-bentonite, and Natural Bentonite adsorption to methylene blue were 270.27 mg/g, 158.73 mg/g, and 136.986 mg/g, respectively, under alkaline conditions. The adsorption mechanism described that the rhodamine B and methylene blue removal occurred endothermically, was feasible, and adhered to the kinetics model of pseudo-second-order and Langmuir isotherm. It concluded that the modified Java Bentonite from multistep intercalation is affordable and effective as wastewater treatment.
In this work, the Sumatera bentonite was sodium-pillarized in a new low-temperature and restricted time preparation route and then applied in anionic surfactant sodium lauryl sulphate removal. Structure characterization used Fourier Transform Infra Red (FT-IR), Scanning Electron Microscope - Energy Dispersive X-ray (SEM-EDX), X-ray Diffraction (XRD), and Brunauer–Emmett–Teller (BET) analysis. A strong peak at 22° and 35.66° in XRD analysis was detected as Sodium-pillar that increased crystallinity, then the functional changes of dehydration in lattice structure were detected in 1013 cm−1 by FTIR analysis. The morphology and compositional transformation were analyzed by SEM-EDX and BET analysis, denoted by increasing particle shape and sodium intercalant composition homogeneity. Moreover, the surface area increased from 61.791 to 66.086 m2/g. The sodium lauryl sulphate adsorption by bentonite-Na reached maximum capacity at 8.403 mg/g, which is higher than the pristine bentonite (5.747 mg/g) under the optimum condition. The adsorption mechanism is feasible, endothermic, and conformed to the pseudo-second-order and Freundlich adsorption model. The new route proposed for sodium intercalation effectively improves the Sumatera bentonite adsorption ability to remove sodium lauryl sulphate waste. Copyright © 2023 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
The layered double hydroxide-based material features of Ca/Al have improved according to the adsorption capacity and structure stabilization by transforming into composite Ca/Al-graphite. The composite was synthesized by co-precipitation method, and the chemical structure was characterized using X-ray Diffraction (XRD), Fourier Transform Infra-red (FT-IR), Brunauer Emmet-Teller (BET) Surface Area, and Thermo-Gravimetry Differential Analyse (TG-DTA). The XRD analysis of Ca/Al-Graphite composite was noticed in 10.205°(003), 18.083°(012), 20.45°(004), 26.532°(002), 44.52°(101), 54.52°(004), and 77.38°(006). The TG-DTA analysis of the composite was noticed at 100°C as water molecule decomposition, 270°C as nitrate decomposition, and 700 and 760°C as graphite decomposition to the oxide form. BET surface area analysis of Ca/Al-Graphite composite achieved the highest surface area at 16.795 m2/g. According to the kinetic parameter, the adsorption of direct orange to composite follows the pseudo-second-order model. The isotherm parameter of direct orange adsorption onto the composite followed the Langmuir model and occurred spontaneously and endothermically. The regeneration study proved the composite effective in 3 cycles by adsorption percentage at the third cycle reached 73.559%.
Clay intercalation has been completed to improve coagulation ability using ammonium ions intercalant via multi-step intercalation. The intercalated clay was confirmed by Scanning Electron Microscope-Energy Dispersive Spectroscopy analysis of expanded lamellar and reduction impurities. Fourier Transform Infra-Red analysis confirmed the sharp and strong peak adsorption at 1448 cm-1 as ammonium (NH4+) bendingvibration, and X-Ray Diffraction analysis confirmed the peak shifting to smaller 2? at 10.08° as increasing basal spacing because of ammonium ion intercalated. The Palm Oil Mill Effluent (POME) coagulation was carried out using contact time and coagulant dose variations to determine the optimum conditions, reaching 45 minutes of coagulation and 0.4 g coagulant was used. Furthermore, the turbidity, free fatty acid, and total suspended solids were measured to reach the reduction values of 93%, 49.7%, and 73.7%, respectively. The reusable study of ammoniumintercalated clay confirmed the stability of the three cycles of coagulation used.
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