The performance of calcined serpentine to simultaneously remove fluoride, iron and manganese

To solve the problem of high fluoride, iron and manganese concentrations in groundwater, serpentine (Srp) was modified by metal salt impregnation, acid-base activation and calcination, and the effects of these three modifications on removal performance of Srp were compared. Specifically, the effects of the calcined serpentine (Csrp) dose, reaction time, pH, and temperature on the removal performance of F−, Fe2+ and Mn2+ on Csrp were analysed. An isothermal adsorption model and adsorption kinetic equation were established and confirmed through SEM, EDS, XRD and FTIR spectroscopy to analyse the mechanism of removing F−, Fe2+ and Mn2+ by Csrp. The results show that when 3 g/L Csrp was used to treat water samples with 5 mg/L F−, 20 mg/L Fe2+, and 5 mg/L Mn2+ (pH of 6, reaction temperature of 35 °C, and time of 150 min), the removal rates of F−, Fe2+, and Mn2+ were 94.3%, 99.0%, 98.9%, respectively. The adsorption of F−, Fe2+ and Mn2+ on Csrp follows the quasi-second-order kinetic equation and Langmuir isotherm adsorption model. After 5 cycles of regeneration of Csrp, Csrp can still maintain good properties of fluoride,iron and manganese removal.

Isotherm study of banana stem waste adsorbents to reduce the concentration of textile dying waste

The purpose of this study was to make carbon from banana stem waste and determine the isotherm adsorption characteristics of carbon from banana stem waste to methyl orange compounds. The process for making carbon from banana stem waste was done through the stages of preparation and carbonization at a temperature of 250°C for 1.5 h. Before being used as carbon, banana stem waste was cleaned, washed, dried, and mashed using a mill. The carbon then went through a washing process to remove impurities and tested for its absorbance ability into a solution containing a methyl orange compound under constant conditions of pH, temperature, and pressure. The experimental results showed that the appropriate sequence of adsorption models is the Langmuir, Temkin, Freundlich, and Dubinin-Radushkevich models. Adsorption occurs on the surface of a single layer (monolayer) and the interaction between the adsorbent and the adsorbate occurs physically. The value of maximum adsorption capacity (Qmax) is 37.5940 mg/g. The presence of banana stem carbon is expected to reduce the negative impacts, one of which is the disposal of industrial wastewater from textile factories.

The Production of Green Diesel Rich Pentadecane (C15) from Catalytic Hydrodeoxygenation of Waste Cooking Oil using Ni/Al2O3-ZrO2 and Ni/SiO2-ZrO2

Hydrodeoxygenation (HDO) is applied in fuel processing technology to convert bio-oils to green diesel with metal-based catalysts. The major challenges to this process are feedstock, catalyst preparation, and the production of oxygen-free diesel fuel. In this study, we aimed to synthesize Ni catalysts supported on silica-zirconia and alumina-zirconia binary oxides and evaluated their catalytic activity for waste cooking oil (WCO) hydrodeoxygenation to green diesel. Ni/Al2O3-ZrO2 and Ni/SiO2-ZrO2 were synthesized by wet-impregnation and hydrodeoxygenation of WCO was done using a modified batch reactor. The catalysts were characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), and scanning electron microscopy - energy dispersive X-ray spectroscopy (SEM-EDS), and N2 isotherm adsorption-desorption analysis. Gas chromatography - mass spectrometry (GC-MS) analysis showed the formation of hydrocarbon framework n-C15 generated from the use of Ni/Al2O3-ZrO2 with the selectivity of 68.97% after a 2 h reaction. Prolonged reaction into 4 h, decreased the selectivity to 58.69%. Ni/SiO2-ZrO2 catalyst at 2 h showed selectivity of 55.39% to n-C15. Conversely, it was observed that the reaction for 4 h increased selectivity to 65.13%. Overall, Ni/Al2O3-ZrO2 and Ni/SiO2-ZrO2 catalysts produced oxygen-free green diesel range (n-C14-C18) enriched with n-C15 hydrocarbon. Reaction time influenced the selectivity to n-C15 hydrocarbon. Both catalysts showed promising hydrodeoxygenation activity via the hydrodecarboxylation pathway. Copyright © 2021 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).

Preparation of Magnetic Composite Polyaniline/Fe3O4−Hydrotalcite and Performance in Removal of Methyl Orange

Magnetic composite fabricated from polyaniline and Fe3O4-hydrotalcite (Pan/MHT) was successfully applicated for removal of methyl orange (MO) from wastewater. The structure and properties of Pan/MHT were characterized by Fourier-transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction, vibrating sample magnetometer, and Brunauer-Emmett-Teller adsorption isotherm. Adsorption kinetic results indicated that the adsorption process followed pseudosecond-order kinetic model ( R 2 = 0.999 ), MO adsorption onto Pan/MHT was well described by Freundlich isotherm ( R 2 = 0.994 ), and the MO adsorption capacity of 2 Pan/MHT obtained the highest with Q e = 156.25 mg / g . Batch adsorption experiments were carried out using magnetic composite with the effects of initial MO concentration, solution pH, and adsorbent dosage. The results revealed that the magnetic Pan/MHT exhibited efficient adsorption of MO in the aqueous solution as a result of the affinity for organic dyes, microporous structure, and suitable surface area for adsorption (15,460 m2/g). The superparamagnetic behavior of Pan/MHT (with H c = 18.56 Oe , M s = 23.38 × 10 − 3 emu / g , and M r = 0.91 × 10 − 3 emu / g ) helps that it could be separated from the solution and performs as an economical and alternative adsorbent to removal and degrade azo dye from wastewater. Pan/MHT was also investigated to reuse after desorption of MO in 0.1 M HCl, and the results show that 2 Pan/MHT can be reused for 4 cycles with Q e = 79.66 mg / g .

Synthesis, characterization, and evaluation of ZrSiO4/Fe2O3 adsorbent for methylene blue removal in aqueous solutions

Methylene blue dyes are widely used in textile, batik, plastic, paper, and many other industries. The remain of methylene blue dyes in the textile waste is hazardous for health and the environment. Therefore, it takes effort to deal with it. One of the efforts is the process of adsorption using adsorbents. In this study, the adsorbent ZrSiO4/Fe2O3 was synthesized using the coprecipitation method using NaOH as precipitant. Either ZrSiO4 or Fe2O3 was synthesized from Indonesia mineral local zircon sand and jarosites, respectively. The composites of ZrSiO4/Fe2O3 were prepared in %mole variation, which is 75:25; 50:50; and 25:75. All obtained composites were then characterized using X-Ray Diffraction (XRD). The XRD analysis showed that the crystal structure formed was tetragonal for ZrSiO4 and hexagonal for Fe2O3 (also known as α-Fe2O3). Evaluation toward isotherm adsorption and kinetic adsorption showed that the adsorption of MB using ZrSiO4/Fe2O3 follows the Langmuir isotherm model and pseudo-second-order model, respectively.

Synthesis and Characteristic Properties of Crosslinked Chitosan with Epichlorohydrin for Nitrate Removal from Water

In this study, we prepared chitosan beads cross-linked with epichlorohydrin (CB-ECH) to improve the removal of nitrate in groundwater. It was confirmed that CB-ECH exhibited higher thermal stability and well-developed nano-pores compared to the pure chitosan beads (CB) by the thermogravimetric analyzer, nitrogen gas adsorption and desorption isotherm, and field emission scanning microscopy analysis. The CB-ECH showed a higher nitrate adsorption amount than the pure CB. Nitrate adsorption behaviors of CB-ECH were further investigated using adsorption isotherm, adsorption kinetics, adsorption energy distribution, and Gibbs free energy distribution models. The adsorption equilibrium and kinetics of nitrate ion on CB-ECH were well explained by the Sips isotherm and homogeneous surface diffusion model, respectively. It was also found from the AED analysis that the CB-ECH represent the heterogeneous adsorption behaviors for nitrate.

The adsorption characteristics of Cu(II) and Zn(II) on the sediments at the mouth of a typical urban polluted river in Dianchi Lake: taking Xinhe as an example

This study is to determine the spatial distribution characteristics of Cu and Zn adsorption on the sediments of the estuary of Dianchi Lake, as well as the composite adsorption law of Cu and Zn on combinations of sediment organic matter, metal oxides, and organic–inorganic composites. The relationship between the adsorption contribution of each component of the substance. A static adsorption experiment was applied to the sediments in the estuary of Dianchi Lake. The relationship between adsorption capacity and sediment composition was analyzed through correlation analysis and redundant analysis. The results show that along the direction of the river flow and the vertical depth, the adsorption capacity presents a relatively obvious spatial distribution law; the change trend of sediment component content is not the same as the change trend of Cu and Zn adsorption capacity. The change trend of the sediment component content is not the same as the change trend of the adsorption amount of Cu and Zn, and the compound effect between the components affects the adsorption amount. The adsorption of Cu by the four groups of sediments after different treatments is more in line with the Freundlich isotherm adsorption model; When adsorbing Zn, the untreated and removed organic matter and iron-aluminum oxide group are in good agreement with the Freundlich model, while the organic matter-removed group and the iron-aluminum oxide removal group are more consistent with the Langmuir isotherm adsorption model; The adsorption contribution rate of organic–inorganic composites in sediments is not a simple addition of organic matter and iron-aluminum oxides, but a more complex quantitative relationship.

Modification of Cu/Cr Layered Double Hydroxide by Keggin Type Polyoxometalate as Adsorbent of Malachite Green from Aqueous Solution

Modification of Cu/Cr layered double hydroxides (LDHs) has been conducted by intercalation using Keggin type polyoxometalate [a-SiW12O40]4- to form CuCr-[a-SiW12O40]. The materials were analyzed by XRD, FTIR, and surface area analyses. Furthermore, materials were used as selectivity adsorbents of cationic dyes such as malachite green, rhodamine-B and methylene blue. The malachite green is more selective than others from an aqueous solution. The adsorption of malachite green showed that the adsorption capacity of CuCr-[a-SiW12O40] was higher than pristine LDHs. The adsorption process was followed pseudo second order kinetic model and Langmuir isotherm adsorption. The Qmax value of CuCr-[a-SiW12O40] reached 55.322 mg/g at 323 K after 100 minutes adsorption time. Thermodynamic parameters such as ΔG, ΔH and ΔS confirm that the adsorption process was endothermic, spontaneous, and more favorable at high temperatures. The intercalated material was higher structural stability toward reusability adsorbent than pristine LDHs.

Efficient trapping of cesium ions in water by titanate nanosheets: experimental and theoretical studies

In recent years, TNS has attracted wide attention because of its simplicity in synthesis and high efficiency in ion exchange. The adsorption of cesium ions in aqueous solution by TNS was investigated in this stud. Results show that the removal rate of Cs (I) is about 88% when pH = 5.00 ± 0.05, C0 = 10 ppm and CTNS = 0.1 g/L. The adsorption equilibrium is reached in about 20 minutes and best fits pseudo-second order model, R2 = 0.9998; Compared with the Freundlich isotherm adsorption model and Temkin model, the Langmuir model has the best fitting effect, R2 = 0.9903. The fitting results show the maximum adsorption capacity of TNS for Cs (I) is 200.00 mg/g. The main adsorption mechanism of TNS to cesium ion is ion exchange. Therefore, TNS can be used as a potential adsorbent for effectively adsorbing Cs-containing wastewater.