In this study, carboxymethyl cellulose based graft poly(acrylamide) hydrogel (CMC-g-P(AAm)) and its nanocomposite with montmorillonite (CMC-g-P(AAm)/MMT) were produced by the free radical method and it was used to malachite green (MG) dye removal from aqueous solution. The properties and characterization of the adsorbents were investigated using FTIR, SEM, TGA, and XRD analyzes, and the results showed that MMT nanoparticles were successfully distributed in the hydrogel system. MMT nanoparticles were loaded into the hydrogel system with different weight percentages and the maximum adsorption efficiency of MG dye was determined at 10 wt% MMT. Also, the effect of temperature, contact time, initial concentration of MG dye and initial pH on the adsorption efficiency of MG dye was studied in a batch. Equilibrium behavior investigation of the adsorption process showed that the equilibrium data determined are in good agreement with the Langmuir isotherm model and the monolayer surfaces play an effective role in the adsorption process. The maximum monolayer adsorption capacity (q) determined using the Langmuir isotherm model for CMC-g-P(AAm) and CMC-g-P(AAm)/MMT were determined to be 158.1 mg/g and 172.4 mg/g, respectively. Also, the kinetic study showed that the pseudo-second- order kinetic model is more capable of describing the kinetic behavior of the process than other models. Also, the α parameter values for the MG dye adsorption process using CMC-g-P(AAm) and CMC-g-P(AAm)/MMT were determined to be 0.6337 mg/g·min and 31.04 mg/g·min, respectively. This indicates that the produced composite has a high adsorption value. Gibbs free energy (ΔG°) was negative for the adsorption processes in the range of 25-50 °C, indicating that the process was spontaneous. In addition, the enthalpy parameter (ΔH°) was determined for the adsorption process using CMC-g-P(AAm) and CMC-g-P(AAm)/MMT nanocomposite hydrogels at 39.859 KJ/mol and 74.736 KJ/mol, respectively. Positive ΔH° indicates that the process is endothermic in the range of 25-50 °C using both adsorbents. Also, the concentrations effect of Na+ and K+ ions on adsorption efficiency was investigated and it was concluded that the efficiency of the adsorption process decreased with the increase of ions concentration. Adsorption efficiency decrease can be due to the occupation of active sites and repulsive electrostatic interactions at the adsorbent surface with the MG dye molecule.
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http://dx.doi.org/10.1016/j.ijbiomac.2020.05.093 | DOI Listing |
Adv Mater
January 2025
Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong, SAR, 999077, P. R. China.
Electrochemically converting nitrate (NO ) to value-added ammonia (NH) is a complex process involving an eight-electron transfer and numerous intermediates, presenting a significant challenge for optimization. A multi-elemental synergy strategy to regulate the local electronic structure at the atomic level is proposed, creating a broad adsorption energy landscape in high-entropy alloy (HEA) catalysts. This approach enables optimal adsorption and desorption of various intermediates, effectively overcoming energy-scaling limitations for efficient NH electrosynthesis.
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January 2025
Institute for Sustainable Energy and Resources, Key Laboratory of Shandong Provincial Universities for Functional Molecules and Materials, College of Chemistry and Chemical Engineering, Qingdao University, Qingdao, Shandong, 266071, China.
Alkaline water (HO) electrolysis is currently a commercialized green hydrogen (H) production technology, yet the unsatisfactory hydrogen evolution reaction (HER) performance severely limits its energy conversion efficiency and cost reduction. Herein, PtRuFeCoNi high entropy alloys (HEAs) is synthesized and subsequently exploited electrochemically induced structural oxidation processes to construct self-reconfigurable HEAs, as an efficient alkaline HER catalyst. The optimized self-reconstructed PtRuFeCoNi HEAs with the HEAs and cobalt rutheniate interface (HEAs-CoRuO) exhibits excellent alkaline HER performance, requiring just 11.
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January 2025
School of Energy Science and Engineering, Indian Institute of Technology Kharagpur, Kharagpur, 721302, India.
Inducing magnetic ordering in a non-ferrous layered double hydroxides (LDHs) instigates higher spin polarization, which leads to enhanced efficiency during oxygen evolution reaction (OER). In nano-sized magnetic materials, the concept of elongated grains drives domain alignment under the application of an external magnetic field. Hence, near the solid electrode interface, modified magnetohydrodynamics (MHD) positively impacts the electrocatalytic ability of non-ferrous nanocatalysts.
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January 2025
School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai, 200093, P. R. China.
Chlorophenols are difficult to degrade and mineralize by traditional advanced oxidation processes due to the strong electronegativity of chlorine. Here, a dual-site atomically dispersed catalyst (FeMoNC) is reported, which Fe/Mo supported on mesoporous nitrogen-doped carbon is prepared through high-temperature migration. The FeMoNC exhibits a high dechlorination rate of 93.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
January 2025
Departament de Ciència de Materials i Química Física & Institut de Química Teòrica i Computacional (IQTCUB), Universitat de Barcelona, c/Martí i Franquès 1-11, 08028 Barcelona, Spain.
First-principles density functional theory calculations are carried out on the (TiO) cluster supported on the TiCT (0001) surface with different chemical terminations, , -H, -O, and -OH, to study the interaction and understand the TiCT functionalization effect on the formation of (TiO)/TiCT composites. Results show an exothermic interaction for all cases, whose strength is driven by the surface termination, promoting weaker bonds when the MXene is functionalized with H atoms. For TiCH and TiC(OH) MXenes, the interaction is accompanied by a charge transfer towards the titania cluster.
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