Organic dye-containing wastewater has become an increasingly serious environmental problem due to the rapid development of the printing and dyeing industry. Hydrogel is a promising adsorbent for organic dyes because of its unique three-dimension network structure and versatile functional groups. Though many efforts have been made in hydrogel adsorbents recently, there is still a critical challenge to fabricate hydrogel adsorbent with high adsorption capacity and high efficiency at the same time. To address this concern, we developed a calcium hydroxide nano-spherulites/poly(acrylic acid -[2-(Methacryloxy)ethyl]trimethyl ammonium chloride) hydrogel adsorbent with novel villi-like structure. The hydrogels were prepared through a simple free radical copolymerization method using calcium hydroxide nano-spherulites as crosslinker. The resultant hydrogel adsorbents showed a maximum adsorption capacity of 2249 mg/g in a 400 mg/L methylene blue solution and a high removal ratio of 98% in 1 h for a 50 mg/L methylene blue solution. In addition, the adsorption behaviors of our hydrogel adsorbents could be well described by pseudo-second-order kinetic model and Langmuir adsorption isotherm model. Furthermore, this kind of hydrogel adsorbent showed selective adsorption behavior for methylene blue. Altogether, the hydrogel adsorbent developed in this work has a high capacity and high efficiency in organic dye removing and promised a great potential in wastewater treatment application.
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http://dx.doi.org/10.1016/j.jcis.2021.02.124 | DOI Listing |
Polymers (Basel)
January 2025
Department of Chemical and Metallurgical Engineering, School of Chemical Engineering, Aalto University, 02150 Espoo, Finland.
Alginate hydrogels have gathered significant attention in biomedical engineering due to their remarkable biocompatibility, biodegradability, and ability to encapsulate cells and bioactive molecules, but much less has been reported on the kinetics of gelation. Scarce experimental data are available on cross-linked alginates (AL) with bioactive components. The present study addressed a novel method for defining the crosslinking mechanism using rheological measurements for aqueous mixtures of AL and calcium chloride (CaCl) with the presence of hydroxyapatite (HAp) as filler particles.
View Article and Find Full Text PDFGels
January 2025
Ecole Nationale Supérieure de Chimie de Rennes, Univ. Rennes, CNRS, UMR 6226, CEDEX 7, 35708 Rennes, France.
A new green hydrogel consisting of cherry stone (CS) powder and sodium alginate (SA) was synthesized through physical crosslinking. The product had a mean diameter of 3.95 mm, a moisture content of 92.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Chemical Department, Faculty of Science, Damietta University, Damietta 34517, Egypt.
The study investigated the enhancement of stability and efficacy in the removal of bivalent nickel ions (Ni(II)) by utilizing a cerium metal-organic framework (Ce-MOF) encapsulated within a food-grade algal matrix. This composite material is integrated into a dual-layer hydrogel containing chitosan and carboxymethyl cellulose. The enhancement of structural integrity in the final product can be attributed to the cross-linking process with epichlorohydrin, leading to the development of Ce-MOF-FGA/CMC-CS hydrogel beads.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Chemistry and Materials Engineering, Zhejiang A&F University, No. 666 Wusu Street, Hangzhou 311300 PR China. Electronic address:
Developing biomass-based adsorbents with superior uranium uptake performance is imperative yet challenging for the sustainable development of nuclear energy. Herein, we constructed a novel lignin-based adsorbent (DLP@PAO) with dual functional groups and enhanced structural stability via ingenious integration of lignin and polyamidoxime. The two-step modification strategy was innovatively employed to phosphorylate lignin, significantly enhancing the phosphorylation efficiency and achieving an over eight-fold increase in the U(VI) uptake capacity of lignin.
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