In the present study, the gel anion exchanger Purolite A-850 of N(+)(CH(3))(3) functional groups was used in order to remove the acidic dye (Acid Blue 29) from aqueous solutions. Batch experiments were conducted to study the effect of phase contact time (1-180 min), initial concentration of dye (100-500 mg/L), solution pH (1-8), anion exchanger dosage (0.25-1.0 g) as well as temperature (20-40 degrees C). The contact time necessary to reach equilibrium was 40 min with the exception for the solution of the initial concentration 500 mg/L. The amounts of Acid Blue 29 adsorbed at equilibrium using the strongly basic anion exchanger were equal to 9.97, 19.97, 29.96 and 49.90 mg/g for the dye solutions of the initial concentrations 100, 200, 300 and 500 mg/L, respectively. The equilibrium sorption capacity slightly increased when the temperature of dye solution increased from 20 to 40 degrees C. The experimental data were analyzed by the Langmuir, Freundlich and Temkin models of adsorption. The adsorption isotherm data were fitted well to the Langmuir isotherm and the monolayer adsorption capacity was found to be 83.303 mg/g at 20 degrees C. The value of R(L) was equal to 0.00054 (favourable). The kinetic data obtained at different concentrations were modeled using the pseudo-first order, pseudo-second order and intraparticle diffusion equations. The experimental data were well described by the pseudo-second order kinetic model.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.jhazmat.2009.07.069 | DOI Listing |
Glob Chang Biol
January 2025
Department of Civil, Environmental, and Geo-Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
Stomata control plant water loss and photosynthetic carbon gain. Developing more generalized and accurate stomatal models is essential for earth system models and predicting responses under novel environmental conditions associated with global change. Plant optimality theories offer one promising approach, but most such theories assume that stomatal conductance maximizes photosynthetic net carbon assimilation subject to some cost or constraint of water.
View Article and Find Full Text PDFRSC Adv
January 2025
Centre for Advanced Materials and Devices (CAMD), Department of Chemistry, Faculty of Science, University of Colombo Colombo Sri Lanka
The global scarcity of irrigation-grade water poses severe concerns in the agricultural sector. Desalination techniques including reverse osmosis, electrodialysis, capacitive deionization, membrane filtration, and multi-stage flash are some dynamic solutions to mitigate this challenge. In this study, novel bio-filter materials were explored and developed for the application of membrane-based electrodialysis.
View Article and Find Full Text PDFPhotosynth Res
January 2025
Research Institute for Interdisciplinary Science and Graduate School of Natural Science and Technology, Okayama University, Okayama, 700-8530, Japan.
Red algae are photosynthetic eukaryotes whose light-harvesting complexes (LHCs) associate with photosystem I (PSI). In this study, we examined characteristics of PSI-LHCI, PSI, and LHCI isolated from the red alga Galdieria sulphuraria NIES-3638. The PSI-LHCI supercomplexes were purified using anion-exchange chromatography followed by hydrophobic-interaction chromatography, and finally by trehalose density gradient centrifugation.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education, Institute of New-Energy, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China.
The development of water splitting technology in alkaline medium requires the exploration of electrocatalysts superior to Pt/C to boost the alkaline hydrogen evolution reaction (HER). Ruthenium oxides with strong water dissociation ability are promising candidates; however, the lack of hydrogen combination sites immensely limits their performance. Herein, we reported a unique RuO catalyst with metallic Ru on its surface through a simple cation exchange method.
View Article and Find Full Text PDFChemistry
January 2025
Jadavpur University, Chemistry, 188 Raja S. C. Mallick Road, 700032, Kolkata, INDIA.
Two π-radical complexes containing bisazo-aromatic-centered radical anion (1•-) were synthesized through in-situ electron transfer from metal-to-ligand using [IrI] and 2-(2-Pyridylazo)azobenzene (1) in inert hydrocarbon solvent. These are characterized as diradical [IrIII(1•-)2]+[2]+ and monoradical [IrIII(1•-)Cl2(PPh3)] 3. In contrast, a rare metal-mediated hydrolytic cleavage of the C(sp2)-N bond occurred in protic solvent resulting in quaternary radical complex [IrIII(1•-)(1')(PPh3)]+(4)+.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!