Removal of Cr(VI) from the aqueous phase using numerous activated carbons (AC) has been broadly studied in the last decades. Nevertheless, the diversity of activation methods, AC properties, and adsorption conditions precludes the standardization of specific characteristics required to achieve better adsorption results. This work reviewed the pertinent literature on Cr(VI) adsorption onto AC published over the past four decades. Pearson's correlation matrix and principal component analysis (PCA) assisted in identifying the parameters and AC characteristics that have the greatest influence on the maximum adsorption capacity (q). Two hundred thirty-six adsorption assays were found reporting data on 110 ACs and different parameters. Of these, 39.8% of the studies contemplated the variables q, pH, temperature (T), surface area (S), micropore volume (V), and mesopore volume (V), and only 19.5% reported the point of zero charge (pH). Statistical analysis disclosed that S and V have a strong positive correlation with q, while V, T, and pH show little or no correlation. The difference between pH and pH (PZC) indicated a significant anticorrelation with q, thus evidencing that lower PZC values enhance adsorption. The findings are useful for all researchers that work with Cr(VI) adsorption on AC since they provide a start point concerning the required adsorbent characteristics and process conditions to be employed.
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Macromol Rapid Commun
December 2024
Hunan Key Laboratory of Micro & Nano Materials Interface Science, College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, China.
The CO-epoxide addition to cyclic carbonate is of great significance but usually requires high temperatures and CO pressures. Herein, a spirobifluorene-based porous organic polymer catalyst is designed with a Co-salen complex immobilized on the backbone (ST-CoSalen-POP) to enable CO fixation under mild conditions. ST-CoSalen-POP possesses a high Co-loading content (9.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
Department of Chemistry, Southern University of Science and Technology, Shenzhen 518055, Guangdong, China.
The electrochemical reduction reaction (RR) of CO to high value multicarbon products is highly desirable for carbon utilization. Dual transition metal atoms dispersed by N-doped graphene are able to be highly efficient catalysts for this process due to the synergy of the bimetallic sites for C-C coupling. In this work, we screened homonuclear dual-atom catalysts dispersed by N-doped graphene to investigate the potential in CO reduction to C products by employing density functional theory calculations.
View Article and Find Full Text PDFSmall
December 2024
College of Electronic and Optical Engineering & College of Flexible Electronics (Future Technology) & State Key Laboratory of Organic Electronics and Information Displays, Nanjing University of Posts and Telecommunications (NJUPT), Nanjing, 210023, P. R. China.
In the era of atomic manufacturing, the precise manipulation of atomic structures to engineer highly active catalytic sites has become a central focus in catalysis research. Dual-atom catalysts (DACs) have garnered significant attention for their superior activity, selectivity, and stability compared to single-atom catalysts (SACs). However, a comprehensive review that integrates geometric and electronic factors influencing DAC performance remains limited.
View Article and Find Full Text PDFInt J Phytoremediation
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Department of Ecology, Jinan University, Guangzhou, China.
Vegetated ditches have been demonstrated to be an effective method for pollutant remediation. This study assesses the removal potential and pathways for herbicide runoff pollution utilizing , , , and ditches. Resultes show these vegetated ditches significantly outperform unvegetated ones in removing atrazine and diuron during runoff events ( < 0.
View Article and Find Full Text PDFLangmuir
December 2024
School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, P. R. China.
This study explores the bubble nucleation process and heat transfer characteristics on nanostructured solid surfaces with mixed-wettable pillars using molecular dynamics simulations. Five different surfaces were designed by varying the wettability of the central pillars while keeping the lateral pillars hydrophilic. The nucleation behavior of argon bubbles was observed to differ significantly across these surfaces due to the combined effects of nanostructuring and mixed wettability.
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