Modulation of the driving forces for adsorption on MIL-101 analogues by decoration with sulfonic acid functional groups: superior selective adsorption of hazardous anionic dyes

2020 ◽  
Vol 49 (20) ◽  
pp. 6651-6660
Author(s):  
Ji-Min Yang ◽  
Wei Zhang ◽  
Run-Zhi Zhang ◽  
Meng-Xuan Tong
Keyword(s):  
Functional Groups ◽  
Sulfonic Acid ◽  
Driving Forces ◽  
Selective Adsorption ◽  
Anionic Dyes ◽  
Adsorption Mechanisms ◽  
Adsorption Capacities

MIL-101-SO3H analogues functionalized with –SO3H groups exhibited superior CR, MO and AC adsorption capacities because of their distinct adsorption mechanisms.

scholarly journals Simultaneous removal of cationic and anionic dyes from aqueous solution by double functional groups modified bagasse

2020 ◽  
Vol 82 (10) ◽  
pp. 2159-2167
Author(s):  
Ru-yi Zhou ◽  
Jun-xia Yu ◽  
Ru-an Chi
Keyword(s):  
Aqueous Solution ◽  
Functional Groups ◽  
Order Kinetic ◽  
Anionic Dyes ◽  
Adsorption Capacities ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Amine Groups ◽  
Modified Adsorbents ◽  
Zeta Potential Analysis

Abstract Double functional groups modified bagasse (DFMBs), a series of new zwitterionic groups of carboxyl and amine modified adsorbents, were prepared through grafting tetraethylenepentamine (TEPA) onto the pyromellitic dianhydride (PMDA) modified bagasse using the DCC/DMAP method. DFMBs' ability to simultaneously remove basic magenta (BM, cationic dye) and Congo red (CR, anionic dye) from aqueous solution in single and binary dye systems was investigated. FTIR spectra and Zeta potential analysis results showed that PMDA and TEPA were successfully grafted onto the surface of bagasse, and the ratio of the amount of carboxyl groups and amine groups was controlled by the addition of a dosage of TEPA. Adsorption results showed that adsorption capacities of DFMBs for BM decreased while that for CR increased with the increase of the amount of TEPA in both single and binary dye systems, and BM or CR was absorbed on the modified biosorbents was mainly through electrostatic attraction and hydrogen bond. The adsorption for BM and CR could reach equilibrium within 300 min, both processes were fitted well by the pseudo-second-order kinetic model. The cationic and anionic dyes removal experiment in the binary system showed that DMFBs could be chosen as adsorbents to treat wastewater containing different ratios of cationic and anionic dyes.

Superior adsorptive removal of anionic dyes by MIL-101 analogues: the effect of free carboxylic acid groups in the pore channels

CrystEngComm ◽  
2019 ◽  
Vol 21 (38) ◽  
pp. 5824-5833 ◽  
Author(s):  
Ji-Min Yang ◽  
Run-Zhi Zhang ◽  
Ying-Yan Liu
Keyword(s):  
Carboxylic Acid ◽  
Anionic Dyes ◽  
Adsorption Mechanisms ◽  
Adsorptive Removal ◽  
Carboxylic Acid Groups ◽  
Adsorption Capacities

MIL-101-COOH nanoparticles functionalized with free carboxylic acid groups exhibited superior CR, MO, and AC adsorption capacities via their distinctive adsorption mechanisms.

scholarly journals Mechanisms and adsorption capacities of biochar for the removal of organic and inorganic pollutants from industrial wastewater

2020 ◽  
Author(s):  
T. G. Ambaye ◽  
M. Vaccari ◽  
E. D. van Hullebusch ◽  
A. Amrane ◽  
S. Rtimi
Keyword(s):  
Organic Contaminants ◽  
Pyrolysis Temperature ◽  
Low Cost ◽  
Industrial Effluents ◽  
Economic Benefits ◽  
Inorganic Pollutants ◽  
Solution Ph ◽  
Adsorption Mechanisms ◽  
Adsorption Capacities ◽  
Temperature Solution

AbstractCurrently, due to the rapid growth of urbanization and industrialization in developing countries, a large volume of wastewater is produced from industries that contain chemicals generating high environmental risks affecting human health and the economy if not treated properly. Consequently, the development of a sustainable low-cost wastewater treatment approach has attracted more attention of policymakers and scientists. The present review highlights the recent applications of biochar in removing organic and inorganic pollutants present in industrial effluents. The recent modes of preparation, physicochemical properties and adsorption mechanisms of biochar in removing organic and inorganic industrial pollutants are also reviewed comprehensively. Biochar showed high adsorption of industrial dyes up to 80%. It also discusses the recent application and mechanism of biochar-supported photocatalytic materials for the degradation of organic contaminants in wastewater. We reviewed also the possible optimizations (such as the pyrolysis temperature, solution pH) allowing the increase of the adsorption capabilities of biochar leading to organic contaminants removal. Besides, increasing the pyrolysis temperature of the biochar was seen to lead to an increase in its surface area, while it decreases their amount of oxygen-containing functional groups, consequently leading to a decrease in the adsorption of metal (loid) ions present in the medium. Finally, the review suggests that more research should be carried out to optimize the main parameters involved in biochar production and its regeneration methods. Future efforts should be also carried out towards process engineering to improve its adsorption capacity to increase the economic benefits of its implementation.

scholarly journals Husk of Agarwood Fruit-Based Hydrogel Beads for Adsorption of Cationic and Anionic Dyes in Aqueous Solutions

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1437
Author(s):  
Chih Ming Ma ◽  
Bo-Yuan Yang ◽  
Gui-Bing Hong
Keyword(s):  
Aqueous Solutions ◽  
Selective Adsorption ◽  
Order Model ◽  
Anionic Dyes ◽  
Adsorption Selectivity ◽  
Hydrogel Beads ◽  
Batch System ◽  
Initial Ph ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order

Hydrogel beads based on the husk of agarwood fruit (HAF)/sodium alginate (SA), and based on the HAF/chitosan (CS) were developed for the removal of the dyes, crystal violet (CV) and reactive blue 4 (RB4), in aqueous solutions, respectively. The effects of the initial pH (2–10) of the dye solution, the adsorbent dosage (0.5–3.5 g/L), and contact time (0–540 min) were investigated in a batch system. The dynamic adsorption behavior of CV and RB4 can be represented well by the pseudo-second-order model and pseudo-first-order model, respectively. In addition, the adsorption isotherm data can be explained by the Langmuir isotherm model. Both hydrogel beads have acceptable adsorption selectivity and reusability for the study of selective adsorption and regeneration. Based on the effectiveness, selectivity, and reusability of these hydrogel beads, they can be treated as potential adsorbents for the removal of dyes in aqueous solutions.

scholarly journals Driving forces of the diel distribution of phytoplankton functional groups in a shallow tropical lake (Lake Monte Alegre, Southeast Brazil)

2009 ◽  
Vol 69 (1) ◽  
pp. 75-85 ◽  
Author(s):  
LM. Rangel ◽  
LHS. Silva ◽  
MS. Arcifa ◽  
A. Perticarrari
Keyword(s):  
Vertical Distribution ◽  
Functional Groups ◽  
Rainy Season ◽  
Phytoplankton Biomass ◽  
Driving Forces ◽  
Circulation Pattern ◽  
Dry Period ◽  
Phytoplankton Functional Groups ◽  
The Vertical Distribution ◽  
Cool Dry Season

Phytoplankton vertical and diel dynamics in a small shallow lake (Lake Monte Alegre, Ribeirão Preto, state of São Paulo) were investigated in two climatological periods: July 2001 (cool-dry season) and March 2002 (warm-rainy season). Monte Alegre is a eutrophic reservoir, with a warm polymictic discontinuous circulation pattern. The lake was thermally stratified in both periods, although dissolved oxygen varied less in the cool-dry period. Phytoplankton biomass was higher in the warm-rainy season and the vertical distribution was stratified in both seasons. Flagellate groups (Lm, Y, W1 and W2) and functional groups typical of shallow eutrophic environments (J, X1 and Sn) were important throughout the study period. The lake's thermal pattern strongly influenced the vertical distribution of the phytoplankton community in both periods. Biomass, functional groups and size classes of phytoplankton also were determined by the presence of more efficient herbivores in the lake, especially during the cool-dry period when phytoplankton biomass decreased.

scholarly journals Palladium-Catalyzed [3+2] Cycloaddition via Two-Fold 1,3-C(sp3)−H Activation

2020 ◽  
Author(s):  
Hojoon Park ◽  
jin-quan yu
Keyword(s):  
Functional Groups ◽  
Sulfonic Acid ◽  
Cycloaddition Reaction ◽  
Wide Range ◽  
Leaving Group ◽  
Palladium Catalyzed ◽  
Directing Group ◽  
Overall Efficiency ◽  
Weak Coordination ◽  
Single Reaction

<div>Cycloaddition reactions provide an expeditious route to construct ring systems in a highly convergent and stereoselective manner. For a typical cycloaddition reaction to occur, however, the installation of multiple reactive functional groups (π-bonds, leaving group, etc.) are required within the substrates, compromising the overall efficiency or scope of the cycloaddition reaction. Here, we report a palladium-catalyzed [3+2] reaction that utilizes C(sp<sup>3</sup>)–H activation to generate the three-carbon unit for formal cycloaddition with maleimides. We implemented a strategy where the initial C(sp<sup>3</sup>)–H activation/olefin insertion would trigger a relayed, second remote C(sp<sup>3</sup>)–H activation to complete a formal [3+2] cycloaddition. The diastereoselectivity profile of this reaction resembles that of a typical pericyclic cycloaddition reaction in that the relationships between multiple stereocenters are exquisitely controlled in a single reaction. The key to success was the use of weakly coordinating amides as the directing group, as undesired Heck or alkylation pathways were preferred with other types of directing groups. The use of the pyridine-3-sulfonic acid ligands is critical to enable C(sp<sup>3</sup>)–H activation directed by this weak coordination. The method is compatible with a wide range of amide substrates, including lactams, which lead to novel spiro-bicyclic products. The [3+2] product is also shown to undergo a reductive desymmetrization process to access chiral cyclopentane bearing multiple stereocenters with excellent enantioselectivity.</div>

Selective adsorption mechanisms of pharmaceuticals on benzene-1,4-dicarboxylic acid-based MOFs: Effects of a flexible framework, adsorptive interactions and the DFT study

2020 ◽  
Vol 720 ◽  
pp. 137449 ◽  
Author(s):  
Dujduan Sompornpailin ◽  
Chalita Ratanatawanate ◽  
Chanchai Sattayanon ◽  
Supawadee Namuangruk ◽  
Patiparn Punyapalakul
Keyword(s):  
Dicarboxylic Acid ◽  
Selective Adsorption ◽  
Dft Study ◽  
Adsorption Mechanisms ◽  
Flexible Framework
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