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International Journal of Molecular... Mar 2023The application of the adsorption method in sewage treatment has recently become a hot spot. A novel magnetic clay-biochar composite (BNT-MBC) was fabricated by...
The application of the adsorption method in sewage treatment has recently become a hot spot. A novel magnetic clay-biochar composite (BNT-MBC) was fabricated by co-pyrolysis of bentonite and biomass after being impregnated with Fe (NO)·9HO. Its adsorption capacity for Cd(II) and methyl orange was approximately doubled, reaching a maximum of 26.22 and 63.34 mg/g, and could be easily separated from the solution by using external magnets with its saturation magnetization of 9.71 emu/g. A series of characterizations including surface morphology and pore structure, elemental analysis, functional group analysis and graphitization were carried out, showing that the specific surface area was increased 50 times by loading 20 wt.% bentonite, while its graphitization and oxygen-containing functional groups were also enhanced. The isotherm fitting indicated that Cd(II) was adsorbed in multiple layers, while methyl orange was in both monolayer and multilayer adsorptions. The kinetic fitting indicated that chemisorption was the rate-limiting step of both, and it was also a complex process controlled by two steps with the fitting of intra-particle diffusion. In the binary system of Cd(II) and methyl orange, the co-existing pollutants facilitated the adsorption of the original one, and there was no competition between adsorption sites of Cd(II) and methyl orange. BNT-MBC also exhibited good reusability and can be magnetically recovered for recycling. Thus, the magnetic clay-biochar composite BNT-MBC is a cost-effective and promising adsorbent for simultaneous removing Cd(II) and methyl orange from wastewater.
Topics: Adsorption; Cadmium; Clay; Bentonite; Charcoal; Water; Magnetic Phenomena; Water Pollutants, Chemical; Kinetics
PubMed: 36982828
DOI: 10.3390/ijms24065755 -
International Journal of Environmental... Dec 2022In our work, the transition-metal-oxide precursor (TMO@BC, M = Fe, Co, Ni) has been loaded on the pollen carbon by the hydrothermal method and annealed at different...
In our work, the transition-metal-oxide precursor (TMO@BC, M = Fe, Co, Ni) has been loaded on the pollen carbon by the hydrothermal method and annealed at different temperatures to generate a composite material of metal oxide and pollen carbon in this study, which can effectively prevent agglomeration caused by a small size and magnetism. The XRD patterns of the samples showed that the as-synthesized metal oxides were γ-FeO, CoO, and NiO. In the 20 mg/L methyl orange adsorption experiment, the adsorption amount of CoO@C at 500 ℃ reached 19.32 mg/g and the removal rate was 96.61%. Therefore, CoO@C was selected for the adsorption correlation-model-fitting analysis, which was in line with the secondary reaction. The pseudo-second-order kinetic model (: 0.9683-0.9964), the intraparticle diffusion model, and the Freundlich adsorption isotherm model indicated that the adsorption process was the result of both physical and chemical adsorptions, and the judgment was based on the electrostatic action. The adsorption and removal efficiency of ciprofloxacin (CIP) by changing the pH of the reaction was about 80%, so the electrostatic attraction worked, but not the main factor. Recovered by an external magnetic field, the three-time recycling efficiency was still maintained at more than 80%. This novel biomass-derived magnetic porous carbon material embedded with transition-metal-oxide nanoparticles is highly promising for many applications, especially in the field of environmental remediation.
Topics: Oxides; Carbon; Porosity; Metals; Adsorption; Metal Nanoparticles; Magnetic Phenomena; Water Pollutants, Chemical; Kinetics; Charcoal
PubMed: 36554621
DOI: 10.3390/ijerph192416740 -
Colloids and Surfaces. B, Biointerfaces Sep 2022This work presents a study of the lysozyme release from crosslinked TEMPO nanocellulose (TOCNF) and alginate (ALG) hydrogels in a medium with different ionic strength...
This work presents a study of the lysozyme release from crosslinked TEMPO nanocellulose (TOCNF) and alginate (ALG) hydrogels in a medium with different ionic strength and temperature. The main objective is to develop a mathematical model for a detailed study of the concurrent action of diffusion mechanism and adsorption/desorption kinetics. Model fit parameters provide important information about the initial (maximum) adsorption rate and its deceleration with increasing ionic strength of the release medium. Similarly, the initial (minimum) desorption rate and its acceleration with increasing salt concentration can be determined. The model leads us to the conclusion that the initial adsorption rate is higher in the case of TOCNF, but due to fewer electrostatic interactions and morphology as well as topography of the surface, it decreases to a negligible value much faster than in the case of ALG, where the diffusion process becomes dominant.
Topics: Adsorption; Alginates; Diffusion; Hydrogels; Hydrogen-Ion Concentration; Kinetics; Proteins
PubMed: 35792530
DOI: 10.1016/j.colsurfb.2022.112677 -
Analytical Sciences : the International... 2021A nanoporous material has been applied for the development of functional nanobiomaterials by utilizing its uniform pore structure and large adsorption capacity. The... (Review)
Review
A nanoporous material has been applied for the development of functional nanobiomaterials by utilizing its uniform pore structure and large adsorption capacity. The structure and stability of biomacromolecules, such as peptide, oligonucleotide, and protein, are primary factors to govern the performance of nanobiomaterials, so that their direct characterization methodologies are in progress. In this review, we focus on recent topics in the structural characterization of protein molecules adsorbed at a nanoporous material with uniform meso-sized pores. The thermal stabilities of the adsorbed proteins are also summarized to discuss whether the structure of the adsorbed protein molecules can be stabilized or not.
Topics: Adsorption; Nanopores; Proteins; Surface Properties
PubMed: 33431779
DOI: 10.2116/analsci.20SAR05 -
Anais Da Academia Brasileira de Ciencias 2023Despite being little explored for petroporphyrins recovery from oils and bituminous shales, adsorption and desorption processes can be feasible alternatives to obtain a...
Despite being little explored for petroporphyrins recovery from oils and bituminous shales, adsorption and desorption processes can be feasible alternatives to obtain a similar synthetic material, and to characterize their original organic materials. Experimental designs were used to analyze the effects of qualitative (e.g., type of adsorbent, solvent, and diluent) and quantitative (e.g., temperature and solid/liquid ratio) variables on the adsorptive and desorptive performance regarding nickel octaethylporphyrin (Ni-OEP) removal using carbon-based adsorbents. The evaluation variables, adsorption capacity (qe ) and desorption percentage (%desorption ) were optimized by means of the Differential Evolution algorithm. The most efficient adsorbent for removing/recovery Ni-OEP was activated-carbon coconut shell, in which dispersive π-π type and acid-base interactions were likely formed. The highest values of qe and %desorption were obtained using toluene as solvent, chloroform as diluent, 293 K as temperature, and 0.5 mg.mL-1 as solid/liquid ratio for adsorption, and a higher temperature (323 K) and lower solid/liquid ratio (0.2 mg.mL-1) for desorption. The optimization process resulted in qe of 6.91 mg.g-1 and %desorption of 35.2%. In the adsorption-desorption cycles, approximately 77% of the adsorbed porphyrins were recovered. The results demonstrated the potential of carbon-based materials as adsorbent materials for obtaining porphyrin compounds from oils and bituminous shales.
Topics: Nickel; Carbon; Adsorption; Porphyrins; Excipients; Solvents
PubMed: 37341271
DOI: 10.1590/0001-3765202320211598 -
Molecules (Basel, Switzerland) Dec 2022Recent studies on the removal of pollutants via adsorption include the use of carbon-based adsorbents, due to their high porosity and large surface area; however, such...
Recent studies on the removal of pollutants via adsorption include the use of carbon-based adsorbents, due to their high porosity and large surface area; however, such materials lack photoactive properties. This study evaluates the synergistic effect of integrated mesoporous carbon xerogel (derived from resorcinol formaldehyde) and titanium dioxide (TiO) for combined adsorption and photodegradation application. The complex formed between carbon xerogel and TiO phase was investigated through FTIR, proving the presence of a Ti-O-C chemical linkage. The physicochemical properties of the synthesised adsorbent-photocatalyst were probed using FESEM, BET analysis and UV-Vis analysis. The kinetics, equilibrium adsorption, effect of pH, and effect of adsorbent dosage were investigated. The expansion of the absorbance range to the visible range was verified, and the corresponding band gap evaluated. These properties enabled a visible light response when the system was exposed to visible light post adsorption. Hence, an assistive adsorption-photodegradation phenomenon was successfully executed. The adsorption performance exhibited 85% dye degradation which improved to 99% following photodegradation. Further experiments showed the reduction of microorganisms under visible light, where no microbial colonies were observed after treatment, indicating the potential application of these composite materials.
Topics: Environmental Pollutants; Photolysis; Titanium; Adsorption; Carbon; Catalysis
PubMed: 36500576
DOI: 10.3390/molecules27238483 -
Journal of Pharmaceutical Sciences Nov 2021Protein aggregate formation in prefilled syringes (PFSs) can be influenced by protein adsorption and desorption at the solid-liquid interface. Although inhibition of...
Protein aggregate formation in prefilled syringes (PFSs) can be influenced by protein adsorption and desorption at the solid-liquid interface. Although inhibition of protein adsorption on the PFS surface can lead to a decrease in the amount of aggregation, the mechanism underlying protein adsorption-mediated aggregation in PFSs is unclear. This study investigated protein aggregation caused by protein adsorption on silicone oil-free PFS surfaces [borosilicate glass (GLS) and cycloolefin polymer (COP)] and the factors affecting the protein adsorption on the PFS surfaces. The adsorbed proteins formed multilayered structures that consisted of two distinct types of layers: proteins adsorbed on the surface of the material and proteins adsorbed on top of the proteins on the surface. A pH-dependent electrostatic interaction was the dominant force for protein adsorption on the GLS surface, while hydrophobic effects were dominant for protein adsorption on the COP surface. When the repulsion force between proteins was weak, protein adsorption on the adsorbed protein layer was increased for both materials and as a result, protein aggregation increased. Therefore, a formulation with high colloidal stability can minimize protein adsorption on the COP surface, leading to reduced protein aggregation.
Topics: Adsorption; Hydrophobic and Hydrophilic Interactions; Proteins; Silicone Oils; Surface Properties; Syringes
PubMed: 34310973
DOI: 10.1016/j.xphs.2021.07.007 -
ChemMedChem May 2022In silico adsorption of eight antimalarials that inhibit β-hematin (synthetic hemozoin) formation identified a primary binding site on the (001) face, which...
In silico adsorption of eight antimalarials that inhibit β-hematin (synthetic hemozoin) formation identified a primary binding site on the (001) face, which accommodates inhibitors via formation of predominantly π-π interactions. A good correlation (r =0.64, P=0.017) between adsorption energies and the logarithm of β-hematin inhibitory activity was found for this face. Of 53 monocyclic, bicyclic and tricyclic scaffolds, the latter yielded the most favorable adsorption energies. Five new amino-phenoxazine compounds were pursued as β-hematin inhibitors based on adsorption behaviour. The 2-substituted phenoxazines show good to moderate β-hematin inhibitory activity (<100 μM) and Plasmodium falciparum blood stage activity against the 3D7 strain. N ,N -diethyl-N -(10H-phenoxazin-2-yl)pentane-1,4-diamine (P2a) is the most promising hit with IC values of 4.7±0.6 and 0.64±0.05 μM, respectively. Adsorption energies are predictive of β-hematin inhibitory activity, and thus the in silico approach is a beneficial tool for structure-based development of new non-quinoline inhibitors.
Topics: Adsorption; Antimalarials; Hemeproteins; Plasmodium falciparum
PubMed: 35385211
DOI: 10.1002/cmdc.202200139 -
Marine Drugs Mar 2022Emodin, a hydroxyanthraquinone derivative, has been used as medicine for more than 2000 years due to its extensive pharmacological activities. Large-scale production of...
Emodin, a hydroxyanthraquinone derivative, has been used as medicine for more than 2000 years due to its extensive pharmacological activities. Large-scale production of emodin has been achieved by optimizing the fermentation conditions of marine-derived HN4-13 in a previous study. However, the fermentation broth contained complex unknown components, which adversely affected the study of emodin. Herein, the conditions for the enrichment of emodin from . HN4-13 extract using XAD-16 resin were optimized, and a separation method with high efficiency, simple operation, a low cost, and a large preparative scale was established. The adsorption process of emodin on the XAD-16 resin conformed to pseudo-second-order kinetics and Langmuir models. The optimal conditions for the adsorption process were as follows: An emodin concentration, flow rate, and loading volume of 0.112 mg/mL, 2 BV/h, and 10 BV, respectively. For desorption, 50% ethanol was used to elute impurities and 80% ethanol was used to desorb emodin. After enrichment with XAD-16 resin, the emodin content increased from 1.16% to 11.48%, and the recovery rate was 75.53% after one-step treatment. These results demonstrate the efficiency of the simple adsorption-desorption strategy, using the XAD-16 resin for emodin enrichment.
Topics: Adsorption; Aspergillus; Emodin; Ethanol; Plant Extracts
PubMed: 35447904
DOI: 10.3390/md20040231 -
Scientific Reports Oct 2022Improving boiling is challenging due to the unpredictable nature of bubbles. One way to enhance boiling is with surfactants, which alter the solid-liquid and...
Improving boiling is challenging due to the unpredictable nature of bubbles. One way to enhance boiling is with surfactants, which alter the solid-liquid and liquid-vapor interfaces. The conventional wisdom established by previous studies suggests that heat transfer enhancement is optimized near the critical micelle concentration (CMC), which is an equilibrium property that depends on surfactant type. However, these studies only tested a limited number of surfactants over small concentration ranges. Here, we test a larger variety of nonionic and anionic surfactants over the widest concentration range and find that a universal, optimal concentration range exists, irrespective of CMC. To explain this, we show that surfactant-enhanced boiling is controlled by two competing phenomena: (1) the dynamic adsorption of surfactants to the interfaces and (2) the increase in liquid dynamic viscosity at very high surfactant concentrations. This dynamic adsorption is time-limited by the millisecond-lifetime of bubbles on the boiling surface-much shorter than the timescales required to see equilibrium behaviors such as CMC. At very high concentrations, increased viscosity inhibits rapid bubble growth, reducing heat transfer. We combine the effects of adsorption and viscosity through a simple proportionality, providing a succinct and useful understanding of this enhancement behavior for boiling applications.
Topics: Surface-Active Agents; Adsorption; Micelles; Pulmonary Surfactants; Excipients
PubMed: 36307430
DOI: 10.1038/s41598-022-21313-1