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Cleaner Water Jun 2024Environmental sustainability has gained acceptance to achieving the goal of a secure ecosystem with a reliable management system. Heavy metal remediation of aqueous...
Environmental sustainability has gained acceptance to achieving the goal of a secure ecosystem with a reliable management system. Heavy metal remediation of aqueous streams is of special concern due to the intractability and persistence in the environment. Adsorption is a potential alternative to the existing inefficient conventional technologies for the removal and recovery of metal ions from aqueous solutions and becomes vital to align with the Sustainable Development Goals (SDGs) and mitigate the adverse environmental and social impacts. Calcium Alginate-Graphene oxide (CA-GO) composite has been synthesized for the adsorption of heavy metals including Cr, Cu, and Cd ions from tannery effluents. Graphene oxide is prepared from commercial graphite powder and reacted with sodium alginate and calcium chloride to form the beads of CA-GO composite. The developed composite was characterized by FTIR, elemental analysis, SEM, XRD analysis, and Raman spectroscopy. Moreover, the effect of pH, adsorbent dosage, contact time, and initial concentration of metal ions on the adsorption capacity were investigated through batch experiments. At a pH>3.0 (pHzpc), the carboxyl group of CA-GO was deprotonated to make the surface negatively charged and facilitate metal adsorption. The optimum pH and maximum adsorption capacity of CA-GO for removal of Cr(III), Cu(II), and Cd(II) were 4.5, 6.0, and 7.0, and 90.58, 108.57, and 134.77 mg g, respectively. The kinetics, adsorption isotherms, and thermodynamics were studied to determine the adsorption mechanism. The kinetic of adsorption adopted the second-order model. Thermodynamic parameter were calculated and the adsorption process was determined to be exothermic and spontaneous at room temperature. The developed composite has been efficaciously applied for the removal of metal ions and pollution from real tannery effluents.
PubMed: 38948691
DOI: 10.1016/j.clwat.2024.100016 -
Mycobiology 2024Eritadenine from shiitake mushroom is a secondary metabolite with hypocholesterolemic, hypotensive and antiparasitic properties, thus promising for pharmaceutical and...
Enhancing Eritadenine Production in Submerged Cultures of Shiitake ( Berk. Pegler) Using Blue LED Light and Activated Charcoal. Revealing Eritadenine's Novel In Vitro Bioherbicidal Activity Against .
Eritadenine from shiitake mushroom is a secondary metabolite with hypocholesterolemic, hypotensive and antiparasitic properties, thus promising for pharmaceutical and agricultural applications. Eritadenine is obtained from submerged mycelial cultures of shiitake, but the actual yields remain unsatisfactory to explore potential applications or industrial-scale production. In this study, green and blue LED lights were tested to increase yields of eritadenine in submerged cultures of shiitake. Notably, blue LEDs increased yields by 13-14 times, reaching 165.7 mg/L, compared to darkness (11.2 mg/L) and green light (12.1 mg/L) ( < 0.05, Tukey test). Nitrogen sources yeast extract (YE) and peptone (at 2 g/L) increased eritadenine production. YE promoted 22.6 mg/L, while peptone 18.3 mg/L. The recovery of eritadenine was evaluated using amberlite and activated charcoal (AC) adsorption isotherms. AC demonstrated the highest adsorption rate, with 75 mg of eritadenine per gram of AC, according to the Freundlich isotherm. The desorption rate reached 93.95% at pH 10. The extract obtained from submerged cultures had eritadenine content of 63.31%, corresponding to 87.86% of recovery, according to HPLC analysis. Furthermore, the novel bioherbicidal potential of eritadenine was tested on plants. The cultures extract containing eritadenine had a detrimental impact on plant development, generating mortality of 100% at 3%, 0.5%, and 0.25%. Moreover, pure eritadenine exhibited a phytotoxic effect similar than glyphosate on leaves, stems and roots. These findings highlight the significant bioherbicidal properties of eritadenine. Further studies are needed to understand the biosynthetic pathway of eritadenine and its bioherbicidal properties on weeds and illicit crops.
PubMed: 38948450
DOI: 10.1080/12298093.2024.2350207 -
APL Bioengineering Jun 2024Monoclonal antibodies (mAbs) can undergo structural changes due to interaction with oil-water interfaces during storage. Such changes can lead to aggregation, resulting...
Monoclonal antibodies (mAbs) can undergo structural changes due to interaction with oil-water interfaces during storage. Such changes can lead to aggregation, resulting in a loss of therapeutic efficacy. Therefore, understanding the microscopic mechanism controlling mAb adsorption is crucial to developing strategies that can minimize the impact of interfaces on the therapeutic properties of mAbs. In this study, we used MARTINI coarse-grained molecular dynamics simulations to investigate the adsorption of the Fab and Fc domains of the monoclonal antibody COE3 at the oil-water interface. Our aim was to determine the regions on the protein surface that drive mAb adsorption. We also investigate the role of protein concentration on protein orientation and protrusion to the oil phase. While our structural analyses compare favorably with recent neutron reflectivity measurements, we observe some differences. Unlike the monolayer at the interface predicted by neutron reflectivity experiments, our simulations indicate the presence of a secondary diffused layer near the interface. We also find that under certain conditions, protein-oil interaction can lead to a considerable distortion in the protein structure, resulting in enhanced adsorption behavior.
PubMed: 38948350
DOI: 10.1063/5.0207959 -
Frontiers in Chemistry 2024The deterioration of mild steel in an acidic environment poses a significant challenge in various industries. The emergence of effective corrosion inhibitors has drawn...
Unraveling the corrosion inhibition behavior of prinivil drug on mild steel in 1M HCl corrosive solution: insights from density functional theory, molecular dynamics, and experimental approaches.
The deterioration of mild steel in an acidic environment poses a significant challenge in various industries. The emergence of effective corrosion inhibitors has drawn attention to studies aimed at reducing the harmful consequences of corrosion. In this study, the corrosion inhibition efficiency of Prinivil in a 1M HCl solution through various electrochemical and gravimetric techniques has been investigated for the first time. The results demonstrated that the inhibition efficiency of Prinivil expanded from 61.37% at 50 ppm to 97.35% at 500 ppm concentration at 298 K. With a regression coefficient ( ) of 0.987, K value of 0.935 and E value of 43.024 kJ/mol at 500 ppm concentration of inhibitor, a strong affinity of Prinivil for adsorption onto the metal surface has been significantly found. Scanning electron microscopy (SEM) and contact angle measurement analyses further support the inhibitory behavior of Prinivil, demonstrating the production of a defensive layer on the surface of mild steel. Additionally, molecular dynamics (MD) and Monte Carlo simulations were employed to investigate the stability and interactions between Prinivil and the metallic surface (Fe (1 1 0)) at the atomic level. The computed results reveal strong adsorption of Prinivil upon the steel surface, confirming its viability as a corrosion inhibitor.
PubMed: 38947959
DOI: 10.3389/fchem.2024.1403118 -
Frontiers in Chemistry 20245-Hydroxymethylfurfural (HMF), serving as a versatile platform compound bridging biomass resource and the fine chemicals industry, holds significant importance in... (Review)
Review
5-Hydroxymethylfurfural (HMF), serving as a versatile platform compound bridging biomass resource and the fine chemicals industry, holds significant importance in biomass conversion processes. The electrooxidation of HMF plays a crucial role in yielding the valuable product (2,5-furandicarboxylic acid), which finds important applications in antimicrobial agents, pharmaceutical intermediates, polyester synthesis, and so on. Defect engineering stands as one of the most effective strategies for precisely synthesizing electrocatalytic materials, which could tune the electronic structure and coordination environment, and further altering the adsorption energy of HMF intermediate species, consequently increasing the kinetics of HMF electrooxidation. Thereinto, the most routine and effective defect are the anionic vacancies and cationic vacancies. In this concise review, the catalytic reaction mechanism for selective HMF oxidation is first elucidated, with a focus on the synthesis strategies involving both anionic and cationic vacancies. Recent advancements in various catalytic oxidation systems for HMF are summarized and synthesized from this perspective. Finally, the future research prospects for selective HMF oxidation are discussed.
PubMed: 38947956
DOI: 10.3389/fchem.2024.1416329 -
Frontiers in Plant Science 2024Phosphorus (P) availability severely limits plant growth due to its immobility and inaccessibility in soils. Yet, visualization and measurements of P uptake from...
Phosphorus (P) availability severely limits plant growth due to its immobility and inaccessibility in soils. Yet, visualization and measurements of P uptake from different root types or regions in soil are methodologically challenging. Here, we explored the potential of phosphor imaging combined with local injection of radioactive P to quantitatively visualize P uptake and translocation along roots of maize grown in soils. Rhizoboxes (20 × 40 × 1 cm) were filled with sandy field soil or quartz sand, with one maize plant per box. Soil compartments were created using a gravel layer to restrict P transfer. After 2 weeks, a compartment with the tip region of a seminal root was labeled with a NaH PO4 solution containing 12 MBq of P. Phosphor imaging captured root P distribution at 45 min, 90 min, 135 min, 180 min, and 24 h post-labeling. After harvest, P levels in roots and shoots were quantified. P uptake exhibited a 50% increase in quartz sand compared to sandy soil, likely attributed to higher P adsorption to the sandy soil matrix than to quartz sand. Notably, only 60% of the absorbed P was translocated to the shoot, with the remaining 40% directed to growing root tips of lateral or seminal roots. Phosphor imaging unveiled a continuous rise in P signal in the labeled seminal root from immediate post-labeling until 24 h after labeling. The highest P activities were concentrated just above the labeled compartment, diminishing in locations farther away. Emerging laterals from the labeled root served as strong sinks for P, while a portion was also transported to other seminal roots. Our study quantitatively visualized P uptake and translocation dynamics, facilitating future investigations into diverse root regions/types and varying plant growth conditions. This improves our understanding of the significance of different P sources for plant nutrition and potentially enhances models of plant P uptake.
PubMed: 38947946
DOI: 10.3389/fpls.2024.1376613 -
Sustainable Chemistry For the... Jun 2024Untreated tannery wastewater contains a large amount of toxic metals, dyes, and other pollutants, which pose adverse effects on the ecosystem and public health. In this...
Untreated tannery wastewater contains a large amount of toxic metals, dyes, and other pollutants, which pose adverse effects on the ecosystem and public health. In this work, a calcium alginate-poly vinyl alcohol-graphene oxide (CA-PVA-GO) composite was prepared to remove metals and dyes, particularly Cr(Ⅲ) and CI acid violet 54 (AV54) dye, from tannery wastewater. FESEM, FTIR, and XRD analyses were applied to characterize the GO and CA-PVA-GO. Different operational variables, viz. pH (3.0-5.5 for Cr(III) and 2-7 for dye), dosage (0.164-2.46 g/L), contact time (10-60 min), initial concentration (39, 65, 98, and 201 ppm for Cr(III) and 21.5, 38.5, 54.5, and 61.75 ppm for dye), and temperature (298, 308, 318, and 328 K) were studied to evaluate the efficiency of the CA-PVA-GO composite. The optimum conditions for Cr(Ⅲ) and AV54 dye adsorption were found to be pH (5.0 and 3.0), dosage (0.82 g/L for both), and time (45 and 60 min), respectively, with 35.35 ± 1.43% and 84.63 ± 2.54% removal efficiency. The experimental data was analyzed through the Langmuir and Freundlich isotherms. The maximum adsorption capacity (q) was observed at 173.01 and 74.68 mg/g for Cr(Ⅲ) and AV54 dye, respectively. The pseudo-second-order kinetic model was fitted better (R = 0.981, 0.995, 0.92, and 0.995) than first-order for AV54 dye adsorption. Thermodynamic analyses revealed that the Cr(Ⅲ) and AV54 dye adsorption processes were spontaneous and exothermic. The value of Gibbs free energy (ΔG) for Cr(III) adsorption was obtained at -7.433, -4.508, -2.626, and -1.311 kJ/mol, whereas it was -5.178, -4.867, -4.628, and -4.555 kJ/mol for dye. The values of ΔH and ΔS were -67.257 and -0.198 kJ/mol for Cr(III) and -10.852 and -0.019 kJ/mol for the dye removal. The regenerated CA-PVA-GO composite was reused successfully. Different physicochemical parameters, viz., concentration, pH, TDS, EC, BOD, and COD of chrome tanning and dyeing effluents, were analyzed before and after the adsorption. The results of chromium and dye removal from tannery wastewater were 53.18% and 93.91%, revealing that the developed eco-friendly CA-PVA-GO composite could be an operative adsorbent for tannery wastewater treatment and possibly scaled up to an industrial level.
PubMed: 38947873
DOI: 10.1016/j.scenv.2024.100092 -
ACS Omega Jun 2024Electrospinning technology for fabricating nanofiber films and the Hummer method for synthesizing graphene oxide (GO), along with subsequent reduction, have been...
Electrospinning technology for fabricating nanofiber films and the Hummer method for synthesizing graphene oxide (GO), along with subsequent reduction, have been significantly advanced, demonstrating immense potential for large-scale industrial applications. Nanofibrous films loaded with reduced graphene oxide (rGO) have been widely explored for their applications in electromagnetic shielding, the biomedical fields, and pollutant adsorption. However, fragile mechanical performance of electrospun fibers with limited surface post-treatment methods has somewhat hindered their further industrial development. In response to this challenge, we propose a dual-regulation strategy involving post-treatment to form porous nanofiber films and the controlled flake size of rGO for surface coating during preparation. This approach aims to achieve poly(l-lactic acid) (PLLA)/rGO electrospun fibrous films with enhanced mechanical properties. It offers a roadmap for the continued application and standardized production of fibrous films loaded with rGO.
PubMed: 38947839
DOI: 10.1021/acsomega.4c01976 -
ACS Omega Jun 2024We explore the photodetection properties of a carbon nanofiber (CNF)-based p-CNF/n-Si heterojunction device in the 400-800 nm wavelength range and investigate the...
We explore the photodetection properties of a carbon nanofiber (CNF)-based p-CNF/n-Si heterojunction device in the 400-800 nm wavelength range and investigate the changes brought in by adsorption of CuNi (CN) nanoparticles on the CNFs. The nanoparticles and CN-CNF nanocomposites were synthesized by using chemical hydrothermal routes. The p-type semiconducting nature of the CNFs and nanocomposites was determined using X-ray photoelectron (XPS) and UV-vis spectroscopies. The p-CNF/n-Si device is found to be better than many carbon-nanotube-based devices in terms of its peak responsivity (0.6 A/W) and gain (1.6), with an acceptably moderate peak detectivity (1.3 × 10 Jones) at 450 nm and a -5 V bias. The p-CN-CNF/n-Si device displays an appreciable enhancement in the photoresponse with respect to the p-CNF/n-Si device, with a peak responsivity of 2.8 A/W, peak detectivity of 9.4 × 10 Jones, and gain of 8. With the aid of valence band XPS and Raman spectra, the enhancement is explainable in terms of a CN to CNF charge transfer and the resulting increase in the built-in potential at the heterojunction.
PubMed: 38947801
DOI: 10.1021/acsomega.4c01546 -
ACS Omega Jun 2024Oligocene-Pliocene shale reservoirs in the Western Qaidam Depression represent typical mixed shale deposits characterized by moderate organic matter (OM) abundance and...
Oligocene-Pliocene shale reservoirs in the Western Qaidam Depression represent typical mixed shale deposits characterized by moderate organic matter (OM) abundance and sufficient OM maturity, indicating substantial shale-oil resource potential. Here, a comprehensive study was conducted to analyze the reservoir characteristics of different shale types, including the Upper Xiaganchaigou (late Oligocene), Shangganchaigou (Miocene), and Xiayoushashan (early Pliocene) Formations in the Western Qaidam Depression. Our analysis focused on the pore structural characteristics of shale reservoirs, employing X-ray diffraction, casting thin sections, scanning electron microscopy, low-temperature nitrogen adsorption, and nuclear magnetic resonance (NMR) as investigative techniques. Our results show that (1) the study area comprises five typical shale types: lime shale, argillaceous shale, limestone, argillaceous limestone, and mudstone. The best hydrocarbon source rock conditions are found in the lime shale and argillaceous shale. (2) Inorganic pores, including dissolution pores, intergranular pores, bedding fractures, structural fractures, and intraparticle pores in clay minerals, are the main pore types found in the studied samples and constitute the primary reservoir space for shale oil. On the basis of fractal dimensions obtained through NMR, the pores can be classified as micropores (<100 nm), mesopores (100-1000 nm), or macropores (>1000 nm). Mesopores are the main contributors to porosity. (3) The development of micropores is positively correlated with clay mineral content. The development of mesopores and macropores is influenced by the quartz, feldspar, dolomite, and calcite contents. Calcite content exhibits a negative correlation with porosity, suggesting that later-stage pore cementation hinders shale reservoir development. (4) The five typical shale reservoirs in the study area can be categorized into three types. Type I reservoir lithologies include lime shale and argillaceous shale; type II reservoir lithologies include limestone and argillaceous limestone; and type III reservoirs comprise mudstone. Type I and II reservoirs are of better quality than type III.
PubMed: 38947797
DOI: 10.1021/acsomega.4c03956