| 11. |
- Antonio, Capezza, et al.
(författare)
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Preparation and Comparison of Reduced Graphene Oxide and Carbon Nanotubes as Fillers in Conductive Natural Rubber for Flexible Electronics
- 2019
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Ingår i: Omega. - : American Chemical Society (ACS). - 0030-2228 .- 1541-3764. ; 4:2
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Tidskriftsartikel (refereegranskat)abstract
- Conductive natural rubber (NR) nanocomposites were prepared by solvent-casting suspensions of reduced graphene oxide(rGO) or carbon nanotubes (CNTs), followed by vulcanization of the rubber composites. Both rGO and CNT were compatible as fillers in the NR as well as having sufficient intrinsic electrical conductivity for functional applications. Physical (thermal) and chemical reduction of GO were investigated, and the results of the reductions were monitored by X-ray photoelectron spectroscopy for establishing a reduction protocol that was useful for the rGO nanocomposite preparation. Field-emission scanning electron microscopy showed that both nanofillers were adequately dispersed in the main NR phase. The CNT composite displays a marked mechanical hysteresis and higher elongation at break, in comparison to the rGO composites for an equal fraction of the carbon phase. Moreover, the composite conductivity was always ca. 3-4 orders of magnitude higher for the CNT composite than for the rGO composites, the former reaching a maximum conductivity of ca. 10.5 S/m, which was explained by the more favorable geometry of the CNT versus the rGO sheets. For low current density applications though, both composites achieved the necessary percolation and showed the electrical conductivity needed for being applied as flexible conductors for a light-emitting diode.
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| 12. |
- Anusuyadevi, Prasaanth Ravi, et al.
(författare)
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Floating Photocatalysts for Effluent Refinement Based on Stable Pickering Cellulose Foams and Graphitic Carbon Nitride (g-C3N4)
- 2020
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 5:35, s. 22411-22419
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Tidskriftsartikel (refereegranskat)abstract
- The transfer of heterogeneous photocatalysis applications from the laboratory to real-life aqueous systems is challenging due to the higher density of photocatalysts compared to water, light attenuation effects in water, complicated recovery protocols, and metal pollution from metal-based photocatalysts. In this work, we overcome these obstacles by developing a buoyant Pickering photocatalyst carrier based on green cellulose nanofibers (CNFs) derived from wood. The air bubbles in the carrier were stable because the particle surfactants provided thermodynamic stability and the derived photocatalytic foams floated on water throughout the test period (4 weeks). A metal-free semiconductor photocatalyst, g-C3N4, was facilely embedded inside the foam by mixing the photocatalyst with the air-bubble suspension followed by casting and drying to produce solid foams. When tested under mild irradiation conditions (visible light, low energy LEDs) and no agitation, almost three times more dye was removed after 6 h for the floating g-C3N4-CNF nanocomposite foam, compared to the pure g-C3N4 powder residing on the bottom of a ca. 2 cm-high water pillar. The buoyancy and physicochemical properties of the carrier material were imperative to render escalated oxygenation, high photon utilization, and faster dye degradation. The reported assembly protocol is facile, general, and provides a new strategy for assembling green floating foams that can potentially carry a number of different photocatalysts.
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| 13. |
- Aouelela, Marwa H. A., et al.
(författare)
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Synthesis and Characterization of Molybdenum- and Sulfur-Doped FeSe
- 2023
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 8:39, s. 36553-36561
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Tidskriftsartikel (refereegranskat)abstract
- During the past decade, two-dimensional (2D) layered materials opened novel opportunities for the exploration of exciting new physics and devices owing to their physical and electronic properties. Among 2D materials, iron selenide has attracted much attention from several physicists as they provide a fruitful stage for developing new superconductors. Chemical doping offers a powerful approach to manipulate and optimize the electronic structure and physical properties of materials. Here, to reveal how doping affects the physical properties in FeSe, we report on complementary measurements of molybdenum- and sulfur-doped FeSe with theoretical calculations. Mo0.1Fe0.9Se0.9S0.1 was synthesized by a one-step solid-state reaction method. Crystal structure and morphology were studied using powder X-ray diffraction and scanning electron microscopy. Thermal stability and decomposition behavior in doped samples were studied by thermogravimetric analysis, and to understand the microscopic influence of doping, we performed Raman spectroscopy. First-principles calculations of the electronic structure illustrate distinct changes of electronic structures of the substituted FeSe systems, which can be responsible for their superconducting properties.
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| 14. |
- Arkell, Karolina, et al.
(författare)
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Mechanistic Modeling of Reversed-Phase Chromatography of Insulins with Potassium Chloride and Ethanol as Mobile-Phase Modulators
- 2017
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 2, s. 136-146
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Tidskriftsartikel (refereegranskat)abstract
- The purpose of this study was to investigate the adsorption mechanism in reversed-phase chromatography (RPC) of proteins and to develop a model for the effect of dual mobile phase modulators—a salt and an organic solvent—on this process. Two different adsorption mechanisms were considered: (1) pure association of a protein molecule and one or more ligands and (2) displacement of the organic modulator, with which the adsorbent is saturated, by the protein upon association with one or more ligands. One model was then derived from each of the two considered mechanisms, combining thermodynamic theories on salting-in, RPC, and the solubility of proteins. The model was then applied to chromatographic data from an earlier report as well as supplementary data for solubility and vapor–liquid equilibria, and case-specific simplifications were made. We found that an adaptation of Kirkwood’s electrostatic theories to hydrophobic interaction chromatography describes the observed effect of KCl well. Combining chromatographic and solubility data for one of the insulins, we concluded that the variation in the activity coefficient of the insulin with respect to the concentration of ethanol alone cannot describe its effect on retention. Consequently, one or more other phenomena must affect the adsorption process. Our second model fits the retention data well, supporting the hypothesis that ethanol is directly involved in the adsorption mechanism in this case. Using additional experiments at a high-protein load, we extended the linear-range equilibrium model into a dynamic model for preparative conditions. This model shows good agreement with the high-load data for one of the insulin variants, without any additional effects of the modulator concentrations on the adsorption capacity.
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| 15. |
- Arkell, Karolina, et al.
(författare)
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Mechanistic Modeling of Reversed-Phase Chromatography of Insulins within the Temperature Range 10–40 °C
- 2018
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 3:2, s. 1946-1954
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Tidskriftsartikel (refereegranskat)abstract
- In the many published theories on the retention in reversed-phase chromatography (RPC), the focus is generally on the effect of the concentration of the mobile phase modulator(s), although temperature is known to have a significant influence both on the retention and on the selectivity between the adsorbates. The aim of this study was to investigate and model the combined effects of the temperature and the modulator concentrations on RPC of three insulin variants. KCl and ethanol were used as mobile phase modulators, and the experiments were performed on two different adsorbents, with C18 and C4 ligands. The temperature dependence was investigated for the interval 10–40 °C and at two different concentrations of each modulator. The model is derived from the expression for the adsorption equilibrium, which assumes that ethanol is adsorbed to the ligands and displaced by the insulin molecules, similar to the displacement of counterions in the steric mass-action model for ion-exchange chromatography. A good model fit to the new linear-range retention data was achieved by only adding and calibrating three parameters for the temperature dependence of the equilibrium. We found that a lower temperature results in a longer retention time for all adsorbates, adsorbents, and modulator concentrations used in this study, indicating that the adsorption process is enthalpy-driven. A comparison of the different contributions to the temperature dependence revealed that the large contribution from the equilibrium constant is dampened by the significant contributions of the opposite sign from the changes in activity coefficients of insulins and ethanol. Neglect of these effects when comparing different adsorbents and modulators might yield incorrect conclusions because the equilibrium constant varies with both, whereas the activity coefficients should be independent of the adsorbent. As expected, the conditions that promote higher retention also give a higher selectivity between the adsorbates. Nonetheless, in relation to its effect on the retention, the influence of the KCl concentration on the selectivity was significantly stronger than that of the temperature or that of the ethanol concentration.
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| 16. |
- Arkhipov, Victor P., et al.
(författare)
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Micelles of Oxyethylated Isononylphenols in Aqueous Solutions and Hydrophilic–Lipophilic Balance
- 2020
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 5:43, s. 28224-28232
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Tidskriftsartikel (refereegranskat)abstract
- We have measured the self-diffusion coefficients and calculated the effective hydrodynamic radii of micelles of ethoxylated isononylphenols in aqueous solutions in the presence of sodium chloride, as well as in their binary mutual mixtures, when approaching cloudy conditions. These cloudy conditions were created by an increase in temperature, a change in the concentration of an electrolyte in the solution, or a mutual ratio of neonols in their binary mixtures. The results are discussed within the concept of the hydrophilic–lipophilic balance.
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| 17. |
- Arkhipov, Victor P., et al.
(författare)
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Rhamnolipid Biosurfactant: Use for the Removal of Phenol from Aqueous Solutions by Micellar Solubilization
- 2023
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Ingår i: ACS Omega. - : American Chemical Society. - 2470-1343. ; 8:33, s. 30646-30654
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Tidskriftsartikel (refereegranskat)abstract
- Selective measurements of the self-diffusion coefficients of molecules of the biological surfactant rhamnolipid (RL) in individual aqueous solutions and in solutions with phenol as a solubilizate were carried out by nuclear magnetic resonance (NMR) diffusometry. Based on the obtained results, the solubilization characteristics of RLs were calculated. They are the fraction of solubilized phenol molecules, the phenol micelle-water distribution coefficient, the molar solubilization coefficient, the hydrodynamic radii of RL monomers and micelles, the aggregation numbers of micelles, and the solubilization capacity of micelles. Fraction of the solubilized phenol molecules increases and approaches 80-90% with increasing RL concentration. The solubilization capacity of the micelles increases from several units to 102 with an increase in both the concentration of RLs and the concentration of phenol in solution.
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| 18. |
- Arora, Neha, et al.
(författare)
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NMR-Based Metabolomic Approach To Elucidate the Differential Cellular Responses during Mitigation of Arsenic(III, V) in a Green Microalga
- 2018
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 3:9, s. 11847-11856
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Tidskriftsartikel (refereegranskat)abstract
- Nuclear magnetic resonance (NMR)-based metabolomic approach is a high-throughput fingerprinting technique that allows a rapid snapshot of metabolites without any prior knowledge of the organism. To demonstrate the applicability of NMR-based metabolomics in the field of microalgal-based bioremediation, novel freshwater microalga Scenedesmus sp. IITRIND2 that showed hypertolerance to As(III, V) was chosen for evaluating the metabolic perturbations during arsenic stress in both its oxidation states As(III) and As(V). Using NMR spectroscopy, we were able to identify and quantify an array of ∼45 metabolites, including amino acids, sugars, organic acids, phosphagens, osmolytes, nucleotides, etc. The NMR metabolomic experiments were complemented with various biophysical techniques to establish that the microalga tolerated the arsenic stress using a complex interplay of metabolites. The two different arsenic states distinctly influenced the microalgal cellular mechanisms due to their altered physicochemical properties. Eighteen differentially identified metabolites related to bioremediation of arsenic were then correlated to the major metabolic pathways to delineate the variable stress responses of microalga in the presence of As(III, V).
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| 19. |
- Arza, Carlos R., et al.
(författare)
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Synthesis, Thermal Properties, and Rheological Characteristics of Indole-Based Aromatic Polyesters
- 2019
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 4:12, s. 15012-15021
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Tidskriftsartikel (refereegranskat)abstract
- Currently, there is an intensive development of bio-based aromatic building blocks to replace fossil-based terephthalates used for poly(ethylene terephthalate) production. Indole is a ubiquitous aromatic unit in nature, which has great potential as a bio-based feedstock for polymers or plastics. In this study, we describe the synthesis and characterization of new indole-based dicarboxylate monomers with only aromatic ester bonds, which can improve the thermal stability and glass-transition temperature (Tg) of the resulting polyesters. The new dicarboxylate monomers were polymerized with five aliphatic diols to yield 10 new polyesters with tunable chemical structures and physical properties. Particularly, the Tg values of the obtained polyesters can be as high as 113 °C, as indicated by differential scanning calorimetry and dynamic mechanical analysis. The polyesters showed decent thermal stability and distinct flow transitions as revealed by thermogravimetric analysis and rheology measurements.
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| 20. |
- Asimi Neisiani, Ali, et al.
(författare)
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Technical and Economic Comparison between Sodium and Ammonium Agents in the Jarosite Precipitation Process─An Evaluation for Industrial Applications
- 2023
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Ingår i: ACS Omega. - : American Chemical Society. - 2470-1343. ; 8:39, s. 35442-36613
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Tidskriftsartikel (refereegranskat)abstract
- Iron content can cause severe challenges through zinc production from zinc sulfide concentrate. The zinc industry extensively uses the jarosite precipitation process (JPP) to precipitate dissolved iron and remove it before transferring the solution to downstream stages. Precipitating agents (PAs) play an essential role in the JPP. However, surprisingly, no study compares the efficiency of various PAs on an industrial scale. As an innovative approach, this investigation compares the technical and economic aspects of using various sodium and ammonium compounds (hydroxides, carbonates, bicarbonates, sulfates, and bisulfates) as typical PAs for the JPP at the Bafgh Zinc Smelting Company (BZSC) plant. Experimental results revealed that ammonium hydroxide, with 90.85% iron removal efficiency, had the highest performance, and sodium bisulfate and ammonium bisulfate had the lowest efficiency (74.54 and 77.13%, respectively). However, since ammonium hydroxide is a corrosive PA, it is not a promising alternative to sodium sulfate (with both economic and safety issues). Based on technical and economic assessments, sodium carbonate (84.31% iron removal efficiency) showed the highest potential for an efficient JPP.
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