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Quantitative aftereffect of subretinal water along with intraretinal hydropsy in aesthetic skill in uveitic cystoid macular swelling.
The effects of flipping membranes with hydrophilic/hydrophobic asymmetry are well documented in the literature, but not much is known on the impact of flipping a membrane with dense/porous layer asymmetry. In this work, the pure water flux (PWF) of a commercial polyethersulfone (PES) membrane and a ceramic ultrafiltration (UF) membrane was measured in the normal and inverted positions. Our experimental results showed that the PWF was two orders of magnitude higher when the PES membrane was flipped to the inverted position, while the increase was only two times for the ceramic membrane. The filtration experiments were also carried out using solutions of bovine serum albumin and poly(vinylpyrrolidone). A mathematical model was further developed to explain the PWF increase in the inverted position based on the Bernoulli's rule, considering a straight cylindrical pore of small radius connected to a pore of larger radius in series. It was found by simulation that a PWF increase was indeed possible when the solid ceramic membrane was flipped, maintaining its pore geometry. The flow from a layer with larger pore size to a layer with smaller pore size occurred in the backwashing of the fouled membrane and in forward and pressure-retarded osmosis when the membrane was used with its active layer facing the draw solution (AL-DS). find more Therefore, this work is of practical significance for the cases where the direction of the water flow is in the inverted position of the membrane.Novel inorganic-organic hybrid membranes Fe@MWCNT/PPO or Fe@MWCNT-OH/SPPO (with a new type of CNTs characterized by increased iron content 5.80 wt%) were synthesized for CO2 separation. The introduction of nanofillers into the polymer matrix has significantly improved the hybrid membrane's gas transport (D, P, S, and αCO2/N2), magnetic, thermal, and mechanical parameters. It was found that magnetic casting has improved the alignment and dispersion of Fe@MWCNTs. At the same time, CNTs and polymer chemical modification enhanced interphase compatibility and the membrane's CO2 separation efficiency. The thermo-oxidative stability and mechanical and magnetic parameters of composites were improved by increasing new CNTs loading. Cherazi's model turned out to be suitable for describing the CO2 transport through analyzed hybrid membranes.Ionic liquids (ILs) have a wide variety of applications in modern electrochemistry due to their unique electrolytic properties. In particular, they are promising candidates as dopants for polymeric membranes in potentiometric sensors and liquid-junction free reference electrodes. However, the effective use of ILs requires a comprehensive understanding of their electrolytic behavior in the polymeric phase. We report here the exploration of the electrolytic and diffusion properties of IL 1-hexyl-3-methyl-1H-imidazol-3-ium bis[(trifluoromethyl)sulfonyl]amide ([C6Meim][NTf2]) in a poly(vinyl chloride) matrix. Chronopotentiometry is utilized to determine the concentration of charge carriers, ionic diffusion coefficients and apparent dissociation constant of [C6Meim][NTf2] in PVC membranes plasticized with a mixture of [C6Meim][NTf2] and bis(2-ethylhexyl) sebacate (DOS) over a wide range of IL concentrations. The diffusion properties of [C6Meim][NTf2] are confirmed by NMR-diffusometry. The non-monotonic electrolytic behavior of the IL in PVC-DOS matrix is described for the first time. A maximum ionization degree and diffusion coefficient is observed at 30 wt.% of IL in the plasticizing mixture. Thus, it is shown that by varying the flexible parameter of the IL to plasticizer ratio in the polymeric phase one can tune the electrolytic and transport properties of sensing PVC membranes.The antimicrobial peptide magainin 2 (M2) interacts with and induces structural damage in bacterial cell membranes. Although extensive biophysical studies have revealed the interaction mechanism between M2 and membranes, the mechanism of membrane-mediated oligomerization of M2 is controversial. Here, we measured the synchrotron-radiation circular dichroism and linear dichroism (LD) spectra of M2 in dipalmitoyl-phosphatidylglycerol lipid membranes in lipid-to-peptide (L/P) molar ratios from 0-26 to characterize the conformation and orientation of M2 on the membrane. The results showed that M2 changed from random coil to α-helix structures via an intermediate state with increasing L/P ratio. Singular value decomposition analysis supported the presence of the intermediate state, and global fitting analysis revealed that M2 monomers with an α-helix structure assembled and transformed into M2 oligomers with a β-strand-rich structure in the intermediate state. In addition, LD spectra showed the presence of β-strand structures in the intermediate state, disclosing their orientations on the membrane surface. Furthermore, fluorescence spectroscopy showed that the formation of β-strand oligomers destabilized the membrane structure and induced the leakage of calcein molecules entrapped in the membrane. These results suggest that the formation of β-strand oligomers of M2 plays a crucial role in the disruption of the cell membrane.In the context of global warming, clean energy represented by fuel cells has ushered in a window period of rapid development; however, most research mainly focuses on the improvement of catalysts and performance, and there is very little research on the performance differences and energy consumption between different oxidants. In this paper, the performance differences of fuel cells with different oxidants (air and oxygen) are studied using a self-made CCM, and the economic aspect is calculated from the perspective of power improvement and energy consumption. Firstly, the CCM and GDL are prepared, and the hydrophilicity and hydrophobicity of GDL are realized by the addition of PTFE and SiO2, respectively. Secondly, through the experiment, it is found that the fuel cell can achieve the best comprehensive performance at 60 °C, and the use of oxygen can achieve the highest power increase, 117.1%, compared with air. Finally, from the perspective of economics, after excluding the power consumed for preparing oxygen, the use of oxygen as an oxidant still achieved a net power increase of 29.512%. The research in this paper clearly shows that using oxygen instead of air can greatly improve performance and is good economically, which makes it a useful exploration for the research of fuel cells.In order to lengthen the life cycle of packaging materials, it is essential to study their potential for reuse. This has been never carried out for emerging bio-based and biodegradable materials such as PHBV/(ligno-)cellulosic fibre-based biocomposite materials. This work therefore highlights the impact of successive dishwashing cycles on the physical-chemical and structural stability of such materials. Several parameters were considered to assess this stability, such as the visual aspect and colour, the microstructure, the thermal and tensile properties, and the overall migration in food liquid simulants. The effect of fibre composition, morphology, and content was investigated by selecting three types of commercial (ligno-)cellulosic fibres and two filler contents (20 and 40 wt%). A great potential for reuse of PHBV films was highlighted by their high stability after up to at least 50 dishwashing cycles. However, the addition of (ligno-)cellulosic fillers negatively impacts the stability of PHBV-based materials, especially due to the hygroscopic behaviour of (ligno-)cellulosic fillers and the heterogenous microstructure of biocomposites, with at best up to 10 possible dishwashing cycles for ultra-pure cellulose. In conclusion, reuse including dishwashing steps can be considered for neat PHBV materials, while this should be prohibited for PHBV/(ligno-)cellulosic fibre-based biocomposite materials.Bioelectrochemical systems are emerging technologies for the reduction in CO2 in fuels and chemicals, in which anaerobic chemoautotrophic microorganisms such as methanogens and acetogens are typically used as biocatalysts. The anaerobic digestion digestate represents an abundant source of methanogens and acetogens microorganisms. In a mixed culture environment, methanogen's inhibition is necessary to avoid acetate consumption by the presence of acetoclastic methanogens. In this study, a methanogenesis inhibition approach based on the thermal treatment of mixed cultures was adopted and evaluated in terms of acetate production under different tests consisting of hydrogenophilic and bioelectrochemical experiments. Batch experiments were carried out under hydrogenophilic and bioelectrochemical conditions, demonstrating the effectiveness of the thermal treatment and showing a 30 times higher acetate production with respect to the raw anaerobic digestate. Moreover, a continuous flow bioelectrochemical reactor equipped with an anion exchange membrane (AEM) successfully overcomes the methanogens reactivation, allowing for a continuous acetate production. The AEM membrane guaranteed the migration of the acetate from the biological compartment and its concentration in the abiotic chamber avoiding its consumption by acetoclastic methanogenesis. The system allowed an acetate concentration of 1745 ± 30 mg/L in the abiotic chamber, nearly five times the concentration measured in the cathodic chamber.The application of graphene oxide (GO)-based membranes combined with a quartz crystal microbalance (QCM) as a humidity sensor has attracted great interest over the past few years. Understanding the influence of the structure of the GO membrane (GOM) on the adsorption/desorption of water molecules and the transport mechanism of water molecules in the membrane is crucial for development of applications using GOM-based humidity sensors. In this paper, by investigating the effects of oxygen-containing groups, flake size and interlayer spacing on the performance of humidity sensing, it was found that humidity-sensing performance could be improved by rational membrane-structure design and the introduction of magnesium ions, which can expand the interlayer spacing. Therefore, a novel HGO&GO&Mg2+ structure prepared by uniformly doping magnesium ions into GO&HGO thin composite membranes was designed for humidity sensing from 11.3% RH to 97.3% RH. The corresponding sensor exhibits a greatly improved humidity sensitivity (~34.3 Hz/%RH) compared with the original pure GO-based QCM sensor (~4.0 Hz/%RH). In addition, the sensor exhibits rapid response/recovery times (7 s/6 s), low hysteresis (~3.2%), excellent repeatability and good stability. This research is conducive to understanding the mechanism of GOM-based humidity sensors. Owing to its good humidity-sensing properties, the HGO&GO&Mg2+ membrane-based QCM humidity sensor is a good candidate for humidity sensing.Forward osmosis membranes have a wide range of applications in the field of water treatment. However, the application of seawater desalination is restricted, so the research of forward osmosis membranes for seawater desalination poses new challenges. In this study, zeolitic imidazolate framework-8 (ZIF-8) was synthesized by a mechanical stirring method, and its crystal structure, surface morphology, functional group characteristics, thermochemical stability, pore size distribution and specific surface area were analyzed. The cellulose acetate (CA)/ZIF-8 mixed matrix forward osmosis membrane was prepared by using the synthesized ZIF-8 as a modified additive. The effects of the additive ZIF-8 content, coagulation bath temperature, mixing temperature and heat treatment temperature on the properties of the CA/ZIF-8 forward osmosis membrane were systematically studied, and the causes were analyzed to determine the best membrane preparation parameters. The structure of the CA membrane and CA/ZIF-8 mixed matrix forward osmosis membranes prepared under the optimal conditions were characterized by Fourier Transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), contact angle and Atomic force microscope (AFM).
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