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Polyelectrolyte microspheres find applications in many fields such as ion exchange columns, fuel cell membranes, and catalysis, to name a few. Synthesis of these microspheres by inverse emulsion polymerization offers various advantages due to the increased specific surface area and high surface charge density. The surface charge density of the obtained polyelectrolyte microspheres is a hundred times higher than that of either particles obtained by dispersion copolymerization of styrene and styrenesulfonic acid or sulfonated microspheres. The morphology, chemical structure, and electro-surface properties of the synthesized microspheres were studied by transmission and scanning electron microscopy, FTIR-spectroscopy, and conductometric and potentiometric titrations, respectively. Using the potentiometric titration it is possible to characterize the structure of the surface layer of polyelectrolyte microspheres as entirely as possible. The study of the ion-exchange capacity of polyelectrolyte microspheres shows that ion-exchange capacity is 2.1 meq g-1 in this case, which is more than 2 times higher than that of sulfonated microspheres, and 20 times higher than that of particles obtained by dispersion copolymerization.Measurement of heat capacity of superionic silver sulfide (argentite β-Ag2S) revealed that nanocrystalline argentite has a higher heat capacity than coarse-crystalline argentite. It is shown that the heat capacity of nanocrystalline substances includes an additional positive contribution caused by the limitation of the phonon spectrum on the part of low and high frequencies due to a small particle size. The estimation of this contribution on the basis of experimental differences in the heat capacities of nano- and coarse-crystalline argentite β-Ag2S in the region of its existence, 470-850 K, made it possible to determine for the first time the velocities of propagation of longitudinal and transverse elastic vibrations cl and ct and elastic stiffness constants c11, c12 and c44. It is established that with a rise in temperature the elastic characteristics of argentite decrease. The anisotropy of elastic properties of cubic argentite was analyzed, and the crystal lattice directions corresponding to the largest and the least values of elastic moduli were determined. An increase of the temperature from 470 to 850 K leads to a small decrease of the elastic anisotropy of cubic β-Ag2S argentite.The development of carbon materials for potassium storage is limited by their low specific capacity and poor cycling stability due to the sluggish kinetics of K ions. Herein, fucoidan-derived oxygen-rich carbon nanosheets are reported as a fantastic anode for potassium ion batteries. Attributed to its 2D porous sheet-like structure (morphology engineering), rich oxygen doping (defect engineering), and dilated graphitic layer in an amorphous structure (structure engineering), a competitive capacity of 392 mA h g-1 at 0.05 A g-1 and a long cycling span over 2500 cycles at 2 A g-1 was achieved for the carbon anode, outperforming most of the reported carbons. The kinetic analyses reveal that rich active sites and a porous nanosheet structure account for the superb rate performance and cycling stability of the material. Ex situ X-ray photoelectron spectroscopy measurements demonstrate that the introduction of C[double bond, length as m-dash]O greatly promotes K+ adsorption, and that the improvement of the C[double bond, length as m-dash]O bonds during cycling contributes to enhancement in the capacity. The fabricated potassium ion hybrid capacitor displays an exceptional energy/power density of 193 W h kg-1/22 324 W kg-1, and a promising cycling stability with 99.3% capacity retention over 2000 cycles. This work provides a large-scale synthesis strategy for preparing oxygen-rich carbon nanosheets for advanced potassium ion storage.The Prins cyclization of styrene (SE) with paraformaldehyde (PFCHO) was conducted with mesoporous ZnAlMCM-41 catalysts for the synthesis of 4-phenyl-1,3-dioxane (4-PDO) using a liquid phase heterogeneous catalytic method. For a comparison study, the Prins cyclization reaction was also conducted over different nanoporous catalysts, e.g. mesoporous solid acid catalysts, AlMCM-41(21) and ZnMCM-41(21), and microporous catalysts, USY, Hβ, HZSM-5, and H-mordenite. The recyclable mesoporous ZnAlMCM-41 catalysts were reused in this reaction to evaluate their catalytic stabilities. Since ZnAlMCM-41(75) has higher catalytic activity than other solid acid catalysts, washed ZnAlMCM-41(75)/W-ZnAlMCM-41(75) was prepared using an efficient chemical treatment method and used with various reaction parameters to find an optimal parameter for the highly selective synthesis of 4-PDO. W-ZnAlMCM-41(75) was also used in the Prins cyclization of olefins with PFCHO and formalin (FN, 37% aqueous solution of formaldehyde (FCHO)) under different reaction conditions to obtain 1,3-dioxanes, which are widely used as solvents or intermediates in organic synthesis. Based on the nature of catalysts used under different reaction conditions, a reasonable plausible reaction mechanism for the Prins cyclization of SE with PFCHO is proposed. Notably, it can be seen from the catalytic results of all catalysts that the W-ZnAlMCM-41(75) catalyst has higher 4-PDO selectivity with exceptional catalytic activity than other microporous and mesoporous catalysts.Visceral fat is a more important factor in obesity-associated disorders in Japanese individuals than in Caucasian individuals. Pidnarulex The objective of this randomised, double-blind, placebo-controlled parallel group study, conducted in Japanese overweight adults, was to investigate the effects of polymethoxyflavone purified from Kaempferia parviflora on visceral fat. A total of 80 subjects (aged 20-64 years, 23.0 ≤ body mass index less then 30 kg m-2) were randomly assigned in 1  1 ratio to either the active (polymethoxyflavone purified from K. parviflora) or placebo group. Over a 12-week period, each subject received two capsules containing polymethoxyflavone purified from K. parviflora (12 mg polymethoxyflavone per day) or placebo. The primary outcome was a reduction in visceral fat area (VFA), while the secondary outcome was a reduction in subcutaneous fat area (SFA) and total fat area (TFA). VFA was measured at 0, 8, and 12 weeks using computed tomography scanning. Results showed that VFA significantly reduced after 12 weeks in the active group and was significantly lower than in the placebo group at 8 and 12 weeks.