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91.
Elena S. Bobkova Dmitriy S. Krasnov Alexandra V. Sungurova Vladimir V. Rybkin Ho-Suk Choi 《Korean Journal of Chemical Engineering》2016,33(5):1620-1628
We studied phenol decomposition in aqueous solution under the action of DC discharge at atmospheric pressure in air. The decomposition efficiency was 0.017 molecules per 100 eV. When the kinetics of forming destruction products was studied in detail, the peculiarities of air plasma action were revealed for the first time. Plasma action not only results in the formation of oxygen-containing products, which are usually formed under oxygen plasma action (hydroxyhenols, carboxylic acids, aldehydes), but also the formation of nitro phenols. The treatment is accompanied by hydrogen peroxide formation, a pH decrease, and nitric and nitrous acids formation. We also discussed the possible mechanism of the processes and the role of some active species in chemical transformations after determining some parameters of the discharge. 相似文献
92.
Alexandr Valentinovich Vinogradov Vladimir Valentinovich Vinogradov 《Journal of the American Ceramic Society》2014,97(1):290-294
Nowadays, it is a great challenge to synthesize crystalline TiO2 nanostructures using low‐temperature methods without annealing stage. Such an approach allows to perform functional and structural modification in the formed crystalline phase by thermally unstable compounds, such as biomaterials, MOFs, dye sets in situ, which was previously considered impossible. In this work, we have developed and analyzed the effect of acidic peptization on formation of highly photoactive titania crystallites in an aqueous solution using titanium tetraisopropylate as a precursor. Acids with different dissociation degrees in water were used as peptizing mediators to determine the effect of protonation on sol formation. The dip‐coating films were obtained with consequent drying of the sols via evaporation of the solvent. The as‐prepared catalysts were characterized by X‐ray diffraction, AFM microscopy, UV–V is spectroscopy, Brunauer–Emmett–Teller surface area. The aggregate size of TiO2 in the colloidal suspension solution was measured by dynamic light scattering. Photocatalytic activity of films was studied by decomposition of Rhodamine B dye. It is found that the size of colloids in an aqueous solution is proportional to the protonation degree of the surface of particles and does not depend on the [Ti4+]/[H+] ratio, and peptization under weakly acidic conditions leads to anisotropic rod‐like nanoparticles. The highest photocatalytic activity was exhibited by the TiO2–HCl‐based coatings, ~3.5 times higher than that of the Acet.‐prepared sample. 相似文献
93.
Yanling Gao Vladimir V. Shvartsman Devendraprakash Gautam Markus Winterer Doru C. Lupascu 《Journal of the American Ceramic Society》2014,97(7):2139-2146
Dense nanocrystalline barium strontium titanate Ba0.6Sr0.4TiO3 (BST) ceramics with an average grain size around 40 nm and very small dispersion were obtained by spark plasma sintering at 950°C and 1050°C starting from nonagglomerated nanopowders (~20 nm). The powders were synthesized by a modified “Organosol” process. X‐ray diffraction (XRD) and dielectric measurements in the temperature range 173–313 K were used to investigate the evolution of crystal structure and the ferroelectric to paraelectric phase transformation behavior for the sintered BST ceramics with different grain sizes. The Curie temperature TC decreases, whereas the phase transition becomes diffuse for the particle size decreasing from about 190 to 40 nm with matching XRD and permittivity data. Even the ceramics with an average grain size as small as 40 nm show the transition into the ferroelectric state. The dielectric permittivity ε shows relatively good thermal stability over a wide temperature range. The dielectric losses are smaller than 2%–4% in the frequency range of 100 Hz–1 MHz and temperature interval 160–320 K. A decrease in the dielectric permittivity in nanocrystalline ceramics was observed compared to submicrometer‐sized ceramics. 相似文献
94.
Interpolyelectrolyte complexes of maleic acid copolymers and chitosan for stabilization and functionalization of magnetite nano‐ and microparticles 下载免费PDF全文
A facile method of preparation of stabilized and functionalized nano‐ and microparticles of magnetite by successive application of oppositely charged polymers with a regular structure of macromolecular chains (chitosan and maleic acid copolymers) onto Fe3O4 core are developed. This approach makes it possible to create two types of magnetite interpolyelectrolyte shells, containing carboxylic or amino groups in outer layer of shell. Composition and magnetic properties of composite particles depend on nature of the copolymer of maleic acid, reaction conditions and size of obtained particles. The carboxylic groups of copolymer in outer layer of interpolyelectrolyte shell were converted into reactive anhydride groups by heating. Thermal treatment also leads to covalent crosslinking of shell and improves stability of composites both in acidic and alkaline media. Horseradish peroxidase was successfully immobilized onto covalently crosslinked and activated microparticles of Fe3O4 in aqueous medium without of condensing agents. The proposed reproducible and low‐cost technique does not use toxic reagents or solvents at all stages, including preparation of Fe3O4, formation, activation and crosslinking, of magnetite shell, modification of activated surface of composite particles. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39663. 相似文献
95.
Electroactive behavior assessment of poly(acrylic acid)‐graphene oxide composite hydrogel in the detection of cadmium 下载免费PDF全文
Areli Bejarano‐Jiménez Vladimir A. Escobar‐Barrios J. Mieke Kleijn Cesar A. Ortíz‐Ledón Luis F. Cházaro‐Ruiz 《应用聚合物科学杂志》2014,131(19)
Super absorbent polymers of acrylic acid‐graphene oxide (PAA‐GO) were synthesized with different percentage of chemical neutralization (0, 10, and 20%) of the acrylic acid monomer before its polymerization. The influence of their swelling and adsorption/desorption capacity of cadmium ions in aqueous solutions were studied and revealed that the GO enables greater mechanical stability in the materials. The PAA hydrogels, with the same degrees of neutralization, were also prepared without GO to compare with the composites. Additionally, carbon paste electrodes (CPE) modified with the composites PAA‐GO were used to asses and compare their adsorption properties with cadmium(II). The anodic stripping voltammetry (ASV) peak, in the differential pulse voltammetry mode, for cadmium oxidation was found to be influenced by the presence of GO into the polymer, and also by their percentage of neutralization. The accumulation of cadmium(II) on the surface of the modified CPEs was performed under open‐circuit conditions taking an account the preconcentration time of the metal cation. The presence of GO enhances the electrical signal of the electrodes in short times of immersion in cadmium(II) solutions. This property contributed to get linear responses of the CPEs modified with the composites, which were influenced by their degrees of neutralization. The PAA‐GO 10N electrode with 10% of neutralization combined the influence of GO and the degree of neutralization in the same matrix, and also showed good performance in terms of its mechanical stability, it was chosen for preliminary studies on the selectivity of the electrode toward Zn(II) and Cu(II). © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40846. 相似文献
96.
Dina V. Dudina Igor S. Batraev Vladimir Yu. Ulianitsky Michail A. Korchagin 《Ceramics International》2014
This article is aimed to discuss the chemical aspects of detonation spraying of powder materials. In this method of coating deposition, ceramic, metallic or composite powders are injected into the barrel of a detonation gun filled with an explosive gaseous mixture. When the latter is ignited, the powders are heated and accelerated toward the substrate. Subjected to high temperatures, the powders are prone to chemical reactions, the reaction products possibly becoming the major phase constituents of the coatings. What types of reactions are possible? Can these reactions be carried out in a controlled manner? We answer these questions considering the interactions of the sprayed powders with the gaseous environment of the barrel as well as those between the phases of a composite feedstock powder. In Computer-Controlled Detonation Spraying (CCDS), the explosive charge and stoichiometry of the fuel-oxygen mixtures are precisely measured and can be flexibly changed. Our studies demonstrate that with the introduction of a highly flexible process of CCDS, detonation spraying has entered a new development stage, at which it can be considered as a powerful method of composition and microstructure tailoring of thermally sprayed coatings. During CCDS of TiO2-containing powders, chemical reduction of titanium dioxide can be carried out to different levels to form either oxygen-deficient TiO2−x or Ti3O5 suboxide. CCDS of Ti3Al can produce titanium oxide coatings when oxidation by the detonation products dominates or titanium nitride-titanium aluminide coatings when oxidation is hindered but the interaction of the powders with nitrogen—a carrier gas component—is favored. During detonation spraying of Ti3SiC2–Cu composites, the Ti3SiC2 phase is preserved only in cold conditions; otherwise, Si de-intercalates from the Ti3SiC2 phase and dissolves in Cu resulting in the formation of the TiCx–Cu(Si) composite coatings. 相似文献
97.
Alena Sergeeva Natalia Feoktistova Vladimir Prokopovic Dmitry Gorin Dmitry Volodkin 《Advanced Materials Interfaces》2015,2(18)
Fabrication of porous alginate hydrogels with a well‐controlled architecture useful for tissue engineering is still a challenge. Here, CaCO3‐based templating is utilized to design stable alginate gels with controlled pore dimensions in the range of 5–50 μm. The mechanism of pore formation is studied considering two factors affecting the pore size: i) osmotic pressure generated during the dissolution of sacrificial CaCO3 templates and ii) alginate gel network density. Osmotic pressure can achieve an upper limit of 100 MPa but does not affect the gel porosity. Additional osmotic pressure (range of kPa) induced by dextrans pre‐encapsulated into CaCO3 vaterite is also insufficient for pore enlargement. Pore stability depends merely on the gel network density and on the number of crosslinking calcium ions provided locally per unit time; pores are collapsed when template dissolution is too slow or if there is insufficient alginate concentration (below 2%). Young's modulus indicates the soft nature of the prepared hydrogels (tens of kPa) applicable as soft porous scaffolds with a tuned internal structure. 相似文献
98.
Melchior E. Evers Vladimir Titorenko Wim Harder Ida van der Klei Marten Veenhuis 《Yeast (Chichester, England)》1996,12(10):917-923
We have studied the role of flavin adenine dinucleotide (FAD) in the in vivo assembly of peroxisomal alcohol oxidase (AO) in the yeast Hansenula polymorpha. In previous studies, using a riboflavin (Rf) autotrophic mutant, an unequivocal judgement could not be made, since Rf-limitation led to a partial block of AO import in this mutant. This resulted in the accumulation of AO precursors in the cytosol where they remained separated from the putative peroxisomal AO assembly factors. In order to circumvent the peroxisomal membrane barrier, we have now studied AO assembly in a peroxisome-deficient/Rf-autotrophic double mutant (Δper1.rif1) of H. polymorpha. By sucrose density centrifugation and native gel electrophoresis, three conformations of AO were detected in crude extracts of Δper1.rif1 cells grown under Rf-limitation, namely active octameric AO and two inactive, monomeric forms. One of the latter forms lacked FAD; this form was barely detectable in extracts wild-type and Δper1 cells, but had accumulated in the cytosol of rif1 cells. The second form of monomeric AO contained FAD; this form was also present in Δper1 cells but absent/very low in wild-type and rif1 cells. In vivo only these FAD-containing monomers associate into the active, octameric protein. We conclude that in H. polymorpha FAD binding to the AO monomer is mediated by a yet unknown peroxisomal factor and represents the crucial and essential step to enable AO oligomerization; the actual octamerization and the eventual crystallization in peroxisomes most probably occurs spontaneously. 相似文献
99.
Mikhail V. Samsonov Nikita V. Podkuychenko Asker Y. Khapchaev Eugene E. Efremov Elena V. Yanushevskaya Tatiana N. Vlasik Vadim Z. Lankin Iurii S. Stafeev Maxim V. Skulachev Marina V. Shestakova Alexander V. Vorotnikov Vladimir P. Shirinsky 《International journal of molecular sciences》2022,23(1)
Hyperlipidemia manifested by high blood levels of free fatty acids (FFA) and lipoprotein triglycerides is critical for the progression of type 2 diabetes (T2D) and its cardiovascular complications via vascular endothelial dysfunction. However, attempts to assess high FFA effects in endothelial culture often result in early cell apoptosis that poorly recapitulates a much slower pace of vascular deterioration in vivo and does not provide for the longer-term studies of endothelial lipotoxicity in vitro. Here, we report that palmitate (PA), a typical FFA, does not impair, by itself, endothelial barrier and insulin signaling in human umbilical vein endothelial cells (HUVEC), but increases NO release, reactive oxygen species (ROS) generation, and protein labeling by malondialdehyde (MDA) hallmarking oxidative stress and increased lipid peroxidation. This PA-induced stress eventually resulted in the loss of cell viability coincident with loss of insulin signaling. Supplementation with 5-aminoimidazole-4-carboxamide-riboside (AICAR) increased endothelial AMP-activated protein kinase (AMPK) activity, supported insulin signaling, and prevented the PA-induced increases in NO, ROS, and MDA, thus allowing to maintain HUVEC viability and barrier, and providing the means to study the long-term effects of high FFA levels in endothelial cultures. An upgraded cell-based model reproduces FFA-induced insulin resistance by demonstrating decreased NO production by vascular endothelium. 相似文献
100.
Victor V. Dyakin Nuka V. Dyakina-Fagnano Laura B. Mcintire Vladimir N. Uversky 《International journal of molecular sciences》2022,23(1)
In humans, age-associated degrading changes, widely observed in molecular and cellular processes underly the time-dependent decline in spatial navigation, time perception, cognitive and psychological abilities, and memory. Cross-talk of biological, cognitive, and psychological clocks provides an integrative contribution to healthy and advanced aging. At the molecular level, genome, proteome, and lipidome instability are widely recognized as the primary causal factors in aging. We narrow attention to the roles of protein aging linked to prevalent amino acids chirality, enzymatic and spontaneous (non-enzymatic) post-translational modifications (PTMs SP), and non-equilibrium phase transitions. The homochirality of protein synthesis, resulting in the steady-state non-equilibrium condition of protein structure, makes them prone to multiple types of enzymatic and spontaneous PTMs, including racemization and isomerization. Spontaneous racemization leads to the loss of the balanced prevalent chirality. Advanced biological aging related to irreversible PTMs SP has been associated with the nontrivial interplay between somatic (molecular aging) and mental (psychological aging) health conditions. Through stress response systems (SRS), the environmental and psychological stressors contribute to the age-associated “collapse” of protein homochirality. The role of prevalent protein chirality and entropy of protein folding in biological aging is mainly overlooked. In a more generalized context, the time-dependent shift from enzymatic to the non-enzymatic transformation of biochirality might represent an important and yet underappreciated hallmark of aging. We provide the experimental arguments in support of the racemization theory of aging. 相似文献