Notes

Histone deacetylase hang-up contributes to regulation histone indicate changes and also impairs meiosis in oocytes.
The electrochemical Ni deposition at a platinum electrode was investigated in a plating nickel bath in the presence and absence of ethylene glycol (EG) using fluorescence yield soft X-ray absorption spectroscopy (FY-XAS) in the Ni L2,3-edge and O K-edge regions under potential control. At ≤+0.35 V vs. the reversible hydrogen electrode (RHE), the electrochemical Ni deposition was detected by the Ni L2,3-edge FY-XAS in the presence of EG whereas almost no such event was observed in the absence of EG. A drastic decrease of FY-XAS intensities in the O K-edge region was also observed in the presence of EG at >+0.35 V vs. RHE, suggesting that the nano-/micro-structured Ni deposition initiated by the removal of water molecules occurs on the Pt electrode. The complex formation of Ni2+ with EG and the adsorption of EG on the Ni surface could play an important role in the Ni deposition. This study demonstrates that the in situ FY-XAS is a powerful and surface-sensitive technique to understand (electro)chemical reactions including polyol synthesis and electrocatalysis at solid-liquid interfaces.The epoxy coating containing ZrO2 nanoparticles modified with 3-aminopropyltriethoxysilane (APTES) was prepared by electrostatic spraying on the surface of Q235 mild steel. The effect of the concentration of APTES-modified ZrO2 nanoparticles on the corrosion resistance of epoxy coating was characterized and tested by FTIR spectroscopy, scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). The results show that nano ZrO2 was successfully modified by a silane coupling agent. By adding an appropriate amount of APTES to modify nano ZrO2 in epoxy coating could significantly improve the corrosion resistance of the Q235 surface. When the mass fraction of nano ZrO2 is 2%, the composite coating shows the highest impedance value of about 1.0 × 105 Ω cm2 to achieve the best corrosion resistance.The use of hydrogen as an alternative fuel is an attractive and promising technology as it contributes to the reduction of environmentally harmful gases. Finding environmentally friendly cheap active metal-based catalysts for H2 rich syngas via dry reforming of methane (DRM) for industrial applications has posed a challenge. In this paper, H2 production via CO2 reforming of methane was investigated over 5Ni/ZrO2 catalysts. The catalytic performance of all prepared catalysts was evaluated in a microtubular fixed bed reactor under similar reaction conditions (i.e., activation temperature at 700 °C, feed flow rate of 70 ml min-1, reaction temperature 700 °C for 440 min reaction time) of CO2 reforming of methane. Different characterization techniques such as; BET, CO2-TPD, TGA, XRPD, Raman, and TEM, were used. The study of the textural properties of catalysts established that the BET of pristine catalyst (5NiZr) was enhanced by the addition of modifiers and promoters. A bimodal TPR distribution in the reduction temperature range of 250-550 °C was recorded. In the CO2-TPD analysis, the strength of basicity came in this order 5Ni15YZr > 5Ni10YZr > 5Ni5YZr > 5NiZr > 5Ni20YZr. The investigation of catalyst modifiers (MgO and Y2O3) resulted in the Y2O3 modifier improving the activity and catalytic performance better than MgO, which generated a hydrogen yield of 22%. 15% Y2O3 modifier loading gave the highest H2 yield 53% in the phase of different loadings of yttria. The study of the influence of promoters (Cs, Ga, and Sr) revealed that the catalytic performance of 5Ni15YZr catalysts promoted with Sr towards the H2 yield enhanced the activity to 62%. The promoted catalysts displayed lower carbon deposition compared to the unpromoted catalyst, which provided 25.6 wt% weight loss.Lignin is by far the most abundant natural renewable aromatic polymer in nature, and its reserves are second only to cellulose. In addition to the rich carbon content, the structure of lignin contains functional groups such as benzene rings, methoxyl groups, and phenolic hydroxyl groups. Lignin degradation has become one of the high value, high quality and high efficiency methods to convert lignin, which is of great significance to alleviating the current energy shortage and environmental crisis. read more This article introduces the hydrolysis methods of lignin in acidic, alkaline, ionic liquids and supercritical fluids, reviews the heating rate, the source of lignin species and the effects of heating rate on the pyrolysis of lignin, and briefly describes the metal catalysis, oxidation methods such as electrochemical degradation and photocatalytic oxidation, and degradation reduction methods using hydrogen and hydrogen supply reagents. The lignin degradation methods for the preparation of fuels and chemicals are systematically summarized. The advantages and disadvantages of different methods, the selectivity under different conditions and the degradation efficiency of different catalytic combination systems are compared. In this paper, a new approach to improve the degradation efficiency is envisioned in order to contribute to the efficient utilization and high value conversion of lignin.A series of core@shell SrTiO3@NiFe LDH composites (STONFs) were synthesized and their photocatalytic CO2 reduction performance was studied. The photocatalyst STONF 2 exhibited enhanced CO2 reduction performance with CO yield of 7.9 μmol g-1 h-1. The yield was 25.7 times and 8.8 times higher than that of NiFe LDH and SrTiO3 respectively, and also higher than most LDH based photocatalysts. Compared with two individual components, STONFs exhibited their combined merits of widened absorption spectrum, higher transportation efficiency and alleviated recombination of e-/h+ pairs. In addition, there were fewer oxygen vacancies in STONF 2 than as-prepared SrTiO3. Lower oxygen vacancies concentration would increase the opportunity of direct bonding between interface atoms of two components and successively increase the electron transportation and separation. These factors synergistically contributed to enhanced photocatalytic performance. This work will provide new insight for designing complementary multi-component photocatalysis systems.Three kinds of the bipyridine-proline chiral ligands as highly active species were successfully introduced on Zn-modified mesoporous silica nanomaterials (BMMs, MCM-41, and SBA-15) via the covalent attachment and coordination methods. Their microstructural features and physicochemical properties were extensively characterized via XRD patterns, SEM/TEM images, TGA profiles, FT-IR and UV-Vis spectra. In particular, their fractal features, the pair distance distribution function, and the Porod plots were evaluated thoroughly on the basis of the SAXS data. Meanwhile, their catalytic performances for asymmetric aldol reactions between p-nitrobenzaldehyde and cyclohexanone were evaluated. The results indicated that the bimodal mesoporous BMMs-based samples with short worm-like mesoporous channels possessed both mass and surface fractal features, whereas the MCM-41- and SBA-15-based samples with long-range ordered structures only showed surface fractal features. The influences of various reaction parameters, including the textures of the mesoporous silicas, the structures of the used chiral ligands, and the molecular volumes of aldehydes, on the catalytic activities (yield) and stereoselectivities (dr and ee) were investigated thoroughly. The results showed satisfactory activities (yields) and better stereoselectivity (dr and ee) in comparison with the homogeneous catalytic system using Z as the catalysts. In particular, the 3rd recycle catalytic performances of the Z-immobilized heterogeneous catalysts retained high catalytic yields (around 80%) and ee values of 28%. These phenomena were well interpreted by the essential relationships between the fractal characteristics of these heterogeneous catalysts and their catalytic activities.Among the cyclodextrins screened for the synthesis of 2-hydroxy-1,2-diphenylethanone (benzoin) in water, 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) exhibited the highest yield in the benzoin condensation reactions, and HP-β-CD can be recycled several times with little loss of activity through the addition of fresh VB1. As an example of supramolecular catalysis, the methodology was applied to the "green" synthesis of the antiepileptic drug phenytoin through benzoin condensation, oxidation, and cyclization reactions in the presence of HP-β-CD, without the use of any harmful organic solvent. Moreover, the complexation behaviors of HP-β-CD with benzaldehyde and intermediates were studied by UV-vis and 2D-ROESY NMR spectroscopies to reveal the plausible mechanisms of the reactions, and HP-β-CD did not act as a simple phase transfer agent.Removing salt from dye/salt mixtures using nanofiltration (NF) membranes needs to be improved to ensure high permeability, high selectivity, and antifouling performance. In this study, we used an interfacial polymerization (IP) technique to create a novel thin-film nanocomposite NF membrane by introducing two-dimensional MXene Ti3C2T x into the polyamide (PA) layer. Enhanced IP reaction rate facilitated the overflow of residual solvent from the fresh PA layer's edge due to the MXene-mediated IP strategy, resulting considerable bubble-like nodules on the membrane surface. The unique nanostructure of PA effective layer could be tuned by controlling the MXene concentration in aqueous phase solution, which finally promoted the obtained membranes with superb permselectivity. In this way, the water permeability was elevated to a maximum value of 45.12 L m-1 h-1, nearly 1.58-fold compared to the PA-pristine membrane. Moreover, the Ti3C2T x /NF membrane exhibited a superior dye/monovalent salt separation coefficient of 820, outperforming the pristine PA membrane and other NF membranes in the literature. Additionally, the MXene-assisted IP strategy designed an effective dye anti-fouling hydration layer, which played a crucial role in fouling resistance. This work illustrates a novel use of Ti3C2T x to successfully regulate high-performance TFN PA membranes for potential application in dye/salt separation.In the last decade, transition-metal-catalyzed direct C-H bond functionalization has been recognized as one of most efficient approaches for the derivatization of thioethers. Within this category, both mono- and bidentate-directing group strategies achieved the remote C(sp2)-H and C(sp3)-H functionalization of thioethers, respectively. This review systematically introduces the major advances and their mechanisms in the field of transition-metal-catalyzed remote C-H functionalization of thioethers from 2010 to 2021.The mechanical, electronic structure and optical properties of aluminium based double halide perovskite were calculated by density functional theory. The formation energy and elastic constant confirm the stability of the cubic perovskite materials. The materials are all ductile and suitable for flexible photovoltaic and optoelectronic devices. The band gap values vary from 0.773 eV to 3.430 eV, exactly corresponding to the range of ideal band gap values for good photoresponse. The band structure analysis shows that all the materials possess small effective mass, which indicates a good transport of carriers. And these materials have a broad energy range of optical absorption for utilization and a detector of photons. Moreover, less expensive K2AgAlBr6 were investigated for comparison with materials containing a cesium element, and according to the results, is also a candidate for photoelectronic devices due to the similar properties.
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