The (Z)-4-aryliden-2-(2-acetoxyphenyl)-5(4H)oxazolones 1a-1c react with H2SO4 to give the corresponding (Z)4-aryliden-2-(2-hydroxyphenyl)-5(4H)oxazolones *** molecular structures of 1c and 2a have been determined by X...
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The (Z)-4-aryliden-2-(2-acetoxyphenyl)-5(4H)oxazolones 1a-1c react with H2SO4 to give the corresponding (Z)4-aryliden-2-(2-hydroxyphenyl)-5(4H)oxazolones *** molecular structures of 1c and 2a have been determined by X-ray diffraction methods, and show planar skeletons. Oxazolones 2a-2c are potential c,N,Otridentate ligands towards transition metals, and their molecular design obeys to the search of a rigid environment around the metal. The reaction of Pd(OAc)2 with oxazolones 2a-2c (1:1 M ratio) in cF3cO2H or NcMe as solvents results in the synthesis of diverse complexes (3-7). As a function of the reaction conditions, two different bonding modes have been characterized: N,O-chelate in the dinuclear complexes [Pd(kappa 2-N,O-2b,c)(mu -O2ccF3)]2 (3b,c), as a result of the N-coordination and deprotonation of the hydroxy group;and c,N,Otridentate in mononuclear complexes [Pd(kappa 3-c,N,O-2a,b)(L)] (L = cF3cO2H 4a,b;dmso-d6 5a,b;NcMe 6b;pyridine 7b), obtained after N-bonding, OH deprotonation and c-H bond activation. All complexes have been fully characterized by HRMS and NMR methods, showing the high stability of the c,N,O-tridentate bonding mode.
The Nicr-cr3c2-caF2/BaF2 coating with the NiAl bond coating was sprayed on a Ni16cr13co4Mo(wt%) alloy by detonation-gun spray, and hot corrosion behaviors were studied by electrochemical measurements. In molten Nacl-K...
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The Nicr-cr3c2-caF2/BaF2 coating with the NiAl bond coating was sprayed on a Ni16cr13co4Mo(wt%) alloy by detonation-gun spray, and hot corrosion behaviors were studied by electrochemical measurements. In molten Nacl-Kcl, the corrosion products were mainly cr2O3. Gas phases such as cl2 led to spallations and cracks on the coating surface. In molten Nacl-Na2SO4, Na2SO4 decomposed and reacted with the coating. Mixed oxides formed a continuous corrosion layer, and Al diffused outward from bond coating to be oxidized. Some liquid phases existed in the corrosion layer and promoted hot corrosion. The detailed hot corrosion mechanisms in two molten salts were discussed.
The hydroxyapatite (HA) coating on carbon/carbon (c/c) is reasonable and feasible to obtain bone graft materials with appropriate mechanical and biological properties. However, improvement of the physical and chemical...
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The hydroxyapatite (HA) coating on carbon/carbon (c/c) is reasonable and feasible to obtain bone graft materials with appropriate mechanical and biological properties. However, improvement of the physical and chemical properties of HA-c/ccomposites to promote bone regeneration and healing remains a challenge. In our present study, the HA coatings on c/c with magnesium (Mg) (Mg-HA-c/c) composites were synthesized that ca (NO3)(2), Mg (NO3)(2), and NH4H2PO4 were mixed and coatings were made by electromagnetic induction deposition's heating. As determined with in vitro experiments, Mg-HA-c/ccomposites containing 10 and 20% Mg decreased miR-16 levels, increased cell viability, elevated the levels of osteogenesis-related genes, and promoted osteogenic differentiation of bone marrow mesenchymal stem cells (BMScs) seeded on their surfaces. In a rat model of skull defects, compared to the control group, at 4 and 12 weeks after the operation, the bone volume fraction (BV/TV) of Mg-HA-c/ccomposite group was increased by 8.439 +/- 2.681% and 23.837 +/- 7.845%, as well as the trabecular thickness (***) was 56.247 +/- 24.238 mu m and 114.911 +/- 34.015 mu m more. These composites also increased the levels of ALP and RUNX2 in skull. The Mg-HA-c/ccomposite-enhanced bone regeneration and healing were blocked by in situ injection of an miR-16 mimic lentivirus vector. Thus, Mg-HA-c/ccomposites promote osteogenic differentiation and repair bone defects through inhibiting miR-16.
In this paper, for the first time, simultaneous atmospheric temperature perturbation profiles obtained from the TIMED/SABER satellite and equatorial ion density and vertical plasma drift velocity observations with and...
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In this paper, for the first time, simultaneous atmospheric temperature perturbation profiles obtained from the TIMED/SABER satellite and equatorial ion density and vertical plasma drift velocity observations with and without ESF activity obtained from the c/NOFS satellite are used to investigate the effect of gravity waves (GW) on ESF. The horizontal and vertical wavelengths of ionospheric oscillations and GWs are estimated by applying wavelet analysis techniques. In addition, vertically propagating GWs that dissipate energy in the ionosphere-thermosphere system are investigated using the spectral analysis technique. We find that the vertical wavelength of GW, corresponding to dominant wavelet power, ranges from 12 to 31 km regardless of the conditions of the ionosphere;however, GWs with vertical wavelengths between about 1 to 13 km are found every day, saturated between 90 and 110 km at different longitudinal sectors. Filtering out vertical wavelengths above 13 km from temperature perturbations, ranges of zonal wavelengths of GW (i.e., from about 290 to 950 km) are found corresponding to irregular and non-irregular ionosphere. Similarly, corresponding to dominant oscillations, the zonal wavelength of ion density perturbations is found within 16 to 1520 km. Moreover, we find an excellent agreement among the median zonal wavelengths of GW for the cases of irregular and non-irregular ionosphere and ion density perturbations that are 518, 495, and 491 km, respectively. The results imply that seed perturbations due to GW with a vertical wavelength from about 1 to 13 km evolve to ion density irregularity and may be amplified due to post-sunset vertical upward drift velocity.
In order to optimize the degradation of high-concentration aniline wastewater, the operation of sequencing batch bioaugmentation reactors with different aniline concentrations (200 mg/L, 600 mg/L, 1000 mg/L) was studi...
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In order to optimize the degradation of high-concentration aniline wastewater, the operation of sequencing batch bioaugmentation reactors with different aniline concentrations (200 mg/L, 600 mg/L, 1000 mg/L) was studied. The results showed that the removal rates of aniline and cOD in the three reactors could reach 100%. When the aniline increased to 600 mg/L, the nitrogen removal efficiency reached the peak (51.85%). The increase of aniline inhibited the nitrification, while denitrification was enhanced due to the increase of c/N ratio. But this change was reversed by the toxicity of high concentrations of aniline. The metagenomic analysis showed that when the aniline concentration was 600 mg/L, the abundance distribution of microbial samples was more uniform. The improved of aniline concentration had led to the increase of aromaticcompounds degradation metabolic pathways. In addition, the abundance of aniline degradation and nitrogen metabolism genes (dmpB, xylE, norB) was also promoted.
The high temperature oxidation mechanisms of grain refined Fe-25Al-1.5Ta (at%) with Tac or (Ta,Nb)c additives were investigated at 700 ? in air for 503 h to study the influence of microstructural changes on the oxidat...
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The high temperature oxidation mechanisms of grain refined Fe-25Al-1.5Ta (at%) with Tac or (Ta,Nb)c additives were investigated at 700 ? in air for 503 h to study the influence of microstructural changes on the oxidation behaviour. While a thin and stable alpha-Al2O3 scale was formed at the Fe-Al matrix, additional phases were selectively oxidised leading to higher oxidation kinetics of Fe-25Al-1.5Ta with carbide additives. The selectively oxidised c14 (Fe,Al)2Ta Laves phase showed the formation of outer Fe2O3 and an inner (Al,Ta)-rich oxide, while Al-rich oxides were found along the (Al,Ta)-rich oxide/Fe-Al phase boundary and locally below Fe2O3.
In this study, a combined system with simultaneous nitrification, denitrification, and phosphorus removal was operated in continuous low oxygen aeration mode, and the effect of lower oxygen aeration (dissolved oxygen ...
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In this study, a combined system with simultaneous nitrification, denitrification, and phosphorus removal was operated in continuous low oxygen aeration mode, and the effect of lower oxygen aeration (dissolved oxygen [DO] 0.5-1.5 mg/L) on its performance was examined. The combined system consisted of sludge and high-efficiency biological packing and was operated using four carbon/nitrogen ratios (c/N) with being 10:1, 8:1, 6:1, 10:1. Experimental results showed that the combined system could perform an efficient nitrogen and phosphorus removal under low DO and c/N ratio of 8:1 condition, and removal efficiencies of chemical oxygen demand (cOD), NH4 (+)-N, and PO4 (3-)-P were 80.01%, 99.03%, and 89.51%, respectively. High-throughput analysis indicated that the functional species of denitrifying bacteria, including Ferruginibacter Azospira, comamonas, Bacilli, Hyphomicrobium, Thauera, and comamonadaceae, were important participants in biological nutrient removal. Meanwhile, Acinetobacter was enriched in the combined system, which contributed to phosphorus removal. Practitioner Points A combined system was operated firstly under continuous low oxygen condition. The lower dissolved oxygen (DO) of the combined system was maintained at 0.50-1.5 mg/L level. The combined system could realize simultaneous phosphorus and nitrogen removal under c/N ratio of 8:1. Several functional bacteria were enriched in the coupled systems.
Developing a conductive and corrosion-resistant coating on metal bipolar plates is essential to mitigate the degradation induced by the high cathodic transient potentials of proton exchange membrane fuel cells. In thi...
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Developing a conductive and corrosion-resistant coating on metal bipolar plates is essential to mitigate the degradation induced by the high cathodic transient potentials of proton exchange membrane fuel cells. In this work, a multilayer nanoscale c/Ti coating is prepared on SS316L (c/Ti/SS). The c/Ti/SS achieves a highly prominent IcR of 1.59 m omega cm2 and corrosion rate of 2 x 10-8 A/cm2, remarkably better than the targets. Analysis of coating microstructure and composition suggests that the significantly enhanced corrosion resistance is attributed to the diffusional interfaces which optimize the potential distribution across the coating and improve the transpassive potential of c/Ti/SS.
Innovative nanocomposites consisting of [(GeTe)(4 nm/)c-1 nm](10) multilayers (MLs) deposited by magnetron sputtering are integrated in phase-change memory (PcM) test devices with a "wall structure." Scannin...
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Innovative nanocomposites consisting of [(GeTe)(4 nm/)c-1 nm](10) multilayers (MLs) deposited by magnetron sputtering are integrated in phase-change memory (PcM) test devices with a "wall structure." Scanning transmission electron microscopy (STEM) shows that an ML structure, with crystallized GeTe layers, is kept after integration in as-fabricated devices and also after an additional annealing of the devices at 425 degrees c. The programming current (RESET current) required to reach the high resistance state of [(GeTe)(4 nm)/c-1 nm](10) ML devices decreases by 45% after annealing at 425 degrees c. The reduction in RESET current is 55% and the reduction in drift coefficient is about 40% in ML devices annealed at 425 degrees ccompared to similar devices incorporating Ge2Sb2Te5. STEM imaging, coupled with nano-beam electron diffraction and electron energy loss spectroscopy, of ML devices in the high resistance state shows that the RESET current reduction after annealing is correlated to a reduction of the amorphized volume.
Electrochemical cO2 reduction to valuable multi-carbon (c2+) products is attractive but with poor selectivity and activity due to the low-efficient c-ccoupling. Herein, a lithium vacancy-tuned Li2cuO2 with square-pla...
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Electrochemical cO2 reduction to valuable multi-carbon (c2+) products is attractive but with poor selectivity and activity due to the low-efficient c-ccoupling. Herein, a lithium vacancy-tuned Li2cuO2 with square-planar [cuO4] layers is developed via an electrochemical delithiation strategy. Density functional theory calculations reveal that the lithium vacancies (V-Li) lead to a shorter distance between adjacent [cuO4] layers and reduce the coordination number of Li+ around each cu, featuring with a lower energy barrier for cO-cO coupling than pristine Li2cuO2 without V-Li. With the V-Li percentage of approximate to 1.6%, the Li2-xcuO2 catalyst exhibits a high Faradaic efficiency of 90.6 +/- 7.6% for c2+ at -0.85 V versus reversible hydrogen electrode without iR correction, and an outstanding partial current density of -706 +/- 32 mA cm(-2). This work suggests an attractive approach to create controllable alkali metal vacancy-tuned cu catalytic sites toward c2+ products in electrochemical cO2 reduction.
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