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The synergistic effect between MoOx and Fe markedly promoted the activity on deoxygenation of lactic acid to bio-propionic acid.

Background: Previous studies have shown that TIFA (TNF receptor associated factor (TRAF)-interacting protein with a Forkhead-associated (FHA) domain) plays different roles in various tumor types. However, the function of TIFA in colorectal cancer (CRC) remains unclear. The goal of this study is to uncover the biological function and molecular mechanism of TIFA in CRC.Methods: Tissue microarrays were used to evaluate TIFA expression. Cancer cell proferation assays were performed in TIFA knockdown and overexpressing cells in vitro and in a xenograft model in vivo. Human phosphokinase array, immunoprecipitation assays were performed to explore the underlying mechanism.Results: We disclosed that the expression of TIFA was marked increased in CRC versus normal tissue, and positively correlated with CRC TNM stages. In agreement, we found that the CRC cell lines show increased TIFA expression levels versus normal control. The knockdown of TIFA inhibited cell proliferation but have no effects on cell apoptosis in vitro and in vivo. Moreover, the ectopic expression of TIFA enhanced cell proliferation ability in vitro and in vivo. In contrast, the expression of mutant TIFA (T9A, oligomerization site mutation; D6, TRAF6 binding site deletion) alternatively abolished TIFA mediated cell proliferation enhancement. Exploration of the underlying mechanism demonstrated that the protein synthesis associated kinase RSK and PRAS40 activation were all responsible for TIFA mediated CRC progression. Conclusions: The above results described a model of TIFA in mediating CRC progression. This may provide a promising target for CRC therapy.

Plant diseases reduce crop yield and quality, hampering the development of agriculture. Fungicides, which restrict chemical synthesis in fungi, are the strongest controls for plant diseases. However, the harmful effects on the environment due to continued and uncontrolled utilization of fungicides have become a major challenge in recent years. Plant-sourced fungicides are a class of plant antibacterial substances or compounds that induce plant defenses. They can kill or inhibit the growth of target pathogens efficiently with no or low toxicity, they degrade readily, and do not prompt development of resistance, which has led to their widespread use. In this study, the growth inhibition effect of 24 plant-sourced ethanol extracts on rice sprigs was studied. Ethanol extract of gallnuts and cloves inhibited the growth of bacteria by up to 100%. Indoor toxicity measurement results showed that the gallnut and glove constituents inhibition reached 39.23 μg/mL and 18.82 μg/mL, respectively. Extract treated rice sprigs were dry and wrinkled. Gallnut caused intracellular swelling and breakage of mitochondria, disintegration of nuclei, aggregation of protoplasts, and complete degradation of organelles in hyphae and aggregation of cellular contents. Protection of Rhizoctonia solani viability reached 46.8% for gallnut and 37.88% for clove in water emulsions of 1000 μg/mL gallnut and clove in the presence of 0.1% Tween 80. The protection by gallnut was significantly stronger than that of clove. The data could inform the choice of plant-sourced fungicides for the comprehensive treatment of rice sprig disease. The studied extract effectively protected rice sprigs and could be a suitable alternative to commercially available chemical fungicides. Further optimized field trials are needed to effectively sterilize rice paddies.

Plant diseases reduce crop yield and quality, hampering the development of agriculture. Fungicides, which restrict chemical synthesis, are the strongest controls for plant diseases. However, the harmful effects on the environment due to continued and uncontrolled utilization of fungicides has become a major challenge in recent years. Plant-sourced fungicides are a class of plant antibacterial substances or compounds that induce plant defenses. They can kill or inhibit the growth of target pathogens efficiently with no or low toxicity, degrade readily, do not prompt development of resistance, which has led to their widespread use. In this study, the growth inhibition effect of 24 plant-sourced ethanol extracts on rice sprigs was studied. Ethanol extract of gallnuts and cloves inhibited the growth of rice sprites by up to 100%. Indoor toxicity measurement results showed that the gallnut and glove constituents inhibition reached 39.23 μg/mL and 18.82 μg/mL, respectively. Extract treated rice sprigs were dry and wrinkled. Gallnut caused intracellular swelling and breakage of mitochondria , disintegration of nuclei, aggregation of protoplasts, and complete degradation of organelles in hyphae and aggregation of cellular contents. Protection of Rhizoctonia solani viability reached 46.8% for gallnut and 37.88% for clove in water emulsions of 1,000 μg/mL gallnut and clove in the presence of 0.1% Tween 80. The protection by gallnut was significantly stronger than that of clove. The data could inform the choice of plant-sourced fungicides for the comprehensive treatment of rice sprig disease. The studied extract effectively protected rice sprigs and could be a suitable alternative to commercially available chemical fungicides. Further optimized field trials are needed to effectively sterilize rice paddies.

A new method is proposed to solve edge cracking and corrosion in rolling process of the magnesium alloy plate. Usually in the process, the edge cracking is caused by the great temperature difference between the edge and the center of the alloy plate and the corrosion is by water in air. The method uses hot air wrapped around the plate to perfectly prevent edge cracking and corrosion. The method also includes cathodic protection for the magnesium alloy based on electrochemistry. The suppression of cathodic protection on the chemical activity of the magnesium alloy was studied. The experiment shows that the new method of edge heating with hot air wrapping is effective to prevent edge cracking and corrosion. Also, the cathodic protection can effectively suppress the chemical activity of the magnesium alloy and improve the surface quality in the rolling process of the magnesium plate, which provides a new concept in rolling process of the magnesium alloy.

To design and synthesize materials for alkaline hydrogen evolution is favorable for industrial hydrogen cycle operation. In this study, we present a facile approach to synthesize free-standing ruthenium-beryllium (RuBe) nanosheets, which possess amorphous phase state and associated with holey structures due to the molten method. The two-dimensional RuBe nanosheets exhibit improved activity than pure Ru counterpart and comparable properties to commercial Pt toward hydrogen evolution reaction in both of alkaline and neutral electrolytes. Based on the experiments and density functional theory calculations, it is suggested that the adsorption and dissociation of water molecules on Ru-based catalyst are much enhanced with the assistance of Be modulation, which are essential for the improved hydrogen production capability under alkaline condition. This work broadens the Ru-based catalyst family and may provide new insights for electrocatalyst development.

Reduced graphene oxide wrapped hollow molybdenum trioxide nanorods (MoO 3 @rGO) have been fabricated by a facile process. The MoO 3 @rGO shows improved lithium storage performance. It could deliver a high reversible capacity (842 mAh/g at 0.1 A/g), excellent cycling stability (778 mAh/g at 0.1 A/g after 200 cycles) and excellent rate capability (455 mAh/g at 2 A/g). The excellent electrochemical performance could be attributed as the special core (MoO 3 )/sheath (rGO) structure, which could accommodate the volume change of MoO 3 during lithiation/delithiation process. In addition, the rGO coating layer could improve the electronic conductivity of MoO 3 .

Heteroatom-doped carbon nanomaterials with well-defined porous are used as anode materials for SIBs due to their exceptional structural characteristics. In this work, porous N-doped carbon networks composed with ultrathin carbon nanosheets were synthesized via the direct pyrolysis of Vitamin B5. The content of nitrogen, specific surface area, porous structure of the N-doped carbon nanosheet networks were adjusted by changing reaction temperatures. The formation mechasim of the ultrathin N-doped carbon nanosheet networks was also proposed. The generation of calcium carbonate/calcium oxide used as a self-template renders the formation of the porous structure via thermal treatment. The optimized samples possess a superior lithium and sodium storage: 1534 mAh g −1 at 100 mA g −1 vs. Li/Li + and 335 mAh g −1 at 100 mA g −1 vs. Na/Na + , with nearly 100% cycling Coulombic efficiency, remarkable cycling retention and high rate capacity. Additionally, good electrocatalytic activity for ORR via a 4e −1 pathway determines that the resulting primary Zn-air battery showed high discharge power energy density (80 mW cm −2 ), high reversibility and stability over continuous cycles.

The photoluminescence (PL) and circularly polarized luminescence (CPL) of ((R)-1-phenyl-N-(pyren-1-ylmethyl)ethanamine) P-R were successfully modulated via fine-tuning and precise control of excited conformation of dimer/excimer by external stimuli. The resulting aggregation-induced emission (AIE)-active material (P-R) exhibited CPL with a low dissymmetry factor (∼10−4) in monomeric form, while demonstrating a prominent CPL signal with a higher dissymmetry factor (∼10−3) in thin solid films even without annealing processes.

Germanium (Ge) has been considered as a promising anode material for Li-ion batteries because of its theoretical capacity (1600 mA h g−1). However, its poor electrochemical performances resulting from the large volume variation during Li–Ge alloy/dealloy processes prevent its practical application. Herein, we designed a 3D core/shell structure by encapsulation of Ge in a sulfur (S) and nitrogen (N) co-doped three-dimensionally (3D) interconnected macroporous carbon matrix (denoted as Ge@S,N-3DPC). The 3D porous structure can not only buffer the volume change during alloy/dealloy processes, but also facilitate the electrolyte to soak in, offering fast ion/electron pathways. What's more, the co-doping of S and N in carbon could introduce more defects and active sites, which can also help to improve the interfacial adsorption and electrochemical behaviors. When used as an anode material for LIBs, the Ge@S,N-3DPC shows excellent electrochemical performances (1000 mA h g−1 at 200 mA g−1), outstanding cycling stability (94% capacity retention after 300 cycles) and high rate capability (358 mA h g−1 at 10 A g−1). This work develops a general strategy to improve the electrochemical performance of these alloy-type electrode materials with huge volume change in the energy storage area.

Solvent-dependent self-assemblies of an amphiphilic molecule based on perylene bisimide were employed in the fabrication of well-defined millimeter long nanorods and high density nanofibers, respectively. Moreover, the fabricated memory device demonstrated good behaviours with a low operating voltage, high ON/OFF ratio, long retention time, and good stability.

The Sb encapsulated in S and N co-doped three-dimensionally (3D) interconnected macroporous carbon composite (denoted as Sb@S,N-3DPC) has been fabricated by using silica opals as hard template following a carbonization process. The structural and morphological characterizations reveal the uniform 3D-network structure with the Sb nanoparticles embedded homogeneously in the carbon spherical shell. The Sb@S,N-3DPC electrode shows a high reversible capacity of 482 mAh g −1 at 100 mA g −1 , displaying good capacity stability (~93% of the initial discharge capacity after 500 cycles at 100 mA g −1 ). The electrode displays superior rate capability and ultralong cyclability (255 mAh g −1 at 2 Ag −1 after 2000 cycles) and also reveals a good rate capability that maintains 160 mAh g −1 at 5 Ag −1 . The excellent electrochemical performance of the Sb@S,N-3DPC is attributed to the 3D-porous carbon network structure and uniform distribution of Sb nanoparticles in carbon matrix, enhancing the conductivity, holding the structure integrity, and thus improving the cycling performance of the anode material. In addition, sulfur and nitrogen co-doping introduced more defects and active sites to the carbon framework, thereby improving the interfacial adsorption and electrochemical behaviors.

Treatment of 1,2-C6H4(SiH3)(SiH3) (1) with Pt(dcpe)(PEt3)2 (dcpe = Cy2PCH2CH2PCy2) in dry toluene at room temperature in the ratio of 1:1 leads to the complex {1,2-C6H4(SiH2)(SiH2)}PtII(dcpe) (2), which can react with proton organic reagent bearing hydroxy group with low steric hindrance to form a tetra-alkoxy substituted silyl platinum(II) compound (3). The structures of complexes (2) and (3) were unambiguously determined by multinuclear NMR spectroscopic studies and single crystal X-ray analysis.

A novel set of multifunctional optically active π-conjugated polymers incorporating perylenyl moieties, were designed and synthesized. Chirality transfer and amplification from chiral unit to the main-chain backbone in dilute solution was achieved, which was closely related to the stereocenter in the pendant of a π-conjugated polymer. In addition, annealed films of these polymers exhibited near-infrared emission by direct absorption of visible light, resulting from the introduction of a strong fluorophore perylenyl moiety. Such a design strategy opens up new perspectives for the future development of novel optically active materials with near-infrared emission for photonic applications.

The plant Na+/H+ antiporter (NHX) plays a significant role in cellular ion homeostasis. Herein, an Na+/H+ antiporter gene, SpNHX1 from the Sesuvium portulacastrum plant, was obtained by homology-cloning method. The SpNHX1 gene contains 2113 bp with an open-reading frame encoding a polypeptide of 554 amino acid residues with an estimated molecular mass of 61.27 kDa and an isoelectric point of 7.24. The amino acid sequences of SpNHX1 shared a high similarity with Arabidopsis thaliana AtNHX1 (75.81%), AtNHX2 (77.12%) and Oryza sativa OsNHX1 (73.10%). SpNHX1 contains an amiloride-binding region (FFIYLLPPI), which is a highly-conserved domain in plant Na+/H+ antiporters. RT-PCR (reverse transcriptional PCR) analysis showed that the SpNHX1 gene had a high expression level in roots compared to other tissues under normal conditions. The qRT-PCR (quantitative real-time PCR) results indicated that NaCl treatment induced the expression of SpNHX1 gene in the roots, but its transcriptional levels were not influenced by the ABA, PEG, H2O2, heat (42 °C) or cold (4 °C) stresses. The growth of yeast cells expressing SpNHX1 was better than the non-transgenic control cells in the presence of 30 mM NaCl, 0.4 M KCl, or 0.5 mM LiCl. Furthermore, transgenic yeast cells with SpNHX1 accumulated more Na+ relative to control cells under salinity stress. These results suggested that SpNHX1 was a key determinant in the salt-stress response in Sesuvium portulacastrum.

Stimuli-responsive circularly polarized luminescence (CPL) was successfully achieved through fine-tuning the conformation of a perylenyl dyad by using external stimuli. Monomer CPL was clearly detected from an inherent achiral monochromophore system in a simple perylene–carbazole dyad, and concentration-dependent CPL was observed from ‘good solvent’, giving an excimer-like CPL emission with a peak maximum at 643 nm. Moreover, the CPL bands depended on the aggregated state, which was identical to the emission changes in the THF–H2O system. It is noteworthy that the perylene–carbazole dyad emitted efficient CPL in thin films even without annealing processes. The specific perylenyl–carbazole structure plays a crucial role in CPL in response to the external environment. This novel molecular design strategy opens up a new perspective for the future development of smart CPL-active organic dyads.

A hollow cathode configuration was designed for a Grimm-type glow discharge atomic emission spectrometer (GD-AES). The operating conditions including the hollow cathode dimension, applied pulsed voltage and argon pressure, were optimized. The 10-μs pulses at 1.8 kV in a 3-torr discharge worked best. A pulsed hollow cathode Grimm discharge (HCG) offers several advantages: efficient excitation and ionization; high sensitivity; temporal spectral resolution; and rapid sample interchange. The capability of this source for the determination of elemental composition in metals, alloys and in solution residues is investigated. Samples used in this study included copper and steel standards.

The already established technique of pulsed glow discharge spectroscopy is extended in these studies to the application of a second pulse applied at a variable delay after a first pulse. The net discharge then consists of a series of double pulses in which each second pulse in the series enhances the emission intensity of the analyte atoms produced by the first pulse. A copper hollow cathode is used to show high emission enhancement for atom and ion lines of the sputtered species and the neon discharge gas species. The technique shows promise for further study by both atomic emission and mass spectrometry.

3D hierarchical flower-like carbon coated MoO3−x nanosheets (denoted as MoO3−x NS@C) have been successfully fabricated by a simple hydrothermal method. When used as anode for Li-ion batteries, the MoO3−x NS@C electrode exhibits excellent cycle performance and outstanding rate capabilities. The charge capacity can reach 1025 mAh g−1 over 150 cycles, and 62% of the charge capacity is retained when the current density increases to 2000 mA g−1. The improved lithium storage performance of MoO3−x NS@C is attributed to the synergistic effect of oxygen vacancies and the carbon coating, which not only enhance the electric conductivity and Li-ion diffusion coefficient but also lead to superior structural stability and cyclability of the MoO3−x NS@C electrode during repeated lithiation/delithiation process.

The development of microsecond pulsed glow discharge atomic emission spectrometry (GD-AES) for quantitative depth profile analysis is described. The quantification method, which is based on sputtering rates, has been previously applied to depth analysis employing a dc glow discharge source. Optimal conditions of the glow discharge source, including voltage, pressure, pulse width and pulse frequency, are utilized in order to give the best depth resolution. Pulsed operation of the glow discharge affords the advantages of two additional parameters, pulse width and pulse frequency, which allow better control over the amount of sample being removed via cathodic sputtering. This allows thin layer samples to be analyzed that are very difficult using the dc source. Under the optimized parameters, thin coatings of varying depths of Cu deposited on steel were quantified. The quantitative method predicted Cu deposition depths in accord with the nominal depths.

A Grimm-type glow discharge ion source has been constructed for a time-of-flight mass spectrometer (TOF-MS). This source was operated in the microsecond-pulsed mode. Special features of pulsed Grimm GD-TOF-MS are described, including resolving power, stability, sensitivity and the temporal separation of discharge gas species and analyte ions. The analytical characteristics of a pulsed Grimm GD-TOF-MS system were also evaluated. These preliminary studies demonstrate the potential of this technique for the elemental analysis for solids.

A high voltage, microsecond regime, pulsed glow discharge has been applied to a standard Grimm type source on a LECO SA-2000 multichannel optical spectrometer. The spectrometer system has been equipped with fast time-resolved electronics in order to study the temporal response of the elemental emission lines. The aim of the research was to investigate possible gains in signal-to-background ratio (S/B) and detection limits compared to a conventional direct current (dc) mode of operation. It was found that the high instantaneous pulse power in itself gives approximately a factor 2 increase in S/B. By utilising time-resolved detection, gains in the range 5–10 are achieved. For nitrogen, it was found that the background from leakage of air could be reduced to approximately 1/3 compared with the dc mode. Another interesting observation was that certain nearly non-conducting materials, which cannot be run in dc mode, could be run in the microsecond pulsed mode.

A high voltage, microsecond regime pulse dc glow discharge was applied to a standard Grimm source on a modified LECO SA-2000 direct reader spectrometer and to a duplicate Grimm source coupled to a scanning monochromator. The effects of experimental conditions, including pulse voltage, pulse frequency, pulse width and Ar pressure, on Cu atomic and ionic emission intensities were examined and compared with continuous discharge results. The pulsed Grimm source has a higher sputtering rate, greater signal intensity and lower detection limits. The pulsed signal for atomic lines shows a different temporal response from ionic lines. Pulsed Grimm GD-AES also offers control features advantageous in the measurement of thin surface layers.

A thermospray nebulizer was used as a sample introduction device for microwave plasma torch (MPT) atomic emission spectrometry (AES). Experimental parameters, including the power supplied to the MPT, the flow rates of support and carrier gases, the observation height, the sample uptake rate, the thermospray working temperature, the temperature of the aerosol spray chamber and cooling water were optimized. Under optimum conditions, the relative standard deviation (RSD) of 10 measurements for 21 elements is in the range 0.3–2.0%. The detection limits were improved in comparison with the ultrasonic nebulizer as sample introduction technique for MPT–AES. The inclusion of 20% methanol into the MPT showed there is no effect on the stability of MPT discharge. The technique can thus be held to have the potential for interface to reverse-phase HPLC systems.

A transient data acquisition system for flow injection analysis (FIA), high performance liquid chromatography (HPLC), and electrothermal vaporization (ETV) combined with ICP-AES multi-element instrumentation was developed and successfully applied to the analysis of different types of samples, including human serum, human hair and tea, for simultaneous multi-element determinations. The accuracy of the method was verified with hair reference material. Good agreement between the experimental results and certified values, and also satisfactory recoveries from standard additions, were achleved.

Palladium salts can be used as a coprecipitation carrier for the preconcentration of trace elements from natural water prior to their measurement by atomic spectrometry (AAS). The palladium is subsequently reduced by the introduction of hydrogen gas into the sample solution. The procedure is applied to the determination of Cu, Pb and Cd in seawater (enrichment factor 50) and synthetic water samples. Operating conditions have been optimized for the analysis of real samples. With the technique established an enrichment factor (500 fold) is feasible in synthetic samples. The recoveries of Cu, Cd and Pb from seawater are 95, 103 and 100%, respectively. This simple and rapid method can be applied in a wide pH-range and with complex matrices.

Over 100 hair samples were collected from the Xiamen area of south China, including 72 healthy people and 34 cancer patients, for the study of distinguishing cancer patients from others; another 64 hair samples were collected from patients with liver, stomach, lung, and miscellaneous cancers and were used for the discrimination analysis of different types of cancers, The samples were analyzed with ICP-AES for the simultaneous determination of several elements and with GFAAS for Se content after wet digestion. The average values of the element concentrations in the hair samples are presented. The results obtained were then analyzed with principal component analysis and partial least-squares methods, to distinguish cancer patients from others, and with an orthaganolization recurrence method to discriminate different types of cancers. The cancer patients could be completely distinguished from healthy people; while the misdiscrimination rates for the analysis of liver, stomach, and lung cancers are 15.8, 14.3, and 19.0%, respectively.

The application of microsecond pulsed Grimm glow discharge atomic emission spectrometry for depth profiling of thin films is examined. The effects of pulsed conditions including pulse voltage, pulse frequency, pulse width, and Ar pressure on depth profiling performance were characterized for Zn and Cu coatings on steel. Using optimized conditions, linear calibration curves of coating thickness for Zn (6.1-26.9 μm) and Cu (50-500 nm) on steel were achieved. A precision of 2-5% relative standard deviation was determined. An ultrathin coating of Cu (10 nm) on steel was also measured by this technique.

A Grimm-type glow discharge ion source, operated in the microsecond pulsed mode, has been interfaced to a commercial time-of-flight mass spectrometer. Ion transport from the source to the mass spectrometer, an inherent limitation of a Grimm source and mass spectrometer combination, was evaluated. The primary discharge operating conditions found to influence transport efficiency were gas flow rate and source pressure. The configuration of the Grimm-type source also influenced ion transport, including use of a gas-directing sleeve device. The effect of transport efficiency was separated into two components: (1) total ion signal and (2) temporal resolution. The latter is an advantage afforded by use of a pulsed glow discharge source and time-of-flight spectrometer, which allows discrimination against interfering gaseous background ions by appropriate ion sampling time. Shown as an example is the identification of trace magnesium from potential background interference using an optimized source configuration based on this temporal resolution method.

In this paper, a thin-disk laser with the output power of kW level is demonstrated. The laser used is Nd:YAG laser medium for easiness to reach the threshold power densities of the pump and less heat to dissipate from the crystal. The thin disk of 1 mm thickness with 1.5-at. % Nd doped and a simple 4-pass pump coupling system is designed to fulfill the total absorption of the pump light. 2D-stacks diode array works as the pump source and a conventional optics is used for efficient and uniform pumping.

Pulsing the glow discharge offers new experiments and applications with a well-established technique.