Evaluation of system codes for analyzing naturally circulating gas loop

Steady-state natural circulation data obtained in a 7 m-tall experimental loop with carbon dioxide and nitrogen are presented in this paper. The loop was originally designed to encompass operating range of a prototype gas-cooled fast reactor passive decay heat removal system, but the results and conclusions are applicable to any natural circulation loop operating in regimes having buoyancy and acceleration parameters within the ranges validated in this loop. Natural circulation steady-state data are compared to numerical predictions by two system analysis codes: GAMMA and RELAP5-3D. GAMMA is a computational tool for predicting various transients which can potentially occur in a gas-cooled reactor. The code has a capability of analyzing multi-dimensional multi-component mixtures and includes models for friction, heat transfer, chemical reaction, and multi-component molecular diffusion. Natural circulation data with two gases show that the loop operates in the deteriorated turbulent heat transfer (DTHT) regime which exhibits substantially reduced heat transfer coefficients compared to the forced turbulent flow. The GAMMA code with an original heat transfer package predicted conservative results in terms of peak wall temperature. However, the estimated peak location did not successfully match the data. Even though GAMMA's original heat transfer package included mixed-convection regime, which is a part of the DTHT regime, the results showed that the original heat transfer package could not reproduce the data with sufficient accuracy. After implementing a recently developed correlation and corresponding heat transfer regime map into GAMMA to cover the whole range of the DTHT regime, we obtained better agreement with the data. RELAP5-3D results are discussed in parallel.     

Identification of Novel Pepper Genes Involved in Bax- or INF1-Mediated Cell Death Responses by High-Throughput Virus-Induced Gene Silencing

Hot pepper is one of the economically important crops in Asia. A large number of gene sequences, including expressed sequence tag (EST) and genomic sequences are publicly available. However, it is still a daunting task to determine gene function due to difficulties in genetic modification of a pepper plants. Here, we show the application of the virus-induced gene silencing (VIGS) repression for the study of 459 pepper ESTs selected as non-host pathogen-induced cell death responsive genes from pepper microarray experiments in Nicotiana benthamiana. Developmental abnormalities in N. benthamiana plants are observed in the 32 (7%) pepper ESTs-silenced plants. Aberrant morphological phenotypes largely comprised of three groups: stunted, abnormal leaf, and dead. In addition, by employing the combination of VIGS and Agrobacterium-mediated transient assays, we identified novel pepper ESTs that involved in Bax or INF1-mediated cell death responses. Silencing of seven pepper ESTs homologs suppressed Bax or INF1-induced cell death, five of which suppressed both cell death responses in N. benthamiana. The genes represented by these five ESTs encode putative proteins with functions in endoplasmic reticulum (ER) stress and lipid signaling. The genes represented by the other two pepper ESTs showing only Bax-mediated cell death inhibition encode a CCCH-type zinc finger protein containing an ankyrin-repeat domain and a probable calcium-binding protein, CML30-like. Taken together, we effectively isolated novel pepper clones that are involved in hypersensitive response (HR)-like cell death using VIGS, and identified silenced clones that have different responses to Bax and INF1 exposure, indicating separate signaling pathways for Bax- and INF1-mediated cell death.     

Synthesis of boron nitride nanotubes using thermal chemical vapor deposition of ball milled boron powder

Thermal chemical vapor deposition (TCVD) produces relatively pure boron nitride nanotubes (BNNTs), while it may not be enough for production. A ball milling–annealing process is beneficial in quantity; however, the generation of the impurity is most concerned. In this regard, we explored the dual syntheses of BNNTs based on the chemical reactions of solid and gaseous boron with nitrogen, respectively. Synthesis mechanisms for both were also analyzed by presenting the stepwise reaction routes. With these understandings, the production of BNNTs could be increased, while the impurities are reduced when compared with the individual one, once the experimental conditions are optimized.     

Synthesis and decomposition performance of a polymeric foaming agent containing a sulfonyl hydrazide moiety

A new monomer, methacryloyloxybis(benzenesulfonyl hydrazide) (MAOBSH) containing a foamable sulfonyl hydrazide functional group after decomposition by heating, was synthesized from 4,4′‐oxybis(benzenesulfonyl hydrazide) (OBSH) with methacryloyl chloride, and used to obtain poly(MAOBSH) as a polymeric foaming agent (PFA) in dry tetrahydrofuran at 70 °C using azobisisobutyronitrile as an initiator. The structures of the synthesized MAOBSH and poly(MAOBSH) were identified using Fourier transform infrared and ¹ H NMR spectroscopies. The decomposition temperature of poly(MAOBSH) was determined to be 245 °C and this temperature was decreased to around 160 °C by adding an activator such as surface‐treated urea to the polymer. The exothermic temperature and heat determined by the decomposition of the polymer were 256 °C and 287 J g^?1. The amount of gas evolution for poly(MAOBSH) measured at the decomposition temperature was 74 mL g^?1. Furthermore, polymers incorporating the PFA showed better skin and finer cell structure as well as better mechanical properties such as elongation and compression set than polymers with added OBSH due to the better compatibility of the developed PFA with polymers. © 2012 Society of Chemical Industry     

Ruthenium(II)‐ or Rhodium(III)‐Catalyzed Grignard‐Type Addition of Indolines and Indoles to Activated Carbonyl Compounds

The ruthenium(II)‐ or rhodium(III)‐catalyzed pyrimidinyl‐directed Grignard‐type C−H additions of N‐heterocycles with activated aldehydes and ketones are described. A cationic ruthenium catalyst and sodium acetate additive in dichloroethane as solvent were found to be optimal catalytic system for the construction of C‐7 alkylated indolines. In sharp contrast, a cationic rhodium complex allows the generation of C‐2 alkylated indoles and pyrroles as well as C‐1 alkylated carbazoles. The site‐selective C−H functionalization of these heterocyclic scaffolds could be an important asset towards the development of novel bioactive compounds.

     

Design and validation of a high-throughput matrix-assisted laser desorption ionization time-of-flight mass spectrometry method for quantification of hepcidin in human plasma

Disorders of iron metabolism affect over a billion people worldwide. The circulating peptide hormone hepcidin, the central regulator of iron distribution in mammals, holds great diagnostic potential for an array of iron-associated disorders, including iron loading (β-thalassemia), iron overload (hereditary hemochromatosis), and iron deficiency diseases. We describe a novel high-throughput matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry assay for quantification of hepcidin in human plasma. This assay involves enrichment using a functionalized MALDI chip, a novel solvent-detergent precipitation buffer, and quantification using a stable isotope labeled internal standard. The linear range of hepcidin in plasma was 1-120 nM, with a low limit of quantification (LOQ) (1 nM), high accuracy (<15% relative error (RE)), and high precision (intraday average 5.52-18.48% coefficient of variation (CV) and interday 9.32-14.83% CV). The assay showed strong correlation with an established hepcidin immunoassay (Spearman; R(2) = 0.839 n = 93 ethylenediaminetetraacetic acid (EDTA) plasma). A collection of normal healthy pediatric samples (range 3.8-32.5 ng/mL; mean 12.9 ng/mL; n = 119) showed significant differences from an adult collection (range 1.8-48.7 ng/mL; mean 16.1 ng/mL; n = 95; P = 0.0096). We discuss these preliminary reference ranges and correlations with additional parameters in light of the utility and limitations of hepcidin measurements as a stand-alone diagnostic and as a tool for therapeutic intervention.     

Photoluminescence characteristics of Li-doped CaTiO3:Pr thin films grown on Si (100) substrate by PLD

The effects of Li-doped CaTiO₃:Pr³⁺ thin films have been investigated by varying the lithium ion concentrations from 0 to 5 wt.%. The films have been deposited on Si (100) substrate using a pulsed laser deposition technique. Structural properties of these films have been studied by the measurement of their XRD, SEM, and AFM. The variation of Li⁺ concentration influences the crystallinity and surface morphology of the CaTiO₃:Pr³⁺ thin films. As Li⁺ content increases from 0 to 1 wt.%, the crystallinity and intensity of emission increases. The dominant emission is from ¹D₂ → ³H₄ transition at 613 nm. The ¹D₂ emission quenching has also been observed in highly doped sample and is related to the cross-relaxation process between Pr³⁺ ions.     

Microstructure and mechanical properties of quaternary Cr–Si–O–N films by a hybrid coating system

Quaternary Cr–Si–O–N films were deposited by a hybrid coating system using a Cr cathodic arc target and a Si sputtering target in an Ar/N₂/O₂ gaseous mixture. The influence of oxygen flux rate on the microstructure and properties of the Cr–Si–O–N films were investigated. The results indicated that the oxygen-free Cr–Si–N film exhibited nanocolumnar microstructure containing CrN nano columns and amorphous Si₃N₄ phase. The Cr–Si–O–N films exhibit equiaxed CrN nanocrystallites likely surrounded by amorphous SiO₂ and Si₃N₄ phases. Further increasing the oxygen content gives films containing Cr₂O₃ crystallites. The hardness first increases from 30 GPa for the Cr–Si–N film to a maximum value of approximately 50 GPa for the oxygen content of 16 at.% and then decreases for larger oxygen content. All the Cr–Si–O–N films exhibit low friction coefficient (0.22–0.26) and low residual stress (− 0.03–0.08 GPa). The influence of the oxygen content on the microstructure and mechanical properties of the Cr–Si–O–N films is discussed.