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Abstract  

The present paper first establishes a decomposition result for f(x)∈ C r C r+1. By using this decomposition we thus can obtain an estimate of ∣f(x) - L n(f,x)∣ which reflects the influence of the position of the x's and ω(f (r+1),δ)j, j = 0,1,...,s, on the error of approximation.

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Maize seeds from inbred line Mo17, susceptible to Sugarcane mosaic virus (SCMV), were investigated for SCMV seed transmission. The seed quality significantly influenced the seed transmission rate. There were more infected seedlings derived from larger seeds than smaller seeds in both golden (G) and buff (B) seed groups, the proportion of infected seedlings in G1 was similar to G2 and B1, and significantly higher than the others (P < 0.05 or P < 0.01). While the proportion of SCMV seed transmission was higher in golden (3.9%) than buff seeds groups (2.3%), and there were significantly difference (P < 0.05) between the both colors seeds. However the percentage of infected seedlings was closely related to the location of seeds on ears, most infected seedlings were derived from seeds of the middle (Part III) and mid-base regions (Part IV), and the both parts (Parts III and IV) were significantly higher than that of Part I (P < 0.05). Fisher’s exact test indicated that the seed quality was associated significantly with the efficiency of SCMV seed transmission.

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Summary  

Adsorption microcalorimetry has been employed to study the interaction of ethylene with the reduced and oxidized Pt-Ag/SiO2catalysts with different Ag contents to elucidate the modified effect of Ag towards the hydrocarbon processing on platinum catalysts. In addition, microcalorimetric adsorption of H2, O2, CO and FTIR of CO adsorption were conducted to investigate the influence of Ag on the surface structure of Pt catalyst. It is found from the microcalorimetric results of H2and O2adsorption that the addition of Ag to Pt/SiO2leads to the enrichment of Ag on the catalyst surface which decreases the size of Pt surface ensembles of Pt-Ag/SiO2catalysts. The microcalorimetry and FTIR of CO adsorption indicates that there still exist sites for linear and bridged CO adsorption on the surface of platinum catalysts simultaneously although Ag was incorporated into Pt/SiO2. The ethylene microcalorimetric results show that the decrease of ensemble size of Pt surface sites suppresses the formation of dissociative species (ethylidyne) upon the chemisorption of C2H4on Pt-Ag/SiO2. The differential heat vs. uptake plots for C2H4adsorption on the oxygen-preadsorbed Pt/SiO2and Pt-Ag/SiO2catalysts suggest that the incorporation of Ag to Pt/SiO2could decrease the ability for the oxidation of C2H4.

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Abstract  

A new compound cyclohexyl-t-butyldimethylammonium tetraphenylborate, [C6H11N(CH3)2(C(CH3)3)]BPh4 has been prepared, and its decomposition mechanism was studied by TG. The IR spectra of the products of thermal decomposition were examined at every stage. Kinetic analysis for the first stage of thermal decomposition process was obtained by TG and DTG curves, and kinetic parameters were obtained from the analysis of the TG-DTG curves with integral and differential equations. The most probable kinetic function was suggested by comparison of kinetic parameters.

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Abstract  

The interaction between erythritol and 4-hexylresorcinol during heating was investigated by thermal analysis, powder X-ray diffractometry and infrared spectroscopy. A phase diagram was constructed by measuring the thermal behaviour of various resolidified physical mixtures of erythritol and 4-hexylresorcinol. The phase diagram revealed complex formation between erythritol and 4-hexylresorcinol with incongruent melting at 84C; the stoichiometry was a molar raio of 1:2 erythritol:4-hexylresorcinol. The complex gave diffraction peaks at 2θ=5.6 and 11.2 in the X-ray powder diffraction pattern. In the infrared spectrum, a new peak due to the complex was observed at 3504 cm–1. The complex prepared by grinding and evaporation had the same molecular arrangement as the complex prepared by sealed heating.

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This research was aimed to study the cell wall degradation and the dynamic changes of Ca2+ and related enzymes in developing aerenchyma of wheat root under waterlogging. An examination of morphological development by light and electron microscope revealed that the structure of cell wall in middle cortical cells remained intact after 12 h of waterlogging and turned thinner after waterlogging for 24 h. At 48 h, the aerenchyma has been formed. The cellulase activity gradually increased in middle cortical cells within 24 h of waterlogging, and decreased with the formation of aerenchyma. Fluorescence detection and subcellular localization of Ca2+ showed the dynamic changing of Ca2+ at the cellular and subcellular levels during the development of aerenchyma. The activity of Ca2+-ATPase enhanced markedly in intercellular space, plasma membrane and tonoplast of some middle cortical cells after 8 h of waterlogging and remained high after 24 h, but it decreased after 48 h of waterlogging. All these suggests that cellulase, Ca2+ and Ca2+-ATPase show a dynamic distribution during the aerenchyma development which associated with the cell wall degradation of middle cortical cells. Moreover, there is a feedback regulation between Ca2+ and Ca2+-ATPase.

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Summary

Dithiocarbamates fungicides (DTCs) are worldwidely used fungicides. Residue analytical methods on DTCs are usually based on headspace gas chromatography, which are not much stable and precise. In this study, a specific, simple and reliable method for determining DTCs fungicides residues was optimized and validated. The DTCs in foods and soils were extracted with an alkaline solution of EDTA and l-cysteine, followed by pH adjusting and methyl derivatization in methyl iodine solution. The organic layer of the reactants was separated, concentrated under vacuum and reconstructed in acetonitrile. DTCs residues were eluted on a C18 column and detected by HPLC-DAD at 272 nm. The S-alkyl derivatives of thiram, mancozeb and propineb were separated at different retention times. At fortified levels of 0.05 mg/kg to 2 mg/kg (residue expressed as CS2, in mg/kg, the same below), it is found that recoveries for DTCs spiked in apple, cucumber, tomato, rice and soil samples ranged from 70.8% to 105.3%, with relative standard deviations (RSD) from 0.6% to 13.7%. Limits of detection (LODs) and quantification (LOQs) ranged from 0.003 to 0.026 mg/kg and from 0.011 to 0.105 mg/kg for various foods and soils. This method was also applied to real sample tests.

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Journal of Radioanalytical and Nuclear Chemistry
Authors: D. Xu, Q. L. Ning, X. Zhou, C. L. Chen, X. L. Tan, A. D. Wu, and X. Wang

Summary  

Effects of ionic strength and of fulvic acid on the sorption of Eu(III) on alumina were investigated by using a batch technique. The experiments were carried out at T=25±1 °C, pH 4-6 and in the presence of 1M NaCl. The results indicate that sorption isotherms of Eu(III) are linear at low pH values. The sorption-desorption of Eu(III) on alumina at pH 4.4 is reversible, but a sorption-desorption hysteresis is found at pH 5.0. Fulvic acid has an obvious positive effect on the sorption of Eu(III) on alumina at low pH values. The migration of Eu(III) in alumina was studied by using column experiments and 152+154Eu(III) radiotracer at pH 3.8. For column experiments, Eu(III) sorbed on alumina can be desorbed completely from the solid surface at low pH values. The findings are relevant to the evaluation of lanthanide and actinide ions in the environment.

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A rapid and sensitive ultraperformance liquid chromatography-multiple reaction monitoring-multi-stage/mass spectrometry (UPLC-MRM-MS/MS) method has been developed for simultaneous quantification of salvianolic acid B and tanshinone IIA of salvia tropolone tablets in dog plasma. This was achieved by performing quantification using the MRM acquisition with two channels of MRM-MS/MS and MS full scan for more accuracy qualitative results, and the fragmentation transitions of m/z 295→249, 191 for tanshinone IIA and m/z 297→279, 251 for IS in positive mode, m/z 717→519, 321 for salvianolic acid B and m/z 295→267, 239 for IS in negative mode were selected. The UPLC separation was achieved within 3 min in a single UPLC run. Linear calibration curves were obtained over the concentration range of 10 pg/mL−1 ng/mL for tanshinone IIA and 100 pg/mL−1 for salvianolic acid B. Lower limit of quantitation (LLOQ) was 10 pg/mL and 100 pg/mL for tanshinone IIA and salvianolic acid B, respectively. The inter-day and intra-day precision (relative standard deviation, RSD) in all samples were less than 8.21%, and the recoveries were over 85.9% for both tanshinone IIA and salvianolic acid B. The two channels of MRM with MS full scan approach could provide both qualitative and quantitative results without the need for repetitive analyses and resulted in the reduction of further confirmation experiments and analytical time. The pharmacokinetic study of the two active components of salvia tropolone tablets following oral gavage administration of dogs was thus explored with this method.

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The inhibitory effects of phytic acid (PA) on the browning of fresh-cut chestnuts and the associated mechanisms of PA on polyphenol oxidase (PPO) and peroxidase (POD) activities were investigated. The enzymatic browning of chestnut surfaces and interiors was suppressed by soaking shelled and sliced chestnuts in a PA solution. The specific activities of PPO and POD extracted from chestnuts declined due to inhibition by PA. PA was determined to be a competitive inhibitor of both PPO and POD by Lineweaver-Burk plots. The binding modes of PA with PPO and POD were analysed by AutoDock 4.2.

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