小麦分离合子与幼胚中膜钙和钙调素的分布

用非酶手工显微解剖法分离小麦（ＴｒｉｔｉｃｕｍａｅｓｔｉｖｕｍＬ．）合子与幼胚。应用金霉素（ＣＴＣ）和氟奋乃静（ＦＰＺ）荧光探针，观察了合子与胚胎发育过程中膜钙和活化钙调素的分布。合子原生质体ＣＴＣ荧光呈极性分布。二细胞至十几个细胞原胚时期各细胞间的ＣＴＣ和ＦＰＺ荧光均匀分布。幼小梨形胚胚体ＣＴＣ和ＦＰＺ荧光稍强于胚柄。接近分化的梨形胚ＣＴＣ荧光仅位于胚体与胚柄之间的几层细胞和胚体腹侧中部的几个细胞中。胚芽刚分化时，胚基部ＣＴＣ荧光较强，ＦＰＺ荧光则仅出现在胚基部。讨论了合子分离技术和膜钙与钙调素（ＣａＭ）在胚胎发育中的可能作用。

A method for calculation of ion distribution in reaction system forming hydroxide

A formula was proposed to calculate the distribution of metal ions quantitatively in chemical reaction system forming hydroxide where precipitation and complex are formed together. The effects of some factors on formation of precipitation and complex were investigated, and the corresponding precipitation rates of zinc, iron （III）, aluminum, copper and magnesium were calculated. As a result, it shows that the proposed formula is reliable. By the proposed formula, the existence state of metal ions in hydroxides reaction system with any metal ions can be well described and the effects of some factors on the distribution of metal ions were determined.

Spectral Differences of the Molecule-ion Adducts of β-Cyclodextrin and Lithium Carbonate

A small shielding effect on the hydrogen atoms of chiral carbons of β-cyclodextrin （β-CD） was detected by 1H nuclear magnetic resonance, but a large environmental change of the chiral carbon atoms at high concentration ratios of lithium carbonate （Li2CO3） to β-CD was observed by polarimetry in aqueous solution. These findings urged us to investigate whether different formation conditions of the molecule-ion system between Li2CO3 and β-CD in solid state were involved in different spectral performances. To answer the question, we prepared three adducts of Li2CO3 to β-CD, i.e., samples 1, 2, and 3, by magnetic stirring, solvothermal and grinding conditions, respectively. Powder X-ray diffraction and Fourier transformation infrared spectroscopy provided the information of formation of the three molecule-ion adducts. Besides, scanning electron microscope images provided different surface information of the three adducts. Further, significant spectral differences in thermal behavior of these adducts were found by thermogravimetry and derivative thermogravimetry.

Rare Earth Metals Ion-exchanged β-Zeolites as Supports of Platinum Catalysts for Hydroisomerization of n-Heptane

A series of Pt catalysts supported on the Hβ-zeolite that is ion-exchanged with the rare earth metal ions of Ce（III） and La（III）,are prepared by impregnation,characterized by inductively coupled plasma （ICP）,X-ray diffraction （XRD）,BET,temperature-programmed desorption of ammonia （NH3-TPD）,temperature-programmed reduction of hydrogen （H2-TPR） and H2-chemisorption techniques,and evaluated in the hydroisomerization of n-heptane with an atmospheric fixed-bed reactor.The reaction temperature,time on stream,space velocity,and the ratio of H2/n-heptane are changed to get the optimal conditions.The Ce（III） and La（III）-exchanged Hβ-zeolites exhibit higher selectivity for isomerized products than the neat Hβ-zeolite.Moreover,the Ce（III）-exchanged catalysts give higher conversions of n-heptane,whereas the La（III）-exchanged ones do not show any improvement in con-version.Under optimal conditions,the catalyst with 0.4% （by mass） Pt and 0.5% （by mass） Ce loading presents very high selectivity of isomerized products of 95.1% coupled with high n-heptane conversion of 68.7%.Effects of the ion-exchange of Ce（III） and La（III） on the catalytic performance are discussed in relation with the physico-chemical properties of catalysts.

Organotemplate-free Hydrothermal Synthesis of SUZ-4 Zeolite: Influence of Synthesis Conditions

Various conditions were investigated in detail for the novel organic template-free static hydrothermal synthesis of SUZ-4 zeolite in the presence of seeds. The obtained samples were characterized by XRD （X-ray diffraction）, SEM （scanning electron microscope）, TG （thermal gravimetric analysis）, ICP （inductively coupling plasma） elemental analysis, nitrogen sorption isotherm and surface area. The results show that pure SUZ-4 zeolites with high crystallinity are obtained in a broad window of synthesis conditions： seed mass concentration 0.2%-2%, SIO2/A1203 molar ratio 21 25, KOH/SiO2 molar ratio 0.33 0.43, H20/SiO2 molar ratio 7.14-38.1, aging time 24 h, crystallization temperature 160℃, and crystallization time 6-10 d. Also, crystallinity and size of the rod-like SUZ-4 zeolite crystals are found to alter with the conditions.

Theoretical research on vacuum separation of Au-Ag alloy

To provide an accurate prediction of the product component dependence of temperature and pressure in vacuum distillation and give convenient and efficient guidance for the designing of the process parameters of industrial production, according to the molecular interaction volume model(MIVM), the separation coefficient(β) and vapor-liquid equilibrium composition of Au-Ag alloy at different temperatures are calculated. Combined with the vapor-liquid equilibrium(VLE) theory, the VLE phase diagrams, including the temperature-composition(T-x) and pressure-composition(p-x) diagrams of Au-Ag alloy in vacuum distillation are plotted. The triple points and condensation temperatures of gold and silver vapors are calculated as well. The results show that the β decreases and the contents of gold in vapor phase increase with the distillation temperature increasing. Low pressures have positive effect on the separation of Ag and Au. The difference between the condensation temperatures of gold and silver is about 450 K in the pressure range of 1-10 Pa.

Probing Molecular Interactions in 1-Butyl-3-methylimidazolium Chloride-Water and 2,6-Dimethoxyphenol Mixtures Using Attenuated Total Reflection Infrared Spectroscopy

Molecular interactions of the ternary mixtures of 1-butyl-3-methylimidazolium chloride （[C4C1im]Cl）-water-2,6-dimethoxyphenol （2,6-DMP, a phenolic monomer lignin model compound） were investigated in comparison with the [C4C1im]Cl-water binary systems through attenuated total reflection infrared spectroscopy. Results indicated that the microstructures of water and [C4C1im]Cl changed with varying mole fraction of [C4C1im]Cl （xIL） from 0.01 to 1.0. This change was mainly attributed to the interactions of [C4C1im]Cl-water and the self-aggregation of [C4C1im]Cl through hydrogen bonding. The band shifts of C-H on imidazolium ring and the functional groups in 2,6-DMP indicated that the occurrence of intermolecular interactions by different mechanisms （i.e., hydrogen bonding or π-π stacking） resulted in 2,6-DMP dissolution. In the case of xIL=0.12, the slightly hydrogen-bonded water was fully destroyed and [C4C1im]Cl existed in the form of hydrated ion pairs. Interestingly, the maximum 2,6-DMP solubility （238.5 g/100 g） was achieved in this case. The interactions and microstructures of [C4C1im]Cl-water mixtures influenced the dissolution behavior of 2,6-DMP.

Upper Triangular Matrix of Lie Algebra and a New Discrete Integrable Coupling System

The upper triangular matrix of Lie algebra is used to construct integrable couplings of discrete solition equations. Correspondingly, a feasible way to construct integrable couplings is presented. A nonlinear lattice soliton equation spectral problem is obtained and leads to a novel hierarchy of the nonlinear lattice equation hierarchy. It indicates that the study of integrable couplings using upper triangular matrix of Lie algebra is an important step towards constructing integrable systems.

Enhancing Effect of Fe^(2+) on the Formaldehyde Production from Trimethylamine N-oxide Decomposition Catalyzed by the Extract of Harpadon nehereus Kidney

The effects of Fe2+ on the trimethylamine N-oxide (TMAO) demethylating activity of the Harpadon nehereus kidney extract were studied in this research.The activity of the kidney extract was presumably inhibited by ethylene diamine tetra-acetic acid (EDTA),which indicates that the kidney extract contains an enzyme or enzyme system with metal cations as activator.Activity of the kidney extract was enhanced significantly when Fe2+ was added into the model system in vitro.As the concentration of Fe2+ increased,the decomposing rate of TMAO increased rapidly until TMAO decomposed completely.The activity of the kidney extract was also enhanced by reductant such as ascorbic acid.Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) was employed to determine the content of total iron in a number of fishery products.Significant positive correlation between the contents of total iron and endogenous formaldehyde (FA) was found,especially in marine products.

Robust Scheme for Long-Distance Teleportation of an Unknown Atomic State

A scheme is presented for the long-distance teleportation of an unknown atomic state between two separated cavities. The scheme is based on the Raman coupling and cavity decay. In the scheme, the effective atom-cavity coupling strength is much smaller than the cavity decay rate and thus cavities of high quality factor are unnecesssary.

Molecular Simulation of CO2/H2 Mixture Separation in Metal-organic Frameworks： Effect of Catenation and Electrostatic Interactions

In this work grand canonical Monte Carlo simulations were performed to study gas separation in three pairs of isoreticular metal-organic frameworks (IRMOFs) with and without catenation at room temperature.Mixture composed of CO2 and H2 was selected as the model system to separate.The results show that CO2 selectivity in catenated MOFs with multi-porous frameworks is much higher than their non-catenated counterparts.The simulations also show that the electrostatic interactions are very important for the selectivity,and the contributions of different electrostatic interactions are different,depending on pore size,pressure and mixture composition.In fact,changing the electrostatic interactions can even qualitatively change the adsorption behavior.A general conclusion is that the electrostatic interactions between adsorbate molecules and the framework atoms play a dominant role at low pressures,and these interactions in catenated MOFs have much more pronounced effects than those in their non-catenated counterparts,while the electrostatic interactions between adsorbate molecules become evident with increasing pressure,and eventually dominant.

Isolation of Main Genes Involved in Flowering of Saffron （Crocus sativus L.） in Order to Study Effective Flowering Protein

Saffron （Crocus sativus L.） always is grown for using its flowers in nutrient industry, color industry and healthy compounds due to its flowers and specially stigmas. Because of its expensive flowers, surveying and recognizing on effective genes for flowering is very important and its results can help us to control rate and timing of flowering at an early stage of flowering. The gene and gene state meant Pistillata like MADS box （PIC2） were surveyed for recognizing its molecular mechanism. The molecular sequence at the genes has high similarity to members of family MADS that is a factor for controls of protein at flowering stage. PIC2 gene was studied by bioinforrnatics resources. Primers were designed for replicating the gene and DNA and RNA were extracted from saffron＇s leaves. The gene＇s eDNA was built by recopying enzyme and used such a pattern for replicating gene PIC2 at polymerase chain reactions （PCR）. Segments were replicated such 900 eDNA pair-nucleotides and a segment such 2,100 of DNA＇s pair-nucleotides. The gene codes a protein that was composed of 210 amino acids that has MADS sequence box. Analysis of protein＇s molecular structure and homological modeling of the protein indicated that it has a regular structure.

Application of NaHCO_3/ DTPA Extractant-ICP Spectrometry Technique in Soil Test for Availability of Nutrients and Heavy Metals

Soil test for availability of nutrients and heavy metals is extensively served as a means for the evaluations of soil fertility, and environmental effects and phytotoxicity of pollutants in soils, and for the fertilizer recommendation in agricultural and environmental sciences. Therefore, great attention has been paid to the measurement of elemental availability in soil test.

Design of Fe （Ⅲ） and Hg （Ⅱ） Ion Selective Electrodes

Principally the basis of ISE is selecting of a support solid matrix and a nonsoluble compound or complexes of insighted cation, mixed with this solid. For preparing the ISE membranes there are some materials such PVC, PE, organic polyelectrolytes, conducting polymers and inorganic compounds. The black white microscope photos are included, too. Detailed schemes and pictures of the electrodes and correlations were shown in the following article. Results are seen compatible for construction of the versatile ISE electrodes.

Construction of a chimeric hepatitis C virus replicon based on a strain isolated from a chronic hepatitis C patient

Subgenomic replicons of hepatitis C virus （HCV） have been widely used for studying HCV replication.Here,we report a new subgenomic replicon based on a strain isolated from a chronically infected patient.The coding sequence of HCV was recovered from a Chinese chronic hepatitis C patient displaying high serum HCV copy numbers.A consensus sequence designated as CCH strain was constructed based on the sequences of five clones and this was classified by sequence alignment as belonging to genotype 2a.The subgenomic replicon of CCH was replication-deficient in cell culture,due to dysfunctions in NS3 and NS5B.Various JFH1/CCH chimeric replicons were constructed,and specific mutations were introduced.The introduction of mutations could partially restore the replication of chimeric replicons.A replication-competent chimeric construct was finally obtained by the introduction of NS3 from JFH1 into the backbone of the CCH strain.

Chemical Composition and Mechanical Characteristic of Nitrogen Ion Beam Mixed Carbon Nanolayer

Ion beam methods for modification of nanohardness of surface nanolayers of the titanium alloy Ti6AI4V were applied. After deposition of carbon nanolayers by electron beam evaporation, the ion implantation of nitrogen into samples was carried out. The chemical composition of the modified surface area was investigated by AES （auger electron spectroscopy）. The nanohardness of resulted ion beam modified surface nanolayers were investigated by nanoindentation testing. The measured concentration profiles indicate the atomic mixing of carbon into the substrate. It was found that the modified samples had a markedly higher nanohardness than the unmodified samples. The increased nanohardness is attributed to the newly created phases in the surface area.

Aromaticity of Heterofullerenes C18BxNy （x＋y=2） and Their Molecular lons

The aromaticity of all possible substituted fullerene isomers of C18N2, C18B2, C18BN, and their molecular ions which originate from the C20 （Ih） cage were studied by the topological resonance energy （TRE） and the percentage topological resonance energy methods. The relationship between the aromaticity of C18BxNy isomers and the sites where the heteroatoms dope at the C20 （Ih） cage is discussed. Calculation results show that at the neutral and cationic states all the isomers are predicted to be antiaromatic with negative TREs, but their polyvalent anions are predicted to be aromatic with positive TREs. The most stable isomer is formed by heteroatom doping at the 1,11-sites in C18N2. C18B2, and C18BN. Heterofullerenes are more aromatic than C20. The stability order in the neutral states is C18N2〉C18BN〉C18B2〉C20. The stability order in closed-shell is C18B2^8- 〉C20^6- 〉C18BN^6- 〉C18N2^4-. This predicts theoretically that their polyvalent anions have high aromaticity.

Mineral Constituents in Common Chanterelles and Soils Collected from a High Mountain and Lowland Sites in Poland

This paper reported the results of the determination of Ag, A1, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, Rb, Sr and Zn in Common Chanterelles （Cantharellus cibarius） Fr. and surface soil layer （o-io cm） underneath the fruiting bodies. Mushrooms and soils were collected from a lowland site in the Hel Peninsula （Baltic Sea coast） and a high mountain site in the Tatra Mountains. The trace elements were determined using validated method and inductively coupled plasma - atomic emission spectroscopy （ICP-AES）. Common Chanterelles that emerged at sites poor in mineral nutrients podzols of the Hel Peninsula forests efficiently bioeoncentrated several essential trace elements （K, P, Co, Cu, Mn, Na, Zn）, while the abundance of those elements in carpophores was around half less compared to specimens from Zakopane region and which emerged in soils much richer in minerals. Common Chanterelles collected at two spatially distant background areas in Poland were only weakly contaminated with metals such as Ag, Cd, Hg and Pb. The maximum tolerable Cd and Pb contents of certain cultivated mushrooms are regulated in the European Union by law and these hazardous metals in C. cibarius were far below tolerance limits set.

Preparation and adsorption behaviors of Cu(Ⅱ) ion-imprinted polymers

Imprinted polymers were prepared for selective removal of Cu（Ⅱ） ions from metal solutions. Three ion-imprinted polymers were synthesized with methacrylic acid （MAA）, acrylamide （AA） and N,N＇-methylenebisacrylamide （MBAA） respectively as the functional monomers, ethleneglycoldimethacrylate （EGDMA） as the cross-linking agent, 2,2＇- azobisisobutyronitrile （AIBN） as the initiator and Cu （Ⅱ） ion as the imprint ion. The template Cu （Ⅱ） ion was removed from the polymer by leaching with a liquid of a 1：1 volumetric ratio of HCl to ethylenediaminetetraacetic acid （EDTA）. The capacity and selectivity of Cu（Ⅱ） ion adsorption were investigated with the three imprinted polymers and their non-imprinted counterparts. The polymers have a maximum adsorption capacity at pH 7.0. The isotherm of their batch adsorption of Cu（Ⅱ） ions shows a Langmuir adsorption pattern. Imprinted polymers all have a much higher capacity and higher selectivity of Cu（Ⅱ） adsorption than nonimprinted ones. MAA polymer benefits the most from imprinting. Imprinted MAA polymer has the highest selectivity when used to rebind Cu （Ⅱ） ion from an aqueous solution in the presence of other metal ions. Ion imprinting can be a promising technique of preparing selective adsorbents to separate and preconcentrate metal in a medium of multiple competitive metal ions through solid phase extraction （SPE）.

Selective recovery of Cu(Ⅱ) through polymer inclusion membranes mediated with 2-aminomethylpyridine derivatives

The Cu(Ⅱ) separation behaviors with polymer inclusion membranes(PIMs) are explored by modifying 2-aminomethylpyridine derivatives with hydrophobic alkyl chains, including 2-[N-(tert-butyloxycarbonylmethyl)-2-picolyamino]acetate(AMB), N,N-dioctyl-2-aminomethylpyridine(AMD), tert-butyl 2-(N-octyl-2-picolyamino) acetate(AMC), and N,N-didecyl-2-aminomethylpyridine(AME). The transport flux and selectivity of Cu(Ⅱ) are determined by optimizing composition and structure of carriers and plasticizers. The results show that the hydrophobic modification of 2-aminomethylpyridine derivatives can boost the selective transport of copper ions in PIMs and membrane stability. In the optimum composition of 30 wt.% PVC, 30 wt.% AME, and 40 wt.% NPOE, the initial flux of Cu(Ⅱ) is 5.8×10^(−6) mol·m^(−2)·s^(−1). The FT-IR and XPS spectra identify that the alkyl amine functional groups of AME involve in the transport of copper chloride species. The SAXS analysis demonstrates that the generated micro-channels in PIMs induced by the hydrophobic modification of 2-aminomethylpyridine derivatives can contribute to the enhanced Cu(Ⅱ) flux.