991 resultados para Brunelleschi, Filippo, 1377-1446.


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IEECAS SKLLQG

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Equilibration and equilibration rates have been measured by colliding Sn nuclei with different isospin asymmetries at beam energies of E/A = 35 MeV. Using the yields of mirror nuclei of Li-7 and Be-7, we have studied the diffusion of isospin asymmetry by combining data from asymmetric Sn-112 + Sn-124 and Sn-124 + Sn-112 collisions with those from symmetric Sn-112 + Sn-112 and Sn-124 + Sn-124 collisions. We use these measurements to probe isospin equilibration in central collisions where nucleon-nucleon collisions are strongly blocked by the Pauli exclusion principle. The results are consistent with transport theoretical calculations that predict a degree of transparency in these collisions, but inconsistent with the emission of intermediate mass fragments by a single chemically equilibrated source. Comparisons with quantum molecular dynamics calculations are consistent with results obtained at higher incident energies that provide constraints on the density dependence of the symmetry energy.

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详细阐述了基因工程微生物(GEM)在环境释放中需考虑的主要问题:GEM的构建、基因转移、适合度、扩散、转运和潜在的生态影响等,并针对GEM特定的生态学特征和生态影响,提出了基因工程微生物生态学研究宜采取“具体问题具体分析”的策略,制定相应的研究方案,为安全有效地在非受控条件下应用GEM铺平道路。

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Heterogeneous electrocatalytic reduction of hydrogen peroxide (H2O2) by C-60 is reported for the first time. C-60 is embedded in tetra octyl ammonium bromide (TOAB) film and is characterized by scanning electron microscopy and cyclic voltammetry. Electrocatalytic studies show that the trianion of C-60 mediates the electrocatalytic reduction of H2O2 in aqueous solution containing 0.1 M KCl. Application of such film modified electrode as an amperometric sensor for H2O2 determination is also examined.

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合成了一系列齐聚苯胺修饰的三联吡啶铁配合物,研究了齐聚苯胺链长、不同取代基等对配合物光谱性质和氧化还原性质的影响。结果表明,相对于配合物[Fe(TPY)2]2+(TPY:三联吡啶),供电子齐聚苯胺单元的引入,使得修饰基团与配合物中心核[Fe(TPY)2]2+之间形成了强的D-A体系,导致配合物1MLCT吸收波长显著红移至594 nm,且摩尔吸光系数增加近5倍。配合物同时具有基于金属中心、三联吡啶配体和齐聚苯胺单元的多个氧化还原过程,强拉电子取代基使齐聚苯胺单元氧化还原峰简并且峰电势明显正移,而正丁基取代基对氧化还原峰电势的影响较小。

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Cyclic oligomers of phenolphthalein polyarylene ether sulfone(ketone) were prepared through cyclo-depolymerisation of corresponding polymers using CsF as the catalyst in dipolar aprotic solvent DMAc and DMF, and a family of macrocycles containing from dimer up to at least heptamer were confirmed. by GPC, HPLC and MALDI-TOF-MS. The yields of cyclics get as high as 86.3% and 87.9% respectively.

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In the presence of F-, OH-, Cl-, electrochemical redox of (OEP)Mg(II) [2,3, 7,8,12,13,17,18 octaethyl-21H, 23H-porphine magnesium (II)] are investigated in DCE/0.1 mol/L solution by cyclic voltammetry and spectroelectrochemistry, In the presence of anions, anions are axially coordinated to (OEP)Mg(II) generate (OEP)Mg(II)Y, the E-1/2 of (OEP)MS(II)Y oxidation are negatively shifted. A chemical reaction following the second oxidation step is observed, the E-1/2 of the reaction product is obtained. Mechanism of (OEP)Mg(II) in the halogen and OH- anions titration process has been proposed.

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Conductive polyaniline was found to have special marine antifouling property. The coating from conducting polyaniline and epoxy resin(or polyurethane) can last 6-9 months in Southern China sea, i.e., less than 10% of the coating surface was fouled during this period. The conducting polyaniline has special synergetic antifouling effect on other antifouling agents like cuprous oxide or 4, 4'-dichlorodiphenyltrichloroethane. The conductivity of the polyaniline was found to be extremely important for its antifouling effect. Moreover, employing aliphatic polyamine as solvent of emeraldine base and curing agent of epoxy resin, a new technique to process corrosion prevention coating containing emeraldine base was developed, therefrom the emeraldine base and epoxy resin was in molecular level blending. This technique was solvent free and extremely effective, i.e., only 1wt% of emeraldine base in the coating can have good corrosion prevention property.

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用电化学滴定和现场光谱电化学方法研究考察了DCE中OH~-,F~-和Cl-等阴离子存在下的(OEP)Mg(Ⅱ)的电极氧化过程.发现阴离子能与(OEP)Mg(目)轴向配位,形成五配位化合物,从而引起(OEP)Mg(Ⅱ)的氧化峰电位的负移;在生成二价环阳离子的过程中伴随后行化学反应.获得了反应产物的氧化还原峰电位.