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171.
The present study contains the analyses performed for pigment samples taken from the Princely church of Curtea de Arges, one of the oldest churches in Romania. The results of our investigations have shown the source of these samples, thus being identified the pigments: natural ultramarine, cinnabar, red earth, and calcium carbonate in the painting from the 14th century, the pigments: lead white, zinc white, and Prussian blue in the repainting from the 19th century and the pigments zinc white, titanium dioxide white, bone white, yellow ochre, red ochre, green earth, artificial ultramarine, and mars red in the interventions carried out in the 20th century. The analyses consisted of light microscopy (LM) and microchemical tests, as well as energy dispersive X-ray (EDX) analysis. This system of analyses allows one to precisely determine the authenticity of certain pigments, thus avoiding the dating errors for different interventions carried out on the original mural painting from the Saint Nicholas Princely church of Curtea de Arges. 相似文献
172.
The complete infrared and Raman spectra of 1,1-difluoro-1-silacyclopentane and 1,1-dichloro-1-silacyclopentane have been recorded and analyzed. Furthermore, a number of the vibrational frequencies of the silacyclopentane and silacyclopentane-1, 1-d2 molecules have been reassigned.A normal coordinate calculation for each of these molecules was carried out and this demonstrated the validity of the assignments. Considerable mixing of the modes was found especially where ring vibrations and SiX2 motions were involved. 相似文献
173.
Roman Pogreb Oleg Popov Vlad Lirtsman Oleg Pyshkin Alexander Kazachkov Albina Musin Gene Whyman Binyamin Finkelshtein Yuri Shmukler Dan Davidov Alexander Gladkikh Edward Bormashenko 《先进技术聚合物》2006,17(1):20-25
The work is devoted to luminescent properties of trivalent lanthanide complexes dispersed in thermoplastic host matrices. Polyethylene films and polypropylene‐rods, both doped with these complexes, were manufactured using an extrusion technique. Two kinds of dopants were used: Eu(III)‐thenoyltrifluoroacetone‐1,10‐phenanthroline complex (1) and Eu(III)‐La(III)‐1,10‐phenanthroline complex (2). Absorption, excitation, emission spectra and lifetime of luminescence were studied. The impact of the polymer matrix on the emission spectra was investigated. Emission spectra of the films were studied at room and helium temperatures. Time‐of‐flight secondary ion mass spectrometry (TOF‐SIMS) surface mapping showed that in the Eu(III)‐La(III) complex europium forms islands (clusters) with a dimension of 1 µm, whereas lanthanum was dispersed more uniformly in the polymer matrix. Dependence of emission intensity on the excitation was determined. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
174.
175.
Nb 掺杂LiFePO4/C 的一步固相合成及电化学性能 总被引:1,自引:0,他引:1
用固相法一步合成了Nb掺杂的LiFePO4/C复合材料, 研究了Nb掺杂量对材料电化学性能的影响. 结果表明, Nb掺杂后LiFePO4/C复合材料的电化学性能明显提高. 在0.5C、1C和2C充放电倍率下, 名义成分为Li0.96Nb0.008FePO4/C正极材料的比容量分别为161、148和132 mAh•g−1, 已达到实用化水平. 阻抗谱和循环伏安特性测试显示, Nb掺杂有效地降低了复合材料电极的阻抗和极化, 说明Nb掺杂的主要作用是提高了LiFePO4的电子电导率. 相似文献
176.
The attempt to prepare structurally well-defined polymer/inorganic composite particles, i.e., poly(methyl methacrylate) (PMMA)/CaCO3/SiO2 three-component composite particles, via reverse atom transfer radical polymerization (ATRP), using 2-2′-azo-bis-isobutyronitrile as initiator and Cu(II) bromide as catalyst was reported. CaCO3/SiO2 two-component composite particles were first obtained through sol–gel method, and their morphology and surface element information were determined by transmission electron microscopy and X-ray photoelectron spectroscopy, respectively. The results indicate that the CaCO3 was encapsulated by the obtained SiO2. After being modified by silane coupling agent, the CaCO3/SiO2 composite particles copolymerized with methyl methacrylate (MMA) under standard reverse ATRP conditions to produce PMMA/CaCO3/SiO2 three-component composite particles. In the case concerned, first-order kinetic plots and linear increase of molecular weight (Mn) vs conversion and narrow molecular weight distribution for the graft polymer samples were observed. Furthermore, the gel permeation chromatography results illustrated that both the free PMMA chains from the solvent and the graft PMMA chains from the surface of CaCO3/SiO2 two-component composite particles were growing at the same rate. Characterizations of the PMMA-grafted CaCO3/SiO2 composite particles were done by Fourier transform infrared and thermogravimetric analysis. The results showed that the surface of the modified inorganic particles was grafted by the MMA and that the grafting percentage was about 8.7%. 相似文献
177.
Many studies have focused on effective ways to exploit enzyme immobilization on an electrode surface to help improve the performance of enzymatic electrochemical biosensors. Herein, a novel glucose sensor was fabricated by immobilizing glucose oxidase (GOx) onruthenium-based conjugated polymer (CP) and metal-organic framework (MOF) nanocomposites. This has not only reduced the applied potential to 0.2 V (vs. Ag/AgCl), but also improved the effective surface area for enzyme immobilization.PPG@Ru@UiO-66-NH2 was tailored by controlled chemical synthesis from a pre-synthesized water-soluble conjugated polymer (poly(N-phenylglycine)) and metal-organic framework (UiO-66-NH2). The resulting nanocomposites were characterized using Fourier transform infrared spectroscopy, X-ray fluorescence, scanning electron microscopy, and cyclic voltammetry. The PPG@Ru@UiO-66-NH2/GOx coated electrodedisplayed a linear measurementrange for glucose from 1 mM to 10 mM, with a sensitivity of 45.92 μA ⋅ mM−1cm−1 and limit of detection of5 μM( ). Furthermore, the practical application of the fabricatedglucosesensor was tested in simulative blood samples with satisfactoryaccuracy. This approach alsoopens a new door for applications regarding both enzymatic electrochemical biosensors and enzymatic biofuel cells (EBFCs). 相似文献
178.
Alfonso Loaiza Dan Borchardt Francisco Zaera 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》1997,53(14):2481-2493
13C NMR at 125.76 MHz with 1H and 2H decoupling, 2H NMR at 76.77 MHz with 1H decoupling, and 1H NMR at 500.14 MHz with 2H decoupling were employed as analytical tools to study the complex mixtures of deuterated ethanes resulting from the catalytic H–D exchange of normal ethane with gas-phase deuterium in the presence of a platinum foil. Reference samples consisting of 1:1 binary mixtures of pure normal ethane and ethane-dn (n=1–6) were used to identify the peak positions in the 13C, 2H, and 1H NMR spectra due to each individual isotopomer, and the effect of isotopic substitution on the chemical shifts was determined in each case. While the NMR of all three nuclei worked well for the identification of the individual components of the 1:1 standard mixtures, both 1H and 2H NMR suffered from inadequate resolution when studying complex reaction mixtures because of the broadening of the lines due to 1H–1H (1H NMR) and 2H–2H (2H NMR) couplings. 13C NMR was therefore determined to be the method of choice for the quantitative analysis of the reaction mixtures. Using the 13C NMR results, a correlation that takes into account the primary and secondary isotope substitution effects on chemical shifts was deduced. This equation was used for the identification of the individual components of the mixtures, and integration of the individual observed resonances was then employed for quantification of their composition. This study shows that 13C NMR with 1H and 2H decoupling is a viable procedure for studying mixtures of deuterated ethanes. Furthermore, the additivity of the isotopic effects on chemical shifts and the transferability of the values obtained with ethane to other molecules makes this approach general for the analysis of other isotopomer mixtures. 相似文献
179.
γ-Fe2O3纳米粉的低热固相制备及其电磁损耗特性(英) 总被引:6,自引:0,他引:6
The Fe(OH)3 precursor was prepared by solid -state reaction with Fe(NO3)3·9H2O, NaOH and dispersed poly-ethylene glycol at low heating temperature(25 ℃). Synthesis of iron oxide (γ-Fe2O3) nanoparticle was achieved by thermal decomposition of Fe(OH)3·xH2O precursor. The nanoparticle was characterized by TG-DTA, X-ray diffra-ction, TEM etc. The results showed that the nanoparticle was composed of γ-Fe2O3 and was a better absorber for electromagnetic wave within the low frequency band. 相似文献
180.
Aminopyrene functionalized mesoporous silica for the selective determination of resorcinol 总被引:1,自引:0,他引:1
Aminopyrene was convalently anchored onto the surface of mesoporous MCM-41 silica by post-grafting. This organic-inorganic hybrid has been applied as sensing material to phenols determination. Experimental results reveal that the functionalized material presents good sensitivity and selectivity towards resorcinol and can be used for resorcinol determination in water at pH 6.0. The fluorescence intensity of aminopyrene functionalized mesoporous silica decreases proportionally to the logarithm of resorcinol concentration in water. The linear range for resorcinol detection lies in 4.79-163 μM with a detection limit of 2.86 μM (S/N = 3). 相似文献