58 resultados para 783


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National Natural Science Foundation of China [40471134]; program of Lights of the West China by the Chinese Academy of Science

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目的考察山茱萸与五味子配伍前后两药主要组分的含量变化规律。方法利用高效液相色谱(HPLC)方法,比较了配伍前后单煎液、合煎液和单煎合并液中两药主要组分马钱苷、没食子酸和五味子醇甲的含量变化。结果在配伍比例较低(≤4:4)时,五味子促进了山茱萸中马钱苷的溶出。合煎液中的没食子酸、五味子醇甲组分的百分含量随着五味子配伍比例的增大呈线性减小,且均低于单煎液。单煎合并液中这3种组分的含量均高于同比例合煎液。结论山茱萸五味子配伍对两药主要组分溶出有较大影响,该影响主要在煎煮过程中发生。

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A general and facile ultrasonic irradiation method has been established for the synthesis of the lanthanide orthovanadate LnVO(4) (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) nanoparticles from an aqueous solution of Ln(NO3)(3) and NH4VO3 without any surfactant or template. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), and photoluminescence (PL) spectra as well as kinetic decays were employed to characterize the as-prepared products. Ultrasonic irradiation has a strong effect on the morphology of the LnVO(4) nanoparticles. The SEM and TEEM images illustrate that the as-formed LnVO(4) particles have a spindle-like shape with an equatorial diameter of 30-70 nm and a length of 100-200 am, which are the aggregates of even.

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Gly-Gly-His tripeptide modified microcantilever was developed by carbodiimide attachment of the Gly-Gly-His tripeptide onto a 3-mercaptopropionic acid(MPA) modified gold surface. The interaction of peptide with Cu2+ ion was studied. At a relative high concentration of Cu2+, the cantilever bent toward the gold side initially as the N atom of imidazole ring and carboxyl group in different peptide coordinate with Cu2+, which results in a tensile surface stress. And then the reversed deflection of microcantilever was observed, which implies that the peptide-Cu2+ complex are formed with conformation transition. In another case, i.e., at a relative low concentration Of Cu2+, only the process of conformation transition was observed due to the coordination mode can not be formed initially. The influences of pH and salt concentration of the test solution on the performance of the sensor were studied. The results show that the maximum deflection was obtained at pH 7 and the bonding Of Cu2+ to the Gly-Gly-His tripeptide was inhibited due to the formation Of CuClx2-x.

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将三肽Gly-Gly-His(GGH)共价键合到MPA修饰的微悬臂梁表面,研究了肽与Cu2+的相互作用过程。研究发现,在Cu2+浓度较高时,Cu2+能快速与不同肽链上的羧基和咪唑环配位,并通过连锁反应诱导悬臂梁向镀金面偏转;而后肽链上的氮原子与Cu2+配位,同时构象发生变化,由直链转变成折叠状,进而增加链间的作用力使悬臂梁反向偏转;而Cu2+浓度低时不能实现连锁反应诱导悬臂梁表面快速的形成向内的拉力,直接通过构象变化推动悬臂梁反向偏转。考察了溶液pH值、Cl-浓度对GGH与Cu2+作用的影响,结果表明,在pH7.0的条件下GGH与Cu2+作用导致悬臂梁偏转最大。Cl-的存在会与Cu2+形成CuCl2x?x配合物不易与肽链结合。

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Sequential extraction procedures were widely applied for speciation of radioactive elements. In this study, the sequential extraction procedure developed by Martinez-Aguirre was employed for quantification of different chemical forms of thorium in the soil. The total amount of thorium in contaminated soil was much higher by four-fold than the local background value. The soil properties affect the amount of thoriurn and distribution of fractions in contaminated soil. Results showed that the proportion of thorium in soils from Baotou was found as the residual fraction (F5 + F6) > absorbed fraction (F3), coprecipitated fraction (F4) > carbonates fraction (172) and exchangeable fraction (F1) that could be available to plants. The recovery, calculated by ratio of the sum of the six fractions to the pseudo-total content of thorium, was in the range from 96% to 110%. A comparison was carried out between the sequential extraction and the single extraction to evaluate the selectivity of the extractants. It was found that the amount of thorium of absorbed fraction (H) was higher in the single extraction than that estimated in the sequential extraction, possibly duo to transform of the labile form. While for non-residual fraction analysis, the single extraction scheme was a desirable alternative to the sequential extraction procedure.

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The electrolyte, NaBF4, can be enriched into the matrix of poly(3,4-ethylenedioxythiophene) (PEDOT) film during the p-doping potential cycling between 0.6 and -0.9 V. It has been demonstrated that this enrichment is originated from the mixed ion transfer between doping and dedoping, i.e. BF4- anion migrate into the PEDOT film during the oxidation process, the Ne cation insert into the film during the reduction process, and then, the electrolyte is accumulated into the film matrix after the multiple CV cycling. The quantitative analysis of energy-dispersive X-ray spectroscopy (EDX) confirmed the enrichment of NaBF4 in the PEDOT film.

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用DSC研究了HDPE与MMT负载的催化剂熔融共混和原位聚合得到的两种纳米复合材料的熔融、结晶行为和等温结晶动力学.结果表明,HDPE与熔融共混样品的结晶度、平衡熔点、球晶生长速率和结晶能力大体相同;原位聚合得到的HDPE/MMT纳米复合材料的结晶度和平衡熔点高于纯HDPE;在相同过冷度条件下熔融结晶速率和结晶能力低于纯HDPE,而在相同结晶温度Tc下,熔融结晶速率和结晶能力则高于纯HDPE.纯HDPE的晶体生长侧向单位面积表面自由能最小,其次是熔融共混样品,原位聚合样品最大,且随MMT含量的增加逐渐升高.

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It was demonstrated feasible that underpotential deposition(UPD) of copper on a monolayer-modified gold substrate can be used to determine the gold electrode area. The deposition and stripping of a Cu adlayer can take Place reversibly and stably at a bared or a self-assembled monolayer modified gold electrode. The growth kinetics of decanethiol/Au was also investigated via Cu UPD. The difference between the assembling kinetics determined by UPD and that by quartz crystal microbalance measurements reveals the configuration transmutation of the assembled molecules from a disordered arrangement to an ordered arrangement during the self-assembling processes.

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本文报道了SrAl2 B2 O7:Dy3+、BaAl2 B2 O7:Dy3+、SrAl3BO7:Dy3+、La2 CaB10 O19:Dy3+的紫外-真空紫外 (UV—VUV)激发光谱和UV激发下的发射光谱。根据发射光谱讨论了Dy3+离子在这几种基质中发光的黄蓝比 (Y/B)。在VUV激发光谱中推测了Dy3+的f-d跃迁及电荷迁移态(CTS)和基质吸收的位置

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Poly-o-methylaniline (poly-o-toluidine) was doped by some protonic acids. It was found that the acidity, molecular size and oxidizing ability of protonic acids affected the doping level and conductivity of polymer obtained to some extent. The organic acid

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采用不同种类质子酸对聚邻甲苯胺进行掺杂,发现质子酸的酸性、分子尺寸和氧化性均不同程度地影响其掺杂率和电导率.大分子尺寸有机强酸掺杂可诱导掺杂态聚合物的溶解性.ESR测量结果表明,中性聚邻甲苯胺的自旋电子主要定域在杂原子上;质子酸掺杂导致氮原子上的电子产生重新组态,并部分离城到邻近的芳环上,显示出芳香π-电子的特性.电阻与压力依赖性研究揭示出质子酸掺杂聚邻甲苯胺的导电类型为电子型.

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The thermal stability and the solid solid phase transitions in Ills compounds with n = 7-12 have been studied by DSC and TG methods. Comparision with CnZn compounds want made. The nature of three phases of CnCu has been discussed in terms of infrared spectroscopy and the assignment of the phase transitions has been given. The thermal stability of CnCu is lower than that of CnZn and presents an obvious odd even effect. All of these compounds exhibit two solid solid phase transitions in the temperature range of 248-337 K. The peak tempe nature of phase transitions changes regularly. The peak temperature or the main phase transition increases with the chain length. The total transition enthalpies and entropies increase with increasing chain length. When n <= 9, the high temperature phase exists in a partial disorder state. When n >= 10, the high temperature phase exists in a conformational disorder state. The main phase transition and the phase transition at 307.7 K of CnCu may mainly are from the change of the packing structure and the change of the partial conformational order-disorder of alkyl chain, respectively.