969 resultados para Variables 0 - 1


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A surface-renewable tris (1,10-phenanthroline-5, 6-dione) iron (II) hexafluorophosphate (FePD) modified carbon ceramic electrode was constructed by dispersing FePD and graphite powder in methyltrimethoxysilane (MTMOS) based gels. The FePD-modified electrode presented pH dependent voltammetric behavior, and its peak currents were diffusion-controlled in 0.1 mol/L Na2SO4 + H2SO4 solution (pH = 0. 4). In the, presence of iodate, clear electrocatalytic reduction waves were observed and thus the chemically modified electrode was used as an amperometric sensor for iodate in common salt. The linear range, sensitivity, detection limit and response time of the iodate sensor were 5 x 10(-6)-1 x 10(-2) mol/L, 7.448 muA.L/mmol, 1.2 x 10(-6) mol/L and 5 s, respectively. A distinct advantage of this sensor is its good reproducibility of surface-renewal by simple mechanical polishing.

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H-1 NMR spectroscopy has been used to assess long-term toxicological effects of a rare earth. Male Wistar rats were administrated orally with La(NO3)(3) at doses of 0.1, 0.2, 2.0, 10, and 20 mg/kg body wt, resp., for 3-6 months. Urine was collected at 1, 2, and 3 months and serum samples were taken after 6 months. Numerous low-M-r metabolites in rats serum and rats urine, including creatinine, citrate, glucose, ketone bodies, trimethylamine N-oxide (TMAO), and various amino acids, were identified on 400- and 500-MHz H-1 NMR spectra. La3+-induced renal and liver damage is characterized by an increase in the amounts of the excreted ketone bodies, amino acids, lactate, ethanol, succinate, TMAO, dimethylamine, and taurine and a decrease in citrate, glucose, urea, and allantoin. Information on the molecular basis of the long-term toxicity of La(NO3)(3) was derived from the abnormal patterns of metabolite excretions. An assay of some biochemical indexes and analysis of some enzymes in plasma supported NMR results.

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Nine triphenyltin - 2 - (1,2 - ethylenedithio) methylene - 3 - oxo - 5 - aryl - 4 - pentenicates were synthesized. The crystal structure of the title compound 3b (C33H28O3S2Sn) was determined by X - ray diffraction analysis. The crystal belongs to triclinic system, space group P(1)overbar with a = 0.9074 (2) nm, b = 1.6809(3)nm, c = 2.1834(4)nm, alpha =77.57(3)degrees, beta = 88.04(3)degrees, gamma = 89.47(3)degrees, V = 3.2503nm(3), Z = 2, R = 0.0592. In crystal of 3b, there exist intramolecular 0-Sn coordination bonds, with carboxylate group acting as a bidentate ligand: Sn(1)-0(1) = 0.2086(5) and Sn(1)-0(2) = 0.2594nm, having a deformed trigonal bipyramidal geometry.

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A novel morphology of TPBD crystals consisting of a three-dimensional interlaced network was obtained by casting the self-seeded 0.1% benzene solution onto carbon-boated mica. Both the transmission electron microscopy (TEM) and electron diffraction (ED) analyses showed that the network was composed of well-developed lamellae. It is imagined this interesting morphology is the results of asymmetrical growth of the original TPBD lamellae on the amorphous interface, and that their preferred orientation changed when they encountered each other.

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利用循环伏安法研究了玻璃微米 /纳米管支持的水 / 1 ,2 -二氯乙烷 ( DCE)界面上邻菲咯啉加速质子的转移过程 .将装有水溶液的微米 /纳米管插入到 DCE溶液中 ,可以形成微米 /纳米级 -液 /液界面 ,在选定的实验条件下 ,其作用类似于微米 /纳米电极 .用微米管考察了此加速转移过程的半波电位与 p H值 ( 1 .1~7.5 )的关系 ,利用 Matsuda等提出的理论公式计算了邻菲咯啉与质子在有机相和水相中的络合常数比 .并用纳米管计算得到邻菲咯啉加速质子在水 / DCE界面转移过程中的标准速率常数 ( k0 )和转移系数 (α)分别为( 0 .1 83± 0 .0 5 4 ) cm/ s和 0 .70± 0 .0

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The chemical bond parameters, that is, bond covalency, bond susceptibility, and macroscopic linear susceptibility of La1-xCaxCrO3 (x = 0.0, 0.1, 0.2, 0.3) has been calculated using a semiempirical method. This method is the generalization of the dielectric description theory proposed by Phillips, Van Vechten, Levine, and Tanaka (PVLT). In the calculation of bond valence, two schemes were adopted. One is the bond valence sums (BVS) scheme, and the other is the equal-valence scheme. Both schemes suggest that for the title compounds bond covalency and bond susceptibility are mainly influenced by bond valence and are insensitive to the Ca doping level or structural change. Larger bond valences usually result in higher bond covalency and bond susceptibility. The macroscopic linear susceptibility increases (only slightly for BVS scheme) with the increasing Ca doping level. (C) 1999 John Wiley & Sons, Inc.

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Five different molecular weight phenolphthalein poly(aryl ether ketone) (PEK-C) fractions in CHCl3 were studied by static and dynamic laser light scattering(LLS). The dynamic LLS revealed that the PEK-C samples contain some large polymer clusters. These large clusters can be removed by filtering the solution with a 0.1-mu m filter. We found that the persistence length of PEK-C in CHCl3 at 25 degrees C is similar to 2 nm and the Flory characteristic ratio, C-infinity is similar to 25. Our results showed that [R(g)(2)](1/2)(z) = (3.50+/-0.20) x 10(-2)M(w)(0.54+/-0.01) and [D] = (2.37+/-0.05) x 10(-4)M(w)(-0.55+/-0.01), with [R(g)(2)](1/2)(z), M(w), and [D] being the z-average radius of gyration, the weight-average molecular weight, and the z-average translational diffusion coefficient, respectively. A combination of static and dynamic LLS results enabled us to determine D = (2.20+/-0.10) x 10(-4)M(-0.555+/-0.015), where D and M correspond to monodisperse species. Using this calibration between D and M,we have determined molecular weight distributions of five PEK-C fractions from their corresponding translational diffusion coefficient distribution.

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The type of oxygen species in perovskite-type oxides LaMnyCo1-yO3 (y = 0.0, 0.1, 0.3, 0.5, 0.7, 0.9, 1.0) has been studied by means of XRD, XPS and TPD. The catalytic activity in ammonia oxidation was also investigated. It was found that there were three desorption peaks in TPD curve corresponding to three types of oxygen species (alpha, beta, beta'). The desorption temperatures were 293 K less-than-or-equal-to T(alpha) less-than-or-equal-to 773 K, 773 K less-than-or-equal-to T(beta) less-than-or-equal-to K and T(beta') greater-than-or-equal-to 1073 K respectively. The relationship among the composition, structure and the catalytic property of.the catalyst was correlated and could be explainned with a model based on solid defect reaction and the interaction between Co and Mn ions. The adsorption strength and quantity of a oxygen are proportional to the catalytic activity. The, result indicates that the synergetic effect between B-site ions seems to the benefit of the ammonis oxidation reaction.

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本文介绍自行合成的LaxBa_(1-x)SnO_3(x=00.2)的结构、电学性质、温敏性质和气敏性质,其结构均为立方晶体,晶胞参数随镧含量的增加而减少.La_(0.1)Ba_(0.9)SnO_3在室温至600℃温区内,电阻随温度升高而线性下降,有可能用作温敏元件.当La_(0.1)Ba_(0.9)SnO_3作成旁热式气敏元件时,有可能用于(1010000)10~(-6)乙醇蒸汽的检测,而不受煤气、液化汽、汽油和烟的干扰.

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采用蒸发溶液法从磷酸溶液中生长出一系列Ce_xGd_yTb_(1-x-y)P_5O_(14)晶体.测定了它们的结构.它们属于单斜晶系,空间群P2_(1/c).测定了Ce_(0.9)Gd_(0.1)P_5O_(14)、Ce_(0.9)Tb_(0.1)P_5O_(14)和La_(0.8)Gd_(0.1)Tb_(0.1)P_5O_(14)等晶体的光谱.首次观察到,将Gd加入Ce_xTb_(1-x)P_5O_(14)晶体中形成.Ce_xGd_yTb_(1-x-y)P_5O_(14)时阻碍了Ce~(3+)→Tb~(3+)的能量传递,导致Ce~(3+)的发射峰增强,Tb~(3+)的~5D_4—~F_J发射峰减弱、而~5D_3—~7F_J发射峰增强.

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杂多酸是种类多,应用广的重要的无机化合物。其中有一类是12-系列化合物Z,(XM_(12-n)M_n′O_(40))·mH_2O,中心离子X可以是过渡元素或非过渡元素;M常是Mo、W;M′为V_(5+)、Mn_(2+)、CO_(2+)等;n=0,1,2…;Z为H~+或一价阳离子;y=1,2,…。它们同其相应氧化型化合物比较具有引人注目的特性,但迄今尚未见到还原型化合物晶体结构文章,只是

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用XPS、TPR和同位素交换等技术,研究了钙钛石型催化剂La_(1-x)Sr_xFeO_(3-λ)中的活性氧种及其反应性能。在考虑晶格缺陷的基础上,认为以弱键和钙钛石中氧空位给合的α氧是这个催化体系中的活性氧种。当x值自0变化至1时,α氧量增加;当x>0.4时,α氧的反应性下降。在x<0.4的范围内,催化活性取决于α氧的浓度,而在x≥0.4的范围内,催化活性取决于α氧的反应性。此外,催化活性还同该体系分解气相氧的能力有关。

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本工作用扭辫法、红外光谱法及热分析法等研究了 1,2-聚丁二烯(1,2-PB)生胶的热氧老化性能及其机理。1,2-PB生胶的热氧老化可能是由于乙烯基双键打开进行碳-碳交联和醚式氧桥交联所致。1,2-链节间同立构含量的升高,导致聚合物热氧稳定性变差。1,2-PB生胶的热氧稳定性优于顺丁、丁苯和天然橡胶。防老剂 2246用量为1.0%时,对1,2-PB生胶有较好的稳定作用。

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本文系统地研究了轻稀土元素 La、Nd 等部分取代 YbBa_2Cu_3O(7-δ)化合物中的 Yb 对结构和超导电性所产生的影响。少量(约0.1摩尔比)轻稀土元素可有效抑制 YbBa_2Cu_3O(7-δ)化合物中杂相的生成,提高体系中 Cu~(3+)/Cu~(2+)之值。

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The effects of the timing of first feeding (0, 1 and 2 days after yolk exhaustion) and starvation on the point-of-no-return (PNR), survival and growth of laboratory-reared rock bream larvae were studied under controlled conditions. Larvae began to feed exogenously at 3 days after hatching (dah) and reached PNR on 54 h after yolk exhaustion at 22 +/- 1.5 degrees C. Larvae growth was significantly affected by the time of first exogenous feeding. The growth of 0 day delayed first feeding larvae was obviously faster than those of the other delayed first feeding larvae (P<0.05) whether at 7 dab (SL=3.40 mm, SGR=5.7, CV=4.0) or at 15 dah (SL=4.85 mm, SGR=6.1, CV=8.2) with a more uniform size distribution. Survival of 0 day delayed first feeding larvae and I day delayed first feeding larvae was 13% and 8% at the end of experiment, respectively, while no larvae survived up to 7 dah for 2 days delayed first feeding larvae and unfed larvae. Food resulted in a progressive deterioration of the larval digestive system and atrophy of skeletal muscle fibre. The ratios of head length to SL (standard length), body height to SL and eye diameter to SL were the most sensitive morphometric indices to detect the effects of fasting on larval condition. Present results showed that the combination of morphological and morphometric variables could be used to evaluate the nutritional condition of rock bream larvae. In order to avoid the potential mortality and gain better development, survival and growth in industrial production, the rock bream larvae must establish successful first feeding within 2 days after yolk exhaustion. (C) 2008 Elsevier B.V. All rights reserved.