410 resultados para Pr_(1-x)K_xMnO_3


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The electrical conductivities of pernigraniline after ion implantation with potassium ions were studied experimentally. Pernigraniline films were irradiated with doses ranging from 1 x 10(13) to 1 x 10(17) K+ ions/cm2 at 40 keV. The electrical conductivit

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A multi-cylinder microelectrode coupled with a conventional glassy carbon disc electrode (MCM/GC) was prepared and characterized using cyclic voltammetry and chronoamperometry. It was demonstrated that in the same way as one observed a steady-state current at closely spaced microelectrodes when redox recycling takes place, the same effect can be obtained with the MCM/GC device. The experimental results obtained with K3Fe(CN)6 solutions were compared with a previously developed theory. Further, it was demonstrated that with a carbon fibre MCM/GC device, the voltammetric behaviour of dopamine is greatly improved by virtue of redox recycling, hence giving high sensitivity. The steady-state collection current was linearly related to dopamine concentration in the range 1 X 10(-4) to 5 x 10(-7) Mol l-1, and the detection limit was 2 x 10(-7) mol l-1. The influence of coexisting ascorbic acid was also investigated. This device was applied successfully in the determination of dopamine hydrochloride in pharmaceutical preparations.

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Amperometic flow measurements were made at +0.55 V (vs. Ag/AgCl) in 0.1 mol l-1 KOH electrolyte with an Ni(II) chemically modified electrode (CME) with an Eastman-AQ polymer film. The use and characteristics of a Ni(II)-containing crystalline and polymer-modified electrode obtained by a double coating step as a detector for amino acids in a flow-injection system using reversed-phase liquid chromatography are described. The detection of these analytes is based on the higher oxidation state of nickel (NiOOH) controlled by the applied potential. The electroanalytical parameters and the detection current for a series of amines and amino acids were investigated. The use of such a CME in the flow-injection technique was found to be suitable in a solution at low pH. The linear range for glycine is 5 X 10(-6)-0.1 mol 1-1 with a detection limit of 1.0 X 10(-6) mol l-1. A 1 X 10(-4) mol 1-1 mixture of serine and tyrosine was also detected after separation on an Nucleosil C18 column.

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A glassy carbon electrode (GCE) modified with palladium provides excellent electrocatalytic oxidation of hydrogen peroxide. When the electrolyte contains palladium chloride and glucose oxidase, the GCE can be modified by electrochemical codeposition at a given potential. The resulting modified surface was coated with a thin film of Nation to form a glucose sensor. Such a glucose sensor was successfully used in the flow-injection analysis of glucose with high stability and anti-poisoning ability. It gave a detection limit of 1 X 10(-7) M injected glucose, with a linear concentration range of 0.001-8 mM. There is no obvious interference from substances such as ascorbate and saccharides.

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考察了Li-Ni-La-O系催化剂的组成、结构及反应条件对甲烷氧化偶联反应活性的影响.在780℃、CH_4:O_2:N_2=2:1:7、空速15000h~(-1)时,C_2烃收率可达25.8%.XRD、IR、XPS及SEM等的结构分析表明,在LiLa_(1-x)Ni_xO_2催化剂中,当0.1≤x≤0.9时,该催化剂由LiNiO_2和LaNi_(1-y)Li_yO_(4-λ)两相组成,x<0.3时出现了LiLaO_2相,La_2Ni_(1-y)Li_yO_(4-λ)是甲烷氧化偶联的主要活性相,活性位Li~+-O~--Ni~(2+)数量的增加是活性提高的主要原因.LiNiO_2和LiLaO_2也有催化活性,它们与La_2Ni_(1-y)Li_yO_4间的协同作用也可能是催化活性增强的原因.

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本文着重研究了聚丙烯纤维在等离子体中处理后的吸湿性能和染色性能的改变情况。结果表明经等离子体处理过的样品其吸湿性能和染色性能都有很大的改善。处理过的样品回潮率大约为未处理样品的120~400%,其染色性能从未处理的5级提高到1级的标准。处理后聚丙烯纤维力学性能基本没有变化。X光电子能谱分析表明吸湿性能和染色性能改变是由于经等离子体处理后丙纶表面引入含氧、含氮基团所致。

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用XRD、IR、XPS和SEM等方法研究了混合氧化物LiLa_(1-x)Mn_xO_2的结构和它们对甲烷氧化偶联的催化性能。结果表明,随着MnO_2的变化,可形成一系列复合氧化物,其中三元复合氧化物La_2Mn_(1-y)Li_yO_4是甲烷氧化偶联的活性相,由于Li~+部分取代Mn~(2+)形成Li~+-O~--Mn(2+)缺陷簇,增加了活性氧种的浓度和再生速度是这种氧化物具有较高甲烷偶联活性的主要原因。脉冲实验证明,CH_4脱氢生成CH_3·偶联生成C_2H_6,进一步氧化脱氢生成C_2H_4都可在催化剂表面完成,而CO和CO_2是在气相反应中生成的。在780℃C_2收率可达23.9%。

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The adsorption of bis(4-pyridyl)disulphide (PySSPy) and 4.4'-bipyridyl (PyPy) on a gold electrode was studied using cyclic voltammetry. The adsorption isotherms and equilibrium constants (1 X 10(6) mol-1 l for PyPy and 6 x 10(6) Mol-1 l for PySSPy) were determined. The effect of pH on the electrochemical behaviour of cytochrome c was studied on the PySSPy-modified gold electrode. The results show that cytochrome c can only transfer electrons on a deprotonated electrode surface. When the pH is decreased, the standard heterogeneous rate constant of cytochrome c on the modified gold electrode decreases and the electrochemical behaviour changes from a quasi-reversible to an irreversible process.

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Electrode capacitance and photocurrent spectra of electrodeposited polycrystalline Hg1-xCdxTe thin films of varying (1-x) were measured in polysulfide redox solution, hence the flatband potentional PHI(fb) and the bandgap E(g) of Hg1-xCdxTe thin films obtained. It was of interest to find out that only the location of conduction band E(c) shifts negatively with increasing (1-x) while the valence band E(v), is almost constant. The experimental open circuit photovoltage V0 is smaller than theoretical value V(max) calculated through flatband potential PHI(fb), therefore there is a possibility of promoting the experimental open circuit photovoltage.

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A conducting polyaniline (PAn) film modified glassy carbon (GC) electrode was prepared by electrochemical polymerization. The electrochemical behavior of ascorbic acid (AH(2)) in aqueous solution at this PAn modified electrode was studied in detail. The experimental results show that PAn film modified electrode has good electrocatalytic activity on the oxidation of ascorbic acid in aqueous solution over a wide range of pH value, among which pH 4 is the optimum condition. The oxidation process of ascorbic acid at PAn film electrode can be regarded as an EC catalytic mechanism. The kinetic process of the catalytic reaction was investigated by rotating disk electrode (RDE) coated with PAn films. The rate constant of the catalytic reaction was evaluated. The catalytic peak currents are proportional to the concentrations tions of ascorbic acid in the range of 5 x 10(-2)-1 x 10(-6) mol . L-1. The PAn film elec trodes give very stable responce for the oxidation of ascorbic acid. The present investigation shows the posibility of using PAn film modified electrode for the determination of ascorbic acid.

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合成了单元化学式为-Cu[(CH_3O)_2PO_2]_2-的铜(Ⅱ)与磷酸二甲酯的配位聚合物。测定了4000—100cm~(-1)谱区内的红外光谱,讨论了某些谱带的归属,解释了配位化合物形成后的光谱变化。由单晶X-射线衍射法确定此配合物的晶体属单斜晶系,空间群为P2_1/c,晶胞参数a=1.0704(4),b=0.5093(2),c=1.9737(6)nm;β=96.23(3)°;V=1.0696(6)nm~3;Z=4.M=313.5,F(000)=636e,D_c=1.943g·cm~(-3)。铜与五个配体中的五个非酯氧配位成四角锥体,相邻两铜原子以对称的“O—P—O”桥和不对你的“O—P—O”桥相连,形成一维链状配位聚合物。

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本文用高温固相扩散反应方法及坩埚下降法制备了KMgF_(3~-)Ce~(3+)及KMg_(1-x)M_xF_(3~-)Ce~(3+)(M=Be~(2+),Ca~(2+))的粉末样品及KMgF_(3~-)Ce~(3+)单晶,测定了它们的激发光谱和发射光谱,发现KMgF_(3~-)Ce~(3+)中存在两种不同的发射中心,且证明了这是不同的电荷补偿途径所致,而不是Ge~(3+)占据了不同的阳离子格位所致.通过X射线四圆衍射仪的检测及Be~(2+)和Ca~(2+)对KMgF_(3~-)Ce~(3+)中Mg~(2+)取代后的光谱变化,推断Ce~(3+)占据KMgF_3中K~+的格位.

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用X射线衍射和程序升温脱附方法研究了八个La-Ce-Co氧化物催化剂的结构及其氧的性能,试验了不同催化剂氨氧化反应前后氧的程脱并比较了其脱出氧的变化。测定了催化剂活性、组成及元素价态。发现催化剂的活性与三价钴离子的浓度成正比。催化剂中晶格氧的再生能力强,即氧化还原性能好,催化活性就高。结果表明,氨在La-Ce-Co氧化物体系催化剂上的氧化可能遵循Redox机理。Co~(3+)是活性中心。在催化剂中以少量Ce~(4+)取代La~(3+),可在催化剂中产生阳离子空位La_(1-x)CoO_(3+λ),有利于Co~(3+)的稳定加速体相中氧和电子的传递,促进催化剂的再氧化速度。从而提高催化剂的活性。

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在工业生产中NH_3氧化制HNO_3目前仍采用铂网催化剂。我们曾对稀土、过渡金属复合氧化物A_(1-x)A′_xBO_3型催化剂进行了一系列研究,其A,A′是碱土和稀土金属,B是Co,Fe,Mn,Ni等过渡金属元素。这类催化剂不仅活性高,HNO_3的单收率可达98%以上,而且具有良好的稳定性,但其寿命不如铂金.

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研究了Y_(1-x)Ag_xBa_2Cu_3O_(7-y)体系的结构。当x≤0.15时.该体系是固溶体.当0.150.5时,体系失去超导电性。在固溶体范围,Ag的置换改善了纯的YBCO脆性,增加了材料的机械强度,改善了颗粒弱连接.使体系的Jc从94.6A/cm~2提高到362A/cm~2。