Determination of hydroxylamine by capillary electrophoresis electrochemical detection with a palladium-particle modified carbon fiber microdisk array electrode

A highly dispersed ultramicro palladium-particle modified carbon fiber microdisk array electrode (Pd-CFE) was employed for capillary electrophoresis-electrochemical (CEEC) detection of hydroxylamine (HA). The Pd particles obtained were in the nanometer scale, had a high electrocatalytic activity towards HA and exhibited good reproducibility and stability. A linear relationship between the current and the analyte concentration was found between 5 x 10(-6) and 1 x 10(-3) mol/l of HA with a correlation coefficient of 0.9992. The detection limit was 5 x 10(-8) mol/l. The applicability of the method for the determination of HA in river water and waste water was investigated.

Probe beam deflection study of the ion exchange between Prussian blue film or indium hexacyanoferrate film and electrolyte solutions

Probe beam deflection(PBD) technique together with electrochemical techniques such as cyclic voltammetry was used to study the ion exchange in prussian blue(PB) film and its analogue indium hexacyanoferrate (InHCF) chemically modified electrodes, The ion exchange mechanism of PB was verified as following: K2Fe2+FeI(CN)(6)(-e--K+)reversible arrow(+e-+K+)KFe(3+)Fe(I)(CN)(6)(-xe--xK+)reversible arrow(+xe-+xK+) [Fe3+FeI(CN)(6)](x)[KFe3+FeI(CN)(6)](1-x) where on reduction in contact with an acidic KCl electrolyte, H+ enter PB film before K+. Both the cations and anions participate concurrently in the redox process of InHCF, meanwhile K+ ion plays a major role in the whole charge transfer process of this film with increasing radii of anions.

Li_8SiN_4-Li_3N-BN体系中立方BN转化行为的研究

研究了高温高压下x·Li_8SiN_4-0.1(1-x)·Li_3N-0.9(1-x)·BN体系中立方氮化硼(cBN)的转化行为。Li_8SiN_4的存在可显著改善cBN晶体的发育,提高晶体质量。在4.2～5.5GPa,1340～1750℃范围内确定了x=4.8％时体系的cBN转化区,并对转化区内cBN转化率、平均生长速度、成核速度及破碎强度与转化温度和压力的关系进行了研究。

THE EFFECT ON PHYSICAL-PROPERTIES OF THE SUBSTITUTION OF CA OR BA FOR SR IN NDSRNIO4

A new solid solution series, NdSr(1-x)M(x)NiO(4) (M = Ca: 0.0 less than or equal to x less than or equal to 1.0; M = Ba: 0.0 less than or equal to x less than or equal to 0.6), was synthesized by solid state reaction, and the structures, magnetic and electrical properties and optical spectra of this series have been studied. All the samples crystalized in tetragonal systems, with the exception of NdCaNiO4, which crystallized in the orthohombic system. IR spectra of NdSr1-xCaxNiO4 indicated that the lengths of two Ni-O bonds decrease with increasing Ca content. The electrical conduction changed from metallic-type to semiconductive-type when x greater than or equal to 0.4 (M = Ca, Ba), and the room temperature resistivities of NdSr1-xCaxNiO4 increased with the increase of Ca content. Magnetic susceptibility measurements revealed that Ni+3 ions in all the samplies were in low-spin state over the temperature range 77-300 K.

A novel in-situ spectroelectrochemical technique with probe beam deflection: For study of the ion exchange between films on electrode surface and solutions

A novel in-situ spectroelectrochemical technique, the combination of probe beam deflection (PBD) with cyclic voltammetry (CV), was used to study the ion exchange process of prussian blue(PB) modified film electrode in contact with various electrolyte solutions. The ion exchange mechanism was verified as following: (K2Fe2+FeII)(CN)(6) -e(-)-k(+)reversible arrow +e(-)+k(+) (KFe3+FeII)(CN)(6) -ke(-)-xk(+)reversible arrow +xe(-)+kk(+) [(Fe3+FeIII)(CN)(6)](x)[(KFe3+FeII)(CN)(6)](1-x) where on reduction PB film in contact with an acidic KCl electrolyte, it was confirmed that protons enter into the PB film before K+ cations.

绿辉石固溶体NaAlSi_2O_6-CaMgSi_2O_6的合成和高压下熔化过程研究

在2×10~9～5×10~9Pa,1 000～2 300℃下合成了由二元组分NaAlSi_2O_6(Jadeit)-CaMgSi_2O_6(Diopside)构成的绿辉石,通过XRD分析数据计算了绿辉石Jd_xDi_(1-x)的晶胞参数随组成变化的规律。采用高温高压淬火法和XRD研究了Jd_xDi_(1-x)(x=0～1.0)高压下(2×10~9～5×10~9 Pa)的固溶关系,并根据Jd_xDi(1-x)的固溶相图计算了不同压力下的熔化热。

MF_2:Eu,Ce(M=Ca,Sr,Ba)中稀土离子的价态变化

我们已经实验证明并报道了Eu-Tb之间、Ce-Yb之间的电荷转移.本文首次实验证实了Ce~(3+)离子和Eu~(3+)离子之间电荷转移现象的存在,进一步阐述了稀土价态与其电子组态共轭特征的相关性.1 实验部分1.1 试剂CaF_2,SrF_2,BaF_2,NH_4HF_2、氢氟酸、盐酸均为分析纯,EuF_3和CeF_3分别由高纯Eu_2O_3(99.95%)及CeO_2(99.99%)自制.1.2 MF_2:Eu,Ce体系的合成按化学计量比(MF_2:X%CeF_2,y%EuF_3;X=1,y=0,0.1,0.3,0.5,1;X=0,0.05,0.1,0.3,0.5,y=1)准确称取原料,放人玛瑙研钵中充分研混后装入刚玉柑涡中,置于管状炉内(用氢气

ELECTRICAL CHARACTERIZATION INDUCED IN PERNIGRANILINE BY POTASSIUM-ION IMPLANTATION

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

PREPARATION AND CHARACTERIZATION OF A MULTICYLINDER MICROELECTRODE COUPLED WITH A CONVENTIONAL GLASSY-CARBON ELECTRODE AND ITS APPLICATION TO THE DETECTION OF DOPAMINE

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.

AMPEROMETRIC DETECTION OF AMINO-ACIDS IN A FLOW-INJECTION SYSTEM WITH A NICKEL(II)-MODIFIED ELECTRODE WITH AN EASTMAN-AQ POLYMER FILM

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.

FLOW-INJECTION ANALYSIS OF GLUCOSE AT AN AMPEROMETRIC GLUCOSE SENSOR-BASED ON ELECTROCHEMICAL CODEPOSITION OF PALLADIUM AND GLUCOSE-OXIDASE ON A GLASSY-CARBON ELECTRODE

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.

Li-Ni-La-O系复合氧化物催化剂上甲烷氧化偶联的研究

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.

聚丙烯纤维的等离子体改性研究

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。

甲烷氧化偶联La-Mn-Li系复合氧化物催化剂的研究

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%。

EFFECT OF PH ON THE ELECTRON-TRANSFER OF CYTOCHROME-C ON A GOLD ELECTRODE MODIFIED WITH BIS(4-PYRIDYL)DISULPHIDE

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.