Oxygen diffusion in SrCe<Subscript>0.95</Subscript>Yb<Subscript>0.05</Subscript>O<Subscript>3−δ</Subscript>

¹⁸O/¹⁶O isotope exchange depth profiling (IEDP) combined with secondary ion mass spectrometry (SIMS) has been used to measure the oxygen tracer diffusivity of SrCe_0.95Yb_0.05O_3– between 800 °C and 500 °C at a nominal pressure of 200 mbar. The values of D* (oxygen tracer diffusion coefficient) and k (surface exchange coefficient) increase steadily with increasing temperature, and the activation energies are 1.13 eV and 0.96 eV, respectively. Oxygen ion conductivities have been calculated using the Nernst–Einstein equation. The transport number for oxide ions at 769 °C, the highest temperature studied, is only ~0.05. Moreover, SrCe_0.95Yb_0.05O_3– has been studied using impedance spectroscopy under dry O₂, wet O₂ and wet H₂ (N₂/10% H₂) atmospheres, over the range 850–300 °C. Above ~550 °C, SrCe_0.95Yb_0.05O_3– shows higher conductivity in dry O₂ than in wet O₂ or wet H₂; below that temperature the results obtained for the three atmospheres are comparable. Dry O₂ shows the highest activation energy (0.77 eV); the activation energies for wet O₂ and wet H₂ are identical (0.62 eV).Abbreviations HTPC high-temperature proton conductor - IEDP isotope exchange depth profiling - SIMS secondary ion mass spectrometryPresented at the OSSEP Workshop Ionic and Mixed Conductors: Methods and Processes, Aveiro, Portugal, 10–12 April 2003     

Synthesis and chelation properties of new polymeric ligand derived from 8-hydroxy-5-azoquinoline hydroxy benzene

8-Hydroxy-5-azoquinoline phenyl methacrylate-formaldehyde (8H5AQPMA-F) macromonomer was prepared from methacryloyl chloride with condensation products of 8-hydroxy-5-azoquinoline phenol-formaldehyde, and polymerized in DMF at 70 °C using benzoyl peroxide as free radical initiator. Poly(8H5AQPMA-F) was characterized by infrared and nuclear magnetic resonance spectroscopic techniques. Polychelates were obtained when the DMF solution of the resin containing few drops of ammonia was treated with the aqueous solution of Cu(II)/Ni(II). Elemental analysis of the polychelates indicates that the metal to ligand ratio was about 1:2. The IR spectra of polychelates suggest that the metals were coordinated through the oxygen of the phenolic-OH group and nitrogen of the quinoline ligand. The DRS and magnetic moment data indicate a square planar for Cu(II) complex whereas octahedral for Ni(II) complex. The TGA data revealed the thermal stability of the resin and the polychelates. X-ray diffraction study revealed the incorporation of the metal ions significantly enhanced the degree of crystallinity. The sorption properties of the chelate-forming resin towards various divalent metal ions [Cu(II) and Ni(II)] were studied as a function of pH and electrolyte.     

Ce0.6Zr0.35Y0.05O2和Pr0.6Zr0.35Y0.05O2催化剂表面上CO氧化和18O-16O交换反应的研究

测定了在Ce0.6Zr0.4O2,Ce0.6Zr0.35Y0.05O2,Pr0.6Zr0.4O2和Pr0.6Zr0.35Y0.05O2 (分别表示为CZ,CYZ,PZ和PYZ)样品表面上的CO氧化反应和18O-16O 同位素交换反应.结果表明: 在CZ和PZ系列固熔中掺杂Y3 离子可以改善晶格氧的迁移速度;PZ和PZY的晶格氧比CZ 和CZY 的晶格氧具有更高的氧化反应活性.其原因是将Y3 掺杂到Ce0.6Zr0.4O2 或Pr0.6Zr0.4O2晶格中,增加了样品的氧空位浓度,从而提高了晶格氧的迁移性质,而PrOx比CeO2具有更低温度的氧化还原性质,因此PZ和PZY的晶格氧比CZ 和CZY 的晶格氧具有更高的氧化反应活性.     

Prospects of Sol-Gel Process for Spectral Hole-Burning Glasses

Persistent spectral hole burning was studied in Eu³⁺ ions-doped Al₂O₃-SiO₂ glass prepared by a sol-gel method. The gel synthesized by the hydrolysis of Si- and Al-alkoxides and EuCl₃·6H₂O was heated in air and hydrogen gas atmospheres. For the glass heated in air to contain OH bonds, the hole was formed by the photoinduced rearrangement of the OH bonds surrounding the Eu³⁺ ions, and was thermally refilled and erased above 200 K. On the other hand, the glass heated in hydrogen gas showed the hole spectrum above 200 K. It was found that the hole depth was independent of the temperature and was 7% of the total intensity at room temperature. The proposed mechanism was the electron transfer between the Eu³⁺ ions and the defect centers formed in glass matrix.     

Chemically assisted ion beam etching of silicon and silicon dioxide using SF6

A chemical flux of sulfur hexafluoride (SF₆) in conjunction with low-energy Ar-ion bombardment has been used for chemically assisted ion beam etching (CAIBE) of silicon and silicon dioxide. The study has shown a large degree of independent control over the selectivity and anisotropy in dry etching. The total etch rate could be controlled by varying either the Ar-ion milling parameters or the chemical flux of SF₆. Etch rate enhancement of 7–8 for silicon and 3–4 for silicon dioxide have been obtained over pure physical etching.     

Simultaneous determination of carbohydrates and organic acids in beer and wine by ion chromatography

The simultaneous determination of mono-organic acids and carbohydrates by ion chromatography with both conductometric and pulsed amperometric detection is described. The carbohydrates, such as mannitol, arabinose, glucose, fructose, lactose, sucrose, raffinose, and maltose, as well as monoorganic acids including acetate, glycolate, formate, pyruvate, and fluoride are separated as anions by ion-exchange chromatography with 0.080 mol/L sodium hydroxide eluent at 1 mL/min within 12 min. Carbohydrates are determined by pulsed amperometric detection and mono-organic acids are determined by suppressed conductivity detection. The species in beverages are determined.     

离子色谱柱切换技术同时测定食品中的多种成分

采用离子色谱柱切换技术同时测定了保留性质差别较大的有机酸以及不同价态的无机阴离子。由于柱切换基本不影响色谱基线,该法有较高的灵敏度。同时测定了食品中的乙酸,山梨酸、苯甲酸、糖精、氯离子和磷酸根。     

Cu(II)-Cu(Hg)体系在蔗糖水溶液中的电化学行为

糖及其聚合物有着重要的生理功能,研究它们的热力学性质具有重要的意义[1 5]。本文考察Cu(II)在蔗糖水溶液中的电化学行为,获得了一些重要信息。1　实验部分使用试剂均为分析纯。蔗糖(北京化学试剂总厂)在343K时真空干燥6h。LiClO4(上海化学试剂总厂)在403K时减压干燥后保存在干燥器中。硝酸铜(北京化学试剂总厂)。所用溶液均采用重量法用二次蒸馏水配制。配好的溶液测定前用通过焦性没食子酸溶液的氮气来除氧。测定温度为298±1K。极谱和伏安测定在微机电化学分析系统(LK98A型)上进行,该机由天津市兰力科化学电子高技术有限公司制…     

离子交换-双氧水氧化法制备纳米CeO2晶体

以99.995% Ce(NO₃)₃和强碱性阴离子交换树脂为原料，采用离子交换-双氧水氧化法合成制备出纳米CeO₂晶体。并就离子交换反应中的Ce³⁺浓度、树脂加入速度和离子交换温度及H₂O₂加入速度等条件对CeO₂粒径的影响进行了探讨，得出了离子交换-双氧水氧化法制备纳米CeO₂晶体的最佳工艺条件。FTIR、TEM分析表明，离子交换法无需对合成的Ce(OH)₃溶胶进行洗涤即可去除NO₃^-、CO₃^2-等阴离子杂质，并用H₂O₂将该溶胶氧化，经真空干燥可制得粒径分布均匀，平均晶粒尺寸约3 nm，高纯度的CeO₂粉体。     

Trace anion determination in concentrated hydrofluoric acid solutions by two-dimensional ion chromatography II. Method performance study with a hydroxide eluent and a low noise suppressor

The two-dimensional ion exclusion chromatography/ion chromatography (ICE-IC) approach is considered to be the method of choice for the determination of trace anions in concentrated hydrofluoric acid (48-50%, w/w). In order to achieve lower detection limits, this method was for the first time used with electrolytically generated and purified hydroxide eluents in combination with a low noise electrochemical suppressor. Compared to carbonate based eluents, the achieved gain in peak height sensitivity for chloride, sulfate, nitrate and phosphate is a factor of 6, 7, 16 and 13, respectively. The instrumental detection limits, based on the background noise, are 2, 0.2, 0.4 and 1.4 microg/kg HF 50% (w/w) for the same anions. Their method detection limits, calculated according to SEMI, are all within the 6-10microg/kg HF 50% (w/w) range and thus at least 10 times lower than the current Tier C grade requirements. The chromatographic run time could be shortened with some 10 min by the use of a relatively fast high-capacity hydroxide selective anion exchange column.