离子色谱法快速连续测定锗和锡的研究

介绍了一种快速测定锗和锡的新方法──离子色谱法。锗和锡在双功能的分离柱上被分离后进行柱后显色反应,然后经可见检测器于５２０ｎｍ处检测。此法具有较高的灵敏度和选择性,整个分析过程仅需５ｍｉｎ,样品分析结果令人满意。     

Synergic Extraction of Uranium Thiocyanate by the Ternary System of ABC Species Composed of PMBP-TBP-(C6H5)4AsCI

The synergic extraction of uranyl thiocyanate with binary system of 1-phenyl-3-methy1~4-benzoylpyrazolone-5 (PMBP)and tributyl phosphate(TBP)or tetraphenylarsonium chloride [(C6H5)4AsCl] and ternary system of PMBP-TBP-(C6H5 )4AsCl was studied.There was an obvious synergic effect of uranium (VI)from thiocyanate medium in binary and ternary systems.The formation of a ternary extracted complex,(C6H5)4AsUO2.(NCS)A2 TBP,was confirmed by the slope method.A method was first proposed for the calculation of the equilibrium constant of ternary synergic reaction.     

离子色谱法测定增味剂中的5′-肌苷酸二钠和5′-鸟苷酸二钠

 建立了增味剂中5′-肌苷酸二钠和5′-鸟苷酸二钠的离子色谱分析方法。采用lonPacASll阴离子交换色谱柱,以20mmol／LNa2CO3一体积分数为15％的甲醇溶液为淋洗液,检测波长254um。方法已用于实际样品的测定。     

Determination of Monochloroacetic Acid and Dichloroacetic Acid for Quality Control of Acetic Acid Chlorination Industry by Ion Chromatography

An ion chromatographic method is described for the purpose of quality control in the process of monochloroacetic acid production. Using 2.5 mM NaOH–10% methanol as eluent, the simultaneous determination of acetic acid, monochloroacetic acid, dichloroacetic acid, and Cl⁻ was obtained in a single run. Monochloroacetic acid and dichloroacetic acid showed good linearity in the range 0.1–20 and 0.15–20 μg/ml and correlation coefficients were 0.9999 and 0.9998, respectively. The detection limits (signal-to-noise ratio 3:1) of monochloroacetic acid and dichloroacetic acid were 17 and 25 ng/ml. This simple, sensitive, and time-saving method can be applied for composition analysis in acetic acid chlorination production.     

可生物降解聚酯酰胺共聚物的合成与表征

以两种合成的酰胺二元醇和癸二酸为原料合成了可生物降解的聚酯酰胺共聚物,研究了该癸半晶性聚合物的合成、结晶及其生物降解性,并应用ＩＲ,＾１Ｈ ＮＭＲ,ＳＥＭ及ＤＳＣ进行了表征。     

The Synthesis and Application of the Mesoporous Molecular Sieves MCM-41 — A Review

We report a “delayed neutralization” process for the preparation of highly-ordered aluminosilicate MCM-41 molecular sieves with high thermal and hydrothermal stability, and sharp pore size distribution. However, the structural order and pore size are dependent on the carbon chain length. In the mixture surfactant systems, the pore size of the MCM-41 materials could be fine-tuned. The pore size can be extended from 2.5 to 4.5 nm by adding a suitable amount of hydrocarbons. The tubular morphology of the MCM-41 material of 0.3 to 10 micrometers diameter, where the wall consists of coaxial cylindrical pores of nanometers MCM-41, can be obtained by careful control of the surfactant-water content and the rate of condensation of silica. An optimum condition for automatic synthesis of the hierarchical TWT structure has been accomplished. The addition of 1-alkanols as cosurfactant would not only improve the order of the MCM-41 hexagonal structure but also promote the formation of micrometer-sized hierarchical materials, for example: tubules-within-tubule and uniform-sized hollow spheres of diameter 5.0 ± 1.0 μm. However, the inside of the micron spheres has intricate structures possessing various topological genus ranks. The MCM-41 is a good supporter for Molybdenum oxide catalysts. The rate of deactivation in the catalytic reaction of ethyl-benzene dehydrogenation to styrene increases in the order: M_T < M_P < SiO₂. The physically mixed samples have higher catalytic activity than impregnated ones.     

三异辛胺-硅胶柱高效液相色谱分离与测定矿石中微量金

研究用三异辛胺（ＴＩＯＡ）－硅胶柱反相萃取色谱分离、孔雀绿萃取光度法测定金（Ⅲ）、金回收率在９６％以上。应用于矿石中微量金匠测定,结果满意,测定的最大相对误差（ｎ＝５）为６．３％。     

M/C3N4/AC (M=Au,Pt,Ru)催化乙炔与二氯乙烷耦合反应:双功能催化剂性能如何?

聚氯乙烯是世界上产量最大的通用塑料,在日常生活的诸多领域具有广泛应用.按照原料来源划分,聚氯乙烯的工业生产方法主要有基于煤炭的电石法和基于石油的"平衡法".我国有丰富的煤炭资源,因此,电石乙炔法是合成聚氯乙烯的主要途径.该方法采用乙炔与氯化氢在活性炭担载氯化汞催化剂上进行氢氯化反应得到聚氯乙烯的单体氯乙烯.然而,由于汞...     

High-efficiency hyperfluorescent white light-emitting diodes based on high-concentration-doped TADF sensitizer matrices via spatial and energy gap effects

Despite the success of monochromatic hyperfluorescent (HF) organic light-emitting diodes (OLEDs), high-efficiency HF white OLEDs (WOLEDs) are still a big challenge. Herein, we demonstrate HF WOLEDs with state-of-the-art efficiencies, featuring a quasi-bilayer emissive layer (EML) composed of an ultrathin (0.1 nm) blue fluorescence (FL) emitter (TBPe) layer and a layer of thermally activated delayed fluorescence (TADF) sensitizer matrix heavily doped with a yellow FL emitter (TBRb, 3%). Based on an asymmetric high-energy-gap TADF sensitizer host (PhCzSPOTz), such an “ultrathin blue emitting layer (UTBL)” strategy endowed the HF WOLEDs with a record power efficiency of ∼80 lm W⁻¹, approaching the level of fluorescent tubes. Transient photoluminescence (PL) and electroluminescence (EL) kinetics demonstrate that the spatial separation of TBPe from the TADF sensitizer and TBRb, and the large energy gap between the latter two effectively suppress triplet leakage, in addition to suppressing triplet diffusion in the PhCzSPOTz matrix with anisotropic intermolecular interactions. These results provide a new insight into the exciton allocation process in HF white light-emitting systems.

A thermally activated delayed fluorescence host was developed to realize high-efficiency fluorescence white organic light-emitting diodes (WOLED) through spatial and energy gap effects.     

A Universal Cassette-Based System for the Dissolution of Solid Targets

Cyclotron-based radionuclides production by using solid targets has become important in the last years due to the growing demand of radiometals, e.g., ⁶⁸Ga, ⁸⁹Zr, ^43/47Sc, and ^52/54Mn. This shifted the focus on solid target management, where the first fundamental step of the radiochemical processing is the target dissolution. Currently, this step is generally performed with commercial or home-made modules separated from the following purification/radiolabelling modules. The aim of this work is the realization of a flexible solid target dissolution system to be easily installed on commercial cassette-based synthesis modules. This would offer a complete target processing and radiopharmaceutical synthesis performable in a single module continuously. The presented solid target dissolution system concept relies on an open-bottomed vial positioned upon a target coin. In particular, the idea is to use the movement mechanism of a syringe pump to position the vial up and down on the target, and to exploit the heater/cooler reactor of the module as a target holder. All the steps can be remotely controlled and are incorporated in the cassette manifold together with the purification and radiolabelling steps. The performance of the device was tested by processing three different irradiated targets under different dissolution conditions.