双马来酰亚胺增韧研究Ⅱ.链扩展双马来酰亚胺及其树脂的合成及表征

合成了一系列结构不同和链长短不一的双马来酰亚胺，并对其结构和性能作了表征，同时研究了它们的固化反应和固化产物的性能。用双马来酰亚胺和二烯丙基化合物反应制造了增韧树脂，研究了该树脂的固化和热稳定性。     

实验化学的名师巨匠——本生

本生是一代实验化学的名师巨匠,他的一生在化学发展史上留下了光辉的一页。在几十年的科学实验和研究中,他潜心钻研化学理论,不断提高自己的实验技能。他亲自设计和改进了诸多实验仪器和装置,并为此做出了发明和创造。他的主要贡献有:创立了光谱分析法,发现了铯和铷两种元素,发明了本生灯和本生电池,并在化学工业的掘起和发展中做出了重要的贡献。     

环氧乙烷和环氧丙烷开环聚合

环氧乙烷和环氧丙烷的开环聚合产物在表面活性剂工业和聚氨酯工业得到了极为广泛的应用.本文综述了近几年来发展的用于环氧乙烷和环氧丙烷开环聚合的各类催化剂体系,分别讨论了各类催化剂体系对环氧乙烷和环氧丙烷的不同作用机制,考察了反应物结构对反应活性和选择性的影响,重点介绍了配位络合催化剂体系在环氧乙烷和环氧丙烷开环聚合反应中的应用,并指出了今后研究的方向.     

新型大环超分子化学:从杂杯芳烃到冠芳烃——纪念黄志镗先生诞辰90周年

本文介绍了杂杯芳烃和冠芳烃的研究起源,总结了杂杯芳烃和冠芳烃的设计与合成、构象和大环空腔结构特征,展示了杂杯芳烃和冠芳烃的分子识别和组装性质,概述了杂杯芳烃和冠芳烃在功能材料的制备中的应用,展望了大环超分子化学未来的发展方向。     

同位素分离(摘要)

同位素是Soddy首先从放射性元素中发现的。然后Aston用质谱法分离了同位素,接着Lindemann探索了其他的分离方法。Harkins 和他的学生Mul-likan分离了汞同位素并研究了其他分离方法。Hertz和Keeson 分别用扩散法和分馏法分离了Ne的同位素。不久,Urey用蒸馏液氢和电解水的方法浓缩了     

Spin-Free理论与Woodward-Hoffmann规则——丁二烯体系电环合反应的研究

用Spin-Free理论,对丁二烯体系电环合反应进行了研究,得到了基态和各激发态的位能面,解释了加热和加光反应机理和选择定则,对其中的单态和三态光化反应作了初步探讨并求出了有关的活化能。     

钙钛矿型高温质子导体研究进展

介绍了钙钛矿型和复合钙钛矿型化合物的结构、常用的制备方法和传导性质,详细分析了其传导机理,评述了其研究进展和在气体传感器、固体燃料电池、有机物加氢和脱氢以及常压电化学合成氨等方面的应用,展望了应用前景和发展趋向.     

苯并三唑和8-羟基喹啉对铜的缓蚀协同作用

通过电化学极化曲线和电化学阻抗谱研究了苯并三唑（BTA）和8 羟基喹啉（HQ）对铜的缓蚀协同作用， BTA和HQ复配使用后提高了电极的膜电阻，降低了电极的膜电容，增强了对铜腐蚀的抑制作用.通过MM2分子力学程序和PPP SCF量子化学方法优化计算了BTA和HQ的分子结构参数，分析讨论了它们之间的缓蚀协同效应.     

花粉蛋白和多糖的研究

从葡萄和罂粟花粉中分别纯化得RP3I和PSPP1-4肽, 测定了它们的生理活性,并合成了PSPP1以外的肽, 从Typha Angustifilia和codonopsis pilosula花粉获得了TA-C和CPA-E多糖, 并研究了它们的部份特征和结构。     

我国金属中气体分析的回顾

近几年来,我国金属中气体分析得到了很大的发展。使用了一些新的技术和方法;研制了各种型号的新仪器,制定了部分标准方法和制备了部分标准试样。同时召开了数次全国性和地区性的报告会和鉴定会,肯定了成果,交流了经验。本文仅就我国金属中气体分析的进展作一简要的回顾。一、热源和测试方法我国金属中气体(指氧、氮、氢)分析,开展较早的单位是科学院金属研究所、有色总公司北京有色金属研究总院和冶金部钢铁研究总院。他们在50年代就建立了真空熔融微压法的实验装置,开展了黑     

Synthesis and structural characterization of complexes of a DO3A-conjugated triphenylphosphonium cation with diagnostically important metal ions

To understand the coordination chemistry of a DO3A-conjugated triphenylphosphonium (TPP) cation, triphenyl(4-((4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl)methyl)benzyl)phosphonium (DO3A-xy-TPP), with diagnostically important metal ions, In(DO3A-xy-TPP)+, Ga(DO3A-xy-TPP)+, and Mn(DO3A-xy-TPP) were prepared by reacting DO3A-xy-TPP with 1 equiv of the respective metal salt. All three complexes have been characterized by elemental analysis, IR, ESI-MS, NMR methods (for In(DO3A-xy-TPP)+ and Ga(DO3A-xy-TPP)+), and X-ray crystallography. Results from HPLC concordance experiments show that (111)In(DO3A-xy-TPP)+ and In(DO3A-xy-TPP)+ have the same composition. The solid-state structures of In(DO3A-xy-TPP)+ and Mn(DO3A-xy-TPP) are very similar with DO3A being heptadentate in bonding to In(III) and Mn(II) in a monocapped octahedral coordination geometry. Because of the smaller size of Ga(III), the DO3A in Ga(DO3A-xy-TPP)+ is only hexadentate with four amine-N and two carboxylate-O atoms bonding to Ga(III). One carboxylic acid group in DO3A is deprotonated to balance the positive charge of Ga(III). The coordination geometry of Ga(DO3A-xy-TPP)+ is best described as a distorted octahedron. The NMR data shows that the coordinated DO3A in In(DO3A-xy-TPP)+ and Ga(DO3A-xy-TPP)+ is symmetrical in aqueous solution. There is no dissociation of the acetate chelating arms in In(DO3A-xy-TPP)+ and Ga(DO3A-xy-TPP)+, providing indirect evidence for the high solution stability of (111)In(DO3A-xy-TPP)+ and (68)Ga(DO3A-xy-TPP)+.     

Enhanced Nucleation and Crystallization in PLA/CNT Composites via Disperse Orange 3 with Corresponding Improvement in Nanomechanical Properties

The potential for the material property improvement through the addition of carbon nanotubes (CNTs) in composite materials is often limited due to CNT agglomeration. In this work, Disperse Orange 3 (DO3) was investigated to determine its effectiveness in dispersing CNTs in a poly (lactic acid) (PLA) matrix. First, adsorption studies of DO3 onto CNTs were performed to determine the appropriate amount of DO3 to add so that the CNT surface will be nearly saturated with DO3 while limiting the excess DO3 dissolved in the polymer. The resultant improvements in the mechanical properties were determined via nanoindentation. Highly stable dispersion of CNTs in tetrahydrofuran with DO3 was observed 72 hours after sonication. Scanning electron microscopy confirmed that DO3‐functionalized CNTs were able to separate and disperse well inside of the PLA matrix. Addition of DO3 to the nanocomposite resulted in an increase in the glass transition temperature and crystallinity of the composite due to the more effective dispersion of the nanofiller which serves as a nucleation agent. The CNTs treated with DO3 also increased the elastic modulus and hardness of the composite compared to neat PLA and untreated PLA‐CNT composites. From this study, DO3 was demonstrated to be an effective dispersing agent in the solvent and the PLA matrix which allowed for enhanced crystallization and improved nanomechanical properties in the resultant composite.     

Flow-injection analysis for hypoxanthine in meat with dissolved oxygen detector and enzyme reactor

A low cost flow-injection analysis (FIA) with a dissolved oxygen (DO) detector and a xanthine oxidase immobilized column for the analysis of hypoxanthine as an index to determine degree of aging in meat was developed for quality control in the food industry. In this system, hypoxanthine is oxidized by an enzyme reaction with xanthine oxidase immobilized on the column to produce xanthine. Then the catalytic reaction between hypoxanthine and DO with xanthine oxidase proceeds with the DO concentration decreasing in the stream of the flow system. Decrease in the DO concentration was monitored by a DO detector located downstream of the flow system. This decrease in DO concentration was proportional to the hypoxanthine concentration. For detecting the decreased DO concentration efficiently a flow-through cell with a polarographic-type DO sensor was specially designed. As a result, a linear working curve was obtained from 3.68 × 10⁻⁵ to 1.84 × 10⁻³ M hypoxanthine concentrations with this FIA system. We applied the present system with a DO detector for the determination of hypoxanthine in meat samples and compared the results with those obtained by the conventional HPLC method. The data obtained with the present FIA method were in fairly good agreement with those obtained by the conventional HPLC method for the meat samples. Correlation factor and regression line between the two methods were 0.998 and Y= 1.51X-32.64 respectively. We concluded that the present FIA system with a DO detector was suitable as a simple, easy to handle and reliable instrument for quality control in the food industry.     

Immunosensor for Detection of the Textile Dye Disperse Orange 1 Based on Non‐conventional Competitive Assay

Textile dyes appear as an important class of compounds that has become a matter of public concern and a serious challenge for scientists and environmentalists due to their large‐scale production and extensive application. In this work, a non‐conventional competitive‐type amperometric immunosensor was successfully developed for detection of the textile dye Disperse Orange 1 (DO1). The DO1 was magnetically captured and separated from the sample solution using magnetic particles (MP) functionalized with the antibody anti‐DO1 and with HRP and gold electrodes were modified with the conjugate DO1‐BSA. Molecules of DO1 immobilized on the electrode surface and DO1 captured by MP compete for antibody binding sites. As a result, the amperometric signal decreases with increasing target DO1 concentration at the capture step, because this decreases, the attachment between the HRP coated MP and the electrode. This strategy allowed us to determine DO1 at the low detection limit of 0.87 ng mL^?1 with great specificity. Also, there were good recoveries for detection of the textile dye in river water samples without the need of sample pre‐treatment. The competitive amperometric immunosensor shows applicability for the determination of small molecules that cannot be determined by conventional competitive or sandwich immunosensors.     

Comprehensive Evaluation of the Physicochemical Properties of LnIII Complexes of Aminoethyl‐DO3A as pH‐Responsive T1‐MRI Contrast Agents

N‐Substituted aminoethyl groups were attached to 1,4,7,10‐tetraazacyclododecane‐1,4,7‐triacetic acid (DO3A) with the aim to design pH‐responsive Ln^III complexes based on the pH‐dependent on/off ligation of the amine nitrogen to the metal ion. The following ligands were synthesized: AE ‐ DO3A (aminoethyl‐DO3A), MAE ‐ DO3A (N‐methylaminoethyl‐DO3A), DMAE ‐ DO3A (N,N‐dimethylaminoethyl‐DO3A) and MEM ‐ AE ‐ DO3A (N‐methoxyethyl‐N‐methylaminoethyl‐DO3A). The physicochemical properties of the Ln^III complexes were investigated for the evaluation of their potential applicability as magnetic resonance imaging (MRI) contrast agents. In particular, a ¹H and ¹⁷O NMR relaxometric study was carried out for these Gd^III complexes at two different pH values: at basic pH (pendant amino group coordinated to the metal centre) and at acidic pH (protonated amine, not interacting with the metal ion). Eu^III complexes allow one to estimate the number of inner‐sphere water molecules through luminescence lifetime measurements and obtain some structural information through variable‐temperature (VT) high‐resolution ¹H NMR studies. Equilibria between differently hydrated species were found for most of the complexes at both acidic and basic pH. The thermodynamic stability of Ca^II, Zn^II, Cu^II and Ln^III complexes and kinetics of formation and dissociation reactions of Ln^III complexes of AE ‐ DO3A and DMAE ‐ DO3A were investigated showing stabilities comparable to currently approved Gd^III‐based CAs. In detail, higher total basicity (Σlog K_i^H) and higher stability constants of Ln^III complexes were found for AE ‐ DO3A with respect to DMAE ‐ DO3A (i.e., log K_{Gd‐ AE‐DO3A} =22.40 and log K_{Gd‐ DMAE‐DO3A} =20.56). The transmetallation reactions of Gd^III complexes are very slow (Gd‐ AE ‐ DO3A : t_1/2=2.7×10⁴ h; Gd‐ DMAE ‐ DO3A : 1.1×10⁵ h at pH 7.4 and 298 K) and occur through proton‐assisted dissociation.     

Periodical bubble formation and the oscillatory change in dissolved oxygen concentration in a catalase-hydrogen peroxide system.

The relationship between the periodical bubble forming and the oscillatory change in the dissolved oxygen (DO) concentration in a catalase-hydrogen peroxide system was studied. Photographs of the bubbles and the responses from the DO electrode indicated that large bubbles were generated periodically, and that the DO profile depended on the geometrical relationship between the electrode and the bubbles.     

Determination of dissolved oxygen by catalytic reduction on Nafion-methyl viologen chemically modified electrode

A small size Nafion-methyl viologen chemically modified electrode (Nafion-MV CME) together with a small size electrolytic cell were constructed for the purpose of dissolved oxygen (DO) determination. The catalytic reduction of DO on Nafion-MV CME results in fast and sensitive DO determination. The mechanism of such detection is also considered.     

A simple and rapid method for measuring dissolved oxygen in waters with gold microelectrode

Dissolved oxygen (DO) is an essential indicator in chemical, biological and biochemical processes and needs to be rapidly measured in many cases. In this work, a rapid, sensitive and simple electrochemical method, first derivative linear sweep voltammetry (FD-LSV), was established for the determination of DO. The peak height of FD-LSV was found to be influenced by scan rate and microelectrode surface area. An empirical formula was proposed to describe the relationship between the FD-LSV peak height and the influencing factors. Compared with other electrochemical methods for DO determination, the FD-LSV method needed lesser time and was more accurate. This method was successfully applied for the determination of the DO levels of various environmental water samples.     

水质COD、DO测试结果可信度的未确知数分析方法

水质COD、DO测试易受各种主、客观因素影响，其测试结果是一具有可信度的未确知数。为确保测试结果能正确反映所测COD、DO实际情况，进行测试结果的可信度分析显得尤为重要；为此，本文将未确知数理论运算应用于水质COD、DO测试结果的可信度分析，以确保测试结果的可靠性。经理论分析和实际测试表明，该法较好地评判水中COD、DO测试结果以及相应于结果的可信度，可推广应用于水质分析。