The Synthesis of Covalent Triazine-Based Frameworks via Friedel–Crafts Reactions of Cyanuric Chloride with Thienyl and Carbazolyl Derivatives for Fluorescence Sensing to Picric Acid,Iodine and Capturing Iodine

A multifunctional thiophene-based covalent triazine framework (TTPATTh) with triphenylamine as core is synthesized by Friedel–Crafts reaction of cyanuric chloride with thienyl derivative for the first time. The yield of TTPATTh (99.59%) is far higher than that of the carbazole-based CTF (TTPATCz, 47.03%). TTPATTh and TTPATCz possess high BET surface areas with 1235 and 2501 m² g^–1 as well as high pore volumes with 1.60 and 2.23 cm³ g^–1, respectively. TTPATTh and TTPATCz have high thermal stability with high thermal decomposition temperatures of 514 and 598 °C in nitrogen atmosphere. With the introduction of triazine rings, the fluorescence sensing sensitivities of TTPATTh and TTPATCz to picric acid and iodine are improved significantly. Especially for TTPATTh, the K_sv values reach 5.95 × 10⁵ and 1.61 × 10⁴ L mol^–1, and LODs reach 1.02 × 10^–12 and 1.86 × 10^–12 mol L^–1. To the best of the knowledge, this is the most sensitive value among thiophene-based porous organic polymers to PA and I₂. Furthermore, TTPATTh and TTPATCz can also adsorb iodine in vapor phase, cyclohexane solution and aqueous solution, and release iodine by heating or in ethanol solution. The efficiency of controlling the release of iodine is higher than that in ethanol.     

稀土含量对喷熔层组织及耐蚀性的影响

本文通过在镍基自熔合金粉末中加入不同含量的稀土，研究了稀土含量对喷熔层组织及耐蚀性的影响规律及其作用机制。结果表明，在喷熔材料中加入适量稀土，可使喷熔层组织细化、晶界净化，从而使腐蚀过程中的表面活性点减少，耐蚀性提高。     

汽车后市场准入门槛亟需设防

任何市场都是有规则的,没有标准的市场是短暂的.经销商要有一个好的经营环境,必须把这个门槛设好. 汽车后市场还需要准入门槛? 李庆云现任天津环渤海汽车城董事长并身兼天津市交易市场协会会长,在没有跨进汽车行业之前,一直觉得这样的问题多余:哪个行业没有准入门槛?等自己在天津建立环渤海汽车城之后,才意识到,中国的汽车后市场是多么需要"设防".     

Properties of poly(n‐butyl methacrylate) prepared by reverse atom transfer radical polymerization in an aqueous dispersed system

Reverse atom transfer radical polymerization (ATRP) of n‐butyl methacrylate (BMA) in waterborne media using Cu(II) complexes with azo initiators (i.e., reverse ATRP) was conducted. The influence of several factors, such as surfactant, catalyst, and reaction time, on the stability of the emulsion, the particle size, the morphology of the emulsion particles, and the control of the polymerization was investigated. The results showed great differences between ATRP and conventional emulsion polymerization, especially the nucleation mechanism and the kinetics. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1542–1547, 2003     

碱土金属在萃取剂与树脂间反应平衡常数的测定

研究了碱土金属离子在Ｄ００１树脂与８－羟基喹啉三氯甲烷溶液间的平衡常数Ｏ－ｔＫ的测定。其值依Ｍｇ、Ｃａ、Ｓｒ、Ｂａ次序减小。并得出萃取剂浓度［ＨＡ］。与金属离子在两相分配的关系。     

氯化聚丙烯改性胶粘剂的合成及粘附性能研究

以甲苯为溶剂，过氧化二苯甲酰(BP0)为引发剂，通过自由基聚合，采用甲基丙烯酸羟乙酯(HEMA)和苯乙烯(St)接枝改性氯化聚丙烯(CPP)。研究了不同苯乙烯用量、不同反应温度、不同反应时间、不同引发剂用量对改性氯化聚丙烯胶粘剂粘附性能的影响，得出较佳的工艺条件为反应温度90℃，反应时问2h，原料配比m(CPP)：m(HEMA)：m(St)：m(BPO)=50：0．5：0．6：0．15。     

PVA-based activated carbon fibers with lotus root-like axially porous structure

A novel method was developed for the fabrication of activated carbon fiber (ACF) with wet spinning polyvinyl alcohol (PVA) fibers as the precursors. Through a combination of preoxidation, dehydration, carbonization and activation under a certain tension, PVA-based ACFs (PVA-ACFs) with high yields and good mechanical properties were obtained. The surface and cross-section morphologies, pore structures, surface geometries, surface functional groups and crystal structures of the PVA-ACFs were characterized using field emission scanning electron microscopy, low temperature nitrogen adsorption, Fourier transformed infrared spectrophotometry, X-ray photoelectron spectroscopy and X-ray power diffraction. All the PVA-ACF samples prepared had lotus root-like axially meso- and macroporous structures with the domination of micropores. Fractal geometries of PVA-ACFs deduced from nitrogen adsorption isotherms indicates that capillary force dominated in the interactions between nitrogen and the PVA-ACFs. The surface functional groups of the PVA-ACFs depend on the activating agents. Graphitoidal crystal structures were observed for the PVA-ACFs. The small crystal size and short range ordering between the crystallites ensured a high specific surface area of the PVA-ACFs.     

Effect of Product Conductivity on Field-Activated Combustion Synthesis

Experimental and modeling results on the field-activated combustion synthesis (FACS) of Nb₅Si₃ are reported. In the absence of an electric field and without reactant preheating, Nb₅Si₃ cannot be prepared by self-propagating high-temperature synthesis (SHS). Under the influence of a field a self-sustaining combustion wave is established whose rate of propagation decreases with traveled distance. For relatively low field values, the wave propagation mode changes from a continuous (smooth) to a spin mode. The product of synthesis depends on the mode of propagation. Synthesis during continuous wave propagation results in the formation of Nb₅Si₃, primarily in the α-modification. In contrast, when the wave propagates in a spin mode, the product is NbSi₂ with unreacted niobium. The present observations demonstrate a case where the field effect is not localized, as was the case in previous studies. The difference in behavior is attributed to differences in the electrical conductivities of the product phases.     

新型层状表面相锆基固体酸催化酯化反应研究

将所研制的层状表面相锆基固体酸催化剂用于一元、二元醇醋酸酯和其他羧酸酯类产品的合成 ,考察了其催化性能。研究发现 :层状表面相锆基固体酸催化剂对所考察的酯化反应具有很好的普遍适用性 ,但其酯化率与醇的性质和结构密切有关。催化反应动力学研究表明乙酸与丁醇、戊醇、己醇的酯化反应均为二级反应 ,且反应活化能均较低 ,分别为 47 4kJ/mol、2 3 3kJ/mol和 19 8kJ/mo     

Cu2O/Cu Cermet as a Candidate Inert Anode for Al Production

Cu₂O/ x Cu ( x =0–25 wt%) cermets were evaluated as a novel partially inert anode for aluminum (Al) production. The physical and mechanical properties, including the compressive strength, flexural strength, thermal expansion coefficient, thermal conductivity, and dc electrical conductivity were tested at room temperature and at temperatures up to 950°C. The coefficient of thermal expansion, compressive strength, flexural strength, thermal conductivity, and electrical conductivity of Cu₂O/Cu cermets increased with increasing Cu content. High-temperature electrical conductivity measurements showed that with increasing temperature, the electrical conductivity increased when the Cu content was below the percolation threshold, while it decreased when the Cu content was above the percolation threshold. A relatively stable CuAlO₂ layer formed on the cermet surface during electrochemical testing, and the corrosion rate of this anode was estimated to be about 1.8–1.9 cm/year in Al production.