反对数微分简易示波伏安法的研究

在获得微分简易地波伏安图的实验线路中,增加了反对数装置,提出了反对数微分简易示波伏安法。该方法被应用于铝合金中微量铜和分子筛中微量钴的测定,获得了满意结果。     

Thiazolium-mediated multicomponent reactions: a facile synthesis of 3-aminofuran derivatives

[reaction: see text] A facile synthesis of highly functionalized 3-aminofuran derivatives by the multicomponent reactions of thiazolium salts, aldehydes, and DMAD is described.     

SYNTHESIS AND POLYMERIZATION OF ALIPHATIC TERTIARY AMINO-GROUP N-SUBSTITUTED ACRYLAMIDES

Aliphatic tertiary amino-group N-substituted acrylamides, N-acryl-N′-methylpiperazine (AMP)and N-methacryl-N′-methylpiperazine (MAMP) were synthesized directly from N-methylpiperazinewith corresponding acryloyl chlorides and characterized by elementary analysis of their picrates,~1H-NMR, IR and MS. AMP did not polymerize with benzoyl peroxide (BPO), but could poly-merize with lauroyl peroxide (LPO). The rate equation of the polymerization was given as R_P=K_P [AMP]~(1.5)[LPO]~(0.5) and the overall activation energy of this polymerization system was 10.8Kcal/mol. The redox nature of LPO with the monomer itself was suggested. Even though AMP and MAMP hardly proceed the polymerization initiated with BPO, butunder lower concentration would form redox system with BPO to initiate the polymerization of MMAreadily. The rate equation of the polymerization of MMA initiated with MAMP-BPO systemwas given as R_P=K_P [MMA] [MAMP}~(0.5) [BPO]~(0.5) and the overall activation energy was 10.2Kcal/mol. The analysis of the obtained polymers confirmed that MAMP not only initiated the poly-merization of MMA by combining with BPO, but also took part in the polymer chains impartingthem with better biocompatibility.     

Nonlinear vibration isolation via an innovative active bionic variable stiffness adapter (ABVSA)

Nonlinear Dynamics - During the process of spacecraft launch, the extreme vibration environment is the major influence factor that induces the failure of the mission. Inspired by the smooth motions...     

微分简易示波伏安法测定分子筛中微量钴的研究

微分简易示波伏安法是一种新的示波分析方法．与经典示波计时电位法相比，具有灵敏度高、去极剂峰高易于测定等优点．本文研究了CO－4（2一毗院偶氮）间苯二酚钠（PAR）体系的示波特性并探讨了应用微分简易示波伏安法测定微量钻的可能性．试验发现，在O．2mol／LHAc－0·2mol／LNaAc－2·5X10－’mol／LPAR底液中，钻离子在iFE曲线的阴极支上电位为一1．68V处产生一尖锐峰，其峰高与钻离子浓度在1．5X10’～1·2X10－‘mol／L范围内呈线性关系，检测灵敏度为5．OXIO－’mol／L‘以此拟定了测定微量钻的新方法．与光度法相比，该…     

343 nm飞秒激光制备微孔阵列以增强聚氨酯合成革透湿性

为了提高聚氨酯(PU)合成革透湿性,分别使用343 nm飞秒激光和作为对比的1030 nm飞秒激光及1064 nm纳秒激光制备微孔阵列。采用扫描电镜(SEM)和3D激光扫描显微镜对比研究了微孔形貌。结果表明,343 nm飞秒激光可以制备出效果最佳的微孔。此外,分析了3种激光与PU涂层的作用机理,揭示了343 nm飞秒激光合成革微钻孔过程仅表现为光化学烧蚀,光化学和光热烧蚀同时发生于1030 nm飞秒激光钻孔过程,而1064 nm纳秒激光只显示了光热烧蚀。激光合成革表面钻孔后,测量其透湿性和抗张力。结果显示: 微孔密度越大,皮革透湿性(WVP)越大而抗张力越低,脉冲重叠的增加会导致WVP的增加和抗张力的下降;同时,随着脉冲重叠从91.7%降到50%,微孔直径从45 μm降低到30 μm,而微孔锥度从0.7°增加到12.1°;当脉冲重叠率为91.7%,微孔密度为2550/cm²时,最大的WVP增长率为306%。     

Piperidine Nucleophilic Substitution Without Solvent: An Efficient Synthesis of Raloxifene

Mild and high-yielding synthesis is described for raloxifene via piperdine nucleophilic substitution of a new raloxifene intermediate 3-aroyl-2-aryl-substituted benzo[b]thiophenes, which is obtained by acylation of para-substituted benzoyl chlorides and 2-arylbenzo[b]thiophenes. The key step is solvent free and offers valuable advantages, such as low cost, and is suitable for industrial production.     

Acylation of alkylidenecyclopropanes for the facile synthesis of alpha,beta-unsaturated ketone and benzofulvene derivatives with high stereoselectivity

[reaction: see text] A variety of substituted alpha,beta-unsaturated ketone and benzofulvene derivatives were readily prepared in good to excellent yields via the reaction of alkylidenecyclopropanes with various acyl chlorides in the presence of aluminum chloride. The stereochemistry of the acylation and cyclization is discussed.     

A Supersonic Aerodynamic Energy Harvester:A Functionally Graded Material Beam with a Giant Magnetostrictive Thin Film

In this study,a simply supported functionally graded material beam with a giant magnetostrictive thin film(GMF)was selected as an energy harvester.Based on the ...     

Palladium-Catalyzed Dehalogenation of Benzofuran Bromides

Various benzofuran bromides were dehalogenated using the palladium catalyst and phosphine ligands in the present of 5 equiv water. This set up a new and efficient protocol for the palladium-catalyzed dehalogenation of benzofuran bromides, which could tolerate the presence of water and have selective debromination.