Preparation and characterization of novel hyperbranched poly(amido amine)s from Michael addition polymerizations of trifunctional amines with diacrylamides

Novel hyperbranched poly(amido amine)s containing tertiary amines in the backbones and acryl as terminal groups were synthesized via the Michael addition polymerizations of trifunctional amines with twofold molar diacrylamide. The hyperbranched structures of these poly(amido amine)s were verified by ¹³C NMR (INVGATE). The polymerization mechanisms were clarified by following the polymerization process with NMR method, and the results show that the reactivity of secondary amine formed in situ is much lower than that of the secondary amine in 1‐(2‐aminoethyl) piperazine (AEPZ) ring and the primary amine. The secondary amine formed in situ was almost kept out of the reaction before the primary and secondary amines in AEPZ were consumed, leading to the formation of the AB2 intermediate, and the further reaction of the AB2 yielded the hyperbranched polymers. The molecular weights and properties of poly(amindo amine)s obtained were characterized by GPC, DSC, and TGA, respectively. Based on the reaction of active acryl groups in the polymers obtained with glucosamine, hyperbranched polymers containing sugar were formed. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5127–5137, 2005     

POLYNOMIAL SOLUTIONS TO PIEZOELECTRIC BEAMS (Ⅰ)——SEVERAL EXACT SOLUTIONS

IntroductionDue to its excellent piezoelectric properties,composites made of piezoelectric materialsare found widespread applications and attracted more attentions[1-10].Because of materialanisotropy and couplingbetween mechanical deformation and electric…     

Model filled polymers. IX. Synthesis of uniformly crosslinked polystyrene microbeads

Monodisperse sized crosslinked polystyrene (PS) beads prepared by reaction of styrene (S) and divinylbenzene (DVB), in batch emulsion copolymerization in the absence of emulsifiers, are not uniformly crosslinked, because DVB is more reactive than S. For copolymerization of 1 to 10 mol % DVB and S, within each crosslinked PS microbead, the crosslink density varies by a factor exceeding two and decreases with increased conversion. A semicontinuous copolymerization, involving incremental additions of DVB, produces uniformly crosslinked PS beads. For both copolymerization techniques, T_g correlates well with crosslink density and PS beads are spherical and monodisperse in size. © 1992 John Wiley & Sons, Inc.     

双狭缝透射光栅软X光时空分辨谱仪

 利用双狭缝、透射光栅配亚仟X光条纹相机做了具有一维空间、时间和能谱分辨的三维软X光测量仪器(双狭缝透射光栅软X光时空分辨谱仪), 并成功地获得了金盘靶的N带X光(中心波长1.7nm)时空分辨图象 。该仪器空间分辨可达23μm, 时间分辨可达003ns, 能谱分辨(当源大小为100～300μm时对波长1.7nm的X光)可达0.4～ 0.7nm, 只需稍加改动, 即可用于其它波段的X光测量。     

吸附式空调系统的原理及添加剂强化吸附工质性能的研究

氯化锂晶体具有很高的吸水性能，在吸附式空调制冷系统中常常被用作吸附剂。本文介绍了吸附式空调制冷系统的原理，研究了吸附剂（氯化锂）、吸附质（水汽）的性质；采用高真空吸附重量法测定氯化锂的等温吸附曲线及氯化锂吸附水汽的速率，并通过添加一种既有吸附增稠作用，又能强化氯化锂吸附性能的添加剂,改善氯化锂的等温吸附特性,降低氯化锂的再生温度。采用氯化锂混合吸附剂-水的开式旋转吸附式空调系统，具有显著的节能效果和双重杀菌功能，提供人们所喜爱的舒适空调域（室内温湿度26．7℃／50%RH），同时改善室内空气品质。     

大平面二极管虚阴极振荡器的宽脉冲微波辐射

给出了产生宽脉冲微波辐射的大平面天鹅绒二极管虚阴极振荡器的结构和测试装置，测得了二极管中阴－阳极等离子体的闭合速率为３０～４３ｋｍ／ｓ，获得了微波辐射的最大脉宽为１．５μｓ，产生的微波峰值功率约为１５ＭＷ，频率为０．５ＧＨＺ，指出这种平面二极管型虚阴极振荡器在辐射脉宽，辐射频率和辐射功率三者之间存在着物理上的制约关系，认为同轴型虚阴极振荡器是突破这种制约关系的一个新途径．     

H—空间的覆盖性质及其应用

我们得到了Ｈ－空间闭（开）覆盖性质的几个定理，改进和推广了Ｓｐｅｒｎｅｒ，Ｋｌｅｅ，Ａｌｅｘａｎｄｒｏｆｆ－Ｐａｓｙｎｋｏｆｆ，Ｂｅｒｇｅ，Ｇｈｏｕｉｌａ－Ｈｏｕｒｉ，Ｄａｎｚｅｒ－Ｇｒｕｎｂａｕｍ－Ｋｌｅｅ，Ｋｙ Ｆａｎ，ｓｈｉｈ－Ｔａｎ，Ｈｏｒｖａｔｈ和Ｌａｓｓｏｎｄｅ等人的相应结果。作为应用，我们对ｌ．ｃ．－空间内的下半连续集值映象证明了一个几站不动点定理并且推广吉洪诺夫不动点定理到ｌ．ｃ．     

Determination of Herbicide Residues in Garlic by GC–MS

A rapid multi-residue method has been developed for the determination of 16 herbicides in garlic. The analytical procedure is based on prior microwave heating prevention of the generation of sulfur-containing compounds. The garlic samples which had been pretreated were extracted with acetonitrile and cleaned up by solid-phase extraction. The herbicide residues were detected by gas chromatography–mass spectrometry with selected ion monitoring. The recoveries of 16 herbicides ranged from 69.0 to 105.4% with the relative standard deviations (RSD) below 10.1%. The limit of quantification (LOQ) ranged from 0.003 to 0.015 mg kg^?1.     

Liquid-liquid extraction of protactinium(V) using tri-iso-octylamine

Solvent extraction of protactinium with tri-iso-octyl-amine (TIOA) in xylene, benzene, carbon tetrachloride and chloroform from HCl, HF, HNO₃, HClO₄ and H₂SO₄ media was studied using ²³³Pa as a radiotracer. The extraction efficiencies of protactinium were determined as a function of shaking time, concentrations of mineral acids in aqueous phase, extractant concentrations and diluents in organic phase. The extraction mechanism was discussed. The results show that the extracted species in the organic phase is [(R₃N⁻H)_nPa(OH)_xCl _y ^5−x−y ].