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981.
982.
Melanie Aubert Ronan C. Nicolas Weronika Pawelec Carl‐Eric Wilén Michael Roth Rudolf Pfaendner 《先进技术聚合物》2011,22(11):1529-1538
A number of symmetrical and unsymmetrical azoalkanes of the general formula R′?N = N?R and related azoxy, hydrazone as well as azine derivatives have been synthesized in order to assess their potential as novel flame retardants for polypropylene alone or in combination with commercially available flame retardants such as alumina trihydrate (ATH), decabromodiphenyl ether (DecaBDE) and tris(3‐bromo‐2,2‐bis(bromomethyl)‐propyl)phosphate (TBBPP). The experimental results show that in the series of different sized azocycloalkanes the flame retardant efficacy decreased in the following order: R = cyclohexyl > cyclopentyl > cyclobutyl > cyclooctanyl >> cyclododecanyl. Whereas in the series of aliphatic azoalkanes compounds the efficacy decreased in the following order: R = n‐alkyl > tert‐butyl > tert‐octyl. In addition, also some of the prepared azoxy, azine, and hydrazone derivatives provide flame retardancy to polypropylene films at already very low concentrations (0.25–1 wt%). Noteworthy is that in contrast to other halogen‐free radical generators, the azoalkanes are also very effective as flame retardants in polypropylene thick moldings. Interestingly, it was found that 4,4′‐bis(cyclohexylazocyclohexyl)‐methane) shows a strong synergistic effect with ATH. Thus, in the presence of 0.5 wt% of azoalkane the ATH loading could be reduced from 60 to 25 wt% and still UL94 V‐2 rating could be reached. Furthermore, the fire testing data reveal that azoalkanes show a synergistic effect with DecaBDE and when used in conjunction with very low loadings of TBBPP. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
983.
《Optimization》2012,61(3-4):325-338
Asymptotic properties of reachable sets of singularly perturbed differential inclusions are given. Their applications to optimal control problems are also studied 相似文献
984.
Pol Besenius 《Journal of polymer science. Part A, Polymer chemistry》2017,55(1):34-78
The self‐assembly into supramolecular polymers is a process driven by reversible non‐covalent interactions between monomers, and gives access to materials applications incorporating mechanical, biological, optical or electronic functionalities. Compared to the achievements in precision polymer synthesis via living and controlled covalent polymerization processes, supramolecular chemists have only just learned how to developed strategies that allow similar control over polymer length, (co)monomer sequence and morphology (random, alternating or blocked ordering). This highlight article discusses the unique opportunities that arise when coassembling multicomponent supramolecular polymers, and focusses on four strategies in order to control the polymer architecture, size, stability and its stimuli‐responsive properties: (1) end‐capping of supramolecular polymers, (2) biomimetic templated polymerization, (3) controlled selectivity and reactivity in supramolecular copolymerization, and (4) living supramolecular polymerization. In contrast to the traditional focus on equilibrium systems, our emphasis is also on the manipulation of self‐assembly kinetics of synthetic supramolecular systems. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 34–78 相似文献
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987.
为了实现对基于自由摆的平板的控制,建立了基于自由摆的平板控制系统.首先分析平板的控制转角与自由摆转角的关系,推导出关系式,再对控制单元、反馈单元进行分析比较给出方案,采用32位LPC2138(ARM7)处理器为平板控制系统的中央控制单元,实现由高精度电位器测量出摆动角度后由步进电机控制的平板在周期摆动中做相应反馈调整,然后在现有器件的基础上编制出控制软件,在设备上进行调试,最后对系统的精度进行分析并进行实际测量.测量结果表明激光笔在摆动中照射在靶板上的光斑偏离基准线最大0.89cm,基本满足对平板的控制要求. 相似文献
988.
采用TiO2上高度分散的金纳米粒子做催化剂,从脂肪族硝基化合物、醛和氢气可高选择性合成硝酮。与碳负载Pt催化剂相比,该催化体系上硝酮的选择性从50%增加到90%。其催化性能可有活性位结构、载体特性和反应条件精确调节。 相似文献
989.
Blue luminescent compounds T1-T4 containing triphenylamine donors,bipyridine acceptors and olefinic linkers were synthesized and characterized by 1H NMR,13C NMR and high resolution mass spectrometry(HR... 相似文献
990.