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John R. Ebdon Barry J. Hunt Paul Joseph Christopher S. Konkel Dennis Price Kelly Pyrah T. Richard Hull G. John Milnes Stephen B. Hill Christopher I. Lindsay John McCluskey Ian Robinson 《Polymer Degradation and Stability》2000,70(3):425-436
Methyl methacrylate (MMA) has been free radically copolymerized, both in bulk and in solution, with diethyl(methacryloyloxymethyl)phosphonate (DEMMP), to give polymers which are significantly flame retarded when compared with PMMA, as indicated by the results of limiting oxygen index (LOI) measurements, UL 94 tests, and the results of cone calorimetric experiments. The physical and mechanical properties of the copolymers are similar to those of PMMA, except that the bulk copolymers are slightly crosslinked, and are better than those of PMMA flame retarded to a similar extent by some phosphate and phosphonate additives. Examination of the some of the gaseous products of pyrolysis and combustion, and of chars produced on burning, show that flame retardation occurs in the copolymers by both a condensed-phase and a vapour-phase mechanism. The condensed-phase mechanism is shown to involve generation of phosphorus acid species followed by reaction of these with MMA units giving rise to methacrylic acid units. The methacrylic acid units subsequently form anhydride links, which probably impede depolymerization of the remaining MMA sequences, resulting in evolution of less MMA (the major fuel when MMA-based polymers burn). By undergoing decarboxylation, leading to interchain cyclisation and, eventually, to aromaticisation, the anhydride units are probably also the principal precursors to char. 相似文献
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Novel flame retardants containing cyclodextrin nanosponges and phosphorus compounds to enhance EVA combustion properties 总被引:1,自引:0,他引:1
Jenny Alongi Merima Poškovi? Francesco Trotta 《Polymer Degradation and Stability》2010,95(10):2093-2100
A novel flame retardant intumescent system, aimed to improve the fire stability of ethylene vinyl acetate copolymer (EVA), has been prepared by melt blending of the copolymer and a complex of cyclodextrin nanosponge-phosphorus compounds. As compared to traditional systems, this complex, stable in processing conditions, has the advantage that nanosponges act as both carbon sources and foam forming agents while the phosphorus compounds are able to directly generate phosphoric acid in situ. In this context, cyclodextrin nanosponges undergo dehydration in presence of the acid source, generating water vapour and char, and thus protecting the copolymer against combustion. Different acid sources have been investigated in order to reach the optimum interaction with the nanosponges. Raman measurements and thermogravimetric analyses have shown that the cavities of nanosponges entrapped the phosphorus derivatives forming stable complexes at the temperature of EVA processing. Different amounts of these complexes (5, 10 and 15 wt.%) have been added to EVA via melt blending and their flame retardancy properties measured by UL94 test and cone calorimetry. Strongly modified burning kinetics, as compared to the behaviour of the neat copolymer, have been found by UL94 test: V2 classification has been achieved for every formulation regardless of the type and the amount of complex used. EVA combustion behaviour by cone calorimetry has also been significantly affected: the heat release rate decreased dramatically down to ca. 20% in the presence of these new additives. 相似文献
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结合本台硬盘播控系统实际,阐述了模拟向数字过渡时期电视中心系统验收测试的方法,并对测试中的几点体会进行了介绍,最后还阐述了深入使用VM700T的一些方法。 相似文献
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设计了一种HART协议通信接口。给出了具体的软硬件设计,采用HART专业低功耗调制解调芯片AD5700实现了HART信号的调制、解调与载波监听,利用AD5421电流环数模转换器实现了4m A-20m A电流输出及变送器的二线制传输,达到了变送器与上位机进行HART远程通信的目的。 相似文献
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本文分析了美国手持式电动工具新老标准的变化,对今后一个时期电动工具企业的UL认证工作提出了建议. 相似文献
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Far-I.R. photoconductivity reveals the existence of at least four different kinds of SA1 acceptors in germanium quenched from T > 800 each acceptor producing two or more hydrogenic excitation line series. One acceptor is correlated with the presence of Ni, another one with strong Cu contamination. The two other acceptors, which we call ‘normal’ and ‘shifted’, occur in samples quenched without intentional doping. The experiments indicate that the SA1 acceptors in germanium are impurity complexes involving fast diffusing elements. We discuss a model according to which the SA1 acceptors would be interstitial-substitutional pairs of transition metals. In particular, we propose to assign the ‘normal’ SA1 acceptors to FeI-CuS pairs. 相似文献