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Ultrasonic guided waves (GWs) can be used to evaluate long bones effectively because of the ability to provide the information of the whole bone. In this study, a joint spectrogram segmentation and ridge-extraction (JSSRE) method was proposed to separate multiple modes in long bones. First, the Gabor time-frequency transform was applied to obtain the spectrogram of multimodal signals. Then, a multi-class image segmentation algorithm was used to find the corresponding region of each mode in the spectrogram, including an improved watershed transform and a region growing procedure. Finally, the ridges were extracted and the time domain signals representing individual modes were reconstructed from these ridges in each region. The validations of this method were discussed by simulated multimodal signals with different signal-to-noise ratios (SNR). The correlation coefficients between the original signals without noise and the reconstructed signals were calculated to analyze the results quantitatively. The results showed that the extracted ridges were in good agreement with generated theoretical dispersion curves, and the reconstructed signals were highly related to the original signals, even under the SNR=3 dB situation. 相似文献
64.
Daniel A Paterson Jordan P Abberley William TA Harrison John MD Storey 《Liquid crystals》2017,44(1):127-146
ABSTRACTThe synthesis and characterisation of several members of the 1,ω-bis(4-cyanobiphenyl-4′-yl) alkane (CBnCB) and the 1-(4-cyanobiphenyl-4′-yloxy)-ω-(4-cyanobiphenyl-4′-yl) alkane (CBnOCB) homologous series are reported. The new odd members described CB5CB, CB13CB, CB4OCB, CB8OCB and CB10OCB all exhibit twist-bend nematic and nematic phases. The members of these series already reported in literature, CB7CB, CB9CB, CB11CB and CB6OCB, were also prepared in order to allow for a direct comparison of their transitional properties. The properties of these dimers are also compared to those of the corresponding members of the 1,ω-bis(4-cyanobiphenyl-4,-yloxy) alkanes (CBOnOCB). For any given total spacer length, for odd members of these series, the nematic–isotropic transition temperatures and associated entropy changes are greatest for the CBOnOCB dimer and lowest for the CBnCB dimer. These trends are understood in terms of molecular shape. For short spacer lengths, the twist-bend nematic–nematic transition temperature (TNTBN) is higher for the CBnOCB series than for the CBnCB series but this is reversed as the spacer length increases. Of the CBOnOCB dimers, a virtual value of TNTBN was estimated for CBO3OCB and TNTBN was measured for CBO5OCB. These values are considerably lower than those observed for the corresponding members of the CBnCB or CBnOCB series. The dependence of TNTBN on molecular structure is discussed not only in terms of the molecular curvature but also in the ability of the molecules to pack efficiently. As the temperature range of the preceding nematic phase increases, so the twist-bend nematic–nematic transition entropy change decreases and the transition approaches second order for the longer spacers. For comparative purposes, the transitional behaviour of the even-membered dimers CB6CB, CB5OCB and CBO4OCB is reported and differences accounted for in terms of molecular shape. 相似文献
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DS Zhulai SA Bugaychuk GV Klimusheva TA Mirnaya VN Asaula VI Handziuk 《Liquid crystals》2017,44(8):1269-1276
The class of thermotropic ionic liquid crystals (LCs) of the metal alkanoates possesses a number of unique properties, such as intrinsic ionic conductivity, high dissolving ability and ability to form time-stable mesomorphic glasses. These ionic LCs can be used as nanoreactors for the synthesis and stabilisation of different types of nanoparticles (NPs). Thus, some semiconductors, metals and core/shell NPs were chemically synthesised in the thermotropic ionic liquid crystalline phase (smectic A) of the cadmium octanoate (CdC8) and of the cobalt octanoate (CoC8). By applying the scanning electron microscopy, the cadmium and cobalt octanoate composites containing CdS, Au, Ag and core/shell Au/CdS NPs have been studied. NPs’ sizes and dispersion distribution of the NPs’ size in the nanocomposites have been obtained. 相似文献
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基于催化应用调控氧化铈纳米材料的形貌 总被引:1,自引:0,他引:1
催化剂的设计、合成和结构调控是获得优异性能的关键.传统的策略主要是尽量减小催化剂颗粒尺寸以增加活性中心的数目,即尺寸效应.近年来,材料科学的快速发展使得在纳米尺度上调变催化剂的尺寸和形貌成为可能,特别是通过形貌调控可暴露更多的高活性晶面,大幅度提高催化性能,即纳米催化中的形貌效应.因此,调节催化剂的尺寸与形貌可以单独或协同优化材料的性能.氧化铈作为催化剂的重要组分与结构、电子促进剂被广泛应用于多相催化剂体系.本文总结了近期氧化铈材料形貌可控合成的进展,包括主要的合成策略和表征方法; 进而分析了氧化铈和金-氧化铈催化材料的形貌效应,指出金-氧化铈之间独特的相互作用与载体形貌密切相关; 阐述了氧化铈纳米材料因暴露晶面的差异而获得不同催化性能的化学机制. 相似文献
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Chen KF Lo SC Chang L Egerton R Kai JJ Lin JJ Chen FR 《Micron (Oxford, England : 1993)》2007,38(4):354-361
This paper demonstrates the applicability of electron-spectroscopic imaging (ESI) for valence-state mapping of the iron oxide system. We have previously developed a set of signal-processing methods for an ESI series, to allow mapping of sp(2)/sp(3) ratio, dielectric function and energy bandgap. In this study, these methods are applied to generate a valence-state map of an iron oxide thin film (Fe/alpha-Fe(2)O(3)). Two problems, data undersampling and a convolution effect associated with extraction of the image-spectrum from the core loss image series, were overcome by using cubic-polynomial interpolation and maximum-entropy deconvolution. As a result, the reconstructed image-spectrum obtained from the ESI series images has a quality as good as that of conventional electron energy-loss spectra. The L(3)/L(2) ratio of the reconstructed ESI spectrum is determined to be 3.30+/-0.30 and 5.0+/-0.30 for Fe and alpha-Fe(2)O(3), respectively. Our L(3)/L(2) ratio mapping shows an accurate correspondence across the Cu/Fe/alpha-Fe(2)O(3) region. The effect of delocalization and chromatic aberration on the ESI resolution is discussed and estimated to be about 2 nm for the case of L(3)/L(2) ratio mapping. 相似文献
69.
H. Schwiedessen G. Barth H. Müller-Neuglück A. C. Egerton F. L. Smith A. Becte Astapenja Wapnik Selkin E. Schulek G. Meyer W. L. Ghijsen Jr. L. W. Winkler M. H. Hey A. S. Smith J. B. Littlefield W. P. Yant L. B. Berger O. M. Faber R. Gros Kohn-Abrest T. E. Brehmer L. Sulima H. Tropsch W. J. Mattox R. H. Dalton R. P. Cowles C. Brambel A. H. Mc Kinney W. D. Turner 《Analytical and bioanalytical chemistry》1937,108(7-8):279-284
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