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排序方式: 共有87条查询结果,搜索用时 15 毫秒
1.
Moira Chas 《Topology》2004,43(3):543-568
Goldman (Invent. Math. 85(2) (1986) 263) and Turaev (Ann. Sci. Ecole Norm. Sup. (4) 24 (6) (1991) 635) found a Lie bialgebra structure on the vector space generated by non-trivial free homotopy classes of curves on a surface. When the surface has non-empty boundary, this vector space has a basis of cyclic reduced words in the generators of the fundamental group and their inverses. We give a combinatorial algorithm to compute this Lie bialgebra on this vector space of cyclic words. Using this presentation, we prove a variant of Goldman's result relating the bracket to disjointness of curve representatives when one of the classes is simple. We exhibit some examples we found by programming the algorithm which answer negatively Turaev's question about the characterization of simple curves in terms of the cobracket. Further computations suggest an alternative characterization of simple curves in terms of the bracket of a curve and its inverse. Turaev's question is still open in genus zero. 相似文献
2.
Oriented closed curves on an orientable surface with boundary are described up to continuous deformation by reduced cyclic
words in the generators of the fundamental group and their inverses. By self-intersection number one means the minimum number
of transversal self-intersection points of representatives of the class. We prove that if a class is chosen at random from
among all classes of m letters, then for large m the distribution of the self-intersection number approaches the Gaussian distribution. The theorem was strongly suggested
by a computer experiment with four million curves producing a very nearly Gaussian distribution. 相似文献
3.
This paper describes simple methods of demonstrating macroscale spontaneous assembly. These demonstrations can illustrate topics in college or high school chemistry courses, such as the thermodynamics of crystallization and the chelate effect. The assembling units are built from a combination of magnetic and conventional LEGO building blocks. Unlike many other spontaneous-assembly experiments, these assemblies do not require surface flotation to form. 相似文献
4.
5.
Chas Lüdeking 《Fresenius' Journal of Analytical Chemistry》1890,29(1):342
Ohne Zusammenfassung 相似文献
6.
Holborn und Chas P. McKenna 《Fresenius' Journal of Analytical Chemistry》1904,43(10):639-640
Ohne Zusammenfassung 相似文献
7.
The structure elucidation of a novel natural product pavettamine (1), the causal agent of the plant toxicosis gousiekte, is reported. The structure was defined by analysis of NMR and MS data and the relative configuration followed from the 13C NMR data of the acetonide derivative. The absolute stereochemistry was established by total synthesis from (2S)-malic acid using chiral sulfoxide methodology as (2S,4R,8R,10S)-1,11-diamino-6-aza-undecane-2,4,8,10-tetraol. 相似文献
8.
Wolfgang Denzer Gus Hancock John C Pinot de Moira Phillip L Tyley 《Chemical physics letters》1997,280(5-6)
Time-of-flight measurements have been made of the O(1D) fragment following the photolysis of ozone in the near-UV. At 321.9 nm fragments are seen with kinetic energies the values of which are those expected from spin-forbidden dissociation with ground state O2(X3Σg−) molecules as the co-product. Spin-allowed dissociation of internally excited ozone molecules is also seen to produce translationally cold O(1D) and O2(a1Δg) products. The implications for the dissociation of tropospheric ozone are briefly discussed. 相似文献
9.
Gan Q Zou Y Rooney D Nancarrow P Thompson J Liang L Lewis M 《Advances in colloid and interface science》2011,164(1-2):45-55
Supported ionic liquid membranes (SILMs) has the potential to be a new technological platform for gas/organic vapour separation because of the unique non-volatile nature and discriminating gas dissolution properties of room temperature ionic liquids (ILs). This work starts with an examination of gas dissolution and transport properties in bulk imidazulium cation based ionic liquids [C(n)mim][NTf2] (n=2.4, 6, 8.10) from simple gas H(2), N(2), to polar CO(2), and C(2)H(6), leading to a further analysis of how gas dissolution and diffusion are influenced by molecular specific gas-SILMs interactions, reflected by differences in gas dissolution enthalpy and entropy. These effects were elucidated again during gas permeation studies by examining how changes in these properties and molecular specific interactions work together to cause deviations from conventional solution-diffusion theory and their impact on some remarkably contrasting gas perm-selectivity performance. The experimental perm-selectivity for all tested gases showed varied and contrasting deviation from the solution-diffusion, depending on specific gas-IL combinations. It transpires permeation for simpler non-polar gases (H(2), N(2)) is diffusion controlled, but strong molecular specific gas-ILs interactions led to a different permeation and selectivity performance for C(2)H(6) and CO(2). With exothermic dissolution enthalpy and large order disruptive entropy, C(2)H(6) displayed the fastest permeation rate at increased gas phase pressure in spite of its smallest diffusivity among the tested gases. The C(2)H(6) gas molecules "peg" on the side alkyl chain on the imidazulium cation at low concentration, and are well dispersed in the ionic liquids phase at high concentration. On the other hand strong CO(2)-ILs affinity resulted in a more prolonged "residence time" for the gas molecule, typified by reversed CO(2)/N(2) selectivity and slowest CO(2) transport despite CO(2) possess the highest solubility and comparable diffusivity in the ionic liquids. The unique transport and dissolution behaviour of CO(2) are further exploited by examining the residing state of CO(2) molecules in the ionic liquid phase, which leads to a hypothesis of a condensing and holding capacity of ILs towards CO(2), which provide an explanation to slower CO(2) transport through the SILMs. The pressure related exponential increase in permeations rate is also analysed which suggests a typical concentration dependent diffusion rate at high gas concentration under increased gas feed pressure. Finally the strong influence of discriminating and molecular specific gas-ILs interactions on gas perm-selectivity performance points to future specific design of ionic liquids for targeted gas separations. 相似文献
10.
Senthilkumar Sivaprakasam Moira Monika Schuler Adel Hama Katie-Marie Hughes Ian W. Marison 《Journal of Thermal Analysis and Calorimetry》2011,104(1):75-85
Control of bioprocesses requires reliable and robust on- or in-line monitoring tools providing real-time information on process
dynamics. Heat generation related to metabolic activity of living systems is currently gaining importance in bioprocess industry
due to its non-invasive and essentially instantaneous characteristics. This study deals with monitoring and control of pure
aerobic fed-batch cultures of three Crabtree-negative yeast strains, Kluyveromyces marxianus, Candida utilis and Pichia pastoris, based on in-line measured, metabolic heat flow signals. A high resolution biocalorimeter (BioRC1) was developed from a standard
bench-scale heat flow calorimeter (RC1). The BioRC1 was equipped with in-line (dielectric spectroscopy, pH probe and dissolved
oxygen probe) and at-line (exit gas analyser) sensors to characterise the growth behaviour of the yeast cells. Both metabolic
heat flow and biomass profiles exhibited similar behaviour proving the significance of employing heat flow signal as a key-parameter
for the system under investigation. A simple estimator for biomass concentration and specific growth rate was formulated based
on heat flow values. In order to evaluate the potential of calorimetry as a reliable and powerful process monitoring tool,
the robustness, reliability as well as the broad applicability of the developed estimators was assessed through comparison
with off-line measurement techniques and showed promising results for general applicability with a wide range of bioprocesses. 相似文献