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Dr. Sofia Curland Dr. Christoph Allolio Leah Javitt Shiri Dishon Ben-Ami Dr. Isabelle Weissbuch Dr. David Ehre Prof. Dr. Daniel Harries Prof. Dr. Meir Lahav Prof. Dr. Igor Lubomirsky 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(36):15705-15709
Electrofreezing experiments of super-cooled water (SCW) with different ions, performed directly on the charged hemihedral faces of pyroelectric LiTaO3 and AgI crystals, in the presence and in the absence of pyroelectric charge are reported. It is demonstrated that bicarbonate (HCO3−) ions elevate the icing temperature near the positively charged faces. In contrast, the hydronium (H3O+) slightly reduces the icing temperature. Molecular dynamics simulations suggest that the hydrated trigonal planar HCO3− ions self-assemble with water molecules near the surface of the AgI crystal as clusters of slightly different configuration from those of the ice-like hexagons. These clusters, however, have a tendency to serve as embryonic nuclei for ice crystallization. Consequently, we predicted and experimentally confirmed that the trigonal planar ions of NO3− and guanidinium (Gdm+), at appropriate concentrations, elevate the icing temperature near the positive and negative charged surfaces, respectively. On the other hand, the Cl− and SO42− ions of different configurations reduce the icing temperature. 相似文献
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C. Harries 《Fresenius' Journal of Analytical Chemistry》1916,55(7):352-353
Ohne Zusammenfassung 相似文献
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Dan Ben-Yaakov David Andelman Rudi Podgornik Daniel Harries 《Current Opinion in Colloid & Interface Science》2011,16(6):542-550
In aqueous solutions, dissolved ions interact strongly with the surrounding water and surfaces, thereby modifying solution properties in an ion-specific manner. These ion-hydration interactions can be accounted for theoretically on a mean-field level by including phenomenological terms in the free energy that correspond to the most dominant ion-specific interactions. Minimizing this free energy leads to modified Poisson-Boltzmann equations with appropriate boundary conditions. Here, we review how this strategy has been used to predict some of the ways ion-specific effects can modify the forces acting within and between charged interfaces immersed in salt solutions. 相似文献
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This is the second of two papers exploring children’s responses to an extended version of a division-with-remainder problem intended to elicit general rather than particular realistic considerations during mathematical problem solving. Responses to two problems are analyzed. The first is a ‘realistically’ contextualised item drawn from national tests in England whose ambiguities have been previously discussed (Cooper, 1992); the second is a version of this problem revised to encourage a wider range of realistic responses. In Cooper and Harries (2002), the responses of children at the end of their first year of secondary schooling were analyzed. Here the responses of children at the end of their primary schooling are analyzed and compared with the previous results. It is shown that many children, given suitable encouragement, are willing and able to enter into an extended form of realistic thinking during problem solving, although the original test item renders this invisible. 相似文献
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T. Tanaka M. Hoshino H. Kato J.R. Harries Y. Tamenori K. Ueda H. Tanaka 《Journal of Electron Spectroscopy and Related Phenomena》2008,164(1-3):24-27
We report soft X-ray total ion yield and angular-resolved ion yield spectra of CF3I in the C 1s, I 3d and F 1s ionisation regions, and tentatively assign the observed electronic states. Anisotropy in ion yield is observed only for the C transition, indicating that the dipole moment for this transition is parallel to the C3v. The effusive source of CF3I is heated to 800 K to produce a mixture of CF3 and I, and the resulting spectra are compared to those recorded at room temperature. 相似文献
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C. Harries 《Colloid and polymer science》1923,33(3):181-184
Zusammenfassung Es wird der Begriff Aggregation und Desaggregation erörtert. Die Aggregation entsteht durch gegenseitige Adsorption zweier oder mehrerer disperser Phasen. Die Aggregate lassen sich zu einfachen dispersen Phasen durch Peptisation desaggregieren. Die Polymerisate werden durch Peptisieren nicht depolymerisiert. Diese Erörterungen finden ihre Stütze in Beobachtungen, welche bei den Zustandsänderungen des Schellacks und des Kautschuks gemacht sind. 相似文献