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Rotem Shemesh Maksym Krepker Diana Goldman Yael Danin‐Poleg Yechezkel Kashi Nadav Nitzan Anita Vaxman Ester Segal 《先进技术聚合物》2015,26(1):110-116
Active antimicrobial packaging is a promising form of active packaging that can kill or inhibit microorganism growth in order to maintain product quality and safety. One of the most common approaches is based on the release of volatile antimicrobial agents from the packaging material such as essential oils. Due to their highly volatile nature, the challenge is to preserve the essential oils during the high‐temperature melt processing of the polymer, while maintaining high antimicrobial activity for a desired shelf life. This study suggests a new approach in order to achieve this goal. Antimicrobial active films are developed based on low‐density polyethylene (LDPE), organo‐modified montmorillonite clays (MMT) and carvacrol (used as an essential oil model). In order to minimize carvacrol loss throughout the polymer compounding, a pre‐compounding step is developed in which clay/carvacrol hybrids are produced. The hybrids exhibit a significant increase in the d‐spacing of clay and enhanced thermal stability. The resulting LDPE/(clay/carvacrol) films exhibit superior and prolonged antibacterial activity against Escherichia coli and Listeria innocua, while polymer compounded with pure carvacrol loses the antibacterial properties within days. The films also present an excellent antifungal activity against Alternaria alternata, used as a model plant pathogenic fungus. Furthermore, infrared spectroscopy analysis of the LDPE/(clay/carvacrol) system displayed significantly higher carvacrol content in the film as well as a slower out‐diffusion of the carvacrol molecules in comparison to LDPE/carvacrol films. Thus, these new films have a high potential for antimicrobial food packaging applications due to their long‐lasting and broad‐spectrum antimicrobial efficacy. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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Circular dichroism (CD) is frequently used to assess the secondary structure of peptides and proteins, whereas less attention has been given to their building blocks, that is, single amino acids, as they do not possess a secondary structure. Here, we follow the CD signal of amino acids and reveal that several acids exhibit a unique CD pattern as a function of their concentration. Accordingly, we propose an eight‐level classification of the CD signal of the various amino acids. Special focus is given to the CD pattern of phenylalanine (Phe), for which we observe the formation of an ultra‐narrow CD peak (full width at high maximum of only 5 nm). This CD peak can be attributed to the formation of Phe‐based chiral structural features. Further support for the formation of an ordered structure is given by using NMR, and the additional self‐assembly process of Phe to tubular structures. 相似文献
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Shahaf Nitzan Alexander Olevskii Alexander Ulanovskii 《Proceedings of the Steklov Institute of Mathematics》2013,280(1):240-247
Given a bounded set S of small measure, we discuss the existence of sampling sequences for the Paley-Wiener space PW S , which have both densities and sampling bounds close to the optimal ones. 相似文献
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Nadav Meir 《Mathematical Logic Quarterly》2015,61(4-5):341-346
A structure in a first‐order language is indivisible if for every colouring of its universe M in two colours, there is a monochromatic such that . Additionally, we say that is symmetrically indivisible if can be chosen to be symmetrically embedded in (that is, every automorphism of can be extended to an automorphism of ). In the following paper we give a general method for constructing new symmetrically indivisible structures out of existing ones. Using this method, we construct many non‐isomorphic symmetrically indivisible countable structures in given (elementary) classes and answer negatively the following question from 6 : Let be a symmetrically indivisible structure in a language . Let . Is symmetrically indivisible? 相似文献
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Yosef E. Maruvka Nadav M. Shnerb Sorin Solomon Gur Yaari David A. Kessler 《Journal of statistical physics》2011,142(6):1302-1316
The inference of past demographic parameters from current genetic polymorphism is a fundamental problem in population genetics.
The standard techniques utilize a reconstruction of the gene-genealogy, a cumbersome process that may be applied only to small
numbers of sequences. We present a method that compares the total number of haplotypes (distinct sequences) with the model
prediction. By chopping the DNA sequence into pieces we condense the immense information hidden in sequence space into a function
for the number of haplotypes versus subsequence size. The details of this curve are robust to statistical fluctuations and
are seen to reflect the process parameters. This procedure allows for a clear visualization of the quality of the fit and,
crucially, the numerical complexity grows only linearly with the number of sequences. Our procedure is tested against both
simulated data as well as empirical mtDNA data from China and provides excellent fits in both cases. 相似文献
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