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排序方式: 共有259条查询结果,搜索用时 15 毫秒
51.
Hydrodynamic cavitation has been investigated extensively in the field of water treatment in the last decade and a well-designed hydrodynamic cavitation reactor is critical to the efficient removal of algal and large-scale application. In this paper, a jet pump cavitation reactor (JPCR) is developed for the removal of cyanobacteria Microcystis aeruginos in a pilot scale. The results demonstrate that the photosynthetic activity of M. aeruginosa is greatly inhibited immediately after treatment in the JPCR, and the growth is also hindered after 3 days culture. Moreover, a high cell disruptions of M. aeruginosa is detected after treated by JPCR. The release of chlorophyll-a indicates that the JPCR caused serious rupture to M. aeruginosa cells. The plausible cell disruption mechanisms are proposed in accordance with a fluorescence microscope and scanning electron microscope. Then, the optimization of cell disruption efficiency is also investigated for various operating conditions. The results showed that the algal cell disruption efficiency is improved at higher inlet pressure and the cavitation stage between the unstable limited operation cavitation stage and stable limited operation cavitation stage. The effect and optimization of JPCR on algal reduction are highlighted. The results of the study promote the application of hydrodynamic cavitation on algal removal and provide strong support for JPCR application in algal removal. 相似文献
52.
Jermiah Y. Shen Matt S. Chang Sheng‐Hsiung Yang Gaston J. Wu 《Journal of separation science》2012,35(19):2544-2552
The presence of triclosan and triclocarban, two endocrine‐disrupting chemicals and antimicrobial agents, and transformation products of triclocarban, 1,3‐di(phenyl)urea, 1,3‐bis(4‐chlorophenyl)urea and 1,3‐bis(3,4‐dichlorophenyl)urea, in tap water, treated household drinking water, bottled water, and river water samples were investigated using solid‐phase micro‐extraction coupled with‐HPLC‐MS/MS, a rapid, green, and sensitive method. Factors influencing the quantity of the analytes extracted onto the solid‐phase micro‐extraction fiber, such as addition of salt, sample pH, extraction time, desorption time, and sample volume, were optimized using solid‐phase micro‐extraction‐HPLC‐MS/MS. The results showed that the method gave satisfactory sensitivities and precisions for analyzing sub‐part‐per‐trillion levels of triclosan, triclocarban, and transformation products of triclocarban in samples collected locally. The recoveries of analytes ranged from 97 to 107% for deionized water samples, and 99 to 110% for river water samples, and limits of detection were in the range of 0.32–3.44 and 0.38–4.67 ng/L for deionized water and river water samples, respectively. On average, the daily consumption of triclosan and triclocarban by an adult by consuming 2 liters of different types of drinking water were estimated to be in the range of 6.13–425 ng/day as a result of the concentrations of triclosan and triclocarban measured in this study. 相似文献
53.
L. Connolly 《Trends in analytical chemistry : TRAC》2011,30(2):227-238
Endocrine-disrupting chemicals (EDCs) are capable of interfering with normal hormone homeostasis by acting on several targets and through a wide variety of mechanisms. Unwanted exposure to EDCs can lead to a wide spectrum of adverse health effects, especially when exposure is during critical windows of development. Feed and food are considered to be among the main routes of inadvertent exposure to EDCs, so there is an important need for efficient detection of EDCs in these matrices.We describe in vitro bioassays that can complement current analytical chemistry in order to detect unwanted EDCs and describe their action, emphasizing assays that can measure effects on nuclear receptor signaling or hormone production. We outline both validated and unvalidated in vitro assays currently available in the scientific community for detecting and studying the effects of EDCs, and discuss their possible role in the food-safety context. We conclude by identifying gaps in the current battery of in vitro assays available for EDCs and suggest future possibilities for development and validation. 相似文献
54.
在单机重新排序问题中,一个原始工件集已经排好顺序,使得给定的目标函数最小.当一个新的工件集到来时就会产生一些错位,决策者需要插入新工件到原来排序中而还不能过分打乱它们的顺序.该论文首先研究了当工件加工时间和工期相容时,在错位量限制的条件下最小化最大延迟问题;也研究了当工件加工时间相同或工件工期相同时,在错位量限制的条件下最小化误工和问题.对这些问题,给出了好的算法. 相似文献
55.
利用傅里叶分析和相关分析方法,研究了HL-1装置等离子体MHD不稳定性的特征和抑制不稳定性的若干方法及结果,给出了HL-1装置的稳定运行区域。 相似文献
56.
对于机器排序的应急管理问题,Qi Xiang-tong等人进行了系统分析,得出了较好的结果.此文则考虑带可分配工期的总误工问题的应急管理问题.对于不同模型,或给出其最优序,或给出其近似解. 相似文献
57.
58.
Among the various compounds considered as emerging pollutants, alkylphenolic surfactants, steroid sex hormones, and pharmaceuticals are of particular concern, both because of the volume of these substances used and because of their activity as endocrine disruptors or as causative agents of bacterial resistance, as is the case of antibiotics. Today, the technique of choice for analysis of these groups of substances is liquid-chromatography coupled to mass spectrometry (LC–MS) and tandem mass spectrometry (LC–MS–MS). In the last decades, this technique has experienced an impressive progress that has made possible the analysis of many environmental pollutants in a faster, more convenient, and more sensitive way, and, in some cases, the analysis of compounds that could not be determined before. This article reviews the LC–MS and LC–MS–MS methods published so far for the determination of alkylphenolic surfactants, steroid sex hormones and drugs in the aquatic environment. Practical considerations with regards to the analysis of these groups of substances by using different mass spectrometers (single quadrupole, ion trap and triple quadrupole instruments, etc.), interfaces and ionization and monitoring modes, are presented. Sample preparation aspects, with special focus on the application of advanced techniques, such as immunosorbents, restricted access materials and molecular imprinted materials, for extraction/purification of aquatic environmental samples and extracts are also discussed. 相似文献
59.
Recombinant human estrogen, androgen and progesterone receptors for detection of potential endocrine disruptors 总被引:9,自引:0,他引:9
Scippo ML Argiris C Van De Weerdt C Muller M Willemsen P Martial J Maghuin-Rogister G 《Analytical and bioanalytical chemistry》2004,378(3):664-669
This work reports the binding capacity of various chemicals (so-called endocrine disruptors) to recombinant human steroid receptors (hER, hPR and hAR). The tested chemicals are organochlorine insecticides (DDT and its metabolites, methoxychlor, aldrin, dieldrin, chlordecone, lindane, trichlorobenzene), estrogenic insecticides (endosulfan, toxaphene, nonachlor), herbicides (alachlor and atrazine), fungicides (benomyl and vinclozolin), industrial chemicals (nonylphenol, bisphenol A, diphenylphtalate), antioxidants (butylated hydroxyanisol) and some phytoestrogens. Except for phytoestrogens, most of the tested chemicals (DDT and its metabolites, aldrin, - and -endosulfan, toxaphen, trans-nonachlor) show higher affinities for hPR than for hER, indicating that the interaction with the progesterone receptor could contribute to the endocrine-disrupting effects imputed to these chemicals. We propose to use binding assays using recombinant human steroid receptors as screening tools for the detection of endocrine disruptors in various samples. 相似文献
60.
Seifert M 《Analytical and bioanalytical chemistry》2004,378(3):684-687
The analytics of endocrine-disrupting compounds has become a major issue during recent years. Several test systems have been developed for endocrine-disrupting chemicals. Yeast reporter gene assays and MCF-7 cell-based proliferation assays (E-screen) are particularly popular. A correlation of an enzyme-linked receptor assay (ELRA) with a yeast reporter gene assay is shown. In addition, the development of an ultra-sensitive luminescent ELRA with a detection limit of 20 ng/L for 17-estradiol in the sample is reported. Data for real sample analysis are shown in this paper. ELRA characteristics are compared with cell-based assays, and the issue of detection limits is addressed. In this context, the detection limits of the cell-based assays have been claimed to be below the ELRA detection limits. However, it is clarified that the given detection limits for the yeast estrogen screen and the E-screen are usually based on concentrations of 17-estradiol in the well, not in the sample, whereas ELRA detection limits are concentrations in the sample. 相似文献