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61.
Abstract Analogous to most new methods in science, photoacoustic spectroscopy (PAS) grew out of an advance in technology, in this case the dramatic improvement in novel light sources, modulators, and acoustic detectors, as well as signal recovery electronics, which in turn was made possible by the development of modern PAS techniques. PAS is a promising technique that can be used to analyze and characterize a broad variety of objects (gaseous, solid, and liquid samples). In the present review, the recent development of infrared PAS limited to the general area of gas-phase analysis techniques since 1990 is summarized, with special emphasis on the development of new or enhanced analytical methodologies based on the use of the photoacoustic (PA) effect to improve the sensitivity of PAS by enhancing signal or reducing noise levels, with regard to PA systems, applications, and conclusions. The applications of these novel PA methods are mainly concerned with molecular spectroscopic, industrial, atmospheric, environmental, chemical and biological, and medical and clinical analysis. New prospects and challenges in various application fields of PAS technique are described. 相似文献
62.
Dr. Xinhao Shi Wei Gu Dr. Cuiling Zhang Longyun Zhao Prof. Li Li Weidong Peng Prof. Yuezhong Xian 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(16):5643-5648
The development of highly sensitive and selective methods for the detection of lead ion (Pb2+) is of great scientific importance. In this work, we develop a new surface‐enhanced Raman scattering (SERS)‐based sensor for the selective trace measurement of Pb2+. The SERS‐based sensor is assembled from gold nanoparticles (AuNPs) and graphene using cucurbit[7]uril (CB[7]) as a precise molecular glue and a local SERS reporter. Upon the addition of Pb2+, CB[7] forms stronger complexes with Pb2+ and desorbs from AuNPs, resulting in a sensitive “turn‐off” of SERS signals. This SERS‐based assay shows a limit of detection (LOD) of 0.3 nm and a linear detection range from 1 nm to 0.3 μm for Pb2+. The feasibility of the assay is further demonstrated by probing Pb2+ in real water samples. This SERS‐based analytical method is highly sensitive and selective, and therefore holds promising applications in environmental analysis. 相似文献
63.
With the advantages of transmitting energy from multiple directions to one direction and transforming vibration from one source to multiple directions, the two-dimensional vibra?tion direction converter has important applications in power ultrasonic technology. However, for the complexity of using the wave equation to design and analysis the two-dimensional vibration direction converter, a concise equivalent circuit for the converter is investigated. By introducing the two-dimensional mechanical coupling coefficient and the longitudinal force transform coef?ficient, and using the electromechanical analogy principle, the equivalent circuit and resonance frequency equation of the two-dimensional vibration direction converter vibrating in anti-phase and in-phase two-dimensional coupled vibration are deduced. The resonance frequencies of the vibration direction converters of two different materials are calculated by using the proposed frequency equation, which are in agreement with the results from the finite element method and the experimental test. It provides a concise method for the design and applications of such ultrasonic vibration system. 相似文献
64.
Lianwei Li Xu Wang Chen He Weidong He 《Journal of polymer science. Part A, Polymer chemistry》2014,52(1):128-138
Amphiphilic hyperbranched copolymer chains made of large hyperbranched poly(acrylic acid) cores grafted with short polystyrene stickers (HB‐PAAn‐g‐PSn + 1) with different n values (n = 1, 10, 47) were well prepared and confirmed by size exclusion chromatography, Fourier transform infrared spectroscopy and 1H nuclear magnetic resonance. The study on the interchain association behavior of these amphiphilic chains indicates that larger HB‐(PAA)n‐g‐(PS)n + 1 copolymer chains have a less tendency to undergo interchain association. Moreover, the simple vial‐inversion and rheological experiments show that the apparent critical gel concentration (Cg) decreases with n, but no sol–gel transition was observed for triblock PS‐PAA‐PS even when the concentration is up to 200 g L?1. Further transmission electron microscopy study of the latex particles prepared with HB‐(PAA)n‐g‐(PS)n + 1 as surfactant reveals that the latex particles are spherical and narrowly dispersed; while the measured latex particle number (Np) indicates the surfactant efficiency of HB‐(PAA)47‐g‐(PS)48 is poorer than that of triblock PS‐PAA‐PS (n = 1). Finally, pyrene solubilization measurement shows the solubilization efficiency of HB‐(PAA)n‐g‐(PS)n + 1 copolymers decreases with n, consistent with the previous observed interchain association result. The present study demonstrates that both the chain topology and the styrene weight fraction dominates the final solution properties of amphiphilic HB‐(PAA)n‐g‐(PS)n + 1 chains in aqueous solution. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 128–138 相似文献
65.
Yongtao Bai Lihua Song Yongheng Zhang Guoliang Dai Weidong Zhang Shanshan Song Hong Sun Wen Jing Meijuan Xu Wenzheng Ju 《Biomedical chromatography : BMC》2019,33(9)
A highly selective and efficient LC–MS/MS method was developed to determine the plasma concentration of magnolol, hesperidin, neohesperidin and geniposide following oral administration of Zhi‐Zi‐Hou‐Po decoction in normal and depressed rats. Plasma samples were pretreated by protein precipitation with methanol. Chromatographic separation was performed on an XTerra® MS C18 column using a gradient elution with a mobile phase composed of acetonitrile–0.1% aqueous formic acid. The proposed method was validated to be specific, accurate and precise for the analytes determination in plasma samples. The calibration curves displayed good linearity over definite concentration ranges for the analytes. The intra‐ and inter‐day precision of the proposed method at three different levels were all within <11.13% and the relative errors ranged from ?8.46 to 8.93%. The recovery of the four compounds ranged from 82.72 to 89.08% and no apparent matrix effect was observed during sample analysis. After full validation, the established method was successfully applied for comparing the pharmacokinetics of four components between normal and depressed rats. The results showed that the AUC and Cmax of four analytes in depressed rats were significantly different from those in normal rats and might provide helpful information to guide the clinical use of Zhi‐Zi‐Hou‐Po to treat depression. 相似文献
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68.
目的 通过分析高龄老年(≥80岁)男性腰椎骨密度(LBMD)的独立相关因素,寻找提高高龄老年男性LBMD 的方法。方法 对1066例高龄老年男性进行LBMD测定、血液生化、骨代谢和生殖激素等指标的检测,运用多元回归分析筛选高龄老年男性LBMD 的独立相关因素。结果 高龄老年男性LBMD的独立相关因素有体重指数(β=0.018,P<0.01)、I型胶原羧基端肽β特殊序列(β=-0.226,P<0.01)、慢性阻塞性肺疾病(β=-0.047,P<0.01)、雌二醇(β=0.002,P<0.01)。结论 维持合理的体重指数和雌二醇水平,降低血清I型胶原羧基端肽β特殊序列水平,积极防治慢性阻塞性肺疾病,可能是提高高龄老年男性LBMD的重要方法。 相似文献
69.
Pengfei Sun Biao Deng Guohao Du He Li Weidong Sun Jiangbo Ren Tiqiao Xiao 《X射线光谱测定》2015,44(6):442-446
X‐ray fluorescence computed tomography is an emerging imaging modality that allows for the nondestructive reconstruction of the internal distribution of elements within a sample. The common use of X‐ray excitation energy (up to approximately 20 keV) has necessitated the use of l ‐shell fluorescence for heavy elements. In this study, based on high energy X‐ray at BL13W1 of the Shanghai Synchrotron Radiation Facility, we employed high‐energy excitation for tomographic imaging of the heavy metals (rare earth elements) in fish teeth from deep‐sea sediments on the micrometer scale using K‐shell X‐ray fluorescence. The virtual cross‐sectional distribution of La, Ce, Pm, Pr, Nd, and Sm were obtained, thereby providing a feasible approach for analyzing the enrichment mechanism of rare earth elements. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
70.
Lisa M. Jones Hao Zhang Weidong Cui Sandeep Kumar Justin B. Sperry James A. Carroll Michael L. Gross 《Journal of the American Society for Mass Spectrometry》2013,24(6):835-845
As therapeutic monoclonal antibodies (mAbs) become a major focus in biotechnology and a source of the next-generation drugs, new analytical methods or combination methods are needed for monitoring changes in higher order structure and effects of post-translational modifications. The complexity of these molecules and their vulnerability to structural change provide a serious challenge. We describe here the use of complementary mass spectrometry methods that not only characterize mutant mAbs but also may provide a general framework for characterizing higher order structure of other protein therapeutics and biosimilars. To frame the challenge, we selected members of the IgG2 subclass that have distinct disulfide isomeric structures as a model to evaluate an overall approach that uses ion mobility, top-down MS sequencing, and protein footprinting in the form of fast photochemical oxidation of proteins (FPOP). These three methods are rapid, sensitive, respond to subtle changes in conformation of Cys?→?Ser mutants of an IgG2, each representing a single disulfide isoform, and may be used in series to probe higher order structure. The outcome suggests that this approach of using various methods in combination can assist the development and quality control of protein therapeutics. 相似文献