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1.
Let G=(V(G),E(G)) be a graph. A (n,G, λ)‐GD is a partition of the edges of λKn into subgraphs (G‐blocks), each of which is isomorphic to G. The (n,G,λ)‐GD is named as graph design for G or G‐decomposition. The large set of (n,G,λ)‐GD is denoted by (n,G,λ)‐LGD. In this work, we obtain the existence spectrum of (n,P3,λ)‐LGD. © 2002 Wiley Periodicals, Inc. J Combin Designs 10: 151–159, 2002; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/jcd.10008 相似文献
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据不同地貌、地质条件在30个县市按剖面、同步、随机取土壤样品372份.测定硒等微量元素含量.作等级相关分析显示。土壤硒含量与消化系统癌呈负相关关系.作相对危险度、剂量-效应及多因素分析,认为此负相关关系并非偶然现象. 相似文献
4.
Yaqi Xu Qianwen Sun Wei Chen Yanqi Han Yue Gao Jun Ye Hongliang Wang Lili Gao Yuling Liu Yanfang Yang 《Molecules (Basel, Switzerland)》2022,27(21)
Taste masking of traditional Chinese medicines (TCMs) containing multiple bitter components remains an important challenge. In this study, berberine (BER) in alkaloids and phillyrin (PHI) in flavonoid glycosides, which are common bitter components in traditional Chinese medicines, were selected as model drugs. Chitosan (CS) was used to mask their unfriendly taste. Firstly, from the molecular level, we explained the taste-masking mechanism of CS on those two bitter components in detail. Based on those taste-masking mechanisms, the bitter taste of a mixture of BER and PHI was easily masked by CS in this work. The physicochemical characterization results showed the taste-masking compounds formed by CS with BER (named as BER/CS) and PHI (named as PHI/CS) were uneven in appearance. The drug binding efficiency of BER/CS and PHI/CS was 50.15 ± 2.63% and 67.10 ± 2.52%, respectively. The results of DSC, XRD, FTIR and molecular simulation further indicated that CS mainly masks the bitter taste by disturbing the binding site of bitter drugs and bitter receptors in the oral cavity via forming hydrogen bonds between its hydroxyl or amine groups and the nucleophilic groups of BER and PHI. The taste-masking evaluation results by the electronic tongue test confirmed the excellent taste-masking effects on alkaloids, flavonoid glycosides or a mixture of the two kinds of bitter components. The in vitro release as well as in vivo pharmacokinetic results suggested that the taste-masked compounds in this work could achieve rapid drug release in the gastric acid environment and did not influence the in vivo pharmacokinetic results of the drug. The taste-masking method in this work may have potential for the taste masking of traditional Chinese medicine compounds containing multiple bitter components. 相似文献
5.
Derong Shang Wenyan Gu Yuxiu Zhai Jinsong Ning Xuefei Mao Xiaofeng Sheng Yanfang Zhao Haiyan Ding Xuming Kang 《Molecules (Basel, Switzerland)》2022,27(24)
In this work, a rapid method for the simultaneous determination of N and S in seafood was established based on a solid sampling absorption-desorption system coupled with a thermal conductivity detector. This setup mainly includes a solid sampling system, a gas line unit for controlling high-purity oxygen and helium, a combustion and reduction furnace, a purification column system for moisture, halogen, SO2, and CO2, and a thermal conductivity detector. After two stages of purging with 20 s of He sweeping (250 mL/min), N2 residue in the sample-containing chamber can be reduced to <0.01% to improve the device’s analytical sensitivity and precision. Herein, 100 s of heating at 900 °C was chosen as the optimized decomposition condition. After the generated SO2, H2O, and CO2 were absorbed by the adsorption column in turn, the purification process executed the vaporization of the N-containing analyte, and then N2 was detected by the thermal conductivity cell for the quantification of N. Subsequently, the adsorbed SO2 was released after heating the SO2 adsorption column and then transported to the thermal conductivity cell for the detection and quantification of S. After the instrumental optimization, the linear range was 2.0–100 mg and the correlation coefficient (R) was more than 0.999. The limit of detection (LOD) for N was 0.66 μg and the R was less than 4.0%, while the recovery rate ranged from 95.33 to 102.8%. At the same time, the LOD for S was 2.29 μg and the R was less than 6.0%, while the recovery rate ranged from 92.26 to 105.5%. The method was validated using certified reference materials (CRMs) and the measured N and S concentrations agreed with the certified values. The method indicated good accuracy and precision for the simultaneous detection of N and S in seafood samples. The total time of analysis was less than 6 min without the sample preparation process, fulfilling the fast detection of N and S in seafood. The establishment of this method filled the blank space in the area of the simultaneous and rapid determination of N and S in aquatic product solids. Thus, it provided technical support effectively to the requirements of risk assessment and detection in cases where supervision inspection was time-dependent. 相似文献
6.
颜色视觉匹配中显示器颜色色差阈值的评价 总被引:9,自引:3,他引:6
为了对阴极射线管(Cathode ray tube,CRT)显示器颜色恰可辨别的小色差阈值进行评价,在中性灰背景下,用编制的颜色匹配程序,在CRT显示器上随机产生颜色,分别调节程序中R、G、B通道的值,使匹配色与随机色达到视觉上的一致,进行颜色视觉匹配实验,测量CRT显示器上随机色和匹配色的L*a*b*值.用不同的色差公式对实验数据分别从明度、色调、饱和度进行比较分析,色差公式评价小色差的性能是CIEDE2000优于CMC(2∶1)和CIEL*a*b*.在a*b*图上绘制实验颜色恰可辨别图.不同色差公式计算的CRT显示器恰可辨别小色差阈值不同. 相似文献
7.
牡蛎、缢蛏和菲律宾蛤仔中微量元素的分析研究 总被引:1,自引:1,他引:0
采用硝酸-高氯酸法消解样品,应用ICP—AES法测定了牡蛎、缢蛏和菲律宾蛤仔中Ca、Co、Cr、Cu、Fe、Mg、Mn、Ni、Se、Sr、V和Zn共12种微量元素。实验结果表明,3种贝类中均含有大量的Ca、Cu、Fe、Mn、Zn、Mg,还含有Co、Cr、Ni、Se、Sr和V等对人体有益的微量元素,是营养价值较高的海产品,可以作为人体补充微量元素的重要来源。 相似文献
8.
Lv Xinrong Wang Yanfang Wang Ying-ao Lin Xiaoyun Ni Yongnian 《Journal of Solid State Electrochemistry》2021,25(6):1871-1880
Journal of Solid State Electrochemistry - In this work, the binary nanocomposite of crosslinked polyaniline nanorods (CPANINRs) and molybdenum disulfide (MoS2) is first synthesized by in situ... 相似文献
9.
Yanfang Liu Naiming Qi Zhiwei Tang 《Journal of Optimization Theory and Applications》2013,156(2):345-364
A new guidance law is proposed for interceptor missiles by using a differential game formulation with bounded controls. The interceptor is steered by the aerodynamic-lift control system and the divert-thrusters control system. By using game space decomposition, the parameter effects of divert-thrusters control system on homing performance are investigated. Under propellant limits and given the time constant of the divert-thrusters control system, the hit-to-kill performance requires the following conditions. Firstly, the maximum acceleration generated by the divert-thrusters control system is greater than a critical value. Secondly, the thrusters close after interception terminates. Thirdly, the operation time of the divert-thrusters control system is sufficient long to cancel the miss distance. These results are also demonstrated by a realistic ballistic missile-defense simulation program. 相似文献
10.
Yanfang Liu Yuansheng Xiao Xingya Xue Xiuli Zhang Xinmiao Liang 《Rapid communications in mass spectrometry : RCM》2010,24(5):667-678
During the discovery process of novel compounds, it is of significant importance to differentiate novel from known compounds in crude extracts before starting the time‐consuming process of purification. Bufadienolides are the main active components of the skin of the toad Bufo bufo gargarizans Cantor (toad skin), an important traditional Chinese medicine. The fragmentation behavior and mass spectra profiles of bufadienolides standards were investigated using ultra‐performance liquid chromatography/electrospray ionization quadrupole time‐of‐flight mass spectrometry (UPLC/ESI‐Q‐TOFMS). Several fragmentation rules were summarized and applied to characterize novel and known bufadienolides in toad skin. Characteristic substituent groups could be identified by both diagnostic ions and their relative abundance. Bufadienolide stereoisomers could be differentiated from positional isomers by comparing fragment abundance profiles. This was used to characterize new stereoisomers for known bufadienolides. A total of 39 bufadienolides were screened out using a systematic method developed in our laboratory. In addition to 19 known bufadienolides, 20 putative novel compounds, including 8 stereoisomers, were characterized. UPLC/Q‐TOFMS was demonstrated to be a powerful tool for the characterization of low‐abundance bufadienolides in complex samples. This study provides guidelines for the targeted isolation of novel bufadienolides from natural products. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献