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111.
Kyung Mi Lee Xiaoqiang Chen Wang Fang Jong‐Man Kim Juyoung Yoon 《Macromolecular rapid communications》2011,32(6):497-500
A PDA based sensor, derived from a di‐(2‐picolyl) amine (DPA) substituted diacetylene monomer, displayed a selective colorimetric change and a large fluorescence enhancement in the presence of lead ions. The lead selective PDA‐based chemosensor enabled easy detection of the presence of lead in 100% aqueous solution by the naked‐eye.
112.
113.
M. Piñeiro-Iglesias M. Miñones-Vázquez E. Vázquez-Blanco S. Muniategui-Lorenzo P. López-Mahía D. Prada-Rodríguez 《Chromatographia》2002,56(7-8):483-488
Summary The aim of this work is to establish the best conditions for concentration and purification steps in the trace analysis of
aliphatic and polycyclic aromatic hydrocarbons (PAH) from atmospheric particulate matter by gas chromatography-flame ionisation
detection (GC-FID) and high performance liquid chromatography with ultraviolet and fluorescence detection (HPLC-UV-FL). The
best results for the more volatile compound were obtained with a combination of rotary evaporation and a stream of nitrogen
(near to 100% for aliphatic hydrocarbons and from 70 to 105% for PAH). Two types of solid phase extraction (SPE)cartridges
(Supelclean
tm
LC-Silica SPE tubes and Sep-Pak? Plus silica cartridges) and glass column were examined for the purification and fractionation step. Blank chromatograms of
both types of cartridges analysed by GC-FID made this study difficult, because a PSS (programmed split-splitless) injector
was employed thereby increasing the sensitivity. This problem was not observed in the HPLC-UV-FL blank chromatograms of these
cartridges. Glass columns filled with silica and alumina were chosen because no interference was found in the GC-FID blank
chromatograms and the best recoveries in the fractionation of both aliphatic hydrocarbons and PAH were achieved. This is especially
important when aliphatic hydrocarbons concentrations are lower than 1 μg mL−1. Finally, the selected conditions were applied to the analysis of hydrocarbons in real atmospheric particulate samples. 相似文献
114.
用ICP-AES法测定了东太平洋深海锰结核样品中二十多种主,次及微量元素,结果表明,表面瘤状和表面光滑两种类型锰结核的化学元素含量有较明显的区别,如表面光滑的锰结核TiO2含较高,而表面瘤状的锰结核Mn/Fe之值较高等。 相似文献
115.
There is a need for a better characterization of sludges from wastewater treatment plants which are destined to be spread on agricultural lands. Inorganic pollutants are regularly controlled but organic pollutants have received few attention up to now. On this paper, we have been interested on the analysis of the 16 polycyclic aromatic hydrocarbons (PAHs) listed in the US Environmental Protection Agency (US EPA) priority list and more particularly of the six PAHs listed in the European community list (fluoranthene, benzo[b and k]fluoranthene, benzo[a]pyrene, benzo[ghi]perylene, indeno[1,2,3-cd]pyrene). The analysis step consists on liquid chromatography with both fluorescence and UV detections as described in the EPA Method 8310. As for the extraction step, several techniques such as supercritical fluid extraction, pressurized liquid extraction, focused microwave extraction in open vessels, Soxhlet and ultrasonic extractions are compared after optimization of the experimental conditions (solvent nature and quantity, temperature, pressure, duration, ... ) and validation with certified sludges. When optimized, these five extraction techniques are as much efficient with similar relative standard deviation. Whatever the extraction techniques used, the whole analysis protocol permits to quantify PAHs in the range of 0.09 to 0.9 mg/kg of dried sludges. 相似文献
116.
合成了一种棒形的化合物4,4'-二(α-腈基-4-苯丙氧基苯乙烯)联苯(Ben-DCSB), 利用核磁共振(NMR)、质谱(EI-MS)、傅里叶变换红外光谱(FT-IR)和元素分析等对其进行了结构表征. 对Ben-DCSB重结晶粉末进行研磨后, 其发光颜色从蓝绿色变成黄绿色, 荧光量子效率(ΦF)从初始的52.7%变为38.7%, 表明该化合物具有力致变色性质. 扫描电子显微镜(SEM)、X-射线衍射(XRD)和荧光寿命等测试结果显示, 这种现象是由于在外界环境刺激下改变了Ben-DCSB在聚集态下的分子堆积结构所造成的. 研磨后的样品暴露在溶剂蒸气(乙醇、二氯甲烷、四氢呋喃或丙酮)或100 ℃温度下放置2 min又能转换回初始状态的蓝绿色荧光, 表明化合物研磨后的样品具有气致和热致变色性能, 且展现出可逆变色性能. 对该化合物进行多次“力-溶剂蒸气刺激”和“力-热刺激”循环实验, 结果显示其具有很好的荧光可逆转换性能. 热分析结果显示化合物Ben-DCSB在194 ℃和212 ℃间存在向列相(纹影织构)的液晶态; 其热分解温度为362 ℃, 表明该化合物具有较好的热稳定性. 相似文献
117.
Xiantong Guan Bing Ding Xiaofeng Liu Jiajia Zhu Changhuan Mi Xiaogang Zhang 《Journal of Solid State Electrochemistry》2013,17(7):2087-2093
Li-rich layered Li1.2Ni0.2Mn0.6O2 has been surface modified by nickel–manganese composite oxide (Ni0.5Mn1.5O x ) to serve as a novel cathode material with novel layered spinel structure for lithium-ion battery. The as-prepared Li1.2Ni0.2Mn0.6O2 before and after surface modification by Ni0.5Mn1.5O x as well as simply blended Li1.2Ni0.2Mn0.6O2 with spinel LiNi0.5Mn1.5O4, have been characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electronic microscopy, and differential scanning calorimetry. Electrochemical studies indicate that the Ni0.5Mn1.5O x surface modified Li1.2Ni0.2Mn0.6O2 with peculiar layered spinel character dramatically represented increased discharge capacity, improved cycling stability as well as excellent rate capability at high-voltage even up to 5.0 V. 相似文献
118.
Liu Q Hong IP Ahn MJ Yoo HS Han SB Hwang BY Lee MK 《Natural product communications》2011,6(12):1839-1841
Inhibition of adipocytes differentiation is suggested to be an important strategy for prevention and/or treatment of obesity. In our present study, Cordyceps militaris showed significant inhibitory activity on adipocyte differentiation in 3T3-L1 preadipocytes as assessed by measuring fat accumulation using Oil Red O staining. Activity-guided fractionation led to the isolation of cordycepin (1), guanosine (2) and tryptophan (3) as active compounds. All the three compounds were more effective in the prevention of early stage of adipogenesis than in lipolysis. In addition, combinational treatment of three compounds significantly increased anti-adipogenic activity. 相似文献
119.
为提高小檗碱的水溶性以及降糖活性,对其C-9位进行了结构修饰,合成了6个9-O-小檗碱酯类衍生物(3a~3f),其中3b~3d和3f为新化合物,其结构经1H NMR, IR和HR-MS(ESI)表征。选用人肝癌细胞(HepG2)建立胰岛素抵抗模型(HepG2-IR),通过MTT法研究了3a~3f的体外降糖活性。结果表明:3a~3f均具有不同程度的降糖活性,其中化合物3a(IC50=0.044 ±0.97 mg·L-1)在低浓度0.08 mg·L-1时,对HepG2-IR细胞葡萄糖消耗量为3.5 mM,优于小檗碱(2.75 mM)。 相似文献
120.
Ju-Kyung Shin So Mi Jeong Yongsug Tak Sung-Hyeon Baeck 《Research on Chemical Intermediates》2010,36(6-7):715-724
MoO3/Pt binary catalysts with various Mo/Pt ratios were prepared by an electrodeposition method for use as the anode in a direct methanol fuel cell. Pt was electrodeposited onto indium tin oxide (ITO) substrate, and then MoO3 was electrodeposited from an Mo-peroxo electrolyte on the top of Pt with different deposition times. The crystallinity of synthesized films was analyzed by X-ray diffraction (XRD), and the oxidation state of both the platinum and molybdenum were determined by X-ray photoelectron spectroscopy (XPS) analyses. Scanning electron microscopy–energy dispersive X-ray spectroscopy (SEM/EDS) was employed to investigate the surface morphology and composition. The catalytic activity and stability for methanol oxidation were measured using cyclic voltammetry and chronoamperometry in a mixture of 0.5 M H2SO4 and 0.5 M CH3OH aqueous solution. Electrocatalytic activity for CO oxidation was also evaluated in a 0.5-M H2SO4 solution. The addition of a proper amount of MoO3 was found to significantly improve both the catalytic activity and stability for methanol oxidation. 相似文献