全文获取类型
收费全文 | 21244篇 |
免费 | 1437篇 |
国内免费 | 1874篇 |
专业分类
化学 | 20244篇 |
晶体学 | 422篇 |
力学 | 680篇 |
综合类 | 87篇 |
数学 | 229篇 |
物理学 | 2893篇 |
出版年
2024年 | 5篇 |
2023年 | 198篇 |
2022年 | 330篇 |
2021年 | 352篇 |
2020年 | 625篇 |
2019年 | 661篇 |
2018年 | 702篇 |
2017年 | 964篇 |
2016年 | 1084篇 |
2015年 | 839篇 |
2014年 | 854篇 |
2013年 | 2176篇 |
2012年 | 1385篇 |
2011年 | 1180篇 |
2010年 | 1085篇 |
2009年 | 1305篇 |
2008年 | 1126篇 |
2007年 | 1194篇 |
2006年 | 1042篇 |
2005年 | 887篇 |
2004年 | 775篇 |
2003年 | 661篇 |
2002年 | 554篇 |
2001年 | 476篇 |
2000年 | 468篇 |
1999年 | 405篇 |
1998年 | 366篇 |
1997年 | 335篇 |
1996年 | 291篇 |
1995年 | 351篇 |
1994年 | 282篇 |
1993年 | 226篇 |
1992年 | 177篇 |
1991年 | 152篇 |
1990年 | 147篇 |
1989年 | 133篇 |
1988年 | 156篇 |
1987年 | 170篇 |
1986年 | 99篇 |
1985年 | 77篇 |
1984年 | 92篇 |
1983年 | 21篇 |
1982年 | 56篇 |
1981年 | 25篇 |
1980年 | 20篇 |
1979年 | 17篇 |
1978年 | 6篇 |
1977年 | 4篇 |
1973年 | 7篇 |
1957年 | 3篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
71.
A triangular lattice model for pattern formation by core-shell particles at fluid interfaces is introduced and studied for the particle to core diameter ratio equal to 3. Repulsion for overlapping shells and attraction at larger distances due to capillary forces are assumed. Ground states and thermodynamic properties are determined analytically and by Monte Carlo simulations for soft outer- and stiffer inner shells, with different decay rates of the interparticle repulsion. We find that thermodynamic properties are qualitatively the same for slow and for fast decay of the repulsive potential, but the ordered phases are stable for temperature ranges, depending strongly on the shape of the repulsive potential. More importantly, there are two types of patterns formed for fixed chemical potential—one for a slow and another one for a fast decay of the repulsion at small distances. In the first case, two different patterns—for example clusters or stripes—occur with the same probability for some range of the chemical potential. For a fixed concentration, an interface is formed between two ordered phases with the closest concentration, and the surface tension takes the same value for all stable interfaces. In the case of degeneracy, a stable interface cannot be formed for one out of four combinations of the coexisting phases, because of a larger surface tension. Our results show that by tuning the architecture of a thick polymeric shell, many different patterns can be obtained for a sufficiently low temperature. 相似文献
72.
Carla Ruggiero Stefania Ramirez Eric Ramazzotti Rita Mancini Roberto Muratori Maria Augusta Raggi Matteo Conti 《Journal of separation science》2020,43(8):1440-1449
In this work, a convenient method for the therapeutic monitoring of seven common antipsychotic drugs in “dried plasma spot” samples has been developed. It is based on the liquid chromatography tandem mass spectrometry technique, operating in multiple reaction monitoring mode, and a straightforward procedure for the simultaneous extraction of all antipsychotics in a single step, with high extraction yield. The method was fully validated with proper accuracy, precision, selectivity and sensitivity, for all the drugs. Limits of quantification were 0.12, 1.09, 1.46, 1.47, 5.70, 1.32, 1.33 µg/L for haloperidol, aripiprazole, olanzapine, quetiapine, clozapine, risperidone, and paliperidone, respectively. Accuracy, intra‐ and interday precision values were <10% for all drugs at all concentration levels examined. The method was tested in the analysis of 30 plasma samples from real patients for each drug. The proposed analytical approach, by combining practical and logistical advantages of microsampling with liquid chromatography tandem mass spectrometry analytical performance, could offer an ideal strategy for accurate and timely therapeutic drug monitoring of antipsychotic drugs in most clinical settings, even in remote centers and/or in out‐patient settings, bringing so many potential improvements in psychiatric patient care. 相似文献
73.
Shie-Chang Jeng 《Liquid crystals》2020,47(8):1223-1231
ABSTRACT The Tamm-plasmon-polariton (TPP) occurs at the interface between a metallic film and the photonic-crystal (PC) substrate. Unlike conventional surface-plasmon-polariton (SPP), TPP can be directly excited by both the transverse electric (TE) and transverse magnetic (TM) electromagnetic waves without using additional coupling optics. The fact that the optical functionality of most plasmonics devices is determined after fabrication limits their applications. Tunable SPP devices by applying liquid crystals (LCs) have been widely demonstrated due to their large birefringence and easy controllability via external stimuli. However, actively tuning TPP is difficult because the localised electric field is between the metallic film and PC substrate, the change of refractive index above the metallic film has only small influences on TPP. This article is intended to briefly review recent progress towards using LCs for actively tuning TPP devices. Not only TPP devices can gain benefits from LCs, we will also discuss the applications of TPP for measuring the anisotropy of the alignment films of LC devices. The sensitivity of the proposed scheme will be discussed. 相似文献
74.
In this study, a novel Cu-immobilized ionic liquid (IL)was designed, characterized, and employed as both promoter and solvent in the synthesis of some dihydropyrano[2,3-c]pyrazoles. The synthesized ionic liquid was characterized by 1H NMR, 13C NMR, FTIR, ICP and EDX analysis and showed high catalytic activity to proceed the synthesis of bioactive dihydropyrano[2,3-c]pyrazole derivatives. This method has the advantage of using the IL as a green medium for the synthesize of the products in high to excellent yields within short reaction times. 相似文献
75.
《Journal of Saudi Chemical Society》2020,24(3):321-333
Due to their structural merits that arise from their stability and high surface area, the layered double hydroxide (LDH) materials have caused strong attention. These characteristics provided intriguing possibilities with improved efficiency for catalytic applications. In this work, the preparation of 1-butyl-3-methylimidazolium hydroxide ([BMIM]+OH−) intercalated by a facile approach in a layered double hydroxide (LDH) matrix is reported and its implementation as a greener catalyst is shown. Different physico-chemical techniques such as XRD, FTIR, TGA, and N2-physisorption, HRTEM, and CO2 adsorption are implemented to characterize the structure of the fabricated catalysts. The [BMIM]+OH−/LDH exhibit outstanding catalytic performance in Knoevenagel condensation, resulting from the high LDH surface area and synergistic effects between both the intercalated ionic liquid and LDHs matrix. Knoevenagel’s fabricated catalysts can be exploited to catalyze different condensations and can be reused well. This work therefore generates good opportunities in the field of catalysis for the preparing and implementation of LDH-based catalysts. 相似文献
76.
Zhi Sun Mengfan Zhao Lihua Zuo Shengnan Zhou Feng Fan Qingquan Jia Lianping Xue Hanbing Li Jian Kang Xiaojian Zhang 《Journal of separation science》2022,45(2):518-528
Juglandis Mandshuricae Cortex is the bark of Juglans mandshurica Maxim., which has been used as a folk medicine plant in China and India. In this study, an ultra-high performance liquid chromatography–quadrupole/orbitrap high-resolution mass spectrometry method was developed to clarify and quantify the chemical profiling of Juglandis Mandshuricae Cortex rapidly. A total of 113 compounds were characterized. Among them, seven flavonoids were simultaneously quantified in 15 min, including myricetin, myricetrin, taxifolin, kaempferol, quercetin, quercitrin, and naringenin. The method was validated for accuracy, precision, and the limits of detection and quantification. All calibration curves showed a good linear relationship (r > 0.9990) within test ranges. The intra- and inter-day relative standard deviations were less than 2.16%. Accuracy validation showed that the recovery was between 95.6 and 101.3% with relative standard deviation values below 2.85%. The validated method was successfully applied to determine the contents of seven flavones in Juglandis Mandshuricae Cortex from seven sources and the contents of these places were calculated respectively. This method provides a theoretical basis for further developing the medicinal value of Juglandis Mandshuricae Cortex. 相似文献
77.
Michele Iannone Anna Pia Dima Francesca Sciarra Francesco Botrè Andrea M. Isidori 《Biomedical chromatography : BMC》2022,36(5):e5344
We present a liquid chromatography tandem mass spectrometry method for the simultaneous analysis of 16 endogenous steroids (androgens, estrogens, glucocorticoids and progestogens) in human serum. Samples (250 μl of matrix) were extracted with t-butylmethyl ether prior to LC–MS/MS analysis. The chromatographic separation was achieved on a reversed-phase column using a methanol–water gradient. The HPLC was coupled to a triple quadrupole mass spectrometer equipped with an electrospray ionization source with acquisition in multiple reaction monitoring mode. The method was validated using surrogate matrices and human serum samples. The specificity of the method was confirmed for all of the considered steroids; linearity was also assessed (R2 > 0.99, lack-of-fit test) in the ranges of concentrations investigated. The lower limits of quantification were in the range 10–400 pg/ml depending on the target steroid. Accuracy was in the range 85–115% for all target steroids except for the lower limit of quantitation levels where it was 80–120%. The extraction recovery was always >65%. No significant matrix effects were observed. To test the reliability of the method, the analysis of serum samples collected from 10 healthy subjects (5 M/5F) was performed. The present method can be used to identify the trajectories of deviation from the concentration normality ranges applied to disorders of the gonadal and adrenal axes. 相似文献
78.
Accurate quantification of polymer distributions is one of the main challenges in polymer analysis by liquid chromatography. The response of contemporary detectors is typically influenced by compositional features such as molecular weight, chain composition, end groups, and branching. This renders the accurate quantification of complex polymers of which there are no standards available, extremely challenging. Moreover, any (programmed) change in mobile‐phase composition may further limit the applicability of detection techniques. Current methods often rely on refractive index detection, which is not accurate when dealing with complex samples as the refractive‐index increment is often unknown. We review current and emerging detection methods in liquid chromatography with the aim of identifying detectors, which can be applied to the quantitative analysis of complex polymers. 相似文献
79.
Ho-Sang Shin 《Biomedical chromatography : BMC》2022,36(6):e5360
A method to determine 8 polychlorinated biphenyls (PCBs), 23 organochlorine pesticides (OCPs) and 16 polycyclic aromatic hydrocarbons (PAHs) was described using dispersive liquid–liquid microextraction (DLLME) of a small amount of plasma or serum sample and gas chromatography–tandem mass spectrometry (GC–MS/MS). The appropriate selection of the extraction solvent and dispersing solvent contributes to a high extraction yield and a clean extract. To verify the developed method, the interference, linearity of the calibration curve, detection limit, precision and accuracy were evaluated. The calibration curves were linear by 2–3 orders of magnitude with correlation coefficients above 0.997 in all cases. The LODs of PCBs, OCPs and PAHs were measured in the ranges of 0.0006–0.0029, 0.001–0.029 and 0.0002–0.012 ng/mL. The intraday precision achieved by this method was 2.19–10.3% (PCBs), 1.65–14.3% (OCPs) and 0.91–12.8% (PAHs), and the intraday accuracy 1.56–7.37% (PCBs), 2.34–19.6% (OCPs) and 1.49–15.7% (PAHs). The advantage of this method is that the analysis of PCBs, OCPs, and PAHs can be performed in a single chromatographic run, and the low detection limit enables monitoring of target substances in low exposure general public samples, and the analysis procedure is relatively simple and fast. 相似文献
80.
Thermoelectric(TE)energy harvesting can effectively convert waste heat into electricity,which is a crucial technology to solve energy concerns.As a promising candidate for energy conversion,poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate)(PEDOT:PSS)has gained significant attention owing to its easy doping,high transparency,and solution processability.However,the TE performance of PEDOT:PSS still needs to be further enhanced.Herein,different approaches have been applied for tuning the TE properties:(i)direct dipping PEDOT:PSS thin films in ionic liquid;(ii)post-treatment of the films with concentrated sulfuric acid(H2SO4),and then dipping in ionic liquid.Besides,the same bis(trifluoromethanesulfonyl)amide(TFSI)anion and different cation salts,including 1-ethyl-3-methylimidazolium(EMIM+)and lithium(Li+),are selected to study the influence of varying cation types on the TE properties of PEDOT:PSS.The Seebeck coefficient and electrical conductivity of the PEDOT:PSS film treated with H2SO4EMIM:TFSI increase simultaneously,and the resulting maximum power factor is 46.7μW·m-1·K-2,which may be attributed to the ionic liquid facilitating the rearrangement of the molecular chain of PEDOT.The work provides a reference for the development of organic films with high TE properties. 相似文献