全文获取类型
收费全文 | 2939篇 |
免费 | 160篇 |
国内免费 | 412篇 |
专业分类
化学 | 2547篇 |
晶体学 | 15篇 |
力学 | 10篇 |
综合类 | 15篇 |
数学 | 3篇 |
物理学 | 262篇 |
综合类 | 659篇 |
出版年
2024年 | 6篇 |
2023年 | 22篇 |
2022年 | 91篇 |
2021年 | 98篇 |
2020年 | 97篇 |
2019年 | 77篇 |
2018年 | 73篇 |
2017年 | 109篇 |
2016年 | 144篇 |
2015年 | 109篇 |
2014年 | 151篇 |
2013年 | 233篇 |
2012年 | 177篇 |
2011年 | 169篇 |
2010年 | 144篇 |
2009年 | 171篇 |
2008年 | 179篇 |
2007年 | 181篇 |
2006年 | 166篇 |
2005年 | 162篇 |
2004年 | 124篇 |
2003年 | 92篇 |
2002年 | 81篇 |
2001年 | 80篇 |
2000年 | 74篇 |
1999年 | 66篇 |
1998年 | 77篇 |
1997年 | 62篇 |
1996年 | 69篇 |
1995年 | 54篇 |
1994年 | 42篇 |
1993年 | 22篇 |
1992年 | 22篇 |
1991年 | 21篇 |
1990年 | 7篇 |
1989年 | 10篇 |
1988年 | 13篇 |
1987年 | 10篇 |
1986年 | 6篇 |
1985年 | 5篇 |
1984年 | 2篇 |
1983年 | 3篇 |
1982年 | 4篇 |
1981年 | 3篇 |
1979年 | 2篇 |
1978年 | 1篇 |
排序方式: 共有3511条查询结果,搜索用时 15 毫秒
61.
The aim of this paper is the preparation and characterization of cellulose/chitin blend filaments over the experimental blend ratio scope i.e., 2.89 and 6.46% (w/w) chitin content through high wet modulus (HWM) procedure. The spinnability of the invested solutions was found to vary in the following order: chitin < cellulose < 9.5:0.5 blend < 9:1 blend < 8:2 blend < 5:5 blend (9:1 means the mass ratio of cellulose to chitin, so does 9.5:0.5, 8:2, and 5:5). The cross‐section of the blend filaments is of chrysanthemum shape. It was shown through the SEM photographs that there existed grooves on the surface of filaments, which became coarse with increase in chitin content. Based on the data from X‐ray, sonic velocity, intensity, and hygroscopicity, it is concluded that the degree of crystallinity, dry and wet intensity modulus, degree of orientation, and regain rate of the filaments decreased with increase in chitin content in the experiment scope. The mechanical properties of the blend filaments are much higher than those of Crabyon fiber and normal viscose filaments, which proves that the HWM method is an efficient way of preparing cellulose/chitin blend filaments with satisfactory mechanical properties and processing property. The blend filaments prepared have an effective biostatic effect on Staphylococcus aureus, Escherchia coli, and Corinebaterium michiganence according to different testing standards. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
62.
63.
Elnaz Marzi Khosrowshahi Behnaz Limuie Khosrowshahi Mir Ali Farajzadeh Abolghasem Jouyban Mustafa Tuzen Mohammad Reza Afshar Mogaddam Mahboob Nemati 《Biomedical chromatography : BMC》2022,36(7):e5371
A dispersive solid-phase extraction method based on a new sorbent has been performed on plasma and wastewater samples to determine metoprolol by high-performance liquid chromatography–tandem mass spectrometry. In this study, the analyte was adsorbed from the samples onto microcrystalline cellulose as a green and efficient sorbent and then eluted for use in the determination step. In the mass spectrometer, the analyte was detected in the positive mode and selectivity of the analysis was increased by sequential mass analysis through multiple reaction monitoring. All of the effective parameters in the extraction of metoprolol from plasma and wastewater were optimized. Under optimal conditions the method was linear in the ranges of 1–1,000 and 0.1–1,000 ng/ml in plasma and wastewater samples, respectively. The detection limits of the method were 0.30 and 0.03 ng/ml in plasma and wastewater samples, respectively. The data showed that the method provides low detection limit, wide linear range, good precision and high extraction recovery. Finally several plasma and wastewater samples were successfully analyzed using the method. The use of a small amount of a green and inexpensive sorbent and a low volume of plasma without the need for further pretreatment steps are the main advantages of the method. 相似文献
64.
《Journal of Saudi Chemical Society》2022,26(6):101541
This research aims to fabricate and characterize chemically crosslinked CMC/PVP-co-poly (AMPS) based hydrogel for the sustained release of model drug metoprolol tartrate through the free radical polymerization technique. Box-Behnken Design was used to optimize CMC/PVP-co-poly (AMPS) hydrogel by varying the content of reactants such as; polymers (CMC and PVP), monomer (AMPS), and crosslinker (EGDMA). Carboxymethyl cellulose (CMC) was crosslinked chemically with AMPS with a constant ratio of PVP by the ethylene glycol dimethacrylate as the crosslinker in the presence of sodium hydrogen sulfite (SHS)/ammonium peroxodisulfate (APS) as initiators. After developing CMC-based hydrogels using different polymers, monomer, and crosslinker concentrations, this study encompassed dynamic swelling, sol–gel fraction, drug release and chemical characterizations such as FTIR, XRD, TGA, DSC, and SEM. In vitro drug release and swelling were performed at 1.2 and 6.8 pH to determine the sustained release pattern and pH-responsive behavior. These parameters depended on the crosslinker, polymer, and monomer ratios used in the formulation development. XRD, SEM, and FTIR showed the successful grafting of constituents resulting in the formation of a stable hydrogel. DSC and TGA confirmed the thermodynamic stability of the hydrogel. Hydrogel swelling was increased with an increase in the ratio of monomer; however, an increase in the ratio of polymer and crosslinker decreased the hydrogel swelling. In vitro gel fraction and drug release also depended on polymer, monomer, and crosslinker ratios. The fabricated CMC/PVP-co-poly (AMPS) hydrogels constituted a potential system for sustained drug delivery. 相似文献
65.
《Arabian Journal of Chemistry》2022,15(7):103933
In this study, a fingerprint-activity relationship modeling between chemical fingerprints and antirheumatic activity was established, and multivariate statistical analysis was used to evaluate the quality of Taxilli Herba (TH) from different hosts. Characteristic fingerprints of 20 batches of TH samples were generated by high-performance liquid chromatography coupled with triple quadrupole-time of flight tandem mass spectrometry (HPLC-Triple TOF-MS/MS), and the similarity analysis was calculated based on thirteen common characteristic peaks by hierarchical clustering analysis (HCA). Subsequently, nine efficacy markers were discovered by combining fingerprints and antirheumatic activity through grey correlation analysis (GCA) and bivariate correlation analysis (BCA). Meanwhile, the content of 5 constituents in 9 markers was determined by high-performance liquid chromatography coupled with triple quadrupole-linear ion trap tandem mass spectrometry (HPLC-QTRAP-MS/MS). The comprehensive quality of TH was assessed using multivariate statistical analysis, including principal components analysis (PCA) and technique for order preference by similarity to ideal solution (TOPSIS). The results showed that a high dose of TH extract could markedly ameliorate arthritis damage compared to other doses, with flavonoids playing an important role in the antirheumatic activity. The comprehensive quality of samples from Morus alba L. (SS) was superior to those from Liquidambar formosana Hance (FXS). The present study will demonstrate the markers associated with efficacy, and provide an applicable strategy for more comprehensive quality control and evaluation of TH. 相似文献
66.
Pei-Ying Li Jia-Hui Zhao Nian Li Bo Liu Wen-Ge Zhang Zi-Fan Zhu Chao Yan Ning-Lan Xiao Hua-Jie Lai 《Journal of separation science》2022,45(14):2621-2631
Recently, pharmaceuticals and personal care products in the water environment exhibited potential risks to both human and aquatic organisms. In order to improve the sensitivity and accuracy of pharmaceutical detection, the polyimidazolyl acetate ionic liquid was synthesized by Radziszewski reaction and coated on cellulose filter papers as a thin-film extraction phase for extraction of non-steroidal anti-inflammatory drugs from water. The attenuated total reflection-infrared spectrometry, thermogravimetric analysis, and scanning electron microscope analyses demonstrated that the polyimidazolyl acetate ionic liquid was successfully prepared and attached to the surface of the cellulose filter paper through chemical bonding. The adsorption capacity of the homemade thin-film extraction material for the four non-steroidal anti-inflammatory drugs was greater than 8898 ng/cm2 under the optimum conditions, and the desorption rate was over 90%. Then, a paper-based thin-film extraction phase-high-performance liquid chromatography-tandem mass spectrometry method was established for the extraction of non-steroidal anti-inflammatory drugs in water. This method provided limits of detection and limits of quantification were in the range of 0.02–0.15 and 0.17–0.50 μg/L, respectively. Hence, the obtained thin-film extraction phase showed excellent recovery and reproducibility for the target non-steroidal anti-inflammatory drugs with carboxyl groups from water. 相似文献
67.
In this study, α-glucosidase was successfully immobilized on cellulose filter paper and further applied to screening inhibitors from traditional Chinese medicines combined with capillary electrophoresis analysis. For α-glucosidase immobilization, a cellulose filter paper was used as the carrier and grafted with amino groups by coating chitosan, then α-glucosidase was covalently bonded on the amino-modified carrier via epoxy ring-opening reaction using polyethylene glycol diglycidyl ether as the crosslinker. Several parameters influencing the enzyme immobilization were optimized and the optimal values were enzyme concentration of 4 U/mL, polyethylene glycol diglycidyl ether concentration of 1.25%, chitosan concentration of 7.5 mg/mL, immobilization pH 7.0, crosslinking time of 4 h and immobilization time of 2 h. The immobilized α-glucosidase exhibited good batch-to-batch reproducibility (RSD = 2.1%, n = 5), excellent storage stability (73.5% of its initial activity after being stored at 4°C for 15 days), and reusability (75% of its initial activity after 10 repeated cycles). The Michaelis constant of immobilized α-glucosidase and half-maximal inhibitory concentration of acarbose were calculated to be 1.12 mM and 0.38 μM, respectively. Finally, the immobilized α-glucosidase was used for screening inhibitors from 14 kinds of Traditional Chinese Medicine extracts, and Sanguisorbae Radix showed the strongest inhibitory effect on α-glucosidase. 相似文献
68.
The surface analysis of wood and wood products is becoming increasingly important for reasons ranging from the investigation of molecular constituents through to the optimization of industrial processes. As with any natural product, wood analysis is not straightforward, and this review aims to provide guidance for the successful surface analysis of wood by XPS and ToF-SIMS. Through example experiments, three themes are addressed relevant to obtaining meaningful results: considerations related to heterogeneity in the composition of wood (e.g., growth rings); the impact of the chemical removal of minor wood components known as extractives, and whether such a process is necessary; and the potential for misleading or erroneous results as a result of contamination occurring during sample preparation. In addition to discussing successful sample preparation approaches, the important role to be played by MVA in surface analysis is emphasized, particularly in the analysis of ToF-SIMS data. Examples of ToF-SIMS/MVA are provided that highlight the identification of contamination in sample preparation, the quantification of wood composition in terms of cellulose and lignin, and the indication of age of softwood samples. Through consideration of the complexities that influence wood surface analysis, the design and interpretation of consequential experiments become easier and more accurate. 相似文献
69.
Precise determination of d-spacings and compositional ratio of cellulose Iα and Iβ in various native cellulose samples was successfully carried out by synchrotron-radiated X-ray diffraction and time-of-flight
(TOF) neutron diffraction from quasi-powder specimens. X-ray diffraction peaks were separated by the deconvolution method
using six types of profile function: Gaussian, Lorentzian, intermediate Lorentzian, modified Lorentzian, pseudo-Voigt, and
Pearson VII. In terms of R-factors, the pseudo-Voigt function gave the best fit with the observation, and was used for determination
of d-spacings. The numerical results for Valonia cellulose were: dIα (1 0 0) = 0.613 nm; dIβ (1 1 0) = 0.603 nm; dIβ (1 1 0) = 0.535 nm; dIα (0 1 0) = 0.529 nm; Iα content = 0.65. The differences determined between dIα (1 0 0) and dIβ (1 1 0) and between dIβ (1 1 0) and dIα (0 1 0) were similar to those previously reported. Comparison between unresolved peaks for the two types of cellulose samples
revealed a small but definite difference between dIα (1 1 0) and dIβ (2 0 0). The TOF neutron diffractometry using deuterated samples confirmed this difference.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
70.
The preparation of polymer microcapsules of well defined size in the range of 10–50 μm with different shell thickness to
core diameter ratios is described. An aerosol of monodisperse droplets of a homogeneous ternary liquid system which contained
a hydrophobic component and a hydrophilic component dissolved in a high-volatile mutual solvent, was produced by dispersing
with a vibrating-orifice aerosol generator. After the evaporation of the solvent in a nitrogen atmosphere the particles demix
and form a two-phase droplet of core-shell type. These droplets were illuminated with UV light and polymerized to highly monodisperse
microcapsules with a solid polymer shell and a liquid core. The properties of the resulting particles (size, size distribution,
shell thickness, shape and surface characteristics) were investigated by scanning electron microscopy, Raman spectroscopy
on single optically levitated particles, and confocal Raman micro spectroscopy. The microcapsules were highly monodisperse
and have spherical shape.
Received: 24 July 1996 Accepted: 29 August 1996 相似文献