全文获取类型
收费全文 | 6757篇 |
免费 | 809篇 |
国内免费 | 1813篇 |
专业分类
化学 | 5334篇 |
晶体学 | 186篇 |
力学 | 1363篇 |
综合类 | 85篇 |
数学 | 554篇 |
物理学 | 1857篇 |
出版年
2024年 | 17篇 |
2023年 | 131篇 |
2022年 | 214篇 |
2021年 | 239篇 |
2020年 | 308篇 |
2019年 | 272篇 |
2018年 | 241篇 |
2017年 | 368篇 |
2016年 | 362篇 |
2015年 | 289篇 |
2014年 | 384篇 |
2013年 | 647篇 |
2012年 | 422篇 |
2011年 | 482篇 |
2010年 | 360篇 |
2009年 | 453篇 |
2008年 | 451篇 |
2007年 | 478篇 |
2006年 | 433篇 |
2005年 | 408篇 |
2004年 | 367篇 |
2003年 | 301篇 |
2002年 | 250篇 |
2001年 | 251篇 |
2000年 | 223篇 |
1999年 | 182篇 |
1998年 | 149篇 |
1997年 | 145篇 |
1996年 | 104篇 |
1995年 | 89篇 |
1994年 | 85篇 |
1993年 | 65篇 |
1992年 | 49篇 |
1991年 | 31篇 |
1990年 | 25篇 |
1989年 | 20篇 |
1988年 | 15篇 |
1987年 | 17篇 |
1986年 | 13篇 |
1985年 | 9篇 |
1984年 | 8篇 |
1983年 | 2篇 |
1982年 | 4篇 |
1980年 | 1篇 |
1979年 | 7篇 |
1978年 | 1篇 |
1977年 | 2篇 |
1976年 | 1篇 |
1971年 | 1篇 |
1957年 | 2篇 |
排序方式: 共有9379条查询结果,搜索用时 248 毫秒
991.
Amara Venkateswara Rao Basa Ashok Gopireddy Venkata Subbareddy Vatti Chandra Sekhar Gollapudi Venkata Ramanamurthy 《International Journal of Polymer Analysis and Characterization》2019,24(4):346-354
Using aqueous extraction of red sanders powder as a reducing agent, silver and copper bimetallic nanoparticles were in situ generated in cotton fabrics. Silver and copper nanoparticles were also generated separately for comparison. The resulted nanocomposite cotton fabrics (NCFs) were characterized by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and antibacterial tests. SEM analysis indicated the generation of more number of nanoparticles when bimetallic source solutions were used. Further, the size range of the generated bimetallic nanoparticles was found to be lower than when individual metal nanoparticles were generated in NCFs. XRD analysis confirmed the in situ generation of silver and copper nanoparticles when equimolar bimetallic salt source solutions were utilized. The NCFs with bimetallic nanoparticles exhibited higher antibacterial activity against both Gram-negative and Gram-positive bacteria and hence can be considered for applications as antibacterial bed and dressing materials. 相似文献
992.
Jianglong Duan Tianlong Huang Wenjuan Liu Yanmin Zhao Wei Wu 《International Journal of Polymer Analysis and Characterization》2019,24(5):428-438
Three-dimensional biodegradable porous scaffolds play an important role in tissue engineering. The degradable scaffold material, based on 1,4-butanediamine-modified poly(lactide-co-glycolide) (BMPLGA), nano-bioactive glass (NBAG), and nano-β-tricalciumphosphate (β-TCP), was prepared by a solution-casting/salt-leaching method. The biological properties were studied by using cell cytotoxicity, von Kossa staining, alkaline phosphatase activity, hemolytic test, acute toxicity, and genetic toxicity test. The MTT results indicated that the BMPLGA/NBAG-β-TCP materials did not show any cytotoxicity. The result of von Kossa staining showed that the introduction of the NBAG and β-TCP promoted fibroblastic differentiation and improved the mineral deposition of the BMPLGA matrix. In addition, the presence of NBAG and β-TCP in the composite further enhanced the ALP activity in comparison with the sole BMPLGA material. The hemolytic potential showed that the nanocomposite scaffolds were non-hemolytic. The BMPLGA/NBAG-β-TCP scaffolds showed no acute systemic toxicity or mutagenic action. Therefore, the results indicated the BMPLGA/NBAG-β-TCP nanocomposite scaffold could be considered as a potential bone tissue engineering implant. 相似文献
993.
This study presents a sensitive voltammetric determination of terbutaline (TER) on a platform based on carbon nanotubes (CNTs) and europium oxide nanoparticles (Eu2O3NPs) coated glassy carbon electrodes (GCEs). An ultrasonic bath was performed for the preparation of composite material. The material was characterized by energy dispersive X‐ray spectroscopy (EDX), X‐ray diffraction method (XRD) and scanning electron microscopy (SEM). The Eu2O3NPs/CNTs/GCE system was assessed for the oxidation of terbutaline (TER). A broad oxidation peak was appeared at 0.71 V using a bare GCE. However, the voltammetry of TER has been improved at a GCE coated with CNTs and a well‐defined anodic peak exhibited at 0.61 V. Furthermore, the nanoparticles of Eu2O3 and CNTs coated GCE has greatly improved the electrochemical behaviour of TER and a sharp peak was appeared at 0.59 V. Cyclic voltammetry at Eu2O3NPs/CNTs/GCE also reveals a high catalytic effect for the oxidation of TER with an oxidation peak that is distinctly enhanced compared to GCE and CNTs/GCE. Eu2O3 nanoparticles were utilized to enhance the surface area of GCE and then improve the sensitivity of the procedure. The response of TER was linear over a concentration range of 2.0×10?8 M ?9.5×10?6 M with an LOD of 3.7×10?9 M. Square wave voltammetric analysis of tablets by Eu2O3NPs/CNTs/GCE yielded a recovery of 99.2 % with an RSD% of 3.2. The modified electrode (EuO2NPs/CNTs/GCE) provides accuracy and precision to the analysis of samples. 相似文献
994.
The composite of carbon nanotube (CNT) and phenolic resin was prepared in a piece of fused silica capillary based on the far infrared‐assisted crosslinking of phenolic novolac resin in the presence of CNTs and hexamethylenetetramine for electrochemical sensing. The surface morphology and structure of the prepared materials were investigated by scanning electron microscopy, energy dispersive X‐ray spectroscopy and Fourier transform infrared spectroscopy. The results indicated that CNTs in the composite was adhered by the crosslinked phenolic resin to form an electrically conductive network. Many broken ends of CNTs appeared on the surface of the composite electrode in the form of a nanoelectrode array. The novel electrode was employed in the amperometric detection of synephrine and hesperidin in Citri Reticulatae Pericarpium in combination with capillary zone electrophoresis. The novel CNT‐based electrode owned the advantages of high sensitivity, low fabrication expense and excellent electrocatalytic performances, indicating great promise for the electrochemical detection in other analysis systems. 相似文献
995.
The present work reports a simple and single‐step hydrothermal synthesis of MoSe2?MoO3 composite for highly sensitive and selective electrochemical oxidation of nitrite. FESEM of the MoSe2?MoO3 hybrid revealed the formation of composite as laminated structure of different sizes piled up together as finger‐like MoSe2 bars whilst other physico‐chemical characterizations (XRD, FTIR, UV‐Vis, XPS) confirmed that co‐existence of MoO3 as a major by‐product of hydrothermal synthesis. The as‐fabricated MoSe2?MoO3 composite based nitrite sensor showed remarkable selectivity and reproducibility with <3s of response time, excellent sensitivity and detection limit of 10.84 A M?1 cm?2 (R2=0.996) and 0.1 μM, respectively, in the range of 2.5–80 μM. The obtained sensitivity can be credited to the high surface area obtained from 1T phase MoSe2 and α phase MoO3 as the sensing material. The developed sensor was effectively evaluated for electrochemical recognition of nitrite in the water samples (potable and tap water) gathered from an industrial area. This new and efficient MoSe2?MoO3 based electrode material offers a new frontier for the progress of a novel composites by simple and single‐step approach which can be used for progress of non‐enzymatic and inexpensive electrochemical sensors for a wide range of analytical applications. 相似文献
996.
In situ forming implants (ISFIs) appear to be a convenient drug delivery system, alternative to conventional preformed implants and microparticles for parenteral drug delivery applications. It has been shown that they offer several advantages including easy and minimally invasive application, potential for local/site‐specific drug delivery that allows reduction of side effects associated with systemic administration of drug. A few ISFI formulations based on poly(α‐hydroxy acids), solidifying by solid phase separation, are currently commercially available. In this work, polyesters based on sebacic acid, isosorbide, and optionally 1,2‐propanediol were synthesized and characterized. Poly(isosorbide sebacate‐co‐1,2‐propylene sebacate) (PISEBPG) was chosen as an essential constituent of new ISFI formulations dedicated to controlled release of doxycycline hyclate (DOXY). Basic characteristics of new ISFI formulations were investigated. In particular, the influence of addition of a relatively hydrophobic cosolvent (triacetin, TA) to a more hydrophilic 1‐methyl‐2‐pyrrolidone (NMP) as well as the presence of calcium carbonate (CAC) on the morphology of resulted depots and DOXY release profile was evaluated. Scanning electron microscopy (SEM) analysis revealed that the presence of TA resulted in more porous morphology of the depots. DOXY has been releasing continuously from depots in vitro within 12 weeks depending on the composition. The release profile of the PISEBPG‐based formulation containing CAC indicates that it could be useful where short‐term (up to 14 d), rapid release of the antibiotic is required, while formulation without CAC, where after 21 days about 50% of the drug loaded may still be available for release, may be better for the long‐term delivery of DOXY. 相似文献
997.
The vinyl group terminated water-borne polyurethanes (WPU) with different DMPA content were prepared. Subsequently the core-shell polyurethane/polyacrylate (PUA) composite emulsions were synthesized by soap-free emulsion copolymerization. The WPU as sole surfactant was used in copolymerization, and the lowest surface tension could be achieved to 38.8?mN m?1. Furthermore, the final conversion of acrylic monomer was reached to 98% in the case of WPU reactive seed. The FTIR-ATR indirectly confirmed the core-shell structure of PUA, simultaneously combined with DSC results found that the compatibility of WPU and PA was enhanced by growing grafting efficiency. The TEM results further indicated that the amount of DMPA in WPU had a great significant role in polymerization and final morphology structure. The PUA composite particles changed from scattered structure, core-shell structure to multi-core structure with increasing DMPA content. Correspondingly, the reinforcing and toughening effects were also found in PUA films with the increase content of DMPA by tensile testing. 相似文献
998.
Audra M. Judd Danielle B. Gutierrez Jessica L. Moore Nathan Heath Patterson Junhai Yang Carrie E. Romer Jeremy L. Norris Richard M. Caprioli 《Journal of mass spectrometry : JMS》2019,54(8):ii-ii
Matrix‐assisted laser desorption/ionization imaging mass spectrometry (MALDI IMS) is a molecular imaging technology uniquely capable of untargeted measurement of proteins, lipids, and metabolites while retaining spatial information about their location in situ. This powerful combination of capabilities has the potential to bring a wealth of knowledge to the field of molecular histology. Translation of this innovative research tool into clinical laboratories requires the development of reliable sample preparation protocols for the analysis of proteins from formalin‐fixed paraffin‐embedded (FFPE) tissues, the standard preservation process in clinical pathology. Although ideal for stained tissue analysis by microscopy, the FFPE process cross‐links, disrupts, or can remove proteins from the tissue, making analysis of the protein content challenging. To date, reported approaches differ widely in process and efficacy. This tutorial presents a strategy derived from systematic testing and optimization of key parameters, for reproducible in situ tryptic digestion of proteins in FFPE tissue and subsequent MALDI IMS analysis. The approach describes a generalized method for FFPE tissues originating from virtually any source. 相似文献
999.
Ali M. Abdel‐Mageed Alexander Klyushin Azita Rezvani Axel Knop‐Gericke Robert Schlgl R. Jürgen Behm 《Angewandte Chemie (International ed. in English)》2019,58(30):10325-10329
The electronic and structural properties of Au/ZnO under industrial and idealized methanol synthesis conditions have been investigated. This was achieved by kinetic measurements in combination with time‐resolved operando infrared (DRIFTS) as well as in situ near‐ambient pressure X‐ray photoelectron spectroscopy (NAP‐XPS) and X‐ray absorption near‐edge spectroscopy (XANES) measurements at the O K‐edge together with high‐resolution electron microscopy. The adsorption of CO during the reaction revealed the presence of negatively charged Au nanoparticles/Au sites during the initial phase of the reaction. Near‐ambient‐pressure XPS and XANES demonstrate the build‐up of O vacancies during the reaction, which goes along with a substantial increase in the rate of methanol formation. The results are discussed in comparison with previous findings for Cu/ZnO and Au/ZnO catalysts. 相似文献