全文获取类型
收费全文 | 2141篇 |
免费 | 59篇 |
国内免费 | 2篇 |
专业分类
化学 | 1417篇 |
晶体学 | 21篇 |
力学 | 58篇 |
数学 | 299篇 |
物理学 | 407篇 |
出版年
2023年 | 14篇 |
2022年 | 55篇 |
2021年 | 77篇 |
2020年 | 38篇 |
2019年 | 48篇 |
2018年 | 44篇 |
2017年 | 43篇 |
2016年 | 79篇 |
2015年 | 64篇 |
2014年 | 86篇 |
2013年 | 129篇 |
2012年 | 141篇 |
2011年 | 170篇 |
2010年 | 104篇 |
2009年 | 133篇 |
2008年 | 163篇 |
2007年 | 125篇 |
2006年 | 107篇 |
2005年 | 76篇 |
2004年 | 72篇 |
2003年 | 57篇 |
2002年 | 48篇 |
2001年 | 40篇 |
2000年 | 30篇 |
1999年 | 20篇 |
1998年 | 29篇 |
1997年 | 14篇 |
1996年 | 22篇 |
1995年 | 23篇 |
1994年 | 14篇 |
1993年 | 13篇 |
1992年 | 13篇 |
1991年 | 9篇 |
1989年 | 8篇 |
1988年 | 4篇 |
1987年 | 3篇 |
1986年 | 5篇 |
1985年 | 11篇 |
1984年 | 5篇 |
1983年 | 8篇 |
1982年 | 5篇 |
1981年 | 12篇 |
1980年 | 4篇 |
1979年 | 4篇 |
1978年 | 5篇 |
1976年 | 8篇 |
1974年 | 3篇 |
1902年 | 2篇 |
1897年 | 2篇 |
1894年 | 2篇 |
排序方式: 共有2202条查询结果,搜索用时 31 毫秒
101.
Hugo R. Fernandes Dilshat U. Tulyaganov José M. F. Ferreira 《Journal of Thermal Analysis and Calorimetry》2013,112(3):1359-1368
The crystallisation kinetics of experimental glasses in 3 different systems: (A) Li2O–SiO2, (B) Li2O–Al2O3–SiO2 and (C) Li2O–K2O–Al2O3–SiO2 were studied under non-isothermal conditions. The DTA results revealed a stronger tendency to crystallisation of binary compositions in comparison to the ternary and quaternary compositions comprising Al2O3 and K2O which present the lower crystallisation, i.e. the crystallisation propensity follows the trend A > B > C. The devitrification process in the Li2O–SiO2 and Li2O–Al2O3–SiO2 systems began earlier and the rate was higher in comparison to that of glasses in the quaternary Li2O–K2O–Al2O3–SiO2 system. Thus, addition of Al2O3 and K2O to glasses of Li2O–SiO2 system was demonstrated to promote glass stability against crystallisation. However, the activation energy for crystallisation was shown to depend also on the SiO2/Li2O ratio with the binary system showing a decreasing trend with increasing SiO2/Li2O ratio, while the opposite tendency was being observed for compositions with added Al2O3 and K2O. 相似文献
102.
Brenno Santos Leite Melissa Tatiana Andreuccetti Sibele Augusta Ferreira Leite José Vicente Hallak d’Angelo 《Journal of Thermal Analysis and Calorimetry》2013,112(3):1539-1544
As a consequence of the continuous increase in the production rate of pulp and paper mills around the world, a great quantity of black liquor, a by-product of the wood digestion process, is produced. This by-product has a great potential as biomass, but needs to be concentrated to higher solids content to be burned as fuel in a recovery boiler. This is necessary to make the pulping process economically feasible, incinerating black liquor to produce high pressure steam, recycling inorganic chemicals to the process. The greater the solids content in black liquor, the better the combustion process in the boiler. Nevertheless, concentration of solids in black liquor above 75 mass/%, causes scaling formation on the heat transfer surfaces of evaporators and concentrators, due to the precipitation of sodium salts, reducing the overall efficiency of this equipment. The aim of this work is to evaluate the use of thermal analyses techniques, TG and DSC, as alternative methods to estimate solids content in eucalyptus black liquor samples since this information is essential to understand scaling formation process, allowing actions to reduce this industrial problem. Traditional techniques applied to determine solids content use gravimetric methods, which are simple, fine, but take a lot of time to be executed. Thermal analyses have proved to be very accurate and have the advantage to be faster than the traditional techniques. On the other hand, the cost-benefit relationship of the traditional technique is much greater and the final decision which one should be used depends on the conditions available. 相似文献
103.
D. A. L. Almeida E. F. Antunes V. Q. da Silva M. R. Baldan N. G. Ferreira 《Journal of Solid State Electrochemistry》2013,17(7):1977-1984
Composite electrodes of vertically aligned carbon nanotubes (VACNT) were synthesized on carbon fiber (CF) substrate by pyrolysis of camphor/ferrocene using a SiO2 interlayer as a barrier against metal diffusion into the substrate. Two treatments were used to remove iron from CF/VACNT structure: thermal annealing at high temperature under inert atmosphere and electrochemical oxidation in H2SO4 solution. The composites were characterized by scanning electron microscopy and Raman scattering spectroscopy. Besides, the electrochemical behavior of CF/VACNT was analyzed by cyclic voltammetry and charge/discharge tests. CF/VACNT composite submitted to the electrochemical oxidation showed the best electrochemical performance, with high specific capacitance, which makes it very attractive as electrode for supercapacitors. 相似文献
104.
105.
Patrícia Santiago de Oliveira Patricio Iaci Miranda Pereira Natália Cristina Ferreira da Silva Eliane Ayres Fabiano Vargas Pereira Rodrigo Lambert Oréfice 《European Polymer Journal》2013
Polyurethane waterborne synthesis was performed using a two-step method, commonly referred to as a prepolymer method. Nanocomposites based on waterborne polyurethane and cellulose nanocrystals were prepared by the prepolymer method by altering the mode and step in which the nanofillers were incorporated during the polyurethane formation. The morphology, structural, thermal, and mechanical properties of the resulting nanocomposite films were evaluated by Fourier transform infrared spectroscopy (FTIR), small angle X-ray scattering (SAXS), scanning electron microscopy (SEM), and tensile tests. FTIR results indicated that the degree of interaction between the nanofillers and the WPU through hydrogen bonds could be controlled by the method of cellulose nanocrystal incorporation. Data obtained from SAXS experiments showed that the cellulose nanocrystals as well as the step of the reaction in which they are added influenced the morphology of the polyurethane. The reinforcing effect of CNCs on the nanocomposites depends on their morphology. 相似文献
106.
M. H. Godinho C. Cruz P. I. C. Teixeira A. J. Ferreira C. Costa P. S. Kulkarni 《Liquid crystals》2013,40(2):103-107
The phase behaviour of a number of N‐alkylimidazolium salts was studied using polarizing optical microscopy, differential scanning calorimetry and X‐ray diffraction. Two of these compounds exhibit lamellar mesophases at temperatures above 50°C. In these systems, the liquid crystalline behaviour may be induced at room temperature by shear. Sheared films of these materials, observed between crossed polarisers, have a morphology that is typical of (wet) liquid foams: they partition into dark domains separated by brighter (birefringent) walls, which are approximately arcs of circle and meet at “Plateau borders” with three or more sides. Where walls meet three at a time, they do so at approximately 120° angles. These patterns coarsen with time and both T1 and T2 processes have been observed, as in foams. The time evolution of domains is also consistent with von Neumann's law. We conjecture that the bright walls are regions of high concentration of defects produced by shear, and that the system is dominated by the interfacial tension between these walls and the uniform domains. The control of self‐organised monodomains, as observed in these systems, is expected to play an important role in potential applications. 相似文献
107.
Thiago Henrique Napoleão Teodomiro Gomes dos Santos-Filho Emmanuel Viana Pontual Rodrigo da Silva Ferreira Luana Cassandra Breitenbach Barroso Coelho Patrícia Maria Guedes Paiva 《Applied biochemistry and biotechnology》2013,171(3):744-755
This work reports the use of matrices containing Cratylia mollis lectins (Cramoll 1,2,3-Sepharose and Cramoll 3-Sepharose) for isolation of glycoproteins from fetal bovine serum, human colostrum, hen egg white, and human blood plasma. Cramoll 1,2,3-Sepharose was able to bind a glycoprotein from fetal bovine serum which showed the same fetuin electrophoretic profile. The data indicate that this protein adsorbed to the matrix by interaction with Cramoll 3. Cramoll 1,2,3-Sepharose was not efficient to retain glycoproteins from human colostrum or commercial ovalbumin. Cramoll 3-Sepharose bound ovalbumin, and the support retained protein from hen egg white. Protein peaks eluted from the column with 1.0 M NaCl or 0.3 M galactose showed apparent molecular mass of ovalbumin. Two main proteins from blood plasma with apparent molecular mass 67 (similar to albumin) and 50 kDa (similar to fetuin) adsorbed on Cramoll 3-Sepharose and were eluted with 1.0 M NaCl as a single peak. Elution of adsorbed plasma proteins with 0.3 M galactose was less selective than with 1.0 M NaCl as revealed by SDS-PAGE. In conclusion, the Cramoll 1,2,3-Sepharose and Cramoll 3-Sepharose matrices were useful to separate glycoproteins from complex protein mixtures, and the adsorption phenomena was a carbohydrate-dependent event. 相似文献
108.
Gabriel G.A. de Carvalho Mário A. Feres Jr José R. Ferreira Valerie H. Kennedy 《International journal of environmental analytical chemistry》2013,93(9):686-696
A simple and reliable method for Hg determination in fish samples has been developed. Lyophilised fish tissue samples were extracted in a 25% (w/v) tetramethylammonium hydroxide (TMAH) solution; the extracts were then analysed by FI-CVAFS. This method can be used to determine total and inorganic Hg, using the same FI manifold. For total Hg determination, a 0.1% (w/v) KMnO4 solution was added to the FI manifold at the sample zone, followed by the addition of a 0.5% (w/v) SnCl2 solution, whereas inorganic Hg was determined by adding a 0.1% (w/v) L-cysteine solution followed by a 1.0% (w/v) SnCl2 solution to the FI system. The organic fraction was determined as the difference between total and inorganic Hg. Sample preparation, reagent consumption and parameters that can influence the FI-CVAFS performance were also evaluated. The limit of detection for this method is 3.7 ng g?1 for total Hg and 4.3 ng g?1 for inorganic Hg. The relative standard deviation for a 1.0 µg L?1 CH3Hg standard solution (n = 20) was 1.1%, and 1.3% for a 1.0 µg L–1 Hg2+ standard solution (n = 20). Accuracy was assessed by the analysis of Certified Reference Material (dogfish: DORM-2, NRCC). Recoveries of 99.1% for total Hg and 93.9% inorganic Hg were obtained. Mercury losses were not observed when sample solutions were re-analysed after a seven day period of storage at 4°C. 相似文献
109.
Walter N. L. dos Santos Dannuza D. Cavalcante Hadla S. Ferreira Cesário F. das Virgens Aline R. Borges Marcia M. Silva 《International journal of environmental analytical chemistry》2013,93(15):1447-1452
A cloud point extraction procedure for pre-concentration and determination of cadmium and lead in drinking water using sequential multi-element flame atomic absorption spectrometry is described. 4-(2-thiazolylazo)-orcinol (TAO) has been used as complexing agent and the micellar phase was obtained using the non-ionic surfactant octylphenoxypolyethoxyethanol (Triton X-114) and centrifugation. The conditions for reaction and extraction (surfactant concentration, reagent concentration, effect of incubation time, etc) were studied and the analytical characteristics of the method were determined. The method allows the determination of cadmium and lead with quantification limits of 0.30?µg?L?1 and 2.6?µg?L?1, respectively. A precision expressed as relative standard deviation (RSD, n?=?10) of 2.3% and 2.6% has been obtained for cadmium concentrations of 10?µg?L?1 and 30?µg?L?1, respectively, and RSD of 1.3% and 1.7% for lead concentrations of 10?µg?L?1 and 30?µg?L?1, respectively. The accuracy was confirmed by analysis of a natural water certified reference material. The method has been applied for the determination of cadmium and lead in drinking water samples collected in the cities of Ilhéus and Itabuna, Brazil. Recovery tests have also been performed for some samples, and results varied from 96 to 105% for cadmium and 97 to 106% for lead. The cadmium and lead concentrations found in these samples were always lower than the permissible maximum levels stipulated by World Health Organization and the Brazilian Government. 相似文献
110.
Celso Santi Junior Adriane Maria Ferreira Milagres André Ferraz Walter Carvalho 《Cellulose (London, England)》2013,20(6):3165-3177
The porosity of lignocellulosic materials is a key feature for the enzymatic hydrolysis of the constituent polysaccharides, being affected by its drying and lignin content. Here we evaluated the influence of both parameters in the porosity of sugarcane bagasse, using raw and chlorite-delignified samples. A fraction of these samples was air dried at room temperature and the remainder one was kept wet. All the samples were subjected to porometry (solute exclusion technique), determination of water retention value and assessment of enzymatic saccharification of polysaccharides. Samples with higher lignin contents had lower porosities and exhibited worse enzymatic conversions of polysaccharides. Mild drying collapsed only the smaller pores, which already were inaccessible to enzymes, and therefore did not affect the efficiencies of saccharification. Our results show that the lignin content plays an important role in the porosity of the material and that its removal improves the enzymatic saccharification of the constituent polysaccharides. 相似文献