全文获取类型
收费全文 | 7555篇 |
免费 | 533篇 |
国内免费 | 993篇 |
专业分类
化学 | 7619篇 |
晶体学 | 80篇 |
力学 | 97篇 |
综合类 | 41篇 |
数学 | 49篇 |
物理学 | 1195篇 |
出版年
2024年 | 16篇 |
2023年 | 58篇 |
2022年 | 151篇 |
2021年 | 184篇 |
2020年 | 204篇 |
2019年 | 189篇 |
2018年 | 126篇 |
2017年 | 152篇 |
2016年 | 261篇 |
2015年 | 234篇 |
2014年 | 234篇 |
2013年 | 667篇 |
2012年 | 318篇 |
2011年 | 358篇 |
2010年 | 310篇 |
2009年 | 379篇 |
2008年 | 479篇 |
2007年 | 541篇 |
2006年 | 465篇 |
2005年 | 428篇 |
2004年 | 411篇 |
2003年 | 350篇 |
2002年 | 288篇 |
2001年 | 245篇 |
2000年 | 264篇 |
1999年 | 239篇 |
1998年 | 190篇 |
1997年 | 221篇 |
1996年 | 187篇 |
1995年 | 184篇 |
1994年 | 161篇 |
1993年 | 141篇 |
1992年 | 150篇 |
1991年 | 65篇 |
1990年 | 39篇 |
1989年 | 32篇 |
1988年 | 38篇 |
1987年 | 16篇 |
1986年 | 18篇 |
1985年 | 18篇 |
1984年 | 12篇 |
1983年 | 5篇 |
1982年 | 12篇 |
1981年 | 10篇 |
1980年 | 8篇 |
1978年 | 3篇 |
1977年 | 3篇 |
1976年 | 4篇 |
1974年 | 3篇 |
1973年 | 3篇 |
排序方式: 共有9081条查询结果,搜索用时 15 毫秒
181.
Two different methods to graft silica particles with poly(acrylic acid) (PAA) were studied. In the first method PAA was reacted with 1,1′‐carbonyldiimidazole to give functionalized PAA. The resulting activated carbonyl group reacted easily with 3‐aminopropyl‐functionalized silica at low temperatures. In the second method 3‐glycidoxypropyl‐functionalized silica particles were reacted directly with PAA by using magnesium chloride as a catalyst. Different molecular weights of PAAs were used in order to investigate the effect of molecular weight on grafting yields in both methods. The grafting yields were determined with thermogravimetric analysis (TGA). All products were also investigated with IR. The results showed that the yields of reactions performed at ambient temperature by using 1,1′‐carbonyldiimidazole‐functionalized PAA were the same as with a direct reaction of unfunctionalized PAA and 3‐aminopropyl‐functionalized silica performed at 153°C. Also in reactions between 3‐glycidoxypropyl‐functionalized silica and PAA the yields were satisfactory. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
182.
Cd2+ complexes with antibiotics viz. neomycin, chlortetracycline, oxytetracycline, tetracycline, penicillin‐V and penicillin‐G as primary ligands and vitamin‐B5 as secondary ligand have been reported at pH = 7.30 ± 0.01 and μ = 1.0 M KNO3 at 298 K by polarographic technique.1 Cd2+ formed 1:1:1, 1:1:2, and 1:2:1 complexes with a stability constants trend of neomycin < chlortetracycline < oxytetracycline < tetracycline < penicillin‐V < penicillin‐G can be explained on the basis of the nature of ligands, bonding, and steric hindrance of these drugs. The nature of electrode processes were reversible and diffusion controlled. The values of stability constants showed that these drugs can be used to reduce the toxicity of Cd. 相似文献
183.
Cestari AR Vieira EF Dos Santos AG Mota JA de Almeida VP 《Journal of colloid and interface science》2004,280(2):380-386
In this work, chitosan beads were synthesized in acidic medium and cross-linked in 1% glutaraldehyde solution. The characterization of the materials using TG/DTG, XRD, and BET surface areas showed that the beads did not modify their characteristics after the cross-linking reaction. The cross-linked beads were utilized as adsorbents for the removal of the yellow-, blue-, and red-anionic reactive dyes from aqueous solutions at pH 2.0. Adsorption of the yellow-dye increased from 25 to 50 degrees C. However, adsorption of the blue-dye decreased from 25 to 50 degrees C. Interestingly, the adsorption of the red-dye decreased from 25 to 35 degrees C and increased from 45 to 50 degrees C. The kinetic data were evaluated using an Avrami kinetic model, where the parameter n was related to the determination of changes in the adsorption mechanisms. Adsorption data of the dyes in relation to the contact time, the chemical structures of the dyes, and temperature were presented and were discussed. 相似文献
184.
Johannes Smid 《Journal of polymer science. Part A, Polymer chemistry》2004,42(15):3655-3667
The discovery and implications of the existence of two kinds of ion pairs in solutions of carbanion salts is described. Also discussed are the factors controlling tight–loose ion pair equilibrium: the nature of the carbanion and its counterion, temperature, pressure, solvent, and cation‐complexing additives. A few examples are presented of the effect of these ionic species on the mechanisms of anionic polymerization and proton transfer. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3655–3667, 2004 相似文献
185.
Effect of multi-walled carbon nanotubes on non-isothermal crystallization kinetics of polyamide 6 总被引:2,自引:0,他引:2
The non-isothermal crystallization behaviors of multi-walled carbon nanotubes (MWNTs)/polyamide 6 (PA6) composites were investigated by differential scanning calorimetry (DSC). Three methods, namely, Avrami, Ozawa and Mo, were carried out to analyze the non-isothermal crystallization data. The results showed that the MWNTs in PA6 acted as effective nucleation agents. However the crystallization rate of composites obtained was lower than that of the neat PA6. It is indicated that the presence of MWNTs influenced the mechanism of nucleation and the growth of PA6 crystallites. 相似文献
186.
《Arabian Journal of Chemistry》2022,15(7):103900
Emerging pharmaceutical ingredients (APIs) like sulfamethoxazole (SMX), metronidazole (MNZ) and ciprofloxacin (CIP) are biopersistent and toxic to the environment and public health. In this study, UV/TiO2 photodegradation was applied in the degradation of SMX, MNZ and CIP individually and in a mixture. For a 5 mg/L SMX solution, about 97% of SMX was degraded within 360 min, which was reduced to 80% for 80 mg/L of SMX solution at the same TiO2 dosage and photodegradation time. The maximum removals of MNZ and CIP as individual components were 100% and 89%, respectively at 600 min of photodegradation reaction time. For binary mixtures, the highest removal (100%) was achieved for MNZ and CIP ([MNZ] = [CIP] = 40 mg/L) mixture at 120 min whereas the degradations were 97% and 96% for SMX and MNZ, and SMX and CIP binary mixtures, respectively, even after 600 min of experimental time at the same concentrations. For tertiary mixture, the maximum degradation 99% was observed for (SMX = CIP] = 20 mg/L and [MNZ] = [40 mg/L) at 600 min. The observed reaction rate was 0.01085 min?1 when SMX concentration was 5 mg/L, which decreased to 0.00501 min?1 for SMX concentration of 80 mg/L, indicating decreasing of reaction rate at higher concentration. The results indicate that the UV/TiO2 process is promising to apply for the treatment of pharmaceutical wastewaters. 相似文献
187.
D. V. Kazakov D. R. Khusnullina N. N. Kabal'nova S. L. Khursan V. V. Shereshovets 《Russian Chemical Bulletin》1997,46(10):1690-1693
The kinetics of the reaction between dimethyldioxirane and 2-methylbutane in acetone solutions were studied spectrophotometrically
at 25 °C. The radical-chain induced decomposition of dioxirane proceeding with the participation of the carbon-centered radicals
follows the first-order kinetic law. The reaction is inhibited by dioxygen. In the presence of O2, the dimethyldioxirane consumption is due to the homolysis of the O−O bond (at a rate constant of 6.3·10−4 s−1) followed by attack of the C−H bond of 2-methylbutane by the biradical formed. The rate constant of the reaction between
the alkyl radical and dimethyldioxirane was estimated.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1785–1788, October, 1997. 相似文献
188.
The studies were devoted to determination of the effect of gas atmosphere and its pressure on the second step of decomposition
of hydrated titanium dioxide (HTD) promoted by sulfate groups.
It has been found that thermal decomposition of HTD at temperatures above 300°C consists of a number of processes such as
dehydroxylation, desulfuration, recrystallization and sintering of solid grains, photochemical processes (if the decomposition
proceeds in the presence of light) and adsorption of gas phase components (in the presence of air or SO2).
Kinetic parameters characterizing this step of decomposition have been determined for processes carried out in vacuum and
in argon or air atmospheres (at a pressure of 13.33hPa). The kinetic curves of decomposition carried out in the presence of
gases capable of being adsorbed on the surface of partly dehydrated HTD are featured by local extrema due to simultaneous
processes of decomposition and adsorption of gas components.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
189.
Kang De Yao Tao Peng Han Bao Feng Yu Ying He 《Journal of polymer science. Part A, Polymer chemistry》1994,32(7):1213-1223
The aqueous swelling kinetics of a series of crosslinked chitosan (cr-CS) with glutaraldehyde (GA) interpenetrating polyether hydrogels have been studied as functions of pH, the N-deacetylation degree of chitosan, the amount of crosslinking agent, the electrolyte composition in solution, temperature, and gel composition. Based on these results, the swelling mechanism of the hydrogels was discussed. The release profiles of chlorhexidini acetas from the semi-IPN were also investigated. © 1994 John Wiley & Sons, Inc. 相似文献
190.
D. M. Petrović-Djakov J. M. Filipović Lj. P. Vrhovac J. S. Veličković 《Journal of Thermal Analysis and Calorimetry》1996,46(6):1681-1686
The kinetics of the AIBN-initiated free radical bulk polymerization of fiveo-alkylphenyl methacrylates was studied by means of DSC in the temperature range 353–373 K, and the enthalpy of polymerization, the overall reaction rate constant and the activation energy were determined. The results were compared with those published recently on correspondingp-alkylaryl methacrylates. All measured reaction rate constants were found to increase with increasing temperature and to decrease with increasingo-alkyl substituent mass and size. It was shown thato-substituents influence the rates of polymerization to a greater extent thanp-substituents. At about 373 K, all differences in rate, most probably resulting from steric hindrance caused by the alkyl groups, disappear in both series, a phenomenon earlier observed for dimethyl phenyl methacrylates.This work was supported by the Ministry of Science of the Republic of Serbia. 相似文献