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971.
通过电化学原位聚合法制备多孔网状结构的聚苯胺(PANI)/醋酸纤维素(CA)复合膜电极,该复合膜的内层(与电极接触的一面)呈墨绿色,外层呈白色。采用原子力显微镜(AFM)、扫描电镜(SEM)、红外光谱(FTIR)对其形貌和化学组成进行表征。通过循环伏安、恒电流充放电和电化学阻抗研究了复合膜电极的超级电容特性。结果表明,多孔网状结构的PANI/CA复合材料具有良好的电容性能,其比电容可达到410F/g,并且该超级电容器具有较小的内阻和较好的循环稳定性,300次循环后,容量仍维持在342F/g,比电容的保持率为83.4%。 相似文献
972.
Lijun Zhang Qun He Yin Jiang Xun Hu Aimin Yu 《International journal of environmental analytical chemistry》2013,93(11):1250-1261
A new ionic liquid modified silica gel sorbent was prepared from the reaction of active silica gel with N-3-(-3-triethoxysilylepropyl)-3-methylimidazolium chloride ([(TESP)MIm]Cl). This sorbent was exploited as solid phase extractant for separation and preconcentration of metal ions prior to their determination by inductively coupled plasma atomic emission spectrometry (ICP-AES). It was found that it can selectively adsorb Fe(Ш). Identification of the surface modification was performed on the basis of FT-IR. Experimental conditions for effective adsorption of trace Fe(Ш) were optimised using both batch and column procedures. At pH 3, Fe(Ш) could be quantitatively adsorbed and completely eluted by using 2?mL of 0.1?mol?L?1 of HCl. 150?mL of sample solution was adopted as the maximum sample volume and a high enrichment factor of 75 was obtained. Most common coexisting ions did not interfere with the separation and preconcentration of Fe(Ш) at optimal conditions. The maximum static adsorption capacity of the sorbent was 37.0?mg?g?1. The detection limit of the present method was 0.48?µg?L?1, and the relative standard deviation (R. S. D.) was lower than 1.7%. The method was successfully applied to the preconcentration of trace Fe(Ш) in biological and natural water samples with satisfactory results. 相似文献
973.
Qihui Wang Zheng Hu Dandan Li Zhifeng Tu 《International journal of environmental analytical chemistry》2013,93(11):1289-1301
A chelating matrix prepared by immobilising folic acid on silica gel-bound amine phase was used as a new solid-phase extractant. This sorbent has been developed only for preconcentration of trace Pb(II) prior to determination by inductively coupled plasma atomic emission spectrometry (ICP-AES). Experimental conditions were investigated by batch and column procedures. The optimum pH value for the separation of Pb(II) on the new sorbent was 4.0. The adsorbed Pb(II) was quantitatively eluted by 2.0?cm3 of 0.5?mol?dm?3 of HCl. Common coexisting ions did not interfere with the separation and determination of Pb(II). The maximum static adsorption capacity of the sorbent under optimum conditions was found to be 69.23?mg?g?1 for Pb(II). The detection limit of the method defined by International Union of Pure and Applied Chemistry was 0.28?ng?cm?3. The relative standard deviation (RSD) of the method was lower than 2.0% (n?=?8). The developed method has been validated by analysing certified reference materials and successfully applied to the determination of Pb(II) in water samples with satisfactory results. 相似文献
974.
Dr. J. Grant Hill Xiaojun Hu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(11):3620-3628
Benchmark quality geometries and interaction energies for the prereactive halogen‐bonded complexes of dihalogens and ammonia, including hypothetical astatine containing dihalogens, have been produced via explicitly correlated coupled cluster methods. The application of local electron correlation partitioning reveals dispersion, electrostatics and ionic substitutions all contribute significantly to the interaction energy, with a linear relationship between the ionic substitutions and the degree of charge transfer. Potential energy curves for H3N???ClF show that as the relative orientations of the two subunits are manipulated appreciable interactions can be found at considerably angular displaced geometries, signifying lower directionality in halogen bonding than previously supposed. 相似文献
975.
Dr. Weiyi Li Zhishan Su Prof. Dr. Changwei Hu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(1):124-134
The mechanism of the allylation reaction between 4‐chloroacetophenone and pinacol allylboronates catalyzed by ZnEt2 with alcohols was investigated using density functional theory (DFT) at the M05‐2X/6‐311++G(d,p) level. The calculations reveal that the reaction prefers to proceed through a double γ‐addition stepwise reaction mechanism rather than a Lewis acid‐catalyzed concerted one. The intermediate with a four‐coordinated boron center, which is formed through proton transfer from EtOH to the ethyl group of ZnEt2 mediated by the boron center, is the active species and an entrance for the catalytic cycle. The latter is composed of three elementary steps: 1) boron to zinc transmetalation leading to the formation of allylzincate species, 2) electrophilic addition of ketone to allylzincate species, and 3) generation of the final product with recovery of the catalyst. The boron to zinc transmetalation step has the largest energy barrier of 61.0 kJ mol?1 and is predicted to be the rate‐determining step. The calculations indicate that the additive EtOH plays important roles both in lowering the activation free energy for the formation of the four‐coordinated boron active intermediate and in transforming the low catalytic activity ZnEt2 into high activity zinc alkoxide species. The alcohols with a less sterically encumbering R group might be the effective additives. The substituted groups on the allylboronates might primarily affect the boron to zinc transmetalation, and the allylboronates with substituents on the Cγ atom is poor in reactivity. The comparison of the catalytic effect between the zinc compounds investigated suggest that Zn(OEt)2, Zn(OH)2, and ZnF2 exhibit higher catalytic efficiency for the boron to zinc transmetalation due to the activation of the B? Cα bond through orbital interactions between the p orbitals of the EtO, OH, F groups and the empty p orbital of the boron center. 相似文献
976.
Feng Zou Prof. Xianluo Hu Dr. Yongming Sun Dr. Wei Luo Fangfang Xia Long Qie Yan Jiang Prof. Yunhui Huang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(19):6027-6033
Zn2GeO4/N‐doped graphene nanocomposites have been synthesized through a fast microwave‐assisted route on a large scale. The resulting nanohybrids are comprised of Zn2GeO4 nanorods that are well‐embedded in N‐doped graphene sheets by in situ reducing and doping. Importantly, the N‐doped graphene sheets serve as elastic networks to disperse and electrically wire together the Zn2GeO4 nanorods, thereby effectively relieving the volume‐expansion/contraction and aggregation of the nanoparticles during charge and discharge processes. We demonstrate that an electrode that is made of the as‐formed Zn2GeO4/N‐doped graphene nanocomposite exhibits high capacity (1463 mAh g?1 at a current density of 100 mA g?1), good cyclability, and excellent rate capability (531 mAh g?1 at a current density of 3200 mA g?1). Its superior lithium‐storage performance could be related to a synergistic effect of the unique nanostructured hybrid, in which the Zn2GeO4 nanorods are well‐stabilized by the high electronic conduction and flexibility of N‐doped graphene sheets. This work offers an effective strategy for the fabrication of functionalized ternary‐oxide‐based composites as high‐performance electrode materials that involve structural conversion and transformation. 相似文献
977.
Dr. Qingsong Dong Prof. Xiao‐Juan Yang Shida Gong Dr. Qiong Luo Prof. Qian‐Shu Li Prof. Ji‐Hu Su Dr. Yanxia Zhao Prof. Biao Wu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(45):15240-15247
A nickel? nickel‐bonded complex, [{Ni(μ‐L.?)}2] ( 1 ; L=[(2,6‐iPr2C6H3)NC(Me)]2), was synthesized from reduction of the LNiBr2 precursor by sodium metal. Further controllable reduction of 1 with 1.0, 2.0 and 3.0 equiv of Na, respectively, afforded the singly, doubly, and triply reduced compounds [Na(DME)3] ? [{Ni(μ‐L.?)}2] ( 2 ; DME=1,2‐dimethoxyethane), [Na(Et2O)]Na[(L.?)Ni? NiL2?] ( 3 ), and [Na(Et2O)]2Na[L2?Ni? NiL2?] ( 4 ). Here L represents the neutral ligand, L.? denotes its radical monoanion, and L2? is the dianion. All of the four compounds feature a short Ni? Ni bond from 2.2957(6) to 2.4649(8) Å. Interestingly, they display two different structures: the perpendicular ( 1 and 2 ) and the coaxial ( 3 and 4 ) structure, in which the metal? metal bond axis is perpendicular to or collinear with the axes of the α‐diimine ligands, respectively. The electronic structures, Ni? Ni bonding nature, and energetic comparisons of the two structure types were investigated by DFT computations. 相似文献
978.
Composite hydrogels were prepared from pineapple peel cellulose with the combinations of polyethylene glycol (PEG), polyvinyl alcohol (PVA), к-carrageenan (CN), or soluble starch (SH) in 1-allyl-3-methylimidazolium chloride solvent. Impacts of these macromolecules on the texture profile analysis (TPA) parameters, equilibrium swelling ratio (ESR), and sodium salicylate (NaSA) load of the prepared hydrogels were studied. The NaSA release kinetics of the composite hydrogels were also compared. The composite hydrogels exhibited differences in Fourier transform infrared spectroscopy (FTIR), TPA parameters, ESR, NaSA load ratio, and release kinetics. CN addition increased the hardness of the hydrogels, while PEG played an opposite role. SH and PVA could decrease hardness, gumminess, and resilience, and SH could increase the springiness and cohesiveness of the hydrogels. Most of the composite hydrogels exhibited the same basic FTIR features as the simple hydrogel. Freeze-dried composite hydrogels exhibited a markedly higher ESR than the oven-dried ones, and additions of PEG, PVA, CN, and SH showed the same effect. Addition of the PEG and PVA combination could lower the ESR of the hydrogels, whereas additions of the PEG and CN combination or PEG and SH combination could markedly increase the ESR of the hydrogels. Addition of PEG, PVA, CN, and SH respectively could increase the NaSA load ratio of the hydrogels. Oven-drying treatment, additions of the PEG and PVA combination or PEG and CN combination were propitious for extending the NaSA fast-release phase of the hydrogels. 相似文献
979.
980.
Tao Cai Zhen Yang Haijiang Li Hu Yang Aimin Li Rongshi Cheng 《Cellulose (London, England)》2013,20(5):2605-2614
In this present work, a series of hydrolyzed polyacrylamide grafted carboxymethyl cellulose (CMC-g-HPAM) was prepared. The structure and solution properties of CMC-g-HPAM were characterized by FTIR, 1H-NMR, elemental analysis and zeta potential measurements. The graft copolymers were applied as flocculants to remove methylene blue (MB), a cationic dye, from aqueous solutions. In comparison with its precursors, carboxymethyl cellulose (CMC) and polyacrylamide CMC-g-PAM, CMC-g-HPAM exhibited higher removal efficiencies. Furthermore, the flocculation performance of the copolymers was significantly improved with the increase of the hydrolysis degree, and the MB removal efficiency was more than 90 % when the hydrolysis degree of CMC-g-HPAM was higher than 80 %. More importantly, image analysis in combination with fractal theory demonstrated that the graft copolymers could produce notably denser and larger flocs, which was of great significance in practical water treatment. The improved flocculation performance was ascribed to both charge neutralization and bridging effects. 相似文献