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901.
制备了新型纳米B2O3/TiO2吸附材料,并采用扫描电镜(SEM)及红外光谱(IR)对其进行表征,优化了纳米B2O3/TiO2复合材料对试液中痕量银的吸附和解吸条件,建立了纳米B2O3/TiO2分离富集-原子吸收光谱测定痕量银的新方法。当pH 4.3时,在22℃下振荡20 min,Ag+能被该材料快速吸附,其静态饱和吸附容量为11.72 mg/g,吸附在纳米B2O3/TiO2上的Ag+可用0.1 mol/L HNO3-0.05 mol/L硫脲(1∶4)完全洗脱。该方法的检出限为2.01μg/L,线性范围为0.01~4.00 mg/L,相对标准偏差(RSD)为1.8%,加标回收率为95%~105%。方法应用于实际矿渣样品中痕量银的测定,结果满意。 相似文献
902.
903.
利用近共振激光驻波场操纵中性原子实现纳米光栅的沉积是一种新型的研制纳米结构方法,处于激光驻波场中的原子运动速度特性对最终纳米光栅的沉积特性有着重要的影响.利用半经典理论,基于4阶Runge-Kutta算法进行了不同铬原子纵向和横向运动速度条件下纳米光栅结构沉积的仿真研究.研究表明,铬原子纵向速度为最大概率速度960 m/s时,所形成的纳米光栅的半高宽为1.49 nm,对比度为62.1 ∶1,当铬原子的纵向速度为半最大概率速度480 m/s时,纳米光栅的半高宽为5.35 nm,对比度下降为25.6 ∶1.同
关键词:
原子光刻
纳米计量
激光驻波场
纳米光栅结构 相似文献
904.
Ashfaq Khan Zengbo WangMohammad A. Sheikh David J. WhiteheadLin Li 《Applied Surface Science》2011,258(2):774-779
Direct laser surface micro/nanopatterning by using Contact Particle Lens Array (CPLA) has been widely utilized. The method involves laser scanning of a monolayer of transparent particles arranged on the substrate to be patterned. Despite the different techniques available for CPLA deposition; the particles monolayer can only be formed on hydrophilic surfaces, which restrict the range of substrates that could be patterned by this method. In this study, a technique for patterning of hydrophobic surfaces by using CPLA has been proposed. In the proposed technique, monolayer of CPLA is formed on a hydrophilic substrate and then transported to a hydrophobic substrate by using a flexible sticky plastic. The transported CPLA is then scanned by a laser for patterning the hydrophobic substrate. The plastic pre-selected for this work was transparent to the laser. Experimental investigations were carried out to generate bumps and bowl shaped patterns using transported particles. Features smaller than the diffraction limit have been generated. The optical near field and associated temperatures around the particles were numerically simulated with a coupled electromagnetic and thermal modelling technique. 相似文献
905.
Abdelftah M. Badawi Nadia I. Zakhary Gilane M. Sabry Mohamed R. Mohamed Ahmed M. Mousa 《Journal of Dispersion Science and Technology》2013,34(9):1303-1309
The in vitro anticancer activity of copper cetyl trimethyl ammonium bromide (Cu-CTAB)-loaded cyclodextrin nanoparticles on Ehrlich ascites carcinoma (EAC), colon cancer cells (HCT 116), liver cancer cells (HepG-2), breast cancer cells (MCF-7), and cervix cancer cells (Hela) was investigated using MTT due assay. Cyclodextrin nanoparticles loaded with Cu-CTAB exerted in vitro anticancer activity against the previous human cancer cell lines comparable to the activity of free non-entrapped in nanoparticles macro-particle Cu-CTAB. The nano analog was synthesized by physical loading using grinding with ball mill. The ratio between Cu-CTAB and cyclodextrin oligosaccharide was 1 Cu-CTAB: 3 cyclodextrin. The particle size of the nano derivative was determined using the transmitted electron microscope (TEM). 相似文献
906.
The batch removal of Cr(VI) ions from aqueous solution using binary composite microspheres of chitosan and nanoparticles of iron oxide under different conditions has been investigated in this study. The influences of initial chromium concentration, contact time, pH, temperature, and solid-liquid ratio have been reported. The adsorption data was fitted well in the Langmuir and Freundlich models and various static parameters were calculated. The mechanism of adsorption was studied by Fourier Transform Infrared spectroscopy (FTIR). 相似文献
907.
Meenachi S Kandasamy S 《International journal of environmental analytical chemistry》2013,93(13):1286-1297
ABSTRACTThe present study aimed that non-toxic, less expensive, easily available, safer to environment and previously unreported Eclipta prostrata leaf extract is used for the green synthesis of iron oxide nano particles. The iron oxide nanoparticles (NPs) were characterised by UV–visible, Fourier Transform Infrared Spectroscopy (FTIR), scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDX), X-ray diffraction (XRD) and transmission electron microscopy (TEM). Tannery effluents treated by photodegradation process and the removal efficiency of chemical oxygen demand (COD), biological oxygen demand (BOD) and sulphide were analysed. The maximum removal efficiency correlated with operating parameters was explained using response surface methodology with Boxmen Beckmen design. 相似文献
908.
Star homopolymers of some vinyl monomers such as methyl methacrylate, n‐butyl methacrylate and styrene (MMA, nBMA, St.) were prepared by using a N,N,N′N′‐tetramethylethylenediamine ligand/CuBr catalytic system via atom transfer radical polymerization (ATRP). A three armed benzene based core was successfully used as initiator. Low polydispersities and regular molecular weight values were obtained in most cases, especially at low conversions. MMA and BMA showed comparable behavior where controlled and true ATRP was observed even at high conversions. However, styrene monomer recorded irregular high polydispersities at high conversions in spite of the relatively low molecular weight values. Some block copolymers were obtained using MMA homopolymer as macroinitiator with the same strategy of ATRP. 1H‐NMR confirmed the structures of the resulting polymers. Transmission electron microscopy (TEM) proved the nano‐structure of the star polymers. The thermal behavior of the MMA star homo and copolymers was studied. The effect of the star shape on thermal behavior was very clear with respect to the linear ones. 相似文献
909.
A modified nano‐hydrotalcite was used as inorganic flame‐retardant fillers for poly(ethylene terephthalate) (PET) polymers. A flame‐retardant compound was obtained from layered hydrotalcite (LDH) dispersed in brominated polystyrene (PBS) solution and then solvent evaporation from the dissolved PBS samples. The compound of PBS/LDH was characterized by X‐ray diffraction (XRD), transmission electron microscopy (TEM) and thermogravimetric analysis (TGA) and was found to have high aspect ratio LDH dispersed in the PBS matrix. Flame‐retardant PET composite was prepared by melt‐compounding the flame‐retardant compound of PBS/LDH and PET. Improvement in the fire retardancy of the nano‐flame‐retardant PET composite obtained was found by measuring the oxygen index. The nanostructure of flame‐retardant PET composite was chirecterized by scanning electron microscopy (SEM) of flame‐retardant PET composite. The mechanical properties of the flame‐retardant PET nano‐composite were also characterized. 相似文献
910.
Natural rubber composites with alumina of different particle sizes (28 nm nano particles, 200 nm active particles and > 1000 nm raw alumina) were prepared by the usual rubber processing technique. Epoxidized natural rubber (ENR) was used in the composites as compatibilizer. Cure characteristics and mechanical properties of all composites were analyzed. The values of minimum rheometric torque (ML), maximum rheometric torque (MH) and torque difference (MH – ML) increased. Maximum enhancement was observed for the nano-filled composites. It endorses the view that nano alumina reveals highest interaction with natural rubber in presence of ENR. Scorch time and optimum cure time values for nano-composites were highest among all types of composites. Vulcanization reaction for the sulfur curing system of the composites was found to follow first order rate kinetics. Specific rate constant decreased with decreasing particle size in composites. Crosslink densities of composite-vulcanizates showed increasing trend with decreasing particle size of alumina. Mechanical properties of the composite vulcanizates increased with decreasing particle size of alumina - nano composites exhibiting much higher mechanical strength. Results of oxidative resistance reveal that particle size of alumina in composite vulcanizates has a significant impact on aging behavior. 相似文献