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121.
Air plasma treatment, coupled to a masking technique, was used to promote micropatterned cell adhesion onto a cell-adhesion-resistant alginate coated surface. L-929 mouse fibroblasts were successfully confined into 50 m diameter cell-adhesive areas patterned inside a cell-resistant layer. The plasma treatment performed, albeit very mild, destroys the molecular architecture of the hydrophilic polysaccharide coating, leading to an enhancement of protein adsorption and hence of cell-adhesion. Both the cell-adhesion-resistant and the cell-adhesive regions are hydrophilic, yet they show a completely different behavior towards cells. Thus, they are a very interesting subject in the study of interfacial interactions in aqueous media, and, in particular, on the mechanisms of bio-adhesion at hydrophilic surfaces.  相似文献   
122.
A facile and low-cost superhydrophobic nanocomposite coating on paper surface was fabricated through one-step simply spraying dispersion, using hydrophobic silica nanoparticles as a filter (SiNPs) and polyvinylidene fluoride (PVDF) as a film-forming material. Hydrophobic SiNPs were fabricated via co-hydropholysis and condensation of TEOS and long-chain alkyl silane based on a simple sol-gel process, and the surface chemical structure of SiNPs was characterized by Fourier transform infrared (FTIR) spectra. The wettability and morphology of the coating surface were measured by contact angle (CA) measurement and scanning electron microscope, respectively. The influence of the mass ratio of hydrophobic SiNPs to PVDF (M(SiNPs:PVDF)) on the superhydrophobicity of paper surface was studied. The results showed that when M(SiNPs:PVDF) was 3:1, the water CA was 156.0 ± 1.0° for the nanocomposite coating with micro/nano-hierarchical structure on paper surface. Further, such superhydrophobic nanocomposite coatings on paper surface showed little adhesive property with water. In addition, the prepared superhydrophobic nanocomposite coating could be applied in other substrates, such as wood, aluminum sheet, stainless steel, polytetrafluoroethylene (PTFE), etc.  相似文献   
123.
In the membrane distillation process only gaseous phase can exist in the membrane pores. The resistance to wettability of capillary polypropylene membranes has been investigated in this work. The SEM-EDS investigations revealed that the pores located up to 100 μm from the membrane surface were filled by the feed during the production of demineralized water over a period of 4500 h. However, the pores located inside the membrane wall were still dry and no feed leakage was observed. Both scaling and polypropylene degradation were indicated as the major reason for partial membrane wettability. The SEM-EDS, XRD and FTIR methods were used for investigations of polypropylene degradation, and material cracking and the presence of hydroxyl and carbonyl groups on the membrane surface has been identified. The membranes irradiated by UV light or stored up to 9 years in air were used to evaluate the membrane wetting caused by the products of polymer oxidation. The membrane samples were soaked in either water or a concentrated solution of NaCl at temperature of 343 K, and their wettability was evaluated on the basis of their variations in the air permeability. It was found that the products of polypropylene oxidation significantly accelerated the degree of wettability during the first 30 days of investigations, but after 60 days the results were similar. The soaked membrane samples wetted faster in NaCl solutions than those soaked in distilled water, which came as a result of the chemical reactions of salt with the hydroxyl and carbonyl groups found on the polypropylene surface.  相似文献   
124.
Summary: The impact of a droplet on a solid surface, pre‐patterned with a barrier, was studied using a diffuse interface model. The effect of the wettability of the barrier material and the width of the barrier on droplet spreading was investigated. The results show that depending on the barrier wettability and width, the flow of the spreading droplet can be controlled and that the droplet may or may not overflow the barrier.

Droplet shapes with the corresponding velocity field for different barrier contact angles at ± = 1.5.  相似文献   

125.
Janca  J.  Stahel  P.  Buchta  J.  Subedi  D.  Krcma  F.  Pryckova  J. 《Plasmas and Polymers》2001,6(1-2):15-26
Polyester tire cord surfaces have been modified by plasma at low temperature and atmospheric pressure. The surface treatment has been executed by various nonequilibrium discharges, namely by barrier discharge, atmospheric pressure glow discharge and gliding arc. The polymeric multicord sewing threads treated by this procedure have been used in the same form as in industry, i.e., with the protecting oil films on their surface. The surface properties have been investigated by electron spin resonance spectroscopy and by measuring their contact angle with various liquids; partially the zeta potential measurements have been used, too. Further tests have been done at an industrial testing impregnation line using the common technology and conditions, on both plasma treated and untreated fibers. Finally, the standard H-tests and peel-tests have been used to characterize the fiber adhesion to usual testing rubbers.  相似文献   
126.
127.
This article demonstrates a water‐lubrication system using high‐density hydrophilic polymer brushes consisting of 2,3‐dehydroxypropyl methacrylate (DHMA), vinyl alcohol, oligo(ethylene glycol)methyl ether methacrylate, 2‐(methacryloyloxy)ethyltrimethylammonium chloride (MTAC), 3‐sulfopropyl methacrylate potassium salt (SPMK), and 2‐methacryloyloxyethyl phosphorylcholine (MPC) prepared by surface‐initiated controlled radical polymerization. Macroscopic frictional properties of brush surfaces were characterized by sliding a glass ball probe in water using a ball‐on‐plate type tribotester under the load of 0.1–0.49 N at the sliding velocity of 10?5–10?1 m s?1 at 298 K. A poly(DHMA) brush showed a relatively larger friction coefficient in water, whereas the polyelectrolyte brushes, such as poly(SPMK) and poly(MPC), revealed significantly low friction coefficients below 0.02 in water and in humid air conditions. A drastic reduction in the friction coefficient of polyelectrolyte brushes in aqueous solution was observed at around 10?3–10?2 m s?1 owing to the hydrodynamic lubrication effect, however, an increase in salt concentration in the aqueous solution led to the increase in the friction coefficients of poly(MTAC) and poly(SPMK) brushes. The poly(SPMK) brush showed a stable and low friction coefficient in water even after sliding over 450 friction cycles, indicating a good wear resistance of the brush film. © 2010 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 10: 208–216; 2010: Published online in Wiley InterScience ( www.interscience.wiley.com ) DOI 10.1002/tcr.201000001  相似文献   
128.
纳米聚硅材料在油藏注水井中降压增注的室内研究   总被引:1,自引:0,他引:1  
应用聚硅纳米材料在油田注水井中降压增注的室内实验表明,纳米聚硅材料能够改变岩石润湿性、提高水相相对渗透率,一同时说明聚硅材料易吸附于岩石表面能改变界面性质,其强憎水特性能够驱替吸附在孔隙内表面的水膜,扩大孔径.所以纳米聚硅材料能降低注水压力,提高注水量,具有较好的经济效益.  相似文献   
129.
The bioinspired leaf‐like super‐hydrophobic surfaces on aluminum alloy were fabricated by means of a facile method using anodic oxidation. The surface morphologies, compositions, and wettability were investigated with SEM, XPS, and contact angle measurement, respectively. The SEM showed hierarchical microstructures and nanostructures, the static contact angle was about 167.7 ± 1.2°, and sliding angle was 5°. The super‐hydrophobic phenomenon of the prepared surface was analyzed with Cassie theory, and it is found that only about 3% of the water surface is contacted with the metal substrate and the remaining 97% is contacted with the air cushion. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   
130.
This paper begins with an extensive review of the formation of gas bubbles, with a particular focus on the dynamics of triple lines, in a pure liquid and progresses into an experimental study of bubble formation on a micrometer-sized nozzle immersed in a quiescent pool of aqueous gold nanofluid. Unlike previous studies of triple line dynamics in a nanofluid under evaporation or boiling conditions, which are mainly caused by the solid surface modification due to particle sedimentation, this work focuses on the roles of nanoparticles suspended in the liquid phase. The experiments are conducted under a wide range of flow rates and nanoparticle concentrations, and many interesting phenomena are revealed. It is observed that nanofluids prevent the spreading of the triple line during bubble formation, i.e. the triple line is pinned somewhere around the middle of the tube wall during the rapid bubble formation stage whereas it spreads to the outer edge of the tube for pure water. A unique ‘stick-slip’ movement of the triple line is also observed for bubbles forming in nanofluids. At a given bubble volume, the radius of the contact line is found to be smaller for higher particle concentrations, but a reverse trend is found for the dynamic bubble contact angle. With the increase of particle concentration, the bubble frequency is raised and the bubble departure volume is decreased. The bubble shape is found to be in a good agreement with the prediction from Young-Laplace equation for given flow rates. The influence of nanoparticles on other detailed characteristics related to bubble growth inside, including the variation of bubble volume expansion rate, the radius of the curvature at the apex, the bubble height and bubble volume, is revealed. It is suggested that the variation of surface tensions and the resultant force balance at the triple line might be responsible for the modified dynamics of the triple line.  相似文献   
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