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Cypsela dormancy in Scotch thistle (Onopordum acanthium) may be affected by the presence of chemical inhibitors. To investigate this phenomenon, a leachate from O. acanthium cypselas was tested for its ability to inhibit germination of the cypselas from which it was derived (i.e., autoinhibition). Leachates varied in their degree of autoinhibition, depending on the cypsela population from which they were prepared. Overall, removal of leachate from a group of O. acanthium cypselas increased their germinability. Using lettuce (Lactuca sativa) cypselas as an indicator species, bioactivity-guided fractionation was used to isolate a water-soluble, para-substituted benzamide from O. acanthium cypselas, which caused germination inhibition. Various chromatographic, spectroscopic, and spectrometric techniques were applied to the characterization of the bioactive compound.  相似文献   
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We have employed scanning force microscopy (SFM) and nanoindentation analysis to track the evolution of tribologically generated antiwear films derived from zinc dialkyldithiophosphate (ZDDP) as a function of rubbing time. The SFM images reveal that film morphology evolves with time through a growth mechanism consisting of three stages. In the first stage nucleation on active sites at the steel surface leads to the growth of distinct segregated islands. In the second stage the islands coalesce causing the film to spread over a larger fraction of the surface. In the final stage continuous rubbing induces the large islands to divide into smaller, densely packed structures. In contrast to the observed morphological changes, rubbing time does not strongly influence the nanomechanical properties of the films. This highlights the importance of film morphology in determining the effectiveness of ZDDP antiwear films. We also observe large variation in both the morphology and nanomechanical properties that are likely due to the heterogeneity in contact pressure at the pin-sample interface of the wear rig.  相似文献   
3.
The incorporation of carbon materials in micro‐ and nanoscale devices is being widely investigated due to the promise of enhanced functionality. Challenges in the positioning and addressability of carbon nanotubes provide the motivation for the development of new processes to produce nanoscale carbon materials. Here, the fabrication of conducting, nanometer‐sized carbon structures using a combination of electron beam lithography (EBL) and carbonisation is reported. EBL is used to directly write predefined nanometer‐sized patterns in a thin layer of negative resist in controllable locations. Careful heat treatment results in carbon nanostructures with the size, shape, and location originally defined by EBL. The pyrolysis process results in significant shrinkage of the structures in the vertical direction and minimal loss in the horizontal direction. Characterization of the carbonized material indicates a structure consisting of both amorphous and graphitized carbon with low levels of oxygen. The resistivity of the material is similar to other disordered carbon materials and the resistivity is maintained from the bulk to the nanoscale. This is demonstrated by fabricating a nanoscale structure with predictable resistance. The ability to fabricate these conductive structures with known dimensions and in predefined locations can be exploited for a number of applications. Their use as nanoband electrodes is also demonstrated.  相似文献   
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