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Web-based tools developed in the last couple of years offer unique opportunities to effectively support scientists in their effort to collaborate. Communication among environmental researchers often involves not only work with geographical (spatial), but also with temporal data and information. Literature still provides limited documentation when it comes to user requirements for effective geo-collaborative work with spatio-temporal data. To start filling this gap, our study adopted a User-Centered Design approach and first explored the user requirements of environmental researchers working on distributed research projects for collaborative dissemination, exchange and work with spatio-temporal data. Our results show that system design will be mainly influenced by the nature and type of data users work with. From the end-users' perspective, optimal conversion of huge files of spatio-temporal data for further dissemination, accuracy of conversion, organization of content and security have a key role for effective geo-collaboration.  相似文献   
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New microfiltration and ultrafiltration membranes were obtained using acrylonitrile‐vinyl acetate copolymers in mixture with poly(vinyl alcohol) (PVA). Thus, a blend polymer solution was prepared in dimethylsulfoxide (DMSO) and used to obtain bicomponent polymer membranes by phase inversion. The rheological behavior of the DMSO polymer solutions was, mostly, dilatant at low shear gradients and pseudo plastic with quasi Newtonian tendency at higher gradients. Membranes were characterized by Fourier transform infrared spectrometry (FTIR), optical microscopy, atomic force microscopy, thermal gravimetric analysis‐differential thermal gravimetry, and pure water flux (PWF). FTIR spectra displayed the characteristic bands for acrylonitrile, vinyl acetate, and PVA. The morphology and the porosity can be tailored by the preparation conditions. PVA allows controlling the size of the pores and enables, in principle, to use the resulted membranes as supports for enzyme immobilization. PVA content influences the thermal stability. PWF values depend on the copolymer, on the content in PVA, but also on the coagulation bath composition. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41013.  相似文献   
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Polypropylene electrets 20-μm thick obtained in a corona discharge were studied. After the electrets were charged, they were put into a vacuum chamber at various pressures and the electret surface potential was measured over a 1-h period. A desorption from the electrets is suggested to explain the results obtained.  相似文献   
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The preparation of activated carbons from bean pods waste by chemical (K(2)CO(3)) and physical (water vapor) activation was investigated. The carbon prepared by chemical activation presented a more developed porous structure (surface area 1580 m(2) g(-1) and pore volume 0.809 cm(3) g(-1)) than the one obtained by water vapor activation (258 m(2) g(-1) and 0.206 cm(3) g(-1)). These carbons were explored as adsorbents for the adsorption of naphthalene from water solutions at low concentration and room temperature and their properties are compared with those of commercial activated carbons. Naphthalene adsorption on the carbons obtained from agricultural waste was stronger than that of carbon adsorbents reported in the literature. This seems to be due to the presence of large amounts of basic groups on the bean-pod-based carbons. The adsorption capacity evaluated from Freundlich equation was found to depend on both the textural and chemical properties of the carbons. Naphthalene uptake on biomass-derived carbons was 300 and 85 mg g(-1) for the carbon prepared by chemical and physical activation, respectively. Moreover, when the uptake is normalized per unit area of adsorbent, the least porous carbon displays enhanced naphthalene removal. The results suggest an important role of the carbon composition including mineral matter in naphthalene retention. This issue remains under investigation.  相似文献   
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Electret stability of poly(L ‐lactide) (PLA) films, gamma‐irradiated up to 100 kGy has been investigated by measuring the surface potential during the storage period. PLA samples—40‐μm thick films—were prepared by the casting method and then irradiated in a 60Co radiation facility at a dose rate of 0.25 kGy/h. The structural changes during the irradiation were estimated by viscometric, differential scanning calorimetry and scanning electron microscope measurements. Random chain scission and appearance of end radicals are the most probable results of the irradiation process. After irradiation, the samples were charged in a corona discharge system and surface potential was measured by the method of the vibrating electrode with compensation. The values of the surface potential of the irradiated samples were higher in comparison with the non‐irradiated samples. This effect could be related to the degradation of the macromolecules and changes in the crystal state of PLA during the irradiation. Both of the mentioned factors lead to structural defects that increase the number of discrete trapping levels. The effect of low pressure on the surface potential drop was also investigated. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   
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