共查询到20条相似文献,搜索用时 15 毫秒
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Helmi Keskinen Sami Romakkaniemi Antti Jaatinen Pasi Miettinen Erkka Saukko Joutsensaari Jorma 《Aerosol science and technology》2013,47(12):1441-1447
The first wetting layer on solid nanoparticles has direct implications on the roles these particles play in industrial processes and technological applications as well as in the atmosphere. We present a technique for online measurements of the adsorption of the first few water layers onto insoluble aerosol nanoparticles. Atomized fumed silica nanoparticles were dispersed from aqueous suspension and their hygroscopic growth factors (HGF) and number of the adsorbed water layers at subsaturated conditions were measured using a nanometer hygroscopic tandem differential mobility analyzer (HTDMA). Particle morphology was characterized by electron microscopy and particle density was determined by mobility analysis. The HGFs of the size-selected particles at mobility diameters from 10 to 50 nm at 90% relative humidity (RH) varied from 1.05 to 1.24, corresponding to 2–6 layers of adsorbed water. The morphology of the generated fumed silica nanoparticles varied from spheres at 8–10 nm to agglomerates at larger diameters with effective density from 1.7 to 0.8 g/cm3 and fractal dimension of 2.6. The smallest spheres and agglomerates had the highest HGFs. The smallest particles with diameters of 8 and 10 nm adsorbed two to three water layers in subsaturated conditions, which agreed well with the Frenkel, Halsey, and Hill (FHH) isotherm fitting. In comparison to the small spheres or large agglomerates, the compact agglomerate structure containing a few primary particles increased the number of adsorbed water layers by a factor of ~1.5. This was probably caused by the capillary effect on the small cavities between the primary particles in the agglomerate. 相似文献
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Fumed silica is a synthetic amorphous silicon dioxide produced by burning silicon tetrachloride in an oxygen-hydrogen flame. Surface areas range from 50–400 m2/g. Using particle sizing techniques, fumed silica shows micron sized particles leading to surface areas markedly lower than expected. Fumed silica appears as a fluffy solid with bulk densities down to 0.03 g/cm3, being invariant over the wide range of surface areas. Attempts to relate the variation of the surface area directly to the performance of fumed silica in technical applications, such as its thickening efficiency in fluids, mainly fail and remain ambiguous. 相似文献
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Toshiki Kono Yanming Hu Toshio Masuda Katsuchisa Tanaka Rodney D. Priestley Benny D. Freeman 《Polymer Bulletin》2007,58(5-6):995-1003
Summary The gas permeability of three substituted polyacetylenes, poly(1-chloro-2-phenylacetylene) (PClPA), poly[1-phenyl-2-(4-trimethylsilyl)phenylacetylene]
(PTMSDPA), and poly[1-(trimethylsilyl)-1-propyne] (PTMSP), increased systematically with increasing content of nonporous fumed
silica (FS) nanoparticles. For instance, the oxygen permeability coefficient (PO2) of PClPA containing 30 wt % FS was 86 barrers, which was 10 times higher than that of the unfilled polymer (PO2=8.6 barrers). The extent of permeability increase with the addition of FS was smaller when the permeability of the original
polymer was higher. The order of the permeability increase in FS-filled polymers was as follows: PClPA > PTMSDPA > PTMSP.
The addition of FS resulted in the decrease of O2/N2 permselectivity of these polymers. The H2/CH4 permselectivity largely decreased with increasing FS content in PClPA, while it hardly changed with FS loading in PTMSP.
The gas solubility of PClPA was practically independent of FS content, and the increase in gas permeability in filled PClPA
resulted from an increase in diffusivity with the addition of FS. 相似文献
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Raja Wusirika 《Journal of the American Ceramic Society》1990,73(10):2926-2929
The reaction between fumed silica and ammonia has been studied between 600° and 1200°C. Up to 24 wt% nitrogen can be introduced into vitreous silica by adjusting the partial pressure of ammonia, temperature, and reaction time. The experiments show that the amount of nitrogen incorporated into silica has a linear dependence on the partial pressure of ammonia and a square root dependence on the reaction time. The activation energy for the reaction was found to be 76.0 kJ/mol. The nitrided powders as well as several hotpressed samples were crystallized at 1550° to 1650°C. Silica glasses containing 0 to 1 wt% nitrogen crystallize to cristobalite. Glasses containing 2 to 10 wt% nitrogen are stable against devitrification in nitrogen, even at 1650°C. Glasses with 12 to 28 wt% nitrogen crystallize to fine-grained Si2 N2 O with residual glass. 相似文献
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JustinL. Sabourin RichardA. Yetter BlaineW. Asay JosephM. Lloyd VictorE. Sanders GrantA. Risha StevenF. Son 《Propellants, Explosives, Pyrotechnics》2009,34(5):385-393
The heterogeneous interaction between nitromethane (NM), particles of nanoscale aluminum (38 and 80 nm diameter), and fumed silica is examined in terms of the deflagration and detonation characteristics. Burning rates are quantified as functions of pressure using an optical pressure vessel up to 14.2 MPa, while detonation structure is characterized in terms of failure diameter. Nitromethane is gelled using fumed silica (CAB‐O‐SIL®), as well as by the nanoaluminum particles themselves. Use of nanoaluminum particles with fumed silica slightly increases burning rates compared to the use of larger diameter Al particles; however distinct increases in burning rates are found when CAB‐O‐SIL is removed and replaced with more energetic aluminum nanoparticles, whose high surface area allows them to also act as the gellant. Mixtures including fumed silica yield a reduced burning rate pressure exponent compared to neat NM, while mixtures of aluminum particles alone show a significant increase. Failure diameters of mixture detonations are found to vary significantly as a function of 38 nm aluminum particle loading, reducing more than 50% from that of neat nitromethane with 12.5% (by mass) aluminum loading. Failure diameter results indicate a relative minimum with respect to particle separation (% loading) which is not observed in other heterogeneous mixtures. 相似文献
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