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The structure of (NH4)2B10H10 (1) was determined through powder XRD analysis. The thermal decomposition of 1 and (NH4)2B12H12 (2) was examined between 20 and 1000 °C using STMBMS methods. Between 200 and 400 °C a mixture of NH3 and H2 evolves from both compounds; above 400 °C only H2 evolves. The dihydrogen bonding interaction in 1 is much stronger than that in 2. The stronger dihydrogen bond in 1 resulted in a significant reduction by up to 60 °C, but with a corresponding 25% decrease in the yield of H2 in the lower temperature region and a doubling of the yield of NH3. The decomposition of 1 follows a lower temperature exothermic reaction pathway that yields substantially more NH3 than the higher temperature endothermic pathway of 2. Heating of 1 at 250 °C resulted in partial conversion of B10H102− to B12H122−. Both 1 and 2 form an insoluble polymeric material after decomposition. The elements of the reaction network that control the release of H2 from the B10H102− can be altered by conducting the experiment under conditions in which pressures of NH3 and H2 are either near, or away from, their equilibrium values.  相似文献   
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Due to their unusual electronic and vibrational properties, single walled carbon nanotubes (SWCNTs) with sub-nanometer diameters d ∼ 0.5–0.9 nm have recently gained interest in the carbon community. Using UV–Vis–NIR spectroscopy and ultra-centrifugation, we have conducted a detailed study of the π plasmon energy (present at∼5–7 eV) in sub-nm SWCNTs as a function of the size of the bundle. We find that the energy of the π plasmon peak E varies with the bundle diameter Dh as E = (-0.023 eV)ln(Dh/do) + 5.37 eV, where do = 0.5 nm and corresponds to the smallest tube diameter.1 This is compared with the same data for HiPCo and Carbolex SWCNTs of larger diameter (1–1.4 nm) confirming a clear dependence of E on the bundle size, which is present in addition to the previously reported dependence of E on SWCNT diameter d.  相似文献   
4.

Coverage of the bounded region gets importance in Wireless Sensor Network (WSN). Area coverage is based on effective surface coverage with a minimum number of sensor nodes. Most of the researchers contemplate the coverage region of interest as a square and manifest the radio ranges as a circle. The area of a circle is much higher than the area of a square because of the perimeter. To utilize the advantage of the circle, the coverage region of interest is presumed as a circle for sensor node deployment. This paper proposes a novel coverage improved disc shape deployment strategy. Comparative analysis has been observed between circle and square regions of interest based on the cumulative number of sensor nodes required to cover the entire region. A new strategy named as disc shape deployment strategy is also proposed. Traditional hexagon and strip-based deployment strategies are compared with the disc shape deployment strategy. The simulation result shows that the circle shape coverage region of interest extremely reduces the required number of sensor nodes. The proposed deployment strategy provides desirable coverage, and it requires few more sensor nodes than hexagon shape deployment strategy.

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The coal blend quality and process control of coke making technologies is an important lever to produce quality coke with optimal cost. Apart from impacting cost, this improves the CO2 footprint. This is facilitated by proper selection of coke making technologies and coal/coal blend. Each technology has its own advantage and limitation based on its design criteria. Recently, Tata Steel introduced Asia largest single location 1.6 mtpa of heat recovery coke plant for the first time. This paper briefly described the operational philosophy evolved in heat recovery coke plant to produce desired quality coke at comparatively lower cost through operational excellence. The reduction of imported prime hard coking coal in coal blend up to 30% without affecting coke quality adversly and understanding the operational processes and finally mastering heat recovery coke making technology was also part of this paper.  相似文献   
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The aim of the investigation is to develop solid lipid nanoparticles (SLN) and nano-structured lipid carrier (NLC) as carriers for topical delivery of nitrendipine (NDP). NDP-loaded SLN and NLC were prepared by hot homogenization technique followed by sonication, and they were characterized for particle size, zeta potential, entrapment efficiency, stability, and in vitro release profiles. Also the percutaneous permeation of NDPSLN A, NDPSLN B, and NDPNLC were investigated in abdominal rat skin using modified Franz diffusion cells. The steady state flux, permeation coefficient, and lag time of NDP were estimated over 24 h and compared with that of control (NDP solution). The particle size was analyzed by photon correlation spectroscopy (PCS) using Malvern zeta sizer, which shows that the NDPSLN A, NDPSLN B, and NDPNLC were in the range of 124-300 nm during 90 days of storage at room temperature. For all the tested formulations (NDPSLN A, NDPSLN B, and NDPNLC), the entrapment efficiency was higher than 75% after 90 days of storage. The cumulative percentage of drug release at 24 h was found to be 26.21, 30.81, and 37.52 for NDPSLN A, NDPSLN B, and NDPNLC, respectively. The results obtained from in vitro release profiles also indicated the use of these lipid nanoparticles as modified release formulations for lipophilic drug over a period of 24 h. The data obtained from in vitro release from NDPSLN A, NDPSLN B, and NDPNLC were fitted to various kinetic models. High correlation was obtained in Higuchi and Weibull model. The release pattern of drug is analyzed and found to follow Weibull and Higuchi equations. The permeation profiles were obtained for all formulations: NDPSLN A, NDPSLN B, and NDPNLC. Of all the three formulations, NDPNLC provided the greatest enhancement for NDP flux (21.485 +/- 2.82 microg/h/cm(2)), which was fourfold over control (4.881 +/- 0.96 microg/h/cm(2)). The flux obtained with NDPSLN B (16.983 +/- 2.91 microg/h/cm(2)) and NDPNLC (21.485 +/- 2.82 microg/h/cm(2)) meets the required flux (16.85 microg/h/cm(2)).  相似文献   
8.
The aim of the investigation is to develop solid lipid nanoparticles (SLN) and nano-structured lipid carrier (NLC) as carriers for topical delivery of nitrendipine (NDP). NDP-loaded SLN and NLC were prepared by hot homogenization technique followed by sonication, and they were characterized for particle size, zeta potential, entrapment efficiency, stability, and in vitro release profiles. Also the percutaneous permeation of NDPSLN A, NDPSLN B, and NDPNLC were investigated in abdominal rat skin using modified Franz diffusion cells. The steady state flux, permeation coefficient, and lag time of NDP were estimated over 24 h and compared with that of control (NDP solution). The particle size was analyzed by photon correlation spectroscopy (PCS) using Malvern zeta sizer, which shows that the NDPSLN A, NDPSLN B, and NDPNLC were in the range of 124–300 nm during 90 days of storage at room temperature. For all the tested formulations (NDPSLN A, NDPSLN B, and NDPNLC), the entrapment efficiency was higher than 75% after 90 days of storage. The cumulative percentage of drug release at 24 h was found to be 26.21, 30.81, and 37.52 for NDPSLN A, NDPSLN B, and NDPNLC, respectively. The results obtained from in vitro release profiles also indicated the use of these lipid nanoparticles as modified release formulations for lipophilic drug over a period of 24 h. The data obtained from in vitro release from NDPSLN A, NDPSLN B, and NDPNLC were fitted to various kinetic models. High correlation was obtained in Higuchi and Weibull model. The release pattern of drug is analyzed and found to follow Weibull and Higuchi equations. The permeation profiles were obtained for all formulations: NDPSLN A, NDPSLN B, and NDPNLC. Of all the three formulations, NDPNLC provided the greatest enhancement for NDP flux (21.485 ± 2.82 μg/h/cm2), which was fourfold over control (4.881 ± 0.96 μg/h/cm2). The flux obtained with NDPSLN B (16.983 ± 2.91 μg/h/cm2) and NDPNLC (21.485 ± 2.82 μg/h/cm2) meets the required flux (16.85 μg/h/cm2).  相似文献   
9.
For a practical realization of graphene‐based logic devices, the opening of a band gap in graphene is crucial and has proven challenging. To this end, several synthesis techniques, including unzipping of carbon nanotubes, chemical vapor deposition, and other bottom‐up fabrication techniques have been pursued for the bulk production of graphene nanoribbons (GNRs) and graphene quantum dots (GQDs). However, only limited progress has been made towards a fundamental understanding of the origin of strong photoluminescence (PL) in GQDs. Here, it is experimentally shown that the PL is independent of the functionalization scheme of the GQDs. Following a series of annealing experiments designed to passivate the free edges, the PL in GQDs originates from edge‐states, and an edge‐passivation subsequent to synthesis quenches the PL. The results of PL studies of GNRs and carbon nano‐onions are shown to be consistent with PL being generated at the edge sites of GQDs.  相似文献   
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