The use of the linear Fresnel lens as a seasonally adjusted or one-axis tracked solar concentrator is investigated. Ray tracing techniques are used to show that this type of concentrator is very good in the period of time within 1 hr of solar noon. However, increased refraction due to increased incident angles of the solar rays causes a sharp drop-off in energy delivered to the absorber at other hours of the day. Daily collection efficiencies are typically 50 per cent at concentration ratios of near 5. Effects of absorber width, distance from the lens to the absorber and alignment accuracy are considered in detail. Energy collected over a year's time is calculated assuming cloudless skies. Qualitative experimental results are presented that confirm the analytical results. 相似文献
Diurnal patterns for dissolved gaseous mercury (DGM) concentration, mercury flux, several water variables (pH, oxidation reduction potential (ORP), water temperature), and meteorological variables (wind speed, air temperature, % relative humidity, solar radiation) were measured in two lakes with contrasting dissolved organic carbon (DOC) concentrations in Kejimkujik Park, Nova Scotia. A continuous analysis system made it possible to measure quick changes in DGM over time. Consistently higher DGM concentrations were found in the high DOC lake as compared to the low DOC lake. An examination of current mercury flux models using this quantitative data indicated some good correlations between the date and predicted flux (r ranging from 0.27 to 0.83) but generally poor fit (standard deviation of residuals ranging from 0.97 to 3.39). Cross-correlation analysis indicated that DGM dynamics changed in response to solar radiation with lag-times of 65 and 90 min. This relationship with solar radiation was used to develop new predictive models of DGM and mercury flux dynamics for each lake. We suggest that a generalized approach using time-shifted solar radiation date to predict DGM can be incorporated into existing mercury flux models. It is clear from the work presented that DOC and wind speed may also play important roles in DGM and mercury flux dynamics, and these roles have not been adequately accounted for in current predictive models. 相似文献
11B and 27Al magic angle spinning nuclear magnetic resonance (MAS NMR) spectra of alkaline-earth boroaluminate glasses show that the structure of these glasses are far more complicated than previously thought. The relative concentrations of 3- and 4-coordinated boron vary as found by previous investigators using continuous-wave NMR methods, but the 27Al NMR spectra indicate the presence of Al in 4-, 5-, and 6-fold coordination, in contrast to previous assignments. Analysis of the data based on local charge balance considerations provides a qualitative model that correctly predicts compositional variations of the NMR peak intensities and 27Al chemical shifts for a wide range of boroaluminate glass compositions. 相似文献
Studies of defined mixtures of carcinogenic polycyclic aromatic hydrocarbons (PAH) have identified three major categories of interactions: antagonism; synergism; and additivity depending on the biological model, tissue, route of exposure, and specific PAH. To understand the bases of these interactions we studied binary mixtures of benzo[a]pyrene (B[a]P) and dibenz[a,h]anthracene (DBA) in transformable C3H10T1/2C18 (C3H10T1/2) mouse embryo fibroblast cells in culture. C3H10T1/2 cells treated with binary mixtures of B[a]P and DBA gave less than additive morphological cell transformation based on response additivity. These results were consistent with those reported in mice and rats on the antagonistic effects of B[a]P and DBA on tumorigenesis. 32P-Postlabeling DNA adduct studies revealed that DBA reduced B[a]P-DNA adduct levels by 47% with no effect on DBA-DNA adduct levels. This suggests that one mechanism for the inhibition of morphological cell transformation of binary mixtures of B[a]P and DBA is due to alterations in the metabolic activation of B[a]P. 相似文献
The synthesis of the title complexes was achieved via the reaction of
-p-dichlorobenzene-
-cyclopentadienyliron cations with 4,4′-bis(4-hydroxyphenyl)valeric acid to produce the diiron complexes which were then reacted with a number of arylazo dyes to give cationic bis(cyclopentadienyliron)arene complexes containing the arylazo dyes. These iron-containing monomers were subsequently polymerized via nucleophilic aromatic substitution using 1,8-octanedithiol, 4,4′-thiobisbenzenethiol, or bisphenol A to produce the desired coloured cationic organoiron polymers. The weight – average molecular weights were estimated to range from 11,800 to 31,600. UV–vis studies conducted in dimethylformamide (DMF) showed that the metallated polymers exhibited
of 412–491 nm. Addition of HCl to the polymer solution caused a bathochromic shift into the range of 515–530 nm. Thermogravimetric analysis (TGA) revealed that the iron moieties were cleaved between 205 and 248 °C while the polyether/thioether backbone degraded between 380 and 613 °C. Differential scanning calorimetry (DSC) showed that the polymers exhibited glass transition temperatures (Tg) ranging from 106 to 184°C.This paper is dedicated to Professor Richard J. Puddephatt in recognition of his outstanding contribution to the field of metal-containing polymers. 相似文献
Amongst the different perovskites being investigated for application in solar cells, one of the most frequently scrutinized is methylammonium lead iodide CH3NH3PbI3 (or MAPbI3), which is usually obtained by the reaction of lead iodide (PbI2) with methylammonium iodide (MAI). Although this perovskite has been extensively studied and utilized in the manufacture of high-efficiency solar cells, its formation chemistry is still not well understood. Reliable experimental determination of the activation energy between PbI2 and MAI has been difficult due to the rapid reaction at room temperature. In this work, we determined the activation energy by adopting the Arrhenius equation. This was possible by controlling the reaction using MAI vapor, instead of liquid solution. This procedure allowed the reaction to be carried out at temperatures of up to 150 °C. The formation of MAPbI3 films was obtained by a two-step process: deposition of thin PbI2 film by thermal evaporation and subsequent conversion into perovskite by exposure to MAI vapor. The conversion of PbI2 to MAPbI3 as a function of temperature was probed by X-ray diffraction. An activation energy of 0.12?±?0.02 eV was obtained. This low value explains the ease of MAPbI3 formation at low temperatures, and partially explains its instability in environmental conditions.
Many of the electrical failures of large electric machines have mechanical precursors. This premise has led to the attempts described here to detect mechanical changes, such as groundwall delamination, by acoustic methods as a means of early detection of incipient failure. By optimally launching an ultrasonic wave into a stator bar and using the conductor as a waveguide, it has been shown possible to interrogate the groundwall insulation and the critical interface region adjacent to the conductor. Laboratory studies using an epoxy mica stator bar subjected to thermal cycling have demonstrated that the acoustic signatures obtained with this method are mirrored by conventional corona spectroscopy conducted simultaneously, although earlier damage is clearly discernible. Based on the results of this study, the acoustic technique appears to have substantial promise as an advanced detection tool 相似文献