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Experiments by Gittings, Bandyopadhyay and Durian (Europhys. Lett. 65, 414 (2004)) demonstrate that light possesses a higher probability to propagate in the liquid phase of a foam due to total reflection. The authors term this observation photon channelling which we investigate in this article theoretically. We first derive a central relation in the work of Gitting et al. without any free parameters. It links the photon's path-length fraction f in the liquid phase to the liquid fraction ɛ. We then construct two-dimensional Voronoi foams, replace the cell edges by channels to represent the liquid films and simulate photon paths according to the laws of ray optics using transmission and reflection coefficients from Fresnel's formulas. In an exact honeycomb foam, the photons show superdiffusive behavior. It becomes diffusive as soon as disorder is introduced into the foams. The dependence of the diffusion constant on channel width and refractive index is explained by a one-dimensional random-walk model. It contains a photon channelling state that is crucial for the understanding of the numerical results. At the end, we shortly comment on the observation that photon channelling only occurs in a finite range of ɛ.  相似文献   
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The use of infrared laser-assisted fluorination to release oxygen from milligram quantities of silicates or other oxide mineral grains is a well-established technique. However, relatively few studies have reported the optimisation of this procedure for oxygen-17 isotope measurements. We describe here details of an analytical system using infrared (10 μm) laser-assisted fluorination, in conjunction with a dual inlet mass spectrometer of high resolving power ( approximately 250) to provide (17)O and (18)O oxygen isotope measurements from 0.5-2 mg of silicates or other oxide mineral grains. Respective precisions (1) of typically 0.08 and 0.04 per thousand are obtained for the complete analytical procedure. Departures from the mass-dependent oxygen isotope fractionation line are quantified by Delta(17)O; our precision (1) of such measurements on individual samples is shown to be +/-0.024 per thousand. In turn, this permits the offset between parallel, mass-dependent fractionation lines to be characterised to substantially greater precision than has been possible hitherto. Application of this system to investigate the (17)O versus (18)O relationship for numerous terrestrial whole-rock and mineral samples, of diverse geological origins and age, indicates that the complete data set may be described by a single, mass-dependent fractionation line of slope 0.5244+/- 0.00038 (standard error). Copyright 1999 John Wiley & Sons, Ltd.  相似文献   
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Fast atom bombardment, combined with high-energy collision-induced tandem mass spectrometry, has been used to investigate gas-phase metal-ion interactions with captopril, enalaprilat and lisinopril, all angiotensin-converting enzyme inhibitors.Suggestions for the location of metal-binding sites are presented. For captopril, metal binding occurs most likely at both the sulphur and the nitrogen atom. For enalaprilat and lisinopril, binding preferably occurs at the amine nitrogen. Copyright 1999 John Wiley & Sons, Ltd.  相似文献   
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Reactive quenching of OH(A 2Sigma+,v=0) by D2 forming HOD+D was studied in crossed molecular beams. The D atom products are primarily forward scattered relative to the incident D2. The dominant mechanism involves a direct reaction from relatively large impact parameters with approximately 88% of the available energy appearing in HOD internal excitation.  相似文献   
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The effects on the radiation response of Harwell polymethylmethacrylate (PMMA) dosimeters of dose-rate, radiation type, temperature during irradiation and post-irradiation storage, and post-irradiation stability, are of importance to the operators of commercial irradiation facilities.

This paper describes recent studies of the effects of some of these parameters on the radiation response of Harwell Red 4034, Amber 3042, and Gammachrome YR Perspex dosimeters, and provides data on batch to batch variation and shelf-life.  相似文献   

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We have used oxygen Rydberg time-of-flight spectroscopy to carry out a crossed molecular beam study of the CN + O2 reaction at collision energies of 3.1 and 4.1 kcal/mol. The O(3P2) products were tagged by excitation to high-n Rydberg levels and subsequently field ionized at a detector. The translational energy distributions were broad, indicating that the NCO is formed with a wide range of internal excitation, and the angular distribution was forward-backward symmetric, indicating the participation of NCOO intermediates with lifetimes comparable to or longer than their rotational periods. Rice-Ramsperger-Kassel-Marcus modeling of the dissociation of NCOO to NCO + O suggests that Do(NC-OO) > or = 38 kcal/mol, which is consistent with several theoretical calculations. Implications for the competing CO + NO channel are discussed.  相似文献   
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In this paper, we analyze the sensitivity enhancement attainable by combining a wavelength modulation (WM) technique to integrated cavity output spectroscopy (ICOS), pointing out how the spectrometer??s parameters and the acquisition strategy affect the detection noise in both techniques. We point out that WM-ICOS is mainly limited by the slow scan rate that it requires, compared to regular ICOS. Nevertheless, according to our analysis, WM can still appreciably improve the SNR of an ultrasensitive ICOS system, if the cavity transmission is so low that the detector noise is not negligible. In light of these considerations, we directly compare the performance of ICOS and WM-ICOS in a high sensitivity ambient-air methane detection experiment, finding a good agreement with the theoretical influence of the various spectrometer parameters.  相似文献   
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Oxygen Rydberg time-of-flight spectroscopy was used to study the vacuum ultraviolet photodissociation dynamics of N(2)O near 130 nm. The O((3)P(J)) products were tagged by excitation to high-n Rydberg levels and subsequently field ionized at a detector. In agreement with previous work, we find that O((3)P(J)) formation following excitation to the repulsive N(2)O D((1)Sigma(+)) state produces the first two electronically excited states of the N(2) counterfragment, N(2)(A (3)Sigma(u) (+)) and N(2)(B (3)Pi(g)). The O((3)P(J)) translational energy distribution reveals that the overall branching ratio between N(2)(A (3)Sigma(u) (+)) and N(2)(B (3)Pi(g)) formation is approximately 1.0:1.0 for J = 1 and 2, with slightly less N(2)(B (3)Pi(g)) produced in coincidence with O((3)P(0)). The angular distributions were found to be independent of J and highly anisotropic, with beta = 1.5+/-0.2.  相似文献   
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