Effect of a water film on the structure of ice growing beneath it

It is demonstrated that ice growing beneath a water film may take on either a transparent or an opaque form, depending on the thickness of the water film.Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 33, No. 2, pp. 323–328, August, 1977.     

Geometric determination of saturation in fluorescence spectroscopy

In laser spectroscopy, saturation of atomic or molecular transitions cannot be ignored, even at modest laser intensities. The saturation status is customarily diagnosed from measurements of saturation curves describing the dependence of spectroscopic signals on laser intensity. I propose an alternative method that relies on a geometric comparison of the spatial laser profile with images of the spectroscopic quantity under investigation. A single image can be used to determine the saturation status and its associated saturation laser intensity.     

Thickness determination of ultrathin metal films using the X-ray fluorescence technique

The X-ray fluorescence technique was used to determine the thickness of single-layered, double-layered and triple-layered films of copper, bismuth and gold on mylar substrates. An annular ¹⁰⁹Cd X-ray source of 5 mCi was used to excite hte characteristic X-rays. The background was much lower as well as flat in the present study in comparison with our earlier results an ²⁴¹Am exciter source. This resulted in a downward extension of the lower limit of thickness measurement of thin films coupled with an improved accuracy.     

On-line determination of oxygen isotope ratios of water or ice by mass spectrometry

Oxygen isotope ratio determination on any of the water phases (water vapor, water, ice) is of great relevance in different research fields such as climate and paleoclimate studies, geological surveys, and hydrological studies. The conventional technique for oxygen isotope measurement involves equilibration with carbon dioxide gas for a given time with a subsequent isotope determination. The equilibration technique is available in different layouts, but all of them are rather time-consuming. Here we report a new on-line technique that processes water samples as well as ice samples. The same principal, CO2 hydration, is used but speeded up by (i) a direct injection and full dissolution of CO2 in the water, (ii) an increased isotope exchange temperature at 50 degrees C, and (iii) a rapid gas extraction by means of an air-permeable membrane into a continuous helium flux supplying the isotope ratio mass spectrometer with the sample gas. The precision is better than 0.1/1000 which is only slightly larger than with the conventional equilibration technique. This on-line technique allows analysis of 1 m of ice with a resolution of 1-3 cm, depending on the meltwater flux, within 1 h. Similarly, continuous and fast analysis can be performed for aqueous samples for hydrological, geological, and perhaps medical applications.     

Random lasing in a dye-doped polymer thin film waveguide deposited on a Si surface microstructured by femtosecond laser ablation

Random laser action with ~8 nm of bandwidth from a special waveguide structure is reported. The waveguide structure is composed of a layer of rhodamine 6G-doped PMMA film and a silicon substrate with a microstructured surface induced by a femtosecond laser. The silicon substrate featured two-dimensional island-like microstructures with average sizes ranging from 0.8 μm to 3 μm and average heights at about 0.7 μm. A red-shift of laser peak positions and decrease of threshold were observed with decreasing size of silicon surface microstructures. The spectra at different probe directions were also measured, and the results reveal that the waveguide laser action is strongly confined within ±10° from the direction of the edge. The lasing modes emitted from the edge of the waveguide are found to be mainly transverse electric-polarized. Our experiments demonstrate a promising method to achieve waveguide random lasers.     

Bandgap determination of P(VDF-TrFE) copolymer film by electron energy loss spectroscopy

The ferroelectric β of poly(vinylidene fluoride trifluoroethylene), P(VDF-TrFE) is confirmed for 100 nm thickness spin coated copolymer film. The homogeneous coverage of the copolymer film is investigated by the help of X-ray photoelectron spectroscopy (XPS). Most importantly, the existing bandgap in the crystalline phase of the copolymer is determined directly from the electron energy loss spectroscopy (EELS).     

Investigation of nonionic diazo dye-doped polymer dispersed liquid crystal film

Sudan black B (SBB) was used to investigate as the nonionic diazo dye-doped in polymer dispersed liquid crystal (PDLC) display, by polymerization-induced phase separation (PIPS) method. The maximum absorbance, contrast ratio, dichroic ratio and the order parameter of nonionic diazo dye in nemetic host (TL203) were investigated using UV?CVis polarized spectroscopy. The orientation of the dye molecules was controlled by electric field, which enabled the contrast ratio of the dye to be obtained by electrically switching. The change occurring on droplet morphologies and electro-optical properties of PDLC film with the change in contents of Sudan black dye and liquid crystals (LC) contents was investigated. We found an increase in LC droplet sizes with the increase of diazo dye and LC contents. Moreover the addition of small amount of nonionic diazo dye reduced the threshold voltage (V $_{\boldsymbol{\rm th}})$ , increased off-state transmittance, enhanced the contrast ratio and decreased the response time of dye-doped PDLC. Additionally the change in transition temperature of LC and changes in LC droplet morphologies with the addition of dye were also observed. Such changes were observed with the images taken by polarized optical microscope (POM). The detail discussions on such behaviours were also made.     

Analysis of water ice and water ice/soil mixtures using laser-induced breakdown spectroscopy: application to Mars polar exploration

Recently, laser-induced breakdown spectroscopy (LIBS) has been developed for the elemental analysis of geological samples for application to space exploration. There is also interest in using the technique for the analysis of water ice and ice/dust mixtures located at the Mars polar regions. The application is a compact instrument for a lander or rover to the Martian poles to interrogate stratified layers of ice and dusts that contain a record of past geologic history, believed to date back several million years. Here we present results of a study of the use of LIBS for the analysis of water ice and ice/dust mixtures in situ and at short stand-off distances (< 6.5 m) using experimental parameters appropriate for a compact instrument. Characteristics of LIBS spectra of water ice, ice/soil mixtures, element detection limits, and the ability to ablate through ice samples to monitor subsurface dust deposits are discussed.     

Impact by pressure waves on a vapor film during film boiling of subcooled water

We investigated experimentally the interaction of pressure waves with a vapor film during film boiling of subcooled water on the surface of solid spheres. We observed a change in the interphase surface image under the impact by those waves. We noted the similarity of the observed phenomena with those registered under the absence of any external influence on the process.     

Photophysics of laser dye-doped polymer membranes for laser-induced fluorescence photogrammetry

Laser-induced fluorescence target generation in dye-doped polymer films has recently been introduced as a promising alternative to more traditional photogrammetric targeting techniques for surface profiling of highly transparent or reflective membrane structures. We investigate the photophysics of these dye-doped polymers to help determine their long-term durability and suitability for laser-induced fluorescence photogrammetric targeting. These investigations included experimental analysis of the fluorescence emission pattern, spectral content, temporal lifetime, linearity, and half-life. Results are presented that reveal an emission pattern wider than normal Lambertian diffuse surface scatter, a fluorescence time constant of 6.6 ns, a pump saturation level of approximately 20 microJ/mm2, and a useful lifetime of more than 300,000 measurements. Furthermore, two demonstrations of photogrammetric measurements by laser-induced fluorescence targeting are presented, showing agreement between photogrammetric and physically measured dimensions within the measurement scatter of 100 microm.     

Study on ice slurry production by water spray

A theoretical and experimental study was performed to examine the water spray method of ice slurry production. First, the conditions for the formation of ice particles were investigated theoretically by the diffusion-controlled evaporation model. The prediction of the model was proved to agree relatively well with experiments in which we examined the conditions for a droplet of initial temperature 20°C and size 50 μm to change into an ice particle in a chamber of height 1.33 m. Second, the production of cold storage heat will increase almost proportionally to the number of spray nozzles because no substantial difference was found in the Sauter Mean Diameter (SMD) of sprays from single and twin nozzle. Third, an ice slurry was experimentally obtained by spraying droplets of 7% ethylene glycol aqueous solution in a vacuum chamber where pressure is maintained below the freezing point of the solution. Finally, based on the theoretical and experimental results, we propose an optimizing chart for providing the operating conditions to make ice slurry using the relations of the staying time of the droplet in the chamber, the injection pressure, the spray droplet size and the chamber pressure.     

On the determination of dopant-concentration profiles by grazing emission X-ray fluorescence spectroscopy using the maximum-entropy method

The determination of concentration profiles of impurities in silicon from angle scans of emitted x-ray fluorescence intensities using the maximum-entropy method is studied. Existence and convergence properties of the maxium- entropy method are discussed. The application of the maximum-entropy method to Grazing emission X-Ray Fluorescence Spectromety is compared with an analytical method. It is found that, provided noise levels are sufficiently low, concentration profiles can be reconstructed without using a priori knowledge.     

Confined diffusion in tubular structures analyzed by fluorescence correlation spectroscopy on a mirror

In fluorescence correlation spectroscopy (FCS) analysis it is generally assumed that molecular species diffuse freely in volumes much larger than the three-dimensional FCS observation volume. However, this standard assumption is not valid in many measurement conditions, particularly in tubular structures with diameters in the micrometer range, such as those found in living cells (organelles, dendrites) and microfluidic devices (capillaries, reaction chambers). As a result the measured autocorrelation functions (ACFs) deviate from those predicted for free diffusion, and this can shift the measured diffusion coefficient by as much as ~50% when the tube diameter is comparable with the axial extension of the FCS observation volume. We show that the range of validity of the FCS measurements can be drastically improved if the tubular structures are located in the close vicinity of a mirror on which FCS is performed. In this case a new fluctuation time in the ACF, arising from the diffusion of fluorescent probes in optical fringes, permits measurement of the real diffusion coefficient within the tubular structure without assumptions about either the confined geometry or the FCS observation volume geometry. We show that such a measurement can be done when the tubular structure contains at least one pair of dark and bright fringes resulting from interference between the incoming and the reflected excitation beams on the mirror surface. Measurement of the diffusion coefficient of the enhanced green fluorescent protein (EGFP) and IscS-EGFP in the cytoplasm of living Escherichia coli illustrates the capabilities of the technique.     

Nondestructive varnish identification by ultraviolet fluorescence spectroscopy

The identification of the chemical nature of varnish is essential for art restorers in order to choose a suitable solvent during its removal. Until today, such identification has been performed using chemical analysis after sampling. An innovative technique is presented here, using ultraviolet (UV) fluorescence spectroscopy. The method is nondestructive, workable in situ, and leads to results in real time. It is based on the comparison between the emission spectrum of an unknown varnish with those of fresh, artificially aged, or old reference resins and varnishes, for different monochromatic excitation wavelengths. The resin and the nature of the varnish as spirit, oil, or mixed can thus be identified. Various examples are presented on home-made samples applied on fluorescent backgrounds and on real works of art.     

Determination of the elastic properties of a barrier film on aluminium by Brillouin spectroscopy

The surface wave dispersion for a barrier oxide film on aluminium has been determined from surface Brillouin scattering measurements carried out on films of thicknesses of 0.2, 0.35 and 0.45 μm. The measured velocities of the generalised Rayleigh mode, the pseudo interfacial mode and of several Lamb modes conform to simulations performed for stiffening layers [1]. The longitudinal velocity and the shear velocity of the layer have been calculated from the experimental dispersion curve.     

Simultaneous enantiomeric determination of dansyl-D,L-phenylalanine by fluorescence spectroscopy in the presence of alpha-acid glycoprotein.

Few techniques are amenable to real-time analysis of enantiomers. In this paper, total complexation by alpha-acid glycoprotein (AGP) is shown to discriminate between enantiomers of dansyl-D,L-phenylalanine (DPs) by changing the local environment of the D and L enantiomers (DDP and DLP, respectively) from hydrophilic to hydrophobic. DDP and DLP show the same native fluorescence at lambda ex/lambda em = 200/544 nm in the absence of AGP, but show shifted emissions with a component at lambda ex/lambda em = 220/497 nm in the presence of AGP and in lipophilic solutions. The conditions for an analytical determination have been optimized, and the method has been used to measure the enantiomeric composition of DDP/DLP mixtures with concentration ratios varying over 2 orders of magnitude. The mechanism of chiral recognition for DDP and DLP by AGP is discussed and should be equally applicable to other dansyl-derivative amino acid enantiomers. The association constants for AGP with DDP and with DLP have been determined to be 1.33 x 10(2) L g-1 and 2.29 x 10(2) L g-1, respectively.     

Investigation of asphaltene association by front-face fluorescence spectroscopy

The tendency of asphaltenes to aggregate and form clusters in solvents was studied by fluorescence spectroscopy. This was done by evaluating the relative fluorescence quantum yield of asphaltenes diluted at several concentrations in toluene and by studying the changes in the fluorescence spectra of asphaltene solutions as the composition of the solvent, toluene and cyclohexane, is changed. The asphaltene fraction (heptane insoluble) was collected from a Brazilian heavy crude oil, and solutions of this material varying from 0.016 g/L up to 10 g/L were prepared in toluene. Front-face emission spectra were obtained in two wavelength ranges, from 310 to 710 nm, excited at 300 nm (short range), and from 410 to 710 nm, excited at 400 nm (long range). Severe quenching was observed at concentrations above about 0.1 g/L. Stern-Volmer plots (reciprocal of quantum yield against concentration) exhibited nonlinear, downward-curved behavior, indicating that a more complex suppression mechanism, probably influenced by the association of the asphaltene molecules, is taking place. The same asphaltenes were dissolved (0.1 g/L) in binary mixtures of toluene and cyclohexane, and emission spectra in both the short range and long range were obtained. Fluorescence was progressively quenched at longer wavelengths of the spectra as the proportion of cyclohexane in the solvent grew. Cyclohexane, a poor asphaltene solvent, is probably inducing static quenching through association of asphaltenes.     

Convective-diffusion-based fluorescence correlation spectroscopy for detection of a trace amount of E. coli in water

Fluorescence correlation spectroscopy (FCS) is adapted for a new procedure to detect trace amounts of Escherichia coli in water. The present concept is based on convective diffusion rather than Brownian diffusion and employs confocal microscopy as in traditional FCS. With this system it is possible to detect concentrations as small as 1.5 x 10(5) E. coli per milliliter (2.5 x 10(-16) M). This concentration corresponds to an approximately 1.0-nM level of Rhodamine 6G dyes. A detailed analysis of the optical system is presented, and further improvements for the procedure are discussed.