Mode coupling contribution to radiation losses in curvatures for high and low numerical aperture plastic optical fibers

We have studied the optical power losses due to multiple curvatures in polymethylmetacrylate (PMMA) plastic optical fibers (POFs) of different numerical apertures (NAs) and attenuation. The fibers were tested for several configurations in order to assess the influence of different types of curved-to-straight fiber transitions in the amount of power radiation. We found that losses are below the standards for all tested fiber types, and thus, they are a suitable choice for local area network (LAN) applications. In addition, our results revealed the presence of modal interactions as confirmed using an experimental procedure to estimate the mode coupling strength for the same fibers.     

Automated estimation of rock fragment distributions using computer vision and its application in mining

Size distribution of rock fragments obtained from blasting and crushing in the mining industry has to be monitored for optimal control of a variety of processes before reaching the final grinding, milling and the froth flotation processes. Whenever feasible, mechanical sieving is the routine procedure to determine the cumulative rock weight distribution on conveyor belts or free falling off the end of transfer chutes. This process is tedious and very time consuming, even more so if a complete set of sieving meshes is used. A computer vision technique is proposed based on a series of segmentation, filtering and morphological operations specially designed to determine rock fragment sizes from digital images. The final step uses an area-based approach to estimate rock volumes. This segmentation technique was implemented and results of cumulative rock volume distributions obtained from this approach were compared to the mechanical fragment distributions. The technique yielded rock distribution curves which represents an alternative to the mechanical sieving distributions.     

Structural conversions of rhodamines in solution

A study has been made of the acidic ionization, structural conversions, and prototropic tautomerism of rhodamine chromogens in methanol and dimethyl sulfoxide, using IR, ¹³ C NMR, and electronic spectroscopy. The lactone structure has been established for the colorless form of rhodamines in DMSO. For rhodamine B in mixtures of water with DMSO, the lactone/zwitterion ratio has been estimated.V. I. Vernadskii Institute of Geochemistry and Analytical Chemistry, Russian Academy of Sciences, Moscow 117975. Khar'kov State University, Khar'kov 310077. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 3, pp. 512–521, March, 1992.     

Crystallographic orientation dependence of the growth rate for GaAs low pressure organometallic vapor phase epitaxy

The complete crystallographic orientation dependence of the growth rate for GaAs low pressure organometallic vapor phase epitaxy (LPOMVPE) is determined using a previously described semi-empirical model. A set of LPOMVPE growth rate polar diagrams is presented for reactor temperatures near 550°C as well as near 700°C. Also, the variation of the growth rate polar diagrams as a function of process variables is given. The experimental data utilized in the semiempirical model was attained using a typical horizontal reactor LPOMVPE system and typical LPOMVPE process parameters.     

Commutators of singular integrals on spaces of homogeneous type

In this work we prove some sharp weighted inequalities on spaces of homogeneous type for the higher order commutators of singular integrals introduced by R. Coifman, R. Rochberg and G. Weiss in Factorization theorems for Hardy spaces in several variables, Ann. Math. 103 (1976), 611–635. As a corollary, we obtain that these operators are bounded on L ^p (w) when w belongs to the Muckenhoupt’s class A _p , p > 1. In addition, as an important tool in order to get our main result, we prove a weighted Fefferman-Stein type inequality on spaces of homogeneous type, which we have not found previously in the literature.     

Compressible dimer model for the phase trasition in SnCl2·2H2O

The basic dimer model for the phase transition in the layered hydrogen-bonded crystal SnCl₂·2H₂O is modified by the inclusion of elastic effects. This compressible dimer model, in which the dimer excitation energy depends on lattice volume, is used to explain the anomalous specific-heat data close to the transition temperature.     

Thermal and spectroscopic study of the solid complexes of furan-2-hydroxamic acid and several divalent metallic cations

Solid crystalline complexes of furan-2-hydroxamic acid (FHA) and six metallic divalent cations (Ca(II), Ba(II), Co(II), Ni(II), Cu(II), and Cd(II)) were prepared. In all cases the stoichiometry was 2(FHA)1 (cation). The solids were characterized by elemental analysis, TG, DSC and IR techniques.

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Zusammenfassung Es wurden feste, kristalline Komplexe von Furan-2-hydroxamsäure (FHA) und sechs verschiedenen bivalenten Metallkationen hergestellt: Ca(II), Ba(II), Co(II), Ni(II), Cu(II) und Cd(II). Die stöchiometrische Zusammensetzung betrug in allen Fällen 2(FHA)1(Kation). Die Feststoffe wurden mittels Elementaranalyse, TG-, DSC- und IR-Techniken charackterisiert.

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Photochemically induced fluorescence investigation of aβ-cyclodextrin: Azure A inclusion complex and determination of analytical parameters

The photooxidation of Azure A and fluorescence properties of Azure A and its photoproduct have been investigated in aqueous media and in the presence of-cyclodextrin (-CD). The fluorescence intensity of the complex formed between the photoproduct and -CD was found to be three times higher than that of the uncomplexed Azure A photoproduct. A complex formation constant of 110±40 M^–1 was calculated using the Benesi-Hildebrand treatment of the fluorescence emission data. Although the stoichiometry of the Azure A photoproduct: -CD complex was found to be 1: 1, it seems that the Azure A structure is only partially included. Calibration graphs were plotted for the free Azure A photoproduct and the photogenerated product included in -CD. The analytical parameters and quantification limits were determined.     

Extraction--spectrophotometric determination of oxalate in urine and blood serum

An extraction--spectrophotometric method is described for the determination of oxalate, based on the formation of a mixed ligand vanadium (V)--mandelohydroxamic acid--oxalate complex. The complex was extracted into a solution of trioctylmethylammonium chloride (Adogen 446) in toluene and the absorbance measured at 535 nm. The experimental variables and interferences in this determination were studied. The detection limit is 0.5 microgram ml-1 and the range of application is between 2 and 8 micrograms ml-1. The method was applied to the determination of oxalate in urine and blood serum.