Absolute interferometry with a 670-nm external cavity diode laser

In the past few years there has been much interest in use of tunable diode lasers for absolute interferometry. Here we report on use of an external cavity diode laser operating in the visible (lambda ~ 670 nm) for absolute distance measurements. Under laboratory conditions we achieve better than 1-mum standard uncertainty in distance measurements over a range of 5 m, but significantly larger uncertainties will probably be more typical of shop-floor measurements where conditions are far from ideal. We analyze the primary sources of uncertainty limiting the performance of wavelength-sweeping methods for absolute interferometry, and we discuss how errors can be minimized. Many errors are greatly magnified when the wavelength sweeping technique is used; sources of error that are normally relevant only at the nanometer level when standard interferometric techniques are used may be significant here for measurements at the micrometer level.     

Reactant partitioning in free-radical heterophase polymerization: The case of inverse microemulsion polymerization of acrylamide

Conversion curves have been determined at 60°C for the polymerization of acrylamide in percolating inverse microemulsions. Ammonium peroxo-disulphate (APS) and dibenzoyl peroxide (DBP) were used as initiators of free-radical polymerization in the presence or absence of potassium nitrosodisulphonate (Fremy's salt, FS). The percolation decreases the rate of polymerization of acrylamide initiated by APS. The polymerization is inhibited by FS. After an inhibition period, retardation of acrylamide polymerization is more pronounced in non-percolating microemulsions. No inhibition periods were observed for DBP-initiated polymerization of acrylamide. The percolation shortens the time interval of the ‘slow’ polymerization of acrylamide, but the rates of rapid acrylamide polymerization above 10% conversion are the same for percolating and for non-percolating inverse microemulsions. The polymer particle diameter is a function of acrylamide/water weight ratio and of [water]/[AOT] (AOT: bis(2-ethylhexyl)-sulphosuccinate sodium salt) molar ratio. No effect of the initiator's nature either in the presence or in the absence of FS was found. The results are interpreted on the basis of initiator and/or nitroxide radical partitioning between oil and water phases of the inverse microemulsion, and are discussed with respect to the mechanism of acrylamide polymerization and polymer particle formation proposed for non-percolating inverse microemulsions.     

Poly(methyl methacrylate) and polyacrylonitrile dispersions stabilized by gelatin

Methyl methacrylate was polymerized in an aqueous medium in the presence of gelatin using potassium persulfate as initiator. The dispersion mode of polymerization, when the monomer is completely miscible with water, was investigated and compared with an emulsion process, which proceeds at higher monomer concentration. Spherical and relatively uniform polymer particles were formed. Macroscopic precipitation of polymer is prevented by combination of the steric stabilization by grafted gelatin and of repulsive electrostatic interactions from the initiator residues attached to the particle surface. Static and dynamic light scattering have been used to determine the molar mass (molar mass of the whole dispersion particle, M_wD ～ 10⁸-10⁹ g mol^?1) and hydrodynamic radius (R_hD ～ 50-120 nm) of the particles. The number of particles per unit volume does not depend on overall monomer concentration, and it is higher, and therefore the particle size is smaller, than that observed for the soapless emulsion polymerization. The addition of gelatin may be thus used to modify the particle size. Acrylonitrile dispersions were prepared under similar conditions. Unlike methyl methacrylate, this monomer does not swell the polymer particles. While poly(methyl methacrylate) particles are spherical and relatively uniform, the polyacrylonitrile dispersions consist of polydisperse aggregates of tiny polymer particles.     

Influence of oxygen partial pressure and substrate temperature during vapour deposition on the structural properties of CdSe films

CdSe films prepared in vacuum by sublimation from the compound at oxygen partial pressures in the residual atmosphere from 2.8 × 10^?5 to 3.2 × 10^?4 Torr and at substrate temperatures of 295 and 523 K were subjected to X-ray structural analysis. The results obtained are analysed and discussed in terms of some structures different from those of CdSe, e.g. CdSeO₃ and CdSeO₃.SeO₂.     

Aldehyde functionalization of styrene polymers

Summary Two methods of the introduction of aldehyde group into polystyrene skeleton are described.     

Toxicity increases in ice containing monochlorophenols upon photolysis: environmental consequences

The toxic effects of photoproducts formed upon the photolysis of 2- and 4-chlorophenol (CP) frozen solutions in polycrystalline ice phase were determined with a bacterial luminescence test (Vibrio fisheri), and in vitro biomarker assay for dioxin-like effects (inductions of AhR-dependent luciferase in H4IIE-luc cells) and compared to the toxic effects of products of the same photoreaction in aquatic phase. Coupling photoproducts formed in ice samples (3'-chlorobiphenyl-2,4'-diol and 3-chlorobiphenyl-2,2'-diol from 2-CP photolysis and 5-chlorobiphenyl-2,4'-diol from 4-CP photolysis) were found to be more toxic to V. fisheri than parent CPs and elicited significant inductions of dioxin-like effects (the effective concentrations EC50 approximately 3 x 10(-5) mol L(-1) corresponded to known weaker ligands of AhR, such as nonplanar polychlorinated biphenyls or polycyclic aromatic hydrocarbons). To complete the picture, a photoproduct formed from 4-CP (5-chlorobiphenyl-2,4'-diol) was synthesized, and a detailed toxicity assessment with purified compound confirmed the results obtained with irradiated samples. Our findings support a recently proposed model according to which solar radiation can trigger the formation of new types of organic pollutants in polar ice or tropospheric ice cloud particles, presenting possibly greater risk to the environment than the parent compounds.     

Czech results at criticality dosimetry intercomparison 2002

Two criticality dosimetry systems were tested by Czech participants during the intercomparison held in Valduc, France, June 2002. The first consisted of the thermoluminescent detectors (TLDs) (Al-P glasses) and Si-diodes as passive neutron dosemeters. Second, it was studied to what extent the individual dosemeters used in the Czech routine personal dosimetry service can give a reliable estimation of criticality accident exposure. It was found that the first system furnishes quite reliable estimation of accidental doses. For routine individual dosimetry system, no important problems were encountered in the case of photon dosemeters (TLDs, film badge). For etched track detectors in contact with the 232Th or 235U-Al alloy, the track density saturation for the spark counting method limits the upper dose at approximately 1 Gy for neutrons with the energy >1 MeV.     

Static load balancing applied to Schur complement method

A finite element method often leads to large sparse symmetric and positive definite systems of linear equations. We consider parallel solvers based on the Schur complement method on homogeneous parallel machines with distributed memory. A finite element mesh is partitioned by graph partitioning. Such partitioning results in submeshes with similar numbers of elements and, consequently, submatrices of similar sizes. The submatrices are partially factorised. The time spent on the partial factorisation can be different, i.e., disbalanced, because methods exploiting the sparsity of submatrices are used. This paper proposes a Quality Balancing heuristic that modifies classic mesh partitioning so that the partial factorisation times are balanced, which saves overall computation time, especially for time dependent mechanical and nonstationary transport problems.     

Variation in fatty acid composition of ewes' milk during continuous transition from dry winter to natural pasture diet

The profile variations of approximately 70 fatty acids (FAs) in milk of ewes consuming total mixed rations (TMR) and grazing natural pasture were determined. Milk of ewes grazing pasture in May and September in the Slovak Republic contained 3-times more conjugated linoleic acid (CLA) (P < 0.001) and trans-vaccenic acid (TVA) (P < 0.001), and 2-times more α-linolenic acid (ALA) (P < 0.001) than that of ewes fed TMR. A doubling of the CLA and TVA contents of milk of ewes fed with TMR was achieved by changing to meadow hay containing a higher ALA content. Less availability of vegetation and lower ALA pasture content in summer (P < 0.001) caused a 2-fold decrease (P < 0.001) of CLA and TVA contents when compared with data obtained in May. With grass re-growth and an increase in pasture ALA content in September, the CLA and TVA contents rose to values similar to those obtained in May (P > 0.05). No significant differences in the FA composition in milk of ewes grazing on summer pasture at higher altitude were observed.