Accommodation of large plastic strains and defect accumulation in nanocrystalline Ni grains

A transmission electron microscopy (TEM) study has been carried out to uncover how dislocations and twins accommodate large plastic strains and accumulate in very small nanocrystalline Ni grains during low-temperature deformation. We illustrate dislocation patterns that suggest preferential deformation and nonuniform defect storage inside the nanocrystalline grain. Dislocations are present in individual and dipole configurations. Most dislocations are of the 60 degrees type and pile up on (111) slip planes. Various deformation responses, in the forms of dislocations and twinning, may simultaneously occur inside a nanocrystalline grain. Evidence for twin boundary migration has been obtained. The rearrangement and organization of dislocations, sometimes interacting with the twins, lead to the formation of subgrain boundaries, subdividing the nanograin into mosaic domain structures. The observation of strain (deformation)-induced refinement contrasts with the recently reported stress-assisted grain growth in nanocrystalline metals and has implications for understanding the stability and deformation behavior of these highly nonequilibrium materials.

Diagnóstico de la brucelosis bovina por el método del "ring-test"

El presente trabajo se llevó a cabo entre los meses de Julio a Septiembre del año 1965, en los Laboratorios de la Escuela Nacional de Agricultura y Ganadería. Se recurrió a la prueba del Ring-Test, para diagnosticar la Brucelosis en hatos situados en los departamentos de Managua, León, Carazo, Masaya, Granada, Rivas y Boaco; se obtuvieron ciertos datos estadísticos al objeto de hacer un estudio de productividad de leche. Los resultados de este trabajo fueron: 1). Las fincas positivas se encuentran localizadas en los departamentos de Managua, Carazo, Granada y Rivas. 2). Los porcentajes de hatos Negativos, positivos y sospechosos por departamento fueron los siguientes: % de hatos N., Managua 80,76. % de hatos P. 9.62, % de hatos S. 3.91, Leon % de hatos N. 100.00, % de hatos P. 9.62, % de hatos S. 0, Granada % de hatos N. 86.66, % de Hatos P. 0, % de hatos S. 0, Rivas % de hatos N. 46.15, % de hatos P. 53.85, % de hatos S. 0. No se hace mención de los porcentajes de los departamentos de Masaya, Carazo y Boaco, debido a los pocos hatos examinados en ellos. 3). El porcentaje de vacas en producción del total de vacas adultas es de 54.10% en la cuenca lechera y la zona del pacifico y el 54% en los hatos examinados. 4). La cantidad de leche para la venta es de 3.22 litros por vaca.

Static equilibrium of horizontal ring prominence

In 1980 the Beijing Observatory had successively observed sevesal rare completely closed ring prominences whose ring plane was approximately parallel to the solar surface with a characteristic life about 1—2 days. In this paper we discuss the static equilibrium of this kind of horizontal ring plasma under the simultaneous actions of magnetic force, gravity and pressure gradients. Assuming ring plasma with axisymmetry and rectangular plasma cross-section and adopting closed magnetic field boundary condition from the basic equations we obtain the exact zero order general solutions for magnetic field (force-free field) and density (pressure). We further obtain an eigen-solution for the zero order magnetic field and density as well as the first order magnetic field, thus giving a kind of the possible distribution of magnetic field and density for the horizontal closed ring prominence. The closed magnetic structure of ring prominence as presented in this paper, has no link with the force lines of the outside corona magnetic field. This is helpful to explain the great temperature difference between prominenee and corona.

Full-duplex wireless-over-fibre transmission incorporating a CWDM ring architecture with remote millimetre-wave LO delivery using a bi-directional SOA

We demonstrate the first full-duplex wireless-over-fibre transmission between a central station and a CWDM ring architecture with remote 40 GHz LO delivery using a bi-directional semiconductor optical amplifier. © 2005 Optical Society of America.

Ring-opening metathesis of bulky norbornene monomers and the radical-mediated hydrophosphonation of olefins

This thesis discusses two major topics: the ring-opening metathesis polymerization (ROMP) of bulky monomers and the radical-mediated hydrophosphonation of olefins. The research into the ROMP of bulky monomers is further divided into three chapters: wedge-shaped monomers, the alternating copolymerization of 1-methyloxanorbornene derivatives with cyclooctene, and the kinetic resolution polymerization of 1-methyloxanorbornene derivatives. The wedge-shaped monomers can be polymerized into diblock copolymers that possess photonic crystal properties. The alternating copolymerization of 1-methyloxanorbornene derivatives with cyclooctene is performed with > 90% alternation via two different routes: typical alternating copolymerization and a sequence editing approach. The kinetic resolution polymerization of these same 1-methyloxanorbornene monomers achieves only modest selectivity (S=4), but there is evidence that the growing polymer chain forms a helix that influences the selectivity of the resolution. The last topic is the radical-mediated hydrophosphonation of olefins. This synthetic method provides access to Wittig reagents that are capable of highly cis-selective olefinations of aldehydes.

Aqueous ring-opening metathesis polymerizations

Past workers in this group as well as in others have made considerable progress in the understanding and development of the ring-opening metathesis polymerization (ROMP) technique. Through these efforts, ROMP chemistry has become something of an organometallic success story. Extensive work was devoted to trying to identify the catalytically active species in classical reaction mixtures of early metal halides and alkyl aluminum compounds. Through this work, a mechanism involving the interconversion of metal carbenes and metallacyclobutanes was proposed. This preliminary work finally led to the isolation and characterization of stable metal carbene and metallacyclobutane complexes. As anticipated, these well-characterized complexes were shown to be active catalysts. In a select number of cases, these catalysts have been shown to catalyze the living polymerization of strained rings such as norbornene. The synthetic control offered by these living systems places them in a unique category of metal catalyzed reactions. To take full advantage of these new catalysts, two approaches should be explored. The first takes advantage of the unusual fact that all of the unsaturation present in the monomer is conserved in the polymer product. This makes ROMP techniques ideal for the synthesis of highly unsaturated, and fully conjugated polymers, which find uses in a variety of applications. This area is currently under intense investigation. The second aspect, which should lend itself to fruitful investigations, is expanding the utility of these catalysts through the living polymerization of monomers containing interesting functional groups. Polymer properties can be dramatically altered by the incorporation of functional groups. It is this latter aspect which will be addressed in this work.

After a general introduction to both the ring-opening metathesis reaction (Chapter 1) and the polymerization of fuctionalized monomers by transition metal catalysts (Chapter 2), the limits of the existing living ROMP catalysts with functionalized monomers are examined in Chapter 3. Because of the stringent limitations of these early metal catalysts, efforts were focused on catalysts based on ruthenium complexes. Although not living, and displaying unusually long induction periods, these catalysts show high promise for future investigations directed at the development of catalysts for the living polymerization of functionalized monomers. In an attempt to develop useful catalysts based on these ruthenium complexes, efforts to increase their initiation rates are presented in Chapter 4. This work eventually led to the discovery that these catalysts are highly active in aqueous solution, providing the opportunity to develop aqueous emulsion ROMP systems. Recycling the aqueous catalysts led to the discovery that the ruthenium complexes become more activated with use. Investigations of these recycled solutions uncovered new ruthenium-olefin complexes, which are implicated in the activation process. Although our original goal of developing living ROMP catalysts for the polymerization of fuctionalized monomers is yet to be realized, it is hoped that this work provides a foundation from which future investigations can be launched.

In the last chapter, the ionophoric properties of the poly(7-oxanobornene) materials is briefly discussed. Their limited use as acyclic host polymers led to investigations into the fabrication of ion-permeable membranes fashioned from these materials.