Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

Phd by thesis

Titanium Dioxide Nanomaterials: Synthesis, Properties, Modifications, and Applications

Monodisperse samples of silver nanocubes were synthesized in large quantities by reducing silver nitrate with ethylene glycol in the presence of poly(vinyl pyrrolidone) (PVP). These cubes were single crystals and were characterized by a slightly truncated shape bounded by {100}, {110}, and {111} facets. The presence of PVP and its molar ratio (in terms of repeating unit) relative to silver nitrate both played important roles in determining the geometric shape and size of the product. The silver cubes could serve as sacrificial templates to generate single-crystalline nanoboxes of gold: hollow polyhedra bounded by six {100} and eight {111} facets. Controlling the size, shape, and structure of metal nanoparticles is technologically important because of the strong correlation between these parameters and optical, electrical, and catalytic properties.

http://science.sciencemag.org/content/sci/298/5601/2176.full.pdf

Shape-Controlled Synthesis of Gold and Silver Nanoparticles

This review focuses on the synthesis, protection, functionalization, and application of magnetic nanoparticles, as well as the magnetic properties of nanostructured systems. Substantial progress in the size and shape control of magnetic nanoparticles has been made by developing methods such as co-precipitation, thermal decomposition and/or reduction, micelle synthesis, and hydrothermal synthesis. A major challenge still is protection against corrosion, and therefore suitable protection strategies will be emphasized, for example, surfactant/polymer coating, silica coating and carbon coating of magnetic nanoparticles or embedding them in a matrix/support. Properly protected magnetic nanoparticles can be used as building blocks for the fabrication of various functional systems, and their application in catalysis and biotechnology will be briefly reviewed. Finally, some future trends and perspectives in these research areas will be outlined.

Magnetic nanoparticles: Synthesis, protection, functionalization, and application

3.2.3. Hydroformylation 2467 3.2.4. Dimerization 2468 3.2.5. Oxidative Cleavage and Ozonolysis 2469 3.2.6. Metathesis 2470 4. Terpenes 2472 4.1. Pinene 2472 4.1.1. Isomerization: R-Pinene 2472 4.1.2. Epoxidation of R-Pinene 2475 4.1.3. Isomerization of R-Pinene Oxide 2477 4.1.4. Hydration of R-Pinene: R-Terpineol 2478 4.1.5. Dehydroisomerization 2479 4.2. Limonene 2480 4.2.1. Isomerization 2480 4.2.2. Epoxidation: Limonene Oxide 2480 4.2.3. Isomerization of Limonene Oxide 2481 4.2.4. Dehydroisomerization of Limonene and Terpenes To Produce Cymene 2481

Chemical Routes for the Transformation of Biomass into Chemicals

Nanoengineering of a Magnetically Separable Hydrogenation Catalyst

Propene Polymerization with Silica-Supported Metallocene/MAO Catalysts.

Nanoscale palladium and nickel colloids prepared in the presence of certain tetra-n-octylammonium carboxylates contain a high proportion of nonequilibrium trigonal cross section particles. Specifically, those carboxylates which bear a hydroxy function at the α-position, e.g., tetra-n-octylammonium glycolate, exert a strong influence on the shape of the metal colloids. It is shown by an in situ FTIR study of the preparation of colloidal nickel from bis(cyclooctadiene)nickel in the presence of tetra-n-octylammonium glycolate that the interaction of the α-hydroxy carboxylate with the surface of the colloidal metal particle is likely to be the morphology-determining factor in the shape-selective preparation of these metal particles.

Surface Spectroscopic Study of the Stabilization Mechanism for Shape-Selectively Synthesized Nanostructured Transition Metal Colloids

We report here a detailed study on the surface topology of well-known ordered mesoporous silica (SBA-15, MCM-41, and KIT-6) and a series of nanocast Co3O4, Co3O4/CoFe2O4 composites by high resolution scanning electron microscopy (HR-SEM). Images of the MCM-41 structure were obtained at a resolution of the pore size, as well as a real space image of the gyroid silica surface of KIT-6 for two different aging temperatures, clearly revealing the differences of the aging procedures. By using the low voltage HR-SEM technique with extremely high resolution, we could very clearly show the influence of the template properties on the structure of the nanocast metal oxides.

Direct Imaging of Surface Topology and Pore System of Ordered Mesoporous Silica (MCM-41, SBA-15, and KIT-6) and Nanocast Metal Oxides by High Resolution Scanning Electron Microscopy

The replication of nanoscale structures by a direct templating process has been used in recent years in several creative ways for the synthesis of carbon replicas of zeolites[1] or ordered mesoporous carbons, such as CMK-1[2] or SNU-1.[3] Such processes rely on the fact that an ordered pore system, provided by the zeolite or ordered mesoporous silica, can be filled with a carbon precursor which is pyrolyzed and the silica leached with NaOH or HF solution. However, the technique is difficult to apply to the synthesis of framework compositions other than carbon, since the leaching of the silica typically also affects the material which is filled into the silica pore system. This problem could possibly be circumvented by not using the silica as the mold, but to instead go one step further and use the mesoporous ordered carbons as templates, which could then easily be removed by combustion or other techniques, as suggested recently.[4] On the macroscale, that is, for the production of photonic crystals, similar approaches are well known, where latex spheres are used as templates which can be removed by calcinations.[5] Also carbon black has been used as a TMtemplate∫, for instance to synthesize mesoporous zeolite single crystals, in which the pores, however, are disordered.[6] In a first attempt to show the feasibility of using ordered mesoporous carbon to synthesize ordered mesoporous oxides, we decided to template mesostructured silica by using an ordered mesoporous carbon. Although this brings one only back to the starting point, that is, a mesoporous silica, it COMMUNICATIONS

Bernd Tesche

Papers

Nanoengineering of a Magnetically Separable Hydrogenation Catalyst

Propene Polymerization with Silica-Supported Metallocene/MAO Catalysts.

Surface Spectroscopic Study of the Stabilization Mechanism for Shape-Selectively Synthesized Nanostructured Transition Metal Colloids

Direct Imaging of Surface Topology and Pore System of Ordered Mesoporous Silica (MCM-41, SBA-15, and KIT-6) and Nanocast Metal Oxides by High Resolution Scanning Electron Microscopy

Taking Nanocasting One Step Further: Replicating CMK‐3 as a Silica Material