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

Preceramic polymers were proposed over 30 years ago as precursors for the fabrication of mainly Si-based advanced ceramics, generally denoted as polymer-derived ceramics (PDCs). The polymer to ceramic transformation process enabled significant technological breakthroughs in ceramic science and technology, such as the development of ceramic fibers, coatings, or ceramics stable at ultrahigh temperatures (up to 2000°C) with respect to decomposition, crystallization, phase separation, and creep. In recent years, several important advances have been achieved such as the discovery of a variety of functional properties associated with PDCs. Moreover, novel insights into their structure at the nanoscale level have contributed to the fundamental understanding of the various useful and unique features of PDCs related to their high chemical durability or high creep resistance or semiconducting behavior. From the processing point of view, preceramic polymers have been used as reactive binders to produce technical ceramics, they have been manipulated to allow for the formation of ordered pores in the meso-range, they have been tested for joining advanced ceramic components, and have been processed into bulk or macroporous components. Consequently, possible fields of applications of PDCs have been extended significantly by the recent research and development activities. Several key engineering fields suitable for application of PDCs include high-temperature-resistant materials (energy materials, automotive, aerospace, etc.), hard materials, chemical engineering (catalyst support, food- and biotechnology, etc.), or functional materials in electrical engineering as well as in micro/nanoelectronics. The science and technological development of PDCs are highly interdisciplinary, at the forefront of micro- and nanoscience and technology, with expertise provided by chemists, physicists, mineralogists, and materials scientists, and engineers. Moreover, several specialized industries have already commercialized components based on PDCs, and the production and availability of the precursors used has dramatically increased over the past few years. In this feature article, we highlight the following scientific issues related to advanced PDCs research: (1) General synthesis procedures to produce silicon-based preceramic polymers.
(2) Special microstructural features of PDCs.
(3) Unusual materials properties of PDCs, that are related to their unique nanosized microstructure that makes preceramic polymers of great and topical interest to researchers across a wide spectrum of disciplines.
(4) Processing strategies to fabricate ceramic components from preceramic polymers.
(5) Discussion and presentation of several examples of possible real-life applications that take advantage of the special characteristics of preceramic polymers. Note: In the past, a wide range of specialized international symposia have been devoted to PDCs, in particular organized by the American Ceramic Society, the European Materials Society, and the Materials Research Society. Most of the reviews available on PDCs are either not up to date or deal with only a subset of preceramic polymers and ceramics (e.g., silazanes to produce SiCN-based ceramics). Thus, this review is focused on a large number of novel data and developments, and contains materials from the literature but also from sources that are not widely available.

Polymer-Derived Ceramics: 40 Years of Research and Innovation in Advanced Ceramics

https://hal.archives-ouvertes.fr/hal-00120432/document

Raman Spectroscopy of Nanomaterials: How Spectra Relate to Disorder, Particle Size and Mechanical Properties

The extremely high melting point of many ceramics adds challenges to additive manufacturing as compared with metals and polymers. Because ceramics cannot be cast or machined easily, three-dimensional (3D) printing enables a big leap in geometrical flexibility. We report preceramic monomers that are cured with ultraviolet light in a stereolithography 3D printer or through a patterned mask, forming 3D polymer structures that can have complex shape and cellular architecture. These polymer structures can be pyrolyzed to a ceramic with uniform shrinkage and virtually no porosity. Silicon oxycarbide microlattice and honeycomb cellular materials fabricated with this approach exhibit higher strength than ceramic foams of similar density. Additive manufacturing of such materials is of interest for propulsion components, thermal protection systems, porous burners, microelectromechanical systems, and electronic device packaging.

Additive manufacturing of polymer-derived ceramics

Boron carbide is a strategic material, finding applications in nuclear industry, armour for personnel and vehicle safety, rocket propellant, etc. Its high hardness makes it suitable for grinding and cutting tools, ceramic bearing, wire drawing dies, etc. Boron carbide is commercially produced either by carbothermic reduction of boric acid in electric furnaces or by magnesiothermy in presence of carbon. Since many specialty applications of boron carbide require dense bodies, its densification is of great importance. Hot pressing and hot isostatic pressing are the main processes employed for densification. In the recent past, various researchers have made attempts to improve the existing methods and also invent new processes for synthesis and consolidation of boron carbide. All the techniques on synthesis and consolidation of boron carbide are discussed in detail and critically reviewed.

Synthesis and consolidation of boron carbide: a review

The oxygen free Si–C fibre (Hi-Nicalon) consists of β-SiC nanocrystals (≈5nm) and stacked carbon layers of 2–3nm in extension, in the form of carbon network along the fibre. This microstructure gives rise to a high density, tensile strength, stiffness and electrical conductivity. With respect to a Si–C–O fibre (Nicalon NL202), the Si–C fibres have a much greater thermal stability owing to the absence of the unstable SiOxCy phase. Despite its high chemical stability, it is nevertheless subject to a slight structural evolution at high temperatures of both SiC and free carbon phases, beginning at pyrolysis temperatures in the range 1200–1400°C and improving with increasing pyrolysis temperature and annealing time. A moderate superficial decomposition is also observed beyond 1400°C, in the form of a carbon enriched layer whose thickness increases as the pyrolysis temperature and annealing time are raised. The strength reduction at ambient for pyrolysis temperatures below 1600°C could be caused by SiC coarsening or superficial degradation. Si–C fibres have a good oxidation resistance up to 1400°C, due to the formation of a protective silica layer.

Thermal stability of a PCS-derived SiC fibre with a low oxygen content (Hi-Nicalon)

https://hal-insu.archives-ouvertes.fr/insu-00159174/document

Quantitative structural and textural assessment of laminar pyrocarbons through Raman spectroscopy, electron diffraction and few other techniques

A comparative study of the chemical composition and microstructure of Hi-Nicalon, Hi-Nicalon type S, Tyranno SA, Sylramic and Carborundum fibres has been conducted. This analysis has confirmed results already published but has also evidenced some original features. The Hi-Nicalon type S fibre has a near stoichiometric composition but it still contains some oxygen (≈1 at. %) and free carbon (≈2 at. %). The expected near stoichiometric composition of both the Tyranno SA and the Sylramic fibres is only effective near the edge region, while the core of the fibres contains some amount of free carbon (e.g., up to ≈14 at. % and ≈6 at. % respectively in large diameter fibres) as well as some residual oxygen (≈0.5 at. %). The composition of the Carborundum fibre is very close to stoichiometric SiC except rare and localised free carbon or B4C inclusions. The properties of the different fibres, some of them still beeing at a development stage, are discussed from a chemical and a phase composition point of view, on the basis of what is known about their respective preparation process.

Georges Chollon

Papers

Thermal stability of a PCS-derived SiC fibre with a low oxygen content (Hi-Nicalon)

Quantitative structural and textural assessment of laminar pyrocarbons through Raman spectroscopy, electron diffraction and few other techniques

Characterization of nearly stoichiometric SiC ceramic fibres

Chemical, microstructural and thermal analyses of a naphthalene-derived mesophase pitch

Regenerative laminar pyrocarbon