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

https://www.researchgate.net/file.PostFileLoader.html?id=526892a1d4c118a61d4360bd&assetKey=AS%3A272155479085058%401441898330516

Porosity of 3D biomaterial scaffolds and osteogenesis.

Surface treatments of titanium dental implants for rapid osseointegration

Macroporous ceramics with pore sizes from 400 nm to 4 mm and porosity within the range 20%–97% have been produced for a number of well-established and emerging applications, such as molten metal filtration, catalysis, refractory insulation, and hot gas filtration. These applications take advantage of the unique properties achieved through the incorporation of macropores into solid ceramics. In this article, we review the main processing routes that can be used for the fabrication of macroporous ceramics with tailored microstructure and chemical composition. Emphasis is given to versatile and simple approaches that allow one to control the microstructural features that ultimately determine the properties of the macroporous material. Replica, sacrificial template, and direct foaming techniques are described and compared in terms of microstructures and mechanical properties that can be achieved. Finally, directions to future investigations on the processing of macroporous ceramics are proposed.

/pdf/processing-routes-to-macroporous-ceramics-a-review-1urld578zq.pdf

Processing Routes to Macroporous Ceramics: A Review

At present, strong requirements in orthopaedics are still to be met, both in bone and joint substitution and in the repair and regeneration of bone defects. In this framework, tremendous advances in the biomaterials field have been made in the last 50 years where materials intended for biomedical purposes have evolved through three different generations, namely first generation (bioinert materials), second generation (bioactive and biodegradable materials) and third generation (materials designed to stimulate specific responses at the molecular level). In this review, the evolution of different metals, ceramics and polymers most commonly used in orthopaedic applications is discussed, as well as the different approaches used to fulfil the challenges faced by this medical field.

https://royalsocietypublishing.org/doi/pdf/10.1098/rsif.2008.0151

Biomaterials in orthopaedics.

The substitution of between 0 and 1.6 wt% silicon (Si-HA) in hydroxyapatite (HA) inhibited densification at low temperatures (1000°–1150°C), with these effects being more significant as the level of silicon substitution was increased. For higher sintering temperatures (1200°–1300°C), the sintered densities of HA and Si-HA compositions were comparable. Examination of the ceramic microstructures by scanning electron microscopy (SEM) showed that silicon substitution also inhibited grain growth at higher sintering temperatures (1200°–1300°C). The negative effect of silicon substitution on the sintering of HA at low temperatures (1000°–1150°C) was reflected in the hardness values of the ceramics. However, for higher sintering temperatures, e.g., 1300°C, where sintered densities were comparable, the hardness values of Si-HA compositions were equal to or greater than that of HA, reflecting the smaller grain sizes observed for the former.

Effect of Silicon Substitution on the Sintering and Microstructure of Hydroxyapatite

The structural changes that occur during the transformation of a Ca-deficient apatite, prepared by a wet chemical method, to beta-TCP were investigated. X-ray diffraction (XRD) analysis of as-prepared samples and samples calcined at temperatures between 500 and 1100 degrees C showed that the transformation occurs over the temperature range 710-740 degrees C, under non-equilibrium conditions. The change in crystallite size with increasing calcination/sintering temperature was studied by XRD using the Scherrer formula. Fourier transform infra-red (FTIR) analysis indicated considerable structural change in samples above and below this temperature range. Changes were observed in the hydroxyl, carbonate and phosphate bands as the calcination temperature was increased from 500 to 1100 degrees C. Even once a single beta-TCP phase is obtained at 740 degrees C there remains a considerable amount of structural change at temperatures between 740 and 1100 degrees C. This effect was illustrated by an unusual change in the lattice parameters of the beta-TCP structure and significant changes in the phosphate bands of the FTIR spectra as the calcination temperature was increased. The results obtained in this study show that the combined experimental techniques of XRD and FTIR are excellent complimentary methods for characterizing structural changes that occur during phase transformations.

Characterization of the transformation from calcium-deficient apatite to beta-tricalcium phosphate.

The uptake of titanium ions by hydroxyapatite particles-structural changes and possible mechanisms

The sintering behaviour of a number of commercially produced 8 mol% yttria-stabilized zirconia powders has been studied. The effect of different sintering regimes on the density and microstructure of the sintered ceramic was determined using density measurements, scanning electron microscopy (SEM) and dilatometry. The chemical homogeneity, particle size and the morphology of the as-received powder were related to the sintering behaviour of the different commercial powders. Powders prepared via a route which involved a spray-drying step sintered more readily than those prepared without a spray-drying step. Plasma-derived powders did not sinter to as high an apparent density as co-precipitated powders. The effect of sample density on the ionic conductivity of sintered YSZ ceramics was studied using a.c. impedance spectroscopy. This technique allowed separation of the bulk and grain-boundary components, enabling clear intepretation of the effects of sample porosity of the conduction pathways. Ceramics prepared from the three different powders achieved a bulk ionic conductivity of ∼16 S cm-1 at 1000 °C for sintered densities of 95% or greater. The results obtained are compared to values reported for a variety of other commercial powders. © 1998 Kluwer Academic Publishers

Sinterability of commercial 8 mol% yttria-stabilized zirconia powders and the effect of sintered density on the ionic conductivity

The present study is aimed at investigating the contribution of two biologically important cations, Mg2+ and Sr2+, when substituted into the structure of hydroxyapatite (Ca10(PO4)6(OH)2,HA). The substituted samples were synthesized by an aqueous precipitation method that involved the addition of Mg2+- and Sr2+-containing precursors to partially replace Ca2+ ions in the apatite structure. Eight substituted HA samples with different concentrations of single (only Mg2+) or combined (Mg2+ and Sr2+) substitution of cations have been investigated and the results compared with those of pure HA. The obtained materials were characterized by X-ray powder diffraction, specific surface area and porosity measurements (N2 adsorption at 77 K), FT-IR and Raman spectroscopies and scanning electron microscopy. The results indicate that the co-substitution gives rise to the formation of HA and β-TCP structure types, with a variation of their cell parameters and of the crystallinity degree of HA with varying levels of substitution. An evaluation of the amount of substituents allows us to design and prepare BCP composite materials with a desired HA/β-TCP ratio.

Iain R. Gibson

Papers

Effect of Silicon Substitution on the Sintering and Microstructure of Hydroxyapatite

Characterization of the transformation from calcium-deficient apatite to beta-tricalcium phosphate.

The uptake of titanium ions by hydroxyapatite particles-structural changes and possible mechanisms

Sinterability of commercial 8 mol% yttria-stabilized zirconia powders and the effect of sintered density on the ionic conductivity

Magnesium- and strontium-co-substituted hydroxyapatite: the effects of doped-ions on the structure and chemico-physical properties