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Chapter 7 is a short chapter describing some methods to investigate the vibrational structure of materialsusing infrared radiation and extremely high resolution inelastic X-ray scattering.
Chapter 6 describes a range of methods to determine different aspects of the electronic structure of materials. These include both core level photoemission (and the associated 'chemical' shifts) and valence band photoemission, notably including angle-resolved photoelectron spectroscopy (ARPES). The use of X-ray absorption near-edge structures (XANES) and the related technique of X-ray magnetic circular dicroism (XMCD) using circularly-polarised radiation is also described, as is the use of X-ray emission spectroscopy (XES) and resonant inelastic X-ray scattering (RIXS) and Compton scattering. Finally, the use of photoemission and photoionisation to investigate gas-phase molecular structure is described.
Chapter 5 describes techniques to determine the localstructure of materials both on an atomic and microscopic scale that do not rely on X-ray crystal diffraction. These include small angle scattering (SAXS) and wide angle scattering (WAXS), near-edge and extended X-ray absorption fine structure spectroscopy (XAFS, NEXAFS, EXAFS) but also photoelectron diffraction and X-ray fluorescence holography.
Reliable hepatitis C prevalence estimates are crucial for a good follow-up of the indicators to eliminate hepatitis by 2030 as set by the World Health Organization. In Belgium, no recent national population-based hepatitis C virus (HCV) seroprevalence estimate is available. The current study estimated HCV prevalence as part of the first Belgian Health Examination Survey, which was organized in 2018 as a second stage of the sixth Belgian Health Interview Survey. This national population-based cross-sectional study resulted in a weighted national HCV seroprevalence of 0.02% (95% CI 0.00–0.07%). The results show a much lower HCV seroprevalence compared to previous studies.
The crystal structure of brigatinib Form A has been solved and refined using synchrotron X-ray powder diffraction data and optimized using density functional theory techniques. Brigatinib Form A crystallizes in space group P-1 (#2) with a = 9.59616(20), b = 10.9351(3), c = 14.9913(6) Å, α = 76.1210(13), β = 79.9082(11), γ = 74.0802(6)°, V = 1458.497(15) Å3, and Z = 2. Structure solution was complicated by the lowest cost factor solution having an unreasonable conformation of the dimethylphosphoryl group. The second-best structure yielded a better refinement. The crystal structure is characterized by alternating layers of aliphatic and aromatic portions of the molecules along the b-axis. Strong N–H⋯N hydrogen bonds link the molecules into pairs, with a graph set R2,2(8). There is a strong intramolecular N–H⋯O hydrogen bond to the phosphoryl group, which determines the orientation of this group. The powder pattern has been submitted to ICDD® for inclusion in the Powder Diffraction File™ (PDF®).
Learn about the properties of synchrotron radiation and its wide range of applications in physics, materials science and chemistry with this invaluable reference. This thorough text describes the physical principles of the subject, its source and methods of delivery to the sample, as well as the different techniques that use synchrotron radiation to analyse the electronic properties and structure of crystalline and non-crystalline materials and surfaces. Explains applications to study the structure and electronic properties of materials on a microscopic, nanoscopic and atomic scale. An excellent resource for current and future users of these facilities, showing how the available techniques can complement information obtained in users' home laboratories. Perfect for graduate and senior undergraduate students taking specialist courses in synchrotron radiation, in addition to new and established researchers in the field.
The crystal structure of ivermectin hemihydrate ethanolate has been solved and refined using synchrotron X-ray powder diffraction data and optimized using density functional techniques. Ivermectin hemihydrate ethanolate crystallizes in space group C2 (#5) with a = 40.9374(10), b = 9.26951(6), c = 14.9488(2) Å, β = 73.047(1)°, V = 5426.12(8) Å3, and Z = 4. The structure consists of layers of ivermectin molecules parallel to the bc-plane. The water and ethanol molecules reside in small voids in the structure. The water molecule, the ethanol molecule, and hydroxyl groups act as donors in O–H⋯O hydrogen bonds. Several C–H⋯O hydrogen bonds were detected. The powder pattern has been submitted to ICDD for inclusion in the Powder Diffraction File™.
This comprehensive textbook provides a modern, self-contained treatment for upper undergraduate and graduate level students. It emphasizes the links between structure, defects, bonding, and properties throughout, and provides an integrated treatment of a wide range of materials, including crystalline, amorphous, organic and nano- materials. Boxes on synthesis methods, characterization tools, and technological applications distil specific examples and support student understanding of materials and their design. The first six chapters cover the fundamentals of extended solids, while later chapters explore a specific property or class of material, building a coherent framework for students to master core concepts with confidence, and for instructors to easily tailor the coverage to fit their own single semester course. With mathematical details given only where they strengthen understanding, 400 original figures and over 330 problems for hands-on learning, this accessible textbook is ideal for courses in chemistry and materials science.
One important characteristic of all aerogels is their large specific surface area. Almost in every paper on aerogels, not only the envelope density is reported but also the specific surface area in terms of inner surface per unit mass. We first present some fundamental relations for the specific surface area of particulate aerogels, such as silica or RF aerogels, and fibrillar aerogels such as cellulose. We then define terms and present selected experimental results to compare the models with reality.Techniques to measure the surface area by nitrogen adsorption and the fundamental equations behind them such as the famous BET theory or the t-plot method are derived and compared with experimental results.
Numerous daily-life materials exhibit a porous structure, e.g., foams made from different polymers (polystyrene, polyurethane), clays, tiles, bricks, oxide ceramics, bones, sponges, wood or diatoms. In many cases, the mechanical properties can be described by simple scaling laws with the relative or envelope density being the decisive factor. It is generally agreed that similar scaling laws apply to aerogels and xerogels, but the special nanostructured nature of aerogels and the mode used to form them out of a solution of monomers or polymers make an essential difference. A brief discussion of the conventional approach for closed and open cell foams or honeycombs based on the famous book written by Lorna J.Gibson and Michael F. Ashby on porous materials is given and extended to aerogels. Beforewe discuss aerogels, we briefly give for newcomers in the field of mechanical properties some textbook knowledge about mechanical testing. The chapter deals then with elastic and plastic properties of aerogels, compares modelling with experimental results and discusses deviations from classical porous media theory observed in aerogels.
Lignin is a polyphenolic compound found in plant tissues, especially wood and bark. The lignin content determines the quality of wood biochar in agroecological uses, and is used in the production of synthetic resins and adhesives. Despite its importance in plant physiology and its agricultural and industrial utility, there exists a wide gap of knowledge of lignin contents of tropical hardwood trees of South Asia, except for a few species. We present here the first estimation of lignin content in wood and bark of 48 species from tropical deciduous forests of India. We show that some species are characterized by greater wood lignin (WL) compared with bark lignin (BL) content, contrary to the generalization held for hardwood trees, and suggest a plausible correspondence between the WL to BL ratio and timber quality.