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Biomaterials are being investigated to produce platform as scaffolds for cell/tissue growth and differentiation/regeneration. Cell-materials, chemical and biological interactions enable the application of more functional materials in the area of bioengineering, providing a pathway to novel treatment of humans suffering from tissue/organ damage and facing limitation of donation organs. Many studies were done on the tissue/organ regeneration. Development of new scaffolds for cell/tissue regeneration is a key R&D field. This chapter focuses on describing R&D on the novel ultrananocrystalline diamond (UNCD) film as a unique biomaterial for scaffolds for developmental biology. Recent research showed that cells grown on the surface of UNCD-coated culture dishes are similar to cell culture dishes with little retardation, indicating UNCD films have no or little inhibition on cell proliferation and are potentially appealing as substrate/scaffold materials. The mechanisms of cell adhesion on UNCD surfaces are proposed based on the experimental results. The comparisons of cell cultures on diamond-powder-seeded culture dishes and on UNCD-coated dishes with matrix-assisted laser desorption/ionization - time-of-flight mass spectroscopy (MALDI-TOF MS) and X-ray photoelectron spectroscopy (XPS) analyses provided valuable data to support the mechanisms proposed to explain the adhesion and proliferation of cells on the surface of UNCD scaffolds.
This chapter focuses on describing the work done to develop UNCD films as hermetic, bio-inert/biocompatible (made of C atoms-element of life in human DNA) coatings for encapsulation of Si-based microchips implantable inside the eye on the human retina, as the main component of an artificial retina to restore partial vision to people blinded by genetically-induced degeneration of the retina photoreceptors. The UNCD coating enables implantation of the Si microchips inside the eye, since diamond is totally inert to chemical attack by the eye humor, as opposed to Si, which is chemically etched. The chapter describes the synthesis of the UNCD films with focus on using a novel low temperature (≤ 400 ˚C) UNCD growth process to make it compatible with encapsulation of the Si microchip without destroying the CMOS transistors, in the chip, which exhibit a thermal budget of 400 ˚C, i.e., they cannot be heated beyond those temperatures since they would be destroyed. The chapter also the extremely smooth and dense surface needed for the UNCD coating to be hermetic.
This chapter describes the fundamental and applied science underlying the synthesis of UNCD films, using microwave plasma chemical vapor deposition (MOCVD) and hot filament chemical vapor deposition (HFCVD), and systematic characterization of the mechanical (hardness), tribological (coefficient of friction and surface resistance to wear), chemical (resistance to chemical attach by corrosive liquids and other environments, including body fluids), electrical, and biocompatibility properties of the UNCD films, which make UNCD coatings a multifunctional material for a new generation of external and implantable medical devices and prostheses with order of magnitude superior performance than current metals and polymers used in current medical devices and prostheses.
Retinal detachment is the separation of the sensory retinal tissue from the underlying pigmented epithelium, resulting in partial or total loss of human vision. Worldwide, 1:10,000 people per year suffer retina’s detachment. Current treatments include: 1) repositioning the sensory retina onto the rest of the retinal tissue, sealing the gap via laser heating or external freezing treatment. Current therapies for retina’s reattachment include using a silicone ring or a gas bubble to push the retina back into place. These modalities suffer from drawbacks such as choroidal detachment when using the silicone ring, or postoperative positioning of the patient. These techniques are not optimal for treating retinal detachment in the lower part of the eye. Thus, this chapter describes R&D that demonstrated a revolutionary method for retina reattachment, using a solution containing iron oxide super-paramagnetic nanoparticles (FDA approved) injected in the vitreous space of a rabbit eye and a rare earth magnet implanted on the sclera region outside the eye. Superparamagnetic particles, magnetic only when exposed to a magnetic field, are attracted to the magnet area pushing the retina back into place, then dissolve when the magnet is extracted.The magnet is coated with a biocompatible Ultrananocrystalline Diamond (UNCD) coating.
Pure titanium/titanium alloys are used in orthopedic and dental implants because of previously identified mechanical properties and biocompatibility. However, recent work shoed that these materials suffer from electrochemical corrosion when implanted in the body or the mouth, releasing metallic-oxide particles from oxidized surface, promoting inflammation around the implant, and implant failure. The novel UNCD coating discussed throughout this book exhibits excellent biocompatible and strong resistance to chemical attach by body fluids. This chapter describes the R&D performed to develop UNCD-coated commercial dental implants, hips and knees. The UNCD coating acts as a protective barrier between the implant and the biological environment, preventing release of metallic-oxide particles into the body. Research focused on investigating the osteointegration rate of titanium, UNCD-coated titanium, and UNCD/W-coated titanium implants, using the rat diaphyseal tibia as a model. Optical and SEM pictures showed superior osseointegration and resistance to chemical attach from body fluids, for UNCD-coated metal dental implantsover uncoated ones,
A comprehensive guide to the science of a transformational ultrananocrystalline-diamond (UNCDTM) thin film technology enabling a new generation of high-tech and external and implantable medical devices. Edited and co-authored by a co-originator and pioneer in the field, it describes the synthesis and material properties of UNCDTM coatings and multifunctional oxide/nitride thin films and nanoparticles, and how these technologies can be integrated into the development of implantable and external medical devices and treatments of human biological conditions. Bringing together contributions from experts around the world, it covers a range of clinical applications, including ocular implants, glaucoma treatment devices, implantable prostheses, scaffolds for stem cell growth and differentiation, Li-ion batteries for defibrillators and pacemakers, and drug delivery and sensor devices. Technology transfer and regulatory issues are also covered. This is essential reading for researchers, engineers and practitioners in the field of high-tech and medical device technologies across materials science and biomedical engineering.
Biological materials have been used in construction for as long as we have used wood and limestone; however, biotechnologies seem to offer the potential to grow materials to our specifications and even to allow complex structures to be self-assembled through biological processes. Several promising materials have been identified, including microbially induced calcium carbonate as a cement or mycelium grown on waste materials, which has potential as a structural or insulation material. These developments run parallel to a speculative design discourse – in which features future cities are grown, kept living and self-adapt – as well as research into engineered living materials (ELMs), at the cutting edge of material science and synthetic biology research into ELMs. This question invites a wide range of research contributions in which we identify, evaluate and speculate on the role that grown materials and structures will have on the future of construction. We invite not only experimental work on the latest method in this area but also critique and reflection beyond the ‘hype’ of these, potentially transformative, technologies and approaches.
The crystal structure of fulvestrant hydrate (ethyl acetate) has been solved and refined using synchrotron X-ray powder diffraction data, and optimized using density functional theory techniques. This solvate of fulvestrant crystallizes in space group R3 (#146) with a = 23.39188(16), c = 16.50885(13) Å, V = 7823.08(7) Å3, and Z = 9. The crystal structure is composed of triangular hydrogen-bonded chains of molecules around one of the threefold axes. The fluorinated ends of the molecules cluster around another threefold axis. Voids around a threefold axis occupy 8.1% of the unit cell volume, and are partially occupied by the water and ethyl acetate molecules. Both hydroxyl groups act as donors in O–H⋯O hydrogen bonds. These H-bonds form a large ring. The powder pattern has been submitted to ICDD® for inclusion in the Powder Diffraction File™ (PDF®).
The application of energy storage within transmission and distribution grids as non-wire alternative solutions (NWS) is hindered by the lack of readily available analysis tools, standardized planning processes, and practical know-how. This Element provides a theoretical basis along with examples and real-world case studies to guide grid planners in the siting, sizing, and lifetime techno-economic evaluation of storage systems. Many applications are illustrated including feeder peak shaving, feeder reliability improvements, transmission reliability, transmission congestion relief, and renewable integration. Three case studies, based on the author's consulting experience, illustrate the versatility of the analysis methods and provide a guide to grid planners while tackling real world problems.
Energy storage systems (ESS) exist in a wide variety of sizes, shapes and technologies. An energy storage system's technology, i.e. the fundamental energy storage mechanism, naturally affects its important characteristics including cost, safety, performance, reliability, and longevity. However, while the underlying technology is important, a successful energy storage project relies on a thorough and thoughtful implementation of the technology to meet the project's goals. A successful implementation depends on how well the energy storage system is architected and assembled. The system's architecture can determine its performance and reliability, in concert with or even despite the technology it employs. It is possible for an energy storage system with a good storage technology to perform poorly when implemented with a suboptimal architecture, while other energy storage systems with mediocre storage technologies can perform well when implemented with superior architectures.
In order to improve the resiliency of the grid and to enable integration of renewable energy sources into the grid, the utilization of battery systems to store energy for later demand is of the utmost importance. The implementation of grid-scale electrical energy storage systems can aid in peak shaving and load leveling, voltage and frequency regulation, as well as emergency power supply. Although the predominant battery chemistry currently used is Li-ion; due to cost, safety and sourcing concerns, incorporation of other battery technologies is of interest for expanding the breadth and depth of battery storage system installations. This Element discusses existing technologies beyond Li-ion battery storage chemistries that have seen grid-scale deployment, as well as several other promising battery technologies, and analyzes their chemistry mechanisms, battery construction and design, and corresponding advantages and disadvantages.
The structure, powder diffraction patterns and bandgap measurements of a series of manganese- and tungsten-containing alkaline-earth double perovskites (CaxSr2−x)MnWO6 (x = 0.25, 0.5, 0.75, 1.5, 1.75) have been investigated. Powder X-ray diffraction patterns of this series of compounds measured at room temperature have been submitted to be included in the Powder Diffraction File (PDF). These compounds crystallize in monoclinic space group P21/n (No.14). From (Ca1.75 Sr0.25)MnWO6 to (Ca0.25Sr1.75)MnWO6, lattice parameters a range from 5.6729(2) Å to 5.6774(4) Å, b from 5.5160(2) Å to 5.6638(4) Å, c from 7.8741(3) Å to 8.0051(4) Å, V from 240.39(2) Å3 to 257.410(12) Å3, and Z = 2. These compounds are pseudo-tetragonal. They all consist of distorted MnO6 and WO6 octahedra with rotational mismatch angles and tilt angles with respect to each other. For (CaxSr2−x)MnWO6, as x increases, the mismatch angles for MnO6 octahedra increase from 7.96 (6)° to 13.12(8)° and from 9.28(7)° to 14.87(9)° for WO6 octahedra. Correspondingly, the tilt angles range from 11.60(15)° to 14.20(3)° for MnO6, and from 13.34(2)° to 16.35(3)° for WO6. Bandgap measurements suggest that these compounds to be direct-allowed semiconductors with bandgaps ranging from 1.5 to 2.5 eV, indicating that members of (CaxSr2−x)MnWO6 are potential photocatalysts and photovoltaic materials that absorb visible light of the solar spectrum.
The crystal structure of merimepodib has been solved and refined using synchrotron X-ray powder diffraction data and optimized using density functional theory techniques. Merimepodib crystallizes in space group P212121 (#19) with a = 4.60827(3), b = 12.30400(14), c = 37.9583(4) Å, V = 2152.241(20) Å3, and Z = 4. The crystal structure is dominated by two chains of N–H⋯O hydrogen bonds along the a-axis. The solid-state conformation has a similar general shape to the minimum-energy conformation, but different orientations of several of the rings. The differences indicate that intermolecular interactions are important in determining the solid-state conformation. The powder pattern has been submitted to ICDD for inclusion in the Powder Diffraction File™ (PDF®).
The crystal structure of baricitinib has been solved and refined using synchrotron X-ray powder diffraction data and optimized using density functional techniques. Baricitinib crystallizes in space group I2/a (#15) with a = 11.81128(11), b = 7.06724(6), c = 42.5293(3) Å, β = 91.9280(4)°, V = 3548.05(5) Å3, and Z = 8. The crystal structure is characterized by hydrogen-bonded double layers parallel to the ab-planes. The dimers form a graph set R2,2(8). The sulfone ends of the molecules reside in the interlayer regions. The powder pattern has been submitted to ICDD for inclusion in the Powder Diffraction File™ (PDF®).
Corrosion is an important problem that engineers and scientists must overcome to avoid the collapse of structures, chemical processing plants, and metallic objects, which can lead to not only economic loss but also environmental and human losses. One of the simplest and most widely used methods to quantify corrosion rates (CRs) is the immersion test. The usual approach that has been used to date, to quantify the CR by this method, is to assume that the initial surface area of the corroding object remains constant over time. It is shown that such approximations underestimate the true CR and that they may lead to significant errors. A formula to calculate the CR considering changes in the area is presented in this work. The formula herein can be used to accurately quantify the CR by the immersion test and improve the quality of experimental data and the analysis and modeling of corrosion phenomena.
This chapter provides an overview of electromigration in metals, starting from the early studies on bulk metals to the current studies on copper interconnects. Asmicroelectronics technology advances, electromigration becomes an important reliability problem for on-chip interconnects, evolving from the microscale to the nanoscale in copper lines. Key concepts are introduced, including the electron wind force, the Blech short-length effects, and copper damascene interconnects.
In Chapter 8, the statistical nature of electromigration is described. Along with understanding of the basic physical degradation mechanisms, this is an important area of research due to the need for extrapolations from simple test structures to the product level. One has to keep in mind that electromigration testing is usually done on single-link structures. In some instances, a few links are stitched together in a series or parallel fashion, but massive-scale studies with large interconnect arrays have not been implemented yet as a standard testing methodology. Only the application of very large test structures with an extended amount of interconnect links encompassing metal lines and contacts/vias can lead to the detection of “early” or “extrinsic” failures, which are the limiting factor in the extrapolation to product-level interconnect systems. The detection of these early failures in electromigration and the complicated statistical nature of this important reliability phenomenon have been difficult issues to treat for decades in the past. In Chapter 8, an innovative technique utilizing large interconnect arrays in conjunction with the well-known Wheatstone Bridge are discussed, and both Al- and Cu-based interconnect technologies are described.