For dental implant treatment to be successful, esthetics, functionality, and cleanability are all required of the superstructure, the final prosthesis. Screw fixation and cementation have been the conventional methods of choice for the crown prosthesis of implants, but these individual methods cannot fulfill all the requirements. As a solution to this problem, we have devised a new implant superstructure restoration method (inlay covering esthetic technique) using computer-aided design / computer-aided manufacturing inlays. This involves the placement of an inlay covering the access hole in a highly translucent partially stabilized zirconia crown. This technique expands the indications for implant treatment and improves the oral quality of life of patients.

Non-natural mineralization of CaCO3 with special structures or morphology is generated during the crude oil migration, which is the main scale of alkaline/surfactant/polymer (ASP) flooding in oilfields, adversely affecting the oil recovery and causing environmental pollution. Up to now, the mineralization of superstructural symbiotic aragonites and the role of heavy alkyl-benzene sulfonate (HABS) in directing mineralization are still unclear. In this work, rosette-like, bouquet-like and dumbbell-like aragonite-based superstructure of symbiotic CaCO3 crystals were obtained in a simulated O/W emulsion with HABS, which can help understanding the diversified growth of CaCO3 scaling in oilfield. As a result, HABS stabilized micelles acted as a framework for mineralization, and promoted the accumulation of Ca2+ and CO32-, generating pre-nucleation clusters and partial ion pairs by electrostatic attraction. Following, the sequential nucleation of amorphous CaCO3 interconnected with HABS molecules. Finally, these nanoparticles transformed into micro-meter crystals via dissolution-reprecipitation, forming the superstructures that controlled by a synergistic effect between HABS and kerosene phase. This work may enrich the understanding of CaCO3 mineralization in oilfield, provide theoretical support for the prevention of hard carbonate scaling, and also provide a novel strategy for organic-inorganic composites manufacturing.

The evaluation of HAADF-STEM images of a sample with the composition Nb18W16O93 provided new insights in its real structure. The basic structure comprises an intact octahedral framework of the tetragonal tungsten bronze (TTB) type. The partial occupation of the pentagonal tunnels (PT) by metal-oxygen strings determines the oxygen to metal ratio (O/SM with M = Nb,W). For a large area, the O/SM was determined to be 2.755 which is smaller than the value of Nb18W16O93 which is O/SM = 2. 735. To a large extent, the threefold TTB superstructure structure of Nb8W9O47 with a high oxygen content is present (O/SM = 2.765). In addition, a new fourfold TTB superstructure was found in small domains: Nb12W11O63 with an O/SM = 2.739 obviously accommodates a part of the sample’s metal excess compared to the stable phase Nb8W9O47.

The formation of high-melting-point Cu₆Sn₅ interconnections is crucial to overcome the collapse of Sn-based micro-bumps and produce reliable intermetallic interconnections in three-dimensional (3D) package. However, because of the multiple reflows in 3D package manufacturing, Cu₆Sn₅ interconnections will experience the cyclic polymorphic transitions in the solid state. The repeated and abrupt change in the Cu₆Sn₅ lattice due to the cyclic polymorphic transitions can cause extreme strain oscillations, producing damages at the surface and in the interior of the Cu₆Sn₅ matrix. Moreover, because of the polymorphic-transition-induced grain splitting and superstructure phase formation, the reliability of Cu₆Sn₅ interconnections will thus face great challenges in 3D package. In addition, the Cu₆Sn₅ polymorphic transition is structure-dependent, and the η′↔η polymorphic transition will occur at the surface while the η′↔ηs↔η polymorphic transition will occur in the deep matrix. Our results can provide in-depth understandings of structural evolution and damage mechanism of Cu₆Sn₅ interconnections in real 3D package manufacturing.

Fuel gas network (FGN) synthesis is a systematic method for reducing fresh fuel consumption in a chemical plant. In this work, we address the synthesis of fuel gas network using block superstructure originally proposed for process design and intensification (Demirel et.al. [1]). Instead of a classical source-pool-sink superstructure, we consider a superstructure with multiple feed and product streams. These blocks interact with each other through direct flows that connect a block with its adjacent blocks and through jump flows that connect a block with all blocks. The blocks with feed streams are viewed as fuel sources and the blocks with product streams are regarded as fuel sinks. Addition blocks can be added as pools when there exists intermediate operations among 9 source blocks and sink blocks. These blocks can be arranged in a I × J two-dimensional grid with I = 1 for problems without pools, or I = 2 for problems with pools. J is determined by the maximum number of pools/sinks. With this representation, we formulate fuel gas network synthesis problem as a mixed-integer nonlinear (MINLP) problem to optimally design a fuel gas network with minimal total annul cost. We present a real-life case study from LNG plant to demonstrate the capability of the proposed approach.