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171,292 result(s) for "Materials Design."
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Materials for design
Over the last ten years there has been a huge growth in the area of materials for design, but most books on this subject deal with advanced, semi-formed materials (that is, materials sold as sheet, rod, tube, etc.). This book provides much-needed information on the raw materials, and the low-down on how these can be used.
Graphene and Iron Reinforced Polymer Composite Electromagnetic Shielding Applications: A Review
With advancements in the automated industry, electromagnetic inferences (EMI) have been increasing over time, causing major distress among the end-users and affecting electronic appliances. The issue is not new and major work has been done, but unfortunately, the issue has not been fully eliminated. Therefore, this review intends to evaluate the previous carried-out studies on electromagnetic shielding materials with the combination of Graphene@Iron, Graphene@Polymer, Iron@Polymer and Graphene@Iron@Polymer composites in X-band frequency range and above to deal with EMI. VOSviewer was also used to perform the keyword analysis which shows how the studies are interconnected. Based on the carried-out review it was observed that the most preferable materials to deal with EMI are polymer-based composites which showed remarkable results. It is because the polymers are flexible and provide better bonding with other materials. Polydimethylsiloxane (PDMS), polyaniline (PANI), polymethyl methacrylate (PMMA) and polyvinylidene fluoride (PVDF) are effective in the X-band frequency range, and PDMS, epoxy, PVDF and PANI provide good shielding effectiveness above the X-band frequency range. However, still, many new combinations need to be examined as mostly the shielding effectiveness was achieved within the X-band frequency range where much work is required in the higher frequency range.
Material thoughts
This work explores the thinking of leading designers and producers that are able to challenge convention through curiosity and experimentation. It aims to promote a physical enquiry of materials and a mentality to constantly ask what could be done 'if' rather than to consider only what is being done.
Metavalent or Hypervalent Bonding: Is There a Chance for Reconciliation?
A family of solids including crystalline phase change materials such as GeTe and Sb2Te3, topological insulators like Bi2Se3, and halide perovskites such as CsPbI3 possesses an unconventional property portfolio that seems incompatible with ionic, metallic, or covalent bonding. Instead, evidence is found for a bonding mechanism characterized by half‐filled p‐bands and a competition between electron localization and delocalization. Different bonding concepts have recently been suggested based on quantum chemical bonding descriptors which either define the bonds in these solids as electron‐deficient (metavalent) or electron‐rich (hypervalent). This disagreement raises concerns about the accuracy of quantum–chemical bonding descriptors is showed. Here independent of the approach chosen, electron‐deficient bonds govern the materials mentioned above is showed. A detailed analysis of bonding in electron‐rich XeF2 and electron‐deficient GeTe shows that in both cases p‐electrons govern bonding, while s‐electrons only play a minor role. Yet, the properties of the electron‐deficient crystals are very different from molecular crystals of electron‐rich XeF2 or electron‐deficient B2H6. The unique properties of phase change materials and related solids can be attributed to an extended system of half‐filled bonds, providing further arguments as to why a distinct nomenclature such as metavalent bonding is adequate and appropriate for these solids. Recently, the bonding in crystalline phase change materials has been disputed, with two opposing views emerging. The bonds are either described as electron‐deficient or electron‐rich. Here, a coherent view of bonding is presented comparing density‐ and orbital‐based quantum‐chemical techniques. Consistently, both describe phase change materials as electron‐deficient, i.e. metavalent solids with a remarkable and well‐defined set of properties.
Engineering materials : properties and selection
Encompassing all significant material systems-metals, ceramics, plastics, and composites, this text incorporates the most up-to-date information on material usage and availability, addresses the increasingly global nature of the field, and reflects the suggestions of numerous adopters of previous editions.
Recent Developments in Laser Welding of Aluminum Alloys to Steel
The development of high-performance dissimilar aluminum–steel joints is necessary to promote the feasibility of multi-material design and lightweight manufacturing. However, joining aluminum to steel is a challenging task mainly due to the formation of brittle intermetallic compounds (IMC) at the joint interface. Laser welding is considered a very promising joining process for dissimilar materials, although its application in industry is still limited by the insufficient mechanical performance of the joints. The present paper aims to give a comprehensive review of relevant recent research work on laser joining of aluminum to steel, contributing to highlighting the latest achievements that could boost acceptance of laser joining of dissimilar materials by the modern industries. To this end, the most important challenges in laser joining of aluminum to steel are presented, followed by recent approaches to overcome these challenges, the state-of-art of comprehension of IMC formation and growth, and the different strategies to minimize them.
Energy landscapes and functions of supramolecular systems
By means of two supramolecular systems—peptide amphiphiles engaged in hydrogen-bonded β-sheets, and chromophore amphiphiles driven to assemble by π -orbital overlaps—we show that the minima in the energy landscapes of supramolecular systems are defined by electrostatic repulsion and the ability of the dominant attractive forces to trap molecules in thermodynamically unfavourable configurations. These competing interactions can be selectively switched on and off, with the order of doing so determining the position of the final product in the energy landscape. Within the same energy landscape, the peptide-amphiphile system forms a thermodynamically favoured product characterized by long bundled fibres that promote biological cell adhesion and survival, and a metastable product characterized by short monodisperse fibres that interfere with adhesion and can lead to cell death. Our findings suggest that, in supramolecular systems, functions and energy landscapes are linked, superseding the more traditional connection between molecular design and function. The energy landscapes of supramolecular systems are linked to their functions, as demonstrated by the switching of the balance of competing interactions in self-assembling amphiphiles.
Mass to membrane
If we look at the historical evolution of architecture - from the massive pyramids of Egypt to the framed structures of Greek and Roman construction, to the lighter Gothic vaulting and eventually modern architecture of the twentieth century - we see a continuous, almost linear progression from solid mass construction to diaphanous skins of glass and steel.