Ajit Mal

Abstract: We have developed a transparent organic polymeric material that can repeatedly mend or "re-mend" itself under mild conditions. The material is a tough solid at room temperature and below with mechanical properties equaling those of commercial epoxy resins. At temperatures above 120 degrees C, approximately 30% (as determined by solid-state nuclear magnetic resonance spectroscopy) of "intermonomer" linkages disconnect but then reconnect upon cooling, This process is fully reversible and can be used to restore a fractured part of the polymer multiple times, and it does not require additional ingredients such as a catalyst, additional monomer, or special surface treatment of the fractured interface.

Abstract: Two new remendable highly cross-linked polymers, 2ME4F and 2MEP4F, were prepared without solvent. Solid-state NMR (nuclear magnetic resonance) was used to study the thermal reversibility of Diels−Alder (DA) cross-linking, and it was found that DA connections and disconnections of both polymers are thermally reversible. Differential scanning calorimeter and dynamical mechanical analysis were applied to study thermal and mechanical properties of these materials, and it is found that the glass transition temperature (Tg) of 2ME4F is about 30−40 °C and that of 2MEP4F is about 80 °C. A qualitative study of the healing efficiency of 2MEP4F showed that cracks can be healed effectively with a simple thermal healing procedure. This process can be repeated to heal cracks multiple times.

Abstract: A matrix method is presented for the solution of wave propagation problems in multilayered anisotropic media subjected to time harmonic disturbances. The method is applied to obtain the formal solution of the response of layered composite plates to time harmonic and spatially periodic surface loads. It is shown that the solution leads to stable numerical schemes for the evaluation of the displacement and stress fields within the laminate. Numerical results for specific problems will be presented in a separate paper.

Abstract: A review of the elementary theory of elasticity Cartesian tensors kinematics of deformation balance laws and analysis of stress constitutive equations elastostatics solution of linear elastostatic problems by special technique linear elastodynamics.

Abstract: Three parallel algorithms for classical molecular dynamics are presented. The first assigns each processor a fixed subset of atoms; the second assigns each a fixed subset of inter-atomic forces to compute; the third assigns each a fixed spatial region. The algorithms are suitable for molecular dynamics models which can be difficult to parallelize efficiently—those with short-range forces where the neighbors of each atom change rapidly. They can be implemented on any distributed-memory parallel machine which allows for message-passing of data between independently executing processors. The algorithms are tested on a standard Lennard-Jones benchmark problem for system sizes ranging from 500 to 100,000,000 atoms on several parallel supercomputers--the nCUBE 2, Intel iPSC/860 and Paragon, and Cray T3D. Comparing the results to the fastest reported vectorized Cray Y-MP and C90 algorithm shows that the current generation of parallel machines is competitive with conventional vector supercomputers even for small problems. For large problems, the spatial algorithm achieves parallel efficiencies of 90% and a 1840-node Intel Paragon performs up to 165 faster than a single Cray C9O processor. Trade-offs between the three algorithms and guidelines for adapting them to more complex molecular dynamics simulations are also discussed.

Abstract: This introduction begins with a brief history of SHM technology development. Recent research has begun to recognise that a productive approach to the Structural Health Monitoring (SHM) problem is to regard it as one of statistical pattern recognition (SPR); a paradigm addressing the problem in such a way is described in detail herein as it forms the basis for the organisation of this book. In the process of providing the historical overview and summarising the SPR paradigm, the subsequent chapters in this book are cited in an effort to show how they fit into this overview of SHM. In the conclusions are stated a number of technical challenges that the authors believe must be addressed if SHM is to gain wider acceptance.

Abstract: Human skin is a remarkable organ. It consists of an integrated, stretchable network of sensors that relay information about tactile and thermal stimuli to the brain, allowing us to maneuver within our environment safely and effectively. Interest in large-area networks of electronic devices inspired by human skin is motivated by the promise of creating autonomous intelligent robots and biomimetic prosthetics, among other applications. The development of electronic networks comprised of flexible, stretchable, and robust devices that are compatible with large-area implementation and integrated with multiple functionalities is a testament to the progress in developing an electronic skin (e-skin) akin to human skin. E-skins are already capable of providing augmented performance over their organic counterpart, both in superior spatial resolution and thermal sensitivity. They could be further improved through the incorporation of additional functionalities (e.g., chemical and biological sensing) and desired properties (e.g., biodegradability and self-powering). Continued rapid progress in this area is promising for the development of a fully integrated e-skin in the near future.

Abstract: The controlled synthesis of monodisperse nanospheres faces a number of difficulties, such as extensive crosslinking during hydrothermal processes. Here, the authors show a route for the controlled synthesis of mesoporous polymer nanospheres, which can be further converted into carbon nanospheres through carbonization.

Abstract: Smart materials with an in-built ability to repair damage caused by normal wear and tear could prove useful in a wide range of applications. Most healable polymer-based materials so far developed require heating of the damaged area. But Burnworth et al. have now produced materials — in the form of polymer strands linked through metal complexes — that can be mended through exposure to light. The metal complexes in these materials can absorb ultraviolet light that is then converted into heat, which temporarily unlinks the polymer strands for quick and efficient defect healing. In principle, healing can take place in situ and while under load. Polymers with the ability to repair themselves after sustaining damage could extend the lifetimes of materials used in many applications1. Most approaches to healable materials require heating the damaged area2,3,4. Here we present metallosupramolecular polymers that can be mended through exposure to light. They consist of telechelic, rubbery, low-molecular-mass polymers with ligand end groups that are non-covalently linked through metal-ion binding. On exposure to ultraviolet light, the metal–ligand motifs are electronically excited and the absorbed energy is converted into heat. This causes temporary disengagement of the metal–ligand motifs and a concomitant reversible decrease in the polymers’ molecular mass and viscosity5, thereby allowing quick and efficient defect healing. Light can be applied locally to a damage site, so objects can in principle be healed under load. We anticipate that this approach to healable materials, based on supramolecular polymers and a light–heat conversion step, can be applied to a wide range of supramolecular materials that use different chemistries.