Case Reports of Enamel Microabrasion Associated with At-home Dental Bleaching After Orthodontic Bracket Removal

SUMMARY Adequate removal of residual bonded materials from the enamel surface after orthodontic bracket debonding is critical, since any remaining composite may compromise enamel surface morphology and esthetics. The following clinical case reports present the association of at-home dental bleaching using 10% carbamide peroxide and the removal of residual bonded material using a super fine, tapered diamond bur followed by the use of an enamel microabrasion product after orthodontic bracket debonding. The proposed treatment considerably improved the esthetics and successfully removed the grooves created during the removal of the bonding composite, resulting in a smooth enamel surface.

Roll Bonding Processes: State-of-the-Art and Future Perspectives

Roll bonding (RB) describes solid-state manufacturing processes where cold or hot rolling of plates or sheet metal is carried out for joining similar and dissimilar materials through the principle of severe plastic deformation. This review covers the mechanics of RB processes, identifies the key process parameters, and provides a detailed discussion on their scientific and/or engineering aspects, which influence the microstructure–mechanical behavior relations of processed materials. It further evaluates the available research focused on improving the metallurgical and mechanical behavior of bonded materials such as microstructure modification, strength enhancement, local mechanical properties, and corrosion and electrical resistance evolution. Moreover, current applications and advantages, limitations of the process and developments in dissimilar material hot roll bonding technologies for producing titanium to steel and stainless steel to carbon steel ultra-thick plates are also discussed. The paper concludes by deliberating on the bonding mechanisms, engineering guidelines and process–property–structure relationships, and recommending probable areas for future research.

Inorganic Salts of N-phenylbiguanidium(1+)—Novel Family with Promising Representatives for Nonlinear Optics

Seven inorganic salts containing N-phenylbiguanide as a prospective organic molecular carrier of nonlinear optical properties were prepared and studied within our research of novel hydrogen-bonded materials for nonlinear optics (NLO). All seven salts, namely N-phenylbiguanidium(1+) nitrate (C2/c), N-phenylbiguanidium(1+) perchlorate (P-1), N-phenylbiguanidium(1+) hydrogen carbonate (P21/c), bis(N-phenylbiguanidium(1+)) sulfate (C2), bis(N-phenylbiguanidium(1+)) hydrogen phosphate sesquihydrate (P-1), bis(N-phenylbiguanidium(1+)) phosphite (P21), and bis(N-phenylbiguanidium(1+)) phosphite dihydrate (P21/n), were characterised by X-ray diffraction (powder and single-crystal X-ray diffraction) and by vibrational spectroscopy (FTIR and Raman). Two salts with non-centrosymmetric crystal structures—bis(N-phenylbiguanidium(1+)) sulfate and bis(N-phenylbiguanidium(1+)) phosphite—were further studied to examine their linear and nonlinear optical properties using experimental and computational methods. As a highly SHG-efficient and phase-matchable material transparent down to 320 nm and thermally stable to 483 K, bis(N-phenylbiguanidium(1+)) sulfate is a promising novel candidate for NLO.

Non-conventional mineral binder-bonded lignocellulosic composite materials: A review

The construction industry suffers from unsustainability and contributes more than any other industrial sector to carbon emissions that lead to global warming. Increasing economic and environmental concerns related to conventional energy- and CO2-intensive building materials have propelled the rapid and sustained expansion of research in the area of plant-based inorganic mineral binder-bonded materials for the construction industry. The resulting composites can be qualified as eco-responsible, sustainable, and efficient multifunctional building materials. So far, most of these research efforts have not received as much attention as materials based on ordinary Portland cement (OPC). To address this gap, this review focuses on mineral binder-based lignocellulosic composites made from non-conventional inorganic mineral binders/ cements with low embodied energy and low carbon footprint, namely hydrated lime-based binders, magnesium-based cement, alkali-activated cement, and geopolymers, as sustainable alternatives to OPC-bonded lignocellulosic composites (state-of-the-art). The emphasis here is on the application potentials, the influence of production parameters on the material properties/ performance, and recent advancement in this field. Finally, a prediction is provided of future trends for these non-conventional mineral binder-bonded lignocellulosic composites.

Structure-Dependent Doppler Broadening Using a Generalized Thermal Scattering Law

The thermal scattering law (TSL), i.e., S(α,β), represents the momentum and energy exchange phase space for a material. The incoherent and coherent components of the TSL correlate an atom’s trajectory with itself and/or with other atoms in the lattice structure. This structural information is especially important for low energies where the wavelength of neutrons is on the order of the lattice interatomic spacing. Both thermal neutron scattering as well as low energy resonance broadening involve processes where incoming neutron responses are lattice dependent. Traditionally, Doppler broadening for absorption resonances approximates these interactions by assuming a Maxwell–Boltzmann distribution for the neutron velocity. For high energies and high temperatures, this approximation is reasonable. However, for low temperatures or low energies, the lattice structure binding effects will influence the velocity distribution. Using the TSL to determine the Doppler broadening directly introduces the material structure into the calculation to most accurately capture the momentum and energy space. Typically, the TSL is derived assuming cubic lattice symmetry. This approximation collapses the directional lattice information, including the polarization vectors and associated energies, into an energy-dependent function called the density of states. The cubic approximation, while valid for highly symmetric and uniformly bonded materials, is insufficient to capture the true structure. In this work, generalized formulation for the exact, lattice-dependent TSL is implemented within the Full Law Analysis Scattering System Hub (FLASSH) using polarization vectors and associated energies as fundamental input. These capabilities are utilized to perform the generalized structure Doppler broadening analysis for UO2.

Amidinium⋯carboxylate frameworks: predictable, robust, water-stable hydrogen bonded materials

This feature article describes the development of hydrogen bonded frameworks assembled using amidinium∙∙∙carboxylate hydrogen bonds, and discusses their structures, stabilities and applications.