Melilite Formation in a Samarium-Stabilized α-Sialon Ceramic during Postsintering Heat Treatments

The formation of the melilite solid solution phase (M'), Sm₂Si_3−xAl_xO_3+xN_4−x, in an α-sialon sample of overall composition Sm_0.6Si_9.28Al_2.69O_1.36N_14.76, was studied as a function of time in the temperature interval 1375–1525°C. The alpha-sialon ceramic contained only minor amounts of the 21R sialon polytype and some residual grain-boundary glass before heat treatment. In situ studies by high-temperature X-ray diffraction were combined with postsintering heat treatment followed by quenching. The M'-phase was found to be formed by two different mechanisms: either crystallization of the residual grain-boundary liquid or a direct decomposition of the α-sialon phase. The liquid crystallized during the first 10–15 min of heat treatment, yielding a rapid M'-phase formation, and further formation of M'-phase continued at a much slower rate, related to the decomposition of α-sialon.     

Radical copolymerization of higher alkyl methacrylates with acrylic esters and amides in toluene: influence of monomer association on copolymer composition

A strong concentration effect was found in a course of copolymerization of higher N-alkylacrylamides with higher alkyl acrylates in toluene, where the fraction of amide functions in copolymers obtained at low degrees of conversion decreases significantly with an increase in total concentration of monomers in solution. It was established that the observed effect is independent of the structure of alkyl substitutes for both types of monomers. The data gathered with the aid of IR spectroscopy and computer modeling show that this concentration effect relates to the formation of amide associates in solution. The concentration effect was absent for the copolymerization of higher alkyl methacrylates and higher alkyl acrylates.     

Enhanced light scattering in coatings templated with interfacially stabilized colloids

Controlling inter-pore distances enables tuning the color or whiteness of microvoid coatings. While pore spacings have been modified in limited area inverse opal films, little work has occurred studying the feasibility of controlling pore spacings and thus the appearance of scalable, spray-on, microvoid inorganic coatings. In this work we investigated using interfacially stabilized colloidal templates to increase pore spacing and thus enhance Mie scattering in porous silica films. Coatings were fabricated by forming monodisperse colloids with or without a polyvinylpyrrolidone (PVP) interfacial stabilizing layer, dispersing them in a silica precursor solution, and spraying this suspension on a substrate. The films were cured and the colloids subsequently solution extracted at mild temperatures to create porous surfaces. Coatings made with PVP coated colloids had thicker pore walls and scattered light approximately 3× more efficiently than coatings made with bare colloids. Furthermore, a viewing angle dependent color shift was observed in the PVP colloid templated coatings. Side illumination of the samples with white light causes an orange appearance under angles of specular reflection, while a light blue appearance is observed out of these angles because of strong Mie scattering of short-wavelength radiation in both situations. Lastly, modeling based on Mie scattering confirms that it is the dominant optical effect in these coatings and explains the appearance of these coatings. The approach of using interfacially stabilized colloids to improve pore separation applies to many porous films and should be considered when increased light scattering is desired.     

Emerging correlation optics

This feature issue of Applied Optics contains a series of selected papers reflecting the state-of-the-art of correlation optics and showing synergetics between the theoretical background and experimental techniques.