ZSM-5 zeolite films on Si substrates grown by in situ seeding and secondary crystal growth and application in an electrochemical hydrocarbon gas sensor

ZSM-5 zeolite films were grown on Si substrates by a two-step hydrothermal synthesis consisting of in situ seeding and secondary crystal growth. The films were 8–13 μm thick and partly oriented with the c-axis perpendicular to the substrate surface. After ion exchange with sodium ions, one film was applied as solid electrolyte in a potentiometric hydrocarbon gas sensor. A fast and reversible voltage response of the sensor to varying propane concentrations (100 ppm – 10%) was observed in O₂/CO₂/N₂ gas mixtures at 723 K.     

Polymer-Derived SiOC/ZrO2 Ceramic Nanocomposites with Excellent High-Temperature Stability

Polymer-derived SiOC/ZrO₂ ceramic nanocomposites have been prepared using two synthetic approaches. A commercially available polymethylsilsesquioxane (MK Belsil PMS) was filled with nanocrystalline zirconia particles in the first approach. The second method involved the addition of zirconium tetra( n -propoxide), Zr(OⁿPr)₄, as zirconia precursor to polysilsesquioxane. The prepared materials have been subsequently cross-linked and pyrolyzed at 1100°C in argon atmosphere to provide SiOC/ZrO₂ ceramics. The obtained SiOC/ZrO₂ materials were characterized by means of X-ray diffraction, elemental analysis, Raman spectroscopy as well as transmission electron microscopy. Furthermore, annealing experiments at temperatures from 1300° to 1600°C have been performed. The annealing experiments revealed that the incorporation of ZrO₂ into the SiOC matrix remarkably increases the thermal stability of the composites with respect to crystallization and decomposition at temperatures exceeding 1300°C. The results obtained within this study emphasize the enormous potential of polymer-derived SiOC/ZrO₂ composites for high-temperature applications.     

Dense silicon carbonitride ceramics by pyrolysis of cross-linked and warm pressed polysilazane powders

This study reports on the pyrolysis and densifaction behavior of cross-linked poly(hydridomethylsilazane) powders. The influence of the cross-linking procedure such as temperature and annealing time of the polymer powders on the compaction behavior under cold and warm pressing conditions is discussed. The degree of cross-linking is determined by thermal mechanical analysis (TMA). In addition to particle sliding which is assumed to be the compaction mechanism obtained by cold-pressing, the polymer powder consolidates by plastic deformation applying warm-pressing. A continuous 3-dimensional polysilazane network is formed after a dwelling time under these conditions. Pyrolysis of the cross-linked and compacted polysilazane powder in argon at 1100°C gives crack-free amorphous silicon carbonitride Si_3+xC_x+yN₄ with compositions ranging from x=1·47 and y=0·88 for cold pressed samples to x=1·47 and y=1·86 for warm pressed materials. The residual open porosity is significantly reduced from 10–15 vol% in the cold pressed specimens to 1·3–5 vol% by the warm pressing procedure. The weight loss during pyrolysis between room temperature and 1300°C is about 5 wt% lower than that for cold pressed specimens. This result is explained by a reduced methane evolution during the polymer-to-ceramic conversion and is in accordance with the enhanced carbon content of the warm pressed material.     

A low-complexity low-spurs digital architecture for wideband PLL applications

This paper presents a non-ideality analysis of the wideband frequency synthesizer, and proposes a new digital architecture for signal modulation and quantization. Using error masking strategy, this method can offer smaller routing area and less power consumption without sacrificing any system performance. Simulation results confirm the theoretical predictions. Finally, the design guidelines are derived to fulfill the customized synthesizer specifications.     

Detecting landscape forms using Fourier transformation and singular value decomposition (SVD)

Landscape structure is a main determinant of ecological landscape potentials. The basic differentiation of relief into depressions and elevations at deliberately chosen scales can be managed comfortably by the Fourier transformation. The automated extraction of these structures from an elevation map using Fourier transformation or singular value decomposition can help to overcome complicated and errorprone procedures based on the determination of numerical structure parameters such as slope and aspect. The combination of automated extraction methods and moving window technology can lead to further, more integrated insights related to complex landscape patterns.     

Dissolution of Alumina, Sintering, and Crystallization in Glass Ceramic Composites for LTCC

Sintering and microstructure evolution of alkali-free calcium–alumo–borosilicate glass/α-Al₂O₃ composites (mean particle size ca. 2 μm) for low-temperature cofired ceramics were studied during heating at 5 K/min by heating microscopy, thermal analysis (DTA), X-ray diffraction (XRD), and electron microscopy (SEM). Composites fully densify at ≈830°C, not essentially influenced by the dissolution of alumina and glass crystallization. Thus wollastonite, as first crystalline phase, was detectable at 840°C. Above 900°C, a pronounced crystallization of anorthite is evident, reaching 60 wt% at 1050°C. Rietveld analyses of XRD data revealed that anorthite precipitates at the expenses of alumina, which declines from ≈33 to <10 wt%, and wollastonite, which fully declines from its maximum of ≈19 wt%. Based on XRD, we discuss the evolution of crystal mass fractions, the residual glass composition, the glass viscosity, and the effective shear viscosity of the composites under study during heating.