Microstructure compatibility

Haas-Santo, K., Eichtner, M., Schubert, K., Preparation of microstructure compatible porous supports by sol-gel synthesis for catalyst coatings, Appl. Catal. A 220 (2001) 79-92. 

Microstructure (see also Stereochemistry and Tacticity) 114,115.128.138,139 Miscibility (see also Compatibility) 12, 53, 68 Model networks 163 Modification of a polymer, chemical 154 Mold release 71, 74 Molecular weight, control 147. 154... 

The modern discipline of Materials Science and Engineering can be described as a search for experimental and theoretical relations between a material s processing, its resulting microstructure, and the properties arising from that microstructure. These relations are often complicated, and it is usually difficult to obtain closed-form solutions for them. For that reason, it is often attractive to supplement experimental work in this area with numerical simulations. During the past several years, we have developed a general finite element computer model which is able to capture the essential aspects of a variety of nonisothermal and reactive polymer processing operations. This "flow code" has been Implemented on a number of computer systems of various sizes, and a PC-compatible version is available on request. This paper is intended to outline the fundamentals which underlie this code, and to present some simple but illustrative examples of its use. 

The physical properties (7-10) of our E-V copolymers are sensitive to their microstructures. Both solution (Kerr effect or electrical birefringence) and solid-state (crystallinity, glass-transitions, blend compatibility, etc.) properties depend on the detailed microstructures of E-V copolymers, such as comonomer and stereosequence distribution. I3C NMR analysis (2) of E-V copolymers yields microstructural information up to and including the comonomer triad level. However, properties such as crystallinity depend on E-V microstructure on a scale larger than comonomer triads. 

In this chapter the technological development in cathode materials, particularly the advances being made in the material s composition, fabrication, microstructure optimization, electrocatalytic activity, and stability of perovskite-based cathodes will be reviewed. The emphasis will be on the defect structure, conductivity, thermal expansion coefficient, and electrocatalytic activity of the extensively studied man-ganite-, cobaltite-, and ferrite-based perovskites. Alterative mixed ionic and electronic conducting perovskite-related oxides are discussed in relation to their potential application as cathodes for ITSOFCs. The interfacial reaction and compatibility of the perovskite-based cathode materials with electrolyte and metallic interconnect is also examined. Finally the degradation and performance stability of cathodes under SOFC operating conditions are described. 

Each of the components of an SOFC stack anodes, cathodes, electrolytes, and interconnects must be thermally, chemically, mechanically, and dimensionally stable at the operating conditions and compatible with the other layers with which they come into contact in terms of thermal expansion and chemical inter-reaction. They must also have compatible processing characteristics. In addition to those requirements, the individual layers have additional microstructural, property, and processing target requirements, as summarized in Table 6.1. 

Once the structural support layers have been fabricated by extrusion or EPD for tubular cells or by tape casting or powder pressing for planar cells, the subsequent cell layers must be deposited to complete the cell. A wide variety of fabrication methods have been utilized for this purpose, with the choice of method or methods depending on the cell geometry (tubular or planar, and overall size) materials to be deposited and support layer material, both in terms of compatibility of the process with the layer to be deposited and with the previously deposited layers, and desired microstructure of the layer being deposited. In general, the methods can be classified into two very broad categories wet-ceramic techniques and direct-deposition techniques. 

Hence, catalysis related challenges for SOFC cathode are the development of cathode specifications, i.e., material and microstructure, having high catalytic activity for oxygen reduction at 600 °C, high electron and ion conductivity, and a low sensitivity for poisoning by volatile Cr species. Again, as for the anode, cost and compatibility related requirements have to be considered. 

This indicates that the PTFE particles are being pulled out of the matrix on application of stress. The microstructures of the corresponding CR composites measured by are shown in Fig. 45. The enhanced interfacial compatibility of modified PTFE particles in PTFE500kGy-CR is clearly visible in the corresponding micrographs. The modified agglomerate particles are embedded and partially enwrapped by the CR matrix. No clear and sharp interphase is... 

Unlike fibre- or whisker-reinforced composites, particulate composites have the advantage of being compatible with conventional powder processing, and in many cases can be pressurelessly sintered. As with other ceramic microstructures, a myriad of other ingenious fabrication routes have also been reported, but these are too numerous and system-specific to describe here. This section merely outlines the main points of powder processing where the production of composites in chemically compatible systems (i.e. those in which the components do not react chemically with one another) differs from that of monolithic ceramics. 

As with other ceramic composites, the combination of a- and/or P-sialon with reinforcement agents results in sialon composites. This simple and obvious statement encompasses many factors which must be taken into account for successfully fabricating composites with a designed microstructure and improved properties (Prewo, 1989). For sialon matrix composites, the most important factors are physical compatibility including Young s modulus, elastic strain (Kerans and Parthasarathy, 1991) and thermal expansion coefficient (Sambell etal., 1972a, b), and chemical compatibility between sialon matrix... 

The isolation of polynucleotides in microstructured devices provides a promising new approach that may be compatible with total integration of subsequent analytical steps and its current status is examined in the following sections. 

The system with which we have begun our investigations is the styrene-dimethylsiloxane system. The dimethylsiloxane blocks should be considerably less compatible with polystyrene blocks than either polybutadiene or polyisoprene since the solubility parameter of dimethylsiloxane is much farther from that of polystyrene than are the solubility parameters of polybutadienes or of polyisoprenes (17), no matter what their microstructure. Furthermore, even hexamers of polystyrene and of polydimethylsiloxane are immiscible at room temperature and have an upper critical-solution temperature above 35°C (18). In addition, the microphases in this system can be observed without staining and with no ambiguity about the identity of the phases in the transmission electron microscope (TEM) silicon has a much higher atomic number than carbon or oxygen, making the polydimethylsiloxane microphases the dark phases in TEM (19,20). 

Three diblock copolymers of cis-1,4 polyisoprene (IR) and 1,4-polybutadiene (BR) have been studied in dynamic mechanical experiments, transmission electron microscopy, and thermomechanical analysis. The block copolymers had molar ratios of 1/2, 1/1, and 2/1 for the isoprene and butadiene blocks. Homopolymers of polybutadiene and polyisoprene with various diene microstructures also were examined using similar experimental methods. Results indicate that in all three copolymers, the polybutadiene and polyisoprene blocks are essentially compatible whereas blends of homopolymers of similar molecular weights and microstructures were incompatible. 

As a final point regarding compatibility in BR/IR systems, we consider the effect of diene microstructure. In all of the experiments described above, microstructure was not a variable (Table I), with predominantly 1,4-addition appearing in both polymers. In this case it is possible that the incompatibility of the homopolymers might arise from the presence of the methyl group in the isoprene repeat unit and/or... 

The Feldman-Sereda model was based on the studies of sorption properties, porosities and relations between water content and physical properties. Alone among the proposed models, it is clearly compatible with the microstructural evidence and with the probable relationships between C-S-H gel and crystalline compounds. It is incompatible with that of Brunauer, but not with the essential features of that of Powers and Brownyard in its original form if the nature of the gel porosity is reinterpreted. Calculations of bound water (Section 7.3.3) indicate that about a third of the gel porosity of the Powers-Brownyard model is interlayer space, the remainder being micro or fine meso porosity of the kind shown in Fig. 8.4. However, as that figure illustrates, the boundary between interlayer space and micropores is ill defined. 

Lithium-Structure Compatibility. One of the critical chemistry problems of HYLIFE is the compatibility of structural alloys with the molten liquid of the jet array. Two candidate liquid metals are lithium and Pbg3Lij 7. High-Z metal (such as lead from target debris) will enter the liquid metal and may affect the compatibility. The structural alloy selected in the HYLIFE study is Cr-1 Mo, a ferritic steel. The carbides usually present in this steel are M3C (cementite) and M2C, where M is primarily Fe. Both of these carbides are unstable in lithium. M3C is usually present as platelets within pearlite, the eutectoid structure in pearlitic steel. The most common microstructure for the 2 4 Cr-1 Mo steel is large grains of ferrite with small islands of pearlite. M2C is present as a fine spray of precipitate within large ferrite grains. Lithium... 

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