Metal oxides, thermal expansion

Aluminum-containing propellants deflver less than the calculated impulse because of two-phase flow losses in the nozzle caused by aluminum oxide particles. Combustion of the aluminum must occur in the residence time in the chamber to meet impulse expectations. As the residence time increases, the unbumed metal decreases, and the specific impulse increases. The soHd reaction products also show a velocity lag during nozzle expansion, and may fail to attain thermal equiUbrium with the gas exhaust. An overall efficiency loss of 5 to 8% from theoretical may result from these phenomena. However, these losses are more than offset by the increase in energy produced by metal oxidation (85—87). 

Fretting corrosion (36,37) can lead to high contact resistance of base metal contacts, such as tin plate in electronic connectors. Small cycHcal displacements of the connector halves occur because of external vibration or differential thermal expansion and contraction of the mating contacts. The wear debris that is formed remains in the contact zone. The accumulation of oxide debris in the contact region leads to increased contact resistance. Solutions to this problem are stmctures that do not permit movement of contact surfaces with respect to one another, the use of gold as a contact finish, and the appHcation of thick coatings of contact lubricants and greases, which reduce the rate of wear and restrict access of air to the contact surfaces. 

The ceramic oxide carrier is bonded to the monolith by both chemical and physical means. The bonding differs for a ceramic monolith and a metallic monolith. Attrition is a physical loss of the carrier from the monolith from the surface shear effects caused by the exhaust gas, a sudden start-up or shutdown causing a thermal shock as a result of different coefficients of thermal expansion at the boundary between the carrier and the monolith, physical vibration of the cataly2ed honeycomb, or abrasion from particulates in the exhaust air (21) (see Fig. 6d). 

The viscosity of liquid silicates such as drose containing barium oxide and silica show a rapid fall between pure silica and 20 mole per cent of metal oxide of nearly an order of magnitude at 2000 K, followed by a slower decrease as more metal oxide is added. The viscosity then decreases by a factor of two between 20 and 40 mole per cent. The activation energy for viscous flow decreases from 560 kJ in pure silica to 160-180kJmol as the network is broken up by metal oxide addition. The introduction of CaFa into a silicate melt reduces the viscosity markedly, typically by about a factor of drree. There is a rapid increase in the thermal expansivity coefficient as the network is dispersed, from practically zero in solid silica to around 40 cm moP in a typical soda-lime glass. 

Fillers are used in tooling and casting application. Not only do they reduce cost but in diluting the resin content they also reduce curing shrinkage, lower the coefficient of expansion, reduce exotherms and may increase thermal conductivity. Sand is frequently used in inner cores whereas metal powders and metal oxide fillers are used in surface layers. Wire wool and asbestos are sometimes used to improve impact strength. 

Under thermal cycling conditions, the principal source of stress within the oxide scale is the temperature change . Christl et have noted that, when cooling 2.25%Cr-l%Mo steel from 600°C in air, compressive stresses build up in the haematite, whilst tensile stresses build up in the magnetite and spinel layers. This arises because the thermal expansion coefficients of the individual oxide layers increase in the order a metal < a spinel < a magnetite < a haematite . ... 

The major use of boric acid is as the starting material for its anhydride, boron oxide, B203. Because it melts (at 450°C) to a liquid that dissolves many metal oxides, boron oxide (often as the add) is used as a flux, a substance that cleans metals as they are soldered or welded. Boron oxide is also used to make fiberglass and borosilicate glass, a glass with a very low thermal expansion, such as Pyrex (see Section 14.21). 

Where a chrect fusion of glass-to-metal or metal oxide is obtained (sometimes termed the wetting of metal by glass) two types of seal can result—one matched, the other mismatched, depending on how the relative coefficients of thermal expansion of the glass and the metal compare. 

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. 

It has been observed that solid oxide fuel cell voltage losses are dominated by ohmic polarization and that the most significant contribution to the ohmic polarization is the interfacial resistance between the anode and the electrolyte (23). This interfacial resistance is dependent on nickel distribution in the anode. A process has been developed, PMSS (pyrolysis of metallic soap slurry), where NiO particles are surrounded by thin films or fine precipitates of yttria stabilized zirconia (YSZ) to improve nickel dispersion to strengthen adhesion of the anode to the YSZ electrolyte. This may help relieve the mismatch in thermal expansion between the anode and the electrolyte. 

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