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Kowalski, Benjamin A.

Publications and source records attributed to Kowalski, Benjamin A..

Thermodynamic Measurements Using the Knudsen Cell Technique

The Knudsen cell technique has been used for over a century and is a valuable tool for measurement of vapor pressures and thermodynamic properties. It is based on a small enclosure (~1 cm long x 1 cm diameter) in which a condensed phase/vapor equilibria can be established. A small (<1 mm) orifice on the cell allows sampling of the vapor via a variety of techniques including weight loss, torsion effusion, target collection, and mass spectrometry. Many excellent measurements based on these methods have been reported. However in order to obtain reliable measurements, a variety of factors must be considered. They include proper cell material selection, accurate and uniform temperature control and measurement, and proper sampling of the vapor. Each of these factors are discussed in detail in this chapter. Typically these studies are conducted at high temperatures and it is a challenge to select an inert container material. Recommended materials are discussed and in some cases the container may be used as part of the system under study. Temperature control and measurement is perhaps the most important issue. In most systems, the furnace must be compact yet there can be no temperature gradient in the cell. Temperatures are measured with either a thermocouple or pyrometer and the relative advantages of each are discussed. Sampling method considerations depend on the particular technique. It is essential that all of the vapor or a representative portion of the vapor be sampled. The distribution of the effusate from a Knudsen cell is discussed and sampling positions discussed. Mass spectrometry is often used to study the effusing vapor and the relations between ion current and vapor pressure are discussed.

mass spectrometry

Calorimetric Measurements of the Thermodynamic Properties of RE-Silicate Coating Materials

Thermodynamic quantities of coatings materials and siliceous debris-induced corrosion products are crucial to understand in order to develop mitigation strategies necessary to improve the durability of gas-turbine engines. Siliceous induced corrosion can occur when debris consisting mainly of CaO-MgO-Al2O3-SiO2 (CMAS) is ingested by aircraft engines during and after take-off, which sticks to hot surfaces and forms calcium rare-earth silicate oxyapatites. In this work, high-temperature oxide melt drop solution calorimetry (HT drop solution calorimetry) was used to obtain the enthalpies of formation for RE silicate (RE2Si2O7, RE2SiO5 where RE = Yb, Er, Y, Dy, Nd, Lu and Gd) environmental barrier coatings (EBCs) and the calcium RE silicate oxyapatite Ca2RE8(SiO4)6O2 (RE = Yb, Er, Y, Dy, Nd, Gd and Sm) corrosion products. Trends in the enthalpy of formation as a function of the ionic potential of the rare-earth cations in their related crystallographic sites are discussed.

Costa, Gustavo

Novel Environmental Barrier Coatings for the Protection of SiC Components

Greater gas turbine engine efficiency is a major goal in aeronautics research often pursued through increased engine operating temperatures. However, it is necessary to replace the current hot-stage alloy components with more thermally robust parts, such as Silicon-based ceramics and composites. Unfortunately, these materials are still susceptible to the effects of oxidation, water vapor, and (Calcium-Magnesium-Alumino-Silicate) CMAS interaction, among other issues at high temperature. To mitigate these effects, environmental barrier coating (EBC) materials are employed to help control the rate of degradation to the underlying composite, but must also survive the corrosive environment. The current study explores new design space in Mg-based EBC materials with respect to microstructure, high temperature phase stability, volatilization in water vapor, as well as structure-property relationships at high temperature.

Kowalski, Benjamin A.

High Temperature Vaporization into Different Environments

Materials in extreme environments are often negatively affected by the process of vaporization. The maximum vaporization rate is determined by calculating a flux from the equilibrium vapor pressure(s) of each component. However, this maximum vaporization flux is decreased by the vaporization coefficient and the atmosphere above the material. This paper discusses each of these factors for common oxides, using SiO2 as an example. Vaporization into a vacuum is an ideal starting point, as the basic mechanisms for vaporization have been derived from these studies. Imposing an over-pressure of a static gas changes the vaporization rates from both a thermodynamic and kinetic aspect. Finally, a flowing gas is the most common situation encountered in many extreme environments. Laminar and turbulent flow effects are be treated with both analytical transport expressions and computational fluid dynamics (CFD). The example of a vaporizing SiO2 coupon in a laboratory furnace is examined with both the analytical expressions and with CFD.

Jacobson, Nathan