The paper describes a theory of particle deposition based formally on
the conservation
equations of particle mass and momentum. These equations are formulated in an
Eulerian coordinate system and are then Reynolds averaged, a procedure which
generates a number of turbulence correlations, two of which are of prime importance.
One represents ‘turbulent diffusion’ and the other
‘turbophoresis’, a convective drift
of particles down gradients of mean-square fluctuating velocity. Turbophoresis is
not a small correction; it dominates the particle dynamic behaviour in the
diffusion-impaction and inertia-moderated regimes.Adopting a simple model for the turbophoretic force, the theory is used to
calculate
deposition from fully developed turbulent pipe flow. Agreement with experimental
measurements is good. It is found that the Saffman lift force plays an important role
in the inertia-moderated regime but that the effect of gravity on deposition from
vertical flows is negligible. The model also predicts an increase in particle
concentration
close to the wall in the diffusion-impaction regime, a result which is partially
corroborated by an independent ‘direct numerical simulation’ study.The new deposition theory represents a considerable advance in physical
understanding over previous free-flight theories. It also offers many avenues
for future
development, particularly in the simultaneous calculation of laminar (pure inertial)
and turbulent particle transport in more complex two- and three-dimensional
geometries.
The paper discusses the classical theory of the homogeneous nucleation of water droplets from supersaturated vapour and its application in predicting condensation in steam nozzles. The first part consists of a review of classical nucleation theory, focusing on the many modifications made to the original Becker-Döring theory and providing some new insights into recent developments. It is concluded that the predictive accuracy required for engineering calculations is not yet attainable with a theory derived from first principles. The areas that require most attention relate to the properties of small molecular clusters and the energy transfer processes in the non-isothermal theory. Experiments in converging-diverging nozzles provide the best means for validation at the very high nucleation rates of interest, but measurements of pressure distribution and the Sauter mean droplet radius are insufficient to provide independent checks on the separate theories of nucleation and droplet growth. Nevertheless, a judicious choice for the nucleation rate equation, in combination with a standard droplet growth model and a suitable equation of state for steam, can provide accurate predictions over a wide range of conditions. The exception is at very low pressures where there is evidence that the droplet growth rate in the nucleation zone is underestimated.
The paper describes a method of computing nonequilibrium, steady flows of wet steam in two- and quasi-three-dimensional turbine cascades. The mixture conservation equations are solved in an Eulerian reference frame using an inviscid time-marching method that includes the effects of the centrifugal and Coriolis acceleration terms in rotating blade rows. Nucleation and growth of water droplets are computed by integrating the relevant equations along true streamlines in a Lagrangian reference frame. Steam properties are computed using equations that display commercial steam table accuracy for pressures below 10 bar. Special procedures for grouping the range of droplet sizes present are described that allow an accurate representation of the droplet size distribution to be retained without requiring a large increase in CPU time. All types of wet-steam flow, including those involving secondary nucleation, can be computed. Examples are presented that display the sensitivity of the calculation procedure in computing nucleation affected by the shock- and expansion-wave structure in the region of a turbine blade trailing edge. Typical CPU time requirements for nonequilibrium solutions involving primary or secondary nucleations are about three times those for perfect gas calculations.
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