Scalar dissipation rates in non-conservative transport systems.
Scalar dissipation rates in non-conservative transport systems.
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DOI:
10.1016/j.jconhyd.2013.03.003
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发表时间:
2013-06
影响因子:
3.6
通讯作者:
Fogg, Graham E.
中科院分区:
文献类型:
--
作者:
Engdahl, Nicholas B.;Ginn, Timothy R.;Fogg, Graham E.
This work considers how the inferred mixing state of diffusive and advective-diffusive systems will vary over time when the solute masses are not constant over time. We develop a number of tools that allow the scalar dissipation rate to be used as a mixing measure in these systems without calculating local concentration gradients. The behavior of dissipation rates are investigated for single and multi-component kinetic reactions and a commonly studied equilibrium reaction. The scalar dissipation rate of a tracer experiencing first order decay can be determined exactly from the decay constant and the dissipation rate of a passive tracer, and the mixing rate of a conservative component is not the superposition of the solute specific mixing rates. We then show how the behavior of the scalar dissipation rate can be determined from a limited subset of an infinite domain. Corrections are derived for constant and time dependent limits of integration the latter is used to approximate dissipation rates in advective-diffusive systems. Several of the corrections exhibit similarities to the previous work on mixing, including non-Fickian mixing. This illustrates the importance of accounting for the effects that reaction systems or limited monitoring areas may have on the inferred mixing state.
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