The structure of the zone of diffusion controlled reaction
โ Scribed by S.K. Friedlander; K.H. Keller
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- English
- Weight
- 696 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0009-2509
No coin nor oath required. For personal study only.
โฆ Synopsis
In the theory of the chemical reaction controlled (macroscopically) by diffusion it is assumed that the concentration gradient is discontinuous at the reaction zone. The theory works best for fast reactions for which the zone of reaction is extremely thin. Since reaction rates are finite, the zone of reaction must in reality have finite thickness and possess a structure with respect to the concentration and its gradient.
In this paper, the differential equation describing the concentration distribution in the reaction zone for very fast, but not infinitely fast, reactions is set up for second-and third-order kinetics. Similarity transformations which eliminate all dimensional constants are given for both sets of equations and boundary conditions. A solution obtained for the isothermal second order case using an analog computer is given. A reaction zone thickness is defined and used to establish the conditions under which transport from a dissolving, reacting sphere is diffusion controlled. A numerical calculation is given for the case of a CO2 bubble dissolving in an hydroxide solution.
By measuring the thickness of the reaction zone it should be possible to estimate the rates of reactions in solution. An example is given for the reaction occurring in a capillary connecting reservoirs containing solutions of the two reactants.
๐ SIMILAR VOLUMES
Analysis of the temperature and composition profiles obtained by probing a confined, axisymmetric-laminar methaneair diffusion flame suggests that a state of partial equilibrium exists in the high-temperature primary reaction zone. Free-radical concentrations were estimated to be several orders of m
We consider the initial-value problem for the nonlinear parabolic equation with u, -a(u")\\_ + bd = 0, -coo u(x,O) = t&(x). -w < x < m ) and a > 0, b E R', m 2 1, ,B > 0 The inital function has finite support and is supposed to be nonnegative, and continuous. Locating the right-hand edge of the supp
The competitive, consecutive reations A + B = J?, R + B = S are considered to occur within spherical or planar zones, initially containing only the reagent B and into which the reagent A diffuses. Depending upon whether B is immobile or can diffuse within the reaction zone, so will different distrib