Solidification can occur under many different conditions. The experimental situation being considered here is an undercooled two component liquid with a simple binary eutectic phase diagram where the system can be held at constant temperature $T_o$ as solidification proceeds. To simplify the notation, $NH_4Cl$ will be referred to as A, and $H_2O$ will be referred to as B in the remainder of this chapter (Fig. \ref{fig:gen_ph_diag}). \begin{figure}[thp] \includegraphics[angle=0,scale=.90]{mickey.eps} \caption{The generalized phase diagram, to which will be referred in this chapter. A can be thought of as representing $NH_4Cl$ and B can be thought of as representing $H_2O$.} \label{fig:gen_ph_diag} \end{figure} The system's initial concentration of B (impurity) is $C_o$. When solid forms, it consists entirely of A, requiring that all of the B is rejected into the liquid. This raises the concentration of B in the liquid above $C_o$. Additionally, although it is initially thermodynamically favorable throughout the entire system for solid A to precipitate from the liquid (rejecting B into solution as it grows), the initial solid must be nucleated. Further growth then takes place off the prexistent solid. These conditions were all very nearly satisfied in the experimental system studied in chapter X, and were strictly enforced in the cellular automata model of chapter Y resulting in extremely good qualitative agreement with the experiments. The experiment was constructed to be as two-dimensional as possible to facilitate the rapid extraction of any generated heat. Insights from these 2D systems have led to the PDE's described here, and the following derivation will thus also be in 2D, although it can easily be treated in 1D or in 3D. In the latter case, one needs to consider the temperature field and potentially any gravity-driven convection in the melt \cite{Poirier:94, Chiareli:94}. Before beginning the PDE derivation, it is a good idea to have a picture of the dynamics. When the solid is growing, there appears to be a moving envelope, behind which there is an array of dendrites, and ahead of which is liquid (Figures A and B). It is important to realize that the impurity B can diffuse through the liquid parts but not through the solid parts (or at best, only very slowly through the solid). The solid therefore acts as a diffusional barrier to the impurity. In fact, the structure/morphology of the growing array of dendrites, in the absence of significant fluid flow, is expected to dictate the speed and shape of this envelope. Within the dendritic array itself, there are two distinct states of matter: the actual dendrites made up of solid A; and the liquid portion in between these dendrites. Since the impurity B is rejected from the solid into the liquid portion, one expects this interdendritic liquid to be higher in concentration of the impurity B than the original liquid before any solidification began. In fact, the cellular automata model of chapter X shows that the higher the concentration of impurity B in this interdendritic liquid, the faster the structure propagates into the unsolidified liquid. This means that the more effectively the needle structure can entrain/contain the impurity B, the less this impurity is able to escape the solid network and get ahead of the interface. With a lower concentration of B ahead of the front, the driving force for solidification is higher and solid will grow more quickly in the form of a denser dendritic network. With this in mind, the discussion of the PDE derivation can begin.