Portfolio optimization problem under concave transaction costs and minimal transaction unit constraints

We will propose a branch and bound algorithm for calculating a globally optimal solution of a portfolio construction/rebalancing problem under concave transaction costs and minimal transaction unit constraints. We will employ the absolute deviation of the rate of return of the portfolio as the measure of risk and solve linear programming subproblems by introducing (piecewise) linear underestimating function for concave transaction cost functions. It will be shown by a series of numerical experiments that the algorithm can solve the problem of practical size in an efficient manner. Received: July 15, 1999 / Accepted: October 1, 2000?Published online December 15, 2000     

Portfolio optimization under D.C. transaction costs and minimal transaction unit constraints

This paper addresses itself to a portfolio optimization problem under nonconvex transaction costs and minimal transaction unit constraints. Associated with portfolio construction is a fee for purchasing assets. Unit transaction fee is larger when the amount of transaction is smaller. Hence the transaction cost is usually a concave function up to certain point. When the amount of transaction increases, the unit price of assets increases due to illiquidity/market impact effects. Hence the transaction cost becomes convex beyond certain bound. Therefore, the net expected return becomes a general d.c. function (difference of two convex functions). We will propose a branch-and-bound algorithm for the resulting d.c. maximization problem subject to a constraint on the level of risk measured in terms of the absolute deviation of the rate of return of a portfolio. Also, we will show that the minimal transaction unit constraints can be incorporated without excessively increasing the amount of computation.     

A direct correspondence between charge transfer to solvent spectra and electrochemical data and theories: a linear relationship up to 10 mol dm−3 and precise madelung constants from spectral shift data

The shift in E_max for the CTTS spectrum of iodide on addition of alkali chlorides is definitively related to their mean activity coefficients. The relative contributions to the coulombic interaction of the Debye—Hückel and expanded-lattice models are determined by a new precise procedure, yielding accurate Madelung constants.