ABSTRACT
The application of finely divided (black) Pd and Pd-Fe powder in the sono-electro-catalytic reduction of chlorophenoxy herbicides (2,4-D) and chlorophenols (2,4-DCP) in aqueous solutions allows for effective destruction of toxic chlorinated aromatic compounds. At 20 degrees C complete conversion of these compounds is observed within 10 min. On bimetallic Pd/Fe catalyst, intermediates due to the oxidation reaction are detected in addition to the products of dechlorination. The bimetallic catalyst appears to be energetically and economically superior to the Pd. In both cases, the reaction times were considerably shortened in comparison with traditional electro-catalytic processes.
Subject(s)
Hydrocarbons, Chlorinated/analysis , Ultrasonics , Water Pollutants, Chemical/analysis , Water Purification/methods , Catalysis , Electrochemistry , Iron/chemistry , Palladium/chemistry , PowdersABSTRACT
Experimental results are presented for the scattering of well-defined beams of molecular oxygen incident on clean Al(111). The data consist of scattered angular distributions measured as a function of incident angle, and for fixed incident angle, the dependence on surface temperature of the angular distributions. The measurements are interpreted in terms of a scattering theory that treats the exchange of energy between the translational and rotational motions of the molecule and the phonons of the surface using classical dynamics. The dependence of the measured angular distributions on incident beam angle and temperature is well explained by the theory. Rotational excitation and quantum excitation of the O(2) internal stretching mode are briefly discussed.
ABSTRACT
The structure formation upon spinodal decomposition of a two-dimensional model system, a Au adatom gas on a Au(111) surface, was observed in situ by scanning tunneling microscopy (STM). A thermodynamically unstable state was prepared by applying microsecond voltage pulses to the STM tip in an electrochemical system, causing the random dissolution of Au atoms from the uppermost monolayer. Interconnected, labyrinthine island patterns were formed at Au coverages between 0.4 and 0.9 monolayer with dominating length scales lambda(m) of the order of a few nanometers.