@article {4442,
	title = {An investigation of dynamical density functional theory for solvation in simple mixtures},
	journal = {Journal of Chemical Physics},
	volume = {108},
	number = {15},
	year = {1998},
	note = {ISI Document Delivery No.: ZH114Times Cited: 27Cited Reference Count: 48},
	month = {Apr},
	pages = {6378-6386},
	type = {Article},
	abstract = {Linear and nonlinear versions of time dependent density functional theory are solved for a single solute particle in a simple binary solvent. All particles interact with Lennard-Jones potentials. The theoretical results are compared with molecular dynamics calculations. It is shown that the nonlinear theory is necessary in order to obtain a good quantitative description of selective solvation dynamics. The linear theory is only of qualitative value. Also, attention is drawn to a previously little appreciated problem which arises when one attempts to compare time dependent density functional theory with computer simulation or experimental results. The difficulty involves matching the theoretical and absolute time scales and is discussed in detail in this paper. (C) 1998 American Institute of Physics. [S0021-9606(98)50615-0].},
	keywords = {BINARY DIPOLAR LIQUIDS, COLLECTIVE ORIENTATIONAL RELAXATION, density, DIELECTRIC-RELAXATION, ELECTROLYTE-SOLUTIONS, ION SOLVATION, MOLECULAR THEORY, NONPOLAR SOLVATION, NUMBER, POLAR, SURROGATE HAMILTONIAN DESCRIPTION},
	isbn = {0021-9606},
	url = {<Go to ISI>://000073073700034},
	author = {Yoshimori, A. and Day, T. J. F. and Patey, G. N.}
}
@article {3198,
	title = {THE RESPONSE OF THE INDUCTIVELY-COUPLED ARGON PLASMA TO SOLVENT PLASMA LOAD - SPATIALLY-RESOLVED MAPS OF ELECTRON-DENSITY OBTAINED FROM THE INTENSITY OF ONE ARGON LINE},
	journal = {Spectrochimica Acta Part B-Atomic Spectroscopy},
	volume = {49},
	number = {12-14},
	year = {1994},
	note = {ISI Document Delivery No.: QD364Times Cited: 13Cited Reference Count: 40},
	month = {Oct-Dec},
	pages = {1231-1250},
	type = {Article},
	abstract = {A survey of spatially resolved electron number density (n(e)) in the tail cone of the inductively coupled argon plasma (ICAP) is presented: all of the results of the survey have been radially inverted by numerical, asymmetric Abel inversion. The survey extends over the entire volume of the plasma beyond the exit of the ICAP torch; It extends over distances of z = 5-25 mm downstream from the induction coil, and over radial distances of +/- 8 mm from the discharge axis. The survey also explores a range of inner argon flow rates (Q(IN)), solvent plasma load (Q(SPL)) and r.f. power: moreover, it explores loading by water, methanol and chloroform. Throughout the survey, n(e) was determined from the intensity of one, optically thin argon line, by a method which assumes that the atomic state distribution function (ASDF) for argon lies close to local thermal equilibrium (LTE). The validity of this assumption is reviewed. Also examined are the discrepancies between n(e) from this method and n(e) from Stark broadening measurements. With the error taken into account, the results of the survey reveal how time averaged values of n(e) in the ICAP respond over an extensive, previously unexplored range of experimental parameters. Moreover, the spatial information lends insight into how the thermal conditions and the transport of energy respond. Overall, the response may be described in terms of energy consumption along the axial channel and thermal pinch within the induction region. The predominating effect depends on the solvent plasma load, the solvent composition, the robustness of the discharge, and the distribution of solvent material over the argon stream.},
	keywords = {ATOMIC EMISSION-SPECTROMETRY, DESOLVATION, EQUILIBRIUM, EXCITATION, GAS-FLOW, INTRODUCTION, NUMBER, SAMPLE, STATE DISTRIBUTION FUNCTION, TEMPERATURE DETERMINATION, WATER},
	isbn = {0584-8547},
	url = {<Go to ISI>://A1994QD36400009},
	author = {Weir, D. G. J. and Blades, M. W.}
}
