Measurements reveal electron drift velocities and ionization coefficients in THF, indicating clustering effects in mixtures with H2O.
The flux electron drift velocity and longitudinal diffusion coefficients, the effective ionisation coefficients and the reaction rates have been measured for Tetrahydrofuran (THF, C 4 H 8 O) and its mixtures with H 2 O in the gaseous phase, using a Pulsed Townsend Apparatus. A wide range of gas pressures up to 90 Torr, and of the density-normalized electric field intensity, E/N, from 1 to 260 Td (1 Townsend=10 -17 V cm 2 ) were covered. The electron drift velocities and effective ionisation coefficients for pure THF have been fully re-measured, particularly those belonging to the electron attachment region. The measured electron drift velocity curves of the THF-H 2 O mixtures show a peculiar crossover at around E/N=65 Td, for which a thorough explanation is offered, using the two-term simulation code Bolsig+, and a selected group of electron-THF and electron-H 2 O cross sections. The electron drift velocities for THF, H 2 O and their mixtures were calculated successfully with mean deviations from the measured values with a correlation coefficient above 0.99. The electron attachment coefficient in THF was measured from 1 to 70 Td. We found no clear indication of a negative-ion dissociation region and provide an explanation to this finding. The longitudinal diffusion coefficient and the effective ionisation rates for the THF-H 2 O mixtures containing 10% to 90% H 2 O were also measured. The drift and reactions of negative ions in pure THF were measured over the low E/N range 8-14 Td. The clear pressure dependence of the measured negative-ion drift velocities and reduced mobilities, led us to formulate a simple theoretical model to calculate the measurable current, thereby rendering an apparent clustering coefficient. No mass identification was possible.
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ROMERO et al. (2025) studied this question.
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