1,451 research outputs found
REPORT drawn up on behalf of the Political Affairs Committee on the enlargement of the Community to include Spain and Portugal Section I: Report on the conclusion of the negotiations with Spain and Portugal. EP Working Documents 1985-86, document 2-20/85, 24 April 1985
Report drawn up on behalf of the Political Affairs Committee on political relations between the European Community and the United States of America. EP Working Documents 1983-1984, Document 1-1540/83/A, 19 March 1984
Report drawn up on behalf of the Political Affairs Committee on relations between the European Parliament and the Council of the Community. EP Working Documents 1981-82, Document 1-216/81, 27 May 1981
Tunneling Ionization Rates from Arbitrary Potential Wells
We present a practical numerical technique for calculating tunneling
ionization rates from arbitrary 1-D potential wells in the presence of a linear
external potential by determining the widths of the resonances in the spectral
density, rho(E), adiabatically connected to the field-free bound states. While
this technique applies to more general external potentials, we focus on the
ionization of electrons from atoms and molecules by DC electric fields, as this
has an important and immediate impact on the understanding of the multiphoton
ionization of molecules in strong laser fields.Comment: 13 pages, 7 figures, LaTe
Time-dependent calculation of ionization in Potassium at mid-infrared wavelengths
We study the dynamics of the Potassium atom in the mid-infrared, high
intensity, short laser pulse regime. We ascertain numerical convergence by
comparing the results obtained by the direct expansion of the time-dependent
Schroedinger equation onto B-Splines, to those obtained by the eigenbasis
expansion method. We present ionization curves in the 12-, 13-, and 14-photon
ionization range for Potassium. The ionization curve of a scaled system, namely
Hydrogen starting from the 2s, is compared to the 12-photon results. In the
13-photon regime, a dynamic resonance is found and analyzed in some detail. The
results for all wavelengths and intensities, including Hydrogen, display a
clear plateau in the peak-heights of the low energy part of the Above Threshold
Ionization (ATI) spectrum, which scales with the ponderomotive energy Up, and
extends to 2.8 +- 0.5 Up.Comment: 15 two-column pages with 15 figures, 3 tables. Accepted for
publication in Phys. Rev A. Improved figures, language and punctuation, and
made minor corrections. We also added a comparison to the ADK theor
Dual Action Additives for Jet A-1: Fuel Dehydrating Icing Inhibitors
© 2016 American Chemical Society. A novel approach for protecting jet fuel against the effects of water contamination based upon Fuel Dehydrating Icing Inhibitors (FDII) is presented. This dual-action strategy is predicated on the addition of a fuel-soluble water scavenger that undergoes a kinetically fast hydrolysis reaction with free water to produce a hydrophilic ice inhibitor, thereby further militating against the effects of water crystallization. Criteria for an optimum FDII were identified and then used to screen a range of potential water-scavenging agents, which led to a closer examination of systems based upon exo/endo-cyclic ketals and both endo- and exo-cyclic ortho esters. The ice inhibition properties of the subsequent products of the hydrolysis reaction in Jet A-1 were screened by differential scanning calorimetry. The hydrolysis products of 2-methoxy-2-methyl-1,3-dioxolane demonstrate similar ice inhibition performance to DiEGME over a range of blend levels. The calorific values for the products of hydrolysis were also investigated, and it is clear that there would be a significant fuel saving on use of the additive over current fuel system icing inhibitors. Finally, three promising candidates, 2-methoxy-2-methyl-1,3-dioxolane, 2-methoxy-2-methyl-1,3-dioxane, and 2-methoxy-2,4,5-trimethyl-1,3-dioxolane, were shown to effectively dehydrate Jet A-1 at room temperature over a 2 h period
Mechanisms of base selection by human single-stranded selective monofunctional uracil-DNA glycosylase
hSMUG1 (human single-stranded selective monofunctional uracil-DNA glyscosylase) is one of three glycosylases encoded within a small region of human chromosome 12. Those three glycosylases, UNG (uracil-DNA glycosylase), TDG (thymine-DNA glyscosylase), and hSMUG1, have in common the capacity to remove uracil from DNA. However, these glycosylases also repair other lesions and have distinct substrate preferences, indicating that they have potentially redundant but not overlapping physiological roles. The mechanisms by which these glycosylases locate and selectively remove target lesions are not well understood. In addition to uracil, hSMUG1 has been shown to remove some oxidized pyrimidines, suggesting a role in the repair of DNA oxidation damage. In this paper, we describe experiments in which a series of oligonucleotides containing purine and pyrimidine analogs have been used to probe mechanisms by which hSMUG1 distinguishes potential substrates. Our results indicate that the preference of hSMUG1 for mispaired uracil over uracil paired with adenine is best explained by the reduced stability of a duplex containing a mispair, consistent with previous reports with Escherichia coli mispaired uracil-DNA glycosylase. We have also extended the substrate range of hSMUG1 to include 5-carboxyuracil, the last in the series of damage products from thymine methyl group oxidation. The properties used by hSMUG1 to select damaged pyrimidines include the size and free energy of solvation of the 5-substituent but not electronic inductive properties. The observed distinct mechanisms of base selection demonstrated for members of the uracil glycosylase family help explain how considerable diversity in chemical lesion repair can be achieved
Beyond Implications and Applications: the Story of ‘Safety by Design’
Using long-term anthropological observations at the Center for Biological and Environmental Nanotechnology in Houston, Texas, the article demonstrates in detail the creation of new objects, new venues and new modes of veridiction which have reoriented the disciplines of materials chemistry and nanotoxicology. Beginning with the confusion surrounding the meaning of ‘implications’ and ‘applications’ the article explores the creation of new venues (CBEN and its offshoot the International Council on Nanotechnology); it then demonstrates how the demands for a responsible, safe or ethical science were translated into new research and experiment in and through these venues. Finally it shows how ‘safety by design’ emerged as a way to go beyond implications and applications, even as it introduced a whole new array of controversies concerning its viability, validity and legitimacy
Resonant enhancements of high-order harmonic generation
Solving the one-dimensional time-dependent Schr\"odinger equation for simple
model potentials, we investigate resonance-enhanced high-order harmonic
generation, with emphasis on the physical mechanism of the enhancement. By
truncating a long-range potential, we investigate the significance of the
long-range tail, the Rydberg series, and the existence of highly excited states
for the enhancements in question. We conclude that the channel closings typical
of a short-range or zero-range potential are capable of generating essentially
the same effects.Comment: 7 pages revtex, 4 figures (ps files
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