Mass spectrometry of impact fragmented polymers: The role of target properties |
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Authors: | E.M. Mellado K. HornungR. Srama J. KisselS.P. Armes S. Fujii |
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Affiliation: | a Universität der Bundeswehr München LRT-7, D-85577 Neubiberg, Germanyb Max-Planck-Institut für Kernphysik, D-69117 Heidelberg, Germanyc Max-Planck-Institut für Sonnensystemforschung, D-37191 Katlenburg/Lindau, Germanyd Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, Yorkshire, S3 7HF, UKe Department of Applied Chemistry, Osaka Institute of Technology, Osaka 535-8585, Japan |
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Abstract: | Sulphur-containing latex micro-particles coated with an ultrathin conductive layer of polypyrrole have been accelerated in a van de Graff accelerator (up to 30 km/s) and impacted onto various target surfaces. These surfaces vary in their density (Ag and Au) as well as in their morphology by including highly porous nanostructured surfaces (“metal blacks”) in the study. After impact, the polymer chains of the latex particles are chemically degraded to much smaller molecular fragments. These fragments include both carbon- and sulphur-based species, which are detected as positive and negative ions by time-of-flight mass spectrometry. The mass spectra show that greater degradation occurs at higher velocities until finally only very simple molecular or atomic ions are formed. An effort is made to rationalise this strong velocity dependence based on energetic arguments. Furthermore, black surfaces lead to higher fragmentation than compact surfaces, which could be a consequence of much smaller impact spots. These results suggest organic molecule formation during expansion from the high pressure shock state. |
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Keywords: | Impact ionization Mass spectrometry Organics Nanostructures Cosmic dust |
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