Intermediate LET-like effect in distal part of proton Bragg peak revealed by track-ends imaging during super-Fricke radiolysis.

Upstream of the efficiency of proton or carbon ion beams in cancer therapy, and to optimize hadrontherapy results, we analysed the chemistry of Fricke solutions in track-end of 64-MeV protons and 1.14-GeV carbon ions. An original optical setup is designed to determine the primary track-segment yields along the last millimetres of the ion track with a sub-millimetre resolution. The Fe3+-yield falls in the Bragg peak to (4.9 ± 0.4) × 10-7 mol/J and 1.9 × 10-7 mol/J, under protons and carbon ions respectively. Beyond the Bragg peak, a yield recovery is observed over 1 mm for proton beams. It is attributed to the intermediate-LET of protons in this region where their energy decreases and energy distribution becomes broader, in relation with the longitudinal straggling of the beam. Consequently to this LET decrease in the distal part of the Bragg peak, Fe3+-yield increases. For the first time, this signature is highlighted at the chemical level under proton irradiation. Nevertheless, this phenomenon is not identified for carbon ion beams since their straggling is lower. It would need a greater spatial resolution to be observed.

In situ and time-resolved infrared detection of the reactivity induced by electrons in polymer films.

The real time and in situ analysis of chemical reactions such as polymerization reactions, polymer degradation, and oxidation of polymers is of utmost importance. Surprisingly, only few experimental tools allowing this are available. To bridge this gap, we have developed a new experimental setup coupling a 60 keV electron gun with an infrared spectrometer operating in the mid-IR region (800-4000 cm-1) and associated with the rapid scan mode. The measurements are performed using the infrared reflection absorption spectroscopy approach. We worked here with 0.5-25 ms pulses for which the dose per pulse ranges from 4 to 200 kGy. Combining pulse electrons with rapid scan analysis enables performing experiments with a time resolution of 80 ms (and above). Therefore, this new platform can, for instance, give direct insights into reaction mechanisms at stake during the degradation of polymers. First results on a bisphenol A polycarbonate irradiated under vacuum enabling the validation of this new setup and also the recording of time-resolved spectra are presented. Reaction mechanisms are then proposed.

Hydrogen Emission and Macromolecular Radiation-Induced Defects in Polyethylene Irradiated under an Inert Atmosphere: The Role of Energy Transfers toward trans-Vinylene Unsaturations.

This article is aimed at studying the evolution of H2 release as well as radiation-induced defects in polyethylene (PE), as a function of the irradiation dose under anoxic conditions. We analyze the influence of the energy transfers and trapping toward radiation-induced defects on the evolution of the radiation chemical yields with dose. One key objective herein is to quantify the contribution of these transfers toward trans-vinylene (TV) on H2 emission. For this purpose, pure PE was irradiated in a large dose domain and H2 emission was compared to that in predoped PEs containing chemically inserted TV groups irradiated at low doses. In parallel, evolutions of the concentrations of the TV groups and minor defects (vinyl and trans-trans-diene) as a function of dose were considered. Moreover, measuring simultaneously H2 and unsaturated groups had allowed inferring the cross-linking evolution with dose. With this methodology, we have succeeded in quantifying the efficiency of TVs and cross-links as energy traps and, using simple models, in fully describing the evolution of all of the radiation chemical yields. Besides, irradiations were performed using either low linear energy transfer irradiations (electron beams, γ rays) or ion beams, with the objective to assess the influence of the high ionization and excitation densities induced by the latter on PE ageing and energy transfer processes.

Aliphatic/aromatic systems under irradiation: influence of the irradiation temperature and of the molecular organization.

With the aim of understanding the electronic excitation, charge or reactive species transfers occurring during irradiation, we studied the role of the aromatic content on ethylene/styrene random copolymers (PES) and on cyclohexane/benzene glasses (amorphous organic solids). Radiation-induced modifications were monitored in situ, at the molecular level, using Fourier transform infrared spectroscopy (FTIR). Irradiations were performed under a vacuum, and thanks to in situ measurements, oxidation was avoided. We followed both the C═C bond creation in the aliphatic moiety and the destruction of the aromatic moiety. The influence of the irradiation temperature was investigated by irradiating samples at room temperature and at 11 K. At such a low temperature, long-range migration hardly occurs and its influence is considerably reduced or could even vanish. Therefore, low temperature irradiation gives insight on the relative influence of reactive species transport and electronic excitation and charge transport. We found that the effect of lowering the PES irradiation temperature from room temperature to 11 K is small, indicating a minor role for the reactive species transport. Moreover, the two chosen systems allow the examination of the relative magnitude of intra- and intermolecular transfers. We demonstrate that, under conditions where reactive species are almost frozen, intermolecular transfers are very efficient.

Irradiation of ethylene/styrene copolymers: evidence of sensitization of the aromatic moiety as counterpart of the radiation protection effect.

Molecules containing aromatics systems are more stable in the presence of ionizing radiations than alkanes. In the same way, introducing aromatic rings into aliphatic compounds increases their stability. The protective effect is nonlocal and likely results from the transfer of energy and species from the aliphatic moiety to the aromatic one. For years, it was commonly assumed that the aromatic moiety, which is very radiation resistant, accommodates the extra energy remaining unaffected. The use of Fourier transform infrared spectroscopy, online with high energy ion beam irradiation of ethylene/styrene random copolymers, allows us to bring experimental evidence that the benzene rings are sensitized by transfer reactions and consequently that this effect is more important in polymers with low benzene ring molar content.

Irradiation of atactic polystyrene: linear energy transfer effects.

Atactic glassy polystyrene (PS) has been irradiated in anoxic conditions by electron and ion beams. The induced modifications were followed, in situ, by Fourier transform infrared spectroscopy (FTIR). In-film modifications and hydrocarbon gas release were followed. In-situ measurements allowed one to avoid any spurious oxidation of the films after irradiation and also permitted studying in detail the evolution with dose of the FTIR spectra. The data were quantitatively analyzed, and we present a complete analysis of the effects of the Linear Energy Transfer (LET) on the radiation chemical yields of several radiation-induced modifications (alkynes, allenes, alkenes, benzene, and disubstituted benzenes). For a better understanding of the LET effects, the in-film modifications are compared to H2 release data from the literature and to our measurements of hydrocarbon gaseous molecule yields obtained by us. The overall destruction yield becomes very significant at high LET, and the radiation sensitivity of this aromatic polymer merges with typical values of aliphatic polymers: the radiation resistance conferred at low LET to polystyrene by the phenyl side groups is lost at high LET. This loss of radiation resistance equally affects the aromatic and aliphatic moieties. Monosubstituted alkynes are created above a LET threshold, whereas the other radiation-induced modifications are observed in the whole LET range. Several observations indicate that the phenyl ring is broken at high LET. Comparison of the alkyne yield in PS, polyethylene, and polycarbonate as well as the formation of nitrile bonds in poly(vinylpyridine- co-styrene) are consistent with a cleavage of the phenyl ring as the prominent source of alkynes. As the competing damage mechanisms do not have the same LET evolution, the relative importance of a specific modification on the global damage depends on LET. Some (benzene and disubstituted benzenes) dominate at low LET, while others (in-film alkyne and acetylene release) dominate at high LET.