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The present study examines weathering-related degradation mechanisms of CNT-containing polymers and discusses whether and under what conditions degradation might lead to the release of nanoscale components. For this purpose, the study used accelerated artificial aging. The photodegradation of composites based polycarbonate containing multi-walled CNTs of type "Baytubes C150P" was studied under irradiation with a Xenon-arc irradiation device (λ-cut-off at 290 nm).
Resulting surface modifications were evaluated with complementary chemical and microscopic characterization techniques. At sufficiently high radiation dose, a significant degradation of the matrix was observed for some of the polymers under examination which led to entangled networks of uncovered CNT at the composite surface.
By investigation of potential exposure mechanisms of CNTs in polymer composites, the present work contributes to the risk assessment of CNT-containing products.
A process was developed for graphite particle exfoliation in water to stably dispersed multi-layer graphene. It uses electrohydraulic shockwaves and the functionalizing effect of solution plasma discharges in water. The discharges were excited by 100 ns high voltage pulsing of graphite particle chains that bridge an electrode gap. The underwater discharges allow simultaneous exfoliation and chemical functionalization of graphite particles to partially oxidized multi-layer graphene. Exfoliation is caused by shockwaves that result from rapid evaporation of carbon and water to plasma-excited gas species. Depending on discharge energy and locus of ignition, the shockwaves cause stirring, erosion, exfoliation and/or expansion of graphite flakes. The process was optimized to produce long-term stable aqueous dispersions of multi-layer graphene from graphite in a single process step without requiring addition of intercalants, surfactants, binders or special solvents. A setup was developed that allows continuous production of aqueous dispersions of flake size-selected multi-layer graphenes. Due to the well-preserved sp(2)-carbon structure, thin films made from the dispersed graphene exhibited high electrical conductivity. Underwater plasma discharge processing exhibits high innovation potential for morphological and chemical modifications of carbonaceous materials and surfaces, especially for the generation of stable dispersions of two-dimensional, layered materials.
The production of chemically-defined plasma polymers and the introduction of monotype functional groups onto polymer surfaces are described. One method is to lower the energetic level of low-pressure plasmas. Pressure- and plasma-pulsed plasmas were successfully tested for the production of chemically-defined plasma polymers by increasing the monomer supply during the plasma-off period. Well-defined ultra-thin polymer films with regular structure were deposited from atmospheric plasmas by electrospray techniques. Post-plasma wet-chemical processing was also applied, as were gas/liquid-based aerosols and underwater plasmas.