No abstract

The present study proposed a novel process for the matrix decomposition of carbon-fiber-reinforced plastics (CFRPs). For this purpose, the influence of ultraviolet (UV) radiation paired with semiconductors on CFRP was analyzed. Then, suitable process parameters for superficial and in-depth matrix decomposition in CFRP were evaluated. The epoxy resin was decomposed most effectively without damaging the embedded carbon fiber by using a UV light-emitting diode (LED) spotlight (395 nm, Semray 4103 by Heraeus Noblelight) at a power level of 66% compared to the maximum power of the spotlight. Using a distance of 10 mm and a treatment duration of only 35–40 s achieved a depth of two layers with an area of 750 mm2, which is suitable for technological CFRP repair procedures. In addition to the characterization of the process, the treated CFRP samples were analyzed based on several analytical methods, namely, light microscopy (LM), scanning electron microscopy (SEM), and atomic force microscopy (AFM). Subsequently, the prepared carbon fibers (CFs) were tested using filament tensiometry, single filament tensile tests, and thermogravimetric measurements. All analyses showed the power level of 66% to be superior to the use of 96% power. The gentle (“fiber friendly”) matrix destruction reduced the damage to the surface of the fibers and maintained their properties, such as maximum elongation and maximum tensile strength, at the level of the reference materials.

Cellulose is a renewable and environmentally friendly raw material that has an important economic and technical impact in several applications. Recently, nanocellulose (NC) presented a promising road to support the manufacturing of functional carbon fibers (CFs), which are considered superior materials for several applications because of their outstanding properties. However, the smooth and limited effective surface areas make CFs virtually useless in some applications, such as energy storage. Therefore, strategies to increase the porosity of CFs are highly desirable to realize their potential. Within this article, we present an approach that focuses on the designing of porous CF precursors using polyacrilonitrile (PAN) and NC additives using a wet spinning method. To enhance the porosity, two jet stretching (50% and 100%) and four NC additive amounts (0 wt.%, 0.1 wt.%, 0.4 wt.% and 0.8 wt.%) have been applied and investigated. In comparison with the reference PAN fibers (without NC additives and stretching), the results showed an increase in specific surface area from 10.45 m2/g to 138.53 m2/g and in total pore volume from 0.03 cm3/g to 0.49 cm3/g. On the other hand, mechanical properties have been affected negatively by NC additives and the stretching process. Stabilization and carbonization processes could be applied in a future study to support the production of multifunctional porous CF.

No abstract

The present study investigates the influence of modification temperature and the dose rate of electron modification on the progress of these and the three important thermal induced reactions namely: cyclization, dehydrogenation, and oxidation. Since electron induced chemical reactions strongly depend on the polymer chain segment mobility, temperatures below the glass transition temperature (T g ) and above T g are tested. Electron paramagnetic resonance (EPR) spectroscopy measurements show the presence of alkyl-, peroxy-, and polyimineradicals alongside each other. Gel measurements identified a temperature dependent crosslinking behavior at doses ⩽ 150 kGy, but no dose rate depending on crosslinking. Changes in chemical structure are investigated using Fourier transform infrared spectroscopy (FT-IR), showing a dependency of stabilization behavior depending on dose and temperate more than on dose rate. Thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) measurements complete the analyses by describing the behavior during further thermal treatments and measuring the residual mass at 800 °C.