Anteil erneuerbarer Energien und klimarelevante CO2-Emissionen aus der thermischen Verwertung von Abfällen in Österreich

Since combustible wastes usually consist of biogenic (e.g. paper, wood, food waste) and fossil organic matter (plastics), their thermal recovery results in climate neutral and climate relevant CO₂ emissions. Moreover, the fraction of biogenic materials in the waste feed is relevant for the amount of renewable energy produced. The latter has to be reported and might be subsidized according to national laws (e.g. based on European directive 2009/28/EG). The present study represents the first comprehensive evaluation of the share of biogenic and fossil materials in the waste feed of waste-to-energy (WTE) plants on a national basis. The Balance Method, which is patented on a European level by TU Wien, was applied to 10 out of 13 Austrian WTE plants (around 2.3 Mio tons of waste corresponding to around 88 % of the overall waste feed in Austrian WTE plants). The method is based on the mathematical reconciliation of the material properties (e.g. mean chemical composition of biogenic and fossil materials) and routinely recorded operating data of WTE plants (e.g. flue gas volume, CO₂ and O₂-content in the dry flue gas, steam production). The results demonstrate large variations for the share of energy from biogenic sources in the different WTE plants, ranging from 35.7 ± 2.4 % to 61.2 ± 2.7 % (based on annual averages). Additionally, for several WTE plants large temporal variations can be observed based on monthly mean values. Thus, a plant-specific and continuous evaluation of the waste composition in WTE plants (which the Balance Method allows to do at reasonable efforts) can be recommended for a reliable reporting of the renewable share of energy or fossil CO₂ emissions from waste incineration. The energy input which stems from fossil and biogenic sources can be estimated to 11,450 ± 120 TJ and 10,730 ± 110 TJ, respectively for the year 2014 (for the 10 WTE plants). In total 1060 ± 24 kt fossil CO₂ emissions from the thermal recovery of waste in Austria’s WTE plants in 2014 could be determined (estimation for all 13 WTE plants).     

Determination of nano-roughness of carbon fibers by atomic force microscopy

We present a novel approach to determine the surface roughness on varying scales using atomic force microscopy data. The key factor is to find a suitable background correction for the desired scale. Using the example of the surface of sized and unsized high-tenacity carbon fibers, we present an easy method to find backgrounds for widely varying scales and to evaluate respective topography and surface roughness with the same lateral resolution as the microscope itself. The analysis is done by subtracting a tunable background from the respective height data. By choosing an appropriate background to investigate the surface topography of a carbon fiber on a nm-scale, only small nano-structures with a width of around 20 nm remain after the background subtraction. Evaluating the mean roughness R _a of these nano-structures, sized carbon fibers show an overall value of around 0.1 nm while unsized carbon fibers a value of around 0.4 nm. Total background corrected height analysis shows an even distribution of these nano-structures along the fibrils of the unsized fibers, whereas for the sized fibers the nano-structures are not present. The presented method allows analysis and visualization of the distribution of nano-structures on a carbon fiber surface for the first time. This feature is used to visualize the distribution of the sizing and can further be used to investigate the influence of different production parameters on the fiber topography or to evaluate the contribution of mechanical interlocking to the interfacial strength.     

Cu/Ni‐Loaded CeO2‐ZrO2 Catalyst for the Water‐Gas Shift Reaction: Effects of Loaded Metals and CeO2 Addition

Two different types of metals (Cu and Ni) and the effect of CeO₂ addition to produce a CeO₂‐ZrO₂ co‐supporter were investigated through the water‐gas shift (WGS) reaction. It was found that the WGS activity could be enhanced with CeO₂ addition. At relatively high temperature, Ni‐loaded catalysts exhibited higher CO conversion while Cu‐loaded catalysts demonstrated better performance at low temperatures. The stability and yield of the CO₂ and H₂ products of the Cu catalysts were higher than those of the Ni catalysts. These results may be caused by an irreversible adsorption of CO on Ni and the reverse WGS reaction occurring on the Ni catalysts. In situ diffuse‐reflection infrared Fourier transform spectroscopy data suggests that the WGS mechanism likely proceeded via formate species.     

Archaeological Arsenical Bronzes and Equilibrium in the As-Cu System

Metallurgical and Materials Transactions B - Understanding the effects of impurities, segregation, undercooling, and solidification velocity is necessary to reconstruct prehistoric As-Cu alloy...     

Influence of architecture on the Raman spectra of acid-treated carbon nanostructures

Raman spectroscopy was used to characterise 11 varieties of carbon nanostructures (CNSs) consisting on seven varieties of commercial multi-walled carbon nanotubes, two types of carbon nanofibres and two types of lab-synthesised single-walled carbon nanotubes. The Raman spectra of these CNSs provided information on the structural ordering of the as-received (or as-synthesised) material. Additionally, the CNSs were chemically treated by two mixtures of nitric and sulphuric acids at markedly different concentrations and then characterised by Raman spectroscopy. The features of the G and D Raman bands of the CNSs were used to assess structural modifications and generation of defects induced by the acid treatments. Changes in the Raman spectra before and after acidic treatment depend strongly on the initial intensity ratio of the G to D bands and the architecture (number of layers or diameter) of the CNSs.     

Comparative characterization of chip to epoxy interfaces by molecular modeling and contact angle determination

An investigation of interfacial interaction has been performed between three epoxy molding compound materials and a native silicon dioxide layer (SiO₂) usually found at chip surfaces. The epoxy materials were an industry oriented epoxy molding compound Epoxy Phenol Novolac (EPN), its filled variety EPN^F (with silica particles) and a model aromatic epoxy¹ (2 1 2). All systems are described in full in [1] and [2]. The free surfaces of the solid materials were experimentally analyzed by contact angle measurements of three different liquids (water, methylene-iodide (MI) and glycerol). Results are compared to interfacial energies obtained by analysis of the interfaces in bimaterial molecular models, yielding reasonable agreement. A qualitative prediction regarding the influence of water on the interfacial strength between chip and molding compound is attempted.