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The net section limit load FY is a key input parameter for the accuracy of any
elastic-plastic flaw assessment procedure of the R6 type. Unfortunately available limit load
solutions are of variable quality since they have been obtained over decades by different
methods. As a consequence the results of the fracture analyses such as the critical load or
crack size are limited in their accuracy and are often significantly conservative. A further
problem is that common limit load solutions based on ligament yielding are inadequate in a
number of cases even for through crack configurations and should be replaced by some
kind of local yielding solutions. In the present paper a simple and straightforward reference
load definition is proposed instead of the limit load which strictly corresponds to a ligament
yielding parameter Lr = 1 in the R6 Routine and similar approaches such as SINTAP and
FITNET. This can be determined by finite element simulation for any geometry. In addition to
a previous study on thin wall notched plates the method is applied to plates containing
shallow semi-elliptical surface cracks. The results demonstrate that the approach provides a
suitable extension and improvement of the existing methods.
Abstract Hydrogenated nitrile butadiene rubber (HNBR) elastomer was thermo-oxidatively aged at different temperatures up to 150 °C. Fourier transform infrared spectroscopy (FTIR), compression stress relaxation (CSR) and international rubber hardness degree (IRHD) microhardness were used to characterise the chemo-mechanical changes of HNBR O-rings during thermo-oxidative ageing. FTIR shows the development of carbonyl, methyl and ester groups but the nitrile content was not affected by ageing. The effect of sample geometry during CSR was investigated. CSR data were converted through integrated kinetic laws. The conversion has proven its sensibility to detect heterogeneous ageing. This was confirmed by the IRHD measure-ments across the section of O-rings. The influence of compression during ageing was assessed through IRHD measurements across the section of compressed and uncom-pressed aged O-rings. The DLO effect was more pronounced in compressed O-rings. By applying the model of Wise et al., theoretical IRHD and oxidation profiles were determined on the basis of IRHD experimental data of compressed O-rings. Good agreements between the experimental and the theoretical IRHD profiles in the core region were obtained. However, near the edge, the theoretical IRHD values were overestimated.
The glass transition behavior of ultra-thin supported polymer films is discussed controversially in the literature for around 20 years. Substantial efforts have been archived to understand it. In this contribution, a combination of methods sensitive to bulk properties of a system, like dielectric or specific heat spectroscopy with surface analytics, for instance, atomic force microscopy (AFM), contact angle measurements, and X-ray photoelectron spectroscopy (XPS) were employed to study the glass transition of ultra-thin supported films. All investigations were carried out on identically prepared and treated samples. Different systems with different complexities going from more or less flexible homopolymers over rigid main chain macromolecules to polymer blends have been studied. For the investigated flexible macromolecules, the dynamic glass transition temperature estimated within the frame of the linear response approach is independent of the film thickness down to several nanometers and identical to the bulk value. For polystyrene it was found the thermal glass transition temperatures can depend on the film thickness. This different behavior is not well understood till now and needs further experimental clarification. For the investigated main chain polymers polycarbonate and polysulfone. Dynamic and thermal glass transition temperature estimated from the dielectric measurements increases with decreasing film thickness. This is discussed in the frame of a strong interaction of the polymer segments with the surface of the substrate. In general for homopolymers, the interaction energy of the polymer segments with the substrate surface cannot be considered as the only parameter, which is responsible for the change in the thermal glass transition with the film thickness. For the investigated miscible blend system of polystyrene/poly(vinyl methyl ether) at a composition of 50/50 wt-% a decrease of the dynamic glass transition temperature with decreasing film thickness is found. This is explained by the formation of a poly(vinyl methyl ether)-rich surface layer with a higher molecular mobility.
Within the project COORAL (German acronym for 'CO2 purity for capture and storage') first studies on piping steels exposed to CO2 and artificial brine with high chloride concentration have been carried out. Corrosion behavior of martensitic Cr13 steel (1.4034) was investigated in a corrosive environment (artificial saline brine, T = 60 °C, CO2-flow rate 3 – 5 L/h, atmospheric pressure, exposure times from 1 h up to 14 days) using electrochemical and metallographic techniques. Different corrosion kinetics were observed as a function of exposure times and chloride concentration in the artificial brine. In CO2-saturated brine pitting corrosion was observed at free corrosion potential, whereas in the brine without addition of NaCl a stable passive layer built up. Predictions about corrosion mechanism are made and verified by means of surface analytical techniques.