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Eingeladener Vortrag
- nein (985)
Determining a pore structure’s mechanical and chemical data on lime rendering exposed outdoors and including masonry in the laboratory, with regard to their behaviour on moisture transport and weathering was the objective. In search of clues for a dose-response relation - i.e. upon a connection between the emission rate of SO2 and NOx on one hand and the degree of damage to mainly plaster having a lime component on the other - it has been of interest to what extent their structural characteristics including pore space are modified and so consequently also physico-technical properties and chemical composition. For determining corresponding criteria, a widely diversified spectrum of test methods such as to obtain data concerning porosity and moisture transport, mechanical behaviour, and chemistry as well is available. A description of the manufacture of plate-shaped rendering specimens with lime putty, industrially hydrated lime and dolomitic hydrate (the last two also having a cement admixture) and also hydraulic lime as binding agents is included. First deposition velocity and absorption rate for SO2 were determined in laboratory tests on these materials in dry and moist states. After their exposure on outdoor racks at six locations in the Berlin region with differing SO2 atmospheric contents over at least 5 years, the samples of course show timedependent modifications of chemical and physical qualities which are especially reflected in the form of profiles of structure, strength and concentration, e.g. for sulphate. Local climatic differences, however, partly exert a greater influence on material than emissions. Similar investigations were performed on samples of comparable composition exposed 4 and 17 years. But the real surprise is furnished by the renderings’ behaviour depending upon orientation and upon height at a building. Since weathering behaviour and moisture Transport (absorption, storage, release) are directly interdependent, further criteria are necessary for a critical assessment of a plasters’ pore structure. Starting from sands, plasters were characterized. The structural parameters were lastly influenced by the respective contents of sand, binder and mixing water. These results and those gained from bricks naturally find their expression in masonry sections manufactured there from, and above all in their capillary and evaporative behaviours, and also when applying different test liquids. Summary and cited literature is given at the end of this report.
Laser thermal shock experiments - performance and evaluation on the basis of advanced ceramics
(2011)
The thermal shock behaviour in air and vacuum of three different advanced ceramics is investigated by introducing a new testing method. This thermal shock testing system permits the reproducible setting of defined temperature profiles in thin disks. In order to perform heating - up thermal shock experiments under reproducible conditions and to measure the transient temperature fields, a laser beam is directed spirally across the surface of the specimen. In this process, the specimen is heated up faster than the temperature gradient is compensated by thermal conductivity. Resulting temperature fields were recorded space and time resolved. Based on the knowledge of the local temperature distribution at the moment of failure, the critical fracture stress can be calculated. The scatter of thermal shock strength is quantitatively determined for the tested ceramics by using a improved statistical method.
The isotopic composition of boron is a well established tool in various areas of Science and industries. Boron isotope compositions are typically reported as 6"B values which indicate the isotopic difference of a sample relative to the internationally accepted isotope reference material NIST SRM 951. A significant drawback of all of the available boron isotope reference materials is that non covers a natural boron isotope composition apart from NIST SRM 951.
The variation of isotope abundance ratios is increasingly used to unravell natural and technical questions. In the past the investigation and interpretation of such variations was the field of a limited number of experts. With new upcoming techniques and research topics in the last decades, such as provenance and authenticity of food, the number of published isotope data strongly increased. The development of inductively coupled plasma mass spectrometers (ICPMS) from an instrument for simple quantitative analysis to highly sophisticated isotope abundance ratio machines influenced this process significantly. While in former times only experts in mass spectrometry were able to produce reproducible isotope data, nowadays many laboratories, never been in touch with mass spectrometry before, produce isotope data with an ICPMS. Especially for such user isotope reference materials (IRM) are indispensible to enable a reliable method validation. The fast development and the broad availability of ICPMS also lead to an expansion of the classical research areas and new elements are under investigation. Here all users require IRM to correct for mass fractionation or mass discrimination or at least to enable isotope data related to a common accepted basis. Despite this growing interest suitable IRM are still lacking for a number of isotope systems such as magnesium.
Activities for the development of reference materials started as early as 1906 at the US National Bureau of Standards (NBS). In 1912, the first iron and steel reference materials were certified for carbon content in Germany by the Royal Prussian Materials Testing Institute MPA, predecessor of BAM, the Federal Institute for Materials Research and Testing.
Highly energetic silicon tetraazide 1 is synthesized safely in high yield and high purity. The compound is prepared as a solution in benzene which allows it to be handled safely. Stable Lewis base adducts of Si(N3)4 (e.g. 2) are also prepared by treatment of either Si(N3)4 or the disodium salt of hexaazidosilicate (3) with Lewis bases (2,2-bipyridine or 1,10-phenanthroline). Unlike Si(N3)4 the Lewis base adduct 2 is thermally stable and does not decompose below 265 °C. The decomposition is very energetic (ΔHd = -2.4 kJg-1) which means 2 and related Lewis base adducts could replace environmentally harmful Pb(N3)4 used as primary explosive.
Three new offset Delta11B isotope reference materials for environmental boron isotope studies
(2011)
The isotopic composition of boron is a well established tool in various areas of Science and industry. Boron isotope compositions are typically reported as 5nB values which indicate the isotopic difference of a sample relative to the isotope reference material NIST SRM 951.
A significant drawback of all of the available boron isotope reference materials is that none of them covers a natural boron isotope composition apart from NIST SRM 951. To fill this gap of required 5UB reference materials three new solution boric acid reference materials were produced, which cover 6096o of the natural boron isotope Variation (-20 to 40%oo B) of about 100%o. The new reference materials are certified for their B values and are commercially available through European Reference Materials® (http://wwrv.enn-cmi.org). The newly produced and certified boron isotope reference materials will allow straightforward method Validation and quality control of boron isotope data.
The wear behaviour of thin steel wires has been analyzed under oscillating sliding conditions in crossed cylinders contact geometry. The focus of this analysis was the influence of the crossing angle between the wires on the wear. The wires used had 0.45 mm in diameter and the material was cold-drawn eutectoid carbon steel (0.8% C) with a tensile strength higher than 2800 MPa. Two different types of tests were carried out, the first one representing the influence of the crossing angle for a constant load and the second one representing the influence of the crossing angle with constant contact pressure. In the first type of tests it was seen that as the contact angle decreases the contact pressure decreases too and hence less energy specific wear resistance is observed. As a consequence less wear is produced, thus increasing the life of the wires. In the second type of tests it was seen that with constant contact pressure but different crossing angles, nearly the same energy specific wear resistance was observed. This points at an identical wear behaviour in both type of tests but with a running-in and a steady state period as two different wear periods. The tests showed that the running in period may play an important role in the overall wear particle generation and hence the wear occurring in the steady state period is rather mild.
Wear tests are often used in engine development in order to characterize the functional profile of surfaces interacting with lubricants. This paper proposes a new test procedure to determine Stribeck-type curves for the tribosystem piston ring/cylinder liner involving test pieces prepared from engine components. The Variation of the friction coefficient with sliding speed depends on the structure and Constitution of the base oil, the viscosity index, the surface topography of the liner and ring, and the friction modifiers used. Novel organic friction modifiers of low molecular mass not only reduce the friction coefficients under mixed / boundary lubrication, but also in the fluid film regime. In addition, the influence of surface roughness on the wettability of surfaces can be significant for both static and dynamic wetting. For this reason, the interaction of the lubricant with the surfaces was also investigated to enable a correlation between the surface properties of the liquid and solid phases and the tribological behavior.
Original equipment manufacturers (OEMs) and end-users perceive 'Zero Wear' differently. The 'Zero Wear' approach will be put into a general relation for different applications and illuminated by individual paths, either based on monolithic materials, thin film coatings or alternative base oils, featuring triboactive materials and lubricious oxides for tribological engine components and dry running foil bearings or specific DLC, ta-C and novel Zirconium-based thin film coatings for concentrated contacts above FZG 14 and alternative engine oils (NoSAP & bio-no-tox). The associated tribometric test equipments for these examples will also be detailed.
Exclusion from Class 1
(2011)
UN 6(d) Test Results
(2011)
Inspired by the globule arc technique a new electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP OES) method was developed for the analysis of high-purity copper materials. The performance of the method was investigated for the analytes Ag, Al, As, Bi, Cd, Co, Cr, Fe, Mg, Mn, Ni, P, Pb, S, Sb, Se, Si, Sn, Te, Ti, Zn and Zr. ETV parameters were optimized regarding the release of the analytes, the transport efficiency and the quality of analytical results in terms of precision, trueness and power of detection. The influence of CCl2F2, CHClF2, C2H2F4 and CHF3 as gaseous halogenation modifiers was investigated. A sufficient in situ analyte matrix separation was achieved by using CHF3 as halogenating reagent avoiding a high matrix input from the molten copper sample into the ETV system and the plasma. A complete release from the samples was obtained for all investigated analytes except Se and Te. Acceptable results for the determination of the trace elements Ag, Al, As, Bi, Cd, Co, Cr, Fe, Mg, Mn, Ni, P, Pb, S, Sb, Si, Sn, Ti, Zn and Zr in high-purity copper were achieved. The method includes a preceding sample preparation step of oxidizing the surface of copper samples which results in a significantly enhanced sensitivity. In addition to the calibration with copper samples, the feasibility of the calibration with liquid multi-element solutions was investigated. Except for Ag, Mg and Ni all analytes could be analyzed using aqueous calibration solutions. The trueness of the method was tested by the determination of analyte contents of certified reference materials. Limits of quantification ranging from 0.6 ng g-1 to 29 ng g-1 were achieved. The developed direct solid sampling method is time and cost effective and well suited for the characterization of high-purity copper materials. The method can be automated to a large extent and is applicable for processes accompanying analyses. In contrast to all other investigated trace elements, Se and Te were not released from the matrix at measurable levels under the used conditions. The determination of these elements is still under investigation and will be reported in a succeeding publication.