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A thorough characterization of base materials is the prereq- uisite for further research. In this paper, the characterization data of the reference materials (CEM I 42.5 R, limestone pow- der, calcined clay and a mixture of these three components) used in the second funding phase of the priority program 2005 of the German Research Foundation (DFG SPP 2005) are presented under the aspects of chemical and min- eralogical composition as well as physical and chemical properties. The data were collected based on tests performed by up to eleven research groups involved in this cooperative program.
This paper presents the results of an interlaboratory study of the rheological properties of cement paste and ultrasound gel as reference substance. The goal was to quantify the comparability and reproducibility of measurements of the Bingham parameters yield stress and plastic viscosity when measured on one specific paste composition and one particular ultrasound gel in different laboratories using different rheometers and measurement geometries.
The procedures for both in preparing the cement paste and carrying out the rheological measurements on cement paste and ultrasound gel were carefully defined for all of the study’s participants. Different conversion schemes for comparing the results obtained with the different measurement setups are presented here and critically discussed. The procedure proposed in this paper ensured a reasonable comparability of the results with a coefficient of variation for the yield stress of 27% and for the plastic viscosity of 24%, despite the individual measurement series’ having been performed in different labs with different rheometers and measurement geometries.
A thorough characterization of starting materials is the precondition for further research, especially for cement, which contains various phases and presents quite a complex material for fundamental scientific investigation. In the paper at hand, the characterization data of the reference cement CEM I 42.5 R used within the priority program 2005 of the German Research Foundation (DFG SPP 2005) are presented from the aspects of chemical and mineralogical compositions as well as physical and chemical properties. The data were collected based on tests conducted by nine research groups involved in this cooperative program. For all data received, the mean values and the corresponding errors were calculated. The results shall be used for the ongoing research within the priority program.
Two types of cements were selected as the reference cement in the priority program 2005 of the German Research Foundation (DFG SPP 2005). A thorough characterization of CEM I 42.5 R has been made in a recent publication. In this paper, the characterization data of the other reference cement CEM III/A 42.5 N are presented from the aspects of chemical and mineralogical compositions as well as physical and chemical properties. The characterization data of the slag, which is the second main constituent of this specific cement besides the clinker, are presented independently. For all data received, the mean values and the corresponding errors were calculated. The data shall be used for the ongoing research within the priority program. Also, researchers from outside this priority program can benefit from these data if the same materials are used.
Environmental Risk Assessment of Treated Timber in Service - the Environment Focus Group Approach
(2000)
In the context of the Biocidal Products Directive (98/8/EC), and of the OECD work on wood preservatives, the Environment Focus Group (EFG), comprising 8 institutes and the European Wood Preservative Manufacturers Group, has been working on the environmental risk assessment of treated timber in service. A literature review of emissions from treated timber has revealed that very little existing data is usable for environmental risk assessment; the most relevant data are kinetic curves of emissions over time, which show clearly the non-linear emissions behaviour of treated wood over time. The EFG has suggested real exposure conditions for treated timber in the environment, and listed typical exposure scenarios. Five representative scenarios are characterised in detail, for use in the calculation of Predicted Environmental Concentrations (PECs). The existing methods to determine emissions from treated wood have been reviewed. Most existing experimental models cannot be used to predict environmental emissions. Monitoring of commodities in service has its specific constraints. Chemical analysis and ecotoxicity testing have also been reviewed and their relationship has been discussed. Principles for the design of experimental models, for the determination of emission fluxes from treated wood to the environment, have been established.
The present work shows results on elemental distribution analyses in Cu(In,Ga)Se2 thin films for solar cells performed by use of wavelength-dispersive and energy-dispersive X-ray spectrometry (EDX) in a scanning electron microscope, EDX in a transmission electron microscope, X-ray photoelectron, angle-dependent soft X-ray emission, secondary ion-mass (SIMS), time-of-flight SIMS, sputtered neutral mass, glow-discharge optical emission and glow-discharge mass, Auger electron, and Rutherford backscattering spectrometry, by use of scanning Auger electron microscopy, Raman depth profiling, and Raman mapping, as well as by use of elastic recoil detection analysis, grazing-incidence X-ray and electron backscatter diffraction, and grazing-incidence X-ray fluorescence analysis. The Cu(In,Ga)Se2 thin films used for the present comparison were produced during the same identical deposition run and exhibit thicknesses of about 2 µm. The analysis techniques were compared with respect to their spatial and depth resolutions, measuring speeds, availabilities, and detection limits.
Development of a test system for identifying the bitumen type and the modifier used in a reclaimed asphalt Da Polymer-, Gummi-, wachs- und mehrfachmodifizierte Bitumen seit Jahren im Asphaltstraßenbau eigesetzt werden, kommen diese vermehrt im Ausbauasphalt vor. Zur Bewertung des Ausbauasphalts ist es daher notwendig, die Modifizierungen an der Mischanlage zu identifizieren. Die Ausbildung des Bindemittelsacks beim Erweichungspunkt Ring und Kugel ist charakteristisch für die Modifizierung. Hierdurch können wachsmodifizierte Bitumen (WmB) recht präzise und Polymermodifizierten Bitumen (PmB) teilweise identifiziert werden. Mittels Differential Scanning Calorimetry (DSC) werden die Schmelztemperaturen der Wachse erfasst. Hierdurch können WmB identifiziert und die Wachsarten unterschieden werden. Die Analytik mittels Dynamischem Scherrheometer (DSR) startet mit der Bestimmung der Äquisteifigkeitstemperatur EG*T. Bei EG*T werden Frequenz-, Amplituden- und MSCR-Tests durchgeführt. Die Grenze des LVE-Bereichs dient der Identifizierung von WmB. Anhand der Kennwerte bei 0,1 Hz können PmB erkannt werden. Die Rückformung (MSCRT) dient der Identifizierung von Mehrfachmodifizierungen. Da Gummimodifizierte Bitumen (GmB) bei der Extraktion erkannt werden, können alle Modifizierungsarten identifiziert werden. In den FTIR-Spektren (Fourier-Transformations-Infrarotspektroskopie) der modifizierten Bitumen verursachen einige Polymere und Wachse charakteristische Banden, wodurch diese erkannt werden. Die Identifizierung der übrigen Additive erfolgt mithilfe einer multivariaten Auswertung, wodurch mit Ausnahme der GmB (nicht erforderlich) alle Additive erkannt werden. An Stichproben konnte zudem eine Abgrenzung von Mehrfachmodifizierungen sowie eine Abschätzung der Zugabemenge erreicht werden. DSR und FTIR ermöglichen beide eine schnelle, einfache und zielsichere Identifizierung der Bitumenmodifizierungen. Durch die FTIR-Analytik können die Modifizierungen mit der größtmöglichen Präzision bestimmt werden. Die DSR-Analytik erlaubt dafür zusätzlich eine baupraktische Bewertung der Bindemittel.
As polymer, rubber, wax and multi-modified bitumen are used for asphalt road construction since many years, they increasingly occur in reclaimed asphalt. To assess the reclaimed asphalt, it is therefore necessary to identify the modifications in the mixing plants. The formation of the binder bag at softening point ring and ball is characteristic for modification. In this way, wax modified bitumen (WmB) can be identified rather precisely and to a less extent polymer modified bitumen (PmB) can also be identified. Differential scanning calorimetry (DSC) is used to record the melting temperatures of the waxes. In this way, WmB can be identified and a differentiation can be made between the wax types. The analysis by means of the dynamic shear rheometer (DSR) starts with the determination of the equi-stiffness temperature EG*T. Frequency-, amplitude- and MSCR-tests are performed at EG*T. The limit of the LVE range is used to identify WmB. PmB can be identified based on the characteristic values at 0.1 Hz. Creep recovery (MSCRT) is used to identify multi-modifications. As rubber modified bitumen (GmB) is identified on extraction, all types of modification can therefore be identified. Several polymers and waxes cause characteristic bands in the FTIR spectra (Fourier Transform Infrared spectroscopy) of modified bitumen, which enables the identification of these additives. The other additives except the GmB (not necessary) can be identified by means of multivariate model. Further, due to random evaluations, the differentiation between single- and multi-modification as well as the estimation of the content of some additives is possible. DSR and FTIR both enable fast, simple and accurate identification of the bitumen modification. The modification can be determined with the greatest possible precision by using FTIR analysis. On the other hand, DSR analysis allows additional practical assessment of the binder on site.
The 87Sr/86Sr isotope ratio can, in principle, be used for provenancing of cement. However, while commercial cements consist of multiple components, no detailed investigation into their individual 87Sr/86Sr isotope ratios or their influence on the integral 87Sr/86Sr isotope ratio of the resulting cement was conducted previously. Therefore, the present study aimed at determining and comparing the conventional 87Sr/86Sr isotope ratios of a diverse set of Portland cements and their corresponding Portland clinkers, the major component of these cements. Two approaches to remove the additives from the cements, i.e. to measure the conventional 87Sr/86Sr isotopic fingerprint of the clinker only, were tested, namely, treatment with a potassium hydroxide/sucrose solution and sieving on a 11-µm sieve. Dissolution in concentrated hydrochloric acid/nitric acid and in diluted nitric acid was employed to determine the 87Sr/86Sr isotope ratios of the cements and the individual clinkers. The aim was to find the most appropriate sample preparation procedure for cement provenancing, and the selection was realised by comparing the 87Sr/86Sr isotope ratios of differently treated cements with those of the corresponding clinkers. None of the methods to separate the clinkers from the cements proved to be satisfactory. However, it was found that the 87Sr/86Sr isotope ratios of clinker and cement generally corresponded, meaning that the latter can be used as a proxy for the clinker 87Sr/86Sr isotope ratio. Finally, the concentrated hydrochloric acid/nitric acid dissolution method was found to be the most suitable sample preparation method for the cements; it is thus recommended for 87Sr/86Sr isotope analyses for cement provenancing.
Bitumen is a crucial building material in road construction, which is exposed to continuously higher stresses due to higher traffic loads and changing climatic conditions. Therefore, various additives are increasingly being added to the bitumen complicating the characterisation of the bituminous binder, especially concerning the reuse of reclaimed asphalt.
Therefore, this work aimed to demonstrate that the combination of Fourier transform infrared (FTIR) spectroscopy with attenuated total reflexion (ATR) technique and multivariate evaluation is a very wellsuited method to reliable identify and quantify additives in bituminous binders. For this purpose, various unmodified and modified binders, directly and extracted from laboratory and reclaimed asphalts, were investigated with FTIR-ATR spectroscopy. The determined spectra, pre-processed by standard normal variate (SNV) transformation and the determination of the 1st derivation, were evaluated using factor Analysis (FA), linear discriminant analysis (LDA) and partial least square regression (PLSR). With this multivariate evaluation, first, a significant model with a very high hit rate of over 90% was developed allowing for the identification of styrene-butadiene copolymers (SBC), ethylene-copolymer bitumen (ECB) and different waxes (e.g. amide and Fischer-Tropsch wax) even if the additives do not show any additional peaks or the samples are multi-modified. Second, a quantification of the content is possible for SBC, ECB, and Amide wax with a mean error of RMSE B 0.4 wt% and a
coefficient of determination of R2[90%. Based on these results, FTIR identification and quantification of additives in bituminous binders is a very promising method with a great potential.