Entwicklungslinien der Schüttgutdosiertechnik

Developments in dosage of bulk solids. Dosage of bulk solids is a fast developing field of process- and production automation. Developments are determined directly by the current demands of the production process, with the properties of the bulk solids and the process itself playing an important role. A survey of proven dosage techniques from the viewpoint of the operating principles, properties, applications, and limitations demonstrates the great variety of problem solutions. An important difference between the individual dosage techniques is the nature and accuracy of mass limitation. The most accurate techniques are the gravimetric dosage methods, with discontinuous weighing giving the greatest accuracy. Developments have been greatly influenced by the state of weighing cell techniques, weighing electronics and computer engineering. The development of measured data acquisition and processing of control, and of instrumentation are described, compared, and assessed. A trend towards system responsibility and development on the part of manufacturers is noted. A accurate dosage of bulk solids requires constant flow of the solids and finely adjustable control devices. The principal interferences in bulk solids flow and measures for their avoidance are shown by means of examples. Successful solution of dosage tasks ultimately requires agreement between manufacturers and processors with regard to definition, determination, and control of dosage accuracy during calibration and during long term operation.     

Organochlorine residues in two seal species from Western Iceland

Harbour seals and grey seals from Faxaflói (Western Iceland) were analyzed for contamination with organochlorines (HCB, PCBs, p,p′-DDT, p,p′-DDE, chlordanes and the enantiomers of α-HCH). Although the values strongly varied, both harbour seals and grey seals on average showed comparable levels of PCBs, p,p′-DDT, p,p′-DDE and α-HCH, as well as chlordanes (ΣCD). Differences were measured in the HCB content of the seal species. The HCB/α-HCH ratio in harbour seals was <1 and in grey seals >1. The results from seals on Iceland were compared with data derived from seal samples of the Antarctic, the Arctic (Spitzbergen) and the North Sea (Germany) in order to give an insight into the global distribution of pollution with chlorinated organics.     

Quantitative vapor-phase infrared spectrometry of ammonia

Reference spectra of ammonia from four sources are compared. Low-resolution spectra (i.e., spectra for which the spectrometer resolution is numerically greater than the full-width at half-height of the rotational lines) were obtained from the Environmental Protection Agency (EPA) web site and from Infrared Analysis, Inc. High-resolution (0.12 cm-1) spectra were obtained from the National Institute for Standards and Technology (NIST) and Pacific Northwest National Laboratory (PNNL). Two protocols were used to validate the EPA and Infrared Analysis spectra, with one requiring that Beer's law be obeyed by the low-resolution spectrum and the other that Beer's law be obeyed by the high-resolution spectrum. In all cases, the second protocol gave a significantly better spectral match. It is shown that the path-integrated concentrations for the low-resolution reference spectra were in error by as little as 4% to as much as an order of magnitude, presumably because of the effect of adsorption on the cell walls. Measured absorptivities of the NIST and PNNL spectra were different by approximately 2.6% and it is believed that the effect of adsorption on these spectra is small. When the same protocols were used to test the reference spectrum of methane, the calculated path-integrated concentration was only approximately 2% different from the one that was calculated from the NIST reference spectrum, suggesting that the data processing protocols provide accurate data.     

Gas chromatography/electron ionization-mass spectrometry-selected ion monitoring screening method for a thorough investigation of polyhalogenated compounds in passive sampler extracts with quadrupole systems

Nontarget analysis and identification of unknown polyhalogenated compounds is important in acquiring a thorough picture of the present pollution status as well as for identifying emerging environmental problems. Such analyses usually require the application of electron ionization mass spectrometry because the resulting mass spectra frequently allow for compound identification. When quadrupoles are used as mass separators, the full scan technique often suffers from low sensitivity along with nonspecificity for polyhalogenated trace compounds which often result in interference by matrix compounds. We have developed a novel nontarget gas chromatography/electron ionization-mass spectrometry-selected ion monitoring (GC/EI-MS-SIM) method that overcomes these sensitivity and selectivity issues. Our method is based on the fact that the molecular ions and isotope patterns of polyhalogenated compounds involve the most relevant primary information with regard to the structure of polyhalogenated compounds. Additionally, the retention times of polyhalogenated compounds generally increase with increasing molecular weight. The retention time range of polyhalogenated compounds was divided in three partly overlapping segments of 112 u (segment A: m/z 300-412; segment B: m/z 350-462; segment C: m/z 450-562) that were screened in eight GC runs consisting of 15 consecutive SIM ions. This method was tested with a passive water sampler extract known to contain over 30 polyhalogenated compounds according to the sensitive analysis by GC/electron capture negative ion (ECNI)-MS. While none of these polyhalogenated compounds could be detected by GC/EI-MS in full scan mode, our nontarget GC/EI-MS-SIM method allowed for the detection of 38 polyhalogenated compounds. Only seven could be identified by means of reference standards while more than 15 of the unknowns could be traced back to at least the class of compounds based on the mass spectrometric data from the nontarget SIM runs. All compounds identified originated from halogenated natural products. The nontarget GC/EI-MS-SIM method combines the high sensitivity obtainable with quadrupole systems for trace analysis with the structural information essential for the identification of unknown pollutants.     

Study on Heat Transfer in Heat Exchangers for a New Supercritical Organic Rankine Cycle

Electrical power from geothermal heat is hardly efficient, if the temperature level of geothermal water is low. This situation is predominant in middle Europe, for example, in Germany, where even in hot-spot areas like Norddeutsches Becken, Oberrheingraben, and Molassebecken the temperature of geothermal water is less than 160°C. For this, efforts have to be made in optimizing the power cycle efficiency. Supercritical fluids provide a higher net energy output per unit mass than subcritical fluids but their physical properties strongly depend on temperature variations, especially close to the supercritical point. Based on the requirements of a new modular and mobile supercritical power cycle MONICA (modular low temperature power cycle Karlsruhe), which will be built within the next few years, different heat exchanger types are investigated within this study in order to determine the most compact design with respect to mobility, mountability, and efficiency. Changes in physical properties of propane, the working fluid of the new cycle, are taken into account by iterative, stepwise calculation of heat exchanger types like double-pipe, shell-and-tube, and plate heat exchangers. For this, common Nusselt number correlations are implemented in the stepwise iteration. Influence of geometry on flow conditions and analysis of part load sensitivity are provided.     

Immunoreactive fraction 1 leaf protein and dry matter content during wilting and ensiling of ryegrass and alfalfa

In four experiments with ryegrass and alfalfa, cut herbage was wilted in the field and silage made in 1- or 200-L silos. Direct-cut (mean DM, 20.3%), low wilt (mean DM, 26.0%), medium wilt (mean DM, 36.2%) and high wilt (mean DM, 47.7%) herbages were used. Fraction 1, the most abundant leaf protein, was measured by crossed immunoelectrophoresis using rabbit anti-Fraction 1 serum. In two ryegrass and one alfalfa experiments in which weather conditions allowed rapid drying to high wilt herbage in 24 h, there was no significant loss of Fraction 1 protein. In the second alfalfa experiment, in which wilting was prolonged to 3 d by adverse weather, there was a 70% loss of Fraction 1. Ensiling proceeded normally in the four experiments, with rapid fall in pH and production of VFA, lactate, and NPN; the extent and rates of production were inversely related to DM content. In alfalfa and ryegrass, pH fell below the isoelectric point of Fraction 1 within 8 d. In each ryegrass experiment, a high proportion (58 to 100%) of Fraction 1 in medium and high wilt silages survived fermentation for 28 and 68 d, with lesser amounts in other silages. With alfalfa, however, almost all Fraction 1 protein was degraded at all DM concentrations during fermentation. Fiber-associated protein increased markedly with increases in DM during wilting, and these differences were present in the mature silage of both ryegrass and alfalfa. Digestibility studies with fistulated sheep showed that appreciable amounts of immunoreactive Fraction 1 protein in ryegrass silages were undegraded in the rumen.     

New interdigital design for large area dye solar modules using a lead‐free glass frit sealing

A new interdigital design for large area dye solar modules is developed for an area of 30×30 cm². This design requires fewer holes in the glass substrate for electrolyte filling, than the conventional strip design. A complete manufacturing process of this module—ranging from screen printed layers to semi‐automated colouring and electrolyte filling—in a laboratory‐scale baseline is illustrated. As primary sealing method, a durable glass frit sealing is used. It is shown, that the lead (Pb) content present in many glass frit powders contaminates the catalytic platinum electrode during the sintering process, resulting in a lowering of the fill factor. A screen printable lead‐free glass frit paste is developed, which solves this problem. Long term stability tests are presented on 2·5 cm² dye solar cells, which have been completely sealed with glass frit. In consecutively performed accelerated ageing tests under 85°C in the dark (about 1400 h) and continuous illumination with visible light (1 sun, about 1700 h), a 2·5 cm² dye solar cell with an electrolyte based on propylmethylimidazolium iodide showed an overall degradation of less than 5% in conversion efficiency. In a subsequently performed thermal cycling test (−40°C to +85°C, 50 cycles) a 2·5 cm² dye solar cell with the same electrolyte composition also showed only a slight degradation of less than 5% in conversion efficiency. Copyright © 2006 John Wiley & Sons, Ltd.