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The focus of the thesis is to process measurements acquired from a continuous
monitoring system at a railway bridge. Temperature, strain and ambient vibration
records are analysed and two main directions of investigation are pursued.
The first and the most demanding task is to develop processing routines able to extract modal parameters from ambient vibration measurements. For this purpose, reliable experimental models are achieved on the basis of a stochastic system identification(SSI) procedure. A fully automated algorithm based on a three-stage clustering is implemented to perform a modal parameter estimation for every single measurement. After selecting a baseline of modal parameters, the evolution of eigenfrequencies is
studied and correlated to environmental and operational factors.
The second aspect deals with the structural response to passing trains. Corresponding
triggered records of strain and temperature are processed and their assessment is
accomplished using the average strains induced by each train as the reference parameter.
Three influences due to speed, temperature and loads are distinguished and treated individually. An attempt to estimate the maximum response variation due to each factor is also carried out.
In this paper we introduce LUCI, a Lightweight Urban Calculation Interchange system, designed to bring the advantages of a calculation and content co-ordination system to small planning and design groups by the means of an open source middle-ware. The middle-ware focuses on problems typical to urban planning and therefore features a geo-data repository as well as a job runtime administration, to coordinate simulation models and its multiple views. The described system architecture is accompanied by two exemplary use cases that have been used to test and further develop our concepts and implementations.
Data acquisition systems and methods to capture high-resolution images or reconstruct 3D point clouds of existing structures are an effective way to document their as-is condition. These methods enable a detailed analysis of building surfaces, providing precise 3D representations. However, for the condition assessment and documentation, damages are mainly annotated in 2D representations, such as images, orthophotos, or technical drawings, which do not allow for the application of a 3D workflow or automated comparisons of multitemporal datasets. In the available software for building heritage data management and analysis, a wide range of annotation and evaluation functions are available, but they also lack integrated post-processing methods and systematic workflows. The article presents novel methods developed to facilitate such automated 3D workflows and validates them on a small historic church building in Thuringia, Germany. Post-processing steps using photogrammetric 3D reconstruction data along with imagery were implemented, which show the possibilities of integrating 2D annotations into 3D documentations. Further, the application of voxel-based methods on the dataset enables the evaluation of geometrical changes of multitemporal annotations in different states and the assignment to elements of scans or building models. The proposed workflow also highlights the potential of these methods for condition assessment and planning of restoration work, as well as the possibility to represent the analysis results in standardised building model formats.
The world society faces a huge challenge to implement the human right of “access to sanitation”. More and more it is accepted that the conventional approach towards providing sanitation services is not suitable to solve this problem. This dissertation examines the possibility to enhance “access to sanitation” for people who are living in areas with underdeveloped water and wastewater infrastructure systems. The idea hereby is to follow an integrated approach for sanitation, which allows for a mutual completion of existing infrastructure with resource-based sanitation systems.
The notion “integrated sanitation system (iSaS)” is defined in this work and guiding principles for iSaS are formulated. Further on the implementation of iSaS is assessed at the example of a case study in the city of Darkhan in Mongolia. More than half of Mongolia’s population live in settlements where yurts (tents of Nomadic people) are predominant. In these settlements (or “ger areas”) sanitation systems are not existent and the hygienic situation is precarious.
An iSaS has been developed for the ger areas in Darkhan and tested over more than two years. Further on a software-based model has been developed with the goal to describe and assess different variations of the iSaS. The results of the assessment of material-flows, monetary-flows and communication-flows within the iSaS are presented in this dissertation. The iSaS model is adaptable and transferable to the socio-economic conditions in other regions and climate zones.
The development of a hydro-mechanically coupled Coupled-Eulerian–Lagrangian (CEL) method and its application to the back-analysisof vibratory pile driving model tests in water-saturated sand is presented. The predicted pile penetration using this approachis in good agreement with the results of the model tests as well as with fully Lagrangian simulations. In terms of pore water pressure, however, the results of the CEL simulation show a slightly worse accordance with the model tests compared to the Lagrangian simulation. Some shortcomings of the hydro-mechanically coupled CEL method in case of frictional contact problems and pore fluids with high bulk modulus are discussed. Lastly, the CEL method is applied to the simulation of vibratory driving of open-profile piles under partially drained conditions to study installation-induced changes in the soil state. It is concluded that the proposed method is capable of realistically reproducing the most important mechanisms in the soil during the driving process despite its addressed shortcomings.
Die Arbeit leistet einen wissenschaftlichen Beitrag zur Erforschung der Einsatzmöglichkeiten eines Immobilienportfoliomanagements für öffentliche museale Schlösserverwaltungen in Deutschland. Insbesondere wird ein für deren Organisation spezifisches Modell zur Investitionssteuerung herausgearbeitet und dessen Anwendbarkeit in der Praxis mit Experten diskutiert.
Der Einsatz ungeeigneter Materialien ist eine der häufigsten Ursachen für Bauwerksschäden. Da die Beseitigung dieser Schäden oft mit hohen Kosten verbunden ist, besteht in der Baupraxis der Bedarf an einer Identifizierungsmethode für eingesetzte Baustoffe. Daneben wäre eine Kenntnis der in einem Bauwerk vorliegenden Materialien auch für Instandhaltungsarbeiten hilfreich.
Die Identifizierung der in einem Festbeton oder Festmörtel vorliegenden Zementart gilt auch gegenwärtig noch als schwierig oder sogar unmöglich. Die Schwierigkeiten ergeben sich in erste Linie daraus, dass die Hydratationsprodukte verschiedener Zementarten oft nur geringe Unterschiede in ihrer chemischen und mineralogischen Zusammensetzung aufweisen und die Hydratationsmechanismen bei einigen Zementarten noch nicht vollständig erforscht sind.
Primäres Ziel der vorliegenden Arbeit war es zu untersuchen, ob anhand des Mineralphasenbestandes, der sich während einer thermischen Behandlung von Zementsteinen einstellt, eine Identifizierung der vorliegenden Zementart möglich ist. Weiterhin sollte die Übertragbarkeit dieser Ergebnisse auf Betone und Mörtel eingeschätzt werden.
Zur Schaffung von Identifizierungsmerkmalen wurden die (angereicherten) Zementsteine bei Temperaturen im Bereich zwischen 600 °C und 1400 °C thermisch behandelt. An den getemperten Proben wurde der Mineralphasenbestand mittels Röntgendiffraktometrie bestimmt. Mit der gleichen Methode wurden die Ausgangszemente und die (angereicherten) Zementsteine untersucht. Aus der Gegenüberstellung der nachgewiesenen Mineralphasen konnten die gesuchten Identifizierungsmerkmale abgeleitet werden. Um den Einfluss der Gesteinskörnungen auf die Identifizierungsmöglichkeiten gesondert zu erfassen, wurde das Versuchsprogramm auf 3 Abstraktionsebenen angelegt. Für die Auswertung der Ergebnisse wurden die Proben zu Klassen zusammengefasst, welche jeweils charakteristische Zusammensetzungen der Ausgangszemente repräsentieren. Für die Analyseergebnisse wurden die klassenspezifischen die Mittel- und Grenzwerte bestimmt.
Als die effektivste Methode zur Anreicherung der Zementsteinmatrix aus Mörtel- und Betonproben erwies sich die Kombination aus einer Zerkleinerung in einem Laborbackenbrecher. Die fein partikulären Fraktionen, welche Zementsteingehalte von 70-80 Ma.-% aufwiesen, wurden als Analyseproben verwendet. Es zeigte sich aber auch, dass das Anreicherungsergebnis von der Gesteinskörnungsart abhängt. Bei Laborbetonen mit einer Kalkstein-Gesteinskörnung wurde mit der gleichen Methode lediglich eine Anreicherung des Zementsteins auf etwa 50 Ma.-% erreicht.
Die Untersuchungen auf Abstraktionsebene 1 lieferten die Erkenntnis, dass der Hydratationsprozess der Klinkerphasen, der Klinkerphasengemische sowie des Hüttensandes, auch in Gegenwart des Sulfatträgers für Behandlungstemperaturen im Bereich des Klinkerbrandes vollständig reversibel ist. Im Hinblick auf die Identifizierungsmöglichkeiten wurde 1100 °C als optimale Behandlungstemperatur ermittelt, da hier eine Schmelzphasenbildung ausgeschlossen werden kann.
Durch eine Gegenüberstellung der chemischen Zusammensetzung der Ausgangszemente und des Phasenbestandes nach der Temperung konnte nachgewiesen werden, dass bei reinen Zementsteinen grundsätzlich alle Bestandteile an der Reaktion, die während der thermischen Behandlung bei 1100 °C stattfindet, beteiligt sind. Der sich einstellende Phasen bestand ist nur von der chemischen Zusammensetzung der Probe und dabei besonders von derem CaO-Gehalt abhängig. Empirisch wurde eine Prioritätenfolge für die Phasenbildung ermittelt. Daraus geht hervor, dass bevorzugt CaO-reiche Phasen, wie Aluminatferritphase, Belit und Ye‘elimit entstehen und dass überschüssiger Kalk als freies CaO vorliegt. Nur wenn der CaO-Gehalt der Probe nicht für die vollständige Bildung der – in der Summe – kalkreichsten Phasen ausreicht, entstehen partiell oder vollständig kalkärmere Phasen, wie Merwinit und Melilith. Basierend auf den Prioritäten zur Phasenbildung wurde ein Satz von Berechnungsgleichungen aufgestellt, mit denen der CaO-Typ aus der Phasenzusammensetzung der bei 1100 °C getemperten Probe bestimmt werden kann. CaO-Typen repräsentieren Bereiche für die chemische Zusammensetzung der Ausgangsprobe, welche bei der Temperaturbehandlung zu einer charakteristischen qualitativen Phasenzusammensetzung führen. Die CaO-Typen der marktüblichen Zementarten wurden anhand der in der Norm EN 197 festgelegten Bereiche für die Zusammensetzung der Zemente aus ihren Hauptbestandteilen sowie der aus der Fachliteratur ermittelten Bereiche für die chemische Zusammensetzung dieser Hauptbestandteile ermittelt. Damit kann für die Zementarten der Phasenbestand vorhergesagt werden, welcher sich während der Temperaturbehandlung des entsprechenden Zementsteins einstellt. Ein Vergleich mit dem gemessenen Phasenbestand erlaubt so die Identifizierung der Zementart.
Die Übertragbarkeit der durch die Untersuchungen an den Zementsteinen gewonnenen Erkenntnisse und die daraus abgeleiteten Identifizierungsmöglichkeiten auf Zementsteine, welche aus quarzsandhaltigen Normmörteln angereichert wurden, konnte nachgewiesen werden. Dabei wurde eine leichte Verschiebung des Phasenbestandes hin zu kalkärmeren Phasen beobachtet, welche auf die Reaktionsbeteiligung eines Teils der in den Proben enthaltenen Restgesteinskörnung zurückzuführen ist. Die Unterscheidungsmöglichkeiten zwischen den Zementarten blieben jedoch überwiegend erhalten.
Bei Betonen nimmt der Einfluss der Gesteinskörnung auf den Phasenbestand deutlich zu und kann zum Teil nicht mehr vernachlässigt werden. Die Identifizierungsmöglichkeiten müssen deshalb nach der chemischen Zusammensetzung und der Reaktivität der Gesteinskörnung differenziert ermittelt werden. Dazu sind weitere Untersuchungen notwendig.
Für Zementsteine, zementsteinreiche Systeme sowie Mörtel und Betone mit wenig reaktiven Gesteinskörnungen kann die Zementart bereits mit der in dieser Arbeit vorgestellten Methode identifiziert werden. In Fällen, für die sich die Bereiche der chemischen Zusammensetzung mehrerer Zementarten überschneiden, kann es dabei notwendig sein, zusätzliche chemische bzw. mineralogische Untersuchungen durchzuführen, z. B. am unbehandelten Zementstein.
Superplasticizers are utilized both to improve the fluidity during the placement and to reduce the water content of concretes. Both effects have also an impact on the properties of the hardened concrete. As a side effect the presence of superplasticizers affects the strength development of concretes that is strongly retarded. This may lead to an ecomomical drawback of the concrete manufacturing. The present work is aimed at gaining insights on the causes of the retarding effect of superplasticizers on the hydration of Portland cement. In order to simplify the complex interactions occurring during the hydration of Portland cement the majority of the work focuses on the interaction of superplasticizer and tricalcium silicate (Ca3SiO5 or C3S, the main compound of Portland cement clinker). The tests are performed in three main parts accompanied by methods as for example isothermal conduction calorimetry, electrical conductivity, Electron Microscopy, ICP-OES, TOC, as well as Analytical Ultracentrifugation.
In the first main part and based on the interaction of cations and anionic charges of polymers, the interactions between calcium ions and superplasticizers are investigated. As a main effect calcium ions are complexed by the functional groups of the polymers (carboxy, sulfonic). Calcium ions may be both dissolved in the aqueous phase and a constitute of particle interfaces. Besides these effects it is furthermore shown that superplasticizers induce the formation of nanoscaled particles which are dispersed in the aqueous phase (cluster formation). Analogous to recent findings in the field of biomineralization, it is reasonable to assume that these nanoparticles influence the crystal growth by their assembly process.
Based on the assumption that superplasticizers hinder either or both dissolution and precipitation and by that retard the cement hydration, the impact on separate reactions is investigated. On experiments that address the solubility of C-S-H phases and portlandite, it is shown that complexation of calcium ions in the aqueous phase by functional groups of polymers increases the solubility of portlandite. Contrary, in case of C-S-H solubility the complexation of calcium ions in solution leads to decrease of the calcium ion concentration in the aqueous phase. These effects are explained by differences in adsorption of polymers on C-S-H phases and portlandite. It is proposed that adsorption is stronger on C-S-H phases compared to portlandite due to the increased specific surface area of C-S-H phases. Following that, it is claimed that before polymers are able to adsorb on C-S-H phases the functional groups must be screened by calcium ions in the aqueous phase. It is further shown that data regarding the impact of superplasticizers on the unconstrained dissolution rate of C3S does not provide a clear relation to the overall retarding effect occurring during the hydration of C3S. Both increased and decreased dissolution rate with respect to the reference sample are detected. If the complexation capability of the superplasticizers is considered then also a reduced dissolution rate of C3S is determined. Despite the fact that the global hydration process is accelerated, the addition of calcite leads to a slower dissolution rate. Thus, a hindered unconstrained dissolution of C3S as possibly cause for the retarding effect still remains open for discussion. In the last section of this part, the pure crystallization of hydrate phases (C-S-H phases, portlandite) is fathomed. Results clearly show that superplasticizers prolong the induction time and modify the rate of crystal growth during pure crystallization in particular due to the complexation of ions in solution. But this effect is insufficient to account for the overall retarding effect. Further important factors are the blocking of crystal growth faces by adsorbed polymers and the dispersion of nanoscaled particles which hinders their agglomeration in order to build up crystals.
In the last main part of the work, the previously gathered results are utilized in order to investigate hydration kinetics. During hydration, dissolution and precipitation occur in parallel. Thereby, special attention is laid on the ion composition of the aqueous phase of C3S pastes and suspensions in order to determine the rate limiting step. All in all it is concluded that the retarding effect of superplasticizers on the hydration of tricalcium silicate is based on the retardation of crystallization of hydrate phases (C-S-H phases and portlandite). Thereby, the two effects complexation of calcium ions on surfaces and stabilization of nanoscaled particles are of major importance. These mechanisms may partly be compensated by template performance and increase in solubility by complexation of ions in solution. The decreased dissolution rate of C3S by the presence of superplasticizers during the in parallel occuring hydration process can only be assessed indirectly by means of the development of the ion concentrations in the aqueous phase (reaction path). Whether this observation is the cause or the consequence within the dissolution-precipitation process and therefore accounts for the retarding effect remains a topic for further investigations.
Besides these results it is shown that superplasticizers can be associated chemically with inhibitors because they reduce the frequency factor to end the induction period. Because the activation energy is widely unaffected it is shown that the basic reaction mechanism sustain. Furthermore, a method was developed which permits for the first time the determination of ion concentrations in the aqueous phase of C3S pastes in-situ. It is shown that during the C3S hydration the ion concentration in the aqueous phase is developed correspondingly to the heat release rate (calorimetry). The method permits the differentiation of the acceleration period in three stages. It is emphasized that crystallization of the product phases of C3S hydration, namely C-S-H phases and portlandite, are responsible for the end of the induction period.
Components of structural glazing have to meet different requirements and resist various impacts, depending on the field of application. Within an international research project of the EU innovation program Horizon 2020, special glass panes with a fluid circulating in capillaries are developed exploiting solar energy. Major influences to this glazing are UV irradiation and the fluidic contact, effecting the mechanical and optical durability of the bonding material within the glass setup. Regarding to visual requirements, acrylate adhesives and EVA films are analyzed as possible bonding materials by destructive and non-destructive testing methods. Two types of specimen are presented for obtaining the mechanical behavior and the surface appearances of the bonding material.
As part of an international research project – funded by the European Union – capillary glasses for facades are being developed exploiting storage energy by means of fluids flowing through the capillaries. To meet highest visual demands, acrylate adhesives and EVA films are tested as possible bonding materials for the glass setup. Especially non-destructive methods (visual analysis, analysis of birefringent properties and computed tomographic data) are applied to evaluate failure patterns as well as the long-term behavior considering climatic influences. The experimental investigations are presented after different loading periods, providing information of failure developments. In addition, detailed information and scientific findings on the application of computed tomographic analyses are presented.