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- Rheology (23)
- Cement (20)
- Concrete (13)
- Superplasticizer (7)
- Cement hydration (6)
- Polycarboxylate ether (6)
- Self-compacting concrete (6)
- Admixtures (5)
- Polysaccharides (5)
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In this paper, we demonstrate the value of 1H NMR relaxometry for studying the hydration of clinker-reduced, more climate-friendly cementitious binders. The results were obtained on typical CEM I cements and sister samples containing two different reactive agricultural ashes as well as non-reactive biochars as supplementary cementitious materials. The findings prove that time-resolved NMR measurements provide valuable additional information when combined with classical heat flow calorimetry.
Polymers that help tailoring rheological properties during the casting process have become inevitable constituents for all kinds of high-performance concrete technologies. Due to lacking industries, these typically crude-oil based admixtures are not readily available in many parts of the world, which limits the implementation of more sustainable high-performance construction technologies in these regions. Alternative polymers, which often demand for less processing, can be derived from local plant-based resources. The paper provides experimental data of flow tests of cement pastes with polysaccharides from Triumfetta pendrata A. Rich, acacia gum and cassava without and in the presence of polycarboxylate ether superplasticizer. The flow tests are amended by observations of the zeta potentials and the hydrodynamic diameters in the presence of and without calcium ions in the dispersion medium. The results show that in the presence of and without calcium ions all polysaccharides provide negative zeta potentials, yet, they affect flowability and thixotropy in different ways. Cassava starch, acacia gum, and the gum of Triumfetta pendrata A. Rich qualified well for robustness improvement, strong stiffening, and additive manufacturing, respectively. The reason for the different effects can be found in their average sizes and size distribution. Due to the promising results, a flow chart for local value chains is derived on the example of yet unused cassava wastes, which can be converted in parallel.
Synopsis: The paper presents the results of a study on the influence of agitation on the structural build-up of fresh cement pastes using a penetration test. It first presents results about the influence of the penetrating shape’s geometry on the influence on the cement paste specimen. Then, results are shown for the load-deflection curves depending upon time and agitation before testing. Based on the observation of the force required to penetrate the sample, conclusions on the structural build-up can be made. The observations were made over the course of time with samples that were left at rest and partly agitated before testing at different time steps. The setup allows to identify the contribution of the chemical reaction to the structural build-up process. The presence of superplasticizer obviously reduces the load that cement paste can withstand, while the loss of thixotropy is found notably lower than that of neat cement pates
Synopsis: Lately, there has been rising attention to superplasticizers (SP) based on polyphosphate esters. However, the influence of the molecular structure of the polyphosphate polymers on time-dependent properties such as structural build-up has not been examined yet intensively. To investigate this effect, three comb polyphosphate superplasticizers with different charge densities were synthesised by free radical polymerisation. Our findings indicate that SP with the lowest and medium charge densities extend the induction period more strongly than the SP with the highest charge density. The reduction of the structural build-up rate is linearly dependent on the dosage and concentration of the functional group of polyphosphate SP in the cementitious system. This study proposes a mathematical equation expressing the relationship between the structural build-up rate during the induction period and the molecular structure of the polyphosphate SP.
Influence of the hydroxypropylation of starch on its performance as viscosity modifying agent
(2022)
Synopsis: Starch is a commonly used viscosity modifying agent (VMA). The performance of starch as VMA depends on its origin (e.g. potato, corn, cassava, etc.) and corresponding molecular properties, such as molecular weight, ratio between amylose and amylopectin etc. Depending upon the application, the efficiency of starch can be enhanced by hydroxypropylation. The maximum degree of substitution (DoS) cannot be greater than 3.0, which is the number of hydroxy groups per glucose monomer in the polymer. In the current research three potato starches exhibiting the DoS of 0.4, 0.6 and 0.8 were utilised. The influence of the modified starch on the rheological properties and hydration of cement paste, as well as the viscosity of the pore solution were investigated. Our findings show that the starch with the highest DoS increases the dynamic yield stress the most, while the plastic viscosity is less dependent on the DoS. Additionally, starch with the highest DoS retards hydration to lower degree than other starches.
Organic/inorganic mixtures were prepared from ordinary Portland cement (OPC), water (w/c 0.22), a fluorescent dye in aqueous solution (stable at alkaline pH; BAM-I), and two different comb shape polycarboxylates (PCEs), i.e., high charge (PCE-HC) and low charge (PCE-LC), respectively. Rheological and calorimetric measurements were performed prior to optical studies in order to select PCE concentrations. Absorption and fluorescence spectroscopy of the system OPC + BAM-I (CBAM-I) revealed maxima of dye BAM-I located at 645 nm and 663 nm, respectively. In presence of PCE-HC and PCE-LC, these mixtures displayed a small red shift in reflectance and a faster decrease in intensity compared to studies with CBAM-I; however, only slight differences were observed between the different PCEs. With time, all systems exhibited a decrease in intensity of BAM-I in absorption/reflectance and emission. This could be caused by dye adsorption and possibly decomposition when in contact with cement particles or hydration products.
The presence of polycarboxylate ether (PCE) based superplasticizers (SPs) has enormous influence on the early hydration of cement. C3A as the most reactive phase of Portland cement plays a significant role in early hydration reactions and affects the rheological performance. Therefore, this paper presents experimental results about the influence of delayed addition of PCEs on the Hydration of cement and C3A-gypsum pastes investigated by isothermal heat flow calorimetry. Complementary in-situ XRD was carried out on C3A pastes to analyze hydration and phase changes related to the addition of PCE.
Cement pastes with a delayed addition of PCE showed less Retardation compared to simultaneous addition. The alteration caused by PCE is much more pronounced for C3A-gypsum mixes. With a delayed addition of SP, the hydration of C3A is less retarded or even accelerated. It is obvious that there is less retardation the later the addition of SP. Furthermore, the PCE alter the hydration of C3A when added delayed and exhibit changes in kinetics and hydration rates. XRD results showed that more C3A is dissolved in the presence of PCE. Also, the gypsum depletion occurs earlier in the presence of PCE and even faster with delayed addition. Without PCE AFm starts to form just after the gypsum depletion. However, in the presence of PCE AFm already starts to form at the beginning of the hydration. Due to the faster gypsum depletion in the presence of PCE, also the transformation from ettringite into AFm begins earlier, but takes longer as without SP.
The presence of polycarboxylate ether (PCE) based superplasticizers (SPs) has an enormous influence on the early hydration of cement. The hydration is retarded and the timing of formation and the morphology of hydrates is affected. This short paper presents experimental results about the influence of delayed addition time of PCE SPs on hydration of cement and alite pastes, investigated by isothermal heat flow calorimetry. For cement as well as for alite pastes the hydration is retarded with SP, whereby the high charge PCE has a stronger retarding effect than the low charge PCE. The retardation caused by PCE is much more pronounced for alite than for cement mixes. If PCE is added later to the mix, the induction period is shortened and the hydration is accelerated compared to simultaneous addition. This applies for cement and alite pastes. With delayed PCE addition the alite shows a clearly less retarded setting and main hydration than after simultaneous addition. It is obvious that for alite pastes there is less retardation the later the addition of SP.
Während für die Bauwirtschaft in den meisten Ländern der nördlichen Halbkugel die Instandhaltung bestehender Strukturen und Infrastruktur im Vordergrund steht, geht es in vielen Ländern der Südhalbkugel in der Hauptsache um die Schaffung von Bauwerken und Infrastruktur zur Verwirklichung angemessener Lebensbedingungen, was wiederum das schnelle Wirtschaftswachstum weiter befeuert.
Beton ist als Massenbaustoff, trotz landläufig anderer Bewertung, aufgrund seines im Vergleich zu anderen Baustoffen günstigen CO2-Footprints und der globalen Verfügbarkeit hierbei aktuell ohne Alternative. Allerdings ist Beton nach Wasser das am zweithäufigsten genutzte Produkt auf Erden [1] und die globale Nachfrage und Produktion steigt dramatisch. Dies hat Konsequenzen für das globale Klima, denn gerade die als Bindemittel eingesetzten Portlandzemente verursachen bei ihrer Herstellung selbst unter modernsten Produktionsbedingungen große Mengen an CO2.
Deshalb müssen für zukünftige nachhaltigere Technologien neuartige Betone entwickelt werden, die bei gleicher oder verbesserter Leistungsfähigkeit, einen geringeren Bedarf an Portlandzement aufweisen.
Um den CO2-Ausstoß, der mit der Betonherstellung verbunden ist zu minimieren, müssen Anteile an Portlandzement im Bindemittel reduziert und durch nachhaltigere Ersatzstoffe ausgetauscht werden. Darüber hinaus muss das eingesetzte Bindemittel im Beton so effizient wie möglich ausgenutzt werden. Das heißt, ein Bauteil oder Bauwerk sollte gerade so viel Bindemittel enthalten, wie für die Tragfähigkeit und Dauerhaftigkeit erforderlich ist. Hierfür erscheint der Einsatz von leistungsfähigen bauchemischen Produkten unumgänglich. Diese können zum einen die veränderten Verarbeitungseigenschaften, die Zementersatzstoffe mit sich bringen, ausgleichen und gleichzeitig helfen, den Gesamtwassergehalt zu minimieren, so dass das Bindemittel seine maximale Leistungsfähigkeit erzielt. Fließmittel sind aktuell die wichtigsten Zusatzmittel für Beton. Sie reduzieren den Wasserbedarf und ermöglichen, Zement im Beton effizienter auszunutzen. Darüber hinaus sind Stabilisierer wichtig zur Erhöhung der Robustheit, insbesondere im Hinblick auf die bautechnischen Herausforderungen der Zukunft – vom Pumpen über weite Distanzen, dem Spritzen, dem Betonieren bei extremen Klimabedingungen bis hin zum 3D-Druck.