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Dr. Cristina Ruiz Agudo

Gruppenleitung

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Phone: +49 7531  88-2169

Room: L1004

Post office box: 714

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Responsibilities

Physikalische Chemie

– Nicht-klassische Kristallisation industriell relevanter Materialien
– Analyse und Methodenentwicklung zur Untersuchung von Kristallisationsprozessen
– Biomineralisation
– Additiv-gesteuerte Kristallisation

Michaela Köst

Sekretärin

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Phone: +49 7531  88-2027

Room: L 1002

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Maximilian Marsiske

Ph.D. Student

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Phone: +49 7531  88-4453

Room: L1049

Post office box: 714

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Responsibilities

– Nicht-klassische Kristallisation industriell relevanter Materialien
– Analyse und Methodenentwicklung zur Untersuchung von Kristallisationsprozessen
– Additiv-gesteuerte Kristallisation

Marc Staiger

Ph.D. Student

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Phone: +49 7531  88-4808

Room: L1051

Post office box: 714

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Responsibilities

My research concentrates on the understanding of homogeneous crystallisation processes of calcium silicate hydrates (C-S-H), which is the most important compound in modern cement. The main focus lies here in the pre-nucleation and early post-nucleation regime. Further, the influence of zinc on the nucleation of C-S-H is investigated, since it’s one of the most common impurities in cement. Another topic is the influence of dehydration processes (e. g. due to cosmotropic/chaotropic effects) on pre-nucleation species of C-S-H and the altering on its nucleation pathway. In general, all C-S-H is synthesised with simple silicon and calcium precursors via automated titration set-ups.

The crystallisation process is in-situ monitored with different electrodes and the obtained solid & pre-nucleation species are respectively analysed with the following methods: FT-IR, PXRD, TGA, SEM/EDX & (HR)TEM/EDX/ED, AUC, ToF-MS.

Yannick Emminger

Ph.D. Student

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Phone: +49 7531  88-4808

Room: L1051

Post office box: 714

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Responsibilities

Physical Chemistry

Towards sustainable cements: Understanding the crystallization of cementitious hydrates in LC3 blends as eco-friendly binder

Limestone calcined clay cements (LC3) are a very special and promising type of new cements. They take advantage of synergistic effects in the interaction of calcined clay and limestone as supplementary cementitious materials. With these cements it is already possible to reduce the clinker content to less than 50% and thus save more than 30% in CO2 emissions. Additionally, LC3 blends are roughly 15-25% cheaper in production than ordinary Portland Cement (OPC). However, one of the few disadvantages still lies in the rheology of calcined clay-containing materials. Once water has been added, they are not as easy to handle as traditional Portland cement, making them somewhat more difficult to work with on the construction site. 

This is where the research of Yannick Emminger comes in and tries to find a way to firstly investigate and secondly influence the crystallisation of the different hydrates in LC3, making it more applicable for construction. Hereby, the hydrates (C-S-H, C-A-S-H, ettringite, calcium carboaluminates, AFm and AFt phases,...) are synthesised via a precipitation reaction from an aqueous solute phase and subsequently analysed. The aim is to monitor the nucleation and control it through additive assistance. For that, analytical methods like FTIR, SEM, EDX, TEM, SAED, TGA, ITC, XRD, DLS, AUC, 1H-/ 13C-/ 27Al-/ 29Si-NMR, and more, are used.

Annika Bastian

Ph.D. Student

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Phone: +49 7531  88-4808

Room: L1051

Post office box: 714

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Responsibilities

Research: The effect of additives on Mg-based cement hydrates

Mg-based cements are a promising cement alternative and have the potential to become CO2-neutral depending on the raw materials and technology used. However, their properties are not yet comparable with ordinary CaO-based cement (Portland cement). They suffer from a high demand for water, and a rapid loss of workability. To ensure the workability of the blends the use of superplasticizers in Mg-based binders is essential.
Phosphorous- and carboxylic-based additives have the potential to reduce the water demand of magnesium silicate cement. Therefore, by synthesizing different Mg-cement hydrates in an automated titration setup, I study the effect of these additives on the main Mg phases (i.e., magnesium silicate hydrate (M-S-H), magnesium hydroxide, magnesium carbonate). By monitoring the pH, conductivity, and transmittance, in combination with ex-situ analysis (FTIR, SEM, TEM, EDX, PXRD, TGA) of the final products, the effect of P- and carboxylic-based additives on Mg-cement hydrates is investigated to identify suitable superplasticizer(s) and the optimal dosages for Mg-based cement to make them applicable for industrial purposes. 

Patricia Besirske

Ph.D. Student

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Phone: +49 7531  88-5462

Room: L 1052

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Marco Genovesi

Ph.D. Student

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Phone: +49 7531  88-5462

Room: L 1052

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Britta Maier

Ph.D. Student

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Phone: +49 7531  88-5462

Room: L 1052

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Responsibilities

Project title:

Towards Monodispersity in Biomimetic Silica-Carbonate Microstructures

Project description:

In my research, I focus on optimizing the synthesis of biomimetic silica-carbonate microstructures (so-called Silica-Biomorphs) towards a selective, monodisperse production of the individual morphologies.

Silica-Biomorphs are a completely inorganic alternative to form microstructures showing a variety of biomimetic morphologies from atmospheric carbon dioxide and an alkaline solution containing silicate and alkaline earth metal salts. Thus, differently sized and shaped structures that can reach lengths of several hundred micrometres to millimetres can be obtained. They consist of amorphous silicon dioxide and self-assembled alkaline earth metal carbonate nanocrystals.

So far, the exact mechanisms of the formation and the factors influencing the self-assembly of the nanocrystallites and thereby the resulting morphology are still largely unknown. This knowledge, though, is necessary for the selective production of defined structures that allow the investigation of shape-property relationships to lead to new applications.

Therefore, I developed a flow cell setup that allows knowledge and control over system parameters during the reaction. With this, experiments are carried out to screen those system parameters and gain new insights into the dependence of the synthetic parameters on the morphological outcome. This already enabled a new selective synthesis of coral-like structures and could also make deterministic syntheses of other desired morphologies accessible in the future.

Lisa Huber

Master Studentin

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Phone: +49 7531  88-4808

Room: L1051

Post office box: 714

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Angelina Graf

Master Studentin

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