Analytische Chemie
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Rice husk as (RHA) is an eco-friendly material, which can be used as a supplementary cementitious material (SCM) in cement and concrete. Due to the high water demand for the material, superplasticizers (SPs) are essential to improve the performance. However, the interaction between the SPs and RHA systems is limited. This paper investigates the interaction of the binders with three SPs, i.e. two polycarboxylate ethers (PCEs) and one lignosulphonate (LS). The investigations are performed on blended systems of mortar containing various percentages of RHA and limestone powder (LSP). LSP is used in this research to improve the workability of the mortar. The results from the zeta potential (ZP) shows that the SPs are extremely dependent on the pH of the suspension. At higher pH values such as in a cementitious system, the ZP becomes less negative indicating that the ions in the suspension interact with the carboxyl groups in the backbone of the polymers thus reducing the surface charges of the SP. The mini-slump flow shows that the workability of the blended mortar systems is significantly improved with the addition of SPs. LS systems with increasing RHA is observed to have similar workability as the control mix over time. The compressive strength test results show increased strength for all mortar specimens with added RHA and LSP at later ages.
Designing the shape and size of catalyst particles, and their interfacial charge, at the nanometer scale can radically change their performance. We demonstrate this with ceria nanoparticles. In aqueous media, nanoceria is a functional mimic of haloperoxidases, a group of enzymes that oxidize organic substrates, or of peroxidases that can degrade reactive oxygen species (ROS) such as H2O2 by oxidizing an organic substrate. We show that the chemical activity of CeO2−x nanoparticles in haloperoxidase- and peroxidaselike reactions scales with their active surface area, their surface charge, given by the ζ-potential, and their surface defects (via the Ce3+/Ce4+ ratio). Haloperoxidase-like reactions are controlled through the ζ-potential as they involve the adsorption of charged halide anions to the CeO2 surface, whereas peroxidase-like reactions without charged substrates are controlled through the specific surface area SBET. Mesoporous CeO2−x particles, with large surface areas, were prepared via template-free hydrothermal reactions and characterized by small-angle X-ray scattering. Surface area, ζ-potential and the Ce3+/Ce4+ ratio are controlled in a simple and predictable manner by the synthesis time of the hydrothermal reaction as demonstrated by X-ray photoelectron spectroscopy, sorption and ζ-potential measurements. The surface area increased with synthesis time, whilst the Ce3+/Ce4+ ratio scales inversely with decreasing ζ-potential. In this way the catalytic activity of mesoporous CeO2−x particles could be tailored selectively for haloperoxidase- and peroxidase-like reactions. The ease of tuning the surface properties of mesoporous CeO2x particles by varying the synthesis time makes the synthesis a powerful general tool for the preparation of nanocatalysts according to individual needs.