Alkali activation is studied as a potential technology to produce a group of high performance building materials from industrial residues such as metallurgical slag. Namely, slags containing aluminate and silicate form a useful solid material when activated by an alkaline solution. The alkali-activated (AA) slag-based materials are promising alternative products for civil engineering sector and industrial purposes. In the present study the locally available electric arc furnace steel slag (Slag A) and the ladle furnace basic slag (Slag R) from different metallurgical industries in Slovenia were selected for alkali activation because of promising amorphous Al/Si rich content. Different mixtures of selected precursors were prepared in the Slag A/Slag R ratios 1/0, 3/1, 1/1, 1/3 and 0/1 and further activated with potassium silicate using an activator to slag ratio of 1:2 in order to select the optimal composition with respect to their mechanical properties. Bending strength of investigated samples ranged between 4 and 18 MPa, whereas compressive strength varied between 30 and 60 MPa. The optimal mixture (Slag A/Slag R = 1/1) was further used to study strength development under the influence of different curing temperatures at room temperature (R. T.), and in a heat-chamber at 50, 70 and 90 °C, and the effects of curing time for 1, 3, 7 and 28 days was furthermore studied. The influence of curing time at room temperature on the mechanical strength at an early age was found to be nearly linear. Further, it was shown that specimens cured at 70 °C for 3 days attained almost identical (bending/compressive) strength to those cured at room temperature for 28 days. Additionally, microstructure evaluation of input materials and samples cured under different conditions was performed by means of XRD, FTIR, SEM and mercury intrusion porosimetry (MIP).
The presented research aimed at finding new ways to value hemp by-products (stalks) from the cannabidiol industry through thermochemical conversion. Chemical and elemental composition of hemp biomass was investigated by successive chemical extractions and Scanning Electron Microscopy along with Energy-dispersive X-ray Spectroscopy. Proximate and elemental analyses completed the chemical characterization of the hemp biomass and its biochar. Thermogravimetric analysis of the hemp biomass allowed to understand its kinetic of decomposition during thermal conversion. The carbon structure and porosity of the biochar were assessed by Raman spectroscopy and CO2 gas adsorption. Properties of interest were the energy production measured through calorific values, and the electrical conductivity. Two ways of valorisation of the hemp biomass were clearly identified, depending mainly on the chosen pyrolysis temperature. Hemp biochar carbonized at 400–600°C were classified as lignocellulosic materials with a good potential for solid biofuel applications. Specifically, the resulting carbonized biochar presented low moisture content (below 2.50%) favourable for high fuel quality, low volatile matter (27.1–10.4%) likely to show lower particle matter emissions, limited ash content (6.8–9.8%) resulting in low risk of fouling issues during the combustion, high carbon content (73.8–86.8%) suggesting strong energy density, associated with high higher heating values (28.45–30.95 MJ kg−1). Hemp biochar carbonized at 800–1000 °C displayed interesting electrical conductivity, opening opportunities for its use in electrical purposes. The electrical conductivity was related to the evolution of the biochar microstructure (development of graphite-like structure and changes in microporosity) in regard with the thermochemical conversion process parameters.
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