This article presents the influence of three additions i.e., hydroxyethyl methyl cellulose (HEMC), sodium bicarbonate and flue gas desulfurization (FGD) gypsum on the porosity of gypsum-based materials. The specific microstructure for a material with good thermal insulation properties i.e., numerous closed pores distributed in the binding matrix, was achieved using HEMC (0.3 wt.%) and sodium bicarbonate (0.5–2 wt.%). The addition of HEMC to the gypsum binder determines, as expected, an increase of the porosity due to its ability to stabilize entrained air. In the case of a sodium bicarbonate addition, the pores are formed in the binding matrix due to the entrapment of the gas (CO₂) generated by its reaction. Sodium bicarbonate addition delays the setting of gypsum binder therefore in this study FGD gypsum (waste produced in the desulfurization process of combustion gases generated in power plants) was also added to the mixture to mitigate this negative effect. The decrease of geometrical density (up to 13%, in correlation with the additive nature and dosage) correlated with the increase of the porosity, determines, as expected, the decrease of flexural and compressive strengths (33–75%), but improves the thermal properties i.e., decreases the thermal conductivity (9–18%).

This paper presents the main properties of magnesium phosphate cements (MPCs) to be used as coatings for passive fire protection of steel structures. The influence of various additions, i.e., waste glass powder, fly ash, a styrene–acrylic dispersion, and expandable graphite, on the fire behavior and the adhesion to steel substrates of magnesium phosphate coatings is presented in this paper. The setting time of studied cements is extended when magnesia, the main component of MPCs, is partially replaced with fly ash or/and waste glass powder. The mineralogical composition of these cements, before and after thermal treatment at 1050 °C, was assessed by X-ray diffraction and could explain the changes in compressive strength, volume, and mass recorded for the thermally treated specimens. The studied magnesium phosphate coatings have a good adherence to the steel substrate (assessed by a pull-off test) both before and after direct contact with a flame (fire test) and decrease the temperature of the steel substrate by 30% with respect to the one recorded for the uncoated steel plate.

The paper presents the obtention and characterization of Portland cement mortars with limestone filler and nano-calcite additions. The nano-calcite was obtained by the injection of CO₂ in a nano-Ca(OH)₂ suspension. The resulted nano-CaCO₃ presents different morphologies, i.e., polyhedral and needle like crystals, depending on the initial Ca(OH)₂ concentration of the suspension. The formation of calcium carbonate in suspensions was confirmed by X-ray diffraction (XRD), complex thermal analysis (DTA-TG), scanning electron microscopy (SEM) and transmission electron microscopy (TEM and HRTEM). This demonstrates the viability of this method to successfully sequestrate CO₂ in cement-based materials. The use of this type of nano-CaCO₃ in mortar formulations based on PC does not adversely modify the initial and final setting time of cements; for all studied pastes, the setting time decreases with increase of calcium carbonate content (irrespective of the particle size). Specific hydrated phases formed by Portland cement hydration were observed in all mortars, with limestone filler additions or nano-CaCO₃, irrespective of curing time. The hardened mortars with calcium carbonate additions (in adequate amounts) can reach the same mechanical strengths as reference (Portland cement mortar). The addition of nano-CaCO₃ in the raw mix increases the mechanical strengths, especially at shorter hardening periods (3 days).

The aim of this study is to assess the possibility of obtaining phosphate cements based on dolomite calcined at various temperatures with/without quartz sand addition. A lower calcination temperature of dolomite (1200 °C) determines a high increase in the system temperature when calcined dolomite is mixed with KH₂PO₄ (MKP) solution and also a rapid expansion of the paste. The increase in calcination temperature up to 1400 °C reduces the oxides reactivity; however, for lower dosages of MKP, the expansion phenomenon is still recorded. The increase in MKP dosage increases the compressive strength due to the formation of K-struvite. The mixing of dolomite with sand, followed by thermal treatment at 1200 °C, modifies its composition and reactivity; the compressive strength of phosphate cements obtained by mixing this solid precursor with MKP increases up to 28 days of curing. We assessed the nature of hydrates formed in the phosphate systems studied by X-ray diffraction in order to explain the hardening processes and the mechanical properties of these systems. The microstructure and elemental composition of hardened cement pastes were assessed by scanning electronic microscopy with energy-dispersive spectroscopy. The phosphate cements based on calcined magnesite or dolomite were used to immobilize an industrial hazardous waste with high chromium content. The partial substitution of calcined magnesite/dolomite with this waste determines an important decrease in compressive strengths. Nevertheless, the leaching tests confirm an adequate immobilization of chromium in some of the matrices studied (for a waste dosage corresponding to 0.5 wt % Cr).

Porous alkali activated materials (AAM), can be obtained from waste glass powder and slag mixtures by alkali activation with NaOH solution. To obtain an adequate porous microstructure, the hardened AAM pastes were thermally treated at temperatures ranging between 900°C and 1000°C, for 60 or 30 minutes. Due to the intumescent behaviour specific for this type of materials, an important increase of the volume and porosity occurs during the thermal treatment. The partial substitution of waste glass powder with slag, determines the increase of compressive strength assessed before (up to 37 MPa) and after (around 10 MPa) thermal treatment; the increase of slag dosage also determines the increase of the activation temperature of the intumescent process (above 950°C). The high porosity and the specific microstructure (closed pores with various shapes and sizes) of these materials recommend them to be utilised as thermal and acoustical insulation materials.

Fireproof inorganic coatings based on sodium silicate solution with intumescent additions were prepared and tested to assess their ability to limit the negative effect of a fire. The intumescent materials were obtained by the alkali activation of waste glass powder (obtained by the grinding of recycled soda-lime culet) and slag (waste resulting from the metallurgical industry). The replacement of talc (used as filler in paint formulation) with the intumescent materials obtained by the alkaline activation of waste glass powder (WGP), determined an increase in the intumescence coefficient (up to 65%) and decreased the activation temperature of this process. To evaluate these coatings’ abilities to prevent or delay the temperature increase in metal structures, the paints were applied on steel plates and tested in direct contact with the flame of a butane burner for 60 min. The coatings prevented the increase in the steel substrate temperature over one considered critical (500°C) for steel mechanical properties; the combination of two coatings, with different intumescence activation temperatures, correlated with the increase in the coating’s thickness, sensibly reduced the rate of temperature increase (up to 75%) in the steel substrate.