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In this paper, carbon fabric reinforced inorganic matrix composites were prepared. The inorganic matrix based on alkali activated aluminosilicate was used because of its resistance to fire and the temperatures up to 1000 °C. Influence of heat treatment of fabric, high temperature treatment of composite and preparation method on the mechanical properties and morphology of the composites were studied. The preparation of composites with the subsequent steps of impregnation, layering and curing of the composites was compared with the prepreg preparation method, which separates the impregnation of the reinforcement from the production of the composite. The SEM photographs show no differences in morphology between composites prepared from heat treated fabric and composites prepared from original fabrics. All four series of samples were comparatively saturated with matrix. Despite this, tensile properties of heat-treated fabric composites were negatively affected. While composites with heat-treated fabric reached the tensile strength up to 274 MPa, composites prepared without heat-treated fabric exhibited strengths higher than 336 MPa. Samples exposed to temperatures reaching 600 °C retained up to 40% of their original strength. The effect of composite preparation method on the tensile properties of the composites has not been proved.

This work presents carbon fabric reinforced aluminosilicate matrix composites with content of boric acid, where boron replaces aluminum ions in the matrix and can increase the mechanical properties of composites. Five different amounts of boric acid were added to the alkaline activator for preparing six types (including alkaline activator without boric acid) of composites by the prepreg method. The influence of boric acid content in the matrix on the tensile strength, Young’s modulus and interlaminar strength of composites was studied. Attention was also paid to the influence of boron content on the behavior of the matrix and on the internal structure of composites, which was monitored using a scanning electron microscope. The advantage of the aluminosilicate matrix is its resistance to high temperatures; therefore, tests were also performed on samples affected by temperatures of 400–800 °C. The interlaminar strength obtained by short-beam test were measured on samples exposed to 500 °C either hot (i.e. measured at 500 °C) or cooled down to room temperature. The results showed that the addition of boron to the aluminosilicate matrix of the prepared composites did not have any significant effect on their mechanical properties. The presence of boron affected the brittleness and swelling of the matrix and the differences in mechanical properties were evident in samples exposed to temperatures above 500 °C. All six prepared composites showed tensile strength higher than 320 MPa at laboratory temperature. The boron-free composite had the highest strength 385 MPa. All samples showed a tensile strength higher than 230 MPa at elevated temperatures up to 500 °C.

The present study focused on investigating the differences in properties between calcined and milled aluminosilicates with different particle size distributions. Two types of clay, i.e., kaolin and kaolinitic claystone, were subjected to calcination at 750 °C, and subsequent milling to obtain different fractions with distinct particle size distributions. These fractions were then combined with a potassium alkaline activator and quartz sand in a 50:50 weight ratio to form a geopolymer composite. The geopolymer binders were then characterized using a mercury intrusion porosimeter (MIP), scanning electron microscopy (SEM), and a rotary rheometer. Mechanical tests were conducted on the geopolymer composites prepared from aluminosilicates with varying particle size distributions. The findings indicated that aluminosilicates with a finer particle size distribution exhibited higher levels of dissolved aluminum (10,000 mg/kg) compared to samples with coarser particle size distributions (1000 mg/kg). Additionally, as the particle size distribution decreased, the dynamic viscosity of the geopolymer binders increased, while the average pore size decreased. Finally, the mechanical properties of the geopolymer composites derived from both tested aluminosilicates demonstrated a decline in performance as the mean particle size increased beyond 10 µm.

In this study, the effect of different types of aluminosilicates on the thermo-mechanical properties of metakaolinite-based geopolymer binders and composites was examined. The metakaolinite-based geopolymer binders and composites were produced from three different types of aluminosilicates (one metakaolin and two calcined claystones) and a potassium alkaline activator. Chamotte was added as a filler, amounting to 65% by volume, to create geopolymer composites. Geopolymer binders were characterized by X-ray diffraction, rotary rheometer and scanning electron microscopy. The mechanical properties, thermal dilatation and thermal conductivity were investigated on geopolymer composites with three different aluminosilicates before and after exposure to high temperatures (up to 1200 °C). The results showed that the geopolymer binders prepared from calcined claystones had a lower dynamic viscosity (787 and 588 mPa·s) compared to the geopolymer binders prepared from metakaolin (1090 mPa·s). Geopolymer composites based on metakaolin had lower shrinkage (0.6%) and higher refractoriness (1520 °C) than geopolymers from calcined claystones (0.9% and 1.5%, 1500 °C and 1470 °C). Geopolymers based on calcined kaolinitic claystones are a promising material with higher compressive (95.2 and 71.5 MPa) and flexural strength (12.4 and 10.7 MPa) compared to geopolymers based on metakaolin (compressive strength 57.7 MPa).

Six matrices based on alkali-activated aluminosilicate with different amounts of potassium phosphate were prepared for the production of six-layer composite plates. The addition of potassium phosphate in the matrix was 2 wt%, 4 wt%, 6 wt%, 8 wt% and 10 wt% of its total weight. The matrix without the potassium phosphate was also prepared. The aim of this study was to determine whether this addition has an effect on the tensile strength or Young’s modulus of composites at temperatures up to 800 °C. Changes in the thickness and weight of the samples after this temperature were also monitored. Carbon plain weave fabric was chosen for the preparation of the composites. The results show that under normal conditions, the addition of potassium phosphate has no significant effect on the mechanical properties; the highest measured tensile strengths were around 350 MPa. However, at temperatures of 600 °C and 800 °C the addition of potassium phosphate had a positive effect, with the tensile strength of the composites being up to 300% higher than the composites without the addition. The highest measured values of composites after one hour at 600 °C were higher than 100 MPa and after 1 h at 800 °C higher than 85 MPa.

A metakaolinite-based geopolymer binder was prepared by using calcined claystone as the main raw material and potassium as the alkaline activator. Chamotte was added (65 vol%) to form geopolymer composites. Potassium hydroxide (KOH) was used to adjust the molar ratio of K/Al and the effect of K/Al on thermo-mechanical properties of geopolymer composites was investigated. This study aimed to analyze the effect of K/Al ratio and exposure to high temperatures (up to 1200 °C) on the compressive and flexural strengths, phase composition, pore size distribution, and thermal dilatation. With an increasing K/Al ratio, the crystallization temperature of the new phases (leucite and kalsilite) decreased. Increasing content of K/Al led to a decline in the onset temperature of the major shrinkage. The average pore size slightly increased with increasing K/Al ratio at laboratory temperature. Mechanical properties of geopolymer composites showed degradation with the increase of the K/Al ratio. The exception was the local maximum at a K/Al ratio equal to one. The results showed that the compressive strength decreases with increasing temperature. For thermal applications above 600 °C, it is better to use samples with lower K/Al ratios (0.55 or 0.70).

Geopolymer foam is classified as a lightweight material with high porous in its matrix which has great offer for applications requiring fire-resistant, thermal, and acoustic properties. However, the high sensitivity to humid environments can be a major barrier of geopolymer foam that limits the variety of applications of this material. Based on this drawback, two types of hydrophobic agent (Lukosil M130 and Lukofob ELX) were used as an impregnator to treat the surface of geopolymer foam samples. This paper presented the results of water absorption properties of the untreated and treated geopolymer foam composites. The obtained properties were flexural strength, compressive strength, density, total water absorption, the rate of water absorption, and water absorption coefficient. The results showed that the samples after being impregnated with hydrophobic agents improved significantly their waterproof property especially using Lukosil M130. Moreover, the samples treated with Lukosil M130 had positive impact on their mechanical strength.

Background Lead, a serious threat for raptors, can hamper the success of their conservation. This study reports on experience with accidental lead intoxication and responses to chelation therapy in captive Cinereous ( Aegypius monachus ) and Egyptian ( Neophron percnopterus ) Vultures. Results Soil contamination by lead-based paint sanded off the steel aviary resulted in poisoning of eight Cinereous and two Egyptian Vultures. A male Egyptian Vulture developed signs of apathy, polydipsia, polyuria, regurgitation, and stupor, and died on the next day. Liver, kidney and blood lead concentrations were 12.2, 8.16 and 2.66 μg/g, respectively. Laboratory analyses confirmed severe liver and kidney damage and anaemia. Blood Pb levels of Pb-exposed Cinereous Vultures were 1.571 ± 0.510 μg/g shortly after intoxication, decreased to 0.530 ± 0.165 μg/g without any therapy in a month and to 0.254 ± 0.097 μg/g one month after CaNa 2 EDTA administration. Eight months later, blood lead levels decreased to close to the background of the control group. Blood parameters of healthy Pb-non-exposed Cinereous Vultures were compared with those of the exposed group prior to and after chelation therapy. Iron levels in the lead-exposed pre-treatment birds significantly decreased after chelation. Haematocrit levels in Pb-exposed birds were significantly lower than those of the controls and improved one month after chelation. Creatine kinase was higher in pre-treatment birds than in the controls but normalised after therapy. Alkaline phosphatase increased after chelation. A marked increase in the level of lipid peroxidation measured as thiobarbituric acid reactive species was demonstrated in birds both prior to and after chelation. The ferric reducing antioxidant power was significantly lower in pre-treatment vultures and returned to normal following chelation therapy. Blood metallothionein levels in lead-exposed birds were higher than in controls. Reduced glutathione dropped after CaNa 2 EDTA therapy, while oxidised glutathione was significantly lower in both pre- and post-treatment birds. A chick in an egg produced by a Cinereous Vulture female two months after lead toxicosis died on day 40 of artificial incubation. Lead concentrations in foetal tissues were consistent with levels causing avian mortality. Conclusions The reported blood parameters and reproduction impairment in captive birds may have implications for professionals dealing with lead exposure in wild birds.

The main causes of the damage of a compressor’s turbine blade are documented and described in the article. The turbine blade was made from titanium alloy grade 5 (VT6, Ti-6Al-4V). The analysed segments of the turbine blade were damaged by corrosion and erosion. The sample from the damaged blade was compared with an undamaged reference sample. The observed substantial distinctions between microstructure of the damaged and the reference sample were found using of light and scanning electron microscopy. The observed distinctions of the microstructure were caused by the differences in the heat treatment process.

This work describes the role of chemical composition and curing conditions in geopolymer strength, leachability of chemical elements and porosity. The study focuses on geopolymer material prepared from calcined kaolinite claystone, which is not studied frequently as a raw material for geopolymer production, although it has a high application potential as it is easily commercially available and allows preparation of geopolymers with low viscosity. The composition of geopolymers and their curing methods were selected considering their ease of use in the praxis. Therefore, the potassium water glass itself was used as alkali activator without any KOH or NaOH addition. Chemical composition was changed only by the density of water glass in the range of 1.2 to 1.6 g·cm−3. Geopolymers were cured at a temperature within the range of 5 °C–70 °C to speed up the solidification process as well as by microwave radiation. High compressive strengths were obtained for geopolymers with the highest densities of the water glass (1.5 and 1.6 g·cm−3) in dependence on various curing conditions. Higher strengths were achieved in the case of samples where the solidification was not accelerated. The samples cured at lower temperatures (5 °C) showed lower porosity compared to the other curing types. The lowest leachability of Si and alkalis was reached for the samples with water glass density 1.5 g·cm−3.