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Studies on Cement Pastes Exposed to Water and Solutions of Biological Waste
The paper presents studies on the early stages of biological corrosion of ordinary Portland cements (OPC) subjected to the reactive media from the agricultural industry. For ten months, cement pastes of CEM I type with various chemical compositions were exposed to pig slurry, and water was used as a reference. The phase composition and structure of hydrating cement pastes were characterized by X-ray diffraction (XRD), thermal analysis (DTA/TG/DTG/EGA), and infrared spectroscopy (FT-IR). The mechanical strength of the cement pastes was examined. A 10 to 16% decrease in the mechanical strength of the samples subjected to pig slurry was observed. The results indicated the presence of thaumasite (C3S·CO2·SO3·15H2O) as a biological corrosion product, likely formed by the reaction of cement components with living matter resulting from the presence of bacteria in pig slurry. Apart from thaumasite, portlandite (Ca(OH)2)—the product of hydration—as well as ettringite (C3A·3CaSO4·32H2O) were also observed. The study showed the increase in the calcium carbonate (CaCO3) phase. The occurrence of unreacted phases of cement clinker, i.e., dicalcium silicate (C2S) and tricalcium aluminate (C3A), in the samples was confirmed. The presence of thaumasite phase and the exposure condition-dependent disappearance of CSH phase (calcium silicate hydrate), resulting from the hydration of the cements, were demonstrated.
Correction: Durczak et al. Modern Methods of Asbestos Waste Management as Innovative Solutions for Recycling and Sustainable Cement Production. Sustainability 2024, 16, 8798
The authors would like to make the following corrections to the published paper [...]
Physicochemical properties of Mn1.45Co1.45Cu0.1O4 spinel coating deposited on the Crofer 22 H ferritic steel and exposed to high-temperature oxidation under thermal cycling conditions
AbstractThe Crofer 22 H ferritic steel substrate was coated with an Mn1.45Co1.45Cu0.1O4 spinel by means of electrophoresis. After high-temperature oxidation under thermal cycling conditions, the physicochemical properties of the obtained system were evaluated. During 48-h cycles that involved heating the samples up to temperatures of either 750 or 800 °C, the oxidation kinetics of both coated and unmodified steel approximately obeyed the parabolic rate law. The unmodified steel was oxidized at a higher rate than the system consisting of the substrate and the coating. In its bulk form, the spinel consisted entirely of the cubic phase and it exhibited high electrical conductivity. The Mn1.45Co1.45Cu0.1O4 coating, on the other hand, was compact and consisted of two phases—the cubic and the tetragonal one—and it was characterized by good adhesion to the metallic substrate. After cyclic oxidation studies conducted for the two investigated temperatures (750 or 800 °C), the coating was determined to provide a considerable improvement in the electrical properties of the Crofer 22 H ferritic steel, as demonstrated by the area-specific resistance values measured for the steel/coating system. The evaporation rate of chromium measured for these samples likewise indicates that the coating is capable of acting as an effective barrier against the formation of volatile compounds of chromium. The Mn1.45Co1.45Cu0.1O4 spinel can therefore be considered a suitable material for a coating on the Crofer 22 H ferritic steel, with intermediate-temperature solid oxide electrolyzer cells as the target application.
Efficient Management of Asbestos Waste Through Utilization as Mineral Additives in Portland Cement Production
This article presents research on the effectiveness of utilizing asbestos waste, particularly chrysotile asbestos, in the production of Portland cement. The study aimed to evaluate the feasibility of transforming asbestos cement (Eternit) through thermal treatment and its enrichment with mineral additives, enabling its integration into the clinker synthesis process. Differences in the physicochemical properties of types of cement produced from conventional raw materials and those manufactured using asbestos waste were analyzed. The research findings indicate that the presence of asbestos in cementitious materials leads to a significant mass loss of 29.4% due to thermal decomposition. Chemical analysis revealed the presence of aluminum oxide (Al2O3) and iron oxide (Fe2O3) at levels of 4.10% and 3.54%, respectively, suggesting the formation of brownmillerite, a phase typical of cement clinker. Furthermore, compressive strength tests on asbestos-modified cements demonstrated comparable mechanical properties to reference cement (CEM I), indicating their potential applicability in construction. This study provides essential insights into the mineralogical composition of asbestos cement, which is crucial for developing effective methods for its safe disposal. It represents a significant step toward sustainable asbestos waste management and the promotion of innovative solutions in the construction industry.
Cement Carbonation Under Fermentation Conditions as a Tool for CO2 Emission Management—Technological, Environmental and Economic Analysis
The aim of this study is an interdisciplinary assessment of the potential of cement pastes to permanently bind carbon dioxide (CO2) under anaerobic digestion conditions, considering technological, microstructural, environmental, and economic aspects. The research focused on three types of Portland cement: CEM I 52.5N, CEM I 42.5R-1, and CEM I 42.5R-2, differing in phase composition and reactivity, which were evaluated in terms of their carbonation potential and resistance to chemically aggressive environments. The cement pastes were prepared with a water-to-cement ratio of 0.5 and subjected to 90-day exposure in two environments: a reference environment (tap water) and a fermentation environment (aqueous suspension of poultry manure simulating biogas reactor conditions). XRD, TG/DTA, SEM/EDS, and mercury intrusion porosimetry were applied to analyze CO2 mineralization, phase changes, and microstructural evolution. XRD results revealed a significant increase in calcite content (e.g., for CEM I 52.5N from 5.9% to 41.1%) and the presence of vaterite (19.3%), indicating intense carbonation under organic conditions. TG/DTA analysis confirmed a reduction in portlandite and C-S-H phases, suggesting their transformation into stable carbonate forms. SEM observations and EDS analysis revealed well-developed calcite crystals and the dominance of Ca, C, and O, confirming effective CO2 binding. In control samples, hydration products predominated without signs of mineralization. The highest sequestration potential was observed for CEM I 52.5N, while cements with higher C3A content (e.g., CEM I 42.5R-2) exhibited lower chemical resistance. The results confirm that carbonation under fermentation conditions may serve as an effective tool for CO2 emission management, contributing to improved durability of construction materials and generating measurable economic benefits in the context of climate policy and the EU ETS. The article highlights the need to integrate CO2 sequestration technologies with emission management systems and life cycle assessment (LCA) of biogas infrastructure, supporting the transition toward a low-carbon economy.
Governance Matters: Evidence from Global Analysis on Environmental Sustainable Development Goals
This study explores how governance acts as a critical mediator between key environmental Sustainable Development Goals (SDGs)—SDG 13 (Climate Action), SDG 14 (Life Below Water), and SDG 15 (Life on Land)—and overall sustainability performance. Leveraging global datasets from the UN SDG framework and World Bank Governance Indicators, we construct a composite governance index using Principal Component Analysis (PCA) to capture institutional quality. Through mediation and path analysis, we reveal striking patterns: governance amplifies the positive impact of SDG 15 on the overall SDG Index, underscoring its role in biodiversity and land management. Conversely, governance introduces an adverse indirect effect for SDG 13, highlighting institutional and regulatory gaps that weaken climate policy outcomes. No significant mediation is observed for SDG 14, indicating strong contextual dependencies in marine governance. These findings confirm governance as a pivotal driver—either reinforcing or constraining environmental progress. Strengthening governance frameworks through transparency, accountability, and regulatory quality can accelerate progress toward the SDGs and advance the 2030 Agenda. This study provides empirical evidence on governance as a mediator and deepens understanding of institutional mechanisms shaping sustainability trajectories.
Effect of Variable Synthesis Conditions on the Formation of Ye’elimite-Aluminate-Calcium (YAC) Cement and Its Hydration in the Presence of Portland Cement (OPC) and Several Accessory Additives
In the presented study, ye’elimite-aluminate-calcium (YAC) cement was synthesized. Complete synthesis of crystalline phases was achieved at a temperature of 1300 °C, which is 150 °C lower than the temperature standardly used in the processes of obtaining calcium aluminate cements (CAC). The greatest amount of ye’elimite phase (Klein complex), roughly 87% by mass, was acquired utilizing a sulphur ion transporter derived from artificial dihydrate gypsum obtained in the flue gas desulphurization process (variation I). In the case of anhydrite, the amount of synthesized crystalline ye’elimite in the clinker was 67% by weight (variant II). Depending on the synthesis conditions in the clinkers, the quantity of obtained calcium aluminates (C12A7, CA, and CA2) ranged from 20 to 40% by weight. Studies on the hydration process of YAC cement samples showed that the main products are hydrated calcium aluminates and dodecahydrate calcium alumino-sulphate. In sinters of YAC and OPC, no crystalline ettringite was observed. Hydration analysis of Chinese cement revealed the presence of crystalline ettringite and dodecahydrate calcium alumino-sulphate, as well as hydrated calcium silicates of the CSH type accompanied with pseudo-crystalline Al(OH)3. The obtained clinkers from variants I and II constitute a special binder, which, due to its phase composition after hydration, can be used in the construction of reactors for biogas production in eco-energy applications.
Modern Methods of Asbestos Waste Management as Innovative Solutions for Recycling and Sustainable Cement Production
Managing asbestos waste presents a significant challenge due to the widespread industrial use of this material, and the serious health and environmental risks it poses. Despite its unique properties, such as resistance to high temperatures and substantial mechanical strength, asbestos is a material with well-documented toxicity and carcinogenicity. Ensuring the safe removal and disposal of asbestos-containing materials (ACM) is crucial for protecting public health, the environment, and for reducing CO2 emissions resulting from inefficient waste disposal methods. Traditional landfill disposal methods have proven inadequate, while modern approaches—including thermal, chemical, biotechnological, and mechanochemical methods—offer potential benefits but also come with limitations. In particular, thermal techniques that allow for asbestos degradation can significantly reduce environmental impact, while also providing the opportunity to repurpose disposal products into materials useful for cement production. Cement, a key component of concrete, can serve as a sustainable alternative, minimizing CO2 emissions and reducing the need for primary raw materials. This work provides insights into research on asbestos waste management, offering a deeper understanding of key initiatives related to asbestos removal. It presents a comprehensive review of best practices, innovative technologies, and safe asbestos management strategies, with particular emphasis on their impact on sustainable development and CO2 emission reduction. Additionally, it discusses public health hazards related to exposure to asbestos fibers, and worker protection during the asbestos disposal process. As highlighted in the review, one promising method is the currently available thermal degradation of asbestos. This method offers real opportunities for repurposing asbestos disposal products for cement production; thereby reducing CO2 emissions, minimizing waste, and supporting sustainable construction.
The Effect of Biological Corrosion on the Hydration Processes of Synthetic Tricalcium Aluminate (C3A)
This paper presents a study related to the biological degradation of a tricalcium aluminate (C3A) phase treated with reactive media from the agricultural industry. During one month of setting and hardening, synthetic C3A was subjected to corrosion in corn silage, pig slurry and chicken manure. The hardening process of the C3A phase in water was used as a reference sample. The phase composition and microstructure of the hydrating tricalcium aluminate slurries were characterised by X-ray diffraction (XRD), thermal analysis (DTA/TG/DTG/EGA), scanning microscopy (SEM, EDS) and infrared spectroscopy (FT-IR). In the samples studied, it was observed that the qualitative and quantitative phase composition of the synthetic tricalcium aluminate preparations changed depending on the corrosion exposure conditions. The main crystalline phases formed by the hydration of the examined samples in water as well as in corrosive media were the catoite (Ca3Al2(OH)12) and hydrocalumite (Ca2Al(OH)7·3H2O) phases. Detailed analysis showed the occurrence of secondary crystallisation in hydrating samples and the phases were mainly calcium carbonates (CaCO3) with different crystallite sizes. In the phase composition of the C3A pastes, varying amounts of aluminium hydroxides (Al(OH)3) were also present. The crystalline phases formed as a result of secondary crystallisation represented biological corrosion products, probably resulting from the reaction of hydrates with secondary products resulting from the metabolic processes of anaerobic bacterial respiration (from living matter) associated with the presence of bacteria in the reaction medium. The results obtained contribute towards the development of fast-acting and bio-corrosion-resistant special cements for use in bioenergetics.
Synthesis and Investigation of the Hydration Degree of CA2 Phase Modified with Boron and Fluorine Compounds
This study investigated the effect of fluoride and boron compound additives on the synthesis and hydration process of calcium aluminate (CA2). The analysis showed that the temperature of the full synthesis of CA2 without mineralizing additives was 1500 °C. However, the addition of fluorine and boron compounds at 1% and 3% significantly reduced the synthesis temperature to a range of 1100–1300 °C. The addition of fluoride compounds did not result in the formation of fluoride compounds from CaO and Al2O3, except for the calcium borate phase (Ca3(BO3)2) under certain conditions. In addition, the cellular parameters of the synthesized calcium aluminate phases were not affected by the use of these additives. Hydration studies showed that fluoride additives accelerate the hydration process, potentially improving mechanical properties, while boron additives slow down the reaction with water. These results highlight the relevance of fluoride and boron additives to the synthesis process and hydration kinetics of calcium aluminate, suggesting the need for further research to optimize their application in practice. TG studies confirmed the presence of convergence with respect to X-ray determinations made. SEM, EDS and elemental concentration maps confirmed the presence of a higher Al/Ca ratio in the samples and also showed the presence of hexagonal and regular hydration products.
Management of Chemical Synthesis Processes of Potassium Humate During Coal Beneficiation Waste Processing
The growing accumulation of coal beneficiation waste represents a significant environmental and technological challenge while simultaneously creating opportunities for the resource recovery within circular economy frameworks. This study presents the development and process-oriented evaluation of an environmentally safe technology for converting coal beneficiation waste into potassium humate, with the simultaneous recovery of molybdenum compounds via alkaline extraction. The proposed solution is designed to improve resource efficiency, reduce the volume of waste directed to landfilling, and generate a high value-added product for agricultural and technological applications. The process flow includes preliminary characterization and preparation of the waste, determination of moisture, ash, and organic matter content, and the separation of metal-bearing fractions. Alkaline extraction was carried out using potassium hydroxide under controlled temperature and reaction time conditions, followed by purification and concentration of the humate solution. The process management strategy focuses on optimizing key technological parameters, including alkali concentration, solid-to-liquid ratio, temperature, and reaction time, to maximize humate yield while preserving functional groups responsible for biological activity. Comprehensive physicochemical, thermal, and mineralogical analyses confirmed the stability of the aluminosilicate matrix and the suitability of the material for alkaline processing without adverse structural degradation. Biological tests using oat (Avena sativa) demonstrated that potassium humate derived from coal beneficiation waste exhibits higher growth-stimulating effectiveness than a conventional commercial humate. Economic analysis revealed a strong correlation between humic acid content and added value, confirming the feasibility of transforming coal beneficiation waste from an environmental burden into a valuable secondary resource.
The Energy Footprint in the EU: How CO2 Emission Reductions Drive Sustainable Development
Understanding how sectoral CO2 emissions shape sustainable development outcomes is essential for designing effective energy and economic strategies within the European Union (EU). This study presents a multidimensional analysis of CO2 emissions, the contributions of individual sectors, and their connections to the Sustainable Development Goals (SDGs). Using Bayesian network analysis, the research identifies significant interdependencies between emission reductions and progress in sustainable development, highlighting the complex relationship between energy transition, economic growth, and social justice. The findings show that total CO2 emissions in the EU have decreased since 1990; however, the rate of reduction varies across sectors and member states. The most substantial decreases have been recorded in the energy sector, while industrial processes and agriculture show slower progress. Economic crises, such as the 2008 financial collapse and the COVID-19 pandemic, have led to temporary declines in emissions; however, lasting achievements in sustainability require structural transformations rather than short-term disruptions. The Bayesian model reveals strong connections between emission reductions and progress on clean energy (SDG 7), responsible consumption (SDG 12), and climate action (SDG 13), while also indicating indirect impacts on economic growth (SDG 8) and social equity. This highlights the importance of integrated policymaking to maximise the benefits of sustainable development. This study provides a data-driven foundation for enhancing EU climate strategies, ensuring that emission reductions support environmental goals, economic resilience, and social well-being.
Changes in the Phase Composition of Calcium Aluminoferrites Based on the Synthesis Condition and Al2O3/Fe2O3 Molar Ratio
The presented work concerns the study of the changes in the phase composition of calcium aluminoferrites which depend on the synthesis conditions and the selection of the Al2O3/Fe2O3 molar ratio (A/F). The A/F molar ratio extends beyond the limiting composition of C6A2F (6CaO·2Al2O3·Fe2O) towards phases richer in Al2O3. An increase in the A/F ratio above unity favours the formation of other crystalline phases such as C12A7 and C3A, in addition to calcium aluminoferrite. Slow cooling of melts characterised by an A/F ratio below 0.58, results in the formation of a single calcium aluminoferrite phase. Above this ratio, the presence of varying contents of C12A7 and C3A phases was found. The process of rapid cooling of the melts with an A/F molar ratio approaching the value of four favours the formation of a single phase with variable chemical composition. Generally, an increase in the A/F ratio above the value of four generates the formation of a calcium aluminoferrite amorphous phase. The rapidly cooled samples with compositions of C22.19A10.94F and C14.61A6.29F were fully amorphous. Additionally, this study shows that as the A/F molar ratio of the melts decreases, the elemental cell volume of the calcium aluminoferrites decreases.