Search Results (33)

The priming effect (PE), a microbially mediated process, critically regulates the balance between carbon sequestration and mineralization. This study used soils from different soil depths (0–20 cm, 20–40 cm, and 40–60 cm) under Picea schrenkiana forest in the Tianshan Mountains as the research object. An indoor incubation experiment was conducted by adding three concentrations (1% SOC, 2% SOC, and 3% SOC) of ¹³C-labelled glucose. We applied ¹³C isotope probe-phospholipid fatty acid (PLFA-SIP) technology to investigate the influence of readily labile organic carbon inputs on soil priming effect (PE), microbial community shifts at various depths, and the mechanisms underlying soil PE. The results indicated that the addition of ¹³C-labeled glucose accelerated the mineralization of soil organic carbon (SOC); CO₂ emissions were highest in the 0–20 cm soil layer and decreased trend with increasing soil depth, with significant differences observed across different soil layers (p < 0.05). Soil depth had a positive direct effect on the cumulative priming effect (CPE); however, it showed negative indirect effects through physico-chemical properties and microbial biomass. The CPE of the 0–20 cm soil layer was significantly positively correlated with ¹³C-Gram-positive bacteria, ¹³C-Gram-negative bacteria, and ¹³C-actinomycetes. The CPE of the 20–40 cm and 40–60 cm soil layers exhibited a significant positive correlation with cumulative mineralization (CM) and microbial biomass carbon (MBC). Glucose addition had the largest and most significant positive effect on the CPE. Glucose addition positively affected PLFAs and particularly microbial biomass. This study provides valuable insights into the dynamics of soil carbon pools at varying depths following glucose application, advancing the understanding of forest soil carbon sequestration. Full article

Concrete production contributes nearly 8% of the global CO₂ emissions, making carbon capture in construction materials a critical environmental priority. While microbial self-healing concrete has shown promise in repairing structural cracks, its potential to serve as a carbon-negative material through atmospheric CO₂ sequestration remains underutilized. This interdisciplinary review—designed for materials scientists, civil engineers, and environmental technologists—systematically evaluates bacterial candidates for their application in self-healing, carbon-capturing concrete. Bacteria are ranked according to their efficiency in capturing CO₂ through both direct mechanisms (e.g., photosynthetic fixation by cyanobacteria) and indirect pathways (e.g., ureolysis-driven calcium carbonate precipitation). The assessment also considers microbial survivability in high-alkalinity concrete environments, the effectiveness of encapsulation strategies in enhancing bacterial viability and function over time, and sustainability metrics such as those derived from life cycle assessment (LCA) analyses. The findings highlight Bacillus sphaericus and Sporosarcina pasteurii as high-performing species in terms of rapid mineralization and durability, while encapsulation significantly improves the long-term viability for species like Paenibacillus mucilaginosus and Synechococcus. Notably, Bacillus sphaericus and Sporosarcina pasteurii exhibit carbonate precipitation rates of 75–100 mg CaCO₃/g biomass and enable crack closure of up to 0.97 mm within 8 weeks. The proposed bacterial ranking framework, paired with performance data and environmental modeling, provides a foundation for the advancement of scalable, carbon-negative concrete solutions. Full article

The efficiency of electrochemical advanced oxidation processes (EAOPs) is fundamentally governed by hydroxyl-radical (•OH) generation. While direct experimental measurements of these transient species remain complex and impractical, robust computational methods for predicting their temporal profiles are notably scarce. This work presents a semi-empirical methodology based on H₂O₂ measuring experiments that enables indirect •OH quantification. We employed a recently developed carbon-based electrode and the priority pollutant bisphenol A (BPA) as the model system. The system achieved 92.3% BPA degradation with 84% mineralization efficiency during 5-h electrooxidation at 15 mA/cm². Gas chromatography/mass spectrometry (GC/MS) was used for tracking BPA and detection of intermediates. On this basis, we developed a computational model that successfully predicts temporal concentration profiles of all reactive species interacting with •OH, along with degradation kinetics across current densities (10–20 mA/cm²). By incorporating predictions from the Toxicity Estimation Software Tool (T.E.S.T.), the developed model accurately simulates time-dependent evolution of relative toxicity throughout the treatment process. The presented approach has a general character and requires rather simple experimental input to predict and optimize degradation outcome in terms of input concentration, degradation time, current density, and final toxicity. Further modifications of the model would enable widening to other EAOPs systems. Full article

Mineral carbonation is a prominent method for carbon sequestration. Atmospheric carbon dioxide (CO₂) is trapped as mineral carbonate precipitates, which are geochemically, geologically, and thermodynamically stable. Carbonate rocks can originate from biogenic or abiogenic origin, whereby the former refers to the breakdown of biofragments and the latter precipitation out of water. Carbonates can also be formed through biologically controlled mechanisms (BCMs), biologically mediated mechanisms (BMMs), and biologically induced mechanisms (BIMs). Microbial carbonate precipitation (MCP) is a BMM occurring through the interaction of organics (extracellular polymeric substances (EPS), cell wall, etc.) and soluble cations facilitating indirect precipitation of carbonate minerals. Microbially induced carbonate precipitation (MICP) is a BIM occurring via different metabolic pathways. Enzyme-driven pathways (carbonic anhydrase (CA) and/or urease), specifically, are promising for the high conversion to calcium carbonate (CaCO₃) precipitation, trapping large quantities of gaseous CO₂. These carbonate precipitates can trap CO₂ via mineral trapping, solubility trapping, and formation trapping and aid in CO₂ leakage reduction in geologic carbon sequestration. Additional experimental research is required to assess the feasibility of MICP for carbon sequestration at large scale for long-term stability of precipitates. Laboratory-scale evaluation can provide preliminary data on preferable metabolic pathways for different materials and their capacity for carbonate precipitation via atmospheric CO₂ versus injected CO₂. Full article

Systematically assessing the impact of industrial restructuring on carbon emissions and economic growth from the industrial correlation perspective holds great significance for realizing sustainable economic development. By extending the input–output analysis, this study developed a comprehensive assessment framework to evaluate the impacts of industrial restructuring on energy-related carbon emissions and economic growth within a multi-sectoral system from the industrial correlation perspective. An indicator system was established to identify key sectors for different industrial restructuring strategies. Taking Guangdong as a case, the results show that (1) the indirect impact of industrial restructuring in sectors such as equipment manufacturing and services on carbon emissions is more significant than that on economic growth, and the carbon intensity of its indirect impact is much larger than that of its direct impact; (2) industrial restructuring indirectly affects energy-related carbon emissions or economic growth mainly through a limited number of linked sectors, whereas the main linked pathways through which sector-specific industrial restructuring indirectly affects carbon emissions and economic growth are not consistent; (3) from the industrial correlation perspective, environmental benefits are higher for the service sector and lower for the construction sector; and (4) in industrial restructuring, the metal-processing sector is identified as a key sector for pursuing low-carbon transition, while the non-metallic mineral products sector is identified as a key sector for controlling production scale. The findings and framework can inform regional decisions on industrial restructuring and carbon reduction from the industrial correlation perspective. Full article

CO₂ emissions from fossil fuel combustion are the main source of anthropogenic greenhouse gases (GHGs). A method of reducing CO₂ emissions is CCUS (carbon capture, utilisation, and storage) technology. One part of CCUS technology involves mineral sequestration as its final stage, utilisation, which can be carried out using natural raw materials or waste. This is a particularly interesting option for power and CHP plants that use coal as their primary fuel. Combustion processes produce fly ash as a waste by-product, which has a high potential for CO₂ sequestration. Calcium fly ash from lignite combustion and fly ash from fluidised bed boilers have particularly high potential due to their high CaO content. Fly ash can be used in the mineral sequestration of CO₂ via direct and indirect carbonation. Both methods use CO₂ and flue gases. Studies conducted so far have analysed the influence of factors such as temperature, pressure, and the liquid-to-solid (L/S) ratio on the carbonation process, which have shown different effects depending on the ash used and the form of the process. Due to the large differences found in the properties of fly ash, related primarily to the type of fuel and boiler used, the process of mineral CO₂ sequestration requires much research into its feasibility on an industrial scale. However, the method is promising for industrial applications due to the possibility of reducing CO₂ emissions and, at the same time, recovering waste. Full article

Biochar is a carbon-rich material that has recently received attention due to its increasing agronomical potential. The agricultural utilization of biochar relates to its potential to act in the soil as a soil conditioner; nevertheless, complex information on the direct dependence of biochar’s physical properties (texture, particle size) and corresponding leaching and availability of organic molecules (e.g., the polycyclic and heterocyclic organic compounds) and inorganic mineral salts (based on micro- and macroelements) is still inconsistent. Multi-elemental analysis by using inductively coupled plasma atomic emission spectroscopy (ICP-OES) was used to assess the information on the contents and availability of macro- and microelements in studied commercial biochar samples. The results showed a statistically significant indirect relation between an increase in the size fraction of biochar and the content of aqueous-extractable K and Na and the direct relation with the aqueous-extractable Ca, Mg, and P. Compared to the macroelements, the detected contents of aqueous-extractable microelements were almost three orders lower, and the dependence on fraction size was not consistent or statistically significant. In addition, gas chromatography (GC) coupled with mass spectroscopy (MS) was further used to reveal the concentrations of available polycyclic aromatic and heterocyclic compounds in biochar samples. The detected concentrations of these types of organic compounds were far below the certified limits, and a statistically significant indirect correlation with particle size was also observed for all the studied biochar samples. The proposed methodological concept could provide the necessary insights into the description of biochar mineral content and its connection to biochar texture, the physicochemical properties, and the potential of biochar to release nutrients into the soil. These findings could help in the further assessment of biochar as a soil conditioner in modern agriculture. Full article

CCUS technologies are crucial solutions for mitigating climate change by reducing CO₂ emissions from industrial operations and energy sectors. This review critically examines the current state of CCUS technologies, and highlights advancements, challenges, regulatory frameworks, and future directions. It comprehensively analyzes carbon capture methods, such as pre-combustion, post-combustion, and oxy-fuel combustion capture, while comparing their efficiencies and limitations. The review also explores carbon utilization techniques, such as direct and indirect utilization, emphasizing their potential applications and technological constraints. Additionally, it assesses various carbon storage methods, focusing on geological, ocean, and mineralization storage, and discusses their capacity, feasibility, and environmental implications. The study reviews the policy and regulatory frameworks, economic viability, market trends, and environmental sustainability of CCUS. By identifying research gaps and recommending future research priorities, this review aims to guide the development of more efficient/effective, and cost-effective CCUS technology, ensuring their role in a sustaining low-carbon future. This review provides a forward-looking perspective, a critical and interdisciplinary analysis that assesses the current state of CCUS technologies, and further provides a roadmap for future development. Full article

Indirect combustion with the chemical looping combustion (CLC) of solid oxygen carriers is one of the most promising technologies for capturing carbon dioxide (CO₂) in energy production from fossil fuels since the separation of the generated CO₂ is inherent to the process itself. Therefore, the cost associated with capturing this gas will be significantly reduced. This technology transfers oxygen from air to fuel through a metal oxide that acts as an oxygen carrier, avoiding direct contact between air and fuel. This oxygen carrier circulates in a fluidized bed reactor called a reduction reactor and an oxidation reactor. (1) This research work has focused on evaluating the behavior of oxygen carriers based on the original and improved manganese mineral (copper-impregnated mineral) named for this study, OXMN009 and OXMN009P, respectively. (2) Equilibrium experiments were carried out on a thermogravimetric balance (TGA) to evaluate the kinetic behavior of these oxygen transporters OXMN009 and OXMN009P, using the gases methane (CH₄), carbon monoxide (CO), and hydrogen (H₂). (3) The enhanced solid oxygen carrier OXMN009P exhibited good performance for the CLC process with gaseous fuels in terms of reactivity and combustion efficiency, having high reactivity and oxygen transfer properties due to copper impregnation. (4) The results show that OXMN009P has comparable reactivity to other manganese-based materials reported in the literature. It may be an effective option for carbon dioxide capture, as it uses metal oxides as the oxygen transporters (TO). (5) These oxygen transporters, OXMN009 and OXMN009P, are used in a cyclic process that prevents the formation of nitrogen oxides by keeping the air and fuel separate. (6) Thermogravimetric balance (TGA) experiments were conducted to evaluate the kinetic behavior of these copper-modified oxygen transporters. (7) It was found that OXMN009P improved the reactivity and oxygen transfer properties due to copper impregnation. The kinetic parameters obtained in the TGA indicate that the reaction is non-thermal and requires less energy to initiate. (8) The results show that OXMN009P has reactivity comparable to other manganese-based materials reported in the literature and can be an effective option for carbon dioxide capture. Full article

The influences of legume diversification on soil carbon (C) pools and sequestration, particularly in Himalayan pastureland, remain poorly understood. Moreover, the impact of legume diversification activities and the stoichiometry of soil enzymes in C biogeochemistry at the ecosystem level remains largely overlooked. The purpose of this study is to investigate the influences of legume diversification on activities and the stoichiometry of soil enzymes and their control of C sequestration in pasturelands. Four experimental fertilized species combinations, namely, SG (50% Festuca arundinacea + 50% Dactylis glomerata), SGL1 (25% Festuca arundinacea + 25% Dactylis glomerata + 50% Onobrychis viciifolia), SGL2 (25% Festuca arundinacea + 25% Dactylis glomerata + 50% Trifolium pratense), SGL12 (25% Festuca arundinacea + 25% Dactylis glomerata + 25% Onobrychis viciifolia + 25% Trifolium pratense), and natural pasture (NG) were compared. Soils under SGL1, SGL2, and SG12 had ~18, 36, and 22% greater soil C than SG, respectively. Among the pastures with fertilization, the C mineralization was suppressed by legume diversification. C sequestration under SGL1, SGL2, and SG12 was ~27, 22, and 38% higher than SG, respectively, at the 0–30 cm soil layer. The ratios of DHA are as follows: for PhOX and DHA, PerOX significantly decreased with an increasing grass–legume mixture, suggesting greater C sequestration. PCA analysis revealed that C sequestration under legume diversification and enzymatic stoichiometry had an indirect but substantial impact on C sequestration. The increasing C sequestration under SGL12 was complemented by higher productivity. Data suggested that increasing legumes in pastureland might greatly enhance ecosystem functions such as soil C storage, productivity, ecorestoration efficiency, and biological activity in Indian Himalayan pastureland. Full article

Changes in soil nutrient dynamics after biochar application may affect indirect carbon sequestration through changes in plant productivity in forest ecosystems. In the present study, we examined the effects of woody biochar application on soil nitrogen (N) cycling over 8 months in a warm-temperate deciduous broad-leaved forest. Mineral soil samples were collected from the plots treated with different biochar applications (0, 5, and 10 Mg ha⁻¹), and the soil inorganic N concentration was measured. Net mineralization and nitrification rates were determined in each plot using the resin–core method. Soil temperature and water content did not change significantly, but the pH increased significantly following biochar application. Soil inorganic N concentrations (NH₄⁺ and NO₃⁻) and net N transformation rates (mineralization and nitrification rates) were significantly reduced. Microbial biomass and the nitrification ratio (the ratio of nitrification rate to mineralization rate) were unchanged, indicating that the decrease in soil inorganic N concentration was due to the reduced mineralization rate. Adsorption of substrates (from organic matter) by the applied biochar is the most likely reason for the reduction in the N mineralization rate. The results indicate that biochar application does not necessarily stimulate N transformation, which will affect indirect carbon sequestration. Full article

Mining waste is generated in vast quantities globally, which can have negative environmental consequences. This study highlights the utilization of iron ore mining waste as feedstock material in the preparatory step of an indirect aqueous mineral carbonation for carbon sequestration. The role of reactive cations (Ca²⁺, Mg²⁺, and Fe²⁺) was investigated in view of their elution behavior to improve carbonation efficiency. An elution experiment was carried out for the divalent cations using different acids (oxalic, HCl, acetic, and formic acid) at different concentration solutions (up to 1.5 M) and times (up to 100 min) at ambient temperature. The initial analysis confirmed the presence of divalent cations in the sample. The elution approach at ambient temperature resulted in the elution efficiency of Fe²⁺ (30.4%), Mg²⁺ (54%) using oxalic acid, and Ca²⁺ (98%) using HCl at a relatively short time between 50 and 100 min. It was found that for the iron ore mining waste, oxalic acid and HCl were best suited as elution agents for the Fe²⁺ and Mg²⁺, and Ca²⁺, respectively. The CO₂ sequestration potential was calculated to be 131.58 g CO₂/kg residue. A further carbonation step using a complexing agent (1,10 phenanthroline) confirmed the formation of siderite and magnesite along with phenanthroline hydrates. Findings have shown that the indirect mineral carbonation of the iron mining waste with complexing agent might improve carbonation efficiency, thus indicating that this material is useful for long-term carbon capture and storage applications. Full article

Carbon sequestration in agricultural soils, through the accumulation of high-quality organic matter, represents great potential to mitigate climate change and simultaneously improve soil fertility. Such a challenge is particularly important and relevant in developing tropical countries like Madagascar, where soil carbon storage is vulnerable to climatic variations and where fertilization is generally applied through amendments in organic matter of various origins. The priming effect (PE) is considered here as the stimulation of the mineralization of soil organic matter (SOM) by a supply of fresh organic matter (FOM). PE results from different microbial processes driven by specific biotic and abiotic parameters. Depending on the processes involved, it has been suggested that PE could either counteract SOM accumulation or promote it. The objective of the present study was to explore the relationships between certain agricultural practices (type of crop, quality of fertilization, association with trees), the potential intensity of PE, as well as several abiotic (texture, quantity and quality SOM, nutrient enrichment) a1nd biotic (biomass and phylogenetic composition of microbial communities) factors which have been proposed in the literature as specific determinants of the different PE generation mechanisms. The soils for this study come from a network of farms in a commune in the Highlands of Madagascar. The PE, generated by a supply of ¹³C-enriched wheat straw, could not directly correlate with agricultural treatments. However, several indirect correlations could be found via several specific abiotic and microbial determinants that are discussed in terms of soil fertility restoration. Full article

Coal fly ashes (COFA) are readily available and reactive materials suitable for CO₂ sequestration due to their substantial alkali components. Therefore, the onsite collaborative technology of COFA disposal and CO₂ sequestration in coal-fired power plants appears to have potential. This work provides an overview of the state-of-the-art research studies in the literature on CO₂ sequestration via the mineralization of COFA. The various CO₂ sequestration routes of COFA are summarized, mainly including direct and indirect wet carbonation, the synthesis of porous CO₂ adsorbents derived from COFA, and the development of COFA-derived inert supports for gas-solid adsorbents. The direct and indirect wet carbonation of COFA is the most concerned research technology route, which can obtain valued Ca-based by-products while achieving CO₂ sequestration. Moreover, the Al and Si components rich in fly ash can be adapted to produce zeolite, hierarchical porous nano-silica, and nano-silicon/aluminum aerogels for producing highly efficient CO₂ adsorbents. The prospects of CO₂ sequestration technologies using COFA are also discussed. The objective of this work is to help researchers from academia and industry keep abreast of the latest progress in the study of CO₂ sequestration by COFA. Full article

As objects for reforestation, the least studied are carbonate substrates, which have a number of specific features in terms of mineral composition, the exchange of nutrients, and biological activity. The use of biological preparations of a consortium of bacteria of the genus Bacillus and mycorrhizal fungi of the genus Glomus in growing seedlings of Scots pine (Pinus sylvestris L.) on carbonate substrates provides the metabolic products; soluble and microelement salts function as catalysts for chemical reactions of exudates and soil products; and a greater amount of plant heavy metals (HM) Cu, Zn, Cd, and Pb accumulate in the soil. Among HMs, the random factors most strongly determined an accumulation of Cd (the influence rate of random factors h²_x = 34.6%) and Pb (the influence rate of random factors h²_x = 21.7%) in the plants. A trend of all studied HMs higher uptake by the Cretaceous pine (Pinus sylvestris var. cretacea (Kalen.) Kom.) in comparison with the P. sylvestris ecotype is revealed. Against the biological preparation background of Biogor KM and MycoCrop^®, a greater value of the HM’s biological absorption in comparison with the option without biological preparations is noted. This process occurs against a background of a significant increase in the nitrification capacity in the chalk fine-grained substrate (soil aggregates < 1 mm in size), which is an indirect indicator of an increased intensity of microbiological processes. Spearman’s correlation was noted between the coefficient of accumulation of Cu, Zn, Cd, and Pb in the dry matter of Scots pine (P. sylvestris) seedlings and the nitrification capacity of substrate (r_s = 0.610–0.744, p < 0.05), as well as the relationship between the nitrification capacity index of substrate and the coefficient of biological absorption of copper, zinc, and cadmium (r_s = 0.543–0.765, p < 0.05). No relationship was found between the coefficient of biological absorption of lead and other soil chemical property indicators. HM absorption by plants was random. No correlations have been established between an accumulation of HMs and a content of total nitrogen, an absolute value of nitrate nitrogen, a humus content, or a pH. The significance of the work is the possibility of providing reliable reforestation with Scots pine (P. sylvestris) and Cretaceous pine (P. sylvestris var. cretacea) on the chalk outcrops using the biological preparations Biogor KM, MycoCrop^®, and BGT* methodology and ensuring soil phytoremediation from HMs. Full article