Search Results (236)

The conventional pyrolysis of tar-rich coals faces limitations in maximizing tar yield and optimizing tar composition, often resulting in inefficient resource utilization and elevated emissions of CO₂. This study investigates a novel cryogenic pretreatment method using liquid nitrogen to enhance pyrolysis efficiency, aiming to improve tar yield and transform tar quality for sustainable coal utilization. Three tar-rich coals underwent cryogenic pretreatment at varying temperatures (0 to −90 °C) via liquid nitrogen, followed by pyrolysis. The product distribution (tar, gas) and quality were analyzed and compared to conventional pyrolysis and the Gray–King assay. The cryogenic pretreatment increased the tar yield by 25.8–44.6% compared to conventional methods, achieving a maximum yield of 7.8–16.0 wt% at −90 °C. The emissions of CO₂ decreased by 12.7–27.4%, while CH₄ and H₂ proportions rose by 15.1–60.2%, enhancing gas energy content. The pretreatment reduced benzene compounds by 4.4–13.9 wt% and increased aromatic derivatives by 13.9–20.5 wt%, indicating a shift toward higher-value chemicals. The cryogenic approach demonstrates the dual benefits of boosting tar productivity while reducing carbon emissions, offering a promising path for cleaner and more efficient coal pyrolysis. Full article

Extensive and unregulated groundwater extraction for irrigation in the arid inland basins of Northwest China has led to a continuous increase in groundwater depth in agricultural irrigation areas. This has significantly altered the distribution of soil ions, making it difficult to predict their evolution and dynamic patterns. In this study, we used a space-for-time substitution approach to elucidate the evolution of the soil ion distribution under changing groundwater depths. Experiments were conducted in three typical irrigation areas with varying groundwater depths, that is, below 5 m, 5–10 m, and above 10 m in Korla, Xinjiang, China. Soil samples were collected from five profiles at depths of 0–180 cm to measure the soil moisture, salinity, and major ion content. An innovative research framework was developed to examine the relationship between groundwater depth and soil ion distribution using ion ratios, principal components, hierarchical clustering, and correlation analyses. This framework aims to reveal the dynamics, correlations, and mechanisms of soil moisture, salinity, ion distribution, and representative ion composition as groundwater depth increases in the arid agricultural irrigation areas of Northwest China. The results showed that as groundwater depth increased, the soil chemical type shifted from Ca-SO₄ to Na-SO₄ and mixed types, with an increase in SO₄²⁻ and Na⁺ content in the soil profile. Soil moisture, salinity, sodium adsorption ratio (SAR), and total dissolved solids (TDS) were significantly higher in shallow groundwater than in deep groundwater. Groundwater depth was negatively correlated with soil moisture, salinity, and major cations and anions (K⁺, Na⁺, Ca²⁺, Mg²⁺, Cl⁻, SO₄²⁻, and NO₃⁻). Meanwhile, a positive correlation exists between groundwater depth and CO₃²⁻. The dynamic distribution of soil ions is primarily governed by groundwater depth and is influenced by multiple factors. Evaporation is the dominant factor in shallow groundwater areas, whereas the mineral composition of rocks plays a crucial role in deep groundwater areas. These findings provide scientific support for strategic agricultural water-resource management policies and sustainable development strategies in arid regions. Full article

Graphene oxide (GO), a pivotal derivative of graphene, has revolutionized nanotechnology with its tunable physicochemical properties and interdisciplinary applications in energy storage, environmental remediation, and biomedicine. Despite its exponential research growth, existing reviews remain fragmented, lacking holistic insights into evolving synthesis–application linkages, global collaboration patterns, and emerging convergence trends. This study bridges these gaps through a scientometric analysis of 14,124 peer-reviewed articles (2022–2025) from the Web of Science Core Collection, utilizing CiteSpace for co-occurrence network mapping, burst detection, and cluster analysis. Key findings reveal (1) a thematic shift from traditional synthesis optimization (e.g., Hummers’ method) toward driven material design and sustainable applications like GO membranes for water purification; (2) China’s dominance in publication output (38.5%) contrasts with the U.S. and Europe’s leadership in global collaborations; (3) interdisciplinary journals such as Chemical Engineering Journal (centrality: 0.25) and emerging clusters like “circular economy” signal transformative priorities; and (4) critical gaps in scalability, ecological safety, and cost-effective production hinder industrial translation. This work provides a roadmap for aligning research with sustainability goals, fostering global partnerships, and accelerating innovations in scalable nanotechnology. Full article

In response to the growing demand for high-performance materials in industries such as automotive, aerospace, and construction, this study investigates the impact of jute cellulose nanofibers (CNFs) on the chemical, thermal, and morphological properties of thermoplastic polyurethane (TPU) nanocomposites. Jute CNFs were extracted using a chemo-mechanical method and incorporated into TPU through melt blending. Fourier transform infrared (FTIR) spectroscopy revealed notable changes in the chemical structure of the nanocomposites, including intensified O-H stretching vibrations and reduced C-H stretching vibrations upon the addition of 2 wt% and 4 wt% jute CNFs. Strong interfacial interactions between the jute CNFs and the TPU matrix were observed, particularly influencing the absorbance bands related to the -NH, C=O, and N-H groups. X-ray diffraction (XRD) analysis demonstrated enhanced crystallinity in the TPU nanocomposites, with new diffraction peaks and increased crystallite size correlating with higher jute CNF content. Field emission scanning electron microscopy (FESEM) revealed a uniform dispersion of the jute CNFs within the TPU matrix, contributing to improved interfacial adhesion and enhanced structural integrity. Thermal analysis using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) showed an increase in the thermal stability, with the onset of degradation occurring at higher temperatures in the TPU/jute CNF nanocomposites. The glass transition temperature (T_g) and melting temperature (T_m) exhibited minor shifts, reflecting improved thermal performance. These findings suggest that the incorporation of jute CNFs significantly enhances the crystallinity, thermal stability, and structural organization of TPU, offering a sustainable approach for developing robust materials with potential applications in structural, corrosion-resistant, and high-performance fields. Full article

In this study, we comparatively discuss chemical and isotopic characteristics of thermal waters from several geothermal fields within the eastern part of the Büyük Menderes graben, Western Türkiye. The studied thermal waters with a wide range of temperature (33 to 242 °C) and pH value (6.10 to 9.38) show water types varying from Ca-Mg-HCO₃-SO₄ to Na-HCO₃-SO₄. The chemical composition of waters is controlled by several processes, which include temperature, circulation depth, extent of water–rock interaction, dissolution/precipitation, mixing, cation exchange and microbial activity. All thermal waters are of meteoric origin and generally have deep circulation. δ¹³C data indicate that marine limestone and mantle-derived CO₂ are the major sources of carbon in thermal waters and δ³⁴S values imply that the sulfate is originated from the Neogene gypsums. At discharge temperatures, all thermal waters are saturated with various carbonate, silica and clay minerals, which is supported by the XRD analysis of scaling materials. The REY composition of the scaling samples showed that the limestone is the source rock for the rare earth elements. Thermal waters with a positive ¹⁸O shift of 2.7 to 4.6‰ have reservoir temperatures of 170–245 °C, whilst other waters with a shift of <1‰ have reservoir temperatures in the range of 79 to 166 °C. Regarding the distribution of temperature, electricity production seems to be more suitable in the western part of the region, although relatively low-temperature areas in the east also look promising. Full article

The initial variations in soil bacteria at the very beginning of reclamation still remains unclear. This study investigates the impact on bacterial communities of eight different treatments, including uncultivated land, unfertilized cultivation, chemical fertilizer, chemical fertilizer + bacterial fertilizer, manure, manure + bacterial fertilizer, manure + chemical fertilizer, and manure + chemical fertilizer + bacterial fertilizer, during the short-term reclamation of coal-mining soils. The results showed that total nitrogen, available phosphorus, soil organic carbon, microbial biomass carbon, and alkaline phosphatase activity were significantly increased in all fertilization treatments compared to uncultivated land (p < 0.05). All fertilization treatments other than chemical fertilizer harbored significantly higher activities of urease, catalase, and invertase than unfertilized cultivation (p < 0.05). The bacterial communities structures in manure-amended treatments significantly differed in uncultivated land and unfertilized cultivation and were phylotypically shifted from oligotrophic to Actinobacteria-dominant copiotrophic traits, accompanied with phenotypic succession of the enriching characteristics of Gram-positive, biofilms formation, and stress tolerance. The co-occurrence network in manure-amended treatments harbored a simple co-occurrence network, indicating more productive soils than in no-manure treatments. Manure amendment, total nitrogen, microbial biomass carbon, invertase, catalase, and soil moisture were the key driving factors. Our study underscores the bacterial initialization characteristics promoted by manure at the very beginning of coal-mining reclamation. Full article

The chemical structure of coal is very composite, consisting of a heterogeneous carbonaceous matrix with variable degrees of “turbostratic” order and the inclusion and/or exclusion of mineral matter (ash). The formation of surface oxides on carbon has long been recognized as a key to understanding many chemical and physical properties of carbon materials relevant to their consolidated or emerging applications. The extent and nature of surface oxides can effectively be assessed by high-resolution X-ray photoelectron spectroscopy (XPS), which provides excellent insight into the functional nature of C-O moieties. However, the XPS analysis of ash-bearing carbons may be biased by the interfering effects of inorganics with the most relevant spectral ranges, namely the core levels O_1s and C_1s. The effect of ash components on the spectroscopic characterization of carbon is scrutinized here with reference to a sub-bituminous coal characterized by a fairly large ash content. The coal is subjected to different treatments, including devolatilization, milling, and oxidation. A synthetic carbon (Carboxen) is used as a reference sample for the correct assignment of the carbon–oxygen functionalities in the core-level XPS spectra (C_1s and O_1s) in the absence of mineral matter. On the opposite side, fly ash from an industrial coal boiler is analyzed to investigate the effects of mineral matter. It is shown that the establishment of non-uniform charging of the sample induced by ash provides a key to the interpretation of the XPS spectra of ash-bearing carbon samples. The positive charge on the surface, referred to as the charging effect, brings about a shift of the core-level binding energies towards higher values. Grinding of the samples or partial combustion emphasizes the charging effect. XPS analysis of the fly ash, where carbon is largely consumed and dispersed in the inorganic matter, confirms that charging arises from non-conductive aluminosilicates. These effects may induce remarkable changes in carbon and oxygen peak shapes and need to be accounted for to obtain correct interpretations of the XPS spectra of ash-rich carbonaceous fuels. Full article

Currently, solid waste storage systems generate secondary pollutants such as leachates, derived from rainwater infiltration or produced during their storage, which affect water quality, human health, and the environment. This study evaluated a bioremediation system for leachates from the “Rancho Triste” landfill using Spirulina sp. as a microalgal strain. Its rapid adaptation to the leachate was identified through respirometry based on CO₂ measurement, allowing the modeling of microalgal adaptation using a Log-Normal Peak Shifted with Offset function. Tests conducted in a 0.5 L reactor determined an optimal treatment time of 10 days, achieving removals of 87.17% for iron, 28.96% for magnesium, and 90.74% for manganese. Subsequently, a 2³ factorial design was implemented to optimize the reduction of chemical oxygen demand (COD), evaluating agitation, lighting, and nitrogen supplementation, achieving a COD removal efficiency exceeding 50% under optimal conditions. The fed-batch technique enabled an enrichment of microbiological populations, which, together with bio-stimulation, bioventilation, and photoperiods, demonstrated the scalability of the bioprocess and the significant reduction of metallic and recalcitrant contaminants present in the leachate. This approach proposes an ecological alternative with potential application in water treatment industries aiming for carbon neutrality and optimal transformation of high-effluent volumes. Full article

Chile holds ~50% of temperate forests in the Southern Hemisphere, thus constituting a genetic–ecological heritage. However, intense anthropogenic pressures have been inducing distinct forest structural-regeneration patterns. Accordingly, we evaluated 22 soil properties at 0–5 and 5–20 cm depths in two protected sites, with similar perturbation records but contrasting post-disturbance regeneration stages: long-term secondary forest (~50 y) (SEC_FORST) (dominated by Chusquea sp.-understory) and a short-term forest after disturbance (~5 y) (FAD_IST) within a Nothofagus spp. forest to determine the potential of these soils to promote nutrient availability, water cycling, soil organic carbon (SOC) sequestration (CO₂→SOC), and microbiome. Results detected 93 correlations (r ≥ 0.80); however, no significant differences (p < 0.05) in physical or chemical properties, except for infiltration velocity (+27.97%), penetration resistance (−23%), SOC (+5.64%), and % Al saturation (+5.64%) relative to SEC_FORST, and a consistent trend of suitable values 0–5 > 5–20 cm were estimated. The SOC→CO₂ capacity reached 4.2 ± 0.5 (FAD_IST) and 2.7 ± 0.2 Mg C y⁻¹ (SEC_FORST) and only microbial abundance shifts were observed. These findings provide relevant insights on belowground resilience, evidenced by similar ecosystem services provision capacities over time, which may be influenced progressively by opportunistic Chusquea sp. Full article

The conversion of carbon dioxide into fuels and fine chemicals is a highly desirable route for mitigating flue gas emissions. However, achieving selectivity toward olefins remains challenging and typically requires high temperatures and pressures. Herein, we address this challenge using 12 nm copper nanoparticles supported on FeOx micro-rods, which promote the selective hydrogenation of CO₂ to light olefins (C₂–C₄) under atmospheric pressure. This catalyst achieves up to 27% conversion and 52% selectivity toward C₂–C₄ olefins, along with the production of C₂–C₄ paraffins, C₅+ hydrocarbons (with all C₁₊ products totalling to up to about 75%), and methane, while suppressing CO formation to just 1% at 340 °C. The enhanced performance of the Cu/FeOx pre-catalyst is attributed to the efficient in situ generation of iron carbides (Fe₅C₂) in the presence of copper nanoparticles, as confirmed by ex situ XRD analysis. Copper facilitates the reduction of FeOx to form Fe₅C₂, a crucial intermediate for shifting the reaction equilibrium toward higher hydrocarbons. The hydrogenation of CO₂ to higher hydrocarbons proceeds through the reverse water–gas shift reaction coupled with Fischer–Tropsch synthesis. Full article

The use of plastic agricultural mulching films presents a “double-edged sword”: while these films enhance crop yields, they also lead to the accumulation of plastic film residues in the soil, creating new pollutants (microplastics). Our understanding of the “plastisphere”, a niche formed by agricultural film residues in the soil, where unique microbial communities and soil conditions converge remains limited. This is particularly true for protists, which are recognized as key determinants of soil health. Therefore, this study simulated a field experiment to analyze the effects of long-term plastic film residues on the structure of protist microbial communities in the rhizosphere, bulk soil and plastisphere of oilseed rape as well as their effects on soil nutrients. The results revealed that the residual plastic films underwent significant structural and chemical degradations. Protist diversity and co-occurrence network complexity were markedly reduced in plastisphere soils. In addition, soil moisture content, inorganic nitrogen and available phosphorus levels declined, leading to deficiencies in soil nutrients. Functional shifts in consumer protists and phototrophs along with weakened network interactions, have been identified as key drivers of impaired nutrient turnover. Our study underscores the critical role of protist communities in maintaining soil nutrient cycling and highlights the profound adverse effects of plastic film residues on soil ecosystems. These findings provide valuable insights into mitigating plastic residue accumulation to preserve long-term soil fertility and ensure sustainable agricultural productivity. Full article

Excessive (carbon dioxide) CO₂ emissions are a primary factor contributing to climate change. As one of the crucial technologies for alleviating CO₂ emissions, carbon capture and utilization (CCU) technology has attracted considerable global attention. Technologies for capturing CO₂ in extreme circumstances are indispensable for regulating CO₂ levels in industrial processes. The unique separation characteristics of the ceramic–carbonate dual-phase (CCDP) membranes are increasingly employed for CO₂ separation at high temperatures due to their outstanding chemical, thermal durability, and mechanical strength. This paper presents an overview of CO₂ capture approaches and materials. It also elaborates on the research progress of three types of CCDP membranes with distinct permeation mechanisms, concentrating on their principles, materials, and structures. Additionally, several typical membrane reactors, such as the dry reforming of methane (DRM) and reverse water–gas shift (RWGS), are discussed to demonstrate how captured CO₂ can function as a soft oxidant, converting feedstocks into valuable products through oxidation pathways designed within a single reactor. Finally, the future challenges and prospects of high-temperature CCDP membrane technologies and their related reactors are proposed. Full article

Silica aerogels are extensively used as catalyst supports due to their mesoporous structure and chemical inertness. In this study, SiO₂–AuNP aerogels containing gold nanoparticles (AuNPs) were synthesized using the sol-gel method followed by supercritical CO₂ drying. The inclusion of polyvinyl pyrrolidone (PVP) as a stabilizing agent preserved the gold particle sizes during the gelation process. In contrast, aerogels synthesized without PVP contained enlarged AuNP aggregates, resulting in a shift in the plasmon resonance color from red to bluish or blue–grey. Thermal treatment of these bluish-colored aerogels at high temperatures restored their red coloration, visually indicating the breakdown of large gold clusters into individual nanoparticles. Both types of aerogels were characterized using SEM, TEM, 3D optical microscopy, UV–vis and ATR-IR spectroscopy, and N₂ porosimetry, with their properties analyzed as a function of annealing temperature. Their catalytic activity was evaluated through the reduction of 4-nitrophenol with sodium borohydride, and both aerogel types demonstrated catalytic activity. This thermal conversion of large clusters into individual nanoparticles within an aerogel matrix introduces a new and promising approach for creating catalytically active nanogold-containing aerogel catalysts. Full article

In this study, the homogeneous carboxylation of potassium, sodium, and lithium phenolates in DMSO solution at 100 °C by the Kolbe–Schmitt reaction was investigated. The impact of water, phenolate concentration, and cation nature on the yield of products and reaction selectivity was demonstrated. Based on the patterns observed, it was concluded that a complex cluster mechanism governs the carboxylation reaction in the solution. The use of a homogeneous reaction medium allowed for convenient testing of various additives to assess their impact on the reaction. Basic additives such as sodium salts of mesitol, tert-butylcalix[4]arene, sodium isopropyl, and tert-butyl cabonates were found to enhance the reaction, increasing the yield of hydroxybenzoic acids by 20% (to 61.6%). The main product in the DMSO solution was identified as 4-hydroxybenzoic acid, in contrast to the classical Kolbe–Schmitt method which typically yields 2-hydroxybenzoic (salicylic) acid. The use of ¹³C NMR spectroscopy enabled the observation of a “carbonate complex” in the solution for the first time, with the carbonate carbon displaying a chemical shift value of 142 ppm, an unusual finding for stable carbonates, and located between the signals of free dissolved CO₂ and carboxylate derivatives. Full article

In situ measurements of the chemical identity and quantity of anode gases during electrochemical measurements and rare earth (RE) electrolysis from fluoride-based molten salts composed of different kinds of rare earth oxides (REOs) were performed using FTIR spectrometry. Linear sweep voltammetry (LSV) was carried out to characterize oxidation processes and determine the anodic effect from NdF₃ + PrF₃ + LiF + REO melt. RE complex formation and subsequent reactions on the GC anode surface were discussed to understand the formation pathways of CO/CO₂ and perfluorocarbon gases (PFC), mainly CF₄ and C₂F₆. The LSV shows that increasing the REO content from 1 wt.% up to 4 wt.% in the system, leads to a positive shift in the critical potential for a full anode effect, recorded around 4.50 V vs. W with 4 wt.% REO. The FTIR results from on-line off-gas analysis during LSV measurements indicate that the anode gas products were composed mainly of CO and CO₂, whereas CF₄ can be detected before the full anode effect and C₂F₆ at and after this phenomenon. Compositions of off-gases from electrolysis performed using different kinds of REOs were compared. The main off-gas component was found to be CO in RE electrolysis with REOs as raw materials, while in electrolysis with magnet recycling derived oxides (MRDOs), CO₂ content was slightly higher compared to CO. PFC emissions during RE electrolysis were generally similar: CF₄ was detected periodically, but in negligible concentrations, while C₂F₆ was not detected. Full article