Search Results (1,859)

In this study, chicken bone biochar (CBC) was prepared from waste chicken bones via oxygen-limited pyrolysis. A magnetic component (Fe₃O₄) was introduced, and the composite was embedded in a sodium alginate (SA) gel network, successfully constructing magnetic chicken bone biochar/sodium alginate composite gel beads (M-CBC/SA). The experimental results showed that under the conditions of pH = 4.5, 25 °C, and an adsorbent dosage of 0.5 g/L, the removal efficiency of M-CBC/SA toward 50 mg/L U(VI) reached 91.67%, corresponding to an adsorption capacity of 91.67 mg/g. The adsorption process followed the pseudo-second-order kinetic model and the Langmuir isotherm model, with a theoretical maximum adsorption capacity of 322.58 mg/g, indicating that the adsorption was dominated by monolayer chemisorption. The material exhibited excellent magnetic separability and good anti-interference ability against coexisting ions such as K⁺, Na⁺, Cl⁻, and SO₄²⁻, and its adsorption behavior was only weakly affected by ionic strength. Characterization by XRD, FTIR, XPS, SEM-EDS and other techniques revealed that the immobilization mechanism of U(VI) involved the synergistic effects of dissolution–precipitation (the formation of a new autunite phase), surface complexation (involving hydroxyl and phosphate groups), ion exchange (exchange with Ca²⁺), and electrostatic attraction. Using waste chicken bones as the raw material, this composite achieves both efficient uranium immobilization and convenient magnetic separation, fully embodying the environmental concept of “treating waste with waste”, and shows promising application prospects in the treatment of uranium-containing wastewater. Full article

Conventional titanium alloy production based on the Kroll process features high energy consumption and long procedures, making low-cost, short-process fabrication a research focus in titanium metallurgy. In this work, low-interstitial γ-TiAl alloys were prepared via a coupled self-propagating high-temperature synthesis (SHS)–slag washing refining–vacuum arc remelting (VAR) process using TiO₂ as the raw material. Slag washing refining was performed at 1750 °C with 150 g of CaO-Al₂O₃-SiO₂-CaF₂ mold flux and 1.5 wt.% Ca, followed by VAR under a vacuum of 10⁻²–10⁻³ Pa. γ-TiAl alloy with a composition of Ti 66.01 ± 0.5 wt.%, Al 33.8 ± 0.5 wt.%, O 0.054 ± 0.002 wt.%, N 0.046 ± 0.005 wt.%, and C 0.085 ± 0.008 wt.% was obtained, and the inclusion size was refined to 0–3 μm. This coupled approach provides a scalable, low-cost route for the industrial preparation of low-interstitial γ-TiAl alloys. Full article

The inefficient utilization of industrial by-product phosphogypsum, coupled with the increasing global demand for cooling, has spurred the development of sustainable radiative cooling materials. Compared with conventional cooling coatings that primarily rely on expensive synthetic materials or complex fabrication processes, this study provides a promising cost-effective and sustainable route for integrating industrial solid waste valorization with zero-energy cooling technologies. In this study, we fabricated a composite coating (β-HPG@CA/SiO₂@OTS) consisting of β-hemihydrate phosphogypsum (β-HPG), a derivative product of phosphogypsum, cellulose acetate (CA), SiO₂ particles and octadecyltrichlorosilane (OTS) by a facile combination of blade coating and spraying, which exhibited strong solar reflectivity (90.9%), high mid-infrared emissivity (98.7%) and satisfactory superhydrophobicity (157°). The as-prepared composite achieved an ambient temperature drop of 18.7 °C under direct sunlight during sunny weather, achieving a net cooling power of 92.23 W/m². Meanwhile, the composite coating exhibits excellent durability after prolonged immersion in strongly acidic and alkaline solutions, ultraviolet radiation and outdoor testing. Owing to its simple fabrication process and robust cooling performance, this coating shows promise for scalable production and practical outdoor applications, such as building envelopes and equipment enclosures. Full article

Coal gangue (CG) ranks among China’s most significant industrial solid by-products. In response to China’s carbon neutrality commitments and the growing emphasis on resource recycling, finding effective ways to valorize CG has emerged as a pressing concern. Based on the mineral composition and chemical composition characteristics of CG, this study systematically investigated the enhancement effects of three alkali activators (Na₂SiO₃, NaOH, and Ca(OH)₂) on the cementitious properties of CG. Through different dosage and compressive strength tests, the efficiency ranking of the three activators was determined as follows: Na₂SiO₃ > Ca(OH)₂ > NaOH. A 10% Na₂SiO₃ dosage combined with 28-day curing was identified as the optimal condition for achieving sufficient reaction and structural densification. Under these conditions, the compressive strength of CG cementitious material reached 6.4 MPa, representing an increase of 190.9% compared to the blank group (2.2 MPa), significantly superior to Ca(OH)₂ (69.55%) and NaOH (62.27%). X-ray diffraction (XRD) and scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) analyses revealed that alkali activators function primarily by disrupting the crystalline framework of CG, promoting the cross-linking polymerization of silicon–aluminum monomers to generate dense cementitious products, thereby improving material performance. The Na₂SiO₃ is attributed to its “dual activation effect”, providing OH⁻ to create an alkaline environment while supplying reactive silicate ions (SiO₃²⁻) to accelerate N-A-S-H gel and C-A-S-H gel formation. These findings offer guidance for optimizing CG-based cementitious formulations for formula optimization and large-scale utilization of CG cementitious materials. Full article

Phase formation characteristics during the thermochemical reduction of metals from natural coltan using aluminum and calcium–aluminum alloy at 1400–1450 °C were investigated to develop methods for extracting niobium and tantalum from rare metal raw materials. The studied coltan sample consists of a columbite–tantalite solid solution with the composition (Mn,Fe)(Nb,Ta)₂O₆, cassiterite Sn_0.9O₂, tapiolite (Ta,Nb)₂(Mn,Fe)O₆, and calcioolivine Ca₂SiO₄. This study established that the choice of reducing agent determines the sequence of oxide phase transformations. During the aluminothermic process, orthorhombic columbite–tantalite is completely reduced, while tetragonal tapiolite persists even at 1400 °C. The use of a calcium–aluminum alloy containing 69.4 wt.% Ca results in a reversal of this trend: tapiolite is reduced at the early stages (800–1250 °C) through an intermediate (Ta,Nb)O₂ phase, whereas the columbite–tantalite solid solution remains up to 1250 °C. Calcium, having a high affinity for oxygen, forms intermediate perovskite-type oxide phases that act as diffusion barriers, limiting the access of the reducing agent to residual mineral inclusions (mainly Nb-Ta minerals of the orthorhombic crystal system). A temperature rise to 1450 °C initiates the redistribution of oxide components: the content of CaNbO₃ decreases, the Ca₂(Nb,Ta)AlO₆ phase disappears, and its components are involved in the formation of Ca(Nb,Ta)_0.25MnO_2.74 and Ca₄Nb₂O₉. Diffusion constraints are reduced, and the residual columbite–tantalite solid solution is reduced, as confirmed by its complete absence in the products at 1450 °C. In the metallic phase, solid solutions of tantalum and niobium, Ta-Nb-Sn intermetallic compounds (Ta,Nb)₃Sn, titanium aluminide, and ferroalloys with an increased (Ta,Nb)/(Fe,Mn) ratio are formed. The phase transformations elucidated during metallothermic reduction of coltan using different reducing agents, together with the formation of metallic and intermetallic phases, establish a scientific foundation for the development of advanced rare metal extraction processes. Full article

Telomerase reverse transcriptase subunit (TERT) is a key factor involved in telomere maintenance and genome stability, and the decline in its expression is closely related to cellular senescence. In this study, we established TERT monoallelic knockout (TERT+/−) and TERT overexpression (TERT-Over) cell lines in porcine iliac artery endothelial cells (PIEC) using CRISPR/Cas9 and PiggyBac systems to compare the effects of TERT monoallelic knockout versus overexpression on cellular biology. TERT expression and telomere length were assessed via qPCR and Western blot analysis. Cellular proliferation and senescence were evaluated using CCK-8 assays, cell cycle analysis, and SA-β-gal staining. Furthermore, the expression of key genes involved in cell proliferation, metabolism, and related signaling pathways was quantified using q-PCR. The results showed that the TERT mRNA level and telomere length decreased in TERT+/− cells. Meanwhile, we also observed that TERT+/− cells exhibited G1 phase arrest in the cell cycle, with suppressed proliferation and increased SA-β-gal-positive cells. This was accompanied by downregulation of cell cycle and proliferation-related genes, including c-Myc, the E2F family, and Ki-67, as well as downregulation of cell metabolism-related genes, including HIF1α, HK2, GLUT1, the SMAD family, FOXO1, and ATF4. In addition, cytochrome C was downregulated, suggesting activation of mitochondrial apoptotic signaling. Together, these findings indicate impaired proliferative and metabolic activity and are consistent with cellular senescence associated with telomere shortening. In TERT-overexpressing cells, the TERT gene expression and telomere length increase, cell proliferation accelerates, and the survival rate significantly increases under H₂O₂ treatment. This indicated that the overexpression of TERT can enhance resistance to oxidative stress, thus showing a kind of anti-aging phenotype. In conclusion, TERT monoallelic knockout induces cellular senescence-associated phenotypes in porcine endothelial cells, whereas TERT overexpression enhances proliferation and resistance to oxidative stress under the experimental conditions used in this study. The two porcine cell models established here may provide useful experimental materials for studying aging-related mechanisms and evaluating anti-aging interventions in large animals. Further studies are needed to directly determine their effects on cellular replicative lifespan. Full article

Brazilian soils are prone to a gradual decline in fertility due to intensive agricultural activity combined with natural weathering, which increases the demand for chemical fertilizers. Among potential alternatives, soil remineralization using crushed rock is a promising strategy. Silicate agrominerals (SAs) applied as soil remineralizers have attracted attention due to their ability to supply plant-available nutrients while reducing dependence on conventional mineral fertilizers. This study evaluated the potential of residues from six quarries in Brazil as soil remineralizers as a regulatory screening assessment. Samples were subjected to mineralogical, petrological, and chemical characterization using an integrated approach, including X-ray diffraction (XRD), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), and leaching experiments. XRD analysis revealed that anorthite and augite were the major minerals present in the mining waste. These minerals are less resistant to weathering, which enhances the release of macro- and micronutrients, essential for the development of various crops. Chemically, the samples were dominated by SiO₂, Fe₂O₃, and Al₂O₃, with the sum of bases (K₂O + CaO + MgO) ranging from 11.92% to 16.85%, meeting Brazilian standards for use as a soil remineralizer. Leaching results revealed that pH responses varied significantly among the studied samples for the filler particles, with an alkaline shift reaching values above 9.0 after 72 h. In contrast, the powder particle size samples showed no significant variation between the different materials tested, maintaining nearly constant pH levels throughout the period. This preliminary evaluation demonstrates that mining tailings from Brazilian quarries have potential as a sustainable soil remineralizer. This approach not only offers an alternative for soil fertilization but also promotes waste management and circular economy practices, although further studies are needed to assess long-term effectiveness and safety. Full article

Background and Objectives: Patients with rheumatoid arthritis (RA) are found to have a higher risk of dental diseases. Although herbal medicines (HMs) have long been used to treat various conditions, few studies focus on its impact on dental diseases. In this longitudinal cohort study, we assessed the correlation between HM use and risk of dental diseases in RA groups. Materials and Methods: A total of 2359 persons with RA aged 20–80 who were free of dental diseases between 2001 and 2010 were retrospectively enrolled from nationwide register-based data. They were then classified into HMs and non-HMs groups based on whether they ever used combined HMs after RA onset. Incidence rate and hazard ratios (HRs) of dental diseases were estimated for both groups by the end of 2013 via fitting Cox proportional hazards model. Results: Incidence rate of dental disease was reported to be lower in the HMs group than in the non-HMs group (90.21 per 1000 person-years versus 106.94 per 1000 person-years, respectively). RA individuals treated with HMs showed a significantly lower risk of dental diseases, especially dental caries, pulpitis, periodontitis, and stomatitis. Among commonly prescribed formulas, eleven herbal products significantly associated with a lower risk of dental diseases, such as Hai-Piao-Xiao, Yan-Hu-Suo, Chuan-Niu-Xi, Mo-Yao, Olibanum, Bei-Mu, Mu-Gua, Gui-Zhi-Shao-Yao-Zhi-Mu-Tang, Shao-Yao-Gan-Cao-Tang, Xue-Fu-Zhu-Yu-Tang, and Ping-Wei-San. Conclusions: The addition of HMs treatment may have advantages to proactively prevent sequent risk of dental disorders for persons with rheumatic diseases. A deeper exploration focusing on pharmacological action is needed to provide more reliable evidence for the improvement of susceptible individuals’ oral hygiene. Full article

The development of geopolymers as sustainable alternative binders has been accelerated by the environmental requirement to reduce the carbon footprint of cement. However, predicting their key properties, such as compressive strength, from their complex chemical composition remains a significant challenge. Although mixture ratios prepared on a macro-scale are widely used for quality control purposes, they do not account for the chemical structure, despite this having a direct impact on the materials’ structural properties. Predicting fundamental properties such as compressive strength from complex chemical compositions remains a significant challenge due to the nonlinear relationships between the elemental components. This research paper introduces a tailored hybrid machine learning framework that combines K-means clustering with classification algorithms. The method uses energy-dispersive X-ray spectroscopy (EDS) data to classify geopolymer samples into their specific mixture numbers, which allows scientists to predict material properties through compositional analysis. A new dataset featuring the elemental compositions of Si, Al, Na, Ca, O, and C, as well as the critical ratios of Si/Al and Ca/Si, was analyzed. The initial step involved clustering the data to discover natural compositional clusters, which served as the basis for training and testing five different classifiers, which included Random Forest (RF), Artificial Neural Networks (ANN), LightGBM, Naive Bayes (NB), and Linear Discriminant Analysis (LDA). The consequences proved that the hybrid method worked with outstanding efficiency. RF achieved the highest performance results through its 98% accuracy, 96% recall, 94% precision, and 95% F1-score results when it classified samples according to their clustered groups. SHAP (SHapley Additive exPlanations) and permutation feature importance analyses both showed that Si/Al proportion functioned as the most crucial predictive variable, while oxygen (O) content and silicon (Si) content followed in importance. The K-means cluster labels produced high accuracy results because they demonstrated that compositional data had strong natural groups, which matched the target property. The system delivers an efficient method which enables fast and dependable geopolymer property forecasts through direct analysis of chemical composition with chemical composition analysis, thus delivering essential information to enhance mix design processes and boost sustainable building material production. Full article

Submarine volcanic-hosted iron oxide deposits are critical archives for reconstructing the interplay between hydrothermal activities and marine redox conditions, yet the genesis of these deposits remains controversial. Here, we present a comprehensive geochronological and geochemical study on the Shikebutai iron deposit in the Western Tianshan, northwestern China, to constrain the mineralization age, the source of iron, and deposit genesis. The stratiform-to-lenticular orebodies are hosted within the Late Carboniferous marine volcanic–sedimentary sequence of the Yishijilike Formation. The iron ores consist primarily of hematite and quartz, with minor siderite and barite, exhibiting massive to locally banded textures. SHRIMP zircon U-Pb dating of the overlying andesite yields an age of 315.8 ± 1.5 Ma, consistent with the Sm–Nd isochron age of the iron ore samples (319 ± 26 Ma), precisely constraining the mineralization age to the Late Carboniferous (ca. 315–320 Ma). The geochemical compositions of the iron ore samples indicate negligible syn-depositional detrital contamination, as evidenced by low Al₂O₃ (<1.00 wt%) and TiO₂ (<0.20 wt%) contents. Low abundances of trace elements, including Sr (0.33–31.18 ppm), Hf (0.05–1.77 ppm) and Rb (1.49–39.02 ppm), further support the minimal detrital influence. Geochemical signatures, such as pronounced positive Eu anomalies (Eu/Eu = 1.62–7.12, mean 4.14), LREE enrichment ((La/Yb) _(PAAS) = 0.58–4.78), and near-chondritic Y/Ho ratios (mean 28.5), suggest a significant high-temperature (>250 °C) hydrothermal contribution. Moreover, the ε_Nd(t) values of iron ore samples (+1.99 to +2.93) are comparable to those of coeval andesites (+2.75 to +3.44) but exceed those of associated metasiltstones (+0.41 to +0.95), suggesting that ore-forming materials were derived from hydrothermal fluids leaching juvenile crust. The Shikebutai iron deposit exhibits geochemical and mineralogical similarities to modern Red Sea and East Pacific Rise metalliferous sediments, establishing the deposit as a product of active vent-proximal hydrothermal systems rather than marine chemical sediments such as banded iron formations. Full article

Glazes primarily utilize raw minerals like kaolinite. However, considering sustainable development, employing industrial solid waste offers greener design solutions and high economic efficiency. This study employs multiple analytical methods, including XRF, XRD, and SEM, to investigate the feasibility of replacing traditional glaze materials entirely with solid waste. It elucidates the mechanisms underlying changes in texture and color resulting from alterations in microstructure and chemical composition. Research on five different ratios of ceramic glaze composed of fly ash, blast furnace slag, silica fume, coal gangue, and desulfurization gypsum reveals that the implementation of solid waste-based glazes is feasible. The glazes formed a SiO₂–Al₂O₃–CaO system surface, all exhibiting anorthite and diopside as the primary crystalline forms. The results are as follows: 1. The content of Ca and Mg depends on the overall proportion of elements, with a Ca threshold of approximately 28%. Below this threshold, characteristics such as surface roughness and porosity are observed. Above this threshold, as seen in G3 and G4, crystal distribution becomes more dense. 2. Si is the key factor controlling crystal variation. Sample G5 exhibits good crystal continuity. Visually, its color appears distinctly deep red. 3. Samples G1 and G2 both contain approximately 4.8 wt% Fe₂O₃, but G2 exhibits more crystalline precipitation. Visually, G2 appears more reddish-yellow than G1. Higher crystallinity yields superior coloration. Full article

In the era of increasing generation of various waste streams, the possibility of utilizing them as secondary resources is of utmost importance and fully corresponds to the goals of the circular economy. Industrial residues from the pulp and paper industry, such as biomass combustion ash (FARP) and sludge from industrial wastewater treatment (PPWS), together with natural zeolite as a modifying additive, represent valuable sources enabling their integrated valorization. The present study aims to investigate the potential for their reuse through the development of sustainable material blends. A comprehensive analysis of the chemical composition and morphology of the obtained mixtures was carried out using inductively coupled plasma optical emission spectroscopy (ICP-OES), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The results indicate a tendency for the formation of mineral matrices dominated by calcium–sulfur–oxygen (Ca–S–O) phases, with the presence of calcium sulfate and aluminosilicate structures. The blends are associated with the formation of stable crystalline structures exhibiting potential pozzolanic activity. In this way, carbon is captured and fixed in a stable mineral form. The obtained results suggest the potential of these blends for use in low-carbon systems focused on waste valorization and carbon retention. The materials may be suitable for applications in construction, soil remediation, and environmental technologies, contributing to closing the resource loop “from farm to table and back again”. Full article

This study aimed to evaluate how hydration temperature, rotational speed, and screw restriction influence the extraction efficiency, physicochemical characteristics, and monosaccharide composition of chia seed mucilage (CSM). Optimal extraction conditions (43.7 Hz, 100% screw restriction and 50 °C) yielded an extraction efficiency of 65.69% and a mucilage yield of 7.66%, producing a material with an average particle size of 15.28 μm, a ζ-potential of 9.7 mV, and weak-gel rheological behavior. Structural analyses confirmed the absence of insoluble fiber and revealed crystalline phases including MgO, Ca₅P₈, K₂S, K₄P₆, and CaCO₃, along with typical polysaccharide functional groups (–OH, –CH, C=O, COO⁻, C–O). Moderate hydration temperature combined with controlled mechanical conditions favored the release of mucilage enriched in xylose, glucose, and arabinose, which are characteristic of seed coat polysaccharides. In contrast, minimal mechanical action or excessive seed disruption shifted the monosaccharide profile toward cell wall structural carbohydrates, indicating reduced mucilage purity. Elevated hydration temperature (75 °C) enhanced the solubilization of uronic acids and arabinose, suggesting increased extraction of acidic polysaccharide fractions associated with the seed coat matrix. These findings demonstrate that extraction parameters strongly determine CSM composition, structural integrity, and functional attributes. The results provide a basis for tailoring chia-derived polysaccharides for applications in hydrocolloid systems, bio-based materials, and functional polymer formulations. Full article

Based on the acid-sensitive characteristics of SBA-15 during synthesis, this study varied the acid types, pH values, and mixed acid ratios during SBA-15 preparation to enhance the performance of CaO/Cr-SBA-15 dual-functional materials (DFMs) in integrated CO₂ capture and utilization for oxidative dehydrogenation of ethane (ICCU-ODHE). It was found that the SBA-15 support synthesized in an H₂SO₄ environment exhibited a high specific surface area and abundant surface silanol groups, which facilitated the dispersion of Cr and increased the proportion of Cr⁶⁺ active sites, thereby achieving the highest ethane conversion. In contrast, the moderate surface acidity of the HCl-prepared support facilitated the selective dehydrogenation of ethane over Cr active sites, effectively inhibiting side reactions and maximizing ethylene selectivity. Further investigations into the effects of pH and mixed acids revealed that pH 1 is optimal for SBA-15 preparation. At this value, the support reached its maximum mesoporous ordering and specific surface area, allowing for optimal Cr dispersion. Consequently, the ethane conversion, ethylene selectivity, and DFM yield all reached their peak values. Any deviation from this pH led to degradation of the support structure and reduced Cr dispersion, resulting in a significant decline in catalytic performance. Among the tested materials, the CaO/Cr-SBA-15-Cl-S DFM synthesized with an HCl-H₂SO₄ mixed acid demonstrated the superior reactivity, achieving an ethylene yield of 33.95%. Long-term cycling tests indicated that the material possesses good stability, with its performance attenuation primarily attributed to coking and adsorbent sintering. Full article

Gypsum-based fire protection relies on thermally activated dehydration, where chemically bound water is released and evaporated, thereby providing an endothermic heat sink that delays heat penetration through assemblies. In parallel, inorganic hydrated salts are increasingly used as flame-retardant additives in gypsum-based systems to enhance heat absorption over specific temperature ranges. Fire simulation tools and performance-based fire engineering approaches require reliable kinetic data and reaction enthalpies that can be implemented as coupled thermal–chemical source terms. However, additive-specific kinetic datasets remain limited, particularly under restricted vapor exchange conditions representative of porous construction materials. This work investigates the thermal decomposition behavior and dehydration kinetics of Aluminum Trihydrate (Al(OH)₃, ATH), Magnesium Hydroxide (Mg(OH)₂, MDH), Calcium Aluminate Sulfate (3CaO·Al₂O₃·3CaSO₄·32H₂O, CAS), and Magnesium Sulfate Heptahydrate (MgSO₄·7H₂O, ESM) with emphasis on vapor-restricted conditions representative of confined porous systems. Differential scanning calorimetry (DSC) experiments were conducted at three heating rates (2, 10, and 20 K/min for MDH, CAS and ESM and 20, 40 and 60 K/min for GB-ATH) up to 600 °C using pinhole crucibles to simulate autogenous vapor pressure. The thermal analysis indicates that ATH and MDH exhibit predominantly single-step dehydration behavior, while ESM shows a complex multi-step mechanism. Although CAS presents a single dominant thermal peak in the DSC signal, the isoconversional analysis reveals a multi-stage reaction behavior, demonstrating that peak-based interpretation alone may be insufficient for such systems. Kinetic parameters were determined using both model-free (Starink) and model-fitting approaches in accordance with the recommendations of the Kinetics Committee of the International Confederation for Thermal Analysis and Calorimetry (ICTAC). All reactions were consistently described using the Avrami–Erofeev model as an effective phenomenological representation of the conversion behavior. The extracted kinetic triplets were validated through numerical simulations, showing good agreement with experimental conversion and reaction rate data. The resulting kinetic parameters and dehydration enthalpies provide a physically consistent dataset for the description of dehydration processes under restricted vapor exchange. These results support the development of thermochemical models for gypsum-based systems; however, their transferability to full-scale assemblies remains subject to validation under coupled heat- and mass-transfer conditions. Full article