Search Results (30)

The global environmental challenges of solid waste accumulation and aquatic eutrophication demand innovative and sustainable strategies. This study introduces a circular “waste-treats-waste” approach by converting dolomite-rich phosphate tailings (PT), a widespread industrial by-product, into a high-value adsorbent for phosphorus (P) removal. Thermal modification at 950 °C for 1 h dramatically enhanced the adsorption capacity by approximately 45 times, from 2.52 mg/g (raw PT) to 112.41 mg/g. This performance is highly competitive with, and often superior to, many engineered adsorbents. The calcination process was pivotal, decomposing carbonates into highly active CaO and MgO while developing a porous structure. Using a multi-technique characterization approach (X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), TESCAN VEGA3 tungsten filament scanning electron microscope (SEM), the Brunauer–Emmett–Teller method (BET)), the key immobilization mechanism was identified as hydroxyapatite formation, driven by Ca²⁺/Mg²⁺-phosphate precipitation and surface complexation. Nonlinear regression analysis revealed that the adsorption kinetics obeyed the pseudo-second-order model, and the equilibrium data were best described by the Freundlich isotherm. This indicates a chemisorption process occurring on a heterogeneous surface, consistent with the complex structure created by thermal modification. Notably, post-adsorption pore structure expansion suggested synergistic pore-filling and surface reorganization. This work not only demonstrates a circular economy paradigm for repurposing industrial solid waste on a global scale but also offers a cost-effective and high-performance pathway for controlling phosphorus pollution in aquatic systems, contributing directly to resource efficiency and sustainable environmental remediation. Full article

Bentonite is the most widely used raw material for producing organoclays, which have numerous industrial and environmental applications. Due to their hydrophobicity, high swelling, and strong affinity for organic compounds, organoclays are effective in removing organic solvents from contaminated water originating from pipeline leaks, oil spills, traffic accidents, and industrial discharges. Such contamination not only degrades water quality but also forms surface films that hinder oxygen transfer, threatening aquatic ecosystems. In this study, two sodium bentonites with different specific surface areas (30 and 50 m²/g) were modified with three quaternary ammonium salts of varying molar masses and alkyl chain lengths (Sun, Arq, and Arm) to evaluate their performance in organic solvent sorption (gasoline, diesel, and kerosene). The materials were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential thermal analysis (DTA), scanning electron microscopy (SEM), and swelling capacity and sorption efficiency. The swelling capacity was determined according to ASTM D5890-19 (Foster method) using gasoline, diesel, kerosene, toluene, and xylene, while the sorption efficiency was assessed following ASTM F726-17 in gasoline, diesel, and kerosene, chosen due to their high potential for water contamination and frequent occurrence in oil spill and leakage scenarios. These solvents also differ in polarity and aromatic content, providing a relevant model for hydrocarbon mixtures commonly found in the environment. Results showed that the interaction between the clay and the surfactant depended strongly on the modifier’s chemical structure. The sorption capacity increased with greater interlayer expansion, surfactant molar mass, and specific surface area of the clay. Among all samples, the Arm-modified natural bentonite (VLArm) exhibited the best performance, with adsorption capacities of up to 6 g/g for diesel, 5 g/g for gasoline, and 5 g/g for kerosene. These values exceeded most previously reported organoclays. These findings demonstrate that optimizing the combination of clay properties and surfactant chemistry can yield highly efficient, low-cost organoclays for environmental remediation of organic contaminants. Full article

The development of highly efficient and stable non-noble metal catalysts for volatile organic compound (VOCs) abatement remains a pressing challenge. Mn-based perovskites exhibit superior thermal stability as redox catalysts but suffer from limited activity in light alkane combustion. This study systematically investigates the performance of SmMnO₃ (SMO) perovskite catalysts for propane oxidation through selective etching of Sm species. By precisely controlling the etching process, the removal of surface Sm exposes more active sites and significantly increases the specific surface area from 22.05 m²·g⁻¹ for pristine SMO to 66.15 m²·g⁻¹. SEM and N₂ adsorption–desorption analysis revealed that prolonged etching induces surface roughening and pore channel expansion. XPS and XANES measurements confirmed that an increased Mn⁴⁺/Mn³⁺ ratio enhances reactant adsorption and accessibility to active sites. The etched catalysts exhibited markedly improved activity for propane oxidation, achieving a ~50 °C reduction in light-off temperature compared to the raw SMO. This performance enhancement is attributed to the synergistic effects of enhanced oxygen mobility, elevated Mn⁴⁺ content, and abundant oxygen vacancies. Further characterization via Raman spectroscopy and H₂-TPR revealed weakened Jahn–Teller distortion and lower reduction temperatures, reflecting optimized Mn–O interactions and superior redox properties. Among the samples, SMO-20 demonstrated exceptional stability. Moreover, the SMO-20/cordierite monolithic catalyst maintained outstanding catalytic performance over 1000 h of operation. This work offers a facile and effective approach to engineer perovskite catalysts and provides new insights into structure–activity relationships in VOC oxidation. Full article

With the expansion of industrial production capacity, a substantial volume of hazardous wastewater containing Pb (II) and Ni (II) requires treatment. Kaolin, a low-cost adsorbent with strong adsorption properties, was modified through thermal activation at 750 °C, 850 °C, and 950 °C to enhance its adsorption capacity. Following the optimization of pH, reaction time, temperature, heavy metal concentrations, and adsorbent amount, the 850-K was found to have the best removal efficiency, achieving removal rates > 90% for both PbCl₂ and NiCl₂, and the removal efficiency of PbCl₂ was higher compared to NiCl₂. The pseudo-second-order kinetics and Langmuir model could reasonably match the adsorption processes of PbCl₂/NiCl₂. The experimental findings were corroborated through simulations of adsorption distance, variations in bond length/bond angle, adsorption energy, frontier molecular orbital, charge density, and differential charge density. The differences in reactions between adsorbents and PbCl₂/NiCl₂ were primarily due to the electron transfer direction and bonding mechanisms. The O atoms were the main reactive atoms of the adsorbents, capable of forming covalent bonds with both PbCl₂ and NiCl₂, and the Cl atoms could form either ionic or covalent bonds with the adsorbent. Pb could form covalent bonds with the adsorbent, while Ni might be adsorbed through electrostatic interactions. Full article

Mine effluents represent a serious environmental problem on a global scale. Therefore, the effective treatment of this water is a serious issue in the scientific field. The adsorption process seems to be one of the attractive methods, especially due to the simplicity of design, affordability or high efficiency. The latest scientific knowledge has shown that the use of waste and natural adsorbents is economical and effective. This study aimed to evaluate the efficiency of the adsorption process of natural and waste materials—zeolite, bentonite and fly ash—under the influence of temperature and modification of these adsorbents. The novelty of this study resides in an adjustment of the modification method of adsorbents compared to previous research: thermal–alkaline treatment versus hydrothermal one. Another novelty is the use of modified fly ash from biomass combustion as an adsorbent in comparison with the previously used fly ash from coal combustion. The modification of the adsorbents made the adsorption process more effective at all experimental concentrations. The characterisation of adsorbent samples was performed using X-ray diffraction (XRD). The parameters of the adsorption isotherms, Langmuir, Freundlich and Temkin, were estimated by nonlinear regression analysis. The adsorption capacity of Cu(II) of fly ash was comparable to natural adsorbents. Adsorption processes were better described by pseudo-second-order kinetics. At the end of this study, the suitability of using the adsorbents to reduce the concentration of Cu(II) in neutral mine effluents was observed in the following order at 30 °C: unmodified fly ash > modified bentonite > unmodified zeolite. At the temperatures of 20 °C and 10 °C, the same trend of the suitability of adsorbents use was confirmed: modified bentonite > modified zeolite > modified fly ash. The practical applicability of this study lies in the expansion of knowledge in the field of adsorption processes and in the improvement of waste management efficiency of heating plants not only in Slovakia, but also globally. Full article

The commercialization of proton-conducting fuel cells (PCFCs) is hindered by the limited electroactivity and durability of cathodes at intermediate temperatures ranging from 400 to 700 °C, a challenge exacerbated by an insufficient understanding of high-entropy perovskite (HEP) materials for oxygen reduction reaction (ORR) optimization. This study introduces an yttrium-doped HEP to address these limitations. A comparative analysis of Ce_0.2−xY_xBa_0.2Sr_0.2La_0.2Ca_0.2CoO_3−δ (x = 0, 0.2; designated as CBSLCC and YBSLCC) revealed that yttrium doping enhanced the ORR activity, reduced the thermal expansion coefficient (19.9 × 10⁻⁶ K⁻¹, 30–900 °C), and improved the thermomechanical compatibility with the BaZr_0.1Ce_0.7Y_0.1Yb_0.1O_3−δ electrolytes. Electrochemical testing demonstrated a peak power density equal to 586 mW cm⁻² at 700 °C, with a polarization resistance equaling 0.3 Ω cm². Yttrium-induced lattice distortion promotes proton adsorption while suppressing detrimental Co spin-state transitions. These findings advance the development of durable, high-efficiency PCFC cathodes, offering immediate applications in clean energy systems, particularly for distributed power generation. Full article

In the production process of horizontal wells, wellbore temperature data play a critical role in predicting shale gas production. This study proposes a coupled thermo-hydro-mechanical (THM) mathematical model that accounts for the influence of the stress field when determining the distribution of wellbore temperature. The model integrates the effects of heat transfer in the temperature field, gas transport in the seepage field, and the mechanical deformation of shale induced by the stress field. The coupled model is solved using the finite difference method. The model was validated against field data from shale gas production, and sensitivity analyses were conducted on seven key parameters related to the stress field. The findings indicate that the stress field exerts an influence on both the wellbore temperature distribution and the total gas production. Neglecting the stress field effects may lead to an overestimation of shale gas production by up to 12.9%. Further analysis reveals that reservoir porosity and Langmuir volume are positively correlated with wellbore temperature, while permeability, Young’s modulus, Langmuir pressure, the coefficient of thermal expansion, and adsorption strain are negatively correlated with wellbore temperature. Full article

Traditional β-eucryptite (LiAlSiO₄) is renowned for its unique characteristics of low thermal expansion and high temperature thermal stability, making it an ideal material for precision instruments and aerospace applications. In this study, β-eucryptite was fabricated into an aerogel structure through the sol–gel process and supercritical drying method and using alumina sol as a cost-effective precursor. The synthesized β-eucryptite aerogel demonstrated unique properties including a negative thermal expansion coefficient (−7.85 × 10⁻⁶ K⁻¹), low density (0.60 g/cm³), and high specific surface area (18.1 m²/g). X-ray diffraction (XRD) and transmission electron microscopy (TEM) mutually corroborated the crystalline structure of β-eucryptite, with XRD confirming the phase purity and TEM imaging revealing well-defined crystal lattice characteristics. Combined nitrogen adsorption–desorption analysis and scanning electron microscopy observations supported the hierarchical porous microstructure, with SEM visualizing interconnected nanoporous networks and nitrogen sorption data verifying the porosity. The negative thermal expansion behavior was directly linked to the β-eucryptite crystal structure, as collectively validated by thermal expansion measurements. Additionally, Fourier transform infrared spectroscopy (FTIR) independently confirmed the aluminosilicate framework structure through characteristic vibrational modes. This research shows the innovation in the synthesis of β-eucryptite aerogel, especially its application potential in precision instruments and building materials that need low thermal expansion and high stability, and the use of aluminum sol as an aluminum source has simplified the preparation steps and reduced production costs. Full article

Uniform acid distribution is a critical challenge and a key factor for the successful acidizing of carbonate reservoirs. Previous experimental studies have shown that nanoparticles can enhance the viscosity and thermal resistance of viscoelastic surfactant (VES) fracturing fluids. However, there has been limited research on the effects of nanoparticles on the wormhole propagation and diversion performance of VES acid. This paper establishes a nanoparticle VES acid rheological model based on rheology experiments, and introduces a porous medium temperature field and nanoparticle adsorption model into a two-scale continuum model to establish a mathematical model for the expansion of wormholes in nanoparticle VES acid. The accuracy of the wormhole model is verified through laboratory experiments. The effects of permeability contrast, initial acid temperature, and nanoparticle adsorption on the diversion performance and wormhole propagation of nanoparticle VES acid are analyzed. The results indicate that nanoparticle VES acid differs from conventional VES acid, with its invaded zone divided into high-viscosity and low-viscosity zones. The presence of the high-viscosity zone allows nanoparticle VES acid to improve wormhole propagation in low-permeability cores by 16.2% compared to conventional VES acid. At 393 K, nanoparticle VES acid has a better diversion effect in carbonate cores with permeability contrast of 10, as the acid fluid flows faster in high-permeability cores, resulting in wormhole shapes with more branches. Numerical model results show that when the permeability contrast is 8, increasing the injection temperature of the acid solution from 293 K to 368 K improves the ability of low-permeability cores by 33.3%. This study establishes a mathematical model for nanoparticle VES acid based on laboratory experiments and numerical simulations, investigates the effects of nanoparticles on VES rheological properties under acidic conditions, and clarifies the wormhole propagation and acid diversion behavior of nanoparticle VES acid, providing guidance for future field applications of this acid. Full article

Meringue has limited the use of meringue for personalization because of its thermally unstable system. Citric acid (CA) enhancement of egg white protein (EWP) foaming properties is proposed for the preparation of 3D-printed meringues. The results showed that CA increased the viscosity, exposure of hydrophobic groups (79.8% increase), and free sulfhydryl content (from 5 µmol/g to 34.8 µmol/g) of the EWP, thereby increasing the foaminess (from 50% to 178.2%). CA treatment increased the rates of adsorption, stretching, and orientation of EWP at the air–water interface to form multiple layers, resulting in a delay in foam thinning. The secondary structure of CA-treated EWP remained intact, and the exposure of amino acid residues in the tertiary structure increased with the expansion of the hydrophobic region. CA-treated EWP-prepared protein creams had a suitable viscosity (from 233.4 Pa·s to 1007 Pa·s at 0.1 s⁻¹), shear thinning, structural restorability, and elasticity, which ensured good fidelity of their printed samples. Experiments involving 3D printing of CA-treated EWP showed that CA could significantly enhance the 3D printing fidelity of EWP. Our study could provide new ideas for the development of customizable 3D-printed foam food products. Full article

In this study, a new polyionic polymer inhibitor, TIL-NH₂, was developed to address the instability of shale gas horizontal wells caused by water-based drilling fluids. The structural characteristics and inhibition effects of TIL-NH₂ on mud shale were comprehensively analyzed using infrared spectroscopy, NMR spectroscopy, contact angle measurements, particle size distribution, zeta potential, X-ray diffraction, thermogravimetric analysis, and scanning electron microscopy. The results demonstrated that TIL-NH₂ significantly enhances the thermal stability of shale, with a decomposition temperature exceeding 300 °C, indicating excellent high-temperature resistance. At a concentration of 0.9%, TIL-NH₂ increased the median particle size of shale powder from 5.2871 μm to over 320 μm, effectively inhibiting hydration expansion and dispersion. The zeta potential measurements showed a reduction in the absolute value of illite’s zeta potential from −38.2 mV to 22.1 mV at 0.6% concentration, highlighting a significant decrease in surface charge density. Infrared spectroscopy and X-ray diffraction confirmed the formation of a close adsorption layer between TIL-NH₂ and the illite surface through electrostatic and hydrogen bonding, which reduced the weakly bound water content to 0.0951% and maintained layer spacing of 1.032 nm and 1.354 nm in dry and wet states, respectively. Thermogravimetric analysis indicated a marked reduction in heat loss, particularly in the strongly bound water content. Scanning electron microscopy revealed that shale powder treated with TIL-NH₂ exhibited an irregular bulk shape with strong inter-particle bonding and low hydration degree. These findings suggest that TIL-NH₂ effectively inhibits hydration swelling and dispersion of shale through the synergistic effects of cationic imidazole rings and primary amine groups, offering excellent temperature and salt resistance. This provides a technical foundation for the low-cost and efficient extraction of shale gas in horizontal wells. Full article

Poly(propylene carbonate-co-phthalate) (PPC-P) is an amorphous copolymer of aliphatic polycarbonate and aromatic polyester; it possesses good biodegradability, superior mechanical performances, high thermal properties, and excellent affinity with CO₂. Hence, we fabricate PPC-P foams in an autoclave by using subcritical CO₂ as a physical blowing agent. Both saturation pressure and foaming temperature affect the foaming behaviors of PPC-P, including CO₂ adsorption and desorption performance, foaming ratio, cell size, porosity, cell density, and nucleation density, which are investigated in this research. Moreover, the low-cost PPC-P/nano-CaCO₃ and PPC-P/starch composites are prepared and foamed using the same procedure. The obtained PPC-P-based foams show ultra-high expansion ratio and refined microcellular structures simultaneously. Besides, nano-CaCO₃ can effectively improve PPC-P’s rheological properties and foamability. In addition, the introduction of starch into PPC-P can lead to a large number of open cells. Beyond all doubt, this work can certainly provide both a kind of new biodegradable PPC-P-based foam materials and an economic methodology to make biodegradable plastic foams. These foams are potentially applicable in the packaging, transportation, and food industry. Full article

The adsorption of CO₂ fracturing fluid into coal reservoirs causes the expansion of the coal matrix volume, resulting in changes in the fracture opening, which alters the permeability of the coal reservoir. However, it is not yet clear whether thermal expansion during CO₂ adsorption on coal is the main cause of coal adsorption expansion. Therefore, by testing the thermal properties, expansion coefficient, and adsorption heat of the three coal samples, the adsorption thermal expansion characteristics of coal and their impact on the permeability of coal reservoirs are clarified. The results reveal the following: (1) Under the same conditions, the adsorption heat increases with increasing pressure, while it decreases with increasing temperature. The relationship between adsorption heat and pressure conforms to the Langmuir equation before 40 °C, and it follows a second-order equation beyond 40 °C. At 100 °C, the adsorption heat of coal samples to CO₂ is primarily determined by temperature. (2) The maximum temperature variation in coal samples from Xinjiang, Liulin, and Zhaozhuang during CO₂ adsorption is 95.767 °C, 87.463 °C, and 97.8 °C, respectively. The maximum thermal expansion rates are 12.66%, 5.74%, and 14.37%, and the maximum permeability loss rates are 16.16%, 7.51%, and 18.24%, respectively, indicating that thermal expansion is the main reason for coal adsorption expansion. (3) This research can elucidate the impact of CO₂ fracturing fluid on coal reservoirs and its potential application value, thus providing theoretical support for coalbed methane development and CO₂ geological storage. Full article

With the purpose of obtaining synthetic materials from other natural sources for industrial and technological applications, a thermal alteration study was carried out with commercial vermiculites of different purity and origin. For this objective, samples were subjected to 1000 °C in a furnace both at ambient and reduced (N₂/Ar) atmospheres. The thermal behavior and physicochemical properties of the different vermiculites were investigated by X-ray diffraction (XRD), thermal analysis (TG and DTG), and scanning electron microscopy (SEM), and their textural parameters were analyzed by BET treatment. The transformations undergone by the investigated commercial vermiculites subjected to heating treatments caused textural and structural changes in them. There was a decrease in the specific surface area, adsorption capacity, and pore volume values for the samples treated with in situ heating at 1000 °C, both at ambient and reduced atmospheres, and the samples were treated with ex situ abrupt heating at 1000 °C at ambient conditions. There was a decrease in the specific surface area, adsorption capacity, and pore volume values for the samples treated with in situ heating at 1000 °C, both in ambient and reduced atmospheres, which was not observed in the samples treated with an ex situ abrupt heating at 1000 °C at ambient conditions. This corroborated with our findings that the expansion in the first type of thermal treatment produced less separation of the exfoliation sheets than the expansion in the second type of thermal treatment. These textural changes, together with the structural ones, could play a fundamental role in the choice of industrial and technological applications for which these materials could be used. Full article

Lithium–sulfur (Li–S) batteries have received extensive attention due to their numerous advantages, including a high theoretical specific capacity, high energy density, abundant reserves of sulfur in cathode materials, and low cost. Li–S batteries also face several challenges, such as the insulating properties of sulfur, volume expansion during charging and discharging processes, polysulfide shuttling, and lithium dendritic crystal growth. In this study, a composite of a porous multi-site diatomite-loaded graphene oxide material and a PAN fiber membrane is developed to obtain a porous and high-temperature-resistant GO/diatomite/polyacrylonitrile functional separator (GO/DE/PAN) to improve the electrochemical performance of Li–S batteries. The results show that the use of GO/DE/PAN helps to inhibit lithium phosphorus sulfide (LPS) shuttling and improve the electrolyte wetting of the separator as well as the thermal stability of the battery. The initial discharge capacity of the battery using GO/DE/PAN is up to 964.7 mAh g⁻¹ at 0.2 C, and after 100 cycles, the reversible capacity is 683 mAh g⁻¹ with a coulombic efficiency of 98.8%. The improved electrochemical performance may be attributed to the porous structure of diatomite and the layered composite of graphene oxide, which can combine physical adsorption and spatial site resistance as well as chemical repulsion to inhibit the shuttle effect of LPS. The results show that GO/DE/PAN has great potential for application in Li–S batteries to improve their electrochemical performance. Full article