Search Results (417)

The controlled incorporation of halogens into carbon materials remains a challenge, particularly under mild and scalable conditions. In this work, we investigate the fixation of iodine on high-surface-area graphite (HSAG-100) using green solvents and moderate temperatures. Commercial HSAG was treated with iodine in aqueous and in organic media, with and without promoters, and characterized by XPS, LEIS, N₂ physisorption, TGA/TPD, and XRD. The results reveal that iodine contents up to ~0.6 at% can be achieved, with incorporation strongly influenced by solvent and reaction time. XPS and LEIS confirmed the presence of C–I bonds, while BET analysis showed only moderate decreases in surface area and unchanged mesopore size distribution. Thermogravimetric and TPD analyses demonstrated the high thermal stability of C–I species, and XRD patterns ruled out intercalation between graphene layers. Collectively, these findings demonstrate that iodine can be covalently anchored to HSAG under mild conditions, preserving the graphitic structure and generating stable edge functionalities, thus opening a route for the design of halogen-doped carbons for catalytic and electrochemical applications. Full article

Among the many nanomaterials studied for biomedical uses, silica and gold nanoparticles have gained significant attention because of their unique physical and chemical properties and their compatibility with living tissues. Mesoporous silica nanoparticles (MSNs) have great stability and a large surface area, while gold nanoparticles (AuNPs) display remarkable optical features. Both types of nanoparticles have been widely researched for their individual roles in drug delivery, imaging, biosensing, and therapy. When combined with gadolinium (Gd), a common contrast agent, these nanostructures provide improved imaging due to gadolinium’s strong paramagnetic properties. This study focuses on incorporating gold nanoparticles and gadolinium into a silica matrix to develop a theranostic system. Various analytical techniques were used to characterize the nanocomposites, including infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-Vis), thermogravimetric analysis (TGA), nitrogen adsorption, scanning electron microscopy (SEM), dynamic light scattering (DLS), X-ray fluorescence (XRF), X-ray diffraction (XRD), vibrating sample magnetometry (VSM), and neutron activation analysis (NAA). Techniques like XRF mapping, XANES, nitrogen adsorption, SEM, and VSM were crucial in confirming the presence of gadolinium and gold within the silica network. VSM and EPR analyses confirmed the attenuation of the saturation magnetization for all nanocomposites. This validates their potential for biomedical applications in diagnostics. Moreover, activating gold nanoparticles in a nuclear reactor generated a promising radioisotope for cancer treatment. These results indicate the potential of using a theranostic nanoplatform that employs mesoporous silica as a carrier, gold nanoparticles for radioisotopes, and gadolinium for imaging purposes. Full article

This work employed peach stones as the precursor material for producing activated carbon (AC-PS). AC-PS was impregnated with H₃PO₄ and carbonized using a pyrolysis reactor under a reducing atmosphere. The surface area, average pore size, and total pore volume of AC-PS were determined using the BET method. Morphological characteristics of AC-PS were observed through scanning electron microscopy (SEM), the surface composition was identified by energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD) analyses were conducted to determine the crystalline structure of carbon. The thermal stability of AC-PS and its interactions with lead and cadmium were analyzed by thermogravimetric analyses (TGA/DTG) and infrared spectra (FTIR), respectively. The Elovich model described the adsorption kinetics of both lead and cadmium, and the Weber and Morris model indicated intraparticle diffusion as the controlling mechanism of the adsorption process. The equilibrium study showed that the Freundlich model was adequate for both ions, with adsorption capacities increasing with temperature, reaching around 150 mg g⁻¹ for lead and 80 mg g⁻¹ for cadmium at 45 °C. Economic analysis indicated costs of $0.25 g⁻¹ and $0.51 g⁻¹ for the removal of lead and cadmium from the contaminated water, respectively. Full article

The anthrone-based dummy molecularly imprinted membrane (DIM) was successfully synthesized using a semi-interpenetrating polymer network (semi-IPN) approach for the selective recognition and adsorption of fluorene and phenanthrene in aqueous systems. Fourier-transform infrared spectroscopy (FTIR) confirmed the successful incorporation of functional groups, while scanning electron microscopy (SEM) revealed a uniform porous morphology favorable for analyte diffusion. Thermogravimetric analysis (TGA) demonstrated good thermal stability, and Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda (BJH) analyses indicated an enhanced surface area and mesoporous structure that supported improved adsorption performance. Adsorption isotherm studies revealed favorable adsorption behavior, with the maximum adsorption capacities of the DIM calculated to be 130.857 mg/g for fluorene and 453.030 mg/g for phenanthrene. The imprinting factors (IFs) were approximately 2.01 for fluorene and 2.17 for phenanthrene, confirming the successful imprinting effect. The recovery values achieved were 86.61% for fluorene and 92.40% for phenanthrene, demonstrating the efficiency and selectivity of the fabricated membrane. These results highlight the potential application of the anthrone-based DIM in the environmental monitoring of polycyclic aromatic hydrocarbons (PAHs). Full article

This paper presents a detailed analysis of the thermal and flammability properties of polylactide- (PLA) and poly(ethylene terephthalate)- (PET) based polymer blends with biofillers, such as calcium lignosulfonate (CLS), lignosulfonamide (SA) and lignosulfonate modified with tannic acid (BMT) and gallic acid (BMG). Calorimetric studies revealed the presence of two glass transitions, one cold crystallization temperature, and two melting points, confirming the partial immiscibility of the PLA and PET phases. The additives had different effects on the temperatures and ranges of phase transformations—BMT restricted PLA chain mobility, while CLS acted as a nucleating agent that promoted crystallization. Thermogravimetric analyses (TGA) analyses showed that the additives significantly affected the thermal stability under oxidizing conditions, some (e.g., BMG) lowered the onset degradation temperature, while the others (BMT, SA) increased the residual char content. The additives also altered combustion behavior; particularly BMG that most effectively reduced flammability, promoted char formation, and extended combustion time. CLS reduced PET flammability more effectively than PLA, especially at higher PET content (e.g., 65% reduction in PET for 2:1/CLS). SA inhibited only PLA combustion, with strong effects at higher PLA content (up to 76% reduction for 2:1/SA). BMT mainly reduced PET flammability (48% reduction in 1:1/BMT), while BMG inhibited PET more strongly at lower PET content (76% reduction for 2:1/BMG). The effect of each additive also depended on the PLA:PET ratio in the blend. FTIR analysis of the char residues revealed functional groups associated with decomposition products of carboxylic acids and aromatic esters. Ultimately, only blends containing BMT and BMG met the requirements for flammability class FV-1, while SA met FV-2 classification. BMG was the most effective additive, offering enhanced thermal stability, ignition delay, and durable char formation, making it a promising bio- based flame retardant for sustainable polyester materials. Full article

Internal erosion is a significant issue caused by water flow within soils, resulting in structural collapse of hydraulic structures, particularly in coarse soils located near rivers. These soils typically exhibit granulometric instability due to low clay content, resulting in poor hydraulic and mechanical properties. To mitigate this problem, cement treatment is applied as an alternative to soil removal, reducing transportation and storage costs. The hole erosion test (HET) and Crumbs tests, shearing behaviour through consolidated undrained (CU) triaxial, and microstructure analyses regarding scanning electron microscopy (SEM), mercury intrusion porosimeter (MIP) and thermogravimetric analysis (TGA) were conducted for untreated and treated coarse soil specimens with varying cement contents (1%, 2%, and 3%) and curing durations (1, 7, and 28 days). The findings indicate a reduction in the loss of eroded particles and overall stability of treated soils, along with an improvement in mechanical properties. SEM observations reveal the development of hydration gel after treatment, which enhances cohesion within the soil matrix, corroborated by TGA analyses. MIP reveals the formation of a new class of pores, accompanied by a reduction in dry density. This study demonstrates that low cement addition can transform locally unsuitable soils into durable construction materials, reducing environmental impact and supporting sustainable development. Full article

In this study, we present a novel and straightforward approach for the synthesis of copolymers and nanocomposites based on α- and β-pinene, employing an eco-friendly and cost-effective nano-reinforcing filler. The copolymers (α-co-β-P) were produced through cationic copolymerization, using AlCl₃ as a catalyst. The structural characterization of the resulting copolymer was validated through FT-IR, ¹H-NMR spectroscopy, and differential scanning calorimetry (DSC). The molecular weight of the obtained polymer is determined by Gel Permeation Chromatography (GPC) analysis and is about 4500 g/mol. Nanocomposites (α-co-β-P/Clay 2, 5, 8, and 10% by weight of nano-clay) were synthesized by combining clay and α-co-β-P copolymer in solution using ultrasonic irradiation. This ultrasound-assisted method was employed to enhance and assess the structural, morphological, and thermal properties of the pure copolymer. The morphology of the resultant nanocomposites was characterized using infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Thermogravimetric analysis (TGA) revealed that the nanocomposites exhibit a higher degradation temperature compared to the pure copolymer. The analyses provided evidence of the chemical modification of nano-clay layers and their uniform dispersion in the α-co-β-P copolymer matrix. Exfoliated structures were achieved for lower clay concentration (2% by weight), while intercalated structures and immiscible regions were observed for higher clay concentrations (5, 8, and 10% by weight). The antioxidant activity of α-pinene, β-pinene, and the obtained nanocomposites were studied using DPPH (2,2-diphenyl-1-picrylhydrazyl) as a model free-radical. The results demonstrate a significant antioxidant potential of the nanocomposites, showcasing their ability to effectively neutralize free-radicals. Finally, a novel procedure was devised for the rapid synthesis of copolymers and nanocomposites using α- and β-pinene. Full article

The Dazhuzhuang, Biting, and Likou Sites are located along the Hui River basin in Yongcheng, eastern Henan. These three sites are situated close to each other and all yielded Longshan Culture period (2300–1800 BCE) remains, including large quantities of pottery with similar stylistic characteristics. However, archaeological surveys did not discover kiln sites at any of the three locations. To investigate the sources of Longshan period pottery in this region, its firing technology, and whether pottery circulated between the sites, this study employed a combination of X-ray fluorescence spectroscopy (XRF), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM) to conduct a comprehensive scientific analysis of pottery unearthed from Longshan Culture contexts at the Dazhuzhuang, Likou, and Biting Sites in the Huai River basin, Yongcheng, Henan Province. The results reveal significant differences among the sites in terms of raw material selection, chemical composition, and technological characteristics. Pottery from the Dazhuzhuang Site exhibits with diverse clay sources. The Likou Site is characterized by highly homogeneous compositions derived from relatively high-alumina, low-iron clays, indicating standardized production practices. In contrast, the Biting Site shows greater variability in raw materials and functional differentiation. Thermal and microstructural analyses indicate that the dense glassy phase of black pottery was achieved through reducing firing conditions. In contrast, gray pottery was manufactured with calcareous additives to produce a porous structure. Full article

The rubber industry is facing increasing pressure to adopt sustainable practices due to environmental concerns associated with the use of non-renewable resources and the growing accumulation of waste tyres and agricultural byproducts. This study explores the potential of partially replacing conventional carbon black (CB) with sustainable alternatives derived from agricultural waste (wine by-products) and pyrolysed waste tyres in natural rubber/styrene-butadiene rubber (NR/SBR) composites for tyre applications. A series of NR/SBR composites were formulated with varying ratios of CB to agricultural waste and pyrolysed tyre waste, while maintaining consistent levels of other additives. The resulting composites were then subjected to a comprehensive suite of analyses, including scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) surface area measurements, Fourier transform infrared spectroscopy (FTIR), bound rubber content determination, Payne effect analysis, thermogravimetric analysis (TGA), dynamic mechanical thermal analysis (DMTA), and mechanical property testing. Furthermore, a Life Cycle Assessment (LCA) and Life Cycle Costing (LCC) analysis were conducted to evaluate the environmental and economic viability of the proposed CB replacements. The results reveal that the incorporation of agricultural waste and pyrolysed tyre waste can significantly impact the curing behaviour, mechanical properties, and thermal stability of rubber composites. Importantly, some of the formulations demonstrate comparable tensile strength, elongation at break, and hardness compared to traditional CB-filled composites. The LCA and LCC analyses further highlight the potential for substantial reductions in greenhouse gas emissions, fossil resource depletion, and overall production costs, thereby supporting the transition toward more sustainable tyre manufacturing practices. Full article

The spontaneous combustion of sulfide ores (SOSC) is an extremely dangerous mining disaster that directly threatens safety production in mines and causes far-reaching negative impacts on the surrounding ecosystem. In this study, oxidation weight gain experiments, self-heating temperature and ignition temperature tests, and thermogravimetric analysis (TGA) were conducted to detect the spontaneous combustion characteristics of sulfide ores with different sulfur contents (40.29%, 34.56%, 24.81%, and 14.2%). The results show that the sulfur content significantly affects the spontaneous combustion characteristics of sulfide ores. As the sulfur content decreased, the oxidized weight gain rate decreased overall, and the self-heating temperature (135, 152.5, 162.5, and 176.9 °C) and ignition temperature (425.3, 438.6, 455.4, and >500 °C) increased. The three combustion stages of the SOSC were divided based on the TG and DTG curves: low-temperature oxidation stage, combustion decomposition stage, and slow burnout stage. Furthermore, KAS and FWO methods were used to obtain the apparent activation energy in the combustion decomposition stage. The apparent activation energy decreased significantly with the increase in the sulfur content. The results of all experiments and analyses showed that sulfide ores with high sulfur content have a stronger tendency to undergo spontaneous combustion. The research results have important theoretical and practical implications for the prevention of SOSC. Full article

Co-combustion is regarded as an effective means for high-efficiency utilization of low-quality fuels. However, low-quality fuel has problems such as low energy density and high water content. The fuel quality and blending performance can be further optimized by the pretreatment of low-quality fuel, for example, calorific value, hydrophobicity, and NO conversion rate. Based on the idea of co-upgradation, this study systematically investigates the effects of integrated upgrading on fuel quality and hydrophobicity under different conditions. In this study, lignite and wheat straw were selected as research objects. The co-upgrading experiments of wheat straw and lignite were conducted at reaction temperatures of 170 °C, 220 °C, and 270 °C in flue gas and air atmospheres with biomass blending ratios of 0%, 25%, 50%, 75%, and 100%. SEM (scanning electron microscopy) and nitrogen (N₂) adsorption analyses showed that under low-temperature and low-oxygen conditions, organic components from biomass pyrolysis migrated in situ to cover the surface of lignite, resulting in a gradual smoothing of the fuel surface and a decrease in the specific surface area. Meanwhile, water reabsorption experiments and contact angle measurements showed that the equilibrium water holding capacity and water absorption capacity of the lifted fuels was weakened, and hydrophobicity was enhanced. Combustion kinetic parameters and pollutant release characteristics were investigated by thermogravimetric analysis (TGA) and isothermal combustion tests. It was found that co-upgradation could effectively reduce the reaction activation energy and NO conversion rate. Characterized by Raman spectroscopy (Raman) and X-ray photoelectron spectroscopy (XPS), in situ migration of organic components affected combustion reactivity by modulating changes in N-containing product precursors. The results showed that the extracted fuel with a 75% biomass blending ratio in the flue gas atmosphere exhibited the best overall performance at 220 °C, with optimal calorific value, combustion reactivity, and hydrophobicity. These findings may provide important theoretical foundations and practical guidance for the optimization of industrial-scale upgrading processes of low-quality fuels. Full article

Thermogravimetric analysis (TGA) is a key technique for evaluating the kinetics and thermodynamics of thermal degradation, providing essential data for material assessment and system design. When coupled with Fourier-transform infrared (FT-IR) spectroscopy or mass spectroscopy (MS), it enables the identification of evolved gases and correlates mass loss with specific chemical species, offering detailed insight into decomposition mechanisms. In this study, TGA was coupled with FT-IR and MS to investigate the thermal degradation behavior of Bakelite, with the aim of evaluating its kinetic and thermodynamic parameters under non-isothermal conditions, identifying evolved volatile compounds, and elucidating the degradation process. The results showed that higher heating rates led to increased decomposition temperatures and broader dTG peaks due to thermal lag effects. The degradation proceeded in multiple stages between 220 °C and 860 °C, ultimately yielding a carbonaceous residue. The activation energy increased with conversion, particularly beyond 0.5, indicating a greater energy requirement as degradation progressed. Peak values at conversion degrees of 0.8–0.9 suggested enhanced thermal stability or changes in the dominant reaction mechanism. Detailed kinetic analysis revealed complex decomposition pathways with variable activation energies and a pronounced kinetic compensation effect. Thermodynamic analysis confirmed the endothermic nature of the process, with increasing energy demand and non-spontaneous degradation of the resulting char. TGA/FT-IR and TGA/MS analyses identified the release of several compounds, including CO₂, water, formaldehyde, and phenolic derivatives, at distinct stages. This comprehensive understanding of Bakelite’s thermal behavior supports its optimization for high-temperature applications, enhances material reliability and safety, and contributes to sustainable processing and recycling strategies. Full article

This study presents a detailed and comprehensive investigation into the macro-scale performance, strength gain mechanisms, environment and economic performance of graphene oxide (GO)-enhanced low-emission concrete. A comprehensive experimental program evaluated fresh and hardened properties, including slump retention, bleeding, air content, compressive, flexural, and tensile strength, drying shrinkage, and elastic modulus. Scanning Electron Microscopy (SEM), energy-dispersive spectroscopy (EDS), Thermogravimetric analysis (TGA) and proton nuclear magnetic resonance (¹H-NMR) was employed to examine microstructural evolution and early age water retention, confirming GO’s role in accelerating cement hydration and promoting C-S-H formation. Optimal performance was achieved at 0.05% GO (by binder weight), resulting in a 25% increase in 28-day compressive strength without compromising workability. This outcome is attributed to a tailored, non-invasive mixing strategy, wherein GO was pre-dispersed during synthesis and subsequently blended without the use of invasive mixing methods such as high shear mixing or ultrasonication. Fourier-transform infrared (FTIR) spectroscopy further validated the chemical compatibility of GO and PCE and confirmed the compatibility and efficiency of the admixture. Sustainability metrics, including embodied carbon and strength-normalized cost indices (USD/MPa), indicated that, although GO increased material cost, the overall cost-performance ratio remained competitive at breakeven GO prices. Enhanced efficiency also led to lower net embodied CO₂ emissions. By integrating mechanical, microstructural, and environmental analyses, this study demonstrates GO’s multifunctional benefits and provides a robust basis for its industrial implementation in sustainable infrastructure. Full article

This study presents the development and characterization of electrospun nanofibers composed of polyvinyl alcohol (PVA) and natural beeswax (BW). A stable emulsion containing 9 wt% PVA and 5 wt% BW was successfully formulated and electrospun. The effects of beeswax incorporation on solution properties-viscosity, conductivity, and surface tension—were systematically evaluated. Electrospinning was performed at 30 kV and a working distance of 14.5 cm, yielding nanofibers with diameters between 125 and 425 nm. Scanning electron microscopy (SEM) revealed increased surface roughness and diameter variability in PVA/BW fibers compared to the PVA. Fourier transform infrared spectroscopy (FTIR) confirmed physical incorporation of BW without evidence of chemical bonding. Thermogravimetric and differential scanning calorimetry analyses (TGA/DSC) demonstrated altered behavior and an expanded profile of temperature transitions due to the waxy components. The solubility test of the nanofiber mat in saline indicated that BW slows dissolution and improves the structural integrity of the fibers. This study demonstrates, for the first time, the incorporation of beeswax into electrospun PVA nanofibers with improved structural and thermal properties, indicating potential for further exploration in biomedical material design. Full article

Polystyrene (PS), a thermoplastic polymer, is used in many applications due to its mechanical performance, good chemical inertness, and excellent processability. However, it is doped with different nanomaterials for reasons such as improving its electrical conductivity and mechanical properties. In this study, carbon nanotube (CNT)-added PS composites were produced with the aim of combining the properties of CNTs, such as their low weight and high tensile strength and Young’s modulus, with the versatility, processability, and mechanical properties of PS. In this study, multi-walled carbon nanotube (MWCNT)-reinforced polystyrene (PS) composites with different percentage ratios (0.1, 0.2, and 0.3 wt%) were prepared by a plastic injection molding method. The mechanical, microstructural, and thermal properties of the fabricated PS/MWCNT composites were characterized by Scanning Electron Microscopy (SEM), Fourier Transform Infrared (FTIR) Spectroscopy, Atomic Force Microscopy (AFM) and Thermogravimetric Analysis (TGA) techniques. AFM analyses were carried out to investigate the surface properties of MWCNT-reinforced composite materials by evaluating the root mean square (RMS) values. These analyses show that the RMS value for MWCNT-reinforced composite materials decreases as the weight percentage of MWCNTs increases. The TGA results show that there is no change in the degradation temperature of the 0.1%- and 0.2%-doped MWCNT composites compared to pure polystyrene, but the degradation of the 0.3%-doped MWCNT composite is almost complete at a temperature of 539 °C. Among the PS/MWCNT composites, the 0.3%-doped MWCNT composite exhibits more thermal stability than pure PS and other composites. Similarly, the values of the percentage elongation and tensile strength of 0.3% MWCNT-doped composites was obtained as 1.91% and 12.174% mm², respectively. These values are higher than the values of 0.1% and 0.2% MWCNT-doped composite materials. In conclusion, the mechanical and thermal properties of MWCNT-reinforced PS polymers provide promising results for researchers working in this field. Full article