Search Results (217)

Dynamic covalent bonds within polymer materials have been the subject of ongoing research. These bonds impart polymers, particularly thermosets, with capabilities for self-healing and reprocessing. Concurrently, three-dimensional (3D) printing techniques have undergone rapid advancement and widespread adoption. Since polymers are among the primary materials used in 3D printing, networks featuring dynamic covalent bonds have emerged as a prominent research area. This review outlines approaches for incorporating dynamic covalent bonds into polymers suitable for 3D printing and examines representative studies that leverage these chemistries in material design. Polymers produced using these strategies demonstrate both self-healing and reprocessability, primarily via bond-exchange (metathesis) reactions. In addition, we discuss how the type and amount of dynamic bonds in the network affect the resulting material properties, with particular emphasis on their mechanical, physical, and thermal performance. In particular, the introduction of dynamic covalent bonds seems to significantly improve the degree of anisotropy, which has been the limitation of 3D printing techniques. Finally, we compile recent applications for objects printed from polymers that include dynamic covalent bonds. Full article

To investigate the long-term water stability of graphene-modified permeable asphalt mixtures, in this study, we analysed the effects of single factors and multi-factor coupling. The single-factor water stability was investigated through the free thawing splitting test, standard Cantabro test, and immersion Cantabro test; the experimental indicators were the freeze–thaw cracking ratio (TSR), mass loss rate, and immersion mass loss rate, respectively. The multi-factor water stability was studied through immersion operation tests of mixtures with different degrees of ageing. The dispersion of graphene was examined through Raman mapping, the formation of three-dimensional network structures of graphene and SBS was evaluated via the dynamic shear rheometer test (DSR), and the elemental distribution was quantitatively analysed using energy-dispersive spectroscopy (EDS) and an image pixel algorithm (RGB). The results indicate that an unaged graphene-composite- and SBS-modified permeable asphalt mixture with an optimal graphene content of 0.05% demonstrated a 4.5% improvement in the TSR, alongside reductions in the mass loss rate and water immersion mass loss rate of 25.64% and 23.52%, respectively. Even after prolonged thermal oxygen ageing, its TSR, mass loss rate, and water immersion mass loss rate improved by 5.1%, 23.04%, and 20.70%, respectively. Multi-factor coupling tests confirmed that the water stability met requirements under severe conditions, with better performance at high temperatures. Graphene was uniformly dispersed in the modified asphalt. The appearance of a plateau region at low frequencies in graphene-composite- and SBS-modified asphalt verified the formation of a three-dimensional network structure, and the oxygen content was positively correlated with deepening thermal oxidative ageing. Full article

Silica aerogels are highly attractive due to their outstanding properties, including their low density, ultralow thermal conductivity, large porosity, high optical transparency, and strong sorption activity. However, their inherent brittleness has limited widespread applications. Constructing a robust, highly porous three-dimensional network is critical to achieving the desired mechanical properties in aerogels. In this study, we introduce a novel synthesis route for fabricating lightweight and mechanically strong aerogels by incorporating poly(ethylene-co-vinyl alcohol) (EVOH) through thermally induced phase separation (TIPS). EVOH exhibits upper critical solution temperature (UCST) behavior in a mixture of isopropanol (IPA) and water, which can be utilized to reinforce the silica skeletal structure. Robust aerogels were prepared via the sol–gel process and TIPS method, followed by supercritical CO₂ drying, yielding samples with bulk densities ranging from 0.136 to 0.200 g/cm³. N₂ physisorption analysis revealed a mesoporous structure, with the specific surface area decreasing from 874 to 401 m²/g as EVOH content increased from 0 to 80 mg/mL. The introduced EVOH significantly enhanced mechanical performance, raising the flexural strength and compressive strength to 0.545 MPa and 18.37 MPa, respectively—far exceeding those of pure silica aerogel (0.098 MPa and 0.74 MPa). This work demonstrates the effectiveness of the TIPS strategy for developing high-strength, low-density silica aerogels with well-preserved porosity. Full article

This paper presents a comprehensive analysis of the thermal stability and decomposition mechanisms of IPN hydrogels based on polyvinyl alcohol (PVA) and a copolymer network of poly(ethylene glycol) diacrylate–poly(ethylene glycol) methacrylate (PEGDA–PEGMA). Using thermogravimetric analysis (TGA/DTG) and multi-approach kinetic analysis (Friedman and Ozawa–Flynn–Wall isoconversion methods, nonparametric kinetics, Shestaka-Berggren model), the influence of composition on the processes of dehydration, thermal destruction, and the distribution of activation energy by degrees of conversion was investigated. The constructed three-dimensional kinetic “landscapes” made it possible to identify characteristic features of the behavior of various samples, including differences in the rate and mechanisms of destruction. It was found that an increase in the content of PVA enhances moisture binding and shifts the T_max of dehydration to higher temperatures, while an increase in the concentration of PEGDA forms a denser network that limits moisture retention and accelerates thermal decomposition. Calculation of diffusion coefficients using the Fick model showed a decrease in D with an increase in network density, which reflects an increase in resistance to moisture mass transfer. The combination of the data obtained demonstrates the multistage nature of thermal destruction and allows for the targeted selection of hydrogel compositions for biomedical, environmental, and materials science applications, including drug delivery systems, sorbents and heat-resistant coatings. Full article

With the continuous progress and innovation of petroleum engineering technology, the development of new oilfield additives with superior environmental benefits has attracted widespread attention. Konjac glucomannan (KGM) is a natural resource characterized by abundant availability, low cost, biodegradability, and environmental compatibility. Konjac gum easily forms a weak gel network in water, but its water solubility and thermal stability are poor, and it is easily degraded at high temperatures. Therefore, its application in drilling fluid and fracturing fluid is limited. In this paper, a method of carboxymethyl modification of KGM was developed, and a carboxymethyl group was introduced to adjust KGM’s hydrogel forming ability and stability. Carboxymethylated Konjac glucomannan (CMKG) is a water-soluble anionic polysaccharide derived from natural Konjac glucomannan. By introducing carboxymethyl groups, CMKG overcomes the limitations of the native polymer, such as poor solubility and instability, while retaining its safe and biocompatible nature, making it an effective natural polymer additive for oilfield applications. The results show that when used as a drilling fluid additive, CMKG can form a stable three-dimensional gel network through molecular chain cross-linking, significantly improving the rheological properties of the mud. Its unique gel structure can enhance the encapsulation of clay particles and inhibit clay hydration expansion. When used as a fracturing fluid thickener, the viscosity of the gel system formed by CMKG at 0.6% (w/v) is superior to that of the weak gel system of KGM. The heat resistance/shear resistance tests confirm that the gel structure remains intact under high-temperature and high-shear conditions, meeting the sand-carrying capacity requirements for fracturing operations. The gel-breaking experiment shows that the system can achieve controlled degradation within 300 min, in line with on-site gel-breaking specifications. This modification process not only improves the rheological properties and water solubility of the CMKG gel but also optimizes the gel stability and controlled degradation through molecular structure adjustment. Full article

Hydrogels comprise three-dimensional networks of hydrophilic polymers and have attracted considerable interest in various sectors, including the biomedical, pharmaceutical, agricultural, and food industries. These materials offer significant benefits for food packaging applications, such as high mechanical strength and excellent water absorption capacity, thereby contributing to the extension of product shelf life. Therefore, the aim of this study is to compare the performance of citric acid and glutaraldehyde as crosslinking agents in gelatine-based hydrogels reinforced with cellulose nanocrystals (CNC), contributing to the development of safe and environmentally responsible materials. The hydrogels were prepared using the casting method and characterised in terms of their physical, mechanical, and structural properties. The results indicated that hydrogels crosslinked with glutaraldehyde exhibited higher opacity, lower transparency, and greater mechanical strength, whereas those crosslinked with citric acid demonstrated improved clarity, reduced water permeability, and enhanced swelling capacity. The incorporation of CNC further improved mechanical strength, reduced weight loss, and altered both surface homogeneity and optical properties. Microstructural results obtained by SEM were consistent with the mechanical properties evaluated (TS, %E, and EM). The Gel-ca hydrogel displayed the highest elongation value (98%), reflecting better cohesion within the polymeric matrix. In contrast, films incorporating CNC exhibited greater roughness and cracking, which correlated with increased rigidity and mechanical strength, as evidenced by the high Young’s modulus (420 MPa in Gel-ga-CNC2). These findings suggest that the heterogeneity and porosity induced by CNC limit the mobility of polymer chains, resulting in less flexible and more rigid structures. Additionally, the DSC analysis revealed that gelatine hydrogels did not exhibit a well-defined Tg, due to the predominance of crystalline domains. Systems crosslinked with citric acid showed greater thermal stability (higher Tm and ΔH_m values), while those crosslinked with glutaraldehyde, although mechanically stronger, exhibited lower thermal stability. These results confirm the decisive effect of the crosslinking agent and CNC incorporation on the structural and thermal behaviour of hydrogels. In this context, the application of hydrogels in packaged products represents an eco-friendly alternative that enhances product presentation. This research supports the reduction in plastic consumption whilst promoting the principles of a circular economy and facilitating the development of materials with lower environmental impact. Full article

Conventional fracturing fluids, while essential for large-volume stimulation of unconventional reservoirs, often induce significant reservoir damage through water retention and capillary trapping. To address this problem, this study developed a novel superhydrophobic nano-viscous drag reducer (SN-DR), synthesized through a multi-monomer copolymerization and silane modification strategy, which enhances structural stability and minimizes reservoir damage. The structure and thermal stability of SN-DR were characterized by FT-IR, ¹H NMR, and TGA. Rheological evaluations demonstrated that the gel fracturing fluid exhibits a highly stable three-dimensional network structure, with a G′ maintained at approximately 3000 Pa and excellent shear recovery under cyclic stress. Performance tests showed that a 0.15% SN-DR achieved a drag reduction rate of 78.1% at 40 L/min, reduced oil–water interfacial tension to 0.91 mN·m⁻¹, and yielded a water contact angle of 152.07°, confirming strong hydrophobicity. Core flooding tests revealed a flowback rate exceeding 50% and an average permeability recovery of 86%. SEM and EDS indicated that the gel formed nanoscale, tightly packed papillary structures on core surfaces, enhancing roughness and reducing water intrusion. The study demonstrates that gel fracturing fluid enhances structural stability, alters wettability, and mitigates water-blocking damage. These findings offer a new strategy for designing high-performance fracturing fluids with integrated drag reduction and reservoir protection properties, providing significant theoretical insights for improving hydraulic fracturing efficiency. Full article

The growing demand for efficient thermal management in power electronics and high-density optoelectronic systems necessitates thermal interface materials (TIMs) with high through-plane thermal conductivity and minimal anisotropy. However, conventional polymer composites filled with platelet-type fillers such as hexagonal boron nitride (h-BN) suffer from strong directional thermal transport and interfacial resistance, limiting their practical effectiveness. To address this limitation, we present a hybrid filler strategy wherein h-BN and silicon carbide (SiC) nanoparticles interact via hydroxylated surfaces, forming a three-dimensional thermally conductive network. The resulting BN–SiC composite exhibits enhanced through-plane thermal conductivity (1.61 W/mK at 70 vol%) and lower anisotropy ratios (<2.0 at 30 vol%), all while maintaining mechanical integrity and processability. These results demonstrate that chemical bonding at the filler interface can reduce interfacial thermal resistance and extend thermal conduction paths three-dimensionally, providing insights into interface-based heat transfer mechanisms. This strategy presents a scalable and practical approach for next-generation thermal management solutions in electronic packaging and high-power device platforms. Full article

Carboxymethyl chitosan (CMC)-based hydrogels have emerged as promising candidates for wound dressing applications due to their excellent biocompatibility and tunable physicochemical properties. In this study, a novel hydrogel functionalized with hyaluronic acid (HA) and RGD peptides (RGD) was fabricated and evaluated for its structural characteristics and wound-healing potential. Using CMC as the base matrix and EDC/NHS as crosslinking agents, four hydrogel variants were fabricated: CMC gel, CMC-HA gel, CMC-RGD gel, and CMC-HA-RGD gel. The preliminary cell compatibility experiment identified the optimal formulation as 1% CMC, 0.9% HA, and 0.02 mg/mL RGD, crosslinked with 1 vol% EDC and 0.05 wt% NHS. Scanning electron microscopy showed a porous architecture (100–400 μm), conducive to fibroblast viability and proliferation. Zeta potential measurements (|ζ| > 30 mV) indicated colloidal stability of the hydrogel system. Fourier-transform infrared spectroscopy confirmed successful crosslinking and integration of HA and RGD via hydrogen bonding and electrostatic interactions, forming a stable three-dimensional network. Thermogravimetric analysis revealed enhanced thermal stability upon HA/RGD incorporation. CCK-8 assays demonstrated significantly improved cell viability with HA/RGD loading (p < 0.05), while Ki-67 immunofluorescence confirmed enhanced fibroblast proliferation, with the CMC-HA-RGD gel showing the most pronounced effect. In vitro scratch assay results demonstrated that the CMC-HA-RGD hydrogel dressing significantly enhanced cellular migration compared to other carboxymethyl chitosan-based hydrogel groups (p < 0.05). The observed statistically significant improvement in cell migration rate versus controls underscores the distinctive enhancement of synergistic HA and RGD modification in accelerating cellular migration and facilitating wound repair. Collectively, these findings suggest that the CMC-HA-RGD hydrogel possesses favorable physicochemical and biological properties and holds strong potential as an advanced wound dressing for the treatment of chronic and refractory wounds. Full article

Dynamic Line Rating (DLR) is increasingly important for maximizing capacity of existing overhead transmission lines. Conventional thermal rating methods, such as IEEE 738 and model conductors as single, isothermal cylinders and offer limited guidance for multi-conductor bundles, not fully capturing the complex aerodynamic and thermal interactions present in high-voltage networks. This study addresses these limitations by presenting a high-fidelity, two-dimensional coupled thermal-fluid model developed in COMSOL Multiphysics 4.3b. Single and bundled configurations (two-conductor, three-conductor and four-conductor) are analyzed under steady-state conditions using the Shear Stress Transport (SST) turbulence model, accounting for sub-conductor spacing, wind speed, and interactions between temperature distribution and airflow. Simulation results are compared with ampacity calculations from relevant standards to evaluate limitations of simplified models. Results show that leeward conductors reach temperatures up to ~4 °C higher than windward conductors, forming the thermal bottleneck, with peak temperatures of ~103.3 °C versus ~99 °C for single conductors. For bundled conductors, the current required to keep the maximum temperature at 100 °C was calculated, and this value was found to be approximately 3% lower than the current predicted by IEEE 738. The study emphasizes the importance of multiphysics, position-aware simulations to prevent overloading and optimize transmission line utilization. Full article

The Super-long Gravity Heat Pipe (SLGHP) is an efficient geothermal energy utilization technology that can transmit thermal energy by fully utilizing natural temperature differences without external energy input. This study focuses on the high-altitude geothermal environment of Mount Meager, Canada, and employs numerical simulations and dynamic thermal analysis to systematically investigate the thermal transport performance of the SLGHP system under both steady-state and dynamic operating conditions. The study also examines the impact of various structural parameters on the system’s performance. Three-dimensional CFD simulations were conducted to analyze the effects of pipe diameter, length, filling ratio, working fluid selection, and pipe material on the heat transfer efficiency and heat flux distribution of the SLGHP. The results indicate that working fluids such as CO₂ and NH₃ significantly enhance the heat flux density, while increasing pipe diameter may reduce the amount of liquid retained in the condenser section, thereby affecting condensate return and thermal stability. Furthermore, dynamic thermal analysis using a three-node RC network model simulated the effects of diurnal temperature fluctuations and variations in the convective heat transfer coefficient in the condenser section on system thermal stability. The results show that the condenser heat flux can reach a peak of 5246 W/m² during the day, while maintaining a range of 2200–2600 W/m² at night, with the system exhibiting good thermal responsiveness and no significant lag or flow interruption. In addition, based on the thermal output of the SLGHP system and the integration with the Organic Rankine Cycle (ORC) system, the power generation potential analysis indicates that the system, with 100 heat pipes, can provide stable power generation of 50–60 kW. In contrast to previous SLGHP studies focused on generalized modeling, this work introduces a site-specific CFD–RC framework, quantifies structural sensitivity via heat flux indices, and bridges numerical performance with economic feasibility, offering actionable insights for high-altitude deployment. This system has promising practical applications, particularly for providing stable renewable power in remote and cold regions. Future research will focus on field experiments and system optimization to further improve system efficiency and economic viability. Full article

This study aimed to develop a novel biomaterial for neural tissue regeneration by combining chitosan (CS), a natural polymer, with graphene oxide (GO) at concentrations of 3%, 6%, and 9%. The homogeneity, conductivity, three-dimensional characteristics, and ability to support cell viability of the composite materials were systematically evaluated. Fourier-Transform Infrared (FTIR) spectroscopy confirmed the successful incorporation of GO into the CS matrix, while UV-Vis and photoluminescence (PL) spectrometry revealed modifications in the optical properties with increasing GO content. Thermogravimetric analysis (TG-DSC) demonstrated improved thermal stability of the composites, and swelling tests indicated enhanced water absorption capacity. Although some agglomerates were observed, the homogeneity was reasonable at both macroscopic and microscopic level (optical visualization–FTIR and electron microscopy). The composite films exhibited promising physical and electrochemical properties, highlighting their potential for neural tissue engineering applications. Their biological activity was assessed by culturing neuronal cells on the CS-GO scaffolds. Results from MTT, LDH, and LIVE/DEAD assays demonstrated excellent cell viability, moderate-to-good cell attachment, and the promotion of intercellular network formation. Among the tested formulations, the CS-GO 6% scaffold showed the most favorable biological response, with a significant increase in SH-SY5Y cell viability after 7 days (p < 0.05) compared to the CS control. LIVE/DEAD imaging confirmed enhanced cell attachment and elongated morphology, while the LDH assay indicated minimal cytotoxicity. Notably, a critical threshold was identified between 6% and 9% GO, where conductivity increased by approximately 52-fold. Future studies should focus on optimizing the composite parameters, loading them with specific biologically active agents and thus targeting specific neuronal applications. Full article

The safe and efficient capture of CO₂ in confined environments such as coal mine goafs remains a significant challenge, posing both environmental and safety risks. To address this issue, this study developed a novel biomass-based aerogel adsorbent using CNF-C and CS through sol–gel synthesis and freeze-drying. A series of composite aerogels with varying mass ratios were systematically characterized by SEM, BET, FTIR, and TG-DSC to analyze their microstructure, specific surface area, pore characteristics, chemical properties, and thermal stability. A constant temperature and humidity experimental setup was specially designed to explore the effects of various temperatures, humidity, and material ratios on CO₂ adsorption performance. FTIR analysis confirmed that -NH₂ served as the primary adsorption site, with its density increasing with higher chitosan content. The 1:3 ratio exhibited the optimal specific surface area (7.05 m²/g) and thermal stability, withstanding temperatures up to 350.0 °C, while the 1:1 ratio demonstrated the highest porosity (80.74%). Adsorption experiments indicated that 35.0 °C and 50% humidity were the optimal conditions, under which the 1:2 ratio biomass aerogel achieved an 18% increase in CO₂ adsorption capacity compared to room temperature. The sample with a 1:1 high cellulose ratio is primarily dominated by physical adsorption, making its performance susceptible to environmental fluctuations. The sample with a 1:3 high chitosan ratio is predominantly governed by chemical adsorption, exhibiting more stable adsorption characteristics. The 1:2 ratio achieved the best balance under 35.0 °C and 50% humidity. The biomass aerogel synergistically combined physical barriers from its three-dimensional network structure and chemical adsorption via active functional groups, enabling efficient CO₂ capture and stable sequestration. This study demonstrates the feasibility of biomass-derived aerogels for CO₂ adsorption under complex conditions and provides new insights into the design of sustainable materials for environmental remediation and carbon reduction applications. Full article

Polymers derived from renewable polysaccharides offer promising avenues for the development of high-temperature, environmentally friendly drilling fluids. However, their industrial application remains limited by inadequate thermal stability and poor colloidal compatibility in complex mud systems. In this study, we report the rational design and synthesis of epichlorohydrin-crosslinked carboxymethyl xylan (ECX), developed through a synergistic strategy combining covalent crosslinking with hydrophilic functionalization. When incorporated into water-based drilling fluid base slurries, ECX facilitates the formation of a robust gel suspension. Comprehensive structural analyses (FT-IR, XRD, TGA/DSC) reveal that dual carboxymethylation and ether crosslinking impart a 10 °C increase in glass transition temperature and a 15% boost in crystallinity, forming a rigid–flexible three-dimensional network. ECX-modified drilling fluids demonstrate excellent colloidal stability, as evidenced by an enhancement in zeta potential from −25 mV to −52 mV, which significantly improves dispersion and interparticle electrostatic repulsion. In practical formulation (1.0 wt%), ECX achieves a 620% rise in yield point and a 71.6% reduction in fluid loss at room temperature, maintaining 70% of rheological performance and 57.5% of filtration control following dynamic aging at 150 °C. Tribological tests show friction reduction up to 68.2%, efficiently retained after thermal treatment. SEM analysis further confirms the formation of dense and uniform polymer–clay composite filter cakes, elucidating the mechanism behind its high-temperature resilience and effective sealing performance. Furthermore, ECX demonstrates high biodegradability (BOD₅/COD = 21.3%) and low aquatic toxicity (EC₅₀ = 14 mg/L), aligning with sustainable development goals. This work elucidates the correlation between molecular engineering, gel microstructure, and macroscopic function, underscoring the great potential of eco-friendly polysaccharide-based crosslinked polymers for industrial gel-based fluid design in harsh environments. Full article

Snow and ice accumulation on transportation infrastructure presents significant safety and maintenance challenges in cold regions, while conventional removal methods are both energy-intensive and environmentally detrimental. This study proposes a passive Heat Pipe–Coupled Geothermal Snow Melting System (HP-GSMS) that harnesses shallow geothermal energy to maintain snow-free surfaces without external energy input. Using Fluent-based CFD simulations, the system’s thermal performance was evaluated under various working fluids (ammonia, carbon dioxide, water) and pipe materials (stainless steel, aluminum). A one-dimensional thermal resistance model validated the CFD results under ammonia–stainless steel conditions, predicting a heat flux of 358.6 W/m² compared to 361.0 W/m² from the simulation, with a deviation of only 0.66%, confirming model accuracy. Ammonia demonstrated superior phase-change efficiency, with the aluminum–ammonia configuration yielding the highest heat flux (up to 677 W/m²), surpassing typical snow-melting thresholds. Aluminum pipes enhanced radial heat conduction without compromising phase stability, while water exhibited poor phase-change performance and CO₂ showed moderate but stable behavior. Additionally, a dynamic three-node RC thermal network was employed to assess transient performance under realistic diurnal temperature variations, revealing surface heat fluxes ranging from 230 to 460 W/m², with a daily average of approximately 340 W/m². These findings demonstrate the HP-GSMS’s practical viability in cold climates and underscore the importance of selecting low-boiling-point fluids and high-conductivity materials for scalable, energy-efficient, and low-carbon snow-melting applications in urban infrastructure. Full article