Search Results (102)

Deep coalbed methane (CBM) reservoirs are characterized by high hydrocarbon content and are considered an important strategic resource. Due to their inherently low permeability and porosity, horizontal well drilling is commonly employed to enhance production, with the length of the horizontal section playing a critical role in determining CBM output. However, during extended horizontal drilling, wellbore instability frequently occurs as a result of drilling fluid invasion into the coal formation, posing significant safety challenges. This instability is primarily caused by the physical intrusion of drilling fluids and their interactions with the coal seam, which alter the mechanical integrity of the formation. To address these challenges, interpenetrating and semi-interpenetrating network (IPN/s-IPN) hydrogels have gained attention due to their superior physicochemical properties. This material offers enhanced sealing and support performance across fracture widths ranging from micrometers to millimeters, making it especially suited for plugging applications in deep CBM reservoirs. A self-degradable interpenetrating double-network hydrogel particle plugging agent (SSG) was developed in this study, using polyacrylamide (PAM) as the primary network and an ionic polymer as the secondary network. The SSG demonstrated excellent thermal stability, remaining intact for at least 40 h in simulated formation water at 120 °C with a degradation rate as high as 90.8%, thereby minimizing potential damage to the reservoir. After thermal aging at 120 °C, the SSG maintained strong plugging performance and favorable viscoelastic properties. A drilling fluid containing 2% SSG achieved an invasion depth of only 2.85 cm in an 80–100 mesh sand bed. The linear viscoelastic region (LVR) ranged from 0.1% to 0.98%, and the elastic modulus reached 2100 Pa, indicating robust mechanical support and deformation resistance. Full article

Background/Objectives: Photothermal therapy (PTT) is an emerging minimally invasive strategy in biomedicine that converts near-infrared (NIR) light into localized heat for the targeted inactivation of pathogens and tumor cells. Methods and Results: In this study, we report the synthesis and characterization of thermoresponsive nanogels composed of poly (N-isopropylacrylamide-co-N-isopropylmethylacrylamide) (PNIPAM-co-PNIPMAM) semi-interpenetrated with polypyrrole (PPy), yielding monodisperse particles of 377 nm diameter. Spectroscopic analyses—including ¹H-NMR, FTIR, and UV-Vis—confirmed successful copolymer formation and PPy incorporation, while TEM images revealed uniform spherical morphology. Differential scanning calorimetry established a volumetric phase transition temperature of 38.4 °C, and photothermal assays demonstrated a ΔT ≈ 10 °C upon 10 min of 850 nm NIR irradiation. In vitro antimicrobial activity tests against Pseudomonas aeruginosa (ATCC 15692) showed a dose-time-dependent reduction in bacterial viability, with up to 4 log CFU/mL. Additionally, gentamicin-loaded nanogels achieved 38.7% encapsulation efficiency and exhibited stimulus-responsive drug release exceeding 75% under NIR irradiation. Conclusions: Combined photothermal and antibiotic therapy yielded augmented bacterial killing, underscoring the potential of PPy-interpenetrated nanogels as smart, dual-mode antimicrobials. Full article

Polygalacturonic acid (PGA), derived from the natural plant polysaccharide, pectin, has been suggested as a biomaterial for implantable medical devices and tissue engineering; particularly in the field of bone implant materials. As a negatively charged polysaccharide, PGA can be considered similar to hyaluronic acid, a component of the extracellular matrix (ECM). PGA-based biomaterials may therefore exhibit favorable biocompatibility with surface chemistry mimicking the natural ECM. In this study, we synthesized semi-interpenetrating polymer networks (SIPNs) incorporating PGA, and conducted physical characterization and in vitro biocompatibility studies. Biocompatibility testing revealed the SIPNs to be cytocompatible, with the PGA component conferring some resistance to the adherence of the macrophage cell line RAW264.7. In addition, SIPNs did not support the fusion of primary murine macrophages into foreign body giant cells (FBGCs). Macrophage adherence and FBGC formation on implanted biomaterial surfaces are important events in the progression of a foreign body response. Our in vitro studies suggest that PGA-based materials may offer desirable biocompatibility profiles, holding promise for future clinical applications. Full article

Cellulose, a widely abundant natural polymer, is well recognized for its remarkable properties, such as biocompatibility, degradability, and mechanical strength. Conductive hydrogels, with their unique ability to conduct electricity, have attracted significant attention in various fields. The combination of cellulose and conductive hydrogels has led to the emergence of cellulose-based conductive hydrogels, which show great potential in flexible electronics, biomedicine, and energy storage. This review article comprehensively presents the latest progress in cellulose-based conductive hydrogels. Firstly, it provides an in-depth overview of cellulose, covering aspects like its structure, diverse sources, and classification. This emphasizes cellulose’s role as a renewable and versatile material. The development and applications of different forms of cellulose, including delignified wood, bacterial cellulose, nanocellulose, and modified cellulose, are elaborated. Subsequently, cellulose-based hydrogels are introduced, with a focus on their network structures, such as single-network, interpenetrating network, and semi-interpenetrating network. The construction of cellulose-based conductive hydrogels is then discussed in detail. This includes their conductive forms, which are classified into electronic and ionic conductive hydrogels, and key performance requirements, such as cost-effectiveness, mechanical property regulation, sensitive response to environmental stimuli, self-healing ability, stable conductivity, and multifunctionality. The applications of cellulose-based conductive hydrogels in multiple areas are also presented. In wearable sensors, they can effectively monitor human physiological signals in real time. In intelligent biomedicine, they contribute to wound healing, tissue engineering, and nerve regeneration. In flexible supercapacitors, they offer potential for green and sustainable energy storage. In gel electrolytes for conventional batteries, they help address critical issues like lithium dendrite growth. Despite the significant progress, there are still challenges to overcome. These include enhancing the multifunctionality and intelligence of cellulose-based conductive hydrogels, strengthening their connection with artificial intelligence, and achieving simple, green, and intelligent large-scale industrial production. Future research directions should center around exploring new synthesis methods, optimizing material properties, and expanding applications in emerging fields, aiming to promote the widespread commercialization of these materials. Full article

Industrial textile wastewater containing both heavy metals and dyes has been massively produced. In this study, semi-interpenetrating polymer network structures of sodium alginate (SA)/polyvinyl alcohol (PVA)/κ-carrageenan (CG) aerogel beads were synthesized for their simultaneous reduction. The SA/PVA/CG aerogel beads were synthesized through a cost-effective and environmentally friendly method using naturally abundant biopolymers without toxic cross-linkers. The SA/PVA/CG aerogel beads were spheres with a size of 3.8 $\pm$ 0.1 mm, exhibiting total pore areas of 15.2 m²/g and porous structures (pore size distribution: 0.04–242.7 μm; porosity: 93.97%) with abundant hydrogen bonding, high water absorption capacity, and chemical resistance. The adsorption capacity and mechanisms of the SA/PVA/CG aerogel beads were investigated through kinetic and isotherm experiments for heavy metals (Cu(II), Pb(II)), cationic dye (methylene blue, MB), and anionic dye (acid blue 25, AB)) in both single and binary systems. The maximum adsorption capacities of the SA/PVA/CG aerogel beads based on the Langmuir model of Cu(II), Pb(II), and MB were 85.17, 265.98, and 1324.30 mg/g, respectively. Pb(II) showed higher adsorption affinity than Cu(II) based on ionic properties, such as electronegativity and hydration radius. The adsorption of Cu(II), Pb(II), and MB on the SA/PVA/CG aerogel beads was spontaneous, with heavy metals and MB exhibiting endothermic and exothermic natures, respectively. Full article

Purpose: To fabricate 3D-printed, biodegradable conjunctival gelatin methacrylate (GelMA) inserts that can release polyvinyl alcohol (PVA) when exposed to an ocular surface enzyme. Method: In this work, biodegradable conjunctival inserts were 3D-printed using a stereolithography-based technique. The release of PVA from these insert formulations (containing 10% GelMA and 5% PVA (P-Gel-5%)) was assessed along with different mathematical models of drug release. The biodegradation rates of these inserts were studied in the presence of a tear-film enzyme (matrix metalloproteinase-9; MMP9). The morphology of the inserts before and after enzymatic degradation was monitored using scanning electron microscopy. Results: The 3D-printed P-Gel-5% inserts formed a semi-interpenetrating network, which was mechanically stronger than GelMA inserts. The PVA release graphs demonstrate that at the end of 24 h, 222.7 ± 20.3 µg, 265.5 ± 27.1 µg, and 242.7 ± 30.4 µg of PVA were released when exposed to 25, 50, and 100 µg/mL of MMP9, respectively. The release profiles of the P-Gel-5% containing hydrogels in the presence of different concentrations of MMP9 showed the highest linearity with the Korsmeyer–Peppas model. The results suggest that the degradation rate over 24 h is a function of MMP9 enzyme concentration. Over 80% of P-Gel-5% inserts were degraded at the end of 8 h, 12 h, and 24 h in the presence of 100, 50, and 25 µg/mL MMP9 enzyme solutions, respectively. Conclusions: These results demonstrate the potential for 3D printing of GelMA for use as conjunctival inserts. These inserts could be used to deliver PVA, which is a well-known therapeutic agent for dry eye disease. PVA release is influenced by multiple mechanisms, including diffusion and enzymatic degradation, which is supported by morphological studies and biodegradation results. Full article

One of the emergent regenerative treatments for the restoration of the articular cartilage is tissue engineering (TE), in which hydrogels can functionally imitate the extracellular matrix (ECM) of the native tissue and create an optimal microenvironment for the restoration of the defective tissue. Hyaluronic acid (HA) is known for its potential in the field of TE as a regenerative material for many tissues. It is one of the major components of the articular cartilage ECM contributing to cell proliferation and migration. HA is the only non-sulphated glycosaminoglycan (GAG). However, herein, we use a HA presenting a high amount of sulphated glycosaminoglycans (sGAGs), altering the intrinsic properties of the material particularly in terms of biological response. Alginate (Alg) is another polysaccharide widely used in TE that allows stiff and stable hydrogels to be obtained when crosslinked with CaCl₂. Taking the benefit of the favourable characteristics of each biomaterial, semi-interpenetrating (semi-IPN) hydrogels had been developed by the combination of both materials, in which alginate is gelled, and HA remains uncrosslinked within the hydrogel. Varying the concentration of alginate and HA, the final rheological, viscoelastic, and mechanical properties of the hydrogel can be tailored, always seeking a trade-off between biological and physico-mechanical properties. All developed semi-IPN hydrogels have great potential for biomedical applications. Full article

In this article, we report on the alginate heterografted by Poly(N-isopropyl acrylamide-co-N-tert-butyl acrylamide) and Poly(N-isopropyl acrylamide) (ALG-g-P(NIPAM86-co-NtBAM14)-g-PNIPAM) copolymer thermoresponsive hydrogel, reinforced by substituting part of the 5 wt% aqueous formulation by small amounts of Poly(acrylic acid)-g-P(boc-L-Lysine) (PAA-g-P(b-LL)) graft copolymer (up to 1 wt%). The resulting complex hydrogels were explored by oscillatory and steady-state shear rheology. The thermoresponsive profile of the formulations were affected remarkably by increasing the PAA-g-P(b-LL) component of the polymer blend. Especially, the sol-gel behavior altered to soft gel–strong gel behavior due to the formation of a semi-interpenetrating network based on the hydrophobic self-organization of the PAA-g-P(b-LL). In addition, the critical characteristics, namely T_{c,thermothickening} (temperature above which the viscosity increases steeply) and ΔT (transition temperature window), shifted and broadened to lower temperatures, respectively, due to the influence of the hydrophobic side chains P(b-LL) on the LCST of the PNIPAM-based grafted chains of the alginate. The effect of ionic strength was also examined, showing that this is another important factor affecting the thermoresponsiveness of the hydrogel. Again, the thermoresponsive profile of the hydrogel was changed significantly by the presence of salt. All the formulations showed self-healing capability and tolerance injectability, suitable for potential bioapplications in living bodies. Full article

Natural superabsorbent polymers (SAPs) were essential coating materials for developing slow-release fertilizers (SRFs) due to low cost and biodegradability. However, conventional natural SAPs were unsuitable for rice systems due to low stability and short slow-release period. Herein, a natural SAP with a semi-interpenetrating polymer network was prepared by poly (γ-glutamic acid) (PGlu), diatomite, and pullulan polysaccharide and combined with biochar to develop double-layer co-coated slow-release urea for rice systems. The results indicated that diatomite and pullulan modification significantly improved the slow-release capacity of SAP, with a significant increase in the average fertilizer ¹⁵N content of the soil profile by 37.9 ± 7.4% in 14–56 days. The improved slow-release capacity had significant benefits for the sustainability of the rice system, which increased plant N uptake by 17.2 ± 4.8%, decreased fertilizer N losses by 30.4 ± 7.2%, and increased rice grain yield by 9.88 ± 3.6%. More importantly, this natural SAP was fully degradable and its decomposition products are large amounts of small-molecule nutrients that could provide additional C, N, and Si to rice. Therefore, novel co-coated SRF may emerge as a greatly promising candidate for future intensive paddies. Full article

The need for new biomaterials to meet the needs of advanced healthcare therapies is constantly increasing. Polysaccharide-based matrices are considered extremely promising because of their biocompatibility and soft structure; however, their use is limited by their poor mechanical properties. In this light, a strategy for the reinforcement of dextran-based hydrogels and interpenetrated polymer networks (semi-IPNs and IPNs) is proposed, which will introduce multifunctional crosslinkers that can modify the network crosslinking density. Hydrogels were prepared via dextran methacrylation (DexMa), followed by UV photocrosslinking in the presence of diacrylate (NPGDA), triacrylate (TMPTA), and tetraacrylate (PETA) crosslinkers at different concentrations. The effect of these molecules was also tested on DexMa-gellan semi-IPN (DexMa/Ge) and, later, on IPN (DexMa/CaGe), obtained after solvent exchange with CaCl₂ in HEPES and the resulting Ge gelation. Mechanical properties were investigated via rheological and dynamic mechanical analyses to assess the rigidity, resistance, and strength of the systems. Our findings support the use of crosslinkers with different functionality to modulate the properties of polysaccharide-based scaffolds, making them suitable for various biomedical applications. While no significative difference is observed on enriched semi-IPN, a clear improvement is visible on DexMa and DexMa/CaGe systems when TMPTA and NPGDA crosslinker are introduced at higher concentrations, respectively. Full article

Solid-state electrolytes are widely anticipated to revitalize lithium-ion batteries with high energy density and safety. However, low ionic conductivity and high interfacial resistance at room temperature pose challenges for practical applications. This study combines the rigid oxide electrolyte LLZTO with the flexible polymer electrolyte poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) to achieve effective coupling of rigidity and flexibility. The semi-interpenetrating network structure endows the PEL composite solid electrolyte with excellent lithium-ion transport capabilities, resulting in an ionic conductivity of up to 5.1 × 10⁻⁴ S cm⁻¹ and lithium-ion transference number of 0.41. The assembled LiFePO₄/PEL/Li solid-state battery demonstrates an initial discharge capacity of 132 mAh g⁻¹ at a rate of 0.1 C. After 100 charge–discharge cycles, the capacity retention is 81%. This research provides a promising strategy for preparing composite solid electrolytes in solid-state lithium-ion batteries. Full article

This study successfully developed a bio-based, photocurable, anionic–nonionic dual-functional chain extender, and sulfonated cardanol-based polyethylene glycol (SCP), derived from renewable resources—cardanol and polyethylene glycol—for application in waterborne polyurethane dispersions (WPUDs). Utilizing SCP as a chain extender, WPUDs were prepared through a typical acetone process with poly(butylene adipate) (PBA), isophorone diisocyanate (IPDI), and ethylene diamine (EDA) at a constant NCO/OH ratio of 1:1. This research focused on the effects of polyethylene glycol molecular weight and SCP dosage on the particle size, stability, and film-forming properties of the WPUD. Optimal dispersion stability and film-forming performance were achieved with a polyethylene glycol molecular weight of 1500 and a PBA to SCP molar ratio of 4:1, yielding a particle size of 0.326 ± 0.010 μm and excellent storage stability over six months. The resulting WPU coatings exhibited a tensile strength of 11.4 MPa, which increased to 16.8 MPa after UV irradiation owing to the formation of a semi-interpenetrating network via the photopolymerization of cardanol’s unsaturated side chains. UV cross-linking also enhanced water resistance, reducing the water absorption rate (WAR) from 18.68% to 4.21% and the water vapor transmission rate (WVTR) from 6.59 × 10⁻⁵ g·m⁻¹·Pa⁻¹·d⁻¹ to 2.26 × 10⁻⁵ g·m⁻¹·Pa⁻¹·d⁻¹, while also improving thermal stability. These findings demonstrate that SCP offers a sustainable and effective solution for developing high-performance WPU coatings. Full article

Designing a wound dressing with controlled uptake, antibacterial, and proper biocompatibility is crucial for the appropriate wound healing process. In this study, alginate/tetracycline (Alg/TC) beads were produced and embedded into chitosan/pluronic/agarose semi-interpenetrating polymer network hydrogel, which serves as a potential biocompatible dressing for treating skin wounds. The effect of pluronic content on the porosity, swelling, mechanical characteristics, and degradation of the hydrogel was investigated. Furthermore, the impact of Alg beads on TC release was subsequently examined. In the absence of Alg beads, faster release was observed. However, after incorporating beads into the hydrogels, the release was sustained. Particularly, the hydrogel containing Alg beads exhibited a nearly linear release, reaching 74% after 2 days in acidic media. The antimicrobial activity and biocompatibility of the hydrogel were also evaluated to assess the capability of the TC-loaded hydrogels for wound dressing applications. The hydrogel demonstrated efficient antibacterial features against Gram-positive and Gram-negative bacteria. Additionally, the sample behavior was evaluated against exposure to yeast. Furthermore, based on biocompatibility studies using HFF2 cells, the TC-loaded hydrogel exhibited remarkable biocompatibility. Overall, this novel composite hydrogel shows remarkable biocompatibility and antibacterial activities which can be used as a great potential wound dressing to prevent wound infections due to its effective inhibition of bacterial growth. Full article

Amidoxime-functionalized hydrogels are one of most promising adsorbents for high-efficiency uranium (U) extraction from seawater, but bioadhesion on their surface seriously decreases their adsorption efficiency and largely shortens their service life. Herein, a semi-interpenetrating zwitterion–poly(amidoxime) (ZW-PAO) hydrogel was explored through introducing a PAO polymer into a poly [3-(dimethyl 4-vinylbenzyl amino) propyl sulfonate] (PDVBAP) polyzwitterionic (PZW) network via ultraviolet (UV) polymerization. Owing to the anti-polyelectrolyte effect of the PZW network, this ZW-PAO hydrogel can provide excellent super-hydrophilicity in seawater for high-efficiency U-adsorption from seawater. Furthermore, the ZW-PAO hydrogel had outstanding anti-biofouling performance for both highly enhanced U-adsorption and a relatively long working life in natural seawater. As a result, during only 25 days in seawater (without filtering bacteria), the U-uptake amount of this ZW-PAO hydrogel can reach 9.38 mg/g and its average rate can reach 0.375 mg/(g∙day), which is excellent among reported adsorbents. This work has explored a promising hydrogel for high-efficiency U-recovery from natural seawater and will inspire new strategy for U-adsorbing materials. Full article

An alternative synthetic pathway was proposed for the optimization of synthesis to find a better correlation between the swelling and elasticity of hyaluronic acid-interpenetrated gels via temperature regulation. An experimental design methodology was presented for the synthesis of polyacrylamide/poly(acrylic acid sodium salt)/hyaluronic acid, PAAm/PSA/HyA, gels by modifying the one-pot procedure using free radical crosslinking copolymerization of AAm with the addition of anionic linear PSA chains in the presence of various amount of HyA, ranging between 0.05% and 0.20% (w/v). Semi-interpenetrated polymer network (IPN)-structured gels were designed with tunable elasticity, in which the extent of covalent crosslinking interactions is controlled by polymerization temperature ranging between −18 and 45 °C. Depending on the HyA content added in the synthesis and the polymerization temperature, the swelling ratio could be controlled. The addition of 0.05% (w/v) HyA increased the swelling of semi-IPNs, while the elastic modulus increased with increasing HyA content and decreased with the polymerization temperature. PAAm/PSA/HyA semi-IPNs showed the typical pH-sensitive swelling of anionic gels, and the swelling reached a maximum at a pH of 11.2. PAAm/PSA/HyA gels were tested for the removal of methyl violet from wastewater. Adsorption kinetics were shown to be well-fitted with the pseudo-second-order model using linear and nonlinear regression analysis. With the clear relationship between increased modulus and composition, this study enabled the fine-tuning of semi-IPN interactions by varying the polymerization temperature. Full article