Search Results (181)

The design of hydrogel-based materials for wound care management requires the integration of multiple functionalities, including the capacity to maintain hydration, to prevent infection, and to adapt to the dynamic wound microenvironment. In this study, we fabricated innovative pH-reactive multilayer hydrogel patches based on ionically crosslinked alginate and incorporated with bioactive compounds, including Manuka honey, hyaluronic acid, and Ribes nigrum extract. The multilayer structure is coated with chitosan to improve water affinity and pH response. The patches are designed to respond to variable pH conditions typical of wound environments, with potential applicability to burn wounds. The hydrogel materials are characterized in terms of water content, swelling behavior, and water vapor transmission rate (WVTR). The chitosan-coated multilayer hydrogel exhibited high water uptake (swelling ratio up to 22.11 ± 0.25; water content 95.48 ± 0.05%) and controlled WVTR (~3450–3850 g/m²·day⁻¹), while degradation remained below 42% at pH 8 compared to >80% in single layers. Microstructural analysis is performed via optical microscopy to assess the morphology and uniformity of the multilayer system, while chemical characterization is conducted using Fourier-transform infrared (FTIR) spectroscopy. The results highlight the ability of the designed material to respond to pH variations and to accommodate bioactive agents within a structurally stable and hydrated network, suggesting its suitability for future investigations into controlled release applications. Full article

Salt efflorescence is always a main barrier for pottery cultural relic conservation. This study presents an innovative two-step process for enhancing the reinforced strength of efflorescence pottery. The first step involves forming a cross-linked mesh structure on the weathered surfaces using ethyl orthosilicate hydrolysate as an organic reinforcement material. In the second step, a two-component inorganic reinforcement material is developed to transform the destructive salt into a filling reinforcement material. The reinforcement pottery was comparatively investigated by XRD, color difference analysis, penetration depth measurements, mechanical strength tests, permeability assessment, and surface morphology characterization. The results demonstrate that the optimized reinforcement material exhibits high water permeability (up to 2.5 cm in penetration depth), stable color variation (ΔE up to 1.44), and excellent mechanical properties (17.01 MPa compressive strength and 2.66 MPa flexural strength). This work presents a promising technique for enhancing the structural interlocking between reinforcement pottery, which is crucial for mitigating dominant salt damage, and suggests an effective strategy that is applicable to the protection of cultural relics. Full article

Organic solvent nanofiltration (OSN) is a promising technology for solute removal from organic media, yet developing membranes with stable separation performance remains challenging. This study presents a solvent-resistant double-crosslinked nanofiltration membrane fabricated via a two-step strategy: preparation of the membrane by the polyion complexion reaction-assisted non-solvent-induced phase inversion (PIC-assisted NIPS) method and then post-crosslinking with hydrothermal treatment followed by quaternization with 1,3,5-tris(bromomethyl)benzene (TBB). To enhance solvent stability, molybdenum sulfide (MoS₂) nanosheets were incorporated into a hydrolyzed polyacrylonitrile (H-PAN) substrate. The H-PAN/MoS₂/PEI base membrane was fabricated by PIC-assisted NIPS with a polyethylenimine (PEI) aqueous solution as the coagulation bath. The membrane subsequently underwent dual crosslinking comprising hydrothermal treatment and 1,3,5-tris(bromomethyl)benzene (TBB)-mediated quaternization crosslinking, ultimately yielding the H-PAN/MoS₂/PEI (Ther.+TBB QCL) composite membrane. These crosslinking procedures reduced the membrane’s separation skin layer thickness from 64 nm (uncrosslinked) to 41 nm. The resultant membrane effectively separated dyes from ethanol, achieving a rejection rate of 97.0 ± 0.9% for anionic dyes (e.g., Congo Red) and a permeance flux of 23.6 ± 0.2 L·m⁻²·h⁻¹·bar⁻¹ at 0.4 MPa. Furthermore, after 30 days of immersion in ethanol at 25 °C, its flux decay rate was markedly lower than that of a non-crosslinked control membrane. The enhanced separation performance and stability are attributed to the thermal crosslinking promoting amide bond formation and the TBB crosslinking introducing quaternary ammonium groups. This double-crosslinking strategy offers a promising approach for preparing high-performance OSN membranes. Full article

Composite solid propellants, which serve as the core energetic materials in aerospace and military propulsion systems, necessitate tailored enhancement of their mechanical properties to ensure operational safety and stability. A critical challenge involves elucidating the interfacial interactions among the multiple propellant components (≥6 components, including the polymer binder HTPB, curing agent IPDI, oxidizer particles AP/Al, bonding agents MAPO/T313, plasticizer DOS, etc.) and their influence on crosslinked network formation. In this study, we propose an integrated computational framework that combines coarse-grained simulations with reactive force fields to investigate these complex interactions at the molecular level. Our approach successfully elucidates the two-step reaction mechanism propagating along the AP interface in multicomponent propellants, comprising interfacial self-polymerization of bonding agents followed by the participation of curing agents in crosslinked network formation. Furthermore, we assess the mechanical performance through tensile simulations, systematically investigating both defect formation near the interface and the influence of key parameters, including the self-polymerization time, HTPB chain length, and IPDI content. Our results indicate that the rational selection of parameters enables the optimization of mechanical properties (e.g., ~20% synchronous improvement in tensile modulus and strength, achieved by selecting a side-chain ratio of 20%, a DOS molar ratio of 2.5%, a MAPO:T313 ratio of 1:2, a self-polymerization MAPO time of 260 ns, etc.). Overall, this study provides molecular-level insights into the structure–property relationships of composite propellants and offers a valuable computational framework for guided formulation optimization in propellant manufacturing. Full article

This study focuses first on the synthesis through an aza-Michael addition reaction of original linear diamine prepolymers and original amine/acrylate thermoset adhesives, and second on their thermal, mechanical and adhesion characterization. The major advantage of the aza-Michael addition reaction is that it takes place at room temperature, without a solvent and without a catalyst. Using the aza-Michael addition reaction, linear secondary diamine prepolymers were first synthesized with a control of the molecular weight, ranging from 867 to 1882 g mol⁻¹. Then, aza-Michael reactions of diamine prepolymers with three different acrylates allowed the synthesis of new amine/acrylate thermoset adhesives. All the thermoset adhesives were characterized by rheology and thermal analysis, leading, once the crosslinking aza-Michael reaction had occurred, to soft thermoset networks with glass transition temperatures ranging from −23 to −8 °C, gel point times ranging from 40 min to 4 h, and a polar component of the surface energy ranging from 3 to 17 mJ m⁻². Functionality of the acrylates directly influences the crosslinking rate, and a decreasing master curve is obtained when reporting crosslinking rate versus gel point time. Crosslinking density is controlled by the diamine prepolymer chain length. In a second step, thermoset adhesives were applied as thin films between two galvanized steel plates, and adhesion properties were evaluated through a lap-shear test. Results showed that the adhesive strength increases as the dynamic viscosity and molecular weight of the diamines prepolymer increases. Increasing the diamines prepolymer chain length results in an increase in strain at break, a decrease in the shear modulus, and a decrease in the maximum lap-shear strength. It is also observed that the adhesive strength decreases when the adhesive film thickness increases. Moreover, thermoset adhesives with high polarity and a surface energy similar to the surface energy of the substrate will favor high adhesion and a better adhesive strength of the assembly. Lastly, the nature of the acrylates and diamines prepolymer chain length allow tuning a wide range of adhesive strength and toughness of these original soft thermoset adhesives. Full article

The development of high-impact denture base formulations that are suitable for digital light processing (DLP) 3D printing is demanding. Indeed, a combination of high flexural strength/modulus and high fracture toughness is required. In this contribution, eight urethane macromonomers (UMs1-8) were synthesized in a one-pot, two-step procedure. Several rigid diols were first reacted with two equivalents of trimethylhexamethylene diisocyanate. The resulting diisocyanates were subsequently end-capped with a free-radically polymerizable monomer bearing a hydroxy group. UMs1-8 were combined with the monofunctional monomer (octahydro-4,7-methano-1H-indenyl)methyl acrylate and a poly(ε-caprolactone)-polydimethylsiloxane-poly(ε-caprolactone) (PCL-PDMS-PCL) triblock copolymer (BCP1) as a toughening agent. The double-bond conversion, glass transition temperature (T_g), and mechanical properties (flexural strength/modulus, fracture toughness) of corresponding light-cured materials were measured (cured in a mold using a light-curing unit). The results showed that the incorporation of BCP1 was highly efficient at significantly increasing the fracture toughness, as long as the obtained networks exhibited a low crosslink density. The structure of the urethane macromonomer (nature of the rigid group in the spacer; nature and number of polymerizable groups) was demonstrated to be crucial to reach the desired properties (balance between flexural strength/modulus and fracture toughness). Amongst the evaluated macromonomers, UM1 and UM2 were particularly promising. By correctly adjusting the BCP1 content, light-cured formulations based on those two urethane dimethacrylates were able to fulfill ISO20795-1:2013 standard requirements regarding high-impact materials. These formulations are therefore suitable for the development of 3D printable high-impact denture bases. Full article

A platform of two-component cross-linked hydrogel (cGEL) based on gelatinous peptides and anhydride-containing cross-linkers (oPNMA, oPDMA) is extended for use in peripheral nerve regeneration. Hybrid composites with bio-/chemical cues for enhanced biophysical and biochemical properties were fabricated by covalently grafting small molecular, heterobifunctional amines including the nerve growth factor mimetic LM11A-31 to the oligomeric cross-linkers prior to hydrogel formation. The cytocompatibility and growth-supportive conditions within the matrix are confirmed for pristine and modified hydrogels using L929 mouse fibroblasts and human adipose-derived stem cells (hASCs). For hASCs, cell behavior depends on the type of cross-linker and integrated amine. In a subsequent step, neonatal rat Schwann cells (SCs) are seeded on pristine and functionalized cGEL to investigate the materials’ capabilities to support SC growth and morphology. Within all formulations, cell viability, adherence, and cell extension are maintained though the cell elongation and orientation vary compared to the two-dimensional control. It is possible to merge adjustable two-component hydrogels with amines as biochemical signals, leading to improved nervous cell proliferation and activity. This indicates the potential of tunable bioactive cGEL as biomaterials in nerve implants, suggesting their use as a foundational component for nerve conduits. Full article

This study presents the development and analysis of hybrid polyurea composite materials. Neat polyurea was reinforced with cellulose nanocrystals (CNCs) and isocyanate-modified CNCs (CNC-ISOs) via a two-step prepolymer process. Introducing CNC considerably increased the mechanical strength and stiffness of the polyurea matrix. The tensile strength increased by up to 16.4%, and the Young modulus improved by approximately 29% compared to the pure polyurea. When CNC was functionalized with isocyanate, the interfacial bonding was further improved, and superior dispersion and load transfer were achieved. At 1.5% CNC-ISO loading, the modulus increased by approximately 128% compared to the unmodified matrix. Comprehensive analyses using FT-IR, XPS, DSC, TGA, DMA, tensile testing, and SEM showed that CNC-ISO films not only achieved higher tensile strength and better thermal stability but also formed a denser polymer network as evidenced by the increased crosslinking density. These findings highlight the importance of tailored nanofiller modification to create advanced polyurea composites with enhanced performance suitable for demanding protective and structural applications. Full article

Tannic acid (TA) possesses antioxidant, anticancer, and antibacterial properties. However, its pH sensitivity, protein cross-linking properties, and susceptibility to oxidation restrict its application. To address these challenges, W/O/W multiple emulsified TA microcapsules were developed using soybean protein isolate (SPI) as the natural wall material emulsifier through a two-step emulsification and spray drying process. The encapsulation efficiency of the obtained TA microcapsules was 87.6%, and TA’s thermal stability was significantly improved. TA microcapsules effectively reduced the acidity and irritability of TA, eliminated protein flocculation, and enhanced biocompatibility. Notably, the cell viability of the TA microcapsule (>94%) was significantly higher than free TA (65.6%). The storage stability test revealed that the microcapsules maintained structural integrity, with a retention rate of 96% after 10 days of storage. In vitro release studies of TA microcapsules demonstrated a sustained-release effect within 24 h. Simulated digestion studies further elucidated the protective effect of microcapsules on TA during gastric digestion. These multi-structured microcapsules based on SPI effectively address the limitations associated with TA utilization and enhance its potential for dual oral/transdermal administration in biomedical and cosmetic applications. Full article

Here, we report the development of a novel bifunctional nanobiocatalyst for a one-pot cascade transformation of carboxymethyl cellulose (CMC) to D-sorbitol. The nanobiocatalyst is based on magnetic nanoparticle aggregates (MNAs) functionalized with chitosan (CS) cross-linked by tripolyphosphate (TPP). It contains two types of catalytic sites: cellulase (Cel, 5 wt.%) and Ru (3 wt.%) nanoparticles (NPs) of 0.7 nm in diameter. To optimize the nanobiocatalyst structure and composition, we first synthesized the biocatalyst, MNA-CSP-Cel (CSP stands for the CS layer cross-linked by TPP), as well as the nanocatalyst, MNA-CSP-Ru, and studied them in the one-step reactions of hydrolysis and hydrogenation, respectively. The data obtained allowed us to optimize the composition and properties of the bifunctional nanobiocatalyst, MNA-CSP-Ru-Cel, and to choose the best reaction conditions for the cascade process. MNA-CSP-Ru-Cel was characterized using transmission electron microscopy (TEM), high-resolution TEM, energy-dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and porosity measurements. The knowledge obtained enabled us to perform a cascade transformation of CMC to D-sorbitol with a yield of 83.2% for 10 h at 70 °C and a hydrogen pressure of 4 MPa. The yield demonstrated in this work is much higher than that reported to date for the same cascade process. Full article

Cartilage damage is common in sports injuries and cartilage-related diseases, such as degenerative joint and rheumatic disorders. Autologous chondrocyte implantation (ACI) is a widely used cell-based therapy for repairing cartilage damage in clinical practice. In this procedure, a patient’s chondrocytes are isolated, cultured in vitro to expand the cell population, and then implanted into the damaged site. However, in vitro expansion of chondrocytes on standard 2D culture surfaces leads to dedifferentiation (loss of the chondrocyte phenotype), and the delivery of detached cells has proven to be ineffective. To overcome these limitations, the matrix-assisted ACI (MACI) procedure was developed. In MACI, matrices such as hydrogels and microspheres are used as cell carriers or scaffolds to deliver expanded chondrocytes, enhancing cell viability and precision delivery. To streamline the two key steps of MACI—cell expansion and delivery—this study aims to investigate various configurations of gelatin-based hydrogels for their potential to support both cell expansion and delivery as a single step. This study evaluated gelatin microspheres (Gel MS), micronized photo-crosslinked GelMA microparticles (GelMA MP), and bulky GelMA hydrogels containing cells (GelMA HG). Cell growth, maintenance of the chondrocyte phenotype, and cartilage extracellular matrix (ECM) production were assessed in pellet cultures for cells grown on/in these carriers, compared with cells cultured on tissue culture-treated polystyrene (TCP). Our results demonstrate that normal human knee articular chondrocytes exhibit robust growth on Gel MS and form aggregates enriched with glycosaminoglycan-rich ECM. Gel MS outperformed both GelMA MP and GelMA HG as a cell carrier by both supporting long-term cell growth with reduced dedifferentiation and precision delivery. Full article

Nanocomposite hydrogels are gaining significant attention for biomedical applications in soft tissue engineering due to the increasing demand for highly flexible and durable soft polymer materials. This research paper focused on investigating and optimizing a procedure for the development of novel nanocomposite hydrogels based on poly(2-hydroxyethyl methacrylate)-co-(2-acrylamido-2-methylpropane sulfonic acid) (HEMA/AMPSA) copolymers. These hydrogels were synthesized through a grafting-through process, where the polymer network was formed using a modified clay crosslinker. The layered double hydroxide (LDH) clay modified with 3-(trimethoxysilyl)propyl methacrylate (ATPM) was synthesized using a novel recipe through a two-step procedure. The nanocomposite hydrogel compositions were optimized to achieve soft hydrogels with high flexibility. The developed materials were analyzed for their mechanical and morphological properties using tensile and compressive tests, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and micro-computed tomography (micro-CT). The swelling behavior, network density, and kinetic diffusion mechanism demonstrated the specific characteristics of the materials. The modified LDH-ATPM was further characterized using Thermogravimetry (TGA), FTIR-ATR and X-ray diffraction (XRD). Biological assessments on human adipose-derived stem cells (hASCs) were essential to evaluate the biocompatibility of the nanocomposite hydrogels and their potential for soft tissue applications. Full article

Due to excellent chemical resistance and impermeability, high-density polyethylene (HDPE) is widely used in petrochemical transportation, product packaging, sports equipment, and marine applications. Yet, with the wide variety of service environments, its mechanical and thermal properties do not meet the demand. In the present study, a compounding cross-linker comprising di-tert-butyl peroxide (DTBP) and triallyl isocyanurate (TAIC) is employed by combining with a two-step preparation process. High-quality cross-linking reactions are achieved for HDPE. In this study, the cross-linking of DTBP is first examined separately. A peak cross-linking degree of 74.7% is achieved, and there is a large improvement in thermal resistance and mechanical properties. Subsequently, the composite cross-linking system of DTBP and TAIC is investigated. The peak cross-linking degree is 82.1% (10% increase compared to DTBP). The peak heat deformation temperature is 80.1 °C (22% increase compared to DTBP). The peak impact strength is 104.73 kJ/m² (207% increase compared to neat HDPE). The flexural strength is 33.6 MPa (22% increase compared to neat HDPE). The results show that this cross-linking system further improves the cross-linking degree, heat resistance, and mechanical properties of HDPE, indicating its potential application in engineering materials for high performance. Full article

The objective of this study is to evaluate the degradation of end-of-life BWRO membranes sourced from a factory in France by analyzing their water permeability, roughness, and chemical composition in order to diagnose the level of degradation incurred during their first life cycle in water softening. Following this, two new applications for the end-of-life BWRO membranes were investigated: (i) as ultrafiltration membranes (UF) for domestic effluent treatment and (ii) as cation exchange membranes (CEM) for use in fungal microbial fuel cells (FMFC). The UF membrane was renovated with an acetic acid treatment and, subsequently, used for domestic effluent filtration. The cation exchange membrane was developed in two steps: (i) chlorine treatment and (ii) the deposition of an Amer Sil layer, a functional coating formed by an interpenetrating polymer network (IPN) made of sulfonated polyether sulfone (S-PES) in a cross-linked matrix of acrylic acid and divinylbenzene. Full article

This project intends to develop restorative dental nanomaterial composites that are light-curable and show minimal shrinkage. Such nanocomposites are improved via employing 2,2-bis[4(2-hydroxy-3-methacryloylpropyloxy) phenyl] propane (Bis-GMA) with the unsaturated monomers bisphenol A dimethacrylate, N,N-dimethylacetamide (DMA), ethylene glycol (EG), and methacrylic acid (MAA) and loading them with SiO₂, ZrO₂, or hydroxyapatite (HA) as nanofillers of 10–30 nm. The first step was to create and characterize these novel dental materials. 1,6-hexanediol methacrylate (HDOMA) was used as a cross-linking agent. The composites based on Bis-GMA and HDOMA with a mass ratio of 40/20 were loaded with 2.5, 5.0, 7.5, 10.0, 12.5, and 15.0 wt.% of the fillers mentioned above. Photopolymerization was induced by a system of photoinitiation based on Camphorquinone/2- (Diethyl amino) ethyl acrylate (CQ/DMAEMA). The nanofillers were treated with 3-(methacryloyloxy) propyltrimethoxysilane (MPTMS) at a ratio of 1.5, 2.5, as well as 3.5%wt. compared to the filler) and a silane coupling agent to increase bonding between the phases and reduce the tendency of agglomerations. SEM images displayed the adhesion between the matrix and the three functionalized nanofillers. FTIR was used to prove the functionalization of the nanofillers by silanization with MPTMS. According to the polymer matrix, two different series of dental nanocomposites were obtained. The compressive strength of dental nanocomposites treated with 2.5 wt.% MPTMS was considerably more significant than those treated with 1.5 and 3.5%wt. MPTMS. Compressive strength (CS) and volumetric shrinkage (VS) were examined as examples of physicochemical properties. This improved nanocomposite was tested for its suitability as a dental restorative material and found to have low shrinkage and high strength. Full article