Cross-linking Method Research Articles

A transparent, anti‐blue‐light, and high strength nylon/nickel phosphate oligomer nanocomposite formed via intermolecular hydrogen bond crosslinking

AbstractPolymer/transition metal inorganic salts nanocomposites are promising engineering materials in automotive, electronics, aerospace and smart wearables fields. However, the interfacial incompatibility always causes agglomeration and phase separation, constraining their further application. Inspired by inorganic oligomers' polymerization, nylon/nickel phosphate oligomer (NPO) nanocomposite (ENCC) was prepared via hydrogen bond crosslinking method. Due to the formation of hydrogen bonds between PO43− end groups of NPO with an average diameter of 6.5 ± 1.2 nm and NH groups on the nylon molecular chain, the phase compatibility is greatly improved. Hence, NPO was uniformly nano‐dispersed and had no obvious agglomerate in ENCC, inducing an invisible phase interface at nano‐micro scale. Nylon/nickel phosphate oligomer showed an excellent reinforcing effect on nylon, the tensile strength and elongation of ENCC reached 28 ± 0.8 MPa and 585 ± 26% at a high loading of 20 wt%, increased by 155% and 92%, compared with pure matrix, respectively. Furthermore, ENCC was still optically transparent and had excellent anti‐blue‐light performance (up to 96.6%).Highlights Novel inorganic/nylon composite prepared by hydrogen bond crosslinking method. Phase separation and aggregation problems were solved remarkably. Inorganic metal phosphate dispersed with a diameter of 6.5 ± 1.2 nm. The composite was still transparent at 20 wt% loading of metal phosphate. Tensile strength and elongation increased by 155% and 92%, respectively.

Natural Regenerative Hydrogels for Wound Healing.

Regenerative hydrogels from natural polymers have come forth as auspicious materials for use in regenerative medicine, with interest attributed to their intrinsic biodegradability, biocompatibility, and ability to reassemble the extracellular matrix. This review covers the latest advances in regenerative hydrogels used for wound healing, focusing on their chemical composition, cross-linking mechanisms, and functional properties. Key carbohydrate polymers, including alginate, chitosan, hyaluronic acid, and polysaccharide gums, including agarose, carrageenan, and xanthan gum, are discussed in terms of their sources, chemical structures and specific properties suitable for regenerative applications. The review further explores the categorization of hydrogels based on ionic charge, response to physiological stimuli (i.e., pH, temperature) and particularized roles in wound tissue self-healing. Various methods of cross-linking used to enhance the mechanical and biological performance of these hydrogels are also examined. By highlighting recent innovations and ongoing challenges, this article intends to give a detailed understanding of natural hydrogels and their potential to revolutionize regenerative medicine and improve patient healing outcomes.

Study of glutaraldehyde-treated crosslinking protocols for placental decellularized matrix sponges

Extracellular matrix sponge plays a positive role in the wound healing process, but requires proper structural strength and biological properties. In order to solve the problem of lyophilized dissolution of placenta-derived sponge, glutaraldehyde was selected for use in the lyophilized crosslinking process to improve the necessary mechanical properties of the placental decellularization matrix sponge. In this work, the effects of three cross-linking methods of glutaraldehyde (Fumigation/Slurry/Soak) on the physical and biological characteristics of lyophilised sponges derived from placental acellular matrix was investigated. The results revealed that the sponges prepared by all three cross-linking methods exhibited excellent blood coagulation ability and stability. The fumigation cross-linked sponges had good mechanical properties of soft and elastic, and safe cytotoxicity, which were more compatible with the requirements of wound dressing. The slurry cross-linking process was uneven due to the stacked matrix materials, resulting in obvious cracks and easy to break when stretching. The soak crosslinking can obtain a higher degree of crosslinking, which leads to the poor antibacterial performance and the harder sponge scaffold with larger elastic modulus and smaller tensile ratio. In general, fumigation cross-linking is more suitable for the preparation of acellular sponge derived from placenta materials which can maintain basic mechanical properties and biological validity.

Mussel-Inspired Injectable Adhesive Hydrogels for Biomedical Applications.

The impressive adhesive capacity of marine mussels has inspired various fascinating designs in biomedical fields. Mussel-inspired injectable adhesive hydrogels, as a type of promising mussel-inspired material, have attracted much attention due to their minimally invasive property and desirable functions provided by mussel-inspired components. In recent decades, various mussel-inspired injectable adhesive hydrogels have been designed and widely applied in numerous biomedical fields. The rational incorporation of mussel-inspired catechol groups endows the injectable hydrogels with the potential to exhibit many properties, including tissue adhesiveness and self-healing, antimicrobial, and antioxidant capabilities, broadening the applications of injectable hydrogels in biomedical fields. In this review, we first give a brief introduction to the adhesion mechanism of mussels and the characteristics of injectable hydrogels. Further, the typical design strategies of mussel-inspired injectable adhesive hydrogels are summarized. The methodologies for integrating catechol groups into polymers and the crosslinking methods of mussel-inspired hydrogels are discussed in this section. In addition, we systematically overview recent mussel-inspired injectable adhesive hydrogels for biomedical applications, with a focus on how the unique properties of these hydrogels benefit their applications in these fields. The challenges and perspectives of mussel-inspired injectable hydrogels are discussed in the last section. This review may provide new inspiration for the design of novel bioinspired injectable hydrogels and facilitate their application in various biomedical fields.

Bovine Placentome-Derived Extracellular Matrix: A Sustainable 3D Scaffold for Cultivated Meat.

Cultivated meat, an advancement in cellular agriculture, holds promise in addressing environmental, ethical, and health challenges associated with traditional meat production. Utilizing tissue engineering principles, cultivated meat production employs biomaterials and technologies to create cell-based structures by introducing cells into a biocompatible scaffold, mimicking tissue organization. Among the cell sources used for producing muscle-like tissue for cultivated meats, primary adult stem cells like muscle satellite cells exhibit robust capabilities for proliferation and differentiation into myocytes, presenting a promising avenue for cultivated meat production. Evolutionarily optimized for growth in a 3D microenvironment, these cells benefit from the biochemical and biophysical cues provided by the extracellular matrix (ECM), regulating cell organization, interactions, and behavior. While plant protein-based scaffolds have been explored for their utilization for cultivated meat, they lack the biological cues for animal cells unless functionalized. Conversely, a decellularized bovine placental tissue ECM, processed from discarded birth tissue, achieves the biological functionalities of animal tissue ECM without harming animals. In this study, collagen and total ECM were prepared from decellularized bovine placental tissues. The collagen content was determined to be approximately 70% and 40% in isolated collagen and ECM, respectively. The resulting porous scaffolds, crosslinked through a dehydrothermal (DHT) crosslinking method without chemical crosslinking agents, supported the growth of bovine myoblasts. ECM scaffolds exhibited superior compatibility and stability compared to collagen scaffolds. In an attempt to make cultivate meat constructs, bovine myoblasts were cultured in steak-shaped ECM scaffolds for about 50 days. The resulting construct not only resembled muscle tissues but also displayed high cellularity with indications of myogenic differentiation. Furthermore, the meat constructs were cookable and able to sustain the grilling/frying. Our study is the first to utilize a unique bovine placentome-derived ECM scaffold to create a muscle tissue-like meat construct, demonstrating a promising and sustainable option for cultivated meat production.

Pneumatic extrusion bioprinting-based high throughput fabrication of a melanoma 3D cell culture model for anti-cancer drug screening

The high incidence of malignant melanoma highlights the need forin vitromodels that accurately represent the tumour microenvironment, enabling developments in melanoma therapy and drug screening. Despite several advancements in 3D cell culture models, appropriate melanoma models for evaluating drug efficacy are still in high demand. The 3D pneumatic extrusion-based bioprinting technology offers numerous benefits, including the ability to achieve high-throughput capabilities. However, there is a lack of research that combines pneumatic extrusion-based bioprinting with analytical assays to enable efficient drug screening in 3D melanoma models. To address this gap, this study developed a simple and highly reproducible approach to fabricate a 3D A375 melanoma cell culture model using the pneumatic extrusion-based bioprinting technology. To optimise this method, the bioprinting parameters for producing 3D cell cultures in a 96-well plate were adjusted to improve reproducibility while maintaining the desired droplet size and a cell viability of 92.13 ± 6.02%. The cross-linking method was optimised by evaluating cell viability and proliferation of the 3D bioprinted cells in three different concentrations of calcium chloride. The lower concentration of 50 mM resulted in higher cell viability and increased cell proliferation after 9 d of incubation. The A375 cells exhibited a steadier proliferation rate in the 3D bioprinted cell cultures, and tended to aggregate into spheroids, whereas the 2D cell cultures generally formed monolayered cell sheets. In addition, we evaluated the drug responses of four different anti-cancer drugs on the A375 cells in both the 2D and 3D cell cultures. The 3D cell cultures exhibited higher levels of drug resistance in all four tested anti-cancer drugs. This method presents a simple and cost-effective method of producing and analysing 3D cell culture models that do not add additional complexity to current assays and shows considerable potential for advancing 3D cell culture models' drug efficacy evaluations.

Huge improved gas separation performance of carbon molecular sieve membrane by forming a double crosslinked polyimide precursor

A vital issue in searching for advanced gas separation membranes is understanding the precursor structure-gas separation properties of carbon molecular sieve (CMS) membranes. Here, we reported two crosslinked polyimides and used as CMS precursors, in which, the DCPI-4 is a double cross-linkable polyimide with 4 % triptycene triamine as a crosslinker (Type I) and COOH group that can be crosslinked at 350 °C by decarboxylation (Type II), whereas the DCPI-0 with COOH (Type II). After pyrolysis at 550 °C, the DCPI-4-CMS showed a higher SBET (812 vs 713 m2g-1), larger ultra-microporosity ratio (26.6 % vs 17.8 %), larger d-spacing (4.08 vs 3.94 Å), less graphitization (sp3/sp2 of 0.156 vs 0.118), 5.5 times higher CO2 permeability (7573 vs 1391 Barrer) and same CO2/CH4 selectivity (∼62) than DCPI-0-CMS. We consider this is due to the type I crosslinking enhances the rigidity of the polyimide backbone, and inhibits the collapse of micropores during the carbonization, which causes improved ultra-microporosity and ultra-micropore ratio that both enhances the gas diffusion and solubility coefficient as well activation energy difference of gas pairs. Conclusively, this double crosslinking method provides a good perspective for achieving CMS membranes with excellent gas separation performance.

Enhanced CO2 Capture Potential of Chitosan-Based Composite Beads by Adding Activated Carbon from Coffee Grounds and Crosslinking with Epichlorohydrin.

Carbon dioxide (CO2) capture has been identified as a potential technology for reducing the anthropic emissions of greenhouse gases, particularly in post-combustion processes. The development of adsorbents for carbon capture and storage is expanding at a rapid rate. This article presents a novel sustainable synthesis method for the production of chitosan/activated carbon CO2 adsorbents. Chitosan is a biopolymer that is naturally abundant and contains amino groups (-NH2), which are required for the selective adsorption of CO2. Spent coffee grounds have been considered as a potential feedstock for the synthesis of activated coffee grounds through carbonization and chemical activation. The chitosan/activated coffee ground composite microspheres were created using the emulsion cross-linking method with epichlorohydrin. The effects of the amount of chitosan (15, 20, and 25 g), activated coffee ground (10, 20, 30, and 40%w/w), and epichlorohydrin (2, 3, 4, 5, 6, 7 and 8 g) were examined. The CO2 capture potential of the composite beads is superior to that of the neat biopolymer beads. The CO2 adsorbed of synthesized materials at a standard temperature and pressure is improved by increasing the quantity of activated coffee ground and epichlorohydrin. These findings suggest that the novel composite bead has the potential to be applied in CO2 separation applications.

Preparation of chitosan resin by two-step crosslinking method and its adsorption for palladium in wastewater

To preserve the activity of amine groups on chitosan, chitosan resin (CR) was synthesized using the reversed-phase suspension two-step crosslinking method for the adsorption of palladium from wastewater. The effects of varying the amounts of chitosan, liquid paraffin, ethyl acetate, formaldehyde solution, and epichlorohydrin on the adsorption capacity of CR were investigated using both single-factor experiments and response surface methodology. The preparation conditions for the chitosan resin were optimized, and its adsorption properties were systematically evaluated. The results indicated that CR exhibited a high saturated adsorption capacity for palladium, reaching 195.22 mg·g−1. The adsorption kinetics followed the pseudo-second-order model, while the adsorption isotherms were well described by the Sips model. Thermodynamic analysis demonstrated that the adsorption process was spontaneous and endothermic. Furthermore, CR maintained exceptional stability, with a palladium removal efficiency exceeding 99.8 % even after eight adsorption-desorption cycles. The primary adsorption mechanism is attributed to the interaction between palladium ions and the protonated amino groups of the chitosan resin.

MOF-801 enabled rapid-cycling atmospheric water harvester with vertically aligned photothermal channel

Sorption-based atmospheric water harvesting (SAWH) with metal–organic frameworks (MOFs) offer a promising solution to freshwater scarcity in arid regions. However, given the powder nature of MOFs, scaling-up such a concept with industrially favorable monolithic MOFs in bulky sizes remains challenging. In this study, a pore vertically aligned nanocomposite sorbent where MOF-801 is anchored at the polymeric structure surface was prepared via Fe3+-induced crosslinking and directional freezing methods. The continuous vertically aligned hierarchical pores not only offer sufficient sites for MOF-801 loading but also provide rapid moisture transport channels, as well as high solar-thermal conversion efficiency, resulting in a rapid ab/desorption duration of 2 h (including an absorption process for 1 h and a desorption process for 1 h under 1 sun irradiation) and multicycle daily water production of 1.40 L kg−1 at low RH of 20 % and 5.57 L kg−1 at higher RH of 80 %, respectively, which is outperformed most of the state-of-the-art MOFs based SAWH materials. This work provides a simple and effective way to shorten MOF-801 ab/desorption duration, which has great means for designing of high-performance solar-driven water harvesting materials.

Development of Pentablock Copolymer Membranes for a Sodium Polysulfide Hybrid Redox Flow Battery

Long duration energy storage devices, such as redox flow batteries (RFBs), are critical for enabling the widespread adoption of renewable energy sources such as wind and solar on the electric grid. Non-aqueous RFBs (NARFBs) have emerged as a possible alternative to aqueous RFBs (e.g., all-vanadium and Zn/Br systems), as they have the potential to use supporting electrolytes with wide operating voltage windows (>3 V) and a variety of redox couples. One NARFB of interest is a hybrid RFB that utilizes an alkali metal anode, such as sodium, and a polysulfide catholyte. However, the realization of a hybrid NARFB for long duration energy storage requires the development of new membranes with robust mechanical properties, good (electro)chemical stability, high ionic conductivity, and low polysulfide permeability. In this work, we have utilized a cation exchange pentablock copolymer membrane with sodium sulfonate and sodium trifluoromethanesulfonimide (TFSI) functionalities. We studied various crosslinking methods with the goal of reducing electrolyte uptake and polysulfide crossover of the membrane, while maintaining high ion transport. One lightly crosslinked membrane exhibits a 40% reduction in electrolyte uptake compared to the uncrosslinked membrane, but at the expense of a reduction in ionic conductivity from 2.5 x 10-4 S/cm to 4.2 x 10-5 S/cm at 20 °C. Our continued efforts in developing techniques to improve membrane properties will also be discussed.

A dual crosslinking strategy to tailor rheological properties of gelatin methacryloyl

3D bioprinting is an emerging technology that enables the fabrication of three-dimensional organised cellular constructs. One of the major challenges in 3D bioprinting is to develop a material to meet the harsh requirements (cell-compatibility, printability, structural stability post-printing and bio-functionality to regulate cell behaviours) suitable for printing. Gelatin methacryloyl (GelMA) has recently emerged as an attractive biomaterial in tissue engineering because it satisfies the requirements of bio-functionality and mechanical tunability. However, poor rheological property such as low viscosity at body temperature inhibits its application in 3D bioprinting. In this work, an enzymatic crosslinking method triggered by Ca2+-independent microbial transglutaminase (MTGase) was introduced to catalyse isopeptide bonds formation between chains of GelMA, which could improve its rheological behaviours, specifically its viscosity. By combining enzymatic crosslinking and photo crosslinking, it is possible to tune the solution viscosity and quickly stabilize the gelatin macromolecules at the same time. The results showed that the enzymatic crosslinking can increase the solution viscosity. Subsequent photo crosslinking could aid in fast stabilization of the structure and make handling easy.

EFFECT OF CHITOSAN CONCENTRATION ON PHYSICAL CHARACTERISTICS OF EXTRACT ETHANOLIC OF BAY LEAF (Syzygium polyanthum) NANOPARTICLE PREPARED BY CROSS-LINKING METHODS

Chitosan is a natural cationic polysaccharide that could form bonds with negatively charged polyanions like sodium tripolyphosphate (STPP) as a crosslinker. One of the important factors to develop nanoparticles is the concentration of polymer. The increased polymer concentration will increase the viscosity of the solution formed, and the size of the nanoparticles created will increase. However, if the amount of polymer is too small, the particles formed are smaller, and aggregation could be formed. In this study, the ethanolic extract of bay leaf (Syzygium polyanthum) was used as a drug that has a potent anti-dyslipidemia effect by lowering cholesterol and triglyceride levels. Studies on the ethanolic extract of a bay leaf as an anti-dyslipidemia are still limited. The objective of this research was an investigate effect of the chitosan concentration used 0.6 mg/ml (F1); 1mg/ml (F2); and 1.4 mg/ml (F3) on the physical characteristics of ethanolic extract of bay leaf (Syzygium polyanthum) nanoparticles (NSPs) prepared by cross-linking methods. The result of particle size evaluation showed that the particle size was 665.1 nm ± 14.71 (F1); 180.1 nm ± 0.5; and 221.35 nm ± 1.91 (F3), while the polydispersity index F1, F2, and F3 were 0.773 ± 0.152; 0.220 ± 0.016; and 0.212 ± 0.024 respectively. The results of this study found F2 was the most optimal chitosan concentration with particle size under 200 nm, and polydispersity index under 0.5 with positive ζ-potential value. In conclusion, chitosan concentration showed has an effect on the physical characteristics of the nanoparticles.

Design of Collagen and Gelatin-based Electrospun Fibers for Biomedical Purposes: An Overview.

Collagen and gelatin are essential natural biopolymers commonly utilized in biomaterials and tissue engineering because of their excellent physicochemical and biocompatibility properties. They can be used either in combination with other biomacromolecules or particles or even exclusively for the enhancement of bone regeneration or for the development of biomimetic scaffolds. Collagen or gelatin derivatives can be transformed into nanofibrous materials with porous micro- or nanostructures and superior mechanical properties and biocompatibility using electrospinning technology. Specific attention was recently paid to electrospun mats of such biopolymers, due to their high ratio of surface area to volume, as well as their biocompatibility, biodegradability, and low immunogenicity. The fiber mats with submicro- and nanometer scale can replicate the extracellular matrix structure of human tissues and organs, making them highly suitable for use in tissue engineering due to their exceptional bioaffinity. The drawbacks may include rapid degradation and complete dissolution in aqueous media. The use of gelatin/collagen electrospun nanofibers in this form is thus greatly restricted for biomedicine. Therefore, the cross-linking of these fibers is necessary for controlling their aqueous solubility. This led to enhanced biological characteristics of the fibers, rendering them excellent options for various biomedical uses. The objective of this review is to highlight the key research related to the electrospinning of collagen and gelatin, as well as their applications in the biomedical field. The review features a detailed examination of the electrospinning fiber mats, showcasing their varying structures and performances resulting from diverse solvents, electrospinning processes, and cross-linking methods. Judiciously selected examples from literature will be presented to demonstrate major advantages of such biofibers. The current developments and difficulties in this area of research are also being addressed.

Rational Design of a Multifunctional Hydrogel Trap for Water and Fertilizer Capture: A Review.

Water scarcity and land infertility pose significant challenges to agricultural development, particularly in arid and semiarid regions. Improving soil-water-retention capacity and fertilizer utilization efficiency through the application of soil additives has become a pivotal approach in agricultural practices. Hydrogels exhibit exceptional water absorption and fertilizer retention capabilities, making them extensively utilized in the fields of agriculture, forestry, and desert control. Currently, most reviews primarily focus on the raw materials, classification, synthesis methods, and application prospects of hydrogels, with limited attention given to strategies for enhancing water-retention performance, mechanisms underlying fertilizer absorption, and environmental risks. This review covers the commonly used cross-linking methods in hydrogel synthesis and the structure-activity relationship between hydrogels and water as well as fertilizer. Additionally, a thorough analysis of the ecological benefits and risks associated with hydrogels is presented. Finally, future prospects and challenges are delineated from the perspectives of material design and engineering applications.

Structure and thermal properties of acrylic copolymer gels: effect of composition and cross-linking method

Two approaches to the synthesis of hydrogels based on polyacrylamide (pAAm) with copolymers were compared in the paper—traditional chemical cross-linking and physical cross-linking with montmorillonite (MMT). The main aim of the work was to find an adequate replacement of the chemical toxic cross-linking agent MBAAm (N,N'-methylene-bis-acrylamide) by using non-toxic—natural clay MMT for synthesis of pAAm gels, which are planned to be used as soil conditioners. A series of hydrogels based on acrylic monomers (acrylamide (AAm), acrylonitrile (AN), acrylic acid (AA)) physically cross–linked by MMT and chemically cross-linked were synthesized. For the synthesized gels, the influence of the synthesis method on the formation of the structure and the mechanism of thermal destruction in the presence of air was analyzed using a set of physicochemical methods: FTIR, XRD, SEM, DSC and TG/DTG. According to FTIR and XRD data, pAAm-MMT and pAAm-AN-MMT samples formed an intercalated/exfoliated structure, whereas pAAm-AA-MMT had an intercalated structure. The endothermic reaction of decomposition of xerogels based on acrylic polymers with and without MMT was observed using DSC and derivative thermogravimetry analyses, coupled with measurement of FTIR spectra of volatile products of thermolysis. All studied composites were relatively thermoresistant, which had three distinct regions of phase transitions and their thermal decomposition occurred at a temperature range 310–465 °C.Graphical

Fabrication of a reusable Ti3C2Tx MXene/ZnO@zinc alginate hydrogel for highly efficient and selective phosphate removal

Nano-Zinc oxide (ZnO) shows great potential for phosphate adsorption, but its tendencies to aggregate and lack of selectivity significantly impact adsorption efficiency. The synthesis of Ti3C2Tx MXene/ZnO complexes efficiently disperses ZnO, thereby enhancing selectivity, while encountering challenges in recovery. In this study, Ti3C2Tx MXene/ZnO-embedded zinc crosslinked alginate hydrogel beads (MXZA) were synthesized by solution-phase and ionic cross-linking methods as a highly efficient, selective, and reusable phosphate adsorbent. MXZA exhibited a maximum adsorption capacity of up to 86.67 mg/g of phosphate, and showed excellent adsorption selectivity in complex solutions (e.g., Cl-, NO3–, and SO42-). In short, the MXZA gel adsorbent has a wide application perspective in the effective and selective removal of phosphate from wastewater.

Empowering PLA Bioplastics: Elevating applications horizon through groundbreaking Eco-Innovative Fibrillation, chain Extension, and crosslinking techniques

This comprehensive study introduces pioneering techniques in the toughening of polylactic acid (PLA) by incorporating thermoplastic polyurethane (TPU) nanofibrils, leveraging two distinct crosslinking methods to significantly enhance the material’s mechanical performance. Method 1 employs a silane/moisture crosslinking process, whereas Method 2 utilizes a tailored diisocyanate crosslinking approach, offering a more environmentally sustainable alternative. Molecular structural analysis was performed extensively by using X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (1H NMR), gel permeation chromatography (GPC), rheological assessments, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). Method 2 not only preserves TPU nanofibrils but also elevates the mechanical properties of PLA-TPU composites beyond the capabilities of Method 1. Notably, by leveraging the simultaneous crosslinking of TPU and chain extension of PLA with the tailored diisocyanate approach, we enhance PLA’s mechanical properties and energy absorption capabilities. These advancements are achieved without a high rubber content, which typically compromises strength/stiffness, thermomechanical stability, crystallization, and transparency of PLA. The resulting composites prepared via Method 2 display remarkable increases in tensile toughness, ranging from 30-60 MPa, and impact strength, achieving a span of 60–140 J/m. This is primarily due to the occurrence of a brittle-to-ductile transition (BDT) at only 3 wt% nanofibril TPU content while maintaining a high PLA modulus of 3 GPa. This critical balance between chain-extending and crosslinking reactions ensures the maintenance of PLA’s inherent strength/stiffness, crystallization, and optical clarity. The research presented here marks a significant shift in the development of tougher, more thermally stable, transparent, and sustainable polymer blends and composites. Method 2, with its tailored fiber size reduction (90–280 nm), and environmental consciousness, broadens the horizon of PLA’s applications.

Dual-Temperature/pH-Sensitive Hydrogels with Excellent Strength and Toughness Crosslinked Using Three Crosslinking Methods.

Hydrogels are widely used as excellent drug carriers in the field of biomedicine. However, their application in medicine is limited by their poor mechanical properties and softness. To improve the mechanical properties of hydrogels, a novel triple-network amphiphilic hydrogel with three overlapping crosslinking methods using a one-pot free-radical polymerization was synthesized in this study. Temperature-sensitive and pH-sensitive monomers were incorporated into the hydrogel to confer stimulus responsiveness, making the hydrogel stimuli-responsive. The successful synthesis of the hydrogel was confirmed using techniques, such as proton nuclear magnetic resonance spectroscopy (1H NMR), Fourier-transform infrared spectroscopy (FT-IR), and X-ray diffraction (XRD). In order to compare and analyze the properties of physically crosslinked hydrogels, physically-chemically double-crosslinked hydrogels, and physically-chemically clicked triple-crosslinked hydrogels, various tests were conducted on the gels' morphology, swelling behavior, thermal stability, mechanical properties, and drug loading capacity. The results indicate that the triple-crosslinked hydrogel maintains low swelling, high mechanical strength, and good thermal stability while not significantly compromising its drug delivery capability.

Immobilization of novel bifunctional polymer with amide and amidoxime groups in biochar-chitosan composite gels for enhancing uranium(VI) uptake

This work synthesized poly ethanolamine amidoxime modified winter melon and chitosan-derived biochar (PEA-CTS@WBC) using chemical crosslinking method for uranium(VI) removal. The factors influencing uranium(VI) adsorption by PEA-CTS@WBC, including pH, adsorbent dosage, time, temperature, and initial U(VI) concentration were explored. The material’s performance was characterized, and the underlying mechanism of U(VI) removal was analyzed using various techniques. The characterization results indicated that the PEA-CTS@WBC took on a membrane shape with numerous pores and wrinkles distributed on the surface, providing more active sites that can effectively promote the complexation and adsorption of U(VI). The results demonstrated that PEA-CTS@WBC effectively removed U(VI), achieving a maximum adsorption capacity of 485.89 mg/g at the pH of 5.0. The process suggested a dominant role for chemical adsorption. The Freundlich isotherm model demonstrated a high degree of alignment with the observed adsorption behavior, indicating a predominantly multilayer adsorption process. Thermodynamic studies indicated that adsorption was a spontaneous endothermic process. The XPS analysis demonstrated that the adsorption process was primarily due to the formation of stable complexes with NH3+-C(O), N–C, C–N, C=C, O–H and C=O. This research showed that the introduction of amide and amidoxime groups significantly improved the adsorption effect of biochar-chitosan gels on U(VI). PEA-CTS@WBC had a high selective adsorption characteristics and good reusability for U(VI) in aqueous solutions. PEA-CTS@WBC was an economical, efficient and stable composite material. These findings provided a theoretical basis for the treatment of wastewater contaminated with U(VI).