Degree Of Crosslinking Research Articles

New fibrous carboxyl cation exchangers for sorption cations of heavy and non-ferrous metals from water

New fibrous carboxyl cation exchangers FIBAN were synthesized by the method of graft copolymerization to polypropylene staple fibers of acrylic acid and various bifunctional comonomers (divinylbenzene – DVB, ethyleneglycoldimethacrylate – EGDM, methylene-bis-acrylamide – MBAA). Sorption properties of the fibers towards cations of heavy and non-ferrous metals (Cо2+, Ni2+, Zn2+, Cd2+, Cu2+ и Pb2+) were studied on the model solutions in the dynamic regime. The dynamic activity of the crosslinked sorbents towards Cu2+ and Pb2+ ions is higher compared to fibrous analogues FIBAN Х-1, FIBAN Х-2, FIBAN К-6М, FIBAN К-5, VION КN-1. The best sorbent for lead ions between the crosslinked fibers is the fiber with EGDM. The fiber with MBAA has a higher affinity towards the cations of Ni2+, Zn2+, Cd2+ and Cа2+, which increases with the increasing of the degree of crosslinking by MBAA. Studying the fibers by the methods of Fourier-transform IR-spectroscopy, scanning electron microscopy, analyzing of the chemical oxygen demand in water extracts and determination of the equivalent moisture capacity coefficient coefficient demonstrated that the crosslinking by MBAA provides a stable structure of the sorbent. The high stability of the crosslinked structure combined with the high ion exchange capacity near 7 mEq/g and dynamic activity towards the cations of Pb2+, Zn2+, Cd2+ и Cа2+ makes the fibrous carboxyl sorbent with MBAA safe and perspective for drinking water purification.

Controlled Release Simvastatine from Molecularly Imprinted Cryogel Membranes

AbstractIn this study, poly(2‐hydroxyethyl methacrylate‐N‐methacryloyl‐L‐tryptophan methyl ester) cryogel membranes were synthesized in different concentrations by using molecular imprinting technique, for controlled release of simvastatin. The cryogel membranes were prepared in various compositions and thus the releases of cryogels containing 0.5, 0.75 and 1 mg hydrophilic simvstatin were compared. The chemical and morphological properties of the poly(HEMA‐MATrp) cryogel membranes were evaluated through a series of characterization techniques. The membranes were subjected to swelling tests to assess their ability to absorb water and their degree of crosslinking. Fourier‐transform infrared spectroscopy was applied to determine the functional groups present in the cryogel matrix and to evaluate the degree of chemical modification that occurred during synthesis. Additionally, scanning electron microscopy was employed to visualize the cryogel at high resolution, providing insights into the pore structure and overall architecture of the matrix. Then, cryogel membranes were evaluated for cell proliferation abilities by 3‐(4,5‐dimethyl/thiazol‐2‐yl) 2,5‐diphenyltetra zolium bromide thiazolyl blue (MTT) assay for cell viability. The prepared cryogel membranes have a diameter and thickness of about 10 mm and 1.0 mm, respectively. The increasing attention towards the use of cryogel membranes in tissue‐engineering has resulted in demonstrating the dependency of release profiles of simvastatin cryogel membranes on their composition.

Elution behavior of carbohydrates using core-shell ion-exchange resin St-60 with different numbers of methylene groups in the porous shell and a constant cross-linking degree of 55%

Elution behavior of carbohydrates using core-shell ion-exchange resin St-60 with different numbers of methylene groups in the porous shell and a constant cross-linking degree of 55%

Low swelling and high mechanical strength organosilane hybrid polydivinylbenzene microspheres for hydrophilic interaction chromatography applications.

In this work, monodisperse organosilane hybrid polymer microspheres with a particle size of about 5µm were synthesized using seed swelling polymerization. The organosilicon reagent methacryloxypropyltrimethoxysilane was introduced into the polymer framework as a copolymerization monomer, and the crosslinking degree of the microspheres was improved by the hydrolysis-condensation reaction of siloxanes. The synthesized hybrid microspheres have good mechanical strength as well as low swelling, with swelling propensity values of 0.167 and 0.348 in methanol and acetonitrile, respectively. Hybrid microspheres modified with cysteine have a hydrophilic interaction chromatography/reversed-phase liquid chromatography mixed-mode retention mechanism. Compared to the commercial cysteine-modified silica column, the synthesized stationary phase has higher separation selectivity for partially acidic or basic samples and better basic resistance for use under high pH mobile phase conditions (at least 10).

Constructing multiple bonding mechanisms with a novel lignin-activated modified polymer core for the fabrication of strong, water-resistant, and mildew-resistant adhesives

Biobased adhesives play a pivotal role in the development of eco-friendly wood products, and phytogenic protein as a biobased material preparation adhesive has the advantages of sustainable development and green environmental protection. Current researches focus and challenge lie in developing phytogenic protein adhesives that do not emit formaldehyde and possess high water-resistant bonding strength and anti-mold properties through the use of biobased cross-linkers instead of chemical cross-linkers. In this study, lignin, a natural polymer material, was used as raw material to fabricate a novel crosslinker, and a cross-linking network structure was constructed with lignin as the cross-linking core and multiple bonding effects of hydrogen and chemical bonds. In addition, lignin-based crosslinker was prepared to replace the chemical crosslinker while successfully activating lignin to improve the crosslinking degree between lignin and the protein matrix. This study addressed environmental pollution and cost issues associated with the extensive use of chemical cross-linkers in phytogenic protein adhesives. The water-resistant bonding strength of the prepared phytogenic protein adhesive reached 1.21 MPa, and the mechanical properties of the prepared phytogenic protein adhesive were increased by 188 % compared with the ordinary phytogenic protein adhesive and exhibited effective anti-mold properties. This research provided a novel approach for creating sustainable, environmentally friendly adhesives and held significant implications for producing industrial wood-based panels.

Preliminary Study on Polymerization between Hemoglobin and Enzymes during the Preparation of PolyHb-SOD-CAT-CA.

The objective of this study was to explore the influence of different factors on the aggregation effect on hemoglobin (Hb) and enzymes during the preparation of Polyhemoglobin-Superoxide dismutase-Catalase-Carbonic anhydrase (PolyHb-SOD-CAT-CA). Several factors including temperatures, pH values, Glutaraldehyde (GDA) amounts and enzymes amounts were investigated systematically to study their effects on the enzymes recoveries and polymerization rates including the Superoxide dismutase (SOD), Catalase (CAT) and Carbonic anhydrase (CA), as well as their effects on the molecular weight distribution of PolyHb-SOD-CAT-CA. Then the oxygen affinity and methemoglobin (MetHb) contents of obtained PolyHb-SOD-CAT-CA were measured to evaluate the effects of enzyme crosslinking on the properties of Polyhemoglobin (PolyHb) moieties in the molecular structure of obtained PolyHb-SOD-CAT-CA conjugate. The results showed that the enzyme recoveries and polymerization rates could be decreased with the temperatures increasing and could be generally kept stable in the physiological pH conditions, but presented only slight changes among the investigated enzyme amounts ranges. Although the GDA concentration increasing could promote the enzyme polymerization rates, the enzyme recoveries decreased in whole. The polymerization rate and molecular size of PolyHb-SOD-CAT-CA conjugate increased with the elevation of temperature and the concentration of GDA. Lastly, the P50 values, Hill coefficients, and MetHb contents of PolyHb-SOD-CAT-CA conjugate with different enzyme crosslinking degrees exhibited no obvious differences with each other. In conclusion, the polymerization reactions between enzymes and Hb molecules could be remarkably affected by temperatures, pH values, and GDA amounts, and the enzyme crosslinking presented no obvious effects on the Hb properties, especially about the oxygen affinity and oxidation degrees.

Storage Optimization of Transmission Holographic Gratings in Photohydrogels.

The development and optimization of holographic materials represent a great challenge today. These materials must be synthesized according to the characteristics that are desirable in photonic devices whose application is the object of investigation. In certain holographic sensors and biosensors, it is essential that the recording material be stable in liquid media. Furthermore, the holographic gratings stored in them must have temporal and structural stability, so that they can act as transducers of the analytical signal. Therefore, it is essential to optimize its storage in terms of the chemical composition of the material and the optical parameters of recording. This work focuses on the study of the storage optimization of unslanted transmission volume phase holograms in photohydrogels based on acrylamide and N,N'-methylenebis(acrylamide). Hydrogel matrices, also composed of acrylamide and N,N'-methylenebis(acrylamide), with different degrees of cross-linking were used and analyzed by scanning electron microscopy and UV-visible spectroscopy. The best results in terms of diffraction efficiency were reached for hydrogel matrices with an acrylamide/N,N'-methylenebis(acrylamide) molar ratio between 19.9 and 26. This relationship was also optimized in the incubator solution used to incorporate the components necessary for the formation of the holograms in the hydrogel matrices. The maximum diffraction efficiency, about 35%, was achieved when using an incubation solution with an acrylamide/N,N'-methylenebis(acrylamide) molar ratio of 4.35. The influence of the physical thickness of the hydrogel layers, the intensity, and the exposure time on the diffraction efficiency was also investigated and optimized. In addition, the behavior of the hologram was analyzed after a washing stage with PBST. A simple model that considered the effects of bending and attenuation of holographic gratings was proposed and used to obtain the optical parameters of the holograms.

Effects of thermal treatments on the fracture behaviour of a silica-filled NBR: A study on the recovery of the Mullins effect and on the stretch-induced cavity formation

This research work is focused on the study of the fracture behaviour of a silica-filled NBR. The Mullins effect and its thermally-induced recovery are initially studied performing tensile tests: comparing the material's response in uniaxial tension and pure shear deformation conditions, a lower recovery is observed in the pure shear configuration. A similar study is then performed considering the fracture behaviour of the material. Tests are performed in quasi-static loading conditions and by applying a fracture mechanics approach. The fracture toughness is evaluated as J-integral at the crack onset and at the unstable fracture initiation; further, the crack propagation is analysed and the resistance curve is obtained. The dependence of the overall fracture behaviour of the material on the applied thermal history is evaluated. Even though the crosslinking degree seems not to be affected by the thermal treatment, the fracture behaviour is modified. A correlation of these results with a change in the material's propensity to form cavities under stretching is proposed.

Production of resistant starches via citric acid modification: Effects of reaction conditions on chemical structure and final properties

Aiming to contribute to the current knowledge on the impact of reaction conditions on the chemical structure and target properties of starch citrates, in the current contribution different corn starch citrates were prepared by manipulation of reaction time, temperature and citric acid concentration. Modified starches were characterized in terms of chemical structure, morphology, crystallinity, swelling power and resistant starch content. For the first time, total substitution, crosslinking and monosubstitution degrees were quantitatively determined; and the relationship among final chemical structure, reaction conditions and target starch citrates properties was comprehensively analyzed. Products with total substitution values in the range of 0.075–0.24, crosslinking degrees in the 0.005–0.11 interval, and monosubstitution extents within the 0.05–0.12 range, were produced. By proper selection of reaction conditions products with almost 100 % of resistant starch were obtained. Results evidenced that starch citrates properties (mainly swelling power and RS content) depend on both chemical structure and the reaction conditions employed. Actually, the reaction temperature set (120 °C or 150 °C) proved to play a determinant role in the final products properties as evidenced from starch citrates with similar chemical structure and substantially different swelling and digestibility properties.

Full Face Tailored Treatments Using Hyaluronan Dermal Fillers: Biophysical Characterization for Safe and Effective Approaches

Hyaluronic acid (HA)-based dermal fillers are among the most popular non-invasive facial aesthetic treatments. To ensure an effective and safe treatment experience, knowledge of their biophysical and rheological characteristics, such as: HA concentration, molecular weight (MW), G′, and the degree of cross-linking is essential. Products with a higher MW, G′, and degree of cross-linking are more suitable for promoting volume and lift. Dermal fillers with a lower MW, G′, and degree of cross-linking can produce a soft filling effect that regulates hydration and elasticity. This review discusses how these rheological characteristics can inform treatment choice and their effects on clinical outcomes. The Aliaxin® line of HA dermal fillers, which are tailored to different clinical applications due to their rheological characteristics, highlights that extensive knowledge of the product can provide very safe and effective procedures for patients, whilst respecting their natural facial aesthetics. This review discusses studies using Aliaxin® dermal fillers for volumizing and hydrating treatments and fillers that can be used for lip augmentation. Treatment with Aliaxin® was overall very effective, with no reported adverse events. A full facial treatment using tailored dermal fillers may be a future approach to achieve an effective and safe harmonized and natural aesthetic.

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.

Recycling devulcanized EPDM to improve engineering properties of SBR rubber compounds

Ethylene propylene diene rubbers (EPDM) have gained substantial attention in automotive and industrial applications owing to their exceptional resistance against weathering and heat. Despite their advantages, the elastomeric nature of EPDM poses challenges in its recycling due to the presence of crosslinks in their chemical structure, preventing them from melting. To overcome this issue, devulcanized EPDM (EPDMd) has been developed, characterized by the effective breaking of these crosslinks. Our study focuses on common composites that include Styrene Butadiene Rubber (SBR), EPDM and silica, but with the incorporation of devulcanized EPDM (EPDMd).We have studied the mechanical, thermal, structural and dielectric properties of SBR composites containing EPDMd at variable compositions (0, 20, 40, 50, 60 phr). Employing techniques such as Thermogravimetric Analysis (TGA), Fourier Transform Infrared Spectropy (FTIR), and Scanning Electronic Microscopy (SEM), we have explored the microstructural changes driving the macroscopic effects on the measured properties.The results show that incorporating EPDMd improves the crosslinking degree and, at optimal 40 phr loading, significantly increases the mechanical properties of SBR matrix. The addition of SiO2, in general, reduce tensile strength and elongation, while increasing the Young's modulus, except for compositions around 40 phr EPDMd. The dielectric measurements are in concordance with the previous data, showing a moderation of the Maxwell–Wagner–Sillars (MWS) effect due to SiO2 in highly filled EPDMd composites at 40 phr EPDMd.

Pre-Coordination Induced Further Deamination to Create Inter-Chain Cross-Linking in Carbon Nitride for Enhanced Photocatalytic H2O2 Production.

Creating cross-linking to establish efficient inter-chain charge-transfer channels in carbon nitride represents a promising strategy for enhancing its photocatalytic capabilities. Molten salt-assisted calcining has emerged as a method for preparing cross-linked carbon nitrides. However, the precise influence of molten salts on the molecular structure of carbon nitride remains to be fully elucidated. Herein, we develop a KCl guided cross-linking reaction to preliminarily reveal the formation mechanism of cross-linking. The cross-linking reaction is initiated by the pre-coordination of amino groups with K+. Subsequent heating at high temperature converts the amino groups into chlorines. Then, dechlorination leads to the formation of cross-linking. Thus, this cross-linking reaction can be accurately described as a pre-coordination-induced, two-step deamination reaction. The pre-coordination step plays a pivotal role in the cross-linking process. Sufficient pre-coordination results in a relatively high cross-linking degree of the as-prepared CNK-2. Consequently, CNK-2 demonstrates a significantly enhanced photocatalytic H2O2 production, with a generation rate of 682 μmol L-1 h-1, about 59 times that of traditional carbon nitride.

Pore engineering of Porous Materials: Effects and Applications.

Porous materials, characterized by their controllable pore size, high specific surface area, and controlled space functionality, have become cross-scale structures with microenvironment effects and multiple functions and have gained tremendous attention in the fields of catalysis, energy storage, and biomedicine. They have evolved from initial nanopores to multiscale pore-cavity designs with yolk-shell, multishells, or asymmetric structures, such as bottle-shaped, multichambered, and branching architectures. Various synthesis strategies have been developed for the interfacial engineering of porous structures, including bottom-up approaches by using liquid-liquid or liquid-solid interfaces "templating" and top-down approaches toward chemical tailoring of polymers with different cross-linking degrees, as well as interface transformation using the Oswald ripening, Kirkendall effect, or atomic diffusion and rearrangement methods. These techniques permit the design of functional porous materials with diverse microenvironment effects, such as the pore size effect, pore enrichment effect, pore isolation and synergistic effect, and pore local field enhancement effect, for enhanced applications. In this review, we delve into the bottom-up and top-down interfacial-oriented synthesis approaches of porous structures with advanced structures and microenvironment effects. We also discuss the recent progress in the applications of these collaborative effects and structure-activity relationships in the areas of catalysis, energy storage, electrochemical conversion, and biomedicine. Finally, we outline the persisting obstacles and prospective avenues in terms of controlled synthesis and functionalization of porous engineering. The perspectives proposed in this paper may contribute to promote wider applications in various interdisciplinary fields within the confined dimensions of porous structures.

Towards high-performance polydimethylsiloxane-based materials for thermal management: A molecular dynamics study

To efficiently design high-performance polymer-based thermal interface material (TIM), it is imperative to investigate how microstructural influences thermal transport. Utilizing molecular dynamics (MD) simulations, this study examined the effects of crosslinking degree (10–40%) and alumina (Al2O3) filler doping ratios (0–23.13 wt%) on the thermomechanical behaviors of PDMS. Our findings indicated that increasing the degree of crosslinking significantly enhances thermal conductivity at lower doping rates by creating additional heat transfer channels. However, at higher doping rates, thermal conductivity improvement is mitigated due to the potential hindrance caused by fillers. Optimal thermal conductivity was observed with a 20% crosslinking degree and 14.67 wt% Al2O3 doping, achieving an 18% enhancement compared to systems without crosslinking. These results underscore the complex interplay between crosslinking and filler content in optimizing the thermal performance of PDMS-based TIMs, contributing to the advancement of materials for efficient thermal management in microelectronic devices.

Influence of Epoxy Resin Interlayer Interfaces on Electrical Tree Growth and Breakdown Characteristics.

The solid-solid insulation interface structure is a typical interface in extra-high-voltage power equipment, in which the multilayer epoxy resin material is a key component in the insulation structure of the power equipment, and the study of its interface characteristics is the most important. In this paper, epoxy-epoxy cross-linking interface specimens were prepared through experiments, and the degree of cross-linking between the interfaces was analyzed by changing the ratio of the curing agent and adding hydroxyl-terminated liquid nitrile rubber (HTBN) particles; it can be concluded that there exists a weak cross-linking reaction between the interfaces. The electrical tree measurement and alternating current (AC) breakdown test platform were set up, and three different cases of no interface, the electric field direction parallel to the interface, and the electric field direction perpendicular to the interface were tested, through which it was concluded that the existence of the interface inhibited the development of the electrical tree. For the three different cases of AC breakdown tested, it was concluded that the presence of an interface enhances the AC breakdown strength when the electric field direction is parallel to the interface and decreases the AC breakdown strength when the electric field direction is perpendicular to the interface through the interface, affecting the charge transport.

Lightweight, compressible, elastic resorcinol-formaldehyde aerogels with cobalt-ligand-enhanced cross-linked skeletons

Resorcinol-formaldehyde (RF) aerogel materials exhibit remarkable properties such as low density, ablation resistance (high residual carbon rate), easily regulated pore structure and low thermal conductivity, making them promising for applications in adsorption, medicine and aerospace, among others. However, since their inception, RF aerogels have suffered from disadvantages such as brittleness and long preparation cycles, which have severely limited their widespread use. In order to improve the mechanical properties of RF aerogels, this paper presents a new synthetic route for obtaining strong elastic properties without introducing additional fiber reinforcement. Here, a lightweight, compressible, elastic resorcinol-formaldehyde aerogel with cobalt-ligand-enhanced cross-linked skeletons was prepared by sol-gel and freeze-drying methods using an alkali metal salt (cobalt (II) acetate) as a cross-linking agent and sodium acetate as a catalyst. The coordination of metal ions (Co2+) with resorcinol resulted in the formation of a structure analogous to a metal-phenolic network (MPN), which altered the crosslinking mode and degree of crosslinking of the RF aerogel. This process led to the thickening of the skeletal structure of the sample. Concurrently, a multilayered pore structure was generated within the interior under the appropriate pH conditions, which contributed to the strengthening of the skeleton of the samples and a reduction in thermal conductivity. The obtained RF-Co aerogel can withstand 68.6 % compression change without fracture and shows good elastic deformation at 35 % compression rate, while the aerogel exhibits low thermal conductivity (0.039 W (m K)−1) and low density (0.09 g cm−3).

Impact of Crosslinking Degree on Chitosan and Oxidized Guar Gum‐Based Injectable Hydrogels for Biomedical Applications

Impact of Crosslinking Degree on Chitosan and Oxidized Guar Gum‐Based Injectable Hydrogels for Biomedical Applications

Polymer-Gel-Derived PbS/C Composite Nanosheets and Their Photoelectronic Response Properties Studies in the NIR

Non-conjugated polymer-derived functional nanocomposites are one of the important ways to develop multifunctional hybrids. By increasing the degree of crosslinking, their photophysical properties can be improved. PbS is a class of narrow bandgap infrared active materials. To avoid aggregation and passivation of the surface defects of PbS nanomaterials, a large number of organic and inorganic ligands are usually used. In this study, PbS/C composite nanosheets were synthesized with Pb2+ ion-crosslinked sodium alginate gel by one-pot carbonization. The resulting nanosheets were coated on untreated A4 printing paper, and the electrodes were the graphite electrodes with 5B pencil drawings. The photocurrent signals of the products were measured using typical 650, 808, 980, and 1064 nm light sources. The results showed that the photocurrent switching signals were effectively extracted in the visible and near-infrared regions, which was attributed to the mutual passivation of defects during the in situ preparation of PbS and carbon nanomaterials. At the same time, the resulting nanocomposite exhibited electrical switching responses to the applied strain to a certain extent. The photophysical and defect passivation mechanisms were discussed based on the aggregation state of the carbon hybrid and the interfacial electron interaction. This material would have potential applications in broadband flexible photodetectors, tentacle sensors, or light harvesting interdisciplinary areas. This study provided a facile approach to prepare a low-cost hybrid with external stimulus response and multifunctionality. These results show that the interfacial charge transfer is the direct experimental evidence of interfacial interaction, and the regulation of interfacial interaction can improve the physical and chemical properties of nanocomposites, which can meet the interdisciplinary application. The interdisciplinary and application of more non-conjugated polymer systems in some frontier areas will be expanded upon.

Quantitative characterization of the crosslinking degree of hydroxypropyl guar gum fracturing fluid by low-field NMR

As a widely used water-based fracturing fluid, the performance of hydroxypropyl guar gum fracturing fluid is closely related to the degree of crosslinking, the quantitative characterization of which can reveal a detailed crosslinking mechanism and guide the preparation of fracturing fluid gels with an excellent performance. However, the commonly used high-temperature rheology method for evaluating the performance of fracturing fluids only qualitatively reflects the degree of crosslinking. In this study, low-field nuclear magnetic resonance (LF-NMR) was used to characterize the degree of crosslinking in guar gum fracturing fluid gels. The spin-spin relaxation time of the H proton in guar gum was molecularly analyzed using LF-NMR. The viscoelastic properties met the requirements when the crosslinking degree of the gel was 88–94 %. The transformation of the linear structure into a membrane structure during the crosslinking process of the guar gum fracturing fluid was confirmed by freeze-drying and scanning electron microscopy (SEM) from a microscopic perspective. The changing trend of the microstructure and viscoelastic properties of the fracturing fluid gel under different crosslinker dosages was consistent with changes in the degree of crosslinking. The LF-NMR test process is non-destructive to the gel structure, and the test results demonstrate good accuracy and repeatability.