Glycidyl Methacrylate Research Articles

Construction of Zwitterionic Coatings with Lubricating and Anti-Adhesive Properties for Invisible Aligner Applications.

Invisible aligners have been widely used in orthodontic treatment but still present issues with plaque formation and oral mucosa abrasion, which can lead to complicated oral diseases. To address these issues, hydrophilic poly(sulfobetaine methacrylate) (polySBMA) coatings with lubricating, antifouling, and anti-adhesive properties have been developed on the aligner materials (i.e., polyethylene terephthalate glycol, PETG) via a simple and feasible glycidyl methacrylate (GMA)-assisted coating strategy. Poly(GMA-co-SBMA) was grafted onto the aminated PETG surface via the ring-opening reaction of GMA (i.e., "grafting to" approach to obtain G-co-S coating), or a polySBMA layer was formed on the GMA-grafted PETG surface via free radical polymerization (i.e., "grafting from" approach to obtain G-g-S coating). The G-co-S and G-g-S coatings significantly reduced the friction coefficient of PETG surface. Protein adsorption, bacterial adhesion, and biofilm formation on the G-co-S- and G-g-S-coated surfaces were significantly inhibited. The performance of the coatings remained stable after storage in air or artificial saliva for 2 weeks. Both coatings demonstrated good biocompatibility in vitro and did not cause irritation to the oral mucosa of rats in vivo over 2 weeks. This study proposed a promising strategy for the development of invisible aligners with improved performance, which is beneficial for oral health treatment. This article is protected by copyright. All rights reserved.

Enhancing the Delamination Efficiency of Polyimide-Copper Bilayers with UV/Heat-Activated Foamable Adhesive: Insights and Applications.

This study explores the adhesive properties of copolymers comprising glycidyl methacrylate (GMA) and 3-(trimethoxysilyl)propyl methacrylate (MPTMS), focusing on their suitability for adhesive applications. Peel resistance measurements revealed a substantial impact of the GMA/MPTMS ratio on adhesion capabilities, identifying an optimal ratio of 30/70 for copolymerization with tert-butyl acrylate (tBA) to improve foaming performance. tBA, a foaming monomer activated by a photoacid generator and heat, enhances the copolymerized adhesive's adhesion strength and foamability for postuse delamination. Chemical structure analysis through Nuclear magnetic resonance (NMR) and Fourier-transform infrared spectroscopy (FTIR) confirmed successful polymerization, while rheological properties indicated decreased complex viscosity and adhesive strength with an increasing tBA content. The deprotection of the t-butyl group facilitated foam formation, supported by morphology analysis. These findings provide insights into foamable adhesive development with potential applications in delamination processes and implications for further exploration in polymer adhesion.

Surface thermal-curing phosphorus-containing coated rigid polyurethane foam with highly-efficient flame retardancy and reinforced mechanical property

A phosphorous-containing HEMAP–co–GMA (HPG) prepolymer was successfully prepared by the ring-opening reaction of glycidyl methacrylate (GMA) and 2–hydroxyethyl methacrylate phosphate (HEMAP) as monomers, and flame retardant HEMAP–GMA copolymer (HPG) coating on the surface of rigid polyurethane foam (RPUF) was further fabricated by free-radical thermal-curing. The HPG coating endowed RPUF excellent flame retardancy and fire hazardous safety. The HPG coated on RPUF (HPG/RPUF) reached UL94 V–0 rating, and the limited oxygen index value of the HPG-2/RPUF improved from 19.0 % of RPUF to 27.8 %. The cone calorimetric test results showed that the total heat release and mean peak heat release rate values of the HPG-2/RPUF reduced by 79.6 % and 54.6 % compared to those of RPUF, respectively. The flame–retardant mechanism of HPG/RPUG was speculated the synergistic flame retardant effect between the barrier of the dense char layer and the inhibition of phosphorus–containing free–radicals. The three–dimensional crosslinked HPG coating not only provided HPG/RPUF excellent water resistance, but also enhanced compressive properties and heat–insulation. The highly efficient flame–retardant HPG coating has great potential in fire protection of the heat insulation foams.

PTFE-g-GMA graft copolymer synthesis promoted by oxidative gamma-rays method and characterization

The functionalization of polymeric matrices through graft polymerization offers various advantages by providing new properties, allowing for additional chemical reactions that the matrix alone could not undergo or that would require drastic chemical conditions to occur. In this work, epoxy groups were incorporated through a graft polymer of poly(glycidyl methacrylate), using a prefunctionalization with peroxide groups in the polytetrafluoroethylene matrix through gamma radiation. These peroxide groups were subsequently used as radical chemical initiators in the graft polymerization reaction of glycidyl methacrylate. The graft polymerization reaction was studied based on the absorbed dose, monomer concentration, reaction time, and temperature.Graphical abstract

Towards the preparation of sustainable superplasticizers for geopolymeric pastes via radiation-induced grafting of sulfonic group-bearing monomers onto corn starch

To address escalating environmental and sustainability concerns of petroleum-based superplasticizers (SPs), this work aims to develop sustainable and eco-friendly starch-based SPs using gamma radiation for maintaining the desired workability of geopolymeric pastes. Specifically, two green SPs were prepared from starch via radiation-induced grafting of two sulfonic group-bearing monomers, namely 2-acrylamido-2-methylpropane sulfonic acid (AMPS) and 4-styrene sulfonic acid sodium salt (Na4SS). The grafting reaction was improved by initial modification of starch with glycidyl methacrylate to insert vinyl groups into the starch backbone. The modified starch samples were characterized by a variety of analytical techniques such as FTIR, 1H NMR, EDX, SLS, and viscometry. The prepared SPs exhibited high stability in aqueous 5 % NaOH. The effect of the prepared SPs on the fresh properties of GGBFS/MK geopolymer was studied using the mini slump test, zeta potential, adsorption capacity, and setting time. They significantly improved the paste flowability and dispersion compared to the control. Notably, the aromatic Na4SS-grafted starch displayed a comparable enhancement to the commercial PNS, while outperforming the aliphatic AMPS-grafted sample. This emphasizes the potential of these green SPs to address the challenges posed by the petroleum-based SPs and maximize the benefit of using starch as a green renewable resource.

Synthesis and study of free radical graft polymerization of glycidyl methacrylate on gamma-irradiated graphene oxide

This study reports on the synthesis of a novel poly (glycidyl methacrylate) (PGMA) grafted graphene oxide (GO) by using a free radical-induced emulsion graft polymerization method. PGMA was grafted onto a gamma irradiated and vinyl functionalized GO substrate, and the parameters of graft polymerization (i.e., the concentration of monomer, initiator, and surfactant) were optimized to achieve the maximum grafting percentage. Remarkably, a PGMA grafting percentage of up to 2626 % was obtained under the optimal reaction conditions. The developed materials were characterized by different characterization techniques including Fourier-transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) analysis, thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The presence of characteristic peaks of PGMA in FTIR spectra and changes in morphology of GO sheets after the grafting process confirmed the successful PGMA grafting onto GO. The thermal stability of the grafted samples was also significantly enhanced and increased with an increase in grafting percentage. This work discloses the tailoring of the properties of nanohybrid material obtained by free radical-induced emulsion graft polymerization. The prepared PGMA grafted GO nanohybrids can be further modified to develop adsorbents for metal uptake.

β-Lactoglobulin-based aerogels: Facile preparation and sustainable removal of organic contaminants from water

Economically and efficiently removing organic pollutants from water is still a challenge in wastewater treatment. Utilizing environmentally friendly and readily available protein-based natural polymers to develop aerogels with effective removal performance and sustainable regeneration capability is a promising strategy for adsorbent design. Here, a robust and cost-effective method using inexpensive β-lactoglobulin (BLG) as raw material was proposed to fabricate BLG-based aerogels. Firstly, photocurable BLG-based polymers were synthesized by grafting glycidyl methacrylate. Then, a cross-linking reaction, including photo-crosslinking and salting-out treatment, was applied to prepared BLG-based hydrogels. Finally, the BLG-based aerogels with high porosity and ultralight weight were obtained after freeze-drying. The outcomes revealed that the biocompatible BLG-based aerogels exhibited effective removal performance for a variety of organic pollutants under perfectly quiescent conditions, and could be regenerated and reused many times via a simple and rapid process of acid washing and centrifugation. Overall, this work not only demonstrates that BLG-based aerogels are promising adsorbents for water purification but also provides a potential way for the sustainable utilization of BLG.

Development of functionalized poly(lactide) films with chitosan via SI-SARA ATRP as scaffolds for neuronal cell growth

Polylactic acid (PLA), a polymer derived from renewable resources, is gaining increasing attention in the development of biomedical devices due to its cost-effectiveness, low immunogenicity, and biodegradability. However, its inherent hydrophobicity remains a problem, leading to poor cell adhesion features. On this basis, the aim of this work was to develop a method for functionalizing the surface of PLA films with a biopolymer, chitosan (CH), which was proved to be a material with intrinsic cell adhesive properties, but whose mechanical properties are insufficient to be used alone. The combination of the two polymers, PLA as a bulk scaffold and CH as a coating, could be a promising combination to develop a scaffold for cell growth. The modification of PLA films involved several steps: aminolysis followed by bromination to graft amino and then bromide groups, poly(glycidyl methacrylate) (PGMA) grafting by surface-initiated supplemental activator and reducing agent atom transfer radical polymerization (SI-SARA ATRP) and finally the CH grafting. To prove the effective adhesive properties, conjugated and non-conjugated films were tested in vitro as substrates for neuronal cell growth using differentiated neurons from human induced pluripotent stem cells. The results demonstrated enhanced cell growth in the presence of CH.

Impact of a Lightly Branched Star Polyelectrolyte Architecture on Polyelectrolyte Complexes.

The effect of charge density in blocky and statistical linear polyelectrolytes on polyelectrolyte complex (PEC) properties has been studied with the finding that increased charge density in a polyelectrolyte tends to increase the salt resistance and modulus of a PEC across various polyelectrolyte pairs. Here, we demonstrate the ability to orthogonally alter PEC salt resistance while maintaining rheological properties and internal structure by going from linear to lightly branched architectures with similar total degrees of polymerization. Using a model system built around glycidyl methacrylate (GMA) and thiol-epoxy "click" functionalization, we create a library of homologous linear, 4-armed, 6-armed, and 8-armed star polyelectrolytes. The PECs formed from these model polyelectrolyte pairs are then characterized via optical microscopy, rheology, and small-angle X-ray scattering to evaluate their salt resistance, mechanical properties, and internal structure. We argue that our results are due to the difference between linear charge density or charge per unit length along backbone segments for each polyelectrolyte and spatial charge density, the number of charges per unit volume of the polyelectrolyte prior to complexation. Our findings suggest that linear charge density is the dominant factor in determining intermolecular interactions of the complex, leading to identical rheological and structural behavior, whereas the spatial charge density primarily influences the stability of the complexes. These distinct mechanisms for altering various sought-after PEC properties offer greater potential applications in precision design of polyelectrolyte complex materials.

Прививочная полимеризация акриловых мономеров на полиэтиленовую поверхность (обзор)

A search and review of English-language scientific literature about the graft copolymerization of acrylic monomers onto a solid-phase polymeric surface has been carried out. Grafting onto plates and films of high- and low-density polyethylene is considered. The monomers used were acrylic and methacrylic acids, glycidyl acrylate and glycidyl methacrylate, etc., and the main method was UV photopolymerization with an initiator – benzophenone, etc. Problems of graft polymerization in terms of surface modification of polymeric materials are touched upon, and possible areas of their application are outlined.

Controlled Amphiphilicity and Thermo-Responsiveness of Functional Copolymers Based on Oligo(Ethylene Glycol) Methyl Ether Methacrylates.

In this work, comb homopolymers as well as comb-type copolymers of thermo-responsive oligo(ethylene glycol methyl ether methacrylate)s, OEGMAs, with various chain lengths (DEGMA, PEGMA500, and PEGMA950 containing 2, 9, or 19 repeating ethylene glycol units, respectively) were synthesized through free radical (co)polymerization. For the copolymers, either the functional hydrophobic glycidyl methacrylate (GMA) or the inert hydrophilic N,N-dimethylacrylamide (DMAM) were selected as comonomers. The self-assembly and thermo-responsive behavior of the products was investigated through Nile Red fluorescence probing, turbidimetry, and dynamic light scattering (DLS). Interestingly, it was found that all OEGMA-based homopolymers exhibit a tendency to self-organize in aqueous media, in addition to thermo-responsiveness. The critical aggregation concentration (CAC) increases with the number of repeating ethylene oxide units in the OEGMA macromonomers (CAC was found to be 0.003, 0.01, and 0.03% w/v for the homopolymers PDEGMA, PPEGMA500, and PPEGMA950, respectively). Moreover, the CAC of the copolymers in aqueous media is highly affected by the incorporation of hydrophobic GMA or hydrophilic DMAM units, leading to lower or higher values, respectively. Thus, the CAC decreases down to 0.003% w/v for the GMA-richest copolymer of PEGMA950, whereas CAC increases up to 0.01% w/v for the DMAM-richest copolymer of DEGMA. Turbidimetry and DLS studies proved that the thermo-sensitivity of the polymers is governed by several parameters such as the number of repeating ethylene glycol groups in the side chains of the OEGMAs, the molar percentage of the hydrophobic or hydrophilic comonomers, along with the addition of salts in the aqueous polymer solutions. Thus, the cloud point of the homopolymer PDEGMA was found at 23 °C and it increases to 33.5 °C for the DMAM-richest copolymer of DEGMA. Lastly, the formation of a hydrogel upon heating aqueous mixtures of the GMA-comprising copolymers with silica nanoparticles overnight is strong evidence of the functional character of these polymers.

Preparation and Performance Study of Boron Adsorbent from Plasma-Grafted Polypropylene Melt-Blown Fibers.

In this study, the plasma graft polymerization technique was used to graft glycidyl methacrylate (GMA) onto polypropylene (PP) melt-blown fibers, which were subsequently aminated with N-methyl-D-glucamine (NMDG) by a ring-opening reaction, resulting in the formation of a boron adsorbent denoted as PP-g-GMA-NMDG. The optimal conditions for GMA concentration, grafting time, grafting temperature, and the quantity of NMDG were determined using both single factor testing and orthogonal testing. These experiments determined the optimal process conditions to achieve a high boron adsorption capacity of PP-g-GMA-NMDG. Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersion spectrum analysis (EDS), and water contact angle measurements were performed to characterize the prepared adsorbent. Boron adsorption experiments were carried out to investigate the effects of pH, time, temperature, and boron concentration on the boron adsorption capacity of PP-g-GMA-NMDG. The adsorption isotherms and kinetics of PP-g-GMA-NMDG for boron were also studied. The results demonstrated that the adsorption process followed a pseudo-second-order kinetic model and a Langmuir isothermal model. At a pH of 6, the maximum saturation adsorption capacity of PP-g-GMA-NMDG for boron was 18.03 ± 1 mg/g. In addition, PP-g-GMA-NMDG also showed excellent selectivity for the adsorption of boron in the presence of other cations, such as Na+, Mg2+, and Ca2+, PP-g-GMA-NMDG, and exhibited excellent selectivity towards boron adsorption. These results indicated that the technique of preparing PP-g-GMA-NMDG is both viable and environmentally benign. The PP-g-GMA-NMDG that was made has better qualities than other similar adsorbents. It has a high adsorption capacity, great selectivity, reliable repeatability, and easy recovery. These advantages indicated that the adsorbents have significant potential for widespread application in the separation of boron in water.

Modified Bitumen Materials from Kazakhstani Oilfield

The oil bitumen BND 90/130, produced at the “LLP SP Caspi Bitum” with the modifier, which consists of copolymer of ethylene with butyl acrylate and glycidyl methacrylate taken in an amount of 0.5–1.6 wt%, and the tire reclaim (4–20 wt%), which is the destructate of mesh elastomers of different chemical nature, was modified; possibility of using the developed bitumen-elastomer binders in road asphalt concrete was justified. Modification of bitumen with a copolymer of ethylene with butyl acrylate and glycidyl methacrylate leads to an improvement in the properties of road bitumen: the softening point, hardness, deformability at low temperatures, elasticity, and adhesion to metal and mineral filler increase. It was shown that ethylene with butyl acrylate and glycidyl methacrylate chemically interacts with the functional groups of bitumen asphaltenes through the epoxy group of glycidyl methacrylate. Analysis of the spectra and group composition indicates an increased content of high molecular weight asphaltenes in the modified bitumen with a slight increase in structuring resins. It has been established that bitumen modified with rubber crumbs of 0.6–1.0 mm in size has high elasticity. The most effective composition of a bitumen-regenerated composite material based on tire reclaim has been determined. In terms of the totality of physicochemical and operational characteristics and comparative cost, the most acceptable is the bitumen-regenerated composition (with a regenerate content of 20%) and is superior in the complex of properties to bitumen modified with an optimal content of ethylene with butyl acrylate and glycidyl methacrylate (1.6%). The technology for modifying bitumen with tire reclaim is less time-consuming, more economically profitable, and environmentally effective, since it utilizes large-tonnage waste of worn-out tires. The resulting bitumen-polymer compositions have a high positive set of properties: softening point, hardness, elasticity, frost resistance, and low-temperature characteristics.

Improvement in non‐linear electrical conductivity of silicone rubber by incorporating zinc oxide fillers and grafting small polar molecules

AbstractSilicone rubber (SiR) is commonly used in reinforced insulation parts for high‐voltage direct current (HVDC) cable accessories due to its excellent insulation, elasticity, and high‐temperature resistance. HVDC cable accessories always suffer from the local electric field concentration due to the electrical conductivity mismatch between reinforced insulation and main insulation, which can ultimately lead to electric breakdown. The non‐linear conductive composites based on SiR have the ability to adaptively adjust the distribution of the electric field in cable accessories. This is expected to solve the problem of localised electric field concentration. The zinc oxide (ZnO) and glycidyl methacrylate (GMA) are used as fillers and grafted modifier respectively to improve the non‐linear electrical conductivity of ZnO/SiR‐GMA composites. The results indicate that grafting GMA can increase electrical conductivity of SiR, while doping ZnO filler enables SiR to have non‐linear conductivity characteristics. The combination of doping and grafting modification of the composites achieves excellent non‐linear conductive properties at lower ZnO filler content. Additionally, the mechanical properties of the modified composites are enhanced. The simulation results indicate that ZnO/SiR‐GMA is the most effective material for homogenising the electric field when used as reinforced insulation for cable intermediate joints.

Polymeric monolithic columns based on natural wood for rapid purification of targeted protein

With multiscale hierarchical structure, wood is suitable for a range of high-value applications, especially as a chromatographic matrix. Here, we have aimed to provide a weak anion-exchange polymeric monolithic column based on natural wood with high permeability and stability for effectively separating the targeted protein. The wood-polymeric monolithic column was synthesized by in situ polymerization of glycidyl methacrylate and ethylene glycol dimethacrylate in wood, and coupled with diethylaminoethyl hydrochloride. The wood-polymeric monolithic column can be integrated with fast-protein liquid chromatography for large-scale protein purification. According to the results, the wood-polymeric monolithic column showed high hydrophilicity, permeability and stability. Separation experiments verified that the wood-polymeric monolithic column could purify the targeted protein (spike protein of SARS-COV-2 and ovalbumin) from the mixed proteins by ion exchange, and the static adsorption capacity was 33.04 mg mL−1 and the dynamic adsorption capacity was 24.51 mg mL−1. In addition, the wood-polymerized monolithic column had good stability, and a negligible decrease in the dynamic adsorption capacity after 20 cycles. This wood-polymerized monolithic column can provide a novel, efficient, and green matrix for monolithic chromatographic columns.

Achieving Enhanced Dielectric and Energy Storage Performance in Poly(vinyl chloride-glycidyl methacrylate) through Tuning Interchain Interactions.

Glassy polymer dielectrics exhibit significant advantages in energy storage density and discharge efficiency; however, their potential application in thin-film capacitors is limited by the complexity of the production process, rising costs, and processing challenges arising from the brittleness of the material. In this study, a small amount of the polar monomer glycidyl methacrylate (GMA) was copolymerized with vinyl chloride (VC) using a highly integrated and precisely controlled process. This effectively facilitated the bulk synthesis of P(VC-GMA) copolymers, aimed at enhancing the dielectric properties and energy storage capabilities of the copolymer. Moreover, the incorporation of GMA into PVC induces significant alterations in the structural sequence of the copolymer, resulting in an enhancement of interchain interactions that ultimately contribute to an increase in the modulus and improved breakdown strength. With a GMA content of 2.4 mol %, P(VC-GMA) exhibits a significant enhancement in discharge energy density, surpassing that of a pure PVC copolymer, while maintaining high discharge efficiency and stability. The finding of this study paves the way for future advancements in high-energy-storage polymer dielectrics, thereby expanding the scope of advanced dielectric materials.

Porous Morphology of High Grafting Density Mixed Polyelectrolyte Brushes Grown from a Y-Inimer Coating.

Mixed A/B polyelectrolyte (PE) brushes of opposite charges are grown from a Y-shaped initiator-bearing coating to facilitate intimate mixing of the A and B polyelectrolytes in a 1:1 grafting ratio. The design of the Y-shaped inimer includes both ATRP and NMP initiators attached to a common Y-junction. A copolymer of a Y-shaped inimer with glycidyl methacrylate is cross-linked to the substrate resulting in a stable ultrathin coating decorated with Y-shaped initiators. Weak PE A/B mixed brushes based on poly(methacrylic acid)/poly(2-vinylpyridine) (PMAA/P2VP) with a high grafting density of ∼1 chain/nm2 are grown by surface-initiated ATRP and NMP, respectively. Detailed morphological characterization of the PMAA/P2VP brushes in response to pH changes reveals a nanoporous morphology under conditions that maximize complex coacervate formation between oppositely charged brushes. The charge ratio between the A and B brushes is varied via the composition of the brushes to further study the morphology evolution. The effect of intimate contact between the A and B brushes on the morphology is probed by comparing with a mixed A/B PE system with random fluctuations in grafting composition. A quantitative and qualitative study of the pore evolution with pH as well as charge composition is presented using a combination of atomic force microscopy, water contact angle measurement, and image analysis using Gwyddion software. These studies demonstrate that the porous morphology is enhanced and most uniform when the brushes are grown from the Y-inimer, indicating that a 1:1 grafting ratio and intimate contact between A and B brushes are essential.

Harnessing leather waste in polymer matrix for sustainable smart shape‐stable phase change materials

AbstractThe utilization of leather waste (LW) in a polyurethane (PU) matrix makes a smart and novel shape stable phase change material (SSPCM). This is essential for sustainability as it reduces landfill waste after use. The PU is synthesized in bulk with a 90% yield, using biodegradable polycaprolactone diol and bio‐based polyol (castor oil), along with tolylene‐2,4‐diisocyanate. PL and PLG composites are prepared by blending of constituent components PU (P), LW (L), and poly(glycidyl methacrylate) (PGMA, G), as specified by their code names. Role of LW (hydrogen bonding and chemical crosslinking) and morphology are elucidated by FTIR and SEM, respectively. Self‐healing time (2 h), shape fixity ratios (Rf) (PL: 60–80% and PLG: 60–70%) and shape recovery ratios (Rr) (100% for both) are determined at 60°C. PLG displays faster shape recovery in water (<30 s) compared to air (>300 s). Shape stability and thermal properties of the SSPCM are examined using the temperature responsive leakage study, TGA, and DSC. This research introduces a new approach for using leather waste (LW) in SSPCM, with self‐healing and 100% Rr. This material may find application where SSPCM with high durability and flexibility is essential such as textile and footwear materials.

Preparation and Adsorption Performance of Boron Adsorbents Derived from Modified Waste Feathers.

This research focuses on modifying discarded feathers by grafting glycidyl methacrylate (GMA) onto their surface through thiolation, followed by an epoxy ring-opening reaction with N-methyl-D-glucamine (NMDG) to synthesize feather-based boron adsorbents. Optimization of the adsorbent preparation conditions was achieved through single-factor experiments, varying temperature, time, GMA concentration, and initiator dosage. The synthesized adsorbent (F-g-GMA-NMDG) underwent characterization using Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The adsorption behavior of the adsorbent was studied, and its boron adsorption capacity at different temperatures was determined through static adsorption kinetic curves. Analysis of adsorption isotherms, kinetics, and thermodynamics was conducted. Results indicate that the boron adsorption process by F-g-GMA-NMDG follows a pseudo-second-order model. The adsorption process is endothermic, with higher temperatures promoting adsorption efficiency. Gibbs free energy (ΔG) confirms the spontaneity of the adsorption process. Enhanced adsorption efficacy was observed under neutral and acidic pH conditions. After four cycles, the adsorbent maintained its adsorption efficiency, demonstrating its stability and potential for reuse. This study provides novel insights into both the treatment of discarded feathers and the development of boron adsorbents.

An in situ strategy to produce high-performance composite thermal adhesives with excellent bonding, thermal transfer and adjustable electrical performance based on a designer hyperbranched epoxy copolymer

Thermally conductive adhesives (TCAs) have attracted considerable attentions in recent years as they can simultaneously promote interfacial bonding and thermal transfer. So far, a lot of strategies have been explored for producing them. Among them, modifying adhesive resins with thermally conductive nanofillers is one of the most frequently reported methodologies, which often involves complicated process and tedious procedures. We herein report a facile strategy for producing TCAs via an in situ process with the assistance of a designer hyperbranched epoxy copolymer, HBPE@PGMA. This copolymer consists of a hyperbranched polyethylene (HBPE) core and multiple poly (glycidyl methacrylate) (PGMA) side chains, which can be synthesized under mild conditions by a two-step polymerization process. As a stabilizer, this copolymer is found to effectively promote the exfoliation of hexagonal boron nitride (h-BN), natural graphite or multi-walled carbon nanotubes (MWCNTs) in chloroform under sonication, rendering boron nitride nanosheets (BNNS), graphene and individually dispersed MWCNT, respectively. Meanwhile, some of the copolymer can be irreversibly adsorbed on the resultant nanofiller surface based on the noncovalent CH-π interactions. This makes them well dispersible in chloroform and allows us to obtain high-performance TCAs from their dispersions via in situ process directly using the copolymer as matrix. The resultant TCAs simultaneously exhibit excellent interfacial bonding, thermal transfer and adjustable electrical performance. This strategy paves a way for producing high-performance TCAs through in situ process with relatively simple process.