Polyacrylate Research Articles

Strong and Thermo-Switchable Gel Adhesion Based on UCST-Type Phase Transition in Deep Eutectic Solvent.

It remains a great challenge to achieve strong and reversible hydrogel adhesion. Hydrogel adhesives also suffer from poor environmental stability due to dehydration. To overcome these problems, here reversible adhesive gels are designed using a new switching mechanism and new solvent. For the first time, the study observes UCST (upper critical solution temperature)-type thermosensitive behaviors of poly(benzyl acrylate) (PBnA) polymer and gel in menthol:thymol deep eutectic solvents (DESs). The temperature-induced phase transition allows adjusting cohesive force, and hence adhesion strength of PBnA gels by temperature. To further improve the mechanical and adhesion properties, a peptide crosslinker is used to allow energy dissipation when deforming. The resulting eutectogel exhibits thermal reversible adhesion with a high switching ratio of 14.0. The adhesion strength at attachment state reaches 0.627MPa, which is much higher than most reversible adhesive hydrogels reported before. The low vapor pressure of DES endows the gel excellent environmental stability. More importantly, the gel can be repeatedly switched between attachment and detachment states. The strong and reversible gel adhesive is successfully used to design soft gripper for the transport of heavy cargos and climbing robot capable of moving on vertical and inverted surface in a manner similar to gecko.

Low-temperature curable permalloy-based soft magnetic composites for megahertz applications

This paper proposed low-temperature curable soft magnetic composites (SMCs) cores that consisted of permalloy powders and acrylic polymer (Trimethylpropane triacrylate, or TMPTA) for high-frequency applications. The effect of TMPTA content, compaction pressure and curing temperature on the magnetic properties of synthesized cores were investigated. The coated TMPTA insulating layer can effectively increase the electrical resistivity of the core and thereby improve the frequency characteristics. The magnetic performance of cores depends on the distribution and actual content of the TMPTA after pressing although the polymer content in the mixture is increased from 2 wt% to 6 wt%. As the compaction pressure increases from 100 MPa to 400 MPa, the relative permeability of the core increases but its imaginary part of the permeability has almost no change until 10 MHz. The increased curing temperature can increase the initial permeability of the cores but deteriorates the frequency stability and greatly increase the imaginary part of the permeability. It was noted that the core with 5 % TMPTA content, compacted at 400 MPa and cured at 200 °C has the best frequency stability, the lowest imaginary part of the permeability and acceptable real permeability over 30. It is beneficial for high frequency operation of power electronics.

A Lung-Expressing mRNA Delivery Platform with Tunable Activity in Hypoxic Environments.

Messenger RNA (mRNA) delivery platforms often facilitate protein expression in the liver following intravenous injection and have been optimized for use in normally oxygenated cells (21% O2 atmosphere). However, there is a growing need for mRNA therapy in diseases affecting non-liver organs, such as the lungs. Additionally, many diseases are characterized by hypoxia (<21% O2 atmosphere), a state of abnormally low oxygenation in cells and tissues that can reduce the efficacy of mRNA therapies by upwards of 80%. Here, we report a Tunable Lung-Expressing Nanoparticle Platform (TULEP) for mRNA delivery, whose properties can be readily tuned for optimal expression in hypoxic environments. Briefly, our study begins with the synthesis and characterization of a novel amino acrylate polymer that can be effectively complexed with mRNA payloads into TULEPs. We study the efficacy and mechanism of mRNA delivery using TULEP, including analysis of the cellular association, endocytosis mechanisms, endosomal escape, and protein expression in a lung cell line. We then evaluate TULEP under hypoxic conditions and address hypoxia-related deficits in efficacy by making our system tunable with adenosine triphosphate (ATP). Finally, we conclude our study with an in vivo analysis of mRNA expression, biodistribution, and tolerability of the TULEP platform in mice. In presenting these data, we hope that our work highlights the utility of TULEPs for tunable and effective mRNA delivery while more broadly highlighting the utility of considering oxygen levels when developing mRNA delivery platforms.

Radiation-Induced Synthesis and Superparamagnetic Properties of Ferrite Fe3O4 Nanoparticles.

Ultra-small magnetic Fe3O4 nanoparticles are successfully synthesized in basic solutions by using the radiolytic method of the partial reduction in FeIII in the presence of poly-acrylate (PA), or by using the coprecipitation method of FeIII and FeII salts in the presence of PA. The optical, structural, and magnetic properties of the nanoparticles were examined using UV-Vis absorption spectroscopy, high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and SQUID magnetization measurements. The HRTEM and XRD analysis confirmed the formation of ultra-small magnetite nanoparticles in a spinel structure, with a smaller size for radiation-induced particles coated by PA (5.2 nm) than for coprecipitated PA-coated nanoparticles (11 nm). From magnetization measurements, it is shown that the nanoparticles are superparamagnetic at room temperature. The magnetization saturation value Ms = 50.1 A m2 kg-1 of radiation-induced nanoparticles at 60 kGy is higher than Ms = 18.2 A m2 kg-1 for coprecipitated nanoparticles. Both values are compared with nanoparticles coated with other stabilizers in the literature.

Highly flexible liquid metal/photocurable polymer electrodes via direct laser patterning

A highly flexible electrode was fabricated using eutectic gallium-indium (eGaIn) liquid metal combined with an ultraviolet (UV)-curable polyurethane acrylate (PUA) polymer. The eGaIn liquid metal electrodes prepared by a negative-type direct patterning technique using a UV pulse laser can eliminate the need for complex photolithography masks. The optimal UV pulsed laser peak fluence was ∼1.43 J/cm2 to pattern and sinter the eGaIn/PUA composite electrode simultaneously. The laser-patterned eGaIn/PUA composite electrode under the optimal laser condition exhibited a remarkable electrical conductivity of 6.33 × 105 S/m with a patterning resolution of ∼40 μm. Moreover, the resistance of the electrode only deteriorated by 0.95% after 50,000 cycles of severe cyclic folding at a peak strain of 2.5% with a bending radius of 1 mm, demonstrating its exceptional flexibility and durability. These easily patterned eGaIn flexible electrodes via direct laser patterning techniques hold great promise for applications in wearable and flexible electronic devices that require extreme flexibility.

Engineering Water‐Stiffening Polymers via PEG‐Sidechain‐Mediated Microphase Separation

AbstractStiffness‐variable polymers have found their enormous potential in practical applications that require automatic adaptation and modulation. However, prevailing materials are often constrained by specific operational triggers, limited mechanical responsiveness, and inadequate universality. In this study, drawing inspiration from the mechanism of non‐solvent induced phase separation (NIPS), a novel series of polymers exhibiting reversible water‐triggered stiffening is designed and synthesized by covalently incorporating poly(ethylene glycol) (PEG) as a non‐solvent mediator onto the hydrophobic poly(meth)acrylates backbones. Owing to the hydrophilicity difference between PEG sidechains and backbones, these polymers display swift and substantial alterations in stiffness, with large‐scale and regulable changes (from several‐fold to exceeding 200‐fold) upon water penetration, resulting from water‐induced microphase separation. Meanwhile, the polymers also possess intrinsic dual‐responsive shape‐memory properties. Due to the excellent commercial availability, versatility, and designability of these polymers, the work provides novel perspectives for the advancement of water‐triggered stiffening materials and opens avenues for their prospective applications in various domains.

Functional biocarbon-based coatings for wood protection and indoor air depollution

Growing concerns about indoor air pollution heighten the need to develop depolluting materials to achieve a healthy built environment. This study developed functional coatings for wooden surfaces using 20 wt% photocatalytic biocarbon particles doped with manganese oxide (BC–MnO2) and two different coating materials (linseed oil and waterborne acrylic). The samples' surface hydrophobicity and color properties were tested before and after accelerated aging. The depolluting potential of the samples was evaluated by formaldehyde removal efficiency test in indoor conditions. Results showed that adding BC-MnO2 particles increased the hydrophobicity regardless of the coating material's type. After accelerated aging, the hydrophobicity of all samples increased, which was attributed to the curing of the oil and acrylic polymers and the increase in surface roughness eventually caused by surface damage. The color change (ΔE) was more intense in the case of uncoated wood and samples without BC-MnO2. However, the BC-MnO2-containing coatings were effective in color preservation (ΔE < 2), which was attributed to the anti-UV property of biocarbon. The BC-MnO2-containing coatings exhibited a promising formaldehyde removal efficiency of up to 24 % and 46 % for oil and acrylic samples, respectively. The combination of BC-MnO2 and acrylic material was more favourable to attracting the formaldehyde molecules, likely due to the similar polarity. The developed functional coatings exhibited an acceptable ability for wood protection and formaldehyde remediation and can be potentially used to enhance indoor air quality.

Synthesis and Characterization of Novel Terpolymers as Viscosity Index Improvers Using Industrial Waste for Iraqi Lubricating Oil

The potential utilization of industrial waste, specifically polyethylene wax, to enhance the efficiency of alkyl acrylate polymers as viscosity index improver (VII) additives in lubricating compositions has been investigated. Four terpolymers (w1, w2, w3, and w4) were synthesized via free radical polymerization, incorporating hexyl acrylate, 1-tetradecene, and industrial waste-sourced polyethylene wax at varying molar ratios. These terpolymers were characterized through gel permeation chromatography (GPC) for molecular weight determination, Fourier transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance (1H-NMR) spectroscopy for chemical structure analysis, and thermal gravimetric analysis (TGA) for thermal stability assessment. The study evaluated the efficiency of these terpolymers as viscosity index improvers (VII) in combination with free additives Iraqi lubricating oil (base oil 60). Our results demonstrate the feasibility of significantly enhancing the efficiency of viscosity improvers through the utilization of industrial waste, with improvements proportional to terpolymer concentration. The terpolymer w3, characterized by a balanced molar ratio of 1:1:1, exhibiting the highest degree of efficacy, which gave VI of 206 at 5 wt.% concentration compared with free additive lubricating oil, which gives VI of 98. This study offers promising insights into the sustainable use of industrial waste to improve lubricating compositions.

An Application of Self-Healing Clear Coat

The self-healing concept for an acrylic polymer was investigated. In the study, the self-healing performance of the developed varnish was examined. Varnish used; It is a two-component, solvent-based, hydroxylated acrylic resin-based varnish. An isocyanate-based hardener was used as the second component.To demonstrate self-healing performance; Varnish mixed with hardener and thinner in appropriate mixing ratio was applied to the surface with a spray gun. Deformation was created on the varnish, which was cured at 80°C for 30 minutes, and the self-healing performance of this deformation was monitored by gloss measurements.At the end of the study, it was determined that the varnish developed could self-heal at a rate of 90%.

Influence of amine surface treatments of carbon nanotube and boron nitride hybrid fillers on the thermal and mechanical properties of flexible amine‐based acrylate composites via 3D vat photopolymerization

AbstractOwing to the rapid advancement in electronic devices, thermal interface materials have been introduced to solve the thermal dissipation and electrical insulation problems in electronic parts and packaging materials. In this study, flexible thermally conductive acrylate‐based composites were fabricated via 3D vat photopolymerization. The effects of amine functional groups on the thermal and mechanical properties of acrylate polymers were explored. Surface‐treatment agents, namely, (3‐aminopropyl)triethoxysilane (APTES) and octadecylamine (ODA), were selected to enhance the poor dispersibility of fillers in the resin matrix caused by aggregation. The APTES‐treated carbon nanotube (CNT)–boron nitride (BN) hybrid composite exhibited the highest thermal conductivity of 0.990 W m−1 K−1, which was remarkably 482.35% higher than that of the matrix owing to the addition of 30 wt% BN, 0.5 wt% CNTs, and APTES treatment. The ODA‐treated CNT composite, which contained only 0.5 wt% CNTs, exhibited a thermal conductivity of 0.540 W m−1 K−1, which was 217.65% higher than that of the matrix. The electrical insulation properties of the composites were characterized, and the composites exhibited low electrical conductivity as electrical insulation materials. The advantages of the 3D‐printed flexible thermally conductive acrylate polymers usher in a new era of using polymer composites to address heat dissipation problems in complex structures.

Hydrophilic Poly(meth)acrylates by Controlled Radical Branching Polymerization: Hyperbranching and Fragmentation.

Topology significantly impacts polymer properties and applications. Hyperbranched polymers (HBPs) synthesized via atom transfer radical polymerization (ATRP) using inimers typically exhibit broad molecular weight distributions and limited control over branching. Alternatively, copolymerization of inibramers (IB), such as α-chloro/bromo acrylates with vinyl monomers, yields HBPs with precise and uniform branching. Herein, we described the synthesis of hydrophilic HB polyacrylates in water by copolymerizing a water-soluble IB, oligo(ethylene oxide) methyl ether 2-bromoacrylate (OEOBA), with various hydrophilic acrylate comonomers. Visible-light-mediated controlled radical branching polymerization (CRBP) with dual catalysis using eosin Y (EY) and copper complexes resulted in HBPs with various molecular weights (M n = 38 000 to 170 000) and degrees of branching (2%-24%). Furthermore, the optimized conditions enabled the successful application of the OEOBA to synthesize linear-hyperbranched block copolymers and hyperbranched polymer protein hybrids (HB-PPH), demonstrating its potential to advance the synthesis of complex macromolecular architecture under environmentally benign conditions. Copolymerization of hydrophilic methacrylate monomer, oligo(ethylene oxide) methyl ether methacrylate (OEOMA500), and inibramer OEOBA was accompanied by fragmentation via β-carbon C-C bond scission and subsequent growth of polymer chains from the fragments. Furthermore, computational studies investigating the fragmentation depending on the IB and comonomer structure supported the experimental observations. This work expands the toolkit of water-soluble inibramers for CRBP and highlights the critical influence of the inibramer structure on reaction outcomes.

Synthesis of Ag@SiO2 core-shell nanoparticles for antibacterial application in water-based acrylic polymer coatings

In this study, Ag@SiO2 core-shell nanoparticles were synthesized using the Stöber method and then physically mixing with MPS functionalized poly (styrene-co-acrylate) (PSA) emulsion to obtain a novel antibacterial composite material (PSA/Ag@SiO2). The dispersion of composite latexes was improved by the formation of Si-O-Si covalent bonds, and the migration of AgNPs on the surface of composite films enhanced their antimicrobial activity. Analysis of UV-Vis absorption spectra, TEM images, XPS and XRD data confirmed the core-shell structure of Ag@SiO2 and the successful coating of AgNPs by SiO2. TEM micrographs showed that Ag@SiO2 core-shell nanoparticles were uniformly dispersed in the composite latexes, with an average particle size of 198 nm for PSA/Ag@SiO2 composite latexes, larger than that of PSA latexes (162 nm). FTIR spectra also indicated the presence of Si-O-Si covalent bonds resulting from the sol-gel reaction between MPS functionalized PSA with Ag@SiO2. XPS and WCA characterization revealed the disruption of the core-shell structure of Ag@SiO2, leading to the migration of AgNPs to the air-film interface. The results of antibacterial activity demonstrated that PSA/Ag@SiO2 composite films displayed antibacterial activity against both E. coli and S. aureus, and the former displayer a slightly better antibacterial activity than the latter. The water-based acrylic polymer coatings with antibacterial properties explored in current work have various applications in wood paints, varnishes, metal protection, decorative systems and other related fields.

Structural properties controlled magnetisation of Ni/Al multilayers sputtered on flexible polymer substrate: Impact of Ni deposition rates

The goal of this work is to determine how the rate of Ni deposition rates affect the structural characteristics that regulate the magnetization of Ni/Al multilayer thin films sputtered on flexible acrylic acetate polymer substrates. The films with a 5[Ni(20 nm)/Al(10 nm)] structure were gradually sputtered as different Ni deposition rates in the total thickness of 150 nm. With an increase in the rate of Ni deposition, the Ni contents increased from 61.5% to 69.6%. And, X-ray diffraction analysis verified that the films featured a face-centered cubic structure with variable peak intensities. Also, the scanning electron microscopy surface morphology analyses revealed that variations in the film surfaces were a result of the deposition rates. For magnetic measurements, the differences in the structural analysis were observed to cause a notable variation in saturation magnetization, MS, and coercivity, HC values. Accordingly, MS values increased consistently between 359.0 and 389.7 emu cm−3, but HC values decreased from around 34–32 to 28 Oe with the increase in Ni deposition rate from 0.02 to 0.10 nm s−1. It is also observed that when the Ni layers are generated at very fast deposition rates, the Ni/Al multilayer films have a high MS/HC ratio, which is significant for magnetic sensors. It has been concluded that the magnetisation of Ni/Al multilayer thin films can be controlled by the structural properties adjusting the Ni deposition rate.

One-Stone-for-Two-Birds Method to Improve the SnO2 Layers for High Power-per-Weight Flexible Perovskite Solar Cell Mini-modules.

Maintaining the power conversion efficiency (PCE) of flexible perovskite solar cells (fPSCs) while decreasing their weight is essential to utilize their lightweight and flexibility as much as possible for commercialization. Strengthening the interfaces between functional layers, such as flexible substrates, charge transport layers, and perovskite active layers, is critical to addressing the issue. Herein, we propose a feasible and one-stone-for-two-birds method to improve the electron transport layer (ETL), SnO2, and the interface between the ETL and perovskite layer simultaneously. In detail, poly(acrylate ammonium) (PAAm), a low-cost polymer with a long chain structure, is added into the SnO2 aqueous solution to reduce the aggregation of SnO2 nanoparticles, resulting in the deposition of a conformal and high-quality ETL film on the tin-doped indium oxide film surface. Simultaneously, PAAm addition can effectively regulate the crystallization of the perovskite films, strengthening the interface between the SnO2 film and the buried surface of the perovskite layer. The outstanding PCEs of 22.41% on small-scale fPSCs and 18.54% on fPSC mini-modules are among the state-of-the-art n-i-p type fPSCs. Moreover, the fPSC mini-module on the 20 μm-thick flexible substrate shows a comparable PCE with that of the fPSC mini-module on the 125 μm-thick flexible substrate, exhibiting a high power-to-weight of 5.097 W/g. This work provides an easy but essential direction for further applications of fPSCs in diverse scenarios.

A comparative and experimental study to evaluate the use of nanocontainer solutions for removing polymeric coatingsfrom glass artifacts

Purpose The purpose of this study is to evaluate the effectiveness of nanocontainer solutions in removing deteriorated and aged polymers commonly used in coating and consolidating archaeological glass. Design/methodology/approach This study focused on characterizing glass surfaces coated with two commonly used polymeric materials in archaeological glass preservation. Furthermore, the study evaluates the elimination of these coatings from the surfaces by using innovative aqueous systems composed of micellar solutions (MS) and oil-in-water (O/W) Texapon-P microemulsions (TEX). Glass samples coated with selected polymers were subjected to thermal and photochemical aging to simulate natural degradation conditions. This study aimed to evaluate the effectiveness of nanocontainer aqueous systems compared to acetone (Ac), a conventional solvent commonly used for removal procedures. The characterization procedures involved transmission electron microscopy, USB digital microscopy, scanning electron microscopy, color alteration and gravimetric measurement. Findings The findings indicate that the effectiveness of novel techniques using aqueous nanocontainer systems is quite promising when considering a “green approach” to preserving cultural heritage. Microscopic examination demonstrated the efficacy of MS in effectively removing acrylic and vinyl polymers from the glass surface. Furthermore, TEX proved effective in removing polyvinyl acetate (PVA) over Paraloid B72 (B-72). In addition, the measurement of color alteration values revealed a decrease after using MS compared to the standard sample before applying the polymers, with values of ΔE = 1.48 and 1.82 for B-72 polymer and PVA, respectively. Originality/value This research provides nanocontainer solutions for removing aged polymers from the glass surface. This makes the current study a promising step for treating archaeological glass.

ИЗУЧЕНИЕ ПРОЦЕССОВ КОМПЛЕКСООБРАЗОВАНИЯ В ПОЛИМЕРНЫХ БИОДЕГРАДИРУЕМЫХ КОМПОЗИЦИЯХ

One of the possible directions of the development of targeted substance delivery systems is the creation and introduction of biodegradable polymers into production. Their distinctive feature is that they are capable of spontaneously gradually degradation in the body due to natural biochemical processes. There is an increasing spread pharmaceutical form, which use similar excipients in their technology – medicinal ocular insert. Modified cellulose, gums and rare-cross-linked acrylic polymers are used to create a biodegradable matrix base. In terms of development approach, ocular inserts can be divided into two groups according to the principle of matrix biodegradation. In non-biodegradable composites, the effect of prolongation of the therapeutic effect is observed due to the release of the active substance from the non-decomposing matrix. This fact can be confirmed by both pharmacopoeial and non-pharmacopoeial methods. The classic tests regulated by the Pharmacopoeia of the XV edition include the "Dissolution" test (GPM.1.4.2.0014 "Dissolution of solid pharmaceutical dose forms"), and for non–pharmacopoeial ones – dialysis through a semipermeable membrane according to Kruvchinsky or using Franz's dialysis cells. The analysis of the kinetics of dissolution helps to determine and select the most suitable matrix-forming agent to be used in the composition with other substances in the composition of ocular insert. Ocular inserts with a biodegradable matrix have a second factor that affects the release of active substances – the formation of complexes or associates between parts of the matrix and the active ingredient molecules. These intermolecular compounds can indirectly prolong the effect of the drug. All features must be taken into account in the development of ocular inserts, since they, among other things, help to model fundamentally new ways of targeted delivery of substances. In this case, it is necessary to develop a test for the second modified release factor, which would reliably determine the presence of complexation processes within the selected ocular inserts model.

Experimental study and multi‐scale refinement model of high damping acrylic polymer matrix VEDs for civil structural seismic retrofit

AbstractThe viscoelastic dampers (VEDs), which can provide both stiffness and damping, have been recently introduced into the field of structural vibration control for seismic enhancement of civil engineering structures. In this study, a kind of high damping acrylic polymer matrix VEDs (HDPVED) is developed independently, and this innovative HDPVED can solve the significant problem of service performance under medium‐high temperature environments, as well as low‐frequency vibration control under earthquake actions for civil engineering structures. To systematically investigate the influencing rules of frequency, temperature, and displacement amplitude on the mechanical properties and damping dissipation performance of HDPVEDs, a series of dynamic mechanical performance tests of the developed HDPVEDs are carried out at different frequencies, temperatures, and displacement amplitudes. The research results show that HDPVED exhibits excellent damping dissipation capability and adaptability under medium‐high temperature environments and low‐frequency excitations. The mechanical properties and energy dissipation performance present a strong correlation with frequency, temperature and displacement amplitude, and there is an obvious coupling effect between the three influencing factors. Based on the macroscopic mechanical property research of HDPVED, the microscopic damping mechanism and microscopic mechanical properties of HDPVED are then investigated. High‐order fractional derivative fraction Voigt and Maxwell model in parallel (FVMP) models are preferred to characterize the combined hyper‐elasticity and viscoelasticity owned by networked molecular chains and free molecular chains. The breaking and reconstruction theory of microphysical bonds is used to assess the effect of packing particles, and the time‐temperature equivalence principle is introduced to assess the effect of temperature. The multi‐scale refinement model is proposed, and the validity and accuracy of this model are verified by testing data of HDPVED. The study results show that the proposed model can accurately describe the effects of frequency, temperature, displacement amplitude, and microstructure on the multi‐scale mechanical properties of HDPVED. It provides a theoretical basis for the multi‐scale design and development of high damping VEDs.

Preparation of high‐barrier performance paper‐based materials from biomass‐based silicone‐modified acrylic polymer emulsion

AbstractHigh‐barrier performance, especially under extreme working conditions, is the key to replacing other types of packaging materials with paper‐based materials. In this paper, two biomass‐based polymers, sodium alginate (SA), and chitosan, were used to form a barrier coating with silicone emulsions to prepare a high‐performance paper‐based barrier material. By double coating, the water and oilproof functions were superimposed. The two prepared coated papers were characterized by infrared spectroscopy analysis, contact angle test, and scanning electron microscopy analysis, while their water resistance, oil resistance, thermal oil resistance, and thermal stability were tested. The water and oil repellency were achieved by double coating. The Cobb value of the chitosan‐silicone emulsion‐coated paper reached 5.3 g/m2, with a Kit grade of Level 12, and could block the penetration of castor oil at 80°C within 24 h. The Cobb value of the sodium alginate‐silicone emulsion‐coated paper was 41.6 g/m2, much higher than that of the uncoated paper, with a Kit grade of up to Level 10, which could slow down the rate of castor oil penetration at 80°C within 24 h. The test results showed that there was no chemical reaction between the paper‐based coatings, and the coated paper surface had good film formation, while the double coating method increased the thermal decomposition temperature of the overall barrier coating, effectively improving the thermal stability of the coating and achieving high‐barrier performance at lower cost and under extreme working conditions.Highlights Water and oil resistance under extreme operating conditions. High‐performance paper‐based barrier materials. Dual‐layer coating method for water and oil repellency. High‐barrier performance at lower cost. Excellent hot oil resistance and thermal stability.

Green disposal of waste smartphone protective film: Efficiency, mechanism, bench-scale test and secondary waste reutilization

The manufacture and obsolescence of smartphones produce numerous waste plastic accessories (e.g., waste smartphone protective film (WSPF)), possessing immense potential for recycling. However, available recycling technologies have limitations such as substrate damage and secondary pollutant generation. The present study aimed to develop a green disposal method that not only recycled polyethylene terephthalate (PET) from WSPF, but also reused the stripped polyacrylate (PAA) adhesive as an adsorbent to reduce solid waste generation. When the WSPF was treated in 1 mol/L NaOH solution at 90 °C, the PAA hydrolyzed to two main by-products of 1-butanol and 2-ethylhexanol, weakening the binding strength between PAA and PET and then efficient separation of them. Further bench-scale test revealed that over 97.2% of detachment efficiency toward PAA was achieved during continuous treatment of 17 batches of WSPF (200 g for each) without supplement of NaOH and generation of wastewater. Meanwhile, the economic evaluation indicated that the recycling method would generate a net profit margin of 647% for the second year without considering the incurrence of new cost and input. Additionally, the pyrolysis of waste PAA enabled its conversion into potential adsorbent, which showed 2 to 4 times enhanced adsorption capacity toward styrene and ethyl acetate after modification with NaOH solution. This study provides a green method for recycling waste plastics and inspires a referable solution for solid waste treatment in the smartphone industry.

Design and Analysis of Composite Biomaterial Bone Graft Plate

The mixing technique was applied in this study to enhance the strength performance of the cement. The addition of 3% by weight of hydroxyapatite (HA) nanoparticles were mixed with 97% polymethyl methacrylate (PMMA) acrylic polymer, which has a nano size to serve as the matrix material. The surface roughness and continuous porosity of the bone cement were found to be slightly increased by the incorporation of nanoparticles, which enhanced bone-implant osseointegration and ingrowth. Atomic force microscopy (AFM) analysis revealed that the addition of hydroxyapatite (HAp) nanoparticles resulted in a surface roughness value (Sa) of 16.25 nm, which is similar to that of natural bone. The energy-dispersive X-ray spectroscopy (EDS) mapping results discover precentor material and uniform distribution. The Sample exhibited promising results in the antibacterial test, showing efficacy against bacteria both with and without sterilization, confirming its antibacterial properties. The mechanical tests conducted on the sample, including tensile, compression, bending and Vickers hardness tests, yielded favorable results and indicated that the sample is suitable for its intended application. In the theoretical works the design of the bone, screw, and bone plate was conducted using SolidWorks, followed by an analysis using ANSYS under both axial and bending load conditions. The theoretical analysis revealed that the safety factor was less than 1 when an axial load of 13 N was applied and a bending load of 2 N was applied, indicating that the structure may not be able to withstand these loads safely. Under both ambient and physiologically relevant conditions in the human body, HA and PMMA have demonstrated to be excellent choices for enhancing the clinical performance of bone cement. This, in turn, can lead to increased longevity of implants, decreased patient risk, and lower healthcare costs