Polymerization Of Methacrylate Research Articles

Arginine-Functional Methacrylic Block Copolymer Nanoparticles: Synthesis, Characterization, and Adsorption onto a Model Planar Substrate.

Recently, we reported the synthesis of a hydrophilic aldehyde-functional methacrylic polymer (Angew. Chem., 2021, 60, 12032-12037). Herein we demonstrate that such polymers can be reacted with arginine in aqueous solution to produce arginine-functional methacrylic polymers without recourse to protecting group chemistry. Careful control of the solution pH is essential to ensure regioselective imine bond formation; subsequent reductive amination leads to a hydrolytically stable amide linkage. This new protocol was used to prepare a series of arginine-functionalized diblock copolymer nanoparticles of varying size via polymerization-induced self-assembly in aqueous media. Adsorption of these cationic nanoparticles onto silica was monitored using a quartz crystal microbalance. Strong electrostatic adsorption occurred at pH 7 (Γ = 14.7 mg m-2), whereas much weaker adsorption occurred at pH 3 (Γ = 1.9 mg m-2). These findings were corroborated by electron microscopy, which indicated a surface coverage of 42% at pH 7 but only 5% at pH 3.

Polymer Passivated All Inorganic Micro‐Structured CsPbIxBry Perovskite Toward Highly Efficient Photodetectors

AbstractSolution‐processed inorganic perovskites cause chemical and structural defects unfavorable for photodetector application. Using a binary solvent, defects in CsPbIxBry (CPIB) perovskite are passivated with poly 4‐vinylpyridine (PVP) and Poly methyl methacrylate (PMMA) polymers. X‐ray photoelectron spectroscopy and FTIR spectra reveal a Lewis base‐acid interaction between Pb2+ and polymer, confirming the passivation of CPIB perovskite. Scanning electron microscopy analysis shows a dual‐surface morphology with microribbons and microcrystals in perovskites. After PMMA treatment, CPIB perovskite exhibits a blue shift in the bandgap (1.8 to 1.95 eV), while the PVP induced a redshift, reducing the bandgap to 1.7 eV. Blue shift in PL analysis indicates modification of grain boundaries. A higher lifetime obtained for CPIB/PVP confirms the restraint of non‐radiative recombinations. Photodetectors are fabricated with pristine CPIB, CPIB/PVP, and CPIB/PMMA perovskites. The passivated CPIB/PVP‐based photodetector exhibits a quick rise time of ≈23 ms and a decay time of ≈17 ms. It also demonstrates a remarkable photoresponsivity of 23 mA W−1, an internal quantum efficiency of 4.9%, and a detectivity of 15.0 × 1010 Jones at 10 mW cm−2 light intensity. This approach shows the potential for environmentally stable polymers to passivate inorganic perovskites for high photodetection performance.

Oil absorbent based on lauryl methacrylate grafting onto cellulose of water hyacinth (Eichhornia crassipes)

AbstractIn this article, a novel oil‐absorbent polymer was synthesized by graft polymerization of lauryl methacrylate (LMA) onto water hyacinth (WH) using 2,2′‐azobisisobutyronitrile (AIBN) as initiator and divinyl benzene (DVB) as a crosslinking agent. The effects of initiator content, LMA content, reaction temperature, reaction time, and crosslinker content on the superabsorbent polymer were investigated. The prepared graft copolymer WH‐g‐LMA was analyzed using FTIR, SEM, XRD, and TGA. In the presence of the better cross‐linker DVB (1.5%) and contact time of about 25 min, the maximal Q (oil sorption capacity) of co‐polymer towards crude and Soybean oils is 23.68 and 25.72 g g−1, respectively. The Q is reduced when sorbent dosage increased, but it increases with increasing the temperature and reaches a maximum of 40 °C. The reusability of co‐polymer is characteristic of 7 sorption/desorption cycles.

A Single-Component Janus Zwitterionic Hydrogel Patch with a Bionic Microstructure for Postoperative Adhesion Prevention.

The development of anti-adhesion hydrogels for preventing postoperative adhesions is an ongoing challenge, particularly in achieving a balance between exceptional antifouling properties and effective in situ tissue retention. In this study, we propose a unique approach with the design of a single-component Janus zwitterionic hydrogel patch featuring a bionic microstructure. The Janus patches were prepared through free radical polymerization of sulfobetaine methacrylate with N, N'-methylenebis(2-propenamide) as the cross-linker. The incorporation of hexagonal facets separated by interconnecting grooves on one side imparts durable and reliable in situ retention capabilities to the Janus hydrogel patch when it is applied to traumatized tissues. The opposing flat surface exhibits outstanding resistance to bacteria, proteins, and cell adhesion, due to the superhydrophilicity and excellent antifouling characteristics of zwitterionic polymers. This dual functionality empowers the Janus hydrogel patch to mitigate adhesions between traumatized and surrounding tissues. The hexagonal and groove bionic microstructures facilitate rapid drainage, promoting swift contact with the tissue for increased adhesion strength, while independent hexagonal microfacets enhance the peeling energy. In an in vivo setting, Janus zwitterionic hydrogel patches with surface microstructures form mutually embedded structures with the cecum surface, minimizing the likelihood of slippage and detachment. Remarkably, in vivo experiments involving abdominal wall cecum injuries illustrate the Janus zwitterionic hydrogel patch's superior anti-adhesion effectiveness compared to commercial controls. Thus, the Janus hydrogel patch, distinguished by its bionic microstructure surface, presents substantial potential in the biomedical field for averting postoperative adhesions.

Selective solid phase extraction of phototoxic furanocoumarins using molecularly imprinted polymers

Furanocoumarins are secondary plant metabolites found in citrus plants. Essential oils from these plants are widely used in cosmetic products. They have attracted attention for their phototoxicity, which can even lead to skin burns. Therefore, the furanocoumarin concentration is controlled by the European Union according to Regulation (EC) No. 1223/2009, where a limit of 1 mg kg−1 is specified in sun protection and bronzing agents. This study describes the synthesis of two molecularly imprinted polymers (methacrylamide and methacrylic acid as monomers) as novel materials for solid phase extraction. After optimisation of the extraction protocol, both polymers gave satisfying recovery results for a furanocoumarin standard mixture containing the six markers proposed by the International Fragrance Association (IFRA). Furthermore, spiked sun oil samples were extracted using an adapted extraction protocol. Since the studies showed promising results including 75–149 % recovery and 100 % loading efficiency for the methacrylic acid polymer, a validation of the analytical method was performed. Analysis was performed using HPLC-MS/MS in high specificity multi-reaction monitoring mode. The validation showed acceptable results for most parameters. In addition, a comparison with commercially available Strata-X cartridges was completed, revealing superior recovery performance of the molecularly imprinted polymer. In conclusion, molecularly imprinted polymers represent a novel and efficient method for selective solid-phase extraction of phototoxic furanocoumarins.

One-pot Formulation of Cationic Oligochitosan Coated Nanoparticles via Photo- Polymerization Induced Self-Assembly.

During last few decades, oligochitosan (OCS)-coated nanoparticles have received great interest for nanomedicine, food and environment applications. However, their current formulation techniques are time-consuming with multi-synthesis/purification steps and sometimes require the use of organic solvents, crosslinkers and surfactants. Herein, we report a facile and rapid one-pot synthesis of OCS-based nanoparticles using photo-initiated reversible addition fragmentation chain transfer polymerization-induced self-assembly (Photo-RAFT PISA) under UV-irradiation at room temperature. To achieve this, OCS was first functionalized by a chain transfer agent (CTA) resulting in a macromolecular chain transfer agent (OCS-CTA), which will act as a reactive electrostatic/steric stabilizer. Owing to its UV-sensitivity, OCS-CTA was then used as photo-iniferter to initiate the polymerization of 2-hydroxypropyl methacrylate (HPMA) in aqueous acidic buffer, resulting in OCS-g-PHPMA amphiphilic grafted copolymers which self-assemble into nano-objects. Transmission electron microscopy and light scattering analysis reveal formation of spherical nanostructures.

Self-Catalyzed Hydrolysis of Nitrile-Containing RAFT Chain-Transfer Agent and Its Impact upon Polymerization Control of Methacrylic Monomers.

Self-catalyzed hydrolysis upon storage of the common RAFT chain-transfer agent (CTA) 4-cyano-4-[(thiothiopropyl)sulfanyl] pentanoic acid (CTPPA) is confirmed, where the nitrile group is transformed into an amide by catalysis from the adjacent carboxylic acid moiety. The amide-CTA (APP) is found to poorly control molecular weight evolution during polymerization of two methacrylates, methyl methacrylate (MMA) and N,N-(dimethylamino)ethyl methacrylate (DMAEMA), likely due to poor reinitiation speed in the pre-equilibrium. However, when attached to a macromolecule, the impact of this amide moiety becomes insignificant and chain extension proceeds as expected with CTPPA. In light of CTPPA and similarly hydrolyzable CTAs being extensively employed for aqueous polymerizations of methacrylates, these findings highlight the importance of CTA purity when performing RAFT polymerizations.

Pyrazole-based photoinitiator with antibacterial activity

1-(naphthalen-2-yl)-2-(1H-pyrazol-1-yl) ethanone (MPPY) was synthesized. The structure was characterized by spectral analysis (1H-NMR, FTIR). The molar  absorptivity of MPPY is high enough, similarly to acetonaphthone derivatives, to be used as an efficient type I photoinitiator. The influence of MPPY concentration and the addition of the co-initiator N-methyldiethanolamine (MDEA) on methyl methacrylate (MMA) polymerization were also investigated.  Additionally, MPPY showed good antibacterialactivity against Escherichia coli and Staphylococcus aureus (diffusion method).

An Electrode-Crosstalk-Suppressing Smart Polymer Electrolyte for High Safety Lithium-Ion Batteries.

Electrode crosstalk between anode and cathode at elevated temperatures has been identified as a real culprit triggering the thermal runaway of lithium-ion batteries. Herein, to address this challenge, a novel smart polymer electrolyte is prepared through in-situ polymerization of methyl methacrylate and acrylic anhydride monomers within a succinonitrile-based dual-anion deep eutectic solvent. Owing to the abundant active unsaturated double bonds on the as-obtained polymer matrix end, this smart polymer electrolyte can spontaneously form a dense crosslinked polymer network under elevated temperatures, effectively slowing down the crosstalk diffusion kinetics of lithium ions and active gases. Impressively, LiCoO2/graphite pouch cells employing this smart polymer electrolyte demonstrate no thermal runaway even at the temperature up to 250°C via accelerating rate calorimeter testing. Meanwhile, because of its abundance of functional motifs, this smart polymer electrolyte can facilitate the formation of stable and thermally robust electrode/electrolyte interface on both electrodes, ensuring the long cycle life and high safety of LIBs. In specific, this smart polymer electrolyte endows 1.1 Ah LiCoO2/graphite pouch cell with a capacity retention of 96% after 398 cycles at 0.2 C. This article is protected by copyright. All rights reserved.

Fast-polymerized lubricant and antibacterial hydrogel coatings for medical catheters

Medical catheters are highly susceptible to friction and infection when intervening or implanting in the body, and to thrombosis when in contact with blood. Coating medical catheters with lubricant and antibacterial hydrogel is an effective strategy but struggle to achieve. Here, hydrogel coating on the catheter surface with lubrication and antibacterial properties was constructed by the rapid polymerization of acrylamide (AAM) and sulfobetaine methacrylate (SBMA) in the presence of quaternary ammonium chitosan (QCS) based on the redox-based cross-linking method. First, the medical catheter surface was decorated with a polyethyleneimine (PEI) adhesive layer. The pre-gel solution was then applied to the catheter surface, followed by immersion in an aqueous FeSO4·7H2O solution, where a large amount of SO4-• was generated by a redox reaction between ammonium persulfate (APS) and Fe2+, which rapidly triggered the monomer to cross-link to form the coating. Polyelectrolyte PEI as the adhesive layer could bind the coating to the substrate through hydrogen bonding interactions and confer antimicrobial properties to the coating with the assistance of QCS (antibacterial rate of 95.88 % against E. coli and 97.11 % against B. subtilis). The hydrogel coatings exhibited outstanding lubricity with a low coefficient of friction (COF ≈ 0.053) and excellent antifouling properties (resists non-specific protein adsorption, inhibits platelet adhesion and prevents thrombosis (The clotting time was extended from 25.6 s to 74.7 s)) based on the integration of SBMA. This work shed new light on the design of hydrogel coatings to achieve modification of the substrate surface.

Penggabungan Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> dalam Matriks Poli (Metil Metakrilat) untuk Aplikasi Memori Tidak Meruap

MXenes, with their unique surface properties and 2D structure, have demonstrated promising potential in electronic devices, particularly in memory storage. This study explored the potential of 2D Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> for the nonvolatile memory (NVM) application. The simple solution process routes were used to fabricate the two-terminal bistable switching devices. The silver nanowires/nanocomposite/ITO structure was deposited on a glass substrate using spin coating and spray coating techniques. The Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene flakes were incorporated into a poly(methyl methacrylate) (PMMA) polymer host to form the nanocomposite and act as a charge-trapping layer. Meanwhile, PMMA acts as a dielectric layer. The measured current-voltage data showed a bistable current behavior with the presence of a memory window. The fabricated NVM memory devices were reprogrammable when the endurance test was performed and stable up to 1×104 s cycles with a distinct ON/OFF ratio of 103. The conduction mechanisms were identified using the curve-fitting method with double log plots of current-voltage (I-V) data. Based on the obtained I-V characteristics, various conduction mechanisms, especially Schottky and Poole-Frenkel emission, trapped charge limiting current, and space charge limited current, were proposed to be responsible for the bistable switching behavior. Thus, the results of this study provide an experimental basis for using MXene in non-volatile memory applications.

Facile Synthesis of Poly(methyl methacrylate) Silica Nanocomposite Monolith by In Situ Free Radical Polymerization of Methyl Methacrylate in the Presence of Functionalized Silica Nanoparticles.

Novel porous poly(methyl methacrylate) (PMMA) silica nanocomposites have been produced by utilization of polymerization-induced phase separation in a simple one-pot approach. A facile free radical polymerization of MMA in the presence of surface methacrylate-functionalized silica nanoparticles was carried out in ethanol-based solvents, successfully producing novel, morphologically designable porous nanocomposite monoliths. Differing from standard free radical polymerization in solution, a mixture of good and poor solvents (ethanol/N,N-dimethylformamide ratio) for the resulting polymer was used to trigger spinodal phase separation. The influence of monomer concentration, as well as solvent composition, on the morphology of the resulting porous polymers has been investigated. Porous monolith structures composed of connected particles and co-continuous morphologies were observed under a scanning electron microscope depending on the polymerization conditions. The resulting polymers were insoluble and showed swelling characteristics in some organic solvents that are capable of dissolving regular PMMA, indicating covalent bonds between the functionalized silica nanoparticles and the polymer chains. The presence of silica particles in the final polymer was proven via an ATR-IR analysis. The glass transition temperature of the present PMMA-silica nanocomposite was higher than that of the conventional PMMA. The porous polymer immersed in a mixed organic solvent showed coloration induced by the Christiansen effect.

Synthesis and characterization of graft copolymer hydrogel by “grafting from” atom transfer radical polymerization using brominated macro monomeric initiator and investigation of hydrogel properties

AbstractIn this study, poly(ɛ-caprolactone-g-2-hydroxy ethyl methacrylate) [P(CL-g-HEMA)] graft copolymer hydrogels were successfully synthesized through multi-step reactions. For this purpose, firstly, hydroxyl-terminated poly(ɛ-caprolactone) (PCL-OH) was obtained by ring-opening polymerization (ROP) method of ɛ-caprolactone using 3-chlor-1,2-propanediol initiator, which is suitable for ring-opening polymerization method. Then, from the reaction of synthesized PCL-OH and 3-bromopropionyl chloride, a new brominated poly(ɛ-caprolactone) (PCL-Br) was synthesized for use as a functionalized atom transfer radical polymerization (ATRP) initiator. Poly(ɛ-caprolactone-g-2-hydroxy ethyl methacrylate) [P(CL-g-HEMA)] graft copolymer hydrogels were synthesized by “grafting from” atom transfer radical polymerization (ATRP) of 2-hydroxy ethyl methacrylate (HEMA) presence the new synthesized functionalized ATRP initiator (PCL-Br) and hydrogel properties were investigated. The synthesized functionalized initiators and graft copolymer hydrogel were characterized by spectroscopic methods such as 1H-NMR, FT-IR, TGA, DSC and SEM. The observation of two different decomposition temperatures, respectively, from the TGA analysis results may support the formation of the biblock graft copolymer. A glass transition temperature (Tg) of the graft copolymer hydrogel was found by DSC, and this value is between the Tg values of the homopolymers forming the graft copolymer hydrogel. Water swelling values of graft copolymer hydrogels were measured and calculated every 24 h in pure water with pH = 7 at from + 4 to 65 °C. Considering the weight of dry graft copolymer hydrogels, it was seen that water was absorbed at most at + 4 °C. As the temperature increased, the water absorption or swelling of the hydrogel decreased.

Constructing the Polymer Molecules to Regulate the Electrode/Electrolyte Interface to Enhance Lithium-Metal Battery Performance.

Lithium-ion batteries, with high energy density and long cycle life, have become the battery of choice for most vehicles and portable electronic devices; however, energy density, safety and cycle life require further improvements. Single-functional group electrolyte additives are very limited in practical applications, a ternary polymer bifunctional electrolyte additive copolymer (acrylonitrile-butyl hexafluoro methacrylate- poly (ethylene glycol) methacrylate- methyl ether) (PMANHF) was synthesized by free radical polymerization of acrylonitrile, 2, 2, 3, 4, 4, 4-hexafluorobutyl methacrylate and poly (ethylene glycol) methyl ether methacrylate. A series of characterizations show that in Li metal anodes, the preferential reduction of PMANHF is conducive to the formation of a uniform and stable solid electrolyte interphase layer, and Li deposition is uniform and dense. At the NCM811 cathode, a film composed of LiF- and Li3N-rich is formed at the cathode-electrolyte interface, mitigating the side reaction at the interface. At 1.0 mA cm-2, the Li/Li cell can be stabilized for 1000 cycles. In addition, the Li/NCM811 cell can stabilize 200 cycles with a cathode capacity of 153.7 mAh g-1, with the capacity retention of 89.93 %, at a negative/positive capacity ratio of 2.5. This study brings to light essential ideas for the fabrication of additives for lithium-metal batteries.

Topology Controlled All‐(Meth)acrylic Thermoplastic Elastomers by Multi‐Functional Lewis Pairs‐Mediated Polymerization

AbstractIt remains challenging to synthesize all‐(meth)acrylic triblock thermoplastic elastomers (TPEs), due to the drastically different reactivities between the acrylates and methacrylates and inevitable occurrence of side reactions during polymerization of acrylates. By taking advantage of the easy structural modulation features of N‐heterocyclic olefins (NHOs), we design and synthesize strong nucleophilic tetraphenylethylene‐based NHOs varying in the number (i.e. mono‐, dual‐ and tetra−) of initiating functional groups. Its combination with bulky organoaluminum [iBuAl(BHT)2] (BHT=bis(2,6‐di‐tBu‐4‐methylphenoxy)) constructs Lewis pair (LP) to realize the living polymerization of both acrylates and methacrylates, furnishing polyacrylates with ultrahigh molecular weight (Mn up to 2174 kg ⋅ mol−1) within 4 min. Moreover, these NHO‐based LPs enable us to not only realize the control over the polymers’ topology (i.e. linear and star), but also achieve triblock star copolymers in one‐step manner. Mechanical studies reveal that the star triblock TPEs exhibit better mechanical properties (elongation at break up to 1863 % and tensile strength up to 19.1 MPa) in comparison with the linear analogs. Moreover, the presence of tetraphenylethylene group in the NHOs entitled the triblock TPEs with excellent AIE properties in both solution and solid state.

Surface modification of polytetrafluoroethylene (PTFE) fibers through methyl methacrylate (MMA) polymerization for self-lubricating composites

PTFE fibers exhibit strong inertia and possess restricted interfacial compatibility with resin, thereby constraining the application of PTFE self-lubricating composites. To address this issue, PTFE-g-MMA fibers were synthesized by grafting MMA onto the surface of PTFE fibers using high-energy irradiation and chemical grafting techniques, resulting in the enhancement of the tribological properties (the friction coefficient has been reduced by approximately 42.2% and the wear rate has been reduced by about 87.9%) and mechanical properties (the interlaminar shear strength (ILSS) experienced a substantial increase of approximately 45.8%) of the composites. The influence of grafting modification on the formation of PTFE transfer films and the effect of modification time on the tribological properties of composites were investigated systematically. The results indicated that graft modification disrupted the C–F bond of PTFE and promoted the formation of metal-chelated carboxylates, facilitating the formation of PTFE transfer films on the counter surface. This research could provide a general and feasible strategy for large-scale modification of PTFE fibers with exceptional comprehensive properties.

Synthesis and photo‐initiated radical polymerization of methacrylates derived from bio‐based ω‐hydroxycarboxylic acids

AbstractThe bio‐based methacrylates 9‐(methacryloyloxy)‐10,18‐dihydroxyoctadecanoic acid/9,18‐dihydroxy‐10‐(methacryloyloxy)octadecanoic acid isomer mixture and 22‐methacryloyloxydocosanoic acid were synthesized from 9,10‐epoxy‐18‐hydroxyoctadecanoic acid and 22‐hydroxydocosanoic acid. The white crystalline 9,10‐epoxy‐18‐hydroxyoctadecanoic acid and cream‐colored 22‐hydroxydocosanoic acid were isolated from both the bark of Betula pendula and cork of Quercus suber after extraction of the milled plant materials with methanol, treating the insoluble residues with 2‐propanole containing suspended sodium hydroxide, application of a working up procedure developed in this work for the resulting mixture, and purification of the products obtained. The new bio‐based methacrylates show higher reactivity in the photoinitiated polymerization in comparison with the commercial laurylmethacrylate as detected by photo‐differential scanning calorimetry (DSC). For comparison, traditional free radical polymerization of the new bio‐based methacrylates was carried out in dimethylsulfoxide using 2,2'‐azobis‐(2‐propionitrile) as initiator. Furthermore, the quantitative conversion of the bio‐based monomers during the photoinitiated polymerization makes these bio‐based monomers interesting for application in coatings. As expected, the photopolymer made from the 9‐(methacryloyloxy)‐10,18‐dihydroxyoctadecanoic acid/9,18‐dihydroxy‐10‐(methacryloyloxy)octadecanoic acid isomer mixture is amorphous. Interestingly, the photopolymer made from the 22‐methacryloyloxydocosanoic acid contains crystalline structures as detected by DSC investigation.

Multistep pH-peak-focusing liquid chromatography with a hydrophilic polymer gel column for separation of rare earth elements

Multistep pH-peak-focusing liquid chromatography with a column packed with a hydrophilic polymer gel (a cross-linked hydroxylated methacrylic polymer gel) was developed for separation of rare earth metal ions. Metal ions in a sample solution introduced to the column are chromatographically extracted into the stationary gel phase at the top of the column equilibrated with a basic solution used as the first mobile phase containing acetylacetone and 1,10-phenanthroline by synergistic extraction effect. After the sample solution is introduced, the mobile phases are delivered into the column by stepwise gradient elution in order of decreasing pH. Each metal ion is concentrated at a pH border formed between the zones of different pH in the column and moves toward the outlet of the column with the pH border. Mutual separation of La(III), Ce(III), Nd(III), Eu(III), Y(III), Tb(III), and Yb(III) was achieved by the present method for an 1-mL sample injection with the column of which the inner volume is 11.8 mL. The multistep pH-peak-focusing liquid chromatography with a hydrophilic polymer gel column developed in this study has great potential as a useful method for the separation of rare earth metal ions on a preparatory scale.

Design optimization for microstrip antennas based on polymethyl methacrylate (PMMA) substrate and carbon nanotube (CNT) conductive material in sub-6 Ghz band

Abstract Background The rapid expansion of modern smart applications, demanding faster data transfer and extensive bandwidth, has prompted the development of new-generation networks like 5G and 6G. These networks encompass additional frequency bands such as sub-6 GHz, millimeter waves, and terahertz bands to meet the growing bandwidth requirements. However, despite the substantial bandwidth available in these bands, several challenges must be addressed to overcome unfavorable propagation characteristics. Moreover, numerous applications necessitate wireless devices with antennas that exhibit high flexibility and exceptional radiation responses, particularly when subjected to bending effects. This requirement highlights the importance of polymers-based antennas that can adapt to changing conditions while maintaining optimal performance. The present comprehensive study delves into the performance evaluation of rectangular and circular microstrip antennas utilizing PMMA (polymethyl methacrylate) polymer substrate with varying thicknesses. Results Notably, CNTs (Carbon Nanotubes) are employed as an alternative to traditional copper for the conductive part and ground plane. Both PMMA-based antennas, integrated with CNTs, exhibit a compact footprint of 27.8 × 47.8 × 1.5 mm3 for the circular antenna and 22.8 × 39.5 × 1.5 mm3 for the rectangular antenna. Impressively, the realized gain of both antennas surpasses 5 dBi, demonstrating robust performance in both flat and bending scenarios across different substrate thicknesses. Conclusions The rectangular antenna achieves a bandwidth of approximately 200 MHz, while the circular microstrip antenna showcase annotable bandwidth of 500 MHz. These exceptional outcomes position the two microstrip antennas as highly suitable for a diverse range of emerging applications within the sub-6 GHz band (the frequency range below 6 GHz in the radio spectrum). Thus, the combination of PMMA substrate, CNTs and the compact form factor of the antennas presents a compelling solution for meeting the demands of modern applications requiring efficient wireless communication with enhanced performance and bandwidth.

Ephedra intermedia Schrenk & C. A. Mey Methanol Extract: Nanoencapsulation by Mini-Emulsion Polymerization and its Release Trend under Simulated Conditions of the Human Body.

In this research, the extract of Ephedra intermedia Schrenk &C.A.Meywas encapsulated using the mini-emulsion polymerization method based on methyl methacrylate polymers with a nanometer size. The encapsulated extract was characterized using different analytical techniques. Furthermore, the loading efficiency and release of the plant extract were examined. FT-IT spectroscopy confirmed the formation of an expectational product. The TEM and SEM imaging showed a spherical morphology for the prepared encapsulated extract. The average size of poly-methyl-methacrylate nanoparticles containing Ephedra extract was found to be approximately 47 nm. The extract loading efficiency and encapsulation efficiency test demonstrated a dose-depending behavior on E. intermedia extract for both analyses, which is highly advantageous for traversing biological barriers. The release assay shows a controlled release for the extract at phosphate buffer solution(PBS). A 38% release was calculated after 36 hours. The results obtained from the present study reveal that encapsulating the plant extract is a suitable alternative to control and increase their medicinal properties.