Integration Of Poly Research Articles

Notably enhanced dielectric response with low loss in PVDF composites filled with RuO2–BaTiO3 hybrid particles

This study delineates the process of fabricating and the results of investigating the dielectric properties of hybrid particles created through the integration of Poly(vinylidene fluoride) (PVDF) filled with RuO2 coated on BaTiO3 nanoparticles (nBT), designated as RuO2–nBT. These hybrid particles were successfully synthesized employing a simple and cost–effective solid–state reaction method. The inclusion of RuO2–nBT in the PVDF matrix engendered a notable enhancement in its dielectric properties. Notably, a RuO2–nBT fraction of 0.5 manifested a dielectric constant (ε′) of 107.4 and a dielectric loss tangent (tanδ) value of 0.062 at 30 °C and 1 kHz. These findings signify the effective role of interfacial polarization occurring between the PVDF matrix and the RuO2–nBT hybrid particles, leading to a marked improvement in dielectric attributes. Moreover, the observed low tanδ value indicates the elimination of conductive pathways, an inhibitory effect attributed to the incorporation of RuO2–nBT hybrid particles. This study underscores the promising potential of RuO2–nBT hybrid particles in fine–tuning and augmenting the dielectric properties of polymer composites, particularly in scenarios necessitating low tanδ and high ε′ values.

Molecular brushes based on poly(amino acid)s: synthesis, structures, and applications

AbstractPolymer science is witnessing rapid advancements in the precision construction of synthetic macromolecules. Beyond the impressive advances in molecular brush, the integration of poly(amino acid)s into bottlebrush architectures leads to a novel class of materials known as molecular brushes based on poly(amino acid)s (MBPAs). These materials not only possess biorelated functions but also enable the incorporation of the diverse secondary structures found in poly(amino acid)s into the bulk polymers. Here we present a comprehensive and critical summary of three synthetic strategies and three different constructions for MBPAs. Furthermore, we highlight their potential in the development of advanced materials for a broad range of applications, encompassing antimicrobial activity, pharmaceutical delivery, and bioimaging.

Facile Synthesis and Integration of Poly(vinyl alcohol) Sponge-Supported Metal Nanocatalysts on a Microfluidic Chip Enable a New Continuous Flow Multireactor Nanocatalysis Platform for High Efficiency and Reusability Catalysis

Facile Synthesis and Integration of Poly(vinyl alcohol) Sponge-Supported Metal Nanocatalysts on a Microfluidic Chip Enable a New Continuous Flow Multireactor Nanocatalysis Platform for High Efficiency and Reusability Catalysis

Thermoresponsive, Pyrrolidone‐Based Antifouling Polymer Brushes

AbstractCommonly, modification of surfaces with thermoresponsive polymers is performed using poly(N‐isopropylacrylamide) (poly(NIPAM)). However, integration of poly(NIPAM) with a second polymer to obtain more complex copolymer structures has proven challenging due to inherently poorly controllable polymerization characteristics of acrylamides. In this study, (N‐(2‐methacryloyloxyethyl)pyrrolidone (NMEP) is synthesized and polymerized under controlled conditions from silicon oxide substrates via surface‐initiated atom transfer radical polymerization (SI‐ATRP) to produce thermoresponsive poly(NMEP) brushes. The livingness of the brushes is demonstrated by reinitiation of poly(NMEP) brushes using oligo(ethylene glycol) methyl ether methacrylate to obtain diblock copolymer brushes. Following extensive characterization, the reversible thermoresponsive behavior of these poly(NMEP) brushes is demonstrated using phase‐controlled AFM topography measurements in an aqueous liquid environment. These measurements indicate that at 27 °C the poly(NMEP) brushes are solvated and extend away from the surface, whereas at 60 °C the polymers are insoluble and reside in a collapsed conformation. Finally, to investigate the potential applicability of poly(NMEP) brushes in biomedical devices, the antifouling properties of the coating are tested in aqueous media containing BSA, fibrinogen, or 10% diluted human serum using quartz crystal microbalance with dissipation monitoring (QCM‐D). These measurements reveal very good antifouling properties, even when exposed to 10% diluted human serum.

Effect of melt spinning on the integrity of poly(ether ether ketone) for commingled yarn based composite preforms

PEEK yarns are used for commingled yarn based preforms in order to manufacture high performance thermoplastic composites. In a previous work, characterizations of PEEK commingled yarns revealed degradation, causing poor consolidation of final composites. The sizing applied onto the yarn surface in the melt spinning was identified as a degradation factor. Thus, the aim of this work is to assess the effect of different melt spinning parameters: extrusion, sizing and draw ratio, on PEEK integrity and its degradation process. Yarns at different stages of melt spinning were characterized through various techniques. For all yarns, degradation was identified during further transformation, in the molten state, inducing a decrease of the crystallization temperature and an increase of viscosity due to crosslinking. Extrusion initiates degradation earlier without changing the PEEK decomposition process. Sizing is responsible for an acceleration and modifications of degradation steps.

Corrigendum: “In vivo integration of poly(ε‐ caprolactone)/gelatin nanofibrous nerve guide seeded with teeth derived stem cells for peripheral nerve regeneration”

Corrigendum: “<i>In vivo</i> integration of poly(ε‐ caprolactone)/gelatin nanofibrous nerve guide seeded with teeth derived stem cells for peripheral nerve regeneration”

Semi-convertible Hydrogel Enabled Photoresponsive Lubrication

Summary A semi-convertible hydrogel with reversible photoresponsive supramolecular lubricating ability is demonstrated by integrating a responsive supramolecular system of α-cyclodextrins/polyethylene glycol (α-CD/PEG) and competitive guest 1-[p-(phenylazo)benzyl]pyridinium bromide (AzoPB) within a poly(vinyl alcohol) (PVA) and polyacrylamide (PAAm) framework. The competitive host-guest interaction between α-CD/PEG supramolecular network and AzoPB after UV and visible-light irradiation enables the appearance and disappearance of the sol-state layer on the hydrogel surface while the PVA and PAAm consistently keeps the framework. This semi-convertible process realizes the reversible photoresponsive lubricating ability and variable toughness. We envision that this finding will offer a possible way for fabricating novel smart devices far beyond lubrication, leading to an emerging branch of interdisciplinary materials science that integrates supramolecular chemistry, hydrogel, and surface science.

Magnetic reduced graphene oxide loaded hydrogels: Highly versatile and efficient adsorbents for dyes and selective Cr(VI) ions removal

The formation of composites of reduced graphene oxide (rGO) and magnetic nanoparticles (MP) has flourished in recent years as they combine the advantages of both nanomaterials. Most of these composite materials are prepared by in situ formation of MP onto rGO or by the post-adsorption onto rGO. We report here on a simple and highly controlled method for the fabrication of different magnetic 3D rGO-loaded hydrogels. Cellulose bound magnetic nanoparticles (MP@cellulose) were synthesized by chemical co-precipitation and loaded together with rGO into poly(ethylene glycol) dimethacrylate based hydrogels during their fabrication using photo-polymerization. The magnetic rGO-loaded hydrogels proved to be highly adaptable to different applications. The as-formed composites allowed for efficient dye removal with an adsorption capacity of 111.9±4mgg−1 in the case of methylene blue (MB). Integration of poly(ethyleneimine) (PEI) allowed for the selective capturing of Cr6+ ions with an adsorption capacity of 313±12mgg−1. Most importantly, independent of the application, the magnetic rGO-loaded hydrogel can be regenerated without loss of its adsorption capacity.

Synthesis and integration of poly(1-vinylimidazole) polymer electrolyte in dye sensitized solar cells by initiated chemical vapor deposition

Initiated chemical vapor deposition (iCVD) is used to integrate poly(1-vinylimidazole) (PVIZ) into the mesoporous photoanode of dye sensitized solar cells (DSSCs). To our knowledge, this is the first reported demonstration of PVIZ via iCVD as a novel polymer electrolyte in DSSCs. Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS) verified the iCVD polymer as stoichiometric PVIZ. Polymer deposition rate was found to increase with increasing reactor pressure and decreasing substrate temperature. The kinetic studies further determined that the surface polymerization reaction is first order with respect to the surface monomer concentration. The power conversion efficiency of DSSCs incorporating crosslinked PVIZ was found to be 27% higher than that of liquid electrolyte DSSCs as a result of higher open circuit voltage and short circuit current.

Integration of poly(3-hexylthiophene) conductive stripe patterns with 3D tubular structures for tissue engineering applications

P3HT was self-assembled into large-scale conductive stripe patterns based on confined evaporative self-assembly. These conductive stripe patterns could induce cell alignment and provide spatial electric signals to modulate cellular behaviors.

In vivointegration of poly(ε-caprolactone)/gelatin nanofibrous nerve guide seeded with teeth derived stem cells for peripheral nerve regeneration

Artificial nanofiber nerve guides have gained huge interest in bridging nerve gaps and associated peripheral nerve regeneration due to its high surface area, flexibility and porous structure. In this study, electrospun poly (ε-caprolactone)/gelatin (PCL/Gel) nanofibrous mats were fabricated, rolled around a copper wire and fixed by medical grade adhesive to obtain a tubular shaped bio-graft, to bridge 10 mm sciatic nerve gap in in vivo rat models. Stem cells from human exfoliated deciduous tooth (SHED) were transplanted to the site of nerve injury through the nanofibrous nerve guides. In vivo experiments were performed in animal models after creating a sciatic nerve gap, such that the nerve gap was grafted using (i) nanofiber nerve guide (ii) nanofiber nerve guide seeded with SHED (iii) suturing, while an untreated nerve gap remained as the negative control. In vitro cell culture study was carried out for primary investigation of SHED-nanofiber interaction and its viability within the nerve guides after 2 and 16 weeks of implantation time. Walking track analysis, plantar test, electrophysiology and immunohistochemistry were performed to evaluate functional recovery during nerve regeneration. Vascularization was also investigated by hematoxilin/eosine (H&E) staining. Overall results showed that the SHED seeded on nanofibrous nerve guide could survive and promote axonal regeneration in rat sciatic nerves, whereby the biocompatible PCL/Gel nerve guide with cells can support axonal regeneration and could be a promising tissue engineered graft for peripheral nerve regeneration.

Morphological Phase Behavior of Poly(RTIL)-Containing Diblock Copolymer Melts

The development of nanostructured polymeric systems containing directionally continuous poly(ionic liquid) (poly(IL)) domains has considerable implications toward a range of transport-dependent, energy-based technology applications. The controlled, synthetic integration of poly(IL)s into block copolymer (BCP) architectures provides a promising means to this end, based on their inherent ability to self-assemble into a range of defined, periodic morphologies. In this work, we report the melt-state phase behavior of an imidazolium-containing alkyl–ionic BCP system, derived from the sequential ring-opening metathesis polymerization (ROMP) of imidazolium- and alkyl-substituted norbornene monomer derivatives. A series of 16 BCP samples were synthesized, varying both the relative volume fraction of the poly(norbornene dodecyl ester) block (fDOD = 0.42–0.96) and the overall molecular weights of the block copolymers (Mn values from 5000–20 100 g mol–1). Through a combination of small-angle X-ray scattering (SAXS) and dynamic rheology, we were able to delineate clear compositional phase boundaries for each of the classic BCP phases, including lamellae (Lam), hexagonally packed cylinders (Hex), and spheres on a body-centered-cubic lattice (SBCC). Additionally, a liquid-like packing (LLP) of spheres was found for samples located in the extreme asymmetric region of the phase diagram, and a persistent coexistence of Lam and Hex domains was found in lieu of the bicontinuous cubic gyroid phase for samples located at the intersection of Hex and Lam regions. Thermal disordering was opposed even in very low molecular weight samples, detected only when the composition was highly asymmetric (fDOD = 0.96). Annealing experiments on samples exhibiting Lam and Hex coexistence revealed the presence of extremely slow transition kinetics, ultimately selective for one or the other but not the more complex gyroid phase. In fact, no evidence of the bicontinuous network was detected over a 2 month annealing period. The ramifications of these results for transport-dependent applications targeting the use of highly segregated poly(IL)-containing BCP systems are carefully considered.

Application of acid-catalyzed hydrolysis of dispersed organic solvent in developing new microencapsulation process technology

The aim of this study was to evaluate a new microencapsulation technology employing an acid-catalyzed solvent extraction method in conjunction to an emulsion-based microencapsulation process. Its process consisted of emulsifying a dispersed phase of poly(D,L-lactide-co-glycolide) and isopropyl formate in an aqueous phase. This step was followed by adding hydrochloric acid to the resulting oil-in-water emulsion, in order to initiate the hydrolysis of isopropyl formate dissolved in the aqueous phase. Its hydrolysis caused the liberation of water-soluble species, that is, isopropanol and formic acid. This event triggered continual solvent leaching out of emulsion droplets, thereby initiating microsphere solidification. This new processing worked well for encapsulation of progesterone and ketoprofen that were chosen as a nonionizable model drug and a weakly acidic one, respectively. Furthermore, the structural integrity of poly(D,L-lactide-co-glycolide) was retained during microencapsulation. The new microencapsulation technology, being conceptually different from previous approaches, might be useful in preparing various polymeric particles.

Conducting Block Copolymer Nanowires Containing Regioregular Poly(3‐Hexylthiophene) and Polystyrene

Grignard Metathesis polymerization (GRIM) for the synthesis of regioregular poly(3‐alkylthiophenes) proceeds via a “living” chain growth mechanism. Due to the “living” nature of this polymerization regioregular poly(3‐alkylthiophenes) with predetermined molecular weight, narrow molecular weight distributions and desired chain end functionality are now readily available. Allyl terminated poly(3‐hexylthiophene) was successfully used as a precursor for the synthesis of di‐block copolymers containing polystyrene. The addition of “living” poly(styryl)lithium to the allyl terminated regioregular poly(3‐hexylthiophene) generated the di‐block copolymer. Poly(3‐hexylthiophene)‐b‐polystyrene was also synthesized by atom transfer radical polymerization. Integration of poly(3‐hexylthiophene) in di‐block copolymers with polystyrene leads to the formation of nanowire morphology and self‐ordered conducting nanostructured materials.

Effects of Thermal and Mechanical Loading on PDC Bit Life

Summary Results of numerical analyses to determine the effects of thermal and mechanical loading on the integrity of poly crystalline-diamond-compact (PDC) cutters during deep-hole drilling are presented. Cutter-temperature distributions for several drilling environments are combined with the appropriate mechanical cutting loads to predict stress distributions for the study of cutter wear mechanisms. A discussion of wear mechanisms acting on the cutting structure is presented. Suggestions based on these analyses are presented for the operation of PDC bits to increase bit life in hard, abrasive rock drilling. Microstructural design considerations for the cemented carbide that supports the diamond layer are also discussed.