RESUMEN
The exploration of 'electrostatic self-assembly' on solid surfaces has garnered significant interest across various fields. With the sophistication of gadgets, managing electromagnetic interference (EMI) from stray signals, especially in stealth applications, necessitates materials that can absorb microwaves. A promising approach involves integrating lightweight self-healing polymeric materials. This study employs electrostatic self-assembly to design a carbon nanotube structure on an interpenetrating polymer network (IPN) made of PVDF and bismaleimide (BMI)-grafted dopamine hydrochloride, enhancing mechanical integrity through well-formed IPNs. Graphene oxide (GO) is introduced before IPN formation to facilitate an 'acceptor-donor' interaction via the Diels-Alder adduct between BMI and GO, which binds with multi-walled carbon nanotubes (MWCNTs). MWCNTs, modified with PQ7 or PDDA for a positive charge, self-assemble onto the IPN-GO construct, creating a lightweight and chemically stable structure capable of absorbing electromagnetic radiation. The 21 µm thick construct exhibits enhanced microwave absorption within the X-band (8.2-12.4 GHz), with a specific shielding effectiveness of 8637 dB cm2 g-1 and a green index (gs ≈ 1.41). The construct is coated with self-healable polyetherimide (PEI) containing exchangeable disulfide bonds to address maintenance challenges, providing heat-triggered self-healing properties. These innovative structures offer solutions for 5G and IoT applications where lightweight, durable, and multifunctional properties are essential for effectively shielding electronic devices from stray signals.
RESUMEN
Carbon fiber-reinforced epoxy (CFRE) laminates have attracted significant attention as a structural material specifically in the aerospace industry. In recent times, various strategies have been developed to modify the carbon fiber (CF) surface as the interface between the epoxy matrix and CFs plays a pivotal role in determining the overall performance of CFRE laminates. In the present work, graphene oxide (GO) was used to tag a polyetherimide (PEI, termed BA) containing exchangeable bonds and was employed as a sizing agent to improve the interfacial adhesion between CFs and epoxy. This unique GO-tagged-BA sizing agent termed BAGO significantly enhanced the mechanical properties of CFRE laminates by promoting stronger interactions between CFs and the epoxy matrix. The successful synthesis of BAGO was verified by Fourier-transform infrared spectroscopy. Additionally, the partial reduction of GO owing to this tagging with BA was further confirmed by X-ray diffraction and Raman spectroscopy, and the thermal stability of this unique sizing agent was evaluated using thermogravimetric analysis. The amount of GO in BAGO was optimized as 0.25 wt% of BA termed 0.25-BAGO. The 0.25-BAGO sizing agent resulted in a significant increase in surface roughness, from 15 nm to 140 nm, and surface energy, from 13.2 to 34.7 mN m-1 of CF. The laminates prepared from 0.25-BAGO exhibited a remarkable 40% increase in flexural strength (FS) and a 35% increase in interlaminar shear strength (ILSS) due to interfacial strengthening between epoxy and CFs. In addition, these laminates exhibited a self-healing efficiency of 51% in ILSS due to the presence of dynamic disulfide bonds in BAGO. Interestingly, the laminates with 0.25-BAGO exhibited enhanced Joule heating and enhanced deicing, though the EMI shielding efficiency slightly declined.
RESUMEN
According to current projections, of the 400 mega tons of plastic produced globally, 70% is waste and of that only 16% is recycled and the rest is incinerated. This is estimated to contribute to ca. 16% of the net carbon emission by 2050. Such a massive amount of unmanaged plastic waste and the associated huge carbon footprint sets a significant challenge to tackle in the coming decades. To achieve net-zero carbon emission, closed-loop circular economy in plastics is crucial but collection, sorting and processing the postconsumer recycled (PCR) plastics poses humongous challenge in achieving this circularity, unless an effective strategy is designed. In a first of its kind, a designer biobased molecule was synthesized (here maleated castor oil, mCO) that is steric and thermally stable and forms in situ "homo-cross-linking" in the melt post grafting onto PCR-PP. This designer molecule, besides offering a transient network, helps bridge the fragmented PP chains which is usually not amenable from the traditional grafting (like maleic anhydride), thereby addressing a long-standing challenge of retaining the properties post grafting due to chain scission in the melt. The resulting maleated (m) PCR-PP now offers abundant functionality which helped us design single and dual covalent adaptable network (CANs) and evaluate their consequences on the structure-property correlation. The PCR-PP Vitrimers demonstrate a distinct rubbery plateau in the melt and reprocessability with >90% recovery in mechanical properties even after the fifth sequence of recycling. We propose here for the first time how the varying reactivity (single or dual) in the transient polymer network, through dynamic exchange, regulates the closed-loop circularity in PP Vitrimers. Our results begin to suggest that the varying reactivity should be taken into account as an additional design parameter, as it influences both the stress relaxation rates and the flow activation energy. We now understand that the topology reconfiguration is strongly dependent on this varying reactivity, which also controls the overall crystalline morphology and the structural properties in the Vitrimers. This study, in addition to opening new avenues for recycling PP, will help guide researchers working in this field from both academia and industry.
RESUMEN
In the era of fifth-generation networks and the Internet of Things, new classes of lightweight, ultrathin, and multifunctional electromagnetic interference (EMI) shielding materials have become inevitable prerequisites for the protection of electronics from stray electromagnetic signals. In the present study, for the first time, we have designed a unique nanohybrid composed of a copper-based polyoxometalate (Cu-POM)-immobilized carbon nanotube construct, having a micron (â¼100 µm)-level thickness, through a facile vacuum-assisted filtration technique. In this course of study, a total of four Cu-POMs, two from each category of Keggin and Anderson bearing opposite charges, i.e., positive and negative, have been rationally selected to investigate the effects of the host-guest electrostatic interaction between CNT and POMs in the EMI shielding performance. This approach of the host-guest electrostatic assembly between Cu-based polyanionic oxo clusters and counter-charged CNTs in the construct synergistically enhances the EMI shielding performance compared to the individual components dominated by 90% absorption in the X-band (8.2-12.4 GHz) frequency regime. Further, mutable EMI SE can be achieved by tuning the concentration of POMs and CNTs with different weight ratios. Such Cu-POM-immobilized CNT constructs demonstrating excellent shielding (â¼45 dB) are not amenable via any other conventional routes, including flakes and dispersion.
RESUMEN
The widespread use of miniaturized electronic gadgets today faces stiff reliability obstacles from factors like stray electromagnetic signals. The challenge is to design lightweight shielding materials that combine small volume and high-frequency operations to reliably reduce/eliminate electromagnetic interference. Herein, in the first of its kind, a sequential interpenetrating polymeric network (IPN) membrane was used to host a CNT construct through a stimuli-responsive trigger. The proposed construct besides being robust, sustainable, and scalable is a universal approach to fabricate a CNT construct where conventional strategies are not amenable. This approach of self-assembling counter-charged CNTs also maximizes the number of CNTs in the final construct, thereby greatly enhancing the shielding performance dominated by 90% absorption in a wide frequency band of 8.2-26.5 GHz. The IPN-CNT construct achieves specific shielding effectiveness in the range of ca. 1607-5715 dB cm2 g-1 by tuning the thickness of the CNT construct with an endearing green index (gs ≈ 1.8). The performance of such an ultra-thin, light-weight IPN-CNT construct remained unchanged when subjected to 10 000 bending cycles and on exposure to different chemical environments, indicating outstanding mechanical/chemical stability.
RESUMEN
Fe3O4@SiO2@PPy core-shell nanocomposites were fabricated by the coating of SiO2 on Fe3O4 through base catalyzed hydrolysis of tetraethyl orthosilicate followed by encapsulation of polypyrrole (PPy). Subsequently, these trilaminar composites have been characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, Brunauer-Emmett-Teller, superconducting quantum interference devices, and measurement of the total shielding efficiency in the frequency range of 2-8 GHz. Our findings showed the highest total shielding efficiency (â¼32 dB) of Fe3O4@SiO2@PPy (Fe3O4@SiO2/pyrrole wt/wt = 1:9) and followed reflection as the dominant shielding mechanism. Such performance was attributed to poor impedance matching between the PPy (conducting)/SiO2 (insulating) and high electrical conductivity of Fe3O4@SiO2@PPy. Alternatively, electromagnetic (EM) waves incident on the SiO2@PPy interface could also account for enhancing the total shielding efficiency of Fe3O4@SiO2@PPy because of multireflection/refraction. Our earlier work also showed excellent total shielding efficiency of Fe3O4@C@PANI nanocomposites, through absorption as the dominant shielding mechanism. These findings clearly suggest that EM interference shielding in Fe3O4@SiO2@PPy and Fe3O4@C@PANI trilaminar core@shell nanocomposites is controlled by tuning of the shells through switching of the mechanism.
RESUMEN
Polyaniline hollow microsphere (PNHM)/Fe3O4 magnetic nanocomposites have been synthesized by a novel strategy and characterized. Subsequently, PNHM/Fe3O4-40 (Fe3O4 content: 40 wt.%) was used as an adsorbent for the removal of arsenic (As) from the contaminated water. Our investigations showed 98-99% removal of As(III) and As(V) in the presence of PNHM/Fe3O4-40 following pseudo-second-order kinetics (R2 > 0.97) and equilibrium isotherm data fitting well with Freundlich isotherm (R2 > 0.98). The maximum adsorption capacity of As(III) and As(V) correspond to 28.27 and 83.08 mg g-1, respectively. A probable adsorption mechanism based on X-ray photoelectron spectroscopy analysis was also proposed involving monodentate-mononuclear/bidentate-binuclear As-Fe complex formation via legend exchange. In contrast to NO3- and SO42- ions, the presence of PO43- and CO32- co-ions in contaminated water showed decrease in the adsorption capacity of As(III) due to the competitive adsorption. The regeneration and reusability studies of spent PNHM/Fe3O4-40 adsorbent showed ~83% of As(III) removal in the third adsorption cycle. PNHM/Fe3O4-40 was also found to be very effective in the removal of arsenic (<10 µg L-1) from naturally arsenic-contaminated groundwater sample.