scholarly journals Preparation of self-healing hydrogel toward improving electromagnetic interference shielding and energy efficiency

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Reza Peymanfar ◽  
Elnaz Selseleh-Zakerin ◽  
Ali Ahmadi ◽  
Ardeshir Saeidi ◽  
Seyed Hassan Tavassoli

AbstractIn this study, a self-healing hydrogel was prepared that is transparent to visible (Vis) light while absorbing ultraviolet (UV), infrared (IR), and microwave. The optothermal features of the hydrogel were explored by monitoring temperature using an IR thermometer under an IR source. The hydrogel was synthesized using sodium tetraborate decahydrate (borax) and polyvinyl alcohol (PVA) as raw materials based on a facile thermal route. More significantly, graphene oxide (GO) and graphite-like carbon nitride (g-C3N4) nanostructures as well as carbon microsphere (CMS) were applied as guests to more dissect their influence on the microwave and optical characteristics. The morphology of the fillers was evaluated using field emission scanning electron microscopy (FE-SEM). Fourier transform infrared (FTIR) attested that the chemical functional groups of the hydrogel have been formed and the result of diffuse reflection spectroscopy (DRS) confirmed that the hydrogel absorbs UV while is transparent in Vis light. The achieved result implied that the hydrogel acts as an essential IR absorber due to its functional groups desirable for energy efficiency and harvesting. Interestingly, the achieved results have testified that the self-healing hydrogels had the proper self-healing efficiency and self-healing time. Eventually, microwave absorbing properties and shielding efficiency of the hydrogel, hydrogel/GO, g-C3N4, or CMS were investigated, demonstrating the salient microwave characteristics, originated from the established ionic conductive networks and dipole polarizations. The efficient bandwidth of the hydrogel was as wide as 3.5 GHz with a thickness of 0.65 mm meanwhile its maximum reflection loss was 75.10 dB at 14.50 GHz with 4.55 mm in thickness. Particularly, the hydrogel illustrated total shielding efficiency (SET) > 10 dB from 1.19 to 18 and > 20 dB from 4.37 to 18 GHz with 10.00 mm in thickness. The results open new windows toward improving the shielding and energy efficiency using practical ways.

Polymers ◽  
2018 ◽  
Vol 11 (1) ◽  
pp. 41 ◽  
Author(s):  
Ali Berkem ◽  
Ahmet Capoglu ◽  
Turgut Nugay ◽  
Erol Sancaktar ◽  
Ilke Anac

The self-healing ability can be imparted to the polymers by different mechanisms. In this study, self-healing polydimethylsiloxane-graft-polyurethane (PDMS-g-PUR)/Vanadium pentoxide (V2O5) nanofiber supramolecular polymer composites based on a reversible hydrogen bonding mechanism are prepared. V2O5 nanofibers are synthesized via colloidal route and characterized by XRD, SEM, EDX, and TEM techniques. In order to prepare PDMS-g-PUR, linear aliphatic PUR having one –COOH functional group (PUR-COOH) is synthesized and grafted onto aminopropyl functionalized PDMS by EDC/HCl coupling reaction. PUR-COOH and PDMS-g-PUR are characterized by 1H NMR, FTIR. PDMS-g-PUR/V2O5 nanofiber composites are prepared and characterized by DSC/TGA, FTIR, and tensile tests. The self-healing ability of PDMS-graft-PUR and composites are determined by mechanical tests and optical microscope. Tensile strength data obtained from mechanical tests show that healing efficiencies of PDMS-g-PUR increase with healing time and reach 85.4 ± 1.2 % after waiting 120 min at 50 °C. The addition of V2O5 nanofibers enhances the mechanical properties and healing efficiency of the PDMS-g-PUR. An increase of healing efficiency and max tensile strength from 85.4 ± 1.2% to 95.3 ± 0.4% and 113.08 ± 5.24 kPa to 1443.40 ± 8.96 kPa is observed after the addition of 10 wt % V2O5 nanofiber into the polymer.


Crystals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 752
Author(s):  
Mian Luo ◽  
Kang Jing ◽  
Jingquan Bai ◽  
Ziqi Ding ◽  
Dingyi Yang ◽  
...  

The autogenous healing potential of cement-based materials is affected by multiple factors, such as mix composition, crack width, pre-cracking age and external environmental conditions. In this study, the effects of curing conditions and supplementary cementitious materials (SCMs) on autogenous self-healing of early age cracks in cement mortar were investigated. Three curing conditions, i.e., standard curing, wet–dry cycles and incubated in water, and two SCMs, i.e., fly ash (FA) and blast furnace slag (BFS) with various contents (cement replacement ratio at 0%, 20%, and 40%) were examined. A single early age crack (pre-cracking age of 3 days) with a width of 200~300 μm was generated in cylindrical mortar specimens. Autogenous crack self-healing efficiency of mortar specimens was evaluated by performing a visual observation and a water permeability test. Moreover, microstructure analysis (XRD, SEM and TG/DTG) was utilized to characterize the healing products. The results indicated that the presence of water was essential for the autogenous self-healing of early age cracks in cement mortar. The efficiency of self-healing cracks was highest in specimens incubated in water. However, no significant self-healing occurred in specimens exposed to standard curing. For wet–dry cycles, a longer healing time was needed to obtain good self-healing compared to samples incubated in water. SCMs type and content significantly affected the autogenous self-healing ability of early age cracks. The self-healing efficiency of early age cracks decreased with increases in FA and BFS content. BFS mortars exhibited greater recovery in relation to water penetration resistance compared to the reference and FA mortars. Almost the same regain of water tightness and a lower crack-healing ratio after healing of 28 days in FA mortars were observed compared to the reference. The major healing product in the surface cracks of specimens with and without SCMs was micron-sized calcite crystals with a typical rhombohedral morphology.


Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2753
Author(s):  
Maria Kosarli ◽  
Anastasia Polymerou ◽  
Georgios Foteinidis ◽  
Christos Vazouras ◽  
Alkiviadis S. Paipetis

In this study, the effect of the addition of multi-walled carbon nanotubes (MWCNTs), at three percentages, into the urea-formaldehyde (UF) shell-wall of microcapsules on the healing efficiency is reported. The modified shell-wall created a conductive network in semi-conductive epoxies, which led to an improvement of the electromagnetic interference shielding effectiveness (EMI SE); utilizing the excellent electrical properties of the CNTs. The microcapsule’s mean diameter and shell wall were examined via scanning electron microscopy (SEM). Thermal stability was evaluated via thermogravimetric analysis (TGA). The healing efficiency was assessed in terms of fracture toughness, while the electrical properties were measured using impedance spectroscopy. The measurements of the EMI SE were carried out in the frequency range of 7–9 GHz. The derived results indicated that the incorporation of the CNTs resulted in a decrease in the mean size of the microcapsules, while the thermal stability remained unchanged. In particular, the introduction of 0.5% w/v CNTs did not affect the healing efficiency, while it increased the initial mechanical properties of the epoxy after the incorporation of the self-healing system by 27%. At the same time, it led to the formation of a conductive network, providing electrical conductivity to the epoxies. The experimental results showed that the SE increased on average 5 dB or more after introducing conductive microcapsules.


Materials ◽  
2021 ◽  
Vol 14 (21) ◽  
pp. 6431
Author(s):  
Peng Yang ◽  
Li-Qing Wang ◽  
Xu Gao ◽  
Sai Wang ◽  
Jun-Feng Su

It has become one of the research directions of intelligent materials for self-healing asphalt pavements to use a bionic microvascular containing oily rejuvenator. The rejuvenator in a microvascular can carry out the healing of asphalt micro-cracks, thus reducing the damage to and prolonging the life of asphalt pavement. The aim of this work was to investigate the smart self-healing capability of an asphalt/microvascular material through its microstructure and mechanical properties. Microstructure observation indicated no interface separation between the microvasculars and bitumen matrix. Micro-CT images showed that microvasculars dispersed in asphalt samples without accumulation or tangles. The phenomenon of microcracks healing without intervention was observed, which proved that the fractured asphalt sample carried out the self-healing process with the help of rejuvenator diffusing out from the broken microvasculars. The self-healing efficiency of asphalt samples was also evaluated through a tensile test considering the factors of microvasculars content, healing time and healing temperature. It was found that the tensile strength of the asphalt samples was greatly enhanced by the addition of microvasculars under a set test condition. Self-healing efficiency was enhanced with more broken microvasculars in the rupture interface of the asphalt sample. During two self-healing cycles, the self-healing efficiency of the asphalt sample with three microvascular per 1 cm2 of a broken interface were able to reach 80% and 86%. This proves that microvasculars containing rejuvenator play a practical role in the self-healing process of asphalt. With an increase in temperature from 0 to 30 °C, the self-healing capability of the asphalt samples increased dramatically. An increase in time increased the self-healing capability of the bitumen samples. At last, a preliminary mathematical model also deduced that the self-healing efficiency was determined by the individual healing steps, including release, penetration and diffusion of the rejuvenator agent.


2007 ◽  
Vol 4 (13) ◽  
pp. 389-393 ◽  
Author(s):  
Timothy C Mauldin ◽  
Joseph D Rule ◽  
Nancy R Sottos ◽  
Scott R White ◽  
Jeffrey S Moore

While original epoxy resin-based self-healing systems used the commercially available endo -isomer of dicyclopentadiene (DCPD), the exo -stereoisomer is known to have much faster olefin metathesis reaction rates with first-generation Grubbs' catalyst. Here, we measure the energy to failure of healed specimens as a function of healing time and compare the kinetics of damage repair for endo - and exo -DCPD, and mixtures of the two isomers. Using catalyst loading levels previously reported to be effective for endo -DCPD, exo -DCPD was found to heal approximately 20 times faster than the endo- isomer, but with a lower healing efficiency. The fracture toughness of the repaired specimens decreased when the exo content of the blends was greater than 40% and, for the pure exo -DCPD, when the catalyst loadings were below 1%. Possible causes of the reduced healing efficiencies of the exo -DCPD healing agent are discussed.


2020 ◽  
Author(s):  
Alexis Wolfel ◽  
Cecilia Inés Alvarez Igarzabal ◽  
Marcelo Ricardo Romero

<p>Design of materials with novel sensitivities and smart behaviour is important for the development of smart systems with automated responsiveness. We have recently reported the synthesis of hydrogels, cross-linked by <i>N,N'</i>-diallyltartardiamide (DAT). The covalent DAT-crosslinking points have vicinal diols which can be easily cleaved with periodate, generating valuable a-oxo-aldehyde functional groups, useful for further chemical modification. Based on those findings, we envisioned that a self-healable hydrogel could be obtained by incorporation of primary amino functional groups, from <a>2-aminoethyl methacrylate </a>hydrochloride (AEMA), coexisting with DAT into the same network. The a-oxo-aldehyde groups generated after the reaction with periodate would arise in the immediate environment of amine groups to form imine cross-links. For this purpose, DAT-crosslinked hydrogels were synthesized and carefully characterized. The cleavage of DAT-crosslinks with periodate promoted changes in the mechanical and swelling properties of the materials. As expected, a self-healing behavior was observed, based on the spontaneous formation of imine covalent bonds. In addition, we surprisingly found a combination of fast vicinal diols cleavage and a low speed self-crosslinking reaction by imine formation. Consequently, it was found a time-window in which a periodate-treated polymer was obtained in a transient liquid state, which can be exploited to choose the final shape of the material, before automated gelling. The singular properties attained on these hydrogels could be useful for developing sensors, actuators, among other smart systems.</p>


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yuyan Wang ◽  
Xin Huang ◽  
Xinxing Zhang

AbstractSelf-healing materials integrated with excellent mechanical strength and simultaneously high healing efficiency would be of great use in many fields, however their fabrication has been proven extremely challenging. Here, inspired by biological cartilage, we present an ultrarobust self-healing material by incorporating high density noncovalent bonds at the interfaces between the dentritic tannic acid-modified tungsten disulfide nanosheets and polyurethane matrix to collectively produce a strong interfacial interaction. The resultant nanocomposite material with interwoven network shows excellent tensile strength (52.3 MPa), high toughness (282.7 MJ m‒3, which is 1.6 times higher than spider silk and 9.4 times higher than metallic aluminum), high stretchability (1020.8%) and excellent healing efficiency (80–100%), which overturns the previous understanding of traditional noncovalent bonding self-healing materials where high mechanical robustness and healing ability are mutually exclusive. Moreover, the interfacical supramolecular crosslinking structure enables the functional-healing ability of the resultant flexible smart actuation devices. This work opens an avenue toward the development of ultrarobust self-healing materials for various flexible functional devices.


Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 201
Author(s):  
Stefano Paolillo ◽  
Ranjita K. Bose ◽  
Marianella Hernández Santana ◽  
Antonio M. Grande

This article reviews some of the intrinsic self-healing epoxy materials that have been investigated throughout the course of the last twenty years. Emphasis is placed on those formulations suitable for the design of high-performance composites to be employed in the aerospace field. A brief introduction is given on the advantages of intrinsic self-healing polymers over extrinsic counterparts and of epoxies over other thermosetting systems. After a general description of the testing procedures adopted for the evaluation of the healing efficiency and the required features for a smooth implementation of such materials in the industry, different self-healing mechanisms, arising from either physical or chemical interactions, are detailed. The presented formulations are critically reviewed, comparing major strengths and weaknesses of their healing mechanisms, underlining the inherent structural polymer properties that may affect the healing phenomena. As many self-healing chemistries already provide the fundamental aspects for recyclability and reprocessability of thermosets, which have been historically thought as a critical issue, perspective trends of a circular economy for self-healing polymers are discussed along with their possible advances and challenges. This may open up the opportunity for a totally reconfigured landscape in composite manufacturing, with the net benefits of overall cost reduction and less waste. Some general drawbacks are also laid out along with some potential countermeasures to overcome or limit their impact. Finally, present and future applications in the aviation and space fields are portrayed.


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