Redox- and pH-responsive polymer gels with reversible sol–gel transitions and self-healing properties

RSC Advances ◽  
2014 ◽  
Vol 4 (88) ◽  
pp. 47361-47367 ◽  
Author(s):  
Ping Zhang ◽  
Fengyang Deng ◽  
Ya Peng ◽  
Hongbiao Chen ◽  
Yong Gao ◽  
...  

Redox- and pH-responsive polymer gel with self-healing property was prepared by crosslinking of benzhydrazide-containing polytriazole with a disulfide-containing dialdehyde.

2017 ◽  
Vol 8 (7) ◽  
pp. 1263-1271 ◽  
Author(s):  
Ruixue Chang ◽  
Heng An ◽  
Xu Li ◽  
Ruyi Zhou ◽  
Jianglei Qin ◽  
...  

P(NIPAM-co-FPA) contains an aldehyde group and a phenolic ester moiety is synthesized. The aldehyde group can form reversible covalent bonds with hydrazide to endow the polymer gels with self-healing properties. The self-healable polymer gel can be degraded in Na2CO3 solution based on cleavage of phenolic ester bond.


Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 490 ◽  
Author(s):  
Haifeng Zhao ◽  
Heng An ◽  
Baozhong Xi ◽  
Yan Yang ◽  
Jianglei Qin ◽  
...  

Self-healing hydrogels have drawngreat attention in the past decade since the self-healing property is one of the characteristics of living creatures. In this study, poly(acrylamide-stat-diacetone acrylamide) P(AM-stat-DAA) with a pendant ketone group was synthesized from easy accessible monomers, and thermo-responsive self-healing hydrogels were prepared through a series of diacylhydrazide compounds cross-linking without any additional stimulus. Although the copolymers do not show thermo-response, the hydrogels became thermo-responsive andboth the lower critical solution temperature (LCST) and upper critical solution temperature (UCST) varied with the composition of the copolymer and structure of cross-linkers. With a dynamic covalent bond connection, the hydrogel showed gel-sol-gel transition triggered by acidity, redox, and ketone to acylhydrazide group ratios. This is another interesting cross-linking induced thermo-responsive (CIT) hydrogel with different properties compared to PNIPAM-based thermo-responsive hydrogels. The self-healing hydrogel with CIT properties could have great potential for application in areas related to bioscience, life simulation, and temperature switching.


2010 ◽  
Vol 43 (3) ◽  
pp. 1191-1194 ◽  
Author(s):  
Guohua Deng ◽  
Chuanmei Tang ◽  
Fuya Li ◽  
Huanfeng Jiang ◽  
Yongming Chen

Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1336
Author(s):  
Álvaro Miguel ◽  
Nuria García ◽  
Víctor Gregorio ◽  
Ana López-Cudero ◽  
Pilar Tiemblo

Polymer gel electrolytes have been prepared with polyethylene oxide (PEO) and the deep eutectic mixture of AlCl3: urea (uralumina), a liquid electrolyte which has proved to be an excellent medium for the electrodeposition of aluminum. The polymer gel electrolytes are prepared by mixing PEO in the liquid electrolyte at T > 65 °C, which is the melting point of PEO. This procedure takes a few minutes and requires no subsequent evaporation steps, being a solvent-free, and hence more sustainable procedure as compared to solvent-mediated ones. The absence of auxiliary solvents and evaporation steps makes their preparation highly reproducible and easy to scale up. PEO of increasing molecular weight (Mw = 1 × 105, 9 × 105, 50 × 105 and 80 × 105 g mol−1), including an ultra-high molecular weight (UHMW) polymer, has been used. Because of the strong interactions between the UHMW PEO and uralumina, self-standing gels can be produced with as little as 2.5 wt% PEO. These self-standing polymer gels maintain the ability to electrodeposit and strip aluminum, and are seen to retain a significant fraction of the current provided by the liquid electrolyte. Their gels’ rheology and electrochemistry are stable for months, if kept under inert atmosphere, and their sensitivity to humidity is significantly lower than that of liquid uralumina, improving their stability in the event of accidental exposure to air, and hence, their safety. These polymer gels are tough and thermoplastic, which enable their processing and molding into different shapes, and their recyclability and reprocessability. Their thermoplasticity also allows the preparation of concentrated batches (masterbatch) for a posteriori dilution or additive addition. They are elastomeric (rubbery) and very sticky, which make them very robust, easy to manipulate and self-healing.


2012 ◽  
Vol 05 ◽  
pp. 234-241 ◽  
Author(s):  
NAHID PIRHADY TAVANDASHTI ◽  
SOHRAB SANJABI

Nanostructured hybrid silica/epoxy films containing boehmite nanoparticles were investigated in the present work as pretreatments for AA2024 alloy. To produce the nanocomposite sol-gel films, boehmite nanoparticles prepared from hydrolysis/condensation of aluminum isopropoxide ( AlI ) were doped into another hybrid organosiloxane sol. The produced oxide nanoparticles have the capability to act as nanoreservoirs of corrosion inhibitors, releasing them controllably to protect the metallic substrate from corrosion. For this purpose the corrosion inhibitor, cerium nitrate, was introduced into the sol-gel system via loading the nanoparticles. The morphology and the structure of the hybrid sol-gel films were studied by Scanning Electron Microscopy (SEM). The corrosion protection properties of the films were investigated by Potentiodynamic Scanning (PDS) and Electrochemical Impedance Spectroscopy (EIS). The results show that the presence of boehmite nanoparticles highly improved the corrosion protection performance of the silica/epoxy coatings. Moreover, they can act as nanoreservoirs of corrosion inhibitors and provide prolonged release of cerium ions, offering a self-healing property to the film.


Author(s):  
J. A. N. Zasadzinski ◽  
R. K. Prud'homme

The rheological and mechanical properties of crosslinked polymer gels arise from the structure of the gel network. In turn, the structure of the gel network results from: thermodynamically determined interactions between the polymer chain segments, the interactions of the crosslinking metal ion with the polymer, and the deformation history of the network. Interpretations of mechanical and rheological measurements on polymer gels invariably begin with a conceptual model of,the microstructure of the gel network derived from polymer kinetic theory. In the present work, we use freeze-etch replication TEM to image the polymer network morphology of titanium crosslinked hydroxypropyl guars in an attempt to directly relate macroscopic phenomena with network structure.


Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 869
Author(s):  
Minghua Wei ◽  
Shaopeng Wu ◽  
Haiqin Xu ◽  
Hechuan Li ◽  
Chao Yang

Steel slag is the by-product of the steelmaking industry, the negative influences of which prompt more investigation into the recycling methods of steel slag. The purpose of this study is to characterize steel slag filler and study its feasibility of replacing limestone filler in asphalt concrete by evaluating the resistance of asphalt mastic under various aging methods. Firstly, steel slag filler, limestone filler, virgin asphalt, steel slag filler asphalt mastic and limestone filler asphalt mastic were prepared. Subsequently, particle size distribution, surface characterization and pore characterization of the fillers were evaluated. Finally, rheological property, self-healing property and chemical functional groups of the asphalt mastics with various aging methods were tested via dynamic shear rheometer and Fourier transform infrared spectrometer. The results show that there are similar particle size distributions, however, different surface characterization and pore characterization in the fillers. The analysis to asphalt mastics demonstrates how the addition of steel slag filler contributes to the resistance of asphalt mastic under the environment of acid and alkaline but is harmful under UV radiation especially. In addition, the pore structure in steel slag filler should be a potential explanation for the changing resistance of the asphalt mastics. In conclusion, steel slag filler is suggested to replace limestone filler under the environment of acid and alkaline, and environmental factor should be taken into consideration when steel slag filler is applied to replace natural fillers in asphalt mastic.


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