“…The mass loss curve indicated two major stages. The first stage of mass loss occurred at around 200 °C corresponding to the evaporation of a small amount of adsorbed water and solvent (Mao et al 2015 ; Zhong et al 2015 ), while the second stage was the decomposition of SD-SEAL structures at around 380 °C, indicating that the newly synthesized products were highly temperature resistant, which was attributed to the presence of benzene in the SD-SEAL (Luo et al 2016 ; Hu et al 2016 ). Fig.…”
Emulsifier-free poly(methyl methacrylate–styrene) [P(MMA–St)] nanospheres with an average particle size of 100 nm were synthesized in an isopropyl alcohol–water medium by a solvothermal method. Then, through radical graft copolymerization of thermo-sensitive monomer N-isopropylacrylamide (NIPAm) and hydrophilic monomer acrylic acid (AA) onto the surface of P(MMA–St) nanospheres at 80 °C, a series of thermo-sensitive polymer nanospheres, named SD-SEAL with different lower critical solution temperatures (LCST), were prepared by adjusting the mole ratio of NIPAm to AA. The products were characterized by Fourier transform infrared spectroscopy, transmission electron microscopy, thermogravimetric analysis, particle size distribution, and specific surface area analysis. The temperature-sensitive behavior was studied by light transmittance tests, while the sealing performance was investigated by pressure transmission tests with Lungmachi Formation shales. The experimental results showed that the synthesized nanoparticles are sensitive to temperature and had apparent LCST values which increased with an increase in hydrophilic monomer AA. When the temperature was higher than its LCST value, SD-SEAL played a dual role of physical plugging and chemical inhibition, slowed down pressure transmission, and reduced shale permeability remarkably. The plugged layer of shale was changed to being hydrophobic, which greatly improved the shale stability
“…The mass loss curve indicated two major stages. The first stage of mass loss occurred at around 200 °C corresponding to the evaporation of a small amount of adsorbed water and solvent (Mao et al 2015 ; Zhong et al 2015 ), while the second stage was the decomposition of SD-SEAL structures at around 380 °C, indicating that the newly synthesized products were highly temperature resistant, which was attributed to the presence of benzene in the SD-SEAL (Luo et al 2016 ; Hu et al 2016 ). Fig.…”
Emulsifier-free poly(methyl methacrylate–styrene) [P(MMA–St)] nanospheres with an average particle size of 100 nm were synthesized in an isopropyl alcohol–water medium by a solvothermal method. Then, through radical graft copolymerization of thermo-sensitive monomer N-isopropylacrylamide (NIPAm) and hydrophilic monomer acrylic acid (AA) onto the surface of P(MMA–St) nanospheres at 80 °C, a series of thermo-sensitive polymer nanospheres, named SD-SEAL with different lower critical solution temperatures (LCST), were prepared by adjusting the mole ratio of NIPAm to AA. The products were characterized by Fourier transform infrared spectroscopy, transmission electron microscopy, thermogravimetric analysis, particle size distribution, and specific surface area analysis. The temperature-sensitive behavior was studied by light transmittance tests, while the sealing performance was investigated by pressure transmission tests with Lungmachi Formation shales. The experimental results showed that the synthesized nanoparticles are sensitive to temperature and had apparent LCST values which increased with an increase in hydrophilic monomer AA. When the temperature was higher than its LCST value, SD-SEAL played a dual role of physical plugging and chemical inhibition, slowed down pressure transmission, and reduced shale permeability remarkably. The plugged layer of shale was changed to being hydrophobic, which greatly improved the shale stability
“…To realize the promotion of ionic concentration, an effective approach is to change the original linear structure of polymers into the topology branching structure for transporting more lithiumions in the same conditions. [27,28] In this regard, nonlinear topological polymers are appealing alternative SPE matrices of linear polymers owing to its incomparable advantages. The nonlinear topological structure is rich in functional groups, which can provide more binding sites to dissolve lithium salts.…”
Solid polymer electrolytes (SPEs) are still being considered as a candidate to replace liquid electrolytes for high‐safety and flexible lithium batteries due to their superiorities including light‐weight, good flexibility, and shape versatility. However, inefficient ion transportation of linear polymer electrolytes is still the biggest challenge. To improve ion transport capacity, developing novel polymer electrolytes are supposed to be an effective strategy. Nonlinear topological structures such as hyperbranched, star‐shaped, comb‐like, and brush‐like types have highly branched features. Compared with linear polymer electrolytes, topological polymer electrolytes possess more functional groups, lower crystallization, glass transition temperature, and better solubility. Especially, a large number of functional groups are beneficial to dissociation of lithium salt for improving the ion conductivity. Furthermore, topological polymers have strong design ability to meet the requirements of comprehensive performances of SPEs. In this review, the recent development in topological polymer electrolytes is summarized and their design thought is analyzed. Outlooks are also provided for the development of future SPEs. It is expected that this review can raise a strong interest in the structural design of advanced polymer electrolyte, which can give inspirations for future research on novel SPEs and promote the development of next‐generation high‐safety flexible energy storage devices.
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