High-strength ionic liquid gel and preparation method thereof
An ionic liquid and ionic liquid solvent technology, applied in the field of high-strength ionic liquid gel and its preparation, can solve the problem of insignificant improvement of mechanical properties of ionic liquid gel, achieve excellent self-healing performance, broad application prospects, and improve mechanical properties. performance effect
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Embodiment 1-16
[0062] Add physical cross-linking monomer, ionic liquid monomer, dispersing monomer, initiator and ionic liquid solvent into the flask, fully stir and dissolve at room temperature. The mixed solution was deoxygenated and injected into a pre-prepared glass mold through a syringe, and cured under ultraviolet light (365nm wavelength, 8W) for 2h to obtain an ionic liquid gel. The specific substances and amounts used in the physical crosslinking monomer, ionic liquid monomer, dispersing monomer and ionic liquid solvent are shown in Table 1. The initiators are all 2-hydroxy-4-(2-hydroxyethoxy)-2-methylpropiophenone, and the concentration of the initiator in the ionic liquid solvent is 0.00625g / mL.
[0063] Raw materials and proportioning of table 1 embodiment 1-16
[0064]
[0065]
[0066] Performance tests were performed on the ionic liquid gels of Examples 1-16.
[0067] 1.1 Gel mechanical properties test
[0068] Test method: Use a 2mm thick mold to prepare the ionic li...
Embodiment 3
[0074] With embodiment 3 ( figure 1 )AAm / [VBIm][BF 4 ] / DMAA / [BMIm][BF 4 ] system as an example, dissolved in deuterated DMSO after polymerization at different times, and monitored the monomer conversion process by Bruker 400MHz DRX spectrometer. where [VBIm][BF 4 ], the double bond characteristic peak is located at 7.2-7.4ppm, the double bond characteristic peak of DMAA is located at 6.7-6.9ppm, and the characteristic peak of AAm is located at 5.55-5.7ppm, which can be obtained by referring to the ionic liquid [BMIm][BF 4 ] The methyl peak area on the alkyl chain was calculated to obtain the conversion data. Such as figure 1 As shown, in the initial stage of polymerization, the conversion rates of DMAA and AAm are higher than that of [VBIm][BF 4 ], forming polymer chains with higher crosslink density. As the polymerization proceeds, the proportion of unreacted DMAA and AAm in the system decreases, [VBIm][BF 4 ] The proportion of monomers increases instead, so polymer ch...
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