Preparation method of interpenetrating network formed phase-change material
An interpenetrating network and phase change material technology, which is applied in the field of aliphatic polymer compounds and their preparation, can solve the problem that no temperature-adjusting fibers and fabrics have been found for shape-changing phase change materials, thermosetting polymers lose their phase change heat storage capacity, and cross-phase It is difficult to control the connection density and other problems, so as to achieve the effect of excellent setting effect, good strength and low production cost.
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Embodiment 1
[0029] Accurately weigh 4g of network monomer N-methylolacrylamide (NHMPA), 0.6g of cross-linking agent N,N-methylene bisacrylamide (BIS), 18.9g of phase change material polyethylene glycol (PEG2000), Add 24ml of distilled water into a flat-bottomed flask, and after dissolving, ultrasonically disperse for 5 minutes, then add initiator ammonium persulfate (APS) 0.12g, and continue ultrasonically dispersing for 5 minutes, so that the large and small molecules in the solution are mixed evenly. React at 75°C for 3 hours to generate a synchronous interpenetrating network hydrogel. The prepared gel was put into an electric heating constant temperature blast drying oven and dried to a constant weight to obtain an interpenetrating network shape-setting phase change material.
[0030] The prepared interpenetrating network shape-setting phase change material is tested for thermal insulation, and passed through the step cooling curve (see figure 1 ) analysis shows that the phase change ...
Embodiment 2
[0035] Accurately weigh 4g of network monomer N-methylolacrylamide (NHMPA), 0.8g of cross-linking agent N,N-methylene bisacrylamide (BIS), 11.3g of phase change material polyethylene glycol (PEG2000), Add 24ml of distilled water into a flat-bottomed flask, and after dissolving, ultrasonically disperse for 5 minutes, then add 0.1g of initiator ammonium persulfate (APS), and continue ultrasonically dispersing for 5 minutes, so that the large and small molecules in the solution are evenly mixed. The reaction was carried out at 75°C for 3 hours to generate a synchronous interpenetrating network polymer. The prepared polymer is put into an electric heating constant temperature blast drying oven and dried to a constant weight to obtain an interpenetrating network shape-setting phase change material.
Embodiment 3
[0037] Accurately weigh 4g of the network monomer N-methylolacrylamide (NHMPA), 0.6g of the cross-linking agent N,N-methylene bisacrylamide (BIS), 18.5g of the phase change material polyethylene glycol (PEG4000), Add 40ml of distilled water into a flat-bottomed flask, and after dissolving, ultrasonically disperse for 5 minutes, then add 0.08g of initiator ammonium persulfate (APS), and continue ultrasonically dispersing for 5 minutes, so that the large and small molecules in the solution are evenly mixed. React at 80°C for 3.5 hours to generate a synchronous interpenetrating network hydrogel. The prepared gel was put into an electric heating constant temperature blast drying oven and dried to a constant weight to obtain an interpenetrating network shape-setting phase change material.
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