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Silica nanoparticles-coated poly(glycidyl methacrylate-ethylene dimethacrylate) co-polymer beads containing organic phase change materials

机译:包含有机相变材料的二氧化硅纳米颗粒涂层的聚(甲基丙烯酸缩水甘油酯-二甲基丙烯酸乙烯酯)共聚物微珠

摘要

Macroporous sorbent beads of large and small sizes were prepared by the AIBN-initiated suspension radical polymerization of glycidyl methacrylate and ethylene dimethacrylate monomers in the presence of an inert porogen. The large and small microspheres were loaded with paraffin and cetyl alcohol PCMs, respectively, and coated with silica nanoparticles after sol-gel synthesis of trimethoxy(methyl)silane hydrolysate. The energy storing capacity of the form-stabilized PCM containing composite particles was monitored by differential scanning calorimetry. Accelerated thermal cycling tests were carried out to determine the thermal reliability of the microencapsulated PCMs. Paraffin and cetyl alcohol content of the microcapsules was 42.9 % and 48.9 %, respectively. The microcomposites with higher PCM content showed correspondingly higher latent heat storage capacity (melting and solidification enthalpies were 96.1 J/g and 94.7 J/g). However, there was low enthalpy change observed after 1000 thermal cycles of cetyl alcohol containing capsules, which indicated that its leakage from the microcomposites was not substantial.
机译:在惰性成孔剂的存在下,通过AIBN引发的甲基丙烯酸缩水甘油酯和二甲基丙烯酸乙二酯单体的悬浮自由基聚合反应,制备了大小不同的大孔吸附珠。大和小微球分别装有石蜡和鲸蜡醇PCM,并在溶胶-凝胶法合成三甲氧基(甲基)硅烷水解产物后用二氧化硅纳米粒子包被。通过差示扫描量热法监测含有形状稳定的PCM的复合颗粒的储能能力。进行了加速的热循环测试,以确定微囊PCM的热可靠性。微胶囊的石蜡和鲸蜡醇含量分别为42.9%和48.9%。具有较高PCM含量的微复合材料显示出相应较高的潜热储存能力(熔融和凝固焓为96.1J / g和94.7J / g)。但是,在含有鲸蜡醇的胶囊进行1000次热循环后,观察到的焓变较低,这表明其从微复合材料中泄漏的可能性不大。

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