Voronin Denis V, Sitmukhanova Eliza, Mendgaziev Rais I, Rubtsova Maria I, Kopitsyn Dmitry, Cherednichenko Kirill A, Semenov Anton P, Fakhrullin Rawil, Shchukin Dmitry G, Vinokurov Vladimir
Department of Physical and Colloid Chemistry, National University of Oil and Gas "Gubkin University", 119991 Moscow, Russia.
Institute of Fundamental Medicine and Biology, Kazan Federal University, Kreml uramı 18, 42000 Kazan, Republic of Tatarstan, Russia.
Materials (Basel). 2023 Sep 28;16(19):6460. doi: 10.3390/ma16196460.
Organic phase-change materials (PCMs) hold promise in developing advanced thermoregulation and responsive energy systems owing to their high latent heat capacity and thermal reliability. However, organic PCMs are prone to leakages in the liquid state and, thus, are hardly applicable in their pristine form. Herein, we encapsulated organic PCM -Octadecane into polyurethane capsules via polymerization of commercially available polymethylene polyphenylene isocyanate and polyethylene glycol at the interface oil-in-water emulsion and studied how various -Octadecane feeding affected the shell formation, capsule structure, and latent heat storage properties. The successful shell polymerization and encapsulation of -Octadecane dissolved in the oil core was verified by confocal microscopy and Fourier-transform infrared spectroscopy. The mean capsule size varied from 9.4 to 16.7 µm while the shell was found to reduce in thickness from 460 to 220 nm as the -Octadecane feeding increased. Conversely, the latent heat storage capacity increased from 50 to 132 J/g corresponding to the growth in actual -Octadecane content from 25% to 67% as revealed by differential scanning calorimetry. The actual -Octadecane content increased non-linearly along with the -Octadecane feeding and reached a plateau at 66-67% corresponded to 3.44-3.69 core-to-monomer ratio. Finally, the capsules with the reasonable combination of structural and thermal properties were evaluated as a thermoregulating additive to a commercially available paint.
有机相变材料(PCM)由于其高潜热容量和热可靠性,在开发先进的温度调节和响应式能量系统方面具有广阔前景。然而,有机PCM在液态时容易泄漏,因此很难以其原始形式应用。在此,我们通过在水包油乳液界面将市售的聚亚甲基多苯基异氰酸酯和聚乙二醇聚合,将有机PCM十八烷封装到聚氨酯胶囊中,并研究了不同的十八烷进料量如何影响壳层形成、胶囊结构和潜热存储性能。通过共聚焦显微镜和傅里叶变换红外光谱验证了溶解在油核中的十八烷的壳层成功聚合和封装。随着十八烷进料量的增加,平均胶囊尺寸从9.4微米变化到16.7微米,而壳层厚度从460纳米减小到220纳米。相反,差示扫描量热法显示,潜热存储容量从50焦耳/克增加到132焦耳/克,对应于实际十八烷含量从25%增长到67%。实际十八烷含量随着十八烷进料量非线性增加,并在66 - 67%达到平台期,对应于3.44 - 3.69的核与单体比例。最后,对具有合理结构和热性能组合的胶囊作为市售涂料的温度调节添加剂进行了评估。