Liang Shuhua, Wang Xinyu, Chen Liheng, Qiu Xueqing
Guangdong Provincial Key Laboratory of Plant Resources Biorefinery, School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China.
Guangdong Provincial Key Laboratory of Plant Resources Biorefinery, School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China; Guangdong Provincial Laboratory of Chemistry and Fine Chemical Engineering Jieyang Center, Jieyang 515200, China; Guangdong Basic Research Center of Excellence for Ecological Security, Green Development in Guangdong-Hong Kong-Marco Greater Bay Area (GBA), Guangdong University of Technology, Guangzhou 510006, China.
J Colloid Interface Sci. 2025 Apr;683(Pt 1):833-840. doi: 10.1016/j.jcis.2024.12.128. Epub 2024 Dec 18.
Fatty acids, in particular, are valued as phase change materials (PCMs) for their non-toxic, biodegradable nature and thermal stability. However, the leakage and supercooling issues during phase transitions limit their application. Microencapsulation of PCMs, while improving thermal response, often leads to supercooling, complicating temperature regulation and increasing energy consumption. Lignin, a renewable biomass resource, offers potential as a shell material for PCM encapsulation. To address compatibility issues between lignin and fatty acids, we modified lignin via acetylation and prepared hybrid acetylated lignin-stearic acid capsules (hyb-ACLSCs) using an anti-solvent method. Density functional theory (DFT) revealed that acetylated lignin exhibits stronger interactions with fatty acids, leading to higher particle yields (40.8 %), enhanced fatty acid loading (57.2 %) with a high phase-transition temperature of about 70 ℃, and improved phase transition behavior with a stable latent heat of about 250 J/g after 50 heating-cooling cycles. The heterogeneity of lignin facilitated multi-hierarchical self-assembly, preventing supercooling and enabling the formation of nano-sized phase change materials. The resulting hybrid capsules demonstrated high latent heat, negligible supercooling, and are highly promising for energy storage applications.
脂肪酸因其无毒、可生物降解的特性和热稳定性,尤其被视为相变材料(PCM)。然而,相变过程中的泄漏和过冷问题限制了它们的应用。相变材料的微胶囊化虽然改善了热响应,但往往会导致过冷,使温度调节变得复杂并增加能耗。木质素作为一种可再生生物质资源,具有作为相变材料封装壳材料的潜力。为了解决木质素与脂肪酸之间的相容性问题,我们通过乙酰化对木质素进行改性,并采用反溶剂法制备了乙酰化木质素-硬脂酸混合胶囊(hyb-ACLSCs)。密度泛函理论(DFT)表明,乙酰化木质素与脂肪酸表现出更强的相互作用,从而导致更高的颗粒产率(40.8%)、更高的脂肪酸负载量(57.2%),其相变温度约为70℃,且在50次加热-冷却循环后,相变行为得到改善,潜热稳定在约250J/g。木质素的异质性促进了多级自组装,防止了过冷,并使得纳米级相变材料得以形成。所得的混合胶囊具有高潜热、可忽略的过冷现象,在储能应用方面极具前景。