Hipulan Louell Nikki A, Dingcong Roger G, Estrada Dave Joseph E, Dumancas Gerard G, Bondaug John Christian S, Alguno Arnold C, Bacosa Hernando P, Malaluan Roberto M, Lubguban Arnold A
Center for Sustainable Polymers, Mindanao State University - Iligan Institute of Technology, A. Bonifacio Avenue, Iligan9200, Philippines.
Environmental Science Graduate Program, Department of Biological Sciences, Mindanao State University - Iligan Institute of Technology, A. Bonifacio Avenue, Iligan 9200, Philippines.
ACS Omega. 2024 Mar 7;9(11):13112-13124. doi: 10.1021/acsomega.3c09598. eCollection 2024 Mar 19.
The utilization of coconut diethanolamide (-CDEA) as a substitute polyol for petroleum-based polyol in fully biobased rigid polyurethane-urea foam (RPUAF) faces challenges due to its short chain and limited cross-linking capability. This leads to compromised cell wall resistance during foam expansion, resulting in significant ruptured cells and adverse effects on mechanical and thermal properties. To address this, a novel sequential amidation-prepolymerization route was employed on coconut oil, yielding a hydroxyl-terminated poly(urethane-urea) prepolymer polyol (COPUAP). Compared to -CDEA, COPUAP exhibited a decreased hydroxyl value (496.3-473.2 mg KOH/g), an increase in amine value (13.464-24.561 mg KOH/g), and an increase in viscosity (472.4-755.8 mPa·s), indicating enhanced functionality of 34.3 mgKOH/g and chain lengthening. Further, COPUAP was utilized as the sole B-side polyol in the production of RPUAF (PU-COPUAP). The improved functionality of COPUAP and its improved cross-linking capability during foaming have significantly improved cell morphology, resulting in a remarkable 4.7-fold increase in compressive strength (132-628 kPa), a 3.5-fold increase in flexural strength (232-828 kPa), and improved insulation properties with a notable decrease in thermal conductivity (48.02-34.52 mW/m·K) compared to PU-CDEA in the literature. Additionally, PU-COPUAP exhibited a 16.5% increase in the water contact angle (114.93° to 133.87°), attributing to the formation of hydrophobic biuret segments and a tightly packed, highly cross-linked structure inhibiting water penetration. This innovative approach sets a new benchmark for fully biobased rigid foam production, delivering high load-bearing capacity, exceptional insulation, and significantly improved hydrophobicity.
在全生物基硬质聚氨酯-脲泡沫(RPUAF)中,使用椰子二乙醇酰胺(-CDEA)作为石油基多元醇的替代多元醇面临挑战,因为其链短且交联能力有限。这导致泡沫膨胀过程中细胞壁抗性受损,从而产生大量破裂细胞,并对机械和热性能产生不利影响。为了解决这个问题,采用了一种新颖的顺序酰胺化-预聚合路线处理椰子油,得到了一种端羟基聚(聚氨酯-脲)预聚物多元醇(COPUAP)。与-CDEA相比,COPUAP的羟值降低(496.3 - 473.2 mg KOH/g),胺值增加(13.464 - 24.561 mg KOH/g),粘度增加(472.4 - 755.8 mPa·s),表明官能度提高了34.3 mgKOH/g且链增长。此外,COPUAP被用作生产RPUAF(PU-COPUAP)的唯一B侧多元醇。COPUAP官能度的提高及其在发泡过程中改善的交联能力显著改善了泡孔形态,与文献中的PU-CDEA相比,抗压强度显著提高了4.7倍(132 - 628 kPa),抗弯强度提高了3.5倍(232 - 828 kPa),并且隔热性能得到改善,热导率显著降低(48.02 - 34.52 mW/m·K)。此外,PU-COPUAP的水接触角增加了16.5%(从114.93°增加到133.87°),这归因于疏水缩二脲链段的形成以及紧密堆积、高度交联的结构抑制了水的渗透。这种创新方法为全生物基硬质泡沫生产树立了新标杆,具有高承载能力、出色的隔热性能以及显著改善的疏水性。