Division of Coating Technology and ‡Wallenberg Wood Science Center, School of Chemical Science and Engineering, Department of Fibre and Polymer Technology, KTH Royal Institute of Technology , SE-100 44 Stockholm, Sweden.
ACS Appl Mater Interfaces. 2017 Oct 11;9(40):35305-35318. doi: 10.1021/acsami.7b09009. Epub 2017 Sep 25.
In the present work, cellulose nanocrystals (CNCs) have been surface-modified either via covalent grafting or through physisorption of poly(n-butyl methacrylate) (PBMA) and employed as reinforcement in PCL. Covalent grafting was achieved by surface-initiated atom transfer radical polymerization (SI-ATRP). Two approaches were utilized for the physisorption: using either micelles of poly(dimethyl aminoethyl methacrylate)-block-poly(n-butyl methacrylate) (PDMAEMA-b-PBMA) or latex nanoparticles of poly(dimethyl aminoethyl methacrylate-co-methacrylic acid)-block-poly(n-butyl methacrylate) (P(DMAEMA-co-MAA)-b-PBMA). Block copolymers (PDMAEMA-b-PBMA)s were obtained by ATRP and subsequently micellized. Latex nanoparticles were produced via reversible addition-fragmentation chain-transfer (RAFT) mediated surfactant-free emulsion polymerization, employing polymer-induced self-assembly (PISA) for the particle formation. For a reliable comparison, the amounts of micelles/latex particles adsorbed and the amount of polymer grafted onto the CNCs were kept similar. Two different chain lengths of PBMA were targeted, below and above the critical molecular weight for chain entanglement of PBMA (M ∼ 56 000 g mol). Poly(ε-caprolactone) (PCL) nanocomposites reinforced with unmodified and modified CNCs in different weight percentages (0.5, 1, and 3 wt %) were prepared via melt extrusion. The resulting composites were evaluated by UV-vis, scanning electron microscopy (SEM), thermal gravimetric analysis (TGA), and tensile testing. All materials resulted in higher transparency, greater thermal stability, and stronger mechanical properties than unfilled PCL and nanocomposites containing unmodified CNCs. The degradation temperature of PCL reinforced with grafted CNCs was higher than that of micelle-modified CNCs, and the latter was higher than that of latex-adsorbed CNCs with a long PBMA chain length. The results clearly indicate that covalent grafting is superior to physisorption with regard to thermal and mechanical properties of the final nanocomposite. This unique study is of great value for the future design of CNC-based nanocomposites with tailored properties.
在本工作中,通过共价接枝或通过物理吸附聚(正丁基甲基丙烯酸酯)(PBMA)对纤维素纳米晶体(CNC)进行表面修饰,并将其用作 PCL 的增强材料。共价接枝通过表面引发原子转移自由基聚合(SI-ATRP)实现。为了物理吸附,采用了两种方法:使用聚(二甲基氨基乙基甲基丙烯酸酯)-嵌段-聚(正丁基甲基丙烯酸酯)(PDMAEMA-b-PBMA)的胶束或聚(二甲基氨基乙基甲基丙烯酸酯-共-甲基丙烯酸)-嵌段-聚(正丁基甲基丙烯酸酯)(P(DMAEMA-co-MAA)-b-PBMA)的乳胶纳米粒子。嵌段共聚物(PDMAEMA-b-PBMA)通过 ATRP 获得,随后胶束化。乳胶纳米粒子通过可逆加成-断裂链转移(RAFT)介导的无表面活性剂乳液聚合产生,采用聚合物诱导自组装(PISA)进行粒子形成。为了进行可靠的比较,吸附的胶束/乳胶粒子的量和接枝到 CNC 上的聚合物的量保持相似。目标是两种不同长度的 PBMA,低于和高于 PBMA 的链缠结临界分子量(M∼56000gmol)。通过熔融挤出制备了不同重量百分比(0.5、1 和 3wt%)的未改性和改性 CNC 增强的聚(ε-己内酯)(PCL)纳米复合材料。通过紫外-可见分光光度计、扫描电子显微镜(SEM)、热重分析(TGA)和拉伸测试对所得复合材料进行了评估。与未填充 PCL 和含有未改性 CNC 的纳米复合材料相比,所有材料均具有更高的透明度、更大的热稳定性和更强的机械性能。接枝 CNC 增强的 PCL 的降解温度高于胶束改性 CNC,而后者高于具有长 PBMA 链长的乳胶吸附 CNC。结果清楚地表明,与最终纳米复合材料的热和机械性能相比,共价接枝优于物理吸附。这项独特的研究对于未来设计具有定制性能的基于 CNC 的纳米复合材料具有重要价值。