Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 62102, Taiwan.
Phys Chem Chem Phys. 2021 Sep 15;23(35):19269-19279. doi: 10.1039/d1cp02778f.
The multiscale structural and rheological features of a series of dilute and semidilute low-methoxyl (LM) pectin solutions and a representative pectin/calcium sol-gel sample were systematically explored using a comprehensive combination of dynamic (DLS) and static light/X-ray scattering (SALS/SLS/SAXS), rheology, and microscopy (OM/SEM) characterizations. The study focused on the rarely explored colloidal aspect of LM pectin solutions and sol-gel transition, in contrast to the polymeric features extensively explored in previous studies. A highly uniform colloid-like, micron-sized agglomerate species was revealed in dilute solutions, with a progressively increased degree of flocculation in the semidilute regime (≥1.5 wt%). The agglomerate species in these solutions was resolved to be formed by random associations of individual pectin chains ( = 30 nm, = 0.4 nm). Adding a critical amount of Ca (10 wt%) to a semidilute solution (2 wt%) has an instant and pronounced effect of enhancing the agglomerate flocculation and resulting in a locally jammed state. Meanwhile, the agglomerate interior underwent microstructural transformation, leading to hierarchical structures defined by intermediate (spherical) aggregate species ( ≈ 150 nm) and its packing cylindrical bundle ( ≈ 4 nm) composed of five pectin chains. Novel rheological features observed during the LM pectin/Ca sol-gel transition include the following: the dynamic modulus data exhibited excellent TTS (gelling time/relaxation time superposition) as previously observed for weakly attractive colloidal gels. Three yield points were noticed for the final gel sample, suggested to mark the bond breaking of the cluster network, cage breaking of the resulting jammed flocculates, and, eventually, breakup of a flocculate into smaller agglomerates with increasing stress amplitude.
采用动态光散射(DLS)和静态光/小角 X 射线散射(SALS/SLS/SAXS)、流变学和显微镜(OM/SEM)等综合手段,系统研究了一系列低甲氧基(LM)果胶稀溶液和半稀溶液以及代表性果胶/钙溶胶-凝胶样品的多尺度结构和流变特性。该研究侧重于 LM 果胶溶液和溶胶-凝胶转变的胶体方面,而不是以前研究中广泛探索的聚合物特性。在稀溶液中发现了高度均匀的类胶体、微米级聚集体,在半稀区(≥1.5wt%)中,絮凝程度逐渐增加。这些溶液中的聚集体被解析为由单个果胶链的随机缔合形成(=30nm,=0.4nm)。向半稀溶液(2wt%)中添加临界量的 Ca(10wt%)会立即显著增强聚集体的絮凝作用,导致局部形成堵塞状态。同时,聚集体内部发生微观结构转变,形成由中间(球形)聚集体(≈150nm)及其由五条果胶链组成的包装圆柱束(≈4nm)定义的分层结构。在 LM 果胶/Ca 溶胶-凝胶转变过程中观察到的新型流变特性包括:动态模量数据表现出优异的 TTS(凝胶时间/松弛时间叠加),如以前观察到的弱吸引力胶体凝胶一样。最终凝胶样品注意到三个屈服点,这可能标志着簇网络的键断裂、聚集体的笼状断裂,以及随着应力振幅的增加,聚集体破裂成更小的聚集体。