Wen Yu Ho, Schaefer Jennifer L, Archer Lynden A
School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.
ACS Macro Lett. 2015 Jan 20;4(1):119-123. doi: 10.1021/mz5006662. Epub 2015 Jan 7.
The linear viscoelastic (LVE) spectrum of a soft colloidal glass is accessed with the aid of a time-concentration superposition (TCS) principle, which unveils the glassy particle dynamics from in-cage rattling motion to out-of-cage relaxations over a broad frequency range 10 rad/s < ω < 10 rad/s. Progressive dilution of a suspension of hairy nanoparticles leading to increased intercenter distances is demonstrated to enable continuous mapping of the structural relaxation for colloidal glasses. In contrast to existing empirical approaches proposed to extend the rheological map of soft glassy materials, i.e., time-strain superposition (TSS) and strain-rate frequency superposition (SRFS), TCS yields a LVE master curve that satisfies the Kramers-Kronig relations which interrelate the dynamic moduli for materials at equilibrium. The soft glassy rheology (SGR) model and literature data further support the general validity of the TCS concept for soft glassy materials.
借助时间-浓度叠加(TCS)原理,可获取软胶体玻璃的线性粘弹性(LVE)光谱,该原理揭示了在10⁻⁴ rad/s < ω < 10² rad/s的宽频率范围内,玻璃态颗粒从笼内晃动运动到笼外弛豫的动力学过程。研究表明,对毛发状纳米颗粒悬浮液进行逐步稀释,导致中心间距增大,能够实现对胶体玻璃结构弛豫的连续映射。与为扩展软玻璃态材料流变学图谱而提出的现有经验方法,即时-应变叠加(TSS)和应变速率-频率叠加(SRFS)不同,TCS产生的LVE主曲线满足相互关联平衡态材料动态模量的Kramers-Kronig关系。软玻璃态流变学(SGR)模型和文献数据进一步支持了TCS概念对软玻璃态材料的普遍有效性。