Strano Michael S, Moore Valerie C, Miller Michael K, Allen Mathew J, Haroz Erik H, Kittrell Carter, Hauge Robert H, Smalley R E
Center for Nanoscale Science and Technology, Rice University, Houston, Texas, USA.
J Nanosci Nanotechnol. 2003 Feb-Apr;3(1-2):81-6. doi: 10.1166/jnn.2003.194.
The ionic surfactant-assisted dispersion of single-walled carbon nanotubes in aqueous solution has been studied by Raman and fluorescent spectroscopy during ultrasonic processing. During the process, an equilibrium is established between free individuals and aggregates or bundles that limits the concentration of the former that is possible. This equilibrium is a function of free sodium dodecyl sulfate concentration. At surfactant concentrations below this value, fluorescence is shifted to a lower energy due to an increase in micropolarity from water association at the nanotube surface. The mechanism of dispersion is postulated as the formation of gaps or spaces at the bundle ends in the high shear environment of the ultrasonicated solution. Surfactant adsorption and diffusion then propagate this space along the bundle length, thereby separating the individual nanotube. The former is found to be controlling, with the use of a derived kinetic model for the dispersion process and extraction of the characteristic rate of nanotube isolation.
通过拉曼光谱和荧光光谱研究了离子表面活性剂辅助下单壁碳纳米管在水溶液中的超声分散过程。在此过程中,游离个体与聚集体或管束之间建立了一种平衡,这种平衡限制了游离个体可能达到的浓度。这种平衡是游离十二烷基硫酸钠浓度的函数。在表面活性剂浓度低于该值时,由于纳米管表面水缔合导致微极性增加,荧光会向较低能量偏移。分散机理被假定为在超声溶液的高剪切环境中,管束末端形成间隙或空间。然后表面活性剂的吸附和扩散沿着管束长度扩展这个空间,从而分离出单个纳米管。通过使用推导的分散过程动力学模型并提取纳米管分离的特征速率,发现前者起控制作用。