These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Stick-slip phenomenon in measurements of dynamic contact angles and surface viscoelasticity of poly(styrene-b-isoprene-b-styrene) triblock copolymers.
    Author: Zuo B, Zheng FF, Zhao YR, Chen T, Yan ZH, Ni H, Wang X.
    Journal: Langmuir; 2012 Mar 06; 28(9):4283-92. PubMed ID: 22329614.
    Abstract:
    In this paper, a series of poly(styrene-b-isoprene-b-styrene) triblock copolymers (SIS), with different chemical components, was synthesized by anionic polymerization. The relationships between surface structures of these block copolymers and their stick-slip phenomena were investigated. There is a transition from stick-slip to a closely smooth motion for the SIS films with increasing PS content; the patterns almost vanish and the three-phase line appears to move overall smoothly on the film surface. The results show that the observed stick-slip pattern is strongly dependent on surface viscoelasticity. The jumping angle Δθ, which is defined as θ(1) - θ(2) (when a higher limit to θ(1) is obtained, the triple line "jumps" from θ(1) to θ(2) with increases in drop volume), was employed to scale the stick-slip behavior on various SIS film surfaces. Scanning force microscopy/atomic force microscopy (AFM) and sum frequency generation methods were used to investigate the surface structures of the films and the contributions of various possible factors to the observed stick-slip behavior. It was found that there is a linear relationship between jumping angle Δθ and the slope of the approach curve obtained from AFM force measurement. This means that the stick-slip behavior may be attributed mainly to surface viscoelasticity for SIS block copolymers. The measurement of jumping angle Δθ may be a valuable method for studying surface structure relaxation of polymer films.
    [Abstract] [Full Text] [Related] [New Search]