University of Illinois Urbana-Champaign

Role of surface chemistry in sub-Einstein rheology of nano-composites

Ranka, Moulik

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Ranka_Moulik.pdf

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https://hdl.handle.net/2142/34404

Description

Title
Role of surface chemistry in sub-Einstein rheology of nano-composites
Author(s)
Ranka, Moulik
Issue Date
2012-09-18T21:15:17Z
Director of Research (if dissertation) or Advisor (if thesis)
Zukoski, Charles F.
Department of Study
Chemical & Biomolecular Engr
Discipline
Chemical Engineering
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
M.S.
Degree Level
Thesis
Date of Ingest
2012-09-18T21:15:17Z
Keyword(s)
  • polyhedral oligomeric silisequioxane (POSS)
  • Rheology
  • Nano-Composite
  • Intrinsic Viscosity
Abstract
Sub-Einstein and negative intrinsic viscosities resulting from the addition of nano-fillers to polymer melts approximately 2-10 nm diameter have been reported. Here we explore the intrinsic viscosity of polyhedral oligomeric silisequioxane (POSS) particles of approximately 1.6-2.5 nm diameters as a function of polymer molecular weight. These nanoparticles consist of cubes of 8-corner silicon atoms edge bridged with oxygen atoms. A variety of functional groups are attached to the corner silicon atoms. Three different POSS particles are explored: POSS with 8 tethered alkyl chains (butyl and octyl) and POSS with 8 tethered polyethylene glycol, PEG, chains of degree of polymerization, n ~ 13 segments. The tethered particles are dissolved in a homopolymer matrix (polydimethyl siloxane, PDMS, for octyl-POSS and butyl-POSS and PEG for PEG-POSS). The POSS intrinsic viscosity drops with increasing polymer matrix molecular weight from approximately 2.5 (as predicted by Einstein for no slip boundary conditions) to negative values. We discuss these results in light of previous studies of the intrinsic viscosity of nanoparticles in polymer melts with special attention to particle-polymer segment surface interactions that result in particle-polymer miscibility and ideas based on the ability of nanoparticles to alter polymer relaxation rates. We develop a hypothesis that negative intrinsic viscosities are associated with weak particle-polymer segment surface interactions while at the same time developing mechanisms that ensure particles remain soluble in the polymer melt.
Graduation Semester
2012-08
Permalink
http://hdl.handle.net/2142/34404
Copyright and License Information
Copyright 2012 Moulik Ranka

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