Capuano, Guglielmo (2011) STRUCTURE AND DYNAMICS OF MODEL POLYMER NANOCOMPOSITES. [Tesi di dottorato] (Unpublished)

[img] PDF
CAPUANO_GUGLIELMO.pdf
Visibile a [TBR] Repository staff only fino a 20 December 2015.

Download (5MB)
Item Type: Tesi di dottorato
Language: English
Title: STRUCTURE AND DYNAMICS OF MODEL POLYMER NANOCOMPOSITES
Creators:
CreatorsEmail
Capuano, Guglielmoguglielmo.capuano@unina.it
Date: 30 November 2011
Number of Pages: 103
Institution: Università degli Studi di Napoli Federico II
Department: Ingegneria dei materiali e della produzione
Doctoral School: Ingegneria industriale
PHD name: Ingegneria dei materiali e delle strutture
PHD cycle: 24
PHD Coordinator:
nameemail
Mensitieri, Giuseppemensitie@unina.it
Tutor:
nameemail
Acierno, Domenicoacierno@unina.it
Date: 30 November 2011
Number of Pages: 103
Uncontrolled Keywords: polymer nanocomposites, silica, rheology
MIUR S.S.D.: Area 09 - Ingegneria industriale e dell'informazione > ING-IND/22 - Scienza e tecnologia dei materiali
Date Deposited: 13 Dec 2011 11:20
Last Modified: 30 Apr 2014 19:48
URI: http://www.fedoa.unina.it/id/eprint/8830

Abstract

We study the structure and linear viscoelasticity of interacting polymer-nanocomposites based on mixtures of polyethylene-oxide and fumed silica particles. The filler is dispersed within the polymer using different techniques which lead to different dispersion states. The analysis of the dynamic response of our systems, highlights the formation of a stress-bearing network above a critical volume fraction, Фc. Extending a two-phase model used to describe weakly interacting systems, we show that above Фc the melt-state elasticity of the composites arises from the independent contributions of a polymer-particle network and a viscous matrix. We also find that while Фc depends on the initial state of dispersion, the network elasticity scales with volume fraction following a universal power-law, with an exponent ν≈1.8. Such scaling law has been recently predicted for the stress-bearing mechanism governed by polymer-mediated interactions.

Actions (login required)

View Item View Item