Comparison of nanocomposite dispersion and distribution for several melt mixers. (13th March 2023)

• Record Type: Journal Article
• Authors: Veigel, Danielle; Rishi, Kabir; Okoli, Ugochukwu; Beaucage, Gregory; Galloway, Jeffrey A.; Campanelli, Hannah; Ilavsky, Jan; Kuzmenko, Ivan; Fickenscher, Melodie
• Is Part Of: Polymer. Volume 269(2023)
• Publication Date: 2023-03-13
• Subjects: Nanocomposite -- Ultra-small-angle X-ray scattering -- Accumulated strain -- Co-rotating twin-screw extruder -- Carbon black -- Polystyrene -- Single screw extruder -- Banbury mixer -- Laminar -- Turbulent -- Reynolds number; Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; 547.7
• DOI: 10.1016/j.polymer.2023.125735
• Languages: English
• ISSNs: 0032-3861

Abstract

Abstract: Breakup (dispersion) and distribution of nanoparticles are the chief hurdles towards taking advantage of nanoparticles in polymer nanocomposites for reinforcement, flame retardancy, conductivity, chromaticity, and other properties. Microscopy is often used to quantify mixing, but it has a limited field of view, does not average over bulk samples, and fails to address nano-particle hierarchical structures. Ultra-small-angle X-ray scattering (USAXS) can provide a macroscopic statistical average of nanoscale dispersion (breakup) and emergent hierarchical structure, as well as the distribution on the nanoscale. This work compares several common mixer geometries for carbon black-polystyrene nanocomposites. Two twin-screw extruder geometries, typical for industrial processing of melt blends, are compared with a laboratory-scale single screw extruder and a Banbury mixer. It is found that for a given mixer, nanoscale distribution increases following a van der Waals function using accumulated strain as an analogue for temperature while macroscopic distribution/dispersion, using microscopy, does not follow this dependency. Breakup and aggregation in dispersive mixing follow expected behavior on the nanoscale. Across these drastically different mixing geometries an unexpected dependency is observed for nanoscale distributive mixing (both nano and macroscopic) as a function of accumulated strain that may reflect a transition from distributive turbulent to dispersive laminar mixing as the mixing gap is reduced. Graphical abstract: Image 1 Highlights: Nanoparticle dispersion/distribution is controlled by mixing geometry and accumulated strain. Nanocomposites of carbon black in polystyrene studied using twin and single screw extruders and a Banbury mixer. Small-angle X-ray scattering (virial/Van der Waals model) and SEM characterized mixing. Dispersive/breakup may arise in narrow gap/laminar flow; distributive mixing in wider gap/turbulent flow. Mixing changes in carbon black hierarchical structure are described.