Beyond diffusion-limited aggregation kinetics in microparticle suspensions

Randall M. Erb, Melissa D. Krebs, Eben Alsberg, Bappaditya Samanta, Vincent M. Rotello, and Benjamin B. Yellen
Phys. Rev. E 80, 051402 – Published 2 November 2009

Abstract

Aggregation in nondiffusion limited colloidal particle suspensions follows a temporal power-law dependence that is consistent with classical diffusion limited cluster aggregation models; however, the dynamic scaling exponents observed in these systems are not adequately described by diffusion limited cluster aggregation models, which expect these scaling exponents to be constant over all experimental conditions. We show here that the dynamic scaling exponents for 10μm particles increase with the particle concentration and the particle-particle free energy of interaction. We provide a semiquantitative explanation for the scaling behavior in terms of the long-ranged particle-particle interaction potential.

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  • Received 3 May 2009

DOI:https://doi.org/10.1103/PhysRevE.80.051402

©2009 American Physical Society

Authors & Affiliations

Randall M. Erb1,*, Melissa D. Krebs2, Eben Alsberg2, Bappaditya Samanta3, Vincent M. Rotello3, and Benjamin B. Yellen1

  • 1Mechanical Engineering and Materials Science, Center for Biologically Inspired Materials and Material Systems, Duke University, Durham, North Carolina 27708, USA
  • 2Department of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio 44106, USA
  • 3Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, USA

  • *Mailing address: Duke University, 144 Hudson Hall, Durham, NC, 27708, USA. FAX: (919)-660-8963; randall.erb@duke.edu

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Vol. 80, Iss. 5 — November 2009

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