APS March Meeting 2010
Volume 55, Number 2
Monday–Friday, March 15–19, 2010;
Portland, Oregon
Session V5: Industrial Applications of Neutron Scattering
8:00 AM–11:00 AM,
Thursday, March 18, 2010
Room: Portland Ballroom 256
Sponsoring
Units:
DCMP FIAP
Chair: Michael Crawford, DuPont
Abstract ID: BAPS.2010.MAR.V5.5
Abstract: V5.00005 : Why Particle Dispersions Matter: Product Discovery and Problem Solving in the Hydrocarbon Industry Through Neutron Scattering*
10:24 AM–11:00 AM
Preview Abstract
Abstract
Author:
Hubert King
(ExxonMobil Research and Eng. Co.)
A surprisingly wide range of matter consists of dispersions of one material
in another. In the hydrocarbon industry we often work with mixtures of
solid, liquid, and gas as a consequence of the production of hydrocarbons.
For example, in deep sea oil production solid phases of wax or gas hydrates
can form in pipelines due to low temperatures and high pressures.
Dispersions also arise in the products we design; examples include polymers,
fuel additives, and lubricants. Hence, understanding such dispersions is a
key technology. Size of the dispersed phase (supermolecular) and sensitivity
of the structure to the presence of a fluid phase (high-vacuum imaging
methods are difficult), makes the small-angle scattering technique, using
light, x-rays, and neutrons, a preferred method of structure determination.
We focus in this talk on neutron scattering, and this method has several
strengths: 1) contrast matching to highlight features is easily achieved
through use of various isotopes, for example $^{1}$H vs $^{2}$H, 2) an
unprecedented range of length scales is accessible (several $\mu $m to nm)
through the combined use of SANS and USANS, and 3) the concentration of
scattering entities is precisely determined because scattering is routinely
measured on an absolute basis. When one considers small-angle scattering
from a dispersion, simple models such as Debye scattering, where the
magnitude of the momentum transfer (q=2$\pi $ Sin($\theta )$/$\lambda )$ is
comparable to the size of the dispersed phases (R*q$\sim $1), is often used
to estimate the size of the dispersed phase. However, this simple approach
fails in many real-world cases where we must deal with, for example, high
concentrations of solids or highly-anisotropic dispersed phases. In this
talk we will illustrate how we have utilized combined SANS / USANS data
along with contrast matching techniques to understand the structure-property
relations governing behavior in several areas of interest, including
self-assembly of polymers in fuel additives, polymer-modified gas-hydrate
slurries, and organoclay dispersion/exfolation as thickening agents.
*I would like to acknowledge the contributions of my ExxonMobil colleagues
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2010.MAR.V5.5