PubMed Health⌕ Search

Biomedical subjects

AR Rennie

Publications and source records attributed to AR Rennie.

5 recordsLinked to original sources

Monodisperse colloidal plates under shear

The structure of a dispersion of monodispersed, plate-shaped colloidal particles has been investigated under shear. The dispersion displays a columnar phase when at rest, and if subjected to shear at low rates (0.1-1 s(-1)), this structure aligns with the axis of the columns in the flow direction. At low shear rates, the plates within these columns are tilted, with their normals in the compressional quadrant, at 20 degrees to the flow direction in the flow-gradient plane. At high shear rates ( approximately 100 s(-1)), the dispersion forms a different structure that consists of layers of particles with their plate normals in the gradient direction. The transition between these two shear-induced "phases" is described. Evidence is presented that suggests that at intermediate shear rates there is coexistence between the two phases, implying that there is a shear-induced "phase separation." As the shear rate is further increased evidence for shear-induced disorder is found. All the shear-induced structures that have been observed relax back to the equilibrium columnar phase over a period of a few hours. At rest after shear at low rates (0.1-1 s(-1)), the amount of orientational order present in the aligned columnar phase increases, while there is no measurable positional rearrangement. After shear at high rates (67-1000 s(-1)), the layer phase relaxes into a columnar phase. The structure changes via an intermediate state consisting of planes of particles normal to the vorticity direction. The positional rearrangement occurs at the expense of the orientational order, which increases again after the positional rearrangement is complete. The final orientation of the columnar phase is such that the direction of alignment of the plates does not change upon relaxation.

Journal Article↗

Fabricating colloidal particles with photolithography and their interactions at an air-water interface

A technique for fabricating nonspherical colloidal particles using photolithography has been developed. The particles are plate shaped and their profile within the plane of the plate is defined by a lithography mask and so can be any form desired. The thickness of the particles can also be controlled by varying the amount of material in the particle, and also by using the stresses induced during the evaporation of materials to distort the particles out of the plane. The particle-particle interactions can be tailored and made anisotropic by coating different faces of the particles with different chemicals or by making them of different materials. This technique is used to produce curved disks that are hydrophobic on their convex face and hydrophilic on their concave face. These particles are studied at an air-water interface, where the majority lie with their hydrophobic face uppermost. The curvature of the particles distorts the water surface in a manner that can be described by a series expansion. The symmetry of this function is used to explain the interactions of the particles and the resulting ordered flocculated structures observed. Such anisotropic forces in two dimensions have not been studied previously on a colloidal length scale to our knowledge and extend the field of control of particles at interfaces.

Journal Article↗

The Denaturation of Lysozyme Layers Adsorbed at the Hydrophobic Solid/Liquid Surface Studied by Neutron Reflection.

We have studied the adsorption of lysozyme layers at a hydrophobic silicon water interface using specular neutron reflection. The hydrophobic surface was obtained by self-assembly of a densely packed monolayer of octadecyltrichlorosilane (OTS) onto the natural silica layer on the smooth surface of a (111) silicon block. The effect of pH on the adsorbed lysozyme layer was examined at a constant lysozyme concentration of 0.03 g dm-3 and at a constant ionic strength of 0.02 M. Reflectivity profiles at different pH show that adsorption is irreversible with respect to pH, the composition and structure of the final layer being dependent on the route by which the pH was achieved. The adsorbed protein layer was found to divide into approximately two regions, a densely packed thin layer next to the OTS surface and a diffuse thicker layer extending into the bulk solution. None of the dimensions of this structure corresponds to those of the globular protein in solution, suggesting that, unlike its adsorption at the hydrophilic silica/water interface, lysozyme is denatured at the OTS/water surface. The irreversible adsorption is explained by the combined interaction of the hydrophobic attraction of the hydrophobic fragments in lysozyme to the OTS surface and electrostatic repulsion within the adsorbed layer. The hydrophobic surface induces the exposure of hydrophobic fragments from the lysozyme assembly. The thickness of the dense layer suggests that the denatured protein adsorbs in the form of peptide chains with the hydrophobic amino acid side chains attached to the OTS surface with the hydrophilic side chains extending into the bulk solution. Since lysozyme is more stable at pH 7 than at pH 4, the difference in initial adsorption is dominated by the greater relative stability of lysozyme to denaturation at the higher pH. A change of pH from 7 to 4 reduces the stability of the protein to unfolding and results in more adsorption than when the pH is changed in the opposite direction. Solution pH also affects the net charges within the hydrophilic tail region and the structural distribution of the tail region was found to vary with pH. Copyright 1998 Academic Press.

Journal Article↗