Brian Vincent
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Brian Vincent has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Antonio Fernandez-Barbero
NonLinear and Materials Physics Group (UAL), Materials for Solar Thermal and Photovoltaic Energy Group, CIESOL (UAL‐Ciemat), Department of Chemistry and Physics University of Almeria Almeria Spain
1 shared publication Darby Kozak
School of Chemistry, University of Bristol , Bristol, United Kingdom
1 shared publicationDavid Moreton
Lubrizol International Laboratories , Derby, United Kingdom
1 shared publicationMark Davies
Lubrizol International Laboratories , Derby, United Kingdom
1 shared publicationN. G. Wright
University of Bristol
1 shared publicationN. J. Marston
University of Bristol
1 shared publication
Latest Publications
- 1 September 2019
- Published by Elsevier in Advances in Colloid and Interface Science
- Vol. 271, 101981
Hans Lyklema's promotion of colloid and Interface science on the international stage
- 1 September 2019
- Published by Elsevier in Advances in Colloid and Interface Science
- Vol. 271, 101981
Hans Lyklema's promotion of colloid and Interface science on the international stage
- 1 January 2012
- Published by Elsevier in Advances in Colloid and Interface Science
- Vol. 170 (1-2) , 56-67
Early (pre-DLVO) studies of particle aggregation
- 1 January 2012
- Published by Elsevier in Advances in Colloid and Interface Science
- Vol. 170 (1-2) , 56-67
Early (pre-DLVO) studies of particle aggregation
- 27 May 2009
- Published by Taylor & Francis in Journal of Dispersion Science and Technology
- Vol. 30 (6) , 782-788
The Adsorption of Nonionic Surfactants onto Stainless Steel Surfaces from Iso-Octane
The synthesis of nine, nonionic, fuel-soluble poly(isobutylene)-based surfactants, and an assessment of their ability to remove and prevent carbonaceous deposit build up on light-duty vehicle engine valves, is described. Surfactants with varying surfactant head group polarity and structure, and tail length, were assessed for their potential fuel surfactant efficacy by establishing their adsorption kinetics and adsorption isotherms, from iso-octane, onto stainless steel surfaces, using both solution depletion and ellipsometry measurements. Increasing head group polarity from a simple phenol group, by the inclusion of an amine group, increased the adsorption affinity and the maximum adsorbed amount. Inclusion of additional amine groups also increased them maximum adsorbed amount, albeit only marginally. Replacing N-Me groups by N-H groups also increased the adsorbed amounts. Surfactant adsorption was found to be independent of tail length and the maximum adsorbed amount corresponded more-or-less to the surface concentration of strong acid groups on the steel surface, as determined by a Boehm titration. Additionally, all the surfactants studied appeared to adsorb onto the steel surface “irreversibly.”
- 27 May 2009
- Published by Taylor & Francis in Journal of Dispersion Science and Technology
- Vol. 30 (6) , 782-788
The Adsorption of Nonionic Surfactants onto Stainless Steel Surfaces from Iso-Octane
The synthesis of nine, nonionic, fuel-soluble poly(isobutylene)-based surfactants, and an assessment of their ability to remove and prevent carbonaceous deposit build up on light-duty vehicle engine valves, is described. Surfactants with varying surfactant head group polarity and structure, and tail length, were assessed for their potential fuel surfactant efficacy by establishing their adsorption kinetics and adsorption isotherms, from iso-octane, onto stainless steel surfaces, using both solution depletion and ellipsometry measurements. Increasing head group polarity from a simple phenol group, by the inclusion of an amine group, increased the adsorption affinity and the maximum adsorbed amount. Inclusion of additional amine groups also increased them maximum adsorbed amount, albeit only marginally. Replacing N-Me groups by N-H groups also increased the adsorbed amounts. Surfactant adsorption was found to be independent of tail length and the maximum adsorbed amount corresponded more-or-less to the surface concentration of strong acid groups on the steel surface, as determined by a Boehm titration. Additionally, all the surfactants studied appeared to adsorb onto the steel surface “irreversibly.”
- 2 February 2008
- Published by Springer Nature
- p. 278-282
The synthesis of spherical rutile titanium dioxide particles and their interaction with polystyrene latex particles of opposite charge
- 2 February 2008
- Published by Springer Nature
- p. 278-282
The synthesis of spherical rutile titanium dioxide particles and their interaction with polystyrene latex particles of opposite charge
- 1 November 2003
- Published by Elsevier in Colloids and Surfaces A: Physicochemical and Engineering Aspects
- Vol. 228 (1-3) , 181-187
Particle formation and gelling behaviour of anionic oligoesters in aqueous solution
- 1 November 2003
- Published by Elsevier in Colloids and Surfaces A: Physicochemical and Engineering Aspects
- Vol. 228 (1-3) , 181-187
Particle formation and gelling behaviour of anionic oligoesters in aqueous solution
- 22 December 2000
- Published by American Physical Society (APS) in Physical Review E
- Vol. 63 (1) , 011509
Charge heteroaggregation between hard and soft particles
In this paper, the heteroaggregation of opposite sign hard and soft colloidal particles has been studied by static and dynamic light scattering. The structure of the aggregates, as well as the aggregation kinetics, have been investigated. At low electrolyte concentration, where both long-range electrostatic repulsive and attractive forces are present, the aggregates were found to be more open than expected for diffusion-limited cluster aggregation (DLCA). However, the aggregate size time evolution is characteristic of diffusion-controlled processes. At high electrolyte concentration, where DLCA would be expected, very compacted clusters were found, as well as very rapid aggregation, leading to high polydispersity. These latter findings are interpreted in terms of the differences in the homoaggregation speeds for the hard and soft particles.
- 22 December 2000
- Published by American Physical Society (APS) in Physical Review E
- Vol. 63 (1) , 011509
Charge heteroaggregation between hard and soft particles
In this paper, the heteroaggregation of opposite sign hard and soft colloidal particles has been studied by static and dynamic light scattering. The structure of the aggregates, as well as the aggregation kinetics, have been investigated. At low electrolyte concentration, where both long-range electrostatic repulsive and attractive forces are present, the aggregates were found to be more open than expected for diffusion-limited cluster aggregation (DLCA). However, the aggregate size time evolution is characteristic of diffusion-controlled processes. At high electrolyte concentration, where DLCA would be expected, very compacted clusters were found, as well as very rapid aggregation, leading to high polydispersity. These latter findings are interpreted in terms of the differences in the homoaggregation speeds for the hard and soft particles.