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George Hirasaki

George Hirasaki

· A.J. Hartsook Professor Emeritus, Chemical and Biomolecular Engineering (NAE) Research ProfessorVerified

Rice University · Chemical and Biomolecular Engineering

Active 1968–2024

h-index73
Citations17.5k
Papers28936 last 5y
Funding
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Research topics

  • Organic chemistry
  • Chemistry
  • Chemical physics
  • Materials science
  • Physics
  • Thermodynamics
  • Chemical engineering
  • Nuclear magnetic resonance
  • Inorganic chemistry
  • Chromatography
  • Computational chemistry

Selected publications

  • Elucidating the <sup>1</sup>H NMR Relaxation Mechanism in Polydisperse Polymers and Bitumen Using Measurements, MD Simulations, and Models

    The Journal of Physical Chemistry B · 2020 · 34 citations

    • Materials science
    • Nuclear magnetic resonance
    • Thermodynamics

    dispersion at high viscosities agrees with previously reported MD simulations of heptane confined in a polymer matrix, which suggests a common NMR relaxation mechanism between viscous polydisperse fluids and fluids under nanoconfinement, without the need to invoke paramagnetism.

  • Critical Role of Confinement in the NMR Surface Relaxation and Diffusion of <i>n</i>-Heptane in a Polymer Matrix Revealed by MD Simulations

    The Journal of Physical Chemistry B · 2020 · 31 citations

    • Chemistry
    • Chemical physics
    • Materials science

    H dipole-dipole interactions enhanced by organic nanopore confinement dominate the NMR response in saturated organic-rich shales.

  • Role of Wettability on the Adsorption of an Anionic Surfactant on Sandstone Cores

    Langmuir · 2020 · 55 citations

    • Chemistry
    • Chemical engineering
    • Inorganic chemistry

    alpha olefin sulfonate on Berea sandstone cores with different surface wettability and redox states under high temperature that represents reservoir conditions. Surfactant adsorption levels are determined by analyzing the effluent history data with a dynamic adsorption model assuming Langmuir isotherm. A variety of analyses, including surface chemistry, ionic composition, and chromatography, is performed. It is found that the surfactant breakthrough in the neutral-wet core is delayed more compared to that in the water-wet core because the deposited crude oil components on the rock surface increase the surfactant adsorption via hydrophobic interactions. As the surfactant adsorption is satisfied, the crude oil components are solubilized by surfactant micelles and some of the adsorbed surfactants are released from the rock surface. The released surfactant dissolves in the flowing surfactant solution, thereby resulting in an overshoot of the produced surfactant concentration with respect to the injection value. Furthermore, under water-wet conditions, changing the surface redox potential from an oxidized to a reduced state decreases the surfactant adsorption level by 40%. We find that the decrease in surfactant adsorption is caused not only by removing the iron oxide but also by changing the calcium concentration after the core restoration process (calcite dissolution and ion exchange as a result of using EDTA). Findings from this study suggest that laboratory surfactant adsorption tests need to be conducted by considering the wettability and redox state of the rock surface while recognizing how core restoration methods could significantly alter the ionic composition during surfactant flooding.

Frequent coauthors

Education

  • PhD, Chemical & Biomolecular Engineering

    Rice University

    1967
  • B.S., Chemical Engineering

    Lamar University

    1963

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