
NSF Org: |
DMS Division Of Mathematical Sciences |
Recipient: |
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Initial Amendment Date: | September 15, 2016 |
Latest Amendment Date: | September 15, 2016 |
Award Number: | 1620152 |
Award Instrument: | Standard Grant |
Program Manager: |
Leland Jameson
DMS Division Of Mathematical Sciences MPS Directorate for Mathematical and Physical Sciences |
Start Date: | September 15, 2016 |
End Date: | August 31, 2021 (Estimated) |
Total Intended Award Amount: | $98,248.00 |
Total Awarded Amount to Date: | $98,248.00 |
Funds Obligated to Date: |
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History of Investigator: |
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Recipient Sponsored Research Office: |
1 NORMAL AVE MONTCLAIR NJ US 07043-1624 (973)655-6923 |
Sponsor Congressional District: |
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Primary Place of Performance: |
1 Normal Avenue Montclair NJ US 07043-1624 |
Primary Place of
Performance Congressional District: |
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Unique Entity Identifier (UEI): |
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Parent UEI: |
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NSF Program(s): | COMPUTATIONAL MATHEMATICS |
Primary Program Source: |
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Program Reference Code(s): |
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Program Element Code(s): |
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Award Agency Code: | 4900 |
Fund Agency Code: | 4900 |
Assistance Listing Number(s): | 47.049 |
ABSTRACT
Advances in the synthesis of Ferrofluids (engineered fluids that respond to magnetic fields and have a number of well-established industrial applications) have increased the scope of potential applications of these fluids to new areas. Emerging applications of ferrofluids include: magnetic targeting of drugs, cell sorting in biomedical systems and magnetically driven contaminant removal. In each of these applications the use of ferrofluids enables new techniques that depend on the use of magnetic fields for 'remote control' of the ferrofluid. However, the realization of such technologies is hampered by complexities in the simulation of these systems for further development and design. The proposed research program includes the development of effective, robust computational tools that will enable such simulations. In particular, the computing codes will include the particular magnetic physics of ferrofluids as well as the forces resulting from the magnetic fields, which serve as the means of control in these applications. The development of these effective simulation tools will support and accelerate innovation in these emerging technologies. Moreover, the proposed program of code development, simulations and integrated physical experiments will serve as a proof-of-concept for the inclusion of realistic multiphysics fluid simulations for complex scientific and engineering applications. The proposed research program will involve undergraduate and masters-degree students in leading-edge research, including students who are members of groups under-represented in STEM disciplines such as women and first-generation college students.
In magnetic drug targeting, a ferrofluid whose constituent nanoparticles have been functionalized to carry theraputic drugs is directed to a tumor or other localized site (e.g., in the eye); sorting of(nonmagnetic) biological cells by immersion in a ferrofluid so that the force of an applied magnetic field depends on cell size; purification of a polluted fluid by adsorption of contaminants to magnetic nanoparticles, which are then separated from the fluid by magnetic forces. However, advances in these applications are stymied by the complex, multi-scale and multi-physics nature of the fluid-dynamical systems in which they occur. In particular, because contemporary fluid-dynamics codes are not designed to incorporate the additional physics of magnetic-fluid systems, effective simulation with these codes is difficult. The proposal describes a plan to develop and test a new parallel, multi-phase code for fully three-dimensional flows. This project will lead to a flexible and efficient, multi-phase magnetic-fluid simulation code that is fully three-dimensional and parallelized for high-performance computing. Hence, the code will enable realistic simulations relevant to the significant applications addressed. Specifically, in order to address the above-noted applications, the code will model and simulate flows with dynamic interfaces between the ferrofluid and other fluids. Moreover, the code will implement models of viscosity effects (magnetoviscosity) as well as driving forces that result from applied magnetic fields (magnetophoresis) in a flexible manner that simplifies adjustment and update of the models.
PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH
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PROJECT OUTCOMES REPORT
Disclaimer
This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.
The central focus of this collaborative project was the development, implementation, and testing of algorithms for simulation of magnetically driven multiphase flows with magnetizable liquids. The resulting code is the first platform for general simulation of fully three-dimensional multiphase flows with magnetic effects, and was developed within the framework of the open-access Parallel Robust Interface Simulator (PARIS) architecture.
Demonstration simulations of the implementation included the mutual repulsion of droplets magnetized by an external field, with the motion of each droplet driven by spatial variation, induced by the other droplet, of the overall magnetic field. This phenomenon cannot be reduced to a lower dimensional computation (e.g., by symmetry) and therefore required a fully three-dimensional simulation platform.
The generality in the implementation of the magnetic-field and magnetic-force computations in the code allows the simulation of a wide range of configurations and fluid properties. Moreover, implementation of magnetic effects as an extension of the PARIS architecture serves as a proof-of-concept for inclusion of further multiphysics phenomena in simulations of interfacial flows. These aspects enable potential applications to problems in many fields, including microfluidics and biomedical engineering.
To investigate the fidelity of simulations, the project also included: (i) development of a laboratory apparatus that allows quantitative measurement of the dynamics of magnetically captured magnetizable fluid bolus immersed in a non-magnetic fluid with an externally driven flow; (ii) theoretical investigation of the shape and interactions among droplets magnetized by an external field. Furthermore, an apparatus was developed (with standard, low-cost components) to detect, track and control the motion of small regions of magnetic fluid in an environment resembling biological tissue or blood vessel, as a test model of magnetically driven drug targeting.
All of the research activity performed in this project involved undergraduate and masters-degree students as key participants, including presentations at international conferences, as well as the co-authoring of articles in peer-reviewed journals. In addition, two applied mathematics masters-degree degree capstone projects were completed at Montclair State University under this project. Collaboration included support and advising for additional student research participants at the Cooper Union.
Last Modified: 07/11/2022
Modified by: A. David Trubatch
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