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Johann Fischbacher

Publications and source records attributed to Johann Fischbacher.

22 records · Page 2Linked to original sources

Thermal activation in permanent magnets

The coercive field of permanent magnets decays with temperature. At non-zero temperature the system can overcome a finite energy barrier through thermal fluctuations. Using finite element micromagnetic simulations, we quantify this effect, which reduces coercivity in addition to the decrease of the coercive field associated with the temperature dependence of the anisotropy field, and validate the method through comparison with existing experimental data.

cond-mat.mtrl-sci↗

Micromagnetics of shape anisotropy based permanent magnets

In the search for rare-earth free permanent magnets, various ideas related to shape anisotropy are being pursued. In this work we assess the limits of shape contributions to the reversal stability using micromagnetic simulations. In a first series of tests we altered the aspect ratio of single phase prolate spheroids from 1 to 16. Starting with a sphere of radius $4.3$ times the exchange length $ L_{\mathrm{ex}}$ we kept the total magnetic volume constant as the aspect ratio was modified. For a ferromagnet with zero magnetocrystalline anisotropy the maximum coercive field reached up to $0.5$ times the magnetization $M_{\mathrm{s}}$. Therefore, in materials with moderate uniaxial magnetocrystalline anisotropy, the addition of shape anisotropy could even double the coercive field. Interestingly due to non-uniform magnetization reversal there is no significant increase of the coercive field for an aspect ratio greater than 5. A similar limit of the maximum aspect ratio was observed in cylinders. The coercive field depends on the wire diameter. By decreasing the wire diameter from $8.7 L_{\mathrm{ex}}$ to $2.2 L_{\mathrm{ex}}$ the coercive field increased by 40%. In the cylinders nucleation of a reversed domain starts at the corners at the end. Smoothing the edges can improve the coercive field by about 10%. In further simulations we compacted soft magnetic cylinders into a bulk-like arrangement. Misalignment and magnetostatic interactions cause a spread of $0.1 M_{\mathrm{s}}$ in the switching fields of the rods. Comparing the volume averaged hysteresis loops computed for isolated rods and the hysteresis loop computed for interacting rods, we conclude that magnetostatic interactions reduce the coercive field by up to 20%.

cond-mat.mtrl-sci↗

Guided self-assembly of magnetic beads for biomedical applications

Micromagnetic beads are widely used in biomedical applications for cell separation, drug delivery, and hypothermia cancer treatment. Here we propose to use self-organized magnetic bead structures which accumulate on fixed magnetic seeding points to isolate circulating tumor cells. The analysis of circulating tumor cells is an emerging tool for cancer biology research and clinical cancer management including the detection, diagnosis and monitoring of cancer. Microfluidic chips for isolating circulating tumor cells use either affinity, size or density capturing methods. We combine multiphysics simulation techniques to understand the microscopic behavior of magnetic beads interacting with Nickel accumulation points used in lab-on-chip technologies. Our proposed chip technology offers the possibility to combine affinity and size capturing with special antibody-coated bead arrangements using a magnetic gradient field created by Neodymium Iron Boron permanent magnets. The multiscale simulation environment combines magnetic field computation, fluid dynamics and discrete particle dynamics.

physics.bio-ph↗

Simulation of magnetic active polymers for versatile microfluidic devices

We propose to use a compound of magnetic nanoparticles (20-100 nm) embedded in a flexible polymer (Polydimethylsiloxane PDMS) to filter circulating tumor cells (CTCs). The analysis of CTCs is an emerging tool for cancer biology research and clinical cancer management including the detection, diagnosis and monitoring of cancer. The combination of experiments and simulations lead to a versatile microfluidic lab-on-chip device. Simulations are essential to understand the influence of the embedded nanoparticles in the elastic PDMS when applying a magnetic gradient field. It combines finite element calculations of the polymer, magnetic simulations of the embedded nanoparticles and the fluid dynamic calculations of blood plasma and blood cells. With the use of magnetic active polymers a wide range of tunable microfluidic structures can be created. The method can help to increase the yield of needed isolated CTCs.

physics.bio-ph↗