Influence of magnetic field on the orientation of anisotropic magnetic particles at liquid interfaces
Literature Information
Bethany J. Newton, Kenneth A. Brakke, D. Martin A. Buzza
We study theoretically the influence of an external magnetic field on the orientation of an ellipsoidal magnetic particle adsorbed at a liquid interface. Using the finite element program Surface Evolver, we calculate the equilibrium meniscus shape around the ellipsoidal particle and its equilibrium tilt angle with respect to the undeformed interface θt when a magnetic field B is applied perpendicular to the interface. We find that as we increase field strength, θt increases and at a critical magnetic field Bc1 and tilt angle θc1, the particle undergoes a discontinuous transition to the ‘perpendicular’ orientation (θt = 90°). Our results agree qualitatively with the simplified theory of Bresme and Faraudo [F. Bresme and J. Faraudo, J. Phys.: Condens. Matter, 2007, 19, 375110] which assumes that the liquid interface is flat, while they agree quantitatively with recent lattice-Boltzmann simulations of Davies et al. [G. Davies et al., Soft Matter, 2014, 10, 6742] which account for the deformation of the liquid meniscus. We also show for the first time that upon reducing the external magnetic field, at a critical magnetic field Bc2 < Bc1, the particle undergoes a second discontinuous transition from the perpendicular orientation to a finite tilt angle θc2 < θc1. In other words, for micron-sized particles where the thermal energy kBT is negligible compared to the interfacial energy, the tilt angle vs. magnetic field curve exhibits hysteresis behaviour. Due to the higher degree of accuracy of the Surface Evolver method, we are able to analyse the behaviour of the particles near these orientational transitions accurately and study how the critical quantities Bc1, Bc2, θc1 and θc2 vary with particle aspect ratio and contact angle.
Related Literature
Ultrasensitive and reproducible SERS platform of coupled Ag grating with multibranched Au nanoparticles
David Mares, Vitezslav Jerabek, Pavel Ulbrich, Ladislav Lapcak, Vaclav Svorcik
DOI: 10.1039/C7CP01828B
Electrochemical evaluation methods of vanadium flow battery electrodes
Lantao Wu, Jianshe Wang, Yi Shen, Le Liu, Jingyu Xi
DOI: 10.1039/C7CP02581E
Correction: Eu2+–Eu3+ valence transition in double, Eu-, and Na-doped PbSe from transport, magnetic, and electronic structure studies
SunPhil Kim, Yeseul Lee, Bin He, Gloria Lehr, Mercouri G. Kanatzidis, Donald T. Morelli
DOI: 10.1039/C7CP90127E
Vibronic quantized tunneling controlled photoinduced electron transfer in an organic solar cell subjected to an external electric field
Peng Song, Yuanzuo Li, Fengcai Ma
DOI: 10.1039/C7CP02157G
Chiral differentiation of d- and l-alanine by permethylated β-cyclodextrin: IRMPD spectroscopy and DFT methods
Sung-Sik Lee, Soojin Park, Jae-ung Lee, Jun-Hyeok Kim, Dongkyung Yoon, Sungyul Lee, Han Bin Oh
DOI: 10.1039/C7CP01085K
Molecular dynamic heterogeneity in relation to free volume and relaxation dynamics in organic glass-formers: oligomeric cis-1,4-poly(isoprene)
H. Švajdlenková, Z. Nógellová, J. Bartoš
DOI: 10.1039/C7CP00446J
Does Z′ equal 1 or 2? Enhanced powder NMR crystallography verification of a disordered room temperature crystal structure of a p38 inhibitor for chronic obstructive pulmonary disease
Cory M. Widdifield, Sten O. Nilsson Lill, Anders Broo, Maria Lindkvist, Anna Pettersen, Anna Svensk Ankarberg, Peter Aldred, Staffan Schantz, Lyndon Emsley
DOI: 10.1039/C7CP02349A
Elastic properties and short-range structural order in mixed network former glasses
Weimin Wang, Randilynn Christensen, Brittany Curtis, David Hynek, Sydney Keizer, James Wang, Steve Feller, Steve W. Martin, John Kieffer
DOI: 10.1039/C6CP08939A
On the underestimated impact of the gelation temperature on macro- and mesoporosity in monolithic silica
Ulrich Tallarek
DOI: 10.1039/C7CP01846K
Interface passivation and electron transport improvement of polymer solar cells through embedding a polyfluorene layer
Shujun Li, Zhiqi Li, Chunyu Liu, Xinyuan Zhang, Zhihui Zhang, Wenbin Guo, Liang Shen, Shengping Ruan, Liu Zhang
DOI: 10.1039/C7CP01326D
You might also like
What are the main uses of 1-(3-Aminophenyl)-3-[(3R)-1-(3,3-dimethyl-2-oxobutyl)-2-oxo-5-(2-pyridinyl)-2,3-dihydro-1H-1,4-benzodiazepin-3-yl]urea (CAS: 155412-88-7)?
This compound is mainly used as an intermediate in the synthesis of antipsychoti...
How should waste containing 1-(D-Ribofuranosyl)-1,4-dihydro-3-pyridinecarboxamide (CAS: 19132-12-8) be handled?
Waste containing 1-(D-Ribofuranosyl)-1,4-dihydro-3-pyridinecarboxamide (CAS: 191...
What regulatory guidelines apply to 2-Methyl-2-propanyl 3-bromo-3-(hydroxymethyl)-1-azetidinecarboxylate (CAS: 2007919-81-3)?
2-Methyl-2-propanyl 3-bromo-3-(hydroxymethyl)-1-azetidinecarboxylate (CAS: 20079...
What is N-(4-Chloro-2-pyridinyl)acetamide (CAS: 245056-66-0)?
N-(4-Chloro-2-pyridinyl)acetamide (CAS: 245056-66-0) is a chemical compound with...
What is 5-Chloro-2-hydroxybenzoic acid (CAS: 321-14-2)?
5-Chloro-2-hydroxybenzoic acid, also known as 5-chlorosalicylic acid, is an arom...
What precautions should be taken when handling 1,1-Dichloro-1-fluoroethane (CAS: 1717-00-6)?
When handling 1,1-Dichloro-1-fluoroethane (CAS: 1717-00-6), it is important to u...
What are the physical and chemical properties of Fmoc-(2S,3R)-3-phenylpyrrolidine-2-carboxylic acid (CAS: 281655-32-1)?
Fmoc-(2S,3R)-3-phenylpyrrolidine-2-carboxylic acid is a white crystalline solid ...
What are the main uses of 4-Amino-5-bromo-2-pyridinecarboxylic acid (CAS: 1363381-01-4)?
4-Amino-5-bromo-2-pyridinecarboxylic acid is primarily used as a precursor in th...
What precautions should be taken when handling (S)-tert-butyl 2-((2-(4-bromophenyl)-2-oxoethyl)carbamoyl)pyrrolidine-1-carboxylate (CAS: 1007881-98-2)?
Handling this compound should be done with personal protective equipment (PPE) i...
What precautions should be taken when handling 8-bromo-2,2-dimethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one (CAS: 688363-73-7)?
When handling 8-bromo-2,2-dimethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one, use prop...
Source Journal
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.











![Methyl 4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)bicyclo[2.2.2]octane-1-carboxylate structure Methyl 4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)bicyclo[2.2.2]octane-1-carboxylate structure](https://static.chemtradehub.com/structs/943/943845-74-7-b7e5.webp)


