We utilize an effective field theory approach to calculate Casimir interactions between objects bound to thermally fluctuating fluid surfaces or interfaces. This approach circumvents the complicated constraints imposed by such objects on the functional integration measure by reverting to a point particle representation. To capture the finite size effects, we perturb the Hamiltonian by ∆H that encapsulate the particles' response to external fields. ∆H is systematically expanded in a series of terms, each of which scales homogeneously in the two power counting parameters: λ ≡ R/r , the ratio of the typical object size (R) to the typical distance between them (r), and δ ≡ kBT /k, where k is the modulus characterizing the surface energy. The coefficients of the terms in ∆H correspond to generalized polarizabilities and thus the formalism applies to rigid as well as deformable objects. Singularities induced by the point particle description can be dealt with using standard renormalization techniques. We first illustrate and verify our approach by re-deriving known pair forces between circular objects bound to films or membranes. To demonstrate its efficiency and versatility, we then derive a number of new results: The triplet interactions present in these systems, a higher order correction to the film interaction, and general scaling laws for the leading order interaction valid for objects of arbitrary shape and internal flexibility.
We study the influence of diffusion on NMR experiments when the molecules undergo random motion under the influence of a force field, and place special emphasis on parabolic (Hookean) potentials. To this end, the problem is studied using path integral methods. Explicit relationships are derived for commonly employed gradient waveforms involving pulsed and oscillating gradients. The Bloch-Torrey equation, describing the temporal evolution of magnetization, is modified by incorporating potentials. A general solution to this equation is obtained for the case of parabolic potential by adopting the multiple correlation function (MCF) formalism, which has been used in the past to quantify the effects of restricted diffusion. Both analytical and MCF results were found to be in agreement with random walk simulations. A multi-dimensional formulation of the problem is introduced that leads to a new characterization of diffusion anisotropy. Unlike for the case of traditional methods that employ a diffusion tensor, anisotropy originates from the tensorial force constant, and bulk diffusivity is retained in the formulation. Our findings suggest that some features of the NMR signal that have traditionally been attributed to restricted diffusion are accommodated by the Hookean model. Under certain conditions, the formalism can be envisioned to provide a viable approximation to the mathematically more challenging restricted diffusion problems. * Electronic address: evren.ozarslan@boun.edu.tr
An approach based on effective field theory (EFT) is discussed and applied to the problem of surface-mediated interactions between rigid inclusions of circular footprint on a membrane. Instead of explicitly constraining the surface fluctuations in accord with the boundary conditions around the inclusions, the EFT formalism rewrites the theory; the Hamiltonian of a freely fluctuating surface is augmented by pointwise localized terms that capture the same constraints. This allows one to compute the interaction free energy as an asymptotic expansion in inverse separations in a systematic, efficient, and transparent way. Both entropic (fluctuation-induced, Casimir-like) and curvature-elastic (ground-state) forces are considered. Our findings include higher-order corrections to known asymptotic results, on both the pair and the multibody levels. We also show that the few previous attempts in the literature at predicting subleading orders missed some terms due to an uncontrolled point-particle approximation.
Diffusion-attenuated MR signal for heterogeneous media has been represented as a sum of signals from anisotropic Gaussian sub-domains to the extent that this approximation is permissible. Any effect of macroscopic (global or ensemble) anisotropy in the signal can be removed by averaging the signal values obtained by differently oriented experimental schemes. The resulting average signal is identical to what one would get if the micro-domains are isotropically (e.g., randomly) distributed with respect to orientation, which is the case for “powdered” specimens. We provide exact expressions for the orientationally-averaged signal obtained via general gradient waveforms when the microdomains are characterized by a general diffusion tensor possibly featuring three distinct eigenvalues. This extends earlier results which covered only axisymmetric diffusion as well as measurement tensors. Our results are expected to be useful in not only multidimensional diffusion MR but also solid-state NMR spectroscopy due to the mathematical similarities in the two fields.
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