The spin-spin relaxation in connective tissues is simulated using a model in which a connective tissue is represented by a set of nanocavities containing HO-DO liquid. Collagen fibrils in connective tissues form ordered hierarchical long structures of hydrated nano-cavities with characteristic diameter from 1 nm to several tens of nanometers and length of about 100 nm. We consider influence of the restricted Brownian motion of molecules inside a nano-cavity on spin-spin relaxation.
View Article and Find Full Text PDFThis study investigates the fibril nanostructure of fresh celery samples by modeling the anisotropic behavior of the transverse relaxation time (T) in nuclear magnetic resonance (NMR). Experimental results are interpreted within the framework of a previously developed theory, which was successfully used to model the nanostructures of several biological tissues as a set of water filled nanocavities, hence explaining the anisotropy the T relaxation time in vivo. An important feature of this theory is to determine the degree of orientational ordering of the nanocavities, their characteristic volume, and their average direction with respect to the macroscopic sample.
View Article and Find Full Text PDFWe studied the anisotropy of H NMR spin-lattice and spin-spin relaxations in a fresh celery stem experimentally and modeled the sample theoretically as the water-containing nano- and micro-cavities. The angular dependence of the spin-lattice and the spin-spin relaxation times was obtained, which clearly shows the presence of water-filled nano- and micro-cavities in the celery stem, which have elongated shapes and are related to non-spherical vascular cells in the stem. To explain the experimental data, we applied the relaxation theory developed by us and used previously to interpret similar effects in liquids in nanocavities located in biological tissues such as cartilages and tendons.
View Article and Find Full Text PDFWe analyze the application of the spin locking method to study the spin dynamics and spin-lattice relaxation of nuclear spins-1/2 in liquids or gases enclosed in a nano-cavity. Two cases are considered: when the amplitude of the radio-frequency field is much greater than the local field acting the nucleus and when the amplitude of the radio-frequency field is comparable or even less than the local field. In these cases, temperatures of two spin reservoirs, the Zeeman and dipole ones, change in different ways: in the first case, temperatures of the Zeeman and dipolar reservoirs reach the common value relatively quickly, and then turn to the lattice temperature; in the second case, at the beginning of the process, these temperatures are equal, and then turn to the lattice temperature with different relaxation times.
View Article and Find Full Text PDFWe consider the spin lattice relaxation in bulk liquid and liquid entrapped in a nanocavity. The kinetic equation which describes the spin lattice relaxation is obtained by using the theory of the nonequilibrium state operator. A solution of the kinetic equation gives the quadrature expression for the relaxation time, T.
View Article and Find Full Text PDFStudy of the spin-lattice relaxation in the spin-locking state offers important information about atomic and molecular motions, which cannot be obtained by spin lattice relaxation in strong external magnetic fields. The application of this technique for the investigation of the spin-lattice relaxation in biological samples with fibril structures reveals an anisotropy effect for the relaxation time under spin locking, T. To explain the anisotropy of the spin-lattice relaxation under spin-locking in connective tissue a model which represents a tissue by a set of nanocavities containing water is used.
View Article and Find Full Text PDFTransverse spin-spin relaxation of liquids entrapped in nanocavities with different orientational order is theoretically investigated. Based on the bivariate normal distribution of nanocavities directions, we have calculated the anisotropy of the transverse relaxation time for biological systems, such as collagenous tissues, articular cartilage, and tendon. In the framework of the considered model, the dipole-dipole interaction is determined by a single coupling constant.
View Article and Find Full Text PDFSpin-spin and spin-lattice relaxations in liquid or gas entrapped in nanosized ellipsoidal cavities with different orientation ordering are theoretically investigated. The model is flexible in order to be applied to explain experimental results in cavities with various forms, from very prolate up to oblate ones, and different degree of ordering of nanocavities. In the framework of the considered model, the dipole-dipole interaction is determined by a single coupling constant, which depends on the form, size, and orientation of the cavity and number of nuclear spins in the cavity.
View Article and Find Full Text PDFWe study the spin-lattice relaxation of the nuclear spins in a liquid or a gas entrapped in nanosized ellipsoidal cavities with paramagnetic impurities. Two cases are considered where the major axes of cavities are in orientational order and isotropically disordered. The evolution equation and analytical expression for spin lattice relaxation time are obtained which give the dependence of the relaxation time on the structural parameters of a nanocavity and the characteristics of a gas or a liquid confined in nanocavities.
View Article and Find Full Text PDFAmplification of a single-spin state using nuclear magnetic resonance (NMR) techniques in a rotating frame is considered. The main aim is to investigate the efficiency of various schemes for quantum detection. Results of numerical simulation of the time dependence of individual and total nuclear polarizations for 1D, 2D, and 3D configurations of the spin systems are presented.
View Article and Find Full Text PDFPhys Rev E Stat Nonlin Soft Matter Phys
August 2003
Two competing irreversible reactions with initially separated components and with essentially different reaction constants are theoretically studied in the asymptotic time region. The description of the two simultaneous reactions is reduced to the consideration of two reactions separated in space. It is shown that the reaction rate profile can have two maxima and their ratio is independent of time.
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