262 research outputs found
A temperature and magnetic field dependence Mössbauer study of ɛ-Fe2O3
ɛ-Fe2O3 was synthesized as nanoparticles by a pre-vacuum heat treatment of yttrium iron garnet (Y3Fe5O12) in a silica matrix at 300-C followed by sintering in air at 1,000-C for up to 10 h. It displays complex magnetic properties that are characterized by two transitions, one at 480 K from a paramagnet (P) to canted antiferromagnet (CAF1) and the second at ca. 120 K from the canted antiferromagnet (CAF1) to another canted antiferromagnet (CAF2). CAF2 has a smaller resultant magnetic moment (i.e. smaller canting angle) than CAF1. Analysis of the zero-field Mossbauer spectra at different temperatures shows an associated discontinuity of the hyperfine field around 120 K. In an applied field, the different magnetic sublattices were identified and the directions of their moments were assigned. The moments of the two sublattices are antiparallel and collinear at 160 K but are at right angle to each other at 4.2 K
Surface effects in nanoparticles: application to maghemite -Fe_{2}O_{3}
We present a microscopic model for nanoparticles, of the maghemite (% -FeO) type, and perform classical Monte Carlo simulations of
their magnetic properties. On account of M\"{o}ssbauer spectroscopy and
high-field magnetisation results, we consider a particle as composed of a core
and a surface shell of constant thickness. The magnetic state in the particle
is described by the anisotropic classical Dirac-Heisenberg model including
exchange and dipolar interactions and bulk and surface anisotropy. We consider
the case of ellipsoidal (or spherical) particles with free boundaries at the
surface. Using a surface shell of constant thickness ( nm) we vary
the particle size and study the effect of surface magnetic disorder on the
thermal and spatial behaviors of the net magnetisation of the particle. We
study the shift in the surface ``critical region'' for different
surface-to-core ratios of the exchange coupling constants. It is also shown
that the profile of the local magnetisation exhibits strong temperature
dependence, and that surface anisotropy is reponsible for the non saturation of
the magnetisation at low temperatures.Comment: 15 pages, 7 figures, to appear in Eur. Phys. J.
Finite-size versus Surface effects in nanoparticles
We study the finite-size and surface effects on the thermal and spatial
behaviors of the magnetisation of a small magnetic particle. We consider two
systems: 1) A box-shaped isotropic particle of simple cubic structure with
either periodic or free boundary conditions. This case is treated analytically
using the isotropic model of D-component spin vectors in the limit , including the magnetic field. 2) A more realistic particle (-FeO) of ellipsoidal (or spherical) shape with open boundaries.
The magnetic state in this particle is described by the anisotropic classical
Dirac-Heisenberg model including exchange and dipolar interactions, and bulk
and surface anisotropy. This case is dealt with by the classical Monte Carlo
technique. It is shown that in both systems finite-size effects yield a
positive contribution to the magnetisation while surface effects render a
larger and negative contribution, leading to a net decrease of the
magnetisation of the small particle with respect to the bulk system. In the
system 2) the difference between the two contributions is enhanced by surface
anisotropy. The latter also leads to non saturation of the magnetisation at low
temperatures, showing that the magnetic order in the core of the particle is
perturbed by the magnetic disorder on the surface. This is confirmed by the
profile of the magnetisation.Comment: 6 pages of RevTex including 4 Figures, invited paper to 3rd
EuroConference on Magnetic Properties of Fine Nanoparticles, Barcelona,
October 9
Field dependence of the temperature at the peak of the ZFC magnetization
The effect of an applied magnetic field on the temperature at the maximum of
the ZFC magnetization, , is studied using the recently obtained
analytic results of Coffey et al. (Phys. Rev. Lett. {\bf 80}(1998) 5655) for
the prefactor of the N\'{e}el relaxation time which allow one to precisely
calculate the prefactor in the N\'{e}el-Brown model and thus the blocking
temperature as a function of the coefficients of the Taylor series expansion of
the magnetocrystalline anisotropy. The present calculations indicate that even
a precise determination of the prefactor in the N\'{e}el-Brown theory, which
always predicts a monotonic decrease of the relaxation time with increasing
field, is insufficient to explain the effect of an applied magnetic field on
the temperature at the maximum of the ZFC magnetization. On the other hand, we
find that the non linear field-dependence of the magnetization along with the
magnetocrystalline anisotropy appears to be of crucial importance to the
existence of this maximum.Comment: 14 LaTex209 pages, 6 EPS figures. To appear in J. Phys.: Condensed
Matte
Management of emerging multidrug-resistant tuberculosis in a low-prevalence setting
AbstractMultidrug-resistant (MDR) tuberculosis (TB) is an emerging concern in communities with a low TB prevalence and a high standard of public health. Twenty-three consecutive adult MDR TB patients who were treated at our institution between 2007 and 2013 were reviewed for demographic characteristics and anti-TB treatment management, which included surgical procedures and long-term patient follow-up. This report of our experience emphasizes the need for an individualized approach as MDR TB brings mycobacterial disease management to a higher level of expertise, and for a balance to be found between international current guidelines and patient-tailored treatment strategies
Quantitative imaging of concentrated suspensions under flow
We review recent advances in imaging the flow of concentrated suspensions,
focussing on the use of confocal microscopy to obtain time-resolved information
on the single-particle level in these systems. After motivating the need for
quantitative (confocal) imaging in suspension rheology, we briefly describe the
particles, sample environments, microscopy tools and analysis algorithms needed
to perform this kind of experiments. The second part of the review focusses on
microscopic aspects of the flow of concentrated model hard-sphere-like
suspensions, and the relation to non-linear rheological phenomena such as
yielding, shear localization, wall slip and shear-induced ordering. Both
Brownian and non-Brownian systems will be described. We show how quantitative
imaging can improve our understanding of the connection between microscopic
dynamics and bulk flow.Comment: Review on imaging hard-sphere suspensions, incl summary of
methodology. Submitted for special volume 'High Solid Dispersions' ed. M.
Cloitre, Vol. xx of 'Advances and Polymer Science' (Springer, Berlin, 2009);
22 pages, 16 fig
Impaired flow-induced arterial remodeling in DOCA-salt hypertensive rats
Arteries from young healthy animals respond to chronic changes in blood flow and blood pressure by structural remodeling. We tested whether the ability to respond to decreased (-90%) or increased (+100%) blood flow is impaired during the development of deoxycorticosterone acetate (DOCA)-salt hypertension in rats, a model for an upregulated endothelin-1 system. Mesenteric small arteries (MrA) were exposed to low blood flow (LF) or high blood flow (HF) for 4 or 7 weeks. The bioavailability of vasoactive peptides was modified by chronic treatment of the rats with the dual neutral endopeptidase (NEP)/endothelin-converting enzyme (ECE) inhibitor SOL1. After 3 or 6 weeks of hypertension, the MrA showed hypertrophic arterial remodeling (3 weeks: media cross-sectional area (mCSA): 10 +/- 1 x 10(3) to 17 +/- 2 x 10(3) mu m(2); 6 weeks: 13 +/- 2 x 10(3) to 24 +/- 3 x 10(3) mu m(2)). After 3, but not 6, weeks of hypertension, the arterial diameter was increased (empty set: 385 +/- 13 to 463 +/- 14 mu m). SOL1 reduced hypertrophy after 3 weeks of hypertension (mCSA: 6 x 10(3) +/- 1 x 10(3) mu m(2)). The diameter of the HF arteries of normotensive rats increased (empty set: 463 +/- 22 mu m) but no expansion occurred in the HF arteries of hypertensive rats (empty set: 471 +/- 16 mu m). MrA from SOL1-treated hypertensive rats did show a significant diameter increase (empty set: 419 +/- 13 to 475 +/- 16 mu m). Arteries exposed to LF showed inward remodeling in normotensive and hypertensive rats (mean empty set between 235 and 290 mu m), and infiltration of monocyte/ macrophages. SOL1 treatment did not affect the arterial diameter of LF arteries but reduced the infiltration of monocyte/ macrophages. We show for the first time that flow-induced remodeling is impaired during the development of DOCA-salt hypertension and that this can be prevented by chronic NEP/ECE inhibition. Hypertension Research (2012) 35, 1093-1101; doi:10.1038/hr.2012.94; published online 12 July 201
Collateral circulation: Past and present
Following an arterial occlusion outward remodeling of pre-existent inter-connecting arterioles occurs by proliferation of vascular smooth muscle and endothelial cells. This is initiated by deformation of the endothelial cells through increased pulsatile fluid shear stress (FSS) caused by the steep pressure gradient between the high pre-occlusive and the very low post-occlusive pressure regions that are interconnected by collateral vessels. Shear stress leads to the activation and expression of all NOS isoforms and NO production, followed by endothelial VEGF secretion, which induces MCP-1 synthesis in endothelium and in the smooth muscle of the media. This leads to attraction and activation of monocytes and T-cells into the adventitial space (peripheral collateral vessels) or attachment of these cells to the endothelium (coronary collaterals). Mononuclear cells produce proteases and growth factors to digest the extra-cellular scaffold and allow motility and provide space for the new cells. They also produce NO from iNOS, which is essential for arteriogenesis. The bulk of new tissue production is carried by the smooth muscles of the media, which transform their phenotype from a contractile into a synthetic and proliferative one. Important roles are played by actin binding proteins like ABRA, cofilin, and thymosin beta 4 which determine actin polymerization and maturation. Integrins and connexins are markedly up-regulated. A key role in this concerted action which leads to a 2-to-20 fold increase in vascular diameter, depending on species size (mouse versus human) are the transcription factors AP-1, egr-1, carp, ets, by the Rho pathway and by the Mitogen Activated Kinases ERK-1 and -2. In spite of the enormous increase in tissue mass (up to 50-fold) the degree of functional restoration of blood flow capacity is incomplete and ends at 30% of maximal conductance (coronary) and 40% in the vascular periphery. The process of arteriogenesis can be drastically stimulated by increases in FSS (arterio-venous fistulas) and can be completely blocked by inhibition of NO production, by pharmacological blockade of VEGF-A and by the inhibition of the Rho-pathway. Pharmacological stimulation of arteriogenesis, important for the treatment of arterial occlusive diseases, seems feasible with NO donors
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