RESUMEN
The current study attempts to establish the interrelation between microstructure and magnetic properties induced during laser melting of the FeNi alloy. This study demonstrates the optimization of laser parameters for defect-free, uniform, and chemically homogeneous FeNi alloy synthesis. Mechanically alloyed FeNi (50-50 atom %) powders obtained after 12 and 24 h milling, with average particle sizes of 15 and 7 µm, were used as starting materials. It was found that the optimum range of laser power density for synthesis of dense and defect-free solids is between 1 and 1.4 J/mm2. For laser melting under similar conditions, 12 h milled FeNi powder produces a larger grain (â¼100 µm) with a preferred texture of (001), compared to 25 µm grain size in 24 h milled FeNi, with random texture. Smaller grain size is correlated with higher resistance to domain wall movement, resulting in higher coercivity and remanence in the laser-melted samples prepared from 24 h of milled powder. The presence of microtexture in laser-melted samples prepared from 12 h milled powder is related to a higher anisotropy.
RESUMEN
L10-ordered FeNi, tetrataenite, found naturally in meteorites is a predilection for next-generation rare-earth free permanent magnetic materials. However, the synthesis of this phase remains unattainable in an industrially relevant time frame due to the sluggish diffusion of Fe and Ni near the order-disorder temperature (593 K) of L10 FeNi. The present work describes the synthesis of ordered L10 FeNi from elemental Fe and Ni powders by mechanical alloying up to 12 h and subsequent heat treatment at 623 K for 1000 h without a magnetic field and for 4 h in the presence of 1.5 T magnetic field. Also, to address the ambiguity of L10 phase identification caused by the low difference in the X-ray scattering factor of Fe and Ni, synchrotron-based X-ray diffraction is employed, which reveals that 6 h milling is sufficient to induce L10 FeNi formation. Further milling for 12 h is done to achieve a chemically homogeneous powder. The phase fraction of L10-ordered FeNi is quantified to â¼9 wt % for 12 h milled FeNi, which increases to â¼15 wt % after heat treatment. Heat treatment of the milled powder in a magnetic field increases the long-range order parameter (S) from 0.18 to 0.30. Further, the study of magnetic properties reveals a decrease in magnetic saturation and a slight increase in coercivity with the increase in milling duration. At the same time, heat treatment in the magnetic field shows a considerable increase in coercivity.
RESUMEN
The pristine Human Amniotic Membrane (HAM) has portrayed outstanding potential as scaffold for ocular surface reconstruction and regeneration. However, in treatment procedures where the supporting membrane matrix of HAM is not obligatory and only the bioactive molecules are vital, the surgical practise of HAM grafting causes redundant trauma and economic burden to the patient. Hence, in our laboratory we have attempted to break down HAM to nanoscale particles and validate its potential as a competent ocular therapeutic agent; by conducting a comparative analysis between the fresh, lyophilized, micronized and Nanonized Amniotic Membrane (NAM) particles. Our results evidently showcased that the prepared NAM particles was <100 nm and the major biomolecules such as collagen and hyaluronic acid were well retained. Further, the NAM particles eluted significantly higher amounts of proteins and growth factors while maintaining its stability and isotonicity when stored at 4 °C. Its biostability was assayed in the presence of lysozyme enzyme. Its remarkable ability to promote cell proliferation in rabbit corneal cells and negative cytotoxicity is an added advantage for ocular application. The ocular biocompatibility of NAM, evaluated by the ex vivo assessment of corneal thickness, transparency, histopathology, immunohistochemistry and corneal permeability clearly indicated its suitability for ophthalmic applications.