STRUCTURE AND PROPERTIES OF NANOSIZE NiFe2O4 PREPARED BY TEMPLATE AND PRECIPITATION METHODS

Nanosize NiFe2O4 was prepared by template method and precipitation process using same starting materials. The use of soluble starch in both synthesis routes was investigated. The amount of the used precipitating agent (Na2CO3) for the precipitation approach was selected according to two adopted scenarios based on theoretical and average yield of possible side reaction expressed by the degree of substitution (DS). The results of SEM microstructural analysis of the prepared Ni-ferrite powders demonstrate evident influence of the applied preparation method whereas high-magnification FE-SEM images show very similar fine-grained structures characterized by different size of particles. According to the results of XRD analysis, the obtained ferrite powders exhibit only slight differences in phase composition with calculated crystallite size for template sample d(XRD) = 36 nm and for the both precipitation route samples d(XRD) = 21 nm. Additional sample characterization using Fe-57 Mossbauer spectroscopy supports the findings of the microstructural and XRD analysis. The "clearest" spectrum was obtained for the template sample while the strongest influence of nanocrystalline component was observed for the sample prepared with maximal amount of precipitation agent (DS=3). The room temperature magnetic hysteresis loops, recorded using vibrating sample magnetometer (VSM), are very similar and exhibit characteristic shape with values of magnetic properties within expected range for this type of material

Nanocomposite permanent magnetic materials Nd-Fe-B type: The influence of nanocomposite on magnetic properties

The influence on the magnetic properties of nanocristalline ribbons and powders has character of microstructure, between others – the grain size volume of hard and soft magnetic phases and their distribution. Magnetic properties of ribbons and powders depend mainly on their chemical composition and parameters of their heat treatment [1]. Technology of magnets from nanocristalline ribbon consists of the following process: preparing the Nd-Fe- B alloy, preparing the ribbon, powdering of the ribbon, heat treatment of the powder and finally preparing the magnets. Nanocomposite permanent magnet materials based on Nd-Fe- B alloy with Nd low content are a new type of permanent magnetic material. The microstructure of this nanocomposite permanent magnet is composed of a mixture of magnetically soft and hard phases which provide so called exchange coupling effect

Thermomagnetic Analysis of Nanocrystalline Nd4.5Fe77B18.5 Alloy

Changes in the phase composition and crystallite size of a rapid quenched Nd4.5Fe77B18.5 alloy, caused by thermomagnetic measurements (TM) have been studied using XRD methods of phase analysis. crystallite size and lattice microstrain determination. Structural changes in regard to optimal magnetic state were additionally analyzed by TEM. Magnetic properties in optimal magnetic state and after TM were observed using room temperature SQUID measurements. The obtained experimental results suggest the Fe3B/Nd2Fe14B and partly alpha-Fe nanocomposite structure of the alloy in the optimized magnetic state. with mean crystallite size (< 30nm). After TM. an increased amount of alpha-Fe phase, presence of different oxide and Fe-B phases as well as growth of crystallites are found to be the main reasons for the observed quality loss of hard magnetic properties.close4

Influence of Short Central PEO Segment on Hydrolytic and Enzymatic Degradation of Triblock PCL Copolymers

Hydrolytic, enzymatic degradation and composting under controlled conditions of series of triblock PCL/PEO copolymers, PCEC, with central short PEO block (M (n) 400 g/mol) are presented and compared with homopolymer (PCL). The PCEC copolymers, synthesized via ring-opening polymerization of epsilon-caprolactone, were characterized by H-1 NMR, quantitative C-13 NMR, GPC, DSC and WAXS. The introduction of the PEO central segment ( lt 2 wt%) in PCL chains significantly affected thermal degradation and crystallization behavior, while the hydrophobicity was slightly reduced as confirmed by water absorption and moisture uptake experiments. Hydrolytic degradation studies in phosphate buffer after 8 weeks indicated a small weight loss, while FTIR analysis detected changes in crystallinity indexes and GPC measurements revealed bulk degradation. Enzymatic degradation tested by cell-free extracts containing Pseudomonas aeruginosa PAO1 confirmed high enzyme activity throughout the surface causing morphological changes detected by optical microscopy and AFM analysis. The changes in roughness of polymer films revealed surface erosion mechanism of enzymatic degradation. Copolymer with the highest content of PEO segment and the lowest molecular weight showed better degradation ability compared to PCL and other copolymers. Furthermore, composting of polymer films in a model compost system at 37 A degrees C resulted in significant degradation of the all synthesized block copolymers