Continuous size fractionation of magnetic nanoparticles by using simulated moving bed chromatography

The size fractionation of magnetic nanoparticles is a technical problem, which until today can only be solved with great effort. Nevertheless, there is an important demand for nanoparticles with sharp size distributions, for example for medical technology or sensor technology. Using magnetic chromatography, we show a promising method for fractionation of magnetic nanoparticles with respect to their size and/or magnetic properties. This was achieved by passing magnetic nanoparticles through a packed bed of fine steel spheres with which they interact magnetically because single domain ferro-/ferrimagnetic nanoparticles show a spontaneous magnetization. Since the strength of this interaction is related to particle size, the principle is suitable for size fractionation. This concept was transferred into a continuous process in this work using a so-called simulated moving bed chromatography. Applying a suspension of magnetic nanoparticles within a size range from 20 to 120 nm, the process showed a separation sharpness of up to 0.52 with recovery rates of 100%. The continuous feed stream of magnetic nanoparticles could be fractionated with a space-time-yield of up to 5 mg/(L·min). Due to the easy scalability of continuous chromatography, the process is a promising approach for the efficient fractionation of industrially relevant amounts of magnetic nanoparticles

Influence of the hierarchical architecture of multi-core iron oxide nanoflowers on their magnetic properties

Magnetic properties of superparamagnetic iron oxide nanoparticles are controlled mainly by their particle size and by their particle size distribution. Magnetic properties of multi-core iron oxide nanoparticles, often called iron oxide nanoflowers (IONFs), are additionally affected by the interaction of magnetic moments between neighboring cores. The knowledge about the hierarchical structure of IONFs is therefore essential for understanding the magnetic properties of IONFs. In this contribution, the architecture of multi-core IONFs was investigated using correlative multiscale transmission electron microscopy (TEM), X-ray diffraction and dynamic light scattering. The multiscale TEM measurements comprised low-resolution and high-resolution imaging as well as geometric phase analysis. The IONFs contained maghemite with the average chemical composition -Fe$_{2.72±0.02}$O$_{4}$. The metallic vacancies located on the octahedral lattice sites of the spinel ferrite structure were partially ordered. Individual IONFs consisted of several cores showing frequently a specific crystallographic orientation relationship between direct neighbors. This oriented attachment may facilitate the magnetic alignment within the cores. Individual cores were composed of partially coherent nanocrystals having almost the same crystallographic orientation. The sizes of individual constituents revealed by the microstructure analysis were correlated with the magnetic particle sizes that were obtained from fi

Magnetoresistance and structural study of electrodeposited Ni-Cu/Cu multilayers

Electrodeposition was used to produce Ni Cu/Cu multilayers by two-pulse plating (galvanostatic/potentiostatic control) from a single sulfate/sulfamate electrolyte at an optimized Cu deposition potential for the first time. Magnetoresistance measurements were carried out at room temperature for the Ni Cu/Cu multilayers as a function of the Ni Cu and Cu layer thicknesses and the electrolyte Cu2+ ion concentration. Multilayers with Cu layer thicknesses above 2 nm exhibited a giant magnetoresistance (GMR) effect with a dominating ferromagnetic contribution and with low saturation fields (below 1 kOe). A significant contribution from superparamagnetic (SPM) regions with high saturation fields occurred only for very small nominal magnetic layer thicknesses (around 1 nm). The presence of SPM regions was concluded from the GMR data also for thick magnetic layers with high Cu contents. This hints at a significant phase-separation in Ni-Cu alloys at low-temperature processing, in agreement with previous theoretical modeling and experiments. Low-temperature measurements performed on a selected multilayer down to 18 K indicated a strong increase of the GMR as compared to the room-temperature GMR. Structural studies of some multilayer deposits exhibiting GMR were performed by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The XRD patterns of Ni Cu/Cu multilayers exhibited in most cases clear satellite peaks, indicating a superlattice structure which was confirmed also by cross-sectional TEM. The deterioration of the multilayer structure revealed by XRD for high Cu-contents in the magnetic layer confirmed the phase-separation concluded from the GMR data

Face Centred Cubic Multi-Component Equiatomic Solid Solutions in the Au-Cu-Ni-Pd-Pt System

A single-phase solid solution is observed in quaternary and quinary alloys obtained from gold, copper, nickel, palladium and platinum. The lattice parameters of the alloys follow the linear rule of mixture when considering the lattice parameters of the elements and their concentration. The elements are a priori not homogeneously distributed within the respective alloys resulting in segregations. These segregations cause a large broadening of X-ray lines, which is accessed in the present article. This correlation is visualized by the help of local element mappings utilizing scanning electron microscopy including energy dispersive X-ray analysis and their quantitative analysis

Face Centred Cubic Multi-Component Equiatomic Solid Solutions in the Au-Cu-Ni-Pd-Pt System

A single-phase solid solution is observed in quaternary and quinary alloys obtained from gold, copper, nickel, palladium and platinum. The lattice parameters of the alloys follow the linear rule of mixture when considering the lattice parameters of the elements and their concentration. The elements are a priori not homogeneously distributed within the respective alloys resulting in segregations. These segregations cause a large broadening of X-ray lines, which is accessed in the present article. This correlation is visualized by the help of local element mappings utilizing scanning electron microscopy including energy dispersive X-ray analysis and their quantitative analysis

Influence of Ag additive to the spacer layer on the structure and giant magnetoresistance of electrodeposited Co/Cu multilayers

In order to explore the possible surfactant effect of Ag on the formation of electrodeposited multilayers, Co/Cu(Ag) multilayers were prepared by this technique and their structure and giant magnetoresistance (GMR) were investigated. The multilayers were deposited from a perchlorate bath with various amounts of Ag+ ions in the solution for incorporating Ag atoms into the multilayer stack. Without Ag addition, secondary neutral mass spectroscopy (SNMS) indicated a well-defined composition modulation of the undermost Co/Cu bilayers. However, already at an Ag content as low as 1.8 at.% incorporated, SNMS showed a deterioration of the periodic multilayer structure. In agreement with the SNMS results, superlattice satellites were visible in the X-ray diffraction (XRD) patterns of the multilayers with up to 0.3 at.% Ag. The satellites were, however, very faint even for multilayers without Ag addition, indicating that the multilayers have high interface roughness and/or poor periodicity. In the absence of Ag and at the smallest Ag content investigated by XRD, a strong central multilayer peak and the weak superlattice satellites were complemented by weak diffraction maxima from non-periodic Co and Cu domains. In the Co/Cu(Ag) multilayer containing about 25 at.% Ag, i.e., nearly as much as Cu, XRD found a separate Ag(Cu) phase. In spite of the imperfect layered structure, a multilayer-type GMR behavior was observed in all samples up to about 10 at.% Ag incorporated in the multilayer stack. The GMR magnitude increased for Ag contents up to about 1 at.%, which implies that a small amount of Ag may have a beneficial effect through a slight modification of the layer growth and/or interface formation. However, for higher Ag contents beyond this level, the GMR was reduced in line with the structural degradation revealed by XRD and SNMS. For the highest Ag contents (above about 10 at.%), the GMR exhibited a behavior characteristic of a granular magnetic alloy, in agreement with the results of the structural study

Shock-induced plasticity in nanocrystalline iron: Large-scale molecular dynamics simulations

Large-scale nonequilibrium molecular dynamics (MD) simulations of shock waves in nanocrystalline iron show evidence of plasticity before the polymorphic transformation takes place. The atomistic structure in the shock direction shows an elastic precursor, plastic deformation, and shock-induced phase transformation from bcc to hcp iron. In this Rapid Communication, large-scale MD models show that the shock response of iron is highly related to the ramp time of the applied shocks. For long ramp times we observe significant plastic relaxation and formation of microstructure defects. Pressure-induced phase transformations in iron are accompanied by stress relaxation achieving almost fully relaxed three-dimensional hydrostatic final states. The evolution of the stress relaxation is in agreement with theory and experiments. Analysis of the x-ray diffraction patterns calculated from the atomistic structure using the Debye equation revealed pronounced anisotropy of the line broadening that is caused by stacking faults in hcp Fe and by dislocations in bcc Fe.Fil: Luu, Hoang Thien. Clausthal University of Applied Technology; AlemaniaFil: Ravelo, Ramón. University of Texas at El Paso; Estados UnidosFil: Rudolph, Martin. TU Bergakademie Freiberg; AlemaniaFil: Bringa, Eduardo Marcial. Universidad de Mendoza; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Germann, Timothy C.. Los Alamos National High Magnetic Field Laboratory; Estados UnidosFil: Rafaja, David. TU Bergakademie Freiberg; AlemaniaFil: Gunkelmann, Nina. Clausthal University of Applied Technology; Alemani

Hematites precipitated in alkaline precursors: Comparison of structural and textural properties for methane oxidation

Hematite (alpha-Fe2O3) catalysts prepared using the precipitation methods was found to be highly effective, and therefore, it was studied with methane (CH4), showing an excellent stable performance below 500 degrees C. This study investigates hematite nanoparticles (NPs) obtained by precipitation in water from the precursor of ferric chloride hexahydrate using precipitating agents NaOH or NH4OH at maintained pH 11 and calcined up to 500 degrees C for the catalytic oxidation of low concentrations of CH4 (5% by volume in air) at 500 degrees C to compare their structural state in a CH4 reducing environment. The conversion (%) of CH4 values decreasing with time was discussed according to the course of different transformation of goethite and hydrohematites NPs precursors to magnetite and the structural state of the calcined hydrohematites. The phase composition, the size and morphology of nanocrystallites, thermal transformation of precipitates and the specific surface area of the NPs were characterized in detail by X-ray powder diffraction, transmission electron microscopy, infrared spectroscopy, thermal TG/DTA analysis and nitrogen physisorption measurements. The results support the finding that after goethite dehydration, transformation to hydrohematite due to structurally incorporated water and vacancies is different from hydrohematite alpha-Fe2O3. The surface area SBET of Fe2O3_NH-70 precipitate composed of protohematite was larger by about 53 m(2)/g in comparison with Fe2O3_Na-70 precipitate composed of goethite. The oxidation of methane was positively influenced by the hydrohematites of the smaller particle size and the largest lattice volume containing structurally incorporated water and vacancies.Web of Science2315art. no. 816

Boxnep - модульный подводный робот перспективных технологий

The article discusses the relevance of the underwater vehicles are able to solve a wide range of problems. The decision puts in a basis of the research is designing a modular underwater robot. It allows to make a mounting of various equipment and testing it in the water medium. The paper deals with the concept of the robot and its characteristics

Spider chitin: An Ultrafast Microwave-Assisted Method for Chitin Isolation from Caribena versicolor Spider Molt Cuticle

Chitin, as a fundamental polysaccharide in invertebrate skeletons, continues to be actively investigated, especially with respect to new sources and the development of effective methods for its extraction. Recent attention has been focused on marine crustaceans and sponges; however, the potential of spiders (order Araneae) as an alternative source of tubular chitin has been overlooked. In this work, we focused our attention on chitin from up to 12 cm-large Theraphosidae spiders, popularly known as tarantulas or bird-eating spiders. These organisms “lose” large quantities of cuticles during their molting cycle. Here, we present for the first time a highly effective method for the isolation of chitin from Caribena versicolor spider molt cuticle, as well as its identification and characterization using modern analytical methods. We suggest that the tube-like molt cuticle of this spider can serve as a naturally prefabricated and renewable source of tubular chitin with high potential for application in technology and biomedicine. © 2019 by the authors