Effect of Temperature on Microwave Permeability of an Air-Stable Composite Filled with Gadolinium Powder

A composite containing about 30% volume of micrometer-size powder of gadolinium in paraffin wax is synthesized mechanochemically. The composite permittivity and permeability are measured within the frequency range from 0.01 to 15 GHz and the temperature range from ~0 °C to 35 °C. The permittivity is constant within the measured ranges. Curie temperature of the composite is close to 15.5 °C, the phase transition is shown to take place within a temperature range about ±10 °C. The effect of temperature deviation from Curie point on reflection and transmission of a composite layer filled with Gd powder is studied experimentally and via simulation. Constitutive parameters of the composite are measured in cooled coaxial lines applying reflection-transmission and open-circuit-short-circuit techniques, and the measured low-frequency permeability is in agreement with the values retrieved from the published magnetization curves. The effect of temperature on permeability spectrum of the composite is described in terms of cluster magnetization model based on the Wiener mixing formula. The model is applied to design a microwave screen with variable attenuation; the reflectivity attenuation of 4.5 mm-thick screen increases from about −2 dB to −20 dB at 3.5 GHz if the temperature decreases from 25 °C to 5 °C

Frequency dependence of microwave complex permeability under magnetic bias

Measurement of the frequency dependence of the permeability under magnetic bias is proposed as a new method for studying the microwave magnetic properties of magnetic materials. The samples under study are either rolls of thin ferromagnetic films or the composites filled with sendust particles. It is shown that the permeability measured under external magnetic bias depends on sample thickness. The correct interpretation of the measured data is possible only when sample demagnetization is accounted for. The values of the anisotropy field and the saturation magnetization of thin nitrogen doped iron films and flake-shaped sendust particles are calculated considering demagnetization of the washer-shaped sample

Frequency dependence of microwave complex permeability under magnetic bias

Measurement of the frequency dependence of the permeability under magnetic bias is proposed as a new method for studying the microwave magnetic properties of magnetic materials. The samples under study are either rolls of thin ferromagnetic films or the composites filled with sendust particles. It is shown that the permeability measured under external magnetic bias depends on sample thickness. The correct interpretation of the measured data is possible only when sample demagnetization is accounted for. The values of the anisotropy field and the saturation magnetization of thin nitrogen doped iron films and flake-shaped sendust particles are calculated considering demagnetization of the washer-shaped sample

Deposition of Thick SiO2 Coatings to Carbonyl Iron Microparticles for Thermal Stability and Microwave Performance

Thick dielectric SiO2 shells on the surface of iron particles enhance the thermal and electrodynamic parameters of the iron. A technique to deposit thick, 500-nm, SiO2 shell to the surface of carbonyl iron (CI) particles was developed. The method consists of repeated deposition of SiO2 particles with air drying between iterations. This method allows to obtain thick dielectric shells up to 475 nm on individual CI particles. The paper shows that a thick SiO2 protective layer reduces the permittivity of the ‘Fe-SiO2—paraffin’ composite in accordance with the Maxwell Garnett medium theory. The protective shell increases the thermal stability of iron, when heated in air, by shifting the transition temperature to the higher oxide. The particle size, the thickness of the SiO2 shells, and the elemental analysis of the samples were studied using a scanning electron microscope. A coaxial waveguide and the Nicholson–Ross technique were used to measure microwave permeability and permittivity of the samples. A vibrating-sample magnetometer (VSM) was used to measure the magnetostatic data. A synchronous thermal analysis was applied to measure the thermal stability of the coated iron particles. The developed samples can be applied for electromagnetic compatibility problems, as well as the active material for various types of sensors

Deposition of Thick SiO₂ Coatings to Carbonyl Iron Microparticles for Thermal Stability and Microwave Performance

Thick dielectric SiO2 shells on the surface of iron particles enhance the thermal and electrodynamic parameters of the iron. A technique to deposit thick, 500-nm, SiO2 shell to the surface of carbonyl iron (CI) particles was developed. The method consists of repeated deposition of SiO2 particles with air drying between iterations. This method allows to obtain thick dielectric shells up to 475 nm on individual CI particles. The paper shows that a thick SiO2 protective layer reduces the permittivity of the ‘Fe-SiO2—paraffin’ composite in accordance with the Maxwell Garnett medium theory. The protective shell increases the thermal stability of iron, when heated in air, by shifting the transition temperature to the higher oxide. The particle size, the thickness of the SiO2 shells, and the elemental analysis of the samples were studied using a scanning electron microscope. A coaxial waveguide and the Nicholson–Ross technique were used to measure microwave permeability and permittivity of the samples. A vibrating-sample magnetometer (VSM) was used to measure the magnetostatic data. A synchronous thermal analysis was applied to measure the thermal stability of the coated iron particles. The developed samples can be applied for electromagnetic compatibility problems, as well as the active material for various types of sensors

Influence of Hydrogen Reduction Stage Conditions on the Microwave Properties of Fine Iron Powders Obtained via a Spray-Pyrolysis Technique

The relationship between the chemical purity of one-size particles and microwave properties in ferromagnetic materials is not clearly studied. Ferromagnetic nanostructured iron powders were synthesized from iron nitrate solution using ultrasonic spray-pyrolysis and then reduced in H2 flow at 350, 400, 450, and 500 °C. A rise in the concentration of solutions of a precursor from 10 to 20 wt. % led to an increase in mean particle size. The interrelationship was studied between chemical composition and the microwave dispersion of the powders obtained. An increase in the temperature of reduction changes the chemical composition and increases the amplitude of complex microwave permeability, which was studied using solid-state physics methods (XRD, STA, SEM, and VNA). It was found that annealing at 400 °C is the optimal treatment that allows the production of iron powders, consisting of about 90% of α-Fe phase, possessing a particle surface with low roughness and porosity, and demonstrating intense microwave absorption. Annealing at a higher temperature (500 °C) causes an even higher increase in permeability but leads to the destruction of nanostructured spheres into smaller particles due to grain growth. This destruction causes an abrupt increase in permittivity and therefore significantly reduces potential applications of the product. The insight into chemical–magnetic relationships of these materials enhances the data for design applications in magnetic field sensing

Synthesis and Structure of 6-Acetyl-2-Arylhydrazone Derivatives of Thiazolo[3,2-<i>a</i>]Pyrimidine

Triazolo[4,3-a]pyrimidine is one of the promising structural fragments for the development of drugs, including anticancer drugs. This work is devoted to the synthesis of a number of new 2-arylhydrazone derivatives of thiazolo[3,2-a]pyrimidine, which are synthetic precursors for triazolo[4,3-a]pyrimidines. The crystal structure of 6-acetyl-7-methyl-5-phenyl-2-(2-phenylhydrazineylidene)-5H-thiazolo[3,2-a]pyrimidin-3(2H)-one was established by SCXRD. In the reduction reaction of the compound, the following system was used: vanadium(V) oxide, and sodium borohydride in ethanol at room temperature, which led to the formation of only one pair of diastereomers (1R*)-1-((5S*,6R*,7R*)-(1-(hydroxymethyl)-7-methyl-1,5-diphenyl-1,5,6,7-tetrahydro[1,2,4]triazolo[4,3-a]pyrimidin-6-yl)ethan-1-ol