Strontium Hexaferrite Research Articles

Synthesis and Characterization of Cu-Co Substituted Strontium Hexaferrite for Magnetic Applications

In this study, the structural and magnetic characterizations of a series of SrCoxCuxFe12-2xO19; 0.0 ≤ x ≤ 0.5 samples, which were produced by the conventional ceramic method, were carried out. The structure was examined by X-ray diffraction (XRD) technique and optical microscopy. A vibrating sample magnetometer (VSM) was used to characterize the ferrimagnetic properties. XRD patterns confirmed the presence of a single phase as Sr-hexaferrite while there were not any peaks of unreacted Fe2O3 phase. The densities varied between 92 – 98 %. XRD patterns of the Sr-hexaferrite samples were slightly modified because of the co-substitution of Cu-Co; however, the magnetic properties changed remarkably. The sample with Cu-Co of x = 0.1 content had the highest saturation magnetization (33.52 emu/g), remanence (19.74 emu/g), and coercivity (4.3 kOe). The synthesized magnetic samples were found to be suitable for the development of attractive ferrimagnetic properties for the current ferrite magnets.

Tailoring of Structural, Electrical, Optical and Impedance Characteristics of Co2+ and Zr4+ Doped Strontium Hexaferrites

Tailoring of Structural, Electrical, Optical and Impedance Characteristics of Co2+ and Zr4+ Doped Strontium Hexaferrites

Doping effects in strontium hexaferrite: Theoretical and experimental analysis

Hexagonal ferrites based on SrFe12O19 (SFO) are vital materials in the field of permanent magnets, valued for their cost-effectiveness and reliable magnetic properties, making them a more affordable alternative to rare-earth permanent magnets. This study focuses on understanding the doping effects of commonly used elements in SFO system. DFT calculation results show that doping La or La-Co can enhance the phase stability of SFO, in which Co has a preference for the 4f1 sites of Fe. The total magnetic moment was observed to slightly decrease with La doping, whereas it exhibited an increasing trend with La-Co and La-Ca-Co co-doping and the largest increase of 6.5 % can be obtained in Sr2LaCaFe44Co4O76 (SLCFCO). The increase in the total magnetic moment is mainly attributed to the smaller antiferromagnetic moment of Co than that of Fe on 4f1 sites, as well as the reduction in the antiferromagnetic Fe moments at 4f1 and 4f2 sites. The total density of states indicates a transition from semiconductor behavior to a metallic character both in the La-Co and La-Ca-Co doped versions. The experimental results validate the theoretical predictions, confirming enhancements in magnetic performance. The saturation magnetization increased from 63.86 Am2/kg in SrFe11.7O19 (SFO) to 67.53 Am2/kg in Sr0.4La0.4Ca0.2Fe10.5Co0.5O19 composition. These findings provide a vital understanding of tuning the magnetic and electronic properties in doped SFO, which will enable the development of advanced applications in magnetic materials.

Tailoring SrFe12O19 – MoS2 composites for enhanced microwave absorption performance in X-band

The electromagnetic wave-absorbing composites, incorporating strontium hexaferrite and molybdenum disulfide (SrFe12O19-MoS2), are synthesized by mixing in different weight ratios. In the present work, strontium hexaferrite (SrFe12O19) is developed through a low-temperature auto-combustion method while two-dimensional molybdenum disulfide (MoS2) is synthesized by a facile hydrothermal process. The materials and their composites undergo analysis using characterization techniques such as X-ray diffraction (XRD), fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), and vibrating sample magnetometer (VSM) to assess their structural, morphological, and magnetic properties, respectively. The minimal reflection loss (RLmin) of – 47.35 dB is observed at 8.66 GHz for the SrFe12O19-MoS2 (50 %-50 %) composite cast into pellets for microwave absorption analysis in the X-band frequency range. This RLmin is obtained with a sample thickness of 1.7 mm. An adequate bandwidth of 3.1 GHz, representing 77.5 % of the entire X band, is observed for a loss below −10 dB. The synergistic interaction between magnetism and dielectricity makes it an efficient electromagnetic absorber for modern technologies.

Electrochemical hydrogen storage using SrFe12O19 surface-immobilized polyoxometalate

A tri-nickel substituted Keggin-type polyoxometalate (PMo9Ni3O37) was synthesized and subsequently immobilized on the surface of the M-type strontium hexaferrite (SrFe12O19) via the sol-gel method. The investigation of hydrogen storage capacity for the synthesized PMo9Ni3O37@SrFe12O19 nanocomposite was conducted through electrochemical methodologies employing chronopotentiometry (CP). A conventional three-electrode configuration employing copper foam coated with PMo9Ni3O37@SrFe12O19 served as the working electrode and was examined across a current range of ±1.5 mA. The charge and discharge of the experimental procedure indicated the substantial potential of the PMo9Ni3O37@SrFe12O19 nanocomposite in the hydrogen storage process, which was determined 3125 mAh/g during the discharge phase. The successful synthesis was corroborated thorough FT-IR, UV-vis, XRD, SEM, EDX, and BET surface area analysis techniques by examining the characteristic absorption wavelengths or reflection patterns. The size of the nanoparticles was determined through SEM analysis yielding a diameter of 36.76 nm, and using the Scherrer equation, a diameter of 29.22 nm was obtained.

Effect of microwave sintering on density, microstructural and magnetic properties of pure strontium hexaferrite at low temperatures and heating rate

In recent decades, the rising demand for permanent magnetic materials has driven manufacturers to explore substitutes for rare earth elements in response to their fluctuating prices and negative environmental impact. M-type hexaferrites considered as good alternatives and studies have focused on enhancing their magnetic and structural properties through various approaches. In this study, new approach using low heating rate microwave sintering has been applied to investigate the changes on density, microstructure, and magnetic properties of strontium hexaferrite from core to surface. Sintering temperatures of 950 °C, 1000 °C, 1050 °C, and 1100 °C with 10 °C/minute heating rate were applied accordingly. The bulk density, FESEM, XRD and VSM tests were conducted to study materials’ properties. The outcomes of the study showed exponential relationship between density and sintering temperature reaching optimum value of 91.4 % at 1050 °C and then declined slightly at observed to analysis confirmed the magnetoplumbite structure P63/mmc in all samples and high crystallized structure at 1050 °C, with the occurrence of α-Fe2O3 at 1100 °C. Grain growth and crystallization observed to increase at higher sintering temperature with agglomeration while denser and melted boundaries at lower temperatures. Magnetic properties especially remanence magnetization Mr and saturation magnetization Ms fluctuated with sintering temperature achieving optimum values of 28.188 emu/g and 55.622 emu/g at 1000 °C respectively. Coercivity Hc and magnetic energy density BH max recorded optimum values at 1050 °C. The findings emphasize the critical role of microwave sintering in tailoring the properties of strontium hexaferrite for magnetic applications.

Effect of 10 MeV electron irradiation on structural and magnetic properties of Ti- and Al- substituted strontium hexaferrite SrFe11.3Ti0.4Al0.3O19

The irradiation stability of Ti- and Al-substituted SrFe11.3Ti0.4Al0.3O19 strontium hexaferrite to 10 MeV electron irradiation with the fluences of 1014 and 2·1017 cm−2 was investigated using various characterization techniques such as scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectrum microanalysis, atomic force microscopy, Raman spectroscopy, vibrating sample magnetometry and magnetic force microscopy. Notable changes in lattice vibrations, magnetic domain microstructure and magnetization behavior were obtained after the electron irradiation with the fluence of 2·1017 cm−2. Phonon hardening observed by Raman spectroscopy confirms the increasing disorder in crystalline structure and the presence of spin-phonon coupling in the samples after electron irradiation with the fluence 2·1017 cm−2. It was found that the strongest spin-phonon interactions correspond to A1g vibration modes at trigonal bipyramidal 2b, 2a octahedral, 4f1 tetrahedral sites and E1g mode at 4f2 octahedral site in electron-irradiated SrFe11.3Ti0.4Al0.3O19 hexaferrite, while the most radiation-resistant phonon mode is A1g vibration of the Fe–O bonds at the 4f2 octahedral site. No significant change was observed in magnetic saturation magnitude after electron irradiation. The increase in coercivity and significant decrease of magnitude of the dM/dH derivative of magnetization curves with increasing radiation fluence is attributed to the increase in uniaxial magnetic-crystalline anisotropy. It is found that the fractal dimension of hierarchical magnetic domain structure in SrFe11.3Ti0.4Al0.3O19 continuously decreases with increasing fluence of 10 MeV electron irradiation, which can be caused by the distortion in uniaxial magnetocrystalline anisotropy and irradiation-induced defects.

Magneto-fluorescent core–shell Sr0.8La0.2Fe11CuO19 @ CQDs for the detection of metal ions

The fabrication of a sensor based on a core–shell structure of Sr0.8La0.2Fe11CuO19 @ CQDs was effectively achieved through the combination of high quantum yield carbon quantum dots (CQDs) with La-Cu doped M−type strontium hexaferrites (SLFCO HF). The structural, morphological, and spectroscopic information of the as-synthesized samples were characterized through X-ray diffraction (XRD), Raman spectroscopy (RS), Fourier transform infrared (FT-IR), energy dispersive X-ray (EDX), high-resolution transmission electron microscopy (HR-TEM), and UV–Vis-NIR spectroscopy. The magnetic properties were tested using a vibrating sample magnetometer (VSM) and Mössbauer spectroscopy. HR-TEM confirmed the formation of a hexagonal core–shell sample at the nanoscale. Based on photoluminescence (PL) spectra and the CIE chromaticity map, the parent sample and core–shell structure of SLFCO/CQDs were found to have color coordinates corresponding to yellow-green emission. It was found that the core–shell sample has an increased light-absorption capacity, low photogenerated electron-hole recombination, high coercivity, small crystallite size, and showed good sensitivity towards the detection of Zn2+, Cd2+, and K+ ions. A high efficiency in detecting potassium (K+) ions with a limit of detection (LOD) of 15 ppm was observed. Moreover, the distinctive magnetism of CQDs @ SLFCO aided in the collection and recycling of the sensor.

The effects of raw materials particle sizes on the solid-state reaction progress, morphology and magnetic properties of M-type strontium hexaferrites

In this work, the effects of SrCO3 and Fe2O3 particle size on the reaction process, morphology and magnetic properties of M-type strontium hexaferrites (SrM) have been further studied. Pure strontium hexaferrite magnetic sample based on SrCO3 and Fe2O3 molar ratio of 1:6 has been successfully prepared at 1150 °C. The results indicated that Fe2O3 particle size was the main factor of affecting the formation of SrM, a pure SrM phase magnetic sample was able to obtain at lower calcination temperatures by using fine Fe2O3 powder as raw material, and at the same calcination temperature, a sample using fine Fe2O3 powder as raw material was able to obtain pure SrM phase magnetic sample with shorter holding time. When the mean particle size of Fe2O3 was below 60 nm, a pure SrM phase magnetic sample was able to form at 1150 °C at a molar ratio of 1:6 of SrCO3 and Fe2O3. In this case, the magnetic parameters of the sample with the optimum magnetic parameters were saturation magnetization MS = 77.8 emu/g and coercive force HC = 4122 Oe. And the solid-state reaction process of the corresponding samples was slightly faster when the mean particle size ratio of Fe2O3 and SrCO3 was between 0.35 and 0.36. Assuming that a SrCO3 particle is surrounded by Fe2O3 particles, it can be inferred that the corresponding molar ratio of Fe and Sr of the nearest raw material particles is between 3.6 and 3.8.

Synthesis and investigation of polyvinylpyrrolidone-polymer content on magnetic and electromagnetic properties of electrospun BiFeO3, SrFe12O19, α-Fe2O3 nanostructures

A one-pot electrospinning technique was employed to synthesize polyvinylpyrrolidone (PVP)-based nanofibers containing bismuth ferrite (BiFeO3), strontium hexaferrite (SrFe12O19), and hematite (α-Fe2O3). The influence of PVP polymer concentration on structural properties revealed the formation of pure phases in all samples, except for BiFeO3 nanofibers, which contained an impurity Bi2Fe4O9 phase. Field-emission scanning electron microscope images showed that higher PVP concentrations resulted in longer, thicker nanofiber chains for all samples. Vibrating sample magnetometer analysis indicated that SrFe12O19 nanofibers exhibited strong ferrimagnetic properties with high saturation magnetization (60 emu g−1) and coercivity (5000 Oe), while the other samples displayed weaker magnetic properties. To address the fragility of nanofibers produced via the one-pot method, the highest PVP concentration nanofibers were incorporated into low and high concentrations of paraffin matrices. Electromagnetic testing showed that paraffin concentration significantly increased the real part of electrical permittivity for BiFeO3 nanofibers (from ∼2 to ∼4.5) compared to other compositions (∼2 to ∼3). Impedance results revealed that BiFeO3 nanofibers had the lowest resistance and likely higher reflectivity. Lastly, the real permittivity of nanofibers decreased with increasing frequency, aligning with Koop’s dielectric relaxation theory.

Study on the structural, magnetic, and magnetodielectric properties of M-type BaFe12O19 and SrFe12O19 hexaferrite nanoparticles

This study addresses the synthesis and characterization of hexagonal barium hexaferrite (BaFe12O19) and strontium hexaferrite (SrFe12O19) nanoparticles, aiming to enhance their structural and magnetic properties for potential applications. Using the sol–gel method, nanoparticles were synthesized and calcinated at 1000 °C, 1100 °C, and 1200 °C for 5 h. A comprehensive analysis was conducted on the prepared nanoparticles' structural, functional, morphological, and magnetic properties. X-ray diffraction confirmed the hexagonal structure and single-crystal phase for BaFe12O19 and SrFe12O19 across all calcination temperatures. The Rietveld analysis of XRD patterns of all the samples have been carried. Fourier transform infrared spectroscopy identified fundamental vibrations at octahedral and tetrahedral sites, verifying the presence of characteristic functional groups. Morphological studies revealed that at an annealing temperature of 1100 °C, the average nanoparticle diameters were 335 nm for BaFe12O19 and 302 nm for SrFe12O19. The elemental analysis and distribution of elements of hexaferrites were studies using Energy Dispersive X-ray Analysis with color mapping method. Magnetic properties were extensively analyzed, including saturation magnetization (Ms), coercivity (Hc), retentivity (Mr), anisotropy field (Ha), squareness ratio (Mr/Ms), and magnetocrystalline anisotropy (K1). At 1100 °C, the magnetic properties of BaFe12O19 are Ms = 55.96 emu/g, Hc = 4308 G, Mr/Ms = 0.51, Ha = 31.30 kG, and K1 = 5.65 × 105 erg/cm3. For SrFe12O19, these values are Ms = 50.80 emu/g, Hc = 3507 G, Mr/Ms = 0.52, Ha = 21.20 kG, and K1 = 5.65 × 105 erg/cm3. Additionally, the study explored the magnetodielectric properties of BaFe12O19 and SrFe12O19 nanoparticles. At a magnetic field of 6000 G, the magnetocapacitance percentage (MC%) and magnetotangent loss percentage (ML%) for BaFe12O19 are −6.23 % and −8.85 %, respectively, while for SrFe12O19, these values are −4.38 % and −1.0 %. The findings indicate that the synthesized hexaferrite BaFe12O19 and SrFe12O19 nanoparticles exhibit significant potential for applications in sensors, permanent magnets, and data recording, with optimized structural and magnetic properties achieved at specific calcination temperatures.

Preparation of strontium hexaferrite based materials by solution combustion: the effect of charges arising in precursors and an external magnetic field

The formation of electric charges during the synthesis of complex oxide materials based on strontium hexaferrite SrFe12O19, including doped with lanthanum and cobalt ions, via the combustion of nitrate-organic precursors has been established. Precursors included polyvinyl alcohol or glycine as organic component. The intensity of charge generation was lower for precursors containing a larger amount of organic component. Data on the magnetic characteristics of the samples were obtained: magnetization, coercive force. The influence of an external magnetic field during the synthesis of hexaferrites significantly affected the coercive force of the samples and allowed to increase its values due to the formation of extended ensembles of nanoparticles. At the same time, such an effect on samples with a relatively low level of charge generation during precursor combustion was more effective. The relationship between the factors influencing the formation of extended aggregates is analyzed. The Sr0.8La0.2Fe11.8Co0.2O19 samples had the maximum coercive force. One of the techniques for increasing the coercive force is a two-stage thermomagnetic treatment, including a low-temperature stage. The formation of branched extended structures at the macro- and micro-levels was found during the combustion of glycine-containing precursors.

Comparative investigation of magneto-fluorescent core@shell nanostructures prepared using hard and soft ferrite as core

The paper focuses on the potential of magneto-fluorescent nanostructures intended to join simultaneously several functions of dissimilar core and shell material into a single entity. Two different types of magneto-fluorescent nanostructures with a broad array of physicochemical properties are premeditated and collated here. Strontium hexaferrite (Hard ferrite) core with CdS shell and Nickel Zinc ferrite (Soft ferrite) core with CdS shell are the two sets of magneto fluorescent nanostructures that were designed. Magnetic and optical analysis of both sets provides divergent outcomes. The shape of the derivative hysteresis curve gives a direct indication of the dissimilar nature (superparamagnetic & Permanent magnetic) of magnetic cores respectively. Optical results depict that both sets of magneto-fluorescent nanostructures are highly stable showing emission only in the position of the CdS shell only.

A comparative study between the physical properties of polyacrylonitrile loaded with 10 wt.% of strontium hexaferrite and those with the same content of nickel cobaltite nanoparticles

A comparative study between the physical properties of polyacrylonitrile loaded with 10 wt.% of strontium hexaferrite and those with the same content of nickel cobaltite nanoparticles

Occupation distribution analysis of Co in La-Co substituted M-type hexaferrite and its significant effect on magnetic properties

In recent years, La-Co co-substituted M-type strontium hexaferrite (La-Co SrM) has gained significant attention due to its improved permanent magnet performance and elevated operating temperature. However, the occupation of Co ions within the lattice of La-Co SrM has sparked considerable debate over the past two decades. To address this, neutron powder diffraction and Raman spectroscopy were employed in this study to analyze Co occupancy in La-Co SrM single crystal and polycrystalline samples. Results consistently reveal a preference for most Co ions to occupy the spin-down tetrahedral 4f1 site, which enhances the net magnetic moment and uniaxial magnetic anisotropy. Differences in Co ion distribution between single crystals (octahedral 12k and 2a sites) and polycrystalline powders (bipyramidal 2b sites) are attributed to sample preparation conditions, often overlooked in previous discussions. Therefore, precise regulation of Co occupancy, particularly maximizing the occupation of the 4f1 site, proves pivotal in enhancing magnetic properties.

Electrochemical hydrogen storage by a new nanocomposite based on tri zinc substituted keggin-type polyoxometalate (PMo9Zn3O37) and strontium hexaferrite (SrFe12O19)

Blending the capabilities of the strontium hexaferrite SrFe12O19 (SRF) with tri zinc substituted Keggin-type polyoxometalate PMo9Zn3O37 (PMZ), to yield PMo9Zn3O37@SrFe12O19 (PMZ@SRF) will have notable ability of hydrogen storage. The use of hydrogen gas as an alternative gas fuel for solving the air pollution has increased its demand by far and need for investigating its storage ways can be clearly observed. Herein, the hypothesis of the ability of novel PMZ@SRF on hydrogen storage was confirmed by chronopotentiometry analysis under a constant current of ±1.5 mA in an electrochemical cell containing of the 6 M of KOH as an electrolyte and the modified cupper foam plate coated with PMZ@SRF nanocomposite as a working electrode. The novel nanocomposite was synthesized by the sol-gel method and characterized by FT-IR, XRD, UV–vis, SEM, EDX, and BET analysis. The characteristic spectra showed the proper synthesis and SEM analysis evaluated the mean size of the nanoparticles 39.44 nm. However, the size of the nanoparticles was calculated by the Debye-Scherrer formula as 29.75 nm with an XRD pattern of the as-prepared PMZ@SRF nanocomposite. Also, BET analysis proved that when PMZ is immobilized on the SRF host the whole new composite will have 0.08 (cm3/g) more pore volume than the raw compound of PMZ. The hydrogen storage capacity will be in priority for thinking new ways of how to have less air pollution, and introducing the significant capabilities of the novel PMZ@SRF on hydrogen storage technology will make a full impact on research areas.

Synthesis of strontium hexaferrite (SrFe12O19) by self-propagating high-temperature synthesis (SHS) method and investigation of the effect of milling on morphology and magnetic properties

In this research, strontium hexaferrite (SrFe12O19) was synthesized using the self-propagating high-temperature synthesis (SHS) method, and its structural and magnetic properties were investigated. Raw materials such as strontium peroxide (SrO2), iron (Fe), and iron (III) oxide (Fe2O3) were used to prepare green compact. The current research investigated the effect of milling time and speed on the morphology and magnetic properties of strontium hexaferrite, and the optimum temperature for calcination was obtained. X-ray diffraction (XRD), vibrating magnetometer (VSM), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM) were used to study the mentioned parameters and choose the optimal conditions for the synthesis of strontium hexaferrite. Milling at speeds of 100, 200, and 300 rpm for 30 and 90 min was investigated. Also, calcination was performed at temperatures of 1000, 1100, 1200, and 1300 °C for 90 min to obtain the optimal temperature. According to the results of VSM analysis, the sample milled at 300 rpm for 90 min and calcined at 1200 °C for 90 min had the highest magnetic properties. Magnetic saturation (MS), magnetic remanence (Mr), and coercivity (HC), with values of 56.43 emu/g, 30.85 emu/g, and 5705.96 Oe, were obtained for this sample. Also, FE-SEM images showing the formation of hexagonal plates with an average particle size of 380 nm after calcination were obtained for the sample with optimal parameters. TEM and HRTEM images also showed the formed particles of strontium hexaferrite with hexagonal morphology.

Effect of rare earth substitution on magnetic properties of strontium hexaferrite prepared by Pechini method

This study presents a comprehensive investigation into the impact of substituting rare earth elements on the magnetic properties of strontium hexaferrite. The samples, synthesized by the sol-gel Pechini method, followed the formula Sr1-xRexFe12O19 with Re = Gd, Sm, Nd, Pr, and La, for 0.025 ≤ x ≤ 0.100. The findings revealed that Re substitution promotes a considerable increment of the coercive field. However, the magnetic yield dropped with increasing the Re content. Therefore, the higher coercivity field, largest magnetization and maximum energy product (BHmax) were reached for samples with x = 0.025. This tendency was consistent across all rare earth-substituted samples although the hexaferrite substituted with samarium and praseodymium showed the strongest hard-magnetic properties. This behavior has been attributed to a reduction of the interaction field due to the emergence of a monodomain structure, and to the limited solubility of rare earth elements within the structure of strontium hexaferrite.

Deciphering the dynamic structural evolution of oxygen vacancies enriched SrFe12O19 for efficient reverse water gas shift reaction

The Reverse Water-Gas Shift (rWGS) reaction is recognized as a potentially promising pathway to serve the dual purpose, possible shifting of CO2 from a linear economy to a circular and positive economic impact in the current industrial process. This study is engaged to develop a series of oxygen vacancies enriched M−type strontium hexaferrite (SrFe12O19) catalysts via doping of transition metals like Cu, Zn, Co, and Ni for the rWGS reaction. Cu-doped SrFe12O19 exhibited 100 % CO selectivity and a CO production rate of 2850 mmol h−1 gcat-1, at a comparatively lower temperature (500 °C), outpacing the performance of almost all non-precious metal-based catalytic systems. Moreover, the catalyst was active without the requirement of the H2 pre-reduction procedure and displayed remarkable stability tested up to 200 h without any significant deactivation, making it more industrially relevant. The characterization of as-prepared catalysts indicates the enrichment of oxygen vacancies and reducibility after the involvement of the dopant in the SrFe12O19 system. The formation of various iron species (Fe3O4, Fe3C, and Fe5C2) was revealed by the in-situ studies and post-reaction characterizations of the catalyst system, and their relative amounts were significantly affected by the nature of doping elements, which subsequently influenced the CO selectivity. The dynamic structural evolution and surface-adsorbedspecies were identified usingin-situ Raman and DRIFTS studies. Finally, the structure–activity relationship was rationalized through not only several ex-situ/in-situ characterization techniques but also an in-detailed Density functional theory (DFT) study.

Aligned Permanent Magnet Made in Seconds–An In Situ Diffraction Study

AbstractThe synthesis of a strontium hexaferrite magnet is studied using in situ synchrotron powder X‐ray diffraction (PXRD) with a 16‐ms time resolution. The precursor material is cold compacted shape‐controlled goethite and strontium carbonate. The time evolution of the phases is modeled with sequential Rietveld refinements revealing that strontium hexaferrite forms within seconds at ≈1173 K. Texture analysis is performed on selected PXRD frames throughout the experiment, and the preferred orientation introduced by cold‐pressing goethite prevails through the iron oxide phase transitions (goethite → hematite → strontium hexaferrite). Electron backscatter diffraction (EBSD) data on the final pellet confirms the preferred orientation observed with PXRD. The resulting magnet has respectable magnetic properties, considering the simplicity of the preparation method, with an energy product (BHmax) of 18.6(8) kJ m−3.