3.2. Evolution of Microstructure of Heat Treated Samples
The evolution of the microstructure in the experimental samples, subjected to varying rolling reductions followed by annealing at three different temperatures, is presented in
Figure 3. Metallographic cross-sections were examined using light optical microscopy, with the longitudinal section oriented parallel to the rolling direction. The results show that the samples exhibit a ferritic microstructure with grain size and morphology strongly dependent on the applied processing conditions. The variation in the average grain size with deformation and annealing temperature is shown graphically in
Figure 4.
For samples with a temper rolling reduction of ~2%, microstructural changes were highly sensitive to annealing temperature. At 850 °C (
Figure 3a1), the microstructure closely resembled that of the initial sample (
Figure 2a), with an average grain size of 43.5 ± 3.6 µm, indicating only minor growth. Annealing at 900 °C (
Figure 3a2) produced an inhomogeneous grain size distribution (average 73.3 ± 5.2 µm), with two distinct regions: coarse grains of 150–250 µm occupying over 50% of the cross-section, and smaller primary recrystallized grains scattered between them. At 950 °C (
Figure 3a3), a nearly homogeneous coarse-grained microstructure formed, with grains of similar size and shape uniformly distributed across the section. Image analysis gave an average grain size of 199 ± 10 µm. These observations show that even minimal deformation can strongly influence microstructural evolution during higher-temperature annealing, with increasing temperature developing coarser, more uniform grains, desirable for soft magnetic FeSi alloys.
The microstructures of samples subjected to 4% deformation and annealed at the three selected temperatures are shown in
Figure 3b1–b3. All exhibit secondary recrystallized microstructures with approximately uniform grain distribution morphology across the cross-section, but with notable differences in average grain size. The smallest grains (137.4 ± 7 µm) were obtained after annealing at 850 °C, while the largest (379.3 ± 15 µm) formed at 950 °C. The sample annealed at 900 °C (
Figure 3b2) showed an average grain size of 154.6 ± 5 µm, only slightly larger than at 850 °C; however, several grains exceeded the mean size by several times, indicating mild inhomogeneity in the secondary recrystallization process. The 950 °C sample (
Figure 3b3) displayed exceptionally large grains, many with a columnar morphology, suggesting that their growth during dynamic recrystallization annealing likely initiated at the sheet surface.
The optical analysis results for samples subjected to 6% temper rolling deformation followed by heat treatment are presented in
Figure 3c1–c3. Morphological analysis of these microstructures reveals no significant differences among them. The observed light-optical microstructures generally display a uniform grain distribution without notable variations in grain size. At first glance, it is evident that increasing the annealing temperature leads to a slight increase in the average grain size—a trend also reflected in the graph shown in
Figure 4. Image analysis confirms that the average grain sizes for the samples (ε~6%) annealed at 850 °C, 900 °C, and 950 °C are approximately 115.2 ± 6 µm, 120.4 ± 7 µm, and 153.9 ± 11 µm, respectively.
The effect of dynamic annealing on the microstructure of samples with 8% temper rolling deformation is shown in
Figure 3d1–d3. In all cases, annealing at 850 °C, 900 °C, and 950 °C, the grain size and shape distributions remain similar. Image analysis determined average grain sizes of 97.8 ± 6 µm, 110.5 ± 7 µm, and 118.2 ± 11 µm, respectively, indicating that increasing the annealing temperature has only a limited effect on grain growth at this deformation level. Comparable behaviour was observed in samples subjected to a 10% thickness reduction (
Figure 3e1–e3), where annealing temperature had a negligible influence on grain size, which ranged from approximately 86 µm to 100 µm (
Figure 4).
The smallest average grain size, approximately 70 ± 5 µm, was recorded in samples deformed by 40% (
Figure 3f1–f3). After annealing at 850 °C, 900 °C, and 950 °C, these samples exhibited pronounced homogeneity, with fine, equiaxed grains uniformly distributed throughout the sheet cross-section.
The evolution of average grain size as a function of deformation and annealing temperature is summarised in
Figure 4. The results clearly demonstrate that small deformations (the optimal deformation in our work is 4%) combined with high-temperature dynamic annealing can produce exceptionally large grains, significantly exceeding those of the initial industrial microstructure. In contrast, higher deformation levels (≥8%) suppress grain growth, yielding finer and more uniform microstructures, regardless of the annealing temperature. This confirms that the proposed unconventional processing route, temper rolling with small deformation followed by rapid dynamic annealing, can be effectively tuned to achieve targeted grain sizes and morphologies in fully finished electrical steel, which is additionally heat-treated by electrical equipment manufacturers after cutting segments for rotors and stators.
3.3. Analysis of Cold-Rolled Deformed States
This part of the scientific work was related to the analysis of plastic mechanical strains generated through the cross-section of sheet thickness during the temper rolling processes. In the case of primary recrystallization, the strain-induced boundary migration plays a key role in the occurrence of coarse-grained microstructures with a desirable crystallographic orientation [
27]. Because of this reason, it is very important to know how the mechanical strain is distributed within the observed microstructural matrix subjected to external mechanical deformation. It is well known that in the last decades, the EBSD method began to be widely used for the detection of plastic strains in metallic materials with polycrystalline structures in the scientific practice. As dislocation is created in the material structure under mechanical work, the residual strain is manifest as local degradation in lattice structures by weak deviation in their orientation [
49]. EBSD measurements enable the acquisition of extensive crystallographic data from individual points within the scanned area and allow for the generation of Kernel Average Misorientation maps on the background of the investigated microstructure. These maps are constructed by estimating the average misorientation angle of the crystal lattice between neighbouring pairs of points on the measurement grid, thereby providing insights into the distribution of local plastic strain and dislocation density within the material.
One-to-one EBSD measurements were performed to characterise the distribution of mechanical strains associated with applied plastic deformations, which contribute to the most effective abnormal selective grain growth during subsequent heat treatment. The KAM maps illustrating (comparing) the distribution of residual strains across the cross-section of experimental samples subjected to varying degrees of deformation are presented in
Figure 5. The microstructural matrices of the deformed samples, corresponding to deformation levels ranging from 2% to 40%, are displayed on the left side of the figure. The rainbow-colored regions within the analysed microstructures reflect the intensity of local misorientation angles, which are indicative of dislocation density. On the right side of the figure, the corresponding frequency distributions of misorientation angles are shown, using a colour palette ranging from blue to red along the KAM value axis. These graphical representations are consistent with the colour schemes used in the respective KAM maps. In this context, the light blue regions indicate areas of the crystal lattice with minimal distortion, while red regions correspond to zones with the highest levels of local misorientation (about 5°), representing regions of elevated plastic strain and dislocation density.
The distribution of local misorientation angles across the thickness of samples subjected to approximately 2% deformation is presented in
Figure 5a1,a2. The coloured KAM map (
Figure 5a1) depicts the fully recrystallized matrix of the experimental steel, showing slight variations in colour corresponding to regions of crystal lattice distortion. The EBSD data were processed to generate a graph of the relative frequency of local misorientation as a function of misorientation angle, shown in
Figure 5a2. The results indicate that, for the 2% deformed sample, misorientation angles range from 0° to 2.5°, with the most frequent angle being approximately 0.8°. This low level of misorientation reflects minimal plastic strain within the crystal lattice. The coloured KAM maps reveal that these strain-related misorientations are predominantly located near grain boundaries, where the angles reach approximately 2–2.5°. In contrast, the interior regions of the grains show either no misorientation or only weak misorientations ranging from 0.5° to 1.5°. A comparison of
Figure 5a1,a2 confirms that lattice distortions caused by rolling are unevenly distributed throughout the microstructure, being primarily concentrated at grain boundaries.
The EBSD data presented in the form of a KAM map for the sample subjected to 4% temper rolling reduction are shown in
Figure 5b1,b2. Compared to the 2% deformed sample, the distribution of local misorientation angles exhibits notable differences. The graph in
Figure 5b2 shows that misorientation angles extend up to approximately 3°, with the highest relative frequency observed at around 0.9°. The KAM map indicates that plastic strain is still predominantly concentrated near the grain boundaries. Remarkably, a pronounced colour gradient is observed within some grains, ranging from light blue to light yellow. This gradient likely corresponds to a decreasing dislocation density from the grain boundary toward the grain centre. Additionally, a small number of grain boundaries show colour transitions from yellow to light red, corresponding to local misorientation angles of approximately 3.5–4.0°. From a microstructural perspective, the misorientation distribution reveals a non-uniform morphology. Overall, the EBSD analysis of the 4% deformed sample suggests that the increased deformation results in more pronounced local mechanical strain within the crystal lattice, particularly at grain boundaries, with an observable gradient of strain extending into the grain interiors.
The microstructure exhibiting local mechanical strains, obtained after temper rolling the experimental sample with a 6% thickness reduction, along with the corresponding distribution of local misorientation angle intensity, is shown in
Figure 5c1,c2, respectively. The KAM map clearly reveals an inhomogeneous distribution of local plastic strains throughout the sample thickness. Certain grains exhibit higher local misorientation values than others. However, the colour distribution within individual strained grains appears relatively uniform, without significant gradients. The observed range of misorientation angles extends from approximately 0.2° to 3.4°. Compared to previous results, the peak of the relative frequency curve is shifted to a higher value, with a maximum at approximately 1.1°, as shown in
Figure 5c2. These results suggest that in the 6% deformed sample, although the intra-grain strain gradient is less distinct, there is a noticeable increase in the overall intensity of local misorientation. This implies an accumulation of stored deformation energy in the microstructure as a result of the rolling process.
The behaviour of misorientation angles in the experimental sample subjected to 8% thickness reduction by temper rolling is illustrated in
Figure 5d1,d2. The EBSD data clearly indicate that increasing the degree of deformation results in higher intensities of local misorientation at greater angles. The KAM curve is shifted to the right, with most values falling within the range of 0.5° to 3.5°, and a maximum frequency occurring at approximately 1.2°. The most informative insight is provided by the coloured KAM map in
Figure 5d1. It shows that increased local misorientation angles are visually represented by a greater number of regions coloured in orange and light red, primarily located near grain boundaries and unevenly distributed throughout the microstructure. Significantly, the microstructure contains grains exhibiting a pronounced gradient of local misorientation, which generally increases toward the grain boundaries.
The EBSD analysis of the sample subjected to a 10% deformation is presented in
Figure 5e1,e2. The results show that the misorientation angles increase up to approximately 4°, with the lowest visible value around 0.4°, as seen in
Figure 5e2. This suggests that greater deformation develops the range of misorientation angles, indicating an increase in stored energy within the crystal lattice. The KAM map in
Figure 5e1 presents that this increase in local lattice distortion is most pronounced in the central part of the microstructure, particularly near grain boundaries. In this deformation state, gradients of misorientation are detectable not only within individual grains but also across the thickness of the sample. The map further demonstrates that the highest misorientation intensities are concentrated predominantly in the middle region of the microstructure.
The microstructure of the rolled samples subjected to 40% deformation is presented in
Figure 5f1,f2. The coloured KAM map clearly shows that the metallographic structure is characterised by elongated grains aligned along the rolling direction. The EBSD data indicate that such a high level of deformation significantly modifies the original grain morphology within the primary microstructural matrix. The observed grain elongation suggests that the crystal lattice has undergone extensive strain due to intense shear stresses. This deformation is visualised by the colouration on the KAM map, which reflects the values of local misorientation angles. The KAM graph in
Figure 5f2 shows that local misorientation angles range from 1° to 5°, with the peak intensity occurring around 2.5°. The processed data reveal a relatively high frequency of misorientation angles between 4° and 5°, which are predominantly located along the boundaries of the elongated grains (orange and red areas). This indicates that, under 40% plastic deformation, dislocations are primarily generated and stored near grain boundaries. As a result, the subsequent heat treatment of this sample most likely led to a recovery process, manifested as primary recrystallization, rather than secondary recrystallization, which was observed in samples deformed by 2–10%. This interpretation is further supported by the differences in microstructural states illustrated in
Figure 5.
The EBSD-based KAM analysis demonstrates a clear correlation between temper rolling deformation and the evolution of local plastic strains in FeSi steel. At low deformation levels (2–4%), misorientation angles are small and primarily concentrated at grain boundaries, indicating limited strain accumulation and minimal lattice distortion. As deformation increases (6–10%), both the magnitude and distribution of misorientations grow, reflecting higher dislocation density and more pronounced strain gradients extending into grain interiors. At extreme deformation (40%), extensive grain elongation and elevated misorientation values highlight significant strain localisation near boundaries as well as throughout the thickness of the sample, suggesting that dislocation storage and lattice distortion are maximised.
These observations indicate that temper rolling not only increases the overall stored deformation energy but also alters the heterogeneity of strain distribution, which is a critical factor governing subsequent recrystallization behaviour. In particular, low to moderate deformations favour abnormal selective grain growth during secondary recrystallization, whereas high deformation promotes recovery and primary recrystallization due to excessive strain accumulation and grain elongation. Overall, the presented analysis provides valuable insights into the distribution and intensity of local plastic strains induced by temper rolling over a wide range of applied deformations in FeSi steel samples. The KAM maps, together with the corresponding misorientation frequency distributions, clearly demonstrate how increasing deformation influences dislocation density, strain localisation, and grain boundary behaviour, factors that play a decisive role in recrystallization mechanisms and the resulting microstructural characteristics
3.4. Analysis of Texture Components of Heat-Treated Samples
In industrial production, the isotropic magnetic properties of non-oriented FeSi steels are ideally ensured by the formation of a completely random crystallographic texture. However, the directional nature of hot and cold rolling processes inevitably introduces a certain degree of crystallographic anisotropy, whether intended or not. A fully random texture may not even be optimal for rotating electrical machines such as motors or generators. What is essential is that the material exhibits good and uniform magnetic properties when magnetised in any in-plane direction of the steel sheet. Optimal magnetic performance is typically achieved by minimising the presence of <111> crystallographic orientations in the sheet plane and enhancing the intensity of <100> orientations. Although achieving both simultaneously is technically challenging, it is nevertheless possible to significantly improve the magnetic properties of NO FeSi steels through precise control over the processing steps.
EBSD data, presented in the form of IPF maps and ODF sections, are shown in
Figure 6. These colour-coded maps allow for a fast and accurate visualisation of the crystallographic texture of the analysed samples.
From a representation standpoint, IPF maps are particularly useful for polycrystalline materials, as they provide information on the morphology of the microstructural matrix, including grain size and crystallographic orientation across the scanned surface. Each coloured grain in the IPF map corresponds to a specific crystallographic direction straight with a defined reference direction—typically the rolling direction in textured FeSi steels. This orientation-specific colouring facilitates quick interpretation and understanding of the material’s preferred orientation (texture) in the observation plane. It is important to note that, in IPF maps, three primary colours are most significant: red, green, and blue, which correspond to the {100}, {110}, and {111} crystallographic planes, respectively.
The orientation distribution function is a two-dimensional function specified by at least three Euler angles which provides a quantitative method for evaluating the crystallographic texture of polycrystalline materials. It describes the statistical distribution of grain orientations within the sample. In ODF representations, each orientation is expressed as the volume fraction (or percentage) of grains that adopt a specific crystallographic alignment. In other words, the ODF enables the precise assessment of the intensity of particular crystallographic orientations, complementing the qualitative information provided by the coloured IPF maps.
The evolution of crystallographic texture in selected experimental microstructural states, obtained from temper-rolled samples heat-treated at 950 °C, is presented in
Figure 6. The processed EBSD data indicate that the applied dynamic thermal processing of slightly rolled FeSi steels influences not only the development of the microstructural matrix but also promotes selective grain growth, particularly enhancing the intensity of desirable crystallographic components such as the cubic {100}<001> and Goss {110}<001> orientations.
The crystallographic texture of the samples subjected to 2% deformation followed by heat treatment is presented in
Figure 6a1. The IPF map reveals that the material exhibits a relatively coarse-grained microstructure, with the predominant crystallographic directions <100> and <110> aligned parallel to the sheet rolling direction, indicated by different shades of red and green. In terms of the intensity of specific crystallographic orientations within the observed microstructural matrix, additional insight is provided by the ODF sections, which show increased intensities of the α- and θ-fibre components (see
Figure 6a2). The highest intensity is associated with the {113}<361> component, corresponding to a slightly rotated cube orientation at Φ = 15°. Another notable intensity maximums are related to the {100}<013> cube component and indistinctness Goss orientation.
The IPF-coloured map illustrating the main crystallographic components identified in the samples subjected to 4% cold rolling followed by heat treatment is shown in
Figure 6b1. The results indicate that most of the coarsened grains appear in red or reddish shades, signifying crystallographic orientations close to the rotated cube texture. A more detailed analysis based on the θ-fibre section of the ODF (
Figure 6b2) reveals that these grains exhibit a rotated cube texture, with the <013> family of directions aligned parallel to the RD. In other words, the crystallographic lattice of these grains lies within the {100} plane and is rotated by approximately 15° with respect to the cold rolling direction of the examined sample.
The evolution of texture in the samples subjected to 6% cold rolling and subsequently heat-treated under dynamic conditions at 950 °C is presented in
Figure 6c1,c2. The IPF map (
Figure 6c1) shows that the coarser components of the microstructural matrix are predominantly associated with rotated cube and deviated Goss orientations. In contrast, finer constituents (grains) mainly display the undesirable deformed texture, represented by the γ-fibre in the ODF section. The two-dimensional ODF representation in
Figure 6c2 further indicates that many of the texture components of the microstructure are rotated by several degrees from the cube orientation {100}<110>. Additionally, in this microstructure, a distinctly visible region of high texture intensity corresponds to a double-oriented cube component {100}<110>, located central part of the θ-fibre. Also, features associated with the deformed texture, along with their characteristic orientations, are concentrated near the γ-fibre.
Figure 6d1,d2,e1,e2 show the crystallographic textures of the samples subjected to 8% and 10% cold rolling, respectively. The IPF maps (
Figure 6d1,e1) confirm earlier observations, indicating that both samples exhibit a homogeneous microstructural matrix without distinctly pronounced texture components. This is further supported by the ODF sections (
Figure 6d2,e2). As evident from these results, the samples do not display a dominant texture component but rather exhibit a balanced distribution of crystallographic planes and directions. These are situated near or between the principal textural components associated with the θ-, γ-, and α-fibres, as illustrated in the coloured ODF sections.
Analyses of EBSD data for the samples subjected to a maximum cold rolling reduction of approximately 40% followed by heat treatment, are presented in
Figure 6f1,f2. The IPF map presents a fine-grained microstructure dominated by grains with {100} and {110} crystallographic planes, corresponding to the strong {100}<0vw> and {110}<0vw> components, respectively. The microstructure is predominantly shaded in red and green, which represent the Goss orientation and the θ-fibre, as confirmed by the coloured ODF section in
Figure 6f2.
Overall, the evolution of crystallographic texture with increasing deformation reveals a clear the principles of formation of crystallographic grain orientation in the process of secondary recrystallization in the investigated FeSi samples. At lower deformation levels (2–4%), the texture is dominated by rotated cube or Goss components. This behaviour of resulting texture can be attributed to the fact that, during primary recrystallization, a slight plastic strain gradient between adjacent grains or inside of grain (see
Figure 5a1,a2,b1,b2, combined with a pronounced temperature gradient across the sheet thickness, promotes the preferential growth of grains with crystallographic orientations located near the θ-fibre in the primary recrystallized state. However, with increasing cold rolling degree to 6%, more numerous textural components develop with the coexistence of cubic, deviation Goss and deformed crystallographic components. Considering the results obtained for these samples from EBSD data in the form of KAM maps (see
Figure 5c1,c2), it is evident that with applied deformation starting from 6%, the morphology of the occurrence of local mechanical stresses in the crystal lattice changes. Comparison of the results shown in KAM maps for samples with 2–4% deformation and samples with 6% deformation indicates that with increasing deformation above 4%, the weak gradients of plastic mechanical stresses are replaced by a gradient that is more pronounced throughout the thickness of the sheet than between individual structures of the observed microstructural matrix. Such a distribution of dislocation densities in the deformed crystal lattice during secondary recrystallization at extremely high heating rates provides more grains of the primary recrystallized matrix with the accumulated deformation energy necessary to activate the motion of their boundaries. As a result, the sample with 6% deformation has a finer-grained microstructure with a larger number of different crystallographic components than in samples with lower applied deformation. With further deformation (8–10%), the texture becomes more dispersed and homogenised, reflecting a balance between deformation and recrystallization mechanisms. At the highest deformation level (40%), the resulting microstructure is characterised by a fine-grained morphology, with an average grain diameter of approximately 70 μm. As shown in
Figure 6f2, a broad spectrum of crystallographic orientations is present within the observed microstructure, without a dominant or preferential textural component. Taking into account the results of metallographic analysis (
Figure 3f1,f2) and the detection of local mechanical stresses within the primarily recrystallized matrix of the 40% deformed sample, it can be assumed that deformation levels exceeding 10% do not promote the selective growth of ferrite grains with preferred cube or Goss orientations.
Based on the presented findings, it can be concluded that the mechanism of selective strain-induced boundary migration of ferrite grains is effectively activated only when the cold rolling reduction does not exceed 10%. This effect occurs in combination with subsequent rapid heating, which generates a significant temperature gradient between the surface and core of the heat-treated thin FeSi steel sheets.
3.5. Analysis of Magnetic Properties of Experimental Samples
Among the wide range of steel materials produced today, electrical silicon steels are particularly distinguished by their electromagnetic properties, as they are used primarily for transmitting induced magnetic fields in the cores of electrical devices. Accordingly, the design of microstructural, textural, and substructural parameters, as well as the chemical composition, must ultimately have a positive influence on their final magnetic properties. These properties are most commonly evaluated by measuring coercivity or power losses. In this context, our research focused on improving the microstructural and textural characteristics of the investigated steels in the “fully finished” state, with the expectation that the measured magnetic parameters of the processed samples would correspond to the results presented and discussed in the preceding chapters.
The evolution of microstructural, substructural, and textural characteristics in the investigated steel states has a direct impact on their final magnetic properties, namely coercivity and power losses. Magnetic measurements were performed on all experimental samples in an AC magnetic field at a frequency of 50 Hz. The dependence of coercivity on the material state of the experimental samples is presented in
Figure 7. The resulting curves show that coercivity varies with both annealing temperature and applied deformation, indicating that the samples differ not only in microstructure, texture, and the intensity of crystal lattice disruption caused by rolling, but also in their corresponding magnetic properties.
The initial coercivity of the as-delivered samples is approximately 162 A/m. The graph illustrates that, among the measured samples, those corresponding to the final state of the M530-50A grade exhibit the highest coercivity and, consequently, the greatest power losses, compared with other material states in which selective development of the microstructural matrix with larger grains and a preferred crystallographic texture was applied. The minimum coercivity of approximately 65 A/m was achieved in a sample subjected to mild smooth rolling (~4% thickness reduction) followed by dynamic annealing at 950 °C. These results indicate that, for this FeSi steel grade, combining ~4% deformation with subsequent heat treatment at 950 °C under an extremely high heating rate can reduce coercivity by more than a factor of two relative to the as-delivered state. The measured coercivity values for this condition correspond closely with the microstructure and texture analyses performed on the same sample.
It is also noteworthy that samples rolled at above or below 4% deformation exhibited a positive improvement in their magnetic properties compared to the as-delivered sheets. Clearly, increasing the average grain size or enhancing the textural parameters of the microstructural matrix has a beneficial effect on reducing magnetic losses in electrical steels. To a certain extent, the coercivity measurements presented in
Figure 7 can be considered a linear reflection of the average grain size values shown in
Figure 4.
In conclusion, it can be stated that the results of this study demonstrate a clear relationship between temper rolling deformation, heat treatment, microstructural evolution, texture development, and the magnetic properties of FeSi steels. EBSD analysis revealed that increasing rolling reductions progressively enhances local plastic strain and dislocation density, particularly near grain boundaries, as indicated by KAM maps. At low deformation levels (2–4%), strains are localised primarily at grain boundaries, with minimal intra-grain gradients, which are nevertheless sufficient to promote significant selective grain growth via the strain-induced grain boundary migration mechanism during secondary recrystallization. Conversely, higher deformations (8–40%) induce pronounced lattice distortions and strain gradients extending into grain interiors, accompanied by significant grain elongation along the rolling direction. It is evident that at higher deformation levels, not only does the intensity of mechanical stresses within the crystal lattice increase, but their overall occurrence throughout the deformed structure also becomes more widespread. Consequently, the deformation gradient between different regions of the microstructural matrix, particularly between adjacent grains, becomes less pronounced. During subsequent heat treatment, this reduced gradient allows a much larger number of grains to grow simultaneously compared to lower deformation levels (below 4%), where selective growth is more prevalent. As these grains compete and inhibit one another’s growth, the resulting microstructure becomes more or less homogeneous, accompanied by a reduction in the average grain diameter.
These microstructural changes directly influence recrystallization behaviour and the development of preferred crystallographic textures, which in turn affect magnetic performance. Coercivity measurements show that moderate rolling reductions combined with dynamic annealing (e.g., 4% deformation at 950 °C) lead to a substantial decrease in coercivity and power losses, consistent with the formation of coarser, more uniform grains with favourable orientations. Conversely, higher deformations, while increasing stored strain energy, promote fine-grain structures and heterogeneous distributions of their crystallographic orientations, resulting in comparatively higher coercivity. Overall, the findings highlight that precise control of mechanical deformation and subsequent heat treatment enables optimisation of microstructure and texture, thereby minimising coercivity and enhancing the electromagnetic performance of fully finished FeSi steels. This establishes a direct link between mechanical processing, internal lattice strains, and functional magnetic properties.