Hans Brouwer
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Hans Brouwer has a total of 43 co-authors. Here are the top co-authors by number of shared publications:
- Marcel J. M. Hermans
Delft University of Technology , Delft, Netherlands
2 shared publications Vera Popovich
2 shared publicationsAlisson Kwiatkowski da Silva
1 shared publication- Amarante J. Böttger
Delft University of Technology
1 shared publication Amir Mohseni Armaki
1 shared publication- Amir Mohseni Armaki
Delft University of Technology
1 shared publication
Latest Publications
- Open Access
- 13 January 2026
- Published by Elsevier in Acta Materialia
- Vol. 306
Double-tough and ultra-strong ceramics: Leveraging multiscale toughening mechanisms through Bayesian optimization
- 13 January 2026
- Published by Elsevier in Acta Materialia
- Vol. 306
Open AccessDouble-tough and ultra-strong ceramics: Leveraging multiscale toughening mechanisms through Bayesian optimization
- Open Access
- 12 November 2025
- Published by Elsevier in Journal of the European Ceramic Society
- Vol. 46 (4)
Oxidation fronts and oxide scale growth modeling in spark plasma sintered ZrC ultra-high temperature ceramic
- 12 November 2025
- Published by Elsevier in Journal of the European Ceramic Society
- Vol. 46 (4)
Open AccessOxidation fronts and oxide scale growth modeling in spark plasma sintered ZrC ultra-high temperature ceramic
- Open Access
- 2 September 2025
- Published by Elsevier in Materials Today
- Vol. 90, 43-51
Unraveling the thermodynamics and mechanism behind the lowering of direct reduction temperatures in oxide mixtures
- 2 September 2025
- Published by Elsevier in Materials Today
- Vol. 90, 43-51
Open AccessUnraveling the thermodynamics and mechanism behind the lowering of direct reduction temperatures in oxide mixtures
- Open Access
- 15 January 2025
- Published by Elsevier in Scripta Materialia
- Vol. 259
Origin of premature fracture and enhancement of superelasticity in laser additively manufactured Ni-rich NiTi metamaterials
- 15 January 2025
- Published by Elsevier in Scripta Materialia
- Vol. 259
Open AccessOrigin of premature fracture and enhancement of superelasticity in laser additively manufactured Ni-rich NiTi metamaterials
- Open Access
Characterisation of Varying Iron Ores and Their Thermal Decomposition Kinetics Under HIsarna Ironmaking Conditions
In the pre-reduction cyclone of the HIsarna process, both thermal decomposition and gas reduction of the injected iron ores occur simultaneously at gas temperatures of 1723–1773 K. In this study, the kinetics of the thermal decomposition of three iron ores (namely OreA, OreB and OreC) for HIsarna ironmaking were analysed as an isolated process with a symmetrical thermogravimetric analyser (TGA) under an inert atmosphere. Using various methods, the chemical and mineralogical composition, particle size distribution, morphology and phase distribution of the ores were analysed. The ores differ in their mineralogy and morphology, where OreA only contains hematite as iron-bearing phase and OreB and OreC include goethite and hematite. To obtain the kinetic parameters in non-isothermal conditions, the Coats–Redfern Integral Method was applied for heating rates of 1, 2 and 5 K/min and a maximum temperature of 1773 K. The TGA results indicate that goethite and hematite decomposition occur as a two-stage process in an inert atmosphere of Ar. The proposed reaction mechanism for the first stage of goethite decomposition is chemical reaction with an activation energy ranging from 46.55 to 60.38 kJ/mol for OreB and from 69.90 to 134.47 kJ/mol for OreC. The proposed reaction mechanism for the second stage of goethite decomposition is diffusion, showing an activation energy ranging between 24.43 and 44.76 kJ/mol for OreB and between 3.32 and 23.29 kJ/mol for OreC. In terms of hematite decomposition, only the first stage was analysed. The proposed reaction mechanism is chemical reaction control. OreA shows an activation energy of 545.47 to 670.50 kJ/mol, OreB one of 587.68 to 831.54 kJ/mol and OreC one of 424.31 to 592.32 kJ/mol.
Open AccessCharacterisation of Varying Iron Ores and Their Thermal Decomposition Kinetics Under HIsarna Ironmaking Conditions
In the pre-reduction cyclone of the HIsarna process, both thermal decomposition and gas reduction of the injected iron ores occur simultaneously at gas temperatures of 1723–1773 K. In this study, the kinetics of the thermal decomposition of three iron ores (namely OreA, OreB and OreC) for HIsarna ironmaking were analysed as an isolated process with a symmetrical thermogravimetric analyser (TGA) under an inert atmosphere. Using various methods, the chemical and mineralogical composition, particle size distribution, morphology and phase distribution of the ores were analysed. The ores differ in their mineralogy and morphology, where OreA only contains hematite as iron-bearing phase and OreB and OreC include goethite and hematite. To obtain the kinetic parameters in non-isothermal conditions, the Coats–Redfern Integral Method was applied for heating rates of 1, 2 and 5 K/min and a maximum temperature of 1773 K. The TGA results indicate that goethite and hematite decomposition occur as a two-stage process in an inert atmosphere of Ar. The proposed reaction mechanism for the first stage of goethite decomposition is chemical reaction with an activation energy ranging from 46.55 to 60.38 kJ/mol for OreB and from 69.90 to 134.47 kJ/mol for OreC. The proposed reaction mechanism for the second stage of goethite decomposition is diffusion, showing an activation energy ranging between 24.43 and 44.76 kJ/mol for OreB and between 3.32 and 23.29 kJ/mol for OreC. In terms of hematite decomposition, only the first stage was analysed. The proposed reaction mechanism is chemical reaction control. OreA shows an activation energy of 545.47 to 670.50 kJ/mol, OreB one of 587.68 to 831.54 kJ/mol and OreC one of 424.31 to 592.32 kJ/mol.
- Open Access
- 29 January 2023
- Published by Springer Nature in High Temperature Corrosion of Materials
- Vol. 99 (3-4) , 201-218
Numerical Model For Short-Time High-Temperature Isothermal Oxidation of Fe–Mn Binaries at High Oxygen Partial Pressure
Since the oxidation reactions in the process of steel production occur in harsh conditions (i.e., high temperatures and gas atmospheres), it is practically impossible to observe in situ the compositional changes in the steel and the formed oxide scale. Hence, a coupled thermodynamic-kinetic numerical model is developed that predicts the formation of oxide phases and the composition profile of the steel alloy’s constituents in a short time due to external oxidation. The model is applied to high-temperature oxidation of Fe–Mn alloys under different conditions. Oxidizing experiments executed with a thermogravimetric analyzer (TGA) on Fe–Mn alloys with different Mn contents (below 10 wt %) are used to determine kinetic parameters that serve as an input for the model. The mass gain data as a function of time show both linear and parabolic regimes. The results of the numerical simulations are presented. The effect of different parameters, such as temperature, Mn content of the alloy, oxygen partial pressure, and oxidizing gas flow rate on the alloy composition and oxide phases formed, is determined. It is shown that increasing the temperature and decreasing the oxygen partial pressure both lead to a thicker depleted area.
- 29 January 2023
- Published by Springer Nature in High Temperature Corrosion of Materials
- Vol. 99 (3-4) , 201-218
Open AccessNumerical Model For Short-Time High-Temperature Isothermal Oxidation of Fe–Mn Binaries at High Oxygen Partial Pressure
Since the oxidation reactions in the process of steel production occur in harsh conditions (i.e., high temperatures and gas atmospheres), it is practically impossible to observe in situ the compositional changes in the steel and the formed oxide scale. Hence, a coupled thermodynamic-kinetic numerical model is developed that predicts the formation of oxide phases and the composition profile of the steel alloy’s constituents in a short time due to external oxidation. The model is applied to high-temperature oxidation of Fe–Mn alloys under different conditions. Oxidizing experiments executed with a thermogravimetric analyzer (TGA) on Fe–Mn alloys with different Mn contents (below 10 wt %) are used to determine kinetic parameters that serve as an input for the model. The mass gain data as a function of time show both linear and parabolic regimes. The results of the numerical simulations are presented. The effect of different parameters, such as temperature, Mn content of the alloy, oxygen partial pressure, and oxidizing gas flow rate on the alloy composition and oxide phases formed, is determined. It is shown that increasing the temperature and decreasing the oxygen partial pressure both lead to a thicker depleted area.
- Open Access
Controlling the Oxygen Defects Concentration in a Pure BiFeO3 Bulk Ceramic
BiFeO3 is a multiferroic material with a perovskite structure that has a lot of potential for use in sensors and transducers. However, obtaining pure single-phase BiFeO3 ceramic with a low electrical conductivity via solid-state reactions remains a problem that limits its application. In this work, the suppression of secondary phases in BiFeO3 was studied by varying the compositional parameters and the sintering temperature. The addition of 1% Bi2O3 to the stoichiometric precursor mixture prevented the formation of secondary phases observed when sintering stoichiometric precursors. The pure phase ceramic had a p-type conductivity and a three-decade lower electrical conductivity as measured by impedance spectroscopy. Annealing of optimally synthesized material at different partial pressures of oxygen in an oxygen–nitrogen gas atmosphere showed that the reason for this type of conductivity lies in the high concentration of defects associated with oxygen. By annealing in various mixtures of nitrogen and oxygen, it is possible to control the concentration of these defects and hence the conductivity, which can go down another two decades. At a pO2 the conductivity is determined by intrinsic charge carriers in the material itself.Open AccessControlling the Oxygen Defects Concentration in a Pure BiFeO3 Bulk Ceramic
BiFeO3 is a multiferroic material with a perovskite structure that has a lot of potential for use in sensors and transducers. However, obtaining pure single-phase BiFeO3 ceramic with a low electrical conductivity via solid-state reactions remains a problem that limits its application. In this work, the suppression of secondary phases in BiFeO3 was studied by varying the compositional parameters and the sintering temperature. The addition of 1% Bi2O3 to the stoichiometric precursor mixture prevented the formation of secondary phases observed when sintering stoichiometric precursors. The pure phase ceramic had a p-type conductivity and a three-decade lower electrical conductivity as measured by impedance spectroscopy. Annealing of optimally synthesized material at different partial pressures of oxygen in an oxygen–nitrogen gas atmosphere showed that the reason for this type of conductivity lies in the high concentration of defects associated with oxygen. By annealing in various mixtures of nitrogen and oxygen, it is possible to control the concentration of these defects and hence the conductivity, which can go down another two decades. At a pO2 the conductivity is determined by intrinsic charge carriers in the material itself. - Open Access
Applicability Study of Pulsed Laser Beam Welding on Ferritic–Martensitic ODS Eurofer Steel
Pulsed laser beam welding was used successfully to join the oxide dispersion-strengthened (ODS) Eurofer steel. The joining was conducted with a laser power of 2500 W and a pulsed duration of 4 ms. With the filler material being used, a minor material loss and microvoids were observed in the joint. The microstructure of the fusion zone consists of dual phase elongated structures. The heat-affected zone has a width of around 0.06 mm with finer grains. The transmission electron microscopy observation reveals that nanoprecipitates are finely distributed in the fusion zone. The tensile strength, yield strength and elongation of the joint are slightly inferior to the base material. The fractography results reveal a typical ductile fracture. The experimental results indicate a reasonable joint from the perspective of both the microstructure and mechanical behaviour.
Open AccessApplicability Study of Pulsed Laser Beam Welding on Ferritic–Martensitic ODS Eurofer Steel
Pulsed laser beam welding was used successfully to join the oxide dispersion-strengthened (ODS) Eurofer steel. The joining was conducted with a laser power of 2500 W and a pulsed duration of 4 ms. With the filler material being used, a minor material loss and microvoids were observed in the joint. The microstructure of the fusion zone consists of dual phase elongated structures. The heat-affected zone has a width of around 0.06 mm with finer grains. The transmission electron microscopy observation reveals that nanoprecipitates are finely distributed in the fusion zone. The tensile strength, yield strength and elongation of the joint are slightly inferior to the base material. The fractography results reveal a typical ductile fracture. The experimental results indicate a reasonable joint from the perspective of both the microstructure and mechanical behaviour.