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Publikasjoner (10 av 86) Visa alla publikasjoner
Hanif, I. & Wiinikka, H. (2026). Calcination of CaCO3 and the subsequent sintering/densification of CaO directly visualized with in-situ SEM. Materials Chemistry and Physics, 356, Article ID 132296.
Åpne denne publikasjonen i ny fane eller vindu >>Calcination of CaCO3 and the subsequent sintering/densification of CaO directly visualized with in-situ SEM
2026 (engelsk)Inngår i: Materials Chemistry and Physics, ISSN 0254-0584, E-ISSN 1879-3312, Vol. 356, artikkel-id 132296Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

This work investigates the possibility and potential insights gained from in-situ scanning electron microscopy (SEM) experiments focused on the dynamic heating of CaCO3 for calcination processes. MEMS chips were used to facilitate uniform heating, precise control of heating parameters and reproducibility, providing a controlled environment for comprehensive experimentation. This work focuses on the microstructure transformation, with particular emphasis on the meso- and macropores, grain formation, and the sintering behavior of these particles. Influence of heating rates and complex interplay of temperature and microstructural transformations was revealed. The results obtained may be useful for optimization and microstructural-based design of the calcination procedures for complex process engineering in various applications.

sted, utgiver, år, opplag, sider
Elsevier Ltd, 2026
Emneord
In-situ SEM, MEMS heating, Meso- and macropores, Grain formation, Calcination, Sintering
HSV kategori
Forskningsprogram
Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-116747 (URN)10.1016/j.matchemphys.2026.132296 (DOI)001711194400001 ()2-s2.0-105031967398 (Scopus ID)
Merknad

Full text: CC BY license;

For funding information, see: https://doi.org/10.1016/j.matchemphys.2026.132296

Tilgjengelig fra: 2026-03-16 Laget: 2026-03-16 Sist oppdatert: 2026-04-07
Ivanoff, A., Sepman, A., Granlund, A., Wiinikka, H. & Westerberg, L.-G. (2026). In situ TDLAS diagnostics of nitric oxide in combustion and plasma heated gases. Applied Optics, 65(18), 6050-6059
Åpne denne publikasjonen i ny fane eller vindu >>In situ TDLAS diagnostics of nitric oxide in combustion and plasma heated gases
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2026 (engelsk)Inngår i: Applied Optics, ISSN 1559-128X, E-ISSN 2155-3165, Vol. 65, nr 18, s. 6050-6059Artikkel i tidsskrift (Fagfellevurdert) Published
sted, utgiver, år, opplag, sider
Optica Publishing Group, 2026
HSV kategori
Forskningsprogram
Strömningslära; Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-118256 (URN)10.1364/ao.599175 (DOI)
Forskningsfinansiär
Swedish Energy Agency, (P2022-00908, P2024-03006)Bio4Energy
Tilgjengelig fra: 2026-06-12 Laget: 2026-06-12 Sist oppdatert: 2026-06-12bibliografisk kontrollert
Wiinikka, H., Vikström, T., Sepman, A., Nilsson Pingel, T., Weiland, F. & Wennebro, J. (2026). Non-catalytic methane pyrolysis: Influence of reactor temperature on the yields of hydrogen, acetylene, and carbon nanoparticles and its turbostratic structure. International journal of hydrogen energy, 247, Article ID 155872.
Åpne denne publikasjonen i ny fane eller vindu >>Non-catalytic methane pyrolysis: Influence of reactor temperature on the yields of hydrogen, acetylene, and carbon nanoparticles and its turbostratic structure
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2026 (engelsk)Inngår i: International journal of hydrogen energy, ISSN 0360-3199, E-ISSN 1879-3487, Vol. 247, artikkel-id 155872Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Methane pyrolysis (MP), where CH4 is thermally decomposed to H2 and solid carbon is a CO2 free H2 production technique. By performing non-catalytic MP experiments in the temperature range of 1100°C-1700 °C we showed that the produced carbon nanoparticles (CNP) have a similar elemental composition (C, H, O, and N) and turbostratic nanostructure compared to rubber grade carbon black (CB) if the reactor temperature is ∼1400 °C with 100% conversion of the CH4 to CNP, C2H2, and H2 with product yields of ∼0.53 g/gfuel, ∼0.23 g/gfuel, and ∼0.24 g/gfuel, respectively. By increasing the reactor temperature above 1400 °C, further decomposition of the C2H2 to CNP and H2 occurs, and the theoretical yield of 0.75 g/gfuel of CNP and 0.25 g/gfuel H2 could be reached. However, the turbostratic nanostructure of the CNP at higher temperatures was too graphitized compared to rubber grade CB and instead more like electro conductive CB.

sted, utgiver, år, opplag, sider
Elsevier Ltd, 2026
Emneord
Methane pyrolysis, Hydrogen, Carbon black, Turbostratic carbon, TEM
HSV kategori
Forskningsprogram
Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-118335 (URN)10.1016/j.ijhydene.2026.155872 (DOI)2-s2.0-105040696954 (Scopus ID)
Forskningsfinansiär
Swedish Research Council Formas, 2020-01992Swedish Research Council, 2020-04453The Kempe Foundations, SMK-1641.2Bio4Energy
Merknad

Full text license: CC BY 4.0;

Funder: Energy Technology Center in Piteå, Sweden

Tilgjengelig fra: 2026-06-15 Laget: 2026-06-15 Sist oppdatert: 2026-06-15bibliografisk kontrollert
Nilsson, S., Ivanoff, A., Zubairova, A., Siddanathi, L., Sepman, A., Wiinikka, H., . . . Ehn, A. (2026). Quantitative raman thermometry and N2+ detection in a non-transferred plasma torch. Optics and lasers in engineering, 200, Article ID 109583.
Åpne denne publikasjonen i ny fane eller vindu >>Quantitative raman thermometry and N2+ detection in a non-transferred plasma torch
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2026 (engelsk)Inngår i: Optics and lasers in engineering, ISSN 0143-8166, E-ISSN 1873-0302, Vol. 200, artikkel-id 109583Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Quantitative laser-based diagnostics like Raman spectroscopy are essential for studying high-temperature processes, but their application in intensely luminous and transient environments such as plasma torches is severely limited by overwhelming background emission. This study focuses on the quantitative thermometry of a 7 kW atmospheric air plasma jet, an environment where such measurements are notoriously difficult. To enable these measurements, a Polarization Lock-In Filtering (PLF) Raman technique is used to suppress the intense and fluctuating plasma background. The method successfully yields high-quality N2 ro-vibrational spectra along the jet’s central axis. Model-based fitting of these spectra produces a detailed axial temperature profile, showing a decay from over 3700 K near the nozzle. Furthermore, the high signal quality enabled the detection of singly ionized nitrogen (N2+) in the plasma core, providing direct evidence of its ionized state. These results represent the first application of PLF for thermometry in a plasma torch and provide critical experimental data for validating magnetohydrodynamic simulations. 

sted, utgiver, år, opplag, sider
Elsevier, 2026
Emneord
Thermal plasma, Plasma torch, Raman spectroscopy, Thermometry, Plasma diagnostics, Polarization lock-In filtering (PLF)
HSV kategori
Forskningsprogram
Strömningslära; Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-115897 (URN)10.1016/j.optlaseng.2025.109583 (DOI)001661218700001 ()2-s2.0-105027099558 (Scopus ID)
Forskningsfinansiär
Swedish Research Council, 2021–04506Knut and Alice Wallenberg Foundation, KAW2019.0084 COCALDSwedish Energy Agency, 49609-1, P2022-00908EU, European Research Council, 852394
Merknad

Full text license: CC BY

Tilgjengelig fra: 2026-01-08 Laget: 2026-01-08 Sist oppdatert: 2026-04-10
Siddanathi, L. S., Westerberg, L.-G., Åkerstedt, H. O., Gren, P., Wiinikka, H. & Sepman, A. (2025). Computational Analysis of Flow Separation in Non-Transferred Plasma Torch: Causes, Impacts and Control Methods. Fluids, 10(2), Article ID 47.
Åpne denne publikasjonen i ny fane eller vindu >>Computational Analysis of Flow Separation in Non-Transferred Plasma Torch: Causes, Impacts and Control Methods
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2025 (engelsk)Inngår i: Fluids, E-ISSN 2311-5521, Vol. 10, nr 2, artikkel-id 47Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

In a non-transferred plasma torch, the working gas becomes ionized and forms plasma as it interacts with the electric arc at the cathode tip. However, in certain cathode shapes, particularly flat ones, and under specific conditions, the gas flow can separate at the cathode tip, forming a vortex region. While this flow separation is influenced by geometric factors, it occurs in the critical zone where plasma is generated. Understanding the causes of this separation is essential, as it may significantly impact torch performance. If the separation proves detrimental, it is important to identify ways to mitigate it. This paper presents a computational analysis of a non-transferred plasma torch to investigate the physics behind flow separation. The results highlight the location and causes of the separation, as well as its potential advantages and disadvantages. Finally, the paper explores theoretical approaches to address flow separation in plasma torches, offering practical insights for enhancing their design and efficiency.

sted, utgiver, år, opplag, sider
MDPI, 2025
Emneord
non-transferred plasma torch, flat cathode, flow separation
HSV kategori
Forskningsprogram
Strömningslära; Experimentell mekanik; Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-111604 (URN)10.3390/fluids10020047 (DOI)001431072200001 ()2-s2.0-85218690194 (Scopus ID)
Forskningsfinansiär
Swedish Energy Agency, 49609-1
Merknad

Validerad;2025;Nivå 1;2025-02-12 (u8);

Full text license: CC BY 4.0

Tilgjengelig fra: 2025-02-12 Laget: 2025-02-12 Sist oppdatert: 2025-10-21bibliografisk kontrollert
Siddanathi, L. S., Westerberg, L.-G., Åkerstedt, H. O., Gren, P., Wiinikka, H. & Sepman, A. (2025). Computational Modeling Of Turbulent Jet Generated by Non-transferred Plasma Torch. In: SINTEF Proceedings: . Paper presented at 15th International Conference on Industrial Applications of Computational Fluid Dynamics Trondheim, Norway June 11–13, 2024 (pp. 5-12). SINTEF Academic Press
Åpne denne publikasjonen i ny fane eller vindu >>Computational Modeling Of Turbulent Jet Generated by Non-transferred Plasma Torch
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2025 (engelsk)Inngår i: SINTEF Proceedings, SINTEF Academic Press , 2025, s. 5-12Konferansepaper, Publicerat paper (Fagfellevurdert)
Abstract [en]

The plasma jet produced by a non-transferred plasma torch may initially appear steady and laminar, but it undergoes significant turbulence as it interacts with the surrounding atmosphere. Within the plasma torch, the jet begins as laminar; however, upon exiting, it transitions into a turbulent flow, extending into a long, wavy structure as it develops. This paper explores the complexities of computational modeling for non-transferred plasma torches, focusing on the challenges of simulating the multiphysics and multiphase interactions at the outlet and tracing the evolution of the plasma jet. The computational analysis uses COMSOL Multiphysics software on a 2D axisymmetric geometry, with steady-state simulations incorporating various turbulence models. A comparative assessment of the results from each turbulence model is provided, highlighting their respective strengths and limitations. Although the diffusion of the turbulent jet at the outlet is presented, the turbulence models employed in this study only offer time-averaged values, rather than a detailed breakdown of the complete jet structure. The paper concludes by validating the computationally obtained velocity magnitudes against experimental data, ensuring the accuracy and reliability of the simulation results.

sted, utgiver, år, opplag, sider
SINTEF Academic Press, 2025
HSV kategori
Forskningsprogram
Strömningslära; Experimentell mekanik; Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-111602 (URN)
Konferanse
15th International Conference on Industrial Applications of Computational Fluid Dynamics Trondheim, Norway June 11–13, 2024
Merknad

ISBN for host publication:978-82-536-1866-1

Tilgjengelig fra: 2025-02-12 Laget: 2025-02-12 Sist oppdatert: 2025-10-21bibliografisk kontrollert
Colin, S., Triana de Las Heras, F. J., Normann, F., Johansson, A., Fernberg, J., Sepman, A., . . . Wiinikka, H. (2025). Configuring hydrogen lancing to reduce carbon and nitrogen oxides emissions from coal-fired rotary kilns. International journal of hydrogen energy, 120, 323-332
Åpne denne publikasjonen i ny fane eller vindu >>Configuring hydrogen lancing to reduce carbon and nitrogen oxides emissions from coal-fired rotary kilns
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2025 (engelsk)Inngår i: International journal of hydrogen energy, ISSN 0360-3199, E-ISSN 1879-3487, Vol. 120, s. 323-332Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Coal replacement with hydrogen is a strategy for reducing carbon emissions from high-temperature industrial processes. Hydrogen lancing is a direct way for introducing hydrogen to existing coal-fired kilns. This work investigates the effects of hydrogen lancing on nitrogen oxides (NOx) emissions and ignition behaviour in a pilot-scale furnace that employs a 30 % coal replacement with hydrogen lancing. The investigation encompasses the impacts of lancing distance, angling, and velocity. Advanced measurement techniques, including spectrometry and monochromatic digital cameras, characterise the flame and assess emissions.The results indicate that the 30 % coal replacement by hydrogen lancing enhances combustion and reduces the emissions of carbon monoxides (CO). The flame characteristics vary with the location of the hydrogen injection, generally becoming more-intense than during coal combustion. NOx emissions during lancing are similar or up to double the emissions observed for pure coal combustion, depending on the lancing configuration. Increasing the distance between the hydrogen lance and coal burner increases NOx emissions.

sted, utgiver, år, opplag, sider
Elsevier, 2025
Emneord
Hydrogen, Decarbonation, Combustion, NOx, Co-firing, Rotary kiln, Integrated burner, Lancing, Solid fuel, Gaseous fuel, Spectroscopy, Photograph and video analysis
HSV kategori
Forskningsprogram
Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-112263 (URN)10.1016/j.ijhydene.2025.03.322 (DOI)001458775500001 ()2-s2.0-105001001942 (Scopus ID)
Forskningsfinansiär
Swedish Energy Agency
Merknad

Validerad;2025;Nivå 2;2025-04-08 (u4);

Funder: Luossavaara-Kiirunavaara AB (LKAB); European Union (EU) (P2022-00196);

Fulltext license: CC BY

Tilgjengelig fra: 2025-04-08 Laget: 2025-04-08 Sist oppdatert: 2025-10-21bibliografisk kontrollert
Reinsdorf, O., Vikström, T. & Wiinikka, H. (2025). Flash Calcination of Lime Mud from the Forest Industry: Influence of the Gas Atmosphere and Temperature on Calcination Behavior and Product Morphology. Industrial & Engineering Chemistry Research, 64(25), 12665-12674
Åpne denne publikasjonen i ny fane eller vindu >>Flash Calcination of Lime Mud from the Forest Industry: Influence of the Gas Atmosphere and Temperature on Calcination Behavior and Product Morphology
2025 (engelsk)Inngår i: Industrial & Engineering Chemistry Research, ISSN 0888-5885, E-ISSN 1520-5045, Vol. 64, nr 25, s. 12665-12674Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

In this article, the effects of calcination temperature and calcination atmosphere on the properties of the lime produced during flash calcination of industrial lime mud samples in a pilot-sized drop tube furnace have been studied. Flash calcination was performed at a wide range of temperatures between 800 and 1300 °C and different gas mixtures containing N2, CO2, and H2O in the calcination atmosphere. The effect of the calcination condition on the key conditions of the produced CaO, such as chemical composition, surface area, porosity, and particle morphology, has been shown. The addition of CO2 to the inert atmosphere led to slower calcination rates and a higher onset temperature for the calcination, but no changes to morphology. Furthermore, the addition of H2O to the calcination atmosphere generally led to lower calcination rates at higher temperatures and smoother particles in comparison to CO2 and N2.

sted, utgiver, år, opplag, sider
American Chemical Society (ACS), 2025
HSV kategori
Forskningsprogram
Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-113377 (URN)10.1021/acs.iecr.5c01063 (DOI)001503521300001 ()2-s2.0-105007634017 (Scopus ID)
Forskningsfinansiär
Swedish Energy Agency, 51572-1Swedish Energy Agency, P2020-00148
Merknad

Validerad;2025;Nivå 2;2025-06-30 (u2);

Full text license: CC BY

Tilgjengelig fra: 2025-06-16 Laget: 2025-06-16 Sist oppdatert: 2025-10-21bibliografisk kontrollert
Wennebro, J., Vikström, T., Reinsdorf, O. & Wiinikka, H. (2025). Influence of Feedstock Water Content on Renewable Carbon Black Production Through High-Temperature Pyrolysis of Upgraded Bio-Oils. Energy & Fuels, 39, 7805-7814
Åpne denne publikasjonen i ny fane eller vindu >>Influence of Feedstock Water Content on Renewable Carbon Black Production Through High-Temperature Pyrolysis of Upgraded Bio-Oils
2025 (engelsk)Inngår i: Energy & Fuels, ISSN 0887-0624, E-ISSN 1520-5029, Vol. 39, s. 7805-7814Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Pyrolysis oil (PO) derived from biomass has the potential to serve as a renewable feedstock for future carbon black (CB) production. However, its composition is significantly different from the fossil feedstocks currently used for CB manufacturing, as it contains higher concentrations of oxygen and water that might influence the yield and nanostructure of CB. In this article, we examine how the water content in PO affects the production of CB at high-temperature pyrolysis (1400–1600 °C) in an electrically heated entrained flow reactor. The main objective was to investigate the influence of water content on the yield and quality of the CB produced from upgraded PO with varying inherent water contents (0–20 wt %). The experiments in this work were performed with model compounds to simulate an upgraded PO. The produced CB was characterized by using several analytical techniques, including elemental composition, powder X-ray diffraction, transmission electron microscopy, and nitrogen physisorption. The results show a clear correlation between the water content in the PO feedstock and the output of CB, showing a reduced yield of CB as the water content increases. These results highlight the crucial role of feedstock composition in making PO a viable renewable feedstock for CB production.

sted, utgiver, år, opplag, sider
American Chemical Society, 2025
HSV kategori
Forskningsprogram
Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-112546 (URN)10.1021/acs.energyfuels.5c00308 (DOI)001467439700001 ()2-s2.0-105003560534 (Scopus ID)
Forskningsfinansiär
Swedish Research Council Formas, 2020-01992Bio4Energy
Merknad

Validerad;2025;Nivå 2;2025-04-29 (u5);

Full text license: CC BY 4.0;

Tilgjengelig fra: 2025-04-29 Laget: 2025-04-29 Sist oppdatert: 2026-02-12bibliografisk kontrollert
Weiland, F., Mases, M., Jacobsson, D., Wahlqvist, D., Ek, M. & Wiinikka, H. (2025). Oxidation of carbon nanomaterials using a nanoparticulate iron oxide catalyst: Direct observations in an electron microscope. Carbon, 234, Article ID 119896.
Åpne denne publikasjonen i ny fane eller vindu >>Oxidation of carbon nanomaterials using a nanoparticulate iron oxide catalyst: Direct observations in an electron microscope
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2025 (engelsk)Inngår i: Carbon, ISSN 0008-6223, E-ISSN 1873-3891, Vol. 234, artikkel-id 119896Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Understanding of carbon nanomaterials oxidation is useful in many different applications, e.g., for soot emission abatement, or in defect engineering aiming to improve material properties. In this work, the oxidative behavior of three substantially different qualities of carbon black, multiwall carbon-nanotubes, and few-layer graphene, was studied using a combination of macroscale quantification (using thermogravimetric analysis) and nanoscale imaging of their structural evolution (using environmental transmission electron microscopy, ETEM). The materials were investigated both with and without the addition of a nanoparticulate iron oxide catalyst. Catalyst addition clearly lowered the conversion temperature during oxidation. The ETEM revealed that the catalyst nanoparticles induced primary surface damages in the carbon nanostructure at relatively low temperatures. From there, oxidation could proceed more rapidly at recently exposed edge sites due to their higher propensity for oxidation. Thus, the enhanced oxidation was not solely linked to the interface between catalyst and carbon.

sted, utgiver, år, opplag, sider
Elsevier, 2025
Emneord
In situ, Electron microscope, Carbon nanomaterials, Catalytic oxidation, Iron oxide
HSV kategori
Forskningsprogram
Energiteknik
Identifikatorer
urn:nbn:se:ltu:diva-111274 (URN)10.1016/j.carbon.2024.119896 (DOI)001421292500001 ()2-s2.0-85214211083 (Scopus ID)
Forskningsfinansiär
Swedish Research Council, 2017–04902Swedish Research Council, 2020–04453
Merknad

Validerad;2025;Nivå 2;2025-01-16 (signyg);

Funder: Swedish National Infrastructure in Advanced Electron Microscopy (2021-00171, RIF21-0026);

Fulltext license: CC BY

Tilgjengelig fra: 2025-01-16 Laget: 2025-01-16 Sist oppdatert: 2025-10-21bibliografisk kontrollert
Organisasjoner
Identifikatorer
ORCID-id: ORCID iD iconorcid.org/0000-0002-9395-9928