Abstract:The development of an efficient process to simultaneously extract oxygen and metals from lunar regolith by way of in-situ resource utilisation (ISRU) has the potential to enable sustainable activities beyond Earth. The Metalysis-FFC (Fray, Farthing, Chen) process has recently been proven for the industrial-scale production of metals and alloys, leading to the present investigation into the potential application of this process to regolith-like 2 materials. This paper provides a proof-of-concept for the electro… Show more
“…This condition is in contrast to that of the electro-reduction of TiO 2 , whose perovskitization results in the increased volume of the solid phase and hence blockage of the pores in the oxide cathode, impeding the removal of O 2− and the whole electrolysis. Continuous CaTiO 3 electrolysis via Reaction (16) will lead to the accumulation of CaO in the molten salt. However, one can in principle combine Reactions ( 16) and ( 13) to form a closed loop in which CaO is cycled and functions like a "phase change catalyst" to accelerate the electrolysis of TiO 2 .…”
Section: Perovskitization Of Metal Oxides On Cathodementioning
confidence: 99%
“…In the past two decades, world-wide research and development have confirmed the scientific principle and technical feasibility and flexibility of the process for the extraction of almost all metals listed in the periodic table and their alloys from their respective oxide or sulfide precursors [6][7][8][9][10][11][12][13][14]. In addition, the FFC Cambridge Process has versatile applications in other fundamental and industrial areas, such as near-net shape manufacturing of metallic artifacts of complex structures, medical implants, oxygen generation on the moon, capture and electrolytic conversion of carbon dioxide (CO 2 ) to various forms of carbon, e.g., carbon nanotubes, carbon monoxide (CO), and hydrocarbon fuels (C n H 2n+2 , n < 10), and rechargeable molten salt metal-air batteries [15][16][17][18][19][20][21][22].…”
Molten salts play multiple important roles in the electrolysis of solid metal compounds, particularly oxides and sulfides, for the extraction of metals or alloys. Some of these roles are positive in assisting the extraction of metals, such as dissolving the oxide or sulfide anions, and transporting them to the anode for discharging, and offering the high temperature to lower the kinetic barrier to break the metal-oxygen or metal-sulfur bond. However, molten salts also have unfavorable effects, including electronic conductivity and significant capability of dissolving oxygen and carbon dioxide gases. In addition, although molten salts are relatively simple in terms of composition, physical properties, and decomposition reactions at inert electrodes, in comparison with aqueous electrolytes, the high temperatures of molten salts may promote unwanted electrode-electrolyte interactions. This article reviews briefly and selectively the research and development of the Fray-Farthing-Chen (FFC) Cambridge Process in the past two decades, focusing on observations, understanding, and solutions of various interactions between molten salts and cathodes at different reduction states, including perovskitization, non-wetting of molten salts on pure metals, carbon contamination of products, formation of oxychlorides and calcium intermetallic compounds, and oxygen transfer from the air to the cathode product mediated by oxide anions in the molten salt.
“…This condition is in contrast to that of the electro-reduction of TiO 2 , whose perovskitization results in the increased volume of the solid phase and hence blockage of the pores in the oxide cathode, impeding the removal of O 2− and the whole electrolysis. Continuous CaTiO 3 electrolysis via Reaction (16) will lead to the accumulation of CaO in the molten salt. However, one can in principle combine Reactions ( 16) and ( 13) to form a closed loop in which CaO is cycled and functions like a "phase change catalyst" to accelerate the electrolysis of TiO 2 .…”
Section: Perovskitization Of Metal Oxides On Cathodementioning
confidence: 99%
“…In the past two decades, world-wide research and development have confirmed the scientific principle and technical feasibility and flexibility of the process for the extraction of almost all metals listed in the periodic table and their alloys from their respective oxide or sulfide precursors [6][7][8][9][10][11][12][13][14]. In addition, the FFC Cambridge Process has versatile applications in other fundamental and industrial areas, such as near-net shape manufacturing of metallic artifacts of complex structures, medical implants, oxygen generation on the moon, capture and electrolytic conversion of carbon dioxide (CO 2 ) to various forms of carbon, e.g., carbon nanotubes, carbon monoxide (CO), and hydrocarbon fuels (C n H 2n+2 , n < 10), and rechargeable molten salt metal-air batteries [15][16][17][18][19][20][21][22].…”
Molten salts play multiple important roles in the electrolysis of solid metal compounds, particularly oxides and sulfides, for the extraction of metals or alloys. Some of these roles are positive in assisting the extraction of metals, such as dissolving the oxide or sulfide anions, and transporting them to the anode for discharging, and offering the high temperature to lower the kinetic barrier to break the metal-oxygen or metal-sulfur bond. However, molten salts also have unfavorable effects, including electronic conductivity and significant capability of dissolving oxygen and carbon dioxide gases. In addition, although molten salts are relatively simple in terms of composition, physical properties, and decomposition reactions at inert electrodes, in comparison with aqueous electrolytes, the high temperatures of molten salts may promote unwanted electrode-electrolyte interactions. This article reviews briefly and selectively the research and development of the Fray-Farthing-Chen (FFC) Cambridge Process in the past two decades, focusing on observations, understanding, and solutions of various interactions between molten salts and cathodes at different reduction states, including perovskitization, non-wetting of molten salts on pure metals, carbon contamination of products, formation of oxychlorides and calcium intermetallic compounds, and oxygen transfer from the air to the cathode product mediated by oxide anions in the molten salt.
“…The process has since been shown to be capable of reducing many different metal oxides, including those of tantalum, chromium and cerium [2][3][4]. Mixed-metal oxides can also be reduced simultaneously, allowing for the direct production of alloys, as well as more novel materials like high-entropy alloys and those derived from lunar regolith simulant material [5][6][7][8][9].…”
Section: Ti Extraction Via the Ffc-cambridge Processmentioning
Combining the FFC-Cambridge process with field-assisted sintering technology (FAST) allows for the realisation of an alternative, entirely solid-state, production route for a wide range of metals and alloys. For titanium, this could provide a route to produce alloys at a lower cost compared to the conventional Kroll-based route. Use of synthetic rutile instead of high purity TiO2 offers further potential cost savings, with previous studies reporting on the reduction of this feedstock via the FFC-Cambridge process. In this study, mixtures of synthetic rutile and iron oxide (Fe2O3) powders were co-reduced using the FFC-Cambridge process, directly producing titanium alloy powders. The powders were subsequently consolidated using FAST to generate homogeneous, pseudo-binary Ti–Fe alloys containing up to 9 wt.% Fe. The oxide mixture, reduced powders and bulk alloys were fully characterised to determine the microstructure and chemistry evolution during processing. Increasing Fe content led to greater β phase stabilisation but no TiFe intermetallic phase was observed in any of the consolidated alloys. Microhardness testing was performed for preliminary assessment of mechanical properties, with values between 330–400 Hv. Maximum hardness was measured in the alloy containing 5.15 wt.% Fe, thought due to the strengthening effect of fine α phase precipitation within the β grains. At higher Fe contents, there was sufficient β stabilisation to prevent α phase transformation on cooling, leading to a reduction in hardness despite a general increase from solid solution strengthening.
“…As shown recently [15], the so-called FFC Cambridge electrolytic process can be used to separate earthly, lunar or asteroid rock into oxygen gas and a solid residue comprising metals and silicon. The oxygen can be used as Electric Propulsion propellant [16].…”
Section: Asteroid Materials Transferred By O 2 Electric Propulsionmentioning
We present a two-sphere dumbbell configuration of a rotating settlement at Earth-Moon L5. The two-sphere configuration is chosen to minimize the radiation shielding mass which dominates the mass budget. The settlement has max 20 mSv/year radiation conditions and 1 g artificial gravity. If made for 200 people, it weighs 89000 tonnes and provides 60 m 2 of floorspace per person. The radiation shield is made of asteroid rock, augmented by a water layer with 2 % of the mass for neutron moderation, and a thin boron-10 layer for capturing the thermalized neutrons. We analyze the propulsion options for moving the material from asteroids to L5. The FFC Cambridge process can be used to extract oxygen from asteroid regolith. The oxygen is then used as Electric Propulsion propellant. One can also find a water-bearing asteroid and use water for the same purpose. If one wants to avoid propellant extraction, one can use a fleet of electric sails. The settlers fund their project by producing and selling new settlements by zero-delay teleoperation in the nearby robotic factory which they own. The economic case looks promising if LEO launch costs drop below ∼ $300/kg.
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