Inert Gas Research Articles

Augmentation of hot cell facility for pyro-process of irradiated metal fuels

Hot cells with an inert atmosphere are used for handling air-sensitive, hygroscopic, and radioactive materials like mixed carbide fuels and for pyro-processing metallic fuels. Pyro-processing of spent metal fuels was based on the electrochemical recovery of actinides in high-temperature molten salts (LiCl-KCl eutectic with 58.5 mol.% LiCl). To demonstrate the remote operation feasibility of the electro-refining process of irradiated U-6 wt% Zr inside hot cells and also to study the process parameters, a pilot scale (∼100 g) pyro-process facility was set up in one of our hot cells. For this purpose, the existing hot cell facility was augmented with necessary modifications and customized to the experimental needs. This paper discusses in detail the augmentation works carried out on the existing facility to facilitate the remote operation of electro-refining of irradiated metallic fuels.

Studying the Effects of Dissolved Noble Gases and High Hydrostatic Pressure on the Spherical DOPC Bilayer Using Molecular Dynamic Simulations.

Fine-grained molecular dynamics simulations have been conducted to depict lipid objects enclosed in water and interacting with a series of noble gases dissolved in the medium. The simple point-charge (SPC) water system, featuring a boundary composed of 1,2-Dioleoyl-sn-glycero-3-phosphocholine (DOPC) molecules, maintained stability throughout the simulation under standard conditions. This allowed for the accurate modeling of the effects of hydrostatic pressure at an ambient pressure of 25 bar. The chosen pressure references the 240 m depth of seawater: the horizon frequently used by commercial divers, who comprise the primary patient population of the neurological complication of inert gas narcosis and the consequences of high-pressure neurological syndrome. To quantify and validate the neurological effects of noble gases and discriminate them from high hydrostatic pressure, we reduced the dissolved gas molar concentration to 1.5%, three times smaller than what we previously tested for the planar bilayer (3.5%). The nucleation and growth of xenon, argon and neon nanobubbles proved consistent with the data from the planar bilayer simulations. On the other hand, hyperbaric helium induces only a residual distorting effect on the liposome, with no significant condensed gas fraction observed within the hydrophobic core. The bubbles were distributed over a large volume-both in the bulk solvent and in the lipid phase-thereby causing substantial membrane distortion. This finding serves as evidence of the validity of the multisite distortion hypothesis for the neurological effect of inert gases at high pressure.

Synthesis and characterization of novel D‐mannitol based hydrogel: Swelling and adsorption behavior of heavy metal ion studies

AbstractA highly efficient hydrogel derived from D‐Mannitol xanthate has been successfully synthesized using a free‐radical solution copolymerization technique. An equimolar mixture of acrylonitrile (AN) and acrylic acid (AA) has been reacted with D‐Mannitol xanthate (DMX) under inert atmosphere. Three distinct grades of D‐Mannitol xanthate‐based hydrogels viz. DMXHGs‐1, DMXHGs‐2, and DMXHGs‐3, were prepared. Extensive analyses were conducted on the hydrogels using various methods such as UV, FT‐IR, SEM, XRD, GPC, TGA and ΔpHPZC. The maximum swelling ratio of DMXHGs‐3 was found to be 52122%, 50434% and 48576% for 24 h with water retention ratio of 80.98%, 78.64% and 79.22% for 30 h in distilled, tap and gray water respectively. These findings indicate the DMXHGs‐3 hydrogel has remarkable swelling and water retention capacity. Comprehensive investigations were carried out to evaluate the hydrogel's remarkable adsorption capacity to act as an adsorbent for effectively removing hazardous metal ions. The highest removal percentages of 95.5% and 94.4% and maximum adsorption capacities of 523.56 mg g−1 and 462.96 mg g−1 were observed with DMXHGs‐3 hydrogel for Cu2+ and Co2+ ions, respectively. Metal ion removal experiments were conducted by varying several parameters including dosage, pH, temperature, concentration, and time. The quantification of Cu2+ and Co2+ was accomplished using UV–visible spectroscopy. Present studies demonstrate the suitability of D‐mannitol xanthate‐based hydrogels for the efficient removal of toxic metal ions from wastewater.

Mathematical model for selecting the auxiliary equipment parameters of aerodynamic deorbit systems

The goal of this work is to develop a model for selecting the design parameters of auxiliary equipment for aerodynamic deorbit systems. For normal operation, an aerodynamic deorbit system, according to its class, is equipped with the following support systems: for deployment, inflation, аnd storage onboard the space object to be deorbited. The deployment system consists of two components: a mast deployment system, in which four rolled-up masts are stored and deployed, and an airfoil storage spindle, on which four quadrants of a film material are wound. Aerodynamic systems can be inflated in several ways: using a system of gas storage and supply to the shell, using the residual pressure, or using the sublimation of a powder substance. The characteristics of sublimable substances and inert gases for inflation are given. The paper presents a methodology for determining the inflating gas parameters taking into account the exposure of the aerodynamic system to space debris fragments. The following requirements are imposed on the storage system materials: resistance to space factors, resistance to dynamic loads in orbital injection, and resistance to thermal deformations. A mathematical model for selecting the auxiliary system parameters of aerodynamic deorbit systems is presented. This model includes deployment system mass estimation, relationships for determining the inflation system mass for aerodynamic systems of various configurations, wall thickness estimation for gas cylinders of different configurations, and relationships for determining the storage system mass for aerodynamic deorbit systems of different configurations.

Hierarchical porous cobalt nanoparticles encapsulated in heteroatom-doped hollow carbon as an enhancing multifunctional catalyst for hydrolysis of sodium borohydride and hydrogenation of bromate in water

Multifunctional heterogeneous catalysts have been consistently explored in recent years because of their distinctive catalytic activity in different catalysis areas at once. Here, a cobalt (Co) nanoparticles encapsulated in nitrogen-doped hollow carbon (denoted as Co@NHC) is prepared by two-step modifications of acid etching and high temperature carbonization in the inert atmosphere using a peculiar polyhedral configuration Co-ZIF as an initial template. Benefiting from an intriguing polyhedral configuration hollow structure with high specific surface area and pore volume supplying plentiful active sites, Co@NHC shows exceptional catalytic activity in catalyzing hydrolysis of NaBH4 and hydrogenation of toxic bromate in water. From experimental results, Co@NHC could efficiently enhance the generation of H2 with a H2 generation rate of 1515.4 mL min−1 gcat−1 meanwhile the activation energy (Ea) calculated from Co@NHC/NaBH4 system was only 12.6 kJ mol−1. Besides, the combination of Co@NHC and NaBH4 could further reduce toxic bromate ions into bromide via catalytic hydrogenation with a maximum bromate removal capacity of 390.6 μmol g−1. More importantly, due to its strong magnetization, Co@NHC could be simply recovered after reactions, making it well-preserve the unique structure as well as catalytic activity for multiple continuous recycles in both catalytic applications. Additionally, the plausible reaction mechanisms in catalyzing hydrolysis of NaBH4 and hydrogenation of bromate were also proposed. This work has pioneered a promising approach on preparing an engrossing magnetic heterogeneous Co-based catalyst that is practically applicable in various areas of catalysis.

Additive manufacturing inert gas flow path strategies for multi-laser powder bed fusion systems and their impact on lattice structure mechanical responses

Multi-laser Additive Manufacturing systems hold great potential to increase productivity. However, adding multiple energy sources to a powder bed fusion system requires careful selection of a laser scan and inert gas flow strategy to optimize component performance. In this work, we explore four different laser scan and argon flow strategies on the quasi-static compressive mechanical response of Body Centered Cubic lattices. Three strategies employ a swim lane method where laser pathing tends to progress parallel to argon flow. Method one only uses a single laser while method two uses four, both with the laser path working against the argon flow. The third method uses four lasers, each operating in their own lane like the second method, but the laser pathing progresses with the argon flow. The fourth method has all four lasers operating in quadrants and the laser pathing trends against the argon flow.The single-laser strategy generally had the lowest mechanical responses compared to the other three strategies. A quadrant strategy generally had the highest quasi-static mechanical responses and was at least 25% greater in stiffness, yield force, ultimate force, and energy absorption when compared to the single laser strategy. However, the four-laser swim strategy where the laser pathing tends against the argon flow was found to be statistically similar to the quadrant strategy. It is hypothesized that spatter introduced onto the powder layer from the melt pool and particle entrainment may be worse for laser pathing which trends with the argon flow direction. Additionally, the additional energy added to the build volume helps to mitigate inter-layer cool time which reduces temperature gradients. This shows that multi-laser AM systems have an impact on part performance and potentially shows lattices built with multi-laser AM systems may have certain advantages over single-laser AM systems.

Progress in Fast Modular Reactor Conceptual Design

The Fast Modular Reactor (FMR) is a 100-MW(thermal) gas-cooled fast reactor being developed by General Atomics Electromagnetic System with the goal of developing a FMR for flexible and dispatchable power to the U.S. electricity market in the mid-2030s. The conceptual design aims to develop and verify simplified design features. These include an inert helium gas coolant, pellet-loaded fuel rods, installations with air cooling as ultimate heat sink, and small and passive heat removal systems. The goal is to ensure the development of a safe, maintainable, cost-effective, and distributed nuclear energy-generating station. The baseline technologies selected to achieve this goal are a helium coolant that is an inert gas with no chemical reaction with structural components, not activated, single phase, enabling high-temperature operation and a high thermal efficiency Brayton cycle; conventional uranium dioxide (UO2) fuel, which is the most widely used and well-known fuel material, capable of high burnup (100 MWd/kg) and a long fuel life; and silicon carbide composite (SiGA®) cladding and internal structures that are chemically inert in the helium environment, exceptionally radiation tolerant, and being derisked by accident tolerant fuel technology development. The reactor was specifically designed with passive safety features, including high-temperature in-core materials and a reactor vessel cooling system consisting of cooling panels of naturally circulating water. The passive safety of the core was confirmed for the depressurized loss-of–forced cooling accident, which showed the peak cladding temperature at ~1600°C during the transient, which is below the current design limit of 1800°C. The conceptual design of the FMR has been conducted for the reactor system, vessel system, generator and turbomachine, instrumentation and control, residual heat removal system, plant service system, and containment, as well as pre-application licensing documents.

Efficient and bright broadband electroluminescence based on environment-friendly metal halide nanoclusters

Broadband electroluminescence based on environment-friendly emitters is promising for healthy lighting yet remains an unprecedented challenge to progress. The copper halide-based emitters are competitive candidates for broadband emission, but their high-performance electroluminescence shows inadequate broad emission bandwidth of less than 90 nm. Here, we demonstrate efficient ultra-broadband electroluminescence from a copper halide (CuI) nanocluster single emitter prepared by a one-step solution synthesis-deposition process, through dedicated design of ligands and subtle selection of solvents. The CuI nanocluster exhibits high rigidity in the excitation state as well as dual-emissive modes of phosphorescence and temperature-activated delayed fluorescence, enabling the uniform cluster-composed film to show excellent stability and high photoluminescent efficiency. In consequence, ultra-broadband light-emitting diodes (LEDs) present nearly identical performance in an inert or air atmosphere without encapsulation and outstanding high-temperature operation performance, reaching an emission full width at half maximum (FWHM) of ~120 nm, a peak external quantum efficiency of 13%, a record maximum luminance of ~50,000 cd m−2, and an operating half-lifetime of 137 h at 100 cd m−2. The results highlight the potential of copper halide nanoclusters for next-generation healthy lighting.

Extremely low coercivity of powder Co-rich amorphous alloy obtained by gas atomisation

A novel Co-base soft magnetic powder with ultra-low coercivity was produced by inert gas atomisation. The as-atomised powder is fully amorphous owing to its high glass forming ability and the proper selection of atomisation conditions; it exhibits a very low coercivity (0.130 Oe) mainly due to the low magnetostriction coefficient of Co-based alloys. After production, the powder was annealed at different temperatures between 300 and 600 ºC for 30 minutes. Crystallisation started at around 575 ºC, which is the temperature of the first exothermic peak detected by differential scanning calorimetry. Annealing the powder at temperatures below 550 ºC develops only structural relaxation of the amorphous structure. The smallest coercivity (0.056 Oe) was found in the sample annealed at 400 ºC. On the other hand, an increment of the coercivity of four orders of magnitude occurred after full crystallisation at 600 ºC (394.320 Oe). From the analysis of the curves of anisotropy field distribution, it can be concluded that this Co-base alloy shows lower average anisotropy field, a more gaussian shape and a wider distribution than Fe-base alloys. This is explained by a lower magnetoelastic anisotropy and a more homogeneous distribution of the magnetic anisotropy. The powder exhibits a spherical shape that makes it very suitable as ferromagnetic phase to manufacture powder cores with extremely low hysteresis loss for medium-high frequency applications.

Exploring bioenergy prospects from malt bagasse: Insights through pyrolysis with multi-component kinetic analysis and thermodynamic parameter estimation

Malt bagasse is a by-product of little commercial value in the brewing industry. Under this scenario, the current study represents the first investigation aiming to determine the kinetic triplet and thermodynamic parameters for malt bagasse pyrolysis using a multi-component kinetic approach to elucidate its bioenergy prospects. The pyrolysis progress profiles of malt bagasse were obtained through slow pyrolysis experiments on a thermogravimetric scale in an inert atmosphere, employing four distinct heating rates (10, 15, 25, and 40 °C min−1). This investigation also used the Frazer-Suzuki deconvolution function to elucidate the relative contributions of hemicellulose, cellulose, and lignin to malt bagasse pyrolysis. Activation energies for devolatilization reactions were determined by the isoconversional methods of Friedman, Flynn-Wall-Ozawa, Kissinger-Akahira-Sunose, and Starink, and revealed the lowest and highest mean values for pseudo-hemicelluloses (158.3−215.3 kJ mol−1) and pseudo-lignin (279.5−294.8 kJ mol−1), respectively. Frequency factors in malt bagasse pyrolysis ranging from 8.9 × 1016 and 2.2 × 1023 min−1 offer evidence of a simplified reaction chemistry pathway in the conversion towards bioenergy production. The integral master plot indicates the involvement of order-based and geometrical contraction-based mechanisms in malt bagasse pyrolysis. After defining multiple kinetic triplets, a differential equation encompassing contributions from all pseudo-components was formulated, and the simulated results aligned closely with experimental data, accurately describing pyrolysis progress profiles with at least 92.8% precision. The thermodynamic analysis reveals positive ΔH and ΔG values, indicating the non-spontaneous nature of malt bagasse pyrolysis. Higher disorder in the resultant products is attributed to volatile release and molecular rearrangement and is signified by positive ΔS values compared to the initial reactants. This study provided valuable insights into the valorization of malt bagasse, offering crucial information for optimizing pyrolysis reactors, scaling, and designing malt bagasse conversion into valuable biofuels, constituting an effort towards bio-circular economy principles based on the zero-waste concept.

The Influence of Various Welding Methods on the Microstructure and Mechanical Properties of 316Ti Steel.

Austenitic stainless steels are very popular due to their high strength properties, ductility, excellent corrosion resistance and work hardening. This paper presents the test results for joining AISI 316Ti austenitic steel. The technologies used for joining were the most popular welding techniques such as TIG (welding with a non-consumable electrode in the shield of inert gases), MIG (welding with a consumable electrode in the shield of inert gases) as well as high-energy EBW welding (Electron Beam Welding) and plasma PAW (plasma welding). Microstructural examinations in the face, center and root areas of the weld revealed different contents of delta ferrite with skeletal or lathy ferrite morphology. Additionally, the presence of columnar grains at the fusion line and equiaxed grains in the center of the welds was found. Microstructural, X-ray and ferroscope tests showed the presence of different delta ferrite contents depending on the technology used. The highest content of delta ferrite was found in the TIG and PAW connectors, approximately 5%, and the lowest in the EBW connector, approximately 2%. Based on the tests carried out on the mechanical properties, it was found that the highest properties were achieved by the MIG joint (Rm, 616, Rp0.2 = 335 MPa), while the lowest were achieved by the PAW joint (Rm = 576, Rp0.2 = 315 MPa).

Origin of extended visible light absorption in nitrogen-doped CuTa2O6 perovskites: the role of copper defects

Abstract The optical band gap of the semiconductor CuTa2O6, synthesised via solid-state reaction, can be greatly reduced by annealing in ammonia, which leads to a significant red-shift of the visible light absorption. Using X-ray photoelectron spectroscopy (XPS), we have shown that this absorption extension does not result from the incorporation of nitrogen, but can be attributed to copper defects formed under the reducing conditions of ammonia treatment. Photocatalytic hydrogen evolution experiments were used to investigate the influence of these defects on the photocatalytic performance. We have further shown that CuTa2O6 with similar increased visible light absorption can be prepared by annealing with an organic reducing agent – sodium citrate – in inert gas atmosphere.

Penetration identification of magnetic controlled Keyhole Tungsten inert gas horizontal welding based on OCR-SVM

Penetration identification of magnetic controlled Keyhole Tungsten inert gas horizontal welding based on OCR-SVM

Recycle process and industrial use of pyrolytic oil from waste tire pyrolysis

ABSTRACT With the developments in the automotive sector and the increase in the number of automobiles, the need to dispose of expired tires has also increased. Operations such as the storage and transportation of waste tires without harming the environment cause great costs. The present study investigated the availability of products that can be obtained through thermochemical processes from waste tires that have reached the end of their lifespan. The tires were pyrolyzed in an inert gas environment at high temperatures to obtain pyrolytic oil, carbon black, and gas. It was aimed at increasing the product quality by adding different brands of sediment crushers and 2-ethyl-hexyl-nitrate from different countries at various ratios to the pyrolytic oil obtained. The RON and MON values of the product were 92.8 and 78.9, respectively. These results show that it is possible to improve the light product fraction to be close to gasoline specifications by blending with conventional gasoline fuel. Moreover, the product has a density of 989.9 kg/m3 and can be blended with marine fuels by the relevant standards with 4.68% carbon residue values, so that pyrolysis fuel can also find use in the shipping industry. Waste gas, one of the outputs of the pyrolysis process, was also evaluated within the scope of this study. It was mixed with pyrolysis fuel and used for fuel enrichment (80% pyrolytic oil + 20% pyrolytic gas). Although it produces less torque and power than conventional diesel fuel, it is concluded that the combustion characteristics of the engine can be improved compared to the use of pyrolytic oil alone as fuel. Because of the study, an alternative fuel was obtained by evaluating both the disposal of waste tires and the liquid and gaseous components released as a result of disposal.

Wear Behavior Assessment of New Wire-Arc Additively Manufactured Surfaces on AA6061 and AA5086 Alloys through Multi-Walled Carbon Nanotubes and Ni Particles Inducement

This study investigates the new surface development on AA6061 and AA5086 alloys considering the wire-arc additive manufacturing technique as a direct energy deposition (DED) process of wire. Two different quantities of MWCNTs, i.e., 0.01 (low) and 0.02 (high) g, with a constant nickel (Ni) weight (0.2 g) were pre-placed in the created square patterns. ER4043 filler was used as a wire for additive deposition, and an arc was generated through a tungsten inert gas (TIG) welding source. Furthermore, hardness and pin-on-disk wear-testing methods were employed to measure the changes at the surfaces with the abovementioned inducements. This work was designed to illustrate the hardness and the offered wear resistance in terms of mass loss of the AA6061 and AA5086 aluminum alloys with the function of nano-inducements. Two sliding distance values of 500 m and 600 m were selected for the wear analysis of mass loss from tracks. A maximum increase in hardness for AA6061 and AA5086 alloys was observed in the experiments, with average values of 70.76 HRB and 74.86 HRB, respectively, at a high mass content of MWCNTs. Moreover, the tribological performance of the modified surfaces improved with the addition of MWCNTs with Ni particles in a broader sense; the modified surfaces performed exceptionally well for AA5086 compared to AA6061 with 0.02 and 0.01 g additions, respectively. The system reported a maximum of 38.46% improvement in mass loss for the AA5086 alloy with 0.02 g of MWCNTs. Moreover, the morphological analysis of the developed wear tracks and the mechanism involved was carried out using scanning electron microscope (SEM) images.

Trialkoxysilane-Induced Iridium-Catalyzed para-Selective C–H Bond Borylation of Arenes

An ideal approach for the construction of aryl boron compounds is to selectively replace a C–H bond in arenes with a C–B bond, and controlling regioselectivity is one of the most challenging aspects of these transformations. Herein, we report an iridium-catalyzed trialkoxysilane protecting group-assisted regioselective C–H borylation of arenes, including derivatives of benzaldehydes, acetophenones, benzoic acids, benzyl alcohols, phenols, aryl silanes, benzyl silanes, and multi-functionalized aromatic rings are all well tolerated and gave the para -selective C–H borylation products in a short time without the requirement of inert gases atmosphere. The site-selective C–H borylation can be adjustable by installing the developed trialkoxysilane protecting group on different functional groups on one aromatic ring. Importantly, the preparation process of the trialkoxychlorosilane is efficient and scalable. Mechanistic and computational studies reveal that the steric hindrance of the trialkoxysilane protecting group plays a key role in dictating the para-selectivity.

Mine Fires, Experiences in Extinguishing Large Underground Mine Fires

Mine fires are common the underground exploitation of mineral raw materials. With the development of mining science and practice, the methods of extinguishing mine fires using new methods and materials were also developed. Today, in mining practice, direct fire extinguishing with water or fire extinguishers, isolation of oxidation zones with insulating walls, installation of torket concrete on the walls of the pit room or use of special foams are most often used. Methods based on ventilation methods or the use of inert gases can also be encountered. All these methods are used to extinguish local oxidation processes, fires are localized in a part of the pit, ventilation department or goafs. This paper presents methods of extinguishing a mine fire where the fire zone covered a larger area and it was not possible to localize it in one part of the underground mine, the pit is completely closed and isolated until the oxidation process subsides due to lack of oxygen. At the time of the complete closure and isolation of the pit, several gas detectors remained in operation in the pit, through which the change in the composition of the pit air could be monitored during the still active pit fire. At the same time, samples of the pit atmosphere behind the isolation walls were regularly taken, their analysis was performed and they were compared with the data obtained using active gas detectors. The key question was when to reopen the pit, conduct an inspection and try to reactivate the pit operations. Although it is an underground brown coal mine, some experiences and knowledge can be applied and used in underground mines of other mineral resources threatened by pit fires. Experiences can also be applied in case of fire, where it is possible to control the fire zone only through insulating walls. It was established that changes in the activity of the pit fire were manifested both on the insulation walls and on the active gas detectors.

Enhanced electrical performance of LiMnPO4 by carbon coating for solid-state battery applications

High-energy ball milling was employed to fabricate LiMnPO4 coated with varying carbon ratios (3%wt, 7%wt, and 10%wt), using glucose as a carbon source. The process involved pre-milling of LiMnPO4 precursors, followed by granulation through high-energy ball milling at 270 rpm for 2 h, and subsequent calcination at 700 °C without an inert gas flow. XRD analysis discerned the phases and structure of LiMnPO4, confirming the successful attainment of a single-phase LiMnPO4 without impurities. Rietveld refinement of the XRD data elucidated the crystallographic details, affirming the material's orthorhombic olivine structure with precise lattice parameters, thereby underpinning the structural integrity essential for electrochemical applications. FE-SEM analysis revealed uniformly distributed semi-sphere particles, with sizes ranging from 130 nm for LM to 183 nm for LM-10%C. FTIR analysis delineated the internal modes of vibration in the olivine structure and verified the presence of carbon on the powder surface. Electrical measurements conducted within the frequency range of 20 Hz–100 kHz demonstrated an increase in electrical conductivity with an escalation in carbon concentration, ranging from 31 μΩ−1m−1 to 75 μΩ−1m−1 for 0%C and 10%C, respectively. A temperature-dependent study spanning 30–160 °C revealed stable electrical conductivity behavior for the samples, with a marginal increase observed at elevated temperatures.

Solar Energy Driven Chemical Looping Air Separation

Chemical looping is emerging as a feasible alternative to carry out reduction and oxidation processes under different process conditions. This technology proves especially useful when reduction and oxidation processes proceed with different time constants. With the possibility of incorporation of solar energy to the endothermic end of the process, chemical looping technology has recently become more popular. Chemical looping air separation (CLAS) is an alternative to cryogenic separation, by utilizing solar thermal energy. In this process a reducible metal oxide is heated to a temperature such that the metal releases its lattice oxygen. In the second step, the metal oxide is exposed to air and oxygen is captured by the oxide while pure nitrogen is released at the outlet and the loop is closed. Mn2O3 is selected as the oxygen carrier to perform chemical looping cycles. Oxygen mobility of the metal oxide and reversibility through redox cycles are tested with thermogravimetric analysis (TGA). The redox cycles are designed such that the air oxidizes, and the steam reduces the material. The reduction behavior of manganese (III) oxide under inert atmosphere is tested in TGA. It is proved that steam acts as an inert gas under the reaction conditions. The use of steam at the reduction stage results in a more convenient separation of the sweep gas (steam) from the oxygen released from the oxide. It is demonstrated that a redox cycle between Mn2O3 and Mn3O4 can be performed isothermally. The capability of the system to be coupled with solar energy makes it more alluring for environmentally friendly option seekers. The use of solar irradiation is tested with parabolic mirrors to observe the power output. Overall, CLAS process works on milder conditions which is crucial in reducing the energy and equipment costs, and its advantages regarding energy efficiency increase even more when solar energy is incorporated into the system.

Inertization parameters for alcohols and ketones with nitrogen and carbon dioxide

A flammable fuel/air mixture can be successfully prevented from entering the explosion range of concentration by the addition of an inert gas. This method of inertization is commonly used in industrial plants to keep processes safe. For this purpose, the oxygen concentration in the over-all mixture is often monitored, taking an appropriate safety margin into account. The mixture would not become flammable, independent of the amount of fuel added, while the oxygen content is below the so-called limiting oxygen concentration (LOC). The aim of this paper is to investigate the inertization-related characteristics of the two different inert gases nitrogen (N2) and carbon dioxide (CO2). The LOC of a series of alcohols and ketones was therefore measured. The experimental determination of the LOCs was carried out according to EN 1839 (2017) using the tube method at ambient initial pressure and suitable initial temperature to evaporate the liquid sample. Triangular diagrams, which represent the explosion ranges, were constructed from the results and additional inertization-related parameters derived: the minimum inert gas/air ratio (IAR) and the minimum inert gas/combustible gas ratio (ICR). It is well-known that carbon dioxide exhibits a stronger inerting effect than nitrogen. In agreement, the ratio LOC(CO2)/LOC(N2) was now determined to be a constant value of 1.33 ± 0.04 in the applied temperature range at ambient pressure. In inertization applications, this ratio in future helps to calculate LOC(CO2) from the much more often known LOC(N2).