Reaction Of CO Research Articles

Theoretical study of temperature and pressure-dependent rate constants for 8 reactions involving CO and CO2 with C+, C2O2+, CnO3, CnO3+ (n = 1, 2) in carbon dioxide radiolysis

CO2-related reactions and their species play an important role in atmospheric and radiolysis chemistry. However, there remains a lack of temperature and pressure dependent reaction rates for many chemical reactions that are necessary for constructing relevant reaction mechanisms. 8 important atmospheric and radiolysis chemical reactions are investigated theoretically at the rev-DSD/j3z, CCSD/ACCD and CCSD(T)/CBS levels. The temperature, pressure-dependent rate constants are obtained by the RRKM/ME method, which show a reasonable agreement with the reported values. Based on our results, the mechanisms of correlation reaction of CO2 reaction network are refined and provide guidance for studying the directed conversion of CO2.

Nanoporous Copper for the Electrosynthesis of Cyclic Carbonates from CO2 and Epoxides

AbstractCyclic carbonates are often produced through catalytic coupling reactions of CO2 with epoxides under harsh conditions. Here, we present a highly active nanoporous copper (np‐Cu) cathode material for the electrosynthesis of cyclic carbonates in mild environments. Np−Cu material was drop casted on glassy carbon (np‐Cu/GC) as cathode electrode to perform galvanostatic electrosynthesis using a magnesium anode in CO2‐saturated acetonitrile with 0.1 M tetraethylammonium iodide. Very good yields have been obtained for 1,2‐butylene carbonate (BC, 74 ± 4 %) and propylene carbonate (PC, 62 ± 6 %). By varying the cathode electrode materials, low yields (≤ 20 %) on bare GC, but similar yields (76 ± 4 % BC and 63 ± 5 % PC) on polycrystalline Cu were achieved. Although the pore‐ligament structure is beneficial to enhance the CO2RR performance, its impact on the yield of cyclic carbonate is minimal. This implies that the activation of CO2 to the CO2⋅− radical anion is not the rate‐limiting step, but rather the ring closure of the final intermediate to form cyclic carbonates. Moreover, the np‐Cu/GC shows very good stability and reusability for the electrochemical‐organic test reaction. This study provides deeper insights into the reaction mechanism of cyclic carbonates formation on Cu‐based electrodes.

Upcycling Waste Biomass–Production of Porous Carbonaceous Supports from Paper Mill Sludge and Application to CO2 Conversion

AbstractThe urgent need for sustainable waste management strategies has led to the exploration of innovative approaches for the valorization of waste. In this study, a method is proposed for carbonizing waste biomass materials, particularly paper mill waste sludges (primary and biological) and knots, to produce porous carbonaceous supports. Through an initial hydrothermal carbonization followed by carbonization with nitrogen flow, porous carbon materials are successfully generated. The findings of this investigation validate the successful generation of effective carbonaceous supports utilizing waste biomass materials. These materials are then evaluated for their effectiveness as porous supports in the ionic liquid‐catalyzed cycloaddition reaction of CO2 to styrene oxide, achieving a remarkable conversion rate of up to 98% and an impressive selectivity exceeding 99%. Additionally, the results underscore the significant impact of the selected IL on the overall conversion process. Overall, this study presents a promising pathway for the valorization of paper mill waste sludge through the production of porous carbon materials with potential applications in catalysis and beyond.

Mesoporous TS-1 zeolite-confined metal oxides photocathode for efficient reduction of carbon dioxide to methanol

Excessive CO2 emission has caused serious environmental problems, and converting CO2 to high value-added fuels is attractive for solving energy and environmental crisis. Herein, a novel mesoporous TS-1(mTS-1) zeolite-confined metal oxides nanoclusters Cu-Bi@mTS-1 was developed for efficient photoelectrochemical reduction reaction of CO2 (PEC CO2RR). The catalyst Cu-Bi@mTS-1 as a photocathode showed high activity, achieving a maximum methanol Faraday efficiency (FECH3OH) of 93.4 % at −0.7 V vs. RHE. The C2 product ethanol could be also detected at higher potentials during PEC CO2RR. In-situ FTIR results indicate the occurrence of key reaction intermediates *CO, *CHO, *OCCO and *COCHO during the conversion of CO2 to CH3OH and CH3CH2OH. It is believed that the hierarchically porous structure of mTS-1 is conducive to the enrichment of CO2 molecules to increase the reactant concentration, also can promote C-C coupling through photoelectric synergism. This work provides a favorable reference for the rational design of photocathodes by confinement effect of porous structure.

Synthesis and characterization of catalytic active oxazolidine/Schiff complexes using 2-quinoline formaldehyde and tris-base for carbon dioxide chemical fixation

Catalytic chemical fixation of carbon dioxide to high value-added chemicals has attracted extensive attention and the discovery of new catalytic system has always been a research hotspot in carbon dioxide chemistry. Three complexes were synthesized by using 2-quinoline formaldehyde and tris-base precursor through Schiff base reaction and characterized. Compound Co[L1]2Cl2·2H2O (1) and compound Ni[L1]2Cl2·2H2O (2) are two mononuclear complex with derived schiff base ligand (L1 = 2-(hydroxymethyl)-2-((quinolin-2-ylmethylene)amino)propane-1,3-diol), while compound Cu2[L2]2Cl2∙2CH3OH (3) is a dinuclear complex containing derived deprontonated ligand (L2 = (2-(quinolin-2-yl)oxazolidine-4,4-diyl)dimethanol) The self-assembly process of these complexes were monitored by ESI-MS. The catalytic explore for the cycloaddition of CO2 and different reaction substrates and preliminary kinetic studies shows that all complexes are active and the reaction is an intramolecular Lewis acid-base catalytic mechanism. This is the first report of oxazolidine complex/ tetrabutylammonium halide catalyst in for cycloaddition of epoxides and CO2 reaction and the complex 3 is more active than the other two complexes, which provides new notions for the design and solicitation of Schiff base/oxazolidine catalysts.

Synthesis, crystal structure and thermal properties of the dinuclear complex bis-(μ-4-methylpyridine N-oxide-κ2O:O)bis-[(methanol-κO)(4-methylpyridine N-oxide-κO)bis-(thio-cyanato-κN)cobalt(II)

Reaction of Co(NCS)2 with 4-methyl-pyridine N-oxide in methanol leads to the formation of crystals of the title compound, [Co2(NCS)4(C6H7NO)4(CH4O)2] or Co2(NCS)4(4-methyl-pyridine N-oxide)4(methanol)2. The asymmetric unit consist of one CoII cation, two thio-cyanate anions, two 4-methyl-pyridine N-oxide coligands and one methanol mol-ecule in general positions. The H atoms of one of the methyl groups are disordered and were refined using a split model. The CoII cations octa-hedrally coordinate two terminal N-bonded thio-cyanate anions, three 4-methyl-pyridine N-oxide coligands and one methanol mol-ecule. Each two CoII cations are linked by pairs of μ-1,1(O,O)-bridging 4-methyl-pyridine N-oxide coligands into dinuclear units that are located on centers of inversion. Powder X-ray diffraction (PXRD) investigations prove that the title compound is contaminated with a small amount of Co(NCS)2(4-meth-yl-pyridine N-oxide)3. Thermogravimetric investigations reveal that the methanol mol-ecules are removed in the beginning, leading to a compound with the composition Co(NCS)2(4-methyl-pyridine N-oxide), which has been reported in the literature and which is of poor crystallinity.

Facet and dual vacancy engineering-boosting BiOBr for enhanced CO2 and epoxide cycloaddition reaction under mild and cocatalyst-free conditions: Double substrate active sites and activated surface bromine ions synergy

Among the many strategies for CO2 resource utilization, the synthetic technology of cyclic carbonates with 100 % atom economy through CO2and epoxide is one of the most industrially viable routes, but its efficiency has been severely hampered by the lack of highly active catalytic sites. Moreover, due to the intrinsic thermodynamic stability and kinetic inertia of CO2 and the higher energy barrier of the ring-opening reaction of epoxides, the heterogeneous catalytic conversion of CO2 highly depends on harsh operating conditions, high temperatures and pressures, and the incorporation of cocatalysts. The development of efficient heterogeneous catalysts for CO2 conversion under cocatalyst-free and mild conditions has always been a challenge. Herein, we have proposed a synergetic strategy of facet and vacancy engineering for the construction of highly efficient heterogeneous catalyst BiO1-xBr1-y-(010) for CO2 cycloaddition, where introducing the OVs-BrVs pairs into typical (010) facets BiOBr with simultaneous surface Lewis acid sites Bi3+ and nucleophilic sites Br−. By combining theoretical calculations and a series of systematic experiments, such as CO2 temperature-programmed desorption, electron paramagnetic resonance and fluorescence probe analysis experiments, the introduced OVs-BrVs pair can not only form Bi3+-Bi(3-x)+ dual active sites on the surface, which activate PO and CO2 respectively to reduce the energy barrier of CO2 insertion, but also activate Br− near BrVs to enhance their nucleophilic attacking ability and reduce the energy barrier of epoxides ring-opening. As a result, the BiO1-xBr1-y-(010) with abundant surface OVs-BrVs pairs showed a high cyclic carbonates conversion of 99 % with 100 % selectivity under cocatalyst-free and mild conditions, far surpassing most heterogeneous catalytic systems. This work provides a completely new strategy to construct high-performance heterogeneous CO2 cycloaddition catalysts through a simple facet and vacancy engineering strategy to overcome the harsh operating conditions limitation and the use of cocatalysts.

In-situ precipitation zero-valent Co on Co2VO4 to activate oxygen vacancies and enhance bimetallic ions redox for efficient detection toward Hg(II)

Despite the widespread utilization of variable valence metals in electrochemistry, it is still a formidable challenge to enhance the valence conversion efficiency to achieve excellent catalytic activity without introducing heterophase elements. Herein, the in-situ precipitation of Co particles on Co2VO4 not only enhanced the concentration of oxygen vacancies (Ov) but also generated a greater number of low-valence metals, thereby enabling efficient reduction towards Hg(II). The electroanalysis results demonstrate that the sensitivity of Co/Co2VO4 towards Hg(II) was measured at an impressive value of 1987.74 μA μM−1 cm−2, significantly surpassing previously reported results. Further research reveals that Ov acted as the main adsorption site to capture Hg(II). The redox reactions of Co2+/Co3+ and V3+/V4+ played a synergistic role in the reduction of Hg(II), accompanied by the continuous supply of electrons from zero-valent Co to expedite the valence cycle. The Co/Co2VO4/GCE presented remarkable selectivity towards Hg(II), with excellent stability, reproducibility, and anti-interference capability. The electrode also exhibited minimal sensitivity fluctuations towards Hg(II) in real water samples, underscoring its practicality for environmental applications. This study elucidates the mechanism underlying the surface redox reaction of metal oxides facilitated by zero-valent metals, providing us with new strategies for further design of efficient and practical sensors.

Synthesis of PEI Grafted Poly (Ionic Liquid)s: Optimization and Kinetics Modeling of Effective CO2 Fixation Reactions

AbstractFixing the greenhouse gas CO2 through epoxide helps to mitigate worldwide ecological troubles. The applications of metal‐free and solvent‐free catalysts remain a challenge for CO2 catalytic conversion. In this work, an array of quaternary ammonium salts derived from polyethyleneimine with hydroxyl groups ([PEI‐GDMAB‐Cn]Br) were constructed by the reaction of branched PEI with a molecular weight of 10000 and glycidyl alkyl dimethylammonium bromide. A range of experiments were designed to demonstrate that [PEI‐GDMAB‐Cn]Br can be considered as a valid metal‐free and solvent‐free homogeneous catalyst for the CO2‐epoxide cycloaddition reaction. Among of [PEI‐GDMAB‐Cn]Br, [PEI‐GDMAB‐C18]Br catalyzed the model reaction of CO2 and epichlorohydrin under optimized reaction conditions (T=80 °C, 1.0 atm CO2, catalyst 1 mol%, ECH 15 mmol, 16 h) and the conversion achieved at 97.5 %. Moreover, the catalyst exhibited stable reusability and broad substrate applicability, which was used in the following cycle succinctly, because of self‐separated properties by temperature control. The [PEI‐GDMAB‐C18]Br catalyzed reaction process was detected as a pseudo‐first‐order reaction after kinetic studies and an Ea was calculated to be 50.65 kJ/mol. A combinatorial catalytic mechanism of hydrogen bonding and bromide ions is suggested to explain the remarkable catalytic performance of this bifunctional catalyst.

A novel PVI-PVA/PS composite membrane modified by metal ions for CO2 separation: Effect and mechanism

The membrane process is potentially more energy-efficient than conventional separation technologies in the separation of carbon dioxide (CO2) /nitrogen (N2) from flue gas. In this work, a series of PVI (Polyvinylimidazole)-PVA (Polyvinyl alcohol) /PS (Polysulfone) membranes were prepared by co-blending two polymers, PVI and PVA, as the separation layer of the fixed carrier composite membrane. The separation performance increased by the dual action of PVA and the imidazole group in the PVI. Furthermore, Mg2+-PVI-PVA/PS and Cu2+-PVI-PVA/PS composite membranes were developed by adding Mg2+ and Cu2+, and the separation performance was considerably improved by complexing metal ions with PVA and PVI. Especially, Mg2+-PVI-PVA/PS demonstrated superior separation performance, with a CO2 permeation rate of 12 GPU and a CO2/N2 separation factor of 183 at a pressure of 1 bar. What’s more, the mechanism study clarified that the prepared composite membrane mainly relies on the facilitated transfer mechanism to achieve the selective separation of CO2. The presence of water molecules significantly improved the CO2 permeability and separation selectivity, indicating that PVI-PVA and Mg2+ could promote the hydration reaction of CO2 and H2O, forming easily mobile HCO3- carriers.

Synthesis, crystal structure and properties of the trigonal-bipyramidal complex tris-(2-methyl-pyridine N-oxide-κO)bis-(thio-cyanato-κN)cobalt(II).

Reaction of Co(NCS)2 with 2-methyl-pyridine N-oxide in a 1:3 ratio in n-butanol leads to the formation of crystals of tris-(2-methyl-pyridine N-oxide-κO)bis-(thio-cyanato-κN)cobalt(II), [Co(NCS)2(C6H7NO)3]. The asymmetric unit of the title compound consists of one CoII cation two thio-cyanate anions and three crystallographically independent 2-methyl-pyridine N-oxide coligands in general positions. The CoII cations are trigonal-bipyramidally coordinated by two terminal N-bonding thio-cyanate anions in the trans-positions and three 2-methyl-pyridine N-oxide coligands into discrete complexes. These complexes are linked by inter-molecular C-H⋯S inter-actions into double chains that elongate in the c-axis direction. Powder X-ray diffraction (PXRD) measurements prove that all batches are always contaminated with an additional and unknown crystalline phase. Thermogravimetry and differential analysis of crystals selected by hand reveal that the title compound decomposes at about 229°C in an exothermic reaction. At about 113°C a small endothermic signal is observed that, according to differential scanning calorimetry (DSC) measurements, is irreversible. PXRD measurements of the residue prove that a poorly crystalline and unknown phase has formed and thermomicroscopy indicates that some phase transition occurs that is accompanied with a color change of the title compound.

Synergistic Effect of CO2 in Accelerating the Galvanic Corrosion of Lithium/Sodium Anodes in Alkali Metal-Carbon Dioxide Batteries.

Rechargeable alkali metal-CO2 batteries, which combine high theoretical energy density and environmentally friendly CO2 fixation ability, have attracted worldwide attention. Unfortunately, their electrochemical performances are usually inferior for practical applications. Aiming to reveal the underlying causes, a combinatorial usage of advanced nondestructive and postmortem characterization tools is used to intensively study the failure mechanisms of Li/Na-CO2 batteries. It is found that a porous interphase layer is formed between the separator and the Li/Na anode during the overvoltage rising and battery performance decaying process. A series of control experiments are designed to identify the underlying mechanisms dictating the observed morphological evolution of Li/Na anodes, and it is found that the CO2 synergist facilitates Li/Na chemical corrosion, the process of which is further promoted by the unwanted galvanic corrosion and the electrochemical cycling conditions. A detailed compositional analysis reveals that the as-formed interphase layers under different conditions are similar in species, with the main differences being their inconsistent quantity. Theoretical calculation results not only suggest an inherent intermolecular affinity between the CO2 and the electrolyte solvent but also provide the most thermodynamically favored CO2 reaction pathways. Based on these results, important implications for the further development of rechargeable alkali metal-CO2 batteries are discussed. The current discoveries not only fundamentally enrich our knowledge of the failure mechanisms of rechargeable alkali metal-CO2 batteries but also provide mechanistic directions for protecting metal anodes to build high-reversible alkali metal-CO2 batteries.

Catalyst‐Green Solvent System for Highly Efficient Production of Carboxylic Acids from Light Oxygenates, CO2 and H2

AbstractCatalytic hydrogenation of carbon dioxide (CO2) for the preparation of higher carboxylic acids is attractive and promising. Herein, we demonstrate a general strategy for producing higher carboxylic acids via reaction of CO2 and H2 with light (C2~C4) oxygenates such as ketones, alcohols, polyols, ethers and epoxides. In a green solvent consisting of ionic liquid (1‐ethyl‐3‐methylimidazolium iodide) and water, the reaction can be efficiently accelerated by RhI3 catalyst and I2 promoter at 170 °C. Very high or remarkable yields of higher carboxylic acids were synthesized via C−C bond formation between the intermediates generated from the oxygenates and CO2. Detailed study indicated that the catalyst and the solvent had excellent synergistic effect for promoting the reaction. The strategy can effectively convert the bulk and inexpensive feedstocks to value‐added carboxylic acids, and therefore is promising for commercial application.

The self-assembly of tetranuclear [Gd4] cluster: Magnetic refrigeration and efficient CO2 chemical fixation

In this paper, the self-assembly of Gd3+ ions and ligand 5-chlorine-8-hydroxylquinoline (HL) successfully generated one tetranuclear lanthanide compound [Gd4(µ3-OH)2(L)6(acac)4] (1) (L = 5-chlorine-8-hydroxylquinoline; Hacac = acetylacetone), in which four Gd3+ ions are connected into a [Gd4O2] cluster. Magnetic studies revealed that anti-ferromagnetic interactions between neighbouring Gd3+ ions were observed in 1. In addition, 1 also shows magnetocaloric effect and the −ΔSm value reaches 28.05 J kg−1 K−1 at T = 2.0 K and ΔH = 7 T. Catalytic experiments indicated that 1 and tetra-n-butylammonium bromide (TBAB) could synergistically catalyze the cycloaddition reaction of CO2 and epoxides at relatively mild condition.

Optimizing in-situ CO2 mineralisation: geomechanics and scalability in dunite and serpentinite rocks – Examples from Australia and New Zealand

The collective drive towards achieving net-zero greenhouse gas emissions by 2050 has spurred interest in engineering solutions for carbon capture and storage worldwide. One such approach involves the permanent storage of CO2 in earth-abundant Ca-, Fe-, and Mg-bearing silicate rocks and minerals as carbonates via the process of CO2 mineralisation. This necessitates a thorough understanding of carbonate conversion under geologically relevant conditions. Nevertheless, research on CO2 injection for mineralisation via naturally fractured host rocks or induced fractures, with a research emphasis on rock mechanics and stimulated reservoir volumes (SRV) within geoengineering CO2 storage, is continuously expanding. This research addresses critical challenges related to identifying favourable geographic locations for CO2 mineralisation. It specifically focuses on the abundant availability of Mg, Ca, and Fe cations for exothermic CO2 reactions and their impact on fracture conductivity during in-situ mineralisation. A comprehensive analysis of 26 dunite and serpentinite samples from diverse locations in Australia and New Zealand, including 10 from a cored drilled hole, was conducted. Quantification of divalent cation (Mg, Ca, Fe) content and cation release capacity using XRF and XRD revealed higher cation percentages in dunite samples (approximately 30 %) compared to serpentinite samples (approximately 26 %). Additionally, the study estimated the stimulated rock mass-to-CO2 sequestered ratio, RCO2, with dunite samples averaging approximately 2.20 RCO2 values and serpentinite samples averaging approximately 2.53. Geomechanical testing enabled the prediction of fracture propagation pressures during aqueous CO2 injection for in-situ mineralisation and the estimation of fracture geometries, emphasizing the role of rock stiffness in determining fracture width (averaging 6.0 mm). Furthermore, the research estimated the rock volume exposed to CO2-laden fluid during injection, particularly focusing on the GHQ-3 sample, which theoretically amounted to approximately 600 kg of rock capable of sequestering around 300 kg of CO2 for a 10 m3 fluid volume with a CO2 concentration of 1molkg−1. The study established a relationship between injected volume and CO2 uptake, suggesting the potential for significant CO2 sequestration scalability by employing horizontal wells and fracturing additional zones, thereby creating and intersecting multiple transverse fractures along a single target zone.

CO-PROX on MnO2 catalysts: DFT-based microkinetic and experimental macrokinetic approaches

A microkinetic analysis in terms of DFT-calculated temperature-dependent Gibbs free energies was performed for the oxidation reactions of CO and H2 on a model Mn4O8 cluster. Apparent activation energies data predict a peculiar CO preferential oxidation pattern of Mn(IV) sites in presence of hydrogen (PROX) substantiated by the unprecedented PROX behavior of a nanocomposite MnCeOx catalyst in the range of 353–423 K under both ideal and real process conditions. Micro- and macrokinetic data on the “model” cluster and “real” catalyst are discussed.

Design of New Bis(1,2,3-triazol-1-yl)methane-Based Nitrogen Ligands: Synthesis and Coordination Chemistry.

The reaction between bis(1,2,3-triazol-1-yl)methane derivatives and nBuLi and various aldehydes, yielded novel neutral ligand precursors incorporating alcohol functional groups. The resulting compounds exhibited distinct characteristics depending on the steric hindrance of the aldehyde employed. In instances where aromatic aldehydes were utilized, functionalization occurred at the methine group bridging both triazole rings. Conversely, the use of pivalic aldehyde prompted functionalization at the C5 position of the triazole ring. These compounds were subsequently employed as ligand precursors in the synthesis of organometallic aluminum and zinc complexes, yielding dinuclear complexes with high efficiency. The structural elucidation of all compounds was accomplished through spectroscopic methods and validated by X-ray crystallography. Preliminary catalytic investigations into the coupling reaction of cyclohexene oxide and CO2 revealed that aluminum and zinc complexes catalyzed the selective formation of polyether and polycarbonate materials, respectively.

Mechanistic insight into the C1 product selectivity for the catalytic hydrogenation of CO2 over metal-doped graphene

The conversion of CO2 into fuels and valuable chemicals presents a viable path toward carbon neutrality. The aim of this study is to investigate the potential of metal-doped graphene catalysts in the reduction of CO2 to C1 products. 20 typical M-graphene (M = metal) catalysts were established based on DFT calculations. Six candidate catalysts, i.e., V-, Cr-, Mn-, Ni-, Mo-, and Ta-graphene catalysts, were selected by combining the hydrogen dissociation ability and the energy band gap of the catalysts. Subsequently, the adsorption characteristics and hydrogenation reactions of CO2 over the six candidates were explored. CO2 tends to adsorb at the M site through vertical adsorption and carbon–oxygen co-adsorption. V- and Cr-graphene catalysts promote the production of intermediate COOH, whereas Mn-, Ni-, Mo-, and Ta-doped surfaces are more favorable for HCOO formation. Concerning the hydrogenation to CO and HCOOH, V-, Cr-, Ni- and Mo-graphene catalysts preferentially yield CO from COOH, whereas Ta-doped graphene favors the formation of HCOOH. In total, the competitive hydrogenation of CO2 reveals the selectivity of the C1 products. Cr- and Ni-graphene favor the production of HCOOH and CH3OH, whereas V-, Mn-, Mo-, and Ta-graphene primarily yield CH3OH.Graphical

Role of partial stable stratification on fluid flow and heat transfer in rotating thermal convection

The liquid iron core of the Earth undergoes vigorous convection driven by thermal and compositional buoyancy. The dynamics of convective fluid motions and heat transfer in such conditions are determined by background rotation, geometrical symmetry, and thermal interactions across the boundaries. In this study, rotating thermal convection in a horizontal fluid layer is considered to understand the fluid flow characteristics in the Earth's outer core focusing on the regions close to the rotational axis. The effects of a partial stable stratification on fluid flow and heat transfer are investigated to ascertain the physical significance of thermal core–mantle interaction on geomagnetic field generation driven by core fluid motion. It is found that even with non-linear evolution, convective instabilities retain the fundamental characteristics of linear onset modes. Mildly supercritical regimes lead to near laminar flows with the transition to turbulent convection occurring for strongly driven convection around 50–100 times enhanced buoyancy. Axial symmetry breaking and preferential damping of small-scale vortical structures are the hallmark of penetrative convection. Rapid rotation sustains small-scale helical flows in stable regions, a necessary ingredient for the sustenance of Earthlike dipolar magnetic fields. Coherent flow structures for strongly turbulent convection are obtained using reduced-order modeling. The overall total heat transfer is suppressed (up to 25%) due to the stable stratification although convective efficiency is enhanced (up to 30%) in the unstable regions favored by rapid rotation. Flow suppression is overcome under strong buoyancy forces, a relevant dynamical regime for deep-seated dynamo action in the Earth's core.

Enhancing CO and H2 Production in Propane Dry Reforming in Excess of CO2.

This study focuses on addressing the challenges in the dry reforming of propane, a process historically marked by low syngas yields and only moderate conversions of CO2 and propane. The primary objective was to enhance CO2 utilization and boost the selectivity of syngas (CO and H2) production using titania-based catalysts. For synthesizing these catalysts, an impregnation method was employed with subsequent characterization through X-ray diffraction (XRD), N2 adsorption-desorption, ammonia temperature-programmed desorption (TPD), and hydrogen temperature-programmed reduction (TPR). The titania-based catalysts generally possess weak acidic strength, with each catalyst displaying a unique reduction profile. The dry reforming process using these catalysts resulted in varying levels of propane conversion, with V/Ti, Ir/Ti, Al/Ti, and Zr/Ti catalysts showing distinct efficiencies. Notably, the Ir/Ti and V/Ti oxide catalysts achieved the lowest selectivity for generating intermediate byproducts such as methane, ethane, ethylene, and propylene while successfully promoting higher syngas CO and H2 production alongside stable propane conversion. When exposed to excess CO2, each catalyst consumed differing amounts of CO2 molecules. Particularly, the Ir/Ti and V/Ti oxide catalysts demonstrated enhanced activity in promoting CO2 reactions with intermediate radical species, facilitating carbon-carbon (C-C) bond dissociation and leading to increased syngas production. This study offers valuable insights into the potential of titania-based catalysts in improving the efficiency and selectivity of propane dry reforming processes for blue hydrogen.