Wide Range Of Pressures Research Articles

In Silico-Directed Design and Experimental Validation of an IL/UiO-66 Nanocomposite with Exceptional CO2 Selectivity across a Wide Pressure Range

In Silico-Directed Design and Experimental Validation of an IL/UiO-66 Nanocomposite with Exceptional CO₂ Selectivity across a Wide Pressure Range

Tunable soft pressure sensors based on magnetic coupling mediated by hyperelastic materials

Recent advances in pressure sensors have garnered significant interest due to their promising applications in healthcare, robotics and wearable technology. In these fields, there is an ever-increasing demand for soft sensors that can conform to complex surfaces, such as the human body. However, current sensors often face limitations in measurable pressure ranges and customization involves complex manufacturing processes. In this study, we introduce an innovative solution for producing soft pressure sensors with varying maximum detection pressures. By utilizing a magnetic transduction mechanism and different hyperelastic materials, we have developed sensors that can adapt to irregular surfaces. These sensors measure a wide range of pressures, from ultra-low to medium, and offer variable stiffness, sensitivity, and measurement ranges. The sensors we manufactured exhibit a detection range from 6.8 to 77.4 kPa, a sensitivity range between -5.1 × 10-2 and -0.4 × 10-2 kPa-1, a short recovery time of 0.4 s, low hysteresis values during repeated loading/unloading cycles, and stable response over thousands of pressure cycle. Proof-of-concept experiments validated the sensors’ suitability for breathing monitoring and finger tap detection, highlighting their potential in medical and robotic applications. The results demonstrate a robust strategy for controlling the performance of soft pressure sensors, positioning them as promising candidates for diverse pressure sensing applications.

Insight into the Kinetics of Isomerization and β-Scission Reactions Following H-Abstraction in 2-Pentanone Combustion.

2-Pentanone is a significant carbon-neutral fuel. To better understand 2-pentanone combustion, the CCSD(T)/CBS method was used to calculate the potential energy surfaces (PES) for H-abstraction, isomerization, and β-scission reactions of 2-pentanone. Rate constants for the above reactions were calculated by the MESS employing conventional transition state theory (CTST) at 300-2000 K. The findings reveal adherence to the Evans-Polanyi principle in the H-abstraction reactions of 2-pentanone by H atoms. Specifically, the 2-site shows more competitive kinetics due to having the lowest energy barrier of 7.8 kcal/mol. The 4-position has the highest energy barrier, making the reaction difficult to occur. In the subsequent reactions, the breaking of C-H bonds is most competitive at low temperatures. In particular, the H transfer from INT1 to INT3 has a potential well height of 24.8 kcal/mol. The β-scission reactions become the main pathway for the depletion of pentanone radicals with increasing temperature. This study significantly extends the kinetic parameters of 2-pentanone combustion over a wide range of temperatures and pressures, which is expected to contribute to the development of 2-pentanone combustion models.

Pressure and temperature diagram of C60 from atomistic simulations.

Although widely studied experimentally in the 1990s, the structure and properties of low-dimensional or high-pressure phases of fullerenes have recently been re-examined. Remarkably, recent experiments have shown that transparent, nearly pure amorphous sp3-bonded carbon phases can be obtained by heating a C60 molecular crystal at a high pressure. With the additional aim of testing the ability of three classical carbon potentials reactive empirical bond order, environment-dependent interatomic potential, and reactive force-field to reproduce these results, we investigate the details of the structural transformations undergone by fullerene crystals over a wide range of pressures and temperatures. All the potentials tested show that the initial polymerization of fullerenes is accompanied by negative thermal expansion, albeit in slightly different ranges. However, more significant differences in structural and mechanical properties are observed in the amorphous phases, in particular the sp3 carbon fraction and the existence of layered amorphous carbon. Overall, these results indicate to which extent classical reactive potentials can be used to explore phase transitions over a wide range of pressures and temperatures.

Effect of Mechanical Pressure on Rate Capability, Lifetime, and Expansion in Multilayer Pouch Cells with Silicon-Dominant Anodes

Microscale silicon particles have a higher specific capacity but larger volume expansion than graphite particles, leading to particle decoupling and lifetime limitations. This study investigates a wide range of external mechanical pressures from zero (ZP - 0.00 MPa) to high (HP - 0.50 MPa) pressure to determine the optimal pressure for high rate capability, cyclic lifetime, energy density, low temperature rise, and low cell thickness gain. The cells are characterized by rate tests and impedance spectroscopy, and are aged until 70% state of health (SoH). The post-mortem analysis after 70% SoH and thickness measurements over 360 cycles in a compression test bench offer insights into the thickness gain. Electrochemical results reveal an immediate reduction in discharge capacity upon transitioning from normal pressure (NP - 0.20 MPa) to ZP, with NP and HP exhibiting superior performance over aging. The impedance was reduced initially and over aging for higher mechanical pressures, especially the cathode contact resistance, resulting in lower temperature rises during the rate tests. Overall, applying higher pressures reduced the anode and cell thickness gain. Moreover, the porosity decreased with increasing pressure, as determined by mercury intrusion porosimetry and pycnometer measurements. The increase of the anode mass correlates to the total charge throughput, which is pressure-dependent and the highest for NP.

Ab initio insight into the physical properties of new ferroelectric perovskite oxide materials XGeO3 (X = Sr, Ca)

The investigation of structural stability, electronic, mechanical, spontanous polarization, and thermodynamic properties of simple cubic perovskite oxides XGeO3 (X =Sr, Ca) has been performed through density functional theory as introduced in Wien2K code. The tolerence factor, Born criteria, and phonon dispersion confirm the stability and the formation of both materials in the ideal cubic structure. Additionally, the application of nmBJ approach in electronic properties shows an exceptional semiconducting aspect. The strain effect on spontaneous polarization of XGeO3 (X =Sr, Ca) perovskites presents an excellent ferroelectric behavior. The thermodynamic parameters such as volume, bulk modulus, thermal expansion coefficient, Debye temperature, Gibbs free energy, enthalpy, heat capacities, and Gruneisen, have been ¨ calculated and discussed with a wide range of pressures (0−20 GPa) and temperatures (0−1000 K). Based on the exceptional semiconducting nature and significant spontaneous polarization, the studied materials can be considered as ferroelectric materials, which make them as a suitable candidates in ferroelctric devices.

Ab initio chemical kinetics and shock-tube experimental study on nitrocyclohexane pyrolysis and combustion

Nitrocyclohexane (NCH) is a model nitroalkane compound with naphthenic structural groups for studying the combustion properties of nitro-based energetic fuels, and also demonstrates significant potential applications for advanced engines. However, accurate description of the detailed kinetic mechanisms for pyrolysis and combustion of NCH receives little attentions. Herein, the detailed pyrolysis and oxidation mechanism of NCH is studied by using quantum chemistry calculations and chemical kinetic theory. The potential energy surfaces of the CN bond dissociation reaction, HONO elimination reaction, abstraction reactions of NCH as well as the subsequent β-scission reactions are calculated using G4//M06–2X/6–311++G(d, p) method, which are subsequently employed for reaction rate constant computations via transition state theory (TST) and RRKM/master-equation (RRKM/ME) method. The ab initio chemical kinetic study results are used to develop a detailed kinetic mechanism to predict the pyrolysis experimental results of NCH, which are performed using a single-pulse shock tube (SPST). The SPST experiment is performed at pressure of 10 bar, temperature ranging from 1070 to 1560 K, reaction time of around 1.77 microsecond with fuel concentrations of 0.5 % diluted by Argon gas. The developed detailed kinetic mechanism exhibits reasonable prediction results of the pyrolysis product distributions together with literature ignition delay times across a wide range of temperature, pressure, and equivalence ratio conditions. Rate-of-production analysis is conducted to gain insight into the pyrolysis chemical kinetics of NCH. The present work should be valuable for the study of the combustion chemistry of nitro-alkane energetic fuels.

Effect of surface roughness on methane adsorption in shale organic nanopores from the perspective of molecular simulations

Understanding the shale gas adsorption behavior within organic nanopores is crucial for its development. The pore surfaces commonly exhibit random inherent roughness, which can significantly impact gas adsorption, while it’s still in debate about whether the roughness could enhance the gas adsorption or not. To clarify the underlying mechanisms of the effect of surface roughness, in this study, the Grand Canonical Monte Carlo and Molecular Dynamic simulations are used to investigate the methane adsorption in wrinkled graphene nanochannels with various roughness. The heterogeneity of the adsorption layer along the rough topology is described in detail. The adsorption is enhanced near the concave region and weakened near the convex region. Additionally, increased surface roughness shifts the gas molecules’ aggregation modes in the concave region from a gradual gradient to oscillatory “adsorption points”. We observe that wall roughness due to the wrinkle can enhance the adsorption amount overall, attributed to the increased surface area and the increased unit adsorption capacity due to potential energy overlap. However, the contributions of both factors differ under various pressure and roughness conditions. Then a new mathematical method to estimate the gas adsorption amounts is provided and aligns well with molecular simulation results for a wide range of pressure and roughness conditions. And a potential answer the current debate about the positive or negative impact of adsorption due to roughness is promoted. The key may lie in the dominant role of the co-existed roughness caused by the fragment basal or edge surface. Our work could shed light on the underlying effect of surface roughness on the gas adsorption in shale, and have significant implications for the reserve estimation of shale gas formations.

A polynomial temperature profile model for suspended droplet evaporation over a wide range of ambient pressures and convection conditions

The suspended droplet technique has been widely applied in experimental droplet evaporation studies, but heat conduction caused by support fiber can change the evaporation characteristics. In the present study, a novel theoretical model is proposed to investigate the effect of a suspender on droplet heating and evaporation. Considering the vortex circulation inside the droplet and the heat diffusion along the support fiber, the temperature distribution is assumed to exhibit a polynomial profile. The effects of pressure on the thermodynamic and transport properties are also accounted for. The simulation results are consistent with previous experimental data over a wide range of ambient pressures and convection conditions. The performance of the new model is further compared with that of other models in terms of computational efficiency and accuracy. The new model requires an order of magnitude less CPU time than does the effective thermal conductivity model to preserve the key features of the temperature distribution accurately. In addition, a dual effect of the fiber diameter on the evaporation rate is demonstrated. With increasing fiber diameter, the evaporation rate increases and then decreases. There are two different patterns that can depict heat transfer between the suspended droplets and the fibers: an “immersed area pattern” and a “fiber temperature pattern”. A switchover in the two patterns is responsible for the dual effect, which occurs at a threshold fiber diameter related to the environment.

Understanding fluid dynamics and renal perfusion in acute kidney injury management.

Acute kidney injury (AKI) is associated with an increased risk of morbidity, mortality, and healthcare expenditure, posing a major challenge in clinical practice, and affecting about 50% of patients in the intensive care unit (ICU), particularly the elderly and those with pre-existing chronic comorbidities. In health, intra-renal blood flow is maintained and auto-regulated within a wide range of renal perfusion pressures (60-100 mmHg), mediated predominantly through changes in pre-glomerular vascular tone of the afferent arteriole in response to changes of the intratubular NaCl concentration, i.e. tubuloglomerular feedback. Several neurohormonal processes contribute to regulation of the renal microcirculation, including the sympathetic nervous system, vasodilators such as nitric oxide and prostaglandin E2, and vasoconstrictors such as endothelin, angiotensin II and adenosine. The most common risk factors for AKI include volume depletion, haemodynamic instability, inflammation, nephrotoxic exposure and mitochondrial dysfunction. Fluid management is an essential component of AKI prevention and management. While traditional approaches emphasize fluid resuscitation to ensure renal perfusion, recent evidence urges caution against excessive fluid administration, given AKI patients' susceptibility to volume overload. This review examines the main characteristics of AKI in ICU patients and provides guidance on fluid management, use of biomarkers, and pharmacological strategies.

Model for predicting oil testing fluid rheological parameters of Bohai Bay oilfield in wide temperature and pressure range

The rheological parameters of oil testing fluids play a crucial role in safely conducting oil testing operations, protecting reservoirs, and maintaining wellbore integrity, which are greatly influenced by temperature and pressure. This article conducted rheological experiments on commonly used potassium salt polymer systems and organic salt systems for oil testing fluids in the Bohai Bay Oilfield under 4–200 °C and 30–150 MPa. The experiments revealed the variation of rheological parameters with temperature and pressure. Nine commonly used rheological models were evaluated for their applicability to the two types of oil testing fluids. It was found that the Ross model was suitable for the potassium salt polymer system, while the power-law model was suitable for organic salt oil testing fluids. A new rheological parameter prediction model suitable for wide range of temperature and pressure and different testing fluid systems was proposed based on the optimized results. The average error for the potassium salt polymer system for oil testing fluids was 0.101%, and the error for the organic salt system for oil testing fluids was 0.113%. Both were superior to known rheological models and can meet the requirements of oil testing operations within the wide temperature and pressure range in the Bohai Bay Oilfield.

Evaluation of the ecological quality of the macroalgal communities along the Algerian coast (Algeria, Mediterranean Sea)

The assessment and preservation of the marine environment, particularly coastal ecosystems, has emerged as a global priority. In this study, the rocky bottom quality (CFR) index, which is based on macroalgae composition and abundance, was used to assess the ecological quality of coastal waters at six sites along the Algerian coast that represent a wide range of anthropogenic pressures. The sensitivity of the CFR index to the anthropogenic pressure index (MALUSI) was also assessed. Multivariate analyses (DCA, nMDS, cluster, SIMPER, and PCA) were used to assess the variability of macroalgal community structure. The CFR index calculated for this study was compared to the EEI-c and CARLIT indices. The CFR index classified the study sites based on ecological quality: good to high quality in the western sites (Ténès, Kouali1, and Kouali2) and moderate quality in the central sites (Fontaine, Fort de l’eau, and Surcouf). The findings indicate that the CFR and MALUSI indices are highly correlated. The abundance and composition of macroalgal communities are useful indicators of rocky shore quality, as demonstrated by structural analyses of characteristic macroalgae and opportunistic species. The competitive characteristic macroalgae of the Cystoseira sensu lato species were found to be associated with sites of good and high ecological quality. Stress-tolerant characteristic macroalgae (Pachymeniopsis lanceolata, Ellisolandia elongata, and Halopteris scoparia) and opportunistic ruderal species (Ulva rigida, Ulva lactuca, and Ulva linza) were found in sites with moderate ecological quality. The CFR index was compared with the EEI-c and CARLIT indices, and it can be noted that the three indices use different spatial scales, biological levels and species classifications. Therefore, CFR, EEI-c, and CARLIT indices are useful tools for assessing the quality of coastal waters.

Multimodal Intelligent Flooring System for Advanced Smart-Building Monitoring and Interactions.

The floor constitutes one of the largest areas within a building with which users interact most frequently in daily activities. Employing floor sensors is vital for smart-building digital twins, wherein triboelectric nanogenerators demonstrate wide application potential due to their good performance and self-powering characteristics. However, their sensing stability, reliability, and multimodality require further enhancement to meet the rapidly evolving demands. Thus, this work introduces a multimodal intelligent flooring system, implementing a 4× 4 floor array for multimodal information detection (including position, pressure, material, user identity, and activity) and human-machine interactions. The floor unit incorporates a hybrid structure of triboelectric pressure sensors and a top-surface material sensor, facilitating linear and enhanced sensitivity across a wide pressure range (0-800 N), alongside the material recognition capability. The floor array is implemented by an advanced output-ratio method with minimalist output channels, which is insensitive to environmental factors such as humidity and temperature. In addition to multimodal sensing, energy harvesting is co-designed with the pressure sensors for scavenging waste energy to power smart-building sensor nodes. This developed flooring system enables multimodal sensing, energy harvesting, and smart-sport interactions in smart buildings, greatly expanding the floor sensing scenarios and applications.

Kinetics of Water Adsorption in Metal-Organic Framework(MOF-303) for Adsorption Cooling Application

Adsorption cooling systems (ACS) powered by low-temperature heat offer an energy-efficient and environmentally friendly alternative to traditional vapor-compression systems. The effectiveness of ACS is significantly influenced by the alignment of the adsorbent properties with the operating conditions of the cycle. Metal-Organic Frameworks (MOFs) are considered the next generation of water harvesting and ACS. Many MOFs are synthesized and tested for water harvesting systems, one of these MOFs is MOF-303 which was reported to have very rapid water sorption dynamics under atmospheric conditions. However, MOF-303 has never been tested under the same conditions as ACS (under vacuum). In this study, the isotherms and kinetics of water adsorption on MOF-303, as an efficient adsorbent of water vapor, is experimentally investigated for the ACS using the linear driving force model. The diffusion coefficients across a wide range of relative pressures under two different temperatures were estimated. The study compares the adsorption process of MOF-303 with traditional silica gel (SG) in the context of diffusion kinetics relevant to ACS. Based on the output and at a constant temperature of 25 °C and across all relative pressure ranges, MOF-303 exhibited an average increase of approximately eight times in diffusion kinetics compared to SG. Specifically, within the relative pressure range of 10–30 %, which is optimal for ACS, MOF-303 demonstrated a seven-fold increase in diffusion kinetics over SG. The diffusion values for SG display a clear upward trend with increasing temperature. In contrast, the diffusion values for MOF-303 are subject to fluctuations with temperature changes under investigation. Notably, the isotherm for MOF-303 shows an inflection point at relative pressures between 10–15 %, causing a significant reduction in diffusion at these specific relative pressures compared to other relative pressure values. The findings in this study highlight the potential use of MOF-303 as a highly efficient water adsorbent for the ACS which will enable scientists and engineers to develop sustainable low-grade energy systems.

Water and Carbon Dioxide Capillary Bridges in Nanoscale Slit Pores: Effects of Temperature, Pressure, and Salt Concentration on the Water Contact Angle.

We perform molecular dynamics (MD) simulations of a nanoscale water capillary bridge (WCB) surrounded by carbon dioxide over a wide range of temperatures and pressures (T = 280-400 K and carbon dioxide pressures ≈ 0-80 MPa). The water-carbon dioxide system is confined by two parallel silica-based surfaces (hydroxylated β-cristobalite) separated by h = 5 nm. The aim of this work is to study the WCB contact angle (θc) as a function of T and . Our simulations indicate that θc varies weakly with temperature and pressure: Δθc ≈ 10-20° for increasing from ≈0 to 80 MPa (T = 320 K); Δθc ≈ -10° for T increasing from 320 to 360 K (with a fixed amount of carbon dioxide). Interestingly, at all conditions studied, a thin film of water (1-2 water layers-thick) forms under the carbon dioxide volume. Our MD simulations suggest that this is due to the enhanced ability of water, relative to carbon dioxide, to form hydrogen-bonds with the walls. We also study the effects of adding salt (NaCl) to the WCB and corresponding θc. It is found that at the salt concentrations studied (mole fractions xNa = xCl = 3.50, 9.81%), the NaCl forms a large crystallite within the WCB with the ions avoiding the water-carbon dioxide interface and the walls surface. This results in θc being insensitive to the presence of NaCl.

Trace element partitioning in a deep magma ocean and the origin of the Hf-Nd mantle array.

Crystallization in Earth's deep magma ocean could have caused trace element fractionation in the lower mantle that might be inherited to the isotopic compositions of the present-day mantle. However, the trace element partitioning has been experimentally investigated only up to the uppermost lower-mantle pressures. Here, we determined the bridgmanite/melt partition coefficients D of La, Nd, Sm, Lu, and Hf from 24 to 115 gigapascals, covering the wide pressure range of the lower mantle. Results demonstrate substantial reductions in DLu and DHf from >1 to ≪1 with increasing pressure to 91 gigapascals. We also found DLu/DHf > 1 and DSm/DNd < 1 under deep lower-mantle conditions, evolving melts toward low Lu/Hf and high Sm/Nd ratios by crystallizing bridgmanite. If residual melts form a dense hidden reservoir in the lowermost mantle, the complementary accessible mantle has the Hf and Nd isotopic compositions matching the observed terrestrial mantle array that deviates from the bulk silicate Earth reference.

Predicting phase coexistence and adsorption isotherms of classical and quantum fluids using the microcanonical-ensemble perturbation theory (MEPT)

The Microcanonical-Ensemble Perturbation Theory (MEPT) of Sastre et al. (2018) [7] has been extended to study the vapor-liquid phase coexistence of binary and ternary mixtures of fluids. The attractive interactions between chains of molecules are represented as monomer segments interacting via a square-well pair potential. Calculations for the thermodynamic properties and phase behavior of square-well monomer chains are considered and compared with experimental data. Molecular parameters have been obtained to model the phase behavior of real fluids such as n-alkanes (from C1 to C12), nitrogen, perfluoromethane, carbon dioxide, i-butane, i-pentane, neon, and hydrogen. Furthermore, the capability of the MEPT approach in predicting critical and azeotropic lines of binary and ternary mixtures is explored. The results demonstrate that the MEPT approach provides a robust description of the phase behavior of mixtures containing chains of fluids. Additionally, we have integrated the MEPT approach with the two-dimensional Statistical Associating Fluid Theory for fluids interacting via variable range potentials (SAFT-VR-2D) to investigate the effect of quantum contributions on both phase behavior and adsorption. Remarkable improvements are observed when both higher order perturbation terms of the Helmholtz free energy and quantum contributions are included in the predictions of the phase behavior of quantum fluids such as neon and hydrogen. In all cases, the theoretical results exhibit favorable comparisons with experimental data in a wide range of compositions, pressures, and temperatures.

Measurements of diffusion coefficient and kinetic diameter of acetone vapor via molecular tagging

The Molecular Tagging (MT) technique is a promising methodology for locally measuring velocity and temperature fields in rarefied gas flows. Recently, Molecular Tagging Velocimetry (MTV) has been successfully applied to gas flows in mini-channels in the continuum regime at high pressure and early slip-flow regime at lower pressure. As the operating pressure decreases, diffusion effects become more pronounced, and in MTV, they hinder the extraction of the correct velocity profile by simply dividing the displacement profile of the tagged molecular line by time of flight. To address this issue, a reconstruction method that considers Taylor dispersion was previously developed to extract the velocity profile, considering the diffusion effects of the tracer molecules within the carrier gas. This reconstruction method successfully extracted the correct velocity profile in the continuum flow regime. However, the method still faces challenges in the slip-flow regime. Since there is currently no consensus in the literature regarding the kinetic diameter value of acetone vapor, the diffusion coefficient estimation is uncertain especially at low pressures. This is why, in this study, we propose an original optical method to measure the diffusion coefficient of acetone vapor. This is achieved by linking the temporal evolution of the spatial photoluminescence distribution of acetone vapor to the diffusion coefficient via the Chapman-Enskog theory. Our research provides measurements of these parameters for a wide range of pressures (0.5–10 kPa) at ambient temperature.

Simulation of the THF hydrate-water interfacial free energy from computer simulation.

In this work, the tetrahydrofuran (THF) hydrate-water interfacial free energy is determined at 500 bar, at one point of the univariant two-phase coexistence line of the THF hydrate, by molecular dynamics simulation. The mold integration-host methodology, an extension of the original mold integration technique to deal with hydrate-fluid interfaces, is used to calculate the interfacial energy. Water is described using the well-known TIP4P/Ice model, and THF is described using a rigid version of the TraPPE model. We have recently used the combination of these two models to accurately describe the univariant two-phase dissociation line of the THF hydrate in a wide range of pressures from computer simulation [Algaba et al., J. Chem. Phys. 160, 164718 (2024)]. The THF hydrate-water interfacial free energy predicted in this work is compared with the only experimental data available in the literature. The value obtained, 27(2) mJ/m2, is in excellent agreement with the experimental data taken from the literature, 24(8) mJ/m2. To the best of our knowledge, this is the first time that the THF hydrate-water interfacial free energy is predicted from computer simulation. This work confirms that the mold integration technique can be used with confidence to predict the solid-fluid interfaces of complex structures, including hydrates that exhibit sI and sII crystallographic structures.

CO2 solubility in aqueous solution of salts: Experimental study and thermodynamic modelling

AbstractThere are many economic obstacles and complex engineering problems associated with CO2 capture and storage in saline aquifers that need to be addressed. Overcoming such challenges requires precise knowledge on the fluid phase equilibria of CO2‐brine systems. Having accurate CO2 solubility data over a wide range of temperature and pressure can greatly assist in resolving these obstacles by improving the performance and accuracy of the thermodynamic modeling and subsequent CCS engineering success.CO2 solubility in pure water and NaCl solutions has been widely studied in the literature, however, there is a lack of data on CO2 solubility at lower temperatures (below 298 K). Furthermore, limited phase equilibria data are available for CO2 solubility in CaCl2, MgCl2, and KCl solutions at elevated temperatures (i.e., T &gt; 323.15 K).In this work, the phase equilibria of CO2 and brine systems are investigated experimentally and theoretically. In this study, solubilities of CO2 in pure water and various concentrations of NaCl (10, 15, 20, and 22 wt%), KCl (10, 15, and 22 wt%), CaCl2 (7.5, 10, 15.7, and 23.4 wt%), and MgCl2 (6.7, 11, 18, and 29 wt%) aqueous solutions are reported. All CO2 solubilities were measures at 323.15, 373.15, and 423.15 K and over various pressure ranges, while solubilities in 10 and 20 wt% NaCl aqueous solutions were also measured over the temperature range of 263 to 298 K and pressures up to the hydrate dissociation pressure of each system. Equation of state modelling using the PC‐SAFT and the Cubic Plus Association equations of state, is performed in the theoretical part of the study to validate the measured solubility data. © 2024 The Author(s). Greenhouse Gases: Science and Technology published by Society of Chemical Industry and John Wiley &amp; Sons Ltd.