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Reducing greenhouse gas emissions or collecting and converting existing greenhouse gases has become a global concern. One of the most effective methods of utilizing CH4 and CO2 resources is the dry reforming of methane (DRM). Transition metal carbide catalysts have attracted wide attention because of their excellent catalysis performance and carbon deposition resistance. However, pure-phase carbides are easily oxidized and deactivated at atmospheric pressure in DRM reactions. There is a problem of poor dispersion (Mo2C 17 m² /g). Therefore, this paper summarizes the effects of adding active sites and supported carbides on the DRM reaction, discusses the role of active sites and supports in the catalyst, and introduces the different preparation methods of transition metal carbides. This paper also reviews the catalyst mechanism of transition metal carbides in DRM reactions. Nevertheless, the current research in this field needs to be deepened. Therefore, it is necessary to strengthen the exploration of various catalyst preparation methods and mechanisms, so as to realize future improvement in this field. [ABSTRACT FROM AUTHOR]

Global shale oil is abundant in geological reserves, but there are widespread problems of difficult exploitation and unsatisfactory oil recovery. CO 2 injection in shale reservoirs can achieve effective exploitation of shale reservoirs and alleviate the current energy shortage. In this paper, investigations on shale oil in recent years were summarized and analyzed. Firstly, the reservoir characteristics and fluid properties of several shale reservoirs and their effects on CO 2 -enhanced oil recovery (CO 2 -EOR) were analyzed, including porosity, permeability, mineral composition, pore structure, geomechanical characteristics and organic matter properties of shale reservoirs, as well as the density, viscosity, gas-oil ratio and composition of shale oil. Subsequently, multiple mechanisms of CO 2 -EOR in shale reservoirs were revealed, including swelling, diffusion, viscosity reduction, extraction, miscibility, and competitive adsorption. The effects of temperature, pressure, CO 2 injection amount, oil composition and reservoir heterogeneity on different mechanisms were analyzed. The effects of nanopore confinement and CO 2 injection on the fluid phase were also analyzed. Then, the CO 2 storage forms of structural space, bound space, dissolution, and mineralization were introduced. And the effects of temperature, pressure, reservoir heterogeneity and formation water salinity on various forms of CO 2 storage were summarized. Furthermore, the research methods of CO 2 injection technique through molecular simulation, physical simulation, mathematical model, and reservoir numerical simulation were introduced. Finally, the reasonable prospect of CO 2 injection technique for shale oil reservoirs was proposed based on the current technical problems. The purpose of this paper is to provide a theoretical basis for EOR and carbon geological storage of shale reservoirs by using the CO 2 injection technique. [Display omitted] • Reservoir and fluid properties of major shale oil reservoirs were summarized. • EOR mechanisms of CO2 injection in shale reservoirs were reviewed systematically. • Research methods of CO2 injection techniques in shale reservoirs were introduced. • Future perspectives of CO 2 injection techniques in shale reservoirs were analyzed. [ABSTRACT FROM AUTHOR]

Cement and concrete are essential for global development. However, cement manufacture is responsible for around 7–8% of global greenhouse gas emissions, with significant growth anticipated. Beyond efficiencies in cement manufacturing, other strategies for using less cement in construction through applying the principles of efficient design, circular economy and reuse also have the potential to reduce emissions. A further option is to move towards cements with different compositions and inherently lower embodied carbon dioxide. This paper focuses on these materials and the challenges to their widespread adoption, drawing mainly on applied research, trials and standardisation activities conducted in the UK and the EU. In addition to modification of standards, basic technical and practical information such as strength development curves, durability, site considerations and a shared broad body of evidence are key for specifiers to consider when using any new cement. The paper describes the role of standards and specifications and the underpinning information (applied research, published case studies and experience) essential in getting any new cement adopted. It also shows how a range of evidence from research and application can feed into a simple conceptual model and evidence base. [ABSTRACT FROM AUTHOR]

Strategies for changing the conductivity of Li 2 CO 3 is introduced into the fabrication of Li-CO 2 battery. Benefitting from the favorable hierarchical architecture constructed (CPM-MnO 2), facile charge transfer occurs between catalytic surface and Li 2 CO 3 by –OH⋯O hydrogen bonds improves the metallicity of Li 2 CO 3 , facilitating the formation/decomposition of Li 2 CO 3 and bestowing an ultra-long-term stability of 1087 cycles (4348 h). Taking into account its simplicity, scalable character and outstanding performance, this hierarchical composite electrode paves an effective trajectory for the future development of highly efficient cathodes for durable metal-CO 2 batteries. [Display omitted] • Excellent hierarchical structure of MXene and MnO 2 on carbon paper was fabricated. • Enriched charge transfer occurred on MXene and the MnO 2 by OH⋯O hydrogen bonding. • The prepared batteries showed an ultra-long cycle lifetime and low overpotential. • The optimized electronic structure can improve the metallicity of Li 2 CO 3. • The accelerated decomposition of discharge products promoted CRR and CER kinetics. Lithium-CO 2 batteries are recognized as an essential strategy for efficient carbon sequestration and energy storage to achieve carbon neutrality. Their cycle-ability and polarization voltage, however, are hindered by high decomposition voltage (≈4.3–4.5 V) of insulating Li 2 CO 3. Herein, we report a significant advance toward the rational design of self-supporting and ultra-long cycle lifetime cathode for Li-CO 2 batteries, dependence on a favorable hierarchical architecture and rich charge transfer constructed by homogeneously distributed MnO 2 nanoplates rooted in the MXene surface supported by carbon paper. Detailedly, it exhibits impressive ultra-long-term stability of 1087 cycles (4348 h) with a low polarization gap (≈ 0.47 V) at a high current of 200 μA cm−2, which is outperformed by all the liquid electrolyte-based Li-CO2 batteries reported previously. Electronic structure analysis reveals that facile charge transfer occurs between catalytic surface and Li 2 CO 3 , springing from the –OH functional group (in MXene) to MnO 2 by –OH⋯O hydrogen bonds, which acts as charge transfer channels, improving the metallicity of Li 2 CO 3 and facilitating its decomposition and extending battery cyclability. This work paves an effective trajectory for the future development of highly efficient cathodes for durable metal-CO 2 batteries. [ABSTRACT FROM AUTHOR]

Presents a study that investigated the biodegradability and disintegration of paper product and its effects on compost quality. Effect of lignin content of materials in the low biodegradability level based on microbial degradation and measurement of carbon dioxide evolution; Degradation of nylon bags; Results of data analysis.

This paper aims at the theoretical study of the CO2 magnetic-dipole ν2 + ν3 rovibrational absorption band that was recently detected in the Martian atmosphere. Specific characteristics of the magnetic dipole operator are carefully examined. Our evaluation of the magnetic-dipole line intensities is based on the variational calculations and the use of molecular properties is determined through specially performed ab initio quantum chemical calculations. The comparison of our simulated magnetic-dipole spectrum with available laboratory taken data also requires the knowledge of line intensities in the quadrupole band, which partially overlaps with that magnetic-dipole. Quadrupole intensities, once reconsidered, are permitted to correct previously reported values of the integrated intensity as well as the intensity of selected branches. The sum of our calculated magnetic-dipole and quadrupole rovibrational lines is shown to be in good agreement with both sets of presently available data from FTIR and OFCEAS laboratory observations. [ABSTRACT FROM AUTHOR]

Abstract: The objective of the present work was to understand how the structural, surface, water vapour and gas barrier properties of wheat gluten (WG) coated paper could be influenced by the features of paper. For this purpose, a surface treated paper (TP) and an untreated paper (UTP) were compared. Penetration of WG-coating into the bulk of paper was more pronounced in UTP than TP. This led to the formation of a significant junction zone resulting in an interpenetrated structure for WG–UTP, suggesting a composite-like structure, while a bi-layer one was obtained for WG–TP. Differences in WG penetration were related to the hydrophilicity, roughness and porosity of the paper used. Even though the extent of penetration did not greatly affect the surface properties (water and oil resistance), the transfer properties (water vapour, O2 and CO2) of WG-coated papers were significantly improved when WG-coating highly penetrated: while the WG–TP behaved as a micro-perforated material, the WG–UTP behaved as WG-film. [Copyright &y& Elsevier]

As a part of our research in the field of thermochemical energy storage, this study aims to investigate the potential of three fly ash samples derived from the fluidized bed reactors of three different pulp and paper plants in Austria for their use as thermochemical energy (TCES) and CO2 storage materials. The selected samples were analyzed by different physical and chemical analytical techniques such as X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), particle size distribution (PSD), scanning electron microscopy (SEM), inductively coupled plasma atomic emission spectroscopy (ICP-OES), and simultaneous thermal analysis (STA) under different atmospheres (N2, CO2, and H2O/CO2). To evaluate the environmental impact, leaching tests were also performed. The amount of CaO as a promising candidate for TCES was verified by XRF analysis, which was in the range of 25–63% (w/w). XRD results indicate that the CaO lies as free lime (3–32%), calcite (21–29%), and silicate in all fly ash samples. The results of STA show that all fly ash samples could fulfill the requirements for TCES (i.e., charging and discharging). A cycling stability test of three cycles was demonstrated for all samples which indicates a reduction of conversion in the first three reaction cycles. The energy content of the examined samples was up to 504 kJ/kg according to the STA results. More energy (~1090 kJ/kg) in the first discharging step in the CO2/H2O atmosphere could be released through two kinds of fly ash samples due to the already existing free lime (CaO) in those samples. The CO2 storage capacity of these fly ash samples ranged between 18 and 110 kg per ton of fly ash, based on the direct and dry method. The leaching tests showed that all heavy metals were below the limit values of the Austrian landfill ordinance. It is viable to say that the valorization of fly ash from the pulp and paper industries via TCES and CO2 storage is plausible. However, further investigations such as cycling stability improvement, system integration and a life cycle assessment (LCA) still need to be conducted. [ABSTRACT FROM AUTHOR]

This work proposes to utilize supercritical CO 2 as a reaction medium for the acetylation of Hanji, a traditional Korean cellulose textile, to enhance its water repellency while retaining the other properties. We first examined the phase behavior of acetic anhydride and CO 2 mixtures, then a series of experiments were performed and statistically analyzed to find optimal operating conditions. Good surface hydrophobicity was attained in the optimized process within 4 h, shorter than classical non-catalytic liquid and gaseous processes. Hanji's tensile strength was also enhanced in the proposed process by a factor of 1.1, while it was aggravated in classical liquid processes. Hanji samples were slightly discolored in the proposed method, but the degree of discoloration was below the perception level. These results suggest that the proposed method has great potential to be used for the functionalization of cellulose-based textiles with a wide range of industrial applications. [Display omitted] • ScCO 2 -mediated acetylation was optimized to enhance Hanji's surface hydrophobicity. • Surface hydrophobicity is improved in scCO 2 -mediated acetylation within 4 h. • Tensile index increases by 11% in scCO 2 -mediated acetylation. • Tensile index decreases by 20% in classical acetylation methods. • Cellulose discoloration in scCO 2 -mediated acetylation is mild. [ABSTRACT FROM AUTHOR]

The diffusion behaviour of hydrogen, carbon monoxide, carbon dioxide, methane, acetylene, ethylene and ethane in oil and paper medium was examined using molecular dynamics to reveal the diffusion mechanism of gas molecules in transformer oil–paper insulation system at the microscopic level. These compounds are commonly used in the dissolved gas analysis of power transformers and produced during the ageing process of oil–paper composite insulating material. Two groups of models were constructed using molecular dynamics simulation software to simulate the diffusion behaviour of the aforementioned seven types of small gas molecules in oil and paper. The diffusion coefficients, displacement features, free volume characteristics and interaction energies of the gas molecules were investigated. In particular, the diffusion micro-mechanism of the gas molecules was observed. The differences in diffusion features among the gas molecules were discussed, and the factors influencing the diffusion of the gas molecules were compared. Simulation results indicate that the diffusion coefficients of gas molecules in cellulose is an order of magnitude lower than that in oil, and the diffusion coefficients of these gas molecules in the two types of insulation media have different orders. Free volume of gas molecules is the main factor that influences the diffusion behaviour in oil, whereas intermolecular interaction is the main influencing factor of diffusion behaviour in cellulose. [ABSTRACT FROM PUBLISHER]

• Concentrations of atmospheric CO2 and tropospheric ozone (O3) are rising concurrently in the atmosphere, with potentially antagonistic effects on forest net primary production (NPP) and implications for terrestrial carbon sequestration. • Using free-air CO2 enrichment (FACE) technology, we exposed north-temperate forest communities to concentrations of CO2 and O3 predicted for the year 2050 for the first 7 yr of stand development. Site-specific allometric equations were applied to annual nondestructive growth measurements to estimate above- and below-ground biomass and NPP for each year of the experiment. • Relative to the control, elevated CO2 increased total biomass 25, 45 and 60% in the aspen, aspen–birch and aspen–maple communities, respectively. Tropospheric O3 caused 23, 13 and 14% reductions in total biomass relative to the control in the respective communities. Combined fumigation resulted in total biomass response of −7.8, +8.4 and +24.3% relative to the control in the aspen, aspen–birch and aspen–sugar maple communities, respectively. • These results indicate that exposure to even moderate levels of O3 significantly reduce the capacity of NPP to respond to elevated CO2 in some forests. [ABSTRACT FROM AUTHOR]

[Display omitted] This paper develops a new measurement method to answer the question: How does one measure the interfacial tension of adsorbed droplets? This measurement is based on the placement of a bubble at a water|organic interface. To prove the concept, a bubble was formed by pipetting gas below the water|1,2-dichloroethane interface. Our values agree well with previous reports. We then extended the measurement modality to a more difficult system: quantifying interfacial tension of 1,2-dichloroethane droplets adsorbed onto conductors. Carbon dioxide was generated in the aqueous phase from the electro-oxidation of oxalate. Given carbon dioxide's solubility in 1,2-dichloroethane, it partitions, a bubble nucleates, and the bubble can be seen by microscopy when driving the simultaneous oxidation of tris(bipyridine)ruthenium (II), a molecule that will interact with CO 2 .−. and provide light through electrochemiluminescence. We can quantify the interfacial tension of adsorbed droplets, a measurement very difficult performed with more usual techniques, by tracking the growth of the bubble and quantifying the bubble size at the time the bubble breaks through the aqueous|1,2-dichloroethane interface. We found that the interfacial tension of nanoliter 1,2-dichloroethane droplets adsorbed to an electrified interface in water, which was previously immeasurable with current techniques, was one order of magnitude less than the bulk system. [ABSTRACT FROM AUTHOR]

• CaCl 2 is an additive suitable for pyrometallurgical recovery of spent LIBs. • CaCl 2 has good chlorination ability and slag optimization ability. • SiO 2 and CO 2 in the system contribute to the increase in HCl yield. The difficulty of separating Li during pyrometallurgical smelting of spent lithium-ion batteries (LIBs) has limited the development of pyrometallurgical processes. Chlorination enables the conversion of Li from spent LIBs to the gas phase during the smelting process. In this paper, the effects of four solid chlorinating agents (KCl, NaCl, CaCl 2 and MgCl 2) on Li volatilization and metal (Co, Cu, Ni and Fe) recovery were investigated. The four solid chlorinating agents were systematically compared in terms of the direct chlorination capacities, indirect chlorination capacities, alloy physical losses and chemical losses in the slag. CaCl 2 was better suited for use as a solid chlorinating agent to promote Li volatilization due to its excellent results in these indexes. The temperature required for the release of HCl from MgCl 2 , facilitated by CO 2 and SiO 2 , was lower than 500 °C. The prematurely released HCl failed to participate in the chlorination reaction. This resulted in approximately 12 % less Li volatilization when MgCl 2 was used as a chlorinating agent compared to when CaCl 2 was used. In addition, the use of KCl as a chlorinating agent decreased the chemical dissolution loss of alloys in the slag. The performance of NaCl was mediocre. Finally, based on evaluations of the four indexes, recommendations for the selection and optimization of solid chlorinating agents were provided. [ABSTRACT FROM AUTHOR]

This paper conducts a computational investigation of the phase behaviour of $ \textrm{C}{\textrm{H}_4} $ C H 4 - $ \textrm{C}{\textrm{O}_2} $ C O 2 binary system, utilising the SAFT-VR Mie equation of state alongside molecular dynamics (MD) simulations. Molecular parameters for pure $ \textrm{C}{\textrm{H}_4} $ C H 4 and $ \textrm{C}{\textrm{O}_2} $ C O 2 compounds were obtained by fitting the SAFT-VR Mie EOS to vapour pressure and saturated liquid density experimental data. The research first validates the SAFT-VR Mie EOS on thermodynamic properties and vapour–liquid equilibria for different compositions, pressures, and temperatures of pure $ \textrm{C}{\textrm{H}_4} $ C H 4 , $ \textrm{C}{\textrm{O}_2} $ C O 2 , and $ \textrm{C}{\textrm{H}_4} $ C H 4 - $ \textrm{C}{\textrm{O}_2} $ C O 2 mixtures with the newly extracted parameters. The study confirms the EOS's accurate prediction of coexistence properties, including pressure, density, and phase-equilibrium curve. MD simulations were performed using the LAMMPS software package, with Mie force field parameters derived from this study for non-bonded interactions. Simulations were conducted using three other force fields (OPLS-UA, UFF, and GAFF) to compare their performance with our approach. The simulation results were compared to laboratory data, or REFPROP, in the absence of laboratory data. The results showed a relatively good agreement, indicating that combining SAFT-VR Mie EOS and MD simulations is a reliable predictive tool for designing gas processing and gas storage applications involving $ \textrm{C}{\textrm{H}_4} $ C H 4 - $ \textrm{C}{\textrm{O}_2} $ C O 2 mixtures. This approach also mitigates the need for expensive and hazardous high-pressure laboratory techniques. [ABSTRACT FROM AUTHOR]

• An enhanced ejector-subcooler CO 2 transcritical refrigeration cycle is presented. • A parametric analysis and optimization of the enhanced cycle and the baseline cycle are carried out. • The results suggest the integration of the proposed cycle could achieve more compact and reliable systems. • The maximum COP improvements are computed as 11.7%-17.5% when the gas cooler outlet temperature ranges from 35 °C to 50 °C and the evaporating temperature is -40 °C. The main drawback associated with CO 2 refrigeration systems is related to their performance reduction during transcritical operation at warm climate conditions, which may be compensated by better cycle architectures such as the split-cycle with subcooling or the flash-tank configuration, among others. Specifically, the use of standard gas-ejectors together with parallel compressors provides even better efficiency improvements, not being able to use them with low-temperature evaporators to prevent the triple point inside the ejector. This paper proposes an enhanced cycle with a gas ejector for two-stage compressor architectures with vapor injection from the flash-tank, which is able to operate at low evaporating temperatures and that provides a greater performance improvement the more severe the climate conditions are. The methodology conducted is based on a thermodynamic analysis that includes parametric evaluation and cycle optimization, comparing the results to a conventional CO 2 transcritical cycle with flash-tank and dynamic vapor injection architecture. The main results show that a maximum Coefficient of Performance improvement of 17.5% is achievable for transcritical operation at -40 °C evaporating temperature. The compressor displacement capacity required with the enhanced cycle is up to 9% lower for the same refrigeration demand, reducing the electrical consumption as well as the compressor expenditure. Moreover, greater vapor injection mass flow rates are obtained by the gas-ejector injection with discharge temperature reductions up to 18%, enhancing the system reliability. [ABSTRACT FROM AUTHOR]

• The zoning simulation method was developed for CO 2 ejector. • Comparison of different numerical models for each section. • The zoning simulation can predict entrainment ratio more accurately. • Effects of geometries on performances of ejector were analyzed. In this paper, a novel simulation method (zoning simulation) for the CO 2 ejector containing lubricant oil is established. Firstly, the feasibility of the zoning simulation method is verified. Subsequently, the phase change model and turbulence model are selected for each section when using the zoning simulation method. The average relative discrepancy of entrainment ratio using zoning simulation is 8.696%, and the average relative discrepancy of entrainment ratio using overall simulation is 14.118%. The results demonstrate that the predicted entrainment ratio using zoning simulation outperforms entrainment ratio using overall simulation. Introducing the concepts of relative temperature and relative pressure, the average relative discrepancy of entrainment ratio using zoning simulation is reduced to 4.620 %, when both relative temperature and relative pressure greater than 1. [ABSTRACT FROM AUTHOR]

A R744 (CO 2) refrigeration system has been designed to cool down the Large Hadron Collider (LHC) silicon detectors ATLAS and CMS, located at CERN, Switzerland. The silicon detectors are subjected to high radiation levels. The system is composed of a pri- mary CO 2 trans-critical booster vapor compression loop operated with piston compressors, and an oil-free liquid pumped loop on the evaporation side, to preserve the detectors. To ensure the system's reliability, the cooling facility is designed to operate under a parallel operation mode of several modular 70 kW plant units providing evaporation temperature as low as -53 °C. This layout, is also useful in case of components failure and maintenance. A numerical model is developed using a dynamic simulation software Dymola that is based on the open source Modelica modelling language. The simulation results are proven on a first demonstration plant (System A) experimentally to explore the systems control logic and to validate the reliability of the system before it is built on the detectors side. In this paper the models development is explained and the results of the experimental validation of the numerical model are shown. [ABSTRACT FROM AUTHOR]

• Ejector cycles achieved higher performance than booster cycle within the gas cooler outlet temperature range of 31 and 50°C. • Multi-ejectors can be applied to ejector cycles with different configurations. • Up to 17% annual energy consumption reduction was found using ejector cycles. • Unit product exergy costs of ejector cycles are up to 28% lower than booster cycle. Restrictions on high-GWP refrigerants have made the use of transcritical CO 2 refrigeration systems widespread. Using transcritical booster refrigeration cycle in warm climates is unsatisfactory due to its high energy consumption. This paper presents theoretical analysis and performance comparison of three different transcritical CO 2 supermarket refrigeration cycle configurations with ejector expansion in Türkiye, which has different climatic regions. Bin-hour data were derived using hourly dry-bulb temperature values for provinces from 7 different regions in Türkiye. The applicability of multi-ejectors to each modeled cycle was also investigated. Annual energy consumption and environmental impact reductions of up to 17% were obtained using ejector expansion cycle compared to booster cycle. Ejector expansion cycles achieved higher performance than booster cycle up to 46% in terms of exergy efficiency at investigated ambient temperatures. Unit product exergy costs of the ejector cycles were found up to 28% lower than booster cycle. [Display omitted] [ABSTRACT FROM AUTHOR]

Despite extensive works have been devoted to study the scale inhibition behavior, the performance of inhibitors is still not fully understood. In this paper, we present a laboratory study to elucidate the impact of water composition on the performance of some commonly used phosphonate and polymeric calcium carbonate scale inhibitors, in highly supersaturated brines at high temperature. Calcium tolerance inhibitor chemicals with various molecular structures are studied using dynamic scale loop test method at 150 °C. Brine composition is varied by changing the non-stoichiometry of scaling lattice ions, e.g., ( Ca 2 + ) / ( CO 3 2 − ) ratio, over a wide range. Test results indicate that the effectiveness of inhibitors can be significantly changed by the scaling ion ratio. In general, the efficacy of inhibitors decreases significantly with calcium concentration in the test brine even at constant supersaturation state and temperature, and also the performance ranking of the different inhibitor chemistries can be changed with brine composition. This could be caused by the alternations of interactions between inhibitor molecules and the surface of calcium carbonate scale crystals. Findings from this study suggest that the effect of scaling ion ratio must be considered in scaling risk assessment and for the optimization of inhibitor treatment programs. [ABSTRACT FROM AUTHOR]

The adverse effects of climate change calls for the rapid transformation of manufacturing processes to decrease the emissions of carbon dioxide. In particular, a lower carbon footprint can be achieved by capturing carbon dioxide at the site of emission. Here we review the use of industrial effluents, waste and residues to capture carbon dioxide. Waste include steelmaking slag, municipal solid waste incinerator ashes, combustion fly ash, black liquor, paper mill waste, mining waste, cement waste, construction and demolition waste, waste from the organic industry, and flue gas desulfurization gypsum waste. Capture capacities range from 2 to 800 kg of carbon dioxide per ton of waste, depending on processes, waste type and conditions. Cement waste and flue gas desulfurization gypsum waste show the highest capture capacity per ton of waste. [ABSTRACT FROM AUTHOR]

Abstract: In this study, experiments were conducted to investigate the applicability of low-cost alkaline paper mill wastes as acidity neutralizing agents for treatment of acid mine drainage (AMD). Paper wastes include a calcium mud by-product from kraft pulping, and a calcite powder from a previous study focused on sequestering CO2 by carbonation of calcium mud. The neutralization process consisted of increase of pH by alkaline additive dissolution, decrease of metals solubility and precipitation of gypsum and poorly crystallized Fe–Al oxy-hydroxides/oxy-hydroxysulphates, which acted as a sink for trace elements to that extent that solutions reached the pre-potability requirements of water for human consumption. This improvement was supported by geochemical modelling of solutions using PHREEQC software, and observations by scanning electron microscope and X-ray diffraction of reaction products. According to PHREEQC simulations, the annual amount of alkaline additive is able to treat AMD (pH 3.63, sulphate 3800mgL−1, iron 348mgL−1) with an average discharge of about 114 and 40Ls−1 for calcium mud and calcite powder, respectively. Likewise, given the high potential of calcium mud to sequester CO2 and of resulting calcite powder to neutralize AMD, paper wastes could be a promising solution for facing this double environmental problem. [Copyright &y& Elsevier]

Abstract: In this paper, the prospect of integrating a combined paper&pulp mill with fuel production via biomass gasification was investigated. In the study, three different types of gasifiers (circulating fluidised bed, entrained flow and indirect gasification) and three fuel processes (dimethyl ether, methanol and Fischer-Tropsch wax synthesis) were investigated using computer simulations. The paper reports differences from the stand-alone cases and the integrated cases, using the electricity equivalence efficiency as a measure. Only 6 out of the 18 integrated cases studied displayed a positive result from integration and no obvious fuel selection that stand out as the most beneficial one, however the synthesis of dimethyl ether is, in combination with all gasifiers assessed a rather good choice, with an change in efficiency from integration ranging from −1% to 4%. Dimethyl ether is not the best choice if the electrical equivalence is to be maximised however. In this case the combination of circulating fluidised bed gasification and methanol synthesis should be pursued. The production of Fischer-Tropsch wax should according to the chosen measure not be produced; however there is an added value in the production of a non-oxygenated fuel which has not been taken into account in this particular study. All cases leads to a reduction of 0.4–0.9 kg CO2 per kg of dry biomass used in the process for fuel synthesis and the possibility to export bark is a more significant factor in this respect than which type of fuel is synthesised. [Copyright &y& Elsevier]

With the assistance of digital pen and paper technology in the field of prehospital data reporting, it seems to be possible to fulfill the requirements of „documentation“ as well as the requirements of „quality management“. The aim of this study was to determine the „primary documentation quality“ (PDQ) of a data reporting system based on digital pen and paper technology (so-called DINO) within a helicopter emergency medical service (HEMS) over a 6-month period. The PDQ is defined as the proportion of prehospital documented data, which is primarily recorded correctly by the data reporting system. For the national uniform core dataset (so-called MIND2) the PDQ was 96.7%, for „checkbox“ and „numeric data fields“ the PDQ was 99.8% and 93.6%, respectively and for „vital data“ the PDQ was 96.7% [heart rate (HF), measurement of blood pressure] and 84.1% [peripheral oxygen saturation (SpO2), end tidal carbon dioxide concentration (etCO2), oxygen administration (O2)]. For „measurements“ the PDQ was 96.9% (time stamps) and 86.9% (time frames), for „drugs“ the PDQ was 43.6% (drug name) and 69.8% (drug dosage) and for“placement of infusion” 42% (infusion name) and 85.3% (infusion time), respectively. The average time for the „verification process“ after mission completion was 1.5±0.4 min/mission. The „primary documentation quality“ of prehospital mission data reporting with the assistance of a digital pen and paper based documentation system (DINO) has been shown to completely fulfill the requirements of rapid and safe data documentation in actual missions, even at this early stage of development. [ABSTRACT FROM AUTHOR]

Abstract: Inorganic fiber network including YSZ fiber which acts as catalyst support was created by the simple paper-making process, and novel Ni-loaded paper-structured catalysts (PSCs) with excellent catalytic activity for the dry reforming of methane were designed and developed. The PSCs exhibited high fuel conversion comparable to the conventional powdered catalysts with less than one-tenth catalyst weights. The significant advantages of the PSCs are their high mechanical flexibility and material workability. So far, a functionally-graded catalytic reaction field which leads to uniform temperature distribution during biogas reforming resulting in stable operation of planar SOFC was successfully developed by the PSC array based on the kinetic simulation model built in this research. [Copyright &y& Elsevier]

[Display omitted] • A bifunctional flexible Pt/TiO 2 -γ-Al 2 O 3 nanofiber paper was successfully prepared. • The PTA sample can efficiently decompose HCHO to CO 2 and H 2 O at room temperature. • PTA1 exhibited better catalytic activity and stability. • The surface coating of TiO 2 in PTA catalyst plays an important role for its performance. • The PTA sample also exhibits good filtration performance for fine particles. A flexible Pt/TiO 2 /γ-Al 2 O 3 nanfiber paper (PTA) was successfully prepared by an electrospinning-coating-NaBH 4 reduction method. The catalytic performance for formaldehyde (HCHO) oxidation over PTA with different Pt contents was investigated at room temperature. The results show that PTA exhibits higher catalytic activity and stability than Pt/γ-Al 2 O 3. The TiO 2 coating can promote the transformation of intermediate species and the desorption of CO 2. The PTA1 with 1 wt% Pt shows the best catalytic activity and good stability. In the view of activity and cost, 0.5 wt% Pt is the optimal Pt content. The TiO 2 coating not only plays an important role in improving the activity and stability of PTA, but also acts as a protective shell of γ-Al 2 O 3 fiber, which greatly reduces the risk of alkali etching during preparation and maintains the good flexibility of PTA. The dioxymethylene (DOM), formate/carbonate species, CO are the intermediate species in HCHO oxidation over PTA. In addition, PTA exhibits good filtration performance for fine particles as well as good fluid permeability. Because of the high efficiency and flexibility of PTA composite catalytic material for HCHO oxidation with good filtration performance for fine particles, it will be a promising candidate in air purification. [ABSTRACT FROM AUTHOR]

The reverse water gas shift (RWGS) is of great significance to the resource utilization of CO 2. In this paper, based on the features of MoO 3 , the Mo-based catalysts doped with Ga, Ti and Ce were prepared, and the effects of oxygen vacancies and basic sites on the RWGS reaction were studied. When the volume ratio of H 2 and CO 2 is 1 : 1, the yield of CO can reach 26.66%. Because it exposes higher concentration of Ce sites and moderate alkaline active sites on the surface. When the proportion of H 2 in the reaction gas increases, the highest yield of CO can reach 54.53%, which is mainly attributed to a large number of oxygen vacancies on the surface of MoTi. This study can be used as a reference for the design of catalysts for RWGS reaction under different reaction conditions. A series of Mo-based catalysts were prepared, and the significance of oxygen vacancies and surface basic sites in RWGS reaction was explored, and a reference was provided for the study of similar catalytic materials under different reaction gas ratios. [Display omitted] • MoO 3 by doping transition metal has a good application prospect in RWGS reaction. • The yield of MoTi and MoCe is close to equilibrium in RWGS reaction. • High CO 2 concentration is good for MoTi with higher density oxygen vacancies. • High H 2 concentration is good for MoCe with higher density surface basic sites. [ABSTRACT FROM AUTHOR]

The rapid depletion of fossil fuels has become the worst scenario as most of the energy needed still depends on the use of fossil energy, oil, natural gas, and coal. The combustion of crude oil and coal has contributed to the major anthropogenic carbon dioxide (CO 2) gas in the atmosphere and has worsened climate change and global warming. Therefore, the abundant CO 2 in the surrounding has opened the door to many studies to convert CO 2 into the next generation of fuels and indirectly reduce the greenhouse effect. Transition metal dichalcogenides (TMDs) nanomaterials have appeared as a practical and reliable catalyst for CO 2 conversion to sustainable fuels under normal atmospheric conditions. Having fascinating electronic and catalytic properties, these earth-abundant element-based materials are being explored and developed for real-world application. This paper reviews the recent insight into the synthesis, properties and application of TMDs as catalysts in electrocatalysis, photocatalysis and thermal catalysis for CO 2 reduction and conversion. The role of type of sulfide (S), selenide (Se) and telluride (Te)-based TMDs in the production of various valuable products such as formate (HCO 2 −), formic acid (CH 2 O 2), methanol (CH 3 OH), and ethanol (CH 3 CH 2 OH), amongst others, will be discussed in detail. The possible reaction pathways and mechanisms and the relationship between tailoring the catalysts properties and CO 2 activation towards high CO 2 reduction and conversion efficiency will also be evaluated. • TMD catalysts have demonstrated promising performance in converting CO 2. • TMD catalyst can be used for electro-, photo- and thermal-catalytic CO 2 conversion. • The synthesis and characterization methods of TMD catalysts has been reviewed. • The different types of TMD catalysts and their potential have been investigated. • The mechanisms of all catalytic reactions have been examined. [ABSTRACT FROM AUTHOR]

Most anthropogenic carbon dioxide (CO2) emissions originate from urban areas. To improve understandings of urban and regional emissions, we design and construct a low-cost UAV coordinated carbon observation network (LUCCN) which uses mid-accuracy (±1 ppm) CO2 sensors. In this paper, we introduce our multi-variable non-linear regression method for calibrating the non-dispersive infrared (NDIR) CO2 sensors for LUCCN's ground stations. We tested our calibration method with concentration data collected at the Xinglong Atmospheric Background Observatory. With comparison against data simultaneously collected by a high-accuracy cavity ring-down spectrometer, we found the maximum standard deviation of LUCCN's sensors to be 0.782 ppm in a controlled laboratory environment with a 1-second window size and 0.53 ppm in an outdoor environment with a 1-hour running average window size. As validation of LUCCN's ground measurements, we identify and present consistent trends between local CO2 concentration variations and aerosol pollution events captured by the space-based moderate resolution imaging spectrometer (MODIS). [ABSTRACT FROM AUTHOR]

Insufficient active sites at the hydrophilic grassy CuO electrode tend to produce H 2 in electrochemical CO 2 reduction reaction. To enhance the intrinsic catalytic activity, a metal-oxide heterogeneous interface was created via interfacial engineering modulation by loading Pd on CuO. The CuO/Pd electrode exhibited excellent electrochemical CO 2 reduction performance, with 54% Faraday efficiency at −0.65 V for CH 3 OH. [Display omitted] • The active site of the grass-like hydrophilic CuO electrode was verified to be oxide-derived Cu by the transition in wettability. • Pd loading on CuO by interfacial engineering both satisfies the reduction of CuO to Cu and also contributes to the increase of active sites. • The interfacial effect between CuO and Pd appreciably reduces the work function of CuO to promote CO 2 reduction. • The FE of CH 3 OH reach up to 54 % at −0.65 V over CuO/Pd-2. Copper-based catalysts have been extensively investigated in electrochemical carbon dioxide (CO 2) reduction to promote carbon products generated by requiring multiple electron transfer. However, hydrophilic electrodes are unfavourable for CO 2 mass transfer and preferentially hydrogen (H 2) evolution in electrochemical CO 2 reduction. In this paper, a hydrophilic cupric oxide (CuO) electrode with a grassy morphology was prepared. CuO-derived Cu was confirmed as the active site for electrochemical CO 2 reduction through wettability modulation. To enhance the intrinsic catalytic activity, a metal-oxide heterogeneous interface was created by engineering modulation at the interface, involving the loading of palladium (Pd) on CuO (CuO/Pd). Both the electrochemically active area and the electron transfer rate were enhanced by Pd loading, and significantly the reduced work function further facilitated the electron transfer between the electrode surface and the electrolyte. Consequently, the CuO/Pd electrode exhibited excellent excellent performance in electrochemical CO 2 reduction, achieving a 54 % Faraday efficiency at −0.65 V for methanol (CH 3 OH). The metal-oxide interfacial effect potentially improves the intrinsic catalytic activity of hydrophilic CuO electrodes in electrochemical CO 2 reduction, providing a conducive pathway for optimizing hydrophilic oxide electrodes in this process. [ABSTRACT FROM AUTHOR]

[Display omitted] • Co 2 N C with diatomic pair sites was successfully prepared. • Co 2 N C exhibited much faster degradation kinetic rate than Co 1 N C. • More ROS were generated by the catalysis of Co 2 N C. • DFT calculation further revealed the enhanced activity of Co 2 sites. A novel strategy for better catalytic performance in terms of precisely tuning the metal atom number of active centers is gradually getting attention. In this paper, the Co atom pair sites on N -doped porous carbon was engineered. The binuclear Co 2 site structure was identified by aberration-corrected scanning transmission electron microscopy and X-ray absorption spectroscopy. As expected, the Co 2 N C display an outstanding Fenton-like catalysis activity in tetracycline degradation with turnover frequency exceeding 0.91 min−1 that is approximately 4 times higher than the conventional CoN 4 site. The EPR tests indicated that the ROS strength stimulated by the binuclear site was much stronger than that of single site. Theoretical density functional theory calculations reveal that the optimized adsorption configuration is the O1 of peroxymonosulfate (PMS) interacting with two Co atoms, leading to stronger interaction effect and electron transfer for PMS comparing to single atom sites. [ABSTRACT FROM AUTHOR]

Small nuclear power plants are a promising direction of research for the development of carbon-free energy in isolated power systems and in remote regions with undeveloped infrastructure. Improving the efficiency of power units integrated with small modular reactors will improve the prospects for the commercialization of such projects. Power cycles based on supercritical carbon dioxide are an effective solution for nuclear power plants that use reactor facilities with an initial coolant temperature above 550 °C. However, the presence of low temperature rejected heat sources in closed Bryton cycles indicates a potential for energy saving. This paper presents a comprehensive thermodynamic analysis of the integration of an additional low-temperature organic Rankine cycle for heat recovery to supercritical carbon dioxide cycles. A scheme for sequential heat recovery from several sources in S-CO2 cycles is proposed. It was found that the use of R134a improved the power of the low-temperature circuit. It was revealed that in the S-CO2 Brayton cycle with a recuperator, the ORC add-on increased the net efficiency by an average of 2.98%, and in the recompression cycle by 1.7–2.2%. With sequential heat recovery in the recuperative cycle from the intercooling of the compressor and the main cooler, the increase in efficiency from the ORC superstructure will be 1.8%. [ABSTRACT FROM AUTHOR]

This paper addresses the problem of hydrogen generation from hydrocarbon gases using Steam Methane Reforming (SMR) with byproduct CO2 injected into and stored in a partially depleted oil reservoir. It focuses on the reservoir aspects of the problem using numerical simulation of the processes. To this aim, a numerical model of a real oil reservoir was constructed and calibrated based on its 30-year production history. An algorithm was developed to quantify the CO2 amount from the SMR process as well as from the produced fluids, and optionally, from external sources. Multiple simulation forecasts were performed for oil and gas production from the reservoir, hydrogen generation, and concomitant injection of the byproduct CO2 back to the same reservoir. EOR from miscible oil displacement was found to occur in the reservoir. Various scenarios of the forecasts confirmed the effectiveness of the adopted strategy for the same source of hydrocarbons and CO2 sink. Detailed simulation results are discussed, and both the advantages and drawbacks of the proposed approach for blue hydrogen generation are concluded. In particular, the question of reservoir fluid balance was emphasized, and its consequences were presented. The presented technology, using CO2 from hydrogen production and other sources to increase oil production, also has a significant impact on the protection of the natural environment via the elimination of CO2 emission to the atmosphere with concomitant production of H2. [ABSTRACT FROM AUTHOR]

Climate change, driven by anthropogenic activities, has far-reaching consequences for our planet. Among its many impacts, changes in temperature, elevated carbon dioxide levels, and shifts in greenhouse gas concentrations significantly affect soil ecosystems. In particular, soil microbial communities play a pivotal role in nutrient cycling, organic matter decomposition, and overall soil health. Soil microbial communities respond differently to the effects of climate change, like elevated warming and precipitation. The change in climatic conditions is reported to be adversely affecting soil biological activity directly through either drying or wetting of soil or affecting their associated plants. This review delves into the intricate relationship between climate change and soil microbial abundance, diversity, and distribution. The paper also discusses climatic change pressure on soil enzymatic activity and microbial biomasses, as well as soil faunal activity, as they are key indicators of soil health in a changing climate. Soil microbial communities cope with climate change by changing their diversity and physiological characteristics and by changing their symbiotic plants, which indicates the role of soil microbes in withstanding the negative impact of climate change. [ABSTRACT FROM AUTHOR]

Due to the nonlinear behavior of carbon dioxide properties at its critical point and the size effect of the supercritical carbon dioxide (S-CO2) centrifugal compressor, the stall causation mechanism differs between the S-CO2 centrifugal compressor and a conventional air compressor. The comprehension of the induced principle of the S-CO2 compressor rotating stall holds immense significance in enhancing stall margin and efficiency. This paper employs unsteady simulations to investigate the causes of the impeller rotating stall in the S-CO2 centrifugal compressor. The results show that the leading edge breakdown vortex (LEBV) formed by the tip leakage vortex (TLV) breakdown and the reverse flow in the passage are the reasons for blocking the passage and ultimately causing the rotating stall of the impeller. The migration motion of the LEBV not only induces the leading edge spillage phenomenon but also influences the intensity of the tip leakage flow (TLF) in adjacent passages, causing the propagation of the TLV breakdown phenomenon in the opposite direction to that of impeller rotation. The TLV undergoes intermittent breakdown in flow field, which is influenced by variations in TLF intensity. Additionally, there is a preceding process of breakdown-induced vortex formation and disappearance prior to TLV fragmentation. [ABSTRACT FROM AUTHOR]

Research has focused on the threat of global warming-induced climate change to modern human civilization. Carbon dioxide (CO2) is a primary greenhouse gas that causes global warming. Current efforts have focused on using CO2 as a raw source for producing value-added chemicals. Among the different CO2 conversion processes, the Sabatier process, also known as "CO2 methanation," is an effective approach, particularly if H2 is generated by renewable energy sources. In this process, methane (CH4) and water (H2O) are produced from CO2 and H2 using different transition-metal-based catalysts. Although numerous studies have been conducted to assess the significance of CO2 methanation, quantitative analysis of the publication trends in this research field is still lacking. This review presents the global research landscape of CO2 methanation over the last 20 years (2000–2022). The Web of Science (WoS) database was used to extract 1657 publications, and the VOSviewer software was used for bibliometric investigations. Bibliometric analysis revealed that 77.53% of the papers were published within the past 5 years (2018–2022). The International journal of hydrogen energy is leading journal publishing research articles about CO2 methanation followed by Applied Catalysis B. This study conducted a statistical analysis on the influence of leading countries, institutions, journals, authors, and top keywords in the field of CO2 methanation. Additionally, future research directions and findings of the most cited publications are discussed. Because the CO2 methanation reaction requires a highly stable and active catalyst, a brief introduction and major challenges of these catalysts are also reviewed. We hope that bibliometric findings will help scholars to understand this field of research more effectively and comprehensively. [ABSTRACT FROM AUTHOR]

Taking the Yangtze River Delta (YRD) of China as the research area, this paper studies the influence of freight structure adjustment and energy intensity on carbon dioxide (CO2) emission from the transportation industry. Sample data from 1990 to 2019 are selected, and co-integration analysis is performed using three independent variables: energy intensity, turnover ratio of railway to highway (R/H), and turnover ratio of railway to waterway (R/W). Then, an autoregressive distribution lag-error correction model (ARDL-ECM) is established to estimate the long-run and short-run relationships among the variables through unit root test, autoregressive distributed lag (ARDL) boundary test, and Granger test. The results show that in the long run, the growth of energy intensity leads to the long-term growth of CO2 emission in the transportation sector of the YRD, and R/W and R/H have a suppressive effect on CO2 emission. Granger causality indicates that there is a bidirectional causal relationship between energy intensity and CO2 emission. This work can be a reference for government departments to formulate policies related to carbon emissions in the transportation industry. [ABSTRACT FROM AUTHOR]

Energy generation and pollutant emissions are two faces of the same coin, as the current energy sources i.e., fossil energy, are still considered to be major sources of greenhouse gases (GHG). Therefore, shifting to cleaner energy sources imposes itself as an inevitable solution to reduce this environmental cost. In this paper, a hybrid system based on the multi-agent approach and Long Short-Term Memory (LSTM) neural networks to forecast the energy production and its carbon dioxide (CO2) emissions and simulate the potential emission reduction in case of switching to renewable energy sources is presented. The proposed system's architecture consists of combining LSTM models with the agent-based technology, where multiple LSTM forecasting models were trained to forecast the production of each type of the studied energies and then estimate the equivalent emitted CO2 and calculate the influence of the renewable energy inputs on the carbon emissions and the fossil fuels consumption. The simulation process consists of two phases: firstly, each forecasting agent uses a specific LSTM model to forecast short-term energy production. Secondly, these agents send the forecasted values to the coordination agent who is responsible for calculating the total CO2 emissions and the benefits of the renewable energy inputs. [ABSTRACT FROM AUTHOR]

As the atmospheric carbon dioxide (CO2) concentration rapidly rises, carbon capture, utilization, and storage (CCUS) is an emerging field for climate change mitigation. Various carbon capture technologies are in development with the help of adsorbents, membranes, solvent-based systems, etc. One of the main challenges in this field is the removal of CO2 from nitrogen (N2) gas. This paper focuses on mixed matrix membrane technology, for which the CO2/N2 separation performance is based on differences in gas permeations. Membrane separation and purification technologies are widely studied for carbon capture. Microporous adsorbents such as zeolites and metal organic frameworks (MOFs) for carbon capture have been attracting researchers' attention due to their highly porous structures, high selectivity values, and tunable porosities. Utilizing microporous adsorbents dispersed within a novel, blended polymer matrix, fourteen membranes were prepared with the commercial MOF ZIF-8, zeolite 13X, and kaolin, with methyl cellulose (MC) and polyvinyl alcohol (PVA), which were tested using a single gas permeation setup in this study. The addition of polyallylamine (PAH) as a chemisorbent was also investigated. These membranes were synthesized both with and without a polyacrylonitrile (PAN) support to compare their performances. MC was found to be an ideal polymeric matrix component to develop free-standing MMMs. At 24 °C and a relatively low feed pressure of 2.36 atm, a free-standing zeolite-13X-based membrane (MC/PAH/13X/PVA) exhibited the highest N2/CO2 selectivity of 2.8, with a very high N2 permeability of 6.9 × 107 Barrer. Upon the optimization of active layer thickness and filler weight percentages, this easily fabricated free-standing MMM made of readily available materials is a promising candidate for CO2 purification through nitrogen removal. [ABSTRACT FROM AUTHOR]

The paper reports the development of Cu-doped NiCo 2 O 4 ternary inverse spinel oxides through microwave-assisted hydrothermal method as effective catalysts for alkaline hydrogen evolution reaction (HER). The effective and controlled doping of Cu to NiCo 2 O 4 lattice by the partial replacement of Ni2+/Ni3+ with Cu+/Cu2+ results in the fine-tuning of structural, morphological, and electronic characteristics, favourable for electrocatalytic HER. The study effectively correlates the influence of variation in the percentages of Cu-doping on the material properties and thereby the electrocatalytic characteristics. The experimental results indicate that Cu 0.10 Ni 0.90 Co 2 O 4 electrode having optimum Cu-doping (10%) as the best electrocatalyst with the lowest onset potential for hydrogen evolution (242.7 mV) and reduced overpotential (72.5 mV) values by following a Volmer – Heyrovsky mechanism during HER. The improvement in HER performance after Cu-doping is due to the generation of greater number of active sites and reduction in electronic band gap. The present work advantageously utilises the scope of microwave-assisted transition metal doping strategy to fine tune the physicochemical and electronic characteristics, favourable for electrocatalytic HER, and this may pave a new way for tuning the electrochemical properties of metal oxides for various applications. • Microwave-assisted hydrothermal synthesis is used effectively to develop Cu-doped NiCo 2 O 4. • Cu-doping to NiCo 2 O 4 lattice creates more oxygen vacancies and improves electronic conductivity. • Cu 0.10 Ni 0.90 Co 2 O 4 with 10% Cu-doping exhibits promising electrocatalytic activity towards HER. • Cu-doped NiCo 2 O 4 follows Volmer – Heyrovsky mechanism during alkaline HER. [ABSTRACT FROM AUTHOR]

Carbon dioxide (CO2) capture and storage (CCS) is presented as an alternative measure and a promising approach to mitigate the large-scale anthropogenic CO2 emission into the atmosphere. In this context, CO2 sequestration into depleted oil and gas reservoirs is a practical approach as it boosts the recovery and facilitates the permanent storing of CO2 into the candidate sites. However, the estimation of CO2 storage capacity and properties in subsurface is a challenge to kick-start CCS worldwide. Thus, this paper characterizes the reservoirs of a field to tackle the challenge of CO2 emission and storage in Niger Delta. To achieve this work's ultimate goal, the Schulmberger Petrel software was used for evaluation of the structural and petrophysical parameters of six well logs, which includes faults for trapping mechanism, porosity and permeability. Eleven reservoir (A-K) storage units were delineated and reservoir A selected for CO2 storage within sand and shale lithologies. These storage units were furthermore subdivided into three: the shallow, middle and deeper reservoirs. The results demonstrated significant trapping structures, with good closure dependent fault pattern in a major NW-SE trending direction for CO2 storage without leakage. Also, the reservoir of study indicates 0.01 - 0.35 porosity and 0.5 -350MD permeability ranges respectively, which is a good indication of the ability of the reservoir rocks to retain and allow fluid to flow. Thus, reservoir A was chosen to possess the potential of CO2 storage and utilization due to well continuous sand geobody across the wells and its structural ability in Onshore Niger Delta. [ABSTRACT FROM AUTHOR]

This paper presents an experimental study of using a double-layered Cu/TiO2 and P4O10/TiO2 as photocatalysts for CO2 reduction with an extended wavelength of range light from ultraviolet light (UV) to infrared light (IR). The lights studied were UV + visible light (VIS) + IR, VIS + IR and IR only. This study also investigated the impact of the molar ratio of CO2:H2O on the CO2 reduction performance. This study revealed that the optimum molar ratio of CO2:H2O to produce CO was 1:1, irrespective of light illumination condition, which matched the theoretical molar ratio to produce CO according to the reaction scheme of CO2 reduction with H2O. Comparing the results of double-layered Cu/TiO2 and P4O10/TiO2 with those of double-layered TiO2 obtained under the UV + VIS + IR light illumination condition, the highest concentration of formed CO and the molar quantity of formed CO per unit weight of the photocatalyst increased by 281 ppmV and 0.8 μmol/g, in the case of the molar ratio of CO2:H2O = 1:1. With IR-only illumination, the highest concentration of formed CO and the molar quantity of CO formed per unit weight of the photocatalyst was 251 ppmV and 4.7 μmol/g, respectively. [ABSTRACT FROM AUTHOR]

Sweep efficiency of stagnant and poorly drained reservoir zones is extremely relevant task during gas and chemical flooding of hard-to-recover reserves. The paper presents the results of the field implementation of the in-situ CO2 generation technology to recovery of residual oil reserves and increase the sweep efficiency factor. The article presents the results of theoretical and laboratory studies, as well as field cases of an energy- and resource-saving method for oil recovery increase and improving oil production. The results of the reservoir stimulation confirmed the increase in the total incremental oil production after treatment operation on recovering residual oil reserves on. [ABSTRACT FROM AUTHOR]

The optimal discharge pressure is the essential factor affecting the operating performance of the transcritical CO 2 system. This paper presents a detailed study on the mechanism of the optimal discharge pressure from the perspective of fixed gas cooler outlet temperature and the heat transfer pinch point. The fixed gas cooler outlet temperature mainly analyzes the mechanism of the optimal discharge pressure from the enthalpy difference of isotherm in the supercritical region. The heat transfer pinch point mainly analyses the optimal discharge pressure at low inlet water temperatures, in which the subcritical region close to the critical point is considered. The effect of different parameters on optimal discharge pressure and system performance is discussed. The results indicate that the unique CO 2 physical properties and the pinch point in the gas cooler cause the optimal discharge pressure of the transcritical CO 2 system. The physical properties mainly affect the optimal discharge pressure at the high inlet water temperature, while the pinch point mainly affects the optimal discharge pressure at the low inlet water temperature. The inlet and outlet water temperatures are the most significant factors affecting the system's performance. [ABSTRACT FROM AUTHOR]

The supercritical CO2 power cycle driven by solar as a new generation of solar thermal power generation technology has drawn significant attention worldwide. In this paper, a cogeneration system derived from a supercritical CO2 recompression Brayton cycle is proposed, by considering the recovery of waste heat from the turbine outlet. The absorption refrigeration cycle is powered by the medium-temperature waste heat from the turbine outlet, while the low-temperature waste heat is employed for heating, achieving the cascaded utilization of the heat from the turbine outlet. As for the proposed combined cooling, heating, and power (CCHP) system, a dynamic model was built and verified in MATLAB R2021b/Simulink. Under design conditions, values for the energy utilization factor (EUF) and exergy efficiency of the cogeneration system were obtained. Moreover, the thermodynamic performances of the system were investigated in variable cooling/heating load and irradiation conditions. Compared with the reference system, it is indicated that the energy utilization factor (EUF) and exergy efficiency are 84.7% and 64.8%, which are improved by 11.5% and 10.3%. The proposed supercritical CO2 CCHP system offers an effective solution for the efficient utilization of solar energy. [ABSTRACT FROM AUTHOR]

Alternative solvents based on aqueous solutions of amino acids have been recently developed as possible substitutes for Mono Ethanol Amine (MEA) for CO2 removal from flue gas streams. The potassium taurate solvent has the advantages of degradation resistance, low toxicity and low energy requirements for its regeneration. With any type of solvent, CO2 removal applied to a power production plant decreases the revenues obtained from selling electricity because of the energy requirements. Operating the CO2 removal section in flexible mode avoids significant effects on the profits of the power plant, while accomplishing environmental regulations. This work is the first journal paper focusing on the application in flexible mode of the potassium taurate system for treating a flue gas stream from a 500 MW coal-fired power plant. Techno-economic evaluations are performed to determine the best operating conditions considering the variation in the electricity demand and its price, and different values of carbon tax. In the summer period, with high electricity prices and demands, carbon tax values between 45 EUR/tCO2 and 60 EUR/tCO2 favor CO2 absorption in the flexible mode, without periods of full CO2 emissions during the day. [ABSTRACT FROM AUTHOR]

The ability to efficiently separate CO2 from other light gases using membrane technology has received a great deal of attention due to its importance in applications such as improving the efficiency of natural gas and reducing greenhouse gas emissions. A wide range of materials has been employed for the fabrication of membranes. This paper highlights the work carried out to develop novel advanced membranes with improved separation performance. We integrated a polymerizable and amino acid ionic liquid (AAIL) with zeolite to fabricate mixed matrix membranes (MMMs). The MMMs were prepared with (vinylbenzyl)trimethylammonium chloride [VBTMA][Cl] and (vinylbenzyl)trimethylammonium glycine [VBTMA][Gly] as the polymeric support with 5 wt% zeolite particles, and varying concentrations of 1-butyl-3-methylimidazolium glycine, [BMIM][Gly] (5–20 wt%) blended together. The membranes were fabricated through photopolymerization. The extent of polymerization was confirmed using FTIR. FESEM confirmed the membranes formed are dense in structure. The thermal properties of the membranes were measured using TGA and DSC. CO2 and CH4 permeation was studied at room temperature and with a feed side pressure of 2 bar. [VBTMA][Gly]-based membranes recorded higher CO2 permeability and CO2/CH4 selectivity compared to [VBTMA][Cl]-based membranes due to the facilitated transport of CO2. The best performing membrane Gly-Gly-20 recorded permeance of 4.17 GPU and ideal selectivity of 5.49. [ABSTRACT FROM AUTHOR]