Search

This paper examines the impact of the CO2 laser parameters on the tensile strength, which is one of the most important properties of paper packaging in the process of cutting paper material. The study was performed on a paper material sample Fbb Board/Ningbo Spark C1S Ivory Board by examination of the influence of four independent variables: paper material grammage, cutting speed, laser power, and resolution on the tensile strength by using definitive screening design. Optimum process conditions of four variables that maximize the tensile strength were predicted and validated accordingly. Results confirm that laser power, paper material grammage, and cutting speed are the main process parameters that mostly affect the tensile strength. Besides individual parameters, two statistically significant interactions were obtained: laser power and cutting speed, and cutting speed and laser resolution. Maximum tensile strength values (20.37 N/mm) were achieved using the laser power of 60.6%, cutting speed of 3.24%, resolution of 2500 Hz, and a paper material grammage of 326.85 g/m2. With laser power at middle values and at a lower speed, a maximum tensile strength value can be obtained. Increasing the laser power and cutting speed will produce a slight lowering of tensile strength. [ABSTRACT FROM AUTHOR]

Flexible calcium carbonate (FCC) was developed as a functional papermaking filler for high loaded paper, which was a fiber-like shaped calcium carbonate produced from the in situ carbonation process on the cellulose micro-or nanofibril surface. Chitin is the second most abundant renewable material after cellulose. In this study, a chitin microfibril was utilized as the fibril core for making the FCC. Cellulose fibrils for the preparation of FCC were obtained by fibrillation of the TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl radical) treated wood fibers. The chitin fibril was obtained from the β-chitin from the born of squid fibrillated in water by grinding. Both fibrils were mixed with calcium oxide and underwent a carbonation process by the addition of carbon dioxide, thus the calcium carbonate attached on the fibrils to make FCC. When used in papermaking, both the FCC from chitin and cellulose gave a much higher bulk and tensile strength simultaneously than the conventional papermaking filler of ground calcium carbonate, while maintaining the other essential properties of paper. The FCC from chitin caused an even higher bulk and higher tensile strength than those of the FCC from cellulose in paper materials. Furthermore, the simple preparation method of the chitin FCC in comparison with the cellulose FCC may enable a reduction in the use of wood fibers, process energy, and the production cost of paper materials. [ABSTRACT FROM AUTHOR]

Lime mud, a kind of industrial waste that produced in paper mill, was proposed as CO2 sorbent in calcium looping process. The carbonation performance of the lime mud was investigated in a dual‐fixed bed reactor (DFR) and a thermogravimetric analyzer (TGA). The carbonation kinetics of the lime mud in the chemical reaction controlled stage was analyzed by a surface reaction‐controlled kinetic model. The results show that the lime mud presents much poorer carbonation performance during the chemical reaction controlled stage compared with the limestone, mainly due to the high content of chlorine in the lime mud. A prewash treatment process was used to decrease the chlorine content to mitigate the sintering of the lime mud when calcined at high temperature. After prewash treatment, the prewashed lime mud shows much higher CO2 capture capacity during the chemical reaction controlled stage compared with the lime mud. A prolonged carbonation process successfully further enhances the microstructure and improves the carbonation performance of the prewashed lime mud in the chemical reaction controlled stage. The lime mud can be effectively used as CO2 sorbent in calcium looping process after prewash treatment and the following prolonged carbonation treatment. [ABSTRACT FROM AUTHOR]

Utilization of the quality-upgraded waste paper in the manufacture of paper and board will reduce the wood consumption and pulping energy. While the optical property of the fibers from recycled old newspaper is very poor, in-situ calcium carbonate formation on those fibers by injecting carbon dioxide to the mixed slurry of those pulp and calcium oxide improved their brightness. Upgrading recycled old newspaper to substitute more expensive wood furnish, such as recycled old magazine, was successfully demonstrated in the present study. This study showed that the in-situ calcium carbonate formation process improved the optical quality of the recycled old newspaper by covering colored impurities with newly formed calcium carbonate, and improved calcium carbonate retention in papermaking process by attaching them to fibers. The strength reduction by the presence of newly formed calcium carbonate in the paper was recovered by adding strength agent. High ash retention at high ash content under the strong turbulence in the modern paper mill was achieved by the application of the in-situ calcium carbonate formation method. The quality-upgrade of recycled fibers and cost saving in the manufacture of duplex paperboard were demonstrated in the mill trial. [ABSTRACT FROM AUTHOR]

In 2017, a carbon emissions trading market will be launched nationwide by the China government. Calculating the enterprise carbon emissions is an important prerequisite and basis for trading. This paper discussed types of greenhouse gases, calculation boundaries and methods, energy consumption, carbon emissions, and intensity of a representative integrated pulp and paper mill in China based on China Guidance and Greenhouse Gas Protocol Tools. The results showed that there were 435,000 tonnes (t) of CO2 emissions from that mill in 2014 that did not contain emissions of biomass energy, which was 8 times higher than that of fossil energy. The pulp carbon intensity based on the mill was 0.230 t CO2/Adt, which accounted for 7.50% to 57.4% in other pulps' based on the product. Intensity based on Gross Domestic Product (GDP) was 1.090 t CO2e/1000 USD and accounted for 56.8% intensity in the China paper industry. The intensity based on sales accounted for 52.6% in the firstclass enterprise in the developed country. It also showed that intensity was influenced by the species of raw material, energy, and products, which provided the mill with measures for energy saving and emissions reduction to obtain the redundant carbon emissions in the trading. [ABSTRACT FROM AUTHOR]

Based on surface science, adsorption of mineral oil, water, gas products (typified by CO2 and CH4), and acids (typified by formic acid) on meta-aramid insulation paper has been investigated by molecular dynamics simulations. When the adsorption process finishes, the free volume fraction in the crystalline region is very small owing to the stable molecular arrangement of fiber. In addition, the number of pores on the surface of the meta-aramid fiber and the pore size are small, and the stable configuration of hydrogen bonds plays an important role, so it is difficult for the mineral oil and aging products to enter the meta-aramid crystalline region. The irregular arrangement of molecules in the amorphous region means that it is easier for the mineral oil and aging products to enter the amorphous region than the crystalline region, and the influence of these substances on the amorphous region is greater than that on the crystalline region. The order of the adsorption strengths of the four types of aging products on meta-aramid fiber is formic acid > water > CO2 > CH4. Therefore, it is necessary to monitor the acid and water contents in transformers with meta-aramid insulation paper as the solid insulation material. [ABSTRACT FROM AUTHOR]

Highlights • Synthetic CaO-based CO 2 sorbent was prepared using paper fibre as a biotemplate. • Synthetic sorbent is mainly composed of CaO and Ca 12 Al 14 O 33. • Synthetic sorbents possess microtube-like structure with superior CO 2 uptake. • Synthetic sorbent has improved sintering resistance in severe calcination condition. Abstract Calcium looping is regarded as an effective and viable way to address CO 2 emissions. To overcome the loss-in-capacity problems of calcium-based sorbents with the number of calcium looping cycles, a novel CaO/Ca 12 Al 14 O 33 sorbent with a microtube-like structure was prepared from carbide slag and Al(NO 3) 3 ·9H 2 O using paper fibre as a biotemplate. The CO 2 capture performance and microstructure of the novel synthetic sorbent under calcium looping conditions were investigated. The results show that the utilization of the biotemplate is good to retain the high cyclic CO 2 capture reactivity of the synthetic sorbent. Due to the unique hollow porous structure, the CO 2 capture capacity of the synthetic sorbent containing 7.5 wt% Al 2 O 3 retains 0.56 and 0.33 g/g after 30 cycles under mild and severe calcination conditions, respectively, which are 2.56 and 2.11 times higher than those of carbide slag under the same respective calcination conditions. With the presence of 10% steam in the carbonation atmosphere, the CO 2 capture capacity of the synthetic sorbent retains 0.55 g/g under the severe calcination conditions after 10 cycles. The native hierarchical biostructure of paper fibre is preserved in the synthetic sorbent. CaO and Ca 12 Al 14 O 33 are uniformly distributed in the synthetic sorbent, resulting in a high sintering resistance during multiple CO 2 capture cycles. CO 2 can penetrate through the microtube-like structure of the synthetic sorbent from two directions, i.e., from the outer surface and inner surface. This phenomenon effectively enlarges the contact area between CO 2 and CaO. The CaO/Ca 12 Al 14 O 33 sorbent with a hollow porous structure by means of a biotemplate appears promising in the calcium looping technology for CO 2 capture. [ABSTRACT FROM AUTHOR]

History has been kind to Christian Bohr (1855-1911). His name is attached eponymously to three different areas of respiratory physiology. The first is the Bohr dead space, which refers to the portion of the tidal volume that does not undergo gas exchange. The second is the increase in oxygen affinity of hemoglobin caused by the addition of carbon dioxide to the blood. This is known as the Bohr effect and is a very important feature of gas exchange, both in the lung and in peripheral tissues. Both of these contributions by Bohr are familiar to most students. Bohr's third contribution refers to the calculation of the changes in the PO2 of blood as oxygen is loaded in the pulmonary capillary, the so-called Bohr integration. This contribution is less well known now, partly because of the advent of digital computing, but it was important in its day. The analysis is challenging because the very nonlinear shape of the oxygen dissociation curve means that the PO2 difference between the alveolar gas and the capillary blood, which is the driving pressure for diffusion, changes in a complicated way. All three papers are in German, and two of them are long and tedious to read. English translations are available, but few people read the papers, despite the fact that the first two articles are very frequently cited. In the present article, Bohr's contributions are reviewed, and some parts of the articles that are particularly difficult to understand are clarified. [ABSTRACT FROM AUTHOR]

Key long-lived greenhouse gases (CO2, CH4, and N2O) are perhaps among the best-studied components of the Earth's atmosphere today; however, attempts to predict or explain trends or even shorter-term variations of these trace gases are not always successful. Infrared spectroscopy is a recognized technique for the ground-based long-term monitoring of the gaseous composition of the atmosphere. The current paper is focused on the analysis of new data on CO2, CH4, and N2O total columns (TCs) retrieved from high resolution IR solar spectra acquired during 2009–2022 at the NDACC atmospheric monitoring station of St. Petersburg State University (STP station, 59.88°N, 29.83°E, 20 m asl.). The paper provides information on the FTIR system (Fourier-transform infrared) installed at the STP station, and an overview of techniques used for the CO2, CH4, and N2O retrievals. Trends of key greenhouse gases and their confidence levels were evaluated using an original approach which combines the Lomb–Scargle method with the cross-validation and bootstrapping techniques. As a result, the following fourteen-year (2009–2022) trends of TCs have been revealed: (0.56 ± 0.01) % yr−1 for CO2; (0.46 ± 0.02) % yr−1 for CH4; (0.28 ± 0.01) % yr−1 for N2O. A comparison with trends based on the EMAC numerical modeling data was carried out. The trends of greenhouse gases observed at the STP site are consistent with the results of the in situ monitoring performed at the same geographical location, and with the independent estimates of the global volume mixing ratio growth rates obtained by the GAW network and the NOAA Global Monitoring Laboratory. There is reasonable agreement between the CH4 and N2O TC trends for 2009–2019, which have been derived from FTIR measurements at three locations: the STP site, Izaña Observatory and the University of Toronto Atmospheric Observatory. [ABSTRACT FROM AUTHOR]

Activated carbon fiber paper (ACFP) has the potential for adsorption due to their high surface area and low through resistance. In this work, free-standing ACFP was developed from fibrillated polyacrylonitrile (PAN) fiber through wet forming process combined with subsequent pre-oxidation, carbonization and CO 2 activation. A PFI refiner was used to prepare fibrillated PAN fibers with a beating degree of 7, 11, 25 and 60 oSR, respectively. As expected, PAN fibers with high beating degree improved surface area and fine fiber content, which resulted in the dense structure and low porosity of paper, thus influencing later stabilization and pyrolysis, as well as final properties of ACFP. With the increase of beating degree, the oxygen content of pre-oxidized PAN paper increased, but the cyclization index first decreased and then increased. ACFP with higher beating degree possessed higher BET surface area, pore volume and CO 2 uptake capacity. ACFP, prepared from freeze-dried PAN paper, performed better in physicochemical properties than that from plate-press drier under the same beating degree. This study exhibited that ACFP can be a special material featured by scale production, lightweight, and high microporosity of chemical adsorption and separation. [Display omitted] • ACFPs were prepared from fibrillated PAN fiber through wet forming process. • Effects of pore structure of PAN papers on physicochemical properties of ACFPs • CO 2 adsorption on ACFPs was a combined effects of physisorption and chemisorption. [ABSTRACT FROM AUTHOR]

This article presents an algorithm for modelling an Adaptive Neuro Fuzzy Inference System (ANFIS) for power transformer paper conditions in order to estimate the transformer's expected life. The dielectric characteristics, dissolved gasses, and furfural of 108 running transformers were collected, which were divided into 76 training datasets and another 32 testing datasets. The degree of polymerization (DP) of the transformer paper was predicted using the ANFIS model based on using the dielectric characteristics and dissolved gases as input. These inputs were analyzed, and the best combination was selected, whereas CO + CO2, acidity, interfacial tension, and color were correlated with the paper's deterioration condition and were chosen as the input variables. The best combination of input variables and membership function was selected to build the optimal ANFIS model, which was then compared and evaluated. The proposed ANFIS model has 89.07% training accuracy and 85.75% testing accuracy and was applied to a transformer paper insulation assessment and an estimation of the expected life of four Indonesian transformers for which furfural data is unavailable. This proposed algorithm can be used as a furfural alternative for the general assessment of transformer paper conditions and the estimation of expected life and provides a helpful assistance for experts in transformer condition assessment. [ABSTRACT FROM AUTHOR]

The pulp and paper (P&P) sector is a dynamic manufacturing industry and plays an essential role in the Austrian economy. However, the sector, which consumes about 20 TWh of final energy, is responsible for 7% of Austria's industrial CO2 emissions. This study, intending to assess the potential for improving energy efficiency and reducing emissions in the Austrian context in the P&P sector, uses a bottom-up approach model. The model is applied to analyze the energy consumption (heat and electricity) and CO2 emissions in the main processes, related to the P&P production from virgin or recycled fibers. Afterward, technological options to reduce energy consumption and fossil CO2 emissions for P&P production are investigated, and various low-carbon technologies are applied to the model. For each of the selected technologies, the potential of emission reduction and energy savings up to 2050 is estimated. Finally, a series of low-carbon technology-based scenarios are developed and evaluated. These scenarios' content is based on the improvement potential associated with the various processes of different paper grades. The results reveal that the investigated technologies applied in the production process (chemical pulping and paper drying) have a minor impact on CO2 emission reduction (maximum 10% due to applying an impulse dryer). In contrast, steam supply electrification, by replacing fossil fuel boilers with direct heat supply (such as commercial electric boilers or heat pumps), enables reducing emissions by up to 75%. This means that the goal of 100% CO2 emission reduction by 2050 cannot be reached with one method alone. Consequently, a combination of technologies, particularly with the electrification of the steam supply, along with the use of carbon-free electricity generated by renewable energy, appears to be essential. [ABSTRACT FROM AUTHOR]

As the second most predominant greenhouse gas, methane-targeted emission mitigation holds the potential to decelerate the pace of global warming. Satellite remote sensing is an important monitoring tool, and we review developments in the satellite detection of methane. This paper provides an overview of the various types of satellites, including the various instrument parameters, and describes the different types of satellite retrieval algorithms. In addition, the currently popular methane point source quantification method is presented. Based on existing research, we delineate the classification of methane remote sensing satellites into two overarching categories: area flux mappers and point source imagers. Area flux mappers primarily concentrate on the assessment of global or large-scale methane concentrations, with a further subclassification into active remote sensing satellites (e.g., MERLIN) and passive remote sensing satellites (e.g., TROPOMI, GOSAT), contingent upon the remote sensing methodology employed. Such satellites are mainly based on physical models and the carbon dioxide proxy method for the retrieval of methane. Point source imagers, in contrast, can detect methane point source plumes using their ultra-high spatial resolution. Subcategories within this classification include multispectral imagers (e.g., Sentinel-2, Landsat-8) and hyperspectral imagers (e.g., PRISMA, GF-5), contingent upon their spectral resolution disparities. Area flux mappers are mostly distinguished by their use of physical algorithms, while point source imagers are dominated by data-driven methods. Furthermore, methane plume emissions can be accurately quantified through the utilization of an integrated mass enhancement model. Finally, a prediction of the future trajectory of methane remote sensing satellites is presented, in consideration of the current landscape. This paper aims to provide basic theoretical support for subsequent scientific research. [ABSTRACT FROM AUTHOR]

ZnZrOx has been used in large quantities for the preparation of light olefins from CO2, but the relationship between structure and performance remains unclear at present. In this paper, ZnZrOx were prepared by co-precipitation method, and a series of oxides with different sizes were prepared by varying the calcination temperatures. Subsequently, these oxides were combined with SAPO-34 to create a composite bifunctional catalyst for the synthesis of light olefins by CO2 hydrogenation, in which the impact of nanocrystal size effect was examined. The catalytic performance significantly increased as the nanocrystal size reduced from 18 to 12 nm. However, when the nanocrystal size was further decreased to 8 nm, the catalytic performance decline. Characterizations revealed a gradual increase in the number of oxygen vacancies with decreasing nanocrystal size. However, the oxide with the smallest nanocrystal size, prepared by varied calcination temperatures, did not yield the optimal catalytic performance due to sintering occurring during the reaction process. The results show that the assumption that smaller nanocrystal sizes inherently equate to improved catalytic performance is not universally valid, and stability must be considered when the nanocrystal size is decreased. The bifunctional catalysts used in this paper for the prepared light olefins from CO2 in yield as high as 13.8%, which is higher than most previous reports. [ABSTRACT FROM AUTHOR]

Christian environmental ethics have always navigated the thin line between the Scylla of pantheism and the Charybdis of deism. On the one hand, removing God from the world avoids pantheism but can inadvertently render the divine a distant, absentee father who cares little about what we do with the environment. On the other hand, if we bring the Creator too close to creation, we may begin to blur the distinction between them, fringing on pantheism. While making nature divine might at first seem to heighten the environmental desecration of the earth by making it a literal de-sacralizing of the sacred, this may be only a surface-level reading (or, at least, only true of very carefully nuanced versions of pantheism). For the pantheist, God would not just be the trees but the machines that log them; God would not just be the polar bears but the carbon dioxide that is evicting them. God would be no more present in that which is desecrated than in that which does the desecration (e.g., God would be one with the pesticides, bulldozers, and factory smoke). By making God everything, it becomes difficult to call any person, act, legislation, or event godless. This paper offers Henry More's view of divine space as a constructive, Platonic Christian middle way between these two extremes, charting a God who is spatially present to nature without being pantheistically reducible to it, in the same way that space is intimately close to the objects within it while nonetheless remaining distinct from them. The bulk of the paper counters potential opponents to this proposal, specifically defending Morean space from the charge that it would break down the Creator–creature distinction and/or cave to the environmental Scylla of pantheism. [ABSTRACT FROM AUTHOR]

• Freestanding carbon paper confined with ultrafine lithiophilic TiO 2 is in-situ synthesized from MXene and CO 2. • Freestanding C/TiO 2 paper is firstly employed as dendrite-free Li metal anodic host. • The growth behaviors of metallic Li on C/TiO 2 is systematically probed. • Lithiophilic TiO 2 seeds and conductive 3D carbon synergistically induce dendrite-free Li deposition. • C/TiO 2 @Li paper enables full cell with improved electrochemical performance. Lithium (Li) metal anode is deemed as one of the most fascinating anodes due to its high energy density. Nonetheless, low Coulombic efficiency and safety issues caused by detrimental Li dendrites growth severely hamper its practical application. Herein, we construct an ultrafine TiO 2 confined in 3D freestanding carbon paper by one-step green in-situ oxidation of Ti 3 C 2 T x MXene film with greenhouse gas CO 2. The lithiophilic TiO 2 seeds and freestanding 3D carbon matrix can synergistically induce uniform Li deposition and buffer the volume changes during lithium striping and deposition, which ensure improved electrochemical performance with high Coulombic efficiency and low overpotential, etc. The growth process of metallic Li on C/TiO 2 is also systematically investigated. Moreover, the C/TiO 2 @Li||LiFePO 4 full batteries present a stable cycling performance over 250cycles at 1.0C and superior rate performance. Additionally, this work proposes an alternative way to utilize CO 2 , which may alleviate greenhouse effect and boost sustainable development. These results may be useful for both the design of dendrite-free lithium metal batteries and the sustainable utilizing of CO 2. [ABSTRACT FROM AUTHOR]

Pulp and paper is considered to be the fourth most energy-intensive industry (EII) worldwide. However, as most of the CO 2 emissions are of biomass origin, this sector has the potential to become a carbon-negative industry. This study proposes a new concept for conversion of the pulp and paper industry to carbon negative that relies on the inherent CO 2 capture capability of the Kraft process. The techno-economic performance of the proposed carbon-negative system, based on calcium looping (CaL) retrofitted to a pulp and paper plant, was evaluated. The effect of CaL design specifications and cost assumptions on the thermodynamic and economic performance were evaluated. Under the initial design assumptions, the reference pulp and paper plant was shown to turn from electricity importer to electricity exporter with the cost of CO 2 avoided equal to 39.0 €/tCO 2. The parametric study showed that an increase in the fresh limestone make-up rate resulted in a linear increase of the specific primary energy consumption for CO 2 avoided (SPECCA) and a reduction in the amount of electricity exported to the electric grid. This translates into an increase in the price of pulp and newsprint, and the cost of CO 2 avoided. This study has also demonstrated that the pulp and paper industry has high potential to become carbon negative. It has been shown that carbon capture and storage would become economically viable in this industry if the negative CO 2 emissions are recognised and a negative CO 2 emissions credit of at least 41.8 €/tCO 2 is implemented. • Concept of the Kraft process with inherent CO 2 capture. • Calcium looping for CO 2 capture is integrated in the lime cycle. • Reference pulp and paper plant turns from importer to exporter of electricity. • Pulp and paper industry has a high potential to become carbon negative. • Economic feasibility needs the inclusion of biogenic emissions in emission trading. [ABSTRACT FROM AUTHOR]

In order to improve the whiteness of fly ash, the particles were coated by in-situ precipitation of calcium carbonate. After different mass ratios of calcium oxide to fly ash were mixed into water, a certain amount of carbon dioxide was bubbled into the mixture to form a precipitated calcium carbonate deposit on the surface of fly ash. With the help of scanning electron microscopy (SEM), the process and the coating mechanism of the unmodified and modified fly ash were studied. The results showed that when a 1:1 mass ratio of calcium oxide to fly ash was implemented, the whiteness of fly ash was increased from 30.3 (the original fly ash) to 74.0 (the modified fly ash). After appropriately controlling for the rate of carbon dioxide, the whiteness was improved to meet the standard for filler in the papermaking industry, and also great advantages in paper physical strength were demonstrated. [ABSTRACT FROM AUTHOR]

This paper presents and analyzes a finite volume scheme for a fully degenerate parabolic system modeling the compressible two-phase flow, such as water-gas, problem in porous media considering the effects of temperature. The problem is written in terms of the phase formulation, i.e. the saturation of one phase, the pressure of the second phase and the temperature are primary unknowns. We use a first-order time implicit Euler scheme. The spatial discretization uses a fully coupled fully implicit cell-centered two-point flux approximation scheme where upwinding of the flux across an interface between two control volumes is performed for each fluid phase. Under physically relevant assumptions on the data, we prove the maximum principle for both saturation and temperature. We obtain a priori estimates and we show that the discrete problem is well posed. Also, we exploit various a priori estimates as well as compactness arguments to establish the convergence of the numerical scheme toward the weak solution. The open-source platform DuMu X was employed for the implementation of the developed algorithm based on the above scheme. Numerical result are presented to demonstrate the efficiency of this scheme. The test addresses the evolution in 2D of CO 2 injection into a layered aquifer. The algorithm's convergence with first order is validated by our numerical results, which support the theoretical results. To our best knowledge, this is the first convergence result of a finite volume scheme in the case of nonisothermal immiscible compressible two-phase flow in porous media. [ABSTRACT FROM AUTHOR]

Increased warming in the Arctic is of great concern. This is particularly due to permafrost degradation, which is expected to accelerate microbial breakdown of soil organic carbon, with its further release into the atmosphere as carbon dioxide (CO2). The fine-scale variability of CO2 fluxes across highly mosaic Arctic tundra landscapes can provide us with insights into the diverse responses of individual plant communities to environmental change. In the paper, we contribute to filling existing gaps by investigating the variability of CO2 flux rates within different landscape units for dominant vegetation communities and plant species across typical tundra of the southern part of the Taimyr Peninsula, Siberia. In general, the variability of soil CO2 flux illustrates a four-fold increase from non-vascular vegetation, mainly lichens and mosses (1.05 ± 0.36 µmol m−2 s−1), towards vascular plants (3.59 ± 0.51 µmol m−2 s−1). Barren ground ("frost boils") shows the lowest value of 0.79 ± 0.21 µmol m−2 s−1, while considering the Arctic "browning" phenomenon, a further substantial increase of CO2 flux can be expected with shrub expansion. Given the high correlation with top soil temperature, well-drained and relatively dry habitats such as barren ground and non-vascular vegetation are expected to be the most sensitive to the observed and projected temperature growth in the Arctic. For mixed vegetation and vascular species that favor wetter conditions, soil moisture appears to play a greater role. Based on the modeled seasonal pattern of soil CO2 flux and precipitation records, and applying the rainfall simulations in situ we outlined the role of precipitation across enhanced CO2 emissions (i.e., the "Birch" effect). We found that a pulse-like growth of soil CO2 fluxes, observed within the first few minutes after rainfall on vegetated plots, reaches 0.99 ± 0.48 µmol m−2 s−1 per each 1 mm of precipitation, while barren ground shows 55–70% inhibition of CO2 emission during the first several hours. An average additive effect of precipitation on soil CO2 flux may achieve 7–12% over the entire growing season, while the projected increased precipitation regime in the Arctic may strengthen the total CO2 release from the soil surface to the atmosphere during the growing season. [ABSTRACT FROM AUTHOR]

Under-deposit corrosion is widely present in the pipelines of oil and gas production, causing significant corrosion damage. In this paper, a novel electrochemical cathodic-polarization method was carried out to accelerate the formation of CaCO3 scale on a X65 steel surface in a simulated solution containing scaling ions. Subsequently, pre-scaled X65 steel was placed in a high temperature and pressure autoclave to conduct corrosion weight-loss experiments and in situ electrochemical measurements. The study mainly compared the corrosion inhibition behavior of four quaternary ammonium salt corrosion inhibitors, pyridinium quaternary salt (BPC), quinolinium quaternary salt (BQC), 8-hydroxyquinolinium quaternary salt (BHQ) and pyridinium (1-chloromethyl naphthalene) quaternary salt (1-CPN), in a simulated oilfield scale under corrosive conditions. The results of the weight-loss experiments demonstrated that the inhibition efficiencies of the corrosion inhibitors from high to low were as follows: 1-CPN < BHQ < BQC < BPC. The in situ electrochemical measurements showed that the immersion time and type of corrosion inhibitor had a pronounced influence on the corrosion and corrosion inhibition behavior of X65 steel with CaCO3 coating. It was also proved using both EIS and PC that 1-CPN shows the best inhibition performance in all. Lastly, the inhibition mechanism of corrosion inhibitors at under-deposit conditions was analyzed via a surface morphology observation of SEM. [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]

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]

The extensive utilization of fossil fuels has led to a rapid increase in atmospheric CO2 concentration, resulting in various environmental issues. To reduce reliance on fossil fuels and mitigate CO2 emissions, it is important to explore alternative methods of utilizing CO2 and H2 as raw materials to obtain high-value-added chemicals or fuels. One such method is CO2 methanation, which converts CO2 and H2 into methane (CH4), a valuable fuel and raw material for other chemicals. However, CO2 methanation faces challenges in terms of kinetics and thermodynamics. The reaction rate, CO2 conversion, and CH4 yield need to be improved to make the process more efficient. To overcome these challenges, the development of suitable catalysts is essential. Non-noble metal catalysts have gained significant attention due to their high catalytic activity and relatively low cost. In this paper, the thermodynamics and kinetics of the CO2 methanation reaction are discussed. The focus is primarily on reviewing Ni-based, Co-based, and other commonly used catalysts such as Fe-based. The effects of catalyst supports, preparation methods, and promoters on the catalytic performance of the methanation reaction are highlighted. Additionally, the paper summarizes the impact of reaction conditions such as temperature, pressure, space velocity, and H2/CO2 ratio on the catalyst performance. The mechanism of CO2 methanation is also summarized to provide a comprehensive understanding of the process. The objective of this paper is to deepen the understanding of non-noble metal catalysts in CO2 methanation reactions and provide insights for improving catalyst performance. By addressing the limitations of CO2 methanation and exploring the factors influencing catalyst effectiveness, researchers can develop more efficient and cost-effective catalysts for this reaction. [ABSTRACT FROM AUTHOR]

The accumulation of carbon dioxide in the atmosphere due to fossil fuel burning and deforestation has caused global warming and an increase in extreme weather events. To complement the shift towards clean energy, it is crucial to adopt methods for carbon dioxide removal, known as negative emission technologies. Enhanced weathering is one such approach that involves accelerating the natural process of rock weathering by spreading finely ground rocks over large areas, such as agricultural land or coastal areas. This exploratory review paper provides an overview of the fundamental mechanisms behind enhanced weathering, and outlines the techniques for its implementation. The environmental benefits of enhanced weathering are highlighted, including carbon dioxide removal, and improvement of soil fertility. Furthermore, potential impacts on ecosystems and biodiversity are examined, along with the effects on water, soil and air quality. The paper also considers the risks and challenges associated with large-scale implementation and long-term stability of enhanced weathering. Additionally, the integration of enhanced weathering with Sustainable Development Goals is explored, along with the potential co-benefits and trade-offs with other sustainability objectives. To conclude, this exploratory review paper summarizes the key findings and proposes avenues for further research in this field of enhanced weathering. [ABSTRACT FROM AUTHOR]

Near-surface oceanic turbulence plays an important role in the exchange of mass, momentum, and energy between the atmosphere and the ocean. The climate modifying the air–sea CO 2 transfer rate varies linearly with the surface turbulent kinetic energy dissipation rate to the 1 / 4 power in a range of systems with different types of forcing, such as coastal oceans, river estuaries, large tidal freshwater rivers, and oceans. In the first part of this paper, we present a numerical study of the near-surface turbulent kinetic energy spectra deduced from a direct numerical simulation (DNS) compared to turbulent kinetic energy spectra deduced from idealized infrared (IR) images. The DNS temperature fields served as a surrogate for IR images from which we have calculated the underlying kinetic energy spectra. Despite the near-surface flow region being highly anisotropic, we demonstrated that modeled isotropic and homogeneous turbulence spectra can serve as an approximation to observed near-surface spectra within the inertial and dissipation ranges. The second part of this paper validates our numerical observations in a laboratory experiment. In this experiment, we compared the turbulent kinetic energy spectra near the surface, as measured using a submerged shear sensor with the spectra derived from infrared images collected from above the surface. The energy dissipation measured by the shear sensor was found to be within 20% of the dissipation value derived from the IR images. Numerically and experimentally, we have demonstrated that IR-based and remote measurement techniques of the aquatic near surface offer a potentially accurate and non-invasive way to measure near-surface turbulence, which is needed by the community to improve models of oceanic air–sea heat, momentum, and gas fluxes. [ABSTRACT FROM AUTHOR]

Amid the global emphasis on efficient power conversion systems under the "dual carbon" policy framework, the supercritical CO2 (SCO2) Brayton cycle is a noteworthy subject, owing to its pronounced efficiency, compact design, economic viability, and remarkable potential to increase the thermal cycle efficiency of nuclear reactors. However, its application across various nuclear reactor loops presents divergent challenges, complicating system design and analytical processes. This paper offers a thorough insight into the latest research on the SCO2 Brayton cycle, particularly emphasising its integration within directly and indirectly cooled nuclear reactors. The evolution of the Brayton cycle in nuclear reactor systems has been meticulously explored, focusing on its structural dynamics, key components, and inherent pros and cons associated with distinct reactor loops. Based on the theoretical frameworks and empirical findings related to turbomachinery and heat exchangers within the cycle, we chart a course for future enquiries into its critical components, underscoring the indispensable role of experimental investigations. This paper conclusively assesses the feasibility of deploying the SCO2 Brayton cycle in direct and indirect cooling contexts, offering a forward-looking perspective on its developmental trajectory. The SCO2 Brayton cycle may become a focal point for research, potentially creating avenues for nuclear energy endeavours. [ABSTRACT FROM AUTHOR]

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]

We report herein the preparation and characterization of six readily assembled bis-coordinated homoleptic silver(I) N,N′-bis(arylimino)acenaphthene (BIAN) complexes of general structure [Ag(I)(BIAN)2]BF4 and the influence of the electronic properties of the ligand substitution pattern on their performance in electrochemical CO2 reduction (CO2R). All the explored catalysts displayed substantial current enhancements in carbon-dioxide-saturated solvents dependent on the ligated BIAN and no significant concurrent H2 evolution when utilizing 2% H2O as a proton source. Additionally, preliminary studies, employing a drop-casted ink of 0.4 mg cm−2 [Ag(I)(4-OMe-BIAN)2]BF4 (Ag4) immobilized onto carbon paper gas diffusion electrodes in a flow cell with 1M KHCO3 aqueous electrolyte, resulted in a propitious Faradaic efficiency of 51% for CO at a current density of 50 mA cm−2. [ABSTRACT FROM AUTHOR]

[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]

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]

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]

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]

The storage potential of hydrocarbon reservoirs in the central Gulf of Mexico (GOM) makes future development of CO2 storage projects in those areas promising for secure, large-scale, and long-term storage purposes. Focusing on the producing and depleted hydrocarbon fields in the continental slope of the central GOM, this paper analyzed, assessed, and screened the producing sands and evaluated their CO2 storage potential. A live interactive CO2 storage site screening system was built in the SAS® Viya system with a broad range of screening criteria combined from published studies. This offers the users a real-time assessment of the storage sites and enables them to adjust the filters and visualize the results to determine the most suitable filter range. The CO2 storage resources of the sands were estimated using a volumetric equation and the correlation developed by the National Energy Technology Laboratory (NETL). The results of this study indicate that 1.05 gigatons of CO2 storage resources are available in the developed reservoirs at the upper slope area of the central GOM. The Mississippi Canyon and Green Canyon protraction areas contain the fields with the largest storage resources. [ABSTRACT FROM AUTHOR]

Due to its cost-effectiveness and high product selectivity, tin oxide has been regarded as a promising catalyst for the electrochemical conversion of CO2 to formate. However, formate production is hindered by the high overpotential; there is a need to reduce the overpotential to enhance energy efficiency and lower electricity cost for the implementation of carbon utilization technology. Here, we report a facile synthesis method for 1 nm-sized SnO2 cluster catalysts, which can be used for CO2-to-formate conversion. SnO2 clusters were prepared through impregnation of porous carbon with a tin precursor solution. The SnO2 clusters showed a low overpotential, generating a current density of 10 mA cm-2 at a potential of -0.34 V vs. RHE in 1 M KOH. They also achieved high Faradaic efficiencies of 90.5% and 81.5% at 200 and 300 mA cm−2, respectively. Their electrocatalytic performance was strongly dependent on the annealing conditions, which affected the particle size, electrochemical active surface area, and metal oxidation state. This paper presents a versatile method for synthesizing metal oxide cluster catalysts, apart from providing insights into the catalytic activity for the electrochemical conversion of CO2 to formate. [ABSTRACT FROM AUTHOR]

Climatologies, which depict mean fields of oceanographic variables on a regular geographic grid, and atlases, which provide graphical depictions of specific areas, play pivotal roles in comprehending the societal vulnerabilities linked to ocean acidification (OA). This significance is particularly pronounced in coastal regions where most economic activities related to commercial and recreational fisheries as well as aquaculture industries occur. In this paper, we unveil a comprehensive data product featuring coastal climatologies and atlases for ten OA indicators, including fugacity of carbon dioxide, pH on the total scale, total hydrogen ion content, free hydrogen ion content, carbonate ion content, aragonite saturation state, calcite saturation state, Revelle Factor, total dissolved inorganic carbon content, and total alkalinity content. These indicators are provided on 1°×1° degree spatial grids at 14 standardized depth levels, ranging from the surface to a depth of 500 meters, along the North American ocean margins – defined as the region between the coastline and a distance of 200 nautical miles (∼370 km) offshore. The climatologies and atlases were developed using the World Ocean Atlas (WOA) gridding methods of the NOAA National Centers for Environmental Information (NCEI), based on the recently released Coastal Ocean Data Analysis Product in North America (CODAP-NA), along with the 2021 update to the Global Ocean Data Analysis Project version 2 (GLODAPv2.2021) data product. The relevant variables were adjusted to the index year of 2010. The data product is available in NetCDF (DOI: 10.25921/g8pb-zy76) at the NOAA Ocean Carbon and Acidification Data System: https://www.ncei.noaa.gov/data/oceans/ncei/ocads/metadata/0270962.html. It is recommended to use the objectively analyzed mean fields (with '_an' suffix) for each variable. The atlases can be accessed at: https://www.ncei.noaa.gov/access/ocean-carbon-acidification-data-system/synthesis/nacoastal.html. [ABSTRACT FROM AUTHOR]

The paper presents the results of experimental and model studies of the pressure swing adsorption (PSA) process in a column with a zeolite 13X bed with a height of 0.5 m. The gas mixture consisted of CO2 (10–20%), N2, and H2O (RH 50%) in different ratios. As a result of the column tests, concentration, and temperature evolutions were obtained for each of the adsorption and desorption stages, which were used to determine the breakthrough and bed saturation times and other parameters important for the analysis of the column operation. A mathematical model of the PSA process for the separation of CO2 from the gas mixture was developed. The system of second-order partial differential equations was solved using Matlab software. The research focuses on adsorptive CO2 capture and shows the influence of water vapor and operational parameters on the quality of model validation. [ABSTRACT FROM AUTHOR]

The quantification of emissions of greenhouse gases and air pollutants through the inversion of plumes in satellite images remains a complex problem that current methods can only assess with significant uncertainties. The anticipated launch of the CO2M (Copernicus Anthropogenic Carbon Dioxide Monitoring) satellite constellation in 2026 is expected to provide high-resolution images of CO2 (carbon dioxide) column-averaged mole fractions (XCO2), opening up new possibilities. However, the inversion of future CO2 plumes from CO2M will encounter various obstacles. A challenge is the low CO2 plume signal-to-noise ratio due to the variability in the background and instrumental errors in satellite measurements. Moreover, uncertainties in the transport and dispersion processes further complicate the inversion task. To address these challenges, deep learning techniques, such as neural networks, offer promising solutions for retrieving emissions from plumes in XCO2 images. Deep learning models can be trained to identify emissions from plume dynamics simulated using a transport model. It then becomes possible to extract relevant information from new plumes and predict their emissions. In this paper, we develop a strategy employing convolutional neural networks (CNNs) to estimate the emission fluxes from a plume in a pseudo- XCO2 image. Our dataset used to train and test such methods includes pseudo-images based on simulations of hourly XCO2 , NO2 (nitrogen dioxide), and wind fields near various power plants in eastern Germany, tracing plumes from anthropogenic and biogenic sources. CNN models are trained to predict emissions from three power plants that exhibit diverse characteristics. The power plants used to assess the deep learning model's performance are not used to train the model. We find that the CNN model outperforms state-of-the-art plume inversion approaches, achieving highly accurate results with an absolute error about half of that of the cross-sectional flux method and an absolute relative error of ∼ 20 % when only the XCO2 and wind fields are used as inputs. Furthermore, we show that our estimations are only slightly affected by the absence of NO2 fields or a detection mechanism as additional information. Finally, interpretability techniques applied to our models confirm that the CNN automatically learns to identify the XCO2 plume and to assess emissions from the plume concentrations. These promising results suggest a high potential of CNNs in estimating local CO2 emissions from satellite images. [ABSTRACT FROM AUTHOR]

As the vegetation in the Arctic changes, tundra ecosystems along the southern border of the Arctic are becoming greener and gradually giving way to boreal ecosystems. This change is affecting local populations, wildlife, energy exchange processes between environmental compartments, and the carbon cycle. To understand the progression and the implications of this change in vegetation, satellite measurements and surface models can be employed. However, in situ observational data are required to validate these measurements and models. This paper presents observational data from two nearby sites in the forest–tundra ecotone in the Tasiapik Valley near Umiujaq in Northern Quebec, Canada. One site is on a mixture of lichen and shrub tundra. The associated data set comprises 9 years of meteorological, soil and snow data as well as 3 years of eddy covariance data. The other site, 850 m away, features vegetation consisting mostly of tall shrubs and black spruce. For that location, 6 years of meteorological, soil and snow data are available. In addition to the data from the automated stations, profiles of snow density and specific surface area were collected during field campaigns. The data are available at 10.1594/PANGAEA.964743 (Domine et al., 2024). [ABSTRACT FROM AUTHOR]

Catalytic synthesis of urea is a bright substitutable to Haber–Bosch progression and industrial urea synthesis. Electrochemical C–N coupling of carbon dioxide and nitrogen oxides under environmental conditions is a newly developed method, which also provides a novel opinion for solving nitrate contamination. Conjugated organic frameworks (COFs) have been used as prospective electrocatalysts for nitrogen reduction reactions and carbon dioxide reduction reactions (CO2RR) as a result of their regulate structure and multihole properties, resulting in efficient electron transfer. This paper reports the efficient synthesis of urea from carbon dioxide and nitrate over MoM1S-Pc-M2PPs COF (M as a transition metal) electrocatalyst. According to the calculation of DFT, it was found that it was difficult for carbon dioxide and nitrogen oxide to coadsorb on MoM1S-Pc to synthesize urea, so we chose to synthesize CO on the metal porphyrin (M2PPs) structural unit, and then overflow on the bimetallic phthalocyanine and nitrogen oxide to synthesize urea. The possibility of nitrate adsorption on different catalysts was verified by calculation. We screened the stability, nitrate adsorption strength, and catalytic activity of MoM1S-Pc candidates, and the results showed that the most promising candidate catalyst was MoFeS-Pc. At the same time, the CO2RR M2PPs substrate was also screened, and the VPPs structure was selected as the best. In the study of coupling between different nitrogen-containing intermediates and *CO, the C–N coupling mechanism shows that *NOH and *CO are two possible C–N coupling nitrogen intermediates, which are shown to be thermodynamically spontaneous and have an inferior activation barrier. This study not only provisions novel perceptions into urea synthesis by coupling nitrogen oxides with carbon dioxide under environmental conditions, but also paves the way for boosting the sustainable production of carbon and nitrogen-coupled products. [ABSTRACT FROM AUTHOR]

The objective of this study is to construct a refined microscopic transport model that elucidates the transport mechanisms of gas flow within micro-nano pores and fractures. The collective impact of various microscopic transport mechanisms was explained through the apparent permeability model, specifically related to gases such as methane and carbon dioxide, within the shale matrix. The apparent permeability models, taking into account microscopic transport mechanisms such as slippage flow, Knudsen diffusion, transition flow, and surface diffusion, were established individually. Subsequently, the influencing factors on apparent permeability were analyzed. The results demonstrate that the apparent permeability of the shale reservoir matrix is significantly influenced by pore pressure, temperature, pore size, and total organic carbon (TOC). As pressure decreases, the apparent permeability of Knudsen diffusion and surface diffusion increases, while the apparent permeability of slippage flow decreases. In addition, the apparent permeability of the reservoir matrix initially decreases and then increases. With increasing temperature, the apparent permeability of slippage flow, Knudsen diffusion, and surface diffusion all increase, as does the apparent permeability of the reservoir matrix. As pore size increases, the apparent permeability of surface diffusion and Knudsen diffusion decreases, while the apparent permeability of slippage flow and the reservoir matrix increases. Furthermore, an increase in TOC leads to no change in the apparent permeability of slippage flow and Knudsen diffusion, but an increase in the apparent permeability of surface diffusion and the reservoir matrix. The model presented in this paper enhances the multi-scale characterization of gas microflow mechanisms in shale and establishes the macroscopic application of these micro-mechanisms. Moreover, this study provides a theoretical foundation for the implementation of carbon capture, utilization, and storage (CCUS) in shale gas production. [ABSTRACT FROM AUTHOR]

Across Europe, countries are reducing CO2 emissions and energy demand by lowering the temperature in public office buildings. These measures affect men and women unequally because the latter prefer and, indeed, perform better under higher temperatures than the standard temperature. Lowering the temperature thus further increases an already existing inequality. We show that the philosophical literature on discrimination provides an interesting theoretical approach to understanding such measures. On prominent understandings of what discrimination is, the policy would be considered direct discrimination against women if it could be shown to reflect a broader inattentiveness to the needs of women in society. Alternatively, and more straightforwardly, the policies can be considered indirect discrimination because of their disparate effects on men and women. The final part of the paper shows that the policies are also wrong for the reasons it is often argued that discrimination is wrong—to wit, that it harms or disrespects those who are discriminated against. The final section suggests a range of measures to offset the discriminatory aspects of the policy. [ABSTRACT FROM AUTHOR]

The Geostationary Carbon Cycle Observatory (GeoCarb) was selected as NASA's second Earth Venture Mission (EVM-2). The scientific objectives of GeoCarb were to advance our knowledge of the carbon cycle, in particular, land–atmosphere fluxes of the greenhouse gases carbon dioxide (CO 2) and methane (CH 4) and the effects of these fluxes on the Earth's radiation budget. GeoCarb would retrieve column-integrated dry-air mole fractions of CO 2 (XCO2), CH 4 (XCH4) and CO (XCO), important for understanding tropospheric chemistry), in addition to solar-induced fluorescence (SIF), from hyperspectral resolution measurements in the O 2 A-band at 0.76 µ m, the weak CO 2 band at 1.6 µ m, the strong CO 2 band at 2.06 µ m, and a CH 4 /CO band at 2.32 µ m. Unlike its predecessors (OCO-2/3, GOSAT-1/2, TROPOMI), GeoCarb would be in a geostationary orbit with a sub-satellite point centered over the Americas. This orbital configuration combined with its high-spatial-resolution imaging capabilities would provide an unprecedented view of these quantities on spatial and temporal scales accurate enough to resolve sources and sinks to improve land–atmosphere CO 2 and CH 4 flux calculations and reduce the uncertainty of these fluxes. This paper will present a description of the GeoCarb instrument and the L2 retrieval algorithms which will be followed by simulation experiments to determine an error budget for each target gas. Several sources of uncertainty will be explored, including that from the instrument calibration parameters for radiometric gain, the instrument line shape (ILS), the polarization, and the geolocation pointing, in addition to forward model parameters including meteorology and spectroscopy, although there are some other instrument-related sources of uncertainty that are left out for this study, including that from "smile", the keystone effect, stray light, detector persistence, and scene inhomogeneity. The results indicate that the errors (1 σ) are less than the instrument's multi-sounding precision requirements of 1.2 ppm, 10 ppb, and 12 ppb (10 %), for XCO2 , XCH4 , and XCO , respectively. In particular, when considering the sources of uncertainty separately and in combination (all sources included), we find overall RMSEs of 1.06 ppm for XCO2 , 8.2 ppb for XCH4 , and 2.5 ppb for XCO , respectively. Additionally, we find that, as expected, errors in XCO2 and XCH4 are dominated by forward model and other systematic errors, while errors in XCO are dominated by measurement noise. It is important to note that the GeoCarb mission was canceled by NASA; however, the instrument is still in development and will be delivered to NASA, in full, with the hope that it will eventually be adopted in a future mission proposal. [ABSTRACT FROM AUTHOR]