Yield Rate Research Articles

Continuous Electrosynthesis of Pure H2O2 Solution with Medical-Grade Concentration by a Conductive Ni-Phthalocyanine-Based Covalent Organic Framework.

Electrosynthesis of H2O2 provides an environmentally friendly alternative to the traditional anthraquinone method employed in industry, but suffers from impurities and restricted yield rate and concentration of H2O2. Herein, we demonstrated a Ni-phthalocyanine-based covalent-organic framework (COF, denoted as BBL-PcNi) with a higher inherent conductivity of 1.14 × 10-5 S m-1, which exhibited an ultrahigh current density of 530 mA cm-2 with a Faradaic efficiency (H2O2) of ∼100% at a low cell voltage of 3.5 V. Notably, this high level of performance is maintained over a continuous operation of 200 h without noticeable degradation. When integrated into a scale-up membrane electrode assembly electrolyzer and operated at ∼3300 mA at a very low cell voltage of 2 V, BBL-PcNi continuously yielded a pure H2O2 solution with medical-grade concentration (3.5 wt %), which is at least 3.5 times higher than previously reported catalysts and 1.5 times the output of the traditional anthraquinone process. A mechanistic study revealed that enhancing the π-conjugation to reduce the band gap of the molecular catalytic sites integrated into a COF is more effective to enhance its inherent electron transport ability, thereby significantly improving the electrocatalytic performance for H2O2 generation.

In situRaman investigation to electrochemical synthesis of ammonia on Pd nanocrystals.

Nitrate and nitrite are widely present in industrial wastewater and domestic sewage, so electrocatalytic reduction of both nitrate and nitrite to ammonia synthesis is considered to be a sustainable development approach. Pd nanostructures have attracted much attention because of their high activity in catalyzing the nitrate electrochemical reduction reaction. Here we prepare Pd nanocube and octahedron for the electrochemical reduction of nitrate and nitrite. It is found that Pd octahedron shows slightly higher activity toward nitrate reduction than Pd nanocube, while for nitrite reduction, Pd octahedron shows much higher activity than Pd nanocube. The ammonia yield rate is more potential-dependent.In situRaman characterization further confirms the existence of adsorbed ammonia on the surface of nanocube and octahedron, indicating similar reduction pathways on (111)-facet octahedron and (100)-facet nanocube.

Electron Deficiency is More Important than Conductivity in C-N Coupling for Electrocatalytic Urea Synthesis.

The electrocatalytic C-N coupling from CO2 and nitrate emerges as one of the solutions for waste upgrading and urea synthesis. In this work, we constructed electron-deficient Cu sites by the strong metal-polymer semiconductor interaction, to boost efficient and durable urea synthesis. In situ Raman spectroscopy identified the existence of electron-deficient Cu sites and was able to withstand electrochemical reduction conditions. Operando synchrotron-radiation Fourier transform infrared spectroscopy and theoretical calculations disclosed the vital role of electron-deficient Cu in adsorption and C-N coupling of oxygen-containing species. The electron-deficient Cu displayed a high urea yield rate of 255.0 mmol h-1 g-1 at -1.4 V versus the reversible hydrogen electrode and excellent electrochemical durability, superior than that of non-electron-deficient counterpart with conductive carbon material as the support. It can be concluded that the regulation of site electronic structure is more important than the optimization of catalyst conductive properties in the C-N coupling reactions.

Electrophoretic deposition of LiFePO4 and carbon black: A numerical study to explore longitudinal trends using Taguchi design

Developing Electrophoretic Deposition (EPD) for Composite Structural Batteries (CSBs) could revolutionise energy storage technology. CSBs offer an innovative solution by seamlessly integrating batteries into structures and effectively reducing weight and space constraints. Despite its successful implementation across various fields, EPD method still lacks comprehensive understanding of the underlying physical and chemical processes due to the number of variables involved. In this study the effects of key parameters associated with the process are investigated with a coupled FEM and analytical approach to find correlations with the deposition process. A Taguchi Design of Experiment with five parameters, namely voltage, concentration, relative weight ratio of LiFePO4 – carbon black particles, length and perimeter of the electrodes is implemented to identify the correlations with mass deposited, thickness of the coating and yield rate when LiFePO4 and Carbon Black particles in ethanol suspension are used. In order to capture the variation over time, each parameter is studied at six different time of deposition. A concentration that optimises yield rate resulting in thickness and mass deposition is identified. The resistivity of the suspension dictates the yield rate dynamics, allowing it to be designed within a specific range to meet requirements of different applications.

Comparative Evaluation of Hematological Parameters and Instrument Performance in Single and Double Plateletpheresis Procedures Using Haemonetics MCS+ and Trima Accel Systems

ObjectivesPlateletpheresis (PP) has become increasingly prevalent due to its cost-effectiveness and fewer immunological and infectious complications for recipients. This study compares hematological indices of platelet donors and instrument-related parameters in high-yield PP donors using Haemonetics MCS+ and Trima Accel. MethodsEligible and healthy PP donors meeting the platelet donation criteria were randomly selected.19 single-dose platelet (SDP), and 26 double-dose platelet (DDP) donors underwent PP using the Haemonetics MCS+, while 21 SDP and 21 DDP donors were processed using the Trima Accel system. Complete Blood Count (CBC) and hematological indices of donors between groups with both devices were measured with the cell counter. Platelet yield, collection efficiency (CE), and collection rate (CR) were evaluated for both devices. Results were reported using R-4.3.2 software and a p-value<0.05 was considered statistically significant ResultsThe Trima Accel processed significantly more blood volume and had shorter procedure times than MCS+. Platelet yield in the SDP group with Trima Accel was significantly higher than the Haemonetics MCS+. The Trima Accel demonstrated a significantly higher CR and CE than the MCS+ in both SDP and DDP groups. Post-PP lymphocyte counts significantly decreased with the Trima compared to the MCS+ in the SDP group. However, post-PP hematocrit (HCT), mean corpuscular volume (MCV), and mean platelet volume (MPV) in the DDP group with the MCS+ were significantly lower than Trima. ConclusionDouble-dose plateletpheresis (DDP) offers advantages in cost-effectiveness and platelet production, and although it reduces some hematological indices, these remain within normal limits. The Trima Accel may offer superior efficiency and processing times compared to the MCS+. However, careful monitoring of DDP donors following AABB standards remains essential.

Drip Fertigation Improves Maize Yield, Resource Utilization, and Economic Benefits by Increasing Light Interception Under Dense Planting in Southwest China

ABSTRACTSeasonal drought and traditional water‐fertilizer management limit the increase in the grain yield of summer maize in Southwest China. Drip fertigation mode (HM) can effectively improve crop yields. However, research on drip fertigation has not been conducted in Southwest China. A 2‐year field experiment about HM was carried out with the traditional water‐fertilizer management mode (FM) as control. The plant densities were 5.25 × 104 plants ha−1 and 8.25 × 104 plants ha−1 in 2022 and 6.00 × 104 plants ha−1 and 9.00 × 104 plants ha−1 in 2023. The effects of HM on the aboveground biomass, leaf area index, yield, and resource utilization rate of summer maize were studied. Compared with the FM treatment, the HM treatment significantly increased the yield (25.18%), aboveground biomass (25.58%), leaf area index (34.87%), and leaf area duration (29.60%). HM optimized the canopy structure with an 11.05% improvement in light transmission at the top and a significant 61.32% increase in cumulative light radiation interception per unit area at the bottom of the canopy. The nitrogen partial factor productivity (NPFP), radiation utilization efficiency (RUE), heat utilization efficiency (HUE), and economic benefits of the HM treatment significantly increased by 39.58%, 49.45%, 25.92%, and 32.53%, respectively. In addition, dense planting increased the irrigation water use efficiency (IWUE) by 14.25%. In summary, drip irrigation combined with water and fertilizer can significantly improve maize grain yield, resource utilization efficiency, and economic benefits by increasing light interception in Southwest China. This study will lay a theoretical foundation for filling the relevant research gap in the region.

Enhancing Compatibility of Two-Step Tandem Catalytic Nitrate Reduction to Ammonia Over P-Cu/Co(OH)2.

Electrochemical nitrate reduction reaction (NO3RR) is a promising approach to realize ammonia generation and wastewater treatment. However, the transformation from NO3 - to NH3 involves multiple proton-coupled electron transfer processes and by-products (NO2 -, H2, etc.), making high ammonia selectivity a challenge. Herein, a two-phase nanoflower P-Cu/Co(OH)2 electrocatalyst consisting of P-Cu clusters and P-Co(OH)2 nanosheets is designed to match the two-step tandem process (NO3 - to NO2 - and NO2 - to NH3) more compatible, avoiding excessive NO2 - accumulation and optimizing the whole tandem reaction. Focusing on the initial 2e- process, the inhibited *NO2 desorption on Cu sites in P-Cu gives rise to the more appropriate NO2 - released in electrolyte. Subsequently, P-Co(OH)2 exhibits a superior capacity for trapping and transforming the desorbed NO2 - during the latter 6e- process due to the thermodynamic advantage and contributions of active hydrogen. In 1m KOH + 0.1m NO3 -, P-Cu/Co(OH)2 leads to superior NH3 yield rate of 42.63mgh- 1cm- 2 and NH3 Faradaic efficiency of 97.04% at -0.4V versus the reversible hydrogen electrode. Such a well-matched two-step process achieves remarkable NH3 synthesis performance from the perspective of optimizing the tandem catalytic reaction, offering a novel guideline for the design of NO3RR electrocatalysts.

High-entropy FeCoNiCuRu solid solutions triggered cocktail effect to achieve fine-tuning adsorption energy for boosting nitrate electroreduction to ammonia

Designing multi-site high-entropy alloys (HEAs) electrocatalysts with fine-tuning adsorption energy range for efficient NO3RR is crucial, but selecting metal elements and clarifying the “cocktail effect” mechanism for NO3RR using HEA solid solutions’ designability remains a challenge. Here, we synthesize FeCoNiCuRu high-entropy alloy (denoted as FeCoNiCuRu HEA) solid solutions as a NO3RR catalyst via a facile one-step solvothermal method. The FeCoNiCuRu HEA catalyst exhibits outstanding NO3RR performance with a maximum NH3 yield rate of 8414.5 μg h−1 cm−2 and a superior Faradaic efficiency of 94.5 %. Significantly, when evaluated in the flow cell, FeCoNiCuRu HEA displays an average Faradaic efficiency of up to 94.5 % and remarkable durability over 45 h. In situ ATR-FTIR, Raman spectroscopy and DFT calculations offer an intensive understanding of the activities of the different metal reaction sites, indicating that the synergistic “cocktail effect” of HEA effectively overcome the high-energy barriers to initial adsorption, enhance adsorption of *H, and suppressed competing HERs, thus facilitating the generation of NH3. This work not only promotes the understanding of the “cocktail effect” of NO3RR performance in the HEA system, but also guides the design/fabrication of advanced HEA electrocatalysts.

A Cu/Fe3O4@CN tandem catalyst for efficient ammonia electrosynthesis from nitrate reduction

Electrochemical nitrate reduction reaction (ENO3RR) is a green technology for value-added ammonia production meanwhile treating waste water at ambient conditions. However, it remains a great challenge to construct efficient catalysts due to the complex multiple proton and electron transfer process. Herein, we report a tandem catalyst Cu/Fe3O4@CN composed of N-doped carbon layer coated Cu/Fe3O4 heterostructure toward highly efficient electrocatalytic nitrate reduction to ammonia production in alkaline medium. The catalyst can achieve an ammonia Faradaic efficiency and ammonia yield rate as high as 96.57 % and 22104.15 μg h−1 mgcat−1 at the optimal potential of −0.9 V vs RHE in 0.1 M KOH. The outstanding ENO3RR performance outperforms the most of reported transitional metal-based ENO3RR electrocatalysts. More importantly, Cu/Fe3O4@CN also exhibits excellent stability even under large current density of 200 mA cm−2, and long-time durability for continuous electrolysis for 36 h. The experimental and theoretical calculations verify the tandem catalysis mechanism of NO3− → NO2− → NH3 through the synergism of the two components Cu and Fe3O4 in Cu/Fe3O4@CN. Specifically, Cu has strong NO3− adsorption capacity which can be reduced into NO2−, while Fe3O4 can boost water dissociation to generate abundant active *H, ensuring the smooth hydrogenation process while suppressing the occurrence of competitive hydrogen evolution reactions (HER). The heterostructure formation between Cu and Fe3O4 also significantly reduces the energy barrier of the rate-determining step (*NO → *NOH), which results in the high performance of Cu/Fe3O4@CN.

Mechanism of heterogeneous substrate stimulating growth for nickel-based single crystal superalloy

Minimizing the deviation of single-crystal (SX) primary orientation can significantly enhance the yield rate, service life, and performance of turbine blades or castings. Substrate stimulating method controls the deviation of <001> orientation within a narrower range by inducing nucleation of specific crystalline planes. In this study, during heterogeneous substrate stimulating growth for DD5 superalloy, the mechanism by which lattice misfit influences the orientation of new crystals were systematically elucidated. The study variables include substrate materials ((001) SX DD5, polycrystal DD5, and polycrystal Cu), orientations ((001), (101), (111)), cooling rates, and temperature. The target oriented grains were increased when the lattice misfit between the substrates of varying materials or orientations and new crystal were minimized. The melt undercooling decreases as the substrate cooling rate decreases, which can only stimulate the nucleation of crystalline planes with lower energy barriers (characterized by minimal lattice misfit). The thermal gradient in the melt decreases and the lattice misfit simultaneously decreases as the substrate temperature increases, these two factors jointly contribute to stimulating grains with lower lattice misfit. The substrate temperature leads to more pronounced variation in the proportion of target grains, than does the substrate cooling rate.

A Newly Predicted Magnetic TMB6 Monolayer for Efficient Nitrogen Fixation.

Developing electrocatalysts for the N2 reduction reaction (NRR) with high activity, high selectivity, and low cost is urgently required to enhance the NH3 yield rate. Based on first-principles calculations, we predict a series of new transition metal boride TMB6 (TM = Ti, V, Cr, Mn, Fe, and Co) monolayers and investigate their magnetoelectronic and electrocatalytic properties. The results reveal that VB6 and CoB6 favor ferromagnetic coupling, while TiB6, CrB6, MnB6, and FeB6 display antiferromagnetic ordering. Furthermore, TiB6 exhibits a high Néel temperature of 344 K and a large magnetic anisotropy energy of 614 μeV per Ti atom. Most interestingly, TiB6 and VB6 exhibit superior NRR catalytic activity with a limiting potential of -0.50 and -0.19 V, respectively, and favorable NRR selectivity over the HER. Finally, the structural stability of TMB6 monolayers has been confirmed by a set of phonon dispersion, molecular dynamics, and elastic constant calculations. Our results highlight the use of the newly designed two-dimensional (2D) TM borides as promising candidates for spintronic devices and nitrogen fixation applications.

Harvesting Zr-based metal-organic frameworks by continuous-flow synthesis as efficient adsorbents for eliminating nitrogen-containing compounds in liquid fuel

This work designed a continuous-flow tubular reactor for rapidly and scalably harvesting the metal-organic framework (MOF) of UiO-66(Zr)-NH2. The experimental conditions, including temperature (110–140 °C), holding time (10–30 min), and CH3COOH/H2N-BDC molar ratio (100–250), were carried out to survey their impacts on the product yield and quality. The highest yield and production rate of ∼72% and ∼1.55 g h−1 were obtained at 130 °C, 20 min, and CH3COOH/H2N-BDC ratio 200. The temperature and modulator content significantly influenced MOFs’ crystal morphology, crystallinity, and porosity. Besides, the adopted method also successfully produced UiO-66 and UiO-67 MOFs with high production rates. The adsorptive denitrogenation (ADN) performances were carried out using liquid fuel models containing quinoline (QU) and 2-methyl pyrrole (MP). In batch mode adsorption, the UiO-66-NH2-130-200 sample showed the highest adsorbing quantities of ∼199 and ∼163 mg g−1 for QU and MP, respectively. Furthermore, the prepared MOFs efficiently removed NCCs from liquid fuel under a continuous fixed-bed column process. These demonstrate that modulator-assisted continuous-flow synthesis can be a potential strategy for the scalable harvest of Zr-MOFs with good qualities and high performance in getting rid of NCCs from liquid fuel.

Additional Diagnostic Yield of the Rapid Drink Challenge in Chicago Classification Version 4.0 Compared With Version 3.0.

Chicago classification version 4.0 enhances the diagnosis of esophageal motility disorders using position change and provocative tests such as multiple rapid swallows and a rapid drink challenge. This study investigates the diagnostic role of the rapid drink challenge based on Chicago classification 4.0 using a functional luminal imaging probe to estimate the cutoff value. This study included 570 patients who underwent esophageal manometry with a rapid drink challenge between January 2019 and October 2022. The diagnostic flow was analyzed according to Chicago classification 4.0. Ninety-nine patients (38, achalasia; 11, esophagogastric junction outflow obstruction; 7, ineffective esophageal motility; 1, hypercontractile esophagus; and 42, normal esophageal function) failed the rapid drink challenge. Among the 453 participants, 50 and 86 were diagnosed with achalasia and esophagogastric junction outflow obstruction, respectively, using Chicago classification 4.0. In 249/453 (55.0%) patients initially diagnosed with esophagogastric junction outflow obstruction using Chicago classification 3.0, the diagnosis was changed to achalasia (n = 28), hypercontractile esophagus (n = 7), ineffective esophageal motility (n = 7), or normal esophageal function (n = 121) using Chicago classification 4.0. Rapid drink challenge-integrated relaxation pressure's diagnostic cutoff value was 19 mmHg. Nine patients had diagnoses changed after the rapid drink challenge, including 3 with panesophageal pressurization. Chicago classification 4.0 increased the diagnostic yield of the rapid drink challenge by 2.0% (9/453 patients). However, the rapid drink challenge had a failure rate of 17.9% (99/552 patients). Given the relatively low diagnostic yield and high failure rate of the rapid drink challenge, we recommend adopting an individualized approach to manometry.

Accelerated Proton-Coupled Electron Transfer via Engineering Palladium Sub-Nanoclusters for Scalable Electrosynthesis of Hydrogen Peroxide.

Electrosynthesis of H2O2 from oxygen reduction reaction via a two-electron pathway is vital as an alternative for the energy-intensive anthraquinone process. However, this process is largely hindered in neutral and alkaline conditions due to sluggish kinetics associated with the transformation of intermediate O2* into OOH* via proton-coupled electron transfer sourced from slow water dissociation. Herein, we developed Pd sub-nanoclusters on the nickel ditelluride nanosheets (Pd SNCs/NiTe2) to enhance the performance of H2O2 electrosynthesis. The newly-developed Pd SNCs/NiTe2 exhibited a H2O2 selectivity of as high as 99 % and a positive shift of onset potential up to 0.81 V. Combined theoretical calculations and experimental studies (e.g., X-ray absorption and attenuated total reflectance-Fourier transform infrared spectra measurements) revealed that the Pd sub-nanoclusters supported by NiTe2 nanosheets efficiently reduced the energy barrier of water dissociation to generate more protons, facilitating the proton feeding kinetics. When used in a flow cell, Pd SNCs/NiTe2 cathode efficiently produced H2O2 with a maximum yield rate of 1.75 mmol h-1 cm-2 and a current efficiency of 95 % at 100 mA cm-2. Further, an accumulated H2O2 concentration of 1.43 mol L-1 was reached after 10 hours of continuous electrolysis, showing the potential for practical H2O2 electrosynthesis.

Accelerated Proton‐Coupled Electron Transfer via Engineering Palladium Sub‐Nanoclusters for Scalable Electrosynthesis of Hydrogen Peroxide

AbstractElectrosynthesis of H2O2 from oxygen reduction reaction via a two‐electron pathway is vital as an alternative for the energy‐intensive anthraquinone process. However, this process is largely hindered in neutral and alkaline conditions due to sluggish kinetics associated with the transformation of intermediate O2* into OOH* via proton‐coupled electron transfer sourced from slow water dissociation. Herein, we developed Pd sub‐nanoclusters on the nickel ditelluride nanosheets (Pd SNCs/NiTe2) to enhance the performance of H2O2 electrosynthesis. The newly‐developed Pd SNCs/NiTe2 exhibited a H2O2 selectivity of as high as 99 % and a positive shift of onset potential up to 0.81 V. Combined theoretical calculations and experimental studies (e.g., X‐ray absorption and attenuated total reflectance‐Fourier transform infrared spectra measurements) revealed that the Pd sub‐nanoclusters supported by NiTe2 nanosheets efficiently reduced the energy barrier of water dissociation to generate more protons, facilitating the proton feeding kinetics. When used in a flow cell, Pd SNCs/NiTe2 cathode efficiently produced H2O2 with a maximum yield rate of 1.75 mmol h−1 cm−2 and a current efficiency of 95 % at 100 mA cm−2. Further, an accumulated H2O2 concentration of 1.43 mol L−1 was reached after 10 hours of continuous electrolysis, showing the potential for practical H2O2 electrosynthesis.

Optimization of the Thermokinetic Method for the Control of Weld Decay in AISI 304L and AISI 316L Stainless Steel Weldment

This study investigates the control of weld decay in AISI 304L/316L alloy weldments for liquefied natural gas (LNG) and cryogenic environments using the Tungsten Inert Gas (TIG) welding technique. Weldment samples were thermokinetically treated at 1050, 1100, and 1150°C and cooled in five mediums: Water, Salt, Natural Air, Salt with annealing, and Water with annealing, to retain carbon and chromium in solid solution at approximately 30°C. Furthermore, evaluation methods based on metallography i.e. optical microscopy (OM), Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray Spectroscopy (EDX), Wear Test (i.e. wear rate and wear track) and electrochemical corrosion potential measurements were adopted. An experimental design table was developed using the design expert software 13.0. This helped develop a predictive mathematical model for ascertaining the optimum operating service conditions of the material. From the results, the optical microscopy analysis revealed that the control sample exhibited a more irregular pattern than others. Results showed that the control sample had a more irregular structure, while air-cooled samples exhibited smoother surfaces, indicating better bonding. SEM revealed a coarse surface with uneven particle distribution post-heat application. The predominant elements were Iron (Fe), Chromium (Cr), and Nickel (Ni). Corrosion potential varied between -0.5 to 0.15 V, demonstrating wave-like behaviour over time. Wear analysis indicated that lower coefficients of friction correlate with better wear resistance. Finally, response surface methodology (RSM) revealed that increasing temperature proportionally increased yield and corrosion rates. While the identified optimal values for Temperature are (1112.68°C), Material (316L), and Quenching Medium (SQ+SA), resulting in specific values such as Wear Rate (5.76896E-06), Coefficient of friction (0.224254), Corrosion Rate (0.395566), and Weight of Heat-Treated Sample (14.7797). The study enhances understanding of the mechanisms affecting welding and contributes to optimizing welding procedures for improved mechanical properties and corrosion resistance.

A Strongly Coupled Metal/Hydroxide Heterostructure Cascades Carbon Dioxide and Nitrate Reduction Reactions toward Efficient Urea Electrosynthesis.

The direct coupling of nitrate ions and carbon dioxide for urea synthesis presents an appealing alternative to the Bosch-Meiser process in industry. The simultaneous activation of carbon dioxide and nitrate, however, as well as efficient C-N coupling on single active site, poses significant challenges. Here, we propose a novel metal/hydroxide heterostructure strategy based on synthesizing an Ag-CuNi(OH)2 composite to cascade carbon dioxide and nitrate reduction reactions for urea electrosynthesis. The strongly coupled metal/hydroxide heterostructure interface integrates two distinct sites for carbon dioxide and nitrate activation, and facilitates the coupling of *CO (on silver, where * denotes an active site) and *NH2 (on hydroxide) for urea formation. Moreover, the strongly coupled interface optimizes the water splitting process and facilitates the supply of active hydrogen atoms, thereby expediting the deoxyreduction processes essential for urea formation. Consequently, our Ag-CuNi(OH)2 composite delivers a high urea yield rate of 25.6 mmol gcat. -1 h-1 and high urea Faradaic efficiency of 46.1 %, as well as excellent cycling stability. This work provides new insights into the design of dual-site catalysts for C-N coupling, considering their role on the interface.

Effect of CO2 injection pressure on enhanced coal seam gas extraction

The CO2 displacement of coal seam gas can simultaneously promote gas extraction and CO2 sequestration, with gas injection pressure being a key factor influencing both efficiency and safety. This study examined the impact of varying CO2 injection pressure on gas extraction and sequestration. The findings indicated that higher CO2 injection pressures reduced the gas injection and extraction time costs, increased the equilibrium pressure and coal seam temperature, and decreased carbon sequestration efficiency. As the CO2 injection pressure increased, the CH4 cumulative desorption capacity and desorption rate rose by 4.98%, the time to reach the residual gas content critical value (TLV of 2 m3/t) shortened by 62.04 min, and the maximum CO2 storage per unit mass of coal increases by 3.6 m3/t. Increasing the injection pressure enhanced gas desorption and CO2 sequestration. A higher CO2 injection pressure resulted in a higher CH4 yield rate and a reduced CO2 injection rate in the later stages. Therefore, it is advisable to reduce the CO2 injection pressure during the low efficiency desorption stage.

A Strongly Coupled Metal/Hydroxide Heterostructure Cascades Carbon Dioxide and Nitrate Reduction Reactions toward Efficient Urea Electrosynthesis

AbstractThe direct coupling of nitrate ions and carbon dioxide for urea synthesis presents an appealing alternative to the Bosch–Meiser process in industry. The simultaneous activation of carbon dioxide and nitrate, however, as well as efficient C−N coupling on single active site, poses significant challenges. Here, we propose a novel metal/hydroxide heterostructure strategy based on synthesizing an Ag−CuNi(OH)2 composite to cascade carbon dioxide and nitrate reduction reactions for urea electrosynthesis. The strongly coupled metal/hydroxide heterostructure interface integrates two distinct sites for carbon dioxide and nitrate activation, and facilitates the coupling of *CO (on silver, where * denotes an active site) and *NH2 (on hydroxide) for urea formation. Moreover, the strongly coupled interface optimizes the water splitting process and facilitates the supply of active hydrogen atoms, thereby expediting the deoxyreduction processes essential for urea formation. Consequently, our Ag−CuNi(OH)2 composite delivers a high urea yield rate of 25.6 mmol gcat.−1 h−1 and high urea Faradaic efficiency of 46.1 %, as well as excellent cycling stability. This work provides new insights into the design of dual‐site catalysts for C−N coupling, considering their role on the interface.

Predicting well productivity in cratonic regions using remote sensing lineaments and weathered cover thickness: A case study from Bobo Dioulasso, Burkina Faso

In western African cratonic regions, fractured crystalline bedrock, Neoproterozoic sedimentary covers, and regolith deposits constitute the most productive aquifer systems. Structural lineaments derived from remote sensing data and weathered cover thickness from borehole interpretations provide cost-effective methods for evaluating well productivity in regions with limited economic resources and hydrogeological knowledge, such as Houet province in Western Burkina Faso. Structural lineaments were interpreted using 1:200,000 Landsat TM images and 1:50,000 aerial photographs, revealing NE and NW as the most significant directions. An analysis of 101 borehole stratigraphic profiles from rural water supply program reports revealed the weathering depth and cover thickness. Borehole productivity exhibited a strong correlation with increased weathered cover thickness. Negative well results were concentrated in areas with less than 5 m of cover. In contrast, significant differences in specific yield rates were observed with greater thicknesses, ranging from 2.5 m³/d for 20 m of saturated thickness to 7.6 m³/d when the regolith reached a depth of 40 m. These preliminary groundwater exploration tools effectively target successful well sites by accounting for differing lithologies, regional tectonics, and regolith development. This approach is particularly relevant for cratonic regions with limited resources and hydrogeological knowledge, aiding in sustainable groundwater development and land-use planning.