Capture Performance Research Articles

Novel chitosan-based derivative material loaded with the diethylenetriamine pentamethylene phosphonic acid for efficient adsorption of uranyl ions from weakly acidic wastewater

An ideal adsorption material capable of efficiently and selectively capture uranyl ions from radioactive wastewater remains a serious challenge. In this work, diethylenetriamine pentamethylene phosphonic acid (DTPMP), one of the common metal ion extractants with five negatively charged phosphate groups, was innovatively used to modify chitosan chains for better uranyl adsorption capacity. Two chitosan derivatives were designed, DTPMP protonated chitosan crosslinked with potassium tripolyphosphate (DTPP) and DTPMP reinforced potassium tripolyphosphate crosslinked chitosan (DCTPP), in which DCTPP possessed an excellent maximum adsorption capacity of up to 1316.82 mg/g for uranyl ions at 298 K. Compared to the 60 min taken-for 90 % by DTPP, the time taken to reach same percentage by DCTPP was only about 5 min, indicating its superior uranyl removal efficiency. Outstanding affinity and capture performance could be attributable to the remarkable mesoporous surfaces and abundant P-containing active sites. Influence of initial solution pH on the removal efficiency for uranyl was significantly attenuated due to the C-P bond. The fitting results of kinetic and isotherm models revealed that the uranyl adsorption mechanisms by as-prepared composites were physicochemical processes, mainly including surface complexation/chelation, chemisorption, and intra-particle diffusion. Theory calculations predicted potential binding modes and electrons transfer between the organophosphonic acid molecule and uranyl unit, validating the strong interaction and reduction of phosphorus-oxygen groups on uranyl ions. Furthermore, DCTPP showed great potentials to separate uranyl from simulated uranium-contaminated wastewater. Design and development of novel chitosan derivatives will provide theoretical support and technical reference for an effective treatment of weakly acidic radioactive wastewater.

Highly efficient capture of CO2 through the synergy of intramolecular amines within piperazine‐derived alcoholamines

AbstractAmine‐scrubbing‐based chemical absorption remains a prominent CO2 capture process. However, the overall efficiency of conventional amine absorbents is hard to meet the ever‐increasing demands for CO2 capture. Consequently, developing powerful absorbents for efficient and cost‐effective CO2 capture is greatly important but challenging. Here, a new type of amine absorbent with improved solubility and stability was achieved by substituting the secondary amino groups in piperazine (PZ) with aminoethyl and hydroxyalkyl moieties. The developed amine absorbent presents superior CO2 absorption/desorption abilities through the synergy of their intramolecular amines, leading to a low regeneration energy consumption of 2.56 GJ·t−1 CO2. Moreover, the enhancement of CO2 capture and the corresponding mechanism were elucidated using density functional theory calculations and nuclear magnetic resonance analysis. Such newly developed amine absorbent with excellent CO2 capture performance are expected to greatly contribute to ongoing efforts toward carbon neutrality.

Sustainable and economical alternatives to fragment capture materials in explosive and ballistic trials.

Strawboard has been utilised as a fragmentation capture material since the 1960s, mainly employed to capture fragments from explosives and explosive devices from arena trials of munitions. As this material has historically been calibrated to a known standard, it has a proven record of allowing research establishments to ascertain the velocity of a fragment based on the depth of penetration of the strawboard. During the time of calibration, strawboard was used as a common building material which was both widely available and relatively affordable; however, due to the recent economic crisis and geopolitical supply issues, this is no longer the case. Building on initial testing, this paper investigates alternatives to strawboard to determine if a cheaper, more readily available material can be used instead. The alternatives are compared and judged based on the NATO ARSP-03 guideline for capture material which includes metrics such as price and attainability, as well as assessing environmental impact and its ability to be used as a viable alternative to strawboard in an explosive environment. Based on these NATO guidelines, explosive fragmentation and ballistic experiments were conducted, and ten materials were tested based on the following criteria: Handling, Density, Flammability, Calibration, Cost and Availability. Medium Density Fibreboard (MDF) was found to be a suitable alternative to strawboard. The data demonstrates that it provides the same capture performance as strawboard at approximately a quarter of the cost and is far more readily available. Other materials also showed potential and further testing should be undertaken to validate these materials as alternatives to MDF.

Amine-functionalized high-surface-area Al2O3 adsorbent for CO2 capture: Effect of the support calcination conditions

Porous alumina has garnered interest as a substrate in the development of solid amine adsorbents for CO2 capture. However, the calcination conditions of alumina can significantly alter its properties, which in turn affects the adsorption performance of the resulting adsorbents. In this study, high-surface-area alumina was synthesized using a reverse microemulsion method. The impact of the calcination conditions on the pore structure and surface properties of the alumina precursor was examined. Additionally, the porous alumina produced under various calcination conditions served as the support for tetraethylenepentamine (TEPA) loading, and the CO2 capture performance of the resultant adsorbents was assessed. The adsorption kinetics and activation energy were analyzed, emphasizing the cyclic stability when regenerated in a realistic CO2 atmosphere. Our findings indicate that alumina calcined under an air atmosphere with a lid exhibited the highest capture capacity (reaching 89.97 mg/g after a 40 wt% TEPA loading), compared to other alumina samples. The adsorption kinetics corresponded closely with the Avrami model, yielding an activation energy (Ea) of 4.75 kJ/mol. Both alumina samples calcined in air, with and without a lid, demonstrated robust cycling stability and resistance to urea formation. The underlying anti-urea mechanisms were also elucidated in the study.

Lignin-impregnated biochar assisted with microwave irradiation for CO2 capture: adsorption performance and mechanism

Bamboo biochar was modified by lignin impregnation and microwave irradiation to enhance its performance for CO2 capture. The pore structure of lignin-impregnated biochar was significantly affected by the impregnation ratio. The maximum specific surface area of 377.32 m2 g−1 and micropore volume of 0.163 cm3 g−1 were observed on the biochar with an impregnation ratio of 1:20 (mass ratio of lignin to biochar). Lignin impregnation increased the CO2 adsorption capacity of biochar up to 134.46 mg g−1. Correlation analysis confirmed the crucial role of biochar’s pore structure in adsorption. The Avrami model fitted the CO2 capture curves well. The calculation of adsorption activation energy suggested that the adsorption process was dominated by physical mechanism assisted with partial chemical mechanism. Meanwhile, Langmuir isotherm analysis indicated that lignin impregnation transformed the larger pores of biochar into more uniform micropores, thereby making the adsorption process closer to monolayer adsorption. Both the high reusability (89.79–99.06%) after 10 successive cycles and the excellent CO2 selectivity in competitive adsorption confirmed that lignin-impregnated biochar is an outstanding adsorbent for CO2 capture.Graphical

Efficient CO2 capture and separation in TpPa COFs: Synergies from functional groups and metal Li

Covalent organic frameworks (COFs) have emerged as promising materials for CO2 capture and separation owing to their exceptional structural stability. Herein, grand canonical Monte Carlo simulation (GCMC) and density functional theory (DFT) were used to first screen the most favorable functional group in the COFs consisting of 1,3,5-triformylphloroglucinol (Tp) and p-phenylenediamine (Pa) functionalized with –OH, –COOH, and –SO3H, respectively (TpPa-X). Subsequently, the H atoms of –SO3H, the best functional group, were replaced by Li atoms to form –SO3Li, revealing the synergies of functional group –SO3H and Li modification on selective CO2 capture. TpPa-OLi/COOLi were also constructed to confirmed the universality of this synergistic effect. The introduction of functional groups enhanced the CO2 capture and separation performances by creating a more suitable pore environment. The Li introduction increased the structural polarity and provided strong adsorption sites, further improving the selective CO2 capture performance. Notably, TpPa-SO3Li exhibited a remarkable CO2 adsorption capacity of 136.11 cm3 cm−3 with the CO2 over N2/CH4 selectivity of 264.22/164.38, respectively, at 298 K and 1.0 bar. Structural stabilities, pore characteristics, gas adsorption distribution, isothermal adsorption heat, and interactions were adopted to reveal the synergistic effect between functional groups and Li in enhancing CO2 capture and separation.

Integrated experimental and theoretical studies for unravelling CO2 capture of dual function CeO2-CaO bio-based sorbents

Solid CaO-based sorbents for CO2 capture represent a promising alternative technology compared to traditional amine scrubbing methods. However, CaO-based sorbents are rapidly sinter and easily decrease CO2 uptake capacity with regenerated carbonation–calcination cycle. Thus, in this study, doping CaO with CeO2 make it an excellent candidate for improving stability and facilitating CO2 capture efficiency. The dual function of CaO bio-based sorbents with varying ratios of cerium (Ce) were derived from naturally occurring blood clam using the gel-combustion method. Their nanostructures and physicochemical properties were characterized through the specific methods, including in situ XAS, CO2 chemisorption and physisorption, XPS, XRD, and SEM. An in-depth understanding of CO2 adsorption mechanism was further emphasized using a density functional theory (DFT) simulation. The results demonstrate that nanosized CeO2-CaO, with a mole ratio of 1:9, exhibited the highest performance for CO2 capture (6.44 mmol CO2/g sorbent). It is postulated that Ce serves as a physical barrier, effectively partitioning adjacent CaO grains and thereby diminishing the sintering rate. CaO is identified as the primary adsorption site, in contrast to CeO2. Mixing the Ce-Ca dual oxide initiates the electron-rich O at the O’ site. The electron localization at the O’ active site improves the activity of O’, making the performance CeCa(200) for capturing CO2 capture dominant. This discovery suggests that CeO2-CaO holds promise as a sustainable alternative sorbent for future CO2 capture applications.

One-pot preparation of magnetic composite containing boronic acid groups and aminated multwalled carbon nanotubes for the speciation of Se(IV) and Se(VI) in water and milk samples by combination with chromatographic quantification

Speciation of Se(IV) and Se(VI) is essential due to their significant differences in reactivity, toxicity and bioavailability. Efficient extraction is the pivotal step in the quantification of inorganic selenium species. In this work, a new magnetic nano-composite (MNC) containing boronic acid group and aminated multwalled carbon nanotubes was facilely fabricated by means of one-pot hydrothermal strategy. The prepared MNC contained abundant functional groups and satisfactory magnetic saturation value. Combining with magnetic solid phase extraction (MSPE) format, the MNC displayed satisfactory capture performance towards the complex formed by the coordination of Se(IV) and o-phenylenediamine (OPA). Adsorption isotherm and adsorption kinetics were studied in detail to investigate the adsorption procedure of Se(IV)/OPA complex on MNC. Under the optimal preparation conditions of MNC and extraction parameters, the MNC/MSPE was connected with HPLC equipped with a diode array detector (DAD) to quantify trace Se(IV) and Se(VI) species in water and milk samples. Se(VI) was reduced to Se(IV) and then the total inorganic Se was quantified by the developed method. Subtraction method was used to measure the concentration of Se(VI). The achieved limits of detection were in the ranges of 0.0082–0.013 μg/L and 0.041–0.13 μg/kg for water and milk samples, respectively. Recoveries in actual samples spiked with different amounts of analytes varied from 81.0 % and 117 %, and the RSDs for repeatability varied from 1.0 % to 10 %. In comparison with existing studies based on MSPE, the established method presents some merits such as greenness in the preparation of magnetic adsorbent, rapid extraction procedure, low cost and satisfactory sensitivity in the speciation of inorganic Se species.

N-doped hierarchically porous carbons prepared with the assistance of chemical blowing and in-situ hard template as highly efficient CO2 adsorbents: A combined experimental and theoretical study

In the current work, we presented the synthesis of N-doped hierarchically porous carbons (NDHPCs) through chemical activation of hierarchically structured precursor derived from polyvinylpyrrolidone (PVP) and magnesium acetate tetrahydrate. Magnesium acetate tetrahydrate served as the blowing agent, and its decomposition product MgO served as the in-situ formed hard template. Combined with KHCO3 activation, the NDHPCs demonstrated a unique micro-meso-macroporous structure. Owing to the highly porous structure (1560–2545 m2/g) and enriched N-doping (1.48–6.31 wt%), the NDHPCs were investigated as potential CO2 adsorbents in both post-combustion capture and pre-combustion capture applications. When the adsorption temperature was 25 °C, the samples showed outstanding capture performances at both 1 bar (2.97–3.88 mmol/g) and 20 bar (13.24–19.89 mmol/g). The adsorption performances were further analyzed with grand canonical Monte Carlo (GCMC) simulation. Effects of various physicochemical properties on CO2 adsorption at different pressures were thus revealed with a combined experimental-theoretical approach.

High-Capacity, Cooperative CO2 Capture in a Diamine-Appended Metal-Organic Framework through a Combined Chemisorptive and Physisorptive Mechanism.

Diamine-appended Mg2(dobpdc) (dobpdc4- = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate) metal-organic frameworks are promising candidates for carbon capture that exhibit exceptional selectivities and high capacities for CO2. To date, CO2 uptake in these materials has been shown to occur predominantly via a chemisorption mechanism involving CO2 insertion at the amine-appended metal sites, a mechanism that limits the capacity of the material to ∼1 equiv of CO2 per diamine. Herein, we report a new framework, pip2-Mg2(dobpdc) (pip2 = 1-(2-aminoethyl)piperidine), that exhibits two-step CO2 uptake and achieves an unusually high CO2 capacity approaching 1.5 CO2 per diamine at saturation. Analysis of variable-pressure CO2 uptake in the material using solid-state nuclear magnetic resonance (NMR) spectroscopy and in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) reveals that pip2-Mg2(dobpdc) captures CO2 via an unprecedented mechanism involving the initial insertion of CO2 to form ammonium carbamate chains at half of the sites in the material, followed by tandem cooperative chemisorption and physisorption. Powder X-ray diffraction analysis, supported by van der Waals-corrected density functional theory, reveals that physisorbed CO2 occupies a pocket formed by adjacent ammonium carbamate chains and the linker. Based on breakthrough and extended cycling experiments, pip2-Mg2(dobpdc) exhibits exceptional performance for CO2 capture under conditions relevant to the separation of CO2 from landfill gas. More broadly, these results highlight new opportunities for the fundamental design of diamine-Mg2(dobpdc) materials with even higher capacities than those predicted based on CO2 chemisorption alone.

NaNO3-Promoted MgO-Based Adsorbents Prepared from Bischofite for CO2 Capture: Experimental and Density Functional Theory Study.

MgO has broad application potential in CO2 capture at intermedium temperatures. In this paper, the effects of NaNO3 doping on the properties of MgO prepared by using waste bischofite as the raw material were investigated to improve the performance of the CO2 capture. MgO-doped NaNO3 exhibited excellent CO2 capture performance at 320 °C with a maximum adsorption capacity of 36.62 wt %. MgO-doped NaNO3 has good cycling stability after 10 adsorption-desorption cycle experiments. In addition, CO2 adsorption on pure MgO and MgO-NaNO3 surfaces was investigated in accordance with density functional theory. Calculation results show that doping with NaNO3 allows more electrons to be transferred from the MgO substrate to the CO2 molecule. MgO-doped NaNO3 can lead to an increase in adsorption energy, resulting in a more stable structure after adsorption and thereby promoting adsorption. The result of this study provides an effective method for the comprehensive utilization of salt lake resources.

Advanced process integration and machine learning-based optimization to enhance techno-economic-environmental performance of CO2 capture and conversion to methanol

Developing economically sustainable CO2 capture and conversion processes is essential to realize carbon neutrality. This study proposed an integrated process for CO2 capture and conversion-to-methanol (CCTM) and applied machine learning-based optimization to enhance techno-economic-environmental performance. After validating CO2 capture and CO2-to-methanol sections, an advanced CCTM design was developed and compared with conventional one regarding techno-economic-environmental performance across various operating scenarios. The advanced CCTM exhibited significant improvements in energy consumption (14.73–16.30%), production cost (0.81–1.28%), and net CO2 reduction (3.13–3.38%) owing to efficiently reusing waste heat, off-gas, and water resources. The one-at-a-time sensitivity analysis revealed roles of each variable and nonlinear variable-performance tendencies among operating variables in the advanced CCTM process. Subsequently, a well-developed deep neural network (DNN) model precisely formulated the relationship between key variables and performances. The DNN-based optimization provided optimum operating conditions within a minute, resulting in an 8.21 $/tMeOH (∼0.81%) reduction in production cost compared to base case of CCTM. Notably, the total CO2 capture rate of 92.53% at an optimal condition highlighted the significant contribution of advanced CCTM to carbon neutrality. The findings provide a viable reference for the effective and sustainable design and operation of an integrated CCTM process.

The Treatment of Natural Calcium Materials Using the Supercritical Antisolvent Method for CO2 Capture Applications

The potential of the supercritical antisolvent micronization (SAS) technique was evaluated for the production of CaO-based particles with a size and a physical structure that could enable high performance for CO2 capture through the calcium looping process. Two sources of calcium derivative compounds were tested, waste marble powder (WMP) and dolomite. The SAS micronization of the derivate calcium acetate was carried out at 60 °C, 200 bar, a 0.5 mL min−1 flow rate of liquid solution, and 20 mg mL−1 concentration of solute, producing, with a yield of more than 70%, needle-like particles. Moreover, since dolomite presents with a mixture of calcium and magnesium carbonates, the influence of the magnesium fraction in the SAS micronization was also assessed. The micronized mixtures with lower magnesium content (higher calcium fraction) presented needle-like particles similar to WMP. On the other hand, for the higher magnesium fractions, the micronized material was similar to magnesium acetate micronization, presenting sphere-like particles. The use of the micronized material in the Ca-looping processes, considering 10 carbonation-calcination cycles under mild and realistic conditions, showed that under mild conditions, the micronized WMP improved CaO conversion. After 10 cycles the micronization, WMP presented a conversion 1.8 times greater than the unprocessed material. The micronized dolomite, under both mild and real conditions, maintained more stable conversion after 10 cycles.

Research on CO2 capture performance and reaction mechanism using newly tetraethylenepentamine (TEPA) + monoethanolamine (MEA) mixed absorbent for onboard application

Large–scale CO2 emissions have raised international concerns as they lead to global temperature rise. Consequently, mitigating CO2 emissions has emerged as a central focus of interdisciplinary research. Although onboard carbon capture technology proves effective in reducing a ship's CO2 emissions, challenges persist in the form of high desorption energy consumption and low CO2 loading of the absorbents. In this study, a novel polyamine–based mixed amine system based on marine engine exhaust CO2 capture technology has been developed to reduce desorption energy consumption and enhance CO2 loading. Additionally, the reaction mechanisms of CO2 with polyamine–based mixed amine were investigated using a combination of quantum chemical calculations and nuclear magnetic resonance (NMR) techniques. The results indicated that compared to monoethanolamine (MEA) with the same mass fraction, the CO2 loading of the new mixed absorbent tetraethylenepentamine (TEPA) + MEA increased by 7 % and the desorption heat duty reduced by 18.1 %. The analytical approach results showed that in the case of 7.5 wt% TEPA + 7.5 wt% MEA solution, proton transfer was predominantly governed by TEPA, whereas MEA primarily engaged in the reaction with CO2. During desorption at 368 K, the released CO2 primarily arose from HCO3− and CO32−. These findings hold academic and practical significance for the advancement of more efficient carbon capture technologies in maritime applications.

Obesity-Specific Considerations for Assessing Gait with Inertial Measurement Unit-Based vs. Optokinetic Motion Capture.

Adults with obesity experience high rates of disability and rapid functional decline. Identifying movement dysfunction early can direct intervention and disrupt disability development; however, subtle changes in movement are difficult to detect with the naked eye. This study evaluated how a portable, inertial measurement unit (IMU)-based motion capture system compares to a laboratory-based optokinetic motion capture (OMC) system for evaluating gait kinematics in adults with obesity. Ten adults with obesity performed overground walking while equipped with the OMC and IMU systems. Fifteen gait cycles for each participant were extracted for the 150 total cycles analyzed. Kinematics were compared between OMC and IMU across the gait cycles (coefficient of multiple correlations), at clinically significant time points (interclass correlations), and over clinically relevant ranges (Bland-Altman plots). Sagittal plane kinematics were most similar between systems, especially at the knee. Sagittal plane joint angles at clinically meaningful timepoints were poorly associated except for ankle dorsiflexion at heel strike (ρ = 0.38) and minimum angle (ρ = 0.83). All motions except for ankle dorsiflexion and hip abduction had >5° difference between systems across the range of angles measured. While IMU-based motion capture shows promise for detecting subtle gait changes in adults with obesity, more work is needed before this method can replace traditional OMC. Future work should explore standardization procedures to improve consistency of IMU motion capture performance.

Deep learning and big data mining for Metal–Organic frameworks with high performance for simultaneous desulfurization and carbon capture

Carbon capture and desulfurization of flue gases are crucial for the achievement of carbon neutrality and sustainable development. In this work, the “one-step” adsorption technology with high-performance metal–organic frameworks (MOFs) was proposed to simultaneously capture the SO2 and CO2. Four machine learning algorithms were used to predict the performance indicators (NCO2+SO2, SCO2+SO2/N2, and TSN) of MOFs, with Multi-Layer Perceptron Regression (MLPR) showing better performance (R2 = 0.93). To address sparse data of MOF chemical descriptors, we introduced the Deep Factorization Machines (DeepFM) model, outperforming MLPR with a higher R2 of 0.95. Then, sensitivity analysis was employed to find that the adsorption heat and porosity were the key factors for SO2 and CO2 capture performance of MOF, while the influence of open alkali metal sites also stood out. Furthermore, we established a kinetic model to batch simulate the breakthrough curves of TOP 1000 MOFs to investigate their dynamic adsorption separation performance for SO2/CO2/N2. The TOP 20 MOFs screened by the dynamic performance highly overlap with those screened by the static performance, with 76 % containing open alkali metal sites. This integrated approach of computational screening, machine learning, and dynamic analysis significantly advances the development of efficient MOF adsorbents for flue gas treatment.

The kinematics of amblypygid (Arachnida) pedipalps during predation: extreme elongation in raptorial appendages does not result in a proportionate increase in reach and closing speed.

The link between form and function is key to understanding the evolution of unique and/or extreme morphologies. Amblypygids, or whip spiders, are arachnids that often have highly elongated spined pedipalps. These limbs are used to strike at, and secure, prey before processing by the chelicerae. Amblypygi pedipalps are multifunctional, however, being used in courtship and contest, and vary greatly in form between species. Increased pedipalp length may improve performance during prey capture, but length could also be influenced by factors including territorial contest and sexual selection. Here, for the first time, we used high-speed videography and manual tracking to investigate kinematic differences in prey capture between amblypygid species. Across six morphologically diverse species, spanning four genera and two families, we created a total dataset of 86 trials (9-20 per species). Prey capture kinematics varied considerably between species, with differences being expressed in pedipalp joint angle ranges. In particular, maximum reach ratio did not remain constant with total pedipalp length, as geometric scaling would predict, but decreased with longer pedipalps. This suggests that taxa with the most elongated pedipalps do not deploy their potential length advantage to proportionally increase reach. Therefore, a simple mechanical explanation of increased reach does not sufficiently explain pedipalp elongation. We propose other factors to help explain this phenomenon, such as social interactions or sexual selection, which would produce an evolutionary trade-off in pedipalp length between prey capture performance and other behavioural and/or anatomical pressures.

Photoinduced enhanced CO2 capture performance on carbon-doped boron nitride adsorbent

The key issues in the CO2 capture industry are the high energy and cost consumption during the capture and regeneration process. Enhancing CO2 adsorption and rapid desorption through switches sunlight irradiation is a promising route. In this study, a series of carbon-doped boron nitride (BCN) adsorbents with different contents were synthesized. The BCN presented a growing CO2 adsorption capacity under light irradiation, implying that sunlight may become a key driving force for the low-cost CO2 capture. During the experiments, the best performing sample BCN(1:3) showed 32 % and 28 % increase in CO2 adsorption capacity after UV light irradiation at 0.15 and 1 bar CO2 pressure, respectively. To explain this interesting phenomenon, a series of tests and analyses had been conducted, such as EPR, Hall effect test and DFT computation. The results confirmed that the enhanced CO2 absorption characteristics can be attributed to the photoelectric effects of generating more free electrons, which enhanced Lewis alkalinity of BCN adsorbents and thus improved their CO2 adsorption capacities. This work, for the first time, utilizes the photoelectric effect to increase the efficient capture capacity of CO2, opening up a new path for the design and research of CO2 capture materials.

The Success-Score in Professional Football: a metric of playing style or a metric of match outcome?

Abstract In the growing field of data analysis in soccer tracking data is analyzed utilizing increasingly complex methods to account for the dynamic, multifactorial nature of the game. One promising approach is the Success-Score combining ball control and space control. The resulting metric is hypothesized to indicate performance levels and to distinguish performance from playing style. Position datasets from one season of the German Bundesliga were analyzed by calculating Success-Scores based on different interval lengths for two different areas. The relative goalscoring frequency above resp. below the 80th percentile and the rank order correlation between goals and Success-Scores was used to assess the relevance of the Success- Score for goalscoring. The influence of the Success-Score on match outcome, accounting for possession and opponent quality was analyzed via mixed linear models. Results indicated a relation between goalscoring and the Success-Scores, as well as a considerable influence of the Success-Scores on match outcome. The mixed linear models allowed to conclude that Success-Scores capture performance rather than just playing style. The results highlight the potential of the general concept of the Success-Score, combining space and ball control. However, the practical value of the Success-Score in its current implementation appears limited and requires further development.

Synthesizing covalent organic frameworks for unprecedented iodine capture performance

Nuclear energy continues to be an important supplier of electricity, but it has problems with waste management and the possibility to leak radioactive material. Iodine, a potentially harmful byproduct of uranium fission, is hazardous to both the environment and human health. Therefore, developing safe, effective, and affordable storage facilities for iodine waste is crucial. Owing to their well-controlled pore structure and substantial certain surface area, covalent organic frameworks (COFs) show promise for the adsorption of radioactive iodine. The newly developed COFs (SJ-COF, YA-COF, and AA-COF) shown amazing properties, including strong thermal and chemical stability, which made them ideal for efficient iodine capture. Notably, the ultrahigh iodine capture capacities of these COFs—8.52 g g−1, 8.12 g g−1 and 7.01 g g−1—were significantly greater than most previously reported materials. And The % removal efficiency for SJ-COF, YA-COF and AA-COF from I2/cyclohexane solutions were 87.9 %, 88.6% and 82.6 % respectively. It is noteworthy that the three COFs have high selectivity, reusability, and iodine retention abilities, maintaining iodine even after five recyclings. Based on the outcomes of the experiments, the adsorption processes of the three COFs were examined, and it was discovered that iodine was bound through physical-chemical adsorption. The findings of our work provide a ground-breaking standard for the removal of nuclear waste and demonstrate the enormous potential of COFs as adaptable porous structures that may be specifically designed to address major environmental concerns.