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Adsorbents‐based gas separation technologies are regarded as the potential energy‐efficient alternatives towards current thermal‐driven methods, and the study on multi‐component gas separation is essential to deepen our understanding of the adsorbents for practical use. Relative to the ideal two‐component mixtures, both the adsorption behavior and separation mechanisms are obviously more complex in multiple gas mixtures due to their close or even overlapped sizes and properties. The emergence of metal–organic frameworks with controllable pore size and pore chemistry provides the platform for the tailor‐made pore structure to satisfy the harsh requirements of multi‐component gas separation. This minireview highlights the recent advance of multi‐component gas separation using metal–organic frameworks, including multiple impurities removal and selective molecular capture. Combining with the typical cases of hydrocarbon separations (C2, C4, and C8), the detailed discussion about the developed strategies (e.g. self‐adaptive binding sites, multiple binding spaces, synergistic binding sites, synergistic sorbent separation technology, gate‐opening effect, size and thermodynamic combine effect) that are adaptive to different scenarios would be provided. The review will conclude with our perspective on the existing barriers and the future direction of this topic. [ABSTRACT FROM AUTHOR]

Aqueous zinc‐ion batteries compatible with a wide temperature range and long cycle lifespan show great application prospects but are greatly limited by the unstable electrode‐electrolyte interfaces and mismatched electrolytes. This report presents the pathway of succinamic acid (SA) additive‐induced built‐in trimodal molecular interaction for constructing sustainable aqueous zinc batteries. As confirmed, such trimodal molecular interaction falls into the following patterns: the binding state of the H─F bond between SA and polyvinylidene fluoride (PVDF) binder, the micellar aggregation state in aqueous electrolyte, and the spontaneous adsorption state at Zn anode–electrolyte interface. Benefiting from the above synergistic effect, the Zn electrode shows a highly reversible deposition/stripping behavior over the wide temperature range (−10–50 °C) when paired with the optimized electrolyte. Specially, an impressive 3530 h‐cycle lifespan of the Zn symmetrical cell is achieved at the conditions of 1 mA cm−2 and 1 mAh cm−2. Beyond that, significantly improved storage capability and cycle performance are demonstrated in both aqueous Zn‐MnO2 and Zn‐I2 batteries. Given the good balance between the working temperature range, ionic conductivity, and Zn2+ transfer number of this trace molecule‐mediated electrolyte, this design paradigm provides new insights into developing advanced aqueous batteries, including but not limited to zinc‐based systems. [ABSTRACT FROM AUTHOR]

Developing artificial protective layers is an effective strategy to address the issue of dendrites for aqueous Zn‐metal batteries (ZMBS). However, drawbacks such as rough microscopic morphology, excessive thickness, and single functionality remain, limiting the attainment of a stable zinc anode. Herein, a novel multifunctional organic–inorganic hybrid artificial protective layer is produced by splicing inorganic fragments onto organic materials in situ using a chemical sewing. The protective layer is well‐compatible and also retains the function of organic and inorganic materials, which not only inhibits dendrite production but also alleviates Zn corrosion. The Si─OH bond of the zincophilic group enables planar Zn deposition while forming hydrogen bonds with water, suppressing water activity near the anode and reducing the hydrogen evolution reaction. As expected, the Zn||Zn symmetric cell with a protective layer provides high cycling stability of more than 1960 h at 1 mA cm−2, which is about 28 times higher than that of the symmetric cell assembled without the protective layer. More importantly, a Zn||V2O5 full cell with an ultra‐long lifetime has been achieved with an artificial protective layer. This work provides a potential viable path to achieve long‐lived ZMBS. [ABSTRACT FROM AUTHOR]

To improve agricultural production efficiency, increase farmers' income, and promote sustainable development, we established a multi-objective optimisation model for crop planting structure in an irrigation area using the grey wolf optimisation (GWO) algorithm to comprehensively consider the resource, economic, and social objectives associated with agriculture. This model was subsequently applied to obtain the optimal planting structure in the southern bank of the Xiaolangdi Reservoir irrigation area in Henan Province, China. The planting areas of wheat, corn, autumn miscellaneous, and economic crops are 30,417; 25,050; 7157; and 1789 hm2, respectively. The irrigation water is 8292.66 × 104 m3, output value of crops is 105,721.37 × 104 CNY, and crop yield is 34,280.31 × 104 kg. Different solutions are used to solve the model to evaluate the results, and the order degree entropy method is used to evaluate and compare the results of multiple solutions. The optimisation scheme obtained with this model is consistent with the evaluation results of the cooperative game optimisation scheme, and the relative order degree entropy is 0.136, which is better than that in other schemes. Thus, the optimisation scheme of crop planting structure obtained via GWO comprehensively considers irrigation water consumption, economic benefits, and crop yield, which ensures coordinated development of resource, economic, and social systems and is conducive to promoting the benign development of the whole irrigation area system. [ABSTRACT FROM AUTHOR]

The high electronic conductivity and tailorable structural properties of MXene materials make them promising candidates for energy storage. However, their poor chemical instability and self‐stacking effect greatly limit their application, especially in aqueous systems. Here, using a eutectic etching approach, hydroxylated borophene is used as a trifunctional mediator to construct robust Ti3C2Tx‐based MXene/B self‐assembled film electrodes for zinc‐ion capacitors (ZICs). Due to this mediator, the as‐formed strong interfacial binding within the heterostructure can give rise to an integrated modification effect and promote high‐efficiency interface energy storage. One is to strengthen the thermodynamic stability of local Ti─O bonds and inhibit the irreversible degradation of MXene; two is to enlarge the interface space of the MXene electrode and boost the ion transport; three is to improve the interfacial Zn2+ trapping ability without affecting Zn2+ migration on the MXene surface. Thus, the MXene/B electrode exhibits a high areal capacitance (537.9 mF cm−2) at a current density of 0.2 mA cm−2 and an extraordinary cycling stability at 1 mA cm−2, with 99.64% retention after 40 000 cycles, which far surpasses that of most previous reports. This work provides a pathway for overcoming the interface storage limit of MXene electrodes to construct high‐performance ZICs. [ABSTRACT FROM AUTHOR]

Aqueous zinc‐ion batteries (AZIBs) hold great potential for grid‐scale energy storage systems, owing to their intrinsic safety and low cost. Nevertheless, their industrialization faces challenges of severe Zn dendrites and parasitic reactions. In this study, sulfonated cellulose separator (denoted as CF‐SO3) with low thickness, exceptional mechanical strength, and large ionic conductivity is developed. Benefiting from the electrostatic repulsion between ─SO3− functional groups and SO42− anions and the strongly interaction between ─SO3− and Zn2+ cations, the migration of SO42− anions can be restricted, the 2D diffusion of Zn2+ ions at the surface of Zn electrode can be suppressed, and the desolvation of hydrated Zn2+ ions can be promoted. Concurrently, the homogeneous nanochannels within CF‐SO3 separator can ensure uniform electric field and Zn2+ ion flux. With these benefits, the CF‐SO3 separator enables Zn//Zn cells to run stably for 1200 h at 4 mAh cm−2 by facilitating oriented and dendrite‐free Zn deposition. Under a large depth of discharge of 68.3%, a life span of 400 h can still be achieved. Additionally, the reliability of CF‐SO3 separator is confirmed in Zn//MnO2 and Zn//H11Al2V6O23.2 full batteries with high mass loading conditions. This work provides valuable guidance for the advancement of high‐performance separators of AZIBs. [ABSTRACT FROM AUTHOR]

Here, lithium ions inserted crystalline carbon nitrides (LCCN) with different defect concentrations are prepared by elaborately regulating the mass transfer process in thermal polymerization. It is revealed that there is no conventional exciton–polarons‐induced exciton dissociation mechanism in LCCN due to the weak coupling between excitons and phonons. On the contrary, excitons continue to trap/detrap through defect‐induced traps, which weakens the Coulomb force between electron–hole pairs, thereby accelerating exciton dissociation. It is worth emphasizing that this is the first systematic research on the exciton dissociation characteristics and photocatalytic activity of LCCN of poly(heptazine imide) structure. A strategy of assisting exciton dissociation through defect‐induced traps to address the inherently high exciton binding energy and low exciton dissociation efficiency issues in polymer photocatalysts is proposed. [ABSTRACT FROM AUTHOR]

Aqueous zinc‐ion batteries (AZIBs) suffer from rampant Zn dendrites growth, corrosion and sluggish transport kinetics, all of which have a serious impact on their performance and practical applications. Therefore, porous carbon nanofibers (BTO@PCNFs) loaded with BaTiO3 nanoparticles (BTO NPs) are constructed as a multifunctional interlayer for stabilizing the Zn anodes. Owing to the synergistic effect of BTO NPs and 3D porous carbon framework, this interlayer can achieve uniform electric field distribution, accelerate Zn2+ migration, and promote ion flux homogenization, thus leading to uniform Zn deposition. Meanwhile, the BTO@PCNFs interlayer demonstrates excellent anti‐corrosion effect, which can effectively prevent the side reactions. Benefiting from the synergistic effect of interlayers, the BTO@PCNFs multifunctional interlayers achieve a comprehensive optimization of the Zn anodes. The BTO@PCNFs‐Zn electrode exhibits lower nucleation overpotential (33.5 mV) at 0.5 mA cm−2. The Zn//Zn symmetrical cell with BTO@PCNFs interlayer exhibits ultra‐low overpotential (14 mV) and ultra‐long cycle life (5250 h at 0.5 mA cm−2). Even at high current density (30 mA cm−2), the BTO@PCNFs‐Zn electrode can be stably cycled for more than 830 h, achieving an ultra‐high cumulative capacity of 12 450 mAh cm−2. The multifunctional interlayers can provide a reference for the design of high‐performance Zn anodes. [ABSTRACT FROM AUTHOR]

Statistics has played an increasingly important role in applied linguistics research. However, little research has been available that sheds light on statistical literacy among early‐career researchers of applied linguistics. The study reported in this article surveyed statistical literacy, attitudes toward statistics, and statistics self‐efficacy among Chinese applied linguistics research students and further examined the inter‐variable relationships. Based on analyses of the cross‐sectional survey of 211 master's students, we found that: (1) the students' overall statistical literacy was not satisfying; (2) although they thought positively of statistics, they were not particularly confident with statistics; (3) the three experience‐related variables—the number of statistics courses taken, quantitative research orientation, and self‐training—were important predictors of statistical literacy, attitudes toward statistics, and statistics self‐efficacy; and (4) statistics self‐efficacy seemed to mediate the relationship between attitudes toward statistics and statistical literacy. We discussed these findings in relation to improving statistics courses in applied linguistics program in China and to statistics learning and teaching. [ABSTRACT FROM AUTHOR]

One‐step separation of C2H4 from ternary gas mixtures containing acetylene (C2H2), ethylene (C2H4), and carbon dioxide (CO2) represents a great challenge in chemical industry. Herein, we report the electro‐field alignment in a novel anion‐pillared MOF (SIFSIX‐TEPE‐Cu) for benchmark C2H4 separation from C2H2/CO2/C2H4 gas mixtures. The semi‐cage cavities featuring capped facets generated negative potentials along anion pillars and compensatory positive‐charged electro‐fields along organic ligands (TEPE) that facilitate specific recognitions of C2H2 and CO2 over C2H4. As a result, SIFSIX‐TEPE‐Cu exhibits high adsorption capacities for C2H2 (123 cm3 g−1) and CO2 (65 cm3 g−1) at 1.0 bar and 298 K. Notably, the record‐high C2H2 uptake (78 cm3 g−1) at 0.01 bar and remarkable C2H2/C2H4 selectivity (615.2) renders benchmark trace C2H2 removal ability. Dynamic breakthrough experiments demonstrate the benchmark productivity for high‐purity C2H4 (>99.995%) of 194.7 mol kg−1 and 5.96 mol kg−1 from binary C2H2/C2H4 (1/99, v/v) and ternary C2H2/CO2/C2H4 (1/9/90, v/v/v) gas mixtures. [ABSTRACT FROM AUTHOR]

Borate-phosphates exhibit a wide range of compositional and structural diversity, making them ideal hosts for luminescent materials. In this work, a new borate-phosphate compound CsNa2Dy2(BO3)(PO4)2 has been prepared under high temperature solution growth method. It crystallizes in an orthorhombic space group Cmcm with the following lattice parameters determined by single-crystal X-ray diffraction: a = 6.9709(5), b = 14.9699(11), c = 10.6480(8) Å, z = 4. Its structure contains isolated BO3 planar triangles and PO4 tetrahedra, which are interconnected by Cs+, Na+ and Dy3+ ions. Solid solutions of CsNa2Y2(1−x)Dy2x(BO3)(PO4)2 (x = 0 − 0.08) are prepared and exhibit a yellow emissive luminescence by near-UV excitation due to the 4F9/2 → 6H(13/2, 15/2) transitions of Dy3+. The optimized concentration of Dy3+ is x = 0.01, and if over this critical value, the luminescent intensity will decrease due to concentration quenching. The Commission International de L'Eclairage (CIE) coordinates for CsNa2Y1.98Dy0.02(BO3)(PO4)2 are (x = 0.377, y = 0.404), corresponding to yellow color. The prepared phosphor may serve as a yellow phosphor for NUV-excited LEDs. [ABSTRACT FROM AUTHOR]

Multiple impurities removal represents one of the most daunting challenges in gas purification, but the attainment of efficient adsorptive separation is hindered by the difficulty in designing adsorbents that could simultaneously capture different impurities. Herein, we revealed a molecular trap within Zn‐trz‐ox (trz = 1,2,4‐triazole; ox = oxalic acid) that featured positive H and negative O sites, and the suitable pore size, which exhibited remarkable one‐step C2H4 purification performance directly from quaternary C2H4/C2H2/C2H6/CO2 mixtures. The separation selectivities of C2H4 with respect to CO2, C2H2, and C2H6 are 9.8, 2.6, and 2.5, higher than the sole adsorbent yet reported. Meanwhile, polymer grade C2H4 (≥99.95%) could be directly obtained with record C2H4 productivity of 1.5 mol kg−1, over 10 times higher than that of the previous benchmark material. The deep insight into the binding behavior revealed by simulation studies offers important clues for the design of advanced adsorbent for multiple impurities capture. [ABSTRACT FROM AUTHOR]

Frequent wildfires associated with emplacement of the Central Atlantic Magmatic Province (CAMP) are thought to have been important drivers of two significant changes in terrestrial plant communities and diversity during the Triassic-Jurassic Mass Extinction (TJME, ca. 201.51 Ma). However, it remains to be investigated whether these two changes are potentially related to different wildfire types. To better understand this relationship, we used a new method to reanalyze fossil pollen and spores across the Triassic-Jurassic transition in the Jiyuan Basin from the North China Plate. Results show that two peaks in wildfire frequency experienced different types of wildfires, with each linked to significant changes in plant communities and diversity losses. In the first wildfire peak, canopy fires dominated and are accompanied by significant losses of canopy forming plants, while in the second wildfire peak, ground cover fires dominated accompanied by significant losses of ground cover plants. Changes in atmospheric humidity conditions were an important control on the two different wildfire peaks. Relatively humid climatic conditions corresponded to the prevalence of canopy fires and hindered the spread and development of ground cover fires in wet surface conditions. Conversely, relatively arid climatic conditions corresponded with the prevalence of ground cover fires in dry surface environments. Our results provide a potential relationship between terrestrial plant communities and wildfire types, which is important to further understanding of terrestrial environmental and floral changes driven by Large Igneous Provinces. [ABSTRACT FROM AUTHOR]

Olefin/paraffin separations are among the most energy-intensive processes in the petrochemical industry, with ethylene being the most widely consumed chemical feedstock. Adsorptive separation utilizing molecular sieving adsorbents can optimize energy efficiency, whereas the size-exclusive mechanism alone cannot achieve multiple olefin/paraffin sieving in a single adsorbent. Herein, an unprecedented sieving adsorbent, BFFOUR-Cu-dpds (BFFOUR = BF4-, dpds = 4,4'-bipyridinedisulfide), is reported for simultaneous sieving of C2-C4 olefins from their corresponding paraffins. The interlayer spaces can be selectively opened through stronger guest-host interactions induced by unsaturated C = C bonds in olefins, as opposed to saturated paraffins. In equimolar six-component breakthrough experiments (C2H4/C2H6/C3H6/C3H8/n-C4H8/n-C4H10), BFFOUR-Cu-dpds can simultaneously divide olefins from paraffins in the first column, while high-purity ethylene (> 99.99%) can be directly obtained through the subsequent column using granular porous carbons. Moreover, gas-loaded single-crystal analysis, in-situ infrared spectroscopy measurements, and computational simulations demonstrate the accommodation patterns, interaction bonds, and energy pathways for olefin/paraffin separations. Olefin/paraffin separations are challenging in chemical industry. Here, authors report a sieving adsorbent for separating C2-C4 olefins from counterpart paraffins. The interlayer spaces are selectively opened via stronger guest-host interactions induced by olefins, as opposed to saturated paraffins. [ABSTRACT FROM AUTHOR]

The sluggish ion transport kinetics and poor interface compatibility are the major challenges for developing high‐performance solid‐state zinc metal batteries. Here, using the densified polyacrylonitrile/silicon dioxide (PAN‐SiO2) nanofiber membrane as a unique multifunctional mediator, a novel mediator‐bridged type of ultrathin (28.6 µm) polymer electrolyte that is rationally designed. The PAN/SiO2 /polyethylene oxide/Zn(OTf)2(PSPZ) polymer electrolyte is demonstrated to significantly enhance multiple kinetics. In addition to superior mechanical properties, the efficient thermal conductive effect endows it with good high‐temperature structural stability. Interestingly, a unique PAN skeleton‐locking‐anion‐enabled fast ion transport mechanism is uncovered to achieve a high Zn2+ migration number (0.71). Moreover, an efficient dendrite‐free Zn deposition guided by a flat dense SEI is demonstrated. In this case, highly reversible Zn metal anodes can be realized in the temperature range extending to −25–80 °C, as well as an impressive 4800 h‐cycle lifespan at the condition of 0.1 mA cm−2. Beyond that, wide‐temperature, high‐rate, durable PSPZ‐based solid‐state Zn/VO2 batteries are also successfully verified. This brand‐new concept of multiple‐kinetics‐enhanced polymer electrolyte design can provide a new perspective for developing all‐climate fast‐charging solid‐state batteries, including but not limited to zinc metal batteries. [ABSTRACT FROM AUTHOR]

The development of high energy/power density and long lifespan device is always the frontier direction and attracts great research attention in the energy storage fields. Zinc‐ion capacitors (ZICs), as an integration of zinc‐ion batteries and supercapacitors, have been widely regarded as one of the viable future options for energy storage, owing to their variable system assembly method and potential performance improvement. However, the research of ZICs still locate at initial stage until now, and how to construct the suitable systems for different condition is still challenging. Herein, the recent advance in the rational design of ZICs is reviewed in order to construct related theory including compatible principle and design paradigm. It starts with a systematically summary of the fundamental theory as well as the motivation. Then, the electrode materials are classified into capacitor‐type and battery‐type based on the storage mechanism, and the design strategies and progress of these two‐type candidates are comprehensively discussed, aiming to reveal the inherent relationship between the performance of devices and the component as well as architecture of electrode materials. Beyond that, the future perspectives in this emerging field are also given, expecting to guide the construction of high‐performance ZICs for practical applications and boost its development. [ABSTRACT FROM AUTHOR]

The zinc (Zn) anode in zinc‐ion batteries suffers from potential defects such as wild dendrite growth, severe Zn corrosion, and violent hydrogen evolution reaction, inducing erratic interfacial charge transfer kinetics, which eventually leads to electrochemical failure. Here, collagen, a biomacromolecule, is added to achieve the reconstruction of the electrolyte hydrogen‐bonding network and the modification of the derived Zn interface. Benefiting from the electronegativity advantage of amino groups (‐NH2) in collagen, the Zn (002) crystal plane is preferentially exposed and the solid electrolyte interface (SEI) rich in ZnF2 and Zn3N2 promotes the rapid charge transfer of Zn anode. Thence, an impressive cumulative capacity of 7,500 mAh cm−2 at 30 mA cm−2 is achieved and the assembled Zn|VO2 cell exhibited robust cycle reversibility even when subject to a maximum current of 100 A g−1 and an ultra‐long cycle life of 20,000 cycles at 50 A g−1, with a single‐cycle capacity loss as low as 0.0021%. Such a convenient strategy of solvent sheathing regulation and derived interfacial manipulation opening up a promising universal approach toward long‐life and high‐rate Zn anodes. [ABSTRACT FROM AUTHOR]

The design of electrode compatible with wide‐temperature, fast‐charging, and long‐lifespan aqueous zinc‐ion batteries is a great challenge that urgently needs addressing. However, the mismatch between runaway host dissolution and high interfacial hydrophilicity within electrode is a contradictory problem that restricts their electrochemical performance. In this report, take the typical vanadium diselendie (VSe2) host for example, by employing the natural polymer bacterial cellulose (BC) as the multifunctional mediator, a design paradigm of self‐assembly hybrid electrode with efficient tandem electrochemistry is presented. Theoretical and experimental research confirmed that such BC‐mediated hybrid structure exhibits multiple functions to well balance the cathode dissolution and storage kinetics. Impressively, such an electrode displayed an excellent rate capability (1–50 A g−1), and an unexpected record‐lifespan of 45 000 cycles. Beyond that, it also shows a good temperature‐tolerance ability, remaining the high specific capacities of 120 and 288 mAh g−1 (at 10 A g−1) after 3000 cycles at −25 and 50 °C, respectively. Note that such approach is also applicable to the high‐voltage platform MnO2 and I2 hosts, demonstrating its potential for universality. This discovery can provide a new design principle of robust electrode for advanced aqueous zinc‐ion batteries. [ABSTRACT FROM AUTHOR]

Borate-phosphates exhibit a wide range of compositional and structural diversity, making them ideal hosts for luminescent materials. In this work, a new borate-phosphate compound CsNa2Dy2(BO3)(PO4)2 has been prepared under high temperature solution growth method. It crystallizes in an orthorhombic space group Cmcm with the following lattice parameters determined by single-crystal X-ray diffraction: a = 6.9709(5), b = 14.9699(11), c = 10.6480(8) Å, z = 4. Its structure contains isolated BO3 planar triangles and PO4 tetrahedra, which are interconnected by Cs+, Na+ and Dy3+ ions. Solid solutions of CsNa2Y2(1−x)Dy2x(BO3)(PO4)2 (x = 0 − 0.08) are prepared and exhibit a yellow emissive luminescence by near-UV excitation due to the 4F9/2 → 6H(13/2, 15/2) transitions of Dy3+. The optimized concentration of Dy3+ is x = 0.01, and if over this critical value, the luminescent intensity will decrease due to concentration quenching. The Commission International de L'Eclairage (CIE) coordinates for CsNa2Y1.98Dy0.02(BO3)(PO4)2 are (x = 0.377, y = 0.404), corresponding to yellow color. The prepared phosphor may serve as a yellow phosphor for NUV-excited LEDs. [ABSTRACT FROM AUTHOR]

Background: APRI and FIB-4 scores are used to exclude clinically significant fibrosis (defined as stage ≥ F2) in patients with chronic viral hepatitis. However, the cut-offs for these scores (generated by Youden indices) vary between different patient cohorts. This study aimed to evaluate whether serum dithiothreitol-oxidizing capacity (DOC), i.e., a surrogate test of quiescin sulfhydryl oxidase-1, which is a matrix remodeling enzyme, could be used to non-invasively identify significant fibrosis in patients with various chronic liver diseases (CLDs)., Methods: Diagnostic performance of DOC was compared with APRI and FIB-4 for identifying significant fibrosis. ROC curve analyses were undertaken in: a) two chronic hepatitis B (CHB) cohorts, independently established from hospitals in Wenzhou (n = 208) and Hefei (n = 120); b) a MASLD cohort from Wenzhou hospital (n = 122); and c) a cohort with multiple CLD etiologies (except CHB and MASLD; n = 102), which was identified from patients in both hospitals. Cut-offs were calculated using the Youden index. All CLD patients (n = 552) were then stratified by age for ROC curve analyses and cut-off calculations., Results: Stratified by CLD etiology or age, ROC curve analyses consistently showed that the DOC test was superior to APRI and FIB-4 for discriminating between clinically significant fibrosis and no fibrosis, when APRI and FIB-4 showed poor/modest diagnostic performance (P < 0.05, P < 0.01 and P < 0.001 in 3, 1 and 3 cohort comparisons, respectively). Conversely, the DOC test was equivalent to APRI and FIB-4 when all tests showed moderate/adequate diagnostic performances (P > 0.05 in 11 cohort comparisons). DOC had a significant advantage over APRI or FIB-4 scores for establishing a uniform cut-off independently of age and CLD etiology (coefficients of variation of DOC, APRI and FIB-4 cut-offs were 1.7%, 22.9% and 47.6% in cohorts stratified by CLD etiology, 2.0%, 26.7% and 29.5% in cohorts stratified by age, respectively). The uniform cut-off was 2.13, yielded from all patients examined. Surprisingly, the uniform cut-off was the same as the DOC upper limit of normal with a specificity of 99%, estimated from 275 healthy control individuals. Hence, the uniform cut-off should possess a high negative predictive value for excluding significant fibrosis in primary care settings. A high DOC cut-off with 97.5% specificity could be used for detecting significant fibrosis (≥ F2) with an acceptable positive predictive value (87.1%)., Conclusions: This proof-of-concept study suggests that the DOC test may efficiently rule out and rule in significant liver fibrosis, thereby reducing the numbers of unnecessary liver biopsies. Moreover, the DOC test may be helpful for clinicians to exclude significant liver fibrosis in the general population., (© 2024. The Author(s).)

Olefin/paraffin separations are among the most energy-intensive processes in the petrochemical industry, with ethylene being the most widely consumed chemical feedstock. Adsorptive separation utilizing molecular sieving adsorbents can optimize energy efficiency, whereas the size-exclusive mechanism alone cannot achieve multiple olefin/paraffin sieving in a single adsorbent. Herein, an unprecedented sieving adsorbent, BFFOUR-Cu-dpds (BFFOUR = BF 4 - , dpds = 4,4'-bipyridinedisulfide), is reported for simultaneous sieving of C 2 -C 4 olefins from their corresponding paraffins. The interlayer spaces can be selectively opened through stronger guest-host interactions induced by unsaturated C = C bonds in olefins, as opposed to saturated paraffins. In equimolar six-component breakthrough experiments (C 2 H 4 /C 2 H 6 /C 3 H 6 /C 3 H 8 /n-C 4 H 8 /n-C 4 H 10 ), BFFOUR-Cu-dpds can simultaneously divide olefins from paraffins in the first column, while high-purity ethylene ( > 99.99%) can be directly obtained through the subsequent column using granular porous carbons. Moreover, gas-loaded single-crystal analysis, in-situ infrared spectroscopy measurements, and computational simulations demonstrate the accommodation patterns, interaction bonds, and energy pathways for olefin/paraffin separations., (© 2024. The Author(s).)