Open Reduction and Internal Fixation for Supination-External Rotation Type IV Ankle Fractures by Means of Anterolateral and Posterolateral Approaches.

BACKGROUND: The present study aimed to analyze and compare the efficacy of the anterolateral and posterolateral approaches for surgical treatment of supination-external rotation type IV ankle fractures. METHODS: This retrospective study enrolled 60 patients (60 feet) with supination-external rotation type IV ankle fractures, including 30 patients (30 feet) treated by means of the anterolateral approach and 30 patients (30 feet) treated by means of the posterolateral approach. Postoperative clinical efficacy was compared between the groups based on operation time, intraoperative blood loss, postoperative complications, fracture healing time, visual analog scale scores, Short Form-36 Health Survey scores, and American Orthopedic Foot and Ankle Society scores. Comparisons between the two groups were performed using independent-samples t tests and analyses of variance. Intragroup differences were compared using paired t tests, and the χ2 test was used to compare categorical variables. RESULTS: All 60 included patients completed follow-up ranging from 12 to 18 months (mean duration, 14.8 ± 3.5 months). Although baseline characteristics were similar in the two groups, there were significant differences in operation time (86.73 ± 17.44 min versus 111.23 ± 10.05 min; P < .001) and intraoperative blood loss (112.60 ± 25.05 mL versus 149.47 ± 44.30 mL; P < .001). Although fracture healing time (10.90 ± 0.66 weeks versus 11.27 ± 0.94 weeks; P = .087) was shorter in the anterolateral group than in the posterolateral group, the difference was not significant. Postoperative complications occurred in one and three patients in the anterolateral and posterolateral approach groups, respectively. Visual analog scale scores were significantly lower in the anterolateral group than in the posterolateral group (1.43 ± 0.50 versus 1.83 ± 0.75; P = .019), although there was no significant difference in Short Form-36 Health Survey scores between the groups (73.63 ± 4.07 versus 72.70 ± 4.04; P = .377). However, American Orthopedic Foot and Ankle Society scores were higher in the anterolateral group than in the posterolateral group (80.43 ± 4.32 versus 75.43 ± 11.32; P = .030). CONCLUSIONS: Both the anterolateral and posterolateral approaches can achieve good results in the treatment of supination-external rotation type IV ankle fractures. Compared with the posterolateral approach, the anterolateral approach is advantageous for the treatment of supination-external rotation type IV ankle fractures given its safety and ability to reduce trauma, clear field of view revealed, and allow for exploration and repair of the inferior tibiofibular anterior syndesmosis within the same incision.

Rapid recovery of high pure PbO from spent lead acid battery without desulfation and chemicals consumption method.

The direct recovery of high-purity PbO from spent lead paste without a pre-desulfation process has significant industrial promise. Herein, we propose a recyclable, ultra-fast, and high value-added closed-loop of high-purity PbO recovery process by intensive multidentate coordination of histidine with crude 2PbO·PbSO4 by a rotating liquid-film (RLF) reactor and CO2 carbonation-dissociation. Parameter optimizations and kinetic calculations show the leaching time is shortened from 40 min to 60 s with 99.14 % leaching rate and 99.99 % PbO purity by internal diffusion control, where the RLF reactor promotes mass transfer and reaction rates by instantly renewing the surface of crude 2PbO·PbSO4. Furthermore, all 5 batches reveal that the separation of SO42- ions from the regenerated mother liquid with Ba(OH)2 significantly improves the recycling rate of the mother liquid and high-purity PbO product. This new strategy reveals a bright prospect of a highly efficient, high value-added, and environmentally friendly recycling route for solid waste resources.

Precise Tuning of Hollow and Pore Size of Bimetallic MOFs Derivate to Construct High-Performance Nanoscale Materials for Supercapacitors and Sodium-Ion Batteries.

Precise control of pore volume and size of carbon nanoscale materials is crucial for achieving high capacity and rate performances of charge/discharge. In this paper, starting from the unique mechanism of the role of In, Zn combination, and carboxyl functional groups in the formation of the lumen and pore size, the composition of InZn-MIL-68 is regulated to precisely tune the diameter and wall pore size of the hollow carbon tubes. The hollow carbon nanotubes (CNT) with high-capacity storage and fast exchange of Na+ ions and charges are prepared. The CNT possess ultra-high specific capacitance and ultra-long cycle life and also offer several times higher Na+ ion storage capacity and rate performance than the existing CNTs. Density functional theory calculations and tests reveal that these superior characteristics are attributed to the spacious hollow structure, which provides sufficient space for Na+ storage and the tube wall's distinctive porosity of tube wall as well as open ends for facilitating Na+ rapid desorption. It is believed that precise control of sub-nanopore volume and pore size by tuning the composition of the carbon materials derived from bimetallic metal-organic frameworks (MOFs) will establish the basis for the future development of high-energy density and high-power density supercapacitors and batteries.

Bimetallic-MOF Derived Carbon with Single Pt Anchored C4 Atomic Group Constructing Super Fuel Cell with Ultrahigh Power Density And Self-Change Ability.

Pursuing high power density with low platinum catalysts loading is a huge challenge for developing high-performance fuel cells (FCs). Herein, a new super fuel cell (SFC) is proposed with ultrahigh output power via specific electric double-layer capacitance (EDLC) + oxygen reduction reaction (ORR) parallel discharge, which is achieved using the newly prepared catalyst, single-atomic platinum on bimetallic metal-organic framework (MOF)-derived hollow porous carbon nanorods (PtSA /HPCNR). The PtSA-1.74 /HPCNR-based SFC has a 3.4-time higher transient specific power density and 13.3-time longer discharge time with unique in situ self-charge and energy storage ability than 20% Pt/C-based FCs. X-ray absorption fine structure, aberration-corrected high-angle annular dark-field scanning transmission electron microscope, and density functional theory calculations demonstrate that the synergistic effect of Pt single-atoms anchored on carbon defects significantly boosts its electron transfer, ORR catalytic activity, durability, and rate performance, realizing rapid " ORR+EDLC" parallel discharge mechanism to overcome the sluggish ORR process of traditional FCs. The promising SFC leads to a new pathway to boost the power density of FCs with extra-low Pt loading.

Ultra-Fast Recyclable and Value-Added Desulfation Method for Spent Lead Paste via Dual Intensification Processes.

The new low-cost clean pre-desulfation technology is very important in pyrometallurgy and hydrometallurgy. However, traditional reactors have low space-time yield and desulfation rate, resulting in high energy consumption and SO2 emissions in the industrial desulfation processes. Herein, dual rotating liquid film reactors (RLFRs) and lime are proposed to construct a recyclable, ultra-fast, and value-added desulfation method. Parameter optimization and kinetic calculations prove that the above reactions are controlled by internal diffusion, revealing that RLFR promotes the mass transfer and reaction rate. The new process greatly shortens the desulfation time of lead paste from 40 min to 10 s with a high desulfation rate of 99.7%, and the sulfation time of lime from 30 min to 30 s with a sulfation rate of 98.6% with a net profit of 55.99 ¥/ton by cost accounting. Moreover, ten batches of continuous scale-up experiments demonstrate the stability of processes, the desulfation and sulfation rates are kept at 99.7% and 98.2%, which greatly reduces the emissions of waste desulfate liquor. This work provides a new universal strategy for a sustainable, low-cost, and clean desulfation method of waste resources to achieve technical and economic feasibility.

Long-Term Care Research in the Context of COVID-19 Pandemic: A Bibliometric Analysis.

Despite the increasing awareness of long-term care (LTC) research after the outbreak of COVID-19 pandemic, little attention was given to quantitatively describe the evolution of the research field during this period. A total of 1024 articles retrieved from the Web of Science Core Collection database were systematically analyzed using CiteSpace visualization software. The overall characteristics analysis showed that, in the context of the pandemic, attention to LTC research increased significantly-over 800 articles were published in the past two years. The USA, Canada, Italy, and England formed the leading LTC research group, which was consistent with the conclusions of existing bibliometric studies on LTC research before the outbreak. A rigorous analysis based on a dual perspective of references and keywords was applied to reveal that, compared with previous studies, in the context of the pandemic, the focus shifted from the mental and physical health status of older adults in need of LTC to the impact of the pandemic on those of older adults in LTC facilities, from the prevention of general epidemics to the prevention and response of significant public health emergencies, from providing and paying for LTC to strategies for LTC facilities to improve the quality of LTC and well-being of their residents during the pandemic. These findings can provide help and reference for academics, civil folks, and LTC practitioners, as well as help with the sustainable development of LTC research in the context of COVID-19 pandemic.

Intelligent Chip-Controlled Smart Oxygen Electrodes for Constructing Rechargeable Zinc-Air Batteries with Excellent Energy Efficiency and Durability.

High-performance rechargeable oxygen electrodes are key devices for realizing high-specific-energy batteries, including zinc-air and lithium-air batteries. However, these batteries have severe problems of premature decay in energy efficiency by serious corrosion, wide charge-discharge gap, and catalyst peeling off. Herein, we propose a "smart dual-oxygen electrode", which is composed of an intelligent switch control module + heterostructured Fe1Ni3-LDH/PNCNF OER catalysis electrode layer + ion conductive | electronic insulating membrane + Pt/C ORR catalysis electrode layer, where OER and ORR layers are automatically switched by the intelligent switch control module as required. This smart dual-oxygen electrode offers an ultralow energy efficiency decay rate of 0.0067% after 300 cycles during cycling, much lower than that of the commercial Pt/C electrode (1.82%). The assembled rechargeable zinc-air battery (RZAB) displays a super narrow voltage gap and achieves a high energy efficiency of 71.7%, far higher than that of the existing RZABs (about 50%). Therefore, this strategy provides a complete solution for designing various high-performance metal-air secondary batteries.

In-MOF-Derived Hierarchically Hollow Carbon Nanostraws for Advanced Zinc-Iodine Batteries.

Hollow carbon materials are regarded as crucial support materials in catalysis and electrochemical energy storage on account of their unique porous structure and electrical properties. Herein, an indium-based organic framework of InOF-1 can be thermally carbonized under inert argon to form indium particles through the redox reaction between nanosized indium oxide and carbon matrix. In particular, a type of porous hollow carbon nanostraw (HCNS) is in situ obtained by combining the fusion and removal of indium within the decarboxylation process. The as-synthesized HCNS, which possesses more charge active sites, short and quick electron, and ion transport pathways, has become an excellent carrier for electrochemically active species such as iodine with its unique internal cavity and interconnected porous structure on the tube wall. Furthermore, the assembled zinc-iodine batteries (ZIBs) provide a high capacity of 234.1 mAh g-1 at 1 A g-1 , which ensures that the adsorption and dissolution of iodine species in the electrolyte reach a rapid equilibrium. The rate and cycle performance of the HCNS-based ZIBs are greatly improved, thereby exhibiting an excellent capacity retention rate. It shows a better electrochemical exchange capacity than typical unidirectional carbon nanotubes, making HCNS an ideal cathode material for a new generation of high-performance batteries.

Ni(II)-Mediated Photochemical Oxidative Esterification of Aldehydes with Phenols.

The photopromoted, Ni-catalyzed acceptorless dehydrogenation esterification of phenols and aromatic aldehydes has been achieved in an oxidant- and external photosensitizer-free manner. This reliable and atom-economical transformation was tolerant to a wide range of functional groups and proceeded efficiently to give various aryl benzoates in moderate to high yields. Additionally, this photocatalytic system displayed high activity for the hydrogen-evolution cross coupling of aliphatic aldehydes and phenols employing dual nickel and aromatic aldehyde catalysis.

Ion Motor as a New Universal Strategy for the Boosting the Performance of Zn-Ion Batteries.

The quiescent electrolyte causes serious concentration polarization and dendrite problems during the charging and discharging of the battery, which restricts the development of metal secondary batteries and flow batteries. Herein, we report a new concept of ion motors, with which the directional driving and uniformity of the electrolyte are realized to eliminate the concentration polarization and dendritic phenomenon for secondary metal batteries and flow batteries without additional external energy. In this study, a dendrite-free secondary metal battery with ion motors is constructed to eliminate a considerable concentration polarization voltage by a tiny induced counter electromotive force generated by Lorentz force, significantly improving the output power and energy efficiency of the battery. An actual pump-free flow battery with an ion motor is also assembled, which overcomes the problems of low energy efficiency and the complex structure caused by the traditional flow battery requiring 1-2 pumps to drive the electrolyte. The efficiency of ion motors to drive the electrolyte is hundreds of times higher than that of the mechanical pump. Therefore, the ion motor provides a universal strategy for designing more pump-free flow batteries and metal secondary batteries without the risk of dendrites in the future.

Mapping the Global Landscape of Long-Term Care Insurance Research: A Scientometric Analysis.

With the aging population increasing dramatically and the high cost of long-term care (LTC), long-term care insurance (LTCI) has expanded rapidly across the world. This review aims to summarize the status quo, evolution trends, and new frontiers of global LTCI research between 1984 and 2021 through a comprehensive retrospective analysis. A total of 1568 articles retrieved from the Web of Science Core Collection database were systematically analyzed using CiteSpace visualization software (CiteSpace 5.8. R2, developed by Dr. Chaomei Chen at Drexel University (Philadelphia, PA, USA)). The overall characteristics analysis showed that LTCI is an emerging research field in a rapid development stage-nearly 50% of articles were published in the past five years. The most productive LTCI research institutions and authors are located primarily in Japan and the USA. A rigorous analysis based on a dual perspective of references and keywords was applied to reveal that common LTCI hot topics include disability in the elderly, LTC financing, demand for and supply of LTCI, and LTCI systems. In addition, LTCI research trends have shifted from the supply side to the demand side, and from basic studies to practical applications. The new research frontiers are frailty in the elderly, demand for LTCI, and LTCI systems. These findings can provide help and reference for public health practitioners and researchers, as well as help with the sustainable development of LTCI research.

Couple of Nonpolarized/Polarized Electrodes Building a New Universal Electrochemical Energy Storage System with an Impressive Energy Density.

Herein, we propose a new concept of energy storage system composed of a nonpolarized electrode and a polarized electrode (PPE) with an impressive energy density. It offered nearly 4 times higher energy density than that of carbon-based supercapacitor. Among the suggested potential PPE system, we introduced an electrodeposited nanozinc on the copper foam as the nearly nonpolarized electrode and a Zn-2,5-dihydroxyterephthalic acid (DHTA) metal-organic framework (MOF)-derived activated porous carbon as a nearly polarized electrode in KOH-ZnO electrolyte to constitute the C|Zn PPE system prototype. The C|Zn system achieved an impressive energy density of 84.5 Wh kg-1 at 1000 W kg-1, 4 times higher than that of the C|C supercapacitor. It also shows a high capacitance retention rate of 94.5% at 10 A g-1 after 10 000 cycles. Therefore, the amazing results indicate that the PPE energy system integrates the advantages of supercapacitors and secondary batteries. It will be a promising and effective energy device for higher-performance electric vehicles.

Rational Design and Growth of MOF-on-MOF Heterostructures.

Multiporous metal-organic frameworks (MOFs) have emerged as a subclass of highly crystalline inorganic-organic materials, which are endowed with high surface areas, tunable pores, and fascinating nanostructures. Heterostructured MOF-on-MOF composites are recently becoming a research hotspot in the field of chemistry and materials science, which focus on the assembly of two or more different homogeneous or heterogeneous MOFs with various structures and morphologies. Compared with one single MOF, the dual MOF-on-MOF composites exhibit unprecedented tunability, hierarchical nanostructure, synergistic effect, and enhanced performance. Due to the difference of inorganic metals and organic ligands, the lattice parameters in a, b, and c directions in the single crystal cells could bring about subtle or large structural difference. It will result in the composite material with distinct growth methods to obtain secondary MOF grown from the initial MOF. In this review, the authors wish to mainly outline the latest synthetic strategies of heterostructured MOF-on-MOFs and their derivatives, including ordered epitaxial growth, random epitaxial growth, etc., which show the tutorial guidelines for the further development of various MOF-on-MOFs.

Growth and antioxidant response in Spirodela polyrrhiza under linear alkylbenzene sulfonate, naphthalene and their joint stress.

The synthetic organic surfactants linear alkylbenzene sulfonate (LAS) and polycyclic aromatic hydrocarbon naphthalene (NAP), two common organic pollutants, are frequently detected in freshwater environments. However, the combined ecotoxicological risks associated with these pollutants have not been fully elucidated. The present study investigated the effects of individual and combined treatments of LAS and NAP on the growth and physiological responses of Spirodela polyrrhiza. The results showed that LAS was the main compound toxic to S. polyrrhiza in a dose-dependent manner. The peroxidase (POD) enzyme and catalase (CAT) enzyme are the main antioxidant enzymes protecting S. polyrrhiza from LAS stress. When exposed to NAP stress alone, only slightly reversible damage was observed as the exposure time was extended (14 days). The antioxidant enzyme systems (including superoxide dismutase (SOD), CAT and POD) showed positive responses. Synergistic effects were induced with LAS-NAP mixtures (≥ 5 + 5 mg L-1), and LAS played a major toxic role. The POD enzyme was a sensitive protective enzyme in duckweed during the joint exposure to LAS + NAP. The results indicate that LAS or NAP may cause serious damage to S. polyrrhiza and aggravate ecotoxicity in aquatic ecosystems.

Sulfur-Induced Growth of Coordination Polymer Derived-Straight Carbon Nanotubes on Carbon Nanofiber Network for Zn-Air Batteries.

Low-cost heteroatom-doped carbon nanomaterials have been widely studied for efficient oxygen reduction reaction and energy storage and conversion in metal-air batteries. A Masson pine twigs-like 3-dimensional network construction of carbon nanofibers (CNFs) with abundant straight long Co, N, and S-doped carbon nanotubes (CNTs) is developed by thermal treatment of Co-based polymer coated onto polyacrylonitrile nanofiber network together with thiourea at 900 °C, denoted as CNFT-Co9 S8 -900. It is interesting to note that the introduction of a high concentration of sulfur does not lead to the complete toxicity of catalysts, but promotes the axial growth to selectively form straight CNTs instead of curly bamboo-like CNTs. The highly graphitized in-situ grown Co, N, S-doped CNTs and the 3-dimensional N-doped CNF network provide both active catalytic sites and highly conductive paths, which are beneficial for oxygen reduction reaction (ORR). Thus, the optimal CNFT-Co9 S8 -900 performs the excellent ORR catalytic activity with a half-wave potential of 0.84 V and a diffusion-limited current density of 5.49 mA cm-2 . Furthermore, the CNFT-Co9 S8 -900-based Zn-air devices also possess a high power density of 136.9 mW cm-2 better than commercial Pt/C.

Hierarchically activated porous carbon derived from zinc-based fluorine containing metal-organic framework as extremely high specific capacitance and rate performance electrode material for advanced supercapacitors.

In this work, a hierarchically activated porous carbon (APC) was synthesized using fluorine-containing metal-organic framework via facile combined carbonization and KOH activation treatments. The influences of activation conditions on the surface structures and electrochemical performance of APC were systematically studied. Afterwards, the electrochemical responses of APC electrode were further assessed from the cyclic voltammetry and galvanostatic charge-discharge examinations by 6 M KOH electrolyte. The as-obtained APC electrode delivered the high specific capacitances of 540.8 and 280 F g-1 at 1 and 500 A g-1, correspondingly with superior capacitance retention of 94% after 250,000 cycles even at 100 A g-1, which is showing that its outstanding capacitance, remarkable rate capacity, and very-long cyclic life. Furthermore, the as-assembled APC-based symmetrical supercapacitor offers a superb energy density of 19 Wh kg-1 at 182 W kg-1, indicating its large-scale application. Thus, this work proposes a potential route to synthesize highly efficient porous carbon material for the future development of energy storage systems.

Visible-Light-Induced Nickel-Catalyzed P(O)-C(sp2) Coupling Using Thioxanthen-9-one as a Photoredox Catalysis.

An efficient method has been developed for photocatalytic P(O)-C(sp2) coupling of (hetero)aryl halides with H-phosphine oxides or H-phosphites under the irradiation of visible light or sunlight. The thioxanthen-9-one/nickel dual catalysis mediates this phosphonylation to give arylphosphine oxides and arylphosphonates in moderate to excellent yields. This transformation is widely tolerant to a range of functional groups and proceeds efficiently on a gram scale.

Surfactant-Mediated Morphological Evolution of MnCo Prussian Blue Structures.

In the preparation of nanomaterials, the kinetics and thermodynamics in the reaction can significantly affect the structures and phases of nanocrystals. Therefore, people are keen to adopt various synthetic strategies to accurately assemble the target nanocrystals, and reveal the underlying mechanism of the formation of specific structures. In this work, the total reaction time is adjusted to let the prepared MnCo Prussian blue analogous (MnCoPBA) crystals show four evolving morphological changes at different stages with the assistance of sodium dodecyl sulfate. Furthermore, it is clearly observed that the epitaxial growth along the (100) plane on the shell of MnCoPBA nanocrystals is favored, and the thermodynamics and kinetics in the morphology change process are analyzed in detail. Through the simple pyrolysis, MnCoPBA crystals can be successfully converted into the corresponding carbon composites, of which Mn2 Co2 C nanoparticles are evenly distributed in highly graphitized carbon matrix. Among them, PBA-III-700 performs good oxygen reduction reaction performance in alkaline solution with the half-wave potential of 0.801 V and diffusion-limited current density of 5.36 mA cm-2 , and its zinc-air battery exhibits the peak power density of 103.4 mW cm-2 competitive with commercial Pt/C.

Correction: Non-toxic dose of liposomal honokiol suppresses metastasis of hepatocellular carcinoma through destabilizing EGFR and inhibiting the downstream pathways.

[This corrects the article DOI: 10.18632/oncotarget.13687.].

Rapid and Controllable Synthesis of Nanocrystallized Nickel-Cobalt Boride Electrode Materials via a Mircoimpinging Stream Reaction for High Performance Supercapacitors.

Nickel-cobalt borides (denoted as NCBs) have been considered as a promising candidate for aqueous supercapacitors due to their high capacitive performances. However, most reported NCBs are amorphous that results in slow electron transfer and even structure collapse during cycling. In this work, a nanocrystallized NCBs-based supercapacitor is successfully designed via a facile and practical microimpinging stream reactor (MISR) technique, composed of a nanocrystallized NCB core to facilitate the charge transfer, and a tightly contacted Ni-Co borates/metaborates (NCBi ) shell which is helpful for OH- adsorption. These merits endow NCB@NCBi a large specific capacity of 966 C g-1 (capacitance of 2415 F g-1 ) at 1 A g-1 and good rate capability (633.2 C g-1 at 30 A g-1 ), as well as a very high energy density of 74.3 Wh kg-1 in an asymmetric supercapacitor device. More interestingly, it is found that a gradual in situ conversion of core NCBs to nanocrystallized Ni-Co (oxy)-hydroxides inwardly takes place during the cycles, which continuously offers large specific capacity due to more electron transfer in the redox reaction processes. Meanwhile, the electron deficient state of boron in metal-borates shells can make it easier to accept electrons and thus promote ionic conduction.