Construction of the Fast Potassiation Path in Sbx Bi1-x @NC Anode with Ultrahigh Cycling Stability for Potassium-Ion Batteries.

Due to the scarce of lithium resources, potassium-ion batteries (PIBs) have attracted extensive attention due to their similar electrochemical properties to lithium-ion batteries (LIBs) and more abundant potassium resources. Even though there is considerable progress in SbBi alloy anode for LIBs and PIBs, most studies are focused on the morphology/structure tuning, while the inherent physical features of alloy composition's effect on the electrochemical performance are rarely investigated. Herein, combined the nanonization, carbon compounding, and alloying with composition regulation, the anode of nitrogen-doped carbon-coated Sbx Bi1-x (Sbx Bi1-x @NC) with a series of tuned chemical compositions is designed as an ideal model. The density functional theory (DFT) calculation and experimental investigation results show that the K+ diffusion barrier is lower and the path is easier to carry out when element Bi dominates the potassiation reaction, which is also the reason for better circulation. The optimized Sb0.25 Bi0.75 @NC shows an excellent cycling performance with a reversible specific capacity of 301.9 mA h g-1 after 500 cycles at 0.1 A g-1 . Meanwhile, the charge-discharge mechanism is intuitively invetigated and analyzed by in situ X-ray diffraction (XRD) and transmission electron microscopy (TEM) in detail. Such an alloy-type anode synthesis approach and in situ observation method provide an adjustable strategy for the designing and investigating of PIB anodes.

Effect of DHCR7 for the co-occurrence of hypercholesterolemia and vitamin D deficiency in type 2 diabetes: Perspective of health prevention.

Type 2 diabetes mellitus (T2DM) is a complex disease caused by multiple factors, which are often accompanied by the disorder of glucose and lipid metabolism and the lack of vitamin D.Over the years, researchers have conducted numerous studies into the pathogenesis and prevention strategies of diabetes. In this study, diabetic SD rats were randomly divided into type 2 diabetes group, vitamin D intervention group, 7-dehydrocholesterole reductase (DHCR7) inhibitor intervention group, simvastatin intervention group, and naive control group. Before and 12 weeks after intervention, liver tissue was extracted to isolate hepatocytes. Compared with naive control group, in the type 2 diabetic group without interference, the expression of DHCR7 increased, the level of 25(OH)D3 decreased, the level of cholesterol increased. In the primary cultured naive and type 2 diabetic hepatocytes, the expression of genes related to lipid metabolism and vitamin D metabolism were differently regulated in each of the 5 treatment groups. Overall, DHCR7 is an indicator for type 2 diabetic glycolipid metabolism disorder and vitamin D deficiency. Targeting DHCR7 will help with T2DM therapy.The management model of comprehensive health intervention can timely discover the disease problems of diabetes patients and high-risk groups and reduce the incidence of diabetes.

Muscone attenuates susceptibility to ventricular arrhythmia by inhibiting NLRP3 inflammasome activation in rats after myocardial infarction.

Fibrosis and abnormal expression of connexin 43 (Cx43) in the ventricle play vital roles in ventricular arrhythmias (VAs) after myocardial infarction (MI). Muscone, an active monomer of heart-protecting musk pill, has various biological activities, but its effect on susceptibility to VAs in rats with MI has not been determined. In the present study, we investigated the effects of muscone on ventricular inflammation, fibrosis, Cx43 expression, and the occurrence of VAs after MI. An MI model was established by ligating the proximal left anterior descending coronary artery. Then, the MI model rats were administered muscone (2 mg/kg/day) or vehicle (saline)via intragastric injection for 14 days. Cardiac function was evaluated by echocardiography, and an in vivo electrophysiological study was performed on Day 14. Cardiac inflammation, fibrosis, and Cx43 expression were determined by histochemical analysis and western blot analysis. Our results indicated that muscone treatment significantly improved cardiac function and inhibited ventricular inflammation, fibrosis, and nucleotide-binding oligomerization domain, leucine-rich repeat, and pyrin domain containing 3 (NLRP3) inflammasome activation. Electrocardiogrphy and electrophysiology studies showed that muscone shortened the QRS interval, QT interval, QTc interval, and action potential duration; prolonged the effective refractory period; and reduced susceptibility to VAs in rats after MI. Furthermore, Cx43 expression in the BZ was increased by muscone treatment, and this change was coupled by inhibition of the NLRP3/IL-1ß/p38 MAPK pathway. Taken together, our results demonstrated that muscone reduces susceptibility to VA, mainly by decreasing ventricular inflammation and fibrosis, and attenuates abnormal Cx43 expression by inhibiting NLRP3 inflammasome activation after myocardial infarction in rats.

One-Step Preparation of a Superhydrophobic Surface by Electric Discharge Machining with a Carbon Fiber Brush Electrode.

Superhydrophobic surfaces are extremely susceptible to damage, which can lead to a sharp decrease in their service life and physical properties. Therefore, developing methods to impart superhydrophobic surfaces with excellent wear resistance is crucial. In this article, a flexible carbon fiber brush was utilized as an electrode to fabricate micro-/nano-structures on a grooved surface via electric discharge machining in one step, resulting in a superhydrophobic coating with excellent wear resistance. Carbon fiber brushes exhibit several notable properties, including excellent flexibility, conductivity, and high temperature resistance. Carbon fiber brushes can adapt to the complex inner walls of grooves. Many nano-structures were fabricated on the grooves via pulse discharge, which resulted in a superhydrophobic surface with excellent wear resistance. The contact angle (CA) and sliding angle of the surface after discharge were 156.3 and 2°, respectively. The processed surface exhibits superior corrosion resistance compared to the stainless-steel substrate. The influence of the micro-groove shapes on wear resistance was tested. The results showed that, after 500 cm of wear, the shallow grooves retained their superhydrophobicity with a CA of 150.1°.

Breaking the Passivation: Sodium Borohydride Synthesis by Reacting Hydrated Borax with Aluminum.

A significant obstacle in the large-scale applications of sodium borohydride (NaBH4 ) for hydrogen storage is its high cost. Herein, we report a new method to synthesize NaBH4 by ball milling hydrated sodium tetraborate (Na2 B4 O7 ⋅ 10H2 O) with low-cost Al or Al88 Si12 , instead of Na, Mg or Ca. An effective strategy is developed to facilitate mass transfer during the reaction by introducing NaH to enable the formation of NaAlO2 instead of dense Al2 O3 on Al surface, and by using Si as a milling additive to prevent agglomeration and also break up passivation layers. Another advantage of this process is that hydrogen in Na2 B4 O7 ⋅ 10H2 O serves as a hydrogen source for NaBH4 generation. Considering the low cost of the starting materials and simplicity in operation, our studies demonstrate the potential of producing NaBH4 in a more economical way than the commercial process.

One-Step Preparation of Robust Superhydrophobic Foam for Oil/Water Separation by Pulse Electrodeposition.

Frequent leakage and pollution of oily wastewater seriously affect the world's ecosystem safety and economic development, which prompts us to urgently develop a highly effective, low-cost, wear-resistant, chemically stable, and environmentally friendly new functional material for oil/water separation. In this paper, a robust superhydrophobic material was successfully electrodeposited on the porous copper foam substrates in myristic acid (CH3(CH2)12COOH) and lanthanum chloride (LaCl3·6H2O) electrodeposition solution under a continuous pumping circulation and rotation condition. Moreover, SEM, EDS, XRD, FTIR, and XPS technologies were utilized to characterize the surface morphology and chemical composition information. The superhydrophobic property was evaluated by optical contact angle instrument and high-speed camera. It turned out that the micro/nanostructures were mainly composed of lanthanum myristate, and static CA of superhydrophobic copper foam (SCF) was up to 165.2° with SA ≈ 2°. Besides, the SCF exhibited a better performance with good anticorrosion, excellent chemical stability, and outstanding mechanical stability. Furthermore, the SCF can achieve up to 98.6% oil/water separation efficiency. More importantly, by employing this novel processing method, it can effectively save time and provide a promising potential way to make denser and thicker foams for continuous oil/water separation and may be easily applied to other conductive metal matrix materials.

LncRNA MALAT1 regulates diabetic cardiac fibroblasts through the Hippo-YAP signaling pathway.

Diabetic cardiomyopathy (DCM) is a major diabetes-related microvascular disease. LncRNA MALAT1 is widely expressed in cardiomyocytes responding to hypoxia and high levels of glucose (high glucose). In this study, cardiac fibroblasts (CFs) were transfected with si-MALAT1 and exposed to high glucose. CFs in the high glucose groups were treated with 30 mmol/L glucose, and the control CFs were treated with 5.5 mmol/L glucose. The expression of MALAT1 in the nucleus and cytoplasm of CFs was detected. The biological behavior of CFs, as well as collagen production, activity of the Hippo-YAP pathway, and nuclear localization of YAP were measured. Mouse models of DCM were established to observe the pathological changes to myocardium and determine the levels of collagen I, Bax, and Bcl-2. The interaction between MALAT1 and YAP was analyzed, and CREB expression in the high-glucose treated CFs was detected. MALAT1 was upregulated in high-glucose CFs and located in the nucleus. High-glucose increased collagen production, inflammation, cell proliferation, cell invasiveness, and phosphorylation of MST1 and LATS1, and also promoted nuclear translocation of YAP. These trends in high-glucose treated CFs and the DCM mice were reversed by transfection with si-MALAT1. MALAT1 positively regulated the nuclear translocation of YAP by binding to CREB. CREB levels were increased in the high-glucose CFs, but decreased after silencing MALAT1. These results indicate that si-MALAT1 reduces inflammation and collagen accumulation in high-glucose CFs and DCM mice via the Hippo-YAP pathway and CREB.

Closing the Loop for Hydrogen Storage: Facile Regeneration of NaBH4 from its Hydrolytic Product.

Sodium borohydride (NaBH4 ) is among the most studied hydrogen storage materials because it is able to deliver high-purity H2 at room temperature with controllable kinetics via hydrolysis; however, its regeneration from the hydrolytic product has been challenging. Now, a facile method is reported to regenerate NaBH4 with high yield and low costs. The hydrolytic product NaBO2 in aqueous solution reacts with CO2 , forming Na2 B4 O7 ⋅10 H2 O and Na2 CO3 , both of which are ball-milled with Mg under ambient conditions to form NaBH4 in high yield (close to 80 %). Compared with previous studies, this approach avoids expensive reducing agents such as MgH2 , bypasses the energy-intensive dehydration procedure to remove water from Na2 B4 O7 ⋅10 H2 O, and does not require high-pressure H2 gas, therefore leading to much reduced costs. This method is expected to effectively close the loop of NaBH4 regeneration and hydrolysis, enabling a wide deployment of NaBH4 for hydrogen storage.

Dramatically Enhanced Li-Ion Storage of ZnO@C Anodes through TiO2 Homogeneous Hybridization.

Amorphous nanoparticles of ZnO and TiO2 embedded in carbon nanocages (AZT⊂CNCs) were successfully synthesized through a simple annealing process of TiO2 -coated zeolitic imidazolate framework-8 (ZIF-8). In the current anode of AZT⊂CNCs, tiny ZnO and TiO2 nanoparticles were uniformly distributed in the carbon matrix (carbon nanocages), which could effectively buffer the volume expansion of electroactive ZnO and provide excellent electric conductivity. After fully investigating the electrochemical performance of the AZT⊂CNCs samples obtained with different additive amounts of tetrabutyl orthotitanate (TBOT) for TiO2 coating, it has been found that AZT-30 (0.1 g ZIF-8 with 30 mL TBOT) shows the best cycle stability (510 mA h g-1 after 350 cycles at 200 mA g-1 ) and a superior rate capability (610 mA h g-1 after 3500 cycles at 2 A g-1 ). The greatly enhanced Li-ion storage performance could be ascribed to the fact that the introduction of amorphous TiO2 could activate the reversible lithiation/delithiation reaction of ZnO during the charge/discharge process.

Controllable Hydrolysis Performance of MgLi Alloys and Their Hydrides.

Theoretically, the hydrolysis of MgLi and MgH2 -LiH can produce 9.6 and 17.5 wt.% hydrogen (water is not included in the calculation), respectively. The ball-milling method is commonly used to refine the particle size and thus may improve hydrolysis kinetics. However, Mg and Li will be easily agglomerated, which means that direct ball-milling could not refine MgLi. In this work, we introduced 10 wt.% expanded graphite into the ball-milling process to synthesize refined MgLi alloy samples. Further studies showed that MgLi-10 wt.% expanded graphite can produce 966 mL/g hydrogen within 3 min in 0.5 M MgCl2 solution. The MgLi hydrides were synthesized by reactive ball milling under 3 MPa H2 and their hydrolysis performance was investigated. Moreover, the sawed powder was milled in 3 MPa H2 for 6 h and then hydrogenated in 3 MPa H2 at 380 °C; it can produce 1542 and 1773 mL/g (15.8 wt.%) hydrogen in 5 and 30 min with mild kinetics, respectively, and the activation energy of the hydrolysis reaction is 24.6 kJ/mol in 1 M MgCl2 solution. The findings here open a new avenue to the development of refined MgLi alloys and hydrides for hydrogen generation through a controllable hydrolysis process.

FeP@C Nanotube Arrays Grown on Carbon Fabric as a Low Potential and Freestanding Anode for High-Performance Li-Ion Batteries.

An anode of self-supported FeP@C nanotube arrays on carbon fabric (CF) is successfully fabricated via a facile template-based deposition and phosphorization route: first, well-aligned FeOOH nanotube arrays are simply obtained via a solution deposition and in situ etching route with hydrothermally crystallized (Co,Ni)(CO3 )0.5 OH nanowire arrays as the template; subsequently, these uniform FeOOH nanotube arrays are transformed into robust carbon-coated Fe3 O4 (Fe3 O4 @C) nanotube arrays via glucose adsorption and annealing treatments; and finally FeP@C nanotube arrays on CF are achieved through the facile phosphorization of the oxide-based arrays. As an anode for lithium-ion batteries (LIBs), these FeP@C nanotube arrays exhibit superior rate capability (reversible capacities of 945, 871, 815, 762, 717, and 657 mA h g-1 at 0.1, 0.2, 0.4, 0.8, 1.3, and 2.2 A g-1 , respectively, corresponding to area specific capacities of 1.73, 1.59, 1.49, 1.39, 1.31, 1.20 mA h cm-2 at 0.18, 0.37, 0.732, 1.46, 2.38, and 4.03 mA cm-2 , respectively) and a stable long-cycling performance (a high specific capacity of 718 mA h g-1 after 670 cycles at 0.5 A g-1 , corresponding to an area capacity of 1.31 mA h cm-2 at 0.92 mA cm-2 ).

Nanoconfined Oxidation Synthesis of N-Doped Carbon Hollow Spheres and MnO2 Encapsulated Sulfur Cathode for Superior Li-S Batteries.

The sulfur cathode, as a new generation of lithium-ion battery cathode material, has a high theoretical energy density of about 2500 Wh kg-1 . However, the low conductivity of sulfur and the "shuttle effect", widely presenting in the lithiation/de-lithiation process, seriously hinder its practical application. Here, we report a new nanoconfined oxidation route (first complete oxidation of metal sulfide and subsequently partial oxidation of the generated S from sulfide) for S cathode encapsulated with MnO2 nanosheets and N-doped carbon hollow spheres. This nanoconfined oxidation route can successfully confine the sulfur particles in the interior of the carbon shell, and the rationally introduced nonpolar carbon and polar MnO2 can both reduce the dissolution of polysulfide during the charge-discharge process. The obtained well-defined S-MnO2 @C cathode exhibits high specific capacity with excellent cycling performance and superior rate capability.

New Nanoconfined Galvanic Replacement Synthesis of Hollow Sb@C Yolk-Shell Spheres Constituting a Stable Anode for High-Rate Li/Na-Ion Batteries.

In the current research project, we have prepared a novel Sb@C nanosphere anode with biomimetic yolk-shell structure for Li/Na-ion batteries via a nanoconfined galvanic replacement route. The yolk-shell microstructure consists of Sb hollow yolk completely protected by a well-conductive carbon thin shell. The substantial void space in the these hollow Sb@C yolk-shell particles allows for the full volume expansion of inner Sb while maintaining the framework of the Sb@C anode and developing a stable SEI film on the outside carbon shell. As for Li-ion battery anode, they displayed a large specific capacity (634 mAh g-1), high rate capability (specific capabilities of 622, 557, 496, 439, and 384 mAh g-1 at 100, 200, 500, 1000, and 2000 mA g-1, respectively) and stable cycling performance (a specific capacity of 405 mAh g-1 after long 300 cycles at 1000 mA g-1). As for Na-ion storage, these yolk-shell Sb@C particles also maintained a reversible capacity of approximate 280 mAh g-1 at 1000 mA g-1 after 200 cycles.

Self-Supported CoP Nanorod Arrays Grafted on Stainless Steel as an Advanced Integrated Anode for Stable and Long-Life Lithium-Ion Batteries.

To alleviate the capacity degradation of anode materials for Li-ion batteries, caused by serious volume expansion and particle aggregation, intensive attention has been devoted to the rational design and fabrication of novel anode architectures. Herein, self-supported CoP nanorod arrays have been facilely synthesized using hydrothemally deposited Co(CO3 )0.5 (OH)⋅0.11 H2 O nanorod arrays as the precursor, through a gas-phase phosphidation method. As the anode for Li-ion batteries, such 3D interconnected CoP nanorod arrays show an initial discharge capacity of 1067 mAh g-1 and a high reversible charge capacity of 737 mAh g-1 at 0.4 Ag-1 . After 400 cycles, their specific capacity can reach 510 mAh g-1 ; even after 900 cycles, they can still deliver a specific capacity of 390 mAh g-1 . CoP//LiCoO2 full-cells also exhibit a high reversible capacity of 400 mAh g-1 after 50 cycles. These unique 3D interconnected CoP nanorod arrays also show ultrastable cycling performance over 500 cycles when used as the anode in a Na-ion battery.

Exfoliation of MoS2 and h-BN nanosheets by hydrolysis of LiBH4.

Efficient preparation of two-dimensional materials is still a great challenge. These materials possess unique electrical, optical, and thermal properties. In this study, few-layer MoS2 nanosheets and nanoflakes were exfoliated by the hydrolysis reaction of LiBH4. First, the layered MoS2 powder materials were mixed with LiBH4 to obtain a homogeneous powder mixture, and then the mixture was heated above the melting point of LiBH4 under 300 °C and 4 MPa H2 for 2 h, during which the layered materials were curled by liquid LiBH4. In the subsequent hydrolysis of LiBH4, the layered materials were split into nanosheets by H2 gas generation. The obtained MoS2 nanosheets show almost uniform thickness of ~4 nm, with a width of 2-10 µm and a yield of more than 1.5 wt.%. The effectiveness of this method has also been verified by the preparation of few-layer h-BN. This work provides a new high-yield route to producing two-dimensional materials.

Tuning Electro-Optical Characteristics through Polymerization Monomer Content in PSVA Liquid Crystal Displays: Simulation and Experimentation.

The enhancement of display performance and durability in polymer-stabilized vertical alignment liquid crystal and the liquid crystal are negative liquid crystals, which can be vertically aligned under the action of a vertical orientation layer and an electric field. Devices (PSVA LCDs) are crucial for advancing LCD technology. This study aims to investigate the electro-optical characteristics of PSVA LCDs by varying polymerization monomer concentrations. Using both simulations via TechWiz LCD 3D and experimental methods, such as polymer-induced phase separation, we developed an optoelectronic testing framework to assess voltage transmittance and response times. In our main findings, we show that an increase in polymeric monomer concentration from 3% to 7% resulted in a 67% increase in threshold voltage and a 44% decrease in saturation voltage. The on-state response time increased by about a factor of three, while the off-state response time decreased by about a factor of three. The alignment of our simulation results with experimental data validates our methodology, offering the potential of simulation tools as a pivotal resource in the PSVA LCDs. The alignment of our simulation results with experimental data validates our methodology, offering the potential of simulation tools as a pivotal resource in the PSVA LCDs. These advancements promise significant improvements in PSVA LCD performance and durability.

Room-Temperature Transient Hydrogen Uptake of MgH2 Induced by Nb-Doped TiO2 Solid-Solution Catalysts.

The practical applications of MgH2 as a high-density hydrogen carrier depend heavily on efficient and low-cost catalysts to accelerate the dehydriding/hydriding reactions at moderate temperatures. In the present work, this issue is addressed by synthesizing Nb-doped TiO2 solid-solution-type catalysts that dramatically improve the hydrogen sorption performances of MgH2. The catalyzed MgH2 can absorb 5 wt % of H2 even at room temperature for 20 s, release 6 wt % of H2 at 225 °C within 12 min, and the complete dehydrogenation can be achieved at 150 °C under a dynamic vacuum atmosphere. Density functional theory calculations reveal that Nb doping introduces Nb 4d orbitals with stronger interaction with H 1s into the density of states of TiO2. This considerably enhances both the adsorption and dissociation ability of the H2 molecule on the catalysts surface and the hydrogen diffusion across the specific Mg/Ti(Nb)O2 interface. The successful implementation of solid solution-type catalysts in MgH2 offers a demonstration and inspiration for the development of high-performance catalysts and solid-state hydrogen storage materials.

Phloretin ameliorates heart function after myocardial infarction via NLRP3/Caspase-1/IL-1ß signaling.

OBJECTIVES/AIMS: Inflammation is crucial in structural and electrical remodeling after myocardial infarction (MI), affecting cardiac pump function and conduction pathways. Phloretin possesses an anti-inflammation role by inhibiting the NLRP3/Caspase-1/IL-1ß pathway. However, the effects of Phloretin on cardiac contractile and electrical conduction function after MI remained unclear. Therefore, we aimed to investigate the potential role of Phloretin in a rat model of MI. METHODS: Rats were assigned into four groups: Sham, Sham+Phloretin, MI and MI+Phloretin, with ad libitum food and water. In the MI and MI+Phloretin groups, the left anterior descending coronary artery was occluded for 4 weeks, while the Sham and Sham+Phloretin groups received sham operation. The Sham+Phloretin group and the MI+Phloretin group received oral administration of Phloretin. In vitro, H9c2 cells were subjected to hypoxic conditions to simulate an MI model, with Phloretin for 24 h. Cardiac electrophysiological properties were assessed following MI, including the effective refractory period (ERP), action potential duration (APD)90 and ventricular fibrillation (VF) incidence. Echocardiography evaluated left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), left ventricular internal diameter at end-diastole (LVIDd), left ventricular internal diameter at end-systole (LVIDs), left ventricular end-systolic volume (LVESV) and left ventricular end-diastolic volume (LVEDV) to assess cardiac function. Serum type B natriuretic peptide (BNP) level was applied to evaluate the degree of Heart failure (HF). The fibrosis area and severity were assessed by Masson staining and protein expression levels of collagen 3, collagen 1, TGF-ß and α-SMA. Western blot analysis estimated the protein expression levels of NLRP3, Pro Caspase-1, Caspase-1, ASC, IL-18, IL-1ß, pp38, p38, and Connexin43(Cx43) to elucidate the influence of inflammation on electrical remodeling after MI. RESULTS: Our findings demonstrate that Phloretin inhibits the NLRP3/Caspase-1/IL-1ß pathway, leading to the upregulation of Cx43 by limiting p38 phosphorylation, which further decreases susceptibility to ventricular arrhythmias (VAs). Additionally, Phloretin attenuated fibrosis by inhibiting inflammation to prevent HF. In vitro experiments also provided strong evidence supporting the inhibitory effects of Phloretin on the NLRP3/Caspase-1/IL-1ß pathway. CONCLUSION: Our results suggest that Phloretin could suppress the NLRP3/Caspase-1/IL-1ß pathway to reverse structural and electrical remodeling after MI to prevent the occurrence of VAs and HF.

In Situ Formation of Li2SiO3-Li-NaCl Interface on Si and Its Effect on Hydrogen Evolution.

Silicon has emerged as a competitive candidate for hydrolytic hydrogen production due to its high theoretical hydrogen yield, low cost, and on-demand availability. However, the hydrolysis reaction is extremely restrained by passivated SiO2, including the original one on the Si surface and the generated one during hydrolysis, and almost no hydrogen is produced in pure water. Herein, the original SiO2 surface has been effectively removed by milling micro-Si mixed with a small amount of Li metal and NaCl. An artificial soluble interface on Si has been established containing Li2SiO3, Li, and NaCl. Once micro-Si is placed into water, fresh Si surface can be exposed and a weak LiOH solution can be generated due to the fast dissolution of the interface layer, resulting in the rapid liberation of hydrogen gas. Accordingly, the modified micro-Si displays a significantly enhanced hydrogen production in pure water at 30 °C (1213 mL g-1 H2 within 3.0 h), which is 2.0 and 4.7 times higher than that observed for ball-milled Si and raw Si in 0.06 M LiOH solution, respectively. In addition, it also exhibited an outstanding operation compatibility for practical uses. This work has proposed a green, effective, and scalable strategy to promote hydrogen production from the hydrolysis of Si-based systems.

Composite dietary antioxidant index and the risk of heart failure: A cross-sectional study from NHANES.

BACKGROUND: Previous studies show that oxidative stress is important in heart failure (HF) pathogenesis. The composite dietary antioxidant index (CDAI), which reflects the antioxidant profile of nutrient supplements, is associated with cardiovascular mortality risk. However, the association between CDAI and the risk of HF remains unknown. HYPOTHESIS: In this study, we investigated the relationship between CDAI and HF risk using National Health and Nutritional Examination Survey (NHANES) data. METHODS: The data of participants aged >40 years old from the NHNANES between 2001 and 2018 were obtained and used to assess the relationship between CDAI and the risk of HF. Logistic regression was used to calculate the odds ratio (OR) of CDAI for the risk of HF. RESULTS: A total of 29 101 participants were divided into the HF (n = 1419; 4.88%) and non-HF groups (n = 27 682; 95.12%), HF group participants had lower CDAI than the non-HF group (-0.32 ± 0.14 vs. 0.67 ± 0.05, p < .0001). Compared with the lowest CDAI quartile (Q1), the OR for HF risk was 0.88 (0.68-1.13) for Q2 (p = .30), 0.77 (0.61-0.99) for Q3 (p = .04), and 0.68 (0.52-0.89) for Q4 (p = .01). CONCLUSIONS: CDAI was negatively associated with the risk of HF. Our findings show that the intake of an antioxidant-rich dietary is a potential method to reduce the risk of HF.