Hierarchical Nanoheterostructure of HFIP-Grafted α-Fe2O3@Multiwall Carbon Nanotubes as High-Performance Chemiresistive Sensors for Nerve Agents.

New and efficient sensors of nerve agents are urgently demanded to prevent them from causing mass casualties in war or terrorist attacks. So, in this work, a novel hierarchical nanoheterostructure was synthesized via the direct growth of α-Fe2O3 nanorods onto multiwall carbon nanotube (MWCNT) backbones. Then, the composites were functionalized with hexafluoroisopropanol (HFIP) and successfully applied to detect dimethyl methylphosphonate (DMMP)-sarin simulant gas. The observations show that the HFIP-α-Fe2O3@MWCNT hybrids exhibit outstanding DMMP-sensing performance, including low operating temperature (220 °C), high response (6.0 to 0.1 ppm DMMP), short response/recovery time (8.7 s/11.9 s), as well as low detection limit (63.92 ppb). The analysis of the sensing mechanism demonstrates that the perfect sensing performance is mainly due to the synergistic effect of the chemical interaction of DMMP with the heterostructure and the physical adsorption of DMMP by hydrogen bonds with HFIP that are grafted on the α-Fe2O3@MWCNTs composite. The huge specific surface area of HFIP-α-Fe2O3@MWCNTs composite is also one of the reasons for this enhanced performance. This work not only offers a promising and effective method for synthesizing sensitive materials for high-performance gas sensors but also provides insight into the sensing mechanism of DMMP.

Regulation of Cervical Cancer Development by a Novel Circ_0000212/miR-1236-3p/GREM1 ceRNA Crosstalk.

Circular RNAs (circRNAs) possess important functions in cervical carcinogenesis by operating as competing endogenous RNAs (ceRNAs). Our preliminary bioinformatics predicted the potential circ_0000212/microRNA (miR)-1236-3p/gremlin 1 (GREM1) ceRNA crosstalk. Thus, we further elucidated whether the novel ceRNA crosstalk can participate in cervical cancer development. Circ_0000212, miR-1236-3p and GREM1 were quantified by real-time quantitative polymerase chain reaction (qPCR) and immunoblotting. 5-ethynyl-2'-deoxyuridine (EdU) assay, flow cytometry, and tube formation assay were performed to assess cell proliferation, apoptosis and tube formation, respectively. Transwell assay was used to detect cell migration and invasion. Mouse xenografts were established to evaluate the role of circ_0000212 in vivo. Dual-luciferase reporter assay was performed to verify the direct relationship between miR-1236-3p and circ_0000212 or GREM1. Circ_0000212 expression was elevated in human cervical cancer. Silencing of endogenous circ_0000212 hindered cancer cell proliferation, motility and invasion and induced apoptosis, as well as diminished the tube formation of human umbilical vein endothelial cells (HUVECs) in vitro. Circ_0000212 silencing also weakened tumor growth in vivo. Mechanistically, circ_0000212 directly bound to miR-1236-3p, and downregulation of miR-1236-3p reversed these effects of circ_0000212 silencing on cell malignant phenotypes and HUVEC tube formation. GREM1 was a direct miR-1236-3p target, and its expression was regulated by circ_0000212 through miR-1236-3p. Moreover, miR-1236-3p upregulation impeded cancer cell malignant phenotypes and HUVEC tube formation by targeting GREM1. Our findings identify a novel ceRNA regulatory network, circ_0000212/miR-1236-3p/GREM1 axis, in cervical carcinogenesis, and provide potential targets that can be explored for therapeutic interventions.

Surface hydrolysis-anchored eugenol self-polishing marine antifouling coating.

Traditional self-polishing antifouling coatings kill surface organisms by releasing toxic substances, which are damaging to the ecosystem. As a natural antimicrobial substance, eugenol is environmentally friendly and has been proven by different research teams to be effective in enhancing the anti-fouling effect of coatings in the real sea. While in these previous research works, the eugenol was released directly into the seawater thus cannot further serve as surface antifouling effect, leading to a limited antifouling effect of the coating. In this work, the quaternary ammonium component was introduced into the butyl ester-based resin - poly (eugenol methacrylate - acryloyloxyethyltrimethyl ammonium chloride - hexafluorobutyl methacrylate - methyl methacrylate - butyl methacrylate - ethylene glycol methyl ether acrylate) (EMQFP) coating for the first time by simple one-step free radical polymerization method. On the one hand, the eugenol produced by hydrolysis is anchored to the quaternary ammonium on the coating surface for a period of time due to the cationic-π interaction, instead of being released into seawater immediately after hydrolysis, thus increasing the utilization rate of eugenol; on the other hand, the negatively charged carboxylate groups generated after hydrolysis in the coating are mutually attracted to quaternary ammonium through electrostatic effect, so the resin chain segment conformation on the coating surface adjusted to produce zwitterionic-like structure, and the hydration of zwitterionic inhibits primary fouling adhesion.

Frequency Stability Prediction of Power Systems Using Vision Transformer and Copula Entropy.

This paper addresses the problem of frequency stability prediction (FSP) following active power disturbances in power systems by proposing a vision transformer (ViT) method that predicts frequency stability in real time. The core idea of the FSP approach employing the ViT is to use the time-series data of power system operations as ViT inputs to perform FSP accurately and quickly so that operators can decide frequency control actions, minimizing the losses caused by incidents. Additionally, due to the high-dimensional and redundant input data of the power system and the O(N2) computational complexity of the transformer, feature selection based on copula entropy (CE) is used to construct image-like data with fixed dimensions from power system operation data and remove redundant information. Moreover, no previous FSP study has taken safety margins into consideration, which may threaten the secure operation of power systems. Therefore, a frequency security index (FSI) is used to form the sample labels, which are categorized as "insecurity", "relative security", and "absolute security". Finally, various case studies are carried out on a modified New England 39-bus system and a modified ACTIVSg500 system for projected 0% to 40% nonsynchronous system penetration levels. The simulation results demonstrate that the proposed method achieves state-of-the-art (SOTA) performance on normal, noisy, and incomplete datasets in comparison with eight machine-learning methods.

Surface morphology properties and antifouling activity of Bi2WO6/boron-grafted polyurethane composite coatings realized via multiple synergy.

An inorganic-organic composite coating is an effective way to solve the issue of marine organism attachment and realize multi-element synergistic antifouling. Herein, Bi2WO6/boron-grafted polyurethane composite coatings (BWOB) composed of Bi2WO6 with three morphologies (nanosheet, flower and microsphere) and boron-grafted polyurethane (ITB) were successfully synthesized to achieve high-efficiency antifouling. Bi2WO6 nanoparticles were evenly distributed on the surface and inside the ITB to form micro/nanostructures. In the composite coatings doped with flower-shaped Bi2WO6, BWOB-5 showed excellent antibacterial and antidiatom adhesion properties, achieving 95.43% and 98.38% against Escherichia coli and Staphylococcus aureus, respectively, and 98.62% against Nitzschia closterium. In addition, the micro/nanostructure on the surface, the stable production of hydroxyl radicals (·OH) and superoxide radicals (·O2-) during photocatalysis, and the antifouling functional groups of the resin matrix in the BWOB composite coatings were all conducive to photocatalytic antifouling activity. More importantly, BWOB coatings exhibited excellent environmentally friendly properties. Therefore, BWOB coatings are expected to have potential application value in the field of photocatalytic sterilization and antifouling.

Theory-Guided Design of a Method to Obtain Competitive Balance between U(VI) Adsorption and Swaying Zwitterion-Induced Fouling Resistance on Natural Hemp Fibers.

The competitive balance between uranium (VI) (U(VI)) adsorption and fouling resistance is of great significance in guaranteeing the full potential of U(VI) adsorbents in seawater, and it is faced with insufficient research. To fill the gap in this field, a molecular dynamics (MD) simulation was employed to explore the influence and to guide the design of mass-produced natural hemp fibers (HFs). Sulfobetaine (SB)- and carboxybetaine (CB)-type zwitterions containing soft side chains were constructed beside amidoxime (AO) groups on HFs (HFAS and HFAC) to form a hydration layer based on the terminal hydrophilic groups. The soft side chains were swayed by waves to form a hydration-layer area with fouling resistance and to simultaneously expel water molecules surrounding the AO groups. HFAS exhibited greater antifouling properties than that of HFAO and HFAC. The U(VI) adsorption capacity of HFAS was almost 10 times higher than that of HFAO, and the max mass rate of U:V was 4.3 after 35 days of immersion in marine water. This paper offers a theory-guided design of a method to the competitive balance between zwitterion-induced fouling resistance and seawater U(VI) adsorption on natural materials.

Synergistically Improved Antifouling Efficiency of a Bioinspired Self-renewing Interface via a Borneol/ Boron Acrylate Polymer.

Underwater facilities are often perplexed by severe and ubiquitous biofouling. The widely applied commercial antifouling materials still have several challenges in static applications. Herein, a polymer containing isoborneol and borane (PBABs), the borneol derivative structure and grafted pyridine-triphenylborane (PTPB) as antifouling groups were prepared by radical polymerization. PBABs showed high antibacterial rates for Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) of up to 95.1% and 81.1%, respectively, confirming superior antibacterial adhesion propertys. More importantly, PBABs effectively reduced the expression of mussel adhesion protein, indicating superior antifouling propertys, resulting from the synergistic effect of multiple antifouling functional groups on the material's surface. Therefore, the PBABs have been evaluated as noncytotoxic, low-cost, easily synthesized, and mass-produced, which demonstrates their great potential for actual marine applications.

MOF-derived electrochemical catalyst Cu-N/C for the enhancement of amperometric oxygen detection.

Electrochemical sensors using ionic liquids as electrolytes for oxygen detection are now getting more and more attention. Recently, an ionic liquid combined with an electrochemically active catalyst system has become popular for boosting the sensing performance of oxygen sensors. In this work, the imidazolyl-based ionic liquid 1-butyl-2,3-dimethylimidazole bis((trifluoromethyl)sulfonyl)imide [Bmmim][TFSI] is first prepared by a facile two-step method. Subsequently, a transition metal and N-codoped porous carbon oxygen reduction electrochemical catalyst Cu-N/C is synthesized by calcining the Cu-doped ZIF-8 precursor and then blending it in different ratios with the ionic liquid [Bmmim][TFSI] as composite electrolytes for oxygen detection. The composite electrolyte Cu-N/C/[Bmmim][TFSI] exhibits increased responses in cyclic voltammetry (CV) and chronoamperometry (CA) relative to that of the pure ionic liquid. Furthermore, the CV and CA data show that 6% Cu-N/C/[Bmmim][TFSI] has the optimum oxygen sensing response with an enhanced reduction peak current, a sensitivity of 0.1678 µA/[% O2] and a good linear fitting coefficient of 0.9991. In conclusion, the results confirm the success of using Cu-N/C as an electrochemical catalyst composed of the Cu-N/C/[Bmmim][TFSI] electrolyte for improving the responsivity, stability and sensitivity towards a wide range of oxygen concentrations.

Ultra-high flexibility amidoximated ethylene acrylic acid copolymer film synthesized by the mixed melting method for uranium adsorption from simulated seawater.

If U(VI) in seawater (unconventional uranium resource) can be extracted efficiently, it can provide important supplies and guarantees for the stable development of nuclear power. In this study, a mixing melting method without condensation agent was proposed to prepare ultra-high flexibility and different proportions DAMN modified EAA resin film (EAA-DAMN) through the condensation reaction between -COOH and -NH2 and the uniform mixing of liquid EAA and DAMN. In addition, the dense film structure and -CN of EAA-DAMN were transformed into multiple pores structure and amidoxime groups of the amidoximated EAA (AO-EAA) by amidoxime reaction. The AO-EAA-3 showed the most excellent adsorption performance (qe=146.40 mg g-1) at pH = 5, which was 2.33 times that of EAA. Moreover, a hypothesis was proposed for the first time that -NH2 in the material could combine with H+ ionized by water to form -NH3+, and then adsorbed NO3- in the solution through electrostatic attraction, and O element from NO3- adsorbed on the surface and N-O from amidoxime groups of material as the adsorption active sites performed coordination with U(VI), thereby improving the adsorption performance of AO-EAA.

Constructing three-dimensional network C, O Co-doped nitrogen-deficient carbon nitride regulated by acrylic fluoroboron overall marine antifouling.

To deal with unwanted biofouling adsorption, which impacts the economy and the environment, significant research has been devoted to composite systems involving a photocatalyst combined with self-renewal resin to provide synergistic antifouling. Here, photocatalyst based on three-dimensional (3D) network of carbon-oxygen-doped nitrogen-deficient carbon nitride and acrylic fluoroboron polymer as a system was successfully synthesized. 3D networks carbon nitride with carbon-oxygen dopants and nitrogen defects were prepared as skeletons, which effectively support and regulate the hydrolysis rate of the polymer. These composite systems exhibits excellent diatom anti-adhesion performance and high antibacterial rates for Escherichia coli and Staphylococcus aureus of up to 91.87% and 88.52%, respectively. In addition, self-cleaning function of the composite system are proved by and higher efficiency of chemical oxygen demand (COD) removal owing to efficient charge-carrier separation and transfer within the 3D network carbon nitride network. The great potential applications of this strategy demonstrated in marine engineering in the future.

Bioinspired Durable Antibacterial and Antifouling Coatings Based on Borneol Fluorinated Polymers: Demonstrating Direct Evidence of Antiadhesion.

Substituting natural products for traditional poison-killing antifouling agents is an efficient and promising method to alleviate the increasingly serious ecological crisis and aggravate the loss due to marine biofouling. Herein, the successful synthesis of poly(methyl methacrylate-co-ethyl acrylate-co-hexafluorobutyl methacrylate-co-isobornyl methacrylate) copolymer (PBAF) with borneol monomers and fluorine by a free radical polymerization method is reported. The PBA0.09F coating exhibits outstanding antibacterial and antifouling activity, achieving 98.2% and 92.3% resistance to Escherichia coli and Staphylococcus aureus, respectively, and the number of Halamphora sp. adhesion is only 26 (0.1645 mm2) in 24 h. This remarkable antibacterial and antifouling performance is attributed to the incorporation of fluorine components into the copolymer, which induces a low surface energy and hydrophobicity and the complex molecular structure of the natural nontoxic antifouling agent borneol. In addition, the results showed that the contents of the adhesion-related proteins mfp-3, mfp-5, and mfp-6 were significantly reduced, which proved that natural substances affect the secretion of biological proteins. Importantly, the PBAF coating exhibits excellent environmental friendliness and long-term stability. The antifouling mechanism is clarified, and an effective guide for an environmentally friendly antifouling coating design is proposed.

Ultra-high mechanical property and multi-layer porous structure of amidoximation ethylene-acrylic acid copolymer balls for efficient and selective uranium adsorption from radioactive wastewater.

Adsorption uranium [U(VI)] from U-containing radioactive wastewater (URW) is a critical strategy for solving the resource shortage and environmental pollution in pace with the sustainable development of nuclear energy. However, the URW universally exhibits acidity and contains co-existing metal ions with high concentration. Herein, the amidoximation ethylene-acrylic acid copolymer balls (EAA-AO) with aciduric and super-high mechanical property were successfully synthesized through grafting diaminomaleonitrile and further treatment of amidoximation. Significantly, the mechanical properties of EAA-AO were not affected by the grafting process and maintained super-high mechanical properties. Furthermore, the -NH2 and unreacted -CN groups in diaminomaleonitrile adjusted the pKa to make the optimal pH be 4. In addition, the microstructure of EAA-AO was transformed from the original dense to multi-layer porous structure, which promoted the mass transfer process and the contact between uranyl ions (UO22+) and internal adsorption active sites. The adsorption capacity of EAA-AO was about 1.78 times that of EAA at pH = 4, and the adsorption capacity for U(VI) was about 8.17 times that of Ba2+ with the second highest adsorption capacity. Therefore, the EAA-AO exhibited ultra-high adsorption performance (qe = 3.196 mg g-1) in the artificial radioactive wastewater, laying a good foundation for subsequent large-scale industrial adsorption of U(VI) in nuclear industrial wastewater.

Mussel-inspired anti-biofouling and robust hybrid nanocomposite hydrogel for uranium extraction from seawater.

A major challenge of uranium extraction from seawater (UES) is to effectively block the biofouling without destroying the ecological balance, especially prevent the attachment of macroalgae on the surface of the adsorbent. Herein, a robust montmorillonite-polydopamine/polyacrylamide nanocomposite hydrogel is reported by a two-step method, including PDA intercalation MMT and further free radical polymerization with AM monomers. The interpenetrating structure of hydrogel lead to high water permeability with the swelling ratio of 51, which could fully facilitate the internal accessible sites exposure and increase the uranium diffusion. As a result, a high adsorption capacity of 44 mg g-1 was achieved in lab-scale dynamic adsorption. Most importantly, the prepared anti-biofouling hydrogel adsorbents display excellent anti-adhesion ability towards Nitzschia after 8 days contact. The adsorption capacity of uranium can reach 2130 µg g-1 in algae-contained simulated seawater. This hydrogel also exhibited a long service life of acceptable mechanical strength and adsorption capacity after at least 6 adsorption-desorption cycles. This new anti-biofouling nanocomposite hydrogel shows great potential as a new generation adsorbent for UES.

Superhydrophobic nanoporous polymer-modified sponge for in situ oil/water separation.

Developing an efficient and environmentally friendly strategy for oil-water separation is extremely important for practical application. In this study, a superhydrophobic and superoleophilic melamine sponge loaded with cross-linked and swellable polydivinylbenzene was successfully fabricated by a facile and effective one-step impregnation-curing method with adhesion of polydimethylsiloxane. The prepared sponge not only exhibited high oil absorption capacity, but it also enabled rapid oil collection in situ, which could be extended to practical application. Moreover, the modified superhydrophobic sponge showed excellent mechanical resistance and chemical stability. The surface morphology and chemical composition were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. This material has great development potential for large-scale oil spill clean-up and chemical spill accidents.

In Situ Anchoring of Pyrrhotite on Graphitic Carbon Nitride Nanosheet for Efficient Immobilization of Uranium.

Enrichment of UVI is an urgent project for nuclear energy development. Herein, magnetic graphitic carbon nitride nanosheets were successfully prepared by in situ anchoring of pyrrhotite (Fe7 S8 ) on the graphitic carbon nitride nanosheet (CNNS), which were used for capturing UVI . The structural characterizations of Fe7 S8 /CNNS-1 indicated that the CNNS could prevent the aggregation of Fe7 S8 and the saturation magnetization was 4.69 emu g-1 , which meant that it was easy to separate the adsorbent from the solution. Adsorption experiments were performed to investigate the sorption properties. The results disclosed that the sorption data conformed to the Langmuir isotherm model with the maximum adsorption capacity of 572.78 mg g-1 at 298 K. The results of X-ray photoelectron spectroscopy (XPS) demonstrated that the main adsorption mechanism are as follows: UVI is adsorbed on the surface of Fe7 S8 /CNNS-1 through surface complexation initially, then it was reduced to insoluble UIV . Thereby, this work provided an efficient and easy to handle sorbent material for extraction of UVI .

Rapid and efficient uranium(VI) capture by phytic acid/polyaniline/FeOOH composites.

Uranium plays an indispensable role in nuclear energy, but there are limited land resources to meet the ever growing demand; therefore, a need exists to develop efficient materials for capturing uranium from water. Herein, we synthesize a promising adsorbent of phytic acid/polyaniline/FeOOH composites (PA/PANI/FeOOH) by oxidative polymerization. Phytic acid, acting asa gelator and dopant, plays an important role in the formation of polyaniline (PANI). The PA/PANI/FeOOH exhibites high adsorption capacity (qm=555.8mgg-1, T=298K), rapid adsorption rate (within 5min), excellent selectivity and cyclic stability. In addition, the results show that the adsorption isotherm is well fitted to the Langmuir isotherm model, and the adsorption kinetics agree with a pseudo-second order model. XPS analysis indicates that the removal of uranium is mainly attributed to abundant amine and imine groups on the surface of PA/PANI/FeOOH. Importantly, the removal of uranium from low concentrations of simulated seawater is highly efficient with a removal rate exceeding 92%. From our study, superior adsorption capacities, along with a low-cost, environmentally friendly and facile synthesis, reveal PA/PANI/FeOOH asa promising material for uranium capture.

Efficient removal of uranium(vi) from simulated seawater using amidoximated polyacrylonitrile/FeOOH composites.

The ability to recover uranium, an important nuclear fuel, from seawater provides the potential for long-term sustainable fuel supply for nuclear energy. In this work, novel amidoximated polyacrylonitrile/FeOOH (FeOOH-APAN) composites were synthesized and characterized by CHN analysis, Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), N2 adsorption-desorption, and X-ray photoelectron spectroscopy (XPS). In batch adsorption experiments, a variety of parameters were investigated in detail. The FeOOH-APAN composites exhibit high adsorption capacities (qL = 980.39 mg g-1, T = 298 K), superior to many other materials. In addition, they possess large Kd values (>104 mL g-1 at 25-400 mg L-1 U concentration), high removal rates (∼95% at 25-300 mg L-1, and ∼90% for ppb level simulated seawater), excellent selectivity and rapid capturing rates for uranium. XPS analysis shows that the removal of uranium is mainly related to amidoxime groups, involving the interaction with oxime oxygen and oxime nitrogen. In this paper, a more dominant binding mode is proposed, namely η2 coordination.

Fabrication of ZIF-8@SiO2 Micro/Nano Hierarchical Superhydrophobic Surface on AZ31 Magnesium Alloy with Impressive Corrosion Resistance and Abrasion Resistance.

Superhydrophobic coatings are highly promising for protecting material surfaces and for wide applications. In this study, superhydrophobic composites, comprising a rhombic-dodecahedral zeolitic imidazolate framework (ZIF-8@SiO2), have been manufactured onto AZ31 magnesium alloy via chemical etching and dip-coating methods to enhance stability and corrosion resistance. Herein, we report on a simple strategy to modify hydrophobic hexadecyltrimethoxysilan (HDTMS) on ZIF-8@SiO2 to significantly improve the property of repelling water. We show that various liquids can be stable on its surface and maintain a contact angle higher than 150°. The morphologies and chemical composition were characterized by means of scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FI-IR). In addition, the anticorrosion and antiattrition properties of the film were assessed by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization and HT, respectively. Such a coating shows promising potential as a material for large-scale fabrication.

[Diagnostic value and influencing factors for amplitude-integrated EEG in brain injury in preterm infants].

OBJECTIVE: To study the diagnostic value and influencing factors for amplitude-integrated EEG (aEEG) in brain injury in preterm infants. METHODS: One hundred and sixteen preterm infants with a gestational age (GA) between 27 weeks and 36(+6) weeks were enrolled as subjects. The aEEG scores of all preterm infants were obtained within 6 hours after birth. According to the diagnostic results, the 116 preterm infants were divided into two groups: brain injury (n=63) and non-brain injury (n=53). The risk factors for brain injury were evaluated using logistic regression analysis. According to the aEEG results, the 116 preterm infants were divided into two groups: normal aEEG (n=58) and abnormal aEEG (n=58). The influencing factors for aEEG results in preterm infants were determined using univariate analysis. RESULTS: The brain injury group had a significantly higher rate of abnormal aEEG than the non-brain injury group (83% vs 11%; P<0.05). The infants in the brain injury group from two different GA subgroups (27-33(+6) weeks and 34-36(+6) weeks) had significantly lower aEEG scores than the non-brain injury group from corresponding GA subgroups (P<0.01). Logistic regression analysis showed that low GA (<32 weeks), low birth weight (<1 500 g), abnormal placenta, fetal membranes, and umbilical cord, and hypertension during pregnancy were high-risk factors for brain injury (P<0.05). There were significant differences in GA, birth weight, abnormal placenta, fetal membranes, and umbilical cord, and hypertension during pregnancy between the normal and abnormal aEEG groups (P<0.05). CONCLUSIONS: The risk factors for brain injury are consistent with the influencing factors for aEEG results in preterm infants, suggesting that aEEG contributes to the early diagnosis of brain injury.