Long-term Stability Research Articles

Ag Nanoparticles Modified Sea Urchin-like W18O49 Microstructures for Sensitive Surface Enhanced Raman Spectroscopy Detection

Surface-enhanced Raman scattering (SERS) has gained significant attention in various fields, including biomedical diagnostics, environmental monitoring, and food safety. This technique offers many advantages such as label-free detection and the ability to detect analytes at low concentrations. In this study, we present a variety of tungsten oxide (W18O49) microstructures as solid SERS substrates using various solvents realized by a simple hydrothermal approach. Among them, the well-defined sea urchin-like W18O49 microstructures support greater light scattering and confinement to enhance the SERS signal when compared to other W18O49 structures. The surface of well-defined sea urchin-like W18O49 microstructures was then modified with uniformly distributed silver nanoparticles (Ag NPs). The combination of the unique morphology of the Ag and sea urchin-like W18O49 microstructures (W18O49@Ag) led to improved detection capabilities for analytes such as rhodamine 6G (R6G) and thiram molecules. The SERS enhancement factor (EF) of sea urchin-like W18O49@Ag microstructures was estimated to be as high as 1.53×106 with the lowest detectable concentrations of 1nM and 1μM for R6G and thiram, respectively. Thus, the well-defined sea urchin-like W18O49@Ag microstructures are excellent choice to replace the pure noble metal SERS substrates in the fields of rapid detection and trace analysis due to their high sensitivity, repeatability, and long-term stability.

Advancements in printed components for proton exchange membrane fuel cells: A comprehensive review

Proton Exchange Membranes (PEM) are a promising technology for fuel cells and electrolyzer cells, in line with societal goals for clean and sustainable fuel conversion and generation, respectively, in a vast field of applications. PEM fuel cell (PEMFC) technology has an important advantage for energy conversion applications, because it requires a lower operating temperature and is lighter and more compact than other technologies, which makes it ideal for portable and transportation applications. However, open issues remain to be addressed for PEMFC that hinder their widespread adoption, both on the technical side, such as too high operational temperature range, cell efficiency, and long-term stability, as well as on the industrial side with implementation issues, material and device component availability, and cost. PEM technology research usually focuses on the synthesis of novel materials such as non-noble metal catalysts and non-halogenated membranes. In parallel, developing high-throughput and cost-effective manufacturing methods for components, in particular Membrane Electrode Assembly (MEA), can also lift an important barrier to their mass production, thus contributing to the same goals and securing industrial provision. From this perspective, printing technologies such as spray coating, inkjet printing, and screen printing have emerged as promising approaches with the required precision and scalability. This review covers recent advancements and developments in advanced PEMFC technology manufacturing, with a focus on 2D printing methodologies to fabricate some or all of the MEA components. Leveraging these techniques as simplified large-area manufacturing methods for PEM technology can become a more viable and industrially attractive solution. This work presents a comparison study addressing the key progress indicators both in process and in characterization to build a working framework in which both scientists, engineers and manufacturers can collaborate toward the industrial implementation of this emergent field.

A facile and scalable fabrication procedure for PVDF-PDA/PEI/SiO2 hollow fiber composite ultrafiltration membranes: Integration of co-deposition and cross-linking

Polyvinylidene fluoride (PVDF) membranes, widely used for their stability, face limitations due to the hardly adjustable pore size in nanoscale and inherent hydrophobicity. To address this, we proposed a co-deposition method incorporating dopamine (DA), polyethyleneimine (PEI), and silicon dioxide (SiO2) nanoparticles with glutaraldehyde cross-linking for precise regulation of pore size and hydrophilicity in PVDF hollow fiber membranes. Notably, the pore diameter reduced from 119.0 ± 3.55 nm to 18.4 ± 0.36 nm, while the contact angle decreased from 107.7° to 40.9°. This simultaneous regulation led to a high-performance PDA/PEI/SiO2-PVDF hydrophilic ultrafiltration membrane with a rejection rate exceeding 99% for 20 nm nanoparticles in a long-term simulated separation experiment while achieving a significant protein permeability of 97% in BSA permeation experiments. Additionally, the membrane demonstrated exceptional long-term stability, offering a novel approach for tuning the performance of ultrafiltration/microfiltration membranes.

Synthesis of metal–organic framework ZIF-9-Mel and its application as an electrochemical modifier in Pb2+ detection

In this study, a selective electrochemical sensor was introduced for determination of lead ions based on a metal–organic framework (MOF)-melamine together with carbon black (CB) on the glassy carbon electrode (GCE). Herein, the zeolitic imidazolate framework-9-Mel (ZIF-9-Mel), which is a type of MOF, was synthesized and used as an electrode modifier. The interaction between Pb2+ and amine groups is conditioned by dative attachment, which causes the complexation of Pb2+-N through soft–soft interactions. To enhance the performance of the modified electrode, several parameters such as the pH of the buffer solution, the deposition potential, and the deposition time that affect response were optimized. Under optimized conditions (pH = 3, deposition time = 270 s, deposition potential = −0.7 V) the ZIF-9-Mel/CB/GCE sensor shows two linear ranges (0.5 nM–50 nM and 50 nM–1000 nM), low detection limit (0.16 nM), long-term stability, good repeatability and desirable reproducibility by differential pulse voltammetry (DPV) technique. To display the sensor ability for actual application, ZIF-9-Mel/CB/GCE was used for Pb2+ detection in lettuce and tomato samples with excellent results. According to the introduced method, MOFs are satisfactory materials for fabricating effective electrochemical sensors to detect Pb2+ ions simply and cost-effectively.

Reconstruction of Fe sacrifice protective layer enables highly effective CoP catalyst for hydrogen evolution reaction at high current density

Under the background of “Green hydrogen,” the method of hydrogen production through coupling water electrolysis with renewable energy has raised heightened demands for fundamental hydrogen evolution catalysts. Recently, CoP-based catalysts have attracted much attention due to their excellent HER activity. However, the self-reconfiguration behavior of CoP in actual operation seriously affects its long-term hydrogen evolution stability. Herein, an in-situ reconstructed Fe sacrificial protective layer is proposed to inhibit the complete conversion of CoP in alkaline HER process and improve the stability of CoP-based catalysts. Through this sacrificial strategy, nearly 80 % of CoP is retained, forming a new Co(OH)2/COP as the active interface of HER. As result, the catalyst can maintain hydrogen evolution at high current density for more than 10 days, and show excellent dynamic response in start-stop experiment. In an Anionic Exchange Membrane electrode cell, a fully hydrolyzed water AEM cell needs only 1.9 V to drive 1 A cm−2 current density.

Encapsulation and characterization of ω-3 medium- and long-chain triacylglycerols microencapsulated with different proteins as wall materials

In this study, ω-3 medium- and long-chain triacylglycerols (MLCTs) microcapsules with excellent performance were obtained using soy protein as the wall component to address the oxidation-related problems of MLCTs. Additionally, the effect of soy, whey, or pea proteins on microcapsules in terms of the changes in their structure and physicochemical properties was investigated. The results showed that the small particle size, low PDI (polydispersity index) and zeta potential, fast adsorption rate, and low interfacial tension of these protein-based samples fabricated through the O/W template method were conducive to maintaining the integrity of microcapsules during spray-drying. The microcapsules, characterized by a spherical shape, exhibited superior encapsulation efficiency of 94.56%, surpassing the findings of previous investigations. Overall, these microcapsules exhibited long-term storage stability and low controllable release rates, which could be utilized as carriers for liposoluble actives.

Immobilization of Xylanase on ZnO nanoparticles obtained by green synthesis from Eupatorium cannabinum L. and its application in enrichment of fruit juices

Juice production is one of the main components of the nutritional food industry. Therefore, improving fruit juice quality and preventing the formation of negative by-products is important for human health. The role of environmentally friendly, safe and economically more affordable green nanocarriers in improving the quality of fruit juice is increasing day by day. For this purpose, zinc oxide nanoparticles (ZnONPs) were prepared from the aqueous extract of the Eupatorium cannabinum L. using the green synthesis method. After immobilization, structural and morphological characterizations of the prepared ZnONPs and xylanase (Xyl)@ZnONPs were carried out, which confirmed that both the synthesis of ZnONPs and the immobilization of Xyl enzyme on ZnONPs were successfully carried out. The biochemical parameters of Xyl@ZnONPs such as optimum pH and temperature, kinetic parameters, thermal stability, reusability, and storage stability were investigated and compared with free Xyl. After immobilization, the optimum pH of free Xyl shifted from 5.0 to an alkaline pH of 8.0, while no change in the optimum temperature (70 °C) was observed for both enzymes. While the activation energy of free Xyl was 5.56 kJ/mol, it was found to be 7.27 kJ/mol for Xyl@ZnONPs. Xyl@ZnONPs outperformed free Xyl due to its long-term storage stability and reusability. Moreover, Xyl@ZnONPs retained 50 % of its activity after 5 reuses and 87 % of its activity after 4 weeks of storage at room temperature. In addition, a decrease in Km value and an increase in Vmax value were observed after immobilization, which means the increased catalytic activity of the Xyl@ZnONPs. As a result of re-using Xyl@ZnONPs in orange juice for 6 cycles, clarification yield of 66.43 % was obtained under optimized conditions. Overall, this study prepared a suitable, environmentally friendly, and robust carrier support for Xyl immobilization and developed a biocatalyst that will provide high performance in the industrial field.

Role of aloe vera based nanofluids for cool thermal energy storage system: A comparative study

The present experimental investigation incorporates the preparation of aloe vera gel-based phase change nanofluid (NFPCM) for a cool thermal energy storage (CTES) system. Two sets of NFPCMs were produced by adding graphene nanoplatelets (GNP) in deionized water and aloe vera gel (0.20 wt%, 0.40 wt%, and 0.60 wt%). The zeta potential analysis shows that the NFPCM with aloe vera gel is more stable even after 60 days from the preparation (−44 mV). The thermal conductivity of NFPCMs was analyzed through the transient hot wire method and the enhancement of 42 %, and 37.5 % were measured in the ice phase for NFPCMs with aloe vera gel and DI water (0.60 wt%) respectively at the heat transfer fluid temperature of −15 °C. The NFPCMs with aloe vera gel show that the addition of GNP prepended the peak melting temperature from −16 °C to −10.5 °C, which is due to the quick formation of nuclei as compared to NFPCMs with DI water. Additionally, a slight reduction in the latent heat of only 7 % was observed. The charging characteristics of NFPCMs were studied in a single spherical capsule at −8 °C. The maximum reduction in total charging time of 25 % was recorded for the aloe vera gel-based NFPCM with a maximum concentration of GNP (0.60 wt%). The green synthesis of aloe vera gel-based NFPCM exhibited noteworthy enhancements in thermophysical properties. Additionally, it was observed that the long-term stability of the NFPCM was achieved by excluding surfactants during the preparation process. The incorporation of graphene nanoplatelets (GNP) into aloe vera gel as the foundational phase change material (PCM) facilitates the partial charging of the CTES system with a reduced energy input.

A Systematic Study of Methyl Carbodithioate Esters as Effective Gold Contact Groups for Single-Molecule Electronics.

There are several binding groups used within molecular electronics for anchoring molecules to metal electrodes (e.g., R-SMe, R-NH2, R-CS2-, R-S-). However, some anchoring groups that bind strongly to electrodes have poor/unknown stability, some have weak electrode coupling, while for some their binding motifs are not well defined. Further binding groups are required to aid molecular design and to achieve a suitable balance in performance across a range of properties. We present an in-depth investigation into the use of carbodithioate esters as contact groups for single-molecule conductance measurements, using scanning tunnelling microscopy break junction measurements (STM-BJ) and detailed surface spectroscopic analysis. We demonstrate that the methyl carbodithioate ester acts as an effective contact for gold electrodes in STM-BJ measurements. Surface enhanced Raman measurements demonstrate that the C=S functionality remains intact when adsorbed on to gold nanoparticles. A gold(I) complex was also synthesised showing a stable C=Sׄ→AuI interaction from the ester. Comparison with a benzyl thiomethyl ether demonstrates that the C=S moiety significantly contributes to charge transport in single-molecule junctions. The overall performance of the CS2Me group demonstrates it should be used more extensively and has strong potential for the fabrication of larger area devices with long-term stability.

Factors influencing charge transport at perovskite-charge transport layer interfaces: Current strategies, challenges and perspectives based on first-principles studies

Abstract The charge transport at the interface between the perovskite absorbing layer and the charge transport layer (CTL) has a major role in determining perovskite solar cell device efficiency and long-term stability. Hence, detailed operando characterization of the factors influencing the charge transport at the perovskite/CTL interface needs to be discussed. This perspective summarizes the recent studies involving the charge transport through perovskite and charge transport layer interfaces and an overview is provided on the recent advances in the fundamental understanding of how these interfaces influence the device performance. Based on recent reported articles, some of the crucial factors such as energy level alignment, defects, and non-radiative recombination are identified from an atomistic point of view as having influence on charge transport at the perovskite/CTL interface. Further, we share our perspective on calculating said factors influencing interfacial charge transport from the different approaches using density functional theory (DFT) and beyond.

Eliminating Voids and Residual PbI2 beneath a Perovskite Film via Buried Interface Modification for Efficient Solar Cells.

The commercialization process of perovskite solar cells (PSCs) is markedly restricted by the power conversion efficiency (PCE) and long-term stability. During fabrication and operation, the bottom interface of the organic-inorganic hybrid perovskite layer frequently exhibits voids and residual PbI2, while these defects inevitably act as recombination centers and degradation sites, affecting the efficiency and stability of the devices. Therefore, the degradation and nonradiative recombination originating from the buried interface should be thoroughly resolved. Here, we report a multifunctional passivator by introducing malonic dihydrazide as an interfacial chemical bridge between the electron transport layer and the perovskite (PVK) layer. MADH with hydrazine groups improves the surface affinity of SnO2 and provides nucleation sites for the growth of PVK, leading to the reduced residual PbI2 and the voids resulting from the inhomogeneous solvent volatilization at the bottom interface. Meanwhile, the hydrazine group and carbonyl group synergistically coordinate with Pb2+ to improve the crystal growth environment, reducing the number of Pb-related defects. Eventually, the PCE of the PSCs is significantly enhanced benefiting from the reduced interfacial defects and the increased carrier transport. Moreover, the reductive nature of hydrazide further inhibits I2 generation during long-term operation, and the device retains 90% of the initial PCE under a 1 sun continuous illumination exposure of 700 h.

Amine-Functionalized Metal-Free Nanocarbon to Boost Selective CO2 Electroreduction to CO in a Flow Cell.

Highly efficient electrochemical CO2-to-CO conversion is a promising approach for achieving carbon neutrality. While nonmetallic carbon electrocatalysts have shown potential for CO2-to-CO utilization in H-type cells, achieving efficient conversion in flow cells at an industrial scale remains challenging. In this study, we present a cost-effective synthesis strategy for preparing ultrathin 2D carbon nanosheet catalysts through simple amine functionalization. The optimized catalyst, NCNs-2.5, demonstrates exceptional CO selectivity with a maximum Faradaic efficiency of 98% and achieves a high current density of 55 mA cm-2 in a flow cell. Furthermore, the catalyst exhibits excellent long-term stability, operating continuously for 50 h while maintaining a CO selectivity above 90%. The superior catalytic activity of NCNs-2.5 is attributed to the presence of amine-N active sites within the carbon lattice structure. This work establishes a foundation for the rational design of cost-effective nonmetallic carbon catalysts as sustainable alternatives to metals in energy conversion systems.

Surface modification of biomedical titanium alloy for hard tissue repair and reconstruction

In biomedical applications, various materials are used, including metals and their alloys, polymers and ceramics. Among them, titanium (Ti) and titanium alloys are widely utilised in implant materials due to their excellent corrosion resistance and high mechanical strength. However, despite these advantages, titanium is biologically inert and does not integrate well with human cells. Therefore, surface modification of titanium implants plays a crucial role in determining the rate of osseointegration and the overall success of the implants. The primary objective of this review is to provide a detailed introduction to surface modification technologies for titanium alloy implants. The aim is to enhance the biological activity, wear resistance, corrosion resistance and antibacterial properties and reduce the release of ions from the implants. By modifying the surface of titanium implants, it is possible to create a more favourable environment for cell adhesion, proliferation and differentiation. Various techniques, such as physical methods (e.g. sandblasting, acid etching) and chemical methods (e.g. surface oxidation, plasma treatment) can be employed to modify the surface properties of titanium implants. These surface modification techniques can enhance the interaction between the implant and the surrounding biological environment, promoting osseointegration and improving the long-term stability of the implant. Additionally, surface modifications can help reduce the release of potentially harmful ions from the implant, minimise bacterial adhesion and improve the overall biocompatibility of the implant. In conclusion, surface modification of titanium alloy implants is a critical aspect of biomedical engineering. By improving the biocompatibility of titanium implants, these modifications contribute to the success and longevity of implants used in hard tissue repair and reconstruction.

Boosting Urea-Assisted Natural Seawater Electrolysis in 3D Leaf-Like Metal-Organic Framework Nanosheet Arrays Using Metal Node Engineering.

Metal node engineering, which can optimize the electronic structure and modulate the composition of poor electrically conductive metal-organic frameworks, is of great interest for electrochemical natural seawater splitting. However, the mechanism underlying the influence of mixed-metal nodes on electrocatalytic activities is still ambiguous. Herein, a strategic design is comprehensively demonstrated in which mixed Ni and Co metal redox-active centers are uniformly distributed within NH2-Fe-MIL-101 to obtain a synergistic effect for the overall enhancement of electrocatalytic activities. Three-dimensional mixed metallic MOF nanosheet arrays, consisting of three different metal nodes, were in situ grown on Ni foam as a highly active and stable bifunctional catalyst for urea-assisted natural seawater splitting. A well-defined NH2-NiCoFe-MIL-101 reaches 1.5 A cm-2 at 360 mV for the oxygen evolution reaction (OER) and 0.6 A cm-2 at 295 mV for the hydrogen evolution reaction (HER) in freshwater, substantially higher than its bimetallic and monometallic counterparts. Moreover, the bifunctional NH2-NiCoFe-MIL-101 electrode exhibits eminent catalytic activity and stability in natural seawater-based electrolytes. Impressively, the two-electrode urea-assisted alkaline natural seawater electrolysis cell based on NH2-NiCoFe-MIL-101 needs only 1.56 mV to yield 100 mA cm-2, much lower than 1.78 V for alkaline natural seawater electrolysis cells and exhibits superior long-term stability at a current density of 80 mA cm-2 for 80 h.

Comprehensive calibration and laboratory validation of a Micro Electromechanical System sensor–based flexible inclinometer

Abstract Real-time monitoring of slopes, tunnels, and dams is important for ensuring the long-term stability and reliability of such structures. Despite the successes of current technologies in many applications, a gap still exists in certain areas such as precision in steep slopes and complex soil conditions. This study has designed a flexible inclinometer based on an array of Micro Electromechanical System (MEMS) sensors to enhance the accuracy and flexibility of existing monitoring techniques. The inclination angle of each flexible inclinometer measurement unit was measured to monitor the horizontal or vertical displacement of the target structural body. We used the Levenberg–Marquardt (LM) algorithm for optimizing the MEMS sensors based calibration and designed multiple experiments to test the accuracy of the proposed method. Experimental results show that the calibrated flexible inclinometer measurement unit has an inclination angle of less than 0.04° and the accuracy of the flexible inclinometer lies within ±0.4 mm in the horizontal attitude and 1.6 mm in the vertical attitude. Our research has developed a novel tool for geotechnical engineering monitoring that can aid in increasing the precision of real-time assessment and prediction of structural stability.

Critical Review of Cu-Based Hole Transport Materials for Perovskite Solar Cells: From Theoretical Insights to Experimental Validation.

Despite the remarkable efficiency of perovskite solar cells (PSCs), long-term stability remains the primary barrier to their commercialization. The prospect of enhancing stability by substituting organic transport layers with suitable inorganic compounds, particularly Cu-based inorganic hole-transport materials (HTMs), holds promise due to their high valence band maximum (VBM) aligning with perovskite characteristics. This review assesses the advantages and disadvantages of these five types of Cu-based HTMs. Although Cu-based binary oxides and chalcogenides face narrow bandgap issues, the "chemical modulation of the valence band" (CMVB) strategy has successfully broadened the bandgap for Cu-based ternary oxides and chalcogenides. However, Cu-based ternary oxides encounter challenges with low mobility, and Cu-based ternary chalcogenides face mismatches in VBM alignment with perovskites. Cu-based binary halides, especially CuI, exhibit excellent properties such as wider bandgaps, high mobility, and defect tolerance, but their stability remains a concern. These limitations of single anion compounds are insightfully discussed, offering solutions from the perspective of practical application. Future research can focus on Cu-based composite anion compounds, which merge the advantages of single anion compounds. Additionally, mixed-cation chalcogenides such as CuxM1-xS enable the customization of HTM properties by selecting and adjusting the proportions of cation M. This article is protected by copyright. All rights reserved.

Determination of Trace Cd(II) in Water and Cosmetics based on Au/GO/CuO Nanocomposite Functionalized Electrochemical Sensor

Abstract Cadmium (Cd(II)) is highly toxic to environmental, and while many approaches have been developed to measure cumulative Cd(II) concentration over time, online monitoring of spatiotemporal changes remains challenging. To address this, an electrochemical sensor for determination of ultra-trace Cd(II) was developed, based on gold/graphene oxide/copper oxide (Au/GO/CuO) nanomaterials modifying glassy carbon electrode. CuO nanoparticles were prepared by a green synthesis method using plant extract, and the Au nanoparticles were deposited on the GO/CuO nanosubstrates by an in-situ electrochemical method. The prepared nanocomposites were characterized by field-emission scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The CuO nanoparticles are layered flower-like with an average particle size of 200-500 nm. Au/GO/CuO nanocomposites with high specific surface area and excellent electronic transmission capability enhanced the electrochemical signal of the sensor. Owing to the synergistic effect of Au/GO/CuO, the sensor exhibited good performance to Cd(II) in the ultra-wide range of 5×10-11 - 5×10-7 M with a detection limit of 2×10-11 M. The sensor was successfully quantified for determining Cd(II) with desirable recovery, displaying outstanding long-term stability, high sensitivity, and reproducibility. After validating its accuracy, this sensor was successfully used for detection of Cd (II) in water and cosmetic samples.

Engineering a high-performance W-doped Sr0.9Fe0.67Ti0.3Co0.03O3-δ hydrogen electrode for Solid Oxide Electrolysis Cells (SOECs)

Traditionally, Ni-based cermet fuel electrodes have been extensively utilized in Solid Oxide Electrolysis Cells (SOECs) for their excellent conductivity and catalytic properties. However, the development of alternative materials has gained attraction due to concerns over Ni's susceptibility to carbon deposition and long-term stability issues. To overcome this issue, we designed Sr0.9Fe0.67Ti0.30Co0.07O3-δ (SFTC) and W-doped SFTC (SFTCW) via the sol-gel method and thoroughly characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TG-DSC), and electrochemical tests. The results reveal that the incorporation of W enhances the stability of the electrode material under both oxidizing and reducing conditions, with no impurity phases detected. Furthermore, W doping promotes the precipitation of Co–Fe alloy, preserves the original structure, and facilitates the creation of oxygen vacancies within the material. In a reducing atmosphere containing 40 % H2O, SFTCW demonstrates superior electrolysis performance at an electrolysis voltage of 1.8 V, exhibiting a remarkable improvement of approx. 35 % compared to the SFTC sample. During a 100 h long-term stability test, the current density of SFTCW increased from -240 mA cm–2 to -270 mA cm–2, attributed to the enhanced hydrogen oxidation activity and increased reactive sites resulting from W doping, thereby enhancing its long-term stability. This work provides a feasible scheme for the selection and construction of hydrogen electrodes for electrolytic water.

Case Report: Double Pectus Up in severe pectus excavatum, the new frontier of modified taulinoplasty

IntroductionPectus excavatum, also known as “sunken chest” or “funnel chest,” is a congenital condition where the sternum caves inward, creating a noticeable depression in the chest. This deformity can range from mild to severe cases, and can affect appearance and lung and heart function. Treatment options vary depending on the severity of the condition and associated symptoms. A case study was conducted on three patients suffering from severe forms of pectus excavatum using modified taulinoplasty with two Pectus Up bars.Case descriptionThe patients were males, with an age of 15 years. Preoperatively, they underwent spirometry, an echocardiogram, and allergy tests. The procedure involved inserting two Pectus Up bars into the chest wall at the major sternal defect, allowing the implant to remain completely invisible. The procedure involved placing the sternal plate at the deepest point and anchored to the sternum with five self-tapping screws. The chest plate was then fixed to the bar using two screws.DiscussionThe use of Pectus Up was first reported in 2016 and has been a subject of scientific discussion and research. The double Pectus Up technique offers improved correction, increased stability, and reduced complications. However, it also presents challenges such as increased technical complexity and potential for prolonged operative times. Patient outcomes showed promising results in terms of short-term correction and long-term stability. The use of a double bar technique in the modified Taulinoplasty procedure is a key area of ongoing clinical research and innovation in pectus excavatum repair. Further studies will be needed, including more institutions that use this technique to validate our initial experience.

Peroxymonosulfate activation by superparamagnetic mixed-valent Cu/N-(L-cysteine)-O-(carboxymethyl)chitosan/cobalt ferrate-rice hull hybrid nanocomposite for efficient degradation of naproxen: Synergetic adsorption-catalysis, kinetics, pathway, and relevant mechanism.

Naproxen (NPX) as an emerging anthropogenic contaminant was detected in many water sources, which can pose a serious threat to the environment and human health. Peroxymonosulfate (PMS) decomposed by Cu(I) has been considered an effective activation method to produce reactive species. However, this decontamination process is restricted by the slow transformation of Cu(II)/Cu(I) by PMS. Herein, new N-(L-cysteine/triazine)-O-(carboxymethyl)-chitosan/cobalt ferrate-rice hull hybrid biocomposite was constructed to anchor the mixed-valent Cu(I)-Cu (II) (CuI, II-CCCF) for removing pharmaceutical pollutants (i.e., naproxen, ciprofloxacin, tetracycline, levofloxacin, and paracetamol). The structural, morphological, and catalytic properties of the CuI,II-CCCF have been fully identified by a series of physicochemical characterizations. Results demonstrated that the multifunctional, hydrophilic character, and negative ζ-potential of the activator, accelerating the redox cycle of Cu(II)/Cu(I) with hydroxyl amine (HA). The negligible metal leaching, well-balanced thermodynamic-kinetic properties, and efficient adsorption-catalysis synergy are the main reasons for the significantly enhanced catalytic performance of CuI,II-CCCF in the removal of NPX (98.6 % at 7.0 min). The main active species in the catalytic degradation of NPX were identified (●OH > SO4●- > 1O2 > > O2●-) and consequently suggested a degradation path. It can be noted that these types of carbohydrate-based nanocomposite offer numerous advantages, encompassing simple preparation, excellent decontamination capabilities, and long-term stability.