Enhancing corrosion resistance of mild steel in hydrochloric acid with Chiquita banana sap extract.

The corrosion of metals is still a huge challenge for various industries, and the pursuit of effective treatments ensures environmental sustainability. In this study, we utilized Chiquita banana sap-water extract (BSWE) to prevent mild steel from electrochemical corrosion in a 0.1 M HCl at room temperature. Corrosion resistance was assessed using various electrochemical methodologies, combining with surface characterization techniques. The results showed a high level of effectiveness when the corrosion current density decreased from 3292.67 µA cm-2 (for the sample immerged in the blank solution) to 187.33 µA cm-2 after 24 hours of immersion in the solution containing BSWE at a 2000 ppm concentration, equivalent to corrosion efficiency of 94.32%. Surface characterization revealed diminished corrosion on the inhibited steel surface due to the formation of a protective layer. X-ray photoelectron spectroscopy results demonstrated the presence of BSWE ingredients combining with iron oxides and hydroxides to form a smooth protective layer. Furthermore, theoretical calculations also indicated that the addition of BSWE can reduce steel surface damage when exposing to corrosive environment. The inhibitor based on banana sap extract can be referred to as a sustainable protective coating since it is biodegradable, abundantly available in banana plants and free of other harmful substances.

Enriched photocatalytic and photoelectrochemical activities of a 2D/0D g-C3N4/CeO2 nanostructure.

Sunlight-powered photocatalysts made from CeO2 nanosized particles and g-C3N4 nanostructures were produced through a thermal decomposition process with urea and cerium nitrate hexahydrate. The preparation of g-C3N4, CeO2, and a binary nanostructured g-C3N4/CeO2 photocatalyst was done through a facile thermal decomposition method. The structural properties were analyzed using powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy (XPS). Photocatalyst properties were characterized by using crystal violet (CV), a UV-Vis spectrophotometer, photocurrent and electron impedance spectroscopy (EIS). The structural and morphological analyses revealed that the g-C3N4/CeO2 nanostructures significantly enhanced the photoactivity for CV dye degradation under simulated sunlight, with a degradation rate of 94.5% after 105 min, compared to 82.5% for pure g-C3N4 and 45% for pure CeO2. This improvement was attributed to the noticeable visible light absorption and remarkable charge separation abilities of the nanostructures. Additionally, the g-C3N4/CeO2 nanostructures showed notable PEC performance under simulated sunlight. This study presents an easy and efficient method for producing g-C3N4 photocatalysts decorated with semiconductor materials and provides insights for designing nanostructures for photocatalytic and energy applications.

Pouch-Type Asymmetric Supercapacitor Based on Nickel-Cobalt Metal-Organic Framework.

Bimetal-organic frameworks (BMOFs) have attracted considerable attention as electrode materials for energy storage devices because of the precise control of their porous structure, surface area, and pore volume. BMOFs can promote multiple redox reactions because of the enhanced charge transfer between different metal ions. Therefore, the electroactivity of the electrodes can be significantly improved. Herein, we report a NiCo-MOF (NCMF) with a three-dimensional hierarchical nanorod-like structure prepared using a facile solvo-hydrothermal method. The as-prepared NCMF was used as the positive electrode in a hybrid pouch-type asymmetric supercapacitor device (HPASD) with a gel electrolyte (KOH+PVA) and activated carbon as the negative electrode. Because of the matchable potential windows and specific capacitances of the two electrodes, the assembled HPASD exhibits a specific capacitance of 161 F·g-1 at 0.5 A·g-1, an energy density of 50.3 Wh·kg-1 at a power density of 375 W·kg-1, and a cycling stability of 87.6% after 6000 cycles. The reported unique synthesis strategy is promising for producing high-energy-density electrode materials for supercapacitors.

Ternary nanocomposites of CdS/WO3/g-C3N4 for hydrogen production.

The sustainable rise in global warming and the consumption of fossil fuels considerably contribute to energy and environmental issues. To address these issues, semiconductor heterostructures can be used to generate clean energy sources as alternative energy sources and to reduce environmental impacts. Herein, we report the synthesis of a ternary semiconductor of the CdS/WO3/g-C3N4 (i.e. C-CNW) nanostructured composite for hydrogen production and dye degradation under visible-light irradiation. The structural properties of the prepared materials were studied using a series of investigational analyses. The 3C-CNW nanostructure photocatalyst exhibited faster malachite green (MG) dye photodegradation within 105 min and the highest hydrogen production rate is 868.23 µmol g-1 h-1 under visible light illumination. Moreover, the photocatalytic hydrogen production of the 3C-CNW nanostructure photocatalyst with various scavengers was analyzed. Its higher photocatalytic activity is ascribed to the Z-scheme mechanism, which induces rapid diffusion of photoinduced charges within the ternary photocatalyst with its optical bandgap. This proposed strategy is useful to improve photocatalysts that play a role in mitigating energy and environmental issues.

Role of SnO2 Nanoparticles for a Self-Forming Barrier Layer on a Mild Steel Surface in Hydrochloric Acid Medium Containing Piper betle Leaf Extract.

The self-formation of a porous organic thin-film via corrosion inhibitor supports wide applications of carbon steel in industry. Unfortunately, serious damages could be concentrated to the pinhole and/or pore locations in the porous organic film, resulting in the localized corrosion even when an optimal concentration of organic corrosion inhibitors is used. In this work, SnO2 nanoparticles are used for producing the more robust barrier layer via the self-migration of nanoparticles, resulting in a higher corrosion resistance, smooth and uniform protective layer, as well as the existence of SnO2 in the protective layer that could directly affect the high inhibition performance. Therefore, the work suggests a new way to make a more robust thin film that could extend the use of organic corrosion inhibitors.

Corrosion Inhibition of Mild Steel in Hydrochloric Acid Environments Containing Sonneratia caseolaris Leaf Extract.

Sonneratia caseolaris leaf extract was characterized for its mitigation of the electrochemical corrosion of steel in naturally aerated hydrochloric acid environments by electrochemical methods and surface analysis. The presence of S. caseolaris leaf extract (SCLE) in the hydrochloric acid medium ameliorated the corrosion resistance of steel via the adsorption of SCLE species to form a barrier layer. The improved inhibition effectiveness was demonstrated to be independent of the SCLE concentration and the corrosive environment. The highest inhibition performance of approximately 98% was reached for steel in a 1 M HCl medium containing 2500 ppm SCLE. The performance significantly decreased with a decrease in the HCl concentration from 1.00 to 0.01 M with the same SCLE concentration. In addition, severe corrosion occurred on the uninhibited steel surface but was significantly reduced on the inhibited steel surface. The analyzed results also indicated the existence of electronegative functional groups in SCLE, which could promote the adsorption process for the self-formation of the barrier layer on the steel surface. The work reported herein suggested a powerful strategy to mitigate electrochemical corrosion by adding an effective new inhibitor to achieve a green inhibitor system.

Onion-Ring-like Carbon and Nitrogen from ZIF-8 on TiO2/Fe2O3 Nanostructure for Overall Electrochemical Water Splitting.

The carbon and nitrogen derived from ZIF-8 embedded in TiO2/Fe2O3 (i.e., C,N-ZIF/TiFe) nanostructures exhibit superior electrocatalytic performance toward oxygen evolution reactions (OER), hydrogen evolution reactions (HER), and overall H2O splitting. The results showed that the C,N-ZIF/TiFe nanostructure was the best catalyst in comparison to ZIF/TiFe and TiFe nanostructures toward HER and OER. These results revealed that combining the highly active carbon and nitrogen from ZIF-8 with a TiO2/Fe2O3 semiconductor enriched the overall H2O splitting. A possible OER mechanism is attributed to some groups that support the surface active site of the catalyst and adsorbent intermediate species. Finally, this inexpensive electrocatalyst was synthesized without noble metals and showed superior electrocatalytic activity and great stability with the potential to achieve ground-breaking and novel applications in fuel cells.

Rationally engineered nanosensors: A novel strategy for the detection of heavy metal ions in the environment.

Heavy metal ions (HMIs) have been mainly originated from natural and anthropogenic agents. It has become one of biggest societal issues due to their recognised accumulative and toxic effects in the environment as well as biological media. Key measures are required to reduce the risks posed by toxic metal pollutants existing in the environment. The increased research activities of HMIs detection, and use of technologies based on electrochemical detection that combine with engineered nanomaterials, is a key promising and innovative strategy that can potentially confine heavy metal poisoning. Deep understanding of the characteristics of the physicochemical properties of nanomaterials is highly required. It is also important to interpret the parameters at the nano-bio interface level that merely affect cross-interactions between nanomaterials and HMIs. Therefore, the authors outlined the state-of-the-art techniques that used engineeringly developed nanomaterials to detect HMIs in the environment. The possible novel applications of extensive and relatively low-cost HMIs monitoring and detection are discussed on the basis of these strengths. Finally, it is concluded by providing gist on acquaintance with facts in the present-day scenario along with highlighting areas to explore the strategies to overcome the current limitations for practical applications is useful in further generations of nano-world.

Dual Interactions of Amphiphilic Gelatin Copolymer and Nanocurcumin Improving the Delivery Efficiency of the Nanogels.

Herein, a new process to manufacture multicore micelles nanoparticles reinforced with co-assembly via hydrophobic interaction and electrostatic interaction under the help of ultrasonication was developed. The precise co-assembly between negative/hydrophobic drug and positive charged amphiphilic copolymer based pluronic platform allows the formation of complex micelles structures as the multicore motif with predefined functions. In this study, curcumin was selected as a drug model while positively charged copolymer was based on a pluronic-conjugated gelatin with different hydrophobicity length of Pluronic F87 and Pluronic F127. Under impact of dual hydrophobic and electrostatic interactions, the nCur-encapsulated core-shell micelles formed ranging from 40 nm to 70 nm and 40-100 nm by transmission electron microscopy (TEM) and Dynamic Light Scattering (DLS), respectively. It is found that the structures emerged depended on the relative lengths of the hydrophobic blocks in pluronic. Regarding g2(τ) behavior from DLS measurement, the nanogels showed a high stability in spherical form. Surprisingly, the release profiles showed a sustainable behavior of Cur from this system for drug delivery approaches. In vitro study exhibited that nCur-encapsulated complex micelles increased inhibitory activity against cancer cells growth with IC50 is 4.02 ± 0.11 mg/L (10.92 ± 0.3 µM) which is higher than of free curcumin at 9.40 ± 0.17 mg/L (25.54 ± 0.18 µM). The results obtained can provide the new method to generate the hierarchical assembly of copolymers with incorporated loading with the same property.