Surface Area Research Articles

Techno-Economic Analysis of Solar PV Electricity Generation at the University of Environment and Sustainable Development in Ghana

The electricity indebtedness of Ghanaian schools is increasing due to the high cost of electricity in the country. As a result, the utility companies frequently disconnect the schools from the grid to force them to settle their debts. Meanwhile, the school can reduce its bills from rooftop solar PV systems, yet little attention is given. The study uses the University of Environment and Sustainable Development (UESD) as a case to assess the technical feasibility, economic viability, and potential benefits of implementing rooftop solar PV electricity in Ghanaian schools. Google Earth software was used to estimate the structure's rooftop surface areas to determine the potential energy harvest from a PV plant.In contrast, the economic analysis uses the net present value (NPV), internal rate of returns (IRR), discounted payback period (DPP) and profitability index (IP) to appraise the intended project. The results show that using rooftops of school structures can provide the needed electricity for local consumption and export excess to the grid for sales. The NPV, IRR, IP, and DPP recorded from the study are million GHS 15.15, 21%, 1.6 and 8 years, respectively. The findings highlight the potential of rooftop solar PV systems to meet educational institutions' electricity demand, exploring the possibility of exporting excess to the national grid for revenue (income generator), reducing operational costs, and contributing to a sustainable energy transition.

Trojan Microparticles : A Composite Nanoparticle Delivery System

Abstract: In recent years, microparticulate systems have drawn growing attention as a viable strategy for delivering cells, proteins, and medications to target areas. The Nanoparticles-in-Microparticles System (NiMS) is a drug delivery method that combines nano- and microparticles to deliver medications or genes to particular bodily regions with precision. A promising method for achieving dual or multiple functions inside a formulation is the development of nanoparticle-in-microparticle systems (NiMS). NiMS comprises a microparticle (M.P.) matrix and one or more nanoparticles (N.P.s). The N.P.s can be designed to provide specific functionality, such as targeted drug delivery or imaging, while the M.P. matrix can be tailored to provide sustained release or protect the N.P.s from degradation. NiMS offer several advantages over traditional formulations, including the ability to control release profiles and achieve site-specific delivery. By combining different types of N.P.s and M.P.s, it is possible to create formulations that release drugs at different rates or with different kinetics, allowing for tailored treatment regimens. Additionally, by lowering off-target effects and boosting efficacy, the site-specific targeting offered by NiMS can enhance the therapeutic index of medications. Microparticles are small, micron-sized particles that can be loaded with therapeutic agents and designed to deliver them to specific tissues in the body. The pharmaceutical sector is developing microparticulate delivery systems for oral, pulmonary, and cutaneous administration. For instance, a promising strategy for treating respiratory conditions, including asthma and chronic obstructive pulmonary disease, is the development of inhalable microparticles (COPD). Moreover, the use of microparticles for topical drug delivery is being studied, where they can be formulated into creams, gels, or patches for treating skin disorders. The composition of microparticles is crucial for successful tissue regeneration because the particles must be biocompatible and able to interact with the cells in the targeted tissue. In addition, the size and shape of the particles can affect their behavior and how they interact with cells. Chemical and biological sensors and devices, optical detectors, electronic components, and nanoscale production depend on nanostructures because they offer unique properties, such as increased surface area and enhanced reactivity, which can be exploited to create more efficient and effective devices.

MOFs materials as photocatalysts for CO2 reduction: Progress, challenges and perspectives

Photocatalytic reduction of carbon dioxide (CO2) presents a pivotal solution to address meteorological and ecological challenges. Currently, metal-organic frameworks (MOFs) with their crystalline porosity, adjustable structures, and diverse chemical functionalities have garnered significant attention in the realm of photocatalytic CO2 reduction. This review provides a brief introduction to CO2 reduction and MOF material and their applications in CO2 reduction. Then, it undertakes a comprehensive examination of MOFs, summarizing their key attributes, including porosity, large surface area, structural multifunctionalities, and responsiveness to visible light, along with an analysis of heterojunctions and their methods of preparation. Additionally, it elucidates the fundamental principle of photocatalysis and CO2 reduction, encompassing both half and overall reactions. Furthermore, the classification of MOF-based materials is explored, along with the proposed mechanism for CO2 reduction and an update on recent developments in this field. Finally, this review outlines the challenges and potential opportunities for utilizing MOFs in CO2 reduction, offering valuable insights to scholars seeking innovative approaches not only to enhance CO2 reduction but also to advance other photocatalytic processes.

Two-dimensional MXene Nanomaterials: Preparation, Structure Modulation and the Applications in Electrochemical Energy Storage.

MXenes have attracted intensive attention owing to their unique twodimensional (2D) layered structure, high specific surface area, excellent conductivity, superior surface hydrophilicity, and chemical stability. In recent years, selective etching of the A element layers from MAX phases by fluorine-containing etchants (HF, LiF-HCl, etc) is a common method to prepare multilayered MXene nanomaterials (NMs) with plentiful surface terminations. At present, many studies have been reported on the use of fluorine-free etchants (NaOH, ZnCl2, etc) to etch MAX phases. The properties of MXene NMs are dependent on their structures. The purpose of this review is to focus on a comprehensive and systematical survey on the preparation, structure modulation, and applications of MXene NMs in electrochemical energy storage devices, including supercapacitors, lithium-ion battery, sodium-ion battery, potassium-ion battery, and aluminum-ion battery. Extensive information related to the preparation and applications of 2D MXene NMs for electrochemical energy storage and their associated patents were collected. This review highlights the recently reported 2D MXene NMs which are used in supercapacitor and various metal ion. It is found that the preparation methods have great impacts on the layer spacing and surface terminations of MXenes, consequently affecting their performance. Hence, this paper summarizes the research progress of the preparation strategies, layer spacing and surface termination modulation of MXene NMs. The applications of 2D MXene NMs in electrochemical energy storage are outlined. The forward-looking challenges and prospects for the development of MXenes are also proposed.

Normal Contact Model of Fractal Surfaces Considering Friction and Asperity Interactions

Friction as well as asperity interactions have significant influence on the contact area and force of rough surfaces. In this work, a single-asperity, elastoplastic contact model, considering friction, is established by means of continuum mechanics and power-exponential functions. Then, the deformation of the asperity interactions is modeled by the displacement of the average line for asperity height. Using fractal theory, the actual deformation and contact stiffness of an asperity are derived, which take the friction and asperity interactions into account. Furthermore, the actual contact area and normal stiffness models for fractal surfaces are developed, accounting for friction and asperity interactions. The accuracy of the developed models is confirmed by using published experimental results. The developed models are closer to experimental results than the reported fractal contact models. Finally, the effects of the friction coefficient and surface morphology parameters on contact characteristics are discussed.

Molecular Mechanism for Regioselectivity of P450-BM3 Monooxygenase Towards Stearic Acid Hydroxylation

Hydroxy stearic acid is an important raw material for the synthesis of biobased materials, and the hydroxylation at different positions showed different properties. With the catalysis of P450-BM3 monooxygenase, (ω - 1)-Hydroxy stearic acid was generated, which is a precursor of macrocyclic musk. Experimental results have shown that the L188Q mutant can increase the yield of (ω - 1)-Hydroxy stearic acid by more than three times, but the reason and underlying molecular mechanism are still unclear. In this study, molecular dynamics (MD) simulations were conducted to study the structural characteristics of the P450-BM3 wild type and its three mutants (F87V, L188Q, and F87V-L188Q) in combination with stearic acid. The MD simulation results showed significant changes in the interactions between the three mutants and the carboxyl- and terminal-end of stearic acid. The results of the Molecular mechanics-Poisson-Boltzmann surface area (MMPBSA) binding free energies indicated that the L188Q mutant showed the most stable binding with the stearic acid. Finally, the H-abstraction free energy barriers of L188Q and wild type systems were calculated to study the regioselectivity, and the results indicated that the L188Q mutant shown a significant advantage in the hydroxylation of stearic acid at the ω - 1 position. Our research results not only explain molecular mechanism for regioselectivity of P450-BM3 towards stearic acid hydroxylation, but also provide some useful ideas for the synthesis of biobased materials from hydroxy fatty acids.

Partial root-zone drying irrigation improves intrinsic water-use efficiency and maintains high photosynthesis by uncoupling stomatal and mesophyll conductance in cotton leaves.

Partial root-zone drying irrigation (PRD) can improve water-use efficiency (WUE) without reductions in photosynthesis; however, the mechanism by which this is attained is unclear. To amend that, PRD conditions were simulated by polyethylene glycol 6000 in a root-splitting system and the effects of PRD on cotton growth were studied. Results showed that PRD decreased stomatal conductance (gs) but increased mesophyll conductance (gm). Due to the contrasting effects on gs and gm, net photosynthetic rate (AN) remained unaffected, while the enhanced gm/gs ratio facilitated a larger intrinsic WUE. Further analyses indicated that PRD-induced reduction of gs was related to decreased stomatal size and stomatal pore area in adaxial and abaxial surface which was ascribed to lower pore length and width. PRD-induced variation of gm was ascribed to the reduced liquid-phase resistance, due to increases in chloroplast area facing to intercellular airspaces and the ratio of chloroplast surface area to total mesophyll cell area exposed to intercellular airspaces, as well as to decreases in the distance between cell wall and chloroplast, and between adjacent chloroplasts. The above results demonstrate that PRD, through alterations to stomatal and mesophyll structures, decoupled gs and gm responses, which ultimately increased intrinsic WUE and maintained AN.

RICH1 is a novel key suppressor of isoproterenol‑ or angiotensin II‑induced cardiomyocyte hypertrophy.

Cardiac hypertrophy is one of the key processes in the development of heart failure. Notably, small GTPases and GTPase‑activating proteins (GAPs) serve essential roles in cardiac hypertrophy. RhoGAP interacting with CIP4 homologs protein 1 (RICH1) is a RhoGAP that can regulate Cdc42/Rac1 and F‑actin dynamics. RICH1 is involved in cell proliferation and adhesion; however, to the best of our knowledge, its role in cardiac hypertrophy remains unknown. In the present study, the role of RICH1 in cardiomyocyte hypertrophy was assessed. Cell viability was analyzed using the Cell Counting Kit‑8 assay and cells surface area (CSA) was determined by cell fluorescence staining. Reverse transcription‑quantitative PCR and western blotting were used to assess the mRNA expression levels of hypertrophic marker genes, such as Nppa, Nppb and Myh7, and the protein expression levels of RICH1, respectively. RICH1 was shown to be downregulated in isoproterenol (ISO)‑ or angiotensin II (Ang II)‑treated H9c2 cells. Notably, overexpression of RICH1 attenuated the upregulation of hypertrophy‑related markers, such as Nppa, Nppb and Myh7, and the enlargement of CSA induced by ISO and Ang II. By contrast, the knockdown of RICH1 exacerbated these effects. These findings suggested that RICH1 may be a novel suppressor of ISO‑ or Ang II‑induced cardiomyocyte hypertrophy. The results of the present study will be beneficial to further studies assessing the role of RICH1 and its downstream molecules in inhibiting cardiac hypertrophy.

Current Expansion of Silver and Gold Nanomaterials towards Cancer Theranostics: Development of Therapeutics

Abstract: Nanomaterial-based therapeutics is an emerging tool for the treatment of numerous types of cancer. Various types of polymeric, lipid and inorganic nanoparticles (NPs) result in a wider series of applications in cancer diagnosis and therapeutics. The NPs properties are due to high surface area to volume ratio, surface plasmon resonance, absorption in the visible spectrum and light scattering. These unique characteristics of NPs arise due to their optical surface properties for conjugation/surface modification and smaller size. In cancer therapeutics, NPs based products are used as a biomarker for early detection/diagnosis of tumours, drug nano-conjugates for the delivery of chemotherapeutic drugs to the tumour-specific site, chemo-protective agents, etc. : Furthermore, other advantages of NPs are biocompatibility, lesser toxicity, enhanced permeability and retention effect, higher stability, and specific targeting with a selective accumulation of nano drugs in the tissue of the tumour. The selective targeting of NPs to tumour tissue is possible by adding surface-active targeting agents i.e., antibodies. The selective transport of drug NPs conjugates to the cancer cells is increased and extravagated due to permeable vasculature from endothelial cells gap while failing the transport of drug NPs conjugates in normal cells. This review emphasizes metallic NPs, including silver NPs (AgNPs) and gold NPs (AuNPs), which are extensively reconnoitered in various applications in cellular targeting, imaging, drug delivery, DNA-NPs conjugates for biosensor/point of care devices development, photothermal/photodynamic therapy, protein-protein interaction, etc. In addition, this review discussed different synthetic methods of AgNPs and AuNPs and characterization methods. Furthermore, it highlighted the different properties and applications of AgNPs and AuNPs in cancer theranostics.

Retentive strength of cement-retained implant-supported fixed dental prostheses according to different cement types and cementation protocols: An in vitro study.

To develop the most compatible cementation protocol for ensuring minimal residual cement and optimal retention of cement-retained implant-supported fixed dental prostheses. Thirty custom implant abutments and zirconia crowns with bilateral wings were prepared. Three cement types were used for cementation: non-eugenol resin cement (Premier Implant Cement; Group IC), dual-polymerizing self-adhesive resin cement (SmartCem 2; Group SC), and zinc oxide eugenol cement (Temp-Bond; Group TB) (n=30 per group). Three cementation methods were applied for each cement type and the samples were divided into subgroups: 1) cement was injected using a graduated syringe (IC-N, SC-N, and TB-N); 2) a cementation jig made with a silicone impression material and temporary resin material was used (IC-CJ, SC-CJ, and TB-CJ); 3) three dimensionally (3D) printed abutments were used as replicas for cementation (IC-3DP, SC-3DP, and TB-3DP). The amount of cement injected, surface area of the residual cement, and retentive strength were measured. Kruskal-Wallis and post-hoc Mann-Whitney tests were used for statistical analyses. Excess cement was not observed when cementation jig or 3D-printed replicas were used. For IC and SC subgroups, non-use of these auxiliary tools resulted in significantly higher amounts of injected cement. The retentive strength differed significantly among the IC subgroups, but not among the SC subgroups. The retentive strength of subgroups TB-N and TB-CJ was significantly higher than that of subgroup TB-3DP. To prolong the main purpose of each cement type, a cementation jig or 3D-printed replica is highly recommended regardless of the cement type. Int J Prosthodont 2023. doi: 10.11607/ijp.8344.

The Effect of Solvent on the Characteristics of FeBTC MOF as a Potential Heterogenous Catalyst Prepared via Green Mechanochemical Process

In this study, the synthesis of FeBTC (BTC = 1,3,5-benzenetricarboxylate) also known as MIL-100 (Fe) metal organic framework (MOF) has been carried out successfully using green mechanochemical method (neat grinding and liquid assisted grinding). The effect of solvent used in the synthesis was investigated for the first time to elucidate the physicochemical properties of FeBTC including crystal structure, thermal stability, pore size and specific surface area. The physicochemical properties of all FeBTC obtained in this study were compared to commercial FeBTC (Basolite F-300), characterized using powder X-Ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and nitrogen physisorption isotherms. All Fe-BTC MOF synthesized in this study showed improved textural properties compared to commercial Basolite F-300 such as higher crystallinity, higher surface area and larger pore size. It was found that the best synthesis method was by using the mixture of ethanol and water with equal volume ratio as solvent. The highest BET surface area of FeBTC synthesized using this method was 972 m2/g for FeBTC-EtOH/H2O. This value is 2.3 times higher than the surface area of commercial Basolite F-300 (418 m2/g). FeBTC with higher surface area is expected to have higher catalytic activity which makes this FeBTC an excellent candidate as a heterogenous catalyst for many reactions such as aldol condensation or esterification reaction. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

The Properties and Activity of TiO2-based Nanorods as an Anti-Fouling Agent and a Photocatalyst

The properties and activity of TiO2-based nanorods as an antifouling agent and a photocatalyst for the catalytic degradation of methylene blue (MB) have been investigated. A modification of TiO2 with SiO2 was first carried out to enlarge the surface area. In order to enhance the TiO­2 photo response to the visible light region, a further modification of TiO2-SiO2 (TS) composites with polyaniline (PANI) was also conducted. The nanorod TiO2 exhibited an anatase structure based on the diffraction patterns. The TEM images showed that some TiO2 molecules were attached around SiO2 with a random orientation. The TiO2-SiO2-PANI (TS-PANI) exhibited the largest specific surface area (SBET) of about 256.85 m2/g. The profile on the AFM images of the composites showed that the nano-roughness of the coatings was confirmed. The photocatalytic activity was evaluated through the decomposition of MB both on the powder and the coated composites. The photocatalytic activity on the coatings was verified due to further application as anti-fouling coatings involving photocatalytic mechanism. The decomposition of MB using TS-PANI powder and TS-PANI coating composites was 89.5% and 90.2 %, respectively, with the irradiation time on the coatings was 20 min longer. The anti-fouling activity through the photocatalytic mechanism and nano-roughness surface was confirmed by the inhibition of barnacle growth on the teakwood surface immersed for two months in the sea.

СТЕКЛОКЕРАМИЧЕСКИЕ ПОКРЫТИЯ НА ДЕНТАЛЬНЫХ ИМПЛАНТАТАХ С БАРЬЕРНЫМИ СВОЙСТВАМИ

Pateks — the technology of applying a biocompatible glass-ceramic coating based on silicon, carbon and nitrogen on dental implants by PECVD is developed by research and production company Plasmacentre and Pavlov University (St. Petersburg, Russia). Purpose of the research — to evaluate the success of optimization of the surface of doped titanium endosseous dental implants which may be achieved with our glass-ceramic barrier coating technology using physicochemical, cytological and spectrophotometric researches. The main task is to carry out a comparative assessment of the studies’ results between dental implants with and without Pateks glass-ceramic coating (doped with titanium alloy). Materials and methods. Titanium implants (grade 5) from BioMed were used in this research. Some of them were coated with Pateks according to our technology. A human lung fibroblast cells culture was used for the cytological study. Spectrophotometric studies were carried out on atomic absorption spectrophotometer and a atomic absorption spectrometer KVANT-Z.ETA (Russia). Findings. Pateks-coated implants demonstrate advantage in comparison with non-coated ones in certain physicochemical parameters such as decrease of defects’ area in the initial surface of titanium implants which is formed on the previous stages of surface shaping and processing, providing higher surface hydrophilicity, increasing of dielectric characteristics and higher pH value. Pateks coating is safe for fibroblast monolayers and does not inhibit respiratory processes in them. Applying of Pateks glass-ceramic coating with a thickness of 0.5 μm reduces the content of aluminum and vanadium ions in the model medium by almost 2 times and pro- vides a barrier that helps to reduce the negative biological effect of these ions on peri-implant tissues.

Catalytic Hydroconversion of Lauric Acid Over Poly(N-vinyl-2-pyrrolidone)-Coated Pd Nanoparticles on ZIF-8

A subclass of Metal-Organic Frameworks, Zeolitic Imidazole Frameworks-8 (ZIF-8) is known as an emerging material that has the characteristic of a large surface area, good thermal stability as well as a high porosity. Instead of having extraordinary properties, ZIF-8 consists of Lewis acid and Lewis base site on its Zn metals and 2-methylimidazole which are the important components for the catalyst. In this study, Pd-Poly(N-vinyl-2-pyrrolidone) coated on ZIF-8 (Pd-PVP@ZIF-8) was synthesized by mixed Pd-PVP solution and ZIF-8 precursors at room temperature. The Pd-PVP solution was varied from 10 to 50 ml to differentiate the Pd concentration in ZIF-8. As-synthesized 50 ml of Pd-PVP on ZIF-8 (50Pd-PVP@ZIF-8) showed catalytic activity in the conversion of 98.6% lauric acid to produce 78.2% of 1-dodecanol at optimum condition 320 °C for 6 h. The synergy between Pd-PVP as metal and ZIF-8 as metal support as well as high dispersion of Pd particles could enhance performance in the conversion of lauric acid. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Synthesis of Metal-Organic Framework (MOF) Cr-PTC-HIna for Heavy Metal Ion Adsorption

As an adsorbent material, Metal-Organic Framework (MOF) provides several advantages, such as large surface area and pore volume, as well as stability in aqueous systems both in acidic, basic, and neutral conditions. The research successfully made a metal organic framework (MOF) from chromium and perylene that was modulated by isonicotinic acid. This was done using three different methods: hydrothermal (Cr-PTC-HIna-HT), solvothermal (Cr-PTC-HIna-ST), and sonochemical (Cr-PTC-HIna-SC). The Cr-PTC-HIna-SC showed the greatest Pb2+ ion adsorption capacity. The optimum adsorption of Pb2+ ions occurred at 150 ppm Pb2+ ion concentration, pH 5, 90 minutes of contact time, and an adsorption capacity of 149.95 mg/g at 35 °C. The dominant adsorption isotherm model is the Langmuir isotherm model with R2 = 0.9867 and follows the pseudo-second-order. The selectivity test showed that Cr-PTC-HIna-SC MOF could adsorb more Cd2+ ions than Pb2+ ions, with 250 mg/g being the best amount.

Synthesize and Characterization of Pt-supported Co-ZIF for Catalytic Hydrocracking and Hydroisomerization of n-Hexadecane

Zeolitic Imidazole Frameworks (ZIFs) are prospective porous materials as catalyst support due to their relatively large surface area, and tunability in size, structure, and porosity. Recent studies have also shown that ZIF is the best candidate for various catalytic redox reactions such as the oxidation of benzyl aromatic hydrocarbons. In this study, the synthesized Pt catalyst supported on Co-ZIF was varied by the organic ligands: imidazole, benzimidazole, and 1-(3-aminopropyl) imidazole, then followed by impregnation of Pt precursor. The catalysts were characterized its physical and chemicals properties such as Fourier Transform Infrared (FTIR), X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Brunauer Emmet Teller (BET), Temperature-Programmed Desorption (NH3-TPD and CO2-TPD). The prepared catalysts were evaluated for catalytic hydrocracking and hydroisomerization of n-hexadecane in a 100 ml-batch reactor. GC-MS analysis presented that the Pt/ZIF catalyst with imidazole ligands has better performance than others. Hence, the optimization of n-Hexadecane conversion was carried out by the Pt/ZIF-imidazole catalyst varying the amount of metal loading, time and temperature reaction. The results showed that the reaction temperature of 350 ºC using 20 bar H2 for 4 h and the addition of 15 wt% Pt successfully achieved 90.77% conversion and produced the highest yield of isomers and alkanes, 4.04% and 35.75%, respectively. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Use of Sulfuric Acid-Impregnated Biochar Catalyst in Making of Biodiesel From Waste Cooking Oil Via Leaching Method

The biodiesel synthesis of waste cooking oil (WCO) over a impregnated biochar catalyst was systematically studied. This research aimed to prepare Biochar-based material that comes from coconut coir, activate it, and apply it as a catalyst to the esterification reaction of high-FFA waste cooking oil. Activation of the catalyst was done by impregnation H2SO4 solution in Biochar. The obtained catalyst was characterized by FTIR, XRF, XRD, surface area analyzer, and SEM-EDS. The esterification process was conducted by varying the catalyst weight (5, 7, and 10 wt%) and the reaction temperature (55 and 60 °C). The obtained liquid yields were characterized by GC-MS. The study found that the esterification process worked best with 10 wt% catalysts, a 1:76 mole ratio of oil to alcohol, and a reaction temperature of 60 °C. The waste cooking oil was successfully converted into biodiesel, reaching 84.50% of yield and 77.30% of purity (methyl ester content). Meanwhile, testing using national biodiesel standards with parameter limits of density, viscosity, iodine number, and acid number shows results that meet the requirements. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Efficient Atomically Dispersed Co/N-C Catalysts for Formic Acid Dehydrogenation and Transfer Hydrodeoxygenation of Vanillin.

Atomically dispersed catalysts have gained considerable attention due to their unique properties and high efficiency in various catalytic reactions. Herein, a series of Co/N-doped carbon (N-C) catalysts was prepared using a metal-lignin coordination strategy and employed in formic acid dehydrogenation (FAD) and hydrodeoxygenation (HDO) of vanillin. The atomically dispersed Co/N-C catalysts showed outstanding activity, acid resistance, and long-term stability in FAD. The improved activity and stability may be attributed to the high dispersion of Co species, increased surface area, and strong Co-N interactions. XPS and XAS characterization revealed the formation of Co-N3 centers, which are assumed to be the active sites. In addition, DFT calculations demonstrated that the adsorption of formic acid on single-atom Co was stronger than that on Co13 clusters, which may explain the high catalytic activity. The Co/N-C catalyst also showed promising performance in the transfer HDO of vanillin with formic acid, without any external additional molecular H2.

The Utilization of Metal-Organic Frameworks and Their Derivatives Composite in Supercapacitor Electrodes.

Up to now, the mainstream adoption of renewable energy has brought about substantial transformations in the electricity and energy sector. This shift has garnered considerable attention within the scientific community. Supercapacitors, known for their exceptional performance metrics like good charge/discharge capability, strong power density, as well as extended cycle longevity, have gained widespread traction across various sectors, including transportation and aviation. Metal-organic frameworks (MOFs) with unique traits including adaptable structure, highly customizable synthetic methods, and high specific surface area, have emerged as strong candidates for electrode materials. For enhancing the performance, MOFs are commonly compounded with other conducting materials to increase capacitance. This paper provides a detailed analysis of various common preparation strategies and characteristics of MOFs. It summarizes the recent application of MOFs and their derivatives as supercapacitor electrodes alongside other carbon materials, metal compounds, and conductive polymers. Additionally, the challenges encountered by MOFs in the realm of supercapacitor applications are thoroughly discussed. Compared to previous reviews, the content of this paper is more comprehensive, offering readers a deeper understanding of the diverse applications of MOFs. Furthermore, it provides valuable suggestions and guidance for future progress and development in the field of MOFs.

A Porphyrinic Metal-Organic Framework with Cooperative Adsorption Domains for PFAS Removal from Water.

The removal of toxic poly- and perfluoroalkyl substances (PFAS) as persistent pollutants from wastewater is imperative but challenging for water remediation. Many adsorbents including activated carbon, biochar, and clay minerals have been investigated for PFAS removal, but most of these materials are faced with high cost or/and low efficiency. The use of metal-organic frameworks (MOFs) as sorbents is attractive for efficient removal of PFAS due to their tailor-made structures and high surface areas. Herein, we synthesized, characterized a water stable Zr-based porphyrinic MOF (PCN-224) with cooperative adsorption domains, and demonstrated its excellent capture performance toward perfluorooctane sulfonate (PFOS), perfluorohexane sulfonate (PFHxS) and perfluorobutane sulfonate (PFBS). PCN-224 has maximum uptake capacities of 963, 517, and 395 mg g-1 for PFOS, PFHxS, and PFBS, respectively, which are much higher than that of granular activated carbon. Moreover, coexistent anions (Cl-, SO4 2-) and humic acid have negligible effects on PFOS adsorption. The excellent adsorption performance of PCN-224 toward PFOS is due to the orthogonal cationic channel pores with a diameter of 1.9 nm, the hydrophobic porphyrin units, and the Zr6 clusters with acidic sites. PCN-224 can be readily regenerated and reused. This work highlights the potential of MOFs with multiple adsorption domains for water remediation.