Friendly Synthesis Research Articles

An efficient and environmental friendly synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione in aqueous hydrotropic medium

An efficient and environmental friendly synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione in aqueous hydrotropic medium

Facile and Environmentally Friendly Synthesis of Ga2O3/MFI Catalysts for Propane Dehydrogenation.

A GaOx-based catalyst is recognized as a promising catalyst for dehydrogenation of light alkanes. Conventionally, impregnation and calcination are necessary processes for the loading of GaOx. However, the incomplete impregnation of gallium salt solution would generate wastewater, and the calcination for the dissociation of gallium salt would release harmful gases, such as SOx, NOx, and HCl. Meanwhile, the high temperature results in an excessive energy cost and undesired GaOx particle aggregation. Here, we report a facile and environmentally friendly method for the synthesis of GaOx-based catalysts. The gallium salt solution was replaced directly with liquid gallium (LG). Through a simple physical mixing method at room temperature, uniform GaOx nanoparticles with diameters of around 3.5 nm were loaded onto the surface of silicalite-1 (S-1). With the optimal GaOx/MFI catalyst, the propane conversion and propylene selectivity reached 22.9 and 90.1%, respectively, in the propane dehydrogenation reaction. The work offers a clean and economical strategy utilizing liquid metal (LM) as an impregnation solution for the preparation of GaOx-based catalysts.

Boronate affinity metal–organic frameworks molecularly imprinted membranes with hierarchical porous channels for the selective separation of naringin

Naringin (NRG), known as an important natural flavoniod compounds, exhibits excellent phamaceutical value and clinical application prospect. However, the main obstacle to the isolation and purification of NRG is the low concentration and complexity of the extraction system. Herein, a new kind of hierarchical porous metal–organic frameworks (MOFs) based molecularly imprinted membranes (PBMMA-MIMs) for the specific separation of NRG. The prepared PBMMA-MIMs showed the fast adsorption kinetics (within 120 min). Moreover, the abundant boronic acid imprinted recognition sits and hydrophilic hierarchical porous MOFs improved the adsorption capacity (the maximum adsorption amounts 57.39 μmol/g) and exhibited selective NRG adsorption (imprinting factor 2.31) with efficiency over 91.69 % after seven adsorption–desorption cycles. In addition, the coarse NRG could be effectively extracted to a promising purity of 93.13 % via PBMMA-MIMs. This study provides new insights into the design molecularly imprinted membranes via environmentally friendly synthesis route for the preparation for enriching high-value flavoniods, achieving efficient purification rate of agricultural wastes for pollution control, and promoting the sustainable reuse in complex agricultural wastewater.

Unveiling the low‐temperature oxidation chemistry of dipropyl carbonate

AbstractDialkyl carbonates (DACs) own an environmentally friendly synthesis route, making them potential candidates as alternative fuels. However, for DACs to be widely accepted as an alternative fuel, a comprehensive understanding of their combustion behavior is essential. Dipropyl carbonate (DPrC) represents a transition from short‐chain to mid‐chain carbonates, understanding its combustion behaviors holds significance in unraveling the combustion chemistry of carbonates. In this study, the oxidation of DPrC was investigated with the initial fuel mole fraction of 0.5% at three equivalence ratios of 0.5, 1.0, and 2.0 within a temperature range of 550–1100 K in a jet‐stirred reactor for the first time. Gas chromatography was utilized for the quantitative detection of reactants, intermediates, and products. A detailed DPrC mechanism was first developed, and good agreements between measurements and simulations were obtained. A notable negative temperature coefficient (NTC) behavior was first observed in the oxidation of DACs. Such NTC phenomenon occurred at fuel‐lean conditions in the temperature range of 620–660 K, while only a weak low‐temperature consumption was observed at the stoichiometric condition. Kinetic modeling studies showed that this unique low‐temperature chemistry of DPrC can be attributed to the differences in the RO2 isomerization reactions between DPrC and short‐chain DACs. The RO2 isomerization via a six‐member ring transition state could happen in DPrC oxidation but not in dimethyl carbonate and diethyl carbonate oxidation, due to the different fuel molecular structure. Therefore, the subsequent reaction pathways via QOOH → O2QOOH → HO2Q = O + OH → OQ = O + OH were promoted and two OH radicals were released in this process. Moreover, it is conceivable that mid or long‐chain DACs could also exhibit an NTC phenomenon due to the increased potential for RO2 isomerization via a six‐ or seven‐member ring transition state, thereby increasing the likelihood of RO2 isomerization occurrence.

Retraction: Gallic Acid Grafted to Amine‐Functionalized Magnetic Nanoparticles as a Proficient Catalyst for Environmentally Friendly Synthesis of α‐Aminonitriles

Retraction: Gallic Acid Grafted to Amine‐Functionalized Magnetic Nanoparticles as a Proficient Catalyst for Environmentally Friendly Synthesis of α‐Aminonitriles

Preparation and investigation of structural, optical, and dielectric properties of PVA/PVP blend films boosted by MWCNTs/AuNPs for dielectric capacitor applications

With the rising global energy demands, there is a pressing need for the invention of efficient and reliable energy storage systems. This research centers on the creation and analysis of flexible dielectric capacitors composed of polymer nanocomposites (PNCs), incorporating a blend of polyvinyl alcohol (PVA) and polyvinyl pyrrolidone (PVP) as the base polymer, with multi-walled carbon nanotubes (MWCNTs) and gold nanoparticles (AuNPs) serving as nanofillers. The AuNPs were produced through an environmentally friendly synthesis method. Films made from PVA/PVP blended with MWCNTs and AuNPs were fabricated using the casting approach. Various characterization methods, including TEM, XRD, FTIR, and UV–Vis spectroscopy, were utilized to evaluate the samples. A detailed analysis of their electrical/dielectric characteristics was conducted. XRD analysis revealed a significant decrease in crystallinity from 55% for the pure PVA/PVP blend to 37% for the 1.6 wt% nanofiller composite, indicating increased amorphous content, which facilitates better ion mobility. FTIR confirmed strong interactions between the polymer matrix and nanofillers, with intensified vibrational peaks pointing to enhanced molecular dynamics. UV–Vis spectroscopy demonstrated a red shift in the absorption edge, and Tauc plot analysis showed a reduction in the indirect/direct optical band gap from 4.84 eV/5.68 eV for the pure blend to 4.26/5.35 eV for the nanocomposite with 1.6 wt% nanofillers. The addition of nanofillers resulted in improvements in their dielectric features, which exhibited a significant performance improvement, with the dielectric constant (ε′) reaching approximately 1100 at low frequency for the 1.6 wt% nanofiller sample, compared to 9 for the pure blend. Additionally, the dielectric loss (ε'') and tangent loss (tan δ) were reduced, with tan δ showing a decrease from 15 for the pure blend to 2 for the 1.6 wt% nanofiller composite at low frequency, indicating enhanced dielectric efficiency and reduced energy dissipation. The capacitors' functionality was assessed through capacitance-frequency and conductance-frequency analyses. The capacitors exhibited stable high capacitance across a broad frequency spectrum, making them alternatives for energy storage solutions.

Mechanochemical synthesis and characterization of poly[(aniline-co-N-(4-sulfophenyl) aniline] nanofibers and its nanocomposite with titanium dioxide nanoparticles and study of their efficiency in hybrid solar cell

The advantages of polyaniline for application in new generation solar cells include its cost-effectiveness, environmentally friendly synthesis, remarkable stability, and the ability to modify the bandgap through the synthesis of its nanocomposites. But a challenge for its nanostructures is the limited solubility in non-toxic solvents, including water, which limits their processability in coating techniques. We overcame this challenge by synthesizing its copolymer with diphenylamine-4-sulfonate and its nanocomposite with titanium dioxide nanoparticles (TiO2NPs). So through a solid-state and template-free technique and using sodium diphenylamine-4-sulfonate, aniline hydrochloride salt, TiO2NPs, and FeCl3∙6 H2O as an oxidant, poly(N-(sulfophenyl)aniline) nanoflowers (PSANFLs), poly [(aniline-co-N-(4-sulfophenyl) aniline] nanofibers (PAPSANFs), poly(N-(sulfophenyl)aniline) nanofibers/titanium dioxide nanoparticles (PSANFs/TiO2NPs), and poly (aniline-co-N-(4-sulfophenyl)aniline nanofibers/titanium dioxide nanoparticles (PAPSANFs/TiO2NPs) were synthesized. Characterization of the synthesized samples was carried out through field emission scanning electron microscopy (FE-SEM), Fourier-transform infrared spectra, ultraviolet-visible spectra (UV-Vis), cyclic voltammetry (CV), and elemental analysis (CHNS). The FE-SEM images clearly illustrate that the synthesized samples are of nanoscale dimensions. The band gap values of 2.23 eV for PSANFs/TiO2NPs and 1.96 eV for PAPSANFs/TiO2NPs nanocomposites were determined through electrochemical calculations based on cyclic voltammetry curves, showcasing the complementary properties of n and p semiconductors. Using doctor blade method to prepare films from synthesized materials and the architectural pattern of ITO│TiO2NPs│semiconductor sample│Al, all hybrid solar cells are fabricated. The I-V characteristics and power conversion efficiency (PCE) of the samples were examined and discussed. The PCE values for the four samples were found to be in the range of 0.20–0.82 %.

Green Synthesis of Dracocephalum kotschyi-Coated Silver Nanoparticles: Antimicrobial, Antioxidant, and Anticancer Potentials.

BACKGROUND The environmentally friendly production of silver nanoparticles (AgNPs) has gained significant attention as a sustainable alternative to traditional chemical methods. This study focused on synthesizing AgNPs using extract of Dracocephalum kotschyi (D. kotschyi), a medicinal plant. MATERIAL AND METHODS The biosynthesis of AgNPs was monitored using UV-visible spectrophotometry. The role of phytoconstituents from D. kotschyi in stabilizing AgNPs was analyzed using Fourier-transform infrared (FTIR) spectroscopy. Dynamic light scattering (DLS) spectroscopy was used to determine the size, charge, and polydispersity of the nanoparticles, while scanning electron microscopy (SEM) was employed to assess their morphology. We evaluated the antimicrobial efficacy of the synthesized AgNPs against various bacteria, their antioxidant properties via a 2,2-Diphenyl-1-picrylhydrazyl (DPPH) assay, and their cytotoxic activity against the HeLa cervical cancer cell line. RESULTS The formation of AgNPs was indicated by a color change and the emergence of a surface plasmon resonance peak at 418 nm. The nanoparticles demonstrated significant antimicrobial, antioxidant, cytotoxic, and anticancer activities. Morphology, size, and shape analysis revealed nearly spherical particles with an average size of 43 nm. FTIR confirmed the presence of phenolic compounds in the extract, serving as reducing and capping agents. X-ray diffraction (XRD) analysis confirmed the crystalline structure of the nanoparticles. Antimicrobial assessments showed effectiveness against Escherichia coli and Staphylococcus aureus. The DPPH scavenging assay demonstrated efficient antioxidant activity, and potent apoptotic anticancer effects were observed on cervical cancer cells. CONCLUSIONS The extract of D. kotschyi was effective as a reducing agent in the environmentally friendly synthesis of AgNPs, which exhibited noteworthy antimicrobial, antioxidant, and anticancer properties. These findings suggest potential biomedical applications for the synthesized AgNPs.

Green synthesis of Ag/AgCl nanocomposites derived from Muntingia calabura L. leaves extract: antioxidant properties and catalytic activity in methylene blue degradation

ABSTRACT Ag/AgCl nanocomposites were synthesised using Muntingia calabura L. leaves extract for the first time and were used as antioxidants and catalysts in the degradation of methylene blue (MB). This study aimed to achieve the optimal conditions for synthesising Ag/AgCl nanocomposites using Muntingia calabura L. leaves extract and to examine their antioxidant and photocatalytic activities. Ag/AgCl nanocomposites were confirmed using UV-Vis spectroscopy, Fourier transform-infrared (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), and Zeta Potential analysis. Optimising various factors revealed that the optimum synthesis of Ag/AgCl nanocomposites involved mixing 3 mL of 2.5 mm AgNO3 with 7.5 mL of the extract and stirring continuously at 60°C for 100 min. The formed Ag/AgCl nanocomposites displayed mainly spherical shapes with some irregular forms, maintaining an average size of 69.04 nm and remaining stable for 6 months. In vitro studies on antioxidant activity using DPPH indicated that the Ag/AgCl nanocomposites exhibited outstanding free radical scavenging activity, with an IC50 of 62.76 mg/L. In addition, Ag/AgCl nanocomposites showed a strong photodegradation potential for MB, with a degradation percentage of up to 82.12% in 210 min. Hence, the results offer a promising approach for the environmentally friendly synthesis of Ag/AgCl nanocomposites using Muntingia calabura L. leaves extract, with significant applications in antioxidants and photocatalysts.

Green Synthesis of Silver Nanoparticles Using <i>Citrus sinensis</i> Peels Assisted by Microwave Irradiation as a Contrast Agents for Computed Tomography Imaging

Contrast agents are extensively used to enhance the quality of images in computed tomography (CT) scans for brain exams, vascular imaging, and full-body imaging. Recent data indicate that iodine-based contrast agents have brief durations of blood circulation and may lead to harmful toxicity effects. This study aims to produce silver nanoparticles using environmentally friendly synthesis techniques facilitated by microwaves. The characteristics of nanoparticles have been studied using UV-vis, FTIR, XRD, and TEM techniques. The TEM analysis reveals that the silver nanoparticle has an average diameter of 9 nm and exhibits a spherical shape. The contrast-to-noise ratio (CNR) values of silver nanoparticles at 100, 150, and 200 mg/L concentrations are 35.79, 48.16, and 74.66, respectively. In comparison, iodine exhibits CNR values of 28.57, 34.69, and 48.56 at the same concentrations. The CNR values for tube currents of 140, 160, and 180 mA are 37.83, 44.98, and 48.26, respectively. In contrast, the CNR values in silver nanoparticles are 63.64, 75.32, and 81.67. The results obtained from the different concentrations and tube currents clearly demonstrate that silver nanoparticles have a higher CNR than iopamidol. Hence, silver nanoparticles have significant potential as contrast agents.

Environmentally Friendly Synthesis of Gelatin Hydrogel Nanoparticles for Gastric Cancer Treatment, Bisphenol A Sensing and Nursing Applications: Fabrication, Characterization and ANN Modeling

This study presents a dual application approach for the environmentally friendly synthesis of gelatin hydrogel nanoparticles with potential applications in gastric cancer treatment, bisphenol A (BPA) sensing, and nursing. Gelatin hydrogel nanoparticles were synthesized using a green and freeze-drying method, avoiding the use of toxic chemicals and solvents. The nanoparticles showed excellent biocompatibility and promising potential for drug delivery system (DDS) in gastric cancer treatment. The controlled release of anticancer drugs from the gelatin nanoparticles was showed, highlighting their potential in targeted therapy. Additionally, the gelatin hydrogel nanoparticles were explored for BPA sensing. BPA is a widely used chemical known for its adverse effects on human health. The gelatin nanoparticles showed high selectivity and sensitivity towards BPA detection, making them suitable for environmental monitoring and health applications using scanning electron microscope (SEM). Also, in this study, an artificial neural network (ANN) was used to estimate the release of docetaxel (%) at 72 hours, the release of paclitaxel (%) at 72 hours, tensile strength with sample (wt%), and porosity (%) in broader ranges than the experimental samples. The environmentally friendly synthesis of gelatin hydrogel nanoparticles presented in this study offers a versatile platform with dual applications in gastric cancer treatment and sensing of harmful chemicals. The obtained results show the potential of these nanoparticles for innovative therapeutic and diagnostic strategies in healthcare and environmental monitoring. The study showed the development of sustainable and multifunctional nanomaterials for various biomedical applications. The modeling of the neural network predictions shows that increasing the sample (wt%) and porosity (%) leads to an increase in the release of docetaxel (%) at 72 hours, the release of paclitaxel (%) at 72 hours, and tensile strength. As porosity decreases, the release of docetaxel increases, and the release of paclitaxel and tensile strength also increase. Additionally, the prediction errors of the ANN in this study were evaluated using linear regression, showing acceptable error rates compared to the target results obtained from the experimental tests.

Direct synthesis of low-silica ZSM-48 zeolite via seed-assisted hydrothermal synthesis with 1,6-hexanediamine as template

ZSM-48 zeolite is characteristic of 10-member ring (10-MR) one-dimensional tubular channel structure and finds extensive applications in catalytic hydroisomerization reactions. Here we developed an efficient synthetic strategy for low-silica ZSM-48 zeolite with a SiO2/Al2O3 ratio at 30∼176 via a seed-assisted hydrothermal synthesis method, overcoming the limit that 1,6-hexanediamine (HDA) template can only be used to synthesize high-silica (i.e., SiO2/Al2O3 ratio >200) zeolites. A two-step crystallization procedure coupled with zeolite seed-assisted synthesis strategy was enrolled to realize well crystallized ZSM-48 zeolites, in which the zeolite nuclei are sufficiently produced at the nucleation temperature at 100 °C for 24 h with the aid of zeolite seeds, and the zeolite growth is proceeded at the crystallization temperature at 160 °C for 48 h. The morphology and particle size of low-silica ZSM-48 have been manipulated by adjusting the synthetic parameters, such as the alkalinity and silicon source of aluminosilicate gel for zeolite, the crystallization manner (static or dynamic crystallization), as well as the presence of additive (i.e., sodium chloride). The as-synthesized ZSM-48 zeolite exhibits a significantly high acid content of 0.194 mmol/g, highlighting its potential as an excellent acidic support for hydroisomerization catalysts. The cost-effective and environmentally friendly synthesis strategy, which is anticipated to expand the application of alkylamine organic templates in the synthesis of low-silica ZSM-48 zeolite.

Xanthenes: Novelty and Green Photocatalysis for the Formation of Carbon-carbon or Carbon-heteroatom Bond

: This review covers photoreduction reactions using xanthenes reported from 2011 to date and compares them with the conventional photocatalytic method. Xanthenes have strong absorption in the visible light spectrum (520-550 nm), and their redox potential resembles organometallic complexes, such as those containing Ir or Ru, and they are also easy to handle and accessible. In addition to being metal-free, photocatalysis with xanthenes is performed under mild reaction conditions. For instance, no radical initiators are needed because the energy sources are led devices or household lamps, most reactions are performed at room temperature in common solvents (MeOH, MeCN, acetone, DMSO), and an anhydrous or inert atmosphere is usually not required. As a result, xanthene dyes hold the promise of a more environmentally friendly synthesis of organic compounds.

Structural and luminescence properties of Y2O3:Ho3+ phosphor: Potential applications in plant cultivation LEDs and thermoluminescent dosimetry

Current research on Y2O3:Ho3+ phosphors highlight their promising luminescence properties, but often lacks an environmentally friendly synthesis method and comprehensive analysis of their applications. In this study, we address these gaps by successfully synthesizing Y2O3:Ho3+ phosphors using a green synthesis route with varying concentrations of Ho3+. Our work provides detailed characterization of their photoluminescence (PL) and thermoluminescent (TL) properties. The PL excitation (PLE) spectra reveal a distinct peak at 439 nm, attributed to the 5I8→(5K5; 5G5) transition of Ho3+ions. Upon excitation at 439 nm, the emission spectra show a sharp emission peak around 660 nm from the 5F5→5I8 transition, with the 0.1 mol% Ho3+ phosphors exhibiting particularly strong red emission, indicating their suitability for indoor plant cultivation under LED lighting. Additionally, TL properties were evaluated after gamma-ray exposure, with the highest emission intensity at 0.1 mol% Ho3+ concentration. TL glow curves were analyzed for various radiation doses using the Computerized Glow Curve Deconvolution (CGCD) method, and TL trapping parameters were determined through Chen's peak shape and the Initial Rise methods. This work demonstrates significant potential for using these phosphors to enhance indoor plant growth and for applications in thermoluminescent dosimetry (TLD).

Green-synthesized silver nanoparticles from Zataria multiflora as a promising strategy to target quorum sensing and biofilms in Pseudomonasaeruginosa

The global challenge to human health is significantly heightened by the resistance of harmful bacteria to antimicrobial treatments. Given the limited advancement in developing new antimicrobial medications, exploring innovative strategies is imperative to tackle the challenge of resistance to multiple drugs. Furthermore, there is a growing emphasis on the environmentally friendly synthesis of nanoparticles with potent medicinal attributes, specifically those targeting virulence, to combat the rise of multidrug resistance. Focusing on the inhibition of virulence factors and biofilms influenced by quorum sensing has become a promising and novel strategy in the development of anti-infective drugs. An aqueous extract of Zataria multiflora leaves was used to create green-synthesized silver nanoparticles, or AgNPs. X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and UV–visible absorption spectroscopy were used to characterize the AgNPs. The impact of AgNPs on the virulence factors and biofilms of Pseudomonas aeruginosa PAO1, mediated by quorum sensing, was assessed at concentrations below the minimum inhibitory concentration (sub-MIC). Sub-MIC concentrations of Green-synthesized AgNPs inhibited various P. aeruginosa virulence factors, including bacterial motility (89 % inhibition), pyocyanin production (81.48 % inhibition), pyoverdin production (55.80 % inhibition), elastase activity (87.43 % inhibition), exoprotease activity (75.60 % inhibition), and rhamnolipid production (71.28 % inhibition). Additionally, these AgNPs demonstrated 80 % inhibition of P. aeruginosa biofilms. The in vitro efficacy of green-synthesized AgNPs against P. aeruginosa can be utilized for the creation of alternative therapeutic agents for managing bacterial infections, particularly for topical application in cases such as wound infections. Additionally, they can be used for surface coating to inhibit the attachment of bacteria to medical devices.

Comparative Studies of Benzimidazoles Synthetic Routes and its Biological Activity

<p> Benzimidazole, discovered in 1872, is a heterocyclic compound noted for its pharmacological activities. It and its derivatives can be synthesized through methods such as condensation reactions and using nano-based nanoparticles as catalysts. Recent environmentally friendly methods include microwaves, ultrasound, and photochemical reactions. its derivatives are known for their diverse medicinal applications </p> <p> Benzimidazole and its derivatives are versatile compounds with a wide range of pharmacological activities. Their synthesis has evolved over time, incorporating various environmentally friendly methods such as microwave, ultrasound, and photochemical reactions. The continued exploration of these compounds and their synthesis methods holds great promise for the development of new and effective medicinal applications. </p> <p> Here, we provide an overview of benzimidazole, highlighting its historical significance, various synthesis methods, and extensive range of pharmacological activities. It aims to emphasize the importance of benzimidazole and its derivatives in medicinal chemistry and their potential therapeutic applications. The review also notes the development of environmentally friendly synthesis techniques, reflecting advancements in the field.</p>

Achieving Record C2H2 Packing Density for Highly Efficient C2H2/C2H4 Separation with a Metal–Organic Framework Prepared by a Scalable Synthesis in Water

AbstractAdsorptive C2H2/C2H4 separation using metal–organic frameworks (MOFs) has emerged as a promising technology for the removal of C2H2 (acetylene) impurity (1 %) from C2H4 (ethylene). The practical application of these materials involves the optimization of separation performance as well as development of scalable and green production protocols. Herein, we report the efficient C2H2/C2H4 separation in a MOF, Cu(OH)INA (INA: isonicotinate) which achieves a record C2H2 packing density of 351 mg cm−3 at 0.01 bar through high affinity towards C2H2. DFT (density functional theory) calculations reveal the synergistic binding mechanism through pore confinement and the oxygen sites in pore wall. The weakly basic nature of binding sites leads to a relatively low heat of adsorption (Qst) of approximately 36 kJ/mol, which is beneficial for material regeneration and thermal management. Furthermore, a scalable and environmentally friendly synthesis protocol with a high space‐time yield of 544 kg m−3 day−1 has been developed without using any modulating agents. This material also demonstrates enduring separation performance for multiple cycles, maintaining its efficacy after exposure to water or air for three months.

Sustainable Removal of Cr(VI) from Wastewater Using Green Composites of Zero-Valent Iron and Natural Clays

Composites for efficient removal of hexavalent chromium Cr(VI) from industrial wastewater were obtained by deposition of nano-zero-valent iron (nZVI), synthesized by environmentally friendly synthesis using oak leaf extract, on inexpensive, natural, readily available and cheap natural raw materials, sepiolite (SEP) or kaolinite/illite (KUb) clay, as support. nZVI particles were deposited from the FeCl3 solution of different concentrations, with the same volume ratio extract/FeCl3 solution (3:1), and with different masses of SEP or KUb. Physico–chemical characterization (SEM/EDS, FTIR, BET, determination of point of zero charge) of the composites and nZVI was performed. The results of SEM and BET analyses suggested more homogeneous deposition of nZVI onto SEP than onto KUb, which ensures greater availability of the nZVI surface for Cr(VI) anions. Therefore, the higher Cr(VI) removal at all investigated initial pH values (pHi) of the solution (3, 4 and 5) was achieved with the SEP composites. The adsorption results indicated that the elimination of Cr(VI) was achieved via the combined effect of reduction and adsorption. The removal of total chromium at pHi = 3 was approximately the same as that of Cr(VI) removal for the KUb composites, but lower for the SEP composites, indicating lower removal of Cr(III) compared to the reduced Cr(VI). The SEP/nZVI composite with the highest removal efficiency was applied for Cr(VI) removal from real wastewater at pHi = 3 and pHi = 5. The results demonstrated the high Cr(VI) removal capacity, validated the assumption that a good dispersion of nZVI particles is beneficial for Cr(VI) removal and showed that the produced green composites can be efficient materials for the removal of Cr(VI) from wastewater.

Achieving Record C2H2 Packing Density for Highly Efficient C2H2/C2H4 Separation with a Metal-Organic Framework Prepared by a Scalable Synthesis in Water.

Adsorptive C2H2/C2H4 separation using metal-organic frameworks (MOFs) has emerged as a promising technology for the removal of C2H2 (acetylene) impurity (1%) from C2H4 (ethylene). The practical application of these materials involves the optimization of separation performance as well as development of scalable and green production protocols.Herein, we report the efficient C2H2/C2H4 separation in a MOF, Cu(OH)INA (INA: isonicotinate) which achieves a record C2H2 packing density of 351 mg cm-3 at 0.01 bar through high affinity towards C2H2. DFT (density functional theory) calculations reveal the synergistic binding mechanism through pore confinement and the oxygen sites in pore wall.The weakly basic nature of binding sites leads to a relatively low heat of adsorption (Qst) of approximately 36 kJ/mol, which is beneficial for material regeneration and thermal management. Furthermore, a scalable and environmentally friendly synthesis protocol with a high space-time yield of 544 kg m-3 day-1 has been developed without using any modulating agents. This material also demonstrates enduring separation performance for multiple cycles, maintaining its efficacy after exposure to water or air for three months.

Electrochemical Synthesis of Metal‐Organic Frameworks Based on Zinc(II) and Mixed Ligands Benzene‐1,4‐Dicarboxylate (BDC) and 4,4′‐Bipyridine (Bpy) and its Preliminary Study on CO2 Adsorption Capacities

AbstractEfficient and environmentally friendly synthesis methods for metal‐organic frameworks (MOFs) have emerged as a compelling topic in the organometallic field. In this study, we successfully electro‐synthesized a MOF based on mixed ligands, benzene‐1,4‐dicarboxylate (BDC) and 4,4′‐bipyridine (Bpy), denoted as MOF‐508b, and investigated its CO2 adsorption capacity, comparing it with that of Zn‐BDC and Zn‐Bpy coordination polymers. Unlike the circular shapes of Zn‐BDC and Zn‐Bpy, MOF‐508 adopts a three‐dimensional structure upon binding with the pillar ligand, featuring mesoporous pore sizes. MOF‐508b demonstrates superior stability at room temperature, exhibiting a thermal stability of 400 °C. The CO2 capture potential of the materials was assessed under low‐pressure conditions at room temperature. The pillared layer of MOF‐508b results in the reduction of open metal sites, facilitating the binding of active CO2 through coordination, thereby influencing its optimum CO2 adsorption capacity (2.51 mmol g−1), which was found to be lower than that of Zn‐Bpy (3.83 mmol g−1) and Zn‐BDC (4.46 mmol g−1). The adsorption mechanism on MOF‐508b follows the Weber‐Morris model, emphasizing diffusion within particles over direct attachment to the material surface.