Reduction Of 4-nitrophenol Research Articles

Eco-friendly fabrication of MNP@MPN film capillary microreactors for enhanced catalysis and sensitive nitrite detection

A pioneering, eco-friendly methodology has been developed for the immobilization of metal nanoparticles embedded in metal phenolic networks (MNPs@MPNs) on the inner surfaces of capillary microreactors, eliminating the need for redox reagents. This innovative approach enables precise control over the MPN film thickness and the loading capacity of MNPs. The microreactor functionalized with this novel film exhibited exceptional catalytic performance in the reduction of 4-nitrophenol by sodium borohydride, achieving a near-quantitative conversion efficiency of 100%. Furthermore, we highly sensitively detected nitrite by assembling MNP@MPN microreactors as cascade reactors. The successful scale-up of this methodology to larger microreactors not only validates its versatility but also underscores its immense potential for implementation in the chemical industry, paving the way for more sustainable and efficient chemical processes.

Microwave assisted green synthesis of palladium nanoparticles using dragon fruit peel extract for catalytic reduction of 4-nitrophenol and methylene blue

Microwave assisted green synthesis of palladium nanoparticles using dragon fruit peel extract for catalytic reduction of 4-nitrophenol and methylene blue

Crystallinity regulation of ZIF-67 via defective MgO layer made by high voltage-assisted oxidation approach for optimal 4-nitrophenol reduction

Due to their unique structural characteristics, metal-organic frameworks (MOFs) have emerged as favorable contenders for photocatalytic applications. In this study, the crystallization of ZIF-67, a subclass of MOFs, on Mg and MgO substrates via dip coating was explored, and the resulting materials were employed as a photocatalyst for the 4-nitrophenol reduction. Due to the defective surface resulting from plasma activity during the high-voltage-assisted oxidation of AZ31 Mg alloy, MgO significantly impacts the crystallization of ZIF-67. This influence promotes the formation of a stable foundation and strong bonds, contributing to the emergence of a regular and symmetrical structure. This differs from the asymmetrical and irregular structure observed in ZIF-67@Mg when ZIF-67 is grown directly on the Mg substrate. Hence, the ZIF-67@MgO catalyst demonstrated remarkable enhancements in the reduction of 4-nitrophenol to 4-aminophenol, achieving an efficiency of approximately 97.12 % within 12 min under visible light. Importantly, the catalyst exhibited no stability decay even after ten consecutive cycles, surpassing the performance of previously reported catalysts. This research sheds light on the superior capabilities of ZIF-67@MgO in the context of visible-light-driven reduction of 4-NP. The results suggest potential for future progress in creating effective and eco-friendly photocatalytic materials for addressing environmental challenges.

Effect of Gold Nanoparticle Size on Regulated Catalytic Activity of Temperature-Responsive Polymer-Gold Nanoparticle Hybrid Microgels.

Gold nanoparticles (AuNPs) possess attractive electronic, optical, and catalytic properties, enabling many potential applications. Poly(N-isopropyl acrylamide) (PNIPAAm) is a temperature-responsive polymer that changes its hydrophilicity upon a slight temperature change, and combining PNIPAAm with AuNPs allows us to modulate the properties of AuNPs by temperature. In a previous study, we proposed a simpler method for designing PNIPAAm-AuNP hybrid microgels, which used an AuNP monomer with polymerizable groups. The size of AuNPs is the most important factor influencing their catalytic performance, and numerous studies have emphasized the importance of controlling the size of AuNPs by adjusting their stabilizer concentration. This paper focuses on the effect of AuNP size on the catalytic activity of PNIPAAm-AuNP hybrid microgels prepared via the copolymerization of N-isopropyl acrylamide and AuNP monomers with different AuNP sizes. To quantitatively evaluate the catalytic activity of the hybrid microgels, we monitored the reduction of 4-nitrophenol to 4-aminophenol using the hybrid microgels with various AuNP sizes. While the hybrid microgels with an AuNP size of 13.0 nm exhibited the highest reaction rate and the apparent reaction rate constant (kapp) of 24.2 × 10-3 s-1, those of 35.9 nm exhibited a small kapp of 1.3 × 10-3 s-1. Thus, the catalytic activity of the PNIPAAm-AuNP hybrid microgel was strongly influenced by the AuNP size. The hybrid microgels with various AuNP sizes enabled the reversibly temperature-responsive on-off regulation of the reduction reaction.

Catalytic degrading agents for dyes from pyrimidine derived imine capped nickel nanoparticles: Colorization of cotton and antibacterial activity of colored cotton

In this multifaceted experimental study, Schiff base (SL) stabilized nickel nanoparticles (SL-NiNPs) were synthesized and comprehensively characterized for their diverse applications. The synthesis process involved the formation of these nanoparticles through the reduction of ethanolic nickel chloride with sodium borohydride (NaBH4) under nitrogen gas, followed by their stabilization in toluene using tetraoctylammonium bromide (TOAB) as phase transfer agent and SL as capping agent. Characterization studies confirmed the successful synthesis and stabilization of SL-NiNPs, with UV-Vis spectral analysis, SEM, and TEM revealing their distinctive properties, including a spherical shape and a size of approximately 50 nm. The catalytic properties of SL-NiNPs was demonstrated in several reactions, including the reduction of 4-nitrophenol to 4-aminophenol, the degradation of methylene blue, and the reduction of methyl orange. These catalytic reactions showcased the efficiency and versatility of SL-NiNPs as effective catalysts for environmental and chemical processes. Furthermore, SL-NiNPs were employed in the coloration of cotton, leading to surface modification with nano-sized particles. SEM imaging illustrated the successful modification of cotton, enhancing its surface properties. The antimicrobial potential of SL-NiNPs-embedded cotton was assessed against various bacterial strains, revealing a dose-dependent inhibitory effect. As the concentration of SL-NiNPs increased, the diameter of the inhibition zones also increased, further emphasizing the potent antibacterial properties of these materials.

Facile synthesis of nickel doped ZnO and CeO2 nanocomposite for efficient photocatalytic dye degradation, catalytic reduction and antimicrobial studies

The current research work reports on binary Nickel oxide-Zinc oxide (NiO-ZnO) and Nickel oxide-Cerium oxide (NiO-CeO2) nanocomposites synthesis by facile single step in-situ thermal decomposition method and its applications. The structural and morphological studies were examined using various characterization techniques like IR, UV-DRS, XRD and SEM with EDAX studies. The IR bands at 545-533 cm−1 corresponds to M-O stretching vibration. The XRD studies confirms the structural pattern of NiO-ZnO and NiO-CeO2 nanocomposites. SEM with EDAX results reveal the structure, composition and purity of synthesized nanocomposites. The nanocomposites were employed as photocatalyst for degradation of methylene blue and methyl orange dyes and as a catalyst toward 4-nitrophenol reduction. Antibacterial studies against E. coli (Gram-negative) and S. aureus (Gram-positive) bacterial pathogens were carried out using the nanocomposites. The outcomes show 97% efficiency in forty minutes for catalysis and 120 min for dye degradation and a better zone of inhibition in antibacterial studies for NiO-ZnO nanocomposite. The comparative result for both the nanocomposites discloses that the photocatalytic degradation, catalytic and antimicrobial efficiency of NiO-ZnO nanocomposite is more efficient than NiO-CeO2 nanocomposite. The results reveal the outstanding catalytic and dye degradation and antibacterial activity of NiO-ZnO than NiO-CeO2.

Modification of new magnetic nanocomposites Bi2WO6/CuFe2O4 and its excellent catalytic reduction for toxic nitroaromatic compounds and chromium (VI)

New magnetic Bi2WO6/CuFe2O4 nanocomposites were synthesized using hydrothermal method. The specific features of Bi2WO6/CuFe2O4 nanocomposites were studied using various analytical techniques such as Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM) and N2 adsorption desorption analyses, Brunauer-Emmett-Teller (BET). The BET analysis demonstrates that embedded CuFe2O4 nanoparticles in Bi2WO6 structure have increased the pore diameters and surface area for better adsorption of NaBH4 and catalytic performance. The VSM analysis confirms the magnetic behavior of nanocomposite which showed that Bi2WO6/CuFe2O4 could be separated and recoverd easily by an external magnet after catalytic reactions. The catalytic performance of nanocomposites was investigated for the reduction of nitroaromatic compounds including 4-nitroaniline (4-NA), 4-nitrophenol (4-NP), 2-nitroaniline (2-NA) and 2-nitrophenol (2-NP) and chromium (VI) in aqueous solution. The results show the nanocomposites have excellent ability to reduces Cr(VI) to Cr(III) and nitroaromatic compounds to the corresponding amines in green water solution at room temperature. The best performance observed for the 100% conversion of 4-nitrophenol reduction belongs to Bi2WO6/CuFe2O4 20%, which completes in 6 min, and its rate constant is about 0.67 min−1. In addition, the Bi2WO6/CuFe2O4 nanocomposite can be appropriately recycled and reused several times without changing its structure and activity, which is essential for practical applications.

Spectroscopic monitoring of polyurethane-based nanocomposite as a potential catalyst for the reduction of dyes

In this study, AgNPs-loaded polyurethane-sodium alginate (PU-S/Alg) composite polymers were prepared by precipitation polymerization and in-situ reduction method. Their catalytic potential was evaluated for the reduction of methyl orange (MO), brilliant blue (BB), Rhodamine B (RhB), 4-nitroaniline (4-NA), and 4-nitrophenol (4-NP). Successful preparation of samples was confirmed by UV–Visible spectrophotometry (UV–Visible), Fourier transform infrared (FTIR), and Scanning electron microscopy (SEM) analysis. During the catalytic study, the value of kapp for the reduction of MO in the presence of NaBH4 and catalyst was found 0.488 min−1 while, in the presence of NaBH4 and catalyst alone, were found as 0.9 × 10-4 and 0.8 × 10-5 min−1, respectively which indicates the role of catalyst in making the reaction speedy. The value of kapp for the reduction of BB, RhB, 4-NA, and 4-NP was found as 0.764, 0.475, 0.212 and 0.757 min−1, respectively. Simultaneous reduction of dyes induced a decreased reaction completion time under the same reaction conditions. A slight increase in the value of kapp for the catalytic reduction of MO was also observed when reactions were performed in the presence of ionic media of different salts such as NaCl, KCl, CaCl2, and MnCl2. The rate of reduction of MO was increased with the increase in ionic strength of the medium. However, the presence of SDS (surfactant) in the reaction mixture induced the decreased activity of the catalyst and increased reaction completion time. The same value of kapp for the reduction of MO was observed in the case of freshly prepared and several days old nanocomposite catalyst. These results illustrate the stability and maintained catalytic potential of metal NPs for a prolonged time. Our reported catalyst also showed good potential for the treatment of dyes-polluted textile industry wastewater.

Catalytic Reduction of 4-Nitrophenol and Methylene Blue with Silver Nanoparticles Decorated with Drymoglossum piloselloides Extract

Drymoglossum piloselloides is one of the epiphytic plants that is commonly found in Southeast Asia region. In this study, the ethanol extract of D. piloselloides plant has been used in the green synthesis of silver nanoparticles. The synthesized silver nanoparticles were characterized by ultraviolet-visible (UV-Vis) spectrophotometry, X-ray diffraction (XRD),Fourier-transform infrared (FTIR) spectroscopy, and transmission electron microscopy (TEM) measurements. The UV-Vis spectrum of silver nanoparticles showed a maximum wavelength at 453 nm. The XRD measurement showed the silver nanoparticles peaks at 38.38°, 44.60°, 64.76°, and 77.62°. The FTIR spectra provided evidence of the interaction between silver and chemicals in the plant extract as a weak signal at 682 cm-1. Meanwhile, TEM revealed an average size of 12.63nm. The synthesised silver nanoparticles were utilised for the reduction of 4-nitrophenol with a conversion percentage of up to 100% with a reduction reaction rate constant of 7.104 s-1. In addition, methylene blue was also successfully reduced with the synthesised silver nanoparticles as the catalyst with a reduction reaction rate constant (k) of 21.150 s-1. This study highlights the superior advantage of utilizing ethanolic extract of D. piloselloides to prepare silver nanoparticles with promising catalytic reduction purposes.

Ag‐Based Bimetallic Nanoparticles for the Catalytic Reduction of Nitrophenol and Organic Dyes: An Overview

AbstractBimetallic nanoparticles with synergistic effects revealed much higher catalytic activity than respective monometallic materials. This review describes bimetallic nanoparticles, especially silver nanoparticles, combined with the other transition elements, such as Ag−Fe, Ag−Co, Ag−Ni, and Ag−Cu, as an enhanced catalytically active material. The coverage is given to the various methods of preparation, in which factors responsible for different structures of bimetallic nanoparticles are thoroughly discussed. Lastly, we explore the use of bimetallic nanoparticles as a catalyst for the degradation of numerous organic pollutants that contribute to water pollution.

Highly stable and efficient gold nanoparticles films facilitated by thiourea for catalytic reduction of nitrophenol in water

Water pollution from nitrophenol, a common nitrogen-containing aromatic pollutant, is becoming increasingly significant. Making the conversion of nitrophenol to the less toxic and more easily biodegradable aminophenol is a promising strategy to treat industrial wastewater. A simple and efficient method for treating nitrophenol was investigated using gold nanoparticles (AuNPs) with thiourea and fabricating AuNPs films via filtration for the first time. The prepared AuNPs film with nanoporous structure exhibits good structural stability and excellent catalytic activity. The results show that the optimal concentration of adding thiourea is 20 μg/mL, and the optimal concentration of adding NaBH4 is 1000 mM. After treatment with 20.0 μg/mL thiourea, the prepared AuNPs film catalyzes the degradation of 1.0 mM 2-nitrophenol to 2-aminophenol in just 150 sec. The AuNPs film provides a high density of active sites at the interface, and its stable nanoporous structure brings the substrate nitrophenol closer to the active center, thus enhancing the efficiency of catalytic reduction. Besides, the AuNPs films treated with thiourea still maintained good catalytic performance after seven cycles of catalysis and the catalytic efficiency is still as high as 90%. The thiourea-treated AuNPs film sets a precedent for the innovation of novel catalysts that is a very promising industrial strategy for reducing nitrophenol to aminophenol, offering significant economic advantages.

Highly Biocompatible Hemoglobin-Stabilized Gold Nanoparticles for an Enhanced Catalytic Reduction of 4-Nitrophenol

4-nitrophenol (4-NP) is a frequently encountered toxic phenolic organic pollutant in water. It is important to develop a simple method to treat 4-NP. Small and monodispersed gold nanoparticles often have good catalytic performance of 4-NP. Hemoglobin (Hb) is a kind of common and important protein in organisms. Herein, highly biocompatible bovine hemoglobin-stabilized gold nanoparticles (Aun-Hb NPs) were synthesized using hemoglobin as a biological template. Then, the size, zeta potential, and composition of Aun-Hb NPs were investigated by transmission electron microscopy, dynamic light scattering, and X-ray photoelectron spectroscopy. The Aun-Hb NPs with small gold nanoparticles of about 1.4–2.4 nm had good catalytic capabilities in reducing 4-NP to form 4-aminophenol. Au20-Hb NPs demonstrated superior catalytic efficiency in the reduction of 4-NP when compared to other nanoparticles. Moreover, as-synthesized Au20-Hb NPs exhibited excellent biocompatibility through the MTT experiment. The method of preparation of gold nanoparticles offers one way to prepare metal nanoparticles for good potential catalytic applications of gold nanoparticles.

Catalyst Supraparticles: Tuning the Structure of Spray-Dried Pt/SiO2 Supraparticles via Salt-Based Colloidal Manipulation to Control their Catalytic Performance.

The structure of supraparticles (SPs) is a key parameter for achieving advanced functionalities arising from the combination of different nanoparticle (NP) types in one hierarchical entity. However, whenever a droplet-assisted forced assembly approach is used, e.g., spray-drying, the achievable structure is limited by the inherent drying phenomena of the method. In particular, mixed NP dispersions of differently sized colloids are heavily affected by segregation during the assembly. Herein, the influence of the colloidal arrangement of Pt and SiO2 NPs within a single supraparticulate entity is investigated. A salt-based electrostatic manipulation approach of the utilized NPs is proposed to customize the structure of spray-dried Pt/SiO2 SPs. By this, size-dependent separation phenomena of NPs during solvent evaporation, that limit the catalytic performance in the reduction of 4-nitrophenol, are overcome by achieving even Pt NP distribution. Additionally, the textural properties (pore size and distribution) of the SiO2 pore framework are altered to improve the mass transfer within the material leading to increased catalytic activity. The suggested strategy demonstrates a powerful, material-independent, and universally applicable approach to deliberately customize the structure and functionality of multi-component SP systems. This opens up new ways of colloidal material combinations and structural designs in droplet-assisted forced assembly approaches like spray-drying.

Metal-organic frameworks (MOFs) wrapped palladium nanoparticles-loaded Fe3O4@CFR core-shell magnetic nanohybrid as heterogeneous catalyst with robust catalytic properties

Metal-organic frameworks (MOFs) wrapped palladium nanoparticles supported on Fe3O4@catechol formaldehyde resin (Fe3O4@CFR@Pd@MOF) as magnetic nanohybrid catalyst was successfully fabricated by employing the redox capacity of CFR shell of Fe3O4@CFR core-shell microsphere for in situ formation of Pd NPs, followed by surface coating with Cu-MOF(HKUST-1). The research results demonstrated that the complementary properties of the various components within this hybrid material yielded magnetic recyclable nanocatalysts with exceptional catalytic performance. The Fe3O4@CFR@Pd@MOF catalyst exhibited remarkable advantages in the catalytic reduction of nitrophenol, demonstrating a transformation frequency (TOF) value of up to 4651 h−1. Additionally, the nanocatalyst was proved to have robust catalytic capacity in the reduction of organic dyes and Suzuki-Miyaura reaction. The HKUST-1 framework played a triple role: facilitating dye enrichment, Cu2+ assisting Pd NPs catalysis, and mitigating Pd NPs leaching. Moreover, the synthesized catalyst exhibited favorable magnetic properties, enabling facile separation by magnets for efficient recycling and reutilization.

Enhancing catalytic activity through self-assembled hydrogen-bonded organic framework-based catalysts at liquid/liquid interface for 4-nitrophenol reduction and energy challenges in methanol fuel cell

Hydrogen-bonded organic frameworks (HOFs) are pure organic framework structures endowed with appropriate flexibility and porosity, which have attracted special attention in the field of energy and water, air, and soil remediation. In this study, six HOF-based materials were synthesized as thin film at the liquid/liquid (toluene/water) interface and characterized by FT-IR, Raman, UV–Vis, PXRD, ICP, AFM, SEM, TGA, and BET techniques. The self-assembled HOF-based thin films were employed as catalysts for the 4-nitrophenol removal from water medium and, for the first time, for methanol oxidation of fuel cell, with satisfying results. Simultaneous in situ catalyst formation and 4-nitrophenol reduction occurred in the case of Pt(0)@HOF thin film, but an extraordinary removal (not reduction) occurred in the presence of Pt(0)-trimesic acid thin film by formation of a new HOF from trimesic acid and 4-nitrophenol. Successful reduction of 4-nitrophenol occurred also in the presence of freshly prepared Pt(0)-trimesic acid, Pt(0)-melamine and Pt(0)@HOF catalysts (ex situ strategy). The chemical and thermal stability of HOF structure was improved by the interpenetration of ZIF-8 crystal structure, by increasing the hydrogen bonding and π-π stacking in the presence of 2-methylimidazole. The interpenetration of ZIF-8 to the crystal structure of HOF caused a significant decrease of the pore diameter of the structure. These pores acted as specific sites for the guest molecules, and their dimensions did not permit 4-nitrophenol to penetrate into the cavity of structures whereas allowed methanol penetration into these cavities due to its smaller size.

In situ green immobilization of palladium nanoparticles onto polydopamine-modified eggshell membrane for catalytic reduction of nitrophenols

4-Nitrophenol (4-NP) poses significant threats to both ecosystems and human health, making it essential and highly beneficial to take effective measures to mitigate its impact. Herein, eggshell membrane (ESM) with mussel-inspired polydopamine coatings (ESM-PDA) was constructed and utilized as a template for the immobilization of Pd NPs, resulting in ESM-PDA-Pd formation. The catalyst ESM-PDA-Pd exhibits exceptional performance in reducing 4-NP, and the TOF (turnover frequency) for ESM-PDA-Pd was determined to be 3.3 × 10−5 mmol·mg−1·min−1. Moreover, ESM-PDA-Pd demonstrates excellent catalytic activity in reducing other nitrophenols, including 2-nitrophenol (0.2196 min−1) and 2,4,6-nitrophenol (0.1177 min−1). Notably, the catalyst demonstrated brilliant recyclability, removing 92.4 % of 4-NP within 20 min after undergoing five consecutive runs. This underscores its potential for sustained and effective use in multiple cycles of nitrophenol reduction reactions. Furthermore, the measured Kapp in various water samples is as follows: ultrapure water (0.135 min−1) > tap water (0.109 min−1) > river water (0.083 min−1), indicating its significant potential for industrial applications.

Insight to the Catalytic Activity of Atomically Precise Ag4Ni2 Nanoclusters on Silicon Carbide for Nitroarene Reduction.

Atomically precise Ag4Ni2 nanoclusters with 2,4-dimethylbenzenethiol as the ligands were synthesized and characterized as a cocatalyst of SiC for the selective hydrogenation of nitroarenes to arylamine in the presence of NaBH4. The obtained Ag4Ni2/SiC samples exhibited extraordinary catalytic activity, and a self-accelerated catalytic process was observed with the reduction of nitrophenol to aminophenol as the model reaction. Experimental comparison between the Ag4Ni2/SiC samples before and after the catalysis showed that the transformation of Ag4Ni2 clusters to polydisperse Ag particles as well as amorphous NiOx on the surface of SiC in the catalysis was the key to their high activity. AIMD calculations revealed that the transformation of Ag4Ni2 was driven by the presence of multiple hydrides on the cluster, which induced the detachment of the thiol ligand of the nanoclusters.

A Catalytic Reduction of 4-Nitrophenol Utilizing Bimetallic CuO-Co3O4 Nanoparticles Synthesized via Wrightia tinctoria Extract: A Green Approach

In this investigation, copper oxide (CuO), cobalt oxide (Co3O4) and bimetallic copper oxide-cobalt oxide (CuO-Co3O4) nanoparticles were synthesized using an aqueous extract of Wrightia tinctoria leaves and characterized through UV-Vis, FT-IR, XRD, TEM and zeta potential analyses. The FT-IR analysis identified that specific phytoconstituents are responsible for the reduction and capping agents in nanoparticle synthesis. TEM analysis determined size and shape and zeta potential analysis assessed stability. The CuO and Co3O4 NPs, synthesized through an eco-friendly approach, were employed for 4-nitrophenol reduction with sodium borohydride. The reaction rate, was computed at 1 × 10-4 s-1, which indicated the pseudo-first-order kinetics. The synthesis of 4-aminophenol was also successfully acheived demonstrated that the excellent catalytic activity of CuO, Co3O4 and CuO-Co3O4 nanoparticles as catalysts.

Carbonized cellulose microspheres loaded with Pd NPs as catalyst in p-nitrophenol reduction and Suzuki-Miyaura coupling reaction

Catalytic reduction of p-nitrophenol is usually carried out using transition metal nanoparticles such as gold, palladium, silver, and copper, especially palladium nanoparticles (Pd NPs), which are characterized by fast reaction rate, high turnover frequency, good selectivity, and high yield. However, the aggregation and precipitation of the metals lead to the decomposition of the catalyst, which results in a significant reduction of the catalytic activity. Therefore, the preparation of homogeneous stabilized palladium nanoparticles catalysts has been widely studied. Stabilized palladium nanoparticles mainly use synthetic polymers. Cellulose microspheres, as a natural polymer material with low-cost and porous fiber network structure, are excellent carriers for stabilizing metal nanoparticles. Cellulose microspheres impregnated with palladium metal nanoparticles were carbonized to have a larger specific surface area and highly dispersed palladium nanoparticles, which exhibited excellent catalytic activity in the catalytic reduction of p-nitrophenol. In this work, the cellulose carbon-based microspheres palladium (Pd@CCM) catalysts were designed and characterized by SEM, TEM, EDS, XRD, FTIR, XPS, TGA, BET, and so on. Furthermore, the catalytic performance of Pd@CCM catalysts was investigated via p-nitrophenol reduction, which showed high catalytic activity. This catalyst also exhibited excellent catalytic performance in the Suzuki-Miyaura coupling reaction. Linking aromatic monomer and benzene through Suzuki-Miyaura coupling was presented as an effective route to obtaining biaryls, and the synthesis method is low-cost and simple. In addition, Pd@CCM showed desirable recyclability while maintaining its catalytic activity even after five recycles. This work is highly suggestive of the design and application of the heterogeneous catalyst.

Nanostructures embedded on porous materials for the catalytic reduction of nitrophenols: a concise review

Nanostructures embedded on porous materials for the catalytic reduction of nitrophenols: a concise review