Search Results (466)

To ensure the sustainable use of limited resources, it is essential to establish selective and efficient recycling technologies for platinum group metals (PGMs). This study focused on the selective precipitation-based separation of Pt(IV) from hydrochloric acid (HCl) solutions in the presence of various metal ions, using trans-1,4-bis(aminomethyl)cyclohexane (BACT) as a precipitating agent. By using BACT, we succeeded in the selective separation of Pt(IV) by precipitation from HCl solutions containing Pd(II) and Rh(III). Notably, selective and efficient recovery of Pt(IV) was accomplished across various HCl concentrations, with a small amount of BACT and within a short shaking time. To evaluate the practical applicability of the method, Pt(IV) was recovered and purified from the HCl leachate of spent automotive exhaust gas purification catalysts using BACT. As a result, a high Pt recovery of 95.6% and a high purity of 99.3% were achieved. Although Pt(IV) was recovered as a precipitate containing BACT, it was found that Pt black could be readily obtained by dissolving the precipitate in HCl solution followed by reduction with sodium borohydride. Detailed structural analysis of the Pt(IV)-containing precipitate revealed that it is an ionic crystal composed of [PtCl₆]²⁻ and protonated BACT. The selective formation of this ionic crystal in HCl solution, along with its stability under such conditions, is the key to the selective recovery of Pt(IV) using BACT. Full article

Fe-doped BiOBr nanomaterials with varying Fe concentrations were synthesized using a solvothermal method. Paracetamol (APAP) was selected as the target pollutant to evaluate the visible-light-driven peroxydisulfate (PDS) activation performance of the prepared catalysts. Among all samples, 5% Fe-doped BiOBr (5% Fe-BOB) exhibited the highest catalytic efficiency, which can completely degrade APAP in 30 min under visible light irradiation. The degradation kinetics of APAP, PDS consumption, and the dominant reactive species in the 5% Fe-BOB/PDS/visible light system were systematically investigated. Results revealed that both photocatalyst dosage and PDS concentration significantly influenced activation efficiency. The primary active species responsible for APAP degradation were identified as photogenerated holes (h⁺) and singlet oxygen (¹O₂). Furthermore, cycling tests and control experiments confirmed that the 5% Fe-BOB/PDS/visible light system maintained high stability and effectively degraded APAP across a wide pH range. This work provides an efficient and stable photocatalytic system for pharmaceutical wastewater treatment through PDS-based advanced oxidation processes. Full article

Hexavalent chromium [Cr(VI)] is a hazardous environmental contaminant, and palladium nanoparticles (PdNPs) have shown promise as catalysts for its reduction. This study explores the primary factor influencing the catalytic performance of PdNPs in Cr(VI) reduction by investigating the crystal structure and composition of PdNPs in fungal-based catalysts. Five Pd-loaded catalysts were synthesized by treating fungal biomass with different chemical reagents, resulting in varying Pd(0) contents. The nanoparticle morphology, chemical states, and functional group interactions during Pd adsorption and reduction were investigated using multiple analytical techniques. The results showed that fungal hyphae remained structurally intact throughout the treatment process. PdNPs smaller than 2 nm were observed, with both Pd(0) and PdO present. The proportion of Pd(0) ranged from 6.4% to 37.2%, depending on the chemical reagent used. In addition, functional groups such as phosphate, amine, hydroxyl, and carboxyl were found to play key roles in palladium binding, underscoring the importance of surface chemistry in the adsorption and reduction process. A strong positive correlation was observed between the Pd(0) content and catalytic activity. Notably, the NCPdSF sample (palladium-loaded biomass treated with sodium formate) exhibited the highest Pd(0) content of 59.2% and achieved the most effective Cr(VI) reduction. These results suggest that Pd(0) content is a key determinant of catalytic efficiency in Cr(VI) reduction and that optimizing chemical treatments to enhance Pd(0) levels can substantially improve catalyst performance. Full article

In this work, the effect of the palladium precursor on the Oxygen Reduction Reaction (ORR) performance of lignin-based electrospun carbon fibers was studied. The fibers were spun from a lignin-ethanol solution free of any binder, where different Pd salts were added at two concentration levels. The system implemented to perform the spinning was a coaxial setup in which the internal flow contains the precursor dispersion with the metallic precursor, and ethanol was used as external flow to help fiber formation and prevent drying before generating the Taylor cone. The obtained cloths were thermostabilized in air at 200 °C and carbonized in nitrogen at 900 °C. The resulting carbon fibers were characterized by physicochemical and electrochemical techniques. The palladium precursor significantly affects nanoparticle distribution and size, fiber diameter, pore distribution, surface area and electrochemical behavior. The fibers prepared with palladium acetylacetonate at high Pd loading and carbonized at 900 °C under a CO₂ atmosphere showed high mechanical stability and the best ORR activity, showing near total selectivity towards the 4-electron path. These features are comparable to those of the commercial Pt/C catalyst but much lower metal loading (10.6 wt.% vs. 20 wt.%). The most promising fibers have been evaluated as cathodes in a zinc–air battery, delivering astonishing stability results that surpassed the performance of commercial Pt/C materials in both charging and discharging processes. Full article

A separable bamboo-like carbon nanotube-based catalyst was prepared by the spherfication method using sodium alginate and nickel. The spheres were carbonized and then decorated with palladium nanoparticles before they were tested in nitrobenzene hydrogenation. The test was repeated with five different commonly used solvents (methanol, ethanol, isopropanol, tetrahydrofuran, and acetonitrile). According to the results, polar solvents showed a significantly higher aniline yield than the more apolar solvents and exceptional results were reported for ethanol (~100%). The catalyst was reused two more times (four hours each) to check the Pd leaching where the spheres kept their shape (despite the high mechanical friction caused by the mixer) and only a relatively low Pd amount was lost (5.48 rel.%). The catalyst was easily retrievable. Full article

The importance and challenges of ethylene detection based on combustion-type low-cost commercial sensors for agricultural and industrial applications are well-established. This work summarizes the significant progress in ethylene detection based on an innovative Gas Metal Oxide Semiconductor (GMOS) sensor and a new catalytic composition of metallic nanoparticles. The paper presents a study on ethylene and ethanol sensing using a miniature catalytic sensor fabricated by Complementary Metal Oxide Semiconductor–Silicon-on-Insulator–Micro-Electro-Mechanical System (CMOS-SOI-MEMS) technology. The GMOS performance with bimetallic palladium–platinum (Pd-Pt) and monometallic palladium (Pd) and platinum (Pt) catalysts is compared. The synergetic effect of the Pd-Pt catalyst is observed, which is expressed in the shift of combustion reaction ignition to lower catalyst temperatures as well as increased sensitivity compared to monometallic components. The optimal catalysts and their temperature regimes for low and high ethylene concentrations are chosen, resulting in lower power consumption by the sensor. Full article

Hydrogen peroxide (H₂O₂) is an important industrial chemical that is widely applied in many areas. The direct synthesis of H₂O₂ from H₂ and O₂ has proved to be a green and economic pathway. Pd-based bimetallic catalysts, due to their superior catalytic performances in this reaction, have attracted intensive attention. Herein, Tetrakis(hydroxymethyl)phosphonium chloride (THPC) was adopted as the protective ligand to immobilize Pd-Au alloy nanoparticles onto activated carbon (AC). The varied Pd/Au molar ratios demonstrated homogeneously distributed Pd-Au nanoalloys with average particle sizes ranging from 3.51 to 5.75 nm. The optimal ratio was observed over the Pd₃Au₁/AC-THPC catalyst with a maximum H₂O₂ productivity of 165 mol/(kg_Pd·h) and selectivity of 82.3% under ambient pressure. The relationship between the electronic structure and catalytic activity indicated Pd⁰ was the active site, while the presence of Au inhibited H₂O₂ degradation rate. This research could help in the design efficient bimetallic catalysts for the direct synthesis of H₂O₂. Full article

This work reports the synthesis of two monometallic catalysts, Cu/Al₂O_3, and Pd/Al₂O₃, using a green approach based on Mexican oregano (Lippia graveolens), a common food condiment. Its extract has been largely overlooked as a high-technology reactive for synthesizing catalysts, metallic or oxide nanoparticles, unlike other green leaf plants. The green synthesis was compared with a conventional catalyst synthesis methodology using commercial chemical reducing agents. Oregano extract shows promise for novel applications extending beyond its culinary use, valorizing it as a chemical reducer to produce catalysts. Thus, this kind of application could significantly elevate the value of oregano, empowering communities that rely on its cultivation for economic benefit and transforming the plant from a low-profit agro-industrial product to a high-added-value crop. The reduction kinetics involved in the formation of nanoparticles were monitored up to the first stage of nucleation and a first-order model adequately described the data. Activation energy analysis showed that the chemical reaction mechanism has a dominant role in controlling the reaction, compared to mass transfer effects. Notoriously, the Pd/Al₂O₃ green synthesis catalyst showed the smallest mean particle size (4.85 ± 1.30 nm). These findings underscore the potential of green synthesis as an economically viable and environmentally friendly alternative for producing catalysts. Concerning the 5-hydroxymethyl-2-furancarboxylic acid (HMFCA) as a biomass-derived molecule, its oxidation with H₂O₂ using both Pd/Al₂O₃ catalysts (by green and chemical synthesis methods) exhibited significantly higher selectivity toward 2,5-diformylfuran (DFF) compared to Cu/Al₂O₃ catalysts, suggesting a possible inhibitory effect. Full article

Magnesium-based alloys, known for their high hydrogen storage capacity, suffer from sluggish kinetics and high activation energy barriers. It can be further optimized through synergistic combinations with metal hydrides. This study aims to address these limitations by investigating the hydrogen sorption properties of AZ31 magnesium alloy combined with different compositions of WS2 nanotubes (NTs) and Pd. The materials AZ31, WS2 (tungsten disulfide) NTs, and Pd were pre-processed via the mechanical ball milling process. Field emission-scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) were employed to investigate the composite morphology and confirm the nanotubular structure of WS₂. This work is among the first to explore the synergistic catalytic effects of WS₂ nanotubes and Pd on the hydrogenation/dehydrogenation behavior of AZ31 alloys. The composite with 8 wt.% WS₂ NT/Pd demonstrated the fastest hydrogen sorption kinetics and a significant reduction in activation energy, from 123.25 kJ/mol to 104.58 kJ/mol. These results highlight the enhanced dehydrogenation performance of AZ31 through catalyst inclusion, offering a promising approach to improve hydrogen storage materials. These findings highlight the potential of combining inorganic NTs and transition metals as effective catalysts to enhance the hydrogen storage performance. This research paves the way for developing advanced hydrogen storage materials with improved performance, contributing to a sustainable energy future. Full article

Supported Pd-based catalysts have been widely applied in the hydrogenation of specific functional groups. Recent trends have focused on employing Pd-based heterogeneous catalysts supported on inorganic nanotubes, wherein inner surface functionalization modulates both palladium nanoparticle (Pd-NP) dispersion and the interaction between reactants and the catalyst surface, thereby influencing catalytic properties. This study aims to develop a catalytic system using amine-lumened halloysite nanotubes immobilizing Pd-NPs (Pd/HNTA) as catalysts for hydrogenation reactions. The formation of Pd-NPs within the organo-functionalized lumen—modified by 3-aminopropyltrimethoxysilane—is confirmed by transmission electron microscopy (TEM) imaging, which reveals a particle size of 2.2 ± 0.4 nm. For comparison, Pd-NPs supported on pristine halloysite (Pd/HNTP) were used as control catalysts, displaying a metal particle size of 2.8 ± 0.8 nm and thereby demonstrating the effect of organic functionalization on the halloysite nanotubes. Both catalysts were employed in the hydrogenation of furfural (FUR) and nitrobenzene (NB) as model reactions. Pd/HNTA demonstrated superior catalytic performance for both substrates, with TOF values of 880 h⁻¹ for FUR and 946 h⁻¹ for NB, and selectivities exceeding 98% for tetrahydrofurfuryl alcohol (THFOH) and aniline (AN), respectively. However, recyclability studies displayed that Pd/HNTA was deactivated at the 10 catalytic cycles during the hydrogenation of FUR, whereas, in the hydrogenation of NB, 5 catalytic cycles were achieved with maximum conversion and selectivity at 360 min. These results revealed that the liquid-phase environment plays a pivotal role in catalyst stability. In the hydrogenation of NB, the coproduction of H₂O adversely affects the interaction between the Pd particles and the inner amine-modified surface, increasing the deactivation of the catalyst with reuse. Thus, the Pd/HNTA catalyst holds significant promise for the development of noble-metal-based catalysts and their application in the transformation of other reducible organic functional groups via hydrogenation reaction. Full article

The electrocatalytic hydrogenation (ECH) of biomass-derived phenolic compounds is a promising approach to the production of value-added chemicals and biofuels in a sustainable way under moderate reaction conditions. This study provides a comprehensive comparison of electrochemical and thermochemical hydrogenation processes, highlighting their relative advantages in terms of energy efficiency, product selectivity, and environmental impact. Several electrocatalysts (Pt, Pd, Rh, Ru), membranes (Nafion, Fumasep, GO-based PEMs), and reactor configurations are tested for the selective conversion of model compounds such as phenol, guaiacol, furfural, and levulinic acid. The contributions made by the electrode material, electrolyte composition, membrane nature, and reaction conditions are critically evaluated in relation to Faradaic efficiency, conversion rates, and product selectivity. The enhancement in the performance achieved by a new catalyst architecture is emphasized, such as MOF-based systems and bimetallic/trimetallic catalysts. In addition, a demonstration of graphite-based membranes and membrane-separated slurry reactors (SSERs) is provided, for enhanced ion transport and reaction control. The results illustrate the potential of using ECH as a low-carbon, scalable, and tunable method for the upgrading of biomass. This study offers valuable insights and guidelines for the rational design of next-generation electrocatalytic systems toward green chemical synthesis and emphasizes promising perspectives for the strategic development of electrochemical technologies in the pathway of a sustainable energy economy. Full article

Platinum- and/or palladium-containing silica-based supports were applied for the selective catalytic reduction of NO_x with hydrogen (H₂-SCR-DeNO_x). To obtain enhanced activity and N₂ selectivity below 150 °C, we varied the type and loading of noble metals (Pt and Pd both individually and paired, 0.1–1.0 wt.-%), silica-containing supports (ZrO₂/SiO₂, ZrO₂/SiO₂/Al₂O₃, Al₂O₃/SiO₂/TiO₂), as well as the H₂ concentration in the feed (2000–4000 ppm). All of these contributed to enhancing N₂ selectivity during H₂-SCR-DeNO_x over the (0.5 wt.-%)Pt/Pd/ZrO₂/SiO₂ catalyst in the presence of 10 vol.-% of O₂. H₂ was completely consumed at 150 °C. A comparison of the catalytic results obtained during H₂-SCR-DeNO_x,(H₂-)NH₃-SCR-DeNO_x, as well as stop-flow H₂-SCR-DeNO_x and temperature-programmed studies, revealed that in the temperature range between 150 and 250 °C, the continuously coupled or overlaying mechanism of NO reduction by hydrogen and ammonia based on NH₃ formation at lower temperatures, which is temporarily stored at the acid sites of the support and desorbed in this temperature range, could be postulated. Full article

This study explores the selective hydrogenation of cinnamaldehyde using a series of metal catalysts supported on reduced graphene oxide (rGO) and conventional activated carbon (AC). Catalysts based on Pt, Pd, Rh, Ru, and Co were synthesized with controlled metal loading and characterized by XRD, SEM-EDS, XRF, and TEM. Among all tested materials, Pd supported on rGO synthesized via the Tour method (Pd/rTOGO) exhibited the highest catalytic activity, achieving 62% conversion of cinnamaldehyde and superior selectivity toward hydrocinnamaldehyde (HCAL). The support material had a significant influence on performance, especially for Pd catalysts, where 2D rGO outperformed 3D AC in both conversion and selectivity. In contrast, other metals (Pt, Rh, Ru, Co) showed only modest activity and limited selectivity tuning via support choice. Notably, GC-MS analysis revealed the formation of a previously underreported side product, 3-isopropoxy-propan-1-yl benzene (ether), likely formed via reductive etherification in isopropanol. The combined kinetic and selectivity data enabled the proposal of reaction pathways, including rapid transformation of cinnamylalcohol (COL) to hydrocinnamal alcohol (HCOL) and HCAL to ether. These findings emphasize the importance of support structure and surface functionality, particularly in 2D carbon materials, for designing efficient and selective hydrogenation catalysts. Full article

The electrochemical CO₂ reduction reaction (eCO₂RR), driven by renewable energy, represents a promising strategy for mitigating atmospheric CO₂ levels while generating valuable fuels and chemicals. Its practical implementation hinges on the development of highly efficient electrocatalysts. In this study, a novel dual-metal atomic catalyst (DAC), composed of niobium and palladium single atoms anchored on a ferroelectric α-In₂Se₃ monolayer (Nb-Pd@In₂Se₃), is proposed based on density functional theory (DFT) calculations. The investigation encompassed analyses of structural and electronic characteristics, CO₂ adsorption configurations, transition-state energetics, and Gibbs free energy changes during the eCO₂RR process, elucidating a synergistic catalytic mechanism. The Nb-Pd@In₂Se₃ DAC system demonstrates enhanced CO₂ activation compared to single-atom counterparts, which is attributed to the complementary roles of Nb and Pd sites. Specifically, Nb atoms primarily drive carbon reduction, while neighboring Pd atoms facilitate oxygen species removal through proton-coupled electron transfer. This dual-site interaction lowers the overall reaction barrier, promoting efficient CO₂ conversion. Notably, the polarization switching of the In₂Se₃ substrate dynamically modulates energy barriers and reaction pathways, thereby influencing product selectivity. Our work provides theoretical guidance for designing ferroelectric-supported DACs for the eCO₂RR. Full article

Carbon monoxide (CO) is an important air pollutant generated from the incomplete combustion of fossil fuels, particularly in industrial processes such as iron and steel smelting, power generation, and waste incineration, posing environmental challenges that demand effective removal strategies. Recent advances in noble metal catalysts for catalytic oxidation of CO, particularly Pt-, Pd-, and Rh-based systems, have been extensively studied. However, there is still a lack of systematic review on noble metal-based catalytic oxidation of CO, especially regarding the effects of different active components of the catalysts and the mechanism of sulfur resistance. Based on extensive research and literature findings, this study comprehensively concluded the advances in noble metal-based catalytic oxidation of CO. The effects of preparation methods, supports, and physicochemical properties on the catalytic performance of CO were explored. In addition, the mechanism of the catalytic oxidation of CO were further summarized. Furthermore, given the prevalence of SO₂ in the flue gas, the mechanism of sulfur poisoning deactivation of catalysts and the anti-sulfur strategies were further reviewed. Exploration of new supporting materials, catalyst surface reconstruction, doping modification, and other catalyst design strategies demonstrate potential in improving sulfur resistance and catalytic efficiency. This study provides valuable insights into the design and optimization of noble metal-based catalysts for the catalytic oxidation of CO. Full article