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Highly Efficient Polydopamine-coated Poly(methyl methacrylate) Nanofiber Supported Platinum⁻nickel Bimetallic Catalyst for Formaldehyde Oxidation at Room Temperature.

ABSTRACT: We fabricated one fibrous-membrane type of flexible and lightweight supported catalyst via loading platinum-nickel nanoparticles (PtNi NPs) directly on the polydopamine-coated polymethylmethacrylate electrospun-fibers (PMMA@PDA). The polymer support with the PDA layer provided numerous active sites, leading to well-monodispersed and sized PtNi NPs on the nanofibers. Through the rational design of PtNi NPs, the resultant catalyst system exhibited 90% conversion for decomposing HCHO (10 ppm) at room temperature with only a low dosage (0.02 g), retaining the high activity for 100 hours. This superior catalytic performance stems from the formate oxidation, which was the key intermediate during HCHO decomposition, and was promoted by the existence of a sufficient Pt-OH-Ni interface in the PtNi NPs with an appropriate Pt/Ni ratio of 1:5. Such tailored Pt-based nanoparticles ideally work together with the polymer nanofibers as a support for catalytic reaction. Compared with classical catalysts, our system can handle a comparable efficiency with much lower air resistance and remarkably lower dosage. Furthermore, the membrane-like morphology provides easy handling and minimizes the leaching of catalyst nanoparticles.

SUBMITTER: He FG

PROVIDER: S-EPMC6523936 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Bimetallic nickel/manganese phosphate-carbon nanofiber electrocatalyst for the oxidation of formaldehyde in alkaline medium.

Project description:The development of earth-abundant transition metal-based catalysts, supported by a conductive carbonaceous matrix, has received great attention in the field of conversion of formaldehyde derivatives into toxic-free species. Herein, we report a comprehensive investigation of bimetallic electrocatalyst activity towards the electrooxidation of formaldehyde. The bimetallic phosphate catalyst is prepared by co-precipitation of Ni and Mn phosphate precursors using a simple reflux approach. Then the bimetallic catalyst is produced by mixing the Ni/Mn with carbon fibres (CNFs). The structural properties and crystallinity of the catalyst were investigated by using several techniques, such as scanning electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, and Brunauer Emmett-Teller theory. The system performance was studied under potentiostatic conditions. Some theoretical thermodynamic and kinetic models were applied to assess the system performance. Accordingly, key electrochemical parameters, including surface coverage (Γ) of active species, charge transfer rate (k s), diffusion coefficient of the formaldehyde (D), and catalytic rate constant (k cat) were calculated at Γ = 1.690 × 10-4 mmol cm-2, k s = 1.0800 s-1, D = 1.185 × 10-3 cm2 s-1 and k cat = 1.08 × 105 cm3 mol-1 s-1. These findings demonstrate the intrinsic electrocatalytic activity of formaldehyde electrooxidation on nickel/manganese phosphate- CNFs in alkaline medium.

| S-EPMC9292137 | biostudies-literature

Development of bimetallic nickel-based catalysts supported on activated carbon for green fuel production.

Project description:In this work, the catalytic deoxygenation of waste cooking oil (WCO) over acid-base bifunctional catalysts (NiLa, NiCe, NiFe, NiMn, NiZn, and NiW) supported on activated carbon (AC) was investigated. A high hydrocarbon yield above 60% with lower oxygenated species was found in the liquid product, with the product being selective toward n-(C15 + C17)-diesel fractions. The predominance of n-(C15 + C17) hydrocarbons with the concurrent production of CO and CO2, indicated that the deoxygenation pathway proceeded via decarbonylation and decarboxylation mechanisms. High deoxygenation activity with better n-(C15 + C17) selectivity over NiLa/AC exposed the great synergistic interaction between La and Ni, and the compatibility of the acid-base sites increased the removal of oxygenated species. The effect of La on the deoxygenation reaction performance was investigated and it was found that a high percentage of La species would be beneficial for the removal of C-O bonded species. The optimum deoxygenation activity of 88% hydrocarbon yield with 75% n-(C15 + C17) selectivity was obtained over 20% of La, which strongly evinced that La leads to a greater enhancement of the deoxygenation activity. The NiLa/AC reusability study showed consistent deoxygenation reactions with 80% hydrocarbon yield and 60% n-(C15 + C17) hydrocarbon selectivity within 6 runs.

| S-EPMC9057132 | biostudies-literature

Spatially Formed Tenacious Nickel-Supported Bimetallic Catalysts for CO<sub>2</sub> Methanation under Conventional and Induction Heating.

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Controlled Nutrient Delivery to Pancreatic Islets Using Polydopamine-Coated Mesoporous Silica Nanoparticles

Project description:In the present study, we designed a nanoscale platform for the sustained and controlled delivery of nutrients to pancreatic islets-upon transplantation. Our platform consists of a mesoporous silica nanoparticle (MSNP), loaded with glutamine (G), an essential amino acid required for islet survival and function, and capped with polydopamine (PD). To control the release of glutamine, various concentrations (0.5 - 2 mg/mL) of PD and incubation times (0.5 – 2 h) with MSNPs were investigated in terms of pharmacological properties and biological functions. After extensive testing, PD-G-MSNPs made using PD coating of 0.5 mg/mL incubated for 0.5 h resulted in the optimal platform to maintain the islet viability and functionality in vitro. Following syngeneic renal sub-capsule islet transplantation in STZ-diabetic mice, PD-G-MSNPs improved the engraftment of pancreatic islets as well as their function, resulting in re-establishment of glycemic control. Collectively, our data shows that PD-G-MSNPs can support transplanted islets by providing them with a controlled and sustained supply of nutrients.

2023-12-04 | GSE247020 | GEO

Microwave-Induced Chemotoxicity of Polydopamine-Coated Magnetic Nanocubes.

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| S-EPMC4581245 | biostudies-literature

An earth-abundant bimetallic catalyst coated metallic nanowire grown electrode with platinum-like pH-universal hydrogen evolution activity at high current density.

Project description:A self-supported and flexible current collector solely made of earth-abundant elements, NiCo layered double hydroxide (LDH) wrapped around Cu nanowires (Cu-Ws) grown on top of commercially available Cu mesh (Cu-m), outperforms the benchmark 40 wt% Pt/C in catalyzing the electrochemical hydrogen evolution reaction (HER). The Cu-m/Cu-W/NiCo-LDH cathode operates both in acidic and alkaline media exhibiting high turnover frequencies (TOF) at 30 mV (0.3 H2 s-1 in 1 M KOH and 0.32 H2 s-1 in 0.5 M H2SO4, respectively) and minimal overpotentials of 15 ± 6 mV in 1 M KOH and 27 ± 2 mV in 0.5 M H2SO4 at -10 mA cm-2. Cu-m/Cu-W/NiCo-LDH outperforms the activity of 40 wt% Pt/C that needs overpotentials of 22 and 18 mV in 1 M KOH and 0.5 M H2SO4, respectively. With a tremendous advantage over Pt/C in triggering proton reduction with fast kinetics, similar mass activity and pH-universality, the current collector demonstrates outstanding operational durability even at above -1 A cm-2. The high density of electronic states near the Fermi energy level of Cu-Ws is found to be a pivotal factor for efficient electron transfer to the NiCo-LDH catalyst. This class of self-supported electrodes is expected to trigger rapid progress in developing high performance energy conversion and storage devices.

| S-EPMC8152688 | biostudies-literature

Cellulose Nanofiber Composite with Bimetallic Zeolite Imidazole Framework for Electrochemical Supercapacitors.

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| S-EPMC7913791 | biostudies-literature

Development of Nickel- and Magnetite-Promoted Carbonized Cellulose Bead-Supported Bimetallic Pd-Pt Catalysts for Hydrogenation of Chlorate Ions in Aqueous Solution.

Project description:Cellulose grains were carbonized and applied as catalyst supports for nickel- and magnetite-promoted bimetallic palladium- and platinum-containing catalysts. The bimetallic spherical aggregates of Pd and Pt particles were created to enhance the synergistic effect among the precious metals during catalytic processes. As a first step, the cellulose bead-based supports were impregnated by nitrate salts of nickel and iron and carbonized at 973 K. After this step, the nickel was in an elemental state, while the iron was in a magnetite form in the corresponding supports. Then, Pd and Pt particles were deposited onto the supports and the catalyst surface; precious metal nanoparticles (10-20 nm) were clustered inside spherical aggregated particles 500-600 nm in size. The final bimetallic catalysts (i.e., Pd-Pt/CCB, Pd-Pt/Ni-CCB, and Pd-Pt/Fe3O4-CCB) were tested in hydrogenation of chlorate ions in the aqueous phase. For the nickel-promoted Pd-Pt catalyst, a >99% chlorate conversion was reached after 45 min at 80 °C. In contrast, the magnetite-promoted sample reached an 84.6% chlorate conversion after 3 h. Reuse tests were also carried out with the catalysts, and in the case of Pd-Pt/Ni-CCB after five cycles, the catalytic activity only decreased by ~7% which proves the stability of the system.

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Synthesis and catalytic performance of polydopamine supported metal nanoparticles.

Project description:Polydopamine (PDA) is an emerging nature-inspired biopolymer material that possesses many interesting properties including self-assembly and universal adhesion. PDA is also able to form coordination bonds with various metal ions, which can be reduced to metal nanoparticles (NPs) as a result of thermal annealing under protective environment. In this study, PDA has been utilized as a support material to synthesize Pt NPs in an aqueous solution at room temperature. The catalytic performance of the resulting PDA-Pt nanocomposite was evaluated using an electrochemical workstation which showed comparable activity to Pt/C material for hydrogen evolution reaction (HER). Furthermore, Cu, Ni, and Cu-Ni NPs supported on PDA were also obtained using this strategy with assistance of subsequent thermal annealing. The phase evolution of the NPs was studied by in-situ X-ray diffraction while the morphology of the nanoparticles was investigated using electron microscopic techniques. Preliminary results showed the NPs supported on PDA also possessed HER activity. This work demonstrates that PDA can be utilized as a potential support for synthesis of metal NPs that can be exploited in engineering applications such as catalysts.

| S-EPMC7319955 | biostudies-literature

An efficient catalytic degradation of trichloroethene in a percarbonate system catalyzed by ultra-fine heterogeneous zeolite supported zero valent iron-nickel bimetallic composite.

Project description:Zeolite supported nano iron-nickel bimetallic composite (Z-nZVI-Ni) was prepared using a liquid-phase reduction process. The corresponding surface morphologies and physico-chemical properties of the Z-nZVI-Ni composite were determined using scanning electron microscopy (SEM), transmission electron microscopy (TEM), Energy dispersive X-ray spectra (EDS), Brunauer Emmett Teller (BET) adsorption, wide angle X-ray diffractometry (WA-XRD), and Fourier transform infrared spectroscopy (FTIR). The results indicated high dispersion of iron and nickel nano particles on the zeolite sheet with an enhanced surface area. Complete destruction of trichloroethene (TCE) and efficient removal of total organic carbon (TOC) were observed by using Z-nZVI-Ni as a heterogeneous catalyst for a Fenton-like oxidation process employing sodium percarbonate (SPC) as an oxidant. The electron spin resonance (ESR) of Z-nZVI-Ni verified the generation and intensity of hydroxyl radicals (OH•). The quantification of OH• elucidated by using p-chlorobenzoic acid, a probe indicator, confirmed the higher intensity of OH•. The transformation products were identified using GC-MS. The slow iron and nickel leaching offered higher stability and better catalytic activity of Z-nZVI-Ni, demonstrating its prospective long term applications in groundwater for TCE degradation.

| S-EPMC5665389 | biostudies-literature

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