Browse
Submit Data
Databases
API
Help

Dataset Information

30 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Fine platinum nanoparticles supported on a porous ceramic membrane as efficient catalysts for the removal of benzene.

ABSTRACT: It would be desirable to remove volatile organic compounds (VOCs) while we eliminate the dusts using silicon carbide (SiC)-based porous ceramics from the hot gases. Aiming at functionalizing SiC-based porous ceramics with catalytic capability, we herein report a facile strategy to integrate high efficient catalysts into the porous SiC substrates for the VOC removal. We demonstrate an aqueous salt method for uniformly distributing fine platinum (Pt) particles on the alumina (Al2O3) layers, which are pre-coated on the SiC substrates as supports for VOC catalysts. We confirm that at a Pt mass loading as low as 0.176% and a weight hourly space velocity of 6000?mL?g-1 h-1, the as-prepared Pt/SiC@Al2O3 catalysts can convert 90% benzene at a temperature of ca. 215?°C. The results suggest a promising way to design ceramics-based bi-functional materials for simultaneously eliminating dusts and harmful VOCs from various hot gases.

SUBMITTER: Liu H

PROVIDER: S-EPMC5707434 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Fine platinum nanoparticles supported on a porous ceramic membrane as efficient catalysts for the removal of benzene.

Liu Hui H Li Chengyin C Ren Xiaoyong X Liu Kaiqi K Yang Jun J

Scientific reports 20171129 1

It would be desirable to remove volatile organic compounds (VOCs) while we eliminate the dusts using silicon carbide (SiC)-based porous ceramics from the hot gases. Aiming at functionalizing SiC-based porous ceramics with catalytic capability, we herein report a facile strategy to integrate high efficient catalysts into the porous SiC substrates for the VOC removal. We demonstrate an aqueous salt method for uniformly distributing fine platinum (Pt) particles on the alumina (Al2O3 ...[more]

PMID: 29185476

Similar Datasets

Efficient and Environmentally Friendly Synthesis of AlFe-PILC-Supported MnCe Catalysts for Benzene Combustion.

Project description:An efficient and environmentally friendly synthesis of AlFe-pillared clay (AlFe-PILC)-supported MnCe catalysts was explored. Mixed AlFe pillaring agents were prepared by a one-step method using Locron L and ferric nitrate solutions at a high temperature and high pressure. Montmorillonite was treated with the AlFe pillaring agents to synthesize AlFe-PILC. MnO x and CeO2 with different Mn/Ce atomic ratios were loaded onto the AlFe-PILC support by an impregnation method. The catalysts were characterized using X-ray diffraction, N2 adsorption, and high-resolution transmission electron microscopy-energy dispersive spectrometry and were tested for the catalytic combustion of benzene and temperature-programmed surface reaction using a microreactor. Compared to conventional methods, this method is simpler and less costly and results in a larger specific surface area, pore volume, and basal spacing, with the ability to control the structure of the catalytic materials. MnCe(6:1)/AlFe-PILC has the highest catalytic activity and can completely degrade benzene (600 ppm in air) at 250 °C. The activity of the catalyst is stable, and no obvious deactivation is observed at 230 °C after 1000 continuous hours. The catalyst is resistant to water and Cl-poisoning. The amount of CeO2 added is critical to the dispersion of MnO x on the support and the creation of optimum number of oxygen vacancy defect sites for the benzene oxidation reaction. The AlFe-PILC-supported MnCe catalyst is a promising porous material; the support structure, proper dispersion of active species, and addition of Ce are essential for achieving complete degradation of organic toxic chemicals at relatively low temperatures.

| S-EPMC6641775 | biostudies-literature

Tying Covalent Organic Frameworks through Alkene Metathesis and Supported Platinum as Efficient Catalysts for Hydrosilylation.

Project description:Recently there has been a great interest in covalent organic frameworks due to their fascinating properties. Current approaches to improve their hydrolytic stability mainly rely on the transformation of the dynamic bonds into strong and irreversible bonds, but these approaches also reduce the versatility of the frameworks. Herein, we would like to demonstrate a solution to this dilemma by forming hierarchical bonds through olefin metathesis to produce highly stable COFs. Our approach allows unprecedented opportunities for post-modification of the inner space through the dynamic imine bonds while maintaining the integrity of the framework. Specifically, we demonstrate an amorphous-to-crystalline transformation. In addition, the porosity can be enhanced by up to 70% after full removal of the amine subunits. Overall, our work provides a new direction for the generation of highly stable while still versatile COFs. Meanwhile, platinum(II) complexes can be supported on BHU-2 (Pt@BHU-2) or BHU-2-Oxidate(Pt@BHU-2-Oxidate) as efficient catalysts for hydrosilylation.

| S-EPMC8915182 | biostudies-literature

Ultrafine platinum nanoparticles supported on N,S-codoped porous carbon nanofibers as efficient multifunctional materials for noticeable oxygen reduction reaction and water splitting performance.

Project description:The design of highly active, stable and durable platinum-based electrocatalysts towards the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and hydrogen adsorption has a high and urgent demand in fuel cells, water splitting and hydrogen storage. Herein, ultrafine platinum nanoparticles (Pt NPs) supported on N,S-codoped porous carbon nanofibers (Pt-N,S-pCNFs) hybrids were prepared through the electrospinning method coupled with hydrothermal and carbonation processes. The ultrafine Pt NPs are sufficiently dispersed and loaded on pCNFs and codoped with N and S, which can improve oxygen adsorption, afford more active sites, and greatly enhance electron mobility. The Pt-N,S-pCNFs hybrid achieves excellent activity and stability for ORR with ∼70 mV positive shift of onset potential compared to the commercial Pt/C-20 wt% electrocatalyst. The long-term catalytic durability with 89.5% current retention after a 10 000 s test indicates its remarkable ORR behavior. Pt-N,S-pCNFs also exhibits excellent HER and OER performance, and can be used as an efficient catalyst for water splitting. In addition, Pt-N,S-pCNFs exhibits an excellent hydrogen storage capacity of 0.76 wt% at 20 °C and 10 MPa. This work provides novel design strategies for the development of multifunctional materials as high-performance ORR catalysts, water splitting electrocatalysts and hydrogen storage materials.

| S-EPMC9417137 | biostudies-literature

Novel porous ceramic sheet supported metal reactors for continuous-flow catalysis.

Project description:A novel porous ceramic sheet supported nickel particles reactor was obtained by an in-situ preparation method. This reactor was then used to investigate continuous-flow catalysis of nitroaromatic compounds and methyl orange. The details of the structure and morphology were characterized by XRD, SEM, XPS, Raman, element mapping, mercury intrusion method and Archimedes principle. The porous ceramic sheet supported Ni particles reactor exhibited excellent catalytic performance in the catalytic reduction of p-nitrophenol and methyl orange by sodium borohydride at room temperature. Both the conversion of p-nitrophenol (5 mM) and methyl orange (0.3 mM) reached nearly 100% at the injection speed of 2.67 mL·min-1. In addition, it maintained conversions of 100% after 10 recycling time since the porous ceramic sheet could reduce the aggregation for Ni particles. Furthermore, the chemisorbed oxygen, and the strong interaction between Ni and porous ceramic sheet resulted in a highly efficient, recoverable, and cost-effective multifunctional reactor. All of these advantages present new opportunities to be implemented in the field of waste water treatment and environmental toxicology. Ultimately, the porous ceramic sheet could also support other metal nanomaterial, and used in other fields of environmental catalysis.

| S-EPMC7792823 | biostudies-literature

Bimetallic ZIF-Derived Co/N-Codoped Porous Carbon Supported Ruthenium Catalysts for Highly Efficient Hydrogen Evolution Reaction.

Project description:Exploring the economical, powerful, and durable electrocatalysts for hydrogen evolution reaction (HER) is highly required for practical application. Herein, nanoclusters-decorated ruthenium, cobalt nanoparticles, and nitrogen codoped porous carbon (Ru-pCo@NC) are prepared with bimetallic zeolite imidazole frameworks (ZnCo-ZIF) as the precursor. Thus, the prepared Ru-pCo@NC catalyst with a low Ru loading of 3.13 wt% exhibits impressive HER catalytic behavior in 1 M KOH, with an overpotential of only 30 mV at the current density of 10 mA cm-2, Tafel slope as low as 32.1 mV dec-1, and superior stability for long-time running with a commercial 20 wt% Pt/C. The excellent electrocatalytic properties are primarily by virtue of the highly specific surface area and porosity of carbon support, uniformly dispersed Ru active species, and rapid reaction kinetics of the interaction between Ru and O.

| S-EPMC8148513 | biostudies-literature

MWCNT-Supported PVP-Capped Pd Nanoparticles as Efficient Catalysts for the Dehydrogenation of Formic Acid.

Project description:Various carbon materials were used as support of polyvinylpyrrolidone (PVP)-capped Pd nanoparticles for the synthesis of catalysts for the production of hydrogen from formic acid dehydrogenation reaction. Among investigated, MWCNT-supported catalysts were the most promising, with a TOF of 1430 h-1 at 80°C. The presence of PVP was shown to play a positive role by increasing the hydrophilicity of the materials and enhancing the interface contact between the reactant molecules and the catalytic active sites.

| S-EPMC7199183 | biostudies-literature

Nitrogen-Rich Porous Organic Polymers with Supported Ag Nanoparticles for Efficient CO2 Conversion.

Project description:As CO2 emissions increase and the global climate deteriorates, converting CO2 into valuable chemicals has become a topic of wide concern. The development of multifunctional catalysts for efficient CO2 conversion remains a major challenge. Herein, two porous organic polymers (NPOPs) functionalized with covalent triazine and triazole N-heterocycles are synthesized through the copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction. The NPOPs have an abundant microporous content and high specific surface area, which confer them excellent CO2 affinities with a CO2 adsorption capacity of 84.0 mg g-1 and 63.7 mg g-1, respectively, at 273 K and 0.1 MPa. After wet impregnation and in situ reductions, Ag nanoparticles were supported in the NPOPs to obtain Ag@NPOPs with high dispersion and small particle size. The Ag@NPOPs were applied to high-value conversion reactions of CO2 with propargylic amines and terminal alkynes under mild reaction conditions. The carboxylative cyclization transformation of propargylic amine into 2-oxazolidinone and the carboxylation transformation of terminal alkynes into phenylpropiolic acid had the highest TOF values of 1125.1 and 90.9 h-1, respectively. The Ag@NPOP-1 was recycled and used five times without any significant decrease in catalytic activity, showing excellent catalytic stability and durability.

| S-EPMC9501012 | biostudies-literature

Planar oxide supported rhodium nanoparticles as model catalysts.

Project description:C(2)H(4)/CO/H(2) reaction is investigated on Rh/SiO(2) model catalyst surfaces. Kinetic reactivity and infrared spectroscopic measurements are investigated as a function of Rh particle size under near atmospheric reaction conditions. Results show that propionaldehyde turnover frequency (TOF) (CO insertion pathway) exhibits a maximum activity near <d(p)> = 2.5 nm. Polarization modulation infrared reflection absorption spectroscopy under CO and reaction (C(2)H(4)/CO/H(2)) conditions indicate the presence of Rh carbonyl species (Rh(CO)(2), Rh(CO)H) on small Rh particles, whereas larger particles appear resistant to dispersion and carbonyl formation. Combined these observations suggest the observed particle size dependence for propionaldehyde production via CO insertion is driven by two factors: (i) an increase in propionaldehyde formation on undercoordinated Rh sites and (ii) creation of carbonyl hydride species (Rh(CO)H)) on smaller Rh particles, whose presence correlates with the lower activity for propionaldehyde formation for <d(p)> < 2.5 nm.

| S-EPMC3024686 | biostudies-literature

Ultra-fine platinum species supported on niobium pentoxide for CO oxidation.

Project description:Platinum oxide supported on a Lewis acid niobium oxide (Nb2O5) support has been used for various heterogeneous and homogeneous catalysts. In this work, we used urea as a precipitating agent to obtain crystallized Nb2O5 with high surface area via a hydrothermal route. Nb2O5-supported Pt catalysts were subsequently synthesized via an incipient wetness impregnation approach. Multiple characterizations including X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and nitrogen adsorption/desorption confirmed the identical structural and textural properties of the Nb2O5 support before and after the impregnation process. Furthermore, the X-ray absorption fine structure technique (XAFS) results with related data analysis indicate that the platinum species in the fresh and H2-pretreated samples were in the form of single atoms or ultrafine clusters. In addition, the decrease in coordination number (CN) of the first-shell Pt-O bond, as well as the formation of Pt-Pt contribution with very low CN, after H2-pretreatment was verified, which corresponds to the decrease of oxidation state for Pt species on the surface of supports. Thus, the ultrafine-clustered metallic Pt species are considered to be more active than the oxidized Pt single ions. The current results will be of great significance in controllable synthesis of active Pt-based catalysts for other catalytic oxidation reactions.

| S-EPMC9050684 | biostudies-literature

Oxidative strong metal-support interactions (OMSI) of supported platinum-group metal catalysts.

Project description:Supported platinum-group metal (PGM) catalysts are widely used in many important industrial processes. Metal-support interaction is of great importance in tailoring their catalytic performance. Here, we report the first example of oxidative strong metal-support interactions (OMSIs) between PGM and hydroxyapatite (HAP) which can be extended to PGM and ZnO. It occurred under high-temperature oxidation conditions accompanied by the encapsulation of PGM by HAP and electron transfer between PGM and HAP. With this OMSI, the aggregation and leaching of PGMs were significantly inhibited, resulting in an excellent catalytic stability and much improved reusability of supported Pt and Pd catalysts, respectively. This is the first time to find that PGMs can manifest OMSI which benefits the stabilization of PGM catalysts under oxidative reaction conditions. This new type of SMSI not only contributed to a deeper understanding of SMSI but also provided a new way to develop new stable PGM catalysts.

| S-EPMC6115625 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data