Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Fabrication of Yolk-Shell Cu@C Nanocomposites as High-Performance Catalysts in Oxidative Carbonylation of Methanol to Dimethyl Carbonate.

ABSTRACT: A facile way was developed to fabricate yolk-shell composites with tunable Cu cores encapsulated within hollow carbon spheres (Cu@C) with an average diameter about 210 nm and cavity size about 80 nm. During pyrolysis, the confined nanospace of hollow cavity ensures that the nucleation-and-growth process of Cu nanocrystals take place exclusively inside the cavities. The size of Cu cores can be easily tuned from 30 to 55 nm by varying the copper salt concentration. By deliberately creating shell porosity through KOH chemical activation, at an optimized KOH/HCS mass ratio of 1/4, the catalytic performance for the oxidative carbonylation of methanol to dimethyl carbonate (DMC) of the activated sample is enhanced remarkably with TOF up to 8.6 h-1 at methanol conversion of 17.1%. The activated yolk-shell catalyst shows promising catalytic properties involving the reusability with slight loss of catalytic activity and negligible leaching of activated components even after seven recycles, which is beneficial to the implementation of clean production for the eco-friendly chemical DMC thoroughly.

SUBMITTER: Wang J

PROVIDER: S-EPMC5548704 | biostudies-other | 2017 Aug

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Similar Datasets

CO2 Hydrogenation to Methanol over Mesoporous SiO2-Coated Cu-Based Catalysts

Project description: Not available

| S-EPMC11342343 | biostudies-literature

Design and Synthesis of Cu@CuS Yolk-Shell Structures with Enhanced Photocatalytic Activity.

Project description:Non-spherical Cu@CuS yolk-shell structures are successfully obtained using Cu2O cube templates in a process combining rapid surface sulfidation followed by disproportionation of the Cu2O core upon treatment with a hydrochloric acid solution. By employing the above method, Cu@CuS yolk-shell structures with different morphologies, including octahedral, truncated octahedral, and cuboctahedral shapes, can be synthesized. The void space within the hollow structures provides a unique confined space, where the metallic copper present in the core of a shell can be protected from agglomeration and oxidation. Furthermore, the presence of metal copper in these hollow structures contributes to improvement in the photocatalytic properties of these materials. The application of these Cu@CuS structures indeed shows clearly improved photocatalytic performance.

| S-EPMC6199031 | biostudies-literature

Structure sensitivity of Cu and CuZn catalysts relevant to industrial methanol synthesis.

Project description:For decades it has been debated whether the conversion of synthesis gas to methanol over copper catalysts is sensitive or insensitive to the structure of the copper surface. Here we have systematically investigated the effect of the copper particle size in the range where changes in surface structure occur, that is, below 10?nm, for catalysts with and without zinc promotor at industrially relevant conditions for methanol synthesis. Regardless of the presence or absence of a zinc promotor in the form of zinc oxide or zinc silicate, the surface-specific activity decreases significantly for copper particles smaller than 8?nm, thus revealing structure sensitivity. In view of recent theoretical studies we propose that the methanol synthesis reaction takes place at copper surface sites with a unique configuration of atoms such as step-edge sites, which smaller particles cannot accommodate.

| S-EPMC5476790 | biostudies-literature

Interfacial Defects Dictated In Situ Fabrication of Yolk-Shell Upconversion Nanoparticles by Electron-Beam Irradiation.

Project description:Homogeneous core-shell structured nanoparticles (NPs) are prevailingly designed to accommodate lanthanide emitters, and such an epitaxial shell deposited on core NP is generally believed to help eliminate surface traps or defects on the as-prepared core. However, upon electron-beam irradiation to core-shell-shell NaLuF4:Gd/Yb/Er@NaLuF4:Nd/Yb@NaLuF4 upconversion NPs (UCNPs), it is revealed that interfacial defects actually exist at the core-shell and shell-shell interfaces, even with a higher density than the bulk-phase defects in inner core. Because of such higher density of interfacial defects, the kinetic energies transferred from energetic electrons to atoms may trigger the faster Na/F atom ejections and outward atom migrations in the coating layers than in the inner core of NPs, which ultimately results in the in situ formation of novel yolk-shell UCNPs. These findings provide new insights into interfacial defects in homogeneous core-shell structured NaLnF4 NPs, and pave the way toward utilizing the interactions of high-energy particles with materials for in situ fabrication of novel nanostructures.

| S-EPMC6193145 | biostudies-literature

VOx/Fe2O3 Shell-Core Catalysts for the Selective Oxidation of Methanol to Formaldehyde.

Project description:Efficient oxidation catalysts are important in many current industrial processes, including the selective oxidation of methanol to formaldehyde. Vanadium-containing catalysts have been shown to be effective selective oxidation catalysts for certain reactions, and research continues to examine their applicability to other reactions of interest. Several VOx/Fe2O3 shell-core catalysts with varying VOx coverage have been produced to investigate the stability of VOx monolayers and their selectivity for methanol oxidation. Catalyst formation proceeds via a clear progression of distinct surface species produced during catalyst calcination. At 300 °C the selective VOx overlayer has formed; by 500 °C a sandwich layer of FeVO4 arises between the VOx shell and the Fe2O3 core, inhibiting iron cation participation in the catalysis and enhancing catalyst selectivity. The resulting catalysts, comprising a shell-subshell-core system of VOx/FeVO4/Fe2O3, possess good catalytic activity and selectivity to formaldehyde.

| S-EPMC6560683 | biostudies-literature

Synthesis of dimethyl carbonate from methanol and CO<sub>2</sub> under low pressure.

Project description:A mild and highly efficient approach has been developed for the direct synthesis of dimethyl carbonate (DMC) from methanol and CO2 under low initial pressure. The key to a successful transformation is the use of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), CH2Br2 and ionic liquid. Under the optimized reaction conditions, the yield of DMC was obtained up to 81% under 0.25 MPa. The direct synthesis of DMC can be carried out at balloon pressure using CH2Br2 and DBU. In this case, after the reaction, DBU was proved to be recyclable after having been treated with KOH in ethanol. In addition, a plausible mechanism for this synthetic reaction was proposed according to the experimental results.

| S-EPMC9043122 | biostudies-literature

Synthesis of Dimethyl Carbonate by Transesterification of Propylene Carbonate with Methanol on CeO2-La2O3 Oxides Prepared by the Soft Template Method.

Project description:In this study, CeO2, La2O3, and CeO2-La2O3 mixed oxide catalysts with different Ce/La molar ratios were prepared by the soft template method and characterized by different techniques, including inductively coupled plasma atomic emission spectrometry, X-ray diffraction, N2 physisorption, thermogravimetric analysis, and Raman and Fourier transform infrared spectroscopies. NH3 and CO2 adsorption microcalorimetry was also used for assessing the acid and base surface properties, respectively. The behavior of the oxides as catalysts for the dimethyl carbonate synthesis by the transesterification of propylene carbonate with methanol, at 160 °C under autogenic pressure, was studied in a stainless-steel batch reactor. The activity of the catalysts was found to increase with an increase in the basic sites density. The formation of dimethyl carbonate was favored on medium-strength and weak basic sites, while it underwent decomposition on the strong ones. Several parasitic reactions occurred during the transformation of propylene carbonate, depending on the basic and acidic features of the catalysts. A reaction pathway has been proposed on the basis of the components identified in the reaction mixture.

| S-EPMC8432469 | biostudies-literature

Methanol Dehydration to Dimethyl Ether on Zr-Loaded P-Containing Mesoporous Activated Carbon Catalysts.

Project description:Activated carbons have been prepared by the chemical activation of olive stones with phosphoric acid and loaded with Zr. The addition of Zr to the phosphorus-containing activated carbons resulted in the formation of zirconium phosphate surface groups. Gas phase methanol dehydration has been studied while using the prepared Zr-loaded P-containing activated carbons as catalysts. Carbon catalysts showed high steady-state methanol conversion values, which increased with Zr loading up to a limit that was related to P content. The selectivity towards dimethyl ether was higher than 95% for all Zr loadings. Zirconium phosphate species that were present on catalysts surface were responsible for the catalytic activity.

| S-EPMC6651118 | biostudies-literature

Co-transesterification of waste cooking oil, algal oil and dimethyl carbonate over sustainable nanoparticle catalysts.

Project description:Key challenges for the application of biodiesel include their high acid value, high viscosity, and low ester content. It is essential to develop later-generation biodiesel from unexploited non-food resources for a more sustainable future. Reuse of biowaste is critically important to address these issues of food safety and sustainability. Thus, the co-transesterification of waste cooking oil (WCO), algal oil (AO) and dimethyl carbonate (DMC) for the synthesis of fatty acid methyl esters (FAMEs) was investigated over a series of nanoparticle catalysts containing calcium, magnesium, potassium or nickel under mild reaction conditions. Nanoparticle catalyst samples were prepared from biowaste sources of chicken manure (CM), water hyacinth (WH) and algal bloom (AB), and characterized using XRD, Raman and FESEM techniques for the heterogeneous production of biodiesel. The catalyst was initially prepared by calcination at 850 °C for 4 h in a major presence of CaxMgyCO3, KCl and K2CO3. The WCO and AO co-conversion of 98% and FAMEs co-selectivity of 95% were obtained over CM nanoparticle catalyst under the reaction conditions of 80 °C, 20 mins and DMC to oil molar ratio of 6:1 with 3% catalyst loading and 3% methanol addition. Under the optimum condition, the density, viscosity, and cetane number of the biodiesel were in the range of diesel standards. Nanoparticle catalysts have been proven as a promising sustainable material in the catalytic transesterification of WCO and AO with the major presence of calcium, magnesium and potassium. This study highlights a sustainable approach via biowaste utilization for the enhancement of biodiesel quality with high ester content, low acid value, high cetane number, and low viscosity.

| S-EPMC7494454 | biostudies-literature

The Fabrication and High-Efficiency Electromagnetic Wave Absorption Performance of CoFe/C Core-Shell Structured Nanocomposites.

Project description:CoFe/C core-shell structured nanocomposites (CoFe@C) have been fabricated through the thermal decomposition of acetylene with CoFe2O4 as precursor. The as-prepared CoFe@C was characterized by X-ray powder diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, transmission electron microscopy, and thermogravimetric analysis. The results demonstrate that the carbon shell in CoFe@C has a poor crystallization with a thickness about 5-30 nm and a content approximately 48.5 wt.%. Due to a good combination between intrinsic magnetic properties and high-electrical conductivity, the CoFe@C exhibits not only excellent absorption intensity but also wide frequency bandwidth. The minimum RL value of CoFe@C can reach - 44 dB at a thickness of 4.0 mm, and RL values below - 10 dB is up to 4.3 GHz at a thickness of 2.5 mm. The present CoFe@C may be a potential candidate for microwave absorption application.

| S-EPMC5834946 | 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