Search results for "Chemical engineering"

showing 10 items of 5892 documents

Ni@Fe2O3 heterodimers: controlled synthesis and magnetically recyclable catalytic application for dehalogenation reactions

2012

Ni@Fe2O3 heterodimer nanoparticles (NPs) were synthesized by thermal decomposition of organometallic reactants. After functionalization, these Ni@Fe2O3 heterodimers became water soluble. The pristine heterodimeric NPs were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Mossbauer spectroscopy and magnetic susceptibility measurements. A special advantage of the heterodimers lies in the fact that nanodomains of different composition can be used as catalysts for the removal of environmentally hazardous halogenated pollutants.

inorganic chemicalsChemical engineeringTransmission electron microscopyChemistryMössbauer spectroscopyThermal decompositionHalogenationOrganic chemistryNanoparticleSurface modificationGeneral Materials ScienceMagnetic susceptibilityCatalysisNanoscale
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Removal of Fe(III) from synthetic wastewater into raw and modified clay: Experiments and models fitting

2017

Water pollution by heavy metal ions has become a serious environmental issue especially due to their toxicity and tendency to bioaccumulation. Natural smectite clay was treated using sulfuric acid ...

inorganic chemicalsChemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringMetal ions in aqueous solutionInorganic chemistryFiltration and SeparationSulfuric acid02 engineering and technologyGeneral Chemistry010501 environmental sciencescomplex mixtures01 natural scienceschemistry.chemical_compound020401 chemical engineeringWastewaterBioaccumulationEnvironmental chemistrySorption isotherm0204 chemical engineeringWater pollutionClay minerals0105 earth and related environmental sciencesSeparation Science and Technology
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Incorporation of dynamic boronate links and Ag nanoparticles into PVA hydrogels for pH-Regulated and prolonged release of methotrexate

2021

Abstract In this study, pH-responsive hydrogels based on PVA-boronate crosslinks were prepared via a simple route and used for controlled and targeted delivery of anticancer drug methotrexate. A double network (DN) hydrogel composed of didiol-boronate/PVA complex as the first network and PVA crystallites generated by a freeze-thaw process as the second one was developed. The swelling of PVA-boronate DN hydrogels demonstrated high sensitivity to multiple stimuli including the pH, temperature, and ionic strength of the media thanks to the dynamic boronate links in the first network. Moreover, unlike previously reported hydrogels based on the boronate linkages, the new DN hydrogels preserved t…

inorganic chemicalsChemistrytechnology industry and agricultureCancer therapyPharmaceutical ScienceAg nanoparticlesmacromolecular substances02 engineering and technology021001 nanoscience & nanotechnologycomplex mixtures030226 pharmacology & pharmacyAnticancer drug03 medical and health sciences0302 clinical medicineChemical engineeringProlonged releaseIonic strengthSelf-healing hydrogelsmedicineMethotrexateSwellingmedicine.symptom0210 nano-technologymedicine.drugJournal of Drug Delivery Science and Technology
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Enhanced Heterogeneous Catalytic Conversion of Furfuryl Alcohol into Butyl Levulinate

2014

We study the catalytic condensation of furfuryl alcohol with 1-butanol to butyl levulinate. A screening of several commercial and as-synthesized solid acid catalysts shows that propylsulfonic acid-functionalized mesoporous silica outperforms the state-of-the-art phosphotungstate acid catalysts. The catalyst is prepared via template-assisted sol-gel polycondensation of TEOS and MPTMS. It gives 96 % yield (and 100 % selectivity) of butyl levulinate in 4h at 110 °C. Reaction profiles before and after a hot filtration test confirm that the active catalytic species do not leach into the solution. The catalyst synthesis, characterization, and mode of operation are presented and discussed. Sour ca…

inorganic chemicalsCondensation polymerGeneral Chemical EngineeringesterificationNiobiumHeterogeneous catalysisCatalysisCatalysisFurfuryl alcoholalcoholschemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryGeneral Materials ScienceFuransbiomassorganic chemicalsCondensationMesoporous silicasolid acidsSilicon DioxideLevulinic AcidsGeneral Energyheterogeneous catalysischemistryYield (chemistry)ZeolitesPolystyrenesSulfonic AcidsSelectivityChemSusChem
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Monolayer graphene doping and strain dynamics induced by thermal treatments in controlled atmosphere

2018

Time dynamics of doping and strain induced in single layer graphene by thermal treatments up to 300 degrees C in vacuum, nitrogen, carbon dioxide and oxygen controlled atmosphere are deeply studied by Raman spectroscopy and they are compared with its morphological evolution investigated by Atomic Force Microscopy. The reaction dynamics in oxygen treatments is determined down to a time scale of few minutes as well as that of dedoping process made by water vapor treatment. The interplay of strain modification and doping effects is separated. The strain is clarified to be strongly influenced by the cooling time. The doping removal is dominated by the water vapor, showing that the concentration…

inorganic chemicalsControlled atmosphereAnalytical chemistrychemistry.chemical_element02 engineering and technologydoping010402 general chemistry01 natural sciencesOxygenStrainAtmosphereCondensed Matter::Materials Sciencesymbols.namesakeThermalGeneral Materials ScienceRamanDopinggraphenetechnology industry and agricultureGeneral Chemistry021001 nanoscience & nanotechnologyNitrogen0104 chemical scienceschemistryChemical engineeringGraphene Thermal Doping Chemistry (all)symbolsAFM0210 nano-technologyRaman spectroscopyWater vapor
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The reduction of molecular oxygen by iron porphyrins

2002

Abstract Molecular assemblies have been synthesised to reproduce the structure of the cytochrome c oxidase (C c O) active site and to explore the roles played by its different features. It was discovered that a single iron porphyrin, adsorbed at the surface of a graphite electrode, is a selective catalyst for the four-electron reduction of dioxygen to water, at pH 7. To cite this article: D. Ricard et al., C. R. Chimie 5 (2002) 33–36

inorganic chemicalsCytochromebiology010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryActive sitechemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistryElectrocatalyst01 natural sciencesPorphyrinOxygen[ CHIM ] Chemical Sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistry[CHIM] Chemical Sciencesbiology.proteinCytochrome c oxidase[CHIM]Chemical SciencesGraphite
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Oxidative dehydrogenation of ethane: A study over the structure and robustness of Ni–W–O catalysts

2014

[EN] The robustness of one selected Ni-W-O catalyst has been studied in the oxidative dehydrogenation of ethane. This catalyst initially deactivates for the first 10 h online decreasing 15% of its catalytic activity compared to its initial stable catalytic activity. However from 10 to 60 h online the catalytic activity keeps almost stable. On the other hand, it has been shown that the Ni-W-O catalyst cannot tolerate an oxygen-free atmosphere (C-2 and He) as nickel oxide is transformed into metallic nickel. Methane and hydrogen as well as abundant coke were formed on the surface of the catalyst in these O-free conditions. However a re-calcination in air leads to the removal of coke, the cata…

inorganic chemicalsEthyleneHydrogenGeneral Chemical EngineeringCatalyst supportInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementCatalysisMethaneCatalysisEthylenechemistry.chemical_compoundDehydrogenationNickel tungstenOxidative dehydrogenation of ethaneOxide catalystsEthaneChemistryorganic chemicalsNickel oxideCokeFuel TechnologyNi-W-OHydrogenOxidative dehydrogenationFuel Processing Technology
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A Study on Acidification and Intercalation of Illite Clay Minerals and their Potential Use as a Filler in SPEEK Composite Membranes

2018

The acidification and intercalation of illite containing clays were studied for potential use as fillers for sulphonated poly (ether ether ketone) (SPEEK) composite membrane preparation and future proton exchange membrane fuel cells application. The acidification and dimethyl sulfoxide (DMSO) intercalation of illite clays have been studied by powder X-ray diffractometry, X-ray fluorescence spectrometry, and thermogravimetric analysis. SPEEK composite membranes were made with 1, 3 and 5% purified, acidified, DMSO intercalated clay fillers. SPEEK/clay composite membranes were characterized by proton conductivity, water uptake, and mechanical strength.

inorganic chemicalsFiller (packaging)Materials science020209 energyMechanical EngineeringIntercalation (chemistry)Composite number02 engineering and technologyengineering.material021001 nanoscience & nanotechnologycomplex mixturesMembraneChemical engineeringMechanics of MaterialsIllite0202 electrical engineering electronic engineering information engineeringengineeringGeneral Materials ScienceComposite membrane0210 nano-technologyClay mineralsKey Engineering Materials
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AlTf-UVM-7—Highly active catalysts for the synthesis of long chain symmetrical ethers and non-ionic surfactant structures

2010

New Lewis acid AlTf-UVM-7 catalysts with bimodal pore system and different Si to Al ratios were prepared in a two-step synthesis in which triflic acid (Tf) was incorporated into previously synthesized mesoporous aluminum-containing silica. The Al incorporation inside the pore walls was carried out through the Atrane method. The characterization of the resulted catalysts showed that the triflic acid treatment step did not damage the texture or the structure of the catalysts. These materials were used as green catalysts for the etherification of fatty alcohols and the conversion of ethylene glycol (EG) with n-octanol resulting in mixtures of short ethoxylated structures with a large distribut…

inorganic chemicalsGeneral Chemical EngineeringGeneral ChemistryIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundchemistryPulmonary surfactantAtraneEnvironmental ChemistryOrganic chemistryLewis acids and basesMesoporous materialTriflic acidChemical compositionEthylene glycolChemical Engineering Journal
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Porous clays heterostructures as supports of iron oxide for environmental catalysis

2018

[EN] Porous Clays Heterostructures (PCH) from natural pillared clays (bentonite with a high proportion of montmorillonite) have been used as supports of iron oxide for two reactions of environmental interest: i) the elimination of toluene (a representative compound of one of the most toxic subsets of volatile organic compounds, aromatics) by total oxidation and ii) the selective oxidation of H2S to elemental sulfur. For both reactions these catalysts have resulted to be remarkably more efficient than similar catalysts prepared using conventional silica as a support. Thus, in the total oxidation of toluene it has been observed that the catalytic activity obtained using siliceous PCH is two o…

inorganic chemicalsGeneral Chemical EngineeringInorganic chemistryIron oxidechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundH2S to STotal and selective oxidationIron oxideEnvironmental ChemistrySulfatePorous Clays Heterostructures (PCH)ChemistryVOCGeneral Chemistry021001 nanoscience & nanotechnologySulfurToluene0104 chemical sciencesMontmorilloniteBentonite0210 nano-technologySelectivityTolueneChemical Engineering Journal
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