0000000000267746

AUTHOR

Dirk De Vos

showing 19 related works from this author

Direct Synthesis of Aluminosilicate IWR Zeolite from a Strong Interaction between Zeolite Framework and Organic Template.

2019

A large amount of zeolite structures are still not synthetically available or not available in the form of aluminosilicate currently. Despite significant progress in the development of predictive concepts for zeolite synthesis, accessing some of these new materials is still challenging. One example is the IWR structure as well. Despite successful synthesis of Ge-based IWR zeolites, direct synthesis of aluminosilicate IWR zeolite is still not successful. In this report we show how a suitable organic structure directing agent (OSDA), through modeling of an OSDA/zeolite cage interaction, could access directly the aluminum-containing IWR structure (denoted as COE-6), which might allow access to…

General Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundColloid and Surface ChemistrychemistryChemical engineeringAluminosilicateGeneral chemistryHydrothermal synthesisMethanolZSM-5SelectivityZeoliteJournal of the American Chemical Society
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Recent advances in the preparation of zeolites for the selective catalytic reduction of NOx in diesel engines

2019

Metal-exchanged zeolites with small pore sizes have attracted much attention in recent years due to their application in the selective catalytic reduction (SCR) of NOx in diesel engines. Typically, copper-chabazite (e.g. Cu-SSZ-13) has been gradually used as an SCR catalyst in heavy-duty diesel vehicles over the last decade due to its relatively excellent catalytic performance and stability. However, most SSZ-13 zeolites are still prepared via the traditional hydrothermal process in the presence of organic templates, requiring consecutive solid separation and thermal treatment steps to achieve the final zeolite products. In recent years, several strategies for the environmentally friendly p…

Fluid Flow and Transfer ProcessesDiesel fuelMaterials scienceChemical engineeringChemistry (miscellaneous)Process Chemistry and TechnologyChemical Engineering (miscellaneous)Selective catalytic reductionZeoliteEnvironmentally friendlyCatalysisNOxCatalysisReaction Chemistry & Engineering
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Fe-doped Beta zeolite from organotemplate-free synthesis for NH3-SCR of NOx

2016

Two types of Beta zeolites, one from organotemplate-free synthesis with a Si/Al ratio of 9 and the other from a commercial one with a Si/Al ratio of 19, were employed here to dope Fe for NH3-SCR of NOx. Fe-Beta (Si/Al = 9) exhibits much higher activity than Fe-Beta (Si/Al = 19), especially at low-temperature regions (<250 °C). In addition, it also exhibits better hydrothermal stability as compared with Fe-Beta (Si/Al = 19), which demonstrates that it is a promising SCR catalyst with good activity as well as hydrothermal stability. The correlation between the quantitative calculation of the content of isolated Fe3+ in Beta zeolites and the NO conversion rate at 150 °C shows a linear relation…

inorganic chemicalsChemistryInorganic chemistryNo conversion02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysisHydrothermal circulation0104 chemical sciencesCatalysisLinear relationshipFe doped0210 nano-technologyZeoliteBeta (finance)NOx
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Improvement of catalytic activity over Cu--Fe modified Al-rich Beta catalyst for the selective catalytic reduction of NOx with NH3

2016

Copper and iron bimetal modified Al-rich Beta zeolites from template-free synthesis were prepared for selective catalytic reduction (SCR) of NOx with NH3 in exhaust gas streams. Comparing to the Cu-based and Fe-based mono-component Beta catalysts, Cu(3.0)-Fe(1.3)-Beta bi-component catalyst shows better low-temperature activity and wider reaction-temperature window. Over 80% of NO conversion can be achieved at the temperature region of 125–500 °C. Due to the synergistic effect of copper and iron evidenced by XRD, UV–Vis–NIR, EPR and XPS measurements, the dispersion state of active components as well as the ratio of Cu2+/Cu+ and Fe3+/Fe2+ were improved over Cu(3.0)-Fe(1.3)-Beta. Isolated Cu2+…

inorganic chemicalsInorganic chemistryCu--Fe-Betachemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistryDispersion (geology)01 natural sciencesCatalysisBimetalAl-rich BetaX-ray photoelectron spectroscopyGeneral Materials ScienceNOxSelective catalytic reductionGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsCopperSulfur0104 chemical scienceschemistryMechanics of MaterialsSynergistic effect0210 nano-technologyNH3-SCR
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Expanding the Variety of Zirconium‐based Inorganic Building Units for Metal–Organic Frameworks

2019

Two new zirconium-based metal-organic frameworks with the composition [Zr6 O4 (OH)4 (OAc)6 (BDC)3 ] (CAU-26) and [Zr5 O4 (OH)4 (OAc)4 (BDC)2 ] (CAU-27) are reported, which were synthesized from acetic acid, a rarely utilized but green and sustainable solvent (BDC2- : 1,4-benzenedicarboxylate). Structure determination aided by automated electron diffraction tomography revealed that CAU-26 is composed of layers of well-known {Zr6 O8 } clusters interconnected by terephthalate ions. In contrast CAU-27 exhibits a three-dimensional structure with a so far unknown type of one-dimensional inorganic building unit (IBU), which can be rationalized as condensed polyhedron-sharing chains of {Zr6 O8 } cl…

Green chemistryMaterials scienceChemistry MultidisciplinaryCATALYZED BORYLATIONchemistry.chemical_element010402 general chemistryHIGHLY EFFICIENTBorylation01 natural sciencesTOXICITYCatalysisCatalysisAUTOMATED DIFFRACTION TOMOGRAPHYPolymer chemistryMoleculeZR-MOFGreen ChemistryZirconiumScience & TechnologySTABILITY010405 organic chemistryDirect C-H borylationGeneral ChemistryGeneral MedicineElectron DiffractionORGANOSILICA0104 chemical sciencesSolventChemistrychemistryPhysical SciencesARENESMetal-organic frameworkChemical stabilityZirconiumCLUSTERSMetal-organic FrameworksGREEN SYNTHESISAngewandte Chemie
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The effect of trivalent framework heteroatoms in Cu-CHA on the Selective Catalytic Reduction of NO

2021

Abstract The effect of the trivalent framework atoms (Si4+/M3+ = 13-105) in Cu exchanged CHA-type zeolites was investigated for the selective catalytic reduction of NO with NH3. While the increased hydrophobicity of B-CHA compared to Al-CHA could make it a good candidate for low temperature SCR, the material was too unstable under reaction conditions and the exchanged Cu2+ did not remain isolated. Consequently a lower activity and selectivity than for Al-CHA were observed. Ga-CHA on the other hand showed a similar Cu2+ speciation as Al-CHA at similar Si4+/M3+ ratios. The difference in catalytic activity was remarkably small. While Ga-CHA was less stable upon hydrothermal aging, this was mar…

Reaction conditionsChemistryProcess Chemistry and Technologymedia_common.quotation_subjectHeteroatomInorganic chemistrySelective catalytic reductionCatalysisHydrothermal circulationCatalysisSpeciationSelectivityZeolitemedia_commonApplied Catalysis A: General
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Rare-earth ion exchanged Cu-SSZ-13 zeolite from organotemplate-free synthesis with enhanced hydrothermal stability in NH3-SCR of NOx

2019

The relatively low hydrothermal stability of Al-rich Cu-SSZ-13 catalysts hinders their practical application in ammonia selective catalytic reduction (NH3-SCR) reaction. Rare-earth ions were introduced into the Al-rich SSZ-13 zeolite using an organotemplate-free synthesis prior to the exchange of Cu2+ ions. Among the rare-earth ions tested (Ce, La, Sm, Y, Yb), Y shows significant enhancement of the hydrothermal stability and NH3-SCR activities after severe hydrothermal aging at 800 °C for 16 h when compared with Cu-SSZ-13 without Y. Cu–Y-SSZ-13 catalysts with various amounts of Y were prepared, and it is found that with increasing Y content, the low temperature NO conversions can be improve…

Materials science010405 organic chemistryInorganic chemistryInfrared spectroscopySelective catalytic reduction010402 general chemistry01 natural sciencesCatalysisHydrothermal circulation0104 chemical sciencesCatalysisSSZ-13AdsorptionTemperature-programmed reductionZeoliteCatalysis Science &amp; Technology
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Automated Diffraction Tomography for the Structure Elucidation of Twinned, Sub-micrometer Crystals of a Highly Porous, Catalytically Active Bismuth M…

2012

010405 organic chemistryChemistrystructure elucidationInorganic chemistrychemistry.chemical_elementGeneral Medicine02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesCatalysis0104 chemical sciencesBismuthbismuth; heterogeneous catalysis; metal-organic frameworks; structure elucidationSub micrometerDiffraction tomographyheterogeneous catalysisChemical engineeringbismuthHighly porousMetal-organic framework0210 nano-technologymetal-organic frameworksAngewandte Chemie International Edition
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Cu-exchanged Al-rich SSZ-13 zeolite from organotemplate-free synthesis as NH3-SCR catalyst: Effects of Na+ ions on the activity and hydrothermal stab…

2017

Abstract The relatively low activity at lower temperatures and high cost of SSZ-13 zeolite from organotemplate synthesis are two of major problems of presently commercialized Cu-SSZ-13 catalysts for NH3-SCR reaction. Cu-exchanged Al-rich SSZ-13 catalysts with Si/Al = 4 from organotemplate-free synthesis have been prepared, and show superior NH3-SCR performance with NO conversions above 85% at wide-temperature window ranging from 150 to 650 °C. Cu-Na-SSZ-13 catalysts with varied amount of residual Na+ were prepared by partial ion-exchange of as-prepared Al-rich Na-SSZ-13, and it’s found that Cu-Na-SSZ-13 catalyst with moderate Na+ content can improve both the low-temperature activity and its…

ChemistryProcess Chemistry and TechnologyInorganic chemistryLow activityHydrothermal treatment02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysisHydrothermal circulation0104 chemical sciencesCatalysisSSZ-130210 nano-technologyZeoliteGeneral Environmental ScienceApplied Catalysis B: Environmental
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Highly stable and porous porphyrin-based zirconium and hafnium phosphonates – electron crystallography as an important tool for structure elucidation

2018

The Ni-metallated porphyrin-based tetraphosphonic acid (Ni-tetra(4-phosphonophenyl)porphyrin, Ni-H8TPPP) was used for the synthesis of highly porous metal phosphonates containing the tetravalent cations Zr4+ and Hf4+. The compounds were thoroughly characterized regarding their sorption properties towards N2 and H2O as well as thermal and chemical stability. During the synthesis optimization the reaction time could be substantially decreased under stirring from 24 to 3 h in glass vials. M-CAU-30, [M2(Ni-H2TPPP)(OH/F)2]·H2O (M = Zr, Hf) shows exceptionally high specific surface areas for metal phosphonates of aBET = 1070 and 1030 m2 g-1 for Zr- and Hf-CAU-30, respectively, which are very clos…

PORESMaterials scienceChemistry Multidisciplinarychemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesAQUEOUS-SOLUTIONMETAL-ORGANIC FRAMEWORKSchemistry.chemical_compoundDESIGNAUTOMATED DIFFRACTION TOMOGRAPHYFormula unitMoleculeCRYSTAL-STRUCTUREZirconiumScience & TechnologySTABILITYGeneral Chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencesChemistryMANGANESE PORPHYRINSCrystallographychemistryElectron diffractionPhysical SciencesLIGANDSChemical stabilityCyclic voltammetry0210 nano-technologySYSTEMChemical Science
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Transformation synthesis of aluminosilicate SSZ-39 zeolite from ZSM-5 and beta zeolite

2019

Aluminosilicate SSZ-39 zeolite has been successfully prepared by transformation from ZSM-5 and beta zeolite in the presence of N,N-diethyl-cis-2,6-dimethylpiperidinium hydroxide (DMPOH) under hydrothermal conditions. Catalytic tests in the selective catalytic reduction of NOx with NH3 (NH3-SCR) show that the copper-exchanged products synthesized from the interzeolite transformation exhibit excellent catalytic performance.

Renewable Energy Sustainability and the EnvironmentChemistrySelective catalytic reduction02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnologyHydrothermal circulationCatalysischemistry.chemical_compoundChemical engineeringAluminosilicateHydroxideGeneral Materials ScienceZSM-50210 nano-technologyZeoliteNOxJournal of Materials Chemistry A
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A Cationic Oligomer as an Organic Template for Direct Synthesis of Aluminosilicate ITH Zeolite

2020

There are a large number of zeolites, such as ITH, that cannot be prepared in the aluminosilicate form. Now, the successful synthesis of aluminosilicate ITH zeolite using a simple cationic oligomer as an organic template is presented. Key to the success is that the cationic oligomer has a strong complexation ability with aluminum species combined with a structural directing ability for the ITH structure similar to that of the conventional organic template. The aluminosilicate ITH zeolite has very high crystallinity, nanosheet-like crystal morphology, large surface area, fully four-coordinated Al species, and abundant acidic sites. Methanol-to-propylene (MTP) tests reveal that the Al-ITH zeo…

010405 organic chemistryChemistryCationic polymerizationchemistry.chemical_elementGeneral MedicineGeneral Chemistry010402 general chemistryCrystal morphology01 natural sciencesOligomerCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallinityChemical engineeringAluminosilicateAluminiumZeoliteSelectivityAngewandte Chemie International Edition
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Efficient and rapid transformation of high silica CHA zeolite from FAU zeolite in the absence of water

2017

High silica CHA zeolite plays an important role in selective catalytic reduction of NOx with NH3 (NH3-SCR), but its synthesis is not highly efficient due to the use of a relatively high-cost structural directing agent (SDA) N,N,N-trimethyl-adamantammonium hydroxide (TMAdaOH) and relatively long crystallization time under hydrothermal conditions. Herein, we report an efficient and rapid synthesis of a high silica CHA zeolite possessing good crystallinity and uniform crystals (CHA-ST). The method includes interzeolite transformation of high silica FAU zeolite in the absence of water but the presence of zeolite seeds and a bromide form of the SDA. The absence of water in the synthesis signific…

ChabaziteMaterials scienceRenewable Energy Sustainability and the EnvironmentInorganic chemistrySelective catalytic reduction02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysislaw.inventionSSZ-13chemistry.chemical_compoundchemistryChemical engineeringBromidelawHydroxideGeneral Materials ScienceCrystallization0210 nano-technologyZeoliteJournal of Materials Chemistry A
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Cu-Exchanged CHA-Type Zeolite from Organic Template-Free Synthesis: An Effective Catalyst for NH3-SCR

2020

A Cu-containing CHA-type zeolite was prepared via aqueous ion exchange of the CHA zeolite from organic template-free synthesis. The thus-obtained template-free Cu-CHA showed the best catalytic perf...

Template freeAqueous solutionIon exchangeChemistryGeneral Chemical Engineering02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnologyMolecular sieveIndustrial and Manufacturing EngineeringCatalysisAmmoniachemistry.chemical_compound020401 chemical engineering0204 chemical engineering0210 nano-technologyZeoliteNOxNuclear chemistryIndustrial &amp; Engineering Chemistry Research
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Highly stable and porous porphyrin-based zirconium and hafnium phosphonates – electron crystallography as an important tool for structure elucidation…

2018

A highly porous and stable Zr-MOF containing a planar porphyrin-based tetraphosphonic acid was synthesized and characterized regarding its sorption properties and chemical stability.

ChemistryChemical Science
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CCDC 1880628: Experimental Crystal Structure Determination

2019

Related Article: Sebastian Leubner, Haishuang Zhao, Niels Van Velthoven, Mickael Henrion, Helge Reinsch, Dirk De Vos, Ute Kolb, Norbert Stock|2019|Angew.Chem.,Int.Ed.|58|10995|doi:10.1002/anie.201905456

Space GroupCrystallographyCrystal Systemcatena-[bis(mu-benzene-14-dicarboxylato)-tetrakis(mu-oxido)-tetrakis(mu-hydroxo)-tetrakis(mu-acetato)-penta-zirconium(iv) hydrate]Crystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 930933: Experimental Crystal Structure Determination

2016

Related Article: Mark Feyand, Enrico Mugnaioli, Frederik Vermoortele, Bart Bueken, Johannes M. Dieterich, Tim Reimer, Ute Kolb, Dirk de Vos, Norbert Stock|2012|Angew.Chem.,Int.Ed.|51|10373|doi:10.1002/anie.201204963

catena-[(mu-44'4''-benzene-135-triyltribenzoato)-bismuth]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1880629: Experimental Crystal Structure Determination

2019

Related Article: Sebastian Leubner, Haishuang Zhao, Niels Van Velthoven, Mickael Henrion, Helge Reinsch, Dirk De Vos, Ute Kolb, Norbert Stock|2019|Angew.Chem.,Int.Ed.|58|10995|doi:10.1002/anie.201905456

Space GroupCrystallographyCrystal Systemcatena-[bis(mu-[11'-biphenyl]-44'-dicarboxylato)-tetrakis(mu-hydroxo)-tetrakis(mu-oxido)-tetrakis(mu-acetato)-penta-zirconium(iv) hydrate]Crystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1831844: Experimental Crystal Structure Determination

2018

Related Article: Timo Rhauderwiek, Haishuang Zhao, Patrick Hirschle, Markus Döblinger, Bart Bueken, Helge Reinsch, Dirk De Vos, Stefan Wuttke, Ute Kolb, Norbert Stock|2018|Chemical Science|9|5467|doi:10.1039/C8SC01533C

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatescatena-[(mu-[{1020-bis[4-(hydroxyphosphinato)phenyl]porphyrinato-515-diyl}di(41-phenylene)]bis(phosphonato))-bis(mu-hydroxo)-nickel-di-zirconium octahydrate]
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