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Conversion of methanol over 10-ring zeolites with differing volumes at channel intersections: comparison of TNU-9, IM-5, ZSM-11 and ZSM-5.Conversion of methanol to hydrocarbons: how zeolite cavity and pore size controls product selectivity.The formation and degradation of active species during methanol conversion over protonated zeotype catalysts.Optical investigation of the intergrowth structure and accessibility of Brønsted acid sites in etched SSZ-13 zeolite crystals by confocal fluorescence microscopy.Thermochemistry of organic reactions in microporous oxides by atomistic simulations: benchmarking against periodic B3LYP.Probing the surface of nanosheet H-ZSM-5 with FTIR spectroscopy.Quantum chemical modeling of zeolite-catalyzed methylation reactions: toward chemical accuracy for barriers.Theoretical study of ethylbenzenium ions: the mechanism for splitting off ethene, and the formation of a pi complex of ethene and the benzenium ion.Does an ethene/benzenium ion complex exist? A discrepancy between B3LYP and MP2 predictions.Conversion of methanol to hydrocarbons over zeolite ZSM-23 (MTT): exceptional effects of particle size on catalyst lifetime.Time- and space-resolved study of the methanol to hydrocarbons (MTH) reaction - influence of zeolite topology on axial deactivation patterns.A Systematic Study of Isomorphically Substituted H-MAlPO-5 Materials for the Methanol-to-Hydrocarbons Reaction.Methane to Methanol: Structure-Activity Relationships for Cu-CHA.Topology-dependent hydrocarbon transformations in the methanol-to-hydrocarbons reaction studied by operando UV-Raman spectroscopyA XAFS study of the local environment and reactivity of Pt- sites in functionalized UiO-67 MOFsSingle-Event MicroKinetics (SEMK) for Methanol to Hydrocarbons (MTH) on H-ZSM-23Single-Event Microkinetics for Methanol to Olefins on H-ZSM-5The nuclearity of the active site for methane to methanol conversion in Cu-mordenite: a quantitative assessmentEffect of Benzoic Acid as a Modulator in the Structure of UiO-66: An Experimental and Computational StudyProbing Reactive Platinum Sites in UiO-67 Zirconium Metal–Organic FrameworksStructure–deactivation relationships in zeolites during the methanol–to-hydrocarbons reaction: Complementary assessments of the coke contentZeolite morphology and catalyst performance: conversion of methanol to hydrocarbons over offretiteDefect Engineering: Tuning the Porosity and Composition of the Metal–Organic Framework UiO-66 via Modulated SynthesisDetailed Structure Analysis of Atomic Positions and Defects in Zirconium Metal–Organic FrameworksMethanol Conversion to Hydrocarbons (MTH) Over H-ITQ-13 (ITH) ZeoliteTuned to Perfection: Ironing Out the Defects in Metal–Organic Framework UiO-66Catalyst deactivation by coke formation in microporous and desilicated zeolite H-ZSM-5 during the conversion of methanol to hydrocarbonsIn Situ Infrared Spectroscopic and Gravimetric Characterisation of the Solvent Removal and Dehydroxylation of the Metal Organic Frameworks UiO-66 and UiO-67Unit cell thick nanosheets of zeolite H-ZSM-5: Structure and activityAssessing the surface sites of the large pore 3-dimensional microporous material H-ITQ-7 using FT-IR spectroscopy and molecular probesHow defects and crystal morphology control the effects of desilicationInfrared Spectroscopic Investigation of the Acidity and Availability of the Surface Hydroxyls of Three-Dimensional 12-Ring Zeotype H-ITQ-7Methane conversion to light olefins—How does the methyl halide route differ from the methanol to olefins (MTO) route?Synthesis of Titanium Chabazite: A New Shape Selective Oxidation Catalyst with Small Pore Openings and Application in the Production of Methyl Formate from MethanolAssessing the acid properties of desilicated ZSM-5 by FTIR using CO and 2,4,6-trimethylpyridine (collidine) as molecular probesThe Effect of Acid Strength on the Conversion of Methanol to Olefins Over Acidic Microporous Catalysts with the CHA TopologyConversion of methanol to hydrocarbons over zeolite H-ZSM-5: On the origin of the olefinic speciesUnderstanding and Optimizing the Performance of Cu‐FER for The Direct CH 4 to CH 3 OH ConversionFunctionalizing the Defects: Postsynthetic Ligand Exchange in the Metal Organic Framework UiO-66High Zn/Al ratios enhance dehydrogenation vs hydrogen transfer reactions of Zn-ZSM-5 catalytic systems in methanol conversion to aromatics
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Q33448937-087485C5-7479-4C17-A127-FD7CB9B0ADA3Q38003355-79DC0CC0-2F91-44E8-B652-B6EC91C06565Q38549268-80914C12-C692-4FD5-B919-FFF48E203CACQ43055739-EC0DD030-1ECE-4972-BCE1-231973B6C715Q43643723-74D10724-DB43-4B8D-976B-40D7D315FE4EQ45907703-68F36D86-A406-4E2D-888E-C062D00D0BE3Q46188581-190F2C51-164A-4DE3-B6CA-008F79C06B0FQ46188615-8C36F0C9-5D44-44DD-82B0-790CD67A3F8AQ46508168-EE3C0E0F-A1CC-4974-B075-D3F664BF95DEQ47210053-CAB74BA3-FEAC-4EDC-88B0-F0A65288F5B3Q47828432-6DAED390-F8C5-4D4F-B48D-FA6E186B9206Q48102379-41E57BCD-1324-4A93-B6DA-28EA537A24C2Q48295471-970C23C0-6AE6-4664-A027-AD08C4EFE00EQ57281517-A1693BE1-3224-4567-9CB5-74DD258E838FQ57596983-73E3D675-08C0-4657-9D13-2984F905DFCFQ57723809-AA6C8C4A-3D99-448F-8939-8801B2143CC1Q57723816-59F0E7FF-1251-42C0-83F8-63C16ED33191Q57803392-8BB13F9E-8457-4548-A03C-09989284982AQ57886982-6505D9FA-115C-4D64-B6D0-C71234C31A7BQ60165892-80031D50-AD29-4E0A-999B-315AB76D1589Q60168937-11DE45D4-33BB-47CF-B9C6-D0AAB1563709Q60168942-31C18CCE-A944-47E1-AA4E-82101C722D6EQ60168945-6DF29FF0-6804-47BD-B16B-26FBBE05535CQ60168978-8023F547-D7C0-43B9-B720-6CB4A9B20CC2Q60168979-1DF535DD-4878-4CD7-B35D-25F7E993592FQ60168983-EBF4331D-FAE0-48B7-A79A-8E1A0998B36CQ60168986-6640A42E-BC22-40BF-B71C-728DFB8A99E1Q60168998-05A7732C-789E-43B3-A4F5-58B7B67F7F5FQ60169007-431D3662-4671-4657-9906-27E3F97862EAQ60169032-6F835DF7-C22D-4718-8825-51870AC79936Q60169041-D3DD2D85-A506-4EEA-9109-956D2F88DAA6Q60169042-FE1EE932-2FBC-46A2-928D-31DF983266FBQ60169044-EA7EE9E2-3B32-496D-B75E-40028B78AF0DQ60169050-214DFC19-EC79-43DE-B3EA-DCABEAD78250Q60169068-BF59D38D-2869-49E4-8A08-6C216AFAB954Q60169081-8E4861A9-01CD-4E58-A686-38D25860AB04Q60169106-CCC6C27B-8328-414D-BEB8-FD6A0C78333FQ60320951-CF8D2B93-2655-4E63-9006-659DDBF8B3A9Q60429979-D2B5CBCC-339D-4FDD-B553-B153562BDD40Q60448481-64B0F9B0-50E4-477B-9676-4FE8D30A7EBA
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description
Noors professor
@nl
Norwegian chemist and professor at University of Oslo
@en
norsk kjemiker og professor ved Universitetet i Oslo
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norsk kjemiker og professor ved Universitetet i Oslo
@nn
name
Stian Svelle
@ast
Stian Svelle
@ca
Stian Svelle
@da
Stian Svelle
@de
Stian Svelle
@en
Stian Svelle
@es
Stian Svelle
@fr
Stian Svelle
@ga
Stian Svelle
@nb
Stian Svelle
@nl
type
label
Stian Svelle
@ast
Stian Svelle
@ca
Stian Svelle
@da
Stian Svelle
@de
Stian Svelle
@en
Stian Svelle
@es
Stian Svelle
@fr
Stian Svelle
@ga
Stian Svelle
@nb
Stian Svelle
@nl
prefLabel
Stian Svelle
@ast
Stian Svelle
@ca
Stian Svelle
@da
Stian Svelle
@de
Stian Svelle
@en
Stian Svelle
@es
Stian Svelle
@fr
Stian Svelle
@ga
Stian Svelle
@nb
Stian Svelle
@nl
P106
P1015
P1015
P21
P214
375149066544265601303
P2287
P27
P31
P496
0000-0002-7468-5546
P569
1975-01-01T00:00:00Z
P734
P735
P7859
viaf-375149066544265601303