0000000001307520

AUTHOR

Nicole Beiser

showing 11 related works from this author

Sustainable access to biobased biphenol epoxy resins by electrochemical dehydrogenative dimerization of eugenol

2019

Limited fossil resources require innovative monomers and polymers derived from renewable feedstocks such as plant biomass. Thermosetting epoxy resins largely rely on petrochemical bisphenol-type monomers, which give high performance materials but are controversial due to their effects on human health. Herein, we present two biobased epoxy resins by direct dehydrogenative dimerization of eugenol, the main component of clove oil. Taking the Principles of Green Chemistry into account, we developed electrochemical dehydrodimerization at reticulated vitreous carbon (RVC) electrodes using methanol as environmentally benign solvent. Thus, fluorinated solvents such as 1,1,1,3,3,3-hexafluoroisopropa…

Green chemistrychemistry.chemical_classification010405 organic chemistryThermosetting polymerPolymerEpoxy010402 general chemistry01 natural sciencesPollution0104 chemical sciencesSolventchemistry.chemical_compoundPetrochemicalchemistryvisual_artvisual_art.visual_art_mediumEnvironmental ChemistryOrganic chemistryMethanolCuring (chemistry)Green Chemistry
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Biobased Epoxy Resin by Electrochemical Modification of Tall Oil Fatty Acids

2019

A biobased epoxy resin was prepared from tall oil fatty acids (TOFAs), a byproduct of the pulping industry. As free carboxylic acids compromise resin stability, TOFA was subjected to non-Kolbe decarboxylation to give alkenes upon loss of CO2. Thereby, the degree of unsaturation is significantly increased. This electrosynthetic protocol using an undivided cell setup and inexpensive graphite electrodes in a galvanostatic operation mode was scaled to a 1.5 L reactor, making use of electric current as a green and waste-free reagent. Simple, cost-efficient epoxidation using oxone subsequently gives an epoxy resin of low viscosity. Curing with anhydrides yields thermoset materials. Dynamic mechan…

Degree of unsaturationMaterials scienceRenewable Energy Sustainability and the EnvironmentTall oilDecarboxylationGeneral Chemical EngineeringThermosetting polymer02 engineering and technologyGeneral ChemistryEpoxy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesChemical engineeringFlexural strengthReagentvisual_artvisual_art.visual_art_mediumEnvironmental Chemistry0210 nano-technologyCuring (chemistry)ACS Sustainable Chemistry & Engineering
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Adsorption and separation of black liquor-derived phenol derivatives using anion exchange resins

2017

Abstract Kraft black liquor is the major waste stream of the paper pulping industry. This stream is usually directly incinerated in such facilities for energy production and recycling of the inorganic chemicals involved. However, lignin and other low molecular organic fragments dissolved in black liquor give rise to a large variety of aromatic fine chemicals. Energetic use of black liquor and its components prevents the removal of these valuable compounds from the waste stream. We present an easy protocol for adsorption and selective desorption of low molecular phenol derivatives from black liquor depending on the composition of the desorption system. Furthermore, adsorption experiments in …

Ion exchange010405 organic chemistryChemistryfood and beveragesFiltration and Separation010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryIncinerationchemistry.chemical_compoundAdsorptionDesorptionOrganic chemistryPhenolIon-exchange resinBlack liquorKraft paperSeparation and Purification Technology
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Investigations on isomerization and rearrangement of polycyclic arenes under oxidative conditions – Anodic versus reagent-mediated reactions

2019

Abstract Electro-organic conversions at an active molybdenum anode enable the formation of fused arenes. High chemoselectivity was achieved under anodic conditions, and a reagent-induced selectivity was observed by comparison with results of MoCl5-mediated reactions. Polycyclic arenes like phenanthrenes, triphenylenes, chrysenes, or helicenes were selectively obtained in yields up to 87% and in some cases unusual rearrangements were crucial for the product formation.

General Chemical Engineeringchemistry.chemical_elementOxidative couplingRearrangement02 engineering and technologyOxidative phosphorylation010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesElectrolysis0104 chemical sciencesAnodeAnodechemistryMolybdenumReagentElectrochemistryPhenanthrenesChemoselectivityPolycyclic arenes0210 nano-technologySelectivityIsomerizationElectrochimica Acta
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Anodic Degradation of Lignin at Active Transition Metal-based Alloys and Performance-enhanced Anodes

2018

010405 organic chemistryChemistryVanillin010402 general chemistryElectrochemistry01 natural sciencesCatalysis0104 chemical sciencesAnodechemistry.chemical_compoundTransition metalChemical engineeringElectrochemistryDegradation (geology)LigninChemElectroChem
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CCDC 1882077: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters2367-tetramethoxy-1-phenyltriphenyleneExperimental 3D Coordinates
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CCDC 1882075: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters3-(34-dimethoxyphenyl)-171011-tetramethoxytriphenylene dichloromethane solvateExperimental 3D Coordinates
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CCDC 1882076: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

914-bis(ethoxycarbonyl)-2367-tetramethoxy[5]heliceneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1882073: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

diethyl 2351011-pentamethoxybenzo[c]chrysene-814-dicarboxylateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1882074: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersdiethyl 6789-tetramethoxybenzo[ghi]perylene-411-dicarboxylate dichloromethane solvateExperimental 3D Coordinates
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CCDC 1882078: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

23561011-hexamethoxy-8-methylbenzo[e]acephenanthryleneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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