Search results for "Green chemistry"

showing 10 items of 159 documents

Catalytic Dehydration of Fructose to 5-Hydroxymethylfurfural in Aqueous Medium over Nb2O5-Based Catalysts

2021

The catalytic dehydration of fructose to 5-hydroxymethylfurfural (HMF) in water was performed in the presence of pristine Nb2O5 and composites containing Nb and Ti, Ce or Zr oxides. In all experiments, fructose was converted to HMF using water as the solvent. The catalysts were characterized by powder X-ray diffraction, scanning electron microscopy, N2 physical adsorption, infrared and Raman spectroscopy and temperature-programmed desorption of NH3. Experimental parameters such as fructose initial concentration, volume of the reacting suspension, operation temperature, reaction time and amount of catalyst were tuned in order to optimize the catalytic reaction process. The highest selectivit…

General Chemical Engineeringtitanium oxide02 engineering and technologybiomass valorization010402 general chemistry01 natural sciencesArticle5-HMFCatalysisAutoclavechemistry.chemical_compoundAdsorptionbiomass valorization; 5-HMF; heterogeneous acid catalysis; niobium oxide; titanium oxide; green chemistryDesorptionGeneral Materials ScienceQD1-999green chemistryFructoseniobium oxide021001 nanoscience & nanotechnologyheterogeneous acid catalysis0104 chemical sciencesSolventChemistrychemistryYield (chemistry)0210 nano-technologySelectivityNuclear chemistryNanomaterials
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Photochemical sample treatment: a greener approach to chlorobenzene determination in sediments.

2014

Abstract Due to worker׳s exposure, solvent and stationary phases׳ consumption, sample purification is one of the most polluting steps in analytical procedures for determination of organic pollutants in real samples. The use of photochemical sample treatment represents a valid alternative methodology for extracts clean up allowing for a reduction of the used amount of organic solvents. In this paper we report the first application on the photolytic destruction of organic substances to eliminate some of the interferences in the analysis of Chlorobenzenes in sediment samples. The method׳s efficiency and robustness were compared with classic silica column purification process currently used in …

Geologic SedimentsPhotochemistryPhotochemistryChlorobenzenesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliGas Chromatography-Mass SpectrometryAnalytical ChemistrySpecimen Handlingchemistry.chemical_compoundLimit of DetectionSediment analysiClean upSoil PollutantsSettore CHIM/01 - Chimica Analiticasample treatmentPollutantDetection limitReproducibilityChromatographyChromatographySediment AnalysisPhotochemicalUV irradiationTemperatureReproducibility of ResultsWaterGreen Chemistry TechnologySettore CHIM/06 - Chimica OrganicaReplicateClean-upchemistryChlorobenzeneEnvironmental chemistrySolventsSediment analysisAnalytical proceduresChlorobenzeneTalanta
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DEEP EUTECTIC SOLVENTS E LIQUIDI IONICI: SOLVENTI PER LO SVILUPPO DI PROCESSI ECO-COMPATIBILI

2020

L’obiettivo di questi tre anni di Dottorato è stato lo studio e l’utilizzo nuovi solventi di reazione in grado di sostituire i solventi organici classici. In particolare sono stati studiati i Deep Eutectic Solvent (DES) e le miscele di Liquidi Ionici (IL). I DES sono stati utilizzati come solventi per lo studio di reazioni organiche, usate per la formazione di nuovi legami C-C. Nello specifico sono state studiate la reazione di Diels-Alder, e diverse reazioni di coupling C-C catalizzate da Pd. In seguito, i DES sono stati utilizzati per la formazione di nuovi gel supramolecolari, chiamati eutectogel. Questi gel sono stati formati usando come gelator amminoacidi naturali, consentendo quindi …

Green Chemistry Deep Eutectic Solvents Solventi Liquidi Ionici Eutectogel gel supramolecolari Diels-Alder solventi alternativi Reazione di accoppiamento C-C Reazione di Suzuki 5-HMF Biomasse Disidratazione di carboidrati Fruttosio Glucosio Saccarosio Processi Eco-compatibili.Settore CHIM/06 - Chimica OrganicaGreen Chemistry Deep Eutectic Solvents Solvents Ionic Liquids Eutectogel supramolecular gels Diels-Alder alternative solvents Cross Coupling Reaction Suzuki Reaction Sonogashira Reaction Heck Reaction Hiyama Reaction 5-HMF Biomass carbohydrate dehydration Fructose Glucose Saccarose.
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22nd International Scientific Conference “EcoBalt 2021”: Book of Abstracts (Riga, Latvia, October 21–23, 2021)

2021

The abstract book contains abstracts of the participants of the 22nd International Scientific Conference "EcoBalt 2021".

Green ChemistryPharmacy and Environment:NATURAL SCIENCES::Chemistry [Research Subject Categories]Environmental EducationEnvironmental ChemistrySustainable Chemistry and New Applied MaterialsAnalytical ChemistryFood safety
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Micro(Nano)plastic analysis: a green and sustainable perspective

2022

Within the last years aspects such as green, eco-friendly and sustainable are making their way into analytical chemistry. The field has changed with the introduction of these concepts. Information on the consumption of toxic solvents and energy is now a part of everyday life. This green analytical chemistry could be playing a pioneering role in the analysis of micro(nano)plastics in the environment. We discuss the roles of green analytical and sustainability within micro(nano) plastics determination and its possible applications. We explain its many advantages, like their function to preserve the environment and operator health or their role in the so-called eco-friendly methodologies, but …

Green chemistry principlesEnergy reductionMicroplasticsGreen analytical chemistry (GAC)Medi ambient ProteccióNanoplasticsJournal of Hazardous Materials Advances
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New Approach to 1,4-Benzoxazin-3-ones by Electrochemical C-H Amination.

2017

1,4-Benzoxazin-3-ones are important structural motifs in natural products and bioactive compounds. Usually the synthesis of benzoxazinones requires transition metal catalysts and pre-functionalized substrates, e.g. aryl halides. However, the anodic C,H amination of phenoxy acetates offers a very efficient and sustainable access to these heterocycles. The herein presented electrochemical protocol can be applied to a broad scope of alkylated substrates. Even tert-butyl moieties or halogen substituents are compatible with this versatile method.

Green chemistry010405 organic chemistryBenzoxazinonesArylOrganic ChemistryHalideGeneral ChemistryAlkylation010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryHalogenOrganic chemistryAminationChemistry (Weinheim an der Bergstrasse, Germany)
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Electrochemical Amination of Less-Activated Alkylated Arenes Using Boron-Doped Diamond Anodes

2016

The anodic C–H amination of aromatic compounds is a powerful and versatile method for the synthesis of aniline derivatives. By using boron-doped diamond (BDD) anodes, a method initially described by Yoshida et al. for electron-rich arenes was expanded to less-activated aromatic systems e.g., simple alkylated benzene derivatives. Anodes based on sp3 carbon seem to be the key for the electrochemical amination reaction. The corresponding primary anilines are obtained in good yields. Despite the cationic intermediates of the electrolytic reaction tert-butyl moieties are tolerated.

Green chemistry010405 organic chemistryChemistryOrganic ChemistryCationic polymerizationDiamondchemistry.chemical_elementengineering.materialAlkylation010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundAnilineengineeringOrganic chemistryPhysical and Theoretical ChemistryCarbonAminationEuropean Journal of Organic Chemistry
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Synthesis of Highly Functionalized N , N ‐Diarylamides by an Anodic C, N ‐Coupling Reaction

2019

We report an innovative, sustainable and straightforward protocol for the synthesis of N,N-diarylamides equipped with nonprotected hydroxyl groups by using electrosynthesis. The concept allows the application of various substrates furnishing diarylamides with yields up to 57 % within a single and direct electrolytic protocol. The method is thereby easy to conduct in an undivided cell with constant current conditions offering a versatile and short-cut alternative to conventional pathways.

Green chemistry010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryElectrolyte010402 general chemistryElectrosynthesisElectrochemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reaction0104 chemical sciencesAnodeConstant currentChemistry – A European Journal
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A Bipyridine‐Palladium Derivative as General Pre‐Catalyst for Cross‐Coupling Reactions in Deep Eutectic Solvents

2019

A versatile and DES‐compatible bipyridine palladium complex has been developed as a general pre‐catalyst for different cross‐coupling reactions (Hiyama, Suzuki‐Miyaura, Heck‐Mizoroki and Sonogashira) in deep eutectic solvents. Hydrogen bond capacity of the ligand allows to keep the excellent level of results previously obtained in classical organic solvents. Palladium pre‐catalyst showed a high catalytic activity for many cross‐coupling reactions, demonstrating a great versatility and applicability. Also, this methodology employs sustainable solvents as a reaction medium and highlights the potential of DES as alternative solvents in organometallic catalysis. The catalyst and DES were easily…

Green chemistry010405 organic chemistryHydrogen bondchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCoupling reaction0104 chemical sciencesCatalysisHydrogen bondsLigand designchemistry.chemical_compoundBipyridineQuímica OrgánicachemistryGreen chemistryPolymer chemistryCross-couplingDerivative (chemistry)PalladiumEutectic systemPalladium
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Electrochemical Synthesis of 5-Aryl-phenanthridin-6-one by Dehydrogenative N,C Bond Formation.

2018

Currently, the general synthesis of 5-aryl-phenanthridin-6-ones relies on the involvement of metal catalysis. Despite the urgent demand for green alternatives, avoiding synthetic routes that require transition metals for key roles is still challenging. Electrochemical efforts employing a constant potential protocol in divided cells revealed a possible alternative to the catalytic approach. A constant current protocol, undivided cells, and a remarkably low supporting electrolyte concentration enable a novel access to N-aryl-phenanthridin-6-ones by anodic N,C bond formation using directly generated amidyl radicals. Easy accessible starting materials, a broad scope of applicable functional gro…

Green chemistry010405 organic chemistrySupporting electrolyteArylRadicalOrganic ChemistryGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundTransition metalchemistryvisual_artvisual_art.visual_art_mediumChemistry (Weinheim an der Bergstrasse, Germany)
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