Search results for "supporting"

showing 10 items of 82 documents

Metal-free electrochemical fluorodecarboxylation of aryloxyacetic acids to fluoromethyl aryl ethers

2020

Electrochemical decarboxylation of aryloxyacetic acids followed by fluorination provides easy access to fluoromethyl aryl ethers. This electrochemical fluorodecarboxylation offers a sustainable approach with electric current as traceless oxidant. Using Et3N·5HF as fluoride source and as supporting electrolyte, this simple electrosynthesis affords various fluoromethoxyarenes in yields up to 85%.

Chemistrychemistry.chemical_compoundchemistryMetal freeSupporting electrolyteDecarboxylationArylGeneral ChemistryElectrochemistryElectrosynthesisCombinatorial chemistryFluorideChemical Science
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Abatement of Acid Orange 7 in macro and micro reactors. Effect of the electrocatalytic route

2014

Abstract The electrochemical treatment of aqueous solutions contaminated by Acid Orange 7 (AO7) was widely studied with the main objective to evaluate as the electrocatalytic route affects the performances of the degradation process in macro and microfluidic cells. Direct anodic oxidation (EO), electro-Fenton (EF), electro-generation of active chlorine (IOAC) and coupled processes were investigated in macro and microfluidic reactors in order to select more effective conditions for the treatment of such compound. The effect of numerous operative parameters (such as nature of the electrode materials, coupling of processes, flow rate, current density and inter-electrode distance) on the perfor…

ChromatographyAqueous solutionSupporting electrolyteChemistryProcess Chemistry and TechnologyElectrocatalysiElectrochemistryElectrocatalystCatalysisCatalysisVolumetric flow rateChemical engineeringMass transferActive chlorineAcid Orange 7Electro-FentonMicroreactorMicro reactorBDDGeneral Environmental Science
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Determination of rate constants of ion transfer kinetics across immiscible electrolyte solutions

1998

Abstract The rotating diffusion cell was used to study ion transfer across the interface between two immiscible electrolyte solutions. Tetrabutylammonium was chosen as the transferring cation and lithium chloride as the supporting electrolyte in aqueous phase. Tetrabutylammonium tetrakis-(4-fluorophenyl)-borate in 2-nitrophenyl-octylether was used as the organic electrolyte solution supported in the porous membrane. The quasi-steady state current–voltage curves were measured both by applying potential steps and by imposing a slow potential sweep. The analysis of experimental results was based on the comparison with the theoretical current–voltage curves and on the Koutecky–Levich plots. The…

ChromatographySupporting electrolyteGeneral Chemical EngineeringAqueous two-phase systemThermodynamicsConcentration effectElectrolytechemistry.chemical_compoundReaction rate constantElectrical resistance and conductancechemistryElectrochemistryLithium chlorideITIESElectrochimica Acta
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Towards a design process for modeling MAS organizations

2012

The design of MAS organizations is a complex activity where a proper methodological approach may offer a significant advantage in enabling the conception of the best solution. Moreover, the aid provided by a supporting tool significantly contributes to make the approach technically sound and it is a fundamental ingredient of a feasible strategy to the development of large MASs. In this paper, we introduce a portion of methodological approach devoted to design MAS organizations and a preliminary version of a specific case tool, named MoT (Moise+ Tool), for supporting activities from design production to automatic code generation. MoT provides four kinds of diagrams based on a definite graphi…

Computer sciencebusiness.industryProcess (engineering)NotationGraphical notationMethodological approachDevelopment (topology)Complex activityCode (cryptography)Design processProduction (economics)Code generationArtificial intelligenceAutomatically generatedDesign proceSoftware engineeringbusinessComputer-aided software engineeringSupporting toolAutomatic code generation
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Cathodic reduction of hexavalent chromium coupled with electricity generation achieved by reverse-electrodialysis processes using salinity gradients

2014

Abstract A new approach for the simultaneous generation of electric energy and the treatment of waters contaminated by recalcitrant pollutants using salinity gradients was proposed. Reverse electrodialysis allows for the generation of electric energy from salinity gradients. Indeed, the utilization of different salt concentrations gives a potential difference between the electrodes which allows the generation of electric energy by using suitable electrolytes and an external circuit. The simultaneous generation of electric energy and the treatment of waters contaminated by Cr(VI) was successfully achieved for the first time by reverse electrodialysis processes using salinity gradients and pr…

Cr(VI)ChemistrySupporting electrolyteGeneral Chemical EngineeringElectrolytesalinity gradientVolumetric flow rateSalinitychemistry.chemical_compoundElectricity generationChemical engineeringStack (abstract data type)Waste water treatmentenergy generationEnvironmental chemistryReversed electrodialysisElectrochemistryreverse electrodialisyHexavalent chromium
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Meeting the Challenges of Generational Change in the Teaching Profession : Towards a European Model for Intergenerational Teacher Collaboration

2013

In a European-wide effort to improve the professional development of teachers, the 2AgePro project was conducted from November 2008 to October 2010. One of its goals was to develop and test different forms of intergenerational teacher collaboration among junior and senior teachers in primary and secondary schools. Another aim was to utilise the results from these pilots, which were conducted in the Czech Republic, Finland, Germany, the Netherlands, and Sweden, to create a model for intergenerational collaboration that could be used in any national or cultural setting. This article reports on the national pilots and proposes a European model for intergenerational collaboration for teachers. …

Czechjunior teacherPedagogyProfessional developmentPedagogikContinuing educationCollaborative learningTeacher learningsenior teachersupporting systemlanguage.human_languageTest (assessment)Collaborative learningcollaboration scriptsSupporting systemDidáctica y Organización EscolarPolitical scienceteacher learningPedagogycontinuing educationlanguage
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BioTIME: A database of biodiversity time series for the Anthropocene

2018

Abstract Motivation The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community-led open-source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene. Main types of variables included The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, th…

Data Papers0106 biological sciencesRange (biology)QH301 BiologytemporalNERCBiodiversity:Matematikk og Naturvitenskap: 400::Zoologiske og botaniske fag: 480 [VDP]BIALOWIEZA NATIONAL-PARKspecialcomputer.software_genre[SDV.BID.SPT]Life Sciences [q-bio]/Biodiversity/Systematics Phylogenetics and taxonomy01 natural sciencesspecies richnessSDG 15 - Life on LandbiodiversityGlobal and Planetary ChangeB003-ecologyDatabaseEcologySampling (statistics)SIMULATED HERBIVORYsupporting technologiesLAND-BRIDGE ISLANDS[SDV.BV.BOT]Life Sciences [q-bio]/Vegetal Biology/BotanicsPE&RCglobal/dk/atira/pure/thematic/inbo_th_00032PRIMEVAL TEMPERATE FORESTGeographyPOPULATION TRENDS/dk/atira/pure/discipline/B000/B003biodiversity; global; special; species richness; temporal; turnoverData PaperSECONDARY FORESTEvolutionESTUARINE COASTAL LAGOON010603 evolutionary biology/dk/atira/pure/sustainabledevelopmentgoals/life_below_waterQH301[SDV.EE.ECO]Life Sciences [q-bio]/Ecology environment/EcosystemsBehavior and SystematicsAnthropocenebiodiversity; global; spatial; species richness; temporal; turnover; Global and Planetary Change; Ecology Evolution Behavior and Systematics; EcologyVDP::Mathematics and natural science: 400::Zoology and botany: 480species richne14. Life underwaterSDG 14 - Life Below WaterNE/L002531/1ZA4450Relative species abundanceEcology Evolution Behavior and SystematicsZA4450 Databases010604 marine biology & hydrobiologyturnoverRCUKBiology and Life SciencesDAS/dk/atira/pure/technological/ondersteunende_technieken15. Life on landDECIDUOUS FORESTspatialTaxonFish13. Climate actionMCPWildlife Ecology and ConservationLONG-TERM CHANGESpecies richness[SDE.BE]Environmental Sciences/Biodiversity and EcologycomputerGlobal and Planetary ChangeBIRD COMMUNITY DYNAMICSVDP::Matematikk og Naturvitenskap: 400::Zoologiske og botaniske fag: 480
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Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups

2019

Abstract We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans.

Denticityoxidation010405 organic chemistryChemistrySupporting electrolyteCommunicationC−C couplingoxygen heterocyclesSubstrate (chemistry)General Chemistry010402 general chemistryElectrochemistry01 natural sciencesEnvironmentally friendlyCombinatorial chemistryCommunicationsCatalysisCoupling reaction0104 chemical scienceschemistry.chemical_compoundElectrochemistry | Hot Paperelectrochemistrycross-couplingPolar effectPhenolsAngewandte Chemie International Edition
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Electrochemical impedance spectroscopy of thin films with two mobile charge carriers: effects of the interfacial charging

1999

In the electrochemical systems containing an excess of the background electrolyte, the faradaic process and the interfacial (‘double-layer’) charging are coupled to the fluxes of different charge carriers, the former being related to the diffusional transport of electroactive entities while the latter being realized mostly by ions of the supporting electrolyte. As a result, the interfacial capacitance Cdl may simply be added in parallel to the faradaic impedance specific for each particular system (Randles & Ershler). This simple treatment is not justified in the absence of an indifferent electrolyte, if the same charged species take part in both the electrode reaction and the double layer …

Double layer (biology)ChemistrySupporting electrolyteGeneral Chemical EngineeringFaradaic impedanceAnalytical chemistryElectrolyteConductivityAnalytical ChemistryDielectric spectroscopyIonChemical physicsElectrochemistryCharge carrierJournal of Electroanalytical Chemistry
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Supporting-Electrolyte-Free and Scalable Flow Process for the Electrochemical Synthesis of 3,3′,5,5′-Tetramethyl-2,2′-biphenol

2020

The most efficient electrochemical synthesis of 3,3′,5,5′-tetramethyl-2,2′-biphenol by dehydrogenative coupling is reported. The electrolysis is performed supporting-electrolyte-free in 1,1,1,3,3,3...

ElectrolysisMaterials science010405 organic chemistrySupporting electrolyteOrganic ChemistryFlow cell010402 general chemistryElectrochemistry01 natural sciences0104 chemical scienceslaw.inventionCoupling (electronics)Chemical engineeringlawPhysical and Theoretical ChemistryFlow processOrganic Process Research & Development
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