Search results for " Solvents"

showing 10 items of 35 documents

Species- and site-specific efficacy of commercial biocides and application solvents against lichens

2017

Abstract Control of lichens on stone cultural heritage is mostly achieved by a combination of mechanical removal with biocide applications. However, there is a lack of scientific evidence on the efficacy of different biocides on different species, and on the consistency of biocide effects on heritage sites in different environmental conditions. This results in some uncertainty when conservation interventions to control lichens are routinely defined on the basis of restoration tradition or empirical evaluation, without experimental measures of how lichens respond. In this work, we quantitatively evaluated (a) the efficacy of five commercially-available biocides, applied using a brush or with…

0301 basic medicineBiocideBiocide; Chlorophyll a fluorescence; Ergosterol; Lichen; Organic solvents; Microbiology; Biomaterials; Waste Management and DisposalBiocide030106 microbiologyLichenVerrucaria nigrescens010501 environmental sciencesBiologyVitalityProtoparmeliopsis muralis01 natural sciencesMicrobiologyBiomaterials03 medical and health sciencesErgosterolChlorophyll a fluorescenceBotanyLichenWaste Management and Disposal0105 earth and related environmental sciencesBiocide Chlorophyll fluorescence Ergosterol Lichen Organic solventsPoulticeOrganic solventsEnvironmental chemistryChlorophyll fluorescenceBiocide Chlorophyll a fluorescence Ergosterol Lichen Organic solventsInternational Biodeterioration & Biodegradation
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The effect of organic solvents on selected microorganisms and model liposome membrane

2019

The effect of methanol, ethanol, acetone, N,N-dimethylformamide (DMF), dimethyl sulfoxide and Nujol on the growth of Escherichia coli DH5α, Bacillus subtilis and Saccharomyces cerevisiae D273 was investigated. All of the tested cultures appeared susceptible to the organic media they were treated with, which evinced in apparent hindering of cell development. The observed diverse solvent tolerance, except from their different biochemical activity, may also be related to the changes in cell membrane fluidity induced by the solvent species. Parallel electron paramagnetic resonance investigations using egg yolk lecithin model liposomes revealed that the fluidity of the phospholipid system in cel…

0301 basic medicinefood.ingredientPhospholipidLecithin03 medical and health scienceschemistry.chemical_compound0302 clinical medicinefoodElectron paramagnetic resonance (EPR)GeneticsAcetoneMembrane fluidityorganic solventsOrganic ChemicalsMolecular BiologyChromatographyBacteriaMolecular StructureDimethyl sulfoxideCell MembraneElectron Spin Resonance SpectroscopyGeneral MedicineYeastSolvent030104 developmental biologyMembranechemistryNujol030220 oncology & carcinogenesisLiposomesSolventsMolecular Biology Reports
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Peak half-width plots to study the effect of organic solvents on the peak performance of basic drugs in micellar liquid chromatography.

2009

The addition of the anionic surfactant sodium dodecyl sulphate (SDS) to hydro-organic mixtures of methanol, ethanol, propanol or acetonitrile with water yielded enhanced peak shape (i.e. increased efficiencies and symmetrical peaks) for a group of basic drugs (β-blockers) chromatographed with a Kromasil C18 column. The effect can be explained by the thin layer of surfactant associated to the hydrocarbon chain on the stationary phase in the presence of the organic solvents, which covers the free silanols on the siliceous support avoiding their interaction with the cationic basic drugs. These instead interact with the anionic head of the surfactant increasing their retention and allowing a mo…

AcetonitrilesInorganic chemistryAdrenergic beta-AntagonistsBiochemistryMicelleAnalytical ChemistryPropanolchemistry.chemical_compoundPulmonary surfactantBasic compoundsSodium dodecyl sulphatePeak performanceSodium dodecyl sulfateAcetonitrileMicelleschemistry.chemical_classificationChromatographyOrganic ChemistrySodium Dodecyl SulfateGeneral MedicineOrganic solventsHydrocarbonchemistryMicellar liquid chromatographyAlcoholsLinear Modelsβ-BlockersMethanolMicellar liquid chromatographyPeak half-widthsChromatography LiquidJournal of chromatography. A
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Effect of Stiffness on the Micellization Behavior of Model H4T4 Surfactant Chains

2006

The micellization behavior of a series of model surfactants, all with four head and tail groups (H4T4) but with different degrees of chain stiffness, was studied using grand canonical Monte Carlo simulations on a cubic lattice. The critical micelle concentration, micellar size, and thermodynamics of micellization were examined. In all cases investigated, the critical micelle concentration was found to increase with increasing temperature as observed for nonionic surfactants in apolar or slightly polar solvents. At a fixed reduced temperature and increasing chain stiffness, in agreement with previous observations, it was found that the critical micelle concentration decreased and the average…

Aggregation numberChemistryCrystal lattices Hydrophobicity Micelles Molecular structure Monte Carlo methods SolventsThermodynamics of micellizationMonte Carlo methodtechnology industry and agricultureThermodynamicsSurfaces and InterfacesCondensed Matter PhysicsMicelleSurface-Active AgentsReduced propertiesPulmonary surfactantCritical micelle concentrationElectrochemistryThermodynamicsOrganic chemistryPolarGeneral Materials ScienceMonte Carlo MethodMicellesSpectroscopySettore CHIM/02 - Chimica FisicaLangmuir
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Application of a low transition temperature mixture for the dispersive liquid–liquid microextraction of illicit drugs from urine samples

2021

© 2021 by the authors.

BioanalysisLiquid Phase MicroextractionProductes biològicsIllicit drugsDispersive liquid–liquid mi-croextractionPharmaceutical ScienceOrganic chemistryUrineUrineHigh-performance liquid chromatographyBiological samples; Deep eutectic solvents; Dispersive liquid–liquid mi-croextraction; Drugs; High performance liquid chromatography; Illicit drugs; Low transition temperature mixtures; UrineArticleLow transition temperature mixturesAnalytical Chemistrychemistry.chemical_compoundBiological samplesQD241-441Limit of DetectionDrug DiscoveryHumansTransition TemperatureSample preparationPhysical and Theoretical ChemistryChromatographyChemistryExtraction (chemistry)Deep eutectic solventsDrugsSolventCold TemperatureChemistry (miscellaneous)Dispersive liquid–liquid microextractionMolecular MedicineDroguesGlass transitionCholine chlorideHigh performance liquid chromatography
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DFT calculation of 1J(119Sn,13C) and 2J(119Sn,1H) coupling constants in di- and trimethyltin(IV) compounds

2008

We have tested several computational protocols, at the nonrelativistic DFT level of theory, for the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) spin-spin coupling constants in di- and trimethyltin(IV) derivatives with various ligands. Quite a good agreement with experimental data has been found with several hybrid functionals and a double-zeta basis set for a set of molecules comprising tetra-, penta-, and hexa-coordinated tin(IV). Then, some of the protocols have been applied to the calculation of the 2J(119Sn, 1H) of the aquodimethyltin(IV) ion and dimethyltin(IV) complex with D-ribonic acid and to the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) of the dimethyltin(IV)-glycylglycin…

Carbon Isotopes; Dipeptides; Glycylglycine; Hydrogen; Organotin Compounds; Solvents; Tin; Trimethyltin Compounds; Water; Quantum Theorychemistry.chemical_elementInorganic ChemistryOrganotin(IV) DFT NMR relativistic effects tin couplingsComputational chemistryOrganotin CompoundsMoleculePhysical and Theoretical ChemistryBasis setCoupling constantCarbon IsotopesNMR tin derivatives coupling constantsTrimethyltin CompoundsbiologyGlycylglycineWaterDipeptidesbiology.organism_classificationHybrid functionalSolventchemistryTinSolventsQuantum TheoryTetraSolvent effectsTinHydrogen
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EVALUATION OF AEROBIC AND ANAEROBIC BACTERIAL DECHLORINATION POTENTIAL OF A 1,2-DICHLOROETHANE CONTAMINATED AQUIFER

2023

Chlorinated solvents, belonging to the class of chlorinated aliphatic hydrocarbons (CAHs), are synthetic organohalide chemicals frequently found as contaminants of groundwater and soil, due to their widespread use in several industrial processes and improper disposal methods. These compounds pose serious health threats because of their toxic and sometimes carcinogenic effects. Among these compounds, 1,2-dichloroethane (1,2-DCA) is one of the most common aquifer contaminants, considered toxic and classified as a possible human carcinogen. Remediation approaches toward these contaminants include conventional cleanup technologies based on physical/chemical methods, and bioremediation, consider…

Chlorinated solvents12-dichloroethaneSettore BIO/19 - Microbiologia GeneraleBioremediationBacterial communities
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Solubility and solvation features of native cyclodextrins in 1-ethyl-3-methylimidazolium acetate

2022

The comprehension of the mechanism entailing efficient solvation of cyclodextrins (CD) by green solvents is of great relevance to boost environmentally sustainable usages of smart supramolecular systems. Here, 1-ethyl-3- methylimidazolium acetate, an ecofriendly ionic liquid (IL), is considered as an excellent solvent for native CDs. This IL efficiently dissolves up to 40 wt.% β- and γ-CD already at ambient temperature and X-ray scattering indicates that CDs do not tend to detrimental flocculation under these drastic concentration conditions. Simu- lation techniques reveal the intimate mechanism of CD solvation by the ionic species: while the strong hydrogen bonding acceptor acetate anion i…

CyclodextrinsPolymers and Plasticscyclodextringreen chemistrysolubilityOrganic ChemistryIonic liquids Solvation Hydrophobic solvation Cyclodextrin Emerging task specific solvents Sustainability Molecular dynamics Hydrogen bondingMaterials ChemistryImidazolesSolventsiONIC lIQUIDS cyclodextrin solubility green chemistryiONIC lIQUIDSSettore CHIM/02 - Chimica Fisica
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L'AZIONE COMBINATA DES/ULTRASUONI PER LO STUDIO DELLA REAZIONE DI DIELS-ALDER

DEEP EUTECTIC SOLVENTS ULTRASUONI REAZIONE DI DIELAS ALDERSettore CHIM/06 - Chimica Organica
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Conversion of carbohydrates into 5-HMF in Deep Eutectic Solvents under mild reaction conditions

Deep eutectic solvents carbohydrate conversion 5-hydroxymethylfurfural biomass valorization environmental friendly processSettore CHIM/06 - Chimica Organica
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