Search results for "SOLVENT"

showing 10 items of 1395 documents

Salt-induced microheterogeneities in binary liquid mixtures

2017

The salt-induced microheterogeneity (MH) formation in binary liquid mixtures is studied by small-angle x-ray scattering (SAXS) and liquid state theory. Previous experiments have shown that this phenomenon occurs for antagonistic salts, whose cations and anions prefer different components of the solvent mixture. However, so far the precise mechanism leading to the characteristic length scale of MHs has remained unclear. Here, it is shown that MHs can be generated by the competition of short-ranged interactions and long-ranged monopole-dipole interactions. The experimental SAXS patterns can be reproduced quantitatively by fitting to the derived correlation functions without assuming any speci…

Chemical Physics (physics.chem-ph)Phase transitionSpinodalMaterials scienceCharacteristic lengthCondensed Matter - Mesoscale and Nanoscale PhysicsSmall-angle X-ray scatteringScatteringThermodynamicsFOS: Physical sciences02 engineering and technologyCondensed Matter - Soft Condensed Matter010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSolventCondensed Matter::Soft Condensed MatterIonic strengthPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Soft Condensed Matter (cond-mat.soft)0210 nano-technologyPhase diagram
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Computer simulation of bottle-brush polymers with flexible backbone: good solvent versus theta solvent conditions.

2011

By Molecular Dynamics simulation of a coarse-grained bead-spring type model for a cylindrical molecular brush with a backbone chain of $N_b$ effective monomers to which with grafting density $\sigma$ side chains with $N$ effective monomers are tethered, several characteristic length scales are studied for variable solvent quality. Side chain lengths are in the range $5 \le N \le 40$, backbone chain lengths are in the range $50 \le N_b \le 200$, and we perform a comparison to results for the bond fluctuation model on the simple cubic lattice (for which much longer chains are accessible, $N_b \le 1027$, and which corresponds to an athermal, very good, solvent). We obtain linear dimensions of …

Chemical Physics (physics.chem-ph)chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceCharacteristic lengthTheta solventFOS: Physical sciencesGeneral Physics and AstronomyBackbone chainPolymerCondensed Matter - Soft Condensed MatterPower lawCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicschemistryChemical physicsPhysics - Chemical PhysicsSide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistrySolvent effectsThe Journal of chemical physics
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Determination of bisphenol diglycidyl ether residues in canned foods by pressurized liquid extraction and liquid chromatography–tandem mass spectrome…

2005

Abstract A new confirmatory method for simultaneous determination of bisphenol diglycidyl ether residues (BADGE, BADGE·H2O, BADGE·2H2O, BADGE·H2O·HCl, BADGE·HCl, BADGE·2HCl, BFDGE and BFDGE·2HCl) from canned food has been developed. The proposed method includes extraction by pressurized liquid extraction (PLE) followed by liquid–liquid partition and purification by solid phase extraction (SPE). Several solvent systems and different operating conditions (time, temperature) have been investigated for PLE optimization. A reversed-phase high-performance liquid chromatography (RP-HPLC) coupled to atmospheric pressure chemical ionisation tandem mass spectrometry (APCI-MS–MS) method was developed …

Chemical ionizationDiglycidyl etherChromatographyBisphenolOrganic ChemistryTemperatureAtmospheric-pressure chemical ionizationGeneral MedicineBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundAtmospheric PressurechemistryLiquid chromatography–mass spectrometrySolventsEpoxy CompoundsSolid phase extractionBenzhydryl CompoundsBisphenol A diglycidyl etherChromatography High Pressure LiquidFood AnalysisJournal of Chromatography A
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A joint action of deep eutectic solvents and ultrasound to promote Diels−Alder reaction in a sustainable way

2020

The need to reduce environmental impact of chemical processes has induced a surge of attention in the choice of solvent and methodologies to carry them out. In this context, we studied the Diels−Alder reaction using N-ethylmaleimide as dienophile and changing the nature of the diene in deep eutectic solvents (DES) under both conventional heating and ultrasonic activation. DES obtained by the combination of different hydrogen bond acceptors and donors allowed assessing the role played by solvent nature. DES proved suitable solvent media for the target reaction, allowing higher yields and faster reactions compared to conventional organic solvents. The trend of yields, both in silent and under…

Chemical processDeep eutectic solventMaterials scienceGeneral Chemical EngineeringContext (language use)02 engineering and technologySolvent effect010402 general chemistry01 natural sciencesRecyclabilityEnvironmental ChemistryUltrasound irradiationEutectic systemDiels–Alder reactionUltrasound irradiationRenewable Energy Sustainability and the EnvironmentfungiGeneral ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesJoint actionDiels−Alder reactionBiochemical engineeringSolvent effects0210 nano-technology
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Ionic liquids: “normal” solvents or nanostructured fluids?

2021

Ionic liquids (ILs) are a class of non-conventional solvents, which, for almost two decades, have continued to generate burgeoning interest in different fields of present-day chemical research with few similar precedents. Among the various aspects related to ILs, a topic worthy of in-depth analysis is their influence on organic reactivity and reaction rates. In light of this, the present short review aims to provide an overview of the literature from 2010 to the present day that addresses this issue. In particular, we herein present two main different viewpoints by which the solvent effect of ILs is explained: the first is mainly based on considering the bulk polarity of ILs and linear solv…

Chemical researchPolymer scienceChemistryPolarity (physics)Organic ChemistrySolvationorganic reactivityLSERSettore CHIM/06 - Chimica OrganicaIonic liquidBiochemistrychemistry.chemical_compoundIonic liquidReactivity (chemistry)Physical and Theoretical ChemistrySolvent effectsSupramolecular catalysis
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Molecular precursors of mesostructured silica materials in the atrane route: A DFT/GIAO/NBO theoretical study

2007

Abstract Quantum chemical calculations using density functional theory have been carried out to investigate two assumed molecular precursors and identified as silatranes (N[OCH2CH2]3Si–OCH2CH2N–(CH2CH2OH)2 and N[OCH2CH2]3Si–OCH2CH2N–(CH2CH2OH)2Na+) which are present in the synthesis of mesoporous silica based material namely “the atrane route”. One of the ways in this synthesis leads to the well-known MCM-41. Additionally, in this work has been also investigated two others molecules such as triethanolamine (TEAH3) and sodatrane which are present in the medium. Gas phase and solution equilibrium geometries of the previous molecules were fully optimized at B3LYP level, modeling solvent effect…

Chemical shiftCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundSolvation shellAtranechemistryComputational chemistryMoleculeDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsBasis setNatural bond orbitalJournal of Molecular Structure: THEOCHEM
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Comparison of thermal‐ and photo‐polymerization of lauryl methacrylate monolithic columns for CEC

2009

Lauryl methacrylate-based (LMA) monolithic columns for CEC, prepared using either thermal initiation or by UV-irradiation in the presence of AIBN have been compared. Thermal polymerization was carried out at 70 degrees C for 20 h. For UV initiation, the effects of the time exposure to UV light and irradiation energy were investigated. For each initiation process, the influence of composition of porogenic solvent (1,4-butanediol/1-propanol ratio) on the physical and electrochromatographic properties of the resulting monoliths was also evaluated. Photochemically lauryl methacrylate stationary phases initiated showed higher permeabilities and better efficiencies than those prepared by thermal …

Chemical substanceChromatographyMaterials scienceClinical BiochemistryBiochemistryAnalytical Chemistrylaw.inventionSolventMagazinePolymerizationlawPermeability (electromagnetism)ThermalIrradiationScience technology and societyNuclear chemistryELECTROPHORESIS
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Clean method for the simultaneous determination of propyphenazone and caffeine in pharmaceuticals by flow injection Fourier transform infrared spectr…

1997

A procedure is proposed for the simultaneous FTIR determination of propyphenazone (PFZ) and caffeine (CAF) in pharmaceuticals. The method involves the dissolution of the active principles in CHCl 3 , followed by filtration of sample solutions to remove the excipients. PFZ is then determined by absorbance measurements at 1595 cm - 1 , using a baseline established between 2000 and 890 cm - 1 , and CAF by using the first-derivative values at 1712 cm - 1 , using solutions of PFZ and CAF for external calibration. The method was applied in both the stopped-flow and flow-injection modes, providing precise and accurate results for the analysis of real samples. The incorporation of a distillation un…

ChemistryChemistry PharmaceuticalAnti-Inflammatory Agents Non-SteroidalAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical Chemistrylaw.inventionSolventAbsorbancelawCaffeineSpectroscopy Fourier Transform InfraredElectrochemistrymedicineSolventsEnvironmental ChemistryFourier transform infrared spectroscopyDissolutionPropyphenazoneDistillationSpectroscopyFiltrationAntipyrinemedicine.drugThe Analyst
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Fourier transform infrared analysis of paint solvents

1991

Abstract The composition of solvent mixtures employed in the paint industry was determined by Fourier transform infrared spectrometry. A procedure based on the use of the ratio between the absorbance of characteristic bands of each component permits the ratio between two solvents in a binary mixture to be determined, independently of the thickness of the sample film. Typical mixtures of xylol with butan-1-ol and with butyl acetate (xylol=mixture of o-, m- and p-xylenes) were used as model systems to develop the proposed procedure and the accuracy was determined using synthetic formulations. Another possible application of the procedure is the characterization of azeotropic mixtures.

ChemistryComponent (thermodynamics)InfraredAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistrySolventAbsorbancechemistry.chemical_compoundsymbols.namesakeFourier transformsymbolsEnvironmental ChemistryFourier transform infrared spectrometryButyl acetateSpectroscopyAnalytica Chimica Acta
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Determination of association constants towards carbon nanotubes

2015

Single-walled carbon nanotubes (SWNTs) are one of the most promising nanomaterials and their supramolecular chemistry has attracted a lot of attention. However, despite well over a decade of research, there is no standard method for the quantification of their noncovalent chemistry in solution/suspension. Here, we describe a simple procedure for the determination of association constants (Ka) between soluble molecules and insoluble and heterogeneous carbon nanotube samples. To test the scope of the method, we report binding constants between five different hosts and two types of SWNTs in four solvents. We have determined numeric values of Ka in the range of 1–104 M−1. Solvent effects as wel…

ChemistryComputational chemistrylawSupramolecular chemistryOrganic chemistryMoleculeGeneral ChemistryCarbon nanotubeSolvent effectsSuspension (chemistry)Nanomaterialslaw.invention
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