Search results for "Sorption"

showing 10 items of 4623 documents

Chemistry of Desiccant Properties of Carbohydrate Polymers as Studied by Near-Infrared Spectroscopy

2013

Published version of an article in the journal: Industrial and Engineering Chemistry Research. Also available from the publisher at: http://dx.doi.org/10.1021/ie302199k The combination frequency of water molecule in near-infrared spectroscopy is very useful for studying water molecular adsorption on solid surfaces. The absorption is purely from water molecules, and the variation in the absorption bands reflects the change in the environment of the water molecules on a surface. This variation, in turn, reflects the nature of the functional groups on the surface. Recently, Christy used this information in combination with second-derivative techniques to probe the surface of hydrothermally tre…

chemistry.chemical_classificationSilica gelGeneral Chemical EngineeringGeneral ChemistryPolymerVDP::Teknologi: 500::Kjemisk teknologi: 560Industrial and Manufacturing Engineeringchemistry.chemical_compoundAdsorptionChemical engineeringchemistryVDP::Matematikk og Naturvitenskap: 400::Kjemi: 440AmyloseAmylopectinPolymer chemistryMoleculeAbsorption (chemistry)SpectroscopyIndustrial & Engineering Chemistry Research
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Polymer-induced phase separation in suspensions of bacteria

2010

We study phase separation in suspensions of two unrelated species of rod-like bacteria, Escherichia coli and Sinorhizobium meliloti, induced by the addition of two different anionic polyelectrolytes, sodium polystyrene sulfonate or succinoglycan, the former being synthetic and the latter of natural origin. Comparison with the known behaviour of synthetic colloid-polymer mixtures and with simulations show that "depletion" (or, equivalently, "macromolecular crowding") is the dominant mechanism: exclusion of the non-adsorbing polymer from the region between two neighbouring bacteria creates an unbalanced osmotic force pushing them together. The implications of our results for understanding phe…

chemistry.chemical_classificationSinorhizobium melilotiADSORPTIONbiologyBiofilmMIXTURESfood and beveragesGeneral Physics and AstronomyPolymerAGGREGATIONbiology.organism_classificationmedicine.disease_causeLIGHT-SCATTERINGSUCCINOGLYCANPolyelectrolytechemistryESCHERICHIA-COLImedicineBiophysicsMacromolecular crowdingSodium Polystyrene SulfonateEscherichia coliBEHAVIORBacteriaEPL (Europhysics Letters)
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Carbon-based ionic liquid gels: alternative adsorbents for pharmaceutically active compounds in wastewater

2021

With the aim of obtaining adsorbent systems to be used for the removal of pharmaceutically active compounds (PhACs) from wastewater, some hybrid ionic liquid gels (HILGs) were obtained from the combination of ionic liquid-based supramolecular gels and carbon materials, like graphite, graphene and graphene oxide (graphene OX). The properties of HILGs were investigated by determining their gel–sol transition temperature and rheological features. They were tested for the removal of PhACs belonging to different pharmaceutical classes, like antibiotics, antidepressants, anti-inflammatory. In particular, the removal of carbamazepine (CBZ), diclofenac sodium salt (DCF), ciprofloxacin (CPX) and nal…

chemistry.chemical_classificationSorbentChemistryGrapheneMaterials Science (miscellaneous)OxideSalt (chemistry)PhAC removalSettore CHIM/06 - Chimica Organicalaw.inventionchemistry.chemical_compoundAdsorptionhybrid gelChemical engineeringWastewaterlawIonic liquidGraphiteGeneral Environmental Scienceionic liquidenvironmental remediation
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Sorption of Hydrocarbons on Peat, and Possibilities for Using Peat-Based Oil Sorbent for Treatment of Polluted Areas

2017

The growing use and transport of crude oil and oil products has led to an increasing amount of spillages of various scales. In the event of an oil spill, it is important to stop the spill from spreading and to clean up the polluted environment. One of the possible ways of treating the polluted areas is the use of oil sorbents. The sorbents used for collecting oil in case of oil spills are mostly synthetic, which limits the possibilities of their disposal. The aim of our study is to investigate the possible use of peat and its modification products for oil and other hydrocarbon sorption. Peat is a prospective material for oil sorption because it has such advantages as low cost, biodegradabil…

chemistry.chemical_classificationSorbentPeatHydrocarbonchemistrySpecific surface areaEnvironmental chemistryEnvironmental scienceSorptionBiodegradationPorositycomplex mixturesDecompositionLinnaeus Eco-Tech
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Consecutive Selective Adsorption of Pentamidine and Phosphate Biomolecules on a Self-Assembled Layer:  Reversible Formation of a Chemically Selective…

1996

In situ ellipsometric film thickness measurements, FT-IR external reflectance spectroscopy, and potentiometric measurements indicated that the amphiphile pentamidine (PAM), a bisbenzamidine, associated by self-assembly with a preformed self-assembled monolayer of a mercaptoalkanoic acid on gold. The structural properties of PAM and the nature of the substrate were ideal for the formation of a densely packed monolayer. This process was fully reversible, as demonstrated by changing the pH of the surrounding medium. Thus, disassembly−reassembly occurred when the pH was cycled between 8.7 and 3. The bilayer structure, featuring a positively charged amidinium surface, was subsequently used for s…

chemistry.chemical_classificationStereochemistryBilayerBiomoleculeSubstrate (chemistry)PhosphatePhotochemistryAnalytical Chemistrychemistry.chemical_compoundchemistrySelective adsorptionMonolayerAmphiphileSurface chargeAnalytical Chemistry
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Star-Shaped Compounds Having 1,3,5-Triazine Cores

2003

The 1,3,5-triazine derivatives 1−4 having styryl or higher oligo(phenylenevinylene) chains in the 2-, 4-, and 6-positions represent star-shaped push-pull compounds. Alkoxy or dimethylamino groups on the peripheral benzene rings, which act as electron donors, and the central 1,3,5-triazine ring, which acts as an electron acceptor, cause intramolecular charge transfer (ICT) to occur in the absorption S0⇄S1. Protonation of the 1,3,5-triazine core enhances the effect, as demonstrated by a bathochromic shift; a secondary protonation on the dimethylamino groups, however, leads to the breakdown of the ICT. Thus, the yellow compound 1d first becomes violet and then colorless upon the addition of tr…

chemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryProtonationElectron acceptorMedicinal chemistrychemistry.chemical_compound135-TriazineIntramolecular forceBathochromic shiftAlkoxy groupTrifluoroacetic acidPhysical and Theoretical ChemistryAbsorption (chemistry)European Journal of Organic Chemistry
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Mono and dinuclear copper(II) complexes of 2,4,6-tris(2-pyridyl)-1, 3,5-triazine and halide or pseudohalide ions: Synthesis and spectral studies

1986

By inhibiting the copper(II) assisted TPT (TPT = 2,4,6-tris(2-pyridyl)-1,3,5-triazine) hydrolysis, monomeric and dimeric copper(II) complexes having as general formulae Cu(TPT)X, · nH2O (X = Cl, Br, NCS, NCO or N3) and [Cu(TPT)X]2(PF6)2 · nH2O (X = Cl, Br, NCS or N3) have been synthesized and characterized by i.r., electronic and e.p.r. spectra, x-ray powder diffraction and analytical data. Spectroscopic results indicate five-coordinate geometry around the copper(II) ion, intermediate between trigonal-bipyramid and square-pyramid structures. The half-field absorption in the ΔMS = 2 region of powdered X-band e.p.r. spectra has been observed for the dimeric species.

chemistry.chemical_classificationStereochemistryMetals and AlloysHalidechemistry.chemical_elementCopperInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistry135-TriazineMaterials ChemistryAbsorption (chemistry)Inorganic compoundOrganometallic chemistryPowder diffractionTransition Metal Chemistry
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Conjugated Oligomers with Terminal Donor–Acceptor Substitution

2005

Conjugated oligomers represent a prominent class of compounds from a viewpoint of their theory, synthesis, and applications in materials science. Push-pull substitution with an electron donor D at one end of the conjugation and an electron acceptor A at the other end results in them having outstanding optical and electronical properties. This Review highlights fundamental synthetic strategies for the preparation of such oligomers with n repeat units (n=1, 2, 3, 4, ..) and the rules that govern their linear and nonlinear optical properties (absorption, frequency doubling and tripling). The unification of chemical, physical, and theoretical aspects with an interdisciplinary image of this clas…

chemistry.chemical_classificationStereochemistrySubstitution (logic)Nonlinear opticsElectron donorGeneral MedicineGeneral ChemistryConjugated systemElectron acceptorCombinatorial chemistryCatalysisNonlinear opticalchemistry.chemical_compoundchemistryTerminal (electronics)Absorption (chemistry)Donor acceptorAngewandte Chemie International Edition
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Molecular modeling studies of interactions between styrene–butadiene latex and sodium polyacrylate polymer surface

2010

Abstract The interaction between two important paper coating ingredients, sodium polyacrylate polymer dispersing agent and styrene–butadiene latex binder, was studied using classical force field and quantum chemical methods. The objective was to understand the adsorption of styrene–butadiene latex on the sodium polyacrylate polymer model surfaces at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree–Fock method was also used to obtain detailed information about the above interactions. In addition, the effect of moisture was investigated. Calculations showed that the conformation and orientation of styrene–butadiene latex, the number of carboxylate groups in t…

chemistry.chemical_classificationStyrene-butadieneSodium polyacrylateSodiumchemistry.chemical_elementPolymerCondensed Matter PhysicsBiochemistryDispersantchemistry.chemical_compoundMolecular dynamicsAdsorptionchemistryPolymer chemistryMoleculePhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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Oxidation of Sulfides with a Silica-Supported Peracid in Supercritical Carbon Dioxide under Flow Conditions: Tuning Chemoselectivity with Pressure

2010

Supercritical carbon dioxide is a convenient medium for performing the selective oxidation of sulfides 1 to either sulfoxides 2 or sulfones 3 with [2-percarboxyethyl]-functionalized silica (4) under flow conditions. The chemoselectivity of the reaction, which results from the different diffusion rates of sulfide and sulfoxide over the reagent bed, can be controlled by adjusting the pressure and the hydration of the silica surface as both the solvating power of the mobile phase and the surface activity of the stationary phase determine the migration rates of sulfide 1 and sulfoxide 2 over the supported peroxide. The results elucidate the impact of surface phenomena on the course of chemical …

chemistry.chemical_classificationSupercritical carbon dioxideSulfideChemistryOrganic ChemistryInorganic chemistrySulfoxideChemical reactionSupercritical fluidchemistry.chemical_compoundAdsorptionReagentPhysical and Theoretical ChemistryChemoselectivityEuropean Journal of Organic Chemistry
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