Search results for "Fractionation"

showing 10 items of 332 documents

The Efficiency of Polymer Fractionation at Lower Critical Solution Temperatures

1978

The efficiency of a single fractionation step (i.e. of the partition of a given polymer sample between the coexisting phases which form when its solution demixes) is governed by the variation of the mass ratio of the individual P-mers with chain length. These dependences have been measured for the system dimethoxymethane/diethylether/ polystyrene which exhibits lower critical solution temperatures by means of the Baker-Williams method and by means of g.p.c. Their comparison with the results of previous investigation on systems showing upper critical solution temperatures reveals no thermodynamic differences in the aptitude of upper and lower critical solution temperatures for fractionation …

chemistry.chemical_classificationPartition coefficientchemistryUpper critical solution temperaturePhase (matter)General EngineeringMolar mass distributionThermodynamicsGeneral Materials ScienceFractionationPolymerPolymer fractionationLower critical solution temperatureBritish Polymer Journal
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Chemical speciation of polycyclic aromatic hydrocarbons in sediments: partitioning and extraction of humic substances.

2010

The primary objective of this study was to examine the chemical speciation of polycyclic aromatic hydrocarbons (PAHs) found in sediments endowed with different characteristics. To achieve this purpose and because the nature of the sediments influences the distribution of PAHs, we have analyzed four different types of sediments. To study the role of organic matter in the sequestration of PAHs, we fractionated humic substances into humic acids and humin–mineral fractions. After their separation and purification, the humic components were examined for their sorptive reactivity by extracting them with organic solvents; these extracts were subsequently subjected to GC/MS analysis. Our results sh…

chemistry.chemical_classificationPollutionPersistent organic pollutantGeologic Sedimentsmedia_common.quotation_subjectExtraction (chemistry)Solid Phase ExtractionSedimentFraction (chemistry)PAHsChemical speciationHumicSandy and muddy sedimentsAquatic ScienceChemical FractionationOceanographyPollutionSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliGas Chromatography-Mass SpectrometrySpeciationHydrocarbonchemistryEnvironmental chemistryOrganic matterPolycyclic Aromatic HydrocarbonsHumic Substancesmedia_commonEnvironmental MonitoringMarine pollution bulletin
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Basis for the Preparative Fractionation of a Statistical Copolymer (SAN) with Respect to Either Chain Length or Chemical Composition

2003

The possibilities to fractionate copolymers with respect to their chemical composition on a preparative scale by means of the establishment of liquid/liquid phase equilibria were studied for random copolymers of styrene and acrylonitrile (SAN). Experiments with solutions of SAN in toluene have shown that fractionation does in this quasi-binary system, where demixing results from marginal solvent quality, take place with respect to the chain length of the polymer only. On the other hand, if phase separation is induced by a second, chemically different polymer, one can find conditions under which fractionation with respect to composition becomes dominant. This opportunity is documented for th…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryFractionationPolymerDimethylacetamideStyreneInorganic ChemistrySolventchemistry.chemical_compoundChemical engineeringMaterials ChemistryCopolymerPolystyreneAcrylonitrileMacromolecules
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Branched versus linear polyisoprene: Fractionation and phase behavior

2007

Abstract Branched polyisoprene (PI) was prepared from PI-macromonomers. Linear byproducts of the synthesized polymer were removed by means of inverse spin fractionation, using the solvent cyclohexane (CH) and the precipitant acetone (AC). A well-defined fraction (Mw = 17.5 kg/mol, Mw/Mn = 1.8) of the branched polyisoprene obtained in this manner was used to determine different phase diagrams with branched and/or linear PI in the mixed solvent CH/AC at 25 °C. For comparable molar masses of the polymers the two-phase area is smallest for the branched PI and slightly larger for the linear PI; in the case of the unfractionated original sample of the branched polymer one observes a pronounced pe…

chemistry.chemical_classificationTernary numeral systemMolar massPolymers and PlasticsCyclohexaneChemistryOrganic ChemistryAnalytical chemistryGeneral Physics and AstronomyPolymer architectureFractionationPolymerchemistry.chemical_compoundPhase (matter)Polymer chemistryMaterials ChemistryPolymer fractionationEuropean Polymer Journal
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Selenium Partitioning and Stable Isotope Ratios in Urban Topsoils

2011

oxides. Th e δ82/76 Se values of total Se in the topsoils were close to the bulk Earth composition with an average δ82/76 Se value of −0.03 ± SD 0.38‰ suggesting that there was no or little Se isotope fractionation in soil. We attribute the small isotope fractionation to the low bioavailability of Se as a consequence of the presence of Fe oxides (adsorbing the dominating Se(IV) forms strongly), organic matter, and SO 4 2− (prevents biouptake of the Se(IV) forms) in the study soils. Small Se isotope fractionations of −0.59 to −0.35‰ in mainly forest soils and of 0.26 to 0.45‰ in mainly alluvial soils were presumably caused by soil/plant-recycling and Se contamination by river water, respecti…

chemistry.chemical_classificationTopsoilIsotopeStable isotope ratioSoil Sciencechemistry.chemical_elementSoil scienceFractionationIsotope fractionationchemistryEnvironmental chemistrySoil waterOrganic matterSeleniumSoil Science Society of America Journal
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Holothuria tubulosa Gmelin 1791 (Holothuroidea, Echinodermata) enhances organic matter recycling in Posidonia oceanica meadows

2014

Abstract The role of Holothuria tubulosa in organic matter recycling of Posidonia oceanica detritus was estimated in a laboratory feeding experiment. The individual mean ingestion rate of seagrass detritus by holothurians was evaluated and carbon and nitrogen stable isotopes, carbon and nitrogen content and C:N ratio analyzed in H. tubulosa , P. oceanica detritus and surface sediment. Results showed that H. tubulosa is capable of ingesting from 30% to 100% of the detritus produced by P. oceanica meadows, depending on the holothurian density. Stable isotope analysis provided evidence for the assimilation of seagrass detritus by H. tubulosa as their signatures were compatible with 1 trophic l…

chemistry.chemical_classificationTotal organic carbonSettore BIO/07 - EcologiabiologyHolothuria tubulosaAquatic Sciencebiology.organism_classificationSea cucumberSeagrasschemistryBenthic zonePosidonia oceanicaBotanyOrganic matterCarbon Ingestion rate Isotopic fractionation Nitrogen Seagrass detritus Sea cucumberEcology Evolution Behavior and SystematicsIsotope analysis
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Fractionation

2012

The enormous diversity of polymers with respect to molecular weight, molecular architecture, and – in the case of copolymers – also the content and arrangement of dissimilar monomers requires well-targeted methods for the separation of the different species that are contained in a given sample. This chapter presents the most abundant fractionation procedures, which are either based on thermodynamic driving forces (like in the case of liquid–liquid phase separation) or on kinetic effects (as with field-flow fractionation).

chemistry.chemical_classificationchemistry.chemical_compoundMonomerChemical engineeringChemistryCopolymerPolymerFractionation
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Tracing the source of gypsum in New Caledonian soils by REE contents and SSr isotopic compositions

1998

Gypsum minerals forming in pedogenic environments in New Caledonia were examined for their S and Sr isotope compositions and REE distributions. Three possible sources were identified: volcanic, soil-derived and marine. However, differentiation based only on the REE contents and normalized patterns was not possible, but, the best preserved volcanic sample yields a negative EuEu∗ anomaly and the lowest GdNYbN ratio due to the high content of organic matter. Mixing calculations of the δ34S values and 87Sr86Sr ratios confirmed that the marine gypsum has a δ34S value close to + 21‰ and an 87Sr86Sr ratio close to 0.70912, and that the volcanic gypsum has a δ34S value of 0‰ and an 87Sr86Sr ratio o…

chemistry.chemical_classificationgeographyGypsumgeography.geographical_feature_categoryGeochemistryMineralogyGeologyFractionationengineering.materialδ34SPedogenesischemistryVolcanoSource rockGeochemistry and PetrologySoil waterengineeringOrganic matterGeologyChemical Geology
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2009

Abstract. Understanding the importance of the different oxidation pathways of sulfur dioxide (SO2) to sulfate is crucial for an interpretation of the climate effects of sulfate aerosols. Sulfur isotope analysis of atmospheric aerosol is a well established tool for identifying sources of sulfur in the atmosphere and assessment of anthropogenic influence. The power of this tool is enhanced by a new ion microprobe technique that permits isotope analysis of individual aerosol particles as small as 0.5 μm diameter. With this new single particle technique, different types of primary and secondary sulfates are first identified based on their chemical composition, and then their individual isotopic…

chemistry.chemical_compoundAmmonium sulfateIsotope fractionationchemistryEnvironmental chemistrySodium sulfateKinetic fractionationchemistry.chemical_elementSulfateSea salt aerosolSulfurEquilibrium fractionationAtmospheric Chemistry and Physics Discussions
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Kristallisation und schmelzverhalten von fraktionen verzweigten polyethylens, 1. Darstellung und charakterisierung der fraktionen

1983

A branched polyethylene with broad molecular weight distribution was separated into a series of fractions by fractional precipitation from dilute solution. The fractions were characterized by viscometric and density measurements, IR-spectroscopy and calorimetry. The methyl group content and the density turned out as largely constant. Molecular weight effects show up in the melting behaviour. The main range of melting and the end of the melting curve shift to lower temperatures with decreasing molecular weight. Compared to the overall extension of the melting range these shifts are small. One has to conclude that polydispersity gives only a minor contribution to the broadening of the melting…

chemistry.chemical_compoundChemistryDispersityPolymer chemistryPartial meltingMolar mass distributionFractionationCalorimetryPolyethyleneMelting curve analysisMethyl groupDie Makromolekulare Chemie
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