Search results for "decomposition"

showing 10 items of 766 documents

Zur Ökologie Abwasserbelasteter Altrheine

1977

The backwaters of the Upper Rhine can be divided into two types, namely the Sondernheim type and the Leimersheim type. The first one obtains its water mainly from small tributaries of the Rhine, the latter one by the Rhine itself. Both of them are polluted to nearly the same extent by organic matter. In the Sondernheim type biological decomposition starts intensively. It leads to mass-production of a few animal species in the upper, to less production of a large number of animal species in the lower part of its flow. In the Leimersheim type neither biological decomposition, nor mass-production nor a high species-diversity are to be observed. The possible causes of this difference are under …

chemistry.chemical_classificationHydrologygeographygeography.geographical_feature_categorychemistryTributaryEnvironmental scienceOrganic matterAnimal speciesDecomposition
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Nachweis des di-2-cyanoisopropylperoxides bei der zersetzung von azoisobuttersäuredinitril in gegenwart von sauerstoff

1970

Das Di-2-cyanoisopropylperoxid entsteht in etwa 5-proz. Ausbeute bei der Zersetzung von Azoisobuttersaredinitril unter Sauerstoff in Isobutyronitril als Losungsmittel. Thermisch zerfallt das Peroxid est oberhalb von 120°C mit mesbarer Geschwindigkeit in einer Reaktion erster Ordnung. Die Aktivierungsenergie, in Cumol als Losungsmittel, wurde zu 37,9 kcal · mol−1 bestimmt. Werte fur die Zerfallskonstante bei 140°C sind in Cumol 0,057 h−1, in tert-Butylbenzol 0,073 h−1, in Chlorbenzol 0,18 h−1 und in o-Dichlorbenzol 0,23 h−1. Di-2-cyanoisopropylperoxide is formed when azobisisobutyronitrile is decomposed under oxygen in isobutyronitrile as a solvent. The yield amounts to ca. 5%. Thermal decom…

CumeneSolventchemistry.chemical_compoundReaction rate constantchemistryChlorobenzenePolymer chemistryThermal decompositionAzobisisobutyronitrilePeroxideChemical decompositionDie Makromolekulare Chemie
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Optimizing the Binding Energy of the Surfactant to Iron Oxide Yields Truly Monodisperse Nanoparticles.

2018

Despite the great progress in the synthesis of iron oxide nanoparticles (NPs) using a thermal decomposition method, the production of NPs with low polydispersity index is still challenging. In a thermal decomposition synthesis, oleic acid (OAC) and oleylamine (OAM) are used as surfactants. The surfactants bind to the growth species, thereby controlling the reaction kinetics and hence playing a critical role in the final size and size distribution of the NPs. Finding an optimum molar ratio between the surfactants oleic OAC/OAM is therefore crucial. A systematic experimental and theoretical study, however, on the role of the surfactant ratio is still missing. Here, we present a detailed exper…

Thermal decompositionDispersityIron oxideNanoparticle02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundOleic acidPulmonary surfactantchemistryChemical engineeringOleylamineElectrochemistryGeneral Materials Science0210 nano-technologySpectroscopyIron oxide nanoparticlesLangmuir : the ACS journal of surfaces and colloids
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Degradation half-life times of PCDDs, PCDFs and PCBs for environmental fate modeling.

2000

Literature search of the knowledge on the degradation of persistent organic pollutants (POPs) in environmental compartments air, water, soil and sediment was done in purpose to find properties of POPs of interest for modeling. One degradation process, hydrolysis (chemical degradation), was omitted as negligibly slow for POPs studied. The other two, photolysis and biodegradation processes, were considered separately in purpose to develop estimation procedures. The estimates can be given as pseudo first-order rate constants kP for photolysis and kB for biodegradation. For each compartment, an overall degradation rate is k(tot) = kP + kB and lifetime t(1/2) = ln 2/k(tot). The latter values, li…

Environmental EngineeringPolychlorinated DibenzodioxinsPolymersHealth Toxicology and MutagenesisEnvironmental ChemistryWater pollutionChemical decompositionBenzofuransPollutantPersistent organic pollutantPhotolysisChemistryPublic Health Environmental and Occupational HealthSedimentGeneral MedicineGeneral ChemistryBiodegradationPollutionSoil contaminationPolychlorinated BiphenylsKineticsBiodegradation EnvironmentalEnvironmental chemistryDegradation (geology)Environmental PollutantsHalf-LifeChemosphere
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1984

Provided a polymer is soluble, i. e., molecularly dispersed in another polymer irrespective of the molecular weight of the components, the solution is exothermic. By increasing the temperature two effects, both unfavourable to mixing become larger: (i) the excess entropy of mixing caused by contact interaction and (ii) the total effect from the difference of the free volumes of the pure components. So, an upper miscibility gap occurs. The thermodynamic properties of the mixture cannot be derived from the properties of the pure components. They can be described by the corresponding states theory of Prigogine, Flory, and Patterson with suitable values for the contact energy and contact entrop…

chemistry.chemical_classificationExothermic reactionPolyvinyl chloridechemistry.chemical_compoundchemistrySpinodal decompositionPolymer chemistryPolymer blendPolymerEntropy of mixingNeutron scatteringMiscibilityDie Makromolekulare Chemie
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Decarboxylation and alkaline colour fading reactions in presence of humic substances.

2002

Humic substances (HSs) can substantially influence velocity of reactions in the environment as shown on example of decarboxylation and alkaline colour (e.g., malachite green and crystal violet) fading reactions. In colour fading and decarboxylation reactions of 6-nitrobenzisoxazole-3-carboxylic acid HS act as inhibitors, but additions of surfactants change the pattern of reaction. The inhibitory activity of HSs much depends on their origin. The velocity of studied reactions depends also on pH, temperature and concentration of HS used. Possible micellar catalysis mechanism has been suggested.

Models MolecularReaction mechanismEnvironmental Engineeringgenetic structuresDecarboxylationHealth Toxicology and MutagenesisInorganic chemistryCarboxylic AcidsColorDecarboxylationCatalysisCatalysischemistry.chemical_compoundSurface-Active AgentsHydroxidesRosaniline DyesEnvironmental ChemistryHumic acidCrystal violetMalachite greenChemical decompositionHumic SubstancesMicelleschemistry.chemical_classificationPublic Health Environmental and Occupational HealthTemperatureGeneral MedicineGeneral ChemistryReaction inhibitorHydrogen-Ion ConcentrationPollutionKineticschemistryGentian VioletChemosphere
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Synthesis, Characterization and Magnetic Properties of New Dinuclear Copper(II) Complexes with N,N′-Disubstituted Dithiooxamides derived from α-Amino…

2005

Four new dinuclear copper(II) complexes have been synthesized and have the general formula [Cu2(L)(H2O)2], where L = GLYDTO [N,N′-bis(carboxymethyl)dithiooxamide], ALADTO [N,N′-bis(carboxyethyl)dithiooxamide], VALDTO [N,N′-bis(1-carboxy-2-methylpropyl)dithiooxamide] and LEUDTO [N,N′-bis(1-carboxy-3-methylbutyl)dithiooxamide]. The complexes were characterized by elemental analysis as well as by IR, electronic and EPR spectroscopy. These techniques provided evidence for the presence of the CuNO2S chromophore. Magnetic susceptibility measurements on all the complexes in the range 4–300 K show the existence of a dominant antiferromagnetic interaction with −J values greater than 300 cm−1. Therma…

Inorganic chemistryThermal decompositionchemistry.chemical_elementChromophoreMagnetic susceptibilityCopperlaw.inventionInorganic ChemistryThermogravimetryCrystallographychemistry.chemical_compoundDithiooxamidechemistrylawAntiferromagnetismElectron paramagnetic resonanceZeitschrift für anorganische und allgemeine Chemie
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Volatile compounds extracted from polypropylene pellets by hot water: influence of the level of the peroxide agents

1992

To improve the quality level of plastic packaging materials, we determined the influence of chemical degradation of polypropylene (PP) upon the amount of volatile components extracted by hot water from PP pellets. Two formulations were analyzed and compared: PP CR (degraded) and PP (not degraded). After Likens-Nickerson's extraction of the pellets and concentration of the extract, an HPLC fractionation was made to collect three fractions of different poiarities: a pentane (A), a dichloromethane (B), and an ether (C) fraction. Fractions (B) and (C) were olfactively evaluated by GC sniffing to be most interesting. Their analysis by GC/MS coupling allowed the identification of different compon…

ChromatographyPolymers and PlasticsNonanal[SDV]Life Sciences [q-bio]010401 analytical chemistryPellets02 engineering and technologyGeneral ChemistryDecanal021001 nanoscience & nanotechnology01 natural sciencesPeroxide0104 chemical sciencesSurfaces Coatings and FilmsPentane[SDV] Life Sciences [q-bio]chemistry.chemical_compoundchemistryMaterials ChemistryPhenols0210 nano-technologyChemical decompositionComputingMilieux_MISCELLANEOUSDichloromethane
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Multi-subject fMRI analysis via combined independent component analysis and shift-invariant canonical polyadic decomposition

2014

Canonical polyadic decomposition (CPD) may face a local optimal problem when analyzing multi-subject fMRI data with inter-subject variability. Beckmann and Smith proposed a tensor PICA approach that incorporated an independence constraint to the spatial modality by combining CPD with ICA, and alleviated the problem of inter-subject spatial map (SM) variability.This study extends tensor PICA to incorporate additional inter-subject time course (TC) variability and to connect CPD and ICA in a new way. Assuming multiple subjects share common TCs but with different time delays, we accommodate subject-dependent TC delays into the CP model based on the idea of shift-invariant CP (SCP). We use ICA …

Independent component analysis (ICA)Speech recognitionModels NeurologicalMotor ActivityNeuropsychological TestsInter-subject variabilityta3112TimeMulti-subject fMRI dataFingersHumansCanonical polyadic decomposition (CPD)Computer SimulationMotor activityInvariant (mathematics)ta217ta113Brain MappingShift-invariant CP (SCP)General NeuroscienceBrainMagnetic Resonance ImagingIndependent component analysisAuditory PerceptionTensor PICASpatial mapsPsychologyAlgorithmJournal of Neuroscience Methods
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Application of the Structural Decomposition Analysis to assess the indirect energy consumption and air emission changes related to Italian households…

2012

Abstract The design of sustainable production and consumption strategies and the assessment of implemented actions require to identify the driving forces that influence the trend of energy consumption and environmental impacts. For this purpose, the Structural Decomposition Analysis (SDA) was developed as a suitable methodology to analyse the driving forces of the changes in economic, energy and environmental indicators. The paper presents one of the first Italian studies that apply an energy and environmental extended input–output model, opportunely shaped to the examined context, combined with SDA. In detail, it aims at: (1) investigating the energy use and the air emissions arisen from t…

Consumption (economics)Settore ING-IND/11 - Fisica Tecnica AmbientaleRenewable Energy Sustainability and the EnvironmentInput–output modelEconomic sectorEnvironmental engineeringContext (language use)Energy consumptionEnvironmental economicsEmission intensityEnergy accountinginput-output analysis Structural decomposition analysis energy consumption Air emissionsEconomicsProduction (economics)Renewable and Sustainable Energy Reviews
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