Search results for "Phosphor"

showing 10 items of 1952 documents

Design of nutrient removal activated sludge systems

2003

A mechanistic mathematical model for nutrient and organic matter removal was used to describe the behavior of a nitrification denitrification enhanced biological phosphorus removal (NDEBPR) system. This model was implemented in a user-friendly software DESASS (design and simulation of activated sludge systems). A 484-L pilot plant was operated to verify the model results. The pilot plant was operated for three years over three different sludge ages. The validity of the model was confirmed with data from the pilot plant. Also, the utility of DESASS as a valuable tool for designing NDEBPR systems was confirmed.

chemistry.chemical_classificationEnvironmental EngineeringDenitrificationActivated sludgeNutrientEnhanced biological phosphorus removalPilot plantchemistryEnvironmental scienceOrganic matterNitrificationPulp and paper industryWater Science and TechnologyWater Science and Technology
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Significance of Posttranslational Modification of Drug Metabolizing Enzymes by Phosphorylation for the Control of Carcinogenic Metabolites

1995

The total activity of foreign compound metabolizing enzymes may change by altering the amount or the specific activity of the enzyme by induction or repression, or by activation or inhibition. The important contribution of enzyme induction is well known (Conney 1982, Oesch 1986, Nebert and Jones 1989). This is a relatively slow process which requires the biosynthesis of the enzyme protein. The possibility of a faster regulation of foreign compound metabolism by posttranslational modification by phosphorylation of an already preexisting protein molecule has only recently received attention. A central role in the metabolism of foreign compounds is played by the cytochrome P450-dependent monoo…

chemistry.chemical_classificationEnzymechemistryCytochromebiologyBiochemistrySecond messenger systembiology.proteinCytochrome P450PhosphorylationMetabolismMonooxygenaseEnzyme inducer
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Synthesis of low density poly(ethylene) using nickel iminophosphonamide complexes

2007

Ethylene polymerization using a catalyst derived from the reaction of the phosphorane (Me3Si)2NP(NSiMe3)2 (1) with either Ni(COD)2 or bis(π-allyl)Ni complexes affords branched poly(ethylene) (PE) of variable MW (103−106) depending on conditions. The branched PE of high MW is semicrystalline with Tm < 100 °C. High field 13C NMR spectra reveal the presence of methyl branches (ca. 10−15 per 1000 C atoms), branches longer than six C atoms (15−20 per 1000 C atoms) and trace levels of ethyl, propyl, n-butyl, and sec-butyl branches (total <2 per 1000 C atoms). The branching distribution changes modestly in response to changes in ethylene pressure in a manner consistent with a chain-walking mechani…

chemistry.chemical_classificationEthylenePolymers and PlasticsStereochemistryOrganic ChemistryPolymerCarbon-13 NMRBranching (polymer chemistry)PhosphoraneInorganic Chemistrychemistry.chemical_compoundCrystallographyCrystallinitychemistryPolymerizationMaterials ChemistryMoleculeMacromolecules
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Fast proton conduction in hydrogen bonded microheterogeneous systems: Bis(2-ethylhexyl)phosphoric acid/N-methyl formamide liquid mixtures

2009

Structural and dynamical properties of bis(2-ethylhexyl)phosphoric acid (HDEHP)/N-methyl formamide (NMF) liquid mixtures in the whole composition range have been investigated by Fourier Transform Infrared spectroscopy (FT-IR), X-rays Diffraction (XRD), and AC complex impedance spectroscopy. Driven by hydrogen bond interactions among HDEHP PO(4)H group and NMF CO and NH groups, and also by steric effects among the HDEHP alkyl chains, the system microstructure is mainly characterized by the coexistence of spatially separated hydrophilic and hydrophobic nanodomains showing local organization and short-range order. The evolution of this structural feature with system composition has been highli…

chemistry.chemical_classificationFormamideHydrogen bondAnalytical chemistryInfrared spectroscopyFast proton conduction systems Microheterogeneous liquid mixtures Bis(2-ethylhexyl)phosphoric acid N-methyl formamidePercolation thresholdSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryX-ray crystallographyFourier transform infrared spectroscopyPhosphoric acidAlkylSettore CHIM/02 - Chimica FisicaJournal of Colloid and Interface Science
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An Au(iii)–amino alcohol complex for degradation of organophosphorus pesticides

2015

An Au(III)–amino alcohol complex has been used to cleave organophosphorous pesticides of the dithiophosphate family. P–S bond breaking was readily demonstrated by 1H NMR, 31P NMR and MS. Thiol fragment release was also demonstrated using 2,4-dinitrobenzenesulfonyl fluorescein ethyl ester as a fluorescent sensor.

chemistry.chemical_classificationGeneral Chemical EngineeringAlcoholGeneral ChemistryFluorescenceMedicinal chemistrychemistry.chemical_compoundchemistryCleaveThiolProton NMROrganic chemistryDegradation (geology)FluoresceinOrganophosphorus pesticidesRSC Advances
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Regulatory features of glycogen phosphorylase from frog brain (Rana temporaria)

1985

1. Glycogen content and the activity of glycogen phosphorylase (GPase) are much higher in brain tissue of the Common frog (Rana temporaria) than in brain tissue of mammals and birds (Table 1). 2. In phosphate buffer GPase is extracted from frog orain in a form completely active without addition of AMP and has therefore to be regarded as phosphorylase a. Several procedures to extract the b-form of the enzyme from the tissue have been unsuccessful. In resting skeletal muscle predominantly the AMP dependent b-form is present (Table 1). 3. In vitro, however, the existence of the complete interconverting system can be demonstrated. If NaF (a phosphatase inhibitor) was omitted from the homogeniza…

chemistry.chemical_classificationGlycogenPhysiologySkeletal muscleMetabolismBiologyBiochemistryGlycogen phosphorylasechemistry.chemical_compoundEndocrinologymedicine.anatomical_structureEnzymechemistryBiochemistrymedicineGRENOUILLEAnimal Science and ZoologyProtein phosphorylationEcology Evolution Behavior and SystematicsHomogenization (biology)Journal of Comparative Physiology B
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Calcium effect on enhanced biological phosphorus removal.

2006

The role of calcium (Ca) in enhanced biological phosphorus removal and its possible implications on the metabolic pathway have been studied. The experience has been carried out in an SBR under anaerobic–aerobic conditions for biological phosphorus removal during 8 months. The variations of influent Ca concentration showed a clear influence on the EBPR process, detecting significant changes in YPO4. These YPO4 variations were not due to influent P/COD ratio, pH, denitrification and calcium phosphate formation. The YPO4 has been found to be highly dependent on the Ca concentration, increasing as Ca concentration decreases. The results suggest that high Ca concentrations produce “inert” granul…

chemistry.chemical_classificationHigh concentrationEnvironmental EngineeringDenitrificationSewagePolyphosphateInorganic chemistrychemistry.chemical_elementPhosphorusMetabolismCalciumAerobiosisWater PurificationMetabolic pathwaychemistry.chemical_compoundEnhanced biological phosphorus removalBioreactorschemistryEnvironmental chemistryCalciumAnaerobiosisCounterionWater Pollutants ChemicalWater Science and TechnologyWater science and technology : a journal of the International Association on Water Pollution Research
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Decoupling of Dynamic Processes in Surfactant-Based Liquid Mixtures: The Case of Lithium-Containing Bis(2- ethylhexyl)phosphoric Acid/Bis(2-ethylhexy…

2014

Pure surfactant liquids and their binary mixtures, because of the amphiphilic nature of the molecules involved, can exhibit nanosegregation and peculiar transport properties. The idea that inspired this work is that the possibility of including in such media salts currently used for technological applications should lead to a synergy between the properties of the salt and those of the medium. Therefore, the dynamic features of bis(2-ethylhexyl)amine (BEEA) and bis(2-ethylhexyl)phosphoric acid (HDEHP) liquid mixtures were investigated as a function of composition and temperature by (1)H nuclear magnetic resonance (NMR) spectroscopy and rheometry. Inclusion of litium trifluoromethanesulfonate…

chemistry.chemical_classificationInorganic chemistryInfrared spectroscopychemistry.chemical_elementSalt (chemistry)Lithium-Containing Bis(2-ethylhexyl)phosphoric Acid/Bis(2-ethylhexyl)amine SystemsSurfaces and InterfacesCondensed Matter Physicschemistry.chemical_compoundsurfactant-based liquid mixtures physico chemical propertieschemistryPulmonary surfactantElectrochemistryGeneral Materials ScienceAmine gas treatingLithiumPulsed field gradientTrifluoromethanesulfonatePhosphoric acidSpectroscopySettore CHIM/02 - Chimica Fisica
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Oxidative halogenation of substituted pyrroles with Cu(II). PartIII. Bromination and chlorination of 2-benzoylpyrrole

1992

The bromination of 2-benzoylpyrrole with copper(II) bromide in the homogeneous and the heterogeneous phase is described, giving 4- and 5-monobromo derivatives whose ratio decreases as the temperature is increased. The same reaction with copper(II) chloride in acetonitrile at 60° produces 5-chloro-2-benzoylpyrrole as the major product. 4,5-Dihalopyrroles in good yields are obtained with an excess of halogenating agent.

chemistry.chemical_classificationKetoneChemistryOrganic ChemistryHalogenationchemistry.chemical_elementOxidative phosphorylationMedicinal chemistryChlorideCopperchemistry.chemical_compoundBromidePhase (matter)medicineOrganic chemistryAcetonitrilemedicine.drugJournal of Heterocyclic Chemistry
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Red-light-emitting electrochemical cell using a polypyridyl iridium(III) polymer.

2009

A deep-red phosphorescent ionic iridium(III) complex is prepared and incorporated into a polymer. Both the complex (1) and the polymer (2) were used as the single active material in solid-state light-emitting electrochemical cells (LECs). The devices built up using 1 and 2 emit in the deep-red region of the visible spectrum with CIE coordinates x = 0.710; y = 0.283 and x = 0.691; y = 0.289, respectively, making them one of the deepest-red emitting LECs reported. It is the first example of a polymeric LEC incorporating an ionic iridium complex, which exhibits increased stabilities compared with the device based on the small molecular weight complex.

chemistry.chemical_classificationMaterials scienceLuminescent MeasurementsLightPolymersIonic bondingchemistry.chemical_elementPolymerElectrochemical TechniquesPhotochemistryIridiumElectrochemical cellInorganic ChemistrychemistryCoordination ComplexesLuminescent MeasurementsIridiumRed lightPhosphorescenceVisible spectrumDalton transactions (Cambridge, England : 2003)
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