Search results for "chemistry [Arsenates]"

showing 10 items of 2372 documents

Microscale magnesium distribution in shell of the Mediterranean mussel Mytilus galloprovincialis: An example of multiple factors controlling Mg/Ca in…

2019

Abstract Since magnesium concentration (Mg/Ca) in biogenic calcite is considered to reflect water temperature during precipitation, the magnesium-to‑calcium ratio has been examined as a proxy for water temperature in paleoclimate research, although factors other than temperature may also influence Mg/Ca in biogenic calcite, thereby introducing a potential bias in the relationship between Mg/Ca and temperature observed in inorganic systems. To better understand factors controlling Mg incorporation into the calcitic shells of bivalves, the distribution of Mg in the Mediterranean mussel Mytilus galloprovincialis was studied, being compared with ambient sea surface temperature (SST), shell grow…

chemistry.chemical_classificationCalciteMediterranean mussel010504 meteorology & atmospheric sciencesbiologyMagnesiumchemistry.chemical_elementGeology010502 geochemistry & geophysicsbiology.organism_classification01 natural sciencesMytiluschemistry.chemical_compoundSea surface temperaturechemistryGeochemistry and PetrologyEnvironmental chemistryOrganic matterGrowth rateMicroscale chemistryGeology0105 earth and related environmental sciencesChemical Geology
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Effects of organic matter complexation on partitioning of transition metals into calcite: Cave-analogue crystal growth experiments

2022

We highlight the potential for first row transition metals to carry paleohydrological signals in speleothems, and argue that these metals constitute valuable proxies for climate reconstructions. Metal availability to speleothems is hypothesised to be restricted by organic complexation, which strongly limits the free ion activity of transition metals (Co2+, Ni2+ and Cu2+) in dripwater, thereby creating a kinetic overprint on metal concentrations and isotope ratios in speleothem calcite. This study presents the results of the first cave-analogue experiments of transition metal partitioning into calcite in the absence and presence of organic ligands. The Geological Microclimate (GeoMic) system…

chemistry.chemical_classificationCalcitegeographyAqueous solutiongeography.geographical_feature_categoryInorganic chemistryNitrilotriacetic acidSpeleothemF800Metalchemistry.chemical_compoundchemistryTransition metalGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumOrganic matterChelation
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Performance of dye-sensitized solar cells based on novel sensitizers bearing asymmetric double D−π−A chains with arylamines as donors

2012

Abstract Three novel, metal-free organic sensitizers bearing two asymmetric double donor-π-acceptor (D-π-A) chains ( DC1 - 3 ), each, and a reference dye containing single D-π-A chain ( SC ) with cyanoacrylic acid as electron acceptor are synthesized. Their photophysical, electrochemical properties and the performances of the corresponding dye-sensitized solar cells (DSSCs) are further investigated. The dyes, DC1, DC2 and DC3 contain one chain with diphenylamine and another chain with carbazole or phenothiazine as electron donor, while diphenylamine is only employed as electron donor in SC . Compared to the inferior solar energy to electricity conversion efficiency ( η ) of 2.82%, 4.66% and…

chemistry.chemical_classificationCarbazoleProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy conversion efficiencyDiphenylamineElectron donorElectron acceptorPhotochemistryElectrochemistrychemistry.chemical_compoundDye-sensitized solar cellchemistryPhenothiazineDyes and Pigments
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Improving lipase activity in solvent-free media by interfacial activation-based molecular bioimprinting

1997

Abstract Nine lipases of mammalian, fungal and bacterial origin and two different model reactions, direct esterification and transesterification (alcoholysis), have been used to probe the potential in solvent-free media of the recently reported strategy of interfacial activation-based molecular (bio)imprinting (IAMI) [Mingarro et al., Proc. Natl. Acad. Sci. USA , 92 (1995) 3308]. The results demonstrate that the imprinting treatment permits nonaqueous rate accelerations which are lipase-dependent and span in some cases up to higher than two orders of magnitude. For several lipases, the method allows conversion yields after short reaction times (in either of the model reactions assayed) whic…

chemistry.chemical_classificationCarboxylic Ester HydrolasesSolvent freebiologyChemistryProcess Chemistry and TechnologyTriacylglycerol lipaseBioengineeringTransesterificationBiochemistryCatalysisInorganic saltsEnzymebiology.proteinOrganic chemistryLipaseJournal of Molecular Catalysis B: Enzymatic
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Stabilization of polynuclear plutonium(IV) species by humic acid

2014

Abstract Although the formation of tetravalent plutonium (Pu(IV)) polymers with natural organic matter was previously observed by spectroscopy, there is no quantitative evidence of such reaction in batch experiments. In the present study, Pu(IV) interaction with humic acid (HA) was investigated at pH 1.8, 2.5 and 3, as a function of HA concentration and for Pu total concentration equal to 6 × 10−8 M. The finally measured Pu(IV) concentrations ([Pu(IV)]eq) are below Pu(IV) solubility limit. Pu(IV)–HA interaction can be explained by the complexation of Pu(IV) monomers by HA up to [Pu(IV)]eq ∼ 10−8 M. However, the slope of the log–log Pu(IV)–HA binding isotherm changes from ∼0.7 to ∼3.5 for hi…

chemistry.chemical_classificationChemistrychemistry.chemical_elementPlutoniumchemistry.chemical_compoundHydrolysisMonomerTetramerGeochemistry and PetrologyHumic acidSolubilitySpectroscopyStoichiometryNuclear chemistryGeochimica et Cosmochimica Acta
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Structurally bound lipids in peat humic acids

2001

Humic acids from highly decomposed peat were subjected to oxidation with alkaline cupric oxide (CuO) at 170°C (single oxidation). Oxidation products were isolated as three fractions, oxidized humic acids, fulvic acids and lipophilic compounds. Isolated oxidized humic acids were subsequently re-oxidized (sequential oxidation) under the same conditions, and released lipophilic compounds were isolated. Lipids released during single and sequential oxidations were determined using capillary gas chromatography and mass spectrometry. Identified compounds accounted for 3.3 and 0.12 wt.% of humic acid content, respectively. Lipid profiles of lipophilic fractions released during single and sequential…

chemistry.chemical_classificationChromatographyOxideFraction (chemistry)Mass spectrometrycomplex mixturesTerpenoidchemistry.chemical_compoundMonomerchemistryGeochemistry and PetrologyOrganic chemistryHumic acidGas chromatographyAbietaneOrganic Geochemistry
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CO2 as a C1-organic building block: Electrocarboxylation of aromatic ketones. A quantitative study of the effect of the concentration of substrate an…

2006

The purpose of this work is to establish and discuss quantitative relationships between the selectivity in preparative scale electrolysis and intrinsic and operational parameters for the electrocarboxylation of aromatic ketones. For the investigated ketones, under appopriate experimental conditions the selectivity of the process is mainly determined by the competition between carboxylation and protonation, de-halogenation reactions (when an halogenated ketone is involved), and possibly dimerizations involving the electrogenerated radical anion. A simple model was proposed to account for these unwanted side paths which allows to predict the dependence of the selectivity as a function of the …

chemistry.chemical_classificationElectrolysisKetoneGeneral Chemical EngineeringInorganic chemistryProtonationSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryElectrocarboxylation Electrochemistry Aromatic ketonesCarbon dioxide Concentration profileAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistryCarboxylationlawElectrochemistryBenzophenoneOrganic chemistrySelectivityAcetophenoneJournal of Electroanalytical Chemistry
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2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides: Synthesis, characterization and ethylene oligomerization

2017

Abstract 2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides (Ni1–Ni8) were synthesized from the respective ligands L1–L8 and characterized. Upon activation with either methylaluminoxane (MAO) or ethylaluminium sesquichloride (EASC), they show high catalytic activity of up to 10.84 × 106 g(oligomer) mol− 1(Ni) h− 1 in ethylene oligomerization. The products range from butenes to dodecenes for Ni1–Ni4, but are limited to butenes and hexenes in the case of Ni5–Ni8. DFT calculations indicate that the Ni C bond length in the model alkyl complexes depends both on the nature of the substituents at the heterocycles and the kind of the alkyl group, shedding some light on the…

chemistry.chemical_classificationEthylene010405 organic chemistryethylene oligomerizationProcess Chemistry and TechnologyMethylaluminoxaneGeneral ChemistryPolyethylene010402 general chemistry01 natural sciencesOligomerMedicinal chemistryCatalysis0104 chemical sciencesCatalysisBond lengthnickel precatalystchemistry.chemical_compoundchemistrysubstituent influenceEthylaluminium sesquichlorideOrganic chemistry7-Aryliminocyclopenta[b]pyridineAlkylCatalysis Communications
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Synthesis and catalytic studies of Ti-anchored disilanol isobutyl-POSS/alkylaluminum system

2012

Abstract Titanium (IV) precursors anchored to alkyl substituted polyhedral oligomeric silsesquioxane (POSS) disilanol were prepared and characterized. These catalysts formulated as [Ti(O^O)2] and [M(O^O)XCl] are found to be active in polymerization of ethylene at high temperatures in combination with ethylaluminum sesquichloride (Et3Al2Cl3) as co-catalyst. The polyethylene product so obtained is linear, crystalline and displays narrow dispersities. The unique low molecular weight PE formed in this reaction exhibit properties that have potential industrial applications. The effect of various reaction parameters on catalyst performance is described.

chemistry.chemical_classificationEthyleneChemistryProcess Chemistry and Technologychemistry.chemical_elementPolyethyleneCatalysisSilsesquioxaneCatalysischemistry.chemical_compoundPolymerizationEthylene polymerizationPolymer chemistryPhysical and Theoretical ChemistryAlkylTitaniumJournal of Molecular Catalysis A: Chemical
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Synthesis, characterization and catalytic behavior of AlTf/UVM-7 as new green catalysts for the glycols etherification reactions

2010

Abstract Bimodal porous Al–UVM-7 system materials with different Si-to-Al ratios were prepared using the Atrane route. These were converted in strong acid heterogeneous AlTf-based catalysts after the treatment with methanolic solutions of triflic acid. The materials so obtained were used as catalysts for the conversion of ethylene glycol (EG) and propylene glycol (PG) with octanol under solvent-free conditions. The process is selective to short ethoxylated structures resulting in the corresponding monoethers. While the conversion of EG and PG was very high (>94%) irrespective of the support characteristics, 1-octanol was transformed only in low degree (3–35%), and its conversion depends on …

chemistry.chemical_classificationEthyleneProcess Chemistry and TechnologySulfonic acidHeterogeneous catalysisCatalysisCatalysisPropenechemistry.chemical_compoundAtranechemistryOrganic chemistryTriflic acidEthylene glycolApplied Catalysis A: General
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