Search results for "CARBONATE"

showing 10 items of 920 documents

Common genetic denominators for Ca++-based skeleton in Metazoa: role of osteoclast-stimulating factor and of carbonic anhydrase in a calcareous spong…

2012

Calcium-based matrices serve predominantly as inorganic, hard skeletal systems in Metazoa from calcareous sponges [phylum Porifera; class Calcarea] to proto- and deuterostomian multicellular animals. The calcareous sponges form their skeletal elements, the spicules, from amorphous calcium carbonate (ACC). Treatment of spicules from Sycon raphanus with sodium hypochlorite (NaOCl) results in the disintegration of the ACC in those skeletal elements. Until now a distinct protein/enzyme involved in ACC metabolism could not been identified in those animals. We applied the technique of phage display combinatorial libraries to identify oligopeptides that bind to NaOCl-treated spicules: those oligop…

Anatomy and PhysiologyMarine and Aquatic Scienceslcsh:MedicineBiochemistryCalcium Chloridechemistry.chemical_compoundMolecular Cell BiologySycon raphanuslcsh:ScienceCarbonic AnhydrasesSclerocytechemistry.chemical_classification0303 health sciencesMultidisciplinaryCalcareous spongebiology030302 biochemistry & molecular biologyIntracellular Signaling Peptides and ProteinsRecombinant ProteinsAmorphous calcium carbonatePoriferaEnzymesChemistrymedicine.anatomical_structureBiochemistryMedicineOligopeptidesResearch ArticleBiotechnologyDNA ComplementaryMolecular Sequence DataMarine BiologyCalcium Carbonate03 medical and health sciencesSponge spiculeOsteoclastCarbonic anhydraseChemical BiologymedicineAnimalsAmino Acid SequenceBiology030304 developmental biologySequence Homology Amino AcidEvolutionary Developmental Biologylcsh:Rbiology.organism_classificationEnzymechemistryEarth Sciencesbiology.proteinCalciumlcsh:QPeptidesPhysiological ProcessesDevelopmental BiologyPLoS ONE
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Natural Compounds as Sustainable Additives for Biopolymers

2020

In the last few decades, the interest towards natural compounds, coming from a natural source and biodegradable, for biopolymers is always increasing because of a public request for the formulation of safe, eco-friendly, and sustainable materials. The main classes of natural compounds for biopolymers are: (i) naturally occurring fillers (nFil), such as nano-/micro- sized layered alumino-silicate: halloysite, bentonite, montmorillonite, hydroxyapatite, calcium carbonate, etc.; (ii) naturally occurring fibers (nFib), such as wood and vegetable fibers; (iii) naturally occurring antioxidant molecules (nAO), such as phenols, polyphenols, vitamins, and carotenoids. However, in this short review, …

AntioxidantPolymers and Plasticsmedicine.medical_treatmentbiopolymersReviewengineering.materialHalloysiteNatural (archaeology)lcsh:QD241-441chemistry.chemical_compoundnatural fiberslcsh:Organic chemistrybiopolymermedicineOrganic chemistryPhenolsnatural antioxidantsnatural fillerSettore CHIM/06 - Chimica OrganicaGeneral Chemistrynatural fibernatural fillersSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiMontmorilloniteCalcium carbonatechemistryPolyphenolBentoniteengineeringPolymers
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Orbital chronology of the lower-middle Aptian: palaeoenvironmental implications (Serre Chaitieu section, Vocontian Basin).

2013

4 pages; International audience; A detailed cyclostratigraphic study conducted on several proxies including spectral gamma ray, magnetic susceptibility, clay minerals, and carbonate content suggests that the return to equilibrium in the carbon cycle after the major disturbance linked with Oceanic Anoxic Event 1a occurred in about 2 Myr. The minimum duration of the D. furcata zone is estimated at 0.46 Myr and that of the E. subnodosocostatum zone at 1.45 Myr. Strengthening of the obliquity record in the furcata zone confirms the cooling that characterizes this period.

AptianCyclostratigraphySerre ChaitieuStructural basin010502 geochemistry & geophysics[ SDU.STU.ST ] Sciences of the Universe [physics]/Earth Sciences/Stratigraphy01 natural sciencesCarbon cyclePaleontologychemistry.chemical_compoundstomatognathic system0103 physical sciencesAptian010303 astronomy & astrophysics0105 earth and related environmental sciencesOceanic Anoxic Event 1amyrCyclostratigraphyVocontian Basinchemistry13. Climate action[SDU.STU.ST]Sciences of the Universe [physics]/Earth Sciences/StratigraphyPeriod (geology)CarbonateGeologyChronology
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( n ‐Bu 2 Sn) 2 O(CO 3 ): An active, robust and recyclable organotin(IV) for the direct synthesis of linear organic carbonates from carbon dioxide an…

2017

Organotin(IV) compounds are known to promote the direct synthesis of organic carbonates from carbon dioxide and alcohols. In the past, structural studies have highlighted that the carbonato moiety is a recurring ligand of tin species collected during CO2 pressurized reactions. In a mimetic approach and in order to achieve an available and recyclable precursor, the title compound (n-Bu2Sn)2O(CO3) (1) was prepared in a single step by reacting commercial di-n-butyltin dichloride with an aqueous solution of sodium carbonate. Compound 1 was characterized using infrared spectroscopy and thermogravimetric and elemental analyses. Multinuclear NMR investigations in solution were also conducted. Comp…

Aqueous solution010405 organic chemistryChemistryCarbonationInfrared spectroscopychemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundOrganic chemistryMoietyMethanolDimethyl carbonateSodium carbonateTinApplied Organometallic Chemistry
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Ferromagnetic coupling through a carbonate bridge in the copper (II) chain [Cu(CO3)(4-apy)2] · H2O (4-apy = 4-aminopyridine)

1999

Abstract Atmospheric CO2 fixation by aqueous solutions containing copper(II) bromide and 4-aminopyridine (4-apy) yields the first carbonatobridged copper(II) chain of formula [Cu(CO3)(4-apy)2] · H2O that exhibits an intrachain ferromagnetic coupling.

Aqueous solutionInorganic chemistrychemistry.chemical_elementCrystal structureCopperInorganic ChemistryCoupling (electronics)Crystallographychemistry.chemical_compoundchemistryFerromagnetismBromideMaterials ChemistryCarbonateCupratePhysical and Theoretical ChemistryInorganic Chemistry Communications
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Electrochemical reduction of graphene oxide films in aqueous and organic solutions

2013

Abstract Electrochemical reduction of graphene oxide (GO) films cast on tin oxide glass substrates were carried out in aqueous solutions and in propylene carbonate and acetonitrile. Cyclic voltammetric measurements indicate successful reduction of GO films. The reduction process begins in aqueous solutions at less negative potentials than in organic solutions. Additionally the pH value of the aqueous solutions influences the reduction potential. According to spectroscopic analysis the reduction process of the GO film can be controlled by the choice of reduction potential and electrolyte medium. The potential window in this work was made broader by increasing pH or by using organic electroly…

Aqueous solutionMaterials scienceGrapheneGeneral Chemical EngineeringInorganic chemistryOxideElectrolyteElectrochemistryTin oxidelaw.inventionchemistry.chemical_compoundchemistrylawPropylene carbonateElectrochemistryAcetonitrileta116Electrochimica Acta
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Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Aqueous solutionProtonation of carbonateSpecific ion interaction theory (SIT)Ion pair formation modelChemistryInorganic chemistryTetraalkylammonium saltProtonationDependence on ionic strengthElectrolyteIon pairsAnalytical Chemistrychemistry.chemical_compoundIonic strengthTetramethylammonium chlorideAqueous solutionPitzer equationsCarbonateSettore CHIM/01 - Chimica AnaliticaProtonation of carbonate; Dependence on ionic strength; Aqueous solution; Tetraalkylammonium salts; Ion pair formation model; Specific ion interaction theory (SIT); Pitzer equationPitzer equation
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Antivirale Wirkstoffe, 20. Mitt. 4,6-Dialkylierte 2-Benzylthiopyrimidine

1981

Aus der Kondensation von Benzylisothioharnstoff (1) mit den β-Diketonen 2a–c gehen die 2-Benzylthiopyrimidine 3a–c hervor. Wird die Reaktion 1+2b jedoch in 30proz. wasr. Kaliumcarbonat-Losung/Ethanol/Ether durchgefuhrt, so tritt unter Ethanolyse Bildung von 2-Ethoxy-4,6-diethylpyrimidin (4) ein. 2-Benzylthio-4-ethyl-6-(trifluormethyl)pyrimidin ubt Hemmwirkung gegen Influenza A-Virus aus. Antiviral Agents, XX: 4,6-Dialkylated 2-Benzylthiopyrimidines Condensations of benzylisothiourea (1) with the β-diketones 2a–c yield the 4,6-dialkylated 2-benzylthiopyrimidines 3a–c. However, in 30% aqueous potassium carbonate solution/ethanol/ether, the reaction 1+2b proceeds by ethanolysis to form 2-ethox…

Aqueous solutionTrifluoromethylEthanolPyrimidineStereochemistryPharmaceutical ScienceEthermedicine.disease_causePotassium carbonatechemistry.chemical_compoundchemistryDrug DiscoveryInfluenza A virusmedicineArchiv der Pharmazie
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Jurassic evolution of the Arabian carbonate platform edge in the central Oman Mountains

2005

International audience; The Jurassic Sahtan Group exposed in northern Oman was deposited in shallow marine environments at the edge of the Arabian Platform facing the Neo-Tethys (Hamrat Duru Basin). The upper Sahtan Group is made up of a mixed siliciclastic-carbonate unit overlain by pure carbonate deposits, assigned to a Bathonian and Early Callovian age on the basis of brachiopods and foraminifers. These carbonate depositional systems were composed of outer oolitic shoals that underwent subaerial exposure, and a deeper, somewhat restricted, gently dipping shelf interior. Oolitic material was shed off the platform edge into the deep-sea depositional complex of the Guweyza Formation. The Sa…

Arabian-PeninsulaCarbonate platformJurassic[ SDU.STU.ST ] Sciences of the Universe [physics]/Earth Sciences/Stratigraphy010502 geochemistry & geophysics01 natural sciencesUnconformityOnlapSedimentary depositional environmentPaleontologychemistry.chemical_compoundcarbonate platformcarbonate-platform14. Life underwaterTethys010503 geology0105 earth and related environmental sciencesGeologyfacieschemistry[SDU.STU.ST]Sciences of the Universe [physics]/Earth Sciences/StratigraphySubaerial[SDU.STU.ST] Sciences of the Universe [physics]/Earth Sciences/StratigraphyArabian PeninsulaCarbonateSedimentary rockGeologyMarine transgressionJournal of the Geological Society
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Primary Cell Culture of Fresh Water Hyriopsis cumingii Mantle/Pearl Sac Tissues and Its Effect on Calcium Carbonate Mineralization

2014

Primary cell cultures of the fresh water Hyriopsis cumingii mantle and pearl sac tissues were produced in this study, and the influence of the tissue, cells, and secreted protein on calcium carbonate crystal nucleation and growth was studied. The study contributes to a further understanding of the influence of organic matrices on CaCO3 crystal formation. This research started from the protein level to the tissue/cell level, which is crucial for understanding the inorganic deposition process. The new data also add relevant theoretical approaches to an overall understanding of biomineralization processes. In the experimental groups with mantle or pearl sac tissue, the growth patterns of arago…

AragoniteMineralogyCrystal growthGeneral Chemistryengineering.materialCondensed Matter PhysicsMineralization (biology)Amorphous calcium carbonatechemistry.chemical_compoundCalcium carbonatechemistryCell cultureBiophysicsengineeringGeneral Materials ScienceMantle (mollusc)BiomineralizationCrystal Growth & Design
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