Search results for " carbonate"

showing 10 items of 381 documents

Organo-catalyzed synthesis of aliphatic polycarbonates in solvent-free conditions

2012

A new efficient and expeditious route to the synthesis of aliphatic polycarbonates, in solvent-free conditions and using 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) as a catalyst precursor, is described. The protocol consists of a two-step polymerization process involving the transesterification of dimethyl carbonate (DMC) with linear alkane diols and leading to high molecular weight homopolymers. The reaction went to completion quantitatively with the liberation of methanol as the only by-product. The in situ formation of N-heterocyclic carbene species resulting from BMIM-2-CO2 decarboxylation is suggested to be a key feature of the condensation process. The protocol was then …

Alkanechemistry.chemical_classificationPolymers and PlasticsDecarboxylationOrganic ChemistryBioengineeringTransesterificationBiochemistryCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryCopolymerOrganic chemistryMethanolDimethyl carbonatePolymer Chemistry
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Decomposition of ammonium sulfate residue in a high solid/gas ratio suspension state with an industrial-scale reactor system (production line)

2015

Abstract Ammonium sulfate residue is a particulate solid and is produced during the manufacture of ammonium sulfate fertilizer. The residue used in this study contained a large portion of calcium carbonate, from which active lime (CaO) was recovered via thermal decomposition. We used a purpose-built device to decompose the residue in a semi-suspension state. We found that CaO had the highest activity when residue was decomposed at 850–900 °C. Our experiments indicated that ammonium sulfate residue should be decomposed in a suspension state to produce active CaO. Based on our laboratory test findings, an industrial-scale production line with a high solid/gas ratio in a suspension state was d…

Ammonium sulfateGeneral Chemical EngineeringInorganic chemistryThermal decompositionengineering.materialParticulatesDecompositionchemistry.chemical_compoundResidue (chemistry)Calcium carbonatechemistryengineeringGeneral Materials ScienceCitric acidLimeParticuology
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Amorphous, nanocrystalline and crystalline calcium carbonates in biological materials

2010

Raman spectroscopy is a powerful tool in identifying different calcium carbonate polymorphs. Here, the method is applied to cultured pearls from freshwater (genus Hyriopsis) and marine bivalve species (Pinctada maxima) as well as to shells of Diplodon chilensis patagonicus bivalves. Raman spectra for vaterite, detected for the first time in an adult shell, and amorphous calcium carbonate (ACC) are discussed. Results for ACC are compared with those of synthetically produced ACC and with the Raman spectroscopic features of stable biogenic ACC from the crustacean Porcellio scaber. Decomposition of the most intense signal of all calcium carbonate polymorphs—the ν1 symmetric stretching mode of t…

Analytical chemistryMineralogyAmorphous calcium carbonateNanocrystalline materialAmorphous solidchemistry.chemical_compoundCrystallinitysymbols.namesakeCalcium carbonatechemistryVateritesymbolsCarbonateGeneral Materials ScienceRaman spectroscopySpectroscopyJournal of Raman Spectroscopy
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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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( 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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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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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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