Search results for "hydration"

showing 10 items of 217 documents

Proteome analysis of leaves of the desiccation-tolerant grass, Sporobolus stapfianus, in response to dehydration.

2011

Drought and its affects on agricultural production is a serious issue facing global efforts to increase food supplies and ensure food security for the growing world population. Understanding how plants respond to dehydration is an important prerequisite for developing strategies for crop improvement in drought tolerance. This has proved to be a difficult task as all of the current research plant models do not tolerate cellular dehydration well and, like all crops, they succumb to the effects of a relatively small water deficit of -4MPa or less. For these reasons many researchers have started to investigate the usefulness of resurrection plants, plants that can survive extremes of dehydratio…

ProteomeDifference gel electrophoresisDrought tolerancePlant ScienceHorticulturePoaceaeBiochemistryModels BiologicalTwo-Dimensional Difference Gel Electrophoresischemistry.chemical_compoundBotanymedicineBrassinosteroidDehydrationMolecular BiologyPlant ProteinsbiologyDehydrationfungiRuBisCOfood and beveragesGeneral Medicinemedicine.diseasebiology.organism_classificationPlant LeaveschemistryBiochemistryProteomebiology.proteinSporobolusDesiccationSignal TransductionPhytochemistry
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Proton, Hydroxide Ion, and Oxide Ion Affinities of Closed-Shell Oxides: Importance for the Hydration Reaction and Correlation to Electronic Structure

2019

Phenomenologically, the enthalpy of the dissociative water incorporation (hydration) of oxides is often found to be more favorable for more basic oxides. In the present work, we investigate proton,...

ProtonChemistryInorganic chemistryEnthalpy02 engineering and technologyElectronic structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAffinities0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonchemistry.chemical_compoundGeneral EnergyHydration reactionHydroxidePhysical and Theoretical Chemistry0210 nano-technologyOpen shellThe Journal of Physical Chemistry C
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Anharmonic activations in proteins and peptide model systems and their connection with supercooled water thermodynamics

2016

International audience; — Proteins, the nano-machines of living systems, are highly dynamic molecules. The timescale of functionally relevant motions spans over a very broad range, from femtoseconds to several seconds. In particular, the pico-to nanoseconds region is characterized by side-chain and backbone anharmonic fluctuations that are responsible for many biological tasks like ligand binding, substrate recognition and enzymatic activity. Neutron scattering on hydrated protein powders reveals two main activations of anharmonic dynamics, characterized by different onset temperature and amplitude. Here we review our work on synthetic polypeptides, native proteins, and single amino acids t…

Quantitative Biology::Biomolecules[SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry Molecular Biology/Structural Biology [q-bio.BM][SDV]Life Sciences [q-bio][SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyNeutron scatteringProtein dynamicsLiquid-liquid crossoverComputingMilieux_MISCELLANEOUSHydration waterSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)
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Mapping geographical inequalities in oral rehydration therapy coverage in low-income and middle-income countries, 2000-17

2020

Background: Oral rehydration solution (ORS) is a form of oral rehydration therapy (ORT) for diarrhoea that has the potential to drastically reduce child mortality; yet, according to UNICEF estimates, less than half of children younger than 5 years with diarrhoea in low-income and middle-income countries (LMICs) received ORS in 2016. A variety of recommended home fluids (RHF) exist as alternative forms of ORT; however, it is unclear whether RHF prevent child mortality. Previous studies have shown considerable variation between countries in ORS and RHF use, but subnational variation is unknown. This study aims to produce high-resolution geospatial estimates of relative and absolute coverage o…

RJ101medicine.medical_treatmentCHILDRENZINC0302 clinical medicine030212 general & internal medicinemedia_commonGeographylcsh:Public aspects of medicine1. No povertyLow income and middle income countriesGeneral Medicine3142 Public health care science environmental and occupational health3. Good healthPeer reviewGeographyChild PreschoolA990 Medicine and Dentistry not elsewhere classifiedGeographical inequalities0605 MicrobiologyDiarrheaAFRICAInequalityDEATHSmedia_common.quotation_subject030231 tropical medicineDeveloping countryArticleRS1117 Public Health and Health Services03 medical and health sciencesMORBIDITYEnvironmental healthDIARRHEAL DISEASEmedicineHumansOral rehydration therapyHealthcare DisparitiesDeveloping CountriesModels StatisticalCHOLERAMORTALITYInfant NewbornInfantlcsh:RA1-1270Bayes TheoremMiddle incomeGLOBAL BURDENChild mortality0605 Microbiology 1117 Public Health and Health ServicesHealth Care SurveysITC-ISI-JOURNAL-ARTICLEFluid TherapyNAHuman medicineITC-GOLD
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Propan-2-ol dehydration on H-ZSM-5 and H-Y zeolite: a DFT study

2012

The catalytic dehydration of propan-2-ol over H-Y and H-ZMS-5 aluminated zeolite models, mimicking both internal cavities and external surfaces, was studied by DFT calculations to investigate the reaction mechanism. After the adsorption of propan-2-ol on the zeolite, the dehydration mechanism starts with alcohol protonation, occurring by one acidic –OH group of the zeolite fragment, followed by a concerted β-elimination to give propene. The catalytic activity is affected by the size of the zeolite cavity, which is larger in the H-Y than in the H-ZMS-5 zeolite. The adsorption energy of the reagent, as an example, decreases in the order: H-Y cavity ≃ H-ZMS-5 surface > H-ZMS-5 cavity, pointing…

Reaction mechanismChemistryDFT and MP2 calculationsPhotochemistryCatalysisReaction modelingCatalysisGibbs free energyPropenePropan-2-ol dehydrationsymbols.namesakechemistry.chemical_compoundAdsorptionSettore CHIM/03 - Chimica Generale E InorganicaReagentsymbolsPhysical and Theoretical ChemistryZSM-5ZeoliteConfinement effect
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Study of the thermal behaviour of ordered bimetallic EDTA complexes

1986

Abstract The study of the thermal behaviour of a family of isostructural ordered bimetallic MM'(EDTA)·6H 2 O complexes has been performed using TG and DTA. Formal kinetic analysis of the dehydration step has been approached using non-isothermal procedures. The resulting correlation among the calculated E a values and the cationic sizes implies a common dehydration mechanism. Copper-containing complexes show distinctive behaviour during the ligand pyrolysis processes. A mechanistic interpretation involving formation of Cu(I) and Cu(0) intermediates is furnished. The evolution of the inorganic residues in systems containing both Co and Ni is especially considered given the interest in the (Co…

Reaction mechanismChemistryStereochemistryLigandCationic polymerizationCondensed Matter Physicsmedicine.diseaseCrystallographymedicineThermal stabilityDehydrationPhysical and Theoretical ChemistryIsostructuralInstrumentationPyrolysisBimetallic stripThermochimica Acta
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Study of the thermal decomposition of bromazepan complexes with Co(II), Ni(II), Cu(II) and Zn(II)

1984

Abstract The thermal behaviour of complexes of bromazepan with Co(II), Ni(II), Cu(II) and Zn(II) was studied by thermogravimetry (TG) and differential thermal analysis (DTA). The complexes decompose in two steps: dehydration and decomposition. A correlation between the dehydration temperatures of MB2Xn and the coordinating ability of X is observed.

Reaction mechanismChemistryThermal decompositionInorganic chemistryCondensed Matter Physicsmedicine.diseaseDecompositionThermogravimetryDifferential thermal analysisThermalmedicineDehydrationPhysical and Theoretical ChemistryInstrumentationPyrolysisThermochimica Acta
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Structural insight into the reaction mechanism of Pd-catalyzed nitrile hydration: Trapping the [Pd(H2O)4]2+ cation through a supramolecular complex

2016

Abstract Four new bis(oxamato)palladate(II) complexes of formula (n-Bu4N)2[Pd(2,4,6-Me3pma)2]·2CH3CN (1), (n-Bu4N)2[Pd(2,4,6-Me3pma)2]·2CH3CONH2 (2) and (n-Bu4N)4[Pd(H2O)4][Pd(4-Xpma)2]3·2CH3CONH2 with X = Br (3) and Cl (4) (2,4,6-Me3pma = N-2,4,6-trimethylphenyloxamate, 4-Brpma = N-4-bromophenyloxamate, N-4-chlorophenyloxamate and n-Bu4N+ = tetra-n-butylammonium) have been obtained and characterized by single crystal X-ray diffraction. All of them contain bis(oxamato)palladate(II) anions and bulky n-Bu4N+ cations, but compounds 3 and 4 have also the out of the ordinary [Pd(H2O)4]2+ inorganic cation. Acetonitrile and appealing acetamide are present as lattice molecules in compounds (1) and …

Reaction mechanismNitrile010405 organic chemistryChemistryStereochemistrySupramolecular chemistryReaction intermediate010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryHydration reactionMoleculePhysical and Theoretical ChemistryAcetonitrileAcetamideInorganica Chimica Acta
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Dynamics of hyaluronan aqueous solutions as assessed by fast field cycling NMR relaxometry.

2010

Fast field cycling (FFC) NMR relaxometry has been used to study the conformational properties of aqueous solutions of hyaluronan (HYA) at three concentrations in the range 10 to 25 mg mL(-1). Results revealed that, irrespective of the solution concentration, three different hydration layers surround hyaluronan. The inner layer consists of water molecules strongly retained in the proximity of the HYA surface. Because of their strong interactions with HYA, water molecules in this inner hydration layer are subject to very slow dynamics and have the largest correlation times. The other two hydration layers are made of water molecules which are located progressively further from the HYA surface.…

RelaxometryAqueous solutionMagnetic Resonance SpectroscopyField cyclingChemistrySettore AGR/13 - Chimica AgrariaDynamics (mechanics)Analytical chemistryWaterBiochemistryAnalytical ChemistryIntramolecular forceQuadrupoleMolecular motionCarbohydrate ConformationMoleculeFFC-NMR Relaxometry Correlation time Quadrupole interactions Hydration layerHyaluronic AcidAnalytical and bioanalytical chemistry
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Ab initio modelling of oxygen vacancies and protonic defects in La1−xSrxFeO3−δ perovskite solid solutions

2016

Using hybrid density functionals, detailed ab initio calculations were performed for oxygen vacancies and protons in La1−xSrxFeO3−δ perovskite solid solutions which may serve as a cathode material in protonic ceramic fuel cells. The atomic and electronic structures of different configurations of defects and the role of Fe oxidation state are analyzed in detail. The energetics of the reduction and hydration reactions are investigated. The hydration energy is found to be significantly smaller than for Ba(Zr1−xYx)O3−x/2 electrolyte materials, and the role of basicity as one decisive factor is discussed.

Renewable Energy Sustainability and the EnvironmentChemistryInorganic chemistryAb initio02 engineering and technologyGeneral ChemistryElectrolyte010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAb initio quantum chemistry methodsOxidation statevisual_artvisual_art.visual_art_mediumPhysical chemistryGeneral Materials ScienceCeramic0210 nano-technologyHydration energyPerovskite (structure)Solid solutionJournal of Materials Chemistry A
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