Search results for "Calorimetry"

showing 10 items of 504 documents

Lindblad equation approach for the full counting statistics of work and heat in driven quantum systems

2013

We formulate the general approach based on the Lindblad equation to calculate the full counting statistics of work and heat produced by driven quantum systems weakly coupled with a Markovian thermal bath. The approach can be applied to a wide class of dissipative quantum systems driven by an arbitrary force protocol. We show the validity of general fluctuation relations and consider several generic examples. The possibilities of using calorimetric measurements to test the presence of coherence and entanglement in the open quantum systems are discussed. QC 20141010

Hot TemperatureQuantum simulatorFOS: Physical sciencesresonance fluorescenceQuantum entanglementCalorimetry01 natural sciences010305 fluids & plasmasOpen quantum system0103 physical sciencesStatisticsFysikStatistical physicsequality010306 general physicsQuantum statistical mechanicsPhysicsQuantum discordQuantum Physicsta114Lindblad equationModels TheoreticalClassical mechanicsPhysical SciencesDissipative systemQuantum TheoryQuantum algorithmfluctuation theoremQuantum Physics (quant-ph)
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Chip calorimetry for the monitoring of whole cell biotransformation

2005

Abstract Efficient control of whole cell biotransformation requires quantitative real-time information about the thermodynamics and kinetics of growth and product formation. Heat production contains such information, but its technical application is restricted due to the high price of calorimetric devices, the difficulty of integrating them into existing bioprocesses and the slow response times of established microcalorimeters. A new generation of chip or nanocalorimeters may overcome these weaknesses. We thus tested a highly sensitive chip calorimeter for its applicability in biotechnological monitoring. It was used to monitor aerobic growth of suspended and immobilized Escherichia coli DH…

Hot TemperatureTime FactorsAnalytical chemistryBioengineeringCalorimetryCalorimetryModels BiologicalApplied Microbiology and BiotechnologyBiotransformationEscherichia coliProcess controlAnaerobiosisBioprocessProcess engineeringBiotransformationCells CulturedChemistrybusiness.industryGeneral MedicineChipCalorimeterKineticsThermodynamicsHalomonasbusinessWhole cellBiosensorBiotechnologyJournal of Biotechnology
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Simultaneous application of Fourier transform Raman spectroscopy and differential scanning colorimetry for the in situ investigation of phase transit…

1991

Abstract The combination of Fourier transform Raman spectroscopy with differential scanning colorimetry for the in situ investigation of phase transitions is illustrated using ammonium nitrate as an example. This method helps unambiguous characterisation of different phases by providing a simultaneous probe of thermodynamic and vibrational data.

In situPhase transitionChemistryGeneral EngineeringAnalytical chemistryColorimetry (chemical method)symbols.namesakeFourier transformDifferential scanning calorimetrysymbolsSpectroscopyRaman spectroscopyPhysics::Atmospheric and Oceanic PhysicsDifferential (mathematics)Spectrochimica Acta Part A: Molecular Spectroscopy
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A standard calculation methodology for human doubly labeled water studies.

2021

Summary The doubly labeled water (DLW) method measures total energy expenditure (TEE) in free-living subjects. Several equations are used to convert isotopic data into TEE. Using the International Atomic Energy Agency (IAEA) DLW database (5,756 measurements of adults and children), we show considerable variability is introduced by different equations. The estimated rCO2 is sensitive to the dilution space ratio (DSR) of the two isotopes. Based on performance in validation studies, we propose a new equation based on a new estimate of the mean DSR. The DSR is lower at low body masses (<10 kg). Using data for 1,021 babies and infants, we show that the DSR varies non-linearly with body mass betw…

IndirectFuture studiesBODY-WATER030309 nutrition & dietetics[SDV]Life Sciences [q-bio]Body waterINFANTS030209 endocrinology & metabolismDoubly labeled watertotal energy expenditureCarbon dioxide productionCalorimetryOxygen IsotopesCalorimetryArticleGeneral Biochemistry Genetics and Molecular BiologyRC120003 medical and health sciences0302 clinical medicineTotal energy expendituredoubly labeled water; free-living; total energy expenditure; validationStatisticsINDIRECT CALORIMETRYRange (statistics)O-18HumansObesity(H2O)-H-2-O-18 METHODCARBON-DIOXIDE PRODUCTIONComputingMilieux_MISCELLANEOUSMathematicsCO2 PRODUCTIONH-2validation0303 health sciencesfree-livingDILUTION SPACE RATIOENERGY-EXPENDITUREWaterCalorimetry IndirectDeuterium6. Clean waterdoubly labeled waterDilutionIAEA DLW database groupBody Composition1182 Biochemistry cell and molecular biologyEnergy Metabolism
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Pressure Effect Studies on the Spin‐Transition Behavior of a Dinuclear Iron(II) Compound

2013

Magnetic studies into the effect of different hydrostatic pressures between ambient and 1.03 GPa on the high-spin (HS) i low-spin (LS) transition behavior of the dinuclear iron(II) compound [Fe II 2(PMAT)2](BF4)4·DMF (1, PMAT = 4-amino3,5-bis{[(2-pyridylmethyl)amino]methyl}-4H-1,2,4-triazole, DMF = N,N-dimethylformamide) have been carried out at 2– 300 K. Under ambient pressure, the sample studied exhibits a [HS–HS] to [HS–LS] half spin transition (ST) at T½ = 208 K without any thermal hysteresis. Increasing the pressure above 0.2 GPa causes an increase (initially rapid but above 0.5 GPa more gradual) of T½ as well as a matching reduction in the residual high-spin fraction at room temperatu…

Inorganic ChemistryCrystallographyThermal hysteresisNuclear magnetic resonanceChemistrySpin crossoverSpin transitionCalorimetryAmbient pressureEuropean Journal of Inorganic Chemistry
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4,4′‐Distyrylazobenzol als Mesogen

1992

4,4′-Distyrylazobenzene as Mesogen From 3,4-dihydroxybenzaldehyde (1) the tetraalkoxy-substituted 4,4′-distyrylazobenzenes (E,E,E)-5a – c are synthesized. A similar reaction sequence leads from ethyl 3,4,5-trihydroxy-benzoate (6) to the hexaalkoxy-substituted 4,4′-distyrylazobenzenes (E,E,E)-11 b, c. With the exception of 5a all products show thermotropic LC properties. Smectic phases have been characterized by polarizing microscopy and by differential scanning calorimetry.

Inorganic ChemistryCrystallographychemistry.chemical_compoundDifferential scanning calorimetryAzo compoundReaction sequenceChemistryLiquid crystalMesogenOrganic chemistryThermotropic crystalPolarizing microscopyChemische Berichte
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Cooperative Spin‐Crossover Behaviour in Polymeric 1D Fe II Coordination Compounds: [{Fe(tba) 3 }X 2 ]· n H 2 O

2007

A new family of 1D cooperative spin-crossover polymers with general formula [{Fe(tba)3}X2]·nH2O [tba = N-(4H-1,2,4-triazol-4-yl)benzamide; X = CF3SO3–, n = 2 (1), n = 0 (4); BF4–,n = 3 (2), n = 0 (5); 4-CH3C6H4SO3–, n = 3 (3), n = 0 (6)] has been synthesised and characterised using a series of spectroscopic methods, X-ray powder diffraction, magnetic susceptibility measurements and differential scanning calorimetry. The copper analogue of 1, [{Cu(tba)3}(CF3SO3)2]·3H2O (7), has also been synthesised and its crystal structure solved at 293 K. Compound 7 crystallises in the P space group. The bidentate N-(4H-1,2,4-triazol-4-yl)benzamide ligand bridges the copper ions through the 1,2-nitrogen p…

Inorganic Chemistrychemistry.chemical_classificationCrystallographyDifferential scanning calorimetryDenticitychemistryExtended X-ray absorption fine structureStereochemistrySpin crossoverSpin transitionCrystal structureMagnetic susceptibilityCoordination complexEuropean Journal of Inorganic Chemistry
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Sequestering ability of some chelating agents towards methylmercury(II).

2013

A study on the interactions between CH3Hg+ and some S, N and O donor ligands (2-mercaptopropanoic acid (thiolactic acid (H2 TLA)), 3-mercaptopropanoic acid (H2 MPA), 2-mercaptosuccinic acid (thiomalic acid (H3 TMA)), d,l-penicillamine (H2 PSH), l-cysteine (H2 CYS), glutathione (H3 GSH), N,N′-bis(3-aminopropyl)-1-4-diaminobutane (spermine (SPER)), 1,2,3,4,5,6-benzenehexacarboxylic acid (mellitic acid (H6 MLT)) and ethylenediaminetetraacetic acid (H4 EDTA)) is reported. The speciation models in aqueous solution and the possible structures of the complexes formed are discussed on the basis of potentiometric, calorimetric, UV spectrophotometric and electrospray mass spectrometric results. For t…

Inorganic chemistryElectrospray ionisation mass spectrometry (ESI-MS)Ethylenediaminetetraacetic acidCalorimetryBiochemistrySequestering ability of S N and O donor ligandAnalytical Chemistrychemistry.chemical_compoundHydrolysisSettore CHIM/01 - Chimica AnaliticaChelationMellitic acidThiomalic acidEnvironmental Restoration and RemediationChelating AgentsThiolactic acidAqueous solutionMolecular StructureLigandMethylmercury(II) cationMethylmercury CompoundsKineticschemistryMethylmercury(II) cation; Sequestering ability of S; N and O donor ligands; UV–spectrophotometry; Electrospray ionisation mass spectrometry (ESI-MS); PotentiometryPotentiometryEnvironmental PollutantsUV–spectrophotometryNuclear chemistryAnalytical and bioanalytical chemistry
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Selective adsorption of formaldehyde and water vapors in NaY and NaX zeolites

2019

International audience; Coadsorption of formaldehyde and water vapors on NaX and NaY zeolites is studied at 298 K in the pressure range 0-2 hPa by manometry coupled with gas phase chromatography and calorimetry. Coadsorption isotherms, adsorption selectivities and coadsorption heats are measured. Results show that the coadsorption process is selective for water at low filling and for formaldehyde at high filling. The adsorption selectivity for formaldehyde over water is however too low to consider the possibility of using such adsorbents for the development of air handling units. On the other hand, a preliminary study carried out on the adsorption of formaldehyde and water in pure gas phase…

Inorganic chemistrywaterFormaldehyde02 engineering and technologyCalorimetry010402 general chemistry01 natural sciencesHigh silicaAdsorption selectivityPressure rangechemistry.chemical_compoundAdsorptionCoadsorption;Formaldehyde;Water;Zeolite;Selectivity[CHIM]Chemical SciencesGeneral Materials SciencezeoliteZeoliteComputingMilieux_MISCELLANEOUSChemistrycoadsorptionselectivityGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryMechanics of MaterialsSelective adsorptionformaldehyde0210 nano-technology
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Physico-chemical state influences in vitro release profile of curcumin from pectin beads

2014

International audience; Curcumin is a polyphenolic compound with diverse effects interesting to develop health benefit products but its formulation in functional foods or in food supplement is hampered by its poor water solubility and susceptibility to alkaline conditions, light, oxidation and heat. Encapsulation of curcumin could be a mean to overcome these difficulties. In this paper, curcumin was encapsulated by ionotropic gelation method in low methoxyl pectin beads associated with different surfactants: Solutol®, Transcutol® and sodium caseinate. After encapsulation, physico-chemical properties of encapsulated curcumin such as its solubility, physical state, tautomeric forms and encaps…

Ionotropic gelation methodfood.ingredientCurcuminPectinChemical PhenomenaChemistry Pharmaceutical02 engineering and technologyMicelleFLIM studiesMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compoundColloid and Surface ChemistryfoodAnimals[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyPhysical and Theoretical ChemistrySolubility030304 developmental biology0303 health sciencesAqueous solutionChromatographyCalorimetry Differential ScanningChemistryStereoisomerismSurfaces and InterfacesGeneral MedicineIn vitro release021001 nanoscience & nanotechnologyMicrospheresBody FluidsRatsSolventKineticsMicroscopy FluorescenceSolubilityPolyphenolCurcuminPectinsEncapsulation0210 nano-technologyPhysico-chemical stateBiotechnology
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