Search results for "yield"

showing 10 items of 1338 documents

Microreactor processing for the aqueous Kolbe-Schmitt synthesis of hydroquinone and phloroglucinol

2007

Hydroquinone and phloroglucinol were used as substrates for the aqueous Kolbe-Schmitt synthesis, using a novel processing methodology, termed high-p,T processing, recently demonstrated for the carboxylation of resorcinol. By the high-p,T approach, the temperature limitations of classical batch synthesis, e.g., set by reflux conditions (solvent boiling point), can be overcome by simple technical expenditure, e.g., the use of a few microstructured components, a capillary, and a needle valve at very low internal holdup. In this way, favorable speed-up of chemical reaction is achieved at temperatures normally outside the useful range for organic synthesis. While the hydroquinone synthesis gave …

HydroquinoneChemistryDecarboxylationGeneral Chemical EngineeringPhloroglucinolGeneral ChemistryIndustrial and Manufacturing EngineeringReaction ratechemistry.chemical_compoundCarboxylationYield (chemistry)Organic chemistryOrganic synthesisMicroreactorChemical Engineering & Technology
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Towards Large-Scale Steady-State Enhanced Nuclear Magnetization with In Situ Detection

2021

Signal Amplification By Reversible Exchange (SABRE) boosts NMR signals of various nuclei enabling new applications spanning from magnetic resonance imaging to analytical chemistry and fundamental physics. SABRE is especially well positioned for continuous generation of enhanced magnetization on a large scale, however, several challenges need to be addressed for accomplishing this goal. Specifically, SABRE requires (i) a specialized catalyst capable of reversible H2 activation and (ii) physical transfer of the sample from the point of magnetization generation to the point of detection (e.g., a high-field or a benchtop NMR spectrometer). Moreover, (iii) continuous parahydrogen bubbling accele…

IMesMagnetizationchemistry.chemical_compoundZero field NMRMaterials scienceSpectrometerchemistryYield (chemistry)EvaporationAnalytical chemistryHyperpolarization (physics)Spin isomers of hydrogen
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Fluorescence labelling of organic acidic compounds with 4-bromomethyl-7-methoxycoumarin (Br-Mmc)

1977

4-Bromomethyl-7-methoxycoumarin (Br-Mmc) is introduced as a fluorescence marker for aromatic and heterocyclic acids. To investigate the applicability of this method on substances of different chemical classes, screening experiments with 110 compounds were carried out using a microrefluxer. Most aromatic and heterocyclic monocarboxylic acids gave Mmc-esters which are fluorescent on thin-layer plates, like the Mmc-esters of fatty acids, which have been previously investigated. Strong acids, alcohols, amides and most amines did not react, whereas certain cyclic amines such as piperidine gave strongly fluorescent derivatives. Mmc-phenyl ethers shows only weak fluorescence. A new standard proced…

In situChemistrydigestive oral and skin physiologyClinical BiochemistryGeneral Medicine4-bromomethyl-7-methoxycoumarinBiochemistryFluorescenceAnalytical ChemistryCatalysischemistry.chemical_compoundYield (chemistry)LabellingOrganic chemistryGeneral Materials SciencePiperidineHeterocyclic AcidsFresenius' Zeitschrift f�r Analytische Chemie
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A new cell for the study of in situ chemical reactions using X-ray absorption spectroscopy

2005

An in situ cell for reductive and oxidative treatments at different temperatures that allows the possibility of recording data as a function of temperature has been designed and constructed for X-ray absorption experiments at the GILDA beamline BM08 of ESRF. The cell is linked to a mass quadrupole spectrometer providing control of the reaction gases and monitoring of the products. The apparatus allows measurements to be performed both in transmission and fluorescence geometry. The cell was tested by studying the CO oxidation reaction promoted by a Pt/ceria-zirconia-supported catalyst. The CO(2) yield is correlated with the structural results confirming the existence of a strong metal-suppor…

In situNuclear and High Energy PhysicsAnalytical chemistryChemical reactionRedoxCatalysisSpecimen HandlingCatalysisthree-way catalystX-Ray DiffractionAbsorption (electromagnetic radiation)InstrumentationPlatinumX-ray absorption spectroscopyRadiationSpectrometerChemistryTemperatureSpectrometry X-Ray EmissionCarbon Dioxidein situ EXAFSOxygenYield (chemistry)Flow Injection AnalysisZirconiumOxidation-Reductionstrong metal support interaction
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"dataFig4_V0" of "Multiplicity dependence of J/$\psi$ production at midrapidity in pp collisions at $\sqrt{s}$ = 13 TeV"

2020

$N_{J/psi}/ / N_{ch}/$, $|y^{J/\psi}|<0.9$, $p_{T}^{J/\psi}$ integrated, event selection V0

Inclusive J/PSI13000.0$N_{J/psi}/_{INEL>0}$ $p_{T}$ integratedNormalized YieldP P --> J/PSI < E+ E- > XHigh Energy Physics::ExperimentNormalized Nch Dependence
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"dataFig4_SPD" of "Multiplicity dependence of J/$\psi$ production at midrapidity in pp collisions at $\sqrt{s}$ = 13 TeV"

2020

$N_{J/psi}/ / N_{ch}/$, $|y^{J/\psi}|<0.9$, $p_{T}^{J/\psi}$ integrated, event selection SPD

Inclusive J/PSI13000.0$N_{J/psi}/_{INEL>0}$ $p_{T}$ integratedNormalized YieldP P --> J/PSI < E+ E- > XPhysics::Accelerator PhysicsHigh Energy Physics::ExperimentNormalized Nch Dependence
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"Table 35" of "Measurement of $J/\psi$ at forward and backward rapidity in $p+p$, $p+A$l, $p+A$u, and $^3$He$+$Au collisions at $\sqrt{s_{_{NN}}}=200…

2020

J/psi invariant yields in 3He+Au collisions as a function of pT and centrality at forward rapidity. The statistical and systematic uncertainties vary point-to-point and are listed for each measured value. An additional global systematic uncertainty is provided in each column heading, which applies to all data points per column.

InclusiveInv. YieldJ/psi --> mu+mu-200.0
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"Table 27" of "Measurement of $J/\psi$ at forward and backward rapidity in $p+p$, $p+A$l, $p+A$u, and $^3$He$+$Au collisions at $\sqrt{s_{_{NN}}}=200…

2020

J/psi invariant yields as a function of rapidity in small systems. The statistical and systematic uncertainties vary point-to-point and are listed for each measured value. An additional global systematic uncertainty is provided in each column heading, which applies to all data points per column.

InclusiveInv. YieldJ/psi --> mu+mu-200.0
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"Table 29" of "Measurement of $J/\psi$ at forward and backward rapidity in $p+p$, $p+A$l, $p+A$u, and $^3$He$+$Au collisions at $\sqrt{s_{_{NN}}}=200…

2020

J/psi invariant yields in p+Au collisions as a function of centrality and apidity. The statistical and systematic uncertainties vary point-to-point and are listed for each measured value. An additional global systematic uncertainty is provided in each column heading, which applies to all data points per column.

InclusiveInv. YieldJ/psi --> mu+mu-200.0
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"Table 28" of "Measurement of $J/\psi$ at forward and backward rapidity in $p+p$, $p+A$l, $p+A$u, and $^3$He$+$Au collisions at $\sqrt{s_{_{NN}}}=200…

2020

J/psi invariant yields in p+Al collisions as a function of centrality and rapidity. The statistical and systematic uncertainties vary point-to-point and are listed for each measured value. An additional global systematic uncertainty is provided in each column heading, which applies to all data points per column.

InclusiveInv. YieldJ/psi --> mu+mu-200.0
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