THE SYSTEM ETHANOL-METHANOL AT 40 °C.

1942 ◽  
Vol 20b (10) ◽  
pp. 207-211 ◽  
Author(s):  
A. C. Morris ◽  
L. T. Munn ◽  
G. Anderson
Keyword(s):  
Partial Pressure ◽  
Total Pressure ◽  
Experimental Error ◽  
Pressure Curve ◽  
Raoult’S Law ◽  
Raoult's Law

The system ethanol-methanol was studied at 40 °C. using the original and also a modified form of the apparatus of Ferguson and Funnell. The total pressure curve is linear and the partial pressure curves agree with Raoult's law within the experimental error.

The entropy of liquid mixtures: I. The theory of Raoult's Law

1941 ◽  
Vol 60 (2) ◽  
pp. 76-84 ◽  
Author(s):  
A. J. Staverman ◽  
J. H. van Santen
Keyword(s):  
Liquid Mixtures ◽  
Raoult’S Law ◽  
Raoult's Law

Sulfidation Experiments in a Pressurized Thermogravimetric Analyzer With Chinese Calcined Limestones

2005 ◽  
Author(s):  
Zhanlong Song ◽  
Mingyao Zhang
Keyword(s):  
Partial Pressure ◽  
Reaction Temperature ◽  
Total Pressure ◽  
Volume Fraction ◽  
Nitrogen Adsorption ◽  
Reaction Rates ◽  
Thermogravimetric Analyzer ◽  
Morphological Studies ◽  
Shrinking Core ◽  
Structure Properties

The sulfidation experiments with two kinds of Chinese calcined limestones were performed in a pressurized thermogravimetric analyzer (PTGA). The effects of reaction temperature (700–950°C), total pressure (0–1MPa), particle size (0.055–2mm), and H2S concentration (0.1–4%) on the sorbent conversions were analyzed. Morphological studies with scanning electron microscope and energy dispersive spectroscopy (SEM-EDS) equipment were made to obtain the pictures of solid surface and of the cross-sectioned samples. Nitrogen adsorption measurements were applied to determine the pore structure properties of the particles. Experimental results show that the sulfidation rate increases with total pressure when the volume fraction of H2S is constant. However, the rate of sulfidation decreases with the increase of total pressure when the H2S partial pressure is constant. Reaction temperature affects the sulfidation greatly, and the reaction rate increases with temperature. The sulfidation is the first order with respect to H2S partial pressure. Moreover, larger particles result in lower conversions and reaction rates. The unreacted shrinking core model was applied to describe the sulfidation to determine the kinetic parameters.

scholarly journals Raoult’s law revisited: accurately predicting equilibrium relative humidity points for humidity control experiments

2016 ◽  
Author(s):  
Michael G. Bowler ◽  
David R. Bowler ◽  
Matthew W. Bowler
Keyword(s):  
Relative Humidity ◽  
Vapour Pressure ◽  
Control Device ◽  
Raoult’S Law ◽  
Simple Argument ◽  
Humidity Control ◽  
Saturated Vapour Pressure ◽  
Saturated Vapour ◽  
Equilibrium Relative Humidity ◽  
Raoult's Law

AbstractThe humidity surrounding a sample is an important variable in scientific experiments. Biological samples in particular require not just a humid atmosphere but often a relative humidity (RH) that is in equilibrium with a stabilizing solution required to maintain the sample in the same state during measurements. The controlled dehydration of macromolecular crystals can lead to significant increases in crystal order, which often leads to higher diffraction quality. Devices that can accurately control the humidity surrounding crystals on a beamline have led to this technique being increasingly adopted, as experiments become easier and more reproducible. Matching the relative humidity to the mother liquor is the first step to allow the stable mounting of a crystal. In previous work, we measured the equilibrium relative humidity for a range of concentrations of the most commonly used precipitants and showed how this related to Raoult’s law for the equilibrium vapour pressure of water above a solution. However, a discrepancy between measured values and those predicted by theory could not be explained. Here, we have used a more precise humidity control device to determine equilibrium relative humidity points. The new results are in agreement with Raoult’s law. We also present a simple argument in statistical mechanics demonstrating that the saturated vapour pressure of a solvent is proportional to its mole fraction in an ideal solution: Raoult’s Law. The same argument can be extended to the case where solvent and solute molecules are of different size, as is the case with polymers. The results provide a framework for the correct maintenance of the RH surrounding samples.SynopsisThe equilibrium relative humidity values for a number of the most commonly used precipitants in biological macromolecule crystallisation have been measured using a new humidity control device. A simple argument in statistical mechanics demonstrates that the saturated vapour pressure of a solvent is proportional to its mole fraction in an ideal solution (Raoult’s Law). The same argument can be extended to the case where solvent and solute molecules are of different size.

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