• Volume/Page
  • Keyword
  • DOI
  • Citation
  • Advanced
   
 
 
 

Flickr Twitter iResearch App Facebook

Year Range: 
Search Issue | RSS Feeds RSS
Previous Issue

Dec 2012

Volume 41, Issue 4, Articles (04xxxx)

back to top
RSS Feeds

A Review on Prediction Methods for Molar Enthalpies of Vaporization of Hydrocarbons: The ELBA Method as the Best Answer

Rui C. Santos and João P. Leal

J. Phys. Chem. Ref. Data 41, 043101 (2012); http://dx.doi.org/10.1063/1.4754596 (19 pages)

Online Publication Date: 26 October 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
A review on prediction methods for molar enthalpies of vaporization at T = 298.15 K of hydrocarbons is presented. A new method is proposed and compared with six of the most common used ones from the literature. This new method, the extended Laidler bond additivity (ELBA), was applied to the prediction of standard molar enthalpies of vaporization of hydrocarbons (alkanes, alkenes, alkynes, polyenes, poly-ynes, cycloalkanes, cycloalkenes, benzene compounds, biphenyl compounds, and polyphenyl compounds) at T = 298.15 K. A total of 260 experimental standard molar enthalpies of vaporization at T = 298.15 K were used for the parameters optimization. Comparison between the experimental values and those calculated using ELBA led to an average absolute difference of 0.35 kJ mol−1, corresponding to an average relative error of 0.92%. In addition, this new method proves to be better than the ones used for comparison with an independent set of 83 experimental standard molar enthalpies of vaporization at T = 298.15 K.
Show PACS
82.60.Cx Enthalpies of combustion, reaction, and formation
64.70.F- Liquid-vapor transitions
01.30.Kj Handbooks, dictionaries, tables, and data compilations
01.30.Rr Surveys and tutorial papers; resource letters

Reference Correlation of the Thermal Conductivity of Benzene from the Triple Point to 725 K and up to 500 MPa

M. J. Assael, E. K. Mihailidou, M. L. Huber, and R. A. Perkins

J. Phys. Chem. Ref. Data 41, 043102 (2012); http://dx.doi.org/10.1063/1.4755781 (9 pages) | Cited 2 times

Online Publication Date: 26 October 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
This paper contains new, representative reference equations for the thermal conductivity of benzene. The equations are based in part upon a body of experimental data that have been critically assessed for internal consistency and for agreement with theory whenever possible. In the case of the dilute-gas thermal conductivity, a theoretically based correlation was adopted in order to extend the temperature range of the experimental data. Moreover, in the critical region, the experimentally observed enhancement of the thermal conductivity is well represented by theoretically based equations containing just one adjustable parameter. The correlations are applicable for the temperature range from the triple point to 725 K and pressures up to 500 MPa. The overall uncertainty (considered to be estimates of a combined expanded uncertainty with a coverage factor of two) of the proposed correlation is estimated, for pressures less than 350 MPa and temperatures less than 725 K, to be less than 4.4%.
Show PACS
51.20.+d Viscosity, diffusion, and thermal conductivity
64.60.F- Equilibrium properties near critical points, critical exponents

Energy Levels and Observed Spectral Lines of Neutral and Singly Ionized Chromium, Cr I and Cr II

E. B. Saloman

J. Phys. Chem. Ref. Data 41, 043103 (2012); http://dx.doi.org/10.1063/1.4754694 (196 pages)

Online Publication Date: 30 November 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
The energy levels and observed spectral lines of neutral and singly ionized chromium atoms have been compiled. Tables of energy levels and spectral lines are generated for each stage. Experimental g-factors and leading percentages are included when available. An experimental value for the ionization energy for each stage is provided.
Show PACS
34.50.Fa Electronic excitation and ionization of atoms (including beam-foil excitation and ionization)
31.30.js Corrections to bound-electron g factor
32.70.Fw Absolute and relative intensities

Recommended Viscosities of 11 Dilute Gases at 25 °C

Robert F. Berg and Michael R. Moldover

J. Phys. Chem. Ref. Data 41, 043104 (2012); http://dx.doi.org/10.1063/1.4765368 (10 pages) | Cited 1 time

Online Publication Date: 13 December 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
Commercially manufactured meters that measure the flow of a process gas are often calibrated with a known flow of a surrogate gas. This requires an accurate model of the flow meter and accurate values of the relevant thermophysical properties for both gases. In particular, calibrating a “laminar” flow meter near ambient temperature and pressure requires that the ratio (process gas viscosity)/(surrogate gas viscosity) be known to approximately 0.1%. With this motivation, we critically reviewed measurements of viscosity conducted with 18 instruments near 25 °C and zero density for 11 gases: He, Ne, Ar, Kr, Xe, H2, N2, CH4, C2H6, C3H8, and SF6. For these gases and this single state, we determined viscosity ratios with relative standard uncertainties ranging from 2.7 × 10−4 to 3.6 × 10−4 at a 68% confidence level. Anchoring the ratios to the value (19.8253 ± 0.0002) × 10−6 Pa s for the viscosity of helium calculated ab initio at 25 °C and zero density yields recommended values for the other ten gases and establishes a scale for gas viscosities that is more accurate than most of the reported values. To facilitate the extension of this scale, we recommend that researchers who calibrate gas viscometers (1) use helium as a calibration gas when possible, (2) report the values of all calibration data, and (3) report the uncertainties of their measured viscosity ratios. Similarly, we recommend that data archives capture this relevant calibration information.
Show PACS
51.20.+d Viscosity, diffusion, and thermal conductivity
83.85.Jn Viscosity measurements

Recommended Correlations for the Surface Tension of Common Fluids

A. Mulero, I. Cachadiña, and M. I. Parra

J. Phys. Chem. Ref. Data 41, 043105 (2012); http://dx.doi.org/10.1063/1.4768782 (13 pages) | Cited 1 time

Online Publication Date: 19 December 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
Available values of the surface tension of 81 common fluids were fitted by using the same model presently used in the REFPROP program V9.0 by NIST. A set of data was built for every fluid by including mainly those values given in the DIPPR and DETHERM databases. For some fluids, other available sources of data were added in order to obtain adequate sets. For every fluid, we checked the accuracy of the REFPROP program and we made a new fit in order to improve the performance of the correlation. We found good general agreement between the REFPROP predictions and the data for 44 fluids, and therefore only very slight improvements are made for them. For the other 37 fluids, the REFPROP correlation can be more clearly improved. In particular, our new correlation is significantly more accurate for ammonia, deuterium, ethanol, and neon, because the version of REFPROP used gives values in clear disagreement with other data sources.
Show PACS
68.03.Cd Surface tension and related phenomena

IUPAC-NIST Solubility Data Series. 96. Amines with Water Part 1. C4–C6 Aliphatic Amines

Marian Góral, David G. Shaw, Andrzej Mączyński, Barbara Wiśniewska-Gocłowska, and Paweł Oracz

J. Phys. Chem. Ref. Data 41, 043106 (2012); http://dx.doi.org/10.1063/1.4755288 (40 pages)

Online Publication Date: 19 December 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
The mutual solubilities and related liquid-liquid equilibria of 24 binary systems of C4–C6 aliphatic amines with water are exhaustively and critically reviewed. Reports of experimental determination of solubility that appeared in the primary literature prior to the end of 2010 are compiled. For ten systems, sufficient data are available to allow critical evaluation. All data are expressed as mass percent and mole fraction as well as the originally reported units.
Show PACS
64.75.Bc Solubility

IUPAC-NIST Solubility Data Series. 96. Amines with Water Part 2. C7–C24 Aliphatic Amines

Marian Góral, David G. Shaw, Andrzej Mączyński, Barbara Wiśniewska-Gocłowska, and Paweł Oracz

J. Phys. Chem. Ref. Data 41, 043107 (2012); http://dx.doi.org/10.1063/1.4755953 (34 pages) | Cited 1 time

Online Publication Date: 19 December 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
The mutual solubilities and related liquid-liquid equilibria of 41 binary systems of C7–C24 aliphatic amines with water are exhaustively and critically reviewed. Reports of experimental determination of solubility that appeared in the primary literature prior to the end of 2010 are compiled. For seven systems, sufficient data are available to allow critical evaluation. All data are expressed as mass percent and mole fraction as well as the originally reported units.
Show PACS
64.75.Bc Solubility
01.30.Rr Surveys and tutorial papers; resource letters
64.60.F- Equilibrium properties near critical points, critical exponents

IUPAC-NIST Solubility Data Series. 96. Amines with Water Part 3. Non-Aliphatic Amines

Marian Góral, David G. Shaw, Andrzej Mączyński, Barbara Wiśniewska-Gocłowska, and Paweł Oracz

J. Phys. Chem. Ref. Data 41, 043108 (2012); http://dx.doi.org/10.1063/1.4756039 (52 pages)

Online Publication Date: 21 December 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
The mutual solubilities and related liquid-liquid equilibria of 36 binary systems of non-aliphatic amines with water are exhaustively and critically reviewed. Reports of experimental determination of solubility that appeared in the primary literature prior to the end of 2010 are compiled. For 13 systems, sufficient data are available to allow critical evaluation. All data are expressed as mass percent and mole fraction as well as the originally reported units.
Show PACS
64.75.Bc Solubility
82.60.Hc Chemical equilibria and equilibrium constants

CODATA Recommended Values of the Fundamental Physical Constants: 2010

Peter J. Mohr, Barry N. Taylor, and David B. Newell

J. Phys. Chem. Ref. Data 41, 043109 (2012); http://dx.doi.org/10.1063/1.4724320 (84 pages) | Cited 1 time

Online Publication Date: 28 December 2012

Full Text: Read Online (HTML) | Download PDF

Show Abstract
This paper gives the 2010 self-consistent set of values of the basic constants and conversion factors of physics and chemistry recommended by the Committee on Data for Science and Technology (CODATA) for international use. The 2010 adjustment takes into account the data considered in the 2006 adjustment as well as the data that became available from 1 January 2007, after the closing date of that adjustment, until 31 December 2010, the closing date of the new adjustment. Further, it describes in detail the adjustment of the values of the constants, including the selection of the final set of input data based on the results of least-squares analyses. The 2010 set replaces the previously recommended 2006 CODATA set and may also be found on the World Wide Web at physics.nist.gov/constants.
Show PACS
06.20.Jr Determination of fundamental constants
02.70.Rr General statistical methods
33.15.-e Properties of molecules
32.30.-r Atomic spectra
Close
Google Calendar
ADVERTISEMENT

close