Nitrogen Hydrogen Sulfide Research Articles

Equilibrium-phase properties of carbon dioxide-butane and nitrogen-hydrogen sulfide systems at subambient temperatures

To supply the data needed to perform reliable design calculations with petroleum reservoir fluids or natural gas systems, the University of Alberta determined the vapor and liquid equilibrium-phase compositions at 50.0/sup 0/, 1.1/sup 0/, and -49.3/sup 0/F for the carbon dioxide-n-butane system and at -49.3/sup 0/ and -99.4/sup 0/F for the nitrogen-hydrogen sulfide system. The data for the 50.0/sup 0/F isotherm for the carbon dioxide-n-butane system were taken in a variable-volume cell, and the remaining data in a constant-volume cell designed for operation at low temperatures. Refractive index measurements of the equilibrium phases were made for the carbon dioxide-n-butane system at 50.0/sup 0/ and 1.1/sup 0/F. These measurements were used to determine phase densities by the use of the Lorentz-Lorenz molar refractivity relationship.

Equilibrium-phase properties of nitrogen-hydrogen sulfide system

after an average of 12 expansions is 0.0024%. The relative error in the compressibility factors at intermediate pressures is then approximately 0.0024 jt for the jth expansion, becauss this error in any individual Z value is caused only by the effect of the N O error on the subsequent expansions. Therefore, the error in compressibility factor from this source at initial pressure is 0.168%. The maximum uncertainty in the extrapolation in the curve P j n i = 1 ' N L vs. P j to get the cell constant is 0.02%. When all these possible errors are considered, the Z values determined are probably accurate to f0.19%.

Compressibility factors of nitrogen-hydrogen sulfide mixtures

Compressibility factors of nitrogen-hydrogen sulfide mixtures

Experimental heat capacities of nitrogen-hydrogen sulfide mixtures at elevated pressures

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTExperimental heat capacities of nitrogen-hydrogen sulfide mixtures at elevated pressuresGerald P. Hamaliuk, P. Raj Bishnoi, and Donald B. RobinsonCite this: J. Chem. Eng. Data 1974, 19, 1, 78–81Publication Date (Print):January 1, 1974Publication History Published online1 May 2002Published inissue 1 January 1974https://doi.org/10.1021/je60060a022RIGHTS & PERMISSIONSArticle Views96Altmetric-Citations5LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (392 KB) Get e-Alerts Get e-Alerts

The Vibrational Spectra and Structure of Nitrogen Tetrasulfide

The infrared and Raman spectra of nitrogen tetrasulfide (N4S4) are presented along with the infrared spectrum of nitrogen hydrogen sulfide (N4S4H4). These data have been considered in terms of the several proposed structures for nitrogen tetrasulfide and have been found to be consistent with a cage structure of D2d symmetry. With the aid of a normal coordinate analysis of the nondegenerate symmetry species, a complete assignment of frequencies to their normal modes of vibration has been made for nitrogen tetrasulphide. A tentative assignment of frequencies is also given for nitrogen hydrogen sulfide.