Showing papers on "Hexane published in 1968"
67 citations
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TL;DR: In this article, the Hammett equation was used to correlate trialkyl phosphate dimerization constants for wet and dry hexane, suggesting the non-existence of a strongly bonded monohydrate, like (BuO)3PO·H2O.
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TL;DR: In this paper, the Gibbs adsorption equation was used to calculate the composite and individual adsorment isotherms at the liquid-vapor interface for mixtures of benzene with n -hexane, 2,2,4-trimethylpentane, and n -dodecane.
TL;DR: In this article, the partition coefficient of the methyl ester and the mutual solubility of hexane and acetonitrile, at each temperature, varied with ester concentration in the system.
Abstract: Ternary diagrams for methyl oleate/hexane/acetonitrile and methyl palmitate/hexane/acetonitrile systems were constructed from equilibria data obtained at 20.0 and 30.4C. The diagrams varied significantly with temperature; both systems showed expanded regions of immiscibility at the lower temperature. Both the partition coefficient of the methyl ester and the mutual solubility of hexane and acetonitrile, at each temperature, varied with ester concentration in the system. At high ester concentration, an inversion of the phases was observed. The countercurrent distribution of these compounds, as influenced by these effects, is discussed.
TL;DR: In this paper, the volumes of mixing of hexadecane and each of the isomers of hexane have been measured for the equimolar mixtures at 20°C.
Abstract: The volumes of mixing of hexadecane and each of the isomers of hexane have been measured for the equimolar mixtures at 20°C. The results have been used together with previously measured values of ΔH to obtain ΔUv.
A very good correlation is found between the energy of mixing and the properties of the pure alkanes.
01 Jan 1968
TL;DR: In this paper, the authors present a set of rules for the use of Hexane hexagons in the context of human-computer interaction. But they do not specify how to use them in a real world scenario.
Abstract: C H A P T E R L IN T R O D U C T IO N ........................................ ........................................... I II. L IT E R A T U R E SU R V E Y ........................................................................ 4 A. C ry s ta l l in e Z e o l i t e s .................................................................... 4 B. H y d r o c r a c k in g ................................................................................ 15 C. P r o d u c t s f r o m Hexane H y d ro c ra c k in g .................. 29 D. P r o d u c t s f r o m C yclohexane H y d ro c ra c k in g .................... 35 E . C o n c lu s io n s f r o m the L i t e r a tu r e S u r v e y ......................... 37 HL E X P E R IM E N T A L EQ U IPM E N T AND PR O C E D U R E ............. 38 A. G e n e r a l ............................................................................................... 38 B. E q u ip m e n t .......................................................................................... 38 C. M a t e r i a l s .......................................................................................... 43 D. P r o c e d u r e .......................................................................................... 46 IV. KINETIC M O D E L .................................................................................... 49 A. In i t ia l S im p lif ied M o d e l .............................................................. 49 B. L a n g m u ir -H in sh e lw o o d E q u a t io n s ................................ 53