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Hexane

About: Hexane is a research topic. Over the lifetime, 3759 publications have been published within this topic receiving 57996 citations. The topic is also known as: CH3-[CH2]4-CH3 & hexyl hydride.


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Journal ArticleDOI
TL;DR: In this paper, a series of dead-end hydrogenation runs were conducted at temperatures from 115 to 145°C, at hydrogen partial pressures from 44 to 74 p.s.i.
Abstract: Refined and bleached cottonseed oil was dissolved in a solvent (hexane, isopropyl alcohol, or di-isopropyl ether) and was then hydrogenated in a dead-end hydrogenator. Hydrogenation runs were conducted at temperatures from 115 to 145°C., at hydrogen partial pressures from 44 to 74 p.s.i.a., with catalyst concentrations varying from 0.05 to 0.40% nickel, and at high rates of agitation to climinate mass-transfer resistances. A series of hydrogenation runs was also made in which no solvent was used. The rates of hydrogenation for the various series of runs were in the same order of magnitude but decreased in the following order: nonsolvent, hexane, isopropyl alcohol, and di-isopropyl other runs. Selectivity and isomerization were low in all cases and essentially identical for solvent and nonsolvent runs. The rate of hydrogenation increased in all cases with higher catalyst concentrations. For the isopropanol runs, the reaction rate was maximum as a function of temperature at about 135°C. In the case of the other solvents, the rate of hydrogenation increased with increased temperature in the range from 115 to 145°C., but the rate increases of the solvent runs were less than those of the nonsolvent runs.

21 citations

Journal ArticleDOI
TL;DR: Azido cellulose phenylcarbamate (AzCPC) was synthesized regioselectively and chemically immobilized onto aminized silica gel to afford urea-bonded chiral stationary phases (CSPs).

20 citations

Journal ArticleDOI
01 Feb 1984
TL;DR: In this paper, the adsorption of hexene-1/n-hexane mixtures of liquid solution on an NaX-zeolite (Si Al = 1.4 ) was studied.
Abstract: The adsorption of hexene-1/ n -hexane mixtures of liquid solution on an NaX-zeolite ( Si Al = 1.4 ) was studied. The excess isotherms and the heats of immersion were determined on this zeolite. The difference between the molar heats of immersion determined from the temperature dependence of the surface excess is −32.4 kJ/mole the comparable value obtained by calorimetric method is −33.4 kJ/mole. A detailed thermodynamic analysis of these data showed an ideal behavior of hexene-1/ n -hexane in the bulk phase and adsorbed phase. A thermodynamic consistency test for the adsorption of liquids and their vapors was applied to our system.

20 citations

Journal ArticleDOI
TL;DR: In this paper, the ability of binary deep eutectic solvent choline chloride+1,2-propanediol (DES1; 1 : 3 mole ratio) and ternary deep euectic solvents (DES2) for breaking the azeotropes hexane/heptane+ethanol by means of liquid-liquid extraction was evaluated.
Abstract: The ability of binary deep eutectic solvent choline chloride+1,2-propanediol (DES1; 1 : 3 mole ratio) and ternary deep eutectic solvent choline chloride+1,2-propanediol+water (DES2; 1 : 3 : 3 mole ratio) for breaking the azeotropes hexane/heptane+ethanol by means of liquid-liquid extraction was evaluated. Liquid-liquid equilibrium experiments were performed at 298.15 K, at atmospheric pressure, and data were correlated by NRTL and UNIQUAC models. Thermodynamic properties (density, viscosity, refractive index and speed of sound) of DES1 and DES2 were determined in temperature range from 288.15 K to 333.15 K and at atmospheric pressure. Extraction ability of the investigated eutectics yielded promising results in comparison with conventional solvents. Besides a high selectivity towards ethanol, an advantage of DES2 is its lower viscosity and higher distribution ratio values, which is an important aspect for a potential industrial application. Another advantage of both investigated eutectics is their easy and high recoverability from the extract layer based on their negligible vapor pressure.

20 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023205
2022429
202186
202092
201999
201891