Liquid-Vapour Equilibria. II. The System Benzene-n-heptane

Brown, I; Ewald, A. H.

doi:10.1071/ch9510198

Cited by 18 publications

(17 citation statements)

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“…(b) Purification a d Properties of Comportemts The ethanol was purified by the method of Barker, Brown, and Smith (1953) and the benzene as described by Brown and Ewald (1951). The physical properties of the components are shown in Table 1.…”

Section: Introductionmentioning

confidence: 99%

Liquid-Vapour equilibria. IV. The system ethanol + benzene at 45°C

Brown¹,

Smith²

1954

Aust. J. Chem.

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Section: Introductionmentioning

confidence: 99%

Liquid-Vapour equilibria. IV. The system ethanol + benzene at 45°C

Brown¹,

Smith²

1954

Aust. J. Chem.

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“…(1955) Freshwater and Pike (1967) Severns, et a l . (1955) Susarev and Ch'En Shu-Tzu (1963) Brown and Ewald (1951) Brown and Smith (1954b) Nagata, et a l . (1970,1973) Severns, et a l .…”

Section: Binary Vapor-liquid Equilibriamentioning

confidence: 97%

On the Palmer-Smith Equation

Nagata¹,

Gotoh²

1975

Ind. Eng. Chem. Proc. Des. Dev.

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The Palmer-Smith equation is tested in t h e correlation of vapor-liquid equilibrium data of various binary and ternary systems.Combination of the local composition idea suggested by Wilson (1964) and the two-liquid theory of Scott (1956) leads to two different equations applicable to partially miscible systems as well as totally miscible systems. One of them is the nonrandom two-liquid (NRTL) equation derived by Renon and Prausnitz (1968) and the other is proposed by Palmer and Smith (1972). These equations differ from each other in the assumed form of the weighting function to define local compositions. The suitability of NRTL equations was studied in several investigations. Palmer and Smith did not test their proposed equation extensively with a wide variety of systems. This work presents results of such a test.

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“…Furthermore, there might be potential toxicity and side effects on human organism, e.g. insomnia, tachycardia, cerebral haemorrhage, or heart attack [18][19][20][21] related to the use of DMAA, especially in combination with alcohol or other ingredients occurring in the DMAA-containing products such as caffeine.…”

Section: Introductionmentioning

confidence: 99%

Enantiomeric separation of 1,3‐dimethylamylamine by capillary electrophoresis with indirect UV detection using a dual‐selector system

et al. 2015

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The CE method employing an indirect UV detection for the enantioseparation of 1,3-dimethylamylamine (DMAA), widely used in various preworkout and dietary supplements labeled as a constituent of geranium extract has been developed. The dual-selector system consisting of negatively charged sulfated α-CD (1.1% w/v) and sulfated β-CD (0.2% w/v) in 5 mM phosphate/Tris buffer (pH 3.0) containing the addition of 10 mM benzyltriethylammonium chloride (BTEAC) as the chromophoric additive was used for the enantiomeric separation of DMAA stereoisomers with the LODs in the range of 7.82-9.24 μg/mL. The method was partly validated and applied for the determination of the stereoisomeric composition of DMAA in commercial dietary supplements to verify the potential natural origin of DMAA.

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Liquid-Vapour Equilibria. II. The System Benzene-n-heptane

Cited by 18 publications

References 0 publications

Liquid-Vapour equilibria. IV. The system ethanol + benzene at 45°C

Liquid-Vapour equilibria. IV. The system ethanol + benzene at 45°C

On the Palmer-Smith Equation

Enantiomeric separation of 1,3‐dimethylamylamine by capillary electrophoresis with indirect UV detection using a dual‐selector system

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