Viscosity and density of some aliphatic, cyclic, and aromatic hydrocarbons binary liquid mixtures

Abstract

Literature Cited(1) Bernardo-Gil, M. G.; Ribeiro, . A. Fluid Phase Equil., in (2) Bernardo-Gil, M. G.; Ribeiro, . A. Submitted for publication.(3) Handbook of Chemistry and Physics, 57th ed.; Weast, R., Ed.; CRC Press: Cleveland, OH, 1977.

Densities and Kinematic Viscosities of a Quinary Regular Liquid System and Its Five Quaternary Subsystems at 293.15 K and 298.15 K

“…The McAllister three-body model, as reported by Nhaesi and Asfour [2], can predict the viscosities of an n-component mixture according to the following equation: [15] 0.683 75 [12] 0.6023 0.6022 [15] 0.6096 [12] 0.4120 0.4117 [15] Octane 0.7025 0.7022 [15] 0.702 67 [12] 0.7734 0.771 [15] 0.7758 [12] 0.5433 0.5414 [15] Toluene 0.8667 0.8668 [15] 0.8760 [17] 0.6797 0.6767 [15] 0.6786 [18] 0.5891 0.5866 [15] Ethylbenzene 0.8671 0.8668 [15] 0.8670 [12] 0.7767 0.7730 [16] 0.7800 [12] 0.6735 0.6763 [12] Cyclohexane [15] 0.679 63 [13] 0.5731 0.5702 [19] 0.5821 [15] 0.3895 0.3897 [15] Octane 0.6985 0.6982 [15] 0.698 62 [12] 0.7313 0.7226 [20] 0.7352 [15] 0.5108 0.5092 [15] Toluene 0.8620 0.8622 [15] 0.862 32 [21] 0.6413 0.6403 [15] 0.6421 [22] 0.5528 0.5521 [15] Ethylbenzene 0.8627 0.8625 [15] 0.8630 [23] 0.7323 0.7288 [24] 0.7367 [12] 0.6318 0.6354 [12] Cyclohexane 0.7739 0.7739 [15] 0.773 99 [21] 1.1540 1.1393 …”

Buoyancy-driven drop generation via microchannel revisited

“…Dimensionless numbers are usually used to represent the effect of various forces acting on the drop during (Chevalier et al 1990); C 16 (Awwad et al 1986 Weber number (We) shows the strength of kinetic force, the Bond number (Bo) represents the buoyancy force, and the Capillary number (Ca) accounts for the drag force, all against the interfacial tension force. Therefore, Eq.…”

A novel approach to predict the excess volume of hydrocarbon mixtures

“…Type of mixture Data sources A a n-Alkanes with n-alkanes Gomez-Ibanez and Liu (1963); Chevalier et al (1990); Somoza et al (1984); Garcia et al (1984); Blinowska and Brostow (1975); Jiangning and Asfour (1994); Garcia et al (1986); Hutchings and van Hook (1985); Wu and Asfour (1991) Cyclohexanes c with n-alkanes Awwad and Salman (1986a); Chevalier et al (1990); Somoza et al (1984); Garcia et al (1984); Aminabhavi et al (1996); Letcher and Spiteri (1979); Iloukhani and Rezaei-Sameti (2006); Letcher and Heyward (1983); ; Beg et al (1995) E d,e n-Cycloalkanes with n-alkanes Awwad and Salman (1986a); Chevalier et al (1990); Somoza et al (1984); Garcia et al (1984); Aminabhavi et al (1996); Letcher and Spiteri (1979); Letcher and Heyward (1983); Beg et al (1995); Martin and Symons (1981); Takigawa et al (2003) Remarks: (a) the data set also includes data of pentane-heptane and pentane-hexane up to 40 MPa; (b) benzene, ethylbenzene and methyl-substituted benzenes; (c) including methyl-and dimethyl-cyclohexane; (d) except for cyclopentane; (e) categories D and E have an overlap of 54 mixtures.…”

“…In a mixture of chain-like and plate-like or ring-like molecules holes can be formed that are larger than those that are formed in either of ; note that the datapoints occur once above and once below unity (data from Gomez-Ibanez and Liu, 1963;Chevalier et al, 1990;Somoza et al, 1984;Garcia et al, 1984;Blinowska and Brostow, 1975;Jiangning and Asfour, 1994;Garcia et al, 1986;Hutchings and van Hook, 1985;Hamam et al, 1984;Dingan et al, 1986;Pecar and Dolecek, 2003;Ewing and Marsh, 1974;Ewing et al, 1970). Awwad et al, 1986;Letcher et al, 1985;Awwad and Salman, 1986a;Chevalier et al, 1990;Somoza et al, 1984;Garcia et al, 1984;Caceres Alonso et al, 1986;Aminabhavi et al, 1996;Letcher and Spiteri, 1979;Letcher and Heyward, 1983;Beg et al, 1995;Martin and Symons, 1981;Takigawa et al, 2003;Spiteri and Letcher, 1979;Fujihara et al, 1985;Dohnal and Patterson, 1984). Remarks: (a) C5-C16 n-alkanes; (b) C7-C10 n-alkanes; (c) C6-C16 n-alkanes; (d) n-heptane with cis-and transdecalin.…”

“…Here too, there is a clear trend: the higher the total number of side groups is, the higher G W cyclohexane + n-alkane a cyclohexane + methylpentane cyclohexane + dimethylbutane methylcyclohexane + n-alkane a × dimethylcyclohexane + n-alkane b + trimethylcyclohexane + n-hexane 6. Effect of side groups on alkanes and cyclohexane on G W at 298.15 K and 1 atm (data from Awwad and Salman, 1986a;Chevalier et al, 1990;Somoza et al, 1984;Garcia et al, 1984;Aminabhavi et al, 1996;Letcher and Spiteri, 1979;Iloukhani and Rezaei-Sameti, 2006;Letcher and Heyward, 1983;Beg et al, 1995;Takigawa et al, 2003).…”