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Bubble Temperature Measurements on Binary Mixtures Formed by Cyclohexane at 94.7 kPa

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Properties Group, Chemical Engineering Laboratory, Indian Institute of Chemical Technology, Hyderabad 500 007, India; Regional Engineering College, Durgapur 713 203, India; Institute of Technology, Banaras Hindu University, Varanasi 635 751, India; and Chaitanya Bharati Institute of Technology, Hyderabad 500 075, India
Cite this: J. Chem. Eng. Data 2003, 48, 2, 351–353
Publication Date (Web):January 14, 2003
https://doi.org/10.1021/je020148t
Copyright © 2003 American Chemical Society

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    Abstract

    Bubble temperatures at 94.7 k Pa, over the entire composition range, are measured for eight binary mixtures formed by cyclohexane with 1,1,1-trichloroethane, 1,1,2,2-tetrachloroethane, epichlorohydrin, 1,2-dimethoxyethane, 1,4-dioxane, 2-picoline, N,N-dimethylformamide, and dimethylacetamide. A Swietoslawski-type ebulliometer was used for the measurements. The liquid-phase mole fraction versus temperature measurements were represented by the Wilson model.

     Indian Institute of Chemical Technology.

     Regional Engineering College.

    §

     Banaras Hindu University.

     Chaitanya Bharati Institute of Technology.

    *

     Author for correspondence. E-mail: [email protected].

    Cited By

    This article is cited by 10 publications.

    1. Wanliang Mi, Ruixin Tong, Chao Hua, Kai Yue, Debiao Jia, Ping Lu, and Fang Bai . Vapor–Liquid Equilibrium Data for Binary Systems of N,N-Dimethylacetamide with Cyclohexene, Cyclohexane, and Benzene Separately at Atmospheric Pressure. Journal of Chemical & Engineering Data 2015, 60 (11) , 3063-3068. https://doi.org/10.1021/acs.jced.5b00011
    2. Beatriz Marrufo, Margarita Sanchotello, Sonia Loras. Isobaric vapor–liquid equilibria for binary and ternary mixtures with cyclohexane, cyclohexene, and morpholine at 100kPa. Fluid Phase Equilibria 2010, 296 (2) , 178-183. https://doi.org/10.1016/j.fluid.2010.04.008
    3. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. (Chloromethyl)oxirane <undefined optical isomer> C3H5ClO + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_2496
    4. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. 2-Methylpyridine C6H7N + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_2604
    5. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. Morpholine C4H9NO + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_2909
    6. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. N,N-Dimethylmethanamide C3H7NO + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_2915
    7. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. 1,1,1-Trichloroethane C2H3Cl3 + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_473
    8. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. 1,1,2,2-Tetrachloroethane C2H2Cl4 + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_475
    9. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. 2,5-Dioxahexane C4H10O2 + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_803
    10. I. Wichterle, J. Linek, Z. Wagner, J.-C. Fontaine, K. Sosnkowska-Kehiaian, H. V. Kehiaian. 1,4-Dioxane C4H8O2 + C6H12 Cyclohexane. , 1-1. https://doi.org/10.1007/978-3-540-49315-0_856

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