ACS Publications. Most Trusted. Most Cited. Most Read
My Activity
CONTENT TYPES

Figure 1Loading Img

Solubilities of Amide Compounds in Supercritical Carbon Dioxide

View Author Information
Key Laboratory of Analytical Chemistry of the State Ethnic Affairs Commission, College of Chemistry and Materials Science, South-Central University for Nationalities, Wuhan, 430074, P. R. China, and Beijing Key Laboratory of Printing & Packaging Material and Technology, Beijing Institute of Graphic Communication, Beijing 102600, P. R. China
* Corresponding author. Email: [email protected]
†South-Central University for Nationalities.
‡Beijing Institute of Graphic Communication.
Cite this: J. Chem. Eng. Data 2008, 53, 9, 2189–2192
Publication Date (Web):August 21, 2008
https://doi.org/10.1021/je800434j
Copyright © 2008 American Chemical Society

    Article Views

    366

    Altmetric

    -

    Citations

    LEARN ABOUT THESE METRICS
    Read OnlinePDF (109 KB)

    Abstract

    2,2′-Oxybis(N,N-diethylacetamide), 2,2′-oxybis(N,N-dibutylacetamide), and 2,2′-oxybis(N,N-dihexylacetamide) were synthesized, and their structures were confirmed by IR, NMR, and elemental analysis. The solubilities of compounds were measured at temperatures ranging from (313 to 333) K and pressures from (8.7 to 16.4) MPa in supercritical carbon dioxide. The measured solubilities were correlated using a semiempirical model. The calculated results showed satisfactory agreement with the experimental data and differed from the measured values by between (4.54 and 30.84) %.

    Cited By

    This article is cited by 24 publications.

    1. Zhao Tang, Jun-su Jin, Ze-ting Zhang, and Hong-tao Liu . New Experimental Data and Modeling of the Solubility of Compounds in Supercritical Carbon Dioxide. Industrial & Engineering Chemistry Research 2012, 51 (15) , 5515-5526. https://doi.org/10.1021/ie2016224
    2. Zhen Yang, Hai-Jian Yang, Jia Tian, Cun-Yue Guo, and Hakwon Kim . High Solubility and Partial Molar Volume of 2,2′-Oxybis(N,N-bis(2-methoxyethyl)acetamide) in Supercritical Carbon Dioxide. Journal of Chemical & Engineering Data 2011, 56 (4) , 1191-1196. https://doi.org/10.1021/je101104m
    3. Hai-Jian Yang, Jia Tian, and Hakwon Kim . New Highly CO2-Philic Diglycolic Acid Esters: Synthesis and Solubility in Supercritical Carbon Dioxide. Journal of Chemical & Engineering Data 2010, 55 (10) , 4130-4139. https://doi.org/10.1021/je900893e
    4. Hai-Jian Yang and Wei Wang. Solubility Comparison of Bis(2-hydroxyethyl) Ether and Tetraethylene Glycol before and after End-Group Modification by Ethyl Oxalyl Chloride in Supercritical Carbon Dioxide. Journal of Chemical & Engineering Data 2010, 55 (6) , 2279-2283. https://doi.org/10.1021/je900802d
    5. Wei Wang, Hai-Jian Yang, Juncheng Hu and Cun-Yue Guo . Solubilities of Diglycolic Acid Esters at Temperatures Ranging from (343 to 363) K in Supercritical Carbon Dioxide. Journal of Chemical & Engineering Data 2010, 55 (2) , 694-697. https://doi.org/10.1021/je900417c
    6. Fei Chang, Hakwon Kim and Yunja Kwon. Solubility of Novel CO2-Soluble Pyridine Derivatives in Supercritical Carbon Dioxide. Journal of Chemical & Engineering Data 2009, 54 (4) , 1262-1265. https://doi.org/10.1021/je800737d
    7. Yaoping Xie, Hai-Jian Yang, Wei Wang and Rong Chen . Solubilities of Diglycolic Acid Esters in Supercritical Carbon Dioxide. Journal of Chemical & Engineering Data 2009, 54 (1) , 102-107. https://doi.org/10.1021/je800683e
    8. A. Abdallah el hadj, M. Laidi, S. Hanini. AI-PCSAFT approach: New high predictive method for estimating PC-SAFT pure component properties and phase equilibria parameters. Fluid Phase Equilibria 2022, 555 , 113297. https://doi.org/10.1016/j.fluid.2021.113297
    9. N. A. Bondarenko, K. V. Tcarkova, S. K. Belus’, O. I. Artyushin, A. S. Peregudov. Novel Bis[N-alkyl-N-(2-diphenylphosphinylethyl)]diglycolamides: Synthesis and NMR Spectroscopy Studies. Russian Journal of General Chemistry 2021, 91 (2) , 181-189. https://doi.org/10.1134/S1070363221020055
    10. Noor U Din Reshi, Masood Ahmad Rizvi, Syed Kazim Moosvi, Mudasir Ahmad, Adil Gani. Solubility of organic compounds in scCO2. 2020, 379-411. https://doi.org/10.1016/B978-0-12-817388-6.00016-7
    11. Junsu Jin, Lintao Guo, Chengwei Chang, Hong Meng. Solubility of polystyrene with various molecular weights in subcritical 1,1,1,2‐tetrafluoroethane: experiment and modified model. Polymer International 2018, 67 (6) , 700-707. https://doi.org/10.1002/pi.5558
    12. Aicha Belghait, Cherif Si-Moussa, Maamar Laidi, Salah Hanini. Semi-empirical correlation of solid solute solubility in supercritical carbon dioxide: Comparative study and proposition of a novel density-based model. Comptes Rendus Chimie 2018, 21 (5) , 494-513. https://doi.org/10.1016/j.crci.2018.02.006
    13. Francesca Ingrosso, Manuel F. Ruiz‐López. Modeling Solvation in Supercritical CO 2. ChemPhysChem 2017, 18 (19) , 2560-2572. https://doi.org/10.1002/cphc.201700434
    14. Emilio San-Fabián, Francesca Ingrosso, Alexandrine Lambert, Margarita I. Bernal-Uruchurtu, Manuel F. Ruiz-López. Theoretical insights on electron donor–acceptor interactions involving carbon dioxide. Chemical Physics Letters 2014, 601 , 98-102. https://doi.org/10.1016/j.cplett.2014.03.084
    15. Piyong Zhang, Hai-Jian Yang, Lingxiao Xu. Solubilities and partial molar volumes of new CO2-philic propane derivatives in supercritical carbon dioxide. The Journal of Chemical Thermodynamics 2013, 67 , 234-240. https://doi.org/10.1016/j.jct.2013.08.015
    16. Zhuofu Cai, Lihua Wang, Hai-Jian Yang, Lu Zhao. Solubility of 2-methyl-2-propyl-1,3-propanediol and its derivatives in supercritical carbon dioxide: measurement and mathematical modeling. The Journal of Chemical Thermodynamics 2013, 66 , 71-79. https://doi.org/10.1016/j.jct.2013.06.015
    17. Luis Miguel Azofra, Muhannad Altarsha, Manuel F. Ruiz-López, Francesca Ingrosso. A theoretical investigation of the CO2-philicity of amides and carbamides. Theoretical Chemistry Accounts 2013, 132 (4) https://doi.org/10.1007/s00214-012-1326-4
    18. Ying Li, Zhao Tang, Junsu Jin, Zeting Zhang. Binary and ternary solubility of amino- and nitro-benzoic acids in supercritical carbon dioxide. Fluid Phase Equilibria 2013, 344 , 71-78. https://doi.org/10.1016/j.fluid.2013.01.021
    19. Lu Zhao, Hai-Jian Yang, Zhuofu Cai. Solubility comparison and partial molar volumes of 1,2-hexanediol before and after end-group modification by methyl oxalyl chloride and ethyl oxalyl monochloride in supercritical CO2. The Journal of Chemical Thermodynamics 2013, 57 , 46-53. https://doi.org/10.1016/j.jct.2012.08.020
    20. Jing Jin, Hai-Jian Yang, Ning Zhang, Fei Chang. Solubilities and partial molar volumes of 1-methypropanedioate derivatives in supercritical carbon dioxide. Fluid Phase Equilibria 2012, 334 , 43-50. https://doi.org/10.1016/j.fluid.2012.07.026
    21. Fei Chang, Jing Jin, Ning Zhang, Gang Wang, Hai-Jian Yang. The effect of the end group, molecular weight and size on the solubility of compounds in supercritical carbon dioxide. Fluid Phase Equilibria 2012, 317 , 36-42. https://doi.org/10.1016/j.fluid.2011.12.018
    22. José M.S. Fonseca, Ralf Dohrn, Stephanie Peper. High-pressure fluid-phase equilibria: Experimental methods and systems investigated (2005–2008). Fluid Phase Equilibria 2011, 300 (1-2) , 1-69. https://doi.org/10.1016/j.fluid.2010.09.017
    23. Jia Tian, Hai‐Jian Yang, Wei Wang, Hakwon Kim. Metal Ions Extraction from Solid Matrix in Supercritical Carbon Dioxide with DMBP as Chelating Ligand. CLEAN – Soil, Air, Water 2010, 38 (5-6) , 543-547. https://doi.org/10.1002/clen.201000106
    24. Hai‐Jian Yang, Hakwon Kim, Cun‐Yue Guo. Metal Ion Extraction with Bipyridine Derivatives as Chelating Ligands in Supercritical Carbon Dioxide. CLEAN – Soil, Air, Water 2010, 38 (2) , 159-166. https://doi.org/10.1002/clen.200900274

    Pair your accounts.

    Export articles to Mendeley

    Get article recommendations from ACS based on references in your Mendeley library.

    Pair your accounts.

    Export articles to Mendeley

    Get article recommendations from ACS based on references in your Mendeley library.

    You’ve supercharged your research process with ACS and Mendeley!

    STEP 1:
    Click to create an ACS ID

    Please note: If you switch to a different device, you may be asked to login again with only your ACS ID.

    Please note: If you switch to a different device, you may be asked to login again with only your ACS ID.

    Please note: If you switch to a different device, you may be asked to login again with only your ACS ID.

    MENDELEY PAIRING EXPIRED
    Your Mendeley pairing has expired. Please reconnect