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ЖУРНАЛЫ // Теплофизика высоких температур

ТВТ, 2005, том 43, выпуск 6, страницы 855–859 (Mi tvt1458)

Растворимость салициловой кислоты в сверхкритическом диоксиде углерода
Р. Н. Максудов, А. Е. Новиков, А. Н. Сабирзянов, Ф. М. Гумеров

Эта публикация цитируется в следующих статьяx:
  1. Surya Chandra Tiwari, Sreedevi Upadhyayula, Advances and Technology Development in Greenhouse Gases: Emission, Capture and Conversion., 2024, 227  crossref
  2. E. E. Sergeev, Yu. A. Rodikova, E. G. Zhizhina, “Salicylic Acid Synthesis Methods: A Review”, Catal. Ind., 16:3 (2024), 312  crossref
  3. E. E. Sergeev, Yu. A. Rodikova, E. G. Zhizhina, “Methods for the synthesis of salicylic acid. A review”, Kat.v.prom., 23:6 (2023), 52  crossref
  4. R. F. Gabitov, V. F. Khairutdinov, F. M. Gumerov, Z. I. Zaripov, T. R. Bilalov, Jean-Marie Kuagu, F. R. Gabitov, S. V. Mazanov, V. A. Petrov, V. K. Mingazova, “Some Thermodynamic Properties of Propiconazole Used as Fungicide and its Mixture with Carbon Dioxide Involved in the Process of Wood Impregnation”, J Eng Phys Thermophy, 96:2 (2023), 520  crossref
  5. Omid Faraz, Mozhdeh Poustchi, Ebrahim Nazari Denyani, Parsa Movahedi, Fereshteh Rajabi Kouchi, Reza Shahriari, “Thermodynamic modeling of pharmaceuticals solubility in pure, mixed and supercritical solvents”, Journal of Molecular Liquids, 353 (2022), 118809  crossref
  6. Wang Sh.-W., Chen J.-Z., Hsieh Ch.-M., “Measurement and Correlation of Solubility of Methylsalicylic Acid Isomers in Supercritical Carbon Dioxide”, J. Chem. Eng. Data, 66:1 (2021), 280–289  crossref  isi  scopus
  7. Gurina D.L., Antipova M.L., Odintsova E.G., Petrenko V.E., “Solvation of Hydroxybenzoic and Hydroxycinnamic Acids in Supercritical Carbon Dioxide: Formation of Hydrogen Bonds With a Polar Cosolvent”, Russ. J. Phys. Chem. B, 12:8 (2018), 1276–1286  crossref  isi  scopus
  8. Antipova M.L., Gurina D.L., Odintsova E.G., Petrenko V.E., “Formation of Solvate Structures By the Ortho-, Meta-, and Para-Isomers of Hydroxybenzoic Acid in Supercritical Fluid”, Russ. J. Phys. Chem. A, 91:4 (2017), 708–714  crossref  isi  scopus
  9. Valentina E. Petrenko, Marina L. Antipova, Darya L. Gurina, “Salicylic acid, acetylsalicylic acid, methyl salicylate, salicylamide, and sodium salicylate in supercritical carbon dioxide: Solute – cosolvent hydrogen bonds formation”, The Journal of Supercritical Fluids, 116 (2016), 62  crossref
  10. Jing Zhu, Yubo Wang, Chengwei Chang, Hailun Wang, Junsu Jin, “Determination and modelling of solubility of o -aminobenzamide and its mixture with o -nitrobenzoic acid in supercritical carbon dioxide”, Journal of CO2 Utilization, 14 (2016), 83  crossref
  11. Petrenko V.E., Antipova M.L., Gurina D.L., “Solvation of Salicylic Acid in Pure, Methanol-Modified and Water-Modified Supercritical Carbon Dioxide: Molecular Dynamics Simulation”, J. Supercrit. Fluids, 104 (2015), 227–233  crossref  isi
  12. Antipova M.L., Gurina D.L., Odintsova E.G., Petrenko V.E., “Solvation of O-Hydroxybenzoic Acid in Pure and Modified Supercritical Carbon Dioxide, According To Numerical Modeling Data”, Russ. J. Phys. Chem. A, 89:8 (2015), 1381–1388  crossref  isi  elib
  13. Petrenko V.E., Antipova M.L., Gurina D.L., Odintsova E.G., “Formation of Molecular Complexes of Salicylic Acid, Acetylsalicylic Acid, and Methyl Salicylate in a Mixture of Supercritical Carbon Dioxide With a Polar Cosolvent”, Russ. J. Phys. Chem. A, 89:8 (2015), 1389–1395  crossref  isi  elib
  14. Antipova M.L., Gurina D.L., Petrenko V.E., “Hydrogen-Bonded Clusters and Solvate Structures in the Supercritical Co2-Water-O-Hydroxybenzoic Acid System: the Car-Parrinello Molecular Dynamics”, Russ. J. Phys. Chem. A, 88:2 (2014), 259–266  crossref  isi  elib
  15. Valentina E. Petrenko, Marina L. Antipova, Darya L. Gurina, “The structure of hydrated complexes of o-hydroxybenzoic acid in water-modified supercritical carbon dioxide: The Car-Parrinello molecular dynamics simulation”, The Journal of Supercritical Fluids, 85 (2014), 1  crossref
  16. Berkant Kayan, Yu Yang, Edward J. Lindquist, A. Murat Gizir, “Solubility of Benzoic and Salicylic Acids in Subcritical Water at Temperatures Ranging from (298 to 473) K”, J. Chem. Eng. Data, 55:6 (2010), 2229  crossref


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