화학공학소재연구정보센터
Journal of Industrial and Engineering Chemistry, Vol.77, 344-354, September, 2019
Greener processes in the preparation of thin film nanocomposite membranes with diverse metal-organic frameworks for organic solvent nanofiltration
E-mail:
The toxic solvent dimethylformamide has been replaced by the greener dimethylsulfoxide in the casting and activation processes for the preparation of thin film composite (TFC) membranes. This methodology has been validated with the use of MOFs ZIF-8, ZIF-93 and UiO-66 as fillers for thin-film nanocomposite (TFN) membranes. These membranes were successfully applied in the organic solvent nanofiltration of sunset yellow (SY) in methanol obtaining the highest permeance when UiO-66 and ZIF-93 were used with a value of 11 L m-2 h-1 bar-1. The permeance improvements are related to the MOF porosity, polyamide-MOF layer thickness and the hydrophilic/hydrophobic character of the membrane.
  1. Marchetti P, Solomon MFJ, Szekely G, Livingston AG, Chem. Rev., 114(21), 10735 (2014)
  2. Radjenovic J, Petrovic M, Ventura F, Barcelo D, Water Res., 42, 3601 (2008)
  3. Kosutic K, Furac L, Sipos L, Kunst B, Sep. Purif. Technol., 42(2), 137 (2005)
  4. Tang C, Chen V, Desalination, 143(1), 11 (2002)
  5. Buonomenna MG, Bae J, Sep. Purif. Rev., 44, 157 (2015)
  6. Petersen RJ, J. Membr. Sci., 83, 81 (1993)
  7. Jeong BH, Hoek EMV, Yan YS, Subramani A, Huang XF, Hurwitz G, Ghosh AK, Jawor A, J. Membr. Sci., 294(1-2), 1 (2007)
  8. Lau WJ, Gray S, Matsuura T, Emadzadeh D, Chen JP, Ismail AF, Water Res., 80, 306 (2015)
  9. Emadzadeh D, Lau WJ, Matsuura T, Rahbari-Sisakht M, Ismail AF, Chem. Eng. J., 237, 70 (2014)
  10. Soroko I, Livingston A, J. Membr. Sci., 343(1-2), 189 (2009)
  11. Peyravi M, Jahanshahi M, Rahimpour A, Javadi A, Hajavi S, Chem. Eng. J., 241, 155 (2014)
  12. Yin J, Kim ES, Yang J, Deng BL, J. Membr. Sci., 423, 238 (2012)
  13. Yin J, Zhu GC, Deng BL, Desalination, 379, 93 (2016)
  14. Sorribas S, Gorgojo P, Tellez C, Coronas J, Livingston AG, J. Am. Chem. Soc., 135(40), 15201 (2013)
  15. Duan JT, Pan YC, Pacheco F, Litwiller E, Lai ZP, Pinnau I, J. Membr. Sci., 476, 303 (2015)
  16. Echaide-Gorriz C, Sorribas S, Tellez C, Coronas J, RSC Adv., 6, 90417 (2016)
  17. Wang H, Zeng Z, Xu P, Li L, Zeng G, Xiao R, Tang Z, Huang D, Tang L, Lai C, Jiang D, Liu Y, Yi H, Qin L, Ye S, Ren X, Tang W, Chem. Soc. Rev., 48, 488 (2019)
  18. Jiang D, Xu P, Wang H, Zeng G, Huang D, Chen M, Lai C, Zhang C, Wan J, Xue W, Coord. Chem. Rev., 376, 449 (2018)
  19. Xiong W, Zeng Z, Li X, Zeng G, Xiao R, Yang Z, Zhou Y, Zhang C, Cheng M, Hu L, Zhou C, Qin L, Xu R, Zhang Y, Chemosphere, 120, 1061 (2018)
  20. Guillen GR, Pan YJ, Li MH, Hoek EMV, Ind. Eng. Chem. Res., 50(7), 3798 (2011)
  21. Echaide-Gorriz C, Navarro M, Tellez C, Coronas J, Dalton Trans., 46, 6244 (2017)
  22. Solomon MFJ, Bhole Y, Livingston AG, J. Membr. Sci., 423, 371 (2012)
  23. United States Environmental Protection Agency, https://www.epa.gov/green-chemistry, (accessed 16 June 2018).
  24. Anastas PT, Kirchhoff MM, Accounts Chem. Res., 35, 686 (2002)
  25. Prat D, Pardigon O, Flemming HW, Letestu S, Ducandas VR, Isnard P, Guntrum E, Senac T, Ruisseau S, Cruciani P, Org. Process Res. Dev., 17, 1517 (2013)
  26. European Chemicals Agency, https://echa.europa.eu/candidate-list-table,(accessed 16 June 2018).
  27. Burgal JD, Peeva L, Livingston A, Green Chem., 18, 2374 (2016)
  28. Hua D, Japip S, Wang KY, Chung TS, ACS Sustain. Chem. Eng., 6, 10696 (2018)
  29. Figoli A, Marino T, Simone S, Di Nicolo E, Li XM, He T, Tornaghi S, Drioli E, Green Chem., 16, 4034 (2014)
  30. Soroko I, Bhole Y, Livingston AG, Green Chem., 13, 162 (2011)
  31. Capello C, Fischer U, Hungerbuhler K, Green Chem., 9, 927 (2007)
  32. Valenzano L, Civalleri B, Chavan S, Bordiga S, Nilsen MH, Jakobsen S, Lillerud KP, Lamberti C, Chem. Mater., 23, 1700 (2011)
  33. Morris W, He N, Ray KG, Klonowski P, Furukawa H, Daniels IN, Houndonougbo YA, Asta M, Yaghi OM, Laird BB, J. Phys. Chem. C, 116, 24084 (2012)
  34. Park KS, Ni Z, Cote AP, Choi JY, Huang RD, Uribe-Romo FJ, Chae HK, O’Keeffe M, Yaghi OM, Proc. Natl. Acad. Sci. U. S. A., 103, 10186 (2006)
  35. Liu X, Li Y, Ban Y, Peng Y, Jin H, Bux H, Xu L, Caro J, Yang W, Chem. Commun., 49, 9140 (2013)
  36. Liedana N, Galve A, Rubio C, Tellez C, Coronas J, ACS Appl. Mater. Interfaces, 4, 5016 (2012)
  37. Hou L, Wang L, Zhang N, Xie Z, Dong D, Polym. Chem., 7, 5828 (2016)
  38. Yang Q, Wiersum AD, Jobic H, Guillerm V, Serre C, Llewellyn PL, Maurin G, J. Phys. Chem. C, 115, 13768 (2011)
  39. Sorribas S, Zornoza B, Tellez C, Coronas J, Chem. Commun., 48, 9388 (2012)
  40. Cavka JH, Jakobsen S, Olsbye U, Guillou N, Lamberti C, Bordiga S, Lillerud KP, J. Am. Chem. Soc., 130(42), 13850 (2008)
  41. Chavan S, Vitillo JG, Gianolio D, Zavorotynska O, Civalleri B, Jakobsen S, Nilsen MH, Valenzano L, Lamberti C, Lillerud KP, Bordiga S, Phys. Chem. Chem. Phys., 14, 1614 (2012)
  42. Gupta KM, Qiao Z, Zhang K, Jiang J, ACS Appl. Mater. Interfaces, 8, 13392 (2016)
  43. Gorgojo P, Jimenez-Solomon MF, Livingston AG, Desalination, 344, 181 (2014)
  44. Sanchez-Lainez J, Paseta L, Navarro M, Zornoza B, Tellez C, Coronas J, Adv. Mater. Interfaces, 5, 180064 (2018)
  45. Ghosh AK, Jeong BH, Huang XF, Hoek EMV, J. Membr. Sci., 311(1-2), 34 (2008)
  46. Paseta L, Potier G, Abbott S, Coronas J, Org. Biomol. Chem., 13, 1724 (2015)
  47. Hansen CM, Prog. Org. Coat., 51, 77 (2004)
  48. Koo CH, Mohammad AW, Suja' F, Talib MZM, Desalination, 287, 167 (2012)
  49. Guo XY, Liu DH, Han TT, Huang HL, Yang QY, Zhong CL, AIChE J., 63(4), 1303 (2017)
  50. Roy S, Ntim SA, Mitra S, Sirkar KK, J. Membr. Sci., 375(1-2), 81 (2011)
  51. Shao L, Cheng XQ, Wang ZX, Ma J, Guo ZH, J. Membr. Sci., 452, 82 (2014)
  52. Li YF, Mao H, Zhang HQ, Yang GH, Ding R, Wang JT, Sep. Purif. Technol., 165, 60 (2016)
  53. Darvishmanesh S, Buekenhoudt A, Degreve J, Van der Bruggen B, J. Membr. Sci., 334(1-2), 43 (2009)
  54. Darvishmanesh S, Degreve J, Van der Bruggen B, ChemphysChem, 11, 404 (2010)