journal article·2014-10-22

Silylated Mesoporous Silica Membranes on Polymeric Hollow Fiber Supports: Synthesis and Permeation Properties

Hyung-Ju Kim, Nicholas A. Brunelli, Andrew J. Brown, Kwang-Suk Jang, Wun-gwi Kim, Fereshteh Rashidi, Justin R. Johnson, William J. Koros, Christopher W. Jones, Sankar Nair

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Abstract

We report the synthesis and organic/water separation properties of mesoporous silica membranes, supported on low-cost and scalable polymeric (polyamide-imide) hollow fibers, and modified by trimethylsilylation with hexamethyldisilazane. Thin (∼1 μm) defect-free membranes are prepared, with high room-temperature gas permeances (e.g., 20,000 GPU for N2). The membrane morphology is characterized by multiple techniques, including SEM, TEM, XRD, and FT-ATR spectroscopy. Silylation leads to capping of the surface silanol groups in the mesopores with trimethylsilyl groups, and does not affect the integrity of the mesoporous silica structure and the underlying hollow fiber. The silylated membranes are evaluated for pervaporative separation of ethanol (EtOH), methylethyl ketone (MEK), ethyl acetate (EA), iso-butanol (i-BuOH), and n-butanol (n-BuOH) from their dilute (5 wt %) aqueous solutions. The membranes show separation factors in the range of 4-90 and high organic fluxes in the range of 0.18-2.15 kg m(-2) h(-1) at 303 K. The intrinsic selectivities (organic/water permeability ratios) of the silylated membranes at 303 K are 0.33 (EtOH/water), 0.5 (MEK/water), 0.25 (EA/water), 1.25 (i-BuOH/water), and 1.67 (n-BuOH/water) respectively, in comparison to 0.05, 0.015, 0.005, 0.08, and 0.14 for the unmodified membranes. The silylated membranes allow upgradation of water/organics feeds to permeate streams with considerably higher organics content. The selective and high-flux separation is attributed to both the organophilic nature of the modified mesopores and the large effective pore size. Comparison with other organics/water separation membranes reveals that the present membranes show promise due to high flux, use of scalable and low-cost supports, and good separation factors that can be further enhanced by tailoring the mesopore silylation chemistry.
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Research context

OpenAlex topics: Membrane Separation and Gas Transport · Zeolite Catalysis and Synthesis · Covalent Organic Framework Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive, Atlanta, Georgia 30332-0100, United States

School of Chemistry and Biochemistry, Georgia Institute of Technology, 901 Atlantic Drive, Atlanta, Georgia 30332-0400, United States

Funding

Phillips 66 Company

References (67)

Show source-provided references
1. Bernardo P. · Ind. Eng. Chem. Res. · 2009 · 48 · 463810.1021/ie8019032 ↗
2. Striemer C. C. · Nature · 2007 · 445 · 74910.1038/nature05532 ↗
3. Vankelecom I. F. J. · Chem. Rev. · 2002 · 102 · 377910.1021/cr0103468 ↗
4. Strathmann H. · AIChE J. · 2001 · 47 · 107710.1002/aic.690470514 ↗
5. Robeson L. M. · J. Membr. Sci. · 1991 · 62 · 16510.1016/0376-7388(91)80060-J ↗
6. Robeson L. M. · J. Membr. Sci. · 2008 · 320 · 39010.1016/j.memsci.2008.04.030 ↗
7. Gonzalez-Marcos J. A. · J. Appl. Polym. Sci. · 2004 · 94 · 139510.1002/app.21029 ↗
8. Jian K. · J. Membr. Sci. · 1996 · 117 · 11710.1016/0376-7388(96)00065-8 ↗
9. Karlsson H. O. E. · J. Membr. Sci. · 1993 · 76 · 12110.1016/0376-7388(93)85211-E ↗
10. Williams M. E. · Ind. Eng. Chem. Res. · 1999 · 38 · 368310.1021/ie990140l ↗
11. Hartono S. B. · Langmuir · 2009 · 25 · 641310.1021/la900023p ↗
12. Sen T. · J. Am. Chem. Soc. · 2006 · 128 · 713010.1021/ja061393q ↗
13. Zhang L. · Adv. Funct. Mater. · 2008 · 18 · 320310.1002/adfm.200800363 ↗
14. Kittur A. A. · J. Membr. Sci. · 2005 · 247 · 7510.1016/j.memsci.2004.09.010 ↗
15. Xu Q. · J. Membr. Sci. · 2012 · 415 · 43510.1016/j.memsci.2012.05.031 ↗
16. Choi J. · Science · 2009 · 325 · 59010.1126/science.1176095 ↗
17. Ge Q. Q. · J. Am. Chem. Soc. · 2009 · 131 · 1705610.1021/ja9082057 ↗
18. Kanezashi M. · AIChE J. · 2008 · 54 · 147810.1002/aic.11457 ↗
19. Xu L. · Anal. Chem. · 2007 · 79 · 524110.1021/ac070449b ↗
20. Yoo W. C. · Angew. Chem., Int. Ed. · 2010 · 49 · 869910.1002/anie.201004029 ↗
21. Huang Y. · Ind. Eng. Chem. Res. · 2010 · 49 · 376010.1021/ie901545r ↗
22. Vane L. M. · J. Chem. Technol. Biotechnol. · 2010 · 85 · 50210.1002/jctb.2318 ↗
23. Vane L. M. · J. Membr. Sci. · 2010 · 364 · 10210.1016/j.memsci.2010.08.006 ↗
24. Dacosta A. R. · Ind. Eng. Chem. Res. · 1994 · 33 · 184510.1021/ie00031a026 ↗
25. Jang K. S. · Chem. Mater. · 2011 · 23 · 302510.1021/cm200939d ↗
26. Hicks J. C. · Langmuir · 2006 · 22 · 267610.1021/la053024y ↗
27. Hodgkins R. P. · Langmuir · 2007 · 23 · 883810.1021/la063395u ↗
28. Melero J. A. · Chem. Rev. · 2006 · 106 · 379010.1021/cr050994h ↗
29. Wight A. P. · Chem. Rev. · 2002 · 102 · 358910.1021/cr010334m ↗
30. Chaikittisilp W. · Energy Fuels · 2011 · 25 · 552810.1021/ef201224v ↗
31. Chaikittisilp W. · Chem. Mater. · 2013 · 25 · 61310.1021/cm303931q ↗
32. Chew T. L. · Adv. Colloid Interface Sci. · 2010 · 153 · 4310.1016/j.cis.2009.12.001 ↗
33. Kumar P. · Microporous Mesoporous Mater. · 2008 · 110 · 59510.1016/j.micromeso.2007.06.040 ↗
34. Nishiyama N. · J. Membr. Sci. · 2001 · 182 · 23510.1016/S0376-7388(00)00570-6 ↗
35. Pedernera M. · J. Membr. Sci. · 2009 · 326 · 13710.1016/j.memsci.2008.09.050 ↗
36. Sakamoto Y. · Microporous Mesoporous Mater. · 2007 · 101 · 30310.1016/j.micromeso.2006.11.007 ↗
37. Lu S. F. · Adv. Mater. · 2010 · 22 · 97110.1002/adma.200903091 ↗
38. McKeen J. C. · Chem. Mater. · 2008 · 20 · 512210.1021/cm801418r ↗
39. Park S. J. · J. Membr. Sci. · 2010 · 357 · 110.1016/j.memsci.2010.04.011 ↗
40. Seshadri S. K. · Microporous Mesoporous Mater. · 2010 · 129 · 22810.1016/j.micromeso.2009.09.020 ↗
41. Kumar P. · Ind. Eng. Chem. Res. · 2008 · 47 · 20110.1021/ie070700d ↗
42. Park D. H. · Microporous Mesoporous Mater. · 2003 · 66 · 6910.1016/j.micromeso.2003.08.025 ↗
43. Kim H. J. · J. Membr. Sci. · 2013 · 427 · 29310.1016/j.memsci.2012.10.012 ↗
44. Brown A. J. · Angew. Chem., Int. Ed. · 2012 · 51 · 1061510.1002/anie.201206640 ↗
45. Belwalkar A. · J. Membr. Sci. · 2008 · 319 · 19210.1016/j.memsci.2008.03.044 ↗
46. Collins T. J. · Biotechniques · 2007 · 43 · 2510.2144/000112517 ↗
47. Al-Juaied M. · J. Membr. Sci. · 2006 · 274 · 22710.1016/j.memsci.2005.08.013 ↗
48. Vu D. Q. · Ind. Eng. Chem. Res. · 2002 · 41 · 36710.1021/ie010119w ↗
49. Baker R. W. · J. Membr. Sci. · 2010 · 348 · 34610.1016/j.memsci.2009.11.022 ↗
50. Beaurecard G. P. · J. Appl. Polym. Sci. · 2001 · 79 · 226410.1002/1097-4628(20010321)79:12<2264::AID-APP1034>3.0.CO;2-E ↗
51. Bhatia S. K. · Langmuir · 2010 · 26 · 837310.1021/la9047962 ↗
52. Bhatia S. K. · Chem. Eng. Sci. · 2011 · 66 · 28410.1016/j.ces.2010.10.038 ↗
53. Wu S. F. · J. Membr. Sci. · 2012 · 390 · 175
54. Baker R. W. · J. Membr. Sci. · 2010 · 348 · 34610.1016/j.memsci.2009.11.022 ↗
55. Schoutens G. H. · Process Biochem. · 1985 · 20 · 117
56. Li L. · J. Membr. Sci. · 2004 · 243 · 17710.1016/j.memsci.2004.06.015 ↗
57. Thiyagarajan R. · Desalination · 2011 · 277 · 17810.1016/j.desal.2011.04.020 ↗
58. Zhan X. · Appl. Biochem. Biotechnol. · 2010 · 160 · 63210.1007/s12010-008-8510-y ↗
59. Zhang Q. G. · RSC Adv. · 2013 · 3 · 185510.1039/C2RA21827E ↗
60. Tian X. Z. · J. Hazard. Mater. · 2008 · 153 · 12810.1016/j.jhazmat.2007.08.029 ↗
61. Shu X. J. · Ind. Eng. Chem. Res. · 2012 · 51 · 1207310.1021/ie301087u ↗
62. Tuan V. A. · Chem. Commun. · 2001 · 6 · 58310.1039/b008547m ↗
63. Sakaki K. · Desalin. Water Treat. · 2011 · 34 · 29010.5004/dwt.2011.2855 ↗
64. Negishi H. · Chem. Lett. · 2010 · 39 · 131210.1246/cl.2010.1312 ↗
65. Chen X. S. · Desalination · 2008 · 234 · 28610.1016/j.desal.2007.09.096 ↗
66. Zhou H. L. · Sep. Purif. Technol. · 2011 · 79 · 37510.1016/j.seppur.2011.03.026 ↗
67. Liu X. L. · J. Membr. Sci. · 2011 · 369 · 22810.1016/j.memsci.2010.11.074 ↗