Adewole J. K. :Membrane Separation of CO2 from Natural Gas

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RESEARCH POSTER PRESENTATION DESIGN © 2012 www.PosterPresentations.com Natural gas (NG) processing and membrane technology are two very important fields that are of great significance due to increasing demand for energy as well as gas mixtures separation. While NG is projected to be the number one primary source of energy by 2050, membrane separation is a commercially successful competitor to other separation techniques for energy efficient gas purification processes (Qiu et al., 2011). Most of the NG produced in the world is coproduced with acid gases such as CO 2 which need to be removed to increase the caloric value of NG. A comprehensive review of research efforts in CO 2 separation from natural gas is required to capture details of the current scientific and technological progresses on the development of new membrane materials with tailored gas transport properties, and the improvement of properties of the existing ones. This paper presents the progresses that have been achieved in the area of material science and engineering to eliminate the limitations that dominate the large scale application of membrane materials at the present time. Research efforts in material development in the context of the break through and challenges that exist for major industrial applications of membrane in CO 2 removal from NG are reported. Abstract Challenges in Membrane Materials Development for Gas Separation CO 2 -induced Plasticization and Conditioning Figure 4. Permeability of CO 2 as a function of Feed Pressure in Glassy PSF and Rubbery PEO (Data used were obtained from Scholes et al., (2010); and Lin and Freeman (2004)). Membrane with Higher Plasticization Pressure Figure 5. Separation Performance of Decarboxylation-induced Thermal Crosslinking of Hollow Fiber 6FDA-DAM:DABA (3:2) Membrane for Pure CO2 Gas (Data were obtained from Qiu et al., 2011) References Figure 6. (a) Separation Performance of Decarboxylation-induced Thermal Crosslinking of Hollow Fiber 6FDA-DAM:DABA (3:2) Membrane for 50%CO 2 /50% CH 4 Gas using data from Qiu et al. (2011) (b)Improved Plasticization Resistance via Crosslinking of 6FDA-DAM-DABA (2:1) using data from Staudt-Bickel & Koros (1999); and Kratochvil & Koros (2008) The three important identified challenges are: 1.Better gas selectivity without sacrificing gas permeability 2.Problem of CO2-induced plasticization and conditioning 3.Maintaining the long-term gas separation performance by overcoming the problems of physical aging Askari, M., Xiao, Y., Li, P., & Chung, T.-S. (2012 ). Natural gas purification and olefin/paraffin separation using cross-linkable 6FDA-Durene/DABA co-polyimides grafted with α,β and γ cyclodextrin. Journal of Membrane Science , 390– 391 , 141– 151. Bernardo, P., Drioli, E., & Golemme, G. (2009). Membrane Gas Separation: A Review/State of the Art. Ind. Eng. Chem. Res. , 48, 4638–4663. Han, S. H., Lee, J. E., Lee, K.-J., Park, H. B., & Lee, Y. M. (2010). Highly gas permeable and microporous polybenzimidazole membrane by thermal rearrangement. Journal of Membrane Science , 357 , 143–151. Kratochvil, A. M., & Koros, W. J. (2008). Decarboxylation-Induced Cross-Linking of a Polyimide for Enhanced CO2 Plasticization Resystance. Macromolecules , 41, 7920- 7927. Lin, H., & Freeman, B. (2004 ). Gas solubility, diffusivity and permeability in poly(ethylene oxide). Journal of Membrane Science , 239 , 105–117. Park, H. B., Han, S. H., Jung, C. H., Lee, Y. M., & Hill, A. J. (2010). Thermally rearranged (TR) polymer membranes for CO2 separation. Journal of Membrane Science , 359 , 11–24. Qiu, W., Chen, C.-C., Xu, L., Cui, L., Paul, D. R., & Koros, W. (2011). Sub-Tg Cross-Linking of a Polyimide Membrane for Enhanced CO2 Plasticization Resistance for Natural Gas Separation. Macromolecules , 44, 6046–6056. Scholes, C. A., Chen, G. Q., Stevens, G., & Kentish, S. E. (2010). Plasticization of ultra- thin polysulfone membranes by carbon dioxide. Journal of Membrane Science , 346 , 208–214. Staudt-Bickel, C., & Koros, W. J. (1999). Improvement of CO2/CH4 separation characteristics of polyimides by chemical crosslinking. Journal of Membrane Science , 155, 145–154. Wind, J. D., Paul, D. R., & Koros, W. J. (2004 ). Natural gas permeation in polyimide membranes. Journal of Membrane Science , 228 , 227–236. Xiao, Y., Low, B. T., Hosseini, S. S., Chung, T. S., & Paul, D. R. (2009 ). The strategies of molecular architecture and modi cation of polyimide-based membranes for CO2 removal from natural gas - A review. Progress in Polymer Science , 34 , 561–580 Figure 3. Thermally Rearranged Polymer Membranes that Surpassed the 2008 Upper Bound [(a) Han et al., (2010) (b) Park et al. (2010)] Figure 2. Robeson’s 1991 and 2008 Upper Bound Curves Representing a General Trade-Off for Membrane Gas Separation Performance [(a) Wind et al., (2004); (b) Xiao et al., (2009)] Figure 1. Permeability and Permselectivity of gases at feed pressure of 3.5 bar; membrane thickness of 20 μm (Bernardo et al., 2009) 180oC, 24hr 330oC, 20hr 350oC, 1hr 130 250 265 27 27 26 55 69 69 Separation Perform anceofDecarboxylation-induced Therm al Permeability PermSelectivity Plasticization Pressure (barrer) (bar) Better Balance of Selectivity and Permeability School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang, Malaysia Jimoh K. Adewole and Abdul Latif Ahmad Membrane Separation of CO 2 from Natural Gas: A State-of-the-Art Review on Material Development 0 100 200 300 400 500 600 Cellulose Accetae Cytop HyflonA D 60 HyflonAD 80 Teflon AF 1600 Perm eability(barrer) 0 5 10 15 20 25 30 35 40 45 50 Cellulose Accetae Cytop H yflonAD 60 HyflonAD 80 TeflonAF 1600 Perm selectivity (a) 120oC , 24hr 180oC , 24hr 300oC , 20hr 330oC , 20hr 350oC , 1hr 370oC , 1hr 150 140 190 290 330 450 14 45 48 48 48 48 Separation Perform anceofD ecarboxylation-induced T herm al Perm eability (B arrer) Plasticization Pressure (B ar) 0 10 20 30 40 50 60 Crosslinked w ith Ethyleneglycolin DMAc D ecarboxylation at highTem perature +220oC , 23hr D ecarboxylation at high Tem perature +220oC , 23hr+ rapid Q uenching from above Tg Plasticization Pressure (bar) Im proved A ntiplasticization R esistance via C rosslinking of 0 2 4 6 8 10 12 14 16 18 20 7 7.5 8 8.5 9 9.5 10 0 2 4 6 8 10 12 14 16 P erm eability in P E O (B arrer) P erm eab ility in P S F (B arrer) Feed Pressure (atm ) Polysulfone (PSF) Polyethylene oxide (PEO ) Perm eability of CO 2 as a function ofFeed Pressure in G lassy PSF and R ubbery PEO (Scholes etal.,2010;and Lin and Freem an,2004) M inim um P erm eability Plasticization Pressure (b) (a) (b) Department of Chemical Engineering, King Fahd University of Petroleum & Minerals, Dhahran 31261, Saudi Arabia DSL333

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Presentation at the 8 DSL Conference in Turkey, 2012

Transcript of Adewole J. K. :Membrane Separation of CO2 from Natural Gas

Page 1: Adewole J. K. :Membrane Separation of CO2 from Natural Gas

RESEARCH POSTER PRESENTATION DESIGN © 2012

www.PosterPresentations.com

Natural gas (NG) processing and membrane technology are two very important fields that are of great significance due to increasing demand for energy as well as gas mixtures separation. While NG is projected to be the number one primary source of energy by 2050, membrane separation is a commercially successful competitor to other separation techniques for energy efficient gas purification processes (Qiu et al., 2011). Most of the NG produced in the world is coproduced with acid gases such as CO2 which need to be removed to increase the caloric value of NG. A comprehensive review of research efforts in CO2 separation from natural gas is required to capture details of the current scientific and technological progresses on the development of new membrane materials with tailored gas transport properties, and the improvement of properties of the existing ones. This paper presents the progresses that have been achieved in the area of material science and engineering to eliminate the limitations that dominate the large scale application of membrane materials at the present time. Research efforts in material development in the context of the break through and challenges that exist for major industrial applications of membrane in CO2 removal from NG are reported.

Abstract

Challenges in Membrane Materials Development for Gas Separation

CO2-induced Plasticization and Conditioning

Figure 4. Permeability of CO2 as a function of Feed Pressure in Glassy PSF and Rubbery PEO (Data used were obtained from Scholes et al., (2010); and Lin and Freeman (2004)).

Membrane with Higher Plasticization Pressure

Figure 5. Separation Performance of Decarboxylation-induced Thermal Crosslinking of Hollow Fiber 6FDA-DAM:DABA (3:2) Membrane for Pure CO2 Gas (Data were obtained from Qiu et al., 2011)

References

Figure 6. (a) Separation Performance of Decarboxylation-induced Thermal Crosslinking of Hollow Fiber 6FDA-DAM:DABA (3:2) Membrane for 50%CO2 /50% CH4 Gas using data from Qiu et al. (2011) (b)Improved Plasticization Resistance via Crosslinking of 6FDA-DAM-DABA (2:1) using data from Staudt-Bickel & Koros (1999); and Kratochvil & Koros (2008)

The three important identified challenges are:

1.Better gas selectivity without sacrificing gas permeability

2.Problem of CO2-induced plasticization and conditioning

3.Maintaining the long-term gas separation performance by overcoming the problems of physical aging

Askari, M., Xiao, Y., Li, P., & Chung, T.-S. (2012 ). Natural gas purification and olefin/paraffin separation using cross-linkable 6FDA-Durene/DABA co-polyimides grafted with α,β and γ cyclodextrin. Journal of Membrane Science , 390– 391 , 141– 151.

Bernardo, P., Drioli, E., & Golemme, G. (2009). Membrane Gas Separation: A Review/State of the Art. Ind. Eng. Chem. Res. , 48, 4638–4663.

Han, S. H., Lee, J. E., Lee, K.-J., Park, H. B., & Lee, Y. M. (2010). Highly gas permeable and microporous polybenzimidazole membrane by thermal rearrangement. Journal of Membrane Science , 357 , 143–151.

Kratochvil, A. M., & Koros, W. J. (2008). Decarboxylation-Induced Cross-Linking of a Polyimide for Enhanced CO2 Plasticization Resystance. Macromolecules , 41, 7920- 7927.

Lin, H., & Freeman, B. (2004 ). Gas solubility, diffusivity and permeability in poly(ethylene oxide). Journal of Membrane Science , 239 , 105–117.

Park, H. B., Han, S. H., Jung, C. H., Lee, Y. M., & Hill, A. J. (2010). Thermally rearranged (TR) polymer membranes for CO2 separation. Journal of Membrane Science , 359 , 11–24.

Qiu, W., Chen, C.-C., Xu, L., Cui, L., Paul, D. R., & Koros, W. (2011). Sub-Tg Cross-Linking of a Polyimide Membrane for Enhanced CO2 Plasticization Resistance for Natural Gas Separation. Macromolecules , 44, 6046–6056.

Scholes, C. A., Chen, G. Q., Stevens, G., & Kentish, S. E. (2010). Plasticization of ultra-thin polysulfone membranes by carbon dioxide. Journal of Membrane Science , 346 , 208–214.

Staudt-Bickel, C., & Koros, W. J. (1999). Improvement of CO2/CH4 separation characteristics of polyimides by chemical crosslinking. Journal of Membrane Science , 155, 145–154.

Wind, J. D., Paul, D. R., & Koros, W. J. (2004 ). Natural gas permeation in polyimide membranes. Journal of Membrane Science , 228 , 227–236.

Xiao, Y., Low, B. T., Hosseini, S. S., Chung, T. S., & Paul, D. R. (2009 ). The strategies of molecular architecture and modification of polyimide-based membranes for CO2 removal from natural gas - A review. Progress in Polymer Science , 34 , 561–580

Figure 3. Thermally Rearranged Polymer Membranes that Surpassed the 2008 Upper Bound [(a) Han et al., (2010) (b) Park et al. (2010)]

Figure 2. Robeson’s 1991 and 2008 Upper Bound Curves Representing a General Trade-Off for Membrane Gas Separation Performance

[(a) Wind et al., (2004); (b) Xiao et al., (2009)]

Figure 1. Permeability and Permselectivity of gases at feed pressure of 3.5 bar; membrane thickness of 20 μm (Bernardo et al., 2009)

180oC, 24hr 330oC, 20hr 350oC, 1hr

130

250 265

27 27 2655 69 69

Separation Performance of Decarboxylation-induced Thermal Crosslinking of Hollow Fiber 6FDA-DAM:DABA (3:2) Membrane for

50%CO2 /50% CH4Gas (Qiu et al., 2011)

Permeability PermSelectivity Plasticization Pressure(barrer) (bar)

Better Balance of Selectivity and Permeability

School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang, Malaysia

Jimoh K. Adewole and Abdul Latif Ahmad

Membrane Separation of CO2 from Natural Gas:

A State-of-the-Art Review on Material Development

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Cellulose Accetae

Cytop Hyflon AD 60

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Permeability of Commercial Membranes

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Cellulose Accetae

Cytop Hyflon AD 60

Hyflon AD 80

Teflon AF 1600

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Permselectivity of Commercial Membranes

(a)

120oC, 24hr 180oC, 24hr 300oC, 20hr 330oC, 20hr 350oC, 1hr 370oC, 1hr

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1445 48 48 48 48

Separation Performance of Decarboxylation-induced Thermal Crosslinking of Hollow Fiber 6FDA-DAM:DABA (3:2) Membrane for

Pure CO2 Gas (Qiu et al., 2011)

Permeability (Barrer) Plasticization Pressure (Bar)

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Crosslinked with Ethylene glycol in

DMAc

Decarboxylation at high Temperature

+220 oC, 23hr

Decarboxylation at high Temperature+220 oC, 23hr + rapid Quenching from above Tg

Pla

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izat

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Pre

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Improved Antiplasticization Resistance via Crosslinking of 6FDA-DAM-DABA (2:1) (Staudt-Bickel & Koros ,1999; and

Kratochvil & Koros, 2008)

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Feed Pressure (atm)

Polysulfone (PSF) Polyethylene oxide (PEO)

Permeability of CO2 as a function of Feed Pressure in Glassy PSF and Rubbery PEO (Scholes et al., 2010; and Lin and Freeman, 2004)

Minimum Permeability

Plasticization Pressure

(b)

(a) (b)

Department of Chemical Engineering, King Fahd University of Petroleum & Minerals, Dhahran 31261, Saudi Arabia DSL333