Polyamide Nanofilms through a Non-Isothermal-Controlled Interfacial Polymerization

Research output: Contribution to journalArticleResearch

Authors

  • Guang Jin Zhao
  • Lu Lu Li
  • Hai Qi Gao
  • Zhi Jian Zhao
  • Zi Fan Pang
  • Chun Lei Pei
  • Zhou Qu
  • Liang Liang Dong
  • De Wei Rao
  • Jürgen Caro
  • Hong Meng

External Research Organisations

  • Beijing University of Chemical Technology
  • Xinjiang University
  • Jiangnan University
  • Jiangsu University of Science and Technology
  • Tianjin University
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Details

Original languageEnglish
Article number2313026
JournalAdvanced functional materials
Volume34
Issue number18
Early online date20 Jan 2024
Publication statusPublished - 2 May 2024

Abstract

Efficient thin film composite polyamide (PA) membranes require optimization of interfacial polymerization (IP) process. However, it is challengeable owing to its ultrafast reaction rate coupled with mass and heat transfer, yielding heterogeneous PA membranes with low performance. Herein, a non-isothermal-controlled IP (NIIP) method is proposed to fabricate a highly permeable and selective PA membrane by engineering IP at the cryogenic aqueous phase (CAP) to achieve synchronous control of heat and mass transfer in the interfacial region. The CAP also enables the phase transition of the aqueous solution from the liquid to solid state, providing a more comprehensive understanding of the fundamental mechanisms involved in different phase states in the IP process. Consequently, the PA membrane exhibits excellent separation performance with ultrahigh water permeance (42.9 L m−2 h−1 bar−1) and antibiotic desalination efficiency (antibiotic/NaCl selectivity of 159.3). This study provides new insights for the in-depth understanding of the precise mechanism linking IP to the performance of the targeting membrane.

Keywords

    antibiotic desalination, interfacial polymerization, membrane separation, nanofiltration, polyamide

ASJC Scopus subject areas

Cite this

Polyamide Nanofilms through a Non-Isothermal-Controlled Interfacial Polymerization. / Zhao, Guang Jin; Li, Lu Lu; Gao, Hai Qi et al.
In: Advanced functional materials, Vol. 34, No. 18, 2313026, 02.05.2024.

Research output: Contribution to journalArticleResearch

Zhao, GJ, Li, LL, Gao, HQ, Zhao, ZJ, Pang, ZF, Pei, CL, Qu, Z, Dong, LL, Rao, DW, Caro, J & Meng, H 2024, 'Polyamide Nanofilms through a Non-Isothermal-Controlled Interfacial Polymerization', Advanced functional materials, vol. 34, no. 18, 2313026. https://doi.org/10.1002/adfm.202313026
Zhao, G. J., Li, L. L., Gao, H. Q., Zhao, Z. J., Pang, Z. F., Pei, C. L., Qu, Z., Dong, L. L., Rao, D. W., Caro, J., & Meng, H. (2024). Polyamide Nanofilms through a Non-Isothermal-Controlled Interfacial Polymerization. Advanced functional materials, 34(18), Article 2313026. https://doi.org/10.1002/adfm.202313026
Zhao GJ, Li LL, Gao HQ, Zhao ZJ, Pang ZF, Pei CL et al. Polyamide Nanofilms through a Non-Isothermal-Controlled Interfacial Polymerization. Advanced functional materials. 2024 May 2;34(18):2313026. Epub 2024 Jan 20. doi: 10.1002/adfm.202313026
Zhao, Guang Jin ; Li, Lu Lu ; Gao, Hai Qi et al. / Polyamide Nanofilms through a Non-Isothermal-Controlled Interfacial Polymerization. In: Advanced functional materials. 2024 ; Vol. 34, No. 18.
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abstract = "Efficient thin film composite polyamide (PA) membranes require optimization of interfacial polymerization (IP) process. However, it is challengeable owing to its ultrafast reaction rate coupled with mass and heat transfer, yielding heterogeneous PA membranes with low performance. Herein, a non-isothermal-controlled IP (NIIP) method is proposed to fabricate a highly permeable and selective PA membrane by engineering IP at the cryogenic aqueous phase (CAP) to achieve synchronous control of heat and mass transfer in the interfacial region. The CAP also enables the phase transition of the aqueous solution from the liquid to solid state, providing a more comprehensive understanding of the fundamental mechanisms involved in different phase states in the IP process. Consequently, the PA membrane exhibits excellent separation performance with ultrahigh water permeance (42.9 L m−2 h−1 bar−1) and antibiotic desalination efficiency (antibiotic/NaCl selectivity of 159.3). This study provides new insights for the in-depth understanding of the precise mechanism linking IP to the performance of the targeting membrane.",
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T1 - Polyamide Nanofilms through a Non-Isothermal-Controlled Interfacial Polymerization

AU - Zhao, Guang Jin

AU - Li, Lu Lu

AU - Gao, Hai Qi

AU - Zhao, Zhi Jian

AU - Pang, Zi Fan

AU - Pei, Chun Lei

AU - Qu, Zhou

AU - Dong, Liang Liang

AU - Rao, De Wei

AU - Caro, Jürgen

AU - Meng, Hong

N1 - Funding Information: This work was financially supported by the National Key Research and Development Program of China (2022YFB3804802) and National Natural Science Foundation of China (No. 22278178) and the Fundamental Research Funds for the Central Universities (JUSRP622035).

PY - 2024/5/2

Y1 - 2024/5/2

N2 - Efficient thin film composite polyamide (PA) membranes require optimization of interfacial polymerization (IP) process. However, it is challengeable owing to its ultrafast reaction rate coupled with mass and heat transfer, yielding heterogeneous PA membranes with low performance. Herein, a non-isothermal-controlled IP (NIIP) method is proposed to fabricate a highly permeable and selective PA membrane by engineering IP at the cryogenic aqueous phase (CAP) to achieve synchronous control of heat and mass transfer in the interfacial region. The CAP also enables the phase transition of the aqueous solution from the liquid to solid state, providing a more comprehensive understanding of the fundamental mechanisms involved in different phase states in the IP process. Consequently, the PA membrane exhibits excellent separation performance with ultrahigh water permeance (42.9 L m−2 h−1 bar−1) and antibiotic desalination efficiency (antibiotic/NaCl selectivity of 159.3). This study provides new insights for the in-depth understanding of the precise mechanism linking IP to the performance of the targeting membrane.

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