Your browser doesn't support javascript.
loading
Isoporous Membranes by the Symmetric Triblock Copolymer: A Strategy to Improve the Mechanical Strength without Sharply Changing the Pore Size and Permselectivity.
Wu, Tao; Wang, Zixiong; Yin, Fengjie; Wang, Wenjing; Yi, Zhuan.
Afiliación
  • Wu T; Center for Membrane and Water Science & Technology, Zhejiang University of Technology, Hangzhou 310014, China.
  • Wang Z; Huzhou Institute of Collaborative Innovation Center for Membrane Separation and Water treatment, Hong Feng Road, Huzhou 313000, China.
  • Yin F; Center for Membrane and Water Science & Technology, Zhejiang University of Technology, Hangzhou 310014, China.
  • Wang W; Center for Membrane and Water Science & Technology, Zhejiang University of Technology, Hangzhou 310014, China.
  • Yi Z; Center for Membrane and Water Science & Technology, Zhejiang University of Technology, Hangzhou 310014, China.
ACS Appl Mater Interfaces ; 16(28): 37073-37086, 2024 Jul 17.
Article en En | MEDLINE | ID: mdl-38958638
ABSTRACT
Isoporous membranes produced from diblock copolymers commonly display a poor mechanical property that shows many negative impacts on their separation application. It is theoretically predicted that dense films produced from symmetric triblock copolymers show much stronger mechanical properties than those of homologous diblock copolymers. However, to the best of our knowledge, symmetric triblock copolymers have rarely been fabricated into isoporous membranes before, and a full understanding of separation as well as mechanical properties of membranes prepared from triblock copolymers and homologous diblock copolymers has not been conducted, either. In this work, a cleavable symmetric triblock copolymer with polystyrene as the side block and poly(4-vinylpyridine) (P4VP) as the middle block was synthesized and designed by the RAFT polymerization using the symmetric chain transfer agent, which located at the center of polymer chains and could be removed to produce homologous diblock copolymers with half-length while having the same composition as that found in triblock copolymers. The self-assembly of these two copolymers in thin films and casting solutions was first investigated, observing that they displayed similar self-organized structures under these two conditions. When fabricated into isoporous membranes, they showed similar pore sizes (5-7% difference) and comparable rejection performance (∼10% difference). However, isoporous membranes produced from triblock copolymers showed significantly improved mechanical strength and higher toughness (2-10 times larger) as evidenced by the compacting resistance, strain-stress determination, and nanoindentation testing, suggesting the unique and novel structure-performance relationship in the isoporous membranes produced from symmetric triblock copolymers. The above finding will guide the way to fabricate mechanically robust isoporous membranes without notably changing the separation performance from rarely used symmetric triblock copolymers, which can be synthesized by the controlled polymerization as facilely as that found for diblock copolymers.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: China