2020-Thermally rearranged polymer membranes containing highly rigid biphenyl ortho-hydroxyl diamine for hydrogen separation
作者:XiaofanHu Won Hee Lee Jiayi Zhaob Ju Sung Kim ZhenWang Jingling Yan Yongbing Zhuang Young Moo Leea
关键字:Thermally rearranged polymer membranes
论文来源:期刊
具体来源:Journal of Membrane Science
发表时间:2020年
A novel bulky and rigid ortho-hydroxyl diamine,
3,3′-diamino-5,5′,6,6′-tetramethyl-[1,1′-biphenyl]-2,2′-diol (TMBDA),
was synthesized for gas separation membranes in this study. The chemical
structure of TMBDA with four methyl groups and a fixed twist biphenyl
center was rationally designed, and consequently presented a superior
energy barrier of rotation, which efficiently suppressed chain motion
and enhanced polymer rigidity. Four types of TMBDA-based polyimides
(PIs) were prepared with two commercially available dianhydrides, i.e.,
4,4''''-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) and
pyromellitic dianhydride (PMDA), from two different synthetic routes,
azeotropic and chemical imidization. Thermally rearranged (TR) polymers
were obtained from TMBDA-based PIs by thermal treatment at various
temperatures. Thermal properties and physicochemical characteristics of
TMBDA-based PIs and TR polymers were investigated. The resulting
polymers exhibited high glass transition temperatures (Tg) and contorted backbone structures with three discrete d-spacing values, where the smallest interchain d-spacing was located between the kinetic diameters of H2 and CH4 molecules. Moreover, TMBDA-based TR polymers showed outstanding performances in hydrogen separation with comparable H2 permeability and higher selectivity than reported TRs. For instance, 6F-TM-Ac-425 exhibited a H2 permeability of 325 Barrer with H2/CH4 and H2/N2 selectivities of 50 and 39, respectively, approaching to the 2008 Robeson upper bound.