Matveev Dmitry, Anokhina Tatyana, Raeva Alisa, Borisov Ilya, Grushevenko Evgenia, Khashirova Svetlana, Volkov Alexey, Bazhenov Stepan, Volkov Vladimir, Maksimov Anton
A.V.Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Leninsky Prospect, 29, 119991 Moscow, Russia.
Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory, 1, 119991 Moscow, Russia.
Polymers (Basel). 2024 Dec 10;16(24):3453. doi: 10.3390/polym16243453.
The scope of this work was to develop a thin-film composite (TFC) membrane for the separation of CO/CO mixtures, which are relevant for many processes of gas processing and gasification of carbon-based feedstock. Special attention was given to the development of highly permeable porous polysulfone (PSF) supports (more than 26,000 GPU for CO) since both the selective and support layers contribute significantly to the overall performance of the TFC membrane. The PSF porous support is widely used in commercial and lab-scale TFC membranes, and its porous structure and other exploitation parameters are set during the non-solvent-induced phase separation (NIPS) process. Since the casting solution properties (e.g., viscosity) and the interactions in a three-component system (polymer, solvent, and non-solvent) play noticeable roles in the NIPS process, polysulfone samples in a wide range of molecular weights (M = 76,000-122,000 g·mol) with terminal hydroxyl groups were synthesized for the first time. Commercial PSF with predominantly terminal chlorine groups (Ultrason S 6010) was used as a reference. The PSF samples were characterized by NMR, DSC, and TGA methods, and the Hansen solubility parameters were calculated. It was found that increasing the ratio of terminal -OH over -Cl groups improved the "solubility" of PSF in N-methyl-2-pyrrolidone (NMP) and water. A direct dependence of the gas permeance of porous supports on the coagulation rate of the casting solution was identified for the first time. It was shown that the use of synthesized PSF (M = 76,000 g·mol, M/M = 3.0, (-OH):(-Cl) ratio of 4.7:1) enabled a porous support with a CO permeance of 26,700 GPU to be obtained, while the support formed from a commercial PSF Ultrason S 6010 (M = 68,000 g·mol, M/M = 1.7, (-OH):(-Cl) ratio of 1:1.9) under the same conditions demonstrated 4300 GPU. The siloxane-based materials were used for the selective layer since the thin films based on rubbery polymers do not undergo the same accelerating physical aging as glassy polymers. Two types of materials were screened for the selective layer: synthesized polymethyltrifluoroethylacrylate siloxane-polydecylmethylsiloxane (50F3) copolymer, and polydimethylsiloxane (PDMS). 50F3 siloxane was studied for gas separation applications for the first time. It was shown that the permeance of composite membranes based on high-performance porous supports from the PSF samples synthesized was 3.5 times higher than that from similar composite membranes based on supports from a commercial Ultrason S 6010 PSF with a permeance value of 4300 GPU for CO. It was found that the enhanced gas permeance of composite membranes based on the highly permeable porous PSF supports developed was observed for both 50F3 polysiloxane and commercial PDMS. At the same time, the CO/CO selectivity of the composite membranes with a 50F3-selective layer (9.1-9.3) is 1.5 times higher than that of composite membranes with a PDMS-selective layer. This makes the F-containing 50F3 polysiloxane a promising polymer for CO/CO separation.
这项工作的范围是开发一种用于分离CO/CO混合物的薄膜复合(TFC)膜,这种混合物与许多碳基原料的气体处理和气化过程相关。由于选择性层和支撑层对TFC膜的整体性能都有显著贡献,因此特别关注高渗透性多孔聚砜(PSF)支撑体的开发(CO渗透率超过26,000 GPU)。PSF多孔支撑体广泛应用于商业和实验室规模的TFC膜中,其多孔结构和其他开发参数在非溶剂诱导相分离(NIPS)过程中设定。由于浇铸溶液的性质(如粘度)以及三元体系(聚合物、溶剂和非溶剂)中的相互作用在NIPS过程中起着显著作用,首次合成了一系列具有端羟基的不同分子量(M = 76,000 - 122,000 g·mol)的聚砜样品。以主要含有端氯基团的商业PSF(Ultrason S 6010)作为参考。通过NMR、DSC和TGA方法对PSF样品进行了表征,并计算了汉森溶解度参数。发现增加端 -OH与 -Cl基团的比例可提高PSF在N - 甲基 - 2 - 吡咯烷酮(NMP)和水中的“溶解度”。首次确定了多孔支撑体的气体渗透通量与浇铸溶液凝固速率之间的直接关系。结果表明,使用合成的PSF(M = 76,000 g·mol,M/M = 3.0,(-OH):(-Cl)比例为4.7:1)能够获得CO渗透通量为26,700 GPU的多孔支撑体,而在相同条件下由商业PSF Ultrason S 6010(M = 68,000 g·mol,M/M = 1.7,(-OH):(-Cl)比例为1:1.9)形成的支撑体的CO渗透通量为4300 GPU。基于橡胶态聚合物的薄膜不像玻璃态聚合物那样会经历相同的加速物理老化,因此将硅氧烷基材料用于选择性层。对选择性层筛选了两种材料:合成的聚甲基三氟乙基丙烯酸酯硅氧烷 - 聚癸基甲基硅氧烷(50F3)共聚物和聚二甲基硅氧烷(PDMS)。50F3硅氧烷首次用于气体分离应用研究。结果表明,基于合成的PSF样品的高性能多孔支撑体制备的复合膜的渗透通量比基于商业Ultrason S 6010 PSF支撑体(CO渗透通量值为4300 GPU)的类似复合膜高3.5倍。发现基于所开发的高渗透性多孔PSF支撑体制备的复合膜,对于50F3聚硅氧烷和商业PDMS都表现出增强的气体渗透通量。同时,具有50F3选择性层的复合膜的CO/CO选择性(9.1 - 9.3)比具有PDMS选择性层的复合膜高1.5倍。这使得含氟的50F3聚硅氧烷成为用于CO/CO分离的有前景的聚合物。