{"title":"Functionalized multi-walled carbon nanotube thin-layered hollow fiber membrane for enantioselective permeation of racemic β-substituted-α-amino acids","authors":"Monti Gogoi, Rajiv Goswami, Alimpia Borah, Chinmoy Bhuyan, Hrishikesh Sarmah, Swapnali Hazarika","doi":"10.1007/s12039-022-02076-8","DOIUrl":null,"url":null,"abstract":"<div><p>Utilization of carbon materials having excellent selectivity and robustness can have tremendous influence in the field of membrane-based separation. Herein, a hybrid polysulfone multi-walled carbon nanotube Hollow Fiber (HF) membrane was fabricated for enantioseparation of β-substituted-α-amino acids. Thin Film Nanocomposite (TFN) membrane was prepared <i>via</i> interfacial polymerization between D-tryptophan with carboxylated multi-walled carbon nanotubes and trimesoylchloride. The enantioseparation performance of the membranes was demonstrated through sorption and permeation study. On passing a racemate solution through the cross-linked membranes, the D-tryptophan-linked chiral probe adsorbed the D-isomer of the racemate, and L-isomer was passed to permeate side through the membrane. In a nutshell, the thin film nanocomposite enacts as the effective layer over the HF membrane which ensured that the apportioned chiral selectors were adequate to attain 99% of enantioselectivity.</p><h3>Graphical abstract</h3><p>Hybrid nanocomposite membranes were prepared <i>via</i> interfacial polymerization between D- tryptophan with carboxylated multi-walled carbon nanotubes and trimesoyl chloride over polysulfone support. On passing a racemate solution of β-substituted-α-amino acids through the hybrid membranes, the chiral probe selectively adsorbed the D-isomer. The thin-film nanocomposite enacts as the effective layer over the hollow fiber membrane which ensures the apportioned chiral selectors were adequate to attain 99% of enantioselectivity.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":50242,"journal":{"name":"Journal of Chemical Sciences","volume":"134 3","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2022-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-022-02076-8","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 6
Abstract
Utilization of carbon materials having excellent selectivity and robustness can have tremendous influence in the field of membrane-based separation. Herein, a hybrid polysulfone multi-walled carbon nanotube Hollow Fiber (HF) membrane was fabricated for enantioseparation of β-substituted-α-amino acids. Thin Film Nanocomposite (TFN) membrane was prepared via interfacial polymerization between D-tryptophan with carboxylated multi-walled carbon nanotubes and trimesoylchloride. The enantioseparation performance of the membranes was demonstrated through sorption and permeation study. On passing a racemate solution through the cross-linked membranes, the D-tryptophan-linked chiral probe adsorbed the D-isomer of the racemate, and L-isomer was passed to permeate side through the membrane. In a nutshell, the thin film nanocomposite enacts as the effective layer over the HF membrane which ensured that the apportioned chiral selectors were adequate to attain 99% of enantioselectivity.
Graphical abstract
Hybrid nanocomposite membranes were prepared via interfacial polymerization between D- tryptophan with carboxylated multi-walled carbon nanotubes and trimesoyl chloride over polysulfone support. On passing a racemate solution of β-substituted-α-amino acids through the hybrid membranes, the chiral probe selectively adsorbed the D-isomer. The thin-film nanocomposite enacts as the effective layer over the hollow fiber membrane which ensures the apportioned chiral selectors were adequate to attain 99% of enantioselectivity.
期刊介绍:
Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.