Affiliation: | 1. Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, Shaoxing University, Zhejiang Province, People's Republic of China
Contribution: ?Investigation (lead);2. Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, Shaoxing University, Zhejiang Province, People's Republic of China
Contribution: ?Investigation (equal);3. Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, Shaoxing University, Zhejiang Province, People's Republic of China;4. Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, Shaoxing University, Zhejiang Province, People's Republic of China
Contribution: Data curation (equal);5. Department of Textile, Zhejiang Industry Polytechnic College, Zhejiang Province, People's Republic of China;6. School of Pharmacy, Jiamusi University, Jiamusi, Heilongjiang, People's Republic of China
Contribution: ?Investigation (supporting);7. Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, Shaoxing University, Zhejiang Province, People's Republic of China
School of Pharmacy, Jiamusi University, Jiamusi, Heilongjiang, People's Republic of China
Contribution: Funding acquisition (lead) |
Abstract: | Pd/C embedded polystyrene fibers were successfully prepared by electrospinning. The polystyrene molecules were then cross-linked by paraformaldehyde in sulfuric acid to improve the solvent resistance of composite fibers. SEM images conformed the preparation of uniform and smooth composite fibers. FT-IR spectra demonstrated that the polystyrene molecules inside fibers have been sulphonated and crosslinked. Heck reactions were used to evaluate the catalytic performance of these novel composite fibers. The catalysis results show that this composite fiber mat catalyzed Heck reactions could be evidently promoted by using preferred reducing alcohol agent and solvent. Under the optimized reaction conditions, this composite fiber mat could effectively catalyze the Heck reactions of aromatic iodides with n-butyl acrylate to afford the products with satisfied yields. Especially, compared with the particulate Pd/C catalyst, the separation and recycling of this fibrous catalyst from the reaction mixture were significantly improved due to the larger fibrous structure. At last, this fiber catalyst was successfully reused for eight times with little loss of initial catalytic activity, which was even better than the pristine Pd/C catalyst. Hence, embedment of particulate supported metal catalysts inside the crosslinked polystyrene fibers can effectively improve their catalytic performance and handiness. |