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https://dspace.iiti.ac.in/handle/123456789/14504
Title: | Metal-Free Polydiacetylene-Functionalized Polymer for Photocatalytic Anionic and Cationic Dye Degradation and CO2 Capture |
Authors: | Dhruv, Likhi Agarwal, Sweta Das, Apurba Kumar |
Keywords: | CO2 capture;dye degradation;polydiacetylene;topochemical polymerization;water remediation |
Issue Date: | 2024 |
Publisher: | American Chemical Society |
Citation: | Dhruv, L., Agarwal, S., & Das, A. K. (2024). Metal-Free Polydiacetylene-Functionalized Polymer for Photocatalytic Anionic and Cationic Dye Degradation and CO2 Capture. ACS Applied Polymer Materials. Scopus. https://doi.org/10.1021/acsapm.4c01483 |
Abstract: | It is important to tackle sustainability challenges using affordable, metal-free porous organic polymers. Herein, we report the synthesis of a visible-light-responsive, metal-free polydiacetylene-based conjugated covalent organic polymer (COP). This is accomplished by photopolymerizing its diacetylene monomer (DA) without the need for a chemical reaction initiator or byproducts. The visible light response and porosity of the PDA@COP are utilized for the photocatalytic degradation of individual dyes (MO, anionic & MB, cationic) and their mixture, as well as for CO2 capture applications. When exposed to relatively low-power blue light (12 W), the PDA@COP demonstrates photocatalytic degradation of 98% for MB and 84% for MO, with rate constants of 0.021 and 0.010 min-1 over a period of 180 min, respectively. In contrast, a binary mixture of the dye solutions (MO + MB) shows a degradation of 99.9% for MB and 88% for MO, with rate constants of 0.042 and 0.017 min-1 in just 100 min, respectively, due to the synergetic interchange of O2•- and •OH radicals. Moreover, the PDA@COP demonstrates remarkable recyclability. Additionally, the PDA@COP shows a CO2 uptake of 66.72 cm3·g-1 (2.72 mmol·g-1), which is a 3.45 times increase compared to DA. © 2024 American Chemical Society. |
URI: | https://doi.org/10.1021/acsapm.4c01483 https://dspace.iiti.ac.in/handle/123456789/14504 |
ISSN: | 2637-6105 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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