Spectroscopic monitoring of polyurethane-based nanocomposite as a potential catalyst for the reduction of dyes.

Khalida Naseem, Qirrat Wakeel Manj, Saba Akram, Samreen Shabbir, Ayesha Noor, Zahoor H Farooqi, Saba Urooge Khan, Majid Ali, Muhammad Faizan Nazar, Sajjad Haider, Kamran Alam
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Abstract

In this study, AgNPs-loaded polyurethane-sodium alginate (PU-S/Alg) composite polymers were prepared by precipitation polymerization and in-situ reduction method. Their catalytic potential was evaluated for the reduction of methyl orange (MO), brilliant blue (BB), Rhodamine B (RhB), 4-nitroaniline (4-NA), and 4-nitrophenol (4-NP). Successful preparation of samples was confirmed by UV-Visible spectrophotometry (UV-Visible), Fourier transform infrared (FTIR), and Scanning electron microscopy (SEM) analysis. During the catalytic study, the value of kapp for the reduction of MO in the presence of NaBH4 and catalyst was found 0.488 min-1 while, in the presence of NaBH4 and catalyst alone, were found as 0.9 × 10-4 and 0.8 × 10-5 min-1, respectively which indicates the role of catalyst in making the reaction speedy. The value of kapp for the reduction of BB, RhB, 4-NA, and 4-NP was found as 0.764, 0.475, 0.212 and 0.757 min-1, respectively. Simultaneous reduction of dyes induced a decreased reaction completion time under the same reaction conditions. A slight increase in the value of kapp for the catalytic reduction of MO was also observed when reactions were performed in the presence of ionic media of different salts such as NaCl, KCl, CaCl2, and MnCl2. The rate of reduction of MO was increased with the increase in ionic strength of the medium. However, the presence of SDS (surfactant) in the reaction mixture induced the decreased activity of the catalyst and increased reaction completion time. The same value of kapp for the reduction of MO was observed in the case of freshly prepared and several days old nanocomposite catalyst. These results illustrate the stability and maintained catalytic potential of metal NPs for a prolonged time. Our reported catalyst also showed good potential for the treatment of dyes-polluted textile industry wastewater.

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聚氨酯基纳米复合材料作为染料还原潜在催化剂的光谱监测。
本研究采用沉淀聚合和原位还原法制备了载 AgNPs 的聚氨酯-海藻酸钠(PU-S/Alg)复合聚合物。评估了它们还原甲基橙(MO)、亮蓝(BB)、罗丹明 B(RhB)、4-硝基苯胺(4-NA)和 4-硝基苯酚(4-NP)的催化潜力。紫外-可见分光光度法(UV-Visible)、傅立叶变换红外光谱(Fourier transform infrared)和扫描电子显微镜(Scanning electron microscopy)分析证实了样品的成功制备。在催化研究过程中,发现在 NaBH4 和催化剂存在的情况下,还原 MO 的 kapp 值为 0.488 min-1,而在 NaBH4 和催化剂单独存在的情况下,kapp 值分别为 0.9 × 10-4 和 0.8 × 10-5 min-1,这表明催化剂在加快反应速度方面发挥了作用。还原 BB、RhB、4-NA 和 4-NP 的 kapp 值分别为 0.764、0.475、0.212 和 0.757 min-1。在相同的反应条件下,同时还原染料导致反应完成时间缩短。当反应在 NaCl、KCl、CaCl2 和 MnCl2 等不同盐类的离子介质中进行时,还观察到催化还原 MO 的 kapp 值略有增加。MO 的还原速率随着介质离子强度的增加而增加。然而,反应混合物中 SDS(表面活性剂)的存在导致催化剂活性降低,反应完成时间延长。在新制备的纳米复合催化剂和使用数天的纳米复合催化剂中,都观察到了相同的 MO 还原 kapp 值。这些结果说明了金属 NPs 的稳定性和长时间保持催化潜能的能力。我们报告的催化剂在处理受染料污染的纺织工业废水方面也表现出了良好的潜力。
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