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一种用于降解硝基酚的高效银纳米颗粒固定化海藻酸钠-g-聚丙烯腈杂化光催化剂。

A Highly Efficient Ag Nanoparticle-Immobilized Alginate-g-Polyacrylonitrile Hybrid Photocatalyst for the Degradation of Nitrophenols.

作者信息

Hasan Imran, Shekhar Charu, Alharbi Walaa, Abu Khanjer Maymonah, Khan Rais Ahmad, Alsalme Ali

机构信息

Environmental Research Laboratory, Department of Chemistry, Chandigarh University, Gharuan, Mohali 140301, Punjab, India.

Department of Chemistry, Faculty of Science, King Khalid University, P.O. Box-9004, Abha 62529, Saudi Arabia.

出版信息

Polymers (Basel). 2020 Dec 19;12(12):3049. doi: 10.3390/polym12123049.

Abstract

Herein, we report PAN-g-Alg@Ag-based nanocatalysts synthesis via in situ oxidative free-radical polymerization of acrylonitrile (AN) using Alg@Ag nanoparticles (Alg@Ag NPs). Various analytical techniques, including FTIR, XRD, SEM, TEM, UV-Vis, and DSC, were employed to determine bonding interactions and chemical characteristics of the nanocatalyst. The optimized response surface methodology coupled central composite design (RSM-CCD) reaction conditions were a 35-min irradiation time in a 70-mg L 2,4-dinitrophenol (DNP) solution at pH of 4.68. Here, DNP degradation was 99.46% at a desirability of 1.00. The pseudo-first-order rate constant () values were 0.047, 0.050, 0.054, 0.056, 0.059, and 0.064 min with associated half-life () values of 14.74, 13.86, 12.84, 12.38, 11.74, 10.82, and 10.04 min that corresponded to DNP concentrations of 10, 20, 30, 40, 50, 60, and 70 mg L, respectively, in the presence of PAN-g-Alg@Ag (0.03 g). The results indicate that the reaction followed the pseudo-first-order kinetic model with an R value of 0.99. The combined absorption properties of PAN and Alg@Ag NPs on copolymerization on the surface contributed more charge density to surface plasmon resonance (SPR) in a way to degrade more and more molecules of DNP together with preventing the recombination of electron and hole pairs within the photocatalytic process.

摘要

在此,我们报道了通过使用Alg@Ag纳米颗粒(Alg@Ag NPs)对丙烯腈(AN)进行原位氧化自由基聚合来合成基于PAN-g-Alg@Ag的纳米催化剂。采用了各种分析技术,包括傅里叶变换红外光谱(FTIR)、X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外可见光谱(UV-Vis)和差示扫描量热法(DSC)来确定纳米催化剂的键合相互作用和化学特性。优化后的响应面方法结合中心复合设计(RSM-CCD)反应条件为:在pH值为4.68的70 mg/L 2,4-二硝基苯酚(DNP)溶液中照射35分钟。在此条件下,DNP降解率为99.46%,可取性为1.00。在存在0.03 g PAN-g-Alg@Ag的情况下,伪一级速率常数()值分别为0.047、0.050、0.054、0.056、0.059和0.064 min,相关的半衰期()值分别为14.74、13.86、12.84、12.38、11.74、10.82和10.04 min,分别对应DNP浓度为10、20、30、40、50、60和70 mg/L。结果表明,该反应遵循伪一级动力学模型,R值为0.99。PAN和Alg@Ag NPs在表面共聚时的联合吸收特性以一种方式为表面等离子体共振(SPR)贡献了更多的电荷密度,从而在光催化过程中降解越来越多的DNP分子,并防止电子和空穴对的复合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec17/7766039/24314e65d259/polymers-12-03049-g001.jpg

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