负载金纳米颗粒的碳纳米管(Au-CNTs)作为对硝基苯酚还原高效催化剂的优化制备

F. Zulkifli, A. M. Md Jani, H. Yazid
{"title":"负载金纳米颗粒的碳纳米管(Au-CNTs)作为对硝基苯酚还原高效催化剂的优化制备","authors":"F. Zulkifli, A. M. Md Jani, H. Yazid","doi":"10.2174/2211544710666210608150209","DOIUrl":null,"url":null,"abstract":"\n\n The current work aims to enhance the catalytic performance of gold nanopar-ticle–carbon nanotube (Au-CNT) composites towards the reduction of p-nitrophenol.\n\n\n\n\n The synthesis of Au-CNT has received extensive attention because of their high stability and catalytic efficiency, particularly as a heterogeneous catalyst in the reduction of p-nitrophenol (p-NP) to p-aminophenol (p-AP) However, most of the Au-CNT preparation processes reported in the literature are time-consuming or require expensive instrumentation. In the present work, Au-CNT catalysts were synthesized via a straightforward, low-cost deposition–precipitation (DP) method.\n\n\n\n\n The aim of the study was to evaluate the effect of pH and aging time on catalytic activity of Au-CNTs catalyst.\n\n\n\n\n The Au-CNT nanocomposite catalysts were synthesized using a simple deposition–precipitation method and characterized by Brunauer–Emmett–Teller analysis, fourier transform infrared spectroscopy, atomic absorption spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy, and trans-mission electron microscopy.\n\n\n\n\nThe particle size and the loading of Au nanoparticles on the CNTs can be easily controlled by varying the pH and aging time during the synthesis process. The nanocomposite catalysts exhibited excellent catalytic activity for the reduction of p-nitrophenol to p-aminophenol in the presence of excess sodium borohydride (NaBH4). The highest rate constant (k) achieved based on the pseudo-first-order kinetic model was 1.2 × 10-3 s-1.\n\n\n\n\nThis study offers a simple and cost-effective route to synthesize Au-CNT catalysts with high stability and catalytic efficiency for large-scale applica-tions.\n\n","PeriodicalId":10862,"journal":{"name":"Current Catalysis","volume":"40 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Optimized Preparation of Gold Nanoparticles-loaded Carbon Nanotubes (Au-CNTs) as an Efficient Catalyst for p-Nitrophenol Reduction\",\"authors\":\"F. Zulkifli, A. M. Md Jani, H. Yazid\",\"doi\":\"10.2174/2211544710666210608150209\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\n The current work aims to enhance the catalytic performance of gold nanopar-ticle–carbon nanotube (Au-CNT) composites towards the reduction of p-nitrophenol.\\n\\n\\n\\n\\n The synthesis of Au-CNT has received extensive attention because of their high stability and catalytic efficiency, particularly as a heterogeneous catalyst in the reduction of p-nitrophenol (p-NP) to p-aminophenol (p-AP) However, most of the Au-CNT preparation processes reported in the literature are time-consuming or require expensive instrumentation. In the present work, Au-CNT catalysts were synthesized via a straightforward, low-cost deposition–precipitation (DP) method.\\n\\n\\n\\n\\n The aim of the study was to evaluate the effect of pH and aging time on catalytic activity of Au-CNTs catalyst.\\n\\n\\n\\n\\n The Au-CNT nanocomposite catalysts were synthesized using a simple deposition–precipitation method and characterized by Brunauer–Emmett–Teller analysis, fourier transform infrared spectroscopy, atomic absorption spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy, and trans-mission electron microscopy.\\n\\n\\n\\n\\nThe particle size and the loading of Au nanoparticles on the CNTs can be easily controlled by varying the pH and aging time during the synthesis process. The nanocomposite catalysts exhibited excellent catalytic activity for the reduction of p-nitrophenol to p-aminophenol in the presence of excess sodium borohydride (NaBH4). The highest rate constant (k) achieved based on the pseudo-first-order kinetic model was 1.2 × 10-3 s-1.\\n\\n\\n\\n\\nThis study offers a simple and cost-effective route to synthesize Au-CNT catalysts with high stability and catalytic efficiency for large-scale applica-tions.\\n\\n\",\"PeriodicalId\":10862,\"journal\":{\"name\":\"Current Catalysis\",\"volume\":\"40 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-06-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2211544710666210608150209\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2211544710666210608150209","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

本研究旨在提高金纳米颗粒-碳纳米管(Au-CNT)复合材料对对硝基苯酚还原的催化性能。由于其高稳定性和催化效率,特别是作为一种多相催化剂将对硝基苯酚(p-NP)还原为对氨基苯酚(p-AP), Au-CNT的合成受到了广泛的关注。然而,文献中报道的大多数Au-CNT制备工艺都很耗时或需要昂贵的仪器。在本工作中,Au-CNT催化剂是通过一种简单、低成本的沉积-沉淀(DP)方法合成的。本研究的目的是评价pH和老化时间对Au-CNTs催化剂催化活性的影响。采用简单的沉积-沉淀法合成了Au-CNT纳米复合催化剂,并通过布鲁诺尔-埃米特-泰勒分析、傅里叶变换红外光谱、原子吸收光谱、热重分析、场发射扫描电镜和透射电镜对其进行了表征。在合成过程中,通过改变pH和老化时间,可以很容易地控制Au纳米颗粒的粒径和在CNTs上的负载。在过量硼氢化钠(NaBH4)存在下,纳米复合催化剂对硝基苯酚还原为对氨基苯酚表现出优异的催化活性。拟一级动力学模型得到的最高速率常数(k)为1.2 × 10-3 s-1。本研究为大规模应用提供了一种简单、经济的方法来合成稳定性高、催化效率高的Au-CNT催化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimized Preparation of Gold Nanoparticles-loaded Carbon Nanotubes (Au-CNTs) as an Efficient Catalyst for p-Nitrophenol Reduction
The current work aims to enhance the catalytic performance of gold nanopar-ticle–carbon nanotube (Au-CNT) composites towards the reduction of p-nitrophenol. The synthesis of Au-CNT has received extensive attention because of their high stability and catalytic efficiency, particularly as a heterogeneous catalyst in the reduction of p-nitrophenol (p-NP) to p-aminophenol (p-AP) However, most of the Au-CNT preparation processes reported in the literature are time-consuming or require expensive instrumentation. In the present work, Au-CNT catalysts were synthesized via a straightforward, low-cost deposition–precipitation (DP) method. The aim of the study was to evaluate the effect of pH and aging time on catalytic activity of Au-CNTs catalyst. The Au-CNT nanocomposite catalysts were synthesized using a simple deposition–precipitation method and characterized by Brunauer–Emmett–Teller analysis, fourier transform infrared spectroscopy, atomic absorption spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy, and trans-mission electron microscopy. The particle size and the loading of Au nanoparticles on the CNTs can be easily controlled by varying the pH and aging time during the synthesis process. The nanocomposite catalysts exhibited excellent catalytic activity for the reduction of p-nitrophenol to p-aminophenol in the presence of excess sodium borohydride (NaBH4). The highest rate constant (k) achieved based on the pseudo-first-order kinetic model was 1.2 × 10-3 s-1. This study offers a simple and cost-effective route to synthesize Au-CNT catalysts with high stability and catalytic efficiency for large-scale applica-tions.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信