Green synthesis of copper nanoparticles using Cocoa pod extract and its catalytic activity in deep oxidation of aromatic hydrocarbons

被引:0
作者
Phung Anh Nguyen
Ai Vi Pham Nguyen
Trung Dang-Bao
Hong Phuong Phan
Thi Thuy Van Nguyen
Boi An Tran
Thanh Linh Duong Huynh
Tien Cuong Hoang
Van Tien Huynh
Tri Nguyen
机构
[1] Vietnam Academy of Science and Technology,Institute of Chemical Technology
[2] Vietnam National University Ho Chi Minh City,Graduate University of Science and Technology
[3] Ho Chi Minh City University of Technology (HCMUT),undefined
[4] Vietnam Academy of Science and Technology,undefined
[5] Ho Chi Minh City University of Food Industry,undefined
[6] Ho Chi Minh City Open University,undefined
来源
SN Applied Sciences | 2020年 / 2卷
关键词
Green synthesis; Copper nanoparticles; pod; Deep oxidation; Aromatic hydrocarbons;
D O I
暂无
中图分类号
学科分类号
摘要
An effective and green technique was performed for the synthesis of copper nanoparticles (CuNPs) from an organic resource using the Cocoa pod (CCP) extract as a reducing agent. The formation of CuNPs was confirmed by ultraviolet–visible absorption spectroscopy (UV–Vis) at the wavelength range of 500–600 nm. The optimized conditions for the synthesis of CuNPs using CCP extract as a reducing agent were determined by the volume ratio of Cu(NO3)2 solution/CCP extract of 3.5/1.5, stirring rate of 300 rpm, pH solution of 7.5, the temperature of 75 °C and the synthesis duration within 180 min. At these conditions, the X-ray diffraction result revealed a face-centered cubic structure of zero-valent copper with a highly crystalline and an average size of 34.4 nm. Fourier transform infrared spectroscopy result confirmed the presence of flavonoids, polyphenolic, and alkaloids components in CCP extract which can act as the reducing and stabilizing agents for CuNPs formation. At the optimized synthetic conditions, CuNPs loaded on various supports (Al2O3, CeO2, and TiO2) were prepared following the same protocol and then applied for catalytic deep oxidation of aromatic hydrocarbons (AHs). Among them, CeO2 was the best support in AHs deep oxidation, and the sample of 7.5Cu–Ce (7.5 wt% of CuNPs supported on CeO2) was the most efficient. Compared with 5Cu–Ce and 10Cu–Ce, the 7.5Cu–Ce sample exhibited a higher benzene conversion at a low temperature (275–325 °C) and reached the full conversions of benzene, toluene, ethylbenzene, and xylene (BTEX) to carbon dioxide and water vapor below 450 °C. Furthermore, the 7.5Cu–Ce sample showed great stability for such reactions at 300 °C as proven by the unchanged conversions of BTEX during 48 h.
引用
收藏
相关论文
共 172 条
[1]  
Adjin-Tetteh M(2018)Thermochemical conversion and characterization of cocoa pod husks a potential agricultural waste from Ghana Indl Crop Prod 119 304-312
[2]  
Asiedu N(2001)CuO–CeO Catal Letters 73 33-40
[3]  
Dodoo-Arhin D(2002) mixed oxide catalysts for the selective oxidation of carbon monoxide in excess hydrogen Catal Today 75 157-167
[4]  
Karam A(2016)A comparative study of Pt/γ-Al Bull Chem React Eng Catal 11 210-219
[5]  
Amaniampong PN(2005)O Taiwan J Air Waste Manage 55 1487-1497
[6]  
Avgouropoulos G(2011), Au/α-Fe Appl Surf Sci 257 4597-4602
[7]  
Ioannides T(1991)O Ani Feed Sci Tech 35 161-169
[8]  
Matralis HK(2017) and CuO–CeO Marmara Pharm J 21 866-871
[9]  
Batista J(2009) catalysts for the selective oxidation of carbon monoxide in excess hydrogen J Nat Gas Chem 18 179-182
[10]  
Hocevar S(2019)Production of CO-rich hydrogen gas from methane dry reforming over Co/CeO2 catalyst ACS Sensors 4 1358-1364