One-pot synthesis of highly stable and concentrated silver nanoparticles with enhanced catalytic activity

被引:28
|
作者
Hussain, Fiaz [3 ]
Shaban, Samy M. [1 ,2 ]
Kim, Jinhwan [1 ]
Kim, Dong-Hwan [1 ,2 ]
机构
[1] Sungkyunkwan Univ, Sch Chem Engn, Suwon 16419, South Korea
[2] Sungkyunkwan Univ, BICS, Suwon 16419, South Korea
[3] Sungkyunkwan Univ, Polymer Dept, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
One-pot Synthesis; Silver Nanoparticles; High Yield; Stability; Catalytic Activity; Methylene Blue; p-Nitrophenol; IN-SITU SYNTHESIS; GOLD NANOPARTICLES; AG NANOPARTICLES; POLYACRYLIC-ACID; FACILE SYNTHESIS; REDUCTION; 4-NITROPHENOL; WATER; OXIDE; MICROSPHERES;
D O I
10.1007/s11814-019-0270-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Well-dispersed silver nanoparticles (AgNPs) were synthesized using a benign, one-pot process based on a low-cost wet chemistry technique. Monoethanolamine was used as a strong reducing agent and poly(acrylic acid) (PAA) was used as a stabilizing agent. After the addition of these reagents to a reaction system, one-pot synthesis of AgNPs was completed in approximate to 45 min at 75 degrees C with a reaction efficiency of 92.4%. The average particle size of the aqueous dispersion of AgNPs was 14.83 +/- 5.96 nm, and the dispersion remained stable even after 14 months in an ambient dark environment, which may be due to the electrostatic repulsion of the carboxylate anions of the stabilizing agent. The role of PAA in the stabilization of the AgNPs was analyzed via Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy. The highly stable AgNPs in the aqueous system showed high catalytic activity for the reduction of methylene blue and p-nitrophenol in the presence of sodium borohydride as the reducing agent based on pseudo-first-order kinetics.
引用
收藏
页码:988 / 995
页数:8
相关论文
共 50 条
  • [41] One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles
    Liu, Qiong-Jie
    Yan, Wen-Guang
    Wang, Lijia
    Zhang, X. Peter
    Tang, Yong
    ORGANIC LETTERS, 2015, 17 (16) : 4014 - 4017
  • [42] One-Pot Synthesis and Antiproliferative Activity of Highly Functionalized Pyrazole Derivatives
    Lusardi, Matteo
    Rotolo, Chiara
    Ponassi, Marco
    Iervasi, Erika
    Rosano, Camillo
    Spallarossa, Andrea
    CHEMMEDCHEM, 2022, 17 (05)
  • [43] One-Pot Catalytic Asymmetric Synthesis of Pyranones
    Cheng, Kevin
    Kelly, Ann Rowley
    Kohn, Rachel A.
    Dweck, Jessica F.
    Walsh, Patrick J.
    ORGANIC LETTERS, 2009, 11 (12) : 2703 - 2706
  • [44] A facile, one-pot synthesis of highly branched Au nanocorals and their enhanced electrocatalytic activity for ethanol oxidation
    Liu, Zhenyuan
    Fu, Gengtao
    Tang, Yawen
    Sun, Dongmei
    Chen, Yu
    Lu, Tianhong
    CRYSTENGCOMM, 2014, 16 (36): : 8576 - 8581
  • [45] A Catalytic One-Pot Synthesis of Indolyl Cyclobutanones
    Porcu, Stefania
    Rodriguez, Carla Aira
    Frongia, Angelo
    Secci, Francesco
    SYNTHESIS-STUTTGART, 2021, 53 (05): : 925 - 932
  • [46] One-pot, catalytic, asymmetric synthesis of polypropionates
    Calter, MA
    Guo, X
    Liao, WS
    ORGANIC LETTERS, 2001, 3 (10) : 1499 - 1501
  • [47] One-pot solvothermal synthesis of Ag nanoparticles decorated BiOCOOH microflowers with enhanced visible light activity
    Li, Shijie
    Hu, Shiwei
    Jiang, Wei
    Xu, Kaibing
    MATERIALS LETTERS, 2017, 196 : 343 - 346
  • [48] One-pot solvothermal synthesis of highly photoluminescent carbon nanoparticles and their photocatalytic application
    Li, Feng
    Wang, Guiyan
    Li, Hongren
    Li, Yongbo
    Zhou, Shiqi
    MATERIALS LETTERS, 2014, 122 : 352 - 354
  • [49] Facile one-pot green synthesis of Aloe vera mediated silver nanoparticles and their catalytic efficiency towards organic transformations
    Singh, Preeti
    Nisa, Kharu
    Nisha, Robin
    Choudhary, Robin
    Verma, Muskan
    ANALYTICAL CHEMISTRY LETTERS, 2024, 14 (03) : 319 - 331
  • [50] One-pot synthesis of ZnO/Ag nanospheres with enhanced photocatalytic activity
    Xie, Jinsong
    Wu, Qingsheng
    MATERIALS LETTERS, 2010, 64 (03) : 389 - 392