Biosynthesis of TiO2 nanoparticles by Acalypha indica; photocatalytic degradation of methylene blue

被引:23
作者
Chinnathambi, Arunachalam [1 ]
Vasantharaj, Seerangaraj [2 ]
Saravanan, Mythili [2 ]
Sathiyavimal, Selvam [3 ]
Pham Anh Duc [4 ]
Nasif, Omaima [5 ]
Alharbi, Sulaiman Ali [1 ]
Nguyen Thuy Lan Chi [6 ]
Brindhadevi, Kathirvel [6 ]
机构
[1] King Saud Univ, Coll Sci, Dept Bot & Microbiol, POB 2455, Riyadh 11451, Saudi Arabia
[2] Hindusthan Coll Arts & Sci, Dept Biotechnol, Coimbatore 641028, Tamil Nadu, India
[3] CORX Lifesci & Pharmaceut Private Ltd, Tiruchirappalli, Tamil Nadu, India
[4] Ton Duc Thang Univ, Fac Environm & Labour Safety, Ho Chi Minh City, Vietnam
[5] King Saud Univ, King Khalid Univ Hosp, Coll Med, Dept Physiol,Med City, POB 2925, Riyadh 11461, Saudi Arabia
[6] Ton Duc Thang Univ, Fac Environm & Labour Safety, Innovat Green Prod Synth & Renewable Environm Dev, Ho Chi Minh City, Vietnam
关键词
Acalypha indica; TiO2; FESEM; Photocatalyst; Nanoparticles;
D O I
10.1007/s13204-021-01761-3
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Now a day the green synthesis of TiO2 nanoparticles has several advantages over synthetic methods such as ecofriendly, cost-effective and nonhazardous. In this study, Acalypha indica has been used for the synthesis of TiO2. TiO2 nanoparticles were characterized using ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), and field emission scanning electron microscopy (FESEM). In UV spectra, wide band appeared at 333 nm. FTIR spectra confirmed the presence of alcohol group (3364.53 & 3448.83 cm(-1)), alkane group (2872.73 & 2970.83 cm(-1)) and strong C-O stretch (1092.93 & 1113.28 cm(-1)). XRD peaks showed that synthesized TiO2 nanoparticles have both anatase and rutile phase. The surface morphology of the TiO2 was studied using FESEM which showed a porous surface on the nanoparticles. Since TiO2 is a well-known photocatalyst, methylene blue dye has been used for the investigation of photocatalytic activity.
引用
收藏
页码:383 / 390
页数:8
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