scholarly journals Enhanced Degradation of Rhodamine B by Metallic Organic Frameworks Based on NH2-MIL-125(Ti) under Visible Light

Materials ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 7741
Author(s):  
Hong-Tham Nguyen Thi ◽  
Kim-Ngan Tran Thi ◽  
Ngoc Bich Hoang ◽  
Bich Thuy Tran ◽  
Trung Sy Do ◽  
...  

Samples of the bimetallic-based NH2-MIL-125(Ti) at a ratio of Mn+/Ti4+ is 0.15 (Mn+: Ni2+, Co2+ and Fe3+) were first synthesized using the solvothermal method. Their fundamental properties were analyzed by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectra, scanning electron microscopy (SEM), N2 adsorption–desorption measurements, and UV–Vis diffuse reflectance spectroscopy (UV-Vis DRS). The as-acquired materials were used as high-efficiency heterogeneous photocatalysts to remove Rhodamine B (RhB) dye under visible light. The results verified that 82.4% of the RhB (3 × 10−5 M) was degraded within 120 min by 15% Fe/Ti−MOFs. Furthermore, in the purpose of degrading Rhodamine B (RhB), the rate constant for the 15% Fe/Ti-MOFs was found to be 2.6 times as fast as that of NH2-MIL-125(Ti). Moreover, the 15% Fe/Ti-MOFs photocatalysts remained stable after three consecutive cycles. The trapping test demonstrated that the major active species in the degradation of the RhB process were hydroxyl radicals (HO∙) and holes (h+).

2014 ◽  
Vol 809-810 ◽  
pp. 890-894
Author(s):  
Dan Li ◽  
Lian Wei Shan ◽  
Gui Lin Wang ◽  
Li Min Dong ◽  
Wei Li ◽  
...  

Boron-BiVO4 samples were synthesized by sol-gel method. They were characterized by UV-vis diffuse reflectance spectroscopy, X-ray diffraction. Photocatalytic activity of the obtained BiVO4 samples was investigated through degrading methylene blue (MB). The results reveal that boron-BiVO4 catalysts have monoclinic scheelite structure. The BiVO4 and Co-BiVO4 photocatalysts were responsive to visible light. Co-BiVO4 photocatalyst showed higher photocatalytic activity than pure BiVO4, resulting in the significantly improved efficiency of degradation of MB.


2019 ◽  
Vol 12 (06) ◽  
pp. 1950085 ◽  
Author(s):  
Di Zhao ◽  
Xuezheng An ◽  
Yaxian Sun ◽  
Guihua Li ◽  
Hongyan Liu ◽  
...  

p-n heterojunction Ag2CO3/Ag3PO4/Ni thin films were prepared by electrochemical co-deposition. The surface morphology and structural properties of the thin films were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS). The photocatalytic (PC) properties of the Ag2CO3/Ag3PO4/Ni composite thin films were investigated by their ability to degrade rhodamine B (RhB) and Congo red (CR) under visible light irradiation. The results showed that the photodegradation efficiency of RhB by an Ag2CO3/Ag3PO4/Ni thin film under visible-light irradiation for 30[Formula: see text]min (98.84%) was 2.64 times higher than that of an Ag3PO4/Ni thin film and 3.44 times higher than of an Ag2CO3/Ni thin film. The presence of a [Formula: see text]-[Formula: see text] heterojunction greatly increased the charge conductivity of the film and its ability to photocatalytically reduce dissolved oxygen, which are the main reasons for the improved PC performance of the Ag2CO3/Ag3PO4/Ni films.


2014 ◽  
Vol 636 ◽  
pp. 7-10 ◽  
Author(s):  
Pei Song Tang ◽  
Chao Wan Tang ◽  
Jia Ni Ying ◽  
Dong Jing Ni ◽  
Qian Yang ◽  
...  

Using Fe (NO3)3⋅9H2O, Y(NO3)3⋅6H2O and citric acid as the main raw material, the YFeO3 nanoparticles were synthesized by ultrasonic assisted process and calcination. The YFeO3 nanoparticles were characterized by thermogravimetry and differential thermal analysis (TG-DTA), powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-visible diffuse reflectance spectroscopy (DRS). The results show that the perovskite structureYFeO3 (YFeO3-800) can be obtained through the calcination of ultrasonic processed YFeO3 precursors at 800 °C, and the resulting product has a particle size of 70 nm and an optical band gap of 2.0 eV. Consequently, the YFeO3-800 nanoparticles show high photocatalytic activity for decomposition of methyl orange under visible-light irradiation.


2021 ◽  
Vol 11 (1) ◽  
pp. xx-xx
Author(s):  
Nga Phan To ◽  
Lien Nguyen Hong ◽  
Tuyen Le Van ◽  
Nhan Phan Chi ◽  
Huyen Phan Thanh

Porous LaFeO3 were synthesised by nanocasting method using mesoporous silica (SBA-15) as a hard template and used as a visible-light-driven photocatalyst. The as-synthesised LaFeO3 photocatalyst were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray Diffraction (XRD), N2 adsorption-desorption, and Ultraviolet–Visible Diffuse Reflectance Spectroscopy (UV-vis DRS). The photo-Fenton catalytic activities of porous LaFeO3 were investigated for the degradation of oily-containing wastewater. The results showed that porous LaFeO3 had better photo-Fenton catalytic activity under visilbe light irradiation than pure LaFeO3. The remarkable improvement photo-Fenton catalytic activity of porous LaFeO3 material could be attributed to the synergistic effect of adsorption and visible light photo-Fenton processes thanks to its porous structure.


2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
P. Nyamukamba ◽  
L. Tichagwa ◽  
S. Mamphweli ◽  
L. Petrik

Herein, we report the synthesis of quartz supported TiO2 photocatalysts codoped with carbon and silver through the hydrolysis of titanium tetrachloride followed by calcination at 500°C. The prepared samples were characterized by UV-Vis diffuse reflectance spectroscopy, high resolution scanning electron microscopy (HRSEM), Raman spectroscopy, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD). Codoping of TiO2 with Ag and carbon resulted in an increase in the surface area of the photocatalyst and altered the ratio of the anatase to rutile phase. The absorption edge of all the doped TiO2 photocatalysts redshifted and the band gap was reduced. The lowest band gap of 1.95 eV was achieved by doping with 0.5% Ag. Doping TiO2 using carbon as the only dopant resulted in a quartz supported photocatalyst that showed greater photocatalytic activity towards methyl orange than undoped TiO2 and also all codoped TiO2 photocatalysts under visible light irradiation.


2015 ◽  
Vol 2015 ◽  
pp. 1-6
Author(s):  
Liqin Qin ◽  
Pingfang Tao ◽  
Xiaosong Zhou ◽  
Qi Pang ◽  
Chunjie Liang ◽  
...  

A facile method for the synthesis of Ag3PO4visible light photocatalyst has been developed to improve the photocatalytic activity and stability. The as-prepared samples are investigated by X-ray powder diffraction, scanning electron microscopy, infrared spectroscopy, photoluminescence (PL) spectroscopy, and UV-Vis diffuse reflectance spectroscopy techniques. The results reveal that the prepared Ag3PO4has cube structure with a band gap of 2.26 eV. The as-prepared samples show higher photocatalytic activity for methylene blue (MB) degradation than that of N-TiO2under visible light irradiation.


2017 ◽  
Vol 75 (7) ◽  
pp. 1523-1528 ◽  
Author(s):  
Hongfeng Zhang ◽  
Xiu He ◽  
Weiwei Zhao ◽  
Yu Peng ◽  
Donglan Sun ◽  
...  

Fe3O4/TiO2 magnetic mesoporous composites were synthesized through a sol-gel method with tetra-n-butyl titanate as precursor and surfactant P123 as template. The as-prepared Fe3O4/TiO2 composites were characterized by X-ray diffraction, diffuse reflectance spectroscopy, nitrogen adsorption-desorption isotherm and pore size distribution. The as-synthesized products were applied as photocatalysis for the degradation of Acid Black ATT and tannery wastewater under UV lamp irradiation. Fe3O4/TiO2-8 composites containing Fe3O4 of 8 wt% were selected as model catalysts. The optimal catalyst dosage was 3 g/L in this photocalytic system. The magnetic Fe3O4/TiO2 composites possessed good photocatalytic stability and durability. This approach may provide a platform to prepare a magnetic composite to optimize the catalytic ability.


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Wang Ling-Li ◽  
Ma Wan-Hong ◽  
Wang Shu-Lian ◽  
Zhang Yu ◽  
Jia Man-Ke ◽  
...  

BiOBr nanoplates, marked asα-BiOBr andβ-BiOBr, were synthesized via hydrothermal method using cetylpyridinium bromide (CPB) and NaBr as reactants, respectively. X-Ray Diffraction (XRD), transmission electron microscope (TEM), N2adsorption/desorption, UV-visible diffuse reflectance spectroscopy (UV-Vis DRS), and cyclic voltammetry (CV) were employed to characterize the obtained BiOBr. The results showed thatα-BiOBr andβ-BiOBr can absorb visible light and both the band gaps of them were about 2.76 eV. Under visible light irradiation, the photodegradation of organic dye sulforhodamine (SRB) and salicylic acid (SA) usingα-BiOBr andβ-BiOBr as the catalysts was carried out. The reaction kinetic constants of the degradation of SRB byα-BiOBr andβ-BiOBr were 0.00602 min−1and 0.0047 min−1, respectively, which indicated that the photocatalytic activity ofα-BiOBr was higher than that ofβ-BiOBr. The UV-Vis DRS and total organic carbon (TOC) were also monitored, and the TOC removal rate ofα-BiOBr andβ-BiOBr was 86% and 48%, respectively. At the same time, hydrogen peroxide (H2O2) and active radicals were measured and analyzed, which showed that the main active species wasOH∙during the photocatalytic reaction.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Yunling Zou ◽  
Xianshou Huang ◽  
Tao Yu ◽  
Xiaoqiang Tong ◽  
Yan Li ◽  
...  

Abstract Cu-doped TiO2 having a brookite phase and showing enhanced visible light photocatalytic activity was synthesized using a mild solvothermal method. The as-prepared samples were characterized by various techniques, such as X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy. Photocatalytic activity of Cu-doped brookite TiO2 nanoparticles was evaluated by photodegradation of methylene blue under visible light irradiation. The X-ray diffraction analysis showed that the crystallite size of Cu-doped brookite TiO2 samples decreased with the increase of Cu concentration in the samples. The UV-Vis diffuse reflectance spectroscopy analysis of the Cu-doped TiO2 samples showed a shift to lower energy levels in the band gap compared with that of bare phase brookite TiO2. Cu doped brookite TiO2 can obviously improve its visible light photocatalytic activity because of Cu ions acting as electron acceptors and inhibiting electron-hole recombination. The brookite TiO2 sample with 7.0 wt.% Cu showed the highest photocatalytic activity and the corresponding degradation rate of MB (10 mg/L) reached to 87 % after visible light illumination for 120 min, much higher than that of bare brookite TiO2 prepared under the same conditions (78 %).


2015 ◽  
Vol 1118 ◽  
pp. 242-250 ◽  
Author(s):  
Zhen Wu Ding ◽  
Si Chen ◽  
Zhong Qing Liu ◽  
Cheng Fa Jiang ◽  
Wei Chu

Mesoporous S-doped TiO2 microspheres were synthesized via hydrothermal method using Ti (SO4)2 precursor and urea as homogeneous precipitate agent. The TiO2-based catalyst samples were characterized by means of Field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), N2 adsorption/desorption and UV-vis diffuse reflectance spectra (UV-vis DRS). Photo-catalytic experiments were carried out by catalytic degradation of methylene blue aqueous solution under visible light. It was found that the S-doped TiO2 microspheres gave better photo-catalytic performances. The higher absorbance in the visible region explained this phenomenon. There was an appropriate Ti (SO4)2 amount for the catalyst with better photo-catalytic degradation.


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