scholarly journals Porous Polymer-Titanium Dioxide/Copper Composite with Improved Photocatalytic Activity toward Degradation of Organic Pollutants in Wastewater: Fabrication and Characterization as Well as Photocatalytic Activity Evaluation

Catalysts ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 310 ◽  
Author(s):  
Qijie Xu ◽  
Yan Wang ◽  
Mei Chi ◽  
Wenbin Hu ◽  
Ning Zhang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Titanium Dioxide ◽  
Photocatalytic Activity ◽  
Organic Pollutants ◽  
Photocatalytic Performance ◽  
Hydrothermal Process ◽  
Porous Polymer ◽  
Tetrabutyl Titanate ◽  
Simulated Sunlight ◽  
Sunlight Irradiation

Titanium dioxide (TiO2) and TiO2/copper (denoted as TC) composite were prepared via hydrothermal process. In the meantime, divinylbenzene (DVB) and bismaleimide (BMI) monomers were allowed to participate in in-situ radical polymerization in the presence of azobisisobutyronitrile (AIBN) initiator to afford porous polymers (abridged as PP). The as-obtained PP were mixed together with tetrabutyl titanate (TBT) and CuSO4·5H2O in vacuum to obtain PP/TC composite (denoted as PPTC) containing incorporated TC composite in the pores of PP. The as-prepared TiO2, TC, and PPTC were characterized by transmission electron microscopy, scanning electron microscopy, X-ray diffraction, fluorescence spectrometry, and electron spin resonance spectrometry, and so on. Furthermore, their photocatalytic activity for the degradation of N,N-dimethylformamide, methyl orange, phenol, and methylene blue under the irradiation of simulated sunlight (Xe lamp light) and natural sunlight were investigated. Findings indicated that, whether under simulated sunlight or nature sunlight irradiation, PPTC exhibited much better photocatalytic performance than TiO2 and TC for the degradation of the tested organic pollutants. Particularly, it allowed N,N-dimethylformamide (DMF) to be degraded by a rate of 73.7% under simulated sunlight irradiation and it retained photocatalytic activity even after six cycles of reuse, exhibiting promising potential for the removal of organic pollutants in wastewater (including industrial water, aquaculture wastewater, and domestic sewage). The desired photocatalytic performance of the as-prepared PPTC is attributed to two aspects. Namely, the incorporation of Cu2+ into the fine structure of TiO2 contributes to increasing photocatalyst activity and producing more free radical while the embedding of TC composite into the PP pores improves to the contact area between the photocatalyst and organic pollutants, and both are beneficial for improving the adsorption capacity and activity of the photocatalyst, thereby enhancing the degradation of the organic pollutants.

scholarly journals Combination of mesoporous titanium dioxide with MoS2 nanosheets for high photocatalytic activity

2017 ◽  
Vol 19 (2) ◽  
pp. 56-60 ◽  
Author(s):  
Loghman Karimi
Keyword(s):  
Electron Microscopy ◽  
Titanium Dioxide ◽  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Dye Degradation ◽  
Hydrothermal Process ◽  
Bet Analysis ◽  
Mesoporous Titanium Dioxide

Abstract This study presents a facile approach for the preparation of MoS2 nanosheet decorated by porous titanium dioxide with effective photocatalytic activity. Mesoporous titanium dioxide nanostructures first synthesized by a hydrothermal process using titanium (III) chloride and then the MoS2/TiO2 were prepared through mixing of MoS2 nanosheet with mesoporous titanium dioxide under ultrasonic irradiation. The synthesized nanocomposite was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), and Brunauer-Emmett-Teller (BET) analysis. The results showed that the nanocomposite has mesoporous structure with specific surface area of 176.4 m2/g and pore diameter of 20 nm. The as-prepared MoS2/TiO2 nanocomposites exhibited outstanding photocatalytic activity for dye degradation under sunlight irradiation, which could be attributed to synergistic effect between the molybdenum disulfide nanosheet and mesoporous titanium dioxide. The photocatalytic performance achieved is about 2.2 times higher than that of mesoporous TiO2 alone. It is believed that the extended light absorption ability and the large specific surface area of the 2D MoS2 nanosheets in the nanocomposite, leading to the enhanced photocatalytic degradation activity.

scholarly journals Growth Process and CQDs-modified Bi4Ti3O12 Square Plates with Enhanced Photocatalytic Performance

Micromachines ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 66 ◽  
Author(s):  
Xinxin Zhao ◽  
Hua Yang ◽  
Ziming Cui ◽  
Xiangxian Wang ◽  
Zao Yi
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Growth Process ◽  
Photocatalytic Performance ◽  
Simulated Sunlight ◽  
Hydrothermal Route ◽  
Electron Hole ◽  
X Ray ◽  
Photocurrent Spectroscopy

Bi4Ti3O12 square plates were synthesized via a hydrothermal route, and their growth process was systematically investigated. Carbon quantum dots (CQDs) were prepared using glucose as the carbon source, which were then assembled on the surface of Bi4Ti3O12 square plates via a hydrothermal route with the aim of enhancing the photocatalytic performance. XRD (X-ray powder diffraction), SEM (scanning electron microscopy), TEM (transmission electron microscopy), UV-vis DRS (diffuse reflectance spectroscopy), XPS (X-ray photoelectron spectroscopy), FTIR (Fourier transform infrared spectroscopy), PL (photoluminescence) spectroscopy, EIS (electrochemical impedance spectroscopy) and photocurrent spectroscopy were used to systematically characterize the as-prepared samples. It is demonstrated that the decoration of CQDs on Bi4Ti3O12 plates leads to an increased visible light absorption, slightly increased bandgap, increased photocurrent density, decreased charge-transfer resistance, and decreased PL intensity. Simulated sunlight and visible light were separately used as a light source to evaluate the photocatalytic activity of the samples toward the degradation of RhB in aqueous solution. Under both simulated sunlight and visible light irradiation, CQDs@Bi4Ti3O12 composites with an appropriate amount of CQDs exhibit obviously enhanced photocatalytic performance. However, the decoration of excessive CQDs gives rise to a decrease in the photocatalytic activity. The enhanced photocatalytic activity of CQDs-modified Bi4Ti3O12 can be attributed to the following reasons: (1) The electron transfer between Bi4Ti3O12 and CQDs promotes an efficient separation of photogenerated electron/hole pairs in Bi4Ti3O12; (2) the up-conversion photoluminescence emitted from CQDs could induce the generation of additional electron/hole pairs in Bi4Ti3O12; and (3) the photoexcited electrons in CQDs could participate in the photocatalytic reactions.

Study on the effect of water contents on the formation of nanostructured porphyrins via self-assembly and their application for the degradation of organic dyes

2021 ◽  
Vol 10 (3) ◽  
pp. xx-xx
Author(s):  
Anh Nguyen Tuan ◽  
Khiem Le Dinh ◽  
Quynh Tran Nhu ◽  
Tuan Truong Ngoc ◽  
Ha Ninh Duc ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Self Assembly ◽  
Photocatalytic Performance ◽  
Organic Dyes ◽  
Simulated Sunlight ◽  
Sunlight Irradiation ◽  
Water Fraction ◽  
Vis Spectroscopy ◽  
Water Contents ◽  
Scanning Electron

In this work, the THF/H2O mixture was employed to synthesize the nanostrucuted 5,10,15,20-tetra(3,4,5-trimethoxyphenyl) porphyrin (TTOP) via solvophobic self-assembly. The resultant porphyrin nanomaterial was characterized using photoluminescence (PL), UV-vis spectroscopy, and scanning electron microscopy (SEM). The prepared self-assembled porphyrin was in structures of rod-like, cubic-lik, and particles forms. These porphyrin crystals showed high photocatalytic performance for the degradation of RhB under simulated sunlight irradiation, especially with the porphyrin crystal formed with the water fraction of 80 and 90%.

One-Pot Hydrothermal Synthesis of g-C3N4/BiPO4 Nanocomposites with Significant Photocatalytic Activity

2020 ◽  
Vol 20 (5) ◽  
pp. 3047-3052 ◽  
Author(s):  
Zhen-Zhao Pei ◽  
Pei Wang ◽  
Chao-Yang Li ◽  
Xiao-Liang Li ◽  
Yong-Wu He ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Diffuse Reflectance ◽  
Organic Dyes ◽  
Hydrothermal Process ◽  
Simulated Sunlight ◽  
X Ray Diffraction ◽  
One Pot ◽  
Sunlight Irradiation ◽  
X Ray ◽  
Scanning Electron

The g-C3N4/BiPO4 composites have been successfully synthesized via a one-pot hydrothermal process, which can be used to degrade the organic dyes (rhodamine B and methylene blue) under simulated sunlight irradiation. X-ray diffraction (XRD), scanning electron microscope (SEM), UV-Vis diffuse reflectance spectra and Fourier transform infrared (FTIR) spectroscopy have been employed to characterize the samples. The g-C3N4/BiPO4 composites exhibited higher photocatalytic activity than pure BiPO4. And the optimum photocatalyst shows the outstanding photocatalytic activity, which exhibited 99.0% and 86.6% decolorization rate of RhB and MB, respectively.

scholarly journals Ag2CO3 Decorating BiOCOOH Microspheres with Enhanced Full-Spectrum Photocatalytic Activity for the Degradation of Toxic Pollutants

Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 914 ◽  
Author(s):  
Shijie Li ◽  
Liuye Mo ◽  
Yanping Liu ◽  
Huiqiu Zhang ◽  
Yaming Ge ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Environmental Remediation ◽  
Photocatalytic Performance ◽  
Type I ◽  
Simulated Sunlight ◽  
Practical Application ◽  
Pollutant Degradation ◽  
Full Spectrum ◽  
Sunlight Irradiation ◽  
Toxic Pollutants

The development of excellent full-spectrum photocatalysts is of vital significance to its practical application in environmental remediation. Herein, flower-like Ag2CO3/BiOCOOH type I heterostructures were prepared via a facile method and exhibited powerful photocatalytic activity by removing various toxic pollutants (rhodamine B, methyl blue, and tetracycline hydrochloride) under simulated sunlight irradiation. The boosted photocatalytic performance is attributed to the expanded range of the absorption spectrum and alleviated separation rate of the photo-induced electrons and holes. The photoluminescence spectra and trapping experiment were applied to clarify the photocatalytic reaction mechanism of Ag2CO3/BiOCOOH. The holes and •O2− were detected as the dominant reactive species involved in pollutant degradation. This work provides a novel full-spectrum-driven photocatalyst of Ag2CO3/BiOCOOH, which could effectively degrade toxic pollutants under simulated sunlight.

Sodium Dodecyl Benzene Sulfonate-assisted Synthesis and Natural Sunlight Photocatalytic Activity of La Bismuthate Nanorods

2020 ◽  
Vol 16 (5) ◽  
pp. 805-815
Author(s):  
Fanglv Qiu ◽  
Zi Wang ◽  
Hongjun Chen ◽  
Yue Ma ◽  
Hang Wu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Organic Pollutants ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectrum ◽  
Sodium Dodecyl ◽  
Sodium Dodecyl Benzene Sulfonate ◽  
Hydrothermal Temperature ◽  
Sunlight Irradiation ◽  
Dodecyl Benzene Sulfonate ◽  
Good Photocatalytic Performance

Background: Removal of the organic pollutants using the photo-catalysts by the photocatalytic treatment process under natural sunlight irradiation has attracted great attention owing to the complete destruction of the organic pollutants. The La bismuthate nanorods possess good photocatalytic performance for the removal of the methylene orange (MO) under the sunlight irradiation. Objective: The aim is to synthesize La bismuthate nanorods by hydrothermal method and research the photocatalytic performance of the La bismuthate nanorods for MO degradation under sunlight irradiation. Methods: La bismuthate nanorods have been synthesized by a simple sodium dodecyl benzene sulfonate (SDBS)-assisted hydrothermal method using sodium bismuthate and La acetate as the starting materials. The obtained La bismuthate products were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy and solid UV-vis diffuse reflectance spectrum. Results: With different SDBS concentration, hydrothermal temperature and reaction time, different morphologies of the La bismuthate products were obtained. XRD analysis shows that the La bismuthate nanorods obtained from 180°C for 24 h with 5wt.% SDBS are composed of orthorhombic La1.08Bi0.92O3.03 phase. Electron microscopy observations show that the La bismuthate nanorods with flat tips have the length of longer than 10 μm and diameter of about 20-100 nm, respectively. The morphology and structure of the products are closely related to the SDBS concentration, hydrothermal temperature and reaction time. Solid UV-vis diffuse reflectance spectrum shows that the band gap of the La bismuthate nanorods is 2.37 eV. The La bismuthate nanorods show good photocatalytic performance for the degradation of MO under the sunlight irradiation. MO solution with the concentration of 10 mg.L-1 can be totally removed by 10 mg La bismuthate nanorods in 10 mL MO aqueous solution under sunlight irradiation for 6 h. Conclusion: The photocatalytic performance for the removal of MO is dependent on the sunlight irradiation time and dosage of the La bismuthate nanorods. The La bismuthate nanorods exhibit great potential for the removal of organic pollutants.

Electrospun TiO2 embedded nanofibers for photocatalytic applications

2019 ◽  
Vol 34 (01n03) ◽  
pp. 2040015
Author(s):  
Junyao Wu ◽  
Alexandre Pernin ◽  
Yixuan Wang ◽  
Han Wang ◽  
Jun Yao ◽  
...  
Keyword(s):  
Titanium Dioxide ◽  
Photocatalytic Activity ◽  
Environmental Remediation ◽  
Low Cost ◽  
High Reactivity ◽  
Simulated Sunlight ◽  
Electrospinning Technique ◽  
Sunlight Irradiation ◽  
Text Content ◽  
Photocatalytic Applications

The development of photocatalysts with low cost, high reactivity and easy recovery provides great potentials for environmental remediation. In this study, polyacrylonitrile (PAN) nanofibers containing titanium dioxide ([Formula: see text]) nanoparticles were successfully fabricated using a facile electrospinning technique. The effects of [Formula: see text] content, PAN concentration and thermal treatment on the adsorption and photocatalysis properties of [Formula: see text] nanofibers have been investigated. The results indicate that the embedded [Formula: see text] nanofibers possess the property to effectively decompose rhodamine B (RhB) under simulated sunlight irradiation. The enhanced photocatalytic activity can be attributed to the loading of [Formula: see text] nanoparticles and the property of polymer matrix.

scholarly journals Study on Synthesis and Photocatalytic Activity of Porous Titania Nanotubes

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Huang Liu ◽  
Yanhua Zhang ◽  
Hongtao Yang ◽  
Wei Xiao ◽  
Lanlan Sun
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Filter Paper ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Cellulose Nanofibers ◽  
Titania Nanotubes ◽  
Tetrabutyl Titanate ◽  
X Ray ◽  
Porous Titania

Using the common natural cellulose substance (filter paper) and triblock copolymer (Pluronic P123) micelles as dual templates, porous titania nanotubes with enhanced photocatalytic activity have been successfully synthesized through sol-gel methods. Firstly, P123 micelles were adsorbed onto the surfaces of cellulose nanofibers of filter paper, followed by hydrolysis and condensation of tetrabutyl titanate around these micelles to form titania layer. After calcination to remove the organic templates, hierarchical titania nanotubes with pores in the walls were obtained. The sample was characterized by X-ray diffraction pattern (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption/desorption, Fourier Transform Infrared Spectroscopy (FT-IR), Ultraviolet-Visible Diffuse Reflectance Spectroscopy (UV-Vis DRS), and X-ray photoelectron spectroscopy (XPS). As compared with commercial P25 catalyst, the porous titania nanotubes prepared by this method displayed significantly enhanced photocatalytic activity for degrading methyl orange under UV irradiation. Within 10 minutes, the porous titania nanotubes are able to degrade over 70% of the original MO, while the value for the commercial Degussa P25 is only about 33%.

The Study on the Influential Factors of Photocatalytic Performance of Eosin-Sensitized TiO2 Nanoparticles

2013 ◽  
Vol 827 ◽  
pp. 3-7
Author(s):  
Shun Jiang He ◽  
Xue Yan Du ◽  
Qiao Wang ◽  
Jing Xu
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Photocatalytic Degradation ◽  
Degradation Rate ◽  
Photocatalytic Performance ◽  
Influential Factors ◽  
Sunlight Irradiation ◽  
Sensitization Time

The photocatalytic activity of eosin-sensitized TiO2 nanoparticles on photocatalytic degradation rate (PDR) of methyl orange under sunlight irradiation was studied. The influential factors on the degradation, such as eosin concentration, TiO2 dosage, sensitization time and sensitization temperature were also investigated. The results show that: The performance of TiO2 nanoparticles for PDR of methyl orange has been improved obviously for eosin sensitizing. The PDR of methyl orange reached 45.28% under the conditions of eosin concentration of 20mg/L, TiO2 dosage of 0.5000g/L, sensitization time of 24h and sensitization temperature of 20°C.

scholarly journals One-step synthesis of OH-TiO 2 /TiOF 2 nanohybrids and their enhanced solar light photocatalytic performance

2018 ◽  
Vol 5 (6) ◽  
pp. 172005 ◽  
Author(s):  
Chentao Hou ◽  
Wenli Liu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Performance ◽  
Performance Enhancement ◽  
Hydrothermal Process ◽  
Emission Spectra ◽  
Solar Light ◽  
Dominant Factor ◽  
Simulated Solar Light ◽  
Transmission Electron ◽  
Naoh Treatment

TiO 2 /TiOF 2 nanohybrids were quickly synthesized through a hydrothermal process using titanium n-butoxide (TBOT), ethanol (C 2 H 5 OH) and hydrofluoric acid as precursors. The prepared nanohybrids underwent additional NaOH treatment (OH-TiO 2 /TiOF 2 ) to enhance their photocatalytic performance. In this paper, the mechanism of NaOH affecting the pathway of transformation from TBOT (Ti precursor) to TiO 2 nanosheets was discussed. The synthesized TiO 2 /TiOF 2 and OH-TiO 2 /TiOF 2 were characterized by field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction pattern (XRD), Fourier infrared spectroscopic analysis (FT-IR), Photoluminescence (PL) emission spectra and UV–visible diffuse reflection spectra (UV–vis DRS). The photocatalytic activity and stability of synthesized samples were evaluated by degradation of methylene blue (MB) under the simulated solar light. The results showed that a larger ratio of TiO 2 to TiOF 2 in TiO 2 /TiOF 2 and OH-TiO 2 /TiOF 2 nanohybrids could allow for even higher MB conversion compared with only TiO 2 nanosheets. NaOH treatment can wash off the F ions from TiOF 2 and induce this larger ratio. The highest efficiency of MB removal was just above 90% in 1 h. Lower electron–hole pairs recombination rate is the dominant factor that induces the photocatalytic performance enhancement of TiO 2 /TiOF 2 nanohybrids. The synthesized OH-TiO 2 /TiOF 2 nanohybrids exhibit great potential in the abatement of organic pollutants.

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