Photostability of TiO2-Coated Wool Fibers Exposed to Ultraviolet B, Ultraviolet A, and Visible Light Irradiation

Abstract This study is to investigate the role of the coating of TiO2 nanoparticles deposited on wool fibers against high-intensity ultraviolet B (UVB), ultraviolet A (UVA), and visible light irradiation. The properties of tensile and yellowness and whiteness indices of irradiated TiO2-coated wool fibers are measured. The changes of TiO2-coated wool fibers in optical property, thermal stability, surface morphology, composition, molecular structure, crystallinity, and orientation degree are characterized using diffuse reflectance spectroscopy, thermogravimetric analysis, scanning electronic microscopy, energy-dispersive X-ray spectroscopy, Fourier-transform infrared spectroscopy, and X-ray diffraction techniques. Experimental results show that the tensile properties of anatase TiO2-coated wool fibers can be degraded under the high-intensity UVB, UVA, and visible light irradiation for a certain time, resulting in the loss of the postyield region of stress–strain curve for wool fibers. The coating of TiO2 nanoparticles makes a certain contribution to the tensile property, yellowness and whiteness indices, thermal stability, and surface morphology of wool fibers against high-intensity UVB, UVA, and visible light irradiation. The high-intensity UVB, UVA, and visible light can result in the photo-oxidation deterioration of the secondary structure of TiO2-coated wool fibers to a more or less degree. Meanwhile, the crystallinity and orientation degree of TiO2 coated wool fibers decrease too.

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Cu Doped TiO2: Visible Light Assisted Photocatalytic Antimicrobial Activity and High Temperature Anatase Stability

10.26434/chemrxiv.7159733.v1 ◽

2018 ◽

Cited By ~ 2

Author(s):

Snehamol Mathew ◽

Priyanka Ganguly ◽

Stephen Rhatigan ◽

Vignesh Kumaravel ◽

Ciara Byrne ◽

...

Keyword(s):

Visible Light ◽

Visible Light Irradiation ◽

Density Functional ◽

Anatase Phase ◽

Sol Gel ◽

Chemical Properties ◽

Light Irradiation ◽

Health Concern ◽

Bacterial Inactivation ◽

X Ray

Indoor surface contamination by microbes is a major public health concern. A damp environment is one potential sources for microbe proliferation. Smart photocatalytic coatings on building surfaces using semiconductors like titania (TiO2) can effectively curb this growing threat. Metal-doped titania in anatase phase has been proved as a promising candidate for energy and environmental applications. In this present work, the antimicrobial efficacy of copper (Cu) doped TiO2 (Cu-TiO2) was evaluated against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) under visible light irradiation. Doping of a minute fraction of Cu (0.5 mol %) in TiO2 was carried out via sol-gel technique. Cu-TiO2 further calcined at various temperatures (in the range of 500 °C – 700 °C) to evaluate the thermal stability of TiO2 anatase phase. The physico-chemical properties of the samples were characterised through X-ray diffraction (XRD), Raman spectroscopy, X-ray photo-electron spectroscopy (XPS) and UV-visible spectroscopy techniques. XRD results revealed that the anatase phase of TiO2 was maintained well, up to 650 °C, by the Cu dopant. UV-DRS results suggested that the visible light absorption property of Cu-TiO2 was enhanced and the band gap is reduced to 2.8 eV. Density functional theory (DFT) studies emphasises the introduction of Cu+ and Cu2+ ions by replacing Ti4+ ions in the TiO2 lattice, creating oxygen vacancies. These further promoted the photocatalytic efficiency. A significantly high bacterial inactivation (99.9%) was attained in 30 mins of visible light irradiation by Cu-TiO2.

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Photocatalytic Degradation of Methylene Blue over Co-Ag3VO4 under Visible Light Irradiation

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.335-336.1385 ◽

2011 ◽

Vol 335-336 ◽

pp. 1385-1390 ◽

Cited By ~ 1

Author(s):

Shuo Wiei Zhao ◽

Hui Xu ◽

Hua Ming Li ◽

Yuan Guo Xu

Keyword(s):

Methylene Blue ◽

Photocatalytic Activity ◽

Visible Light ◽

Visible Light Irradiation ◽

Absorption Edge ◽

Diffuse Reflectance Spectroscopy ◽

Dye Degradation ◽

Light Irradiation ◽

Experimental Conditions ◽

X Ray

In order to improve the photocatalytic activity, Co was successfully loaded into Ag3VO4 by using impregnation process. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS) and diffuse reflectance spectroscopy (DRS). The XRD and SEM–EDS analyses revealed that Co ion was dispersed on Ag3VO4. The DRS results indicated that the absorption edge of the Co–Ag3VO4 catalyst shifted to longer wavelength. The enhanced photocatalytic activity of Co–Ag3VO4 for Methylene Blue(MB) dye degradation under visible light irradiation was due to its wider absorption edge and higher separation rate of photo-generated electron and holes. In the experimental conditions, it is demonstrated that the MB was effectively degraded by more than 95% within 40 min when the Co–Ag3VO4 catalyst was calcined at 300°C with 1 wt.% Co content.

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Fabrication of monoclinic BiVO4 photocatalyst film and its photocatalytic activity for organic pollutant removal

International Journal of Materials Research (formerly Zeitschrift fuer Metallkunde) ◽

10.1515/ijmr-2020-8065 ◽

2021 ◽

Vol 0 (0) ◽

Author(s):

Saranyoo Chaiwichian ◽

Buagun Samran

Keyword(s):

Visible Light ◽

Visible Light Irradiation ◽

Average Particle Size ◽

Pollutant Removal ◽

Light Irradiation ◽

Average Particle ◽

Film Sample ◽

Acid Orange 7 ◽

Acid Orange ◽

X Ray

Abstract Monoclinic BiVO4 photocatalyst films decorated on glass substrates were successfully fabricated via a dip-coating technique with different annealing temperatures of 400 °C, 450 °C, 500°C, and 550 °C. All of the physical and chemical properties of as-prepared BiVO4 photocatalyst film samples were investigated using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV–vis diffuse reflectance spectra techniques. The results revealed that the as-prepared BiVO4 photocatalyst film samples retained a monoclinic phase with an average particle size of about 50 – 100 nm. Moreover, the BiVO4 photocatalyst film samples showed a strong photoabsorption edge in the range of visible light with the band gap energy of 2.46 eV. The photocatalytic activities of all the film samples were tested by the degradation of model acid orange 7 under visible light irradiation. The BiVO4 photocatalyst film sample annealed at a temperature of 500 °C showed the highest photoactivity efficiency compared with other film samples, reaching up to 51%within 180 min. In addition, the stability and reusability of BiVO4 photocatalyst film sample made with an annealing temperature of 500 °C did not show loss of photodegradation efficiency of acid orange 7 after ten recycles. A likely mechanism of the photocatalytic process was established by trapping experiments, indicating that the hydroxyl radical scavenger species can be considered to play a key role for acid orange 7 degradation under visible light irradiation.

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Photocatalytic Activity of CuO/ZnO Heterostructure Nanocrystals under UV-Visible Light Irradiation

Materials Science Forum ◽

10.4028/www.scientific.net/msf.787.35 ◽

2014 ◽

Vol 787 ◽

pp. 35-40 ◽

Cited By ~ 2

Author(s):

Xiao Yan Zhou ◽

Peng Wei Zhou ◽

Hao Guo ◽

Bo Yang ◽

Ru Fei Ren

Keyword(s):

Photocatalytic Activity ◽

Visible Light ◽

Visible Light Irradiation ◽

Cuo Nanoparticles ◽

Light Irradiation ◽

Molar Ratio ◽

X Ray Diffraction ◽

X Ray ◽

Vis Spectroscopy ◽

Uv Visible

The p-n junction photocatalysts, p-CuO (at. 0-25%)/n-ZnO nanocomposite were prepared through hydrothermal method without using any organic solvent or surfactant. The as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-Ray spectroscopy, and UV-vis spectroscopy. The results demonstrated that the CuO/ZnO nanocomposite presented a two-dimensional morphology composed of sheet-like ZnO nanostructures adorned with CuO nanoparticles. The photocatalytic activity of CuO/ZnO with different Cu/Zn molar rations and pure ZnO synthesized by the identical synthetic route were evaluated by degrading methylene blue (MB) dye under UV-visible light irradiation. The CuO/ZnO with Cu/Zn molar ratio of 4% exhibits the highest photocatalytic activity compared that of the other photocatalysts under the identical conditions. It is mainly attributed to the increased charge separation rate in the nanocomposite and the extended photo-responding range.

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Cyclopentadienyl ruthenium complexes with tricarbollide ligands

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc2010057 ◽

2010 ◽

Vol 75 (11) ◽

pp. 1139-1148 ◽

Cited By ~ 10

Author(s):

Dmitry S. Perekalin ◽

Evgeniya A. Trifonova ◽

Ivan V. Glukhov ◽

Josef Holub ◽

Alexander R. Kudinov

Keyword(s):

Visible Light ◽

Visible Light Irradiation ◽

Ruthenium Complexes ◽

Light Irradiation ◽

X Ray Diffraction ◽

X Ray ◽

Ca 50

Reaction of the tricarbollide anion [7,8,9-C3B8H11]– (1a) with the naphthalene complex [CpRu(C10H8)]+ under visible light irradiation in CH2Cl2 gives the 12-vertex closo-ruthenacarborane 1-Cp-1,2,3,5-RuC3B8H11 (2; 87% yield). This complex was also obtained by reaction of 1a with CpRu(cod)Cl (97%). Upon heating at 80 °C in toluene 2 rearranges into isomer 1-Cp-1,2,4,10-RuC3B8H11 (3; 63%). Irradiation of 1a with [CpRu(C10H8)]+ in acetone gives the 11-vertex closo-1-Cp-1,2,3,4-RuC3B7H10 (4; 32%). The latter was also prepared by reaction of 1a with [CpRu(MeCN)3]+ (59%). Compound 2 slowly undergoes cage contraction in acetone giving 4. Irradiation of 1a with [Cp*Ru(C10H8)]+ affords the isomeric 12-vertex closo-ruthenacarboranes 1-Cp*-1,2,3,5-RuC3B8H11 and 1-Cp*-1,2,4,10-RuC3B8H11 (2.2:1 ratio; 56%). Reaction of the amino-substituted tricarbollide anion [7-tBuNH-7,8,9-C3B8H10]– with [(C5R5)Ru(C10H8)]+ (R = H, Me) selectively gives 12-vertex closo-ruthenacarboranes 1-(C5R5)-12-tBuNH-1,2,4,12-RuC3B8H10 (ca. 50%). The structures of 2 and 4 were confirmed by X-ray diffraction.

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Ag2O/ZnO Heterostructures with Enhanced Photocatalytic Activity

Materials Science Forum ◽

10.4028/www.scientific.net/msf.1035.1043 ◽

2021 ◽

Vol 1035 ◽

pp. 1043-1049

Author(s):

Di Xiang ◽

Chang Long Shao

Keyword(s):

Electron Microscopy ◽

Visible Light ◽

Visible Light Irradiation ◽

Environmental Remediation ◽

Organic Dyes ◽

Light Irradiation ◽

X Ray Diffraction ◽

X Ray ◽

Transmission Electron ◽

P Type

A simple route has been developed for the synthesis of Ag2O/ZnO heterostructures and the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS) and photoluminescence (PL) spectroscopy analysis. Considering the porous structure of Ag2O/ZnO, the photocatalytic degradation for the organic dyes, such as eosin red (ER), methyl orange (MO), methylene blue (MB) and rhodamine B (RhB), under visible light irradiation was investigated in detail. Noticeably, Ag2O/ZnO just took 40 min to degrade 96 % MB. The rate of degradation using the Ag2O/ZnO heterostructures was 2.3 times faster than that of the bare porous ZnO nanospheres under visible light irradiation due to that the recombination of the photogenerated charge was inhibited greatly in the p-type Ag2O and n-type ZnO semiconductor. So the Ag2O/ZnO heterostuctures showed the potential application on environmental remediation.

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Photocatalytic degradation of deoxynivalenol over dendritic-like α-Fe2O3 under visible light irradiation

Toxins ◽

10.3390/toxins11020105 ◽

2019 ◽

Vol 11 (2) ◽

pp. 105 ◽

Cited By ~ 14

Author(s):

Huiting Wang ◽

Jin Mao ◽

Zhaowei Zhang ◽

Qi Zhang ◽

Liangxiao Zhang ◽

...

Keyword(s):

Electron Microscopy ◽

Visible Light ◽

Photocatalytic Degradation ◽

Visible Light Irradiation ◽

Photoelectron Spectroscopy ◽

High Performance ◽

Synthesis Method ◽

Light Irradiation ◽

Trichothecene Mycotoxin ◽

X Ray

Deoxynivalenol (DON) is a secondary metabolite produced by Fusarium, which is a trichothecene mycotoxin. As the main mycotoxin with high toxicity, wheat, barley, corn and their products are susceptible to contamination of DON. Due to the stability of this mycotoxin, traditional methods for DON reduction often require a strong oxidant, high temperature and high pressure with more energy consumption. Therefore, exploring green, efficient and environmentally friendly ways to degrade or reduce DON is a meaningful and challenging issue. Herein, a dendritic-like α-Fe2O3 was successfully prepared using a facile hydrothermal synthesis method at 160 °C, which was systematically characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). It was found that dendritic-like α-Fe2O3 showed superior activity for the photocatalytic degradation of DON in aqueous solution under visible light irradiation (λ > 420 nm) and 90.3% DON (initial concentration of 4.0 μg/mL) could be reduced in 2 h. Most of all, the main possible intermediate products were proposed through high performance liquid chromatography-mass spectrometry (HPLC-MS) after the photocatalytic treatment. This work not only provides a green and promising way to mitigate mycotoxin contamination but also may present useful information for future studies.

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Photocatalytic Decomposition of Methylene Blue with Lanthanum Doping TiO2 under Visible Light Irradiation

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.734-737.2163 ◽

2013 ◽

Vol 734-737 ◽

pp. 2163-2167

Author(s):

Guang Xiu Cao ◽

Zhong Hou Zhang ◽

Bin Zhai

Keyword(s):

Methylene Blue ◽

Visible Light ◽

Visible Light Irradiation ◽

Photoelectron Spectroscopy ◽

Light Irradiation ◽

Photocatalytic Decomposition ◽

Lanthanum Doping ◽

X Ray ◽

Degradation Rates ◽

Vis Spectroscopy

Lanthanum doped TiO2 powders were prepared by hydrolysis of titanium tetra-n-butyl oxide and La (NO3)3 in solution. The resulting powders were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-Vis absorption spectroscopy. The photocatalytic activities of doped samples were evaluated by the decomposition of methylene blue under visible light irradiation. The XRD results showed that the doping of lanthanum could not only efficiently inhibit the grain growth but also suppress the phase transition of anatase to rutile. UV-Vis spectroscopy of lanthanum doping TiO2 indicated that the absorption onset red-shifted to the visible light region. XPS results revealed that La2O3 had formed which could enhance the surface area. The degradation rates of methylene blue verified that the visible light photocatalytic activity of TiO2 has been enhanced by the doping of lanthanum.

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Preparation and Characterizations of In0.1SnxZn0.85-2xS Powder Photocatalysts for Hydrogen Production under Visible Light Irradiation

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.364.238 ◽

2011 ◽

Vol 364 ◽

pp. 238-242 ◽

Cited By ~ 1

Author(s):

Kimi Melody ◽

Yuliati Leny ◽

Mustaffa Shamsuddin

Keyword(s):

Hydrogen Production ◽

Visible Light ◽

Solid Solutions ◽

Visible Light Irradiation ◽

Diffuse Reflectance ◽

Average Rate ◽

Light Irradiation ◽

X Ray Diffraction ◽

X Ray ◽

Uv Visible

A series of In0.1SnxZn0.85-2xS solid solutions was synthesized by hydrothermal method and employed as photocatalyst for photocatalytic hydrogen evolution under visible light irradiation. The structures, optical properties and morphologies of the solid solutions were studied by X-ray diffraction, diffuse reflectance UV–visible spectroscopy and field emission scanning electron microscopy. From the characterizations, it was confirmed that In0.1SnxZn0.85-2xS solid solution can be obtained and they have nanosized particles. The highest photocatalytic activity was observed on In0.1Sn0.03Zn0.79S photocatalyst, with average rate of hydrogen production 3.05 mmol/h, which was 1.2 times higher than the In0.1Zn0.85S photocatalyst.

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Photocatalytic properties of p-n heterojunction Ag2CO3/Ag3PO4/Ni thin films under visible light

Functional Materials Letters ◽

10.1142/s1793604719500851 ◽

2019 ◽

Vol 12 (06) ◽

pp. 1950085 ◽

Cited By ~ 1

Author(s):

Di Zhao ◽

Xuezheng An ◽

Yaxian Sun ◽

Guihua Li ◽

Hongyan Liu ◽

...

Keyword(s):

Thin Film ◽

Thin Films ◽

Visible Light ◽

Visible Light Irradiation ◽

Diffuse Reflectance ◽

Diffuse Reflectance Spectroscopy ◽

Light Irradiation ◽

X Ray Diffraction ◽

X Ray ◽

Photodegradation Efficiency

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.

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