scholarly journals Efficient degradation of picric acid using rGO-MnO2 hybrid nanocomposite under different light conditions

2021 ◽  
Vol 2070 (1) ◽  
pp. 012089
Author(s):  
B Usharani ◽  
V Manivannan ◽  
P Shanmugasundaram
Keyword(s):  
Photoelectron Spectroscopy ◽  
Uv Light ◽  
Picric Acid ◽  
Environmental Pollutant ◽  
Light Sources ◽  
Light Conditions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Light Medium

Abstract Picric acid is a very dangerous environmental pollutant generated from chemical and dye industries due to its high toxicity. Therefore, efforts have been made to develop techniques for the efficient degradation of picric acid. A novel rGO-MnO2 nanocomposite has been synthesized by chemical method for the degradation of picric acid in various light medium. The rGO-MnO2 nanocomposite was characterized by X-ray Photoelectron Spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Energy dispersive X-ray (EDAX), Ultraviolet-visible (UV-Vis) and Scanning electron microscope (SEM). The synthesized, pure rGO, MnO2 and rGO-MnO2 nanocomposite catalyst have been studied for the activity of photocatalytic degradation against picric acid under different light sources such as UV light (254,365,390 nm), visible light and sunlight. It is found that rGO-MnO2 has achieved better performance compared to that of pure rGO, MnO2.

scholarly journals Characterization of Tio2 And An As-Prepared Tio2/Sio2 Composite And Their Photocatalytic Performance For The Reduction Of Low-Concentration N-NO3- In Water

2021 ◽  
Author(s):  
Wanzhen Zhong ◽  
Weizhang Fu ◽  
Shujuan Sun ◽  
Lingsheng Wang ◽  
Huaihao Liu ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Uv Light ◽  
Removal Rate ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Load Rate ◽  
Hole Scavenger ◽  
Ft Ir

Abstract Excessive N-NO3- water pollution has become a widespread and serious problem that threatens human and ecosystem health. Here, a TiO2/SiO2 composite photocatalyst was prepared via the sol-gel/hydrothermal method. TiO2 and TiO2/SiO2 were characterized by X-ray diffraction (XRD), UV-Vis differential reflectance spectroscopy (DRS), Fourier infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). Afterward, the photocatalytic performance of TiO2 and TiO2/SiO2 to reduce low nitrate concentrations (30 mgN·L-1) under UV light were evaluated and the effects of different factors on this process were investigated, after which the reaction conditions were optimized. Removal rates of up to 99.93% were achieved at a hole scavenger (formic acid) concentration of 0.6 mL·L-1, a CO2 flow rate of 0.1 m3·h-1, and a TiO2 concentration of 0.9 g·L-1. In contrast, TiO2/SiO2 at a 1.4 g·L-1 concentration and a TiO2 load rate of 40% achieved a removal rate of 83.48%,But with more than 98% of nitrogen generation rate.NO2- and NH4+ were the minor products, whereas N2 was the main product.

scholarly journals Synthesis of Magnetic Ferrocene-Containing Polymer with Photothermal Effects for Rapid Degradation of Methylene Blue

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 558
Author(s):  
Wenhui Zhu ◽  
Caiyun Zhang ◽  
Yali Chen ◽  
Qiliang Deng
Keyword(s):  
Methylene Blue ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Degradation Rate ◽  
Model Compound ◽  
Vibrating Sample Magnetometer ◽  
Simulated Sunlight ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir

Photothermal materials are attracting more and more attention. In this research, we synthesized a ferrocene-containing polymer with magnetism and photothermal properties. The resulting polymer was characterized by Fourier-transform infrared (FT-IR), vibrating sample magnetometer (VSM), scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Its photo-thermocatalytic activity was investigated by choosing methylene blue (MB) as a model compound. The degradation percent of MB under an irradiated 808 nm laser reaches 99.5% within 15 min, and the degradation rate is 0.5517 min−1, which is 145 times more than that of room temperature degradation. Under irradiation with simulated sunlight, the degradation rate is 0.0092 min−1, which is approximately 2.5 times more than that of room temperature degradation. The present study may open up a feasible route to degrade organic pollutants.

ROOM TEMPERATURE PHOTOLUMINESCENCE OF POLYCRYSTALLINE SIC PREPARED FROM CARBON-SATURATED SI MELT

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1047-1051
Author(s):  
JIANPING MA ◽  
ZHIMING CHEN ◽  
GANG LU ◽  
MINGBIN YU ◽  
LIANMAO HANG ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Uv Light ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Composition And Structure ◽  
Light Excitation ◽  
Scanning Electron

Intense photoluminescence (PL) has been observed at room temperature from the polycrystalline SiC samples prepared from carbon-saturated Si melt at a temperature ranging from 1500 to 1650°C. Composition and structure of the samples have been confirmed by means of X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. PL measurements with 325 nm UV light excitation revealed that the room temperature PL spectrum of the samples consists of 3 luminescent bands, the peak energies of which are 2.38 eV, 2.77 eV and 3.06 eV, respectively. The 2.38 eV band is much stronger than the others. It is suggested that some extrinsic PL mechanisms associated with defect or interface states would be responsible to the intensive PL observed at room temperature.

scholarly journals Dual Light- and pH-Responsive Composite of Polyazo-Derivative Grafted Cellulose Nanocrystals

Materials ◽  
2018 ◽  
Vol 11 (9) ◽  
pp. 1725 ◽  
Author(s):  
Xiaohong Liu ◽  
Ming Li ◽  
Xuemei Zheng ◽  
Elias Retulainen ◽  
Shiyu Fu
Keyword(s):  
Cellulose Nanocrystals ◽  
Photoelectron Spectroscopy ◽  
Surface Composition ◽  
X Ray Diffraction ◽  
Responsive Materials ◽  
X Ray ◽  
Ph Response ◽  
Transmission Electron ◽  
Ft Ir ◽  
Hexyl Methacrylate

As a type of functional group, azo-derivatives are commonly used to synthesize responsive materials. Cellulose nanocrystals (CNCs), prepared by acid hydrolysis of cotton, were dewatered and reacted with 2-bromoisobuturyl bromide to form a macro-initiator, which grafted 6-[4-(4-methoxyphenyl-azo) phenoxy] hexyl methacrylate (MMAZO) via atom transfer radical polymerization. The successful grafting was supported by Fourier transform infrared spectroscopy (FT-IR) and Solid magnetic resonance carbon spectrum (MAS 13C-NMR). The morphology and surface composition of the poly{6-[4-(4-methoxyphenylazo) phenoxy] hexyl methacrylate} (PMMAZO)-grafted CNCs were confirmed with Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The grafting rate on the macro-initiator of CNCs was over 870%, and the polydispersities of branched polymers were narrow. The crystal structure of CNCs did not change after grafting, as determined by X-ray diffraction (XRD). The polymer PMMAZO improved the thermal stability of cellulose nanocrystals, as shown by thermogravimetry analysis (TGA). Then the PMMAZO-grafted CNCs were mixed with polyurethane and casted to form a composite film. The film showed a significant light and pH response, which may be suitable for visual acid-alkali measurement and reversible optical storage.

scholarly journals Preparation, Characterization, and Performance Analysis of S-Doped Bi2MoO6 Nanosheets

Nanomaterials ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 1341 ◽  
Author(s):  
Ruiqi Wang ◽  
Duanyang Li ◽  
Hailong Wang ◽  
Chenglun Liu ◽  
Longjun Xu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Degradation Rate ◽  
X Ray Diffraction ◽  
Photo Degradation ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir ◽  
And Performance ◽  
Adsorption Desorption ◽  
Excellent Stability

S-doped Bi2MoO6 nanosheets were successfully synthesized by a simple hydrothermal method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), N2 adsorption–desorption isotherms, Raman spectroscopy, Fourier transform infrared spectroscopy (FT-IR), elemental mapping spectroscopy, photoluminescence spectra (PL), X-ray photoelectron spectroscopy (XPS), and UV-visible diffused reflectance spectra (UV-vis DRS). The photo-electrochemical performance of the samples was investigated via an electrochemical workstation. The S-doped Bi2MoO6 nanosheets exhibited enhanced photocatalytic activity under visible light irradiation. The photo-degradation rate of Rhodamine B (RhB) by S-doped Bi2MoO6 (1 wt%) reached 97% after 60 min, which was higher than that of the pure Bi2MoO6 and other S-doped products. The degradation rate of the recovered S-doped Bi2MoO6 (1 wt%) was still nearly 90% in the third cycle, indicating an excellent stability of the catalyst. The radical-capture experiments confirmed that superoxide radicals (·O2−) and holes (h+) were the main active substances in the photocatalytic degradation of RhB by S-doped Bi2MoO6.

scholarly journals “PdO vs. PtO”—The Influence of PGM Oxide Promotion of Co3O4 Spinel on Direct NO Decomposition Activity

Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 62 ◽  
Author(s):  
Gunugunuri K. Reddy ◽  
Torin C. Peck ◽  
Charles A. Roberts
Keyword(s):  
Photoelectron Spectroscopy ◽  
No Decomposition ◽  
Single Element ◽  
X Ray Diffraction ◽  
X Ray ◽  
Promotional Effect ◽  
Ft Ir ◽  
Temperature Programmed ◽  
Thermal Stability Of

Direct decomposition of NO into N2 and O2 (2NO→N2 + O2) is recognized as the “ideal” reaction for NOx removal because it needs no reductant. It was reported that the spinel Co3O4 is one of the most active single-element oxide catalysts for NO decomposition at higher reaction temperatures, however, activity remains low below 650 °C. The present study aims to investigate new promoters for Co3O4, specifically PdO vs. PtO. Interestingly, the PdO promoter effect on Co3O4 was much greater than the PtO effect, yielding a 4 times higher activity for direct NO decomposition at 650 °C. Also, Co3O4 catalysts with the PdO promoter exhibit higher selectivity to N2 compared to PtO/Co3O4 catalysts. Several characterization measurements, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), H2-temperature programmed reduction (H2-TPR), and in situ FT-IR, were performed to understand the effect of PdO vs. PtO on the properties of Co3O4. Structural and surface analysis measurements show that impregnation of PdO on Co3O4 leads to a greater ease of reduction of the catalysts and an increased thermal stability of surface adsorbed NOx species, which contribute to promotion of direct NO decomposition activity. In contrast, rather than remaining solely as a surface species, PtO enters the Co3O4 structure, and it promotes neither redox properties nor NO adsorption properties of Co3O4, resulting in a diminished promotional effect compared to PdO.

scholarly journals Influence of Ionic Liquids Assisted Synthesis on Morphology and Photocatalytic Properties of Bi4O5Br2

Proceedings ◽  
2019 ◽  
Vol 16 (1) ◽  
pp. 26
Author(s):  
Patrycja Wilczewska ◽  
Aleksandra Bielicka-Giełdoń ◽  
Agnieszka Fiszka Borzyszkowska ◽  
Aleksandra Pieczyńska ◽  
Ewa Maria Siedlecka
Keyword(s):  
Ionic Liquids ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Properties ◽  
X Ray Diffraction ◽  
Sem Images ◽  
New Thought ◽  
X Ray ◽  
Chromium Vi ◽  
Ft Ir ◽  
Adsorption Desorption

A series of Bi4O5Br2 photocatalysts were prepared via an innovation method of synthesis with ionic liquids (ILs). The crystal structures were investigated by X-ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FT-IR). The Field Emission Scanning Electron Microscope (FE-SEM) images illustrated the unique structure of prepared photocatalysts. The photocatalysts were also characterized by N2 adsorption-desorption analysis, X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra (UV-vis/DRS) and photoluminescence spectra (PL). The role of ILs in synthesis of Bi4O5Br2 on morphology and photocatalytic properties were investigated. Rhodamine B, 5-fluorouracil and chromium (VI) were used as the model micropollutants to evaluated adsorption capacity, photooxidation and photoreduction ability of prepared Bi4O5Br2 under artificial solar light. This work provided a new thought for enhanced photocatalytic activity of bismuth oxybromide photocatalysts.

Preparation of N-doped TiO2 by oxidizing TiN and its application on phenol degradation

2013 ◽  
Vol 68 (4) ◽  
pp. 934-939 ◽  
Author(s):  
Ji-Guo Huang ◽  
Xiao-Guang Zhao ◽  
Meng-Yang Zheng ◽  
Sen Li ◽  
Yu Wang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Phenol Degradation ◽  
Light Sources ◽  
X Ray Diffraction ◽  
Simple Method ◽  
Doped Tio2 ◽  
X Ray ◽  
Nitrogen Doped ◽  
Different Temperatures

Incomplete oxidation of titanium nitride (TiN) to prepare nitrogen-doped TiO2 was verified by calcining TiN at different temperatures in air for 30 min. The as-prepared samples were characterized by X-ray diffraction, UV-Vis diffuse reflectance spectra and X-ray photoelectron spectroscopy. The results confirmed that oxidizing TiN incompletely is an effective and simple method to prepare nitrogen-doped TiO2. Photocatalytic degradation of phenol was conducted to evaluate the photocatalytic activity of as-prepared samples. The results showed that phenol can be degraded efficiently by the as-prepared samples under visible light; low phenol concentration was conducive to degradation; the optimum calcination temperature and photocatalyst dosage are 650 °C and 0.5 g/L, respectively. The effects of different light sources on phenol degradation were compared. The reusability of nitrogen-doped TiO2 was tested and the results indicated a relatively good reusability under laboratory conditions.

Green preparation of carbon dots for Hg2+ detection and cell imaging

2020 ◽  
Vol 10 (11) ◽  
pp. 1777-1787
Author(s):  
Yadian Xie ◽  
Shanshan Wang ◽  
Ning Fu ◽  
Yan Yang ◽  
Xingliang Liu ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Carbon Dots ◽  
High Sensitivity ◽  
Amorphous Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbon And Nitrogen ◽  
Transmission Electron ◽  
Sensitivity And Selectivity ◽  
Ft Ir

Carbon dots (CDs) also nitrogen-doped CDs (N-CDs) were produced by green hydrothermal synthesis using Pea and ethanediamine as the carbon and nitrogen source, separately. Transmission electron microscopy (TEM) images displayed that the prepared CDs and N-CDs were well dispersed, had a spherical morphology. X-ray diffraction (XRD) figures of CDs and N-CDs presented a graphitic amorphous structure. Fourier transform infrared spectroscopy (FT-IR) verified that CDs and N-CDs carried many different hydrophilic groups (for example hydroxyl, carboxyl/carbonyl, amide, amino groups) on the surface, X-ray photoelectron spectroscopy (XPS) together verified this result. However, the optical properties and fluorescence quantum yield for N-CDs were obviously superior to those of CDs. Furthermore, the prepared N-CDs displayed outstanding advantages including low toxicity, satisfactory biocompatibility, and excellent chemical stability. More prominently, the prepared N-CDs could detect Hg2+ ions with high sensitivity and selectivity in both water samples and HeLa cells.

ETHANOL SENSOR OF CdO/Al2O3/CeO2 OBTAINED FROM Ce-DOPED LAYERED DOUBLE HYDROXIDES WITH HIGH RESPONSE AND SELECTIVITY

2013 ◽  
Vol 06 (03) ◽  
pp. 1350035 ◽  
Author(s):  
DONGMEI XU ◽  
MEIYU GUAN ◽  
QINGHONG XU ◽  
YING GUO ◽  
YAO WANG
Keyword(s):  
Photoelectron Spectroscopy ◽  
Gas Sensing ◽  
X Ray Diffraction ◽  
X Ray ◽  
Composite Oxides ◽  
Structure Morphology ◽  
Ft Ir ◽  
Ethanol Sensing ◽  
Double Hydroxide ◽  
Double Hydroxides

In this paper, Ce -doped CdAl layered double hydroxide (LDH) was first synthesized and the derivative CdO/Al2O3/CeO2 composite oxide was prepared by calcining Ce -doped CdAl LDH. The structure, morphology and chemical state of the Ce doped CdAl LDH and CdO/Al2O3/CeO2 were also investigated by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), solid state nuclear magnetic resonance (SSNMR), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). The gas sensing properties of CdO/Al2O3/CeO2 to ethanol were further studied and compared with CdO/Al2O3 prepared from CdAl LDH, CeO2 powder as well as the calcined Ce salt. It turns out that CdO/Al2O3/CeO2 sensor shows best performance in ethanol response. Besides, CdO/Al2O3/CeO2 possesses short response/recovery time (12/72 s) as well as remarkable selectivity in ethanol sensing, which means composite oxides prepared from LDH are very promising in gas sensing application.

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