scholarly journals Ultrasonically Induced Sulfur-Doped Carbon Nitride/Cobalt Ferrite Nanocomposite for Efficient Sonocatalytic Removal of Organic Dyes

Processes ◽  
2020 ◽  
Vol 8 (1) ◽  
pp. 104 ◽  
Author(s):  
Surabhi Kamal ◽  
Guan-Ting Pan ◽  
Siewhui Chong ◽  
Thomas Chung-Kuang Yang
Keyword(s):  
Methylene Blue ◽  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
Congo Red ◽  
Carbon Nitride ◽  
Cobalt Ferrite ◽  
Organic Dyes ◽  
Bandgap Energy ◽  
X Ray ◽  
Dye Pollutants

The sulfur-doped carbon nitride/cobalt ferrite nanocomposite (SCN/CoFe2O4) was prepared via ultrasonication and studied for the sonocatalytic degradation of wastewater organic dye pollutants including methylene blue, rhodamine B, and Congo red. The X-ray photoelectron spectroscopy confirmed the presence and atomic ratios of S, C, N, Co, Fe, and O elements and their corresponding bonds with Co2+ and Fe3+ cations. The nanocomposite was found to have aggregated nanoparticles on a sheet-like structure. The bandgap energy was estimated to be 1.85 eV. For the sonocatalytic degradation of 25-ppm methylene blue at 20 kHz, 1 W and 50% amplitude, the best operating condition was determined to be 1 g/L of catalyst dosage and 4 vol % of hydrogen peroxide loading. Under this condition, the sonocatalytic removal efficiency was the highest at 96% within a reaction period of 20 min. SCN/CoFe2O4 outperformed SCN and CoFe2O4 by 2.2 and 6.8 times, respectively. The SCN/CoFe2O4 nanocomposite was also found to have good reusability with a drop of only 7% after the fifth cycle. However, the degradation efficiencies were low when tested with rhodamine B and Congo red due to difference in dye sizes, structural compositions, and electric charges.

Preparation and application of two novel supramolecular polyoxmetalates with adsorption of organic contaminants in wastewater

2021 ◽  
Vol 20 (1) ◽  
pp. 69-79
Author(s):  
Wen-Hao Yang ◽  
Ying Pei ◽  
Hao-Yu Du ◽  
Shang-Hao Xiao ◽  
Xiu-Jun Wu ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Ir Spectra ◽  
Rhodamine B ◽  
Organic Contaminants ◽  
Organic Dyes ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
Adsorption Effect ◽  
X Ray ◽  
Elemental Analyses

Two new supramolecular polyoxmetalates were synthesized from 1, 4-bis[4-nitrile-pyridine)-N-methylene]phenyldibromide (L1) and 1, 2-bis[4-nitrile-pyridine)-N-methylene]phenyldibromide (L2) and (NH4)6Mo7–O24·4H2O under hydrothermal conditions. They are named p-[C20H18N2O4][Mo8O26] 0.5·H2O (1) and o-[C20H18N2O4][Mo8O26] ċ 0.5·H2O (2) respectively. The structures have been confirmed through single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectra. The adsorption test of compound 1 and compound 2 in organic dyes were carried out. It was found that compound 1 had a good adsorption effect on methylene blue (MB) and rhodamine B (RhB). The adsorption effect of compound 2 on MB is stronger than that of compound 1.

A novel ZrHIO6⋅4H2O catalyst for degradation of organic dyes at room temperature

2017 ◽  
Vol 10 (05) ◽  
pp. 1750055 ◽  
Author(s):  
Jiayin Li ◽  
Xinping Ma ◽  
Meifan Qian ◽  
Haoran Liu ◽  
Qiying Liu ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Organic Dyes ◽  
Dye Degradation ◽  
Light Illumination ◽  
X Ray ◽  
Dye Pollutants ◽  
Catalytic Role ◽  
Activity Loss ◽  
Aqueous Nitric Acid

It is interesting to obtain catalysts to degrade organic dye pollutants at room temperature for simultaneous purposes of environment-treating and energy-saving. In this work, a novel ZrHIO[Formula: see text]H2O catalyst was synthesized by reacting ZrO(NO[Formula: see text] with H5IO6 in aqueous nitric acid. The catalyst was found effective in degradation of rhodamine B (RhB) or methylene blue (MB) dyes at room temperature without light illumination. We used the ultraviolet–visible (UV–Vis) absorption spectra of dye solution as well as X-ray photoelectron spectroscopy (XPS) of ZrHIO[Formula: see text]H2O to confirm that the dye degradation was due to its catalytic role. Importantly, the ZrHIO[Formula: see text]H2O catalyst can be recycled five times without obvious activity loss and it achieved higher mineralization efficiency than the previously reported analogue in the degradation experiments.

Synthesis of coral-globular-like composite Ag/TiO2-SnO2 and its photocatalytic degradation of rhodamine B under multiple modes

2017 ◽  
Vol 76 (8) ◽  
pp. 2120-2132 ◽  
Author(s):  
Q. Song ◽  
L. Li ◽  
N. Zhuo ◽  
H. N. Zhang ◽  
X. Chen ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Organic Dyes ◽  
Uv Light ◽  
Sol Gel ◽  
X Ray ◽  
Tio2 Anatase

Taking cetyltrimethylammonium bromide (CTAB) as the template and using TiO2 as the substrate, coral-globular-like composite Ag/TiO2-SnO2 (CTAB) was successfully synthesized by the sol–gel combined with a temperature-programmed treatment method. X-ray diffraction, scanning electron microscopy (SEM), UV–vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, SEM combined with X-ray energy dispersive spectroscopy, and N2 adsorption–desorption tests were employed to characterize samples' crystalline phase, chemical composition, morphology and surface physicochemical properties. Results showed that composites not only had TiO2 anatase structure, but also had some generated SnTiO4, and the silver species was metallic Ag0. Ag/TiO2-SnO2 (CTAB) possessed a coral-globular-like structure with nanosheets in large quantities. The photocatalytic activity of Ag/TiO2-SnO2 (CTAB) had studied by degrading organic dyes under multi-modes, mainly using rhodamine B as the model molecule. Results showed that the coral-globular-like Ag/TiO2-SnO2 (CTAB) was higher photocatalytic activity than that of commercial TiO2, Ag/TiO2-SnO2, TiO2-SnO2 (CTAB), and TiO2-SnO2 under ultraviolet light irradiation. Moreover, Ag/TiO2-SnO2 (CTAB) composite can significantly affect the photocatalytic degradation under multi-modes including UV light, visible light, simulated solar light and microwave-assisted irradiation. Meanwhile, the photocatalytic activity of Ag/TiO2-SnO2 (CTAB) was maintained even after three cycles, indicating that the catalyst had good usability.

scholarly journals Efficient Adsorption of Methylene Blue by Porous Biochar Derived from Soybean Dreg Using a One-Pot Synthesis Method

Molecules ◽  
2021 ◽  
Vol 26 (3) ◽  
pp. 661
Author(s):  
Zhiwei Ying ◽  
Xinwei Chen ◽  
He Li ◽  
Xinqi Liu ◽  
Chi Zhang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Photoelectron Spectroscopy ◽  
Synthesis Method ◽  
Urban Pollution ◽  
Maximum Adsorption Capacity ◽  
One Pot ◽  
Average Pore ◽  
X Ray ◽  
Isotherm Equation

Soybean dreg is a by-product of soybean products production, with a large consumption in China. Low utilization value leads to random discarding, which is one of the important sources of urban pollution. In this work, porous biochar was synthesized using a one-pot method and potassium bicarbonate (KHCO3) with low-cost soybean dreg (SD) powder as the carbon precursor to investigating the adsorption of methylene blue (MB). The prepared samples were characterized with scanning electron microscopy (SEM), transmission electron microscopy (TEM), elemental analyzer (EA), Brunauer-Emmett-Teller (BET), X-ray diffractometer (XRD), Raman spectroscopy (Raman), Fourier transform infrared spectrometer (FTIR), and X-ray photoelectron spectroscopy (XPS). The obtained SDB-K-3 showed a high specific surface area of 1620 m2 g−1, a large pore volume of 0.7509 cm3 g−1, and an average pore diameter of 1.859 nm. The results indicated that the maximum adsorption capacity of SDB-K-3 to MB could reach 1273.51 mg g−1 at 318 K. The kinetic data were most consistent with the pseudo-second-order model and the adsorption behavior was more suitable for the Langmuir isotherm equation. This study demonstrated that the porous biochar adsorbent can be prepared from soybean dreg by high value utilization, and it could hold significant potential for dye wastewater treatment in the future.

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.

scholarly journals Low-Temperature Synthesis of Solution Processable Carbon Nitride Polymers

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1646
Author(s):  
Junyi Li ◽  
Neeta Karjule ◽  
Jiani Qin ◽  
Ying Wang ◽  
Jesús Barrio ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Carbon Nitride ◽  
Spatial Organization ◽  
Surface Display ◽  
Liquid Media ◽  
Low Temperature Synthesis ◽  
Temperature Synthesis ◽  
X Ray ◽  
N2 Atmosphere ◽  
Carbon Nitride Materials

Carbon nitride materials require high temperatures (>500 °C) for their preparation, which entails substantial energy consumption. Furthermore, the high reaction temperature limits the materials’ processability and the control over their elemental composition. Therefore, alternative synthetic pathways that operate under milder conditions are still very much sought after. In this work, we prepared semiconductive carbon nitride (CN) polymers at low temperatures (300 °C) by carrying out the thermal condensation of triaminopyrimidine and acetoguanamine under a N2 atmosphere. These molecules are isomers: they display the same chemical formula but a different spatial distribution of their elements. X-ray photoelectron spectroscopy (XPS) experiments and electrochemical and photophysical characterization confirm that the initial spatial organization strongly determines the chemical composition and electronic structure of the materials, which, thanks to the preservation of functional groups in their surface, display excellent processability in liquid media.

X-RAY PHOTOELECTRON SPECTROSCOPY STUDIES ON THE BONDING PROPERTIES OF AMORPHOUS CARBON NITRIDE FILMS SYNTHESIZED BY PULSED LASER DEPOSITION WITH DIFFERENT SUBSTRATE TEMPERATURES

2005 ◽  
Vol 12 (02) ◽  
pp. 185-195
Author(s):  
M. RUSOP ◽  
T. SOGA ◽  
T. JIMBO
Keyword(s):  
Pulsed Laser Deposition ◽  
Amorphous Carbon ◽  
Photoelectron Spectroscopy ◽  
Carbon Nitride ◽  
Measurement Techniques ◽  
Pulsed Laser ◽  
Laser Deposition ◽  
X Ray ◽  
Amorphous Carbon Nitride ◽  
Substrate Temperatures

Amorphous carbon nitride films ( a-CN x) were deposited by pulsed laser deposition of camphoric carbon target with different substrate temperatures (ST). The influence of ST on the synthesis of a-CN x films was investigated. The nitrogen-to-carbon (N/C) and oxygen-to-carbon (O/C) atomic ratios, bonding state, and microstructure of the deposited a-CN x films were characterized by X-ray photoelectron spectroscopy and were confirmed by other standard measurement techniques. The bonding states between C and N , and C and O in the deposited films were found to be significantly influenced by ST during the deposition process. The N/C and O/C atomic ratios of the a-CN x films reached the maximum value at 400°C. ST of 400°C was proposed to promote the desired sp 3-hybridized C and the C 3 N 4 phase. The C–N bonding of C–N , C=N and C≡N were observed in the films.

scholarly journals Decolorization of Methylene Blue by Ag/SrSnO3 Composites under Ultraviolet Radiation

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Patcharanan Junploy ◽  
Titipun Thongtem ◽  
Somchai Thongtem ◽  
Anukorn Phuruangrat
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Uv Radiation ◽  
Photoelectron Spectroscopy ◽  
Separation Process ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
X Ray ◽  
Negative Effect ◽  
Uv Visible

SrSn(OH)6 precursors synthesized by a cyclic microwave radiation (CMR) process were calcined at 900°C for 3 h to form rod-like SrSnO3. Further, the rod-like SrSnO3 and AgNO3 in ethylene glycol (EG) were ultrasonically vibrated to form rod-like Ag/SrSnO3 composites, characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron microscopy (EM), Fourier transform infrared (FTIR) spectroscopy, and UV-visible analysis. The photocatalyses of rod-like SrSnO3, 1 wt%, 5 wt%, and 10 wt% Ag/SrSnO3 composites were studied for degradation of methylene blue (MB, C16H18N3SCl) dye under ultraviolet (UV) radiation. In this research, the 5 wt% Ag/SrSnO3 composites showed the highest activity, enhanced by the electron-hole separation process. The photoactivity became lower by the excessive Ag nanoparticles due to the negative effect caused by reduction in the absorption of UV radiation.

FeYO3@rGO nanocomposites: Synthesis, characterization and application in photooxidative degradation of atrazine under visible light

2021 ◽  
Vol 11 (5) ◽  
pp. 706-716
Author(s):  
Nada D. Al-Khthami ◽  
Tariq Altalhi ◽  
Mohammed Alsawat ◽  
Mohamed S. Amin ◽  
Yousef G. Alghamdi ◽  
...  
Keyword(s):  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Bandgap Energy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Structural Surface ◽  
Adsorption Desorption

Different organic pollutants have been remediated photo catalytically by applying perovskite photocatalysts. Atrazine (ATR) is a pesticide commonly detected as a pollutant in drinking, surface and ground water. Herein, FeYO3@rGO heterojunction was synthesized and applied for photooxidation decomposition of ATR. First, FeYO 3nanoparticles (NPs) were prepared via routine sol-gel. After that, FeYO3 NPs were successfully incorporated with different percentages (5, 10, 15 and 20 wt.%) of reduced graphene oxide (rGO) in the synthesis of novel FeYO3@rGO photocatalyst. Morphological, structural, surface, optoelectrical and optical characteristics of constructed materials were identified via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), adsorption/desorption isotherms, diffusive reflectance (DR) spectra, and photoluminescence response (PL). Furthermore, photocatalytic achievement of the constructed materials was evaluated via photooxidative degradation of ATR. Various investigations affirmed the usefulness of rGO incorporation on the advancement of formed photocatalysts. Actually, novel nanocomposite containing rGO (15 wt.%) possessed diminished bandgap energy, as well as magnified visible light absorption. Furthermore, such nanocomposite presented exceptional photocatalytic achievement when exposed to visible light as ATR was perfectly photooxidized over finite amount (1.6 g · L-1) from the optimized photocatalyst when illuminated for 30 min. The advanced photocatalytic performance of constructed heterojunctions could be accredited mainly to depressed recombination amid induced charges. The constructed FeYO3@rGO nanocomposite is labelled as efficient photocatalyst for remediation of herbicides from aquatic environments.

scholarly journals Facile Preparation of Rod-like MnO Nanomixtures via Hydrothermal Approach and Highly Efficient Removal of Methylene Blue for Wastewater Treatment

Nanomaterials ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 10 ◽  
Author(s):  
Yuelong Xu ◽  
Bin Ren ◽  
Ran Wang ◽  
Lihui Zhang ◽  
Tifeng Jiao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Photoelectron Spectroscopy ◽  
Degradation Mechanism ◽  
Dye Adsorption ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Transmission Electron ◽  
Degradation Ratio ◽  
Hydrothermal Approach

In the present study, nanoscale rod-shaped manganese oxide (MnO) mixtures were successfully prepared from graphitic carbon nitride (C3N4) and potassium permanganate (KMnO4) through a hydrothermal method. The as-prepared MnO nanomixtures exhibited high activity in the adsorption and degradation of methylene blue (MB). The as-synthesized products were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), surface area analysis, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Furthermore, the effects of the dose of MnO nanomixtures, pH of the solution, initial concentration of MB, and the temperature of MB removal in dye adsorption and degradation experiments was investigated. The degradation mechanism of MB upon treatment with MnO nanomixtures and H2O2 was studied and discussed. The results showed that a maximum adsorption capacity of 154 mg g−1 was obtained for a 60 mg L−1 MB solution at pH 9.0 and 25 °C, and the highest MB degradation ratio reached 99.8% under the following optimum conditions: 50 mL of MB solution (20 mg L−1) at room temperature and pH ≈ 8.0 with 7 mg of C, N-doped MnO and 0.5 mL of H2O2.

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