Investigation of CO2 Adsorption on Triethylenetetramine Modified Adsorbents of TETA(n)/Zr-TSCD

In the present study, a new type of material of Zr-TSCD was first synthesized and modified with different amounts of triethylenetetramine (TETA). The properties of the adsorbents were characterised with X-ray diffraction, UV-vis diffuse reflectance spectroscopy, FT-IR spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, N2 adsorption–desorption, energy dispersion spectrum, and thermogravimetric analysis. The results suggested that Zr-TSCD (TSCD=Na3C6H5O7·2H2O) was successfully synthesized through the coordination of Zr atoms from ZrOCl2·8H2O and O species in –COO– groups. After functionalization with TETA, the structure of Zr-TSCD was preserved and the adsorption capacity of CO2 was enhanced dramatically. At 75°C, TETA(30)/Zr-TSCD achieved a maximum absorption capacity of 175.1mg g−1 in a stream of 10mL min−1 CO2. The adsorption capacity ratio of CO2/N2, CO2/O2, and CO2/SO2 was 10.5, 7.4, and 1.2, respectively. In addition, the adsorption capacity of CO2 remained stable during 10 adsorption–desorption cycles.

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Synthesis, Characterization, and Photocatalytic Evaluation of Manganese (III) Phthalocyanine Sensitized ZnWO4 (ZnWO4MnPc) for Bisphenol A Degradation under UV Irradiation

Nanomaterials ◽

10.3390/nano10112139 ◽

2020 ◽

Vol 10 (11) ◽

pp. 2139 ◽

Cited By ~ 1

Author(s):

Chukwuka Bethel Anucha ◽

Ilknur Altin ◽

Zekeriya Biyiklioglu ◽

Emin Bacaksiz ◽

Ismail Polat ◽

...

Keyword(s):

Bisphenol A ◽

Uv Irradiation ◽

Photoelectron Spectroscopy ◽

Photocatalytic Performance ◽

Diffuse Reflectance Spectroscopy ◽

Degradation Process ◽

X Ray Diffraction ◽

X Ray ◽

Uv Visible ◽

Adsorption Desorption

ZnWO4MnPc was synthesized via a hydrothermal autoclave method with 1 wt.% manganese (iii) phthalocyanine content. The material was characterized for its structural and morphological features via X-ray diffraction (XRD) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, transmission emission microscopy (TEM), scanning electron microscopy-Energy dispersive X-ray spectroscopy (SEM-EDX), N2 adsorption–desorption at 77K, X-ray photoelectron spectroscopy (XPS), and UV-visible/diffuse reflectance spectroscopy(UV-vis/DRS). ZnWO4MnPc photocatalytic performance was tested on the degradation of bisphenol A (BPA). The ZnWO4MnPc material removed 60% of BPA after 4 h of 365 nm UV irradiation. Degradation process improved significantly to about 80% removal in the presence of added 5 mM H2O2 after 4 h irradiation. Almost 100% removal was achieved after 30 min under 450 nm visible light irradiation in the presence of same concentration of H2O2. The effect of ions and humic acid (HA) towards BPA removal was also investigated.

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Preparation of GO/MIL-101(Fe,Cu) composite and its adsorption mechanisms for phosphate in aqueous solution

10.21203/rs.3.rs-191207/v1 ◽

2021 ◽

Author(s):

You Wu ◽

Zuannian Liu ◽

Bakhtari Mohammad Fahim ◽

Junnan Luo

Keyword(s):

Adsorption Capacity ◽

Photoelectron Spectroscopy ◽

Adsorption Mechanism ◽

Nitrogen Adsorption ◽

Adsorption Properties ◽

Maximum Adsorption Capacity ◽

X Ray Diffraction ◽

X Ray ◽

Adsorption Mechanisms ◽

Adsorption Desorption

Abstract In this study, MIL-101(Fe), MIL-101(Fe,Cu), and Graphene Oxide (GO) /MIL-101(Fe,Cu) were synthesized to compose a novel sorbent. The adsorption properties of these three MOFs-based composites were compared toward the removal of phosphate. Furthermore, the influencing factors including reaction time, pH, temperature and initial concentration on the adsorption capacity of phosphate on these materials as well as the reusability of the material were discussed. The structure of fabricated materials and the removal mechanism of phosphate on the composite material were analyzed by Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption-desorption analysis and zeta potential. The results show that the maximum adsorption capacity of phosphate by the composite GO/MIL-101(Fe,Cu)-2% was 204.60 mg·g− 1, which is higher than that of MIL-101(Fe,Cu) and MIL-101(Fe). likewise the specific surface area of GO/MIL-101(Fe,Cu)-2% is 778.11 m2/g is higher than that of MIL-101(Fe,Cu) and MIL-101(Fe),which are 747.75 and 510.66m2/g respectively. The adsorption mechanism of phosphate is electrostatic attraction, form coordination bonds and hydrogen bonds. The fabricated material is a promising adsorbent for the removal of phosphate with good reusability.

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Dye-Sensitized-Assisted, Enhanced Photocatalytic Activity of TiO2/Bi4V2O11

NANO ◽

10.1142/s1793292018500285 ◽

2018 ◽

Vol 13 (03) ◽

pp. 1850028 ◽

Cited By ~ 4

Author(s):

Mengjun Liang ◽

Zhiyuan Yang ◽

Ying Mei ◽

Haoran Zhou ◽

Shuijin Yang

Keyword(s):

Photocatalytic Activity ◽

Photoelectron Spectroscopy ◽

Diffuse Reflectance Spectroscopy ◽

X Ray Diffraction ◽

X Ray ◽

Dye Sensitized ◽

Transmission Electron ◽

Efficient Charge ◽

Degradation Activity ◽

Adsorption Desorption

In this study, the TiO2/Bi4V2O[Formula: see text] nanocomposite photocatalysts were prepared by loading different amount of TiO2 nanoparticles onto the surface of Bi4V2O[Formula: see text] nanospheres via a facile hydrothermal method. Afterwards, the as-synthesized samples were characterized by high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), N2 adsorption–desorption isotherms, X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS) and photocurrent techniques. The optimal TiO2/Bi4V2O[Formula: see text] composite with 20[Formula: see text]wt.% TiO2 loading (TB2) exhibited the best photocatalytic activity, which could degrade almost RhB completely within 30[Formula: see text]min under visible light irradiation. The enhanced photocatalytic activity of TiO2/Bi4V2O[Formula: see text] composites for RhB degradation could be mainly ascribed to the efficient charge separation over dye-induced sensitized and the increased specific surface area. Also, the photocatalytic activities of TiO2/Bi4V2O[Formula: see text] for CIP degradation were tested. After five consecutive recycling experiments, the photocatalytic degradation activity of TB2 could still reach 99% which indicated that the catalysts had superior stability. Based on the experimental and bandgap calculations, a possible photocatalytic mechanism of TiO2/Bi4V2O[Formula: see text] for RhB degradation was proposed.

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

Materials Express ◽

10.1166/mex.2021.1957 ◽

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.

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Hydrothermal Synthesis of Iodine-Doped Nanoplates with Enhanced Visible and Ultraviolet-Induced Photocatalytic Activities

International Journal of Photoenergy ◽

10.1155/2012/915386 ◽

2012 ◽

Vol 2012 ◽

pp. 1-12 ◽

Cited By ~ 5

Author(s):

Jiang Zhang ◽

Zheng-Hong Huang ◽

Yong Xu ◽

Feiyu Kang

Keyword(s):

Photocatalytic Activity ◽

Photoelectron Spectroscopy ◽

Oxygen Vacancies ◽

Diffuse Reflectance Spectroscopy ◽

Synergetic Effect ◽

X Ray Diffraction ◽

X Ray ◽

Selected Area Electron Diffraction ◽

Transmission Electron ◽

Photocatalytic Activities

The iodine-doped Bi2WO6(I-BWO) photocatalyst was prepared via a hydrothermal method using potassium iodide as the source of iodine. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM) and selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The photocatalytic activity of I-BWO for the degradation of rhodamine B (RhB) was higher than that of pure BWO and I2-BWO regardless of visible light (>420 nm) or ultraviolet light (<400 nm) irradiation. The results of DRS analysis showed that the I-BWO and I2-BWO catalysts had narrower band gaps. XPS analysis proved that the multivalent iodine species including I0and were coadsorbed on the defect surface of Bi2WO6in I-BWO. The enhanced PL intensity revealed that a large number of defects of oxygen vacancies were formed by the doping of iodine. The enhanced photocatalytic activity of I-BWO for degradation of RhB was caused by the synergetic effect of a small crystalline size, a narrow band gap, and plenty of oxygen vacancies.

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Bulk Versus Surface Modification of Alumina with Mn and Ce Based Oxides for CH4 Catalytic Combustion

Materials ◽

10.3390/ma12111771 ◽

2019 ◽

Vol 12 (11) ◽

pp. 1771 ◽

Cited By ~ 2

Author(s):

Stefan Neatu ◽

Mihaela M. Trandafir ◽

Adelina Stănoiu ◽

Ovidiu G. Florea ◽

Cristian E. Simion ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Catalytic Combustion ◽

Mixed Oxides ◽

Sol Gel ◽

Nitrogen Adsorption ◽

X Ray Diffraction ◽

X Ray ◽

Temperature Programmed ◽

Catalytic Combustion Of Methane ◽

Adsorption Desorption

This study presents the synthesis and characterization of lanthanum-modified alumina supported cerium–manganese mixed oxides, which were prepared by three different methods (coprecipitation, impregnation and citrate-based sol-gel method) followed by calcination at 500 °C. The physicochemical properties of the synthesized materials were investigated by various characterization techniques, namely: nitrogen adsorption-desorption isotherms, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and H2–temperature programmed reduction (TPR). This experimental study demonstrated that the role of the catalytic surface is much more important than the bulk one. Indeed, the incipient impregnation of CeO2–MnOx catalyst, supported on an optimized amount of 4 wt.% La2O3–Al2O3, provided the best results of the catalytic combustion of methane on our catalytic micro-convertors. This is mainly due to: (i) the highest pore size dimensions according to the Brunauer-Emmett-Teller (BET) investigations, (ii) the highest amount of Mn4+ or/and Ce4+ on the surface as revealed by XPS, (iii) the presence of a mixed phase (Ce2MnO6) as shown by X-ray diffraction; and (iv) a higher reducibility of Mn4+ or/and Ce4+ species as displayed by H2–TPR and therefore more reactive oxygen species.

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

Nanomaterials ◽

10.3390/nano9091341 ◽

2019 ◽

Vol 9 (9) ◽

pp. 1341 ◽

Cited By ~ 1

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.

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An Efficient Simple Hydrothermal Method to Synthesis FeS2 Microspheres and their Optical Property

Materials Science Forum ◽

10.4028/www.scientific.net/msf.847.72 ◽

2016 ◽

Vol 847 ◽

pp. 72-77

Author(s):

Yu Xuan Liang ◽

Peng Peng Bai ◽

Shu Qi Zheng

Keyword(s):

Photoelectron Spectroscopy ◽

Low Cost ◽

Wave Length ◽

Functional Materials ◽

Optical And Electrical Properties ◽

X Ray Diffraction ◽

Synthetic Sample ◽

X Ray ◽

New Type ◽

Good Uniformity

Pyrite (FeS2) is an important semiconductor material which shows various excellent optical and electrical properties and extensive applied prospect as a new-type, photoelectrical functional materials. In this study, a low cost and efficient simple hydrothermal two-step synthetic method was given to obtain FeS2 microspheres with 2-3 μm in diameter. The obtained products were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and ultraviolet and visible spectrophotometer (UV-Vis). XRD showed that the synthetic sample consisted of two crystal structures of FeS2, pyrite and marcasite. SEM observation indicated that FeS2 microspheres were well crystallized and had good uniformity. UV-Vis spectrum had a strong optical absorption in the region of 200-400 nm wave length. The reaction temperature had an impact on the size of FeS2 microspheres. A possible mechanism for the size of the FeS2 microspheres generated at high temperature is smaller than that at low temperature is discussed.

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Effect of cerium content on textural and hydrodesulfurization performance for dibenzothiophene over a bulk Ni2P catalyst

Progress in Reaction Kinetics and Mechanism ◽

10.1177/1468678319830798 ◽

2019 ◽

Vol 44 (1) ◽

pp. 37-44 ◽

Cited By ~ 1

Author(s):

Yunwu Yu ◽

Lianjie Liang ◽

Changwei Xu ◽

Yubo Dai ◽

Wenhao Pan ◽

...

Keyword(s):

Crystallite Size ◽

Photoelectron Spectroscopy ◽

Space Velocity ◽

X Ray Diffraction ◽

Reaction Conditions ◽

X Ray ◽

Weight Hourly Space Velocity ◽

Cerium Content ◽

Adsorption Desorption ◽

Hydrodesulfurization Activity

A series of ceria promoted Ni2P catalysts were prepared and evaluated in dibenzothiophene hydrodesulfurization steam. These catalysts were characterized by X-ray diffraction, N2 adsorption–desorption, CO chemisorptions, and X-ray photoelectron spectroscopy. The results showed that the addition of ceria into the bulk Ni2P catalyst was conducive to the formation of the Ni2P phase and contributed to a higher surface area, leading to a better dispersion and smaller crystallite size of Ni2P particles. The CexNi2P catalysts showed higher dibenzothiophene hydrodesulfurization activity than Ni2P catalyst and the Ce0.09Ni2P catalyst showed the highest dibenzothiophene hydrodesulfurization activity. The Ce0.09Ni2P catalyst showed a dibenzothiophene hydrodesulfurization conversion of 94.5% at the reaction conditions of 320°C, 4.0 MPa, a H2/oil ratio of 500 (V/V), and a weight hourly space velocity of 8.0 h−1. The dibenzothiophene was mainly transformed through desulfurization pathway.

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Enhanced Photocatalytic Activity of Titania by Co-Doping with Mo and W

Catalysts ◽

10.3390/catal8120631 ◽

2018 ◽

Vol 8 (12) ◽

pp. 631 ◽

Cited By ~ 16

Author(s):

Osmín Avilés-García ◽

Jaime Espino-Valencia ◽

Rubí Romero-Romero ◽

José Rico-Cerda ◽

Manuel Arroyo-Albiter ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Diffuse Reflectance Spectroscopy ◽

High Surface ◽

High Surface Area ◽

Absorption Capacity ◽

Radiation Absorption ◽

Experimental Conditions ◽

X Ray ◽

Assembly Method ◽

Co Doped

Various W and Mo co-doped titanium dioxide (TiO2) materials were obtained through the EISA (Evaporation-Induced Self-Assembly) method and then tested as photocatalysts in the degradation of 4-chlorophenol. The synthesized materials were characterized by thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectroscopy (RS), N2 physisorption, UV-vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The results showed that the W-Mo-TiO2 catalysts have a high surface area of about 191 m2/g, and the presence of an anatase crystalline phase. The co-doped materials exhibited smaller crystallite sizes than those with one dopant, since the crystallinity is inhibited by the presence of both species. In addition, tungsten and molybdenum dopants are distributed and are incorporated into the anatase structure of TiO2, due to changes in red parameters and lattice expansion. Under our experimental conditions, the co-doped TiO2 catalyst presented 46% more 4-chlorophenol degradation than Degussa P25. The incorporation of two dopant cations in titania improved its photocatalytic performance, which was attributed to a cooperative effect by decreasing the recombination of photogenerated charges, high radiation absorption capacity, high surface areas, and low crystallinity. When TiO2 is co-doped with the same amount of both cations (1 wt.%), the highest degradation and mineralization (97% and 74%, respectively) is achieved. Quinones were the main intermediates in the 4-chlorophenol oxidation by W-Mo-TiO2 and 1,2,4-benzenetriol was incompletely degraded.

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