scholarly journals Preparation Method of Co3O4Nanoparticles Using Degreasing Cotton and Their Electrochemical Performances in Supercapacitors

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Hongyan Xu ◽  
Libo Gao ◽  
Qiang Zhang ◽  
Junyang Li ◽  
Jiangtao Diwu ◽  
...  

Co3O4nanoparticles were fabricated by a novel, facile, and environment-friendly carbon-assisted method using degreasing cotton. Structural and morphological characterizations were performed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The component of the sample obtained at different temperatures was measured by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Nitrogen adsorption and desorption isotherms were utilized to reveal the specific surface areas. The formation mechanism of Co3O4nanoparticles was also proposed, demonstrating that the additive degreasing cotton played an indispensable role in the process of synthesizing the sample. The resultant Co3O4sample calcined at 600°C exhibited superior electrochemical performance with better specific capacitance and long-term cycling life, due to its high specific surface areas and pores structures. Additionally, it has been proved that this facile synthetic strategy can be extended to produce other metal oxide materials (e.g., Fe3O4). As a consequence, the carbon-assisted method using degreasing cotton accompanied a promising prospect for practical application.

1985 ◽  
Vol 2 (4) ◽  
pp. 241-251 ◽  
Author(s):  
C. Martin ◽  
V. Rives

V2O5/TiO2 systems have been obtained by reacting TiO2 (P-25 from Degussa, ca 55% anatase, or a rutilised modification, ca 3% anatase) with gaseous VOCl3. The samples have been characterised by X-ray diffraction, UV–Vis spectrophotometry and nitrogen adsorption at 77 K. For the anatase carrier, a monolayer coverage of V2O5 is achieved, but only 0·46 monolayers are formed with the rutilised support. The specific surface areas decrease upon incorporation of V2O5, and that seems to be well dispersed without forming crystallites.


2008 ◽  
Vol 8 (12) ◽  
pp. 6437-6444 ◽  
Author(s):  
M. A. Albiter ◽  
R. Huirache-Acuña ◽  
F. Paraguay-Delgado ◽  
F. Zaera ◽  
G. Alonso-Núñez

In this study Co(Ni)/MoS2 unsupported nanocatalysts (nanorods and nanoribbons) were synthesized with Co(Ni)/(Co(Ni)+Mo)=0.3, 0.5 molar ratios for Co and Ni respectively. First the α-MoO3 nanostructures were impregnated with an aqueous solution of Co(Ni)Cl2·6H2O or Co(Ni)(NO3)2·6H2O, then were treated for 2 h at 473 K, and finally the precursors were activated under a H2S/H2 mixture (15% v/v H2S) by ramping the temperature from room temperature to 773 K and keeping it at that value for 2 h. The resulting materials were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, X-ray diffraction, specific surface area and X-ray photoelectron spectroscopy, and tested as catalysts for the hydrodesulfurization (HDS) of dibenzothiophene (DBT). It was found that these materials presented specific surface areas below 25 m2/g. The catalytic test showed that only when Co is added a promoter effect is observed compared with MoS2 unpromoted catalysts. Among the materials prepared, the Co/MoS2 catalyst made from cobalt chloride presented the highest catalytic activity (6.95 mol s−1 g−1catalyst) for the HDS of DBT. The selectivity for the latter indicated a clear preference for the direct desulphurization over the hydrogenating pathway.


2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
N. Cruz-González ◽  
O. Calzadilla ◽  
J. Roque ◽  
F. Chalé-Lara ◽  
J. K. Olarte ◽  
...  

In the last decade, the urgent need to environmental protection has promoted the development of new materials with potential applications to remediate air and polluted water. In this work, the effect of the TiO2 thin layer over MoS2 material in photocatalytic activity is reported. We prepared different heterostructures, using a combination of electrospinning, solvothermal, and spin-coating techniques. The properties of the samples were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray diffraction (XRD), nitrogen adsorption-desorption isotherms, UV-Vis diffuse reflectance spectroscopy (UV-Vis-DRS), and X-ray photoelectron spectroscopy (XPS). The adsorption and photocatalytic activity were evaluated by discoloration of rhodamine B solution. The TiO2-MoS2/TiO2 heterostructure presented three optical absorption edges at 1.3 eV, 2.28 eV, and 3.23 eV. The high adsorption capacity of MoS2 was eliminated with the addition of TiO2 thin film. The samples show high photocatalytic activity in the visible-IR light spectrum.


2011 ◽  
Vol 239-242 ◽  
pp. 3105-3108
Author(s):  
Ming Xian Liu ◽  
Li Hua Gan ◽  
Jun Hu ◽  
Hong Lai Liu ◽  
Long Wu Chen

In this paper, we present a novel approach for the synthesis of carbon microspheres via the polymerization of a high internal phase emulsion (HIPE). By using Span 80 and Tween 80 as emulsifiers, 1iquid paraffin as oil phase, and the mixture of resorcinol/formaldehyde (R/F) solution as aqueous phase, an O/W emulsion was obtained. This emulsion phase inverted to a W/O HIPE induced by ammonia which served as the polymerization catalyst. Carbon microspheres (CMs) were prepared by polymerization of the HIPE, followed by drying and carbonization. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Brunauer-Emmett-Teller (BET) analyzer were used to characterize as-prepared CMs. The results indicate that, in case of 0.25 wt% ammonia of the HIPE, the diameters of CMs decreased from about 2 to 1 μm when the mass fraction of aqueous R/F decreased from 0.714 to 0.357; the apparent density and the specific surface areas of the CMs, however, did not change obviously, which are about 0.6 g/cm3and 200 m2/g, respectively. The dosage of ammonia has a significant influence on the morphology and properties of CMs. With increasing of the ammonia mass to 1 wt% of the HIPE, the resultant carbon materials comprise not only CMs, but also some carbon sheets; the apparent density of which increased to 0.9 g/cm3and the specific surface areas of which decreased to below 100 m2/g. In addition, the other parameters for CMs preparation were also investigated. It was found that the proper conditions were controlling the temperature of 303-333 K and the oil/aqueous phase mass ratio of 2.5:7.


2020 ◽  
Vol 13 (02) ◽  
pp. 2051004
Author(s):  
Jinyan Xiong ◽  
Wei Li ◽  
Kai Zhao ◽  
Weijie Li ◽  
Gang Cheng

Nanocrystallite aggregates have great potential in semiconductor-based photocatalysis toward environmental pollution removal. In this work, we reported the fabrication of broccoli-like zinc oxide nanoaggregates in the presence of beta-cyclodextrin in ethylene glycol-H2O medium. The composition and structure of the as-obtained ZnO nanoaggregates were characterized by powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and nitrogen adsorption. It was observed that the beta-cyclodextrin played an important role in the fabrication of such broccoli-like structure. A plausible formation mechanism was discussed on the basis of the controllable experiments. The photocatalytic performance of the products was studied through the photodegradation of rhodamine B under simulated sunlight irradiation. Compared to the spherical ZnO nanoaggregates and ZnO broken spheres, the broccoli-like ZnO exhibited superior photocatalytic efficiency. Based on the photocurrent and electrochemical measurement results, the higher separation efficiency of the photogenerated carriers and lower recombination efficiency of the photoinduced electron–hole pairs over the broccoli-like ZnO nanoaggregates contributed to their remarkable photocatalytic activity.


NANO ◽  
2013 ◽  
Vol 08 (05) ◽  
pp. 1350050
Author(s):  
MIN GUAN ◽  
HAI-PENG BI ◽  
ZUYUAN WANG ◽  
SHAOHUA BU ◽  
LING HUANG ◽  
...  

Mesoporous silicas SBA-15 are modified with β-Cyclodextrins (β-CD) by simple grafting method. β-CD functionalized SBA-15 was characterized by Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), nitrogen adsorption–desorption measurements, thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS). Furthermore, the applicability of it is investigated through studying the adsorption properties of clenbuterol. It showed better adsorption capacities of clenbuterol than pure SBA-15. β-CD functionalized SBA-15 material has the potential applications in the treatment of clenbuterol contamination in food and environment science.


Processes ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 1925
Author(s):  
Tao Yu ◽  
Zhuo Chen ◽  
Yundong Wang ◽  
Jianhong Xu

H2S is a common but hazardous impurity in syngas, biogas, or natural gas. For some advanced power generation technologies, such as integrated gasification combined cycle (IGCC), solid oxide fuel cells, H2S content needs to be reduced to an acceptable level. In this work, a series of highly porous Zn-Cu and Zn-Co composites with three-dimensionally ordered macropores (3DOM) structure were synthesized via the colloidal crystal template method and used to remove H2S at 150 °C and one atm. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption studies, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) were carried out to analyze the fresh and spent adsorbents. The results show that all the adsorbents possess well-ordered macropores, a large surface area, and a highly dispersed active phase. The relative content of Zn and (Cu or Co) has a significant influence on the desulfurization performance of adsorbents. The addition of CuO significantly increases the sulfur capacity and 3DOM-Zn0.5Cu0.5 shows the largest sulfur capacity of all the adsorbents, reaching up to 102.5 mg/g. The multiple adsorption/regeneration cycles of 3DOM-Zn0.5Cu0.5 and 3DOM-Zn0.5Co0.5 indicate that the as-prepared adsorbents are stable, and the sulfur capacity can still exceed 65% of the fresh adsorbents after six cycles.


2002 ◽  
Vol 67 (7) ◽  
pp. 499-506 ◽  
Author(s):  
Marina Radojevic ◽  
Vidojko Jovic ◽  
Dragomir Karaulic ◽  
Dragomir Vitorovic

The changes in the pore structure and adsorption properties of sepiolite from Goles resulting from treatment with 4MHCl for various periods of time were investigated. The BET method specific surface areas, pore volumes and f ? plots were determined by nitrogen adsorption. The surface area progressively increased during the 70 hours of acid treatment, when a maximum was attained. The differences in the adsorption properties of the original and the acid treated sepiolite were evaluated by comparison of adsorption isotherms obtained with benzene, n-hexane, methanol and isooctane. The enhanced adsorption of isooctane was of great interest, since the sorption of this compound on natural sepiolites is generally very limited. The results suggest that chemical treatment of sepiolite with 4MHCl for 70 h produces an adsorbent of optimal porosity and other adsorption properties.


2020 ◽  
Vol 2020 ◽  
pp. 1-14 ◽  
Author(s):  
Nguyen Thi Lan ◽  
Vo Hoang Anh ◽  
Hoang Duc An ◽  
Nguyen Phi Hung ◽  
Dao Ngoc Nhiem ◽  
...  

In this study, C-N-S-tridoped TiO2 composite was fabricated from TiO2 prepared from ilmenite ore and thiourea by means of hydrothermal method. The obtained material was characterized by X-ray diffraction, Raman scattering spectroscopy, UV-Vis diffuse reflectance spectroscopy, nitrogen adsorption-desorption isotherms, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). It was found that C-N-S-tridoped TiO2 material has a large specific surface area, showing good photocatalytic activity on the degradation of antibiotic tetracycline in visible light region. The study on the mechanism of tetracycline photodegradation using the liquid chromatography with mass spectrometry was performed. It was found that tetracycline has been degraded over C-N-S-tridoped TiO2 catalyst into many different intermediates which can eventually be converted into CO2 and H2O. The kinetics of photocatalytic decomposition of tetracycline were investigated. In addition, the obtained material could catalyze well the degradation of other antibiotics (ciprofloxacin and chloramphenicol) and dyes (rhodamine-B, methylene blue, and organe red). The catalyst was stable after five recycles with slight loss of catalytic activity, which indicates great potential for practical application of C-N-S-tridoped TiO2 catalyst in treatment of wastewater containing tetracycline in particular or antibiotics in general.


Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1062 ◽  
Author(s):  
Yue Wang ◽  
Xiaoxiao Zhu ◽  
Dongqing Feng ◽  
Anthony K. Hodge ◽  
Liujiang Hu ◽  
...  

The Fenton-type oxidation catalyzed by iron minerals is a cost-efficient and environment-friendly technology for the degradation of organic pollutants in water, but their catalytic activity needs to be enhanced. In this work, a novel biochar-supported composite containing both iron sulfide and iron oxide was prepared, and used for catalytic degradation of the antibiotic ciprofloxacin through Fenton-type reactions. Dispersion of FeS/Fe3O4 nanoparticles was observed with scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS) and transmission electron microscopy (TEM). Formation of ferrous sulfide (FeS) and magnetite (Fe3O4) in the composite was validated by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Ciprofloxacin (initial concentration = 20 mg/L) was completely degraded within 45 min in the system catalyzed by this biochar-supported magnetic composite at a dosage of 1.0 g/L. Hydroxyl radicals (·OH) were proved to be the major reactive species contributing to the degradation reaction. The biochar increased the production of ·OH, but decreased the consumption of H2O2, and helped transform Fe3+ into Fe2+, according to the comparison studies using the unsupported FeS/Fe3O4 as the catalyst. All the three biochars prepared by pyrolysis at different temperatures (400, 500 and 600 °C) were capable for enhancing the reactivity of the iron compound catalyst.


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