SnO2/AgIO4 hybrids were fabricated by an in-situ synthetic method at room temperature. The structure, morphology, light response range, separation efficiency of the electron-hole pairs and elements of the as-synthesiz...SnO2/AgIO4 hybrids were fabricated by an in-situ synthetic method at room temperature. The structure, morphology, light response range, separation efficiency of the electron-hole pairs and elements of the as-synthesized samples were characterized by adopting X-ray diffraction, scanning electron microscopy, UV-Vis diffuse reflectance spectroscopy, electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy, respectively. The synergistically photocatalytic degradation mechanism of the as-synthesized composites was also proposed. The experimental results reveal that under the visible light irradiation the as-synthesized SnO2/AgIO4 hybrids can enhance the photocatalytic degradation efficiency of rhodamine B compared to pure samples. With increasing the molar ratios of AgIO4 to SnO2, it displays the trend of first increasing and then decreasing. When it is 1:2 in 150 min, the as-prepared hybrids have the highest degradation efficiency of 93.1%, which increases by 6550.0%, 30.5%, and 1505.0% compared to those of pure SnO2, AgIO4, and TiO2(P25), respectively. Moreover, the Sn-O-Ag cross-linking bonds are formed at the interfaces of SnO2 and AgIO4. In addition, superoxide anion radicals and holes play a major role in the process of photodegradation.展开更多
We investigated the removal of the organic dye rhodamine B in wastewater with recyclable AgBr/polypyrrole(PPy)nano-photocatalysts.With PPy as an active base for electron transfer,and hexadecyltrimethylammonium bromide...We investigated the removal of the organic dye rhodamine B in wastewater with recyclable AgBr/polypyrrole(PPy)nano-photocatalysts.With PPy as an active base for electron transfer,and hexadecyltrimethylammonium bromide(CTAB)as both the soft-templating agent and the bromine source,a series of AgBr/PPy nano-photocatalysts containing various proportions of silver were prepared in a convenient one-step synthesis procedure.The synthesized catalysts were characterized by TG analysis to reveal that,in comparison with pure PPy,the interaction between PPy and AgBr led to increased thermal stability.Chemical combination of PPy and AgBr was observed through XRD and XPS analyses.For the morphology study,the AgBr particles were found to be well dispersed in the PPy nanowire network from SEM results.In the photodegradation experiments,up to 92%rhodamine B was degraded by the AgBr/PPy catalysts in the period of 1 hour under 254 nm UV light.The catalysts could maintain 60%catalytic efficiency after 3 cycles in the recyclability test.展开更多
The present work deals on one hand with the valorization of wastes plastics, polyethylene terephthalate (PET) and Canarium schweinfurthii (CS) for the preparation of polyethylene terephthalate activated carbon (PETAC)...The present work deals on one hand with the valorization of wastes plastics, polyethylene terephthalate (PET) and Canarium schweinfurthii (CS) for the preparation of polyethylene terephthalate activated carbon (PETAC) and Canarium schweinfurthii/polyethylene terephthalate activated carbon (CS/PETAC). These adsorbents, on the other hand, were used for removal Rhodamine B (RhB) in an aqueous solution. PET and CS precursors were subjected to thermogravimetric analysis (TGA) and differential scanning colorimetry (DSC). Meanwhile PETAC and CS/PETAC were characterized using scanning electron microscopy-energy dispersive spectrometry (SEM-EDS), X-ray fluorescence (XRF), Fourier transformed infrared spectroscopy (FT-IR) and nitrogen adsorption/desorption (N<sub>2</sub>-BET). The N<sub>2</sub>-BET results revealed an increase of the specific surface area from 6.75 m<sup>2</sup>/g to 1282.0 m<sup>2</sup>/g for PETAC and CS/PETAC. The results of characterization indicated the key role played by plastic wastes to enhance the structural and functional properties of CS/PETAC. The RhB removal from the aqueous solution onto PETAC and CS/PETAC was found to be independent of pH, with an optimal contact time of RhB removal within 10 min for materials. The non-linear adsorption isotherm data for the adsorption process showed that the Langmuir and Freundlich models best fitted the RhB adsorption onto PETAC meanwhile only the Freundlich adsorption isotherm gave the best fit for CS/PETAC according to the correlation coefficient value closed to unity. The pseudo-first and pseudo-second-order kinetic models best described the RhB dye removal on both adsorbents. Additionally, the Elovich model confirmed that chemisorption was the main mechanism followed. These findings proved that CS seeds and PET wastes are low-cost precursors that should be given an added value by transforming them into an outstanding carbon material for dye removal in liquid effluent.展开更多
基金Funded by the Natural Science Foundation of Hebei Province,China(No.E2019210251)the National Natural Science Foundation of China(No.51778378)
文摘SnO2/AgIO4 hybrids were fabricated by an in-situ synthetic method at room temperature. The structure, morphology, light response range, separation efficiency of the electron-hole pairs and elements of the as-synthesized samples were characterized by adopting X-ray diffraction, scanning electron microscopy, UV-Vis diffuse reflectance spectroscopy, electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy, respectively. The synergistically photocatalytic degradation mechanism of the as-synthesized composites was also proposed. The experimental results reveal that under the visible light irradiation the as-synthesized SnO2/AgIO4 hybrids can enhance the photocatalytic degradation efficiency of rhodamine B compared to pure samples. With increasing the molar ratios of AgIO4 to SnO2, it displays the trend of first increasing and then decreasing. When it is 1:2 in 150 min, the as-prepared hybrids have the highest degradation efficiency of 93.1%, which increases by 6550.0%, 30.5%, and 1505.0% compared to those of pure SnO2, AgIO4, and TiO2(P25), respectively. Moreover, the Sn-O-Ag cross-linking bonds are formed at the interfaces of SnO2 and AgIO4. In addition, superoxide anion radicals and holes play a major role in the process of photodegradation.
基金Funded by Guizhou Provincial Natural Science Foundation(No.[2020]1Y030)Young Science and Technology Talents of Education Department of Guizhou Province(No.KY[2016]136)+1 种基金Doctoral Start-up Fund by Guizhou Normal University in 2014,The Guizhou Province Science and Technology Planning Project(No.[2016]1100)National Natural Science Foundation of China(No.21764004)。
文摘We investigated the removal of the organic dye rhodamine B in wastewater with recyclable AgBr/polypyrrole(PPy)nano-photocatalysts.With PPy as an active base for electron transfer,and hexadecyltrimethylammonium bromide(CTAB)as both the soft-templating agent and the bromine source,a series of AgBr/PPy nano-photocatalysts containing various proportions of silver were prepared in a convenient one-step synthesis procedure.The synthesized catalysts were characterized by TG analysis to reveal that,in comparison with pure PPy,the interaction between PPy and AgBr led to increased thermal stability.Chemical combination of PPy and AgBr was observed through XRD and XPS analyses.For the morphology study,the AgBr particles were found to be well dispersed in the PPy nanowire network from SEM results.In the photodegradation experiments,up to 92%rhodamine B was degraded by the AgBr/PPy catalysts in the period of 1 hour under 254 nm UV light.The catalysts could maintain 60%catalytic efficiency after 3 cycles in the recyclability test.
文摘The present work deals on one hand with the valorization of wastes plastics, polyethylene terephthalate (PET) and Canarium schweinfurthii (CS) for the preparation of polyethylene terephthalate activated carbon (PETAC) and Canarium schweinfurthii/polyethylene terephthalate activated carbon (CS/PETAC). These adsorbents, on the other hand, were used for removal Rhodamine B (RhB) in an aqueous solution. PET and CS precursors were subjected to thermogravimetric analysis (TGA) and differential scanning colorimetry (DSC). Meanwhile PETAC and CS/PETAC were characterized using scanning electron microscopy-energy dispersive spectrometry (SEM-EDS), X-ray fluorescence (XRF), Fourier transformed infrared spectroscopy (FT-IR) and nitrogen adsorption/desorption (N<sub>2</sub>-BET). The N<sub>2</sub>-BET results revealed an increase of the specific surface area from 6.75 m<sup>2</sup>/g to 1282.0 m<sup>2</sup>/g for PETAC and CS/PETAC. The results of characterization indicated the key role played by plastic wastes to enhance the structural and functional properties of CS/PETAC. The RhB removal from the aqueous solution onto PETAC and CS/PETAC was found to be independent of pH, with an optimal contact time of RhB removal within 10 min for materials. The non-linear adsorption isotherm data for the adsorption process showed that the Langmuir and Freundlich models best fitted the RhB adsorption onto PETAC meanwhile only the Freundlich adsorption isotherm gave the best fit for CS/PETAC according to the correlation coefficient value closed to unity. The pseudo-first and pseudo-second-order kinetic models best described the RhB dye removal on both adsorbents. Additionally, the Elovich model confirmed that chemisorption was the main mechanism followed. These findings proved that CS seeds and PET wastes are low-cost precursors that should be given an added value by transforming them into an outstanding carbon material for dye removal in liquid effluent.
