TiO2-coated carbon felt(TCF)composite catalysts have been prepared via a supercritical treatment of titanium tetraisopropoxide(TTIP)as the precursor.The physical properties of the catalysts were characterized by means...TiO2-coated carbon felt(TCF)composite catalysts have been prepared via a supercritical treatment of titanium tetraisopropoxide(TTIP)as the precursor.The physical properties of the catalysts were characterized by means of thermogravimetric and differential thermal analysis(TG–DTA),X-ray diffraction(XRD),fluorescence spectroscopy,scanning electron microscopy (SEM),and BET surface areas techniques.The photocatalytic activities of the materials were evaluated using the degradation of Congo red(CR)as a probe reaction.All the composites showed much higher photocatalytic activity than commercial P25 due to significant synergistic effects.Reused TCF retained high photocatalytic activity for degradation of CR.The photocatalytic efficiency in CR degradation was found to be strongly dependent on the TiO2-coating ratio and calcination temperature.A possible mechanism for the enhanced reactivity involves shuttling of electrons from TiO2 particles to the carbon felt(CF)as a result of an optimal arrangement in TCF that stabilizes charge separation and reduces charge recombination.In addition to the significant synergistic effects,the abundant spaces between adjacent carbon fibers allow UV light to penetrate into the felt-like photocatalyst to a considerable depth,so that a three-dimensional environment is available for the photocatalytic reaction.展开更多
A type of high visible-light active titanium oxinitride(TiO2-xNx) powder was prepared by a simple proc-ess:the calcination of the hydrated titanium dioxide at the atmosphere of ammonia-argon using a tu-bular electric ...A type of high visible-light active titanium oxinitride(TiO2-xNx) powder was prepared by a simple proc-ess:the calcination of the hydrated titanium dioxide at the atmosphere of ammonia-argon using a tu-bular electric furnace at high temperatures. The hydrated titanium dioxide was synthesized as the precursor of TiO2-xNx using titanic acid as raw material,which came from sulfate technique of produc-ing titanium white. The effects of temperature and reaction time on the nitrogen content,grain size and crystal structure were studied. The visible-light activity and photocatalysis capability of the powder were also investigated.展开更多
TiO2 is the most photoactive material because of its superstrong photooxidizing ability,and TiO2 photocatalysis has been widely applied in sustainable water treatment and environmental remediation.However,poor sunligh...TiO2 is the most photoactive material because of its superstrong photooxidizing ability,and TiO2 photocatalysis has been widely applied in sustainable water treatment and environmental remediation.However,poor sunlight or visible-light harvesting efficiency and fast recombination rate of the photogenerated charge carriers severely limit the practical applications of TiO2.To overcome these problems,the present work demonstrates a facile in-situ co-condensation method combined with hydrothermal treatment to prepare a series of graphitized carbon/TiO2 composite photocatalysts,and anatase TiO2 phase andp-p-conjugated polycyclic aromatic carbon structure are created simultaneously.As-prepared TiO2/C composites exhibit remarkably high visible-light photocatalytic activity in the degradation of aqueous emerging phenolic pollutants,acetaminophen(APAP)and methylparaben(MPB),and apparent rate constant of the TiO2/C composite with carbon doping level of 10.3%for APAP and MPB removal is 7.6 and 2.8 times higher than that of bare TiO2,and 6.2 and 2.6 times higher than that of Degussa P25 TiO2.Based on the results of photoelectrochemical experiments,indirect chemical probe measurements,and ESR spectroscopy,it is verified that doping TiO2 with graphitized carbon is responsible for this enhanced photocatalytic activity,which renders the improved visible-light harvesting ability,the accelerated separation of the photogenerated charge carriers,and enlarged BET surface areas.Through analyzing the intermediates yielded in the photodegradation process,the pathway of visible-light photocatalytic degradation of APAP and MPB over the TiO2/C composite is proposed.展开更多
Preparation of photocatalytic regenerationable activated carbon （AC） is the key step for the practical application of in situ regeneration of exhausted AC. A novel photocatalytic regenerationable AC was prepared by ...Preparation of photocatalytic regenerationable activated carbon （AC） is the key step for the practical application of in situ regeneration of exhausted AC. A novel photocatalytic regenerationable AC was prepared by sol-gel TiO2 in this work. The adsorption and regeneration performance of TiO2/AC were evaluated using phenol as model compound. Scanning electron microscope （SEM） and nitrogen （77 K） adsorption isotherm were used to determine the surface area, pore structure and the distribution of TiO2. The results showed that with the increase of TiO2 loading, adsorption capacity of TiO2/AC decreased and the regeneration efficiency increased. The photocatalytic regenerationable AC with suitable TiO2 loading （2 wt%） exhibited suitable adsorption capacity and regeneration efficiency. TiO2 located mainly in the entrance of macro-pore of carbon. The prepared TiO2/AC exhibited similar surface structure and pore structure with material carbon.展开更多
A batch fixed bed photoreactor,using felt-form activated carbon fibers(ACF)supported TiO2 photocatalyst(TiO2/ACF),was developed to carry out photocatalytic degradation of methylene blue(MB)solution.The effects of TiO2...A batch fixed bed photoreactor,using felt-form activated carbon fibers(ACF)supported TiO2 photocatalyst(TiO2/ACF),was developed to carry out photocatalytic degradation of methylene blue(MB)solution.The effects of TiO2 particle size,loaded TiO2 amount,initial MB concentration,airflow rate and successive run on the decomposition rate were investigated.The results showed that photodegradation process followed a pseudo-first-order reaction kinetic law.The apparent first-order reaction constant kapp was larger than 0.047 min- 1 with half reaction time t1/2 shorter than 15 min,which was comparable to reported data using suspended Degussa P-25 TiO2 particles.The high degradation rate was mainly attributed to adsorption of MB molecules onto the surface of TiO2/ACF.The photocatalytic efficiency still remained nearly 90%after 12 successive runs,showing that successive usage of the designed photoreactor was possible.The synergic enhancement effect in combination of adsorption with ACF and photodegradation with TiO2 was proved by comparing MB removal rates in the successive degradation and adsorption runs,respectively.展开更多
Applying quantitative temporal analysis of products reactor measurements, we studied the reactive removal of active oxygen present on Au/TiO2 catalysts after calcination at elevated temperatures （400 ＆#176;C） by CO...Applying quantitative temporal analysis of products reactor measurements, we studied the reactive removal of active oxygen present on Au/TiO2 catalysts after calcination at elevated temperatures （400 ＆#176;C） by CO pulses and its replenishment by O2 pulses at 80 ＆#176;C, focusing on the nature of the active oxygen species. In contrast to previous studies, which mainly focused on and clarified the nature of the active oxygen species for the catalytic CO oxidation, which is reversibly formed and replenished under typical reaction conditions, this study demonstrates that directly after calcina‐tion an additional oxygen species is present. This species is also active for the CO oxidation, but it is not or only very little formed under typical reaction conditions. Implications of these results on the mechanistic understanding of the CO oxidation on Au/TiO2, in particular on the role of different active oxygen species, will be discussed.展开更多
A commercially pure titanium sheet precipitated TiC in the surface layer was fabricated by anodic oxidation in NH4NO3 solution and heat treatment in air. The fabricated sheet showed relatively high photocatalytic acti...A commercially pure titanium sheet precipitated TiC in the surface layer was fabricated by anodic oxidation in NH4NO3 solution and heat treatment in air. The fabricated sheet showed relatively high photocatalytic activity in 0.1 M KI solution, which was close to the activity level of the P-25 particle made by Degussa Corporation. It exhibited photocatalytic activity in antifungal and antivirus tests under black light irradiation. The better photocatalytic activity under black light irradiation is considered to be related to the formation of anatase and rutile type titanium dioxides and rough surface. It also showed photocatalytic activity under visible light irradiation, which is considered to be attributable to carbon and nitrogen doping in titanium dioxide.展开更多
To tackle the crisis of global warming, it is imperative to control and mitigate the atmospheric carbon dioxide level. Photocatalytic reduction of carbon dioxide into solar fuels furnishes a gratifying solution to uti...To tackle the crisis of global warming, it is imperative to control and mitigate the atmospheric carbon dioxide level. Photocatalytic reduction of carbon dioxide into solar fuels furnishes a gratifying solution to utilize and reduce carbon dioxide emission and simultaneously generate renewable energy to sustain the societies. So far, titanium oxide-based semiconductors have been the most prevalently adopted catalysts in carbon dioxide photoreduction. This mini-review provides a general summary of the recent progresses in titanium oxide- catalyzed photocatalytic reduction of carbon dioxide. It first illustrates the use of structural engineering as a strategy to adjust and improve the catalytic performances. Then, it describes the introduction of one/two exogenous elements to modify the photocatalytic activity and/or selectivity. Lastly, it discusses multi-component hybrid titanium oxide composites.展开更多
基金supported by the Natural Science Foundation of Hunan Province (09JJ6101)the National Natural Science Foundation of China (50802034)
文摘TiO2-coated carbon felt(TCF)composite catalysts have been prepared via a supercritical treatment of titanium tetraisopropoxide(TTIP)as the precursor.The physical properties of the catalysts were characterized by means of thermogravimetric and differential thermal analysis(TG–DTA),X-ray diffraction(XRD),fluorescence spectroscopy,scanning electron microscopy (SEM),and BET surface areas techniques.The photocatalytic activities of the materials were evaluated using the degradation of Congo red(CR)as a probe reaction.All the composites showed much higher photocatalytic activity than commercial P25 due to significant synergistic effects.Reused TCF retained high photocatalytic activity for degradation of CR.The photocatalytic efficiency in CR degradation was found to be strongly dependent on the TiO2-coating ratio and calcination temperature.A possible mechanism for the enhanced reactivity involves shuttling of electrons from TiO2 particles to the carbon felt(CF)as a result of an optimal arrangement in TCF that stabilizes charge separation and reduces charge recombination.In addition to the significant synergistic effects,the abundant spaces between adjacent carbon fibers allow UV light to penetrate into the felt-like photocatalyst to a considerable depth,so that a three-dimensional environment is available for the photocatalytic reaction.
文摘A type of high visible-light active titanium oxinitride(TiO2-xNx) powder was prepared by a simple proc-ess:the calcination of the hydrated titanium dioxide at the atmosphere of ammonia-argon using a tu-bular electric furnace at high temperatures. The hydrated titanium dioxide was synthesized as the precursor of TiO2-xNx using titanic acid as raw material,which came from sulfate technique of produc-ing titanium white. The effects of temperature and reaction time on the nitrogen content,grain size and crystal structure were studied. The visible-light activity and photocatalysis capability of the powder were also investigated.
文摘TiO2 is the most photoactive material because of its superstrong photooxidizing ability,and TiO2 photocatalysis has been widely applied in sustainable water treatment and environmental remediation.However,poor sunlight or visible-light harvesting efficiency and fast recombination rate of the photogenerated charge carriers severely limit the practical applications of TiO2.To overcome these problems,the present work demonstrates a facile in-situ co-condensation method combined with hydrothermal treatment to prepare a series of graphitized carbon/TiO2 composite photocatalysts,and anatase TiO2 phase andp-p-conjugated polycyclic aromatic carbon structure are created simultaneously.As-prepared TiO2/C composites exhibit remarkably high visible-light photocatalytic activity in the degradation of aqueous emerging phenolic pollutants,acetaminophen(APAP)and methylparaben(MPB),and apparent rate constant of the TiO2/C composite with carbon doping level of 10.3%for APAP and MPB removal is 7.6 and 2.8 times higher than that of bare TiO2,and 6.2 and 2.6 times higher than that of Degussa P25 TiO2.Based on the results of photoelectrochemical experiments,indirect chemical probe measurements,and ESR spectroscopy,it is verified that doping TiO2 with graphitized carbon is responsible for this enhanced photocatalytic activity,which renders the improved visible-light harvesting ability,the accelerated separation of the photogenerated charge carriers,and enlarged BET surface areas.Through analyzing the intermediates yielded in the photodegradation process,the pathway of visible-light photocatalytic degradation of APAP and MPB over the TiO2/C composite is proposed.
基金The National Natural Science Foundation of China (No. 30400339) and the Heilongjiang Province Natural Science Foundation(No.C2004-29)
文摘Preparation of photocatalytic regenerationable activated carbon （AC） is the key step for the practical application of in situ regeneration of exhausted AC. A novel photocatalytic regenerationable AC was prepared by sol-gel TiO2 in this work. The adsorption and regeneration performance of TiO2/AC were evaluated using phenol as model compound. Scanning electron microscope （SEM） and nitrogen （77 K） adsorption isotherm were used to determine the surface area, pore structure and the distribution of TiO2. The results showed that with the increase of TiO2 loading, adsorption capacity of TiO2/AC decreased and the regeneration efficiency increased. The photocatalytic regenerationable AC with suitable TiO2 loading （2 wt%） exhibited suitable adsorption capacity and regeneration efficiency. TiO2 located mainly in the entrance of macro-pore of carbon. The prepared TiO2/AC exhibited similar surface structure and pore structure with material carbon.
基金Beijing Excellent Talents Training Fund(No.20061D0502200299)
文摘A batch fixed bed photoreactor,using felt-form activated carbon fibers(ACF)supported TiO2 photocatalyst(TiO2/ACF),was developed to carry out photocatalytic degradation of methylene blue(MB)solution.The effects of TiO2 particle size,loaded TiO2 amount,initial MB concentration,airflow rate and successive run on the decomposition rate were investigated.The results showed that photodegradation process followed a pseudo-first-order reaction kinetic law.The apparent first-order reaction constant kapp was larger than 0.047 min- 1 with half reaction time t1/2 shorter than 15 min,which was comparable to reported data using suspended Degussa P-25 TiO2 particles.The high degradation rate was mainly attributed to adsorption of MB molecules onto the surface of TiO2/ACF.The photocatalytic efficiency still remained nearly 90%after 12 successive runs,showing that successive usage of the designed photoreactor was possible.The synergic enhancement effect in combination of adsorption with ACF and photodegradation with TiO2 was proved by comparing MB removal rates in the successive degradation and adsorption runs,respectively.
文摘Applying quantitative temporal analysis of products reactor measurements, we studied the reactive removal of active oxygen present on Au/TiO2 catalysts after calcination at elevated temperatures （400 ＆#176;C） by CO pulses and its replenishment by O2 pulses at 80 ＆#176;C, focusing on the nature of the active oxygen species. In contrast to previous studies, which mainly focused on and clarified the nature of the active oxygen species for the catalytic CO oxidation, which is reversibly formed and replenished under typical reaction conditions, this study demonstrates that directly after calcina‐tion an additional oxygen species is present. This species is also active for the CO oxidation, but it is not or only very little formed under typical reaction conditions. Implications of these results on the mechanistic understanding of the CO oxidation on Au/TiO2, in particular on the role of different active oxygen species, will be discussed.
文摘A commercially pure titanium sheet precipitated TiC in the surface layer was fabricated by anodic oxidation in NH4NO3 solution and heat treatment in air. The fabricated sheet showed relatively high photocatalytic activity in 0.1 M KI solution, which was close to the activity level of the P-25 particle made by Degussa Corporation. It exhibited photocatalytic activity in antifungal and antivirus tests under black light irradiation. The better photocatalytic activity under black light irradiation is considered to be related to the formation of anatase and rutile type titanium dioxides and rough surface. It also showed photocatalytic activity under visible light irradiation, which is considered to be attributable to carbon and nitrogen doping in titanium dioxide.
基金the State Key Program of the National Natural Science Foundation of China (Grant Nos. 21436007 and 51472159).
文摘To tackle the crisis of global warming, it is imperative to control and mitigate the atmospheric carbon dioxide level. Photocatalytic reduction of carbon dioxide into solar fuels furnishes a gratifying solution to utilize and reduce carbon dioxide emission and simultaneously generate renewable energy to sustain the societies. So far, titanium oxide-based semiconductors have been the most prevalently adopted catalysts in carbon dioxide photoreduction. This mini-review provides a general summary of the recent progresses in titanium oxide- catalyzed photocatalytic reduction of carbon dioxide. It first illustrates the use of structural engineering as a strategy to adjust and improve the catalytic performances. Then, it describes the introduction of one/two exogenous elements to modify the photocatalytic activity and/or selectivity. Lastly, it discusses multi-component hybrid titanium oxide composites.
