WorldWideScience

Sample records for tio2-nanotube-array-based photocatalytic fuel

  1. Continuous photocatalytic fuel production over wide-bandgap metal oxides

    OpenAIRE

    Bazzo, Antonio

    2014-01-01

    Artificial photosynthesis has been proposed as one of the possible solutions to the energetic and chemical-feedstock problems to cope with the anticipated near future depletion of fossil fuel resources. This doctoral thesis deals with the study of promising catalysts and reactor designs to enhance the reaction efficiency and understand the origin of photocatalytic activity. A continuous flow reaction system was designed and constructed to study CO2 photoreduction with H2O and photocatalytic w...

  2. Understanding metal–organic frameworks for photocatalytic solar fuel production

    NARCIS (Netherlands)

    Garcia Santaclara, J.; Kapteijn, F.; Gascon Sabate, J.; van der Veen, M.A.

    The fascinating chemical and physical properties of MOFs have recently stimulated exploration of their application for photocatalysis. Despite the intense research effort, the efficiency of most photocatalytic MOFs for solar fuel generation is still very modest. In this highlight we analyse the

  3. Understanding metal-organic frameworks for photocatalytic solar fuel production

    NARCIS (Netherlands)

    Garcia Santaclara, J.

    2017-01-01

    The fascinating chemical and physical properties of MOFs have recently stimulated exploration of their application for photocatalysis. Despite the intense research effort, the efficiencies of most photocatalytic MOFs for solar fuel generation are still very modest. In this introduction we analyse

  4. Role of dissolved oxygen on the degradation mechanism of Reactive Green 19 and electricity generation in photocatalytic fuel cell.

    Science.gov (United States)

    Lee, Sin-Li; Ho, Li-Ngee; Ong, Soon-An; Wong, Yee-Shian; Voon, Chun-Hong; Khalik, Wan Fadhilah; Yusoff, Nik Athirah; Nordin, Noradiba

    2018-03-01

    In this study, a membraneless photocatalytic fuel cell with zinc oxide loaded carbon photoanode and platinum loaded carbon cathode was constructed to investigate the impact of dissolved oxygen on the mechanism of dye degradation and electricity generation of photocatalytic fuel cell. The photocatalytic fuel cell with high and low aeration rate, no aeration and nitrogen purged were investigated, respectively. The degradation rate of diazo dye Reactive Green 19 and the electricity generation was enhanced in photocatalytic fuel cell with higher dissolved oxygen concentration. However, the photocatalytic fuel cell was still able to perform 37% of decolorization in a slow rate (k = 0.033 h -1 ) under extremely low dissolved oxygen concentration (approximately 0.2 mg L -1 ) when nitrogen gas was introduced into the fuel cell throughout the 8 h. However, the change of the UV-Vis spectrum indicates that the intermediates of the dye could not be mineralized under insufficient dissolved oxygen level. In the aspect of electricity generation, the maximum short circuit current (0.0041 mA cm -2 ) and power density (0.00028 mW cm -2 ) of the air purged photocatalytic fuel cell was obviously higher than that with nitrogen purging (0.0015 mA cm -2 and 0.00008 mW cm -2 ). Copyright © 2017 Elsevier Ltd. All rights reserved.

  5. Conversion of carbohydrate into hydrogen fuel by a photocatalytic process

    Energy Technology Data Exchange (ETDEWEB)

    Kawai, T; Sakata, T

    1980-01-01

    The conversion of carbohydrates into H by a photocatalytic process is described. Powders of RuO/sub 2/, TiO/sub 2/, and Pt (weight ratio 10:100:5) were dissolved in H/sub 2/O containing sugar, starch, or cellulose and irradiated with UV. The cellulose reaction was also performed in 6M NaOH. The RuO/sub 2/-TiO/sub 2/-Pt powder acts as an electrochemical microcell; light of energy larger than the band gap of TiO/sub 2/ produces electron-hole pairs which separate and produce redox reactions at the particle-solution interface. The gases evolved using H/sub 2/O were mainly H and CO/sub 2/. H and Na/sub 2/CO/sub 3/ or NaHCO/sub 3/ were produced on irradiation of the NaOH solution at increased rates with respect to reactions in water.

  6. Photocatalytic conversion of CO2 into value-added and renewable fuels

    International Nuclear Information System (INIS)

    Yuan, Lan; Xu, Yi-Jun

    2015-01-01

    Graphical abstract: Artificial photosynthesis that uses solar light energy to convert CO 2 to form value-added and renewable fuels is considered to be a promising avenue to solve the problems relating to CO 2 . However, the state-of-the-art photocatalytic efficiency of CO 2 reduction is far from being optimal as a viable economical process. The present review is mainly focused on the progress made in exploring more efficient photocatalysts for CO 2 photoreduction and the undergoing mechanisms, which is anticipated to contribute to further advancement in CO 2 photoreduction with on-going efforts. - Highlights: • Brief introduction about the basic principle of artificial photosynthesis of CO 2 . • Progress made in exploring more efficient photocatalysts for CO 2 reduction. • Efforts devoted to excavate the in-depth mechanism of CO 2 photoreduction. • Perspectives on future research directions and open issues in CO 2 photoreduction. - Abstract: The increasing energy crisis and the worsening global climate caused by the excessive utilization of fossil fuel have boosted tremendous research activities about CO 2 capture, storage and utilization. Artificial photosynthesis that uses solar light energy to convert CO 2 to form value-added and renewable fuels such as methane or methanol has been consistently drawing increasing attention. It is like killing two birds with one stone since it can not only reduce the greenhouse effects caused by CO 2 emission but also produce value added chemicals for alternative energy supplying. This review provides a brief introduction about the basic principles of artificial photosynthesis of CO 2 and the progress made in exploring more efficient photocatalysts from the viewpoint of light harvesting and photogenerated charge carriers boosting. Moreover, the undergoing mechanisms of CO 2 photoreduction are discussed with selected examples, in terms of adsorption of reactants, CO 2 activation as well as the possible reaction pathways

  7. Converting hazardous organics into clean energy using a solar responsive dual photoelectrode photocatalytic fuel cell.

    Science.gov (United States)

    Li, Jianyong; Li, Jinhua; Chen, Quanpeng; Bai, Jing; Zhou, Baoxue

    2013-11-15

    Direct discharging great quantities of organics into water-body not only causes serious environmental pollution but also wastes energy sources. In this paper, a solar responsive dual photoelectrode photocatalytic fuel cell (PFC(2)) based on TiO2/Ti photoanode and Cu2O/Cu photocathode was designed for hazardous organics treatment with simultaneous electricity generation. Under solar irradiation, the interior bias voltage produced for the Fermi level difference between photoelectrodes drives photoelectrons of TiO2/Ti photoanode to combine with photoholes of Cu2O/Cu photocathode through external circuit thus generating electricity. In the meantime, organics are decomposed by photoholes remained at TiO2/Ti photoanode. By using various hazardous organics including azo dyes as model pollutants, the PFC showed high converting performance of organics into electricity. For example, in 0.05 M phenol solution, a short-circuit current density 0.23 mA cm(-2), open-circuit voltage 0.49 V, maximum power output 0.3610(-4)W cm(-2) was achieved. On the other hand, removal rate of chroma reached 67%, 87% and 63% in 8h for methyl orange, methylene blue, Congo red, respectively. Copyright © 2013 Elsevier B.V. All rights reserved.

  8. Photocatalytic conversion of CO{sub 2} into value-added and renewable fuels

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Lan [State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou 350002 (China); College of Chemistry, New Campus, Fuzhou University, Fuzhou 350108 (China); Xu, Yi-Jun, E-mail: yjxu@fzu.edu.cn [State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou 350002 (China); College of Chemistry, New Campus, Fuzhou University, Fuzhou 350108 (China)

    2015-07-01

    Graphical abstract: Artificial photosynthesis that uses solar light energy to convert CO{sub 2} to form value-added and renewable fuels is considered to be a promising avenue to solve the problems relating to CO{sub 2}. However, the state-of-the-art photocatalytic efficiency of CO{sub 2} reduction is far from being optimal as a viable economical process. The present review is mainly focused on the progress made in exploring more efficient photocatalysts for CO{sub 2} photoreduction and the undergoing mechanisms, which is anticipated to contribute to further advancement in CO{sub 2} photoreduction with on-going efforts. - Highlights: • Brief introduction about the basic principle of artificial photosynthesis of CO{sub 2}. • Progress made in exploring more efficient photocatalysts for CO{sub 2} reduction. • Efforts devoted to excavate the in-depth mechanism of CO{sub 2} photoreduction. • Perspectives on future research directions and open issues in CO{sub 2} photoreduction. - Abstract: The increasing energy crisis and the worsening global climate caused by the excessive utilization of fossil fuel have boosted tremendous research activities about CO{sub 2} capture, storage and utilization. Artificial photosynthesis that uses solar light energy to convert CO{sub 2} to form value-added and renewable fuels such as methane or methanol has been consistently drawing increasing attention. It is like killing two birds with one stone since it can not only reduce the greenhouse effects caused by CO{sub 2} emission but also produce value added chemicals for alternative energy supplying. This review provides a brief introduction about the basic principles of artificial photosynthesis of CO{sub 2} and the progress made in exploring more efficient photocatalysts from the viewpoint of light harvesting and photogenerated charge carriers boosting. Moreover, the undergoing mechanisms of CO{sub 2} photoreduction are discussed with selected examples, in terms of adsorption of

  9. Highly efficient visible light photocatalytic reduction of CO2 to hydrocarbon fuels by Cu-nanoparticle decorated graphene oxide.

    Science.gov (United States)

    Shown, Indrajit; Hsu, Hsin-Cheng; Chang, Yu-Chung; Lin, Chang-Hui; Roy, Pradip Kumar; Ganguly, Abhijit; Wang, Chen-Hao; Chang, Jan-Kai; Wu, Chih-I; Chen, Li-Chyong; Chen, Kuei-Hsien

    2014-11-12

    The production of renewable solar fuel through CO2 photoreduction, namely artificial photosynthesis, has gained tremendous attention in recent times due to the limited availability of fossil-fuel resources and global climate change caused by rising anthropogenic CO2 in the atmosphere. In this study, graphene oxide (GO) decorated with copper nanoparticles (Cu-NPs), hereafter referred to as Cu/GO, has been used to enhance photocatalytic CO2 reduction under visible-light. A rapid one-pot microwave process was used to prepare the Cu/GO hybrids with various Cu contents. The attributes of metallic copper nanoparticles (∼4-5 nm in size) in the GO hybrid are shown to significantly enhance the photocatalytic activity of GO, primarily through the suppression of electron-hole pair recombination, further reduction of GO's bandgap, and modification of its work function. X-ray photoemission spectroscopy studies indicate a charge transfer from GO to Cu. A strong interaction is observed between the metal content of the Cu/GO hybrids and the rates of formation and selectivity of the products. A factor of greater than 60 times enhancement in CO2 to fuel catalytic efficiency has been demonstrated using Cu/GO-2 (10 wt % Cu) compared with that using pristine GO.

  10. Photocatalytic reduction of CO2 into hydrocarbon solar fuels over g-C3N4-Pt nanocomposite photocatalysts.

    Science.gov (United States)

    Yu, Jiaguo; Wang, Ke; Xiao, Wei; Cheng, Bei

    2014-06-21

    Photocatalytic reduction of CO2 into renewable hydrocarbon fuels is an alternative way to develop reproducible energy, which is also a promising way to solve the problem of the greenhouse effect. In this work, graphitic carbon nitride (g-C3N4) was synthesized by directly heating thiourea at 550 °C and then a certain amount of Pt was deposited on it to form g-C3N4-Pt nanocomposites used as catalysts for photocatalytic reduction of CO2 under simulated solar irradiation. The main products of photocatalysis were CH4, CH3OH and HCHO. The deposited Pt acted as an effective cocatalyst, which not only influenced the selectivity of the product generation, but also affected the activity of the reaction. The yield of CH4 first increased upon increasing the amount of Pt deposited on the g-C3N4 from 0 to 1 wt%, then decreased at 2 wt% Pt loading. The production rates of CH3OH and HCHO also increased with the content of Pt increasing from 0 to 0.75 wt% and the maximum yield was observed at 0.75 wt%. The Pt nanoparticles (NPs) could facilitate the transfer and enrichment of photogenerated electrons from g-C3N4 to its surface for photocatalytic reduction of CO2. At the same time, Pt was also used a catalyst to promote the oxidation of products. The transient photocurrent response further confirmed the proposed photocatalytic reduction mechanism of CO2. This work indicates that the deposition of Pt is a good strategy to improve the photoactivity and selectivity of g-C3N4 for CO2 reduction.

  11. Highly Efficient and Visible Light Responsive Heterojunction Composites as Dual Photoelectrodes for Photocatalytic Fuel Cell

    Directory of Open Access Journals (Sweden)

    Honghui Pan

    2018-01-01

    Full Text Available In the present work, a novel photocatalytic fuel cell (PFC system involving a dual heterojunction photoelectrodes, viz. polyaniline/TiO2 nanotubes (PANI/TiO2 NTs photoanode and CuO/Co3O4 nanorods (CuO/Co3O4 NRs photocathode, has been designed. Compared to TiO2 NTs electrode of PFC, the present heterojunction design not only enhances the visible light absorption but also offers the higher efficiency in degrading Rhodamine B–a model organic pollutant. The study includes an evaluation of the dual performance of the photoelectrodes as well. Under visible-light irradiation of 3 mW cm−2, the cell composed of the photoanode PANI/TiO2 NTs and CuO/Co3O4 NRs photocathode forms an interior bias of +0.24 V within the PFC system. This interior bias facilitated the transfer of electrons from the photoanode to photocathode across the external circuit and combined with the holes generated therein along with a simultaneous power production. In this manner, the separation of electron/hole pair was achieved in the photoelectrodes by releasing the holes and electrons of PANI/TiO2 NTs photoanode and CuO/Co3O4 NRs photocathode, respectively. Using this PFC system, the degradation of Rhodamine B in aqueous media was achieved to an extent of 68.5% within a reaction duration of a four-hour period besides a simultaneous power generation of 85 μA cm−2.

  12. Converting hazardous organics into clean energy using a solar responsive dual photoelectrode photocatalytic fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Li, Jianyong; Li, Jinhua, E-mail: lijinhua@sjtu.edu.cn; Chen, Quanpeng; Bai, Jing; Zhou, Baoxue

    2013-11-15

    Highlights: • A dual photoelcetrode PFC for converting hazardous organics into electricity. • The PFC possesses high cell performance operating in various model compounds. • Parameters were studied for optimization of the PFC performance. • Significant removal rate of chroma was observed in azo dyes solutions. -- Abstract: Direct discharging great quantities of organics into water-body not only causes serious environmental pollution but also wastes energy sources. In this paper, a solar responsive dual photoelectrode photocatalytic fuel cell (PFC{sup 2}) based on TiO{sub 2}/Ti photoanode and Cu{sub 2}O/Cu photocathode was designed for hazardous organics treatment with simultaneous electricity generation. Under solar irradiation, the interior bias voltage produced for the Fermi level difference between photoelectrodes drives photoelectrons of TiO{sub 2}/Ti photoanode to combine with photoholes of Cu{sub 2}O/Cu photocathode through external circuit thus generating electricity. In the meantime, organics are decomposed by photoholes remained at TiO{sub 2}/Ti photoanode. By using various hazardous organics including azo dyes as model pollutants, the PFC showed high converting performance of organics into electricity. For example, in 0.05 M phenol solution, a short-circuit current density 0.23 mA cm{sup −2}, open-circuit voltage 0.49 V, maximum power output 0.36 10{sup −4} W cm{sup −2} was achieved. On the other hand, removal rate of chroma reached 67%, 87% and 63% in 8 h for methyl orange, methylene blue, Congo red, respectively.

  13. Optimization of degradation of Reactive Black 5 (RB5) and electricity generation in solar photocatalytic fuel cell system.

    Science.gov (United States)

    Khalik, Wan Fadhilah; Ho, Li-Ngee; Ong, Soon-An; Voon, Chun-Hong; Wong, Yee-Shian; Yusoff, NikAthirah; Lee, Sin-Li; Yusuf, Sara Yasina

    2017-10-01

    The photocatalytic fuel cell (PFC) system was developed in order to study the effect of several operating parameters in degradation of Reactive Black 5 (RB5) and its electricity generation. Light irradiation, initial dye concentration, aeration, pH and cathode electrode are the operating parameters that might give contribution in the efficiency of PFC system. The degradation of RB5 depends on the presence of light irradiation and solar light gives better performance to degrade the azo dye. The azo dye with low initial concentration decolorizes faster compared to higher initial concentration and presence of aeration in PFC system would enhance its performance. Reactive Black 5 rapidly decreased at higher pH due to the higher amount of OH generated at higher pH and Pt-loaded carbon (Pt/C) was more suitable to be used as cathode in PFC system compared to Cu foil and Fe foil. The rapid decolorization of RB5 would increase their voltage output and in addition, it would also increase their V oc , J sc and P max . The breakage of azo bond and aromatic rings was confirmed through UV-Vis spectrum and COD analysis. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. New nanostructured silica incorporated with isolated Ti material for the photocatalytic conversion of CO2 to fuels

    Science.gov (United States)

    2014-01-01

    In this work, new nanoporous silica (Korea Advanced Institute of Science and Technology-6 (KIT-6)-dried or KIT-6-calcined) incorporated with isolated Ti materials with different Si/Ti ratios (Si/Ti = 200, 100, and 50) has been synthesized and investigated to establish photocatalytic reduction of CO2 in the presence of H2O vapors. The properties of the materials have been characterized through N2 adsorption/desorption, UV-vis, TEM, FT-IR, and XPS analysis techniques. The intermediate amount of the isolated Ti (Si/Ti = 100) has resulted to be more uniformly distributed on the surface and within the three-dimensional pore structure of the KIT-6 material, without its structure collapsing, than the other two ratios (Si/Ti = 200 and 50). However, titania agglomerates have been observed to have formed due to the increased Ti content (Si/Ti = 50). The Ti-KIT-6 (calcined) materials in the reaction showed higher activity than the Ti-KIT-6 (dried) materials, which produced CH4, H2, CO, and CH3OH (vapors) as fuel products. The Ti-KIT-6 (Si/Ti = 100) material also showed more OH groups, which are useful to obtain a higher production rate of the products, particularly methane, which was even higher than the rate of the best commercial TiO2 (Aeroxide P25, Evonik Industries AG, Essen, Germany) photocatalyst. PMID:24690396

  15. Solar Fuels: Photocatalytic Water Splitting Using a 2‐Photon Approach

    DEFF Research Database (Denmark)

    Seger, Brian; Mei, Bastian Timo; Bae, Dowon

    2014-01-01

    While the sun provides orders of magnitude more energy than we consume on earth, it is intermittent, and thus we must have storage reservoirs for when it is dark. Plants have realized early on that storing this energy in the form of molecular fuels is quite effective. In our work, we take...... a similarapproach and look to use solar cells to electrolyze water into hydrogen fuel and an oxygen byproduct. Modelling has shown that to optimize photoelectrolysis efficiency, a 2 photon tandem device (back toback solar cells) should be used. The underlying principle is that one solar cell should absorb high...... these issues and how to integrate them seamlessly together. In this talk I will discuss a) our optimizations of our solar cell, b) how we protect the solar cells from corrosion and c) our H2 and O2evolution catalysts. The talk will focus on what areas of the device we think are highly optimized and whatareas...

  16. Photocatalytic conversion of CO2 into value-added and renewable fuels

    Science.gov (United States)

    Yuan, Lan; Xu, Yi-Jun

    2015-07-01

    The increasing energy crisis and the worsening global climate caused by the excessive utilization of fossil fuel have boosted tremendous research activities about CO2 capture, storage and utilization. Artificial photosynthesis that uses solar light energy to convert CO2 to form value-added and renewable fuels such as methane or methanol has been consistently drawing increasing attention. It is like killing two birds with one stone since it can not only reduce the greenhouse effects caused by CO2 emission but also produce value added chemicals for alternative energy supplying. This review provides a brief introduction about the basic principles of artificial photosynthesis of CO2 and the progress made in exploring more efficient photocatalysts from the viewpoint of light harvesting and photogenerated charge carriers boosting. Moreover, the undergoing mechanisms of CO2 photoreduction are discussed with selected examples, in terms of adsorption of reactants, CO2 activation as well as the possible reaction pathways. Finally, perspectives on future research directions and open issues in CO2 photoreduction are outlined.

  17. Solar2Fuel: XPS and TPD characterization of functionalized TiO{sub 2} surfaces for photocatalytic reduction of CO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Staier, Florian; Grunze, Michael; Zharnikov, Michael [Angewandte Physikalische Chemie, Universitaet Heidelberg, INF 253, 69120 Heidelberg (Germany)

    2011-07-01

    The handling of CO{sub 2} produced by industrial installations and power plants has become a very important environmental issue nowadays because of it's generally accepted impact on the green house effect. In this context, a storage of CO{sub 2} or its conversation to fuel or useful chemicals are highly desirable. Along these lines, the solar2fuel project, funded by BMBF, aims on photocatalytic conversion of CO{sub 2} to methanol with a sufficient quantum efficiency which can justify and make rentable an industrial realization of the process. As the primary catalytic system TiO{sub 2} nanoparticle powder coatings are used. These particles are doped with metals to enhance their catalytic activity and functionalized with specially designed dyes which promote photocatalytic reaction and move the absorption spectrum from UV (characteristic of TiO{sub 2}) to the visible range. We present first results on characterization of these catalytic systems by several complimentary techniques as well as on temperature-programmed-desorption of CO{sub 2} and methanol from these functionalized surfaces.

  18. Status and perspectives of CO2 conversion into fuels and chemicals by catalytic, photocatalytic and electrocatalytic processes

    NARCIS (Netherlands)

    Kondratenko, E.V.; Mul, Guido; Baltrusaitis, Jonas; Larrazábal, G.O.; Pérez-Ramírez, J.

    2013-01-01

    This review highlights recent developments and future perspectives in carbon dioxide usage for the sustainable production of energy and chemicals and to reduce global warming. We discuss the heterogeneously catalysed hydrogenation, as well as the photocatalytic and electrocatalytic conversion of CO2

  19. Green-fuel-mediated synthesis of self-assembled NiO nano-sticks for dual applications—photocatalytic activity on Rose Bengal dye and antimicrobial action on bacterial strains

    Science.gov (United States)

    Iyyappa Rajan, P.; Vijaya, J. Judith; Jesudoss, S. K.; Kaviyarasu, K.; Kennedy, L. John; Jothiramalingam, R.; Al-Lohedan, Hamad A.; Vaali-Mohammed, Mansoor-Ali

    2017-08-01

    With aim of promoting the employability of green fuels in the synthesis of nano-scaled materials with new kinds of morphologies for multiple applications, successful synthesis of self-assembled NiO nano-sticks was achieved through a 100% green-fuel-mediated hot-plate combustion reaction. The synthesized NiO nano-sticks show excellent photocatalytic activity on Rose Bengal dye and superior antibacterial potential towards both Gram-positive and Gram-negative bacteria.

  20. Tapioca starch: An efficient fuel in gel-combustion synthesis of photocatalytically and anti-microbially active ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ramasami, Alamelu K. [Centre for Nano and Material Sciences, Jain University, Jakkasandra, Kanakapura (T) (India); Raja Naika, H. [Dept. of Biotechnology, University College of Science, Tumkur University, Tumkur (India); Nagabhushana, H. [CNR Rao Centre for Advanced Materials, Tumkur University, Tumkur (India); Ramakrishnappa, T.; Balakrishna, Geetha R. [Centre for Nano and Material Sciences, Jain University, Jakkasandra, Kanakapura (T) (India); Nagaraju, G., E-mail: nagarajugn@rediffmail.com [Centre for Nano and Material Sciences, Jain University, Jakkasandra, Kanakapura (T) (India); Dept. of Chemistry, Siddaganga Institute of Technology, Tumkur (India)

    2015-01-15

    Zinc oxide nanoparticles were synthesized by gel-combustion method using novel bio-fuel tapioca starch pearls, derived from the tubers of Manihotesculenta. The product is characterized using various techniques. The X-ray diffraction pattern correspond to a hexagonal zincite structure. Fourier transform infrared spectrum showed main absorption peaks at 394 and 508 cm{sup −} {sup 1} due to stretching vibration of Zn–O. Ultravoilet–visible spectrum of zinc oxide nanoparticles showed absorption maximum at 373 nm whereas the maximum of the bulk zinc oxide was 377 nm. The morphology of the product was studied using scanning electron microscopy and transmission electron microscopy. The scanning electron microscopic images showed that the products are agglomerated and porous in nature. The transmission electron microscopic images revealed spherical particles of 40–50 nm in diameter. The photocatalytic degradation of methylene blue was examined using zinc oxide nanoparticles and found more efficient in sunlight than ultra-violet light due to reduced band gap. The antibacterial properties of zinc oxide nanoparticles were investigated against four bacterial strains Klebsiella aerogenes, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aereus, where Pseudomonas aeruginosa and Staphylococcus aereus exhibited significant antibacterial activity in agar well diffusion method when compared to positive control. - Highlights: • ZnO nanoparticles have been prepared from a new bio-fuel, tapioca starch by gel combustion method. • XRD pattern revealed hexagonal zincite crystal structure with crystallite size 33 nm. • ZnO nanoparticles exhibited a band gap of 2.70 eV. • The ZnO nanoparticles exhibited superior degradation in sunlight in comparison with UV light. • The product showed a good anti-bacterial activity against two bacterial strains.

  1. SYNTHESIS, CHARACTERIZATION AND PHOTOCATALYTIC ...

    African Journals Online (AJOL)

    ISSN 1011-3924. © 2018 Chemical Society of Ethiopia and The Authors. Printed in Ethiopia ... SYNTHESIS, CHARACTERIZATION AND PHOTOCATALYTIC ACTIVITY OF .... cm−1 to determine the surface functional groups. 10 mg of sample ...

  2. Photocatalytic/Magnetic Composite Particles

    Science.gov (United States)

    Wu, Chang-Yu; Goswami, Yogi; Garretson, Charles; Andino, Jean; Mazyck, David

    2007-01-01

    Photocatalytic/magnetic composite particles have been invented as improved means of exploiting established methods of photocatalysis for removal of chemical and biological pollutants from air and water. The photocatalytic components of the composite particles are formulated for high levels of photocatalytic activity, while the magnetic components make it possible to control the movements of the particles through the application of magnetic fields. The combination of photocatalytic and magnetic properties can be exploited in designing improved air- and water treatment reactors.

  3. Applications of Photocatalytic Disinfection

    Directory of Open Access Journals (Sweden)

    Joanne Gamage

    2010-01-01

    Full Text Available Due to the superior ability of photocatalysis to inactivate a wide range of harmful microorganisms, it is being examined as a viable alternative to traditional disinfection methods such as chlorination, which can produce harmful byproducts. Photocatalysis is a versatile and effective process that can be adapted for use in many applications for disinfection in both air and water matrices. Additionally, photocatalytic surfaces are being developed and tested for use in the context of “self-disinfecting” materials. Studies on the photocatalytic technique for disinfection demonstrate this process to have potential for widespread applications in indoor air and environmental health, biological, and medical applications, laboratory and hospital applications, pharmaceutical and food industry, plant protection applications, wastewater and effluents treatment, and drinking water disinfection. Studies on photocatalytic disinfection using a variety of techniques and test organisms are reviewed, with an emphasis on the end-use application of developed technologies and methods.

  4. Assessing photocatalytic power of g-C3N4 for solar fuel production: A first-principles study involving quasi-particle theory and dispersive forces.

    Science.gov (United States)

    Osorio-Guillén, J M; Espinosa-García, W F; Moyses Araujo, C

    2015-09-07

    First-principles quasi-particle theory has been employed to assess catalytic power of graphitic carbon nitride, g-C3N4, for solar fuel production. A comparative study between g-h-triazine and g-h-heptazine has been carried out taking also into account van der Waals dispersive forces. The band edge potentials have been calculated using a recently developed approach where quasi-particle effects are taken into account through the GW approximation. First, it was found that the description of ground state properties such as cohesive and surface formation energies requires the proper treatment of dispersive interaction. Furthermore, through the analysis of calculated band-edge potentials, it is shown that g-h-triazine has high reductive power reaching the potential to reduce CO2 to formic acid, coplanar g-h-heptazine displays the highest thermodynamics force toward H2O/O2 oxidation reaction, and corrugated g-h-heptazine exhibits a good capacity for both reactions. This rigorous theoretical study shows a route to further improve the catalytic performance of g-C3N4.

  5. Photocatalytic degradation of H2S aqueous media using sulfide nanostructured solid-solution solar-energy-materials to produce hydrogen fuel.

    Science.gov (United States)

    Lashgari, Mohsen; Ghanimati, Majid

    2018-03-05

    H 2 S is a corrosive, flammable and noxious gas, which can be neutralized by dissolving in alkaline media and employed as H 2 -source by utilizing inside semiconductor-assisted/photochemical reactors. Herein, through a facile hydrothermal route, a ternary nanostructured solid-solution of iron, zinc and sulfur was synthesized in the absence and presence of Ag-dopant, and applied as efficient photocatalyst of hydrogen fuel production from H 2 S media. The effect of pH on the photocatalyst performance was scrutinized and the maximum activity was attained at pH=11, where HS - concentration is high. BET, diffuse reflectance and photoluminescence studies indicated that the ternary solid-solution photocatalyst, in comparison to its solid-solvent (ZnS), has a greater surface area, stronger photon absorption and less charge recombination, which justify its superiority. Moreover, the effect of silver-dopant on the photocatalyst performance was examined. The investigations revealed that although silver could boost the absorption of photons and increase the surface area, it could not appreciably enhance the photocatalyst performance due to its weak influence on retarding the charge-recombination process. Finally, the phenomenon was discussed in detail from mechanistic viewpoint. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Construction of an all-solid-state artificial Z-scheme system consisting of Bi2WO6/Au/CdS nanostructure for photocatalytic CO2 reduction into renewable hydrocarbon fuel

    Science.gov (United States)

    Wang, Meng; Han, Qiutong; Li, Liang; Tang, Lanqin; Li, Haijin; Zhou, Yong; Zou, Zhigang

    2017-07-01

    An all-solid-state Bi2WO6/Au/CdS Z-scheme system was constructed for the photocatalytic reduction of CO2 into methane in the presence of water vapor. This Z-scheme consists of ultrathin Bi2WO6 nanoplates and CdS nanoparticles as photocatalysts, and a Au nanoparticle as a solid electron mediator offering a high speed charge transfer channel and leading to more efficient spatial separation of electron-hole pairs. The photo-generated electrons from the conduction band (CB) of Bi2WO6 transfer to the Au, and then release to the valence band (VB) of CdS to recombine with the holes of CdS. It allows the electrons remaining in the CB of CdS and holes in the VB of Bi2WO6 to possess strong reduction and oxidation powers, respectively, leading the Bi2WO6/Au/CdS to exhibit high photocatalytic reduction of CO2, relative to bare Bi2WO6, Bi2WO6/Au, and Bi2WO6/CdS. The depressed hole density on CdS also enhances the stability of the CdS against photocorrosion.

  7. Surface modification and enhanced photocatalytic CO{sub 2} reduction performance of TiO{sub 2}: a review

    Energy Technology Data Exchange (ETDEWEB)

    Low, Jingxiang; Cheng, Bei [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Luoshi Road 122, Wuhan 430070 (China); Yu, Jiaguo, E-mail: jiaguoyu@yahoo.com [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Luoshi Road 122, Wuhan 430070 (China); Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah 21589 (Saudi Arabia)

    2017-01-15

    Highlights: • Application of modified TiO{sub 2} for photocatalytic CO{sub 2} reduction is summarized. • Different surface modification strategies of TiO{sub 2} are highlighted. • Summary and future perspectives in photocatalytic CO{sub 2} reduction are presented. - Abstract: Recently, the excessive consumption of fossil fuels has caused high emissions of the greenhouse gases, CO{sub 2} into atmosphere and global energy crisis. Mimicking the natural photosynthesis by using semiconductor materials to achieve photocatalytic CO{sub 2} reduction into valuable solar fuels such as CH{sub 4}, HCO{sub 2}H, CH{sub 2}O, and CH{sub 3}OH is known as one of the best solutions for addressing the aforementioned issue. Among various proposed photocatalysts, TiO{sub 2} has been extensively studied over the past several decades for photocatalytic CO{sub 2} reduction because of its cheapness and environmental friendliness. Particularly, surface modification of TiO{sub 2} has attracted numerous interests due to its capability of enhancing the light absorption ability, facilitating the electron-hole separation, tuning the CO{sub 2} reduction selectivity and increasing the CO{sub 2} adsorption and activation ability of TiO{sub 2} for photocatalytic CO{sub 2} reduction. In this review, recent approaches of the surface modification of TiO{sub 2} for photocatalytic CO{sub 2} reduction, including impurity doping, metal deposition, alkali modification, heterojunction construction and carbon-based material loading, are presented. The photocatalytic CO{sub 2} reduction mechanism and pathways of TiO{sub 2} are discussed. The future research direction and perspective of photocatalytic CO{sub 2} reduction over surface-modified TiO{sub 2} are also presented.

  8. Dye-Sensitized Photocatalytic Water Splitting and Sacrificial Hydrogen Generation: Current Status and Future Prospects

    Directory of Open Access Journals (Sweden)

    Pankaj Chowdhury

    2017-05-01

    Full Text Available Today, global warming and green energy are important topics of discussion for every intellectual gathering all over the world. The only sustainable solution to these problems is the use of solar energy and storing it as hydrogen fuel. Photocatalytic and photo-electrochemical water splitting and sacrificial hydrogen generation show a promise for future energy generation from renewable water and sunlight. This article mainly reviews the current research progress on photocatalytic and photo-electrochemical systems focusing on dye-sensitized overall water splitting and sacrificial hydrogen generation. An overview of significant parameters including dyes, sacrificial agents, modified photocatalysts and co-catalysts are provided. Also, the significance of statistical analysis as an effective tool for a systematic investigation of the effects of different factors and their interactions are explained. Finally, different photocatalytic reactor configurations that are currently in use for water splitting application in laboratory and large scale are discussed.

  9. Twin defects engineered Pd cocatalyst on C3N4 nanosheets for enhanced photocatalytic performance in CO2 reduction reaction

    Science.gov (United States)

    Lang, Qingqing; Hu, Wenli; Zhou, Penghui; Huang, Tianlong; Zhong, Shuxian; Yang, Lining; Chen, Jianrong; Bai, Song

    2017-12-01

    Photocatalytic conversion of CO2 to value-added chemicals, a potential route to addressing the depletion of fossil fuels and anthropogenic climate change, is greatly limited by the low-efficient semiconductor photocatalyst. The integration of cocatalyst with light-harvesting semiconductor is a promising approach to enhancing the photocatalytic performance in CO2 reduction reaction. The enhancement is greatly determined by the catalytic active sites on the surface of cocatalyst. Herein, we demonstrate that the photocatalytic performance in the CO2 reduction reaction is greatly promoted by twin defects engineered Pd cocatalyst. In this work, Pd nanoicosahedrons with twin defects were in situ grown on C3N4 nanosheets, which effectively improve the photocatalytic performance in reduction of CO2 to CO and CH4 in comparison with Pd nanotetrahedrons without twin defects. It is proposed that the twin boundary (TB) terminations on the surface of Pd cocatalysts are highly catalytic active sites for CO2 reduction reaction. Based on the proposed mechanism, the photocatalytic activity and selectivity in CO2 reduction were further advanced through reducing the size of Pd icosahedral cocatalyst resulted from the increased surface density of TB terminations. The defect engineering on the surface of cocatalyst represents a novel route in realizing high-performance photocatalytic applications.

  10. Photocatalytic Hybrid Semiconductor-Metal Nanoparticles; from Synergistic Properties to Emerging Applications.

    Science.gov (United States)

    Waiskopf, Nir; Ben-Shahar, Yuval; Banin, Uri

    2018-04-14

    Hybrid semiconductor-metal nanoparticles (HNPs) manifest unique combined and often synergetic properties stemming from the materials combination. These structures exhibit spatial charge separation across the semiconductor-metal junction upon light absorption, enabling their use as photocatalysts. So far, the main impetus of photocatalysis research in HNPs addresses their functionality in solar fuel generation. Recently, it was discovered that HNPs are functional in efficient photocatalytic generation of reactive oxygen species (ROS). This has opened the path for their implementation in diverse biomedical and industrial applications where high spatially temporally resolved ROS formation is essential. Here, the latest studies on the synergistic characteristics of HNPs are summarized, including their optical, electrical, and chemical properties and their photocatalytic function in the field of solar fuel generation is briefly discussed. Recent studies are then focused concerning photocatalytic ROS formation with HNPs under aerobic conditions. The emergent applications of this capacity are then highlighted, including light-induced modulation of enzymatic activity, photodynamic therapy, antifouling, wound healing, and as novel photoinitiators for 3D-printing. The superb photophysical and photocatalytic properties of HNPs offer already clear advantages for their utility in scenarios requiring on-demand light-induced radical formation and the full potential of HNPs in this context is yet to be revealed. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Enhanced photocatalytic CO₂-reduction activity of electrospun mesoporous TiO₂ nanofibers by solvothermal treatment.

    Science.gov (United States)

    Fu, Junwei; Cao, Shaowen; Yu, Jiaguo; Low, Jingxiang; Lei, Yongpeng

    2014-06-28

    Photocatalytic reduction of CO2 into renewable hydrocarbon fuels using semiconductor photocatalysts is considered as a potential solution to the energy deficiency and greenhouse effect. In this work, mesoporous TiO2 nanofibers with high specific surface areas and abundant surface hydroxyl groups are prepared using an electrospinning strategy combined with a subsequent calcination process, followed by a solvothermal treatment. The solvothermally treated mesoporous TiO2 nanofibers exhibit excellent photocatalytic performance on CO2 reduction into hydrocarbon fuels. The significantly improved photocatalytic activity can be attributed to the enhanced CO2 adsorption capacity and the improved charge separation after solvothermal treatment. The highest activity is achieved for the sample with a 2-h solvothermal treatment, showing 6- and 25-fold higher CH4 production rate than those of TiO2 nanofibers without solvothermal treatment and P25, respectively. This work may also provide a prototype for studying the effect of solvothermal treatment on the structure and photocatalytic activity of semiconductor photocatalysts.

  12. Photocatalytic water splitting: Quantitative approaches toward photocatalysis by design

    KAUST Repository

    Takanabe, Kazuhiro

    2017-10-11

    A widely used term, “photocatalysis”, generally addresses photocatalytic (energetically down-hill) and photosynthetic (energetically up-hill) reactions and refers to the use of photonic energy as a driving force for chemical transformations, i.e., electron reorganization to form/break chemical bonds. Although there are many such important reactions, this contribution focuses on the fundamental aspects of photocatalytic water splitting into hydrogen and oxygen by using light from the solar spectrum, which is one of the most investigated photosynthetic reactions. Photocatalytic water splitting using solar energy is considered to be artificial photosynthesis that produces a solar fuel because the reaction mimics nature’s photosynthesis not only in its redox reaction type but also in its thermodynamics (water splitting: 1.23 eV vs. glucose formation: 1.24 eV). To achieve efficient photocatalytic water splitting, all of the parameters, though involved at different timescales and spatial resolutions, should be optimized because the overall efficiency is obtained as the multiplication of all these fundamental efficiencies. The purpose of this review article is to provide the guidelines of a concept, “photocatalysis by design”, which is the opposite of “black box screening”; this concept refers to making quantitative descriptions of the associated physical and chemical properties to determine which events/parameters have the most impact on improving the overall photocatalytic performance, in contrast to arbitrarily ranking different photocatalyst materials. First, the properties that can be quantitatively measured or calculated are identified. Second, the quantities of these identified properties are determined by performing adequate measurements and/or calculations. Third, the obtained values of these properties are integrated into equations so that the kinetic/energetic bottlenecks of specific properties/processes can be determined, and the properties can

  13. Photocatalytic water splitting: Quantitative approaches toward photocatalysis by design

    KAUST Repository

    Takanabe, Kazuhiro

    2017-01-01

    A widely used term, “photocatalysis”, generally addresses photocatalytic (energetically down-hill) and photosynthetic (energetically up-hill) reactions and refers to the use of photonic energy as a driving force for chemical transformations, i.e., electron reorganization to form/break chemical bonds. Although there are many such important reactions, this contribution focuses on the fundamental aspects of photocatalytic water splitting into hydrogen and oxygen by using light from the solar spectrum, which is one of the most investigated photosynthetic reactions. Photocatalytic water splitting using solar energy is considered to be artificial photosynthesis that produces a solar fuel because the reaction mimics nature’s photosynthesis not only in its redox reaction type but also in its thermodynamics (water splitting: 1.23 eV vs. glucose formation: 1.24 eV). To achieve efficient photocatalytic water splitting, all of the parameters, though involved at different timescales and spatial resolutions, should be optimized because the overall efficiency is obtained as the multiplication of all these fundamental efficiencies. The purpose of this review article is to provide the guidelines of a concept, “photocatalysis by design”, which is the opposite of “black box screening”; this concept refers to making quantitative descriptions of the associated physical and chemical properties to determine which events/parameters have the most impact on improving the overall photocatalytic performance, in contrast to arbitrarily ranking different photocatalyst materials. First, the properties that can be quantitatively measured or calculated are identified. Second, the quantities of these identified properties are determined by performing adequate measurements and/or calculations. Third, the obtained values of these properties are integrated into equations so that the kinetic/energetic bottlenecks of specific properties/processes can be determined, and the properties can

  14. Nanocrystals and Nanoclusters as Cocatalysts for Photocatalytic Water Splitting

    KAUST Repository

    Sinatra, Lutfan

    2016-12-04

    The energy consumptions worldwide have increased simultaneously with the growth of the population and of the economy. Nowadays, finding an alternative way to satisfy the energy demand is one of the great challenges for the future of humanity, especially due to the limitation of fossil fuels and their effect on global warming. Hydrogen, as an alternative fuel for the future, is very attractive. Compared to traditional methods, such as the steam reforming of natural gas or coal gasification, photocatalytic water splitting (PWS) is considered to be the most sustainable alternative for producing hydrogen as a future fuel. PWS usually relies on semiconductor material that can transform the absorbed solar photon into photogenerated electrons and holes, creating a photopotential which can drive the electrochemical production of molecular hydrogen from the reduction of water. Despite its promising application, semiconductor-based PWS usually suffers from low carrier mobility and short diffusion length. Furthermore, the recombination of photogenerated electrons and holes might occur, especially if there are no suitable reaction sites available on the surface of the semiconductor. In order to facilitate the catalytic reactions on the surface of the semiconductor, the presence of a cocatalyst is necessary in order to obtain more efficient PWS processes. To this day, noble metals such as Pt, Pd, RuO2 and IrO2 are still the benchmark cocatalysts for PWS. Nevertheless, due to their high cost and limited supply, it is mandatory to develop a suitable strategy and to identify more efficient materials. Therefore, within the framework of this dissertation, novel cocatalysts and strategies that can improve the efficiency of the photocatalytic water splitting processes have been developed. Firstly, we developed a cocatalyst combining noble metals and semiconductors by means of partial galvanic replacement of the Cu2O nanocrystal with Au. The deposition of this cocatalyst on TiO2 was

  15. Photocatalytic conversion of methane to methanol

    Energy Technology Data Exchange (ETDEWEB)

    Taylor, C.E.; Noceti, R.P.; D`Este, J.R. [Pittsburgh Energy Technology Center, PA (United States)

    1995-12-31

    A long-term goal of our research group is the exploration of novel pathways for the direct oxidation of methane to liquid fuels, chemicals, and intermediates. The use of three relatively abundant and inexpensive reactants, light, water, and methane, to produce methanol is attractive. The products of reaction, methanol and hydrogen, are both commercially desirable, methanol being used as is or converted to a variety of other chemicals, and the hydrogen could be utilized in petroleum and/or chemical manufacturing. Methane is produced as a by-product of coal gasification. Depending upon reactor design and operating conditions, up to 18% of total gasifier product may be methane. In addition, there are vast proven reserves of geologic methane in the world. Unfortunately, a large fraction of these reserves are in regions where there is little local demand for methane and it is not economically feasible to transport it to a market. There is a global research effort under way in academia, industry, and government to find methods to convert methane to useful, more readily transportable and storable materials. Methanol, the initial product of methane oxidation, is a desirable product of conversion because it retains much of the original energy of the methane while satisfying transportation and storage requirements. Investigation of direct conversion of methane to transportation fuels has been an ongoing effort at PETC for over 10 years. One of the current areas of research is the conversion of methane to methanol, under mild conditions, using light, water, and a semiconductor photocatalyst. The use of three relatively abundant and inexpensive reactants, light, water, and methane, to produce methanol, is attractive. Research in the laboratory is directed toward applying the techniques developed for the photocatalytic splitting of the water and the photochemical conversion of methane.

  16. Porphyrin-based Photocatalytic Nanolithography

    Energy Technology Data Exchange (ETDEWEB)

    Bearinger, J P; Stone, G; Dugan, L C; Dasher, B E; Stockton, C; Conway, J W; Kuenzler, T; Hubbell, J A

    2009-06-08

    Nanoarray fabrication is a multidisciplinary endeavor encompassing materials science, chemical engineering and biology. We form nanoarrays via a new technique, porphyrin-based photocatalytic nanolithography (PCNL). The nanoarrays, with controlled features as small as 200 nm, exhibit regularly ordered patterns and may be appropriate for (a) rapid and parallel proteomic screening of immobilized biomolecules, (b) protein-protein interactions and/or (c) biophysical and molecular biology studies involving spatially dictated ligand placement. We demonstrate protein immobilization utilizing nanoarrays fabricated via PCNL on silicon substrates, where the immobilized proteins are surrounded by a non-fouling polymer background.

  17. Quantification of photocatalytic oxygenation of human blood.

    Science.gov (United States)

    Subrahmanyam, Aryasomayajula; Thangaraj, Paul R; Kanuru, Chandrasekhar; Jayakumar, Albert; Gopal, Jayashree

    2014-04-01

    Photocatalytic oxygenation of human blood is an emerging concept based on the principle of photocatalytic splitting of water into oxygen and hydrogen. This communication reports: (i) a design of a photocatalytic cell (PC) that separates the blood from UV (incident) radiation source, (ii) a pH, temperature and flow controlled circuit designed for quantifying the oxygenation of human blood by photocatalysis and (iii) measuring the current efficacy of ITO/TiO2 nano thin films in oxygenating human blood in a dynamic circuit in real time. The average increase in oxygen saturation was around 5% above baseline compared to control (p<0.0005). We believe this is one of the first attempts to quantify photocatalytic oxygenation of human blood under controlled conditions. Copyright © 2013 IPEM. Published by Elsevier Ltd. All rights reserved.

  18. Modeling intrinsic kinetics in immobilized photocatalytic microreactors

    NARCIS (Netherlands)

    Visan, Aura; Rafieian Boroujeni, Damon; Ogieglo, Wojciech; Lammertink, Rob G.H.

    2014-01-01

    The article presents a simple model for immobilized photocatalytic microreactors following a first order reaction rate with either light independency or light dependency described by photon absorption carrier generation semiconductor physics. Experimental data obtained for various residence times,

  19. Synthesis, characterization, photocatalytic and reusability studies of ...

    Indian Academy of Sciences (India)

    Administrator

    Although these dyes are an important part of textile industry but their discharge ... Till now, many conventional methods (chemical, physical, biological) have been ... these NPs show good photocatalytic activity due to trapped holes arising from ...

  20. Photocatalytic fluoroalkylation reactions of organic compounds

    OpenAIRE

    Barata Vallejo, Sebastian; Bonesi, Sergio Mauricio; Postigo, Jose Alberto

    2017-01-01

    Photocatalytic methods for fluoroalkyl-radical generation provide more convenient alternatives to the classical perfluoroalkyl-radical (Rf) production through chemical initiators, such as azo or peroxide compounds or the employment of transition metals through a thermal electron transfer (ET) initiation process. The mild photocatalytic reaction conditions tolerate a variety of functional groups and, thus, are handy to the late-stage modification of bioactive molecules. Transition metal-photoc...

  1. Advanced oxidation technologies : photocatalytic treatment of wastewater

    OpenAIRE

    Chen, J.

    1997-01-01

    7.1. Summary and conclusions

    The last two decennia have shown a growing interest in the photocatalytic treatment of wastewater, and more and more research has been carried out into the various aspects of photocatalysis, varying from highly fundamental aspects to practical application. However, despite all this research, there is still much to investigate. Suggested photocatalytic mechanisms, such as those for oxidation by hydroxyl radicals and for oxidation at the surface of photocata...

  2. Theoretical Investigation of Bismuth-Based Semiconductors for Photocatalytic Applications

    KAUST Repository

    Laradhi, Shaikhah

    2017-11-01

    Converting solar energy to clean fuel has gained remarkable attention as an emerged renewable energy resource but optimum efficiency in photocatalytic applications has not yet been reached. One of the dominant factors is designing efficient photocatalytic semiconductors. The research reveals a theoretical investigation of optoelectronic properties of bismuth-based metal oxide and oxysulfide semiconductors using highly accurate first-principles quantum method based on density functional theory along with the range-separated hybrid HSE06 exchange-correlation functional. First, bismuth titanate compounds including Bi12TiO20, Bi4Ti3O12, and Bi2Ti2O7 were studied in a combined experimental and theoretical approach to prove its photocatalytic activity under UV light. They have unique bismuth layered structure, tunable electronic properties, high dielectric constant and low electron and effective masses in one crystallographic direction allowing for good charge separation and carrier diffusion properties. The accuracy of the investigation was determined by the good agreement between experimental and theoretical values. Next, BiVO4 with the highest efficiency for oxygen evolution was investigated. A discrepancy between the experimental and theoretical bandgap was reported and inspired a systematic study of all intrinsic defects of the material and the corresponding effect on the optical and transport properties. A candidate defective structure was proposed for an efficient photocatalytic performance. To overcome the carrier transport limitation, a mild hydrogen treatment was also introduced. Carrier lifetime was enhanced due to a significant reduction of trap-assisted recombination, either via passivation of deep trap states or reduction of trap state density. Finally, an accurate theoretical approach to design a new family of semiconductors with enhanced optoelectronic properties for water splitting was proposed. We simulated the solid solutions Bi1−xRExCuOS (RE = Y, La

  3. for SERS and Photocatalytic Applications

    Directory of Open Access Journals (Sweden)

    Xue Chen

    2011-01-01

    Full Text Available ZnS/Si nanocables were synthesized via a simple two-step thermal evaporation method. The shape and diameter of the ZnS/Si nanocables can be controlled by adjusting the morphologies of the ZnS nanostructures (nanowire or nanoribbon obtained in the first step and the deposition time of the Si shell in the second step, respectively. Furthermore, we obtained polycrystalline Si nanotubes with different shapes and diameters by etching away the inner ZnS core. The as-prepared Si nanotubes were employed as SERS-active substrates, which exhibited a high sensitivity for the detection of R6G. The Si nanotubes also showed effective photocatalytic activity on the decomposition of R6G under the irradiation of visible light.

  4. Direct Coupling of Thermo- and Photocatalysis for Conversion of CO2 -H2 O into Fuels.

    Science.gov (United States)

    Zhang, Li; Kong, Guoguo; Meng, Yaping; Tian, Jinshu; Zhang, Lijie; Wan, Shaolong; Lin, Jingdong; Wang, Yong

    2017-12-08

    Photocatalytic CO 2 reduction into renewable hydrocarbon solar fuels is considered as a promising strategy to simultaneously address global energy and environmental issues. This study focused on the direct coupling of photocatalytic water splitting and thermocatalytic hydrogenation of CO 2 in the conversion of CO 2 -H 2 O into fuels. Specifically, it was found that direct coupling of thermo- and photocatalysis over Au-Ru/TiO 2 leads to activity 15 times higher (T=358 K; ca. 99 % CH 4 selectivity) in the conversion of CO 2 -H 2 O into fuels than that of photocatalytic water splitting. This is ascribed to the promoting effect of thermocatalytic hydrogenation of CO 2 by hydrogen atoms generated in situ by photocatalytic water splitting. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Cocatalysts in Semiconductor-based Photocatalytic CO2 Reduction: Achievements, Challenges, and Opportunities.

    Science.gov (United States)

    Ran, Jingrun; Jaroniec, Mietek; Qiao, Shi-Zhang

    2018-02-01

    Ever-increasing fossil-fuel combustion along with massive CO 2 emissions has aroused a global energy crisis and climate change. Photocatalytic CO 2 reduction represents a promising strategy for clean, cost-effective, and environmentally friendly conversion of CO 2 into hydrocarbon fuels by utilizing solar energy. This strategy combines the reductive half-reaction of CO 2 conversion with an oxidative half reaction, e.g., H 2 O oxidation, to create a carbon-neutral cycle, presenting a viable solution to global energy and environmental problems. There are three pivotal processes in photocatalytic CO 2 conversion: (i) solar-light absorption, (ii) charge separation/migration, and (iii) catalytic CO 2 reduction and H 2 O oxidation. While significant progress is made in optimizing the first two processes, much less research is conducted toward enhancing the efficiency of the third step, which requires the presence of cocatalysts. In general, cocatalysts play four important roles: (i) boosting charge separation/transfer, (ii) improving the activity and selectivity of CO 2 reduction, (iii) enhancing the stability of photocatalysts, and (iv) suppressing side or back reactions. Herein, for the first time, all the developed CO 2 -reduction cocatalysts for semiconductor-based photocatalytic CO 2 conversion are summarized, and their functions and mechanisms are discussed. Finally, perspectives in this emerging area are provided. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Electrochemical Sensing, Photocatalytic and Biological Activities of ZnO Nanoparticles: Synthesis via Green Chemistry Route

    Science.gov (United States)

    Yadav, L. S. Reddy; Archana, B.; Lingaraju, K.; Kavitha, C.; Suresh, D.; Nagabhushana, H.; Nagaraju, G.

    2016-05-01

    In this paper, we have successfully synthesized ZnO nanoparticles (Nps) via solution combustion method using sugarcane juice as the novel fuel. The structure and morphology of the synthesized ZnO Nps have been analyzed using various analytical tools. The synthesized ZnO Nps exhibit excellent photocatalytic activity for the degradation of methylene blue dye, indicating that the ZnO Nps are potential photocatalytic semiconductor materials. The synthesized ZnO Nps also show good electrochemical sensing of dopamine. ZnO Nps exhibit significant bactericidal activity against Klebsiella aerogenes, Pseudomonas aeruginosa, Eschesichia coli and Staphylococcus aureus using agar well diffusion method. Furthermore, the ZnO Nps show good antioxidant activity by potentially scavenging 1-diphenyl-2-picrylhydrazyl (DPPH) radicals. The above studies clearly demonstrate versatile applications of ZnO synthesized by simple eco-friendly route.

  7. Photocatalytic materials and technologies for air purification.

    Science.gov (United States)

    Ren, Hangjuan; Koshy, Pramod; Chen, Wen-Fan; Qi, Shaohua; Sorrell, Charles Christopher

    2017-03-05

    Since there is increasing concern for the impact of air quality on human health, the present work surveys the materials and technologies for air purification using photocatalytic materials. The coverage includes (1) current photocatalytic materials for the decomposition of chemical contaminants and disinfection of pathogens present in air and (2) photocatalytic air purification systems that are used currently and under development. The present work focuses on five main themes. First, the mechanisms of photodegradation and photodisinfection are explained. Second, system designs for photocatalytic air purification are surveyed. Third, the photocatalytic materials used for air purification and their characteristics are considered, including both conventional and more recently developed photocatalysts. Fourth, the methods used to fabricate these materials are discussed. Fifth, the most significant coverage is devoted to materials design strategies aimed at improving the performance of photocatalysts for air purification. The review concludes with a brief consideration of promising future directions for materials research in photocatalysis. Copyright © 2016 Elsevier B.V. All rights reserved.

  8. Photocatalytic paper using zinc oxide nanorods

    International Nuclear Information System (INIS)

    Baruah, Sunandan; Jaisai, Mayuree; Imani, Reza; Nazhad, Mousa M; Dutta, Joydeep

    2010-01-01

    Zinc oxide (ZnO) nanorods were grown on a paper support prepared from soft wood pulp. The photocatalytic activity of a sheet of paper with ZnO nanorods embedded in its porous matrix has been studied. ZnO nanorods were firmly attached to cellulose fibers and the photocatalytic paper samples were reused several times with nominal decrease in efficiency. Photodegradation of up to 93% was observed for methylene blue in the presence of paper filled with ZnO nanorods upon irradiation with visible light at 963 Wm -2 for 120 min. Under similar conditions, photodegradation of approximately 35% was observed for methyl orange. Antibacterial tests revealed that the photocatalytic paper inhibits the growth of Escherichia coli under room lighting conditions.

  9. Photocatalytic semiconductors synthesis, characterization, and environmental applications

    CERN Document Server

    Hernández-Ramírez, Aracely

    2014-01-01

    This critical volume examines the different methods used for the synthesis of a great number of photocatalysts, including TiO2, ZnO and other modified semiconductors, as well as characterization techniques used for determining the optical, structural and morphological properties of the semiconducting materials. Additionally, the authors discuss photoelectrochemical methods for determining the light activity of the photocatalytic semiconductors by means of measurement of properties such as band gap energy, flat band potential and kinetics of hole and electron transfer. Photocatalytic Semiconductors: Synthesis, Characterization and Environmental Applications provide an overview of the semiconductor materials from first- to third-generation photocatalysts and their applications in wastewater treatment and water disinfection. The book further presents economic and toxicological aspects in the production and application of photocatalytic materials.

  10. Correlation of Photocatalytic Activity with Band Structure of Low-dimensional Semiconductor Nanostructures

    Science.gov (United States)

    Meng, Fanke

    Photocatalytic hydrogen generation by water splitting is a promising technique to produce clean and renewable solar fuel. The development of effective semiconductor photocatalysts to obtain efficient photocatalytic activity is the key objective. However, two critical reasons prevent wide applications of semiconductor photocatalysts: low light usage efficiency and high rates of charge recombination. In this dissertation, several low-dimensional semiconductors were synthesized with hydrothermal, hydrolysis, and chemical impregnation methods. The band structures of the low-dimensional semiconductor materials were engineered to overcome the above mentioned two shortcomings. In addition, the correlation between the photocatalytic activity of the low-dimensional semiconductor materials and their band structures were studied. First, we studied the effect of oxygen vacancies on the photocatalytic activity of one-dimensional anatase TiO2 nanobelts. Given that the oxygen vacancy plays a significant role in band structure and photocatalytic performance of semiconductors, oxygen vacancies were introduced into the anatase TiO2 nanobelts during reduction in H2 at high temperature. The oxygen vacancies of the TiO2 nanobelts boosted visible-light-responsive photocatalytic activity but weakened ultraviolet-light-responsive photocatalytic activity. As oxygen vacancies are commonly introduced by dopants, these results give insight into why doping is not always beneficial to the overall photocatalytic performance despite increases in absorption. Second, we improved the photocatalytic performance of two-dimensional lanthanum titanate (La2Ti2 O7) nanosheets, which are widely studied as an efficient photocatalyst due to the unique layered crystal structure. Nitrogen was doped into the La2Ti2O7 nanosheets and then Pt nanoparticles were loaded onto the La2Ti2O7 nanosheets. Doping nitrogen narrowed the band gap of the La2Ti 2O7 nanosheets by introducing a continuum of states by the valence

  11. Photocatalytic reforming of biomass for hydrogen production

    NARCIS (Netherlands)

    Ripken, R.M.; de Boer, V.J.H.W.; Gardeniers, J.G.E.; le Gac, S.

    2017-01-01

    Here, we describe a novel microfluidic device to determine the required bandgap for the photocatalytic reforming of biomass model substrates (ethylene glycol, glycerol, xylose and xylitol) in water. Furthermore, this device is applied to eventually elucidate the reaction mechanism of aqueous

  12. Advanced oxidation technologies : photocatalytic treatment of wastewater

    NARCIS (Netherlands)

    Chen, J.

    1997-01-01

    7.1. Summary and conclusions

    The last two decennia have shown a growing interest in the photocatalytic treatment of wastewater, and more and more research has been carried out into the various aspects of photocatalysis, varying from highly fundamental aspects to practical application.

  13. Photocatalytic Solutions Create Self-Cleaning Surfaces

    Science.gov (United States)

    2013-01-01

    A Stennis Space Center researcher investigating the effectiveness of photocatalytic materials for keeping the Center's buildings free of grime turned to a solution created by PURETi Inc. of New York City. Testing proved successful, and NASA and the company now share a Dual Use Technology partnership. PURETi's coatings keep surfaces clean and purify surrounding air, eliminating pollution, odors, and microbes.

  14. Photoluminescence quenching and photocatalytic enhancement of ...

    Indian Academy of Sciences (India)

    2017-11-28

    Nov 28, 2017 ... This work reports the synthesis of novel praseodymium (Pr)-doped ZnO nanocrystals with excellent ... nificant role in the field of solar cells, luminescence, electrical, ..... 5.1 Photocatalytic activity mechanism in Pr-doped ZnO.

  15. Design and analysis of novel photocatalytic materials

    Science.gov (United States)

    Boppana, Venkata Bharat Ram

    The development of sustainable sources of energy to decrease our dependence on non-renewable fossil fuels and the reduction of emissions causing global warming are important technological challenges of the 21st century. Production of solar fuels by photocatalysis is one potential route to reduce the impact of those problems. The most widely applied photocatalyst is TiO2 because it is stable, non-toxic and inexpensive. Still, it cannot utilize the solar spectrum efficiently as its band gap is 3.2 eV thus able to absorb only 3% of sun light. This thesis therefore explores multiple avenues towards improving the light absorption capability of semiconductor materials without loss in activity. To achieve this objective, the valence band hybridization method of band gap reduction was utilized. This technique is based on introducing new orbitals at the top of valence band of the semiconductor that can then hybridize with existing orbitals. The hybridization then raises the maximum of the valence band thereby reducing the band gap. This technique has the added advantage of increasing the mobility of oxidizing holes in the now dispersed valence band. In practice, this can be achieved by introducing N 2p or Sn 5s orbitals in the valence band of an oxide. We initially designed novel zinc gallium oxy-nitrides, with the spinel structure and band gaps in the visible region of the solar spectrum, by nitridation of a zinc gallate precursor produced by sol-gel synthesis. These spinel oxy-nitrides have band gaps of 2.5 to 2.7 eV, surface areas of 16 to 36 m 2/g, and nitrogen content less than 1.5%. They are active towards degradation of organic molecules in visible light. Density functional theory calculations show that this band gap reduction in part is associated with hybridization between the dopant N 2p states with Zn 3d orbitals at the top of the valence band. While spinel oxy-nitrides are produced under nitridation at 550°C, at higher temperatures they are consumed to form

  16. Enhanced selective photocatalytic CO{sub 2} reduction into CO over Ag/CdS nanocomposites under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Zezhou; Qin, Jiani; Jiang, Min; Ding, Zhengxin; Hou, Yidong, E-mail: ydhou@fzu.edu.cn

    2017-01-01

    Highlights: • Ag/CdS nanocomposites were prepared by a facile photodeposition method. • Ag/CdS was more effective as a photocatalyst for CO{sub 2} reduction than CdS. • Ag as cocatalyst served as electron trap as well as active site for CO{sub 2} reduction reaction. - Abstract: Photocatalytic reduction of carbon dioxide can convert chemically inert carbon dioxide into useful chemical fuel in a mild manner. Herein, Ag-CdS nanocomposites were prepared by photodeposition method and examined for photocatalytic CO{sub 2} reduction under visible light. Meanwhile, the nanocomposites were characterized by XRD, SEM, TEM, XPS, DRS and PL in detail. The results show that, the deposition of Ag improves the photocatalytic performance of CdS, especially in the selectivity of CO{sub 2}-to-CO. The highest photocatalytic activity is achieved over 1.0 wt.% Ag/CdS, with an increase by 3 times in comparison to CdS. In this reaction system, Ag can serve as electron trap as well as active site for CO{sub 2} reduction, which is probably responsible for the enhanced activity and selectivity of CO{sub 2} to CO over Ag/CdS. The possible mechanism of CO{sub 2} photoreduction over Ag/CdS was proposed in view of the abovementioned analysis.

  17. Metal Nanoshells for Plasmonically Enhanced Solar to Fuel Photocatalytic Conversion

    Science.gov (United States)

    2016-05-18

    transfer, we anticipate this interlayer will modulate charge transfer from the metal to the semiconductor and vice versa. These new core-shell particles ...enhancement mechanism. In an extensive study using ten different samples, we found that GS-NS@ZIS particles with an LSPR absorption at ~700 nm and a silica...then coated with a thin layer of silica (SiO2), followed by a zinc indium sulfide (ZnIn2S4; ZIS) semiconductor shell. The blended-metal GS-NS cores

  18. Correlation of lattice distortion with photocatalytic activity of titanium dioxide

    International Nuclear Information System (INIS)

    Wang Xia; Shui Miao; Li Rongsheng; Song Yue

    2008-01-01

    The photocatalytic activity of titanium dioxide dispersions on X-3B pigment degradation has been investigated. A variety of factors that would influence the photocatalytic activity such as crystallite size, lattice distortion, and anatase content are discussed in detail. It is found that lattice distortion is the most important one among these factors and is expected to inhibit the hole and electron pair recombination. It determines, to some extent, the photocatalytic efficiency of titanium dioxide dispersions

  19. Understanding metal-organic frameworks for solar fuel production

    NARCIS (Netherlands)

    Garcia Santaclara, J.

    2017-01-01

    The fascinating chemical and physical properties of MOFs have recently stimulated exploration of their application for photocatalysis. Despite the intense research effort, the efficiencies of most photocatalytic MOFs for solar fuel generation are still very modest. In this introduction we analyse

  20. Enhanced photocatalytic H{sub 2} production on CdS nanorod using cobalt-phosphate as oxidation cocatalyst

    Energy Technology Data Exchange (ETDEWEB)

    Di, Tingmin; Zhu, Bicheng; Zhang, Jun; Cheng, Bei [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Yu, Jiaguo, E-mail: jiaguoyu@yahoo.com [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Faculty of Science, King Abdulaziz University, Jeddah 21589 (Saudi Arabia)

    2016-12-15

    Highlights: • Co-Pi/CdS composites were synthesized by a simple photodeposition method. • The composites showed superior photocatalytic H{sub 2} production activity. • The optimal H{sub 2} production rate of Co-Pi/CdS was even higher than that of Pt-CdS. • Co-Pi is a good oxidation cocatalyst used for capture of photogenerated hole. - Abstract: Employing visible light responsive semiconductor for photocatalytic hydrogen production by water splitting is an efficient way for utilizing renewable solar energy to solve the depletion of fossil fuel and environmental contamination. Herein, we report enhanced photocatalytic H{sub 2}-production performance over CdS nanorod using cobalt-phosphate (Co-Pi) as a water oxdation cocatalyst. The optimal Co-Pi modified CdS nanocomposite photocatalyst with the Co-Pi content of 8.4 mol% has a superior visible light H{sub 2}-production rate of 13.3 mmol h{sup −1} g{sup −1} with an apparent quantum efficiency of 24.3% at 420 nm, which is even higher than that of 1 wt% Pt-CdS (11.3 mmol h{sup −1} g{sup −1}) under the same conditions. The enhanced visible-light photocatalytic H{sub 2} production activity was attributed to the hole trapping and collecting ability of Co-Pi cocatalyst, which could effectively suppress the recombination of photogenerated electron-hole pairs and increase the electron density for hydrogen production. This work shows a possibility of using earth-abundant Co-Pi as cocatalyst for enhancing photocatalytic H{sub 2} production.

  1. Fuel Production from Seawater and Fuel Cells Using Seawater.

    Science.gov (United States)

    Fukuzumi, Shunichi; Lee, Yong-Min; Nam, Wonwoo

    2017-11-23

    Seawater is the most abundant resource on our planet and fuel production from seawater has the notable advantage that it would not compete with growing demands for pure water. This Review focuses on the production of fuels from seawater and their direct use in fuel cells. Electrolysis of seawater under appropriate conditions affords hydrogen and dioxygen with 100 % faradaic efficiency without oxidation of chloride. Photoelectrocatalytic production of hydrogen from seawater provides a promising way to produce hydrogen with low cost and high efficiency. Microbial solar cells (MSCs) that use biofilms produced in seawater can generate electricity from sunlight without additional fuel because the products of photosynthesis can be utilized as electrode reactants, whereas the electrode products can be utilized as photosynthetic reactants. Another important source for hydrogen is hydrogen sulfide, which is abundantly found in Black Sea deep water. Hydrogen produced by electrolysis of Black Sea deep water can also be used in hydrogen fuel cells. Production of a fuel and its direct use in a fuel cell has been made possible for the first time by a combination of photocatalytic production of hydrogen peroxide from seawater and dioxygen in the air and its direct use in one-compartment hydrogen peroxide fuel cells to obtain electric power. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Photocatalytic Water-Splitting Reaction from Catalytic and Kinetic Perspectives

    KAUST Repository

    Hisatomi, Takashi

    2014-10-16

    Abstract: Some particulate semiconductors loaded with nanoparticulate catalysts exhibit photocatalytic activity for the water-splitting reaction. The photocatalysis is distinct from the thermal catalysis because photocatalysis involves photophysical processes in particulate semiconductors. This review article presents a brief introduction to photocatalysis, followed by kinetic aspects of the photocatalytic water-splitting reaction.Graphical Abstract: [Figure not available: see fulltext.

  3. Photocatalytic decomposition of cortisone acetate in aqueous solution

    NARCIS (Netherlands)

    Sobral Romao, J.I.; Saad, M.H.; Mul, Guido; Baltrusaitis, Jonas

    2015-01-01

    The photocatalytic decomposition of cortisone 21-acetate (CA), a model compound for the commonly used steroid, cortisone, was studied. CA was photocatalytically decomposed in a slurry reactor with the initial rates between 0.11 and 0.46 mg L−1 min−1 at 10 mg L−1 concentration, using the following

  4. Alternative photocatalysts to TiO2 for the photocatalytic reduction of CO2

    Science.gov (United States)

    Nikokavoura, Aspasia; Trapalis, Christos

    2017-01-01

    The increased concentration of CO2 in the atmosphere, originating from the burning of fossil fuels in stationary and mobile sources, is referred as the "Anthropogenic Greenhouse Effect" and constitutes a major environmental concern. The scientific community is highly concerned about the resulting enhancement of the mean atmospheric temperature, so a vast diversity of methods has been applied. Thermochemical, electrochemical, photocatalytic, photoelectrochemical processes, as well as combination of solar electricity generation and water splitting processes have been performed in order to lower the CO2 atmospheric levels. Photocatalytic methods are environmental friendly and succeed in reducing the atmospheric CO2 concentration and producing fuels or/and useful organic compounds at the same time. The most common photocatalysts for the CO2 reduction are the inorganic, the carbon based semiconductors and the hybrids based on semiconductors, which combine stability, low cost and appropriate structure in order to accomplish redox reactions. In this review, inorganic semiconductors such as single-metal oxide, mixed-metal oxides, metal oxide composites, layered double hydroxides (LDHs), salt composites, carbon based semiconductors such as graphene based composites, CNT composites, g-C3N4 composites and hybrid organic-inorganic materials (ZIFs) were studied. TiO2 and Ti based photocatalysts are extensively studied and therefore in this review they are not mentioned.

  5. Photocatalytic Activity of Nanostructured Titanium Dioxide Thin Films

    Directory of Open Access Journals (Sweden)

    Zdenek Michalcik

    2012-01-01

    Full Text Available The aim of this paper is to investigate the properties and photocatalytic activity of nanostructured TiO2 layers. The glancing angle deposition method with DC sputtering at low temperature was applied for deposition of the layers with various columnar structures. The thin-film structure and surface morphology were analyzed by XRD, SEM, and AFM analyses. The photocatalytic activity of the films was determined by the rate constant of the decomposition of the Acid Orange 7. In dependence on the glancing angle deposition parameters, three types of columnar structures were obtained. The films feature anatase/rutile and/or amorphous structures depending on the film architecture and deposition method. All the films give the evidence of the photocatalytic activity, even those without proved anatase or rutile structure presence. The impact of columnar boundary in perspective of the photocatalytic activity of nanostructured TiO2 layers was discussed as the possible factor supporting the photocatalytic activity.

  6. Recovery of noble metals from HLLW using photocatalytic reduction

    International Nuclear Information System (INIS)

    Nishi, T.; Uetake, N.; Kawamura, F.; Yusa, H.

    1987-01-01

    In high-level liquid waste (HLLW) from fuel reprocessing plants, noble metals (palladium, rhodium, and ruthenium), which account for ∼ 10 wt% of fission products, exist as ions. These metals are very useful as catalytic material in automobile exhaust systems and other chemical processes, but they are rare in nature, making their recovery from fission products highly desirable. The ions of noble metals in solution have the feature that their reduction potential from ion to metal is relatively high compared with that of other fission product ions, so they can be selectively separated as a metal by a reduction process. The authors think a photoreduction process using a photocatalysts, which functions as photon-electron conversion agent, is suitable for the recovery of noble metals from HLLW for three reasons: (1) this process uses no reduction agents, which usually degrade the nitric acid, so that coprecipitation of other fission products does not occur. (2) The reactions are induced by light, which does not contaminate the reaction system, and in contrast with ordinary photo-redox reactions, the quantum yield is quite high. (3) As the photocatalyst does not change in the reaction, it can be used again and again. The report shows the results of fundamental experiments on the application of photocatalytic reduction to the recovery of noble metal ions in nitric acid solution

  7. Materials and processes for solar fuel production

    CERN Document Server

    Viswanathan, Balasubramanian; Lee, Jae Sung

    2014-01-01

    This book features different approaches to non-biochemical pathways for solar fuel production. This one-of-a-kind book addresses photovoltaics, photocatalytic water splitting for clean hydrogen production and CO2 conversion to hydrocarbon fuel through in-depth comprehensive contributions from a select blend of established and experienced authors from across the world. The commercial application of solar based systems, with particular emphasis on non-PV based devices have been discussed. This book intends to serve as a primary resource for a multidisciplinary audience including chemists, engineers and scientists providing a one-stop location for all aspects related to solar fuel production. The material is divided into three sections: Solar assisted water splitting to produce hydrogen; Solar assisted CO2 utilization to produce green fuels and Solar assisted electricity generation. The content strikes a balance between theory, material synthesis and application with the central theme being solar fuels.

  8. Photocatalytic oxide films in the built environment

    Science.gov (United States)

    Österlund, Lars; Topalian, Zareh

    2014-11-01

    The possibility to increase human comfort in buildings is a powerful driving force for the introduction of new technology. Among other things our sense of comfort depends on air quality, temperature, lighting level, and the possibility of having visual contact between indoors and outdoors. Indeed there is an intimate connection between energy, comfort, and health issues in the built environment, leading to a need for intelligent building materials and green architecture. Photocatalytic materials can be applied as coatings, filters, and be embedded in building materials to provide self-cleaning, antibacterial, air cleaning, deodorizing, and water cleaning functions utilizing either solar light or artificial illumination sources - either already present in buildings, or by purposefully designed luminaries. Huge improvements in indoor comfort can thus be made, and also alleviate negative health effects associated with buildings, such as the sick-house syndrome. At the same time huge cost savings can be made by reducing maintenance costs. Photocatalytic oxides can be chemically modified by changing their acid-base surface properties, which can be used to overcome deactivation problems commonly encountered for TiO2 in air cleaning applications. In addition, the wetting properties of oxides can be tailored by surface chemical modifications and thus be made e.g. oleophobic and water repellent. Here we show results of surface acid modified TiO2 coatings on various substrates by means of photo-fixation of surface sulfate species by a method invented in our group. In particular, we show that such surface treatments of photocatalytic concrete made by mixing TiO2 nanoparticles in reactive concrete powders result in concrete surfaces with beneficial self-cleaning properties. We propose that such approaches are feasible for a number of applications in the built environment, including glass, tiles, sheet metals, plastics, etc.

  9. Photocatalytic oxide films in the built environment

    International Nuclear Information System (INIS)

    Österlund, Lars; Topalian, Zareh

    2014-01-01

    The possibility to increase human comfort in buildings is a powerful driving force for the introduction of new technology. Among other things our sense of comfort depends on air quality, temperature, lighting level, and the possibility of having visual contact between indoors and outdoors. Indeed there is an intimate connection between energy, comfort, and health issues in the built environment, leading to a need for intelligent building materials and green architecture. Photocatalytic materials can be applied as coatings, filters, and be embedded in building materials to provide self-cleaning, antibacterial, air cleaning, deodorizing, and water cleaning functions utilizing either solar light or artificial illumination sources – either already present in buildings, or by purposefully designed luminaries. Huge improvements in indoor comfort can thus be made, and also alleviate negative health effects associated with buildings, such as the sick-house syndrome. At the same time huge cost savings can be made by reducing maintenance costs. Photocatalytic oxides can be chemically modified by changing their acid-base surface properties, which can be used to overcome deactivation problems commonly encountered for TiO 2 in air cleaning applications. In addition, the wetting properties of oxides can be tailored by surface chemical modifications and thus be made e.g. oleophobic and water repellent. Here we show results of surface acid modified TiO 2 coatings on various substrates by means of photo-fixation of surface sulfate species by a method invented in our group. In particular, we show that such surface treatments of photocatalytic concrete made by mixing TiO 2 nanoparticles in reactive concrete powders result in concrete surfaces with beneficial self-cleaning properties. We propose that such approaches are feasible for a number of applications in the built environment, including glass, tiles, sheet metals, plastics, etc

  10. Solar photocatalytic cleaning of polluted water

    International Nuclear Information System (INIS)

    Bockelmann, D.

    1994-01-01

    Alternatively to biological, physical and chemical methods of waste water cleaning, photocatalysis can be employed. In this residue-free method, titanium dioxide particles are brought into contact with polluted water as photocatalysts. Under UV irradiation at wave-lengths below 400 nm, change carriers are generated in the semiconductor particles that act so intensely oxidizing as to completely degrade almost all organic pollutants in waste water. In this process, the ultra-violet part of the solar spectrum can be harnessed to generate oxidation equivalents. Thus, solar photocatalytic waste water cleaning is excellently suited for developing countries. (BWI) [de

  11. Fuel Exhaling Fuel Cell.

    Science.gov (United States)

    Manzoor Bhat, Zahid; Thimmappa, Ravikumar; Devendrachari, Mruthyunjayachari Chattanahalli; Kottaichamy, Alagar Raja; Shafi, Shahid Pottachola; Varhade, Swapnil; Gautam, Manu; Thotiyl, Musthafa Ottakam

    2018-01-18

    State-of-the-art proton exchange membrane fuel cells (PEMFCs) anodically inhale H 2 fuel and cathodically expel water molecules. We show an unprecedented fuel cell concept exhibiting cathodic fuel exhalation capability of anodically inhaled fuel, driven by the neutralization energy on decoupling the direct acid-base chemistry. The fuel exhaling fuel cell delivered a peak power density of 70 mW/cm 2 at a peak current density of 160 mA/cm 2 with a cathodic H 2 output of ∼80 mL in 1 h. We illustrate that the energy benefits from the same fuel stream can at least be doubled by directing it through proposed neutralization electrochemical cell prior to PEMFC in a tandem configuration.

  12. The Promoting Role of Different Carbon Allotropes Cocatalysts for Semiconductors in Photocatalytic Energy Generation and Pollutants Degradation

    Directory of Open Access Journals (Sweden)

    Weiwei Han

    2017-10-01

    Full Text Available Semiconductor based photocatalytic process is of great potential for solving the fossil fuels depletion and environmental pollution. Loading cocatalysts for the modification of semiconductors could increase the separation efficiency of the photogenerated hole-electron pairs, enhance the light absorption ability of semiconductors, and thus obtain new composite photocatalysts with high activities. Kinds of carbon allotropes, such as activated carbon, carbon nanotubes, graphene, and carbon quantum dots have been used as effective cocatalysts to enhance the photocatalytic activities of semiconductors, making them widely used for photocatalytic energy generation, and pollutants degradation. This review focuses on the loading of different carbon allotropes as cocatalysts in photocatalysis, and summarizes the recent progress of carbon materials based photocatalysts, including their synthesis methods, the typical applications, and the activity enhancement mechanism. Moreover, the cocatalytic effect among these carbon cocatalysts is also compared for different applications. We believe that our work can provide enriched information to harvest the excellent special properties of carbon materials as a platform to develop more efficient photocatalysts for solar energy utilization.

  13. Nano cobalt oxides for photocatalytic hydrogen production

    KAUST Repository

    Mangrulkar, Priti A.

    2012-07-01

    Nano structured metal oxides including TiO 2, Co 3O 4 and Fe 3O 4 have been synthesized and evaluated for their photocatalytic activity for hydrogen generation. The photocatalytic activity of nano cobalt oxide was then compared with two other nano structured metal oxides namely TiO 2 and Fe 3O 4. The synthesized nano cobalt oxide was characterized thoroughly with respect to EDX and TEM. The yield of hydrogen was observed to be 900, 2000 and 8275 mmol h -1 g -1 of photocatalyst for TiO 2, Co 3O 4 and Fe 3O 4 respectively under visible light. It was observed that the hydrogen yield in case of nano cobalt oxide was more than twice to that of TiO 2 and the hydrogen yield of nano Fe 3O 4 was nearly four times as compared to nano Co 3O 4. The influence of various operating parameters in hydrogen generation by nano cobalt oxide was then studied in detail. Copyright © 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

  14. Photocatalytic Water-Splitting Reaction from Catalytic and Kinetic Perspectives

    KAUST Repository

    Hisatomi, Takashi; Takanabe, Kazuhiro; Domen, Kazunari

    2014-01-01

    Abstract: Some particulate semiconductors loaded with nanoparticulate catalysts exhibit photocatalytic activity for the water-splitting reaction. The photocatalysis is distinct from the thermal catalysis because photocatalysis involves photophysical

  15. Oxidative esterification via photocatalytic C-H activation

    Data.gov (United States)

    U.S. Environmental Protection Agency — Direct oxidative esterification of alcohol via photocatalytic C–H activation has been developed using VO@g-C3N4 catalyst; an expeditious esterification of alcohols...

  16. Nano-/microstructure improved photocatalytic activities of semiconductors.

    Science.gov (United States)

    Zhao, Tianyi; Zhao, Yong; Jiang, Lei

    2013-10-13

    Photocatalysis has emerged as a promising technique owing to its valuable applications in environmental purification. With the demand of building effective photocatalyst materials, semiconductor investigation experienced a developing process from simple chemical modification to complicated morphology design. In this review, the general relationship between morphology structures and photocatalytic properties is mainly discussed. Various nano-/microsized structures from zero- to three-dimensional are discussed, and the photocatalytic efficiency correspon- ding to the structures is analysed. The results showed that simple structures can be easily obtained and can facilitate chemical modification, whereas one- or three-dimensional structures can provide structure-enhanced properties such as surface area increase, multiple reflections of UV light, etc. Those principles of structure-related photocatalytic properties will afford basic ideology in designing new photocatalytic materials with more effective catalytic properties.

  17. Water-driven micromotors for rapid photocatalytic degradation of biological and chemical warfare agents.

    Science.gov (United States)

    Li, Jinxing; Singh, Virendra V; Sattayasamitsathit, Sirilak; Orozco, Jahir; Kaufmann, Kevin; Dong, Renfeng; Gao, Wei; Jurado-Sanchez, Beatriz; Fedorak, Yuri; Wang, Joseph

    2014-11-25

    Threats of chemical and biological warfare agents (CBWA) represent a serious global concern and require rapid and efficient neutralization methods. We present a highly effective micromotor strategy for photocatalytic degradation of CBWA based on light-activated TiO2/Au/Mg microspheres that propel autonomously in natural water and obviate the need for external fuel, decontaminating reagent, or mechanical agitation. The activated TiO2/Au/Mg micromotors generate highly reactive oxygen species responsible for the efficient destruction of the cell membranes of the anthrax simulant Bacillus globigii spore, as well as rapid and complete in situ mineralization of the highly persistent organophosphate nerve agents into nonharmful products. The water-driven propulsion of the TiO2/Au/Mg micromotors facilitates efficient fluid transport and dispersion of the photogenerated reactive oxidative species and their interaction with the CBWA. Coupling of the photocatalytic surface of the micromotors and their autonomous water-driven propulsion thus leads to a reagent-free operation which holds a considerable promise for diverse "green" defense and environmental applications.

  18. Preparation and photocatalytic properties of YVO4 nanopowders

    International Nuclear Information System (INIS)

    Xu Haiyan; Wang Hao; Yan Hui

    2007-01-01

    YVO 4 photocatalysts with different grain sizes were obtained by annealing the YVO 4 nanopowders synthesized via microwave irradiation. The products were characterized by X-ray diffractometer (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), surface area and porosity analyzer, and ultraviolet-visible (UV-vis) spectrophotometer. Photocatalytic measurements showed that the YVO 4 nanopowders with grain size of about 5 nm possess superior photocatalytic properties in decolorization of methyl orange solution

  19. Photocatalytic Water Oxidation on ZnO: A Review

    Directory of Open Access Journals (Sweden)

    Sharifah Bee Abdul Hamid

    2017-03-01

    Full Text Available The investigation of the water oxidation mechanism on photocatalytic semiconductor surfaces has gained much attention for its potential to unlock the technological limitations of producing H2 from carbon-free sources, i.e., H2O. This review seeks to highlight the available scientific and fundamental understanding towards the water oxidation mechanism on ZnO surfaces, as well as present a summary on the modification strategies carried out to increase the photocatalytic response of ZnO.

  20. Photocatalytic Degradation of Aniline Using TiO2 Nanoparticles in a Vertical Circulating Photocatalytic Reactor

    Directory of Open Access Journals (Sweden)

    F. Shahrezaei

    2012-01-01

    Full Text Available Photocatalytic degradation of aniline in the presence of titanium dioxide (TiO2 and ultraviolet (UV illumination was performed in a vertical circulating photocatalytic reactor. The effects of catalyst concentration (0–80 mg/L, initial pH (2–12, temperature (293–323 K, and irradiation time (0–120 min on aniline photodegradation were investigated in order to obtain the optimum operational conditions. The results reveal that the aniline degradation efficiency can be effectively improved by increasing pH from 2 to 12 and temperature from 313 to 323 K. Besides, the effect of temperature on aniline photo degradation was found to be unremarkable in the range of 293–313 K. The optimum catalyst concentration was about 60 mg/L. The Langmuir Hinshelwood kinetic model could successfully elucidate the effects of the catalyst concentration, pH, and temperature on the rate of heterogeneous photooxidation of aniline. The data obtained by applying the Langmuir Hinshelwood treatment are consistent with the available kinetic parameters. The activated energy for the photocatalytic degradation of aniline is 20.337 kj/mol. The possibility of the reactor use in the treatment of a real petroleum refinery wastewater was also investigated. The results of the experiments indicated that it can therefore be potentially applied for the treatment of wastewater contaminated by different organic pollutants.

  1. Photocatalytic Water Treatment by Titanium Dioxide: Recent Updates

    Directory of Open Access Journals (Sweden)

    Manoj A. Lazar

    2012-12-01

    Full Text Available Photocatalytic water treatment using nanocrystalline titanium dioxide (NTO is a well-known advanced oxidation process (AOP for environmental remediation. With the in situ generation of electron-hole pairs upon irradiation with light, NTO can mineralize a wide range of organic compounds into harmless end products such as carbon dioxide, water, and inorganic ions. Photocatalytic degradation kinetics of pollutants by NTO is a topic of debate and the mostly reporting Langmuir-Hinshelwood kinetics must accompanied with proper experimental evidences. Different NTO morphologies or surface treatments on NTO can increase the photocatalytic efficiency in degradation reactions. Wisely designed photocatalytic reactors can decrease energy consumption or can avoid post-separation stages in photocatalytic water treatment processes. Doping NTO with metals or non-metals can reduce the band gap of the doped catalyst, enabling light absorption in the visible region. Coupling NTO photocatalysis with other water-treatment technologies can be more beneficial, especially in large-scale treatments. This review describes recent developments in the field of photocatalytic water treatment using NTO.

  2. Activation of glassy carbon electrodes by photocatalytic pretreatment

    Energy Technology Data Exchange (ETDEWEB)

    Dumanli, Onur [Department of Chemistry, Faculty of Science and Art, Ondokuz Mayis University, Kurupelit, 55139 Samsun (Turkey); Onar, A. Nur [Department of Chemistry, Faculty of Science and Art, Ondokuz Mayis University, Kurupelit, 55139 Samsun (Turkey)], E-mail: nonar@omu.edu.tr

    2009-11-01

    This paper describes a simple and rapid photocatalytic pretreatment procedure that removes contaminants from glassy carbon (GC) surfaces. The effectiveness of TiO{sub 2} mediated photocatalytic pretreatment procedure was compared to commonly used alumina polishing procedure. Cyclic voltammetric and chronocoulometric measurements were carried out to assess the changes in electrode reactivity by using four redox systems. Electrochemical measurements obtained on photocatalytically treated GC electrodes showed a more active surface relative to polished GC. In cyclic voltammograms of epinephrine, Fe(CN){sub 6}{sup 3-/4-} and ferrocene redox systems, higher oxidation and reduction currents were observed. The heterogeneous electron transfer rate constants (k{sup o}) were calculated for Fe(CN){sub 6}{sup 3-/4-} and ferrocene which were greater for photocatalytic pretreatment. Chronocoulometry was performed in order to find the amount of adsorbed methylene blue onto the electrode and was calculated as 0.34 pmol cm{sup -2} for photocatalytically pretreated GC. The proposed photocatalytic GC electrode cleansing and activating pretreatment procedure was more effective than classical alumina polishing.

  3. Fuel assemblies

    International Nuclear Information System (INIS)

    Mukai, Hideyuki

    1987-01-01

    Purpose: To prevent bending of fuel rods caused by the difference of irradiation growth between coupling fuel rods and standards fuel rods thereby maintain the fuel rod integrity. Constitution: The f value for a fuel can (the ratio of pole of zirconium crystals in the entire crystals along the axial direction of the fuel can) of a coupling fuel rod secured by upper and lower tie plates is made smaller than the f value for the fuel can of a standard fuel rod not secured by the upper and the lower tie plates. This can make the irradiation growth of the fuel can of the coupling fuel rod greater than the irradiation growth of the fuel can of the standard fuel rod and, accordingly, since the elongation of the standard fuel rod can always by made greater, bending of the standard fuel rod can be prevented. (Yoshihara, M.)

  4. Alternative photocatalysts to TiO{sub 2} for the photocatalytic reduction of CO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Nikokavoura, Aspasia; Trapalis, Christos, E-mail: c.trapalis@inn.demokritos.gr

    2017-01-01

    Highlights: • Non TiO{sub 2} containing photocatalysts are intensively studied for CO{sub 2} reduction. • The inorganic and carbon based semiconductors are appropriate for redox reactions. • ZIFs and carbonaceous hybrids exhibited outstanding photocatalytic efficiency. • Highly active photocatalysts for CO{sub 2} conversion to useful materials are needed. - Abstract: The increased concentration of CO{sub 2} in the atmosphere, originating from the burning of fossil fuels in stationary and mobile sources, is referred as the “Anthropogenic Greenhouse Effect” and constitutes a major environmental concern. The scientific community is highly concerned about the resulting enhancement of the mean atmospheric temperature, so a vast diversity of methods has been applied. Thermochemical, electrochemical, photocatalytic, photoelectrochemical processes, as well as combination of solar electricity generation and water splitting processes have been performed in order to lower the CO{sub 2} atmospheric levels. Photocatalytic methods are environmental friendly and succeed in reducing the atmospheric CO{sub 2} concentration and producing fuels or/and useful organic compounds at the same time. The most common photocatalysts for the CO{sub 2} reduction are the inorganic, the carbon based semiconductors and the hybrids based on semiconductors, which combine stability, low cost and appropriate structure in order to accomplish redox reactions. In this review, inorganic semiconductors such as single-metal oxide, mixed-metal oxides, metal oxide composites, layered double hydroxides (LDHs), salt composites, carbon based semiconductors such as graphene based composites, CNT composites, g-C{sub 3}N{sub 4} composites and hybrid organic-inorganic materials (ZIFs) were studied. TiO{sub 2} and Ti based photocatalysts are extensively studied and therefore in this review they are not mentioned.

  5. The influence of photocatalytic interior paints on indoor air quality

    Science.gov (United States)

    Auvinen, Joonas; Wirtanen, Leif

    2008-06-01

    A clean indoor air is important for the well-being and health of people. Lately, new photocatalytic paints have been launched on the market, which are claimed to have air-purifying effects. Photocatalysis initiates radical reactions. Radicals are formed when a photocatalyst (e.g. TiO2) is subjected to radiation. Typical radicals are the hydroxyl radical (radOH) and the superoxide radical (radO2-). Radicals cause chain reactions, which degrade and decompose organic compounds. The end products of these chain reactions are water and carbon dioxide, if the reactions are fully completed (mineralization). If mineralization does not take place, then a great number of side products can be formed, whose properties are not well understood. The side products of photocatalytic reactions can be permanent and stabile. The decomposition of indoor air impurities on the surface of photocatalytic paints is not obvious. The ability of photocatalytic indoor paints to reduce chemical indoor air impurities is the key issue of this study. Six different paints with different binder systems, such as lime, polyorganic siloxane, silica sol-gel and organic binders, were examined. The experiments were divided into three topics: degradation of an organic binder, photocatalytic decomposition of formaldehyde, and a volatile organic compound (VOC) mixture consisting of five different indoor air VOCs. All tests were carried out in an environmental test chamber under dynamic conditions. The test results indicate that many indoor pollutants are generated under normal- and UVA-light. Typical compounds formed include formaldehyde, acetone, acetaldehyde, etc. A clear decrease of formaldehyde or the VOC mixture concentration was not observed. All possibly generated compounds could not be collected or analyzed in this research project, but the measurements show that photocatalytic reactions do not generate only carbon dioxide and water. Photocatalytic decomposition of indoor air impurities can, however

  6. Thickness Dependent on Photocatalytic Activity of Hematite Thin Films

    Directory of Open Access Journals (Sweden)

    Yen-Hua Chen

    2012-01-01

    Full Text Available Hematite (Fe2O3 thin films with different thicknesses are fabricated by the rf magnetron sputtering deposition. The effects of film thicknesses on the photocatalytic activity of hematite films have been investigated. Hematite films possess a polycrystalline hexagonal structure, and the band gap decreases with an increase of film thickness. Moreover, all hematite films exhibit good photocatalytic ability under visible-light irradiation; the photocatalytic activity of hematite films increases with the increasing film thickness. This is because the hematite film with a thicker thickness has a rougher surface, providing more reaction sites for photocatalysis. Another reason is a lower band gap of a hematite film would generate more electron-hole pairs under visible-light illumination to enhance photocatalytic efficiency. Experimental data are well fitted with Langmuir-Hinshelwood kinetic model. The photocatalytic rate constant of hematite films ranges from 0.052 to 0.068 min-1. This suggests that the hematite film is a superior photocatalyst under visible-light irradiation.

  7. TiO2–AgCl Based Nanoparticles for Photocatalytic Production of Phenolic Compounds from Lignocellulosic Residues

    DEFF Research Database (Denmark)

    Tsapekos, Panagiotis; Alvarado-Morales, Merlin; Boscaro, Davide

    2018-01-01

    Lignocellulosic biomass residues can be used as an interesting resource for the production of biochemicals or sustainable fuels. In this optic, lignin represents an interesting raw material for the production of chemicals, such as aromatic compounds, or fuels. This can contribute in moving away...... for optimal phenolic compounds production. It was found that the photocatalytic treatment boosted the phenolic production from wheat straw. The efficiency of the process depended on the initial pH and catalyst concentration. Process optimization towards increased phenolic compounds production was performed...... of toxic compounds presented in the catalyst-straw solution and specifically, HNO3 was toxic to methanogenic communities. Hence, to succeed in an efficient biorefinery framework where total phenols and biogas production are combined, the usage of HNO3 for catalyst synthesis should be avoided....

  8. [Spectroscopic study of photocatalytic mechanism of methanol and CO2].

    Science.gov (United States)

    Hai, Feng; Zhang, Qian-cheng; Bai, Feng-rong; Wang, A-nan; Wang, Zhi-wei; Jian, Li

    2011-12-01

    Ni-Ti-O/SiO2 catalyst was prepared by impregnation method, and its photocatalytic performance for carbonylation of methanol with CO2 was investigated under UV light. The in-situ IR, XPS and MS were carried out to analyze the possible photocatalytic reaction mechanism. Results indicated that the Ni-Ti-O/SiO2 exhibited good photocatalytic performance for carbonylation of methanol with CO2, the methanol conversion reached up to 24.9%, and the selectivity for the carbonylated products was more than 60% within 180 min reaction time. The catalyst characterization results showed that the O==C .--O- and CH3OC(O)* might be important intermediate in the carbonylation of methanol with CO2.

  9. Tantalum nitride for photocatalytic water splitting: concept and applications

    KAUST Repository

    Nurlaela, Ela; Ziani, Ahmed; Takanabe, Kazuhiro

    2016-01-01

    Along with many other solar energy conversion processes, research on photocatalytic water splitting to generate hydrogen and oxygen has experienced rapid major development over the past years. Developing an efficient visible-light-responsive photocatalyst has been one of the targets of such research efforts. In this regard, nitride materials, particularly Ta3N5, have been the subject of investigation due to their promising properties. This review focuses on the fundamental parameters involved in the photocatalytic processes targeting overall water splitting using Ta3N5 as a model photocatalyst. The discussion primarily focuses on relevant parameters that are involved in photon absorption, exciton separation, carrier diffusion, carrier transport, catalytic efficiency, and mass transfer of the reactants. An overview of collaborative experimental and theoretical approaches to achieve efficient photocatalytic water splitting using Ta3N5 is discussed.

  10. Characterizing Nanoparticles Reactivity: Structure-Photocatalytic Activity Relationship

    International Nuclear Information System (INIS)

    Piella, J; Bastús, N G; Casals, E; Puntes, V

    2013-01-01

    Nanoparticles are reactive, and their final interactions with the surrounding media are ultimately determined by their reactivity, which in turns depends on the nanoparticles morphology, surface chemistry and environment in which they are embedded. One simple and informative approach for the study of the reactivity of nanoparticles is the determination of their photocatalytic activity. In the present work, we briefly summarize the importance of different parameters such as the size, shape and agglomeration state on the photocatalytic activity of colloidal inorganic nanoparticles. The study of the use of nanoparticles as photocatalyts is relevant not only for its potential applications in environmental remediation issues but also it can provide relevant information about the role of these parameters at the nanoscale.

  11. Tantalum nitride for photocatalytic water splitting: concept and applications

    KAUST Repository

    Nurlaela, Ela

    2016-10-12

    Along with many other solar energy conversion processes, research on photocatalytic water splitting to generate hydrogen and oxygen has experienced rapid major development over the past years. Developing an efficient visible-light-responsive photocatalyst has been one of the targets of such research efforts. In this regard, nitride materials, particularly Ta3N5, have been the subject of investigation due to their promising properties. This review focuses on the fundamental parameters involved in the photocatalytic processes targeting overall water splitting using Ta3N5 as a model photocatalyst. The discussion primarily focuses on relevant parameters that are involved in photon absorption, exciton separation, carrier diffusion, carrier transport, catalytic efficiency, and mass transfer of the reactants. An overview of collaborative experimental and theoretical approaches to achieve efficient photocatalytic water splitting using Ta3N5 is discussed.

  12. Light energy conversion by photocatalytic reaction

    Energy Technology Data Exchange (ETDEWEB)

    Fujishima, Akira; Yamagata, Sadamu [Univ. of Tokyo (Japan)

    1989-01-01

    The photocatalytic reaction, to be made to a suspended semiconductor powder system, was explained in summary. By using semiconductor as an electrode for the electrolyzation, etc. and projecting light on it to generate photoelectromotive force, a photocell can be composed. eg., by composing titanium oxide electrode, n-type semiconductor and platinum electrode, and irradiating light on the former electrode to generate electric current, oxygen and hydrogen are produced from the titanium oxide electrode and platinum electrode, respectively, which means the possibility of obtainment of clean energy from water as raw material. Such a wet type photocell, easy to produce, is active also in research. With white titanium oxide powder being suspended in water solution, hydrogen is produced by projecting light into it. Such a semiconductor is called photocatalyst, in which the research has been widely developed, mainly by taking notice of the hydrogen production on reduction side, since 1972. The photocatalysis using colloid and, differently, that doing heteropolyacid are also taken notice of. 24 refs., 6 figs.

  13. Quasiparticle Level Alignment for Photocatalytic Interfaces.

    Science.gov (United States)

    Migani, Annapaoala; Mowbray, Duncan J; Zhao, Jin; Petek, Hrvoje; Rubio, Angel

    2014-05-13

    Electronic level alignment at the interface between an adsorbed molecular layer and a semiconducting substrate determines the activity and efficiency of many photocatalytic materials. Standard density functional theory (DFT)-based methods have proven unable to provide a quantitative description of this level alignment. This requires a proper treatment of the anisotropic screening, necessitating the use of quasiparticle (QP) techniques. However, the computational complexity of QP algorithms has meant a quantitative description of interfacial levels has remained elusive. We provide a systematic study of a prototypical interface, bare and methanol-covered rutile TiO2(110) surfaces, to determine the type of many-body theory required to obtain an accurate description of the level alignment. This is accomplished via a direct comparison with metastable impact electron spectroscopy (MIES), ultraviolet photoelectron spectroscopy (UPS), and two-photon photoemission (2PP) spectroscopy. We consider GGA DFT, hybrid DFT, and G0W0, scQPGW1, scQPGW0, and scQPGW QP calculations. Our results demonstrate that G0W0, or our recently introduced scQPGW1 approach, are required to obtain the correct alignment of both the highest occupied and lowest unoccupied interfacial molecular levels (HOMO/LUMO). These calculations set a new standard in the interpretation of electronic structure probe experiments of complex organic molecule/semiconductor interfaces.

  14. Novel Solar Photocatalytic Reactor for Wastewater Treatment

    Science.gov (United States)

    Sutisna; Rokhmat, M.; Wibowo, E.; Murniati, R.; Khairurrijal; Abdullah, M.

    2017-07-01

    A new solar photocatalytic reactor (photoreactor) using TiO2 nanoparticles coated onto plastic granules has been designed. Catalyst granules are placed into the cavity of a reactor panel made of glass. A pump is used to circulate wastewater in the photoreactor. Methylene blue (MB) dissolved in water was chosen as the wastewater model. The performance of the photoreactor was evaluated based on changes in MB concentration with respect to time. The photoreactor showed a good performance by degrading 10 L of MB solution up to 96.54% after 48 h of solar irradiation. The photoreactor was scaled up by enlarging the panel area to twice its original size. The increase in the surface area of the reactor panel and therefore of the mass of catalyst granules and reactor volume led to a three-fold increase of the photodegradation rate. In addition, the MB degradation kinetics were also studied. Data analysis confirmed the applicability of the pseudo-first-order Langmuir-Hinshelwood model. The proposed photoreactor has great potential for use in large-scale wastewater treatment.

  15. Photocatalytic surface reactions on indoor wall paint.

    Science.gov (United States)

    Salthammer, T; Fuhrmann, F

    2007-09-15

    The reduction of indoor air pollutants by air cleaning systems has received considerable interest, and a number of techniques are now available. So far, the method of photocatalysis was mainly applied by use of titanium dioxide (TiO2) in flow reactors under UV light of high intensity. Nowadays, indoor wall paints are equipped with modified TiO2 to work as a catalyst under indoor daylight or artificial light. In chamber experiments carried out under indoor related conditions itwas shown thatthe method works for nitrogen dioxide with air exchange and for formaldehyde without air exchange at high concentrations. In further experiments with volatile organic compounds (VOCs), a small effect was found for terpenoids with high kOH rate constants. For other VOCs and carbon monoxide there was no degradation at all or the surface acted as a reversible sink. Secondary emissions from the reaction of paint constituents were observed on exposure to light. From the results it is concluded that recipes of photocatalytic wall paints need to be optimized for better efficiency under indoor conditions.

  16. Alternative Fuels

    Science.gov (United States)

    Alternative fuels include gaseous fuels such as hydrogen, natural gas, and propane; alcohols such as ethanol, methanol, and butanol; vegetable and waste-derived oils; and electricity. Overview of alternative fuels is here.

  17. Understanding Mechanism of Photocatalytic Microbial Decontamination of Environmental Wastewater

    Directory of Open Access Journals (Sweden)

    Chhabilal Regmi

    2018-02-01

    Full Text Available Several photocatalytic nanoparticles are synthesized and studied for potential application for the degradation of organic and biological wastes. Although these materials degrade organic compounds by advance oxidation process, the exact mechanisms of microbial decontamination remains partially known. Understanding the real mechanisms of these materials for microbial cell death and growth inhibition helps to fabricate more efficient semiconductor photocatalyst for large-scale decontamination of environmental wastewater or industries and hospitals/biomedical labs generating highly pathogenic bacteria and toxic molecules containing liquid waste by designing a reactor. Recent studies on microbial decontamination by photocatalytic nanoparticles and their possible mechanisms of action is highlighted with examples in this mini review.

  18. Fuel assembly

    International Nuclear Information System (INIS)

    Chaki, Masao; Nishida, Koji; Karasawa, Hidetoshi; Kanazawa, Toru; Orii, Akihito; Nagayoshi, Takuji; Kashiwai, Shin-ichi; Masuhara, Yasuhiro

    1998-01-01

    The present invention concerns a fuel assembly, for a BWR type nuclear reactor, comprising fuel rods in 9 x 9 matrix. The inner width of the channel box is about 132mm and the length of the fuel rods which are not short fuel rods is about 4m. Two water rods having a circular cross section are arranged on a diagonal line in a portion of 3 x 3 matrix at the center of the fuel assembly, and two fuel rods are disposed at vacant spaces, and the number of fuel rods is 74. Eight fuel rods are determined as short fuel rods among 74 fuel rods. Assuming the fuel inventory in the short fuel rod as X(kg), and the fuel inventory in the fuel rods other than the short fuel rods as Y(kg), X and Y satisfy the relation: X + Y ≥ 173m, Y ≤ - 9.7X + 292, Y ≤ - 0.3X + 203 and X > 0. Then, even when the short fuel rods are used, the fuel inventory is increased and fuel economy can be improved. (I.N.)

  19. Fuel assembly

    International Nuclear Information System (INIS)

    Yamazaki, Hajime.

    1995-01-01

    In a fuel assembly having fuel rods of different length, fuel pellets of mixed oxides of uranium and plutonium are loaded to a short fuel rod. The volume ratio of a pellet-loaded portion to a plenum portion of the short fuel rod is made greater than the volume ratio of a fuel rod to which uranium fuel pellets are loaded. In addition, the volume of the plenum portion of the short fuel rod is set greater depending on the plutonium content in the loaded fuel pellets. MOX fuel pellets are loaded on the short fuel rods having a greater degree of freedom relevant to the setting for the volume of the plenum portion compared with that of a long rod fuel, and the volume of the plenum portion is ensured greater depending on the plutonium content. Even if a large amount of FP gas and He gas are discharged from the MOX fuels compared with that from the uranium fuels, the internal pressure of the MOX fuel rod during operation is maintained substantially identical with that of the uranium fuel rod, so that a risk of generating excess stresses applied to the fuel cladding tubes and rupture of fuels are greatly reduced. (N.H.)

  20. Nuclear fuels

    International Nuclear Information System (INIS)

    Gangwani, Saloni; Chakrabortty, Sumita

    2011-01-01

    Nuclear fuel is a material that can be consumed to derive nuclear energy, by analogy to chemical fuel that is burned for energy. Nuclear fuels are the most dense sources of energy available. Nuclear fuel in a nuclear fuel cycle can refer to the fuel itself, or to physical objects (for example bundles composed of fuel rods) composed of the fuel material, mixed with structural, neutron moderating, or neutron reflecting materials. Long-lived radioactive waste from the back end of the fuel cycle is especially relevant when designing a complete waste management plan for SNF. When looking at long-term radioactive decay, the actinides in the SNF have a significant influence due to their characteristically long half-lives. Depending on what a nuclear reactor is fueled with, the actinide composition in the SNF will be different. The following paper will also include the uses. advancements, advantages, disadvantages, various processes and behavior of nuclear fuels

  1. Fuel and nuclear fuel cycle

    International Nuclear Information System (INIS)

    Prunier, C.

    1998-01-01

    The nuclear fuel is studied in detail, the best choice and why in relation with the type of reactor, the properties of the fuel cans, the choice of fuel materials. An important part is granted to the fuel assembly of PWR type reactor and the performances of nuclear fuels are tackled. The different subjects for research and development are discussed and this article ends with the particular situation of mixed oxide fuels ( materials, behavior, efficiency). (N.C.)

  2. Photocatalytic treatment of bioaerosols: impact of the reactor design.

    Science.gov (United States)

    Josset, Sébastien; Taranto, Jérôme; Keller, Nicolas; Keller, Valérie; Lett, Marie-Claire

    2010-04-01

    Comparing the UV-A photocatalytic treatment of bioaerosols contaminated with different airborne microorganisms such as L. pneumophila bacteria, T2 bacteriophage viruses and B. atrophaeus bacterial spores, pointed out a decontamination sensitivity following the bacteria > virus > bacterial spore ranking order, differing from that obtained for liquid-phase or surface UV-A photocatalytic disinfection. First-principles CFD investigation applied to a model annular photoreactor evidenced that larger the microorganism size, higher the hit probability with the photocatalytic surfaces. Applied to a commercial photocatalytic purifier case-study, the CFD calculations showed that the performances of the studied purifier could strongly benefit from rational reactor design engineering. The results obtained highlighted the required necessity to specifically investigate the removal of airborne microorganisms in terms of reactor design, and not to simply transpose the results obtained from studies performed toward chemical pollutants, especially for a successful commercial implementation of air decontamination photoreactors. This illustrated the importance of the aerodynamics in air decontamination, directly resulting from the microorganism morphology.

  3. Structural, magnetic and photocatalytic characterization of Bi1 ...

    Indian Academy of Sciences (India)

    47

    The UV–Vis absorption spectra were recorded on a Shimadzu UV-Vis-52550 spectrophotometer with the wavelength range of 200–700 nm. Photocatalytic activity of the synthesized Bi1-xLaxFeO3 nanoparticles was evaluated by the degradation of methylene blue (MB) in aqueous solution under visible light radiation.

  4. Flexible substrates as basis for photocatalytic reduction of carbon dioxide

    DEFF Research Database (Denmark)

    Jensen, Jacob; Mikkelsen, Mette; Krebs, Frederik C

    2011-01-01

    A photocatalytic system for converting carbon dioxide into carbon monoxide was designed and constructed. The system relies on thin films of the photocatalyst prepared at low temperature using spray coating. We formulated inks based on the well-known photocatalyst titanium dioxide and characterized...

  5. Characterization and photocatalytic activity of Barkin-Ladi ilmenite ...

    African Journals Online (AJOL)

    Photocatalysis is an advanced oxidation process that can be carried out at room temperature under atmospheric pressure using atmospheric oxygen as the oxidant and the sun as the source of energy. This work focuses on the composition and photocatalytic activity of the raw and calcined samples of ilmenite ore obtained ...

  6. Enhanced photocatalytic properties in well-ordered mesoporous WO3

    KAUST Repository

    Li, Li; Krissanasaeranee, Methira; Pattinson, Sebastian W.; Stefik, Morgan; Wiesner, Ulrich; Steiner, Ullrich; Eder, Dominik

    2010-01-01

    We used polyisoprene-block-ethyleneoxide copolymers as structure-directing agents to synthesise well-ordered and highly-crystalline mesoporous WO 3 architectures that possess improved photocatalytic properties due to enhanced dye-adsorption in absence of diffusion limitation. © 2010 The Royal Society of Chemistry.

  7. Employing RADIANCE to refine indoor photocatalytic oxidation modeling

    NARCIS (Netherlands)

    Pelzers, R.S.; Yu, Q.; Mangkuto, R.A.; Brouwers, H.J.H.

    2013-01-01

    Indoor air quality (IAQ) gained great attention in the last years as one of the foremost environmental concerns and it is therefore imperative that effective methods are developed to conserve IAQ. Currently, the novel technology photocatalytic oxidation (PCO) is a potential alternative. A

  8. Visible light induced photocatalytic degradation of some xanthene ...

    African Journals Online (AJOL)

    Photocatalytic degradation of eosin and erythrosin-B (xanthene dyes) has been carried out using anthracene semiconductor immobilized on polyethylene films. Effect of various parameters like pH, concentration of dyes, amount of semiconductor and light intensity have been studied on the rate of reaction. Various control ...

  9. A short review on photocatalytic degradation of formaldehyde

    NARCIS (Netherlands)

    Tasbihi, M.; Bendyna, J.K.; Notten, P.H.L.; Hintzen, H.T.J.M.

    2015-01-01

    Nowadays, it is a great challenge to eliminate toxic and harmful organic pollutants from air and water. This paper reviews the role of TiO2 as a photocatalyst, light source and photoreactor in the particular case of removal of formaldehyde using the photocatalytic reaction by titanium dioxide (TiO2

  10. TiO₂-Based Photocatalytic Geopolymers for Nitric Oxide Degradation.

    Science.gov (United States)

    Strini, Alberto; Roviello, Giuseppina; Ricciotti, Laura; Ferone, Claudio; Messina, Francesco; Schiavi, Luca; Corsaro, Davide; Cioffi, Raffaele

    2016-06-24

    This study presents an experimental overview for the development of photocatalytic materials based on geopolymer binders as catalyst support matrices. Particularly, geopolymer matrices obtained from different solid precursors (fly ash and metakaolin), composite systems (siloxane-hybrid, foamed hybrid), and curing temperatures (room temperature and 60 °C) were investigated for the same photocatalyst content (i.e., 3% TiO₂ by weight of paste). The geopolymer matrices were previously designed for different applications, ranging from insulating (foam) to structural materials. The photocatalytic activity was evaluated as NO degradation in air, and the results were compared with an ordinary Portland cement reference. The studied matrices demonstrated highly variable photocatalytic performance depending on both matrix constituents and the curing temperature, with promising activity revealed by the geopolymers based on fly ash and metakaolin. Furthermore, microstructural features and titania dispersion in the matrices were assessed by scanning electron microscopy (SEM) and energy dispersive X-ray (EDS) analyses. Particularly, EDS analyses of sample sections indicated segregation effects of titania in the surface layer, with consequent enhancement or depletion of the catalyst concentration in the active sample region, suggesting non-negligible transport phenomena during the curing process. The described results demonstrated that geopolymer binders can be interesting catalyst support matrices for the development of photocatalytic materials and indicated a large potential for the exploitation of their peculiar features.

  11. Enhancement of visible light irradiation photocatalytic activity of ...

    Indian Academy of Sciences (India)

    Mohamed Abdel Salam

    2017-09-25

    Sep 25, 2017 ... Pt/SrTiO3 nanoparticles for the photocatalytic oxidation of cyclohexane was examined and the results ... Oil and natural gas contain many different compounds .... photoreactor was used. ... doping SrTiO3nanoparticles with Pt do not significantly .... Liu S, Liu Z and Kawi S 1998 Liquid-phase oxidation.

  12. Photo-catalytic Removal of Methyl Orange Dye by Polyaniline ...

    African Journals Online (AJOL)

    Photo-catalytic Removal of Methyl Orange Dye by Polyaniline Modified ZnO using Visible Radiation. ... The as-synthesized nano-ZnO, PANI and PANI/ZnO nanocomposite were characterized by X-ray diffraction (XRD), FT-IR, and UV-Vis spectroscopy. The UV–visible spectroscopy studies showed that the absorption peak ...

  13. Reusable photocatalytic titanium dioxide-cellulose nanofiber films

    Science.gov (United States)

    Alexandra Snyder; Zhenyu Bo; Robert Moon; Jean-Christophe Rochet; Lia. Stanciu

    2013-01-01

    Titanium dioxide (TiO2) is a well-studied photocatalyst that is known to break down organic molecules upon ultraviolet (UV) irradiation. Cellulose nanofibers (CNFs) act as an attractive matrix material for the suspension of photocatalytic particles due to their desirable mechanical and optical properties. In this work, TiO2...

  14. NOx photocatalytic degradation employing concrete pavement containing titanium dioxide

    NARCIS (Netherlands)

    Ballari, M.M.; Hunger, Martin; Hüsken, Götz; Brouwers, Jos

    2010-01-01

    In the present work the degradation of nitrogen oxides (NOx) by concrete paving stones containing TiO2 to be applied in road construction is studied. A kinetic model is proposed to describe the photocatalytic reaction of NOx (combining the degradation of NO and the appearance and disappearance of

  15. Fuel assembly

    International Nuclear Information System (INIS)

    Sakuyama, Tadashi; Mukai, Hideyuki.

    1988-01-01

    Purpose: To prevent the bending of a fuel rod caused by the difference in the elongation between a joined fuel rod and a standard fuel rod thereby maintain the fuel rod integrity. Constitution: A joined fuel rod is in a thread engagement at its lower end plug thereof with a lower plate, while passed through at its upper end plug into an upper tie plate and secured with a nut. Further, a standard fuel rod is engaged at its upper end plug and lower end plug with the upper tie plate and the lower tie plate respectively. Expansion springs are mounted to the upper end plugs of these bonded fuel rods and the standard fuel rods for preventing this lifting. Each of the fuel rods comprises a plurality of sintered pellets of nuclear fuel materials laminated in a zircaloy fuel can. The content of the alloy ingredient in the fuel can of the bonded fuel rod is made greater than that of the alloy ingredient of the standard fuel rod. this can increase the elongation for the bonded fuel rod, and the spring of the standard fuel rod is tightly bonded to prevent the bending. (Yoshino, Y.)

  16. Bio-inspired route for the synthesis of spherical shaped MgO:Fe(3+) nanoparticles: Structural, photoluminescence and photocatalytic investigation.

    Science.gov (United States)

    Anilkumar, M R; Nagaswarupa, H P; Nagabhushana, H; Sharma, S C; Vidya, Y S; Anantharaju, K S; Prashantha, S C; Shivakuamra, C; Gurushantha, K

    2015-01-01

    MgO:Fe(3+) (0.1-5 mol%) nanoparticles (NPs) were synthesized via eco-friendly, inexpensive and simple low temperature solution combustion route using Aloe vera gel as fuel. The final products were characterized by SEM, TEM and HRTEM. PXRD data and Rietveld analysis revealed the formation of cubic system. The influence of Fe(3+) ion concentration on the structure morphology, UV absorption, PL emission and photocatalytic activity of MgO:Fe(3+) NPs were investigated. The yellow emission with CIE chromaticity coordinates (0.44, 0.52) and average correlated color temperature value was found to be 3540 K which corresponds to warm light of NPs. The control of Fe(3+) on MgO matrix influences the photocatalytic decolorization of methylene blue (MB) under UV light. The enhanced photocatalytic activity of MgO:Fe(3+) (4 mol%) was attributed to dopant concentration, effective crystallite size, textural properties, decreased band gap and capability for reducing the electron-hole pair recombination. Further, the trends of inhibitory effect in the presence of different radical scavengers were explored. These findings open up new avenues for the exploration of Fe-doped MgO in eco-friendly water applications and in the process of display devices. Copyright © 2015 Elsevier B.V. All rights reserved.

  17. Self-assembled hierarchical direct Z-scheme g-C3N4/ZnO microspheres with enhanced photocatalytic CO2 reduction performance

    Science.gov (United States)

    Nie, Ning; Zhang, Liuyang; Fu, Junwei; Cheng, Bei; Yu, Jiaguo

    2018-05-01

    Photocatalytic reduction of CO2 into hydrocarbon fuels has been regarded as a promising approach to ease the greenhouse effect and the energy shortage. Herein, an electrostatic self-assembly method was exploited to prepare g-C3N4/ZnO composite microsphere. This method simply utilized the opposite surface charge of each component, achieving a hierarchical structure with intimate contact between them. A much improved photocatalytic CO2 reduction activity was attained. The CH3OH production rate was 1.32 μmol h-1 g-1, which was 2.1 and 4.1 times more than that of the pristine ZnO and g-C3N4, respectively. This facile design bestowed the g-C3N4/ZnO composite an extended light adsorption caused by multi-light scattering effect. It also guaranteed the uniform distribution of g-C3N4 nanosheets on the surface of ZnO microspheres, maximizing their advantage and synergistic effect. Most importantly, the preeminent performance was proposed and validated based on the direct Z-scheme. The recombination rate was considerably suppressed. This work features the meliority of constructing hierarchical direct Z-scheme structures in photocatalytic CO2 reduction reactions.

  18. Fuel processing

    International Nuclear Information System (INIS)

    Allardice, R.H.

    1990-01-01

    The technical and economic viability of the fast breeder reactor as an electricity generating system depends not only upon the reactor performance but also on a capability to recycle plutonium efficiently, reliably and economically through the reactor and fuel cycle facilities. Thus the fuel cycle is an integral and essential part of the system. Fuel cycle research and development has focused on demonstrating that the challenging technical requirements of processing plutonium fuel could be met and that the sometimes conflicting requirements of the fuel developer, fuel fabricator and fuel reprocessor could be reconciled. Pilot plant operation and development and design studies have established both the technical and economic feasibility of the fuel cycle but scope for further improvement exists through process intensification and flowsheet optimization. These objectives and the increasing processing demands made by the continuing improvement to fuel design and irradiation performance provide an incentive for continuing fuel cycle development work. (author)

  19. Experimental study of photocatalytic concrete products for air purification

    Energy Technology Data Exchange (ETDEWEB)

    Huesken, G.; Hunger, M.; Brouwers, H.J.H. [Department of Civil Engineering, Faculty of Engineering Technology, University of Twente, P.O. Box 217, 7500 AE Enschede (Netherlands)

    2009-12-15

    Air quality in inner-city areas is a topic which receives much attention nowadays but in the coming years, the overall interest on this topic will become even bigger. One major concern is caused by the reduction of the limiting values given by the European Council Directive 1999/30/EC [Relating to limit values for sulphur dioxide, nitrogen dioxide and oxides of nitrogen, particulate matter and lead in ambient air. Official Journal of the European Communities 1999, L 163/41-60] and increasing traffic rates especially for diesel powered passenger cars and freight vehicles. A promising approach for solving the problem of nitrogen oxides (NO{sub x}) is the photochemical conversion of nitrogen oxides to low concentrated nitrates due to heterogeneous photocatalytic oxidation (PCO) using titanium dioxide (TiO{sub 2}) as photocatalyst. A variety of products containing TiO{sub 2} are already available on the European market and their working mechanism under laboratory conditions is proven. However, there is still a lack of transforming the experimental results obtained under laboratory conditions to practical applications considering real world conditions. This paper presents the research conducted on photocatalytic concrete products with respect to the evaluation of air-purifying properties. The degradation process of nitric oxide (NO) under laboratory conditions is studied using a test setup for measuring the performance of photocatalytic active concrete products. The test setup uses the UV-A induced degradation of NO and is oriented on the ISO standard ISO 22197-1:2007. Besides the introduction of the test setup, a uniform measuring procedure is presented to the reader which allows for an evaluation and direct comparison of the performance of photocatalytic active concrete products. This kind of direct comparison was not possible so far. Furthermore, the results of a comparative study on varying photocatalytic concrete products of the European market will be discussed

  20. Atom beam sputtered Ag-TiO{sub 2} plasmonic nanocomposite thin films for photocatalytic applications

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Jaspal; Sahu, Kavita [School of Basic and Applied Sciences, Guru Gobind Singh Indraprastha University, Dwarka, NewDelhi 110078 (India); Pandey, A. [Solid State Physics Laboratory, Defence Research and Development Organization, Timarpur, Delhi 110054 (India); Kumar, Mohit [Institute of Physics, Sachivalaya Marg, Bhubaneswar, Odisha 751005 (India); Ghosh, Tapas; Satpati, B. [Saha Institute of Nuclear Physics, HBNI, 1/AF, Bidhannagar, Kolkata 700064 (India); Som, T.; Varma, S. [Institute of Physics, Sachivalaya Marg, Bhubaneswar, Odisha 751005 (India); Avasthi, D.K. [Amity Institute of Nanotechnology, Noida 201313, Uttar Pradesh (India); Mohapatra, Satyabrata, E-mail: smiuac@gmail.com [School of Basic and Applied Sciences, Guru Gobind Singh Indraprastha University, Dwarka, NewDelhi 110078 (India)

    2017-07-31

    The development of nanocomposite coatings with highly enhanced photocatalytic activity is important for photocatalytic purification of water and air. We report on the synthesis of Ag-TiO{sub 2} nanocomposite thin films with highly enhanced photocatalytic activity by atom beam co-sputtering technique. The effects of Ag concentration on the structural, morphological, optical, plasmonic and photocatalytic properties of the nanocomposite thin films were investigated. UV–visible DRS studies revealed the presence of surface plasmon resonance (SPR) peak characteristic of Ag nanoparticles together with the excitonic absorption peak originating from TiO{sub 2} nanoparticles in the nanocomposites. XRD studies showed that the nanocomposite thin films consist of Ag nanoparticles and rutile TiO{sub 2} nanoparticles. The synthesized Ag-TiO{sub 2} nanocomposite thin films with 5 at% Ag were found to exhibit highly enhanced photocatalytic activity for sun light driven photocatalytic degradation of methylene blue in water, indicating their potential application in water purification.

  1. Ni-Nanocluster Modified Black TiO2 with Dual Active Sites for Selective Photocatalytic CO2 Reduction.

    Science.gov (United States)

    Billo, Tadesse; Fu, Fang-Yu; Raghunath, Putikam; Shown, Indrajit; Chen, Wei-Fu; Lien, Hsiang-Ting; Shen, Tzu-Hsien; Lee, Jyh-Fu; Chan, Ting-Shan; Huang, Kuo-You; Wu, Chih-I; Lin, M C; Hwang, Jih-Shang; Lee, Chih-Hao; Chen, Li-Chyong; Chen, Kuei-Hsien

    2018-01-01

    One of the key challenges in artificial photosynthesis is to design a photocatalyst that can bind and activate the CO 2 molecule with the smallest possible activation energy and produce selective hydrocarbon products. In this contribution, a combined experimental and computational study on Ni-nanocluster loaded black TiO 2 (Ni/TiO 2[Vo] ) with built-in dual active sites for selective photocatalytic CO 2 conversion is reported. The findings reveal that the synergistic effects of deliberately induced Ni nanoclusters and oxygen vacancies provide (1) energetically stable CO 2 binding sites with the lowest activation energy (0.08 eV), (2) highly reactive sites, (3) a fast electron transfer pathway, and (4) enhanced light harvesting by lowering the bandgap. The Ni/TiO 2[Vo] photocatalyst has demonstrated highly selective and enhanced photocatalytic activity of more than 18 times higher solar fuel production than the commercial TiO 2 (P-25). An insight into the mechanisms of interfacial charge transfer and product formation is explored. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Photocatalytic Conversion of CO2 to CO using Rhenium Bipyridine Platforms Containing Ancillary Phenyl or BODIPY Moieties

    Science.gov (United States)

    Andrade, Gabriel A.; Pistner, Allen J.; Yap, Glenn P.A.; Lutterman, Daniel A.; Rosenthal, Joel

    2013-01-01

    Harnessing of solar energy to drive the reduction of carbon dioxide to fuels requires the development of efficient catalysts that absorb sunlight. In this work, we detail the synthesis, electrochemistry and photophysical properties of a set of homologous fac-ReI(CO)3 complexes containing either an ancillary phenyl (8) or BODIPY (12) substituent. These studies demonstrate that both the electronic properties of the rhenium center and BODIPY chromophore are maintained for these complexes. Photolysis studies demonstrate that both assemblies 8 and 12 are competent catalysts for the photochemical reduction of CO2 to CO in DMF using triethanolamine (TEOA) as a sacrificial reductant. Both compounds 8 and 12 display TOFs for photocatalytic CO production upon irradiation with light (λex ≥ 400 nm) of ~5 hr−1 with TON values of approximately 20. Although structural and photophysical measurements demonstrate that electronic coupling between the BODIPY and fac-ReI(CO)3 units is limited for complex 12, this work clearly shows that the photoactive BODIPY moiety is tolerated during catalysis and does not interfere with the observed photochemistry. When taken together, these results provide a clear roadmap for the development of advanced rhenium bipyridine complexes bearing ancillary BODIPY groups for the efficient photocatalytic reduction of CO2 using visible light. PMID:24015374

  3. 1D Bi2S3 nanorod/2D e-WS2 nanosheet heterojunction photocatalyst for enhanced photocatalytic activity

    Science.gov (United States)

    Vattikuti, S. V. Prabhakar; Shim, Jaesool; Byon, Chan

    2018-02-01

    The development of high-activity, long-life, precious-metal-free photocatalysts for redox reactions in photoelectrochemical cells and fuel cells remains challenging. The synthesis of high-activity heterostructured photocatalysts is crucial for efficient energy conversion strategies. Herein, a novel photocatalyst based on 1D Bi2S3 nanorods self-assembled on 2D exfoliated tungsten disulfide (e-WS2) nanosheets has been developed for the degradation of methyl orange (MO) dye in aqueous solution. We demonstrate a novel and facile hydrothermal method for the synthesis of a Bi2S3 nanorod/e-WS2 nanosheet heterostructure. The photocatalytic properties of the heterostructure under visible light were investigated. Enhanced photocatalytic activity was attributed to the presence of strong surface active sites, as well as the specific morphology of the composite. We also observed the fast transfer of electron-hole pairs at the material interface. This work demonstrates a non-noble semiconductor photocatalyst for the degradation of pollutants and evolution of H2.

  4. Nuclear fuels

    International Nuclear Information System (INIS)

    Beauvy, M.; Berthoud, G.; Defranceschi, M.; Ducros, G.; Guerin, Y.; Limoge, Y.; Madic, Ch.; Santarini, G.; Seiler, J.M.; Sollogoub, P.; Vernaz, E.; Guillet, J.L.; Ballagny, A.; Bechade, J.L.; Bonin, B.; Brachet, J.Ch.; Delpech, M.; Dubois, S.; Ferry, C.; Freyss, M.; Gilbon, D.; Grouiller, J.P.; Iracane, D.; Lansiart, S.; Lemoine, P.; Lenain, R.; Marsault, Ph.; Michel, B.; Noirot, J.; Parrat, D.; Pelletier, M.; Perrais, Ch.; Phelip, M.; Pillon, S.; Poinssot, Ch.; Vallory, J.; Valot, C.; Pradel, Ph.; Bonin, B.; Bouquin, B.; Dozol, M.; Lecomte, M.; Vallee, A.; Bazile, F.; Parisot, J.F.; Finot, P.; Roberts, J.F.

    2009-01-01

    Fuel is one of the essential components in a reactor. It is within that fuel that nuclear reactions take place, i.e. fission of heavy atoms, uranium and plutonium. Fuel is at the core of the reactor, but equally at the core of the nuclear system as a whole. Fuel design and properties influence reactor behavior, performance, and safety. Even though it only accounts for a small part of the cost per kilowatt-hour of power provided by current nuclear power plants, good utilization of fuel is a major economic issue. Major advances have yet to be achieved, to ensure longer in-reactor dwell-time, thus enabling fuel to yield more energy; and improve ruggedness. Aside from economics, and safety, such strategic issues as use of plutonium, conservation of resources, and nuclear waste management have to be addressed, and true technological challenges arise. This Monograph surveys current knowledge regarding in-reactor behavior, operating limits, and avenues for R and D. It also provides illustrations of ongoing research work, setting out a few noteworthy results recently achieved. Content: 1 - Introduction; 2 - Water reactor fuel: What are the features of water reactor fuel? 9 (What is the purpose of a nuclear fuel?, Ceramic fuel, Fuel rods, PWR fuel assemblies, BWR fuel assemblies); Fabrication of water reactor fuels (Fabrication of UO 2 pellets, Fabrication of MOX (mixed uranium-plutonium oxide) pellets, Fabrication of claddings); In-reactor behavior of UO 2 and MOX fuels (Irradiation conditions during nominal operation, Heat generation, and removal, The processes involved at the start of irradiation, Fission gas behavior, Microstructural changes); Water reactor fuel behavior in loss of tightness conditions (Cladding, the first containment barrier, Causes of failure, Consequences of a failure); Microscopic morphology of fuel ceramic and its evolution under irradiation; Migration and localization of fission products in UOX and MOX matrices (The ceramic under irradiation

  5. Nuclear fuels

    Energy Technology Data Exchange (ETDEWEB)

    Beauvy, M.; Berthoud, G.; Defranceschi, M.; Ducros, G.; Guerin, Y.; Limoge, Y.; Madic, Ch.; Santarini, G.; Seiler, J.M.; Sollogoub, P.; Vernaz, E.; Guillet, J.L.; Ballagny, A.; Bechade, J.L.; Bonin, B.; Brachet, J.Ch.; Delpech, M.; Dubois, S.; Ferry, C.; Freyss, M.; Gilbon, D.; Grouiller, J.P.; Iracane, D.; Lansiart, S.; Lemoine, P.; Lenain, R.; Marsault, Ph.; Michel, B.; Noirot, J.; Parrat, D.; Pelletier, M.; Perrais, Ch.; Phelip, M.; Pillon, S.; Poinssot, Ch.; Vallory, J.; Valot, C.; Pradel, Ph.; Bonin, B.; Bouquin, B.; Dozol, M.; Lecomte, M.; Vallee, A.; Bazile, F.; Parisot, J.F.; Finot, P.; Roberts, J.F

    2009-07-01

    Fuel is one of the essential components in a reactor. It is within that fuel that nuclear reactions take place, i.e. fission of heavy atoms, uranium and plutonium. Fuel is at the core of the reactor, but equally at the core of the nuclear system as a whole. Fuel design and properties influence reactor behavior, performance, and safety. Even though it only accounts for a small part of the cost per kilowatt-hour of power provided by current nuclear power plants, good utilization of fuel is a major economic issue. Major advances have yet to be achieved, to ensure longer in-reactor dwell-time, thus enabling fuel to yield more energy; and improve ruggedness. Aside from economics, and safety, such strategic issues as use of plutonium, conservation of resources, and nuclear waste management have to be addressed, and true technological challenges arise. This Monograph surveys current knowledge regarding in-reactor behavior, operating limits, and avenues for R and D. It also provides illustrations of ongoing research work, setting out a few noteworthy results recently achieved. Content: 1 - Introduction; 2 - Water reactor fuel: What are the features of water reactor fuel? 9 (What is the purpose of a nuclear fuel?, Ceramic fuel, Fuel rods, PWR fuel assemblies, BWR fuel assemblies); Fabrication of water reactor fuels (Fabrication of UO{sub 2} pellets, Fabrication of MOX (mixed uranium-plutonium oxide) pellets, Fabrication of claddings); In-reactor behavior of UO{sub 2} and MOX fuels (Irradiation conditions during nominal operation, Heat generation, and removal, The processes involved at the start of irradiation, Fission gas behavior, Microstructural changes); Water reactor fuel behavior in loss of tightness conditions (Cladding, the first containment barrier, Causes of failure, Consequences of a failure); Microscopic morphology of fuel ceramic and its evolution under irradiation; Migration and localization of fission products in UOX and MOX matrices (The ceramic under

  6. Surface Modification Reaction of Photocatalytic Titanium Dioxide with Triethoxysilane for Improving Dispersibility

    International Nuclear Information System (INIS)

    Lee, Myung Jin; Kim, Ji Ho; Park, Young Tae

    2010-01-01

    We have carried out the surface modification of photocatalytic TiO 2 with triethoxysilane through dehydrogenation reaction and characterized the modified photocatalyst by spectroscopic methods, such as FT-IR, solid-state 29 Si MAS NMR, XPS, and XRF, etc. We also examined photocatalytic activity of the immobilized photocatalytic titanium dioxide with triethoxysilane by decolorization reaction of dyes such as cong red and methylene blue under visible light. Dispersion test showed that the photocatalytic titanium dioxide immobilized with triethoxysilane group has kept higher dispersibility than titanium dioxide itself. No appreciable precipitation takes place even after standing for 24 h in the 4:6 mixture ratio of ethanol and water

  7. Fuel assembly

    International Nuclear Information System (INIS)

    Fujibayashi, Toru.

    1970-01-01

    Herein disclosed is a fuel assembly in which a fuel rod bundle is easily detachable by rotating a fuel rod fastener rotatably mounted to the upper surface of an upper tie-plate supporting a fuel bundle therebelow. A locking portion at the leading end of each fuel rod protrudes through the upper tie-plate and is engaged with or separated from the tie-plate by the rotation of the fastener. The removal of a desired fuel rod can therefore be remotely accomplished without the necessity of handling pawls, locking washers and nuts. (Owens, K.J.)

  8. Nuclear fuel

    International Nuclear Information System (INIS)

    D Hondt, P.

    1998-01-01

    The research and development programme on nuclear fuel at the Belgian Nuclear Research Centre SCK/CEN is described. The objective of this programme is to enhance the quantitative prediction of the operational limits of nuclear fuel and to assess the behaviour of fuel under incidental and accidental conditions. Progress is described in different domains including the modelling of fission gas release in LWR fuel, thermal conductivity, basic physical phenomena, post-irradiation examination for fuel performance assessment, and conceptual studies of incidental and accidental fuel experiments

  9. Fuel management

    International Nuclear Information System (INIS)

    Schwarz, E.R.

    1975-01-01

    Description of the operation of power plants and the respective procurement of fuel to fulfil the needs of the grid. The operation of the plants shall be optimised with respect to the fuel cost. (orig./RW) [de

  10. Fuel gases

    International Nuclear Information System (INIS)

    Anon.

    1996-01-01

    This paper gives a brief presentation of the context, perspectives of production, specificities, and the conditions required for the development of NGV (Natural Gas for Vehicle) and LPG-f (Liquefied Petroleum Gas fuel) alternative fuels. After an historical presentation of 80 years of LPG evolution in vehicle fuels, a first part describes the economical and environmental advantages of gaseous alternative fuels (cleaner combustion, longer engines life, reduced noise pollution, greater natural gas reserves, lower political-economical petroleum dependence..). The second part gives a comparative cost and environmental evaluation between the available alternative fuels: bio-fuels, electric power and fuel gases, taking into account the processes and constraints involved in the production of these fuels. (J.S.)

  11. Fuel cycles

    International Nuclear Information System (INIS)

    Hawley, N.J.

    1983-05-01

    AECL publications, from the open literature, on fuels and fuel cycles used in CANDU reactors are listed in this bibliography. The accompanying index is by subject. The bibliography will be brought up to date periodically

  12. Nuclear fuels

    International Nuclear Information System (INIS)

    2008-01-01

    The nuclear fuel is one of the key component of a nuclear reactor. Inside it, the fission reactions of heavy atoms, uranium and plutonium, take place. It is located in the core of the reactor, but also in the core of the whole nuclear system. Its design and properties influence the behaviour, the efficiency and the safety of the reactor. Even if it represents a weak share of the generated electricity cost, its proper use represents an important economic stake. Important improvements remain to be made to increase its residence time inside the reactor, to supply more energy, and to improve its robustness. Beyond the economical and safety considerations, strategical questions have to find an answer, like the use of plutonium, the management of resources and the management of nuclear wastes and real technological challenges have to be taken up. This monograph summarizes the existing knowledge about the nuclear fuel, its behaviour inside the reactor, its limits of use, and its R and D tracks. It illustrates also the researches in progress and presents some key results obtained recently. Content: 1 - Introduction; 2 - The fuel of water-cooled reactors: aspect, fabrication, behaviour of UO 2 and MOX fuels inside the reactor, behaviour in loss of tightness situation, microscopic morphology of fuel ceramics and evolution under irradiation - migration and localisation of fission products in UOX and MOX matrices, modeling of fuels behaviour - modeling of defects and fission products in the UO 2 ceramics by ab initio calculations, cladding and assembly materials, pellet-cladding interaction, advanced UO 2 and MOX ceramics, mechanical behaviour of the fuel assembly, fuel during a loss of coolant accident, fuel during a reactivity accident, fuel during a serious accident, fuel management inside reactor cores, fuel cycle materials balance, long-term behaviour of the spent fuel, fuel of boiling water reactors; 3 - the fuel of liquid metal fast reactors: fast neutrons radiation

  13. Fuel pellet

    International Nuclear Information System (INIS)

    Hayashi, K.

    1980-01-01

    Fuel pellet for insertion into a cladding tube in order to form a fuel element or a fuel rod. The fuel pellet has got a belt-like projection around its essentially cylindrical lateral circumferential surface. The upper and lower edges in vertical direction of this belt-like projection are wave-shaped. The projection is made of the same material as the bulk pellet. Both are made in one piece. (orig.) [de

  14. Fossil Fuels.

    Science.gov (United States)

    Crank, Ron

    This instructional unit is one of 10 developed by students on various energy-related areas that deals specifically with fossil fuels. Some topics covered are historic facts, development of fuels, history of oil production, current and future trends of the oil industry, refining fossil fuels, and environmental problems. Material in each unit may…

  15. Fuel element

    International Nuclear Information System (INIS)

    1974-01-01

    A new fuel can with a loose bottom and head is described. The fuel bar is attached to the loose bottom and head with two grid poles keeping the distance between bottom and head. A bow-shaped handle is attached to the head so that the fuel bar can be lifted from the can

  16. Real time, in situ observation of the photocatalytic inactivation of Saccharomyces cerevisiae cells

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jingtao [School of Food and Bioengineering, Zhengzhou University of Light Industry, Zhengzhou 450002 (China); Environment Functional Materials Division, Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016 (China); Wang, Xiaoxin [Environment Functional Materials Division, Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016 (China); Li, Qi, E-mail: qili@imr.ac.cn [Environment Functional Materials Division, Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016 (China); Shang, Jian Ku [Environment Functional Materials Division, Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016 (China); Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801 (United States)

    2015-04-01

    An in situ microscopy technique was developed to observe in real time the photocatalytic inactivation process of Saccharomyces cerevisiae (S. cerevisiae) cells by palladium-modified nitrogen-doped titanium oxide (TiON/PdO) under visible light illumination. The technique was based on building a photocatalytic micro-reactor on the sample stage of a fluorescence/phase contrast microscopy capable of simultaneously providing the optical excitation to activate the photocatalyst in the micro-reactor and the illumination to acquire phase contrast images of the cells undergoing the photocatalytic inactivation process. Using TiON/PdO as an example, the technique revealed for the first time the vacuolar activities inside S. cerevisiae cells subjected to a visible light photocatalytic inactivation. The vacuoles responded to the photocatalytic attack by the first expansion of the vacuolar volume and then contraction, before the vacuole disappeared and the cell structure collapsed. Consistent with the aggregate behavior observed from the cell culture experiments, the transition in the vacuolar volume provided clear evidence that photocatalytic disinfection of S. cerevisiae cells started with an initiation period in which cells struggled to offset the photocatalytic damage and moved rapidly after the photocatalytic damage overwhelmed the defense mechanisms of the cells against oxidative attack. - Highlights: • Palladium-modified nitrogen-doped titanium oxidephotocatalyst (TiON/PdO) • Effective visible-light photocatalytic disinfection of yeast cells by TiON/PdO • Real time, in situ observation technique was developed for photocatalytic disinfection. • The fluorescence/phase contrast microscope with a photocatalytic micro-reactor • Yeast cell disinfection happened before the cell structure collapsed.

  17. Photocatalytic Oxidation and Reduction Chemistry and a New Process for Treatment of Pink Water and Related Contaminated Water

    Science.gov (United States)

    1996-10-01

    Influence of pH on the Degradation Kinetics of Nitrophenol Isomers in a Heterogeneous ...34 Heterogeneous Photocatalytic Degradation of Organic Water Contaminants: Kinetics and Hydroxyl Radical Mechanisms," Ph.D. Thesis, Raleigh, NC: North Carolina...Dioxide Systems : Photocatalytic Degradation of Chloro- and Nitrophenols ." Trace Met. Environ 3, no. Photocatalytic Purification and Treatment of Water

  18. Cadmium Sulphide Nanorods: Synthesis, Characterization and their Photocatalytic Activity

    International Nuclear Information System (INIS)

    Giribabu, Krishnamoorthy; Suresh, Ranganathan; Manigandan, Ramadoss; Vijayaraj, Arunachalam; Prabu, Raju; Narayanan, Vengidusamy

    2012-01-01

    Cadmium sulphide (CdS) nanorods were prepared by a single precursor thermal decomposition (SPTD) method. The formation of CdS nanorods and their structure, morphology and elemental composition were studied by means of FT-IR, XRD, FE-SEM, HR-TEM and EDAX analysis. Photoluminescence (PL) and lifetime measurements were recorded to study the luminescence properties of the material. The PL spectrum of the CdS nanorods showed one broad peak and four shoulders and the cause for this emission was discussed. The PL emissions from the band edge and deep trap state of the CdS nanorods were studied by lifetime measurements. Further, the synthesized CdS nanorods showed an increase in efficiency of photocatalytic degradation of methylene blue (MB) and rhodamine B (RhB). The increase in the photocatalytic activity was attributed to the mixed phase of the CdS nanorods

  19. Cadmium Sulphide Nanorods: Synthesis, Characterization and their Photocatalytic Activity

    Energy Technology Data Exchange (ETDEWEB)

    Giribabu, Krishnamoorthy; Suresh, Ranganathan; Manigandan, Ramadoss; Vijayaraj, Arunachalam; Prabu, Raju; Narayanan, Vengidusamy [Univ. of Madras, Madras (India)

    2012-09-15

    Cadmium sulphide (CdS) nanorods were prepared by a single precursor thermal decomposition (SPTD) method. The formation of CdS nanorods and their structure, morphology and elemental composition were studied by means of FT-IR, XRD, FE-SEM, HR-TEM and EDAX analysis. Photoluminescence (PL) and lifetime measurements were recorded to study the luminescence properties of the material. The PL spectrum of the CdS nanorods showed one broad peak and four shoulders and the cause for this emission was discussed. The PL emissions from the band edge and deep trap state of the CdS nanorods were studied by lifetime measurements. Further, the synthesized CdS nanorods showed an increase in efficiency of photocatalytic degradation of methylene blue (MB) and rhodamine B (RhB). The increase in the photocatalytic activity was attributed to the mixed phase of the CdS nanorods.

  20. MWCNT/CdS hybrid nanocomposite for enhanced photocatalytic activity

    International Nuclear Information System (INIS)

    Chaudhary, Deepti; Khare, Neeraj; Vankar, V. D.

    2016-01-01

    Multi-walled carbon nanotubes (MWCNT)/CdS hybrid nanocomposite were synthesized by one step hydrothermal method. MWCNTs were used as a substrate for the growth of CdS nanoparticles. MWCNT/CdS nanocomposite and pure CdS were characterized by XRD, TEM, UV-vis and photoluminescence spectroscopy. HRTEM study confirms the intimate contact of CdS with MWCNT. The photocatalytic activity of nanocomposite was studied for the degradation of methylene blue dye under UV irradiation. The enhanced photocatalytic activity of MWCNT/CdS nanocomposite as compared to pure CdS has been attributed to reduced recombination of photogenerated charge carriers due to interfacial electron transfer from CdS to MWCNT.

  1. Transferring Knowledge of Electrocatalysis to Photocatalysis: Photocatalytic Water Splitting

    KAUST Repository

    Takanabe, Kazuhiro

    2017-06-24

    One of the most attractive features of photocatalytic reactions is the ability to achieve energetically uphill (photosynthetic) reactions. In many photocatalytic reactions, the reactions involve multielectron transfers with the adsorbed intermediates. In this case, photocatalysis is nothing but electrocatalysis initiated and driven by the electron potential shift caused by the photocatalyst (photon absorber). This condition is indeed true for photocatalysts for water splitting, which are also electrocatalysts because both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) require multiple electron transfers at the active surfaces. This chapter deals with the product-side in the six-gear concept. It shows the electrocatalytic performance when using an electrocatalyst on the surface. The chapter further shows the current-potential curve for an electrocatalytic process isolated from the photocatalyst process. For an electrocatalyst to achieve electrochemical reactions, the potential of the catalyst must be shifted at the interface of the semiconductor, providing electromotive force or overpotential for redox reactions.

  2. Transferring Knowledge of Electrocatalysis to Photocatalysis: Photocatalytic Water Splitting

    KAUST Repository

    Takanabe, Kazuhiro

    2017-01-01

    One of the most attractive features of photocatalytic reactions is the ability to achieve energetically uphill (photosynthetic) reactions. In many photocatalytic reactions, the reactions involve multielectron transfers with the adsorbed intermediates. In this case, photocatalysis is nothing but electrocatalysis initiated and driven by the electron potential shift caused by the photocatalyst (photon absorber). This condition is indeed true for photocatalysts for water splitting, which are also electrocatalysts because both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) require multiple electron transfers at the active surfaces. This chapter deals with the product-side in the six-gear concept. It shows the electrocatalytic performance when using an electrocatalyst on the surface. The chapter further shows the current-potential curve for an electrocatalytic process isolated from the photocatalyst process. For an electrocatalyst to achieve electrochemical reactions, the potential of the catalyst must be shifted at the interface of the semiconductor, providing electromotive force or overpotential for redox reactions.

  3. Recent Photocatalytic Applications for Air Purification in Belgium

    Directory of Open Access Journals (Sweden)

    Elia Boonen

    2014-07-01

    Full Text Available Photocatalytic concrete constitutes a promising technique to reduce a number of air contaminants such as NOx and VOC’s, especially at sites with a high level of pollution: highly trafficked canyon streets, road tunnels, the urban environment, etc. Ideally, the photocatalyst, titanium dioxide, is introduced in the top layer of the concrete pavement for best results. In addition, the combination of TiO2 with cement-based products offers some synergistic advantages, as the reaction products can be adsorbed at the surface and subsequently be washed away by rain. A first application has been studied by the Belgian Road Research Center (BRRC on the side roads of a main entrance axis in Antwerp with the installation of 10.000 m² of photocatalytic concrete paving blocks. For now however, the translation of laboratory testing towards results in situ remains critical of demonstrating the effectiveness in large scale applications. Moreover, the durability of the air cleaning characteristic with time remains challenging for application in concrete roads. From this perspective, several new trial applications have been initiated in Belgium in recent years to assess the “real life” behavior, including a field site set up in the Leopold II tunnel of Brussels and the construction of new photocatalytic pavements on industrial zones in the cities of Wijnegem and Lier (province of Antwerp. This paper first gives a short overview of the photocatalytic principle applied in concrete, to continue with some main results of the laboratory research recognizing the important parameters that come into play. In addition, some of the methods and results, obtained for the existing application in Antwerp (2005 and during the implementation of the new realizations in Wijnegem and Lier (2010–2012 and in Brussels (2011–2013, will be presented.

  4. Photocatalytic Water Treatment on TiO2 Thin Layers.

    Czech Academy of Sciences Publication Activity Database

    Šolcová, Olga; Spáčilová, L.; Maléterová, Ywetta; Morozová, Magdalena; Ezechiáš, Martin; Křesinová, Zdena

    2016-01-01

    Roč. 57, č. 25 (2016), s. 11631-11638 ISSN 1944-3994. [International Conference on Protection and Restoration of the Environment /12./. Skiathos Island, 29.06.2014-03.07.2014] R&D Projects: GA TA ČR TA01020804 Institutional support: RVO:67985858 ; RVO:61388971 Keywords : water purification * endocrine disruptor * photocatalytic * TiO2 layers Subject RIV: CI - Industrial Chemistry, Chemical Engineering; EE - Microbiology, Virology (MBU-M) Impact factor: 1.631, year: 2016

  5. Preparation, characterization and photocatalytic studies of Cu , Sn ...

    Indian Academy of Sciences (India)

    method. Metal ions (Cu2+ and Sn2+), and non-metal anion, N3−, were substituted into the K5Sb5P2O20 for pos- ... in the photocatalytic reaction was studied using their appropriate scavengers. Keywords. ... K5Sb5P2O20 and exchange of its potassium with copper and tin ions ... distilled water and dried in air at 100. ◦. C.

  6. LPG fuel

    International Nuclear Information System (INIS)

    Dagnas, F.X.; Jeuland, N.; Fouquet, J.P.; Lauraire, S.; Coroller, P.

    2005-01-01

    LPG fuel has become frequently used through a distribution network with 2 000 service stations over the French territory. LPG fuel ranks number 3 world-wide given that it can be used on individual vehicles, professional fleets, or public transport. What is the environmental benefit of LPG fuel? What is the technology used for these engines? What is the current regulation? Government commitment and dedication on support to promote LPG fuel? Car makers projects? Actions to favour the use of LPG fuel? This article gathers 5 presentations about this topic given at the gas conference

  7. Photocatalytic degradation of rosuvastatin: Analytical studies and toxicity evaluations

    Energy Technology Data Exchange (ETDEWEB)

    Machado, Tiele Caprioli, E-mail: tiele@enq.ufrgs.br [Chemical Engineering Department, Federal University of Rio Grande do Sul, Rua Engenheiro Luiz Englert s/n, CEP: 90040-040 Porto Alegre, RS (Brazil); Pizzolato, Tânia Mara [Chemical Institute, Federal University of Rio Grande do Sul, Avenida Bento Gonçalves, 9500, CEP: 91501-970 Porto Alegre, RS (Brazil); Arenzon, Alexandre [Ecology Center, Federal University of Rio Grande do Sul, Avenida Bento Gonçalves, 9500, CEP: 91501-970 Porto Alegre, RS (Brazil); Segalin, Jeferson [Biotechnology Center, Federal University of Rio Grande do Sul, Avenida Bento Gonçalves, 9500, CEP: 91501-970 Porto Alegre, RS (Brazil); Lansarin, Marla Azário [Chemical Engineering Department, Federal University of Rio Grande do Sul, Rua Engenheiro Luiz Englert s/n, CEP: 90040-040 Porto Alegre, RS (Brazil)

    2015-01-01

    Photocatalytic degradation of rosuvastatin, which is a drug that has been used to reduce blood cholesterol levels, was studied in this work employing ZnO as catalyst. The experiments were carried out in a temperature-controlled batch reactor that was irradiated with UV light. Preliminary the effects of the photocatalyst loading, the initial pH and the initial rosuvastatin concentration were evaluated. The experimental results showed that rosuvastatin degradation is primarily a photocatalytic process, with pseudo-first order kinetics. The byproducts that were generated during the oxidative process were identified using nano-ultra performance liquid chromatography tandem mass spectrometry (nano-UPLC–MS/MS) and acute toxicity tests using Daphnia magna were done to evaluate the toxicity of the untreated rosuvastatin solution and the reactor effluent. - Highlights: • The photocatalytic degradation of rosuvastatin was studied under UV irradiation. • Commercial catalyst ZnO was used. • Initial rosuvastatin concentration, photocatalyst loading and pH were evaluated. • The byproducts generated during the oxidative process were detected and identified. • Acute toxicity tests using Daphnia magna were carried out.

  8. Advances in Photocatalytic CO2 Reduction with Water: A Review

    Directory of Open Access Journals (Sweden)

    Samsun Nahar

    2017-06-01

    Full Text Available In recent years, the increasing level of CO2 in the atmosphere has not only contributed to global warming but has also triggered considerable interest in photocatalytic reduction of CO2. The reduction of CO2 with H2O using sunlight is an innovative way to solve the current growing environmental challenges. This paper reviews the basic principles of photocatalysis and photocatalytic CO2 reduction, discusses the measures of the photocatalytic efficiency and summarizes current advances in the exploration of this technology using different types of semiconductor photocatalysts, such as TiO2 and modified TiO2, layered-perovskite Ag/ALa4Ti4O15 (A = Ca, Ba, Sr, ferroelectric LiNbO3, and plasmonic photocatalysts. Visible light harvesting, novel plasmonic photocatalysts offer potential solutions for some of the main drawbacks in this reduction process. Effective plasmonic photocatalysts that have shown reduction activities towards CO2 with H2O are highlighted here. Although this technology is still at an embryonic stage, further studies with standard theoretical and comprehensive format are suggested to develop photocatalysts with high production rates and selectivity. Based on the collected results, the immense prospects and opportunities that exist in this technique are also reviewed here.

  9. Doped titanium dioxide nanocrystalline powders with high photocatalytic activity

    International Nuclear Information System (INIS)

    Castro, A.L.; Nunes, M.R.; Carvalho, M.D.; Ferreira, L.P.; Jumas, J.-C.; Costa, F.M.; Florencio, M.H.

    2009-01-01

    Doped titanium dioxide nanopowders (M:TiO 2 ; M=Fe, Co, Nb, Sb) with anatase structure were successfully synthesized through an hydrothermal route preceded by a precipitation doping step. Structural and morphological characterizations were performed by powder XRD and TEM. Thermodynamic stability studies allowed to conclude that the anatase structure is highly stable for all doped TiO 2 prepared compounds. The photocatalytic efficiency of the synthesized nanopowders was tested and the results showed an appreciable enhancement in the photoactivity of the Sb:TiO 2 and Nb:TiO 2 , whereas no photocatalytic activity was detected for the Fe:TiO 2 and Co:TiO 2 nanopowders. These results were correlated to the doping ions oxidation states, determined by Moessbauer spectroscopy and magnetization data. - Graphical abstract: Doped titanium dioxide nanopowders (M:TiO 2 ; M=Fe, Co, Nb, Sb) with highly stable anatase structure were successfully synthesized through an hydrothermal route. The photocatalytic efficiencies of the synthesized nanopowders were tested and the results show an appreciable enhancement in the photoactivity of the Sb:TiO 2 and Nb:TiO 2 .

  10. Solution-derived photocatalytic films for environmental cleaning applications

    International Nuclear Information System (INIS)

    Štangar, U Lavrencic; Kete, M; Šuligoj, A; Tasbihi, M

    2012-01-01

    When photocatalytic water treatment is concerned, suspended catalyst in the aqueous phase is usually more efficient than immobilized on an inert support, but in the former case an undesirable separation/recycling step is needed. We have therefore concentrated on the preparation of immobilized catalysts in the form of films on glass and aluminium supports. The low-temperature sol-gel processing route to obtain transparent thin TiO 2 /SiO 2 films for self-cleaning purposes and thicker TiO 2 /SiO 2 coatings for efficient removal of pollutants in water and air are presented. The synthesis is based on a production of a nanocrystalline titania sol with a silica binder that after deposition does not require thermal treatment at high temperatures. Depending on the target application, some specific synthesis parameters and photocatalytic activity testing conditions are illustrated. For water-cleaning coatings fast kinetics is required, which was achieved by addition of a highly active titania powder into the sol. The same preparation procedure was used to prepare efficient air-cleaning coatings. On the other hand, self-cleaning films were thinner and transparent to keep the original appearance of the substrate and they solidified at ambient conditions. Advanced methodologies to evaluate photocatalytic activity of the films were applied.

  11. Photocatalytic efficiency of titania photocatalysts in saline waters

    Directory of Open Access Journals (Sweden)

    Albrbar Asma Juma

    2014-01-01

    Full Text Available The photocatalytic efficiency of the recently synthesized TiO2 powder, named P160, of the degradation of dye Dye C.I. Reactive orange 16 in natural and artificial seawater was investigated in comparison to its efficiency in deionized water and the efficiency of a standard TiO2 powder Degusa P25. It was shown that the photocatalytic efficiency of P160 was slightly higher than that of P25, probably due to slightly higher specific surface area, higher pore volume and larger pores of the powder P160. The efficiency of both photocatalysts in natural and artificial seawater was significantly lower than that in deionized water. The overall rate of dye degradation for both types of photocatalysts is litle higher in artificial seawater than in natural seawater, which shows the influence of organic compounds naturally present in seawater on the photocatalysts activity. A saturation Langmuir-type relationship between the initial degradation rate and the initial dye concentration indicates that the adsorption plays a role in the photocatalytic reaction. The photodegradation rate constant k, which represents the maximum reaction rate, has similar values for P25 and P160 in all types of water due to the similar properties of the photocatalysts. [Projekat Ministarstva nauke Republike Srbije, br III 45019

  12. Photocatalytic Nanocomposites for the Protection of European Architectural Heritage.

    Science.gov (United States)

    Gherardi, Francesca; Roveri, Marco; Goidanich, Sara; Toniolo, Lucia

    2018-01-03

    In the field of stone protection, the introduction of inorganic nanoparticles, such as TiO₂, ZnO, and Ag in polymeric blends can enhance the protective action of pristine treatments, as well as confer additional properties (photocatalytic, antifouling, and antibacterial). In the framework of the "Nano-Cathedral" European project, nanostructured photocatalytic protective treatments were formulated by using different TiO₂ nanoparticles, solvents, and silane/siloxane systems in the blends. The results about the characterization and application of two promising nano-TiO₂ based products applied on Apuan marble and Ajarte limestone are here reported, aiming at investigating the complex system "treatment/stone-substrate". The nanocomposites show better performances when compared to a commercial reference siloxane based protective treatment, resulting in different performances once applied on different carbonatic substrates, with very low and high open porosity, confirming the necessity of correlating precisely the characteristics of the stone material to those of the protective formulations. In particular, the TiO₂ photocatalytic behavior is strictly linked to the amount of available nanoparticles and to the active surface area. The alkyl silane oligomers of the water-based formulation have a good penetration into the microstructure of Ajarte limestone, whereas the solvent-based and small size monomeric formulation shows better results for Apuan marble, granting a good coverage of the pores. The encouraging results obtained so far in lab will be confirmed by monitoring tests aiming at assessing the effectiveness of the treatments applied in pilot sites of historical Gothic Cathedrals.

  13. Photocatalytic degradation of methyl red dye by silica nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Badr, Y. [National Institute of Laser Enhanced Science, Cairo University, Cairo (Egypt); Abd El-Wahed, M.G. [Chemistry Department, Faculty of Science, Zagazig University, Zagazig (Egypt); Mahmoud, M.A. [Chemistry Department, Faculty of Science, Zagazig University, Zagazig (Egypt)], E-mail: mahmoudchem@yahoo.com

    2008-06-15

    Silica nanoparticles (SiO{sub 2} NPs) were found to be photocatalytically active for degradation of methyl red dye (MR). The SiO{sub 2} NPs and SiO{sub 2} NPs doped with silver (and or) gold nanoparticles were prepared. From the transmission electron microscopy (TEM) images the particle size and particle morphology of catalysts were monitored. Moreover, SiO{sub 2} NPs doped with silver and gold ions were used as a photocatalyst for degradation of MR. The rate of photocatalytic degradation of MR was found to be increased in the order of SiO{sub 2} NPs, SiO{sub 2} NPs coated with gold nanoparticles (Au NPs) and silver nanoparticles (Ag NPs), SiO{sub 2} NPs coated with Ag NPs, SiO{sub 2} NPs coated with Au NPs, Ag{sup +}-doped SiO{sub 2} NPs, and Au{sup 3+}-doped SiO{sub 2} NPs. The kinetic and mechanism of photocatalytic reaction were studied and accorded well with experimental results.

  14. Photocatalytic Performance of Carbon Monolith/TiO2 Composite

    Directory of Open Access Journals (Sweden)

    Marina Maletić

    2015-01-01

    Full Text Available The new and simple approach for deposition of catalytically active TiO2 coating on carbon monolith (CM carrier was presented. CM photocatalysts were impregnated with TiO2 using titanium solution and thermal treatment, and their photocatalytic activity was investigated in the process of methylene blue (MB photodegradation. For the purpose of comparison, CM composite photocatalysts were prepared by dip-coating method, which implies binder usage. The presence of TiO2 on CM carrier was confirmed by Raman spectroscopy and scanning electron microscopy. The sorption characteristics of CM and the role of adsorption in the overall process of MB removal were evaluated through amount of surface oxygen groups obtained by temperature-programmed desorption and specific surface area determined by BET method. CM has shown good adsorption properties toward MB due to high amount of surface oxygen groups and relatively high specific surface area. It was concluded that photocatalytic activity increases with CM disc thickness due to increase of MB adsorption and amount of deposited TiO2. Good photocatalytic activity achieved for samples obtained by thermal treatment is the result of better accessibility of MB solution to the TiO2 particles induced by binder absence.

  15. Applied studies in solar photocatalytic detoxification: an overview

    Energy Technology Data Exchange (ETDEWEB)

    Malato, S.; Blanco, J.; Vidal, A.; Alarcon, D.; Maldonado, M.I.; Caceres, J.; Gernjak, W. [CIEMAT - Plataforma Solar de Almeria, Tabernas (Spain)

    2003-10-01

    The technical feasibility and performance of photocatalytic degradation of four water-soluble pesticides (diuron, imidacloprid, formetanate and methomyl) have been studied at pilot scale in two well-defined systems which are of special interest because natural-solar UV light can be used for them: heterogeneous photocatalysis with titanium dioxide and homogeneous photocatalysis by photo-Fenton. The pilot plant is made up of compound parabolic collectors specially designed for solar photocatalytic applications. The initial concentration tested with imidacloprid, formetanate and methomyl was 50 and 30 mg/l with diuron, and the catalyst concentrations were 200 mg/l and 0.05 mM with TiO{sub 2} and iron, respectively. Total disappearance of the parent compounds, 90% mineralisation and toxicity reduction below the threshold (EC{sub 50}) have been attained with all pesticides tested. All these results have contributed to an evaluation of photocatalytic treatment capacity and comments on the main parameters of TiO{sub 2} and Fe separation from the treated water. (author)

  16. Bismuth titanate nanorods and their visible light photocatalytic properties

    International Nuclear Information System (INIS)

    Pei, L.Z.; Liu, H.D.; Lin, N.; Yu, H.Y.

    2015-01-01

    Highlights: • Bismuth titanate nanorods have been synthesized by a simple hydrothermal process. • The size of bismuth titanate nanorods can be controlled by growth conditions. • Bismuth titanate nanorods show good photocatalytic activities of methylene blue and Rhodamine B. - Abstract: Bismuth titanate nanorods have been prepared using a facile hydrothermal process without additives. The bismuth titanate products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM) and UV-vis diffusion reflectance spectrum. XRD pattern shows that the bismuth titanate nanorods are composed of cubic Bi 2 Ti 2 O 7 phase. Electron microscopy images show that the length and diameter of the bismuth titanate nanorods are 50-200 nm and 2 μm, respectively. Hydrothermal temperature and reaction time play important roles on the formation and size of the bismuth titanate nanorods. UV-vis diffusion reflectance spectrum indicates that bismuth titanate nanorods have a band gap of 2.58 eV. The bismuth titanate nanorods exhibit good photocatalytic activities in the photocatalytic degradation of methylene blue (MB) and Rhodamine B (RB) under visible light irradiation. The bismuth titanate nanorods with cubic Bi 2 Ti 2 O 7 phase are a promising candidate as a visible light photocatalyst

  17. Photocatalytic hydrogen evolution from aqueous solutions of organophosphorous compounds

    Energy Technology Data Exchange (ETDEWEB)

    Kozlova, Ekaterina A.; Vorontsov, Alexander V. [Boreskov Institute of Catalysis and Novosibirsk State University, Novosibirsk 630090 (Russian Federation)

    2010-07-15

    Photocatalytic hydrogen production from water solutions of dimethyl methylphosphonate (DMMP), trimethyl phosphate (TMP), triethyl phosphate (TEP), and radiation protective amine WR 2721, that imitate nerve chemical warfare agents was studied for the first time. Platinized titianium dioxide Degussa P25 was used as catalyst. No significant hydrogen evolution was detected without organic electron donors - sacrificial agents. The hydrogen evolution rate was shown to grow slowly with the rise of initial DMMP concentration. The initial rate vs. DMMP concentration curve is well fitted by Langmuir-Hinshelwood (L-H) equation. The DMMP adsorption constant obtained from the L-H equation fit is markedly higher than that obtained from the Langmuir adsorption isotherm. Reactions of full destruction into inorganic products of the four organophosphorous compounds were conducted. Amounts of evolved hydrogen and carbon dioxide were completely consistent with stoichiometry of proposed reaction. There were no initial compounds and only trace of total organic carbon after the end of the reaction. Complete water purification and production of an amount of valuable hydrogen was achieved. Intermediates of DMMP oxygen-free destruction were identified by means of GC/MS. They were the same as those in the case of DMMP photocatalytic oxidation. A mechanism of hydrogen evolution that explains smaller rates of mineralization compared to photocatalytic oxidation by oxygen was proposed. (author)

  18. Nitrogen-Doped Graphene for Photocatalytic Hydrogen Generation.

    Science.gov (United States)

    Chang, Dong Wook; Baek, Jong-Beom

    2016-04-20

    Photocatalytic hydrogen (H2 ) generation in a water splitting process has recently attracted tremendous interest because it allows the direct conversion of clean and unlimited solar energy into the ideal energy resource of H2 . For efficient photocatalytic H2 generation, the role of the photocatalyst is critical. With increasing demand for more efficient, sustainable, and cost-effective photocatalysts, various types of semiconductor photocatalysts have been intensively developed. In particular, on the basis of its superior catalytic and tunable electronic properties, nitrogen-doped graphene is a potential candidate for a high-performance photocatalyst. Nitrogen-doped graphene also offers additional advantages originating from its unique two-dimensional sp(2) -hybridized carbon network including a large specific surface area and exceptional charge transport properties. It has been reported that nitrogen-doped graphene can play diverse but positive functions including photo-induced charge acceptor/meditator, light absorber from UV to visible light, n-type semiconductor, and giant molecular photocatalyst. Herein, we summarize the recent progress and general aspects of nitrogen-doped graphene as a photocatalyst for photocatalytic H2 generation. In addition, challenges and future perspectives in this field are also discussed. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Fuel assembly

    International Nuclear Information System (INIS)

    Ueda, Makoto; Ogiya, Shunsuke.

    1989-01-01

    For improving the economy of a BWR type reactor by making the operation cycle longer, the fuel enrichment degree has to be increased further. However, this makes the subcriticality shallower in the upper portion of the reactor core, to bring about a possibility that the reactor shutdown becomes impossible. In the present invention, a portion of fuel rod is constituted as partial length fuel rods (P-fuel rods) in which the entire stack length in the effective portion is made shorter by reducing the concentration of fissionable materials in the axial portion. A plurality of moderator rods are disposed at least on one diagonal line of a fuel assembly and P-fuel rods are arranged at a position put between the moderator rods. This makes it possible to reactor shutdown and makes the axial power distribution satisfactory even if the fuel enrichment degree is increased. (T.M.)

  20. Fuel Services

    International Nuclear Information System (INIS)

    Silberstein, A.

    1982-09-01

    FRAGEMA has developed most types of inspection equipments to work on irradiated fuel assemblies and on single fuel rods during reactor outages with an efficiency compatible with the utilities operating priorities. In order to illustrate this statement, two specific examples of inspection equipments are shortly described: the on-site removable fuel rod assembly examination stand, and the fuel assembly multiple examination device. FRAGEMA has developed techniques for the identifiction of the leaking fuel rods in the fuel assembly and the tooling necessary to perform the replacement of the faulted element. These examples of methods, techniques and equipments described and the experience accumulated through their use allow FRAGEMA to qualify for offering the supply of the corresponding software, hardware or both whenever an accurate understanding of the fuel behaviour is necessary and whenever direct intervention on the assembly and associated components is necessary due to safety, operating or economical reasons

  1. Fuel assembly

    International Nuclear Information System (INIS)

    Watanabe, Shoichi; Hirano, Yasushi.

    1998-01-01

    A one-half or more of entire fuel rods in a fuel assembly comprises MOX fuel rods containing less than 1wt% of burnable poisons, and at least a portion of the burnable poisons comprises gadolinium. Then, surplus reactivity at an initial stage of operation cycle is controlled to eliminate burnable poisons remained unburnt at a final stage, as well as increase thermal reactivity. In addition, the content of fission plutonium is determined to greater than the content of uranium 235, and fuel rods at corner portions are made not to incorporate burnable poisons. Fuel rods not containing burnable poisons are disposed at positions in adjacent with fuel rods facing to a water rod at one or two directions. Local power at radial center of the fuel assembly is increased to flatten the distortion of radial power distribution. (N.H.)

  2. How Pt nanoparticles affect TiO2-induced gas-phase photocatalytic oxidation reactions

    NARCIS (Netherlands)

    Fraters, B.D.; Amrollahi Buky, Rezvaneh; Mul, Guido

    2015-01-01

    The effect of Pt nanoparticles on the gas-phase photocatalytic oxidation activity of TiO2 is shown to be largely dependent on the molecular functionality of the substrate. We demonstrate that Pt nanoparticles decrease rates in photocatalytic oxidation of propane, whereas a strong beneficial effect

  3. Photocatalytic oxidation of a reactive azo dye and evaluation of the ...

    African Journals Online (AJOL)

    The purpose of this study was to investigate the photocatalytic oxidation of a reactive azo dye and determine the improvement in the biodegradability when photocatalytic oxidation was used as a pretreatment step prior to biological treatment. The results obtained from the experiments adding H2O2/TiO2 show that the ...

  4. Synthesis, structure and photocatalytic activity of nano TiO2 and ...

    Indian Academy of Sciences (India)

    The material shows higher photocatalytic activity both in UV and visible region of the solar radiation compared to commercial Degussa P25 TiO2. Transition metal ion substitution for Ti4+ creates mid-gap states which act as recombination centers for electron{hole induced by photons thus reducing photocatalytic activity.

  5. Comparing the photocatalytic activity of TiO2 at macro- and microscopic scales

    DEFF Research Database (Denmark)

    Torras-Rosell, Antoni; Johannsen, Sabrina Rostgaard; Dirscherl, Kai

    2016-01-01

    . The photocatalytic properties of TiO2 at macro- and microscopic scales are investigated by comparing photocatalytic degradation of acetone and electrochemical experiments to Kelvin probe force microscopy. The good agreement between the macro- and microscopic experiments suggests that Kelvin probe force microscopy...

  6. Photocatalytic degradation of methylene blue by C 3 N 4 /ZnO

    Indian Academy of Sciences (India)

    The photocatalytic activities of prepared samples were investigated under the illumination of blacklight and fluorescent lamps as the low wattage light source. The C 3 N 4 /ZnO showed a better photocatalytic activity than ZnO to degrade a methylene blue (MB) dye solution using blacklight lamps, but there is no significant ...

  7. Photocatalytic reduction of CO2 to CO over copper decorated g-C3N4 nanosheets with enhanced yield and selectivity

    Science.gov (United States)

    Shi, Guodong; Yang, Lin; Liu, Zhuowen; Chen, Xiao; Zhou, Jianqing; Yu, Ying

    2018-01-01

    Photocatalytic reduction of CO2 to fuel has attracted considerable attention due to the consumption of fossil fuels and serious environmental problems. Although there are many photocatalysts reported for CO2 reduction, the improvement of activity and selectivity is still in great need of. In this work, a series of Cu nanoparticle decorated g-C3N4 nanosheets with different Cu loadings were fabricated by a facile secondary calcination and subsequent microwave hydrothermal method. The designed catalysts shown good photocatalytic activity and selectivity for CO2 reduction to CO. The optimal sample exhibited a 3-fold augmentation of the CO yield in comparison with pristine g-C3N4 under visible light. It is revealed that with the loading of Cu nanoparticles, the resulting photocatalyst possessed an improved charge carrier transfer and separation efficiency as well as increased surface reactive sites, resulting in a significant enhancement of CO yield. It is anticipated that the designed Cu/C3N4 photocatalyst may provide new insights for two dimensional layer materials and non-noble particles applied to CO2 reduction.

  8. Enhancement of photocatalytic property on ZnS/MoS2 composite under visible light irradiation

    Directory of Open Access Journals (Sweden)

    Cheng Jiushan

    2017-01-01

    Full Text Available In this paper, the composite ZnS/MoS2 was obtained via two steps including solvothermal methods. The as-synthesized sample was characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM and UV-Vis. diffuse reflectance spectra (DRS. The photocatalytic activity of the product was evaluated through photocatalytic degradation of Rhodamine B (Rh B under UV-Vis. light irradiation; the electrical conductivity of ZnS/MoS2 composites was significantly improved compared to ZnS, MoS2, respectively. The results showed that the ZnS/MoS2 composite photocatalyst possesses better photocatalytic activity in degrading Rh B than the single ZnS or the single MoS2. The better photocatalytic properties may be due to the synergetic effect of two semiconductors, because of which electrons and holes were separated effectively. And its specific microstructure played an active role in evaluating photocatalytic performance.

  9. Photocatalytic Reduction of Hexavalent Chromium Induced by Photolysis of Ferric/tartrate Complex

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Xianghua; Ding, Shimin; Zhang, Lixian [Yangtze Normal Univ., Fuling (China)

    2012-11-15

    Photocatalytic reduction of hexavalent chromium (Cr(VI)) in ferric-tartrate system under irradiation of visible light was investigated. Effects of light resources, initial pH value and initial concentration of various reactants on Cr(VI) photocatalytic reduction were studied. Photoreaction kinetics was discussed and a possible photochemical pathway was proposed. The results indicate that Fe(III)-tartrate system is able to rapidly and effectively photocatalytically reduce Cr(VI) utilizing visible light. Initial pH variations results in the concentration changes of Fe(III)-tartrate complex in this system, and pH at 3.0 is optimal for Cr(VI) photocatalytic reduction. Efficiency of Cr(VI) photocatalytic reduction increases with increasing initial concentrations of Cr(VI), Fe(III) and tartrate. Kinetics analysis indicates that initial Fe(III) concentration affects Cr(VI) photoreduction most significantly.

  10. Photocatalytic Reduction of Hexavalent Chromium Induced by Photolysis of Ferric/tartrate Complex

    International Nuclear Information System (INIS)

    Feng, Xianghua; Ding, Shimin; Zhang, Lixian

    2012-01-01

    Photocatalytic reduction of hexavalent chromium (Cr(VI)) in ferric-tartrate system under irradiation of visible light was investigated. Effects of light resources, initial pH value and initial concentration of various reactants on Cr(VI) photocatalytic reduction were studied. Photoreaction kinetics was discussed and a possible photochemical pathway was proposed. The results indicate that Fe(III)-tartrate system is able to rapidly and effectively photocatalytically reduce Cr(VI) utilizing visible light. Initial pH variations results in the concentration changes of Fe(III)-tartrate complex in this system, and pH at 3.0 is optimal for Cr(VI) photocatalytic reduction. Efficiency of Cr(VI) photocatalytic reduction increases with increasing initial concentrations of Cr(VI), Fe(III) and tartrate. Kinetics analysis indicates that initial Fe(III) concentration affects Cr(VI) photoreduction most significantly

  11. Charge Transfer Mechanism in Titanium-Doped Microporous Silica for Photocatalytic Water-Splitting Applications

    Directory of Open Access Journals (Sweden)

    Wendi Sapp

    2016-02-01

    Full Text Available Solar energy conversion into chemical form is possible using artificial means. One example of a highly-efficient fuel is solar energy used to split water into oxygen and hydrogen. Efficient photocatalytic water-splitting remains an open challenge for researchers across the globe. Despite significant progress, several aspects of the reaction, including the charge transfer mechanism, are not fully clear. Density functional theory combined with density matrix equations of motion were used to identify and characterize the charge transfer mechanism involved in the dissociation of water. A simulated porous silica substrate, using periodic boundary conditions, with Ti4+ ions embedded on the inner pore wall was found to contain electron and hole trap states that could facilitate a chemical reaction. A trap state was located within the silica substrate that lengthened relaxation time, which may favor a chemical reaction. A chemical reaction would have to occur within the window of photoexcitation; therefore, the existence of a trapping state may encourage a chemical reaction. This provides evidence that the silica substrate plays an integral part in the electron/hole dynamics of the system, leading to the conclusion that both components (photoactive materials and support of heterogeneous catalytic systems are important in optimization of catalytic efficiency.

  12. Fuel assembly

    International Nuclear Information System (INIS)

    Nakatsuka, Masafumi; Matsuzuka, Ryuji.

    1976-01-01

    Object: To provide a fuel assembly which can decrease pressure loss of coolant to uniform temperature. Structure: A sectional area of a flow passage in the vicinity of an inner peripheral surface of a wrapper tube is limited over the entire length to prevent the temperature of a fuel element in the outermost peripheral portion from being excessively decreased to thereby flatten temperature distribution. To this end, a plurality of pincture-frame-like sheet metals constituting a spacer for supporting a fuel assembly, which has a plurality of fuel elements planted lengthwise and in given spaced relation within the wrapper tube, is disposed in longitudinal grooves and in stacked fashion to form a substantially honeycomb-like space in cross section. The fuel elements are inserted and supported in the space to form a fuel assembly. (Kamimura, M.)

  13. Fuel assemblies

    International Nuclear Information System (INIS)

    Nagano, Mamoru; Yoshioka, Ritsuo

    1983-01-01

    Purpose: To effectively utilize nuclear fuels by increasing the reactivity of a fuel assembly and reduce the concentration at the central region thereof upon completion of the burning. Constitution: A fuel assembly is bisected into a central region and a peripheral region by disposing an inner channel box within a channel box. The flow rate of coolants passing through the central region is made greater than that in the peripheral region. The concentration of uranium 235 of the fuel rods in the central region is made higher. In such a structure, since the moderating effect in the central region is improved, the reactivity of the fuel assembly is increased and the uranium concentration in the central region upon completion of the burning can be reduced, fuel economy and effective utilization of uranium can be attained. (Kamimura, M.)

  14. Fuel assembly

    International Nuclear Information System (INIS)

    Bando, Masaru.

    1993-01-01

    As neutron irradiation progresses on a fuel assembly of an FBR type reactor, a strong force is exerted to cause ruptures if the arrangement of fuel elements is not displaced, whereas the fuel elements may be brought into direct contact with each other not by way of spacers to cause burning damages if the arrangement is displaced. In the present invention, the circumference of fuel elements arranged in a normal triangle lattice is surrounded by a wrapper tube having a hexagonal cross section, wire spacers are wound therearound, and deformable spacers are distributed to optional positions for fuel elements in the wrapper tube. Interaction between the fuel elements caused by irradiation is effectively absorbed, thereby enabling to delay the occurrence of the rupture and burning damages of the elements. (N.H.)

  15. Fuel assembly

    International Nuclear Information System (INIS)

    Yokota, Tokunobu.

    1990-01-01

    A fuel assembly used in a FBR type nuclear reactor comprises a plurality of fuel rods and a moderator guide member (water rod). A moderator exit opening/closing mechanism is formed at the upper portion of the moderator guide member for opening and closing a moderator exit. In the initial fuel charging operation cycle to the reactor, the moderator exit is closed by the moderator exit opening/closing mechanism. Then, voids are accumulated at the inner upper portion of the moderator guide member to harden spectrum and a great amount of plutonium is generated and accumulated in the fuel assembly. Further, in the fuel re-charging operation cycle, the moderator guide member is used having the moderator exit opened. In this case, voids are discharged from the moderator guide member to decrease the ratio, and the plutonium accumulated in the initial charging operation cycle is burnt. In this way, the fuel economy can be improved. (I.N.)

  16. Fuel spacer

    International Nuclear Information System (INIS)

    Nishida, Koji; Yokomizo, Osamu; Kanazawa, Toru; Kashiwai, Shin-ichi; Orii, Akihito.

    1992-01-01

    The present invention concerns a fuel spacer for a fuel assembly of a BWR type reactor and a PTR type reactor. Springs each having a vane are disposed on the side surface of a circular cell which supports a fuel rods. A vortex streams having a vertical component are formed by the vanes in the flowing direction of a flowing channel between adjacent cylindrical cells. Liquid droplets carried by streams are deposited on liquid membrane streams flowing along the fuel rod at the downstream of the spacer by the vortex streams. In view of the above, the liquid droplets can be deposited to the fuel rod without increasing the amount of metal of the spacer. Accordingly, the thermal margin of the fuel assembly can be improved without losing neutron economy. (I.N.)

  17. Fuel Cells

    DEFF Research Database (Denmark)

    Smith, Anders; Pedersen, Allan Schrøder

    2014-01-01

    Fuel cells have been the subject of intense research and development efforts for the past decades. Even so, the technology has not had its commercial breakthrough yet. This entry gives an overview of the technological challenges and status of fuel cells and discusses the most promising applications...... of the different types of fuel cells. Finally, their role in a future energy supply with a large share of fluctuating sustainable power sources, e.g., solar or wind, is surveyed....

  18. Fuel cycle

    International Nuclear Information System (INIS)

    Bahm, W.

    1989-01-01

    The situation of the nuclear fuel cycle for LWR type reactors in France and in the Federal Republic of Germany was presented in 14 lectures with the aim to compare the state-of-the-art in both countries. In addition to the momentarily changing fuilds of fuel element development and fueling strategies, the situation of reprocessing, made interesting by some recent developmnts, was portrayed and differences in ultimate waste disposal elucidated. (orig.) [de

  19. From Extended Nanofluidics to an Autonomous Solar-Light-Driven Micro Fuel-Cell Device.

    Science.gov (United States)

    Pihosh, Yuriy; Uemura, Jin; Turkevych, Ivan; Mawatari, Kazuma; Kazoe, Yutaka; Smirnova, Adelina; Kitamori, Takehiko

    2017-07-03

    Autonomous micro/nano mechanical, chemical, and biomedical sensors require persistent power sources scaled to their size. Realization of autonomous micro-power sources is a challenging task, as it requires combination of wireless energy supply, conversion, storage, and delivery to the sensor. Herein, we realized a solar-light-driven power source that consists of a micro fuel cell (μFC) and a photocatalytic micro fuel generator (μFG) integrated on a single microfluidic chip. The μFG produces hydrogen by photocatalytic water splitting under solar light. The hydrogen fuel is then consumed by the μFC to generate electricity. Importantly, the by-product water returns back to the photocatalytic μFG via recirculation loop without losses. Both devices rely on novel phenomena in extended-nano-fluidic channels that ensure ultra-fast proton transport. As a proof of concept, we demonstrate that μFG/μFC source achieves remarkable energy density of ca. 17.2 mWh cm -2 at room temperature. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Nuclear fuel

    International Nuclear Information System (INIS)

    Azevedo, J.B.L. de.

    1980-01-01

    All stages of nuclear fuel cycle are analysed with respect to the present situation and future perspectives of supply and demand of services; the prices and the unitary cost estimation of these stages for the international fuel market are also mentioned. From the world resources and projections of uranium consumption, medium-and long term analyses are made of fuel availability for several strategies of use of different reactor types. Finally, the cost of nuclear fuel in the generation of electric energy is calculated to be used in the energetic planning of the electric sector. (M.A.) [pt

  1. Fuel assembly

    International Nuclear Information System (INIS)

    Nomata, Terumitsu.

    1993-01-01

    Among fuel pellets to be loaded to fuel cans of a fuel assembly, fuel pellets having a small thermal power are charged in a region from the end of each of spacers up to about 50mm on the upstream of coolants that flow vertically at the periphery of fuel rods. Coolants at the periphery of fuel rods are heated by the heat generation, to result in voids. However, since cooling effect on the upstream of the spacers is low due to influences of the spacers. Further, since the fuel pellets disposed in the upstream region have small thermal power, a void coefficient is not increased. Even if a thermal power exceeding cooling performance should be generated, there is no worry of causing burnout in the upstream region. Even if burnout should be caused, safety margin and reliability relative to burnout are improved, to increase an allowable thermal power, thereby enabling to improve integrity and reliability of fuel rods and fuel assemblies. (N.H.)

  2. Fuel assembly

    International Nuclear Information System (INIS)

    Gjertsen, R.K.; Bassler, E.A.; Huckestein, E.A.; Salton, R.B.; Tower, S.N.

    1988-01-01

    A fuel assembly adapted for use with a pressurized water nuclear reactor having capabilities for fluid moderator spectral shift control is described comprising: parallel arranged elongated nuclear fuel elements; means for providing for axial support of the fuel elements and for arranging the fuel elements in a spaced array; thimbles interspersed among the fuel elements adapted for insertion of a rod control cluster therewithin; means for structurally joining the fuel elements and the guide thimbles; fluid moderator control means for providing a volume of low neutron absorbing fluid within the fuel assembly and for removing a substantially equivalent volume of reactor coolant water therefrom, a first flow manifold at one end of the fuel assembly sealingly connected to a first end of the moderator control tubes whereby the first ends are commonly flow connected; and a second flow manifold, having an inlet passage and an outlet passage therein, sealingly connected to a second end of the moderator control tubes at a second end of the fuel assembly

  3. Novel Nuclear Powered Photocatalytic Energy Conversion

    International Nuclear Information System (INIS)

    White, John R.; Kinsmen, Douglas; Regan, Thomas M.; Bobek, Leo M.

    2005-01-01

    The University of Massachusetts Lowell Radiation Laboratory (UMLRL) is involved in a comprehensive project to investigate a unique radiation sensing and energy conversion technology with applications for in-situ monitoring of spent nuclear fuel (SNF) during cask transport and storage. The technology makes use of the gamma photons emitted from the SNF as an inherent power source for driving a GPS-class transceiver that has the ability to verify the position and contents of the SNF cask. The power conversion process, which converts the gamma photon energy into electrical power, is based on a variation of the successful dye-sensitized solar cell (DSSC) design developed by Konarka Technologies, Inc. (KTI). In particular, the focus of the current research is to make direct use of the high-energy gamma photons emitted from SNF, coupled with a scintillator material to convert some of the incident gamma photons into photons having wavelengths within the visible region of the electromagnetic spectrum. The high-energy gammas from the SNF will generate some power directly via Compton scattering and the photoelectric effect, and the generated visible photons output from the scintillator material can also be converted to electrical power in a manner similar to that of a standard solar cell. Upon successful implementation of an energy conversion device based on this new gammavoltaic principle, this inherent power source could then be utilized within SNF storage casks to drive a tamper-proof, low-power, electronic detection/security monitoring system for the spent fuel. The current project has addressed several aspects associated with this new energy conversion concept, including the development of a base conceptual design for an inherent gamma-induced power conversion unit for SNF monitoring, the characterization of the radiation environment that can be expected within a typical SNF storage system, the initial evaluation of Konarka's base solar cell design, the design and

  4. Fuel element

    International Nuclear Information System (INIS)

    Kennedy, S.T.

    1982-01-01

    A nuclear reactor fuel element wherein a stack of nuclear fuel is prevented from displacement within its sheath by a retainer comprising a tube member which is radially expanded into frictional contact with the sheath by means of a captive ball within a tapered bore. (author)

  5. Nuclear fuel

    Energy Technology Data Exchange (ETDEWEB)

    Nakano, H [Power Reactor and Nuclear Fuel Development Corp., Tokyo (Japan)

    1976-10-01

    It is expected that nuclear power generation will reach 49 million kW in 1985 and 129 million kW in 1995, and the nuclear fuel having to be supplied and processed will increase in proportion to these values. The technical problems concerning nuclear fuel are presented on the basis of the balance between the benefit for human beings and the burden on the human beings. Recently, especially the downstream of nuclear fuel attracts public attention. Enriched uranium as the raw material for light water reactor fuel is almost monopolized by the U.S., and the technical information has not been published for fear of the diversion to nuclear weapons. In this paper, the present situations of uranium enrichment, fuel fabrication, transportation, reprocessing and waste disposal and the future problems are described according to the path of nuclear fuel cycle. The demand and supply of enriched uranium in Japan will be balanced up to about 1988, but afterwards, the supply must rely upon the early establishment of the domestic technology by centrifugal separation method. No problem remains in the fabrication of light water reactor fuel, but for the fabrication of mixed oxide fuel, the mechanization of the production facility and labor saving are necessary. The solution of the capital risk for the construction of the second reprocessing plant is the main problem. Japan must develop waste disposal techniques with all-out efforts.

  6. Fuel cells

    NARCIS (Netherlands)

    Veen, van J.A.R.; Janssen, F.J.J.G.; Santen, van R.A.

    1999-01-01

    The principles and present-day embodiments of fuel cells are discussed. Nearly all cells are hydrogen/oxygen ones, where the hydrogen fuel is usually obtained on-site from the reforming of methane or methanol. There exists a tension between the promise of high efficiency in the conversion of

  7. Fuel assembly

    International Nuclear Information System (INIS)

    Nakajima, Akiyoshi; Bessho, Yasunori; Aoyama, Motoo; Koyama, Jun-ichi; Hirakawa, Hiromasa; Yamashita, Jun-ichi; Hayashi, Tatsuo

    1998-01-01

    In a fuel assembly of a BWR type reactor in which a water rod of a large diameter is disposed at the central portion, the cross sectional area perpendicular to the axial direction comprises a region a of a fuel rod group facing to a wide gap water region to which a control rod is inserted, a region b of a fuel rod group disposed on the side of the wide gap water region other than the region a, a region d of a fuel rod group facing to a narrow gap water region and a region c of a fuel rod group disposed on the side of the narrow gap water region other than the region d. When comparing an amount of fission products contained in the four regions relative to that in the entire regions and average enrichment degrees of fuel rods for the four regions, the relative amount and the average enrichment degree of the fuel rod group of the region a is minimized, and the relative amount and the average enrichment degree of the fuel rod group in the region b is maximized. Then, reactor shut down margin during cold operation can be improved while flattening the power in the cross section perpendicular to the axial direction. (N.H.)

  8. Copper-organic/octamolybdates: structures, bandgap sizes, and photocatalytic activities.

    Science.gov (United States)

    Luo, Lan; Lin, Haisheng; Li, Le; Smirnova, Tatyana I; Maggard, Paul A

    2014-04-07

    The structures, optical bandgap sizes, and photocatalytic activities are described for three copper-octamolybdate hybrid solids prepared using hydrothermal methods, [Cu(pda)]4[β-Mo8O26] (I; pda = pyridazine), [Cu(en)2]2[γ-Mo8O26] (II; en = ethylenediamine), and [Cu(o-phen)2]2[α-Mo8O26] (III; o-phen = o-phenanthroline). The structure of I consists of a [Cu(pda)]4(4+) tetramer that bridges to neighboring [β-Mo8O26](4-) octamolybdate clusters to form two-dimensional layers that stack along the a axis. The previously reported structures of II and III are constructed from [Cu2(en)4Mo8O26] and [Cu2(o-phen)4Mo8O26] clusters. The optical bandgap sizes were measured by UV-vis diffuse reflectance techniques to be ∼1.8 eV for I, ∼3.1 eV for II, and ∼3.0 eV for III. Electronic structure calculations show that the smaller bandgap size of I originates primarily from an electronic transition between the valence and conduction band edges comprised of filled 3d(10) orbitals on Cu(I) and empty 4d(0) orbitals on Mo(VI). Both II and III contain Cu(II) and exhibit larger bandgap sizes. Accordingly, aqueous suspensions of I exhibit visible-light photocatalytic activity for the production of oxygen at a rate of ∼90 μmol O2 g(-1) h(-1) (10 mg samples; radiant power density of ∼1 W/cm(2)) and a turnover frequency per calculated surface [Mo8O26](4-) cluster of ∼36 h(-1). Under combined ultraviolet and visible-light irradiation, I also exhibits photocatalytic activity for hydrogen production in 20% aqueous methanol of ∼316 μmol H2 g(-1) h(-1). By contrast, II decomposed during the photocatalysis measurements. The molecular [Cu2(o-phen)4(α-Mo8O26)] clusters of III dissolve into the aqueous methanol solution under ultraviolet irradiation and exhibit homogeneous photocatalytic rates for hydrogen production of up to ∼8670 μmol H2·g(-1) h(-1) and a turnover frequency of 17 h(-1). The clusters of III can be precipitated out by evaporation and redispersed into solution with

  9. Photocatalytic Desulfurization of Waste Tire Pyrolysis Oil

    Directory of Open Access Journals (Sweden)

    Napida Hinchiranan

    2011-11-01

    Full Text Available Waste tire pyrolysis oil has high potential to replace conventional fossil liquid fuels due to its high calorific heating value. However, the large amounts of sulfurous compounds in this oil hinders its application. Thus, the aim of this research was to investigate the possibility to apply the photo-assisted oxidation catalyzed by titanium dioxide (TiO2, Degussa P-25 to partially remove sulfurous compounds in the waste tire pyrolysis oil under milder reaction conditions without hydrogen consumption. A waste tire pyrolysis oil with 0.84% (w/w of sulfurous content containing suspended TiO2 was irradiated by using a high-pressure mercury lamp for 7 h. The oxidized sulfur compounds were then migrated into the solvent-extraction phase. A maximum % sulfur removal of 43.6% was achieved when 7 g/L of TiO2 was loaded into a 1/4 (v/v mixture of pyrolysis waste tire oil/acetonitrile at 50 °C in the presence of air. Chromatographic analysis confirmed that the photo-oxidized sulfurous compounds presented in the waste tire pyrolysis oil had higher polarity, which were readily dissolved and separated in distilled water. The properties of the photoxidized product were also reported and compared to those of crude oil.

  10. Nuclear fuel

    International Nuclear Information System (INIS)

    Quinauk, J.P.

    1990-01-01

    Since 1985, Fragema has been marketing and selling the Advanced Fuel Assemby AFA whose main features are its zircaloy grids and removable top and bottom nozzles. It is this product, which exists for several different fuel assembly arrays and heights, that will be employed in the reactors at Daya Bay. Fragema employs gadolinium as the consumable poison to enable highperformance fuel management. More recently, the company has supplied fuel assemblies of the mixed-oxide(MOX) and enriched reprocessed uranium type. The reliability level of the fuel sold by Fragema is one of the highest in the world, thanks in particular to the excellence of the quality assurance and quality control programs that have been implemented at all stages of its design and manufacture

  11. Fuel assemblies

    International Nuclear Information System (INIS)

    Echigoya, Hironori; Nomata, Terumitsu.

    1983-01-01

    Purpose: To render the axial distribution relatively flat. Constitution: First nuclear element comprises a fuel can made of zircalloy i.e., the metal with less neutron absorption, which is filled with a plurality of UO 2 pellets and sealed by using a lower end plug, a plenum spring and an upper end plug by means of welding. Second fuel element is formed by substituting a part of the UO 2 pellets with a water tube which is sealed with water and has a space for allowing the heat expansion. The nuclear fuel assembly is constituted by using the first and second fuel elements together. In such a structure, since water reflects neutrons and decrease their leakage to increase the temperature, reactivity is added at the upper portion of the fuel assembly to thereby flatten the axial power distribution. Accordingly, stable operation is possible only by means of deep control rods while requiring no shallow control rods. (Sekiya, K.)

  12. Photocatalytic fabrics based on reduced graphene oxide and TiO{sub 2} coatings

    Energy Technology Data Exchange (ETDEWEB)

    Molina, J., E-mail: jamopue@doctor.upv.es [Departamento de Ingeniería Textil y Papelera, EPS de Alcoy, Universitat Politècnica de València, Plaza Ferrándiz y Carbonell s/n, 03801 Alcoy (Spain); Department of Textile Engineering, University of Minho, Azurém Campus, 4800-058 Guimarães (Portugal); Fernandes, F., E-mail: b6073@fisica.uminho.pt [Department Physics, University of Minho, Azurém Campus, 4800-058 Guimarães (Portugal); Fernández, J., E-mail: jaferse1@posgrado.upv.es [Departamento de Ingeniería Textil y Papelera, EPS de Alcoy, Universitat Politècnica de València, Plaza Ferrándiz y Carbonell s/n, 03801 Alcoy (Spain); Pastor, M., E-mail: marianapastor88@gmail.com [Department Physics, University of Minho, Azurém Campus, 4800-058 Guimarães (Portugal); Correia, A., E-mail: anacamcorreia@gmail.com [Department Physics, University of Minho, Azurém Campus, 4800-058 Guimarães (Portugal); Souto, A.P., E-mail: souto@det.uminho.pt [Department of Textile Engineering, University of Minho, Azurém Campus, 4800-058 Guimarães (Portugal); Carneiro, J.O., E-mail: carneiro@fisica.uminho.pt [Department Physics, University of Minho, Azurém Campus, 4800-058 Guimarães (Portugal); and others

    2015-09-15

    Graphical abstract: - Highlights: • Photocatalytic fabrics were produced with reduced graphene oxide (RGO) and TiO{sub 2}. • Charge transfer resistance decreased with the increasing number of RGO layers. • Scanning electrochemical microscopy showed the photoresponse obtained. • Photocatalytic properties were tested with Rhodamine B solutions. • Photocatalytic efficiency increased with the number of RGO layers. - Abstract: The purpose of this work is to obtain photocatalytic fabrics based on reduced graphene oxide (RGO) and TiO{sub 2} coatings on polyester fabrics. The influence of the applied number of RGO coatings on properties such as light absorption, conductivity, electroactivity and photocatalytic properties of the fabrics was established. An improvement of these properties with the number of RGO coatings applied was obtained. FESEM, EDX, XPS and FTIR-ATR showed the incorporation of the TiO{sub 2} nanoparticles on the fabrics. FTIR-ATR showed the formation of a bidentate carboxylic ligand with titanium atoms. The photocatalytic properties of the fabrics were tested with Rhodamine B dye solutions. Photocatalytic efficiency increased with the number of RGO coatings, due to the increased light absorption, and better electrical properties. The charge transfer resistance (R{sub ct}) and its time constant (τ) decreased, indicating a better electron transfer which helps to increase the lifetime of the pair electron/hole.

  13. Preparation and photocatalytic activity of chemically-bonded phosphate ceramics containing TiO2

    Science.gov (United States)

    Martins, Monize Aparecida; de Lima, Bruna de Oliveira; Ferreira, Leticia Patrício; Colonetti, Emerson; Feltrin, Jucilene; De Noni, Agenor

    2017-05-01

    Titanium dioxide was incorporated into chemically-bonded phosphate ceramic for use as photocatalytic inorganic coating. The coatings obtained were applied to unglazed ceramic tiles and cured at 350 °C. The surfaces were characterized by photocatalytic activity, determined in aqueous medium, based on the degradation of methylene blue dye. The effects of the percentage of TiO2 and the thickness of the layer on the photocatalytic efficiency were evaluated. The influence of the incorporation of TiO2 on the consolidation of the phosphate matrix coating was investigated using the wear resistance test. The crystalline phases of the coatings obtained were determined by XRD. The microstructure of the surfaces was analyzed by SEM. The thermal curing treatment did not cause a phase transition from anatase to rutile. An increase in the photocatalytic activity of the coating was observed with an increase in the TiO2 content. The dye degradation indices ranged from 14.9 to 44.0%. The photocatalytic efficiency was not correlated with the thickness of the coating layer deposited. The resistance to wear decreased with an increase in the TiO2 content. Comparison with a commercial photocatalytic ceramic coating indicated that there is a range of values for the TiO2 contents which offer potential for photocatalytic applications.

  14. Photocatalytic activity of titanium dioxide modified concrete materials - influence of utilizing recycled glass cullets as aggregates.

    Science.gov (United States)

    Chen, Jun; Poon, Chi-Sun

    2009-08-01

    Combining the use of photocatalysts with cementitious materials is an important development in the field of photocatalytic air pollution mitigation. This paper presents the results of a systematic study on assessing the effectiveness of pollutant degradation by concrete surface layers that incorporate a photocatalytic material - Titanium Dioxide. The photocatalytic activity of the concrete samples was determined by photocatalytic oxidation of nitric oxide (NO) in the laboratory. Recycled glass cullets, derived from crushed waste beverage bottles, were used to replace sand in preparing the concrete surface layers. Factors, which may affect the pollutant removal performance of the concrete layers including glass color, aggregate size and curing age, were investigated. The results show a significant enhancement of the photocatalytic activity due to the use of glass cullets as aggregates in the concrete layers. The samples fabricated with clear glass cullets exhibited threefold NO removal efficiency compared to the samples fabricated with river sand. The light transmittance property of glass was postulated to account for the efficiency improvement, which was confirmed by a separate simulation study. But the influence of the size of glass cullets was not evident. In addition, the photocatalytic activity of concrete surface layers decreased with curing age, showing a loss of 20% photocatalytic activity after 56-day curing.

  15. Defects improved photocatalytic ability of TiO2

    International Nuclear Information System (INIS)

    Li, Lei; Tian, Hong-Wei; Meng, Fan-Ling; Hu, Xiao-Ying; Zheng, Wei-Tao; Sun, Chang Q.

    2014-01-01

    Highlights: • Defect improves the photocatalytic ability by band gap narrowing and carrier life prolonging. • Atomic undercoordination shortens the local bonds, entraps, and polarizes electrons. • Polarization lowers the local workfunction and lengthens carrier life. • Entrapment and polarization narrows the band gap tuning the wavelength of absorption. - Abstract: Defect generation forms an important means modulating the photocatalytic ability of TiO 2 with mechanisms that remain yet unclear. Here we show that a spectral distillation clarifies the impact of defect on modulating the band gap, electroaffinity, and work function of the substance. Firstly, by analyzing XPS measurements, we calibrated the 2p 3/2 level of 451.47 eV for an isolated Ti atom and its shifts by 2.14 and 6.94 eV, respectively, upon Ti and TiO 2 bulk formation. Spectral difference between the defected and the un-defected TiO 2 skin revealed then that the 2p 3/2 level shifts further from 6.94 to 9.67 eV due to the defect-induced quantum entrapment. This entrapment is associated with an elevation of the upper edges of both the 2p 3/2 and the conduction band by polarization. The shortening and strengthening of bonds between undercoordinated atoms densify and entrap the core electrons, which in turn polarize the dangling bond electrons of defect atoms. The entrapment and polarization mediate thus the band gap, the electroaffinity, the work function, and the photocatalytic ability of TiO 2

  16. Photocatalytic Nanocomposites for the Protection of European Architectural Heritage

    Science.gov (United States)

    Roveri, Marco; Goidanich, Sara; Toniolo, Lucia

    2018-01-01

    In the field of stone protection, the introduction of inorganic nanoparticles, such as TiO2, ZnO, and Ag in polymeric blends can enhance the protective action of pristine treatments, as well as confer additional properties (photocatalytic, antifouling, and antibacterial). In the framework of the “Nano-Cathedral” European project, nanostructured photocatalytic protective treatments were formulated by using different TiO2 nanoparticles, solvents, and silane/siloxane systems in the blends. The results about the characterization and application of two promising nano-TiO2 based products applied on Apuan marble and Ajarte limestone are here reported, aiming at investigating the complex system “treatment/stone-substrate”. The nanocomposites show better performances when compared to a commercial reference siloxane based protective treatment, resulting in different performances once applied on different carbonatic substrates, with very low and high open porosity, confirming the necessity of correlating precisely the characteristics of the stone material to those of the protective formulations. In particular, the TiO2 photocatalytic behavior is strictly linked to the amount of available nanoparticles and to the active surface area. The alkyl silane oligomers of the water-based formulation have a good penetration into the microstructure of Ajarte limestone, whereas the solvent-based and small size monomeric formulation shows better results for Apuan marble, granting a good coverage of the pores. The encouraging results obtained so far in lab will be confirmed by monitoring tests aiming at assessing the effectiveness of the treatments applied in pilot sites of historical Gothic Cathedrals. PMID:29301338

  17. Hollow mesoporous titania microspheres: New technology and enhanced photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Zhenliang; Wei, Wenrui; Wang, Litong [School of Chemical Engineering, Fuzhou University, Fuzhou 350108 (China); Hong, Ruoyu, E-mail: rhong@suda.edu.cn [School of Chemical Engineering, Fuzhou University, Fuzhou 350108 (China); College of Chemistry, Chemical Engineering and Materials Science & Key Laboratory of Organic Synthesis of Jiangsu Province, Soochow University, SIP, Suzhou 215123 (China)

    2015-12-01

    Graphical abstract: Schematic of the formation process of HTS. - Highlights: • Amino modified porous PS-DVB microspheres were used as templates to coat TiO{sub 2.} • The coating of TiO{sub 2} was conducted under regular changing atmospheric pressure. • The PS-DVB@TiO{sub 2} was calcinated first under nitrogen and then under air to get HTS. • The resultant products were provided with high surface area and excellent photocatalytic activity under UV irradiation. - Abstract: Hollow titania microspheres (HTS) were fabricated via a sol–gel process by coating the hydrolysis product of titanium tetrabutoxide (TBOT) onto the amino (–NH{sub 2}) modified porous polystyrene cross-linked divinyl benzene (PS-DVB) microspheres under changing atmospheric pressure, followed by calcination in nitrogen and air atmosphere. Particularly, the atmospheric pressure was continuously and regularly changed during the formation process of PS-DVB@TiO{sub 2} microspheres. Then the TiO{sub 2} particles were absorbed into the pores and onto the surface of PS-DVB as well. The resultant HTS (around 2 μm in diameter) featured a high specific surface area (84.37 m{sup 2}/g), anatase crystal and stable hollow microsphere structure, which led to high photocatalysis activity. The photocatalytic degradation of malachite green (MG) organic dye solution was conducted under ultraviolet (UV) light irradiation, which showed a high photocatalytic ability (81% of MG was degraded after UV irradiation for 88 min). Therefore, it could be potentially applied for the treatment of wastewater contaminated by organic pollutants.

  18. Yttrium bismuth titanate pyrochlore mixed oxides for photocatalytic hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Merka, Oliver

    2012-10-18

    In this work, the sol-gel synthesis of new non-stoichiometric pyrochlore titanates and their application in photocatalytic hydrogen production is reported. Visible light response is achieved by introducing bismuth on the A site or by doping the B site by transition metal cations featuring partially filled d orbitals. This work clearly focusses on atomic scale structural changes induced by the systematical introduction of non-stoichiometry in pyrochlore mixed oxides and the resulting influence on the activity in photocatalytic hydrogen production. The materials were characterized in detail regarding their optical properties and their atomic structure. The pyrochlore structure tolerates tremendous stoichiometry variations. The non-stoichiometry in A{sub 2}O{sub 3} rich compositions is compensated by distortions in the cationic sub-lattice for the smaller Y{sup 3+} cation and by evolution of a secondary phase for the larger Bi{sup 3+} cation on the A site. For TiO{sub 2} rich compositions, the non-stoichiometry leads to a special vacancy formation in the A and optionally O' sites. It is shown that pyrochlore mixed oxides in the yttrium bismuth titanate system represent very active and promising materials for photocatalytic hydrogen production, if precisely and carefully tuned. Whereas Y{sub 2}Ti{sub 2}O{sub 7} yields stable hydrogen production rates over time, the bismuth richer compounds of YBiTi{sub 2}O{sub 7} and Bi{sub 2}Ti{sub 2}O{sub 7} are found to be not stable under irradiation. This drawback is overcome by applying a special co-catalyst system consisting of a precious metal core and a Cr{sub 2}O{sub 3} shell on the photocatalysts.

  19. Zinc vanadate nanorods and their visible light photocatalytic activity

    International Nuclear Information System (INIS)

    Pei, L.Z.; Lin, N.; Wei, T.; Liu, H.D.; Yu, H.Y.

    2015-01-01

    Highlights: • Zinc vanadate nanorods have been synthesized by a facile hydrothermal process. • The size of zinc vanadate nanorods can be controlled by growth conditions. • Zinc vanadate nanorods show good photocatalytic activities of methylene blue under solar light. - Abstract: Zinc vanadate nanorods have been synthesized by a simple hydrothermal process using zinc acetate and sodium vanadate as the raw materials. The zinc vanadate nanorods have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM) and solid UV–vis diffuse reflectance spectrum. XRD pattern and HRTEM image show that the zinc vanadate nanorods are composed of single crystalline monoclinic Zn 2 V 2 O 7 phase. SEM and TEM observations show that the diameter and length of the zinc vanadate nanorods are 50–100 nm and about 5 μm, respectively. Sodium dodecyl sulfonate (SDS) has an essential role in the formation of zinc vanadate nanorods. The SDS-assisted nucleation and growth process have been proposed to explain the formation and growth of the zinc vanadate nanorods. Solid UV–vis diffuse reflectance spectrum shows that the zinc vanadate nanorods have a band gap of 2.76 eV. The photocatalytic activities of the zinc vanadate nanorods have been evaluated by the photocatalytic degradation of methylene blue (MB) under solar light irradiation. The MB with the concentration of 10 mg L −1 can be degraded totally under the solar light irradiation for 4 h. It is suggested that the zinc vanadate nanorods exhibit promising application potential for the degradation of organic pollutants under solar light irradiation

  20. Method and compositions for producting optically clear photocatalytic coatings

    DEFF Research Database (Denmark)

    2009-01-01

    The invention relates to a method and compositions for producing a hydrophilic coating on a surface of a solid material. The method comprises a cleaning step and a coating step. The cleaning step may be preceded by an initial cleaning step and it may optionally be succeeded by a preconditioning...... step prior to the coating step. The cleaning step comprises cleaning and preconditioning a surface of a material by use of a first cleaning fluid composition comprising ceria (CeO2) particles. The coating step comprises treatment by use of a coating fluid composition comprising photocatalytically...

  1. On the mechanism of photocatalytic reactions with eosin Y

    Directory of Open Access Journals (Sweden)

    Michal Majek

    2014-04-01

    Full Text Available A combined spectroscopic, synthetic, and apparative study has allowed a more detailed mechanistic rationalization of several recently reported eosin Y-catalyzed aromatic substitutions at arenediazonium salts. The operation of rapid acid–base equilibria, direct photolysis pathways, and radical chain reactions has been discussed on the basis of pH, solvent polarity, lamp type, absorption properties, and quantum yields. Determination of the latter proved to be an especially valuable tool for the distinction between radical chain and photocatalytic reactions.

  2. Photocatalytic post-treatment in waste water reclamation systems

    Science.gov (United States)

    Cooper, Gerald; Ratcliff, Matthew A.; Verostko, Charles E.

    1989-01-01

    A photocatalytic water purification process is described which effectively oxidizes organic impurities common to reclaimed waste waters and humidity condensates to carbon dioxide at ambient temperatures. With this process, total organic carbon concentrations below 500 ppb are readily achieved. The temperature dependence of the process is well described by the Arrhenius equation and an activation energy barrier of 3.5 Kcal/mole. The posttreatment approach for waste water reclamation described here shows potential for integration with closed-loop life support systems.

  3. Design of micro-reactors and solar photocatalytic prototypes

    International Nuclear Information System (INIS)

    Flores E, R.M.; Hernandez H, M.; Perusquia del Cueto, M.R.; Bonifacio M, J.; Jimenez B, J.; Ortiz O, H.B.; Castaneda J, G.; Lugo H, M.

    2007-01-01

    In the ININ is carried out research in heterogeneous photocatalysis using artificial light for to degrade organic compounds. In this context, it is sought to use the solar radiation as energy source to knock down costs. Of equal form it requires to link the basic and applied research. For it, a methodology that allows to design and to build micro-reactors and plants pilot has been developed, like previous step, to request external supports and to a future commercialization. The beginning of these works gave place to the partial construction of a prototype of photocatalytic reactor of the cylinder-parabolic composed type (CPC)

  4. Surface spintronics enhanced photo-catalytic hydrogen evolution: Mechanisms, strategies, challenges and future

    Science.gov (United States)

    Zhang, Wenyan; Gao, Wei; Zhang, Xuqiang; Li, Zhen; Lu, Gongxuan

    2018-03-01

    Hydrogen is a green energy carrier with high enthalpy and zero environmental pollution emission characteristics. Photocatalytic hydrogen evolution (HER) is a sustainable and promising way to generate hydrogen. Despite of great achievements in photocatalytic HER research, its efficiency is still limited due to undesirable electron transfer loss, high HER over-potential and low stability of some photocatalysts, which lead to their unsatisfied performance in HER and anti-photocorrosion properties. In recent years, many spintronics works have shown their enhancing effects on photo-catalytic HER. For example, it was reported that spin polarized photo-electrons could result in higher photocurrents and HER turn-over frequency (up to 200%) in photocatalytic system. Two strategies have been developed for electron spin polarizing, which resort to heavy atom effect and magnetic induction respectively. Both theoretical and experimental studies show that controlling spin state of OHrad radicals in photocatalytic reaction can not only decrease OER over-potential (even to 0 eV) of water splitting, but improve stability and charge lifetime of photocatalysts. A convenient strategy have been developed for aligning spin state of OHrad by utilizing chiral molecules to spin filter photo-electrons. By chiral-induced spin filtering, electron polarization can approach to 74%, which is significantly larger than some traditional transition metal devices. Those achievements demonstrate bright future of spintronics in enhancing photocatalytic HER, nevertheless, there is little work systematically reviewing and analysis this topic. This review focuses on recent achievements of spintronics in photocatalytic HER study, and systematically summarizes the related mechanisms and important strategies proposed. Besides, the challenges and developing trends of spintronics enhanced photo-catalytic HER research are discussed, expecting to comprehend and explore such interdisciplinary research in

  5. Preparation of Hierarchical BiOBr Microspheres for Visible Light-Induced Photocatalytic Detoxification and Disinfection

    Directory of Open Access Journals (Sweden)

    Ayla Ahmad

    2016-01-01

    Full Text Available Photocatalytic degradation is a promising alternative to traditional wastewater treatment methods. Recently developed visible light-responsive photocatalyst, BiOBr, has attracted extensive attentions. Hereby, a detailed investigation of application of BiOBr to bacterial inactivation and organic pollutants degradation is reported. Hydrothermal catalyst was prepared using template-free method. While, for solvothermal synthesis, CTAB was used as a template. Results indicate a higher photocatalytic activity by the solvothermally prepared catalyst. Solvothermally prepared BiOBr exhibited high photocatalytic activities in both water detoxification and disinfection.

  6. Biosynthesis of Ag nanoparticles using pedicellamide and its photocatalytic activity: an eco-friendly approach.

    Science.gov (United States)

    Tamuly, Chandan; Hazarika, Moushumi; Bordoloi, Manobjyoti; Bhattacharyya, Pradip Kr; Kar, Rahul

    2014-11-11

    The synthesis of silver (Ag) nanoparticles using by pedicellamide (A), isolated from Piper pedicellatum C.DC leaf is demonstrated here. TEM analysis revealed that the Ag nanoparticles predominantly form spherical in shape. The compound 'A' act as a reducing, stabilizing and capping agent. The reaction mechanism was established by using density functional theory (DFT). Photocatalytic property of the Ag nanoparticles is investigated by degradation of Methyl Red (MR) dye under UV light. The kinetic, reaction mechanism and rate constant of photocatalytic degradation of MR was evaluated. The results show that Ag nanoparticles have suitable photocatalytic activity for the degradation of MR dye. Copyright © 2014 Elsevier B.V. All rights reserved.

  7. Application of zinc oxide fiber in the photocatalytic degradation of methyl orange

    International Nuclear Information System (INIS)

    Gerchman, D.; Alves, A.K.; Berutti, F.A.; Bergmann, C.P.

    2011-01-01

    In this work, zinc oxide fibers were obtained by electrospinning using polyvinylbutyral and zinc nitrate as precursors. After the synthesis, the material was heat treated at different temperatures to evaluate the effect of microstructure on its photocatalytic activity. The fibers obtained after heat treatment were characterized for morphology, phases, crystallinity and photocatalytic activity. The photocatalysis reaction was accompanied by the degradation of methyl orange in the presence of zinc oxide under UV illumination. It was observed that the crystallinity of zincite is a fundamental factor for the control of the photocatalytic activity of this material. (author)

  8. Preparation and photocatalytic property of potassium niobate K6Nb10.8O30

    International Nuclear Information System (INIS)

    Zhang Gaoke; Zou Xi; Gong Jie; He Fangsheng; Zhang Hao; Zhang Qiang; Liu Ying; Yang Xia; Hu Bo

    2006-01-01

    The TB-type potassium niobate K 6 Nb 10.8 O 30 was synthesized by a simple solid-state reaction method. Scanning electron microscope (SEM) and X-ray diffractometer (XRD) were used to characterize the structure of the photocatalyst. The photocatalyst K 6 Nb 10.8 O 30 shows high photocatalytic activity to photodegrade acid red G under UV irradiation. The influences of catalyst dosage, initial concentration of acid red G on the photocatalytic reaction were investigated. The kinetics of photocatalytic degradation of acid red G follows the first order kinetics

  9. Photocatalytic degradation of tartrazine dye using CuO straw-sheaf-like nanostructures.

    Science.gov (United States)

    Rao, Martha Purnachander; Wu, Jerry J; Asiri, Abdullah M; Anandan, Sambandam

    2017-03-01

    Straw-sheaf-like CuO nanostructures were fruitfully synthesized using a chemical precipitation approach for the photocatalytic degradation assessment of tartrazine. Phase identification, composition, and morphological outlook of prepared CuO nanostructures were established by X-ray diffraction and scanning electron microscopy analysis. The photocatalytic performance of the synthesized CuO nanostructures was appraised in the presence of visible light and the possible intermediates formed during the photocatalytic degradation were analyzed by gas chromatography-mass spectrometry. A suitable degradation pathway has also been proposed.

  10. Insights into highly improved solar-driven photocatalytic oxygen evolution over integrated Ag3PO4/MoS2 heterostructures

    Science.gov (United States)

    Cui, Xingkai; Yang, Xiaofei; Xian, Xiaozhai; Tian, Lin; Tang, Hua; Liu, Qinqin

    2018-04-01

    Oxygen evolution has been considered as the rate-determining step in photocatalytic water splitting due to its sluggish four-electron half-reaction rate, the development of oxygen-evolving photocatalysts with well-defined morphologies and superior interfacial contact is highly important for achieving high-performance solar water splitting. Herein, we report the fabrication of Ag3PO4/MoS2 nanocomposites and, for the first time, their use in photocatalytic water splitting into oxygen under LED light illumination. Ag3PO4 nanoparticles were found to be anchored evenly on the surface of MoS2 nanosheets, confirming an efficient hybridization of two semiconductor materials. A maximum oxygen-generating rate of 201.6 mol L-1 g-1 h-1 was determined when 200 mg MoS2 nanosheets were incorporated into Ag3PO4 nanoparticles, which is around 5 times higher than that of bulk Ag3PO4. Obvious enhancements in light-harvesting property, as well as electron-hole separation and charge transportation are revealed by the combination of different characterizations. ESR analysis verified that more active oxygen-containing radicals generate over illuminated Ag3PO4/MoS2 composite photocatalysts rather than irradiated Ag3PO4. The improvement in oxygen evolution performance of Ag3PO4/MoS2 composite photocatalysts is ascribed to wide spectra response in the visible-light region, more efficient charge separation and enhanced oxidation capacity in the valence band (VB). This study provides new insights into the design and development of novel composite photocatalytic materials for solar-to-fuel conversion.

  11. Fabrication of modified g-C3N4 nanorod/Ag3PO4 nanocomposites for solar-driven photocatalytic oxygen evolution from water splitting

    Science.gov (United States)

    Tian, Lin; Xian, Xiaozhai; Cui, Xingkai; Tang, Hua; Yang, Xiaofei

    2018-02-01

    Semiconductor-based photocatalysis has been considered as one of the most effective techniques to achieve the conversion of clean and sustainable sunlight to solar fuel, in which the construction of novel solar-driven photocatalytic systems is the key point. Here, we report initially the synthesis of modified graphitic carbon nitride (g-C3N4) nanorods via the calcination of intermediates obtained from the co-polymerization of precursors, and the in-situ hybridization of Ag3PO4 with as-prepared modified g-C3N4 to produce g-C3N4 nanorod/Ag3PO4 composite materials. The diameter of modified rod-like g-C3N4 materials is determined to be around 1 μm. Subsequently the morphological features, crystal and chemical structures of the assembled g-C3N4 nanorod/Ag3PO4 composites were systematically investigated by SEM, XRD, XPS, UV-vis diffuse reflectance spectra (DRS). Furthermore, the use of as-prepared composite materials as the catalyst for photocatalytic oxygen evolution from water splitting was studied. The oxygen-generating results showed that the composite photocatalyst modified with 600 mg rod-like g-C3N4 demonstrates 2.5 times higher efficiency than that of bulk Ag3PO4. The mechanism behind the enhancement in the oxygen-evolving activity is proposed on the basis of in-situ electron spin resonance (ESR) measurement as well as theoretical analysis. The study provides new insights into the design and development of new photocatalytic composite materials for energy and environmental applications.

  12. Fuel cells:

    DEFF Research Database (Denmark)

    Sørensen, Bent

    2013-01-01

    A brief overview of the progress in fuel cell applications and basic technology development is presented, as a backdrop for discussing readiness for penetration into the marketplace as a solution to problems of depletion, safety, climate or environmental impact from currently used fossil and nucl......A brief overview of the progress in fuel cell applications and basic technology development is presented, as a backdrop for discussing readiness for penetration into the marketplace as a solution to problems of depletion, safety, climate or environmental impact from currently used fossil...... and nuclear fuel-based energy technologies....

  13. Fuel assemblies

    International Nuclear Information System (INIS)

    Nakatsuka, Masafumi.

    1979-01-01

    Purpose: To prevent scattering of gaseous fission products released from fuel assemblies stored in an fbr type reactor. Constitution; A cap provided with means capable of storing gas is adapted to amount to the assembly handling head, for example, by way of threading in a storage rack of spent fuel assemblies consisting of a bottom plate, a top plate and an assembly support mechanism. By previously eliminating the gas inside of the assembly and the cap in the storage rack, gaseous fission products upon loading, if released from fuel rods during storage, are stored in the cap and do not scatter in the storage rack. (Horiuchi, T.)

  14. Preparation of TiO{sub 2} nanotubes, study of their morphology and photocatalytic properties; Priprava nanotrubiek TiO{sub 2}, studium ich morfologie a fotokatalytickych vlastnosti

    Energy Technology Data Exchange (ETDEWEB)

    Motola, M.; Plasch, G. [Univerzita Komenskeho, Prirodovedecka fakulta, Katedra anorganickej chemie, 84215 Bratislava (Slovakia); Satrapinskyy, L. [Univerzita Komenskeho, Fakulta matematiky, fyziky a informatiky, Katedra experimentalnej fyziky, 84248 Bratislava (Slovakia)

    2013-04-16

    The present paper deals with the synthesis and characterization of titanium dioxide nanotubes (TNTs) for photocatalytic applications. Nanotubes were prepared by electrochemical anodic oxidation. The samples were heat treated by annealing to become photocatalytically active. Using scanning electron microscopy morphology of the nanotubes was studied. Phase composition of samples was measured by X-ray diffraction (XRD). The photocatalytic activity of nanotubes leads to decrease of the concentration of Rhodamine B during irradiation with UV A light. The photocatalytic activity of nanotubes was compared with the photocatalytic activity of Aeroxide P25 nanocrystalline titania powder. The best photocatalytic active show the samples annealed at 400 grad C. (authors)

  15. Controlled synthesis of bismuth oxyiodide toward optimization of photocatalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Liao, Chenxing; Ma, Zhijun [State Key Laboratory of Luminescent Materials and Devices, School of Materials Science and Engineering, South China University of Technology, Wushan Road 381, Guangzhou 510641 (China); Chen, Xiaofeng, E-mail: chenxf@scut.edu.c [Biomaterials Research Institute, School of Materials Science and Engineering, South China University of Technology, Wushan Road 381, Guangzhou 510641 (China); He, Xin [School of Applied Physics and Materials, Wuyi University, Jiangmen 529020 (China); Qiu, Jianrong, E-mail: qjr@scut.edu.cn [State Key Laboratory of Luminescent Materials and Devices, School of Materials Science and Engineering, South China University of Technology, Wushan Road 381, Guangzhou 510641 (China)

    2016-11-30

    Highlights: • Different bismuth oxyiodide was synthesized. • The hollow Bi{sub 4}O{sub 5}I{sub 2} microspheres was obtained. • Formation mechanism of the hollow structure was discussed in detail. - Abstract: A new investigation on the variation rule of the structure, morphology, chemical composition and photocatalytic performance of bismuth oxyiodide synthesized by solvothermal method as a function of reaction conditions was performed here. The composition and morphology of the product could be determined by X-ray diffraction, thermogravimetric analysis and scanning electron microscopy. The results revealed that the particle size together with content of iodide in bismuth oxyiodide decrease with the increase of the concentration of reaction precursors. Hollow Bi{sub 4}O{sub 5}I{sub 2} microsphere with specific surface area as high as 120.88 m{sup 2} g{sup −1} can be easily synthesized when the concentration of the reaction precursors finally increased to 62.5 mM. Photocatalytic water purification performance of the as-prepared samples was evaluated by using Rhodamine B (RhB) as a model contaminant. The results revealed that the hollow Bi{sub 4}O{sub 5}I{sub 2} exhibited the best performance among all the bismuth oxyodide synthesized here for the degradation of RhB under visible light irradiation. Meanwhile, the formation mechanism of the hierarchical hollow structure of bismuth oxyiodide was investigated by the dissolution-recrystallization mechanism.

  16. Integrated photocatalytic filtration array for indoor air quality control.

    Science.gov (United States)

    Denny, Frans; Permana, Eric; Scott, Jason; Wang, Jing; Pui, David Y H; Amal, Rose

    2010-07-15

    Photocatalytic and filtration technologies were integrated to develop a hybrid system capable of removing and oxidizing organic pollutants from an air stream. A fluidized bed aerosol generator (FBAG) was adapted to prepare TiO(2)-loaded ventilation filters for the photodegradation of gas phase ethanol. Compared to a manually loaded filter, the ethanol photodegradation rate constant for the FBAG coated filter increased by 361%. Additionally, the presence of the photogenerated intermediate product, acetaldehyde, was reduced and the time for mineralization to CO(2) was accelerated. These improvements were attributed to the FBAG system providing a more uniform distribution of TiO(2) particles across the filter surface leading to greater accessibility by the UV light. A dual-UV-lamp system, as opposed to a single-lamp system, enhanced photocatalytic filter performance demonstrating the importance of high light irradiance and light distribution across the filter surface. Substituting the blacklight blue lamps with a UV-light-emitting-diode (UV-LED) array led to further improvement as well as suppressed the electrical energy per order (EE/O) by a factor of 6. These improvements derived from the more uniform distribution of light irradiance as well as the higher efficiency of UV-LEDs in converting electrical energy to photons.

  17. Nanostructured porous ZnO film with enhanced photocatalytic activity

    International Nuclear Information System (INIS)

    Wang Lina; Zheng Yingying; Li Xiaoyun; Dong Wenjun; Tang Weihua; Chen Benyong; Li Chaorong; Li Xiao; Zhang Tierui

    2011-01-01

    Well-defined ZnO nanostructured films have been fabricated directly on Zn foil via hydrothermal synthesis. During the fabrication of the ZnO nanostructured films, the Zn foil serves as the Zn source and also the substrate. Porous nanosheet-based, nanotube-based and nanoflower-based ZnO films can all be easily prepared by adjusting the alkali type, reaction time and reaction temperature. The composition, morphology and structure of ZnO films are characterized by X-ray diffraction, scanning electron microscope and high-resolution transmission electron microscope. The porous ZnO nanosheet-based film exhibits enhanced photocatalytic activity in the degradation of Rhodamine B under UV light irradiation. This can be attributed to the high surface area of the ZnO nanosheet and the large percentage of the exposed [001] facet. Moreover, the self-supporting, recyclable and stable ZnO photocatalytic film can be readily recovered and potentially applied for pollution disposal.

  18. Photocatalytic and Photoelectrochemical Water Splitting by Inorganic Materials

    KAUST Repository

    Deng, Xiaohui

    2012-12-01

    Hydrogen has been identified as a potential energy carrier due to its high energy capacity and environmental harmlessness. Compared with hydrogen production from hydrocarbons such as methane and naphtha in a conventional hydrogen energy system, photocatalytic hydrogen evolution from water splitting offers a more economic approach since it utilizes the abundant solar irradiation as energy source and water as initial reactant. Powder photocatalyst, which generates electrons and holes under illumination, is the origin where the overall reaction happens. High solar energy conversion efficiency especially from visible range is commonly the target. Besides, cocatalyst for hydrogen and oxygen evolution is also playing an essential role in facilitating the charge separation and enhancing the kinetics. In this thesis, the objective is to achieve high energy conversion efficiency towards water splitting from diverse aspects. The third chapter focuses on a controllable method to fabricate metal pattern, which is candidate for hydrogen evolution cocatalyst while chapter 4 is on the combination of strontium titanium oxide (SrTiO3) with graphene oxide (GO) for a better photocatalytic performance. In the last chapter, photoelectrochemical water splitting by Ta3N5 photoanode and FeOOH as a novel oxygen evolution cocatalyst has been investigated.

  19. Effect of photocatalytic and hydrophobic coatings on brewery surface microorganisms.

    Science.gov (United States)

    Priha, O; Laakso, J; Tapani, K; Levänen, E; Kolari, M; Mäntylä, T; Storgårds, E

    2011-11-01

    The aim of this study was to determine whether process hygiene in the beverage industry could be improved by applying new coating techniques to process surfaces. Photocatalytic titanium dioxide (TiO(2)) and hydrophobic coatings applied to stainless steel with or without added antimicrobial compounds were studied in laboratory attachment tests and in a 15-month process study. No clear reductions in numbers of attached microbes were obtained with photocatalytic coatings, except for coatings to which silver had been added. These TiO(2)+Ag coatings reduced microbial coverage in laboratory studies and in some process samples. Hydrophobic coatings reduced the area coverage of microorganisms in 4-h laboratory studies but did not affect colony counts in laboratory or process studies. The surfaces had changed from hydrophobic into hydrophilic during the process study. The coatings did not mechanically fully withstand process conditions; part of the hydrophobic coatings had peeled off, most of the precipitated Ag had dissolved, and some of the TiO(2) coatings were damaged. In conclusion, functional coatings have potential for reducing microbial loads on beverage industry surfaces, but these coatings need further development.

  20. Synthesis and photocatalytic activity of poly(triazine imide)

    KAUST Repository

    Ham, Yeilin

    2012-10-22

    Poly(triazine imide) was synthesized with incorporation of Li+ and Cl- ions (PTI/Li+Cl-) to form a carbon nitride derivative. The synthesis of this material by the temperature-induced condensation of dicyandiamide was examined both in a eutectic mixture of LiCl-KCl and without KCl. On the basis of X-ray diffraction measurements of the synthesized materials, we suggest that a stoichiometric amount of LiCl is necessary to obtain the PTI/Li+Cl- phase without requiring the presence of KCl at 873 K. PTI/Li+Cl- with modification by either Pt or CoOx as cocatalyst photocatalytically produced H2 or O2, respectively, from water. The production of H2 or O2 from water indicates that the valence and conduction bands of PTI/Li+Cl- were properly located to achieve overall water splitting. The treatment of PTI/Li +Cl- with [Pt(NH3)4]2+ cations enabled the deposition of Pt through ion exchange, demonstrating photocatalytic activity for H2 evolution, while treatment with [PtCl6]2- anions resulted in no Pt deposition. This was most likely because of the preferential exchange between Li+ ions and [Pt(NH3)4]2+ cations. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Functionalized nanostructures for enhanced photocatalytic performance under solar light

    Directory of Open Access Journals (Sweden)

    Liejin Guo

    2014-07-01

    Full Text Available Photocatalytic hydrogen production from water has been considered to be one of the most promising solar-to-hydrogen conversion technologies. In the last decade, various functionalized nanostructures were designed to address the primary requirements for an efficient photocatalytic generation of hydrogen by using solar energy: visible-light activity, chemical stability, appropriate band-edge characteristics, and potential for low-cost fabrication. Our aim is to present a short review of our recent attempts that center on the above requirements. We begin with a brief introduction of photocatalysts coupling two or more semiconductors, followed by a further discussion of the heterostructures with improved matching of both band structures and crystal lattices. We then elaborate on the heterostructure design of the targeted materials from macroscopic regulation of compositions and phases, to the more precise control at the nanoscale, i.e., materials with the same compositions but different phases with certain band alignment. We conclude this review with perspectives on nanostructure design that might direct future research of this technology.

  2. Photocatalytic and electrochemical combined treatment of textile wash water

    International Nuclear Information System (INIS)

    Neelavannan, M.G.; Revathi, M.; Ahmed Basha, C.

    2007-01-01

    Various chemical and physical processes for treatment of textile effluent are not destructive but they only transfer the contaminants from one form to another. The presence of high concentration of organic dye and total dissolved solids (TDS) in the effluent that are not removed by biological treatment must be eliminated by an alternative method to the conventional ones is the advanced oxidation process (AOP). A procion blue dye effluent was treated by photo and electrochemical oxidation process as well as by combining photocatalytic degradation using TiO 2 suspensions. Chemical oxygen demand (COD) and colour removal can be used to follow the degradation of the organic pollutant. The effects of pH, current density, flow rate of effluent that passes into the reactor and supporting electrolyte were studied. Comparative studies were carried out on photocatalytic and electrochemical process to degrade the procion blue. The maximum COD reduction and colour removal were 96 and 100%, respectively. Photodegradation efficiency of dye was high when photolysis was carried out in the presence of 40 mg/l of TiO 2

  3. Synthesis and photocatalytic activity of poly(triazine imide)

    KAUST Repository

    Ham, Yeilin; Maeda, Kazuhiko; Cha, Dong Kyu; Takanabe, Kazuhiro; Domen, Kazunari

    2012-01-01

    Poly(triazine imide) was synthesized with incorporation of Li+ and Cl- ions (PTI/Li+Cl-) to form a carbon nitride derivative. The synthesis of this material by the temperature-induced condensation of dicyandiamide was examined both in a eutectic mixture of LiCl-KCl and without KCl. On the basis of X-ray diffraction measurements of the synthesized materials, we suggest that a stoichiometric amount of LiCl is necessary to obtain the PTI/Li+Cl- phase without requiring the presence of KCl at 873 K. PTI/Li+Cl- with modification by either Pt or CoOx as cocatalyst photocatalytically produced H2 or O2, respectively, from water. The production of H2 or O2 from water indicates that the valence and conduction bands of PTI/Li+Cl- were properly located to achieve overall water splitting. The treatment of PTI/Li +Cl- with [Pt(NH3)4]2+ cations enabled the deposition of Pt through ion exchange, demonstrating photocatalytic activity for H2 evolution, while treatment with [PtCl6]2- anions resulted in no Pt deposition. This was most likely because of the preferential exchange between Li+ ions and [Pt(NH3)4]2+ cations. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Intrinsic photocatalytic assessment of reactively sputtered TiO₂ films.

    Science.gov (United States)

    Rafieian, Damon; Driessen, Rick T; Ogieglo, Wojciech; Lammertink, Rob G H

    2015-04-29

    Thin TiO2 films were prepared by DC magnetron reactive sputtering at different oxygen partial pressures. Depending on the oxygen partial pressure during sputtering, a transition from metallic Ti to TiO2 was identified by spectroscopic ellipsometry. The crystalline nature of the film developed during a subsequent annealing step, resulting in thin anatase TiO2 layers, displaying photocatalytic activity. The intrinsic photocatalytic activity of the catalysts was evaluated for the degradation of methylene blue (MB) using a microfluidic reactor. A numerical model was employed to extract the intrinsic reaction rate constants. High conversion rates (90% degradation within 20 s residence time) were observed within these microreactors because of the efficient mass transport and light distribution. To evaluate the intrinsic reaction kinetics, we argue that mass transport has to be accounted for. The obtained surface reaction rate constants demonstrate very high reactivity for the sputtered TiO2 films. Only for the thinnest film, 9 nm, slightly lower kinetics were observed.

  5. Photocatalytically active titanium dioxide nanopowders: Synthesis, photoactivity and magnetic separation

    International Nuclear Information System (INIS)

    Nikkanen, J-P; Heinonen, S; Saarivirta, E Huttunen; Honkanen, M; Levänen, E

    2013-01-01

    Two approaches were used to obtain nanocrystalline titanium dioxide (TiO 2 ) photocatalyst powders. Firstly, low-temperature synthesis method and secondly liquid flame spraying. The structural properties of the produced powders were determined with X-ray diffraction, transmission electron microscopy and nitrogen adsorption tests. The photocatalytic properties of the powders were studied with methylene blue (MB) discoloration tests. After discolorations tests, TiO 2 was coagulated with magnetite particles using FeCl 3 ·6 H 2 O at a fixed pH value. Magnetic separation of coagulated TiO 2 and magnetite was carried out by a permanent magnet. The obtained results showed that the particle size of the powders synthesized at low-temperature was very small and the specific surface area high. The phase content of the powder was also shown to depend greatly on the acidity of the synthesis solution. Powder synthesized by liquid flame spraying was mixture of anatase and rutile phases with essentially larger particle size and lower specific surface area than those of low-temperature synthesized powders. The MB discoloration test showed that photocatalytic activity depends on the phase structure as well as the specific surface area of the synthesized TiO 2 powder. The magnetic separation of TiO 2 –magnetite coagulate from solution proved to be efficient around pH:8

  6. Fuel behaviour

    International Nuclear Information System (INIS)

    Fodor, M.; Matus, L.; Vigassy, J.

    1987-11-01

    A short summary of the main critical points in fuel performance of nuclear power reactors from chemical and mechanical point of view is given. A schedule for a limited research program is included. (author) 17 refs

  7. Fuel cells

    International Nuclear Information System (INIS)

    Niederdoeckl, J.

    2001-01-01

    Europe has at present big hopes on the fuel cells technology, in comparison with other energy conversion technologies, this technology has important advantages, for example: high efficiency, very low pollution and parallel use of electric and thermal energy. Preliminary works for fuel cells developing and its commercial exploitation are at full speed; until now the European Union has invested approx. 1.7 billion Schillings, 60 relevant projects are being executed. The Austrian industry is interested in applying this technique to drives, thermal power stations and the miniature fuel cells as replacement of batteries in electronic products (Notebooks, mobile telephones, etc.). A general description of the historic development of fuel cells including the main types is given as well as what is the situation in Austria. (nevyjel)

  8. Fuel assembly

    International Nuclear Information System (INIS)

    Ishibashi, Yoko; Aoyama, Motoo; Oyama, Jun-ichi.

    1995-01-01

    Burnable poison-incorporating fuel rods of a first group are disposed in a region in adjacent with a water rod having a large diameter (neutron moderator rod) disposed to the central portion of a fuel assembly. Burnable poison-incorporating fuel rods of a second group are disposed to a region other than peripheral zone in adjacent with a channel box and corners positioned at an inner zone, in adjacent with the channel box. The average concentration of burnable poisons of the burnable poison-incorporating fuel rods of the first group is made greater than that of the second group. With such a constitution, when the burnable poisons of the first group are burnt out, the burnable poisons of the second group are also burnt out at the same time. Accordingly, an amount of burnable poisons left unburnt at the final stage of the operation cycle is reduced, to improve the reactivity. This can improve the economical property. (I.N.)

  9. Fuel element

    International Nuclear Information System (INIS)

    Armijo, J.S.

    1976-01-01

    A fuel element for nuclear reactors is proposed which has a higher corrosion resisting quality in reactor operations. The zirconium alloy coating around the fuel element (uranium or plutonium compound) has on its inside a protection layer of metal which is metallurgically bound to the substance of the coating. As materials are namned: Alluminium, copper, niobium, stainless steel, and iron. This protective metallic layer has another inner layer, also metallurgically bound to its surface, which consists usually of a zirconium alloy. (UWI) [de

  10. Fuel assembly

    International Nuclear Information System (INIS)

    Ueda, Sei; Ando, Ryohei; Mitsutake, Toru.

    1995-01-01

    The present invention concerns a fuel assembly suitable to a BWR-type reactor and improved especially with the nuclear characteristic, heat performance, hydraulic performance, dismantling or assembling performance and economical property. A part of poison rods are formed as a large-diameter/multi-region poison rods having a larger diameter than a fuel rod. A large number of fuel rods are disposed surrounding a large diameter water rod and a group of the large-diameter/multi-region poison rods in adjacent with the water rod. The large-diameter water rod has a burnable poison at the tube wall portion. At least a portion of the large-diameter poison rods has a coolant circulation portion allowing coolants to circulate therethrough. Since the large-diameter poison rods are disposed at a position of high neutron fluxes, a large neutron multiplication factor suppression effect can be provided, thereby enabling to reduce the number of burnable poison rods relative to fuels. As a result, power peaking in the fuel assembly is moderated and a greater amount of plutonium can be loaded. In addition the flow of cooling water which tends to gather around the large diameter water rod can be controlled to improve cooling performance of fuels. (N.H.)

  11. Magnetically separable CuFe{sub 2}O{sub 4}/AgBr composite photocatalysts: Preparation, characterization, photocatalytic activity and photocatalytic mechanism under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Yalei; Lin, Cuiping; Bi, Huijie; Liu, Yonggang; Yan, Qishe, E-mail: Qisheyanzzu@163.com

    2017-01-15

    Highlights: • CuFe{sub 2}O{sub 4}/AgBr composites were prepared by a facile sol-gel and hydrothermal method. • Visible-light response and high photocatalytic performance. • Excellent magnetic properties. • Different reactive species had different effects on degradation different pollutants. - Abstract: The CuFe{sub 2}O{sub 4} and CuFe{sub 2}O{sub 4}/AgBr composites with different CuFe{sub 2}O{sub 4} contents were prepared by a facile sol-gel and hydrothermal method, respectively. The as-synthesized photocatalysts were characterized by means of powder X-ray diffraction (XRD), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), and UV–vis diffuse reflectance spectrum (UV–vis DRS). Their magnetic properties, photocatalytic degradation activities on methyl orange (MO) and tetracycline hydrochloride (TC) solution and photocatalytic mechanism were investigated in detail. The results revealed that the CuFe{sub 2}O{sub 4}/AgBr composites exhibited significantly higher photocatalytic activities than the pure CuFe{sub 2}O{sub 4}. The enhanced photocatalytic activity could be attributed to the matched band structure of two components and more effective charge transportation and separations. In addition, the quenching investigation of different scavengers demonstrated that h{sup +}, ·OH, ·O{sub 2}{sup −} reactive species played different roles in the decolorization of MO and degradation of TC.

  12. Artificial photosynthesis for production of hydrogen peroxide and its fuel cells.

    Science.gov (United States)

    Fukuzumi, Shunichi

    2016-05-01

    The reducing power released from photosystem I (PSI) via ferredoxin enables the reduction of NADP(+) to NADPH, which is essential in the Calvin-Benson cycle to make sugars in photosynthesis. Alternatively, PSI can reduce O2 to produce hydrogen peroxide as a fuel. This article describes the artificial version of the photocatalytic production of hydrogen peroxide from water and O2 using solar energy. Hydrogen peroxide is used as a fuel in hydrogen peroxide fuel cells to make electricity. The combination of the photocatalytic H2O2 production from water and O2 using solar energy with one-compartment H2O2 fuel cells provides on-site production and usage of H2O2 as a more useful and promising solar fuel than hydrogen. This article is part of a Special Issue entitled Biodesign for Bioenergetics--The design and engineering of electronc transfer cofactors, proteins and protein networks, edited by Ronald L. Koder and J.L. Ross Anderson. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Laboratory and field studies of photocatalytic NOx and O3 removal by coatings on concrete.

    Science.gov (United States)

    2017-03-01

    This project involved thorough testing of titanium dioxide (TiO2)-containing commercial photocatalytic coatings : applied to portland cement concrete for highway applications, focusing on the use of these coatings as an : abatement method for atmosph...

  14. Photocatalytic properties of chemically grown vanadium oxide at 65 °C

    Energy Technology Data Exchange (ETDEWEB)

    Vernardou, D., E-mail: dimitra@iesl.forth.gr [Center of Materials Technology and Photonics, School of Applied Technology, Technological Educational Institute of Crete, 710 04 Heraklion, Crete (Greece); Science Department, School of Applied Technology, Technological Educational Institute of Crete, 710 04 Heraklion, Crete (Greece); Drosos, H.; Fasoulas, J. [Mechanical Engineering Department, School of Applied Technology, Technological Educational Institute of Crete, 710 04 Heraklion, Crete (Greece); Koudoumas, E. [Center of Materials Technology and Photonics, School of Applied Technology, Technological Educational Institute of Crete, 710 04 Heraklion, Crete (Greece); Electrical Engineering Department, School of Applied Technology, Technological Educational Institute of Crete, 710 04 Heraklion, Crete (Greece); Katsarakis, N. [Center of Materials Technology and Photonics, School of Applied Technology, Technological Educational Institute of Crete, 710 04 Heraklion, Crete (Greece); Science Department, School of Applied Technology, Technological Educational Institute of Crete, 710 04 Heraklion, Crete (Greece); Institute of Electronic Structure and Laser, Foundation for Research and Technology—Hellas, P.O. Box 1527, Vassilika Vouton, 711 10 Heraklion, Crete (Greece)

    2014-03-31

    In this paper, the photocatalytic response of amorphous V{sub 2}O{sub 5} coatings prepared by hydrothermal growth at 65 °C is presented. The position of the substrate during the deposition and the pH of the solution were found to affect the coverage and the response of the coatings upon catalysis. The photocatalytic activity of the coatings was tested using stearic acid as a pollutant for an illumination time of 480 min. The materials grown on microscope glass positioned at an angle of 0° with respect to the bottom of the bottle exhibit the best photocatalytic activity, degrading stearic acid by 64% due to the enhanced surface coverage. - Highlights: • Hydrothermally grown amorphous V{sub 2}O{sub 5} coatings at 65 °C • Their properties are dependent on the substrate arrangement. • Their photocatalytic activity is correlated with the oxide coverage.

  15. Harvesting solar light with crystalline carbon nitrides for efficient photocatalytic hydrogen evolution

    KAUST Repository

    Bhunia, Manas Kumar; Yamauchi, Kazuo; Takanabe, Kazuhiro

    2014-01-01

    Described herein is the photocatalytic hydrogen evolution using crystalline carbon nitrides (CNs) obtained by supramolecular aggregation followed by ionic melt polycondensation (IMP) using melamine and 2,4,6-triaminopyrimidine as a dopant. The solid

  16. Photocatalytic properties of chemically grown vanadium oxide at 65 °C

    International Nuclear Information System (INIS)

    Vernardou, D.; Drosos, H.; Fasoulas, J.; Koudoumas, E.; Katsarakis, N.

    2014-01-01

    In this paper, the photocatalytic response of amorphous V 2 O 5 coatings prepared by hydrothermal growth at 65 °C is presented. The position of the substrate during the deposition and the pH of the solution were found to affect the coverage and the response of the coatings upon catalysis. The photocatalytic activity of the coatings was tested using stearic acid as a pollutant for an illumination time of 480 min. The materials grown on microscope glass positioned at an angle of 0° with respect to the bottom of the bottle exhibit the best photocatalytic activity, degrading stearic acid by 64% due to the enhanced surface coverage. - Highlights: • Hydrothermally grown amorphous V 2 O 5 coatings at 65 °C • Their properties are dependent on the substrate arrangement. • Their photocatalytic activity is correlated with the oxide coverage

  17. Photocatalytic Membrane Reactor for the Removal of C.I. Disperse Red 73

    Directory of Open Access Journals (Sweden)

    Valentina Buscio

    2015-06-01

    Full Text Available After the dyeing process, part of the dyes used to color textile materials are not fixed into the substrate and are discharged into wastewater as residual dyes. In this study, a heterogeneous photocatalytic process combined with microfiltration has been investigated for the removal of C.I. Disperse Red 73 from synthetic textile effluents. The titanium dioxide (TiO2 Aeroxide P25 was selected as photocatalyst. The photocatalytic treatment achieved between 60% and 90% of dye degradation and up to 98% chemical oxygen demand (COD removal. The influence of different parameters on photocatalytic degradation was studied: pH, initial photocatalyst loading, and dye concentration. The best conditions for dye degradation were pH 4, an initial dye concentration of 50 mg·L−1, and a TiO2 loading of 2 g·L−1. The photocatalytic membrane treatment provided a high quality permeate, which can be reused.

  18. Continuous Flow Science in an Undergraduate Teaching Laboratory: Photocatalytic Thiol-Ene Reaction Using Visible Light

    Science.gov (United States)

    Santandrea, Jeffrey; Kairouz, Vanessa; Collins, Shawn K.

    2018-01-01

    An undergraduate teaching laboratory experiment involving a continuous flow, photocatalytic thiol-ene reaction using visible-light irradiation is described that allows students to explore concepts of green chemistry, photochemistry, photocatalysis, and continuous flow chemistry.

  19. Efficient photocatalytic activity with carbon-doped SiO2 nanoparticles

    KAUST Repository

    Zhang, Dongen; Wu, Jinbo; Zhou, Bingpu; Hong, Yaying; Li, Shunbo; Wen, Weijia

    2013-01-01

    by thermogravimetric analysis, X-ray diffraction, standard and high resolution transmission electron microscopy and X-ray photoelectron spectroscopy. The C-doped SiO2 displayed outstanding photocatalytic properties, as evidenced by its catalysis of Rhodamine B

  20. Metal-free hybrids of graphitic carbon nitride and nanodiamonds for photoelectrochemical and photocatalytic applications.

    Science.gov (United States)

    Zhou, Li; Zhang, Huayang; Guo, Xiaochen; Sun, Hongqi; Liu, Shaomin; Tade, Moses O; Wang, Shaobin

    2017-05-01

    Graphitic carbon nitride (g-C 3 N 4 ) has been considered as a metal-free, cost-effective, eco-friendly and efficient catalyst for various photoelectrochemical applications. However, compared to conventional metal-based photocatalysts, its photocatalytic activity is still low because of the low mobility of carriers restricted by the polymer nature. Herein, a series of hybrids of g-C 3 N 4 (GCN) and nanodiamonds (NDs) were synthesized using a solvothermal method. The photoelectrochemical performance and photocatalytic efficiency of the GCN/NDs were investigated by means of the generation of photocurrent and photodegradation of methylene blue (MB) solutions under UV-visible light irradiations. In this study, the sample of GCN/ND-33% derived from 0.1g GCN and 0.05g NDs displayed the highest photocatalytic activity and the strongest photocurrent density. The mechanism of enhanced photoelectrochemical and photocatalytic performances was also discussed. Copyright © 2017 Elsevier Inc. All rights reserved.

  1. Photocatalytic hydrogen generation with Ag-loaded LiNbO3

    Indian Academy of Sciences (India)

    Administrator

    rhodamine B decomposition under solar illumination was also reported (Stock ... photocatalytic hydrogen production. ... lytic hydrogen production from a methanol aqueous solu- .... estimated bandgap energy of Nb2O5 and LiNbO3 samples.

  2. Facile Synthesis of Au Nanocube-CdS Core-Shell Nanocomposites with Enhanced Photocatalytic Activity

    Science.gov (United States)

    Liu, Xiao-Li; Liang, Shan; Li, Min; Yu, Xue-Feng; Zhou, Li; Wang, Qu-Qua

    2014-06-01

    Au nanocube-CdS core-shell nanocomposites are prepared by using a one-pot method in aqueous phase with cetyltrimethylammonium bromide as the surfactant. The extinction properties and photocatalytic activity of Au-CdS nanocomposites are investigated. Compared with the pure Au nanocubes, the Au-CdS nanocomposites exhibit enhanced extinction intensity. Compared with CdS nanoparticles, the Au-CdS nanocomposites exhibit improved photocatalytic activity. Furthermore, the photocatalytic efficiency is even better with the increase in the core size of the Au-CdS nanocomposites. Typically, the photocatalytic efficiency of the Au-CdS with 62 nm sized Au nanocubes is about two times higher than that of the pure CdS. It is believed that the Au-CdS nanocomposites may find potential applications in environmental fields, and this synthesis method can be extended to prepare a wide variety of functional composites with Au cores.

  3. Heterogeneous photocatalytic degradation of p-toluenesulfonic acid using concentrated solar radiation in slurry photoreactor

    International Nuclear Information System (INIS)

    Kamble, Sanjay P.; Sawant, Sudhir B.; Pangarkar, Vishwas G.

    2007-01-01

    In this work, the photocatalytic degradation (PCD) of p-toluenesulfonic acid (p-TSA) in batch reactor using concentrated solar radiation was investigated. The effect of the various operating parameters such as initial concentration of substrate, catalyst loading, solution pH and types of ions on photocatalytic degradation has been studied in a batch reactor to derive the optimum conditions. The rate of photocatalytic degradation was found to be maximum at the self pH (pH 3.34) of p-TSA. It was also observed that in the presence of anions and cations, the rate of PCD decreases drastically. The kinetics of photocatalytic degradation of p-TSA was studied. The PCD of p-TSA was also carried at these optimized conditions in a bench scale slurry bubble column reactor using concentrated solar radiation

  4. Next Generation Hybrid Photo-Catalytic Oxidation (PCO) for Trace Contaminant Control

    Data.gov (United States)

    National Aeronautics and Space Administration — Photocatalytic oxidation (PCO) is a primary candidate as an alternative to thermal-catalytic or sorbent- based technologies for VOC trace contaminant control due to...

  5. Experimental research on photocatalytic oxidation air purification technology applied to aircraft cabins

    DEFF Research Database (Denmark)

    Sun, Yuexia; Fang, Lei; Wyon, David Peter

    2008-01-01

    The experiment presented in this report was performed in a simulated aircraft cabin to evaluate the air cleaning effects of two air purification devices that used photocatalytic oxidation (PCO) technology. Objective physical, chemical and physiological measurements and subjective human assessment...

  6. Influence of ZnO concentration on the optical and photocatalytic ...

    Indian Academy of Sciences (India)

    Department of Applied Chemistry, University of Johannesburg, P.O. Box 17011, 2028 ... used to degrade the dye on the basis of influence of factors such as solution temperature, .... The photocatalytic degradation potential of the synthesized.

  7. Temperature dependence of electrocatalytic and photocatalytic oxygen evolution reaction rates using NiFe oxide

    KAUST Repository

    Nurlaela, Ela; Shinagawa, Tatsuya; Qureshi, Muhammad; Dhawale, Dattatray Sadashiv; Takanabe, Kazuhiro

    2016-01-01

    The present work compares oxygen evolution reaction (OER) in electrocatalysis and photocatalysis in aqueous solutions using nanostructured NiFeOx as catalysts. The impacts of pH and reaction temperature on the electrocatalytic and photocatalytic OER

  8. Photocatalytic decolorization of methylene blue over Zn1-xCoxO under visible light irradiation

    International Nuclear Information System (INIS)

    Xiao Qi; Zhang Jiang; Xiao Chong; Tan Xiaoke

    2007-01-01

    Co-doped ZnO photocatalysts were prepared by hydrothermal method. The obtained Co-doped ZnO powders were characterized by X-ray diffraction, UV-vis diffuse reflectance spectroscopy and photoluminescence (PL) spectra. The prepared Co-doped ZnO photocatalysts showed high photocatalytic activities for methylene blue decolorization at pH 10.5 under visible light irradiation. It was found that there were certain relationships between PL spectra and photocatalytic activity, namely, the stronger the PL intensity, the larger the content of oxygen vacancies and defects, the higher the photocatalytic activity. Therefore, in this study 3.0 mol% was the most suitable content of Co 2+ in ZnO, at which the recombination of photoinduced electrons and holes could be effectively inhibited and thereby the highest photocatalytic activity was formed

  9. Photocatalytic and Magnetic Behaviors Observed in BiFeO3 Nanofibers by Electrospinning

    Directory of Open Access Journals (Sweden)

    Xuehui Zhang

    2013-01-01

    Full Text Available Perovskite-type BiFeO3 nanofibers with wave nodes-like morphology were prepared by electrospinning. The nanofibers show a highly enhanced visible-light-active photocatalytic property. The results also showed that the diameter could affect the band gap and photocatalytic performances of nanofibers. Additionally, weak ferromagnetic behaviors can be observed at room temperature, which should be correlated to the size-confinement effect on the magnetic ordering of BiFeO3 structure.

  10. UV Blocking Glass: Low Cost Filters for Visible Light Photocatalytic Assessment

    OpenAIRE

    Dunnill, Charles W.

    2014-01-01

    A number of commercially available art protection products have been compared and assessed for their suitability as UV blocking filters in the application of “visible light” photocatalytic research. Many groups claiming visible light photocatalytic success employ filters to block out stray UV radiation in order to justify that their photocatalysts are indeed visible light photocatalysts and not UV light photocatalysts. These filters come in varying degrees of ability and price and many author...

  11. Treatment of wastewater dyeing agent by photocatalytic process in solar reactor

    OpenAIRE

    Zahraa, O.; Maire, S.; Evenou, F.; Hachem, C.; Pons, M. N.; Alinsafi, A.; Bouchy, M.

    2006-01-01

    The photocatalytic decolorization of industrial textile dyes has been studied. The treatment was carried out on a solar reactor consisting in a flat active plane, tilted so as to face the sun and to allow the trickling of the water to be treated. Alternatively the reactor could be irradiated by an artificial source. After checking the system using salicylic acid, a conventional model molecule, the photocatalytic decolorization of Orange II, Yellow Drimarene, and Black Drimarene dyes was inves...

  12. Solvent-free, visible-light photocatalytic alcohol oxidations applying an organic photocatalyst

    Directory of Open Access Journals (Sweden)

    Martin Obst

    2016-11-01

    Full Text Available A method for the solvent-free photocatalytic conversion of solid and liquid substrates was developed, using a novel rod mill apparatus. In this setup, thin liquid films are realized which is crucial for an effective photocatalytic conversion due to the low penetration depth of light in heterogeneous systems. Several benzylic alcohols were oxidized with riboflavin tetraacetate as photocatalyst under blue light irradiation of the reaction mixture. The corresponding carbonyl compounds were obtained in moderate to good yields.

  13. Synthesis of hierarchical anatase TiO 2 nanostructures with tunable morphology and enhanced photocatalytic activity

    KAUST Repository

    Rahal, Raed; Wankhade, Atul V.; Cha, Dong Kyu; Fihri, Aziz; Ould-Chikh, Samy; Patil, Umesh; Polshettiwar, Vivek

    2012-01-01

    A facile one-pot method to prepare three-dimensional hierarchical nanostructures of titania with good control over their morphologies without the use of hydrofluoric acid is developed. The reaction is performed under microwave irradiation conditions in pure water, and enables enhanced photocatalytic activity. This study indicates that photocatalytic activity depends not only on the surface area but also on the morphology of the titania. © 2012 The Royal Society of Chemistry.

  14. Substrate-Coated Illumination Droplet Spray Ionization: Real-Time Monitoring of Photocatalytic Reactions

    Science.gov (United States)

    Zhang, Hong; Li, Na; Zhao, Dandan; Jiang, Jie; You, Hong

    2017-09-01

    Real-time monitoring of photocatalytic reactions facilitates the elucidation of the mechanisms of the reactions. However, suitable tools for real-time monitoring are lacking. Herein, a novel method based on droplet spray ionization named substrate-coated illumination droplet spray ionization (SCI-DSI) for direct analysis of photocatalytic reaction solution is reported. SCI-DSI addresses many of the analytical limitations of electrospray ionization (ESI) for analysis of photocatalytic-reaction intermediates, and has potential for both in situ analysis and real-time monitoring of photocatalytic reactions. In SCI-DSI-mass spectrometry (MS), a photocatalytic reaction occurs by loading sample solutions onto the substrate-coated cover slip and by applying UV light above the modified slip; one corner of this slip adjacent to the inlet of a mass spectrometer is the high-electric-field location for launching a charged-droplet spray. After both testing and optimizing the performance of SCI-DSI, the value of this method for in situ analysis and real-time monitoring of photocatalytic reactions was demonstrated by the removal of cyclophosphamide (CP) in TiO2/UV. Reaction times ranged from seconds to minutes, and the proposed reaction intermediates were captured and identified by tandem mass spectrometry. Moreover, the free hydroxyl radical (·OH) was identified as the main radicals for CP removal. These results show that SCI-DSI is suitable for in situ analysis and real-time monitoring of CP removal under TiO2-based photocatalytic reactions. SCI-DSI is also a potential tool for in situ analysis and real-time assessment of the roles of radicals during CP removal under TiO2-based photocatalytic reactions. Graphical Abstract[Figure not available: see fulltext.

  15. Photocatalytic degradation of diethyl phthalate using TiO{sub 2} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Singla, Pooja, E-mail: pooja.singla@thapar.edu; Pandey, O. P., E-mail: pooja.singla@thapar.edu; Singh, K., E-mail: pooja.singla@thapar.edu [School of Physics and Materials Science, Thapar University, Patiala-147004 (India)

    2014-04-24

    TiO{sub 2} nanoparticles predominantly in rutile phase are synthesized by ultrasonication assisted sol-gel method. TiO{sub 2} powder is characterized using X-ray powder diffraction and UV-vis diffuse reflectance. TiO{sub 2} is used as catalyst in photocatalytic degradation of Diethyl Phthalate. TiO{sub 2} exhibits good photocatalytic activity for the degradation of diethyl phthalate.

  16. Enhanced Photocatalytic Activity of La3+-Doped TiO2 Nanotubes with Full Wave-Band Absorption

    Science.gov (United States)

    Xia, Minghao; Huang, Lingling; Zhang, Yubo; Wang, Yongqian

    2018-06-01

    TiO2 nanotubes doped with La3+ were synthesized by anodic oxidation method and the photocatalytic activity was detected by photodegrading methylene blue. As-prepared samples improved the absorption of both ultraviolet light and visible light and have a great enhancement on the photocatalytic activity while contrasting with the pristine TiO2 nanotubes. A tentative mechanism for the enhancement of photocatalytic activity with full wave-band absorption is proposed.

  17. Photoluminescence and photocatalytic activities of Ag/ZnO metal-semiconductor heterostructure

    International Nuclear Information System (INIS)

    Sarma, Bikash; Deb, Sujit Kumar; Sarma, Bimal K.

    2016-01-01

    Present article focuses on the photocatalytic activities of ZnO nanorods and Ag/ZnO heterostructure deposited on polyethylene terephthalate (PET) substrate. ZnO nanorods are synthesized by thermal decomposition technique and Ag nanoparticles deposition is done by photo-deposition technique using UV light. X-ray diffraction studies reveal that the ZnO nanorods are of hexagonal wurtzite structure. Further, as-prepared samples are characterized by Scanning Electron Microscopy (SEM), Photoluminescence (PL) spectroscopy and UV-Vis spectroscopy. The surface plasmon resonance response of Ag/ZnO is found at 420 nm. The photocatalytic activities of the samples are evaluated by photocatalytic decolorization of methyl orange (MO) dye with UV irradiation. The degradation rate of MO increases with increase in irradiation time. The degradation of MO follows the first order kinetics. The photocatalytic activity of Ag/ZnO heterostructure is found to be more than that of ZnO nanorods. The PL intensity of ZnO nanorods is stronger than that of the Ag/ZnO heterostructure. The strong PL intensity indicates high recombination rate of photoinduced charge carriers which lowers the photocatalytic activity of ZnO nanorods. The charge carrier recombination is effectively suppressed by introducing Ag nanoparticles on the surface of the ZnO nanorods. This study demonstrates a strong relationship between PL intensity and photocatalytic activity. (paper)

  18. Graphene quantum dots /LaCoO3/attapulgite heterojunction photocatalysts with improved photocatalytic activity

    International Nuclear Information System (INIS)

    Zhu, Wei; Li, Xiazhang

    2017-01-01

    A new nanocomposite of graphene quantum dots/LaCoO 3 /attapulgite (GQDs/LaCoO 3 /ATP) was prepared by a facile impregnation method and was applied to degradation of the organic pollutants as photocatalyst under visible light irradiation. Multiple techniques were used to characterize the structures, morphologies and photocatalytic activities of samples. The photocatalytic activity of the GQDs/LaCoO 3 /ATP nanocomposites was effectively evaluated using Methylene blue (MB), antibiotic agent chlortetracycline (CHL) and tetracycline hydrochloride (TC). The as-synthesized GQDs/LaCoO 3 /ATP nanocomposites exhibited higher photocatalytic activities than LaCoO 3 /ATP, which showed a broad spectrum of photocatalytic degradation activity. The results of ESR and free radicals trapping experiments indicated that circle OH and h + were the main species for the photocatalytic degradation. GQDs played a significant role in the photocatalytic activity improvement of LaCoO 3 /ATP, increasing the visible light absorption, slowing the recombination and improving the charge transfer. (orig.)

  19. Graphene quantum dots /LaCoO3/attapulgite heterojunction photocatalysts with improved photocatalytic activity

    Science.gov (United States)

    Zhu, Wei; Li, Xiazhang

    2017-04-01

    A new nanocomposite of graphene quantum dots/LaCoO3/attapulgite (GQDs/LaCoO3/ATP) was prepared by a facile impregnation method and was applied to degradation of the organic pollutants as photocatalyst under visible light irradiation. Multiple techniques were used to characterize the structures, morphologies and photocatalytic activities of samples. The photocatalytic activity of the GQDs/LaCoO3/ATP nanocomposites was effectively evaluated using Methylene blue (MB), antibiotic agent chlortetracycline (CHL) and tetracycline hydrochloride (TC). The as-synthesized GQDs/LaCoO3/ATP nanocomposites exhibited higher photocatalytic activities than LaCoO3/ATP, which showed a broad spectrum of photocatalytic degradation activity. The results of ESR and free radicals trapping experiments indicated that • OH and h+ were the main species for the photocatalytic degradation. GQDs played a significant role in the photocatalytic activity improvement of LaCoO3/ATP, increasing the visible light absorption, slowing the recombination and improving the charge transfer.

  20. Synthesis and photocatalytic activity of poly(3-hexylthiophene)/TiO2 composites

    International Nuclear Information System (INIS)

    Muktha, B.; Mahanta, Debajyoti; Patil, Satish; Madras, Giridhar

    2007-01-01

    An heterogeneous conducting polymer composite, poly(3-hexylthiophene)/TiO 2 (P3HT/TiO 2 ), was synthesized. The photocatalytic activity of P3HT alone and the composite was investigated for the first time by degrading a common dye under UV exposure. It was shown that the photocatalytic activity of the nanocomposites was higher compared to either the polymer or TiO 2 alone. A simple mechanism was proposed to explain this observed synergetic effect. - Graphical abstract: Photocatalytic mechanism of the polymer composite with titania. A new heterogeneous conducting polymer composite with titania (P3HT/TiO 2 ) was synthesized and the photocatalytic activity this composite was investigated by degrading a common dye under UV exposure. It was shown that the nanocomposite exhibited synergetic photocatalytic catalytic activity compared to either the polymer or TiO 2 alone. The scheme of the possible mechanism of enhancement of photocatalytic degradation rate in a conducting polymer nanocomposite is shown in the figure

  1. CFD modeling of a UV-LED photocatalytic odor abatement process in a continuous reactor

    International Nuclear Information System (INIS)

    Wang, Zimeng; Liu, Jing; Dai, Yuancan; Dong, Weiyang; Zhang, Shicheng; Chen, Jianmin

    2012-01-01

    Highlights: ► A CFD model is developed for a UV-LED based photocatalytic deodorization reactor. ► Radiation field model and Langmuir–Hinshelwood kinetics are integrated in the model. ► The model can predict the pollutant concentration profile and the reactor performance. ► LED distance is predicted to be a critical parameter in photocatalytic reactor design. - Abstract: This paper presents a model study of a UV light-emitting-diode (UV-LED) based photocatalytic odor abatement process. It integrated computational fluid dynamics (CFD) modeling of the gas flow in the reactor with LED-array radiation field calculation and Langmuir–Hinshelwood reaction kinetics. It was applied to simulate the photocatalytic degradation of dimethyl sulfide (DMS) in a UV-LED reactor based on experimentally determined chemical kinetic parameters. A non-linear power law relating reaction rate to irradiation intensity was adopted. The model could predict the steady state DMS concentration profiles by calculating the advection, diffusion and Langmuir–Hinshelwood reaction kinetics. By affecting the radiation intensity and uniformity, the position of the LED array relative to the catalyst appeared to be a critical parameter determining DMS removal efficiency. Too small distances might yield low quantum efficiency and consequently poor abatement performance. This study provided an example of LED-based photocatalytic process modeling and gave insights into the optimization of light source design for photocatalytic applications.

  2. Nest-like structures of Sr doped Bi2WO6: Synthesis and enhanced photocatalytic properties

    International Nuclear Information System (INIS)

    Liu Ying; Wang Weimin; Fu Zhengyi; Wang Hao; Wang Yucheng; Zhang Jinyong

    2011-01-01

    Highlights: → Bi 2 WO 6 with 3D nest-like structures was obtained without the presence of templates but after Sr-doping, which represents a marked improvement over previous reports. → The products showed enhanced photocatalytic properties over pure Bi 2 WO 6 . → Samples subsequently thermal treated at 500 deg. C show better photocatalytic activities. - Abstract: A series of Sr-doped Bi 2 WO 6 with three-dimensional (3D) nest-like structures were synthesized through simple hydrothermal route and characterized by XRD, FESEM, TEM, XPS, UV-vis DRS, etc. Morphology observation revealed that the as-synthesized Bi 2 WO 6 were self-assembled three-dimensional (3D) nest-like structures, which were constructed from nanoplates. UV-vis diffuse reflectance spectra indicated that the samples had absorption in both UV and visible light areas. Their photocatalytic activities were evaluated by photodegradation of rhodamine B (RhB) under UV and visible light irradiation (λ > 420 nm). The photocatalytic properties were enhanced after Sr doping. Samples subsequently thermal treated at 500 deg. C showed higher photocatalytic activities. The reasons for the differences in the photocatalytic activities of these nest-like Bi 2 WO 6 microstructures were further investigated.

  3. Enhanced visible light photocatalytic property of red phosphorus via surface roughening

    International Nuclear Information System (INIS)

    Li, Weibing; Yue, Jiguang; Hua, Fangxia; Feng, Chang; Bu, Yuyu; Chen, Zhuoyuan

    2015-01-01

    Highlights: • Photocatalytic RhB degradation of red phosphorus was studied for the first time. • Surface rough can increase the photocatalysis reaction active sites. • Surface rough red phosphorus possesses high photocatalytic performance. • Surface rough red phosphorus has high industrial application value. - Abstract: Red phosphorus with rough surface (SRP) was prepared by catalyst-assisted hydrothermal synthesis using Co 2+ catalyst. The photocatalytic Rhodamine B (RhB) degradation of red phosphorus (RP) and SRP was studied for the first time in this work. Rough surface can enhance the dye adsorption ability of RP. About 75% RhB was absorbed by SRP after 30-min adsorption in 100 ml RhB solution with concentration of 10 mg l −1 in dark. After only 10 min of illumination by visible light, more than 95% RhB was degraded, indicating that SRP has a great application potential in the area of photocatalysis. The photocatalytic RhB degradation properties of RP are much weaker than those of SRP. The increase of the number of the active sites for the photocatalytic reactions, the electron mobility and the lifetime of the photogenerated electrons cause the significant improvement of the photocatalytic performance of SRP based on the experimental results obtained

  4. A transparent Pyrex μ-reactor for combined in situ optical characterization and photocatalytic reactivity measurements

    International Nuclear Information System (INIS)

    Dionigi, F.; Hansen, O.; Nielsen, M. G.; Chorkendorff, I.; Vesborg, P. C. K.; Pedersen, T.

    2013-01-01

    A new Pyrex-based μ-reactor for photocatalytic and optical characterization experiments is presented. The reactor chamber and gas channels are microfabricated in a thin poly-silicon coated Pyrex chip that is sealed with a Pyrex lid by anodic bonding. The device is transparent to light in the UV-vis-near infrared range of wavelengths (photon energies between ∼0.4 and ∼4.1 eV). The absorbance of a photocatalytic film obtained with a light transmission measurement during a photocatalytic reaction is presented as a proof of concept of a photocatalytic reactivity measurement combined with in situ optical characterization. Diffuse reflectance measurements of highly scattering photocatalytic nanopowders in a sealed Pyrex μ-reactor are also possible using an integrating sphere as shown in this work. These experiments prove that a photocatalyst can be characterized with optical techniques after a photocatalytic reaction without removing the material from the reactor. The catalyst deposited in the cylindrical reactor chamber can be illuminated from both top and bottom sides and an example of application of top and bottom illumination is presented

  5. Effects of electromechanical resonance on photocatalytic reduction of the free-hanging graphene oxide sheets

    International Nuclear Information System (INIS)

    Ostovari, F.; Abdi, Y.; Darbari, S.; Ghasemi, F.

    2013-01-01

    In this report we present a simple, low-temperature method which is compatible with standard technology, to achieve graphene-based devices in large quantity. In this approach we take advantage of photocatalytic behavior of TiO 2 to achieve photocatalytic reduction of chemically synthesized graphene oxide (GO) sheets. TiO 2 nanoparticles have been deposited on GO sheets hanging from Au/SiO 2 /Si interdigital electrodes to realize TiO 2 /GO heterostructures. We investigated photocatalytic activity of TiO 2 nanoparticles in the presence of UV-illumination, to reduce the GO sheets. Based on the Raman spectroscopy, the photocatalytic activity of TiO 2 nanoparticles resulted in a decrease in the number of C–O bonds. Electrical measurements show that graphene sheets with the controlled electrical conductivity were obtained, so that higher illumination time led to higher conductivity and better reduction of GO sheets. Also, strain-induced photocatalytic reduction of the GO sheets has been investigated by their electrical characteristics. It has been shown for the first time that the electromechanical-induced strain enhances the photocatalytic behavior of the fabricated TiO 2 /GO heterostructure significantly.

  6. Effects of electromechanical resonance on photocatalytic reduction of the free-hanging graphene oxide sheets

    Energy Technology Data Exchange (ETDEWEB)

    Ostovari, F.; Abdi, Y., E-mail: y.abdi@ut.ac.ir [University of Tehran, Nano-Physics Research Laboratory, Department of Physics (Iran, Islamic Republic of); Darbari, S. [Tarbiat Modarres University (Iran, Islamic Republic of); Ghasemi, F. [University of Tehran, Nano-Physics Research Laboratory, Department of Physics (Iran, Islamic Republic of)

    2013-04-15

    In this report we present a simple, low-temperature method which is compatible with standard technology, to achieve graphene-based devices in large quantity. In this approach we take advantage of photocatalytic behavior of TiO{sub 2} to achieve photocatalytic reduction of chemically synthesized graphene oxide (GO) sheets. TiO{sub 2} nanoparticles have been deposited on GO sheets hanging from Au/SiO{sub 2}/Si interdigital electrodes to realize TiO{sub 2}/GO heterostructures. We investigated photocatalytic activity of TiO{sub 2} nanoparticles in the presence of UV-illumination, to reduce the GO sheets. Based on the Raman spectroscopy, the photocatalytic activity of TiO{sub 2} nanoparticles resulted in a decrease in the number of C-O bonds. Electrical measurements show that graphene sheets with the controlled electrical conductivity were obtained, so that higher illumination time led to higher conductivity and better reduction of GO sheets. Also, strain-induced photocatalytic reduction of the GO sheets has been investigated by their electrical characteristics. It has been shown for the first time that the electromechanical-induced strain enhances the photocatalytic behavior of the fabricated TiO{sub 2}/GO heterostructure significantly.

  7. Enhanced visible light photocatalytic property of red phosphorus via surface roughening

    Energy Technology Data Exchange (ETDEWEB)

    Li, Weibing, E-mail: lwbing@qust.edu.cn [School of Environment and Safety Engineering, Qingdao University of Science and Technology, 53 Zhengzhou Road, Qingdao 266042 (China); Yue, Jiguang; Hua, Fangxia; Feng, Chang [School of Environment and Safety Engineering, Qingdao University of Science and Technology, 53 Zhengzhou Road, Qingdao 266042 (China); Bu, Yuyu; Chen, Zhuoyuan [Key Laboratory of Marine Environmental Corrosion and Bio-fouling, Institute of Oceanology, Chinese Academy of Sciences, 7 Nanhai Road, Qingdao 266071 (China)

    2015-10-15

    Highlights: • Photocatalytic RhB degradation of red phosphorus was studied for the first time. • Surface rough can increase the photocatalysis reaction active sites. • Surface rough red phosphorus possesses high photocatalytic performance. • Surface rough red phosphorus has high industrial application value. - Abstract: Red phosphorus with rough surface (SRP) was prepared by catalyst-assisted hydrothermal synthesis using Co{sup 2+} catalyst. The photocatalytic Rhodamine B (RhB) degradation of red phosphorus (RP) and SRP was studied for the first time in this work. Rough surface can enhance the dye adsorption ability of RP. About 75% RhB was absorbed by SRP after 30-min adsorption in 100 ml RhB solution with concentration of 10 mg l{sup −1} in dark. After only 10 min of illumination by visible light, more than 95% RhB was degraded, indicating that SRP has a great application potential in the area of photocatalysis. The photocatalytic RhB degradation properties of RP are much weaker than those of SRP. The increase of the number of the active sites for the photocatalytic reactions, the electron mobility and the lifetime of the photogenerated electrons cause the significant improvement of the photocatalytic performance of SRP based on the experimental results obtained.

  8. Graphene quantum dots /LaCoO{sub 3}/attapulgite heterojunction photocatalysts with improved photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Wei; Li, Xiazhang [Changzhou University, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou (China); Chinese Academy of Science, R and D Center of Xuyi Attapulgite Applied Technology, Xuyi (China)

    2017-04-15

    A new nanocomposite of graphene quantum dots/LaCoO{sub 3}/attapulgite (GQDs/LaCoO{sub 3}/ATP) was prepared by a facile impregnation method and was applied to degradation of the organic pollutants as photocatalyst under visible light irradiation. Multiple techniques were used to characterize the structures, morphologies and photocatalytic activities of samples. The photocatalytic activity of the GQDs/LaCoO{sub 3}/ATP nanocomposites was effectively evaluated using Methylene blue (MB), antibiotic agent chlortetracycline (CHL) and tetracycline hydrochloride (TC). The as-synthesized GQDs/LaCoO{sub 3}/ATP nanocomposites exhibited higher photocatalytic activities than LaCoO{sub 3}/ATP, which showed a broad spectrum of photocatalytic degradation activity. The results of ESR and free radicals trapping experiments indicated that {sup circle} OH and h {sup +} were the main species for the photocatalytic degradation. GQDs played a significant role in the photocatalytic activity improvement of LaCoO{sub 3}/ATP, increasing the visible light absorption, slowing the recombination and improving the charge transfer. (orig.)

  9. Controlled Defects of Zinc Oxide Nanorods for Efficient Visible Light Photocatalytic Degradation of Phenol

    Directory of Open Access Journals (Sweden)

    Jamal Al-Sabahi

    2016-03-01

    Full Text Available Environmental pollution from human and industrial activities has received much attention as it adversely affects human health and bio-diversity. In this work we report efficient visible light photocatalytic degradation of phenol using supported zinc oxide (ZnO nanorods and explore the role of surface defects in ZnO on the visible light photocatalytic activity. ZnO nanorods were synthesized on glass substrates using a microwave-assisted hydrothermal process, while the surface defect states were controlled by annealing the nanorods at various temperatures and were characterized by photoluminescence and X-ray photoelectron spectroscopy. High performance liquid chromatography (HPLC was used for the evaluation of phenol photocatalytic degradation. ZnO nanorods with high surface defects exhibited maximum visible light photocatalytic activity, showing 50% degradation of 10 ppm phenol aqueous solution within 2.5 h, with a degradation rate almost four times higher than that of nanorods with lower surface defects. The mineralization process of phenol during degradation was also investigated, and it showed the evolution of different photocatalytic byproducts, such as benzoquinone, catechol, resorcinol and carboxylic acids, at different stages. The results from this study suggest that the presence of surface defects in ZnO nanorods is crucial for its efficient visible light photocatalytic activity, which is otherwise only active in the ultraviolet region.

  10. Biological and photocatalytic treatment integrated with separation and reuse of titanium dioxide on the removal of chlorophenols in tap water

    International Nuclear Information System (INIS)

    Suryaman, Dhanus; Hasegawa, Kiyoshi

    2010-01-01

    We investigated biological, photocatalytic, and combination of biological and photocatalytic treatments in order to remove a mixture of 2-chlorophenol, 2,4-dichlorophenol, 2,4,5-trichlorophenol, and pentachlorophenol in tap water (total: 100 mg L -1 , each: 25 mg L -1 ). The removal of chlorinated phenols was conducted with a flow biological treatment and a circulative flow photocatalytic treatment under black light and sunlight irradiations integrated with titanium dioxide separation and reuse. The combined biological-photocatalytic treatment significantly shortened the degradation and mineralization time of both the biological treatment and the photocatalytic treatment. The removed chlorophenols per hour by the combined biological-photocatalytic treatment was 25.8 mg h -1 , whereas by the combined photocatalytic-biological treatment was 10.5 mg h -1 . After a large portion of biodegradable 2-chlorophenol and 2,4-dichlorophenol, and around half amount of slightly biodegradable 2,4,5-trichlorophenol were removed by the biological treatment, the remained three chlorophenols, biorecalcitrant pentachlorophenol, and biodegradation products were completely removed by the subsequent photocatalytic treatment. Since titanium dioxide particles in tap water spontaneously sedimented on standing after the photocatalytic treatment, the combined treatment can be operated by integrating with the titanium dioxide separation and reuse. The TiO 2 particles were recovered and reused at least three times without significantly decreasing the removal efficiency.

  11. Biological and photocatalytic treatment integrated with separation and reuse of titanium dioxide on the removal of chlorophenols in tap water

    Energy Technology Data Exchange (ETDEWEB)

    Suryaman, Dhanus, E-mail: dhanussuryaman@yahoo.com [Agency for the Assessment and Application of Technology, M.H. Thamrin No. 8, Jakarta 10340 (Indonesia); Department of Chemical and Biochemical Engineering, Faculty of Engineering, University of Toyama, 3190 Gofuku, Toyama 930-8555 (Japan); Hasegawa, Kiyoshi [Department of Chemical and Biochemical Engineering, Faculty of Engineering, University of Toyama, 3190 Gofuku, Toyama 930-8555 (Japan)

    2010-11-15

    We investigated biological, photocatalytic, and combination of biological and photocatalytic treatments in order to remove a mixture of 2-chlorophenol, 2,4-dichlorophenol, 2,4,5-trichlorophenol, and pentachlorophenol in tap water (total: 100 mg L{sup -1}, each: 25 mg L{sup -1}). The removal of chlorinated phenols was conducted with a flow biological treatment and a circulative flow photocatalytic treatment under black light and sunlight irradiations integrated with titanium dioxide separation and reuse. The combined biological-photocatalytic treatment significantly shortened the degradation and mineralization time of both the biological treatment and the photocatalytic treatment. The removed chlorophenols per hour by the combined biological-photocatalytic treatment was 25.8 mg h{sup -1}, whereas by the combined photocatalytic-biological treatment was 10.5 mg h{sup -1}. After a large portion of biodegradable 2-chlorophenol and 2,4-dichlorophenol, and around half amount of slightly biodegradable 2,4,5-trichlorophenol were removed by the biological treatment, the remained three chlorophenols, biorecalcitrant pentachlorophenol, and biodegradation products were completely removed by the subsequent photocatalytic treatment. Since titanium dioxide particles in tap water spontaneously sedimented on standing after the photocatalytic treatment, the combined treatment can be operated by integrating with the titanium dioxide separation and reuse. The TiO{sub 2} particles were recovered and reused at least three times without significantly decreasing the removal efficiency.

  12. Fuel rods

    International Nuclear Information System (INIS)

    Adachi, Hajime; Ueda, Makoto

    1985-01-01

    Purpose: To provide a structure capable of measuring, in a non-destructive manner, the releasing amount of nuclear gaseous fission products from spent fuels easily and at a high accuracy. Constitution: In order to confirm the integrity and the design feasibility of a nuclear fuel rod, it is important to accurately determine the amount of gaseous nuclear fission products released from nuclear pellets. In a structure where a plurality of fuel pellets are charged in a fuel cladding tube and retained by an inconel spring, a hollow and no-sealed type spacer tube made of zirconium or the alloy thereof, for example, not containing iron, cobalt, nickel or manganese is formed between the spring and the upper end plug. In the fuel rod of such a structure, by disposing a gamma ray collimator and a gamma ray detector on the extension of the spacer pipe, the gamma rays from the gaseous nuclear fission products accumulated in the spacer pipe can be detected while avoiding the interference with the induction radioactivity from inconel. (Kamimura, M.)

  13. Fuel rods

    International Nuclear Information System (INIS)

    Hattori, Shinji; Kajiwara, Koichi.

    1980-01-01

    Purpose: To ensure the safety for the fuel rod failures by adapting plenum springs to function when small forces such as during transportation of fuel rods is exerted and not to function the resilient force when a relatively great force is exerted. Constitution: Between an upper end plug and a plenum spring in a fuel rod, is disposed an insertion member to the lower portion of which is mounted a pin. This pin is kept upright and causes the plenum spring to function resiliently to the pellets against the loads due to accelerations and mechanical vibrations exerted during transportation of the fuel rods. While on the other hand, if a compression force of a relatively high level is exerted to the plenum spring during reactor operation, the pin of the insertion member is buckled and the insertion member is inserted to the inside of the plenum spring, whereby the pellets are allowed to expand freely and the failures in the fuel elements can be prevented. (Moriyama, K.)

  14. Fuel assembly

    International Nuclear Information System (INIS)

    Abe, Hideaki; Sakai, Takao; Ishida, Tomio; Yokota, Norikatsu.

    1992-01-01

    The lower ends of a plurality of plate-like shape memory alloys are secured at the periphery of the upper inside of the handling head of a fuel assembly. As the shape memory alloy, a Cu-Zn alloy, a Ti-Pd alloy or a Fe-Ni alloy is used. When high temperature coolants flow out to the handling head, the shape memory alloy deforms by warping to the outer side more greatly toward the upper portion thereof with the temperature increase of the coolants. As the result, the shape of the flow channel of the coolants is changed so as to enlarge at the exit of the upper end of the fuel assembly. Then, the pressure loss of the coolants in the fuel assembly is decreased by the enlargement. Accordingly, the flow rate of the coolants in the fuel assembly is increased to lower the temperature of the coolants. Further, high temperature coolants and low temperature coolants are mixed sufficiently just above the fuel assembly. This can suppress the temperature fluctuation of the mixed coolants in the upper portion of the reactor core, thereby enabling to decrease a fatigue and failures of the structural components in the upper portion of the reactor core. (I.N.)

  15. Fuel assembly

    International Nuclear Information System (INIS)

    Sano, Hiroki; Fushimi, Atsushi; Tominaga, Kenji; Aoyama, Motoo; Ishii, Kazuya.

    1997-01-01

    In burnable poison-incorporated uranium fuels of a BWR type reactor, the compositional ratio of isotopes of the burnable poisons is changed so as to increase the amount of those having a large neutron absorbing cross sectional area. For example, if the ratio of Gd-157 at the same burnable poison enrichment degree is made greater than the natural ratio, this gives the same effect as the increase of the enrichment degree per one fuel rod, thereby providing an effect of reducing a surplus reactivity. Gadolinium, hafnium and europium as burnable poisons have an absorbing cross sectional area being greater in odd numbered nuclei than in even numbered nuclei, on the contrary, boron has a cross section being greater in even numbered nucleus than odd numbered nuclei. Accordingly, if the ratio of isotopes having greater cross section at the same burnable poison enrichment degree is made greater than the natural ratio, surplus reactivity at the initial stage of the burning can be reduced without greatly increasing the amount of burnable poison-incorporated uranium fuels, fuel loading amount is not reduced and the fuel economy is not worsened. (N.H.)

  16. Canadian power reactor fuel

    International Nuclear Information System (INIS)

    Page, R.D.

    1976-03-01

    The following subjects are covered: the basic CANDU fuel design, the history of the bundle design, the significant differences between CANDU and LWR fuel, bundle manufacture, fissile and structural materials and coolants used in the CANDU fuel program, fuel and material behaviour, and performance under irradiation, fuel physics and management, booster rods and reactivity mechanisms, fuel procurement, organization and industry, and fuel costs. (author)

  17. Photonic Nanoparticle Doped Architectures for Enhanced Solar to Fuel Photocatalytic Conversion 154060

    Science.gov (United States)

    2016-12-09

    redispersed in 15 mL of DI water using ultrasonic vibration . Zinc nitrate hexahydrate (0.3 mmol), indium(III) nitrate hydrate (0.6 mmol), and...2016, May). Keynote Speaker : Research First Look Symposium; Houston, Texas. • T. R. Lee (2016, May). Invited talk: University of California at

  18. Multimetallic Systems for the Photocatalytic Production of Fuels from Abundant Sources

    Energy Technology Data Exchange (ETDEWEB)

    Dunbar, Kim; Turro, Claudia [The Ohio State University

    2018-04-01

    The reported findings herein are a result of a collaboration between the groups of Claudia Turro at The Ohio State University (DE-SC0010542) and Kim R. Dunbar at Texas A&M University (DE-SC0010721). The Turro and Dunbar groups jointly discovered that cationic d7–d7 Rh2(II,II) complexes bridged by electron-donating formamidinate (form) ligands possess redox-active excited states that are relatively long-lived and can engage in charge transfer reactions. As part of the present grant we designed new complexes that exhibit strong absorption from the UV to ~800 nm. The Rh2(II,II) complexes under investigation are poised to undergo catalytic reduction of substrates because they are robust to changes in metal oxidation state, the two metals and the two diimine ligands, together with the non-innocent bridges, can be used to store redox equivalents, making these complexes capable of coupling one-electron events with multi-electron transformations. We discovered the electrocatalytic reduction of H+ and CO2 by complexes that are able to electrocatalytically reduce H+ to H2 with high turnover frequencies (TOFs) and overpotentials, η, of ~0.5 V,8 as well as to reduce CO2 to HCOOH. We now have experimental evidence that both the production of H2 from H+ and HCOOH. The molecular catalysts are stable after the acid and/or CO2 is consumed since electrocatalysis is restored at the same rate upon the addition of substrate to the cell.8,9 Moreover, we showed that the catalysis is not a result of a decomposition product deposited on the electrode, since placing an electrode from an active electrocatalytic solution into one that does not contain catalyst completely shuts down the reactivity. We are currently exploring the reactivity of these complexes in hydride transfer reactions with other substrates and in the presence of CO2 and reducing agents, as well as attempting to grow single crystals for x-ray diffraction.

  19. Core-Shell Photonic Nanoparticles for Enhanced Solar-to-Fuel Photocatalytic Conversion

    Science.gov (United States)

    2017-10-11

    ncu.edu.tw; National Central University; Department of Chemical and Materials Engineering; 300 Jhongda Road, Jhongli District, Taoyuan County, Taiwan...nanoparticles as photocatalysts in the water-splitting reaction . The second thrust focused on tuning the dielectric environment of GS-NS nanoparticles by...SnO2, a method that should allow modulating the band gap of the semiconducting material. Additionally, we explored the synthesis and optical

  20. Carbon-doped SnS2 nanostructure as a high-efficiency solar fuel catalyst under visible light.

    Science.gov (United States)

    Shown, Indrajit; Samireddi, Satyanarayana; Chang, Yu-Chung; Putikam, Raghunath; Chang, Po-Han; Sabbah, Amr; Fu, Fang-Yu; Chen, Wei-Fu; Wu, Chih-I; Yu, Tsyr-Yan; Chung, Po-Wen; Lin, M C; Chen, Li-Chyong; Chen, Kuei-Hsien

    2018-01-12

    Photocatalytic formation of hydrocarbons using solar energy via artificial photosynthesis is a highly desirable renewable-energy source for replacing conventional fossil fuels. Using an L-cysteine-based hydrothermal process, here we synthesize a carbon-doped SnS 2 (SnS 2 -C) metal dichalcogenide nanostructure, which exhibits a highly active and selective photocatalytic conversion of CO 2 to hydrocarbons under visible-light. The interstitial carbon doping induced microstrain in the SnS 2 lattice, resulting in different photophysical properties as compared with undoped SnS 2 . This SnS 2 -C photocatalyst significantly enhances the CO 2 reduction activity under visible light, attaining a photochemical quantum efficiency of above 0.7%. The SnS 2 -C photocatalyst represents an important contribution towards high quantum efficiency artificial photosynthesis based on gas phase photocatalytic CO 2 reduction under visible light, where the in situ carbon-doped SnS 2 nanostructure improves the stability and the light harvesting and charge separation efficiency, and significantly enhances the photocatalytic activity.

  1. CANDU fuel

    International Nuclear Information System (INIS)

    MacEwan, J.R.; Notley, M.J.F.; Wood, J.C.; Gacesa, M.

    1982-09-01

    The direction of CANDU fuel development was set in 1957 with the decision to build pressure tube reactors. Short - 50 cm long - rodded bundles of natural UO 2 clad in Zircaloy were adopted to facilitate on-power fuelling to improve uranium utilization. Progressive improvements were made during 25 years of development, involving 650 man years and 180 million dollars. Today's CANDU bundle is based on the knowledge gained from extensive irradiation testing and experience in power reactors. The main thrust of future development is to demonstrate that the present bundle is suitable, with minor modifications, for thorium fuels

  2. Novel Photocatalytic Reactor Development for Removal of Hydrocarbons from Water

    Directory of Open Access Journals (Sweden)

    Morgan Adams

    2008-01-01

    Full Text Available Hydrocarbons contamination of the marine environment generated by the offshore oil and gas industry is generated from a number of sources including oil contaminated drill cuttings and produced waters. The removal of hydrocarbons from both these sources is one of the most significant challenges facing this sector as it moves towards zero emissions. The application of a number of techniques which have been used to successfully destroy hydrocarbons in produced water and waste water effluents has previously been reported. This paper reports the application of semiconductor photocatalysis as a final polishing step for the removal of hydrocarbons from two waste effluent sources. Two reactor concepts were considered: a simple flat plate immobilised film unit, and a new rotating drum photocatalytic reactor. Both units proved to be effective in removing residual hydrocarbons from the effluent with the drum reactor reducing the hydrocarbon content by 90% under 10 minutes.

  3. Power-dependent photocatalytic activity of ZnO

    Energy Technology Data Exchange (ETDEWEB)

    Chun, So Yeon; Han, Noh Soo; Jeong, Seong Hyun; Park, Seung Min; Song, Jae Kyu [Dept. of Chemistry, Kyung Hee University, Seoul (Korea, Republic of); Moon, Cheol Joo; Choi, Myong Yong [Dept. of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang NationalUniversity, Jinju (Korea, Republic of)

    2017-03-15

    the power-dependent photocatalytic activity of ZnO was examined for the photoreduction processes of Rh101 and AN in the presence of hole scavengers, where the fluorescence spectra were measured as a function of irradiation time and excitation intensity. The concentration of the reactants decreased, while the concentration of the products increased accordingly, which indicated the single-electron reduction process by electrons supplied from the conduction band of ZnO. Despite the single-electron process, the efficiency of the photoreaction depended nonlinearly on the excitation intensity, which was explained by the saturation of defect states in ZnO. The enhanced ratio of available electrons in ZnO led to a superlinear increase in the photoreduction efficiency, while the single-electron process linearly reflected the electrons available in ZnO.

  4. Bioinspired nanocoatings for biofouling prevention by photocatalytic redox reactions.

    Science.gov (United States)

    Sathe, Priyanka; Laxman, Karthik; Myint, Myo Tay Zar; Dobretsov, Sergey; Richter, Jutta; Dutta, Joydeep

    2017-06-15

    Aquaculture is a billion dollar industry and biofouling of aquaculture installations has heavy economic penalties. The natural antifouling (AF) defence mechanism of some seaweed that inhibits biofouling by production of reactive oxygen species (ROS) inspired us to mimic this process by fabricating ZnO photocatalytic nanocoating. AF activity of fishing nets modified with ZnO nanocoating was compared with uncoated nets (control) and nets painted with copper-based AF paint. One month experiment in tropical waters showed that nanocoatings reduce abundances of microfouling organisms by 3-fold compared to the control and had higher antifouling performance over AF paint. Metagenomic analysis of prokaryotic and eukaryotic fouling organisms using next generation sequencing platform proved that nanocoatings compared to AF paint were not selectively enriching communities with the resistant and pathogenic species. The proposed bio-inspired nanocoating is an important contribution towards environmentally friendly AF technologies for aquaculture.

  5. Improved photocatalytic degradation of Orange G using hybrid nanofibers

    Energy Technology Data Exchange (ETDEWEB)

    Ledwaba, Mpho; Masilela, Nkosiphile; Nyokong, Tebello; Antunes, Edith, E-mail: ebeukes@uwc.ac.za [Rhodes University, Department of Chemistry (South Africa)

    2017-05-15

    Functionalised electrospun polyamide-6 (PA-6) nanofibres incorporating gadolinium oxide nanoparticles conjugated to zinc tetracarboxyphenoxy phthalocyanine (ZnTCPPc) as the sensitizer were prepared for the photocatalytic degradation of Orange G. Fibres incorporating the phthalocyanine alone or a mixture of the nanoparticles and phthalocyanine were also generated. The singlet oxygen-generating ability of the sensitizer was shown to be maintained within the fibre mat, with the singlet oxygen quantum yields increasing upon incorporation of the magnetic nanoparticles. Consequently, the rate of the photodegradation of Orange G was observed to increase with an increase in singlet oxygen quantum yield. A reduction in the half-lives for the functionalised nanofibres was recorded in the presence of the magnetic nanoparticles, indicating an improvement in the efficiency of the degradation process.

  6. Energy and Molecules from Photochemical/Photocatalytic Reactions. An Overview

    Directory of Open Access Journals (Sweden)

    Davide Ravelli

    2015-01-01

    Full Text Available Photocatalytic reactions have been defined as those processes that require both a (not consumed catalyst and light. A previous definition was whether such reactions brought a system towards or away from the (thermal equilibrium. This consideration brings in the question whether a part of the photon energy is incorporated into the photochemical reaction products. Data are provided for representative organic reactions involving or not molecular catalysts and show that energy storage occurs only when a heavily strained structure is generated, and in that case only a minor part of photon energy is actually stored (ΔG up to 25 kcal·mol−1. The green role of photochemistry/photocatalysis is rather that of forming highly reactive intermediates under mild conditions.

  7. Treatment of atrazine by integrating photocatalytic and biological processes

    International Nuclear Information System (INIS)

    Chan, C.Y.; Tao, S.; Dawson, R.; Wong, P.K.

    2004-01-01

    This research examines the degradation of atrazine by photocatalytic oxidation (PCO) under different experimental conditions. Deisopropylatrazine, deethylatrazine and deethyldeisopropylatrazine were formed as major intermediates based on gas chromatography-mass spectrometry. The reaction mixture was found to be toxic towards two bioassays, i.e. the Microtox[reg] and amphipods survival tests even when atrazine was completely degraded by PCO within 2 h under optimized conditions. The results indicate that adding H 2 O 2 could significantly enhance the degradation of atrazine by PCO. Ammeline, ammelide and cyanuric acid (CA) became the major intermediates/products as detected by high performance liquid chromatography from 6th to the 40th h of PCO treatment. After 72 h PCO treatment, only CA was detectable in the reaction mixture. Further degradation of CA was carried out by a newly isolated CA-degrading bacterium, Sphingomonas capsulata. The photochemical pretreatment integrated with microbial degradation lead to the complete degradation and detoxification of atrazine

  8. BiVO4 nanoparticles: Preparation, characterization and photocatalytic activity

    Directory of Open Access Journals (Sweden)

    Venkataraman Sivakumar

    2015-12-01

    Full Text Available Bismuth vanadate (BiVO4 nanoparticles were synthesized by a simple thermal decomposition method. The synthesized bismuth vanadate nanoparticles were characterized by X-ray diffraction analysis, it is found that the synthesized sample belongs to monoclinic BiVO4. Fourier transform infrared spectroscopy confirms the formation of Bi-O bond in the sample. Ultraviolet–Visible (DRS-UV–Visible spectroscopy and photoluminescence spectroscopy reveal the optical property of the BiVO4 nanoparticles. The morphology was identified by both scanning electron microscopy and high-resolution transmission electron microscopy. Further, the photocatalytic activity of BiVO4 nanoparticles was investigated by photodegradation of methylene blue as a model organic pollutant.

  9. Fabrication and Photocatalytic Properties of ZnSe Nanorod Films

    Directory of Open Access Journals (Sweden)

    Jiajia Yin

    2016-01-01

    Full Text Available ZnSe nanorod films grown on fused quartz glass substrates via a simple two-step synthesis protocol were demonstrated to be environmentally safe and effective recyclable photocatalysts. These films showed greatly enhanced photocatalytic activity compared to pulsed laser deposition ZnSe films in the degradation of methyl orange dye solutions. The well-crystalized ZnSe nanorods had a length of 15 µm and a diameter of 200 nm and were densely grown on the substrate. The morphology, crystal structure, crystal phase, and photophysical properties of the ZnSe nanorod films were investigated using field-emission scanning electron microscopy (FE-SEM, UV-Vis spectroscopy, X-ray diffraction (XRD, transmission electron microscopy (TEM, and high resolution transmission electron microscopy (HRTEM.

  10. Solar photocatalytic degradation and detoxification of EU priority substances

    Energy Technology Data Exchange (ETDEWEB)

    Hincapie, M. [Facultad de Ingeniera Ambiental, Universidad de Medellin, Carrera 87 No. 30-65, P.O. Box 1983, Medellin (Colombia); Maldonado, M.I.; Oller, I.; Gernjak, W.; Malato, S. [Plataforma Solar de Almeria-CIEMAT, Carretera Senes km4, 04200 Tabernas (Almeria) (Spain); Sanchez-Perez, J.A.; Ballesteros, M.M. [Departamento de Ingenieria Quimica, Universidad de Almeria Crta de Sacramento s/n, 04120 Almeria (Spain)

    2005-04-15

    Several different pesticides (alachlor, atrazine, chlorfenvinphos, diuron, isoproturon and pentachlorophenol) considered PS (priority substances) by the European Commission and dissolved in water at 50mg/L (or at maximum water solubility) have been degraded at pilot-plant scale using photo-Fenton and TiO{sub 2} photocatalysis driven by solar energy. Two different iron concentrations (2 and 55mg/L) and TiO{sub 2} at 200mg/L have been tested and discussed, using mainly TOC mineralisation for comparison of treatment effectiveness. Vibrio fischeri (Microtox{sup (}R)) toxicity assays were also employed for evaluating the photocatalytic treatments, and comparison between these results and parent compound disappearance, TOC evolution and anion (or ammonia) release were discussed. Almost complete mineralisation and total detoxification were always attained. It has been demonstrated that evolution of chloride could be a key-parameter for predicting toxicity of chlorinated compounds.

  11. Evaluation of photocatalytic treatment of industrial wastewater using solar energy

    International Nuclear Information System (INIS)

    Restrepo, Gloria Maria; Rios, Luis A; Marin, Juan Miguel; Montoya, Juan Felipe; Velasquez, Jorge Armando

    2008-01-01

    Wastewater of a chemical industry was treated in a photocatalytic process, using a solar photo-reactor made of glass corrugated flat plates that had been set in cascade and using Titanium Dioxide (Degussa p-25) as photocatalyst that is supported on each one of them in film form. the influence of three variables in the decontamination efficiency were studied: amount of H 2 O 2 , volume of water and amount of dispersed TiO 2 , by means of the accomplishment of fifteen experiments carried out in discontinuous operation mode by a period of 5 hours for each test. The obtained results allow establishing that the FH is a viable technology of treatment like previous stage to a biological treatment since percentage of reduction in the DQO varies between 6 and 46% and was managed to reach a biodegradable effluent in all tests

  12. Photocatalytic Iron Oxide Micro-Swimmers for Environmental Remediation

    Science.gov (United States)

    Richard, Cynthia; Simmchen, Juliane; Eychmüller, Alexander

    2018-05-01

    Harvesting energy from photochemical reactions has long been studied as an efficient means of renewable energy, a topic that is increasingly gaining importance also for motion at the microscale. Iron oxide has been a material of interest in recent studies. Thus, in this work different synthesis methods and encapsulation techniques were used to try and optimize the photo-catalytic properties of iron oxide colloids. Photodegradation experiments were carried out following the encapsulation of the nanoparticles and the Fenton effect was also verified. The end goal would be to use the photochemical degradation of peroxide to propel an array of swimmers in a controlled manner while utilizing the Fenton effect for the degradation of dyes or waste in wastewater remediation.

  13. Investigation of polypyrrole/polyvinyl alcohol–titanium dioxide composite films for photo-catalytic applications

    Energy Technology Data Exchange (ETDEWEB)

    Cao, Shaoqiang; Zhang, Hongyang; Song, Yuanqing; Zhang, Jianling; Yang, Haigang; Jiang, Long, E-mail: jianglong@scu.edu.cn; Dan, Yi, E-mail: danyichenweiwei@163.com

    2015-07-01

    Graphical abstract: - Highlights: • The study provides an easy and convenient method to fabricate films, which will give guidance for the preparation of three-dimensional materials. • The PPy/PVA–TiO{sub 2} films can keep better photo-catalytic activities both under UV and visible light irradiation when compared with TiO{sub 2} film. • There exist electron transfers between PPy/PVA and TiO{sub 2}. - Abstract: Polypyrrole/polyvinyl alcohol–titanium dioxide (PPy/PVA–TiO{sub 2}) composite films used as photo-catalysts were fabricated by combining TiO{sub 2} sol with PPy/PVA solution in which PPy was synthesized by in situ polymerization of pyrrole (Py) in polyvinyl alcohol (PVA) matrix and loaded on glass. The prepared photo-catalysts were investigated by X-ray diffraction (XRD), ultraviolet–visible diffuse reflection spectroscopy (UV–vis DRS), scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectra and photoluminescence (PL). The results indicate that the composites have same crystal structure as the TiO{sub 2} and extend the optic absorption from UV region to visible light region. By detecting the variation ratio, detected by ultraviolet–vis spectroscopy, of model pollutant rhodamine B (RhB) solution in the presence of the composite films under both UV and visible light irradiation, the photo-catalytic performance of the composite films was investigated. The results show that the PPy/PVA–TiO{sub 2} composite films show better photo-catalytic properties than TiO{sub 2} film both under UV and visible light irradiation, and the photo-catalytic degradation of RhB follows the first-order kinetics. The effects of the composition of composite films and the concentration of RhB on the photo-catalytic performance, as well as the possible photo-catalytic mechanism, were also discussed. By photo-catalytic recycle experiments, the structure stability of the PPy/PVA–TiO{sub 2} composite film was investigated and the results show that

  14. Recent Advances in Heterogeneous Photocatalytic Decolorization of Synthetic Dyes

    Science.gov (United States)

    Muhd Julkapli, Nurhidayatullaili; Bagheri, Samira; Bee Abd Hamid, Sharifah

    2014-01-01

    During the process and operation of the dyes, the wastes produced were commonly found to contain organic and inorganic impurities leading to risks in the ecosystem and biodiversity with the resultant impact on the environment. Improper effluent disposal in aqueous ecosystems leads to reduction of sunlight penetration which in turn diminishes photosynthetic activity, resulting in acute toxic effects on the aquatic flora/fauna and dissolved oxygen concentration. Recently, photodegradation of various synthetic dyes has been studied in terms of their absorbance and the reduction of oxygen content by changes in the concentration of the dye. The advantages that make photocatalytic techniques superior to traditional methods are the ability to remove contaminates in the range of ppb, no generation of polycyclic compounds, higher speed, and lower cost. Semiconductor metal oxides, typically TiO2, ZnO, SnO, NiO, Cu2O, Fe3O4, and also CdS have been utilized as photocatalyst for their nontoxic nature, high photosensitivity, wide band gap and high stability. Various process parameters like photocatalyst dose, pH and initial dye concentrations have been varied and highlighted. Research focused on surface modification of semiconductors and mixed oxide semiconductors by doping them with noble metals (Pt, Pd, Au, and Ag) and organic matter (C, N, Cl, and F) showed enhanced dye degradation compared to corresponding native semiconductors. This paper reviews recent advances in heterogeneous photocatalytic decolorization for the removal of synthetic dyes from water and wastewater. Thus, the main core highlighted in this paper is the critical selection of semiconductors for photocatalysis based on the chemical, physical, and selective nature of the poisoning dyes. PMID:25054183

  15. The suitability of silicon carbide for photocatalytic water oxidation

    Science.gov (United States)

    Aslam, M.; Qamar, M. T.; Ahmed, Ikram; Rehman, Ateeq Ur; Ali, Shahid; Ismail, I. M. I.; Hameed, Abdul

    2018-04-01

    Silicon carbide (SiC), owing to its extraordinary chemical stability and refractory properties, is widely used in the manufacturing industry. Despite the semiconducting nature and morphology-tuned band gap, its efficacy as photocatalysts has not been thoroughly investigated. The current study reports the synthesis, characterization and the evaluation of the capability of silicon carbide for hydrogen generation from water splitting. The optical characterization of the as-synthesized powder exposed the formation of multi-wavelength absorbing entities in synthetic process. The structural analysis by XRD and the fine microstructure analysis by HRTEM revealed the cubic 3C-SiC (β-SiC) and hexagonal α-polymorphs (2H-SiC and 6H-SiC) as major and minor phases, respectively. The Mott-Schottky analysis verified the n-type nature of the material with the flat band potential of - 0.7 V. In the electrochemical evaluation, the sharp increase in the peak currents in various potential ranges, under illumination, revealed the plausible potential of the material for the oxidation of water and generation of hydrogen. The generation of hydrogen and oxygen, as a consequence of water splitting in the actual photocatalytic experiments, was observed and measured. A significant increase in the yield of hydrogen was noticed in the presence of methanol as h + scavenger, whereas a retarding effect was offered by the Fe3+ entities that served as e - scavengers. The combined effect of both methanol and Fe3+ ions in the photocatalytic process was also investigated. Besides hydrogen gas, the other evolved gasses such as methane and carbon monoxide were also measured to estimate the mechanism of the process.

  16. Recent Advances in Heterogeneous Photocatalytic Decolorization of Synthetic Dyes

    Directory of Open Access Journals (Sweden)

    Nurhidayatullaili Muhd Julkapli

    2014-01-01

    Full Text Available During the process and operation of the dyes, the wastes produced were commonly found to contain organic and inorganic impurities leading to risks in the ecosystem and biodiversity with the resultant impact on the environment. Improper effluent disposal in aqueous ecosystems leads to reduction of sunlight penetration which in turn diminishes photosynthetic activity, resulting in acute toxic effects on the aquatic flora/fauna and dissolved oxygen concentration. Recently, photodegradation of various synthetic dyes has been studied in terms of their absorbance and the reduction of oxygen content by changes in the concentration of the dye. The advantages that make photocatalytic techniques superior to traditional methods are the ability to remove contaminates in the range of ppb, no generation of polycyclic compounds, higher speed, and lower cost. Semiconductor metal oxides, typically TiO2, ZnO, SnO, NiO, Cu2O, Fe3O4, and also CdS have been utilized as photocatalyst for their nontoxic nature, high photosensitivity, wide band gap and high stability. Various process parameters like photocatalyst dose, pH and initial dye concentrations have been varied and highlighted. Research focused on surface modification of semiconductors and mixed oxide semiconductors by doping them with noble metals (Pt, Pd, Au, and Ag and organic matter (C, N, Cl, and F showed enhanced dye degradation compared to corresponding native semiconductors. This paper reviews recent advances in heterogeneous photocatalytic decolorization for the removal of synthetic dyes from water and wastewater. Thus, the main core highlighted in this paper is the critical selection of semiconductors for photocatalysis based on the chemical, physical, and selective nature of the poisoning dyes.

  17. Fuels characterization studies. [jet fuels

    Science.gov (United States)

    Seng, G. T.; Antoine, A. C.; Flores, F. J.

    1980-01-01

    Current analytical techniques used in the characterization of broadened properties fuels are briefly described. Included are liquid chromatography, gas chromatography, and nuclear magnetic resonance spectroscopy. High performance liquid chromatographic ground-type methods development is being approached from several directions, including aromatic fraction standards development and the elimination of standards through removal or partial removal of the alkene and aromatic fractions or through the use of whole fuel refractive index values. More sensitive methods for alkene determinations using an ultraviolet-visible detector are also being pursued. Some of the more successful gas chromatographic physical property determinations for petroleum derived fuels are the distillation curve (simulated distillation), heat of combustion, hydrogen content, API gravity, viscosity, flash point, and (to a lesser extent) freezing point.

  18. Alternative Fuels Data Center: Ethanol Fueling Stations

    Science.gov (United States)

    ... More in this section... Ethanol Basics Benefits & Considerations Stations Locations Infrastructure fueling stations by location or along a route. Infrastructure Development Learn about ethanol fueling infrastructure; codes, standards, and safety; and ethanol equipment options. Maps & Data E85 Fueling Station

  19. Alternative Fuels Data Center: Biodiesel Fueling Stations

    Science.gov (United States)

    Locations Infrastructure Development Vehicles Laws & Incentives Biodiesel Fueling Stations Photo of a location or along a route. Infrastructure Development Learn about biodiesel fueling infrastructure codes Case Studies California Ramps Up Biofuels Infrastructure Green Fueling Station Powers Fleets in Upstate

  20. Fuels processing for transportation fuel cell systems

    Science.gov (United States)

    Kumar, R.; Ahmed, S.

    Fuel cells primarily use hydrogen as the fuel. This hydrogen must be produced from other fuels such as natural gas or methanol. The fuel processor requirements are affected by the fuel to be converted, the type of fuel cell to be supplied, and the fuel cell application. The conventional fuel processing technology has been reexamined to determine how it must be adapted for use in demanding applications such as transportation. The two major fuel conversion processes are steam reforming and partial oxidation reforming. The former is established practice for stationary applications; the latter offers certain advantages for mobile systems and is presently in various stages of development. This paper discusses these fuel processing technologies and the more recent developments for fuel cell systems used in transportation. The need for new materials in fuels processing, particularly in the area of reforming catalysis and hydrogen purification, is discussed.

  1. Fuel assembly

    International Nuclear Information System (INIS)

    Kurihara, Kunitoshi; Azekura, Kazuo.

    1992-01-01

    In a reactor core of a heavy water moderated light water cooled pressure tube type reactor, no sufficient effects have been obtained for the transfer width to a negative side of void reactivity change in a region of a great void coefficient. Then, a moderation region divided into upper and lower two regions is disposed at the central portion of a fuel assembly. Coolants flown into the lower region can be discharged to the cooling region from an opening disposed at the upper end portion of the lower region. Light water flows from the lower region of the moderator region to the cooling region of the reactor core upper portion, to lower the void coefficient. As a result, the reactivity performance at low void coefficient, i.e., a void reaction rate is transferred to the negative side. Thus, this flattens the power distribution in the fuel assembly, increases the thermal margin and enables rapid operaiton and control of the reactor core, as well as contributes to the increase of fuel burnup ratio and reduction of the fuel cycle cost. (N.H.)

  2. Fuel assembly

    International Nuclear Information System (INIS)

    Fushimi, Atsushi; Shimada, Hidemitsu; Aoyama, Motoo; Nakajima, Junjiro

    1998-01-01

    In a fuel assembly for an n x n lattice-like BWR type reactor, n is determined to 9 or greater, and the enrichment degree of plutonium is determined to 4.4% by weight or less. Alternatively, n is determined to 10 or greater, and the enrichment degree of plutonium is determined to 5.2% by weight or less. An average take-out burnup degree is determined to 39GWd/t or less, and the matrix is determined to 9 x 9 or more, or the average take-out burnup degree is determined to 51GWd/t, and the matrix is determined to 10 x 10 or more and the increase of the margin of the maximum power density obtained thereby is utilized for the compensation of the increase of distortion of power distribution due to decrease of the kinds of plutonium enrichment degree, thereby enabling to reduce the kind of the enrichment degree of MOX fuel rods to one. As a result, the manufacturing step for fuel pellets can be simplified to reduce the manufacturing cost for MOX fuel assemblies. (N.H.)

  3. Fuel rods

    International Nuclear Information System (INIS)

    Fukushima, Kimichika.

    1984-01-01

    Purpose: To reduce the size of the reactor core upper mechanisms and the reactor container, as well as decrease the nuclear power plant construction costs in reactors using liquid metals as the coolants. Constitution: Isotope capturing devices comprising a plurality of pipes are disposed to the gas plenum portion of a nuclear fuel rod main body at the most downstream end in the flowing direction of the coolants. Each of the capturing devices is made of nickel, nickel alloys, stainless steel applied with nickel plating on the surface, nickel alloys applied with nickel plating on the surface or the like. Thus, radioactive nuclides incorporated in the coolants are surely captured by the capturing devices disposed at the most downstream end of the nuclear fuel main body as the coolants flow along the nuclear fuel main body. Accordingly, since discharging of radioactive nuclides to the intermediate fuel exchange system can be prevented, the maintenance or reparing work for the system can be facilitated. (Moriyama, K.)

  4. Transport fuel

    DEFF Research Database (Denmark)

    Ronsse, Frederik; Jørgensen, Henning; Schüßler, Ingmar

    2014-01-01

    Worldwide, the use of transport fuel derived from biomass increased four-fold between 2003 and 2012. Mainly based on food resources, these conventional biofuels did not achieve the expected emission savings and contributed to higher prices for food commod - ities, especially maize and oilseeds...

  5. UV-A photocatalytic treatment of Legionella pneumophila bacteria contaminated airflows through three-dimensional solid foam structured photocatalytic reactors

    Energy Technology Data Exchange (ETDEWEB)

    Josset, Sebastien; Hajiesmaili, Shabnam; Begin, Dominique; Edouard, David; Pham-Huu, Cuong [Laboratoire des Materiaux, Surfaces et Procedes pour la Catalyse (LMSPC), European Laboratory for Catalysis and Surface Sciences (ELCASS), CNRS, Strasbourg University, 25 rue Becquerel 67087 Strasbourg (France); Lett, Marie-Claire [Laboratoire de Genetique Moleculaire, Genomique, Microbiologie, CNRS, Strasbourg University, 28, rue Goethe 67083 Strasbourg Cedex (France); Keller, Nicolas, E-mail: nkeller@chimie.u-strasbg.fr [Laboratoire des Materiaux, Surfaces et Procedes pour la Catalyse (LMSPC), European Laboratory for Catalysis and Surface Sciences (ELCASS), CNRS, Strasbourg University, 25 rue Becquerel 67087 Strasbourg (France); Keller, Valerie [Laboratoire des Materiaux, Surfaces et Procedes pour la Catalyse (LMSPC), European Laboratory for Catalysis and Surface Sciences (ELCASS), CNRS, Strasbourg University, 25 rue Becquerel 67087 Strasbourg (France)

    2010-03-15

    A 3D-structured photocatalytic media was designed for allowing a tubular reactor to work in a traversing-flow mode at low pressure drops with a strong increase in the surface area-to-volume ratio inside the reactor. A protective polysiloxane coating was performed for protecting a structured polyurethane foam and anchoring the active TiO{sub 2} particles. Filled with the 3D-structured solid foam supporting TiO{sub 2} photocatalyst, the reactor could thus take advantages from the static mixer effect and from the low pressure drop resulting from the reticulated foam support. Very efficient decontamination levels towards airborne Legionella pneumophila bacteria were reached in a single-pass test mode.

  6. Effect of Sr/Ti Ratio on the Photocatalytic Properties of SrTiO3

    International Nuclear Information System (INIS)

    Sulaeman, U; Yin, S; Sato, T

    2011-01-01

    Since strontium titanate is a wide gap semiconductor, it requires UV light to generate the photocatalytic activities. Modification of strontium titanate to show photocatalytic activity under visible light irradiation is the essential work to efficiently utilize the sun light energy for environmental application. It is expected that the synthesis of SrTiO 3 with variation of Sr/Ti atomic ratio could induce the defect crystals having unique photocatalytic properties. The SrTiO 3 with various Sr/Ti atomic ratios were synthesized by microwave-assisted solvothermal reaction of SrCl 2 .6H 2 O and Ti(OC 3 H 7 ) 4 in KOH aqueous solutions with different atomic ratios of Sr/Ti. The products were characterized by TG-DTA, XRD and DRS. The photocatalytic activity was determined by DeNO x ability using LED lamps with the wavelengths of 627 nm (red), 530 nm (green), 445 nm (blue) and 390 nm (UV). The nanoparticles of perovskite type SrTiO 3 with the particle size of 30-40 nm were successfully synthesized. The visible light responsive photocatalytic activity was generated by adding excess amount of Sr. The photocatalytic activity in visible light could be enhanced by an increase in the Sr/Ti atomic ratio up to 1.25, indicating that the visible light responsive photocatalytic activity is due to the generation of new band gap between the conduction band and valence band of SrTiO 3 by the formation of oxygen vacancy.

  7. Preparation of BiOBr thin films with micro-nano-structure and their photocatalytic applications

    Energy Technology Data Exchange (ETDEWEB)

    Li, Rui [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Fan, Caimei, E-mail: fancm@163.com [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Zhang, Xiaochao, E-mail: zhang13598124761@163.com [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Wang, Yawen; Wang, Yunfang [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Zhang, Hui [Particle Technology Research Centre, Department of Chemical and Biochemical Engineering, The University of Western Ontario, London, Ontario N6A 5B9 (Canada)

    2014-07-01

    A series of micro-nano-structure BiOBr thin films were prepared at a low temperature by the alcoholysis-coating method using BiBr{sub 3} as precursor. The as-prepared films were characterized by X-ray powder diffraction, scanning electron microscopy, and Brunauer–Emmett–Teller surface area. The obtained results indicated that micro-nano-structure tetragonal BiOBr films with different intensity ratios of (110) to (102) characteristic peaks could be synthesized through controlling the reaction temperature and the calcination temperatures. Furthermore, the photocatalytic activities of BiOBr thin films with different preparation conditions have been evaluated by the degradation of methyl orange (MO) under UV light irradiation, suggesting that the photocatalytic activity should be closely related to the solvent, the alcoholysis reaction temperature, and the calcining temperature. The best photocatalytic degradation efficiency of MO for BiOBr thin films reaches 98.5% under 2.5 h UV irradiation. The BiOBr thin films display excellent stability and their photocatalytic activity still remains above 90% after being used five times. The main reasons for the higher photocatalytic activity of micro-nano-structure BiOBr microspheres have been investigated. In addition, the possible formation mechanism of BiOBr thin films with micro-nano-structure and excellent photocatalytic activity was proposed and discussed. - Highlights: • The BiOBr film was prepared at low temperature via alcoholysis-coating method. • The optimum process conditions of preparing BiOBr film were discussed. • As-prepared BiOBr films were composed of micro-nano flake structures. • The BiOBr films demonstrated excellent photocatalytic activity. • The formation mechanism of BiOBr films with high activity was proposed.

  8. PHOTOCATALYTIC ACTIVITIES of Ag+ DOPED ZIF-8 and ZIF-L CRYSTALS

    Directory of Open Access Journals (Sweden)

    Berna Topuz

    2016-09-01

    Full Text Available Photocatalysis is expected to contribute to the solution of environmental problems such as water and air pollution in the near future. The design of photocatalysts with high electron-hole generation rates, high surface areas and high light absorption capacities is crucial in producing sustainable and cost-effective photocatalytic processes. Titania, zirconia, copper oxide, zinc oxide, iron oxide are widely used photocatalysts which have good light absorption capacities with moderate surface areas depending on the synthesis conditions. In the last decade metal organic frameworks (MOFs have been used in photocatalytic applications due to their very high surface areas up to 1000s of m2/g and adequate light absorption capacities. In this study zeolitic imidazolate framework (ZIF based MOF photocatalytsts were prepared and the effect of silver (Ag doping on the photocatalytic activity of ZIF-8 and ZIF-L crystals was investigated. Ag doped ZIF-8 and ZIF-L crystals were prepared and their activities in the photocatalytic removal of methylene blue (MB dye under UV irradiation were determined for the first time in the literature. Doped ZIF-8 and ZIF-L crystals showed better photocatalytic activities compared to the undoped crystals. 100% of MB was removed with 5 mole% Ag+ doped ZIF-8 in 40 min. The photocatalytic activity decreased beyond 5% doping level since Ag+ ions may have segregated due to a possible solid state solubility limit of Ag+ ions in the crystal lattice of ZIF-8. ZIF-L crystals possessed lower photocatalytic activities compared to ZIF-8 crystals.

  9. Photocatalytic degradation of an azo-dye on TiO2/activated carbon composite material.

    Science.gov (United States)

    Andriantsiferana, C; Mohamed, E F; Delmas, H

    2014-01-01

    A sequential adsorption/photocatalytic regeneration process to remove tartrazine, an azo-dye in aqueous solution, has been investigated. The aim ofthis work was to compare the effectiveness of an adsorbent/photocatalyst composite-TiO2 deposited onto activated carbon (AC) - and a simple mixture of powders of TiO2 and AC in same proportion. The composite was an innovative material as the photocatalyst, TiO2, was deposited on the porous surface ofa microporous-AC using metal-organic chemical vapour deposition in fluidized bed. The sequential process was composed of two-batch step cycles: every cycle alternated a step of adsorption and a step of photocatalytic oxidation under ultra-violet (365 nm), at 25 degreeC and atmospheric pressure. Both steps, adsorption and photocatalytic oxidation, have been investigated during four cycles. For both materials, the cumulated amounts adsorbed during four cycles corresponded to nearly twice the maximum adsorption capacities qmax proving the photocatalytic oxidation to regenerate the adsorbent. Concerning photocatalytic oxidation, the degree of mineralization was higher with the TiO2/AC composite: for each cycle, the value of the total organic carbon removal was 25% higher than that obtained with the mixture powder. These better photocatalytic performances involved better regeneration than higher adsorbed amounts for cycles 2, 3 and 4. Better performances with this promising material - TiO2 deposited onto AC - compared with TiO2 powder could be explained by the vicinity of photocatalytic and AC adsorption sites.

  10. Thorium fuel cycle management

    International Nuclear Information System (INIS)

    Zajac, R.; Darilek, P.; Breza, J.; Necas, V.

    2010-01-01

    In this presentation author deals with the thorium fuel cycle management. Description of the thorium fuels and thorium fuel cycle benefits and challenges as well as thorium fuel calculations performed by the computer code HELIOS are presented.

  11. Repairing fuel for reinsertion

    International Nuclear Information System (INIS)

    Krukshenk, A.

    1986-01-01

    Eqiupment for nuclear reactor fuel assembly repairing produced by Westinghouse and Brawn Bovery companies is described. Repair of failed fuel assemblies replacement of defect fuel elements gives a noticeable economical effect. Thus if the cost of a new fuel assembly is 450-500 thousand dollars, the replacement of one fuel element in it costs approximately 40-60 thousand dollars. In simple cases repairing includes either removal of failed fuel elements from a fuel assembly and its reinsertion with the rest of fuel elements into the reactor core (reactor refueling), or replacement of unfailed fuel elements from one fuel assembly to a new one (fuel assembly overhaul and reconditioning)

  12. Nuclear power fuel cycle

    International Nuclear Information System (INIS)

    Havelka, S.; Jakesova, L.

    1982-01-01

    Economic problems are discussed of the fuel cycle (cost of the individual parts of the fuel cycle and the share of the fuel cycle in the price of 1 kWh), the technological problems of the fuel cycle (uranium ore mining and processing, uranium isotope enrichment, the manufacture of fuel elements, the building of long-term storage sites for spent fuel, spent fuel reprocessing, liquid and gaseous waste processing), and the ecologic aspects of the fuel cycle. (H.S.)

  13. Magnetic and photocatalytic response of Ag-doped ZnFeO nano-composites for photocatalytic degradation of reactive dyes in aqueous solution

    International Nuclear Information System (INIS)

    Mahmood, Asif; Ramay, Shahid Mahmood; Al-Zaghayer, Yousef S.; Imran, Muhammad; Atiq, Shahid; Al-Johani, Meshal S.

    2014-01-01

    Highlights: • Self-consistent sol–gel based auto-combustion route was used. • Photocatalytic degradation of reactive dyes in aqueous solution was investigated. • Due to Ag doping, band gap reduced. • Activity of Ag-doped samples was higher than that of un-doped ones. - Abstract: To investigate the photocatalytic degradation of reactive dyes in aqueous solution, pure ZnO and Fe/Ag-doped magnetic photocatalysts having nominal compositions of Zn 0.95−x Fe 0.05 Ag x O (x = 0.0, 0.05 and 0.1) have been synthesized via self-consistent sol–gel based auto-combustion route. Thermally stable samples were subsequently confirmed to exhibit wurtzite type hexagonal structure, characteristic of ZnO. The nature of chemical bonding was elaborated by Fourier transform analysis. Electron microscopic techniques were employed to investigate the structural morphology and to evaluate the particle size. Ferromagnetic nature of the Fe/Ag doped samples was revealed by vibrating sample magnetometry, enabling the photocatalytic samples to be re-collected magnetically for repeated usage. The enhanced photocatalytic activity in the degradation of methylene blue under UV light irradiation with 5 and 10 wt.% Ag/ZnFeO has been observed validating the potential applications of these materials in the field of photo-degradation of organic pollutants

  14. High performance nano-titania photocatalytic paper composite. Part II: Preparation and characterization of natural zeolite-based nano-titania composite sheets and study of their photocatalytic activity

    International Nuclear Information System (INIS)

    Ko, Seonghyuk; Fleming, Paul D.; Joyce, Margaret; Ari-Gur, Pnina

    2009-01-01

    A novel paper composite with high photocatalytic performance was fabricated using natural zeolite (clinoptilolite)-based nanosized TiO 2 . Photocatalytic materials, from sol-gel derived TiO 2 colloids to its coupling with zeolite, have been designed, prepared and characterized. As-prepared anatase TiO 2 on zeolite particles were readily used in photocatalytic paper, which revealed zeolite-TiO 2 particles dispersed on a dense network of fibers with microvoids. Natural zeolite-based TiO 2 composite sheets described here decomposed gaseous toluene very effectively after UV irradiation and its removal efficiency was higher than that accomplished by photocatalytic paper made with Degussa P25 TiO 2 or Ahlstrom commercial photocatalytic non-woven paper.

  15. Nanosized TiO[subscript 2] for Photocatalytic Water Splitting Studied by Oxygen Sensor and Data Logger

    Science.gov (United States)

    Zhang, Ruinan; Liu, Song; Yuan, Hongyan; Xiao, Dan; Choi, Martin M. F.

    2012-01-01

    Photocatalytic water splitting by semiconductor photocatalysts has attracted considerable attention in the past few decades. In this experiment, nanosized titanium dioxide (nano-TiO[subscript 2]) particles are used to photocatalytically split water, which is then monitored by an oxygen sensor. Sacrificial reagents such as organics (EDTA) and metal…

  16. Direct Z-scheme TiO2/CdS hierarchical photocatalyst for enhanced photocatalytic H2-production activity

    Science.gov (United States)

    Meng, Aiyun; Zhu, Bicheng; Zhong, Bo; Zhang, Liuyang; Cheng, Bei

    2017-11-01

    Photocatalytic H2 evolution, which utilizes solar energy via water splitting, is a promising route to deal with concerns about energy and environment. Herein, a direct Z-scheme TiO2/CdS binary hierarchical photocatalyst was fabricated via a successive ionic layer adsorption and reaction (SILAR) technique, and photocatalytic H2 production was measured afterwards. The as-prepared TiO2/CdS hybrid photocatalyst exhibited noticeably promoted photocatalytic H2-production activity of 51.4 μmol h-1. The enhancement of photocatalytic activity was ascribed to the hierarchical structure, as well as the efficient charge separation and migration from TiO2 nanosheets to CdS nanoparticles (NPs) at their tight contact interfaces. Moreover, the direct Z-scheme photocatalytic reaction mechanism was demonstrated to elucidate the improved photocatalytic performance of TiO2/CdS composite photocatalyst. The photoluminescence (PL) analysis of hydroxyl radicals were conducted to provide clues for the direct Z-scheme mechanism. This work provides a facile route for the construction of redox mediator-free Z-scheme photocatalytic system for photocatalytic water splitting.

  17. Synthesis, characterization and photocatalytic activity of NaNbO{sub 3}/ZnO heterojunction photocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Xu Hui; Liu Chengtang [School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); School of the Environment, Jiangsu University, Zhenjiang 212013 (China); Li Huaming, E-mail: lihm@ujs.edu.cn [School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Xu Yuanguo; Xia Jiexiang; Yin Sheng; Liu Ling [School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Wu Xiangyang [School of the Environment, Jiangsu University, Zhenjiang 212013 (China)

    2011-09-15

    Highlights: > There was no report to investigate the photocatalytic activity of NaNbO3/ZnO heterojunction. > The relationship between the photocatalytic activity and the structural features of the prepared catalysts was investigated through a systematic characterization analysis. > The possible photocatalytic mechanism was proposed. - Abstract: A series of NaNbO{sub 3}/ZnO heteronanostructures were synthesized with the hydrothermal method. Various characterization methods such as X-ray powder diffraction (XRD), scanning electronic microscope (SEM) and energy dispersive X-ray spectrometer (EDS), transmission electron microscope (TEM), X-ray photoelectron spectra (XPS) and diffuse reflectance spectra (DRS) were employed to investigate the structure, morphology and photocatalytic properties. The photocatalytic activity of the catalysts was evaluated by the degradation of methylene blue dye and the highest photocatalytic efficiency was observed when the content of NaNbO{sub 3} was 10 wt.%. The photocatalytic mechanism of the heterojunction was also discussed. The effective transformation of the photoexcited electron and holes restricted the recombination of charges, which was regarded as the main reason of the high photocatalytic activity.

  18. Band gap-engineered ZnO and Ag/ZnO by ball-milling method and their photocatalytic and Fenton-like photocatalytic activities

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Young In [School of Chemistry and Biochemistry, Yeungnam University, Gyeongsan, Gyeongbuk 38541 (Korea, Republic of); Jung, Hye Jin [Department of Mechanical Engineering, Chungnam National University, Daejeon 34134 (Korea, Republic of); Shin, Weon Gyu, E-mail: wgshin@cnu.ac.kr [Department of Mechanical Engineering, Chungnam National University, Daejeon 34134 (Korea, Republic of); Sohn, Youngku, E-mail: youngkusohn@ynu.ac.kr [School of Chemistry and Biochemistry, Yeungnam University, Gyeongsan, Gyeongbuk 38541 (Korea, Republic of)

    2015-11-30

    Graphical abstract: - Highlights: • Ag/ZnO hybrid materials were prepared by a ball-milling method. • Adsorption and photocatalytic dye degradation were tested for pure RhB under visible light. • Adsorption and photocatalytic dye degradation were tested for mixed dye (MO + RhB + MB) under visible light. • Fenton-like photocatalytic activity (H{sub 2}O{sub 2} addition effects) was examined. - Abstract: The hybridization of ZnO with Ag has been performed extensively to increase the efficiency of ZnO in various applications, including catalysis. In this study, a wet (w) and dry (d) ball-milling method was used to hybridize Ag with ZnO nanoparticles, and their physicochemical properties were examined. Visible light absorption was enhanced and the band gap was engineered by ball-milling and Ag hybridization. Their photocatalytic activities were tested with rhodamine B (RhB) and a mixed dye (methyl orange + RhB + methylene blue) under visible light irradiation. For pure RhB, the photocatalytic activity was decreased by ball-milling and was observed in the order of ZnO(d) < Ag/ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). For the degradation of RhB and methylene blue (MB) in the mixed dye (or the simulated real contaminated water), the photocatalytic activity was observed in the order of Ag/ZnO(d) < ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). When the photodegradation tested with H{sub 2}O{sub 2} addition, however, the Fenton-like photocatalytic activity was reversed and the ZnO(ref) showed the poorest activity for the degradation of RhB and methylene blue (MB). In the mixed dye over all the catalysts, methyl orange (MO) was degraded most rapidly. The relative degradation rates of RhB and MB were found to be dependent on the catalyst and reaction conditions.

  19. Band gap-engineered ZnO and Ag/ZnO by ball-milling method and their photocatalytic and Fenton-like photocatalytic activities

    International Nuclear Information System (INIS)

    Choi, Young In; Jung, Hye Jin; Shin, Weon Gyu; Sohn, Youngku

    2015-01-01

    Graphical abstract: - Highlights: • Ag/ZnO hybrid materials were prepared by a ball-milling method. • Adsorption and photocatalytic dye degradation were tested for pure RhB under visible light. • Adsorption and photocatalytic dye degradation were tested for mixed dye (MO + RhB + MB) under visible light. • Fenton-like photocatalytic activity (H 2 O 2 addition effects) was examined. - Abstract: The hybridization of ZnO with Ag has been performed extensively to increase the efficiency of ZnO in various applications, including catalysis. In this study, a wet (w) and dry (d) ball-milling method was used to hybridize Ag with ZnO nanoparticles, and their physicochemical properties were examined. Visible light absorption was enhanced and the band gap was engineered by ball-milling and Ag hybridization. Their photocatalytic activities were tested with rhodamine B (RhB) and a mixed dye (methyl orange + RhB + methylene blue) under visible light irradiation. For pure RhB, the photocatalytic activity was decreased by ball-milling and was observed in the order of ZnO(d) < Ag/ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). For the degradation of RhB and methylene blue (MB) in the mixed dye (or the simulated real contaminated water), the photocatalytic activity was observed in the order of Ag/ZnO(d) < ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). When the photodegradation tested with H 2 O 2 addition, however, the Fenton-like photocatalytic activity was reversed and the ZnO(ref) showed the poorest activity for the degradation of RhB and methylene blue (MB). In the mixed dye over all the catalysts, methyl orange (MO) was degraded most rapidly. The relative degradation rates of RhB and MB were found to be dependent on the catalyst and reaction conditions.

  20. Fuel trading

    International Nuclear Information System (INIS)

    2015-01-01

    A first part of this report proposes an overview of trends and predictions. After a synthesis on the sector changes and trends, it indicates and comments the most recent predictions for the consumption of refined oil products and for the turnover of the fuel wholesale market, reports the main highlights concerning the sector's life, and gives a dashboard of the sector activity. The second part proposes the annual report on trends and competition. It presents the main operator profiles and fuel categories, the main determining factors of the activity, the evolution of the sector context between 2005 and 2015 (consumptions, prices, temperature evolution). It analyses the evolution of the sector activity and indicators (sales, turnovers, prices, imports). Financial performances of enterprises are presented. The economic structure of the sector is described (evolution of the economic fabric, structural characteristics, French foreign trade). Actors are then presented and ranked in terms of turnover, of added value, and of result

  1. Fuel assembly

    International Nuclear Information System (INIS)

    Ueda, Makoto.

    1991-01-01

    In a fuel assembly in which spectral shift type moderator guide members are arranged, the moderator guide member has a flow channel resistance member, that provides flow resistance against the moderators, in the upstream of a moderator flowing channel, by which the ratio of removing coolants is set greater at the upstream than downstream. With such a constitution, the void distribution increasing upward in the channel box except for the portion of the moderator guide member is moderated by the increase of the area of the void region that expands downward in the guide member. Accordingly, the axial power distribution is flattened throughout the operation cycle and excess distortion is eliminated to improve the fuel integrity. (T.M.)

  2. Fuel element

    International Nuclear Information System (INIS)

    Hirose, Yasuo.

    1982-01-01

    Purpose: To increase the plenum space in a fuel element used for a liquid metal cooled reactor. Constitution: A fuel pellet is secured at one end with an end plug and at the other with a coil spring in a tubular container. A mechanism for fixing the coil spring composed of a tubular unit is mounted by friction with the inner surface of the tubular container. Accordingly, the recoiling force of the coil spring can be retained by fixing mechanism with a small volume, and since a large amount of plenum space can be obtained, the internal pressure rise in the cladding tube can be suppressed even if large quantities of fission products are discharged. (Kamimura, M.)

  3. Fuel assembly

    International Nuclear Information System (INIS)

    Kawai, Mitsuo.

    1988-01-01

    Purpose: To reduce the corrosion rate and suppress the increase of radioactive corrosion products in reactor water of nuclear fuel assemblies for use in BWR type reactors having spacer springs made of nickel based deposition reinforced type alloys. Constitution: Spacer rings made of nickel based deposition reinforced type alloy are incorporated and used as fuel assemblies after applying treatment of dipping and maintaining at high temperature water followed by heating in steams. Since this can remove the nickel leaching into reactor water at the initial stage, Co-58 as the radioactive corrosion products in the reactor water can be reduced, and the operation at in-service inspection or repairement can be facilitated to improve the working efficiency of the nuclear power plant. The dipping time is desirably more than 10 hours and more desirably more than 30 hours. (Horiuchi, T. )

  4. Fuel assemblies

    International Nuclear Information System (INIS)

    Yoshioka, Ritsuo.

    1983-01-01

    Purpose: To improve the operation performance of a BWR type reactor by improving the distribution of the uranium enrichment and the incorporation amount of burnable poisons in fuel assemblies. Constitution: The average enrichment of uranium 235 is increased in the upper portion as compared with that in the lower portion, while the incorporation amount of burnable poisons is increased in an upper portion as compared with that in the lower portion. The difference in the incorporation amount of the burnable poisons between the upper and lower portions is attained by charging two kinds of fuel rods; the ones incorporated with the burnable poisons over the entire length and the others incorporated with the burnable poisons only in the upper portions. (Seki, T.)

  5. Characterization of nanoparticles released during construction of photocatalytic pavements using engineered nanoparticles

    International Nuclear Information System (INIS)

    Dylla, Heather; Hassan, Marwa M.

    2012-01-01

    With the increasing use of titanium dioxide (TiO 2 ) nanoparticles in self-cleaning materials such as photocatalytic concrete pavements, the release of nanoparticles into the environment is inevitable. Nanoparticle concentration, particle size, surface area, elemental composition, and surface morphology are pertinent to determine the associated risks. In this study, the potential of exposure to synthetic nanoparticles released during construction activities for application of photocatalytic pavements was measured during laboratory-simulated construction activities of photocatalytic mortar overlays and in an actual field application of photocatalytic spray coat. A scanning mobility particle sizer system measured the size distribution of nanoparticles released during laboratory and field activities. Since incidental nanoparticles are released during construction activities, nanoparticle emissions were compared to those from similar activities without nano-TiO 2 . Nanoparticle counts and size distribution suggest that synthetic nanoparticles are released during application of photocatalytic pavements. In order to identify the nanoparticle source, nanoparticles were also collected for offline characterization using transmission electron microscopy. However, positive identification of synthetic nanoparticles was not possible due to difficulties in obtaining high-resolution images. As a result, further research is recommended to identify nanoparticle composition and sources.

  6. SiO2@TiO2 Coating: Synthesis, Physical Characterization and Photocatalytic Evaluation

    Directory of Open Access Journals (Sweden)

    A. Rosales

    2018-03-01

    Full Text Available Use of silicon dioxide (SiO2 and titanium dioxide (TiO2 have been widely investigated individually in coatings technology, but their combined properties promote compatibility for different innovative applications. For example, the photocatalytic properties of TiO2 coatings, when exposed to UV light, have interesting environmental applications, such as air purification, self-cleaning and antibacterial properties. However, as reported in different pilot projects, serious durability problems, associated with the adhesion between the substrate and TiO2, have been evidenced. Thus, the aim of this work is to synthesize SiO2 together with TiO2 to increase the durability of the photocatalytic coating without affecting its photocatalytic potential. Therefore, synthesis using sonochemistry, synthesis without sonochemistry, physical characterization, photocatalytic evaluation, and durability of the SiO2, SiO2@TiO2 and TiO2 coatings are presented. Results indicate that using SiO2 improved the durability of the TiO2 coating without affecting its photocatalytic properties. Thus, this novel SiO2@TiO2 coating shows potential for developing long-lasting, self-cleaning and air-purifying construction materials.

  7. The improvement of photocatalytic processes: Design of a photoreactor using high-power LEDs

    Directory of Open Access Journals (Sweden)

    Marzieh Khademalrasool

    2016-09-01

    Full Text Available This paper is an attempt to survey the benefits of a well-designed photoreactor containing just 6 ultraviolet (UV high power light emitting diodes (HPLEDs; the power and wavelength of each UV HPLED are 1 W and 365 nm, respectively, the latter being an efficient source for photocatalytic studies. Although the experiment with the 365-nm LEDs is reported here, other LEDs were predicted for conducting similar experiments including green photocatalytic ones. We installed diodes with respect to the luminescence intensity distribution curves (LIDCs or intensity patterns. Then, in order to compare the efficiency of the UV-HPLEDs of the HP-LED photoreactor (HPLED-PhR with that of traditional UV lamps which are extensively used in photocatalytic processes, a set of UV HPLEDs was designed and made up. Next, the performance of HPLED-PhR was compared with that of a traditional fluorescent lamp photoreactor (FL-PhR. As a typical photocatalytic experiment, Zinc Oxide (ZnO nanoparticles were synthesized via co-precipitation method and used as photocatalyst for purification of water polluted with the reactive blue dye (RB, under UV irradiation in two photoreactors. The results showed that the rate of photocatalytic reaction under the UV-LEDs was two times greater than the rate under the traditional fluorescent UV lamps, while both electrical power consumption and manufacturing cost of the HPLED-PhR were less than a quarter of them for the FL-PhR.

  8. Thiourea-Modified TiO2 Nanorods with Enhanced Photocatalytic Activity

    Directory of Open Access Journals (Sweden)

    Xiaofeng Wu

    2016-02-01

    Full Text Available Semiconductor TiO2 photocatalysis has attracted much attention due to its potential application in solving the problems of environmental pollution. In this paper, thiourea (CH4N2S modified anatase TiO2 nanorods were fabricated by calcination of the mixture of TiO2 nanorods and thiourea at 600 °C for 2 h. It was found that only N element was doped into the lattice of TiO2 nanorods. With increasing the weight ratio of thiourea to TiO2 (R from 0 to 8, the light-harvesting ability of the photocatalyst steady increases. Both the crystallization and photocatalytic activity of TiO2 nanorods increase first and then decrease with increase in R value, and R2 sample showed the highest crystallization and photocatalytic activity in degradation of Brilliant Red X3B (X3B and Rhodamine B (RhB dyes under visible light irradiation (λ > 420 nm. The increased visible-light photocatalytic activity of the prepared N-doped TiO2 nanorods is due to the synergistic effects of the enhanced crystallization, improved light-harvesting ability and reduced recombination rate of photo-generated electron-hole pairs. Note that the enhanced visible photocatalytic activity of N-doped nanorods is not based on the scarification of their UV photocatalytic activity.

  9. Preparation high photocatalytic activity of CdS/halloysite nanotubes (HNTs) nanocomposites with hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Xing Weinan [School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Ni Liang, E-mail: xingweinan3@126.com [School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China); Huo Pengwei; Lu Ziyang; Liu Xinlin; Luo Yingying; Yan Yongsheng [School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013 (China)

    2012-10-15

    Highlights: Black-Right-Pointing-Pointer CdS/halloysite nanotubes (HNTs) were synthesized by hydrothermal method. Black-Right-Pointing-Pointer The CdS/HNTs had better photocatalytic activity for degradation of tetracycline. Black-Right-Pointing-Pointer The presence of halloysite nanotubes both improved its photocatalytic activity and stability. - Abstract: A novel nanocatalyst CdS/halloysite nanotubes (HNTs) was synthesized by hydrothermal method with direct growth of CdS nanoparticles on the surface of HNTs. The as-prepared photocatalysts had been characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), UV-vis diffuse reflectance spectra (UV-vis DRS), Fourier transform infrared (FT-IR) and the thermo gravimetric analysis (TGA). The photocatalytic activity of the sample was evaluated by the degradation of tetracycline (TC) under visible light irradiation. Benefit from the excellent properties of CdS and HNTs, the photocatalyst exhibited good photocatalytic activity and stability. In order to find out the optimum synthesis condition to obtain the best photocatalytic activity, a series of experiments were performed with different CdS loading capacity, different sources of sulfide and different hydrothermal temperatures, etc. The best photodegradation rate could reach 93% in 60 min under visible light irradiation. Therefore, the combination of CdS nanoparticles with HNTs endowed this material with a potential use in environmental treatments in industries.

  10. Photocatalytic degradation of diuron in aqueous solution by platinized TiO2

    International Nuclear Information System (INIS)

    Katsumata, Hideyuki; Sada, Maki; Nakaoka, Yusuke; Kaneco, Satoshi; Suzuki, Tohru; Ohta, Kiyohisa

    2009-01-01

    The photocatalytic degradation of diuron, which is one of phenylurea herbicides, was carried out in the presence of platinized TiO 2 photocatalyst. Platinization was found to increase the rate of diuron degradation. When 0.2 wt.% of platinum was deposited onto the surface of TiO 2 , an initial diuron concentration of 10 mg L -1 was completely degraded after 20 min. Furthermore, the first-order rate constant for diuron degradation by Pt-TiO 2 was ca. 4 times higher than P-25 TiO 2 . In addition, the photocatalytic activity of Pt-TiO 2 was appeared under visible light. The decrease of TOC as a result of mineralization of diuron was observed during the photocatalytic process. The degree of diuron mineralization was about 97% under UV irradiation after 8 h. The formations of chloride, nitrate and ammonium ions as end-products were observed during the photocatalytic system. The decomposition of diuron gave four kinds of intermediate products. The degradation mechanism of diuron was proposed on the base of the evidence of the identified intermediates. Based on these results, the photocatalytic reaction by Pt-TiO 2 could be useful technology for the treatment of wastewater containing diuron.

  11. Biomolecule-assisted construction of cadmium sulfide hollow spheres with structure-dependent photocatalytic activity.

    Science.gov (United States)

    Wei, Chengzhen; Zang, Wenzhe; Yin, Jingzhou; Lu, Qingyi; Chen, Qun; Liu, Rongmei; Gao, Feng

    2013-02-25

    In this study, we report the synthesis of monodispersive solid and hollow CdS spheres with structure-dependent photocatalytic abilities for dye photodegradation. The monodispersive CdS nanospheres were constructed with the assistance of the soulcarboxymthyi chitosan biopolymer under hydrothermal conditions. The solid CdS spheres were corroded by ammonia to form hollow CdS nanospheres through a dissolution-reprecipitation mechanism. Their visible-light photocatalytic activities were investigated, and the results show that both the solid and the hollow CdS spheres have visible-light photocatalytic abilities for the photodegradation of dyes. The photocatalytic properties of the CdS spheres were demonstrated to be structure dependent. Although the nanoparticles comprising the hollow spheres have larger sizes than those comprising the solid spheres, the hollow CdS spheres have better photocatalytic performances than the solid CdS spheres, which can be attributed to the special hollow structure. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Preparation high photocatalytic activity of CdS/halloysite nanotubes (HNTs) nanocomposites with hydrothermal method

    International Nuclear Information System (INIS)

    Xing Weinan; Ni Liang; Huo Pengwei; Lu Ziyang; Liu Xinlin; Luo Yingying; Yan Yongsheng

    2012-01-01

    Highlights: ► CdS/halloysite nanotubes (HNTs) were synthesized by hydrothermal method. ► The CdS/HNTs had better photocatalytic activity for degradation of tetracycline. ► The presence of halloysite nanotubes both improved its photocatalytic activity and stability. - Abstract: A novel nanocatalyst CdS/halloysite nanotubes (HNTs) was synthesized by hydrothermal method with direct growth of CdS nanoparticles on the surface of HNTs. The as-prepared photocatalysts had been characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), UV–vis diffuse reflectance spectra (UV–vis DRS), Fourier transform infrared (FT-IR) and the thermo gravimetric analysis (TGA). The photocatalytic activity of the sample was evaluated by the degradation of tetracycline (TC) under visible light irradiation. Benefit from the excellent properties of CdS and HNTs, the photocatalyst exhibited good photocatalytic activity and stability. In order to find out the optimum synthesis condition to obtain the best photocatalytic activity, a series of experiments were performed with different CdS loading capacity, different sources of sulfide and different hydrothermal temperatures, etc. The best photodegradation rate could reach 93% in 60 min under visible light irradiation. Therefore, the combination of CdS nanoparticles with HNTs endowed this material with a potential use in environmental treatments in industries.

  13. Titanium dioxide encapsulation of supported Ag nanoparticles on the porous silica bead for increased photocatalytic activity

    International Nuclear Information System (INIS)

    Liu, Hui; Deng, Lu; Sun, Chaochao; Li, Junqi; Zhu, Zhenfeng

    2015-01-01

    Graphical abstract: - Highlights: • A novel Ag-loading and TiO 2 -coating technique was used to prepare samples. • The photocatalytic activity of the product was evaluated by removing of Rh B. • The as-synthesized samples showed an excellent photocatalytic activity. - Abstract: A new synthetic strategy has been developed to encapsulate Ag nanoparticles in heterogeneous catalysts to prevent their dropping and sintering. Ag nanoparticles with diameters about 5–10 nm were first supported on the porous silica bead. These were then covered with a fresh layer of titanium dioxide with the thickness about 5 nm. SEM and TEM images were used to confirm the success of each synthesis step, and the photocatalytic activity of the as-synthesized samples was evaluated by photocatalytic decolorization of Rhodamine B (Rh B) aqueous solution at ambient temperature under both UV and visible light irradiation. The resulting titanium dioxide encapsulated Ag nanoparticles exhibited an enhanced photocatalytic activity under both UV and visible light irradiation, this can be attributed to effective charge separation and light harvesting of the plasmonic silver nanoparticles decoration, even the reducing of the exciton recombination rate caused by the small grain size of anatase TiO 2 nanocrystals

  14. Hierarchical Layered WS2 /Graphene-Modified CdS Nanorods for Efficient Photocatalytic Hydrogen Evolution.

    Science.gov (United States)

    Xiang, Quanjun; Cheng, Feiyue; Lang, Di

    2016-05-10

    Graphene-based ternary composite photocatalysts with genuine heterostructure constituents have attracted extensive attention in photocatalytic hydrogen evolution. Here we report a new graphene-based ternary composite consisting of CdS nanorods grown on hierarchical layered WS2 /graphene hybrid (WG) as a high-performance photocatalyst for hydrogen evolution under visible light irradiation. The optimal content of layered WG as a co-catalyst in the ternary CdS/WS2 /graphene composites was found to be 4.2 wt %, giving a visible light photocatalytic H2 -production rate of 1842 μmol h(-1)  g(-1) with an apparent quantum efficiency of 21.2 % at 420 nm. This high photocatalytic H2 -production activity is due to the deposition of CdS nanorods on layered WS2 /graphene sheets, which can efficiently suppress charge recombination, improve interfacial charge transfer, and provide reduction active sites. The proposed mechanism for the enhanced photocatalytic activity of CdS nanorods modified with hierarchical layered WG was further confirmed by transient photocurrent response. This work shows that a noble-metal-free hierarchical layered WS2 /graphene nanosheets hybrid can be used as an effective co-catalyst for photocatalytic water splitting. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Photophysics and electrochemistry relevant to photocatalytic water splitting involved at solid–electrolyte interfaces

    KAUST Repository

    Shinagawa, Tatsuya

    2016-08-04

    Direct photon to chemical energy conversion using semiconductor-electrocatalyst-electrolyte interfaces has been extensively investigated for more than a half century. Many studies have focused on screening materials for efficient photocatalysis. Photocatalytic efficiency has been improved during this period but is not sufficient for industrial commercialization. Detailed elucidation on the photocatalytic water splitting process leads to consecutive six reaction steps with the fundamental parameters involved: The photocatalysis is initiated involving photophysics derived from various semiconductor properties (1: photon absorption, 2: exciton separation). The generated charge carriers need to be transferred to surfaces effectively utilizing the interfaces (3: carrier diffusion, 4: carrier transport). Consequently, electrocatalysis finishes the process by producing products on the surface (5: catalytic efficiency, 6: mass transfer of reactants and products). Successful photocatalytic water splitting requires the enhancement of efficiency at each stage. Most critically, a fundamental understanding of the interfacial phenomena is highly desired for establishing "photocatalysis by design" concepts, where the kinetic bottleneck within a process is identified by further improving the specific properties of photocatalytic materials as opposed to blind material screening. Theoretical modeling using the identified quantitative parameters can effectively predict the theoretically attainable photon-conversion yields. This article provides an overview of the state-of-the-art theoretical understanding of interfacial problems mainly developed in our laboratory. Photocatalytic water splitting (especially hydrogen evolution on metal surfaces) was selected as a topic, and the photophysical and electrochemical processes that occur at semiconductor-metal, semiconductor-electrolyte and metal-electrolyte interfaces are discussed.

  16. Photocatalytic Decolorization Study of Methyl Orange by TiO2–Chitosan Nanocomposites

    Directory of Open Access Journals (Sweden)

    Imelda Fajriati

    2014-10-01

    Full Text Available The photocatalytic decolorization of methyl orange (MO by TiO2-chitosan nanocomposite has been studied. This study was started by synthesizing TiO2-chitosan nanocomposites using sol-gel method with various concentrations of Titanium(IV isopropoxide (TTIP as the TiO2 precursor. The structure, surface morphology, thermal and optical property of TiO2-chitosan nanocomposite were characterized by X-ray diffraction (XRD, fourier transform infra red (FTIR spectroscopy, scanning electron microscopy (SEM, thermogravimetric analysis (TGA, and diffuse reflectance ultra violet (DRUV spectroscopy. The photocatalytic activity of TiO2-chitosan nanocomposite was evaluated by photocatalytic decolorization of methyl orange as a model pollutant. The results indicate that the particle size of TiO2 increases with increasing ofthe concentration of TTIP, in which TiO2 with smallest particle size exhibit the highest photocatalytic activity. The highest photocatalytic decolorization was obtained at 5 h of contact time, initial concentration of MO at 20 ppm and at solution pH of 4. Using these conditions, over 90% of MO was able to be decolorized using 0.02 g of TiO2-chitosan nanocomposite under UV light irradiation. The TiO2-chitosan nanocomposite could be reused, which meant that the TiO2-chitosan nanocomposites can be developed as an effective and economical photocatalyst to decolorize or treat dye in wastewater.

  17. Synthesis of graphene oxide-copper molybdate (GO-CuM) nanocomposites for photocatalytic application

    Science.gov (United States)

    Singh, Gajendar; Bhargava, V. Sai; Sharma, Manu

    2018-05-01

    Transition metal molybdates (TMBs) MMoO4 (M=Ni, Cu, Fe, Zn, Co, etc.) based nanocomposites have been considered as remarkable materials in the field of electronics, optics, catalysis, supercapicitors and energy storage devices. Nanocomposites of TMBs with graphene oxide have also been chosen as an effective material in photocatalytic application. GO-CuM nanocomposites were synthesized by ultra-sonication method at RT, followed by reflux route for preparation of CuM and GO by modified Hemmer's method. As prepared nanocomposites were characterized using analytical techniques such as PXRD, SEM, FT-IR and UV-Visible spectroscopy. The enhanced photocatalytic activity of Methylene blue (MB) dye was observed by GO-CuM nanocomposites as compared to pure copper molybdate. GO-CuM nanocomposites show high photodegradation rate (0.094 min-1) whereas CuM was degraded only 30 % with the rate of 0.0029 min-1. The high photocatalytic efficiency is due to the presence of graphene oxide that helps to delay the charge recombination in photocatalytic reaction The effect of the different amount of graphene oxide on the photocatalytic activity of as prepared photocatalyst has also been investigated.

  18. Photocatalytic degradation of diuron in aqueous solution by platinized TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Katsumata, Hideyuki, E-mail: hidek@chem.mie-u.ac.jp [Department of Chemistry for Materials, Graduate School of Engineering, Mie University, Tsu, Mie 514-8507 (Japan); Sada, Maki; Nakaoka, Yusuke; Kaneco, Satoshi [Department of Chemistry for Materials, Graduate School of Engineering, Mie University, Tsu, Mie 514-8507 (Japan); Suzuki, Tohru [Environmental Preservation Center, Mie University, Tsu, Mie 514-8507 (Japan); Ohta, Kiyohisa [Department of Chemistry for Materials, Graduate School of Engineering, Mie University, Tsu, Mie 514-8507 (Japan)

    2009-11-15

    The photocatalytic degradation of diuron, which is one of phenylurea herbicides, was carried out in the presence of platinized TiO{sub 2} photocatalyst. Platinization was found to increase the rate of diuron degradation. When 0.2 wt.% of platinum was deposited onto the surface of TiO{sub 2}, an initial diuron concentration of 10 mg L{sup -1} was completely degraded after 20 min. Furthermore, the first-order rate constant for diuron degradation by Pt-TiO{sub 2} was ca. 4 times higher than P-25 TiO{sub 2}. In addition, the photocatalytic activity of Pt-TiO{sub 2} was appeared under visible light. The decrease of TOC as a result of mineralization of diuron was observed during the photocatalytic process. The degree of diuron mineralization was about 97% under UV irradiation after 8 h. The formations of chloride, nitrate and ammonium ions as end-products were observed during the photocatalytic system. The decomposition of diuron gave four kinds of intermediate products. The degradation mechanism of diuron was proposed on the base of the evidence of the identified intermediates. Based on these results, the photocatalytic reaction by Pt-TiO{sub 2} could be useful technology for the treatment of wastewater containing diuron.

  19. Enhancing Photocatalytic Performance through Tuning the Interfacial Process between -Assembled and Pt-Loaded Microspheres

    Directory of Open Access Journals (Sweden)

    Jun Zhang

    2012-01-01

    Full Text Available This work reports on a simple two-step approach to rutile TiO2-assembled microspheres loaded by Pt with an aim to tune semiconductor-metal interfacial processes for enhancing the photocatalytic performance. Systematic sample characterizations and structural analysis indicate that Pt loading did not produce any significant influences on the lattice structure of TiO2-assembled microspheres. Instead, upon Pt loading, Schottky barrier was formed in the interfaces between microspheres and Pt nanoparticles, which inhabited efficiently the recombination of photo-generated electron-hole pairs essential for the photocatalytic activities. In addition, TiO2 microspheres also showed a capacity of electrons storage and releasing as represented by a high dielectric constant, which increased the utility rate of photogenerated electrons. All these structural advantages contribute to the excellent photocatalytic activity under ultraviolet light irradiation. The interfacial process between microspheres and Pt nanoparticles was further tuned through adjusting the loading Pt content of metal Pt. As a consequence, the best photocatalytic activity on TiO2 was obtained at 0.85 wt% Pt loading, above or below which photocatalytic activity was apparently decreased.

  20. Photocatalytic degradation of NOx gases using TiO2-containing paint: a real scale study.

    Science.gov (United States)

    Maggos, Th; Bartzis, J G; Liakou, M; Gobin, C

    2007-07-31

    An indoor car park was appropriately equipped in order to test the de-polluting efficiency of a TiO(2)-containing paint in an indoor polluted environment, under real scale configuration. Depollution tests were performed in an artificially closed area of the parking, which was polluted by a car exhaust during the testing period. The ceiling surface of the car park was covered with white acrylic TiO(2)-containing paint (PP), which was developed in the frame of the EU project 'PICADA' (Photocatalytic Innovative Coverings Application for Depollution Assessment). The closed area was fed with car exhaust gases. As soon as the system reached steady state, the UV lamps were turned on for 5h. The difference between the final and the initial steady state concentration indicates the removal of the pollutants due to both the photocatalytic paint and car emission reduction. Results showed a significant photocatalytic oxidation of NO(x) gases. The photocatalytic removal of NO and NO(2) was calculated to 19% and 20%, respectively, while the photocatalytic rate (microgm(-2)s(-1)) ranged between 0.05 and 0.13 for NO and between 0.09 and 0.16 for NO(2).

  1. Carbon dots/BiOCl films with enhanced visible light photocatalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Weitian; Yu, Xiang; Shen, Yinghua; Chen, Hongbin; Zhu, Yi, E-mail: tzhury@jnu.edu.cn; Zhang, Yuanming [Jinan University, Department of Chemistry (China); Meng, Hui [Jinan University, Siyuan laboratory, Guangzhou Key Laboratory of Vacuum Coating Technologies and New Energy Materials, Department of Physics (China)

    2017-02-15

    Novel carbon dots with a diameter of 6 nm modified BiOCl (CDs/BiOCl) photocatalyst on FTO was synthesized via a facile immobilization method at room temperature. The crystalline structures, morphologies, optical properties, and photocatalytic properties were studied. The results showed that the CDs/BiOCl films exhibited higher photocatalytic activity than pure BiOCl. The 4 wt% CDs/BiOCl film showed the best photocatalytic activity, which was about eight times than that of pure BiOCl and excellent recyclability even after four recycles. Compared with other film photocatalysts, the photocatalytic activity of 4 wt% CDs/BiOCl was also higher than that of many other photocatalysts. The enhanced activity was ascribed to the enhanced light adsorption and the improvement of charge separation. Holes and superoxide radicals ·O{sub 2}{sup −} were revealed as the dominant reactive species. The photocatalytic mechanism was proposed based on the results.

  2. Highly Efficient Photocatalytic Water Splitting over Edge-Modified Phosphorene Nanoribbons.

    Science.gov (United States)

    Hu, Wei; Lin, Lin; Zhang, Ruiqi; Yang, Chao; Yang, Jinlong

    2017-11-01

    Two-dimensional phosphorene with desirable optoelectronic properties (ideal band gap, high carrier mobility, and strong visible light absorption) is a promising metal-free photocatalyst for water splitting. However, the band edge positions of the valence band maximum (VBM) and conduction band maximum (CBM) of phosphorene are higher than the redox potentials in photocatalytic water splitting reactions. Thus, phosphorene can only be used as the photocathode for hydrogen evolution reaction as a low-efficiency visible-light-driven photocatalyst for hydrogen production in solar water splitting cells. Here, we propose a new mechanism to improve the photocatalytic efficiency of phosphorene nanoribbons (PNRs) by modifying their edges for full reactions in photocatalytic water splitting. By employing first-principles density functional theory calculations, we find that pseudohalogen (CN and OCN) passivated PNRs not only show desired VBM and CBM band edge positions induced by edge electric dipole layer, but also possess intrinsic optoelectronic properties of phosphorene, for both water oxidation and hydrogen reduction in photocatalytic water splitting without using extra energy. Furthermore, our calculations also predict that the maximum energy conversion efficiency of heterojunction solar cells consisting of different edge-modified PNRs can be as high as 20% for photocatalytic water splitting.

  3. Hierarchical synthesis of corrugated photocatalytic TiO{sub 2} microsphere architectures on natural pollen surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Erdogan, Deniz Altunoz; Ozensoy, Emrah, E-mail: ozensoy@fen.bilkent.edu.tr

    2017-05-01

    Highlights: • Biotemplate-based photocatalytic material was synthesized in the form of corrugated TiO{sub 2} microspheres. • Characterization of photocatalysts as a function of temperature. • Photocatalytic activities studied in the gas and solution phases. - Abstract: Biomaterials are challenging, yet vastly promising templates for engineering unusual inorganic materials with unprecedented surface and structural properties. In the current work, a novel biotemplate-based photocatalytic material was synthesized in the form of corrugated TiO{sub 2} microspheres by utilizing a sol-gel methodology where Ambrosia trifida (Ab, Giant ragweed) pollen was exploited as the initial biological support surface. Hierarchically synthesized TiO{sub 2} microspheres were structurally characterized in detail via SEM-EDX, Raman spectroscopy, XRD and BET techniques in order to shed light on the surface chemistry, crystal structure, chemical composition and morphology of these novel material architectures. Photocatalytic functionality of the synthesized materials was demonstrated both in gas phase as well as in liquid phase. Along these lines, air and water purification capabilities of the synthesized TiO{sub 2} microspheres were established by performing photocatalytic oxidative NOx(g) storage and Rhodamine B(aq) degradation experiments; respectively. The synthetic approach presented herein offers new opportunities to design and create sophisticated functional materials that can be used in micro reactor systems, adsorbents, drug delivery systems, catalytic processes, and sensor technologies.

  4. Bi2WO6 nanoflowers: An efficient visible light photocatalytic activity for ceftriaxone sodium degradation

    Science.gov (United States)

    Zhao, Yanyan; Wang, Yongbo; Liu, Enzhou; Fan, Jun; Hu, Xiaoyun

    2018-04-01

    The morphology-controlled synthesis of nano-structure photocatalyst have leaded a new possibility to improve their physical and chemical properties. Herein, Bi2WO6 nanocrystals (BWO) with nano-flower, nano plates, knot shape, rod like and irregular morphologies have been successfully synthesized through a highly facile hydrothermal process by simply adjusting pH values, reactive solvents and temperature. Photocatalytic activity of the as-prepared samples were evaluated by degradation of Ceftriaxone sodium under visible light irradiation (λ > 420 nm), the results indicated that all the BWO samples exhibit morphology-associated photocatalytic activity, and the 3D flowerlike-structure of BWO composed of well-ordered nano plates (BWO-D-5) displayed the outstanding photocatalytic activity. Through getting insight into the mechanism, h+ and rad O2- play major roles compared with rad OH in photocatalytic degradation process. The possible pathway of Ceftriaxone sodium and the intermediates were proposed to better understand the reaction process. Moreover, this work not only provides an example of morphology-dependent photocatalytic activity of BWO but also provides an illustrative example for removing organic pollutant molecules according to practical requirements.

  5. Synthesis of metal free ultrathin graphitic carbon nitride sheet for photocatalytic dye degradation of Rhodamine B under visible light irradiation

    Science.gov (United States)

    Rahman, Shakeelur; Momin, Bilal; Higgins M., W.; Annapure, Uday S.; Jha, Neetu

    2018-04-01

    In recent times, low cost and metal free photocatalyts driven under visible light have attracted a lot of interest. One such photo catalyst researched extensively is bulk graphitic carbon nitride sheets. But the low surface area and weak mobility of photo generated electrons limits its photocatalytic performance in the visible light spectrum. Here we present the facile synthesis of ultrathin graphitic carbon nitride using a cost effective melamine precursor and its application in highly efficient photocatalytic dye degradation of Rhodamine B molecules. Compared to bulk graphitic carbon nitride, the synthesized ultrathin graphitic carbon nitride shows an increase in surface area, a a decrease in optical band gap and effective photogenerated charge separation which facilitates the harvest of visible light irradiation. Due to these optimal properties of ultrathin graphitic carbon nitride, it shows excellent photocatalytic activity with photocatalytic degradation of about 95% rhodamine B molecules in 1 hour.

  6. Fuel assembly

    International Nuclear Information System (INIS)

    Hirukawa, Koji; Sakurada, Koichi.

    1992-01-01

    In a fuel assembly for a BWR type reactor, water rods or water crosses are disposed between fuel rods, and a value with a spring is disposed at the top of the coolant flow channel thereof, which opens a discharge port when pressure is increased to greater than a predetermined value. Further, a control element for the amount of coolant flow rate is inserted retractable to a control element guide tube formed at the lower portion of the water rod or the water cross. When the amount of control elements inserted to the control element guide tube is small and the inflown coolant flow rate is great, the void coefficient at the inside of the water rod is less than 5%. On the other hand, when the control elements are inserted, the flow resistance is increased, so that the void coefficient in the water rod is greater than 80%. When the pressure in the water rod is increased, the valve with the spring is raised to escape water or steams. Then, since the variation range of the change of the void coefficient can be controlled reliably by the amount of the control elements inserted, and nuclear fuel materials can be utilized effectively. (N.H.)

  7. Fabricated CeO2 nanopowders as a novel sensing platform for advanced forensic, electrochemical and photocatalytic applications

    Science.gov (United States)

    Rohini, B. S.; Nagabhushana, H.; Darshan, G. P.; Basavaraj, R. B.; Sharma, S. C.; Sudarmani, R.

    2017-11-01

    In Forensic investigation, identification of various types of ridge details are essential in order to fix the criminals associated in various crimes. Even though several methods and labeling agents are available to visualize latent finger prints (LFPs) there is still simple, accurate, cost-effective, and non-destructive tool is required. In the present work, CeO2 nanopowders (NPs) are prepared via simple solution combustion route using Tamarindus indica fruit extract as a fuel. The optimized NPs are utilized for visualization of LFPs on various surfaces by powder dusting method. Results revealed that visualized LFPs exhibit Level 3 features such as pores and ridge contours under normal light with high sensitivity and without background hindrance. The photometric characteristics of the prepared samples exhibit blue color emission and highly useful in warm light emitting diodes. The photocatalytic studies were carried out with different Methylene blue (MB) dye concentration and pH values. The obtained results reveal that the CeO2 NPs exhibits an excellent catalytic properties which can act as a good catalytic reagent. The findings demonstrate that the prepared NPs are quite useful as a labeling agent for visualization of LFPs, efficient catalysts for dye degradation as well as solid-state lighting applications.

  8. A CsPbBr3 Perovskite Quantum Dot/Graphene Oxide Composite for Photocatalytic CO2 Reduction.

    Science.gov (United States)

    Xu, Yang-Fan; Yang, Mu-Zi; Chen, Bai-Xue; Wang, Xu-Dong; Chen, Hong-Yan; Kuang, Dai-Bin; Su, Cheng-Yong

    2017-04-26

    Halide perovskite quantum dots (QDs), primarily regarded as optoelectronic materials for LED and photovoltaic devices, have not been applied for photochemical conversion (e.g., water splitting or CO 2 reduction) applications because of their insufficient stability in the presence of moisture or polar solvents. Herein, we report the use of CsPbBr 3 QDs as novel photocatalysts to convert CO 2 into solar fuels in nonaqueous media. Under AM 1.5G simulated illumination, the CsPbBr 3 QDs steadily generated and injected electrons into CO 2 , catalyzing CO 2 reduction at a rate of 23.7 μmol/g h with a selectivity over 99.3%. Additionally, through the construction of a CsPbBr 3 QD/graphene oxide (CsPbBr 3 QD/GO) composite, the rate of electron consumption increased 25.5% because of improved electron extraction and transport. This study is anticipated to provide new opportunities to utilize halide perovskite QD materials in photocatalytic applications.

  9. Solid TRU fuels and fuel cycle technology

    International Nuclear Information System (INIS)

    Ogawa, Toru; Suzuki, Yasufumi

    1997-01-01

    Alloys and nitrides are candidate solid fuels for transmutation. However, the nitride fuels are preferred to the alloys because they have more favorable thermal properties which allows to apply a cold-fuel concept. The nitride fuel cycle technology is briefly presented

  10. Used fuel packing plant for CANDU fuel

    Energy Technology Data Exchange (ETDEWEB)

    Menzies, I.; Thayer, B.; Bains, N., E-mail: imenzies@atsautomation.com [ATS Automation, Cambridge, ON (Canada); Murchison, A., E-mail: amurchison@nwmo.ca [NWMO, Toronto, ON (Canada)

    2015-07-01

    Large forgings have been selected to containerize Light Water Reactor used nuclear fuel. CANDU fuel, which is significantly smaller in size, allows novel approaches for containerization. For example, by utilizing commercially available extruded ASME pipe a conceptual design of a Used Fuel Packing Plant for containerization of used CANDU fuel in a long lived metallic container has been developed. The design adopts a modular approach with multiple independent work cells to transfer and containerize the used fuel. Based on current technologies and concepts from proven industrial systems, the Used Fuel Packing Plant can assemble twelve used fuel containers per day considering conservative levels of process availability. (author)

  11. A facile synthesis of nanorods of ZnO/graphene oxide composites with enhanced photocatalytic activity

    International Nuclear Information System (INIS)

    Qin, Jiaqian; Zhang, Xinyu; Xue, Yannan; Kittiwattanothai, Nutsakun; Kongsittikul, Pongsakorn; Rodthongkum, Nadnudda; Limpanart, Sarintorn; Ma, Mingzhen; Liu, Riping

    2014-01-01

    Graphical abstract: - Highlights: • Room temperature method to prepare ZnO–GO composites. • ZnO–GO composites exhibit superior absorption ability and photocatalytic performance. • With GO content increasing, the absorption and photocatalytic ability increased. - Abstract: Graphene oxide (GO)–ZnO nanorods composites were successfully synthesized by a facile room-temperature approach using the colloidal coagulation effect. The samples are characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, specific surface area, and UV–vis spectroscopy. The photodegradation of methylene blue (MB) has been investigated in the presence of composites. It is observed that the absorption capacity and photocatalytic effect could be enhanced by adding graphene oxide

  12. Mesoporous cerium oxide nanospheres for the visible-light driven photocatalytic degradation of dyes

    Directory of Open Access Journals (Sweden)

    Subas K. Muduli

    2014-04-01

    Full Text Available A facile, solvothermal synthesis of mesoporous cerium oxide nanospheres is reported for the purpose of the photocatalytic degradation of organic dyes and future applications in sustainable energy research. The earth-abundant, relatively affordable, mixed valence cerium oxide sample, which consists of predominantly Ce7O12, has been characterized by powder X-ray diffraction, X-ray photoelectron and UV–vis spectroscopy, and transmission electron microscopy. Together with N2 sorption experiments, the data confirms that the new cerium oxide material is mesoporous and absorbs visible light. The photocatalytic degradation of rhodamin B is investigated with a series of radical scavengers, suggesting that the mechanism of photocatalytic activity under visible-light irradiation involves predominantly hydroxyl radicals as the active species.

  13. Preparation and Characterization of Surface Photocatalytic Activity with NiO/TiO2 Nanocomposite Structure

    Directory of Open Access Journals (Sweden)

    Jian-Zhi Chen

    2015-07-01

    Full Text Available This study achieved a nanocomposite structure of nickel oxide (NiO/titanium dioxide (TiO2 heterojunction on a TiO2 film surface. The photocatalytic activity of this structure evaluated by decomposing methylene blue (MB solution was strongly correlated to the conductive behavior of the NiO film. A p-type NiO film of high concentration in contact with the native n-type TiO2 film, which resulted in a strong inner electrical field to effectively separate the photogenerated electron-hole pairs, exhibited a much better photocatalytic activity than the controlled TiO2 film. In addition, the photocatalytic activity of the NiO/TiO2 nanocomposite structure was enhanced as the thickness of the p-NiO film decreased, which was beneficial for the migration of the photogenerated carriers to the structural surface.

  14. Room temperature synthesis and enhanced photocatalytic property of CeO2/ZnO heterostructures

    Science.gov (United States)

    Wang, Chao; Fan, Huiqing; Ren, Xiaohu; Fang, Jiawen

    2018-02-01

    To achieve better photocatalytic performance, we proposed a facile solid-state reaction method to produce CeO2/ZnO heterostructures. Ceria and zinc oxide were synthesized simultaneously by thoroughly grinding the mixture of zinc acetate dihydrate, cerium nitrate hexahydrate and sodium hydroxide. The morphology of the as-prepared heterostructures varies dramatically as different amount of ceria was introduced in the composition. The photocatalytic performance of CeO2/ZnO heterojunctions was 4.6 times higher than that of pure ZnO. The enhanced photocatalytic activity could be ascribed to that more electrons and holes could transport to the surface of catalysts and react with the pollution due to the extended light-responsive range, accelerated migration, increased specific surface area and suppressed recombination of photogenerated carriers.

  15. Preparation and Characterization of Surface Photocatalytic Activity with NiO/TiO₂ Nanocomposite Structure.

    Science.gov (United States)

    Chen, Jian-Zhi; Chen, Tai-Hong; Lai, Li-Wen; Li, Pei-Yu; Liu, Hua-Wen; Hong, Yi-You; Liu, Day-Shan

    2015-07-13

    This study achieved a nanocomposite structure of nickel oxide (NiO)/titanium dioxide (TiO₂) heterojunction on a TiO₂ film surface. The photocatalytic activity of this structure evaluated by decomposing methylene blue (MB) solution was strongly correlated to the conductive behavior of the NiO film. A p -type NiO film of high concentration in contact with the native n -type TiO₂ film, which resulted in a strong inner electrical field to effectively separate the photogenerated electron-hole pairs, exhibited a much better photocatalytic activity than the controlled TiO₂ film. In addition, the photocatalytic activity of the NiO/TiO₂ nanocomposite structure was enhanced as the thickness of the p -NiO film decreased, which was beneficial for the migration of the photogenerated carriers to the structural surface.

  16. Study of the Photocatalytic Property of Polysulfone Membrane Incorporating TiO2 Nanoparticles

    Science.gov (United States)

    Chen, Xingxing; Zhou, Weiqi; Chen, Zhe; Yao, Lei

    In order to investigate the effect of the incorporated nanoparticles on the photocatalytic property of the hybrid membranes, the uncovered and covered polysulfone/TiO2 hybrid membranes were prepared. Positron annihilation γ-ray spectroscopy coupled with a positron beam was utilized to examine the depth profiles of the two membranes. The photocatalytic activities of the membranes were evaluated by the degradation of Rhodamine B (RhB) aqueous solution under the irradiation of Xe lamp. UV-Vis spectroscopy was applied to study the UV transmission through the polysulfone layer. Electrochemical impedance spectroscopy was used to detect the photo-generated charges by the covered membrane during the irradiation. It can be found that UV light can penetrate through the covered layer (about 230nm), and the incorporated nanoparticles can still generate charges under irradiation, which endows the photocatalytic ability of the covered membrane.

  17. Preparation of powders Ag3PO4 and study of their photocatalytic activity

    International Nuclear Information System (INIS)

    Badurova, K.

    2014-01-01

    In our thesis we dealt with preparing powders of Ag 3 PO 4 by using Na 2 HPO 4 ·12H 2 O and Na 3 PO 4 ·12H 2 O as two different precursors. Samples were prepared by precipitation and mechanochemical methods. Photocatalytic efficiency of individual samples was studied by irradiation of suspensions of prepared powders with methylene blue (MB) solution and with phenol solution using source of light similar to solar light. Photocatalytic efficiency was determined via method of determination of total organic carbon (TOC) as the time dependence of phenol concentration and also via monitoring spectrophotometric parameters of solution as the time dependence of MB solution colouring intensity. Effect of sample preparation method on photocatalytic efficiency and morphology of particles was studied. After that, samples were characterised by X-ray powder diffraction method (XRD), scanning electron microscopy (SEM) and Raman spectroscopy (authors)

  18. Synthesis of ZnO/CdSe hierarchical heterostructure with improved visible photocatalytic efficiency

    International Nuclear Information System (INIS)

    Wu, Yao; Xu, Fang; Guo, Defu; Gao, Zhiyong; Wu, Dapeng; Jiang, Kai

    2013-01-01

    ZnO/CdSe hierarchical heterostructure was prepared using pompon-like ZnO as substrate materials, and hexagonal CdSe nanoparticles were dispersed on the ZnO plates. The hybrid ZnO/CdSe samples were intensively investigated by XRD, SEM, TEM, HRTEM, PL and UV–vis absorption spectrum. The photocatalytic experiments confirm that ZnO/CdSe heterostructure exhibits improved photocatalytic efficiency compared to pure ZnO under visible light irradiation. CdSe nanoparticles are believed to serve as photosensitizers to extend the absorption spectrum to visible light region. In addition, the incorporation of CdSe can suppress the recombination of photogenerated electron-hole pairs, which contributes to the enhancement of photocatalytic efficiency.

  19. Effect of amorphous fluorinated coatings on photocatalytic properties of anodized titanium surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Persico, Federico [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali, Via G. Giusti, 9, 50121 Firenze (Italy); Sansotera, Maurizio, E-mail: maurizio.sansotera@polimi.it [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali, Via G. Giusti, 9, 50121 Firenze (Italy); Diamanti, Maria Vittoria [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Magagnin, Luca; Venturini, Francesco; Navarrini, Walter [Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131, Milano (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali, Via G. Giusti, 9, 50121 Firenze (Italy)

    2013-10-31

    The photocatalytic activity promoted by anodized titanium surfaces coated with different amorphous perfluoropolymers was evaluated. A copolymer between tetrafluoroethylene and perfluoro-4-trifluoromethoxy-1,3-dioxole and two perfluoropolyethers containing ammonium phosphate and triethoxysilane functionalities, respectively, were tested as coating materials. These coatings revealed good adhesion to the anodized titanium substrate and conferred to it both hydrophobicity and oleophobicity. The photocatalytic activity of the coating on anodized titanium was evaluated by monitoring the degradation of stearic acid via Infrared spectroscopy. The degradation rate of stearic acid was reduced but not set to zero by the presence of the fluorinated coatings, leading to the development of advanced functional coatings. The morphological variations of the coatings as a result of photocatalysis were also determined by atomic force microscopy. - Highlights: • Coated anodized titanium surfaces show a decreased wettability. • Evaluation of the stability of perfluorinated coatings towards photocatalysis. • Amorphous perfluorinated coatings do not hinder photocatalytic activity.

  20. Photocatalytic activity of sonochemically prepared TiO_2 decorated with silver nanoparticles

    International Nuclear Information System (INIS)

    Michal, R.

    2017-01-01

    A novel way of titanium dioxide synthesis using non-water environment was investigated. In synthesis, water causes aggregation of particles of titania thus reducing active surface significantly. To avoid this, a non- water environment such as toluene was employed. Reaction between solid precursor and gaseous ammonia was conducted in this environment using dried reactants in tempered glass reactor and irradiated by ultrasonic horn. As prepared powders were then calcinated and decorated with Ag nanoparticles. Photocatalytic activity was determined by TOC method and compared to P25 standard TiO_2. Samples were analysed by XRD and Raman spectroscopy and surface morphology was investigated by SEM. Powders prepared by this method had comparable or higher photocatalytic activity than P25. Ag nanoparticles seem to have no significant impact on photocatalytic activity whatsoever. (authors)

  1. Reduced graphene oxide is not a universal promoter for photocatalytic activities of TiO2

    Directory of Open Access Journals (Sweden)

    Hui Ling Tan

    2017-03-01

    Full Text Available Addition of reduced graphene oxide (RGO to P25 TiO2 was made and its impacts on photocatalytic oxidation of various organic substances were studied. Although the presence of RGO in TiO2 can enhance certain TiO2-based photocatalytic reactions, it is not a universal observation that can be expected in all types of organic substances. The factor of photocatalytic activity enhancement is strongly affected by the various functional groups appeared in the organic substances. In this work, it is realised that the length of alkyl chain in alcohols and carboxylic acids have the minimum influence on the overall activity while the number of hydroxyl groups can promote the further activity enhancement in the presence of RGO.

  2. Titanium dioxide encapsulation of supported Ag nanoparticles on the porous silica bead for increased photocatalytic activity

    Science.gov (United States)

    Liu, Hui; Deng, Lu; Sun, Chaochao; Li, Junqi; Zhu, Zhenfeng

    2015-01-01

    A new synthetic strategy has been developed to encapsulate Ag nanoparticles in heterogeneous catalysts to prevent their dropping and sintering. Ag nanoparticles with diameters about 5-10 nm were first supported on the porous silica bead. These were then covered with a fresh layer of titanium dioxide with the thickness about 5 nm. SEM and TEM images were used to confirm the success of each synthesis step, and the photocatalytic activity of the as-synthesized samples was evaluated by photocatalytic decolorization of Rhodamine B (Rh B) aqueous solution at ambient temperature under both UV and visible light irradiation. The resulting titanium dioxide encapsulated Ag nanoparticles exhibited an enhanced photocatalytic activity under both UV and visible light irradiation, this can be attributed to effective charge separation and light harvesting of the plasmonic silver nanoparticles decoration, even the reducing of the exciton recombination rate caused by the small grain size of anatase TiO2 nanocrystals.

  3. Photocatalytic Solar Tower Reactor for the Elimination of a Low Concentration of VOCs

    Directory of Open Access Journals (Sweden)

    Nobuaki Negishi

    2014-10-01

    Full Text Available We developed a photocatalytic solar tower reactor for the elimination of low concentrations of volatile organic compounds (VOCs typically emitted from small industrial establishments. The photocatalytic system can be installed in a narrow space, as the reactor is cylindrical-shaped. The photocatalytic reactor was placed vertically in the center of a cylindrical scattering mirror, and this vertical reactor was irradiated with scattered sunlight generated by the scattering mirror. About 5 ppm toluene vapor, used as representative VOC, was continuously photodegraded and converted to CO2 almost stoichiometrically under sunny conditions. Toluene removal depended only on the intensity of sunlight. The performance of the solar tower reactor did not decrease with half a year of operation, and the average toluene removal was 36% within this period.

  4. Preparation, Characterization, and Photocatalytic Activity of TiO2/ZnO Nanocomposites

    Directory of Open Access Journals (Sweden)

    Liqin Wang

    2013-01-01

    Full Text Available Nanoparticles of the TiO2/ZnO composite photocatalysts were prepared via sol-gel process. The crystalline structure, morphology, thermal stability, and pore structure properties of the composite photocatalysts were characterized by XRD, FE-SEM, TG-DTA, and N2 physical adsorption measurements. The photocatalytic activity of the composite catalysts was evaluated by photocatalytic degradation reaction of methyl orange (MO in aqueous solution. The best preparation parameters for the composite photocatalysts were obtained through systematical experiments. Furthermore, the photocatalytic degradation reaction of aqueous MO solution followed the first-order reaction kinetics; the relative equation can be described as ln(C0/C=0.5689t, and the calculated correlation constant (R2 is 0.9937 for the calibration curve.

  5. Synthesis and Photocatalytic Activity of Anatase TiO2 Nanoparticles-coated Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Xie Yi

    2009-01-01

    Full Text Available Abstract A simple and straightforward approach to prepare TiO2-coated carbon nanotubes (CNTs is presented. Anatase TiO2 nanoparticles (NPs with the average size ~8 nm were coated on CNTs from peroxo titanic acid (PTA precursor even at low temperature of 100 °C. We demonstrate the effects of CNTs/TiO2 molar ratio on the adsorption capability and photocatalytic efficiency under UV–visible irradiation. The samples showed not only good optical absorption in visible range, but also great adsorption capacity for methyl orange (MO dye molecules. These properties facilitated the great enhancement of photocatalytic activity of TiO2 NPs-coated CNTs photocatalysts. The TiO2 NPs-coated CNTs exhibited 2.45 times higher photocatalytic activity for MO degradation than that of pure TiO2.

  6. Investigation of photocatalytic activity of titanium dioxide deposited on metallic substrates by DC magnetron sputtering

    DEFF Research Database (Denmark)

    Daviðsdóttir, Svava; Canulescu, Stela; Dirscherl, Kai

    2013-01-01

    The photocatalytic properties of titanium dioxide (TiO2) coating in the anatase crystalline structure deposited on aluminium AA1050 alloy and stainless steel S316L substrates were investigated. The coating was prepared by DC magnetron sputtering. The microstructure and surface morphology of the c......The photocatalytic properties of titanium dioxide (TiO2) coating in the anatase crystalline structure deposited on aluminium AA1050 alloy and stainless steel S316L substrates were investigated. The coating was prepared by DC magnetron sputtering. The microstructure and surface morphology...... sweep voltammetry, impedance measurements. The microstructure and surface morphology of the coating were similar irrespective of the nature of the substrate, while the photocatalytic behaviour was found to vary depending on the substrate type. In general the TiO2 coating on stainless steel was shown...

  7. Photocatalytic degradation of selected herbicides in aqueous suspensions of doped titania under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Sojic, Daniela V., E-mail: daniela.sojic@dh.uns.ac.rs [Department of Chemistry, Biochemistry and Environmental Protection, Faculty of Sciences, University of Novi Sad, Trg D. Obradovica 3, 21000 Novi Sad (Serbia); Despotovic, Vesna N., E-mail: vesna.despotovic@dh.uns.ac.rs [Department of Chemistry, Biochemistry and Environmental Protection, Faculty of Sciences, University of Novi Sad, Trg D. Obradovica 3, 21000 Novi Sad (Serbia); Abazovic, Nadica D., E-mail: kiki@vinca.rs [Vinca Institute of Nuclear Sciences, 11001 Beograd, PO Box 522 (Serbia); Comor, Mirjana I., E-mail: mirjanac@vinca.rs [Vinca Institute of Nuclear Sciences, 11001 Beograd, PO Box 522 (Serbia); Abramovic, Biljana F., E-mail: biljana.abramovic@dh.uns.ac.rs [Department of Chemistry, Biochemistry and Environmental Protection, Faculty of Sciences, University of Novi Sad, Trg D. Obradovica 3, 21000 Novi Sad (Serbia)

    2010-07-15

    The aim of this work was to study the efficiency of Fe- and N-doped titania suspensions in the photocatalytic degradation of the herbicides RS-2-(4-chloro-o-tolyloxy)propionic acid (mecoprop, MCPP), (4-chloro-2-methylphenoxy)acetic acid (MCPA), and 3,6-dichloropyridine-2-carboxylic acid (clopyralid, CP) under the visible light ({lambda} {>=} 400 nm) irradiation. The obtained results were compared with those of the corresponding undoped TiO{sub 2} (rutile/anatase) and of the most frequently used TiO{sub 2} Degussa P25. Computational modeling procedures were used to optimize geometry and molecular electrostatic potentials of MCPP, MCPA and CP and discuss the obtained results. The results indicate that the efficiency of photocatalytic degradation is greatly influenced by the molecular structure of the compound. Lowering of the band gap of titanium dioxide by doping is not always favorable for increasing photocatalytic efficiency of degradation.

  8. Preparation and Photocatalytic Performance of Bamboo-Charcoal-Supported Nano-ZnO Composites

    Directory of Open Access Journals (Sweden)

    Yunlong ZHOU

    2018-02-01

    Full Text Available Nano-ZnO/bamboo charcoal composites were prepared by precipitation with bamboo charcoal as support. Nano-ZnO/bamboo charcoal composites were characterized by XRD, SEM and EDS. Photocatalytic degradation processes of methyl orange were studied. The results indicate that the structure of nano-ZnO is of the wurtzite type and the grain size is about 19-54 nm. The best preparation temperature for these composites is 500℃. The composites have better photocatalytic degradation ability than pure ZnO under UV irradiation. Photocatalytic degradation of methyl orange with the composites obeys first-order kinetics, and the composites can be recycled.DOI: http://dx.doi.org/10.5755/j01.ms.24.1.17397

  9. Solar Light Responsive Photocatalytic Activity of Reduced Graphene Oxide-Zinc Selenide Nanocomposite

    Science.gov (United States)

    Chakraborty, Koushik; Ibrahim, Sk; Das, Poulomi; Ghosh, Surajit; Pal, Tanusri

    2017-10-01

    Solution processable reduced graphene oxide-zinc selenide (RGO-ZnSe) nanocomposite has been successfully synthesized by an easy one-pot single-step solvothermal reaction. The RGO-ZnSe composite was characterized structurally and morphologically by the study of XRD analysis, SEM and TEM imaging. Reduction in graphene oxide was confirmed by FTIR spectroscopy analysis. Photocatalytic efficiency of RGO-ZnSe composite was investigated toward the degradation of Rhodamine B under solar light irradiation. Our study indicates that the RGO-ZnSe composite is catalytically more active compared to the controlled-ZnSe under the solar light illumination. Here, RGO plays an important role for photoinduced charge separation and subsequently hinders the electron-hole recombination probability that consequently enhances photocatalytic degradation efficiency. We expect that this type of RGO-based optoelectronics materials opens up a new avenue in the field of photocatalytic degradation of different organic water pollutants.

  10. Photocatalytic degradation of indigo carmine by ZnO photocatalyst under visible light irradiation

    Directory of Open Access Journals (Sweden)

    Ali Al- Taie

    2017-09-01

    Full Text Available In this work, the photocatalytic degradation of indigo carmine (IC using zinc oxide suspension was studied. The effect of influential parameters such as initial indigo carmine concentration and catalyst loading were studied with the effect of Vis irradiation in the presence of reused ZnO was also investigated. The increased in initial dye concentration decreased the photodegradation and the increased catalyst loading increased the degradation percentage and the reused-ZnO exhibits lower photocatalytic activity than the ZnO catalyst. It has been found that the photocatalytic degradation of indigo carmine obeyed the pseudo-first-order kinetic reaction in presence of zinc oxide. This was found from plotting the relationship between ln (C0/Ct and irradiation the rate constant of the process.UV- spectrophotometer was used to study the indigo carmine photodegradation

  11. Photocatalytic sterilization of TiO2 films coated on Al fiber

    International Nuclear Information System (INIS)

    Luo Li; Miao Lei; Tanemura, Sakae; Tanemura, Masaki

    2008-01-01

    Photocatalytic TiO 2 films were coated on Al fiber by sol-gel dip-coating method, and then annealed. The crystal structure and morphology of the films were performed by XRD, TEM and SEM. Photocatalytic sterilization of the films was investigated in O 2 atmosphere through purifying the aqueous solution with facultative aerobe (Bacillus cereus), aerobe (Pseudomonas aeruginosa) and anaerobe (Staphylococcus aureus, Enterococcus faecalis and Escherichia coli). In the presence of O 2 , it benefits to generate O 2 · - and ·OH at the first stage of the photocatalytic reaction, while the excess O 2 restrains the anaerobe from reproducing and accelerates the reproducing for the aerobe at the second stage of reaction. As a result, it was found that the crystal of TiO 2 films is anatase phase and the films have excellent sterilization effect against facultative aerobe and anaerobe. Nevertheless, it only decreased the bioactivity against aerobe in a short time

  12. Enhancing Photocatalytic Degradation of Methyl Blue Using PVP-Capped and Uncapped CdSe Nanoparticles

    Directory of Open Access Journals (Sweden)

    Kgobudi Frans Chepape

    2017-01-01

    Full Text Available Quantum confinement of semiconductor nanoparticles is a potential feature which can be interesting for photocatalysis, and cadmium selenide is one simple type of quantum dot to use in the following photocatalytic degradation of organic dyes. CdSe nanoparticles capped with polyvinylpyrrolidone (PVP in various concentration ratios were synthesized by the chemical reduction method and characterized. The transmission electron microscopy (TEM analysis of the samples showed that 50% PVP-capped CdSe nanoparticles were uniformly distributed in size with an average of 2.7 nm and shape which was spherical-like. The photocatalytic degradation of methyl blue (MB in water showed efficiencies of 31% and 48% when using uncapped and 50% PVP-capped CdSe nanoparticles as photocatalysts, respectively. The efficiency of PVP-capped CdSe nanoparticles indicated that a complete green process can be utilized for photocatalytic treatment of water and waste water.

  13. Application of Titanium Dioxide-Graphene Composite Material for Photocatalytic Degradation of Alkylphenols

    Directory of Open Access Journals (Sweden)

    Chanbasha Basheer

    2013-01-01

    Full Text Available Titanium dioxide-graphene (TiO2-G composite was used for the photodegradation of alkylphenols in wastewater samples. The TiO2-G composites were prepared via sonochemical and calcination methods. The synthesized composite was characterized by X-ray diffraction (XRD, infrared spectroscopy (IR, scanning electron microscopy (SEM, transmission electron microscopy (TEM, energy dispersive X-ray analysis (EDX, and fluorescence spectroscopy. The photocatalytic efficiency was evaluated by studying the degradation profiles of alkylphenols using gas chromatography-flame ionization detector (GC-FID. It was found that the synthesized TiO2-G composites exhibit enhanced photocatalytic efficiencies as compared to pristine TiO2. The presence of graphene not only provides a large surface area support for the TiO2 photocatalyst, but also stabilizes charge separation by trapping electrons transferred from TiO2, thereby hindering charge transfer and enhancing its photocatalytic efficiency.

  14. Starch mediated CdS nanoparticles and their photocatalytic performance under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Firdaus, Farha, E-mail: Farha-firdaus@yahoo.co.in [Chemistry Section, Women’s College, Aligarh Muslim University, Aligarh 202002 UP (India); Faraz, Mohd [Department of Chemistry, Faculty of Science, Aligarh Muslim University, Aligarh 202002 (India)

    2016-05-06

    Green synthesis of Cadmium Sulphide (CdS-S) nanoparticles is of considerable interest due to its biocompatible and nontoxicity. Here, we present a biomolecule stimulated chemical method was adopted for the successful synthesis of CdS-S nanoparticles using starch as a capping agent. The CdS-S nanoparticles were characterized by various analytical techniques. The CdS-S nanoparicles exhibit photocatalytic activity against methyl orange (MO) at pH 9 in Visible light and the reaction follows pseudo first-order kinetics. The comparative photocatalytic activity revealed that CdS-S nanoparticles remarkably enhanced activities as compared to the commercial TiO{sub 2} nanoparticles. The outcome of these studies offers valuable for planning CdS-S nanoparticles having photocatalytic activities helpful for the formulation of waste water remediation.

  15. Titanium-Phosphonate-Based Metal-Organic Frameworks with Hierarchical Porosity for Enhanced Photocatalytic Hydrogen Evolution

    KAUST Repository

    Li, Hui

    2018-02-01

    Photocatalytic hydrogen production is crucial for solar-to-chemical conversion process, wherein high-efficiency photocatalysts lie in the heart of this area. Herein a new photocatalyst of hierarchically mesoporous titanium-phosphonate-based metal-organic frameworks, featuring well-structured spheres, periodic mesostructure and large secondary mesoporosity, are rationally designed with the complex of polyelectrolyte and cathodic surfactant serving as the template. The well-structured hierarchical porosity and homogeneously incorporated phosphonate groups can favor the mass transfer and strong optical absorption during the photocatalytic reactions. Correspondingly, the titanium phosphonates exhibit significantly improved photocatalytic hydrogen evolution rate along with impressive stability. This work can provide more insights into designing advanced photocatalysts for energy conversion and render a tunable platform in photoelectrochemical field.

  16. Core/shell structured ZnO/SiO2 nanoparticles: Preparation, characterization and photocatalytic property

    International Nuclear Information System (INIS)

    Zhai Jing; Tao Xia; Pu Yuan; Zeng Xiaofei; Chen Jianfeng

    2010-01-01

    ZnO nanoparticles were prepared by a simple chemical synthesis route. Subsequently, SiO 2 layers were successfully coated onto the surface of ZnO nanoparticles to modify the photocatalytic activity in acidic or alkaline solutions. The obtained particles were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectrometry (EDS) and zeta potential. It was found that ultrafine core/shell structured ZnO/SiO 2 nanoparticles were successfully obtained. The photocatalytic performance of ZnO/SiO 2 core/shell structured nanoparticles in Rhodamine B aqueous solution at varied pH value were also investigated. Compared with uncoated ZnO nanoparticles, core/shell structured ZnO/SiO 2 nanoparticles with thinner SiO 2 shell possess improved stability and relatively better photocatalytic activity in acidic or alkaline solutions, which would broaden its potential application in pollutant treatment.

  17. Preparation of self-cleaning surfaces with a dual functionality of superhydrophobicity and photocatalytic activity

    Science.gov (United States)

    Park, Eun Ji; Yoon, Hye Soo; Kim, Dae Han; Kim, Yong Ho; Kim, Young Dok

    2014-11-01

    Thin film of polydimethylsiloxane (PDMS) was deposited on SiO2 nanoparticles by chemical vapor deposition, and SiO2 became completely hydrophobic after PDMS coating. Mixtures of TiO2 and PDMS-coated SiO2 nanoparticles with various relative ratios were prepared, and distributed on glass surfaces, and water contact angles and photocatalytic activities of these surfaces were studied. Samples consisting of TiO2 and PDMS-coated SiO2 with a ratio of 7:3 showed a highly stable superhydrophobicity under UV irradiation with a water contact angle of 165° and UV-driven photocatalytic activity for decomposition of methylene blue and phenol in aqueous solution. Our process can be exploited for fabricating self-cleaning surfaces with dual functionality of superhydrophobicity and photocatalytic activity at the same time.

  18. Photocatalytic mineralisation of aniline derivatives in aquatic systems using semiconductor oxides.

    Science.gov (United States)

    Habibi, Mohammad Hossein; Khaledisardashti, Mohammad; Montazerozohori, Morteza

    2004-01-01

    Photocatalytic degradation of aqueous solution of aniline derivatives such as ortho-nitroaniline (ONA), meta-nitroaniline (MNA), para-nitroaniline (PNA), 4-bromoaniline (4-BrA) and 2-chloroaniline (2-ClA) were carried out over ZnO or TiO2 (anatase and rutile) in a photocatalytic reactor. The observed results revealed that the order of photocatalytic activity for degradation of selected compound was ZnO > TiO2 (rutile) > TiO2 (anatase) with the ratio of the rate constants to the surface area of 3.2 x 10(-3), 1.9 x 10(-3) and 1.0 x 10(-3) respectively. The effect of some physical and chemical parameters such as amount of photocatalyst, pH, time of irradiation and solvent were studied. Degradation kinetic was according to Longmuir behaviour. Spectrophotometric methods and TOC analysis supported that aniline derivatives almost completely mineralized.

  19. Starch mediated CdS nanoparticles and their photocatalytic performance under visible light irradiation

    International Nuclear Information System (INIS)

    Firdaus, Farha; Faraz, Mohd

    2016-01-01

    Green synthesis of Cadmium Sulphide (CdS-S) nanoparticles is of considerable interest due to its biocompatible and nontoxicity. Here, we present a biomolecule stimulated chemical method was adopted for the successful synthesis of CdS-S nanoparticles using starch as a capping agent. The CdS-S nanoparticles were characterized by various analytical techniques. The CdS-S nanoparicles exhibit photocatalytic activity against methyl orange (MO) at pH 9 in Visible light and the reaction follows pseudo first-order kinetics. The comparative photocatalytic activity revealed that CdS-S nanoparticles remarkably enhanced activities as compared to the commercial TiO 2 nanoparticles. The outcome of these studies offers valuable for planning CdS-S nanoparticles having photocatalytic activities helpful for the formulation of waste water remediation.

  20. Titanium-Phosphonate-Based Metal-Organic Frameworks with Hierarchical Porosity for Enhanced Photocatalytic Hydrogen Evolution

    KAUST Repository

    Li, Hui; Sun, Ying; Yuan, Zhong-Yong; Zhu, Yun-Pei; Ma, Tianyi

    2018-01-01

    Photocatalytic hydrogen production is crucial for solar-to-chemical conversion process, wherein high-efficiency photocatalysts lie in the heart of this area. Herein a new photocatalyst of hierarchically mesoporous titanium-phosphonate-based metal-organic frameworks, featuring well-structured spheres, periodic mesostructure and large secondary mesoporosity, are rationally designed with the complex of polyelectrolyte and cathodic surfactant serving as the template. The well-structured hierarchical porosity and homogeneously incorporated phosphonate groups can favor the mass transfer and strong optical absorption during the photocatalytic reactions. Correspondingly, the titanium phosphonates exhibit significantly improved photocatalytic hydrogen evolution rate along with impressive stability. This work can provide more insights into designing advanced photocatalysts for energy conversion and render a tunable platform in photoelectrochemical field.

  1. AgBr/diatomite for the efficient visible-light-driven photocatalytic degradation of Rhodamine B

    Science.gov (United States)

    Fang, Jing; Zhao, Huamei; Liu, Qinglei; Zhang, Wang; Gu, Jiajun; Su, Yishi; Abbas, Waseem; Su, Huilan; You, Zhengwei; Zhang, Di

    2018-03-01

    The treatment of organic pollution via photocatalysis has been investigated for a few decades. However, earth-abundant, cheap, stable, and efficient substrates are still to be developed. Here, we prepare an efficient visible-light-driven photocatalyst via the deposition of Ag nanoparticles (light intensity. For comparison, AgBr/SiO2 ( κ = 0.04 min-1) and commercial AgBr nanoparticles ( κ = 0.05 min-1) were measured as well. The experimental results reveal that diatomite acted more than a substrate benefiting the dispersion of AgBr nanoparticles, as well as a cooperator to help harvest visible light and adsorb dye molecules, leading to the efficient visible-light-driven photocatalytic performance of AgBr/diatomite. Considering the low cost (10 per ton) and large-scale availability of diatomite, our study provides the possibility to prepare other types of diatomite-based efficient photocatalytic composites with low-cost but excellent photocatalytic performance.

  2. Synthesis, characterization and photocatalytic performance of chemically exfoliated MoS2

    Science.gov (United States)

    Prabhakar Vattikuti, S. V.; Shim, Jaesool

    2018-03-01

    Two-dimensional (2D) layered structure transition metal dichalcogenides (TMDs) has gained huge attention and importance for photocatalytic energy conversion because of their unique properties. Molybdenum disulfide (MoS2) nanosheets were synthesized via one-pot method and exfoliated in (dimethylformamide) DMF solution. Subsequent exfoliated MoS2 nanosheets (e-MoS2) were used as photocatalysts for degradation of Rhodamine B (RhB) pollutant under solar light irradiation. The e-MoS2 nanosheets exhibited excellent photocatalytic activity than that of pristine MoS2, owing to high specific surface area with enormous active sites and light absorption capacity. In addition, e-MoS2 demonstrated remarkable photocatalytic stability.

  3. Obtaining carbon nanotubes/ZnO for use in the photocatalytic organic pollutants

    International Nuclear Information System (INIS)

    Dalt, S. da; Pulcinelli, N.O.; Bergmann, C.P.

    2016-01-01

    This study aims to obtain nanocomposites of carbon nanotubes (CNTs) with nanostructured zinc oxide (ZnO), and characterize the samples as its structure and photocatalytic activity, for their application in the degradation of organic pollutants, in the case organic dye methyl orange. The nanocomposites were obtained from commercial NTC (Baytubes®), commercial ZnO, produced by Merck and ZnO obtained from the synthesis by combustion. The NTC-ZnO nanocomposites were prepared in solution from the physical mixture of materials, and subsequently analyzed structurally and investigated for their photocatalytic activity, employing them as catalysts in degradation of the dye in aqueous solution under ultraviolet radiation. Samples were analyzed by X-ray diffraction and specific surface area (BET). The photocatalytic performance of nanocomposites can be correlated to the phase found and the surface area measured. (author)

  4. Photocatalytic activity and interfacial carrier transfer of Ag-TiO2 nanoparticle films

    International Nuclear Information System (INIS)

    Xin Baifu; Ren Zhiyu; Hu Haiyuan; Zhang Xiangyu; Dong Chunlei; Shi Keying; Jing Liqiang; Fu Honggang

    2005-01-01

    The electrodes of Ag-TiO 2 with different Ag content are prepared by a modified sol-gel method. The photochemical properties of Ag-TiO 2 with different Ag content are characterized by surface photovoltage spectroscopy (SPS). The results show that the SPS intensity decreased with increasing Ag contents. This demonstrates that the doping Ag plays the roles trapping photoinduced electrons, which inhibiting the recombination of photoinduced electrons and holes. The photoelectrochemical properties of Ag-TiO 2 electrodes with different Ag content are performed by electrochemical impedance spectroscopy (EIS) under high-pressure mercury lamp (160 W) illuminating, and photocatalytic degradation of RhB are studied at the same time. The experimental results indicate that the process of charge transfer is a controlled-step of photocatalytic reaction. The SPS intensity and the electrical impedance values of EIS equivalent circuits are contrary to photocatalytic degradation ratio of RhB

  5. Nuclear fuel preheating system

    International Nuclear Information System (INIS)

    Andrea, C.

    1975-01-01

    A nuclear reactor new fuel handling system which conveys new fuel from a fuel preparation room into the reactor containment boundary is described. The handling system is provided with a fuel preheating station which is adaptd to heat the new fuel to reactor refueling temperatures in such a way that the fuel is heated from the top down so that fuel element cladding failure due to thermal expansions is avoided. (U.S.)

  6. Fuel element loading system

    International Nuclear Information System (INIS)

    Arya, S.P; s.

    1978-01-01

    A nuclear fuel element loading system is described which conveys a plurality of fuel rods to longitudinal passages in fuel elements. Conveyor means successively position the fuel rods above the longitudinal passages in axial alignment therewith and adapter means guide the fuel rods from the conveyor means into the longitudinal passages. The fuel elements are vibrated to cause the fuel rods to fall into the longitudinal passages through the adapter means

  7. Photocatalytic effects for the TiO2-coated phosphor materials

    International Nuclear Information System (INIS)

    Yoon, Jin-Ho; Jung, Sang-Chul; Kim, Jung-Sik

    2011-01-01

    Research highlights: → The photocatalytic behavior of the coupling of TiO 2 with phosphorescent materials. → The photobleaching of an MB aqueous solution under visible light irradiation. → The ALD TiO 2 -coated phosphor composite showed much higher photocatalytic reactivity. → The light emitted from the phosphors contributed to the photo-generation. - Abstract: This study investigated the photocatalytic behavior of the coupling of TiO 2 with phosphorescent materials. A TiO 2 thin film was deposited on CaAl 2 O 4 :Eu 2+ ,Nd 3+ phosphor particles by using atomic layer deposition (ALD), and its photocatalytic reaction was investigated by the photobleaching of an aqueous solution of methylene-blue (MB) under visible light irradiation. To clarify the mechanism of the TiO 2 -phosphorescent materials, two different samples of TiO 2 -coated phosphor and TiO 2 -Al 2 O 3 -coated phosphor particles were prepared. The photocatalytic mechanisms of the ALD TiO 2 -coated phosphor powders were different from those of the pure TiO 2 and TiO 2 -Al 2 O 3 -coated phosphor. The absorbance in a solution of the ALD TiO 2 -coated phosphor decreased much faster than that of pure TiO 2 under visible irradiation. In addition, the ALD TiO 2 -coated phosphor showed moderately higher photocatalytic degradation of MB solution than the TiO 2 -Al 2 O 3 -coated phosphor did. The TiO 2 -coated phosphorescent materials were characterized by transmission electron microscopy (TEM), Auger electron spectroscopy (AES) and X-ray photon spectroscopy (XPS).

  8. Unravelling the pH-dependence of a molecular photocatalytic system for hydrogen production.

    Science.gov (United States)

    Reynal, Anna; Pastor, Ernest; Gross, Manuela A; Selim, Shababa; Reisner, Erwin; Durrant, James R

    2015-08-01

    Photocatalytic systems for the reduction of aqueous protons are strongly pH-dependent, but the origin of this dependency is still not fully understood. We have studied the effect of different degrees of acidity on the electron transfer dynamics and catalysis taking place in a homogeneous photocatalytic system composed of a phosphonated ruthenium tris(bipyridine) dye ( RuP ) and a nickel bis(diphosphine) electrocatalyst ( NiP ) in an aqueous ascorbic acid solution. Our approach is based on transient absorption spectroscopy studies of the efficiency of photo-reduction of RuP and NiP correlated with pH-dependent photocatalytic H 2 production and the degree of catalyst protonation. The influence of these factors results in an observed optimum photoactivity at pH 4.5 for the RuP - NiP system. The electron transfer from photo-reduced RuP to NiP is efficient and independent of the pH value of the medium. At pH RuP photo-reduction by the sacrificial electron donor, ascorbic acid. At pH >4.5, the efficiency of the system is limited by the poor protonation of NiP , which inhibits its ability to reduce protons to hydrogen. We have therefore developed a rational strategy utilising transient absorption spectroscopy combined with bulk pH titration, electrocatalytic and photocatalytic experiments to disentangle the complex pH-dependent activity of the homogenous RuP - NiP photocatalytic system, which can be widely applied to other photocatalytic systems.

  9. Treatment of secondary effluent by sequential combination of photocatalytic oxidation with ceramic membrane filtration.

    Science.gov (United States)

    Song, Lili; Zhu, Bo; Jegatheesan, Veeriah; Gray, Stephen; Duke, Mikel; Muthukumaran, Shobha

    2018-02-01

    The aim of the present work was to experimentally evaluate an alternative advanced wastewater treatment system, which combines the action of photocatalytic oxidation with ceramic membrane filtration. Experiments were carried out using laboratory scale TiO 2 /UV photocatalytic reactor and tubular ceramic microfiltration (CMF) system to treat the secondary effluent (SE). A 100-nm pore size CMF membrane was investigated in cross flow mode under constant transmembrane pressure of 20 kPa. The results show that specific flux decline of CMF membrane with and without TiO 2 /UV photocatalytic treatment was 30 and 50%, respectively, after 60 min of filtration. Data evaluation revealed that the adsorption of organic compounds onto the TiO 2 particles was dependent on the pH of the suspension and was considerably higher at low pH. The liquid chromatography-organic carbon detector (LC-OCD) technique was used to characterise the dissolved organic matter (DOM) present in the SE and was monitored following photocatalysis and CMF. The results showed that there was no removal of biopolymers and slight removal of humics, building blocks and the other oxidation by-products after TiO 2 /UV photocatalytic treatment. This result suggested that the various ions present in the SE act as scavengers, which considerably decrease the efficiency of the photocatalytic oxidation reactions. On the other hand, the CMF was effective for removing 50% of biopolymers with no further removal of other organic components after photocatalytic treatment. Thus, the quantity of biopolymers in SE has an apparent correlation with the filterability of water samples in CMF.

  10. Ultrasonic synthesis of fern-like ZnO nanoleaves and their enhanced photocatalytic activity

    International Nuclear Information System (INIS)

    Ma, Qing Lan; Xiong, Rui; Zhai, Bao-gai; Huang, Yuan Ming

    2015-01-01

    Graphical abstract: - Highlights: • Fern-like ZnO nanoleaves were synthesized by ultrasonicating Zn microcrystals in water. • A fern-like ZnO nanoleaf is a self-assembly of ZnO nanoplates along one ZnO nanorod. • Fern-like ZnO nanoleaves exhibit enhanced photocatalytic activity than ZnO nanocrystals. • The branched hierarchical structures are responsible for the enhanced photocatalytic activity. - Abstract: Two-dimensional fern-like ZnO nanoleaves were synthesized by ultrasonicating zinc microcrystals in water. The morphology, crystal structure, optical property and photocatalytic activity of the fern-like ZnO nanoleaves were characterized with scanning electron microscopy, X-ray diffraction, transmission electron microscopy, photoluminescence spectroscopy and ultraviolet–visible spectroscopy, respectively. It is found that one fern-like ZnO nanoleaf is composed of one ZnO nanorod as the central trunk and a number of ZnO nanoplates as the side branches in opposite pairs along the central ZnO nanorod. The central ZnO nanorod in the fern-like nanoleaves is about 1 μm long while the side-branching ZnO nanoplates are about 100 nm long and 20 nm wide. Further analysis has revealed that ZnO nanocrystals are the building blocks of the central ZnO nanorod and the side-branching ZnO nanoplates. Under identical conditions, fern-like ZnO nanoleaves exhibit higher photocatalytic activity in photodegrading methyl orange in aqueous solution than spherical ZnO nanocrystals. The first-order photocatalytic rate constant of the fern-like ZnO nanoleaves is about four times as large as that of the ZnO nanoparticles. The branched architecture of the hierarchical nanoleaves is suggested be responsible for the enhanced photocatalytic activity of the fern-like ZnO nanoleaves

  11. Artificial fuel

    Energy Technology Data Exchange (ETDEWEB)

    Hamon, L L.W.

    1918-08-20

    Lignite, peat, sud, leaf-mold, or shale, or two or more of these raw carbonaceous materials are mixed with cellulose material, such as sawdust, silica, alkali, and tar or pitch, or residues from tar or pitch, or residues from the distillation of oils, and the mixture is molded into blocks. Other carbonaceous materials, such as graphite, anthracite, or coal-dust, coke, breeze, or culm, and mineral substances, such as iron and manganese ores, may be added. A smokeless fuel can be obtained by coking the blocks in the usual way in retorts.

  12. Photocatalytic degradation of paracetamol: intermediates and total reaction mechanism.

    Science.gov (United States)

    Moctezuma, Edgar; Leyva, Elisa; Aguilar, Claudia A; Luna, Raúl A; Montalvo, Carlos

    2012-12-01

    The advanced oxidation of paracetamol (PAM) promoted by TiO(2)/UV system in aqueous medium was investigated. Monitoring this reaction by HPLC and TOC, it was demonstrated that while oxidation of paracetamol is quite efficient under these conditions, its mineralization is not complete. HPLC indicated the formation of hydroquinone, benzoquinone, p-aminophenol and p-nitrophenol in the reaction mixtures. Further evidence of p-nitrophenol formation was obtained following the reaction by UV-vis spectroscopy. Continuous monitoring by IR spectroscopy demonstrated the breaking of the aromatic amide present in PAM and subsequent formation of several aromatic intermediate compounds such as p-aminophenol and p-nitrophenol. These aromatic compounds were eventually converted into trans-unsaturated carboxylic acids. Based on these experimental results, an alternative deacylation mechanism for the photocatalytic oxidation of paracetamol is proposed. Our studies also demonstrated IR spectroscopy to be a useful technique to investigate oxidative mechanisms of pharmaceutical compounds. Copyright © 2012 Elsevier B.V. All rights reserved.

  13. Toward designing semiconductor-semiconductor heterojunctions for photocatalytic applications

    Science.gov (United States)

    Zhang, Liping; Jaroniec, Mietek

    2018-02-01

    Semiconductor photocatalysts show a great potential for environmental and energy-related applications, however one of the major disadvantages is their relatively low photocatalytic performance due to the recombination of electron-hole pairs. Therefore, intensive research is being conducted toward design of heterojunctions, which have been shown to be effective for improving the charge-transfer properties and efficiency of photocatalysts. According to the type of band alignment and direction of internal electric field, heterojunctions are categorized into five different types, each of which is associated with its own charge transfer characteristics. Since the design of heterojunctions requires the knowledge of band edge positions of component semiconductors, the commonly used techniques for the assessment of band edge positions are reviewed. Among them the electronegativity-based calculation method is applied for a large number of popular visible-light-active semiconductors, including some widely investigated bismuth-containing semiconductors. On basis of the calculated band edge positions and the type of component semiconductors reported, heterojunctions composed of the selected bismuth-containing semiconductors are proposed. Finally, the most popular synthetic techniques for the fabrication of heterojunctions are briefly discussed.

  14. Photocatalytic Treatment of Shower Water Using a Pilot Scale Reactor

    Directory of Open Access Journals (Sweden)

    Yash Boyjoo

    2012-01-01

    Full Text Available Treatment of shower water deserves special consideration for reuse not only because of its low pollutant loading but also because it is produced in large quantities. In this study, a pilot scale study of photocatalytic degradation of impurities in real shower water was performed in a 31 L volume reactor using titanium dioxide as the photocatalyst. The reactor was operated in a continuous slurry recirculation mode. Several operational parameters were studied including the slurry initial pH, catalyst concentration, air flow rate, and slurry recirculation rate. Up to 57% of total organic carbon (TOC elimination was obtained after 6 hours of treatment (for 3.0 slurry initial pH, 0.07 gL−1 catalyst concentration, 1.8 Lmin−1 air flow rate, and 4.4 Lmin−1 slurry recirculation rate. This study showed that photocatalysis could be successfully transposed from bench scale to pilot scale. Furthermore, the ease of operation and the potential to use solar energy make photocatalysis an attractive prospect with respect to treatment of grey water.

  15. Synthesis and Characterization of Metal Phosphates for Photocatalytic Applications

    KAUST Repository

    Al-Sabban, Bedour

    2012-07-01

    Solar energy is the most abundant efficient and important source of renewable energy. The objective of this study is to develop highly efficient visible light responsive photocatalysts for overall water splitting. This is done by using silver or copper containing materials. Phosphate compounds have caught much attention due to their rigid structure, thermal stability and resistance to chemical attacks. Solid phosphates can be prepared by direct solid-state reaction between metal cations and phosphate anions at high temperatures. Double metal phosphates of the Nasion-type structure had shown further technological importance. It has been reported that well-crystallized double metal phosphate particles have excellent ordering and cationic conduction channels in the Nasicon framework. In this study, several Nasion-type structured materials have been synthesized by solid-state method (e.g. CuTi2(PO4)3 and AgTi2(PO4)3) heated up under different temperatures (400–1100C) in N2 or air atmosphere. These materials were characterized by XRD, SEM, DR-UV-Vis spectroscopy and tested for photocatalytic applications. A new method for direct synthesis of photoelectrode on Ti Plate had been demonstrated. Further investigations on controlling the size and morphology for better performance of single and double metal phosphates will be done.

  16. Photocatalytic decolorization of methyl orange dye using nano-photocatalysts

    Directory of Open Access Journals (Sweden)

    amin ahmadpour

    2015-10-01

    Full Text Available Environmental contamination, which is growing around the world, is a serious problem can not to be neglected. Among all contaminations, water pollution is a major problem. Azo dyes are one of the largest groups of pollutants found in the drinking water, coming from, and the food and textile industries. TiO2/Fe3O4 and TiO2/Fe2O3 nanocomposites with various ratios were synthesized by an ultrasonic-assisted deposition-precipitation method and their UV-light decolorization of methyl orange (MO dye was investigated. The effect of Fe3O4/TiO2 and Fe2O3-TiO2 nanocomposites ratio on the photocatalytic activity and magnetic property of the nanocomposites was studied by comparing their decolorization curves and magnetism in the presence of magnet, respectively. The results revealed that the decolorization efficiency of 1 wt% Fe3O4/TiO2 nanocomposite reached about 40% within 60 min UV irradiation at room temperature. However, this sample showed the least magnetism. Also, the ability of synthesized nanocomposites in holding the adsorbed methyl orange dye on their surface and the effect of pH were investigated.

  17. Integral Design Methodology of Photocatalytic Reactors for Air Pollution Remediation

    Directory of Open Access Journals (Sweden)

    Claudio Passalía

    2017-06-01

    Full Text Available An integral reactor design methodology was developed to address the optimal design of photocatalytic wall reactors to be used in air pollution control. For a target pollutant to be eliminated from an air stream, the proposed methodology is initiated with a mechanistic derived reaction rate. The determination of intrinsic kinetic parameters is associated with the use of a simple geometry laboratory scale reactor, operation under kinetic control and a uniform incident radiation flux, which allows computing the local superficial rate of photon absorption. Thus, a simple model can describe the mass balance and a solution may be obtained. The kinetic parameters may be estimated by the combination of the mathematical model and the experimental results. The validated intrinsic kinetics obtained may be directly used in the scaling-up of any reactor configuration and size. The bench scale reactor may require the use of complex computational software to obtain the fields of velocity, radiation absorption and species concentration. The complete methodology was successfully applied to the elimination of airborne formaldehyde. The kinetic parameters were determined in a flat plate reactor, whilst a bench scale corrugated wall reactor was used to illustrate the scaling-up methodology. In addition, an optimal folding angle of the corrugated reactor was found using computational fluid dynamics tools.

  18. Structures and photocatalytic behavior of tantalum-oxynitride thin films

    International Nuclear Information System (INIS)

    Hsieh, J.H.; Li, Chuan; Liang, H.C.

    2011-01-01

    Tantalum oxynitride films were created by direct nitridation/oxidation during rapid thermal annealing at temperatures 450-700 deg. C. Instead of during deposition, this post process may be proved to be an alternative way to make transition metallic oxynitride films. With sufficient supply of oxygen flow (≥ 30 sccm), TaO x N y was formed as examined from X-ray diffraction (XRD) analysis. This oxynitride film has a broad optical absorption over the range of visible light and sufficient photocatalytic function. For optical absorption, the films' transmittance and reflectance were measured by a UV-VIS-NIR spectrophotometer with wavelengths ranging from 300 to 900 nm. The broad visible light absorption is associated with the formation of band gap in TaO x N y film, which was examined by the theoretical calculations combining the Beer-Lambert law and Tauc formula. Lastly, the photocatalysis of TaO x N y was gauged by the photodegradation test which measured the reduction of light absorbance affected by the decomposition of methylene blue (C 16 H 18 N 3 SCl.3H 2 O) on TaO x N y under visible light irradiation.

  19. Enhanced photocatalytic activity of SrTiO3 photocatalyst by topotactic preparation

    Science.gov (United States)

    Cao, Jiafeng; Huang, Xianshan; Liu, Yi; Wu, Jianguang; Ji, Yuexia

    2016-11-01

    Novel SrTiO3 (ST) photocatalysts with different shapes such as plates, rods and cubes were successfully synthesized based on a topotactic approach. The rod-like ST particles formed in situ at the plates show superior photocatalytic activities towards the decomposition of Rhodamine B than the plate-like and the cubic particles under visible-light irradiation, which could be attributed to the crystal orientation exposing highly active sites accompanied by the crystallite growth in molten salt. The results reveal an effective approach for fabrication of novel photocatalysts of perovskite structure with enhanced photocatalytic activities.

  20. Isolation, Characterization, and Environmental Application of Bio-Based Materials as Auxiliaries in Photocatalytic Processes

    Directory of Open Access Journals (Sweden)

    Davide Palma

    2018-05-01

    Full Text Available Sustainable alternative substrates for advanced applications represent an increasing field of research that attracts the attention of worldwide experts (in accordance with green chemistry principles. In this context, bio-based substances (BBS isolated from urban composted biowaste were purified and characterized. Additionally, these materials were tested as auxiliaries in advanced oxidizing photocatalytic processes for the abatement of organic contaminants in aqueous medium. Results highlighted the capability of these substances to enhance efficiency in water remediation treatments under mild conditions, favoring the entire light-driven photocatalytic process.

  1. Facile Solvothermal Synthesis of BiOCl/ZnO Heterostructures with Enhanced Photocatalytic Activity

    Directory of Open Access Journals (Sweden)

    Yong-Fang Li

    2014-01-01

    Full Text Available Well-defined nanosheet-assembled (BiOClx(ZnO1−x nanoflowers were synthesized by a solvothermal method. It was found that ZnO nanoparticles were anchored on the flower-like BiOCl nanostructures, as demonstrated by varying the initial compositions of the Bi precursor and the volume ratios of mixed solvents (ethylene glycol to water. The as-prepared (BiOCl0.6(ZnO0.4 nanocomposites showed enhanced photocatalytic activity toward rhodamine B degradation under ultraviolet (UV irradiation. And the photocatalytic mechanism was discussed in detail.

  2. Synthesis and photocatalytic activity of TiO2/conjugated polymer complex nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Shi Xiong Min; Fang Wang; Lei Feng; Yong Chun Tong; Zi Rong Yang

    2008-01-01

    A photocatalyst of nanometer TiO2/conjugated polymer complex was successfully synthesized and characterized by spectroscopic methods and photocatalytic experiments. The complex photocatalyst could be activated by absorbing both ultraviolet and visible light (λ=190-800nm). Methylene blue (MB) could be degraded more efficiently on the complex photocatalyst than on the TiO2 under natural light. The conjugated polymer played a promoting role in the photocatalytic degradation of MB. The calcination temperature had an important effect in degradation of dye and could be summarized as 260℃>300℃>340℃>220℃>180℃.

  3. Synthesis and photocatalytic properties of Sn-doped TiO{sub 2} nanotube arrays

    Energy Technology Data Exchange (ETDEWEB)

    Tu Yafang; Huang Shengyou [Department of Physics, Wuhan University, Wuhan 430072 (China); Sang Jianping, E-mail: jpsang@acc-lab.whu.edu.c [Department of Physics, Wuhan University, Wuhan 430072 (China); Department of Physics, Jianghan University, Wuhan 430056 (China); Zou Xianwu [Department of Physics, Wuhan University, Wuhan 430072 (China)

    2009-08-12

    TiO{sub 2} nanotube arrays doped by Sn up to 12 at% have been prepared using template-based liquid phase deposition method. Their morphologies, structures and optical properties have been investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, UV-vis absorption spectroscopy and photoluminescence spectroscopy. The photocatalytic properties of the samples were evaluated with the degradation of methylene blue under UV irradiation. The result shows that doping an appropriate amount of Sn can effectively improve the photocatalytic activity of TiO{sub 2} nanotube arrays, and the optimum dopant amount is found to be 5.6 at% in our experiments.

  4. Defective TiO2 with oxygen vacancies: synthesis, properties and photocatalytic applications

    Science.gov (United States)

    Pan, Xiaoyang; Yang, Min-Quan; Fu, Xianzhi; Zhang, Nan; Xu, Yi-Jun

    2013-04-01

    Titanium dioxide (TiO2), as an important semiconductor metal oxide, has been widely investigated in the field of photocatalysis. The properties of TiO2, including its light absorption, charge transport and surface adsorption, are closely related to its defect disorder, which in turn plays a significant role in the photocatalytic performance of TiO2. Among all the defects identified in TiO2, oxygen vacancy is one of the most important and is supposed to be the prevalent defect in many metal oxides, which has been widely investigated both by theoretical calculations and experimental characterizations. Here, we give a short review on the existing strategies for the synthesis of defective TiO2 with oxygen vacancies, and the defect related properties of TiO2 including structural, electronic, optical, dissociative adsorption and reductive properties, which are intimately related to the photocatalytic performance of TiO2. In particular, photocatalytic applications with regard to defective TiO2 are outlined. In addition, we offer some perspectives on the challenge and new direction for future research in this field. We hope that this tutorial minireview would provide some useful contribution to the future design and fabrication of defective semiconductor-based nanomaterials for diverse photocatalytic applications.Titanium dioxide (TiO2), as an important semiconductor metal oxide, has been widely investigated in the field of photocatalysis. The properties of TiO2, including its light absorption, charge transport and surface adsorption, are closely related to its defect disorder, which in turn plays a significant role in the photocatalytic performance of TiO2. Among all the defects identified in TiO2, oxygen vacancy is one of the most important and is supposed to be the prevalent defect in many metal oxides, which has been widely investigated both by theoretical calculations and experimental characterizations. Here, we give a short review on the existing strategies for the

  5. Preparation of sensitized ZnS and its photocatalytic activity under visible light irradiation

    International Nuclear Information System (INIS)

    Zhang Haitao; Chen Xinyi; Li Zhaosheng; Kou Jiahui; Yu Tao; Zou Zhigang

    2007-01-01

    In this paper, sensitized ZnS with visible light driven photocatlytic ability was successfully prepared. The obtained ZnS was characterized by x-ray diffraction, UV-visible diffuse reflectance spectra and Fourier transform infrared spectra. The photocatalytic property of the prepared ZnS was evaluated by decomposing methyl orange (MO). These sensitized ZnS powders with a proper molar ratio showed higher photocatalytic activity than TiO 2 (P25) under visible light (λ > 420 nm) irradiation. A possible explanation for the visible light activity of the prepared ZnS was proposed

  6. Photocatalytic action of cerium molybdate and iron-titanium oxide hollow nanospheres on Escherichia coli

    Energy Technology Data Exchange (ETDEWEB)

    Kartsonakis, I. A., E-mail: ikartsonakis@ims.demokritos.gr; Kontogiani, P.; Pappas, G. S.; Kordas, G. [NCSR ' DEMOKRITOS' , Sol-Gel Laboratory, Institute of Advanced Materials, Physicochemical Processes, Nanotechnology and Microsystems (Greece)

    2013-06-15

    This study is focused on the production of hollow nanospheres that reveal antibacterial action. Cerium molybdate and iron-titanium oxide hollow nanospheres with a diameter of 175 {+-} 15 and 221 {+-} 10 nm, respectively, were synthesized using emulsion polymerization and the sol-gel process. Their morphology characterization was accomplished using scanning electron microscopy. Their antibacterial action was examined on pure culture of Escherichia coli considering the loss of their viability. Both hollow nanospheres presented photocatalytic action after illumination with blue-black light, but those of cerium molybdate also demonstrated photocatalytic action in the dark. Therefore, the produced nanospheres can be used for antibacterial applications.

  7. Photocatalytic action of cerium molybdate and iron-titanium oxide hollow nanospheres on Escherichia coli

    International Nuclear Information System (INIS)

    Kartsonakis, I. A.; Kontogiani, P.; Pappas, G. S.; Kordas, G.

    2013-01-01

    This study is focused on the production of hollow nanospheres that reveal antibacterial action. Cerium molybdate and iron-titanium oxide hollow nanospheres with a diameter of 175 ± 15 and 221 ± 10 nm, respectively, were synthesized using emulsion polymerization and the sol–gel process. Their morphology characterization was accomplished using scanning electron microscopy. Their antibacterial action was examined on pure culture of Escherichia coli considering the loss of their viability. Both hollow nanospheres presented photocatalytic action after illumination with blue–black light, but those of cerium molybdate also demonstrated photocatalytic action in the dark. Therefore, the produced nanospheres can be used for antibacterial applications.

  8. Preparation and photocatalytic activity of B, Y co-doped nanosized TiO_2 catalyst

    Institute of Scientific and Technical Information of China (English)

    石中亮; 刘富梅; 姚淑华

    2010-01-01

    The catalysts of un-doped, single-doped and co-doped titanium dioxide (TiO2) powders were prepared by sol-gel method with Ti(OC4H9)4 as a raw material. The photocatalytic decomposition of phenol in aqueous solution under UV light was used as a probe reaction to evaluate their photocatalytic activities. The effects of B, Y co-doping on the crystallite sizes, crystal pattern, surface composition, and optical property of the catalyst were investigated by thermogravimetric differential thermal analysis, X-ray d...

  9. Antibacterial and photocatalytic degradation efficacy of silver nanoparticles biosynthesized using Cordia dichotoma leaf extract

    Science.gov (United States)

    Mankamna Kumari, R.; Thapa, Nikita; Gupta, Nidhi; Kumar, Ajeet; Nimesh, Surendra

    2016-12-01

    The present study focuses on the biosynthesis of silver nanoparticles (AgNPs) along with its antibacterial and photocatalytic activity. The AgNPs were synthesized using Cordia dichotoma leaf extract and were characterized using UV-vis spectroscopy to determine the formation of AgNPs. FTIR was done to discern biomolecules responsible for reduction and capping of the synthesized nanoparticles. Further, DLS technique was performed to examine its hydrodynamic diameter, followed by SEM, TEM and XRD to determine its size, morphology and crystalline structure. Later, these AgNPs were studied for their potential role in antibacterial activity and photocatalytic degradation of azo dyes such as methylene blue and Congo red.

  10. Photocatalytic transformation of dyes and by-products in the presence of hydrogen peroxide.

    Science.gov (United States)

    Subba Rao, K V; Subrahmanyam, M; Boule, P

    2003-08-01

    The efficiency of the photocatalytic degradation of dyes and dyeing industry pollutants on immobilized photocatalysts can be improved by addition of hydrogen peroxide, due to its photocatalytic decomposition on TiO2. Experiments were carried out with two azodyes, Acid Orange-7 (AO-7) and Tartrazine (Tart), with 3-nitrobenzenesulfonic add (3-NBSA) which is a chemical intermediate in the dye industry and with real industrial wastewaters, using a thin-film fixed bed reactor. The effect of hydrogen peroxide is only significant for concentrations higher than 5 x 10(-3) M (170 mg l(-1)).

  11. Porous-ZnO-Nanobelt Film as Recyclable Photocatalysts with Enhanced Photocatalytic Activity

    Directory of Open Access Journals (Sweden)

    Wang Min

    2010-01-01

    Full Text Available Abstract In this article, the porous-ZnO-nanobelt film was synthesized by oxidizing the ZnSe-nanobelt film in air. The experiment results show that the porous-ZnO-nanobelt film possesses enhanced photocatalytic activity compared with the ZnO-nanobelt film, and can be used as recyclable photocatalysts. The enhanced photocatalytic activity of the porous-ZnO-nanobelt film is attributed to the increased surface area. Therefore, turning the 1D-nanostructure film into porous one may be a feasible approach to meet the demand of photocatalyst application.

  12. Solar photocatalytic mineralization of isoproturon over TiO{sub 2}/HY composite systems

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Mangalampalli V. Phanikrishna; Lalitha, Kannekanti; Durgakumari, Valluri; Subrahmanyam, Machiraju [Inorganic and Physical Chemistry Division, Indian Institute of Chemical Technology, Hyderabad 500007 (India)

    2008-03-15

    The present investigation covers immobilization of titanium dioxide over HY support for the treatment of isoproturon pesticide. Catalysts are characterized by XRD, SEM-EDAX, TEM, BET surface area and UV-vis DRS. A detailed photocatalytic degradation study under solar light in aqueous suspensions with parameters like loading of TiO{sub 2} over HY, amount of the catalyst, concentration of substrate, pH effect, durability of the catalyst and comparison between suspended TiO{sub 2} and supported systems are reported. Mineralization of isoproturon is monitored by total organic carbon, chemical oxygen demand and a plausible mechanism is proposed for photocatalytic degradation based on degradation products. (author)

  13. An Efficient Synthesis of 2-Substituted Benzimidazoles via Photocatalytic Condensation of o-Phenylenediamines and Aldehydes.

    Science.gov (United States)

    Kovvuri, Jeshma; Nagaraju, Burri; Kamal, Ahmed; Srivastava, Ajay K

    2016-10-10

    A photocatalytic method has been developed for the efficient synthesis of functionalized benzimidazoles. This protocol involves photocatalytic condensation of o-phenylenediamines with various aldehydes using the Rose Bengal as photocatalyst. The method was found to be general and was successfully employed for accessing pharmaceutically important benzimidazoles by the condensation of aromatic, heteroaromatic and aliphatic aldehydes with o-phenylenediamines, in good-to-excellent yields. Notably, the method was found to be effective for the condensation of less reactive heterocyclic aldehydes with o-phenylenediamines.

  14. Nuclear Fuel elements

    International Nuclear Information System (INIS)

    Hirakawa, Hiromasa.

    1979-01-01

    Purpose: To reduce the stress gradient resulted in the fuel can in fuel rods adapted to control the axial power distribution by the combination of fuel pellets having different linear power densities. Constitution: In a fuel rod comprising a first fuel pellet of a relatively low linear power density and a second fuel pellet of a relatively high linear power density, the second fuel pellet is cut at its both end faces by an amount corresponding to the heat expansion of the pellet due to the difference in the linear power density to the adjacent first fuel pellet. Thus, the second fuel pellet takes a smaller space than the first fuel pellet in the fuel can. This can reduce the stress produced in the portion of the fuel can corresponding to the boundary between the adjacent fuel pellets. (Kawakami, Y.)

  15. Fuel assembly

    International Nuclear Information System (INIS)

    Hiraiwa, Koji; Ueda, Makoto

    1989-01-01

    In a fuel assembly used for a light water cooled reactor such as a BWR type reactor, a water rod is divided axially into an upper outer tube and a lower outer tube by means of a plug disposed from the lower end of a water rod to a position 1/4 - 1/2 of the entire length for the water rod. Inlet apertures and exit apertures for moderators are respectively perforated for the divided outer tube and upper and lower portions. Further, an upper inner tube with less neutron irradiation growing amount than the outer tube is perforated on the plug in the outer tube, while a lower inner tube with greater neutron irradiation growing amount than the outer tube is suspended from the lower surface of the plug in the outer tube. Then, the opening area for the exit apertures disposed to the upper outer tube and the lower outer tube is controlled depending on the difference of the neutron irradiation growing amount between the upper inner tube and the upper outer tube, and the difference of the neutron irradiation growing amount between the lower inner tube and the lower outer tube. This enables effective spectral shift operation and improve the fuel economy. (T.M.)

  16. Fuel Burn Estimation Model

    Science.gov (United States)

    Chatterji, Gano

    2011-01-01

    Conclusions: Validated the fuel estimation procedure using flight test data. A good fuel model can be created if weight and fuel data are available. Error in assumed takeoff weight results in similar amount of error in the fuel estimate. Fuel estimation error bounds can be determined.

  17. Discussion on 'Solar detoxification of fuel-contaminated groundwater using fixed-bed photocatalysts'

    Energy Technology Data Exchange (ETDEWEB)

    Farrell, Joseph B.

    1997-03-15

    In a discussion of the 1997 paper by J. C. Crittenden et al. on the solar detoxification of fuel-contaminated groundwater using fixed-bed photocatalysts, the writer indicates a number of problems with the interpretation of the data and invites the authors to speculate on the reaction mechanism in the photocatalytic destruction of BTEX compounds in groundwater. In reply, Crittenden points out that it is not easy to speculate on the reaction mechanism because there are many compounds other than BTEX compounds contained in the water matrix, as well as many unknown compounds and by-products.

  18. Thermal evolution of structure and photocatalytic activity in polymer microsphere templated TiO{sub 2} microbowls

    Energy Technology Data Exchange (ETDEWEB)

    Erdogan, Deniz Altunoz; Polat, Meryem [Department of Chemistry, Bilkent University, 06800 Ankara (Turkey); Garifullin, Ruslan; Guler, Mustafa O. [Institute of Materials Science and Nanotechnology, National Nanotechnology Research Center (UNAM), Bilkent University, 06800 Ankara (Turkey); Ozensoy, Emrah, E-mail: ozensoy@fen.bilkent.edu.tr [Department of Chemistry, Bilkent University, 06800 Ankara (Turkey)

    2014-07-01

    Polystyrene cross-linked divinyl benzene (PS-co-DVB) microspheres were used as an organic template in order to synthesize photocatalytic TiO{sub 2} microspheres and microbowls. Photocatalytic activity of the microbowl surfaces were demonstrated both in the gas phase via photocatalytic NO(g) oxidation by O{sub 2}(g) as well as in the liquid phase via Rhodamine B degradation. Thermal degradation mechanism of the polymer template and its direct influence on the TiO{sub 2} crystal structure, surface morphology, composition, specific surface area and the gas/liquid phase photocatalytic activity data were discussed in detail. With increasing calcination temperatures, spherical polymer template first undergoes a glass transition, covering the TiO{sub 2} film, followed by the complete decomposition of the organic template to yield TiO{sub 2} exposed microbowl structures. TiO{sub 2} microbowl systems calcined at 600 °C yielded the highest per-site basis photocatalytic activity. Crystallographic and electronic properties of the TiO{sub 2} microsphere surfaces as well as their surface area play a crucial role in their ultimate photocatalytic activity. It was demonstrated that the polymer microsphere templated TiO{sub 2} photocatalysts presented in the current work offer a promising and a versatile synthetic platform for photocatalytic DeNO{sub x} applications for air purification technologies.

  19. Study of photocatalytic activities of Bi2WO6 nanoparticles synthesized by fast microwave-assisted method

    International Nuclear Information System (INIS)

    Phu, Nguyen Dang; Hoang, Luc Huy; Chen, Xiang-Bai; Kong, Meng-Hong; Wen, Hua-Chiang; Chou, Wu Ching

    2015-01-01

    We present a study of photocatalytic activities of Bi 2 WO 6 nanoparticles synthesized by fast microwave-assisted method. The photocatalytic activities of the nanoparticles were evaluated by the decolorization of methylene-blue under visible-light-irradiation. Our results show that the surface area of Bi 2 WO 6 nanoparticles plays a major role for improving photocatalytic activity, while visible-light absorption has only a weak effect on photocatalytic activity. This suggests efficient transportation of photo-generated electrons and holes to the oxidation active sites on the surface of nanoparticles, indicating Bi 2 WO 6 nanoparticles synthesized by fast microwave-assisted method are promising for achieving high photocatalytic activity under visible-light-irradiation. - Highlights: • The Bi 2 WO 6 nanoparticles were synthesized via fast microwave-assisted method. • The obtained Bi 2 WO 6 nanoparticles exhibited visible-light absorbance. • The surface area of Bi 2 WO 6 nanoparticles plays major role for improving photocatalytic activity. • The Bi 2 WO 6 nanoparticles are promising for achieving high photocatalytic activity under visible-light-irradiation

  20. Superhydrophobic photocatalytic PTFE – Titania coatings deposited by reactive pDC magnetron sputtering from a blended powder target

    Energy Technology Data Exchange (ETDEWEB)

    Ratova, Marina, E-mail: marina_ratova@hotmail.com; Kelly, Peter J.; West, Glen T.

    2017-04-01

    The production of photocatalytic coatings with superhydrophobic properties, as opposed to the conventional hydrophilic properties, is desirable for the prevention of adhesion of contaminants to photocatalytic surfaces with subsequent deterioration of photocatalytic properties. In this work polytetrafluoroethylene (PTFE) – TiO{sub 2} composite thin films were deposited using a novel method of reactive pulsed direct current (pDC) magnetron sputtering of a blended PTFE – titanium oxide powder target. The surface characteristics and photocatalytic properties of the deposited composite coatings were studied. The as-deposited coatings were annealed at 523 K in air and analysed with Raman spectroscopy, optical profilometry and scanning electron microscopy. Hydrophobicity was assessed though measurements of water contact angles, and photocatalytic properties were studied via methylene blue dye degradation under UV irradiation. It was found that variations of gas flow and, hence, process pressures allowed deposition of samples combining superhydrophobicity with stable photocatalytic efficiency under UV light irradiation. Reversible wettability behaviour was observed with the alternation of light-dark cycles. - Highlights: • PTFE-TiO{sub 2} coatings were deposited by pDC reactive magnetron sputtering. • Blended powder target was used for coatings deposition. • Deposited coatings combined superhydrophobic and photocatalytic properties. • Under UV irradiation coatings exhibited reversible wettability.

  1. Characterizations of nano-TiO{sub 2}/diatomite composites and their photocatalytic reduction of aqueous Cr (VI)

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Qing; Li, Hui; Zheng, Shuilin, E-mail: shuilinzh@sina.com; Sun, Zhiming, E-mail: szmcumtb@hotmail.com

    2014-08-30

    Graphical abstract: Nano-TiO{sub 2}/diatomite (DIA) composites were successfully synthesized by a typical hydrolysis precipitation method. The composites show good photocatalytic activity and stability for aqueous Cr (VI) removal. - Highlights: • TiO{sub 2} nanoparticles/diatomite composite was synthesized and characterized. • The composite exhibited a good photocatalytic performance in Cr (VI) reduction. • The photocatalyst showed good photocatalytic stability. • The composite is a promising material for Cr (VI) photocatalytic reduction. - Abstract: In this paper, the TiO{sub 2} nanoparticles were immobilized on diatomite (DIA) via a typical hydrolysis precipitation process using TiCl{sub 4} as precursor. The as-prepared composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). TiO{sub 2} nanoparticles with the average grain size of around 7–14 nm were well deposited on the surface of diatomite. The photocatalytic activity toward the reduction of aqueous Cr (VI) was demonstrated under UV light. The influence of initial pH values, catalyst amount, illumination intensity and initial concentration of Cr (VI) on photocatalytic reduction of Cr (VI) were investigated. Compared with the commercial TiO{sub 2} (P25, Degussa), the TiO{sub 2}/DIA composites had better reactive activity because of their relatively higher adsorption capacity. Furthermore, the prepared photocatalyst exhibited relatively good photocatalytic stability depending on the reusability tests.

  2. Constant strength fuel-fuel cell

    International Nuclear Information System (INIS)

    Vaseen, V.A.

    1980-01-01

    A fuel cell is an electrochemical apparatus composed of both a nonconsumable anode and cathode; and electrolyte, fuel oxidant and controls. This invention guarantees the constant transfer of hydrogen atoms and their respective electrons, thus a constant flow of power by submergence of the negative electrode in a constant strength hydrogen furnishing fuel; when said fuel is an aqueous absorbed hydrocarbon, such as and similar to ethanol or methnol. The objective is accomplished by recirculation of the liquid fuel, as depleted in the cell through specific type membranes which pass water molecules and reject the fuel molecules; thus concentrating them for recycle use

  3. Preparation, characterization and enhanced visible-light photocatalytic activities of BiPO4/BiVO4 composites

    International Nuclear Information System (INIS)

    Wu, Siyuan; Zheng, Hong; Lian, Youwei; Wu, Yiying

    2013-01-01

    Graphical abstract: - Highlights: • BiPO 4 /BiVO 4 composites were successfully prepared by the hydrothermal method. • BiPO 4 /BiVO 4 composites exhibited broad absorption in the visible region. • Visible-light photocatalytic activities of BiPO 4 /BiVO 4 composites were enhanced. • P/V molar ratio and pH value of the reaction affect photocatalytic activity. • The mechanism of enhanced visible-light photocatalytic activities was discussed. - Abstract: BiPO 4 /BiVO 4 composites with different P/V molar ratios were prepared by the hydrothermal method and the effect of pH values of hydrothermal reaction on photocatalytic activity of BiPO 4 /BiVO 4 composite was investigated. The photocatalysts were characterized by X-ray diffraction, field emission scanning electron microscopy, energy-dispersive spectroscopy, X-ray photoelectron spectroscopy and UV–vis diffuse reflectance spectroscopy. The photocatalytic property of BiPO 4 /BiVO 4 was evaluated by photocatalytic degradation of Methylene blue under visible light irradiation. The results showed that the photocatalytic activity of the composites was much higher than that of pure BiPO 4 and BiVO 4 . The rate constant of Methylene blue degradation over BiPO 4 /BiVO 4 (P/V molar ratio of 5:1 and hydrothermal reaction pH value of 1.5) is 1.7 times that of pure BiVO 4 . The photocatalytic activity enhancement of BiPO 4 /BiVO 4 composite is closely related to the BiVO 4 functioning as a sensitizer to adsorb visible light and the heterojunction of BiPO 4 /BiVO 4 acting as an active center for hindering the rapid recombination of electron–hole pairs during the photocatalytic reaction

  4. KMRR fuel design

    International Nuclear Information System (INIS)

    Son, D.S.; Sim, B.S.; Kim, T.R.; Hwang, W.; Kim, B.G.; Ku, Y.H.; Lee, C.B.; Lim, I.C.

    1992-06-01

    KMRR fuel rod design criteria on fuel swelling, blistering and oxide spallation have been reexamined. Fuel centerline temperature limit of 250deg C in normal operation condition and fuel swelling limit of 12 % at the end of life have been proposed to prevent fuel failure due to excessive fuel swelling. Fuel temperature limit of 485deg C has been proposed to exclude the possibility of fuel failures during transients or under accident condition. Further analyses are needed to decide the fuel cladding temperature limit to preclude the oxide spallation. Design changes in fuel assembly structure and their effects on related systems have been reviewed from a structural integrity viewpoint. The remained works in fuel mechanical design area have been identified and further efforts of fuel design group will be focused on these aspects. (Author)

  5. Fuel Property Blend Model

    Energy Technology Data Exchange (ETDEWEB)

    Pitz, William J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Mehl, Marco [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Wagnon, Scott J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Zhang, Kuiwen [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kukkadapu, Goutham [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Westbrook, Charles K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2017-01-12

    The object of this project is to develop chemical models and associated correlations to predict the blending behavior of bio-derived fuels when mixed with conventional fuels like gasoline and diesel fuels.

  6. Logistic Fuel Processor Development

    National Research Council Canada - National Science Library

    Salavani, Reza

    2004-01-01

    The Air Base Technologies Division of the Air Force Research Laboratory has developed a logistic fuel processor that removes the sulfur content of the fuel and in the process converts logistic fuel...

  7. Fuel pellet loading apparatus

    International Nuclear Information System (INIS)

    1980-01-01

    Apparatus is described for loading a predetermined amount of nuclear fuel pellets into nuclear fuel elements and particularly for the automatic loading of fuel pellets from within a sealed compartment. (author)

  8. Fuel assembly

    International Nuclear Information System (INIS)

    Wataumi, Kazutoshi; Tajiri, Hiroshi.

    1992-01-01

    In a fuel assembly of a BWR type reactor, a pellet to be loaded comprises an external layer of fissile materials containing burnable poisons and an internal layer of fissile materials not containing burnable poison. For example, there is provided a dual type pellet comprising an external layer made of UO 2 incorporated with Gd 2 O 3 at a predetermined concentration as the burnable poisons and an internal layer made of UO 2 not containing Gd 2 O 3 . The amount of the burnable poisons required for predetermined places is controlled by the thickness of the ring of the external layer. This can dissipate an unnecessary poisoning effect at the final stage of the combustion cycle. Further, since only one or a few kinds of powder mixture of the burnable poisons and the fissile materials is necessary, production and product control can be facilitated. (I.N.)

  9. A Hierarchical Z-Scheme α-Fe2 O3 /g-C3 N4 Hybrid for Enhanced Photocatalytic CO2 Reduction.

    Science.gov (United States)

    Jiang, Zhifeng; Wan, Weiming; Li, Huaming; Yuan, Shouqi; Zhao, Huijun; Wong, Po Keung

    2018-03-01

    The challenge in the artificial photosynthesis of fossil resources from CO 2 by utilizing solar energy is to achieve stable photocatalysts with effective CO 2 adsorption capacity and high charge-separation efficiency. A hierarchical direct Z-scheme system consisting of urchin-like hematite and carbon nitride provides an enhanced photocatalytic activity of reduction of CO 2 to CO, yielding a CO evolution rate of 27.2 µmol g -1 h -1 without cocatalyst and sacrifice reagent, which is >2.2 times higher than that produced by g-C 3 N 4 alone (10.3 µmol g -1 h -1 ). The enhanced photocatalytic activity of the Z-scheme hybrid material can be ascribed to its unique characteristics to accelerate the reduction process, including: (i) 3D hierarchical structure of urchin-like hematite and preferable basic sites which promotes the CO 2 adsorption, and (ii) the unique Z-scheme feature efficiently promotes the separation of the electron-hole pairs and enhances the reducibility of electrons in the conduction band of the g-C 3 N 4 . The origin of such an obvious advantage of the hierarchical Z-scheme is not only explained based on the experimental data but also investigated by modeling CO 2 adsorption and CO adsorption on the three different atomic-scale surfaces via density functional theory calculation. The study creates new opportunities for hierarchical hematite and other metal-oxide-based Z-scheme system for solar fuel generation. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Fuel storage

    International Nuclear Information System (INIS)

    Palacios, C.; Alvarez-Miranda, A.

    2009-01-01

    ENSA is a well known manufacturer of multi-system primary components for the nuclear industry and is totally prepared to satisfy future market requirements in this industry. At the same time that ENSA has been gaining a reputation world wider for the supply of primary components, has been strengthening its commitment and experience in supplying spent fuel components, either pool racks or storage and transportation casks, and offers not only fabrication but also design capabilities for its products. ENSA has supplied Spent Fuel Pool Racks, in spain, Finland, Taiwan, Korea, China, and currently it is in the process of licensing its own rack design in the United States of America for the ESBWR along with Ge-Hitachi. ENSA has supplied racks for 20 pools and 22 different reactors and it has also manufactured racks under all available technologies and developed a design known as Interlock Cell Matrix whose main features are outlined in this article. Another ENSA achievement in rack technology is the use of remote control for re-racking activities instead of using divers, which improves the ALARA requirements. Regarding casks for storage and transportation, ENSA also has al leading worldwide position, with exports prevailing over the Spanish market where ENSA has supplied 16 storage and transportation casks to the Spanish nuclear power Trillo. In some cases, ENSA acts as subcontractor for other clients. Foreign markets are still a major challenge for ENSA. ENSA-is well known for its manufacturing capabilities in the nuclear industry, but has been always involved in design activities through its engineering division, which carries out different tasks: components Design; Tooling Design; Engineering and Documentation; Project Engineering; Calculations, Design and Development Engineering. (Author)

  11. Photocatalytic oxidation dynamics of acetone on TiO2: tight-binding quantum chemical molecular dynamics study

    International Nuclear Information System (INIS)

    Lv Chen; Wang Xiaojing; Agalya, Govindasamy; Koyama, Michihisa; Kubo, Momoji; Miyamoto, Akira

    2005-01-01

    The clarification of the excited states dynamics on TiO 2 surface is important subject for the design of the highly active photocatalysts. In the present study, we applied our novel tight-binding quantum chemical molecular dynamics method to the investigation on the photocatalytic oxidation dynamics of acetone by photogenerated OH radicals on the hydrated anatase TiO 2 surface. The elucidated photocatalytic reaction mechanism strongly supports the previous experimental proposal and finally the effectiveness of our new approach for the clarification of the photocatalytic reaction dynamics employing the large simulation model was confirmed

  12. Nuclear fuel replacement device

    International Nuclear Information System (INIS)

    Ritz, W.C.; Robey, R.M.; Wett, J.F.

    1984-01-01

    A fuel handling arrangement for a liquid metal cooled nuclear reactor having a single rotating plug eccentric to the fuel core and a fuel handling machine radially movable along a slot in the plug with a transfer station disposed outside the fuel core but covered by the eccentric plug and within range of movement of said fuel handling machine to permit transfer of fuel assemblies between the core and the transfer station. (author)

  13. CANDU fuel performance

    International Nuclear Information System (INIS)

    Ivanoff, N.V.; Bazeley, E.G.; Hastings, I.J.

    1982-01-01

    CANDU fuel has operated successfully in Ontario Hydro's power reactors since 1962. In the 19 years of experience, about 99.9% of all fuel bundles have performed as designed. Most defects occurred before 1979 and subsequent changes in fuel design, fuel management, reactor control, and manufacturing quality control have reduced the current defect rate to near zero. Loss of power production due to defective fuel has been negligible. The outstanding performance continues while maintaining a low unit energy cost for fuel

  14. Fuels Combustion Research: Supercritical Fuel Pyrolysis

    National Research Council Canada - National Science Library

    Glassman, Irvin

    2001-01-01

    .... The focus during the subject period was directed to understanding the pyrolysis and combustion of endothermic fuels under subcritical conditions and the pyrolysis of these fuels under supercritical conditions...

  15. Fuels Combustion Research: Supercritical Fuel Pyrolysis

    National Research Council Canada - National Science Library

    Glassman, Irvin

    2000-01-01

    .... The focus during the subject period was directed to understanding the pyrolysis and combustion of endothermic fuels under subcritical conditions and the pyrolysis of these fuels under supercritical conditions...

  16. GSPEL - Fuel Cell Laboratory

    Data.gov (United States)

    Federal Laboratory Consortium — The Fuel Cell Lab (FCL)Established to investigate, integrate, testand verifyperformance and technology readiness offuel cell systems and fuel reformers for use with...

  17. Fuel performance experience

    International Nuclear Information System (INIS)

    Sofer, G.A.

    1986-01-01

    The history of LWR fuel supply has been characterized by a wide range of design developments and fuel cycle cost improvements. Exxon Nuclear Company, Inc. has pursued an aggressive fuel research and development program aimed at improved fuel performance. Exxon Nuclear has introduced many design innovations which have improved fuel cycle economics and operating flexibility while fuel failures remain at very low levels. The removable upper tie plate feature of Exxon Nuclear assemblies has helped accelerate this development, enabling repeated inspections during successive plant outages. Also, this design feature has made it possible to repair damaged fuel assemblies during refueling outages, thereby minimizing the economic impact of fuel failure from all causes

  18. Catalytic Fuel Conversion Facility

    Data.gov (United States)

    Federal Laboratory Consortium — This facility enables unique catalysis research related to power and energy applications using military jet fuels and alternative fuels. It is equipped with research...

  19. HTGR fuel reprocessing technology

    International Nuclear Information System (INIS)

    Brooks, L.H.; Heath, C.A.; Shefcik, J.J.

    1976-01-01

    The following aspects of HTGR reprocessing technology are discussed: characteristics of HTGR fuels, criteria for a fuel reprocessing flowsheet; selection of a reference reprocessing flowsheet, and waste treatment

  20. Degradation of ethylenethiourea pesticide metabolite from water by photocatalytic processes.

    Science.gov (United States)

    Bottrel, Sue Ellen C; Amorim, Camila C; Leão, Mônica M D; Costa, Elizângela P; Lacerda, Igor A

    2014-01-01

    In this study, photocatalytic (photo-Fenton and H2O2/UV) and dark Fenton processes were used to remove ethylenethiourea (ETU) from water. The experiments were conducted in a photo-reactor with an 80 W mercury vapor lamp. The mineralization of ETU was determined by total organic carbon analysis, and ETU degradation was qualitatively monitored by the reduction of UV absorbance at 232 nm. A higher mineralization efficiency was obtained by using the photo-peroxidation process (UV/H2O2). Approximately 77% of ETU was mineralized within 120 min of the reaction using [H2O2]0 = 400 mg L(-1). The photo-Fenton process mineralized 70% of the ETU with [H2O2]0 = 800 mg L(-1) and [Fe(2+)] = 400 mg L(-1), and there is evidence that hydrogen peroxide was the limiting reagent in the reaction because it was rapidly consumed. Moreover, increasing the concentration of H2O2 from 800 mg L(-1) to 1200 mg L(-1) did not enhance the degradation of ETU. Kinetics studies revealed that the pseudo-second-order model best fit the experimental conditions. The k values for the UV/H2O2 and photo-Fenton processes were determined to be 6.2 × 10(-4) mg L(-1) min(-1) and 7.7 × 10(-4) mg L(-1) min(-1), respectively. The mineralization of ETU in the absence of hydrogen peroxide has led to the conclusion that ETU transformation products are susceptible to photolysis by UV light. These are promising results for further research. The processes that were investigated can be used to remove pesticide metabolites from drinking water sources and wastewater in developing countries.

  1. Site remediation using photocatalytic VOC destruction of chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Brunet, R.A.H.; Pearcey, R.; Kittrell, J.R.; Mackin, G.; Wise, C.A.

    1999-07-01

    An innovative environmental technology has been developed and demonstrated for cost-effective control of toxic air emissions, such as trichloroethylene (TCE) and perchloroethylene (PCE), found in soil and groundwater at hazardous waste sites and in industrial effluents. The technology uses UV light and a proprietary photocatalyst to adsorb and destroy pollutants at ambient conditions, even with high humidity. Air stripping and soil vapor extraction efficiently transfer the pollutants to the gas phase, where they can be economically treated by photocatalysis without the risk of hazardous by-product formation. The AIR2000 photocatalytic technology was successfully installed at the Stamina Mills Superfund site in Rhode Island, where a commercial scale unit is treating 700 cfm of up to 1,000 ppm TCE, mixed with PCE, dichloroethylene (DCE), trichloroethane (TCA), and vinyl chloride (VC) produced through a combination of soil vapor extraction (SVE) and air stripping. As part of the EPA SITE program, the system was monitored for overall destruction removal efficiency (DRE) and hazardous by-product formation. A DRE in excess of 99% was reported over the first four months of operation, with greater than 99.99% DRE achieved, without production of hazardous by-products. The operating cost of the system is approximately 20% of activated carbon adsorption, which provides approximately $1,500,000 in cost savings over the life of the Stamina Mills project. The Adsorption Integrated Reaction (AIR) process is the recipient of the 1997 SBIR Technology of the Year award, the 1998 EPA Environmental Technology Innovator Award, and the 1998 R and D 100 Award.

  2. Basic dye decomposition kinetics in a photocatalytic slurry reactor

    International Nuclear Information System (INIS)

    Wu, C.-H.; Chang, H.-W.; Chern, J.-M.

    2006-01-01

    Wastewater effluent from textile plants using various dyes is one of the major water pollutants to the environment. Traditional chemical, physical and biological processes for treating textile dye wastewaters have disadvantages such as high cost, energy waste and generating secondary pollution during the treatment process. The photocatalytic process using TiO 2 semiconductor particles under UV light illumination has been shown to be potentially advantageous and applicable in the treatment of wastewater pollutants. In this study, the dye decomposition kinetics by nano-size TiO 2 suspension at natural solution pH was experimentally studied by varying the agitation speed (50-200 rpm), TiO 2 suspension concentration (0.25-1.71 g/L), initial dye concentration (10-50 ppm), temperature (10-50 deg. C), and UV power intensity (0-96 W). The experimental results show the agitation speed, varying from 50 to 200 rpm, has a slight influence on the dye decomposition rate and the pH history; the dye decomposition rate increases with the TiO 2 suspension concentration up to 0.98 g/L, then decrease with increasing TiO 2 suspension concentration; the initial dye decomposition rate increases with the initial dye concentration up to a certain value depending upon the temperature, then decreases with increasing initial dye concentration; the dye decomposition rate increases with the UV power intensity up to 64 W to reach a plateau. Kinetic models have been developed to fit the experimental kinetic data well

  3. The synthesis and photocatalytic activity of ZnSe microspheres

    International Nuclear Information System (INIS)

    Cao Huaqiang; Xiao Yujiang; Zhang Sichun

    2011-01-01

    This paper reports the synthesis of semiconductor ZnSe microspheres composed of nanoparticles via a solvothermal route between the organic molecule selenophene (C 4 H 4 Se) and ZnCl 2 without adding any surfactant. The ZnSe microspheres were characterized by x-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), specific surface area measurement, and photoluminescence (PL) spectra. A strong and broad blue PL emission at 443 nm in wavelength (∼2.79 eV in photon energy) is attributed to the near-band-edge (NBE) emission of ZnSe, while the 530 nm peak is a defect-related (DL) emission. The photocatalytic activity of the as-prepared ZnSe microspheres was evaluated by photodegradation of methyl orange (MO) dye under ultraviolet (UV) light and visible light irradiation. The degradations of MO reach 94% or 95.1%, close to 100%, in the presence of the as-synthesized ZnSe microspheres or commercial ZnSe powder after 7 or 10 h under UV irradiation, respectively. Meanwhile the degradations of MO reach 94.3% or 60.6% in the presence of the as-synthesized ZnSe microspheres or commercial ZnSe powder after 12 h, respectively. The degradation rate of ZnSe microspheres is twice that of ZnSe commercial powder under UV light irradiation, and three times under visible light irradiation. The degradation process of MO dye on ZnSe microspheres under UV or visible light is also discussed.

  4. Photocatalytic water splitting with acridine dyes: Guidelines from computational chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xiaojun [Department of Chemistry, Technical University of Munich, D-85747 Garching (Germany); Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University, Beijing 100044 (China); Karsili, Tolga N.V. [Department of Chemistry, Technical University of Munich, D-85747 Garching (Germany); Sobolewski, Andrzej L. [Institute of Physics, Polish Academy of Sciences, PL-02668 Warsaw (Poland); Domcke, Wolfgang, E-mail: domcke@ch.tum.de [Department of Chemistry, Technical University of Munich, D-85747 Garching (Germany)

    2016-01-13

    Highlights: • Photoexcited acridine dyes are able to abstract a hydrogen atom from water. • Photodetachment of the hydrogen atom from the radicals regenerates the catalyzer. • The reaction mechanisms were characterized with ab initio electronic-structure calculations. • The chromophores and radicals absorb within the range of the solar spectrum. - Abstract: The photocatalytic splitting of water into H{sup ·} and OH{sup ·} radicals in hydrogen-bonded chromophore-water complexes has been explored with computational methods for the chromophores acridine orange (AO) and benzacridine (BA). These dyes are strong absorbers within the range of the solar spectrum. It is shown that low-lying charge-transfer excited states exist in the hydrogen-bonded AO−H{sub 2}O and BA−H{sub 2}O complexes which drive the transfer of a proton from water to the chromophore, which results in AOH{sup ·}−OH{sup ·} or BAH{sup ·}−OH{sup ·} biradicals. The AOH{sup ·} and BAH{sup ·} radicals possess bright ππ{sup ∗} excited states with vertical excitation energies near 3.0 eV which are predissociated by a low-lying repulsive πσ{sup ∗} state. The conical intersections of the πσ{sup ∗} state with the ππ{sup ∗} excited states and the ground state provide a mechanism for the photodetachment of the H-atom by a second photon. Our results indicate that AO and BA are promising chromophores for water splitting with visible light.

  5. Indoor air purification using heterogeneous photocatalytic oxidation. Part I: Experimental study

    NARCIS (Netherlands)

    Yu, Q.; Brouwers, H.J.H.

    2009-01-01

    Heterogeneous photocatalytic oxidation (PCO) has shown to be a promising air purifying technology in outdoor conditions using TiO2 as photocatalyst activated with UV light. Also to indoor air quality more and more attention is paid because of the very important role it plays on human health, and it

  6. Temperature dependent optical characterization of Ni-TiO2 thin films as potential photocatalytic material

    Science.gov (United States)

    De, Rajnarayan; Haque, S. Maidul; Tripathi, S.; Rao, K. Divakar; Singh, Ranveer; Som, T.; Sahoo, N. K.

    2017-09-01

    Along with other transition metal doped titanium dioxide materials, Ni-TiO2 is considered to be one of the most efficient materials for catalytic applications due to its suitable energy band positions in the electronic structure. The present manuscript explores the possibility of improving the photocatalytic activity of RF magnetron sputtered Ni-TiO2 films upon heat treatment. Optical, structural and morphological and photocatalytic properties of the films have been investigated in detail for as deposited and heat treated samples. Evolution of refractive index (RI) and total film thickness as estimated from spectroscopic ellipsometry characterization are found to be in agreement with the trend in density and total film thickness estimated from grazing incidence X-ray reflectivity measurement. Interestingly, the evolution of these macroscopic properties were found to be correlated with the corresponding microstructural modifications realized in terms of anatase to rutile phase transformation and appearance of a secondary phase namely NiTiO3 at high temperature. Corresponding morphological properties of the films were also found to be temperature dependent which leads to modifications in the grain structure. An appreciable reduction of optical band gap from 2.9 to 2.5 eV of Ni-TiO2 thin films was also observed as a result of post deposition heat treatment. Testing of photocatalytic activity of the films performed under UV illumination demonstrates heat treatment under atmospheric ambience to be an effective means to enhance the photocatalytic efficiency of transition metal doped titania samples.

  7. Synthesis and Photocatalytic Performance of RGO/ZnO Nanorod Composites

    Directory of Open Access Journals (Sweden)

    LU Jia

    2016-12-01

    Full Text Available ZnO nanorods and RGO/ZnO nanorods composites were prepared by hydrothermal method. The influence of RGO content on the photocatalytic activity of RGO/ZnO nanorods composites was studied. ZnO nanorods and RGO/ZnO nanocomposites were characterized by X-ray diffraction (XRD, field emission electron microscopy (FESEM, X-ray photoelectron spectroscopy (XPS and diffuse reflectance UV-visible absorption spectroscopy techniques. The results show that RGO/ZnO samples are synthesized successfully. With different additions of GO, the RGO/ZnO samples obtained exhibit different absorption characteristics in visible light region. The photocatalytic results of using methyl orange (MO as the simulated pollutant show that RGO/ZnO nanorods composites exhibit high degradation efficiency under UV-Vis light illumination. The highest photocatalytic performance is obtained for RGO/ZnO composites when the mass ratio of RGO to ZnO is 3%. MO is almost completely degraded in 120min. RGO/ZnO also shows the visible-light-driven photocatalytic activity under visible light illumination (λ>400nm, and the maximum MO degradation efficiency in 180min can reach 26.2%, meanwhile, RGO/ZnO samples exhibit good photostability.

  8. Carrier-selective p- and n-contacts for efficient and stable photocatalytic water reduction

    DEFF Research Database (Denmark)

    Bae, Dowon; Pedersen, Thomas; Seger, Brian

    2017-01-01

    The successful realization of carrier-selective contacts for crystalline silicon (c-Si) based device for pho-tocatalytic hydrogen production has been demonstrated. The proposed TiO2protected carrier-selectivecontacts resemble a metal-oxide-semiconductor configuration, including a highly-doped nan...

  9. Synthesis, Analysis, and Testing of BiOBr-Bi2WO6 Photocatalytic Heterojunction Semiconductors

    Directory of Open Access Journals (Sweden)

    Xiangchao Meng

    2015-01-01

    Full Text Available In photocatalysis, the recombination of electron-hole pairs is generally regarded as one of its most serious drawbacks. The synthesis of various composites with heterojunction structures has increasingly shed light on preventing this recombination. In this work, a BiOBr-Bi2WO6 photocatalytic heterojunction semiconductor was synthesized by the facile hydrothermal method and applied in the photocatalytic degradation process. It was determined that both reaction time and temperature significantly affected the crystal structure and morphologies of the photocatalysts. BiOBr (50 at%-Bi2WO6 composites were prepared under optimum synthesis conditions (120°C for 6 h and by theoretically analyzing the DRS results, it was determined that they possessed the suitable band gap (2.61 eV to be stimulated by visible-light irradiation. The photocatalytic activities of the as-prepared photocatalysts were evaluated by the degradation of Rhodamine B (RhB under visible-light irradiation. The experimental conditions, including initial concentration, pH, and catalyst dosage, were explored and the photocatalysts in this system were proven stable enough to be reused for several runs. Moreover, the interpreted mechanism of the heterojunction enhancement effect proved that the synthesis of a heterojunction structure provided an effective method to decrease the recombination rate of the electron-hole pairs, thereby improving the photocatalytic activity.

  10. A generic model for photocatalytic activity as a function of catalyst thickness

    DEFF Research Database (Denmark)

    Nielsen, Morten G.; In, Su-Il; Vesborg, Peter C.K.

    2012-01-01

    Photocatalytically active thin films of TiO2 on transparent supports display different activities depending on the direction of illumination in relation to the reactant gas. In the case, where illumination and reactant gas are both supplied from the same side, the activity goes toward an asymptot...

  11. Synthesis and photocatalytic properties of different SnO2 microspheres on graphene oxide sheets

    Science.gov (United States)

    Wei, Jia; Xue, Shaolin; Xie, Pei; Zou, Rujia

    2016-07-01

    Different SnO2 microspheres like dandelions, silkworm cocoons and urchins have been synthesized on graphene oxide sheets (GOs) by hydrothermal method at 190 °C for 24 h. The morphologies, structures, chemical compositions and optical properties of the as-grown SnO2 microspheres on GOs (SMGs) were characterized by X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), X-ray energy dispersive spectrometer (EDS), Raman spectra and UV-vis diffuse reflectance spectra (DRS) techniques. The results of XRD revealed that the as-grown SnO2 microspheres have tetragonal rutile structure. The results of Raman spectra, EDS, XRD, XPS and SEM showed that the SnO2 microspheres were grown on GOs and the average diameter of dandelion-like microsphere was about 1.5 μm. The formation mechanism of SnO2 microspheres grown on GOs was discussed. The photocatalytic activity of the SMGs composites was evaluated by photocatalytic degradation of Rhodamine B (Rh B) aqueous solution under visible light irradiation. The photocatalytic results showed that the dandelion-like SMGs exhibited a much better photocatalytic activity than those of smooth and rough SMGs.

  12. Facile synthesis of carbon-ZnO nanocomposite with enhanced visible light photocatalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Akir, Sana [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021, Bizerte (Tunisia); Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopôle de Bordj Cedria, BP73, 8027, Soliman (Tunisia); Hamdi, Abderrahmane [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021, Bizerte (Tunisia); Laboratory of Semi-conductors, Nano-structures and Advanced Technologies, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050, Hammam-Lif (Tunisia); Addad, Ahmed [UMET, UMR CNRS 8207, Université Lille 1, 59655 Villeneuve d' Ascq Cédex (France); Coffinier, Yannick [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Boukherroub, Rabah, E-mail: rabah.boukherroub@iemn.univ-lille1.fr [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); and others

    2017-04-01

    Highlights: • C-ZnO nanocomposite was successfully prepared via a facile and eco-friendly process. • C-ZnO NPs have excellent photocatalytic activity for RhB dye degradation under visible light irradiation compared with literature. • The visible photocatalytic properties originate from injection e{sup −} in CB of ZnO from RhB. - Abstract: The present study describes a facile route for synthesis of carbon-ZnO nanocomposites (C-ZnO) via hydrothermal process in presence of glucose as carbon precursor. The samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) measurements. The results showed carbon uniformly coated on the surface of the ZnO nanoparticles to form the C-ZnO nanocomposites. Further investigation revealed that carbon could significantly protect ZnO NPs against the coalescence during high temperature treatment. The obtained C-ZnO nanocomposite showed excellent photocatalytic activity for the degradation of rhodamine B (RhB) under visible light irradiation, which was attributed to the repressed charge carrier recombination in the nanocomposite. Quenching experiments and photocurrent measurements revealed a photocatalytic mechanism occurring through photosensitization.

  13. Influence of Ti–O–Si hetero-linkages in the photocatalytic degradation of Rhodamine B

    NARCIS (Netherlands)

    Rasalingam, S; Kibombo, H.S.; Wu, C.M.; Budhi, S.; Peng, R.; Baltrusaitis, Jonas; Koodali, R.T.

    2013-01-01

    The influence of Ti–O–Si hetero-linkages in the degradation of Rhodamine B (RhB) dye over TiO2–SiO2 xerogels is exemplified by XPS analysis. We demonstrate a relationship between the percentage surface content of Ti–O–Si and the rate of photocatalytic degradation of RhB. Our detailed surface

  14. Characterization and photocatalytic activity of boron-doped TiO2 thin ...

    Indian Academy of Sciences (India)

    Wintec

    Chen Daimai, Wang Dong Yang and Jiang Zhongyi 2006 Ind. Eng. Chem. 45 4110. Cheng Jen-hao 2003 A study on photocatalytic oxidation of aque- ous chlorobenzene solution by nanostructured film of TiO2,. Master Thesis, National Sun Yat-Sen University, Taiwan. Deki S, Henin Yu Yu Ko, Fujita T, Akamatsu K, Mizuhata ...

  15. Inactivation of E. Coli in Water Using Photocatalytic, Nanostructured Films Synthesized by Aerosol Routes

    Directory of Open Access Journals (Sweden)

    Pratim Biswas

    2013-03-01

    Full Text Available TiO2 nanostructured films were synthesized by an aerosol chemical vapor deposition (ACVD method with different controlled morphologies: columnar, granular, and branched structures for the photocatalytic inactivation of Escherichia coli (E. coli in water. Effects of film morphology and external applied voltage on inactivation rate were investigated. As-prepared films were characterized using scanning electron microscopy (SEM, transmission electron microscopy (TEM, X-ray diffractometry (XRD, and UV-VIS. Photocatalytic and photoelectrochemical inactivation of E. coli using as-prepared TiO2 films were performed under irradiation of UVA light (note: UVA has a low efficiency to inactivate E. coli. Inactivation rate constants for each case were obtained from their respective inactivation curve through a 2 h incubation period. Photocatalytic inactivation rate constants of E. coli are 0.02/min (using columnar films, and 0.08/min (using branched films. The inactivation rate constant for the columnar film was enhanced by 330% by applied voltage on the film while that for the branched film was increased only by 30%. Photocatalytic microbial inactivation rate of the columnar and the branched films were also compared taking into account their different surface areas. Since the majority of the UV radiation that reaches the Earth’s surface is UVA, this study provides an opportunity to use sunlight to efficiently decontaminate drinking water.

  16. Synthesis, characterization and photocatalytic activity of LaMnO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Shaterian, Maryam, E-mail: shaterian@znu.ac.ir [Department of Chemistry, Faculty of Science, University of Zanjan, Zanjan 45371-38791, Islamic Republic of Iran (Iran, Islamic Republic of); Enhessari, Morteza [Department of Chemistry, Islamic Azad University, Naragh Branch, Naragh, Islamic Republic of Iran (Iran, Islamic Republic of); Rabbani, Davarkhah [Department of Environmental Health Engineering, School of Health, Kashan University of Medical Sciences, Kashan, Islamic Republic of Iran (Iran, Islamic Republic of); Asghari, Morteza [Separation Processes Research Group (SPRG), Department of Engineering, University of Kashan, Kashan, PO Box 87317-51167, Islamic Republic of Iran (Iran, Islamic Republic of); Salavati-Niasari, Masoud [Institute of Nano Science and Nano Technology, University of Kashan, Kashan, PO Box 87317-51167, Islamic Republic of Iran (Iran, Islamic Republic of)

    2014-11-01

    Highlights: • Visible-light sensitive LaMnO3 nanoparticles were synthesized via sol–gel process. • Structural and optical properties of photocatalysts have been investigated. • The photocatalytic activity was evaluated by the degradation of methyl orange as a model of pollutant. • The prepared nanocrystals showed good visible-light photocatalytic activity for the degradation of methyl orange. - Abstract: Visible-light sensitive LaMnO{sub 3} nanoparticles were synthesized via sol–gel process using stearic acid as complexing reagent. Characterizations of the resulting powders were carried out by means of X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and diffuse reflectance spectroscopy (DRS). Further, the photocatalytic activity of LaMnO{sub 3} was evaluated by degradation of methyl orange in aqueous solution under visible-light irradiation. The prepared nanoparticles showed excellent visible-light photocatalytic ability for the degradation of methyl orange so that, 60 ppm of nanoparticles can decolorizes the methyl orange solution (6 ppm) up to 98% in 90 min.

  17. Photocatalytic disinfection of spoilage bacteria Pseudomonas fluorescens and Macrococcus caseolyticus by nano-TiO2

    Science.gov (United States)

    Photocatalytic disinfection of spoilage bacteria gram-negative (G-) P. fluorescens and gram-positive (G+) M. caseolyticus by nano-TiO2 under different experimental conditions and the disinfection mechanism were investigated. The experimental conditions included the initial bacterial populations, nan...

  18. TIO2 based photocatalytic gas purification: the effects of co-catalysts and process conditions

    NARCIS (Netherlands)

    Fraters, B.D.

    2015-01-01

    Photocatalysis is highly promising as a technology to mitigate environmental pollution. In this thesis the focus will be on air purification by photocatalytic oxidation of volatile organic compounds (VOC’s). A major challenge in photocatalysis is the low photonic efficiency, due to high electron

  19. Photocatalytic methane decomposition over vertically aligned transparent TiO2 nanotube arrays

    DEFF Research Database (Denmark)

    In, Su-il; Nielsen, Morten Godtfred; Vesborg, Peter Christian Kjærgaard

    2011-01-01

    Vertically aligned transparent TiO2 nanotube arrays grown by the one-step anodic oxidation technique (on non-conductive supports such as Pyrex) and their photocatalytic performance for methane decomposition in a single-pass micro-fabricated reactor under UV light....

  20. Synthesis and Photocatalytic Activity of Zn Cd S/TiO ...

    African Journals Online (AJOL)

    NICOLAAS

    Synthesis and Photocatalytic Activity of Zn x. Cd. 1–x ... Electrospinning and Hydrothermal Method. Wei Changa,b,* ... conductor composites such as CdS,9 SnO,10 PbS11. .... 280 nm. ZnxCd1–xS nanoparticles grew on the surface of TiO2 with.

  1. Ag modified LaCoO3 perovskite oxide for photocatalytic application

    Science.gov (United States)

    Jayapandi, S.; Prakasini, V. Anitha; Anitha, K.

    2018-04-01

    The present investigation has been carried out to develop a novel photocatalytic material based on lanthanum cobaltite (LaCoO3) and silver (Ag) doped LaCoO3 perovskite oxide. Pure LaCoO3 and 5 Mol% Ag doped LaCoO3 (Ag-LaCoO3) have been synthesized by simple co-precipitation method and characterized by X-ray diffraction (XRD), ultraviolet-visible (UV-Vis) and photoluminescence (PL) techniques and its photocatalytic activity was evaluated by photodegradation of methylene blue under sunlight irradiation. The observed XRD, UV and PL results indicate that Ag influences on the crystallite size and absorption coefficient of LaCoO3 perovskite oxide. The percentage of dye degradations was calculated as 60% and 99 % for LaCoO3 and 5 Mol% Ag-LaCoO3 pervoskite oxides respectively for 10 minutes (10 min) exposure to sunlight, which indicates that 5 mol% of Ag-LaCoO3, has better photodegradation activity. Hence, the present investigation confirms that Ag influences the photocatalytic activity of a material and the observations will be helpful for further developing new photocatalytic materials.

  2. Photocatalytic degradation of paraoxon-ethyl in aqueous solution using titania nanoparticulate film

    International Nuclear Information System (INIS)

    Prasad, G.K.; Ramacharyulu, P.V.R.K.; Kumar, J. Praveen; Srivastava, A.R.; Singh, Beer

    2012-01-01

    Photocatalytic degradation of paraoxon-ethyl (o,o-diethyl o-(4-nitrophenyl) phosphate), a well known surrogate of chemical warfare agents, in aqueous solution was studied by using titania nanoparticulate film. Reaction followed pseudo first order behaviour. Photolytic degradation reaction of paraoxon-ethyl demonstrated relatively low rate with a value of rate constant of 2.5 × 10 −3 min −1 . Whereas, degradation reaction in the presence of titania nanoparticulate film and UV light displayed enhanced rate with a value of rate constant of 6.9 × 10 −3 min −1 due to photocatalysis. Gas chromatography–mass spectrometry analysis showed the formation of p-nitrophenol, o,o-diethyl phosphonic acid, o-ethyl, diphosphonic acid, phosphoric acid, dimerized product of o,o-diethyl phosphonic acid, acetaldehyde, and carbon dioxide due to photocatalytic degradation of paraoxon-ethyl. It indicates that, photocatalytic degradation reaction begins with destruction of P–O–C bonds. Subsequently, P, C atoms were found to be oxidized gradually, and contributed to its photocatalytic degradation. - Highlights: ► Synthesis of titania nanoparticles by sol–gel method. ► Fabrication of titania nanoparticulate film by dip coating. ► Paraoxon ethyl degradation reactions followed pseudo first order behaviour. ► Paraoxon-ethyl degraded to non toxic compounds like CO 2 , acetaldehyde, and nitrophenol.

  3. Using Photocatalytic Oxidation and Analytic Techniques to Remediate Lab Wastewater Containing Methanol

    Science.gov (United States)

    Xiong, Qing; Luo, Mingliang; Bao, Xiaoming; Deng, Yurong; Qin, Song; Pu, Xuemei

    2018-01-01

    This experiment is dedicated to second-year and above undergraduates who are in their experimental session of the analytical chemistry course. Grouped students are required to use a TiO[subscript 2] photocatalytic oxidation process to treat the methanol-containing wastewater that resulted from their previous HPLC experiments. Students learn to…

  4. Photocatalytic activity of Fe-doped CaTiO₃ under UV-visible light.

    Science.gov (United States)

    Yang, He; Han, Chong; Xue, Xiangxin

    2014-07-01

    The photocatalytic degradation of methylene blue (MB) over Fe-doped CaTiO₃ under UV-visible light was investigated. The as-prepared samples were characterized using X-ray diffraction (XRD), scanning electron microscope (SEM) equipped with an energy dispersive spectrometer (EDS) system, Fourier transform infrared spectra (FT-IR), and UV-visible diffuse reflectance spectroscopy (DRS). The results show that the doping with Fe significantly promoted the light absorption ability of CaTiO₃ in the visible light region. The Fe-doped CaTiO₃ exhibited higher photocatalytic activity than CaTiO₃ for the degradation of MB. However, the photocatalytic activity of the Fe-doped CaTiO₃ was greatly influenced by the calcination temperature during the preparation process. The Fe-doped CaTiO₃ prepared at 500°C exhibited the best photocatalytic activity, with degradation of almost 100% MB (10ppm) under UV-visible light for 180 min. Copyright © 2014. Published by Elsevier B.V.

  5. Facile synthesis of Cu/tetrapod-like ZnO whisker compounds with enhanced photocatalytic properties

    Science.gov (United States)

    Liu, Hong; Liu, Huarong; Fan, Ximei

    2017-09-01

    Cu/tetrapod-like ZnO whisker (T-ZnOw) compounds were successfully synthesized using N2H4 \\cdot H2O as a reducing agent by a simple reduction method without any insert gas at room temperature. The crystal phase composition and morphology of the as-prepared samples were investigated by XRD, SEM and FESEM tests. The photocatalytic property of the as-prepared samples was detected by the degradation of methyl orange (MO) aqueous solution under UV irradiation. It can be found that Cu nanoparticles (CuNPs) dispersed on the surface of T-ZnOw increased with the increasing of Cu/Zn molar ratios (Cu/Zn MRs), and an octahedral structure of CuNPs was obtained when the sample was prepared with less than and equal to 7.30% Cu/Zn MR, but tended to a spherical or nanorod structure of CuNPs densely arranged on the surface of T-ZnOw, which is prepared by Cu/Zn MRs up to 22.00%. All the compounds exhibited excellent photocatalytic activity in decomposing of MO than T-ZnOw, the photocatalytic property of the samples increased with the increasing of Cu/Zn MRs up to 7.30%, while it decreases when further increasing the Cu/Zn MRs. The Schottky barrier of the Cu/T-ZnOw compound can effectively capture photoinduced electrons from the interface and enhanced the photocatalytic property of T-ZnOw.

  6. Structural, optical, magnetic and photocatalytic properties of Co doped CuS diluted magnetic semiconductor nanoparticles

    International Nuclear Information System (INIS)

    Sreelekha, N.; Subramanyam, K.; Amaranatha Reddy, D.; Murali, G.; Ramu, S.; Rahul Varma, K.; Vijayalakshmi, R.P.

    2016-01-01

    Highlights: • Cu_1_−_xCo_xS nanoparticles were synthesized via chemical co-precipitation method. • Structural, band gap, magnetization and photocatalysis studies were carried out. • All the doped samples exhibited intrinsic room temperature ferromagnetism. • Effect of magnetic properties on photocatalytic activity was analyzed. • CuS:Co nanoparticles may find applications in photocatalytic and spintronic devices. - Abstract: Pristine and Co doped covellite CuS nanoparticles were synthesized in aqueous solution by facile chemical co-precipitation method with Ethylene Diamine Tetra Acetic Acid (EDTA) as a stabilizing agent. EDAX measurements confirmed the presence of Co in the CuS host lattice. Hexagonal crystal structure of pure and Co doped CuS nanoparticles were authenticated by XRD patterns. TEM images indicated that sphere-shape of nanoparticles through a size ranging from 5 to 8 nm. The optical absorption edge moved to higher energies with increase in Co concentration as indicated by UV–vis spectroscopy. Magnetic measurements revealed that bare CuS sample show sign of diamagnetic character where as in Co doped nanoparticles augmentation of room temperature ferromagnetism was observed with increasing doping precursor concentrations. Photocatalytic performance of the pure and Co doped CuS nanoparticles were assessed by evaluating the degradation rate of rhodamine B solution under sun light irradiation. The 5% Co doped CuS nanoparticles provide evidence for high-quality photocatalytic activity.

  7. Core–shell TiO2 microsphere with enhanced photocatalytic activity and improved lithium storage

    International Nuclear Information System (INIS)

    Guo, Hong; Tian, Dongxue; Liu, Lixiang; Wang, Yapeng; Guo, Yuan; Yang, Xiangjun

    2013-01-01

    Inorganic hollow core–shell spheres have attracted considerable interest due to their singular properties and wide range of potential applications. Herein a novel facile generic strategy of combining template assisted and solvothermal alcoholysis is employed to prepare core–void–shell anatase TiO 2 nanoparticle aggregates with an excellent photocatalytic activity, and enhanced lithium storage in large quantities. Amorphous carbon can be loaded on the TiO 2 nanoparticles uniformly under a suitably formulated ethanol/water system in the solvothermal alcoholysis process, and the subsequent calcination results of the formation of core–shell–shell anatase TiO 2 nanoparticle aggregates. The intrinsic core–void–shell nature as well as high porosity of the unique nanostructures contributes greatly to the superior photocatalytic activity and improved performance as anode materials for lithium ion batteries. - Graphical abstract: A novel strategy of combining template assisted and solvothermal alcoholysis is employed to prepare unique core–void–shell anatase TiO 2 nanoparticle aggregates with the superior photocatalytic activity and improved lithium storage. Highlights: ► TiO 2 mesospheres are synthesized by solvothermal alcoholysis. ► It is core–void–shell structure and the thickness of shell is estimated to 80 nm. ► It exhibits a remarkable photocatalytic activity and improved lithium storage

  8. Studying Impact of Different Precipitating Agents on Crystal Structure, Morphology and Photocatalytic Activity of Bismuth Oxide

    Directory of Open Access Journals (Sweden)

    Yayuk Astuti

    2017-10-01

    How to Cite: Astuti, Y., Arnelli, Pardoyo, Fauziyah, A., Nurhayati, S., Wulansari, A.D., Andianingrum, R., Widiyandari, H., Bhaduri, G.A. (2017. Studying Impact of Different Precipitating Agents on Crystal Structure, Morphology and Photocatalytic Activity of Bismuth Oxide. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (3: 478-484 (doi:10.9767/bcrec.12.3.1144.478-484

  9. Photocatalytic degradation of malachite green dye using Au/NaNbO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Baeissa, E.S., E-mail: elhambaeissa@gmail.com

    2016-07-05

    The morphology of sodium niobate, which was produced using a hydrothermal method, was studied by changing the hydrothermal temperature from 100 to 250 °C. Using 250 °C hydrothermal temperature resulted in sodium niobate with a nanocube structure. The sodium niobate nanocubes were doped with gold by impregnation with an aqueous solution of HAuCl{sub 4}. The band gap of sodium niobate is approximately 3.4 eV, and it was decreased to 2.45 eV by gold doping. The surface area of sodium niobate is higher than that of Au/NaNbO{sub 3} due to blockage of some pores of sodium niobate by gold doping. The photocatalytic performance of gold-doped sodium niobate was studied by degradation of malachite green dye using visible light irradiation. The results demonstrate that the photocatalytic performance of gold-doped sodium niobate is higher than that of sodium niobate and TiO{sub 2} Degussa under visible light irradiation. - Highlights: • Au/NaNbO{sub 3} were used for photocatalytic degradation of malachite green dye. • Photocatalytic degradation was dependent on wt % of Au; reaction time, and weight of catalyst. • Catalyst re-use revealed the present photocatalyst remain effective and active after five cycles.

  10. Enhanced photocatalytic activity of BiOCl by C70 modification and mechanism insight

    Science.gov (United States)

    Ma, Dongmei; Zhong, Junbo; Li, Jianzhang; Wang, Li; Peng, Rufang

    2018-06-01

    As an excellent photocatalyst which can compete with TiO2, BiOCl has triggered increasing attention. However, the practical application of BiOCl has been significantly limited by the fast recombination of the photoinduced electron-hole charge pairs. In this study, to further enhance the separation efficiency of photoinduced electron-hole charge pairs of BiOCl, a series of efficient BiOCl photocatalysts were prepared by C70 surface modification. The trapping experiments reveal that the main active species were determined to be superoxide radicals (O2rad -) and holes (h+) under simulated sunlight irradiation. The surface photovoltage spectroscopy (SPS) demonstrates that separation of the photoinduced electron-hole pairs has been significantly promoted, forming more radOH, proven by terephthalic acid photoluminescence probing technique. The photocatalytic evaluation results display that the C70/BiOCl photocatalysts exhibit much higher photocatalytic activity in decolorization of rhodamine B (RhB) than that of the bare BiOCl under the simulated sunlight irradiation. The excellent electron acceptability of C70 is conducive to the separation of the photogenerated carriers and results in efficient formation of O2rad -, proven by the results of SPS and electron spin-resonance (ESR), therefore the photocatalytic performance of C70/BiOCl has been greatly improved. Based on all these observations, an enhancement mechanism in photocatalytic performance of C70/BiOCl was proposed.

  11. Facile synthesis of phosphorus doped graphitic carbon nitride polymers with enhanced visible-light photocatalytic activity

    International Nuclear Information System (INIS)

    Zhang, Ligang; Chen, Xiufang; Guan, Jing; Jiang, Yijun; Hou, Tonggang; Mu, Xindong

    2013-01-01

    Graphical abstract: - Highlights: • P-doped g-C 3 N 4 has been prepared by a one-pot green synthetic approach. • The incorporation of P resulted in favorable textural and electronic properties. • Doping with P enhanced the visible-light photocatalytic activity of g-C 3 N 4 . • A postannealing treatment further enhanced the activity of P-doped g-C 3 N 4 . • Photogenerated holes were the main species responsible for the activity. - Abstract: Phosphorus-doped carbon nitride materials were prepared by a one-pot green synthetic approach using dicyandiamide monomer and a phosphorus containing ionic liquid as precursors. The as-prepared materials were subjected to several characterizations and investigated as metal-free photocatalysts for the degradation of organic pollutants (dyes like Rhodamine B, Methyl orange) in aqueous solution under visible light. Results revealed that phosphorus-doped carbon nitride have a higher photocatalytic activity for decomposing Rhodamine B and Methyl orange in aqueous solution than undoped g-C 3 N 4 , which was attributed to the favorable textural, optical and electronic properties caused by doping with phosphorus heteroatoms into carbon nitride host. A facile postannealing treatment further improved the activity of the photocatalytic system, due to the higher surface area and smaller structural size in the postcalcined catalysts. The phosphorus-doped carbon nitride showed high visible-light photocatalytic activity, making them promising materials for a wide range of potential applications in photochemistry

  12. Photocatalytic degradation of textile dyestuffs using TiO{sub 2} nanotubes prepared by sonoelectrochemical method

    Energy Technology Data Exchange (ETDEWEB)

    Tekin, Derya, E-mail: deryatekin@atauni.edu.tr

    2014-11-01

    Highlights: • TiO{sub 2} nanotubes prepared by electrochemical and sonoelectrochemical method. • More regular TiO{sub 2} nanotubes diameters prepared by sonoelectrochemical method. • Obtained nanotubes were used in the photocatalytic degradation of Orange G dye. • TiO{sub 2} nanotubes prepared by sonoelectrochemical method showed 10% faster degradation of Orange G dye compared with the one by electrochemical method. - Abstract: TiO{sub 2} nanotubes were prepared by anodization of Ti plates by conventional electrochemical technique as well as by an emerging sonoelectrochemical technique. Scanning electron miscroscope (SEM) analysis showed that ultrasound assisted anodization yielded more ordered and controllable TiO{sub 2} tube banks with higher tube diameter. The photocatalytical activities of TiO{sub 2} nanotubes were tested in the photocatalytical degradation of Orange G dye. The results showed that sonoelectrochemically prepared TiO{sub 2} tubes exhibited 10% higher photocatalytic performance than the electrochemical prepared ones, and more than 18% higher activity than the other TiO{sub 2} samples.

  13. Novel preparation and photocatalytic activity of one-dimensional TiO2 hollow structures

    International Nuclear Information System (INIS)

    Yu Huogen; Yu Jiaguo; Cheng Bei; Liu Shengwei

    2007-01-01

    Usually, templated methods include two important steps: the coating of nanocrystals on the surface of the templates and the removal of the templates. In this study, one-dimensional TiO 2 hollow structures, based on the template-directed deposition and then in situ template-sacrificial reaction (or dissolution), were prepared by a one-step template method using vanadium oxide nanobelts as the templates and TiF 4 as the precursor at 60 deg. C. The coating of TiO 2 nanoparticles on the surface of the templates was accompanied with the dissolution of vanadium oxide nanobelts by HF produced during the hydrolysis of TiF 4 in the reaction solution. It was found that the prepared one-dimensional TiO 2 hollow structures with a mesoporous wall were composed of TiO 2 nanoparticles with a diameter of 10-55 nm, resulting in a large specific surface area (77.2 m 2 g -1 ) and high pore volume (0.13 cm 3 g -1 ), and the wall thickness of the TiO 2 hollow structures could be easily controlled by adjusting the precursor concentration of TiF 4 . The photocatalytic activity experiment indicated that the prepared one-dimensional TiO 2 hollow structures, which could be readily separated from a slurry system after photocatalytic reaction, exhibited obvious photocatalytic activity for the photocatalytic degradation of methyl orange aqueous solution

  14. Enhanced photocatalytic activity of titania-silica mixed oxide prepared via basic hydrolyzation

    International Nuclear Information System (INIS)

    Xie Chao; Xu Zili; Yang Qiujing; Xue Baoyong; Du Yaoguo; Zhang Jiahua

    2004-01-01

    Two different synthesis routes were applied to prepare TiO 2 -XSiO 2 (X denotes mol% of silica in titania-silica mixed oxides) with different silica concentrations by using ammonia water as hydrolysis catalyst. Through comparing the photocatalytic performance of two sets of mixed oxides, we found that the photocatalytic activity of mixed oxides prepared via the route which can promote homogeneity, was significantly enhanced as compared with that of counterparts prepared via the another route, and the highest photocatalytic activity obtained by adding about 9.1 mol% silica into titania was much higher than that of pure TiO 2 . The mixed oxides were investigated by means of XRD, thermal analysis, UV-vis, FT-IR and XPS. The characterization results suggest that, in comparison with pure TiO 2 , the mixed oxides exhibit smaller crystallite size and higher thermal stability which can elevate the temperature of anatase to rutile phase transformation due to the addition of silica. Furthermore, Broensted acidity, which is associated with the formation of Ti-O-Si hetero linkages where tetrahedrally coordinated silica is chemically mixed with the octahedral titania matrix, may be a very important contribution to the enhanced photocatalytic activity of titania-silica mixed oxides as well

  15. Photocatalytic degradation of malachite green dye using Au/NaNbO_3 nanoparticles

    International Nuclear Information System (INIS)

    Baeissa, E.S.

    2016-01-01

    The morphology of sodium niobate, which was produced using a hydrothermal method, was studied by changing the hydrothermal temperature from 100 to 250 °C. Using 250 °C hydrothermal temperature resulted in sodium niobate with a nanocube structure. The sodium niobate nanocubes were doped with gold by impregnation with an aqueous solution of HAuCl_4. The band gap of sodium niobate is approximately 3.4 eV, and it was decreased to 2.45 eV by gold doping. The surface area of sodium niobate is higher than that of Au/NaNbO_3 due to blockage of some pores of sodium niobate by gold doping. The photocatalytic performance of gold-doped sodium niobate was studied by degradation of malachite green dye using visible light irradiation. The results demonstrate that the photocatalytic performance of gold-doped sodium niobate is higher than that of sodium niobate and TiO_2 Degussa under visible light irradiation. - Highlights: • Au/NaNbO_3 were used for photocatalytic degradation of malachite green dye. • Photocatalytic degradation was dependent on wt % of Au; reaction time, and weight of catalyst. • Catalyst re-use revealed the present photocatalyst remain effective and active after five cycles.

  16. Facile synthesis of Bi/BiOCl composite with selective photocatalytic properties

    International Nuclear Information System (INIS)

    Chen, Dongling; Zhang, Min; Lu, Qiuju; Chen, Junfang; Liu, Bitao; Wang, Zhaofeng

    2015-01-01

    This paper presents a novel and facile method to fabricate Bi/BiOCl composites with dominant (001) facets in situ via a microwave reduction route. Different characterization techniques, including X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), transmission scanning electron microscopy (TEM), UV–vis diffuse reflectance spectrometry (DRS), X-ray photoelectron spectroscopy (XPS), electron spin resonance spectroscopy (ESR), cathodoluminescence spectrum (CL), and lifetime, have been employed to investigate the structure, optical and electrical properties of the Bi/BiOCl composites. The experimental results show that the introduction of Bi particles can efficiently enhance the photocatalytic performance of BiOCl for the degradation of several dyes under ultraviolet (UV) light irradiation, especially for negative charged methyl orange (MO). Unlike the UV photocatalytic performance, such Bi/BiOCl composite shows higher degradation efficiency towards rhodamine B (RhB) than MO and methylene blue (MB) under visible light irradiation. This special photocatalytic performance can be ascribed to the synergistic effect between oxygen vacancies and Bi particles. This work provides new insights about the photodegradation mechanisms of MO, MB and RhB under UV and visible light irradiation, which would be helpful to guide the selection of an appropriate catalyst for other pollutants. - Highlights: • Bi/BiOCl composites were synthesized via a microwave reduction. • Tunable selectivity photocatalytic activity can be achieved. • Photodegradation mechanism under UV and visible light were proposed

  17. Preparation of TiO2-Fullerene Composites and Their Photocatalytic Activity under Visible Light

    Directory of Open Access Journals (Sweden)

    Ken-ichi Katsumata

    2012-01-01

    Full Text Available The development of visible light-sensitive photocatalytic materials is being investigated. In this study, the anatase and rutile-C60 composites were prepared by solution process. The characterization of the samples was conducted by using XRD, UV-vis, FT-IR, Raman, and TEM. The photocatalytic activity of the samples was evaluated by the decolorization of the methylene blue. From the results of the Raman, FT-IR, and XRD, the existence of the C60 was confirmed in the samples. The C60 was modified on the anatase or rutile particle as a cluster. The C60 didn't have the photocatalytic activity under UV and visible light. The anatase and rutile-C60 composites exhibited lower photocatalytic activity than the anatase and rutile under UV light. The anatase-C60 exhibited also lower activity than the anatase under visible light. On the other hand, the rutile-C60 exhibited higher activity than the rutile under visible light. It is considered that the photogenerated electrons can transfer from the C60 to the rutile under visible light irradiation.

  18. Synthesis, photoelectrochemical properties and solar light-induced photocatalytic activity of bismuth ferrite nanoparticles

    Science.gov (United States)

    Pattnaik, Sambhu Prasad; Behera, Arjun; Martha, Satyabadi; Acharya, Rashmi; Parida, Kulamani

    2018-01-01

    Bismuth ferrite (BFO) nanoparticles prepared by solid state reaction route were characterized by various characterization techniques such as XRD, FESEM, HRTEM, UV-Vis DRS, PL etc., and their photocatalytic activities were evaluated by decolorization of aqueous solution of Congo red (CR) under solar light. The photocatalytic activity of BFO was increased by increasing the preparation temperature from 350 to 500 °C and then decreased with rise in temperature. The results of electrochemical measurements such as linear sweep voltammetry (LSV), electrochemical impedence (EIS), and Mott-Schottky analysis of BFO nanoparticles corroborated the findings of their photocatalytic activity. The enhanced photocatalytic response of the sample prepared at 500 °C is attributed to its smallest band gap, minimum crystallite size (30 nm), efficient separation, and lowest possible recombination of photo-generated charge carriers. The effects of amount of nano-BFO, irradiation time, initial CR concentration, and BFO calcination temperature on the decolorization of CR were examined. It was observed that 1 g/L nano-BFO calcined at 500 °C can decolorize up to 77% a 10-ppm CR dye solution under solar irradiation for 60 min. The studies included scavenger tests for identification of reactive species and a possible mechanism of dye decolorization.

  19. Efficient solar hydrogen production by photocatalytic water splitting: From fundamental study to pilot demonstration

    Energy Technology Data Exchange (ETDEWEB)

    Jing, Dengwei; Guo, Liejin; Zhao, Liang; Zhang, Ximin; Liu, Huan; Li, Mingtao; Shen, Shaohua; Liu, Guanjie; Hu, Xiaowei; Zhang, Xianghui; Zhang, Kai; Ma, Lijin; Guo, Penghui [State Key Lab of Multiphase Flow in Power Engineering, Xi' an Jiaotong University, 28 Xianning West Road, Xi' an 710049 (China)

    2010-07-15

    Photocatalytic water splitting with solar light is one of the most promising technologies for solar hydrogen production. From a systematic point of view, whether it is photocatalyst and reaction system development or the reactor-related design, the essentials could be summarized as: photon transfer limitations and mass transfer limitations (in the case of liquid phase reactions). Optimization of these two issues are therefore given special attention throughout our study. In this review, the state of the art for the research of photocatalytic hydrogen production, both outcomes and challenges in this field, were briefly reviewed. Research progress of our lab, from fundamental study of photocatalyst preparation to reactor configuration and pilot level demonstration, were introduced, showing the complete process of our effort for this technology to be economic viable in the near future. Our systematic and continuous study in this field lead to the development of a Compound Parabolic Concentrator (CPC) based photocatalytic hydrogen production solar rector for the first time. We have demonstrated the feasibility for efficient photocatalytic hydrogen production under direct solar light. The exiting challenges and difficulties for this technology to proceed from successful laboratory photocatalysis set-up up to an industrially relevant scale are also proposed. These issues have been the object of our research and would also be the direction of our study in future. (author)

  20. The impact of alkali metal halide electron donor complexes in the photocatalytic degradation of pentachlorophenol

    Energy Technology Data Exchange (ETDEWEB)

    Khuzwayo, Z., E-mail: zack.khuzwayo@up.ac.za; Chirwa, E.M.N

    2017-01-05

    Highlights: • Facilitation of photocatalysis using simple metal-halides as VB hole scavengers. • Recombination prevention by coupled valence and conduction band approaches. • Determination of anions critical levels beyond which process retardation occurs. • Determination of the photocatalytic process rate of reaction kinetics. - Abstract: The performance of photocatalytic oxidation of chemical pollutants is subjected to the presence of anion complexes in natural waters. This study investigated the influence of alkali metal (Na{sup +} (sodium), K{sup +} (potassium)) halides (Cl{sup −} (chloride), Br{sup −} (bromide), F{sup −} (fluoride)) as inorganic ion sources in the photocatalytic degradation of pentachlorophenol (PCP) in batch systems. It was found that the exclusive presence of halides in the absence of an electron acceptor adequately facilitated the photocatalyst process below critical levels of anion populations, where beyond the critical point the process was significantly hindered. Below the determined critical point, the performance in some cases near matches that of the facilitation of the photocatalytic process by exclusive oxygen, acting as an electron scavenger. The coupling of halide ions and oxygenation presented significantly improved photo-oxidation of PCP, this was confirmed by the inclusion of formic acid as a comparative electron donor. The Langmuir-Hinshelwood kinetic expression was used to calculate the performance rate kinetics. The probable impact of the halide anions was discussed with regards to the process of electron hole pair recombination prevention.

  1. Interfacial Structure and Photocatalytic Activity of Magnetron Sputtered TiO2 on Conducting Metal Substrates

    DEFF Research Database (Denmark)

    Daviðsdóttir, Svava; Petit, Jean-Pierre; Mermoux, Michel

    2014-01-01

    The photocatalytic behavior of magnetron sputtered anatase TiO2 coatings on copper, nickel, and gold was investigated with the aim of understanding the effect of the metallic substrate and coating-substrate interface structure. Stoichiometry and nanoscale structure of the coating were investigated...

  2. Microwave synthesis and photocatalytic activities of ZnO bipods with different aspect ratios

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Fazhe; Zhao, Zengdian [Analysis and Testing Center, Shandong University of Technology, Zibo 255100 (China); Qiao, Xueliang, E-mail: xuelqiao@163.com [State Key Laboratory of Plastic Forming Simulation and Die and Mould Technology, Huazhong University of Science and Technology, Wuhan 430074, Hubei (China); Tan, Fatang; Wang, Wei [State Key Laboratory of Plastic Forming Simulation and Die and Mould Technology, Huazhong University of Science and Technology, Wuhan 430074, Hubei (China)

    2016-02-15

    Highlights: • We synthesized linked ZnO nanorods by a facile microwave method. • The effect of reaction parameters on ZnO was investigated. • ZnO bipods with different aspect ratios were prepared. • The photocatalytic performance of ZnO bipods was evaluated. - Abstract: Linked ZnO nanorods have been successfully prepared via a facile microwave method without any post-synthesis treatment. The X-ray diffraction (XRD) patterns indicated the precursor had completely transformed into the pure ZnO crystal. The images of field emitting scanning electron microscope (FESEM) and transmission electron microscope (TEM) showed that linked ZnO nanorods consisted predominantly of ZnO bipods. The formation process of the ZnO bipods was clearly discussed. ZnO bipods with different aspect ratios have been obtained by tuning the concentrations of reagents and microwave power. Moreover, the photocatalytic performance of ZnO bipods with different aspect ratios for degradation of methylene blue was systematically evaluated. The results of photocatalytic experiments showed that the photocatalytic activity increased with the aspect ratios of ZnO bipods increased. The reason is that ZnO bipods with larger aspect ratio have higher surface area, which can absorb more MB molecules to react with ·OH radicals.

  3. Kinetic Study of Photocatalytic Reduction of CO2 over TiO2.

    Czech Academy of Sciences Publication Activity Database

    Kočí, K.; Obalová, L.; Šolcová, Olga

    2010-01-01

    Roč. 31, č. 3 (2010), s. 395-407 ISSN 0208-6425 R&D Projects: GA ČR GA104/09/0694 Institutional research plan: CEZ:AV0Z40720504 Keywords : titania * photocatalytic reduction * methane Subject RIV: CC - Organic Chemistry OBOR OECD: Organic chemistry Impact factor: 0.252, year: 2010

  4. Understanding promotion of photocatalytic activity of TiO2 by Au nanoparticles

    NARCIS (Netherlands)

    Amrollahi Buky, Rezvaneh; Hamdy, Mohamed S.; Mul, Guido

    2014-01-01

    Au nanoparticles prepared by deposition–precipitation were evaluated in promoting photocatalytic activity of TiO2 (P25) in the oxidation of methylcyclohexane. At 375 nm and in particular at 425 nm, Au was found to significantly enhance the rate induced by P25. Illumination of Au-promoted P25 at 525

  5. Photocatalytic degradation of crystal violet by thiourea-doped TiO2 ...

    African Journals Online (AJOL)

    In this study, optimisation of the photocatalytic behaviour of crystal violet (CV) by thiourea (Tu)-codoped TiO2 thin film in fixed bed photoreactor was investigated by central composite designs (CCDs). The effective variables were pH, the concentration of CV dye, flow rate and reaction time. The results of the CCD model ...

  6. Synthesis, characterization and photocatalytic activity of LaMnO3 nanoparticles

    International Nuclear Information System (INIS)

    Shaterian, Maryam; Enhessari, Morteza; Rabbani, Davarkhah; Asghari, Morteza; Salavati-Niasari, Masoud

    2014-01-01

    Highlights: • Visible-light sensitive LaMnO3 nanoparticles were synthesized via sol–gel process. • Structural and optical properties of photocatalysts have been investigated. • The photocatalytic activity was evaluated by the degradation of methyl orange as a model of pollutant. • The prepared nanocrystals showed good visible-light photocatalytic activity for the degradation of methyl orange. - Abstract: Visible-light sensitive LaMnO 3 nanoparticles were synthesized via sol–gel process using stearic acid as complexing reagent. Characterizations of the resulting powders were carried out by means of X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and diffuse reflectance spectroscopy (DRS). Further, the photocatalytic activity of LaMnO 3 was evaluated by degradation of methyl orange in aqueous solution under visible-light irradiation. The prepared nanoparticles showed excellent visible-light photocatalytic ability for the degradation of methyl orange so that, 60 ppm of nanoparticles can decolorizes the methyl orange solution (6 ppm) up to 98% in 90 min

  7. Experimental research on photocatalytic oxidation air purification technology applied to aircraft cabins

    DEFF Research Database (Denmark)

    Sun, Yuexia; Fang, Lei; Wyon, David P.

    2005-01-01

    The experiment presented in this report was performed in a simulated aircraft cabin to evalu-ate the air cleaning effects of two air purification devices using Photocatalytic Oxidation (PCO) technology. Objective physical, chemical and physiological measurements and subjec-tive human assessments ...

  8. Structural, optical, magnetic and photocatalytic properties of Co doped CuS diluted magnetic semiconductor nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Sreelekha, N.; Subramanyam, K. [Department of Physics, Sri Venkateswara University, Tirupati 517502 (India); Department of Physics, Raghu Engineering College, Visakhapatnam, Andrapradesh 531162 (India); Amaranatha Reddy, D. [Department of Chemistry and Chemical Institute for Functional Materials, Pusan National University, Busan 609735 (Korea, Republic of); Murali, G. [Department of BIN Fusion Technology & Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, Jeonbuk (Korea, Republic of); Ramu, S. [Department of Physics, Sri Venkateswara University, Tirupati 517502 (India); Rahul Varma, K. [Department of Mechanical Engineering, University of California, Berkeley (United States); Vijayalakshmi, R.P., E-mail: vijayaraguru@gmail.com [Department of Physics, Sri Venkateswara University, Tirupati 517502 (India)

    2016-08-15

    Highlights: • Cu{sub 1−x}Co{sub x}S nanoparticles were synthesized via chemical co-precipitation method. • Structural, band gap, magnetization and photocatalysis studies were carried out. • All the doped samples exhibited intrinsic room temperature ferromagnetism. • Effect of magnetic properties on photocatalytic activity was analyzed. • CuS:Co nanoparticles may find applications in photocatalytic and spintronic devices. - Abstract: Pristine and Co doped covellite CuS nanoparticles were synthesized in aqueous solution by facile chemical co-precipitation method with Ethylene Diamine Tetra Acetic Acid (EDTA) as a stabilizing agent. EDAX measurements confirmed the presence of Co in the CuS host lattice. Hexagonal crystal structure of pure and Co doped CuS nanoparticles were authenticated by XRD patterns. TEM images indicated that sphere-shape of nanoparticles through a size ranging from 5 to 8 nm. The optical absorption edge moved to higher energies with increase in Co concentration as indicated by UV–vis spectroscopy. Magnetic measurements revealed that bare CuS sample show sign of diamagnetic character where as in Co doped nanoparticles augmentation of room temperature ferromagnetism was observed with increasing doping precursor concentrations. Photocatalytic performance of the pure and Co doped CuS nanoparticles were assessed by evaluating the degradation rate of rhodamine B solution under sun light irradiation. The 5% Co doped CuS nanoparticles provide evidence for high-quality photocatalytic activity.

  9. Indoor air purificaton using heterogeneous photocatalytic oxidation, Part 2: Kinetic study

    NARCIS (Netherlands)

    Yu, Q.; Ballari, M.; Brouwers, H.J.H.

    2010-01-01

    In part I to this article [1], the application of the heterogeneous photocatalytic oxidation (PCO) theory for the indoor air quality improvement was presented. With a modified TiO2 that can be activated by visible light as the photocatalyst coated on a special wall paper, and one typical indoor air

  10. Dependence of Photocatalytic Activity of TiO2-SiO2 Nanopowders

    Directory of Open Access Journals (Sweden)

    M. Riazian

    2014-10-01

    Full Text Available Structural properties and chemical composition change the photocatalytic activity in TiO2-SiO2 nanopowder composite. The SiO2-TiO2 nanostructure is synthesized based on sol–gel method. The nanoparticles are characterized by x-ray fluorescents (XRF, x- ray diffraction (XRD, tunneling electron microscopy (TEM, field emission scanning electron microscopy (FE-SEM, UV-vis. Spectrophotometer and furrier transmission create infrared absorption (FTIR techniques. The rate constant k for the degradation of methylen blue in its aqueous solution under UV irradiation is determined as a measure of photocatalytic activity. Dependence between photocatalytic activity and SiO2 content in the composite is determined. Rate constant k is found dependent on the content of SiO2 in the composite that calcined at 900 oC. The addition of low composition SiO2 to the TiO2 matrix (lower than 45% enhances the photocatalytic activity due to thermal stability and increasing in the surface area. The effects of chemical compositions on the surface topography and the crystallization of phases are studied.

  11. Application of hydrothermally produced TiO{sub 2} nanotubes in photocatalytic esterification of oleic acid

    Energy Technology Data Exchange (ETDEWEB)

    Manique, Márcia Cardoso, E-mail: marciamanique@yahoo.com.br; Silva, Aline Posteral; Alves, Annelise Kopp; Bergmann, Carlos Pérez

    2016-04-15

    Highlights: • A hydrothermal method was employed to synthesize TiO{sub 2} nanotubes. • TiO{sub 2} nanotubes were studied for photocatalytic esterification of oleic acid. • Optimum conditions were obtained at a concentration of 15% (w/w) and a molar ratio 3:1 (methanol:oleic acid). • The greater number of hydroxyl groups may have contributed to a low yield of ester versus P25. - Abstract: This study investigated the use of TiO{sub 2} nanotubes (TNTs) as photocatalysts in the esterification of fatty acids for biodiesel production. The TNTs were synthesized via a hydrothermal route and evaluated for their crystallinity, morphology, surface area and photocatalytic activity compared with a TiO{sub 2} P25 standard. Optimum photocatalytic conditions were obtained using a 15% concentration of catalyst (w/w) and a 3:1 molar ratio of methanol to oleic acid. The highest yield of methyl oleate obtained was 86.0% when P25 was used as a photocatalyst. The lowest band gap energy was obtained with the TNT sample synthesized at 110 °C for 48 h (E{sub g} = 3.08 eV), which also exhibited the highest rate of oleic acid esterification (59.3%) among all the investigated TNTs. We also observed that, in addition to the band gap, other factors such as the crystalline phase of the TNTs and their surface area were important in photocatalytic performance.

  12. Synthesis of hexagonal ultrathin tungsten oxide nanowires with diameters below 5 nm for enhanced photocatalytic performance

    Science.gov (United States)

    Lu, Huidan; Zhu, Qin; Zhang, Mengying; Yan, Yi; Liu, Yongping; Li, Ming; Yang, Zhishu; Geng, Peng

    2018-04-01

    Semiconductor with one dimension (1D) ultrathin nanostructure has been proved to be a promising nanomaterial in photocatalytic field. Great efforts were made on preparation of monoclinic ultrathin tungsten oxide nanowires. However, non-monoclinic phase tungsten oxides with 1D ultrathin structure, especially less than 5 nm width, have not been reported. Herein, we report the synthesis of hexagonal ultrathin tungsten oxide nanowires (U-WOx NW) by modified hydrothermal method. Microstructure characterization showed that U-WOx NW have the diameters of 1-3 nm below 5 nm and are hexagonal phase sub-stoichiometric WOx. U-WOx NW show absorption tail in the visible and near infrared region due to oxygen vacancies. For improving further photocatalytic performance, Ag co-catalyst was grown directly onto U-WOx NW surface by in situ redox reaction. Photocatalytic measurements revealed hexagonal U-WOx NW have better photodegradation activity, compared with commercial WO3(C-WO3) and oxidized U-WOx NW, ascribe to larger surface area, short diffusion length of photo-generated charge carriers and visible absorption of oxygen-vacancy-rich hexagonal ultrathin nanostructures. Moreover, the photocatalytic activity and stability of U-WOx NW using Ag co-catalyst were further improved.

  13. TiO{sub 2}-based nanotubes modified with nickel: synthesis, properties, and improved photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Qamar, M; Ganguli, A K [Department of Chemistry, Indian Institute of Technology, Hauz Khas, New Delhi 110016 (India); Kim, S J, E-mail: sjkim1@sejong.ac.k, E-mail: ashok@chemistry.iitd.ac.i [Department of Nano Science and Technology, Sejong Advanced Institute of Nano Technologies, Sejong University, 98, Gunja-dong, Gwangjin-gu, Seoul 143-747 (Korea, Republic of)

    2009-11-11

    Titanate nanotubes containing 2.5 wt% Ni were synthesized from TiO{sub 2} sol using alkali hydrothermal treatment followed by a simple ion-exchange process. The changes in phase, shape and morphology, surface area, and photocatalytic activity of these nanotubes have been explored as a function of calcination temperature. The samples were characterized using standard techniques, including x-ray diffraction, transmission electron microscopy, scanning electron microscopy, inductively coupled plasma spectrometry, energy dispersive x-ray spectroscopy, and Brauner-Emmett-Teller surface area analysis. The study revealed that the titanate phase containing Ni ions can be converted to the anatase phase after certain heat treatments but, at the same time, the tubular morphology was partially lost. Investigation of photocatalytic properties demonstrated that the as-prepared Ni-titanate nanotubes were photocatalytically inactive, but when heated at temperatures below 500 {sup 0}C their activity was significantly enhanced with the change in phase. The calcined nanotube samples carrying nickel ion showed better photocatalytic activity than calcined nanotube samples containing protons. The hydrogen adsorption capacity of these titanates has also been measured, and it was found that Ni-titanate nanotubes can adsorb more hydrogen than its counterpart Na-titanate.

  14. TiO2-Based Photocatalytic Geopolymers for Nitric Oxide Degradation

    Science.gov (United States)

    Strini, Alberto; Roviello, Giuseppina; Ricciotti, Laura; Ferone, Claudio; Messina, Francesco; Schiavi, Luca; Corsaro, Davide; Cioffi, Raffaele

    2016-01-01

    This study presents an experimental overview for the development of photocatalytic materials based on geopolymer binders as catalyst support matrices. Particularly, geopolymer matrices obtained from different solid precursors (fly ash and metakaolin), composite systems (siloxane-hybrid, foamed hybrid), and curing temperatures (room temperature and 60 °C) were investigated for the same photocatalyst content (i.e., 3% TiO2 by weight of paste). The geopolymer matrices were previously designed for different applications, ranging from insulating (foam) to structural materials. The photocatalytic activity was evaluated as NO degradation in air, and the results were compared with an ordinary Portland cement reference. The studied matrices demonstrated highly variable photocatalytic performance depending on both matrix constituents and the curing temperature, with promising activity revealed by the geopolymers based on fly ash and metakaolin. Furthermore, microstructural features and titania dispersion in the matrices were assessed by scanning electron microscopy (SEM) and energy dispersive X-ray (EDS) analyses. Particularly, EDS analyses of sample sections indicated segregation effects of titania in the surface layer, with consequent enhancement or depletion of the catalyst concentration in the active sample region, suggesting non-negligible transport phenomena during the curing process. The described results demonstrated that geopolymer binders can be interesting catalyst support matrices for the development of photocatalytic materials and indicated a large potential for the exploitation of their peculiar features. PMID:28773634

  15. TiO2-Based Photocatalytic Geopolymers for Nitric Oxide Degradation

    Directory of Open Access Journals (Sweden)

    Alberto Strini

    2016-06-01

    Full Text Available This study presents an experimental overview for the development of photocatalytic materials based on geopolymer binders as catalyst support matrices. Particularly, geopolymer matrices obtained from different solid precursors (fly ash and metakaolin, composite systems (siloxane-hybrid, foamed hybrid, and curing temperatures (room temperature and 60 °C were investigated for the same photocatalyst content (i.e., 3% TiO2 by weight of paste. The geopolymer matrices were previously designed for different applications, ranging from insulating (foam to structural materials. The photocatalytic activity was evaluated as NO degradation in air, and the results were compared with an ordinary Portland cement reference. The studied matrices demonstrated highly variable photocatalytic performance depending on both matrix constituents and the curing temperature, with promising activity revealed by the geopolymers based on fly ash and metakaolin. Furthermore, microstructural features and titania dispersion in the matrices were assessed by scanning electron microscopy (SEM and energy dispersive X-ray (EDS analyses. Particularly, EDS analyses of sample sections indicated segregation effects of titania in the surface layer, with consequent enhancement or depletion of the catalyst concentration in the active sample region, suggesting non-negligible transport phenomena during the curing process. The described results demonstrated that geopolymer binders can be interesting catalyst support matrices for the development of photocatalytic materials and indicated a large potential for the exploitation of their peculiar features.

  16. One stone, two birds: silica nanospheres significantly increase photocatalytic activity and colloidal stability of photocatalysts

    Science.gov (United States)

    Rasamani, Kowsalya D.; Foley, Jonathan J., IV; Sun, Yugang

    2018-03-01

    Silver-doped silver chloride [AgCl(Ag)] nanoparticles represent a unique class of visible-light-driven photocatalysts, in which the silver dopants introduce electron-abundant mid-gap energy levels to lower the bandgap of AgCl. However, free-standing AgCl(Ag) nanoparticles, particularly those with small sizes and large surface areas, exhibit low colloidal stability and low compositional stability upon exposure to light irradiation, leading to easy aggregation and conversion to metallic silver and thus a loss of photocatalytic activity. These problems could be eliminated by attaching the small AgCl(Ag) nanoparticles to the surfaces of spherical dielectric silica particles with submicrometer sizes. The high optical transparency in the visible spectral region (400-800 nm), colloidal stability, and chemical/electronic inertness displayed by the silica spheres make them ideal for supporting photocatalysts and significantly improving their stability. The spherical morphology of the dielectric silica particles can support light scattering resonances to generate significantly enhanced electric fields near the silica particle surfaces, on which the optical absorption cross-section of the AgCl(Ag) nanoparticles is dramatically increased to promote their photocatalytic activity. The hybrid silica/AgCl(Ag) structures exhibit superior photocatalytic activity and stability, suitable for supporting photocatalysis sustainably; for instance, their efficiency in the photocatalytic decomposition of methylene blue decreases by only ˜9% even after ten cycles of operation.

  17. Heterojunction BiOI/Bi2MoO6 nanocomposite with much enhanced photocatalytic activity

    International Nuclear Information System (INIS)

    Li, Wen Ting; Zheng, Yi Fan; Yin, Hao Yong; Song, Xu Chun

    2015-01-01

    BiOI/Bi 2 MoO 6 heterostructures with different amounts of BiOI were successfully prepared via a facile deposition method. The obtained BiOI/Bi 2 MoO 6 photocatalysts exhibited much higher visible light (λ > 420 nm) induced photocatalytic activity compared with single Bi 2 MoO 6 and BiOI photocatalysts. 20 % BiOI/Bi 2 MoO 6 nanocomposite exhibited the highest photocatalytic activity with almost all RhB decomposed within 70 min. However, excess BiOI covering on the surface of Bi 2 MoO 6 can inversely reduce the photocatalytic activity. The enhanced photocatalytic activities could be resulted from the function of the novel p–n heterojunction interface between Bi 2 MoO 6 and BiOI, which could separate photoinduced carriers efficiently. Possible mechanisms on the basis of the relative band positions were also discussed

  18. Increased photocatalytic activity induced by TiO2/Pt/SnO2 heterostructured films

    Science.gov (United States)

    Testoni, Glaucio O.; Amoresi, Rafael A. C.; Lustosa, Glauco M. M. M.; Costa, João P. C.; Nogueira, Marcelo V.; Ruiz, Miguel; Zaghete, Maria A.; Perazolli, Leinig A.

    2018-02-01

    In this work, a high photocatalytic activity was attained by intercalating a Pt layer between SnO2 and TiO2 semiconductors, which yielded a TiO2/Pt/SnO2 - type heterostructure used in the discoloration of blue methylene (MB) solution. The porous films and platinum layer were obtained by electrophoretic deposition and DC Sputtering, respectively, and were both characterized morphologically and structurally by FE-SEM and XRD. The films with the Pt interlayer were evaluated by photocatalytic activity through exposure to UV light. An increase in efficiency of 22% was obtained for these films compared to those without platinum deposition. Studies on the reutilization of the films pointed out high efficiency and recovery of the photocatalyst, rendering the methodology favorable for the construction of fixed bed photocatalytic reactors. A proposal associated with the mechanism is discussed in this work in terms of the difference in Schottky barrier between the semiconductors and the electrons transfer and trapping cycle. These are fundamental factors for boosting photocatalytic efficiency.

  19. Photocatalytic degradation of paraoxon-ethyl in aqueous solution using titania nanoparticulate film

    Energy Technology Data Exchange (ETDEWEB)

    Prasad, G.K., E-mail: gkprasad2001@yahoo.com; Ramacharyulu, P.V.R.K.; Kumar, J. Praveen; Srivastava, A.R.; Singh, Beer

    2012-06-30

    Photocatalytic degradation of paraoxon-ethyl (o,o-diethyl o-(4-nitrophenyl) phosphate), a well known surrogate of chemical warfare agents, in aqueous solution was studied by using titania nanoparticulate film. Reaction followed pseudo first order behaviour. Photolytic degradation reaction of paraoxon-ethyl demonstrated relatively low rate with a value of rate constant of 2.5 Multiplication-Sign 10{sup -3} min{sup -1}. Whereas, degradation reaction in the presence of titania nanoparticulate film and UV light displayed enhanced rate with a value of rate constant of 6.9 Multiplication-Sign 10{sup -3} min{sup -1} due to photocatalysis. Gas chromatography-mass spectrometry analysis showed the formation of p-nitrophenol, o,o-diethyl phosphonic acid, o-ethyl, diphosphonic acid, phosphoric acid, dimerized product of o,o-diethyl phosphonic acid, acetaldehyde, and carbon dioxide due to photocatalytic degradation of paraoxon-ethyl. It indicates that, photocatalytic degradation reaction begins with destruction of P-O-C bonds. Subsequently, P, C atoms were found to be oxidized gradually, and contributed to its photocatalytic degradation. - Highlights: Black-Right-Pointing-Pointer Synthesis of titania nanoparticles by sol-gel method. Black-Right-Pointing-Pointer Fabrication of titania nanoparticulate film by dip coating. Black-Right-Pointing-Pointer Paraoxon ethyl degradation reactions followed pseudo first order behaviour. Black-Right-Pointing-Pointer Paraoxon-ethyl degraded to non toxic compounds like CO{sub 2}, acetaldehyde, and nitrophenol.

  20. Cyclohexane selective photocatalytic oxidation by anatase TiO2: influence of particle size and crystallinity

    NARCIS (Netherlands)

    Carneiro, J.T.; Carneiro, Joana T.; Almeida, A.R.; Almeida, Ana R.; Moulijn, Jacob A.; Mul, Guido

    2010-01-01

    A systematic study is presented on the effect of crystallite size of Anatase (Hombikat, Sachtleben), varied by calcination at different temperatures up to 800 °C, on photocatalytic activity in cyclohexane selective oxidation. Two different reactors were used to test the materials: a top illumination