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Sample records for catalytic hydrogen production

  1. Catalytic glycerol steam reforming for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Dan, Monica, E-mail: monica.dan@itim-cj.ro; Mihet, Maria, E-mail: maria.mihet@itim-cj.ro; Lazar, Mihaela D., E-mail: diana.lazar@itim-cj.ro [National Institute for Research and Development of Isotopic and Molecular Technologies, 67-103 Donat Street, 400293 Cluj Napoca (Romania)

    2015-12-23

    Hydrogen production from glycerol by steam reforming combine two major advantages: (i) using glycerol as raw material add value to this by product of bio-diesel production which is obtained in large quantities around the world and have a very limited utilization now, and (ii) by implication of water molecules in the reaction the efficiency of hydrogen generation is increased as each mol of glycerol produces 7 mol of H{sub 2}. In this work we present the results obtained in the process of steam reforming of glycerol on Ni/Al{sub 2}O{sub 3}. The catalyst was prepared by wet impregnation method and characterized through different methods: N{sub 2} adsorption-desorption, XRD, TPR. The catalytic study was performed in a stainless steel tubular reactor at atmospheric pressure by varying the reaction conditions: steam/carbon ratio (1-9), gas flow (35 ml/min -133 ml/min), temperature (450-650°C). The gaseous fraction of the reaction products contain: H{sub 2}, CH{sub 4}, CO, CO{sub 2}. The optimum reaction conditions as resulted from this study are: temperature 550°C, Gly:H{sub 2}O ratio 9:1 and Ar flow 133 ml/min. In these conditions the glycerol conversion to gaseous products was 43% and the hydrogen yield was 30%.

  2. Catalytic glycerol steam reforming for hydrogen production

    Science.gov (United States)

    Dan, Monica; Mihet, Maria; Lazar, Mihaela D.

    2015-12-01

    Hydrogen production from glycerol by steam reforming combine two major advantages: (i) using glycerol as raw material add value to this by product of bio-diesel production which is obtained in large quantities around the world and have a very limited utilization now, and (ii) by implication of water molecules in the reaction the efficiency of hydrogen generation is increased as each mol of glycerol produces 7 mol of H2. In this work we present the results obtained in the process of steam reforming of glycerol on Ni/Al2O3. The catalyst was prepared by wet impregnation method and characterized through different methods: N2 adsorption-desorption, XRD, TPR. The catalytic study was performed in a stainless steel tubular reactor at atmospheric pressure by varying the reaction conditions: steam/carbon ratio (1-9), gas flow (35 ml/min -133 ml/min), temperature (450-650°C). The gaseous fraction of the reaction products contain: H2, CH4, CO, CO2. The optimum reaction conditions as resulted from this study are: temperature 550°C, Gly:H2O ratio 9:1 and Ar flow 133 ml/min. In these conditions the glycerol conversion to gaseous products was 43% and the hydrogen yield was 30%.

  3. Hydrogen production via catalytic processing of renewable feedstocks

    Energy Technology Data Exchange (ETDEWEB)

    Nazim Muradov; Franklyn Smith; Ali T-Raissi [Florida Solar Energy Center, University of Central Florida, Cocoa, Florida, (United States)

    2006-07-01

    Landfill gas (LFG) and biogas can potentially become important feedstocks for renewable hydrogen production. The objectives of this work were: (1) to develop a catalytic process for direct reforming of CH{sub 4}-CO{sub 2} gaseous mixture mimicking LFG, (2) perform thermodynamic analysis of the reforming process using AspenPlus chemical process simulator, (3) determine operational conditions for auto-thermal (or thermo-neutral) reforming of a model CH{sub 4}-CO{sub 2} feedstock, and (4) fabricate and test a bench-scale hydrogen production unit. Experimental data obtained from catalytic reformation of the CH{sub 4}-CO{sub 2} and CH{sub 4}-CO{sub 2}-O{sub 2} gaseous mixtures using Ni-catalyst were in a good agreement with the simulation results. It was demonstrated that catalytic reforming of LFG-mimicking gas produced hydrogen with the purity of 99.9 vol.%. (authors)

  4. Hydrogen production by catalytic partial oxidation of methane

    OpenAIRE

    Enger, Bjørn Christian

    2008-01-01

    Hydrogen production by catalytic partial oxidation of natural gas was investigated using tools ranging from theoretical calculations to experimental work and sophisticated characterization techniques.Catalytic partial oxidation (CPO) was carried out in a conventional continuous flow experimental apparatus using a xed-bed reactor, and operating at 1 atm and furnace temperatures in the range from ambient to 1073 K. The feed typically consisted of a mixture of methane and air, with a CH4/O2 rati...

  5. Cobaloxime-based photo-catalytic devices for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Fihri, A.; Artero, V.; Razavet, M.; Baffert, C.; Fontecave, M. [CEA Grenoble, DSV, iRTSV, Lab Chim et Biol Metaux, CNRS, UMR 5249, Univ Grenoble 1, F-38054 Grenoble 9 (France); Leibl, W. [CEA, DSV, iBiTecS, Lab Photocatalyse et Biohydrogene, CNRS, URA 2096, Gif Sur Yvette (France)

    2008-07-01

    In this paper is described the synthesis and activity of a series of novel hetero-dinuclear ruthenium-cobaloxime photo-catalysts able to achieve the photochemical production of hydrogen with the highest turnover numbers so far reported for such devices. First of all, substituting cobalt for rare and expensive platinum, palladium, or rhodium metals in photo-catalysts is a first step toward economically viable hydrogen production. Cobaloximes appear to be good candidates for H{sub 2}-evolving catalysts, and they may provide a good basis for the design of photo-catalysts that function in pure water as both the solvent and the sustainable proton source. Secondly, a molecular connection between the sensitizer and the H{sub 2}-evolving catalyst seems to provide advantages regarding the photo-catalytic activity. Structural modifications of this connection should allow a better tuning of the electron transfer between the light-harvesting unit and the catalytic center and thus an increase of the efficiency of the system. (O.M.)

  6. Hydrogen production from methane through catalytic partial oxidation reactions

    Science.gov (United States)

    Freni, S.; Calogero, G.; Cavallaro, S.

    This paper reviews recent developments in syn-gas production processes used for partial methane oxidation with and/or without steam. In particular, we examined different process charts (fixed bed, fluidised bed, membrane, etc.), kinds of catalysts (powders, foams, monoliths, etc.) and catalytically active phases (Ni, Pt, Rh, etc.). The explanation of the various suggested technical solutions accounted for the reaction mechanism that may selectively lead to calibrated mixtures of CO and H 2 or to the unwanted formation of products of total oxidation (CO 2 and H 2O) and pyrolysis (coke). Moreover, the new classes of catalysts allow the use of small reactors to treat large amounts of methane (monoliths) or separate hydrogen in situ from the other reaction products (membrane). This leads to higher conversions and selectivity than could have been expected thermodynamically. Although catalysts based on Rh are extremely expensive, they can be used to minimise H 2O formation by maximising H 2 yield.

  7. Hydrogen production by catalytic gasification of cellulose in supercritical water

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Cellulose,one of the important components of biomass,was gasified in supercritical water to produce hydrogen-rich gas in an autoclave which was operated batch-wise under high-pressure.K2CO3 and Ca(OH)2 were selected as the catalysts (or promoters).The temperature was kept between 450℃ and 500℃ while pressure was maintained at 24-26 MPa.The reaction time was 20 min.Experimental results showed that the two catalysts had good catalytic effect and optimum amounts were observed for each catalyst.When 0.2 g K2CO3 was added,the hydrogen yield could reach 9.456 mol.kg-1 which was two times of the H2 amount produced without catalyst.When 1.6 g Ca(OH)2 was added,the H2 yield was K2CO3 as catalyst but is still 1.7 times that achieved without catalyst.Comparing with the results obtained using KaCO3 or Ca(OH)2 alone,the use of a combination of K2CO3 and Ca(OH)2 could increase the H2 yield by up to 2.5 times that without catalyst and 25% and 45% more than that obtained using K2CO3 and Ca(OH)2 alone,respectively.It was found that methane was the dominant product at relatively low temperature.When the temperature was increased,the methane reacts with water and is converted to hydrogen and carbon dioxide.

  8. Catalytic membrane reactors based on macroporous silicon for hydrogen production

    OpenAIRE

    Vega Bru, Didac; Hernández Díaz, David; López, E. (Eduardo); Jiménez, Nuria; Todorov Trifonov, Trifon; Rodríguez Martínez, Ángel; Alcubilla González, Ramón; Llorca Piqué, Jordi

    2010-01-01

    The typology of using hydrogen as an energy carrier and its implementation in portable fuel cells has motivated a considerable research interest in the development of new efficient hydrogen production technologies. Hydrogen storage and manipulation is however a problematic and hazardous issue. Therefore, the low temperature on-site steam reforming of alcohols for hydrogen supply offers a nice solution to safety and storage issues, while providing several environment advantages […] Peer Rev...

  9. Hydrogen production by catalytic partial oxidation of methane

    Energy Technology Data Exchange (ETDEWEB)

    Enger, Bjoern Christian

    2008-12-15

    Hydrogen production by catalytic partial oxidation of natural gas was investigated using tools ranging from theoretical calculations to experimental work and sophisticated characterization techniques. Catalytic partial oxidation (CPO) was carried out in a conventional continuous flow experimental apparatus using a fixed-bed reactor, and operating at 1 atm and furnace temperatures in the range from ambient to 1073 K. The feed typically consisted of a mixture of methane and air, with a CH{sub 4}/O{sub 2} ratio of 2, and the average bed residence time was in the range 10-250 ms. Steam methane reforming (SMR) was carried out in the same apparatus at similar temperatures and pressure in a feed consisting of methane, nitrogen and water, with a steam to carbon ratio of 2.0-4.0. Temperature programmed (TP) techniques, including oxidation (TPO), reduction (TPR), reaction (TPCPO) and methane dissociation (TPMD) was used to characterize catalytic properties such as ignition temperatures, the catalyst reducibility and activation energies. Dispersions from catalyst surface area measurements were compared to X-ray diffraction (XRD) techniques and electron microscopy (SEM, TEM,STEM) to obtain information on catalyst particle sizes and dispersion. X-ray photoelectron spectroscopy (XPS) provided information on the specific catalyst surface composition, which was compared to results on the bulk structure obtained by XRD. The effect of modifying cobalt catalysts supported on alumina was investigated by adding small amounts of Ni, Fe, Cr, Re, Mn, W, Mo, V and Ta oxides. The idea behind this work was to investigate whether the cobalt crystals were decorated, covered or encircled by a modifier and to what extent this affected catalyst performance. The choice of modifiers in this study was based on the principle that in any chemical process it may be just as important to identify groups of elements that have negative effects as identifying the best promoters. It was found that the

  10. HYDROGEN TRANSFER IN CATALYTIC CRACKING

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Hydrogen transfer is an important secondary reaction of catalytic cracking reactions, which affects product yield distribution and product quality. It is an exothermic reaction with low activation energy around 43.3 kJ/mol. Catalyst properties and operation parameters in catalytic cracking greatly influence the hydrogen transfer reaction. Satisfactory results are expected through careful selection of proper catalysts and operation conditions.

  11. Maximizing renewable hydrogen production from biomass in a bio/catalytic refinery

    DEFF Research Database (Denmark)

    Westermann, Peter; Jørgensen, Betina; Lange, L.;

    2007-01-01

    Biological production of hydrogen from biomass by fermentative or photofermentative microorganisms has been described in numerous research articles and reviews. The major challenge of these techniques is the low yield from fermentative production, and the large reactor volumes necessary...... for photofermentative production. Due to these constraints biological hydrogen production from biomass has so far not been considered a significant source in most scenarios of a future hydrogen-based economy. In this review we briefly summarize the current state of art of biomass-based hydrogen production and suggest...... a combination of a biorefinery for the production of multiple fuels (hydrogen, ethanol, and methane) and chemical catalytic technologies which could lead to a yield of 10-12 mol hydrogen per mol glucose derived from biological waste products. Besides the high hydrogen yield, the advantage of the suggested...

  12. Tunable Molecular MoS2 Edge-Site Mimics for Catalytic Hydrogen Production.

    Science.gov (United States)

    Garrett, Benjamin R; Polen, Shane M; Click, Kevin A; He, Mingfu; Huang, Zhongjie; Hadad, Christopher M; Wu, Yiying

    2016-04-18

    Molybdenum sulfides represent state-of-the-art, non-platinum electrocatalysts for the hydrogen evolution reaction (HER). According to the Sabatier principle, the hydrogen binding strength to the edge active sites should be neither too strong nor too weak. Therefore, it is of interest to develop a molecular motif that mimics the catalytic sites structurally and possesses tunable electronic properties that influence the hydrogen binding strength. Furthermore, molecular mimics will be important for providing mechanistic insight toward the HER with molybdenum sulfide catalysts. In this work, a modular method to tune the catalytic properties of the S-S bond in MoO(S2)2L2 complexes is described. We studied the homogeneous electrocatalytic hydrogen production performance metrics of three catalysts with different bipyridine substitutions. By varying the electron-donating abilities, we present the first demonstration of using the ligand to tune the catalytic properties of the S-S bond in molecular MoS2 edge-site mimics. This work can shed light on the relationship between the structure and electrocatalytic activity of molecular MoS2 catalysts and thus is of broad importance from catalytic hydrogen production to biological enzyme functions.

  13. Catalytic combustor for hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Mercea, J.; Grecu, E.; Fodor, T.; Kreibik, S.

    1982-01-01

    The performance of catalytic combustors for hydrogen using platinum-supported catalysts is described. Catalytic plates of different sizes were constructed using fibrous and ceramic supports. The temperature distribution as well as the reaction efficiency as a function of the fuel input rate was determined, and a comparison between the performances of different plates is discussed.

  14. Efficient photothermal catalytic hydrogen production over nonplasmonic Pt metal supported on TiO2

    Science.gov (United States)

    Song, Rui; Luo, Bing; Jing, Dengwei

    2016-10-01

    Most of the traditional photocatalytic hydrogen productions were conducted under room temperature. In this work, we selected nonplasmonic Pt metal anchored on TiO2 nanoparticles with photothermal activity to explore more efficient hydrogen production technology over the whole solar spectrum. Photothermal experiments were carried out in a carefully designed top irradiated photocatalytic reactor that can withstand high temperature and relatively higher pressure. Four typical organic materials, i.e., methyl alcohol (MeOH), trielthanolamne (TEOA), formic acid (HCOOH) and glucose, were investigated. Formic acid, a typical hydrogen carrier, was found to show the best activity. In addition, the effects of different basic parameters such as sacrificial agent concentration and the temperature on the activity of hydrogen generation were systematically investigated for understanding the qualitative and quantitative effects of the photothermal catalytic reaction process. The hydrogen yields at 90 °C of the photothermal catalytic reaction with Pt/TiO2 are around 8.1 and 4.2 times higher than those of reactions carried out under photo or thermal conditions alone. We can see that the photothermal hydrogen yield is not the simple sum of the photo and thermal effects. This result indicated that the Pt/TiO2 nanoparticles can efficiently couple photo and thermal energy to more effectively drive hydrogen production. As a result, the excellent ability makes it superior to other conventional semiconductor photocatalysts and thermal catalysts. Future works could concentrate on exploring photothermal catalysis as well as the potential synergism between photo and thermal effects to find more efficient hydrogen production technology using the whole solar spectrum.

  15. Design, fabrication and testing of a catalytic microreactor for hydrogen production

    Science.gov (United States)

    Kim, Taegyu; Kwon, Sejin

    2006-09-01

    A catalytic microreactor for hydrogen production was fabricated by anisotropic wet etching of photosensitive glass, which enables it to be a structure with high tight tolerance and high aspect ratio. As a reactor structure, a microchannel was used for improving heat and mass transfer in the reactor. The primary fuel source is methanol for a mobile device. Endothermic catalytic steam reforming of methanol was chosen for producing gaseous hydrogen. The Cu-based catalyst, Cu/ZnO, was prepared by the co-precipitation method and coated on the surface of the microchannel for methanol steam reforming. An overall microfabrication process was established for a MEMS-based catalytic microreactor. The fabricated reactor has a volume of 1.8 cm3 including the volume of the reaction chamber 0.3 cm3 and produced dry reformate with high hydrogen content, 73%. The hydrogen flow was 4.16 ml min-1, which can generate a power output of 350 mWe for a fuel cell.

  16. Catalytic heat exchangers for small-scale production of hydrogen - feasibility study

    Energy Technology Data Exchange (ETDEWEB)

    Silversand, F. [Catator AB, Lund (Sweden)

    2002-02-01

    A feasibility study concerning heat-exchanger reactors in small-scale production of hydrogen has been performed on the request of Svenskt Gastekniskt Center AB and SWEP International AB. The basic idea is to implement different catalysts into brazed plate-type heat exchangers. This can be achieved by installing catalytic cylinders in the inlet-and outlet ports of the heat exchangers or through treatment of the plates to render them catalytically active. It is also possible to sandwich catalytically active wire meshes between the plates. Experiments concerning steam reforming of methanol and methane have been performed in a micro-reactor to gather kinetic data for modelling purposes. Performance calculations concerning heat exchanger reactors have then been conducted with Catator's generic simulation code for catalytic reactors (CatalystExplorer). The simulations clearly demonstrate the technical performance of these reactors. Indeed, the production rate of hydrogen is expected to be about 10 nm{sup 3}/h per litre of heat exchanger. The corresponding value for a conventional steam-reforming unit is about 1 nm{sup 3}/h or less per litre of reactor volume. Also, the compactness and the high degree of integration together with the possibilities of mass production will give an attractive cost for such units. Depending on the demands concerning the purity of the hydrogen it is possible to add secondary catalytic steps like water-gas shifters, methanation and selective oxidation, into a one-train unit, i.e. to design an all-inclusive design. Such reactors can be used for the supply of hydrogen to fuel cells. The production cost for hydrogen can be cut by 60 - 70% through the utilisation of heat exchanger reactors instead of conventional electrolysis. This result is primarily a result of the high price for electricity compared to the feed stock prices in steam reforming. It is important to verify the performance calculations and the simulation results through

  17. Hydrogen Production From Crude Bio-oil and Biomass Char by Electrochemical Catalytic Reforming

    Institute of Scientific and Technical Information of China (English)

    Xing-long Li; Shen Ning; Li-xia Yuan; Quan-xin Li

    2011-01-01

    We reports an efficient approach for production of hydrogen from crude bio-oil and biomass char in the dual fixed-bed system by using the electrochemical catalytic reforming method.The maximal absolute hydrogen yield reached 110.9 g H2/kg dry biomass.The product gas was a mixed gas containing 72%H2,26%CO2,1.9%CO,and a trace amount of CH4.It was observed that adding biomass char (a by-product of pyrolysis of biomass) could remarkably increase the absolute H2 yield (about 20%-50%).The higher reforming temperature could enhance the steam reforming reaction of organic compounds in crude bio-oil and the reaction of CO and H2O.In addition,the CuZn-Al2O3 catalyst in the water-gas shift bed could also increase the absolute H2 yield via shifting CO to CO2.

  18. Hydrogen Production From Crude Bio-oil and Biomass Char by Electrochemical Catalytic Reforming

    Science.gov (United States)

    Li, Xing-long; Ning, Shen; Yuan, Li-xia; Li, Quan-xin

    2011-08-01

    We reports an efficient approach for production of hydrogen from crude bio-oil and biomass char in the dual fixed-bed system by using the electrochemical catalytic reforming method. The maximal absolute hydrogen yield reached 110.9 g H2/kg dry biomass. The product gas was a mixed gas containing 72%H2, 26%CO2, 1.9%CO, and a trace amount of CH4. It was observed that adding biomass char (a by-product of pyrolysis of biomass) could remarkably increase the absolute H2 yield (about 20%-50%). The higher reforming temperature could enhance the steam reforming reaction of organic compounds in crude bio-oil and the reaction of CO and H2O. In addition, the CuZn-Al2O3 catalyst in the water-gas shift bed could also increase the absolute H2 yield via shifting CO to CO2.

  19. Hydrogen production by catalytic processing of renewable methane-rich gases

    Energy Technology Data Exchange (ETDEWEB)

    Muradov, Nazim; Smith, Franklyn; T-Raissi, Ali [Florida Solar Energy Center, University of Central Florida, Cocoa, FL 32922-5703 (United States)

    2008-04-15

    Biomass-derived methane-rich gases such as landfill gas (LFG), biogas and digester gas are promising renewable resources for near-future production of hydrogen. The technical and economical feasibility of hydrogen production via catalytic reforming of LFG and other methane-rich gases is evaluated in this paper. The thermodynamic equilibrium calculations and experimental measurements of reformation of methane-rich CH{sub 4}-CO{sub 2} mixtures over Ni-based catalyst were conducted. The problems associated with the catalyst deactivation due to carbon lay down and effects of steam and oxygen on the process sustainability were explored. Two technological approaches distinguished by the mode of heat input to the endothermic process (i.e., external vs autothermal) were modeled using AspenPlus trademark chemical process simulator and validated experimentally. A 5 kW{sub th} pilot unit for hydrogen production from LFG-mimicking CH{sub 4}-CO{sub 2} mixture was fabricated and operated. A preliminary techno-economic assessment indicates that the liquid hydrogen production costs are in the range of 3.00-7.00 per kilogram depending upon the plant capacity, the process heat input option and whether or not carbon sequestration is included in the process. (author)

  20. A resource recycling technique of hydrogen production from the catalytic degradation of organics in wastewater

    Institute of Scientific and Technical Information of China (English)

    LI XiaoNian; ZHANG QunFeng; KONG LingNiao; XIANG YiZhi; JU YaoMing; WU XiaoQiong; FENG Feng; YUAN JunFeng; MA Lei; LU ChunShan

    2008-01-01

    A resource recycling technique of hydrogen production from the catalytic degradation of organics in wastewater by aqueous phase reforming (APR) has been proposed. It is worthy of noting that this technique may be a potential way for the purification of refractory and highly toxic organics in water for hydrogen production. Hazardous organics (such as phenol, aniline, nitrobenzene, tetrahydrofuran (THF), toluene, N,N-dimethylformamide (DMF) and cyclohexanol) in water could be completely de-graded into H2 and CO2 with high selectivity over Raney Ni, and Sn-modified Raney Ni (Sn-Raney-Ni) or Pd/C catalyst under mild conditions. The experimental results operated in tubular and autoclave reactors, indicated that the degradation degree of organics and H2 selectivity could reach 100% under the optimal reaction conditions. The Sn-Raney-Ni (Sn/Ni=0.06) and Pd/C catalysts show better catalytic performances than the Raney Ni catalyst for the degradation of organics in water into H2 and CO2 by the aqueous phase reforming process.

  1. Co-production of hydrogen and carbon nanotubes on nickel foam via methane catalytic decomposition

    Science.gov (United States)

    Ping, Dan; Wang, Chaoxian; Dong, Xinfa; Dong, Yingchao

    2016-04-01

    The co-production of COx-free hydrogen and carbon nanotubes (CNTs) was achieved on 3-dimensional (3D) macroporous nickel foam (NF) via methane catalytic decomposition (MCD) over nano-Ni catalysts using chemical vapor deposition (CVD) technique. By a simple coating of a NiO-Al2O3 binary mixture sol followed by a drying-calcination-reduction treatment, NF supported composite catalysts (denoted as NiyAlOx/NF) with Al2O3 transition-layer incorporated with well-dispersed nano-Ni catalysts were successfully prepared. The effects of Ni loading, calcination temperature and reaction temperature on the performance for simultaneous production of COx-free hydrogen and CNTs were investigated in detail. Catalysts before and after MCD were characterized by XRD, TPR, SEM, TEM, TG and Raman spectroscopy technology. Results show that increasing Ni loading, lowering calcination temperature and optimizing MCD reaction temperature resulted in high production efficiency of COx-free H2 and carbon, but broader diameter distribution of CNTs. Through detailed parameter optimization, the catalyst with a Ni/Al molar ratio of 0.1, calcination temperature of 550 °C and MCD temperature of 650 °C was favorable to simultaneously produce COx-free hydrogen with a growth rate as high as 10.3% and CNTs with uniform size on NF.

  2. Production of natural antioxidants from vegetable oil deodorizer distillates: effect of catalytic hydrogenation.

    Science.gov (United States)

    Pagani, María Ayelén; Baltanás, Miguel A

    2010-02-01

    Natural tocopherols are one of the main types of antioxidants found in living creatures, but they also have other critical biological functions. The biopotency of natural (+)-alpha-tocopherol (RRR) is 36% higher than that of the synthetic racemic mixture and 300% higher than the SRR stereoisomer. Vegetable oil deodorizer distillates (DD) are an excellent source of natural tocopherols. Catalytic hydrogenation of DD preconcentrates has been suggested as a feasible route for recovery of tocopherols in high yield. However, it is important to know whether the hydrogenation operation, as applied to these tocopherol-rich mixtures, is capable of preserving the chiral (RRR) character, which is critical to its biopotency. Fortified (i.e., (+)-alpha-tocopherol enriched) sunflower oil and methyl stearate, as well as sunflower oil DD, were fully hydrogenated using commercial Ni and Pd catalysts (120-180 degrees C; 20-60 psig). Products were analyzed by chiral HPLC. Results show that the desired chiral configuration (RRR) is fully retained. Thus, the hydrogenation route can be safely considered as a valid alternative for increasing the efficiency of tocopherol recovery processes from DDs while preserving their natural characteristics.

  3. A novel liquid system of catalytic hydrogenation

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    On the basis that endothermic aqueous-phase reforming of oxygenated hydrocarbons for H2 production and exothermic liquid phase hydrogenation of organic compounds are carried out under extremely close conditions of temperature and pressure over the same type of catalyst, a novel liquid system of catalytic hydrogenation has been proposed, in which hydrogen produced from aqueous-phase reforming of oxygenated hydrocarbons is in situ used for liquid phase hydrogenation of organic compounds. The usage of active hydrogen generated from aqueous-phase reforming of oxygenated hydrocarbons for liquid catalytic hydrogenation of organic compounds could lead to increasing the selectivity to H2 in the aqueous-phase reforming due to the prompt removal of hydrogen on the active centers of the catalyst. Meanwhile, this novel liquid system of catalytic hydrogenation might be a potential method to improve the selectivity to the desired product in liquid phase catalytic hydrogenation of organic compounds. On the other hand, for this novel liquid system of catalytic hydrogenation, some special facilities for H2 generation, storage and transportation in traditional liquid phase hydrogenation industry process are yet not needed. Thus, it would simplify the working process of liquid phase hydrogenation and increase the energy usage and hydrogen productivity.

  4. Catalytic on-board hydrogen production from methanol and ammonia for mobile application

    Energy Technology Data Exchange (ETDEWEB)

    Soerijanto, H.

    2008-08-15

    This PhD thesis deals with the catalytic hydrogen production for mobile application, for example for the use in fuel cells for electric cars. Electric powered buses with fuel cells as driving system are well known, but the secure hydrogen storage in adequate amounts for long distance drive is still a topic of discussion. Methanol is an excellent hydrogen carrier. First of all it has a high H:C ratio and therefore a high energy density. Secondly the operating temperature of steam reforming of methanol is comparatively low (250 C) and there is no risk of coking since methanol has no C-C bond. Thirdly methanol is a liquid, which means that the present gasoline infrastructure can be used. For the further development of catalysts and for the construction of a reformer it is very important to characterize the catalysts very well. For the dimensioning and the control of an on-board production of hydrogen it is essential to draw accurately on the thermodynamic, chemical and kinetic data of the reaction. At the first part of this work the mesoporous Cu/ZrO{sub 2}/CeO{sub 2}-catalysts with various copper contents were characterized and their long-term stability and selectivity were investigated, and the kinetic data were determined. Carbon monoxide is generated by reforming of carbon containing material. This process is undesired since CO poisons the Pt electrode of the fuel cell. The separation of hydrogen by metal membranes is technically feasible and a high purity of hydrogen can be obtained. However, due to their high density this procedure is not favourable because of its energy loss. In this study a concept is presented, which enables an autothermal mode by application of ceramic membrane and simultaneously could help to deal with the CO problem. The search for an absolutely selective catalyst is uncertain. The production of CO can be neither chemically nor thermodynamically excluded, if carbon is present in the hydrogen carrier. Since enrichment or separation are

  5. 97e Intermediate Temperature Catalytic Reforming of Bio-Oil for Distributed Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Marda, J. R.; Dean, A. M.; Czernik, S.; Evans, R. J.; French, R.; Ratcliff, M.

    2008-01-01

    With the world's energy demands rapidly increasing, it is necessary to look to sources other than fossil fuels, preferably those that minimize greenhouse emissions. One such renewable source of energy is biomass, which has the added advantage of being a near-term source of hydrogen. While there are several potential routes to produce hydrogen from biomass thermally, given the near-term technical barriers to hydrogen storage and delivery, distributed technologies such that hydrogen is produced at or near the point of use are attractive. One such route is to first produce bio-oil via fast pyrolysis of biomass close to its source to create a higher energy-density product, then ship this bio-oil to its point of use where it can be reformed to hydrogen and carbon dioxide. This route is especially well suited for smaller-scale reforming plants located at hydrogen distribution sites such as filling stations. There is also the potential for automated operation of the conversion system. A system has been developed for volatilizing bio-oil with manageable carbon deposits using ultrasonic atomization and by modifying bio-oil properties, such as viscosity, by blending or reacting bio-oil with methanol. Non-catalytic partial oxidation of bio-oil is then used to achieve significant conversion to CO with minimal aromatic hydrocarbon formation by keeping the temperature at 650 C or less and oxygen levels low. The non-catalytic reactions occur primarily in the gas phase. However, some nonvolatile components of bio-oil present as aerosols may react heterogeneously. The product gas is passed over a packed bed of precious metal catalyst where further reforming as well as water gas shift reactions are accomplished completing the conversion to hydrogen. The approach described above requires significantly lower catalyst loadings than conventional catalytic steam reforming due to the significant conversion in the non-catalytic step. The goal is to reform and selectively oxidize the

  6. Effect of Catalytic Cylinders on Autothermal Reforming of Methane for Hydrogen Production in a Microchamber Reactor

    Directory of Open Access Journals (Sweden)

    Yunfei Yan

    2014-01-01

    Full Text Available A new multicylinder microchamber reactor is designed on autothermal reforming of methane for hydrogen production, and its performance and thermal behavior, that is, based on the reaction mechanism, is numerically investigated by varying the cylinder radius, cylinder spacing, and cylinder layout. The results show that larger cylinder radius can promote reforming reaction; the mass fraction of methane decreased from 26% to 21% with cylinder radius from 0.25 mm to 0.75 mm; compact cylinder spacing corresponds to more catalytic surface and the time to steady state is decreased from 40 s to 20 s; alteration of staggered and aligned cylinder layout at constant inlet flow rates does not result in significant difference in reactor performance and it can be neglected. The results provide an indication and optimize performance of reactor; it achieves higher conversion compared with other reforming reactors.

  7. Effect of catalytic cylinders on autothermal reforming of methane for hydrogen production in a microchamber reactor.

    Science.gov (United States)

    Yan, Yunfei; Guo, Hongliang; Zhang, Li; Zhu, Junchen; Yang, Zhongqing; Tang, Qiang; Ji, Xin

    2014-01-01

    A new multicylinder microchamber reactor is designed on autothermal reforming of methane for hydrogen production, and its performance and thermal behavior, that is, based on the reaction mechanism, is numerically investigated by varying the cylinder radius, cylinder spacing, and cylinder layout. The results show that larger cylinder radius can promote reforming reaction; the mass fraction of methane decreased from 26% to 21% with cylinder radius from 0.25 mm to 0.75 mm; compact cylinder spacing corresponds to more catalytic surface and the time to steady state is decreased from 40 s to 20 s; alteration of staggered and aligned cylinder layout at constant inlet flow rates does not result in significant difference in reactor performance and it can be neglected. The results provide an indication and optimize performance of reactor; it achieves higher conversion compared with other reforming reactors.

  8. Methane catalytic decomposition over ordered mesoporous carbons: A promising route for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Botas, J.A.; Serrano, D.P. [Department of Chemical and Environmental Technology, ESCET, Rey Juan Carlos University, c/ Tulipan s/n, 28933 Mostoles, Madrid (Spain); IMDEA Energia, c/Tulipan s/n, 28933 Mostoles, Madrid (Spain); Guil-Lopez, R.; Pizarro, P.; Gomez, G. [Department of Chemical and Environmental Technology, ESCET, Rey Juan Carlos University, c/ Tulipan s/n, 28933 Mostoles, Madrid (Spain)

    2010-09-15

    Methane decomposition offers an interesting route for the CO{sub 2}-free hydrogen production. The use of carbon catalysts, in addition to lowering the reaction temperature, presents a number of advantages, such as low cost, possibility of operating under autocatalytic conditions and feasibility of using the produced carbons in non-energy applications. In this work, a novel class of carbonaceous materials, having an ordered mesoporous structure (CMK-3 and CMK-5), has been checked as catalysts for methane decomposition, the results obtained being compared to those corresponding to a carbon black sample (CB-bp) and two activated carbons, presenting micro- (AC-mic) and mesoporosity (AC-mes), respectively. Ordered mesoporous carbons, and especially CMK-5, possess a remarkable activity and stability for the hydrogen production through that reaction. Under both temperature programmed and isothermal experiments, CMK-5 has shown to be a superior catalyst for methane decomposition than the AC-mic and CB-bp materials. Likewise, the catalytic activity of CMK-5 is superior to that of AC-mes in spite of the presence of mesoporosity and a high surface area in the latter. The remarkable stability of the CMK-5 catalyst is demonstrated by the high amount of carbon deposits that can be formed on this sample. This result has been assigned to the growth of the carbon deposits from methane decomposition towards the outer part of the catalyst particles, avoiding the blockage of the uniform mesopores present in CMK-5. Thus, up to 25 g of carbon deposits have been formed per gram of CMK-5, while the latter still retains a significant catalytic activity. (author)

  9. Catalytic Metal Free Production of Large Cage Structure Carbon Particles: A Candidate for Hydrogen Storage

    Science.gov (United States)

    Kimura, Yuki; Nuth, Joseph A., III; Ferguson, Frank T.

    2005-01-01

    We will demonstrate that carbon particles consisting of large cages can be produced without catalytic metal. The carbon particles were produced in CO gas as well as by introduction of 5% methane gas into the CO gas. The gas-produced carbon particles were able to absorb approximately 16.2 wt% of hydrogen. This value is 2.5 times higher than the 6.5 wt% goal for the vehicular hydrogen storage proposed by the Department of Energy in the USA. Therefore, we believe that this carbon particle is an excellent candidate for hydrogen storage for fuel cells.

  10. Production of hydrogen from biomass by catalytic steam reforming of fast pyrolysis oil

    Energy Technology Data Exchange (ETDEWEB)

    Czernik, S.; Wang, D.; Chornet, E. [National Renewable Energy Lab., Golden, CO (United States). Center for Renewable Chemical Technologies and Materials

    1998-08-01

    Hydrogen is the prototype of the environmentally cleanest fuel of interest for power generation using fuel cells and for transportation. The thermochemical conversion of biomass to hydrogen can be carried out through two distinct strategies: (a) gasification followed by water-gas shift conversion, and (b) catalytic steam reforming of specific fractions derived from fast pyrolysis and aqueous/steam processes of biomass. This paper presents the latter route that begins with fast pyrolysis of biomass to produce bio-oil. This oil (as a whole or its selected fractions) can be converted to hydrogen via catalytic steam reforming followed by a water-gas shift conversion step. Such a process has been demonstrated at the bench scale using model compounds, poplar oil aqueous fraction, and the whole pyrolysis oil with commercial Ni-based steam reforming catalysts. Hydrogen yields as high as 85% have been obtained. Catalyst initial activity can be recovered through regeneration cycles by steam or CO{sub 2} gasification of carbonaceous deposits.

  11. Catalytic Ammonia Decomposition over High-Performance Ru/Graphene Nanocomposites for Efficient COx-Free Hydrogen Production

    Directory of Open Access Journals (Sweden)

    Gang Li

    2017-01-01

    Full Text Available Highly-dispersed Ru nanoparticles were grown on graphene nanosheets by simultaneously reducing graphene oxide and Ru ions using ethylene glycol (EG, and the resultant Ru/graphene nanocomposites were applied as a catalyst to ammonia decomposition for COx-free hydrogen production. Tuning the microstructures of Ru/graphene nanocomposites was easily accomplished in terms of Ru particle size, morphology, and loading by adjusting the preparation conditions. This was the key to excellent catalytic activity, because ammonia decomposition over Ru catalysts is structure-sensitive. Our results demonstrated that Ru/graphene prepared using water as a co-solvent greatly enhanced the catalytic performance for ammonia decomposition, due to the significantly improved nano architectures of the composites. The long-term stability of Ru/graphene catalysts was evaluated for COx-free hydrogen production from ammonia at high temperatures, and the structural evolution of the catalysts was investigated during the catalytic reactions. Although there were no obvious changes in the catalytic activities at 450 °C over a duration of 80 h, an aggregation of the Ru nanoparticles was still observed in the nanocomposites, which was ascribed mainly to a sintering effect. However, the performance of the Ru/graphene catalyst was decreased gradually at 500 °C within 20 h, which was ascribed mainly to both the effect of the methanation of the graphene nanosheet under a H2 atmosphere and to enhanced sintering under high temperatures.

  12. Investigation of products of low-temperature catalytic hydrogenization of Donbas coals

    Energy Technology Data Exchange (ETDEWEB)

    Osipov, A.M.; Osipov, K.D.; Chernyshova, M.I.; Petrik, G.K.

    1980-11-01

    The relationship of the composition and properties of primary products of low-temperature hydrogenation is presented in relation to the nature of the coal, of catalysts, and of the conditions of hydrogenation. Temperature, the nature of the catalysts and of the type of coal used were directly related to the content of methane, ethane, propane, and CO/sub 2/, and of hydrogen sulphide in the case of brown gaseous coals, as well as the dissolving of hydrogenates and asphaltene content. The structural composition of components dissolved in methylene chloride was determined by proton magnetic resonance. Results of the experiments indicated that lead chloride was the most promising catalyst for low-temperature hydrogenation.

  13. Experimental research on catalysts and their catalytic mechanism for hydrogen production by gasification of peanut shell in supercritical water

    Institute of Scientific and Technical Information of China (English)

    PEI Aixia; GUO Liejin; JIN Hui

    2007-01-01

    Peanut shell,mixed with sodium carboxymethylcellulose,was gasified at a temperature of 450℃ and a pressure range from 24 to 27 MPa with the presence of different catalysts,including K2CO3,ZnCl2 and Raney-Ni.The experimental results show that different catalysts have greatly different effects on the reaction.Gasification efficiency (GE),hydrogen gasification efficiency (GHE),carbon gasification efficiency (GCE),yield of hydrogen production (YH2) and potential yield of hydrogen production (YPH2) are applied to describe the catalytic efficiency.From the result of gaseous components,ZnCl2 has the highest hydrogen selectivity,K2CO3 is lower,and Raney-Ni is the lowest,but Raney-Ni is the most favorable to gasify biomass among the three catalysts,and its GE,GHE,GcE reach 126.84%,185.71%,94.24%,respectively.As expected,hydrogen selectivity increased and CH4 reduced rapidly when the mixture of ZnCl2 and Raney-Ni is used under the same condition.The optimization mixture appeared when 0.2 g of ZnCl2 was added to 1 g of Raney-Ni,43.56 g·kg-1 of hydrogen production was obtained.In addition,the catalytic mechanisms of different catalysts were analyzed,and the possible reaction pathway was brought forward,which helped to explain the experiment phenomena and results correctly.

  14. Polarographic catalytic wave of hydrogen--Parallel catalytic hydrogen wave of bovine serum albumin in thepresence of oxidants

    Institute of Scientific and Technical Information of China (English)

    GUO; Wei(过玮); LIU; Limin(刘利民); LIN; Hong(林洪); SONG; Junfeng(宋俊峰)

    2002-01-01

    A polarographic catalytic hydrogen wave of bovine serum albumin (BSA) at about -1.80 V (vs. SCE) in NH4Cl-NH3@H2O buffer is further catalyzed by such oxidants as iodate, persulfate and hydrogen peroxide, producing a kinetic wave. Studies show that the kinetic wave is a parallel catalytic wave of hydrogen, which resulted from that hydrogen ion is electrochemically reduced and chemically regenerated through oxidation of its reduction product, atomic hydrogen, by oxidants mentioned above. It is a new type of poralographic catalytic wave of protein, which is suggested to be named as a parallel catalytic hydrogen wave.

  15. Thermo-Catalytic Methane Decomposition for Hydrogen Production: Effect of Palladium Promoter on Ni-based Catalysts

    Directory of Open Access Journals (Sweden)

    Irene Lock Sow Mei

    2016-08-01

    Full Text Available Hydrogen production from the direct thermo-catalytic decomposition of methane is a promising alternative for clean fuel production. However, thermal decomposition of methane can hardly be of any practical and empirical interest in the industry unless highly efficient and effective catalysts, in terms of both catalytic activity and operational lifetime have been developed. In this study, the effect of palladium (Pd as a promoter onto Ni supported on alumina catalyst has been investigated by using co-precipitation technique. The introduction of Pd promotes better catalytic activity, operational lifetime and thermal stability of the catalyst. As expected, highest methane conversion was achieved at reaction temperature of 800 °C while the bimetallic catalyst (1 wt.% Ni -1wt.% Pd/Al2O3 gave the highest methane conversion of 70% over 15 min of time-on-stream (TOS. Interestingly, the introduction of Pd as promoter onto Ni-based catalyst also has a positive effect on the operational lifetime and thermal stability of the catalyst as the methane conversion has improved significantly over 240 min of TOS. Copyright © 2016 BCREC GROUP. All rights reserved Received: 21st January 2016; Revised: 6th February 2016; Accepted: 6th March 2016 How to Cite: Mei, I.L.S., Lock, S.S.M., Vo, D.V.N., Abdullah, B. (2016. Thermo-Catalytic Methane Decomposition for Hydrogen Production: Effect of Palladium Promoter on Ni-based Catalysts. Bulletin of Chemical Reaction Engineering & Catalysis, 11 (2: 191-199 (doi:10.9767/bcrec.11.2.550.191-199 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.11.2.550.191-199

  16. Highly active metastable ruthenium nanoparticles for hydrogen production through the catalytic hydrolysis of ammonia borane.

    Science.gov (United States)

    Abo-Hamed, Enass K; Pennycook, Timothy; Vaynzof, Yana; Toprakcioglu, Chris; Koutsioubas, Alexandros; Scherman, Oren A

    2014-08-13

    Late transition metal nanoparticles (NPs) with a favorably high surface area to volume ratio have garnered much interest for catalytic applications. Yet, these NPs are prone to aggregation in solution, which has been mitigated through attachment of surface ligands, additives or supports; unfortunately, protective ligands can severely reduce the effective surface area on the NPs available for catalyzing chemical transformations. The preparation of 'metastable' NPs can readily address these challenges. We report herein the first synthesis of monodisperse metastable ruthenium nanoparticles (RuNPs), having sub 5 nm size and an fcc structure, in aqueous media at room temperature, which can be stored for a period of at least 8 months. The RuNPs can subsequently be used for the catalytic, quantitative hydrolysis of ammonia-borane (AB) yielding hydrogen gas with 21.8 turnovers per min at 25 °C. The high surface area available for hydrolysis of AB on the metastable RuNPs translated to an Ea of 27.5 kJ mol(-1) , which is notably lower than previously reported values for RuNP based catalysts.

  17. Hydrogen peroxide catalytic decomposition

    Science.gov (United States)

    Parrish, Clyde F. (Inventor)

    2010-01-01

    Nitric oxide in a gaseous stream is converted to nitrogen dioxide using oxidizing species generated through the use of concentrated hydrogen peroxide fed as a monopropellant into a catalyzed thruster assembly. The hydrogen peroxide is preferably stored at stable concentration levels, i.e., approximately 50%-70% by volume, and may be increased in concentration in a continuous process preceding decomposition in the thruster assembly. The exhaust of the thruster assembly, rich in hydroxyl and/or hydroperoxy radicals, may be fed into a stream containing oxidizable components, such as nitric oxide, to facilitate their oxidation.

  18. APPRECIATION AND UTILIZATION OF LACTIC SUB-PRODUCTS: PROTEIN EXTRACTION AND CATALYTIC HYDROGENATION OF THE LACTOSE

    Directory of Open Access Journals (Sweden)

    Carlos Enrique Jeronimo

    2012-07-01

    Full Text Available The cheese-producing industry has in its production cycle to generate a product very rich in protein and lactose, called cheese whey. The waste currently has some food applications, but that does not add value to the real nutritional content and economical product that leverages. In order, therefore, a greater appreciation of cheese whey, studies were conducted for the recovery of proteins and the catalytic conversion of lactose into a polyol of high economic value, called lactitol. The results showed high removal efficiency of proteins in the order of 93% and the conversion of commercial lactose around 90% in 150 minutes of reaction. The applicability of whey, however, requires further testing to remove the chloride ions present in serum.

  19. Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    None

    2014-09-01

    This 2-page fact sheet provides a brief introduction to hydrogen production technologies. Intended for a non-technical audience, it explains how different resources and processes can be used to produce hydrogen. It includes an overview of research goals as well as “quick facts” about hydrogen energy resources and production technologies.

  20. Production of hydrogen, liquid fuels, and chemicals from catalytic processing of bio-oils

    Science.gov (United States)

    Huber, George W; Vispute, Tushar P; Routray, Kamalakanta

    2014-06-03

    Disclosed herein is a method of generating hydrogen from a bio-oil, comprising hydrogenating a water-soluble fraction of the bio-oil with hydrogen in the presence of a hydrogenation catalyst, and reforming the water-soluble fraction by aqueous-phase reforming in the presence of a reforming catalyst, wherein hydrogen is generated by the reforming, and the amount of hydrogen generated is greater than that consumed by the hydrogenating. The method can further comprise hydrocracking or hydrotreating a lignin fraction of the bio-oil with hydrogen in the presence of a hydrocracking catalyst wherein the lignin fraction of bio-oil is obtained as a water-insoluble fraction from aqueous extraction of bio-oil. The hydrogen used in the hydrogenating and in the hydrocracking or hydrotreating can be generated by reforming the water-soluble fraction of bio-oil.

  1. Hydrogen production by catalytic decomposition of methane using a Fe-based catalyst in a fluidized bed reactor

    Institute of Scientific and Technical Information of China (English)

    D.Torres; S.de Llobet; J.L.Pinilla; M.J.Lázaro; I.Suelves; R.Moliner

    2012-01-01

    Catalytic decomposition of methane using a Fe-based catalyst for hydrogen production has been studied in this work.A Fe/Al2O3 catalyst previously developed by our research group has been tested in a fluidized bed reactor (FBR).A parametric study of the effects of some process variables,including reaction temperature and space velocity,is undertaken.The operating conditions strongly affect the catalyst performance.Methane conversion was increased by increasing the temperature and lowering the space velocity.Using temperatures between 700 and 900 ℃ and space velocities between 3 and 6 LN/(gcat·h),a methane conversion in the range of 25%-40% for the gas exiting the reactor could be obtained during a 6 h run.In addition,carbon was deposited in the form of nanofilaments (chain like nanofibers and multiwall nanotubes) with similar properties to those obtained in a fixed bed reactor.

  2. Photo-catalytic hydrogen production over Fe{sub 2}O{sub 3} based catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Boudjemaa, A. [Technical and Scientific Research Centre of Physico-chemistry Analysis (CRAPC), BP 248, RP 16004, Algiers (Algeria); Laboratory of Chemistry of Natural Gas, Faculty of Chemistry (USTHB) BP 32, 16111 Algiers (Algeria); Trari, M. [Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry (USTHB) BP 32, 16111 Algiers (Algeria)

    2010-08-15

    The hydrogen photo-evolution was successfully achieved in aqueous (Fe{sub 1-x}Cr{sub x}){sub 2}O{sub 3} suspensions (0 {<=} x {<=} 1). The solid solution has been prepared by incipient wetness impregnation and characterized by X-ray diffraction, BET, transport properties and photo-electrochemistry. The oxides crystallize in the corundum structure, they exhibit n-type conductivity with activation energy of {proportional_to}0.1 eV and the conduction occurs via adiabatic polaron hops. The characterization of the band edges has been studied by the Mott Schottky plots. The onset potential of the photo-current is {proportional_to}0.2 V cathodic with respect to the flat band potential, implying a small existence of surface states within the gap region. The absorption of visible light promotes electrons into (Fe{sub 1-x}Cr{sub x}){sub 2}O{sub 3}-CB with a potential ({proportional_to}-0.5 V{sub SCE}) sufficient to reduce water into hydrogen. As expected, the quantum yield increases with decreasing the electro affinity through the substitution of iron by the more electropositive chromium which increases the band bending at the interface and favours the charge separation. The generated photo-voltage was sufficient to promote simultaneously H{sub 2}O reduction and SO{sub 3}{sup 2-} oxidation in the energetically downhill reaction (H{sub 2}O + SO{sub 3}{sup 2-} {yields} H{sub 2} + SO{sub 4}{sup 2-}, {delta}G = -17.68 kJ mol{sup -1}). The best activity occurs over Fe{sub 1.2}Cr{sub 0.8}O{sub 3} in SO{sub 3}{sup 2-} (0.1 M) solution with H{sub 2} liberation rate of 21.7 {mu}mol g{sup -1} min{sup -1} and a quantum yield 0.06% under polychromatic light. Over time, a pronounced deceleration occurs, due to the competitive reduction of the end product S{sub 2}O{sub 6}{sup 2-}. (author)

  3. Experimental and Numerical Evaluation of the By-Pass Flow in a Catalytic Plate Reactor for Hydrogen Production

    DEFF Research Database (Denmark)

    Sigurdsson, Haftor Örn; Kær, Søren Knudsen

    2011-01-01

    Numerical and experimental study is performed to evaluate the reactant by-pass flow in a catalytic plate reactor with a coated wire mesh catalyst for steam reforming of methane for hydrogen generation. By-pass of unconverted methane is evaluated under different wire mesh catalyst width to reactor...

  4. Progress in Catalytic Membrane Reactors for High Purity Hydrogen Production%膜催化反应器及其制氢技术的研究进展

    Institute of Scientific and Technical Information of China (English)

    闫云飞; 张力; 李丽仙; 唐强

    2011-01-01

    As a kind of ideal fuel for fuel cell, hydrogen must be satisfied with the enough high purity. To produce high purity hydrogen at a low cost and large scale method has become a key research focus in the industrialization of fuel-cell technology. The membrane catalytic technology with catalysis and separation dual functions has been developed in recent years, which is a good method to produce high purity hydrogen. Based on the latest developments in the membrane catalytic reaction fields, the advantages, composition and type of membrane catalytic reactor are summarized. The preparation techniques, advantages and classification of inorganic membrane materials are described. Especially, the progress and application for high purity hydrogen production are reviewed in three kinds of catalytic membrane reactors, including oxygen-permeable membrane reactor, hydrogen-permeation membrane reactor and double-membranes reactor. The existing problems of catalytic membrane and membrane catalytic reactor in the industrialization process of hydrogen production using the membrane catalytic technology are also discussed. Additionally, the prospects of membrane catalytic reactors for hydrogen production is proposed.%燃料电池对其理想燃料氢气的纯度要求极高,如何低成本、大规模制取高纯氢气己成为燃料电池技术实现工业化的一个关键问题和研究热点.近年发展起来的兼具催化与分离双重功能的膜催化反应技术是实现制取高纯氢气的一个有效途径.本文结合膜催化反应领域的最新进展,综述了膜催化反应器的优点、组成、类型;介绍了无机膜材料的优点、分类及制备技术;详细综述了透氧膜催化反应器、透氢膜催化反应器及双膜催化反应器在制氢过程中的研究进展和应用,指出了膜催化反应制氢技术在工业化发展过程中存在的问题及应用前景.

  5. Chemistry - Toward efficient hydrogen production at surfaces

    DEFF Research Database (Denmark)

    Nørskov, Jens Kehlet; Christensen, Claus H.

    2006-01-01

    Calculations are providing a molecular picture of hydrogen production on catalytic surfaces and within enzymes, knowledge that may guide the design of new, more efficient catalysts for the hydrogen economy.......Calculations are providing a molecular picture of hydrogen production on catalytic surfaces and within enzymes, knowledge that may guide the design of new, more efficient catalysts for the hydrogen economy....

  6. Thermo catalytic decomposition of methane over Pd/AC and Pd/CB catalysts for hydrogen production and carbon nanofibers formation

    Directory of Open Access Journals (Sweden)

    K. Srilatha

    2014-09-01

    Full Text Available Hydrogen production studies have been carried using Thermo Catalytic Decomposition (TCD Unit. Thermo catalytic decomposition of methane is an attractive route for COx free production of hydrogen required in fuel cells. Although metal based catalysts produce hydrogen at low temperatures, carbon formed during methane decomposition reaction rapidly deactivates the catalyst. The present work compares the results of 10 wt% Pd supported on commercially available activated carbon and carbon black catalysts (samples coded as Pd10/AC and Pd10/CB respectively for methane decomposition reaction. Hydrogen has been produced by thermo catalytic decomposition of methane at 1123K and Volume Hourly Space Velocity (VHSV of 1.62 L/h g on the activity of both the catalysts has been studied. XRD of the above catalysts revealed, moderately crystalline peaks of Pd which may be responsible for the increase in catalytic life and formation of carbon fibers. Also during life studies (850°C and 54 sccm of methane it has been observed that the activity of carbon black is sustainable for a longer time compared to that of activated carbon.

  7. Green diesel production via catalytic hydrogenation/decarboxylation of triglycerides and fatty acids of vegetable oil and brown grease

    Science.gov (United States)

    Sari, Elvan

    than activated carbon itself for both decarboxylation of oleic acid and hydrogenation of alkenes. In an additional effort to reduce Pd amount in the catalyst, Pd2Co/C catalysts with various Pd content were prepared and the catalytic activity study showed that 0.5 wt% Pd2Co/C catalyst performs even better than a 5 wt% Pd/C catalyst. Pd and Co alloys were very well dispersed and formed fine clusters, which led to a higher active metal surface area and hence favored the decarboxylation of oleic acid. This study showed that an alloy of Pd on carbon with a significantly low Pd content is much more active and selective to diesel hydrocarbons production from an unsaturated fatty acid in super-critical water and may be regarded as a prospective feasible decarboxylation catalyst for the removal of oxygen from vegetable oil/animal fat without the need of additional hydrogen.

  8. Molecular hydrogen and catalytic combustion in the production of hyperpolarized 83Kr and 129Xe MRI contrast agents

    Science.gov (United States)

    Rogers, Nicola J.; Hill-Casey, Fraser; Stupic, Karl F.; Six, Joseph S.; Lesbats, Clémentine; Rigby, Sean P.; Fraissard, Jacques; Pavlovskaya, Galina E.; Meersmann, Thomas

    2016-03-01

    Hyperpolarized (hp) 83Kr is a promising MRI contrast agent for the diagnosis of pulmonary diseases affecting the surface of the respiratory zone. However, the distinct physical properties of 83Kr that enable unique MRI contrast also complicate the production of hp 83Kr. This work presents a previously unexplored approach in the generation of hp 83Kr that can likewise be used for the production of hp 129Xe. Molecular nitrogen, typically used as buffer gas in spin-exchange optical pumping (SEOP), was replaced by molecular hydrogen without penalty for the achievable hyperpolarization. In this particular study, the highest obtained nuclear spin polarizations were P = 29% for 83Kr and P = 63% for 129Xe. The results were reproduced over many SEOP cycles despite the laser-induced on-resonance formation of rubidium hydride (RbH). Following SEOP, the H2 was reactively removed via catalytic combustion without measurable losses in hyperpolarized spin state of either 83Kr or 129Xe. Highly spin-polarized 83Kr can now be purified for the first time, to our knowledge, to provide high signal intensity for the advancement of in vivo hp 83Kr MRI. More generally, a chemical reaction appears as a viable alternative to the cryogenic separation process, the primary purification method of hp 129Xe for the past 2 1/2 decades. The inherent simplicity of the combustion process will facilitate hp 129Xe production and should allow for on-demand continuous flow of purified and highly spin-polarized 129Xe.

  9. Hydrogen production by steam reforming of bio-alcohols. The use of conventional and membrane-assisted catalytic reactors

    Energy Technology Data Exchange (ETDEWEB)

    Seelam, P. K.

    2013-11-01

    The energy consumption around the globe is on the rise due to the exponential population growth and urbanization. There is a need for alternative and non-conventional energy sources, which are CO{sub 2}-neutral, and a need to produce less or no environmental pollutants and to have high energy efficiency. One of the alternative approaches is hydrogen economy with the fuel cell (FC) technology which is forecasted to lead to a sustainable society. Hydrogen (H{sub 2}) is recognized as a potential fuel and clean energy carrier being at the same time a carbon-free element. Moreover, H{sub 2} is utilized in many processes in chemical, food, metallurgical, and pharmaceutical industry and it is also a valuable chemical in many reactions (e.g. refineries). Non-renewable resources have been the major feedstock for H{sub 2} production for many years. At present, {approx}50% of H{sub 2} is produced via catalytic steam reforming of natural gas followed by various down-stream purification steps to produce {approx}99.99% H{sub 2}, the process being highly energy intensive. Henceforth, bio-fuels like biomass derived alcohols (e.g. bio-ethanol and bio-glycerol), can be viable raw materials for the H{sub 2} production. In a membrane based reactor, the reaction and selective separation of H{sub 2} occur simultaneously in one unit, thus improving the overall reactor efficiency. The main motivation of this work is to produce H{sub 2} more efficiently and in an environmentally friendly way from bio-alcohols with a high H{sub 2} selectivity, purity and yield. In this thesis, the work was divided into two research areas, the first being the catalytic studies using metal decorated carbon nanotube (CNT) based catalysts in steam reforming of ethanol (SRE) at low temperatures (<450 deg C). The second part was the study of steam reforming (SR) and the water-gas-shift (WGS) reactions in a membrane reactor (MR) using dense and composite Pd-based membranes to produce high purity H{sub 2}. CNTs

  10. Hydrogen production from catalytic decomposition of methane; Produccion de hidrogeno a partir de la descomposicion termica catalitica del biogas de digestion anaerobia

    Energy Technology Data Exchange (ETDEWEB)

    Belsue Echevarria, M.; Etxebeste Juarez, O.; Perez Gil, S.

    2002-07-01

    The need of substitution of part of the energy obtained from fossil fuels instead of energy from renewable sources, together with the minimal emissions of CO{sub ''} and CO that are expected with these technologies, make renewable sources a very attractive predecessor for the production of hydrogen. In this situation, a usable source for hydrogen production is the biogas achieved by means of technologies like the anaerobic digestion of different kinds of biomass (MSW, sewage sludge, stc.). In this article we suggest the Thermal Catalytic Decomposition of the methane contained in this biogas, after separation of pollutants like CO{sub ''}, H{sub 2}S. steam. This technology will give hydrogen, usable in fuel cells, and nanoestructured carbon as products. (Author) 7 refs.

  11. Photoelectrochemical hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Rocheleau, R.E.; Miller, E.; Misra, A. [Univ. of Hawaii, Honolulu, HI (United States)

    1996-10-01

    The large-scale production of hydrogen utilizing energy provided by a renewable source to split water is one of the most ambitious long-term goals of the U.S. Department of Energy`s Hydrogen Program. One promising option to meet this goal is direct photoelectrolysis in which light absorbed by semiconductor-based photoelectrodes produces electrical power internally to split water into hydrogen and oxygen. Under this program, direct solar-to-chemical conversion efficiencies as high as 7.8 % have been demonstrated using low-cost, amorphous-silicon-based photoelectrodes. Detailed loss analysis models indicate that solar-to-chemical conversion greater than 10% can be achieved with amorphous-silicon-based structures optimized for hydrogen production. In this report, the authors describe the continuing progress in the development of thin-film catalytic/protective coatings, results of outdoor testing, and efforts to develop high efficiency, stable prototype systems.

  12. Advanced Catalytic Hydrogenation Retrofit Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Reinaldo M. Machado

    2002-08-15

    Industrial hydrogenation is often performed using a slurry catalyst in large stirred-tank reactors. These systems are inherently problematic in a number of areas, including industrial hygiene, process safety, environmental contamination, waste production, process operability and productivity. This program proposed the development of a practical replacement for the slurry catalysts using a novel fixed-bed monolith catalyst reactor, which could be retrofitted onto an existing stirred-tank reactor and would mitigate many of the minitations and problems associated with slurry catalysts. The full retrofit monolith system, consisting of a recirculation pump, gas/liquid ejector and monolith catalyst, is described as a monolith loop reactor or MLR. The MLR technology can reduce waste and increase raw material efficiency, which reduces the overall energy required to produce specialty and fine chemicals.

  13. Performance characterization of a hydrogen catalytic heater.

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Terry Alan; Kanouff, Michael P.

    2010-04-01

    This report describes the performance of a high efficiency, compact heater that uses the catalytic oxidation of hydrogen to provide heat to the GM Hydrogen Storage Demonstration System. The heater was designed to transfer up to 30 kW of heat from the catalytic reaction to a circulating heat transfer fluid. The fluid then transfers the heat to one or more of the four hydrogen storage modules that make up the Demonstration System to drive off the chemically bound hydrogen. The heater consists of three main parts: (1) the reactor, (2) the gas heat recuperator, and (3) oil and gas flow distribution manifolds. The reactor and recuperator are integrated, compact, finned-plate heat exchangers to maximize heat transfer efficiency and minimize mass and volume. Detailed, three-dimensional, multi-physics computational models were used to design and optimize the system. At full power the heater was able to catalytically combust a 10% hydrogen/air mixture flowing at over 80 cubic feet per minute and transfer 30 kW of heat to a 30 gallon per minute flow of oil over a temperature range from 100 C to 220 C. The total efficiency of the catalytic heater, defined as the heat transferred to the oil divided by the inlet hydrogen chemical energy, was characterized and methods for improvement were investigated.

  14. A comparative parametric study of a catalytic plate methane reformer coated with segmented and continuous layers of combustion catalyst for hydrogen production

    Science.gov (United States)

    Mundhwa, Mayur; Parmar, Rajesh D.; Thurgood, Christopher P.

    2017-03-01

    A parametric comparison study is carried out between segmented and conventional continuous layer configurations of the coated combustion-catalyst to investigate their influence on the performance of methane steam reforming (MSR) for hydrogen production in a catalytic plate reactor (CPR). MSR is simulated on one side of a thin plate over a continuous layer of nickel-alumina catalyst by implementing an experimentally validated surface microkinetic model. Required thermal energy for the MSR reaction is supplied by simulating catalytic methane combustion (CMC) on the opposite side of the plate over segmented and continuous layer of a platinum-alumina catalyst by implementing power law rate model. The simulation results of both coating configurations of the combustion-catalyst are compared using the following parameters: (1) co-flow and counter-flow modes between CMC and MSR, (2) gas hourly space velocity and (3) reforming-catalyst thickness. The study explains why CPR designed with the segmented combustion-catalyst and co-flow mode shows superior performance not only in terms of high hydrogen production but also in terms of minimizing the maximum reactor plate temperature and thermal hot-spots. The study shows that the segmented coating requires 7% to 8% less combustion-side feed flow and 70% less combustion-catalyst to produce the required flow of hydrogen (29.80 mol/h) on the reforming-side to feed a 1 kW fuel-cell compared to the conventional continuous coating of the combustion-catalyst.

  15. Autothermal catalytic pyrolysis of methane as a new route to hydrogen production with reduced CO{sub 2} emissions

    Energy Technology Data Exchange (ETDEWEB)

    Muradov, Nazim; Smith, Franklyn; Huang, Cunping; T-Raissi, Ali [Florida Solar Energy Center, University of Central Florida, Cocoa, FL 32922 (United States)

    2006-08-15

    Hydrogen production plants are among major sources of CO{sub 2} emissions into the atmosphere. The objective of this paper is to explore new routes to hydrogen production from natural gas (or methane) with drastically reduced CO{sub 2} emissions. One approach analyzed in this paper is based on thermocatalytic decomposition (or pyrolysis) of methane into hydrogen gas and elemental carbon over carbon-based catalysts. Several heat input options to the endothermic process are discussed in the paper. The authors conduct thermodynamic analysis of methane decomposition in the presence of small amounts of oxygen in an autothermal (or thermo-neutral) regime using AspenPlus(TM) chemical process simulator. Methane conversion, products yield, effluent gas composition, process enthalpy flows as a function of temperature, pressure and O{sub 2}/CH{sub 4} ratio has been determined. CO{sub 2} emissions (per m{sup 3} of H{sub 2} produced) from the process could potentially be a factor of 3-5 less than from conventional hydrogen production processes. Oxygen-assisted decomposition of methane over activated carbon (AC) and AC-supported iron catalysts over wide range of temperatures and O{sub 2}/CH{sub 4} ratios was experimentally verified. Problems associated with the catalyst deactivation and the effect of iron doping on the catalyst stability are discussed. (author)

  16. Characterization of Ni and W co-loaded SBA-15 catalyst and its hydrogen production catalytic ability on ethanol steam reforming reaction

    Science.gov (United States)

    Kim, Dongjin; Kwak, Byeong Sub; Min, Bong-Ki; Kang, Misook

    2015-03-01

    This study evaluated the application of advanced bimetallic catalytic species of Ni and W to effectively produce hydrogen gases from ethanol steam reforming. The highest reactivity was achieved using the Ni0.95W0.05/SBA-15 catalyst. The maximum H2 production and ethanol conversion of 90% and 85%, respectively, were obtained for 0.4 g catalyst at 600 °C after 10 h with a EtOH:H2O ratio of 1:3 and a gas hourly space velocity of 6000 h-1. This highlights a synergy between the Ni and W loading on SBA-15 during ethanol steam reforming that occurs through the inhibition of Ni particle agglomeration and consequent decrease in catalytic deactivation. Additionally, the supplied W ingredients promoted CO2 selectivity, which was generated from the CO-water gas shift reaction.

  17. Catalytic hydrothermal gasification of algae for hydrogen production: composition of reaction products and potential for nutrient recycling.

    Science.gov (United States)

    Onwudili, Jude A; Lea-Langton, Amanda R; Ross, Andrew B; Williams, Paul T

    2013-01-01

    Chlorella vulgaris, Spirulina platensis and Saccharina latissima were processed under supercritical water gasification conditions at 500 °C, 36 MPa in an Inconel batch reactor for 30 min in the presence/absence of NaOH and/or Ni-Al(2)O(3). Hydrogen gas yields were more than two times higher in the presence of NaOH than in its absence and tar yields were reduced by up to 71%. Saccharina, a carbohydrate-rich macro-alga, gave the highest hydrogen gas yields of 15.1 mol/kg. The tars from all three algae contained aromatic compounds, including phenols, alkyl benzenes and polycyclic aromatic hydrocarbons as well as heterocyclic nitrogen compounds. Tars from Chlorella and Spirulina contained high yields of pyridines, pyrroles, indoles and pyrimidines. Up to 97% TOC removal were achieved in the process waters from the gasification of the algae. Analyses for specific nutrients in the process waters indicated that the process waters from Saccharina could potentially be used for microalgae cultivation.

  18. On the role of metal particle size and surface coverage for photo-catalytic hydrogen production; a case study of the Au/CdS system

    KAUST Repository

    Majeed, I.

    2015-09-25

    Photo-catalytic hydrogen production has been studied on Au supported CdS catalysts under visible light irradiation in order to understand the effect of Au particle size as well as the reaction medium properties. Au nanoparticles of size about 2-5 nm were deposited over hexagonal CdS particles using a new simple method involving reduction of Au3+ ions with iodide ions. Within the investigated range of Au (between 1 and 5 wt. %) fresh particles with mean size of 4 nm and XPS Au4f/Cd3d surface ratio of 0.07 showed the highest performance (ca. 1 molecule of H2 / Auatom s−1) under visible light irradiation (>420 nm and a flux of 35 mW/cm2). The highest hydrogen production rate was obtained from water (92%)-ethanol (8%) in an electrolyte medium (Na2S-Na2SO3). TEM studies of fresh and used catalysts showed that Au particle size increases (almost 5 fold) with increasing photo-irradiation time due to photo-agglomeration effect yet no sign of deactivation was observed. A mechanism for hydrogen production from ethanol-water electrolyte mixture is presented and discussed.

  19. Valorization of Waste Lipids through Hydrothermal Catalytic Conversion to Liquid Hydrocarbon Fuels with in Situ Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Dongwook; Vardon, Derek R.; Murali, Dheeptha; Sharma, Brajendra K.; Strathmann, Timothy J.

    2016-03-07

    We demonstrate hydrothermal (300 degrees C, 10 MPa) catalytic conversion of real waste lipids (e.g., waste vegetable oil, sewer trap grease) to liquid hydrocarbon fuels without net need for external chemical inputs (e.g., H2 gas, methanol). A supported bimetallic catalyst (Pt-Re/C; 5 wt % of each metal) previously shown to catalyze both aqueous phase reforming of glycerol (a triacylglyceride lipid hydrolysis coproduct) to H2 gas and conversion of oleic and stearic acid, model unsaturated and saturated fatty acids, to linear alkanes was applied to process real waste lipid feedstocks in water. For reactions conducted with an initially inert headspace gas (N2), waste vegetable oil (WVO) was fully converted into linear hydrocarbons (C15-C17) and other hydrolyzed byproducts within 4.5 h, and H2 gas production was observed. Addition of H2 to the initial reactor headspace accelerated conversion, but net H2 production was still observed, in agreement with results obtained for aqueous mixtures containing model fatty acids and glycerol. Conversion to liquid hydrocarbons with net H2 production was also observed for a range of other waste lipid feedstocks (animal fat residuals, sewer trap grease, dry distiller's grain oil, coffee oil residual). These findings demonstrate potential for valorization of waste lipids through conversion to hydrocarbons that are more compatible with current petroleum-based liquid fuels than the biodiesel and biogas products of conventional waste lipid processing technologies.

  20. Ultrathin Co(Ni)-doped MoS2 nanosheets as catalytic promoters enabling efficient solar hydrogen production

    Institute of Scientific and Technical Information of China (English)

    Xiaoyan Ma; Jinquan Li; Changhua An; Juan Feng; Yuhua Chi; Junxue Liu; Jun Zhang

    2016-01-01

    The design of efficient artificial photosynthetic systems that harvest solar energy to drive the hydrogen evolution reaction via water reduction is of great importance from both the theoretical and practical viewpoints.Integrating appropriate co-catalyst promoters with strong light absorbing materials represents an ideal strategy to enhance the conversion efficiency of solar energy in hydrogen production.Herein,we report,for the first time,the synthesis of a class of unique hybrid structures consisting of ultrathin Co(Ni)-doped MoS2 nanosheets (co-catalyst promoter) intimately grown on semiconductor CdS nanorods (light absorber).The as-synthesized one-dimensional CdS@doped-MoS2 heterostructures exhibited very high photocatalytic activity (with a quantum yield of 17.3%) and stability towards H2 evolution from the photoreduction of water.Theoretical calculations revealed that Ni doping can increase the number of uncoordinated atoms at the edge sites of MoS2 nanosheets to promote electron transfer across the CdS/MoS2 interfaces as well as hydrogen reduction,leading to an efficient H2 evolution reaction.

  1. Energy efficient production of hydrogen and syngas from biomass: development of low-temperature catalytic process for cellulose gasification.

    Science.gov (United States)

    Asadullah, Mohammad; Ito, Shin-ichi; Kunimori, Kimio; Yamada, Muneyoshi; Tomishige, Keiichi

    2002-10-15

    The Rh/CeO2/M (M = SiO2, Al2O3, and ZrO2) type catalysts with various compositions have been prepared and investigated in the gasification of cellulose, a model compound of biomass, in a fluidized bed reactor at 500-700 degrees C. The conventional nickel and dolomite catalysts have also been investigated. Among the catalysts, Rh/CeO2/SiO2 with 35% CeO2 has been found to be the best catalyst with respect to the carbon conversion to gas and product distribution. The steam addition contributed to the complete conversion of cellulose to gas even at 600 degrees C. Lower steam supply gave the syngas and higher steam supply gave the hydrogen as the major product. Hydrogen and syngas from cellulose or cellulosic biomass gasification are environmentally super clean gaseous fuels for power generation. Moreover, the syngas derived liquid fuels such as methanol, dimethyl ether, and synthetic diesels are also super clean transportation fuels. However, the use of cellulose or cellulosic biomass for energy source through the gasification is challenging because of the formation of tar and char during the gasification process. It is interesting that no tar or char was finally formed in the effluent gas at as low as 500-600 degrees C using Rh/CeO2/SiO2(35) catalyst in this process.

  2. Hydrogen production via catalytic steam reforming of fast pyrolysis bio-oil in a two-stage fixed bed reactor system

    Energy Technology Data Exchange (ETDEWEB)

    Wu, C.; Huang, Q.; Sui, M.; Yan, Y.; Wang, F. [Research Center for Biomass Energy, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237 (China)

    2008-12-15

    Hydrogen production was prepared via catalytic steam reforming of fast pyrolysis bio-oil in a two-stage fixed bed reactor system. Low-cost catalyst dolomite was chosen for the primary steam reforming of bio-oil in consideration of the unavoidable deactivation caused by direct contact of metal catalyst and bio-oil itself. Nickel-based catalyst Ni/MgO was used in the second stage to increase the purity and the yield of desirable gas product further. Influential parameters such as temperature, steam to carbon ratio (S/C, S/CH{sub 4}), and material space velocity (W{sub B}HSV, GHSV) both for the first and the second reaction stages on gas product yield, carbon selectivity of gas product, CH{sub 4} conversion as well as purity of desirable gas product were investigated. High temperature (> 850 C) and high S/C (> 12) are necessary for efficient conversion of bio-oil to desirable gas product in the first steam reforming stage. Low W{sub B}HSV favors the increase of any gas product yield at any selected temperature and the overall conversion of bio-oil to gas product increases accordingly. Nickel-based catalyst Ni/MgO is effective in purification stage and 100% conversion of CH{sub 4} can be obtained under the conditions of S/CH{sub 4} no less than 2 and temperature no less than 800 C. Low GHSV favors the CH{sub 4} conversion and the maximum CH{sub 4} conversion 100%, desirable gas product purity 100%, and potential hydrogen yield 81.1% can be obtained at 800 C provided that GHSV is no more than 3600 h{sup -} {sup 1}. Carbon deposition behaviors in one-stage reactor prove that the steam reforming of crude bio-oil in a two-stage fixed bed reaction system is necessary and significant. (author)

  3. Catalytic production of biodiesel

    Energy Technology Data Exchange (ETDEWEB)

    Theilgaard Madsen, A.

    2011-07-01

    The focus of this thesis is the catalytic production of diesel from biomass, especially emphasising catalytic conversion of waste vegetable oils and fats. In chapter 1 an introduction to biofuels and a review on different catalytic methods for diesel production from biomass is given. Two of these methods have been used industrially for a number of years already, namely the transesterification (and esterification) of oils and fats with methanol to form fatty acid methyl esters (FAME), and the hydrodeoxygenation (HDO) of fats and oils to form straight-chain alkanes. Other possible routes to diesel include upgrading and deoxygenation of pyrolysis oils or aqueous sludge wastes, condensations and reductions of sugars in aqueous phase (aqueous-phase reforming, APR) for monofunctional hydrocarbons, and gasification of any type of biomass followed by Fischer-Tropsch-synthesis for alkane biofuels. These methods have not yet been industrialised, but may be more promising due to the larger abundance of their potential feedstocks, especially waste feedstocks. Chapter 2 deals with formation of FAME from waste fats and oils. A range of acidic catalysts were tested in a model fat mixture of methanol, lauric acid and trioctanoin. Sulphonic acid-functionalised ionic liquids showed extremely fast convertion of lauric acid to methyl laurate, and trioctanoate was converted to methyl octanoate within 24 h. A catalyst based on a sulphonated carbon-matrix made by pyrolysing (or carbonising) carbohydrates, so-called sulphonated pyrolysed sucrose (SPS), was optimised further. No systematic dependency on pyrolysis and sulphonation conditions could be obtained, however, with respect to esterification activity, but high activity was obtained in the model fat mixture. SPS impregnated on opel-cell Al{sub 2}O{sub 3} and microporous SiO{sub 2} (ISPS) was much less active in the esterification than the original SPS powder due to low loading and thereby low number of strongly acidic sites on the

  4. Simulation Studies of the Hydrogen Production from Methanol Partial Oxidation Steam Reforming by a Tubular Packed-bed Catalytic Reactor

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Hydrogen production by partial oxidation steam reforming of methanol over a Cu/ZnO/Al2 O3 cata lyst has been paid more and more attention. The chemical equilibria involved in the methanol partial oxidation steam reforming reaction network such as methanol partial oxidation, methanol steam reforming, decomposition of methanol and water-gas shift reaction have been examined over the ranges of temperature 473-1073 K under normal pressure. Based on the detailed kinetics of these reactions over a Cu/ZnO/Al2O3 catalyst, and from the basic concept of the effectiveness factor, the intraparticle diffusion limitations were taken into account. The effec tiveness factors for each reaction along the bed length were calculated. Then important results were offered for the simulation of this reaction process.

  5. Simulation Studies of the Hydrogen Production from Methanol Partial Oxidation Steam Reforming by a Tubular Packed-bed Catalytic Reactor*

    Institute of Scientific and Technical Information of China (English)

    蒋元力; 林美淑; 金东显

    2001-01-01

    Hydrogen production by partial oxidation steam reforming of methanol over a Cu/ZnO/Al2O3 cata-lyst has been paid more and more attention. The chemical equilibria involved in the methanol pvxtial oxidation steam reforming reaction network such as methanol partial oxidation, methanol steam reforming, decomposition of methanol and water-gas shift reaction have been examined over the ranges of temperature 473---1073 K under normal pressure. Based on the detailed kinetics of these reactions over a Cu/ZnO/Al2O3 catalyst, and from the basic concept of the effectiveness factor, the intraparticle diffusion limitations were taken into account. The effectiveness factors for each reaction along the bed length were calculated. Then important results were offered for the simulation of this reaction process.

  6. Photoelectrochemical hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Rocheleau, R.E.; Miller, E.; Zhang, Z. [Univ. of Hawaii, Honolulu, HI (United States)

    1995-09-01

    The large-scale production of hydrogen utilizing energy provided by a renewable source to split water is one of the most ambitious long-term goals of the U.S. Department of Energy`s Hydrogen Program. Photoelectrochemical devices-direct photoconversion systems utilizing a photovoltaic-type structure coated with water-splitting catalysts-represent a promising option to meet this goal. Direct solar-to-chemical conversion efficiencies greater than 7% and photoelectrode lifetimes of up to 30 hours in 1 molar KOH have been demonstrated in our laboratory using low-cost, amorphous-silicon-based photoelectrodes. Loss analysis models indicate that the DOE`s goal of 10% solar-to-chemical conversion can be met with amorphous-silicon-based structures optimized for hydrogen production. In this report, we describe recent progress in the development of thin-film catalytic/protective coatings, improvements in photoelectrode efficiency and stability, and designs for higher efficiency and greater stability.

  7. Production of bio-hydrogenated diesel by catalytic hydrotreating of palm oil over NiMoS2/γ-Al2O3 catalyst.

    Science.gov (United States)

    Srifa, Atthapon; Faungnawakij, Kajornsak; Itthibenchapong, Vorranutch; Viriya-Empikul, Nawin; Charinpanitkul, Tawatchai; Assabumrungrat, Suttichai

    2014-04-01

    Catalytic hydrotreating of palm oil (refined palm olein type) to produce bio-hydrogenated diesel (BHD) was carried out in a continuous-flow fixed-bed reactor over NiMoS2/γ-Al2O3 catalyst. Effects of dominant hydrotreating parameters: temperature: 270-420°C; H2 pressure: 15-80 bar; LHSV: 0.25-5.0 h(-1); and H2/oil ratio: 250-2000 N(cm(3)/cm(3)) on the conversion, product yield, and a contribution of hydrodeoxygenation (HDO) and decarbonylation/decarboxylation (DCO/DCO2) were investigated to find the optimal hydrotreating conditions. All calculations including product yield and the contribution of HDO and DCO/DCO2 were extremely estimated based on mole balance corresponding to the fatty acid composition in feed to fully understand deoxygenation behaviors at different conditions. These analyses demonstrated that HDO, DCO, and DCO2 reactions competitively occurred at each condition, and had different optimal and limiting conditions. The differences in the hydrotreating reactions, liquid product compositions, and gas product composition were also discussed.

  8. Catalytic Hydrogenation of Acetone to Isopropanol: An Environmentally Benign Approach

    Directory of Open Access Journals (Sweden)

    Ateeq Rahman

    2011-01-01

    Full Text Available The catalytic hydrogenation of acetone is an important area of catalytic process to produce fine chemicals. Hydrogenation of acetone has important applications for heat pumps, fuel cells or in fulfilling the sizeable demand for the production of 2-propanol. Catalytic vapour phase hydrogenation of acetone has gained attention over the decades with variety of homogeneous catalysts notably Iridium, Rh, Ru complexes and heterogeneous catalysts comprising of Raney Nickel, Raney Sponge, Ni/Al2O3, Ni/SiO2, or Co-Al2O3, Pd, Rh, Ru, Re, or Fe/Al2O3 supported on SiO2 or MgO and even CoMgAl, NiMg Al layered double hydroxide, Cu metal, CuO, Cu2O. Nano catalysts are developed for actone reduction Ni maleate, cobalt oxide prepared in organic solvents. Author present a review on acetone hydrogenation under different conditions with various homogeneous and heterogeneous catalysts studied so far in literature and new strategies to develop economic and environmentally benign approach. ©2010 BCREC UNDIP. All rights reserved(Received: 16th June 2010, Revised: 18th October 2010; Accepted: 25th October 2010[How to Cite:Ateeq Rahman. (2010. Catalytic Hydrogenation of Acetone to Isopropanol: An Environmentally Benign Approach. Bulletin of Chemical Reaction Engineering and Catalysis, 5(2: 113-126. doi:10.9767/bcrec.5.2.798.113-126][DOI: http://dx.doi.org/10.9767/bcrec.5.2.798.113-126 || or local:  http://ejournal.undip.ac.id/index.php/bcrec/article/view/798

  9. Solar hydrogen production: renewable hydrogen production by dry fuel reforming

    Science.gov (United States)

    Bakos, Jamie; Miyamoto, Henry K.

    2006-09-01

    SHEC LABS - Solar Hydrogen Energy Corporation constructed a pilot-plant to demonstrate a Dry Fuel Reforming (DFR) system that is heated primarily by sunlight focusing-mirrors. The pilot-plant consists of: 1) a solar mirror array and solar concentrator and shutter system; and 2) two thermo-catalytic reactors to convert Methane, Carbon Dioxide, and Water into Hydrogen. Results from the pilot study show that solar Hydrogen generation is feasible and cost-competitive with traditional Hydrogen production. More than 95% of Hydrogen commercially produced today is by the Steam Methane Reformation (SMR) of natural gas, a process that liberates Carbon Dioxide to the atmosphere. The SMR process provides a net energy loss of 30 to 35% when converting from Methane to Hydrogen. Solar Hydrogen production provides a 14% net energy gain when converting Methane into Hydrogen since the energy used to drive the process is from the sun. The environmental benefits of generating Hydrogen using renewable energy include significant greenhouse gas and criteria air contaminant reductions.

  10. Hydrogen production with short contact time. Catalytic partial oxidation of hydrocarbons and oxygenated compounds: Recent advances in pilot- and bench-scale testing and process design

    Energy Technology Data Exchange (ETDEWEB)

    Guarinoni, A.; Ponzo, R.; Basini, L. [ENI Refining and Marketing Div., San Donato Milanese (Italy)

    2010-12-30

    ENI R and D has been active for fifteen years in the development of Short Contact Time - Catalytic Partial Oxidation (SCT-CPO) technologies for producing Hydrogen/Synthesis Gas. From the beginning the experimental work addressed either at defining the fundamental principles or the technical and economical potential of the technology. Good experimental responses, technical solutions' simplicity and flexibility, favourable techno-economical evaluations promoted the progressive widening of the field of the investigations. From Natural Gas (NG) the range of ''processable'' Hydrocarbons extended to Liquefied Petroleum Gas (LPG) and Gasoils, including those characterised by high levels of unsaturated and sulphurated molecules and, lately, to other compounds with biological origin. The extensive work led to the definition of different technological solutions, grouped as follows: Technology 1: Air Blown SCT-CPO of Gaseous Hydrocarbons and/or Light Compounds with biological origin Technology 2: Enriched Air/Oxygen Blown SCT-CPO of Gaseous Hydrocarbons and/or Light Compounds with biological origin Technology 3: Enriched Air/Oxygen Blown SCT-CPO of Liquid Hydrocarbons and/or Compounds with biological origin Recently, the licence rights on a non-exclusive basis for the commercialisation of SCT-CPO based processes for H{sub 2}/Synthesis gas production from light hydrocarbons with production capacity lower than 5,000 Nm{sup 3}/h of H{sub 2} or 7,500 Nm3/h of syngas have been assigned to two external companies. In parallel, development of medium- and large-scale plant solutions is progressing within the ENI group framework. These last activities are addressed to the utilisation of SCT-CPO for matching the variable Hydrogen demand in several contexts of oil refining operation. This paper will report on the current status of SCT-CPO with a focus on experimental results obtained, either at pilot- and bench- scale level. (orig.)

  11. Hydrogen production by Cyanobacteria

    Directory of Open Access Journals (Sweden)

    Chaudhuri Surabhi

    2005-12-01

    Full Text Available Abstract The limited fossil fuel prompts the prospecting of various unconventional energy sources to take over the traditional fossil fuel energy source. In this respect the use of hydrogen gas is an attractive alternate source. Attributed by its numerous advantages including those of environmentally clean, efficiency and renew ability, hydrogen gas is considered to be one of the most desired alternate. Cyanobacteria are highly promising microorganism for hydrogen production. In comparison to the traditional ways of hydrogen production (chemical, photoelectrical, Cyanobacterial hydrogen production is commercially viable. This review highlights the basic biology of cynobacterial hydrogen production, strains involved, large-scale hydrogen production and its future prospects. While integrating the existing knowledge and technology, much future improvement and progress is to be done before hydrogen is accepted as a commercial primary energy source.

  12. Photobiological hydrogen production.

    Science.gov (United States)

    Asada, Y; Miyake, J

    1999-01-01

    The principles and recent progress in the research and development of photobiological hydrogen production are reviewed. Cyanobacteria produce hydrogen gas using nitrogenase and/or hydrogenase. Hydrogen production mediated by native hydrogenases in cyanobacteria occurs under in the dark under anaerobic conditions by degradation of intracellular glycogen. In vitro and in vivo coupling of the cyanobacterial photosynthetic system with a clostridial hydrogenase via cyanobacterial ferredoxin was demonstrated in the presence of light. Genetic transformation of Synechococcus PCC7942 with the hydrogenase gene from Clostridium pasteurianum was successful; the active enzyme was expressed in PCC7942. The strong hydrogen producers among photosynthetic bacteria were isolated and characterized. Coculture of Rhodobacter and Clostriudium was applied for hydrogen production from glucose. A mutant strain of Rhodobacter sphaeroides RV whose light-harvesting proteins were altered was obtained by UV irradiation. Hydrogen productivity by the mutant was improved when irradiated with monochromatic light of some wavelengths. The development of photobioreactors for hydrogen production is also reviewed.

  13. Microchannel Reactor System for Catalytic Hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Adeniyi Lawal; Woo Lee; Ron Besser; Donald Kientzler; Luke Achenie

    2010-12-22

    We successfully demonstrated a novel process intensification concept enabled by the development of microchannel reactors, for energy efficient catalytic hydrogenation reactions at moderate temperature, and pressure, and low solvent levels. We designed, fabricated, evaluated, and optimized a laboratory-scale microchannel reactor system for hydrogenation of onitroanisole and a proprietary BMS molecule. In the second phase of the program, as a prelude to full-scale commercialization, we designed and developed a fully-automated skid-mounted multichannel microreactor pilot plant system for multiphase reactions. The system is capable of processing 1 – 10 kg/h of liquid substrate, and an industrially relevant immiscible liquid-liquid was successfully demonstrated on the system. Our microreactor-based pilot plant is one-of-akind. We anticipate that this process intensification concept, if successfully demonstrated, will provide a paradigm-changing basis for replacing existing energy inefficient, cost ineffective, environmentally detrimental slurry semi-batch reactor-based manufacturing practiced in the pharmaceutical and fine chemicals industries.

  14. Hydrogen production from co-gasification of coal and biomass in supercritical water by continuous flow thermal-catalytic reaction system

    Institute of Scientific and Technical Information of China (English)

    YAN Qiuhui; GUO Liejin; LIANG Xing; ZHANG Ximin

    2007-01-01

    Hydrogen is a clean energy carrier.Converting abundant coal sources and green biomass energy into hydrogen effectively and without any pollution promotes environmental protection.The co-gasification performance of coal and a model compound of biomass,carboxymethylcellulose (CMC)in supercritical water (SCW),were investigated experimentally.The influences of temperature,pressure and concentration on hydrogen production from co-gasification of coal and CMC in SCW under the given conditions (20-25 MPa,650℃,15-30 s) are discussed in detail.The experimental results show that H2,CO2 and CH4 are the main gas products,and the molar fraction of hydrogen reaches in excess of 60%.The higher pressure and higher CMC content facilitate hydrogen production;production is decreased remarkably given a longer residence time.

  15. Heterogeneous catalytic hydrogenation reactions in continuous-flow reactors.

    Science.gov (United States)

    Irfan, Muhammad; Glasnov, Toma N; Kappe, C Oliver

    2011-03-21

    Microreactor technology and continuous flow processing in general are key features in making organic synthesis both more economical and environmentally friendly. Heterogeneous catalytic hydrogenation reactions under continuous flow conditions offer significant benefits compared to batch processes which are related to the unique gas-liquid-solid triphasic reaction conditions present in these transformations. In this review article recent developments in continuous flow heterogeneous catalytic hydrogenation reactions using molecular hydrogen are summarized. Available flow hydrogenation techniques, reactors, commonly used catalysts and examples of synthetic applications with an emphasis on laboratory-scale flow hydrogenation reactions are presented.

  16. Numerical Study of Passive Catalytic Recombiner for Hydrogen Mitigation

    Directory of Open Access Journals (Sweden)

    Pavan K Sharma

    2010-10-01

    Full Text Available A significant amount of hydrogen is expected to be released within the containment of a water cooled power reactor after a severe accident. To reduce the risk of deflagration/detonation various means for hydrogen control have been adopted all over the world. Passive catalytic recombiner with vertical flat catalytic plate is one of such hydrogen mitigating device. Passive catalytic recombiners are designed for the removal of hydrogen generated in order to limit the impact of possible hydrogen combustion. Inside a passive catalytic recombiner, numerous thin steel sheets coated with catalyst material are vertically arranged at the bottom opening of a sheet metal housing forming parallel flow channels for the surrounding gas atmosphere. Already below conventional flammability limits, hydrogen and oxygen react exothermally on the catalytic surfaces forming harmless steam. Detailed numerical simulations and experiments are required for an in-depth knowledge of such plate type catalytic recombiners. Specific finite volume based in-house CFD code has been developed to model and analyse the working of these recombiner. The code has been used to simulate the recombiner device used in the Gx-test series of Battelle-Model Containment (B-MC experiments. The present paper briefly describes the working principle of such passive catalytic recombiner and salient feature of the CFD model developed at Bhabha Atomic Research Centre (BARC. Finally results of the calculations and comparison with existing data are discussed.

  17. Storage of hydrogen in floating catalytic carbon nanotubes after graphitizing

    Institute of Scientific and Technical Information of China (English)

    朱宏伟; 李雪松; 慈立杰; 徐才录; 毛宗强; 梁吉; 吴德海

    2002-01-01

    Hydrogen storage under moderate pressure (~10 Mpa) and ambient temperature (~25℃) in multi-walled carbon nanotubes (MWNTs) prepared by the floating catalyst method is investigated. The capacity of hydrogen adsorption is evaluated based on both the nanotubes diameter and morphology. Indirect evidence indicates that hydrogen adsorption not only occurs on tube surface and interiors, but also in tube interlayers. The results show that the floating catalytic carbon nanotubes might be a candidate hydrogen storage material for fuel cell electric vehicles.

  18. Co/ZnO and Ni/ZnO catalysts for hydrogen production by bioethanol steam reforming. Influence of ZnO support morphology on the catalytic properties of Co and Ni active phases

    Energy Technology Data Exchange (ETDEWEB)

    Da Costa-Serra, J.F.; Chica, A. [Instituto de Tecnolgia Quimica (UPV-CSIC), Universidad Politecnica de Valencia, Consejo Superior de Investigaciones Cientificas, Avenida de los naranjos s/n, 46022 Valencia (Spain); Guil-Lopez, R. [Instituto de Catalisis y Petroleoquimica, CSIC, Marie Curie 2, Cantoblanco, 28049 Madrid (Spain)

    2010-07-15

    Renewable hydrogen production from steam reforming of bioethanol is an interesting approach to produce sustainable hydrogen. However, simultaneous competitive reactions can occur, decreasing the hydrogen production yield. To overcome this problem, modifications in the steam reforming catalysts are being studied. Ni and Co active phases supported over modified ZnO have been widely studied in hydrogen production from steam reforming of bioethanol. However, the influence of the morphology and particle size of ZnO supports on the catalytic behaviour of the supported Ni and Co has not been reported. In the present work, we show how the morphology, shape, and size of ZnO support particles can control the impregnation process of the metal active centres, which manages the properties of active metallic particles. It has been found that nanorod particles of ZnO, obtained by calcination of Zn acetate, favour the metal-support interactions, decreasing the metallic particle sizes and avoiding metal (Co or Ni) sinterization during the calcination of metal precursors. Small metallic particle sizes lead to high values of active metal exposure surface, increasing the bioethanol conversion and hydrogen production. (author)

  19. Biological hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Benemann, J.R. [Univ. of California, Berkeley, CA (United States)

    1995-11-01

    Biological hydrogen production can be accomplished by either thermochemical (gasification) conversion of woody biomass and agricultural residues or by microbiological processes that yield hydrogen gas from organic wastes or water. Biomass gasification is a well established technology; however, the synthesis gas produced, a mixture of CO and H{sub 2}, requires a shift reaction to convert the CO to H{sub 2}. Microbiological processes can carry out this reaction more efficiently than conventional catalysts, and may be more appropriate for the relatively small-scale of biomass gasification processes. Development of a microbial shift reaction may be a near-term practical application of microbial hydrogen production.

  20. Short hydrogen bonds in the catalytic mechanism of serine proteases

    Directory of Open Access Journals (Sweden)

    VLADIMIR LESKOVAC

    2008-04-01

    Full Text Available The survey of crystallographic data from the Protein Data Bank for 37 structures of trypsin and other serine proteases at a resolution of 0.78–1.28 Å revealed the presence of hydrogen bonds in the active site of the enzymes, which are formed between the catalytic histidine and aspartate residues and are on average 2.7 Å long. This is the typical bond length for normal hydrogen bonds. The geometric properties of the hydrogen bonds in the active site indicate that the H atom is not centered between the heteroatoms of the catalytic histidine and aspartate residues in the active site. Taken together, these findings exclude the possibility that short “low-barrier” hydrogen bonds are formed in the ground state structure of the active sites examined in this work. Some time ago, it was suggested by Cleland that the “low-barrier hydrogen bond” hypothesis is operative in the catalytic mechanism of serine proteases, and requires the presence of short hydrogen bonds around 2.4 Å long in the active site, with the H atom centered between the catalytic heteroatoms. The conclusions drawn from this work do not exclude the validity of the “low-barrier hydrogen bond” hypothesis at all, but they merely do not support it in this particular case, with this particular class of enzymes.

  1. Preparation, structural characterization and catalytic properties of Co/CeO2 catalysts for the steam reforming of ethanol and hydrogen production

    Science.gov (United States)

    Lovón, Adriana S. P.; Lovón-Quintana, Juan J.; Almerindo, Gizelle I.; Valença, Gustavo P.; Bernardi, Maria I. B.; Araújo, Vinícius D.; Rodrigues, Thenner S.; Robles-Dutenhefner, Patrícia A.; Fajardo, Humberto V.

    2012-10-01

    In this paper, Co/CeO2 catalysts, with different cobalt contents were prepared by the polymeric precursor method and were evaluated for the steam reforming of ethanol. The catalysts were characterized by N2 physisorption (BET method), X-ray diffraction (XRD), UV-visible diffuse reflectance, temperature programmed reduction analysis (TPR) and field emission scanning electron microscopy (FEG-SEM). It was observed that the catalytic behavior could be influenced by the experimental conditions and the nature of the catalyst employed. Physical-chemical characterizations revealed that the cobalt content of the catalyst influences the metal-support interaction which results in distinct catalyst performances. The catalyst with the highest cobalt content showed the best performance among the catalysts tested, exhibiting complete ethanol conversion, hydrogen selectivity close to 66% and good stability at a reaction temperature of 600 °C.

  2. A novel liquid organic hydrogen carrier system based on catalytic peptide formation and hydrogenation.

    Science.gov (United States)

    Hu, Peng; Fogler, Eran; Diskin-Posner, Yael; Iron, Mark A; Milstein, David

    2015-04-17

    Hydrogen is an efficient green fuel, but its low energy density when stored under high pressure or cryogenically, and safety issues, presents significant disadvantages; hence finding efficient and safe hydrogen carriers is a major challenge. Of special interest are liquid organic hydrogen carriers (LOHCs), which can be readily loaded and unloaded with considerable amounts of hydrogen. However, disadvantages include high hydrogen pressure requirements, high reaction temperatures for both hydrogenation and dehydrogenation steps, which require different catalysts, and high LOHC cost. Here we present a readily reversible LOHC system based on catalytic peptide formation and hydrogenation, using an inexpensive, safe and abundant organic compound with high potential capacity to store and release hydrogen, applying the same catalyst for loading and unloading hydrogen under relatively mild conditions. Mechanistic insight of the catalytic reaction is provided. We believe that these findings may lead to the development of an inexpensive, safe and clean liquid hydrogen carrier system.

  3. Photoelectrochemical hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Rocheleau, R.; Misra, A.; Miller, E. [Univ. of Hawaii, Honolulu, HI (United States)

    1998-08-01

    A significant component of the US DOE Hydrogen Program is the development of a practical technology for the direct production of hydrogen using a renewable source of energy. High efficiency photoelectrochemical systems to produce hydrogen directly from water using sunlight as the energy source represent one of the technologies identified by DOE to meet this mission. Reactor modeling and experiments conducted at UH provide strong evidence that direct solar-to-hydrogen conversion efficiency greater than 10% can be expected using photoelectrodes fabricated from low-cost, multijunction (MJ) amorphous silicon solar cells. Solar-to-hydrogen conversion efficiencies as high as 7.8% have been achieved using a 10.3% efficient MJ amorphous silicon solar cell. Higher efficiency can be expected with the use of higher efficiency solar cells, further improvement of the thin film oxidation and reduction catalysts, and optimization of the solar cell for hydrogen production rather than electricity production. Hydrogen and oxygen catalysts developed under this project are very stable, exhibiting no measurable degradation in KOH after over 13,000 hours of operation. Additional research is needed to fully optimize the transparent, conducting coatings which will be needed for large area integrated arrays. To date, the best protection has been afforded by wide bandgap amorphous silicon carbide films.

  4. Biomimetic hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Krassen, Henning

    2009-05-15

    Hydrogenases catalyze the reduction of protons to molecular hydrogen with outstanding efficiency. An electrode surface which is covered with active hydrogenase molecules becomes a promising alternative to platinum for electrochemical hydrogen production. To immobilize the hydrogenase on the electrode, the gold surface was modified by heterobifunctional molecules. A thiol headgroup on one side allowed the binding to the gold surface and the formation of a self-assembled monolayer. The other side of the molecules provided a surface with a high affinity for the hydrogenase CrHydA1 from Chlamydomonas reinhardtii. With methylviologen as a soluble energy carrier, electrons were transferred from carboxy-terminated electrodes to CrHydA1 and conducted to the active site (H-cluster), where they reduce protons to molecular hydrogen. A combined approach of surface-enhanced infrared absorption spectroscopy, gas chromatography, and surface plasmon resonance allowed quantifying the hydrogen production on a molecular level. Hydrogen was produced with a rate of 85 mol H{sub 2} min{sup -1} mol{sup -1}. On a 1'- benzyl-4,4'-bipyridinum (BBP)-terminated surface, the electrons were mediated by the monolayer and no soluble electron carrier was necessary to achieve a comparable hydrogen production rate (approximately 50% of the former system). The hydrogen evolution potential was determined to be -335 mV for the BBP-bound hydrogenase and -290 mV for the hydrogenase which was immobilized on a carboxy-terminated mercaptopropionic acid SAM. Therefore, both systems significantly reduce the hydrogen production overpotential and allow electrochemical hydrogen production at an energy level which is close to the commercially applied platinum electrodes (hydrogen evolution potential of -270 mV). In order to couple hydrogen production and photosynthesis, photosystem I (PS1) from Synechocystis PCC 6803 and membrane-bound hydrogenase (MBH) from Ralstonia eutropha were bound to each other

  5. Hybrid catalytic-DBD plasma reactor for the production of hydrogen and preferential CO oxidation (CO-PROX) at reduced temperatures.

    Science.gov (United States)

    Rico, Víctor J; Hueso, José L; Cotrino, José; Gallardo, Victoria; Sarmiento, Belén; Brey, Javier J; González-Elipe, Agustín R

    2009-11-07

    Dielectric Barrier Discharges (DBD) operated at atmospheric pressure and working at reduced temperatures (T < 115 degrees C) and a copper-manganese oxide catalyst are combined for the direct decomposition and the steam reforming of methanol (SRM) for hydrogen production and for the preferential oxidation of CO (CO-PROX).

  6. Liquid-phase chemical hydrogen storage: catalytic hydrogen generation under ambient conditions.

    Science.gov (United States)

    Jiang, Hai-Long; Singh, Sanjay Kumar; Yan, Jun-Min; Zhang, Xin-Bo; Xu, Qiang

    2010-05-25

    There is a demand for a sufficient and sustainable energy supply. Hence, the search for applicable hydrogen storage materials is extremely important owing to the diversified merits of hydrogen energy. Lithium and sodium borohydride, ammonia borane, hydrazine, and formic acid have been extensively investigated as promising hydrogen storage materials based on their relatively high hydrogen content. Significant advances, such as hydrogen generation temperatures and reaction kinetics, have been made in the catalytic hydrolysis of aqueous lithium and sodium borohydride and ammonia borane as well as in the catalytic decomposition of hydrous hydrazine and formic acid. In this Minireview we briefly survey the research progresses in catalytic hydrogen generation from these liquid-phase chemical hydrogen storage materials.

  7. Electrocatalytic hydrogenation of organic molecules on conductive new catalytic material

    Energy Technology Data Exchange (ETDEWEB)

    Tountian, D. [Louis Pasteur Univ., Strasbourg (France). Laboratoire d' Electrochimie et de Chimie Physique du Corps Solide; Sherbrooke Univ., Sherbrooke, PQ (Canada). Dept. de Chimie, Centre de Recherche en Electrochimie et Electrocatalyse; Brisach-Wittmeyer, A.; Menard, H. [Sherbrooke Univ., Sherbrooke, PQ (Canada). Dept. de Chimie, Centre de Recherche en Electrochimie et Electrocatalyse; Nkeng, P.; Poillerat, G. [Louis Pasteur Univ., Strasbourg (France). Laboratoire d' Electrochimie et de Chimie Physique du Corps Solide

    2008-07-01

    Electrocatalytic hydrogenation (ECH) of organic molecules is a process where chemisorbed hydrogen is produced by electroreduction of water which reacts with the species in bulk. Greater emphasis is being placed on improving the nature of the building material of the electrodes in order to increase ECH efficiency. The effectiveness of the ECH is known to be linked to the nature of electrode materials used and their adsorption properties. This work presented the effect of conductive support material on ECH. The conductive catalysts were obtained from tin dioxide which is chemically stable. Palladium was the catalytic metal used in this study. The production of chemisorbed hydrogen was shown to depend on the quantity of metallic nanoaggregates in electrical contact with the reticulated vitreous carbon use as electrode. The conductive support, F-doped tin dioxide, was obtained by the sol-gel method. The electrocatalysts were characterized by different methods as resistivity measurements, linear sweep voltammetry, XRD, SEM, TGA/DSC, and FTIR analysis. The effects of temperature and time of calcination were also investigated. The study showed that the F-doped SnO2 electrocatalyst appeared to increase the rate of phenol electrohydrogenation. It was concluded that the improved electrocatalytic activity of Pd/F-doped SnO2 can be attributed to the simultaneous polarization of all the metallic Pd nanoaggregates present on the surface as well as in the pores of the matrix by contact with RVC. This results in a better production of chemisorbed atomic hydrogen with a large number of adlienation points. 9 refs., 3 figs.

  8. Sustainable Electrochemical Hydrogen Production

    DEFF Research Database (Denmark)

    Kibsgaard, Jakob; Jaramillo, Thomas F.; Chorkendorff, Ib

    production is through electrochemical processes coupled to renewable energy sources such as wind or solar. The hydrogen evolution reaction (HER, 2H+ + 2e− → H2) constitutes half of the water splitting reaction. To increase process efficiency, active catalysts for the HER are needed. Currently platinum...

  9. Development of catalytic hydrogenation reactors for the fine chemicals industry

    NARCIS (Netherlands)

    Westerterp, K.R.; Gelder, van K.B.; Janssen, H.J.; Oyevaar, M.H.

    1988-01-01

    A survey is given of the problems to be solved before catalytic hydrogenation reactors can be applied in a multiproduct plant in which selectivity problems are experienced. Some results are reported on work done on the reaction kinetics of two multistep model reactions and on mathematical modelling

  10. Asymmetric Catalytic Hydrogenation Using Rhodium Diphosphinites Derived From D-glucose and D-mannitol

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Three diphosphinites were synthesized for preparing rhodium-diphosphinite complexes. The complexes were used for asymmetric catalytic hydrogenation of amino acid precursor a -acetamidocinnamic acid and its methyl ester. With all complexes, D-amino acid is the most abundant product.

  11. Synthesis of Ultraviolet Absorber Benzotriazole by Nanoparticles Ag/SiO2 Catalytic Hydrogenation

    Institute of Scientific and Technical Information of China (English)

    QI Gang; ZHANG Wen-Guo; DAI Yong

    2012-01-01

    The Ag/SiO2 nanoparticles had been successfully synthesized. The Ag/SiO2 nano- particles can be an excellent catalyst for the synthesis of ultraviolet absorber benzotriazole by catalytic hydrogenation. The synthesis route is very efficient with less pollution and excellent yields. It is also easy to industrialized production.

  12. Photoelectrochemical Hydrogen Production

    CERN Document Server

    Krol, R van de

    2012-01-01

    Photoelectrochemical Hydrogen Production describes the principles and materials challenges for the conversion of sunlight into hydrogen through water splitting at a semiconducting electrode. Readers will find an analysis of the solid state properties and materials requirements for semiconducting photo-electrodes, a detailed description of the semiconductor/electrolyte interface, in addition to the photo-electrochemical (PEC) cell. Experimental techniques to investigate both materials and PEC device performance are outlined, followed by an overview of the current state-of-the-art in PEC materia

  13. Catalytic wet hydrogen peroxide oxidation of a petrochemical wastewater.

    Science.gov (United States)

    Pariente, M I; Melero, J A; Martínez, F; Botas, J A; Gallego, A I

    2010-01-01

    Continuous Catalytic Wet Hydrogen Peroxide Oxidation (CWHPO) for the treatment of a petrochemical industry wastewater has been studied on a pilot plant scale process. The installation, based on a catalytic fixed bed reactor (FBR) coupled with a stirred tank reactor (STR), shows an interesting alternative for the intensification of a continuous CWHPO treatment. Agglomerated SBA-15 silica-supported iron oxide (Fe(2)O(3)/SBA-15) was used as Fenton-like catalyst. Several variables such as the temperature and hydrogen peroxide concentration, as well as the capacity of the pilot plant for the treatment of inlet polluted streams with different dilution degrees were studied. Remarkable results in terms of TOC reduction and increased biodegradability were achieved using 160 degrees C and moderate hydrogen peroxide initial concentration. Additionally, a good stability of the catalyst was evidenced for 8 hours of treatment with low iron leaching (less than 1 mg/L) under the best operating conditions.

  14. Photovoltaic hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Hiser, H.W.; Memory, S.B.; Veziroglu, T.N.; Padin, J. [Univ. of Miami, Coral Gables, FL (United States)

    1996-10-01

    This is a new project, which started in June 1995, and involves photovoltaic hydrogen production as a fuel production method for the future. In order to increase the hydrogen yield, it was decided to use hybrid solar collectors to generate D.C. electricity, as well as high temperature steam for input to the electrolyzer. In this way, some of the energy needed to dissociate the water is supplied in the form of heat (or low grade energy), to generate steam, which results in a reduction of electrical energy (or high grade energy) needed. As a result, solar to hydrogen conversion efficiency is increased. In the above stated system, the collector location, the collector tracking sub-system (i.e., orientation/rotation), and the steam temperature have been taken as variables. Five locations selected - in order to consider a variety of latitudes, altitudes, cloud coverage and atmospheric conditions - are Atlanta, Denver, Miami, Phoenix and Salt Lake City. Plain PV and hybrid solar collectors for a stationary south facing system and five different collector rotation systems have been analyzed. Steam temperatures have been varied between 200{degrees}C and 1200{degrees}C. During the first year, solar to hydrogen conversion efficiencies have been considered. The results show that higher steam temperatures, 2 dimensional tracking system, higher elevations and dryer climates causes higher conversion efficiencies. Cost effectiveness of the sub-systems and of the overall system will be analyzed during the second year. Also, initial studies will be made of an advanced high efficiency hybrid solar hydrogen production system.

  15. Biomimetic Production of Hydrogen

    Science.gov (United States)

    Gust, Devens

    2004-03-01

    The basic reaction for hydrogen generation is formation of molecular hydrogen from two electrons and two protons. Although there are many possible sources for the protons and electrons, and a variety of mechanisms for providing the requisite energy for hydrogen synthesis, the most abundant and readily available source of protons and electrons is water, and the most attractive source of energy for powering the process is sunlight. Not surprisingly, living systems have evolved to take advantage of these sources for materials and energy. Thus, biology provides paradigms for carrying out the reactions necessary for hydrogen production. Photosynthesis in green plants uses sunlight as the source of energy for the oxidation of water to give molecular oxygen, protons, and reduction potential. Some photosynthetic organisms are capable of using this reduction potential, in the form of the reduced redox protein ferredoxin, to reduce protons and produce molecular hydrogen via the action of an hydrogenase enzyme. A variety of other organisms metabolize the reduced carbon compounds that are ultimately the major products of photosynthesis to produce molecular hydrogen. These facts suggest that it might be possible to use light energy to make molecular hydrogen via biomimetic constructs that employ principles similar to those used by natural organisms, or perhaps with hybrid "bionic" systems that combine biomimetic materials with natural enzymes. It is now possible to construct artificial photosynthetic systems that mimic some of the major steps in the natural process.(1) Artificial antennas based on porphyrins, carotenoids and other chromophores absorb light at various wavelengths in the solar spectrum and transfer the harvested excitation energy to artificial photosynthetic reaction centers.(2) In these centers, photoinduced electron transfer uses the energy from light to move an electron from a donor to an acceptor moiety, generating a high-energy charge-separated state

  16. Preparation of Hydrogen through Catalytic Steam Reforming of Bio-oil

    Institute of Scientific and Technical Information of China (English)

    吴层; 颜涌捷; 李庭琛; 亓伟

    2007-01-01

    Hydrogen was prepared via catalytic steam reforming of bio-oil which was obtained from fast pyrolysis of biomass in a fluidized bed reactor. Influential factors including temperature, weight hourly space velocity (WHSV) of bio-oil, mass ratio of steam to bio-oil (S/B) as well as catalyst type on hydrogen selectivity and other desirable gas products were investigated. Based on hydrogen in stoichiometric potential and carbon balance in gaseous phase and feed, hydrogen yield and carbon selectivity were examined. The experimental results show that higher temperature favors the hydrogen selectivity by H2 mole fraction in gaseous products stream and it plays an important role in hydrogen yield and carbon selectivity. Higher hydrogen selectivity and yield, and carbon selectivity were obtained at lower bio-oil WHSV. In catalytic steam reforming system a maximum steam concentration value exists, at which hydrogen selectivity and yield, and carbon selectivity keep constant. Through experiments, preferential operation conditions were obtained as follows: temperature 800~850℃, bio-oil WHSV below 3.0 h-1, and mass ratio of steam to bio-oil 10~12. The performance tests indicate that Ni-based catalysts are optional, especially Ni/a-Al2O3 effective in the steam reforming process.

  17. Catalytic hydrogen evolution by polyaminoacids using mercury electrode

    Directory of Open Access Journals (Sweden)

    Marko Živanovič

    2010-12-01

    Full Text Available It was shown that using constant current chronopotentiometricstripping (CPS peptides and proteins at nanomolar concentrations produce protein structure–sensitive peak H at mercury electrodes. This peak is due to the catalytic hydrogen evolution reaction (HER. Polyamino acids can be considered as an intermediate model system between peptides and macromolecular proteins. Here we used polyamino acids (poly(aa such as polylysine (polyLys and polyarginine (polyArg and cyclic voltammetry or CPS in combination with hanging mercury drop electrode to explore how different amino acid residues in proteins contribute to the catalyticHER.

  18. Waste/By-Product Hydrogen

    Science.gov (United States)

    2011-01-13

    By‐ product Hydrogen Fuel Flexibility Biogas : generated from organic waste �Wastewater treatment plants can provide multiple MW of renewable... Waste /By product Hydrogen Waste H2 sources include: � Waste bio‐mass: biogas to high temp fuel cells to produce H2 – there are over two dozen sites...13 Waste /By product Hydrogen ‐ Biogas

  19. Catalytic efficiency of Nb and Nb oxides for hydrogen dissociation

    Energy Technology Data Exchange (ETDEWEB)

    Isobe, Shigehito, E-mail: isobe@eng.hokudai.ac.jp [Graduate School of Engineering, Hokkaido University, N-13, W-8, Sapporo 060-0813 (Japan); Creative Research Institution, Hokkaido University, N-20, W-10, Sapporo 001-0021 (Japan); Kudoh, Katsuhiro; Hino, Satoshi; Hashimoto, Naoyuki; Ohnuki, Somei [Graduate School of Engineering, Hokkaido University, N-13, W-8, Sapporo 060-0813 (Japan); Hara, Kenji [Catalysis Research Center, Hokkaido University, N-20, W-10, Sapporo 001-0021 (Japan)

    2015-08-24

    In this letter, catalytic efficiency of Nb, NbO, Nb{sub 2}O{sub 3}, NbO{sub 2}, and Nb{sub 2}O{sub 5} for dissociation and recombination of hydrogen were experimentally investigated. On the surface of Nb and Nb oxides in a gas mixture of H{sub 2} and D{sub 2}, H{sub 2} and D{sub 2} molecules can be dissociated to H and D atoms; then, H{sub 2}, D{sub 2}, and HD molecules can be produced according to the law of probability. With increase of frequency of the dissociation and recombination, HD ratio increases. The ratio of H{sub 2} and HD gas was analyzed by quadrupole mass spectrometry. As a result, NbO showed the highest catalytic activity towards hydrogen dissociation and recombination.

  20. CATALYTIC HYDROGENATION AND OXIDATION OF BIOMASS-DERIVED LEVULINIC ACID

    Directory of Open Access Journals (Sweden)

    Yan Gong

    2011-02-01

    Full Text Available Levulinic acid (LA, 4-oxo-pentanoic acid, is a new platform chemical with various potential uses. In this paper, catalytic hydrogenation and oxidation of levulinic acid were studied. It was shown from experiments that levulinic acid can be hydrogenated to γ-valerolactone (GVL over transition metal catalysts and oxidative-decarboxylated to 2-butanone (methyl-ethyl-ketone, MEK and methyl-vinyl-ketone (MVK by cupric oxide (CuO, cupric oxide/cerium oxide (CuO/CeO2, cupric oxide/ alumina (CuO/ Al2O3, and silver(I/ peroxydisulfate (Ag(I/S2O82-.

  1. Catalytic Combustion for Ultra-Low NOx Hydrogen Turbines

    Energy Technology Data Exchange (ETDEWEB)

    Etemad, Shahrokh; Baird, Benjamin; Alavandi, Sandeep

    2011-06-30

    Precision Combustion, Inc., (PCI) in close collaboration with Solar Turbines, Incorporated, has developed and demonstrated a combustion system for hydrogen fueled turbines that reduces NOx to low single digit level while maintaining or improving current levels of efficiency and eliminating emissions of carbon dioxide. Full scale Rich Catalytic Hydrogen (RCH1) injector was developed and successfully tested at Solar Turbines, Incorporated high pressure test facility demonstrating low single digit NOx emissions for hydrogen fuel in the range of 2200F-2750F. This development work was based on initial subscale development for faster turnaround and reduced cost. Subscale testing provided promising results for 42% and 52% H2 with NOx emissions of less than 2 ppm with improved flame stability. In addition, catalytic reactor element testing for substrate oxidation, thermal cyclic injector testing to simulate start-stop operation in a gas turbine environment, and steady state 15 atm. operation testing were performed successfully. The testing demonstrated stable and robust catalytic element component life for gas turbine conditions. The benefit of the catalytic hydrogen combustor technology includes capability of delivering near-zero NOx without costly post-combustion controls and without requirement for added sulfur control. In addition, reduced acoustics increase gas turbine component life. These advantages advances Department of Energy (DOE’s) objectives for achievement of low single digit NOx emissions, improvement in efficiency vs. postcombustion controls, fuel flexibility, a significant net reduction in Integrated Gasification Combined Cycle (IGCC) system net capital and operating costs, and a route to commercialization across the power generation field from micro turbines to industrial and utility turbines.

  2. Hydrogen-based tubular catalytic membrane for removing nitrate from groundwater.

    Science.gov (United States)

    Chen, Y X; Zhang, Y; Liu, H Y; Sharma, K R; Chen, G H

    2004-02-01

    A porous tubular ceramic membrane coated with palladium-cupper (Pd-Cu) catalyst on its surface was prepared and evaluated for catalytic reduction of nitrate from groundwater. Nitrate reduction activity and selectivity with the catalytic membrane were compared with Pd-Cu/Al2O3 catalyst particles. The catalytic membrane reactor exhibited a better selectivity by enabling an effective control of hydrogen gas, thus minimizing ammonium production. No leaching of palladium and copper into aqueous phase was observed, thereby indicating a high chemical stability of the metallic ions on the carrier support. This was also evidenced by the X-ray photoelectron spectroscopy (XPS) profiles of fresh and used catalysts, which showed no significant difference in surface compositions. Due to its higher selectivity in nitrate reduction and better flexibility in terms of operating conditions, the tubular catalytic ceramic membrane could be useful in removing nitrate from groundwater.

  3. Characteristics of La-modified Ni-Al2O3 and Ni-SiO2 catalysts for COx-free hydrogen production by catalytic decomposition of methane

    Institute of Scientific and Technical Information of China (English)

    Chatla; Anjaneyulu; Velisoju; Vijay; Kumar; Suresh; K.Bhargava; Akula; Venugopal

    2013-01-01

    Hydrotalcite precursors of La modified Ni-Al2O3 and Ni-SiO2 catalysts prepared by co-precipitation method and the catalytic activities were examined for the production of COx-free H2 by CH4 decomposition. Physico-chemical characteristics of fresh, reduced and used catalysts were evaluated by XRD, TPR and O2 pulse chemisorptions, TEM and BET-SA techniques. XRD studies showed phases due to hydrotalcite-like precursors in oven dried form produced dispersed NiO species upon calcination in static air above 450 C. Raman spectra of deactivated samples revealed the presence of both ordered and disordered forms of carbon. Ni-La-Al2O3catalyst with a mole ratio of Ni : La : Al = 2 : 0.1 : 0.9 exhibited tremendously high longevity with a hydrogen production rate of 1300 molH2 mol 1 Ni. A direct relationship between Ni metal surface area and hydrogen yields was established.

  4. Hydrogenation of o-cresol on platinum catalyst: Catalytic experiments and first-principles calculations

    Science.gov (United States)

    Li, Yaping; Liu, Zhimin; Xue, Wenhua; Crossley, Steven P.; Jentoft, Friederike C.; Wang, Sanwu

    2017-01-01

    Catalytic experiments were performed for the hydrogenation of o-cresol in n-dodecane over a platinum catalyst. Batch reactions analyzed with an in-situ ATR IR probe suggest that the hydrogenation results in the formation of the final product, 2-methyl-cyclohexanol, with 2-methyl-cyclohexanone as the intermediate product. Ab initio density-functional theory was employed to investigate the atomic-scale mechanism of o-cresol hydrogenation on the Pt(111) surface. The formation of 2-methyl-cyclohexanone was found to involve two steps. The first step is a hydrogen abstraction, that is, the H atom in the hydroxyl group migrates to the Pt surface. The second step is hydrogenation, that is, the pre-existing H atoms on Pt react with the carbon atoms in the aromatic ring. On the other hand, 2-methyl-cyclohexanonol may be produced through two paths, with activation energies slightly greater than that for the formation of 2-methyl-cyclohexanone. One path involves direct hydrogenation of the aromatic ring. Another path involves three steps, with the partial hydrogenation of the ring as the first step, hydrogen abstraction of the sbnd OH group as the second, and hydrogenation of remaining C atoms and the O atom the last.

  5. Catalytic production of conjugated fatty acids and oils.

    Science.gov (United States)

    Philippaerts, An; Goossens, Steven; Jacobs, Pierre A; Sels, Bert F

    2011-06-20

    The reactive double bonds in conjugated vegetable oils are of high interest in industry. Traditionally, conjugated vegetable oils are added to paints, varnishes, and inks to improve their drying properties, while recently there is an increased interest in their use in the production of bioplastics. Besides the industrial applications, also food manufactures are interested in conjugated vegetable oils due to their various positive health effects. While the isomer type is less important for their industrial purposes, the beneficial health effects are mainly associated with the c9,t11, t10,c12 and t9,t11 CLA isomers. The production of CLA-enriched oils as additives in functional foods thus requires a high CLA isomer selectivity. Currently, CLAs are produced by conjugation of oils high in linoleic acid, for example soybean and safflower oil, using homogeneous bases. Although high CLA productivities and very high isomer selectivities are obtained, this process faces many ecological drawbacks. Moreover, CLA-enriched oils can not be produced directly with the homogeneous bases. Literature reports describe many catalytic processes to conjugate linoleic acid, linoleic acid methyl ester, and vegetable oils rich in linoleic acid: biocatalysts, for example enzymes and cells; metal catalysts, for example homogeneous metal complexes and heterogeneous catalysts; and photocatalysts. This Review discusses state-of-the-art catalytic processes in comparison with some new catalytic production routes. For each category of catalytic process, the CLA productivities and the CLA isomer selectivity are compared. Heterogeneous catalysis seems the most attractive approach for CLA production due to its easy recovery process, provided that the competing hydrogenation reaction is limited and the CLA production rate competes with the current homogeneous base catalysis. The most important criteria to obtain high CLA productivity and isomer selectivity are (1) absence of a hydrogen donor, (2

  6. Catalytic hydrogen peroxide decomposition on La1-xSrxCo03-d perovskite oxides

    NARCIS (Netherlands)

    Dam, Van-Ahn. T.; Olthuis, W.; Bergveld, P.; Berg, van den A.

    2005-01-01

    Lanthanide perovskite oxides are mentioned as material for hydrogen peroxide sensor because they can catalytically decompose hydrogen peroxide in an aqueous medium. The catalytic properties of these perovskite oxides to hydrogen peroxide are suggested due to their oxygen vacancies influenced by the

  7. Formic Acid Free Flowsheet Development To Eliminate Catalytic Hydrogen Generation In The Defense Waste Processing

    Energy Technology Data Exchange (ETDEWEB)

    Lambert, Dan P.; Stone, Michael E.; Newell, J. David; Fellinger, Terri L.; Bricker, Jonathan M.

    2012-09-14

    The Defense Waste Processing Facility (DWPF) processes legacy nuclear waste generated at the Savannah River Site (SRS) during production of plutonium and tritium demanded by the Cold War. The nuclear waste is first treated via a complex sequence of controlled chemical reactions and then vitrified into a borosilicate glass form and poured into stainless steel canisters. Converting the nuclear waste into borosilicate glass canisters is a safe, effective way to reduce the volume of the waste and stabilize the radionuclides. Testing was initiated to determine whether the elimination of formic acid from the DWPF's chemical processing flowsheet would eliminate catalytic hydrogen generation. Historically, hydrogen is generated in chemical processing of alkaline High Level Waste sludge in DWPF. In current processing, sludge is combined with nitric and formic acid to neutralize the waste, reduce mercury and manganese, destroy nitrite, and modify (thin) the slurry rheology. The noble metal catalyzed formic acid decomposition produces hydrogen and carbon dioxide. Elimination of formic acid by replacement with glycolic acid has the potential to eliminate the production of catalytic hydrogen. Flowsheet testing was performed to develop the nitric-glycolic acid flowsheet as an alternative to the nitric-formic flowsheet currently being processed at the DWPF. This new flowsheet has shown that mercury can be reduced and removed by steam stripping in DWPF with no catalytic hydrogen generation. All processing objectives were also met, including greatly reducing the Slurry Mix Evaporator (SME) product yield stress as compared to the baseline nitric/formic flowsheet. Ten DWPF tests were performed with nonradioactive simulants designed to cover a broad compositional range. No hydrogen was generated in testing without formic acid.

  8. A Au/Cu2O-TiO2 system for photo-catalytic hydrogen production. A pn-junction effect or a simple case of in situ reduction?

    KAUST Repository

    Sinatra, Lutfan

    2015-02-01

    Photo-catalytic H2 production from water has been studied over Au-Cu2O nanoparticle deposited on TiO2 (anatase) in order to probe into both the plasmon resonance effect (Au nanoparticles) and the pn-junction at the Cu2O-TiO2 interface. The Au-Cu2O composite is in the form of ∼10 nm Au nanoparticles grown on ∼475 nm Cu2O octahedral nanocrystals with (111) facets by partial galvanic replacement. X-ray Photoelectron Spectroscopy (XPS) Cu2p and Auger L3M4,5M4,5 lines indicate that the surface of Cu2O is mainly composed of Cu+. The rate for H2 production (from 95 water/5 ethylene glycol; vol.%) over 2 wt.% (Au/Cu2O)-TiO2 is found to be ∼10 times faster than that on 2 wt.% Au-TiO2 alone. Raman spectroscopy before and after reaction showed the disappearance of Cu+ lines (2Eu) at 220 cm-1. These observations coupled with the induction time observed for the reaction rate suggest that in situ reduction from Cu+ to Cu0 occurs upon photo-excitation. The reduction requires the presence of TiO2 (electron transfer). The prolonged activity of the reaction (with no signs of deactivation) despite the reduction to Cu0 indicates that the latter takes part in the reaction by providing additional sites for the reaction, most likely as recombination centers for hydrogen atoms to form molecular hydrogen. This phenomenon provides an additional route for enhancing the efficiency and lifetime of Cu2O-TiO2 photocatalytic systems, beyond the usually ascribed pn-junction effect.

  9. Microstructured reactors for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Aartun, Ingrid

    2005-07-01

    Small scale hydrogen production by partial oxidation (POX) and oxidative steam reforming (OSR) have been studied over Rh-impregnated microchannel Fecralloy reactors and alumina foams. Trying to establish whether metallic microchannel reactors have special advantages for hydrogen production via catalytic POX or OSR with respect to activity, selectivity and stability was of special interest. The microchannel Fecralloy reactors were oxidised at 1000 deg C to form a {alpha}-Al2O3 layer in the channels in order to enhance the surface area prior to impregnation. Kr-BET measurements showed that the specific surface area after oxidation was approximately 10 times higher than the calculated geometric surface area. Approximately 1 mg Rh was deposited in the channels by impregnation with an aqueous solution of RhCl3. Annular pieces (15 mm o.d.,4 mm i.d., 14 mm length) of extruded {alpha}-Al2O3 foams were impregnated with aqueous solutions of Rh(NO3)3 to obtain 0.01, 0.05 and 0.1 wt.% loadings, as predicted by solution uptake. ICP-AES analyses showed that the actual Rh loadings probably were higher, 0.025, 0.077 and 0.169 wt.% respectively. One of the microchannel Fecralloy reactors and all Al2O3 foams were equipped with a channel to allow for temperature measurement inside the catalytic system. Temperature profiles obtained along the reactor axes show that the metallic microchannel reactor is able to minimize temperature gradients as compared to the alumina foams. At sufficiently high furnace temperature, the gas phase in front of the Rh/Al2O3/Frecralloy microchannel reactor and the 0.025 wt.% Rh/Al2O3 foams ignites. Gas phase ignition leads to lower syngas selectivity and higher selectivity to total oxidation products and hydrocarbon by-products. Before ignition of the gas phase the hydrogen selectivity is increased in OSR as compared to POX, the main contribution being the water-gas shift reaction. After gas phase ignition, increased formation of hydrocarbon by-products

  10. Catalytic Hydrogenation Reaction of Naringin-Chalcone. Study of the Electrochemical Reaction

    Directory of Open Access Journals (Sweden)

    B. A. López de Mishima

    2000-03-01

    Full Text Available The electrocatalytic hydrogenation reaction of naringin derivated chalcone is studied. The reaction is carried out with different catalysts in order to compare with the classic catalytic hydrogenation.

  11. CATALYTIC HYDROGENATION OF ACRYLATE ASMMETRIC Dd(Ⅱ)—CHELATING RESINS CONTAINING AMINO ACID LIGANDS

    Institute of Scientific and Technical Information of China (English)

    Wangying; WangHongzuo; 等

    1995-01-01

    The catalytic hydrogenation of palladium chelating resins containing chiral amino acid ligands based on lower crosslinked poly(chloroethyl acrylate) and some effects on the rate of hydrogenation were studied.

  12. Simple and rapid hydrogenation of p-nitrophenol with aqueous formic acid in catalytic flow reactors

    Directory of Open Access Journals (Sweden)

    Rahat Javaid

    2013-06-01

    Full Text Available The inner surface of a metallic tube (i.d. 0.5 mm was coated with a palladium (Pd-based thin metallic layer by flow electroless plating. Simultaneous plating of Pd and silver (Ag from their electroless-plating solution produced a mixed distributed bimetallic layer. Preferential acid leaching of Ag from the Pd–Ag layer produced a porous Pd surface. Hydrogenation of p-nitrophenol was examined in the presence of formic acid simply by passing the reaction solution through the catalytic tubular reactors. p-Aminophenol was the sole product of hydrogenation. No side reaction occurred. Reaction conversion with respect to p-nitrophenol was dependent on the catalyst layer type, the temperature, pH, amount of formic acid, and the residence time. A porous and oxidized Pd (PdO surface gave the best reaction conversion among the catalytic reactors examined. p-Nitrophenol was converted quantitatively to p-aminophenol within 15 s of residence time in the porous PdO reactor at 40 °C. Evolution of carbon dioxide (CO2 was observed during the reaction, although hydrogen (H2 was not found in the gas phase. Dehydrogenation of formic acid did not occur to any practical degree in the absence of p-nitrophenol. Consequently, the nitro group was reduced via hydrogen transfer from formic acid to p-nitrophenol and not by hydrogen generated by dehydrogenation of formic acid.

  13. Liquid-Phase Catalytic Hydrogenation of Furfural in Variable Solvent Media

    Institute of Scientific and Technical Information of China (English)

    夏淑倩; 李阳; 商巧燕; 张成武; 马沛生

    2016-01-01

    Water is the most abundant compound inherently existing in bio-oils. Thus understanding the role of water within bio-oils upgrading process is essential for future engineering scale-up design. In this study, furfural was chosen as bio-oils model compound, and the catalytic hydrogenation of furfural over commercial 5%, Ru/C catalyst was firstly investigated in a series of gradient variable water/ethanol mixture solvents. Water had a signifi-cant effect on the distribution of product yields. The dominant reaction pathways varied with the water contents in the water/ethanol mixture solvents. Typically, when ethanol was used as the solvent, the main products were ob-tained by the hydrogenation of carbonyl group or furan ring. When pure water was used as the solvent, the rear-rangement reaction of furfural to cyclopentanone should be selectively promoted theoretically. However, serious polymerization and resinification were observed herein in catalytic hydrogenation system of pure water. The cata-lyst surface was modified by the water-insoluble polymers, and consequently, a relative low yield of cyclopenta-none was obtained. A plausible multiple competitive reaction mechanism between polymerization reaction and the hydrogenation of furfural was suggested in this study. Characterizations(TG,FT-IR,SEM)were employed to analyze and explain our experiments.

  14. Fusion Energy for Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Fillo, J. A.; Powell, J. R.; Steinberg, M.; Salzano, F.; Benenati, R.; Dang, V.; Fogelson, S.; Isaacs, H.; Kouts, H.; Kushner, M.; Lazareth, O.; Majeski, S.; Makowitz, H.; Sheehan, T. V.

    1978-09-01

    The decreasing availability of fossil fuels emphasizes the need to develop systems which will produce synthetic fuel to substitute for and supplement the natural supply. An important first step in the synthesis of liquid and gaseous fuels is the production of hydrogen. Thermonuclear fusion offers an inexhaustible source of energy for the production of hydrogen from water. Depending on design, electric generation efficiencies of approximately 40 to 60% and hydrogen production efficiencies by high temperature electrolysis of approximately 50 to 70% are projected for fusion reactors using high temperature blankets.

  15. Hydrogen Production by Thermophilic Fermentation

    NARCIS (Netherlands)

    Niel, van E.W.J.; Willquist, K.; Zeidan, A.A.; Vrije, de T.; Mars, A.E.; Claassen, P.A.M.

    2012-01-01

    Of the many ways hydrogen can be produced, this chapter focuses on biological hydrogen production by thermophilic bacteria and archaea in dark fermentations. The thermophiles are held as promising candidates for a cost-effective fermentation process, because of their relatively high yields and broad

  16. Influence of catalytic systems on process of model object hydrogenation

    Institute of Scientific and Technical Information of China (English)

    Murzabek Ispolovich Baikenov; Gulzhan Gausilevna Baikenova; Bolat Shaimenovich Sarsembayev; Alma Baimagambetova Tateeva; Almas Tusipkhan; Aisha Zharasovna Matayeva

    2014-01-01

    On the basis of b-FeOOH, Fe(OA)3, Fe3O4 iron and spherical catalysts NiO/SiO2, Fe2O3/SiO2 derived from slag waste coals of heating electrical stations, the hydrogenation of model polycyclic hydrocarbon at presence of nan-odimensioned catalysts antracene was studied. On the example of conversion of anthracene, it was shown that upon release of hydrogenation of the product yield and degradation of polycyclic hydrocarbons in the hydrogenation, the mentioned catalyst systems appeared to be in the following order:nanoparticles b-FeOOH, Fe(OA)3 and Fe3O4[spherical catalysts NiO/SiO2, Fe2O3/SiO2[commercial cobalt-molybdenum catalyst. The results showed that the catalysts studied are promising catalysts for the hydrogenation of polycyclic hydrocarbons and may be used for direct coal liquefaction.

  17. High Selective Determination of Anionic Surfactant Using Its Parallel Catalytic Hydrogen Wave

    Institute of Scientific and Technical Information of China (English)

    过玮; 何盈盈; 宋俊峰

    2003-01-01

    A faradaic response of anionic surfactants (AS), such as linear aikylbenzene sulfonate (LAS), dodecyl benzene sulfonate and dodecyl sulfate, was observed in weak acidic medium. The faradaic response of AS includes (1) a catalytic hydrogen wave of AS in HAc/NaAc buffer that was attributed to the reduction of proton associated with the sulfo-group of AS, and (2) a parallel catalytic hydrogen wave of AS in the presence of hydrogen peroxide, which was due to the catalysis of the catalytic hydrogen wave of AS by hydroxyl radical OH electrogenerated in the reduction of hydrogen peroxide. The parallel catalytic hydrogen wave is about 50 times as sensitive as the catalytic hydrogen wave. Based on the parallel catalytic hydrogen wave, a high selective method for the determination of AS was developed. In 0.1mol/L HAc/NaAc (pH=6.2±0.1)/1.0×10-3mol/L H2O2 supporting electrolyte, the second-order derivative peak current of the parallel catalytic hydrogen wave located at-1.33 V (vs. SCE) was rectilinear to AS concentration in the range of 3.0×10-6-2.5×10-4mol/L, without the interference of other surfactants. The proposed method was evaluated by quantitative analysis of AS in environmental wastewater.

  18. Hydrogen Production Technical Team Roadmap

    Energy Technology Data Exchange (ETDEWEB)

    None

    2013-06-01

    The Hydrogen Production Technical Team Roadmap identifies research pathways leading to hydrogen production technologies that produce near-zero net greenhouse gas (GHG) emissions from highly efficient and diverse renewable energy sources. This roadmap focuses on initial development of the technologies, identifies their gaps and barriers, and describes activities by various U.S. Department of Energy (DOE) offices to address the key issues and challenges.

  19. Technical Analysis of Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Ali T-Raissi

    2005-01-14

    The aim of this work was to assess issues of cost, and performance associated with the production and storage of hydrogen via following three feedstocks: sub-quality natural gas (SQNG), ammonia (NH{sub 3}), and water. Three technology areas were considered: (1) Hydrogen production utilizing SQNG resources, (2) Hydrogen storage in ammonia and amine-borane complexes for fuel cell applications, and (3) Hydrogen from solar thermochemical cycles for splitting water. This report summarizes our findings with the following objectives: Technoeconomic analysis of the feasibility of the technology areas 1-3; Evaluation of the hydrogen production cost by technology areas 1; and Feasibility of ammonia and/or amine-borane complexes (technology areas 2) as a means of hydrogen storage on-board fuel cell powered vehicles. For each technology area, we reviewed the open literature with respect to the following criteria: process efficiency, cost, safety, and ease of implementation and impact of the latest materials innovations, if any. We employed various process analysis platforms including FactSage chemical equilibrium software and Aspen Technologies AspenPlus and HYSYS chemical process simulation programs for determining the performance of the prospective hydrogen production processes.

  20. Catalytic hydrogenation of cyclic carbonates: a practical approach from CO2 and epoxides to methanol and diols.

    Science.gov (United States)

    Han, Zhaobin; Rong, Liangce; Wu, Jiang; Zhang, Lei; Wang, Zheng; Ding, Kuiling

    2012-12-21

    Two birds with one stone: the simultaneous production of two important bulk chemicals, methanol and ethylene glycol, from CO(2) and ethylene oxide has been achieved under mild conditions by the highly efficient homogeneous catalytic hydrogenation of ethylene carbonate in the presence of a (PNP)Ru(II) catalyst.

  1. Biological hydrogen production from phytomass

    Energy Technology Data Exchange (ETDEWEB)

    Bartacek, J.; Zabranska, J. [Inst. of Chemical Technology, Prague (Czech Republic). Dept. of Water Technology and Environmental Engineering

    2004-07-01

    Renewable sources of energy have received wide attention lately. One candidate is hydrogen which has the added advantage of involving no greenhouse gases. Biological hydrogen production from wastewater or biowastes is a very attractive production technique. So far, most studies have concentrated on the use of photosynthetic bacteria. However, dark fermentation has recently become a popular topic of research as it has the advantage of not requiring light energy input, something that limits the performance of the photosynthetic method. While pure cultures have been used in most of the investigations to date, in industrial situations mixed cultures will probably be the norm because of unavoidable contamination. In this investigation the phytomass of amaranth (Amaranthus cruentus L) was used to produce hydrogen. Specific organic loading, organic loading, and pH were varied to study the effect on hydrogen production. 18 refs., 1 tab., 6 figs.

  2. Novel catalytic and mechanistic studies on wastewater denitrification with hydrogen.

    Science.gov (United States)

    Theologides, C P; Olympiou, G G; Savva, P G; Pantelidou, N A; Constantinou, B K; Chatziiona, V K; Valanidou, L Y; Piskopianou, C T; Costa, C N

    2014-01-01

    The present work reports up-to-date information regarding the reaction mechanism of the catalytic hydrogenation of nitrates in water media. In the present mechanistic study, an attempt is made, for the first time, to elucidate the crucial role of several catalysts and reaction parameters in the mechanism of the NO(3)(-)/H(2) reaction. Steady-state isotopic transient kinetic analysis (SSITKA) experiments coupled with ex situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) were performed on supported Pd-Cu catalysts for the NO(3)(-)/H(2) and NO(3)(-)/H(2)/O(2) reactions. The latter experiments revealed that the formation and surface coverage of various adsorbed active intermediate N-species on the support or Pd/Cu metal surface is significantly favored in the presence of TiO(2) in the support mixture and in the presence of oxygen in the reaction's gaseous feed stream. The differences in the reactivity of these adsorbed N-species, found in the present work, adequately explain the large effect of the chemical composition of the support and the gas feed composition on catalyst behaviour (activity and selectivity). The present study leads to solid mechanistic evidence concerning the presence of a hydrogen spillover process from the metal to the support. Moreover, this study shows that Cu clusters are active sites for the reduction of nitrates to nitrites.

  3. Recent advances in catalytic asymmetric hydrogenation:Renaissance of the monodentate phosphorus ligands

    Institute of Scientific and Technical Information of China (English)

    GUO Hongchao; DING Kuiling; DAI Lixin

    2004-01-01

    The history for the development of chiral phosphorus ligands in catalytic asymmetric hydrogenation is briefly highlighted. This review focuses on the recent advances in the synthesis of the monodentate phosphorus ligands and their applications in catalytic asymmetric hydrogenation. The examples highlighted in this article clearly demonstrated the importance and advantages of monodentate phosphorus ligands, which had been ignored for 30 a and experienced a renaissance at the very beginning of this millennium, particularly in the area of asymmetric hydrogenation.

  4. Catalytic Hydrogenation of Bio-Oil for Chemicals and Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Elliott, Douglas C.

    2006-02-14

    The scope of work includes optimizing processing conditions and demonstrating catalyst lifetime for catalyst formulations that are readily scaleable to commercial operations. We use a bench-scale, continuous-flow, packed-bed, catalytic, tubular reactor, which can be operated in the range of 100-400 mL/hr., from 50-400 C and up to 20MPa (see Figure 1). With this unit we produce upgraded bio-oil from whole bio-oil or useful bio-oil fractions, specifically pyrolytic lignin. The product oils are fractionated, for example by distillation, for recovery of chemical product streams. Other products from our tests have been used in further testing in petroleum refining technology at UOP and fractionation for product recovery in our own lab. Further scale-up of the technology is envisioned and we will carry out or support process design efforts with industrial partners, such as UOP.

  5. Hydrogen production from solar energy

    Science.gov (United States)

    Eisenstadt, M. M.; Cox, K. E.

    1975-01-01

    Three alternatives for hydrogen production from solar energy have been analyzed on both efficiency and economic grounds. The analysis shows that the alternative using solar energy followed by thermochemical decomposition of water to produce hydrogen is the optimum one. The other schemes considered were the direct conversion of solar energy to electricity by silicon cells and water electrolysis, and the use of solar energy to power a vapor cycle followed by electrical generation and electrolysis. The capital cost of hydrogen via the thermochemical alternative was estimated at $575/kW of hydrogen output or $3.15/million Btu. Although this cost appears high when compared with hydrogen from other primary energy sources or from fossil fuel, environmental and social costs which favor solar energy may prove this scheme feasible in the future.

  6. Low temperature catalytic reforming of heptane to hydrogen and syngas

    Directory of Open Access Journals (Sweden)

    M.E.E. Abashar

    2016-09-01

    Full Text Available The production of hydrogen and syngas from heptane at a low temperature is studied in a circulating fast fluidized bed membrane reactor (CFFBMR. A thin film of palladium-based membrane is employed to the displacement of the thermodynamic equilibrium for high conversion and yield. A mathematical model is developed to simulate the reformer. A substantial improvement of the CFFBMR is achieved by implementing the thin hydrogen membrane. The results showed that almost complete conversion of heptane and 46.25% increase of exit hydrogen yield over the value without membrane are achieved. Also a wide range of the H2/CO ratio within the recommended industrial range is obtained. The phenomena of high spikes of maximum nature at the beginning of the CFFBMR are observed and explanation offered. The sensitivity analysis results have shown that the increase of the steam to carbon feed ratio can increase the exit hydrogen yield up to 108.29%. It was found that the increase of reaction side pressure at a high steam to carbon feed ratio can increase further the exit hydrogen yield by 49.36% at a shorter reactor length. Moreover, the increase of reaction side pressure has an important impact in a significant decrease of the carbon dioxide and this is a positive sign for clean environment.

  7. Negative hydrogen ion production mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Bacal, M. [UPMC, LPP, Ecole Polytechnique, UMR CNRS 7648, Palaiseau (France); Wada, M. [School of Science and Engineering, Doshisha University, Kyoto 610-0321 (Japan)

    2015-06-15

    Negative hydrogen/deuterium ions can be formed by processes occurring in the plasma volume and on surfaces facing the plasma. The principal mechanisms leading to the formation of these negative ions are dissociative electron attachment to ro-vibrationally excited hydrogen/deuterium molecules when the reaction takes place in the plasma volume, and the direct electron transfer from the low work function metal surface to the hydrogen/deuterium atoms when formation occurs on the surface. The existing theoretical models and reported experimental results on these two mechanisms are summarized. Performance of the negative hydrogen/deuterium ion sources that emerged from studies of these mechanisms is reviewed. Contemporary negative ion sources do not have negative ion production electrodes of original surface type sources but are operated with caesium with their structures nearly identical to volume production type sources. Reasons for enhanced negative ion current due to caesium addition to these sources are discussed.

  8. Negative hydrogen ion production mechanisms

    Science.gov (United States)

    Bacal, M.; Wada, M.

    2015-06-01

    Negative hydrogen/deuterium ions can be formed by processes occurring in the plasma volume and on surfaces facing the plasma. The principal mechanisms leading to the formation of these negative ions are dissociative electron attachment to ro-vibrationally excited hydrogen/deuterium molecules when the reaction takes place in the plasma volume, and the direct electron transfer from the low work function metal surface to the hydrogen/deuterium atoms when formation occurs on the surface. The existing theoretical models and reported experimental results on these two mechanisms are summarized. Performance of the negative hydrogen/deuterium ion sources that emerged from studies of these mechanisms is reviewed. Contemporary negative ion sources do not have negative ion production electrodes of original surface type sources but are operated with caesium with their structures nearly identical to volume production type sources. Reasons for enhanced negative ion current due to caesium addition to these sources are discussed.

  9. Microwave Hydrogen Production from Methane

    Science.gov (United States)

    2012-04-01

    Reaction 2 to H2/CO2 products according to Reaction 3 at temperatures in the range of 200-400 °C in the presence of an iron-chromium or copper alloys...hydrogen for a 5-kW fuel cell system. The capital and operating costs of the technology will be estimated and compared to compressed hydrogen delivery and onsite electrolysis .

  10. Solar Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Koval, C. [Univ. of Colorado, Boulder (United States); Sutin, N. [Brookhaven National Lab., Upton, NY (United States); Turner, J. [National Renewable Energy Lab., Golden, CO (United States)

    1996-09-01

    This panel addressed different methods for the photoassisted dissociation of water into its component parts, hydrogen and oxygen. Systems considered include PV-electrolysis, photoelectrochemical cells, and transition-metal based microheterogeneous and homogeneous systems. While none of the systems for water splitting appear economically viable at the present time, the panel identified areas of basic research that could increase the overall efficiency and decrease the costs. Common to all the areas considered was the underlying belief that the water-to-hydrogen half reaction is reasonably well characterized, while the four-electron oxidation of water-to-oxygen is less well understood and represents a significant energy loss. For electrolysis, research in electrocatalysis to reduce overvoltage losses was identified as a key area for increased efficiency. Non-noble metal catalysts and less expensive components would reduce capital costs. While potentially offering higher efficiencies and lower costs, photoelectrochemical-based direct conversion systems undergo corrosion reactions and often have poor energetics for the water reaction. Research is needed to understand the factors that control the interfacial energetics and the photoinduced corrosion. Multi-photon devices were identified as promising systems for high efficiency conversion.

  11. Catalytic Hydrogenation of Organic Compounds without H2 Supply: An Electrochemical System

    Science.gov (United States)

    Navarro, Daniela Maria do Amaral Ferraz; Navarro, Marcelo

    2004-01-01

    An experiment developed for an undergraduate organic chemistry laboratory course that can be used to introduce the catalytic hydrogenation reaction, catalysis electrochemical principles and gas chromatography is presented. The organic compounds hydrogenated by the electrocatalytic hydrogenation (ECH) process were styrene, benzaldehyde and…

  12. Surface Structure and Catalytic Performance of Ni-Fe Catalyst for Low-Temperature CO Hydrogenation

    Directory of Open Access Journals (Sweden)

    Fanhui Meng

    2014-01-01

    Full Text Available Catalysts 16NixFe/Al2O3 (x is 0, 1, 2, 4, 6, 8 were prepared by incipient wetness impregnation method and the catalytic performance for the production of synthetic natural gas (SNG from CO hydrogenation in slurry-bed reactor were studied. The catalysts were characterized by BET, XRD, UV-Vis DRS, H2-TPR, CO-TPD, and XPS, and the results showed that the introduction of iron improved the dispersion of Ni species, weakened the interaction between Ni species and support and decreased the reduction temperature and that catalyst formed Ni-Fe alloy when the content of iron exceeded 2%. Experimental results revealed that the addition of iron to the catalyst can effectively improve the catalytic performance of low-temperature CO methanation. Catalyst 16Ni4Fe/Al2O3 with the iron content of 4% exhibited the best catalytic performance, the conversion of CO and the yield of CH4 reached 97.2% and 84.9%, respectively, and the high catalytic performance of Ni-Fe catalyst was related to the property of formed Ni-Fe alloy. Further increase of iron content led to enhancing the water gas shift reaction.

  13. Biomass Catalytic Pyrolysis with Ni Based Catalyst to Produce Hydrogen Rich Gas

    Institute of Scientific and Technical Information of China (English)

    WANG Mingfeng; LIU Min; XU Xiwei; LI Bosong; ZHANG Qiang; JIAN Enchen

    2010-01-01

    Hydrogen rich gas was produced using rice husk as biomass material on the continuous biomass pyrolysis apparatus which consisted of continuous pyrolysis reactor and secondary catalytic cracking reactor. Ni based catalysts of different Ni/Al mass ratio and calcined temperature were prepared by impregnating method. The catalysts were characterized by X-ray diffraction (XRD),scan electron microscope (SEM) and FT-IR Spectrometer (FT-IR). Ni based catalyst showed good selectivity for H2 production from biomass. Catalysts prepared under different conditions had little influence on the yields of three states products when used at the same cracking temperature. Ni/Al mass ratio played an important role in products selectivity. However, the content of NiO increased further when Ni/Al mass ratio values reached 0.7 : 10, and the yield of H2 slightly increased. Hydrogen yield was greatly impacted by calcined temperature. Catalyst calcined at 550"C performed best. When the catalyst was calcined at high temperature, NiO in the catalyst transformed into NiAl2O4, and the acid site also changed, which caused the deactivation of the catalyst. The hydrogen yield increased with the cracking temperature. The highest stable yield of hydrogen was about 30% without increasing with the cracking temperature.

  14. The hydrogen production; La production d'hydrogene

    Energy Technology Data Exchange (ETDEWEB)

    Aujollet, P.; Goldstein, St. [CEA Cadarach, Dir. de l' Energie Nucleaire, 13 - Saint Paul lez Durance (France); Lucchese, P. [CEA Fontenay aux Roses, Dir. des Nouvelles Technologies de l' Energie, 92 (France)

    2002-07-01

    This paper gives an overview on the implementing of the hydrogen as substitution fuel in the transportation sector. It presents also the problems of this fuel storage and exploitation and describes the production modes and their safety. It also presents the main lines of the japan HTGR program. (A.L.B.)

  15. Novel Applications of the Methyltrioxorhenium/Hydrogen Peroxide Catalytic System

    Energy Technology Data Exchange (ETDEWEB)

    Stankovic, Sasa [Iowa State Univ., Ames, IA (United States)

    2000-09-12

    Methylrhenium trioxide (MTO), CH3Re03, was first prepared in 1979. An improved synthetic route to MTO was devised from dirhenium heptoxide and tetramethyltin in the presence of hexafluoro glutaric anhydride was reported by Herrmann in 1992. During the course of research on this dissertation we uncovered other reactions where the presence or absence of pyridine can, in some cases dramatically, affect the reaction outcome. This dissertation consists of four chapters. The first two chapters deal with the ,oxidation of water sensitive olefinic compounds with the hydrogen perox’ide/MTO system. Chapters 111 and IV focus on the oxidation of hydrazones with the same catalytic system. Chapter I has been published in The Journal of Organic Chemistry and Chapter III in Chemical Communications. Chapters II and IV have been submitted for publication in The Journal of Organic Chemistry. Each section is selfcontained with its own equations, tables, figures and references. All of the work in this dissertation was performed by this author.

  16. Photoelectrochemical Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Jian

    2013-12-23

    The objectives of this project, covering two phases and an additional extension phase, were the development of thin film-based hybrid photovoltaic (PV)/photoelectrochemical (PEC) devices for solar-powered water splitting. The hybrid device, comprising a low-cost photoactive material integrated with amorphous silicon (a-Si:H or a-Si in short)-based solar cells as a driver, should be able to produce hydrogen with a 5% solar-to-hydrogen conversion efficiency (STH) and be durable for at least 500 hours. Three thin film material classes were studied and developed under this program: silicon-based compounds, copper chalcopyrite-based compounds, and metal oxides. With the silicon-based compounds, more specifically the amorphous silicon carbide (a-SiC), we achieved a STH efficiency of 3.7% when the photoelectrode was coupled to an a-Si tandem solar cell, and a STH efficiency of 6.1% when using a crystalline Si PV driver. The hybrid PV/a-SiC device tested under a current bias of -3~4 mA/cm{sup 2}, exhibited a durability of up to ~800 hours in 0.25 M H{sub 2}SO{sub 4} electrolyte. Other than the PV driver, the most critical element affecting the photocurrent (and hence the STH efficiency) of the hybrid PV/a-SiC device was the surface energetics at the a-SiC/electrolyte interface. Without surface modification, the photocurrent of the hybrid PEC device was ~1 mA/cm{sup 2} or lower due to a surface barrier that limits the extraction of photogenerated carriers. We conducted an extensive search for suitable surface modification techniques/materials, of which the deposition of low work function metal nanoparticles was the most successful. Metal nanoparticles of ruthenium (Ru), tungsten (W) or titanium (Ti) led to an anodic shift in the onset potential. We have also been able to develop hybrid devices of various configurations in a monolithic fashion and optimized the current matching via altering the energy bandgap and thickness of each constituent cell. As a result, the short

  17. Hydrogen production from glucose in ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Assenbaum, D.W.; Taccardi, N.; Berger, M.E.M.; Boesmann, A.; Enzenberger, F.; Woelfel, R.; Wasserscheid, P. [Erlangen-Nuernberg Univ. (Germany). Lehrstuhl fuer chemische Reaktionstechnik

    2010-07-01

    Depletion of oil and gas reserves and growing global warming concerns have created a world-wide interest in new concepts for future sustainable energy supplies. The development of effective ways to produce hydrogen from biomass is expected to be one important contribution to such a goal [1]. Nowadays, three main processes are considered for future industrial application, namely: gasification of biomass [2], reforming in supercritical water [3] and aqueous phase reforming [4,5]. Other technologies such as enzymatic decomposition of sugars or steam reforming of bio-oils suffer from low hydrogen production rates and/or complex processing requirements and can probably not be considered for industrial applications in the closer future [6,7]. On the other hand, either the gasification of biomass, which is typically carried out at temperatures above 800 C using Ni or Fe catalysts [8,9,10,11], or the reforming in supercritical water, which is typically carried out in presence of Ru catalyst at pressures of 300bar and temperatures ranging from 500 to 700 C [12], suffer of poor energetic efficiency as a lot of energy is required to run the reactions. More recently, an alternative to the two aforementioned high temperature processes has been proposed as ''aqueous phase reforming'' (APR) by Dumesic and coworkers [13,14,15,16,17]. They achieved the reforming of polyols (such as ethylene glycol, glycerol and sorbitol) using heterogeneous catalysts at temperatures between 200 and 250 C and pressure typically between 15-50bar.The temperature level of the reaction allows generating hydrogen with low amounts of CO in a single reactor. The process typically forms 35 % of hydrogen, 40 % of CO2 and 25 % of combined alkanes. The high amount of formed alkanes originates eventually from CO hydrogenation and Fischer-Tropsch (F-T) reaction [18,19,20,21], those are thermodynamically favored in the above mentioned conditions. However, heterogeneously catalyzed APR

  18. Photoelectrochemical Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Jian

    2013-12-23

    The objectives of this project, covering two phases and an additional extension phase, were the development of thin film-based hybrid photovoltaic (PV)/photoelectrochemical (PEC) devices for solar-powered water splitting. The hybrid device, comprising a low-cost photoactive material integrated with amorphous silicon (a-Si:H or a-Si in short)-based solar cells as a driver, should be able to produce hydrogen with a 5% solar-to-hydrogen conversion efficiency (STH) and be durable for at least 500 hours. Three thin film material classes were studied and developed under this program: silicon-based compounds, copper chalcopyrite-based compounds, and metal oxides. With the silicon-based compounds, more specifically the amorphous silicon carbide (a-SiC), we achieved a STH efficiency of 3.7% when the photoelectrode was coupled to an a-Si tandem solar cell, and a STH efficiency of 6.1% when using a crystalline Si PV driver. The hybrid PV/a-SiC device tested under a current bias of -3~4 mA/cm{sup 2}, exhibited a durability of up to ~800 hours in 0.25 M H{sub 2}SO{sub 4} electrolyte. Other than the PV driver, the most critical element affecting the photocurrent (and hence the STH efficiency) of the hybrid PV/a-SiC device was the surface energetics at the a-SiC/electrolyte interface. Without surface modification, the photocurrent of the hybrid PEC device was ~1 mA/cm{sup 2} or lower due to a surface barrier that limits the extraction of photogenerated carriers. We conducted an extensive search for suitable surface modification techniques/materials, of which the deposition of low work function metal nanoparticles was the most successful. Metal nanoparticles of ruthenium (Ru), tungsten (W) or titanium (Ti) led to an anodic shift in the onset potential. We have also been able to develop hybrid devices of various configurations in a monolithic fashion and optimized the current matching via altering the energy bandgap and thickness of each constituent cell. As a result, the short

  19. Catalytic Hydrogenation over Palladium Complex of Molecular Complex of Poly(4-vinylpyridine) with Acetic Acid

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The palladium complex of the molecular complex of poly(4-vinylpyridine) with acetic acid(PVP/HAc-Pd) was prepared. Its catalytic activity for the hydrogenation of nitrobenzene was found much higher than that of the corresponding palladium complex of poly(4-vinylpyridine). In the presence of a strong inorganic alkali, especially potassium hydroxide, the catalytic activity is greatly improved. The suitable hydrogenation condition for PVP/HAc-Pd is to use 0.1 mol/L ethanol solution of potassium hydroxide as the hydrogenation medium and the hydrogenation is carried out at 45 ℃.

  20. Microbial hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Weaver, P.F.; Maness, P.C.; Martin, S. [National Renewable Energy Lab., Golden, CO (United States)] [and others

    1995-09-01

    Photosynthetic bacteria inhabit an anaerobic or microaerophilic world where H{sub 2} is produced and consumed as a shared intermediary metabolite. Within a given bacterial isolate there are as many as 4 to 6 distinct enzymes that function to evolve or consume H{sub 2}. Three of the H{sub 2}-evolving physiologies involving three different enzymes from photosynthetic bacteria have been examined in detail for commercial viability. Nitrogenase-mediated H{sub 2} production completely dissimilates many soluble organic compounds to H{sub 2} and CO{sub 2} at rates up to 131 {mu}mol H{sub 2}{sm_bullet}min{sup -1}{sm_bullet}g cdw{sup -1} and can remain active for up to 20 days. This metabolism is very energy intensive, however, which limits solar conversion efficiencies. Fermentative hydrogenase can produce H{sub 2} at rates of 440 {mu}mol{sm_bullet}min{sup -1}{sm_bullet}g cdw{sup -1} at low levels of irradiation over indefinite periods. The equilibrium for this activity is low (<0.15 atmospheres), thereby requiring gas sparging, vacuuming, or microbial scavenging to retain prolonged activity. Microbial H{sub 2} production from the CO component of synthesis or producer gases maximally reaches activities of 1.5 mmol{sm_bullet}min{sup -1}{sm_bullet}g cdw{sup -1}. Mass transport of gaseous CO into an aqueous bacterial suspension is the rate-limiting step. Increased gas pressure strongly accelerates these rates. Immobilized bacteria on solid supports at ambient pressures also show enhanced shift activity when the bulk water is drained away. Scaled-up bioreactors with 100-200 cc bed volume have been constructed and tested. The near-term goal of this portion of the project is to engineer and economically evaluate a prototype system for the biological production of H{sub 2} from biomass. The CO shift enables a positive selection technique for O{sub 2}-resistant, H{sub 2}-evolving bacterial enzymes from nature.

  1. Hydrogen Storage and Production Project

    Energy Technology Data Exchange (ETDEWEB)

    Bhattacharyya, Abhijit [Univ. of Arkansas, Little Rock, AR (United States); Biris, A. S. [Univ. of Arkansas, Little Rock, AR (United States); Mazumder, M. K. [Univ. of Arkansas, Little Rock, AR (United States); Karabacak, T. [Univ. of Arkansas, Little Rock, AR (United States); Kannarpady, Ganesh [Univ. of Arkansas, Little Rock, AR (United States); Sharma, R. [Univ. of Arkansas, Little Rock, AR (United States)

    2011-07-31

    This is the final technical report. This report is a summary of the project. The goal of our project is to improve solar-to-hydrogen generation efficiency of the PhotoElectroChemical (PEC) conversion process by developing photoanodes with high absorption efficiency in the visible region of the solar radiation spectrum and to increase photo-corrosion resistance of the electrode for generating hydrogen from water. To meet this goal, we synthesized nanostructured heterogeneous semiconducting photoanodes with a higher light absorption efficiency compared to that of TiO2 and used a corrosion protective layer of TiO2. While the advantages of photoelectrochemical (PEC) production of hydrogen have not yet been realized, the recent developments show emergence of new nanostructural designs of photoanodes and choices of materials with significant gains in photoconversion efficiency.

  2. Production of hydrogen by thermocatalytic cracking of natural gas

    Energy Technology Data Exchange (ETDEWEB)

    Muradov, N.Z. [Univ. of Central Florida, Cape Canaveral, FL (United States)

    1995-09-01

    It is universally accepted that in the next few decades hydrogen production will continue to rely on fossil fuels (primarily, natural gas). On the other hand, the conventional methods of hydrogen production from natural gas (for example, steam reforming) are complex multi-step processes. These processes also result in the emission of large quantities of CO{sub 2} into the atmosphere that produce adverse ecological effects. One alternative is the one-step thermocatalytic cracking (TCC) (or decomposition) of natural gas into hydrogen and carbon. Preliminary analysis indicates that the cost of hydrogen produced by thermal decomposition of natural gas is somewhat lower than the conventional processes after by-product carbon credit is taken. In the short term, this process can be used for on-site production of hydrogen-methane mixtures in gas-filling stations and for CO{sub x}-free production of hydrogen for fuel cell driven prime movers. The experimental data on the thermocatalytic cracking of methane over various catalysts and supports in a wide range of temperatures (500-900{degrees}C) are presented in this paper. Two types of reactors were designed and built at FSEC: continuous flow and pulse fix bed catalytic reactors. The temperature dependence of the hydrogen production yield using oxide type catalysts was studied. Alumina-supported Ni- and Fe-catalysts demonstrated relatively high efficiency in the methane cracking reaction at moderate temperatures (600-800{degrees}C). Kinetic curves of hydrogen production over metal and metal oxide catalysts at different temperatures are presented in the paper. Fe-catalyst demonstrated good stability (for several hours), whereas alumina-supported Pt-catalyst rapidly lost its catalytic activity.

  3. Continuous catalytic hydrogenation of polyaromatic hydrocarbon compounds in hydrogen-supercritical carbon dioxide.

    Science.gov (United States)

    Yuan, Tao; Fournier, Anick R; Proudlock, Raymond; Marshall, William D

    2007-03-15

    A continuous hydrogenation device was evaluated for the detoxification of selected tri-, tetra-, or pentacyclic polyaromatic hydrocarbon (PAH) compounds {anthracene, phenanthrene, chrysene, and benzo[a]pyrene (B[a]P)} by hydrogenation. A substrate stream in hexane, 0.05-1.0% (w/v), was mixed with hydrogen-carbon dioxide (H2-CO2, 5-30% v/v) and delivered to a heated reactor column (25 cm x 1 cm) containing palladium supported on gamma alumina (Pd0/gamma-Al2O3) that was terminated with a capillary restrictor. The flow rate from the reactor, approximately 800 mL min(-1) decompressed gas, corresponded to 4 mL min(-1) fluid under the operating conditions of the trials. Reaction products were recovered by passing the reactor effluent through hexane. At 90 degrees C, the anthracene or phenanthrene substrate was hydrogenated only partially to octahydro and dodecahydro species and contained only a minor quantity of totally hydrogenated products. For substrates with increasing numbers of fused aromatic rings, the hydrogenation efficiency was decreased further. However, at an increasing temperature (90-150 degrees C) and increasing mobile phase flow rate (20.68 MPa corresponding to 2100 mL min(-1) decompressed gas), B[a]P and chrysene were hydrogenated, virtuallytotally, to their corresponding perhydro analogues (eicosahydrobenzo[a]pyrenes and octadecahydrochrysenes), respectively. That this approach might be useful for decontaminating soil extracts was supported by companion in vitro trials in which the substrate and products were assayed for mutagenic activity with five bacterial strains that are auxotrophic for histidine (Salmonella typhimurium TA98, TA100, TA1535, and TA1537) or tryptophan (Escherichia coliWP2 uvrA), using the bacterial reverse mutation assay (modified Ames test). Generally, substantial increases in revertant colony counts were not observed with any of the strains following exposure to the hydrogenation products in the absence or presence of the 10 or 30

  4. Hydrogen Production in Fusion Reactors

    OpenAIRE

    Sudo, S.; Tomita, Y.; Yamaguchi, S.; Iiyoshi, A.; Momota, H; Motojima, O.; Okamoto, M.; Ohnishi, M.; Onozuka, M; Uenosono, C.

    1993-01-01

    As one of methods of innovative energy production in fusion reactors without having a conventional turbine-type generator, an efficient use of radiation produced in a fusion reactor with utilizing semiconductor and supplying clean fuel in a form of hydrogen gas are studied. Taking the candidates of reactors such as a toroidal system and an open system for application of the new concepts, the expected efficiency and a concept of plant system are investigated.

  5. Low Cost Hydrogen Production Platform

    Energy Technology Data Exchange (ETDEWEB)

    Timothy M. Aaron, Jerome T. Jankowiak

    2009-10-16

    A technology and design evaluation was carried out for the development of a turnkey hydrogen production system in the range of 2.4 - 12 kg/h of hydrogen. The design is based on existing SMR technology and existing chemical processes and technologies to meet the design objectives. Consequently, the system design consists of a steam methane reformer, PSA system for hydrogen purification, natural gas compression, steam generation and all components and heat exchangers required for the production of hydrogen. The focus of the program is on packaging, system integration and an overall step change in the cost of capital required for the production of hydrogen at small scale. To assist in this effort, subcontractors were brought in to evaluate the design concepts and to assist in meeting the overall goals of the program. Praxair supplied the overall system and process design and the subcontractors were used to evaluate the components and system from a manufacturing and overall design optimization viewpoint. Design for manufacturing and assembly (DFMA) techniques, computer models and laboratory/full-scale testing of components were utilized to optimize the design during all phases of the design development. Early in the program evaluation, a review of existing Praxair hydrogen facilities showed that over 50% of the installed cost of a SMR based hydrogen plant is associated with the high temperature components (reformer, shift, steam generation, and various high temperature heat exchange). The main effort of the initial phase of the program was to develop an integrated high temperature component for these related functions. Initially, six independent concepts were developed and the processes were modeled to determine overall feasibility. The six concepts were eventually narrowed down to the highest potential concept. A US patent was awarded in February 2009 for the Praxair integrated high temperature component design. A risk analysis of the high temperature component was

  6. Hydrogen Production for Refuelling Applications

    Energy Technology Data Exchange (ETDEWEB)

    Hulteberg, Christian; Aagesen, Diane (Intelligent Energy, Long Beach, CA (United States))

    2009-08-15

    /day); Feedstock Cost (USD 0.15 - USD 0.45 per kg); Availability (85% - 95%). The return-on-investment is between USD 90 000 and USD 180 000 in 60 % of the 5 000 simulation runs, which leads to the conclusion that given these assumptions the owning and operation of such a unit can be profitable. As for the performance of the system, it is concluded to be within targets based on the different performance measures reported above. The conversion is in the expected range (80-85%), given the throughput of 16 kg of hydrogen per day. The efficiency as reported is in the acceptable range (approx65%), with some room for improvement within the given system architecture, if desired. However, there is a trade-off between throughput, efficiency and cost that will have to be considered in every redesign of the system. The PSA chosen for the task has performed well during the 200+ hours of operation and there is no doubt that it will be sufficient for the task. The same thing can be said with respect to the system performance with respect to thermo-mechanical stress; which was proven by operating the system for more than 500 hours and performing 58 start-and-stop cycles during the testing. There does not seem to be any major differences between operating on natural gas or methane, based on the testing performed. The slight decrease in hydrogen production can be due to a difference in the H{sub 2}/CO ratio between the various fuels. As expected the efficiency increases with load as well as the hydrogen production rate. Based on the results disseminated above, there is no indication why the current reactor system cannot be configured into a field deployable system. The operation of the system has given valuable experience that will be embedded into any field deployed unit

  7. Hydrogen production processes; Procedes de production d'hydrogene

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2003-07-01

    The goals of this first Gedepeon workshop on hydrogen production processes are: to stimulate the information exchange about research programs and research advances in the domain of hydrogen production processes, to indicate the domains of interest of these processes and the potentialities linked with the coupling of a nuclear reactor, to establish the actions of common interest for the CEA, the CNRS, and eventually EDF, that can be funded in the framework of the Gedepeon research group. This document gathers the slides of the 17 presentations given at this workshop and dealing with: the H{sub 2} question and the international research programs (Lucchese P.); the CEA's research program (Lucchese P., Anzieu P.); processes based on the iodine/sulfur cycle: efficiency of a facility - flow-sheets, efficiencies, hard points (Borgard J.M.), R and D about the I/S cycle: Bunsen reaction (Colette S.), R and D about the I/S cycle: the HI/I{sub 2}/H{sub 2}O system (Doizi D.), demonstration loop/chemical engineering (Duhamet J.), materials and corrosion (Terlain A.); other processes under study: the Westinghouse cycle (Eysseric C.), other processes under study at the CEA (UT3, plasma,...) (Lemort F.), database about thermochemical cycles (Abanades S.), Zn/ZnO cycle (Broust F.), H{sub 2} production by cracking, high temperature reforming with carbon trapping (Flamant G.), membrane technology (De Lamare J.); high-temperature electrolysis: SOFC used as electrolyzers (Grastien R.); generic aspects linked with hydrogen production: technical-economical evaluation of processes (Werkoff F.), thermodynamic tools (Neveu P.), the reactor-process coupling (Aujollet P.). (J.S.)

  8. SYNTHESIS AND CHARACTERIZATION OF A SILICA-SUPPORTED CARBOXYMETHYLCELLULOSE PLATINUM COMPLEX AND ITS CATALYTIC BEHAVIORS FOR HYDROGENATION OF AROMATICS

    Institute of Scientific and Technical Information of China (English)

    TANG Liming; HUANG Meiyu; JIANG Yingyan

    1996-01-01

    A silica-supported carboxymethylcellulose platinum complex (abbreviated as SiO2-CMC-Pt) has been prepared and characterized by XPS. Its catalytic properties for hydrogenation of aromatic compounds were studied. The results showed that this catalyst could catalyze the hydrogenation of phenol, anisol, p-cresol, benzene and toluene to cyclohexanol, cyclohexyl methyl ether, p-methyl cyclohexanol, cyclohexane and methylcyclohexane, respectively in 100% yield at 30℃ and 1 atm. In the hydrogenation of phenol,COO/Pt ratio in SiO2-CMC-Pt has much influence on the initial hydrogenation rate and the selectivity for the intermediate product, cyclohexanone. The highest initial rate and the highest yield of cyclohexanone both occur at COO/Pt ratio of 6. The complex is stable during the reaction and can be used repeatedly.

  9. Advances in ethanol reforming for the production of hydrogen

    Directory of Open Access Journals (Sweden)

    Laura Guerrero

    2014-06-01

    Full Text Available Catalytic steam reforming of ethanol (SRE is a promising route for the production of renewable hydrogen (H2. This article reviews the influence of doping supported-catalysts used in SRE on the conversion of ethanol, selectivity for H2, and stability during long reaction periods. In addition, promising new technologies such as membrane reactors and electrochemical reforming for performing SRE are presented.

  10. Solar based hydrogen production systems

    CERN Document Server

    Dincer, Ibrahim

    2013-01-01

    This book provides a comprehensive analysis of various solar based hydrogen production systems. The book covers first-law (energy based) and second-law (exergy based) efficiencies and provides a comprehensive understanding of their implications. It will help minimize the widespread misuse of efficiencies among students and researchers in energy field by using an intuitive and unified approach for defining efficiencies. The book gives a clear understanding of the sustainability and environmental impact analysis of the above systems. The book will be particularly useful for a clear understanding

  11. GTI's hydrogen programs: hydrogen production, storage, and applications

    Institute of Scientific and Technical Information of China (English)

    范钦柏

    2006-01-01

    The use of hydrogen as an energy carrier could help address our concerns about energy security, global climate change,and air quality. Fuel cells are an important enabling technology for the Hydrogen Future and have the potential to revolutionize theway we power our nation, offering cleaner, more-efficient alternatives to the combustion of gasoline and other fossil fuels.For over 45 years, GTI has been active in hydrogen energy research, development and demonstration. The Institute has extensive experience and on-going work in all aspects of the hydrogen energy economy including production, delivery, infrastructure,use, safety and public policy. This paper discusses the recent GTI programs in hydrogen production, hydrogen storage, and proton exchange membrane fuel cells (PEMFC) and solid oxide fuel cells (SOFC).

  12. Catalytic nanoreactors in continuous flow: hydrogenation inside single-walled carbon nanotubes using supercritical CO2.

    Science.gov (United States)

    Chamberlain, Thomas W; Earley, James H; Anderson, Daniel P; Khlobystov, Andrei N; Bourne, Richard A

    2014-05-25

    One nanometre wide carbon nanoreactors are utilised as the reaction vessel for catalytic chemical reactions on a preparative scale. Sub-nanometre ruthenium catalytic particles which are encapsulated solely within single-walled carbon nanotubes offering a unique reaction environment are shown to be active when embedded in a supercritical CO2 continuous flow reactor. A range of hydrogenation reactions were tested and the catalyst displayed excellent stability over extended reaction times.

  13. Application of microscopy technology in thermo-catalytic methane decomposition to hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Mei, Irene Lock Sow, E-mail: irene.sowmei@gmail.com; Lock, S. S. M., E-mail: serenelock168@gmail.com; Abdullah, Bawadi, E-mail: bawadi-abdullah@petronas.com.my [Chemical Engineering Department, Universiti Teknologi PETRONAS, Bandar Sri Iskandar, 31750, Perak (Malaysia)

    2015-07-22

    Hydrogen production from the direct thermo-catalytic decomposition of methane is a promising alternative for clean fuel production because it produces pure hydrogen without any CO{sub x} emissions. However, thermal decomposition of methane can hardly be of any practical and empirical interest in the industry unless highly efficient and effective catalysts, in terms of both specific activity and operational lifetime have been developed. In this work, bimetallic Ni-Pd on gamma alumina support have been developed for methane cracking process by using co-precipitation and incipient wetness impregnation method. The calcined catalysts were characterized to determine their morphologies and physico-chemical properties by using Brunauer-Emmett-Teller method, Field Emission Scanning Electron Microscopy, Energy-dispersive X-ray spectroscopy and Thermogravimetric Analysis. The results suggested that that the catalyst which is prepared by the co-precipitation method exhibits homogeneous morphology, higher surface area, have uniform nickel and palladium dispersion and higher thermal stability as compared to the catalyst which is prepared by wet impregnation method. This characteristics are significant to avoid deactivation of the catalysts due to sintering and carbon deposition during methane cracking process.

  14. Catalytic hydrogenation using complexes of base metals with tridentate ligands

    Energy Technology Data Exchange (ETDEWEB)

    Vasudevan, Kalyan V.; Zhang, Guoqi; Hanson, Susan K.

    2016-09-06

    Complexes of cobalt and nickel with tridentate ligand PNHP.sup.R are effective for hydrogenation of unsaturated compounds. Cobalt complex [(PNHP.sup.Cy)Co(CH.sub.2SiMe.sub.3)]BAr.sup.F.sub.4 (PNHP.sup.Cy=bis[2-(dicyclohexylphosphino)ethyl]amine, BAr.sup.F.sub.4=B(3,5-(CF.sub.3).sub.2C.sub.6H.sub.3).sub.4)) was prepared and used with hydrogen for hydrogenation of alkenes, aldehydes, ketones, and imines under mild conditions (25-60.degree. C., 1-4 atm H.sub.2). Nickel complex [(PNHP.sup.Cy)Ni(H)]BPh.sub.4 was used for hydrogenation of styrene and 1-octene under mild conditions. (PNP.sup.Cy)Ni(H) was used for hydrogenating alkenes.

  15. Catalytic hydrogenation using complexes of base metals with tridentate ligands

    Energy Technology Data Exchange (ETDEWEB)

    Hanson, Susan K.; Zhang, Guoqi; Vasudevan, Kalyan V.

    2017-02-14

    Complexes of cobalt and nickel with tridentate ligand PNHP.sup.R are effective for hydrogenation of unsaturated compounds. Cobalt complex [(PNHP.sup.Cy)Co(CH.sub.2SiMe.sub.3)]BAr.sup.F.sub.4 (PNHP.sup.Cy=bis[2-(dicyclohexylphosphino)ethyl]amine, BAr.sup.F.sub.4=B(3,5-(CF.sub.3).sub.2C.sub.6H.sub.3).sub.4)) was prepared and used with hydrogen for hydrogenation of alkenes, aldehydes, ketones, and imines under mild conditions (25-60.degree. C., 1-4 atm H.sub.2). Nickel complex [(PNHP.sup.Cy)Ni(H)]BPh.sub.4 was used for hydrogenation of styrene and 1-octene under mild conditions. (PNP.sup.Cy)Ni(H) was used for hydrogenating alkenes.

  16. Maximizing hydrogen production by cyanobacteria

    Energy Technology Data Exchange (ETDEWEB)

    Bothe, H.; Winkelmann, S.; Boison, G. [Botanical Inst., The Univ. of Cologne, Cologne (Germany)

    2008-03-15

    When incubated anaerobically, in the light, in the presence of C{sub 2}H{sub 2} and high concentrations of H{sub 2}, both Mo-grown Anabaena variabilis and either Mo- or V-grown Anabaena azotica produce large amounts of H{sub 2} in addition to the H{sub 2} initially added. In contrast, C{sub 2}H{sub 2}-reduction is diminished under these conditions. The additional H{sub 2}-production mainly originates from nitrogenase with the V-enzyme being more effective than the Mo-protein. This enhanced H{sub 2}-production in the presence of added H{sub 2} and C{sub 2}H{sub 2} should be of interest in approaches to commercially exploit solar energy conversion by cyanobacterial photosynthesis for the generation of molecular hydrogen as a clean energy source. (orig.)

  17. Dedicated nuclear facilities for electrolytic hydrogen production

    Science.gov (United States)

    Foh, S. E.; Escher, W. J. D.; Donakowski, T. D.

    1979-01-01

    An advanced technology, fully dedicated nuclear-electrolytic hydrogen production facility is presented. This plant will produce hydrogen and oxygen only and no electrical power will be generated for off-plant use. The conceptual design was based on hydrogen production to fill a pipeline at 1000 psi and a 3000 MW nuclear base, and the base-line facility nuclear-to-shaftpower and shaftpower-to-electricity subsystems, the water treatment subsystem, electricity-to-hydrogen subsystem, hydrogen compression, efficiency, and hydrogen production cost are discussed. The final conceptual design integrates a 3000 MWth high-temperature gas-cooled reactor operating at 980 C helium reactor-out temperature, direct dc electricity generation via acyclic generators, and high-current density, high-pressure electrolyzers based on the solid polymer electrolyte approach. All subsystems are close-coupled and optimally interfaced and pipeline hydrogen is produced at 1000 psi. Hydrogen costs were about half of the conventional nuclear electrolysis process.

  18. Hydrogen Generation from Catalytic Steam Reforming of Acetic Acid by Ni/Attapulgite Catalysts

    Directory of Open Access Journals (Sweden)

    Yishuang Wang

    2016-11-01

    Full Text Available In this research, catalytic steam reforming of acetic acid derived from the aqueous portion of bio-oil for hydrogen production was investigated using different Ni/ATC (Attapulgite Clay catalysts prepared by precipitation, impregnation and mechanical blending methods. The fresh and reduced catalysts were characterized by XRD, N2 adsorption–desorption, TEM and temperature program reduction (H2-TPR. The comprehensive results demonstrated that the interaction between active metallic Ni and ATC carrier was significantly improved in Ni/ATC catalyst prepared by precipitation method, from which the mean of Ni particle size was the smallest (~13 nm, resulting in the highest metal dispersion (7.5%. The catalytic performance of the catalysts was evaluated by the process of steam reforming of acetic acid in a fixed-bed reactor under atmospheric pressure at two different temperatures: 550 °C and 650 °C. The test results showed the Ni/ATC prepared by way of precipitation method (PM-Ni/ATC achieved the highest H2 yield of ~82% and a little lower acetic acid conversion efficiency of ~85% than that of Ni/ATC prepared by way of impregnation method (IM-Ni/ATC (~95%. In addition, the deactivation catalysts after reaction for 4 h were analyzed by XRD, TGA-DTG and TEM, which demonstrated the catalyst deactivation was not caused by the amount of carbon deposition, but owed to the significant agglomeration and sintering of Ni particles in the carrier.

  19. Production of hydrogen by thermocatalytic cracking of natural gas

    Energy Technology Data Exchange (ETDEWEB)

    Muradov, N. [Florida Solar Energy Center, Cocoa, FL (United States)

    1996-10-01

    The conventional methods of hydrogen production from natural gas (for example, steam reforming and partial oxidation) are complex, multi-step processes that produce large quantities of CO{sub 2}. The main goal of this project is to develop a technologically simple process for hydrogen production from natural gas (NG) and other hydrocarbon fuels via single-step decomposition of hydrocarbons. This approach eliminates or significantly reduces CO{sub 2} emission. Carbon is a valuable by-product of this process, whereas conventional methods of hydrogen production from NG produce no useful by-products. This approach is based on the use of special catalysts that reduce the maximum temperature of the process from 1400-1500{degrees}C (thermal non-catalytic decomposition of methane) to 500-900{degrees}C. Transition metal based catalysts and various forms of carbon are among the candidate catalysts for the process. This approach can advantageously be used for the development of compact NG reformers for on-site production of hydrogen-methane blends at refueling stations and, also, for the production of hydrogen-rich gas for fuel cell applications. The author extended the search for active methane decomposition catalysts to various modifications of Ni-, Fe-, Mo- and Co-based catalysts. Variation in the operational parameters makes it possible to produce H{sub 2}-CH{sub 4} blends with a wide range of hydrogen concentrations that vary from 15 to 98% by volume. The author found that Ni-based catalysts are more effective at temperatures below 750{degrees}C, whereas Fe-based catalysts are effective at temperatures above 800{degrees}C for the production of hydrogen with purity of 95% v. or higher. The catalytic pyrolysis of liquid hydrocarbons (pentane, gasoline) over Fe-based catalyst was conducted. The author observed the production of a hydrogen-rich gas (hydrogen concentration up to 97% by volume) at a rate of approximately 1L/min.mL of hydrocarbon fuel.

  20. Hydrogen production from microbial strains

    Science.gov (United States)

    Harwood, Caroline S; Rey, Federico E

    2012-09-18

    The present invention is directed to a method of screening microbe strains capable of generating hydrogen. This method involves inoculating one or more microbes in a sample containing cell culture medium to form an inoculated culture medium. The inoculated culture medium is then incubated under hydrogen producing conditions. Once incubating causes the inoculated culture medium to produce hydrogen, microbes in the culture medium are identified as candidate microbe strains capable of generating hydrogen. Methods of producing hydrogen using one or more of the microbial strains identified as well as the hydrogen producing strains themselves are also disclosed.

  1. Potentialities of hydrogen production in Algeria

    Energy Technology Data Exchange (ETDEWEB)

    Boudries, R. [CDER, Route de l' Observatoire, Bouzareah Algiers (Algeria); USTHB, El Alia, Algiers (Algeria); Dizene, R. [USTHB, El Alia, Algiers (Algeria)

    2008-09-15

    The objective of the present study is to estimate the potentialities of hydrogen production in Algeria. Particular attention is paid to the clean and sustainable hydrogen production, i.e., production from renewable energy. First, the present overall energy situation in Algeria is reviewed. Trend in energy demand is analysed taking into account major parameters such as population growth, urbanization, improvement in quality of life and export opportunities. The resources available for hydrogen production are then presented. Finally, the estimation of hydrogen production potential using solar sources, the most important renewable energy sources in Algeria, is presented. This study indicates that the shift to hydrogen economy shows a promising prospect. Not only, it can meet the evergrowing local needs but it will also allow Algeria to keep its share of the energy market. Indeed, as is now the case for natural gas, hydrogen could be delivered to Western Europe through pipelines. (author)

  2. Fermentative hydrogen production by diverse microflora

    Energy Technology Data Exchange (ETDEWEB)

    Baghchehsaraee, B.; Nakhla, G.; Karamanev, D.; Margaritis, A. [Western Ontario Univ., London, ON (Canada). Dept. of Chemical and Biochemical Engineering

    2009-07-01

    This paper presented the results of a study in which hydrogen was produced from activated sludge. This diverse bacterial source has been compared to microflora from anaerobic digester sludge. Batch experiments were conducted at mesophilic (37 degrees C) and thermophilic (55 degrees C) temperatures. The hydrogen production yields with activated sludge at mesophilic and thermophilic temperatures were 0.25 and 0.93 mol H{sub 2}/mol glucose, respectively. The maximum hydrogen production rates with activated sludge in both temperatures were 4.2 mL/h. Anaerobic digester sludge showed higher hydrogen production yields and rates at both mesophilic and thermophilic temperatures. Repeated batch experiments with activated sludge resulted in increased hydrogen production in consecutive batches. However, the formation of lactic acid and ethanol resulted in unstable hydrogen production in the repeated batches.

  3. Development of catalytic systems for selective hydrogenation and hydrogenolysis based on statistical planning methods coupled with kinetic studies

    Energy Technology Data Exchange (ETDEWEB)

    Zhorov, Yu.M.; Morozova, E.V.; Panchenkov, G.M.

    1979-01-01

    An efficient catalyst design methodology is described, which was used in developing an active and stable mixed oxide catalytic composition for selective hydrogenation of m-bonds under conditions excluding hydrogenolysis of C-C bonds. Catalysts of optimum composition, i.e., 40-50Vertical Bar3< CuO/25-30Vertical Bar3< NiO/20-35Vertical Bar3< SiO/sub 2/, and structure (20-30 A. average pore radius) can be prepared by coprecipitation of copper and nickel salts with silica gel powder in a sodium silicate solution at 90/sup 0/C. By using these catalysts, crotonaldehyde (CA) was hydrogenated to n-butanol in one stage with over 99Vertical Bar3< yields at 180/sup 0/C. The same catalyst was efficient in selective hydrogenation of acetylene (contained in relatively high concentrations in pyrolysis gases) to ethylene at 130/sup 0/C, hydrogenation of piperylene (a by-product in isoprene manufacture) to n-pentenes at 160/sup 0/C, with almost 100Vertical Bar3< selectivity, and in hydrogenolysis of C-S and C-N bonds at 290/sup 0/-370/sup 0/C. Catalytic hydrorefining of a gasoline fraction (105/sup 0/-180/sup 0/C bp) at 350/sup 0/C and 40 atm, reduced its sulfur content from 0.03Vertical Bar3< to 0.00001Vertical Bar3<, and completely removed nitrogen.

  4. Hydrogen evolution at catalytically-modified nickel foam in alkaline solution

    Science.gov (United States)

    Pierozynski, Boguslaw; Mikolajczyk, Tomasz; Kowalski, Ireneusz M.

    2014-12-01

    This work reports on hydrogen evolution reaction (HER) studied at catalytically modified nickel foam material. The HER was examined in 0.1 M NaOH solution on as received, as well as for Pd and Ru-activated nickel foam catalyst materials, produced via spontaneous deposition of trace amounts of these elements. Catalytic modification of nickel foam results in significant facilitation of the HER kinetics, as manifested through considerably reduced, a.c. impedance-derived values of charge-transfer resistance parameter and substantially altered Tafel polarization slopes. The presence of catalytic additives is clearly revealed through hydrogen underpotential deposition (H UPD) phenomenon, as well as spectroscopically from SEM (Scanning Electron Microscopy) analysis.

  5. Carbon Dioxide Conversion to Valuable Chemical Products over Composite Catalytic Systems

    Energy Technology Data Exchange (ETDEWEB)

    Dagle, Robert A.; Hu, Jianli; Jones, Susanne B.; Wilcox, Wayne A.; Frye, John G.; White, J. F.; Jiang, Juyuan; Wang, Yong

    2013-05-01

    Presented is an experimental study on catalytic conversion of carbon dioxide into methanol, ethanol and acetic acid. Catalysts having different catalytic functions were synthesized and combined in different ways to enhance selectivity to desired products. The combined catalyst system possessed the following functions: methanol synthesis, Fischer-Tropsch synthesis, water-gas-shift and hydrogenation. Results showed that the methods of integrating these catalytic functions played important role in achieving desired product selectivity. It was speculated that if methanol synthesis sites were located adjacent to the C-C chain growth sites, the formation rate of C2 oxygenates would be enhanced. The advantage of using high temperature methanol catalyst PdZnAl in the combined catalyst system was demonstrated. In the presence of PdZnAl catalyst, the combined catalyst system was stable at temperature of 380oC. It was observed that, at high temperature, kinetics favored oxygenate formation. Results implied that the process can be intensified by operating at high temperature using Pd-based methanol synthesis catalyst. Steam reforming of the byproduct organics was demonstrated as a means to provide supplemental hydrogen. Preliminary process design, simulation, and economic analysis of the proposed CO2 conversion process were carried out. Economic analysis indicates how ethanol production cost was affected by the price of CO2 and hydrogen.

  6. Petroleum Refinery Hydrogen Production Unit: Exergy and Production Cost Evaluation

    Directory of Open Access Journals (Sweden)

    Silvio de Oliveira Júnior

    2008-12-01

    Full Text Available Some specific processes are required to obtain pure hydrogen and the most usual one is natural gas reforming, where natural gas reacts with superheated steam producing H2, CO, CO2 and H2O. This paper presents the exergy and production costs evaluation of a complete hydrogen production unit of a petroleum refinery. The hydrogen production unit analysed in this paper has to supply 550,000 Nm3 of hydrogen per day to purify diesel oil. Based on a synthesis plant of the hydrogen production unit, the exergy efficiency of each component and of the overall plant are calculated. The hydrogen production cost is determined by means of a thermoeconomic analysis in which the equality cost partition method is employed, including capital and operational costs, in order to determine the production cost of hydrogen and other products of the plant.

  7. Low temperature catalytic combustion of natural gas - hydrogen - air mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Newson, E.; Roth, F. von; Hottinger, P.; Truong, T.B. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    The low temperature catalytic combustion of natural gas - air mixtures would allow the development of no-NO{sub x} burners for heating and power applications. Using commercially available catalysts, the room temperature ignition of methane-propane-air mixtures has been shown in laboratory reactors with combustion efficiencies over 95% and maximum temperatures less than 700{sup o}C. After a 500 hour stability test, severe deactivation of both methane and propane oxidation functions was observed. In cooperation with industrial partners, scaleup to 3 kW is being investigated together with startup dynamics and catalyst stability. (author) 3 figs., 3 refs.

  8. Redirection of metabolism for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Harwood, Caroline S.

    2011-11-28

    This project is to develop and apply techniques in metabolic engineering to improve the biocatalytic potential of the bacterium Rhodopseudomonas palustris for nitrogenase-catalyzed hydrogen gas production. R. palustris, is an ideal platform to develop as a biocatalyst for hydrogen gas production because it is an extremely versatile microbe that produces copious amounts of hydrogen by drawing on abundant natural resources of sunlight and biomass. Anoxygenic photosynthetic bacteria, such as R. palustris, generate hydrogen and ammonia during a process known as biological nitrogen fixation. This reaction is catalyzed by the enzyme nitrogenase and normally consumes nitrogen gas, ATP and electrons. The applied use of nitrogenase for hydrogen production is attractive because hydrogen is an obligatory product of this enzyme and is formed as the only product when nitrogen gas is not supplied. Our challenge is to understand the systems biology of R. palustris sufficiently well to be able to engineer cells to produce hydrogen continuously, as fast as possible and with as high a conversion efficiency as possible of light and electron donating substrates. For many experiments we started with a strain of R. palustris that produces hydrogen constitutively under all growth conditions. We then identified metabolic pathways and enzymes important for removal of electrons from electron-donating organic compounds and for their delivery to nitrogenase in whole R. palustris cells. For this we developed and applied improved techniques in 13C metabolic flux analysis. We identified reactions that are important for generating electrons for nitrogenase and that are yield-limiting for hydrogen production. We then increased hydrogen production by blocking alternative electron-utilizing metabolic pathways by mutagenesis. In addition we found that use of non-growing cells as biocatalysts for hydrogen gas production is an attractive option, because cells divert all resources away from growth and

  9. Hydrogen production by alkaline water electrolysis

    OpenAIRE

    Santos, Diogo M. F.; Sequeira,César A. C.; José L. Figueiredo

    2013-01-01

    Water electrolysis is one of the simplest methods used for hydrogen production. It has the advantage of being able to produce hydrogen using only renewable energy. To expand the use of water electrolysis, it is mandatory to reduce energy consumption, cost, and maintenance of current electrolyzers, and, on the other hand, to increase their efficiency, durability, and safety. In this study, modern technologies for hydrogen production by water electrolysis have been investigated. In this article...

  10. Solar Thermochemical Hydrogen Production Plant Design

    OpenAIRE

    Littlefield, Jesse

    2012-01-01

    A plant was designed that uses a solar sulfur-ammonia thermochemical water-splitting cycle for the production of hydrogen. Hydrogen is useful as a fuel for stationary and mobile fuel cells. The chemical process simulator Aspen Plus® was used to model the plant and conduct simulations. The process utilizes the electrolytic oxidation of aqueous ammonium sulfite in the hydrogen production half cycle and the thermal decomposition of molten potassium pyrosulfate and gaseous sulfur trioxide in t...

  11. Molecular catalytic hydrogenation of aromatic hydrocarbons and hydrotreating of coal liquids.

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Shiyong; Stock, L.M.

    1996-05-01

    This report presents the results of research on the development of new catalytic pathways for the hydrogenation of multiring aromatic hydrocarbons and the hydrotreating of coal liquids at The University of Chicago under DOE Contract No. DE-AC22-91PC91056. The work, which is described in three parts, is primarily concerned with the research on the development of new catalytic systems for the hydrogenation of aromatic hydrocarbons and for the improvement of the quality of coal liquids by the addition of dihydrogen. Part A discusses the activation of dihydrogen by very basic molecular reagents to form adducts that can facilitate the reduction of multiring aromatic hydrocarbons. Part B examines the hydrotreating of coal liquids catalyzed by the same base-activated dihydrogen complexes. Part C concerns studies of molecular organometallic catalysts for the hydrogenation of monocyclic aromatic hydrocarbons under mild conditions.

  12. Economics and market potential of hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Swisher, Dr., James; Berger, Dr., Beverly; Fickett, Dr., A.; Dickson, Dr., E.

    1978-09-01

    A study was undertaken to evaluate the economics of producing hydrogen from coal and from water and to assess the market potential for this hydrogen in chemical and fuel applications. Results of this study are summarized. Current chemical applications of hydrogen in manufacturing ammonia and methanol, in refining petroleum and in specialty uses provide a base market for penetration by new hydrogen production technologies, although prospects for the use of hydrogen in fuel applications remain unclear. Electrolysis and coal gasification will be complementary, not competitive, technologies for producing hydrogen. Coal gasification plants are better suited to production of large quantities of hydrogen, while electrolyzers are better suited to the production of hydrogen for small-scale uses. Hydrogen produced through coal gasification may be economical in chemical applications (e.g., ammonia production) by the late 1990's. Development programs now underway are expected to provide new coal gasification technologies with lower first costs and higher efficiencies than current technologies. An on-site coal gasification plant supplying hydrogen in the quantities usually required in chemical applications (from 10 to 100 million cubic feet per day) will be smaller than is generally proposed for syngas plants. Growth in smaller scale specialty uses of hydrogen and improvements in the technology for electrolysis will create conditions favorable to expanded use of hydrogen produced through water electrolysis. The major constraint on use of electrolysis will be the availability of low cost electricity. Shortages of natural gas caused by declining domestic production could induce shifts to producing hydrogen through electrolysis or through coal gasification earlier in time (i.e., the late 1980's or early 1990's) than is suggested by comparative cost calculations alone.

  13. Continuous hydrogen production from organic waste

    Energy Technology Data Exchange (ETDEWEB)

    Noike, T.; Li, Y.Y. [Tohoku Univ., Sendai (Japan). Dept. of Civil Engineering; Ko, I.B. [Cheju National Univ. Jeju (Korea, Republic of). Dept. of Environmental Engineering; Yokoyama, S. [Sanki Engineering CP., Ltd. (Japan); Kohno, Y. [Ex Corporation City and Environmental Planning, Research (Japan)

    2004-07-01

    Hydrogen is seen as a promising fuel for the future. Microbial fermentation of organic wastes is an attractive option. However, it has often been observed that hydrogen production in a continuously-fed reactor stops after a period of time. In this investigation, the effect of pH on lactic acid bacteria in continuous hydrogen production is studied. It was found that the antibiotic effect of the bacteria is prevented by keeping the pH greater than five. To establish what stops continuous hydrogen production, a continuous experiment was run using waste from bean curd manufacturing at a pH of 5.5 and a temperature of 35 degrees celsius. An increase in substrate concentration and the addition of nitrogen preferentially produced acetic and butyric acids and suppressed the production of propionic acid. Because of this, continuous hydrogen production was made possible. 4 refs., 5 tabs., 5 figs.

  14. Hydrogen Recombination Rates of Plate-type Passive Auto-catalytic Recombiner

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jongtae; Hong, Seong-Wan [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Kim, Gun Hong [Kyungwon E-C Co., Seongnam (Korea, Republic of)

    2014-10-15

    The hydrogen mitigation system may include igniters, passive autocatalytic recombiner (PAR), and venting or dilution system. Recently PAR is commonly used as a main component of HMS in a NPP containment because of its passive nature. PARs are categorized by the shape and material of catalytic surface. Catalytic surface coated by platinum is mostly used for the hydrogen recombiners. The shapes of the catalytic surface can be grouped into plate type, honeycomb type and porous media type. Among them, the plate-type PAR is well tested by many experiments. PAR performance analysis can be approached by a multi-scale method which is composed of micro, meso and macro scales. The criterion of the scaling is the ratio of thickness of boundary layer developed on a catalytic surface to representative length of a computational domain. Mass diffusion in the boundary layer must be resolved in the micro scale analysis. In a lumped parameter (LP) analysis using a system code such as MAAP or MELCOR, the chamber of the PAR is much smaller than a computational node. The hydrogen depletion by a PAR is modeled as a source of mass and energy conservation equations. Te catalytic surface reaction of hydrogen must be modeled by a volume-averaged correlation. In this study, a micro scale analysis method is developed using libraries in OpenFOAM to evaluate a hydrogen depletion rate depending on parameters such as size and number of plates and plate arrangement. The analysis code is validated by simulating REKO-3 experiment. And hydrogen depletion analysis is conducted by changing the plate arrangement as a trial of the performance enhancement of a PAR. In this study, a numerical code for an analysis of a PAR performance in a micro scale has been developed by using OpenFOAM libraries. The physical and numerical models were validated by simulating the REKO-3 experiment. As a try to enhance the performance of the plate-type PAR, it was proposed to apply a staggered two-layer arrangement of the

  15. On the mechanism of catalytic hydrogenation of thiophene on hydrogen tungsten bronze.

    Science.gov (United States)

    Xi, Yongjie; Chen, Zhangxian; Gan Wei Kiat, Vincent; Huang, Liang; Cheng, Hansong

    2015-04-21

    Hydrogenation of unsaturated organosulfur compounds is an essential process through which these species are converted into cleaner and more useful compounds. Hydrogen bronze materials have been demonstrated to be efficient catalysts in hydrogenation of simple unsaturated compounds. Herein, we performed density functional theory calculations to investigate hydrogenation of thiophene on hydrogen tungsten bronze. Various reaction pathways were investigated and the most favourable routes were identified. Our results suggest that the reaction proceeds with moderate barriers, and formation of tetrahydrothiophene is facile both thermochemically and kinetically. The present study provides a useful insight into the design of hydrogenation thiophene and its derivatives and effective hydrodesulfurization catalysts.

  16. Hydrogen production through biocatalyzed electrolysis

    NARCIS (Netherlands)

    Rozendal, R.A.

    2007-01-01

    cum laude graduation (with distinction) To replace fossil fuels, society is currently considering alternative clean fuels for transportation. Hydrogen could be such a fuel. In theory, large amounts of renewable hydrogen can be produced from organic contaminants in wastewater. During his PhD research

  17. Scenarios of hydrogen production from wind power

    Energy Technology Data Exchange (ETDEWEB)

    Klaric, Mario

    2010-09-15

    Since almost total amount of hydrogen is currently being produced from natural gas, other ways of cleaner and 'more renewable' production should be made feasible in order to make benchmarks for total 'hydrogen economy'. Hydrogen production from wind power combined with electrolysis imposes as one possible framework for new economy development. In this paper various wind-to-hydrogen scenarios were calculated. Cash flows of asset based project financing were used as decision making tool. Most important parameters were identified and strategies for further research and development and resource allocation are suggested.

  18. Bioreactor design for photofermentative hydrogen production.

    Science.gov (United States)

    Uyar, Basar

    2016-09-01

    Hydrogen will become a significant fuel in the near future. Photofermentative production of hydrogen is a promising and sustainable process. The design, construction and successful operation of the photobioreactors are of critical importance for photofermentative hydrogen production and became a major field of research where novel technologies are developed and adapted frequently. This paper gives an overview of the design aspects related to photobioreactors giving particular attention to design limitations, construction material, type, operating mode and scale-up. Sub-components of the overall system setup such as mixing, temperature control and hydrogen collection are also discussed. Recent achievements in the photobioreactor technologies are described.

  19. Cellular graphene aerogel combines ultralow weight and high mechanical strength: A highly efficient reactor for catalytic hydrogenation.

    Science.gov (United States)

    Zhang, Bingxing; Zhang, Jianling; Sang, Xinxin; Liu, Chengcheng; Luo, Tian; Peng, Li; Han, Buxing; Tan, Xiuniang; Ma, Xue; Wang, Dong; Zhao, Ning

    2016-05-12

    The construction of three-dimensional graphene aerogels (GAs) is of great importance owing to their outstanding properties for various applications. Up to now, the combination of ultralow weight and super mechanical strength for GA remains a great challenge. Here we demonstrate the fabrication of cellular GAs by a facile, easily controlled and versatile route, i.e. the chemical reduction of graphene oxide assemblies at oil-water interface under a mild condition (70 °C). The GA is ultralight (with density <3 mg cm(-3)) yet mechanically resilient because the walls of the cell closely pack in a highly ordered manner to maximize mechanical strength. The GA has been utilized as an appealing reactor for catalytic hydrogenation, which exhibited great advantages such as large oil absorption capability, exceptional catalytic activity, ease of product separation and high stability.

  20. Hydrogen Production by Catalytic Partial Oxidation of Coke Oven Gas in BaCo0.7Fe0.3-xZrxO3-δ Ceramic Membrane Reactors

    Directory of Open Access Journals (Sweden)

    Yao Weilin

    2016-01-01

    Full Text Available The BaCo0.7Fe0.3-xZrxO3-δ (BCFZ, x = 0.04–0.12 mixed ionic–electronic conducting (MIEC membranes were synthesized with a sol–gel method and evaluated as potential membrane reactor materials for the partial oxidation of coke oven gas (COG. The effect of zirconium content on the phase structure, microstructure and performance of the BCFZ membrane under He or COG atmosphere were systemically investigated. The BaCo0.7Fe0.24Zr0.06O3-δ membrane exhibited the best oxygen permeability and good operation stability, which could be a potential candidate of the membrane materials for hydrogen production through the partial oxidation of COG.

  1. CATALYTIC BEHAVIOR OF A SILICA-SUPPORTED POLYTITAZANE-PLATINUM COMPLEX FOR THE HYDROGENATION OF PHENOL

    Institute of Scientific and Technical Information of China (English)

    CHEN Chunwei; HUANG Meiyu; JIANG Yingyan

    1996-01-01

    A new kind of inorganic polymer, viz. silica-supported polytitazane (Ti-N), and its platinum complex (Ti-N-Pt) were prepared. Cyclohexanone can be obtained in a maximum yield of about 62.2% in the hydrogenation of phenol over Ti-N-Pt at room temperature under atmospheric pressure. The effects of mole ratio of N/Pt in the complex, concentration of the catalyst and reaction temperature on the catalytic activity and selectivity have been studied. The complex can be reused several times without loss in its catalytic activity.

  2. Catalytic decomposition of hydrogen peroxide on anthraquinonecyanine and phthalocyanine metal complexes in acid and alkaline electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Pobedinskiy, S.N.; Trofimenko, A.A.; Zharnikova, M.A.

    1985-12-01

    A study of octaoxyanthraquinonecyanines (OOATsM) and phthalocyanines (FTs) of cobalt, iron, and manganese determined their catalytic activity in the hydrogen peroxide decomposition reaction. Hydrogen peroxide decomposition on OOATsM and FTs of the metals studied follows the kinetic mechanisms of a reaction of the first order regardless of the central ion of the metal. Complexes with a central atom of iron are most active in decomposition of hydrogen peroxide. Catalytic activity of FTsFe exceeds that of FTsCo more than 10-fold. FTs are 10-fold greater than OOATsM in catalytic activity. Change from an acid to an alkali medium did not affect the kinetic mechanisms of the decomposition reaction but the reaction rate on both a carrier and on metal complexes is higher in an alkaline medium than in an acid medium. The affect of an alkaline medium on the hydrogen peroxide decomposition rate is greater for FTS complexes than for anthraquinone-cyanines. 5 references, 2 figures.

  3. Biomass to hydrogen via fast pyrolysis and catalytic steam reforming

    Energy Technology Data Exchange (ETDEWEB)

    Chornet, E.; Wang, D.; Montane, D. [National Renewable Energy Lab., Golden, CO (United States)] [and others

    1995-09-01

    Fast pyrolysis of biomass results in a pyrolytic oil which is a mixture of (a) carbohydrate-derived acids, aldehydes and polyols, (b) lignin-derived substituted phenolics, and (c) extractives-derived terpenoids and fatty acids. The conversion of this pyrolysis oil into H{sub 2} and CO{sub 2} is thermodynamically favored under appropriate steam reforming conditions. Our efforts have focused in understanding the catalysis of steam reforming which will lead to a successful process at reasonable steam/carbon ratios arid process severities. The experimental work, carried out at the laboratory and bench scale levels, has centered on the performance of Ni-based catalysts using model compounds as prototypes of the oxygenates present in the pyrolysis oil. Steam reforming of acetic acid, hydroxyacetaldehyde, furfural and syringol has been proven to proceed rapidly within a reasonable range of severities. Time-on-stream studies are now underway using a fixed bed barometric pressure reactor to ascertain the durability of the catalysts and thus substantiate the scientific and technical feasibility of the catalytic reforming option. Economic analyses are being carried out in parallel to determine the opportunity zones for the combined fast pyrolysis/steam reforming approach. A discussion on the current state of the project is presented.

  4. Techno-economics of carbon preserving butanol production using a combined fermentative and catalytic approach.

    Science.gov (United States)

    Nilsson, Robert; Bauer, Fredric; Mesfun, Sennai; Hulteberg, Christian; Lundgren, Joakim; Wännström, Sune; Rova, Ulrika; Berglund, Kris Arvid

    2014-06-01

    This paper presents a novel process for n-butanol production which combines a fermentation consuming carbon dioxide (succinic acid fermentation) with subsequent catalytic reduction steps to add hydrogen to form butanol. Process simulations in Aspen Plus have been the basis for the techno-economic analyses performed. The overall economy for the novel process cannot be justified, as production of succinic acid by fermentation is too costly. Though, succinic acid price is expected to drop drastically in a near future. By fully integrating the succinic acid fermentation with the catalytic conversion the need for costly recovery operations could be reduced. The hybrid process would need 22% less raw material than the butanol fermentation at a succinic acid fermentation yield of 0.7g/g substrate. Additionally, a carbon dioxide fixation of up to 13ktonnes could be achieved at a plant with an annual butanol production of 10ktonnes.

  5. Catalytic Hydrolysis of Ammonia Borane by Cobalt Nickel Nanoparticles Supported on Reduced Graphene Oxide for Hydrogen Generation

    Directory of Open Access Journals (Sweden)

    Yuwen Yang

    2014-01-01

    Full Text Available Well dispersed magnetically recyclable bimetallic CoNi nanoparticles (NPs supported on the reduced graphene oxide (RGO were synthesized by one-step in situ coreduction of aqueous solution of cobalt(II chloride, nickel (II chloride, and graphite oxide (GO with ammonia borane (AB as the reducing agent under ambient condition. The CoNi/RGO NPs exhibits excellent catalytic activity with a total turnover frequency (TOF value of 19.54 mol H2 mol catalyst−1 min−1 and a low activation energy value of 39.89 kJ mol−1 at room temperature. Additionally, the RGO supported CoNi NPs exhibit much higher catalytic activity than the monometallic and RGO-free CoNi counterparts. Moreover, the as-prepared catalysts exert satisfying durable stability and magnetically recyclability for the hydrolytic dehydrogenation of AB, which make the practical reusing application of the catalysts more convenient. The usage of the low-cost, easy-getting catalyst to realize the production of hydrogen under mild condition gives more confidence for the application of ammonia borane as a hydrogen storage material. Hence, this general method indicates that AB can be used as both a potential hydrogen storage material and an efficient reducing agent, and can be easily extended to facile preparation of other RGO-based metallic systems.

  6. Hydrogen production through biocatalyzed electrolysis

    OpenAIRE

    Rozendal, R.A.

    2007-01-01

    cum laude graduation (with distinction) To replace fossil fuels, society is currently considering alternative clean fuels for transportation. Hydrogen could be such a fuel. In theory, large amounts of renewable hydrogen can be produced from organic contaminants in wastewater. During his PhD research René Rozendal has developed a new technology for this purpose: biocatalyzed electrolysis. The innovative step of biocatalyzed electrolysis is the application of electrochemically active microorgan...

  7. Visbreaking based integrated process for bitumen upgrading and hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Sosa, C.; Gonzalez, M.F.; Carbognani, L.; Perez-Zurita, M.J.; Lopez-Linares, F.; Husein, M.; Moore, G.; Pereira, P. [Calgary Univ., AB (Canada). Alberta In Situ Centre For In Situ Energy, Schulich School Of Engineering

    2006-07-01

    New and cost effective upgrading schemes for distillates production and residue disposal are needed in order to recover Alberta's vast heavy oil and bitumen reserves. On average, heavy oils and bitumen contain 50 per cent (w/w) of components remaining after vacuum distillation. A new alternative for upgrading vacuum resids was proposed. The method involves the following 3 processing steps: production of modified, nearly unstable heavy molecules by mild thermal cracking known as visbreaking; adsorption of modified heavy molecules over inexpensive, tailor-designed porous sorbents or catalysts; and, production of hydrogen by low temperature catalytic steam gasification of the adsorbed molecules. This cost effective way of producing hydrogen is based on the selective segregation of a minimal fraction of the heaviest hydrocarbon molecules, those most instable, followed by their gasification at low temperature. This paper presented results on the combined processing as well as using both a model molecule and real feedstock from the Athabasca vacuum resids for the adsorption and hydrogen production steps. The study showed that this new process can obtain high rates of hydrogen production when a kaolin based solid formulation is used as both, adsorbent and catalysts, for these heavy molecules. It was concluded that this alternative method for producing hydrogen at upgrading sites in northern Alberta has potential for both installed and future up-graders to improve the quality of synthetic crude being produced. The hydrogen produced from the gasification of these heavy compounds could be used for both refining purposes or for in-situ reservoir upgrading. 27 refs., 3 figs.

  8. Fusion reactors for hydrogen production via electrolysis

    Science.gov (United States)

    Fillo, J. A.; Powell, J. R.; Steinberg, M.

    The decreasing availability of fossil fuels emphasizes the need to develop systems which will produce synthetic fuel to substitute for and supplement the natural supply. An important first step in the synthesis of liquid and gaseous fuels is the production of hydrogen. Thermonuclear fusion offers an inexhaustible source of energy for the production of hydrogen from water. Depending on design, electric generation efficiencies of 40 to 60% and hydrogen production efficiencies by high temperature electrolysis of 50 to 70% are projected for fusion reactors using high temperature blankets.

  9. Developments and constraints in fermentative hydrogen production

    NARCIS (Netherlands)

    Bartacek, J.; Zabranska, J.; Lens, P.N.L.

    2007-01-01

    Fermentative hydrogen production is a novel aspect of anaerobic digestion. The main advantage of hydrogen is that it is a clean and renewable energy source/carrier with high specific heat of combustion and no contribution to the Greenhouse effect, and can be used in many industrial applications. Thi

  10. Catalytic stepwise nitrate hydrogenation in batch-recycle fixed-bed reactors.

    Science.gov (United States)

    Pintar, Albin; Batista, Jurka

    2007-10-22

    Pd (1.0 wt.%)-Cu (0.3 wt.%) bimetallic and Pd (1.0 wt.%) monometallic catalysts were synthesized by means of incipient-wetness impregnation technique and deposited on alumina spheres (dp=1.7 mm). The prepared catalysts were tested at T=298 K and p(H2)=1.0 bar in the integrated process of catalytic liquid-phase hydrogenation of aqueous nitrate solutions, in which the denitration step was carried out consecutively in separate, single-flow fixed-bed reactor units operating in a batch-recycle mode. In the first reactor packed with a Pd-Cu bimetallic catalyst, nitrate ions were transformed to nitrites at pH 12.5 with a selectivity as high as 93%; the rest was found in the form of ammonium ions. Liquid-phase nitrite hydrogenation to nitrogen in the second reactor unit packed with a Pd monometallic catalyst was conducted at low pH values of 3.7 and 4.5, respectively. Although these values are well below the pHpzc of examined catalyst (6.1), which assured that the nitrite reduction was carried out over a positively charged catalyst surface, up to 15% (23% in the presence of 5.0 g/l NaCl in the solution) of initial nitrite content was converted to undesired ammonium ions. Since a negligible amount of these species (below 0.5mg/l) was produced at identical operating conditions over a powdered Pd/gamma-Al2O3 catalyst, it is believed that the enhanced production of ammonium ions observed in the second fixed-bed reactor is due to the build-up of pH gradients in liquid-filled pores of spherical catalyst particles. Both Pd-Cu bimetallic and Pd monometallic catalysts were chemically resistant in the investigated range of pH values.

  11. Research of Hydrogen Preparation with Catalytic Steam-Carbon Reaction Driven by Photo-Thermochemistry Process

    Directory of Open Access Journals (Sweden)

    Xiaoqing Zhang

    2013-01-01

    Full Text Available An experiment of hydrogen preparation from steam-carbon reaction catalyzed by K2CO3 was carried out at 700°C, which was driven by the solar reaction system simulated with Xenon lamp. It can be found that the rate of reaction with catalyst is 10 times more than that without catalyst. However, for the catalytic reaction, there is no obvious change for the rate of hydrogen generation with catalyst content range from 10% to 20%. Besides, the conversion efficiency of solar energy to chemical energy is more than 13.1% over that by photovoltaic-electrolysis route. An analysis to the mechanism of catalytic steam-carbon reaction with K2CO3 is given, and an explanation to the nonbalanced [H2]/[CO + 2CO2] is presented, which is a phenomenon usually observed in experiment.

  12. A new process for preparing dialdehyde by catalytic oxidation of cyclic olefins with aqueous hydrogen peroxide

    Institute of Scientific and Technical Information of China (English)

    YU, Hong-Kun; PANG, Zhen; HUANG, Zu-En; CAI, Rui-Fang

    2000-01-01

    A novel peroxo-nioboplosphate was synthesized for the first time and used as a catalyst in the oxidation reaction of cyclic olefins with aqueous hydrogen peroxide to prepare dialdehydes. The catalyst was characterized by elemental analysis,thermographic analyses, IR, UV/vis, 31P NMR and XPS ~ as [ π-C5H5N(CH2)i3CH3 ]2 [Nb406 (O2)2 (PO4)2] ·6H20 (PTNP). It showed high selectivity to glutaraldehyde in the catalytic oxidation of cyclopentene with aqueous hydrogen peroxide in ethanol.

  13. Catalytic hydrotreating of biomass liquefaction products to produce hydrocarbon fuels: Interim report

    Energy Technology Data Exchange (ETDEWEB)

    Elliott, D.C.; Baker, E.G.

    1986-03-01

    Research catalytic hydrotreatment of biomass liquefaction products to a gasoline has been technically demonstrated in a bench-scale continuous processing unit. This report describes the development of the chemistry needed for hydrotreatment of both high pressure and pyrolyzate biomass liquefaction products and outlines the important processing knowledge gained by the research. Catalyst identity is important in hydrotreatment of phenolics. Hydrogenation catalysts such as palladium, copper chromite, cobalt and nickel show activity with nickel being the most active. Major products include benzene, cyclohexane, and cyclohexanone. The hydrotreating catalysts cobalt-molybdenum, nickel-molybdenum and nickel-tungsten exhibit some activity when added to the reactor in the oxide form and show a great specificity for hydrodeoxygenation of phenol without saturation of the benzene product. The sulfide form of these catalysts is much more active than the oxide form and, in the case of the cobalt-molybdenum, much of the specificity for hydrodeoxygenation is retained. Substitution on the phenolic ring has only marginal effects on the hydrotreating reaction. However, the methoxy (OCH/sub 3/) substituent on the phenol ring is thermally unstable relative to other phenolics tested. The pyrolysis products dominate the product distribution when cobalt-molybdenum is used as the hydrotreating catalyst for methoxyphenol. The product from catalytic hydrotreatment of high-pressure biomass liquefaction products confirms the model compounds studies. Catalytic processing at 350 to 400/sup 0/C and 2000 psig with the sulfided cobalt-molybdenum or nickel-molybdenum catalyst produced a gasoline-like product composed of cyclic and aromatic compounds. Oxygen contents in products were in the range of 0 to 0.7 wt % and hydrogen to carbon atomic ratios ranged from 1.5 to 2.0. 46 refs., 10 figs., 21 tabs.

  14. Hydrogen production from biomass over steam gasification

    Energy Technology Data Exchange (ETDEWEB)

    Rauch, R.; Potetz, A.; Hofbauer, H. [Vienna Univ. of Technology (Austria). Inst. of Chemical Engineering; Weber, G. [Bioenergy 2020+, Guessing (Austria)

    2010-12-30

    Renewable hydrogen is one option for a clean energy carrier in the future. There were several research programs in the past, to produce hydrogen on a renewable basis by electrolysis, direct conversion of water or by gasification of biomass. None of these options were developed to a stage, that they could be used on a commercial basis. At the moment almost all hydrogen is produced from fossil fuels and one main consumer of hydrogen are refineries. So a good option to demonstrate the production of renewable hydrogen and bring it later into the market is over refineries. The most economic option to produce renewable hydrogen at the moment is over gasification of biomass. In Austria an indirect gasification system was developed and is demonstrated in Guessing, Austria. The biomass CHP Guessing uses the allothermal steam dual fluidised bed gasifier and produces a high grade product gas, which is used at the moment for the CHP in a gas engine. As there is no nitrogen in the product gas and high hydrogen content, this gas can be also used as synthesis gas or for production of hydrogen. The main aim of this paper is to present the experimental and simulation work to convert biomass into renewable hydrogen. The product gas of the indirect gasification system is mainly hydrogen, carbon monoxide, carbon dioxide and methane. Within the ERA-Net project ''OptiBtLGas'' the reforming of methane and the CO-shift reaction was investigated to convert all hydrocarbons and carbon monoxide to hydrogen. On basis of the experimental results the mass- and energy balances of a commercial 100 MW fuel input plant was done. Here 3 different cases of complexity of the overall plant were simulated. The first case was without reforming and CO-shift, only by hydrogen separation. The second case was by including steam - reforming and afterwards separation of hydrogen. The third case includes hydrocarbon reforming, CO-shift and hydrogen separation. In all cases the off-gases (CO

  15. Fermentative hydrogen production at high sulfate concentration

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Chin-Chao [Environmental Resources Laboratory, Department of Landscape Architecture, Chungchou Institute of Technology, Changhwa 51022 (China); Chen, Hong-Pin; Wu, Jou-Hsien; Lin, Chiu-Yue [BioHydrogen Laboratory, Department of Water Resource Engineering, Feng Chia University, P.O. Box 25-123, Taichung 40724 (China)

    2008-03-15

    The hydraulic retention time (HRT) effects on fermentative hydrogen production from sucrose at high sulfate concentration of 3 g-SO{sub 4}{sup 2-}/l were studied using enriched mixed-microflora in a continuously fed reactor. The tested HRTs and organic loading rate ranged from 10 to 2 h and 48 to 240 g-COD/l-day, respectively, and the operating pH was 5.5. The experimental results indicate that hydrogen production could not be inhibited under high sulfate concentration and the efficiency was HRT-dependent with a short HRT of 4 h efficiently enhanced hydrogen production. At this HRT the biogas production rate and hydrogen gas content peaked with the hydrogen yield, hydrogen production rate and specific hydrogen production rate of 4.70 mol-H{sub 2}/mol-sucrose, 874 mmol-H{sub 2}/l-day and 432 mmol-H{sub 2}/g-VSS-day, respectively. These values were 50%, 80% and 300%, respectively, higher than those reported for 12 h HRT at the same sulfate concentration. The metabolite concentration fractions were butyrate 77.3%, acetate 15.6%, ethanol 4.4% and propionate 2.0% and changed to 55%, 27.3%, 11.2% and 6.5%, respectively, at HRT 2 h. Therefore, intimate HRT control is important to obtain efficient hydrogen production. Based on a biological growth comparison, pH 5.5 was considered to be the optimal value for operating a hydrogen-producing fermenter fed on sulfate-rich substrate. (author)

  16. State of the art on hydrogen passive auto-catalytic recombiner (european union Parsoar project)

    Energy Technology Data Exchange (ETDEWEB)

    Arnould, F.; Bachellerie, E. [Technicatome, 13 - Aix en Provence (France); Auglaire, M. [Tractebel Energy Engineering, Brussels (Belgium); Boeck, B. de [Association Vincotte Nuclear, Brussels (Belgium); Braillard, O. [CEA Cadarache, 13 - Saint Paul lez Durance (France); Eckardt, B. [Siemens AG, Offenbach am Main (Germany); Ferroni, F. [Electrowatt Engineering Limited, Zurich (Switzerland); Moffett, R. [Atomic Energy Canada Limited, Pinawa (Canada); Van Goethem, G. [European Commission, Brussels (Belgium)

    2001-07-01

    This paper presents an overview of the European Union PARSOAR project, which consists in carrying out a state of the art on hydrogen passive auto-catalytic recombiner (PAR) and a handbook guide for implementing these devices in nuclear power plants. This work is performed in the area ''Operational Safety of Existing Installations'' of the key action ''Nuclear Fission'' of the fifth Euratom Framework Programme (1998-2002). (author)

  17. Production of hydrogen by superadiabatic decomposition of hydrogen sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Slimane, R.B.; Lau, F.S.; Dihu, R. [Gas Technology Inst., Des Plaines, IL (United States); Bingue, J.P.; Saveliev, A.V.; Fridman, A.A.; Kennedy, L.A. [Illinois Univ., Chicago, IL (United States)

    2002-07-01

    It is expected that hydrogen will become the fuel of choice for advanced technologies. Hydrogen is currently used as feedstock in the synthesis of ammonia and methanol, in the desulfurization and hydrocracking at oil refineries, and in the upgrading of hydrocarbon resources such as heavy oil and coal. Hydrogen sulfide (H{sub 2}S) is regarded as a mineral from which both hydrogen and sulfur can be extracted. Since there are large amounts of H{sub 2}S available worldwide, significant research has gone into the development of converting hydrogen sulfide into hydrogen through thermal decomposition. The high temperature required for the reaction, however, makes the approach impractical. This paper presents results of a study using a new approach to overcome the limitations of thermal decomposition. In this newly developed process, operation at very high temperatures is possible and economical through oxidation of part of the H{sub 2}S to provide the energy needed for the decomposition reaction. Partial oxidation is carried out in the presence of an inert, porous, high-capacity medium and the heat exchange results in flame temperatures that exceed the adiabatic flame temperature of the gas mixture. This process is less stringent than the Claus process because of the required feed gas conditioning. SO{sub 2} emissions inevitably form because part of the H{sub 2}S is oxidized to generate heat. However, SO{sub 2} is not expected to form to a significant degree. It was concluded that the product/byproduct separation schemes need to be examined further to have a better idea regarding the cost of hydrogen production from this process. 6 refs., 5 figs.

  18. Photobiological production of hydrogen using cyanobacteria

    Energy Technology Data Exchange (ETDEWEB)

    Borthakur, D.; McKinley, K.R.; Bylina, E.J. [Univ. of Hawaii, Honolulu, HI (United States)

    1995-09-01

    Cyanobacteria are capable of generating hydrogen using sunlight and water. In both Spirulina and Anabaena, there is a soluble reversible hydrogenase that is involved in hydrogen evolution under anaerobic conditions in the dark. In addition, the nitrogen-fixing cyanobacterium Anabaena produces hydrogen as a by-product of nitrogen fixation. Most of this hydrogen is recaptured by a membrane-bound uptake hydrogenase present in Anabaena cells. Experiments have continued to develop a gene transfer system in Spirulina in preparation for improved hydrogen production via genetic manipulation of the reversible hydrogenase. We have identified and characterized four restriction enzymes in Spirulina and cloned the genes for two methylases that protect their own DNA from cleavage by restriction enzymes. We have also cloned and sequenced parts of hupB and hupM genes involved in the synthesis of uptake hydrogenase in Anabaena. Successful cloning of these hup genes represents an important and necessary step in our project because this will enable us to construct Anabaena strains with enhanced hydrogen production ability by disrupting the hup genes involved in hydrogen uptake. We are also setting up a bio-reactor to determine the amount of hydrogen released by different Spirulina and Anabaena strains under different physiological conditions.

  19. Biological hydrogen production from industrial wastewaters

    Energy Technology Data Exchange (ETDEWEB)

    Peixoto, Guilherme; Pantoja Filho, Jorge Luis Rodrigues; Zaiat, Marcelo [Universidade de Sao Paulo (EESC/USP), Sao Carlos, SP (Brazil). School of Engineering. Dept. Hydraulics and Sanitation], Email: peixoto@sc.usp.br

    2010-07-01

    This research evaluates the potential for producing hydrogen in anaerobic reactors using industrial wastewaters (glycerol from bio diesel production, wastewater from the parboilization of rice, and vinasse from ethanol production). In a complementary experiment the soluble products formed during hydrogen production were evaluated for methane generation. The assays were performed in batch reactors with 2 liters volume, and sucrose was used as a control substrate. The acidogenic inoculum was taken from a packed-bed reactor used to produce hydrogen from a sucrose-based synthetic substrate. The methanogenic inoculum was taken from an upflow anaerobic sludge blanket reactor treating poultry slaughterhouse wastewater. Hydrogen was produced from rice parboilization wastewater (24.27 ml H{sub 2} g{sup -1} COD) vinasse (22.75 ml H{sub 2} g{sup -1} COD) and sucrose (25.60 ml H{sub 2} g{sup -1} COD), while glycerol only showed potential for methane generation. (author)

  20. Liquid-Phase Catalytic Transfer Hydrogenation of Furfural over Homogeneous Lewis Acid-Ru/C Catalysts.

    Science.gov (United States)

    Panagiotopoulou, Paraskevi; Martin, Nickolas; Vlachos, Dionisios G

    2015-06-22

    The catalytic performance of homogeneous Lewis acid catalysts and their interaction with Ru/C catalyst are studied in the catalytic transfer hydrogenation of furfural by using 2-propanol as a solvent and hydrogen donor. We find that Lewis acid catalysts hydrogenate the furfural to furfuryl alcohol, which is then etherified with 2-propanol. The catalytic activity is correlated with an empirical scale of Lewis acid strength and exhibits a volcano behavior. Lanthanides are the most active, with DyCl3 giving complete furfural conversion and a 97 % yield of furfuryl alcohol at 180 °C after 3 h. The combination of Lewis acid and Ru/C catalysts results in synergy for the stronger Lewis acid catalysts, with a significant increase in the furfural conversion and methyl furan yield. Optimum results are obtained by using Ru/C combined with VCl3 , AlCl3 , SnCl4 , YbCl3 , and RuCl3 . Our results indicate that the combination of Lewis acid/metal catalysts is a general strategy for performing tandem reactions in the upgrade of furans.

  1. Thermocatalytic CO2-Free Production of Hydrogen from Hydrocarbon Fuels

    Energy Technology Data Exchange (ETDEWEB)

    University of Central Florida

    2004-01-30

    The main objective of this project is the development of an economically viable thermocatalytic process for production of hydrogen and carbon from natural gas or other hydrocarbon fuels with minimal environmental impact. The three major technical goals of this project are: (1) to accomplish efficient production of hydrogen and carbon via sustainable catalytic decomposition of methane or other hydrocarbons using inexpensive and durable carbon catalysts, (2) to obviate the concurrent production of CO/CO{sub 2} byproducts and drastically reduce CO{sub 2} emissions from the process, and (3) to produce valuable carbon products in order to reduce the cost of hydrogen production The important feature of the process is that the reaction is catalyzed by carbon particulates produced in the process, so no external catalyst is required (except for the start-up operation). This results in the following advantages: (1) no CO/CO{sub 2} byproducts are generated during hydrocarbon decomposition stage, (2) no expensive catalysts are used in the process, (3) several valuable forms of carbon can be produced in the process depending on the process conditions (e.g., turbostratic carbon, pyrolytic graphite, spherical carbon particles, carbon filaments etc.), and (4) CO{sub 2} emissions could be drastically reduced (compared to conventional processes).

  2. Photo-biotechnological hydrogen production with microalgae

    Energy Technology Data Exchange (ETDEWEB)

    Lehr, F.; Posten, C. [Inst. fuer Bio- und Lebensmitteltechnik, Univ. Karlsruhe (Germany); Renz, A.; Schaub, G. [Engler-Bunte-Inst., Univ. Karlsruhe (Germany)

    2008-07-01

    Some types of unicellular green algae have evolved the ability to use solar energy to produce hydrogen by splitting water. Compared to photosynthesis with terrestrial plants, microalgal hydrogen production exhibits higher photo conversion efficiencies, very low water demands, and no competition with agriculture for arable land use. The overall process includes microalgae growth by photosynthesis and subsequent hydrogen production. The main challenge in process development is the design of photo bioreactors with minimum energy demand for mixing and liquid handling and maximum overall efficiency. In an ongoing research project, process engineering fundamentals are presently being investigated in order to allow more accurate process design and cost estimates. (orig.)

  3. Hydrogen production using ammonia borane

    Science.gov (United States)

    Hamilton, Charles W; Baker, R. Thomas; Semelsberger, Troy A; Shrestha, Roshan P

    2013-12-24

    Hydrogen ("H.sub.2") is produced when ammonia borane reacts with a catalyst complex of the formula L.sub.nM-X wherein M is a base metal such as iron, X is an anionic nitrogen- or phosphorus-based ligand or hydride, and L is a neutral ancillary ligand that is a neutral monodentate or polydentate ligand.

  4. Fermentative hydrogen production by diverse microflora

    Energy Technology Data Exchange (ETDEWEB)

    Baghchehsaraee, B.; Nakhla, G.; Karamanev, D.; Margaritis, A. [Dept. of Chemical and Biochemical Engineering, Univ. of Western Ontario, London, Ontario (Canada)

    2009-07-01

    'Full text': In this study of hydrogen production with activated sludge, a diverse bacterial source has been investigated and compared to microflora from anaerobic digester sludge, which is less diverse. Batch experiments were conducted at mesophilic (37 {sup o}C) and thermophilic (55 {sup o}C) temperatures. The hydrogen production yields with activated sludge at 37 {sup o}C and 55 {sup o}C were 0.25 and 0.93 mol H{sub 2}/mol glucose, respectively. The maximum hydrogen production rates with activated sludge in both temperatures were 4.2 mL/h. Anaerobic digester sludge showed higher hydrogen production yields and rates at both mesophilic and thermophilic temperatures. The results of repeated batch experiments with activated sludge showed an increase in the hydrogen production during the consecutive batches. However, hydrogen production was not stable along the repeated batches. The observed instability was due to the formation of lactic acid and ethanol. (author)

  5. Catalytic abatement of nitrous oxide from nitric and production

    NARCIS (Netherlands)

    Oonk, J.

    1998-01-01

    Nitric acid production is identified as a main source of nitrous oxide. Options for emission reduction however are not available. TNO and Hydro Agri studied the technological and economic feasibility of catalytic decomposition of nitrous oxide in nitric acid tail-gases. Although in literature promis

  6. Catalytic enantioselective amination of alcohols by the use of borrowing hydrogen methodology: cooperative catalysis by iridium and a chiral phosphoric acid.

    Science.gov (United States)

    Zhang, Yao; Lim, Ching-Si; Sim, Derek Sui Boon; Pan, Hui-Jie; Zhao, Yu

    2014-01-27

    The catalytic asymmetric reduction of ketimines has been explored extensively for the synthesis of chiral amines, with reductants ranging from Hantzsch esters, silanes, and formic acid to H2 gas. Alternatively, the amination of alcohols by the use of borrowing hydrogen methodology has proven a highly atom economical and green method for the production of amines without an external reductant, as the alcohol substrate serves as the H2 donor. A catalytic enantioselective variant of this process for the synthesis of chiral amines, however, was not known. We have examined various transition-metal complexes supported by chiral ligands known for asymmetric hydrogenation reactions, in combination with chiral Brønsted acids, which proved essential for the formation of the imine intermediate and the transfer-hydrogenation step. Our studies led to an asymmetric amination of alcohols to provide access to a wide range of chiral amines with good to excellent enantioselectivity.

  7. Carbon Dioxide-Free Hydrogen Production with Integrated Hydrogen Separation and Storage.

    Science.gov (United States)

    Dürr, Stefan; Müller, Michael; Jorschick, Holger; Helmin, Marta; Bösmann, Andreas; Palkovits, Regina; Wasserscheid, Peter

    2017-01-10

    An integration of CO2 -free hydrogen generation through methane decomposition coupled with hydrogen/methane separation and chemical hydrogen storage through liquid organic hydrogen carrier (LOHC) systems is demonstrated. A potential, very interesting application is the upgrading of stranded gas, for example, gas from a remote gas field or associated gas from off-shore oil drilling. Stranded gas can be effectively converted in a catalytic process by methane decomposition into solid carbon and a hydrogen/methane mixture that can be directly fed to a hydrogenation unit to load a LOHC with hydrogen. This allows for a straight-forward separation of hydrogen from CH4 and conversion of hydrogen to a hydrogen-rich LOHC material. Both, the hydrogen-rich LOHC material and the generated carbon on metal can easily be transported to destinations of further industrial use by established transport systems, like ships or trucks.

  8. Recent Developments in Biological Hydrogen Production Processes

    Directory of Open Access Journals (Sweden)

    DEBABRATA DAS

    2008-07-01

    Full Text Available Biohydrogen production technology can utilize renewable energy sources like biomass for the generation of hydrogen, the cleanest form of energy for the use of mankind. However, major constraints to the commercialization of these processes include lower hydrogen yields and rates of hydrogen production. To overcome these bottlenecks intensive research work has already been carried out on the advancement of these processes such as the development of genetically modified microorganisms, the improvement of the bioreactor design, molecular engineering of the key enzyme hydrogenases, the development of two stage processes, etc. The present paper explores the recent advancements that have been made till date and also presents the state of the art in molecular strategies to improve the hydrogen production.

  9. Substrate-mediated enhanced activity of Ru nanoparticles in catalytic hydrogenation of benzene

    KAUST Repository

    Liu, Xin

    2012-01-01

    The impact of carbon substrate-Ru nanoparticle interactions on benzene and hydrogen adsorption that is directly related to the performance in catalytic hydrogenation of benzene has been investigated by first-principles based calculations. The stability of Ru 13 nanoparticles is enhanced by the defective graphene substrate due to the hybridization between the dsp states of the Ru 13 particle with the sp 2 dangling bonds at the defect sites. The local curvature formed at the interface will also raise the Ru atomic diffusion barrier, and prohibit the particle sintering. The strong interfacial interaction results in the shift of averaged d-band center of the deposited Ru nanoparticle, from -1.41 eV for a freestanding Ru 13 particle, to -1.17 eV for the Ru/Graphene composites, and to -1.54 eV on mesocellular foam carbon. Accordingly, the adsorption energies of benzene are increased from -2.53 eV for the Ru/mesocellular foam carbon composites, to -2.62 eV on freestanding Ru 13 particles, to -2.74 eV on Ru/graphene composites. A similar change in hydrogen adsorption is also observed, and all these can be correlated to the shift of the d-band center of the nanoparticle. Thus, Ru nanoparticles graphene composites are expected to exhibit both high stability and superior catalytic performance in hydrogenation of arenes. © 2012 The Royal Society of Chemistry.

  10. Extremophile mediated hydrogen production for hydrogenation of substrates in aqueous media

    Science.gov (United States)

    Anjom, Mouzhgun

    Catalytic hydrogenation reactions are pervasive throughout our economy, from production of margarine as food, liquid fuels for transportation and chiral drugs such as L-DOPA. H2 production from non-fossil fuel feedstocks is highly desirable for transition to the "Hydrogen Economy". Also, the rates of hydrogenation reactions that involve a substrate, H 2 gas and a catalyst are often limited by the solubility of H2 in solvent. The present research thus envisioned designing water-soluble catalysts that could effectively utilize biologically produced H2 in a coupled system to hydrogenate substrates in homogeneous mode (two-phase system). Biological production of H2 as an end product or byproduct of the metabolism of organisms that operate under strict anaerobic conditions has been proposed. However, contrary to what was previously observed, Thermotoga neapolitana, belonging to the order of Thermotogales efficiently produces H2 gas under microaerobic conditions (Van Ooteghem et al. 2004). For H2 production by T. neapolitana in the bacterial growth medium (DSM 5068) at an optimum temperature of 70 C, our results in batch mode show that: (1) H2 was produced from glucose though with 16% efficiency, the rest goes to biomass production, (2) H2 gas was produced even when the cultures were inoculated under microaerobic conditions (up to 8% (v/v) O2) suggesting a protective mechanism for one or more [Fe-Fe] hydrogenases in T. neapolitana, (3) H2 production was pH dependent but addition of simple, non-toxic physiological buffering additives such as Methylene succinic acid increased H2 production and (4) H2 production rate varied linearly in the 100--6800 kPa pressure range. We then screened various water-soluble metal catalysts in batch mode and selected the RhCl3.3H2O/TPPTS (TPPTS is a water-soluble ligand) system that achieved 86% hydrogenation of Methylene succinic acid (an olefin) in an aqueous medium pressurized with preformed H2. When water was replaced with the DSM 5068

  11. Study on the production of alternative fuels by carbon dioxide hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Sim, Kyu Sung; Han, Sang Do; Kim, Jong Won; Kim, Youn Soon; Seo, Ji Mi [Korea Inst. of Energy Research, Taejon (Korea, Republic of)

    1995-12-01

    The technologies of the fuel production from carbon dioxide by catalytic hydrogenation were surveyed. For the catalytic hydrogenation we made the lab-scale reaction apparatus and carried out some experiments with various catalysts like CuO/ZnO/Al{sub 2}O{sub 3}, Raney nickel and other commercial catalysts. In this year, the third year of the project, the experiments to find optimum catalysts and obtain the good conditions of carbon dioxide were performed followed by second year. And also the processes of the methanol synthesis was investigated simultaneously. (author). 58 refs., 58 figs., 28 tabs.

  12. Enhancing fermentative hydrogen production from sucrose.

    Science.gov (United States)

    Perera, Karnayakage Rasika J; Nirmalakhandan, Nagamany

    2010-12-01

    This study evaluated the hypothesis that fermentative hydrogen production from organic-rich feedstock could be enhanced by supplementing with waste materials such as cattle manure that could provide nutritional needs, buffering capacity, and native hydrogen-producing organisms. This hypothesis was tested in batch reactors fed with sucrose blended with cattle manure run at 25 degrees C without any nutrient supplements, pH adjustments, buffering, or gas-sparging. Hydrogen production rates in these reactors ranged 16-30 mL H(2)/g DeltaCOD-day, while hydrogen content in the biogases ranged 50-59%. Compared to literature studies conducted at higher temperatures, hydrogen yields found in this study at 25 degrees C were higher in the range of 3.8-4.7 mol H(2)/mol sucrose added, with higher positive net energy yields (>14 kJ/L). This study demonstrated that cattle manure as a supplement could not only provide hydrogen-producing seed, nutritional needs, and buffering capacity, but also increase hydrogen yield by approximately 10%, improving the economic viability of fermentative biohydrogen production from sugary wastes.

  13. Wax: A benign hydrogen-storage material that rapidly releases H2-rich gases through microwave-assisted catalytic decomposition.

    Science.gov (United States)

    Gonzalez-Cortes, S; Slocombe, D R; Xiao, T; Aldawsari, A; Yao, B; Kuznetsov, V L; Liberti, E; Kirkland, A I; Alkinani, M S; Al-Megren, H A; Thomas, J M; Edwards, P P

    2016-10-19

    Hydrogen is often described as the fuel of the future, especially for application in hydrogen powered fuel-cell vehicles (HFCV's). However, its widespread implementation in this role has been thwarted by the lack of a lightweight, safe, on-board hydrogen storage material. Here we show that benign, readily-available hydrocarbon wax is capable of rapidly releasing large amounts of hydrogen through microwave-assisted catalytic decomposition. This discovery offers a new material and system for safe and efficient hydrogen storage and could facilitate its application in a HFCV. Importantly, hydrogen storage materials made of wax can be manufactured through completely sustainable processes utilizing biomass or other renewable feedstocks.

  14. Hydrogen Peroxide as a Sustainable Energy Carrier: Electrocatalytic Production of Hydrogen Peroxide and the Fuel Cell

    OpenAIRE

    Fukuzumi, Shunichi; Yamada, Yusuke; Karlin, Kenneth D.

    2012-01-01

    This review describes homogeneous and heterogeneous catalytic reduction of dioxygen with metal complexes focusing on the catalytic two-electron reduction of dioxygen to produce hydrogen peroxide. Whether two-electron reduction of dioxygen to produce hydrogen peroxide or four-electron O2-reduction to produce water occurs depends on the types of metals and ligands that are utilized. Those factors controlling the two processes are discussed in terms of metal-oxygen intermediates involved in the ...

  15. Enhanced Hydrogen Production Integrated with CO2 Separation in a Single-Stage Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Shwetha Ramkumar; Mahesh Iyer; Danny Wong; Himanshu Gupta; Bartev Sakadjian; Liang-Lhih Fan

    2008-09-30

    High purity hydrogen is commercially produced from syngas by the Water Gas Shift Reaction (WGSR) in high and low temperature shift reactors using iron oxide and copper catalysts respectively. However, the WGSR is thermodynamically limited at high temperatures towards hydrogen production necessitating excess steam addition and catalytic operation. In the calcium looping process, the equilibrium limited WGSR is driven forward by the incessant removal of CO{sub 2} by-product through the carbonation of calcium oxide. At high pressures, this process obviates the need for a catalyst and excess steam requirement, thereby removing the costs related to the procurement and deactivation of the catalyst and steam generation. Thermodynamic analysis for the combined WGS and carbonation reaction was conducted. The combined WGS and carbonation reaction was investigated at varying pressures, temperatures and S/C ratios using a bench scale reactor system. It was found that the purity of hydrogen increases with the increase in pressure and at a pressure of 300 psig, almost 100% hydrogen is produced. It was also found that at high pressures, high purity hydrogen can be produced using stoichiometric quantities of steam. On comparing the catalytic and non catalytic modes of operation in the presence of calcium oxide, it was found that there was no difference in the purity of hydrogen produced at elevated pressures. Multicyclic reaction and regeneration experiments were also conducted and it was found that the purity of hydrogen remains almost constant after a few cycles.

  16. Spectroelectrochemical analysis of the mechanism of (photo)electrochemical hydrogen evolution at a catalytic interface

    Science.gov (United States)

    Pastor, Ernest; Le Formal, Florian; Mayer, Matthew T.; Tilley, S. David; Francàs, Laia; Mesa, Camilo A.; Grätzel, Michael; Durrant, James R.

    2017-02-01

    Multi-electron heterogeneous catalysis is a pivotal element in the (photo)electrochemical generation of solar fuels. However, mechanistic studies of these systems are difficult to elucidate by means of electrochemical methods alone. Here we report a spectroelectrochemical analysis of hydrogen evolution on ruthenium oxide employed as an electrocatalyst and as part of a cuprous oxide-based photocathode. We use optical absorbance spectroscopy to quantify the densities of reduced ruthenium oxide species, and correlate these with current densities resulting from proton reduction. This enables us to compare directly the catalytic function of dark and light electrodes. We find that hydrogen evolution is second order in the density of active, doubly reduced species independent of whether these are generated by applied potential or light irradiation. Our observation of a second order rate law allows us to distinguish between the most common reaction paths and propose a mechanism involving the homolytic reductive elimination of hydrogen.

  17. Spectroelectrochemical analysis of the mechanism of (photo)electrochemical hydrogen evolution at a catalytic interface

    Science.gov (United States)

    Pastor, Ernest; Le Formal, Florian; Mayer, Matthew T.; Tilley, S. David; Francàs, Laia; Mesa, Camilo A.; Grätzel, Michael; Durrant, James R.

    2017-01-01

    Multi-electron heterogeneous catalysis is a pivotal element in the (photo)electrochemical generation of solar fuels. However, mechanistic studies of these systems are difficult to elucidate by means of electrochemical methods alone. Here we report a spectroelectrochemical analysis of hydrogen evolution on ruthenium oxide employed as an electrocatalyst and as part of a cuprous oxide-based photocathode. We use optical absorbance spectroscopy to quantify the densities of reduced ruthenium oxide species, and correlate these with current densities resulting from proton reduction. This enables us to compare directly the catalytic function of dark and light electrodes. We find that hydrogen evolution is second order in the density of active, doubly reduced species independent of whether these are generated by applied potential or light irradiation. Our observation of a second order rate law allows us to distinguish between the most common reaction paths and propose a mechanism involving the homolytic reductive elimination of hydrogen. PMID:28233785

  18. A compact process for the treatment of olive mill wastewater by combining wet hydrogen peroxide catalytic oxidation and biological techniques.

    Science.gov (United States)

    Azabou, Samia; Najjar, Wahiba; Bouaziz, Mohamed; Ghorbel, Abdelhamid; Sayadi, Sami

    2010-11-15

    A system based on combined actions of catalytic wet oxidation and microbial technologies for the treatment of highly polluted OMW containing polyphenols was studied. The wet hydrogen peroxide catalytic oxidation (WHPCO) process has been investigated in the semi-batch mode at atmospheric pressure, using aluminium-iron-pillared inter layer clay ((Al-Fe)PILC), under two different catalytic processes: ((Al-Fe)PILC/H(2)O(2)/ultraviolet radiations) at 25°C and ((Al-Fe)PILC/H(2)O(2)) at 50°C. The results show that raw OMW was resistant to the photocatalytic process. However ((Al-Fe)PILC/H(2)O(2)), system operating at 50°C reduced considerably the COD, colour and total phenolic contents, and thus decreased the inhibition of the marine photobacteria Vibrio fischeri luminescence by 70%. This study also examined the feasibility of coupling WHPCO and anaerobic digestion treatment. Biomethanisation experiments performed with raw OMW or pre-treated OMW proved that pre-treatments with ((Al-Fe)PILC/H(2)O(2)) system, for more than 2 h, resulted in higher methane production. Both untreated OMW as well as 2-h pre-treated OMW revealed as toxic to anaerobic bacteria.

  19. Recent review of thermochemical hydrogen production

    Science.gov (United States)

    Beghi, G. E.

    A survey is presented on the development to date of thermochemical water decomposition methods for the production of hydrogen. It is shown that: (1) both the technological feasibility of thermochemical processes and their competitiveness with water electrolysis have been demonstrated; (2) the scaling up of thermochemical methods to industrial production levels may proceed with existing technology; (3) the slowing down of programs concerned with the development of high temperature nuclear reactors could delay the scaling up of thermochemical hydrogen production to industrial levels; (4) this delay could, however, increase interest in such water decomposition processes as those employing photoreactions; and (5) the efficiency of thermochemical hydrogen production is highest in the case of systems with dedicated heat sources rated above 1000 MWth.

  20. Microbial consortia for hydrogen production enhancement.

    Science.gov (United States)

    Rajhi, Haifa; Díaz, Emiliano E; Rojas, Patricia; Sanz, José L

    2013-07-01

    Ten efficient hydrogen-producing strains affiliated to the Clostridium genus were used to develop consortia for hydrogen production. In order to determine their saccharolytic and proteolytic activities, glucose and meat extract were tested as fermentation substrates, and the best hydrogen-producing strains were selected. The C. roseum H5 (glucose-consuming) and C. butyricum R4 (protein-degrading) co-culture was the best hydrogen-producing co-culture. The end-fermentation products for the axenic cultures and co-cultures were analyzed. In all cases, organic acids, mainly butyrate and acetate, were produced lowering the pH and thus inhibiting further hydrogen production. In order to replace the need for reducing agents for the anaerobic growth of clostridia, a microbial consortium including Clostridium spp. and an oxygen-consuming microorganism able to form dense granules (Streptomyces sp.) was created. Increased yields of hydrogen were achieved. The effect of adding a butyrate-degrading bacteria and an acetate-consuming archaea to the consortia was also studied.

  1. Continuous hydrogen production from starch by fermentation

    Energy Technology Data Exchange (ETDEWEB)

    Yasuda, Keigo; Tanisho, Shigeharu [Yokohama National Univ. (Japan)

    2010-07-01

    This study was investigated the effect of hydraulic retention time (HRT) on hydrogen production rate, hydrogen yield and the production rate of volatile fatty acid. The experiment was performed in a continuous stirred tank reactor (CSTR) with a working volume of 1 L by using a Clostridium sp. The temperature of the CSTR was regulated 37 C. The pH was controlled 6.0 by the addition of 3 M of NaOH solution. Starch was used as the carbon source with the concentration of 30 g L{sup -1}. Hydrogen production rate increased from 0.9 L-H{sub 2} L-culture{sup -1} h{sup -1} to 3.2 L-H{sub 2} L-culture{sup -1} h{sup -1} along with the decrease of HRT from 9 h to 1.5 h. Hydrogen yield decreased at low HRT. The major volatile fatty acids are acetic acid, butyric acid and lactic acid. The production rates of acetic acid and butyric acid increased along with the decrease of HRT. On the other hand, the rate of lactic acid was low at high HRT while it increased at HRT 1.5 h. The increase of the production rate of lactic acid suggested one of the reasons that hydrogen yield decreased. (orig.)

  2. Onboard Plasmatron Hydrogen Production for Improved Vehicles

    Energy Technology Data Exchange (ETDEWEB)

    Daniel R. Cohn; Leslie Bromberg; Kamal Hadidi

    2005-12-31

    A plasmatron fuel reformer has been developed for onboard hydrogen generation for vehicular applications. These applications include hydrogen addition to spark-ignition internal combustion engines, NOx trap and diesel particulate filter (DPF) regeneration, and emissions reduction from spark ignition internal combustion engines First, a thermal plasmatron fuel reformer was developed. This plasmatron used an electric arc with relatively high power to reform fuels such as gasoline, diesel and biofuels at an oxygen to carbon ratio close to 1. The draw back of this device was that it has a high electric consumption and limited electrode lifetime due to the high temperature electric arc. A second generation plasmatron fuel reformer was developed. It used a low-current high-voltage electric discharge with a completely new electrode continuation. This design uses two cylindrical electrodes with a rotating discharge that produced low temperature volumetric cold plasma., The lifetime of the electrodes was no longer an issue and the device was tested on several fuels such as gasoline, diesel, and biofuels at different flow rates and different oxygen to carbon ratios. Hydrogen concentration and yields were measured for both the thermal and non-thermal plasmatron reformers for homogeneous (non-catalytic) and catalytic reforming of several fuels. The technology was licensed to an industrial auto part supplier (ArvinMeritor) and is being implemented for some of the applications listed above. The Plasmatron reformer has been successfully tested on a bus for NOx trap regeneration. The successful development of the plasmatron reformer and its implementation in commercial applications including transportation will bring several benefits to the nation. These benefits include the reduction of NOx emissions, improving engine efficiency and reducing the nation's oil consumption. The objective of this program has been to develop attractive applications of plasmatron fuel reformer

  3. Marrying gas power and hydrogen energy: A catalytic system for combining methane conversion and hydrogen generation

    NARCIS (Netherlands)

    Beckers, J.; Gaudillère, C.; Farrusseng, D.; Rothenberg, G.

    2009-01-01

    Ceria-based catalysts are good candidates for integrating methane combustion and hydrogen generation. These new, tuneable catalysts are easily prepared. They are robust inorganic crystalline materials, and perform well at the 400 °C-550 °C range, in some cases even without precious metals. This make

  4. Fermentative hydrogen production by diverse microflora

    Energy Technology Data Exchange (ETDEWEB)

    Baghchehsaraee, Bita; Nakhla, George; Karamanev, Dimitre; Margaritis, Argyrios [Department of Chemical and Biochemical Engineering, The University of Western Ontario, London, Ontario N6A 5B9 (Canada)

    2010-05-15

    In this study, hydrogen production with activated sludge, a diverse bacterial source has been investigated and compared to microflora from anaerobic digester sludge, which is less diverse. Batch experiments were conducted at mesophilic (37 C) and thermophilic (55 C) temperatures. The hydrogen production yields with activated sludge at 37 C and 55 C were 0.56 and 1.32 mol H{sub 2}/mol glucose consumed, respectively. While with anaerobically digested sludge hydrogen yield was 2.18 mol H{sub 2}/mol glucose consumed at 37 C and 1.25 mol H{sub 2}/mol glucose consumed at 55 C. The results of repeated batch experiments for 615 h resulted in average yields of 1.21 {+-} 0.62 and 1.40 {+-} 0.16 mol H{sub 2}/mol glucose consumed for activated sludge and anaerobic sludge, respectively. The hydrogen production with activated sludge was not stable during the repeated batches and the fluctuation in hydrogen production was attributed to formation of lactic acid as the predominant metabolite in some batches. The presence of lactic acid bacteria in microflora was confirmed by PCR-DGGE. (author)

  5. Systematic Discrimination of Advanced Hydrogen Production Technologies

    Energy Technology Data Exchange (ETDEWEB)

    Charles V. Park; Michael W. Patterson

    2010-07-01

    The U.S. Department of Energy, in concert with industry, is developing a high-temperature gas-cooled reactor at the Idaho National Laboratory (INL) to demonstrate high temperature heat applications to produce hydrogen and electricity or to support other industrial applications. A key part of this program is the production of hydrogen from water that would significantly reduce carbon emissions compared to current production using natural gas. In 2009 the INL led the methodical evaluation of promising advanced hydrogen production technologies in order to focus future resources on the most viable processes. This paper describes how the evaluation process was systematically planned and executed. As a result, High-Temperature Steam Electrolysis was selected as the most viable near-term technology to deploy as a part of the Next Generation Nuclear Plant Project.

  6. 负载NiO-Fe2O3的凹凸棒石对生物油模型物催化重整制氢性能的影响%Hydrogen production via catalytic steam reforming of bio-oil model compounds over NiO-Fe2 O3-loaded palygouskite

    Institute of Scientific and Technical Information of China (English)

    王一双; 陈明强; 刘少敏; 杨忠连; 沈朝萍; 刘珂

    2015-01-01

    A series of NiO-Fe2 O3 catalysts loaded on palygouskite were prepared by co-precipitation method and used in the catalytic steam reforming to produce hydrogen in a self-made three-stage fixed bed reactor. The loading of NiO-Fe2 O3 , reaction temperature and ratio of steam to carbon ( S/C) on hydrogen production were investigated, with a water-soluble mixture of acetic acid, ethanol and phenol as the bio-oil model compounds. The results indicated that under the optimum conditions, viz. , 650 ° C, an S/C ratio of 8 ~10 and 50%NiO-50%Fe2 O3/PG as the catalyst, the relative content of H2 reaches 66. 15% in the gaseous product.%利用共沉淀法,制备一系列在凹凸棒土上负载不同含量的NiO-Fe2O3 催化剂. 以乙酸、乙醇和苯酚的水溶性溶液为生物油模型物,在自制的三段式固定床反应器中,考察了NiO-Fe2 O3 的负载量、反应温度、水碳比( S/C)对生物油模型物重整制氢的影响. 结果表明,所获得的氢气产率最高的工艺条件为,在650℃条件下,以水碳比8~10的生物油模型为实验原料,使用自制的50%NiO-50%Fe2 O3/PG型催化剂,可使气体产物中H2 的相对含量达到最大66. 15%.

  7. Determination of iron and aluminum based on the catalytic effect on the reaction of xylene cyanol FF with hydrogen peroxide and potassium periodate

    OpenAIRE

    Cai, Longfei; Xu, Chunxiu

    2011-01-01

    A simple, sensitive and selective method for the simultaneous determination of trace iron and aluminum by catalytic spectrophotometry is presented. This method is based on the catalytic effects of iron and aluminum on the reaction of xylene cyanol FF with hydrogen peroxide and potassium periodate. Both iron and aluminum did not show catalytic effects on the oxidation reaction of xylene cyanol FF in the presence of either hydrogen peroxide or potassium periodate. However, significant catalytic...

  8. Excellent catalytic effects of highly crumpled graphene nanosheets on hydrogenation/dehydrogenation of magnesium hydride

    Science.gov (United States)

    Liu, Guang; Wang, Yijing; Xu, Changchang; Qiu, Fangyuan; An, Cuihua; Li, Li; Jiao, Lifang; Yuan, Huatang

    2013-01-01

    Highly crumpled graphene nanosheets (GNS) with a BET surface area as high as 1159 m2 g-1 was fabricated by a thermal exfoliation method. A systematic investigation was performed on the hydrogen sorption properties of MgH2-5 wt% GNS nanocomposites acquired by ball-milling. It was found that the as-synthesized GNS exhibited a superior catalytic effect on hydrogenation/dehydrogenation of MgH2. Differential Scanning Calorimetry (DSC) and isothermal hydrogenation/dehydrogenation measurements indicated that both hydrogen sorption capacity and dehydrogenation/hydrogenation kinetics of the composites improved with increasing milling time. The composites MgH2-GNS milled for 20 h can absorb 6.6 wt% H2 within 1 min at 300 °C and 6.3 wt% within 40 min at 200 °C, even at 150 °C, it can also absorb 6.0 wt% H2 within 180 min. It was also demonstrated that MgH2-GNS-20 h could release 6.1 wt% H2 at 300 °C within 40 min. In addition, microstructure measurements based on XRD, SEM, TEM as well as Raman spectra revealed that the grain size of thus-prepared MgH2-GNS nanocomposites decreased with increasing milling time, moreover, the graphene layers were broken into smaller graphene nanosheets in a disordered and irregular manner during milling. It was confirmed that these smaller graphene nanosheets on the composite surface, providing more edge sites and hydrogen diffusion channels, prevented the nanograins from sintering and agglomerating, thus, leading to promotion of the hydrogenation/dehydrogenation kinetics of MgH2.Highly crumpled graphene nanosheets (GNS) with a BET surface area as high as 1159 m2 g-1 was fabricated by a thermal exfoliation method. A systematic investigation was performed on the hydrogen sorption properties of MgH2-5 wt% GNS nanocomposites acquired by ball-milling. It was found that the as-synthesized GNS exhibited a superior catalytic effect on hydrogenation/dehydrogenation of MgH2. Differential Scanning Calorimetry (DSC) and isothermal hydrogenation

  9. A Highly Efficient Heterogenized Iridium Complex for the Catalytic Hydrogenation of Carbon Dioxide to Formate.

    Science.gov (United States)

    Park, Kwangho; Gunasekar, Gunniya Hariyanandam; Prakash, Natarajan; Jung, Kwang-Deog; Yoon, Sungho

    2015-10-26

    A heterogenized catalyst on a highly porous covalent triazine framework was synthesized and characterized to have a coordination environment similar to that of its homogeneous counterpart. The catalyst efficiently converted CO2 into formate through hydrogenation with a turnover number of 5000 after 2 h and an initial turnover frequency of up to 5300 h(-1) ; both of these values are the highest reported to date for a heterogeneous catalyst, which makes it attractive toward industrial application. Furthermore, the synthesized catalyst was found to be stable in air and was recycled by simple filtration without significant loss of catalytic activity.

  10. An investigation of turbulent catalytically stabilized channel flow combustion of lean hydrogen - air mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Mantzaras, I.; Benz, P.; Schaeren, R.; Bombach, R. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    The catalytically stabilised thermal combustion (CST) of lean hydrogen-air mixtures was investigated numerically in a turbulent channel flow configuration using a two-dimensional elliptic model with detailed heterogeneous and homogeneous chemical reactions. Comparison between turbulent and laminar cases having the same incoming mean properties shows that turbulence inhibits homogeneous ignition due to increased heat transport away from the near-wall layer. The peak root-mean-square temperature and species fluctuations are always located outside the extent of the homogeneous reaction zone indicating that thermochemical fluctuations have no significant influence on gaseous combustion. (author) 4 figs., 6 refs.

  11. Review of Catalytic Hydrogen Generation in the Defense Waste Processing Facility (DWPF) Chemical Processing Cell

    Energy Technology Data Exchange (ETDEWEB)

    Koopman, D. C.

    2004-12-31

    This report was prepared to fulfill the Phase I deliverable for HLW/DWPF/TTR-98-0018, Rev. 2, ''Hydrogen Generation in the DWPF Chemical Processing Cell'', 6/4/2001. The primary objective for the preliminary phase of the hydrogen generation study was to complete a review of past data on hydrogen generation and to prepare a summary of the findings. The understanding was that the focus should be on catalytic hydrogen generation, not on hydrogen generation by radiolysis. The secondary objective was to develop scope for follow-up experimental and analytical work. The majority of this report provides a summary of past hydrogen generation work with radioactive and simulated Savannah River Site (SRS) waste sludges. The report also includes some work done with Hanford waste sludges and simulants. The review extends to idealized systems containing no sludge, such as solutions of sodium formate and formic acid doped with a noble metal catalyst. This includes general information from the literature, as well as the focused study done by the University of Georgia for the SRS. The various studies had a number of points of universal agreement. For example, noble metals, such as Pd, Rh, and Ru, catalyze hydrogen generation from formic acid and formate ions, and more acid leads to more hydrogen generation. There were also some points of disagreement between different sources on a few topics such as the impact of mercury on the noble metal catalysts and the identity of the most active catalyst species. Finally, there were some issues of potential interest to SRS that apparently have not been systematically studied, e.g. the role of nitrite ion in catalyst activation and reactivity. The review includes studies covering the period from about 1924-2002, or from before the discovery of hydrogen generation during simulant sludge processing in 1988 through the Shielded Cells qualification testing for Sludge Batch 2. The review of prior studies is followed by a

  12. Hydrogen production by aqueous phase reforming of light oxygenated hydrocarbons

    Science.gov (United States)

    Shabaker, John William

    Aqueous phase reforming (APR) of renewable oxygenated hydrocarbons (e.g., methanol, ethylene glycol, glycerol, sorbitol, glucose) is a promising new technology for the catalytic production of high-purity hydrogen for fuel cells and chemical processing. Supported Pt catalysts are effective catalysts for stable and rapid H2 production at temperatures near 500 K (H 2 turnover frequencies near 10 min-1). Inexpensive Raney Ni-based catalysts have been developed using a combination of fundamental and high-throughput studies that have similar catalytic properties as Pt-based materials. Promotion of Raney Ni with Sn by controlled surface reaction of organometallic tin compounds is necessary to control formation of thermodynamically-favorable alkane byproducts. Detailed characterization by Mossbauer spectroscopy, electron microscopy, adsorption studies, and x-ray photoelectron spectroscopy (XPS/ESCA) has shown that NiSn alloys are formed during heat treatment, and may be responsible for enhanced stability and selectivity for hydrogen production. Detailed kinetic studies led to the development of a kinetic mechanism for the APR reaction on Pt and NiSn catalysts, in which the oxygenate decomposes through C--H and O--H cleavage, followed by C--C cleavage and water gas shift of the CO intermediate. The rate limiting step on Pt surfaces is the initial dehydrogenation, while C--C cleavage appears rate limiting over NiSn catalysts. Tin promotion of Raney Ni catalysts suppresses C--O bond scission reactions that lead to alkane formation without inhibiting fast C--C and C--H cleavage steps that are necessary for high rates of reforming. A window of operating temperature, pressure, and reactor residence time has been identified for use of the inexpensive NiSn catalysts as a Pt substitute. Concentrated feed stocks and aggressive pretreatments have been found to counteract catalyst deactivation by sintering in the hydrothermal APR environment and allow stable, long-term production of H

  13. Dynamic\tmodelling of catalytic three-phase reactors for hydrogenation and oxidation processes

    Directory of Open Access Journals (Sweden)

    Salmi T.

    2000-01-01

    Full Text Available The dynamic modelling principles for typical catalytic three-phase reactors, batch autoclaves and fixed (trickle beds were described. The models consist of balance equations for the catalyst particles as well as for the bulk phases of gas and liquid. Rate equations, transport models and mass balances were coupled to generalized heterogeneous models which were solved with respect to time and space with algorithms suitable for stiff differential equations. The aspects of numerical solution strategies were discussed and the procedure was illustrated with three case studies: hydrogenation of aromatics, hydrogenation of aldehydes and oxidation of ferrosulphate. The case studies revealed the importance of mass transfer resistance inside the catalyst pallets as well as the dynamics of the different phases being present in the reactor. Reliable three-phase reactor simulation and scale-up should be based on dynamic heterogeneous models.

  14. Production of pure hydrogen by ethanol dehydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Santacesaria, E.; Carotenuto, G.; Tesser, R.; Di Serio, M. [Naples ' ' Federico II' ' Univ. (Italy). Dept. of Chemistry

    2010-12-30

    Hydrogen production from bio-ethanol is one of the most promising renewable processes to generate electricity using fuel cells. In this work, we have studied the production of pure hydrogen as by product of ethanol dehydrogenation reaction. This reaction is promoted by copper based catalysts and according to the catalyst used and the operative conditions gives place to acetaldehyde or ethyl acetate as main products. We studied in particular the performance of a commercial copper/copper chromite catalyst, supported on alumina and containing barium chromate as promoter that has given the best results. By operating at low pressure and temperature with short residence times, acetaldehyde is more selectively produced, while, by increasing the pressure (10-30 bars), the temperature (200-260 C) and the residence time (about 100 (grams hour/mol) of ethanol contact time) the selectivity is shifted to the production of ethyl acetate. However, in both cases pure hydrogen is obtained, as by product, that can easily be separated. Hydrogen obtained in this way is exempt of CO and can be directly fed to fuel cells without any inconvenience. In this work, runs performed in different operative conditions have been reported with the scope to individuate the best conditions. A carrier of H{sub 2} 6% in N{sub 2} has been used. The studied catalyst has also shown a good thermal stability with respect to sintering phenomena, that generally occurs during the dehydrogenation on other copper catalysts. Hydrogen productivities of 8-39 mol{sub H2} (gcat){sup -1}(h){sup -1} have been obtained for the explored temperature range 200-260 C. At last, the most accredited reaction mechanism is reported and discussed on the basis of the obtained results. (orig.)

  15. Hydrogen production by alkaline water electrolysis

    Directory of Open Access Journals (Sweden)

    Diogo M. F. Santos

    2013-01-01

    Full Text Available Water electrolysis is one of the simplest methods used for hydrogen production. It has the advantage of being able to produce hydrogen using only renewable energy. To expand the use of water electrolysis, it is mandatory to reduce energy consumption, cost, and maintenance of current electrolyzers, and, on the other hand, to increase their efficiency, durability, and safety. In this study, modern technologies for hydrogen production by water electrolysis have been investigated. In this article, the electrochemical fundamentals of alkaline water electrolysis are explained and the main process constraints (e.g., electrical, reaction, and transport are analyzed. The historical background of water electrolysis is described, different technologies are compared, and main research needs for the development of water electrolysis technologies are discussed.

  16. Hydrogen production by fermentative consortia

    Energy Technology Data Exchange (ETDEWEB)

    Valdez-Vazquez, Idania [Centro de Investigacion Cientifica y de Educacion Superior de Ensenada (CICESE), Department of Marine Biotechnology, Ensenada, B.C. Mexico (Mexico); Poggi-Varaldo, Hector M. [CINVESTAV-IPN, Department of Biotechnology and Bioengineering, PO Box 14-740, Mexico D.F. 07000 (Mexico)

    2009-06-15

    In this work, H{sub 2} production by anaerobic mixed cultures was reviewed. First, the different anaerobic microbial communities that have a direct relation with the generation or consumption of H{sub 2} are discussed. Then, the different methods used to inhibit the H{sub 2}-consuming bacteria are analyzed (mainly in the methanogenesis phase) such as biokinetic control (low pH and short hydraulic retention time), heat-shock treatment and chemical inhibitors along with their advantages/disadvantages for their application on an industrial scale. After that, biochemical pathways of carbohydrate degradation to H{sub 2}, organic acids and solvents are showed. Fourth, structure, diversity and dynamics of H{sub 2}-producers communities are detailed. Later, the hydrogenase structure and activity is related with H{sub 2} production. Also, the causes for H{sub 2} production inhibition are analyzed along with strategies to avoid it. Finally, immobilized-cells systems are presented as a way to enhance H{sub 2} production. (author)

  17. Biomass-to-hydrogen via fast pyrolysis and catalytic steam reforming

    Energy Technology Data Exchange (ETDEWEB)

    Chornet, E.; Wang, D.; Czernik, S. [National Renewable Energy Lab., Golden, CO (United States)] [and others

    1996-10-01

    Pyrolysis of lignocellulosic biomass and reforming the pyroligneous oils is being studied as a strategy for producing hydrogen. Novel technologies for the rapid pyrolysis of biomass have been developed in the past decade. They provide compact and efficient systems to transform biomass into vapors that are condensed to oils, with yields as high as 75-80 wt.% of the anhydrous biomass. This {open_quotes}bio-oil{close_quotes} is a mixture of aldehydes, alcohols, acids, oligomers from the constitutive carbohydrates and lignin, and some water derived from the dehydration reactions. Hydrogen can be produced by reforming the bio-oil or its fractions with steam. A process of this nature has the potential to be cost competitive with conventional means of producing hydrogen. The reforming facility can be designed to handle alternate feedstocks, such as natural gas and naphtha, if necessary. Thermodynamic modeling of the major constituents of the bio-oil has shown that reforming is possible within a wide range of temperatures and steam-to-carbon ratios. Existing catalytic data on the reforming of oxygenates have been studied to guide catalyst selection. Tests performed on a microreactor interfaced with a molecular beam mass spectrometer showed that, by proper selection of the process variables: temperature, steam-to-carbon ratio, gas hourly space velocity, and contact time, almost total conversion of carbon in the feed to CO and CO{sub 2} could be obtained. These tests also provided possible reaction mechanisms where thermal cracking competes with catalytic processes. Bench-scale, fixed bed reactor tests demonstrated high hydrogen yields from model compounds and carbohydrate-derived pyrolysis oil fractions. Reforming bio-oil or its fractions required proper dispersion of the liquid to avoid vapor-phase carbonization of the feed in the inlet to the reactor. A special spraying nozzle injector was designed and successfully tested with an aqueous fraction of bio-oil.

  18. Effect of hydrogen combustion reaction on the dehydrogenation of ethane in a fixed-bed catalytic membrane reactor

    Institute of Scientific and Technical Information of China (English)

    Masoud Hasany; Mohammad Malakootikhah; Vahid Rahmanian; Soheila Yaghmaei

    2015-01-01

    A two-dimensional non-isothermal mathematical model has been developed for the ethane dehydrogenation reaction in a fixed-bed catalytic membrane reactor. Since ethane dehydrogenation is an equilibrium reaction, removal of produced hydrogen by the membrane shifts the thermodynamic equilibrium to ethylene production. For further displacement of the dehydrogenation reaction, oxidative dehydrogenation method has been used. Since ethane dehydrogenation is an endothermic reaction, the energy produced by the oxidative dehydrogena-tion method is consumed by the dehydrogenation reaction. The results show that the oxidative dehydrogenation method generated a substantial improvement in the reactor performance in terms of high conversions and significant energy saving. It was also established that the sweep gas velocity in the shell side of the reactor is one of the most important factors in the effectiveness of the reactor.

  19. Electricity-mediated biological hydrogen production

    NARCIS (Netherlands)

    Geelhoed, J.S.; Hamelers, H.V.M.; Stams, A.J.M.

    2010-01-01

    Anaerobic bacteria have the ability to produce electricity from the oxidation of organic substrates. They also may use electricity to support chemical reactions that are energetically unfavorable. In the fermentation of sugars, hydrogen can be formed as one of the main products. However, a yield of

  20. Reactors Save Energy, Costs for Hydrogen Production

    Science.gov (United States)

    2014-01-01

    While examining fuel-reforming technology for fuel cells onboard aircraft, Glenn Research Center partnered with Garrettsville, Ohio-based Catacel Corporation through the Glenn Alliance Technology Exchange program and a Space Act Agreement. Catacel developed a stackable structural reactor that is now employed for commercial hydrogen production and results in energy savings of about 20 percent.

  1. Photobiological hydrogen production employing Spirulina Maxima

    Energy Technology Data Exchange (ETDEWEB)

    Ugas, A.J.; Sebastian, P.J. [CIE-UNAM, Morelos (Mexico); Duhakt, R.V.; Valencia, R.T. [IBT-UNAM, Cuernavaca, Morelos (Mexico)

    2003-07-01

    Efforts are being made to develop materials and processes for the renewable production of hydrogen. This paper described the biological production of hydrogen using microorganisms via the photosynthetic route. Several experiments were conducted to produce hydrogen from the biomass of a strain of photosynthetic Spirulina maxim. Conductimetry was used to quantify the results, along with its introduction in a proton exchange membrane (PEM) fuel cell. The current generated was then measured. Spirulina maxim was cultivated under illumination by magnetic agitation air bubbling. The biomass was concentrated by filtration with micro-porous nylon cloth. The algal biomass was quantified by dry weight and by spectrophotometry. The biomass underwent an anaerobic process in darkness, under a nitrogen flow for 30 minutes. The photosynthesis reaction and the production of the enzyme hydrogenase were induced by leaving the culture in agitation and under illumination for 30 minutes to 2 hours. Tests were conducted with and without the addition of 2 grams of sodium ditionite before the photosynthesis process and with the same incident radiation in the bioreactor, which was coupled to a PEM fuel cell. The electric current generated was measured. The results indicate that after a certain stage of cellular growth, Spirulina maxim was capable of producing hydrogen photosynthetically after a process of anaerobic darkness. The biological production of hydrogen was quantifiable by conductimetry and coupling the bioreactor to a PEM fuel cell. The sodium ditionite proved to be a strong reducing agent that inhibits the oxygen production during the photosynthesis process and allows the activation of the enzyme hydrogenase. 4 refs., 2 tabs.

  2. Effects of acido-basic support properties on the catalytic hydrogenation of acetylene on gold nano-particles

    Science.gov (United States)

    Manda, Abdullah Ahmed

    Metallic gold nanoparticles supported on gamma-Al2O 3 and magnesia-alumina mixed oxide, with different magnesia content have been prepared by sol-gel method and characterized by different techniques (inductive coupled plasma-mass spectroscopy (ICP-MS), XRD, BET surface area analysis, transmission electron microscopy (TEM), CO2 and NH 3 temperature programmed desorption (TPD), H2 temperature programmed reduction (TPR) and FTIR of adsorbed CO2). Such systems were found to produce catalysts with controllable acidity, varying from catalyst possessing large density of acidic and low density of basic sites, others with acidic and basic sites of equal strength and density, and others with large basic and low acid sites densities, respectively. The catalytic assessment of the generated acidity was carried out using 2-propanol decomposition as a test reaction. The results obtained indicate that the presence of magnesia and reduced gold nanopartilces has imparted the catalysts, 1%Au/4%Mg-Al 2O3 and 1%Au/8%Mg-Al2O3, with significant base-catalytic properties. Acetylene hydrogenation and formation of coke deposits were investigated on a gold catalyst supported on gamma-Al2O3 and gold supported on alumina-magnisia mixed oxide with different gold content; 1%Au/gamma-Al 2O3, 1%Au/15%Mg-Al2O3, 2%Au/15%Mg-Al 2O3 and 4%Au/15%Mg-Al2O3. The effect of the H2/C2H2 ratio was studied over a range of values. The catalytic activity and selectivity towards ethylene and other products were investigated at different reaction temperatures. Acetylene hydrogenation was investigated in the presence and absence of ethylene in stream. It is investigated that the adsorption of the triple bond is preferred over the double bond and during selective catalytic (SCR) of C2H2 the two hydrocarbons do not compete for the same adsorption sites. The deactivation of catalysts was studied by temperature programmed oxidation (TPO). Higher content of coke over 1%Au/Al2O3 catalyst was investigated in contrast to

  3. Preparation and Catalytic Activity of a Novel Nanocrystalline ZrO2 @C Composite for Hydrogen Storage in NaAlH4.

    Science.gov (United States)

    Zhang, Xin; Wu, Ruyan; Wang, Zeyi; Gao, Mingxia; Pan, Hongge; Liu, Yongfeng

    2016-12-19

    Sodium alanate (NaAlH4 ) has attracted intense interest as a prototypical high-density hydrogen-storage material. However, poor reversibility and slow kinetics limit its practical applications. Herein, a nanocrystalline ZrO2 @C catalyst was synthesized by using Uio-66(Zr) as a precursor and furfuryl alcohol (FA) as a carbon source. The as-synthesized ZrO2 @C exhibits good catalytic activity for the dehydrogenation and hydrogenation of NaAlH4 . The NaAlH4 -7 wt % ZrO2 @C sample released hydrogen starting from 126 °C and reabsorbed it starting from 54 °C, and these temperatures are lower by 71 and 36 °C, respectively, relative to pristine NaAlH4 . At 160 °C, approximately 5.0 wt % of hydrogen was released from the NaAlH4 -7 wt % ZrO2 @C sample within 250 min, and the dehydrogenation product reabsorbed approximately 4.9 wt % within 35 min at 140 °C and 100 bar of hydrogen. The catalytic function of the Zr-based active species is believed to contribute to the significantly reduced operating temperatures and enhanced kinetics.

  4. On-line catalytic upgrading of biomass fast pyrolysis products

    Institute of Scientific and Technical Information of China (English)

    LU Qiang; ZHU XiFeng; LI WenZhi; ZHANG Ying; CHEN DengYu

    2009-01-01

    Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) was employed to achieve fast pyrolysis of biomass and on-line analysis of the pyrolysis vapors. Four biomass materials (poplar wood, fir wood, cotton straw and rice husk) were pyrolyzed to reveal the difference among their products. Moreover, catalytic cracking of the pyrolysis vapors from cotton straw was performed by using five catalysts, including two microporous zeolites (HZSM-5 and HY) and three mesoporous catalysts (ZrO2&TiO2, SBA-15 and AI/SBA-15). The results showed that the distribution of the pyrolytic products from the four materials differed a little from each other, while catalytic cracking could significantly alter the pyrolytic products. Those important primary pyrolytic products such as levoglucosen, hydroxyacetaldehyde and 1-hydroxy-2-propanone were decreased greatly after catalysis. The two microporous zeolites were ef-fective to generate high yields of hydrocarbons, while the three mesoporous materials favored the formation of furan, furfural and other furan compounds, as well as acetic acid.

  5. CATALYTIC INTERACTIONS OF RHODIUM, RUTHENIUM, AND MERCURY DURING SIMULATED DWPF CPC PROCESSING WITH HYDROGEN GENERATION

    Energy Technology Data Exchange (ETDEWEB)

    Koopman, D

    2008-10-09

    Simulations of the Defense Waste Processing Facility (DWPF) Chemical Processing Cell (CPC) vessels were performed as part of the ongoing investigation into catalytic hydrogen generation. Rhodium, ruthenium, and mercury have been identified as the principal elemental factors affecting the peak hydrogen generation rate in the DWPF Sludge Receipt and Adjustment Tank (SRAT) for a given acid addition. The primary goal of this study is to identify any significant interactions between the three factors. Noble metal concentrations were similar to recent sludge batches. Rh ranged from 0.0026-0.013% and Ru ranged from 0.010-0.050% in the dried sludge solids, while initial Hg ranged from 0.5-2.5 wt%. An experimental matrix was developed to ensure that the existence of statistically significant two-way interactions could be determined without confounding of the main effects with the two-way interaction effects. The nominal matrix design consisted of twelve SRAT cycles. Testing included: a three factor (Rh, Ru, and Hg) study at two levels per factor (eight runs), two duplicate midpoint runs, and two additional replicate runs to assess reproducibility away from the midpoint. Midpoint testing can identify potential quadratic effects from the three factors. A single sludge simulant was used for all tests. Acid addition was kept effectively constant except to compensate for variations in the starting mercury concentration. Six Slurry Mix Evaporator (SME) cycles were performed to supplement the SME hydrogen generation database. Some of the preliminary findings from this study include: (1) Rh was linked to the maximum SRAT hydrogen generation rate in the first two hours after acid addition in preliminary statistical modeling. (2) Ru was linked conclusively to the maximum SRAT hydrogen generation rate in the last four hours of reflux in preliminary statistical modeling. (3) Increasing the ratio of Hg/Rh shifted the noble metal controlling the maximum SRAT hydrogen generation rate from

  6. Hydrogen Peroxide as a Sustainable Energy Carrier: Electrocatalytic Production of Hydrogen Peroxide and the Fuel Cell

    Science.gov (United States)

    Fukuzumi, Shunichi; Yamada, Yusuke; Karlin, Kenneth D.

    2012-01-01

    This review describes homogeneous and heterogeneous catalytic reduction of dioxygen with metal complexes focusing on the catalytic two-electron reduction of dioxygen to produce hydrogen peroxide. Whether two-electron reduction of dioxygen to produce hydrogen peroxide or four-electron O2-reduction to produce water occurs depends on the types of metals and ligands that are utilized. Those factors controlling the two processes are discussed in terms of metal-oxygen intermediates involved in the catalysis. Metal complexes acting as catalysts for selective two-electron reduction of oxygen can be utilized as metal complex-modified electrodes in the electrocatalytic reduction to produce hydrogen peroxide. Hydrogen peroxide thus produced can be used as a fuel in a hydrogen peroxide fuel cell. A hydrogen peroxide fuel cell can be operated with a one-compartment structure without a membrane, which is certainly more promising for the development of low-cost fuel cells as compared with two compartment hydrogen fuel cells that require membranes. Hydrogen peroxide is regarded as an environmentally benign energy carrier because it can be produced by the electrocatalytic two-electron reduction of O2, which is abundant in air, using solar cells; the hydrogen peroxide thus produced could then be readily stored and then used as needed to generate electricity through the use of hydrogen peroxide fuel cells. PMID:23457415

  7. Hydrogen Peroxide as a Sustainable Energy Carrier: Electrocatalytic Production of Hydrogen Peroxide and the Fuel Cell.

    Science.gov (United States)

    Fukuzumi, Shunichi; Yamada, Yusuke; Karlin, Kenneth D

    2012-11-01

    This review describes homogeneous and heterogeneous catalytic reduction of dioxygen with metal complexes focusing on the catalytic two-electron reduction of dioxygen to produce hydrogen peroxide. Whether two-electron reduction of dioxygen to produce hydrogen peroxide or four-electron O2-reduction to produce water occurs depends on the types of metals and ligands that are utilized. Those factors controlling the two processes are discussed in terms of metal-oxygen intermediates involved in the catalysis. Metal complexes acting as catalysts for selective two-electron reduction of oxygen can be utilized as metal complex-modified electrodes in the electrocatalytic reduction to produce hydrogen peroxide. Hydrogen peroxide thus produced can be used as a fuel in a hydrogen peroxide fuel cell. A hydrogen peroxide fuel cell can be operated with a one-compartment structure without a membrane, which is certainly more promising for the development of low-cost fuel cells as compared with two compartment hydrogen fuel cells that require membranes. Hydrogen peroxide is regarded as an environmentally benign energy carrier because it can be produced by the electrocatalytic two-electron reduction of O2, which is abundant in air, using solar cells; the hydrogen peroxide thus produced could then be readily stored and then used as needed to generate electricity through the use of hydrogen peroxide fuel cells.

  8. Assessment of biological Hydrogen production processes: A review

    Science.gov (United States)

    Najafpour, G. D.; Shahavi, M. H.; Neshat, S. A.

    2016-06-01

    Energy crisis created a special attention on renewable energy sources. Among these sources; hydrogen through biological processes is well-known as the most suitable and renewable energy sources. In terms of process yield, hydrogen production from various sources was evaluated. A summary of microorganisms as potential hydrogen producers discussed along with advantages and disadvantages of several bioprocesses. The pathway of photo-synthetic and dark fermentative organisms was discussed. In fact, the active enzymes involved in performance of biological processes for hydrogen generation were identified and their special functionalities were discussed. The influential factors affecting on hydrogen production were known as enzymes assisting liberation specific enzymes such as nitrogenase, hydrogenase and uptake hydrogenase. These enzymes were quite effective in reduction of proton and form active molecular hydrogen. Several types of photosynthetic systems were evaluated with intension of maximum hydrogen productivities. In addition dark fermentative and light intensities on hydrogen productions were evaluated. The hydrogen productivities of efficient hydrogen producing strains were evaluated.

  9. Selective Production of Aromatic Aldehydes from Heavy Fraction of Bio-oil via Catalytic Oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yan; Chang, Jie; Ouyang, Yong; Zheng, Xianwei [South China Univ. of Technology, Guangzhou (China)

    2014-06-15

    High value-added aromatic aldehydes (e. g. vanillin and syringaldehyde) were produced from heavy fraction of bio-oil (HFBO) via catalytic oxidation. The concept is based on the use of metalloporphyin as catalyst and hydrogen peroxide (H{sub 2}O{sub 2}) as oxidant under alkaline condition. The biomimetic catalyst cobalt(II)-sulfonated tetraphenylporphyrin (Co(TPPS{sub 4})) was prepared and characterized. It exhibited relative high activity in the catalytic oxidation of HFBO. 4.57 wt % vanillin and 1.58 wt % syringaldehyde were obtained from catalytic oxidation of HFBO, compared to 2.6 wt % vanillin and 0.86 wt % syringaldehyde without Co(TPPS{sub 4}). Moreover, a possible mechanism of HFBO oxidation using Co(TPPS{sub 4})/H{sub 2}O{sub 2} was proposed by the research of model compounds. The results showed that this is a promising and environmentally friendly method for production of aromatic aldehydes from HFBO under Co(TPPS{sub 4})/H{sub 2}O{sub 2} system.

  10. Bio-ethanol steam reforming: Insights on the mechanism for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Benito, M.; Sanz, J.L.; Isabel, R.; Padilla, R.; Daza, L. [Instituto de Catalisis y Petroleoquimica (CSIC), Campus Cantoblanco, 28049 Madrid (Spain); Arjona, R. [Greencell (ABENGOA BIOENERGIA), Av. de la Buhaira 2, 41018 Sevilla (Spain)

    2005-10-10

    New catalysts for hydrogen production by steam reforming of bio-ethanol have been developed. Catalytic tests have been performed at laboratory scale, with the reaction conditions demanded in a real processor: i.e. ethanol and water feed, without a diluent gas. Catalyst ICP0503 has shown high activity and good resistance to carbon deposition. Reaction results show total conversion, high selectivity to hydrogen (70%), CO{sub 2}, CO and CH{sub 4} being the only by-products obtained. The reaction yields 4.25mol of hydrogen by mol of ethanol fed, close to the thermodynamic equilibrium prediction. The temperature influence on the catalytic activity for this catalyst has been studied. Conversion reaches 100% at temperature higher than 600{sup o}C. In the light of reaction results obtained, a reaction mechanism for ethanol steam reforming is proposed. Long-term reaction experiments have been performed in order to study the stability of the catalytic activity. The excellent stability of the catalyst ICP0503 indicates that the reformed stream could be fed directly to a high temperature fuel cell (MCFC, SOFC) without a further purification treatment. These facts suggest that ICP0503 is a good candidate to be implemented in a bio-ethanol processor for hydrogen production to feed a fuel cell. (author)

  11. Red mud as an efficient, stable, and costfree catalyst for COx-free hydrogen production from ammonia

    OpenAIRE

    Uzun, Alper; Kurtoğlu, Samira Fatma

    2016-01-01

    Red mud, one of the mostly produced industrial wastes, was converted into a catalyst with exceptionally high and stable performance for hydrogen production from ammonia. Results showed that iron species produced after reduction of the HCl digested red mud were converted into epsilon-Fe2N during the induction period of ammonia decomposition reaction at 700 degrees C. The catalytic performance measurements indicated that the modified red mud catalyst provides a record high hydrogen production r...

  12. Hydrogen production using Ag-Pd/TiO2 bimetallic catalysts: is there a combined effect of surface plasmon resonance with the Schottky mechanism on the photo-catalytic activity?(Conference Presentation)

    Science.gov (United States)

    Nadeem, Muhammad Amtiaz; Idriss, Hicham; Al-Oufi, Maher; Ahmed, Khaja Wahab; Anjum, Dalaver H.

    2016-10-01

    A series of Ag-Pd/TiO2 catalysts have been prepared, characterized and tested for H2 production activities from water in the presence of organic sacrificial agents. The synergistic effect of metallic properties (plasmonic and Schottky mechanisms) was investigated. XPS results indicated that silver is present in the form of its oxides (Ag2O and AgO) at 0.2-0.4 wt. % loading while palladium is present as PdO and Pd metal at similar loading. However, metallic character for silver particles increases while that of palladium metal particles decreases with increasing their % in the investigated range (0-1 wt. %). HRTEM results coupled with EDX analyses indicated the presence of two types of Ag containing particles (large ones with about 4-6 nm and smaller ones with ca. 1nm in size). Palladium was only found forming Ag-Pd alloy/composite with a wide size distribution range between 10-60 nm. Both particles are composed of silver and palladium, however. Optimal photocatalytic H2 production rates were obtained for catalysts with a palladium to silver ratios between 4 and 1.5 in the case of bimetallic catalysts. In addition, H2 production rates showed linear dependency on plasmonic response of Ag. The study demonstrates that increased H2 production rates can be achieved from an understanding of plasmonic and Schottky properties of metals loaded on top of the semiconductor.

  13. Economical hydrogen production by electrolysis using nano pulsed DC

    OpenAIRE

    Dharmaraj C.H, AdishKumar S.

    2012-01-01

    Hydrogen is an alternate renewable eco fuel. The environmental friendly hydrogen production method is electrolysis. The cost of electrical energy input is major role while fixing hydrogen cost in the conventional direct current Electrolysis. Using nano pulse DC input make the input power less and economical hydrogen production can be established. In this investigation, a lab scale electrolytic cell developed and 0.58 mL/sec hydrogen/oxygen output is obtained using conventional and nano pulsed...

  14. Photobiological hydrogen production and carbon dioxide sequestration

    Science.gov (United States)

    Berberoglu, Halil

    Photobiological hydrogen production is an alternative to thermochemical and electrolytic technologies with the advantage of carbon dioxide sequestration. However, it suffers from low solar to hydrogen energy conversion efficiency due to limited light transfer, mass transfer, and nutrient medium composition. The present study aims at addressing these limitations and can be divided in three parts: (1) experimental measurements of the radiation characteristics of hydrogen producing and carbon dioxide consuming microorganisms, (2) solar radiation transfer modeling and simulation in photobioreactors, and (3) parametric experiments of photobiological hydrogen production and carbon dioxide sequestration. First, solar radiation transfer in photobioreactors containing microorganisms and bubbles was modeled using the radiative transport equation (RTE) and solved using the modified method of characteristics. The study concluded that Beer-Lambert's law gives inaccurate results and anisotropic scattering must be accounted for to predict the local irradiance inside a photobioreactor. The need for accurate measurement of the complete set of radiation characteristics of microorganisms was established. Then, experimental setup and analysis methods for measuring the complete set of radiation characteristics of microorganisms have been developed and successfully validated experimentally. A database of the radiation characteristics of representative microorganisms have been created including the cyanobacteria Anabaena variabilis, the purple non-sulfur bacteria Rhodobacter sphaeroides and the green algae Chlamydomonas reinhardtii along with its three genetically engineered strains. This enabled, for the first time, quantitative assessment of the effect of genetic engineering on the radiation characteristics of microorganisms. In addition, a parametric experimental study has been performed to model the growth, CO2 consumption, and H 2 production of Anabaena variabilis as functions of

  15. Study on commercial HTGR hydrogen production system

    Energy Technology Data Exchange (ETDEWEB)

    Nishihara, Tetsuo [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment; Hada, Kazuhiko [Japan Atomic Energy Research Inst., Naka, Ibaraki (Japan). Naka Fusion Research Establishment; Nishimura, Kuniyuki [Mitsubishi Research Institute, Tokyo (Japan)

    2000-07-01

    The Japanese energy demand in 2030 will increase up to 117% in comparison with one in 2000. We have to avoid a large consumption of fossil fuel that induces a large CO{sub 2} emission from viewpoint of global warming. Furthermore new energy resources expected to resolve global warming have difficulty to be introduced more because of their low energy density. As a result, nuclear power still has a possibility of large introduction to meet the increasing energy demand. On the other hand, in Japan, 40% of fossil fuels in the primary energy are utilized for power generation, and the remaining are utilized as a heat source. New clean energy is required to reduce the consumption of fossil fuels and hydrogen is expected as a alternative energy resource. Prediction of potential hydrogen demand in Japan is carried out and it is clarified that the demand will potentially increase up to 4% of total primary energy in 2050. In present, steam reforming method is the most economical among hydrogen generation processes and the cost of hydrogen production is about 7 to 8 yen/m{sup 3} in Europe and the United States and about 13 yen/m{sup 3} in Japan. JAERI has proposed for using the HTGR whose maximum core outlet temperature is at 950degC as a heat source in the steam reforming to reduced the consumption of fossil fuels and resulting CO{sub 2} emission. Based on the survey of the production rate and the required thermal energy in conventional industry, it is clarified that a hydrogen production system by the steam reforming is the best process for the commercial HTGR nuclear heat utilization. The HTGR steam reforming system and other candidate nuclear heat utilization systems are considered from viewpoint of system layout and economy. From the results, the hydrogen production cost in the HTGR stream reforming system is expected to be about 13.5 yen/m{sup 3} if the cost of nuclear heat of the HTGR is the same as one of the LWR. (author)

  16. Catalytic production of aromatics and olefins from plant materials

    Energy Technology Data Exchange (ETDEWEB)

    Haag, W.O.; Rodewald, P.G.; Weisz, P.B.

    1980-08-01

    Hydrocarbons and hydrocarbon-like plant materials offer the possibility of relatively simple and energy-efficient processing to liquid fuels or petrochemicals. The use of such highly reduced photosynthesis products as potential fuels has been advocated by Calvin and coworkers, and Buchanan and coworkers have evaluated several hundred plant species for the presence of hydrocarbons. The yield of extracted oils may exceed 10 wt % of the plant dry weight. Some field growth studies of the most promising of these plants are underway, e.g., by Calvin in California, by Native Plants, Inc., and by the Diamond Shamrock Co., in conjunction with the University of Arizona, mostly with Euphorbia and related genera. Exploratory studies were performed to determine if direct catalytic upgrading of the hydrocarbon-like plant constituents could be carried out. A preliminary report has been published recently. A variety of plant materials were shown to be upgraded to liquid premium fuels by relatively simple catalytic processing over Mobil's shape selective zeolite, ZSM-5. The present paper contains additional information on the conversion of a variety of plant materials with special emphasis on the production of petrochemicals, and discusses key mechanistic aspects of the reactions. Feedstocks were chosen to represent different types of plant materials: corn oil, castor oil and jojoba seed oil; plant extracts from Euphorbia lathyrus and Grindelia squarrosa; and hydrocarbons obtained by tapping of trees such as copaiba oil and natural rubber latex.

  17. Catalytic phi meson production in heavy-ion collisions

    CERN Document Server

    Kolomeitsev, E E

    2009-01-01

    The phi meson production on hyperons, pi Y --> phi Y and anti-kaons bar-K N--> phi Y is argued to be a new efficient source of phi mesons in a nucleus-nucleus collision. These reactions are not suppressed according to Okubo-Zweig-Izuka rule in contrast to the processes with non-strange particles in the entrance channels, pi B and BB with B=N,Delta. A rough estimate of the cross sections within a simple hadronic model shows that the cross sections of pi Y-->phi Y and bar-K N-->phi Y reactions can exceed that of the pi N--> phi N reaction by factors 50 and 60, respectively. In the hadrochemical model for nucleus-nucleus collisions at SIS and lower AGS energies we calculate the evolution of strange particle populations and phi meson production rate due to the new processes. It is found that the catalytic reactions can be operative if the maximal temperature in nucleus-nucleus collisions is larger than 130 MeV and the collision time is larger than 10 fm. A possible influence of the catalytic reactions on the cent...

  18. Catalytic decomposition of methane to COx-free hydrogen and carbon nanotubes over Co–W/MgO catalysts

    Directory of Open Access Journals (Sweden)

    Ahmed E. Awadallah

    2015-09-01

    Full Text Available Bimetallic catalysts containing a series of Co/W at 40/10, 30/20, 20/30 and 10/40 wt% supported on MgO with a total metal content of 50 wt% were prepared and used for the catalytic decomposition of methane to COx-free hydrogen and multi-walled carbon nanotubes (MWCNTs. The solid fresh and exhausted catalysts were characterized structurally and chemically through XRD, TPR, BET, TGA, TEM and Raman spectroscopy. The 40%Co–10%W/MgO catalyst exhibited the highest activity for the production of both hydrogen and MWCNTs. The formation of a large amount of non-interacted Co3O4 species is considered as the main reason for the catalyst superiority in its activity. On the contrary, catalysts formulations of 20%Co–30%W and 10%Co–40%W demonstrated the formation of a large amount of hardly reducible CoWO4 and MgWO4 particles causing lower activity of these catalysts toward methane decomposition as evidenced through the XRD and TPR results.

  19. Wax: A benign hydrogen-storage material that rapidly releases H2-rich gases through microwave-assisted catalytic decomposition

    Science.gov (United States)

    Gonzalez-Cortes, S.; Slocombe, D. R.; Xiao, T.; Aldawsari, A.; Yao, B.; Kuznetsov, V. L.; Liberti, E.; Kirkland, A. I.; Alkinani, M. S.; Al-Megren, H. A.; Thomas, J. M.; Edwards, P. P.

    2016-01-01

    Hydrogen is often described as the fuel of the future, especially for application in hydrogen powered fuel-cell vehicles (HFCV’s). However, its widespread implementation in this role has been thwarted by the lack of a lightweight, safe, on-board hydrogen storage material. Here we show that benign, readily-available hydrocarbon wax is capable of rapidly releasing large amounts of hydrogen through microwave-assisted catalytic decomposition. This discovery offers a new material and system for safe and efficient hydrogen storage and could facilitate its application in a HFCV. Importantly, hydrogen storage materials made of wax can be manufactured through completely sustainable processes utilizing biomass or other renewable feedstocks. PMID:27759014

  20. Ab initio molecular dynamics simulations for the role of hydrogen in catalytic reactions of furfural on Pd(111)

    Science.gov (United States)

    Xue, Wenhua; Dang, Hongli; Liu, Yingdi; Jentoft, Friederike; Resasco, Daniel; Wang, Sanwu

    2014-03-01

    In the study of catalytic reactions of biomass, furfural conversion over metal catalysts with the presence of hydrogen has attracted wide attention. We report ab initio molecular dynamics simulations for furfural and hydrogen on the Pd(111) surface at finite temperatures. The simulations demonstrate that the presence of hydrogen is important in promoting furfural conversion. In particular, hydrogen molecules dissociate rapidly on the Pd(111) surface. As a result of such dissociation, atomic hydrogen participates in the reactions with furfural. The simulations also provide detailed information about the possible reactions of hydrogen with furfural. Supported by DOE (DE-SC0004600). This research used the supercomputer resources of the XSEDE, the NERSC Center, and the Tandy Supercomputing Center.

  1. Hydrogen production in single chamber microbial electrolysis cells with stainless steel fiber felt cathodes

    Science.gov (United States)

    Su, Min; Wei, Liling; Qiu, Zhaozheng; Wang, Gang; Shen, Jianquan

    2016-01-01

    Microbial electrolysis cell (MEC) is a promising technology for sustainable production of hydrogen from biodegradable carbon sources. Employing a low-cost and high efficient cathode to replace platinum catalyzed cathode (Pt/C) for hydrogen generation is a challenge for commercialization of MEC. Here we show that a 3D macroporous stainless steel fiber felt (SSFF) with high electrochemical active surface area has an excellent catalytic activity for hydrogen generation, which is comparable to Pt/C cathode and superior to stainless steel mesh (SSM) cathode in the single-chamber MEC. The SSFF cathode (mean filter rating 100 μm) produces hydrogen at a rate of 3.66 ± 0.43 m3 H2 m-3d-1 (current density of 17.29 ± 1.68 A m-2), with a hydrogen recovery of 76.37 ± 15.04% and overall energy efficiency of 79.61 ± 13.07% at an applied voltage of 0.9 V. The performance of SSFF cathode improves over time due to a decrease in overpotential which caused by corrosion. These results demonstrate that SSFF can be a promising alternative for Pt catalytic cathode in MEC for hydrogen production.

  2. Hydrogen Production from Methanol Using Corona Discharges

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Hydrogen production at room temperature from liquid methanol has been conductedusing corona discharge. The content of water in methanol solution has a significant effect on thisproduction. When water concentration increases from 1.0 % to 16.7 %, the methanol conversionrate changes from 0.196 to 0.284 mol/h. An important finding in this investigation is theformation of ethylene glycol as a major by-product. The yield of ethylene glycol is ranged from0.0045 to 0.0075 mol/h based on the water content.

  3. A Technical and Economic Review of Solar Hydrogen Production Technologies

    Science.gov (United States)

    Wilhelm, Erik; Fowler, Michael

    2006-01-01

    Hydrogen energy systems are being developed to replace fossil fuels-based systems for transportation and stationary application. One of the challenges facing the widespread adoption of hydrogen as an energy vector is the lack of an efficient, economical, and sustainable method of hydrogen production. In the short term, hydrogen produced from…

  4. High performing and stable supported nano-alloys for the catalytic hydrogenation of levulinic acid to gamma-valerolactone

    NARCIS (Netherlands)

    Luo, Wenhao; Meenakshisundaram, Sankar; Beale, Andrew M.; He, Qian; Kiely, Christopher J.; Bruijnincx, Pieter C. A.; Weckhuysen, Bert M.

    2015-01-01

    The catalytic hydrogenation of levulinic acid, a key platform molecule in many biorefinery schemes, into gamma-valerolactone is considered as one of the pivotal reactions to convert lignocellulose-based biomass into renewable fuels and chemicals. Here we report on the development of highly active, s

  5. Catalytic Hydrogenation ofα,β-Epoxyketones to β-Hydroxy-ketones with Two Sulfinyl Analogues of Coenzyme NADH Models

    Institute of Scientific and Technical Information of China (English)

    XIE,Kun; GUI,Yi; LIU,You-Cheng; FU,Yao

    2007-01-01

    An efficient method for the selective hydrogenation of a series of α,β-epoxyketones to β-hydroxyketones using catalytic amount of two sulfinyl analogues of NAD+ model compounds is reported. The lack of any diastereoselectivily for the formation of β-hydroxyketones with optically pure sulfinyl analogue of NAD+ model supports the radical mechanism proposed previously.

  6. β-Molybdenum nitride: synthesis mechanism and catalytic response in the gas phase hydrogenation of p-chloronitrobenzene

    NARCIS (Netherlands)

    Cárdenas-Lizana, F.; Gómez-Quero, S.; Perret, N.; Kiwi-Minsker, L.; Keane, M.A.

    2011-01-01

    A temperature programmed treatment of MoO3 in flowing N2 + H2 has been employed to prepare β-phase molybdenum nitride (β-Mo2N) which has been used to promote, for the first time, the catalytic hydrogenation of p-chloronitrobenzene. The reduction/nitridation synthesis steps have been monitored in sit

  7. The role of sulfur trapped in micropores in the catalytic partial oxidation of hydrogen sulfide with oxygen

    NARCIS (Netherlands)

    Steijns, M.; Mars, P.

    1974-01-01

    The catalytic oxidation of hydrogen sulfide into sulfur with molecular oxygen has been studied in the temperature range 130–200 °C. Active carbon, molecular sieve 13X and liquid sulfur were used as catalysts. Sulfur is adsorbed in the micropores (3 < r < 40 Å) of the catalysts. Experiments with a su

  8. Integrated Ceramic Membrane System for Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Schwartz, Joseph; Lim, Hankwon; Drnevich, Raymond

    2010-08-05

    Phase I was a technoeconomic feasibility study that defined the process scheme for the integrated ceramic membrane system for hydrogen production and determined the plan for Phase II. The hydrogen production system is comprised of an oxygen transport membrane (OTM) and a hydrogen transport membrane (HTM). Two process options were evaluated: 1) Integrated OTM-HTM reactor – in this configuration, the HTM was a ceramic proton conductor operating at temperatures up to 900°C, and 2) Sequential OTM and HTM reactors – in this configuration, the HTM was assumed to be a Pd alloy operating at less than 600°C. The analysis suggested that there are no technical issues related to either system that cannot be managed. The process with the sequential reactors was found to be more efficient, less expensive, and more likely to be commercialized in a shorter time than the single reactor. Therefore, Phase II focused on the sequential reactor system, specifically, the second stage, or the HTM portion. Work on the OTM portion was conducted in a separate program. Phase IIA began in February 2003. Candidate substrate materials and alloys were identified and porous ceramic tubes were produced and coated with Pd. Much effort was made to develop porous substrates with reasonable pore sizes suitable for Pd alloy coating. The second generation of tubes showed some improvement in pore size control, but this was not enough to get a viable membrane. Further improvements were made to the porous ceramic tube manufacturing process. When a support tube was successfully coated, the membrane was tested to determine the hydrogen flux. The results from all these tests were used to update the technoeconomic analysis from Phase I to confirm that the sequential membrane reactor system can potentially be a low-cost hydrogen supply option when using an existing membrane on a larger scale. Phase IIB began in October 2004 and focused on demonstrating an integrated HTM/water gas shift (WGS) reactor to

  9. SYNTHESIS OF POLYMER-STABILIZED PLATINUM/RUTHENIUM BIMETALLIC COLLOIDS AND THEIR CATALYTIC PROPERTIES FOR SELECTIVE HYDROGENATION OF CROTONALDEHYDE

    Institute of Scientific and Technical Information of China (English)

    Wei-xia Tu; Han-fan Liu

    2005-01-01

    Polymer-stabilized platinum/ruthenium bimetallic colloids (Pt/Ru) were synthesized by polyol reduction with microwave irradiation and characterized by TEM and XPS. The colloidal nanoparticles have small and narrow size distributions. Catalytic performance of the Pt/Ru colloidal catalysts was investigated on the selective hydrogenation of crontonaldehyde (CRAL). A suitable amount of the added metal ions and base can improve the selectivity of CRAL to crotylalcohol (CROL) remarkably. The catalytic activity and the selectivity are dependent on the compositions of bimetallic colloids. Thereinto, PVP-stabilized 9Pt/1Ru colloid with a molar ratio of metals Pt:Ru = 9:1 shows the highest catalytic selectivity 77.3% to CROL at 333 K under 4.0 MPa of hydrogen.

  10. Single-catalyst high-weight% hydrogen storage in an N-heterocycle synthesized from lignin hydrogenolysis products and ammonia

    Science.gov (United States)

    Forberg, Daniel; Schwob, Tobias; Zaheer, Muhammad; Friedrich, Martin; Miyajima, Nobuyoshi; Kempe, Rhett

    2016-10-01

    Large-scale energy storage and the utilization of biomass as a sustainable carbon source are global challenges of this century. The reversible storage of hydrogen covalently bound in chemical compounds is a particularly promising energy storage technology. For this, compounds that can be sustainably synthesized and that permit high-weight% hydrogen storage would be highly desirable. Herein, we report that catalytically modified lignin, an indigestible, abundantly available and hitherto barely used biomass, can be harnessed to reversibly store hydrogen. A novel reusable bimetallic catalyst has been developed, which is able to hydrogenate and dehydrogenate N-heterocycles most efficiently. Furthermore, a particular N-heterocycle has been identified that can be synthesized catalytically in one step from the main lignin hydrogenolysis product and ammonia, and in which the new bimetallic catalyst allows multiple cycles of high-weight% hydrogen storage.

  11. Single-catalyst high-weight% hydrogen storage in an N-heterocycle synthesized from lignin hydrogenolysis products and ammonia.

    Science.gov (United States)

    Forberg, Daniel; Schwob, Tobias; Zaheer, Muhammad; Friedrich, Martin; Miyajima, Nobuyoshi; Kempe, Rhett

    2016-10-20

    Large-scale energy storage and the utilization of biomass as a sustainable carbon source are global challenges of this century. The reversible storage of hydrogen covalently bound in chemical compounds is a particularly promising energy storage technology. For this, compounds that can be sustainably synthesized and that permit high-weight% hydrogen storage would be highly desirable. Herein, we report that catalytically modified lignin, an indigestible, abundantly available and hitherto barely used biomass, can be harnessed to reversibly store hydrogen. A novel reusable bimetallic catalyst has been developed, which is able to hydrogenate and dehydrogenate N-heterocycles most efficiently. Furthermore, a particular N-heterocycle has been identified that can be synthesized catalytically in one step from the main lignin hydrogenolysis product and ammonia, and in which the new bimetallic catalyst allows multiple cycles of high-weight% hydrogen storage.

  12. Novel Fast Pyrolysis/Catalytic Technology for the Production of Stable Upgraded Liquids

    Energy Technology Data Exchange (ETDEWEB)

    Oyama, Ted; Agblevor, Foster; Battaglia, Francine; Klein, Michael

    2013-01-18

    The objective of the proposed research is the demonstration and development of a novel biomass pyrolysis technology for the production of a stable bio-oil. The approach is to carry out catalytic hydrodeoxygenation (HDO) and upgrading together with pyrolysis in a single fluidized bed reactor with a unique two-level design that permits the physical separation of the two processes. The hydrogen required for the HDO will be generated in the catalytic section by the water-gas shift reaction employing recycled CO produced from the pyrolysis reaction itself. Thus, the use of a reactive recycle stream is another innovation in this technology. The catalysts will be designed in collaboration with BASF Catalysts LLC (formerly Engelhard Corporation), a leader in the manufacture of attrition-resistant cracking catalysts. The proposed work will include reactor modeling with state-of-the-art computational fluid dynamics in a supercomputer, and advanced kinetic analysis for optimization of bio-oil production. The stability of the bio-oil will be determined by viscosity, oxygen content, and acidity determinations in real and accelerated measurements. A multi-faceted team has been assembled to handle laboratory demonstration studies and computational analysis for optimization and scaleup.

  13. Kinetic models for fermentative hydrogen production: A review

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jianlong; Wan, Wei [Laboratory of Environmental Technology, INET, Tsinghua University, Beijing 100084 (China)

    2009-05-15

    The kinetic models were developed and applied for fermentative hydrogen production. They were used to describe the progress of a batch fermentative hydrogen production process, to investigate the effects of substrate concentration, inhibitor concentration, temperatures, pH, and dilution rates on the process of fermentative hydrogen production, and to establish the relationship among the substrate degradation rate, the hydrogen-producing bacteria growth rate and the product formation rate. This review showed that the modified Gompertz model was widely used to describe the progress of a batch fermentative hydrogen production process, while the Monod model was widely used to describe the effects of substrate concentration on the rates of substrate degradation, hydrogen-producing bacteria growth and hydrogen production. Arrhenius model was used a lot to describe the effects of temperature on fermentative hydrogen production, while modified Han-Levenspiel model was used to describe the effects of inhibitor concentration on fermentative hydrogen production. The Andrew model was used to describe the effects of H{sup +} concentration on the specific hydrogen production rate, while the Luedeking-Piret model and its modified form were widely used to describe the relationship between the hydrogen-producing bacteria growth rate and the product formation rate. Finally, some suggestions for future work with these kinetic models were proposed. (author)

  14. Resource Assessment for Hydrogen Production: Hydrogen Production Potential from Fossil and Renewable Energy Resources

    Energy Technology Data Exchange (ETDEWEB)

    Melaina, M. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Penev, M. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Heimiller, D. [National Renewable Energy Lab. (NREL), Golden, CO (United States)

    2013-09-01

    This study examines the energy resources required to produce 4-10 million metric tonnes of domestic, low-carbon hydrogen in order to fuel approximately 20-50 million fuel cell electric vehicles. These projected energy resource requirements are compared to current consumption levels, projected 2040 business as usual consumptions levels, and projected 2040 consumption levels within a carbonconstrained future for the following energy resources: coal (assuming carbon capture and storage), natural gas, nuclear (uranium), biomass, wind (on- and offshore), and solar (photovoltaics and concentrating solar power). The analysis framework builds upon previous analysis results estimating hydrogen production potentials and drawing comparisons with economy-wide resource production projections

  15. Production of hydrogen from municipal solid waste

    Energy Technology Data Exchange (ETDEWEB)

    Coleman, S.L.

    1995-11-01

    The Gasification of Municipal Solid Waste (MSW) includes gasification and the process for producing a gasificable slurry from raw MSW by using high pressures of steam. A potential energy source, MSW is a composite of organic materials such as: paper, wood, food waste, etc. There are different paper grades producing different results with low-quality paper forming better slurries than high-quality papers; making MSW a difficult feedstock for gasification. The objective of the bench-scale laboratory work has been to establish operating conditions for a hydrothermal pre-processing scheme for municipal solid waste (MSW) that produces a good slurry product that can be pumped and atomized to the gasifier for the production of hydrogen. Batch reactors are used to determine product yields as a function of hydrothermal treatment conditions. Various ratios of water-to-paper were used to find out solid product, gas product, and soluble product yields of MSW. Experimental conditions covered were temperature, time, and water to feed ratio. Temperature had the strongest effect on product yields.

  16. Production of hydrogen using an anaerobic biological process

    Energy Technology Data Exchange (ETDEWEB)

    Kramer, Robert; Pelter, Libbie S.; Patterson, John A.

    2016-11-29

    Various embodiments of the present invention pertain to methods for biological production of hydrogen. More specifically, embodiments of the present invention pertain to a modular energy system and related methods for producing hydrogen using organic waste as a feed stock.

  17. Hydrogen production by biological processes: a survey of literature

    Energy Technology Data Exchange (ETDEWEB)

    Das, Debabrata [Indian Inst. of Technology, Dept. of Biotechnology, Kharagpur (India); Miami Univ., Clean Energy Research Inst., Coral Gables, FL (United States); Veziroglu, T. Nejat [Miami Univ., Clean Energy Research Inst., Coral Gables, FL (United States)

    2001-07-01

    Hydrogen is the fuel of the future mainly due to its high conversion efficiency, recyclability and nonpolluting nature. Biological hydrogen production processes are found to be more environment friendly and less energy intensive as compared to thermochemical and electrochemical processes. They are mostly controlled by either photosynthetic or fermentative organisms. Till today, more emphasis has been given on the former processes. Nitrogenase and hydrogenase play very important roles. Genetic manipulation of cyanobacteria (hydrogenase negative gene) improves the hydrogen generation. The paper presents a survey of biological hydrogen production processes. The micro-organism and biochemical pathways involved in hydrogen generation processes are presented in some detail. Several developmental works are discussed. Immobilised system is found suitable for the continuous hydrogen production. About 28% of energy can be recovered in the form of hydrogen using sucrose as substrate. Fermentative hydrogen production processes have some edge over the other biological processes. (Author)

  18. Hydrogen Research for Spaceport and Space-Based Applications: Hydrogen Production, Storage, and Transport. Part 3

    Science.gov (United States)

    Anderson, Tim; Balaban, Canan

    2008-01-01

    The activities presented are a broad based approach to advancing key hydrogen related technologies in areas such as fuel cells, hydrogen production, and distributed sensors for hydrogen-leak detection, laser instrumentation for hydrogen-leak detection, and cryogenic transport and storage. Presented are the results from research projects, education and outreach activities, system and trade studies. The work will aid in advancing the state-of-the-art for several critical technologies related to the implementation of a hydrogen infrastructure. Activities conducted are relevant to a number of propulsion and power systems for terrestrial, aeronautics and aerospace applications. Hydrogen storage and in-space hydrogen transport research focused on developing and verifying design concepts for efficient, safe, lightweight liquid hydrogen cryogenic storage systems. Research into hydrogen production had a specific goal of further advancing proton conducting membrane technology in the laboratory at a larger scale. System and process trade studies evaluated the proton conducting membrane technology, specifically, scale-up issues.

  19. Plasma processing methods for hydrogen production

    Science.gov (United States)

    Mizeraczyk, Jerzy; Jasiński, Mariusz

    2016-08-01

    In the future a transfer from the fossil fuel-based economy to hydrogen-based economy is expected. Therefore the development of systems for efficient H2 production becomes important. The several conventional methods of mass-scale (or central) H2 production (methane, natural gas and higher hydrocarbons reforming, coal gasification reforming) are well developed and their costs of H2 production are acceptable. However, due to the H2 transport and storage problems the small-scale (distributed) technologies for H2 production are demanded. However, these new technologies have to meet the requirement of producing H2 at a production cost of (1-2)/kg(H2) (or 60 g(H2)/kWh) by 2020 (the U.S. Department of Energy's target). Recently several plasma methods have been proposed for the small-scale H2 production. The most promising plasmas for this purpose seems to be those generated by gliding, plasmatron and nozzle arcs, and microwave discharges. In this paper plasma methods proposed for H2 production are briefly described and critically evaluated from the view point of H2 production efficiency. The paper is aiming at answering a question if any plasma method for the small-scale H2 production approaches such challenges as the production energy yield of 60 g(H2)/kWh, high production rate, high reliability and low investment cost. Contribution to the topical issue "6th Central European Symposium on Plasma Chemistry (CESPC-6)", edited by Nicolas Gherardi, Ester Marotta and Cristina Paradisi

  20. Biological hydrogen production using a membrane bioreactor.

    Science.gov (United States)

    Oh, Sang-Eun; Iyer, Prabha; Bruns, Mary Ann; Logan, Bruce E

    2004-07-01

    A cross-flow membrane was coupled to a chemostat to create an anaerobic membrane bioreactor (MBR) for biological hydrogen production. The reactor was fed glucose (10,000 mg/L) and inoculated with a soil inoculum heat-treated to kill non-spore-forming methanogens. Hydrogen gas was consistently produced at a concentration of 57-60% in the headspace under all conditions. When operated in chemostat mode (no flow through the membrane) at a hydraulic retention time (HRT) of 3.3 h, 90% of the glucose was removed, producing 2200 mg/L of cells and 500 mL/h of biogas. When operated in MBR mode, the solids retention time (SRT) was increased to SRT = 12 h producing a solids concentration in the reactor of 5800 mg/L. This SRT increased the overall glucose utilization (98%), the biogas production rate (640 mL/h), and the conversion efficiency of glucose-to-hydrogen from 22% (no MBR) to 25% (based on a maximum of 4 mol-H(2)/mol-glucose). When the SRT was increased from 5 h to 48 h, glucose utilization (99%) and biomass concentrations (8,800 +/- 600 mg/L) both increased. However, the biogas production decreased (310 +/- 40 mL/h) and the glucose-to-hydrogen conversion efficiency decreased from 37 +/- 4% to 18 +/- 3%. Sustained permeate flows through the membrane were in the range of 57 to 60 L/m(2) h for three different membrane pore sizes (0.3, 0.5, and 0.8 microm). Most (93.7% to 99.3%) of the membrane resistance was due to internal fouling and the reversible cake resistance, and not the membrane itself. Regular backpulsing was essential for maintaining permeate flux through the membrane. Analysis of DNA sequences using ribosomal intergenic spacer analysis indicated bacteria were most closely related to members of Clostridiaceae and Flexibacteraceae, including Clostridium acidisoli CAC237756 (97%), Linmingia china AF481148 (97%), and Cytophaga sp. MDA2507 AF238333 (99%). No PCR amplification of 16s rRNA genes was obtained when archaea-specific primers were used.

  1. Hydrogenation-controlled phase transition on two-dimensional transition metal dichalcogenides and their unique physical and catalytic properties

    Science.gov (United States)

    Qu, Yuanju; Pan, Hui; Kwok, Chi Tat

    2016-09-01

    Two-dimensional (2D) transition metal dichalcogenides (TMDs) have been widely used from nanodevices to energy harvesting/storage because of their tunable physical and chemical properties. In this work, we systematically investigate the effects of hydrogenation on the structural, electronic, magnetic, and catalytic properties of 33 TMDs based on first-principles calculations. We find that the stable phases of TMD monolayers can transit from 1T to 2H phase or vice versa upon the hydrogenation. We show that the hydrogenation can switch their magnetic and electronic states accompanying with the phase transition. The hydrogenation can tune the magnetic states of TMDs among non-, ferro, para-, and antiferro-magnetism and their electronic states among semiconductor, metal, and half-metal. We further show that, out of 33 TMD monolayers, 2H-TiS2 has impressive catalytic ability comparable to Pt in hydrogen evolution reaction in a wide range of hydrogen coverages. Our findings would shed the light on the multi-functional applications of TMDs.

  2. Alkane production from biomass: chemo-, bio- and integrated catalytic approaches.

    Science.gov (United States)

    Deneyer, Aron; Renders, Tom; Van Aelst, Joost; Van den Bosch, Sander; Gabriëls, Dries; Sels, Bert F

    2015-12-01

    Linear, branched and cyclic alkanes are important intermediates and end products of the chemical industry and are nowadays mainly obtained from fossil resources. In search for alternatives, biomass feedstocks are often presented as a renewable carbon source for the production of fuels, chemicals and materials. However, providing a complete market for all these applications seems unrealistic due to both financial and logistic issues. Despite the very large scale of current alkane-based fuel applications, biomass definitely has the potential to offer a partial solution to the fuel business. For the smaller market of chemicals and materials, a transition to biomass as main carbon source is more realistic and even probably unavoidable in the long term. The appropriate use and further development of integrated chemo- and biotechnological (catalytic) process strategies will be crucial to successfully accomplish this petro-to-bio feedstock transition. Furthermore, a selection of the most promising technologies from the available chemo- and biocatalytic tool box is presented. New opportunities will certainly arise when multidisciplinary approaches are further explored in the future. In an attempt to select the most appropriate biomass sources for each specific alkane-based application, a diagram inspired by van Krevelen is applied, taking into account both the C-number and the relative functionality of the product molecules.

  3. Field-controlled electron transfer and reaction kinetics of the biological catalytic system of microperoxidase-11 and hydrogen peroxide

    Directory of Open Access Journals (Sweden)

    Yongki Choi

    2011-12-01

    Full Text Available Controlled reaction kinetics of the bio-catalytic system of microperoxidase-11 and hydrogen peroxide has been achieved using an electrostatic technique. The technique allowed independent control of 1 the thermodynamics of the system using electrochemical setup and 2 the quantum mechanical tunneling at the interface between microperoxidase-11 and the working electrode by applying a gating voltage to the electrode. The cathodic currents of electrodes immobilized with microperoxidase-11 showed a dependence on the gating voltage in the presence of hydrogen peroxide, indicating a controllable reduction reaction. The measured kinetic parameters of the bio-catalytic reduction showed nonlinear dependences on the gating voltage as the result of modified interfacial electron tunnel due to the field induced at the microperoxidase-11-electrode interface. Our results indicate that the kinetics of the reduction of hydrogen peroxide can be controlled by a gating voltage and illustrate the operation of a field-effect bio-catalytic transistor, whose current-generating mechanism is the conversion of hydrogen peroxide to water with the current being controlled by the gating voltage.

  4. Hydrogen in the Methanol Production Process

    Science.gov (United States)

    Kralj, Anita Kovac; Glavic, Peter

    2006-01-01

    Hydrogen is a very important industrial gas in chemical processes. It is very volatile; therefore, it can escape from the process units and its mass balance is not always correct. In many industrial processes where hydrogen is reacted, kinetics are often related to hydrogen pressure. The right thermodynamic properties of hydrogen can be found for…

  5. Bio-Inspired Molecular Catalysts for Hydrogen Oxidation and Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Ho, Ming-Hsun; Chen, Shentan; Rousseau, Roger J.; Dupuis, Michel; Bullock, R. Morris; Raugei, Simone

    2013-06-03

    Recent advances in Ni-based bio-inspired catalysts obtained in the Center for Molecular Electrocatalysis, an Energy Frontier Research Center (EFRC) at the Pacific Northwest National Laboratory, demonstrated the possibility of cleaving H2 or generating H2 heterolytically with turnover frequencies comparable or superior to those of hydrogenase enzymes. In these catalysts the transformation between H2 and protons proceeds via an interplay between proton, hydride and electron transfer steps and involves the interaction of a dihydrogen molecule with both a Ni(II) center and with pendant amine bases incorporated in a six-membered ring, which act as proton relays. These catalytic platforms are well designed in that when protons are correctly positioned (endo) toward the Raugei-ACS-Books.docxPrinted 12/18/12 2 metal center, catalysis proceeds at very high rates. We will show that the proton removal (for H2 oxidation) and proton delivery (for H2 production) are often the rate determining steps. Furthermore, the presence of multiple protonation sites gives rise to reaction intermediates with protons not correctly positioned (exo relative to the metal center). These isomers are easily accessible kinetically and are detrimental to catalysis because of the slow isomerization processes necessary to convert them to the catalytically competent endo isomers. In this chapter we will review the major findings of our computational investigation on the role of proton relays for H2 chemistry and provide guidelines for the design of new catalysts. This research was carried out in the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science. Pacific Northwest National Laboratory is operated for the U.S. Department of Energy by Battelle. Computational resources were provided at W. R. Wiley Environmental Molecular Science Laboratory (EMSL), a Raugei-Bio-Inspired Molecular-Catalysts-for-Hydrogen- Oxidation-and-Hydrogen-Production

  6. Production of Low-carbon Light Olefins from Catalytic Cracking of Crude Bio-oil

    Institute of Scientific and Technical Information of China (English)

    Yan-ni Yuan; Tie-jun Wang; Quan-xin Li

    2013-01-01

    Low-carbon light olefins are the basic feedstocks for the petrochemical industry.Catalytic cracking of crude bio-oil and its model compounds (including methanol,ethanol,acetic acid,acetone,and phenol) to light olefins were performed by using the La/HZSM-5 catalyst.The highest olefins yield from crude bio-oil reached 0.19 kg/(kg crude bio-oil).The reaction conditions including temperature,weight hourly space velocity,and addition of La into the HZSM-5 zeolite can be used to control both olefins yield and selectivity.Moderate adjusting the acidity with a suitable ratio between the strong acid and weak acid sites through adding La to the zeolite effectively enhanced the olefins selectivity and improved the catalyst stability.The production of light olefins from crude bio-oil is closely associated with the chemical composition and hydrogen to carbon effective ratios of feedstock.The comparison between the catalytic cracking and pyrolysis of bio-oil was studied.The mechanism of the bio-oil conversion to light olefins was also discussed.

  7. Hydrogen Gas Production from Nuclear Power Plant in Relation to Hydrogen Fuel Cell Technologies Nowadays

    Science.gov (United States)

    Yusibani, Elin; Kamil, Insan; Suud, Zaki

    2010-06-01

    Recently, world has been confused by issues of energy resourcing, including fossil fuel use, global warming, and sustainable energy generation. Hydrogen may become the choice for future fuel of combustion engine. Hydrogen is an environmentally clean source of energy to end-users, particularly in transportation applications because without release of pollutants at the point of end use. Hydrogen may be produced from water using the process of electrolysis. One of the GEN-IV reactors nuclear projects (HTGRs, HTR, VHTR) is also can produce hydrogen from the process. In the present study, hydrogen gas production from nuclear power plant is reviewed in relation to commercialization of hydrogen fuel cell technologies nowadays.

  8. Catalytic effect of nanoparticle 3d-transition metals on hydrogen storage properties in magnesium hydride MgH2 prepared by mechanical milling.

    Science.gov (United States)

    Hanada, Nobuko; Ichikawa, Takayuki; Fujii, Hironobu

    2005-04-21

    We examined the catalytic effect of nanoparticle 3d-transition metals on hydrogen desorption (HD) properties of MgH(2) prepared by mechanical ball milling method. All the MgH(2) composites prepared by adding a small amount of nanoparticle Fe(nano), Co(nano), Ni(nano), and Cu(nano) metals and by ball milling for 2 h showed much better HD properties than the pure ball-milled MgH(2) itself. In particular, the 2 mol % Ni(nano)-doped MgH(2) composite prepared by soft milling for a short milling time of 15 min under a slow milling revolution speed of 200 rpm shows the most superior hydrogen storage properties: A large amount of hydrogen ( approximately 6.5 wt %) is desorbed in the temperature range from 150 to 250 degrees C at a heating rate of 5 degrees C/min under He gas flow with no partial pressure of hydrogen. The EDX micrographs corresponding to Mg and Ni elemental profiles indicated that nanoparticle Ni metals as catalyst homogeneously dispersed on the surface of MgH(2). In addition, it was confirmed that the product revealed good reversible hydriding/dehydriding cycles even at 150 degrees C. The hydrogen desorption kinetics of catalyzed and noncatalyzed MgH(2) could be understood by a modified first-order reaction model, in which the surface condition was taken into account.

  9. Decentralized and direct solar hydrogen production: Towards a hydrogen economy in MENA region

    Energy Technology Data Exchange (ETDEWEB)

    Bensebaa, Farid; Khalfallah, Mohamed; Ouchene, Majid

    2010-09-15

    Hydrogen has certainly some advantages in spite of its high cost and low efficiency when compared to other energy vectors. Solar energy is an abundant, clean and renewable source of energy, currently competing with fossil fuel for water heating without subsidy. Photo-electrochemical, thermo-chemicals and photo-biological processes for hydrogen production processes have been demonstrated. These decentralised hydrogen production processes using directly solar energy do not require expensive hydrogen infrastructure for packaging and delivery in the short and medium terms. MENA region could certainly be considered a key area for a new start to a global deployment of hydrogen economy.

  10. Nuclear Hydrogen for Peak Electricity Production and Spinning Reserve

    Energy Technology Data Exchange (ETDEWEB)

    Forsberg, C.W.

    2005-01-20

    Nuclear energy can be used to produce hydrogen. The key strategic question is this: ''What are the early markets for nuclear hydrogen?'' The answer determines (1) whether there are incentives to implement nuclear hydrogen technology today or whether the development of such a technology could be delayed by decades until a hydrogen economy has evolved, (2) the industrial partners required to develop such a technology, and (3) the technological requirements for the hydrogen production system (rate of production, steady-state or variable production, hydrogen purity, etc.). Understanding ''early'' markets for any new product is difficult because the customer may not even recognize that the product could exist. This study is an initial examination of how nuclear hydrogen could be used in two interconnected early markets: the production of electricity for peak and intermediate electrical loads and spinning reserve for the electrical grid. The study is intended to provide an initial description that can then be used to consult with potential customers (utilities, the Electric Power Research Institute, etc.) to better determine the potential real-world viability of this early market for nuclear hydrogen and provide the starting point for a more definitive assessment of the concept. If this set of applications is economically viable, it offers several unique advantages: (1) the market is approximately equivalent in size to the existing nuclear electric enterprise in the United States, (2) the entire market is within the utility industry and does not require development of an external market for hydrogen or a significant hydrogen infrastructure beyond the utility site, (3) the technology and scale match those of nuclear hydrogen production, (4) the market exists today, and (5) the market is sufficient in size to justify development of nuclear hydrogen production techniques independent of the development of any other market for hydrogen

  11. Low-Energy Catalytic Electrolysis for Simultaneous Hydrogen Evolution and Lignin Depolymerization.

    Science.gov (United States)

    Du, Xu; Liu, Wei; Zhang, Zhe; Mulyadi, Arie; Brittain, Alex; Gong, Jian; Deng, Yulin

    2017-01-19

    Here, a new proton-exchange-membrane electrolysis is presented, in which lignin was used as the hydrogen source at the anode for hydrogen production. Either polyoxometalate (POM) or FeCl3 was used as the catalyst and charge-transfer agent at the anode. Over 90 % Faraday efficiency was achieved. In a thermal-insulation reactor, the heat energy could be maintained at a very low level for continuous operation. Compared to the best alkaline-water electrolysis reported in literature, the electrical-energy consumption could be 40 % lower with lignin electrolysis. At the anode, the Kraft lignin (KL) was oxidized to aromatic chemicals by POM or FeCl3 , and reduced POM or Fe ions were regenerated during the electrolysis. Structure analysis of the residual KL indicated a reduction of the amount of hydroxyl groups and the cleavage of ether bonds. The results suggest that POM- or FeCl3 -mediated electrolysis can significantly reduce the electrolysis energy consumption in hydrogen production and, simultaneously, depolymerize lignin to low-molecular-weight value-added aromatic chemicals.

  12. Fermentation and Electrohydrogenic Approaches to Hydrogen Production (Presentation)

    Energy Technology Data Exchange (ETDEWEB)

    Maness, P. C.; Thammannagowda, S.; Magnusson, L.; Logan, B.

    2010-06-01

    This work describes the development of a waste biomass fermentation process using cellulose-degrading bacteria for hydrogen production. This process is then integrated with an electrohydrogenesis process via the development of a microbial electrolysis cell reactor, during which fermentation waste effluent is further converted to hydrogen to increase the total output of hydrogen from biomass.

  13. Hydrogen Production from Hydrogen Sulfide in IGCC Power Plants

    Energy Technology Data Exchange (ETDEWEB)

    Elias Stefanakos; Burton Krakow; Jonathan Mbah

    2007-07-31

    IGCC power plants are the cleanest coal-based power generation facilities in the world. Technical improvements are needed to help make them cost competitive. Sulfur recovery is one procedure in which improvement is possible. This project has developed and demonstrated an electrochemical process that could provide such an improvement. IGCC power plants now in operation extract the sulfur from the synthesis gas as hydrogen sulfide. In this project H{sub 2}S has been electrolyzed to yield sulfur and hydrogen (instead of sulfur and water as is the present practice). The value of the byproduct hydrogen makes this process more cost effective. The electrolysis has exploited some recent developments in solid state electrolytes. The proof of principal for the project concept has been accomplished.

  14. A New Hydrogen-Producing Strain and Its Characterization of Hydrogen Production.

    Science.gov (United States)

    Sun, Mingxing; Lv, Yongkang; Liu, Yuxiang

    2015-12-01

    A newly isolated photo non-sulfur (PNS) bacterium was identified as Rhodopseudomonas palustris PB-Z by sequencing of 16S ribosomal DNA (rDNA) genes and phylogenetic analysis. Under vigorous stirring (240 rpm), the hydrogen production performances were greatly improved: The maximum hydrogen production rate and cumulative hydrogen production increased by 188.9 ± 0.07 % and 83.0 ± 0.06 %, respectively, due to the hydrogen bubbles were immediately removed from the culture medium. The effects of different wavelength of light on hydrogen production with stirring were much different from that without stirring. The ranking on the photo-hydrogen production performance was white > yellow > green > blue > red without stirring and white > yellow > blue > red > green under stirring. The best light source for hydrogen production was tungsten filament lamp. The optimum temperature was 35 °C. The maximal hydrogen production rate and cumulative hydrogen production reached 78.7 ± 2.3 ml/l/h and 1728.1 ± 92.7 mol H2/l culture, respectively, under 35 °C, 240 rpm, and illumination of 4000 lux. Pyruvate was one of the main sources of CO2 and has a great impact on the gas composition.

  15. Superior catalytic effect of nickel ferrite nanoparticles in improving hydrogen storage properties of MgH2

    OpenAIRE

    Wan, Qi; Ping LI; Shan, Jiawei; Zhai, Fuqiang; Li, Ziliang; Qu, Xuanhui

    2015-01-01

    The catalysis of NiFe2O4 nanoparticles on the hydrogen storage performances of magnesium hydride synthesized by high-energy ball milling was studied for the first time. The H-2 storage performances and catalytic mechanism were studied by pressurecompositiontemperature (PCT), differential scanning calorimetry (DSC), X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The nonisothermal d...

  16. Solar Thermochemical Hydrogen Production Research (STCH)

    Energy Technology Data Exchange (ETDEWEB)

    Perret, Robert [Sandia National Lab. (SNL-CA), Livermore, CA (United States)

    2011-05-01

    Eight cycles in a coordinated set of projects for Solar Thermochemical Cycles for Hydrogen production (STCH) were self-evaluated for the DOE-EERE Fuel Cell Technologies Program at a Working Group Meeting on October 8 and 9, 2008. This document reports the initial selection process for development investment in STCH projects, the evaluation process meant to reduce the number of projects as a means to focus resources on development of a few most-likely-to-succeed efforts, the obstacles encountered in project inventory reduction and the outcomes of the evaluation process. Summary technical status of the projects under evaluation is reported and recommendations identified to improve future project planning and selection activities.

  17. Economical hydrogen production by electrolysis using nano pulsed DC

    Directory of Open Access Journals (Sweden)

    Dharmaraj C.H, AdishKumar S.

    2012-01-01

    Full Text Available Hydrogen is an alternate renewable eco fuel. The environmental friendly hydrogen production method is electrolysis. The cost of electrical energy input is major role while fixing hydrogen cost in the conventional direct current Electrolysis. Using nano pulse DC input make the input power less and economical hydrogen production can be established. In this investigation, a lab scale electrolytic cell developed and 0.58 mL/sec hydrogen/oxygen output is obtained using conventional and nano pulsed DC. The result shows that the nano pulsed DC gives 96.8 % energy saving.

  18. Methods and systems for the production of hydrogen

    Science.gov (United States)

    Oh, Chang H [Idaho Falls, ID; Kim, Eung S [Ammon, ID; Sherman, Steven R [Augusta, GA

    2012-03-13

    Methods and systems are disclosed for the production of hydrogen and the use of high-temperature heat sources in energy conversion. In one embodiment, a primary loop may include a nuclear reactor utilizing a molten salt or helium as a coolant. The nuclear reactor may provide heat energy to a power generation loop for production of electrical energy. For example, a supercritical carbon dioxide fluid may be heated by the nuclear reactor via the molten salt and then expanded in a turbine to drive a generator. An intermediate heat exchange loop may also be thermally coupled with the primary loop and provide heat energy to one or more hydrogen production facilities. A portion of the hydrogen produced by the hydrogen production facility may be diverted to a combustor to elevate the temperature of water being split into hydrogen and oxygen by the hydrogen production facility.

  19. Recent work in advanced hydrogen production concepts

    Science.gov (United States)

    Lawson, D. D.

    1981-03-01

    The hydrogen photoelectrolytic conversion activity investigated the practicability of semiconductor electrolytic devises that use solar energy to decompose water into hydrogen and oxygen in an apparent single step process. The photocatalytic decomposition of inorganic hydrogen compounds; i.e., hydrobromic and hydriodic acids using rhodium organic bridge complexes were also studied. The feasibility of direct high temperature thermal decompositions of water with diffusion processes for separation of the equilibrium mixture of hydrogen and oxygen into usable energy sources was examined.

  20. An Experimental Investigation of Hydrogen Production from Biomass

    Institute of Scientific and Technical Information of China (English)

    吕鹏梅; 常杰; 付严; 王铁军; 陈勇; 祝京旭

    2003-01-01

    In gaseous products of biomass steam gasification, there exist a lot of CO, CH4 and other hydrocarbons that can be converted to hydrogen through steam reforming reactions. There exists potential hydrogen production from the raw gas of biomass steam gasification. In the present work, the characteristics of hydrogen production from biomass steam gasification were investigated in a small-scale fluidized bed. In these experiments, the gasifying agent (air) was supplied into the reactor from the bottom of the reactor and the steam was added into the reactor above biomass feeding location. The effects of reaction temperature, steam to biomass ratio, equivalence ratio (ER) and biomass particle size on hydrogen yield and hydrogen yield potential were investigated. The experimental results showed that higher reactor temperature, proper ER, proper steam to biomass ratio and smaller biomass particle size will contribute to more hydrogen and potential hydrogen yield.

  1. Enhanced propylene production in FCC by novel catalytic materials

    Energy Technology Data Exchange (ETDEWEB)

    Kelkar, C.P.; Harris, D.; Xu, M.; Fu, J. [BASF Catalyst LLC, Iselin, NJ (United States)

    2007-07-01

    Fluid catalytic cracking is expected to increasingly supply the additional incremental requirements for propylene. The most efficient route to increase propylene yield from an FCC unit is through the use of medium pore zeolites such as ZSM-5. ZSM-5 zeolite cracks near linear olefins in the gasoline range to LPG olefins such as propylene and butylenes. This paper will describe catalytic approaches to increase gasoline range olefins and the chemistry of ZSM-5 to crack those olefins. The paper will also describe novel catalytic materials designed to increase propylene. (orig.)

  2. H2CAP - Hydrogen assisted catalytic biomass pyrolysis for green fuels

    DEFF Research Database (Denmark)

    Arndal, Trine Marie Hartmann; Høj, Martin; Jensen, Peter Arendt

    2014-01-01

    that can be used to upgrade the crude bio-oil to fuel-grade oil. The development of the HDO process is challenged by rapid catalyst deactivation, instability of the pyrolysis oil, poorly investigated reaction conditions and a high complexity and variability of the input oil composition. However, continuous...... catalytic hydropyrolysis coupled with downstream HDO of the pyrolysis vapors before condensation shows promise (Figure 1). A bench scale experimental setup will be constructed for the continuous conversion of solid biomass (100g /h) to low oxygen, fuel-grade bio-oil. The aim is to provide a proof......-of-concept for the proposed process(Figure 1), to understand the reaction mechanisms of HDO, to develop highly active and durable catalysts for hydropyrolysis and HDO and to optimize the operating conditions; all in order to develop a sustainable production of green transportation fuels from biomass.To support the process...

  3. Enhanced wet hydrogen peroxide catalytic oxidation performances based on CuS nanocrystals/reduced graphene oxide composites

    Science.gov (United States)

    Qian, Jing; Wang, Kun; Guan, Qingmeng; Li, Henan; Xu, Hui; Liu, Qian; Liu, Wei; Qiu, Baijing

    2014-01-01

    CuS nanocrystals/reduced graphene oxide (CuS NCs/rGO) composites were prepared by a facile one-pot solvothermal reaction. In this solvothermal system, thioacetamide was found to perform the dual roles of sulphide source and reducing agent, resulting in the formation of CuS NCs and simultaneous reduction of graphene oxide (GO) sheets to rGO sheets. In addition, CuS NCs/rGO composites were further used as heterogeneous catalysts in the wet hydrogen peroxide catalytic oxidation process, with methylene blue as a model organic dye. The introduction of rGO to CuS NCs could effectively enhance the catalytic activity of CuS NCs, and the resultant CuS NCs/rGO composites with a starting GO amount of 5 wt% showed the highest catalytic activity. Furthermore, the CuS NCs/rGO composites showed high catalytic activity over a broad pH operation range from 3.0 to 11.0 under ambient conditions, and still retained 90% of the original catalytic activity after reuse in five cycles.

  4. Decentralized production of hydrogen from hydrocarbons with reduced CO{sub 2} emission

    Energy Technology Data Exchange (ETDEWEB)

    Nazim Muradov; Franklyn Smith; Cunping Huang; Ali T-Raissi [Florida Solar Energy Center, University of Central Florida, Cocoa, Florida, (United States)

    2006-07-01

    Currently, most of the industrial hydrogen production is based on steam methane reforming process that releases significant amount of CO{sub 2} into the atmosphere. CO{sub 2} sequestration is one approach to solving the CO{sub 2} emission problem for large centralized hydrogen plants, but it would be impractical for decentralized H{sub 2} production units. The objective of this paper is to explore new routes to hydrogen production from natural gas without (or drastically reduced) CO{sub 2} emissions. One approach analyzed in this paper is based on thermo-catalytic decomposition (TCD) of hydrocarbons (e.g., methane) to hydrogen gas and elemental carbon. The paper discusses some technological aspects of the TCD process development: (1) thermodynamic analysis of TCD using AspenPlus chemical process simulator, (2) heat input options to the endothermic process, (3) catalyst activity issues, etc. Production of hydrogen and carbon via TCD of methane was experimentally verified using carbon-based catalysts. (authors)

  5. A strategy for enhancing fermentative hydrogen production from molasses

    Energy Technology Data Exchange (ETDEWEB)

    Chiu-Yue Lin; Chong-Yi Lin; Jou-Hsien Wu [Biohydrogen Lab, Graduate Institute of Civil and Hydraulic Engineering, Feng Chia University, P.O. Box 25-123, Taichung 407, Taiwan (China); Chin-Chao Chen [Department of Landscape Architecture, Chungchou Institute of Technology, Changhwa, Taiwan (China)

    2006-07-01

    This study investigated the enhancements of reactor performance by influent pretreatment for hydrogen production from molasses by a natural mixed culture enriched from sewage sludge. The reactor was operated at a temperature of 35{+-}1 C, a substrate molasses concentration of 40 g-COD/L and hydraulic retention times of 8-4 h. The thermal pretreatments on influent molasses was at 70 C for 10 min. Thermal pretreatment on the influent molasses markedly enhanced the hydrogen production and reactor performance stability. The pretreatment reactor exhibited marked increases in hydrogen content and hydrogen production rate by 40% and 35%, respectively, relative to the non-pretreatment reactor. The pretreatment reactor had hydrogen yield of 1 mmol-H{sub 2}/g-COD and specific hydrogen production rate of 6 mmol-H{sub 2}/g-VSS-day which efficiency is comparable to that of using synthetic wastewaters such as sucrose and glucose. (authors)

  6. A microBio reactor for hydrogen production.

    Energy Technology Data Exchange (ETDEWEB)

    Volponi, Joanne V.; Walker, Andrew William

    2003-12-01

    The purpose of this work was to explore the potential of developing a microfluidic reactor capable of enzymatically converting glucose and other carbohydrates to hydrogen. This aggressive project was motivated by work in enzymatic hydrogen production done by Woodward et al. at OWL. The work reported here demonstrated that hydrogen could be produced from the enzymatic oxidation of glucose. Attempts at immobilizing the enzymes resulted in reduced hydrogen production rates, probably due to buffer compatibility issues. A novel in-line sensor was also developed to monitor hydrogen production in real time at levels below 1 ppm. Finally, a theoretical design for the microfluidic reactor was developed but never produced due to the low production rates of hydrogen from the immobilized enzymes. However, this work demonstrated the potential of mimicking biological systems to create energy on the microscale.

  7. Cobalt Ferrite Nanocrystallites for Sustainable Hydrogen Production Application

    Directory of Open Access Journals (Sweden)

    Rajendra S. Gaikwad

    2011-01-01

    Full Text Available Cobalt ferrite, CoFe2O4, nanocrystalline films were deposited using electrostatic spray method and explored in sustainable hydrogen production application. Reflection planes in X-ray diffraction pattern confirm CoFe2O4 phase. The surface scanning microscopy photoimages reveal an agglomeration of closely-packed CoFe2O4 nanoflakes. Concentrated solar-panel, a two-step water splitting process, measurement technique was preferred for measuring the hydrogen generation rate. For about 5 hr sustainable, 440 mL/hr, hydrogen production activity was achieved, confirming the efficient use of cobalt ferrite nanocrystallites film in hydrogen production application.

  8. Removal of hydrogen sulfide as ammonium sulfate from hydropyrolysis product vapors

    Energy Technology Data Exchange (ETDEWEB)

    Marker, Terry L.; Felix, Larry G.; Linck, Martin B.; Roberts, Michael J.

    2017-03-14

    A system and method for processing biomass into hydrocarbon fuels that includes processing a biomass in a hydropyrolysis reactor resulting in hydrocarbon fuels and a process vapor stream and cooling the process vapor stream to a condensation temperature resulting in an aqueous stream. The aqueous stream is sent to a catalytic reactor where it is oxidized to obtain a product stream containing ammonia and ammonium sulfate. A resulting cooled product vapor stream includes non-condensable process vapors comprising H.sub.2, CH.sub.4, CO, CO.sub.2, ammonia and hydrogen sulfide.

  9. Substrate and product inhibition of hydrogen production by the extreme thermophile, Caldicellulosiruptor saccharolyticus

    NARCIS (Netherlands)

    Niel, van E.W.J.; Claassen, P.A.M.; Stams, A.J.M.

    2003-01-01

    Substrate and product inhibition of hydrogen production during sucrose fermentation by the extremely thermophilic bacterium Caldicellulosiruptor saccharolyticus was studied. The inhibition kinetics were analyzed with a noncompetitive, nonlinear inhibition model. Hydrogen was the most severe inhibito

  10. Pyranone natural products as inspirations for catalytic reaction discovery and development.

    Science.gov (United States)

    McDonald, Benjamin R; Scheidt, Karl A

    2015-04-21

    bifunctional hydrogen bonding/Brønstead base catalyst was ultimately found to enable this transformation in analogous manner to the biosynthesis via the enzyme chalcone isomerase. Employing thiourea catalysts derived from the pseudoenantiomeric quinine and quinidine, alkylidene β-ketoesters can be isomerized to 3-carboxy flavanones and decarboxylated in a single pot operation to stereodivergently provide highly enantioenriched flavanones in excellent yield. This method was applied to the synthesis of the abyssinone family of natural products, as well as the rotenoid, deguelin. An analogous method to isomerize chalcones was developed and applied to the synthesis of isosilybin A. In both of these related endeavors, the need for novel enabling methodologies toward the efficient creation of targeted molecular complexity drove the discovery, development and deployment of these stereoselective catalytic transformations.

  11. Energy Efficient Catalytic Activation of Hydrogen peroxide for Green Chemical Processes: Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Collins, Terrence J.; Horwitz, Colin

    2004-11-12

    A new, highly energy efficient approach for using catalytic oxidation chemistry in multiple fields of technology has been pursued. The new catalysts, called TAML® activators, catalyze the reactions of hydrogen peroxide and other oxidants for the exceptionally rapid decontamination of noninfectious simulants (B. atrophaeus) of anthrax spores, for the energy efficient decontamination of thiophosphate pesticides, for the facile, low temperature removal of color and organochlorines from pulp and paper mill effluent, for the bleaching of dyes from textile mill effluents, and for the removal of recalcitrant dibenzothiophene compounds from diesel and gasoline fuels. Highlights include the following: 1) A 7-log kill of Bacillus atrophaeus spores has been achieved unambiguously in water under ambient conditions within 15 minutes. 2) The rapid total degradation under ambient conditions of four thiophosphate pesticides and phosphonate degradation intermediates has been achieved on treatment with TAML/peroxide, opening up potential applications of the decontamination system for phosphonate structured chemical warfare agents, for inexpensive, easy to perform degradation of stored and aged pesticide stocks (especially in Africa and Asia), for remediation of polluted sites and water bodies, and for the destruction of chemical warfare agent stockpiles. 3) A mill trial conducted in a Pennsylvanian bleached kraft pulp mill has established that TAML catalyst injected into an alkaline peroxide bleach tower can significantly lower color from the effluent stream promising a new, more cost effective, energy-saving approach for color remediation adding further evidence of the value and diverse engineering capacity of the approach to other field trials conducted on effluent streams as they exit the bleach plant. 4) Dibenzothiophenes (DBTs), including 4,6-dimethyldibenzothiophene, the most recalcitrant sulfur compounds in diesel and gasoline, can be completely removed from model gasoline

  12. Hydrogen production from water: Recent advances in photosynthesis research

    Energy Technology Data Exchange (ETDEWEB)

    Greenbaum, E.; Lee, J.W. [Oak Ridge National Lab., TN (United States). Chemical Technology Div.

    1997-12-31

    The great potential of hydrogen production by microalgal water splitting is predicated on quantitative measurement of the algae`s hydrogen-producing capability, which is based on the following: (1) the photosynthetic unit size of hydrogen production; (2) the turnover time of photosynthetic hydrogen production; (3) thermodynamic efficiencies of conversion of light energy into the Gibbs free energy of molecular hydrogen; (4) photosynthetic hydrogen production from sea water using marine algae; (5) the potential for research advances using modern methods of molecular biology and genetic engineering to maximize hydrogen production. ORNL has shown that sustained simultaneous photoevolution of molecular hydrogen and oxygen can be performed with mutants of the green alga Chlamydomonas reinhardtii that lack a detectable level of the Photosystem I light reaction. This result is surprising in view of the standard two-light reaction model of photosynthesis and has interesting scientific and technological implications. This ORNL discovery also has potentially important implications for maximum thermodynamic conversion efficiency of light energy into chemical energy by green plant photosynthesis. Hydrogen production performed by a single light reaction, as opposed to two, implies a doubling of the theoretically maximum thermodynamic conversion efficiency from {approx}10% to {approx}20%.

  13. Principle and perspectives of hydrogen production through biocatalyzed electrolysis

    NARCIS (Netherlands)

    Rozendal, R.A.; Hamelers, H.V.M.; Euverink, G.J.W.; Metz, S.J.; Buisman, C.J.N.

    2006-01-01

    Biocatalyzed electrolysis is a novel biological hydrogen production process with the potential to efficiently convert a wide range of dissolved organic materials in wastewaters. Even substrates formerly regarded to be unsuitable for hydrogen production due to the endothermic nature of the involved c

  14. Maximizing Light Utilization Efficiency and Hydrogen Production in Microalgal Cultures

    Energy Technology Data Exchange (ETDEWEB)

    Melis, Anastasios [Univ. of California, Berkeley, CA (United States)

    2014-12-31

    The project addressed the following technical barrier from the Biological Hydrogen Production section of the Fuel Cell Technologies Program Multi-Year Research, Development and Demonstration Plan: Low Sunlight Utilization Efficiency in Photobiological Hydrogen Production is due to a Large Photosystem Chlorophyll Antenna Size in Photosynthetic Microorganisms (Barrier AN: Light Utilization Efficiency).

  15. Solar and Wind Technologies for Hydrogen Production Report to Congress

    Energy Technology Data Exchange (ETDEWEB)

    None, None

    2005-12-01

    DOE's Solar and Wind Technologies for Hydrogen Production Report to Congress summarizes the technology roadmaps for solar- and wind-based hydrogen production. Published in December 2005, it fulfills the requirement under section 812 of the Energy Policy Act of 2005.

  16. Life cycle assessment of processes for hydrogen production. Environmental feasibility and reduction of greenhouse gases emissions

    Energy Technology Data Exchange (ETDEWEB)

    Dufour, J.; Moreno, J. [Department of Chemical and Environmental Technology, ESCET, Universidad Rey Juan Carlos, c/Tulipan s/n, 28933 Mostoles, Madrid (Spain); Serrano, D.P. [Department of Chemical and Environmental Technology, ESCET, Universidad Rey Juan Carlos, c/Tulipan s/n, 28933 Mostoles, Madrid (Spain)]|[IMDEA Energia, c/Tulipan s/n, 28933 Mostoles, Madrid (Spain); Galvez, J.L.; Garcia, C. [National Institute of Aerospace Technology (INTA), Renewable Energies Area, Crtra. Ajalvir Km 4, 28850 Torrejon de Ardoz, Madrid (Spain)

    2009-02-15

    Decomposition of CH{sub 4} (natural gas) is one of the alternatives under study to achieve the sustainable production of hydrogen. No CO{sub 2} or other greenhouse gases emissions are produced in this route and carbon is obtained as a solid co-product at the end of the reaction (CH{sub 4}<-> C+2 H{sub 2}). This process can be thermally or catalytically conducted and recent studies have demonstrated that the carbon obtained in the reaction can also show catalytic activity. In this work, thermal and autocatalytic decomposition of methane were studied and compared with the steam reforming with and without CO{sub 2} capture and storage from an environmental point of view, using life cycle assessment (LCA) tools. As well, different energetic scenarios were included in the study. The selected functional unit was 1 Nm{sup 3} of hydrogen and the LCA was focused on material and raw materials acquisition and manufacturing stages. The assessment was carried out with SimaPro 7.1 software by using Eco-indicator 95 method. Results showed that autocatalytic decomposition is the most environmental-friendly process for hydrogen production since presented the lowest total environmental impact and CO{sub 2} emissions. Also, steam reforming with CO{sub 2} capture and storage led to lower CO{sub 2} emissions but higher total environmental impact than conventional steam reforming. (author)

  17. Fluid-Bed Testing of Greatpoint Energy's Direct Oxygen Injection Catalytic Gasification Process for Synthetic Natural Gas and Hydrogen Coproduction Year 6 - Activity 1.14 - Development of a National Center for Hydrogen Technology

    Energy Technology Data Exchange (ETDEWEB)

    Swanson, Michael; Henderson, Ann

    2012-04-01

    The GreatPoint Energy (GPE) concept for producing synthetic natural gas and hydrogen from coal involves the catalytic gasification of coal and carbon. GPE’s technology “refines” coal by employing a novel catalyst to “crack” the carbon bonds and transform the coal into cleanburning methane (natural gas) and hydrogen. The GPE mild “catalytic” gasifier design and operating conditions result in reactor components that are less expensive and produce pipeline-grade methane and relatively high purity hydrogen. The system operates extremely efficiently on very low cost carbon sources such as lignites, subbituminous coals, tar sands, petcoke, and petroleum residual oil. In addition, GPE’s catalytic coal gasification process eliminates troublesome ash removal and slagging problems, reduces maintenance requirements, and increases thermal efficiency, significantly reducing the size of the air separation plant (a system that alone accounts for 20% of the capital cost of most gasification systems) in the catalytic gasification process. Energy & Environmental Research Center (EERC) pilot-scale gasification facilities were used to demonstrate how coal and catalyst are fed into a fluid-bed reactor with pressurized steam and a small amount of oxygen to “fluidize” the mixture and ensure constant contact between the catalyst and the carbon particles. In this environment, the catalyst facilitates multiple chemical reactions between the carbon and the steam on the surface of the coal. These reactions generate a mixture of predominantly methane, hydrogen, and carbon dioxide. Product gases from the process are sent to a gas-cleaning system where CO{sub 2} and other contaminants are removed. In a full-scale system, catalyst would be recovered from the bottom of the gasifier and recycled back into the fluid-bed reactor. The by-products (such as sulfur, nitrogen, and CO{sub 2}) would be captured and could be sold to the chemicals and petroleum industries, resulting in

  18. A review of recent advances on the effects of microstructural refinement and nano-catalytic additives on the hydrogen storage properties of metal and complex hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Varin, R. A.; Zbroniec, L. [University of Waterloo, Department of Mechanical and Mechatronics Engineering, Waterloo, Ontario (Canada); Polanski, M.; Bystrzycki, J. [Faculty of Advanced Technology and Chemistry, Military University of Technology, Warsaw (Poland)

    2011-07-01

    The recent advances on the effects of microstructural refinement and various nano-catalytic additives on the hydrogen storage properties of metal and complex hydrides obtained in the last few years in the allied laboratories at the University of Waterloo (Canada) and Military University of Technology (Warsaw, Poland) are critically reviewed in this paper. The research results indicate that microstructural refinement (particle and grain size) induced by ball milling influences quite modestly the hydrogen storage properties of simple metal and complex metal hydrides. On the other hand, the addition of nanometric elemental metals acting as potent catalysts and/or metal halide catalytic precursors brings about profound improvements in the hydrogen absorption/desorption kinetics for simple metal and complex metal hydrides alike. In general, catalytic precursors react with the hydride matrix forming a metal salt and free nanometric or amorphous elemental metals/intermetallics which, in turn, act catalytically. However, these catalysts change only kinetic properties i.e. the hydrogen absorption/desorption rate but they do not change thermodynamics (e.g., enthalpy change of hydrogen sorption reactions). It is shown that a complex metal hydride, LiAlH{sub 4}, after high energy ball milling with a nanometric Ni metal catalyst and/or MnCl{sub 2} catalytic precursor, is able to desorb relatively large quantities of hydrogen at room temperature, 40 and 80 {sup o}C. This kind of behavior is very encouraging for the future development of solid state hydrogen systems. (authors)

  19. A Review of Recent Advances on the Effects of Microstructural Refinement and Nano-Catalytic Additives on the Hydrogen Storage Properties of Metal and Complex Hydrides

    Directory of Open Access Journals (Sweden)

    Jerzy Bystrzycki

    2010-12-01

    Full Text Available The recent advances on the effects of microstructural refinement and various nano-catalytic additives on the hydrogen storage properties of metal and complex hydrides obtained in the last few years in the allied laboratories at the University of Waterloo (Canada and Military University of Technology (Warsaw, Poland are critically reviewed in this paper. The research results indicate that microstructural refinement (particle and grain size induced by ball milling influences quite modestly the hydrogen storage properties of simple metal and complex metal hydrides. On the other hand, the addition of nanometric elemental metals acting as potent catalysts and/or metal halide catalytic precursors brings about profound improvements in the hydrogen absorption/desorption kinetics for simple metal and complex metal hydrides alike. In general, catalytic precursors react with the hydride matrix forming a metal salt and free nanometric or amorphous elemental metals/intermetallics which, in turn, act catalytically. However, these catalysts change only kinetic properties i.e. the hydrogen absorption/desorption rate but they do not change thermodynamics (e.g., enthalpy change of hydrogen sorption reactions. It is shown that a complex metal hydride, LiAlH4, after high energy ball milling with a nanometric Ni metal catalyst and/or MnCl2 catalytic precursor, is able to desorb relatively large quantities of hydrogen at RT, 40 and 80 °C. This kind of behavior is very encouraging for the future development of solid state hydrogen systems.

  20. Partial Characteristics of Hydrogen Production by Fermentative Hydrogen-producing Bacterial Strain B49

    Institute of Scientific and Technical Information of China (English)

    Wang Xiangjing(王相晶); Ren Nanqi; Xiang Wensheng; Lin Ming; Guo Wanqian

    2003-01-01

    To investigate the characteristics of hydrogen production by a novel fermentative hydrogen-producing bacterial strain B49 (AF481148 in EMBL), batch experiments are conducted under different conditions. Hydrogen production has a correlation with cell growth and the consumption of glucose and soluble protein. The optimum pH for cell growth is 4.5±0.15. At acidic pH 4.0±0.15, the bacteria has the maximum accumulated hydrogen volume of 2382 ml/L culture and the maximum hydrogen evolution rate of 339.9 ml/L culture*h with 1% glucose. The optimum temperature for cell growth and hydrogen production is 35℃. In addition, fermentative hydrogen-producing bacterial strain B49 can generate hydrogen from the decomposition of other organic substrates such as wheat, soybean, corn, and potato. Moreover, it can also produce hydrogen from molasses wastewater and brewage wastewater, and hydrogen yields are 137.9 ml H2/g COD and 49.9 ml H2/g COD, respectively.

  1. Catalytic performance of Fe modified K/Mo2C catalyst for CO hydrogenation

    Institute of Scientific and Technical Information of China (English)

    Minglin Xiang; Dudu Wu; Juan Zou; Debao Li; Yuhan Sun; Xichun She

    2011-01-01

    Fe modified and un-modified K/Mo2C were prepared and investigated as catalysts for CO hydrogenation reaction.Compared with K/Mo2C catalyst,the addition of Fe increased the production of alcohols,especially the C2+OH.Meanwhile,considerable amounts of C5+ hydrocarbons and C=2-C=4 were formed,whereas methane selectivity greatly decreased.Also,the activity and selectivity of the catalyst were readily affected by the reaction pressure and temperature employed.According to the XPS results,Mo4+ might be responsible for the production of alcohols,whereas the low valence state of Mo species such as Moo and/or Mo2+ might be account for the high activity and selectivity toward hydrocarbons.

  2. Effect of Co crystallinity on Co/CNT catalytic activity in CO/CO{sub 2} hydrogenation and CO disproportionation

    Energy Technology Data Exchange (ETDEWEB)

    Chernyak, Sergei A., E-mail: chernyak.msu@gmail.com [Lomonosov Moscow State University, Department of Chemistry, Leninskiye Gory 1-3, Moscow 119991 (Russian Federation); Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, Department of Physical Chemistry, Leninsky Avenue 31, Moscow 119991 (Russian Federation); Suslova, Evgeniya V.; Egorov, Alexander V.; Maslakov, Konstantin I. [Lomonosov Moscow State University, Department of Chemistry, Leninskiye Gory 1-3, Moscow 119991 (Russian Federation); Savilov, Serguei V.; Lunin, Valery V. [Lomonosov Moscow State University, Department of Chemistry, Leninskiye Gory 1-3, Moscow 119991 (Russian Federation); Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, Department of Physical Chemistry, Leninsky Avenue 31, Moscow 119991 (Russian Federation)

    2016-05-30

    Highlights: • Amorphous and crystalline Co supported on CNTs were obtained by tuning of CNT surface. • CO and CO{sub 2} hydrogenation does not occur on amorphous Co particles. • Thermal activation of amorphous Co led to crystallization of metal. • Amorphous Co promotes CO disproportionation. • Carbon shells around the amorphous metal particles after the CO hydrogenation. - Abstract: Carbon nanotubes (CNTs) with different degree of surface oxidation were used as supports for 5 wt.% Co catalysts. CNTs and Co/CNT catalysts were analyzed by XPS, nitrogen adsorption, TEM and electron diffraction to reveal their structure. High oxidation degree of CNT surface (8.6 at.% of O) and low Co loading led to predominantly amorphous Co species. This resulted in the absence of catalytic activity in both CO and CO{sub 2} hydrogenation in opposite to the catalyst supported on less oxidized CNTs (5.4 at.% of O) where Co species were found to be crystalline. Thermal treatment of inactive catalyst in H{sub 2} and He led to the formation of Co crystal phase which was active in catalysis. Co particle size in catalyst supported on strongly oxidized CNTs was unchanged during CO hydrogenation in opposite to Co supported on less oxidized CNTs. Carbon shell formation on the surface of amorphous Co particles during CO hydrogenation was revealed, which testified CO disproportionation. Qualitative mechanism of CO hydrogenation on small Co particles was proposed.

  3. Research Progress in Catalytic Hydrogenation of CO2 to Ethanol%CO2催化加氢制乙醇研究进展

    Institute of Scientific and Technical Information of China (English)

    王慧敏; 杨绪壮; 张兵兵; 苏海全

    2012-01-01

    燃料乙醇是可再生的清洁燃料,具有替代汽油的应用前景.以CO2气体为碳源并通过催化加氢制燃料乙醇具有环境保护和节约能源的现实意义.主要介绍了CO2催化加氢的反应机理以及催化剂活性组分、前驱物、助剂及载体对催化活性、产物选择性的影响,同时介绍了反应条件对催化过程的影响.%Fuel ethanol is often regarded as a potential renewable clean alternative fuel to gasoline. It has practical significance of environmental protection and energy conservation to synthesize fuel ethanol by the hydrogenation of CO2. The reaction mechanism of catalytic hydrogenation of CO2 to ethanol as well as the effects of active sites,precursors,promoters and supports on the catalytic activity and product selectivity are reviewed. Moreover,the effects of reaction conditions on the catalysis are also introduced.

  4. Selecting effective hydrogen production and delivery options for mining applications

    Energy Technology Data Exchange (ETDEWEB)

    Curran, K.M. [Air Liquide Canada Inc., Ottawa, ON (Canada)

    2007-11-15

    This paper explored solutions to the challenges facing underground mining operations with respect to diesel powered equipment that results in increased ventilation requirements. The use of hydrogen as a fuel offers benefits in the area of reduced particulate and toxic emissions when it is used both in an internal combustion engine and when the energy of hydrogen is converted to electricity via a fuel cell. This paper examined the economics associated with 4 portions of the hydrogen supply chain for 3 commercially available methods for hydrogen supply. The 4 elements of each supply chain were production, distribution, storage and dispensing. The 3 methods for supply included gaseous product delivered by tube trailers; gaseous hydrogen onsite production through electrolysis; and, liquid hydrogen delivery. The choice of hydrogen supply mode was shown to be a complex process that must take into account all elements of the supply chain in terms of the end user defined by flow rate, pressure and purity. The cost of energy must also be considered, both for onsite production and for the transport cost of any delivered product. It was concluded that gaseous hydrogen offers flexibility in lower flow situations while liquid hydrogen offers the most economic supply method when distance from the liquid source is manageable by bulk tanker. 14 figs.

  5. Steam reforming of natural gas with integrated hydrogen separation for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Oertel, M.; Schmitz, J.; Weirich, W.; Jendryssek-Neumann, D.; Schulten, R.

    1987-08-01

    The development of heat resistant permeation membranes has opened up new possibilities for the conversion of fossil energy resources. In steam reforming of natural gas, such membranes even permit a direct production of hydrogen at high temperatures during the conversion of feed hydrocarbons. Further gas processing, such as required for reformer gas in existing hydrogen production processes, is not necessary. Due to continuous hydrogen discharge directly in the reformer tube, the chemical equilibrium of the occurring reactions becomes displaced towards the products, resulting in more favourable process conditions and, consequently, in improved by 36% utilization of the feed hydrocarbons. At the same time, the hydrogen yield increases by 44%. The heat required, which is provided by a high temperature reactor, is 17% in excess of that in conventional plants. It can be expected that the simplified process design will produce substantial cost advantages over the existing processes for the production of hydrogen.

  6. Fermentative hydrogen production by microbial consortium

    Energy Technology Data Exchange (ETDEWEB)

    Maintinguer, Sandra I.; Fernandes, Bruna S.; Duarte, Iolanda C.S.; Saavedra, Nora Katia; Adorno, M. Angela T.; Varesche, M. Bernadete [Department of Hydraulics and Sanitation, School of Engineering of Sao Carlos, University of Sao Paulo, Av. Trabalhador Sao-carlense, 400, 13566-590 Sao Carlos-SP (Brazil)

    2008-08-15

    Heat pre-treatment of the inoculum associated to the pH control was applied to select hydrogen-producing bacteria and endospores-forming bacteria. The source of inoculum to the heat pre-treatment was from a UASB reactor used in the slaughterhouse waste treatment. The molecular biology analyses indicated that the microbial consortium presented microorganisms affiliated with Enterobacter cloacae (97% and 98%), Clostridium sp. (98%) and Clostridium acetobutyricum (96%), recognized as H{sub 2} and volatile acids' producers. The following assays were carried out in batch reactors in order to verify the efficiencies of sucrose conversion to H{sub 2} by the microbial consortium: (1) 630.0 mg sucrose/L, (2) 1184.0 mg sucrose/L, (3) 1816.0 mg sucrose/L and (4) 4128.0 mg sucrose/L. The subsequent yields were obtained as follows: 15% (1.2 mol H{sub 2}/mol sucrose), 20% (1.6 mol H{sub 2}/mol sucrose), 15% (1.2 mol H{sub 2}/mol sucrose) and 4% (0.3 mol H{sub 2}/mol sucrose), respectively. The intermediary products were acetic acid, butyric acid, methanol and ethanol in all of the anaerobic reactors. (author)

  7. Open-loop thermochemical cycles for the production of hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Conger, W.L.

    1979-01-01

    The concept of open-loop thermochemical cycles (cycles which have additional or other feedstocks than water and produce materials in addition to hydrogen and oxygen) is introduced. Preliminary analysis of possible feedstocks available indicates substantial quantities of hydrogen could possibly be produced through open-cycles. The advantages of open-cycles include the conversion of unwanted waste products to useful products while producing hydrogen. A compilation of open processes which would have SO/sub 2/ in addition to water as feedstock and which would produce sulfuric acid in addition to hydrogen and oxygen is given.

  8. Hydrogen Production Cost Estimate Using Biomass Gasification: Independent Review

    Energy Technology Data Exchange (ETDEWEB)

    none,

    2011-10-01

    This independent review is the conclusion arrived at from data collection, document reviews, interviews and deliberation from December 2010 through April 2011 and the technical potential of Hydrogen Production Cost Estimate Using Biomass Gasification. The Panel reviewed the current H2A case (Version 2.12, Case 01D) for hydrogen production via biomass gasification and identified four principal components of hydrogen levelized cost: CapEx; feedstock costs; project financing structure; efficiency/hydrogen yield. The panel reexamined the assumptions around these components and arrived at new estimates and approaches that better reflect the current technology and business environments.

  9. Electrolytic production of hydrogen utilizing photovoltaic cells

    Energy Technology Data Exchange (ETDEWEB)

    Daugherty, M.A.

    1996-10-01

    Hydrogen has the potential to serve as both an energy storage means and an energy carrier in renewable energy systems. When renewable energy sources such as solar or wind power are used to produce electrical power, the output can vary depending on weather conditions. By using renewable sources to produce hydrogen, a fuel which can be stored and transported, a reliable and continuously available energy supply with a predictable long-term average output is created. Electrolysis is one method of converting renewable energy into hydrogen fuel. In this experiment we examine the use of an electrolyzer based on polymer-electrolyte membrane technology to separate water into hydrogen and oxygen. The oxygen is vented to the atmosphere and the hydrogen is stored in a small pressure vessel.

  10. The endogenous production of hydrogen sulphide in intrauterine tissues

    Directory of Open Access Journals (Sweden)

    Wang Rui

    2009-02-01

    Full Text Available Abstract Background Hydrogen sulphide is a gas signalling molecule which is produced endogenously from L-cysteine via the enzymes cystathionine beta-synthase (CBS and cystathionine gamma-lyase (CSE. The possible role of hydrogen sulphide in reproduction has not yet been fully investigated. It has been previously demonstrated that hydrogen sulphide relaxes uterine smooth muscle in vitro. The aim of the present study was to investigate the endogenous production of hydrogen sulphide in rat and human intrauterine tissues in vitro. Methods The production of hydrogen sulphide in rat and human intrauterine tissues was measured in vitro using a standard technique. The expression of CBS and CSE was also investigated in rat and human intrauterine tissues via Western blotting. Furthermore, the effects of nitric oxide (NO and low oxygen conditions on the production rates of hydrogen sulphide were investigated. Results The order of hydrogen sulphide production rates (mean +/- SD, n = 4 for rat tissues were: liver (777 +/- 163 nM/min/g > uterus (168 +/- 100 nM/min/g > fetal membranes (22.3 +/- 15.0 nM/min/g > placenta (11.1 +/- 4.7 nM/min/g, compared to human placenta (200 +/- 102 nM/min/g. NO significantly increased hydrogen sulphide production in rat fetal membranes (P Conclusion Rat and human intrauterine tissues produce hydrogen sulphide in vitro possibly via CBS and CSE enzymes. NO increased the production of hydrogen sulphide in rat fetal membranes. The augmentation of hydrogen sulphide production in human intrauterine tissues in a low oxygen environment could have a role in pathophysiology of pregnancy.

  11. Photoelectrochemical hydrogen production from biomass derivatives and water.

    Science.gov (United States)

    Lu, Xihong; Xie, Shilei; Yang, Hao; Tong, Yexiang; Ji, Hongbing

    2014-11-21

    Hydrogen, a clean energy carrier with high energy capacity, is a very promising candidate as a primary energy source for the future. Photoelectrochemical (PEC) hydrogen production from renewable biomass derivatives and water is one of the most promising approaches to producing green chemical fuel. Compared to water splitting, hydrogen production from renewable biomass derivatives and water through a PEC process is more efficient from the viewpoint of thermodynamics. Additionally, the carbon dioxide formed can be re-transformed into carbohydrates via photosynthesis in plants. In this review, we focus on the development of photoanodes and systems for PEC hydrogen production from water and renewable biomass derivatives, such as methanol, ethanol, glycerol and sugars. We also discuss the future challenges and opportunities for the design of the state-of-the-art photoanodes and PEC systems for hydrogen production from biomass derivatives and water.

  12. Catalytic Production of Ethanol from Biomass-Derived Synthesis Gas

    Energy Technology Data Exchange (ETDEWEB)

    Trewyn, Brian G. [Colorado School of Mines, Golden, CO (United States); Smith, Ryan G. [Iowa State Univ., Ames, IA (United States)

    2016-06-01

    Heterogeneous catalysts have been developed for the conversion of biomass-derived synthetic gas (syngas) to ethanol. The objectives of this project were to develop a clean synthesis gas from biomass and develop robust catalysts with high selectivity and lifetime for C2 oxygenate production from biomass-derived syngas and surrogate syngas. During the timeframe for this project, we have made research progress on the four tasks: (1) Produce clean bio-oil generated from biomass, such as corn stover or switchgrass, by using fast pyrolysis system, (2) Produce clean, high pressure synthetic gas (syngas: carbon monoxide, CO, and hydrogen, H2) from bio-oil generated from biomass by gasification, (3) Develop and characterize mesoporous mixed oxide-supported metal catalysts for the selective production of ethanol and other alcohols, such as butanol, from synthesis gas, and (4) Design and build a laboratory scale synthesis gas to ethanol reactor system evaluation of the process. In this final report, detailed explanations of the research challenges associated with this project are given. Progress of the syngas production from various biomass feedstocks and catalyst synthesis for upgrading the syngas to C2-oxygenates is included. Reaction properties of the catalyst systems under different reaction conditions and different reactor set-ups are also presented and discussed. Specifically, the development and application of mesoporous silica and mesoporous carbon supports with rhodium nanoparticle catalysts and rhodium nanoparticle with manganese catalysts are described along with the significant material characterizations we completed. In addition to the synthesis and characterization, we described the activity and selectivity of catalysts in our micro-tubular reactor (small scale) and fixed bed reactor (larger scale). After years of hard work, we are proud of the work done on this project, and do believe that this work will provide a solid

  13. Hydrogen production by fermentation using acetic acid and lactic acid.

    Science.gov (United States)

    Matsumoto, Mitsufumi; Nishimura, Yasuhiko

    2007-03-01

    Microbial hydrogen production from sho-chu post-distillation slurry solution (slurry solution) containing large amounts of organic acids was investigated. The highest hydrogen producer, Clostridium diolis JPCC H-3, was isolated from natural environment and produced hydrogen at 6.03+/-0.15 ml from 5 ml slurry solution in 30 h. Interestingly, the concentration of acetic acid and lactic acid in the slurry solution decreased during hydrogen production. The substrates for hydrogen production by C. diolis JPCC H-3, in particular organic acids, were investigated in an artificial medium. No hydrogen was produced from acetic acid, propionic acid, succinic acid, or citric acid on their own. Hydrogen and butyric acid were produced from a mixture of acetic acid and lactic acid, showing that C. diolis. JPCC H-3 could produce hydrogen from acetic acid and lactic acid. Furthermore, calculation of the Gibbs free energy strongly suggests that this reaction would proceed. In this paper, we describe for the first time microbial hydrogen production from acetic acid and lactic acid by fermentation.

  14. Fermentative hydrogen production from xylose using anaerobic mixed microflora

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Chiu-Yue; Cheng, Chao-Hui [BioHydrogen Laboratory, Department of Hydraulic Engineering, Feng Chia University, P.O. Box 25-123, Taichung 40724 (Taiwan)

    2006-06-15

    Sewage sludge microflora were anaerobically cultivated in a chemostat-type anaerobic bioreactor at a temperature of 35+/-1{sup o}C, pH of 7.1 and hydraulic retention time of 12h to determine the hydrogen production efficiency from xylose (20g-COD/L). This enriched microflora was used as a seed in batch experiments to investigate the pH and substrate concentration effects on hydrogen-producing bioactivity. It is demonstrated that the enriched mesophilic sewage sludge microflora with a continuous feeding can produce hydrogen from xylose with hydrogen content of 32% (v/v) in the biogas. Each mole of xylose yields 0.7moles of hydrogen and each gram of biomass produces 0.038moles of hydrogen per day. According to the batch test results, changes in pH and xylose concentration could enhance the microflora hydrogen production activity. Batch cultivation of this mixed microflora at pH values of 6-7 and xylose concentrations of 20g-COD/L resulted in high hydrogen production with a yield of 1.92-2.25mol-H{sub 2}/mol-xylose. This value is comparable to that from an enrichment culture. Strategies based on pH and xylose concentration controls for optimal hydrogen production from xylose using sewage sludge microflora are proposed. (author)

  15. Hydrogen production by Rhodobacter sphaeroides DSM 158 under intense irradiation.

    Science.gov (United States)

    Krujatz, Felix; Härtel, Paul; Helbig, Karsten; Haufe, Nora; Thierfelder, Simone; Bley, Thomas; Weber, Jost

    2015-01-01

    To identify optimal hydrogen production conditions using growing cultures of Rhodobacter sphaeroides DSM 158 the effects of varying the reactor's volumetric power input (0.01-1.4kWm(-3)) and irradiation intensity (5-2500Wm(-2)) were investigated in batch and continuous production modes. Irradiation intensity had a greater effect on hydrogen production than volumetric power input. Hydrogen production and photofermentative biomass formation were maximized by irradiation at 2250Wm(-2) with a volumetric power input of 0.55kWm(-3). The bacterial dry weight (2.64gL(-1)) and rate of hydrogen production (195mLL(-1)h(-1)) achieved under these conditions were greater than any that have previously been reported for batch-mode hydrogen production by R. sphaeroides. Continuous mode experiments (D=0.1h(-1)) yielded a bacterial dry weight, hydrogen production rate, productivity and hydrogen yield of 2.35±0.18gL(-1), 165±6.2mLL(-1)h(-1), 3.96LL(-1)d(-1) and 36.6%, respectively.

  16. Comparative analysis of hydrogen-producing bacteria and its immobilized cells for characteristics of hydrogen production

    Institute of Scientific and Technical Information of China (English)

    王相晶; 任南琪; 向文胜; 王爱杰; 林明; 郭婉茜

    2003-01-01

    A strain of hydrogen producing bacteria was immobilized by polyvinyl alcohol-boric acid method,with the addition of a small amount of calcium alginate. The immobilized cells were insensitive to the presence of traces of O2. Moreover, the immobilized cells increased both the evolution rate and the yield of hydrogen production. Batch experiments with a medium containing 10 g/L glucose demonstrated the yields of hydrogen production by the immobilized and free cells were 2.14 mol/mol glucose and 1.69 mol/mol glucose, respectively.In continuous cultures atmedium retention time of 2. 0 h, the yield and the evolution rate of hydrogen producmedium retention time of 6. 0 h, the yield and the evolution rate of hydrogen production by free cells were only 1.75 mol/mol glucose and 362.9ml/(L·h),respectively.

  17. Selective catalytic methanation of CO in hydrogen-rich gases over Ni/ZrO2 catalyst

    Institute of Scientific and Technical Information of China (English)

    Qihai Liu; Xinfa Dong; Xinman Mo; Weiming Lin

    2008-01-01

    Ni/ZrO2 catalysts were prepared by the incipient-wetness impregnation method and were investigated in activity and selectivity for the selective catalytic methanation of CO in hydrogen-rich gases with more than 20 vol%CO2.The result showed that Ni loadings significantly influenced the performance of Ni/ZrO2 catalyst.The 1.6 wt%Ni loading catalyst exhibited the highest catalytic activity among all the catalysts in the selective methanation of CO in hydrogen-rich gas.The outlet concentration of CO was less than 20 ppm with the hydrogen consumption below 7%.at a gas-hourly-space velocity as high as 10000 h-1 and a temperature range of 260℃ to 280℃.The X-ray diffraction(XRD)and temperature programmed reduction (TPR)measurements showed that NiO was dispersed thoroughly on the surface of ZrO2 support if Ni loading was under 1.6 wt%.When N-10ading was increased to 3 wt%or above.the free bulk NiO species began to assemble,which was not favorable to increase the selectivity of the catalyst.

  18. Microbiological Hydrogen Production by Anaerobic Fermentation and Photosynthetic Process

    Energy Technology Data Exchange (ETDEWEB)

    Asada, Y.; Ohsawa, M.; Nagai, Y.; Fukatsu, M.; Ishimi, K.; Ichi-ishi, S.

    2009-07-01

    Hydrogen gas is a clean and renewable energy carrier. Microbiological hydrogen production from glucose or starch by combination used of an anaerobic fermenter and a photosynthetic bacterium, Rhodobacter spheroides RV was studied. In 1984, the co-culture of Clostridium butyricum and RV strain to convert glucose to hydrogen was demonstrated by Miyake et al. Recently, we studied anaerobic fermentation of starch by a thermophilic archaea. (Author)

  19. New nanosized catalytic membrane reactors for hydrogenation with stored hydrogen: Prerequisites and the experimental basis for their creation

    Science.gov (United States)

    Soldatov, A. P.; Tsodikov, M. V.; Parenago, O. P.; Teplyakov, V. V.

    2010-12-01

    The prerequisites and prospects for creating a new generation of nanosized membrane reactors are considered. For the first time, hydrogenation reactions take place in ceramic membrane pores with hydrogen adsorbed beforehand in mono- and multilayered oriented carbon nanotubes with graphene walls (OCNTGs) formed on the internal pore surface. It is shown for Trumem microfiltration membranes with D avg ˜130 nm that oxidation reactions of CO on a Cu0.03Ti0.97O2 ± δ catalyst and the oxidative conversion of methane into synthesis gas and light hydrocarbons on La + Ce/MgO are considerably enhanced when they occur in membranes. Regularities of hydrogen adsorption, storage, and desorption in nanosized membrane reactors are investigated through OCNTG formation in Trumem ultrafiltration membrane pores with D avg = 50 and 90 nm and their saturation with hydrogen at a pressure of 10-13 MPa. It is shown that the amount of adsorbed hydrogen reaches 14.0% of OCNTG mass. Using thermogravimetric analysis in combination with mass-spectrometric analysis, hydrogen adsorption in OCNTG is first determined and its desorption is found to proceed at atmospheric pressure at a temperature of ˜175°C. It is shown that adsorbed hydrogen affects the transport properties of the membranes, reducing their efficiency with respect to liquids by 4-26 times. This is indirect confirmation of its high activity, due apparently the dissociative mechanism of adsorption.

  20. Catalytic combustion in environmental protection and energy production

    Energy Technology Data Exchange (ETDEWEB)

    Ahlstroem-Silversand, F.

    1996-12-01

    This thesis is focused on three different areas of catalytic combustion: -Catalytic combustion of diesel soot, -Development of catalytically active wire meshes through thermal spraying, -Stabilisation and activation of {gamma}-alumina for methane combustion. Emissions of diesel soot may be trapped and combusted in a particulate trap coated with catalytically active materials. The soot particles must be combusted at temperatures prevailing in diesel exhausts, generally between 150 and 400 deg C. To facilitate effective combustion at these temperatures, the particulate trap should be coated with an oxide catalyst consisting of V{sub 2}O{sub 5}/CuO (V:Cu=0.9 on molar basis). Catalytically active wire meshes offer a number of advantages over pellets and monolith catalysts. They combine geometric flexibility with excellent mass- and heat- transfer characteristics and a low pressure drop. By using a modified thermal spray technique, it is possible to produce porous adhesive ceramic coatings on metal surfaces. The specific surface area can be increased through deposition of a high-surface-area material into the macro-porosity of the as-sprayed layer. The ceramic layer is finally activated through a conventional impregnation technique. Palladium dispersed onto a Si-stabilised {gamma}-alumina is an appropriate combustion catalyst at temperatures below 1000 deg C. Adding small amounts of rhodium or platinum to the palladium increases the catalyst activity but decreases the catalyst`s stability to thermal deactivation. The addition of rare-earth-metal oxides will lead to increased thermal stability but to a decreased activity. Long-term deactivation tests show that the activity for combustion of methane decreases to the same extent as the value of the specific surface area, thus indicating that the alumina surface may play an important role during the activation of adsorbed methane molecules. 29 refs, 14 figs

  1. Hydrogen production from dimethyl ether using corona discharge plasma

    Science.gov (United States)

    Zou, Ji-Jun; Zhang, Yue-Ping; Liu, Chang-Jun

    Dimethyl ether (DME), with its non-toxic character, high H/C ratio and high-energy volumetric density, is an ideal resource for hydrogen production. In this work, hydrogen production from the decomposition of DME using corona discharge has been studied. The corona discharge plasma decomposition was conducted at ambient conditions. The effects of dilution gas (argon), flow rate, frequency and waveforms on the DME decomposition were investigated. The addition of dilution gas can significantly increase the hydrogen production rate. The highest hydrogen production rate with the lowest energy consumption presents at the flow rate of 27.5 Nml min -1. AC voltage is more favored than DC voltage for the production of hydrogen with less energy input. The optimal frequency is 2.0 kHz. The hydrogen production rate is also affected by the input waveform and decreases as following: sinusoid triangular > sinusoid > ramp > square, whereas the sinusoid waveform shows the highest energy efficiency. The corona discharge decomposition of DME is leading to a simple, easy and convenient hydrogen production with no needs of catalyst and external heating.

  2. Catalytic activity of mono and bimetallic Zn/Cu/MWCNTs catalysts for the thermocatalyzed conversion of methane to hydrogen

    Science.gov (United States)

    Erdelyi, B.; Oriňak, A.; Oriňaková, R.; Lorinčík, J.; Jerigová, M.; Velič, D.; Mičušík, M.; Omastová, M.; Smith, R. M.; Girman, V.

    2017-02-01

    Mono and bimetallic multiwalled carbon nanotubes (MWCNTs) fortified with Cu and Zn metal particles were studied to improve the efficiency of the thermocatalytic conversion of methane to hydrogen. The surface of the catalyst and the dispersion of the metal particles were studied by scanning electron microscopy (SEM), secondary ion mass spectrometry (SIMS) and with energy-dispersive X-ray spectroscopy (EDS). It was confirmed that the metal particles were successfully dispersed on the MWCNT surface and XPS analysis showed that the Zn was oxidised to ZnO at high temperatures. The conversion of methane to hydrogen during the catalytic pyrolysis was studied by pyrolysis gas chromatography using different amounts of catalyst. The best yields of hydrogen were obtained using pyrolysis conditions of 900 °C and 1.2 mg of Zn/Cu/MWCNT catalyst for 1.5 mL of methane.The initial conversion of methane to hydrogen obtained with Zn/Cu/MWCNTs was 49%, which represent a good conversion rate of methane to hydrogen for a non-noble metal catalyst.

  3. Catalytic Glycerol Hydrodeoxygenation under Inert Atmosphere: Ethanol as a Hydrogen Donor

    Directory of Open Access Journals (Sweden)

    Efterpi S. Vasiliadou

    2014-12-01

    Full Text Available Glycerol hydrodeoxygenation to 1,2-propanediol (1,2-PDO is a reaction of high interest. However, the need for hydrogen supply is a main drawback of the process. According to the concept investigated here, 1,2-propanediol is efficiently formed using bio-glycerol feedstock with H2 formed in situ via ethanol aqueous phase reforming. Ethanol is thought to be a promising H2 source, as it is alcohol that can be used instead of methanol for transesterification of oils and fats. The H2 generated is consumed in the tandem reaction of glycerol hydrodeoxygenation. The reaction cycle proceeds in liquid phase at 220–250 °C and 1.5–3.5 MPa initial N2 pressure for a 2 and 4-h reaction time. Pt-, Ni- and Cu-based catalysts have been synthesized, characterized and evaluated in the reaction. Among the materials tested, Pt/Fe2O3-Al2O3 exhibited the most promising performance in terms of 1,2-propanediol productivity, while reusability tests showed a stable behavior. Structural integrity and no formation of carbonaceous deposits were verified via Temperature Programmed Desorption of hydrogen (TPD-H2 and thermogravimetric analysis of the fresh and used Pt/FeAl catalyst. A study on the effect of various operating conditions (reaction time, temperature and pressure indicated that in order to maximize 1,2-propanediol productivity and yield, milder reaction conditions should be applied. The highest 1,2-propanediol yield, 53% (1.1 g1,2-PDO gcat−1·h−1, was achieved at a lower reaction temperature of 220 °C.

  4. Potential application of anaerobic extremophiles for hydrogen production

    Science.gov (United States)

    Pikuta, Elena V.; Hoover, Richard B.

    2004-11-01

    In processes of the substrate fermentation most anaerobes produce molecular hydrogen as a waste end product, which often controls the culture growth as an inhibitor. Usually in nature the hydrogen is easily removed from an ecosystem, due to its physical features, and an immediate consumption by the secondary anaerobes that sometimes behave as competitors for electron donors; a classical example of this kind of substrate competition in anaerobic microbial communities is the interaction between methanogens and sulfate- or sulfur-reducers. Previously, on the mixed cultures of anaerobes at neutral pH, it was demonstrated that bacterial hydrogen production could provide a good alternative energy source. At neutral pH the original cultures could easily contaminated by methanogens, and the most unpleasant side effect of these conditions is the development of pathogenic bacteria. In both cases the rate of hydrogen production was dramatically decreased since some part of the hydrogen was transformed to methane, and furthermore, the cultivation with pathogenic contaminants on an industrial scale would create an unsafe situation. In our laboratory the experiments with obligately alkaliphilic bacteria producing hydrogen as an end metabolic product were performed at different conditions. The mesophilic, haloalkaliphilic and obligately anaerobic bacterium Spirochaeta americana ASpG1T was studied and various cultivation regimes were compared for the most effective hydrogen production. In a highly mineralized media with pH 9.5-10.0 not many known methanogens are capable of growth, and the probability of developing pathogenic contaminants is theoretically is close to zero (in medicine carbonate- saturated solutions are applied as antiseptics). Therefore the cultivation of alkaliphilic hydrogen producing bacteria could be considered as a safe and economical process for large-scale industrial bio-hydrogen production in the future. Here we present and discuss the experimental data

  5. Production of bioplastics and hydrogen gas by photosynthetic microorganisms

    Science.gov (United States)

    Yasuo, Asada; Masato, Miyake; Jun, Miyake

    1998-03-01

    Our efforts have been aimed at the technological basis of photosynthetic-microbial production of materials and an energy carrier. We report here accumulation of poly-(3-hydroxybutyrate) (PHB), a raw material of biodegradable plastics and for production of hydrogen gas, and a renewable energy carrier by photosynthetic microorganisms (tentatively defined as cyanobacteria plus photosynthetic bateria, in this report). A thermophilic cyanobacterium, Synechococcus sp. MA19 that accumulates PHB at more than 20% of cell dry wt under nitrogen-starved conditions was isolated and microbiologically identified. The mechanism of PHB accumulation was studied. A mesophilic Synechococcus PCC7942 was transformed with the genes encoding PHB-synthesizing enzymes from Alcaligenes eutrophus. The transformant accumulated PHB under nitrogen-starved conditions. The optimal conditions for PHB accumulation by a photosynthetic bacterium grown on acetate were studied. Hydrogen production by photosynthetic microorganisms was studied. Cyanobacteria can produce hydrogen gas by nitrogenase or hydrogenase. Hydrogen production mediated by native hydrogenase in cyanobacteria was revealed to be in the dark anaerobic degradation of intracellular glycogen. A new system for light-dependent hydrogen production was targeted. In vitro and in vivo coupling of cyanobacterial ferredoxin with a heterologous hydrogenase was shown to produce hydrogen under light conditions. A trial for genetic trasformation of Synechococcus PCC7942 with the hydrogenase gene from Clostridium pasteurianum is going on. The strong hydrogen producers among photosynthetic bacteria were isolated and characterized. Co-culture of Rhodobacter and Clostriumdium was applied to produce hydrogen from glucose. Conversely in the case of cyanobacteria, genetic regulation of photosynthetic proteins was intended to improve conversion efficiency in hydrogen production by the photosynthetic bacterium, Rhodobacter sphaeroides RV. A mutant acquired by

  6. Hydrogen production from glucose by anaerobes.

    Science.gov (United States)

    Ogino, Hiroyasu; Miura, Takashi; Ishimi, Kosaku; Seki, Minoru; Yoshida, Hiroyuki

    2005-01-01

    Various anaerobes were cultivated in media containing glucose. When 100 mL of thioglycollate medium containing 2.0% (w/v) glucose was used, Clostridium butyricum ATCC 859, NBRC 3315, and NBRC 13949 evolved 227-243 mL of biogas containing about 180 mL of hydrogen in 1 day. Although some strains had some resistance against oxygen, C. butyricum ATCC 859 and 860 did not have it. C. butyricum NBRC 3315 and Enterobacter aerogenes NBRC 13534 produced hydrogen in the presence of glucose or pyruvic acid, and E. aerogenes NBRC 13534 produced hydrogen by not only glucose and pyruvic acid but also dextrin, sucrose, maltose, galactose, fructose, mannose, and mannitol. When a medium containing 0.5% (w/v) yeast extract and 2.0% (w/v) glucose was used, E. aerogenes NBRC 13534 evolved more biogas and hydrogen than C. butyricum NBRC 3315 in the absence of reducing agent.

  7. The catalytic reactions in the Cu-Li-Mg-H high capacity hydrogen storage system.

    Science.gov (United States)

    Braga, M H; El-Azab, A

    2014-11-14

    A family of hydrides, including the high capacity MgH2 and LiH, is reported. The disadvantages these hydrides normally display (high absorption/desorption temperatures and poor kinetics) are mitigated by Cu-hydride catalysis. This paper reports on the synthesis of novel CuLi0.08Mg1.42H4 and CuLi0.08Mg1.92H5 hydrides, which are structurally and thermodynamically characterized for the first time. The CuLi0.08Mg1.42H4 hydride structure in nanotubes is able to hold molecular H2, increasing the gravimetric and volumetric capacity of this compound. The catalytic effect these compounds show on hydride formation and decomposition of CuMg2 and Cu2Mg/MgH2, Li and LiH, Mg and MgH2 is analyzed. The Gibbs energy, decomposition temperature, and gravimetric capacity of the reactions occurring within the Cu-Li-Mg-H system are presented for the first time. First principles and phonon calculations are compared with experiments, including neutron spectroscopy. It is demonstrated that the most advantageous sample contains CuLi0.08Mg1.92 and (Li) ∼ Li2Mg3; it desorbs/absorbs hydrogen according to the reaction, 2CuLi0.08Mg1.42H4 + 2Li + 4MgH2 ↔ 2CuLi0.08Mg1.92 + Li2Mg3 + 8H2 at 114 °C (5.0 wt%) - 1 atm, falling within the proton exchange membrane fuel cell applications window. Finally the reaction 2CuLi0.08Mg1.42H4 + MgH2 ↔ 2CuLi0.08Mg1.92 + 5H2 at 15 °C (4.4 wt%) - 1 atm is found to be the main reaction of the samples containing CuLi0.08Mg1.92 that were analyzed in this study.

  8. 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.

  9. Electrolytic production and dispensing of hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, C.E.; Kuhn, I.F. Jr. [Directed Technologies, Inc., Arlington, VA (United States)

    1995-09-01

    The fuel cell electric vehicle (FCEV) is undoubtedly the only option that can meet both the California zero emission vehicle (ZEV) standard and the President`s goal of tripling automobile efficiency without sacrificing performance in a standard 5-passenger vehicle. The three major automobile companies are designing and developing FCEVs powered directly by hydrogen under cost-shared contracts with the Department of Energy. Once developed, these vehicles will need a reliable and inexpensive source of hydrogen. Steam reforming of natural gas would produce the least expensive hydrogen, but funding may not be sufficient initially to build both large steam reforming plants and the transportation infrastructure necessary to deliver that hydrogen to geographically scattered FCEV fleets or individual drivers. This analysis evaluates the economic feasibility of using small scale water electrolysis to provide widely dispersed but cost-effective hydrogen for early FCEV demonstrations. We estimate the cost of manufacturing a complete electrolysis system in large quantities, including compression and storage, and show that electrolytic hydrogen could be cost competitive with fully taxed gasoline, using existing residential off-peak electricity rates.

  10. Hydrogen production from biodiesel byproduct by immobilized Enterobacter aerogenes.

    Science.gov (United States)

    Han, Jinmi; Lee, Dohoon; Cho, Jinku; Lee, Jeewon; Kim, Sangyong

    2012-01-01

    The recent rapid growth of the biodiesel industry has generated a significant amount of glycerol as a byproduct. As a result, the price of glycerol is currently relatively low, making it an attractive starting material for the production of chemicals with higher values. Crude glycerol can be directly converted through microbial fermentation into various chemicals such as hydrogen. In this study, we optimized immobilization of a facultative hydrogen producing microorganism, Enterobacter aerogenes, with the goal of developing biocatalysts that was appropriate for the continuous hydrogen production from glycerol. Several carriers were tested and agar was found to be the most effective. In addition, it was clearly shown that variables such as the carrier content and cell loading should be controlled for the immobilization of biocatalysts with high hydrogen productivity, stability, and reusability. After optimization of these variables, we were able to obtain reusable biocatalysts that could directly convert the byproduct stream from biodiesel processes into hydrogen in continuous processes.

  11. Dialkylimidazolium ionic liquids as electrolytes for hydrogen production from water electrolysis

    Energy Technology Data Exchange (ETDEWEB)

    De Souza, Roberto F.; Padilha, Janine C.; Goncalves, Reinaldo S. [Department of Physical Chemistry, Institute of Chemistry, UFRGS, Av. Bento Goncalves, 9500, Porto Alegre, RS 91501-970 (Brazil); Rault-Berthelot, Joeelle [Laboratoire d ' Electrochimie Moleculaire et Macromoleculaire, UMR CNRS no. 6510 - Universite de Rennes 1, Institut de Chimie de Rennes, Campus Beaulieu, 35042 Rennes (France)

    2006-02-01

    Imidazolium ionic liquids (ILs) such as BMI.BF{sub 4} and BMI.PF{sub 6} were studied by cyclic voltammetry (CV). BMI.BF{sub 4} was used as an electrolyte for hydrogen production through water electrolysis. The system using this ionic liquid in a conventional electrochemical cell with platinum electrodes at room temperature and atmospheric pressure gives current densities (j) higher than 20mAcm{sup -2} and efficiencies of more than 94.5%. The catalytic activity of the electrode surface was not affected during the electrolyses mainly due to the chemical stability of the IL. (author)

  12. Study of hydrogen production from wind power in Algeria

    Energy Technology Data Exchange (ETDEWEB)

    Aiche-Hamane, Lilia; Belhamel, Maiouf; Benyoucef, Boumedienne; Hamane, Mustapha [Centre for Development of Renewable Energies (CDER), Alger (Algeria)

    2010-07-01

    An overview of the potentiality of hydrogen production from wind power in Algeria has been given in this study. Wind resource assessment has been presented in cartographic form and windy sites have been identified for wind power application. A system constituted by a wind turbine, an electrolyser and a power conditioning device have been proposed for the study of hydrogen production in the southwest region of Algeria. For this purpose, the transient system simulation program (TRNSYS) have been used. The results obtained showed the sensitivity of hydrogen production to the wind resource trend and the importance of optimisation of the electrolyser according to the power produced by the wind turbine. (orig.)

  13. Estimation of bacterial hydrogen sulfide production in vitro

    Directory of Open Access Journals (Sweden)

    Amina Basic

    2015-06-01

    Full Text Available Oral bacterial hydrogen sulfide (H2S production was estimated comparing two different colorimetric methods in microtiter plate format. High H2S production was seen for Fusobacterium spp., Treponema denticola, and Prevotella tannerae, associated with periodontal disease. The production differed between the methods indicating that H2S production may follow different pathways.

  14. Technical suitability mapping of feedstocks for biological hydrogen production

    NARCIS (Netherlands)

    Panagiotopoulos, I.A.; Karaoglanoglou, L.S.; Koullas, D.P.; Bakker, R.R.; Claassen, P.A.M.; Koukios, E.G.

    2015-01-01

    The objective of this work was to map and compare the technical suitability of different raw materials for biological hydrogen production. Our model was based on hydrogen yield potential, sugar mobilization efficiency, fermentability and coproduct yield and value. The suitability of the studied r

  15. On-Board Hydrogen Gas Production System For Stirling Engines

    Science.gov (United States)

    Johansson, Lennart N.

    2004-06-29

    A hydrogen production system for use in connection with Stirling engines. The production system generates hydrogen working gas and periodically supplies it to the Stirling engine as its working fluid in instances where loss of such working fluid occurs through usage through operation of the associated Stirling engine. The hydrogen gas may be generated by various techniques including electrolysis and stored by various means including the use of a metal hydride absorbing material. By controlling the temperature of the absorbing material, the stored hydrogen gas may be provided to the Stirling engine as needed. A hydrogen production system for use in connection with Stirling engines. The production system generates hydrogen working gas and periodically supplies it to the Stirling engine as its working fluid in instances where loss of such working fluid occurs through usage through operation of the associated Stirling engine. The hydrogen gas may be generated by various techniques including electrolysis and stored by various means including the use of a metal hydride absorbing material. By controlling the temperature of the absorbing material, the stored hydrogen gas may be provided to the Stirling engine as needed.

  16. Improvements in Fermentative Biological Hydrogen Production Through Metabolic Engineering

    Energy Technology Data Exchange (ETDEWEB)

    Hallenbeck, P. C.; Ghosh, D.; Sabourin-Provost, G.

    2009-07-01

    Dramatically rising oil prices and increasing awareness of the dire environmental consequences of fossil fuel use, including startling effects of climate change, are refocusing attention world-wide on the search for alternative fuels. Hydrogen is poised to become an important future energy carrier. Renewable hydrogen production is pivotal in making it a truly sustainable replacement for fossil fuels. (Author)

  17. Simulation of a hydrogen production and purification system for a PEM fuel-cell using bioethanol as raw material

    Energy Technology Data Exchange (ETDEWEB)

    Giunta, Pablo; Amadeo, Norma; Laborde, Miguel [Facultad de Ingenieria, Universidad de Buenos Aires, Laboratorio de Procesos Cataliticos, Pabellon de Industrias, Ciudad Universitaria, 1428 Buenos Aires (Argentina); Mosquera, Carlos [Facultad de Ingenieria, Universidad de Buenos Aires, Departamento de Fisica, 1063 Buenos Aires (Argentina)

    2007-01-10

    A process to produce 'fuel-cell grade' hydrogen from ethanol steam reforming is analyzed from a thermodynamic point of view. The hydrogen purification process consists of WGS and COPROX reactors. Equations to evaluate the efficiency of the system, including the fuel cell, are presented. A heat exchange network is proposed in order to improve the exploitation of the available power. The effect of key variables such as the reformer temperature and the ethanol/water molar feed ratio on the fuel-cell efficiency is discussed. Results show that it is feasible to carry out the energy integration of the hydrogen catalytic production and purification-PEM fuel-cell system, using ethanol as raw material. The technology of 'fuel-cell grade' hydrogen production using ethanol as raw material is a very attractive alternative to those technologies based in fossil fuels. (author)

  18. Catalytic Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts

    Directory of Open Access Journals (Sweden)

    Rodiansono Rodiansono

    2015-07-01

    Full Text Available A bulk structure of inexpensive intermetallic nickel-tin (Ni-Sn alloys catalysts demonstrated highly selective in the hydrogenation of levulinic acid in water into g-valerolactone. The intermetallic Ni-Sn catalysts were synthesized via a very simple thermochemical method from non-organometallic precursor at low temperature followed by hydrogen treatment at 673 K for 90 min. The molar ratio of nickel salt and tin salt was varied to obtain the corresponding Ni/Sn ratio of 4.0, 3.0, 2.0, 1.5, and 0.75. The formation of Ni-Sn alloy species was mainly depended on the composition and temperature of H2 treatment. Intermetallics Ni-Sn that contain Ni3Sn, Ni3Sn2, and Ni3Sn4 alloy phases are known to be effective heterogeneous catalysts for levulinic acid hydrogenation giving very excellence g-valerolactone yield of >99% at 433 K, initial H2 pressure of 4.0 MPa within 6 h. The effective hydrogenation was obtained in H2O without the formation of by-product. Intermetallic Ni-Sn(1.5 that contains Ni3Sn2 alloy species demonstrated very stable and reusable catalyst without any significant loss of its selectivity. © 2015 BCREC UNDIP. All rights reserved. Received: 26th February 2015; Revised: 16th April 2015; Accepted: 22nd April 2015  How to Cite: Rodiansono, R., Astuti, M.D., Ghofur, A., Sembiring, K.C. (2015. Catalytic Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts. Bulletin of Chemical Reaction Engineering & Catalysis, 10 (2: 192-200. (doi:10.9767/bcrec.10.2.8284.192-200Permalink/DOI: http://dx.doi.org/10.9767/bcrec.10.2.8284.192-200  

  19. Role of the chemically non-innocent ligand in the catalytic formation of hydrogen and carbon dioxide from methanol and water with the metal as the spectator.

    Science.gov (United States)

    Li, Haixia; Hall, Michael B

    2015-09-30

    The catalytic mechanism for the production of H2 and CO2 from CH3OH and H2O by [K(dme)2][Ru(H) (trop2dad)] (K(dme)2.1_exp) was investigated by density functional theory (DFT) calculations. Since the reaction occurs under mild conditions and at reasonable rates, it could be considered an ideal way to use methanol to store hydrogen. The predicted mechanism begins with the dehydrogenation of methanol to formaldehyde through a new ligand-ligand bifunctional mechanism, where two hydrogen atoms of CH3OH eliminate to the ligand's N and C atoms, a mechanism that is more favorable than the previously known mechanisms, β-H elimination, or the metal-ligand bifunctional. The key initiator of this first step is formed by migration of the hydride in 1 from the ruthenium to the meta-carbon atom, which generates 1″ with a frustrated Lewis pair in the ring between N and C. Hydroxide, formed when 1″ cleaves H2O, reacts rapidly with CH2O to give H2C(OH)O(-), which subsequently donates a hydride to 6 to generate HCOOH and 5. HCOOH then protonates 5 to give formate and a neutral complex, 4, with a fully hydrogenated ligand. The hydride of formate transfers to 6, releasing CO2. The fully hydrogenated complex, 4, is first deprotonated by OH(-) to form 5, which then releases hydrogen to regenerate the catalyst, 1″. In this mechanism, which explains the experimental observations, the whole reaction occurs on the chemically non-innocent ligand with the ruthenium atom appearing as a spectator.

  20. Aqueous-phase catalytic hydrogenation of furfural to cyclopentanol over Cu-Mg-Al hydrotalcites derived catalysts:Model reaction for upgrading of bio-oil

    Institute of Scientific and Technical Information of China (English)

    Minghao; Zhou; Zuo; Zeng; Hongyan; Zhu; Guomin; Xiao; Rui; Xiao

    2014-01-01

    A series of Cu-Mg-Al hydrotalcites derived oxides with a(Cu+Mg)/Al mole ratio of 3 and varied Cu/Mg mole ratio(from 0.07 to 0.30) were prepared by co-precipitation and calcination methods, then they were introduced to the hydrogenation of furfural in aqueous-phase. Effects of Cu/Mg mole ratio, reaction temperature, initial hydrogen pressure, reaction time and catalyst amount on the conversion rate of furfural as well as the selectivity toward desired product cyclopentanol were systematically investigated. The conversion of furfural over calcined hydrotalcite catalyst with a Cu/Mg mole ratio of 0.2 was up to 98.5% when the reaction was carried out under 140 ?C and the initial hydrogen pressure of 4 MPa for 10 h, while the selectivity toward cyclopentanol was up to 94.8%. The catalysts were characterized by XRD and SEM. XRD diffraction of all the samples showed characteristic pattern of hydrotalcite with varied peak intensity as a result of different Cu content. The catalytic activity was improved gradually with the increase of Cu component in the hydrotalcite.

  1. Production of hydrogen from CH{sub 4}, CO or H{sub 2}S in gliding electric discharges

    Energy Technology Data Exchange (ETDEWEB)

    Czernichowski, A. [GlidArc Technologies Sarl, Orleans (France)

    2000-05-01

    A newly developed method to extract hydrogen from natural gas or biogas through pyrolysis or reforming into synthesis gas was presented. The new method, which is more energy efficient and environmentally friendly compared to classical hydrogen production technologies, uses a powerful and extremely active non-thermal plasma source called GlidArc. GlidArc refers to multiple gliding electric discharges. The method is ideally suited for hydrogen production from light hydrocarbons, any methane or carbon dioxide mixtures, gases containing carbon monoxide or waste acid gases containing hydrogen sulphide. These non-equilibrium discharges act as an enthalpy and or catalytic activation source. This paper presented examples of the following: (1) pyrolysis of natural gas, (2) hydrogen from synthesis gas, (3) GlidArc assisted steam reforming of methane, (4) GlidArc assisted partial oxidation of methane, (5) hydrogen production via water shift of carbon monoxide and (6) hydrogen extraction from hydrogen sulphide. The energy balances in each situation demonstrate that up to 40 per cent of input electric energy goes directly into endothermic processes without the use of a catalyst. GlidArc can be easily integrated into nearly any process and is very compact for easy installation in restricted areas. The GlidArc 1 reactor is patented by both U.S. and French patents. Patent is pending on the new GlidArc-II reactor which is better adapted for natural gas and other gas processing. 14 refs., 1 tab., 2 figs.

  2. Selective Catalytic Oxidation of Hydrogen Sulfide to Elemental Sulfur from Coal-Derived Fuel Gases

    Energy Technology Data Exchange (ETDEWEB)

    Gardner, Todd H.; Berry, David A.; Lyons, K. David; Beer, Stephen K.; Monahan, Michael J.

    2001-11-06

    The development of low cost, highly efficient, desulfurization technology with integrated sulfur recovery remains a principle barrier issue for Vision 21 integrated gasification combined cycle (IGCC) power generation plants. In this plan, the U. S. Department of Energy will construct ultra-clean, modular, co-production IGCC power plants each with chemical products tailored to meet the demands of specific regional markets. The catalysts employed in these co-production modules, for example water-gas-shift and Fischer-Tropsch catalysts, are readily poisoned by hydrogen sulfide (H{sub 2}S), a sulfur contaminant, present in the coal-derived fuel gases. To prevent poisoning of these catalysts, the removal of H{sub 2}S down to the parts-per-billion level is necessary. Historically, research into the purification of coal-derived fuel gases has focused on dry technologies that offer the prospect of higher combined cycle efficiencies as well as improved thermal integration with co-production modules. Primarily, these concepts rely on a highly selective process separation step to remove low concentrations of H{sub 2}S present in the fuel gases and produce a concentrated stream of sulfur bearing effluent. This effluent must then undergo further processing to be converted to its final form, usually elemental sulfur. Ultimately, desulfurization of coal-derived fuel gases may cost as much as 15% of the total fixed capital investment (Chen et al., 1992). It is, therefore, desirable to develop new technology that can accomplish H{sub 2}S separation and direct conversion to elemental sulfur more efficiently and with a lower initial fixed capital investment.

  3. Hydrogen production econometric studies. [hydrogen and fossil fuels

    Science.gov (United States)

    Howell, J. R.; Bannerot, R. B.

    1975-01-01

    The current assessments of fossil fuel resources in the United States were examined, and predictions of the maximum and minimum lifetimes of recoverable resources according to these assessments are presented. In addition, current rates of production in quads/year for the fossil fuels were determined from the literature. Where possible, costs of energy, location of reserves, and remaining time before these reserves are exhausted are given. Limitations that appear to hinder complete development of each energy source are outlined.

  4. Rational Design of Porous Conjugated Polymers and Roles of Residual Palladium for Photocatalytic Hydrogen Production.

    Science.gov (United States)

    Li, Lianwei; Cai, Zhengxu; Wu, Qinghe; Lo, Wai-Yip; Zhang, Na; Chen, Lin X; Yu, Luping

    2016-06-22

    Developing highly efficient photocatalyts for water splitting is one of the grand challenges in solar energy conversion. Here, we report the rational design and synthesis of porous conjugated polymer (PCP) that photocatalytically generates hydrogen from water splitting. The design mimics natural photosynthetics systems with conjugated polymer component to harvest photons and the transition metal part to facilitate catalytic activities. A series of PCPs have been synthesized with different light harvesting chromophores and transition metal binding bipyridyl (bpy) sites. The photocatalytic activity of these bpy-containing PCPs can be greatly enhanced due to the improved light absorption, better wettability, local ordering structure, and the improved charge separation process. The PCP made of strong and fully conjugated donor chromophore DBD (M4) shows the highest hydrogen production rate at ∼33 μmol/h. The results indicate that copolymerization between a strong electron donor and weak electron acceptor into the same polymer chain is a useful strategy for developing efficient photocatalysts. This study also reveals that the residual palladium in the PCP networks plays a key role for the catalytic performance. The hydrogen generation activity of PCP photocatalyst can be further enhanced to 164 μmol/h with an apparent quantum yield of 1.8% at 350 nm by loading 2 wt % of extra platinum cocatalyst.

  5. Renewable hydrogen production for fossil fuel processing

    Energy Technology Data Exchange (ETDEWEB)

    Greenbaum, E.; Lee, J.W.; Tevault, C.V. [and others

    1995-06-01

    In the fundamental biological process of photosynthesis, atmospheric carbon dioxide is reduced to carbohydrate using water as the source of electrons with simultaneous evolution of molecular oxygen: H{sub 2}O + CO{sub 2} + light {yields} O{sub 2} + (CH{sub 2}O). It is well established that two light reactions, Photosystems I and II (PSI and PSII) working in series, are required to perform oxygenic photosynthesis. Experimental data supporting the two-light reaction model are based on the quantum requirement for complete photosynthesis, spectroscopy, and direct biochemical analysis. Some algae also have the capability to evolve molecular hydrogen in a reaction energized by the light reactions of photosynthesis. This process, now known as biophotolysis, can use water as the electron donor and lead to simultaneous evolution of molecular hydrogen and oxygen. In green algae, hydrogen evolution requires prior incubation under anaerobic conditions. Atmospheric oxygen inhibits hydrogen evolution and also represses the synthesis of hydrogenase enzyme. CO{sub 2} fixation competes with proton reduction for electrons relased from the photosystems. Interest in biophotolysis arises from both the questions that it raises concerning photosynthesis and its potential practical application as a process for converting solar energy to a non-carbon-based fuel. Prior data supported the requirement for both Photosystem I and Photosystem II in spanning the energy gap necessary for biophotolysis of water to oxygen and hydrogen. In this paper we report the at PSII alone is capable of driving sustained simultaneous photoevolution of molecular hydrogen and oxygen in an anaerobically adapted PSI-deficient strain of Chlamydomonas reinhardtii, mutant B4, and that CO{sub 2} competes as an electron acceptor.

  6. Glycerol and bioglycerol conversion in supercritical water for hydrogen production.

    Science.gov (United States)

    Yu-Wu, Q M; Weiss-Hortala, E; Barna, R; Boucard, H; Bulza, S

    2012-01-01

    Catalytic transesterification of vegetable oils leads to biodiesel and an alkaline feed (bioglycerol and organic residues, such as esters, alcohols. . .). The conversion ofbioglycerol into valuable organic molecules represents a sustainable industrial process leading to the valorization of a renewable organic resource. The physicochemical properties in the supercritical domain (T > 374 degrees C, P > 22.1 MPa) transform water into a solvent for organics and a reactant favouring radical reactions. In this context, the conversion ofbioglycerol in supercritical water (SCW) into platform molecules and/or high energetic gases (hydrogen, hydrocarbons) could represent an interesting valorization process. The reported research results concern the conversion of bioglycerol compared to pure glycerol. The experiments have been done in batch autoclaves (5 ml and 500 ml stirred). Solutions of pure (5 or 10 wt%) and crude (3.5 wt%) glycerol have been processed with or without catalyst (K2CO3 1.5 wt%) in the range of 450-600 degrees C. The molecular formula of bioglycerol was determined as C4.3H9.7O1.8Na0.1Si0.08. Glycerol was partially decomposed in the batch systems during the heating (42% before reaching 420 degrees C) and some intermediates (propanediol, ethylene glycol . . .) were quantified, leading to a proposition of a reaction pathway. Acrolein, a valuable platform molecule, was mainly produced in the absence of catalyst. No solid phase was recovered after SCW conversion of pure and bioglycerol in batch reactors. The optimal parameters for gasification were 600 degrees C, 25 MPa for bioglycerol and 525 degrees C, 25 MPa, for pure glycerol. In these operating conditions, 1 kg of pure or bioglycerol leads to 15 and, respectively, 10 mol of hydrogen. Supercritical water gasification of crude glycerol favoured the generation of light hydrocarbons, while pure glycerol promoted H2 production. SCW conversion of glycerol (pure and crude) allows to obtain simultaneously energetic

  7. Biological hydrogen production by moderately thermophilic anaerobic bacteria

    Energy Technology Data Exchange (ETDEWEB)

    HP Goorissen; AJM Stams [Laboratory of Microbiology, Wageningen University and Research centre Wageningen (Netherlands)

    2006-07-01

    This study focuses on the biological production of hydrogen at moderate temperatures (65-75 C) by anaerobic bacteria. A survey was made to select the best (moderate) thermophiles for hydrogen production from cellulolytic biomass. From this survey we selected Caldicellulosiruptor saccharolyticus (a gram-positive bacterium) and Thermotoga elfii (a gram-negative bacterium) as potential candidates for biological hydrogen production on mixtures of C{sub 5}-C{sub 6} sugars. Xylose and glucose were used as model substrates to describe growth and hydrogen production from hydrolyzed biomass. Mixed substrate utilization in batch cultures revealed differences in the sequence of substrate consumption and in catabolites repression of the two microorganisms. The regulatory mechanisms of catabolites repression in these microorganisms are not known yet. (authors)

  8. IEA Energy Technology Essentials: Hydrogen Production and Distribution

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2007-04-15

    The IEA Energy Technology Essentials series offers concise four-page updates on the different technologies for producing, transporting and using energy. Hydrogen Production and Distribution are the topics covered in this edition.

  9. Hydrogen Production by Homogeneous Catalysis: Alcohol Acceptorless Dehydrogenation

    DEFF Research Database (Denmark)

    Nielsen, Martin

    2015-01-01

    in hydrogen production from biomass using homogeneous catalysis. Homogeneous catalysis has the advance of generally performing transformations at much milder conditions than traditional heterogeneous catalysis, and hence it constitutes a promising tool for future applications for a sustainable energy sector...

  10. Hydrogen production by Clostridium thermolacticum during continuous fermentation of lactose

    Energy Technology Data Exchange (ETDEWEB)

    Collet, C.; Adler, N.; Schwitzguebel, J.P.; Peringer, P. [Swiss Federal Inst. of Technology Lausanne (EPFL) (Switzerland). Lab. for Environmental Biotechnology

    2004-11-01

    In the production of acetate by Clostridium thermolacticum growing on lactose, considerable amounts of hydrogen were generated. Lactose available in large amounts from milk permeate, a waste stream of the dairy industry, appears to be a valuable substrate for cheap production of biohydrogen. In this study, continuous cultivation of C. thermolacticum was carried out in a bioreactor, under anaerobic thermophilic conditions, on minimal medium containing 10 g l{sup -1} lactose. Different dilution rates and pH were tested. C. thermolacticum growing on lactose produced acetate, ethanol and lactate in the liquid phase. For all conditions tested, hydrogen was the main product in the gas phase. Hydrogen specific production higher than 5 mmol H{sub 2} (g cell){sup -1} h{sup -1} was obtained. By operating this fermentation at high-dilution rate and alkaline pH, the hydrogen content in the gas phase was maximized. (author)

  11. Biophotolysis, hydrogen, production and algal culture technology

    Energy Technology Data Exchange (ETDEWEB)

    Skulberg, O.M. [Norwegian Inst. for Water Research, Oslo (Norway)

    1995-12-31

    In this essay the importance and place of biophotolysis in the hydrogen energy system is described. The biophotolysis of water is achieved by two biochemical processes carried out by the activity of chlorophyll containing reaction centres coupled to hydrogenase and nitrogenase. Micro algae belonging to the classes Chlorophyceae and Cyanophyceae can produce molecular hydrogen by the decomposition of water using solar energy. Among Anoxyphotobactelia organisms of the families Chrorna iaceae and Chlorobiaceae are also used for the bioengineering development of biophotolysis. A review is presented of the organisms and the processes involved in the context of their applications for algal culture technology. 2 tabs., 52 refs.

  12. Exergetic life cycle assessment of hydrogen production from renewables

    Science.gov (United States)

    Granovskii, Mikhail; Dincer, Ibrahim; Rosen, Marc A.

    Life cycle assessment is extended to exergetic life cycle assessment and used to evaluate the exergy efficiency, economic effectiveness and environmental impact of producing hydrogen using wind and solar energy in place of fossil fuels. The product hydrogen is considered a fuel for fuel cell vehicles and a substitute for gasoline. Fossil fuel technologies for producing hydrogen from natural gas and gasoline from crude oil are contrasted with options using renewable energy. Exergy efficiencies and greenhouse gas and air pollution emissions are evaluated for all process steps, including crude oil and natural gas pipeline transportation, crude oil distillation and natural gas reforming, wind and solar electricity generation, hydrogen production through water electrolysis, and gasoline and hydrogen distribution and utilization. The use of wind power to produce hydrogen via electrolysis, and its application in a fuel cell vehicle, exhibits the lowest fossil and mineral resource consumption rate. However, the economic attractiveness, as measured by a "capital investment effectiveness factor," of renewable technologies depends significantly on the ratio of costs for hydrogen and natural gas. At the present cost ratio of about 2 (per unit of lower heating value or exergy), capital investments are about five times lower to produce hydrogen via natural gas rather than wind energy. As a consequence, the cost of wind- and solar-based electricity and hydrogen is substantially higher than that of natural gas. The implementation of a hydrogen fuel cell instead of an internal combustion engine permits, theoretically, an increase in a vehicle's engine efficiency of about of two times. Depending on the ratio in engine efficiencies, the substitution of gasoline with "renewable" hydrogen leads to (a) greenhouse gas (GHG) emissions reductions of 12-23 times for hydrogen from wind and 5-8 times for hydrogen from solar energy, and (b) air pollution (AP) emissions reductions of 38

  13. Summary of research on hydrogen production from fossil fuels conducted at NETL

    Energy Technology Data Exchange (ETDEWEB)

    Shamsi, Abolghasem

    2008-03-30

    In this presentation we will summarize the work performed at NETL on the production of hydrogen via partial oxidation/dry reforming of methane and catalytic decomposition of hydrogen sulfide. We have determined that high pressure resulted in greater carbon formation on the reforming catalysts, lower methane and CO2 conversions, as well as a H2/CO ratio. The results also showed that Rh/alumina catalyst is the most resistant toward carbon deposition both at lower and at higher pressures. We studied the catalytic partial oxidation of methane over Ni-MgO solid solutions supported on metal foams and the results showed that the foam-supported catalysts reach near-equilibrium conversions of methane and H2/CO selectivities. The rates of carbon deposition differ greatly among the catalysts, varying from 0.24 mg C/g cat h for the dipped foams to 7.0 mg C/g cat h for the powder-coated foams, suggesting that the exposed Cr on all of the foam samples may interact with the Ni-MgO catalyst to kinetically limit carbon formation. Effects of sulfur poisoning on reforming catalysts were studies and pulse sulfidation of catalyst appeared to be reversible for some of the catalysts but not for all. Under pulse sulfidation conditions, the 0.5%Rh/alumina and NiMg2Ox-1100ºC (solid solution) catalysts were fully regenerated after reduction with hydrogen. Rh catalyst showed the best overall activity, less carbon deposition, both fresh and when it was exposed to pulses of H2S. Sulfidation under steady state conditions significantly reduced catalyst activity. Decomposition of hydrogen sulfide into hydrogen and sulfur was studied over several supported metal oxides and metal oxide catalysts at a temperature range of 650-850°C. H2S conversions and effective activation energies were estimated using Arrhenius plots. The results of these studies will further our understanding of catalytic reactions and may help in developing better and robust catalysts for the production of hydrogen from fossil

  14. NGNP Process Heat Applications: Hydrogen Production Accomplishments for FY2010

    Energy Technology Data Exchange (ETDEWEB)

    Charles V Park

    2011-01-01

    This report summarizes FY10 accomplishments of the Next Generation Nuclear Plant (NGNP) Engineering Process Heat Applications group in support of hydrogen production technology development. This organization is responsible for systems needed to transfer high temperature heat from a high temperature gas-cooled reactor (HTGR) reactor (being developed by the INL NGNP Project) to electric power generation and to potential industrial applications including the production of hydrogen.

  15. In vitro hydrogen production by glucose dehydrogenase and hydrogenase

    Energy Technology Data Exchange (ETDEWEB)

    Woodward, J. [Oak Ridge National Lab., TN (United States)

    1996-10-01

    A new in vitro enzymatic pathway for the generation of molecular hydrogen from glucose has been demonstrated. The reaction is based upon the oxidation of glucose by Thermoplasma acidophilum glucose dehydrogenase with the concomitant oxidation of NADPH by Pyrococcus furiosus hydrogenase. Stoichiometric yields of hydrogen were produced from glucose with continuous cofactor recycle. This simple system may provide a method for the biological production of hydrogen from renewable sources. In addition, the other product of this reaction, gluconic acid, is a high-value commodity chemical.

  16. Photocatalytic Hydrogen Production by Direct Sunlight: A Laboratory Experiment

    Science.gov (United States)

    Koca, Atif; Sahin, Musa

    2003-11-01

    The demand for hydrogen will increase within the next decades as a result of the necessity to produce clean and environmentally and economically accepted fuels from natural and renewable energy resources. In principle, hydrogen has the potential to play an important role in future energy systems because of the diversity of its applications, the variety of ways in which it can be stored, its general environmental advantages, and especially because of the possibility of producing hydrogen by splitting water using photocatalysts and solar energy. Methods and techniques of photocatalytic reactions are covered in some detail in many undergraduate chemistry programs. However, many times in instructional settings, little attention is given to how it is used for the production of hydrogen. In the present investigation a photocatalytic hydrogen production experiment suitable for use in undergraduate chemistry laboratories is described. The experiment can be used to introduce students to the concept of a renewable and sustainable hydrogen energy system of the future, as well as its production techniques, and to demonstrate the use of a CdS/ZnS photocatalyst system for photocatalytic hydrogen production from direct sunlight.

  17. Hydrogenation of carbon dioxide for methanol production

    NARCIS (Netherlands)

    Ham, van der A.G.J.; Berg, van den H.; Benneker, A.; Simmelink, G.; Timmer, J.; Weerden, van S.

    2012-01-01

    A process for the hydrogenation of CO2 to methanol with a capacity of 10 kt/y methanol is designed in a systematic way. The challenge will be to obtain a process with a high net CO2 conversion. From initially four conceptual designs the most feasible is selected and designed in more detail. The feed

  18. Enrichment and hydrogen production by marine anaerobic hydrogen-producing microflora

    Institute of Scientific and Technical Information of China (English)

    CAI JinLing; WANG GuangCe; LI YanChuan; ZHU DaLing; PAN GuangHua

    2009-01-01

    Acid,alkali,heat-shock,KNO3 and control pretreatment methods applied to anaerobic sludge were evaluated for their ability to selectively enrich the marine hydrogen-producing mixed microflora.Seawater culture medium was used as the substrate.The hydrogen yield of pretreated microflora was higher than that of the un-pretreated control (P<0.05).Among the pretreatment methods studied,heat-shock pretreatment yielded the greatest hydrogen production,which was 14.6 times that of the control.When the effect of initial pH on hydrogen production of heat-shock pretreated samples was studied,hydrogen was produced over the entire pH range (pH 4-10).The hydrogen yield peaked at initial pH 8 (79 mL/g sucrose) and then steadily decreased as the initial pH increased.Sucrose consumption was high at neutral initial pH.During the process of hydrogen production,pH decreased gradually,which indicated that the acquired microflora consisted of acidogenic bacteria.

  19. Clean Hydrogen Production. Carbon Dioxide Free Alternatives. Project Phisico2

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Fierro, J. L.; Gonzalez, C.; Serrano, D.; Penelas, G.; Romero, M.; Marcos, M. J.; Rodriguez, C.

    2006-07-01

    The main goal of the PHISICO2 project, funded and promoted by Comunidad de Madrid, is the evaluation and optimisation of three different processes for the clean hydrogen production without carbon dioxide emission. Solar energy and associated Technologies are proposed to be jointly employed with the aim of improving the process efficiency and reducing the production costs. As a transition to the non-fossil fuel hydrogen economy, the thermocatalytic CO2-free production of hydrogen from natural gas will be considered. One of the most promising alternatives of this process is to develop a cheap and stable carbon-based catalyst able to efficiently decompose methane into a CO2-free hydrogen stream and solid carbon. Thus, not only pure hydrogen can be obtained through but also carbon with specific properties and commercial value can be produced. Another option to be explored is the splitting of water by means of solar light by means of two different approaches: (i) photodissociation promoted by semiconductor catalysts and (ii) thermochemical cycles in which a specific mixed oxide is first thermally reduced by sunlight and then reoxidized by steam in a second step with the parallel production of hydrogen. Indeed, option (i) implies necessarily the development of semiconductors with appropriate band-gap able to decompose water into hydrogen and oxygen in an efficient manner. Another critical issue will be the development of a strategy/concept that allows efficient separation of hydrogen and oxygen within the cell. In option (ii), the development of stable ferrites which act as the redox element of the cycle is also an important challenge. Finally, a 5 kW prototype solar engine water splitting, based on the mentioned thermochemical cycle, will developed and tested using concentrated solar light as an energy source. Moreover, thermodynamic and kinetic studies, reactor design, process optimisation, economical studies and comparison with conventional hydrogen production systems

  20. Hydrogenation of Isophthalonitrile with 1-Methylimidazole as an Effective Solvent for m-Xylenediamine Production

    Energy Technology Data Exchange (ETDEWEB)

    Chae, Tae Young; Row, Sung Wook; Yoo, Kye Sang; Lee, Sang Duek [Environment and Process Technology Division, Seoul (Korea, Republic of); Lee, Do Weon [University of Seoul, Seoul (Korea, Republic of)

    2006-03-15

    1-methylimidazole was shown to outperform the other organic solvents in this reaction. Moreover, amount of ammonia with using 1-methylimidazole as a solvent was lower than other processes. Thus, 1-methylimidazole is an attractive solvent in IPN hydrogenation for the production of MXDA. The correct choice of a solvent is a critical factor to govern the catalytic activity with desirable hydrogenation. Conventionally, organic materials such as aromatic hydrocarbons, aliphatic alcohols, aliphatic hydrocarbons, dimethylformamide and dioxane were employed in this reaction. Several MXDA producing processes with the organic solvent including m-xylene, pseudocumene, mesitylene, ethylbenzene, methylpyridine, benzonitrile, m-tolunitrile, MXDA and cyanopyridine were disclosed. However, the solvents and ammonia were vaporized under the operation conditions leading to amine cleavage with the resulting formation of methylbenzyl amines or the consumption of ammonia was still significant. Recently, some researchers reported that a high yield of MXDA was achieved using isopropanol under relatively low pressure condition; however, the consumption of ammonia was very significant.

  1. A novel rotary reactor configuration for simultaneous production of hydrogen and carbon nanofibers

    Energy Technology Data Exchange (ETDEWEB)

    Pinilla, J.L.; Utrilla, R.; Lazaro, M.J.; Suelves, I.; Moliner, R. [Instituto de Carboquimica CSIC, Miguel Luesma 4, 50018 Zaragoza (Spain); Palacios, J.M. [Instituto de Catalisis y Petroleoquimica CSIC, Cantoblanco, Marie Curie 2, 28049-Madrid (Spain)

    2009-10-15

    A novel reactor configuration, a rotary bed reactor (RBR), was used to study at large scale production the Catalytic Decomposition of Methane (CDM) into hydrogen and carbon nanofibers using a nickel-copper catalyst. The results were compared to those obtained in a fluidized bed reactor (FBR) under the same operating conditions. Tests carried out in the RBR provided higher hydrogen yields and more sustainable catalyst performance in comparison to the FBR. Additionally, the effect of the rotation speed and reaction temperature on the performance in the RBR of the nickel-copper catalyst was studied. The textural and structural properties of the carbon nanofibers produced were also studied by means of N{sub 2} adsorption, SEM and XRD, and compared to those obtained in the FBR set-up under the same operating conditions. (author)

  2. Effect of Pt promotion on Ni/Al2O3 for the selective catalytic reduction of NO with hydrogen

    Science.gov (United States)

    Mihet, Maria; Lazar, Mihaela D.; Borodi, G.; Almasan, V.

    2013-11-01

    Ni/Al2O3 (10 wt.% Ni) and Ni-Pt/Al2O3 (10 wt.% Ni, 0.5 wt.% Pt) were comparatively tested in the hydrogen selective catalytic reduction process (H2-SCR), at reaction temperatures below 350°C. Catalytic activity tests consisted in temperature programmed reactions (TPRea) under plug flow conditions from 50 to 350°C, with a temperature rate of 5°C/min, using a feed stream with a reactant ratio NO:H2 = 1:1.3 and a GHSV of 4500 h-1. Promotion with Pt increases the catalytic performances of the Ni based catalyst, in respect to NO conversion, N2 selectivity and N2 yield. The reaction temperatures for NO conversion above 95% decrease significantly due to Pt addition, from 250°C for Ni/Al2O3 to 125°C for Ni-Pt/Al2O3. Characterization of catalysts was performed by: X ray powder diffraction (XRD) for the estimation of Ni crystallite size, temperature programmed reduction (TPR) for the catalyst reducibility, temperature programmed desorption of hydrogen (H2-TPD) for the investigation of active sites and metal dispersion on the support, N2 adsorption-desorption isotherms at -196°C for the determination of total specific surface area and pore size distribution, and H/D isotopic exchange on the catalyst surface. At the request of the Proceedings Editor, and all authors of the paper, an updated version of this article was published on 14 January 2014. Data presented in Table 1 of the original paper contained errors which have been corrected in the updated and re-published article. The Corrigendum attached to the corrected article PDF file explains the errors in more detail.

  3. Biological hydrogen production measured in batch anaerobic respirometers.

    Science.gov (United States)

    Logan, Bruce E; Oh, Sang-Eun; Kim, In S; Van Ginkel, Steven

    2002-06-01

    The biological production of hydrogen from the fermentation of different substrates was examined in batch tests using heat-shocked mixed cultures with two techniques: an intermittent pressure release method (Owen method) and a continuous gas release method using a bubble measurement device (respirometric method). Under otherwise identical conditions, the respirometric method resulted in the production of 43% more hydrogen gas from glucose than the Owen method. The lower conversion of glucose to hydrogen using the Owen protocol may have been produced by repression of hydrogenase activity from high partial pressures in the gastight bottles, but this could not be proven using a thermodynamic/rate inhibition analysis. In the respirometric method, total pressure in the headspace never exceeded ambient pressure, and hydrogen typically composed as much as 62% of the headspace gas. High conversion efficiencies were consistently obtained with heat-shocked soils taken at different times and those stored for up to a month. Hydrogen gas composition was consistently in the range of 60-64% for glucose-grown cultures during logarithmic growth but declined in stationary cultures. Overall, hydrogen conversion efficiencies for glucose cultures were 23% based on the assumption of a maximum of 4 mol of hydrogen/ mol of glucose. Hydrogen conversion efficiencies were similar for sucrose (23%) and somewhat lower for molasses (15%) but were much lower for lactate (0.50%) and cellulose (0.075%).

  4. Bio-hydrogen Production Potential from Market Waste

    Directory of Open Access Journals (Sweden)

    Lanna Jaitalee

    2010-07-01

    Full Text Available This research studied bio-hydrogen production from vegetable waste from a fresh market in order to recover energy. A series of batch experiments were conducted to investigate the effects of initial volatile solids concentration on the bio-hydrogen production process. Lab bench scale anaerobic continuous stirred-tank reactors (CSTR were used to study the effect of substrate and sludge inoculation on hydrogen production. Three different concentrations of initial total volatile solids (TVS of organic waste were varied from 2%, 3% and 5% respectively. The pH was controlled at 5.5 for all batches in the experiment. The results showed that bio-hydrogen production depended on feed-substrate concentration. At initial TVS content of 3%, the highest hydrogen production was achieved at a level of 0.59 L-H2/L at pH 5.5. The maximum hydrogen yield was 15.3 ml H2/g TVS or 8.5 ml H2/g COD. The composition of H2 in the biogas ranged from 28.1-30.9% and no CH4 was detected in all batch tests.

  5. Hydrogen Production from Semiconductor-based Photocatalysis via Water Splitting

    Directory of Open Access Journals (Sweden)

    Jeffrey C. S. Wu

    2012-10-01

    Full Text Available Hydrogen is the ideal fuel for the future because it is clean, energy efficient, and abundant in nature. While various technologies can be used to generate hydrogen, only some of them can be considered environmentally friendly. Recently, solar hydrogen generated via photocatalytic water splitting has attracted tremendous attention and has been extensively studied because of its great potential for low-cost and clean hydrogen production. This paper gives a comprehensive review of the development of photocatalytic water splitting for generating hydrogen, particularly under visible-light irradiation. The topics covered include an introduction of hydrogen production technologies, a review of photocatalytic water splitting over titania and non-titania based photocatalysts, a discussion of the types of photocatalytic water-splitting approaches, and a conclusion for the current challenges and future prospects of photocatalytic water splitting. Based on the literatures reported here, the development of highly stable visible–light-active photocatalytic materials, and the design of efficient, low-cost photoreactor systems are the key for the advancement of solar-hydrogen production via photocatalytic water splitting in the future.

  6. Methane Pyrolysis for Hydrogen & Carbon Nanotube Recovery from Sabatier Products Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Development of a microgravity and hypogravity compatible catalytic methane pyrolysis reactor is proposed to recover hydrogen which is lost as methane in the...

  7. An assessment on hydrogen production using central receiver solar systems

    Science.gov (United States)

    Bilgen, C.; Bilgen, E.

    An assessment is presented on hydrogen production using a dedicated central receiver solar system concept coupled to two types of hydrogen producing processes, electrolysis and thermochemical. The study on solar electrolytic hydrogen was carried out using solar electricity and four different electrolytic technologies, namely, industrial unipolar 1980 and 1983 technologies, industrial bipolar and solid polymer electrolyte technology. The thermochemical process was the sulphur/iodine cycle, which is being developed by General Atomic Co. Systems, which is capable of producing about one-million GJ hydrogen per year, was developed at the conceptual level, and site specific computations were carried out. A general mathematical model was developed to predict the optical and thermal performance of the central receiver system coupled directly to the chemical plant. Cost models were developed for each subsystem based on the database published in the literature. Levelized and delevelized costs of solar hydrogen were then computed.

  8. Hydrogen production from wastewater sludge using a Clostridium strain.

    Science.gov (United States)

    Wang, C C; Chang, C W; Chu, C P; Lee, D J; Chang, B V; Liao, C S

    2003-09-01

    Limited data in literature revealed a relatively low hydrogen yield from wastewater sludge, ca. 0.16 mg/g-dried solids, using anaerobic fermentation. We demonstrated in this work a much higher hydrogen yield, around 1.1 mg-H2/g-dried solids using a clostridium strain isolated from the sludge sample. The formed hydrogen would be consumed after passing the peak value at around 30-36 h of fermentation. We examined the effects of employing five different pre-treatments on substrate sludge, but noted no appreciable enhancement in hydrogen yield as commonly expected for methane production. Since a vast amount of organic matters had been released to water after hydrogen fermentation, we externally dosed methanogenic bacteria to the fermented liquor to produce methane. The fermented liquor could produce more methane than the non-fermented sample, indicating that the dosed methanogenic bacteria readily utilized the organic matters derived from the fermentation test.

  9. Inter-esterified palm products as alternatives to hydrogenation.

    Science.gov (United States)

    Idris, Nor Aini; Dian, Noor Lida Habi Mat

    2005-01-01

    Inter-esterification is one of the processes used to modify the physico-chemical characteristics of oils and fats. Inter-esterification is an acyl-rearrangement reaction on the glycerol molecule. On the other hand, hydrogenation involves addition of hydrogen to the double bonds of unsaturated fatty acids. Due to health implications of trans fatty acids, which are formed during hydrogenation, the industry needs to find alternatives to hydrogenated fats. This paper discusses some applications of inter-esterified fats, with particular reference to inter-esterified palm products, as alternatives to hydrogenation. Some physico-chemical properties of inter-esterified fats used in shortenings are discussed. With inter-esterification, more palm stearin can be incorporated in vanaspati. For confectionary fats and infant formulations, enzymatic inter-esterification has been employed.

  10. Pyrolysis of de-oiled seed cake of Jatropha Curcas and catalytic steam reforming of pyrolytic bio-oil to hydrogen.

    Science.gov (United States)

    Renny, Andrew; Santhosh, Viswanathan; Somkuwar, Nitin; Gokak, D T; Sharma, Pankaj; Bhargava, Sanjay

    2016-11-01

    The aim of this work was to study the pyrolysis of de-oiled seed cake of Jatropha Curcas and catalytic steam reforming of pyrolytic bio-oil to hydrogen. As per literature, presence of heavy nitrogenous and oxygenated compounds leads to catalyst deactivation. Here, an attempt has been made to tune pyrolytic reactions to optimize the N and O content of the pyrolytic bio-oil. Bio-oil conversion and hydrogen yield decreased as reaction progressed, which attributes to temporary loss of catalytic activity by blockage of catalyst pores by carbon deposition. Further, retention of steam reforming activity after repetitive steam activation suggests long-term catalyst usage.

  11. Catalytic Hydrogenation of Methanol-Containing Eflfuent from Epoxidation of Propylene

    Institute of Scientific and Technical Information of China (English)

    Cheng Ke

    2015-01-01

    This paper describes the hydrogenation of impurities in the methanol-containing eflfuent from the propylene epoxidation process with hydrogen peroxide. The effects of reaction temperature, pressure, weight hourly space velocity (WHSV) and H2/methanol ratio on the concentration of various impurities in methanol solvent were investigated. It was found out that the aldehyde, hydrogen peroxide and nitro compounds in the methanol solvent could be completely hydroge-nated over the Ni catalyst under proper reaction conditions. 90%of acetone and up to 50%of acetals (ketals) existing in the methanol solvent could be hydrogenated. No signiifcant change was observed for the rest of the impurities that were present in the methanol solvent (i. e., 1-methoxy-2-propanol, 2-methoxy-1-propanol and 1,2-propanediol). The H2O2 decomposition reaction was enhanced using Ni catalyst, through the formation of NioOH, but no oxygen was found in the off-gas of hy-drogenation reaction since NioH could react on NioOH formed via dissociative adsorption of hydrogen peroxide, or on NioO formed via adsorption of oxygen.

  12. Using short pulses to enhance the production rate of vibrationally excited hydrogen molecules in hydrogen discharge

    Institute of Scientific and Technical Information of China (English)

    Sun Ji-Zhong; Li Xian-Tao; Bai Jing; Wang De-Zhen

    2012-01-01

    Hydrogen discharges driven by the combined radio-frequency(rf)/short pulse sources are investigated using the particle-in-cell method.The simulation results show that the discharge driven additionally by the short pulse can enhance the electron density and modulate the electron energy to provide a better condition for negative hydrogen ion production than the discharge driven by the rf-only source.

  13. Technoeconomic analysis of renewable hydrogen production, storage, and detection systems

    Energy Technology Data Exchange (ETDEWEB)

    Mann, M.K.; Spath, P.L.; Kadam, K. [National Renewable Energy Lab., Golden, CO (United States)

    1996-10-01

    Technical and economic feasibility studies of different degrees of completeness and detail have been performed on several projects being funded by the Department of Energy`s Hydrogen Program. Work this year focused on projects at the National Renewable Energy Laboratory, although analyses of projects at other institutions are underway or planned. Highly detailed analyses were completed on a fiber optic hydrogen leak detector and a process to produce hydrogen from biomass via pyrolysis followed by steam reforming of the pyrolysis oil. Less detailed economic assessments of solar and biologically-based hydrogen production processes have been performed and focused on the steps that need to be taken to improve the competitive position of these technologies. Sensitivity analyses were conducted on all analyses to reveal the degree to which the cost results are affected by market changes and technological advances. For hydrogen storage by carbon nanotubes, a survey of the competing storage technologies was made in order to set a baseline for cost goals. A determination of the likelihood of commercialization was made for nearly all systems examined. Hydrogen from biomass via pyrolysis and steam reforming was found to have significant economic potential if a coproduct option could be co-commercialized. Photoelectrochemical hydrogen production may have economic potential, but only if low-cost cells can be modified to split water and to avoid surface oxidation. The use of bacteria to convert the carbon monoxide in biomass syngas to hydrogen was found to be slightly more expensive than the high end of currently commercial hydrogen, although there are significant opportunities to reduce costs. Finally, the cost of installing a fiber-optic chemochromic hydrogen detection system in passenger vehicles was found to be very low and competitive with alternative sensor systems.

  14. Catalytic gasification of bagasse for the production of methanol

    Energy Technology Data Exchange (ETDEWEB)

    Baker, E.G.; Brown, M.D.; Robertus, R.J.

    1985-10-01

    The purpose of the study was to evaluate the technical and economic feasibility of catalytic gasification of bagasse to produce methanol. In previous studies, a catalytic steam gasification process was developed which converted wood to methanol synthesis gas in one step using nickel based catalysts in a fluid-bed gasifier. Tests in a nominal 1 ton/day process development unit (PDU) gasifier with these same catalysts showed bagasse to be a good feedstock for fluid-bed gasifiers, but the catalysts deactivated quite rapidly in the presence of bagasse. Laboratory catalyst screening tests showed K/sub 2/CO/sub 3/ doped on the bagasse to be a promising catalyst for converting bagasse to methanol synthesis gas. PDU tests with 10 wt % K/sub 2/CO/sub 3/ doped on bagasse showed the technical feasibility of this type of catalyst on a larger scale. A high quality synthesis gas was produced and carbon conversion to gas was high. The gasifier was successfully operated without forming agglomerates of catalyst, ash, and char in the gasifier. There was no loss of activity throughout the runs because catalysts is continually added with the bagasse. Laboratory tests showed about 80% of the potassium carbonate could be recovered and recycled with a simple water wash. An economic evaluation of the process for converting bagasse to methanol showed the required selling price of methanol to be significantly higher than the current market price of methanol. Several factors make this current evaluaton using bagasse as a feedstock less favorable: (1) capital costs are higher due to inflation and some extra costs required to use bagasse, (2) smaller plant sizes were considered so economies of scale are lost, and (3) the market price of methanol in the US has fallen 44% in the last six months. 24 refs., 14 figs., 16 tabs.

  15. Efficient catalytic interconversion between NADH and NAD+ accompanied by generation and consumption of hydrogen with a water-soluble iridium complex at ambient pressure and temperature.

    Science.gov (United States)

    Maenaka, Yuta; Suenobu, Tomoyoshi; Fukuzumi, Shunichi

    2012-01-11

    Regioselective hydrogenation of the oxidized form of β-nicotinamide adenine dinucleotide (NAD(+)) to the reduced form (NADH) with hydrogen (H(2)) has successfully been achieved in the presence of a catalytic amount of a [C,N] cyclometalated organoiridium complex [Ir(III)(Cp*)(4-(1H-pyrazol-1-yl-κN(2))benzoic acid-κC(3))(H(2)O)](2) SO(4) [1](2)·SO(4) under an atmospheric pressure of H(2) at room temperature in weakly basic water. The structure of the corresponding benzoate complex Ir(III)(Cp*)(4-(1H-pyrazol-1-yl-κN(2))-benzoate-κC(3))(H(2)O) 2 has been revealed by X-ray single-crystal structure analysis. The corresponding iridium hydride complex formed under an atmospheric pressure of H(2) undergoes the 1,4-selective hydrogenation of NAD(+) to form 1,4-NADH. On the other hand, in weakly acidic water the complex 1 was found to catalyze the hydrogen evolution from NADH to produce NAD(+) without photoirradiation at room temperature. NAD(+) exhibited an inhibitory behavior in both catalytic hydrogenation of NAD(+) with H(2) and H(2) evolution from NADH due to the binding of NAD(+) to the catalyst. The overall catalytic mechanism of interconversion between NADH and NAD(+) accompanied by generation and consumption of H(2) was revealed on the basis of the kinetic analysis and detection of the catalytic intermediates.

  16. Bacterial bioaugmentation for improving methane and hydrogen production from microalgae

    Science.gov (United States)

    2013-01-01

    Background The recalcitrant cell walls of microalgae may limit their digestibility for bioenergy production. Considering that cellulose contributes to the cell wall recalcitrance of the microalgae Chlorella vulgaris, this study investigated bioaugmentation with a cellulolytic and hydrogenogenic bacterium, Clostridium thermocellum, at different inoculum ratios as a possible method to improve CH4 and H2 production of microalgae. Results Methane production was found to increase by 17?~?24% with the addition of C. thermocellum, as a result of enhanced cell disruption and excess hydrogen production. Furthermore, addition of C. thermocellum enhanced the bacterial diversity and quantities, leading to higher fermentation efficiency. A two-step process of addition of C. thermocellum first and methanogenic sludge subsequently could recover both hydrogen and methane, with a 9.4% increase in bioenergy yield, when compared with the one-step process of simultaneous addition of C. thermocellum and methanogenic sludge. The fluorescence peaks of excitation-emission matrix spectra associated with chlorophyll can serve as biomarkers for algal cell degradation. Conclusions Bioaugmentation with C. thermocellum improved the degradation of C. vulgaris biomass, producing higher levels of methane and hydrogen. The two-step process, with methanogenic inoculum added after the hydrogen production reached saturation, was found to be an energy-efficiency method for hydrogen and methane production. PMID:23815806

  17. Activating basal-plane catalytic activity of two-dimensional MoS2 monolayer with remote hydrogen plasma

    KAUST Repository

    Cheng, Chia-Chin

    2016-09-10

    Two-dimensional layered transition metal dichalcogenide (TMD) materials such as Molybdenum disufide (MoS2) have been recognized as one of the low-cost and efficient electrocatalysts for hydrogen evolution reaction (HER). The crystal edges that account for a small percentage of the surface area, rather than the basal planes, of MoS2 monolayer have been confirmed as their active catalytic sites. As a result, extensive efforts have been developing in activating the basal planes of MoS2 for enhancing their HER activity. Here, we report a simple and efficient approach-using a remote hydrogen-plasma process-to creating S-vacancies on the basal plane of monolayer crystalline MoS2; this process can generate high density of S-vacancies while mainly maintaining the morphology and structure of MoS2 monolayer. The density of S-vacancies (defects) on MoS2 monolayers resulted from the remote hydrogen-plasma process can be tuned and play a critical role in HER, as evidenced in the results of our spectroscopic and electrical measurements. The H2-plasma treated MoS2 also provides an excellent platform for systematic and fundamental study of defect-property relationships in TMDs, which provides insights for future applications including electrical, optical and magnetic devices. © 2016 Elsevier Ltd.

  18. Protons and pleomorphs: aerobic hydrogen production in Azotobacters.

    Science.gov (United States)

    Noar, Jesse D; Bruno-Bárcena, José M

    2016-02-01

    As obligate aerobic soil organisms, the ability of Azotobacter species to fix nitrogen is unusual given that the nitrogenase complex requires a reduced cellular environment. Molecular hydrogen is an unavoidable byproduct of the reduction of dinitrogen; at least one molecule of H2 is produced for each molecule of N2 fixed. This could be considered a fault in nitrogenase efficiency, essentially a waste of energy and reducing equivalents. Wild-type Azotobacter captures this hydrogen and oxidizes it with its membrane-bound uptake hydrogenase complex. Strains lacking an active hydrogenase complex have been investigated for their hydrogen production capacities. What is the role of H2 in the energy metabolism of nitrogen-fixing Azotobacter? Is hydrogen production involved in Azotobacter species' protection from or tolerance to oxygen, or vice versa? What yields of hydrogen can be expected from hydrogen-evolving strains? Can the yield of hydrogen be controlled or increased by changing genetic, environmental, or physiological conditions? We will address these questions in the following mini-review.

  19. Room Temperature Reactivity Of Silicon Nanocrystals With Solvents: The Case Of Ketone And Hydrogen Production From Secondary Alcohols: Catalysis?

    KAUST Repository

    El Demellawi, Jehad K.

    2015-05-29

    Although silicon nanoparticles dispersed in liquids are used in various applications ranging from bio-labeling to hydrogen production, their reactivities with their solvents and their catalytic properties re-main still unexplored. Here, we discovered that, because of their surface structures and mechanical strain, silicon nanoparticles react strongly with their solvents and may act as catalysts for the dehydrogenation, at room temperature, of secondary alcohols (e.g. isopropanol) to ketones and hydrogen. This catalytic reaction was followed by gas chromatography, pH measurements, mass spectroscopy and solidstate NMR. This discovery provides new understanding of the role played by silicon nanoparticles, and nanosilicon in general, in their stability in solvents in general as well as being candidates in catalysis.

  20. Hydrogen production from the steam reforming of bio-butanol over novel supported Co-based bimetallic catalysts.

    Science.gov (United States)

    Cai, Weijie; de la Piscina, Pilar Ramirez; Homs, Narcis

    2012-03-01

    This paper reports the hydrogen production through the steam reforming of a bioresource-derived butanol mixture (butanol:acetone:ethanol=6:3:1 mass ratio) over supported cobalt-based catalysts. The support plays an important role for the catalytic behavior and Co/ZnO exhibits the best catalytic performance compared to Co/TiO(2) and Co/CeO(2). Moreover, a higher hydrogen yield is obtained over bimetallic Co-Ir/ZnO, which shows an increase in H(2) selectivity and a decrease in CH(4) selectivity under steam reforming conditions, compared to Co/ZnO. Raman results of the used catalysts indicate that the addition of Ir could prevent the coke formation to prolong the catalyst stability.

  1. Identification of intrinsic catalytic activity for electrochemical reduction of water molecules to generate hydrogen

    KAUST Repository

    Shinagawa, Tatsuya

    2015-01-01

    Insufficient hydronium ion activities at near-neutral pH and under unbuffered conditions induce diffusion-limited currents for hydrogen evolution, followed by a reaction with water molecules to generate hydrogen at elevated potentials. The observed constant current behaviors at near neutral pH reflect the intrinsic electrocatalytic reactivity of the metal electrodes for water reduction. This journal is © the Owner Societies.

  2. Hydrogen Production Costs of Various Primary Energy Sources

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Jae Hyuk; Tak, Nam Il; Kim, Yong Hee; Park, Won Seok

    2005-11-15

    Many studies on the economical aspects of hydrogen energy technologies have been conducted with the increase of the technical and socioeconomic importance of the hydrogen energy. However, there is still no research which evaluates the economy of hydrogen production from the primary energy sources in consideration of Korean situations. In this study, the hydrogen production costs of major primary energy sources are compared in consideration of the Korean situations such as feedstock price, electricity rate, and load factor. The evaluation methodology is based on the report of the National Academy of Science (NAS) of U.S. The present study focuses on the possible future technology scenario defined by NAS. The scenario assumes technological improvement that may be achieved if present research and development (R and D) programs are successful. The production costs by the coal and natural gas are 1.1 $/kgH{sub 2} and 1.36 $/kgH{sub 2}, respectively. However, the fossil fuels are susceptible to the price variation depending on the oil and the raw material prices, and the hydrogen production cost also depends on the carbon tax. The economic competitiveness of the renewable energy sources such as the wind, solar, and biomass are relatively low when compared with that of the other energy sources. The estimated hydrogen production costs from the renewable energy sources range from 2.35 $/kgH{sub 2} to 6.03 $/kgH{sub 2}. On the other hand, the production cost by nuclear energy is lower than that of natural gas or coal when the prices of the oil and soft coal are above $50/barrel and 138 $/ton, respectively. Taking into consideration the recent rapid increase of the oil and soft coal prices and the limited fossil resource, the nuclear-hydrogen option appears to be the most economical way in the future.

  3. A homogeneous transition metal complex for clean hydrogen production from methanol-water mixtures

    Science.gov (United States)

    Rodríguez-Lugo, Rafael E.; Trincado, Mónica; Vogt, Matthias; Tewes, Friederike; Santiso-Quinones, Gustavo; Grützmacher, Hansjörg

    2013-04-01

    The development of an efficient catalytic process that mimics the enzymatic function of alcohol dehydrogenase is critical for using biomass alcohols for both the production of H2 as a chemical energy carrier and fine chemicals under waste-free conditions. Dehydrogenation of alcohol-water mixtures into their corresponding acids with molecular hydrogen as the sole by-product from the reaction can be catalysed by a ruthenium complex with a chelating bis(olefin) diazadiene ligand. This complex, [K(dme)2][Ru(H)(trop2dad)], stores up to two equivalents of hydrogen intramolecularly, and catalyses the production of H2 from alcohols in the presence of water and a base under homogeneous conditions. The conversion of a MeOH-H2O mixture proceeds selectively to CO2/H2 gas formation under neutral conditions, thereby allowing the use of the entire hydrogen content (12% by weight). Isolation and characterization of the ruthenium complexes from these reactions suggested a mechanistic scenario in which the trop2dad ligand behaves as a chemically ‘non-innocent’ co-operative ligand.

  4. A homogeneous transition metal complex for clean hydrogen production from methanol-water mixtures.

    Science.gov (United States)

    Rodríguez-Lugo, Rafael E; Trincado, Mónica; Vogt, Matthias; Tewes, Friederike; Santiso-Quinones, Gustavo; Grützmacher, Hansjörg

    2013-04-01

    The development of an efficient catalytic process that mimics the enzymatic function of alcohol dehydrogenase is critical for using biomass alcohols for both the production of H2 as a chemical energy carrier and fine chemicals under waste-free conditions. Dehydrogenation of alcohol-water mixtures into their corresponding acids with molecular hydrogen as the sole by-product from the reaction can be catalysed by a ruthenium complex with a chelating bis(olefin) diazadiene ligand. This complex, [K(dme)2][Ru(H)(trop2dad)], stores up to two equivalents of hydrogen intramolecularly, and catalyses the production of H2 from alcohols in the presence of water and a base under homogeneous conditions. The conversion of a MeOH-H2O mixture proceeds selectively to CO2/H2 gas formation under neutral conditions, thereby allowing the use of the entire hydrogen content (12% by weight). Isolation and characterization of the ruthenium complexes from these reactions suggested a mechanistic scenario in which the trop2dad ligand behaves as a chemically 'non-innocent' co-operative ligand.

  5. Discovery of Photocatalysts for Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    D. Brent MacQueen

    2006-10-01

    This project for DOE was designed to address these materials-related issues through a combination of high-throughput screening of semiconductor candidates and theoretical modeling of nanostructures. High-throughput screening is an effective and economical way to examine a large number of candidates and identify those worthy of further study. Unfortunately, in the course of this project, we discovered no semiconductor candidates that can meet the DOE’s stringent requirements for an economically feasible photoelectrochemical process. However, some of our results indicated that several systems may have potential if further optimized. In particular, the published theoretical modeling work indicates that core-shell nanorod structures, if properly engineered, have the potential to overcome the shortfalls of current semiconductors. Although the synthesis of the designed core-shell nanorod structures proved to be beyond the current capabilities of our laboratories, recent advances in the synthesis of core-shell nanorod structures imply that the designed structures can be synthesized. SRI is confident that once these materials are made they will validate our models and lead to economical and environmentally friendly hydrogen from sunlight and water. The high-throughput photolysis analysis module developed at SRI will also have utility in applications such as identifying catalysts for photo-assisted chemical detoxification, as well as non-photolytic applications such as hydrogen storage, which can take advantage of the ability of the analysis module to monitor pressure over time.

  6. Effect of inoculum conditioning on hydrogen fermentation and pH effect on bacterial community relevant to hydrogen production.

    Science.gov (United States)

    Kawagoshi, Yasunori; Hino, Naoe; Fujimoto, Aya; Nakao, Masaharu; Fujita, Yukiko; Sugimura, Seiji; Furukawa, Kenji

    2005-11-01

    The effect of conditioning for a variety of inoculums on fermentative hydrogen production was investigated. In addition, the effects of pH condition on hydrogen fermentation and bacterial community were investigated. The effect of conditioning on hydrogen production was different depending on the inoculum types. An appreciable hydrogen production was shown with anaerobic digested sludge and lake sediment without conditioning, however, no hydrogen was produced when refuse compost and kiwi grove soil were used as inoculums without conditioning. The highest hydrogen production was obtained with heat-conditioned anaerobic digested sludge, almost the same production was also obtained with unconditioned digested sludge. The pH condition considerably affected hydrogen fermentation, hydrogen gas was efficiently produced with unconditioned anaerobic sludge when the pH was controlled at 6.0 throughout the culture period and not when only the initial pH was adjusted to 6.0 and 7.0. Hydrogen production decreased when the culture pH was only adjusted at the beginning of each batch in continuous batch culture, and additionally, bacterial community varied with the change in hydrogen production. It was suggested that Clostridium and Coprothermobacter species played important role in hydrogen fermentation, and Lactobacillus species had an adverse effect on hydrogen production.

  7. Unsteady catalytic processes and sorption-catalytic technologies

    Energy Technology Data Exchange (ETDEWEB)

    Zagoruiko, A N [G.K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Novosibirsk (Russian Federation)

    2007-07-31

    Catalytic processes that occur under conditions of the targeted unsteady state of the catalyst are considered. The highest efficiency of catalytic processes was found to be ensured by a controlled combination of thermal non-stationarity and unsteady composition of the catalyst surface. The processes based on this principle are analysed, in particular, catalytic selective reduction of nitrogen oxides, deep oxidation of volatile organic impurities, production of sulfur by the Claus process and by hydrogen sulfide decomposition, oxidation of sulfur dioxide, methane steam reforming and anaerobic combustion, selective oxidation of hydrocarbons, etc.

  8. Microbial production of hydrogen from starch-manufacturing wastes

    Energy Technology Data Exchange (ETDEWEB)

    Yokoi, H.; Maki, R.; Hirose, J.; Hayashi, S. [Miyazaki Univ. (Japan). Dept. of Applied Chemistry

    2002-05-01

    Effective hydrogen production from starch-manufacturing wastes by microorganisms was investigated. Continuous hydrogen production in high yield of 2.7 mol H{sub 2} mol{sup -1} glucose was attained by a mixed culture of Clostridium butyricum and Enterobacter aerogenes HO-39 in the starch waste medium consisting of sweet potato starch residue as a carbon source and corn steep liquor as a nitrogen source in a repeated batch culture. Rhodobacter sp. M-19 could produce hydrogen from the supernatant of the culture broth obtained in the repeated batch culture of C. butyricum and E. aerogenes HO-39. Hydrogen yield of 4.5 mol H{sub 2} mol{sup -1} glucose was obtained by culturing Rhodobacter sp. M-19 in the supernatant supplemented with 20{mu}gl{sup -1} Na{sub 2}MoO{sub 4} 2H{sub 2}O and 10mgl{sup -1} EDTA in a repeated batch culture with pH control at 7.5. Therefore, continuous hydrogen production with total hydrogen yield of 7.2 mol H{sub 2} mol{sup -1} glucose from the starch remaining in the starch residue was attained by the repeated batch culture with C. butyricum and E. aerogenes HO-39 and by the successive repeated batch culture with Rhodobacter sp. M-19. (Author)

  9. Engineering analysis of potential photosynthetic bacterial hydrogen-production systems

    Science.gov (United States)

    Herlevich, A.; Karpuk, M. E.

    1982-06-01

    Photosynthetic bacteria (PSB) are capable of generating hydrogen from organics in effluents from food processing, pulp and paper, and chemical and pharmaceutical industries. Hydrogen evolution takes place under light in the absence of air. The rate of hydrogen production is expected to range between 300 to 600 scf of hydrogen per 1000 galloons of waste stream treated per hour. This hydrogen production system has been demonstrated at a bench-scale level and is ready for engineering development. A conceptual design for a PSB hydrogen production system is described. The system is expected to be sited adjacent to a waste stream source which will be pretreated by fermentation and pH adjustment, innoculated with bacteria, and then passed into the reactor. The reactor effluent can either be discharged into a rapid infiltration system, an irrigation ditch, and/or recycled back into the reactor. Several potential reactor designs have been developed, analyzed, and costed. A large covered pond appears to be the most economical design approach.

  10. Hydrogen production and storage: R & D priorities and gaps

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2006-05-04

    This review of priorities and gaps in hydrogen production and storage R & D has been prepared by the IEA Hydrogen Implementing Agreement in the context of the activities of the IEA Hydrogen Co-ordination Group. It includes two papers. The first is by Trygve Riis, Elisabet F. Hagen, Preben J.S. Vie and Oeystein Ulleberg. This offers an overview of the technologies for hydrogen production. The technologies discussed are reforming of natural gas; gasification of coal and biomass; and the splitting of water by water-electrolysis, photo-electrolysis, photo-biological production and high-temperature decomposition. The second paper is by Trygve Riis, Gary Sandrock, Oeystein Ulleberg and Preben J.S. Vie. The objective of this paper is to provide a brief overview of the possible hydrogen storage options available today and in the foreseeable future. Hydrogen storage can be considered for onboard vehicular, portable, stationary, bulk, and transport applications, but the main focus of this paper is on vehicular storage, namely fuel cell or ICE/electric hybrid vehicles. 7 refs., 24 figs., 14 tabs.

  11. Photosynthetic hydrogen and oxygen production by green algae

    Energy Technology Data Exchange (ETDEWEB)

    Greenbaum, E.; Lee, J.W.

    1997-12-31

    An overview of photosynthetic hydrogen and oxygen production by green algae in the context of its potential as a renewable chemical feed stock and energy carrier is presented. Beginning with its discovery by Gaffron and Rubin in 1942, motivated by curiosity-driven laboratory research, studies were initiated in the early 1970s that focused on photosynthetic hydrogen production from an applied perspective. From a scientific and technical point of view, current research is focused on optimizing net thermodynamic conversion efficiencies represented by the Gibbs Free Energy of molecular hydrogen. The key research questions of maximizing hydrogen and oxygen production by light-activated water splitting in green algae are (1) removing the oxygen sensitivity of algal hydrogenases; (2) linearizing the light saturation curves of photosynthesis throughout the entire range of terrestrial solar irradiance--including the role of bicarbonate and carbon dioxide in optimization of photosynthetic electron transport and (3) the minimum number of light reactions that are required to split water to elemental hydrogen and oxygen. Each of these research topics is being actively addressed by the photobiological hydrogen research community.

  12. Kinetic study of biological hydrogen production by anaerobic fermentation

    Energy Technology Data Exchange (ETDEWEB)

    Sangeetha, R. [Annamalai Univ., Chidambaram (India). Dept. of Chemical Engineering; Karunanithi, T. [Annamalai Univ., Tamilnadu (India). Dept. of Chemical Engineering

    2009-07-01

    This study examined the kinetics of batch biohydrogen production from glucose. Clostridium pasteurianum was used to produce biohydrogen by dark anaerobic fermentation. The initial substrate concentration, initial pH and temperature were optimized for biohydrogen production. The maximum production of hydrogen under optimum conditions was found to be 5.376 l/l. The kinetic parameters were determined for the optimized medium and conditions in the batch reactor. The by product was expressed as total acidic equivalent. This presentation discussed the logistic equation that was used to model the growth of the organism and described how the kinetic parameters were calculated. The Leudeking piret kinetic model was used to express the hydrogen production and substrate use because it combines both growth associated and non associated contributions. It was concluded the production of biohydrogen can be predicted well using the logistic model for cell growth kinetics and the logistic incorporated Leudeking Piret model for product and substrate utilization kinetics.

  13. EVermont Renewable Hydrogen Production and Transportation Fueling System

    Energy Technology Data Exchange (ETDEWEB)

    Garabedian, Harold T.

    2008-03-30

    A great deal of research funding is being devoted to the use of hydrogen for transportation fuel, particularly in the development of fuel cell vehicles. When this research bears fruit in the form of consumer-ready vehicles, will the fueling infrastructure be ready? Will the required fueling systems work in cold climates as well as they do in warm areas? Will we be sure that production of hydrogen as the energy carrier of choice for our transit system is the most energy efficient and environmentally friendly option? Will consumers understand this fuel and how to handle it? Those are questions addressed by the EVermont Wind to Wheels Hydrogen Project: Sustainable Transportation. The hydrogen fueling infrastructure consists of three primary subcomponents: a hydrogen generator (electrolyzer), a compression and storage system, and a dispenser. The generated fuel is then used to provide transportation as a motor fuel. EVermont Inc., started in 1993 by then governor Howard Dean, is a public-private partnership of entities interested in documenting and advancing the performance of advanced technology vehicles that are sustainable and less burdensome on the environment, especially in areas of cold climates, hilly terrain and with rural settlement patterns. EVermont has developed a demonstration wind powered hydrogen fuel producing filling system that uses electrolysis, compression to 5000 psi and a hydrogen burning vehicle that functions reliably in cold climates. And that fuel is then used to meet transportation needs in a hybrid electric vehicle whose internal combustion engine has been converted to operate on hydrogen Sponsored by the DOE EERE Hydrogen, Fuel Cells & Infrastructure Technologies (HFC&IT) Program, the purpose of the project is to test the viability of sustainably produced hydrogen for use as a transportation fuel in a cold climate with hilly terrain and rural settlement patterns. Specifically, the project addresses the challenge of building a renewable

  14. Hydrogen production through aqueous-phase reforming of ethylene glycol in a washcoated microchannel.

    Science.gov (United States)

    D'Angelo, M Fernanda Neira; Ordomsky, Vitaly; Paunovic, Violeta; van der Schaaf, John; Schouten, Jaap C; Nijhuis, T Alexander

    2013-09-01

    Aqueous-phase reforming (APR) of biocarbohydrates is conducted in a catalytically stable washcoated microreactor where multiphase hydrogen removal enhances hydrogen efficiency. Single microchannel experiments are conducted following a simplified model based on the microreactor concept. A coating method to deposit a Pt-based catalyst on the microchannel walls is selected and optimized. APR reactivity tests are performed by using ethylene glycol as the model compound. Optimum results are achieved with a static washcoating technique; a highly uniform and well adhered 5 μm layer is deposited on the walls of a 320 μm internal diameter (ID) microchannel in one single step. During APR of ethylene glycol, the catalyst layer exhibits high stability over 10 days after limited initial deactivation. The microchannel presents higher conversion and selectivity to hydrogen than a fixed-bed reactor. The benefits of using a microreactor for APR can be further enhanced by utilizing increased Pt loadings, higher reaction temperatures, and larger carbohydrates (e.g., glucose). The use of microtechnology for aqueous-phase reforming will allow for a great reduction in the reformer size, thus rendering it promising for distributed hydrogen production.

  15. Renewable energy from biomass: a sustainable option? - Hydrogen production from alcohols

    Science.gov (United States)

    Balla, Zoltán; Kith, Károly; Tamás, András; Nagy, Orsolya

    2015-04-01

    in the case, than the same volume of ethanol-water mixture can be prepared. The renewal of alcohol, the alcohol-water mixture is then passed through the catalytic reformer into a preheater. The exhaust gas contains a relatively large number of carbon monoxide, which would spoil the fuel cell, so the carbon monoxide concentration to a high and a low temperature water-gas reaction is reduced. This increases the hydrogen production. The last step of the carbon monoxide content to eliminate preferential oxidation. The alcohol reforming catalyst for the precious metals spread most of what arose from high activity and stability. However, the precious metals are very expensive, so a non-precious metal catalysts is the design and development of objective activity and stability which reaches the precious metal catalysts of. Using the new reaction catalysts opportunities are created, which are smaller than the activation energy than the non-catalytic process. The basic objective of the technological developments more active at lower temperatures, the selective target product, long-life, low cost design catalysts.

  16. Novel Catalytic Materials and Strategies for Hydrogen Production and Hydrogenation Reactions based on PEM Electrolysis

    OpenAIRE

    Ampurdanés Vilanova, Jordi

    2014-01-01

    La producción de hidrógeno, a gran escala, a partir de agua se ha convertido en un reto desde ya hace unos cuantos años. Así, una vía ecológica y eficiente para la generación de hidrógeno tiene que establecerse. Entre todas las posibilidades, electrólisis mediante la tecnología de membranas de intercambio de protones (PEM) es la técnica más prometedora para conseguir dicho propósito. Además, dicha aproximación también puede ser considerada para llevar a cabo otras reacciones electroquímicas c...

  17. Synergic catalytic effect of Ti hydride and Nb nanoparticles for improving hydrogenation and dehydrogenation kinetics of Mg-based nanocomposite

    Directory of Open Access Journals (Sweden)

    Xiujuan Ma

    2017-02-01

    Full Text Available The Mg-9.3 wt% (TiH1.971-TiH−0.7 wt% Nb nanocomposite has been synthesized by hydrogen plasma-metal reaction (HPMR approach to enhance the hydrogen sorption kinetics of Mg at moderate temperatures by providing nanosizing effect of increasing H “diffusion channels” and adding transition metallic catalysts. The Mg nanoparticles (NPs were in hexagonal shape range from 50 to 350 nm and the average size of the NPs was 177 nm. The small spherical TiH1.971, TiH and Nb NPs of about 25 nm uniformly decorated on the surface of the big Mg NPs. The Mg-TiH1.971-TiH-Nb nanocomposite could quickly absorb 5.6 wt% H2 within 5 min at 573 K and 4.5 wt% H2 within 5 min at 523 K, whereas the pure Mg prepared by HPMR could only absorb 4 and 1.5 wt% H2 at the same temperatures. TiH1.971, TiH and Nb NPs transformed into TiH2 and NbH during hydrogenation and recovered after dehydrogenation process. The apparent activation energies of the nanocomposite for hydrogenation and dehydrogenation were 45.0 and 50.7 kJ mol−1, which are much smaller than those of pure Mg NPs, 123.8 and 127.7 kJ mol−1. The improved sorption kinetics of the Mg-based nanocomposite at moderate temperatures and the small activation energy can be interpreted by the nanostructure of Mg and the synergic catalytic effects of Ti hydrides and Nb NPs.

  18. Photovoltaic hydrogen production with commercial alkaline electrolysers

    Energy Technology Data Exchange (ETDEWEB)

    Ursua, A.; Lopez, J.; Gubia, E.; Marroyo, L.; Sanchis, P. [Public Univ. of Navarra, Pamplona (Spain). Dept. of Electric and Electronic Engineering

    2010-07-01

    Renewable energy sources and Electrolysis generate the so-called green Hydrogen, a zero-emission and potentially fossil fuel independent energy source. However, the inherent variability of the renewable energy sources implies a mode of operation for which most current electrolysers have not been designed. This paper analyses the operation of a water electrolyser fed with photovoltaic (PV) generator electric profile. The system, Integrated by a 1 Nm{sup 3}/h Hydrogenics alkaline electrolyser and a 5100 W PV generator with 60 BP585 modules, is installed at the Public University of Navarra (Spain). The PV generator profile fed to the electrolyser is emulated by a custom-made apparatus designed and built by the authors of this paper. The profile is designed according to real irradiance data measured by a calibration cell. The irradiance data are converted to the electric power profile that the PV generator would have delivered in case of having been connected to the electrolyser by means of a DC/DC converter with maximum power point tracking (MPPT). Finally, from previously measured power-current electrolyser characteristic curves, the current profile to be delivered to the electrolyser is obtained and programmed to the electronic device. The electrolyser was tested for two types of days. During the first day, the irradiance was very stable, whereas during the second day, the irradiance was very variable. The experimental results show an average power consumption rate and an efficiency of 4908 Wh/Nm{sup 3} and 72.1%, on the first day, and 4842 Wh/Nm{sup 3} and 73.3% on the second day. The electrolyser performance was particularly good in spite of the high variability of the electric supply of the second day. (orig.)

  19. Study on biomass catalytic pyrolysis for production of bio-gasoline by on-line FTIR

    Institute of Scientific and Technical Information of China (English)

    Chang Bo Lu; Jian Zhong Yao; Wei Gang Lin; Wen Li Song

    2007-01-01

    The pyrolysis of biomass is a promising way for production of bio-gasoline if the stability and quality problems of the bio-crudeoil can be solved by catalytic cracking and reforming. In this paper, an on-line infrared spectrum was used to study the characteristics of catalytic pyrolysis with the following preliminary results. The removal of C=O of organic acid is more difficult than that of aldehydes and ketones. HUSY/γ-Al2O3 and REY/γ-Al2O3 catalysts exhibited better deoxygenating activities while HZSM-5/γ-Al2O3 catalyst exhibited preferred selectivities for production of iso-alkanes and aromatics. Finally, possible mechanisms of biomass catalytic pyrolysis are discussed as well.

  20. Size Control of Iron Oxide Nanoparticles Using Reverse Microemulsion Method: Morphology, Reduction, and Catalytic Activity in CO Hydrogenation

    Directory of Open Access Journals (Sweden)

    Mohammad Reza Housaindokht

    2013-01-01

    Full Text Available Iron oxide nanoparticles were prepared by microemulsion method and evaluated in Fischer-Tropsch synthesis. The precipitation process was performed in a single-phase microemulsion operating region. Different HLB values of surfactant were prepared by mixing of sodium dodecyl sulfate (SDS and Triton X-100. Transmission electron microscopy (TEM, surface area, pore volume, average pore diameter, pore size distribution, and XRD patterns were used to analyze size distribution, shape, and structure of precipitated hematite nanoparticles. Furthermore, temperature programmed reduction (TPR and catalytic activity in CO hydrogenation were implemented to assess the performance of the samples. It was found that methane and CO2 selectivity and also the syngas conversion increased as the HLB value of surfactant decreased. In addition, the selectivity to heavy hydrocarbons and chain growth probability (α decreased by decreasing the catalyst crystal size.

  1. Synthesis and Catalytic Performance of Ni/SiO2 for Hydrogenation of 2-Methylfuran to 2-Methyltetrahydrofuran

    Directory of Open Access Journals (Sweden)

    Fu Ding

    2015-01-01

    Full Text Available A series of Ni/SiO2 catalysts with different Ni content were prepared by sol-gel method for application in the synthesis of 2-methyltetrahydrofuran (2-MTHF by hydrogenation of 2-methylfuran (2-MF. The catalyst structure was investigated by X-ray diffraction (XRD, transmission electron microscopy (TEM, X-ray photoelectron spectroscopy (XPS, and temperature programmed reduction (TPR. It is found that structures and catalytic performance of the catalysts were highly affected by the Ni content. The catalyst with a 25% Ni content had an appropriate size of the Ni species and larger BET surface area and produced a higher 2-MF conversion with enhanced selectivity in 2-MTHF.

  2. Preparation and Characterization of A New Dinuclear Ruthenium Complex with BDPX Ligand and Its Catalytic Hydrogenation Reactions for Cinnamaldehyde

    Institute of Scientific and Technical Information of China (English)

    TANG,Yuan-You(唐元友); LI,Rui-Xiang(李瑞祥); LI,Xian-Jun(李贤均); WONG,Ning-Bew(黄宁表); TIN,Kim-Chung(田金忠); ZHANG,Zhe-Ying(张哲英); MAK,Thomas C.W.(麦松威)

    2004-01-01

    A new anionic dinuclear ruthenium complex bearing 1,2-bis(diphenylphosphinomethyl)benzene (BDPX)[NH2Et2][{RuCl (BDPX)}2(μ-Cl)3] (1) was synthesized and its structure was determined by an X-ray crystallographic analysis. This result indicated that complex 1 consisted of an anion dinuclear BDPX-Ru and a cationic diethylammonium. The crystal belonged to monoclinic system, C2/c space group with a=3.3552(7) nm, b= 1.8448(4)nm, c=2.4265(5) nm, β= 101.89(3)° and Z=8. The catalytic hydrogenation activities and selectivities of complex 1 for cinnamaldehyde were investigated.

  3. Media Improvement for Hydrogen Production Using C. acetobutylicum NCIMB 13357

    Directory of Open Access Journals (Sweden)

    Mohd S. Kalil

    2009-01-01

    Full Text Available Problem statement: Some component of fermentation medium showed to reduce the bacterial production of hydrogen. Approach: Reinforced clostridium medium is a selected medium for Clostridium species. Reformulation this medium regarding hydrogen production may focus on such medium composition that enhance or reduce the bacterial productivity. The optimum pH and temperature for hydrogen production were at initial pH of 7.0 and 30°C. Results: The results show that both nitrogen source and its concentration affected biomass growth as well as H2 yield. Yeast extract at concentration of 13 gL-1 was the best organic nitrogen source and resulted in hydrogen yield (YP/S of 308 mL g-1 glucose utilized with biomass concentration of 1.1 gL-1, hydrogen yield per biomass (YP/X of 280 mL g-1 L-1, biomass per substrate utilized (YX/S of 0.22 and produced hydrogen in gram per gram of glucose utilized (YH2/S of 0.0275. C/N of 70 enhanced the YP/S from 308 mL g-1 to 350 mL g-1 glucose utilized with biomass concentration of 1.22 gL-1, YP/X of 287 mL g-1 L-1, YX/S of 0.244 and (YH2/S of 0.03125. In the absence of sodium chloride and sodium acetate further enhanced YP/S from 350 mL g-1 glucose utilized to 391 mL g-1 glucose utilized with maximum hydrogen productivity of 77.5 mL L-1 h-1, whereas RCM medium gave the highest hydrogen productivity of 63.5 mL L-1h-1. Results also show that Sodium Chloride and Sodium Acetate in the medium adversely affect growth. Removal of both components from the medium enhanced the biomass concentration from 1.22-1.34 gL-1, YP/X of 254 mL g-1 L-1, YX/S of 0.268 and (YH2/S of 0.0349. Conclusion: The medium an improved containing (glucose 5 gL-1, Yeast extract gL-1, L-Cystine. HCl 1 gL-1 and Bacteriological agar 0.5 gL-1, was able to enhance the hydrogen productivity.

  4. Effect of ozone pretreatment on hydrogen production from barley straw.

    Science.gov (United States)

    Wu, Jiangning; Ein-Mozaffari, Farhad; Upreti, Simant

    2013-09-01

    Application of ozone technology to lignocellulosic biohydrogen production was explored with a barley straw. Ozone pretreatment effectively degraded the straw lignin and increased reducing sugar yield. A simultaneous enzyme hydrolysis and dark fermentation experiment was conducted using a mixed anaerobic consortium together with saccharification enzymes. Both untreated and ozonated samples produced hydrogen. Compared to the untreated group, hydrogen produced by the groups ozonated for 15, 30, 45 and 90 min increased 99%, 133%, 166% and 94%, respectively. Some inhibitory effect on hydrogen production was observed with the samples ozonated for 90 min, and the inhibition was on the fermentative microorganisms, not the saccharification enzymes. These results demonstrate that production of biohydrogen from barley straw, a lignocellulosic biomass, can be significantly enhanced by ozone pretreatment.

  5. Catalytic activity of Pd-doped Cu nanoparticles for hydrogenation as a single-atom-alloy catalyst.

    Science.gov (United States)

    Cao, Xinrui; Fu, Qiang; Luo, Yi

    2014-05-14

    The single atom alloy of extended surfaces is known to provide remarkably enhanced catalytic performance toward heterogeneous hydrogenation. Here we demonstrate from first principles calculations that this approach can be extended to nanostructures, such as bimetallic nanoparticles. The catalytic properties of the single-Pd-doped Cu55 nanoparticles have been systemically examined for H2 dissociation as well as H atom adsorption and diffusion, following the concept of single atom alloy. It is found that doping a single Pd atom at the edge site of the Cu55 shell can considerably reduce the activation energy of H2 dissociation, while the single Pd atom doped at the top site or in the inner layers is much less effective. The H atom adsorption on Cu55 is slightly stronger than that on the Cu(111) surface; however, a larger nanoparticle that contains 147 atoms could effectively recover the weak binding of the H atoms. We have also investigated the H atom diffusion on the 55-atom nanoparticle and found that spillover of the produced H atoms could be a feasible process due to the low diffusion barriers. Our results have demonstrated that facile H2 dissociation and weak H atom adsorption could be combined at the nanoscale. Moreover, the effects of doping one more Pd atom on the H2 dissociation and H atom adsorption have also been investigated. We have found that both the doping Pd atoms in the most stable configuration could independently exhibit their catalytic activity, behaving as two single-atom-alloy catalysts.

  6. Wet hydrogen peroxide catalytic oxidation of phenol with FeAC (iron-embedded activated carbon) catalysts.

    Science.gov (United States)

    Liou, Rey-May; Chen, Shih-Hsiung; Huang, Cheng-Hsien; Hung, Mu-Ya; Chang, Jing-Song; Lai, Cheng-Lee

    2010-01-01

    This investigation aims at exploring the catalytic oxidation activity of iron-embedded activated carbon (FeAC) and the application for the degradation of phenol in the wet hydrogen peroxide catalytic oxidation (WHPCO). FeAC catalysts were prepared by pre-impregnating iron in coconut shell with various iron loadings in the range of 27.5 to 46.5% before they were activated. The FeAC catalysts were characterised by measuring their surface area, pore distribution, functional groups on the surface, and X-ray diffraction patterns. The effects of iron loading strongly inhibited the pore development of the catalyst but benefited the oxidation activity in WHPCO. It was found that the complete conversion of phenol was observed with all FeAC catalysts in oxidation. High level of chemical oxygen demand (COD) abatement can be achieved within the first 30 minutes of oxidation. The iron embedded in the activated carbon showed good performance in the degradation and mineralisation of phenol during the oxidation due to the active sites as iron oxides formed on the surface of the activated carbon. It was found that the embedding irons were presented in gamma-Fe(2)O(3), alpha-Fe(2)O(3), and alpha-FeCOOH forms on the activated carbon. The aging tests on FeAC catalysts showed less activity loss, and less iron leaching was found after four oxidation runs.

  7. Modeling and Simulation of the Hydrogenation of α-Methylstyrene on Catalytically Active Metal Foams as Tubular Reactor Packing

    Directory of Open Access Journals (Sweden)

    Farzad Lali

    2016-01-01

    Full Text Available This work presents a one-dimensional reactor model for a tubular reactor packed with a catalytically active foam packing with a pore density of 30 PPI in cocurrent upward flow in the example of hydrogenation reaction of α-methylstyrene to cumene. This model includes material, enthalpy, and momentum balances as well as continuity equations. The model was solved within the parameter space applied for experimental studies under assumption of a bubbly flow. The method of orthogonal collocation on finite elements was applied. For isothermal and polytropic processes and steady state conditions, axial profiles for concentration, temperature, fluid velocities, pressure, and liquid holdup were computed and the conversions for various gas and liquid flow rates were validated with experimental results. The obtained results were also compared in terms of space time yield and catalytic activity with experimental results and stirred tank and also with random packed bed reactor. The comparison shows that the application of solid foams as reactor packing is advantageous compared to the monolithic honeycombs and random packed beds.

  8. Improvement of hydrogen isotope exchange reactions on Li4SiO4 ceramic pebble by catalytic metals

    Institute of Scientific and Technical Information of China (English)

    Cheng Jian Xiao; Chun Mei Kang; Xiao Jun Chen; Xiao Ling Gao; Yang Ming Luo; Sheng Hu; Xiao Lin Wang

    2012-01-01

    Li4SiO4 ceramic pebble is considered as a candidate tritium breeding material of Chinese Helium Cooled Solid Breeder Test Blanket Module (CH HCSB TBM) for the International Thermonuclear Experimental Reactor (ITER).In this paper,Li4SiO4 ceramic pebbles deposited with catalytic metals,including Pt,Pd,Ru and Ir,were prepared by wet impregnation method.The metal particles on Li4SiO4 pebble exhibit a good promotion of hydrogen isotope exchange reactions in H2-DzO gas system,with conversion equilibrium temperature reduction of 200-300 ℃.The out-of-pile tritium release experiments were performed using 1.0 wt% Pt/Li4SiO4 and Li4SiO4 pebbles irradiated in a thermal neutron reactor.The thermal desorption spectroscopy shows that Pt was effective to increase the tritium release rate at lower temperatures,and the ratio of tritium molecule (HT) to tritiated water (HTO) of 1.0 wt% Pt/Li4SiO4 was much more than that of Li4SiO4,which released mainly as HTO.Thus,catalytic metals deposited on Li4SiO4 pebble may help to accelerate the recovery of bred tritium particularly in low temperature region,and increase the tritium molecule form released from the tritium breeding materials.

  9. Enhancement of anaerobic hydrogen production by iron and nickel

    Energy Technology Data Exchange (ETDEWEB)

    Karadag, Dogan; Puhakka, Jaakko A. [Department of Chemistry and Bioengineering, Tampere University of Technology, Tampere (Finland)

    2010-08-15

    The effects of iron and nickel on hydrogen (H{sub 2}) production were investigated in a glucose-fed anaerobic Continuous Flow Stirred Tank Reactor (ACSTR). Both iron and nickel improved the reactor performance and H{sub 2} production was enhanced by 71% with the sole iron or nickel supplementation. In all cases, H{sub 2} production yield was increased by lowering both ethanol and total metabolites production and increasing butyrate production. Furthermore, iron and nickel slightly increased biomass production while glucose degradation decreased with the supplementation of nickel. Dynamic changes in bacterial composition as analyzed by 16S rRNA gene-targeted denaturing gradient gel electrophoresis (DGGE) revealed that hydrogen was produced mainly by Clostridium butyricum strains and that nickel addition decreased the microbial diversity. (author)

  10. Enhanced-hydrogen gas production through underground gasification of lignite

    Institute of Scientific and Technical Information of China (English)

    LIU Shu-qin; WANG Yuan-yuan; ZHAO Ke; YANG Ning

    2009-01-01

    Underground coal gasification is one of the clean technologies of in-situ coal utilization. Hydrogen production from underground gasification of lignite was investigated in this study based on simulation experiments. Pyrolysis of lignite, gasification activity, oxygen-steam gasification and the effect of groundwater influx were studied. As well, the advantages of lignite for stable underground gasification were analyzed. The results indicate that lignite has a high activity for gasification. Coal pyrolysis is an important source of hydrogen emission. Under special heating conditions, hydrogen is released from coal seams at temperatures above 350 ℃ and reaches its maximum value between 725 and 825 ℃. Gas with a hydrogen concentration of 40% to 50% can be continuously obtained by oxygen-steam injection at an optimum ratio of steam to oxygen, while lignite properties will ensure stable gasification. Groundwater influx can be utilized for hydrogen preparation under certain geological conditions through pressure control. Therefore, enhanced-hydrogen gas production through underground gasification of lignite has experimentally been proved.

  11. Molybdatophosphoric acid as an efficient catalyst for the catalytic and chemoselective oxidation of sulfides to sulfoxides using urea hydrogen peroxide as a commercially available oxidant

    Directory of Open Access Journals (Sweden)

    ALIREZA HASANINEJAD

    2010-03-01

    Full Text Available An efficient procedure for the chemoselective oxidation of alkyl (aryl sulfides to the corresponding sulfoxides using urea hydrogen peroxide (UHP in the presence of a catalytic amount of molybdatophosphoric acid at room temperature is described. The advantages of described method are: generality, high yield and chemoselectivity, short reaction time, low cost and compliment with green chemistry protocols.

  12. Facile synthesis of polypyrrole functionalized nickel foam with catalytic activity comparable to Pt for the poly-generation of hydrogen and electricity

    Science.gov (United States)

    Tang, Tiantian; Li, Kan; Shen, Zhemin; Sun, Tonghua; Wang, Yalin; Jia, Jinping

    2016-01-01

    Polypyrrole functionalized nickel foam is facilely prepared through the potentiostatic electrodeposition. The PPy-functionalized Ni foam functions as a hydrogen-evolution cathode in a rotating disk photocatalytic fuel cell, in which hydrogen energy and electric power are generated by consuming organic wastes. The PPy-functionalized Ni foam cathode exhibits stable catalytic activities after thirteen continuous runs. Compared with net or plate structure, the Ni foam with a unique three-dimensional reticulate structure is conducive to the electrodeposition of PPy. Compared with Pt-group electrode, PPy-coated Ni foam shows a satisfactory catalytic performance for the H2 evolution. The combination of PPy and Ni forms a synergistic effect for the rapid trapping and removal of proton from solution and the catalytic reduction of proton to hydrogen. The PPy-functionalized Ni foam could be applied in photocatalytic and photoelectrochemical generation of H2. In all, we report a low cost, high efficient and earth abundant PPy-functionalized Ni foam with a satisfactory catalytic activities comparable to Pt for the practical application of poly-generation of hydrogen and electricity.

  13. Catalytic reduction of nitrate and nitrite ions by hydrogen : investigation of the reaction mechanism over Pd and Pd-Cu catalysts

    NARCIS (Netherlands)

    Ilinitch, OM; Nosova, LV; Gorodetskii, VV; Ivanov, VP; Trukhan, SN; Gribov, EN; Bogdanov, SV; Cuperus, FP

    2000-01-01

    The catalytic behavior of mono- and bimetallic catalysts with Pd and/or Cu supported over gamma-Al2O3 in the reduction of aqueous nitrate and nitrite ions by hydrogen was investigated. The composition of the supported metal catalysts was analysed using secondary ion mass spectroscopy (SIMS) and X-ra

  14. Catalytic enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxybenzaldehyde using cyclo-His-(αMe)Phe as catalyst

    NARCIS (Netherlands)

    Hulst, Ron; Broxterman, Quirinus B.; Kamphuis, Johan; Formaggio, Fernando; Crisma, Marco; Toniolo, Claudio; Kellogg, Richard M.

    1997-01-01

    Two cyclo-dipeptides based on His and the unnatural (αMe)Phe have been examined as catalysts in the enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxy-benzaldehyde. The synthesis, catalytic activity and NMR study towards the mechanism of this reaction are presented.

  15. Catalytic enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxybenzaldehyde using cyclo-His-(alpha-Me)Phe as catalyst

    NARCIS (Netherlands)

    Hulst, R; Broxterman, QB; Kamphuis, J; Formaggio, F; Crisma, M; Toniolo, C; Kellogg, RM

    1997-01-01

    Two cyclo-dipeptides based on His and the unnatural (alpha Me)Phe have been examined as catalysts in the enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxy-benzaldehyde. The synthesis, catalytic activity and NMR study towards the mechanism of this reaction are presented. (C)

  16. Production of hydrogen in a conventional microwave oven

    Science.gov (United States)

    Nomura, Shinfuku; Toyota, Hiromichi; Mukasa, Shinobu; Yamashita, Hiroshi; Maehara, Tsunehiro; Kawashima, Ayato

    2009-10-01

    Hydrogen is produced by generating in-liquid plasma in a conventional microwave oven. A receiving antenna unit consisting of seven copper rods is placed at the bottom of the reactor furnace in the microwave oven. 2.45 GHz microwave in-liquid plasma can be generated at the tips of the electrodes in the microwave oven. When the n-dodecane is decomposed by plasma, 74% pure hydrogen gas can be achieved with this device. The hydrogen generation efficiency for a 750 W magnetron output is estimated to be approximately 56% of that of the electrolysis of water. Also, in this process up to 4 mg/s of solid carbon can be produced at the same time. The present process enables simultaneous production of hydrogen gas and the carbide in the hydrocarbon liquid.

  17. Studies on membrane acid electrolysis for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Marco Antonio Oliveira da; Linardi, Marcelo; Saliba-Silva, Adonis Marcelo [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Celulas a Combustivel e Hidrogenio], Email: saliba@ipen.br

    2010-07-01

    Hydrogen represents great opportunity to be a substitute for fossil fuels in the future. Water as a renewable source of hydrogen is of great interest, since it is abundant and can decompose, producing only pure H{sub 2} and O{sub 2}. This decomposition of water can be accomplished by processes such as electrolysis, thermal decomposition and thermochemical cycles. The electrolysis by membrane has been proposed as a viable process for hydrogen production using thermal and electrical energy derived from nuclear energy or any renewable source like solar energy. In this work, within the context of optimization of the electrolysis process, it is intended to develop a mathematical model that can simulate and assist in parameterization of the electrolysis performed by polymer membrane electrolytic cell. The experimental process to produce hydrogen via the cell membrane, aims to optimize the amount of gas produced using renewable energy with noncarbogenic causing no harm by producing gases deleterious to the environment. (author)

  18. Hydrogen production by ethanol steam reforming over Cu-Ni supported catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Vizcaino, A.J.; Carrero, A.; Calles, J.A. [Department of Chemical and Environmental Technology, Rey Juan Carlos University, Escuela Superior de Ciencias Experimentales y Tecnologia (ESCET), c/ Tulipan s/n, 28933 Mostoles (Spain)

    2007-07-15

    In the present work, Cu-Ni supported catalysts were tested in ethanol steam reforming reaction. Two commercial amorphous solids (SiO{sub 2} and {gamma}-Al{sub 2}O{sub 3}) and three synthesized materials (MCM-41, SBA-15 and ZSM-5 nanocrystalline) were used as support. A series of Cu-Ni/SiO{sub 2} catalysts with different Cu and Ni content were also prepared. It was found that aluminium containing supports favour ethanol dehydration to ethylene in the acid sites, which in turn, promotes the coke deactivation process. The highest hydrogen selectivity is achieved with the Cu-Ni/SBA-15 catalyst, due to a smaller metallic crystallite size. Nevertheless, the Cu-Ni/SiO{sub 2} catalyst showed the best catalytic performance, since a better equilibrium between high hydrogen selectivity and CO{sub 2}/CO{sub x} ratio is obtained. It was seen that nickel is the phase responsible for hydrogen production in a greater grade, although both CO production and coke deposition are decreased when copper is added to the catalyst. (author)

  19. Hydrogen production from high-moisture content biomass in supercritical water

    Energy Technology Data Exchange (ETDEWEB)

    Antal, M.J. Jr.; Adschiri, T.; Ekbom, T. [Univ. of Hawaii, Honolulu, HI (United States)] [and others

    1996-10-01

    Most hydrogen is produced by steam reforming methane at elevated pressures. The goal of this research is to develop commercial processes for the catalytic steam reforming of biomass and other organic wastes at high pressures. This approach avoids the high cost of gas compression and takes advantage of the unique properties of water at high pressures. Prior to this year the authors reported the ability of carbon to catalyze the decomposition of biomass and related model compounds in supercritical water. The product gas consists of hydrogen, carbon dioxide, carbon monoxide, methane, and traces of higher hydrocarbons. During the past year the authors have: (a) developed a method to extend the catalyst life, (b) begun studies of the role of the shift reaction, (c) completed studies of carbon dioxide absorption from the product effluent by high pressure water, (d) measured the rate of carbon catalyst gasification in supercritical water, (e) discovered the pumpability of oil-biomass slurries, and (f) completed the design and begun fabrication of a flow reactor that will steam reform whole biomass feedstocks (i.e. sewage sludge) and produce a hydrogen rich synthesis gas at very high pressure (>22 MPa).

  20. Catalytic Ring Hydrogenation of Benzoic Acid with Supported Transition Metal Catalysts in scCO2

    Directory of Open Access Journals (Sweden)

    Fengyu Zhao

    2007-07-01

    Full Text Available The ring hydrogenation of benzoic acid to cyclohexanecarboxylic acid overcharcoal-supported transition metal catalysts in supercritical CO2 medium has been studiedin the present work. The cyclohexanecarboxylic acid can be produced efficiently insupercritical CO2 at the low reaction temperature of 323 K. The presence of CO2 increasesthe reaction rate and several parameters have been discussed.

  1. Catalytic Ring Hydrogenation of Benzoic Acid with Supported Transition Metal Catalysts in scCO2

    OpenAIRE

    2007-01-01

    The ring hydrogenation of benzoic acid to cyclohexanecarboxylic acid over charcoal-supported transition metal catalysts in supercritical CO2 medium has been studied in the present work. The cyclohexanecarboxylic acid can be produced efficiently in supercritical CO2 at the low reaction temperature of 323 K. The presence of CO2 increases the reaction rate and several parameters have been discussed.

  2. Catalytic activity of in situ synthesized MoWNi sulfides in hydrogenation of aromatic hydrocarbons

    Science.gov (United States)

    Topolyuk, Yu. A.; Maksimov, A. L.; Kolyagin, Yu. G.

    2017-02-01

    MoWNi-sulfide catalysts were obtained in situ by thermal decomposition of metal-polymer precursors based on the copolymers of polymaleic anhydride in a hydrocarbon raw material. The activity of the synthesized catalysts in hydrogenation of bicyclic aromatic hydrocarbons was studied, and the composition and structure of active phase nanoparticles were determined.

  3. The remarkable effect of oxygen on the N2 selectivity of water catalytic denitrification by hydrogen.

    Science.gov (United States)

    Constantinou, Costas L; Costa, Costas N; Efstathiou, Angelos M

    2007-02-01

    The selective catalytic reduction of nitrates (NO3-) in pure water toward N2 formation by the use of gaseous H2 and in the presence of O2 (air) at 1 atm total pressure and 25 degrees C has been investigated over Pd-Cu supported on various mixed metal oxides, x wt % MO(x(/gamma-Al2O3 (MO(x) = CeO2, SrO, Mn2O3, Cr2O3, Y2O3, and TiO2). It is demonstrated for the firsttime that a remarkable improvement in N2 reaction selectivity (by 80 percentage units) can be achieved when oxygen is present in the reducing feed gas stream. In particular, significantly lower reaction selectivities toward NH4+ and NO2- can be obtained, whereas the rate of NO3- conversion is not significantly affected. Moreover, it was shown thatthe same effect is obtained over the Pd-Cu-supported catalysts irrespective to the chemical composition of support and the initial concentration of nitrates in water used. The Pd-Cu clusters supported on 4.8 wt%TiO2/gamma-Al2O3 resulted in a solid with the best catalytic behavior compared with the rest of supports examined, both in the presence and in the absence of oxygen in the reducing feed gas stream. DRIFTS studies performed following catalytic reduction by H2 of NO3- in water revealed that the presence of TiO2 in the Pd-Cu/TiO2-Al2O3 system enhanced the reactivity of adsorbed bidentate nitrate species toward H2. Nitrosyl species adsorbed on the alumina and titania support surfaces are considered as active intermediate species of the selective catalytic reduction of NO3- by H2 in water. Pd-Cu/TiO2-Al2O3 appears to be the most selective catalyst ever reported in the literature for the reduction of nitrates present in pure water into N2 by a reducing gas mixture of H2/air.

  4. Production of bio-fuels from cottonseed cake by catalytic pyrolysis under steam atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Puetuen, Ersan [Department of Material Science and Engineering, Anadolu University, Iki Eyluel Campus, 26555 Eskisehir (Turkey); Uzun, Basak Burcu; Puetuen, Ayse Eren [Department of Chemical Engineering, Anadolu University, Iki Eyluel Campus, 26555 Eskisehir (Turkey)

    2006-06-15

    The purpose of this study is to evaluate the amounts of catalytic pyrolysis products of cottonseed cake in steam atmosphere and investigate the effects of both zeolite and steam on pyrolysis yields. The effect of steam was investigated by co-feeding steam at various velocities (0.6:1.3:2.7cms{sup -1}) in the presence of zeolite (20wt% of feed). Liquid pyrolysis products obtained at the most appropriate conditions were fractionated by column chromatography. Elemental analysis and FT-IR were applied on both of these liquid products and their sub-fractions. The H/C ratios obtained from elemental analysis were compared with the petroleum products. The aliphatic sub-fractions of the oils were then analysed by capillary column gas chromatography. Further structural analysis of pyrolysis oil was conducted using {sup 1}H-NMR spectroscopy. The characterization has shown that the bio-oil obtained from catalytic and steam pyrolysis of cottonseed cake was more beneficial than those obtained from non-catalytic and catalytic works under static and nitrogen atmospheres. (author)

  5. Catalytic C-C Bond Cleavage for the Production of Chemicals from Lignin

    NARCIS (Netherlands)

    Jastrzebski, R.

    2016-01-01

    Lignin is a major component of lignocellulosic biomass and could be an important renewable feedstock in industry for the production of (aromatic) bulk and fine chemicals. To this end, the development of new catalytic processes is required; both to depolymerise the biopolymer into small aromatic buil

  6. Experimental and Computational Mechanistic Studies Guiding the Rational Design of Molecular Electrocatalysts for Production and Oxidation of Hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Raugei, Simone; Helm, Monte L.; Hammes-Schiffer, Sharon; Appel, Aaron M.; O' Hagan, Molly J.; Wiedner, Eric S.; Bullock, R. Morris

    2016-01-19

    Understanding how to control the movement of protons and electrons is crucial to the design of fast, efficient electrocatalysts for hydrogen production and oxidation based on earth-abundant metals. Our work seeks to elucidate fundamental questions about proton movement. We have demonstrated that incorporating a pendant amine functioning as a proton relay in the second coordination sphere of a metal complex helps proton mobility, resulting in faster and more energy efficient catalysts. Proton transfer reactions are often rate limiting, and are influenced by several factors, such as pKa values, steric effects, hydrogen bonding, and solvation/desolvation of the exogenous base and acid employed. The presence of multiple protonation sites introduces branching points along the catalytic cycle, making less productive pathways accessible, or leading to the formation of stable off-cycle species. Using ligands with only one pendant amine mitigates this problem and results in catalysts with high rates for production of H2. For H2 oxidation catalysts, iron complexes with a high H2 binding affinity were developed. However, the improvement of H2 binding enthalpy resulted in a pKa mismatch between the protonated metal center and the protonated pendant amine, and consequently to rate-limiting intramolecular proton movement. Taken altogether, our results demonstrate the necessity of optimizing the entire catalytic cycle, as the optimization of a specific catalytic step can negatively influence another step, and not necessarily lead to better catalytic performance. We discuss a general procedure, based on thermodynamic arguments, which allows the simultaneous minimization of the free energy change of each catalytic step, yielding a nearly flat free energy surface, with no large barriers due to energy mismatches from either high- or low-energy intermediates. This research was supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by

  7. Human Cystathionine-β-Synthase Phosphorylation on Serine227 Modulates Hydrogen Sulfide Production in Human Urothelium.

    Directory of Open Access Journals (Sweden)

    Roberta d'Emmanuele di Villa Bianca

    Full Text Available Urothelium, the epithelial lining the inner surface of human bladder, plays a key role in bladder physiology and pathology. It responds to chemical, mechanical and thermal stimuli by releasing several factors and mediators. Recently it has been shown that hydrogen sulfide contributes to human bladder homeostasis. Hydrogen sulfide is mainly produced in human bladder by the action of cystathionine-β-synthase. Here, we demonstrate that human cystathionine-β-synthase activity is regulated in a cGMP/PKG-dependent manner through phosphorylation at serine 227. Incubation of human urothelium or T24 cell line with 8-Bromo-cyclic-guanosine monophosphate (8-Br-cGMP but not dibutyryl-cyclic-adenosine monophosphate (d-cAMP causes an increase in hydrogen sulfide production. This result is congruous with the finding that PKG is robustly expressed but PKA only weakly present in human urothelium as well as in T24 cells. The cGMP/PKG-dependent phosphorylation elicited by 8-Br-cGMP is selectively reverted by KT5823, a specific PKG inhibitor. Moreover, the silencing of cystathionine-β-synthase in T24 cells leads to a marked decrease in hydrogen sulfide production either in basal condition or following 8-Br-cGMP challenge. In order to identify the phosphorylation site, recombinant mutant proteins of cystathionine-β-synthase in which Ser32, Ser227 or Ser525 was mutated in Ala were generated. The Ser227Ala mutant cystathionine-β-synthase shows a notable reduction in basal biosynthesis of hydrogen sulfide becoming unresponsive to the 8-Br-cGMP challenge. A specific antibody that recognizes the phosphorylated form of cystathionine-β-synthase has been produced and validated by using T24 cells and human urothelium. In conclusion, human cystathionine-β-synthase can be phosphorylated in a PKG-dependent manner at Ser227 leading to an increased catalytic activity.

  8. Photosynthetic Hydrogen and Oxygen Production by Green Algae

    Energy Technology Data Exchange (ETDEWEB)

    Greenbaum, E.; Lee, J.W.

    1999-08-22

    Photosynthesis research at Oak Ridge National Laboratory is focused on hydrogen and oxygen production by green algae in the context of its potential as a renewable fuel and chemical feed stock. Beginning with its discovery by Gaffron and Rubin in 1942, motivated by curiosity-driven laboratory research, studies were initiated in the early 1970s that focused on photosynthetic hydrogen production from an applied perspective. From a scientific and technical point of view, current research is focused on optimizing net thermodynamic conversion efficiencies represented by the Gibbs Free Energy of molecular hydrogen. The key research questions of maximizing hydrogen and oxygen production by light-activated water splitting in green algae are: (1) removing the oxygen sensitivity of algal hydrogenases; (2) linearizing the light saturation curves of hotosynthesis throughout the entire range of terrestrial solar irradiance-including the role of bicarbonate and carbon dioxide in optimization of photosynthetic electron transpor;t and (3) constructing real-world bioreactors, including the generation of hydrogen and oxygen against workable back pressures of the photoproduced gases.

  9. Designer proton-channel transgenic algae for photobiological hydrogen production

    Science.gov (United States)

    Lee, James Weifu

    2011-04-26

    A designer proton-channel transgenic alga for photobiological hydrogen production that is specifically designed for production of molecular hydrogen (H.sub.2) through photosynthetic water splitting. The designer transgenic alga includes proton-conductive channels that are expressed to produce such uncoupler proteins in an amount sufficient to increase the algal H.sub.2 productivity. In one embodiment the designer proton-channel transgene is a nucleic acid construct (300) including a PCR forward primer (302), an externally inducible promoter (304), a transit targeting sequence (306), a designer proton-channel encoding sequence (308), a transcription and translation terminator (310), and a PCR reverse primer (312). In various embodiments, the designer proton-channel transgenic algae are used with a gas-separation system (500) and a gas-products-separation and utilization system (600) for photobiological H.sub.2 production.

  10. Sub-10 nm Platinum Nanocrystals with Size and Shape Control: Catalytic Study for Ethylene and Pyrrole Hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Tsung, Chia-Kuang; Kuhn, John N.; Huang, Wenyu; Aliaga, Cesar; Hung, Ling-I; Somorjai, Gabor A.; Yang, Peidong

    2009-03-02

    Platinum nanocubes and nanopolyhedra with tunable size from 5 to 9 nm were synthesized by controlling the reducing rate of metal precursor ions in a one-pot polyol synthesis. A two-stage process is proposed for the simultaneous control of size and shape. In the first stage, the oxidation state of the metal ion precursors determined the nucleation rate and consequently the number of nuclei. The reaction temperature controlled the shape in the second stage by regulation of the growth kinetics. These well-defined nanocrystals were loaded into MCF-17 mesoporous silica for examination of catalytic properties. Pt loadings and dispersions of the supported catalysts were determined by elemental analysis (ICP-MS) and H2 chemisorption isotherms, respectively. Ethylene hydrogenation rates over the Pt nanocrystals were independent of both size and shape and comparable to Pt single crystals. For pyrrole hydrogenation, the nanocubes enhanced ring-opening ability and thus showed a higher selectivity to n-butylamine as compared to nanopolyhedra.

  11. Experimental studies on catalytic hydrogen recombiners for light water reactors; Experimentelle Untersuchungen zu katalytischen Wasserstoffkombinatoren fuer Leichtwasserreaktoren

    Energy Technology Data Exchange (ETDEWEB)

    Drinovac, P.

    2006-06-19

    In the course of core melt accidents in nuclear power plants a large amount of hydrogen can be produced and form an explosive or even detonative gas mixture with aerial oxygen in the reactor building. In the containment atmosphere of pressurized water reactors hydrogen combines a phlogistically with the oxygen present to form water vapor even at room temperature. In the past, experimental work conducted at various facilities has contributed little or nothing to an understanding of the operating principles of catalytic recombiners. Hence, the purpose of the present study was to conduct detailed investigations on a section of a recombiner essentially in order to deepen the understanding of reaction kinetics and heat transport processes. The results of the experiments presented in this dissertation form a large data base of measurements which provides an insight into the processes taking place in recombiners. The reaction-kinetic interpretation of the measured data confirms and deepens the diffusion theory - proposed in an earlier study. Thus it is now possible to validate detailed numeric models representing the processes in recombiners. Consequently the present study serves to broaden and corroborate competence in this significant area of reactor technology. In addition, the empirical knowledge thus gained may be used for a critical reassessment of previous numeric model calculations. (orig.)

  12. Catalytic conversion of biomass-derived feedstocks into olefins and aromatics with ZSM-5: the hydrogen to carbon effective ratio

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Huiyan; Cheng, Yu-Ting; Vispute, Tushar; Xiao, R; Huber, George W.

    2011-01-01

    Catalytic conversion of ten biomass-derived feedstocks, i.e.glucose, sorbitol, glycerol, tetrahydrofuran, methanol and different hydrogenated bio-oil fractions, with different hydrogen to carbon effective (H/C{sub eff}) ratios was conducted in a gas-phase flow fixed-bed reactor with a ZSM-5 catalyst. The aromatic + olefin yield increases and the coke yield decreases with increasing H/C{sub eff} ratio of the feed. There is an inflection point at a H/C{sub eff} ratio = 1.2, where the aromatic + olefin yield does not increase as rapidly as it does prior to this point. The ratio of olefins to aromatics also increases with increasing H/C{sub eff} ratio. CO and CO₂ yields go through a maximum with increasing H/C{sub eff} ratio. The deactivation rate of the catalyst decreases significantly with increasing H/C{sub eff} ratio. Coke was formed from both homogeneous and heterogeneous reactions. Thermogravimetric analysis (TGA) for the ten feedstocks showed that the formation of coke from homogeneous reactions decreases with increasing H/C{sub eff} ratio. Feedstocks with a H/C{sub eff} ratio less than 0.15 produce large amounts of undesired coke (more than 12 wt%) from homogeneous decomposition reactions. This paper shows that the conversion of biomass-derived feedstocks into aromatics and olefins using zeolite catalysts can be explained by the H/C{sub eff} ratio of the feed.

  13. Dendrimer Templated Synthesis of One Nanometer Rh and Pt Particles Supported on Mesoporous Silica: Catalytic Activity for Ethylene and Pyrrole Hydrogenation.

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Wenyu; Kuhn, John N.; Tsung, Chia-Kuang; Zhang, Yawen; Habas, Susan E.; Yang, Peidong; Somorjai, Gabor A.

    2008-05-09

    Monodisperse rhodium (Rh) and platinum (Pt) nanoparticles as small as {approx}1 nm were synthesized within a fourth generation polyaminoamide (PAMAM) dendrimer, a hyperbranched polymer, in aqueous solution and immobilized by depositing onto a high-surface-area SBA-15 mesoporous support. X-ray photoelectron spectroscopy indicated that the as-synthesized Rh and Pt nanoparticles were mostly oxidized. Catalytic activity of the SBA-15 supported Rh and Pt nanoparticles was studied with ethylene hydrogenation at 273 and 293 K in 10 torr of ethylene and 100 torr of H{sub 2} after reduction (76 torr of H{sub 2} mixed with 690 torr of He) at different temperatures. Catalysts were active without removing the dendrimer capping but reached their highest activity after hydrogen reduction at a moderate temperature (423 K). When treated at a higher temperature (473, 573, and 673 K) in hydrogen, catalytic activity decreased. By using the same treatment that led to maximum ethylene hydrogenation activity, catalytic activity was also evaluated for pyrrole hydrogenation.

  14. CERAMIC MEMBRANES FOR HYDROGEN PRODUCTION FROM COAL

    Energy Technology Data Exchange (ETDEWEB)

    George R. Gavalas

    2004-04-01

    The preparation and performance of membranes for application to hydrogen separation from coal-derived gas is described. The membrane material investigated was dense amorphous silica deposited on a suitable support by chemical vapor deposition (CVD). Two types of support materials were pursued. One type consisted of a two-layer composite, zeolite silicalite/{alpha}-Al{sub 2}O{sub 3}, in the form of tubes approximately 0.7 cm in diameter. The other type was porous glass tubes of diameter below 0.2 cm. The first type of support was prepared starting from {alpha}-Al{sub 2}O{sub 3} tubes of 1{micro}m mean pore diameter and growing by hydrothermal reaction a zeolite silicalite layer inside the pores of the alumina at the OD side. After calcination to remove the organic template used in the hydrothermal reaction, CVD was carried out to deposit the final silica layer. CVD was carried out by alternating exposure of the surface with silicon tetrachloride and water vapor. SEM and N2 adsorption measurements were employed to characterize the membranes at several stages during their preparation. Permeation measurements of several gases yielded H{sub 2}:N{sub 2} ideal selectivity of 150-200 at room temperature declining to 110 at 250 C. The second type of support pursued was porous glass tubes prepared by a novel extrusion technique. A thick suspension of borosilicate glass powder in a polyethersulfone solution was extruded through a spinneret and after gelation the glass-polymer tube was heat treated to obtain a gas-tight glass tube. Leaching of the glass tube in hot water yielded connected pores with diameter on the order of 100 nm. CVD of the final silica layer was not carried out on these tubes on account of their large pore size.

  15. Experimental study of hydrogen production by direct decomposition of water

    Science.gov (United States)

    Bilgen, E.; Galindo, J.; Baykara, S. Z.

    The hydrogen production by direct decomposition of water in a solar furnace is studied. The set-up is a horizontal axis system consisting of two 1.0 kW parabolic concentrators, both powered by a single heliostat. A temperature of 3000 K is possible. The water is fed to the reactor installed at the focal space of the concentrator, and the steam is decomposed at about 2500 K. The reactor consisted of a cylindrical cavity type refractory receiver covered with a silica cupola. The steam was introduced at a known rate into the cavity and the product gases were quenched. After the condensation of steam, hydrogen and oxygen were collected in a reservoir. Results indicate that with an optimized system, it is possible to produce hydrogen at about 70 percent rate of the theoretical value at the temperature level studied.

  16. A Study of a nuclear hydrogen production demonstration plant

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Jong Hwa and others [KAERI, Daejeon (Korea, Republic of); Bae, Ki Kwang [Korea Institute of Energy Research, Daejeon (Korea, Republic of); Jung, Kwang Deog [Korea Institute od Science and Technology, Seoul (Korea, Republic of)

    2007-03-15

    The current energy supply system is burdened environmental and supply problems. The concept of a hydrogen economy has been actively discussed worldwide. KAERI has set up a plan to demonstrate massive production of hydrogen using a VHTR by the early 2020s. The technological gap to meet this goal was identified during the past few years. The hydrogen production process, a process heat exchanger, the efficiency of an I/S thermochemical cycle, the manufacturing of components, the analysis tools of VHTR, and a coated particle fuel are key areas that require urgent development. Candidate NHDD plant designs based on a 200 MWth VHTR core and I/S thermochemical process have been studied and some of analysis results are presented in this paper.

  17. Nuclear driven water decomposition plant for hydrogen production

    Science.gov (United States)

    Parker, G. H.; Brecher, L. E.; Farbman, G. H.

    1976-01-01

    The conceptual design of a hydrogen production plant using a very-high-temperature nuclear reactor (VHTR) to energize a hybrid electrolytic-thermochemical system for water decomposition has been prepared. A graphite-moderated helium-cooled VHTR is used to produce 1850 F gas for electric power generation and 1600 F process heat for the water-decomposition process which uses sulfur compounds and promises performance superior to normal water electrolysis or other published thermochemical processes. The combined cycle operates at an overall thermal efficiency in excess of 45%, and the overall economics of hydrogen production by this plant have been evaluated predicated on a consistent set of economic ground rules. The conceptual design and evaluation efforts have indicated that development of this type of nuclear-driven water-decomposition plant will permit large-scale economic generation of hydrogen in the 1990s.

  18. Methane and hydrogen production from crop biomass through anaerobic digestion

    Energy Technology Data Exchange (ETDEWEB)

    Pakarinen, O.

    2011-07-01

    The feasibility of methane and hydrogen production from energy crops through anaerobic digestion was evaluated in this thesis. The effects of environmental conditions, e.g. pH and temperature, as well as inoculum source on H{sub 2} yield were studied in batch assays. In addition, the effects of pre-treatments on methane and hydrogen yield as well as the feasibility of two-stage H{sub 2} + CH{sub 4} production was evaluated. Moreover, the effect of storage on methane yield of grasses was evaluated. Monodigestion of grass silage for methane production was studied, as well as shifting the methanogenic process to hydrogenic. Hydrogen production from grass silage and maize was shown to be possible with heat-treated inoculum in batch assays, with highest H{sub 2} yields of 16.0 and 9.9 ml gVS{sub added}-1 from untreated grass silage and maize, respectively. Pre-treatments (NaOH, HCl and water-extraction) showed some potential in increasing H{sub 2} yields, while methane yields were not affected. Two-stage H{sub 2} + CH{sub 4} producing process was shown to improve CH{sub 4} yields when compared to traditional one-stage CH{sub 4} process. Methane yield from grass silage monodigestion in continuously stirred tank reactor (CSTR) with organic loading rate (OLR) of 2 kgVS (m3d)-1 and hydraulic retention time (HRT) of 30 days was at most 218 l kgVS{sub fed}-1. Methanogenic process was shifted to hydrogenic by increasing the OLR to 10 kgVS (m3d)-1 and shortening the HRT to 6 days. Highest H{sub 2} yield from grass silage was 42 l kgVS{sub fed}-1 with a maximum H{sub 2} content of 24 %. Energy crops can be successfully stored even for prolonged periods without decrease in methane yield. However, under sub-optimal storage conditions loss in volatile solids (VS) content and methane yield can occur. According to present results energy crops such as grass silage and maize can be converted to hydrogen or methane in AD process. Hydrogen energy yields are typically only 2-5 % of the

  19. Catalytic Conversion of Lignin for the Production of Aromatics

    NARCIS (Netherlands)

    Jongerius, A.L.

    2013-01-01

    With the depletion of fossil fuels and increasing environmental awareness, there is much interest in the use of biomass as a more sustainable alternative feedstock for the production of renewable fuels and chemicals. Non-edible lignocellulosic biomass is the major and most sustainable source of biom

  20. Sorption enhanced reaction process (SERP) for production of hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Sircar, S.; Anand, M.; Carvill, B. [Air Products and Chemicals, Inc., Allentown, PA (United States)] [and others

    1995-09-01

    Sorption Enhanced Reaction (SER) is a novel process that is being developed for the production of lower cost hydrogen by steam-methane reforming (SMR). In this process, the reaction of methane with steam is carried out in the presence of an admixture of a catalyst and a selective adsorbent for carbon dioxide. The consequences of SER are: (1) reformation reaction at a significantly lower temperature (300-500{degrees}C) than conventional SMR (800-1100{degrees}C), while achieving the same conversion of methane to hydrogen, (2) the product hydrogen is obtained at reactor pressure (200-400 psig) and at 99+% purity directly from the reactor (compared to only 70-75% H{sub 2} from conventional SMR reactor), (3) downstream hydrogen purification step is either eliminated or significantly reduced in size. The early focus of the program will be on the identification of an adsorbent/chemisorbent for CO{sub 2} and on the demonstration of the SER concept for SMR in our state-of-the-art bench scale process. In the latter stages, a pilot plant will be built to scale-up the technology and to develop engineering data. The program has just been initiated and no significant results for SMR will be reported. However, results demonstrating the basic principles and process schemes of SER technology will be presented for reverse water gas shift reaction as the model reaction. If successful, this technology will be commercialized by Air Products and Chemicals, Inc. (APCI) and used in its existing hydrogen business. APCI is the world leader in merchant hydrogen production for a wide range of industrial applications.

  1. Surface features and catalytic performance of platinum/alumina catalysts in slurry-phase hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Gutierrez-Ortiz, M.A.; Gonzalez-Marcos, M.P.; Arnaiz-Aguilar, S.; Gonzalez-Marcos, J.A.; Gonzalez-Velasco, J.R. (Univ. del Pais Vasco/Euskal Hirrika Unibertsitatea, Bilbao (Spain). Dept. de Ingenierlla Quimica)

    1993-11-01

    Several platinum catalysts supported on three commercial [gamma]-aluminas were prepared by impregnation and anionic exchange using aqueous solutions of H[sub 2]PtCl[sub 6]. A number of methods were used to characterize the precursors as well as the final catalysts, including TGA, TPR, and hydrogen chemisorption at 298 K. TPR measurements showed two reduction peaks for the catalysts: the first one corresponding to reduction of the metal precursor to platinum and the second one associated to formation of a surface complex, Pt-Al[sub 2]O[sub 3[minus]x], With partial reduction of the support. The activity of the different catalysts was tested in the slurry-phase hydrogenation of benzene. The results obtained in the activity measurements have been correlated to the characteristics of the catalysts.

  2. High Intrinsic Catalytic Activity of Two-Dimensional Boron Monolayers for Hydrogen Evolution Reaction

    CERN Document Server

    Shi, Li; Ouyang, Yixin; Wang, Jinlan

    2016-01-01

    Two-dimensional (2D) boron monolayers have been successfully synthesized on silver substrate very recently. Their potential application is thus of great significance. In this work, we explore the possibility of boron monolayers (BMs) as electrocatalysts for hydrogen evolution reaction (HER) by first-principle method. Our calculations show that the BMs are active catalysts for HER with nearly zero free energy of hydrogen adsorption, metallic conductivity and plenty of active sites in the basal plane. The effect of the substrate on the HER activity is further assessed. It is found that the substrate has a positive effect on the HER performance caused by the competitive effect of mismatch strain and charge transfer. The indepth understanding of the structure dependent HER activity is also provided.

  3. Hydricity of an Fe-H Species and Catalytic CO2 Hydrogenation.

    Science.gov (United States)

    Fong, Henry; Peters, Jonas C

    2015-06-01

    Despite renewed interest in carbon dioxide (CO2) reduction chemistry, examples of homogeneous iron catalysts that hydrogenate CO2 are limited compared to their noble-metal counterparts. Knowledge of the thermodynamic properties of iron hydride complexes, including M-H hydricities (ΔGH(-)), could aid in the development of new iron-based catalysts. Here we present the experimentally determined hydricity of an iron hydride complex: (SiP(iPr)3)Fe(H2)(H), ΔGH(-) = 54.3 ± 0.9 kcal/mol [SiP(iPr)3 = [Si(o-C6H4PiPr2)3](-)]. We also explore the CO2 hydrogenation chemistry of a series of triphosphinoiron complexes, each with a distinct apical unit on the ligand chelate (Si(-), C(-), PhB(-), N, B). The silyliron (SiP(R)3)Fe (R = iPr and Ph) and boratoiron (PhBP(iPr)3)Fe (PhBP(iPr)3 = [PhB(CH2PiPr2)3](-)) systems, as well as the recently reported (CP(iPr)3)Fe (CP(iPr)3 = [C(o-C6H4PiPr2)3](-)), are also catalysts for CO2 hydrogenation in methanol and in the presence of triethylamine, generating methylformate and triethylammonium formate at up to 200 TON using (SiP(Ph)3)FeCl as the precatalyst. Under stoichiometric conditions, the iron hydride complexes of this series react with CO2 to give formate complexes. Finally, the proposed mechanism of the (SiP(iPr)3)-Fe system proceeds through a monohydride intermediate (SiP(iPr)3)Fe(H2)(H), in contrast to that of the known and highly active tetraphosphinoiron, (tetraphos)Fe (tetraphos = P(o-C6H4PPh2)3), CO2 hydrogenation catalyst.

  4. Hydrogen production from water hyacinth through dark- and photo- fermentation

    Energy Technology Data Exchange (ETDEWEB)

    Su, Huibo; Cheng, Jun; Zhou, Junhu; Song, Wenlu; Cen, Kefa [State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou 310027 (China)

    2010-09-15

    This article discusses the method of producing hydrogen from water hyacinth. Water hyacinth was pretreated with microwave heating and alkali to enhance the enzymatic hydrolysis and hydrogen production in a two-step process of dark- and photo- fermentation. Water hyacinth with various concentrations of 10-40 g/l was pretreated with four methods: (1) steam heating; (2) steam heating and microwave heating/alkali pretreatment; (3) steam heating and enzymatic hydrolysis; (4) steam heating, microwave heating/alkali pretreatment and enzymatic hydrolysis. Water hyacinth (20 g/l) pretreated with method 4 gave the maximum reducing sugar yield of 30.57 g/100 g TVS, which was 45.6% of the theoretical reducing sugar yield (67.0 g/100 g TVS). The pretreated water hyacinth was used to produce hydrogen by mixed H{sub 2}-producing bacteria in dark fermentation. The maximum hydrogen yield of 76.7 ml H{sub 2}/g TVS was obtained at 20 g/l of water hyacinth. The residual solutions from dark fermentation (mainly acetate and butyrate) were used to further produce hydrogen by immobilized Rhodopseudomonas palustris in photo fermentation. The maximum hydrogen yield of 522.6 ml H{sub 2}/g TVS was obtained at 10 g/l of water hyacinth. Through a combined process of dark- and photo- fermentation, the maximum hydrogen yield from water hyacinth was dramatically enhanced from 76.7 to 596.1 ml H{sub 2}/g TVS, which was 59.6% of the theoretical hydrogen yield. (author)

  5. Bio-hydrogen production from renewable organic wastes

    Energy Technology Data Exchange (ETDEWEB)

    Shihwu Sung

    2004-04-30

    Methane fermentation has been in practice over a century for the stabilization of high strength organic waste/wastewater. Although methanogenesis is a well established process and methane--the end-product of methanogenesis is a useful energy source; it is a low value end product with relatively less energy content (about 56 kJ energy/g CH{sub 4}). Besides, methane and its combustion by-product are powerful greenhouse gases, and responsible for global climate change. So there is a pressing need to explore alternative environmental technologies that not only stabilize the waste/wastewater but also generate benign high value end products. From this perspective, anaerobic bioconversion of organic wastes to hydrogen gas is an attractive option that achieves both goals. From energy security stand point, generation of hydrogen energy from renewable organic waste/wastewater could substitute non-renewable fossil fuels, over two-third of which is imported from politically unstable countries. Thus, biological hydrogen production from renewable organic waste through dark fermentation represents a critically important area of bioenergy production. This study evaluated both process engineering and microbial physiology of biohydrogen production.

  6. Hydrogen production from palm oil mill effluent by fermentation

    Energy Technology Data Exchange (ETDEWEB)

    Tanisho, S.; Shimazaki, T. [Yokohama National Univ., Shigeharu TANISHO and Tsuruyo SHIMAZAKI, Yokohama (Japan)

    2003-09-01

    Hydrogen production by fermentation was examined by using palm oil mill effluent. Clostridium butyricum produced more than 2.2 NL of hydrogen from 1 L of raw POME at pH 5.0, and Enterobacter aerogenes produced ca. 1.9 NL at pH 6.0. While from the culture liquid added 1% of peptone on the raw POME, C. butyricum produced more than 3.3 NL and also E. aerogenes 3.4 NL at pH 6.0 and 5.0, respectively. In this manner, the addition of nitrogen source to the POME liquid exerted an influence on the volume of hydrogen production. Since Aspergillus niger has ability to produce cellulase, co-cultivation of C.butyricum with A. niger was tried to utilize celluloses in the POME. Against our expectations, however, the results were lower productivities than pure cultivation's. We analyzed the components of POME by liquid chromatography and capillary electrophoresis before and after cultivation. The main substrate for hydrogen production was found to be glycerol. (authors)

  7. Non-thermal production of pure hydrogen from biomass : HYVOLUTION

    NARCIS (Netherlands)

    Claassen, P.A.M.; Vrije, de G.J.

    2006-01-01

    HYVOLUTION is the acronym of an Integrated Project ¿Non-thermal production of pure hydrogen from biomass¿ which has been granted in the Sixth EU Framework Programme on Research, Technological Development and Demonstration, Priority 6.1.ii, Sustainable Energy Systems. The aim of HYVOLUTION: ¿Developm

  8. Existing large steam power plant upgraded for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Galanti, L.; Franzoni, A.; Traverso, A.; Massardo, A.F. [University of Genoa, Genoa (Italy)

    2011-05-15

    This paper presents and discusses the results of a complete thermoeconomic analysis of an integrated power plant for co-production of electricity and hydrogen via pyrolysis and gasification processes fed by various coals and mixture of coal and biomass, applied to an existing large steam power plant (ENEL Brindisi power plant - 660 MWe). Two different technologies for the syngas production section are considered: pyrolysis process and direct pressurized gasification. Moreover, the proximity of a hydrogen production and purification plants to an existing steam power plant favors the inter-exchange of energy streams, mainly in the form of hot water and steam, which reduces the costs of auxiliary equipment. The high quality of the hydrogen would guarantee its usability for distributed generation and for public transport. The results were obtained using WTEMP thermoeconomic software, developed by the Thermochemical Power Group of the University of Genoa, and this project has been carried out within the framework of the FISR National project 'Integrated systems for hydrogen production and utilization in distributed power generation'.

  9. Fermentative hydrogen production from pretreated biomass: A comparative study

    NARCIS (Netherlands)

    Panagiotopoulos, I.A.; Bakker, R.R.; Budde, M.A.W.; Vrije, de G.J.; Claassen, P.A.M.; Koukios, E.G.

    2009-01-01

    The aim of this work was to evaluate the potential of employing biomass resources from different origin as feedstocks for fermentative hydrogen production. Mild-acid pretreated and hydrolysed barley straw (BS) and corn stalk (CS), hydrolysed barley grains (BG) and corn grains (CG), and sugar beet ex

  10. A Review on Patents for Hydrogen Production Using Membrane Reactors

    NARCIS (Netherlands)

    Gallucci, Fausto; Basile, Angelo; Iulianelli, Adolfo; Kuipers, J.A.M.

    2009-01-01

    Membrane reactors are a modern configuration which integrates reaction and separation units in one vessel and results in a tremendous degree of process intensification. Application of membrane reactors for hydrogen production has been widely studied in literature because membranes with infinite perm

  11. Non-thermal production of pure hydrogen from biomass: HYVOLUTION

    NARCIS (Netherlands)

    Claassen, P.A.M.; Vrije, de G.J.; Koukios, E.G.; Niel, van E.W.J.; Eroglu, I.; Modigell, M.; Friedl, A.; Wukovits, W.; Ahrer, W.

    2010-01-01

    The objectives and methodology of the EU-funded research project HYVOLUTION devoted to hydrogen production from biomass are reviewed. The main scientific objective of this project is the development of a novel two-stage bioprocess employing thermophilic and phototrophic bacteria, for the cost-effect

  12. Photobiological production of hydrogen: a solar energy conversion option

    Energy Technology Data Exchange (ETDEWEB)

    Weaver, P.; Lien, S.; Seibert, M.

    1979-01-01

    This literature survey of photobiological hydrogen production covers the period from its discovery in relatively pure cultures during the early 1930s to the present. The focus is hydrogen production by phototrophic organisms (and their components) which occurs at the expense of light energy and electron-donating substrates. The survey covers the major contributions in the area; however, in many cases, space has limited the degree of detail provided. Among the topics included is a brief historical overview of hydrogen metabolism in photosynthetic bacteria, eucaryotic algae, and cyanobacteria (blue--green algae). The primary enzyme systems, including hydrogenase and nitrogenase, are discussed along with the manner in which they are coupled to electron transport and the primary photochemistry of photosynthesis. A number of in vivo and in vitro photobiological hydrogen evolving schemes including photosynthetic bacterial, green algal, cyanobacterial, two-stage, and cell-free systems are examined in some detail. The remainder of the review discusses specific technical problem areas that currently limit the yield and duration of many of the systems and research that might lead to progress in these specific areas. The final section outlines, in broadest terms, future research directions necessary to develop practical photobiological hydrogen-producing systems. Both whole cell (near- to mid-term) and cell-free (long-term) systems should be emphasized. Photosynthetic bacteria currently show the most promise for near-term applied systems.

  13. Process development for hydrogen production with Chlamydomonas reinhardtii based on growth and product formation kinetics.

    Science.gov (United States)

    Lehr, Florian; Morweiser, Michael; Rosello Sastre, Rosa; Kruse, Olaf; Posten, Clemens

    2012-11-30

    Certain strains of microalgae are long known to produce hydrogen under anaerobic conditions. In Chlamydomonas reinhardtii the oxygen-sensitive hydrogenase enzyme recombines electrons from the chloroplast electron transport chain with protons to form molecular hydrogen directly inside the chloroplast. A sustained hydrogen production can be obtained under low sulfur conditions in C. reinhardtii, reducing the net oxygen evolution by reducing the photosystem II activity and thereby overcoming the inhibition of the hydrogenases. The development of specially adapted hydrogen production strains led to higher yields and optimized biological process preconditions. So far sustainable hydrogen production required a complete exchange of the growth medium to establish sulfur-deprived conditions after biomass growth. In this work we demonstrate the transition from the biomass growth phase to the hydrogen production phase in a single batch culture only by exact dosage of sulfur. This eliminates the elaborate and energy intensive solid-liquid separation step and establishes a process strategy to proceed further versus large scale production. This strategy has been applied to determine light dependent biomass growth and hydrogen production kinetics to assess the potential of H₂ production with C. reinhardtii as a basis for scale up and further process optimization.

  14. Biomedical and Forensic Applications of Combined Catalytic Hydrogenation-Stable Isotope Ratio Analysis

    Directory of Open Access Journals (Sweden)

    Mark A. Sephton

    2007-01-01

    Full Text Available Studies of biological molecules such as fatty acids and the steroid hormones have the potential to benefit enormously from stable carbon isotope ratio measurements of individual molecules. In their natural form, however, the body’s molecules interact too readily with laboratory equipment designed to separate them for accurate measurements to be made.Some methods overcome this problem by adding carbon to the target molecule, but this can irreversibly overprint the carbon source ‘signal’. Hydropyrolysis is a newly-applied catalytic technique that delicately strips molecules of their functional groups but retains their carbon skeletons and stereochemistries intact, allowing precise determination of the carbon source. By solving analytical problems, the new technique is increasing the ability of scientists to pinpoint molecular indicators of disease, elucidate metabolic pathways and recognise administered substances in forensic investigations.

  15. Hydrogen production by Rhodopseudomonas palustris WP 3-5 in a serial photobioreactor fed with hydrogen fermentation effluent.

    Science.gov (United States)

    Lee, Chi-Mei; Hung, Guo-Jan; Yang, Chu-Fang

    2011-09-01

    In this study, a lab-scale serial photobioreactor composed of three column reactors was constructed and continuously operated to investigate several parameters influencing photohydrogen production when using the synthetic wastewater and the anaerobic hydrogen fermentation effluents as the influents. The results indicated that better hydrogen production rate was obtained when the serial photobioreactor was operated under cellular recycling at a short HRT of 8h. The serial photobioreactor maintained high hydrogen content ca. 80% in the produced gas and 0.4× dilution ratio was the suitable ratio for hydrogen production. When the photobioreactor fed with the real wastewater (Effluent 1) containing 100 mg/L NH4Cl, Column 1 reactor successfully reduced ammonia concentration to about 60 mg/L for cell synthesis, resulting in a steady hydrogen production in the following two column reactors. The average hydrogen production rate was 205 mL-H2/L/d.

  16. Methane and hydrogen production by human intestinal anaerobic bacteria.

    Science.gov (United States)

    McKay, L F; Holbrook, W P; Eastwood, M A

    1982-06-01

    The gas above liquid cultures of a variety of human intestinal anaerobic bacteria was sampled and analysed by headspace gas chromatography. Hydrogen production was greatest with strains of the genus Clostridium, intermediate with anaerobic cocci and least with Bacteroides sp. Very few strains produced methane although small amounts were detected with one strain of B. thetaiotaomicron, C. perfringens and C. histolyticum. There may be a relationship between these anaerobic bacteria and several gastrointestinal disorders in which there is a build up of hydrogen or methane in the intestines.

  17. Electrolytic hydrogen fuel production with solid polymer electrolyte technology.

    Science.gov (United States)

    Titterington, W. A.; Fickett, A. P.

    1973-01-01

    A water electrolysis technology based on a solid polymer electrolyte (SPE) concept is presented for applicability to large-scale hydrogen production in a future energy system. High cell current density operation is selected for the application, and supporting cell test performance data are presented. Demonstrated cell life data are included to support the adaptability of the SPE system to large-size hydrogen generation utility plants as needed for bulk energy storage or transmission. The inherent system advantages of the acid SPE electrolysis technology are explained. System performance predictions are made through the year 2000, along with plant capital and operating cost projections.

  18. Photochemical production of hydrogen with zinc sulfide suspensions

    Energy Technology Data Exchange (ETDEWEB)

    Reber, J.F.; Meier, K.

    1984-11-22

    Hydrogen has been produced efficiently by the irradiation of suspensions of metalized ZnS powders in the presence of hole scavengers such as S/sup 2 -/ and SO/sub 3//sup 2 -/ions, mixtures of these two, or S/sup 2 -/ and hypophosphite ions. Results of investigation of the properties of active ZnS photocatalysts, the reaction parameters, and the formation of the reaction products are reported. The rate of the reaction was found to be strongly dependent on the amount of ZnS, and ZnS produced 5 times as much hydrogen as CdS.

  19. Large scale synthesis of CdS nanorods and its utilization in photo-catalytic H{sub 2} production

    Energy Technology Data Exchange (ETDEWEB)

    Janet, C M; Viswanath, R P [Department of Chemistry, Indian Institute of Technology Madras, Chennai-600036 (India)

    2006-10-28

    CdS nanorods along with nanostrips and plates have been prepared on a large scale by the solvothermal route using the precursor cadmium oxalate under mild conditions with ethylene glycol as the solvent and (NH{sub 4}){sub 2}S as the sulfiding agent, without using catalysts, surfactants or template. The aspect ratio of the rods varied from 3 to 30. Characterization has been done by TEM, HR-TEM, EDX, HR-SEM, XRD, BET surface area, UV-vis absorption, photoluminescence and fluorescence studies. Photo-catalytic H{sub 2} production activity was tested with as-synthesized CdS, calcined CdS, noble metal loaded CdS and for bulk CdS. The nanorods being formed are used as such for H{sub 2} production. The as-synthesized CdS is found to have very good H{sub 2} production capacity compared to that of the bulk CdS. Upon Pt loading much enhanced activity was observed in the rate of hydrogen production.

  20. Hydrogen production from methane reforming: thermodynamic assessment

    Energy Technology Data Exchange (ETDEWEB)

    Assis, A.J.; Hori, Carla E.; Avila Neto, Cicero; Franco, Tatiana [Federal University of Uberlandia (UFU), MG (Brazil). School of Chemical Engineering]. E-mail: adilsonjassis@gmail.com

    2008-07-01

    The main contributions of this study are to conduct a comparative thermodynamic analysis of methane reforming reactions and to asses the influence of key operational variables on chemical equilibrium using an in-house code, developed in the open-source software Scilab{sup c} INRIA-ENPC (www.scilab.org). Equilibrium compositions are calculated by two distinct methods: evaluation of equilibrium constants and Lagrange multipliers. Both methods result in systems of non-linear algebraic equations, solved numerically using the Scilab function 'fsolve'. Comparison between experimental and simulated equilibrium data, published in the literature, was used to validate the simulated results. Effects of temperature, pressure, initial H{sub 2}O/CH{sub 4} ratio (steam reforming), initial CH{sub 4}:CO{sub 2}:N{sub 2} ratio (dry reforming) and initial O{sub 2}/CH{sub 4} ratio (partial oxidation) on the reaction products were evaluated. (author)

  1. Production of Excited Atomic Hydrogen from Methane

    Science.gov (United States)

    Machacek, J. R.; Andrianarijaona, V. M.; Furst, J. E.; Gay, T. J.; Kilcoyne, A. L. D.; Landers, A. L.; McLaughlin, K. W.

    2009-05-01

    We have measured the production of Lyα and Hα fluorescence from atomic H for the photodissociation of CH4 by linearly-polarized photons with energies between 20 and 65 eV. Comparison between our Lyα relative cross section and that previously reported [1] show different peak height ratios. This also occurs in the Hα cross section when compared to previous data [2]. We do not observe as significant a drop in either cross section above 35 eV. Our measurements were taken with pressures two orders of magnitude lower than those used in ref. [1]. We present comparisons between data sets and a discussion of possible systematic effects. [1] H. Fukuzawa et al., J. Phys. B. 38, 565 (2005). [2] M. Kato et al., J. Phys. B. 35, 4383 (2002). Support provided by the NSF (Grant PHY-0653379), DOE (LBNL/ALS) and ANSTO (Access to Major Research Facilities Programme).

  2. Pure silica SBA-15 supported Cu-Ni catalysts for hydrogen production by ethanol steam reforming

    Energy Technology Data Exchange (ETDEWEB)

    Vizcayno, A.J.; Carrero, A.; Calles, J.A. [Department of Chemical and Environmental Technology, Rey Juan Carlos University, Escuela Superior de Ciencias Experimentales y Tecnologya (ESCET), c/ Tulipan s/n, 28933 Mostoles, (Spain)

    2006-07-01

    Cu-Ni/SBA-15 supported catalysts prepared by the incipient wetness impregnation method were tested in the ethanol steam reforming reaction for hydrogen production. The effect of reaction temperature and metal loading was studied in order to maximize the hydrogen selectivity and the CO{sub 2}/CO{sub x} molar ratio. The best catalytic performance was achieved at 600 C with a catalyst containing 2 and 7 wt% of copper and nickel, respectively. In addition, two catalysts were prepared by the method of direct insertion of Ni and Cu ions as precursors in the initial stage of the synthesis. XRD, TEM, N{sub 2} adsorption and ICP-AES results evidenced that SBA-15 materials with long range hexagonal ordering could be successfully synthesized in the presence of copper and nickel salts with the (Cu+Ni) contents around 4-6 wt%. However, lower hydrogen selectivity and together with ethanol and water conversions were observed with catalysts prepared by direct synthesis in comparison with those prepared by incipient wetness impregnation method. (authors)

  3. Rational design of ornithine decarboxylase with high catalytic activity for the production of putrescine.

    Science.gov (United States)

    Choi, Hyang; Kyeong, Hyun-Ho; Choi, Jung Min; Kim, Hak-Sung

    2014-09-01

    Putrescine finds wide industrial applications in the synthesis of polymers, pharmaceuticals, agrochemicals, and surfactants. Owing to economic and environmental concerns, the microbial production of putrescine has attracted a great deal of attention, and ornithine decarboxylase (ODC) is known to be a key enzyme in the biosynthetic pathway. Herein, we present the design of ODC from Escherichia coli with high catalytic efficiency using a structure-based rational approach. Through a substrate docking into the model structure of the enzyme, we first selected residues that might lead to an increase in catalytic activity. Of the selected residues that are located in the α-helix and the loops constituting the substrate entry site, a mutational analysis of the single mutants identified two key residues, I163 and E165. A combination of two single mutations resulted in a 62.5-fold increase in the catalytic efficiency when compared with the wild-type enzyme. Molecular dynamics simulations of the best mutant revealed that the substrate entry site becomes more flexible through mutations, while stabilizing the formation of the dimeric interface of the enzyme. Our approach can be applied to the design of other decarboxylases with high catalytic efficiency for the production of various chemicals through bio-based processes.

  4. Co-catalyst free Titanate Nanorods for improved Hydrogen production under solar light irradiation

    Indian Academy of Sciences (India)

    N Lakshmana Reddy; D Praveen Kumar; M V Shankar

    2016-04-01

    Harnessing solar energy for water splitting into hydrogen (H2) and oxygen (O2) gases in the presence of semiconductor catalyst is one of the most promising and cleaner methods of chemical fuel (H2) production. Herein, we report a simplified method for the preparation of photo-active titanate nanorods catalyst and explore the key role of calcination temperature and time period in improving catalytic properties. Both as-synthesized and calcined material showed rod-like shape and trititanate structure as evidenced from crystal structure and morphology analysis. Notably, calcination process affected both length and diameter of the nanorods into shorter and smaller size respectively. In turn, they significantly influenced the band gap reduction, resulting in visible light absorption at optimized calcination conditions. The calcined nanorods showed shift in optical absorption band edge towards longer wave length than pristine nanorods. The rate of hydrogen generation using different photocatalysts was measured by suspending trititanate nanorods (in the absence of co-catalyst) in glycerol-water mixture under solar light irradiation. Among the catalysts, nanorods calcined at 250°C for 2 hours recorded high rate of H2 production and stability confirmed for five cycles. Photocatalytic properties and plausible pathway responsible for improved H2 production are discussed in detail.

  5. Hydrogen production using thermocatalytic decomposition of methane on Ni30/activated carbon and Ni30/carbon black.

    Science.gov (United States)

    Srilatha, K; Viditha, V; Srinivasulu, D; Ramakrishna, S U B; Himabindu, V

    2016-05-01

    Hydrogen is an energy carrier of the future need. It could be produced from different sources and used for power generation or as a transport fuel which mainly in association with fuel cells. The primary challenge for hydrogen production is reducing the cost of production technologies to make the resulting hydrogen cost competitive with conventional fuels. Thermocatalytic decomposition (TCD) of methane is one of the most advantageous processes, which will meet the future demand, hence an attractive route for COx free environment. The present study deals with the production of hydrogen with 30 wt% of Ni impregnated in commercially available activated carbon and carbon black catalysts (samples coded as Ni30/AC and Ni30/CB, respectively). These combined catalysts were not attempted by previous studies. Pure form of hydrogen is produced at 850 °C and volume hourly space velocity (VHSV) of 1.62 L/h g on the activity of both the catalysts. The analysis (X-ray diffraction (XRD)) of the catalysts reveals moderately crystalline peaks of Ni, which might be responsible for the increase in catalytic life along with formation of carbon fibers. The activity of carbon black is sustainable for a longer time compared to that of activated carbon which has been confirmed by life time studies (850 °C and 54 sccm of methane).

  6. Options for nitriles removal from C{sub 4}-C{sub 5} cuts. 3. Catalytic hydrogenation using the swing reactive removal process

    Energy Technology Data Exchange (ETDEWEB)

    Ramirez-Corredores, M.M.; Hernandez, Z.; Guerra, J.; Alvarez, R.; Medina, J. [PDVSA Intevep, Refinacion y Petroquimica, Aptdo. 76343, Caracas 1070A (Venezuela)

    2003-05-15

    C{sub 4} and C{sub 5} cuts from FCC units can be useful in the preparation of oxygenates such as MTBE, ETBE, and TAME. However, these feedstocks typically contain nitriles and diolefins which poison the etherification catalyst. Albeit, in USA, strong concerns on oxygenate uses have given rise to prohibition within certain states, those concerns have not derived into such drastic decisions in Europe. Still, removing nitriles from reactive feedstocks or converting them into value-added products might be of interest. PDVSA Intevep has developed several methods for removing nitriles present in those feedstocks, which include one based on adsorption [M.M. Ramirez-Corredores, Z. Hernandez, J. Guerra, J. Medina, R. Alvarez. Submitted to Adsorption.], and two based on catalytic conversion. In the first part of this work [M.M. Ramirez-Corredores, Z. Hernandez, J. Guerra, J. Medina, R. Alvarez. Submitted to Adsorption.], both the adsorbent and the adsorption process were described. The details of the catalytic system for the simultaneous hydrogenation of nitriles and diolefins were given in the second part [M.M. Ramirez-Corredores, T. Romero, D. Djaouadi, Z. Hernandez, J. Guerra. Submitted to Ind. Eng. Chem. Res.]. The main features of the catalyst include its nitrile adsorption capabilities, the specific oxidation state of the metal active phase, and the strong early deactivation. In this work, we discuss the convenience of converting the nitriles and diolefins by using a swing mode of reaction between two (or more) reacting zones in order to overcome the drawbacks of the observed deactivation.

  7. Microbial control of hydrogen sulfide production

    Energy Technology Data Exchange (ETDEWEB)

    Montgomery, A.D.; Bhupathiraju, V.K.; Wofford, N.; McInerney, M.J. [Univ. of Oklahoma, Tulsa, OK (United States)] [and others

    1995-12-31

    A sulfide-resistant strain of Thiobacillus denitrificans, strain F, prevented the accumulation of sulfide by Desulfovibrio desulfuricans when both organisms were grown in liquid medium. The wild-type strain of T. denitrificans did not prevent the accumulation of sulfide produced by D. desulfuricans. Strain F also prevented the accumulation of sulfide by a mixed population of sulfate-reducing bacteria enriched from an oil field brine. Fermentation balances showed that strain F stoichiometrically oxidized the sulfide produced by D. desulfuricans and the oil field brine enrichment to sulfate. The ability of a strain F to control sulfide production in an experimental system of cores and formation water from the Redfield, Iowa, natural gas storage facility was also investigated. A stable, sulfide-producing biofilm was established in two separate core systems, one of which was inoculated with strain F while the other core system (control) was treated in an identical manner, but was not inoculated with strain F. When formation water with 10 mM acetate and 5 mM nitrate was injected into both core systems, the effluent sulfide concentrations in the control core system ranged from 200 to 460 {mu}M. In the test core system inoculated with strain F, the effluent sulfide concentrations were lower, ranging from 70 to 110 {mu}M. In order to determine whether strain F could control sulfide production under optimal conditions for sulfate-reducing bacteria, the electron donor was changed to lactate and inorganic nutrients (nitrogen and phosphate sources) were added to the formation water. When nutrient-supplemented formation water with 3.1 mM lactate and 10 mM nitrate was used, the effluent sulfide concentrations of the control core system initially increased to about 3,800 {mu}M, and then decreased to about 1,100 {mu}M after 5 weeks. However, in the test core system inoculated with strain F, the effluent sulfide concentrations were much lower, 160 to 330 {mu}M.

  8. Bioaugmentation of biogas production by a hydrogen-producing bacterium.

    Science.gov (United States)

    Ács, Norbert; Bagi, Zoltán; Rákhely, Gábor; Minárovics, János; Nagy, Katalin; Kovács, Kornél L

    2015-06-01

    The rate-limiting nature of the hydrogen concentration prevailing in the anaerobic digester has been recognized, but the associated alterations in the microbial community are unknown. In response to the addition of Enterobacter cloacae cells in laboratory anaerobic digesters, the level of biogas production was augmented. Terminal restriction fragment length polymorphism (T-RFLP) and real-time polymerase chain reaction (Real-Time PCR) were used to study the survival of mesophilic hydrogen-producing bacteria and the effects of their presence on the composition of the other members of the bacterial community. E. cloacae proved to maintain a stable cell number and to influence the microbial composition of the system. Bioaugmentation by a single strain added to the natural biogas-producing microbial community was demonstrated. The community underwent pronounced changes as a result of the relatively slight initial shift in the microbiological system, responding sensitively to the alterations in local hydrogen concentration.

  9. Water electrolysis for hydrogen production in Brazilian perspective

    Energy Technology Data Exchange (ETDEWEB)

    Saliba-Silva, Adonis Marcelo; Carvalho, Fatima M.S.; Bergamaschi, Vanderlei Sergio; Linardi, Marcelo [Instituto de Pesquisas Energeticas e Nucleares (CCCH/IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Fuel Cell and Hydrogen Center], Email: saliba@ipen.br

    2009-07-01

    Hydrogen is a promising energy carrier, which potentially could replace the fossil fuels used in the transportation and distributed energy sector of Brazilian economy. Fossil fuels are polluting by carbogenic emissions from their combustion, being so co-responsible for present global warming. However, no large scale, cost-effective, environmentally non-carbogenic hydrogen production process is currently available for commercialization. There are feasible possibilities to use electrolysis as one of the main sources of hydrogen, especially thinking on combination with renewable sources of energy, mainly eolic and solar. In this work some perspectives for Brazilian energy context is presented, where electrolysis combined with renewable power source and fuel cell power generation would be a good basis to improve the distributed energy supply for remote areas, where the electricity grid is not present or is deficient. (author)

  10. Sequestration of carbon dioxide with hydrogen to useful products

    Energy Technology Data Exchange (ETDEWEB)

    Adams, Michael W. W.; Kelly, Robert M.; Hawkins, Aaron B.; Menon, Angeli Lal; Lipscomb, Gina Lynette Pries; Schut, Gerrit Jan

    2017-03-07

    Provided herein are genetically engineered microbes that include at least a portion of a carbon fixation pathway, and in one embodiment, use molecular hydrogen to drive carbon dioxide fixation. In one embodiment, the genetically engineered microbe is modified to convert acetyl CoA, molecular hydrogen, and carbon dioxide to 3-hydroxypropionate, 4-hydroxybutyrate, acetyl CoA, or the combination thereof at levels greater than a control microbe. Other products may also be produced. Also provided herein are cell free compositions that convert acetyl CoA, molecular hydrogen, and carbon dioxide to 3-hydroxypropionate, 4-hydroxybutyrate, acetyl CoA, or the combination thereof. Also provided herein are methods of using the genetically engineered microbes and the cell free compositions.

  11. Hydrogen production employing Spirulina maxima 2342: A chemical analysis

    Energy Technology Data Exchange (ETDEWEB)

    Juantorena, A.U.; Santoyo, E.; Gamboa, S.A.; Lastres, O.D. [Centro de Investigacion en Energia, UNAM, Temixco 62580, Morelos (Mexico); Sebastian, P.J. [Centro de Investigacion en Energia, UNAM, Temixco 62580, Morelos (Mexico); Cuerpo Academico de Energia, UP Chiapas, Tuxtla Gutierrez, Chiapas (Mexico); Sanchez-Escamilla, D. [Instituto de Investigaciones Electricas, Cuernavaca, Morelos (Mexico); Bustos, A. [Centro de Ciencias Fisicas, UNAM, Ave. Universidad, Cuernavaca, Morelos (Mexico); Eapen, D. [Investigacion y Desarrollo en Agroindustria, UP Chiapas, Tuxtla Gutierrez, Chiapas (Mexico)

    2007-10-15

    The biomass of the cyanobacteria, Spirulina maxima 2342, was autotrophically obtained in a 20 l bioreactor under illumination and air bubbling and analyzed for its photobiological hydrogen production capability. A volume of 250 ml of Spirulina sp. taken from the reactor was used as culture sample for performing the experiments. An illumination-agitation process was employed to induce the hydrogen photoproduction reaction. The hydrogen produced in this process was quantified by gas chromatography technique using Molesieve 5 A(16ft x (1)/(8)in) column and a thermal conductivity detector (with a detector temperature of 110{sup o}C and a column temperature of 60{sup o}C). The culture samples were finally observed in an electron microscope to evaluate the effect of vacuum on the Spirulina sp. cells. (author)

  12. Hydrogen Production with Steam Reforming of Dimethyl Ether

    Institute of Scientific and Technical Information of China (English)

    Kaoru TAKEISHI; Akane ARASE

    2005-01-01

    @@ 1Introduction Steam reforming of methanol and gasoline is actively researched and developed as hydrogen supply methods for the fuel cells of vehicles and so on. However, these materials have the problems such as the infrastructure, toxicity, difficulty of the reforming, and so forth. Dimethyl ether (DME) does not contain the poisonous substances, and is expected as a clean fuel of the next generation. DME is able to take the place of light oil and LPG, and its physical properties are similar to those of LPG. There is possibility that DME infrastructures will be settled more rapidly than those of hydrogen and methanol, because LPG infrastructures existing are able to use for DME. Then, we have been studying on steam reforming of DME for the hydrogen production.

  13. Photoelectrochemical based direct conversion systems for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Kocha, S.; Peterson, M.; Arent, D. [National Renewable Energy Lab., Golden, CO (United States)] [and others

    1996-10-01

    Photon driven, direct conversion systems consist of a light absorber and a water splitting catalyst as a monolithic system; water is split directly upon illumination. This one-step process eliminates the need to generate electricity externally and subsequently feed it to an electrolyzer. These configurations require only the piping necessary for transport of hydrogen to an external storage system or gas pipeline. This work is focused on multiphoton photoelectrochemical devices for production of hydrogen directly using sunlight and water. Two types of multijunction cells, one consisting of a-Si triple junctions and the other GaInP{sub 2}/GaAs homojunctions, were studied for the photoelectrochemical decomposition of water into hydrogen and oxygen from an aqueous electrolyte solution. To catalyze the water decomposition process, the illuminated surface of the device was modified either by addition of platinum colloids or by coating with ruthenium dioxide. These colloids have been characterized by gel electrophoresis.

  14. Dynamic Simulation and Optimization of Nuclear Hydrogen Production Systems

    Energy Technology Data Exchange (ETDEWEB)

    Paul I. Barton; Mujid S. Kaximi; Georgios Bollas; Patricio Ramirez Munoz

    2009-07-31

    This project is part of a research effort to design a hydrogen plant and its interface with a nuclear reactor. This project developed a dynamic modeling, simulation and optimization environment for nuclear hydrogen production systems. A hybrid discrete/continuous model captures both the continuous dynamics of the nuclear plant, the hydrogen plant, and their interface, along with discrete events such as major upsets. This hybrid model makes us of accurate thermodynamic sub-models for the description of phase and reaction equilibria in the thermochemical reactor. Use of the detailed thermodynamic models will allow researchers to examine the process in detail and have confidence in the accurary of the property package they use.

  15. Lichen symbiosis: nature's high yielding machines for induced hydrogen production.

    Science.gov (United States)

    Papazi, Aikaterini; Kastanaki, Elizabeth; Pirintsos, Stergios; Kotzabasis, Kiriakos

    2015-01-01

    Hydrogen is a promising future energy source. Although the ability of green algae to produce hydrogen has long been recognized (since 1939) and several biotechnological applications have been attempted, the greatest obstacle, being the O2-sensitivity of the hydrogenase enzyme, has not yet been overcome. In the present contribution, 75 years after the first report on algal hydrogen production, taking advantage of a natural mechanism of oxygen balance, we demonstrate high hydrogen yields by lichens. Lichens have been selected as the ideal organisms in nature for hydrogen production, since they consist of a mycobiont and a photobiont in symbiosis. It has been hypothesized that the mycobiont's and photobiont's consumption of oxygen (increase of COX and AOX proteins of mitochondrial respiratory pathways and PTOX protein of chrolorespiration) establishes the required anoxic conditions for the activation of the phycobiont's hydrogenase in a closed system. Our results clearly supported the above hypothesis, showing that lichens have the ability to activate appropriate bioenergetic pathways depending on the specific incubation conditions. Under light conditions, they successfully use the PSII-dependent and the PSII-independent pathways (decrease of D1 protein and parallel increase of PSaA protein) to transfer electrons to hydrogenase, while under dark conditions, lichens use the PFOR enzyme and the dark fermentative pathway to supply electrons to hydrogenase. These advantages of lichen symbiosis in combination with their ability to survive in extreme environments (while in a dry state) constitute them as unique and valuable hydrogen producing natural factories and pave the way for future biotechnological applications.

  16. Lichen symbiosis: nature's high yielding machines for induced hydrogen production.

    Directory of Open Access Journals (Sweden)

    Aikaterini Papazi

    Full Text Available Hydrogen is a promising future energy source. Although the ability of green algae to produce hydrogen has long been recognized (since 1939 and several biotechnological applications have been attempted, the greatest obstacle, being the O2-sensitivity of the hydrogenase enzyme, has not yet been overcome. In the present contribution, 75 years after the first report on algal hydrogen production, taking advantage of a natural mechanism of oxygen balance, we demonstrate high hydrogen yields by lichens. Lichens have been selected as the ideal organisms in nature for hydrogen production, since they consist of a mycobiont and a photobiont in symbiosis. It has been hypothesized that the mycobiont's and photobiont's consumption of oxygen (increase of COX and AOX proteins of mitochondrial respiratory pathways and PTOX protein of chrolorespiration establishes the required anoxic conditions for the activation of the phycobiont's hydrogenase in a closed system. Our results clearly supported the above hypothesis, showing that lichens have the ability to activate appropriate bioenergetic pathways depending on the specific incubation conditions. Under light conditions, they successfully use the PSII-dependent and the PSII-independent pathways (decrease of D1 protein and parallel increase of PSaA protein to transfer electrons to hydrogenase, while under dark conditions, lichens use the PFOR enzyme and the dark fermentative pathway to supply electrons to hydrogenase. These advantages of lichen symbiosis in combination with their ability to survive in extreme environments (while in a dry state constitute them as unique and valuable hydrogen producing natural factories and pave the way for future biotechnological applications.

  17. Promoted Ru on high-surface area graphite for efficient miniaturized production of hydrogen from ammonia

    DEFF Research Database (Denmark)

    Sørensen, Rasmus Zink; Klerke, Asbjørn; Quaade, Ulrich

    2006-01-01

    Promoted Ru/C catalysts for decomposition of ammonia are incorporated into micro-fabricated reactors for the first time. With the reported preparation technique, the performance is increased more than two orders of magnitude compared to previously known micro-fabricated reactors for ammonia decom...... studies of both ammonia synthesis and decomposition, and it is shown how proper promotion can facilitate ammonia decomposition at temperatures below 500 K.......Promoted Ru/C catalysts for decomposition of ammonia are incorporated into micro-fabricated reactors for the first time. With the reported preparation technique, the performance is increased more than two orders of magnitude compared to previously known micro-fabricated reactors for ammonia...... decomposition. The catalytic activities for production of hydrogen from ammonia are determined for different promoters and promoter levels on graphite supported ruthenium catalysts. The reactivity trends of the Ru/C catalysts promoted with Cs and Ba are in excellent agreement with those known from earlier...

  18. Apparatus for hydrogen and carbon production via carbon aerosol-catalyzed dissociation of hydrocarbons

    Science.gov (United States)

    Muradov, Nazim Z. (Inventor); Smith, Franklyn (Inventor); Tabatabaie-Raissi, Ali (Inventor)

    2012-01-01

    A novel process and apparatus is disclosed for sustainable, continuous production of hydrogen and carbon by catalytic dissociation or decomposition of hydrocarbons at elevated temperatures using in-situ generated carbon particles. Carbon particles are produced by decomposition of carbonaceous materials in response to an energy input. The energy input can be provided by at least one of a non-oxidative and oxidative means. The non-oxidative means of the energy input includes a high temperature source, or different types of plasma, such as, thermal, non-thermal, microwave, corona discharge, glow discharge, dielectric barrier discharge, or radiation sources, such as, electron beam, gamma, ultraviolet (UV). The oxidative means of the energy input includes oxygen, air, ozone, nitrous oxide (NO.sub.2) and other oxidizing agents. The method, apparatus and process of the present invention is applicable to any gaseous or liquid hydrocarbon fuel and it produces no or significantly less CO.sub.2 emissions compared to conventional processes.

  19. Multistage Extractive Reaction for Hydrogen Peroxide Production by Anthraquinone Process

    Institute of Scientific and Technical Information of China (English)

    WANG Li; L(U) Shuxiang; WANG Yaquan; MI Zhentao

    2005-01-01

    The extractive reaction process of oxygen-working solution-water three-phase system for the production of hydrogen peroxide by the anthraquinone method was investigated in a sieve plate column of 50 mm in internal diameter. The oxidation reaction of anthrahydroquinone in the working solution with oxygen and the extraction of hydrogen peroxide from the working solution into aqueous phase occurred simultaneously in the countercurrent mode. The agitating effect caused by gaseous phase made the droplets of the dispersed phase become smaller, thus, increasing the liquid-liquid interfacial contact areas and resulting in the improvement of the mass transfer velocity. Results showed that the gas-agitation had a beneficial effect on the extraction of hydrogen peroxide from the working solution into the aqueous phase; the concentration of hydrogen peroxide in the raffinate decreased with the increase of the gaseous superficial velocities; and the concentration of H2O2 in the raffinate increased with the increase of the dispersed phase superficial velocity at the same superficial velocity of the gaseous phase. In the G-L-L extractive reaction process, with the increase of the gaseous superficial velocities, both the conversion of the anthrahydroquinone oxidation and the extraction efficiency of hydrogen peroxide first increased significantly, then increased gradually.

  20. Hydrogen production from the monomeric sugars hydrolyzed from hemicellulose by Enterobacter aerogenes

    Energy Technology Data Exchange (ETDEWEB)

    Ren, Yunli; Wang, Jianji; Liu, Zhen; Ren, Yunlai; Li, Guozhi [School of Chemical Engineering and Pharmaceutics, Henan University of Science and Technology, Luoyang 471039, Henan (China)

    2009-12-15

    Relatively large percentages of xylose with glucose, arabinose, mannose, galactose and rhamnose constitute the hydrolysis products of hemicellulose. In this paper, hydrogen production performance of facultative anaerobe (Enterobacter aerogenes) has been investigated from these different monomeric sugars except glucose. It was shown that the stereoisomers of mannose and galactose were more effective for hydrogen production than those of xylose and arabinose. The substrate of 5 g/l xylose resulted in a relative high level of hydrogen yield (73.8 mmol/l), hydrogen production efficiency (2.2 mol/mol) and a maximum hydrogen production rate (249 ml/l/h). The hydrogen yield, hydrogen production efficiency and the maximum hydrogen production rate reached 104 mmol/l, 2.35 mol/mol and 290 ml/l/h, respectively, on a substrate of 10 g/l galactose. The hydrogen yields and the maximum hydrogen production rates increased with an increase of mannose concentrations and reached 119 mmol/l and 518 ml/l/h on the culture of 25 g/l mannose. However, rhamnose was a relative poor carbon resource for E. aerogenes to produce hydrogen, from which the hydrogen yield and hydrogen production efficiency were about one half of that from the mannose substrate. E. aerogenes was found to be a promising strain for hydrogen production from hydrolysis products of hemicellulose. (author)