Steam reformer with catalytic combustor

Science.gov (United States)

Voecks, Gerald E. (Inventor)

1990-01-01

A steam reformer is disclosed having an annular steam reforming catalyst bed formed by concentric cylinders and having a catalytic combustor located at the center of the innermost cylinder. Fuel is fed into the interior of the catalytic combustor and air is directed at the top of the combustor, creating a catalytic reaction which provides sufficient heat so as to maintain the catalytic reaction in the steam reforming catalyst bed. Alternatively, air is fed into the interior of the catalytic combustor and a fuel mixture is directed at the top. The catalytic combustor provides enhanced radiant and convective heat transfer to the reformer catalyst bed.

Engineering Study for a Full Scale Demonstration of Steam Reforming Black Liquor Gasification at Georgia-Pacific's Mill in Big Island, Virginia; FINAL

International Nuclear Information System (INIS)

Robert De Carrera; Mike Ohl

2002-01-01

Georgia-Pacific Corporation performed an engineering study to determine the feasibility of installing a full-scale demonstration project of steam reforming black liquor chemical recovery at Georgia-Pacific's mill in Big Island, Virginia. The technology considered was the Pulse Enhanced Steam Reforming technology that was developed and patented by Manufacturing and Technology Conversion, International (MTCI) and is currently licensed to StoneChem, Inc., for use in North America. Pilot studies of steam reforming have been carried out on a 25-ton per day reformer at Inland Container's Ontario, California mill and on a 50-ton per day unit at Weyerhaeuser's New Bern, North Carolina mill

Improvements of reforming performance of a nuclear heated steam reforming process

International Nuclear Information System (INIS)

Hada, Kazuhiko

1996-10-01

Performance of an energy production process by utilizing high temperature nuclear process heat was not competitive to that by utilizing non-nuclear process heat, especially fossil-fired process heat due to its less favorable chemical reaction conditions. Less favorable conditions are because a temperature of the nuclear generated heat is around 950degC and the heat transferring fluid is the helium gas pressurized at around 4 MPa. Improvements of reforming performance of nuclear heated steam reforming process were proposed in the present report. The steam reforming process, one of hydrogen production processes, has the possibility to be industrialized as a nuclear heated process as early as expected, and technical solutions to resolve issues for coupling an HTGR with the steam reforming system are applicable to other nuclear-heated hydrogen production systems. The improvements are as follows: As for the steam reformer, (1) increase in heat input to process gas by applying a bayonet type of reformer tubes and so on, (2) increase in reforming temperature by enhancing heat transfer rate by the use of combined promoters of orifice baffles, cylindrical thermal radiation pipes and other proposal, and (3) increase in conversion rate of methane to hydrogen by optimizing chemical compositions of feed process gas. Regarding system arrangement, a steam generator and superheater are set in the helium loop as downstream coolers of the steam reformer, so as to effectively utilize the residual nuclear heat for generating feed steam. The improvements are estimated to achieve the hydrogen production rate of approximately 3800 STP-m 3 /h for the heat source of 10 MW and therefore will provide the potential competitiveness to a fossil-fired steam reforming process. Those improvements also provide the compactness of reformer tubes, giving the applicability of seamless tubes. (J.P.N.)

Steam reforming of methane over Pt/Rh based wire mesh catalyst in single channel reformer for small scale syngas production

DEFF Research Database (Denmark)

Sigurdsson, Haftor Örn; Kær, Søren Knudsen

2012-01-01

of a catalytic parallel plate type heat exchanger (CPHE) reformer stack, where coated Pt/Rh based wire mesh is used as a catalyst. Heat is supplied to the endothermic reaction with infrared electric heaters. All the experiments were performed under atmospheric pressure and at stable operating conditions......The purpose of this study is to investigate a small scale steam methane reformer for syngas production for a micro combined heat and power (mCPH) unit under different operational conditions. The study presents an experimental analysis of the performance of a specially built single channel...... to evaluate the effect of flow maldistribution in a CPHE reformer stack on the CH4 conversion and H2 yield....

Steam reforming as a method to treat Hanford underground storage tank (UST) wastes

International Nuclear Information System (INIS)

Miller, J.E.; Kuehne, P.B.

1995-07-01

This report summarizes a Sandia program that included partnerships with Lawrence Livermore National Laboratory and Synthetica Technologies, Inc. to design and test a steam reforming system for treating Hanford underground storage tank (UST) wastes. The benefits of steam reforming the wastes include the resolution of tank safety issues and improved radionuclide separations. Steam reforming destroys organic materials by first gasifying, then reacting them with high temperature steam. Tests indicate that up to 99% of the organics could be removed from the UST wastes by steam exposure. In addition, it was shown that nitrates in the wastes could be destroyed by steam exposure if they were first distributed as a thin layer on a surface. High purity alumina and nickel alloys were shown to be good candidates for materials to be used in the severe environment associated with steam reforming the highly alkaline, high nitrate content wastes. Work was performed on designing, building, and demonstrating components of a 0.5 gallon per minute (gpm) system suitable for radioactive waste treatment. Scale-up of the unit to 20 gpm was also considered and is feasible. Finally, process demonstrations conducted on non-radioactive waste surrogates were carried out, including a successful demonstration of the technology at the 0.1 gpm scale

Bench-Scale Silicone Process for Low-Cost CO{sub 2} Capture

Energy Technology Data Exchange (ETDEWEB)

Wood, Benjamin; Genovese, Sarah; Perry, Robert; Spiry, Irina; Farnum, Rachael; Sing, Surinder; Wilson, Paul; Buckley, Paul; Acharya, Harish; Chen, Wei; McDermott, John; Vipperia, Ravikumar; Yee, Michael; Steele, Ray; Fresia, Megan; Vogt, Kirk

2013-12-31

A bench-scale system was designed and built to test an aminosilicone-based solvent. A model was built of the bench-scale system and this model was scaled up to model the performance of a carbon capture unit, using aminosilicones, for CO{sub 2} capture and sequestration (CCS) for a pulverized coal (PC) boiler at 550 MW. System and economic analysis for the carbon capture unit demonstrates that the aminosilicone solvent has significant advantages relative to a monoethanol amine (MEA)-based system. The CCS energy penalty for MEA is 35.9% and the energy penalty for aminosilicone solvent is 30.4% using a steam temperature of 395 °C (743 °F). If the steam temperature is lowered to 204 °C (400 °F), the energy penalty for the aminosilicone solvent is reduced to 29%. The increase in cost of electricity (COE) over the non-capture case for MEA is ~109% and increase in COE for aminosilicone solvent is ~98 to 103% depending on the solvent cost at a steam temperature of 395 °C (743 °F). If the steam temperature is lowered to 204 °C (400 °F), the increase in COE for the aminosilicone solvent is reduced to ~95-100%.

First principles calculations and experimental insight into methane steam reforming over transition metal catalysts

DEFF Research Database (Denmark)

Jones, Glenn; Jakobsen, Jon Geest; Shim, Signe Sarah

2008-01-01

This paper presents a detailed analysis of the steam reforming process front first-principles calculations, supported by insight from experimental investigations. In the present work we employ recently recognised scaling relationships for adsorption energies of simple molecules adsorbed at pure...... metal Surfaces to develop an overview of the steam reforming process catalyzed by a range of transition metal surfaces. By combining scaling relationships with thermodynamic and kinetic analysis, we show that it is possible to determine the reactivity trends of the pure metals for methane steam...... in situ TEM measurements under a hydrogen atmosphere. The overall agreement between theory and experiment (at 773 K, 1 bar pressure and 10% conversion) is found to be excellent with Ru and Rh being the most active pure transition metals for methane steam reforming, while Ni, Ir, Pt, and Pd...

Steam Reformer With Fibrous Catalytic Combustor

Science.gov (United States)

Voecks, Gerald E.

1987-01-01

Proposed steam-reforming reactor derives heat from internal combustion on fibrous catalyst. Supplies of fuel and air to combustor controlled to meet demand for heat for steam-reforming reaction. Enables use of less expensive reactor-tube material by limiting temperature to value safe for material yet not so low as to reduce reactor efficiency.

Development of ATSR (Auto Thermal Steam Reformer)

International Nuclear Information System (INIS)

Ono, J.; Yoshino, Y.; Kuwabara, T.; Fujisima, S.; Kobayashi, S.; Maruko, S.

2004-01-01

'Full text:' Auto-thermal reformers are used popularly for fuel cell vehicle because they are compact and can start up quickly. On the other hand, steam reformers are used for stationary fuel cell power plant because they are good thermal efficiency. While, there are many cases using the auto- thermal reformer for stationary use with expectation of cost reduction in USA, as well. However, they are still insufficient for its durability, compactness and cost. We have been developing the new type of fuel processing system that is auto-thermal steam reformer (ATSR), which is hybrid of a conventional steam reformer (STR) and a conventional auto-thermal reformer (ATR). In this study, some proto-type of ATSR for field test were designed, tried manufacturing and tested performance and durability. And we have tried to operate with fuel cell stack to evaluate the system interface performance, that is, operability and controllability. (author)

Investigations on a new internally-heated tubular packed-bed methanol–steam reformer

KAUST Repository

Nehe, Prashant; Vanteru, Mahendra Reddy; Kumar, Sudarshan

2015-01-01

Small-scale reformers for hydrogen production through steam reforming of methanol can provide an alternative solution to the demand of continuous supply of hydrogen gas for the operation of Proton Exchange Membrane Fuel Cells (PEMFCs). A packed

Hydrogen-rich gas production from waste plastics by pyrolysis and low-temperature steam reforming over a ruthenium catalyst

International Nuclear Information System (INIS)

Namioka, Tomoaki; Saito, Atsushi; Inoue, Yukiharu; Park, Yeongsu; Min, Tai-jin; Roh, Seon-ah; Yoshikawa, Kunio

2011-01-01

Operating conditions for low-temperature pyrolysis and steam reforming of plastics over a ruthenium catalyst were investigated. In the range studied, the highest gas and lowest coke fractions for polystyrene (PS) with a 60 g h -1 scale, continuous-feed, two-stage gasifier were obtained with a pyrolyzer temperature of 673 K, steam reforming temperature of 903 K, and weight hourly space velocity (WHSV) of 0.10 g-sample g-catalyst -1 h -1 . These operating conditions are consistent with optimum conditions reported previously for polypropylene. Our results indicate that at around 903 K, the activity of the ruthenium catalyst was high enough to minimize the difference between the rates of the steam reforming reactions of the pyrolysates from polystyrene and polypropylene. The proposed system thus has the flexibility to compensate for differences in chemical structures of municipal waste plastics. In addition, the steam reforming temperature was about 200 K lower than the temperature used in a conventional Ni-catalyzed process for the production of hydrogen. Low-temperature steam reforming allows for lower thermal input to the steam reformer, which results in an increase in thermal efficiency in the proposed process employing a Ru catalyst. Because low-temperature steam reforming can be also expected to reduce thermal degradation rates of the catalyst, the pyrolysis-steam reforming process with a Ru catalyst has the potential for use in small-scale production of hydrogen-rich gas from waste plastics that can be used for power generation.

Steam hydrocarbon cracking and reforming

NARCIS (Netherlands)

Golombok, M.

2004-01-01

Many industrial chemical processes are taught as distinct contrasting reactions when in fact the unifying comparisons are greater than the contrasts. We examine steam hydrocarbon reforming and steam hydrocarbon cracking as an example of two processes that operate under different chemical reactivity

Two-dimensional thermal analysis of radial heat transfer of monoliths in small-scale steam methane reforming

DEFF Research Database (Denmark)

Cui, Xiaoti; Kær, Søren Knudsen

2018-01-01

Monolithic catalysts have received increasing attention for application in the small-scale steam methane reforming process. The radial heat transfer behaviors of monolith reformers were analyzed by two-dimensional computational fluid dynamic (CFD) modeling. A parameter study was conducted...... by a large number of simulations focusing on the thermal conductivity of the monolith substrate, washcoat layer, wall gap, radiation heat transfer and the geometric parameters (cell density, porosity and diameter of monolith). The effective radial thermal conductivity of the monolith structure, kr......,eff, showed good agreement with predictions made by the pseudo-continuous symmetric model. This influence of the radiation heat transfer is low for highly conductive monoliths. A simplified model has been developed to evaluate the importance of radiation for monolithic reformers under different conditions...

Investigations on a new internally-heated tubular packed-bed methanol–steam reformer

KAUST Repository

Nehe, Prashant

2015-05-01

Small-scale reformers for hydrogen production through steam reforming of methanol can provide an alternative solution to the demand of continuous supply of hydrogen gas for the operation of Proton Exchange Membrane Fuel Cells (PEMFCs). A packed-bed type reformer is one of the potential designs for such purpose. An externally heated reformer has issues of adverse lower temperature in the core of the reformer and significant heat loss to the environment thus impacting its performance. Experimental and numerical studies on a new concept of internally heated tubular packed-bed methanol-steam reformer have been reported in this paper with improved performance in terms of higher methanol conversion and reduced heat losses to surroundings. CuO/ZnO/Al2O3 is used as the catalyst for the methanol-steam reforming reaction and a rod-type electric heater at the center of the reactor is used for supplying necessary heat for endothermic steam reforming reaction. The vaporizer and the reformer unit with a constant volume catalyst bed are integrated in the annular section of a tubular reformer unit. The performance of the reformer was investigated at various operating conditions like feed rate of water-methanol mixture, mass of the catalyst and reforming temperature. The experimental and numerical results show that the methanol conversion and CO concentration increase with internal heating for a wide range of operating conditions. The developed reformer unit generates 50-80W (based on lower heating value) of hydrogen gas for applications in PEMFCs. For optimized design and operating conditions, the reformer unit produced 298sccm reformed gas containing 70% H2, 27% CO2 and 3% CO at 200-240°C which can produce a power output of 25-32W assuming 60% fuel cell efficiency and 80% of hydrogen utilization in a PEMFC. © 2015 Hydrogen Energy Publications, LLC.

Steam reforming of technical bioethanol for hydrogen production

DEFF Research Database (Denmark)

Rass-Hansen, Jeppe; Johansson, Roger; Møller, Martin Hulbek

2008-01-01

Essentially all work on ethanol steam reforming so far has been carried out using simulated bioethanol feedstocks, which means pure ethanol mixed with water. However, technical bioethanol consists of a lot of different components including sugars, which cannot be easily vaporized and steam reformed....... For ethanol steam reforming to be of practical interest, it is important to avoid the energy-intensive purification steps to fuel grade ethanol. Therefore, it is imperative to analyze how technical bioethanol, with the relevant impurities, reacts during the steam reforming process. We show how three different...... bioethanol will result in a faster catalyst deactivation than what is observed when using pure ethanol-water mixtures because of contaminants remaining in the feed. However, the initial activity of the catalysts are not affected by this, hence it is important to not only focus on catalyst activity but rather...

Development and validation of a CFD-based steam reformer model

DEFF Research Database (Denmark)

Kær, Søren Knudsen; Dahlqvist, Mathis; Saksager, Anders

2006-01-01

Steam reforming of liquid biofuels (ethanol, bio-diesel etc.) represents a sustainable source of hydrogen for micro Combined Heat and Power (CHP) production as well as Auxiliary Power Units (APUs). In relation to the design of the steam reforming reactor several parameter are important including...... for expensive prototypes. This paper presents an advanced Computational Fluid Dynamics based model of a steam reformer. The model was implemented in the commercial CFD code Fluent through the User Defined Functions interface. The model accounts for the flue gas flow as well as the reformate flow including...... a detailed mechanism for the reforming reactions. Heat exchange between the flue gas and reformate streams through the reformer reactor walls was also included as a conjugate heat transfer process.  From a review of published models for the catalytic steam reforming of ethanol and preliminary predictions...

Steam Reforming of Bio-oil Model Compounds

DEFF Research Database (Denmark)

Trane, Rasmus; Jensen, Anker Degn; Dahl, Søren

The steam reforming of bio-oil is a sustainable and renewable route to synthesis gas and hydrogen, where one of the main hurdles is carbon formation on the catalyst.......The steam reforming of bio-oil is a sustainable and renewable route to synthesis gas and hydrogen, where one of the main hurdles is carbon formation on the catalyst....

Radial Microchannel Reactor (RMR) used in Steam Reforming CH4

Science.gov (United States)

2013-05-13

steam reforming natural gas for a wide variety of application from distributed energy production...into synthesis gas . Synthesis gas is used in the production of hydrogen , in GTL and other chemical processes. Steam reforming in an RMR was studied...technology has the potential to have a transformational reduction in cost and size of steam reforming natural gas for a wide variety of application

Steam Methane Reformation Testing for Air-Independent Solid Oxide Fuel Cell Systems

Science.gov (United States)

Mwara, Kamwana N.

2015-01-01

Recently, NASA has been looking into utilizing landers that can be propelled by LOX-CH (sub 4), to be used for long duration missions. Using landers that utilize such propellants, also provides the opportunity to use solid oxide fuel cells as a power option, especially since they are able to process methane into a reactant through fuel reformation. One type of reformation, called steam methane reformation, is a process to reform methane into a hydrogen-rich product by reacting methane and steam (fuel cell exhaust) over a catalyst. A steam methane reformation system could potentially use the fuel cell's own exhaust to create a reactant stream that is hydrogen-rich, and requires less internal reforming of the incoming methane. Also, steam reformation may hold some advantages over other types of reforming, such as partial oxidation (PROX) reformation. Steam reformation does not require oxygen, while up to 25 percent can be lost in PROX reformation due to unusable CO (sub 2) reformation. NASA's Johnson Space Center has conducted various phases of steam methane reformation testing, as a viable solution for in-space reformation. This has included using two different types of catalysts, developing a custom reformer, and optimizing the test system to find the optimal performance parameters and operating conditions.

Sintering of nickel steam reforming catalysts

DEFF Research Database (Denmark)

Sehested, Jens; Larsen, Niels Wessel; Falsig, Hanne

2014-01-01

. In this paper, particle migration and coalescence in nickel steam reforming catalysts is studied. Density functional theory calculations indicate that Ni-OH dominate nickel transport at nickel surfaces in the presence of steam and hydrogen as Ni-OH has the lowest combined energies of formation and diffusion...

Radioactive Demonstration Of Final Mineralized Waste Forms For Hanford Waste Treatment Plant Secondary Waste By Fluidized Bed Steam Reforming Using The Bench Scale Reformer Platform

International Nuclear Information System (INIS)

Crawford, C.; Burket, P.; Cozzi, A.; Daniel, W.; Jantzen, C.; Missimer, D.

2012-01-01

. The mineral waste form that is produced by co-processing waste with kaolin clay in an FBSR process has been shown to be as durable as LAW glass. Monolithing of the granular FBSR product is being investigated to prevent dispersion during transport or burial/storage, but is not necessary for performance. A Benchscale Steam Reformer (BSR) was designed and constructed at the SRNL to treat actual radioactive wastes to confirm the findings of the non-radioactive FBSR pilot scale tests and to qualify the waste form for applications at Hanford. BSR testing with WTP SW waste surrogates and associated analytical analyses and tests of granular products (GP) and monoliths began in the Fall of 2009, and then was continued from the Fall of 2010 through the Spring of 2011. Radioactive testing commenced in 2010 with a demonstration of Hanford's WTP-SW where Savannah River Site (SRS) High Level Waste (HLW) secondary waste from the Defense Waste Processing Facility (DWPF) was shimmed with a mixture of 125/129 I and 99 Tc to chemically resemble WTP-SW. Prior to these radioactive feed tests, non-radioactive simulants were also processed. Ninety six grams of radioactive granular product were made for testing and comparison to the non-radioactive pilot scale tests. The same mineral phases were found in the radioactive and non-radioactive testing.

Steam reforming of ethanol

DEFF Research Database (Denmark)

Trane-Restrup, Rasmus; Dahl, Søren; Jensen, Anker Degn

2013-01-01

Steam reforming (SR) of oxygenated species like bio-oil or ethanol can be used to produce hydrogen or synthesis gas from renewable resources. However, deactivation due to carbon deposition is a major challenge for these processes. In this study, different strategies to minimize carbon deposition...

Steam Reforming of Low-Level Mixed Waste

Energy Technology Data Exchange (ETDEWEB)

None

1998-01-01

Under DOE Contract No. DE-AR21-95MC32091, Steam Reforming of Low-Level Mixed Waste, ThermoChem has successfully designed, fabricated and operated a nominal 90 pound per hour Process Development Unit (PDU) on various low-level mixed waste surrogates. The design construction, and testing of the PDU as well as performance and economic projections for a 500- lb/hr demonstration and commercial system are described. The overall system offers an environmentally safe, non-incinerating, cost-effective, and publicly acceptable method of processing LLMW. The steam-reforming technology was ranked the No. 1 non-incineration technology for destruction of hazardous organic wastes in a study commissioned by the Mixed Waste Focus Area published April 1997.1 The ThermoChem steam-reforming system has been developed over the last 13 years culminating in this successful test campaign on LLMW surrogates. Six surrogates were successfidly tested including a 750-hour test on material simulating a PCB- and Uranium- contaminated solid waste found at the Portsmouth Gaseous Diffusion Plant. The test results indicated essentially total (>99.9999oA) destruction of RCRA and TSCA hazardous halogenated organics, significant levels of volume reduction (> 400 to 1), and retention of radlonuclides in the volume-reduced solids. Cost studies have shown the steam-reforming system to be very cost competitive with more conventional and other emerging technologies.

RADIOACTIVE DEMONSTRATION OF FINAL MINERALIZED WASTE FORMS FOR HANFORD WASTE TREATMENT PLANT SECONDARY WASTE BY FLUIDIZED BED STEAM REFORMING USING THE BENCH SCALE REFORMER PLATFORM

Energy Technology Data Exchange (ETDEWEB)

Crawford, C.; Burket, P.; Cozzi, A.; Daniel, W.; Jantzen, C.; Missimer, D.

2012-02-02

ceramic (mineral) waste form. The mineral waste form that is produced by co-processing waste with kaolin clay in an FBSR process has been shown to be as durable as LAW glass. Monolithing of the granular FBSR product is being investigated to prevent dispersion during transport or burial/storage, but is not necessary for performance. A Benchscale Steam Reformer (BSR) was designed and constructed at the SRNL to treat actual radioactive wastes to confirm the findings of the non-radioactive FBSR pilot scale tests and to qualify the waste form for applications at Hanford. BSR testing with WTP SW waste surrogates and associated analytical analyses and tests of granular products (GP) and monoliths began in the Fall of 2009, and then was continued from the Fall of 2010 through the Spring of 2011. Radioactive testing commenced in 2010 with a demonstration of Hanford's WTP-SW where Savannah River Site (SRS) High Level Waste (HLW) secondary waste from the Defense Waste Processing Facility (DWPF) was shimmed with a mixture of {sup 125/129}I and {sup 99}Tc to chemically resemble WTP-SW. Prior to these radioactive feed tests, non-radioactive simulants were also processed. Ninety six grams of radioactive granular product were made for testing and comparison to the non-radioactive pilot scale tests. The same mineral phases were found in the radioactive and non-radioactive testing.

Hydrogen generation utilizing integrated CO2 removal with steam reforming

Science.gov (United States)

Duraiswamy, Kandaswamy; Chellappa, Anand S

2013-07-23

A steam reformer may comprise fluid inlet and outlet connections and have a substantially cylindrical geometry divided into reforming segments and reforming compartments extending longitudinally within the reformer, each being in fluid communication. With the fluid inlets and outlets. Further, methods for generating hydrogen may comprise steam reformation and material adsorption in one operation followed by regeneration of adsorbers in another operation. Cathode off-gas from a fuel cell may be used to regenerate and sweep the adsorbers, and the operations may cycle among a plurality of adsorption enhanced reformers to provide a continuous flow of hydrogen.

Thermal and chemical analysis on steam reforming in an out-of-pile test facility (Contract research)

Energy Technology Data Exchange (ETDEWEB)

Haga, Katsuhiro [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment; Suyama, Kazumasa; Inagaki, Yoshiyuki; Hayashi, Kohji; Ogawa, Masuro

1999-08-01

An out-of-pile test facility of a hydrogen production system whose scale is 1/30th of the HTTR hydrogen production system is presently under construction at the Oarai Establishment of the Japan Atomic Energy Research Institute. In this system, a steam generator works as a thermal buffer for mitigating the heat consumption fluctuation in a steam reformer so as not to affect an operation of the reactor system. To control the thermal buffer system properly, it is important to evaluate the effect of the steam reforming parameters on the heat fluctuation in advance. So, using the mass and thermal balance analysis code developed for a simulation of the out-of-pile test facility, the heat consumption fluctuation in the steam reformer was analyzed by various changes of the process gas flow rate, the process gas inlet temperature, the process gas composition etc. From the analytical results, it was found that the heat transfer augmentation of the reformer tube by using repeated fins was effective in increasing the hydrogen production rate of up to 12.5%. Also, the fluctuation of the process gas flow rate tended to greatly affect the heat consumption rate for the steam reforming reaction, so that the helium gas temperature increased from 586degC to 718degC. (author)

Steam reforming of biomass derived oxygenates to hydrogen : Importance of metal-support boundary

NARCIS (Netherlands)

Takanabe, K.; Aika, Ken-ichi; Seshan, Kulathu Iyer; Lefferts, L.

2006-01-01

Steam reforming of acetic acid over Pt/ZrO2 catalysts was studied as a model reaction of steam reforming of biomass derived oxygenates. Pt/ZrO2 catalysts were very active; however, the catalyst deactivated in time by formation of oligomers which block the active sites for steam reforming.

In-Space Propulsion, Logistics Reduction, and Evaluation of Steam Reformer Kinetics: Problems and Prospects

Science.gov (United States)

Jaworske, D. A.; Palaszewski, B. A.; Kulis, M. J.; Gokoglu, S. A.

2015-01-01

Human space missions generate waste materials. A 70-kg crewmember creates a waste stream of 1 kg per day, and a four-person crew on a deep space habitat for a 400+ day mission would create over 1600 kg of waste. Converted into methane, the carbon could be used as a fuel for propulsion or power. The NASA Advanced Exploration Systems (AES) Logistics Reduction and Repurposing (LRR) project is investing in space resource utilization with an emphasis on repurposing logistics materials for useful purposes and has selected steam reforming among many different competitive processes as the preferred method for repurposing organic waste into methane. Already demonstrated at the relevant processing rate of 5.4 kg of waste per day, high temperature oxygenated steam consumes waste and produces carbon dioxide, carbon monoxide, and hydrogen which can then be converted into methane catalytically. However, the steam reforming process has not been studied in microgravity. Data are critically needed to understand the mechanisms that allow use of steam reforming in a reduced gravity environment. This paper reviews the relevant literature, identifies gravity-dependent mechanisms within the steam gasification process, and describes an innovative experiment to acquire the crucial kinetic information in a small-scale reactor specifically designed to operate within the requirements of a reduced gravity aircraft flight. The experiment will determine if the steam reformer process is mass-transport limited, and if so, what level of forced convection will be needed to obtain performance comparable to that in 1-g.

Methane-steam reforming by molten salt - membrane reactor using concentrated solar thermal energy

International Nuclear Information System (INIS)

Watanuki, K.; Nakajima, H.; Hasegawa, N.; Kaneko, H.; Tamaura, Y.

2006-01-01

By utilization of concentrated solar thermal energy for steam reforming of natural gas, which is an endothermic reaction, the chemical energy of natural gas can be up-graded. The chemical system for steam reforming of natural gas with concentrated solar thermal energy was studied to produce hydrogen by using the thermal storage with molten salt and the membrane reactor. The original steam reforming module with hydrogen permeable palladium membrane was developed and fabricated. Steam reforming of methane proceeded with the original module with palladium membrane below the decomposition temperature of molten salt (around 870 K). (authors)

Design of a nuclear steam reforming plant

International Nuclear Information System (INIS)

Malherbe, J.

1980-01-01

The design of a plant for the steam reforming of methane using a High Temperature Reactor has been studied by CEA in connection with the G.E.G.N. This group of companies (CEA, GAZ DE FRANCE, CHARBONNAGES DE FRANCE, CREUSOT-LOIRE, NOVATOME) is in charge of studying the feasibility of the coal gasification process by using a nuclear reactor. The process is based on the hydrogenation of the coal in liquid phase with hydrogen produced by a methane steam reformer. The reformer plant is fed by a pipe of natural gas or SNG. The produced hydrogen feeds the gasification plant which could not be located on the same site. An intermediate hydrogen storage between the two plants could make the coupling more flexible. The gasification plant does not need a great deal of heat and this heat can be satisfied mostly by internal heat exchanges

Experimental characterization and modeling of an ethanol steam reformer

DEFF Research Database (Denmark)

Mandø, Matthias; Bovo, Mirko; Nielsen, Mads Pagh

2006-01-01

This work describes the characterization of an ethanol reforming system for a high temperature PEM fuel cell system. High temperature PEM fuel cells are well suited for operation on reformate gas due to the superior CO tolerance compared with low temperature PEM. Steam reforming of liquid biofuels...

Steam reforming of light oxygenates

DEFF Research Database (Denmark)

Trane-Restrup, Rasmus; Resasco, Daniel E; Jensen, Anker Degn

2013-01-01

Steam reforming (SR) of ethanol, acetic acid, acetone, acetol, 1-propanol, and propanal has been investigated over Ni/MgAl2O4 at temperatures between 400 and 700 degrees C and at a steam-to-carbon-ratio (S/C) of 6. The yield of H-2 and conversion increased with temperature, while the yield of by-...... of CH4. Significant deactivation of the catalyst was observed for all of the compounds and was mainly due to carbon formation. The carbon formation was highest for alcohols due to a high formation of olefins, which are potent coke precursors....

Bio-oil steam reforming, partial oxidation or oxidative steam reforming coupled with bio-oil dry reforming to eliminate CO{sub 2} emission

Energy Technology Data Exchange (ETDEWEB)

Hu, Xun [State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Graduate School of Chinese Academy of Sciences, Beijing 100039 (China); Lu, Gongxuan [State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000 (China)

2010-07-15

Biomass is carbon-neutral and utilization of biomass as hydrogen resource shows no impact on atmospheric CO{sub 2} level. Nevertheless, a significant amount of CO{sub 2} is always produced in biomass gasification processes. If the CO{sub 2} produced can further react with biomass, then the biomass gasification coupled with CO{sub 2} reforming of biomass will result in a net decrease of CO{sub 2} level in atmosphere and produce the chemical raw material, syngas. To achieve this concept, a ''Y'' type reactor is developed and applied in bio-oil steam reforming, partial oxidation, or oxidative steam reforming coupled with CO{sub 2} reforming of bio-oil to eliminate the emission of CO{sub 2}. The experimental results show that the reaction systems can efficiently suppress the emission of CO{sub 2} from various reforming processes. The different coupled reaction systems generate the syngas with different molar ratio of CO/H{sub 2}. In addition, coke deposition is encountered in the different reforming processes. Both catalysts and experimental parameters significantly affect the coke deposition. Ni/La{sub 2}O{sub 3} catalyst shows much higher resistivity toward coke deposition than Ni/Al{sub 2}O{sub 3} catalyst, while employing high reaction temperature is vital for elimination of coke deposition. Although the different coupled reaction systems show different characteristic in terms of product distribution and coke deposition, which all can serve as methods for storage of the carbon from fossil fuels or air. (author)

Stabilization of Savannah River National Laboratory (SRNL) Aqueous Waste by Fluidized Bed Steam Reforming (FBSR)

International Nuclear Information System (INIS)

Jantzen, C

2004-01-01

The Savannah River National Laboratory (SRNL) is a multidisciplinary laboratory operated by Westinghouse Savannah River Company (WSRC) in Aiken, South Carolina. Research and development programs have been conducted at SRNL for ∼50 years generating non-radioactive (hazardous and non-hazardous) and radioactive aqueous wastes. Typically the aqueous effluents from the R and D activities are disposed of from each laboratory module via the High Activity Drains (HAD) or the Low Activity Drains (LAD) depending on whether they are radioactive or not. The aqueous effluents are collected in holding tanks, analyzed and shipped to either H-Area (HAD waste) or the F/H Area Effluent Treatment Facility (ETF) (LAD waste) for volume reduction. Because collection, analysis, and transport of LAD and HAD waste is cumbersome and since future treatment of this waste may be curtailed as the F/H-Area evaporators and waste tanks are decommissioned, SRNL laboratory operations requested several proof of principle demonstrations of alternate technologies that would define an alternative disposal path for the aqueous wastes. Proof of principle for the disposal of SRNL HAD waste using a technology known as Fluidized Bed Steam Reforming (FBSR) is the focus of the current study. The FBSR technology can be performed either as a batch process, e.g. in each laboratory module in small furnaces with an 8'' by 8'' footprint, or in a semi-continuous Bench Scale Reformer (BSR). The proof of principle experiments described in this study cover the use of the FBSR technology at any scale (pilot or full scale). The proof of principle experiments described in this study used a non-radioactive HAD simulant

Fabrication and characteristics of cube-post microreactors for methanol steam reforming

International Nuclear Information System (INIS)

Zeng, Dehuai; Pan, Minqiang; Wang, Liming; Tang, Yong

2012-01-01

Highlights: ► We developed a cube-post microreactor for methanol steam reforming. ► We investigated the influences of micro-milling parameters on the burr formation during fabricating the cube posts. ► Larger cutting speed, smaller feed rate and cutting depth are in favor of obtaining relatively small burrs. ► Cube post and manifold structure show important effects on reaction performances at relatively low reaction temperature. -- Abstract: The lamination-plate structure patterned with microchannels and triangle manifolds regarded as one of the preferred constructions for micro fuel reformers. Learned from the microchannel plate structure, a similar plate structure with cube-post array and triangle manifolds is proposed in this work. A micro-milling process is applied to fabricate the cube posts on the plate surface, and the influences of cutting parameters on the burr formation are analyzed. Experimental results indicate that larger cutting speed, smaller feed rate and cutting depth are in favor of obtaining relatively small burrs. Two plates with different cube-post dimensions and manifold structures are experimentally investigated the performances of methanol steam reforming over the Cu/Zn/Al/Zr catalyst. It indicates that the reactor with small-scale cube posts and acute triangle manifold presents better reforming performances at 260 °C than that of the one with large-scale cube posts and right triangle manifolds. However, their performances are closed to each other at relatively high reaction temperature since the catalyst activity is situated in dominated position at the time.

Catalytic Steam Reforming of Bio-Oil to Hydrogen Rich Gas

DEFF Research Database (Denmark)

Trane-Restrup, Rasmus

heating value and high content of oxygen, which makes it unsuited for direct utilization in engines. One prospective technology for upgrading of bio-oil is steam reforming (SR), which can be used to produce H2 for upgrading of bio-oil through hydrodeoxygenation or synthesis gas for processes like......-oil. There are two main pathways to minimize carbon deposition in steam reforming; either through optimization of catalyst formulation or through changes to the process parameters, like changes in temperature, steam to carbon ratio (S/C), or adding O2 or H2 to the feed. In this thesis both pathways have been...

Methane steam reforming kinetics over Ni-YSZ anodematerials for Solid Oxide FuelCells

DEFF Research Database (Denmark)

Mogensen, David

of internal reforming has to be carefully controlled. The objective of this thesis is to make such a careful control possible by examining the rate of internal steam reforming in SOFCs. The catalytic steam reforming activity of Ni-YSZ anode material was tested both in a packed bed reactor to determine...

Thermoelectric generation coupling methanol steam reforming characteristic in microreactor

International Nuclear Information System (INIS)

Wang, Feng; Cao, Yiding; Wang, Guoqiang

2015-01-01

Thermoelectric (TE) generator converts heat to electric energy by thermoelectric material. However, heat removal on the cold side of the generator represents a serious challenge. To address this problem and for improved energy conversion, a thermoelectric generation process coupled with methanol steam reforming (SR) for hydrogen production is designed and analyzed in this paper. Experimental study on the cold spot character in a micro-reactor with monolayer catalyst bed is first carried out to understand the endothermic nature of the reforming as the thermoelectric cold side. A novel methanol steam reforming micro-reactor heated by waste heat or methanol catalytic combustion for hydrogen production coupled with a thermoelectric generation module is then simulated. Results show that the cold spot effect exists in the catalyst bed under all conditions, and the associated temperature difference first increases and then decreases with the inlet temperature. In the micro-reactor, the temperature difference between the reforming and heating channel outlets decreases rapidly with an increase in thermoelectric material's conductivity coefficient. However, methanol conversion at the reforming outlet is mainly affected by the reactor inlet temperature; while at the combustion outlet, it is mainly affected by the reactor inlet velocity. Due to the strong endothermic effect of the methanol steam reforming, heat supply of both kinds cannot balance the heat needed at reactor local areas, resulting in the cold spot at the reactor inlet. When the temperature difference between the thermoelectric module's hot and cold sides is 22 K, the generator can achieve an output voltage of 55 mV. The corresponding molar fraction of hydrogen can reach about 62.6%, which corresponds to methanol conversion rate of 72.6%. - Highlights: • Cold spot character of methanol steam reforming was studied through experiment. • Thermoelectric generation Coupling MSR process has been

An afterburner-powered methane/steam reformer for a solid oxide fuel cells application

Science.gov (United States)

Mozdzierz, Marcin; Chalusiak, Maciej; Kimijima, Shinji; Szmyd, Janusz S.; Brus, Grzegorz

2018-04-01

Solid oxide fuel cell (SOFC) systems can be fueled by natural gas when the reforming reaction is conducted in a stack. Due to its maturity and safety, indirect internal reforming is usually used. A strong endothermic methane/steam reforming process needs a large amount of heat, and it is convenient to provide thermal energy by burning the remainders of fuel from a cell. In this work, the mathematical model of afterburner-powered methane/steam reformer is proposed. To analyze the effect of a fuel composition on SOFC performance, the zero-dimensional model of a fuel cell connected with a reformer is formulated. It is shown that the highest efficiency of a solid oxide fuel cell is achieved when the steam-to-methane ratio at the reforming reactor inlet is high.

Task 19 - Sampling, Analysis, and Vitrification Study for Thermochem's Steam Reformer Treatment Technology

International Nuclear Information System (INIS)

Lillemoen, C.M.; McCollor, D.P.; Qi Sun

1998-01-01

The overall objective of the project is to provide support to Thermochem, Inc., in the demonstration of the steam reformer treatment technology to treat LLMW. Within this program, specific objectives include the following: (1) Analyze cerium, chlorine, and fluorine concentrations in samples from the pilot-scale steam reformer tests to determine partitioning of these elements, mass balances, and changes in concentration with time. (2) Perform experimental characterization of temperature--viscosity profiles to aid in determining vitrification viability for long-term stabilization. Additionally, calculations of viscosity will be performed for several blend combinations to complement the experimentally determined values. (3) Conduct leachability tests on the vitrified slags to aid in determining if product leachability falls within EPA guidelines and to assess the suitability of the vitrified material for long-term disposal

Fluidized Bed Steam Reforming of INEEL SBW Using THORsm Mineralizing Technology

Energy Technology Data Exchange (ETDEWEB)

Arlin L. Olson; Nicholas R. Soelberg; Douglas W. Marshall; Gary L. Anderson

2004-12-01

Sodium bearing waste (SBW) disposition is one of the U.S. Department of Energy (DOE) Idaho Operation Office’s (NE-ID) and State of Idaho’s top priorities at the Idaho National Engineering and Environmental Laboratory (INEEL). Many studies have resulted in the identification of five treatment alternatives that form a short list of perhaps the most appropriate technologies for the DOE to select from. The alternatives are (a) calcination with maximum achievable control technology (MACT) upgrade, (b) steam reforming, (c) cesium ion exchange (CsIX) with immobilization, (d) direct evaporation, and (e) vitrification. Each alternative has undergone some degree of applied technical development and preliminary process design over the past four years. DOE desired further experimental data, with regard to steam reforming technology, to make informed decisions concerning selection of treatment technology for SBW. Mineralizing steam reforming technology, offered by THOR Treatment Technologies, LLC would produce a denitrated, granular mineral waste form using a high-temperature fluidized bed process. A pilot scale demonstration of the technology was performed in a 15-cm-diameter reactor vessel September 27 through October 1, 2004. The pilot scale equipment is owned by the DOE, and located at the Science and Technology Applications Research (STAR) Center in Idaho Falls, ID. Flowsheet chemistry and operational parameters were defined through a collaborative effort involving Idaho National Engineering and Environmental Laboratory, Savannah River National Laboratory (SRNL), and THOR Treatment Technologies personnel. Personnel from Science Applications International Corporation, owners of the STAR Center, operated the pilot plant. The pilot scale test was terminated as planned after achieving a total of 100 hrs of cumulative/continuous processing operation. About 230 kg of SBW surrogate were processed that resulted in about 88 kg of solid product, a mass reduction of about 62

Analysis on Operating Parameter Design to Steam Methane Reforming in Heat Application RDE

Science.gov (United States)

Dibyo, Sukmanto; Sunaryo, Geni Rina; Bakhri, Syaiful; Zuhair; Irianto, Ign. Djoko

2018-02-01

The high temperature reactor has been developed with various power capacities and can produce electricity and heat application. One of heat application is used for hydrogen production. Most hydrogen production occurs by steam reforming that operated at high temperature. This study aims to analyze the feasibility of heat application design of RDE reactor in the steam methane reforming for hydrogen production using the ChemCAD software. The outlet temperature of cogeneration heat exchanger is analyzed to be applied as a feed of steam reformer. Furthermore, the additional heater and calculating amount of fuel usage are described. Results show that at a low mass flow rate of feed, its can produce a temperature up to 480°C. To achieve the temperature of steam methane reforming of 850°C the additional fired heater was required. By the fired heater, an amount of fuel usage is required depending on the Reformer feed temperature produced from the heat exchanger of the cogeneration system.

Hydrogen production from biomass pyrolysis gas via high temperature steam reforming process

International Nuclear Information System (INIS)

Wongchang, Thawatchai; Patumsawad, Suthum

2010-01-01

Full text: The aim of this work has been undertaken as part of the design of continuous hydrogen production using the high temperature steam reforming process. The steady-state test condition was carried out using syngas from biomass pyrolysis, whilst operating at high temperatures between 600 and 1200 degree Celsius. The main reformer operating parameters (e.g. temperature, resident time and steam to biomass ratio (S/B)) have been examined in order to optimize the performance of the reformer. The operating temperature is a key factor in determining the extent to which hydrogen production is increased at higher temperatures (900 -1200 degree Celsius) whilst maintaining the same as resident time and S/B ratio. The effects of exhaust gas composition on heating value were also investigated. The steam reforming process produced methane (CH 4 ) and ethylene (C 2 H 4 ) between 600 to 800 degree Celsius and enhanced production ethane (C 2 H 6 ) at 700 degree Celsius. However carbon monoxide (CO) emission was slightly increased for higher temperatures all conditions. The results show that the use of biomass pyrolysis gas can produce higher hydrogen production from high temperature steam reforming. In addition the increasing reformer efficiency needs to be optimized for different operating conditions. (author)

Development of a coupled reactor with a catalytic combustor and steam reformer for a 5 kW solid oxide fuel cell system

International Nuclear Information System (INIS)

Kang, Sanggyu; Lee, Kanghun; Yu, Sangseok; Lee, Sang Min; Ahn, Kook-Young

2014-01-01

Highlights: • Proposes the scale-up strategy to develop a large-scale coupled reactor. • Investigation of performance of steam reformer coupled with catalytic combustor. • Experimental parameters are inlet temp., air excess ratio, SCR, fuel utilization. • Evaluation of the heat transfer distribution along the gas flow direction. • The mean value of methane conversion rate is approximately 93.4%. - Abstract: The methane (CH 4 ) conversion rate of a steam reformer can be increased by thermal integration with a catalytic combustor, called a coupled reactor. In the present study, a 5 kW coupled reactor has been developed based on a 1 kW coupled reactor in previous work. The geometric parameters of the space velocity, diameter and length of the coupled reactor selected from the 1 kW coupled reactor are tuned and applied to the design of the 5 kW coupled reactor. To confirm the scale-up strategy, the performance of 5 kW coupled reactor is experimentally investigated with variations of operating parameters such as the fuel utilization in the solid oxide fuel cell (SOFC) stack, the inlet temperature of the catalytic combustor, the excess air ratio of the catalytic combustor, and the steam to carbon ratio (SCR) in the steam reformer. The temperature distributions of coupled reactors are measured along the gas flow direction. The gas composition at the steam reformer outlet is measured to find the CH 4 conversion rate of the coupled reactor. The maximum value of the CH 4 conversion rate is approximately 93.4%, which means the proposed scale-up strategy can be utilized to develop a large-scale coupled reactor

Hydrogen production by steam reforming methanol for polymer electrolyte fuel cells

International Nuclear Information System (INIS)

Amphlett, J.C.; Creber, K.A.M.; Davis, J.M.; Mann, R.F.; Peppley, B.A.; Stokes, D.M.

1993-01-01

Catalytic steam reforming of methanol has been studied as a means of generating hydrogen for a polymer electrolyte membrane fuel cell. A semi-empirical model of the kinetics of the catalytic steam reforming of methanol over Cu O/Zn O/Al 2 O 3 catalyst has been developed. This model is able to predict the performance of the reformer with respect to the various parameters important in developing an integrated reformer-polymer fuel cell system. A set of sample calculations of reformer temperature and CO production are given. The impact of the performance of the reformer catalyst on the design of the overall fuel cell power system is discussed. The selectivity of the catalyst to minimize CO content in the fuel gas is shown to be more critical than was previously believed. 4 figs., 4 tabs., 11 refs

Steam Reforming of Acetic Acid over Co-Supported Catalysts: Coupling Ketonization for Greater Stability

Energy Technology Data Exchange (ETDEWEB)

Davidson, Stephen D. [Energy and Environmental; Spies, Kurt A. [Energy and Environmental; Mei, Donghai [Energy and Environmental; Kovarik, Libor [Energy and Environmental; Kutnyakov, Igor [Energy and Environmental; Li, Xiaohong S. [Energy and Environmental; Lebarbier Dagle, Vanessa [Energy and Environmental; Albrecht, Karl O. [Energy and Environmental; Dagle, Robert A. [Energy and Environmental

2017-09-11

We report on the markedly improved stability of a novel 2-bed catalytic system, as compared to a conventional 1-bed steam reforming catalyst, for the production of H2 from acetic acid. The 2-bed catalytic system comprises of i) a basic oxide ketonization catalyst for the conversion of acetic acid to acetone, and a ii) Co-based steam reforming catalyst, both catalytic beds placed in sequence within the same unit operation. Steam reforming catalysts are particularly prone to catalytic deactivation when steam reforming acetic acid, used here as a model compound for the aqueous fraction of bio-oil. Catalysts comprising MgAl2O4, ZnO, CeO2, and activated carbon (AC) both with and without Co-addition were evaluated for conversion of acetic acid and acetone, its ketonization product, in the presence of steam. It was found that over the bare oxide support only ketonization activity was observed and coke deposition was minimal. With addition of Co to the oxide support steam reforming activity was facilitated and coke deposition was significantly increased. Acetone steam reforming over the same Co-supported catalysts demonstrated more stable performance and with less coke deposition than with acetic acid feedstock. DFT analysis suggests that over Co surface CHxCOO species are more favorably formed from acetic acid versus acetone. These CHxCOO species are strongly bound to the Co catalyst surface and could explain the higher propensity for coke formation from acetic acid. Based on these findings, in order to enhance stability of the steam reforming catalyst a dual-bed (2-bed) catalyst system was implemented. Comparing the 2-bed and 1-bed (Co-supported catalyst only) systems under otherwise identical reaction conditions the 2-bed demonstrated significantly improved stability and coke deposition was decreased by a factor of 4.

Methane steam reforming kinetics over Ni-YSZ anode materials for Solid Oxide Fuel Cells

DEFF Research Database (Denmark)

Mogensen, David

of internal reforming has to be carefully controlled. The objective of this thesis is to make such a careful control possible by examining the rate of internal steam reforming in SOFCs. The catalytic steam reforming activity of Ni-YSZ anode material was tested both in a packed bed reactor to determine...

Dynamic simulation of a furnace of steam reforming of natural gas

International Nuclear Information System (INIS)

Acuna, A; Fuentes, C; Smith, C A

1999-01-01

Steam reforming of natural gas is a very important industrial process in refineries and ammonia and methanol plants. Hydrogen is produced by reforming methane with steam. This hydrogen is essential in the hydro-treating process in the refineries thus, it is important to supervise and control the performance of the hydrogen plant. Mathematical models of refineries and chemical plants are used to simulate the behavior of the process units. However, the models especially of reactors like reformers are not very reliable. This paper presents a dynamic model of a furnace-reactor. The simulation results are validated with industrial data

Modeling and simulation of an isothermal reactor for methanol steam reforming

Directory of Open Access Journals (Sweden)

Raphael Menechini Neto

2014-04-01

Full Text Available Due to growing electricity demand, cheap renewable energy sources are needed. Fuel cells are an interesting alternative for generating electricity since they use hydrogen as their main fuel and release only water and heat to the environment. Although fuel cells show great flexibility in size and operating temperature (some models even operate at low temperatures, the technology has the drawback for hydrogen transportation and storage. However, hydrogen may be produced from methanol steam reforming obtained from renewable sources such as biomass. The use of methanol as raw material in hydrogen production process by steam reforming is highly interesting owing to the fact that alcohol has the best hydrogen carbon-1 ratio (4:1 and may be processed at low temperatures and atmospheric pressures. They are features which are desirable for its use in autonomous fuel cells. Current research develops a mathematical model of an isothermal methanol steam reforming reactor and validates it against experimental data from the literature. The mathematical model was solved numerically by MATLAB® and the comparison of its predictions for different experimental conditions indicated that the developed model and the methodology for its numerical solution were adequate. Further, a preliminary analysis was undertaken on methanol steam reforming reactor project for autonomous fuel cell.

Developing an energy efficient steam reforming process to produce hydrogen from sulfur-containing fuels

Science.gov (United States)

Simson, Amanda

Hydrogen powered fuel cells have the potential to produce electricity with higher efficiency and lower emissions than conventional combustion technology. In order to realize the benefits of a hydrogen fuel cell an efficient method to produce hydrogen is needed. Currently, over 90% of hydrogen is produced from the steam reforming of natural gas. However, for many applications including fuel cell vehicles, the use of a liquid fuel rather than natural gas is desirable. This work investigates the feasibility of producing hydrogen efficiently by steam reforming E85 (85% ethanol/15% gasoline), a commercially available sulfur-containing transportation fuel. A Rh-Pt/SiO2-ZrO2 catalyst has demonstrated good activity for the E85 steam reforming reaction. An industrial steam reforming process is often run less efficiently, with more water and at higher temperatures, in order to prevent catalyst deactivation. Therefore, it is desirable to develop a process that can operate without catalyst deactivation at more energy efficient conditions. In this study, the steam reforming of a sulfur-containing fuel (E85) was studied at near stoichiometric steam/carbon ratios and at 650C, conditions at which catalyst deactivation is normally measured. At these conditions the catalyst was found to be stable steam reforming a sulfur-free E85. However, the addition of low concentrations of sulfur significantly deactivated the catalyst. The presence of sulfur in the fuel caused catalyst deactivation by promoting ethylene which generates surface carbon species (coke) that mask catalytic sites. The amount of coke increased during time on stream and became increasingly graphitic. However, the deactivation due to both sulfur adsorption and coke formation was reversible with air treatment at 650°C. However, regenerations were found to reduce the catalyst life. Air regenerations produce exotherms on the catalyst surface that cause structural changes to the catalyst. During regenerations the

Steam Reforming Technology for Denitration and Immobilization of DOE Tank Wastes

International Nuclear Information System (INIS)

Mason, J. B.; McKibbin, J.; Ryan, K.; Schmoker, D.

2003-01-01

THOR Treatment Technologies, LLC (THOR) is a joint venture formed in June 2002 by Studsvik, Inc. (Studsvik) and Westinghouse Government Environmental Services Company LLC to further develop, market, and deploy Studsvik's patented THORSM non-incineration, steam reforming waste treatment technology. This paper provides an overview of the THORSM steam reforming process as applied to the denitration and conversion of Department of Energy (DOE) tank wastes to an immobilized mineral form. Using the THORSM steam reforming technology to treat nitrate containing tank wastes could significantly benefit the DOE by reducing capital and life-cycle costs, reducing processing and programmatic risks, and positioning the DOE to meet or exceed its stakeholder commitments for tank closure. Specifically, use of the THORSM technology can facilitate processing of up to 75% of tank wastes without the use of vitrification, yielding substantial life-cycle cost savings

Effect of microchannel structure on the reaction performance of methanol steam reforming

International Nuclear Information System (INIS)

Pan, Minqiang; Wu, Qiuyu; Jiang, Lianbo; Zeng, Dehuai

2015-01-01

Highlights: • Effect of microchannel cross-section and distribution on MSR are investigated. • Microchannel distribution shows much more influence on reaction performance. • SLDR and ELR with rectangular cross-section present better reaction performance. • DLSR and EUU with tooth cross-section have better reaction performance. • Equal-distribution of microchannels present the best reaction performance. - Abstract: Methanol steam reforming inside microchannel reactors is regarded as one of effective methods for supplying hydrogen for fuel cells. Microchannel structure plays an important role on the reaction performance of methanol steam reforming. Parallel and uniform-distributed microchannels with rectangular cross-section are generally adopted. In this work, two kinds of microchannel cross-sections and four kinds of microchannel distributions are selected to investigate the effect of microchannel structure on the reaction performance of methanol steam reforming. The result indicates that microchannel distribution shows much more influences on the reaction performance of methanol steam reforming than the microchannel cross-section. Sparse-distribution in the Left direction and Dense-distribution in the Right direction (SLDR) as well as Equal-distribution in the Left–Right direction (ELR) with rectangular cross-section present relatively good reaction performances, whereas Dense-distribution in the Left direction and Sparse-distribution in the Right direction (DLSR) as well as Equal-distribution in the Upside–Underside direction (EUU) with tooth cross-section have relatively good performances. ELR presents the best reaction performances of methanol steam reforming among all the investigated microchannel structures, whether rectangular or tooth cross-section

Reforming of natural gas—hydrogen generation for small scale stationary fuel cell systems

Science.gov (United States)

Heinzel, A.; Vogel, B.; Hübner, P.

The reforming of natural gas to produce hydrogen for fuel cells is described, including the basic concepts (steam reforming or autothermal reforming) and the mechanisms of the chemical reactions. Experimental work has been done with a compact steam reformer, and a prototype of an experimental reactor for autothermal reforming was tested, both containing a Pt-catalyst on metallic substrate. Experimental results on the steam reforming system and a comparison of the steam reforming process with the autothermal process are given.

Syngas Production from CO2 Reforming and CO2-steam Reforming of Methane over Ni/Ce-SBA-15 Catalyst

Science.gov (United States)

Tan, J. S.; Danh, H. T.; Singh, S.; Truong, Q. D.; Setiabudi, H. D.; Vo, D.-V. N.

2017-06-01

This study compares the catalytic performance of mesoporous 10 Ni/Ce-SBA-15 catalyst for CO2 reforming and CO2-steam reforming of methane reactions in syngas production. The catalytic performance of 10 Ni/Ce-SBA-15 catalyst for CO2 reforming and CO2-steam reforming of methane was evaluated in a temperature-controlled tubular fixed-bed reactor at stoichiometric feed composition, 1023 K and atmospheric pressure for 12 h on-stream with gas hourly space velocity (GHSV) of 36 L gcat -1 h-1. The 10 Ni/Ce-SBA-15 catalyst possessed a high specific BET surface area and average pore volume of 595.04 m2 g-1. The XRD measurement revealed the presence of NiO phase with crystallite dimension of about 13.60 nm whilst H2-TPR result indicates that NiO phase was completely reduced to metallic Ni0 phase at temperature beyond 800 K and the reduction temperature relied on different degrees of metal-support interaction associated with the location and size of NiO particles. The catalytic reactivity was significantly enhanced with increasing H2O/CO2 feed ratio. Interestingly, the H2/CO ratio for CO2-steam reforming of methane varied between 1 and 3 indicated the occurrence of parallel reactions, i.e., CH4 steam reforming giving a H2/CO of 3 whilst reverse water-gas shift (RWGS) reaction consuming H2 to produce CO gaseous product.

Modeling, Simulation and Optimization of Hydrogen Production Process from Glycerol using Steam Reforming

International Nuclear Information System (INIS)

Park, Jeongpil; Cho, Sunghyun; Kim, Tae-Ok; Shin, Dongil; Lee, Seunghwan; Moon, Dong Ju

2014-01-01

For improved sustainability of the biorefinery industry, biorefinery-byproduct glycerol is being investigated as an alternate source for hydrogen production. This research designs and optimizes a hydrogen-production process for small hydrogen stations using steam reforming of purified glycerol as the main reaction, replacing existing processes relying on steam methane reforming. Modeling, simulation and optimization using a commercial process simulator are performed for the proposed hydrogen production process from glycerol. The mixture of glycerol and steam are used for making syngas in the reforming process. Then hydrogen are produced from carbon monoxide and steam through the water-gas shift reaction. Finally, hydrogen is separated from carbon dioxide using PSA. This study shows higher yield than former U.S.. DOE and Linde studies. Economic evaluations are performed for optimal planning of constructing domestic hydrogen energy infrastructure based on the proposed glycerol-based hydrogen station

Catalytic glycerol steam reforming for hydrogen production

International Nuclear Information System (INIS)

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

2015-01-01

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 H 2 . In this work we present the results obtained in the process of steam reforming of glycerol on Ni/Al 2 O 3 . The catalyst was prepared by wet impregnation method and characterized through different methods: N 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 2 , CH 4 , CO, CO 2 . The optimum reaction conditions as resulted from this study are: temperature 550°C, Gly:H 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%

Numerical analysis of performance of steam reformer of methane reforming hydrogen production system connected with high-temperature gas-cooled reactor

International Nuclear Information System (INIS)

Yin Huaqiang; Jiang Shengyao; Zhang Youjie

2007-01-01

Methane conversion rate and hydrogen output are important performance indexes of the steam reformer. The paper presents numerical analysis of performance of the reformer connected with high-temperature gas-cooled reactor HTR-10. Setting helium inlet flow rate fixed, performance of the reformer was examined with different helium inlet temperature, pressure, different process gas temperature, pressure, flow rate, and different steam to carbon ratio. As the range concerned, helium inlet temperature has remarkable influence on the performance, and helium inlet temperature, process gas temperature and pressure have little influence on the performance, and improving process gas flow rate, methane conversion rate decreases and hydrogen output increases, however improving steam to carbon ratio has reverse influence on the performance. (authors)

Preliminary assessment of synthesis gas production via hybrid steam reforming of methane and glycerol

NARCIS (Netherlands)

Balegedde Ramachandran, P.; van Rossum, G.; Kersten, Sascha R.A.; van Swaaij, Willibrordus Petrus Maria

2012-01-01

In this article, hybrid steam reforming (HSR) of desulphurized methane, together with crude glycerol, in existing commercial steam reformers to produce synthesis gas is proposed. The proposed concept consists of a gasifier to produce vapors, gases, and char from crude glycerol, which is coupled with

Steam reforming of low-level mixed waste. Final report

Energy Technology Data Exchange (ETDEWEB)

NONE

1998-06-01

ThermoChem has successfully designed, fabricated and operated a nominal 90 pound per hour Process Development Unit (PDU) on various low-level mixed waste surrogates. The design, construction, and testing of the PDU as well as performance and economic projections for a 300-lb/hr demonstration and commercial system are described. The overall system offers an environmentally safe, non-incinerating, cost-effective, and publicly acceptable method of processing LLMW. The steam-reforming technology was ranked the No. 1 non-incineration technology for destruction of hazardous organic wastes in a study commissioned by the Mixed Waste Focus Area and published in April 1997. The ThermoChem steam-reforming system has been developed over the last 13 years culminating in this successful test campaign on LLMW surrogates. Six surrogates were successfully tested including a 750-hour test on material simulating a PCB- and Uranium-contaminated solid waste found at the Portsmouth Gaseous Diffusion Plant. The test results indicated essentially total (> 99.9999%) destruction of RCRA and TSCA hazardous halogenated organics, significant levels of volume reduction (> 400 to 1), and retention of radionuclides in the volume-reduced solids. Economic evaluations have shown the steam-reforming system to be very cost competitive with more conventional and other emerging technologies.

Steam reforming of low-level mixed waste. Final report

International Nuclear Information System (INIS)

1998-06-01

ThermoChem has successfully designed, fabricated and operated a nominal 90 pound per hour Process Development Unit (PDU) on various low-level mixed waste surrogates. The design, construction, and testing of the PDU as well as performance and economic projections for a 300-lb/hr demonstration and commercial system are described. The overall system offers an environmentally safe, non-incinerating, cost-effective, and publicly acceptable method of processing LLMW. The steam-reforming technology was ranked the No. 1 non-incineration technology for destruction of hazardous organic wastes in a study commissioned by the Mixed Waste Focus Area and published in April 1997. The ThermoChem steam-reforming system has been developed over the last 13 years culminating in this successful test campaign on LLMW surrogates. Six surrogates were successfully tested including a 750-hour test on material simulating a PCB- and Uranium-contaminated solid waste found at the Portsmouth Gaseous Diffusion Plant. The test results indicated essentially total (> 99.9999%) destruction of RCRA and TSCA hazardous halogenated organics, significant levels of volume reduction (> 400 to 1), and retention of radionuclides in the volume-reduced solids. Economic evaluations have shown the steam-reforming system to be very cost competitive with more conventional and other emerging technologies

Ethanol internal steam reforming in intermediate temperature solid oxide fuel cell

Science.gov (United States)

Diethelm, Stefan; Van herle, Jan

This study investigates the performance of a standard Ni-YSZ anode supported cell under ethanol steam reforming operating conditions. Therefore, the fuel cell was directly operated with a steam/ethanol mixture (3 to 1 molar). Other gas mixtures were also used for comparison to check the conversion of ethanol and of reformate gases (H 2, CO) in the fuel cell. The electrochemical properties of the fuel cell fed with four different fuel compositions were characterized between 710 and 860 °C by I- V and EIS measurements at OCV and under polarization. In order to elucidate the limiting processes, impedance spectra obtained with different gas compositions were compared using the derivative of the real part of the impedance with respect of the natural logarithm of the frequency. Results show that internal steam reforming of ethanol takes place significantly on Ni-YSZ anode only above 760 °C. Comparisons of results obtained with reformate gas showed that the electrochemical cell performance is dominated by the conversion of hydrogen. The conversion of CO also occurs either directly or indirectly through the water-gas shift reaction but has a significant impact on the electrochemical performance only above 760 °C.

Preliminary design of steam reformer in out-pile demonstration test facility for HTTR heat utilization system

Energy Technology Data Exchange (ETDEWEB)

Haga, Katsuhiro; Hino, Ryutaro; Inagaki, Yosiyuki; Hata, Kazuhiko; Aita, Hideki; Sekita, Kenji; Nishihara, Tetsuo; Sudo, Yukio [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment; Yamada, Seiya

1996-11-01

One of the key objectives of HTTR is to demonstrate effectiveness of high-temperature nuclear heat utilization system. Prior to connecting a heat utilization system to HTTR, an out-pile demonstration test is indispensable for the development of experimental apparatuses, operational control and safety technology, and verification of the analysis code of safety assessment. For the first heat utilization system of HTTR, design of the hydrogen production system by steam reforming is going on. We have proposed the out-pile demonstration test plan of the heat utilization system and conducted preliminary design of the test facility. In this report, design of the steam reformer, which is the principal component of the test facility, is described. In the course of the design, two types of reformers are considered. The one reformer contains three reactor tubes and the other contains one reactor tube to reduce the construction cost of the test facility. We have selected the steam reformer operational conditions and structural specifications by analyzing the steam reforming characteristics and component structural strength for each type of reformer. (author)

BENCH SCALE SALTSTONE PROCESS DEVELOPMENT MIXING STUDY

Energy Technology Data Exchange (ETDEWEB)

Cozzi, A.; Hansen, E.

2011-08-03

The Savannah River National Laboratory (SRNL) was requested to develop a bench scale test facility, using a mixer, transfer pump, and transfer line to determine the impact of conveying the grout through the transfer lines to the vault on grout properties. Bench scale testing focused on the effect the transfer line has on the rheological property of the grout as it was processed through the transfer line. Rheological and other physical properties of grout samples were obtained prior to and after pumping through a transfer line. The Bench Scale Mixing Rig (BSMR) consisted of two mixing tanks, grout feed tank, transfer pump and transfer hose. The mixing tanks were used to batch the grout which was then transferred into the grout feed tank. The contents of the feed tank were then pumped through the transfer line (hose) using a progressive cavity pump. The grout flow rate and pump discharge pressure were monitored. Four sampling stations were located along the length of the transfer line at the 5, 105 and 205 feet past the transfer pump and at 305 feet, the discharge of the hose. Scaling between the full scale piping at Saltstone to bench scale testing at SRNL was performed by maintaining the same shear rate and total shear at the wall of the transfer line. The results of scaling down resulted in a shorter transfer line, a lower average velocity, the same transfer time and similar pressure drops. The condition of flow in the bench scale transfer line is laminar. The flow in the full scale pipe is in the transition region, but is more laminar than turbulent. The resulting plug in laminar flow in the bench scale results in a region of no-mixing. Hence mixing, or shearing, at the bench scale should be less than that observed in the full scale, where this plug is non existent due to the turbulent flow. The bench scale tests should be considered to be conservative due to the highly laminar condition of flow that exists. Two BSMR runs were performed. In both cases, wall

Steam reforming and oxidative steam reforming of methanol over CuO-CeO{sub 2} catalysts

Energy Technology Data Exchange (ETDEWEB)

Udani, P.P.C.; Gunawardana, P.V.D.S.; Lee, Hyun Chan; Kim, Dong Hyun [Department of Chemical Engineering, Kyungpook National University, Daegu 702-701 (Korea)

2009-09-15

Steam reforming (SRM) and oxidative steam reforming of methanol (OSRM) were carried out over a series of coprecipitated CuO-CeO{sub 2} catalysts with varying copper content in the range of 30-80 at.% Cu (= 100 x Cu/(Cu + Ce)). The effects of copper content, reaction temperature and O{sub 2} concentration on catalytic activity were investigated. The activity of CuO-CeO{sub 2} catalysts for SRM and OSRM increased with the copper content and 70 at.% CuO-CeO{sub 2} catalyst showed the highest activity in the temperature range of 160-300 C for both SRM and OSRM. After SRM or OSRM, the copper species in the catalysts observed by XRD were mainly metallic copper with small amount of CuO and Cu{sub 2}O, an indication that metallic copper is an active species in the catalysis of both SRM and OSRM. It was observed that the methanol conversion increased considerably with the addition of O{sub 2} into the feed stream, indicating that the partial oxidation of methanol (POM) is much faster than SRM. The optimum 70 at.% CuO-CeO{sub 2} catalyst showed stable activities for both SRM and OSRM reactions at 300 C. (author)

Optimizing the Heat Exchanger Network of a Steam Reforming System

DEFF Research Database (Denmark)

Nielsen, Mads Pagh; Korsgaard, Anders Risum; Kær, Søren Knudsen

2004-01-01

Proton Exchange Membrane (PEM) based combined heat and power production systems are highly integrated energy systems. They may include a hydrogen production system and fuel cell stacks along with post combustion units optionally coupled with gas turbines. The considered system is based on a natural...... stationary numerical system model was used and process integration techniques for optimizing the heat exchanger network for the reforming unit are proposed. Objective is to minimize the system cost. Keywords: Fuel cells; Steam Reforming; Heat Exchanger Network (HEN) Synthesis; MINLP....... gas steam reformer along with gas purification reactors to generate clean hydrogen suited for a PEM stack. The temperatures in the various reactors in the fuel processing system vary from around 1000°C to the stack temperature at 80°C. Furthermore, external heating must be supplied to the endothermic...

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%.

Steam reforming of bio-oil from coconut shell pyrolysis over Fe/olivine catalyst

International Nuclear Information System (INIS)

Quan, Cui; Xu, Shaoping; Zhou, Congcong

2017-01-01

Highlights: • Steam reforming of the actual bio-oil was investigated with Fe/olivine catalyst. • Most of phenols in bio-oil were converted into gas products. • A carbon conversion of 97.2% was obtained under optimized conditions. - Abstract: Catalytic steam reforming of coconut shell pyrolysis bio-oil over Fe/olivine catalyst was conducted in a fixed-bed quartz reactor. The effects of calcination temperature, iron loading, reaction temperature, steam to carbon ratio (S/C), bio-oil weight hourly space velocity (W b HSV) on gas composition and carbon conversion were investigated. The results indicate that Fe/olivine has good activity for steam reforming of bio-oil, the couple Fe 2+/3+ /Fe 2+ may be sufficiently efficient for C–C, C–O and C–H breaking. After steam reforming, most of the phenolics in pyrolysis oil are converted into light molecular compounds such as H 2 , CO, CO 2 , and CH 4 . The H 2 concentration and carbon conversion were enhanced by increasing reaction temperature from 750 to 800 °C and the S/C from 1.5 to 2, but decreased with increasing calcination temperature. In the W b HSV range of 0.5–0.6, the hydrogen concentration decreased obviously, whereas it decreased slightly by further increasing W b HSV. The highest hydrogen concentration of 47.6 vol% was obtained among the catalysts tested, and the best carbon conversion was 97.2% over 10% Fe/olivine catalyst under the reforming conditions of temperature = 800 °C, W b HSV = 0.5, S/C = 2.

Hydrogen yield from low temperature steam reforming of ethanol

Energy Technology Data Exchange (ETDEWEB)

Das, N.K.; Dalai, A.K. [Saskatchewan Univ., Saskatoon, SK (Canada). Dept. of Chemical Engineering, Catalysis and Chemical Reaction Engineering Laboratories; Ranganathan, R. [Saskatchewan Research Council, Saskatoon, SK (Canada)

2007-02-15

Interest in the use of ethanol for fuel cell hydrogen production was discussed with particular reference to a study in which the production of hydrogen was maximized through low temperature steam reforming of ethanol in the temperature range of 200 to 360 degrees C. The primary objective of this study was to determine the effect of Mn concentration on a Cu/Al{sub 2}O{sub 3} catalyst for steam reforming of ethanol to produce hydrogen. The purpose was to maximize ethanol conversion and hydrogen selectivity in the lowest possible reaction temperature for the ideal catalyst activity. The optimum reaction conditions in the presence of a suitable catalyst can produce the desired products of hydrogen and carbon dioxide. Cu/Al{sub 2}O{sub 3} catalysts with six different concentrations ranging from 0 to 10 weight per cent Mn, were prepared, characterized and studied for the ethanol-steam reforming reaction. The effects of different process variables were studied, including water-to-ethanol feed ratio, space time and catalyst reduction temperatures on ethanol conversion and hydrogen yield. Maximum ethanol conversion of 60.7 per cent and hydrogen yield of 3.74 (mol of hydrogen per mol of ethanol converted) were observed at 360 degrees C for a catalyst with 2.5 weight per cent Mn loading. 29 refs., 3 tabs., 12 figs.

Development and test evaluation of duplex steam reformer tube

International Nuclear Information System (INIS)

Allen, D.C.; Meyer, D.J.; Pflasterer, G.R.

1980-01-01

For HTR applications involving a steam reformer (SR), it is uncertain whether an intermediate heat exchanger (IHX) is required. There are several system configurations that could be developed for the application of nuclear heat using the steam reformer reaction. The considerations (advantages vs. disadvantages) for each of the system configurations are summarized. The approach that technically and economically appears to be the most attractive, in studies conducted by General Electric, combines the SR process heat exchanger and the IHX in a single component using a duplex tube. A central question concerning the duplex tube concept is whether the design would provide adequate leak monitoring capability and significant reduction in tritium and hydrogen diffusion, while introducing only a small increase in overall temperature difference from the helium to the process gas. A cooperative GE-KFA effort was undertaken to develop, fabricate, test, and evaluate a duplex steam reformer tube. GE was responsible for the development and fabrication of the tube, and KFA was responsible for testing the tube in the EVA I facility at Juelich. Both GE and KFA are evaluating the thermochemical and metallurgical test data. Actual fabrication of the tube was performed by Foster-Wheeler in accordance with the GE design. This paper reviews the highlights of the fabrication development and preliminary evaluation of the test data

Out-of-pile demonstration test of HTTR hydrogen production system structure and fabrication technology of steam reformer. Contract research

International Nuclear Information System (INIS)

Inagaki, Yoshiyuki; Ouchi, Yoshihiro; Fujisaki, Katsuo; Kato, Michio; Uno, Hisao; Hayashi, Koji; Aita, Hideki

1999-10-01

A hydrogen production system by steam reforming of natural gas, chemical reaction; CH 4 +H 2 O = 3H 2 +CO, is to be the first heat utilization system of the HTTR. Prior to coupling of the steam reforming system with the HTTR, an out-of-pile test facility is presently under construction in order to confirm safety, controllability and performance of the steam reforming system under simulated operational conditions of the HTTR hydrogen production system. The out-of-pile test facility, using an electric heater as a reactor substitute, simulates key components downstream an intermediate heat exchanger of the HTTR hydrogen production system on a scale of 1 to 30 with a hydrogen production rate of 110 Nm 3 /h. A steam reformer (SR) is a key component to produce hydrogen by steam reforming of natural gas. A bayonet-type catalyst tube was applied to the SR of the out-of-pile test facility in order to enhance the heat utilization rate. Also to promote heat transfer, the thickness of the catalyst tube should be decreased to 10 mm while augmenting heat transfer by fins formed on the outer surface of the catalyst tube. Therefore, the catalyst tube was designed on the basis of pressure difference between helium and process gases instead of total pressure of them. This design method was authorized for the first time in Japan. Furthermore, a function of explosion proof was applied to the SR because it contains inflammable gas and electric heater. This report describes the structure of the SR as well as the authorization both of the design method of the catalyst tube and the explosion proof function of the SR. (author)

Fluidized bed steam reformed mineral waste form performance testing to support Hanford Supplemental Low Activity Waste Immobilization Technology Selection

Energy Technology Data Exchange (ETDEWEB)

Jantzen, C. M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Pierce, E. M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bannochie, C. J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Burket, P. R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Cozzi, A. D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Crawford, C. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Daniel, W. E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Fox, K. M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Herman, C. C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Miller, D. H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Missimer, D. M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Nash, C. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Williams, M. F. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Brown, C. F. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, N. P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Neeway, J. J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Valenta, M. M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Gill, G. A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Swanberg, D. J. [Washington River Protection Solutions (WRPS), Richland, WA (United States); Robbins, R. A. [Washington River Protection Solutions (WRPS), Richland, WA (United States); Thompson, L. E. [Washington River Protection Solutions (WRPS), Richland, WA (United States)

2015-10-01

This report describes the benchscale testing with simulant and radioactive Hanford Tank Blends, mineral product characterization and testing, and monolith testing and characterization. These projects were funded by DOE EM-31 Technology Development & Deployment (TDD) Program Technical Task Plan WP-5.2.1-2010-001 and are entitled “Fluidized Bed Steam Reformer Low-Level Waste Form Qualification”, Inter-Entity Work Order (IEWO) M0SRV00054 with Washington River Protection Solutions (WRPS) entitled “Fluidized Bed Steam Reforming Treatability Studies Using Savannah River Site (SRS) Low Activity Waste and Hanford Low Activity Waste Tank Samples”, and IEWO M0SRV00080, “Fluidized Bed Steam Reforming Waste Form Qualification Testing Using SRS Low Activity Waste and Hanford Low Activity Waste Tank Samples”. This was a multi-organizational program that included Savannah River National Laboratory (SRNL), THOR® Treatment Technologies (TTT), Pacific Northwest National Laboratory (PNNL), Oak Ridge National Laboratory (ORNL), Office of River Protection (ORP), and Washington River Protection Solutions (WRPS). The SRNL testing of the non-radioactive pilot-scale Fluidized Bed Steam Reformer (FBSR) products made by TTT, subsequent SRNL monolith formulation and testing and studies of these products, and SRNL Waste Treatment Plant Secondary Waste (WTP-SW) radioactive campaign were funded by DOE Advanced Remediation Technologies (ART) Phase 2 Project in connection with a Work-For-Others (WFO) between SRNL and TTT.

Thermal analysis of cylindrical natural-gas steam reformer for 5 kW PEMFC

Science.gov (United States)

Jo, Taehyun; Han, Junhee; Koo, Bonchan; Lee, Dohyung

2016-11-01

The thermal characteristics of a natural-gas based cylindrical steam reformer coupled with a combustor are investigated for the use with a 5 kW polymer electrolyte membrane fuel cell. A reactor unit equipped with nickel-based catalysts was designed to activate the steam reforming reaction without the inclusion of high-temperature shift and low-temperature shift processes. Reactor temperature distribution and its overall thermal efficiency depend on various inlet conditions such as the equivalence ratio, the steam to carbon ratio (SCR), and the fuel distribution ratio (FDR) into the reactor and the combustor components. These experiments attempted to analyze the reformer's thermal and chemical properties through quantitative evaluation of product composition and heat exchange between the combustor and the reactor. FDR is critical factor in determining the overall performance as unbalanced fuel injection into the reactor and the combustor deteriorates overall thermal efficiency. Local temperature distribution also influences greatly on the fuel conversion rate and thermal efficiency. For the experiments, the operation conditions were set as SCR was in range of 2.5-4.0 and FDR was in 0.4-0.7 along with equivalence ratio of 0.9-1.1; optimum results were observed for FDR of 0.63 and SCR of 3.0 in the cylindrical steam reformer.

Synthesis gas production via hybrid steam reforming of natural gas and bio-liquids

OpenAIRE

Balegedde Ramachandran, P.

2013-01-01

This thesis deals with (catalytic) steam reforming of bio-liquids for the production of synthesis gas. Glycerol, both crude from the biodiesel manufacturing and refined, and pyrolysis oil are tested as bio-based feedstocks. Liquid bio-based feeds could be preferred over inhomogeneous fibrous solid biomass because of their logistic advantages, better mineral balance, and better processability. Especially the ease of pressurization, which is required for large scale synthesis gas production, is...

Out-of-pile demonstration test of HTTR hydrogen production system structure and fabrication technology of steam reformer. Contract research

Energy Technology Data Exchange (ETDEWEB)

Inagaki, Yoshiyuki; Ouchi, Yoshihiro; Fujisaki, Katsuo; Kato, Michio; Uno, Hisao; Hayashi, Koji; Aita, Hideki [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment

1999-10-01

A hydrogen production system by steam reforming of natural gas, chemical reaction; CH{sub 4}+H{sub 2}O = 3H{sub 2}+CO, is to be the first heat utilization system of the HTTR. Prior to coupling of the steam reforming system with the HTTR, an out-of-pile test facility is presently under construction in order to confirm safety, controllability and performance of the steam reforming system under simulated operational conditions of the HTTR hydrogen production system. The out-of-pile test facility, using an electric heater as a reactor substitute, simulates key components downstream an intermediate heat exchanger of the HTTR hydrogen production system on a scale of 1 to 30 with a hydrogen production rate of 110 Nm{sup 3}/h. A steam reformer (SR) is a key component to produce hydrogen by steam reforming of natural gas. A bayonet-type catalyst tube was applied to the SR of the out-of-pile test facility in order to enhance the heat utilization rate. Also to promote heat transfer, the thickness of the catalyst tube should be decreased to 10 mm while augmenting heat transfer by fins formed on the outer surface of the catalyst tube. Therefore, the catalyst tube was designed on the basis of pressure difference between helium and process gases instead of total pressure of them. This design method was authorized for the first time in Japan. Furthermore, a function of explosion proof was applied to the SR because it contains inflammable gas and electric heater. This report describes the structure of the SR as well as the authorization both of the design method of the catalyst tube and the explosion proof function of the SR. (author)

Hydrogen production via catalytic steam reforming of fast pyrolysis oil fractions

International Nuclear Information System (INIS)

Wang, D.; Czernik, S.; Montane, D.; Mann, M.; Chornet, E.

1997-01-01

Hydrogen is the prototype of the environmentally cleanest fuel of interest for power generation using fuel cells, and as a co-adjuvant or autonomous transportation fuel in internal combustion engines. The conversion of biomass to hydrogen can be carried out through two distinct thermochemical strategies: (a) gasification followed by shift conversion; (b) catalytic steam reforming and shift conversion of specific fractions derived from fast pyrolysis and aqueous/steam processes of biomass. This paper shows that fast pyrolysis of biomass results in a bio-oil that can be adequately fractionated into valuable co-products leaving as by-product an aqueous fraction containing soluble organics (a mixture of alcohols, aldehydes and acids). This fraction can be converted to hydrogen by catalytic steam reforming followed by a shift conversion step. The methods used, the yields obtained and their economic significance will be discussed. (author)

Design of a steam reforming system to be connected to the HTTR

International Nuclear Information System (INIS)

Hada, K.; Nishihara, T.; Shibata, T.; Shiozawa, S.

1996-01-01

Top priority objective for developing the first heat utilization system to be connected to the HTTR is to demonstrate technical feasibility of a nuclear process heat utilization system for production of hydrogen for the first time in the world. Major issues to be resolved for coupling the heat utilization system to the HTTR are 1)to develop safety philosophy for reasonably and reliably ensuring safety of the nuclear reactor, 2)to develop control design concept for the total system of the nuclear reactor and heat utilization system because thermal dynamics of endothermic chemical reactor to be heated by nuclear heat is much different from the nuclear reactor, 3)to develop helium-heated components and 4)to develop enhanced hydrogen production technologies for achieving competitiveness to a fossil-fired plant. A steam reforming hydrogen production system was studied as one of the first priority candidates for an HTTR-heat utilization system due to matured technology in fossil-fired plants and since technical solutions demonstrated by the coupling of the steam reforming system to the HTTR will contribute to all other hydrogen production systems. Basic design philosophy for the HTTR-steam reforming system is that the steam reforming plant downstream of an intermediate secondary helium loop is designed at the same safety level as fossil-fired plants and therefore the secondary helium loop was selected as a safety barrier to the HTTR nuclear reactor. (J.P.N.)

Optimizing a steam-methane reformer for hydrogen production

NARCIS (Netherlands)

de Jong, M.; Reinders, Angelina H.M.E.; Kok, Jacobus B.W.; Westendorp, G.

2009-01-01

By means of steam reforming, natural gas is converted to carbon dioxide and hydrogen. The reactions take place in reactor tubes which are covered with catalyst at the inside, where the reactive mixture flows. At the outside they are heated by combustion of natural gas with air. In this paper the

Fluidized Bed Steam Reforming of Hanford LAW Using THORsm Mineralizing Technology

International Nuclear Information System (INIS)

Olson, Arlin L.; Nicholas R Soelberg; Douglas W. Marshall; Gary L. Anderson

2004-01-01

The U.S. Department of Energy (DOE) documented, in 2002, a plan for accelerating cleanup of the Hanford Site, located in southeastern Washington State, by at least 35 years. A key element of the plan was acceleration of the tank waste program and completion of tank waste treatment by 2028 by increasing the capacity of the planned Waste Treatment Plant (WTP) and using supplemental technologies for waste treatment and immobilization. The plan identified steam reforming technology as a candidate for supplemental treatment of as much as 70% of the low-activity waste (LAW). Mineralizing steam reforming technology, offered by THOR Treatment Technologies, LLC would produce a denitrated, granular mineral waste form using a high-temperature fluidized bed process. A pilot scale demonstration of the technology was completed in a 15-cm-diameter reactor vessel. The pilot scale facility was equipped with a highly efficient cyclone separator and heated sintered metal filters for particulate removal, a thermal oxidizer for reduced gas species and NOx destruction, and a packed activated carbon bed for residual volatile species capture. The pilot scale equipment is owned by the DOE, but located at the Science and Technology Applications Research (STAR) Center in Idaho Falls, ID. Pilot scale testing was performed August 2-5, 2004. Flowsheet chemistry and operational parameters were defined through a collaborative effort involving Idaho National Engineering and Environmental Laboratory, Savannah River National Laboratory (SRNL), and THOR Treatment Technologies personnel. Science Application International Corporation, owners of the STAR Center, personnel performed actual pilot scale operation. The pilot scale test achieved a total of 68.7 hrs of cumulative/continuous processing operation before termination in response to a bed de-fluidization condition. 178 kg of LAW surrogate were processed that resulted in 148 kg of solid product, a mass reduction of about 17%. The process achieved

Fluidized Bed Steam Reforming of Hanford LAW Using THORsm Mineralizing Technology

Energy Technology Data Exchange (ETDEWEB)

Olson, Arlin L.; Nicholas R Soelberg; Douglas W. Marshall; Gary L. Anderson

2004-11-01

The U.S. Department of Energy (DOE) documented, in 2002, a plan for accelerating cleanup of the Hanford Site, located in southeastern Washington State, by at least 35 years. A key element of the plan was acceleration of the tank waste program and completion of ''tank waste treatment by 2028 by increasing the capacity of the planned Waste Treatment Plant (WTP) and using supplemental technologies for waste treatment and immobilization.'' The plan identified steam reforming technology as a candidate for supplemental treatment of as much as 70% of the low-activity waste (LAW). Mineralizing steam reforming technology, offered by THOR Treatment Technologies, LLC would produce a denitrated, granular mineral waste form using a high-temperature fluidized bed process. A pilot scale demonstration of the technology was completed in a 15-cm-diameter reactor vessel. The pilot scale facility was equipped with a highly efficient cyclone separator and heated sintered metal filters for particulate removal, a thermal oxidizer for reduced gas species and NOx destruction, and a packed activated carbon bed for residual volatile species capture. The pilot scale equipment is owned by the DOE, but located at the Science and Technology Applications Research (STAR) Center in Idaho Falls, ID. Pilot scale testing was performed August 2–5, 2004. Flowsheet chemistry and operational parameters were defined through a collaborative effort involving Idaho National Engineering and Environmental Laboratory, Savannah River National Laboratory (SRNL), and THOR Treatment Technologies personnel. Science Application International Corporation, owners of the STAR Center, personnel performed actual pilot scale operation. The pilot scale test achieved a total of 68.7 hrs of cumulative/continuous processing operation before termination in response to a bed de-fluidization condition. 178 kg of LAW surrogate were processed that resulted in 148 kg of solid product, a mass reduction of about 17%. The process

Application of flexible micro temperature sensor in oxidative steam reforming by a methanol micro reformer.

Science.gov (United States)

Lee, Chi-Yuan; Lee, Shuo-Jen; Shen, Chia-Chieh; Yeh, Chuin-Tih; Chang, Chi-Chung; Lo, Yi-Man

2011-01-01

Advances in fuel cell applications reflect the ability of reformers to produce hydrogen. This work presents a flexible micro temperature sensor that is fabricated based on micro-electro-mechanical systems (MEMS) technology and integrated into a flat micro methanol reformer to observe the conditions inside that reformer. The micro temperature sensor has higher accuracy and sensitivity than a conventionally adopted thermocouple. Despite various micro temperature sensor applications, integrated micro reformers are still relatively new. This work proposes a novel method for integrating micro methanol reformers and micro temperature sensors, subsequently increasing the methanol conversion rate and the hydrogen production rate by varying the fuel supply rate and the water/methanol ratio. Importantly, the proposed micro temperature sensor adequately controls the interior temperature during oxidative steam reforming of methanol (OSRM), with the relevant parameters optimized as well.

Application of Flexible Micro Temperature Sensor in Oxidative Steam Reforming by a Methanol Micro Reformer

Directory of Open Access Journals (Sweden)

Yi-Man Lo

2011-02-01

Full Text Available Advances in fuel cell applications reflect the ability of reformers to produce hydrogen. This work presents a flexible micro temperature sensor that is fabricated based on micro-electro-mechanical systems (MEMS technology and integrated into a flat micro methanol reformer to observe the conditions inside that reformer. The micro temperature sensor has higher accuracy and sensitivity than a conventionally adopted thermocouple. Despite various micro temperature sensor applications, integrated micro reformers are still relatively new. This work proposes a novel method for integrating micro methanol reformers and micro temperature sensors, subsequently increasing the methanol conversion rate and the hydrogen production rate by varying the fuel supply rate and the water/methanol ratio. Importantly, the proposed micro temperature sensor adequately controls the interior temperature during oxidative steam reforming of methanol (OSRM, with the relevant parameters optimized as well.

Characterization of steam-reforming catalysts

Directory of Open Access Journals (Sweden)

Santos D. C. R.M.

2004-01-01

Full Text Available The effect of the addition of Mg and Ca to Ni/ a-Al2O3 catalysts was investigatedstudied, aiming to detail the promotion mechanismaddress their role as promoters in the steam reforming reaction. Temperature- programmed reduction and H2 and CO temperature-programmed desorption experiments indicated that Mg interacts with the metallic phase. Mg-promoted catalysts showed a greater difficulty for Ni precursors reduction besides different probe molecules (H2 and CO adsorbed states. In the conversion of cyclohexane, Mg inhibited the formation of hydrogenolysis products. Nonetheless, the presence of Ca did not influence the metallic phase.

Staged catalytic gasification/steam reforming of pyrolysis oil

NARCIS (Netherlands)

van Rossum, G.; Kersten, Sascha R.A.; van Swaaij, Willibrordus Petrus Maria

2009-01-01

Gasification/steam reforming of pyrolysis oil was studied in a staged reactor concept, which consisted of an inert fluidized bed and a catalytic fixed bed. Methane and C2−C3 free syngas is produced at a single temperature around 800 °C at atmospheric pressure. By lowering the temperature of the

Density functional theory study of acetic acid steam reforming on Ni(111)

Science.gov (United States)

Ran, Yan-Xiong; Du, Zhen-Yi; Guo, Yun-Peng; Feng, Jie; Li, Wen-Ying

2017-04-01

Catalytic steam reforming of bio-oil is a promising process to convert biomass into hydrogen. To shed light on this process, acetic acid is selected as the model compound of the oxygenates in bio-oil, and density functional theory is applied to investigate the mechanism of acetic acid steam reforming on the Ni(111) surface. The most favorable pathway of this process on the Ni(111) surface is suggested as CH3COOH* → CH3COO* → CH3CO* → CH2CO* → CH2* + CO* → CH* → CHOH* → CHO* → CO*, followed by the water gas shift reaction to produce CO2 and H2. CH* species are identified as the major carbon deposition precursor, and the water gas shift reaction is the rate-determining step during the whole acetic acid steam reforming process, as CO* + OH* → cis-COOH* is kinetically restricted with the highest barrier of 1.85 eV. Furthermore, the formation pathways and initial dissociation of important intermediates acetone and acetaldehyde are also investigated.

Design of the steam reformer for the HTR-10 high temperature process heat application

International Nuclear Information System (INIS)

Ju Huaiming; Xu Yuanhui; Jia Haijun

2000-01-01

The 10 MW High Temperature Reactor Test Module (HTR-10) is being constructed now and planned to be operational in 2000. One of the objectives is to develop the high temperature process heat application. The methane steam reformer is one of the key-facilities for the nuclear process heat application system. The paper describes the conceptual design of the HTR-10 Steam Reformer with He heating, and the design optimization computer code. It can be used to perform sensitivity analysis for parameters, and to improve the design. Principal parameters and construction features of the HTR-10 reformer heated by He are introduced. (author)

PdZnAl Catalysts for the Reactions of Water-Gas-Shift, Methanol Steam Reforming, and Reverse-Water-Gas-Shift

Energy Technology Data Exchange (ETDEWEB)

Dagle, Robert A.; Platon, Alexandru; Datye, Abhaya K.; Vohs, John M.; Wang, Yong; Palo, Daniel R.

2008-03-07

Pd/ZnO/Al2O3 catalysts were studied for water-gas-shift (WGS), methanol steam reforming, and reverse-water-gas-shift (RWGS) reactions. WGS activity was found to be dependent on the Pd:Zn ratio with a maximum activity obtained at approximately 0.50, which was comparable to that of a commercial Pt-based catalyst. The catalyst stability was demonstrated for 100 hours time-on-stream at a temperature of 3600C without evidence of metal sintering. WGS reaction rates were approximately 1st order with respect to CO concentration, and kinetic parameters were determined to be Ea = 58.3 kJ mol-1 and k0 = 6.1x107 min-1. During methanol steam reforming, the CO selectivities were observed to be lower than the calculated equilibrium values over a range of temperatures and steam/carbon ratios studied while the reaction rate constants were approximately of the same magnitude for both WGS and methanol steam reforming. These results indicate that although Pd/ZnO/Al2O3 are active WGS catalysts, WGS is not involved in methanol steam reforming. RWGS rate constants are on the order of about 20 times lower than that of methanol steam reforming, suggesting that RWGS reaction could be one of the sources for small amount of CO formation in methanol steam reforming.

Low Temperature Steam Methane Reforming Over Ni Based Catalytic Membrane Prepared by Electroless Palladium Plating.

Science.gov (United States)

Lee, Sang Moon; Hong, Sung Chang; Kim, Sung Su

2018-09-01

A Pd/Ni-YSZ porous membrane with different palladium loadings and hydrazine as a reducing reagent was prepared by electroless plating and evaluated for the steam methane reforming activity. The steam-reforming activity of a Ni-YSZ porous membrane was greatly increased by the deposition of 4 g/L palladium in the low-temperature range (600 °C). With an increasing amount of reducing reagent, the Pd clusters were well dispersed on the Ni-YSZ surface and were uniform in size (∼500 nm). The Pd/Ni-YSZ catalytic porous membrane prepared by 1 of Pd/hydrazine ratio possessed an abundant amount of metallic Pd. The optimal palladium loadings and Pd/hydrazine ratio increased the catalytic activity in both the steam-reforming reaction and the Pd dispersion.

Thermodynamic evaluation of hydrogen production for fuel cells by using bio-ethanol steam reforming: Effect of carrier gas addition

Science.gov (United States)

Hernández, Liliana; Kafarov, Viatcheslav

Omitting the influence of the addition of carrier gas to the reaction system for hydrogen production by bio-ethanol steam reforming can lead to wrong conclusions, especially when it is going to be made to scale. The effect of carrier gas addition to produce hydrogen using bio-ethanol steam reforming to feed fuel cells was evaluated. Thermodynamic calculations in equilibrium conditions were made, however the analysis derived from them can also be applied to kinetic conditions. These calculations were made by using the Aspen-HYSYS software at atmospheric pressure and different values of temperature, water/ethanol molar ratios, and inert (argon)/(water/ethanol) molar ratios. The addition of inert carrier gas modifies the concentrations of the reaction products in comparison to those obtained without its presence. This behavior occurs because most of the reactions which take place in bio-ethanol steam reforming have a positive difference of moles. This fact enhances the system sensitivity to inert concentration at low and moderated temperatures (<700 °C). At high values of temperature, the inert addition does not influence the composition of the reaction products because of the predominant effect of inverse WGS reaction.

Thermodynamic evaluation of hydrogen production for fuel cells by using bio-ethanol steam reforming: Effect of carrier gas addition

Energy Technology Data Exchange (ETDEWEB)

Hernandez, Liliana; Kafarov, Viatcheslav [Universidad Industrial de Santander, Escuela de Ingenieria Quimica, Bucaramanga 678 (Colombia)

2009-07-01

Omitting the influence of the addition of carrier gas to the reaction system for hydrogen production by bio-ethanol steam reforming can lead to wrong conclusions, especially when it is going to be made to scale. The effect of carrier gas addition to produce hydrogen using bio-ethanol steam reforming to feed fuel cells was evaluated. Thermodynamic calculations in equilibrium conditions were made, however the analysis derived from them can also be applied to kinetic conditions. These calculations were made by using the Aspen-HYSYS software at atmospheric pressure and different values of temperature, water/ethanol molar ratios, and inert (argon)/(water/ethanol) molar ratios. The addition of inert carrier gas modifies the concentrations of the reaction products in comparison to those obtained without its presence. This behavior occurs because most of the reactions which take place in bio-ethanol steam reforming have a positive difference of moles. This fact enhances the system sensitivity to inert concentration at low and moderated temperatures (<700 C). At high values of temperature, the inert addition does not influence the composition of the reaction products because of the predominant effect of inverse WGS reaction. (author)

Catalytic steam reforming of ethanol for hydrogen production: Brief status

Directory of Open Access Journals (Sweden)

Bineli Aulus R.R.

2016-01-01

Full Text Available Hydrogen represents a promising fuel since it is considered as a cleanest energy carrier and also because during its combustion only water is emitted. It can be produced from different kinds of renewable feedstocks, such as ethanol, in this sense hydrogen could be treated as biofuel. Three chemical reactions can be used to achieve this purpose: the steam reforming (SR, the partial oxidation (POX and the autothermal reforming (ATR. In this study, the catalysts implemented in steam reforming of ethanol were reviewed. A wide variety of elements can be used as catalysts for this reaction, such as base metals (Ni, Cu and Co or noble metals (Rh, Pt and Ru usually deposited on a support material that increases surface area and improves catalytic function. The use of Rh, Ni and Pt supported or promoted with CeO2, and/or La2O3 shows excellent performance in ethanol SR catalytic process. The ratio of water to ethanol, reaction temperatures, catalysts loadings, selectivity and activity are also discussed as they are extremely important for high hydrogen yields.

Duplex tube steam reformer development program

International Nuclear Information System (INIS)

Lewe, C.K.; Nieto, J.M.; Papadopoulos, A.

1978-09-01

Work done in partial fulfillment of Task 7 of the Duplex Steam Reformer Development Program is described. The DSR concept acts as a double barrier between a process heat high temperature reactor plant (PNP) and a closed loop chemical heat pipe (CHP) for the long distance transport of chemical energy to a remote industrial user. The current state of the DSR design is described as well as related systems and equipment. The PNP concept presented is based upon work currently underway in the Federal Republic of Germany

Thermodynamics of Hydrogen Production from Dimethyl Ether Steam Reforming and Hydrolysis

Energy Technology Data Exchange (ETDEWEB)

T.A. Semelsberger

2004-10-01

The thermodynamic analyses of producing a hydrogen-rich fuel-cell feed from the process of dimethyl ether (DME) steam reforming were investigated as a function of steam-to-carbon ratio (0-4), temperature (100 C-600 C), pressure (1-5 atm), and product species: acetylene, ethanol, methanol, ethylene, methyl-ethyl ether, formaldehyde, formic acid, acetone, n-propanol, ethane and isopropyl alcohol. Results of the thermodynamic processing of dimethyl ether with steam indicate the complete conversion of dimethyl ether to hydrogen, carbon monoxide and carbon dioxide for temperatures greater than 200 C and steam-to-carbon ratios greater than 1.25 at atmospheric pressure (P = 1 atm). Increasing the operating pressure was observed to shift the equilibrium toward the reactants; increasing the pressure from 1 atm to 5 atm decreased the conversion of dimethyl ether from 99.5% to 76.2%. The order of thermodynamically stable products in decreasing mole fraction was methane, ethane, isopropyl alcohol, acetone, n-propanol, ethylene, ethanol, methyl-ethyl ether and methanol--formaldehyde, formic acid, and acetylene were not observed. The optimal processing conditions for dimethyl ether steam reforming occurred at a steam-to-carbon ratio of 1.5, a pressure of 1 atm, and a temperature of 200 C. Modeling the thermodynamics of dimethyl ether hydrolysis (with methanol as the only product considered), the equilibrium conversion of dimethyl ether is limited. The equilibrium conversion was observed to increase with temperature and steam-to-carbon ratio, resulting in a maximum dimethyl ether conversion of approximately 68% at a steam-to-carbon ratio of 4.5 and a processing temperature of 600 C. Thermodynamically, dimethyl ether processed with steam can produce hydrogen-rich fuel-cell feeds--with hydrogen concentrations exceeding 70%. This substantiates dimethyl ether as a viable source of hydrogen for PEM fuel cells.

In silico search for novel methane steam reforming catalysts

DEFF Research Database (Denmark)

Xu, Yue; Lausche, Adam C; Wang, Shengguang

2013-01-01

App’) with a microkinetic modeling technique to predict the rates and selectivities of a prospective material. This paper illustrates this screening technique using the steam reforming of methane to carbon monoxide and hydrogen as a test reaction. While catalysts are already commercially available for this process...

Hydrogen production from biomass tar by catalytic steam reforming

International Nuclear Information System (INIS)

Yoon, Sang Jun; Choi, Young-Chan; Lee, Jae-Goo

2010-01-01

The catalytic steam reforming of model biomass tar, toluene being a major component, was performed at various conditions of temperature, steam injection rate, catalyst size, and space time. Two kinds of nickel-based commercial catalyst, the Katalco 46-3Q and the Katalco 46-6Q, were evaluated and compared with dolomite catalyst. Production of hydrogen generally increased with reaction temperature, steam injection rate and space time and decreased with catalyst size. In particular, zirconia-promoted nickel-based catalyst, Katalco 46-6Q, showed a higher tar conversion efficiency and shows 100% conversion even relatively lower temperature conditions of 600 deg. C. Apparent activation energy was estimated to 94 and 57 kJ/mol for dolomite and nickel-based catalyst respectively.

Thermodynamic evaluation of hydrogen production via bioethanol steam reforming

Energy Technology Data Exchange (ETDEWEB)

Tasnadi-Asztalos, Zsolt; Cormos, Ana-Maria; Imre-Lucaci, Árpád; Cormos, Călin C. [Babes-Bolyai University, Faculty of Chemistry and Chemical Engineering, Arany Janos 11, RO-400028, Cluj-Napoca (Romania)

2013-11-13

In this article, a thermodynamic analysis for bioethanol steam reforming for hydrogen production is presented. Bioethanol is a newly proposed renewable energy carrier mainly produced from biomass fermentation. Reforming of bioethanol provides a promising method for hydrogen production from renewable resources. Steam reforming of ethanol (SRE) takes place under the action of a metal catalyst capable of breaking C-C bonds into smaller molecules. A large domain for the water/bioethanol molar ratio as well as the temperature and average pressure has been used in the present work. The interval of investigated temperature was 100-800°C, the pressure was in the range of 1-10 bar and the molar ratio was between 3-25. The variations of gaseous species concentration e.g. H{sub 2}, CO, CO{sub 2}, CH{sub 4} were analyzed. The concentrations of the main products (H{sub 2} and CO) at lower temperature are smaller than the ones at higher temperature due to by-products formation (methane, carbon dioxide, acetylene etc.). The concentration of H2 obtained in the process using high molar ratio (>20) is higher than the one at small molar ratio (near stoichiometric). When the pressure is increased the hydrogen concentration decreases. The results were compared with literature data for validation purposes.

Towards H2-rich gas production from unmixed steam reforming of methane: Thermodynamic modeling

Science.gov (United States)

Lima da Silva, Aline; Müller, Iduvirges Lourdes

2011-10-01

In this work, the Gibbs energy minimization method is applied to investigate the unmixed steam reforming (USR) of methane to generate hydrogen for fuel cell application. The USR process is an advanced reforming technology that relies on the use of separate air and fuel/steam feeds to create a cyclic process. Under air flow (first half of the cycle), a bed of Ni-based material is oxidized, providing the heat necessary for the steam reforming that occurs subsequently during fuel/steam feed stage (second half of the cycle). In the presence of CaO sorbent, high purity hydrogen can be produced in a single reactor. In the first part of this work, it is demonstrated that thermodynamic predictions are consistent with experimental results from USR isothermal tests under fuel/steam feed. From this, it is also verified that the reacted NiO to CH4 (NiOreacted/CH4) molar ratio is a very important parameter that affects the product gas composition and decreases with time. At the end of fuel/steam flow, the reforming reaction is the most important chemical mechanism, with H2 production reaching ∼75 mol%. On the other hand, at the beginning of fuel/steam feed stage, NiO reduction reactions dominate the equilibrium system, resulting in high CO2 selectivity, negative steam conversion and low concentrations of H2. In the second part of this paper, the effect of NiOreacted/CH4 molar ratio on the product gas composition and enthalpy change during fuel flow is investigated at different temperatures for inlet H2O/CH4 molar ratios in the range of 1.2-4, considering the USR process operated with and without CaO sorbent. During fuel/steam feed stage, the energy demand increases as time passes, because endothermic reforming reaction becomes increasingly important as this stage nears its end. Thus, the duration of the second half of the cycle is limited by the conditions under which auto-thermal operation can be achieved. In absence of CaO, H2 at concentrations of approximately 73 mol% can

CATALYTIC STEAM REFORMING OF CHLOROCARBONS: METHLYCHLORIDE. (R822721C633)

Science.gov (United States)

The effective destruction of trichloroethane, trichloroethylene and perchloroethylene by steam reforming with a commercial nickel catalyst has been demonstrated. Conversion levels of up to 0.99999 were attained in both laboratory and semi-pilot experiments, with the products c...

Catalytic Steam Reforming of Toluene as a Model Compound of Biomass Gasification Tar Using Ni-CeO2/SBA-15 Catalysts

Directory of Open Access Journals (Sweden)

Erik Dahlquist

2013-07-01

Full Text Available Nickel supported on SBA-15 doped with CeO2 catalysts (Ni-CeO2/SBA-15 was prepared, and used for steam reforming of toluene which was selected as a model compound of biomass gasification tar. A fixed-bed lab-scale set was designed and employed to evaluate the catalytic performances of the Ni-CeO2/SBA-15 catalysts. Experiments were performed to reveal the effects of several factors on the toluene conversion and product gas composition, including the reaction temperature, steam/carbon (S/C ratio, and CeO2 loading content. Moreover, the catalysts were subjected to analysis of their carbon contents after the steam reforming experiments, as well as to test the catalytic stability over a long experimental period. The results indicated that the Ni-CeO2/SBA-15 catalysts exhibited promising capabilities on the toluene conversion, anti-coke deposition and catalytic stability. The toluene conversion reached as high as 98.9% at steam reforming temperature of 850 °C and S/C ratio of 3 using the Ni-CeO2(3wt%/SBA-15 catalyst. Negligible coke formation was detected on the used catalyst. The gaseous products mainly consisted of H2 and CO, together with a little CO2 and CH4.

Parametric study of hydrogen production from ethanol steam reforming in a membrane microreactor

Directory of Open Access Journals (Sweden)

M. de-Souza

2013-06-01

Full Text Available Microreactors are miniaturized chemical reaction systems, which contain reaction channels with characteristic dimensions in the range of 10-500 µm. One possible application for microreactors is the conversion of ethanol to hydrogen used in fuel cells to generate electricity. In this paper a rigorous isothermal, steady-state two-dimensional model was developed to simulate the behavior of a membrane microreactor based on the hydrogen yield from ethanol steam reforming. Furthermore, this membrane microreactor is compared to a membraneless microreactor. A potential advantage of the membrane microreactor is the fact that both ethanol steam reforming and the separation of hydrogen by a permselective membrane occur in one single microdevice. The simulation results for steam reforming yields are in agreement with experimental data found in the literature. The results show that the membrane microreactorpermits a hydrogen yield of up to 0.833 which is more than twice that generated by the membraneless reactor. More than 80% of the generated hydrogen permeates through the membrane and, due to its high selectivity, the membrane microreactor delivers high-purity hydrogen to the fuel cell.

Hydrogen generation from bioethanol reforming: bench-scale unit performance with Cu/Nb2O5 catalyst

International Nuclear Information System (INIS)

Fernandes Machado, N.R.C.; Schmal, M.; Cantao, M.P.

2003-01-01

As an alternative route for hydrogen production, ethanol reforming was studied in a bench-scale unit using a 5%Cu/Nb 2 O 5 catalyst previously selected in a micro reactor. X-Ray Diffraction analysis has shown that this catalyst contains copper oxide in an amorphous form, or in particles smaller than 20 nm, while the Nb 2 O 5 is highly crystalline. Analysis of the calcinated catalyst by X-Ray Photoelectron Spectroscopy revealed that 35% of total copper was on the surface as Cu I (55%) or Cu II (45%). The catalyst presented a low surface area (35 m 2 /g), mainly from meso and macropores, as textural analysis revealed. Temperature Programmed Reduction showed a two-step reduction of Cu II to Cu, at 245 o C and 306 o C. It was also observed the reduction of 6% of Nb 2 O 5 . The reaction unit consisted of an integral reactor with 16 g of catalyst pellets, approximately 3 mm x 5 mm in size. Reaction temperature and feed rate were varied to optimize hydrogen production, with CO 2 as the main byproduct. Reagents (water and ethanol) in stoichiometric proportion were fed into an electric pre-heater and vaporized. An increase on reaction temperature from 300 o C to 400 o C has led to an increase in mean conversion from 17% to 35%. Ethene and ethyl ether were also detected as minor byproducts. (author)

Hydrogen Production by Steam Reforming of Natural Gas Over Vanadium-Nickel-Alumina Catalysts.

Science.gov (United States)

Yoo, Jaekyeong; Park, Seungwon; Song, Ji Hwan; Song, In Kyu

2018-09-01

A series of vanadium-nickel-alumina (xVNA) catalysts were prepared by a single-step sol-gel method with a variation of vanadium content (x, wt%) for use in the hydrogen production by steam reforming of natural gas. The effect of vanadium content on the physicochemical properties and catalytic activities of xVNA catalysts in the steam reforming of natural gas was investigated. It was found that natural gas conversion and hydrogen yield showed volcano-shaped trends with respect to vanadium content. It was also revealed that natural gas conversion and hydrogen yield increased with decreasing nickel crystallite size.

Preparation and characterization of nickel catalysts supported on cerium for obtaining hydrogen from steam reforming of ethanol

International Nuclear Information System (INIS)

Urbaninho, A.B.; Bergamaschi, V.S.; Ferreira, J.C.

2016-01-01

The Ni/Ce catalysts for were prepared by co- precipitation method with a view to their use in steam reforming of ethanol to produce a hydrogen-rich gas mixture. The catalysts were characterized by scanning electron microscopy; x-ray dispersive Spectroscopy and surface area BET method. This paper proposes to prepare, characterize and test nickel catalyst supported on cerium in order to obtain a material with higher activity and selectivity of the catalyst using the steam reforming reaction of ethanol, by varying the reaction temperature, molar ratio water/ethanol and uptime. The catalytic tests were monitored by chemical analysis of syngas from steam reforming of ethanol using an analysis online by gas Chromatograph in the reactor. (author)

Synergetic mechanism of methanol–steam reforming reaction in a catalytic reactor with electric discharges

International Nuclear Information System (INIS)

Kim, Taegyu; Jo, Sungkwon; Song, Young-Hoon; Lee, Dae Hoon

2014-01-01

Highlights: • Methanol–steam reforming was performed on Cu catalysts under an electric discharge. • Discharge had a synergetic effect on the catalytic reaction for methanol conversion. • Discharge lowered the temperature for catalyst activation or light off. • Discharge controlled the yield and selectivity of species in a reforming process. • Adsorption triggered by a discharge was a possible mechanism for a synergetic effect. - Abstract: Methanol–steam reforming was performed on Cu/ZnO/Al 2 O 3 catalysts under an electric discharge. The discharge occurred between the electrodes where the catalysts were packed. The electric discharge was characterized by the discharge voltage and electric power to generate the discharge. The existence of a discharge had a synergetic effect on the catalytic reaction for methanol conversion. The electric discharge provided modified reaction paths resulting in a lower temperature for catalyst activation or light off. The discharge partially controlled the yield and selectivity of species in a reforming process. The aspect of control was examined in view of the reaction kinetics. The possible mechanisms for the synergetic effect between the catalytic reaction and electric discharge on methanol–steam reforming were addressed. A discrete reaction path, particularly adsorption triggered by an electric discharge, was suggested to be the most likely mechanism for the synergetic effect. These results are expected to provide a guide for understanding the plasma–catalyst hybrid reaction

Kinetic Study of Nonequilibrium Plasma-Assisted Methane Steam Reforming

Directory of Open Access Journals (Sweden)

Hongtao Zheng

2014-01-01

Full Text Available To develop a detailed reaction mechanism for plasma-assisted methane steam reforming, a comprehensive numerical and experimental study of effect laws on methane conversion and products yield is performed at different steam to methane molar ratio (S/C, residence time s, and reaction temperatures. A CHEMKIN-PRO software with sensitivity analysis module and path flux analysis module was used for simulations. A set of comparisons show that the developed reaction mechanism can accurately predict methane conversion and the trend of products yield in different operating conditions. Using the developed reaction mechanism in plasma-assisted kinetic model, the reaction path flux analysis was carried out. The result shows that CH3 recombination is the limiting reaction for CO production and O is the critical species for CO production. Adding 40 wt.% Ni/SiO2 in discharge region has significantly promoted the yield of H2, CO, or CO2 in dielectric packed bed (DPB reactor. Plasma catalytic hybrid reforming experiment verifies the reaction path flux analysis tentatively.

Data Quality Objectives For Selecting Waste Samples To Test The Fluid Bed Steam Reformer Test

International Nuclear Information System (INIS)

Banning, D.L.

2010-01-01

This document describes the data quality objectives to select archived samples located at the 222-S Laboratory for Fluid Bed Steam Reformer testing. The type, quantity and quality of the data required to select the samples for Fluid Bed Steam Reformer testing are discussed. In order to maximize the efficiency and minimize the time to treat Hanford tank waste in the Waste Treatment and Immobilization Plant, additional treatment processes may be required. One of the potential treatment processes is the fluid bed steam reformer (FBSR). A determination of the adequacy of the FBSR process to treat Hanford tank waste is required. The initial step in determining the adequacy of the FBSR process is to select archived waste samples from the 222-S Laboratory that will be used to test the FBSR process. Analyses of the selected samples will be required to confirm the samples meet the testing criteria.

2D heat and mass transfer modeling of methane steam reforming for hydrogen production in a compact reformer

International Nuclear Information System (INIS)

Ni Meng

2013-01-01

Highlights: ► A heat and mass transfer model is developed for a compact reformer. ► Hydrogen production from methane steam reforming is simulated. ► Increasing temperature greatly increases the reaction rates at the inlet. ► Temperature in the downstream is increased at higher rate of heat supply. ► Larger permeability enhances gas flow and reaction rates in the catalyst layer. - Abstract: Compact reformers (CRs) are promising devices for efficient fuel processing. In CRs, a thin solid plate is sandwiched between two catalyst layers to enable efficient heat transfer from combustion duct to the reforming duct for fuel processing. In this study, a 2D heat and mass transfer model is developed to investigate the fundamental transport phenomenon and chemical reaction kinetics in a CR for hydrogen production by methane steam reforming (MSR). Both MSR reaction and water gas shift reaction (WGSR) are considered in the numerical model. Parametric simulations are performed to examine the effects of various structural/operating parameters, such as pore size, permeability, gas velocity, temperature, and rate of heat supply on the reformer performance. It is found that the reaction rates of MSR and WGSR are the highest at the inlet but decrease significantly along the reformer. Increasing the operating temperature raises the reaction rates at the inlet but shows very small influence in the downstream. For comparison, increasing the rate of heat supply raises the reaction rates in the downstream due to increased temperature. A high gas velocity and permeability facilitates gas transport in the porous structure thus enhances reaction rates in the downstream of the reformer.

A numerical analysis of heat and mass transfer during the steam reforming process of ethane

Science.gov (United States)

Tomiczek, Marcin; Kaczmarczyk, Robert; Mozdzierz, Marcin; Brus, Grzegorz

2017-11-01

This paper presents a numerical analysis of heat and mass transfer during the steam reforming of ethane. From a chemical point of view, the reforming process of heavy hydrocarbons, such as ethane, is complex. One of the main issue is a set of undesired chemical reactions that causes the deposition of solid carbon and consequently blocks the catalytic property of a reactor. In the literature a carbon deposition regime is selected by thermodynamical analysis to design safe operation conditions. In the case of Computational Fluid Dynamic (CFD, hereafter) models each control volume should be investigated to determinate if carbon deposition is thermodynamically favourable. In this paper the authors combine equilibrium and kinetics analysis to simulate the steam reforming of methane-ethane rich fuel. The results of the computations were juxtaposed with experimental data for methane steam reforming, and good agreement was found. An analysis based on the kinetics of reactions was conducted to predict the influence of temperature drop and non-equilibrium composition on solid carbon deposition. It was found that strong non-uniform temperature distribution in the reactor causes conditions favourable for carbon deposition at the inlet of the reformer. It was shown that equilibrium calculations, often used in the literature, are insufficient.

Hydrogen production by ethanol steam reforming over co-hydrotalcites having basic sites

Energy Technology Data Exchange (ETDEWEB)

Contreras, J.L.; Salmones, J.; Garcia, L.A.; Ponce, A.; Zeifert, B.; Fuentes, G.A. [Univ. Autonoma Metropolitana-Azcapotzalco, Mexico City (Mexico); Contreras, J.L.; Salmones, J.; Garcia, L.A.; Ponce, A.; Zeifert, B.; Fuentes, G.A. [Inst. Politecnico Nacional, Mexico City (Mexico); Contreras, J.L.; Salmones, J.; Garcia, L.A.; Ponce, A.; Zeifert, B.; Fuentes, G.A. [Univ. Autonoma Metropolitana-Iztapalapa, Mexico City (Mexico)

2008-04-15

The catalytic steam reforming process can be used to produce hydrogen from ethanol for use in fuel cells. In comparison to methanol or gasoline, ethanol offers many advantages, notably, it is a renewable resource and neutral with respect to emissions of carbon dioxide (CO{sub 2}); it is less toxic; it can be readily stored without handling risk; and it can be obtained in large quantities from biomass. The reaction of ethanol with steam is strongly endothermic and can form undesirable products during the reaction. This article presented a study that combined, for the first time, the catalytic properties of cobalt (Co) with a new family of supports that are the hydrotalcites of high surface area and with basic sites. Co/Hydrotalcite catalysts were prepared, characterized and evaluated during the steam reforming of ethanol from 500 to 650 degrees Celsius. The article discussed the experiment, including the preparation of catalysts; characterization of solids; and catalytic evaluation. Scanning electron microscopy and x-ray diffraction studies were also described. Results were described in terms of area and pore volume distribution; thermogravimetric analysis and differential thermal analysis; temperature-programmed desorption (TPD) of CO{sub 2}; scanning electron microscopy; x-ray diffraction; the crystalline nature of cobalt; and ethanol steam-reforming reaction. It was concluded that the Co concentration was enriched on the hydrotalcite surface. In addition, a direct relationship between the Co concentration and the total basicity was found. A direct relationship between basicity and the conversion was also found. 27 refs., 3 tabs., 12 figs.

Sorption-enhanced steam methane reforming in fluidized bed reactors

Energy Technology Data Exchange (ETDEWEB)

Johnsen, Kim

2006-10-15

Hydrogen is considered to be an important potential energy carrier; however, its advantages are unlikely to be realized unless efficient means can be found to produce it without generation of CO{sub 2}. Sorption-enhanced steam methane reforming (SE-SMR) represent a novel, energy-efficient hydrogen production route with in situ CO{sub 2} capture, shifting the reforming and water gas shift reactions beyond their conventional thermodynamic limits. The use of fluidized bed reactors for SE-SMR has been investigated. Arctic dolomite, a calcium-based natural sorbent, was chosen as the primary CO{sub 2}-acceptor in this study due to high absorption capacity, relatively high reaction rate and low cost. An experimental investigation was conducted in a bubbling fluidized bed reactor of diameter 0.1 m, which was operated cyclically and batch wise, alternating between reforming/carbonation conditions and higher-temperature calcination conditions. Hydrogen concentrations of >98 mole% on a dry basis were reached at 600 C and 1 atm, for superficial gas velocities in the range of {approx}0.03-0.1 m/s. Multiple reforming-regeneration cycles showed that the hydrogen concentration remained at {approx}98 mole% after four cycles. The total production time was reduced with an increasing number of cycles due to loss of CO{sub 2}-uptake capacity of the dolomite, but the reaction rates of steam reforming and carbonation seemed to be unaffected for the conditions investigated. A modified shrinking core model was applied for deriving carbonation kinetics of Arctic dolomite, using experimental data from a novel thermo gravimetric reactor. An apparent activation energy of 32.6 kj/mole was found from parameter fitting, which is in good agreement with previous reported results. The derived rate expression was able to predict experimental conversion up to {approx}30% very well, whereas the prediction of higher conversion levels was poorer. However, the residence time of sorbent in a continuous

Steam reforming of ethanol over nickel-tungsten catalyst

Energy Technology Data Exchange (ETDEWEB)

Hernandez, I.P.; Fernandez, A.M. [Centro de Investigacion en Energia, Universidad Nacional Autonoma de Mexico, Privada Xochicalco S/N, Temixco, Morelos (Mexico); Gochi-Ponce, Y. [Instituto Tecnologico de Oaxaca, Division de Estudios de Posgrado e Investigacion, Ave. Ing. Victor Bravo Ahuja, esq. Ave. Tecnologico No. 120, Col. Centro. Oaxaca, Oax (Mexico); Contreras Larios, J.L. [Universidad Autonoma Metropolitana Azcapotzalco, CBI., Energia, Av. Sn. Pablo 180, Col. Reynosa, C.P. 02200, Mexico D.F (Mexico)

2010-11-15

Ni-W/Al{sub 2}O{sub 3} catalysts were synthesized, characterized and tested for the steam reforming of ethanol from 300 to 600 C. Addition of Ni and W on the alumina, decreased the surface area and increased the pore volume of the mesoporous materials synthesized. The reaction products obtained were: H{sub 2}, CO{sub 2}, C{sub 2}H{sub 4}, CH{sub 4}, CO{sub 2}, CO and CH{sub 3}CHO. A promoting effect of Ni-W was observed in the conversion of ethanol to H{sub 2} from 15 to 30 wt.% Ni and 1 wt.% W. The selectivity to H{sub 2} on the alumina with Ni-W, was between 66.53 and 68.53% at 550 C, appearing some undesirable products, with low ratio of CO/CO{sub 2}. Reaction was studied on a fixed bed reactor at atmospheric pressure with an ethanol/water molar ratio of 1:4, from 300 to 600 C. The catalysts were characterized by the thermal gravimetric analysis (TGA)-Differential thermal analysis (DTA), N{sub 2} physisorption (BET and BJH methods), X-ray diffraction (XRD) and scanning electron microscopy (SEM), these techniques were used for characterization, before and after of the steam reforming. (author)

Ethanol steam reforming kinetics of a Pd-Ag membrane reactor

NARCIS (Netherlands)

Tosti, S.; Basile, A.; Borelli, R.; Borgognoni, F.; Castelli, S.; Fabbricino, M.; Gallucci, F.; Licusati, C.

2009-01-01

The ethanol steam reforming reaction carried out in a Pd-based tubular membrane reactor has been modelled via a finite element code. The model considers the membrane tube divided into finite volume elements where the mass balances for both lumen and shell sides are carried out accordingly to the

Influence of Steam Reforming Catalyst Geometry on the Performance of Tubular Reformer – Simulation Calculations

Directory of Open Access Journals (Sweden)

Franczyk Ewelina

2015-06-01

Full Text Available A proper selection of steam reforming catalyst geometry has a direct effect on the efficiency and economy of hydrogen production from natural gas and is a very important technological and engineering issue in terms of process optimisation. This paper determines the influence of widely used seven-hole grain diameter (ranging from 11 to 21 mm, h/d (height/diameter ratio of catalyst grain and Sh/St (hole surface/total cylinder surface in cross-section ratio (ranging from 0.13 to 0.37 on the gas load of catalyst bed, gas flow resistance, maximum wall temperature and the risk of catalyst coking. Calculations were based on the one-dimensional pseudo-homogeneous model of a steam reforming tubular reactor, with catalyst parameters derived from our investigations. The process analysis shows that it is advantageous, along the whole reformer tube length, to apply catalyst forms of h/d = 1 ratio, relatively large dimensions, possibly high bed porosity and Sh/St ≈ 0.30-0.37 ratio. It enables a considerable process intensification and the processing of more natural gas at the same flow resistance, despite lower bed activity, without catalyst coking risk. Alternatively, plant pressure drop can be reduced maintaining the same gas load, which translates directly into diminishing the operating costs as a result of lowering power consumption for gas compression.

Feasability of the direct generation of hydrogen for fuel-cell-powered vehicles by on-board steam reforming of naphta

NARCIS (Netherlands)

Darwish, Naif A.; Hilal, Nidal; Versteeg, Geert; Heesink, Albertus B.M.

2004-01-01

A process flow sheet for the production of hydrogen to run a 50 kW fuel-cell-powered-vehicle by steam reforming of naphtha is presented. The major units in the flow sheet involve a desulfurization unit, a steam reformer, a low temperature (LT) shift reactor, a methanation reactor, and a membrane

Feasibility of the direct generation of hydrogen for fuel-cell-powered vehicles by on-board steam reforming of naphtha

NARCIS (Netherlands)

Darwish, Naif A.; Hilal, Nidal; Versteeg, Geert; Heesink, Bert

2004-01-01

A process flow sheet for the production of hydrogen to run a 50 kW fuel-cell-powered-vehicle by steam reforming of naphtha is presented. The major units in the flow sheet involve a desulfurization unit, a steam reformer, a low temperature (LT) shift reactor, a methanation reactor, and a membrane

Activity Tests of Macro-Meso Porous Catalysts over Metal Foam Plate for Steam Reforming of Bio-Ethanol.

Science.gov (United States)

Park, No-Kuk; Jeong, Yong Han; Kang, Misook; Lee, Tae Jin

2018-09-01

The catalytic activity of a macro-mesoporous catalyst coated on a metal foam plate in the reforming of bio-ethanol to synthesis gas was investigated. The catalysts were prepared by coating a support with a noble metal and transition metal. The catalytic activity for the production of synthetic gas by the reforming of bio-ethanol was compared according to the support material, reaction temperature, and steam/carbon ratio. The catalysts coated on the metal foams were prepared using a template method, in which macro-pores and meso-pores were formed by mixing polymer beads. In particular, the thermodynamic equilibrium composition of bio-ethanol reforming with the reaction temperature and steam/carbon ratio to produce synthetic gas was examined using the HSC (Enthalpy-Entropy-Heat capacity) chemistry program in this study. The composition of hydrogen and carbon monoxide in the reformate gas produced by steam reforming over the Rh/Ni-Ce-Zr/Al2O3-based pellet type catalysts and metal foam catalysts that had been coated with the Rh/Al-Ce-Zr-based catalysts was investigated by experimental activity tests. The activity of the metal foam catalyst was higher than that of the pellet type catalyst.

Steam reforming of different biomass tar model compounds over Ni/Al_2O_3 catalysts

International Nuclear Information System (INIS)

Artetxe, Maite; Alvarez, Jon; Nahil, Mohamad A.; Olazar, Martin; Williams, Paul T.

2017-01-01

Highlights: • Order of reactivity: anisole > furfural > indene > phenol > toluene > methyl naphthalene. • Higher coke deposition for oxygenates (1.5–2.8%) than for aromatics (0.5–0.8%). • Amorphous coke is deposited for oxygenates and filamentous carbon for aromatics. • Ni content of 20 wt.% shows the higher conversion (90%) and H_2 potential (63%). - Abstract: This work focuses on the removal of the tar derived from biomass gasification by catalytic steam reforming on Ni/Al_2O_3 catalysts. Different tar model compounds (phenol, toluene, methyl naphthalene, indene, anisole and furfural) were individually steam reformed (after dissolving each one in methanol), as well as a mixture of all of them, at 700 °C under a steam/carbon (S/C) ratio of 3 and 60 min on stream. The highest conversions and H_2 potential were attained for anisole and furfural, while methyl naphthalene presented the lowest reactivity. Nevertheless, the higher reactivity of oxygenates compared to aromatic hydrocarbons promoted carbon deposition on the catalyst (in the 1.5–2.8 wt.% range). When the concentration of methanol is decreased in the feedstock and that of toluene or anisole is increased, the selectivity to CO is favoured in the gaseous products, thus increasing coke deposition on the catalyst and decreasing catalyst activity for the steam reforming reaction. Moreover, an increase in Ni loading in the catalyst from 5 to 20% enhances carbon conversion and H_2 formation in the steam reforming of a mixture of all the model compounds studied, but these values decrease for a Ni content of 40%. Coke formation also increased by increasing Ni loading, attaining its maximum value for 40% Ni (6.5 wt.%).

Hydrogen production by enhanced-sorption chemical looping steam reforming of glycerol in moving-bed reactors

International Nuclear Information System (INIS)

Dou, Binlin; Song, Yongchen; Wang, Chao; Chen, Haisheng; Yang, Mingjun; Xu, Yujie

2014-01-01

Highlights: • New approach on continuous high-purity H 2 produced auto-thermally with long time. • Low-cost NiO/NiAl 2 O 4 exhibited high redox performance to H 2 from glycerol. • Oxidation, steam reforming, WSG and CO 2 capture were combined into a reactor. • H 2 purity of above 90% was produced without heating at 1.5–3.0 S/C and 500–600 °C. • Sorbent regeneration and catalyst oxidization achieved simultaneously in a reactor. - Abstract: The continuous high-purity hydrogen production by the enhanced-sorption chemical looping steam reforming of glycerol based on redox reactions integrated with in situ CO 2 removal has been experimentally studied. The process was carried out by a flow of catalyst and sorbent mixture using two moving-bed reactors. Various unit operations including oxidation, steam reforming, water gas shrift reaction and CO 2 removal were combined into a single reactor for hydrogen production in an overall economic and efficient process. The low-cost NiO/NiAl 2 O 4 catalyst efficiently converted glycerol and steam to H 2 by redox reactions and the CO 2 produced in the process was simultaneously removed by CaO sorbent. The best results with an enriched hydrogen product of above 90% in auto-thermal operation for reforming reactor were achieved at initial temperatures of 500–600 °C and ratios of steam to carbon (S/C) of 1.5–3.0. The results indicated also that not all of NiO in the catalyst can be reduced to Ni by the reaction with glycerol, and the reduced Ni can be oxidized to NiO by air at 900 °C. The catalyst oxidization and sorbent regeneration were achieved under the same conditions in air reactor

Influence of potassium on the competition between methane and ethane in steam reforming over Pt supported on yttrium-stabilized zirconia.

NARCIS (Netherlands)

Graf, P.O.; Mojet, Barbara; Lefferts, Leonardus

2008-01-01

effect of addition of potassium to Pt supported on yttrium-stabilized zirconia (PtYSZ) catalyst for steam reforming of methane, ethane and methane/ethane mixtures was explored. Addition of potassium has a positive effect on preferential steam reforming of methane in mixtures of methane and ethane

CATALYTIC STEAM REFORMING OF CHLOROCARBONS: POLYCHLORINATED BIPHENYLS (PCBS). (R826694C633)

Science.gov (United States)

Experiments with commercial askarals (Aroclors 1221, 1248 and 1254) have confirmed the feasibility of catalytic steam reforming as a method for destroying polychlorinated biphenyls (PCBs). Rhodium, platinum and nickel supported on A theoretical study on the structure dependence of the steam methane reforming reaction by rhodium

NARCIS (Netherlands)

Grootel, van P.W.

2012-01-01

Steam methane reforming is an important industrial reaction for the conversion of methane with steam to synthesis gas, a mixture of carbon monoxide and hydrogen. Hydrogen is used in many applications, e.g. for hydrogenation purposes. It is also used for the production of bulk chemicals such as

Solar membrane natural gas steam-reforming process: evaluation of reactor performance

NARCIS (Netherlands)

de Falco, M.; Basile, A.; Gallucci, F.

2010-01-01

In this work, the performance of an innovative plant for efficient hydrogen production using solar energy for the process heat duty requirements has been evaluated via a detailed 2D model. The steam-reforming reactor consists of a bundle of coaxial double tubes assembled in a shell. The annular

Solar membrane natural gas steam-reforming process : evaluation of reactor performance

NARCIS (Netherlands)

Falco, de M.; Basile, A.; Gallucci, F.

2010-01-01

In this work, the performance of an innovative plant for efficient hydrogen production using solar energy for the process heat duty requirements has been evaluated via a detailed 2D model. The steam-reforming reactor consists of a bundle of coaxial double tubes assembled in a shell. The annular

CATALYTIC STEAM REFORMING OF CHLOROCARBONS: CATALYST COMPARISONS. (R826694C633)

Science.gov (United States)

Catalyst candidates for steam reforming chlorocarbons have been screened for activity using methyl chloride as a model reactant. At 500°C, a H2O/C ratio of about 10 and a GHSV of 254 000 h-1, catalysts comprising 0.5% loading of the metals ...

Effect of a diffuser on performance enhancement of a cylindrical methanol steam reformer by computational fluid dynamic analysis

International Nuclear Information System (INIS)

Perng, Shiang-Wuu; Horng, Rong-Fang; Wu, Horng-Wen

2017-01-01

Highlights: •We enhance performance of a cylindrical MSR to get higher net power of fuel cell. •We study diffuser angle and length and wall temperature on net power of fuel cell. •We study methanol conversion, hydrogen production, CO of a novel reformer. •Diffuser in catalyst bed upstream raises methanol conversion, hydrogen production. •The MSR raises hydrogen production up to 44.6% and net fuel cell power up to 24.6%. -- Abstract: Proton exchange membrane fuel cells (PEMFC) connected with a methanol steam reformer designed to enhance its performance is considered as a promising future power source. Enhancing the performance of a cylindrical methanol steam reformer due to diffuser effects was then investigated applying three-dimensional computational fluid dynamics by the SIMPLE-C algorithm and an Arrhenius form of reaction model. The effect of the angle and length of the diffuser, and wall temperature have been explored on heat and fluid flow, methanol conversion, hydrogen production, carbon monoxide reduction, as well as estimated net power of fuel cell with the same catalyst volume and entrance condition in a cylindrical methanol steam reformer. The results indicate that the diffuser obviously enhances methanol conversion and hydrogen production of a cylindrical methanol steam reformer. In comparison with a traditional reformer, the reformer with a diffuser of θ d = 6° and L d = 75 mm obtains the maximum enhancement of 22.96% in methanol conversion, 44.62% in hydrogen production, and 24.59% in estimated net power of fuel cell at wall temperature of 250 °C. In addition, the novel reformer with a diffuser of θ d = 9° and L d = 100 mm generates the maximum reduction of 44.17% in CO production at T W = 250 °C.

Plasma steam reforming of E85 for hydrogen rich gas production

International Nuclear Information System (INIS)

Zhu Xinli; Hoang Trung; Lobban, Lance L; Mallinson, Richard G

2011-01-01

E85 (85 vol% ethanol and 15 vol% gasoline) is a partly renewable fuel that is increasing in supply availability. Hydrogen production from E85 for fuel cell or internal combustion engine applications is a potential method for reducing CO 2 emissions. Steam reforming of E85 using a nonthermal plasma (pulse corona discharge) reactor has been exploited at low temperature (200-300 0 C) without external heating, diluent gas, oxidant or catalyst in this work. Several operational parameters, including the discharge current, E85 concentration and feed flow rate, have been investigated. The results show that hydrogen rich gases (63-67% H 2 and 22-29% CO, with small amounts of CO 2 , C 2 hydrocarbons and CH 4 ) can be produced by this method. A comparison with ethanol reforming and gasoline reforming under identical conditions has also been made and the behaviour of E85 reforming is found to be close to that of ethanol reforming with slightly higher C 2 hydrocarbons yields.

A Numerical Study on Mass Transfer and Methanol Conversion Efficiency According to Porosity and Temperature Change of Curved Channel Methanol-Steam Reformer

Energy Technology Data Exchange (ETDEWEB)

Seong, Hong Seok; Lee, Chung Ho; Suh, Jeong Se [Gyeongsang Nat’l Univ., Jinju (Korea, Republic of)

2016-11-15

Micro methanol-steam reformer for fuel cell can effectively produce hydrogen as reforming response to steam takes place in low temperature (less than 250℃). This study conducted numerical research on this reformer. First, study set wall temperature of the reformer at 100, 140, 180 and 220℃ while methanol conversion efficiency was set in 0, 0.072, 3.83 and 46.51% respectively. Then, porosity of catalyst was set in 0.1, 0.35, 0.6 and 0.85 and although there was no significant difference in methanol conversion efficiency, values of pressure drop were 4645.97, 59.50, 5.12 and 0.45 kPa respectively. This study verified that methanol-steam reformer rarely responds under the temperature of 180℃ and porosity does not have much effect on methanol conversion efficiency if the fluid flowing through reformer lowers activation energy by sufficiently contacting reformer.

A Numerical Study on Mass Transfer and Methanol Conversion Efficiency According to Porosity and Temperature Change of Curved Channel Methanol-Steam Reformer

International Nuclear Information System (INIS)

Seong, Hong Seok; Lee, Chung Ho; Suh, Jeong Se

2016-01-01

Micro methanol-steam reformer for fuel cell can effectively produce hydrogen as reforming response to steam takes place in low temperature (less than 250℃). This study conducted numerical research on this reformer. First, study set wall temperature of the reformer at 100, 140, 180 and 220℃ while methanol conversion efficiency was set in 0, 0.072, 3.83 and 46.51% respectively. Then, porosity of catalyst was set in 0.1, 0.35, 0.6 and 0.85 and although there was no significant difference in methanol conversion efficiency, values of pressure drop were 4645.97, 59.50, 5.12 and 0.45 kPa respectively. This study verified that methanol-steam reformer rarely responds under the temperature of 180℃ and porosity does not have much effect on methanol conversion efficiency if the fluid flowing through reformer lowers activation energy by sufficiently contacting reformer.

Radioactive demonstration of final mineralized waste forms for Hanford waste treatment plant secondary waste (WTP-SW) by fluidized bed steam reforming (FBSR) using the bench scale reformer platform

Energy Technology Data Exchange (ETDEWEB)

Crawford, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Burket, P. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Cozzi, A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Daniel, G. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Jantzen, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Missimer, D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2014-08-01

The U.S. Department of Energy’s Office of River Protection (ORP) is responsible for the retrieval, treatment, immobilization, and disposal of Hanford’s tank waste. Currently there are approximately 56 million gallons of highly radioactive mixed wastes awaiting treatment. A key aspect of the River Protection Project (RPP) cleanup mission is to construct and operate the Waste Treatment and Immobilization Plant (WTP). The WTP will separate the tank waste into high-level and low-activity waste (LAW) fractions, both of which will subsequently be vitrified. The projected throughput capacity of the WTP LAW Vitrification Facility is insufficient to complete the RPP mission in the time frame required by the Hanford Federal Facility Agreement and Consent Order, also known as the Tri-Party Agreement (TPA), i.e. December 31, 2047. Therefore, Supplemental Treatment is required both to meet the TPA treatment requirements as well as to more cost effectively complete the tank waste treatment mission. In addition, the WTP LAW vitrification facility off-gas condensate known as WTP Secondary Waste (WTP-SW) will be generated and enriched in volatile components such as 137Cs, 129I, 99Tc, Cl, F, and SO4 that volatilize at the vitrification temperature of 1150°C in the absence of a continuous cold cap (that could minimize volatilization). The current waste disposal path for the WTP-SW is to process it through the Effluent Treatment Facility (ETF). Fluidized Bed Steam Reforming (FBSR) is being considered for immobilization of the ETF concentrate that would be generated by processing the WTP-SW. The focus of this current report is the WTP-SW.

Bench scale demonstration and conceptual engineering for DETOXSM catalyzed wet oxidation

International Nuclear Information System (INIS)

Moslander, J.; Bell, R.; Robertson, D.; Dhooge, P.; Goldblatt, S.

1994-01-01

Laboratory and bench scale studies of the DETOX SM catalyzed wet oxidation process have been performed with the object of developing the process for treatment of hazardous and mixed wastes. Reaction orders, apparent rates, and activation energies have been determined for a range of organic waste surrogates. Reaction intermediates and products have been analyzed. Metals' fates have been determined. Bench scale units have been designed, fabricated, and tested with solid and liquid organic waste surrogates. Results from the laboratory and bench scale studies have been used to develop conceptual designs for application of the process to hazardous and mixed wastes

CATALYTIC STEAM REFORMING OF CHLOROCARBONS: CATALYST COMPARISONS. (R822721C633)

Science.gov (United States)

Catalyst candidates for steam reforming chlorocarbons have been screened for activity using methyl chloride as a model reactant. At 500°C, a H2O/C ratio of about 10 and a GHSV of 254 000 h-1, catalysts comprising 0.5% loading of the metals o...

Hierarchically structured catalysts for cascade and selective steam reforming/hydrodeoxygenation reactions.

Science.gov (United States)

Sun, Junming; Karim, Ayman M; Li, Xiaohong Shari; Rainbolt, James; Kovarik, Libor; Shin, Yongsoon; Wang, Yong

2015-12-04

We report a hierarchically structured catalyst with steam reforming and hydrodeoxygenation functionalities being deposited in the micropores and macropores, respectively. The catalyst is highly efficient to upgrade the pyrolysis vapors of pine forest product residual, resulting in a dramatically decreased acid content and increased hydrocarbon yield without external H2 supply.

Bench-scale Kinetics Study of Mercury Reactions in FGD Liquors

Energy Technology Data Exchange (ETDEWEB)

Gary Blythe; John Currie; David DeBerry

2008-03-31

This document is the final report for Cooperative Agreement DE-FC26-04NT42314, 'Kinetics Study of Mercury Reactions in FGD Liquors'. The project was co-funded by the U.S. DOE National Energy Technology Laboratory and EPRI. The objective of the project has been to determine the mechanisms and kinetics of the aqueous reactions of mercury absorbed by wet flue gas desulfurization (FGD) systems, and develop a kinetics model to predict mercury reactions in wet FGD systems. The model may be used to determine optimum wet FGD design and operating conditions to maximize mercury capture in wet FGD systems. Initially, a series of bench-top, liquid-phase reactor tests were conducted and mercury species concentrations were measured by UV/visible light spectroscopy to determine reactant and byproduct concentrations over time. Other measurement methods, such as atomic absorption, were used to measure concentrations of vapor-phase elemental mercury, that cannot be measured by UV/visible light spectroscopy. Next, a series of bench-scale wet FGD simulation tests were conducted. Because of the significant effects of sulfite concentration on mercury re-emission rates, new methods were developed for operating and controlling the bench-scale FGD experiments. Approximately 140 bench-scale wet FGD tests were conducted and several unusual and pertinent effects of process chemistry on mercury re-emissions were identified and characterized. These data have been used to develop an empirically adjusted, theoretically based kinetics model to predict mercury species reactions in wet FGD systems. The model has been verified in tests conducted with the bench-scale wet FGD system, where both gas-phase and liquid-phase mercury concentrations were measured to determine if the model accurately predicts the tendency for mercury re-emissions. This report presents and discusses results from the initial laboratory kinetics measurements, the bench-scale wet FGD tests, and the kinetics modeling

Steam and partial oxidation reforming options for hydrogen production from fossil fuels for PEM fuel cells

Directory of Open Access Journals (Sweden)

Yousri M.A. Welaya

2012-06-01

Full Text Available Proton exchange membrane fuel cell (PEM generates electrical power from air and from hydrogen or hydrogen rich gas mixtures. Therefore, there is an increasing interest in converting current hydrocarbon based marine fuels such as natural gas, gasoline, and diesel into hydrogen rich gases acceptable to the PEM fuel cells on board ships. Using chemical flow sheeting software, the total system efficiency has been calculated. Natural gas appears to be the best fuel for hydrogen rich gas production due to its favorable composition of lower molecular weight compounds. This paper presents a study for a 250 kW net electrical power PEM fuel cell system utilizing a partial oxidation in one case study and steam reformers in the second. This study has shown that steam-reforming process is the most competitive fuel processing option in terms of fuel processing efficiency. Partial oxidation process has proved to posses the lowest fuel processing efficiency. Among the options studied, the highest fuel processing efficiency is achieved with natural gas steam reforming system.

Stable hydrogen production from ethanol through steam reforming reaction over nickel-containing smectite-derived catalyst.

Science.gov (United States)

Yoshida, Hiroshi; Yamaoka, Ryohei; Arai, Masahiko

2014-12-25

Hydrogen production through steam reforming of ethanol was investigated with conventional supported nickel catalysts and a Ni-containing smectite-derived catalyst. The former is initially active, but significant catalyst deactivation occurs during the reaction due to carbon deposition. Side reactions of the decomposition of CO and CH4 are the main reason for the catalyst deactivation, and these reactions can relatively be suppressed by the use of the Ni-containing smectite. The Ni-containing smectite-derived catalyst contains, after H2 reduction, stable and active Ni nanocrystallites, and as a result, it shows a stable and high catalytic performance for the steam reforming of ethanol, producing H2.

Performance and economic assessments of a solid oxide fuel cell system with a two-step ethanol-steam-reforming process using CaO sorbent

Science.gov (United States)

Tippawan, Phanicha; Arpornwichanop, Amornchai

2016-02-01

The hydrogen production process is known to be important to a fuel cell system. In this study, a carbon-free hydrogen production process is proposed by using a two-step ethanol-steam-reforming procedure, which consists of ethanol dehydrogenation and steam reforming, as a fuel processor in the solid oxide fuel cell (SOFC) system. An addition of CaO in the reformer for CO2 capture is also considered to enhance the hydrogen production. The performance of the SOFC system is analyzed under thermally self-sufficient conditions in terms of the technical and economic aspects. The simulation results show that the two-step reforming process can be run in the operating window without carbon formation. The addition of CaO in the steam reformer, which runs at a steam-to-ethanol ratio of 5, temperature of 900 K and atmospheric pressure, minimizes the presence of CO2; 93% CO2 is removed from the steam-reforming environment. This factor causes an increase in the SOFC power density of 6.62%. Although the economic analysis shows that the proposed fuel processor provides a higher capital cost, it offers a reducing active area of the SOFC stack and the most favorable process economics in term of net cost saving.

Design of a surface alloy catalyst for steam reforming

DEFF Research Database (Denmark)

Besenbacher, F.; Chorkendorff, Ib; Clausen, B.S.

1998-01-01

Detailed studies of elementary chemical processes on well-characterized single crystal surfaces have contributed substantially to the understanding of heterogeneous catalysis. insight into the structure of surface alloys combined with an understanding of the relation between the surface compositi...... and reactivity is shown to lead directly to new ideas for catalyst design, The feasibility of such an approach is illustrated by the synthesis, characterization, and tests of a high-surface area gold-nickel catalyst for steam reforming....

Catalytic steam reforming of tar derived from steam gasification of sunflower stalk over ethylene glycol assisting prepared Ni/MCM-41

International Nuclear Information System (INIS)

Karnjanakom, Surachai; Guan, Guoqing; Asep, Bayu; Du, Xiao; Hao, Xiaogang; Samart, Chanatip; Abudula, Abuliti

2015-01-01

Highlights: • Ni/MCM-41 was prepared by EG-assisted co-impregnation method. • EG-assisted co-impregnation method resulted in Ni particles well dispersed on MCM-41. • Ni/MCM-41-EG catalyst had high catalytic activity for tar reforming. • The highest H 2 gas yield was obtained when using 20 wt.% Ni/MCM-41-EG. • The catalysts were reused up to 5 cycles without any serious deactivation. - Abstract: Ethylene glycol (EG) assisted impregnation of nickel catalyst on MCM-41 (Ni/MCM-41-EG) was performed and applied for steam reforming of tar derived from biomass. The catalyst was characterized by SEM–EDX, BET, XRD, and TPR. It is found that smaller nickel particles were well dispersed on MCM-41 and better catalytic activity was shown for the Ni/MCM-41-EG when compared with the catalyst of Ni/MCM-41 prepared by using the conventional impregnation method. H 2 yield increased approximately 8% when using 20 wt.% Ni/MCM-41-EG instead of 20 wt.% Ni/MCM-41 for the steam reforming of tar derived from sunflower stalk. The catalyst reusability was also tested up to five cycles, and no obvious activity reduction was observed. It indicates that EG assisted impregnation method is a good way to prepare metal loaded porous catalyst with high catalytic activity, high loading amount and long-term stability for the tar reforming

Steam reforming of ethanol over Co3O4–Fe2O3 mixed oxides

KAUST Repository

Abdelkader, A.; Daly, H.; Saih, Y.; Morgan, K.; Mohamed, M.A.; Halawy, S.A.; Hardacre, C.

2013-01-01

solvent/dispersing agent. The catalysts were studied in the steam reforming of ethanol to investigate the effect of the partial substitution of Co3O4 with Fe2O 3 on the catalytic behaviour. The reforming activity over Fe 2O3, while initially high

Ethanol steam reforming kinetics of a Pd-Ag membrane reactor

Energy Technology Data Exchange (ETDEWEB)

Tosti, Silvano; Borelli, Rodolfo; Borgognoni, Fabio [ENEA, Dipartimento FPN, C.R. ENEA Frascati, Via E. Fermi 45, Frascati (RM) I-00044 (Italy); Basile, Angelo [Institute on Membrane Technology, ITM-CNR, c/o Univ. of Calabria, via P. Bucci, Cubo 17/C, 87030 Rende (CS) (Italy); Castelli, Stefano [ENEA, Dipartimento ACS, C.R. ENEA Casaccia, Via Anguillarese 301, Roma I-00123 (Italy); Fabbricino, Massimiliano; Licusati, Celeste [Dept. of Hydraulic and Environmental Engineering, Univ. of Naples Federico II, Via Claudio 21, Naples 80125 (Italy); Gallucci, Fausto [Fundamentals of Chemical Reaction Engineering Group, Faculty of Science and Technology, University of Twente, Enschede (Netherlands)

2009-06-15

The ethanol steam reforming reaction carried out in a Pd-based tubular membrane reactor has been modelled via a finite element code. The model considers the membrane tube divided into finite volume elements where the mass balances for both lumen and shell sides are carried out accordingly to the reaction and permeation kinetics. Especially, a simplified ''power law'' has been applied for the reaction kinetics: the comparison with experimental data obtained by using three different kinds of catalyst (Ru, Pt and Ni based) permitted defining the coefficients of the kinetics expression as well as to validate the model. Based on the Damkohler-Peclet analysis, the optimization of the membrane reformer has been also approached. (author)

CATALYTIC STEAM REFORMING OF CHLOROCARBONS: TRICHLOROETHANE, TRICHLOROETHYLENE AND PERCHLOROETHYLENE. (R826694C633)

Science.gov (United States)

The effective destruction of trichloroethane, trichloroethylene and perchloroethylene by steam reforming with a commercial nickel catalyst has been demonstrated. Conversion levels of up to 0.99999 were attained in both laboratory and semi-pilot experiments, with the products c...

A dense Pd/Ag membrane reactor for methanol steam reforming: Experimental study

NARCIS (Netherlands)

Basile, A.; Gallucci, F.; Paturzo, L.

2005-01-01

This paper focuses on an experimental study of the methanol steam reforming (MSR) reaction. A dense Pd/Ag membrane reactor (MR) has been used, and its behaviour has been compared to the performance of a traditional reactor (TR) packed with the same catalyst type and amount. The parameters

Poly-dimethylsiloxane (PDMS) based micro-reactors for steam reforming of methanol

Energy Technology Data Exchange (ETDEWEB)

Ha, Ji Won; Kundu, Arunabha; Jang, Jae Hyuk

2010-11-15

A miniaturized methanol steam reformer with a serpentine type of micro-channels was developed based on poly-dimethylsiloxane (PDMS) material. This way of fabricating micro-hydrogen generator is very simple and inexpensive. The volume of a PDMS micro-reformer is less than 10 cm{sup 3}. The catalyst used was a commercial Cu/ZnO/Al{sub 2}O{sub 3} reforming catalyst from Johnson Matthey. The Cu/ZnO/Al{sub 2}O{sub 3} reforming catalyst particles of mean diameter 50-70 {mu}m was packed into the micro-channels by injecting water based suspension of catalyst particles at the inlet point. The miniaturized PDMS micro-reformer was operated successfully in the operating temperatures of 180-240 C and 15%-75% molar methanol conversion was achieved in this temperature range for WHSV of 2.1-4.2 h{sup -1}. It was not possible to operate the micro-reformer made by pure PDMS at temperature beyond 240 C. Hybrid type of micro-reformer was fabricated by mixing PDMS and silica powder which allowed the operating temperature around 300 C. The complete conversion (99.5%) of methanol was achieved at 280 C in this case. The maximum reformate gas flow rate was 30 ml/min which can produce 1 W power at 0.6 V assuming hydrogen utilization of 60%. (author)

Coupling of a 2.5 kW steam reformer with a 1 kW el PEM fuel cell

Science.gov (United States)

Mathiak, J.; Heinzel, A.; Roes, J.; Kalk, Th.; Kraus, H.; Brandt, H.

The University of Duisburg-Essen has developed a compact multi-fuel steam reformer suitable for natural gas, propane and butane. This steam reformer was combined with a polymer electrolyte membrane fuel cell (PEM FC) and a system test of the process chain was performed. The fuel processor comprises a prereformer step, a primary reformer, water gas shift reactors, a steam generator, internal heat exchangers in order to achieve an optimised heat integration and an external burner for heat supply as well as a preferential oxidation step (PROX) as CO purification. The fuel processor is designed to deliver a thermal hydrogen power output from 500 W to 2.5 kW. The PEM fuel cell stack provides about 1 kW electrical power. In the following paper experimental results of measurements of the single components PEM fuel cell and fuel processor as well as results of the coupling of both to form a process chain are presented.

Fluidized Bed Steam Reforming For Treatment And Immobilization Of Low-Activity Waste

International Nuclear Information System (INIS)

Hewitt, W.M.

2011-01-01

This report is one of four reports written to provide background information regarding immobilization technologies remaining under consideration for supplemental immobilization of Hanford's low-activity waste. This paper provides the reader a general understanding of fluidized bed steam reforming and its possible application to treat and immobilize Hanford low-activity waste.

Life Cycle Assessment of Hydrogen Production via Natural Gas Steam Reforming; TOPICAL

International Nuclear Information System (INIS)

Spath, P. L.; Mann, M. K.

2000-01-01

A life cycle assessment of hydrogen production via natural gas steam reforming was performed to examine the net emissions of greenhouse gases as well as other major environmental consequences. LCA is a systematic analytical method that helps identify and evaluate the environmental impacts of a specific process or competing processes

Ni Catalysts Supported on Modified Alumina for Diesel Steam Reforming

Directory of Open Access Journals (Sweden)

Antonios Tribalis

2016-01-01

Full Text Available Nickel catalysts are the most popular for steam reforming, however, they have a number of drawbacks, such as high propensity toward coke formation and intolerance to sulfur. In an effort to improve their behavior, a series of Ni-catalysts supported on pure and La-, Ba-, (La+Ba- and Ce-doped γ-alumina has been prepared. The doped supports and the catalysts have been extensively characterized. The catalysts performance was evaluated for steam reforming of n-hexadecane pure or doped with dibenzothiophene as surrogate for sulphur-free or commercial diesel, respectively. The undoped catalyst lost its activity after 1.5 h on stream. Doping of the support with La improved the initial catalyst activity. However, this catalyst was completely deactivated after 2 h on stream. Doping with Ba or La+Ba improved the stability of the catalysts. This improvement is attributed to the increase of the dispersion of the nickel phase, the decrease of the support acidity and the increase of Ni-phase reducibility. The best catalyst of the series doped with La+Ba proved to be sulphur tolerant and stable for more than 160 h on stream. Doping of the support with Ce also improved the catalytic performance of the corresponding catalyst, but more work is needed to explain this behavior.

MINERALIZING, STEAM REFORMING TREATMENT OF HANFORD LOW-ACTIVITY WASTE (a.k.a. INEEL/EXT-05-02526)

International Nuclear Information System (INIS)

A. L. Olson; N. R. Soelberg; D. W. Marshall; G. L. Anderson

2005-01-01

The U.S. Department of Energy (DOE) documented, in 2002, a plan for accelerating cleanup of the Hanford Site, located in southeastern Washington State, by at least 35 years. A key element of the plan was acceleration of the tank waste program and completion of ''tank waste treatment by 2028 by increasing the capacity of the planned Waste Treatment Plant (WTP) and using supplemental technologies for waste treatment and immobilization''. The plan identified steam reforming technology as a candidate for supplemental treatment of as much as 70% of the low-activity waste (LAW). Mineralizing steam reforming technology, offered by THOR Treatment Technologies, LLC would produce a denitrated, granular mineral waste form using a high-temperature fluidized bed process. A pilot scale demonstration of the technology was completed in a 15-cm-diameter reactor vessel. The pilot scale facility was equipped with a cyclone separator and heated sintered metal filters for particulate removal, a thermal oxidizer for reduced gas species and NOx destruction, and a packed activated carbon bed for residual volatile species capture. The pilot scale equipment is owned by the DOE, but located at the Science and Technology Applications Research (STAR) Center in Idaho Falls, ID. Pilot scale testing was performed August 2-5, 2004. Flowsheet chemistry and operational parameters were defined through a collaborative effort involving Idaho National Engineering and Environmental Laboratory (INEEL), Savannah River National Laboratory (SRNL), and THOR Treatment Technologies personnel. Science Application International Corporation, owners of the STAR Center, personnel performed actual pilot scale operation. The pilot scale test achieved a total of 68.4 hours of cumulative/continuous processing operation before termination in response to a bed de-fluidization condition. 178 kg of LAW surrogate were processed that resulted in 148 kg of solid product, a mass reduction of about 17%. The process achieved

FLUIDIZED BED STEAM REFORMING FOR TREATMENT AND IMMOBILIZATION OF LOW-ACTIVITY WASTE

Energy Technology Data Exchange (ETDEWEB)

HEWITT WM

2011-04-08

This report is one of four reports written to provide background information regarding immobilization technologies remaining under consideration for supplemental immobilization of Hanford's low-activity waste. This paper provides the reader a general understanding of fluidized bed steam reforming and its possible application to treat and immobilize Hanford low-activity waste.

Internal steam reforming in solid oxide fuel cells: Status and opportunities of kinetic studies and their impact on modelling

DEFF Research Database (Denmark)

Mogensen, David; Grunwaldt, J.-D.; Hendriksen, Peter Vang

2011-01-01

Solid oxide fuel cells (SOFC) systems with internal steam reforming have the potential to become an economically competitive technology for cogeneration power plants, exploiting its significantly higher electrical efficiency compared to existing technologies. Optimal design and operation of such ......Solid oxide fuel cells (SOFC) systems with internal steam reforming have the potential to become an economically competitive technology for cogeneration power plants, exploiting its significantly higher electrical efficiency compared to existing technologies. Optimal design and operation...

Synthesis gas production via hybrid steam reforming of natural gas and bio-liquids

NARCIS (Netherlands)

Balegedde Ramachandran, P.

2013-01-01

This thesis deals with (catalytic) steam reforming of bio-liquids for the production of synthesis gas. Glycerol, both crude from the biodiesel manufacturing and refined, and pyrolysis oil are tested as bio-based feedstocks. Liquid bio-based feeds could be preferred over inhomogeneous fibrous solid

Hydrogen from biomass gas steam reforming for low temperature fuel cell: energy and exergy analysis

Directory of Open Access Journals (Sweden)

A. Sordi

2009-03-01

Full Text Available This work presents a method to analyze hydrogen production by biomass gasification, as well as electric power generation in small scale fuel cells. The proposed methodology is the thermodynamic modeling of a reaction system for the conversion of methane and carbon monoxide (steam reforming, as well as the energy balance of gaseous flow purification in PSA (Pressure Swing Adsorption is used with eight types of gasification gases in this study. The electric power is generated by electrochemical hydrogen conversion in fuel cell type PEMFC (Proton Exchange Membrane Fuel Cell. Energy and exergy analyses are applied to evaluate the performance of the system model. The simulation demonstrates that hydrogen production varies with the operation temperature of the reforming reactor and with the composition of the gas mixture. The maximum H2 mole fraction (0.6-0.64 mol.mol-1 and exergetic efficiency of 91- 92.5% for the reforming reactor are achieved when gas mixtures of higher quality such as: GGAS2, GGAS4 and GGAS5 are used. The use of those gas mixtures for electric power generation results in lower irreversibility and higher exergetic efficiency of 30-30.5%.

Co-current and Counter-Current Operations for Steam Reforming of Heptane in a Novel CFB Membrane Reformer

International Nuclear Information System (INIS)

Chen, Z.; Elnashaie, S.S.E.H.

2004-01-01

Hydrogen production by steam reforming of higher hydrocarbon over nickel supported catalyst is investigated in an earlier suggested novel Circulating Fast Fluidized Bed Membrane Reformer (CFFBMR). Palladium hydrogen membranes are used with co-current and counter-current operation modes. It is found that hydrogen production has a non-monotonic dependence upon the reaction temperature in the range of 623-823 K. Between 623 and 723 K. the yields of hydrogen decrease and then increase between 723 and 823 K. This important phenomenon is investigated, discussed and explained. The simulation results shows that the reformer performance can be significantly improved using hydrogen membranes, especially in the counter-current operation mode. At low temperatures around 623 K, both .co-current and counter-current operation modes provide similar yields of hydrogen. While at temperature 723 K and higher, the counter-current operation provides the highest yield of hydrogen

Thermodynamic investigation and environment impact assessment of hydrogen production from steam reforming of poultry tallow

International Nuclear Information System (INIS)

Hajjaji, Noureddine

2014-01-01

Highlights: • Thermodynamic analysis and environmental impact assessment of H 2 production system. • Thermodynamic analysis identifies optimal conditions for H 2 production. • LCA is applied to evaluate the environmental impacts of H 2 production system. • Inventories data are derived from process simulation and from literature review. • Thermal energy process is the main contributor to the environmental impact. - Abstract: In this research, various assessment tools are applied to comprehensively investigate hydrogen production from steam reforming of poultry tallow (PT). These tools investigate the chemical reactions, design and simulate the entire hydrogen production process, study the energetic performance and perform an environment impact assessment using life cycle assessment (LCA) methodology. The chemical reaction investigation identifies thermodynamically optimal operating conditions at which PT may be converted to hydrogen via the steam reforming process. The synthesis gas composition was determined by simulations to minimize the Gibbs free energy using the Aspen Plus™ 10.2 software. These optimal conditions are, subsequently, used in the design and simulation of the entire PT-to-hydrogen process. LCA is applied to evaluate the environmental impacts of PT-to-hydrogen system. The system boundaries include rendering and reforming along with the required transportation process. The reforming inventories data are derived from process simulation in Aspen Plus™, whereas the rendering data are adapted from a literature review. The life cycle inventories data of PT-to-hydrogen are computationally implemented into SimaPro 7.3. A set of seven relevant environmental impact categories are evaluated: global warming, abiotic depletion, acidification, eutrophication, ozone layer depletion, photochemical oxidant formation, and cumulative non-renewable fossil and nuclear energy demand. The results are subject to a systematic sensitivity analysis and compared

Catalytic activity of catalysts for steam reforming reaction. Contract research

Energy Technology Data Exchange (ETDEWEB)

Ohashi, Hirofumi; Inagaki, Yoshiyuki [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment

2003-05-01

Japan Atomic Energy Research Institute has been developing a hydrogen production system by means of steam reforming of methane (chemical reation: CH{sub 4} + H{sub 2}O = CO + 3H{sub 2}) coupling with High Temperature Engineering Test Reactor (HTTR) to demonstrate effectiveness of high-temperature nuclear heat utilization. Prior to construction of HTTR hydrogen production system, a mock-up test facility with a full-scale reaction tube was constructed to investigate transient behavior of the hydrogen production system an establish system controllability. In order to predict transient behavior and hydrogen productivity of the hydrogen production system, it is important to estimate the reaction characteristics under the same temperature and pressure conditions as those of HTTR hydrogen production system. For the purpose of investigate an apparent activation energy of catalysts, catalytic activity test using small apparatus was carried out under the condition of methane flow rate from 1.18 x 10{sup -3} to 3.19 x 10{sup -3} mol/s, temperature from 500 to 900degC, pressure from 1.1 to 4.1MPa, and mol ratio of steam to methane from 2.5 to 3.5. It was confirmed that apparent activation energies of two kinds of Ni catalysts which are to be used in the mock-up test were 51.7 and 57.4kJ/mol, respectively, and reaction rate constants were propositional to the value from P{sup -0.15} to P{sup -0.33}. (author)

Proposal and assessment of a novel integrated CCHP system with biogas steam reforming using solar energy

International Nuclear Information System (INIS)

Su, Bosheng; Han, Wei; Jin, Hongguang

2017-01-01

Highlights: •A novel CCHP system with biogas steam reforming using solar energy is raised. •Chemical and physical energy of biogas is efficiently used in a cascaded way. •The energy quality of concentrating solar heat is promoted in the system. •A parametric analysis is adopted to optimize the thermodynamic performance. •A typical-day study is conducted to explore the general operation features. -- Abstract: The conventional way to utilize biogas either is energy-intensive due to biogas upgrading or causes huge waste of energy grade and environmental pollution by direct burning. This paper proposes a biogas and solar energy-assisted combined cooling, heating and power (BSCCHP) system that upgrades the caloric value of biogas before combustion by introducing a thermochemical conversion process that is driven by solar heat. Adopting commercially established technologies including steam reforming and parabolic dish concentrators, the system exhibits an enhanced system exergy efficiency, and the technology considerably reduces the direct CO 2 footprint and saves depletable fossil fuel. With a solar thermal share of 22.2%, the proposed system not only has a high net solar-to-product thermal and exergy efficiency of 46.80% and 26.49%, respectively, but also results in a commensurate 18.27% reduction of the direct CO 2 footprint compared with the reference individual systems. The effect of critical parameters in the biogas steam reforming process on the system performance was studied. A proper selection of the steam/carbon ratio leads to the optimal direct CO 2 footprint and system exergy efficiency. Pursuing a very high conversion of biogas by improving the reforming temperature is not a wise choice from a system perspective. Finally, a typical-day dynamic simulation was conducted to preliminarily explore the general operation features. This study may provide a new way to efficiently use the renewable energy in the distributed energy system.

Study on saccharification of cellulosic wastes with bench scale test plant, (5)

International Nuclear Information System (INIS)

Kasai, Noboru; Tamada, Masao; Kumakura, Minoru

1989-05-01

This report completed the results that were obtained on the studies of continuous saccharification of radiation pretreated chaff with a saccharification equipment unit of bench scale test plant for cellulosic wastes. The problem on the continuous saccharification in bench scale and its countermeasure were clarified. The glucose concentration obtained in the continuous saccharification was examined from the point of a scale up effect. It was found that there are not a scale up effect between flask scale (100 ml) and bench scale (50 l) and then the same concentration of glucose was obtained in both scales. It was clarified that the contamination of the process let decrease markedly the concentration of produced glucose solution and brings on a large trouble for the saccharification. The addition of 1 % ethyl acetate made it possible to prevent the contamination of the saccharification process in flask scale. However, in the case of continuous saccharification in bench scale, the addition of ethyl acetate in nitrogen gas atmosphere was necessary to prevent the contamination. It was found that the solution of 1.7 % glucose concentration was continuously produced in the continuous saccharification with the most longest period for 26 days. It was, also, suggested that the selection of a suitable retention time is necessary to attain a high glucose productivity in the continuous saccharification. (author)

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. Copyright © 2016 Elsevier Ltd. All rights reserved.

Numerical study of methanol–steam reforming and methanol–air catalytic combustion in annulus reactors for hydrogen production

International Nuclear Information System (INIS)

Chein, Reiyu; Chen, Yen-Cho; Chung, J.N.

2013-01-01

Highlights: ► Performance of mini-scale integrated annulus reactors for hydrogen production. ► Flow rates fed to combustor and reformer control the reactor performance. ► Optimum performance is found from balance of flow rates to combustor and reformer. ► Better performance can be found when shell side is designed as combustor. -- Abstract: This study presents the numerical simulation on the performance of mini-scale reactors for hydrogen production coupled with liquid methanol/water vaporizer, methanol/steam reformer, and methanol/air catalytic combustor. These reactors are designed similar to tube-and-shell heat exchangers. The combustor for heat supply is arranged as the tube or shell side. Based on the obtained results, the methanol/air flow rate through the combustor (in terms of gas hourly space velocity of combustor, GHSV-C) and the methanol/water feed rate to the reformer (in terms of gas hourly space velocity of reformer, GHSV-R) control the reactor performance. With higher GHSV-C and lower GHSV-R, higher methanol conversion can be achieved because of higher reaction temperature. However, hydrogen yield is reduced and the carbon monoxide concentration is increased due to the reversed water gas shift reaction. Optimum reactor performance is found using the balance between GHSV-C and GHSV-R. Because of more effective heat transfer characteristics in the vaporizer, it is found that the reactor with combustor arranged as the shell side has better performance compared with the reactor design having the combustor as the tube side under the same operating conditions.

Pd-Ag membrane reactor for steam reforming reactions: a comparison between different fuels

NARCIS (Netherlands)

Gallucci, F.; Basile, A.

2008-01-01

The simulation of a dense Pd-based membrane reactor for carrying out the methane, the methanol and the ethanol steam reforming (SR) reactions for pure hydrogen production is performed. The same simulation is also performed in a traditional reactor. This modelling work shows that the use of membrane

FLUIDIZED BED STEAM REFORMER MONOLITH FORMATION

International Nuclear Information System (INIS)

Jantzen, C

2006-01-01

Fluidized Bed Steam Reforming (FBSR) is being considered as an alternative technology for the immobilization of a wide variety of aqueous high sodium containing radioactive wastes at various DOE facilities in the United States. The addition of clay, charcoal, and a catalyst as co-reactants converts aqueous Low Activity Wastes (LAW) to a granular or ''mineralized'' waste form while converting organic components to CO 2 and steam, and nitrate/nitrite components, if any, to N 2 . The waste form produced is a multiphase mineral assemblage of Na-Al-Si (NAS) feldspathoid minerals with cage-like structures that atomically bond radionuclides like Tc-99 and anions such as SO 4 , I, F, and Cl. The granular product has been shown to be as durable as LAW glass. Shallow land burial requires that the mineralized waste form be able to sustain the weight of soil overburden and potential intrusion by future generations. The strength requirement necessitates binding the granular product into a monolith. FBSR mineral products were formulated into a variety of monoliths including various cements, Ceramicrete, and hydroceramics. All but one of the nine monoliths tested met the 2 durability specification for Na and Re (simulant for Tc-99) when tested using the Product Consistency Test (PCT; ASTM C1285). Of the nine monoliths tested the cements produced with 80-87 wt% FBSR product, the Ceramicrete, and the hydroceramic produced with 83.3 wt% FBSR product, met the compressive strength and durability requirements for an LAW waste form

Numerical simulation of effect of catalyst wire-mesh pressure drop characteristics on flow distribution in catalytic parallel plate steam reformer

DEFF Research Database (Denmark)

Sigurdsson, Haftor Örn; Kær, Søren Knudsen

2012-01-01

Steam reforming of hydrocarbons using a catalytic plate-type-heat-exchanger (CPHE) reformer is an attractive method of producing hydrogen for a fuel cell-based micro combined-heat-and-power system. In this study the flow distribution in a CPHE reformer, which uses a coated wire-mesh catalyst...

A novel and anti-agglomerating Ni@yolk–ZrO₂ structure with sub-10 nm Ni core for high performance steam reforming of methane

OpenAIRE

Lim, Zi-Yian; Wu, Chunzheng; Wang, Wei Guo; Choy, Kwang-Leong; Yin, Hongfeng

2015-01-01

Steam reforming of methane is a versatile technology for hydrogen production in oil refinery and fuel cell applications. Using natural gas is a promising method to produce rich-hydrogen gas. Ni@yolk–ZrO₂ catalyst is used to study steam reforming of methane under various GHSVs, steam-to-carbon (S/C) ratio, and its recyclability. The catalyst was characterized using a combination of XRD, TEM, AAS, TPR, TPH, TGA, BET, XPS, and Raman techniques. The catalyst is evaluated on time stream and identi...

Hydrogen Production via a High-Efficiency Low-Temperature Reformer

Energy Technology Data Exchange (ETDEWEB)

Paul KT Liu; Theo T. Tsotsis

2006-05-31

Fuel cells are promoted by the US government as a viable alternative for clean and efficient energy generation. It is anticipated that the fuel cell market will rise if the key technical barriers can be overcome. One of them is certainly fuel processing and purification. Existing fuel reforming processes are energy intensive, extremely complicated and capital intensive; these disadvantages handicap the scale-down of existing reforming process, targeting distributed or on-board/stationary hydrogen production applications. Our project involves the bench-scale demonstration of a high-efficiency low-temperature steam reforming process. Hydrogen production can be operated at 350 to 400ºC with our invention, as opposed to >800ºC of existing reforming. In addition, our proposed process improves the start-up deficiency of conventional reforming due to its low temperature operation. The objective of this project is to demonstrate the invented process concept via a bench scale unit and verify mathematical simulation for future process optimization study. Under this project, we have performed the experimental work to determine the adsorption isotherm, reaction kinetics, and membrane permeances required to perform the process simulation based upon the mathematical model developed by us. A ceramic membrane coated with palladium thin film fabricated by us was employed in this study. The adsorption isotherm for a selected hydrotalcite adsorbent was determined experimentally. Further, the capacity loss under cyclic adsorption/desorption was confirmed to be negligible. Finally a commercial steam reforming catalyst was used to produce the reaction kinetic parameters required for the proposed operating condition. With these input parameters, a mathematical simulation was performed to predict the performance of the invented process. According to our simulation, our invented hybrid process can deliver 35 to 55% methane conversion, in comparison with the 12 and 18-21% conversion of

Phase 2 THOR Steam Reforming Tests for Sodium Bearing Waste Treatment

Energy Technology Data Exchange (ETDEWEB)

Nicholas R. Soelberg

2004-01-01

About one million gallons of acidic, hazardous, and radioactive sodium-bearing waste is stored in stainless steel tanks at the Idaho Nuclear Technology and Engineering Center (INTEC), which is a major operating facility of the Idaho National Engineering and Environmental Laboratory. Steam reforming is a candidate technology being investigated for converting the waste into a road ready waste form that can be shipped to the Waste Isolation Pilot Plant in New Mexico for interment. A steam reforming technology patented by Studsvik, Inc., and licensed to THOR Treatment Technologies has been tested in two phases using a Department of Energy-owned fluidized bed test system located at the Science Applications International Corporation (SAIC) Science and Technology Applications Research Center located in Idaho Falls, Idaho. The Phase 1 tests were reported earlier in 2003. The Phase 2 tests are reported here. For Phase 2, the process feed rate, stoichiometry, and chemistry were varied to identify and demonstrate process operation and product characteristics under different operating conditions. Two test series were performed. During the first series, the process chemistry was designed to produce a sodium carbonate product. The second series was designed to produce a more leach-resistant, mineralized sodium aluminosilicate product. The tests also demonstrated the performance of a MACT-compliant off-gas system.

Thermodynamic modeling of the power plant based on the SOFC with internal steam reforming of methane

International Nuclear Information System (INIS)

Ivanov, Peter

2007-01-01

Mathematical model based on the thermodynamic modeling of gaseous mixtures is developed for SOFC with internal steam reforming of methane. Macroscopic porous-electrode theory, including non-linear kinetics and gas-phase diffusion, is used to calculate the reforming reaction and the concentration polarization. Provided the data concerning properties and costs of materials the model is fit for wide range of parametric analysis of thermodynamic cycles including SOFC

Methanol steam-reforming in a catalytic fixed bed reactor

Energy Technology Data Exchange (ETDEWEB)

Duesterwald, H G; Hoehlein, B; Kraut, H; Meusinger, J; Peters, R [Research Centre Juelich (KFA) (Germany). Inst. of Energy Process Engineering; Stimming, U [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Festkoerperphysik und Techn. Phys.

1997-12-01

Designing an appropriate methanol steam reformer requires detailed knowledge about the processes within such a reactor. Thus, the axial temperature and concentration gradients and catalyst ageing were investigated. It was found that for a fresh catalyst load, the catalyst located in the reactor entrance was most active during the experiment. The activity of this part of the catalyst bed decreased after some time of operation due to ageing. With further operation, the most active zone moved through the catalyst bed. From the results concerning hydrogen production and catalyst degradation, the necessary amount of catalyst for a mobile PEMFC-system can be estimated. (orig.)

Study on methane separation from steam reforming product gas with polyimide membrane

International Nuclear Information System (INIS)

Koiso, Hiroshi; Inagaki, Yoshiyuki; Aita, Hideki; Sekita, Kenji; Haga, Katsuhiro; Hino, Ryutaro.

1997-10-01

In the HTTR hydrogen production system by steam reforming of natural gas (main component: CH 4 ), CH 4 conversion rate is limited to approximately 65% due to high pressure and low temperature conditions (4.5 MPa, 800degC). The one of the measures to improve CH 4 conversion is recycling of residual CH 4 extracted from steam reforming product gas with a gas separator. Experimental and analytical studies on CH 4 separation from gas mixture composed of CH 4 , H 2 , CO 2 and CO were carried out to investigate gas separation characteristics of a polyimide membrane gas separator. Measured permeability of each gas in gas mixture was reduced from 1/3 to 1/14 of that obtained with a single gas (catalog value). The polyimide membrane could extracted CH 4 of approximately 80% from gas mixture, then, H 2 and CO 2 more than 98% were removed. It was confirmed that the polyimide membrane could be available to residual CH 4 recycling. The analytical results by a difference method gave good prospects of experimental results such as permeated flow rate, mol-fraction profiles and so on. Therefore, it can be said the analysis method was established. (author)

First-principles investigations of the Ni3Sn alloy at steam reforming conditions

DEFF Research Database (Denmark)

Saadi, Souheil; Hinnemann, Berit; Helveg, Stig

2009-01-01

The structure and surface composition of a Ni3Sn alloy at conditions relevant for the steam reforming reaction was investigated using density functional theory calculations. Both the flat Ni3Sn [1 0 (1) over bar 0] surface and a surface with steps in the closed packed direction [1 0 (1) over bar 0...

On the potential of nickel catalysts for steam reforming in membrane reactors

Energy Technology Data Exchange (ETDEWEB)

Pieterse, J.A.Z.; Boon, J.; Van Delft, Y.C.; Dijkstra, J.W.; Van den Brink, R.W. [Energy research Center of the Netherlands, P.O. Box 1, 1755 ZG Petten (Netherlands)

2010-10-15

Hydrogen membrane reactors have been identified as a promising option for hydrogen production for power generation from natural gas with pre-combustion decarbonisation. While Pd or Pd-alloy membranes already provide good hydrogen permeances the most suitable catalyst design for steam reforming in membrane reactors (SRMR) is yet to be identified. This contribution aims to provide insight in the suitability of nickel based catalysts in SRMR. The use of nickel (Ni) catalysts would benefit the cost-effectiveness of membrane reactors and therefore its feasibility. For this, the activity of nickel catalysts in SRMR was assessed with kinetics reported in literature. A 1D model was composed in order to compare the hydrogen production rates derived from the kinetics with the rate of hydrogen withdrawal by permeation. Catalyst stability was studied by exposing the catalysts to reformate gas with two different H/C ratios to mimic the hydrogen lean reformate gas in the membrane reactor. For both the activity (modeling) and stability study the Ni-based catalysts were compared to relevant catalyst compositions based on rhodium (Rh). Using the high pressure kinetics reported for Al2O3 supported Rh and MgAl2O4 and Al2O3 supported Ni catalyst it showed that Ni and Rh catalysts may very well provide similar hydrogen production rates. Interestingly, the stability of Ni-based catalysts proved to be superior to precious metal based catalysts under exposure to simulated reformate feed gas with low H/C molar ratio. A commercial (pre-)reforming Ni-based catalyst was selected for further testing in an experimental membrane reactor for steam reforming at high pressure. During the test period 98% conversion at 873 K could be achieved. The conversion was adjusted to approximately 90% and stable conversion was obtained during the test period of another 3 weeks. Nonetheless, carbon quantification tests of the Ni catalyst indicated that a small amount of carbon had deposited onto the catalyst

FLUIDIZED BED STEAM REFORMER MONOLITH FORMATION

Energy Technology Data Exchange (ETDEWEB)

Jantzen, C

2006-12-22

Fluidized Bed Steam Reforming (FBSR) is being considered as an alternative technology for the immobilization of a wide variety of aqueous high sodium containing radioactive wastes at various DOE facilities in the United States. The addition of clay, charcoal, and a catalyst as co-reactants converts aqueous Low Activity Wastes (LAW) to a granular or ''mineralized'' waste form while converting organic components to CO{sub 2} and steam, and nitrate/nitrite components, if any, to N{sub 2}. The waste form produced is a multiphase mineral assemblage of Na-Al-Si (NAS) feldspathoid minerals with cage-like structures that atomically bond radionuclides like Tc-99 and anions such as SO{sub 4}, I, F, and Cl. The granular product has been shown to be as durable as LAW glass. Shallow land burial requires that the mineralized waste form be able to sustain the weight of soil overburden and potential intrusion by future generations. The strength requirement necessitates binding the granular product into a monolith. FBSR mineral products were formulated into a variety of monoliths including various cements, Ceramicrete, and hydroceramics. All but one of the nine monoliths tested met the <2g/m{sup 2} durability specification for Na and Re (simulant for Tc-99) when tested using the Product Consistency Test (PCT; ASTM C1285). Of the nine monoliths tested the cements produced with 80-87 wt% FBSR product, the Ceramicrete, and the hydroceramic produced with 83.3 wt% FBSR product, met the compressive strength and durability requirements for an LAW waste form.

The role of promoters for Ni catalysts in low temperature (membrane) steam methane reforming

NARCIS (Netherlands)

Ligthart, D.A.J.M.; Pieterse, J.A.Z.; Hensen, E.J.M.

2011-01-01

In the search for active and stable Ni-based catalysts for steam methane reforming in membrane reactors, the effect of three different promoters La, B and Rh was compared. Promoted and unpromoted Ni catalysts were characterized by TEM, TPR and X-ray absorption spectroscopy. The average Ni particle

Structural and surface changes of cobalt modified manganese oxide during activation and ethanol steam reforming reaction

Science.gov (United States)

Gac, Wojciech; Greluk, Magdalena; Słowik, Grzegorz; Turczyniak-Surdacka, Sylwia

2018-05-01

Surface and structural changes of unmodified manganese and cobalt-manganese oxide during activation and ethanol steam reforming reaction conditions (ESR) were studied by means of X-ray diffraction, X-ray photoelectron spectroscopy, temperature-programmed reduction/oxidation (TPR/TPO) and transmission electron microscopy. It was shown that synthesis of cobalt manganese oxide by the redox precipitation method led to the formation of strongly dispersed cobalt ionic species within cryptomelane-based manganese oxide structure. Development of large cube-like MnO nanoparticles with spherical cobalt metallic crystallites decorated by manganese oxide on the high oxidation state and potassium species was observed during reduction. Cobalt manganese catalyst showed high initial activity and selectivity to H2 and CO2 in ethanol stem reforming reaction in the range of 390-480 °C. The drop of ethanol conversion and changes of selectivity with the time-on-stream were observed. An increase of reaction temperature led to intensification of deactivation phenomena. TEM studies evidenced coexistence of Co and CoOx nanoparticles formed under ethanol steam reforming conditions, partially covered by filamentous and encapsulating carbonaceous deposits.

Ni-Based Catalysts for Low Temperature Methane Steam Reforming: Recent Results on Ni-Au and Comparison with Other Bi-Metallic Systems

Directory of Open Access Journals (Sweden)

Anna M. Venezia

2013-06-01

Full Text Available Steam reforming of light hydrocarbons provides a promising method for hydrogen production. Ni-based catalysts are so far the best and the most commonly used catalysts for steam reforming because of their acceptably high activity and significantly lower cost in comparison with alternative precious metal-based catalysts. However, nickel catalysts are susceptible to deactivation from the deposition of carbon, even when operating at steam-to-carbon ratios predicted to be thermodynamically outside of the carbon-forming regime. Reactivity and deactivation by carbon formation can be tuned by modifying Ni surfaces with a second metal, such as Au through alloy formation. In the present review, we summarize the very recent progress in the design, synthesis, and characterization of supported bimetallic Ni-based catalysts for steam reforming. The progress in the modification of Ni with noble metals (such as Au and Ag is discussed in terms of preparation, characterization and pretreatment methods. Moreover, the comparison with the effects of other metals (such as Sn, Cu, Co, Mo, Fe, Gd and B is addressed. The differences of catalytic activity, thermal stability and carbon species between bimetallic and monometallic Ni-based catalysts are also briefly shown.

Application of bench-scale biocalorimetry to photoautotrophic cultures

NARCIS (Netherlands)

Janssen, M.; Patino, R.; Stockar, von U.

2005-01-01

Bench-scale biocalorimetry (=1 L) allows for the determination of the metabolic heat flow during bioprocesses under complete control of all process conditions for extended periods of time. It can be combined with a number of on-line and off-line measurement techniques. This combination can

Kinetic Studies on State of the Art Solid Oxide Cells – A Comparison between Hydrogen/Steam and Reformate Fuels

DEFF Research Database (Denmark)

Njodzefon, Jean-Claude; Graves, Christopher R.; Mogensen, Mogens Bjerg

2015-01-01

Electrochemical reaction kinetics at the electrodes of Solid Oxide Cells (SOCs) were investigated at 700 °C for two cells with different fuel electrode microstructures as well as on a third cell with a reduced active electrode area. Three fuel mixtures were investigated – hydrogen/steam and refor......Electrochemical reaction kinetics at the electrodes of Solid Oxide Cells (SOCs) were investigated at 700 °C for two cells with different fuel electrode microstructures as well as on a third cell with a reduced active electrode area. Three fuel mixtures were investigated – hydrogen....../steam fuel split into two processes with opposing temperature behavior in the reformate fuels. An 87.5% reduction in active electrode area diminishes the gas conversion impedance in the hydrogen/steam fuel at high fuel flow rates. In both reformates, the second and third lowest frequency processes merged...

PREPARATION, CHARACTERIZATION AND CATALYTIC ACTIVITY TEST OF CoMo/ZnO CATALYST ON ETHANOL CONVERSION USING STEAM REFORMING METHOD

Directory of Open Access Journals (Sweden)

Wega Trisunaryanti

2010-06-01

Full Text Available Preparation, characterization and catalytic activity test of CoMo/ZnO catalyst for steam reforming of ethanol have been investigated. The catalysts preparation was carried out by impregnation of Co and/or Mo onto ZnO sample. Water excess was used in ethanol feed for steam reforming process under mol ratio of ethanol:water (1:10. Characterizations of catalysts were conducted by analysis of metal content using Atomic Absorption Spectroscopy (AAS. Determination of catalysts acidity was conducted by gravimetric method of adsorption of pyridine base. Catalytic activity test on ethanol conversion using steam reforming method was conducted in a semi-flow reactor system, at a temperature of 400 oC, for 1.5 h under N2 flow rate of 10 mL/min. Gas product was analyzed by gas chromatograph with TCD system. The results of catalysts characterizations showed that the impregnation of Co and/or Mo metals on ZnO sample increased its acidity and specific surface area. The content of Co in Co/ZnO and CoMo/ZnO catalysts was 1.14 and 0.49 wt%. The Mo content in CoMo/ZnO catalyst was 0.36 wt%. The catalytic activity test result on ethanol conversion showed that the ZnO, Co/ZnO, and CoMo/ZnO catalysts produced gas fraction of 16.73, 28.53, and 35.53 wt%, respectively. The coke production of ZnO, Co/ZnO, and CoMo/ZnO catalysts was 0.86, 0.24, and 0.08 wt%, respectively. The gas products consisted mainly of hydrogen.   Keywords: CoMo/ZnO catalyst, steam reforming, ethanol

Hydrogen Production from Methanol Steam Reforming over TiO2 and CeO2 Pillared Clay Supported Au Catalysts

Directory of Open Access Journals (Sweden)

Rongbin Zhang

2018-01-01

Full Text Available Abstract: Methanol steam reforming is a promising process for the generation of hydrogen. In this study, Au catalysts supported on modified montmorillonite were prepared and their catalytic activity for methanol steam reforming was investigated at 250–500 °C. The physical and chemical properties of the as-prepared catalysts were characterized by Brunauer–Emmet–Teller method (BET, X-ray diffraction (XRD, transmission electron microscopic (TEM, scanning electron microscopy (SEM, X-ray photoelectron spectroscopy (XPS, Inductively Coupled Plasma (ICP, and thermogravimetrc analysis (TGA. For the catalysts examined, Au-Ti-Ce/Na-ABen exhibits the best catalytic performance with methanol conversion of 72% and H2 selectivity of 99% at 350 °C. This could be attributed to Au, Ce, and Ti species which form a solid solution and move into the interlayer space of the bentonite leading to a high surface area, large average pore volume, large average pore diameter, and small Au particle size. We considered that the synergistic effect of the crosslinking agent, the Ce species, and the Au active sites were responsible for the high activity of Au-Ti-Ce/Na-ABen catalyst for methanol steam reforming.

Steam reforming of heptane in a fluidized bed membrane reactor

Science.gov (United States)

Rakib, Mohammad A.; Grace, John R.; Lim, C. Jim; Elnashaie, Said S. E. H.

n-Heptane served as a model compound to study steam reforming of naphtha as an alternative feedstock to natural gas for production of pure hydrogen in a fluidized bed membrane reactor. Selective removal of hydrogen using Pd 77Ag 23 membrane panels shifted the equilibrium-limited reactions to greater conversion of the hydrocarbons and lower yields of methane, an intermediate product. Experiments were conducted with no membranes, with one membrane panel, and with six panels along the height of the reactor to understand the performance improvement due to hydrogen removal in a reactor where catalyst particles were fluidized. Results indicate that a fluidized bed membrane reactor (FBMR) can provide a compact reformer for pure hydrogen production from a liquid hydrocarbon feedstock at moderate temperatures (475-550 °C). Under the experimental conditions investigated, the maximum achieved yield of pure hydrogen was 14.7 moles of pure hydrogen per mole of heptane fed.

Thermochemical recuperative combined cycle with methane-steam reforming combustion; Tennengasu kaishitsu nensho ni yoru konbaindo saikuru hatsuden no kokoritsuka oyobi denryoku fuka heijunka taio

Energy Technology Data Exchange (ETDEWEB)

Kikuchi, R.; Essaki, K.; Tsutsumi, A. [The University of Tokyo, Tokyo (Japan). Dept. of Chemical System Engineering; Kaganoi, S.; Kurimura, H. [Teikoku Sekiyu Co., Tokyo (Japan); Sasaki, T.; Ogawa, T. [Toshiba Co., Tokyo (Japan)

2000-03-10

Thermochemical recuperative combined cycles with methane-steam reforming are proposed for improving their thermal efficiency and for peak-load leveling. For targeting higher thermal efficiency, a cycle with methane-steam reforming reaction heated by gas turbine exhaust was analyzed. The inlet temperature of gas turbine was set at 1,350 degree C. Low-pressure steam extracted from a steam turbine is mixed with methane, and then this mixture is heated by part of the gas turbine exhaust to promote a reforming reaction. The rest of the exhaust heat is used to produce steam, which drives steam turbines to generate electricity. The effect of steam-to-methane ratio (S/C) on thermal efficiency of the cycle, as well as on methane conversion, is investigated by using the ASPEN Plus process simulator. The methane feed rate was fixed at constant and S/C ratio was varied from 2.25 to 4.75. Methane conversion shows an increasing trend toward the ratio and has a maximum value of 17.9 % at S/C=4.0. Thermal efficiency for the system is about 51 % higher than that calculated for a conventional 1,300 degree C class combined cycle under similar conditions. A thermochemical recuperative combined cycle is designed for peak-load leveling. In night-time operation from 20 : 00 to 8 : 00 it stores hydrogen produced by methane steam reforming at S/C=3.9 to save power generation. The gas turbine inlet temperature is 1,330 degree C. In daytime operation from 8 : 00 to 20 : 00 the chemically recuperated combined cycle operated at S/C=2.0 is driven by the mixture of a combined cycle operated at constant load with the same methane feed rate, whereas daytime operation generated power 1.26 times larger than that of the combined cycle. (author)

Experimental and Numerical Study of Low Temperature Methane Steam Reforming for Hydrogen Production

Directory of Open Access Journals (Sweden)

Martin Khzouz

2017-12-01

Full Text Available Low temperature methane steam reforming for hydrogen production, using experimental developed Ni/Al2O3 catalysts is studied both experimentally and numerically. The catalytic activity measurements were performed at a temperature range of 500–700 °C with steam to carbon ratio (S/C of 2 and 3 under atmospheric pressure conditions. A mathematical analysis to evaluate the reaction feasibility at all different conditions that have been applied by using chemical equilibrium with applications (CEA software and in addition, a mathematical model focused on the kinetics and the thermodynamics of the reforming reaction is introduced and applied using a commercial finite element analysis software (COMSOL Multiphysics 5.0. The experimental results were employed to validate the extracted simulation data based on the yields of the produced H2, CO2 and CO at different temperatures. A maximum hydrogen yield of 2.7 mol/mol-CH4 is achieved at 700 °C and S/C of 2 and 3. The stability of the 10%Ni/Al2O3 catalyst shows that the catalyst is prone to deactivation as supported by Thermogravimetric Analysis TGA results.

Cometabolic biotreatment of TCE-contaminated groundwater: Laboratory and bench-scale development studies

International Nuclear Information System (INIS)

Donaldson, T.L.; Jennings, H.L.; Lucero, A.J.; Strandberg, G.W.; Morris, M.I.; Palumbo, A.V.; Boerman, P.A.; Tyndall, R.L.

1992-01-01

The Oak Ridge National Laboratory is conducting a demonstration of two cometabolic technologies for biotreatment of groundwater contaminated with trichloroethylene (TCE) and other organics. Technologies based on methanotrophic (methane-utilizing) and toluene-degrading microorganisms will be compared side-by-side on the same groundwater stream. Laboratory and bench-scale bioreactor studies have been conducted to guide selection of microbial cultures and operating conditions for the field demonstration. This report presents the results of the laboratory and bench-scale studies for the methanotrophic system

Bench-scale treatability studies for simulated incinerator scrubber blowdown containing radioactive cesium and strontium

International Nuclear Information System (INIS)

Coroneos, A.C.; Taylor, P.A.; Arnold, W.D. Jr.; Bostick, D.A.; Perona, J.J.

1994-12-01

The purpose of this report is to document the results of bench-scale testing completed to remove 137 Cs and 90 Sr from the Oak Ridge K-25 Site Toxic Substances Control Act (TSCA) Incinerator blowdown at the K-25 Site Central Neutralization Facility, a wastewater treatment facility designed to remove heavy metals and uranium from various wastewaters. The report presents results of bench-scale testing using chabazite and clinoptilolite zeolites to remove cesium and strontium; using potassium cobalt ferrocyanide (KCCF) to remove cesium; and using strontium chloride coprecipitation, sodium phosphate coprecipitation, and calcium sulfate coprecipitation to remove strontium. Low-range, average-range, and high-range concentration blowdown surrogates were used to complete the bench-scale testing

Bench for mechanical cleaning of circular welded joints

International Nuclear Information System (INIS)

Sklifasovskij, V.M.

1986-01-01

A special bench for weld reinforcement removal and mechanical cleaning of the heat affected zones was designed to provide for a possibility of an ultrasonic testing of welded joints in the course of steam generator section fabrication. The bench comprises a mechanized roller support for fixing and rotating the workpiece; a lap-cutting device for external machining; milling/grinding tractor for internal machining and a delivery table for tractor approach and departure. The bench performance and overall view are presented. The operation succession is described

Cometabolic biotreatment of TCE-contaminated groundwater - Laboratory and bench-scale development studies

Energy Technology Data Exchange (ETDEWEB)

Donaldson, T L; Palumbo, A V; Boerman, P A; Jennings, H L; Lucero, A J; Tyndall, R L; Strandberg, G W; Morris, M I [Oak Ridge National Laboratory, Oak Ridge, TN (United States)

1992-07-01

The Oak Ridge National Laboratory is conducting a demonstration of two cometabolic technologies for biotreatment of groundwater contaminated with trichloroethylene (TCE) and other organics. Technologies based on methanotrophic (methane-utilizing) and toluene-degrading microorganisms will be compared side-by-side on the same groundwater stream. Laboratory and bench-scale bioreactor studies have been conducted to guide selection of microbial cultures and operating conditions for the field demonstration. This report presents the results of the laboratory and bench-scale studies for the methanotrophic system. (author)

Bi-reforming of methane from any source with steam and carbon dioxide exclusively to metgas (CO-2H2) for methanol and hydrocarbon synthesis.

Science.gov (United States)

Olah, George A; Goeppert, Alain; Czaun, Miklos; Prakash, G K Surya

2013-01-16

A catalyst based on nickel oxide on magnesium oxide (NiO/MgO) thermally activated under hydrogen is effective for the bi-reforming with steam and CO(2) (combined steam and dry reforming) of methane as well as natural gas in a tubular flow reactor at elevated pressures (5-30 atm) and temperatures (800-950 °C). By adjusting the CO(2)-to-steam ratio in the gas feed, the H(2)/CO ratio in the produced syn-gas could be easily adjusted in a single step to the desired value of 2 for methanol and hydrocarbon synthesis.

Membrane steam reforming of natural gas for hydrogen production by utilization of medium temperature nuclear reactor

International Nuclear Information System (INIS)

Djati Hoesen Salimy

2010-01-01

The assessment of steam reforming process with membrane reactor for hydrogen production by utilizing of medium temperature nuclear reactor has been carried out. Difference with the conventional process of natural gas steam reforming that operates at high temperature (800-1000°C), the process with membrane reactor operates at lower temperature (~500°C). This condition is possible because the use of perm-selective membrane that separate product simultaneously in reactor, drive the optimum conversion at the lower temperature. Besides that, membrane reactor also acts the role of separation unit, so the plant will be more compact. From the point of nuclear heat utilization, the low temperature of process opens the chance of medium temperature nuclear reactor utilization as heat source. Couple the medium temperature nuclear reactor with the process give the advantage from the point of saving fossil fuel that give direct implication of decreasing green house gas emission. (author)

Methane Steam Reforming over an Ni-YSZ Solid Oxide Fuel Cell Anode in Stack Configuration

DEFF Research Database (Denmark)

Mogensen, David; Grunwaldt, Jan-Dierk; Hendriksen, Peter Vang

2014-01-01

The kinetics of catalytic steam reforming of methane over an Ni-YSZ anode of a solid oxide fuel cell (SOFC) have been investigated with the cell placed in a stack configuration. In order to decrease the degree of conversion, a single cell stack with reduced area was used. Measurements were...

Sustainable hydrogen from bio-oil - Catalytic steam reforming of acetic acid as a model oxygenate

NARCIS (Netherlands)

Takanabe, Kazuhiro; Seshan, K.; Lefferts, Leon; Aika, Ken-ichi

2004-01-01

Steam reforming of acetic acid as a model oxygenate present in bio-oil over Pt/ZrO2 catalysts has been studied. Pt/ZrO2 catalysts are very active, completely converting acetic acid and give hydrogen yield close to thermodynamic equilibrium. The catalyst deactivated by formation of oligomers, which

Computational Investigation of the Thermochemistry and Kinetics of Steam Methane Reforming Over a Multi-Faceted Nickel Catalyst

KAUST Repository

Blaylock, D. Wayne; Zhu, Yi-An; Green, William H.

2011-01-01

A microkinetic model of steam methane reforming over a multi-faceted nickel surface using planewave, periodic boundary condition density functional theory is presented. The multi-faceted model consists of a Ni(111) surface, a Ni(100) surface

Sustainable hydrogen from bio-oil - Catalytic steam reforming of acetic acid as a model oxygenate

NARCIS (Netherlands)

Takanabe, Kazuhiro; Aika, Ken-ichi; Seshan, K.; Lefferts, Leon

Studies were conducted with acetic acid (HAc) as model oxygenate for the design of active and stable catalysts for steam reforming of bio-oil. Pt/ZrO2 catalysts were prepared by wet impregnation technique. The Pt/ZrO2 catalysts showed high activities at initial time on stream, but lost its activity

CO-free hydrogen production by ethanol steam reforming in a Pd-Ag membrane reactor

NARCIS (Netherlands)

Basile, A.; Gallucci, F.; Iulianelli, A.; Tosti, S.

2008-01-01

In this work, the ethanol steam reforming (ESR) reaction has been studied by using a dense Pd-Ag membrane reactor (MR) by varying the water/ethanol molar ratio between 3:1 and 9:1 in a temperature range of 300-400°C and at 1.3 bar as reaction pressure. The MR was packed with a commercial Ru-based

Energy efficiency of a direct-injection internal combustion engine with high-pressure methanol steam reforming

International Nuclear Information System (INIS)

Poran, Arnon; Tartakovsky, Leonid

2015-01-01

This article discusses the concept of a direct-injection ICE (internal combustion engine) with thermo-chemical recuperation realized through SRM (steam reforming of methanol). It is shown that the energy required to compress the reformate gas prior to its injection into the cylinder is substantial and has to be accounted for. Results of the analysis prove that the method of reformate direct-injection is unviable when the reforming is carried-out under atmospheric pressure. To reduce the energy penalty resulted from the gas compression, it is suggested to implement a high-pressure reforming process. Effects of the injection timing and the injector's flow area on the ICE-SRM system's fuel conversion efficiency are studied. The significance of cooling the reforming products prior to their injection into the engine-cylinder is demonstrated. We show that a direct-injection ICE with high-pressure SRM is feasible and provides a potential for significant efficiency improvement. Development of injectors with greater flow area shall contribute to further efficiency improvements. - Highlights: • Energy needed to compress the reformate is substantial and has to be accounted for. • Reformate direct-injection is unviable if reforming is done at atmospheric pressure. • Direct-injection engine with high-pressure methanol reforming is feasible. • Efficiency improvement by 12–14% compared with a gasoline-fed engine was shown

Steam reforming of cyclic model compounds of bio-oil over Ni-based catalysts: Product distribution and carbon formation

DEFF Research Database (Denmark)

Trane-Restrup, Rasmus; Jensen, Anker Degn

2015-01-01

Steam reforming (SR) and oxidative steam reforming (OSR) of furfural, 2-methylfuran, and guaiacol have been investigated in the temperature range 400-800°C at a steam to carbon (S/C)-ratio of 5 and oxygen to carbon (O/C)-ratio of 0.2-1.4 over Ni/CeO2-K/MgAl2O4. Carbon oxides and H2 were the major...... products in the SR of 2-methylfuran and furfural, while the by-products were methane, ethanol, 2-propanol, and acetone. Temperatures of 500°C or above were needed to minimize the formation of by-products in the SR of 2-methylfuran and furfural. Phenolics, like benzenediols and phenol, were produced in high...... yields in the SR of guaiacol and temperatures of 780°C were needed to totally convert guaiacol to carbon oxides and H2.Carbon deposition was observed in the SR of all three model compounds and was most severe for guaiacol followed by furfural and 2-methylfuran. The carbon deposition could be reduced...

Dynamic performance investigation of once-through-type steam generator for NPP using a large-scale model

International Nuclear Information System (INIS)

Kats, F.M.; Ostrovskij, L.A.; Ehskin, N.B.

1985-01-01

An experimental bench is described as well as the results of dynamic performance investigation of mass- and heat transfer of the once-through type steam generator for the NPP with weak superheat. Coolant for the primary and secondary circuit is water. Under investigation conditions the possibility of changin.o primary and secondary circuit temperatures has been supphed as well as the primary circuit flow rate and the secondary circuit pressure changes. Transients for differen.t operating conditions are considered. The possibility for construction of the steam generator automatic control system is based

Uncertainty Quantification Analysis of Both Experimental and CFD Simulation Data of a Bench-scale Fluidized Bed Gasifier

Energy Technology Data Exchange (ETDEWEB)

Shahnam, Mehrdad [National Energy Technology Lab. (NETL), Morgantown, WV (United States). Research and Innovation Center, Energy Conversion Engineering Directorate; Gel, Aytekin [ALPEMI Consulting, LLC, Phoeniz, AZ (United States); Subramaniyan, Arun K. [GE Global Research Center, Niskayuna, NY (United States); Musser, Jordan [National Energy Technology Lab. (NETL), Morgantown, WV (United States). Research and Innovation Center, Energy Conversion Engineering Directorate; Dietiker, Jean-Francois [West Virginia Univ. Research Corporation, Morgantown, WV (United States)

2017-10-02

Adequate assessment of the uncertainties in modeling and simulation is becoming an integral part of the simulation based engineering design. The goal of this study is to demonstrate the application of non-intrusive Bayesian uncertainty quantification (UQ) methodology in multiphase (gas-solid) flows with experimental and simulation data, as part of our research efforts to determine the most suited approach for UQ of a bench scale fluidized bed gasifier. UQ analysis was first performed on the available experimental data. Global sensitivity analysis performed as part of the UQ analysis shows that among the three operating factors, steam to oxygen ratio has the most influence on syngas composition in the bench-scale gasifier experiments. An analysis for forward propagation of uncertainties was performed and results show that an increase in steam to oxygen ratio leads to an increase in H2 mole fraction and a decrease in CO mole fraction. These findings are in agreement with the ANOVA analysis performed in the reference experimental study. Another contribution in addition to the UQ analysis is the optimization-based approach to guide to identify next best set of additional experimental samples, should the possibility arise for additional experiments. Hence, the surrogate models constructed as part of the UQ analysis is employed to improve the information gain and make incremental recommendation, should the possibility to add more experiments arise. In the second step, series of simulations were carried out with the open-source computational fluid dynamics software MFiX to reproduce the experimental conditions, where three operating factors, i.e., coal flow rate, coal particle diameter, and steam-to-oxygen ratio, were systematically varied to understand their effect on the syngas composition. Bayesian UQ analysis was performed on the numerical results. As part of Bayesian UQ analysis, a global sensitivity analysis was performed based on the simulation results, which shows

Process for manufacture of a catalyst suitable for the steam reforming of hydrocarbons and for obtaining methane

Energy Technology Data Exchange (ETDEWEB)

Golebiowski, A.; Romotowski, T.; Hennel, W.; Wroblewska-Wroblewska, T.; Polanski, A.; Janecki, Z.; Paluch-Paluch, S.

1982-07-29

The invention concerns a process for the manufacture of a catalyst suitable for the steam reforming of hydrocarbons or for obtaining methane, by the deposition of the catalytic components on a metal carrier with a large surface area, particularly a process for the manufacture of a solid nickel catalyst, which is suitable for the steam reforming of hydrocarbons, particularly of methane. The following steps of the process are carried out: producing a highly porous layer of spongy metal from Ni powder on the side of a metal wall away from a heat medium, which separates the reaction mixture from the heat medium, then separate application of a non-reducing oxide (Al/sub 2/O/sub 3/) and a reducing oxide (nickel oxide) on the spongy metal by soaking with metal salt solution and then roasting in the temperature range of 400 to 1200/sup 0/C.

Steam reforming of ethanol over Ni-based catalysts: Effect of feed composition on catalyst stability

DEFF Research Database (Denmark)

Trane-Restrup, Rasmus; Dahl, Søren; Jensen, Anker Degn

2014-01-01

In this work the effects of steam-to-carbon ratio (S/C), and addition of H2 or O2 to the feed on the product yields and carbon deposition in the steam reforming (SR) of ethanol over Ni/MgAl2O4, Ni/Ce0.6Zr0.4O2, and Ni/CeO2 at 600 °C have been investigated. Increasing the S/C-ratio from 1.6 to 8.3...... showed stable behavior and an average rate of carbon deposition of less than 7 μg C/gCat h. The results indicate that stable operation of ethanol SR is only possible under oxidative conditions....

Life cycle inventory analysis of hydrogen production by the steam-reforming process: comparison between vegetable oils and fossil fuels as feedstock

International Nuclear Information System (INIS)

Marquevich, M.; Sonnemann, G.W.; Castells, F.; Montane, D.

2002-01-01

A life cycle inventory analysis has been conducted to assess the environmental load, specifically CO 2 (fossil) emissions and global warming potential (GWP), associated to the production of hydrogen by the steam reforming of hydrocarbon feedstocks (methane and naphtha) and vegetable oils (rapeseed oil, soybean oil and palm oil). Results show that the GWPs associated with the production of hydrogen by steam reforming in a 100 years time frame are 9.71 and 9.46 kg CO 2 -equivalent/kg H 2 for natural gas and naphtha, respectively. For vegetable oils, the GWP decreases to 6.42 kg CO 2 -equivalent/kg H 2 for rapeseed oil, 4.32 for palm oil and 3.30 for soybean oil. A dominance analysis determined that the part of the process that has the largest effect on the GWP is the steam reforming reaction itself for the fossil fuel-based systems, which accounts for 56.7% and 74% of the total GWP for natural gas and naphtha, respectively. This contribution is zero for vegetable oil-based systems, for which harvesting and oil production are the main sources of CO 2 -eq emissions.(author)

Heat supply analysis of steam reforming hydrogen production process in conventional and nuclear

International Nuclear Information System (INIS)

Siti Alimah; Djati Hoesen Salimy

2015-01-01

Tile analysis of heat energy supply in the production of hydrogen by natural gas steam reforming process has been done. The aim of the study is to compare the energy supply system of conventional and nuclear heat. Methodology used in this study is an assessment of literature and analysis based on the comparisons. The study shows that the heat sources of fossil fuels (natural gas) is able to provide optimum operating conditions of temperature and pressure of 850-900 °C and 2-3 MPa, as well as the heat transfer is dominated by radiation heat transfer, so that the heat flux that can be achieved on the catalyst tube relatively high (50-80 kW/m"2) and provide high thermal efficiency of about 85 %. While in the system with nuclear energy, due to the demands of safety, process operating at less than optimum conditions of temperature and pressure of 800-850 °C and 4.5 MPa, as well as the heat transfer is dominated by convection heat transfer, so that the heat flux that can be achieved catalyst tube is relatively low (1020 kW/m"2) and it provides a low thermal efficiency of about 50 %. Modifications of reformer and heat utilization can increase the heat flux up to 40 kW/m"2 so that the thermal efficiency can reach 78 %. Nevertheless, the application of nuclear energy to hydrogen production with steam reforming process is able to reduce the burning of fossil fuels which has implications for the potential decrease in the rate of CO2 emissions into the environment. (author)

Preparation of Cu-Fe-Al-O nanosheets and their catalytic application in methanol steam reforming for hydrogen production

Science.gov (United States)

Wang, Leilei; Zhang, Fan; Miao, Dinghao; Zhang, Lei; Ren, Tiezhen; Hui, Xidong; He, Zhanbing

2017-03-01

Candidates of precious metal catalysts, prepared in a facile and environmental way and showing high catalytic performances at low temperatures, are always highly desired by industry. In this work, large-scale Cu-Fe-Al-O nanosheets were synthesized by facile dealloying of Al-Cu-Fe alloys in NaOH solution. The composition, microscopic morphology, and crystal structure were respectively investigated using wavelength-dispersive x-ray spectroscopy with an electron probe microanalyzer, scanning electron microscopy, x-ray diffraction, and transmission electron microscopy. Furthermore, we found that the 2D Cu-Fe-Al-O nanosheets gave excellent catalytic performances in hydrogen production by methanol steam reforming at relatively low temperatures, e.g. 513 K.

Co-current and counter-current configurations for ethanol steam reforming in a dense Pd-Ag membrane reactor

NARCIS (Netherlands)

Gallucci, F.; de Falco, M.; Tosti, S.; Marrelli, L; Basile, A.

2008-01-01

The ethanol steam-reforming reaction to produce pure hydrogen has been studied theoretically. A mathematical model has been formulated for a traditional system and a palladium membrane reactor packed with a Co-based catalyst and the simulation results related to the membrane reactor for both

Dimensional analysis of small-scale steam explosion experiments

International Nuclear Information System (INIS)

Huh, K.; Corradini, M.L.

1986-01-01

Dimensional analysis applied to Nelson's small-scale steam explosion experiments to determine the qualitative effect of each relevant parameter for triggering a steam explosion. According to experimental results, the liquid entrapment model seems to be a consistent explanation for the steam explosion triggering mechanism. The three-dimensional oscillatory wave motion of the vapor/liquid interface is analyzed to determine the necessary conditions for local condensation and production of a coolant microjet to be entrapped in fuel. It is proposed that different contact modes between fuel and coolant may involve different initiation mechanisms of steam explosions

Dynamic simulation of pure hydrogen production via ethanol steam reforming in a catalytic membrane reactor

International Nuclear Information System (INIS)

Hedayati, Ali; Le Corre, Olivier; Lacarrière, Bruno; Llorca, Jordi

2016-01-01

Ethanol steam reforming (ESR) was performed over Pd-Rh/CeO 2 catalyst in a catalytic membrane reactor (CMR) as a reformer unit for production of fuel cell grade pure hydrogen. Experiments were performed at 923 K, 6–10 bar, and fuel flow rates of 50–200 μl/min using a mixture of ethanol and distilled water with steam to carbon ratio of 3. A static model for the catalytic zone was derived from the Arrhenius law to calculate the total molar production rates of ESR products, i.e. CO, CO 2 , CH 4 , H 2 , and H 2 O in the catalytic zone of the CMR (coefficient of determination R 2  = 0.993). The pure hydrogen production rate at steady state conditions was modeled by means of a static model based on the Sieverts' law. Finally, a dynamic model was developed under ideal gas law assumptions to simulate the dynamics of pure hydrogen production rate in the case of the fuel flow rate or the operating pressure set point adjustment (transient state) at isothermal conditions. The simulation of fuel flow rate change dynamics was more essential compared to the pressure change one, as the system responded much faster to such an adjustment. The results of the dynamic simulation fitted very well to the experimental values at P = 7–10 bar, which proved the robustness of the simulation based on the Sieverts' law. The simulation presented in this work is similar to the hydrogen flow rate adjustments needed to set the electrical load of a fuel cell, when fed online by the pure hydrogen generating reformer studied. - Highlights: • Ethanol steam reforming (ESR) experiments were performed in a Pd-Ag membrane reactor. • The model of the catalytic zone of the reactor was derived from the Arrhenius law. • The permeation zone (membrane) was modeled based on the Sieverts' law. • The Sieverts' law model showed good results for the range of P = 7–10 bar. • Pressure and fuel flow rate adjustments were considered for dynamic simulation.

DEGRADATION OF POLYNUCLEAR AROMATIC HYDROCARBONS UNDER BENCH-SCALE COMPOST CONDITIONS

Science.gov (United States)

The relationship between biomass growth and degradation of polynuclear aromatic hydrocarbons (PAHs) in soil, and subsequent toxicity reduction, was evaluated in 10 in-vessel, bench-scale compost units. Field soil was aquired from the Reilly Tar and Chemical Company Superfund site...

Treatment of Synthetic Wastewater Containing AB14 Pigment by Electrooxidation in both Pilot and Bench Scale Reactors

Directory of Open Access Journals (Sweden)

Jalal Basiri parsa

2016-01-01

Full Text Available The electrochemical oxidation process was used for the degradation of Acid Brown 14 in both bench and pilot scale reactors. The bench scale one with a working volume of 0.5 L was equipped with platinum plate used as the anode and stainless steel (SS-304 plates as the cathode. The pilot scale reactor had a volume of 9 L and was equipped with SS-304 plates used as both the anode and the cathode. Experiments were run using these reactors to investigate the two parameters of energy consumption and anode efficiency. The bench scale reactor was capable of removing 92% and 36% of the dye and COD, respectively, after 18 min of operation. The pilot scale reactor, however, was capable of removing 87% and 59% of the dye and the COD content, respectively, after 60 min of operation. The kinetic study of both the bench and pilot reactors for dye and COD removals showed that both processes followed a zero order kinetic.

Modeling and simulation of a packed bed reactor for hydrogen by methanol steam reforming

International Nuclear Information System (INIS)

Aboudheir, A.; Idem, R.

2004-01-01

'Full text:' The performance of a catalytic packed bed tubular reactor for hydrogen production depends on mass transport characteristics and temperature distribution in the reactor. To accurately predict this performance, a rigorous numerical model has been developed based on coupled mass, energy, and momentum balance equations in cylindrical coordinates. This comprehensive model takes into account the variations of the concentration and temperature in both the axial and radial directions as well as the pressure drop along the packed reactor. Also, experimental measurements for hydrogen production were collected using a manganese-promoted co-precipitated Cu-Al catalyst for methanol-steam reforming in a micro-reactor having 10 mm i.d. and 460 mm overall length. The operating temperature ranged from 443 to 523 K and the space-time ranged from 0.1 to 2.5 kg cat h/kmol CH3OH. The simulation results were found to be in close agreement with the experimental data over the various operating conditions. This confirms the validity of both the numerical model of this work and our previous published kinetics models for this reaction system. In addition, the model formulation is applicable to handle reactions, not only for the microreactor presented in this work, but also, for other laboratory size and industrial scale processes for hydrogen production by hydrocarbon reformation. (author)

Chemical looping reforming in packed-bed reactors : modelling, experimental validation and large-scale reactor design

NARCIS (Netherlands)

Spallina, V.; Marinello, B.; Gallucci, F.; Romano, M.C.; van Sint Annaland, M.

This paper addresses the experimental demonstration and model validation of chemical looping reforming in dynamically operated packed-bed reactors for the production of H2 or CH3OH with integrated CO2 capture. This process is a combination of auto-thermal and steam methane reforming and is carried

Bench-scale magnetic separation of Department of Energy wastes

International Nuclear Information System (INIS)

Hoegler, J.M.

1987-07-01

Criteria were developed for selection of candidate wastes for testing magnetic separation of uranium and/or other paramagnetic materials. A survey of Department of Energy (DOE) hazardous wastes was conducted to determine good candidates for bench-scale magnetic separation tests. Representatives of 21 DOE sites were contacted, and 11 materials were identified as potential candidates for magnetic separation. To date, seven samples have been obtained and tested for separability of uranium with a bench-scale magnetic assaying device. The samples tested have been obtained from the K-1401B and K-1401C ponds in Oak Ridge, Tennessee; from waste piles in Maywood, New Jersey; from North and South Ponds in Richland, Washington; and from magnesium fluoride drums in Fernald, Ohio. The magnetic device utilized in these tests can be used in an open-gradient mode with dry particulate or liquid-suspended materials. Uranium separation from magnesium fluoride has shown exceptionally good performance in both open- and high-gradient modes and could be an important application of the technology

Design and optimization of a fixed - bed reactor for hydrogen production via bio-ethanol steam reforming

International Nuclear Information System (INIS)

Maria A Goula; Olga A Bereketidou; Costas G Economopoulos; Olga A Bereketidou; Costas G Economopoulos

2006-01-01

Global climate changes caused by CO 2 emissions are currently debated around the world. Renewable sources of energy are being sought as alternatives to replace fossil fuels. Hydrogen is theoretically the best fuel, environmentally friendly and its combustion reaction leads only to the production of water. Bio-ethanol has been proven to be effective in the production of hydrogen via steam reforming reaction. In this research the steam reforming reaction of bio-ethanol is studied at low temperatures over 15,3 % Ni/La 2 O 3 catalyst. The reaction and kinetic analysis takes place in a fixed - bed reactor in 130 - 250 C in atmospheric pressure. This study lays emphasis on the design and the optimization of the fixed - bed reactor, including the total volume of the reactor, the number and length of the tubes and the degree of ethanol conversion. Finally, it is represented an approach of the total cost of the reactor, according to the design characteristics and the materials that can be used for its construction. (authors)

Steam reforming of ethanol over Co3O4–Fe2O3 mixed oxides

KAUST Repository

Abdelkader, A.

2013-05-03

Co3O4, Fe2O3 and a mixture of the two oxides Co-Fe (molar ratio of Co3O4/Fe 2O3 = 0.67 and atomic ratio of Co/Fe = 1) were prepared by the calcination of cobalt oxalate and/or iron oxalate salts at 500 C for 2 h in static air using water as a solvent/dispersing agent. The catalysts were studied in the steam reforming of ethanol to investigate the effect of the partial substitution of Co3O4 with Fe2O 3 on the catalytic behaviour. The reforming activity over Fe 2O3, while initially high, underwent fast deactivation. In comparison, over the Co-Fe catalyst both the H2 yield and stability were higher than that found over the pure Co3O4 or Fe 2O3 catalysts. DRIFTS-MS studies under the reaction feed highlighted that the Co-Fe catalyst had increased amounts of adsorbed OH/water; similar to Fe2O3. Increasing the amount of reactive species (water/OH species) adsorbed on the Co-Fe catalyst surface is proposed to facilitate the steam reforming reaction rather than decomposition reactions reducing by-product formation and providing a higher H2 yield. © Copyright © 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

Experience gained in bench scale and pilot scale fluidised bed processing

CSIR Research Space (South Africa)

Hadley, TD

2005-01-01

Full Text Available of titanium dioxide. Expertise in the design and commissioning of industrial-scale plants has led to the supply (through licensees) of a biomass sludge incinerator/boiler generating 26t/h steam, a 20 MW high-sulphur pitch incinerator and a 12 MW fluidised bed...

Thermodynamic analyses of hydrogen production from sub-quality natural gas. Part II: Steam reforming and autothermal steam reforming

Science.gov (United States)

Huang, Cunping; T-Raissi, Ali

Part I of this paper analyzed sub-quality natural gas (SQNG) pyrolysis and autothermal pyrolysis. Production of hydrogen via direct thermolysis of SQNGs produces only 2 mol of hydrogen and 1 mol of carbon per mole of methane (CH 4). Steam reforming of SQNG (SRSQNG) could become a more effective approach because the processes produce two more moles of hydrogen via water splitting. A Gibbs reactor unit operation in the AspenPlus™ chemical process simulator was employed to accomplish equilibrium calculations for the SQNG + H 2O and SQNG + H 2O + O 2 systems. The results indicate that water and oxygen inlet flow rates do not significantly affect the decomposition of hydrogen sulfide (H 2S) at temperatures lower than 1000 °C. The major co-product of the processes is carbonyl sulfide (COS) while sulfur dimer (S 2) and carbon disulfide (CS 2) are minor by-products within this temperature range. At higher temperatures (>1300 °C), CS 2 and S 2 become major co-products. No sulfur dioxide (SO 2) or sulfur trioxide (SO 3) is formed during either SRSQNG or autothermal SRSQNG processes, indicating that no environmentally harmful acidic gases are generated.

Remarkable support effect on the reactivity of Pt/In2O3/MOx catalysts for methanol steam reforming

Science.gov (United States)

Liu, Xin; Men, Yong; Wang, Jinguo; He, Rong; Wang, Yuanqiang

2017-10-01

Effects of supports over Pt/In2O3/MOx catalysts with extremely low loading of Pt (1 wt%) and In2O3 loadings (3 wt%) are investigated for the hydrogen production of methanol steam reforming (MSR) in the temperature range of 250-400 °C. Under practical conditions without the pre-reduction, the 1Pt/3In2O3/CeO2 catalyst shows the highly efficient catalytic performance, achieving almost complete methanol conversion (98.7%) and very low CO selectivity of 2.6% at 325 °C. The supported Pt/In2O3 catalysts are characterized by means of Brunauer-Emmett-Teller (BET) surface area, X-ray diffraction (XRD), high-resolution transmission microscopy (HRTEM), temperature programmed reduction with hydrogen (H2-TPR), CO pulse chemisorption, temperature programmed desorption of methanol and water (CH3OH-TPD and H2O-TPD). These demonstrate that the nature of catalyst support of Pt/In2O3/MOx plays crucial roles in the Pt dispersion associated by the strong interaction among Pt, In2O3 and supporting materials and the surface redox properties at low temperature, and thus affects their capability to activate the reactants and determines the catalytic activity of methanol steam reforming. The superior 1Pt/3In2O3/CeO2 catalyst, exhibiting a remarkable reactivity and stability for 32 h on stream, demonstrates its potential for efficient hydrogen production of methanol steam reforming in mobile and de-centralized H2-fueled PEMFC systems.

Energy Analysis in Combined Reforming of Propane

Directory of Open Access Journals (Sweden)

K. Moon

2013-01-01

Full Text Available Combined (steam and CO2 reforming is one of the methods to produce syngas for different applications. An energy requirement analysis of steam reforming to dry reforming with intermediate steps of steam reduction and equivalent CO2 addition to the feed fuel for syngas generation has been done to identify condition for optimum process operation. Thermodynamic equilibrium data for combined reforming was generated for temperature range of 400–1000°C at 1 bar pressure and combined oxidant (CO2 + H2O stream to propane (fuel ratio of 3, 6, and 9 by employing the Gibbs free energy minimization algorithm of HSC Chemistry software 5.1. Total energy requirement including preheating and reaction enthalpy calculations were done using the equilibrium product composition. Carbon and methane formation was significantly reduced in combined reforming than pure dry reforming, while the energy requirements were lower than pure steam reforming. Temperatures of minimum energy requirement were found in the data analysis of combined reforming which were optimum for the process.

H_2 production by the steam reforming of excess boil off gas on LNG vessels

International Nuclear Information System (INIS)

Fernández, Ignacio Arias; Gómez, Manuel Romero; Gómez, Javier Romero; López-González, Luis M.

2017-01-01

Highlights: • BOG excess in LNG vessels is burned in the GCU without energy use. • The gas management plants need to be improved to increase efficiency. • BOG excess in LNG vessels is used for H_2 production by steam reforming. • The availability of different fuels increases the versatility of the ship. - Abstract: The gas management system onboard LNG (Liquid Natural Gas) vessels is crucial, since the exploitation of the BOG (Boil Off Gas) produced is of utmost importance for the overall efficiency of the plant. At present, LNG ships with no reliquefaction plant consume the BOG generated in the engines, and the excess is burned in the GCU (Gas Combustion Unit) without any energy use. The need to improve the gas management system, therefore, is evident. This paper proposes hydrogen production through a steam reforming plant, using the excess BOG as raw material and thus avoiding it being burned in the GCU. To test the feasibility of integrating the plant, an actual study of the gas management process on an LNG vessel with 4SDF (4 Stroke Dual Fuel) propulsion and with no reliquefaction plant was conducted, along with a thermodynamic simulation of the reforming plant. With the proposed gas management system, the vessel disposes of different fuels, including H_2, a clean fuel with zero ozone-depleting emissions. The availability of H_2 on board in areas with strict anti-pollution regulations, such as ECAs (Emission Control Area), means that the vessel may be navigated without using fossil fuels which generate CO_2 and SO_X emissions. Moreover, while at port, Cold Ironing is avoided, which entails high costs. Thus it is demonstrated that the installation of a reforming plant is both energetically viable and provides greater versatility to the ship.

Steam jet ejectors are examined automatically

International Nuclear Information System (INIS)

Lardiere, C.

2013-01-01

Steam jet ejectors are used in the nuclear industry particularly for the transfer of radioactive fluids. Their working is based on the Venturi effect and the conservation of energy. A steam ejector can be considered as a thermodynamical pump without mobile parts. The Descote enterprise manufactures a broad range of steam jet ejectors and the characterization and testing of the steam ejectors was made manually and empirically so far. A new test bench has been designed, the tests are led automatically and allow a more accurate characterization and optimization of the steam jet ejectors. (A.C.)

A contribution to the modelling of steam reformers for natural gas fuelled fuel cell heating systems; Ein Beitrag zur Modellierung von Dampfreformern fuer erdgasbetriebene Brennstoffzellenheizgeraete

Energy Technology Data Exchange (ETDEWEB)

Nietzsche, Joerg

2010-10-29

The author attempted to verify the assumptions and simplifications of common mathematical models of small-scale steam reformers. The emphasis was on the derivation of important model parameters on the basis of easily identifiable catalyst, fluid and reactor characteristics. An easily validated 2D model of a reformer tube is then used for a wide sensitivity analysis and a comparative investigation of various reactor types. [German] Die Motivation dieser Arbeit liegt in der Ueberpruefung der bislang in mathematischen Modellen von kleintechnischen Dampfreformern getroffenen Annahmen und Vereinfachungen, mit speziellem Augenmerk auf die Aufklaerung der Herkunft wichtiger Modellparameter anhand von leicht bestimmbaren Katalysator-, Fluid- und Reaktoreigenschaften. Ein leicht zu validierendes, zweidimensionales Modell eines Reformerrohres soll im Anschluss fuer eine breit angelegte Sensitivitaetsanalyse und eine vergleichende Untersuchung verschiedener Reaktortypen dienen.

Study of Catalyst Variation Effect in Glycerol Conversion Process to Hydrogen Gas by Steam Reforming

Science.gov (United States)

Widayat; Hartono, R.; Elizabeth, E.; Annisa, A. N.

2018-04-01

Along with the economic development, needs of energy being increase too. Hydrogen as alternative energy has many usages. Besides that, hydrogen is one source of energy that is a clean fuel, but process production of hydrogen from natural gas as a raw material has been used for a long time. Therefore, there is need new invention to produce hydrogen from the others raw material. Glycerol, a byproduct of biodiesel production, is a compound which can be used as a raw material for hydrogen production. By using glycerol as a raw material of hydrogen production, we can get added value of glycerol as well as an energy source solution. The process production of hydrogen by steam reforming is a thermochemical process with efficiency 70%. This process needs contribution of catalyst to improve its efficiency and selectivity of the process. In this study will be examined the effect variation of catalyst for glycerol conversion process to hydrogen by steam reforming. The method for catalyst preparation was variation of catalyst impregnation composition, catalyst calcined with difference concentration of hydrochloric acid and calcined with difference hydrochloric acid ratio. After that, all of catalyst which have been prepared, used for steam reforming process for hydrogen production from glycerol as a raw material. From the study, the highest yield of hydrogen gas showed in the process production by natural zeolite catalyst with 1:15 Hydrochloric acid ratio was 42.28%. Hydrogen yield for 2M calcined natural zeolite catalyst was 38.37%, for ZSM-5 catalyst was 15.83%, for 0.5M calcined natural zeolite was 13.09% and for ultrasonic natural zeolite was 11.43%. The lowest yield of hydrogen gas showed in catalyst 2Zn/ZSM-5 with 11.22%. This result showed that hydrogen yield product was affected by catalyst variation because of the catalyst has difference characteristic and difference catalytic activity after the catalyst preparation process.

In silico search for novel methane steam reforming catalysts

International Nuclear Information System (INIS)

Xu, Yue; Lausche, Adam C; Khan, Tuhin S; Abild-Pedersen, Frank; Studt, Felix; Nørskov, Jens K; Bligaard, Thomas; Wang, Shengguang

2013-01-01

This paper demonstrates a method for screening transition metal and metal alloy catalysts based on their predicted rates and stabilities for a given catalytic reaction. This method involves combining reaction and activation energies (available to the public via a web-based application ‘CatApp’) with a microkinetic modeling technique to predict the rates and selectivities of a prospective material. This paper illustrates this screening technique using the steam reforming of methane to carbon monoxide and hydrogen as a test reaction. While catalysts are already commercially available for this process, the method demonstrated in this paper is very general and could be applied to a wide range of catalytic reactions. Following the steps outlined herein, such an analysis could potentially enable researchers to understand reaction mechanisms on a fundamental level and, on this basis, develop leads for new metal alloy catalysts. (paper)

PRODUCTION OF HYDROGEN FROM THE STEAM AND OXIDATIVE REFORMING OF LPG: THERMODYNAMIC AND EXPERIMENTAL STUDY

Directory of Open Access Journals (Sweden)

P. P. Silva

2015-09-01

Full Text Available AbstractThe objective of this paper was to use a thermodynamic analysis to find operational conditions that favor the production of hydrogen from steam and oxidative reforming of liquefied petroleum gas (LPG. We also analyzed the performance of a catalyst precursor, LaNiO3, in order to compare the performance of the obtained catalyst with the thermodynamic equilibrium predictions. The results showed that it is possible to produce high concentrations of hydrogen from LPG reforming. The gradual increase of temperature and the use of high water concentrations decrease the production of coke and increase the formation of H2. The reaction of oxidative reforming of LPG was more suitable for the production of hydrogen and lower coke formation. Furthermore the use of an excess of water (H2O/LPG =7.0 and intermediate temperatures (973 K are the most suitable conditions for the process.

Analytical study on carbon dioxide reforming of natural gas

International Nuclear Information System (INIS)

Ohashi, Hirofumi; Sakaki, Akihiro; Inagaki, Yoshiyuki

2001-01-01

In recent years, considerable attention has been paid to carbon dioxide reforming of natural gas, namely CO 2 reforming, since it can produce synthesis gas with low hydrogen-to-carbon ratio preferentially used for production of liquid hydrocarbons in the Fischer-Tropsch and methanol syntheses. This reaction has also very important environmental implications because CO 2 , a green house gas, may be converted into valuable feedstock. In JAERI, CO 2 reforming using the out-of-pile test facility, which is a 1/30 scale model of the HTTR hydrogen production system, is also being considered as an application of steam reforming. For the purpose to estimate the reformer performance in the facility, numerical analysis of natural gas reforming processes of CO 2 and combined reactions with steam and CO 2 has been carried out using mathematical model on heat and mass balance accompanied by chemical reactions. The reformer performance was evaluated in the effect of pressure, temperature, process gas composition and reaction rate constants of the catalyst on conversion, product gas composition and heat consumption of He gas. And also, the potential of carbon formation by CH 4 cracking reaction and Boudouard reaction was estimated. (author)

HIGHTEX: a computer program for the steady-state simulation of steam-methane reformers used in a nuclear process heat plant

International Nuclear Information System (INIS)

Tadokoro, Yoshihiro; Seya, Toko

1977-08-01

This report describes a computational model and the input procedure of HIGHTEX, a computer program for steady-state simulation of the steam-methane reformers used in a nuclear process heat plant. The HIGHTEX program simulates rapidly a single reformer tube, and treats the reactant single-phase in the two-dimensional catalyst bed. Output of the computer program is radial distributions of temperature and reaction products in the catalyst-packed bed, pressure loss of the packed bed, stress in the reformer tube, hydrogen permeation rate through the reformer tube, heat rate of reaction, and heat-transfer rate between helium and process gas. The running time (cpu) for a 9m-long bayonet type reformer tube is 12 min with FACOM-230/75. (auth.)

Template-Assisted Wet-Combustion Synthesis of Fibrous Nickel-Based Catalyst for Carbon Dioxide Methanation and Methane Steam Reforming.

Science.gov (United States)

Aghayan, M; Potemkin, D I; Rubio-Marcos, F; Uskov, S I; Snytnikov, P V; Hussainova, I

2017-12-20

Efficient capture and recycling of CO 2 enable not only prevention of global warming but also the supply of useful low-carbon fuels. The catalytic conversion of CO 2 into an organic compound is a promising recycling approach which opens new concepts and opportunities for catalytic and industrial development. Here we report about template-assisted wet-combustion synthesis of a one-dimensional nickel-based catalyst for carbon dioxide methanation and methane steam reforming. Because of a high temperature achieved in a short time during reaction and a large amount of evolved gases, the wet-combustion synthesis yields homogeneously precipitated nanoparticles of NiO with average particle size of 4 nm on alumina nanofibers covered with a NiAl 2 O 4 nanolayer. The as-synthesized core-shell structured fibers exhibit outstanding activity in steam reforming of methane and sufficient activity in carbon dioxide methanation with 100% selectivity toward methane formation. The as-synthesized catalyst shows stable operation under the reaction conditions for at least 50 h.

LABORATORY SCALE STEAM INJECTION TREATABILITY STUDIES

Science.gov (United States)

Laboratory scale steam injection treatability studies were first developed at The University of California-Berkeley. A comparable testing facility has been developed at USEPA's Robert S. Kerr Environmental Research Center. Experience has already shown that many volatile organic...

Conceptual design of a hydrogen production system by DME steam reforming and high-efficiency nuclear reactor technology

International Nuclear Information System (INIS)

Fukushima, Kimichika; Ogawa, Takashi

2003-01-01

Hydrogen is a potential alternative energy source and produced commercially by methane (natural gas) or LPG steam reforming, a process that requires high temperatures, which are produced by burning fossil fuels. However, since this process emits large amounts of CO 2 , replacement of the combustion heat source with a nuclear heat source for 773-1173 K processes has been proposed in order to eliminate these CO 2 emissions. This paper proposes a novel method of low-temperature nuclear hydrogen production by reforming dimethyl ether (DME) with steam produced by a low-temperature nuclear reactor at about 573 K. The authors identified conditions that provide high hydrogen production fraction at low pressure and temperatures of about 523-573 K. By setting this low-temperature hydrogen production process at about 573K upstream from a turbine, it was found theoretically that the total energy utilization efficiency is about 50% and very high. By setting a turbine upstream of the hydrogen production plant, an overall efficiency of is 75% for an FBR and 76% for a supercritical-water cooled power reactor (SCPR). (author)

Development of methane conversion improvement method by recycling of residual methane for steam reforming as a part of R and D of HTGR-hydrogen production system

International Nuclear Information System (INIS)

Inagaki, Yoshiyuki; Haga, Katsuhiro; Aita, Hideki; Sekita, Kenji; Hino, Ryutaro; Koiso, Hiroshi.

1998-01-01

The purpose of the present study is to improve methane conversion for an HTGR-steam reforming system by recycling of residual methane. The residual methane in a product gas after steam reforming was recycled with a gas separator of polyimide membrane. Gas separation characteristics of the separator were investigated experimentally and numerically, and an experimental study on recycling system was carried out. The results showed that the recycling system improves apparent methane conversion, ratio of methane conversion to methane supply from a cylinder, from 20 to 32% compared with those without recycling. (author)

Synthesis and Characterization of 1D Ceria Nanomaterials for CO Oxidation and Steam Reforming of Methanol

Directory of Open Access Journals (Sweden)

Sujan Chowdhury

2011-01-01

Full Text Available Novel one-dimensional (1D ceria nanostructure has been investigated as a promising and practical approach for the reforming of methanol reaction. Size and shape of the ceria nanomaterials are directly involved with the catalytic activities. Several general synthesis routes as including soft and hard template-assemble phenomenon for the preparation of 1D cerium oxide are discussed. This preparation phenomenon is consisting with low cost and ecofriendly. Nanometer-sized 1D structure provides a high-surface area that can interact with methanol and carbon-monoxide reaction. Overall, nanometer-sized structure provides desirable properties, such as easy recovery and regeneration. As a result, the use of 1D cerium has been suitable for catalytic application of reforming. In this paper, we describe the 1D cerium oxide syntheses route and then summarize their properties in the field of CO oxidation and steam reforming of methanol approach.

Modification of Catalysts for Steam Reforming of Fluid Hydrocarbons. Research of Gas-Dynamic Duct Cooling Using Planar and Framework Catalysts (CD-ROM)

National Research Council Canada - National Science Library

Kuranov, Alexander L

2005-01-01

.... One way of fuel conversion is the catalytic steam reforming of hydrocarbon. This reaction has a large heat capacity and gives maximum quantity of molecular hydrogen among known reactions of hydrocarbons...

A comparative economic assessment of hydrogen production from coke oven gas, water electrolysis and steam reforming of natural gas

International Nuclear Information System (INIS)

Nguyen, Y.V.; Ngo, Y.A.; Tinkler, M.J.; Cowan, N.

2003-01-01

This paper presents the comparative economics of producing hydrogen for the hydrogen economy by recovering it from waste gases from the steel industry, by water electrolysis and by conventional steam reforming of natural gas. Steel makers produce coke for their blast furnace operation by baking coal at high temperature in a reduced environment in their coke ovens. These ovens produce a coke oven gas from the volatiles in the coal. The gas, containing up to 60% hydrogen, is commonly used for its heating value with some of it being flared. The feasibility of recovering this hydrogen from the gas will be presented. A comparison of this opportunity with that of hydrogen from water electrolysis using low cost off-peak electricity from nuclear energy will be made. The impact of higher daily average electricity rate in Ontario will be discussed. The benefits of these opportunities compared with those from conventional steam reforming of natural gas will be highlighted. (author)

Renewable hydrogen production by catalytic steam reforming of peanut shells pyrolysis products

Energy Technology Data Exchange (ETDEWEB)

Evans, R.J.; Chornet, E.; Czernik, S.; Feik, C.; French, R.; Phillips, S. [National Renewable Energy Lab., Golden, CO (United States); Abedi, J.; Yeboah, Y.D. [Clark Atlanta Univ., Atlanta, GA (United States); Day, D.; Howard, J. [Scientific Carbons Inc., Blakely, GA (United States); McGee, D. [Enviro-Tech Enterprises Inc., Matthews, NC (United States); Realff, M.J. [Georgia Inst. of Technology, Atlanta, GA (United States)

2002-07-01

A project was initiated to determine the feasibility of producing hydrogen from agricultural wastes at a cost comparable to methane-reforming technologies. It is possible that hydrogen can be produced cost competitively with natural gas reforming by integrating hydrogen production with existing waste product utilization processes. This report presents initial results of an engineering demonstration project involving the development of a steam reforming process by a team of government, industrial and academic organizations working at the thermochemical facility at the National Renewable Energy Laboratory. The process is to be used on the gaseous byproducts from a process for making activated carbon from densified peanut shells. The reactor is interfaced with a 20 kg/hour fluidized-bed fast pyrolysis system and takes advantage of process chemical analysis and computer control and monitoring capacity. The reactor will be tested on the pyrolysis vapors produced in the activated carbon process. The final phase of the project will look at the production of hydrogen through the conversion of residual CO to H{sub 2} over a shift catalyst and separating hydrogen from CO{sub 2} using pressure swing adsorption. The purified oxygen will be mixed with natural gas and used for transportation purposes. The study demonstrates the potential impact of hydrogen and bioenergy on the economic development and diversification of rural areas. 11 refs., 2 tabs., 5 figs.

Hydrogen production by methanol steam reforming carried out in membrane reactor on Cu/Zn/Mg-based catalyst

NARCIS (Netherlands)

Basile, A.; Parmaliana, A.; Tosti, S.; Iulianelli, A.; Gallucci, F.; Espro, C.; Spooren, J.

2008-01-01

The methanol steam reforming (MSR) reaction was studied by using both a dense Pd-Ag membrane reactor (MR) and a fixed bed reactor (FBR). Both the FBR and the MR were packed with a new catalyst based on CuOAl2O3ZnOMgO, having an upper temperature limit of around 350 °C. A constant sweep gas flow rate

Small-scale reforming of diesel and jet fuels to make hydrogen and syngas for fuel cells: A review

International Nuclear Information System (INIS)

Xu, Xinhai; Li, Peiwen; Shen, Yuesong

2013-01-01

Highlights: • Issues of reforming of heavy hydrocarbon fuels are reviewed. • The advantages of autothermal reforming over other types of reforming are discussed. • The causes and solutions of the major problems for reforming reactors are studied. • Designs and startup strategies for autothermal reforming reactors are proposed. - Abstract: This paper reviews the technological features and challenges of autothermal reforming (ATR) of heavy hydrocarbon fuels for producing hydrogen and syngas onboard to supply fuels to fuel cells for auxiliary power units. A brief introduction at the beginning enumerates the advantages of using heavy hydrocarbon fuels onboard to provide hydrogen or syngas for fuel cells such as solid oxide fuel cells (SOFCs). A detailed review of the reforming and processing technologies of diesel and jet fuels is then presented. The advantages of ATR over steam reforming (SR) and partial oxidation reforming (POX) are summarized, and the ATR reaction is analyzed from a thermodynamic point of view. The causes and possible solutions to the major problems existing in ATR reactors, including hot spots, formation of coke, and inhomogeneous mixing of fuel, steam, and air, are reviewed and studied. Designs of ATR reactors are discussed, and three different reactors, one with a fixed bed, one with monoliths, and one with microchannels are investigated. Novel ideas for design and startup strategies for ATR reactors are proposed at the end of the review

Hydrogen-Rich Gas Production by Sorption Enhanced Steam Reforming of Woodgas Containing TAR over a Commercial Ni Catalyst and Calcined Dolomite as CO2 Sorbent

Directory of Open Access Journals (Sweden)

Vincenzo Naso

2013-07-01

Full Text Available The aim of this work was the evaluation of the catalytic steam reforming of a gaseous fuel obtained by steam biomass gasification to convert topping atmosphere residue (TAR and CH4 and to produce pure H2 by means of a CO2 sorbent. This experimental work deals with the demonstration of the practical feasibility of such concepts, using a real woodgas obtained from fluidized bed steam gasification of hazelnut shells. This study evaluates the use of a commercial Ni catalyst and calcined dolomite (CaO/MgO. The bed material simultaneously acts as reforming catalyst and CO2 sorbent. The experimental investigations have been carried out in a fixed bed micro-reactor rig using a slipstream from the gasifier to evaluate gas cleaning and upgrading options. The reforming/sorption tests were carried out at 650 °C while regeneration of the sorbent was carried out at 850 °C in a nitrogen environment. Both combinations of catalyst and sorbent are very effective in TAR and CH4 removal, with conversions near 100%, while the simultaneous CO2 sorption effectively enhances the water gas shift reaction producing a gas with a hydrogen volume fraction of over 90%. Multicycle tests of reforming/CO2 capture and regeneration were performed to verify the stability of the catalysts and sorbents to remove TAR and capture CO2 during the duty cycle.

MECHANISTIC KINETIC MODELS FOR STEAM REFORMING OF CONCENTRATED CRUDE ETHANOL ON NI/AL2O3 CATALYST

Directory of Open Access Journals (Sweden)

O. A. OLAFADEHAN

2015-05-01

Full Text Available Mechanistic kinetic models were postulated for the catalytic steam reforming of concentrated crude ethanol on a Ni-based commercial catalyst at atmosphere pressure in the temperature range of 673-863 K, and at different catalyst weight to the crude ethanol molar flow rate ratio (in the range 0.9645-9.6451 kg catalyst h/kg mole crude ethanol in a stainless steel packed bed tubular microreactor. The models were based on Langmuir-Hinshelwood-Hougen-Watson (LHHW and Eley-Rideal (ER mechanisms. The optimization routine of Nelder-Mead simplex algorithm was used to estimate the inherent kinetic parameters in the proposed models. The selection of the best kinetic model amongst the rival kinetic models was based on physicochemical, statistical and thermodynamic scrutinies. The rate determining step for the steam reforming of concentrated crude ethanol on Ni/Al2O3 catalyst was found to be surface reaction between chemisorbed CH3O and O when hydrogen and oxygen were adsorbed as monomolecular species on the catalyst surface. Excellent agreement was obtained between the experimental rate of reaction and conversion of crude ethanol, and the simulated results, with ADD% being ±0.46.

Scale Thickness Measurement of Steam Generator Tubing Using Eddy Current Signal of Bobbin Coil

International Nuclear Information System (INIS)

Kim, Chang Soo; Um, Ki Soo; Kim, Jae Dong

2012-01-01

Steam generator is one of the major components of nuclear power plant and steam generator tubes are the pressure boundary between primary and secondary side, which makes them critical for nuclear safety. As the operating time of nuclear power plant increases, not only damage mechanisms but also scaled deposits on steam generator tubes are known to be problematic causing tube support flow hole blockage and heat fouling. The ability to assess the extent and location of scaled deposits on tubes became essential for management and maintenance of steam generator and eddy current bobbin data can be utilized to measure thickness of scale on tubes. In this paper, tube reference standards with various thickness of scaled deposit has been set up to provide information about the overall deposit condition of steam generator tubes, providing essential tool for steam generator management and maintenance to predict and prevent future damages. Also, methodology to automatically measure scale thickness on tubes has been developed and applied to field data to estimate overall scale amount.

Demonstration of direct internal reforming for MCFC power plants

Energy Technology Data Exchange (ETDEWEB)

Aasberg-Petersen, K.; Christensen, P.S.; Winther, S.K. [HALDOR TOPSOE A/S, Lynby (Denmark)] [and others

1996-12-31

The conversion of methane into hydrogen for an MCFC by steam reforming is accomplished either externally or internally in the stack. In the case of external reforming the plant electrical efficiency is 5% abs. lower mainly because more parasitic power is required for air compression for stack cooling. Furthermore, heat produced in the stack must be transferred to the external reformer to drive the endothermic steam reforming reaction giving a more complex plant lay-out. A more suitable and cost effective approach is to use internal steam reforming of methane. Internal reforming may be accomplished either by Indirect Internal Reforming (DIR) and Direct Internal Reforming (DIR) in series or by DIR-only as illustrated. To avoid carbon formation in the anode compartment higher hydrocarbons in the feedstock are converted into hydrogen, methane and carbon oxides by reaction with steam in ail adiabatic prereformer upstream the fuel cell stack. This paper discusses key elements of the desire of both types of internal reforming and presents data from pilot plants with a combined total of more than 10,000 operating hours. The project is being carried out as part of the activities of the European MCFC Consortium ARGE.

Design and fabrication of a glovebox for the Plasma Hearth Process radioactive bench-scale system

International Nuclear Information System (INIS)

Wahlquist, D.R.

1996-01-01

This paper presents some of the design considerations and fabrication techniques for building a glovebox for the Plasma Hearth Process (PHP) radioactive bench-scale system. The PHP radioactive bench-scale system uses a plasma torch to process a variety of radioactive materials into a final vitrified waste form. The processed waste will contain plutonium and trace amounts of other radioactive materials. The glovebox used in this system is located directly below the plasma chamber and is called the Hearth Handling Enclosure (HHE). The HHE is designed to maintain a confinement boundary between the processed waste and the operator. Operations that take place inside the HHE include raising and lowering the hearth using a hydraulic lift table, transporting the hearth within the HHE using an overhead monorail and hoist system, sampling and disassembly of the processed waste and hearth, weighing the hearth, rebuilding a hearth, and sampling HEPA filters. The PHP radioactive bench-scale system is located at the TREAT facility at Argonne National Laboratory-West in Idaho Falls, Idaho

Embedded Sensors and Controls to Improve Component Performance and Reliability -- Bench-scale Testbed Design Report

Energy Technology Data Exchange (ETDEWEB)

Melin, Alexander M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Kisner, Roger A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Drira, Anis [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Reed, Frederick K. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2015-09-01

Embedded instrumentation and control systems that can operate in extreme environments are challenging due to restrictions on sensors and materials. As a part of the Department of Energy's Nuclear Energy Enabling Technology cross-cutting technology development programs Advanced Sensors and Instrumentation topic, this report details the design of a bench-scale embedded instrumentation and control testbed. The design goal of the bench-scale testbed is to build a re-configurable system that can rapidly deploy and test advanced control algorithms in a hardware in the loop setup. The bench-scale testbed will be designed as a fluid pump analog that uses active magnetic bearings to support the shaft. The testbed represents an application that would improve the efficiency and performance of high temperature (700 C) pumps for liquid salt reactors that operate in an extreme environment and provide many engineering challenges that can be overcome with embedded instrumentation and control. This report will give details of the mechanical design, electromagnetic design, geometry optimization, power electronics design, and initial control system design.

Comparative thermoeconomic analysis of hydrogen production by water electrolysis and by ethanol steam reforming

Energy Technology Data Exchange (ETDEWEB)

Riveros-Godoy, Gustavo; Chavez-Rodriguez, Mauro; Cavaliero, Carla [Universidade Estadual de Campinas (UNICAMP), Campinas, SP (Brazil). Mechanical Engineering School], Email: garg@fem.unicamp.br

2010-07-01

Hydrogen is the focus of this work that evaluates in comparative form through thermo economic analysis two hydrogen production processes: water electrolysis and ethanol steam reforming. Even though technical-economical barriers still exist for the development of an economy based on hydrogen, these difficulties are opportunities for the appearance of new business of goods and services, diversification of the energy mix, focus of research activities, development and support to provide sustainability to the new economy. Exergy and rational efficiency concept are used to make a comparison between both processes. (author)

Effects of electric current upon catalytic steam reforming of biomass gasification tar model compounds to syngas

International Nuclear Information System (INIS)

Tao, Jun; Lu, Qiang; Dong, Changqing; Du, Xiaoze; Dahlquist, Erik

2015-01-01

Highlights: • ECR technique was proposed to convert biomass gasification tar model compounds. • Electric current enhanced the reforming efficiency remarkably. • The highest toluene conversion reached 99.9%. • Ni–CeO 2 /γ-Al 2 O 3 exhibited good stability during the ECR performance. - Abstract: Electrochemical catalytic reforming (ECR) technique, known as electric current enhanced catalytic reforming technique, was proposed to convert the biomass gasification tar into syngas. In this study, Ni–CeO 2 /γ-Al 2 O 3 catalyst was prepared, and toluene was employed as the major feedstock for ECR experiments using a fixed-bed lab-scale setup where thermal electrons could be generated and provided to the catalyst. Several factors, including the electric current intensity, reaction temperature and steam/carbon (S/C) ratio, were investigated to reveal their effects on the conversion of toluene as well as the composition of the gas products. Moreover, toluene, two other tar model compounds (benzene and 1-methylnaphthalene) and real tar (tar-containing wastewater) were subjected to the long period catalytic stability tests. All the used catalysts were analyzed to determine their carbon contents. The results indicated that the presence of electric current enhanced the catalytic performance remarkably. The toluene conversion reached 99.9% under the electric current of 4 A, catalytic temperature of 800 °C and S/C ratio of 3. Stable conversion performances of benzene, 1-methylnaphthalene and tar-containing wastewater were also observed in the ECR process. H 2 and CO were the major gas products, while CO 2 and CH 4 were the minor ones. Due to the promising capability, the ECR technique deserves further investigation and application for efficient tar conversion

Kinetics study of ethanol steam reforming on Pt/CeO{sub 2} based catalysts

Energy Technology Data Exchange (ETDEWEB)

Qi, A. [Queen' s-RMC Fuel Cell Research Centre, Kingston, ON (Canada). Dept. of Chemistry and Chemical Engineering; Thurgood, C.; Amphlett, J. [Royal Military College of Canada, Kingston, ON (Canada). Dept. of Chemistry and Chemical Engineering; Peppley, B. [Queens Univ., Kingston, ON (Canada). Dept. of Chemical Engineering

2009-07-01

Interest in fuel cell systems operating on fuels derived from renewable energy sources is increasing because they have the potential to produce electricity with high efficiency and minimal emissions of carbon dioxide and other pollutants. Bioethanol is currently produced by the fermentation of non-edible biomass, through conventional means and also through advances in enzyme technology. The authors previously reported on the steam reforming of bioethanol with a stable ceria supported precious metal catalyst, developed in-house. The catalyst had good thermal stability and resisted carbon formation. This paper reported on a more recent kinetic study in which the influence of operating conditions were quantified. The operating conditions included temperature, steam/carbon ratios, and gas hourly velocities. The results of standard catalyst characterization techniques such as BET, TGA, SEM and TPR were also provided. The data was used to drive an empirical rate expression. The study also investigated a potential rate mechanism.

Bench-Scale Development of a Non-Aqueous Solvent (NAS) CO2 Capture Process for Coal-Fired Power Plants

Energy Technology Data Exchange (ETDEWEB)

Lail, Marty

2017-09-12

The project aimed to advance RTI’s non-aqueous amine solvent technology by improving the solvent to reduce volatility, demonstrating long-term continuous operation at lab- (0.5 liters solvent) and bench-scale (~120 liters solvent), showing low reboiler heat duty measured during bench-scale testing, evaluating degradation products, building a rate-based process model, and evaluating the techno-economic performance of the process. The project team (RTI, SINTEF, Linde Engineering) and the technology performed well in each area of advancement. The modifications incorporated throughout the project enabled the attainment of target absorber and regenerator conditions for the process. Reboiler duties below 2,000 kJt/kg CO2 were observed in a bench-scale test unit operated at RTI.

Bench-Scale Demonstration of Hot-Gas Desulfurization Technology

International Nuclear Information System (INIS)

Portzer, Jeffrey W.; Gangwal, Santosh K.

1997-01-01

Prior to the current project, development of the DSRP was done in a laboratory setting, using synthetic gas mixtures to simulate the regeneration off-gas and coal gas feeds. The objective of the current work is to further the development of zinc titanate fluidized-bed desulfurization (ZTFBD) and the DSRP for hot-gas cleanup by testing with actual coal gas. The objectives of this project are to: (1) Develop and test an integrated, skid-mounted, bench-scale ZTFBD/DSRP reactor system with a slipstream of actual coal gas; (2) Test the bench-scale DSRP over an extended period with a slipstream of actual coal gas to quantify the degradation in performance, if any, caused by the trace contaminants present in coal gas (including heavy metals, chlorides, fluorides, and ammonia); (3) Expose the DSRP catalyst to actual coal gas for extended periods and then test its activity in a laboratory reactor to quantify the degradation in performance, if any, caused by static exposure to the trace contaminants in coal gas; (4) Design and fabricate a six-fold larger-scale DSRP reactor system for future slipstream testing; (5) Further develop the fluidized-bed DSRP to handle high concentrations (up to 14 percent) of SO 2 that are likely to be encountered when pure air is used for regeneration of desulfurization sorbents; and (6) Conduct extended field testing of the 6X DSRP reactor with actual coal gas and high concentrations of SO 2 . The accomplishment of the first three objectives--testing the DSRP with actual coal gas, integration with hot-gas desulfurization, and catalyst exposure testing--was described previously (Portzer and Gangwal, 1994, 1995; Portzer et al., 1996). This paper summarizes the results of previous work and describes the current activities and plans to accomplish the remaining objectives

FLUIDIZED BED STEAM REFORMER (FBSR) PRODUCT: MONOLITH FORMATION AND CHARACTERIZATION

International Nuclear Information System (INIS)

Jantzen, C

2006-01-01

) durability must not be compromised--binding agent should not react with the NAS product and binding agent should not create an unfavorable pH environment that may cause accelerated leaching. It is the goal of the present study to survey cementitious waste forms based on Ordinary Portland Cement (OPC), Ceramicrete, and hydroceramic binders by correlating waste loading, density and compressive strength and then determine if these binders affect the product performance in terms of the PCT response. This will be done by making a one-to-one comparison of the PCT response measured on granular NAS mineral product (mixed bed and fines products) with the PCT response of the monolithed NAS product in the different binders. Future studies may include, refining the above binders, and examining other binders. It is likely that binders formed from kaolin would be most compatible with the chemistry of the THOR(reg s ign) mineral waste form which is made by steam reforming of kaolin and sodium rich wastes. The economics of production on a large scale have yet to be investigated for any of the binders tested

Hydrogen production through sorption-enhanced steam methane reforming and membrane technology: A review

International Nuclear Information System (INIS)

Barelli, L.; Bidini, G.; Gallorini, F.; Servili, S.

2008-01-01

With the rapid development of industry, more and more waste gases are emitted into the atmosphere. In terms of total air emissions, CO 2 is emitted in the greatest amount, accounting for 99 wt% of the total air emissions, therefore contributing to global warming, the so-called 'Greenhouse Effect'. The recovery and disposal of CO 2 from flue gas is currently the object of great international interest. Most of the CO 2 comes from the combustion of fossil fuels in power generation, industrial boilers, residential and commercial heating, and transportation sectors. Consequently, in the last years' interest in hydrogen as an energy carrier has significantly increased both for vehicle fuelling and stationary energy production from fuel cells. The benefits of a hydrogen energy policy are the reduction of the greenhouse effect, principally due to the centralization of the emission sources. Moreover, an improvement to the environmental benefits can be achieved if hydrogen is produced from renewable sources, as biomass. The present paper provides an overview of the steam methane reforming (SMR) process and methodologies for performances improvement such as hydrogen removal, by selective permeation through a membrane or simultaneous reaction of the targeted molecule with a chemical acceptor, and equilibrium shift by the addition of a CO 2 acceptor to the reactor. In particular, attention was focused on the sorption-enhanced steam methane reforming (SE-SMR) process in which sorbents are added in order to enhance the reactions and realize in situ CO 2 separation. The major operating parameters of SE-SMR are described by the authors in order to project and then realize the innovative carbonation reactor developed in previous studies

Eight attention points when evaluating large-scale public sector reforms

DEFF Research Database (Denmark)

Hansen, Morten Balle; Breidahl, Karen Nielsen; Furubo, Jan-Eric

2017-01-01

This chapter analyses the challenges related to evaluations of large-scale public sector reforms. It is based on a meta-evaluation of the evaluation of the reform of the Norwegian Labour Market and Welfare Administration (the NAV-reform) in Norway, which entailed both a significant reorganization...... sector reforms. Based on the analysis, eight crucial points of attention when evaluating large-scale public sector reforms are elaborated. We discuss their reasons and argue that other countries will face the same challenges and thus can learn from the experiences of Norway....

Numerical analysis of hydrogen production via methane steam reforming in porous media solar thermochemical reactor using concentrated solar irradiation as heat source

International Nuclear Information System (INIS)

Wang, Fuqiang; Tan, Jianyu; Shuai, Yong; Gong, Liang; Tan, Heping

2014-01-01

Highlights: • H 2 production by hybrid solar energy and methane steam reforming is analyzed. • MCRT and FVM coupling method is used for chemical reaction in solar porous reactor. • LTNE model is used to study the solid phase and fluid phase thermal performance. • Modified P1 approximation programmed by UDFs is used for irradiative heat transfer. - Abstract: The calorific value of syngas can be greatly upgraded during the methane steam reforming process by using concentrated solar energy as heat source. In this study, the Monte Carlo Ray Tracing (MCRT) and Finite Volume Method (FVM) coupling method is developed to investigate the hydrogen production performance via methane steam reforming in porous media solar thermochemical reactor which includes the mass, momentum, energy and irradiative transfer equations as well as chemical reaction kinetics. The local thermal non-equilibrium (LTNE) model is used to provide more temperature information. The modified P1 approximation is adopted for solving the irradiative heat transfer equation. The MCRT method is used to calculate the sunlight concentration and transmission problems. The fluid phase energy equation and transport equations are solved by Fluent software. The solid phase energy equation, irradiative transfer equation and chemical reaction kinetics are programmed by user defined functions (UDFs). The numerical results indicate that concentrated solar irradiation on the fluid entrance surface of solar chemical reactor is highly uneven, and temperature distribution has significant influence on hydrogen production

Hydrogen Production via Steam Reforming of Ethyl Alcohol over Palladium/Indium Oxide Catalyst

Directory of Open Access Journals (Sweden)

Tetsuo Umegaki

2009-01-01

Full Text Available We report the synergetic effect between palladium and indium oxide on hydrogen production in the steam reforming reaction of ethyl alcohol. The palladium/indium oxide catalyst shows higher hydrogen production rate than indium oxide and palladium. Palladium/indium oxide affords ketonization of ethyl alcohol with negligible by-product carbon monoxide, while indium oxide mainly affords dehydration of ethyl alcohol, and palladium affords decomposition of ethyl alcohol with large amount of by-product carbon monoxide. The catalytic feature of palladium/indium oxide can be ascribed to the formation of palladium-indium intermetallic component during the reaction as confirmed by X-ray diffraction and X-ray photoelectron spectroscopic measurements.

DURABILITY TESTING OF FLUIDIZED BED STEAM REFORMER (FBSR) WASTE FORMS

International Nuclear Information System (INIS)

Jantzen, C

2006-01-01

Fluidized Bed Steam Reforming (FBSR) is being considered as a potential technology for the immobilization of a wide variety of high sodium aqueous radioactive wastes. The addition of clay and a catalyst as co-reactants converts high sodium aqueous low activity wastes (LAW) such as those existing at the Hanford and Idaho DOE sites to a granular ''mineralized'' waste form that may be made into a monolith form if necessary. Simulant Hanford and Idaho high sodium wastes were processed in a pilot scale FBSR at Science Applications International Corporation (SAIC) Science and Technology Applications Research (STAR) facility in Idaho Falls, ID. Granular mineral waste forms were made from (1) a basic Hanford Envelope A low-activity waste (LAW) simulant and (2) an acidic INL simulant commonly referred to as sodium-bearing waste (SBW). The FBSR waste forms were characterized and the durability tested via ASTM C1285 (Product Consistency Test), the Environmental Protection Agency (EPA) Toxic Characteristic Leaching Procedure (TCLP), and the Single Pass Flow Through (SPFT) test. The durability of the FBSR waste form products was tested in order to compare the measured durability to previous FBSR waste form testing on Hanford Envelope C waste forms that were made by THOR Treatment Technologies (TTT) and to compare the FBSR durability to vitreous LAW waste forms, specifically the Hanford low activity waste (LAW) glass known as the Low-activity Reference Material (LRM). The durability of the FBSR waste form is comparable to that of the LRM glass for the test responses studied

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

thermal analysis of a small scale solid waste-fired steam boiler

African Journals Online (AJOL)

user

Thermal analysis of a small scale solid waste-fired steam generator is presented in this paper. The analysis was based on the chosen design specifications which are operating steam ... include: wind, bio-energy, geothermal, solar thermal,.

Effectiveness factors for a commercial steam reforming (Ni) catalyst and for a calcined dolomite used downstream biomass gasifiers

Energy Technology Data Exchange (ETDEWEB)

Corella, J; Narvaez, I; Orio, A [Madrid Univ. (Spain). Dept. of Chem. Eng.

1997-12-31

A commercial steam reforming catalyst from BASF, the G1-25 S one, and a calcined dolomite, Norte-1, from Cantabria-Spain, have been used, once crushed and sieved to different particle fractions between 1.0 and 4.0 mm. The materials have been tested downstream small pilot biomass gasifiers, bubbling fluidized bed type, gasifying with air and with steam. The Thiele modulus and the effectiveness factor have been calculated at temperatures of 750-850 deg C. It is experimentally shown that diffusion control plays an important part when particle size is larger than ca. 0.5 mm. This has to be taken into account when comparing the quality of the solids for tar elimination. (author) (5 refs.)

Effectiveness factors for a commercial steam reforming (Ni) catalyst and for a calcined dolomite used downstream biomass gasifiers

Energy Technology Data Exchange (ETDEWEB)

Corella, J.; Narvaez, I.; Orio, A. [Madrid Univ. (Spain). Dept. of Chem. Eng.

1996-12-31

A commercial steam reforming catalyst from BASF, the G1-25 S one, and a calcined dolomite, Norte-1, from Cantabria-Spain, have been used, once crushed and sieved to different particle fractions between 1.0 and 4.0 mm. The materials have been tested downstream small pilot biomass gasifiers, bubbling fluidized bed type, gasifying with air and with steam. The Thiele modulus and the effectiveness factor have been calculated at temperatures of 750-850 deg C. It is experimentally shown that diffusion control plays an important part when particle size is larger than ca. 0.5 mm. This has to be taken into account when comparing the quality of the solids for tar elimination. (author) (5 refs.)

Economic analysis of hydrogen production through a bio-ethanol steam reforming process: Sensitivity analyses and cost estimations

International Nuclear Information System (INIS)

Song, Hua; Ozkan, Umit S.

2010-01-01

In this study, the hydrogen selling price from ethanol steam reforming has been estimated for two different production scenarios in the United States, i.e. central production (150,000 kg H 2 /day) and distributed (forecourt) production (1500 kg H 2 /day), based on a process flowchart generated by Aspen Plus registered including downstream purification steps and economic analysis model template published by the U.S Department of Energy (DOE). The effect of several processing parameters as well as catalyst properties on the hydrogen selling price has been evaluated. 2.69/kg is estimated as the selling price for a central production process of 150,000 kg H 2 /day and 4.27/kg for a distributed hydrogen production process at a scale of 1500 kg H 2 /day. Among the parameters investigated through sensitivity analyses, ethanol feedstock cost, catalyst cost, and catalytic performance are found to play a significant role on determining the final hydrogen selling price. (author)

Structured reactors as alternative to pellets catalyst for propane oxidative steam reforming

Energy Technology Data Exchange (ETDEWEB)

Vita, A.; Pino, L.; Cipiti, F.; Lagana, M.; Recupero, V. [CNR - Institute for Advanced Energy Technologies ' ' Nicola Giordano' ' , Via Salita S. Lucia sopra Contesse n. 5, 98126 Messina (Italy)

2010-09-15

The performance of a Pt/CeO{sub 2} catalyst as packed bed, coated on monolith and as self-structured bed has been evaluated during C{sub 3}H{sub 8} oxidative steam reforming. Structured bed, prepared by a new aqueous tape casting method, combining high total porosity (80%) with a self-supported channel structure, offers a better and more efficient control of heat and mass transfer along the catalytic bed, showing, especially at high gas hourly space velocity (30 x 10{sup 4} h{sup -1}), better performance in terms of fuel conversion, hydrogen production and low by-products formation coupled with an economy of the catalyst of about to 43% with respect to the traditional packed bed system. (author)

On direct internal methane steam reforming kinetics in operating solid oxide fuel cells with nickel-ceria anodes

Science.gov (United States)

Thallam Thattai, A.; van Biert, L.; Aravind, P. V.

2017-12-01

Major operating challenges remain to safely operate methane fuelled solid oxide fuel cells due to undesirable temperature gradients across the porous anode and carbon deposition. This article presents an experimental study on methane steam reforming (MSR) global kinetics for single operating SOFCs with Ni-GDC (gadolinium doped ceria) anodes for low steam to carbon (S/C) ratios and moderate current densities. The study points out the hitherto insufficient research on MSR global and intrinsic kinetics for operating SOFCs with complete Ni-ceria anodes. Further, it emphasizes the need to develop readily applicable global kinetic models as a subsequent step from previously reported state-of-art and complex intrinsic models. Two rate expressions of the Power law (PL) and Langmuir-Hinshelwood (LH) type have been compared and based on the analysis, limitations of using previously proposed rate expressions for Ni catalytic beds to study MSR kinetics for complete cermet anodes have been identified. Firstly, it has been shown that methane reforming on metallic (Ni) current collectors may not be always negligible, contrary to literature reports. Both PL and LH kinetic models predict significantly different local MSR reaction rate and species partial pressure distributions along the normalized reactor length, indicating a strong need for further experimental verifications.

Investigation of methane steam reforming in planar porous support of solid oxide fuel cell

International Nuclear Information System (INIS)

Yang Yongping; Du Xiaoze; Yang Lijun; Huang Yuan; Xian Haizhen

2009-01-01

Adopting the porous support in integrated-planar solid oxide fuel cell (IP-SOFC) can reduce the operating temperature by reducing thickness of electrolyte layer, and also, provide internal reforming environment for hydrogen-rich fuel gas. The distributions of reactant and product components, and temperature of methane steam reforming for IP-SOFC were investigated by the developed physical and mathematical model with thermodynamic analysis, in which eleven possible reaction mechanisms were considered by the source terms and Arrhenius relationship. Numerical simulation of the model revealed that the progress of reforming reaction and the distribution of the product, H 2 , were influenced by the operating conditions, included that of temperature, ratio of H 2 O and CH 4 , as well as by the porosity of the supporting material. The simulating results indicate that the methane conversion rate can reach its maximum value under the operating temperature of 800 deg. C and porosity of ε = 0.4, which rather approximate to the practical operating conditions of IP-SOFC. In addition, characteristics of carbon deposition on surface of catalyst were discussed under various operating conditions and configuration parameters of the porous support. The present works provided some theoretical explanations to the numerous experimental observations and engineered practices

Steam reforming of bio-ethanol over Ni on Ce-ZrO2 support: Influence of redox properties on the catalyst reactivity

Directory of Open Access Journals (Sweden)

Sumittra Charojrochkul

2006-11-01

Full Text Available The steam reforming of ethanol over Ni on Ce-ZrO2 support, (Ni/ Ce-ZrO2 were studied. The catalyst provides significantly higher reforming reactivity and excellent resistance toward carbon deposition compared to Ni/Al2O3 under the same conditions. At the temperature above 800ºC, the main products from the reforming processes over Ni/Ce-ZrO2 were H2, CO, and CO2 with small amount of CH4 depending on the inlet ethanol/steam and oxygen/ethanol ratios, whereas high hydrocarbon compounds i.e., C2H4 and C2H6 were also observed from the reforming of ethanol over Ni/Al2O3 in the range of conditions studied (700- 1000ºC.These excellent ethanol reforming performances of Ni/Ce-ZrO2 in terms of stability, reactivity and product selectivities are due to the high redox property of Ce-ZrO2. During the ethanol reforming process, in addition to the reactions on Ni surface, the gas-solid reactions between the gaseous components presented in the system (C2H5OH, C2H6, C2H4, CH4, CO2, CO, H2O, and H2 and the lattice oxygen (Ox on Ce-ZrO2 surface also take place. Among these redox reactions, the reactions of adsorbed surface hydrocarbons with the lattice oxygen (Ox (CnHm + Ox → nCO + m/2(H2 + Ox-n can eliminate the formation of high hydrocarbons (C2H6 and C2H4, which easily decompose and form carbon species on Ni surface (CnHm→ nC + m/2H2.

Hydrogen production by biomass steam gasification in fluidized bed reactor with Co catalyst

International Nuclear Information System (INIS)

Kazuhiko Tasaka; Atsushi Tsutsumi; Takeshi Furusawa

2006-01-01

The catalytic performances of Co/MgO catalysts were investigated in steam gasification of cellulose and steam reforming of tar derived from cellulose gasification. For steam reforming of cellulose tar in a secondary fixed bed reactor, 12 wt.% Co/MgO catalyst attained more than 80% of tar reduction. The amount of produced H 2 and CO 2 increased with the presence of catalyst, and kept same level during 2 hr at 873 K. It is indicated that steam reforming of cellulose tar proceeds sufficiently over Co/MgO catalyst. For steam gasification of cellulose in a fluidized bed reactor, it was found that tar reduction increases with Co loading amount and 36 wt.% Co/MgO catalyst showed 84% of tar reduction. The amounts of produced gas kept for 2 hr indicating that 36 wt.% Co/MgO catalyst is stable during the reaction. It was concluded that these Co catalysts are promising systems for the steam gasification of cellulose and steam reforming of cellulose tar. (authors)

Investigation of Fuel Chemistry and Bed Performance in a Fluidized Bed Black Liquor Steam Reformer

Energy Technology Data Exchange (ETDEWEB)

Kevin Whitty

2007-06-30

University of Utah's project entitled 'Investigation of Fuel Chemistry and Bed Performance in a Fluidized Bed Black Liquor Steam Reformer' (DOE Cooperative Agreement DE-FC26-02NT41490) was developed in response to a solicitation released by the U.S. Department of Energy in December 2001, requesting proposals for projects targeted towards black liquor/biomass gasification technology support research and development. Specifically, the solicitation was seeking projects that would provide technical support for Department of Energy supported black liquor and biomass gasification demonstration projects under development at the time.

Catalytic multi-stage liquefaction of coal at HTI: Bench-scale studies in coal/waste plastics coprocessing

Energy Technology Data Exchange (ETDEWEB)

Pradhan, V.R.; Lee, L.K.; Stalzer, R.H. [Hydrocarbon Technologies, Inc., Lawrenceville, NJ (United States)] [and others

1995-12-31

The development of Catalytic Multi-Stage Liquefaction (CMSL) at HTI has focused on both bituminous and sub-bituminous coals using laboratory, bench and PDU scale operations. The crude oil equivalent cost of liquid fuels from coal has been curtailed to about $30 per barrel, thus achieving over 30% reduction in the price that was evaluated for the liquefaction technologies demonstrated in the late seventies and early eighties. Contrary to the common belief, the new generation of catalytic multistage coal liquefaction process is environmentally very benign and can produce clean, premium distillates with a very low (<10ppm) heteroatoms content. The HTI Staff has been involved over the years in process development and has made significant improvements in the CMSL processing of coals. A 24 month program (extended to September 30, 1995) to study novel concepts, using a continuous bench scale Catalytic Multi-Stage unit (30kg coal/day), has been initiated since December, 1992. This program consists of ten bench-scale operations supported by Laboratory Studies, Modelling, Process Simulation and Economic Assessments. The Catalytic Multi-Stage Liquefaction is a continuation of the second generation yields using a low/high temperature approach. This paper covers work performed between October 1994- August 1995, especially results obtained from the microautoclave support activities and the bench-scale operations for runs CMSL-08 and CMSL-09, during which, coal and the plastic components for municipal solid wastes (MSW) such as high density polyethylene (HDPE)m, polypropylene (PP), polystyrene (PS), and polythylene terphthlate (PET) were coprocessed.

Advanced Catalysis Technologies: Lanthanum Cerium Manganese Hexaaluminate Combustion Catalysts for Flat Plate Reactor for Compact Steam Reformers

Science.gov (United States)

2008-12-01

packed-bed steam reformer reactor using an open-flame or radiant burner as the heat source, the rate of heat transfer is limited by wall film and bed...resistances. Heat transfer can be effectively improved by replacing the burner /packed-bed system with parallel channels containing metal foam...combustion reactor was tested using the hexaaluminate catalyst in pellets and supported on FeCrAlloy metal foam. Both tests burned propane and JP-8

Optimization of a Pd-based membrane reactor for hydrogen production from methane steam reforming

Energy Technology Data Exchange (ETDEWEB)

Assis, A.J.; Hori, C.E.; Silva, L.C.; Murata, V.V. [Universidade Federal de Uberlandia (UFU), MG (Brazil). School of Chemical Engineering]. E-mail: adilsonjassis@gmail.com

2008-07-01

In this work, it is proposed a phenomenological model in steady state to describe the performance of a membrane reactor for hydrogen production through methane steam reform as well as it is performed an optimization of operating conditions. The model is composed by a set of ordinary differential equations from mass, energy and momentum balances and constitutive relations. They were used two different intrinsic kinetic expressions from literature. The results predicted by the model were validated using experimental data. They were investigated the effect of five important process parameters, inlet reactor pressure (PR0), methane feed flow rate (FCH40), sweep gas flow rate (FI), external reactor temperature (TW) and steam to methane feed flow ratio (M), both on methane conversion (XCH{sub 4} ) and hydrogen recovery (YH{sub 2}). The best operating conditions were obtained through simple parametric optimization and by a method based on gradient, which uses the computer code DIRCOL in FORTRAN. It is shown that high methane conversion (96%) as well as hydrogen recovery (91%) can be obtained, using the optimized conditions. (author)

Hydrogen production by steam reforming of liquefied natural gas (LNG) over nickel catalysts supported on cationic surfactant-templated mesoporous aluminas

Science.gov (United States)

Seo, Jeong Gil; Youn, Min Hye; Park, Sunyoung; Jung, Ji Chul; Kim, Pil; Chung, Jin Suk; Song, In Kyu

Two types of mesoporous γ-aluminas (denoted as A-A and A-S) are prepared by a hydrothermal method under different basic conditions using cationic surfactant (cetyltrimethylammonium bromide, CTAB) as a templating agent. A-A and A-S are synthesized in a medium of ammonia solution and sodium hydroxide solution, respectively. Ni/γ-Al 2O 3 catalysts (Ni/A-A and Ni/A-S) are then prepared by an impregnation method, and are applied to hydrogen production by steam reforming of liquefied natural gas (LNG). The effect of a mesoporous γ-Al 2O 3 support on the catalytic performance of Ni/γ-Al 2O 3 is investigated. The identity of basic solution strongly affects the physical properties of the A-A and A-S supports. The high surface-area of the mesoporous γ-aluminas and the strong metal-support interaction of supported catalysts greatly enhance the dispersion of nickel species on the catalyst surface. The well-developed mesopores of the Ni/A-A and Ni/A-S catalysts prohibit the polymerization of carbon species on the catalyst surface during the reaction. In the steam reforming of LNG, both Ni/A-A and Ni/A-S catalysts give better catalytic performance than the nickel catalyst supported on commercial γ-Al 2O 3 (Ni/A-C). In addition, the Ni/A-A catalyst is superior to the Ni/A-S catalyst. The relatively strong metal-support interaction of Ni/A-A catalyst effectively suppresses the sintering of metallic nickel and the carbon deposition in the steam reforming of LNG. The large pores of the Ni/A-A catalyst also play an important role in enhancing internal mass transfer during the reaction.

Methanol steam reforming over Cu/CeO2 catalysts: influence of zinc addition

Directory of Open Access Journals (Sweden)

Franco Tonelli

2011-01-01

Full Text Available Methanol steam reforming reaction was studied over Cu(5 wt.%/CeO2 with and without the presence of Zn. The Zn addition decreased the Cu+2 reducibility and increased the oxygen mobility of ceria. The main products were CO2 and H2 with small amount of CO. Selectivity to CO decreased with the Zn addition and it was lower at lower reaction temperatures and lower space velocities. At 230 ºC and W/F MeOH = 648 g min mol-1 selectivities to H2 and to CO2 were 100% on Zn/Cu/Ce. The catalytic results indicated that CO was mainly a secondary product formed from reverse water gas shift reaction.

Hydrogen Production by Steam Reforming of Liquefied Natural Gas (LNG) Over Nickel-Phosphorus-Alumina Xerogel Catalyst Prepared by a Carbon-Templating Epoxide-Driven Sol-Gel Method.

Science.gov (United States)

Bang, Yongju; Park, Seungwon; Han, Seung Ju; Yoo, Jaekyeong; Choi, Jung Ho; Kang, Tae Hun; Lee, Jinwon; Song, In Kyu

2016-05-01

A nickel-phosphorus-alumina xerogel catalyst was prepared by a carbon-templating epoxide-driven sol-gel method (denoted as CNPA catalyst), and it was applied to the hydrogen production by steam reforming of liquefied natural gas (LNG). For comparison, a nickel-phosphorus-alumina xerogel catalyst was also prepared by a similar method in the absence of carbon template (denoted as NPA catalyst). The effect of carbon template addition on the physicochemical properties and catalytic activities of the catalysts in the steam reforming of LNG was investigated. Both CNPA and NPA catalysts showed excellent textural properties with well-developed mesoporous structure. However, CNPA catalyst retained a more reducible nickel aluminate phase than NPA catalyst. XRD analysis of the reduced CNPA and NPA catalysts revealed that nickel sintering on the CNPA catalyst was suppressed compared to that on the NPA catalyst. From H2-TPD and CH4-TPD measurements of the reduced CNPA and NPA catalysts, it was also revealed that CNPA catalyst with large amount of hydrogen uptake and strong hydrogen-binding sites showed larger amount of methane adsorption than NPA catalyst. In the hydrogen production by steam reforming of LNG, CNPA catalyst with large methane adsorption capacity showed a better catalytic activity than NPA catalyst.

High temperature ceramic-tubed reformer

Science.gov (United States)

Williams, Joseph J.; Rosenberg, Robert A.; McDonough, Lane J.

1990-03-01

The overall objective of the HiPHES project is to develop an advanced high-pressure heat exchanger for a convective steam/methane reformer. The HiPHES steam/methane reformer is a convective, shell and tube type, catalytic reactor. The use of ceramic tubes will allow reaction temperature higher than the current state-of-the-art outlet temperatures of about 1600 F using metal tubes. Higher reaction temperatures increase feedstock conversion to synthesis gas and reduce energy requirements compared to currently available radiant-box type reformers using metal tubes. Reforming of natural gas is the principal method used to produce synthesis gas (primarily hydrogen and carbon monoxide, H2 and CO) which is used to produce hydrogen (for refinery upgrading), methanol, as well as several other important materials. The HiPHES reformer development is an extension of Stone and Webster's efforts to develop a metal-tubed convective reformer integrated with a gas turbine cycle.

Thermal and chemical analysis of carbon dioxide reforming of methane using the out-of-pile test facility

International Nuclear Information System (INIS)

Huang Ziyong; Ohashi, Hirofumi; Inagaki, Yoshiyuki

2000-03-01

In the Japan Atomic Energy Research Institute, a hydrogen production system is being designed to produce hydrogen by means of steam reforming of natural gas (its main composition is methane(CH 4 )) using nuclear heat (10 MW, 1178 K) supplied by the High Temperature Engineering Test Reactor (HTTR). Prior to coupling of the steam reforming system with the HTTR, an out-of-pile demonstration test was planned to confirm safety, controllability and performance of the steam reforming system under simulated operational conditions of the prototype. The out-of-pile test facility simulates key components downstream to an intermediate heat exchanger of the HTTR hydrogen production system on a scale of 1 : 30 and has a hydrogen production capacity of 110 Nm 3 /h using an electric heater as a reactor substitute. The test facility is presently under construction. Reforming of natural gas with carbon dioxide CO 2 (CO 2 reforming) using the out-of-pile test facility is also being considered. In recent years, catalytic reforming of natural gas with CO 2 to synthesis gas (CO and H 2 ) has been proposed as one of the most promising technologies for utilization of those two greenhouse gases. Numerical analysis on heat and mass balance has practical significance in CO 2 reforming when the steam reforming process is adopted in the out-of-pile test. Numerical analysis of CO 2 reforming and reforming of natural gas with CO 2 and steam (CO 2 +H 2 O reforming) have been carried out using the mathematical model. Results such as the methane conversion rate, product gas composition, and the components temperature distribution considering the effects of helium gas temperature, reforming pressure, molar ratio of process gases and so on have been obtained in the numerical analysis. Heat and mass balance of the out-of-pile test facility considering chemical reactions are evaluated well. The methane conversation rates are about 0.36 and 0.35 which correspond to the equilibrium at 1085 and 1100 K for

Thermal and chemical analysis of carbon dioxide reforming of methane using the out-of-pile test facility

Energy Technology Data Exchange (ETDEWEB)

Huang Ziyong [Institute of Nuclear Energy Technology, Tsinghua University (China); Ohashi, Hirofumi; Inagaki, Yoshiyuki [Department of Advanced Nuclear Heat Technology, Oarai Research Establishment, Japan Atomic Energy Research Institute, Oarai, Ibaraki (Japan)

2000-03-01

In the Japan Atomic Energy Research Institute, a hydrogen production system is being designed to produce hydrogen by means of steam reforming of natural gas (its main composition is methane(CH{sub 4})) using nuclear heat (10 MW, 1178 K) supplied by the High Temperature Engineering Test Reactor (HTTR). Prior to coupling of the steam reforming system with the HTTR, an out-of-pile demonstration test was planned to confirm safety, controllability and performance of the steam reforming system under simulated operational conditions of the prototype. The out-of-pile test facility simulates key components downstream to an intermediate heat exchanger of the HTTR hydrogen production system on a scale of 1 : 30 and has a hydrogen production capacity of 110 Nm{sup 3}/h using an electric heater as a reactor substitute. The test facility is presently under construction. Reforming of natural gas with carbon dioxide CO{sub 2} (CO{sub 2} reforming) using the out-of-pile test facility is also being considered. In recent years, catalytic reforming of natural gas with CO{sub 2} to synthesis gas (CO and H{sub 2}) has been proposed as one of the most promising technologies for utilization of those two greenhouse gases. Numerical analysis on heat and mass balance has practical significance in CO{sub 2} reforming when the steam reforming process is adopted in the out-of-pile test. Numerical analysis of CO{sub 2} reforming and reforming of natural gas with CO{sub 2} and steam (CO{sub 2}+H{sub 2}O reforming) have been carried out using the mathematical model. Results such as the methane conversion rate, product gas composition, and the components temperature distribution considering the effects of helium gas temperature, reforming pressure, molar ratio of process gases and so on have been obtained in the numerical analysis. Heat and mass balance of the out-of-pile test facility considering chemical reactions are evaluated well. The methane conversation rates are about 0.36 and 0.35 which

Steam and CO2 reforming of methane over a Ru/ZrO2 catalyst

DEFF Research Database (Denmark)

Jakobsen, Jon Geest; Jørgensen, T.L.; Chorkendorff, Ib

2010-01-01

The kinetics of methane steam reforming over a Ru/ZrO2 catalyst was studied at 1.3 bar total pressure and in the temperature range 425-575 degrees C. These data were fitted by combining a reactor model with a series of kinetic models. The best fit was obtained by a model with methane dissociative...... adsorption as the rate limiting step and with CO and H adspecies partly blocking the active sites. The Ru/ZrO2 catalyst was characterized by TEM and H-2 chemisorption. By comparison of ex situ and in situ TEM, it is evident that Ru particles with diameters of...

Effects of adding lanthanum to Ni/ZrO2 catalysts on ethanol steam reforming

International Nuclear Information System (INIS)

Profeti, Luciene Paula Roberto; Habitzheuter, Filipe; Assaf, Elisabete Moreira

2012-01-01

The catalytic performance of Ni/ZrO 2 catalysts loaded with different lanthanum content for steam reforming of ethanol was investigated. Catalysts were characterized by BET surface area, X-ray diffraction, UV-vis spectroscopy, temperature programmed reduction, and X-ray absorption fine structure techniques. Results showed that lanthanum addition led to an increase in the degree of reduction of both NiO and nickel surface species interacting with the support, due to the higher dispersion effect. The best catalytic performance at 450 deg C was found for the Ni/12LZ catalyst, which exhibited an effluent gaseous mixture with the highest H 2 yield. (author)

Hydrogen production by steam reforming of liquefied natural gas over a nickel catalyst supported on mesoporous alumina xerogel

Science.gov (United States)

Seo, Jeong Gil; Youn, Min Hye; Cho, Kyung Min; Park, Sunyoung; Song, In Kyu

Mesoporous alumina xerogel (A-SG) is prepared by a sol-gel method for use as a support for a nickel catalyst. The Ni/A-SG catalyst is then prepared by an impregnation method, and is applied to hydrogen production by steam reforming of liquefied natural gas (LNG). The effect of the mesoporous alumina xerogel support on the catalytic performance of Ni/A-SG catalyst is investigated. For the purpose of comparison, a nickel catalyst supported on commercial alumina (A-C) is also prepared by an impregnation method (Ni/A-C). Both the hydroxyl-rich surface and the electron-deficient sites of the A-SG support enhance the dispersion of the nickel species on the support during the calcination step. The formation of the surface nickel aluminate phase in the Ni/A-SG catalyst remarkably increases the reducibility and stability of the catalyst. Furthermore, the high-surface area and the well-developed mesoporosity of the Ni/A-SG catalyst enhance the gasification of surface hydrocarbons that are adsorbed in the reaction. In the steam reforming of LNG, the Ni/A-SG catalyst exhibits a better catalytic performance than the Ni/A-C catalyst in terms of LNG conversion and hydrogen production. Moreover, the Ni/A-SG catalyst shows strong resistance toward catalyst deactivation.

Novel Auto thermal Reforming Process for Pure Hydrogen Production

International Nuclear Information System (INIS)

Chen, Z.; Elnashaie, S.S.E.H.

2004-01-01

Steam reforming of heptane for hydrogen production is investigated in a novel Circulating Fluidized Bed Membrane Reformer-Regenerator system (CFBMRR) utilizing a number of hydrogen and oxygen selective membranes. It is shown that although the amount of carbon deposition is significant, the effect on catalyst deactivation is negligible due to the large solid to gas mass feed ratio and the continuous catalyst regeneration in the system. The combustion of the deposited carbon in the catalyst regenerator supplies the heat needed for the endothermic steam reforming as well as the combustion of flammable gases from the riser reformer. Auto thermal operation is achievable for the entire adiabatic reformer-regenerator system when the exothermic heat generated from the regenerator is sufficient to compensate the endothermic heat consumed in the reformer. Multiplicity of the steady states exists in the range of steam to carbon feed ratio of 1.4442.251 mol/mol. The novel configuration has the potential advantages not only with respect to hydrogen production but also energy minimization

Synthesis and Activity Test of Cu/ZnO/Al2O3 for the Methanol Steam Reforming as a Fuel Cell’s Hydrogen Supplier

Directory of Open Access Journals (Sweden)

IGBN Makertihartha

2009-05-01

Full Text Available The synthesis of hydrogen from hydrocarbons through the steam reforming of methanol on Cu/ZnO/Al2O3 catalyst has been investigated. This process is assigned to be one of the promising alternatives for fuel cell hydrogen process source. Hydrogen synthesis from methanol can be carried out by means of methanol steam reforming which is a gas phase catalytic reaction between methanol and water. In this research, the Cu/ZnO/Al2O3 catalyst prepared by the dry impregnation was used. The specific surface area of catalyst was 194.69 m2/gram.The methanol steam reforming (SRM reaction was carried out by means of the injection of gas mixture containing methanol and water with 1:1.2 mol ratio and 20-90 mL/minute feed flow rate to a fixed bed reactor loaded by 1 g of catalyst. The reaction temperature was 200-300 °C, and the reactor pressure was 1 atm. Preceding the reaction, catalyst was reduced in the H2/N2 mixture at 160 °C. This study shows that at 300 °C reaction temperature, methanol conversion reached 100% at 28 mL/minute gas flow rate. This conversion decreased significantly with the increase of gas flow rate. Meanwhile, the catalyst prepared for SRM was stable in 36 hours of operation at 260 °C. The catalyst exhibited a good stability although the reaction condition was shifted to a higher gas flow rate.

Promoting Effect of CeO2 Addition on Activity and Catalytic Stability in Steam Reforming of Methane over Ni/Al2O3

International Nuclear Information System (INIS)

Rakib, A.; Gennequin, C.; Ringot, S.; Aboukais, A.; Abi-Aad, E.; Dhainaut, T.

2011-01-01

Hydrogen production by steam reforming of methane was studied over Ni catalysts supported on CeO 2 , Al 2 O 3 and CeO 2 -Al 2 O 3 . These catalysts were prepared using the impregnation method and characterized by XRD. The effect of CeO2 promoter on the catalytic performance of Ni/Al 2 O 3 catalyst for methane steam reforming reaction was investigated. In fact, CeO 2 had a positive effect on the catalytic activity in this reaction. Experimental results demonstrated that Ni/CeO 2 -Al 2 O 3 catalyst showed excellent catalytic activity and high reaction performance. In addition, the effects of reaction temperature and metal content on the conversion of CH 4 and H 2 /CO ratio were also investigated. Results indicated that CH4 conversion increased significantly with the increase of the reaction temperature and metal content. (author)

Response Surface Methodology and Aspen Plus Integration for the Simulation of the Catalytic Steam Reforming of Ethanol

Directory of Open Access Journals (Sweden)

Bernay Cifuentes

2017-01-01

Full Text Available The steam reforming of ethanol (SRE on a bimetallic RhPt/CeO2 catalyst was evaluated by the integration of Response Surface Methodology (RSM and Aspen Plus (version 9.0, Aspen Tech, Burlington, MA, USA, 2016. First, the effect of the Rh–Pt weight ratio (1:0, 3:1, 1:1, 1:3, and 0:1 on the performance of SRE on RhPt/CeO2 was assessed between 400 to 700 °C with a stoichiometric steam/ethanol molar ratio of 3. RSM enabled modeling of the system and identification of a maximum of 4.2 mol H2/mol EtOH (700 °C with the Rh0.4Pt0.4/CeO2 catalyst. The mathematical models were integrated into Aspen Plus through Excel in order to simulate a process involving SRE, H2 purification, and electricity production in a fuel cell (FC. An energy sensitivity analysis of the process was performed in Aspen Plus, and the information obtained was used to generate new response surfaces. The response surfaces demonstrated that an increase in H2 production requires more energy consumption in the steam reforming of ethanol. However, increasing H2 production rebounds in more energy production in the fuel cell, which increases the overall efficiency of the system. The minimum H2 yield needed to make the system energetically sustainable was identified as 1.2 mol H2/mol EtOH. According to the results of the integration of RSM models into Aspen Plus, the system using Rh0.4Pt0.4/CeO2 can produce a maximum net energy of 742 kJ/mol H2, of which 40% could be converted into electricity in the FC (297 kJ/mol H2 produced. The remaining energy can be recovered as heat.

Effects of key factors on solar aided methane steam reforming in porous medium thermochemical reactor

International Nuclear Information System (INIS)

Wang, Fuqiang; Tan, Jianyu; Ma, Lanxin; Leng, Yu

2015-01-01

Highlights: • Effects of key factors on chemical reaction for solar methane reforming are studied. • MCRT and FVM method coupled with UDFs is used to establish numerical model. • Heat and mass transfer model coupled with thermochemical reaction is established. • LTNE model coupled with P1 approximation is used for porous matrix solar reactor. • A formula between H 2 production and conductivity of porous matrix is put forward. - Abstract: With the aid of solar energy, methane reforming process can save up to 20% of the total methane consumption. Monte Carlo Ray Tracing (MCRT) method and Finite Volume Method (FVM) combined method are developed to establish the heat and mass transfer model coupled with thermochemical reaction kinetics for porous medium solar thermochemical reactor. In order to provide more temperature information, local thermal non-equilibrium (LTNE) model coupled with P1 approximation is established to investigate the thermal performance of porous medium solar thermochemical reaction. Effects of radiative heat loss and thermal conductivity of porous matrix on temperature distribution and thermochemical reaction for solar driven steam methane reforming process are numerically studied. Besides, the relationship between hydrogen production and thermal conductivity of porous matrix are analyzed. The results illustrate that hydrogen production shows a 3 order polynomial relation with thermal conductivity of porous matrix

A Comparative Discussion of the Catalytic Activity and CO2-Selectivity of Cu-Zr and Pd-Zr (Intermetallic Compounds in Methanol Steam Reforming

Directory of Open Access Journals (Sweden)

Norbert Köpfle

2017-02-01

Full Text Available The activation and catalytic performance of two representative Zr-containing intermetallic systems, namely Cu-Zr and Pd-Zr, have been comparatively studied operando using methanol steam reforming (MSR as test reaction. Using an inverse surface science and bulk model catalyst approach, we monitored the transition of the initial metal/intermetallic compound structures into the eventual active and CO2-selective states upon contact to the methanol steam reforming mixture. For Cu-Zr, selected nominal stoichiometries ranging from Cu:Zr = 9:2 over 2:1 to 1:2 have been prepared by mixing the respective amounts of metallic Cu and Zr to yield different Cu-Zr bulk phases as initial catalyst structures. In addition, the methanol steam reforming performance of two Pd-Zr systems, that is, a bulk system with a nominal Pd:Zr = 2:1 stoichiometry and an inverse model system consisting of CVD-grown ZrOxHy layers on a polycrystalline Pd foil, has been comparatively assessed. While the CO2-selectivity and the overall catalytic performance of the Cu-Zr system is promising due to operando formation of a catalytically beneficial Cu-ZrO2 interface, the case for Pd-Zr is different. For both Pd-Zr systems, the low-temperature coking tendency, the high water-activation temperature and the CO2-selectivity spoiling inverse WGS reaction limit the use of the Pd-Zr systems for selective MSR applications, although alloying of Pd with Zr opens water activation channels to increase the CO2 selectivity.

Steam reforming as an alternative technique for treatment of oil sludge containing naturally occurring radioactive material

International Nuclear Information System (INIS)

Norasalwa Zakaria; Muhd Noor Muhd Yunus; Mohd Khairi Muhd Said; Mohamad Azman Che Mat Isa; Mohd Puad Abu

2004-01-01

Steam reforming treatment system is an innovative technology that holds a potential to treat mixed waste containing radioactive material. The system is utilizing the thermal heat of the superheated steam at 500 degree C to produce combustible gases and integrates it with ash melting at 1400 degree C for final destruction. In this system, liquids are evaporated, organics are converted into a hydrogen-rich gas, chlorinated compounds are converted in hydrochloric acid, and reactive chemicals in the waste containing radionuclide and heavy metals are converted into the stable product through ash melting dioxins and furans are not formed, but instead are destroyed in the reducing environment of the system. No secondary pollutants are produced from the system that requires subsequent treatment. The system is divided into three development stages, and currently the project is progressing at development stage 1. This project is an entailment of a concentrated effort to solve oil sludge containing radioactive material treatment issue. (Author)

Preparation and characterization of nickel catalysts supported on cerium for obtaining hydrogen from steam reforming of ethanol; Preparacao e caracterizacao de catalisadores de niquel suportados em ceria para obtencao de hidrogenio a partir da reforma a vapor do etanol

Energy Technology Data Exchange (ETDEWEB)

Urbaninho, A.B.; Bergamaschi, V.S.; Ferreira, J.C., E-mail: jcferrei@ipen.br [Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil). Centro de Células à Combustível e Hidrogênio

2016-07-01

The Ni/Ce catalysts for were prepared by co- precipitation method with a view to their use in steam reforming of ethanol to produce a hydrogen-rich gas mixture. The catalysts were characterized by scanning electron microscopy; x-ray dispersive Spectroscopy and surface area BET method. This paper proposes to prepare, characterize and test nickel catalyst supported on cerium in order to obtain a material with higher activity and selectivity of the catalyst using the steam reforming reaction of ethanol, by varying the reaction temperature, molar ratio water/ethanol and uptime. The catalytic tests were monitored by chemical analysis of syngas from steam reforming of ethanol using an analysis online by gas Chromatograph in the reactor. (author)

Method of preparing a catalyst suitable for steam reformation of hydrocarbons and for methane production. [German patent

Energy Technology Data Exchange (ETDEWEB)

Golebiowski, A; Romotowski, T; Hennel, W; Wroblewska-Wroblewska, T; Polanski, A; Janecki, Z; Paluch-Paluch, S

1977-05-26

A method of producing a nickel catalyst suitable for steam reformation and methane production is described which forms a permanent bond with the inner surface of an externally heated metal tube, e.g. a heat exchanger tube. To begin with, a metal sponge with good adhesion to the metal tube is produced on the basis of a metallic powder of the metal group which is treated by a conventional calcination process. The metal sponge is then covered with a metal oxide which is not reduced under reformation conditions, e.g. aluminium oxide, by wetting the metal sponge with aluminium nitrate and repeated calcination. Wetting and calcination are repeated twice, and the calcination temperature is lower each time in the range between 400 and 1200/sup 0/C. The activated nickel is there deposited by wetting with a nickel salt solution and subsequent calcination.

Deactivation Studies of Rh/Ce0.8Zr0.2O2 Catalysts in Low Temperature Ethanol Steam Reforming

Energy Technology Data Exchange (ETDEWEB)

Platon, Alex; Roh, Hyun-Seog; King, David L.; Wang, Yong

2007-10-30

Rapid deactivation of Rh/Ce0.8Zr0.2O2 catalysts in low temperature ethanol steam reforming was studied. A significant build-up of carbonaceous intermediate, instead of carbon deposit, was observed at a lower reaction temperature which was attributed to the rapid catalyst deactivation. Co-feed experiments indicated that acetone and ethylene caused more severe catalyst deactivation than other oxygenates such as acidic acid and acetaldehyde.

Results from integral tests of single reformer tubes under simulated nuclear reactor conditions

International Nuclear Information System (INIS)

Decken, C.B. von der; Fedders, H.; Harth, R.; Hoehlein, B.; Riensche, E.

1980-01-01

The possibility of supplying high temperature heat from a HTGR for process application is being investigated at some places in the world. In all programmes or projects existing with respect to this application, the endothermic steam reforming of methane is one main step in the transmission of heat produced by nuclear fission to different chemical processes. The KFA is involved in the two German projects PNP - Prototypanlage Nukleare Prozesswaerme (Prototype-plant Nuclear Process-heat), and NFE -Nukleare Fernenergie (Long Distance Energy Transport). In a HTGR, helium generally serves as reactor coolant. It transports the heat from the core to the different components which take over this heat for various purposes. In case of arranging a steam reformer in the helium circuit, it is necessary for economic reasons to reach very high temperatures. In the two German projects mentioned above, the helium temperature at HTGR core outlet is determined to 950 0 C. Thus the main design data for a steam reformer supplied by heat from a HTGR are maximum helium temperature 950 0 C, helium pressure 40 bar. By an extensive utilization of the available advanced conventional steam reforming technology, the helium heated steam reformer design is using normal steam reforming tubes arranged in compact bundles

Performance evaluation of the DCMD desalination process under bench scale and large scale module operating conditions

KAUST Repository

Francis, Lijo

2014-04-01

The flux performance of different hydrophobic microporous flat sheet commercial membranes made of poly tetrafluoroethylene (PTFE) and poly propylene (PP) was tested for Red Sea water desalination using the direct contact membrane distillation (DCMD) process, under bench scale (high δT) and large scale module (low δT) operating conditions. Membranes were characterized for their surface morphology, water contact angle, thickness, porosity, pore size and pore size distribution. The DCMD process performance was optimized using a locally designed and fabricated module aiming to maximize the flux at different levels of operating parameters, mainly feed water and coolant inlet temperatures at different temperature differences across the membrane (δT). Water vapor flux of 88.8kg/m2h was obtained using a PTFE membrane at high δT (60°C). In addition, the flux performance was compared to the first generation of a new locally synthesized and fabricated membrane made of a different class of polymer under the same conditions. A total salt rejection of 99.99% and boron rejection of 99.41% were achieved under extreme operating conditions. On the other hand, a detailed water characterization revealed that low molecular weight non-ionic molecules (ppb level) were transported with the water vapor molecules through the membrane structure. The membrane which provided the highest flux was then tested under large scale module operating conditions. The average flux of the latter study (low δT) was found to be eight times lower than that of the bench scale (high δT) operating conditions.

Performance evaluation of the DCMD desalination process under bench scale and large scale module operating conditions

KAUST Repository

Francis, Lijo; Ghaffour, NorEddine; Alsaadi, Ahmad Salem; Nunes, Suzana Pereira; Amy, Gary L.

2014-01-01

The flux performance of different hydrophobic microporous flat sheet commercial membranes made of poly tetrafluoroethylene (PTFE) and poly propylene (PP) was tested for Red Sea water desalination using the direct contact membrane distillation (DCMD) process, under bench scale (high δT) and large scale module (low δT) operating conditions. Membranes were characterized for their surface morphology, water contact angle, thickness, porosity, pore size and pore size distribution. The DCMD process performance was optimized using a locally designed and fabricated module aiming to maximize the flux at different levels of operating parameters, mainly feed water and coolant inlet temperatures at different temperature differences across the membrane (δT). Water vapor flux of 88.8kg/m2h was obtained using a PTFE membrane at high δT (60°C). In addition, the flux performance was compared to the first generation of a new locally synthesized and fabricated membrane made of a different class of polymer under the same conditions. A total salt rejection of 99.99% and boron rejection of 99.41% were achieved under extreme operating conditions. On the other hand, a detailed water characterization revealed that low molecular weight non-ionic molecules (ppb level) were transported with the water vapor molecules through the membrane structure. The membrane which provided the highest flux was then tested under large scale module operating conditions. The average flux of the latter study (low δT) was found to be eight times lower than that of the bench scale (high δT) operating conditions.

Design principles of an integrated natural gas steam reformer for stationary PEMFC systems; Auslegungsprinzipien eines integrierten Erdgas-Dampfreformers fuer stationaere PEM-Brennstoffzellen-Systeme

Energy Technology Data Exchange (ETDEWEB)

Grosser, K.

2006-09-05

The function, efficiency and economic efficiency of fuel cell systems are defined by various influencing factors, especially in the case of hydrogen production by steam reforming of natural gas. The dissertation describes the design of integrated natural gas steam reformers for PEM fuel cell systems in the electric power range of 1- 10 kW; the influencing factors of the process are investigated and weighted. Design principles are derived from which optimum operating parameters can be defined and which can be used for designing a multitude of components. [German] Die Funktionsfaehigkeit, der Wirkungsgrad und die Wirtschaftlichkeit von Brennstoffzellen-Systemen werden insbesondere bei der Wasserstofferzeugung durch Erdgas-Dampfreformierung durch verschiedene Einflussfaktoren bestimmt. In dieser Dissertation werden die Methodik der Auslegung integrierter Erdgas-Dampfreformer fuer PEM-Brennstoffzellen-Systeme im elektrischen Leistungsbereich von 1-10 kW beschrieben und die prozessbestimmenden Einflussfaktoren untersucht und gewichtet. Daraus werden Auslegungsprinzipien abgeleitet, mit denen sich die optimalen Betriebsparameter ermitteln lassen und die zur konstruktiven Gestaltung einer Vielzahl von Anlagenteilen genutzt werden koennen.

Co-Fe-Si Aerogel Catalytic Honeycombs for Low Temperature Ethanol Steam Reforming

Directory of Open Access Journals (Sweden)

Montserrat Domínguez

2012-09-01

Full Text Available Cobalt talc doped with iron (Fe/Co~0.1 and dispersed in SiO2 aerogel was prepared from silica alcogel impregnated with metal nitrates by supercritical drying. Catalytic honeycombs were prepared following the same procedure, with the alcogel synthesized directly over cordierite honeycomb pieces. The composite aerogel catalyst was characterized by X-ray diffraction, scanning electron microscopy, focus ion beam, specific surface area and X-ray photoelectron spectroscopy. The catalytic layer is about 8 µm thick and adheres well to the cordierite support. It is constituted of talc layers of about 1.5 µm × 300 nm × 50 nm which are well dispersed and anchored in a SiO2 aerogel matrix with excellent mass-transfer properties. The catalyst was tested in the ethanol steam reforming reaction, aimed at producing hydrogen for on-board, on-demand applications at moderate temperature (573–673 K and pressure (1–7 bar. Compared to non-promoted cobalt talc, the catalyst doped with iron produces less methane as byproduct, which can only be reformed at high temperature, thereby resulting in higher hydrogen yields. At 673 K and 2 bar, 1.04 NLH2·mLEtOH(l−1·min−1 are obtained at S/C = 3 and W/F = 390 g·min·molEtOH−1.

Environmental data from laboratory- and bench-scale Pressurized Fluidized-Bed Hydroretorting of Eastern oil shale

Energy Technology Data Exchange (ETDEWEB)

Mensinger, M.C.; Rue, D.M.; Roberts, M.J.

1991-01-01

As part of a 3-year program to develop the Pressurized Fluidized-Bed Hydroretorting (PFH) Process for Eastern oil shales, IGT conducted tests in laboratory-scale batch and continuous units as well as a 45-kg/h bench-scale unit to generate a data base for 6 Eastern shales. Data were collected during PFH processing of raw Alabama and Indiana shales and a beneficiated Indiana shale for environmental mitigation analyses. The data generated include trace element analyses of the raw feeds and spent shales, product oils, and sour waters. The sulfur compounds present in the product gas and trace components in the sour water were also determined. In addition, the leaching characteristics of the feed and residue solids were determined. The data obtained were used to evaluate the environmental impact of a shale processing plant based on the PFH process. This paper presents the environmental data obtained from bench-scale tests conducted during the program.

Environmental data from laboratory- and bench-scale Pressurized Fluidized-Bed Hydroretorting of Eastern oil shale

Energy Technology Data Exchange (ETDEWEB)

Mensinger, M.C.; Rue, D.M.; Roberts, M.J.

1991-12-31

As part of a 3-year program to develop the Pressurized Fluidized-Bed Hydroretorting (PFH) Process for Eastern oil shales, IGT conducted tests in laboratory-scale batch and continuous units as well as a 45-kg/h bench-scale unit to generate a data base for 6 Eastern shales. Data were collected during PFH processing of raw Alabama and Indiana shales and a beneficiated Indiana shale for environmental mitigation analyses. The data generated include trace element analyses of the raw feeds and spent shales, product oils, and sour waters. The sulfur compounds present in the product gas and trace components in the sour water were also determined. In addition, the leaching characteristics of the feed and residue solids were determined. The data obtained were used to evaluate the environmental impact of a shale processing plant based on the PFH process. This paper presents the environmental data obtained from bench-scale tests conducted during the program.

Advanced design of fast reactor-membrane reformer (FR-MR)

International Nuclear Information System (INIS)

Tashimo, M.; Hori, I.; Yasuda, I.; Shirasaki, Y.; Kobayashi, K.

2004-01-01

A new plant concept of nuclear-produced hydrogen is being studied using a Fast Reactor-Membrane Reformer (FR-MR). The conventional steam methane reforming (SMR) system is a three-stage process. The first stage includes the reforming, the second contains a shift reaction and the third is the separation process. The reforming process requires high temperatures of 800 ∼ 900 deg C. The shift process generates heat and is performed at around 200 deg C. The membrane reforming has only one process stage under a nonequilibrium condition by removing H2 selectively through a membrane tube. The steam reforming temperature can be decreased from 800 deg C to 550 deg C, which is a remarkable benefit offered by the non-equilibrium condition. With this new technology, the reactor type can be changed from a High Temperature Gas-cooled Reactor (HTGR) to a Fast Reactor (FR). A Fast Reactor-Membrane Reformer (FR-MR) is composed of a nuclear plant and a hydrogen plant. The nuclear plant is a sodium-cooled Fast Reactor with mixed oxide fuel and with a power of 240 MWt. The heat transport system contains two circuits, the primary circuit and the secondary circuit. The membrane reformer units are set in the secondary circuit. The heat, supplied by the sodium, can produce 200 000 Nm 3 /h by 2 units. There are two types of membranes. One is made of Pd another one (advanced) is made of, for example V, or Nb. The technology for the Pd membrane is already established in a small scale. The non-Pd type is expected to improve the performance. (author)

Performance study of protective clothing against hot water splashes: from bench scale test to instrumented manikin test.

Science.gov (United States)

Lu, Yehu; Song, Guowen; Wang, Faming

2015-03-01

Hot liquid hazards existing in work environments are shown to be a considerable risk for industrial workers. In this study, the predicted protection from fabric was assessed by a modified hot liquid splash tester. In these tests, conditions with and without an air spacer were applied. The protective performance of a garment exposed to hot water spray was investigated by a spray manikin evaluation system. Three-dimensional body scanning technique was used to characterize the air gap size between the protective clothing and the manikin skin. The relationship between bench scale test and manikin test was discussed and the regression model was established to predict the overall percentage of skin burn while wearing protective clothing. The results demonstrated strong correlations between bench scale test and manikin test. Based on these studies, the overall performance of protective clothing against hot water spray can be estimated on the basis of the results of the bench scale hot water splashes test and the information of air gap size entrapped in clothing. The findings provide effective guides for the design and material selection while developing high performance protective clothing. Published by Oxford University Press on behalf of the British Occupational Hygiene Society 2014.

The agnion Heatpipe-Reformer - operating experiences and evaluation of fuel conversion and syngas composition

Energy Technology Data Exchange (ETDEWEB)

Gallmetzer, Georg; Ackermann, Pascal [Highterm Research GmbH, Hettenshausen (Germany); Schweiger, Andreas; Kienberger, Thomas [Highterm Research GmbH, Graz (Austria); Groebl, Thomas; Walter, Heimo [Technische Universitaet Wien, Institut fuer Energietechnik und Thermodynamik, Wien (Austria); Zankl, Markus; Kroener, Martin [Agnion Technologies GmbH, Hettenshausen (Germany)

2012-09-15

Fluidized bed gasification of solid fuels is considered as one of the core technologies for future sustainable energy supply. Whereas autothermal oxygen-driven gasification is applied in large-scale substitute natural gas (SNG) and Fischer-Tropsch (FT) plants or small-scale combined heat and power (CHP) plants, the allothermal steam-reforming process of the agnion Heatpipe-Reformer is designed for cost- and fuel-efficient syngas generation at small scales for distributed applications. The Heatpipe-Reformer's pressurized syngas generation provides a number of benefits for SNG, biomass to liquid (BTL) and CHP applications. A modified gas engine concept uses the pressurized and hydrogen-rich syngas for increased performance and tar tolerance at decreased capital expenses. Agnion has installed and operated a 500-kW thermal input pilot plant in Pfaffenhofen, Germany, over the last 2 years, showing stable operation over a variety of operating points. The syngas composition has been measured at values expected by thermodynamic models. An influence of the steam-to-fuel ratio and reformer temperature was observed. Tar and sulphur contents have been monitored and correlated to operation parameters, showing influences on stoichiometry and carbon conversion. The mass and energy streams of the plant were balanced. One of the main observations in the monitoring programme is the fact that syngas output, efficiency and syngas quality correlate to high values if the carbon conversion is high. Carbon conversion rates and cold gas efficiencies are comparably high in respect to today's processes, promising economic and fuel-efficient operation of the Heatpipe-Reformer applications. (orig.)

Hydrogen production from coal using a nuclear heat source

International Nuclear Information System (INIS)

Quade, R.N.

1977-01-01

A strong candidate for hydrogen production in the intermediate time frame of 1990 to 1995 is a coal-based process using a high-temperature gas-cooled reactor (HTGR) as a heat source. Expected process efficiencies in the range of 60 to 70% are considerably higher than all other hydrogen production processes except steam reforming of a natural gas - a feedstock which may not be available in large quantities in this time frame. The process involves the preparation of a coal liquid, hydrogasification of that liquid, and steam reforming of the resulting gaseous or light liquid product. Bench-scale experimental work on the hydrogasification of coal liquids is being carried out. A study showing process efficiency and cost of hydrogen vs nuclear reactor core outlet temperature has been completed and shows diminishing returns at process temperatures above about 1500 0 F. (author)

Experimental analysis of an autothermal reformer for automotive purposes

International Nuclear Information System (INIS)

Caners, C.; Peppley, B.; Harrison, S.; Oosthuizen, P.

2004-01-01

This paper describes the experimental analysis, concomitant with modeling research, to determine improved operating parameters and design of an autothermal reformer. The reformer, utilizing both partial oxidation and steam reforming reactions, along with the water gas shift phenomena is well suited for the mobile application of transportation. This is due to the novel geometry of the autothermal reformer, which seeks to improve the heat transfer characteristics of the process, whereby the exothermic partial oxidation reaction provides the heat energy required to drive the steam reforming reaction, to the point of a thermally neutral system. The paper will present data from the experimental results of reforming iso-octane as a surrogate for gasoline in the form of reformate composition, iso-octane conversion percentages and efficiencies in terms of hydrogen realized per mol of fuel input. (author)

Draft, development and optimization of a fuel cell system for residential power generation with steam reformer; Entwurf, Aufbau und Optimierung eines PEM-Brennstoffzellensystems zur Hausenergieversorgung mit Dampfreformer

Energy Technology Data Exchange (ETDEWEB)

Brandt, H

2006-05-17

The first development cycle of a residential power generation system is described. A steam reformer was chosen to produce hydrogen out of natural gas. After carbon monoxide purification with a preferential oxidation (PrOx) unit the hydrogen rich reformat gas is feed to the anode of the PEM-fuel cell, where due to the internal reaction with air oxygen form the cathode side water, heat and electricity is produced. Due to an incomplete conversion the anode off gas contains hydrogen and residual methane, which is feed to the burner of the steam reformer to reduce the needed amount of external fuel to heat the steam reformer. To develop the system the components are separately investigated and optimized in their construction or operation to meet the system requirements. After steady state and dynamic characterization of the components they were coupled one after another to build the system. To operate the system a system control was developed to operate and characterize this complex system. After characterization the system was analyzed for further optimization. During the development of the system inventions like a water cooled PrOx, an independent fuel cell controller or a burner for anodic off gas recirculation were made. The work gives a look into the interactions between the components and allows to understand the problems by coupling such components. (orig.)

Dynamic modeling of a three-stage low-temperature ethanol reformer for fuel cell application

Energy Technology Data Exchange (ETDEWEB)

Garcia, Vanesa M; Serra, Maria [Institut de Robotica i Informatica Industrial (CSIC-UPC), Llorens i Artigas 4-6, 08028 Barcelona (Spain); Lopez, Eduardo; Llorca, Jordi [Institut de Tecniques Energetiques, Universitat Politecnica de Catalunya, Diagonal 647, ed. ETSEIB, 08028 Barcelona (Spain)

2009-07-01

A low-temperature ethanol reformer based on a cobalt catalyst for the production of hydrogen has been designed aiming the feed of a fuel cell for an autonomous low-scale power production unit. The reformer comprises three stages: ethanol dehydrogenation to acetaldehyde and hydrogen over SnO{sub 2} followed by acetaldehyde steam reforming over Co(Fe)/ZnO catalyst and water gas shift reaction. Kinetic data have been obtained under different experimental conditions and a dynamic model has been developed for a tubular reformer loaded with catalytic monoliths for the production of the hydrogen required to feed a 1 kW PEMFC. (author)

A novel bench-scale column assay to investigate site-specific nitrification biokinetics in biological rapid sand filters

DEFF Research Database (Denmark)

Tatari, Karolina; Smets, Barth F.; Albrechtsen, Hans-Jørgen

2013-01-01

A bench-scale assay was developed to obtain site-specific nitrification biokinetic information from biological rapid sand filters employed in groundwater treatment. The experimental set-up uses granular material subsampled from a full-scale filter, packed in a column, and operated with controlled...

Steam Reforming of CH4 Using Ni- Substituted Pyrochlore Catalysts

Science.gov (United States)

Haynes, Daniel J.

The steam reforming of methane (SMR) continues to remain an important industrial reaction for large-scale production of H2 as well as synthesis gas mixtures which can be used for the production of useful chemicals (e.g. methanol). Although SMR is a rather mature technology, traditional nickel based catalysts used industrially are subjected to severe temperatures and reaction conditions, which lead to irreversible activity loss through sintering, support collapse, and carbon formation. Pyrochlore-based mixed oxide have been identified as refractory materials that can be modified through the substitution of catalytic metals and other promoting species into the structure to mitigate these issues causing deactivation. For this study, a lanthanum zirconate pyrochlore catalyst was substituted with Ni to determine whether the oxide structure could effectively stabilize the activity of the catalytic metal during the SMR. The effect of different variables including calcination temperature, a comparison of a substituted versus supported Ni pyrochlore catalyst, Ni weight loading, and Sr promotion have been evaluated to determine the location of the Ni in the structure, and their effect on catalytic behavior. It was revealed that the effect of calcination temperature on a 6wt% Ni substituted pyrochlore produced by the Pechini method demonstrated very little Ni was soluble in the pyrochlore lattice. It was further revealed that by XRD, TEM, and atom probe tomography that, despite the metal loading, Ni exsolves from the structure upon crystallization of the pyrochlore at 700°C, and forms NiO at the surface and grain boundaries. An additional separate La2ZrNiO6 perovskite phase also began to form at higher temperatures (>800°C). Increasing calcination temperature was found to lead to slight sintering of the NiO at the surface, which made the NiO more reducible. Meanwhile decreasing the Ni weight loading was found to produce a lower reduction temperature due to the presence of

Hydrogen production with a solar steam–methanol reformer and colloid nanocatalyst

KAUST Repository

Lee, Ming-Tsang

2010-01-01

In the present study a small steam-methanol reformer with a colloid nanocatalyst is utilized to produce hydrogen. Radiation from a focused continuous green light laser (514 nm wavelength) is used to provide the energy for steam-methanol reforming. Nanocatalyst particles, fabricated by using pulsed laser ablation technology, result in a highly active catalyst with high surface to volume ratio. A small novel reformer fabricated with a borosilicate capillary is employed to increase the local temperature of the reformer and thereby increase hydrogen production. The hydrogen production output efficiency is determined and a value of 5% is achieved. Experiments using concentrated solar simulator light as the radiation source are also carried out. The results show that hydrogen production by solar steam-methanol colloid nanocatalyst reforming is both feasible and promising. © 2009 Professor T. Nejat Veziroglu.

Genifuel Hydrothermal Processing Bench Scale Technology Evaluation Project (WE&RF Report LIFT6T14)

Science.gov (United States)

Hydrothermal Liquefaction (HTL) and Catalytic Hydrothermal Gasification (CHG) proof-of-concept bench-scale tests were performed to assess the potential of the Genifuel hydrothermal process technology for handling municipal wastewater sludge. HTL tests were conducted at 300-350◦C ...

Various Transport Phenomena and Modeling in a Methane Reformer Duct for PEMFCs

International Nuclear Information System (INIS)

Jinliang Yuan; Fuan Ren; Jinliang Yuan; Bengt Sunden

2006-01-01

There are various physical processes (such as mass, heat and momentum transport) integrated with catalytic chemical reactions in a methane steam reforming duct. It is often found that endothermic and exothermic reactions in the ducts are strongly coupled by heat transfer from adjacent catalytic combustion ducts. In this paper, a three-dimensional calculation method is developed to simulate and analyze steam reforming of methane, and the effects on various transport processes in a steam reforming duct. The reformer conditions such as mass balances associated with the reforming reactions and gas permeation to/from the porous catalyst layer are applied in the analysis. The predicted results are presented and discussed for a composite duct consisting of a porous catalyst reaction area, the gas flow duct and solid layers. Parametric studies are conducted and the results show that the variables, such as fuel reformer temperatures and catalyst loadings, have significant effects on the transport processes and reformer performance. (authors)

Bench Scale Development and Testing of Aerogel Sorbents for CO₂ Capture Final Technical Report

Energy Technology Data Exchange (ETDEWEB)

Begag, Redouane [Aspen Aerogels, Northborough, MA (United States)

2017-03-30

The primary objective of this project was scaling up and evaluating a novel Amine Functionalized Aerogel (AFA) sorbent in a bench scale fluidized bed reactor. The project team (Aspen Aerogels, University of Akron, ADA-ES, and Longtail Consulting) has carried out numerous tests and optimization studies to demonstrate the CO₂ capture performance of the AFA sorbent in all its forms: powder, pellet, and bead. The CO₂ capture target performance of the AFA sorbent (all forms) were set at > 12 wt.% and > 6 wt.% for total and working CO₂ capacity, respectively (@ 40 °C adsorption / 100 – 120 °C desorption). The optimized AFA powders outperformed the performance targets by more than 30%, for the total CO₂ capacity (14 - 20 wt.%), and an average of 10 % more for working CO₂ capacity (6.6 – 7.0 wt.%, and could be as high as 9.6 wt. % when desorbed at 120 °C). The University of Akron developed binder formulations, pellet production methods, and post treatment technology for increased resistance to attrition and flue gas contaminants. In pellet form the AFA total CO₂ capacity was ~ 12 wt.% (over 85% capacity retention of that of the powder), and there was less than 13% degradation in CO₂ capture capacity after 20 cycles in the presence of 40 ppm SO₂. ADA-ES assessed the performance of the AFA powder, pellet, and bead by analyzing sorption isotherms, water uptake analysis, cycling stability, jet cup attrition and crush tests. At bench scale, the hydrodynamic and heat transfer properties of the AFA sorbent pellet in fluidized bed conditions were evaluated at Particulate Solid Research, Inc. (PSRI). After the process design requirements were completed, by Longtail Consulting LLC, a techno-economic analysis was achieved using guidance from The National Energy Technology Laboratory (NETL) report. This report provides the necessary framework to estimate costs for a temperature swing post

Hydrogen generation from biogenic and fossil fuels by autothermal reforming

Science.gov (United States)

Rampe, Thomas; Heinzel, Angelika; Vogel, Bernhard

Hydrogen generation for fuel cell systems by reforming technologies from various fuels is one of the main fields of investigation of the Fraunhofer ISE. Suitable fuels are, on the one hand, gaseous hydrocarbons like methane, propane but also, on the other hand, liquid hydrocarbons like gasoline and alcohols, e.g., ethanol as biogenic fuel. The goal is to develop compact systems for generation of hydrogen from fuel being suitable for small-scale membrane fuel cells. The most recent work is related to reforming according to the autothermal principle — fuel, air and steam is supplied to the reactor. Possible applications of such small-scale autothermal reformers are mobile systems and also miniature fuel cell as co-generation plant for decentralised electricity and heat generation. For small stand-alone systems without a connection to the natural gas grid liquid gas, a mixture of propane and butane is an appropriate fuel.

Bench scale studies: Ozonation as a potential treatment for waters contaminated with hydrocarbons or dioxins and furans

International Nuclear Information System (INIS)

Schaal, W.

1995-01-01

The objective of the bench scale studies was to examine the destruction efficiency and efficacy of ozone on chemicals of concern (COC's) commonly found in contaminated ground water and rhenoformer wash water. The ground water used in these tests contained aromatic petroleum hydrocarbons, chlorinated hydrocarbons, and mineral spirits. The rhenoformer wash water used in these tests contained a variety of dioxins (including 2,3,7,8-tetrachlorodibenzo-p-dioxin) and furans. Summaries are presented of the bench scale studies by describing the COCs, methodologies, test reactors, observations, and results. The summaries also detail which applications hold promise with respect to ozonation and which ones do not. Bench test results for the experiments in which aromatic petroleum hydrocarbons, chlorinated hydrocarbons, and mineral spirits where the COCs were relatively successful. Concentrations for the COCs ranging from 300 to 3,400 micrograms per liter (microg/L) were brought below levels specified for storm sewer discharge per the National Priority Discharge Elimination Systems (NPDES) permit requirements. Bench test results for the experiments in which dioxins and furans were the COCs were less promising and revealed that additional processes would have to be used in conjunction with ozonation to bring the concentration of COCs within the targeted ranges. It was realized, however, that the effectiveness and efficacy of ozonation were diminished by the presence of particulates, to which some of the dioxin and furan compounds adhered

Internal reforming of methane in solid oxide fuel cell systems

Science.gov (United States)

Peters, R.; Dahl, R.; Klüttgen, U.; Palm, C.; Stolten, D.

Internal reforming is an attractive option offering a significant cost reduction, higher efficiencies and faster load response of a solid oxide fuel cell (SOFC) power plant. However, complete internal reforming may lead to several problems which can be avoided with partial pre-reforming of natural gas. In order to achieve high total plant efficiency associated with low energy consumption and low investment costs, a process concept has been developed based on all the components of the SOFC system. In the case of anode gas recycling an internal steam circuit exists. This has the advantage that there is no need for an external steam generator and the steam concentration in the anode gas is reduced. However, anode gas recycling has to be proven by experiments in a pre-reformer and for internal reforming. The addition of carbon dioxide clearly shows a decrease in catalyst activity, while for temperatures higher than 1000 K hydrogen leads to an increase of the measured methane conversion rates.

Bench-Scale Evaluation of Peracetic Acid and Twin Oxide ™ as Disinfectants in Drinking Water

Science.gov (United States)

Chlorine is widely used as an inexpensive and potent disinfectant in the United States for drinking water. However, chlorine has the potential for forming carcinogenic and mutagenic disinfection by-products (DBPs). In this study, bench scale experiments were conducted at the U.S...

Bench- and field-scale evaluation of chromium and cadmium extraction by electrokinetics

International Nuclear Information System (INIS)

Gent, David B.; Bricka, R. Mark; Alshawabkeh, Akram N.; Larson, Steven L.; Fabian, Gene; Granade, Steve

2004-01-01

The results of bench-scale laboratory tests and in situ, pilot-scale demonstration of electrokinetic extraction of chromium and cadmium from contaminated soil are presented. The laboratory tests were conducted using 10 cm long samples under current density of 5 A/m 2 for 1200 h. Tests were conducted with and without citric acid amendment at the cathode. The results showed that citric acid improved extraction, especially in the sections near the cathode. However, processing was not enough to result in complete cleanup. The field demo was conducted at the Naval Air Weapon Station (NAWS), Point Mugu, California. Three cathodes were centered between six anodes. The anode-cathode spacing was 4.45 m (15 ft). Constant voltage of 60 V (∼13 V/m) was applied for 20 days and then was reduced to 45 V (10 V/m) for 6 months. Citric acid was used to maintain the cathode pH at 4. After 6 months of treatment, 78% of the soil volume has been cleared of chromium or treated to below natural background levels. The results also indicated that 70% of the soil between the electrodes had been cleared of cadmium contamination. A comparison between the bench-scale and field demo showed that the field process was more effective than the lab tests. This indicated that small sample size will induce a negative effect on the efficiency of the process due to an increased impact of the boundaries on the overall process

In situ remediation of hexavalent chromium with pyrite fines : bench scale demonstration

International Nuclear Information System (INIS)

Cathum, S.; Wong, W.P.; Brown, C.E.

2002-01-01

An in situ remediation technique for chromium contaminated soil with pyrite fines was presented. Past industrial activities and lack of disposal facilities have contributed to a serious problem dealing with chromium, which cannot be eliminated from the environment because it is an element. Both bench-scale and laboratory testing was conducted to confirm the efficiency of the proposed process which successfully converted Cr(VI) into Cr(III) in soil and water. Cr(III) is less toxic and immobile in the environment compared to Cr(VI) which moves freely in the soil matrix, posing a risk to the groundwater quality. pH in the range of 2.0 to 7.6 has no effect on the reactivity of pyrite towards Cr(VI). The optimization of the bench-scale treatment resulted in a large volume of chromium waste, mostly from the control experiments and column hydrology testing. These waste streams were treated according to municipal guidelines before disposal to the environment. Samples of chromium waste before and after treatment were analyzed. Cr (VI) was completely mineralized to below guideline levels. It was determined that several conditions, including contact time between pyrite and Cr(VI), are crucial for complete mineralization of Cr(VI). 13 refs., 8 tabs., 9 figs

Co/Zr substitution in a cerium-zirconium oxide by catalytic steam reforming of bio-ethanol

International Nuclear Information System (INIS)

Vargas, J.C.; Thomas, S.; Roger, A.C.; Kiennemann, A.; Vargas, J.C.

2006-01-01

This work deals with the production of hydrogen by bio-ethanol catalytic steam reforming. The aim is to develop a catalyst active in ethanol conversion, selective in hydrogen and resistant to deactivation, particularly those induced by the formation of carbon deposition. The metal-support interaction being one of the keys of this challenge, catalysts in which a transition metal is inserted into an oxide by a liquid synthesis method (by the precursor method) have been developed. The initial insertion of cobalt into a cerium oxide-zirconia structure presents the advantages to increase the redox properties of the host oxide and to allow a stable reduction of a cobalt part while favoring the metal-support interaction. (O.M.)

Direct Hysteresis Heating of Catalytically Active Ni–Co Nanoparticles as Steam Reforming Catalyst

DEFF Research Database (Denmark)

Mortensen, Peter Mølgaard; Engbæk, Jakob Soland; Vendelbo, Søren Bastholm

2017-01-01

We demonstrated a proof-of-concept catalytic steam reforming flow reactor system heated only by supported magnetic nickel–cobalt nanoparticles in an oscillating magnetic field. The heat transfer was facilitated by the hysteresis heating in the nickel–cobalt nanoparticles alone. This produced...... a sufficient power input to equilibrate the reaction at above 780 °C with more than 98% conversion of methane. The high conversion of methane indicated that Co-rich nanoparticles with a high Curie temperature provide sufficient heat to enable the endothermic reaction, with the catalytic activity facilitated...... by the Ni content in the nanoparticles. The magnetic hysteresis losses obtained from temperature-dependent hysteresis measurements were found to correlate well with the heat generation in the system. The direct heating of the catalytic system provides a fast heat transfer and thereby overcomes the heat...

Thermodynamic analysis of a membrane-assisted chemical looping reforming reactor concept for combined H2 production and CO2 capture

NARCIS (Netherlands)

Medrano Jimenez, J.A.; Spallina, V.; Sint Annaland, van M.; Gallucci, F.

2014-01-01

There is great consensus that hydrogen will become an important energy carrier in the future. Currently, hydrogen is mainly produced by steam reforming of natural gas/methane on large industrial scale or by electrolysis of water when high-purity hydrogen is needed for small-scale hydrogen plants.

Exergoeconomic analysis of small-scale biomass steam cogeneration

Energy Technology Data Exchange (ETDEWEB)

Rodriguez Sotomonte, Cesar Adolfo; Lora, Electo Eduardo Silva [Universidade Federal de Itajuba, MG (Brazil)], e-mails: c.rodriguez32@unifei.edu.br, electo@unifei.edu.br; Venturini, Osvaldo Jose; Escobar, Jose Carlos [Universidad Federal de Itajuba, MG (Brazil)], e-mail: osvaldo@unifei.edu.br

2010-07-01

The principal objective of this work is to develop a calculation process, based on the second law of thermodynamics, for evaluating the thermoeconomic potential of a small steam cogeneration plant using waste from pulp processing and/or sawmills as fuel. Four different configurations are presented and assessed. The exergetic efficiency of the cycles that use condensing turbines is found to be around 11%, which has almost 3 percent higher efficiency than cycles with back pressure turbines. The thermoeconomic equations used in this paper estimated the production costs varying the fuel price. The main results show that present cost of technologies in a small-scale steam cycle cogeneration do not justify the implementation of more efficient systems for biomass prices less than 100 R$/t. (author)

Domestic Wastewater Reuse in Concrete Using Bench-Scale Testing and Full-Scale Implementation

Directory of Open Access Journals (Sweden)

Ayoup M. Ghrair

2016-08-01

Full Text Available Demand for fresh water by the construction sector is expected to increase due to the high increase in the growth of construction activities in Jordan. This study aims to evaluate the potential of scale-up of the application of treated domestic wastewater in concrete from bench-scale to a full-scale. On the lab scale, concrete and mortar mixes using Primary and Secondary Treated Wastewater (PTW, STW and Distilled Water (DW were cast and tested after various curing ages (7, 28, 120, and 200 days. Based on wastewater quality, according to IS 456-2000, the STW is suitable for mortar and concrete production. Mortar made with STW at curing time up to 200 days has no significant negative effect on the mortar’s compressive strength. Conversely, the PTW exceeded the maximum permissible limits of total organic content and E coli. for concrete mixing-water. Using PTW results, a significant increase in the initial setting time of up to 16.7% and a decrease in the concrete workability are observed. In addition, using PTW as mixing water led to a significant reduction in the compressive strength up to 19.6%. The results that came out from scaling up to real production operation of ready-mix concrete were in harmony with the lab-scale results.

The application of inelastic neutron scattering to investigate the steam reforming of methane over an alumina-supported nickel catalyst

International Nuclear Information System (INIS)

McFarlane, Andrew R.; Silverwood, Ian P.; Norris, Elizabeth L.; Ormerod, R. Mark; Frost, Christopher D.; Parker, Stewart F.; Lennon, David

2013-01-01

Highlights: • Inelastic neutron scattering has been used to investigate a Ni/alumina catalyst. • The extent of hydrogen retention by the catalyst has been determined. • Filamentous carbon is identified as a by-product. - Abstract: An alumina-supported nickel catalyst, previously used in methane reforming experiments employing CO 2 as the oxidant, is applied here in the steam reforming variant of the process. Micro-reactor experiments are used to discern an operational window compatible with sample cells designed for inelastic neutron scattering (INS) experiments. INS spectra are recorded after 6 h reaction of a 1:1 mixture of CH 4 and H 2 O at 898 K. Weak INS spectra are observed, indicating minimal hydrogen retention by the catalyst in this operational regime. Post-reaction, the catalyst is further characterised by powder X-ray diffraction, transmission electron microscopy and Raman scattering. In a comparable fashion to that seen for the ‘dry’ reforming experiments, the catalyst retains substantial quantities of carbon in the form of filamentous coke. The role for hydrogen incorporation by the catalyst is briefly considered

The application of inelastic neutron scattering to investigate the steam reforming of methane over an alumina-supported nickel catalyst

Energy Technology Data Exchange (ETDEWEB)

McFarlane, Andrew R.; Silverwood, Ian P. [School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow G12 8QQ (United Kingdom); Norris, Elizabeth L.; Ormerod, R. Mark [Department of Chemistry, School of Physical and Geographical Sciences, Keele University, Staffs ST5 5BG (United Kingdom); Frost, Christopher D.; Parker, Stewart F. [ISIS Facility, STFC Rutherford Appleton Laboratory, Chilton, Didcot, Oxon OX11 0QX (United Kingdom); Lennon, David, E-mail: David.Lennon@glasgow.ac.uk [School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow G12 8QQ (United Kingdom)

2013-12-12

Highlights: • Inelastic neutron scattering has been used to investigate a Ni/alumina catalyst. • The extent of hydrogen retention by the catalyst has been determined. • Filamentous carbon is identified as a by-product. - Abstract: An alumina-supported nickel catalyst, previously used in methane reforming experiments employing CO{sub 2} as the oxidant, is applied here in the steam reforming variant of the process. Micro-reactor experiments are used to discern an operational window compatible with sample cells designed for inelastic neutron scattering (INS) experiments. INS spectra are recorded after 6 h reaction of a 1:1 mixture of CH{sub 4} and H{sub 2}O at 898 K. Weak INS spectra are observed, indicating minimal hydrogen retention by the catalyst in this operational regime. Post-reaction, the catalyst is further characterised by powder X-ray diffraction, transmission electron microscopy and Raman scattering. In a comparable fashion to that seen for the ‘dry’ reforming experiments, the catalyst retains substantial quantities of carbon in the form of filamentous coke. The role for hydrogen incorporation by the catalyst is briefly considered.

Loading Intensity Prediction by Velocity and the OMNI-RES 0-10 Scale in Bench Press.

Science.gov (United States)

Naclerio, Fernando; Larumbe-Zabala, Eneko

2017-02-01

Naclerio, F and Larumbe-Zabala, E. Loading intensity prediction by velocity and the OMNI-RES 0-10 scale in bench press. J Strength Cond Res 32(1): 323-329, 2017-This study examined the possibility of using movement velocity and the perceived exertion as indicators of relative load in the bench press (BP) exercise. A total of 308 young, healthy, resistance trained athletes (242 men and 66 women) performed a progressive strength test up to the one repetition maximum for the individual determination of the full load-velocity and load-exertion relationships. Longitudinal regression models were used to predict the relative load from the average velocity (AV) and the OMNI-Resistance Exercise Scales (OMNI-RES 0-10 scale), considering sets as the time-related variable. Load associated with the AV and the OMNI-RES 0-10 scale value expressed after performing a set of 1-3 repetitions were used to construct 2 adjusted predictive equations: Relative load = 107.75 - 62.97 × average velocity; and Relative load = 29.03 + 7.26 × OMNI-RES 0-10 scale value. The 2 models were capable of estimating the relative load with an accuracy of 84 and 93%, respectively. These findings confirm the ability of the 2 calculated regression models, using load-velocity and load-exertion from the OMNI-RES 0-10 scale, to accurately predict strength performance in BP.

Modeling of electrochemistry and steam-methane reforming performance for simulating pressurized solid oxide fuel cell stacks

Energy Technology Data Exchange (ETDEWEB)

Recknagle, Kurtis P.; Ryan, Emily M.; Koeppel, Brian J.; Mahoney, Lenna A.; Khaleel, Moe A. [Pacific Northwest National Laboratory, Richland, WA 99352 (United States)

2010-10-01

This paper examines the electrochemical and direct internal steam-methane reforming performance of the solid oxide fuel cell when subjected to pressurization. Pressurized operation boosts the Nernst potential and decreases the activation polarization, both of which serve to increase cell voltage and power while lowering the heat load and operating temperature. A model considering the activation polarization in both the fuel and the air electrodes was adopted to address this effect on the electrochemical performance. The pressurized methane conversion kinetics and the increase in equilibrium methane concentration are considered in a new rate expression. The models were then applied in simulations to predict how the distributions of direct internal reforming rate, temperature, and current density are effected within stacks operating at elevated pressure. A generic 10 cm counter-flow stack model was created and used for the simulations of pressurized operation. The predictions showed improved thermal and electrical performance with increased operating pressure. The average and maximum cell temperatures decreased by 3% (20 C) while the cell voltage increased by 9% as the operating pressure was increased from 1 to 10 atm. (author)

Hydrogen production from steam reforming of ethanol over Ni/MgO-CeO_2 catalyst at low temperature

Institute of Scientific and Technical Information of China (English)

石秋杰; 刘承伟; 谌伟庆

2009-01-01

MgO,CeO2 and MgO-CeO2 with different mole ratio of Mg:Ce were prepared by solid-phase burning method.Catalysts Ni/MgO,Ni/CeO2 and Ni/MgO-CeO2 were prepared by impregnation method.The catalytic properties were evaluated in ethanol steam reforming(ESR) reaction.Specific surface areas of the supports were measured by nitrogen adsorption-desorption at 77 K,and the catalysts were characterized with X-ray diffraction(XRD),temperature programmed reduction(TPR) and thermogravimetric(TG).The results showed that well...

JV TASK 45-MERCURY CONTROL TECHNOLOGIES FOR ELECTRIC UTILITIES BURNING LIGNITE COAL, PHASE I BENCH-AND PILOT-SCALE TESTING

Energy Technology Data Exchange (ETDEWEB)

John H. Pavlish; Michael J. Holmes; Steven A. Benson; Charlene R. Crocker; Edwin S. Olson; Kevin C. Galbreath; Ye Zhuang; Brandon M. Pavlish

2003-10-01

The Energy & Environmental Research Center has completed the first phase of a 3-year, two-phase consortium project to develop and demonstrate mercury control technologies for utilities that burn lignite coal. The overall project goal is to maintain the viability of lignite-based energy production by providing utilities with low-cost options for meeting future mercury regulations. Phase I objectives are to develop a better understanding of mercury interactions with flue gas constituents, test a range of sorbent-based technologies targeted at removing elemental mercury (Hg{sup o}) from flue gases, and demonstrate the effectiveness of the most promising technologies at the pilot scale. The Phase II objectives are to demonstrate and quantify sorbent technology effectiveness, performance, and cost at a sponsor-owned and operated power plant. Phase I results are presented in this report along with a brief overview of the Phase II plans. Bench-scale testing provided information on mercury interactions with flue gas constituents and relative performances of the various sorbents. Activated carbons were prepared from relatively high-sodium lignites by carbonization at 400 C (752 F), followed by steam activation at 750 C (1382 F) and 800 C (1472 F). Luscar char was also steam-activated at these conditions. These lignite-based activated carbons, along with commercially available DARCO FGD and an oxidized calcium silicate, were tested in a thin-film, fixed-bed, bench-scale reactor using a simulated lignitic flue gas consisting of 10 {micro}g/Nm{sup 3} Hg{sup 0}, 6% O{sub 2}, 12% CO{sub 2}, 15% H{sub 2}O, 580 ppm SO{sub 2}, 120 ppm NO, 6 ppm NO{sub 2}, and 1 ppm HCl in N{sub 2}. All of the lignite-based activated (750 C, 1382 F) carbons required a 30-45-minute conditioning period in the simulated lignite flue gas before they exhibited good mercury sorption capacities. The unactivated Luscar char and oxidized calcium silicate were ineffective in capturing mercury. Lignite

Steam reforming of methanol over oxide decorated nanoporous gold catalysts: a combined in situ FTIR and flow reactor study.

Science.gov (United States)

Shi, J; Mahr, C; Murshed, M M; Gesing, T M; Rosenauer, A; Bäumer, M; Wittstock, A

2017-03-29

Methanol as a green and renewable resource can be used to generate hydrogen by reforming, i.e., its catalytic oxidation with water. In combination with a fuel cell this hydrogen can be converted into electrical energy, a favorable concept, in particular for mobile applications. Its realization requires the development of novel types of structured catalysts, applicable in small scale reactor designs. Here, three different types of such catalysts were investigated for the steam reforming of methanol (SRM). Oxides such as TiO 2 and CeO 2 and mixtures thereof (Ce 1 Ti 2 O x ) were deposited inside a bulk nanoporous gold (npAu) material using wet chemical impregnation procedures. Transmission electron and scanning electron microscopy reveal oxide nanoparticles (1-2 nm in size) abundantly covering the strongly curved surface of the nanoporous gold host (ligaments and pores on the order of 40 nm in size). These catalysts were investigated in a laboratory scaled flow reactor. First conversion of methanol was detected at 200 °C. The measured turn over frequency at 300 °C of the CeO x /npAu catalyst was 0.06 s -1 . Parallel investigation by in situ infrared spectroscopy (DRIFTS) reveals that the activation of water and the formation of OH ads are the key to the activity/selectivity of the catalysts. While all catalysts generate sufficient OH ads to prevent complete dehydrogenation of methanol to CO, only the most active catalysts (e.g., CeO x /npAu) show direct reaction with formic acid and its decomposition to CO 2 and H 2 . The combination of flow reactor studies and in operando DRIFTS, thus, opens the door to further development of this type of catalyst.

CRUCIBLE TESTING OF TANK 48 RADIOACTIVE WASTE SAMPLE USING FBSR TECHNOLOGY FOR ORGANIC DESTRUCTION

International Nuclear Information System (INIS)

Hammond, C; William Pepper, W

2008-01-01

The purpose of crucible scale testing with actual radioactive Tank 48H material was to duplicate the test results that had been previously performed on simulant Tank 48H material. The earlier crucible scale testing using simulants was successful in demonstrating that bench scale crucible tests produce results that are indicative of actual Fluidized Bed Steam Reforming (FBSR) pilot scale tests. Thus, comparison of the results using radioactive Tank 48H feed to those reported earlier with simulants would then provide proof that the radioactive tank waste behaves in a similar manner to the simulant. Demonstration of similar behavior for the actual radioactive Tank 48H slurry to the simulant is important as a preliminary or preparation step for the more complex bench-scale steam reformer unit that is planned for radioactive application in the Savannah River National Laboratory (SRNL) Shielded Cells Facility (SCF) later in 2008. The goals of this crucible-scale testing were to show 99% destruction of tetraphenylborate and to demonstrate that the final solid product produced is sodium carbonate. Testing protocol was repeated using the specifications of earlier simulant crucible scale testing, that is sealed high purity alumina crucibles containing a pre-carbonated and evaporated Tank 48H material. Sealing of the crucibles was accomplished by using an inorganic 'nepheline' sealant. The sealed crucibles were heat-treated at 650 C under constant argon flow to inert the system. Final product REDOX measurements were performed to establish the REDuction/OXidation (REDOX) state of known amounts of added iron species in the final product. These REDOX measurements confirm the processing conditions (pyrolysis occurring at low oxygen fugacity) of the sealed crucible environment which is the environment actually achieved in the fluidized bed steam reformer process. Solid product dissolution in water was used to measure soluble cations and anions, and to investigate insoluble

Hydrogen Production from Cyclic Chemical Looping Steam Methane Reforming over Yttrium Promoted Ni/SBA-16 Oxygen Carrier

Directory of Open Access Journals (Sweden)

Sanaz Daneshmand-Jahromi

2017-09-01

Full Text Available In this work, the modification of Ni/SBA-16 oxygen carrier (OC with yttrium promoter is investigated. The yttrium promoted Ni-based oxygen carrier was synthesized via co-impregnation method and applied in chemical looping steam methane reforming (CL-SMR process, which is used for the production of clean energy carrier. The reaction temperature (500–750 °C, Y loading (2.5–7.4 wt. %, steam/carbon molar ratio (1–5, Ni loading (10–30 wt. % and life time of OCs over 16 cycles at 650 °C were studied to investigate and optimize the structure of OC and process temperature with maximizing average methane conversion and hydrogen production yield. The synthesized OCs were characterized by multiples techniques. The results of X-ray powder diffraction (XRD and energy dispersive X-ray spectroscopy (EDX of reacted OCs showed that the presence of Y particles on the surface of OCs reduces the coke formation. The smaller NiO species were found for the yttrium promoted OC and therefore the distribution of Ni particles was improved. The reduction-oxidation (redox results revealed that 25Ni-2.5Y/SBA-16 OC has the highest catalytic activity of about 99.83% average CH4 conversion and 85.34% H2 production yield at reduction temperature of 650 °C with the steam to carbon molar ratio of 2.

A Phenomenological Study on the Synergistic Role of Precious Metals in the Steam Reforming of Logistic Fuels on Bimetal-Supported Catalysts

Directory of Open Access Journals (Sweden)

Abdul-Majeed Azad

2011-01-01

Full Text Available Fuel processors are required to convert sulfur-laden logistic fuels into hydrogen-rich reformate and deliver to the fuel cell stack with little or no sulfur. Since sulfur poisons and deactivates the reforming catalyst, robust sulfur-tolerant catalysts ought to be developed. In this paper, the development, characterization and evaluation of a series of reforming catalysts containing two noble metals (with total metal loading not exceeding 1 weight percent supported on nanoscale ceria for the steam-reforming of kerosene is reported. Due to inherent synergy, a bimetallic catalyst is superior to its monometallic analog, for the same level of loading. The choice of noble metal combination in the bimetallic formulations plays a vital and meaningful role in their performance. Presence of ruthenium and/or rhodium in formulations containing palladium showed improved sulfur tolerance and significant enhancement in their catalytic activity and stability. Rhodium was responsible for higher hydrogen yields in the logistic fuel reformate. Duration of steady hydrogen production was higher in the case of RhPd (75 h than for RuPd (68 h; hydrogen generation was stable over the longest period (88 h with RuRh containing no Pd. A mechanistic correlation between the characteristic role of precious metals in the presence of each other is discussed.

Advances in catalysts for internal reforming in high temperature fuel cells

Science.gov (United States)

Dicks, A. L.

Catalytic steam reforming of natural gas is an attractive method of producing the hydrogen required by the present generation of fuel cells. The molten carbonate (MCFC) and solid oxide (SOFC) fuel cells operate at high enough temperatures for the endothermic steam reforming reaction to be carried out within the stack. For the MCFC, the conventional anodes have insufficient activity to catalyse the steam reforming of natural gas. For these cells, internal reforming can be achieved only with the addition of a separate catalyst, preferably located in close proximity to the anode. However, in the so-called `Direct Internal Reforming' configuration, attack from alkali in the MCFC may severely limit catalyst lifetime. In the case of the state-of-the-art SOFC, natural gas can be reformed directly on the nickel cermet anode. However, in the SOFC, temperature variations in the cell caused by the reforming reaction may limit the amount of internal reforming that can be allowed in practice. In addition, some external pre-reforming may be desirable to remove high molecular weight hydrocarbons from the fuel gas, which would otherwise crack to produce elemental carbon. Degradation of the SOFC anode may also be a problem when internal reforming is carried out. This has prompted several research groups to investigate the use of alternative anode materials.

Simulating and Optimizing Hydrogen Production by Low-pressure Autothermal Reforming of Natural Gas using Non-dominated Sorting Genetic Algorithm-II

OpenAIRE

Azarhoosh, M. J.; Ale Ebrahim, H.; Pourtarah, S. H.

2016-01-01

Conventional hydrogen production plants consist of natural gas steam reforming to CO+3H2 on Ni catalysts in a furnace, water-gas shift reaction for converting CO into CO2 and CO2 absorption. A new alternative method for highly endothermic steam reforming is autothermal reforming (steam reforming with air input to the reactor) without the need for external heating. In this study, hydrogen production by autothermal reforming for fuel cells (base case) was simulated based on a heterogeneous and ...

Scaling up Education Reform: Addressing the Politics of Disparity

Science.gov (United States)

Bishop, Russell; O'Sullivan, Dominic; Berryman, Mere

2010-01-01

What is school reform? What makes it sustainable? Who needs to be involved? How is scaling up achieved? This book is about the need for educational reforms that have built into them, from the outset, those elements that will see them sustained in the original sites and spread to others. Using the Te Kotahitanga Project as a model the authors…

Accumulation of uranium, cesium, and radium by microbial cells: bench-scale studies

International Nuclear Information System (INIS)

Strandberg, G.W.; Shumate, S.E. II.

1982-07-01

This report describes bench-scale studies on the utilization of microbial cells for the concentration and removal of uranium, radium, and cesium from nuclear processing waste streams. Included are studies aimed at elucidating the basic mechanism of uranium uptake, process development efforts for the use of a combined denitrification-uranium removal process to treat a specific nuclear processing waste stream, and a preliminary investigation of the applicability of microorganisms for the removal of 137 Cs and 226 Ra from existing waste solutions

Reforming technology for syngas production

International Nuclear Information System (INIS)

Epstein, M.

1997-01-01

Methane forming reactions using either steam or CO 2 have been known to industry for a long time. These endothermic reactions require the investment of a relatively large amount of energy. German researchers, in the 1970's, conceived and developed the idea to use this reaction and the reverse methanation reaction in a closed loop for the transportation and distribution of nuclear heat. The idea was also adopted for use with solar energy as a heat source. Utilizing solar energy as the heat source, the Weismann Institute of Science has fabricated, installed and operated a complete loop capable of the conversion and transportation of over 400 kW of heat. This system can be operated with a wide range of CO 2 /H 2 O/CH 4 feed mixtures. Steam reforming is the common reforming reaction in the ''open loop'' mode for the purpose of synthesis gas production. This is accomplished with a large excess of steam on a nickel catalyst. However, it has only recently been recognized that there is also a substantial market for CO 2 reforming. The CO 2 /CH 4 mixture in various proportions exists in many places and has, so far, not been used efficiently. The sources for this mixture are biogas produced in anaerobic digestion processes and gas resources such as the NATUNA gas field in Indonesia, and many others. Therefore, the system of CO 2 /CH 4 deserves more attention. Commercial catalysts used for steam reforming based on nickel are not suitable for this system. Therefore, other catalysts based on Rhodium and Ruthenium have been developed and some performance data is presented in this paper. Also presented is a conceptual schematic layout of a CO 2 reforming plant and matching methanator. A computer code for a detailed design of the entire loop in a commercial size system has been prepared where optimized operational conditions as well as equipment parameters can be determined. (author). 3 figs, 3 tabs

Scaled physical model studies of the steam drive process. First annual report, September 1977-September 1978

Energy Technology Data Exchange (ETDEWEB)

Doscher, T M

1980-12-01

Scaling laws of the heat transport mechanism in steam displacement processes are developed based upon an integral energy balance equation. Unlike the differential approach adopted by previous workers, the above scaling laws do not necessitate the use of any empirical correction factor as has been done in previous scaling calculations. The results provide a complete and consistent scale-down of the energy transport behavior, which is the critical mechanism for the success of a steam injection process. In the course of the study, the scaling problems associated with relative permeability and capillary pressure are also discussed. A method which has often been used in scaling nonthermal displacement processes is applied to reduce errors due to scaling in relative permeability. Both dimensional and inspectional analyses are applied to illustrate their use in steam processes. Scale-up laws appeared in the literature and those used in this study are compared and numerical examples are given.

Effect study of the support in nickel and cobalt catalysts for obtaining hydrogen from ethanol steam reforming

International Nuclear Information System (INIS)

Silva, Sirlane Gomes da

2013-01-01

A range of oxide-supported metal catalysts have been investigated for the steam reforming of ethanol for the production of hydrogen and subsequent application in fuel cells. The catalysts were synthesized by the co-precipitation and internal gelification methods using cobalt and nickel as active metals supported on aluminum, zirconium, lanthanum and cerium oxides. After prepared and calcined at 550 Cº the solids were fully characterized by different techniques such as X-rays diffraction(DRX), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy, nitrogen adsorption (B.E.T), temperature-programmed reduction in H2 (TPR-H2) and thermogravimetric analysis. The catalytic tests were performed in a monolithic quartz reactor and submitted to different thermodynamic conditions of steam reforming of ethanol at temperatures varying from 500º C to 800 ºC. The product gas streams from the reactor were analyzed by an on-line gas chromatograph. The cobalt/nickel catalyst supported on a ceria-lanthania mixture (Co 10% / Ni 5% - CeO 2 La 2 O 3 ) showed good catalytic performance in hydrogen selectivity reaching a concentration greater than 65%, when compared to other catalytic systems such as: Co 10% / Ni5% - CeO 2 ; Co 10% / Ni 5% - CeO 2 ZrO 2 ; Co 10% / Ni 5% - ZrO 2 ; Co 10% / Ni 5% - La 2 O 3 ; Co 10% / Ni 5% - CeO 2 La 2 O 3 /K 2% ; Co 10 % / Ni 5% - CeO 2 La 2 O 3 / Na 2% ; Ni 10% / Co 5% - CeO 2 La 2 O 3 ; Co-Al 2 O 3 e Co-Al 2 O 3 CeO 2 . (author)

Circulating fluidized bed reformer-regenerator system for hydrogen production from methane. Paper no. IGEC-1-092

International Nuclear Information System (INIS)

Prasad, P.; Elnashaie, S.S.E.H.

2005-01-01

Steam reforming is presently the principal route for large-scale hydrogen production from natural gas. This paper proposes a novel concept of a reactor-regenerator type circulating fluidized bed (Prasad and Elnashaie, 2002) for efficient production of hydrogen. Carbon is optimally allowed to form on the catalyst in the reactor section through methane cracking and Boudouard coking reactions, and the deactivated catalyst is regenerated in the regenerator by burning off the carbon. This concept of carbon formation and burning cannot be used in a fixed bed configuration but is possible in the proposed novel Circulating Fluidized Bed (CFB) configuration, which employs a reactor-regenerator type of configuration. Allowing both carbon formation and steam reforming to occur simultaneously by introducing steam as part of the feed, gives more than 3 moles hydrogen per mole of methane at almost zero energy consumption. The steam can be fed as water at room temperature, and the hot catalyst returning from the regenerator can be used to vaporize it into steam. This route is the most efficient from both hydrogen yield and energy consumption points of view. This CFB configuration exhibits the bifurcation behavior and the present paper reports an investigation of its static bifurcation characteristics through a rigorous mathematical model. (author)

Evaluation of Large-scale Public Sector Reforms

DEFF Research Database (Denmark)

Breidahl, Karen Nielsen; Gjelstrup, Gunnar; Hansen, Hanne Foss

2017-01-01

and more delimited policy areas take place. In our analysis we apply four governance perspectives (rational-instrumental, rational-interest based, institutional-cultural and a chaos perspective) in a comparative analysis of the evaluations of two large-scale public sector reforms in Denmark and Norway. We...

Bench-Scale and Pilot-Scale Treatment Technologies for the ...

Science.gov (United States)

Coal mine water (CMW) is typically treated to remove suspended solids, acidity, and soluble metals, but high concentrations of total dissolved solids (TDS) have been reported to impact the environment at several CMW discharge points. Consequently, various states have established TDS wastewater regulations and the US EPA has proposed a benchmark conductivity limit to reduce TDS impacts in streams near mining sites. Traditional CMW treatment effectively removes some TDS components, but is not effective in removing major salt ions due to their higher solubility. This paper describes the basic principles, effectiveness, advantages and disadvantages of various TDS removal technologies (adsorption, bioremediation, capacitive deionization, desalination, electro-chemical ion exchange, electrocoagulation, electrodialysis, ion exchange, membrane filtration, precipitation, and reverse osmosis) that have at least been tested in bench- and pilot-scale experiments. Recent discussions about new regulations to include total dissolved solids TDS) limits would propel interest in the TDS removal technologies focused on coal mine water. TDS removal is not a new concept and has been developed using different technologies for a number of applications, but coal mine water has unique characteristics (depending on the site, mining process, and solid-water-oxygen interactions), which make it unlikely to have a single technology predominating over others. What are some novel technolog

Heat and fuel coupled operation of a high temperature polymer electrolyte fuel cell with a heat exchanger methanol steam reformer

Science.gov (United States)

Schuller, G.; Vázquez, F. Vidal; Waiblinger, W.; Auvinen, S.; Ribeirinha, P.

2017-04-01

In this work a methanol steam reforming (MSR) reactor has been operated thermally coupled to a high temperature polymer electrolyte fuel cell stack (HT-PEMFC) utilizing its waste heat. The operating temperature of the coupled system was 180 °C which is significantly lower than the conventional operating temperature of the MSR process which is around 250 °C. A newly designed heat exchanger reformer has been developed by VTT (Technical Research Center of Finland LTD) and was equipped with commercially available CuO/ZnO/Al2O3 (BASF RP-60) catalyst. The liquid cooled, 165 cm2, 12-cell stack used for the measurements was supplied by Serenergy A/S. The off-heat from the electrochemical fuel cell reaction was transferred to the reforming reactor using triethylene glycol (TEG) as heat transfer fluid. The system was operated up to 0.4 A cm-2 generating an electrical power output of 427 Wel. A total stack waste heat utilization of 86.4% was achieved. It has been shown that it is possible to transfer sufficient heat from the fuel cell stack to the liquid circuit in order to provide the needed amount for vaporizing and reforming of the methanol-water-mixture. Furthermore a set of recommendations is given for future system design considerations.

Projected hydrogen cost from methane reforming for North America 2015-2050

International Nuclear Information System (INIS)

Vanderveen, K.; Lutz, A.; Klebanoff, L.; Drennen, T.; Keller, J.; Drennen, T.; Kamery, W.

2006-01-01

The Hydrogen Futures Simulation Model (H 2 Sim) was used to project the cost for hydrogen at the point of sale to light duty vehicles for distributed, small-scale steam methane reforming. Projections cover the period from 2010-2050 in North America, and take into account assumptions about the quantity of recoverable natural gas remaining in North America. We conclude that there is a window for distributed reforming to play a positive role in supplying a H 2 fuel infrastructure, but this window is closing rapidly. The analysis assumes that production from natural gas reserves in North America will peak sometime before 2050 and demand will cause the price to rise after the peak of production in a manner consistent with Hotelling's model. We consider three scenarios for when the peak occurs, and evaluate the impact on the cost of hydrogen fuel produced via distributed small scale reforming in these three scenarios. (authors)

Mechanistic Insights into Catalytic Ethanol Steam Reforming Using Isotope-Labeled Reactants.

Science.gov (United States)

Crowley, Stephen; Castaldi, Marco J

2016-08-26

The low-temperature ethanol steam reforming (ESR) reaction mechanism over a supported Rh/Pt catalyst has been investigated using isotope-labeled EtOH and H2 O. Through strategic isotope labeling, all nonhydrogen atoms were distinct from one another, and allowed an unprecedented level of understanding of the dominant reaction pathways. All combinations of isotope- and non-isotope-labeled atoms were detected in the products, thus there are multiple pathways involved in H2 , CO, CO2 , CH4 , C2 H4 , and C2 H6 product formation. Both the recombination of C species on the surface of the catalyst and preservation of the C-C bond within ethanol are responsible for C2 product formation. Ethylene is not detected until conversion drops below 100 % at t=1.25 h. Also, quantitatively, 57 % of the observed ethylene is formed directly through ethanol dehydration. Finally there is clear evidence to show that oxygen in the SiO2 -ZrO2 support constitutes 10 % of the CO formed during the reaction. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

A comparison of large-scale electron beam and bench-scale 60Co irradiations of simulated aqueous waste streams

Science.gov (United States)

Kurucz, Charles N.; Waite, Thomas D.; Otaño, Suzana E.; Cooper, William J.; Nickelsen, Michael G.

2002-11-01

The effectiveness of using high energy electron beam irradiation for the removal of toxic organic chemicals from water and wastewater has been demonstrated by commercial-scale experiments conducted at the Electron Beam Research Facility (EBRF) located in Miami, Florida and elsewhere. The EBRF treats various waste and water streams up to 450 l min -1 (120 gal min -1) with doses up to 8 kilogray (kGy). Many experiments have been conducted by injecting toxic organic compounds into various plant feed streams and measuring the concentrations of compound(s) before and after exposure to the electron beam at various doses. Extensive experimentation has also been performed by dissolving selected chemicals in 22,700 l (6000 gal) tank trucks of potable water to simulate contaminated groundwater, and pumping the resulting solutions through the electron beam. These large-scale experiments, although necessary to demonstrate the commercial viability of the process, require a great deal of time and effort. This paper compares the results of large-scale electron beam irradiations to those obtained from bench-scale irradiations using gamma rays generated by a 60Co source. Dose constants from exponential contaminant removal models are found to depend on the source of radiation and initial contaminant concentration. Possible reasons for observed differences such as a dose rate effect are discussed. Models for estimating electron beam dose constants from bench-scale gamma experiments are presented. Data used to compare the removal of organic compounds using gamma irradiation and electron beam irradiation are taken from the literature and a series of experiments designed to examine the effects of pH, the presence of turbidity, and initial concentration on the removal of various organic compounds (benzene, toluene, phenol, PCE, TCE and chloroform) from simulated groundwater.

A comparison of large-scale electron beam and bench-scale 60Co irradiations of simulated aqueous waste streams

International Nuclear Information System (INIS)

Kurucz, Charles N.; Waite, Thomas D.; Otano, Suzana E.; Cooper, William J.; Nickelsen, Michael G.

2002-01-01

The effectiveness of using high energy electron beam irradiation for the removal of toxic organic chemicals from water and wastewater has been demonstrated by commercial-scale experiments conducted at the Electron Beam Research Facility (EBRF) located in Miami, Florida and elsewhere. The EBRF treats various waste and water streams up to 450 l min -1 (120 gal min -1 ) with doses up to 8 kilogray (kGy). Many experiments have been conducted by injecting toxic organic compounds into various plant feed streams and measuring the concentrations of compound(s) before and after exposure to the electron beam at various doses. Extensive experimentation has also been performed by dissolving selected chemicals in 22,700 l (6000 gal) tank trucks of potable water to simulate contaminated groundwater, and pumping the resulting solutions through the electron beam. These large-scale experiments, although necessary to demonstrate the commercial viability of the process, require a great deal of time and effort. This paper compares the results of large-scale electron beam irradiations to those obtained from bench-scale irradiations using gamma rays generated by a 60 Co source. Dose constants from exponential contaminant removal models are found to depend on the source of radiation and initial contaminant concentration. Possible reasons for observed differences such as a dose rate effect are discussed. Models for estimating electron beam dose constants from bench-scale gamma experiments are presented. Data used to compare the removal of organic compounds using gamma irradiation and electron beam irradiation are taken from the literature and a series of experiments designed to examine the effects of pH, the presence of turbidity, and initial concentration on the removal of various organic compounds (benzene, toluene, phenol, PCE, TCE and chloroform) from simulated groundwater

Purifier-integrated methanol reformer for fuel cell vehicles

Science.gov (United States)

Han, Jaesung; Kim, Il-soo; Choi, Keun-Sup

We developed a compact, 3-kW, purifier-integrated modular reformer which becomes the building block of full-scale 30-kW or 50-kW methanol fuel processors for fuel cell vehicles. Our proprietary technologies regarding hydrogen purification by composite metal membrane and catalytic combustion by washcoated wire-mesh catalyst were combined with the conventional methanol steam-reforming technology, resulting in higher conversion, excellent quality of product hydrogen, and better thermal efficiency than any other systems using preferential oxidation. In this system, steam reforming, hydrogen purification, and catalytic combustion all take place in a single reactor so that the whole system is compact and easy to operate. Hydrogen from the module is ultrahigh pure (99.9999% or better), hence there is no power degradation of PEMFC stack due to contamination by CO. Also, since only pure hydrogen is supplied to the anode of the PEMFC stack, 100% hydrogen utilization is possible in the stack. The module produces 2.3 Nm 3/h of hydrogen, which is equivalent to 3 kW when PEMFC has 43% efficiency. Thermal efficiency (HHV of product H 2/HHV of MeOH in) of the module is 89% and the power density of the module is 0.77 kW/l. This work was conducted in cooperation with Hyundai Motor Company in the form of a Korean national project. Currently the module is under test with an actual fuel cell stack in order to verify its performance. Sooner or later a full-scale 30-kW system will be constructed by connecting these modules in series and parallel and will serve as the fuel processor for the Korean first fuel cell hybrid vehicle.

Methanol Steam Reforming Promoted by Molten Salt-Modified Platinum on Alumina Catalysts

Science.gov (United States)

Kusche, Matthias; Agel, Friederike; Ní Bhriain, Nollaig; Kaftan, Andre; Laurin, Mathias; Libuda, Jörg; Wasserscheid, Peter

2014-01-01

We herein describe a straight forward procedure to increase the performance of platinum-on-alumina catalysts in methanol steam reforming by applying an alkali hydroxide coating according to the “solid catalyst with ionic liquid layer” (SCILL) approach. We demonstrate by diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and temperature-programmed desorption (TPD) studies that potassium doping plays an important role in the catalyst activation. Moreover, the hygroscopic nature and the basicity of the salt modification contribute to the considerable enhancement in catalytic performance. During reaction, a partly liquid film of alkali hydroxides/carbonates forms on the catalyst/alumina surface, thus significantly enhancing the availability of water at the catalytically active sites. Too high catalyst pore fillings with salt introduce a considerable mass transfer barrier into the system as indicated by kinetic studies. Thus, the optimum interplay between beneficial catalyst modification and detrimental mass transfer effects had to be identified and was found on the applied platinum-on-alumina catalyst at KOH loadings around 7.5 mass %. PMID:25124120

Annual report on experimental operation of mock-up model test facility with a full-scale reaction tube for HTTR hydrogen production system in 2001 fiscal year (Contract research)

International Nuclear Information System (INIS)

Hayashi, Koji; Inagaki, Yoshiyuki; Kato, Michio; Fujisaki, Katsuo; Aita, Hideki; Takeda, Tetsuaki; Nishihara, Tetsuo; Inaba, Yoshitomo; Ohashi, Hirofumi; Katanishi, Shoji; Takada, Shoji; Shimizu, Akira; Morisaki, Norihiro; Sakaki, Akihiro; Maeda, Yukimasa; Sato, Hiroyuki

2005-06-01

This is an annual report on the experimental operation of the mock-up test facility with a full-scale reaction tube for the HTTR hydrogen production system in 2001 fiscal year. The first experimental operation was performed during two weeks from March 1, 2002 to March 13, 2002 to test on the thermal hydraulic performance of the steam reformer and also to train the operators. The thermal hydraulic performance test of the steam reformer was performed to evaluate the heat transfer characteristics between helium gas and process gas in the steam reformer. This report is summarized with an overview of the test, the results and its operation records. (author)

Direct internal steam reforming of ethanol in a solid oxide fuel cell (SOFC) - A thermodynamic analysis

International Nuclear Information System (INIS)

Lima da Silva, Aline; De Fraga Malfatti, Celia; Heck, Nestor Cesar; Melo Halmenschlager, Cibele

2003-01-01

Among the various types of fuel cells, the solid oxide fuel cell (SOFC) has attracted considerable interest due to the possibility for operation with an internal reformer and higher system efficiency. In SOFC, high operative temperature allows the direct conversion of ethanol into H 2 and CO to take place in the electrochemical cell. Ethanol is considered to be an attractive fuel because it is a renewable energy source and presents some advantages over other green fuels such as safety in storage and handling. Direct internal reforming of ethanol, however, can produce undesirable products that diminish system efficiency and, in the case of carbon deposition over the anode, promote the growth of carbon filaments attached to the anode crystallites which generate massive forces within the electrode structure leading to its rapid breakdown. In this context, a thermodynamic analysis is fundamental to predict the product distribution as well as the conditions favorable for carbon to precipitate inside the cell. Despite of such importance, there are few works in literature dealing with thermodynamic analysis of the direct internal steam reforming of ethanol in fuel cell systems. Hence, the aim of this work is to find appropriate ranges for operating conditions where carbon deposition in SOFC with direct internal reforming operation is not feasible, in temperature range of 500- 1200K. The calculation here is more complicated than that for a reformer because the disappearance of hydrogen and the generation of H 2 O from electrochemical reaction must be taken into account. In the present study, the effects of hydrogen consumption on anode components and on carbon formation are investigated. Equilibrium determinations are performed by the Gibbs energy minimization method, considering the following species: H 2 , H 2 O, CH 4 , CO, CO 2 and C gr . (graphite). The effect of the type of solid electrolyte (oxygen-conducting and hydrogen-conducting) on carbon formation is also

Hydrogen Production by Ethanol Steam Reforming (ESR over CeO2 Supported Transition Metal (Fe, Co, Ni, Cu Catalysts: Insight into the Structure-Activity Relationship

Directory of Open Access Journals (Sweden)

Michalis Konsolakis

2016-03-01

Full Text Available The aim of the present work was to investigate steam reforming of ethanol with regard to H2 production over transition metal catalysts supported on CeO2. Various parameters concerning the effect of temperature (400–800 °C, steam-to-carbon (S/C feed ratio (0.5, 1.5, 3, 6, metal entity (Fe, Co, Ni, Cu and metal loading (15–30 wt.% on the catalytic performance, were thoroughly studied. The optimal performance was obtained for the 20 wt.% Co/CeO2 catalyst, achieving a H2 yield of up to 66% at 400 °C. In addition, the Co/CeO2 catalyst demonstrated excellent stability performance in the whole examined temperature range of 400–800 °C. In contrast, a notable stability degradation, especially at low temperatures, was observed for Ni-, Cu-, and Fe-based catalysts, ascribed mainly to carbon deposition. An extensive characterization study, involving N2 adsorption-desorption (BET, X-ray diffraction (XRD, Scanning Electron Microscopy (SEM/EDS, X-ray Photoelectron Spectroscopy (XPS, and Temperature Programmed Reduction (H2-TPR was undertaken to gain insight into the structure-activity correlation. The excellent reforming performance of Co/CeO2 catalysts could be attributed to their intrinsic reactivity towards ethanol reforming in combination to their high surface oxygen concentration, which hinders the deposition of carbonaceous species.

Preparation and characterization of {alpha}-AI{sub 2}O{sub 3} catalytic supports. Application to methane steam reforming; Preparation et caracterisation de supports catalytiques d`Al{sub 2}O{sub 3} {alpha}. Application au vaporeformange du methane

Energy Technology Data Exchange (ETDEWEB)

Marturano, M.A.; Ferretti, O.A. [Centro de Investigacion y Desarrollo en Procesos Cataliticas (CINDECA), La Plata (Argentina); Aglietti, E.F. [Centro de Tecnologia de Recursos Minerales y Ceramica (CETMIC, UNPL and CONICET), (Argentina)

1995-12-31

{alpha}Al{sub 2}O{sub 3} preformed bodies are widely used as catalytic supports in many industrial processes as for instance steam reforming. In this work, is particularly studied the textural, structural, morphological and mechanical properties of {alpha}-Al{sub 2}O{sub 3} supports as a function of the characteristics of the starting alumina and of the bonding agents used. The performance of these supports in the final catalyst in methane steam reforming is also studies. It was found that textural and morphological properties are determined only by the starting alumina utilized in support preparation. When non-stabilized alumina powders are used (small grains), mechanical properties of the support are controlled by the sintering process, independently of the binder used. When stabilized alumina powders are used (large grains) the existence of ceramic and chemical bonds leads to better results (bentonite and mono-aluminium phosphate, BM supports). Materials with adequate catalytic properties in methane steam reforming can be obtained when using supports prepared from powders easily found (commercial raw alumina) 20 refs.

Methane Steam Reforming over an Ni-YSZ Solid Oxide Fuel Cell Anode in Stack Configuration

Directory of Open Access Journals (Sweden)

D. Mogensen

2014-01-01

Full Text Available The kinetics of catalytic steam reforming of methane over an Ni-YSZ anode of a solid oxide fuel cell (SOFC have been investigated with the cell placed in a stack configuration. In order to decrease the degree of conversion, a single cell stack with reduced area was used. Measurements were performed in the temperature range 600–800°C and the partial pressures of all reactants and products were varied. The obtained rates could be well fitted with a power law expression (r ∝PCH40.7. A simple model is presented which is capable of predicting the methane conversion in a stack configuration from intrinsic kinetics of the anode support material. The predictions are compared with the stack measurements presented here, and good agreement is observed.

Evaluation of Large-Scale Public-Sector Reforms: A Comparative Analysis

Science.gov (United States)

Breidahl, Karen N.; Gjelstrup, Gunnar; Hansen, Hanne Foss; Hansen, Morten Balle

2017-01-01

Research on the evaluation of large-scale public-sector reforms is rare. This article sets out to fill that gap in the evaluation literature and argues that it is of vital importance since the impact of such reforms is considerable and they change the context in which evaluations of other and more delimited policy areas take place. In our…

Interferometric 30 m bench for calibrations of 1D scales and optical distance measuring instruments

International Nuclear Information System (INIS)

Unkuri, J; Rantanen, A; Manninen, J; Esala, V-P; Lassila, A

2012-01-01

During construction of a new metrology building for MIKES, a 30 m interferometric bench was designed. The objective was to implement a straight, stable, adjustable and multifunctional 30 m measuring bench for calibrations. Special attention was paid to eliminating the effects of thermal expansion and inevitable concrete shrinkage. The linear guide, situated on top of a monolithic concrete beam, comprises two parallel round shafts with adjustable fixtures every 1 m. A carriage is moved along the rail and its position is followed by a reference interferometer. Depending on the measurement task, one or two retro-reflectors are fixed on the carriage. A microscope with a CCD camera and a monitor can be used to detect line mark positions on different line standards. When calibrating optical distance measuring instruments, various targets can be fixed to the carriage. For the most accurate measurements an online Abbe-error correction based on simultaneous carriage pitch measurement by a separate laser interferometer is applied. The bench is used for calibrations of machinist scales, tapes, circometers, electronic distance meters, total stations and laser trackers. The estimated expanded uncertainty for 30 m displacement for highest accuracy calibrations is 2.6 µm. (paper)

Investigation of a methanol reformer concept considering the particular impact of dynamics and long-term stability for use in a fuel-cell-powered passenger car

Science.gov (United States)

Peters, R.; Düsterwald, H. G.; Höhlein, B.

A methanol reformer concept including a reformer, a catalytic burner, a gas cleaning unit, a PEMFC and an electric motor for use in fuel-cell-powered passenger cars was investigated. Special emphasis was placed on the dynamics and the long-term stability of the reformer. Experiments on a laboratory scale were performed in a methanol steam reformer consisting of four different reactor tubes, which were separately balanced. Due to the endothermy of the steam reforming reaction of methanol, a sharp drop in the reaction temperature of about 50 K occurs at the beginning of the catalyst bed. This agrees well with the high catalytic activity at the entrance of the catalyst bed. Forty-five percent of the methanol was converted within the first 10 cm of the catalyst bed where 12.6 g of the CuO/ZnO catalyst was located. Furthermore, CO formation during methanol steam reforming strongly depends on methanol conversion. Long-term measurements for more than 700 h show that the active reaction zone moved through the catalyst bed. Calculations, on the basis of these experiments, revealed that 63 g of reforming catalyst was necessary for mobile PEMFC applications, in this case for 400 W el at a system efficiency of 42% and a theoretical specific hydrogen production of 5.2 m 3n/(h kg Cat). This amount of catalyst was assumed to maintain a hydrogen production of at least 80% of the original amount over an operating range of 3864 h. Cycled start-up and shut-down processes of the methanol steam reformer under nitrogen and hydrogen atmospheres did not harm the catalytic activity. The simulation of the breakdown of the heating system, in which a liquid water/methanol mixture was in close contact with the catalyst, did not reveal any deactivation of the catalytic activity.

Hydrogen production from raw bioethanol steam reforming: optimization of catalyst composition with improved stability against various impurities

International Nuclear Information System (INIS)

Le Valant, A.; Can, F.; Bion, N.; Epron, F.; Duprez, D.

2009-01-01

Usually, ethanol steam reforming is performed using pure ethanol, whereas the use of raw bioethanol is of major importance for a cost effective industrial application. Raw bioethanol contains higher alcohols as the main impurities and also aldehydes, amines, acids and esters. The effect of these impurities on the catalytic performances for ethanol steam reforming (ESR) has been studied, using a reference catalyst, Rh/MgAl 2 O 4 . It was shown that the aldehyde, the amine and methanol has no negative effect on the catalytic performances, contrary to the ester, acid and higher alcohols. The deactivation is mainly explained by coke formation favored by the presence of these impurities in the feed. In order to improve the stability of the catalyst and its performances in the presence of these deactivating impurities, the catalyst formulation, i.e. the composition of the support and of the metallic phase, was modified. The addition of rare earth elements instead of magnesium to the alumina support leads to a decrease of the strong and medium acid sites and to an increase of the basicity. On these modified supports, the dehydration reaction, leading to olefins, which are coke precursors, is disfavored, the ethanol conversion and the hydrogen yield are increased. The best catalytic performances were obtained with Rh/Y-Al 2 O 3 . Then, the metallic phase was also modified by adding a second metal (Ni, Pt or Pd). The Rh-Ni/Y-Al 2 O 3 catalyst leads to the highest hydrogen yield. This catalyst, tested in the presence of raw bioethanol during 24h was very stable compared to the reference catalyst Rh/MgAl 2 O 4 , which was strongly deactivated after 2h of time-on-stream. (author)

Pembuatan Katalis Cu/ZnO/Al2O3 untuk Proses Steam Reforming Metanol menjadi Hidrogen sebagai Bahan Bakar Alternatif

Directory of Open Access Journals (Sweden)

Husni Husin

2010-06-01

Full Text Available Study on the use of copper zinc oxide supported on alumina catalyst for steam reforming of methanol to hydrogen has been done. The aim of this work is to study the catalytic properties of copper based catalysts used in the steam reforming of methanol. This method is known as one of the most favorable catalytic processes for producing hydrogen on-board. The catalyst was prepared by impregnation method with Cu loading of 5%, 10%, and 15%,. The X-ray diffraction pattern shows that the catalyst compositions are Cu, CuO, ZnO, and Al2O3. The reactions were carried out in the fixed bed tubular reactor operating at temperatures of 150oC, 200oC, 250oC, 300oC, and 350oC and atmospheric pressure. The product was analyzed using Shimadzu Gas Chromatography GC 8A with mole sieve 5A and porapak-N column 80/100 mesh. The performance of the catalyst shows that the highest methanol conversion was 86% over Cu/ZnO/Al2O3 catalyst with 15% of Cu loading. The selectivity and yield of hydrogen was 66% and 57% respectively over Cu/ZnO/Al2O3 catalyst with 15% of Cu loading. Selectivity of carbon dioxide is 18% over Cu/ZnO/Al2O3 catalyst with 15% of Cu loading at 300oC. Keywords: alumina oxide catalyst, copper zinc oxide, hydrogen, impregnation

Effect of Ce and Zr Addition to Ni/SiO2 Catalysts for Hydrogen Production through Ethanol Steam Reforming

Directory of Open Access Journals (Sweden)

Jose Antonio Calles

2015-01-01

Full Text Available A series of Ni/Ce\\(_{x}\\Zr\\(_{1-x}\\O\\(_{2}\\/SiO\\(_{2}\\ catalysts with different Zr/Ce mass ratios were prepared by incipient wetness impregnation. Ni/SiO\\(_{2}\\, Ni/CeO\\(_{2}\\ and Ni/ZrO\\(_{2}\\ were also prepared as reference materials to compare. Catalysts' performances were tested in ethanol steam reforming for hydrogen production and characterized by XRD, H\\(_{2}\\-temperature programmed reduction (TPR, NH\\(_{3}\\-temperature programmed desorption (TPD, TEM, ICP-AES and N\\(_{2}\\-sorption measurements. The Ni/SiO\\(_{2}\\ catalyst led to a higher hydrogen selectivity than Ni/CeO\\(_{2}\\ and Ni/ZrO\\(_{2}\\, but it could not maintain complete ethanol conversion due to deactivation. The incorporation of Ce or Zr prior to Ni on the silica support resulted in catalysts with better performance for steam reforming, keeping complete ethanol conversion over time. When both Zr and Ce were incorporated into the catalyst, Ce\\(_{x}\\Zr\\(_{1-x}\\O\\(_{2}\\ solid solution was formed, as confirmed by XRD analyses. TPR results revealed stronger Ni-support interaction in the Ce\\(_{x}\\Zr\\(_{1-x}\\O\\(_{2}\\-modified catalysts than in Ni/SiO\\(_{2}\\ one, which can be attributed to an increase of the dispersion of Ni species. All of the Ni/Ce\\(_{x}\\Zr\\(_{1-x}\\O\\(_{2}\\/SiO\\(_{2}\\ catalysts exhibited good catalytic activity and stability after 8 h of time on stream at 600°. The best catalytic performance in terms of hydrogen selectivity was achieved when the Zr/Ce mass ratio was three.

Runoff and sediment generation on bench -terraced hillsides: measurements and up-scaling of a field-based model

NARCIS (Netherlands)

van Dijk, A.I.J.M.; Bruijnzeel, L.A.; Vertessy, R.A.; Ruijter, J.

2006-01-01

Despite widespread bench-terracing, stream sediment yields from agricultural hillsides in upland West Java remain high. We studied the causes of this lack of effect by combining measurements at different spatial scales using an erosion process model. Event runoff and sediment yield from two 4-ha

Characterization and Modeling of a Methanol Reforming Fuel Cell System

DEFF Research Database (Denmark)

Sahlin, Simon Lennart

topologies is the Reformed Methanol Fuel Cell (RMFC) system that operates on a mix of methanol and water. The fuel is reformed with a steam reforming to a hydrogen rich gas, however with additional formation of Carbon Monoxide and Carbon Dioxide. High Temperature Polymer Electrolyte Membrane Fuel Cell (HT...... to heat up the steam reforming process. However, utilizing the excess hydrogen in the system complicates the RMFC system as the amount of hydrogen can vary depending on the fuel methanol supply, fuel cell load and the reformer gas composition. This PhD study has therefore been involved in investigating......Many fuel cells systems today are operated with compressed hydrogen which has great benefits because of the purity of the hydrogen and the relatively simple storage of the fuel. However, compressed hydrogen is stored in the range of 800 bar, which can be expensive to compress.One of the interesting...

Thermodynamic analysis of ethanol reforming for hydrogen production

International Nuclear Information System (INIS)

Sun, Shaohui; Yan, Wei; Sun, Peiqin; Chen, Junwu

2012-01-01

This work presents the simulated equilibrium compositions of ethanol steam reforming (SR), partial oxidation (POX) and auto-thermal reforming (ATR) at a large temperature range, steam-to-ethanol and oxygen-to-ethanol molar ratios. The simulation work shows that the moles of hydrogen yield per mole ethanol are of this order: SR > ATR > POX. The results are compared with other simulation works and fitted models, which show that all the simulation results obtained with different methods agree well with each other. And the fitted models are in highly consistency with very small deviations. Moreover, the thermal-neutral point in corresponding to temperature, steam-to-ethanol and oxygen-to-ethanol mole ratios of ethanol ATR is estimated. The result shows that with the increasing of oxygen-to-ethanol mole ratio, the T-N point moves to higher temperatures; with the increasing of steam-to-ethanol mole ratio, the T-N point moves to lower temperatures. Furthermore, the energy exchanges of the reforming process and the whole process and the thermal efficiencies are also analyzed in the present work and that the energy demands and generated in the whole process are greater than the reforming process can be obtained. Finally, the optimum reaction conditions are selected. -- Highlights: ► The equilibrium compositions simulated by different researchers with different methods are compared. ► The simulation results are fitted with polynomials for convenient reference. ► The energy balance and thermal efficiencies are analyzed. ► The optimum reaction conditions of ethanol POX, SR and ATR for hydrogen production are selected.

Compact methanol reformer test for fuel-cell powered light-duty vehicles

Energy Technology Data Exchange (ETDEWEB)

Emonts, B; Hoehlein, B; Peters, R [Forschungszentrum Juelich GmbH (Germany). Inst. fuer Energieverfahrenstechnik (IEV); Hansen, J B; Joergensen, S L [Haldor Topsoe A/S, Lyngby (Denmark)

1998-03-15

On-board production of hydrogen from methanol based on a steam reformer in connection with the use of low-temperature fuel-cells (PEMFC) is an attractive option as energy conversion unit for light-duty vehicles. A steam reforming process at higher pressures with an external burner offers advantages in comparison to a steam reformer with integrated partial oxidation in terms of total efficiency for electricity production. The main aim of a common project carried out by the Forschungszentrum Juelich (FZJ), Haldor Topsoee A/S (HTAS) and Siemens AG is to design, to construct and to test a steam reformer reactor concept (HTAS) with external catalytic burner (FZJ) as heat source as well as catalysts for heterogeneously catalyzed hydrogen production (HTAS), concepts for gas treatment (HTAS, FZJ) and a low-temperature fuel cell (Siemens). Based on the experimental results obtained so far concerning methanol reformers, catalytic burners and gas conditioning units, our report describes the total system, a test unit and preliminary test results related to a hydrogen production capacity of 50 kW (LHV) and dynamic operating conditions. This hydrogen production system is aimed at reducing the specific weight (<2 kg/kW{sub th} or 4 kg/kW{sub el}) combined with high efficiency for net electricity generation from methanol (about 50%) and low specific emissions. The application of Pd-membranes as gas cleaning unit fulfill the requirements with high hydrogen permeability and low cost of the noble metal. (orig.)

Thermodynamic comparison of two processes of hydrogen production: steam methane reforming-A solar thermochemical process

International Nuclear Information System (INIS)

Gomri, Rabah; Boumaza, Mourad

2006-01-01

Hydrogen is mainly employed like primary product, for the synthesis of ammonia. The ammonia is synthesized by chemically combining hydrogen and nitrogen under pressure, in the presence of a catalyst. This ammonia is used, for the production of the nitrate fertilizers. Nowadays hydrogen gains more attention mainly because, it is regarded as a future significant fuel by much of experts. The widespread use of hydrogen as source of energy could help to reduce the concern concerning the safety of energy, the total change of climate and the quality of air. Hydrogen is presented then as an excellent alternate initially and as substitute thereafter. It can play a role even more significant than conventional energies. Indeed, it has the advantage of being nonpolluting and it can use the same means of transport as conventional energies. For Algeria, it proves of importance capital. It not only makes it possible to increase and diversify its energy reserves and its exports but also to provide for its energy needs which become increasingly significant. Although hydrogen can be produced starting from a large variety of resources using a range of various technologies, the natural gas is generally preferred and will remain in the near future the principal primary product for the manufacture of hydrogen. Currently the most effective means of production of hydrogen is the Steam Reforming of Natural Gas (SMR). This process is seen as a one of principal technologies for the production of hydrogen. The disadvantages of this process it's that it consumes a great quantity of primary energy and that it releases in the atmosphere the gases that contribute to the warming of the plane. Among the alternatives processes of hydrogen production one can quote solar thermochemical processes. In this study, an exergetic analysis of the process of hydrogen production based on Zn/ZnO redox reactions is presented. In the first part of this study, an exergetic analysis is made for a temperature of the

Performance evaluation and comparison of fuel processors integrated with PEM fuel cell based on steam or autothermal reforming and on CO preferential oxidation or selective methanation

International Nuclear Information System (INIS)

Ercolino, Giuliana; Ashraf, Muhammad A.; Specchia, Vito; Specchia, Stefania

2015-01-01

Highlights: • Modeling of different fuel processors integrated with PEM fuel cell stack. • Steam or autothermal reforming + CO selective methanation or preferential oxidation. • Reforming of different hydrocarbons: gasoline, light diesel oil, natural gas. • 5 kW e net systems comparison via energy efficiency and primary fuel rate consumed. • Highest net efficiency: steam reformer + CO selective methanation based system. - Abstract: The performances of four different auxiliary power unit (APU) schemes, based on a 5 kW e net proton exchange membrane fuel cell (PEM-FC) stack, are evaluated and compared. The fuel processor section of each APU is characterized by a reformer (autothermal ATR or steam SR), a non-isothermal water gas shift (NI-WGS) reactor and a final syngas catalytic clean-up step: the CO preferential oxidation (PROX) reactor or the CO selective methanation (SMET) one. Furthermore, three hydrocarbon fuels, the most commonly found in service stations (gasoline, light diesel oil and natural gas) are considered as primary fuels. The comparison is carried out examining the results obtained by a series of steady-state system simulations in Aspen Plus® of the four different APU schemes by varying the fed fuel. From the calculated data, the performance of CO-PROX is not very different compared to that of the CO-SMET, but the performance of the SR based APUs is higher than the scheme of the ATR based APUs. The most promising APU scheme with respect to an overall performance target is the scheme fed with natural gas and characterized by a fuel processor chain consisting of SR, NI-WGS and CO-SMET reactors. This processing reactors scheme together with the fuel cell section, notwithstanding having practically the same energy efficiency of the scheme with SR, NI-WGS and CO-PROX reactors, ensures a less complex scheme, higher hydrogen concentration in the syngas, lower air mass rate consumption, the absence of nitrogen in the syngas and higher potential

Sorption-enhanced steam reforming of ethanol: thermodynamic comparison of CO{sub 2} sorbents

Energy Technology Data Exchange (ETDEWEB)

Wu, Y.J.; Santos, J.C.; Cunha, A.F.; Rodrigues, A.E. [University of Porto, Faculty of Engineering, Department of Chemical Engineering, Associated Laboratory LSRE/LCM, Laboratory of Separation and Reaction Engineering, Porto (Portugal); Diaz Alvarado, F.; Gracia, F. [Universidad de Chile, Facultad de Ingenieria, Departamento de Ingenieria Quimica y Biotecnologia, Laboratorio de Catalisis, Santiago (Chile)

2012-05-15

A thermodynamic analysis is performed with a Gibbs free energy minimization method to compare the conventional steam reforming of ethanol (SRE) process and sorption-enhanced SRE (SE-SRE) with three different sorbents, namely, CaO, Li{sub 2}ZrO{sub 3}, and hydrotalcite-like compounds (HTlc). As a result, the use of a CO{sub 2} adsorbent can enhance the hydrogen yield and provide a lower CO content in the product gas at the same time. The best performance of SE-SRE is found to be at 500 C with an HTlc sorbent. Nearly 6 moles hydrogen per mole ethanol can be produced, when the CO content in the vent stream is less than 10 ppm, so that the hydrogen produced via SE-SRE with HTlc sorbents can be directly used for fuel cells. Higher pressures do not favor the overall SE-SRE process due to lower yielding of hydrogen, although CO{sub 2} adsorption is enhanced. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Techno-economic prospects of small-scale membrane reactors in a future hydrogen-fuelled transportation sector

International Nuclear Information System (INIS)

Sjardin, M.; Damen, K.J.; Faaij, A.P.C.

2006-01-01

The membrane reactor is a novel technology for the production of hydrogen from natural gas. It promises economic small-scale hydrogen production, e.g. at refuelling stations and has the potential of inexpensive CO 2 separation. Four configurations of the membrane reactor have been modelled with Aspen plus to determine its thermodynamic and economic prospects. Overall energy efficiency is 84% HHV without H 2 compression (78% with compression up to 482bar). The modelling results also indicate that by using a sweep gas, the membrane reactor can produce a reformer exit stream consisting mainly of CO 2 and H 2 O (>90% mol ) suited for CO 2 sequestration after water removal with an efficiency loss of only 1% pt . Reforming with a 2MW membrane reactor (250 unit production volume) costs 14$/GJ H 2 including compression, which is more expensive than conventional steam reforming+compression (12$/GJ). It does, however, promise a cheap method of CO 2 separation, 14$/t CO 2 captured, due to the high purity of the exit stream. The well-to-wheel chain of the membrane reactor has been compared to centralised steam reforming to assess the trade-off between production scale and the construction of a hydrogen and a CO 2 distribution infrastructure. If the scale of centralised hydrogen production is below 40MW, the trade-off could be favourable for the membrane reactor with small-scale CO 2 capture (18$/GJ including H 2 storage, dispensing and CO 2 sequestration for 40MW SMR versus 19$/GJ for MR). The membrane reactor might become competitive with conventional steam reforming provided that thin membranes can be combined with high stability and a cheap manufacturing method for the membrane tubes. Thin membranes, industrial utility prices and larger production volumes (i.e. technological learning) might reduce the levelised hydrogen cost of the membrane reactor at the refuelling station to less than 14$/GJ including CO 2 sequestration cost, below that of large-scale H 2 production with

The Influence of oxide additives on Ni/Al2O3 catalysts in low temperature methane steam reforming

International Nuclear Information System (INIS)

Lazar, Mihaela; Dan, Monica; Mihet, Maria; Almasan, Valer

2009-01-01

Hydrogen is industrially produced by methane steam reforming. The process is catalytic and the usual catalyst is based on Ni as the active element. The main problem of this process is its inefficiency. It requires high temperatures at which Ni also favors the formation of graphite, which deactivates the catalysts. Ni has the advantage of being much cheaper than noble metal catalysts, so many researches are done in order to improve the properties of supported Ni catalysts and to decrease the temperature at which the process is energetically efficient. In order to obtain catalysts with high activity and stability, it is essential to maintain the dispersion of the active phase (Ni particles) and the stability of the support. Both properties can be improved by addition of a second oxide to the support. In this paper we present the results obtained in preparation and characterization of Ni/Al 2 O 3 catalysts modified by addition of CeO 2 and La 2 O 3 to alumina support. The following catalysts were prepared by impregnation method: Ni/Al 2 O 3 , Ni/CeO 2 -Al 2 O 3 and Ni/La 2 O 3 -Al 2 O 3 (10 wt.% Ni and 6 wt.% additional oxide). The catalytic surface was characterized by N 2 adsorption - desorption isotherms. The hydrogen - surface bond was characterized by Thermo-Programmed-Desorption (TPD) method. All catalysts were tested in steam reforming reaction of methane in the range of 600 - 700 deg. C, at atmospheric pressure working with CH 4 :H 2 O ratio of 1:3. The modified catalysts showed a better catalytic activity and selectivity for H 2 and CO 2 formation, at lower temperatures than the simple Ni/Al 2 O 3 catalyst. (authors)

Regulatory reforms and productivity: An empirical analysis of the Japanese electricity industry

International Nuclear Information System (INIS)

Nakano, Makiko; Managi, Shunsuke

2008-01-01

The Japanese electricity industry has experienced regulatory reforms since the mid-1990s. This article measures productivity in Japan's steam power-generation sector and examines the effect of reforms on the productivity of this industry over the period 1978-2003. We estimate the Luenberger productivity indicator, which is a generalization of the commonly used Malmquist productivity index, using a data envelopment analysis approach. Factors associated with productivity change are investigated through dynamic generalized method of moments (GMM) estimation of panel data. Our empirical analysis shows that the regulatory reforms have contributed to productivity growth in the steam power-generation sector in Japan

Zircon Supported Copper Catalysts for the Steam Reforming of Methanol

Science.gov (United States)

Widiastri, M.; Fendy, Marsih, I. N.

2008-03-01

Steam reforming of methanol (SRM) is known as one of the most favorable catalytic processes for producing hydrogen. Current research on zirconia, ZrO2 supported copper catalyst revealed that CuO/ZrO2 as an active catalyst for the SRM. Zircon, ZrSiO4 is available from the by-product of tin mining. In the work presented here, the catalytic properties of CuO/ZrSiO4 with various copper oxide compositions ranging from 2.70% (catalyst I), 4.12% (catalyst II), and 7.12%-mass (catalyst III), synthesized by an incipient wetness impregnation technique, were investigated to methanol conversion, selectivity towards CO formation, and effect of ZnO addition (7.83%CuO/8.01%ZnO/ZrSiO4 = catalyst V). The catalytic activity was obtained using a fixed bed reactor and the zircon supported catalyst activity was compared to those of CuO/ZnO/Al2O3 catalyst (catalyst IV) and commercial Kujang LTSC catalyst. An X-ray powder diffraction (XRD) analysis was done to identify the abundant phases of the catalysts. The catalysts topography and particle diameter were measured with scanning electron microscopy (SEM) and composition of the catalysts was measured by SEM-EDX, scanning electron microscope-energy dispersive using X-ray analysis. The results of this research provide information on the possibility of using zircon (ZrSiO4) as solid support for SRM catalysts.

Large scale sodium-water reaction tests for Monju steam generators

International Nuclear Information System (INIS)

Sato, M.; Hiroi, H.; Hori, M.

1976-01-01

To demonstrate the safe design of the steam generator system of the prototype fast reactor Monju against the postulated large leak sodium-water reaction, a large scale test facility SWAT-3 was constructed. SWAT-3 is a 1/2.5 scale model of the Monju secondary loop on the basis of the iso-velocity modeling. Two tests have been conducted in SWAT-3 since its construction. The test items using SWAT-3 are discussed, and the description of the facility and the test results are presented

Steam reforming: an old process for a new solution; Le vaporeformage catalytique: un vieux procede pour une solution nouvelle...

Energy Technology Data Exchange (ETDEWEB)

Aupretre, F.; Descorme, C.; Duprez, D. [Poitiers Univ., Lab. de Catalyse en Chimie Organique, LACCO, UMR CNRS 6503, 86 (France)

2000-07-01

A bibliographic review allows to understand very quickly the stake that the electric-powered vehicle represents. The research of a hydrogen production process answering to the demands of the fuel cell application is then one of the main stakes. The catalytic steam reforming of hydrocarbons or of alcohols is a very promising way. The choices of ethanol and of rhodium based catalysts supported on oxides with strong oxygen mobility will be entirely justified because of the physico-chemical characteristics of the ethanol, of the reaction mechanism, of the cerium based oxide catalyst and of the specifications involved in the fuel cell application. (O.M.)

Catalyst Deactivation and Regeneration in Low Temperature Ethanol Steam Reforming with Rh/CeO2-ZrO2 Catalysts

Energy Technology Data Exchange (ETDEWEB)

Roh, Hyun-Seog; Platon, Alex; Wang, Yong; King, David L.

2006-08-01

Rh/CeO2-ZrO2 catalysts with various CeO2/ZrO2 ratios have been applied to H2 production from ethanol steam reforming at low temperatures. The catalysts all deactivated with time on stream (TOS) at 350 C. The addition of 0.5% K has a beneficial effect on catalyst stability, while 5% K has a negative effect on catalytic activity. The catalyst could be regenerated considerably even at ambient temperature and could recover its initial activity after regeneration above 200 C with 1% O2. The results are most consistent with catalyst deactivation due to carbonaceous deposition on the catalyst.

Scaled parametric equation of state for steam in the critical region

International Nuclear Information System (INIS)

Murphy, T.A.; Sengers, J.V.

1975-01-01

The anomalous thermodynamic behavior of fluids near the critical point can be described in terms of scaling laws. In recent years a parametric equation of state, the so-called Linear Model, has been proposed that satisfies the scaling laws and contains only a small number of adjustable parameters. It is shown that the Linear Model yields a satisfactory representation of the experimental P-V-T data for steam in the critical region. (29 references)

Upgrading of reformate gas for different applications with focus on small-scale hydrogen production

Energy Technology Data Exchange (ETDEWEB)

Jannasch, Anna-Karin; Silversand, Fredrik [CATATOR AB, Lund (Sweden)

2004-12-01

Hydrogen gas or hydrogen rich gas is today used in many different applications, i.e. as fuel in fuel cells or additive in vehicle fuel (i.e. hythane) and as reagent or reducing agent in different industrial product lines. The majority of the hydrogen is produced either via electrolysis or reformation, where this work has entirely been focused on the latter alternative. The overarching aims of this project have been to demonstrate the need for reformate purification for different applications, and then, to investigate different available methods that can be used in order to enable the requested gas clean-up. The different purification methods have been examined with respect to parameters such as operating conditions (temperature, pressure), impurity tolerance, size, weight and cost. Another goal of the project has been to investigate how the reformer fuel type used influences the reformate gas quality and hence, the need for gas purification before the reformate can be fed to e.g. a low temperature polymer membrane fuel cell (PEMFC). For this reason, some experimental work has been performed. First, analysis of the reformate gas composition when natural gas, LPG, gasoline, diesel, kerosene (low and high S-concentration (i.e. JP8)) and ethanol have been processed. The reformation tests were carried out in a small scale reformer unit ({approx} 1 kW H{sub 2}) including Catator's catalyst formulations developed for the steam reforming, the water gas shift and the preferential oxidation reaction, respectively. Verification tests, with synthetic gas blends, including different potential reformate impurities, and with real reformate gas were thereafter performed with a commercial 4-cell PEMFC stack (3-5 W). Finally, some examination and also to some extent further development of Catator's existing gas purification units were made, i.e. chemical (WGS, PROX) and physical (regenerative adsorption). The Pd-alloy membrane seems to be the obvious choice of purification

High temperature nuclear heat for isothermal reformer

International Nuclear Information System (INIS)

Epstein, M.

2000-01-01

High temperature nuclear heat can be used to operate a reformer with various feedstock materials. The product synthesis gas can be used not only as a source for hydrogen and as a feedstock for many essential chemical industries, such as ammonia and other products, but also for methanol and synthetic fuels. It can also be burnt directly in a combustion chamber of a gas turbine in an efficient combined cycle and generate electricity. In addition, it can be used as fuel for fuel cells. The reforming reaction is endothermic and the contribution of the nuclear energy to the calorific value of the final product (synthesis gas) is about 25%, compared to the calorific value of the feedstock reactants. If the feedstock is from fossil origin, the nuclear energy contributes to a substantial reduction in CO 2 emission to the atmosphere. The catalytic steam reforming of natural gas is the most common process. However, other feedstock materials, such as biogas, landfill gas and CO 2 -contaminated natural gas, can be reformed as well, either directly or with the addition of steam. The industrial steam reformers are generally fixed bed reactors, and their performance is strongly affected by the heat transfer from the furnace to the catalyst tubes. In top-fired as well as side-fired industrial configurations of steam reformers, the radiation is the main mechanism of heat transfer and convection heat transfer is negligible. The flames and the furnace gas constitute the main sources of the heat. In the nuclear reformers developed primarily in Germany, in connection with the EVA-ADAM project (closed cycle), the nuclear heat is transferred from the nuclear reactor coolant gas by convection, using a heating jacket around the reformer tubes. In this presentation it is proposed that the helium in a secondary loop, used to cool the nuclear reactor, will be employed to evaporate intermediate medium, such as sodium, zinc and aluminum chloride. Then, the vapors of the medium material transfer

System requirements of diesel reforming for the SOFC

International Nuclear Information System (INIS)

Harasti, P.T.; Amphlett, J.C.; Mann, R.F.; Peppley, B.A.; Thurgood, C.P.

2003-01-01

Diesel fuels are currently a very attractive source of hydrogen due to the global infrastructure for production and distribution that exists today. In order to extract the hydrogen, the hydrocarbon molecules must be chemically reformed into manageable, hydrogen-rich product gases that can be directly used in electrochemical energy conversion devices such as fuel cells. High temperature fuel cells are particularly attractive for diesel-fuelled systems due to the possibility of thermal integration with the high temperature reformer. The methods available for diesel fuel processing are: Steam Reforming, Partial Oxidation, and Auto-Thermal Reforming. The latter two methods introduce air into the process in order to cause exothermic oxidation reactions, which complement the endothermic heating requirement of the reforming reactions. This helps to achieve the high temperature required, but also introduces nitrogen, which can yield unwanted NO x emissions. The components of the reformer should include: an injection system to mix and vaporize the diesel fuel and steam while avoiding the formation of carbon deposits inside the reactor; a temperature and heat management system; and a method of sulphur removal. This presentation will discuss the operating conditions and design requirements of a diesel fuel processor for a solid oxide fuel cell (SOFC) system. (author)

Assessing the Life-Cycle Performance of Hydrogen Production via Biofuel Reforming in Europe

OpenAIRE

Susmozas, Ana; Iribarren, Diego; Dufour, Javier

2015-01-01

Currently, hydrogen is mainly produced through steam reforming of natural gas. However, this conventional process involves environmental and energy security concerns. This has led to the development of alternative technologies for (potentially) green hydrogen production. In this work, the environmental and energy performance of biohydrogen produced in Europe via steam reforming of glycerol and bio-oil is evaluated from a life-cycle perspective, and contrasted with that of conventional hydroge...

Large-Scale Curriculum Reform in Finland--Exploring the Interrelation between Implementation Strategy, the Function of the Reform, and Curriculum Coherence

Science.gov (United States)

Pietarinen, Janne; Pyhältö, Kirsi; Soini, Tiina

2017-01-01

The study aims to gain a better understanding of the national large-scale curriculum process in terms of the used implementation strategies, the function of the reform, and the curriculum coherence perceived by the stakeholders accountable in constructing the national core curriculum in Finland. A large body of school reform literature has shown…

Enabling and challenging factors in institutional reform: The case of SCALE-UP

Science.gov (United States)

Foote, Kathleen; Knaub, Alexis; Henderson, Charles; Dancy, Melissa; Beichner, Robert J.

2016-06-01

While many innovative teaching strategies exist, integration into undergraduate science teaching has been frustratingly slow. This study aims to understand the low uptake of research-based instructional innovations by studying 21 successful implementations of the Student Centered Active Learning with Upside-down Pedagogies (SCALE-UP) instructional reform. SCALE-UP significantly restructures the classroom environment and pedagogy to promote highly active and interactive instruction. Although originally designed for university introductory physics courses, SCALE-UP has spread to many other disciplines at hundreds of departments around the world. This study reports findings from in-depth, open-ended interviews with 21 key contact people involved with successful secondary implementations of SCALE-UP throughout the United States. We defined successful implementations as those who restructured their pedagogy and classroom and sustained and/or spread the change. Interviews were coded to identify the most common enabling and challenging factors during reform implementation and compared to the theoretical framework of Kotter's 8-step Change Model. The most common enabling influences that emerged are documenting and leveraging evidence of local success, administrative support, interaction with outside SCALE-UP user(s), and funding. Many challenges are linked to the lack of these enabling factors including difficulty finding funding, space, and administrative and/or faculty support for reform. Our focus on successful secondary implementations meant that most interviewees were able to overcome challenges. Presentation of results is illuminated with case studies, quotes, and examples that can help secondary implementers with SCALE-UP reform efforts specifically. We also discuss the implications for policy makers, researchers, and the higher education community concerned with initiating structural change.

Bench Scale Process for Low Cost CO₂ Capture Using a Phase-Changing Absorbent: Final Scientific/Technical Report

Energy Technology Data Exchange (ETDEWEB)

Westendorf, Tiffany [GE Global Research, Niskayuna, New York (United States); Buddle, Stanlee [GE Global Research, Niskayuna, New York (United States); Caraher, Joel [GE Global Research, Niskayuna, New York (United States); Chen, Wei [GE Global Research, Niskayuna, New York (United States); Doherty, Mark [GE Global Research, Niskayuna, New York (United States); Farnum, Rachel [GE Global Research, Niskayuna, New York (United States); Giammattei, Mark [GE Global Research, Niskayuna, New York (United States); Hancu, Dan [GE Global Research, Niskayuna, New York (United States); Miebach, Barbara [GE Global Research, Niskayuna, New York (United States); Perry, Robert [GE Global Research, Niskayuna, New York (United States); Rubinsztajn, Gosia; Spiry, Irina; Wilson, Paul; Wood, Benjamin

2017-05-31

The objective of this project is to design and build a bench-scale process for a novel phase-changing aminosilicone-based CO₂-capture solvent. The project will establish scalability and technical and economic feasibility of using a phase-changing CO₂-capture absorbent for post-combustion capture of CO₂ from coal-fired power plants. The U.S. Department of Energy’s goal for Transformational Carbon Capture Technologies is the development of technologies available for demonstration by 2025 that can capture 90% of emitted CO₂ with at least 95% CO₂ purity for less than $40/tonne of CO₂ captured. In the first budget period of the project, the bench-scale phase-changing CO2 capture process was designed using data and operating experience generated under a previous project (ARPA-e project DE-AR0000084). Sizing and specification of all major unit operations was completed, including detailed process and instrumentation diagrams. The system was designed to operate over a wide range of operating conditions to allow for exploration of the effect of process variables on CO₂ capture performance. In the second budget period of the project, individual bench-scale unit operations were tested to determine the performance of each of each unit. Solids production was demonstrated in dry simulated flue gas across a wide range of absorber operating conditions, with single stage CO₂ conversion rates up to 75mol%. Desorber operation was demonstrated in batch mode, resulting in desorption performance consistent with the equilibrium isotherms for GAP-0/CO₂ reaction. Important risks associated with gas humidity impact on solids consistency and desorber temperature impact on thermal degradation were explored, and adjustments to the bench-scale process were made to address those effects. Corrosion experiments were conducted to support selection of suitable materials of construction for the major

Modelagem de um reator integral aplicado na reação de reforma a vapor de metano = Modeling of integral reactor applied methane steam reforming

Directory of Open Access Journals (Sweden)

Giane Gonçalves

2007-07-01

Full Text Available Freqüentemente, a validação de modelos matemáticos aplicados a reatores industriais esbarra na dificuldade de obtenção de medidas experimentais confiáveis. Uma maneira de contornar esta limitação corresponde à implantação de uma unidade em escala de bancada devidamente instrumentada, na qual são obtidos dados experimentais emcondições controladas. Neste contexto, foram efetuados ensaios em um reator integral de reforma a vapor de metano em escala de bancada, em diversas condições experimentais. As medidas de temperatura no leito foram efetuadas por meio de um termopar multiponto em seis posições axiais distintas, enquanto a composição do efluente do reator foi determinada por cromatografia gasosa. Estes dados experimentais foram comparados com as previsões de um modelo pseudo-homogêneo, unidimensional e dinâmico. Os resultados indicam que o modelo é adequado, sendo que tanto a atividade catalítica como a conversão são sensíveis à temperatura operacional, enquanto a temperatura do leito é praticamente insensível à vazão nas condições experimentais exploradas.Frequently, the validation of applied mathematical models of industrial reactors dash into the difficulty of obtaining reliable experimental data. A way to overcome this limitation is the proper use and operation or a in bench scale, experimental setup from whichexperimental data can be obtained in controlled conditions. In this context, experiments were carried out in an integral reactor of steam reform, in different experimental conditions. Thermocouples were placed along the catalyst bed to allow for temperature monitoring in six equally spaced and distinct positions of the reactor, the composition of the effluent of the reactor was determined by gas chromatography. These experimental data were compared with the theoretical results of a pseudo-homogeneous one-dimensional,dynamic mathematical model. The results indicate that the model can successfully

Evaluation of malodor for automobile air conditioner evaporator by using laboratory-scale test cooling bench.

Science.gov (United States)

Kim, Kyung Hwan; Kim, Sun Hwa; Jung, Young Rim; Kim, Man Goo

2008-09-12

As one of the measures to improve the environment in an automobile, malodor caused by the automobile air-conditioning system evaporator was evaluated and analyzed using laboratory-scale test cooling bench. The odor was simulated with an evaporator test cooling bench equipped with an airflow controller, air temperature and relative humidity controller. To simulate the same odor characteristics that occur from automobiles, one previously used automobile air conditioner evaporator associated with unpleasant odors was selected. The odor was evaluated by trained panels and collected with aluminum polyester bags. Collected samples were analyzed by thermal desorption into a cryotrap and subsequent gas chromatographic separation, followed by simultaneous olfactometry, flame ionization detector and identified by atomic emission detection and mass spectrometry. Compounds such as alcohols, aldehydes, and organic acids were identified as responsible odor-active compounds. Gas chromatography/flame ionization detection/olfactometry combined sensory method with instrumental analysis was very effective as an odor evaluation method in an automobile air-conditioning system evaporator.

Parametric study on the steam reforming of phenol-PET solution to hydrogen production over Ni promoted on Al_2O_3-La_2O_3 catalyst

International Nuclear Information System (INIS)

Nabgan, Bahador; Nabgan, Walid; Tuan Abdullah, Tuan Amran; Tahir, Muhammad; Gambo, Yahya; Ibrahim, Maryam; Syie Luing, Wong

2017-01-01

Highlights: • Parametric study of H_2 production from phenol-PET steam reforming was studied. • Optimised conditions were 800 °C, 0.10 ml/min feed flow rate, and 7% PET. • High amount of aliphatic branched-chains and cyclic compounds were produced. • PET was efficiently converted to hydrogen and valuable fuels at optimized condition. • Significant influence resulted for all the main independent factors. - Abstract: Production of hydrogen from plastic waste could be a prospective key to the ecological problems resulted from waste. To further explore the process, a 32-runs parametric study on the steam reforming of Polyethylene terephthalate (PET) dissolved in phenol was conducted in a fixed bed reactor using Ni over La_2O_3-Al_2O_3 support. The five factors studied were temperature (A), feed flow rate (B), mass flow (C), phenol concentration (D), and concentration of PET solution (E), whereas the responses were phenol conversion (Y_1) and hydrogen selectivity (Y_2). From the result, it was observed that significant influence resulted for all the main independent variables on the dependent variable of Y_1 and Y_2 with the range of 47.24–97.6% and 49–70.96%, respectively. Moreover, the Y_1 and Y_2 responses have influenced by some interaction variables like AC, CD, CE, ACE, and BCE. As evident from the design, initial variables such as 800 °C, 0.10 ml/min feed flow rate, 10 SCCM mass flow, 10 wt.% of phenol in the feed, and 7% PET concentration were the best preliminary conditions that formed maximum Y_1 (94%) and Y_2 (71%) responses. However, analyses on the product composition revealed that high amount of aliphatic branched-chains along with moderate amount of cyclic compounds were produced from steam reforming of PET-phenol. Due to the short retention time of the compounds on the catalysts bed, the aromatization of PET cracking products was small.

Computational Investigation of the Thermochemistry and Kinetics of Steam Methane Reforming Over a Multi-Faceted Nickel Catalyst

KAUST Repository

Blaylock, D. Wayne

2011-08-20

A microkinetic model of steam methane reforming over a multi-faceted nickel surface using planewave, periodic boundary condition density functional theory is presented. The multi-faceted model consists of a Ni(111) surface, a Ni(100) surface, and nickel step edge sites that are modeled as a Ni(211) surface. Flux and sensitivity analysis are combined to gain an increased understanding of the important reactions, intermediates, and surface facets in SMR. Statistical thermodynamics are applied to allow for the investigation of SMR under industrially-relevant conditions (e.g., temperatures in excess of 500 °C and pressures in excess of 1 bar). The most important surface reactions are found to occur at the under-coordinated step edge sites modeled using the Ni(211) surface as well as on the Ni(100) surface. The primary reforming pathway is predicted to be through C*+ O*→ CO*at high temperatures; however, hydrogen-mediated reactions such as C*+ OH*→ COH*and C.H.*+ O*→ CHO*are predicted to become more important at low temperatures. The rate-limiting reactions are predicted to be dissociative chemisorption of methane in addition to the aforementioned C-O addition reactions. © 2011 Springer Science+Business Media, LLC.

Investigation of the promoting effect of Mn on a Pt/C catalyst for the steam and aqueous phase reforming of glycerol

Energy Technology Data Exchange (ETDEWEB)

Bossola, Filippo; Pereira-Hernández, Xavier Isidro; Evangelisti, Claudio; Wang, Yong; Dal Santo, Vladimiro

2017-05-01

The catalytic performances in steam reforming (SR) and aqueous phase reforming (APR) of glycerol of a bimetallic Pt-Mn catalyst supported on activated carbon are investigated and correlated with the surface properties of the catalyst. Under SR conditions, Mn showed a significant promoting effect over Pt/C, both in terms of hydrogen production rate and conversion, with a higher selectivity toward the glycerol dehydration products. Upon addition of Mn the amount of strong Lewis acid sites increased, promoting the dehydration of glycerol and favoring the CAO over CAC cleavage at expenses of hydrogen selectivity. Conversely, under APR conditions, a slightly higher hydrogen selectivity and only minimal enhancement in hydrogen production were found, while the products selectivity was comparable to Pt/C. Most of Mn leached into the aqueous media, but the remaining (<5% of the fresh parent sample) might be alloyed with Pt and promote the CO desorption from neighbor Pt sites.

Reforming options for hydrogen production from fossil fuels for PEM fuel cells

Energy Technology Data Exchange (ETDEWEB)

Ersoz, Atilla; Olgun, Hayati [TUBITAK Marmara Research Center, Institute of Energy, Gebze, 41470 Kocaeli (Turkey); Ozdogan, Sibel [Marmara University Faculty of Engineering, Goztepe, 81040 Istanbul (Turkey)

2006-03-09

PEM fuel cell systems are considered as a sustainable option for the future transport sector in the future. There is great interest in converting current hydrocarbon based transportation fuels into hydrogen rich gases acceptable by PEM fuel cells on-board of vehicles. In this paper, we compare the results of our simulation studies for 100kW PEM fuel cell systems utilizing three different major reforming technologies, namely steam reforming (SREF), partial oxidation (POX) and autothermal reforming (ATR). Natural gas, gasoline and diesel are the selected hydrocarbon fuels. It is desired to investigate the effect of the selected fuel reforming options on the overall fuel cell system efficiency, which depends on the fuel processing, PEM fuel cell and auxiliary system efficiencies. The Aspen-HYSYS 3.1 code has been used for simulation purposes. Process parameters of fuel preparation steps have been determined considering the limitations set by the catalysts and hydrocarbons involved. Results indicate that fuel properties, fuel processing system and its operation parameters, and PEM fuel cell characteristics all affect the overall system efficiencies. Steam reforming appears as the most efficient fuel preparation option for all investigated fuels. Natural gas with steam reforming shows the highest fuel cell system efficiency. Good heat integration within the fuel cell system is absolutely necessary to achieve acceptable overall system efficiencies. (author)

Reforming options for hydrogen production from fossil fuels for PEM fuel cells

Science.gov (United States)

Ersoz, Atilla; Olgun, Hayati; Ozdogan, Sibel

PEM fuel cell systems are considered as a sustainable option for the future transport sector in the future. There is great interest in converting current hydrocarbon based transportation fuels into hydrogen rich gases acceptable by PEM fuel cells on-board of vehicles. In this paper, we compare the results of our simulation studies for 100 kW PEM fuel cell systems utilizing three different major reforming technologies, namely steam reforming (SREF), partial oxidation (POX) and autothermal reforming (ATR). Natural gas, gasoline and diesel are the selected hydrocarbon fuels. It is desired to investigate the effect of the selected fuel reforming options on the overall fuel cell system efficiency, which depends on the fuel processing, PEM fuel cell and auxiliary system efficiencies. The Aspen-HYSYS 3.1 code has been used for simulation purposes. Process parameters of fuel preparation steps have been determined considering the limitations set by the catalysts and hydrocarbons involved. Results indicate that fuel properties, fuel processing system and its operation parameters, and PEM fuel cell characteristics all affect the overall system efficiencies. Steam reforming appears as the most efficient fuel preparation option for all investigated fuels. Natural gas with steam reforming shows the highest fuel cell system efficiency. Good heat integration within the fuel cell system is absolutely necessary to achieve acceptable overall system efficiencies.

Assessing the Life-Cycle Performance of Hydrogen Production via Biofuel Reforming in Europe

Directory of Open Access Journals (Sweden)

Ana Susmozas

2015-06-01

Full Text Available Currently, hydrogen is mainly produced through steam reforming of natural gas. However, this conventional process involves environmental and energy security concerns. This has led to the development of alternative technologies for (potentially green hydrogen production. In this work, the environmental and energy performance of biohydrogen produced in Europe via steam reforming of glycerol and bio-oil is evaluated from a life-cycle perspective, and contrasted with that of conventional hydrogen from steam methane reforming. Glycerol as a by-product from the production of rapeseed biodiesel and bio-oil from the fast pyrolysis of poplar biomass are considered. The processing plants are simulated in Aspen Plus® to provide inventory data for the life cycle assessment. The environmental impact potentials evaluated include abiotic depletion, global warming, ozone layer depletion, photochemical oxidant formation, land competition, acidification and eutrophication. Furthermore, the cumulative (total and non-renewable energy demand is calculated, as well as the corresponding renewability scores and life-cycle energy balances and efficiencies of the biohydrogen products. In addition to quantitative evidence of the (expected relevance of the feedstock and impact categories considered, results show that poplar-derived bio-oil could be a suitable feedstock for steam reforming, in contrast to first-generation bioglycerol.

Hydrogen production by steam reforming of bio-oil aqueous fraction over Co-Fe/ZSM-5

Science.gov (United States)

Chen, Mingqiang; Wang, Yishuang; Liang, Tian; Yang, Zhonglian

2018-02-01

A series of Co-Fe/ZSM-5 catalysts were prepared by impregnation method and their catalytic performance under steam reforming bio-oil aqueous fraction (SRBAF). The as-prepared catalysts were characterized by XRD, BET, and SEM. The characterization results revealed the Co-Fe alloy phase was formed in Co0.5Fe0.5/ZSM-5 catalyst, and this catalyst exhibited unique pore volume (0.28 cm3/g) and pore size (8.4 nm). The results of experiment demonstrated the addition of Fe species could significantly increase C conversion and H2 yield, and the formation of Co-Fe alloy effectively inhibited methanation reaction and improved water-gas shift (WGS) reaction. The highest H2 yield (81%) and C conversion (85%) was obtained at the following reaction conditions: 2.5 g of C0.5F0.5/Z catalyst, T = 700 °C, S/C = 10-14,.feed flow rate was 10.0 gbio-oil/h, N2 flow rate was 0.16 L/min.

Steam reforming of fuel to hydrogen in fuel cells

Science.gov (United States)

Fraioli, Anthony V.; Young, John E.

1984-01-01

A fuel cell capable of utilizing a hydrocarbon such as methane as fuel and having an internal dual catalyst system within the anode zone, the dual catalyst system including an anode catalyst supporting and in heat conducting relationship with a reforming catalyst with heat for the reforming reaction being supplied by the reaction at the anode catalyst.

Effect of microwave double absorption on hydrogen generation from methanol steam reforming

Energy Technology Data Exchange (ETDEWEB)

Chen, Wei-Hsin; Lin, Bo-Jhih [Department of Greenergy, National University of Tainan, Tainan 700 (China)

2010-03-15

Hydrogen generation from steam reforming of methanol (SRM) with a CuO/ZnO/Al{sub 2}O{sub 3} catalyst was investigated in the study; particular emphasis was placed on the reactions of SRM exposed to an environment with microwave irradiation. By virtue of the double absorption of microwaves by both the reagents and the catalyst, the experiments suggested that the SRM could be heated and triggered rapidly within a short time, and the methanol conversion from SRM with microwave heating was high compared to that with conventional heating. The obtained results also indicated that, when the reaction temperature was as high as 250 C, thermodynamic equilibrium governed the SRM, whereas the reaction was kinetically controlled for the temperature lower than 250 C. Contrary to Le Chatelier's principle, it was noted that an increase in S/C ratio decreased methanol conversion. This can be explained by the fact that water absorbs microwave irradiation stronger than methanol. The performance of the SRM was evaluated based on the carbon conservation method and the nitrogen tracer method. It was found that the latter was also capable of providing an accurate prediction on methanol conversion, even though the flow rate of the product gas was not measured. (author)

Stability, carbon resistance, and reactivity toward autothermal reforming of nickel on ceria-based supports

International Nuclear Information System (INIS)

Sutthisripok, W.; Laosiripojana, N.

2004-01-01

'Full text:' Solid Oxide Fuel Cell (SOFC) normally requires a reformer unit, where the fuel such as natural gas, methane, methanol, or ethanol can be reformed to hydrogen before introducing to the main part of fuel cell. Nickel on commercial supports such as Al2O3, MgO, ZrO2 has been widely reported to be used as the reforming catalyst commercially. Carbon formation and catalyst deactivation are always the main problems of using this type of catalyst. It is well established that CeO2 and CeO2-ZrO2 have been applied as the catalysts in a wide variety of reactions involving oxidation or partial oxidation of hydrocarbons (e.g. automotive catalysis). In order to quantify the performance of nickel on CeO2 and CeO2-ZrO2 supports for reformer application, the stabilities toward methane steam reforming and the carbon formation resistance were studied. After 18 hours, nickel on CeO2-ZrO2 with the Ce/Zr ratio of 3/1 presented the best performance in term of stability and activity. It also provided excellent resistance toward carbon formation compared to commercial Ni/Al2O3. The autothermal reforming of methane over Ni catalyst on CeO2 and CeO2-ZrO2 supports were also investigated. Ni/Ce-ZrO2 with the Ce/ Zr ratio of 3/1 also showed the best performance. The kinetics of this reaction was also studied. In the temperature range of 750-900C, the reaction order in methane was always closed to 1. The catalyst showed a slight positive effect of hydrogen and a negative effect of steam on the steam reforming rate. The addition of oxygen increased the steam reforming rate. However, the productions of CO and H2 decreased with increasing oxygen partial pressure. (author)

Coal flotation - bench-scale study. Flotacao de carvao estudo em escala de bancada

Energy Technology Data Exchange (ETDEWEB)

Campos, A.R. de; Almeida, S L.M. de; Santos, A.T. dos

1979-01-01

Run-of-mine coal and pre-washed coal from Santa Catarina, Brazil, were characterized using washability curves and by particle size analysis after crushing. Bench-scale froth flotation tests were then conducted with the pre-washed coal. Kerosene and diesel oil were used as the collectors, and pine oil as the frother. The influence of starch (as depressor) on flotation was also studied. The effects of feed particle size, pH, collector addition, frother addition, depressor addition and flotation time were investigated. A 9.5% ash content coal could be obtained with a mass recovery of about 29%. (17 refs.)

Investigating the Plasma-Assisted and Thermal Catalytic Dry Methane Reforming for Syngas Production: Process Design, Simulation and Evaluation

Directory of Open Access Journals (Sweden)

Evangelos Delikonstantis

2017-09-01

Full Text Available The growing surplus of green electricity generated by renewable energy technologies has fueled research towards chemical industry electrification. By adapting power-to-chemical concepts, such as plasma-assisted processes, cheap resources could be converted into fuels and base chemicals. However, the feasibility of those electrified processes at large scale has not been investigated yet. Thus, the current work strives to compare, for first time in the literature, plasma-assisted production of syngas, from CH4 and CO2 (dry methane reforming, with thermal catalytic dry methane reforming. Specifically, both processes are conceptually designed to deliver syngas suitable for methanol synthesis (H2/CO ≥ 2 in mole. The processes are simulated in the Aspen Plus process simulator where different process steps are investigated. Heat integration and equipment cost estimation are performed for the most promising process flow diagrams. Collectively, plasma-assisted dry methane reforming integrated with combined steam/CO2 methane reforming is an effective way to deliver syngas for methanol production. It is more sustainable than combined thermal catalytic dry methane reforming with steam methane reforming, which has also been proposed for syngas production of H2/CO ≥ 2; in the former process, 40% more CO2 is captured, while 38% less H2O is consumed per mol of syngas. Furthermore, the plasma-assisted process is less complex than the thermal catalytic one; it requires higher amount of utilities, but comparable capital investment.

High-temperature hydrogen-air-steam detonation experiments in the BNL small-scale development apparatus

International Nuclear Information System (INIS)

Ciccarelli, G.; Ginsburg, T.; Boccio, J.; Economos, C.; Finfrock, C.; Gerlach, L.; Sato, K.; Kinoshita, M.

1994-08-01

The Small-Scale Development Apparatus (SSDA) was constructed to provide a preliminary set of experimental data to characterize the effect of temperature on the ability of hydrogen-air-steam mixtures to undergo detonations and, equally important, to support design of the larger scale High-Temperature Combustion Facility (HTCF) by providing a test bed for solution of a number of high-temperature design and operational problems. The SSDA, the central element of which is a 10-cm inside diameter, 6.1-m long tubular test vessel designed to permit detonation experiments at temperatures up to 700K, was employed to study self-sustained detonations in gaseous mixtures of hydrogen, air, and steam at temperatures between 300K and 650K at a fixed initial pressure of 0.1 MPa. Hydrogen-air mixtures with hydrogen composition from 9 to 60 percent by volume and steam fractions up to 35 percent by volume were studied for stoichiometric hydrogen-air-steam mixtures. Detonation cell size measurements provide clear evidence that the effect of hydrogen-air gas mixture temperature, in the range 300K-650K, is to decrease cell size and, hence, to increase the sensitivity of the mixture to undergo detonations. The effect of steam content, at any given temperature, is to increase the cell size and, thereby, to decrease the sensitivity of stoichiometric hydrogen-air mixtures. The hydrogen-air detonability limits for the 10-cm inside diameter SSDA test vessel, based upon the onset of single-head spin, decreased from 15 percent hydrogen at 300K down to between 9 and 10 percent hydrogen at 650K. The one-dimensional ZND model does a very good job at predicting the overall trends in the cell size data over the range of hydrogen-air-steam mixture compositions and temperature studied in the experiments

An Isothermal Steam Expander for an Industrial Steam Supplying System

Directory of Open Access Journals (Sweden)

Chen-Kuang Lin

2015-01-01

Full Text Available Steam is an essential medium used in the industrial process. To ensure steam quality, small and middle scale boilers are often adopted. However, because a higher steam pressure (compared to the necessary steam pressure is generated, the boiler’s steam pressure will be reduced via a pressure regulator before the steam is directed through the process. Unfortunately, pressure is somewhat wasted during the reducing process. Therefore, in order to promote energy efficiency, a pressure regulator is replaced by a steam expander. With this steam expander, the pressure will be transformed into mechanical energy and extracted during the expansion process. A new type of isothermal steam expander for an industrial steam supplying system will be presented in the paper. The isothermal steam expander will improve the energy efficiency of a traditional steam expander by replacing the isentropic process with an isothermal expansion process. With this, steam condensation will decrease, energy will increase, and steam quality will be improved. Moreover, the mathematical model of the isothermal steam expander will be established by using the Schmidt theory, the same principle used to analyze Stirling engines. Consequently, by verifying the correctness of the theoretical model for the isothermal steam expander using experimental data, a prototype of 100 c.c. isothermal steam expander is constructed.

High Activity of Ce1-xNixO2-y for H2 Production through Ethanol Steam Reforming: Tuning Catalytic Performance through Metal-Oxide Interactions

Energy Technology Data Exchange (ETDEWEB)

G Zhou; L Barrio; S Agnoli; S Senanayake; J Evans; A Kubacka; M Estrella; J Hanson; A Martinez-Arias; et al.

2011-12-31

The importance of the oxide: Ce{sub 0.8}Ni{sub 0.2}O{sub 2-y} is an excellent catalyst for ethanol steam reforming. Metal-oxide interactions perturb the electronic properties of the small particles of metallic nickel present in the catalyst under the reaction conditions and thus suppress any methanation activity. The nickel embedded in ceria induces the formation of O vacancies, which facilitate cleavage of the OH bonds in ethanol and water.

Energy and exergy analysis of an ethanol reforming process for solid oxide fuel cell applications.

Science.gov (United States)

Tippawan, Phanicha; Arpornwichanop, Amornchai

2014-04-01

The fuel processor in which hydrogen is produced from fuels is an important unit in a fuel cell system. The aim of this study is to apply a thermodynamic concept to identify a suitable reforming process for an ethanol-fueled solid oxide fuel cell (SOFC). Three different reforming technologies, i.e., steam reforming, partial oxidation and autothermal reforming, are considered. The first and second laws of thermodynamics are employed to determine an energy demand and to describe how efficiently the energy is supplied to the reforming process. Effect of key operating parameters on the distribution of reforming products, such as H2, CO, CO2 and CH4, and the possibility of carbon formation in different ethanol reformings are examined as a function of steam-to-ethanol ratio, oxygen-to-ethanol ratio and temperatures at atmospheric pressure. Energy and exergy analysis are performed to identify the best ethanol reforming process for SOFC applications. Copyright © 2014 Elsevier Ltd. All rights reserved.

Bench-scale testing of a micronized magnetite, fine-coal cleaning process

Energy Technology Data Exchange (ETDEWEB)

Suardini, P.J. [Custom Coals, International, Pittsburgh, PA (United States)

1995-11-01

Custom Coals, International has installed and is presently testing a 500 lb/hr. micronized-magnetite, fine-coal cleaning circuit at PETC`s Process Research Facility (PRF). The cost-shared project was awarded as part of the Coal Preparation Program`s, High Efficiency Preparation Subprogram. The project includes design, construction, testing, and decommissioning of a fully-integrated, bench-scale circuit, complete with feed coal classification to remove the minus 30 micron slimes, dense medium cycloning of the 300 by 30 micron feed coal using a nominal minus 10 micron size magnetite medium, and medium recovery using drain and rinse screens and various stages and types of magnetic separators. This paper describes the project circuit and goals, including a description of the current project status and the sources of coal and magnetite which are being tested.

Influence of Gold on Ce-Zr-Co Fluorite-Type Mixed Oxide Catalysts for Ethanol Steam Reforming

Directory of Open Access Journals (Sweden)

Véronique Pitchon

2012-02-01

Full Text Available The effect of gold presence on carbon monoxide oxidation and ethanol steam reforming catalytic behavior of two Ce-Zr-Co mixed oxides catalysts with a constant Co charge and different Ce/Zr ratios was investigated. The Ce-Zr-Co mixed oxides were obtained by the pseudo sol-gel like method, based on metallic propionates polymerization and thermal decomposition, whereas the gold-supported Ce-Zr-Co mixed oxides catalysts were prepared using the direct anionic exchange. The catalysts were characterized using XRD, TPR, and EDXS-TEM. The presence of Au in doped Ce-Zr-Co oxide catalyst decreases the temperature necessary to reduce the cobalt and the cerium loaded in the catalyst and favors a different reaction pathway, improving the acetaldehyde route by ethanol dehydrogenation, instead of the ethylene route by ethanol dehydration or methane re-adsorption, thus increasing the catalytic activity and selectivity into hydrogen.

Experimental and modelling studies on continuous synthesis and refining of biodiesel in a dedicated bench scale unit using centrifugal contactor separator technology

NARCIS (Netherlands)

Abduh, Muhammad Yusuf; Martinez, Alberto Fernandez; Kloekhorst, Arjan; Manurung, Robert; Heeres, Hero J.

Continuous synthesis and refining of biodiesel (FAME) using a laboratory scale bench scale unit was explored. The unit consists of three major parts: (i) a continuous centrifugal contactor separator (CCCS) to perform the reaction between sunflower oil and methanol; (ii) a washing unit for the crude

Pre elementary design of primary reformer for hydrogen plant coupled with HTGR type NPP

International Nuclear Information System (INIS)

Dedy Priambodo; Erlan Dewita; Sudi Ariyanto

2012-01-01

Hydrogen has a high potent for new energy, because of it availability. Steam reforming is a fully developed commercial technology and is the most economical method for production of hydrogen. Steam reforming uses an external source of hot gas to heat tubes in which a catalytic reaction takes place that converts steam and lighter hydrocarbons such as natural gas (methane) or refinery feedstock into hydrogen and carbon monoxide (syngas) at high temperature on primary reformer (800-900°C). Utilization of helium from HTGR as heating medium for primary reformer has consequence to type and shape of its reactor. The main goal of this paper is to determine type/shape and pre elementary design of chemical reactor for the cogeneration system of Hydrogen Plant and HTGR The primary reformer for this system is Fixed Bed Multitube reactor with specification tube: NPS 3,5 Sch 40 ST 40S, 0.281 in thickness, number of tube 849 pieces and ASTM HH 30 for tube material. Tube arrangement is 'triangular pitch' on shell Split-Ring Floating Head from Steel Alloy SA 301 Grade B equipted with 8 baffles. (author)

Large scale steam flow test: Pressure drop data and calculated pressure loss coefficients

International Nuclear Information System (INIS)

Meadows, J.B.; Spears, J.R.; Feder, A.R.; Moore, B.P.; Young, C.E.

1993-12-01

This report presents the result of large scale steam flow testing, 3 million to 7 million lbs/hr., conducted at approximate steam qualities of 25, 45, 70 and 100 percent (dry, saturated). It is concluded from the test data that reasonable estimates of piping component pressure loss coefficients for single phase flow in complex piping geometries can be calculated using available engineering literature. This includes the effects of nearby upstream and downstream components, compressibility, and internal obstructions, such as splitters, and ladder rungs on individual piping components. Despite expected uncertainties in the data resulting from the complexity of the piping geometry and two-phase flow, the test data support the conclusion that the predicted dry steam K-factors are accurate and provide useful insight into the effect of entrained liquid on the flow resistance. The K-factors calculated from the wet steam test data were compared to two-phase K-factors based on the Martinelli-Nelson pressure drop correlations. This comparison supports the concept of a two-phase multiplier for estimating the resistance of piping with liquid entrained into the flow. The test data in general appears to be reasonably consistent with the shape of a curve based on the Martinelli-Nelson correlation over the tested range of steam quality

A bench-scale biotreatability methodology to evaluate field bioremediation

International Nuclear Information System (INIS)

Saberiyan, A.G.; MacPherson, J.R. Jr.; Moore, R.; Pruess, A.J.; Andrilenas, J.S.

1995-01-01

A bench-scale biotreatability methodology was designed to assess field bioremediation of petroleum contaminated soil samples. This methodology was performed successfully on soil samples from more than 40 sites. The methodology is composed of two phases, characterization and experimentation. The first phase is physical, chemical, and biological characterization of the contaminated soil sample. This phase determines soil parameters, contaminant type, presence of indigenous contaminant-degrading bacteria, and bacterial population size. The second phase, experimentation, consists of a respirometry test to measure the growth of microbes indirectly (via generation of CO 2 ) and the consumption of their food source directly (via contaminant loss). Based on a Monod kinetic analysis, the half-life of a contaminant can be calculated. Abiotic losses are accounted for based on a control test. The contaminant molecular structure is used to generate a stoichiometric equation. The stoichiometric equation yields a theoretical ratio for mg of contaminant degraded per mg of CO 2 produced. Data collected from the respirometry test are compared to theoretical values to evaluate bioremediation feasibility

A comprehensive energy–exergy-based assessment and parametric study of a hydrogen production process using steam glycerol reforming

International Nuclear Information System (INIS)

Hajjaji, Noureddine; Chahbani, Amna; Khila, Zouhour

2014-01-01

Various assessment tools are applied to comprehensively investigate a glycerol-to-hydrogen production system. These tools investigate the chemical reactions, design and simulate the entire hydrogen production process, study the energetic and exergetic performances and perform parametric analyses (using intuitive and design of experiment-based methods). Investigating the chemical reaction of steam glycerol reforming reveals that the optimal conditions, determined based on maximizing the hydrogen production while minimizing the methane and carbon monoxide contents and coke formation, can be achieved at a reforming temperature and a water-to-glycerol feed ratio (WGFR) of 950 K and 9, respectively. The thermal and exergetic efficiencies of the resulting process are 66.6% and 59.9%, respectively. These findings are lower than those cited in the literature and relative to other reformates (methane, ethanol and methanol). The parametric investigation indicates that the performance of the process (energetic and exergetic) could be ensured by using an appropriate and judiciously selected combination of the reactor temperature and WGFR. Based on the parametric energetic and exergetic investigation, WGFR = 6 and T = 1100 K appear to be the most accurate parameters for the entire glycerol-to-hydrogen process. For this recommend configuration, the thermal and exergetic efficiencies are 78.1% and 66.1%, respectively. - Highlights: • Energy and exergy analysis are used to assess glycerol-to-hydrogen process. • Recommended conditions for glycerol-to-hydrogen process are WGFR = 6 and T = 1100 K. • For recommend conditions, thermal and exergetic efficiencies are 78.1% and 66.1%. • Energy and exergy consideration should be included by engineers and scientists

Ethanol steam reforming heated up by molten salt CSP : reactor assessment

NARCIS (Netherlands)

Falco, de M.; Gallucci, F.

2010-01-01

In this paper hydrogen production via reforming of ethanol has been studied in a novel hybrid plant consisting in a ethanol reformer and a concentrating solar power (CSP) plant using molten salt as heat carrier fluid. The heat needed for the reforming of ethanol has been supplied to the system by

Ethanol steam reforming heated up by molten salt CSP: Reactor assessment

NARCIS (Netherlands)

De Falco, Marcello; Gallucci, F.

2010-01-01

In this paper hydrogen production via reforming of ethanol has been studied in a novel hybrid plant consisting in a ethanol reformer and a concentrating solar power (CSP) plant using molten salt as heat carrier fluid. The heat needed for the reforming of ethanol has been supplied to the system by

Nickel catalysts for internal reforming in molten carbonate fuel cells

NARCIS (Netherlands)

Berger, R.J.; Berger, R.J.; Doesburg, E.B.M.; Doesburg, E.B.M.; van Ommen, J.G.; Ross, J.R.H.; Ross, J.R.H.

1996-01-01

Natural gas may be used instead of hydrogen as fuel for the molten carbonate fuel cell (MCFC) by steam reforming the natural gas inside the MCFC, using a nickel catalyst (internal reforming). The severe conditions inside the MCFC, however, require that the catalyst has a very high stability. In

Steady-State Simulation of Steam Reforming of INEEL Tank Farm Waste

International Nuclear Information System (INIS)

Nichols, T.T.; Taylor, D.D.; Wood, R.A.; Barnes, C.M. email toddn@inel.gov

2002-01-01

A steady-state model of the Sodium-Bearing Waste steam reforming process at the Idaho National Engineering and Environmental Laboratory has been performed using the commercial ASPEN Plus process simulator. The preliminary process configuration and its representation in ASPEN are described. As assessment of the capability of the model to mechanistically predict product stream compositions was made, and fidelity gaps and opportunities for model enhancement were identified, resulting in the following conclusions: (1) Appreciable benefit is derived from using an activity coefficient model for electrolyte solution thermodynamics rather than assuming ideality (unity assumed for all activity coefficients). The concentrations of fifteen percent of the species present in the primary output stream were changed by more than 50%, relative to Electrolyte NRTL, when ideality was assumed; (2) The current baseline model provides a good start for estimating mass balances and performing integrated process optimization because it contains several key species, uses a mechanistic electrolyte thermodynamic model, and is based on a reasonable process configuration; and (3) Appreciable improvement to model fidelity can be realized by expanding the species list and the list of chemical and phase transformations. A path forward is proposed focusing on the use of an improved electrolyte thermodynamic property method, addition of chemical and phase transformations for key species currently absent from the model, and the combination of RGibbs and Flash blocks to simulate simultaneous phase and chemical equilibria in the off-gas treatment train

Energy Analysis of Cascade Heating with High Back-Pressure Large-Scale Steam Turbine

Directory of Open Access Journals (Sweden)

Zhihua Ge

2018-01-01

Full Text Available To reduce the exergy loss that is caused by the high-grade extraction steam of traditional heating mode of combined heat and power (CHP generating unit, a high back-pressure cascade heating technology for two jointly constructed large-scale steam turbine power generating units is proposed. The Unit 1 makes full use of the exhaust steam heat from high back-pressure turbine, and the Unit 2 uses the original heating mode of extracting steam condensation, which significantly reduces the flow rate of high-grade extraction steam. The typical 2 × 350 MW supercritical CHP units in northern China were selected as object. The boundary conditions for heating were determined based on the actual climatic conditions and heating demands. A model to analyze the performance of the high back-pressure cascade heating supply units for off-design operating conditions was developed. The load distributions between high back-pressure exhaust steam direct supply and extraction steam heating supply were described under various conditions, based on which, the heating efficiency of the CHP units with the high back-pressure cascade heating system was analyzed. The design heating load and maximum heating supply load were determined as well. The results indicate that the average coal consumption rate during the heating season is 205.46 g/kWh for the design heating load after the retrofit, which is about 51.99 g/kWh lower than that of the traditional heating mode. The coal consumption rate of 199.07 g/kWh can be achieved for the maximum heating load. Significant energy saving and CO2 emission reduction are obtained.

Utilization of acetone-butanol-ethanol-water mixture obtained from biomass fermentation as renewable feedstock for hydrogen production via steam reforming: Thermodynamic and energy analyses.

Science.gov (United States)

Kumar, Brajesh; Kumar, Shashi; Sinha, Shishir; Kumar, Surendra

2018-08-01

A thermodynamic equilibrium analysis on steam reforming process to utilize acetone-butanol-ethanol-water mixture obtained from biomass fermentation as biorenewable fuel has been performed to produce clean energy carrier H 2 via non-stoichiometric approach namely Gibbs free energy minimization method. The effect of process variables such as temperature (573-1473 K), pressure (1-10 atm), and steam/fuel molar feed ratio (F ABE  = 5.5-12) have been investigated on equilibrium compositions of products, H 2 , CO, CO 2 , CH 4 and solid carbon. The best suitable conditions for maximization of desired product H 2 , suppression of CH 4 , and inhibition of solid carbon are 973 K, 1 atm, steam/fuel molar feed ratio = 12. Under these conditions, the maximum molar production of hydrogen is 8.35 with negligible formation of carbon and methane. Furthermore, the energy requirement per mol of H 2 (48.96 kJ), thermal efficiency (69.13%), exergy efficiency (55.09%), exergy destruction (85.36 kJ/mol), and generated entropy (0.29 kJ/mol.K) have been achieved at same operating conditions. Copyright © 2018 Elsevier Ltd. All rights reserved.

Thermal Modeling and Management of Solid Oxide Fuel Cells Operating with Internally Reformed Methane

Science.gov (United States)

Wu, Yiyang; Shi, Yixiang; Cai, Ningsheng; Ni, Meng

2018-06-01

A detailed three-dimensional mechanistic model of a large-scale solid oxide fuel cell (SOFC) unit running on partially pre-reformed methane is developed. The model considers the coupling effects of chemical and electrochemical reactions, mass transport, momentum and heat transfer in the SOFC unit. After model validation, parametric simulations are conducted to investigate how the methane pre-reforming ratio affects the transport and electrochemistry of the SOFC unit. It is found that the methane steam reforming reaction has a "smoothing effect", which can achieve more uniform distributions of gas compositions, current density and temperature among the cell plane. In the case of 1500 W/m2 power density output, adding 20% methane absorbs 50% of internal heat production inside the cell, reduces the maximum temperature difference inside the cell from 70 K to 22 K and reduces the cathode air supply by 75%, compared to the condition of completely pre-reforming of methane. Under specific operating conditions, the pre-reforming ratio of methane has an optimal range for obtaining a good temperature distribution and good cell performance.

A novel approach to the experimental study on methane/steam reforming kinetics using the Orthogonal Least Squares method

Science.gov (United States)

Sciazko, Anna; Komatsu, Yosuke; Brus, Grzegorz; Kimijima, Shinji; Szmyd, Janusz S.

2014-09-01

For a mathematical model based on the result of physical measurements, it becomes possible to determine their influence on the final solution and its accuracy. However, in classical approaches, the influence of different model simplifications on the reliability of the obtained results are usually not comprehensively discussed. This paper presents a novel approach to the study of methane/steam reforming kinetics based on an advanced methodology called the Orthogonal Least Squares method. The kinetics of the reforming process published earlier are divergent among themselves. To obtain the most probable values of kinetic parameters and enable direct and objective model verification, an appropriate calculation procedure needs to be proposed. The applied Generalized Least Squares (GLS) method includes all the experimental results into the mathematical model which becomes internally contradicted, as the number of equations is greater than number of unknown variables. The GLS method is adopted to select the most probable values of results and simultaneously determine the uncertainty coupled with all the variables in the system. In this paper, the evaluation of the reaction rate after the pre-determination of the reaction rate, which was made by preliminary calculation based on the obtained experimental results over a Nickel/Yttria-stabilized Zirconia catalyst, was performed.

Hydrogen Production from Ethanol Steam Reforming over SnO2-K2O/Zeolite Y Catalyst

International Nuclear Information System (INIS)