go to top scroll for more

Joint UK / China Hydrogen production network

Reference Number
EP/G062374/1
Title
Joint UK / China Hydrogen production network
Status
Completed
Energy Categories
Fossil Fuels: Oil Gas and Coal(Coal, Coal conversion (excluding IGCC))
Hydrogen and Fuel Cells(Hydrogen, Hydrogen production)
Research Types
Basic and strategic applied research
Science and Technology Fields
ENGINEERING AND TECHNOLOGY (Chemical Engineering)
UKERC Cross Cutting Characterisation
Not Cross-cutting
Principal Investigator
Professor VN Sharifi
Chemical and Process Engineering
University of Sheffield
Award Type
Standard
Funding Source
EPSRC
Start Date
01 October 2009
End Date
30 September 2012
Duration
36 months
Total Grant Value
£177,648
Industrial Sectors
Energy
Region
Yorkshire & Humberside
Programme
Energy : Energy
Investigators
Principal Investigator
Professor VN Sharifi, Chemical and Process Engineering, University of Sheffield
Other Investigator
Professor J Swithenbank, Chemical and Process Engineering, University of Sheffield
Industrial Collaborator
Project Contact, Research Partner in China
Web Site
Objectives
Note : these 4 grants are linked EP/G06265X/1, EP/G06279X/1, EP/G062374/1, EP/G063265/1
Abstract
The increasing threat posed by enhanced global warming, together with the requirement to secure energy supplies for both countries have led to this proposal for a collaboration of experts between China and the U.K. in clean technologies for energy production from fossil fuels. The overarching theme of the proposal is the production of clean energy/H2 from coal, via a number of thermochemical routes with the CO2 separated and ready for sequestration. We will investigate two forms of advanced chemical cycles which allow clean hydrogen to be produced from fossil fuels, without (unlike with current technology) a large energy penalty associated with capturing the CO2. These processes are at an early stage of development with research required on the underlying science of the concepts, as wellas how these processes can be scaled up from the laboratory. Both types of chemical cycle make use of solid reactants which either act as CO2 acceptors or oxygen carriers.1. Advanced gasificationprocesses using the calcination-carbonation cycle: The original "ZECA" process aimed to generate hydrogen from coal, by first hydrogasifying the coal to methane, then reforming to syngas, before shiftingto H2. The shift reaction was to be performed using calcium oxide to remove the CO2 and move the equilibrium of the water-gas shift reaction over to H2. The need to first reform the methane in to syngas faced potential problems with the sulphur in the coal which will contaminate the methane as H2S, and deactivate reforming catalysts. Here we will investigate combining the reformer and shift reactors, and the effect of H2S on the calcium looping agent, which must be repeatedly cycled between CaO and CaCO3. The hydrogasification of a spectrum of fuels needs to be explored, since the efficiency of this process will depend on the ability to completely convert the solid fuel into methane. At a pilot scale the continuous operation of enhanced water-gas shift process will be investigated, in acirculating fluidised bed.2. Hydrogen production using the iron-oxide based redox cycle: In chemical looping combustion, a fuel can be burned with a metal oxide (rather than air) to produce a stream of pure CO2. For power generation, the reduced oxide can be reoxidised with air to release heat. Some metals and oxides (e.g. iron) can be partially oxidised with steam to produce very pure H2.Fe2O3oxide can be reduced to FeO or Fe using syngas; Fe and FeO can then be oxidised with steam giving Fe3O4 and hydrogen. The cycle can be completed by oxidising the Fe3O4 with air.Here we will investigate the continuous operation of this process on a laboratory scale, and on a pilot scale, using a combination of fluidised and moving bed reactors. The syngas must be generated from coal and willcontain tars and H2S. We will investigate the affect of volatile material and sulphur on the iron based carrier, i.e. the extent to which the metal oxides can combust the volatiles, and whether the oxides are deactivated by sulphur. The use of these metal oxides ad tar cracking catalysts during gasification will also be investigated.Both the calcium based CO2 acceptors and the metal oxide based oxygen carriers must undergo many cycles of operation. Natural materials will often rapidly degrade. Artificial particles can be produced which have better characteristics. However, the behaviour of the particles is a very strong function of the physical structure, and the presence of additives/contaminants. We will investigate how the formulation of these materials affects their physical structures and the impact this will have on the reactivity over many cycles
Data

No related datasets

Projects

No related projects

Publications

No related publications

Added to Database
02/09/09