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Nuclear Production of Hydrogen, Fourth Information Exchange ...

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EXECUTIVE SUMMARY<br />

iodine concentration. The experimental data suggest that existing models overestimate iodine vapour<br />

concentration at low pressures, but underestimate it at higher pressures. HI and H 2 O concentrations<br />

match current models fairly well at low iodine pressures. <strong>Hydrogen</strong> formation at higher pressures<br />

must be accounted for while using these techniques. CEA will use the new data to construct a new<br />

thermodynamic model for the S-I cycle.<br />

Dr. Max Gorensek <strong>of</strong> SRNL presented on the efficiency <strong>of</strong> a recuperative bayonet decomposition<br />

reactor for the thermochemical sulphur cycle. SRNL conducted a study to analyse heat transfer<br />

characteristics <strong>of</strong> a bayonet-style decomposer for the sulphuric acid decomposition section. A pinch<br />

analysis <strong>of</strong> the reactor was completed, and a statistical design <strong>of</strong> experiments was presented.<br />

A temperature-enthalpy curve for the reactor was generated for the pinch analysis. Statistical methods<br />

were then used to determine operating windows and conditions for minimum heat requirements.<br />

A heuristic approach was adopted after surface response and neural network modelling techniques<br />

failed. High temperatures, low pressures and high sulphuric acid feed concentrations led to the best<br />

results. Reactor operating temperature may be lowered to 825°C to alleviate materials concerns, but<br />

the potential efficiency advantage <strong>of</strong> sulphur cycle over direct electrolysis is impacted. Dropping the<br />

reactor outlet temperature below 825°C does not lead to an efficient process.<br />

Dr. Kikwang Bae <strong>of</strong> KIER presented on the development status <strong>of</strong> the HIx decomposition process<br />

in Korea. The paper examined the advantages and disadvantages <strong>of</strong> the S-I cycle, and described the<br />

programme at KIER for development <strong>of</strong> the process. KIER is implementing electro-electro dialysis (EED)<br />

for production <strong>of</strong> super-azeotropic HI in water. Initial experimental results showed stable hydrogen<br />

production for a period <strong>of</strong> five hours. An earlier version <strong>of</strong> an experimental device to demonstrate the<br />

process in glass is being upgraded to increase safety and durability. Current membrane technology<br />

does not allow for efficient use <strong>of</strong> EED alone, but KIER is studying the concept <strong>of</strong> combining EED with<br />

reactive distillation. Cycle efficiency as a function <strong>of</strong> EED cell potential was presented, along with<br />

results <strong>of</strong> experiments designed to optimise conditions in the Bunsen reaction section. KIER intends to<br />

build a device similar to the SNL-CEA-GA demonstration apparatus and operate it starting in 2011.<br />

It will be designed for a 200 litre per hour output <strong>of</strong> hydrogen.<br />

Dr. Frikkie van Niekerk <strong>of</strong> North-West University, South Africa, presented on the situation <strong>of</strong><br />

South Africa. Global and South African energy concerns were outlined, followed by PBMR and SASOL<br />

strategies to address these concerns. South Africa ranks 12 th in the world for CO 2 emissions per capita.<br />

From 2006, demand for power was greater than the domestic supply. <strong>Nuclear</strong> power is expected to<br />

supply 30% <strong>of</strong> energy needs by 2030 (currently 6%). A business plan for hydrogen production was<br />

reviewed, as was a down-select process for determining a thermochemical cycle for implementation.<br />

The S-I cycle, hybrid sulphur and high-temperature electrolysis were considered, with hybrid sulphur<br />

being selected. Current efforts are under way to resolve the remaining technical challenges with<br />

electrolysers. Preliminary work on a plasma-arc process for conversion <strong>of</strong> CH 4 to syngas was<br />

presented, with comparisons to standard SMR. Finally, steps to finalise and implement the hydrogen<br />

business plan were discussed.<br />

Dr. Anne Saturnin <strong>of</strong> CEA presented on behalf <strong>of</strong> Dr. Jean Leybros <strong>of</strong> CEA about the ILS experiment<br />

for the hybrid sulphur cycle at CEA Marcoule. The paper described the CEA programme to develop the<br />

hybrid sulphur process. CEA has operated a pilot device since April 2008. To reduce sulphur build-up<br />

on the cathode, CEA is developing new membranes with reduced SO 2 transport characteristics and<br />

good ionic conductivity. To reduce cell voltages, CEA is testing higher activity anodic catalysts and<br />

also porous anodes. A flow sheet has been developed with 42% thermodynamic efficiency. Capital<br />

costs for a 1 000 mole H 2 /sec plant are estimated at just over EUR 1 billion. Sensitivity studies were<br />

conducted to determine major cost drivers for the process. Future efforts will include continued<br />

experimental work, in addition to improved simulations <strong>of</strong> the electrochemical portions <strong>of</strong> the flow<br />

sheet. This integrated approach will assist in analysing the potential <strong>of</strong> the hybrid sulphur process in<br />

comparison with other thermochemical cycles.<br />

Dr. William Summers <strong>of</strong> SRNL presented on the development status <strong>of</strong> the hybrid sulphur cycle.<br />

SRNL is studying the hybrid sulphur process. They are developing a PEM-based electrolyser design.<br />

This leverages fuel cell technology. Stated advantages are smaller footprint, decreased cell potential,<br />

simpler hydrogen recovery and lower capital cost. Experimentally, progress has been made in<br />

identifying key membrane and catalyst characteristics for the electrolyser. Pt and Pt alloy catalysts<br />

exhibit excellent performance for the oxidation <strong>of</strong> SO 2 oxidation. Oxidation kinetics is the largest<br />

contributor to overpotential losses. Single and multi-cell stacks have been operated, and reduction <strong>of</strong><br />

12 NUCLEAR PRODUCTION OF HYDROGEN – © OECD/NEA 2010

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