Production & Supply Chain

While the effects of ongoing cost reductions in renewables batteries and electrolyzers on future energy systems have been extensively investigated the effects of significant advances in CO2 capture and storage (CCS) technologies have received much less attention. This research gap is addressed via a long-term (2050) energy system model loosely based on Germany yielding four main findings. First CCS-enabled pathways offer the greatest benefits in the hydrogen sector where hydrogen prices can be reduced by two-thirds relative to a scenario without CCS. Second advanced blue hydrogen technologies can reduce total system costs by 12% and enable negative CO2 emissions due to higher efficiencies and CO2 capture ratios. Third co-gasification of coal and biomass emerged as an important enabler of these promising results allowing efficient exploitation of limited biomass resources to achieve negative emissions and limit the dependence on imported natural gas. Finally CCS decarbonization pathways can practically and economically incorporate substantial shares of renewable energy to reduce fossil fuel dependence. Such diversification of primary energy inputs increases system resilience to the broad range of socio-techno-economic challenges facing the energy transition. In conclusion balanced blue-green pathways offer many benefits and deserve serious consideration in the global decarbonization effort.

Variable low-cost low-carbon electricity that would otherwise be curtailed may provide a substantial economic opportunity for entities that can flexibly adapt their electricity consumption. We used historical hourly weather data over the contiguous U.S. to model the characteristics of least-cost electricity systems dominated by variable renewable generation that powered firm and flexible electricity demands (loads). Scenarios evaluated included variable wind and solar power battery storage and dispatchable natural gas with carbon capture and storage with electrolytic hydrogen representing a prototypical flexible load. When flexible loads were small excess generation capacity was available during most hours allowing flexible loads to operate at high capacity factors. Expanding the flexible loads allowed the least-cost systems to more fully utilize the generation capacity built to supply firm loads and thus reduced the average cost of delivered electricity. The macro-scale energy model indicated that variable renewable electricity systems optimized to supply firm loads at current costs could supply 25% or more additional flexible load with minimal capacity expansion while resulting in reduced average electricity costs (10% or less capacity expansion and 10% to 20% reduction in costs in our modeled scenarios). These results indicate that adding flexible loads to electricity systems will likely allow more full utilization of generation assets across a wide range of system architectures thus providing new energy services with infrastructure that is already needed to supply firm electricity loads.

In this paper a simplified model of a Polymer Electrolyte Membrane (PEM) water electrolysis cell is presented and compared with experimental data at 60 ◦C and 80 ◦C. The model utilizes the same modelling approach used in previous work where the electrolyzer cell is divided in four subsections: cathode anode membrane and voltage. The model of the electrodes includes key electrochemical reactions and gas transport mechanism (i.e. H2 O2 and H2O) whereas the model of the membrane includes physical mechanisms such as water diffusion electro osmotic drag and hydraulic pressure. Voltage was modelled including main overpotentials (i.e. activation ohmic concentration). First and second law efficiencies were defined. Key empirical parameters depending on temperature were identified in the activation and ohmic overpotentials. The electrodes reference exchange current densities and change transfer coefficients were related to activation overpotentials whereas hydrogen ion diffusion to Ohmic overvoltages. These model parameters were empirically fitted so that polarization curve obtained by the model predicted well the voltage at different current found by the experimental results. Finally from the efficiency calculation it was shown that at low current densities the electrolyzer cell absorbs heat from the surroundings. The model is not able to describe the transients involved during the cell electrochemical reactions however these processes are assumed relatively fast. For this reason the model can be implemented in system dynamic modelling for hydrogen production and storage where components dynamic is generally slower compared to the cell electrochemical reactions dynamics.

The continuous rise of global carbon emissions demands the utilization of fossil fuels in a sustainable way. Owing to various forms of emissions our environment conditions might be affected necessitating more focus of scientists and researchers to upgrade oil processing to more efficient manner. Gasification is a potential technology that can convert fossil fuels to produce clean and environmentally friendly hydrogen fuel in an economical manner. Therefore this study analyzed and examined it critically. In this study two different routes for the production of high-purity hydrogen from vacuum residue while minimizing the carbon emissions were proposed. The first route (Case I) studied the gasification of heavy vacuum residue (VR) in series with dry methane reforming (DMR). The second route studied the gasification of VR in parallel integration with DMR (Case II). After investigating both processes a brief comparison was made between the two routes of hydrogen production in terms of their CO2 emissions energy efficiency energy consumption and environmental and economic impacts. In this study the two vacuum-residue-to-hydrogen (VRTH) processes were simulated using Aspen Plus for a hydrogen production capacity of 50 t/h with 99.9 wt.% purity. The results showed that Case II offered a process energy efficiency of 57.8% which was slightly higher than that of Case I. The unit cost of the hydrogen product for Case II was USD 15.95 per metric ton of hydrogen which was almost 9% lower than that of Case I. In terms of the environmental analysis both cases had comparably low carbon emissions of around 8.3 kg of CO2/kg of hydrogen produced; with such high purity the hydrogen could be used for production of other products further downstream or for industrial applications.

The natural gas (NG) reforming is currently one of the low-cost methods for hydrogen production. However the mixture of H2 and CO2 in the produced gas inevitably includes CO2 and necessitates the costly CO2 separation. In this work a novel double chemical looping involving both combustion (CLC) and sorption-enhanced reforming (SE-CLR) was proposed towards the co-production of H2 and CO (CLC-SECLRHC) in two separated streams. CLC provides reactant CO2 and energy to feed SECLRHC which generates hydrogen in a higher purity as well as the calcium cycle to generate CO in a higher purity. Techno-economic assessment of the proposed system was conducted to evaluate its efficiency and economic competitiveness. Studies revealed that the optimal molar ratios of oxygen carrier (OC)/NG and steam/NG for reforming were recommended to be 1.7 and 1.0 respectively. The heat integration within CLC and SECLRHC units can be achieved by circulating hot OCs. The desired temperatures of fuel reactor (FR) and reforming reactor (RR) should be 850 °C and 600 °C respectively. The heat coupling between CLC and SECLRHC units can be realized via a jacket-type reactor and the NG split ratio for reforming and combustion was 0.53:0.47. Under the optimal conditions the H2 purity the H2 yield and the CH4 conversion efficiency were 98.76% 2.31 mol mol-1 and 97.96% respectively. The carbon and hydrogen utilization efficiency respectively were 58.60% and 72.45% in terms of the total hydrogen in both steam and NG. The exergy efficiency of the overall process reached 70.28%. In terms of the conventional plant capacity (75×103 t y-1 ) and current raw materials price (2500 $ t-1 ) the payback period can be 6.2 years and the IRR would be 11.5 demonstrating an economically feasible and risk resistant capability.

Hydrogen is increasingly being viewed as a significant fuel for future industrial processes as it offers pathways to zero emission. The UK sees hydrogen as one of a handful of low-carbon solutions for transition to net zero. Currently most hydrogen production is from steam reforming of natural gas or coal gasification both of which involve the release of carbon dioxide. Hydrogen production from mini decentralised grids via a thermochemical process coupled with electricity production could offer favourable economics for small modular reactors (SMRs) whereby demand or grid management as a solution would include redirecting the power for hydrogen production when electricity demand is low. It also offers a clean-energy alternative to the aforementioned means. SMRs could offer favourable economics due to their flexible power system as part of the dual-output function. This study objective is to investigate the critical performance parameters associated with the nuclear power plant (NPP) the cycle working fluids and control-system design for switching between electricity and hydrogen demand to support delivery as part of a mini grid system for a reactor power delivering up to approximately 600 MWth power. The novelty of the work is in the holistic parametric analysis undertaken using a novel in-house tool which analyses the NPP using different working fluids with a control function bolt-on at the offtake for hydrogen production. The results indicate that the flow conditions at the offtake can be maintained. The choice of working fluids affects the pressure component. However the recuperator and heat-exchanger effectiveness are considered as efficiency-limiting factors for hydrogen production and electricity generation. As such the benefit of high-technology heat exchangers cannot be underestimated. This is also true when deciding on the thermochemical process to bolt onto the plant. The temperature of the gas at the end of the pipeline should also be considered to ensure that the minimum temperature-requirement status for hydrogen production is me

On this episode of EAH we are joined by Andrew Clennett Co-Founder and CEO of Hiringa Energy. Hiringa is headquartered in New Zealand where they are building clean hydrogen production projects using renewable energy to displace the use of fossil fuels for transport and industrial feedstock across New Zealand. We are delighted to have Andrew with us today to speak about how Hiringa are using hydrogen to change the energy and carbon landscape of New Zealand.

This podcast can be found on their website

Turquoise hydrogen is produced from methane cracking a cleaner alternative to steam methane reforming. This study looks at two proposed systems based on solar methane cracking for low-carbon fuel production. The systems utilize different pathways to convert the hydrogen into a suitable form for transportation and utilize the carbon solid by-product. A direct carbon fuel cell is integrated to utilize the carbon and capture the CO2 emissions. The CO2 generated is utilized for fuel production using CO2 hydrogenation or co-electrolysis. An advanced exergetic analysis is conducted on these systems using Aspen plus simulations of the process. The exergetic efficiency waste exergy ratio exergy destruction ratio exergy recoverability ratio environmental effect factor and the exergetic sustainability index were determined for each system and the subsystems. Solar methane cracking was found to have an environmental effect factor of 0.08 and an exergetic sustainability index of 12.27.

Presently hydrogen is for ~50% produced by steam reforming of natural gas – a process leading to significant emissions of greenhouse gas (GHG). About 30% is produced from oil/naphtha reforming and from refinery/chemical industry off-gases. The remaining capacity is covered for 18% from coal gasification 3.9% from water electrolysis and 0.1% from other sources. In the foreseen future hydrogen economy green hydrogen production methods will need to supply hydrogen to be used directly as fuel or to generate synthetic fuels to produce ammonia and other fertilizers (viz. urea) to upgrade heavy oils (like oil sands) and to produce other chemicals. There are several ways to produce H2 each with limitations and potential such as steam reforming electrolysis thermal and thermo-chemical water splitting dark and photonic fermentation; gasification and catalytic decomposition of methanol. The paper reviews the fundamentals and potential of these alternative process routes. Both thermo-chemical water splitting and fermentation are marked as having a long term but high "green" potential.

Green hydrogen production i.e. produced on a CO2 -neutral basis through the electrolysis of water employing renewable electricity has attracted increasing attention. The electricity required is generated from Renewable Energy Sources (RES) for example wind energy hydropower or solar energy. Since neither the process of production nor the end products of H2 and O2 are harmful to the environment green hydrogen is climate neutral. Developing electrolysis technology is therefore a research topic to follow. Anion Exchange Membrane (AEM) Water Electrolysis (WE) is an innovative technology that couples the advantages of the more mature technologies of Proton Exchange Membrane (PEM) and conventional alkaline electrolysis with the potential to eliminate the drawbacks of both. AEMWE technology is in an evolutionary stage and involves more investigation on several research topics such as membrane and catalyst development and stability as well as alternative feeding solutions that do not compromise the availability of fresh water. These topics are addressed in this paper mentioning the state-of-the-art materials new promising ones and providing future research directions to improve AEMWE towards a most mature technology.