Canada

This paper examines the helium dispersion behaviour in a 16.6 m3 enclosure with a small opening in the floor and distributed leaks along the edges. Helium a simulant for hydrogen was injected near the center of the floor with an injection rate ranging from 2 to 50 standard liters per minute (Richardson number of 0.3–134) through an upward-facing nozzle. In a short-term transient the helium distribution predicted with the models of Baines & Turner (1969) and Worster & Huppert (1983) matched the measured distributions reasonably well. In a long-term transient the vertical helium profile always reached a steady state which consisted of a homogenous layer at the top overlaying a stratified layer at the bottom. The helium transients in the uniform layer predicted with the models of Lowesmith (2009) and Prasad & Yang (2010) assuming a vent was located in the ceiling were in good agreement with the measured transients.

For more than a century our nation’s brightest minds have been working on the technology to turn the invisible promise of hydrogen into tangible solutions. Canadian ingenuity and innovation has once again brought us to a pivotal moment. As we rebuild our economy from the impacts of COVID-19 and fight the existential threat of climate change the development of low-carbon hydrogen is a strategic priority for Canada. The time to act is now.<br/>The Hydrogen Strategy for Canada lays out an ambitious framework for actions that will cement hydrogen as a tool to achieve our goal of net-zero emissions by 2050 and position Canada as a global industrial leader of clean renewable fuels. This strategy shows us that by 2050 clean hydrogen can help us achieve our net-zero goal—all while creating jobs growing our economy and protecting our environment. This will involve switching from conventional gasoline diesel and natural gas to zero-emissions fuel sources taking advantage of new regulatory environments and embracing new technologies to give Canadians more choice of zero emission alternatives.<br/>As one of the top 10 hydrogen producers in the world today we are rich in the feedstocks that produce hydrogen. We are blessed with a strong energy sector and the geographic assets that will propel Canada to be a major exporter of hydrogen and hydrogen technologies. Hydrogen might be nature’s smallest molecule but its potential is enormous. It provides new markets for our conventional energy resources and holds the potential to decarbonize many sectors of our economy including resource extraction freight transportation power generation manufacturing and the production of steel and cement. This Strategy is a call to action. It will spur investments and strategic partnerships across the country and beyond our borders. It will position Canada to seize economic and environmental opportunities that exist coast to coast. Expanding our exports. Creating as many as 350000 good green jobs over the next three decades. All while dramatically reducing our greenhouse gas emissions. And putting a net-zero future within our reach.<br/>The importance of Canada’s resource industries and our clean technology sectors has been magnified during the pandemic. We must harness our combined will expertise and financial resources to fully seize the opportunities that hydrogen presents. This strategy is the product of three years of study and analysis including extensive engagement sessions where we heard from more than 1500 of our country’s leading experts and stakeholders. But its release is not the end of a process. This is only the beginning. Together we will use this Strategy to guide our actions and investments. By working with provinces and territories Indigenous partners and the private-sector and by leveraging our many advantages we will create the prosperity we all want protect the planet we all cherish and we will ensure we leave no one behind.

A new spinelized Ni catalyst (Ni-UGSO) using Ni(NO₃)₂·6H₂O as the Ni precursor was prepared according to a less material intensive protocol. The support of this catalyst is a negative-value mining residue UpGraded Slag Oxide (UGSO) produced from a TiO2 slag production unit. Applied to dry reforming of methane (DRM) at atmospheric pressure T = 810 °C space velocity of 3400 mL/(h·g) and molar CO₂/CH₄ = 1.2 Ni-UGSO gives a stable over 168 h time-on-stream methane conversion of 92%. In this DRM reaction optimization study: (1) the best performance is obtained with the 10–13 wt% Ni load; (2) the Ni-UGSO catalysts obtained from two different batches of UGSO demonstrated equivalent performances despite their slight differences in composition; (3) the sulfur-poisoning resistance study shows that at up to 5.5 ppm no Ni-UGSO deactivation is observed. In steam reforming of methane (SRM) Ni-UGSO was tested at 900 °C and a molar ratio of H₂O/CH₄ = 1.7. In this experimental range CH4 conversion rapidly reached 98% and remained stable over 168 h time-on-stream (TOS). The same stability is observed for H₂ and CO yields at around 92% and 91% respectively while H₂/CO was close to 3. In mixed (dry and steam) methane reforming using a ratio of H₂O/CH₄ = 0.15 and CO2/CH4 = 0.97 for 74 h and three reaction temperature levels (828 °C 847 °C and 896 °C) CH₄ conversion remains stable; 80% at 828 °C (26 h) 85% at 847 °C (24 h) and 95% at 896 °C (24 h). All gaseous streams have been analyzed by gas chromatography. Both fresh and used catalysts are analyzed by scanning electron microscopy-electron dispersive X-ray spectroscopy (SEM-EDXS) X-ray diffraction (XRD) and thermogravimetric analysis (TGA) coupled with mass spectroscopy (MS) and BET Specific surface. In the reducing environment of reforming such catalytic activity is mainly attributed to (a) alloys such as FeNi FeNi3 and Fe3Ni2 (reduction of NiFe2O4 FeNiAlO4) and (b) to the solid solution NiO-MgO. The latter is characterized by a molecular distribution of the catalytically active Ni phase while offering an environment that prevents C deposition due to its alkalinity.

To reduce greenhouse gas emissions from natural gas use utilities are investigating the potential of adding hydrogen to their distribution grids. This will reduce the carbon dioxide emissions from grid-connected engines used for stationary power generation and it may also impact their power output and efficiency. Promisingly hydrogen and natural gas mixtures have shown encouraging results regarding engine power output pollutant emissions and thermal efficiency in well-controlled on-road vehicle applications. This work investigates the effects of adding hydrogen to the natural gas fuel for a lean-burn spark-ignited four-stroke 8.9 liter eight-cylinder naturally aspirated engine used in a commercial stationary power generation application via an engine model developed in the GT-SUITETM modelling environment. The model was validated for fuel consumption air flow and exhaust temperature at two operating modes. The focus of the work was to assess the sensitivity of the engine’s power output brake thermal efficiency and pollutant emissions to blends of methane with 0–30% (by volume) hydrogen. Without adjusting for the change in fuel energy the engine power output dropped by approximately 23% when methane was mixed with 30% by volume hydrogen. It was found that increasing the fueling rate to maintain a constant equivalence ratio prevented this drop in power and reduced carbon dioxide emissions by almost 4.5%. In addition optimizing the spark timing could partially offset the increases in in-cylinder burned and unburned gas temperatures and in-cylinder pressures that resulted from the faster combustion rates when hydrogen was added to the natural gas. Understanding the effect of fuel change in existing systems can provide insight on utilizing hydrogen and natural gas mixtures as the primary fuel without the need for major changes in the engine.

Hydrogen as a clean zero-emission energy fuel will play a critical role in energy transition and achievement of the net-zero target in 2050. Hydrogen delivery is integral to the entire value chain of a full-scale hydrogen economy. This work conducted a systematic review and analysis of various hydrogen transportation methods including truck tankers for liquid hydrogen tube trailers for gaseous hydrogen and pipelines by identifying and ranking the main properties and affecting factors associated with each method. It is found that pipelines especially the existing natural gas pipelines provide a more efficient and cheaper means to transport hydrogen over long distances. Analysis was further conducted on Canadian natural gas pipeline network which has been operating for safe effective and efficient energy transport over six decades. The established infrastructure along with the developed operating and management experiences and skillful manpower makes the existing pipelines the best option for transport of hydrogen in either blended or pure form in the country. The technical challenges in repurposing the existing natural gas pipelines for hydrogen service were discussed and further work was analyzed.

Aerospace parts made of high strength steels such as landing gears and helicopter transmissions are often electroplated to satisfy various engineering specifications. However plated parts are occasionnaly rejected because of hydrogen embrittlement and the industry has few means of evaluating quantitatively the actual damage caused by hydrogen. In the present article we developed a novel method to measure the stress intensity threshold for hydrogen embrittlement (Kth) in industrial plating conditions. The method consists in plating side-grooved CT samples in industrial plating baths and measuring Kth with an incremental step loading methodology. We validated the method with a benchmark case known to produce embrittlement (omitted post-plating bake) and we used the method on a test case for which the level of embrittlement was unknown (delayed bake). For the benchmark case we measured a Kth of 49.0 MPa m0.5 for non-baked samples. This value is significantly lower than the fracture toughness of the unplated material which is 63.8 MPa m0.5 . We conclude that this novel combination of geometry and test method is efficient in quantifying hydrogen embrittlement of samples plated in industrial conditions. For the test case the Kth are respectively 57.9 MPa m0.5 and 58.8 MPa m0.5 for samples baked 100 h and 4 h after plating. We conclude that delaying the post-plating bake does not cause hydrogen embrittlement in the studied conditions. Using a finite element hydrogen diffusion analysis we argue that the side grooves on CT samples increase the sensitivity to hydrogen embrittlement in comparison to smooth samples. In smooth samples a zone of plane stress at the surface of the specimen shields hydrogen from penetrating to the center of the specimen a phenomenon which is alleviated with machining side grooves.

This paper compares six (6) alternatives for green hydrogen transport at sea. Two (2) alternatives of liquid hydrogen (LH2) by ship two (2) alternatives of compressed hydrogen (cH2) by ship and two (2) alternatives of hydrogen by pipeline. The ship alternatives study having hydrogen storage media at both end terminals to reduce the ships’ time at port or prescinding of them and reduce the immobilized capital. In the case of the pipeline new models are proposed by considering pressure costs. One scenario considers that there are compression stations every 500 km and the other one considers that there are none along the way. These alternatives are assessed under nine different scenarios that combine three distances: 100 km 2500 km and 5000 km; and three export rates of hydrogen 100 kt/y 1 Mt/y and 10 Mt/y. The results show including uncertainty bands that for the 100 km of distance the best alternative is the pipeline. For 2500 km and 100 kt/y the top alternative is cH2 shipping without storage facilities at the port terminals. For 2500 km and 1 Mt/y and for 5000 km and 100 kt/y the best alternatives are cH2 or LH2 shipping. For the remaining scenarios the best alternative is LH2 shipping.

Mg-based materials are one of the most promising hydrogen storage candidates due to their high hydrogen storage capacity environmental benignity and high Clarke number characteristics. However the limited thermodynamics and kinetic properties pose major challenges for their engineering applications. Herein we review the recent progress in improving their thermodynamics and kinetics with an emphasis on the models and the influence of various parameters in the calculated models. Subsequently the impact of alloying composite and nano-crystallization on both thermodynamics and dynamics are discussed in detail. In particular the correlation between various modification strategies and the hydrogen capacity dehydrogenation enthalpy and temperature hydriding/dehydriding rates are summarized. In addition the mechanism of hydrogen storage processes of Mg-based materials is discussed from the aspect of classical kinetic theories and microscope hydrogen transferring behavior. This review concludes with an outlook on the remaining challenge issues and prospects.

Interest in hydrogen as an energy carrier is growing as countries look to reduce greenhouse gas (GHG) emissions in hard-to-abate sectors. Previous works have focused on hydrogen production well-to-wheel analysis of fuel cell vehicles and vehicle refuelling costs and emissions. These studies use high-level estimates for the hydrogen transportation systems that lack sufficient granularity for techno-economic and GHG emissions analysis. In this work we assess and compare the unit costs and emission footprints (direct and indirect) of 32 systems for hydrogen transportation. Process-based models were used to examine the transportation of pure hydrogen (hydrogen pipeline and truck transport of gaseous and liquified hydrogen) hydrogen-natural gas blends (pipeline) ammonia (pipeline) and liquid organic hydrogen carriers (pipeline and rail). We used sensitivity and uncertainty analyses to determine the parameters impacting the cost and emission estimates. At 1000 km the pure hydrogen pipelines have a levelized cost of $0.66/kg H2 and a GHG footprint of 595 gCO2eq/kg H2. At 1000 km ammonia liquid organic hydrogen carrier and truck transport scenarios are more than twice as expensive as pure hydrogen pipeline and hythane and more than 1.5 times as expensive at 3000 km. The GHG emission footprints of pure hydrogen pipeline transport and ammonia transport are comparable whereas all other transport systems are more than twice as high. These results may be informative for government agencies developing policies around clean hydrogen internationally.

This study proposes a multi-level model predictive control (MPC) for a grid-connected wind farm paired to a hydrogen-based storage system (HESS) to produce hydrogen as a fuel for commercial road vehicles while meeting electric and contractual loads at the same time. In particular the integrated system (wind farm + HESS) should comply with the “fuel production” use case as per the IEA-HIA report where the hydrogen production for fuel cell electric vehicles (FCEVs) has the highest unconditional priority among all the objectives. Based on models adopting mixed-integer constraints and dynamics the problem of external hydrogen consumer requests optimal load demand tracking and electricity market participation is solved at different timescales to achieve a long-term plan based on forecasts that then are adjusted at real-time. The developed controller will be deployed onto the management platform of the HESS which is paired to a wind farm established in North Norway within the EU funded project HAEOLUS. Numerical analysis shows that the proposed controller efficiently manages the integrated system and commits the equipment so as to comply with the requirements of the addressed scenario. The operating costs of the devices are reduced by 5% which corresponds to roughly 300 commutations saved per year for devices.

Locomotives still use antiqued engines such as internal combustion engines operated by fossil fuels which cause global warming due to their significant emissions. This paper continues investigating the newly hybridized locomotive engine containing a gas turbine system solid oxide fuel cell system energy saving system and on-board hydrogen production system. This new engine is operated using five fuel blends composed of five alternative fuels such as hydrogen methane methanol ethanol and dimethyl ether. The current investigation involves exergy analysis exergo-economic analysis and exergo-environmental analysis to assess the engine from three perspectives: efficiency/irreversibility cost and environmental impact. The study results show that the net power of this new engine is 4948.6 kW and it has an exergetic efficiency of 62.7% according to the fuel and product principle. This engine weighs about 9 tons and costs about $10.2M with a levelized cost rate of 147 $/h and 14.06 mPt/h of overall component-related environmental rate. The average overall specific fuel and product exergy costs are about 37 $/GJ and 60 $/GJ and the minimum values are 13.3 $/GJ and 21.8 $/GJ using methane and hydrogen blend respectively. Also the average overall specific fuel and product exergo-environmental impact are about 15 and 23 mPt/MJ respectively. The on-board hydrogen production has an average exergy cost of 274 $/GJ and an environmental impact of 52 mPt/MJ. Hydrogen blended with methane or methanol is found to be more economic and has less environmental impact.

As result of the adverse effects caused by climate change the nations have decided to accelerate the transition of the energy matrix through the use of non-conventional sources free of polluting emissions. One of these alternatives is green hydrogen. In this context Chile stands out for the exceptional climate that makes it a country with a lot of renewable resources. Such availability of resources gives the nation clear advantages for hydrogen production strong gusts of wind throughout the country the most increased solar radiation in the world lower cost of production of electrical supplies among others. Due to this the nation would be between the lowest estimated cost for hydrogen production i.e. 1.5 USD/kg H2 approximately scenario that would place it as one of the cheapest green hydrogen producer in the world.

The shipping industry is a major enabler of globalization trade commerce and human welfare. But it is still heavily served by fossil fuels which make it one of the foremost greenhouse gas emitting sectors operational today. It is also one of the hardest to abate segments of the transport industry. As part of the economy-wide climate change mitigation and adaptation efforts it is necessary to consider a low carbon energy transition for this segment as well. This study examines the potential role of nuclear power and cogeneration towards greening this sector and identifies the associated techno-commercial and policy challenges associated with the transition. Quantitative estimates of the economics and investments associated with some of the possible routes are also presented. Alternatives such as nuclear-powered ships along commercial maritime trading routes ships working on nuclear derived green hydrogen ammonia or other sustainable power fuels will enable not only decarbonization of the shipping industry but also allow further diversification of the nuclear industry through non-electric applications of nuclear power and new sector coupling opportunities. In the run-up to the UNFCCC-COP28 meeting in 2023 in UAE nuclear equipped nations heavily engaged in and dependent on maritime trade and commerce should definitely consider nuclear driven decarbonization of shipping and some of the options presented here as part of their climate action strategies.

In this paper a novel process is developed to cogenerate 4741 kg/h of methanol 297.7 kW of electricity and 35.73 ton/h of hot water including a hydrogen purification system an absorption– compression refrigeration cycle (ACRC) a regenerative Organic Rankine Cycle (ORC) and parabolic solar troughs. The heat produced in the methanol reactor is recovered in the ORC and ACRC. Parabolic solar troughs provide thermal power to the methanol distillation tower. Thermal efficiencies of the integrated structure and the liquid methanol production cycle are 78.14% and 60.91% respectively. The process’s total exergy efficiency and irreversibility are 89.45% and 16.89 MW. The solar thermal collectors take the largest share of exergy destruction (34%) followed by heat exchangers (30%) and mixers (19%). Based on the sensitivity analysis D17 (mixture of H2 and low-pressure fuel gas before separation) was the most influential stream affecting the performance of the process. With the temperature decline of stream D17 from −139 to −149 °C the methanol production rate and the total thermal efficiency rose to 4741.2 kg/h and 61.02% respectively. Moreover the growth in the hydrogen content from 55% to 80% molar of the feed gas the flow rate of liquid methanol and the total exergy efficiency declined to 4487 kg/h and 86.05%.

Overview of advances in the technology of solid state hydrogen storage methods applying different kinds of novel materials is provided. Metallic and intermetallic hydrides complex chemical hydride nanostructured carbon materials metal-doped carbon nanotubes metal-organic frameworks (MOFs) metal-doped metal organic frameworks covalent organic frameworks (COFs) and clathrates solid state hydrogen storage techniques are discussed. The studies on their hydrogen storage properties are in progress towards positive direction. Nevertheless it is believed that these novel materials will offer far-reaching solutions to the onboard hydrogen storage problems in near future. The review begins with the deficiencies of current energy economy and discusses the various aspects of implementation of hydrogen energy based economy.

A viable hydrogen economy has thus far been hampered by the lack of an inexpensive and convenient hydrogen storage solution meeting all requirements especially in the areas of long hauls and delivery infrastructure. Current approaches require high pressure and/or complex heat management systems to achieve acceptable storage densities. Herein we present a manganese hydride molecular sieve that can be readily synthesized from inexpensive precursors and demonstrates a reversible excess adsorption performance of 10.5 wt% and 197 kgH₂ m^-3 at 120 bar at ambient temperature with no loss of activity after 54 cycles. Inelastic neutron scattering and computational studies confirm Kubas binding as the principal mechanism. The thermodynamically neutral adsorption process allows for a simple system without the need for heat management using moderate pressure as a toggle. A storage material with these properties will allow the DOE system targets for storage and delivery to be achieved providing a practical alternative to incumbents such as 700 bar systems which generally provide volumetric storage values of 40 kgH₂ m^-3 or less while retaining advantages over batteries such as fill time and energy density. Reasonable estimates for production costs and loss of performance due to system implementation project total energy storage costs roughly 5 times cheaper than those for 700 bar tanks potentially opening doors for increased adoption of hydrogen as an energy vector.

High-strength steel fasteners characterized by tensile strengths above 1100 MPa are often used in critical applications where a failure can have catastrophic consequences. Preventing hydrogen embrittlement (HE) failure is a fundamental concern implicating the entire fastener supply chain. Research is typically conducted under idealized conditions that cannot be translated into know-how prescribed in fastener industry standards and practices. Additionally inconsistencies and even contradictions in fastener industry standards have led to much confusion and many preventable or misdiagnosed fastener failures. HE susceptibility is a function of the material condition which is comprehensively described by the metallurgical and mechanical properties. Material strength has a first-order effect on HE susceptibility which increases significantly above 1200 MPa and is characterized by a ductile--brittle transition. For a given concentration of hydrogen and at equal strength the critical strength above which the ductile–brittle transition begins can vary due to second-order effects of chemistry tempering temperature and sub-microstructure. Additionally non-homogeneity of the metallurgical structure resulting from poorly controlled heat treatment impurities and non-metallic inclusions can increase HE susceptibility of steel in ways that are measurable but unpredictable. Below 1200 MPa non-conforming quality is often the root cause of real-life failures.

Link to document download on Royal Society Website 

Interest in blue hydrogen production technologies is growing. Some researchers have evaluated the environmental and/or economic feasibility of producing blue hydrogen but a holistic assessment is still needed. Many aspects of hydrogen production have not been investigated. There is very limited information in the literature on the impact of plant size on production and the extent of carbon capture on the cost and life cycle greenhouse gas (GHG) emissions of blue hydrogen production through various production pathways. Detailed uncertainty and sensitivity analyses have not been included in most of the earlier studies. This study conducts a holistic comparative cost and life cycle GHG emissions’ footprint assessment of three natural gas-based blue hydrogen production technologies – steam methane reforming (SMR) autothermal reforming (ATR) and natural gas decomposition (NGD) to address these research gaps. A hydrogen production plant capacity of 607 tonnes per day was considered. For SMR based on the percentage of carbon capture and capture points we considered two scenarios SMR-52% (indicates 52% carbon capture) and SMR-85% (indicates 85% carbon capture). A scale factor was developed for each technology to understand the hydrogen production cost with a change in production plant size. Hydrogen cost is 1.22 1.23 2.12 1.69 2.36 1.66 and 2.55 $/kg H2 for SMR ATR NGD SMR-52% SMR-85% ATR with carbon capture and sequestration (ATR-CCS) and NGD with carbon capture and sequestration (NGD-CCS) respectively. The results indicate that when uncertainty is considered SMR-52% and ATR are economically preferable to NGD and SMR-85%. SMR-52% could outperform ATR-CCS when the natural gas price decreases and the rate of return increases. SMR-85% is the least attractive pathway; however it could outperform NGD economically when CO2 transportation cost and natural gas price decrease. Hydrogen storage cost significantly impacts the hydrogen production cost. SMR-52% SMR-85% ATR-CCS and NGD-CCS have scale factors of 0.67 0.68 0.54 and 0.65 respectively. The hydrogen cost variation with capacity shows that operating SMR-52% and ATR-CCS above hydrogen capacity of 200 tonnes/day is economically attractive. Blue hydrogen from autothermal reforming has the lowest life cycle GHG emissions of 3.91 kgCO2eq/kg H2 followed by blue hydrogen from NGD (4.54 kgCO2eq/kg H2) SMR-85% (6.66 kgCO2eq/kg H2) and SMR-52% (8.20 kgCO2eq/kg H2). The findings of this study are useful for decision-making at various levels.

Greenhouse gas emissions from the freight transportation sector are a significant contributor to climate change pollution and negative health impacts because of the common use of heavy-duty diesel vehicles (HDVs). Governments around the world are working to transition away from diesel HDVs and to electric HDVs to reduce emissions. Battery electric HDVs and hydrogen fuel cell HDVs are two available alternatives to diesel engines. Each diesel engine HDV battery-electric HDV and hydrogen fuel cell HDV powertrain has its own advantages and disadvantages. This work provides a comprehensive review to examine the working mechanism performance metrics and recent developments of the aforementioned HDV powertrain technologies. A detailed comparison between the three powertrain technologies highlighting the advantages and disadvantages of each is also presented along with future perspectives of the HDV sector. Overall diesel engine in HDVs will remain an important technology in the short-term future due to the existing infrastructure and lower costs despite their high emissions while battery-electric HDV technology and hydrogen fuel cell HDV technology will be slowly developed to eliminate their barriers including costs infrastructure and performance limitations to penetrate the HDV market.

Unintended releases can occur during the production storage transportation and filling of liquid hydrogen which may cause devastating consequences. In the present work liquid hydrogen leak is modeled in ANSYS Fluent with the numerical model validated using the liquid hydrogen spill test data. A three-layer artificial neural network (ANN) model is built in which the wind speed ground temperature leakage time and leakage rate are taken as the inputs the horizontal diffusion distance and vertical diffusion distance of combustible gas as the outputs of the ANN. The representative sample data derived from the detailed calculation results of the numerical model are selected via the orthogonal experiment method to train and verify the back propagation (BP) neural network. Comparing the calculation results of the formula fitting with the sample data the results show that the established ANN model can quickly and accurately predict the horizontal and vertical diffusion distance of flammable vapor cloud relatively. The influences of four parameters on the horizontal hazard distance as well as vertical hazard height are predicted and analyzed in the case of continuous overflow of liquid hydrogen using the ANN model.

The computational thermodynamic analysis of a samarium oxide-based two-step solar thermochemical water splitting cycle is reported. The analysis is performed using HSC chemistry software and databases. The first (solar-based) step drives the thermal reduction of Sm2O3 into Sm and O2. The second (non-solar) step corresponds to the production of H2 via a water splitting reaction and the oxidation of Sm to Sm2O3. The equilibrium thermodynamic compositions related to the thermal reduction and water splitting steps are determined. The effect of oxygen partial pressure in the inert flushing gas on the thermal reduction temperature (TH) is examined. An analysis based on the second law of thermodynamics is performed to determine the cycle efficiency (ηcycle) and solar-to-fuel energy conversion efficiency (ηsolar´to´fuel) attainable with and without heat recuperation. The results indicate that ηcycle and ηsolar´to´fuel both increase with decreasing TH due to the reduction in oxygen partial pressure in the inert flushing gas. Furthermore the recuperation of heat for the operation of the cycle significantly improves the solar reactor efficiency. For instance in the case where TH = 2280 K ηcycle = 24.4% and ηsolar´to´fuel = 29.5% (without heat recuperation) while ηcycle = 31.3% and ηsolar´to´fuel = 37.8% (with 40% heat recuperation).

Green ammonia has potential as a zero-emissions energy vector in applications such as energy storage transmission and distribution and zero-emissions transportation. Renewable energy such as offshore wind energy has been proposed to power its production. This paper designed and analyzed an on-land small-scale power-to-ammonia (P2A) production system with a target nominal output of 15 tonnes of ammonia per day which will use an 8 MW offshore turbine system off the coast of Nova Scotia Canada as the main power source. The P2A system consists of a reverse osmosis system a proton exchange membrane (PEM) electrolyser a hydrogen storage tank a nitrogen generator a set of compressors and heat exchangers an autothermal Haber-Bosch reactor and an ammonia storage tank. The system uses an electrical grid as a back-up for when the wind energy is insufficient as the process assumes a steady state. Two scenarios were analyzed with Scenario 1 producing a steady state of 15 tonnes of ammonia per day and Scenario 2 being one that switched production rates whenever wind speeds were low to 55% the nominal capacity. The results show that the grid connected P2A system has significant emissions for both scenarios which is larger than the traditional fossil-fuel based ammonia production when using the grid in provinces like Nova Scotia even if it is just a back-up during low wind power generation. The levelized cost of ammonia (LCOA) was calculated to be at least 2323 CAD tonne−1 for both scenarios which is not cost competitive in this small production scale. Scaling up the whole system reducing the reliance on the electricity grid increasing service life and decreasing windfarm costs could reduce the LCOA and make this P2A process more cost competitive.

Severe accidents in nuclear power plants are potentially dangerous to both humans and the environment. To prevent and/or mitigate the consequences of these accidents it is paramount to have adequate accident management measures in place. During a severe accident combustible gases — especially hydrogen and carbon monoxide — can be released in significant amounts leading to a potential explosion risk in the nuclear containment building. These gases need to be managed to avoid threatening the containment integrity which can result in the releases of radioactive material into the environment. The main objective of the AMHYCO project is to propose innovative enhancements in the way combustible gases are managed in case of a severe accident in currently operating reactors. For this purpose the AMHYCO project pursues three specific activities including experimental investigations of relevant phenomena related to hydrogen / carbon monoxide combustion and mitigation with PARs (Passive Autocatalytic Recombiners) improvement of the predictive capabilities of analysis tools used for explosion hazard evaluation inside the reactor containment as well as enhancement of the Severe Accident Management Guidelines (SAMGs) with respect to combustible gases risk management based on theoretical and experimental results. Officially launched on 1 October 2020 AMHYCO is an EU-funded Horizon 2020 project that will last 4 years from 2020 to 2024. This international project consists of 12 organizations (six from European countries and one from Canada) and is led by the Universidad Politécnica de Madrid (UPM). AMHYCO will benefit from the worldwide experts in combustion science accident management and nuclear safety in its Advisory Board. The paper will give an overview of the work program and planned outcome of the project.

In water-cooled nuclear power plants hydrogen gas can be generated by various mechanisms during an accident. In case combustion of the resulting hydrogen-air mixture within the facility occurs existing containment structures may be compromised and excessive radio-active material can be released to the environment. Thus an improved understanding of the propagation of lean hydrogen deflagrations within buildings and structures is essential for the development of appropriate accident management strategies associated with these scenarios. Following the accident in Fukushima Japan the application of three-dimensional computational fluid dynamics methods to high-fidelity detailed analysis of hydrogen combustion processes in both closed and vented vessels has become more widespread. In this study a recently developed large-eddy-simulation (LES) capability is applied to the prediction of lean premixed hydrogen deflagrations in vented vessels. The LES methodology makes use of a flamelet- or progress-variable-based combustion model coupled with an empirical burning velocity model (BVM) an anisotropic block-based adaptive mesh refinement (AMR) strategy an accurate finite-volume numerical scheme and a mesh independent subfilter-scale (SFS) model. Several different vessel and vent sizes and configurations are considered herein. The LES predictions are compared to experimental data obtained from the Large-Scale Vented Combustion Test Facility (LSVCTF) of the Canadian Nuclear Laboratories (CNL) with both quiescent and turbulent initial conditions. Following descriptions of the LES models LES results for both variable chamber sizes and single- and double-vent cases are presented to illustrate the capabilities of the proposed computational approach. In particular the predicted time histories of pressure as well as the maximum overpressure achieved within the vessels and combustion compartments are compared to those from the LSVCTF experiments. The influences of the modelled ignition process initial turbulence and mesh resolution on the LES results are also discussed. The findings highlight the potential and limitations of the proposed LES approach for accurately describing lean premixed hydrogen deflagrations within vented vessels.

Hydrogen recombiners (known in the nuclear industry as passive autocatalytic recombiners-PARs) in general can be utilized for mitigation of hydrogen in controlled areas where there is potential for hydrogen release and ventilation is not practical. Recombiners are widely implemented in the nuclear industry however there are other applications of recombiners outside the nuclear industry that have not yet been explored practically. The most notable benefit of recombiners over conventional hydrogen mitigation measures is their passive capability where power or operator actions are not needed for the equipment to remove hydrogen when it is present.

One of most significant concerns regarding the use of hydrogen recombiners in industry is their potential to ignite hydrogen at elevated concentrations (>6 vol%). The catalyst heated by the exothermal H2–O2 reaction is known to be a potential ignition source to cause hydrogen burns. An experimental program utilizing a full-size PAR at the Large-Scale Vented Combustion Test Facility (LSVCTF) has been carried out by Canadian Nuclear Laboratories (CNL) to investigate and understand the behaviour of hydrogen combustion induced by a PAR on a large-scale basis. A number of parameters external to the PAR have been explored including the effect of ambient humidity (steam) and temperature. The various aspects of this investigation will be discussed in this paper and examples of results are provided.