Production & Supply Chain

Preventing humanity from serious impact of climate crisis requires carbon neutrality across all economic sectors including steel industry. Although fossil-free steelmaking routes receiving increasing attention fundamental process aspects especially approaches towards the improvement of efficiency and flexibility are so far not comprehensively studied. In this paper optimized process concepts allowing for a gradual transition towards fossil-free steelmaking based on the coupling of direct reduction process electric arc furnace and electrolysis are presented. Both a high-temperature and low-temperature electrolysis were modeled and possibilities for the integration into existing infrastructure are discussed. Various schemes for heat integration especially when using high-temperature electrolysis are highlighted and quantified. It is demonstrated that the considered direct reduction-based process concepts allow for a high degree of flexibility in terms of feed gas composition when partially using natural gas as a bridge technology. This allows for an implementation in the near future as well as the possibility of supplying power grid services in a renewable energy system. Furthermore it is shown that an emission reduction potential of up to 97.8% can be achieved with a hydrogen-based process route and 99% with a syngas-based process route respectively provided that renewable electricity is used.

The most profitable offshore energy resources are usually found away from the coast. Nevertheless the accessibility and grid integration in those areas are more complicated. To avoid this problematic large scale hydrogen production is being promoted for far offshore applications. The main objective of this paper is to analyze the ability of wave energy converters to maximize hydrogen production in hybrid wind and wave far offshore farms. To that end wind and wave resource data are obtained from ERA5 for different locations in the Atlantic ocean and a Maximum Covariance Analysis is proposed for the selection of the most representative locations. Furthermore the suitability of different sized wave energy converters for auxiliary hydrogen production in the far offshore wind farms is also analysed. On that account the hydrodynamic parameters of the oscillating bodies are obtained via simulations with a Boundary Element Method based code and their operation is modelled using the software tool Matlab. The combination of both methodologies enables to perform a realistic assessment of the contribution of the wave energy converters to the hydrogen generation of an hybrid energy farm especially during those periods when the wind turbines would be stopped due to the variability of the wind. The obtained results show a considerable hydrogen generation capacity of the wave energy converters up to 6.28% of the wind based generation which could remarkably improve the efficiency of the far offshore farm and bring important economical profit. Wave energy converters are observed to be most profitable in those farms with low covariance between wind and waves where the disconnection times of the wind turbines are prone to be more prolonged but the wave energy is still usable. In such cases a maximum of 101.12 h of equivalent rated production of the wind turbine has been calculated to be recovered by the wave energy converters.

Water electrolysis is a promising technology for enabling the storage of surplus electricity produced by intermittent renewable power sources in the form of hydrogen. At the core of this technology is the electrolyte and whether this is acidic or alkaline affects the reaction mechanisms gas purities and is of significant importance for the stability and activity of the electrocatalysts. This article presents a simple but precise physical model to describe the voltage-current characteristic heat balance gas crossover and cell efficiency of water electrolyzers. State-of-the-art water electrolysis cells with acidic and alkaline electrolyte are experimentally characterized in order to parameterize the model. A rigorous comparison shows that alkaline water electrolyzers with Ni-based catalysts but thinner separators than those typically used is expected be more efficient than acidic water electrolysis with Ir and Pt based catalysts. This performance difference was attributed mainly to a similar conductivity but approximately 38-fold higher diffusivities of hydrogen and oxygen in the acidic polymer electrolyte membrane (Nafion) than those in the alkaline separator (Zirfon filled with a 30 wt% KOH solution). With reference to the detailed analysis of the cell characteristics perspectives for the improvement of the efficiency of water electrolyzers are discussed.

Currently a progressively different approach to the generation of power and the production of fuels for the automotive sector as well as for domestic applications is being taken. As a result research on the feasibility of applying renewable energy sources to the present energy scenario has been progressively growing aiming to reduce greenhouse gas emissions. Following more than one approach the integration of renewables mainly involves the utilization of biomass-derived raw material and the combination of power generated via clean sources with conventional power generation systems. The aim of this review article is to provide a satisfactory overview of the most recent progress in the catalysis of hydrogen production through sustainable reforming and CO2 utilization. In particular attention is focused on the route that starting from bioethanol reforming for H2 production leads to the use of the produced CO2 for different purposes and by means of different catalytic processes passing through the water–gas shift stage. The newest approaches reported in the literature are reviewed showing that it is possible to successfully produce “green” and sustainable hydrogen which can represent a power storage technology and its utilization is a strategy for the integration of renewables into the power generation scenario. Moreover this hydrogen may be used for CO2 catalytic conversion to hydrocarbons thus giving CO2 added value.

Given that conversion efficiencies of incident solar radiation to liquid fuels e.g. H2 are of the order of a few percent or less as quantified by ‘solar to hydrogen’ (STH) economically inexpensive and operationally straightforward ways to boost photo-electrochemcial (PEC) H2 production from solar-driven water splitting are important. In this work externally-applied static electric fields have led to enhanced H2 production in an energy-efficient manner with up to ~30–40% increase in H2 (bearing in mind fieldinput energy) in a prototype open-type solar cell featuring rutile/titania and hematite/iron-oxide (Fe2O3) respectively in contact with an alkaline aqueous medium (corresponding to respective relative increases of STH by ~12 and 16%). We have also performed non-equilibrium ab-initio molecular dynamics in both static electric and electromagnetic (e/m) fields for water in contact with a hematite/iron-oxide (0 0 1) surface observing enhanced break-up of water molecules by up to ~70% in the linear-response régime. We discuss the microscopic origin of such enhanced water-splitting based on experimental and simulation-based insights. In particular we external-field direction at the hematite surfaces and scrutinise properties of the adsorbed water molecules and OH– and H3O+ species e.g. hydrogen bonds between water-protons and the hematite surfaces’ bridging oxygen atoms as well as interactions between oxygen atoms in adsorbed water molecules and underlying iron atoms.

Supercritical water gasification is a promising technology for wet biomass utilization. In this paper Ni and other metal catalysts were synthesized by wet impregnation. The stability and catalytic activities of Ni catalysts were evaluated. Firstly catalytic activities of Ni Fe Cu catalysts supported on MgO were tested using wheat straw as raw material in a batch reactor at 723 K and water density of 0.07 cm³/g. Experimental results showed that the order of metal catalyst activity for hydrogen generation was Ni/MgO > Fe/MgO > Cu/MgO. Secondly the influence of different supports on Ni catalysts performance was investigated. The results showed that the order of the Ni catalysts’ activity with different supports was Ni/MgO > Ni/ZnO > Ni/Al2O3 > Ni/ZrO2. Finally the effects of Ni loading and the amount of Ni catalyst addition on hydrogen production and the stability of Ni/MgO catalyst were studied. It was found that serious deactivation of Ni catalyst in the process of supercritical water gasification took place. Even if carbon deposited on the catalyst surface was removed by high temperature calcination and the catalyst was reduced with hydrogen the activity of used catalyst was only partially restored.

Biogas is one of the most important sources of renewable energy and hydrogen production which needs upgrading to be functional. In this study two methods of biogas upgrading from organic parts of municipal waste were investigated. For biogas upgrading this article used a 3E analysis and simulated cryogenic separation and chemical scrubbing. The primary goal was to compare thermoeconomic indices and create hydrogen by reforming biomethane. The exergy analysis revealed that the compressor of the refrigerant and recovery column of MEA contributed the most exergy loss in the cryogenic separation and chemical scrubbing. The total exergy efficiency of cryogenic separation and chemical scrubbing was 85% and 84%. The energy analysis revealed a 2.07% lower energy efficiency for chemical scrubbing. The capital energy and total annual costs of chemical absorption were 56.51 26.33 and 54.44 percent lower than those of cryogenic separation respectively indicating that this technology is more economically feasible. Moreover because the thermodynamic efficiencies of the two methods were comparable the chemical absorption method was adopted for hydrogen production. The biomethane steam reforming was simulated and the results indicated that this method required an energy consumption of 90.48 MJ kgH2 . The hydrogen production intensity equaled 1.98 kmoleH2 kmolebiogas via a 79.92% methane conversion.

In this paper a new gasification system is developed for the three useful outputs of electricity heat and hydrogen and reported for practical energy applications. The study also investigates the composition of syngas leaving biomass gasifier. The composition of syngas is represented by the fractions of hydrogen carbon dioxide carbon monoxide and water. The integrated energy system comprises of an entrained flow gasifier a Cryogenic Air Separation (CAS) unit a double-stage Rankine cycle Water Gas Shift Reactor (WGSR) a combined gas–steam power cycle and a Proton Exchange Membrane (PEM) electrolyzer. The whole integrated system is modeled in the Aspen plus 9.0 excluding the PEM electrolyzer which is modeled in Engineering Equation Solver (EES). A comprehensive parametric investigation is conducted by varying numerous parameters like biomass flow rate steam flow rate air input flow rate combustion reactor temperature and power supplied to the electrolyzer. The system is designed in a way to supply the power produced by the steam Rankine cycle to the PEM electrolyzer for hydrogen production. The overall energy efficiency is obtained to be 53.7% where the exergy efficiency is found to be 45.5%. Furthermore the effect of the biomass flow rate is investigated on the various system operational parameters.

Dry reforming of hydrocarbons alcohols and biological compounds is one of the most promising and effective avenues to increase hydrogen (H2 ) production. Catalytic dry reforming is used to facilitate the reforming process. The most popular catalysts for dry reforming are Ni-based catalysts. Due to their inactivation at high temperatures these catalysts need to use metal supports which have received special attention from researchers in recent years. Due to the existence of a wide range of metal supports and the need for accurate detection of higher H2 production in this study a systematic review and meta-analysis using ANNs were conducted to assess the hydrogen production by various catalysts in the dry reforming process. The Scopus Embase and Web of Science databases were investigated to retrieve the related articles from 1 January 2000 until 20 January 2021. Forty-seven articles containing 100 studies were included. To determine optimal models for three target factors (hydrocarbon conversion hydrogen yield and stability test time) artificial neural networks (ANNs) combined with differential evolution (DE) were applied. The best models obtained had an average relative error for the testing data of 0.52% for conversion 3.36% for stability and 0.03% for yield. These small differences between experimental results and predictions indicate a good generalization capability.

This paper describes a generic and systematic method to calculate the efficiency and the annual performance for Power-to-Gas (PtG) systems. This approach gives the basis to analytically compare different PtG systems using different technologies under different boundary conditions. To have a comparable basis for efficiency calculations a structured break down of the PtG system is done. Until now there has not been a universal approach for efficiency calculations. This has resulted in a wide variety of efficiency calculations used in feasibility studies and for business-case calculations. For this the PtG system is divided in two sub-systems: the electrolysis and the methanation. Each of the two sub-systems consists of several subsystem boundary levels. Staring from the main unit i.e. the electrolysis stack and/or methanation reactor further units that are required to operate complete PtG system are considered with their respective subsystem boundary conditions. The paper provides formulas how the efficiency of each level can be calculated and how efficiency deviations can be integrated which are caused by the extended energy flow calculations to and from energy users and thermal losses. By this a sensitivity analysis of the sub-systems can be gained and comprehensive goal functions for optimizations can be defined. In a second step the annual performance of the system is calculated as the ratio of useable output and energetic input over one year. The input is the integral of the annual need of electrical and thermal energy of a PtG system depending on the different operation states of the plant. The output is the higher heating value of the produced gas and – if applicable – heat flows that are used externally. The annual performance not only evaluates the steady-state operating efficiency under full load but also other states of the system such as cold standby or service intervals. It is shown that for a full system operation assessment and further system concept development the annual performance is of much higher importance than the steady-state system efficiency which is usually referred to. In a final step load profiles are defined and the annual performance is calculated for a specific system configuration. Using this example different operation strategies are compared.