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Biofuel in Ghana: Potentials and strategies for policy implementation
Pub Date : 2025-01-25 DOI: 10.1016/j.jfueco.2025.100134
Stephen Kelly Kissi , Wilson Ofori Sarkodie , Mohammed Takase , Emmanuel Amankwah
Africa has a pressing need for biofuel policies due to several interconnected challenges encompassing vulnerability to price fluctuations, rural development, waste and land use management, and the need for value-added agricultural goods. State biofuel policies contribute to the ongoing global discourse on climate change, green and circular economy, and sustainability. Unfortunately, the resource curse seems to have befallen the Ghanaian economy as the nation still imports petroleum products after discovering enormous oil reserves. This article reviews Ghana's current biomass potential drawing lessons from failed projects and initiatives of top biofuel nations to effectively implement Ghana's latest biofuel policy. A significant portion of land in Ghana remains unused, yet utilizing less than 3 % of this land would be sufficient to meet the B10/E10 biofuel target using cassava as the feedstock. A closer examination of successful biofuel initiatives in Brazil and the United States highlights common factors contributing to their achievements. These include ambitious blending mandates, substantial investments in infrastructure, technology, and research, active stakeholder participation, and the provision of fiscal incentives. While Ghana's Renewable Energy Master Plan incorporates some of these components, its current targets lack sufficient ambition. Addressing these gaps in practice could place Ghana on a trajectory toward becoming one of the world's leading biofuel producers.
{"title":"Biofuel in Ghana: Potentials and strategies for policy implementation","authors":"Stephen Kelly Kissi ,&nbsp;Wilson Ofori Sarkodie ,&nbsp;Mohammed Takase ,&nbsp;Emmanuel Amankwah","doi":"10.1016/j.jfueco.2025.100134","DOIUrl":"10.1016/j.jfueco.2025.100134","url":null,"abstract":"<div><div>Africa has a pressing need for biofuel policies due to several interconnected challenges encompassing vulnerability to price fluctuations, rural development, waste and land use management, and the need for value-added agricultural goods. State biofuel policies contribute to the ongoing global discourse on climate change, green and circular economy, and sustainability. Unfortunately, the resource curse seems to have befallen the Ghanaian economy as the nation still imports petroleum products after discovering enormous oil reserves. This article reviews Ghana's current biomass potential drawing lessons from failed projects and initiatives of top biofuel nations to effectively implement Ghana's latest biofuel policy. A significant portion of land in Ghana remains unused, yet utilizing less than 3 % of this land would be sufficient to meet the B10/E10 biofuel target using cassava as the feedstock. A closer examination of successful biofuel initiatives in Brazil and the United States highlights common factors contributing to their achievements. These include ambitious blending mandates, substantial investments in infrastructure, technology, and research, active stakeholder participation, and the provision of fiscal incentives. While Ghana's Renewable Energy Master Plan incorporates some of these components, its current targets lack sufficient ambition. Addressing these gaps in practice could place Ghana on a trajectory toward becoming one of the world's leading biofuel producers.</div></div>","PeriodicalId":100556,"journal":{"name":"Fuel Communications","volume":"22 ","pages":"Article 100134"},"PeriodicalIF":0.0,"publicationDate":"2025-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143134530","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chemical agents for enhanced oil recovery: A comparison of a switchable hydrophilic solvent and deep eutectic solvent
Pub Date : 2025-01-12 DOI: 10.1016/j.jfueco.2025.100133
A. Abdurrahman , S.M. Shuwa , F.N. Dabai , O.D. Orodu , F.T. Ogunkunle , A.I. Igbafe , B.Y. Jibril
Switchable hydrophilic solvents (SHS) and deep eutectic solvents (DES) are trending chemical agents used in enhanced oil recovery. In this study, the oil recovery performance of DES, synthesized from tetrabutylammonium bromide (TBAB) and polyethylene glycol 400 (PEG 400) in a 1:2 molar ratio, and the switchable solvent N,N-dimethylcyclohexylamine (DMCHA) was evaluated through a displacement test. Additionally, the interactions between the rock, solvents, and crude oil were investigated through interfacial tension (IFT) measurements using an Altension tensiometer. The trend in the experimental IFT results was compared to the interactions between DMCHA and oil, DMCHA and rock, DES and oil, and DES and rock using quantum mechanics calculations performed with the Spartan v20 molecular modeling tool. The findings revealed that the IFT between the solvents and oil decreased to 5.32 mN/m with DES and 2.64 mN/m with DMCHA. Furthermore, core flooding experiments showed an incremental recovery of 12.0 % of the original oil in place (OOIP) with DES and 10.0 % OOIP with DMCHA for standard Berea sandstone core samples. Similarly, flooding experiments using Niger-Delta sandstone samples achieved an additional 25.8 % OOIP with DES compared to 12.0 % OOIP with DMCHA. In conclusion, both DES and DMCHA demonstrated their potential for crude oil recovery. However, DES proved to be more promising for tertiary enhanced oil recovery applications.
{"title":"Chemical agents for enhanced oil recovery: A comparison of a switchable hydrophilic solvent and deep eutectic solvent","authors":"A. Abdurrahman ,&nbsp;S.M. Shuwa ,&nbsp;F.N. Dabai ,&nbsp;O.D. Orodu ,&nbsp;F.T. Ogunkunle ,&nbsp;A.I. Igbafe ,&nbsp;B.Y. Jibril","doi":"10.1016/j.jfueco.2025.100133","DOIUrl":"10.1016/j.jfueco.2025.100133","url":null,"abstract":"<div><div>Switchable hydrophilic solvents (SHS) and deep eutectic solvents (DES) are trending chemical agents used in enhanced oil recovery. In this study, the oil recovery performance of DES, synthesized from tetrabutylammonium bromide (TBAB) and polyethylene glycol 400 (PEG 400) in a 1:2 molar ratio, and the switchable solvent N,N-dimethylcyclohexylamine (DMCHA) was evaluated through a displacement test. Additionally, the interactions between the rock, solvents, and crude oil were investigated through interfacial tension (IFT) measurements using an Altension tensiometer. The trend in the experimental IFT results was compared to the interactions between DMCHA and oil, DMCHA and rock, DES and oil, and DES and rock using quantum mechanics calculations performed with the Spartan v20 molecular modeling tool. The findings revealed that the IFT between the solvents and oil decreased to 5.32 mN/m with DES and 2.64 mN/m with DMCHA. Furthermore, core flooding experiments showed an incremental recovery of 12.0 % of the original oil in place (OOIP) with DES and 10.0 % OOIP with DMCHA for standard Berea sandstone core samples. Similarly, flooding experiments using Niger-Delta sandstone samples achieved an additional 25.8 % OOIP with DES compared to 12.0 % OOIP with DMCHA. In conclusion, both DES and DMCHA demonstrated their potential for crude oil recovery. However, DES proved to be more promising for tertiary enhanced oil recovery applications.</div></div>","PeriodicalId":100556,"journal":{"name":"Fuel Communications","volume":"22 ","pages":"Article 100133"},"PeriodicalIF":0.0,"publicationDate":"2025-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143134532","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Properties and Autoignition reactivity of diesel boiling range ethers produced from Guerbet alcohols
Pub Date : 2024-12-22 DOI: 10.1016/j.jfueco.2024.100131
Robert L. McCormick , Jon Luecke , Samah Y. Mohamed , Gina M. Fioroni , Nimal Naser , Teresa L. Alleman , Seonah Kim , Michael P. Lanci , Kenneth Kar
We examine the properties of diesel boiling range ethers made from coupling of alcohols produced by oligomerization of ethanol (Guerbet alcohols) for their utility as low-carbon liquid fuel blendstocks. Basic properties of boiling point, flash point, freezing point, density and viscosity are well suited for blending into diesel fuels. For the mixture of ethers the lightest component, di-n-butyl ether, can be present at up to 20 vol% while still having adequately high flashpoint for safe handling. Soot formation tendency (as yield sooting index) is well below that of conventional diesel. The ethers have similar compatibility with elastomers as conventional diesel, based on Hansen solubility parameter analysis. Oxidation stability was assessed for 30 vol% blends of individual ethers in a conventional diesel fuel using a long-term storage test. Over 6 weeks we observed no formation of peroxides or degradation. n-alkyl ethers with carbon number of 8 or higher have cetane number over 100, which is outside the defined range of cetane number, while branched ethers are over 70. The ethers also blend antagonistically into conventional diesel for cetane number, meaning that the blend cetane value is lower than predicted based on a linear by volume, mass, or mole model. We show that aromatics and naphthenes likely act as radical scavengers to slow or shut down autoignition of the highly reactive ethers at low to medium blend levels. Overall, diesel boiling range ethers show significant promise as high quality low-net carbon diesel blendstocks.
{"title":"Properties and Autoignition reactivity of diesel boiling range ethers produced from Guerbet alcohols","authors":"Robert L. McCormick ,&nbsp;Jon Luecke ,&nbsp;Samah Y. Mohamed ,&nbsp;Gina M. Fioroni ,&nbsp;Nimal Naser ,&nbsp;Teresa L. Alleman ,&nbsp;Seonah Kim ,&nbsp;Michael P. Lanci ,&nbsp;Kenneth Kar","doi":"10.1016/j.jfueco.2024.100131","DOIUrl":"10.1016/j.jfueco.2024.100131","url":null,"abstract":"<div><div>We examine the properties of diesel boiling range ethers made from coupling of alcohols produced by oligomerization of ethanol (Guerbet alcohols) for their utility as low-carbon liquid fuel blendstocks. Basic properties of boiling point, flash point, freezing point, density and viscosity are well suited for blending into diesel fuels. For the mixture of ethers the lightest component, di-n-butyl ether, can be present at up to 20 vol% while still having adequately high flashpoint for safe handling. Soot formation tendency (as yield sooting index) is well below that of conventional diesel. The ethers have similar compatibility with elastomers as conventional diesel, based on Hansen solubility parameter analysis. Oxidation stability was assessed for 30 vol% blends of individual ethers in a conventional diesel fuel using a long-term storage test. Over 6 weeks we observed no formation of peroxides or degradation. n-alkyl ethers with carbon number of 8 or higher have cetane number over 100, which is outside the defined range of cetane number, while branched ethers are over 70. The ethers also blend antagonistically into conventional diesel for cetane number, meaning that the blend cetane value is lower than predicted based on a linear by volume, mass, or mole model. We show that aromatics and naphthenes likely act as radical scavengers to slow or shut down autoignition of the highly reactive ethers at low to medium blend levels. Overall, diesel boiling range ethers show significant promise as high quality low-net carbon diesel blendstocks.</div></div>","PeriodicalId":100556,"journal":{"name":"Fuel Communications","volume":"22 ","pages":"Article 100131"},"PeriodicalIF":0.0,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143134531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Assessment of potential sites for biogas production plants from domestic, agricultural, and livestock waste
Pub Date : 2024-12-22 DOI: 10.1016/j.jfueco.2024.100132
Rahim Moltames , Younes Noorollahi , Hossein Yousefi , Behzad Azizimehr , Amir Naseri
Employing biomass energy can potentially play a key role in decreasing the environmental effects of non-renewable energy sources, especially global warming and its consequences. However, the availability of agricultural biomass, municipal garbage, and livestock waste is locally dispersed. The spatial distribution of these resources and the associated collection and transportation costs are the most important critical points for the success of the biomass power conversion facility. The biomass, scattered and loose, has a large cost of collecting and transporting, which can be reduced by proper planning and locating biomass collection centers and biomass-based power plants. Before planning collection centers, it is essential to assess biomass, energy, and the cost of biomass collection in this field. In this study, the biomass feed potential is evaluated using a Geographic Information System (GIS) to identify sites with biomass feed input capacity. Using the transport planning method, the best city to build the biomass power plant is specified.
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引用次数: 0
Effects of difference in heating sources on ammonia reactivity: Possibility for photolysis-assisted ammonia combustion 不同加热源对氨反应性的影响:光解辅助氨燃烧的可能性
Pub Date : 2024-09-06 DOI: 10.1016/j.jfueco.2024.100130
Kenta Tamaoki , Yoshito Ishida , Takuya Tezuka , Hisashi Nakamura

Ammonia (NH3) reactivity in a micro flow reactor with a controlled temperature profile (MFR) is reexamined through species measurements utilizing two heating sources in the MFR: an H2/air flat flame and an electric heater. The maximum wall temperatures (Tw,max) formed in the reactor vary in a range of Tw,max = 1100–1400 K. A stoichiometric NH3/air mixture is tested, and exhaust NH3 is detected by a quadrupole mass spectrometer (QMS). Unexpectedly, NH3 is completely consumed at temperatures at least 100 K lower in the H2/air flat flame case compared to the electric furnace case, despite nearly identical conditions of a MFR characteristic residence time estimated by the wall temperature profiles and the convective flow velocity. Considering the non-thermal characteristics of the two heating sources that the H2/air flat flame emits ultraviolet light, whereas infrared light as thermal radiation is emitted within the electric furnace, the possibility of NH3 photolysis in the H2/air flat flame case is discussed based on literature regarding emissions from the H2/air flames, the transmittance of the quartz tube, and the photodissociation of NH3 in the ultraviolet region. When ultraviolet light emitted from the H2/air flat flame passes through the quartz tube and decomposes NH3 into NH2 and H radicals, these produced radicals enhance the growth of OH radicals, resulting in increased NH3 reactivity. These findings suggest the possibility of photolysis-assisted ammonia combustion, which could be an additional method to overcome the low reactivity of NH3.

通过利用 MFR 中的两种加热源(H2/空气平焰和电加热器)进行物种测量,重新研究了温度曲线受控的微流反应器(MFR)中的氨(NH3)反应性。反应器中形成的最高壁温(Tw,max)在 Tw,max = 1100-1400 K 的范围内变化。出乎意料的是,尽管根据壁温曲线和对流流速估算的 MFR 特性停留时间条件几乎相同,但与电炉相比,H2/空气平焰情况下 NH3 的完全消耗温度至少低 100 K。考虑到两种加热源的非热特性,即 H2/air 平焰发射紫外线,而电炉内则发射作为热辐射的红外线,根据有关 H2/air 火焰发射、石英管透射率和 NH3 在紫外线区域光解的文献,讨论了在 H2/air 平焰情况下 NH3 光解的可能性。当 H2/air 平面火焰发出的紫外线穿过石英管并将 NH3 分解为 NH2 和 H 自由基时,这些产生的自由基会促进 OH 自由基的生长,从而提高 NH3 的反应活性。这些发现表明了光解辅助氨燃烧的可能性,这可能是克服 NH3 反应性低的另一种方法。
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引用次数: 0
Investigations on conical lean turbulent premixed hydrogenated natural gas flames 锥形贫化湍流预混合加氢天然气火焰研究
Pub Date : 2024-07-11 DOI: 10.1016/j.jfueco.2024.100128
Dilay Güleryüz , Christophe Allouis , İskender Gökalp

Hydrogen's ability to enhance carbon neutrality in combustion processes puts forward the use of hydrogenated fuels, both in the form of fuel and an energy carrier as a potential decarbonization solution. However, because of the nature of hydrogen, blending it with hydrocarbons causes crucial structural changes in the flame structure, including higher flame propagation velocities and higher flame temperatures, decreased instantaneous flame thickness, and increased risks of flame flashback and an increasing potential of NOx emissions due to higher flame temperatures. These attributes encourage a thorough examination of hydrogenated blends of hydrocarbon fuels. Using lean premixed fuels is another technique to achieve efficient and cleaner combustion. However, due to the problem of flame instability in lean premixed combustion, forecasting the design points in terms of flame attributes is critical for better combustor designs.

In this study, conical (Bunsen type) lean premixed turbulent flames of hydrogenated natural gas-air mixtures are experimentally studied. Through chemiluminescence measurements of the OH* and CH* radicals and laser-induced Mie scattering, lean natural gas-air premixed flames are examined with subsequently increasing hydrogen addition rates up to 20% by volume and keeping the premixture velocity constant. The obtained data is utilized for exploring the dynamics of the turbulent flame front. The main turbulent premixed flame parameters we identified relate to the instantaneous and average topology of the flame such as the turbulent flame brush thickness and flame height. We also inferred global combustion parameters like the turbulent flame propagation speed from the experimental findings.

氢气能够提高燃烧过程中的碳中性,因此氢化燃料的使用,无论是作为燃料还是作为能源载体,都是一种潜在的脱碳解决方案。然而,由于氢的特性,氢与碳氢化合物混合会导致火焰结构发生重大变化,包括火焰传播速度加快、火焰温度升高、瞬时火焰厚度减小、火焰回火风险增加以及火焰温度升高导致氮氧化物排放潜力增加。这些特性促使我们对碳氢化合物燃料的加氢混合物进行彻底研究。使用贫油预混燃料是实现高效清洁燃烧的另一种技术。然而,由于贫油预混燃烧中的火焰不稳定性问题,预测火焰属性方面的设计点对于更好地设计燃烧器至关重要。本研究对加氢天然气-空气混合物的锥形(本生型)贫油预混湍流火焰进行了实验研究。通过对 OH* 和 CH* 自由基的化学发光测量以及激光诱导 Mie 散射,研究了在保持预混速度不变的情况下,随着氢气添加率的增加(按体积计算最高可达 20%),贫天然气-空气预混合火焰的情况。获得的数据用于探索湍流火焰前沿的动态。我们确定的主要湍流预混火焰参数与火焰的瞬时和平均拓扑结构有关,如湍流火焰刷厚度和火焰高度。我们还从实验结果中推断出了湍流火焰传播速度等全局燃烧参数。
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引用次数: 0
Diversity in the acceptance of sustainable aviation fuels: Uncovering varying motivational patterns 接受可持续航空燃料的多样性:发现不同的动机模式
Pub Date : 2024-07-10 DOI: 10.1016/j.jfueco.2024.100129
Eva-Maria Schomakers, Linda Engelmann, Martina Ziefle

The aviation sector’s significant contribution to greenhouse gas emissions has spurred interest in sustainable aviation fuels (SAF) as a means to mitigate environmental impact. This study examines user diversity in the public acceptance of power-to-liquid aviation fuels (eSAF), exploring varying attitudes towards the environment, flying, and eSAF adoption. Through a quantitative survey of a representative German sample, three distinct segments emerged: the Environment-Centered Approvers, the Flying-Centered Approvers, and the Skeptical. The Environment-Centered Approvers prioritize environmental concerns and perceive moral obligations to use eSAF for climate protection. In contrast, the Flying-Centered Approvers prioritize the continuation of flying with reduced environmental impact, while the Skeptical exhibit a more cautious and uncertain stance towards eSAF adoption. The study highlights the importance of tailoring communication strategies based on the unique motivations and concerns of each subgroup to effectively promote eSAF adoption.

航空业对温室气体排放贡献巨大,这激发了人们对可持续航空燃料(SAF)作为减轻环境影响手段的兴趣。本研究考察了公众对动力液化航空燃料(eSAF)接受程度的用户多样性,探讨了对环境、飞行和采用 eSAF 的不同态度。通过对具有代表性的德国样本进行定量调查,发现了三个不同的群体:以环境为中心的赞同者、以飞行为中心的赞同者和持怀疑态度的人。以环境为中心的赞同者将环境问题放在首位,并认为有道德义务使用 eSAF 来保护气候。相比之下,以飞行为中心的赞同者优先考虑的是在减少环境影响的情况下继续飞行,而持怀疑态度的人则对采用 eSAF 表现出更加谨慎和不确定的态度。这项研究强调了根据每个子群体的独特动机和关注点来定制传播策略的重要性,以有效促进 eSAF 的采用。
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引用次数: 0
Flame stabilization and pollutant emissions of turbulent ammonia and blended ammonia flames: A review of the recent experimental and numerical advances 湍流氨和混合氨火焰的火焰稳定和污染物排放:近期实验和数值研究进展综述
Pub Date : 2024-07-07 DOI: 10.1016/j.jfueco.2024.100127
Mahmoud M.A. Ahmed , Leilei Xu , Xue-Song Bai , Zubayr O. Hassan , Marwan Abdullah , Jaeheon Sim , Emre Cenker , W.L. Roberts , A.M. Elbaz

Compared to traditional hydrocarbon fuels, ammonia presents significant challenges as a fuel, including high ignition energy, low reactivity, slow flame propagation, and high NOx emissions, which hinder its use as a renewable fuel. Blending ammonia with fossil fuels like natural gas improves its combustion reactivity and helps mitigate CO2 emissions. However, there is still much to understand about the complex dynamics of ammonia and its blends with hydrocarbons. Key areas such as reaction kinetics mechanisms, ignition properties, flame propagation behaviors, and methods for controlling combustion performance under various conditions require further elucidation. This paper reviews recent advancements in experiments and numerical simulations aimed at developing stable, and low-emission combustors for ammonia-fired power generation. Recent burner and flame configurations, including non-swirling jets, single-stage swirl burners, two-stage burners, and newly developed double-swirl burners are analyzed for their flame stability and pollutant emission potential when firing ammonia and ammonia blends. Chemical kinetic modeling of ammonia and its blends plays a crucial role in understanding combustion behavior and pollutant emissions, particularly for NOx. However, there are challenges in predicting NOx emissions accurately, with significant disparities among different models. High-fidelity numerical simulations using detailed and skeletal mechanisms, direct numerical simulation, and large eddy simulation, have helped uncover crucial operational conditions affecting combustion and pollutant emissions, such as combustor pressure, air dilution, wall cooling, fuel/air mixing, and fuel blending. Nonetheless, the accuracy of chemical kinetic models and their integration into turbulent flow simulations remain critical limitations for numerical simulations of ammonia combustion.

与传统的碳氢化合物燃料相比,氨作为一种燃料面临着巨大的挑战,包括点火能量高、反应活性低、火焰传播速度慢以及氮氧化物排放量高,这些都阻碍了氨作为可再生燃料的使用。将氨与天然气等化石燃料混合可提高其燃烧反应性,并有助于减少二氧化碳排放。然而,关于氨及其与碳氢化合物混合的复杂动力学,仍有许多问题需要了解。诸如反应动力学机制、点火特性、火焰传播行为以及在各种条件下控制燃烧性能的方法等关键领域都需要进一步阐明。本文回顾了近期在实验和数值模拟方面取得的进展,这些进展旨在开发稳定、低排放的燃氨发电燃烧器。本文分析了最近的燃烧器和火焰配置,包括非漩涡喷射燃烧器、单级漩涡燃烧器、双级燃烧器和新开发的双漩涡燃烧器,以了解它们在燃烧氨和氨混合物时的火焰稳定性和污染物排放潜力。氨及其混合物的化学动力学模型在了解燃烧行为和污染物排放(尤其是氮氧化物)方面起着至关重要的作用。然而,在准确预测氮氧化物排放方面存在挑战,不同模型之间存在显著差异。使用详细和骨架机制、直接数值模拟和大涡流模拟进行高保真数值模拟,有助于发现影响燃烧和污染物排放的关键运行条件,如燃烧器压力、空气稀释、壁面冷却、燃料/空气混合和燃料混合。尽管如此,化学动力学模型的准确性及其与湍流模拟的整合仍是氨燃烧数值模拟的关键限制因素。
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引用次数: 0
Turbulent partially cracked ammonia/air premixed spherical flames 湍流部分裂解氨/空气预混合球形火焰
Pub Date : 2024-06-17 DOI: 10.1016/j.jfueco.2024.100126
S. Zitouni, P. Bréquigny, C. Mounaïm-Rousselle

The combustion of ammonia requires, for most energy conversion systems, a combustion promoter such as hydrogen to guarantee the start-up, stability and combustion efficiency. Partially cracked ammonia (PCA) can provide sufficient hydrogen concentrations to enhance the burning velocity in comparison with pure ammonia. However, little work exists on the use of PCA blends operating under relevant turbulent conditions. To that end the outwardly propagating spherical flame configuration was employed to determine the laminar and turbulent flame propagation characteristics of PCA (NH3/(H2+N2)) and corresponding binary (NH3/H2) mixtures across various turbulent combustion regimes. First, PCA and ammonia-hydrogen blends exhibit similar flame propagation rates under various turbulent intensities, even for the laminar case. The highest turbulent burning velocity was observed at leanest conditions, as opposed to laminar flames which exhibited highest flame speed at conditions above stoichiometry. Under rich conditions, no substantial flame enhancement due to turbulence was measured irrespective of the hydrogen content. This lack of flame enhancement under turbulent conditions is attributed to the effect of preferential diffusion with good agreement observed with trends in measured Markstein numbers. The normalized turbulent flame speed is dominated by the enhanced molecular diffusivity afforded by the presence of hydrogen up to 15 % enrichment, prior to decreasing upon further hydrogen addition under lean and stoichiometric conditions. This ‘bending’ phenomenon may be the contribution of several factors including; the transitioning between combustion regimes associated with low Damköhler numbers (Da) and flame thickening; merging of flamelets due to the presence of ammonia enhancing wrinkling; and combined changes in laminar burning velocity and preferential diffusional behavior. Furthermore, good agreement for turbulent flame speed is observed with a correlation that includes the influence of turbulent stretch (Ka) and non-equidiffusion (Le), with the agreement reducing with decreasing chemical to turbulent time scale ratios (Da << 1).

对于大多数能量转换系统而言,氨的燃烧需要氢气等燃烧促进剂,以保证启动、稳定性和燃烧效率。与纯氨相比,部分裂解氨(PCA)可以提供足够浓度的氢气来提高燃烧速度。然而,在相关湍流条件下使用 PCA 混合物的研究却很少。为此,我们采用了向外传播的球形火焰构型,以确定 PCA(NH3/(H2+N2))和相应的二元(NH3/H2)混合物在各种湍流燃烧条件下的层流和湍流火焰传播特性。首先,在不同的湍流强度下,PCA 和氨氢混合物的火焰传播速度相似,甚至在层流情况下也是如此。在最贫油的条件下,湍流燃烧速度最高,而层流火焰在高于化学计量的条件下火焰速度最高。在富氢条件下,无论氢含量多少,都没有测得湍流导致的火焰大幅增强。湍流条件下火焰没有增强的原因是优先扩散的影响,这与测量的马克斯坦数的趋势非常吻合。归一化的湍流火焰速度主要是由于氢的存在提高了分子扩散率,最高可达 15%,而在贫氢和化学计量条件下,进一步添加氢后,湍流火焰速度会降低。这种 "弯曲 "现象可能是多种因素共同作用的结果,其中包括:与低达姆克勒数(Da)和火焰增粗相关的燃烧状态之间的转换;由于氨的存在而导致的小火焰合并,从而增强了皱纹;以及层流燃烧速度和优先扩散行为的综合变化。此外,湍流火焰速度与包含湍流伸展(Ka)和非液体扩散(Le)影响的相关性也有很好的一致性,一致性随着化学与湍流时间尺度比(Da <<1)的降低而降低。
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引用次数: 0
Advancing sustainable urban mobility: insights from best practices and case studies 推进可持续城市交通:最佳做法和案例研究的启示
Pub Date : 2024-06-08 DOI: 10.1016/j.jfueco.2024.100125
Dimitrios Minas Papadakis, Andreas Savvides, Aimilios Michael, Apostolos Michopoulos

Cities continue to expand along with the growth of population, while our mobility systems often fail to meet the demands for social, environmental and economic sustainability. The second industrial revolution enabled the extensive use of private vehicles, posing various challenges to the sustainability of such systems. Luckily, several best practices aiming at tackling this issue have been identified in the past, facilitating progress towards sustainability. Nowadays, this progress is strongly supported by the call for cities to develop Sustainable Mobility Plans (SUMPS), which stands as an opportunity for best practices to be implemented in coordination with relevant policies. This research identifies the best practices that promote a modal shift, while it investigates their alignment with the strategy that enhances public transport services, encourages active mobility and disincentivizes private vehicle usage. Therefore, the presentation of these practices, introduces a set of initiatives that under aforementioned strategy promotes a modal shift. Furthermore, through the identification of best practices in various locations, several insights and inferences are drawn, providing useful guidance.

随着人口的增长,城市不断扩大,而我们的交通系统却往往无法满足社会、环境和经济可持续发展的要求。第二次工业革命促成了私人车辆的广泛使用,给此类系统的可持续性带来了各种挑战。幸运的是,过去已经确定了一些旨在解决这一问题的最佳做法,推动了可持续发展的进程。如今,城市制定可持续交通计划(SUMPS)的号召有力地支持了这一进展,这为最佳实践与相关政策协调实施提供了机会。本研究确定了促进交通模式转变的最佳做法,同时还调查了这些做法与加强公共交通服务、鼓励积极交通、抑制私家车使用的战略是否一致。因此,在介绍这些做法时,介绍了根据上述战略促进交通模式转变的一系列举措。此外,通过确定各地的最佳做法,还得出了一些见解和推论,提供了有益的指导。
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引用次数: 0
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Fuel Communications
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