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Nitrogen-functionalized modulation of iron nanoparticles promotes selective hydrogenation of carbon dioxide 铁纳米颗粒的氮功能化调制促进了二氧化碳的选择性氢化
Green Carbon Pub Date : 2025-03-01 Epub Date: 2025-01-07 DOI: 10.1016/j.greenca.2024.09.010
Xianbiao Wang , Jun Qian , Zixuan Lu , Jie Huang , Liru Zheng , Yong Jiang , Mengdie Cai , Yuxue Wei , Lisheng Guo , Song Sun
{"title":"Nitrogen-functionalized modulation of iron nanoparticles promotes selective hydrogenation of carbon dioxide","authors":"Xianbiao Wang ,&nbsp;Jun Qian ,&nbsp;Zixuan Lu ,&nbsp;Jie Huang ,&nbsp;Liru Zheng ,&nbsp;Yong Jiang ,&nbsp;Mengdie Cai ,&nbsp;Yuxue Wei ,&nbsp;Lisheng Guo ,&nbsp;Song Sun","doi":"10.1016/j.greenca.2024.09.010","DOIUrl":"10.1016/j.greenca.2024.09.010","url":null,"abstract":"<div><div>Nitrogen-functionalized iron nanoparticles were prepared using a one-pot hydrothermal process. The utilization of urea as a nitrogen source during the hydrothermal process significantly influenced the morphology and defects of the obtained catalyst. Within an optimal range, the actual nitrogen promoter content could be controlled by altering the amount of urea introduced. The presence of a nitrogen promoter not only impacts catalytic activity but also plays a crucial role in product distribution. The FeC-N catalyst exhibited 32.0% selectivity toward light olefins, with a CO<sub>2</sub> conversion of 26.8%. The improvement in catalytic performance correlated with the specific surface area, dispersion of iron species, number of defect sites, and content of pyrrolic N species. Moreover, the enhanced selectivity for light olefins can be attributed to easier desorption from the FeC-N catalyst, thereby avoiding the over-hydrogenation of light olefins to paraffins.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"3 1","pages":"Pages 36-43"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724853","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
Rational design of H2 production sites for achieving photoconversion of CO2 with H2O into widely adjustable syngas and highly effective H2 evolution 合理设计产氢位点,实现CO2与H2O光转化为可广泛调节的合成气和高效的氢气析出
Green Carbon Pub Date : 2025-03-01 Epub Date: 2024-11-23 DOI: 10.1016/j.greenca.2024.07.008
Guoqiang Zhang , Zhiqi Wang , Diandian Shi , Guangbo Liu , Tao He , Jingli Wu , Jinzhi Zhang , Jinhu Wu
{"title":"Rational design of H2 production sites for achieving photoconversion of CO2 with H2O into widely adjustable syngas and highly effective H2 evolution","authors":"Guoqiang Zhang ,&nbsp;Zhiqi Wang ,&nbsp;Diandian Shi ,&nbsp;Guangbo Liu ,&nbsp;Tao He ,&nbsp;Jingli Wu ,&nbsp;Jinzhi Zhang ,&nbsp;Jinhu Wu","doi":"10.1016/j.greenca.2024.07.008","DOIUrl":"10.1016/j.greenca.2024.07.008","url":null,"abstract":"<div><div>The photoconversion of CO<sub>2</sub> with H<sub>2</sub>O into widely tunable syngas (CO and H<sub>2</sub>) or pure H<sub>2</sub> production is regarded as a promising strategy to mitigate escalating energy shortages and climate change. Herein, anchoring the H<sub>2</sub> production sites onto the surface of CdIn<sub>2</sub>S<sub>4</sub> (CIS) with a nanoscale hollow sphere allows for the photoconversion of CO<sub>2</sub> into syngas and water splitting to H<sub>2</sub>. The CO/H<sub>2</sub> ratio can be realized in a remarkably wide range from 1:0.38 to 1:3.76. The optimized CIS/Co-PBA/NaY-5 hybrid exhibits superior photocatalytic syngas evolution up to 1458.48 μmol·g<sup>−1</sup>·h<sup>−1</sup> (H<sub>2</sub>/CO, 1152.29/306.19 μmol·g<sup>−1</sup>·h<sup>−1</sup>), and the H<sub>2</sub> evolution rate increases by 431.70% compared with CIS. The CIS/Co-PBA/NaY-5 hybrid exhibited not only superior H<sub>2</sub> evolution but also recyclability. The experimental, energy-dispersive X-ray spectroscopy, and electron spin resonance results indicate that the Co sites serve as H<sub>2</sub> production sites and promote the H<sub>2</sub> evolution reaction. In addition, the construction of a p-n heterojunction with a special micromorphology is beneficial for the separation/transfer of carriers.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"3 1","pages":"Pages 11-21"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724851","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
Alcohol pretreatment for depolymerization and fractionation of corn stalk 玉米秸秆醇预处理解聚分馏研究
Green Carbon Pub Date : 2025-03-01 Epub Date: 2024-10-23 DOI: 10.1016/j.greenca.2024.09.005
Lijuan Gao , Wentao Li , Yu Zhang , Meijing Wang , Wen Wang , Cuiyi Liang , Shiyou Xing , Wei Qi
{"title":"Alcohol pretreatment for depolymerization and fractionation of corn stalk","authors":"Lijuan Gao ,&nbsp;Wentao Li ,&nbsp;Yu Zhang ,&nbsp;Meijing Wang ,&nbsp;Wen Wang ,&nbsp;Cuiyi Liang ,&nbsp;Shiyou Xing ,&nbsp;Wei Qi","doi":"10.1016/j.greenca.2024.09.005","DOIUrl":"10.1016/j.greenca.2024.09.005","url":null,"abstract":"<div><div>The development of an efficient pretreatment technology to depolymerize and fractionate lignocellulose into glucan, xylan, and lignin is crucial for lignocellulose biorefinery. In this study, alcohol pretreatments using methanol and pentanol were developed and compared. Based on the solubility of the two alcohols, the methanol and pentanol pretreatments are homogeneous and biphasic, respectively. Carbon flow analysis revealed that 1 kg of corn stalk (CS) yielded 111.9 g of lignin with the homogeneous pretreatment (lignin yield: 60.0%), while 149.8 g of lignin was obtained with the biphasic pretreatment (lignin yield: 80.3%). Biphasic pretreatment yielded the lignin with higher activity (more β-O-4 bond content). Additionally, 210.4 g and 267.0 g of glucose were obtained from the enzymatic hydrolysis of homogeneously and biphasically pretreated CS, respectively, where glucose yields were 53.0% and 67.2%, respectively. Fourier Transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) were employed to verify the component fractionation results. The Hansen solubility parameter and combined severity factor analysis were used to evaluate the effects of various factors on component fractionation. Nuclear magnetic resonance and mechanistic analyses were performed to explore the process of component fractionation. Overall, we discovered that biphasic pretreatment was significantly better than homogeneous pretreatment in component fractionation, including component recovery and lignin activity.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"3 1","pages":"Pages 100-109"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724849","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
Recent advances in microalgae-driven carbon capture, utilization, and storage: Strain engineering through adaptive laboratory evolution and microbiome optimization 微藻驱动的碳捕获、利用和储存的最新进展:通过适应性实验室进化和微生物组优化的菌株工程
Green Carbon Pub Date : 2025-03-01 Epub Date: 2024-11-09 DOI: 10.1016/j.greenca.2024.10.001
Zhongshi He , Jing Wang , Yantao Li
{"title":"Recent advances in microalgae-driven carbon capture, utilization, and storage: Strain engineering through adaptive laboratory evolution and microbiome optimization","authors":"Zhongshi He ,&nbsp;Jing Wang ,&nbsp;Yantao Li","doi":"10.1016/j.greenca.2024.10.001","DOIUrl":"10.1016/j.greenca.2024.10.001","url":null,"abstract":"<div><div>The potential of microalgae as a biological resource for carbon capture, utilization, and storage (CCUS) has been extensively discussed. Although genetic engineering methods have been employed to improve microalgal phenotypes, they often face challenges related to public concerns regarding genetically modified organisms. By contrast, adaptive laboratory evolution (ALE) and microbiome optimization have emerged as promising non-genetic modification strategies, with notable success in bacterial models. In microalgae, ALE has been employed to improve resilience against varying environmental and stress factors and increase carbon capture efficiency, and for the production of valuable bioproducts through gradual accumulation of beneficial mutations following manual or automated selection. Furthermore, advancements in the understanding of microbial symbiotic relationships in the phycosphere have facilitated microbiome optimization in microalgal cultivation systems, significantly improving their functionality and productivity. In this study, we provide a comprehensive overview of the latest advancements in ALE and microbiome optimization of microalgae for CCUS across different carbon emission scenarios, including flue gas, biogas, wastewater, and landfill leachate. We further discuss the current challenges and future directions for the integration of ALE with microbiome optimization, focusing on the potential synergies of these methodologies. Overall, ALE and microbiome optimization are promising approaches to direct microalgae for environmental and industrial CCUS applications, thereby reducing global carbon emissions and addressing climate change challenges.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"3 1","pages":"Pages 74-99"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724848","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
Direct synthesis of alkyl amines from dinitrogen and alkenes 二氮和烯烃直接合成烷基胺
Green Carbon Pub Date : 2025-03-01 Epub Date: 2024-08-31 DOI: 10.1016/j.greenca.2024.08.002
Jinhui Wang , Yanwei Cao , Cuijuan Zhang , Lin He , Jiaxiang Chu
{"title":"Direct synthesis of alkyl amines from dinitrogen and alkenes","authors":"Jinhui Wang ,&nbsp;Yanwei Cao ,&nbsp;Cuijuan Zhang ,&nbsp;Lin He ,&nbsp;Jiaxiang Chu","doi":"10.1016/j.greenca.2024.08.002","DOIUrl":"10.1016/j.greenca.2024.08.002","url":null,"abstract":"","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"3 1","pages":"Pages 44-45"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724854","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
Breaking the stability limit of zeolite-based alkane dehydrogenation catalysts 突破沸石基烷烃脱氢催化剂的稳定性极限
Green Carbon Pub Date : 2025-03-01 Epub Date: 2024-09-07 DOI: 10.1016/j.greenca.2024.07.006
Zhiqiang Liu , Anmin Zheng
{"title":"Breaking the stability limit of zeolite-based alkane dehydrogenation catalysts","authors":"Zhiqiang Liu ,&nbsp;Anmin Zheng","doi":"10.1016/j.greenca.2024.07.006","DOIUrl":"10.1016/j.greenca.2024.07.006","url":null,"abstract":"","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"3 1","pages":"Pages 46-47"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724321","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
Efficient atomically dispersed Fe catalysts with robust three-phase interface for stable seawater-based zinc-air batteries 具有坚固三相界面的高效原子分散铁催化剂用于稳定的海水基锌-空气电池
Green Carbon Pub Date : 2025-03-01 Epub Date: 2024-10-18 DOI: 10.1016/j.greenca.2024.09.002
Daokun Kang , Canhui Zhang , Xingkun Wang , Fanqi Wang , Huiyu Gai , Hanxu Yao , Xu Liu , Zhuangzhuang He , Minghua Huang , Heqing Jiang
{"title":"Efficient atomically dispersed Fe catalysts with robust three-phase interface for stable seawater-based zinc-air batteries","authors":"Daokun Kang ,&nbsp;Canhui Zhang ,&nbsp;Xingkun Wang ,&nbsp;Fanqi Wang ,&nbsp;Huiyu Gai ,&nbsp;Hanxu Yao ,&nbsp;Xu Liu ,&nbsp;Zhuangzhuang He ,&nbsp;Minghua Huang ,&nbsp;Heqing Jiang","doi":"10.1016/j.greenca.2024.09.002","DOIUrl":"10.1016/j.greenca.2024.09.002","url":null,"abstract":"<div><div>The use of seawater-based electrolytes in zinc-air batteries (S-ZABs) presents significant economic and social benefits and mitigates the demand for scarce freshwater resources. However, it is challenging to achieve a metal–nitrogen–carbon (M–N–C) catalyst that exhibits high resistance to corrosive Cl<sup>–</sup> in seawater-based electrolytes and possesses a strengthened binding affinity with O<sub>2</sub>, which enables catalysts with an optimized oxygen reduction reaction (ORR) and enhances the applicability of S-ZABs. Herein, we propose a combined wet chemistry-pyrolysis strategy to obtain atomically dispersed Fe-decorated nitrogen-doped mesoporous carbon spheres (N-MCS-Fe-900). Benefiting from the capacity of the Fe decorations to form the edge-hosted aerophilic FeN<sub>4</sub>-O<sub>2</sub> sites at the optimized three-phase interface, N-MCS-Fe-900 affords the enhanced resistance of the active Fe sites to corrosive Cl<sup>–</sup>, as well as improved interaction with O<sub>2</sub>, thereby facilitating the ORR process. As expected, the N-MCS-Fe-900 delivers high half wave potential of 0.90 V and kinetic current density of 18.61 mA cm<sup>−2</sup> at 0.85 V in seawater-based 0.1 M KOH. More importantly, the S-ZABs equipped with N-MCS-Fe-900 exhibited long-term stability under a high current density for over 140 h without voltage decay. Theoretical calculations and electrochemical performance evaluations collectively revealed the superior catalytic efficacy and genesis of this activity in N-MCS-Fe-900, which features edge-hosted FeN<sub>4</sub>-O<sub>2</sub> sites at the stable three-phase interface in seawater electrolytes. This study provides new insights for the advancement of ORR catalysts in sustainable energy conversion technologies for seawater-based electrolytes.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"3 1","pages":"Pages 1-10"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143724850","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
One-pot conversion of cellulosic sugars into methyl lactate using hierarchical Sn-MFI zeolite with intracrystalline mesoporosity 利用具有晶内介孔的分级Sn-MFI沸石一锅法将纤维素糖转化为乳酸甲酯
Green Carbon Pub Date : 2024-12-01 Epub Date: 2024-08-13 DOI: 10.1016/j.greenca.2024.06.007
Yuying Li , Xiumei Liu , Kun Zhang , Siyuan Zhao , Lei Wu , Qiang Guo , Hong Du , Feng Wang
{"title":"One-pot conversion of cellulosic sugars into methyl lactate using hierarchical Sn-MFI zeolite with intracrystalline mesoporosity","authors":"Yuying Li ,&nbsp;Xiumei Liu ,&nbsp;Kun Zhang ,&nbsp;Siyuan Zhao ,&nbsp;Lei Wu ,&nbsp;Qiang Guo ,&nbsp;Hong Du ,&nbsp;Feng Wang","doi":"10.1016/j.greenca.2024.06.007","DOIUrl":"10.1016/j.greenca.2024.06.007","url":null,"abstract":"<div><div>Cellulosic sugars derived from lignocellulose are the most abundant and inexpensive raw materials used for the production of methyl lactate (MLA). In this study, hierarchical Sn-MFI zeolite with intracrystalline mesoporosity was developed, capable of catalyzing the one-pot conversion of cellulosic sugars into MLA in a CH<sub>3</sub>OH/H<sub>2</sub>O mixture. The MLA yield from glucose using the hierarchical Sn-MFI zeolite was almost twice as high as that using the conventional microporous Sn-MFI zeolite. This superior catalytic performance was attributed to the reduced diffusion limitation of glucose within the hierarchical Sn-MFI catalyst, which possessed significant intercrystalline mesoporosity. Additionally, the hierarchical Sn-MFI catalyst was recycled for five reaction runs of the one-pot conversion of glucose without an obvious loss of activity, indicating excellent stability and reusability and broadening the scope of carbohydrates used to obtain MLA.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"2 4","pages":"Pages 383-392"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098286","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
Enhancing the performance of spinel La-doped CoFe2O4 oxygen carriers for chemical looping hydrogen generation 提高尖晶石la掺杂CoFe2O4氧载体化学环制氢性能
Green Carbon Pub Date : 2024-12-01 Epub Date: 2024-09-30 DOI: 10.1016/j.greenca.2024.08.004
Weifeng Song , Jingli Wu , Jianqing Li , Zhiqi Wang , Tao He , Wenqing Chen , Deshuai Sun , Jinhu Wu
{"title":"Enhancing the performance of spinel La-doped CoFe2O4 oxygen carriers for chemical looping hydrogen generation","authors":"Weifeng Song ,&nbsp;Jingli Wu ,&nbsp;Jianqing Li ,&nbsp;Zhiqi Wang ,&nbsp;Tao He ,&nbsp;Wenqing Chen ,&nbsp;Deshuai Sun ,&nbsp;Jinhu Wu","doi":"10.1016/j.greenca.2024.08.004","DOIUrl":"10.1016/j.greenca.2024.08.004","url":null,"abstract":"<div><div>Chemical-looping hydrogen generation (CLHG) is a clean and efficient method for sustainable hydrogen production. The industrial advancement of the CLHG technology hinges on the development of highly active and selective oxygen carriers (OCs). In this study, the performances of three spinel OCs (ZnFe<sub>2</sub>O<sub>4</sub>, CoFe<sub>2</sub>O<sub>4</sub>, and NiFe<sub>2</sub>O<sub>4</sub>) were investigated in a fixed-bed reactor. CoFe<sub>2</sub>O<sub>4</sub> demonstrated the best reactivity and highest hydrogen yield. In addition, doping CoFe<sub>2</sub>O<sub>4</sub> with varying amounts of La further improved its performance. The highest hydrogen yield (393 mL/g) was observed for CoFe<sub>2</sub>O<sub>4</sub> doped with 10% by mass of La. The characterization results indicated that La not only facilitated the formation of oxygen vacancies but also accelerated lattice oxygen transfer. Furthermore, an optimized La doping level was found to boost the crystallinity of the oxygen carrier, leading to improved cycling performance. The insights gained from probing the performance of La-doped CoFe<sub>2</sub>O<sub>4</sub> OCs are expected to contribute to the development of novel OCs for scaled-up CLHG technology.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"2 4","pages":"Pages 393-400"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143150009","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
Interdisciplinary results of an Italian research project on methane recovery and carbon dioxide storage in natural gas hydrate reservoirs 意大利关于天然气水合物储层中甲烷回收和二氧化碳储存的跨学科研究项目的成果
Green Carbon Pub Date : 2024-12-01 Epub Date: 2024-10-09 DOI: 10.1016/j.greenca.2024.09.001
Beatrice Castellani , Rita Giovannetti , Umberta Tinivella , Salvatore F. Cannone , Roberto Fazioli , Fabio Trippetta , Michele Ciulla , Valentino Canale , Pietro Di Profio , Alberto Maria Gambelli , Andrea Nicolini , Giorgio Minelli , Massimiliano Barchi , Marco Zannotti , Andrea Rossi , Michela Giustiniani , Andrea Lanzini , Massimo Santarelli , Federico Rossi
{"title":"Interdisciplinary results of an Italian research project on methane recovery and carbon dioxide storage in natural gas hydrate reservoirs","authors":"Beatrice Castellani ,&nbsp;Rita Giovannetti ,&nbsp;Umberta Tinivella ,&nbsp;Salvatore F. Cannone ,&nbsp;Roberto Fazioli ,&nbsp;Fabio Trippetta ,&nbsp;Michele Ciulla ,&nbsp;Valentino Canale ,&nbsp;Pietro Di Profio ,&nbsp;Alberto Maria Gambelli ,&nbsp;Andrea Nicolini ,&nbsp;Giorgio Minelli ,&nbsp;Massimiliano Barchi ,&nbsp;Marco Zannotti ,&nbsp;Andrea Rossi ,&nbsp;Michela Giustiniani ,&nbsp;Andrea Lanzini ,&nbsp;Massimo Santarelli ,&nbsp;Federico Rossi","doi":"10.1016/j.greenca.2024.09.001","DOIUrl":"10.1016/j.greenca.2024.09.001","url":null,"abstract":"<div><div>Natural gas hydrates (NGH) are found in marine sediments on continental and island slopes, deep-water sediments of inland lakes and seas, and polar sediments on continents and continental shelves. NGH constitutes the largest hydrocarbon resource on Earth, representing a reservoir of sustainable fuel owing to the possibility of a so-called CO<sub>2</sub>–CH<sub>4</sub> replacement process. If CO<sub>2</sub> is injected into NGH sediments, CH<sub>4</sub> is released and CO<sub>2</sub> hydrate formed. The extraction of gas from NGH, combined with carbon capture, presents significant potential advantages in the energy infrastructure and various economic and political contexts, aligning with future green policies. This study contributes to the advancement of knowledge by reviewing the findings of a three-year Italian research project focused on methane recovery and carbon dioxide disposal in NGH. The consortium comprises seven multidisciplinary Italian partners. This study introduces a novel process wherein the CO<sub>2</sub>–CH<sub>4</sub> replacement process is integrated with methane purification and CO<sub>2</sub> recirculation, which has been experimentally tested and represents a new advancement in gas hydrate science. Experimental tests at the microscopic and macroscopic levels showed that the efficiency of the process strongly depends on the mutual influence of the properties of water, sediment, and the involved gaseous species. Energy evaluations show that the ratio between the energy spent to complete an entire cycle of replacement and recirculation over the stored energy in the recovered methane is 17%, resulting in a beneficial energy balance, while economic analysis shows that the transition could generate—even in the short term—large high-impact cash-out.</div></div>","PeriodicalId":100595,"journal":{"name":"Green Carbon","volume":"2 4","pages":"Pages 351-365"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098284","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}
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