{"title":"Solution loss behavior of cokes and its kinetics under hydrogen-enriched atmosphere","authors":"Jingchong YAN, Kaixiang MA, Rong GE, Zhiping LEI, Zhanku LI, Weidong ZHANG, Shibiao REN, Zhicai WANG, Hengfu SHUI","doi":"10.1016/S1872-5813(25)60532-9","DOIUrl":null,"url":null,"abstract":"<div><div>Hydrogen-enriched ironmaking presents a promising approach to mitigate coke consumption and carbon emission in blast furnace (BF) operations. This work investigated the relationship between the structural features of cokes and their reactivity towards solution loss (SL), especially under hydrogen-enriched atmospheres. Six cokes were characterized, and their SL behaviors were examined under varying atmospheres to elucidate the effects of hydrogen enrichment. The results indicate that an increase in fixed carbon content leads to a decrease in the coke reactivity index (CRI) and an increase in coke strength after reaction (CSR), in the CO<sub>2</sub> atmosphere, the CSR of coke increases from 35.76%−62.83%, while in the 90CO<sub>2</sub>/10H<sub>2</sub> atmosphere, the CSR of coke increases from 65.67%−84.09%. There is a good linear relationship between CRI and microcrystalline structure parameters of coke. Cokes with larger crystalline size, lower amorphous content, and smaller optical texture index (OTI) values show enhanced resistance to degradation and maintain structural integrity in BF. Kinetic analysis performed with the shifted-modified-random pore model (S-MRPM) reveals that alterations in pore structure and intrinsic mineral composition significantly influence the reaction rate. The introduction of a small amount of water vapor raises SL rates, whereas a minor addition of hydrogen (<10%) decelerates SL due to its incomplete conversion to water vapor and the reduced partial pressure of the gasifying agent. Thermodynamic calculations also indicate that the introduced hydrogen does not convert into the same fraction of water vapor. The shift from chemical reaction control to gas diffusion control as the rate-determining step with rising temperatures during SL process was confirmed, and the introduction of hydrogen does not notably alter SL behavior. This result demonstrated that introducing a small amount of hydrogen (<10%) can mitigate SL rates, thereby enhancing coke strength and reducing coke consumption and carbon emissions.</div></div>","PeriodicalId":15956,"journal":{"name":"燃料化学学报","volume":"53 7","pages":"Pages 1123-1136"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"燃料化学学报","FirstCategoryId":"1087","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872581325605329","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0
Abstract
Hydrogen-enriched ironmaking presents a promising approach to mitigate coke consumption and carbon emission in blast furnace (BF) operations. This work investigated the relationship between the structural features of cokes and their reactivity towards solution loss (SL), especially under hydrogen-enriched atmospheres. Six cokes were characterized, and their SL behaviors were examined under varying atmospheres to elucidate the effects of hydrogen enrichment. The results indicate that an increase in fixed carbon content leads to a decrease in the coke reactivity index (CRI) and an increase in coke strength after reaction (CSR), in the CO2 atmosphere, the CSR of coke increases from 35.76%−62.83%, while in the 90CO2/10H2 atmosphere, the CSR of coke increases from 65.67%−84.09%. There is a good linear relationship between CRI and microcrystalline structure parameters of coke. Cokes with larger crystalline size, lower amorphous content, and smaller optical texture index (OTI) values show enhanced resistance to degradation and maintain structural integrity in BF. Kinetic analysis performed with the shifted-modified-random pore model (S-MRPM) reveals that alterations in pore structure and intrinsic mineral composition significantly influence the reaction rate. The introduction of a small amount of water vapor raises SL rates, whereas a minor addition of hydrogen (<10%) decelerates SL due to its incomplete conversion to water vapor and the reduced partial pressure of the gasifying agent. Thermodynamic calculations also indicate that the introduced hydrogen does not convert into the same fraction of water vapor. The shift from chemical reaction control to gas diffusion control as the rate-determining step with rising temperatures during SL process was confirmed, and the introduction of hydrogen does not notably alter SL behavior. This result demonstrated that introducing a small amount of hydrogen (<10%) can mitigate SL rates, thereby enhancing coke strength and reducing coke consumption and carbon emissions.
期刊介绍:
Journal of Fuel Chemistry and Technology (Ranliao Huaxue Xuebao) is a Chinese Academy of Sciences(CAS) journal started in 1956, sponsored by the Chinese Chemical Society and the Institute of Coal Chemistry, Chinese Academy of Sciences(CAS). The journal is published bimonthly by Science Press in China and widely distributed in about 20 countries. Journal of Fuel Chemistry and Technology publishes reports of both basic and applied research in the chemistry and chemical engineering of many energy sources, including that involved in the nature, processing and utilization of coal, petroleum, oil shale, natural gas, biomass and synfuels, as well as related subjects of increasing interest such as C1 chemistry, pollutions control and new catalytic materials. Types of publications include original research articles, short communications, research notes and reviews. Both domestic and international contributors are welcome. Manuscripts written in Chinese or English will be accepted. Additional English titles, abstracts and key words should be included in Chinese manuscripts. All manuscripts are subject to critical review by the editorial committee, which is composed of about 10 foreign and 50 Chinese experts in fuel science. Journal of Fuel Chemistry and Technology has been a source of primary research work in fuel chemistry as a Chinese core scientific periodical.