Journal of CO2 Utilization二氧化碳利用杂志

Journal of CO2 Utilization(英文缩写 J CO2 UTIL),ISSN 2212-9820,eISSN 2212-9839,中文译名:二氧化碳利用杂志 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
8.600
JCR 分区
Q1
CAS 分区
B2
近一年发文量
1
本站 PubMed 收录统计

发文量统计区间:2025-11-01 至 2026-10-31,按本站收录文献的发表日期统计。

ISSN: 2212-9820 · eISSN: 2212-9839 · 缩写: J CO2 UTIL ·中文: 二氧化碳利用杂志

期刊介绍

选择期刊介绍栏目

期刊简介

《Journal of CO2 Utilization》是一本聚焦二氧化碳资源化利用的国际期刊,涵盖化学、材料、能源与环境工程等交叉领域。主要发表将CO2转化为燃料、化学品、聚合物及矿物的原创研究,同时关注碳捕集与利用集成系统、生命周期评价及技术经济分析。读者群包括从事碳减排、催化、电化学和过程工程的研究人员与工程师。

研究方向

主要方向包括CO2催化转化(热催化、电催化、光催化)、CO2作为原料合成高附加值化学品与燃料、矿化固定、以及相关反应器与过程设计。论文类型以原创研究为主,兼有综述、短讯和观点文章,强调实验与理论结合,鼓励展示技术可行性与环境效益。

期刊特色

研究取向偏重应用基础与工程验证,要求数据扎实、机理清晰,并体现CO2利用的实际潜力。论文通常包含性能评价、稳定性测试和初步放大分析。适合催化、材料、化工、能源及环境领域的研究生、博士后和工业研发人员阅读,尤其适合关注碳循环技术的学者。

投稿难度

投稿难度中等偏上,对创新性、数据完整性和工程相关性要求较高。建议在投稿前明确CO2转化路径的新颖性,补充对照实验与稳定性数据,并讨论技术经济或环境意义。若仅报道常规催化剂性能而缺乏机理或应用深度,可能难以通过初审。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
20218.321Q1
20227.700Q1
20237.200Q1
20248.400Q1
20258.600Q1

Journal of CO2 Utilization 最新收录文献

  1. JCR分区: Q1 CAS分区: B2 影响因子: 8.6

    1. {"_":"CO to chemicals: evaluating the potential of Fischer-Tropsch naphthas as a circular source of light olefins.","sub":["2"]}

    作者:
    Anas Jamil Abdulrahman, Niko Heikkinen, Miia Nevander, Miloš Auersvald, Sphurti Prakash Kulkarni, Oleksii Mynko, Behzad Parvizi, Daniël Withoeck, Marco Huotari, Juha Lehtonen, Christian Frilund, Matti Reinikainen, Eveliina Mäkelä, Marvin Kusenberg, Kevin M Van Geem
    日期:
    2026-08-31

    Rising industrial CO₂ emissions and the limited capacity of current abatement technologies highlight the need for scalable carbon utilization pathways. Fischer-Tropsch synthesis provides a route to convert captured CO₂ into hydrocarbon feedstocks compatible with existing petrochemical processes, such as steam cracking. However, their suitability as steam cracker feedstocks has not yet been fully demonstrated. Three Fischer-Tropsch (FT)-derived feedstocks were generated from captured CO₂ via Reverse Water-Gas Shift followed by Fischer-Tropsch synthesis. The crude FT oil (i) was hydrotreated to produce hydrotreated FT oil (ii), and subsequent distillation yielded a hydrotreated FT naphtha (iii). The feedstocks were characterized using comprehensive two-dimensional gas chromatography, benchmarked against fossil naphtha in a bench-scale steam cracker, and evaluated for their impact on the carbon intensity of ethylene production. FT-derived feedstocks were highly paraffinic and contained negligible sulfur, nitrogen, halogens, and metals. Crude FT oil contained 11.7 wt% oxygenates and 11.3 wt% olefins, which were removed by hydrotreatment, yielding more stable steam cracker feedstocks. When steam-cracking the respective oils at 880 °C, the crude FT oil produced 38% more ethylene than fossil naphtha, while the yield of pyrolysis fuel oil (C) was halved. Further upgrading to hydrotreated FT naphtha increased the ethylene advantage to 48% and reduced pyrolysis fuel oil formation to one-third of that with fossil naphtha. The higher ethylene selectivity led to a 27% reduction in cracker-level CO₂ intensity compared with fossil naphtha. These results demonstrate that CO-derived FT feedstocks can serve as clean, high-yield alternatives for light olefin production within existing petrochemical infrastructure.

  2. JCR分区: Q1 CAS分区: B2 影响因子: 8.6

    2. {"_":"Management of surgical mask waste to activated carbons for CO capture.","sub":["2"]}

    作者:
    Jarosław Serafin, Joanna Sreńscek-Nazzal, Adrianna Kamińska, Oliwia Paszkiewicz, Beata Michalkiewicz
    日期:
    2022-03-13

    The worldwide COVID-19 pandemic has resulted in a huge amount of face masks being used up and thrown away, resulting in increased environmental pollution and infection risks. In our work, we have developed a highly efficient process of neutralizing face mask waste into a useful carbon material. Then, the prepared activated carbon was used for CO adsorption studies. A series of activated carbons from face masks used as a precursor were synthesized using KOH and the activation temperature was in the range of 600-800 °C. All materials were characterized by well-developed porosity. The influence of activation temperature on the textural properties of prepared activated carbons and their adsorption abilities were investigated. The highest CO adsorption was received for the M_800 carbon and it was 3.91 mmol/g at the temperature of 0 °C and the pressure of 1 bar. M_800 carbon exhibited also high selectivity of CO over N. Seven equilibrium isotherms were applied to the experimental data to find out the best fit (Langmuir, Freundlich, Sips, Toth, Unilan, Fritz-Schlunder and Radke-Prausnitz isotherms). The presented research provides an environmentally friendly and cost-effective method of recycling waste masks into a valuable product in the form of carbon and its potential use in the absorption of harmful CO influencing the greenhouse effect.

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