Bio-inspired mineralization of CO2 into CaCO3: Single-step carbon capture and utilization with controlled crystallization

矿化(土壤科学) 结晶 碳酸钙 化学工程 三乙醇胺 球霰石 碳酸盐 碳酸铵 化学 无机化学 氮气 有机化学 分析化学(期刊) 文石 工程类
作者
Dharmjeet Madhav,Bart Buffel,Frederik Desplentere,Paula Moldenaers,Veerle Vandeginste
出处
期刊:Fuel [Elsevier BV]
卷期号:345: 128157-128157 被引量:23
标识
DOI:10.1016/j.fuel.2023.128157
摘要

CO2 mineralization which involves the reaction of CO2 with alkaline earth metal cations to form carbonates, is a promising pathway that could be crucial for combating global warming via long-term CO2 utilization and storage. However, due to the large abundance of natural calcium carbonate (CaCO3) and advanced milling techniques, micron-ranged CaCO3 is conventionally produced via the top-down method because it is more economically attractive than mineralization or precipitation unless particles with functional properties are generated so that a higher product value is achieved. In this study, inspired by the natural formation of nacre, which is produced naturally via controlled crystallization (using environmental CO2) in the marine environment, we produce CaCO3 particles with different morphologies via single-step CO2 capture and mineralization. We used a gas diffuser reaction setup to bubble CO2 in liquid media containing CO2 absorption promotor, water-soluble polymer, and surfactant as crystal growth modifiers, and Ca2+ to form functional CaCO3. First, different inorganic and organic CO2 absorption promoters and their combinations were investigated for their effectiveness on Ca2+ conversion to CaCO3. Ca2+ conversion and pH of the reaction system with various concentrations of CO2 absorption promoters were monitored every 5 min. Second, the effect of the polymer combined with different concentrations of surfactant on CaCO3 properties was studied. It was found that the combination of triethanolamine and ammonium hydroxide as absorption promotors results in 53.2% Ca2+ conversion into stable CaCO3 particles within 5 min of CO2 bubbling. Absorption promotors themselves could not regulate the particle shape; however, with increasing concentrations, smaller particles agglomerated to form bigger rhombohedral particles. Polymer and surfactant-mediated mineralization of CO2 produces spherical and hollow, stable calcite particles that could serve as dies, heavy metal adsorbents, supports to catalysts, functional composite fillers, etc.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
刚刚
SBQHY完成签到,获得积分10
刚刚
hm发布了新的文献求助10
刚刚
雪妮儿完成签到,获得积分10
1秒前
ZQ完成签到,获得积分10
2秒前
jing1012发布了新的文献求助10
2秒前
西柚完成签到,获得积分10
2秒前
博修发布了新的文献求助10
2秒前
健康的朋友完成签到,获得积分10
3秒前
3秒前
snf发布了新的文献求助10
3秒前
蓦然发布了新的文献求助10
3秒前
123发布了新的文献求助10
3秒前
CY完成签到,获得积分10
4秒前
4秒前
危险人物完成签到,获得积分10
4秒前
善良飞丹完成签到,获得积分10
4秒前
余杭村王小虎完成签到,获得积分10
5秒前
JISOO发布了新的文献求助30
5秒前
尔玉完成签到,获得积分10
6秒前
王老吉完成签到,获得积分10
6秒前
香蕉招牌完成签到,获得积分10
6秒前
清茶发布了新的文献求助10
6秒前
深情安青应助Lion采纳,获得10
6秒前
7秒前
TTTT完成签到,获得积分10
8秒前
邓志天完成签到,获得积分10
8秒前
8秒前
8秒前
8秒前
诸岩完成签到,获得积分10
9秒前
zhangzhang1145完成签到,获得积分10
9秒前
Gauss应助小诸葛采纳,获得30
10秒前
10秒前
10秒前
10秒前
11秒前
Yu完成签到,获得积分10
12秒前
xxx完成签到 ,获得积分10
12秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Manipulating the Mouse Embryo: A Laboratory Manual, Fourth Edition 1000
INQUIRY-BASED PEDAGOGY TO SUPPORT STEM LEARNING AND 21ST CENTURY SKILLS: PREPARING NEW TEACHERS TO IMPLEMENT PROJECT AND PROBLEM-BASED LEARNING 500
Founding Fathers The Shaping of America 500
Distinct Aggregation Behaviors and Rheological Responses of Two Terminally Functionalized Polyisoprenes with Different Quadruple Hydrogen Bonding Motifs 460
Writing to the Rhythm of Labor Cultural Politics of the Chinese Revolution, 1942–1976 300
Lightning Wires: The Telegraph and China's Technological Modernization, 1860-1890 250
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 催化作用 遗传学 冶金 电极 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 4571800
求助须知:如何正确求助?哪些是违规求助? 3992744
关于积分的说明 12359771
捐赠科研通 3665912
什么是DOI,文献DOI怎么找? 2020329
邀请新用户注册赠送积分活动 1054614
科研通“疑难数据库(出版商)”最低求助积分说明 942138