化工进展 ›› 2024, Vol. 43 ›› Issue (4): 2031-2048.DOI: 10.16085/j.issn.1000-6613.2023-0606
• 资源与环境化工 • 上一篇
廖昌建1(), 张可伟2, 王晶1, 曾翔宇1, 金平1, 刘志禹1
收稿日期:
2023-04-14
修回日期:
2023-06-16
出版日期:
2024-04-15
发布日期:
2024-05-13
通讯作者:
廖昌建
作者简介:
廖昌建(1984—),男,硕士,研究员,研究方向为碳捕集技术开发。E-mail:liaochangjian.fshy@sinopec.com。
基金资助:
LIAO Changjian1(), ZHANG Kewei2, WANG Jing1, ZENG Xiangyu1, JIN Ping1, LIU Zhiyu1
Received:
2023-04-14
Revised:
2023-06-16
Online:
2024-04-15
Published:
2024-05-13
Contact:
LIAO Changjian
摘要:
直接空气捕集(DAC)二氧化碳技术作为负碳排放技术的一种,可助力实现“双碳”目标,是一项极具发展前景的碳捕集技术。本文简述了DAC的发展历史与现有DAC项目的运行及发展情况,介绍了碱性氢氧化物溶液、胺溶液、氨基酸盐溶液/BIGs与碱度浓度变化四种液体DAC技术,以及固体碱(土)金属、固态胺、金属有机框架MOFs材料及变湿吸附等固体DAC技术。对各种DAC技术的工艺流程及相关设备进行了综述,详述了各种DAC技术的原理、二氧化碳捕集方法及吸附/吸收剂再生方式,重点分析了每种DAC技术在吸附/吸收剂性能、再生温度、再生能耗及循环稳定性等方面的优缺点。指出需进一步研发低成本、高吸附/吸收性能且循环稳定性好的DAC吸附/吸收剂,优化或开发吸附/吸收剂再生工艺,同时开发适用于DAC技术的过程强化技术,为DAC的后续规模化与商业化应用奠定基础。
中图分类号:
廖昌建, 张可伟, 王晶, 曾翔宇, 金平, 刘志禹. 直接空气捕集二氧化碳技术研究进展[J]. 化工进展, 2024, 43(4): 2031-2048.
LIAO Changjian, ZHANG Kewei, WANG Jing, ZENG Xiangyu, JIN Ping, LIU Zhiyu. Progress on direct air capture of carbon dioxide[J]. Chemical Industry and Engineering Progress, 2024, 43(4): 2031-2048.
所属公司 | 地点 | CO2储存或利用 | 起始时间 /年 | CO2捕集量/t∙a-1 |
---|---|---|---|---|
Global Thermostat | 美国 | 未知 | 2010 | 500 |
Global Thermostat | 美国 | 未知 | 2013 | 1000 |
Climeworks | 德国 | 利用 | 2015 | 1 |
Carbon Engineering | 加拿大 | 利用 | 2015 | 365 |
Climeworks | 瑞士 | 利用 | 2016 | 50 |
Climeworks | 瑞士 | 利用 | 2017 | 900 |
Climeworks | 冰岛 | 储存 | 2017 | 50 |
Climeworks | 瑞士 | 利用 | 2018 | 600 |
Climeworks | 瑞士 | 利用 | 2018 | 3 |
Climeworks | 意大利 | 利用 | 2018 | 150 |
Climeworks | 德国 | 利用 | 2019 | 3 |
Climeworks | 荷兰 | 利用 | 2019 | 3 |
Climeworks | 德国 | 利用 | 2019 | 3 |
Climeworks | 德国 | 利用 | 2019 | 50 |
Climeworks | 德国 | 利用 | 2020 | 50 |
Climeworks | 德国 | 利用 | 2020 | 3 |
Climeworks | 德国 | 利用 | 2020 | 3 |
Climeworks | 冰岛 | 储存 | 2021 | 4000 |
表1 全球现行DAC工厂[19]
所属公司 | 地点 | CO2储存或利用 | 起始时间 /年 | CO2捕集量/t∙a-1 |
---|---|---|---|---|
Global Thermostat | 美国 | 未知 | 2010 | 500 |
Global Thermostat | 美国 | 未知 | 2013 | 1000 |
Climeworks | 德国 | 利用 | 2015 | 1 |
Carbon Engineering | 加拿大 | 利用 | 2015 | 365 |
Climeworks | 瑞士 | 利用 | 2016 | 50 |
Climeworks | 瑞士 | 利用 | 2017 | 900 |
Climeworks | 冰岛 | 储存 | 2017 | 50 |
Climeworks | 瑞士 | 利用 | 2018 | 600 |
Climeworks | 瑞士 | 利用 | 2018 | 3 |
Climeworks | 意大利 | 利用 | 2018 | 150 |
Climeworks | 德国 | 利用 | 2019 | 3 |
Climeworks | 荷兰 | 利用 | 2019 | 3 |
Climeworks | 德国 | 利用 | 2019 | 3 |
Climeworks | 德国 | 利用 | 2019 | 50 |
Climeworks | 德国 | 利用 | 2020 | 50 |
Climeworks | 德国 | 利用 | 2020 | 3 |
Climeworks | 德国 | 利用 | 2020 | 3 |
Climeworks | 冰岛 | 储存 | 2021 | 4000 |
载体 | 胺基 | 实验环境 | 最大吸附容量 /mmol∙g-1 | 吸附-脱附 循环条件 | 循环吸附量 /mmol∙g-1 | 参考文献 |
---|---|---|---|---|---|---|
SBA-15 | TEPA(质量分数50%) | 400μg/g CO2 | 2.30(600min) | 吸附25℃, 60min; 脱附110℃, 15min | 1.72~1.66(10次循环) | [ |
大孔硅 | PA(10.98mmol /g) | 400μg/g CO2 | 2.65 | 10%CO2:吸附50℃,40min; 脱附110℃,10min | 3.86~3.78(120次循环) | [ |
介孔炭 | PEI(质量分数55%) | 400μg/g CO2 | 2.25(720min) | 吸附25℃;脱附110℃,45min | 2.25~2.18(10次循环) | [ |
多壁碳纳米管(NWCN) | PEI(质量分数20%乙醇) | 350μg/g CO2 | 2.12(720min) | 吸附30℃,10min;脱附90℃,20min | 1.07~0.96(10次循环) | [ |
纳米纤维(NFC) | AEAPDMS (4.9mmol/g) | 506μg/g CO2, RH40% | 1.39(720min) | 吸附25℃,120min; 脱附90℃,60min | 平均0.695(20次循环) | [ |
Mg0.55Al-CO3LDHs | TEPA(质量分数67%) | 400μg/g CO2 | 3.0(180min) | 吸附25℃,100min; 脱附100℃,10min | 1.31~1.19(80次循环) | [ |
Mg0.55Al-CO3LDHs | TEPA(质量分数67%) | 400μg/g CO2 | 3.0(180min) | 吸附25℃, 180min; 脱附100℃,15min | 2.55~2.31(20次循环) | [ |
Mg0.55Al-CO3LDHs | TRI(6.399mmol∙g-1) | 400μg/g CO2 | 1.05(120min) | 吸附25℃, 60min; 脱附120℃,15min | 0.912(50次循环) | [ |
层状SiO2 | TEPA(质量分数70%) | 400μg/g CO2 | 5.2(700min) | 吸附30℃,25min; 脱附110℃,30min | 4.5~3.5(10次循环) | [ |
Mg2(dobdc) | N2H4(6.01mmol∙g-1) | 400μg/g CO2 | 3.89 | 15%CO2:吸附40℃,40min; 脱附130℃ | 3.86(5次循环) | [ |
聚丙烯腈(PAN) 中空纤维 | TEPA(质量分数30.1%) | 470μg/g CO2, RH25% | 2.15(440min) | 吸附25℃;脱附100℃ | 2.03(20次循环) | [ |
表2 用于直接空气捕集的部分固态胺吸附剂研究结果
载体 | 胺基 | 实验环境 | 最大吸附容量 /mmol∙g-1 | 吸附-脱附 循环条件 | 循环吸附量 /mmol∙g-1 | 参考文献 |
---|---|---|---|---|---|---|
SBA-15 | TEPA(质量分数50%) | 400μg/g CO2 | 2.30(600min) | 吸附25℃, 60min; 脱附110℃, 15min | 1.72~1.66(10次循环) | [ |
大孔硅 | PA(10.98mmol /g) | 400μg/g CO2 | 2.65 | 10%CO2:吸附50℃,40min; 脱附110℃,10min | 3.86~3.78(120次循环) | [ |
介孔炭 | PEI(质量分数55%) | 400μg/g CO2 | 2.25(720min) | 吸附25℃;脱附110℃,45min | 2.25~2.18(10次循环) | [ |
多壁碳纳米管(NWCN) | PEI(质量分数20%乙醇) | 350μg/g CO2 | 2.12(720min) | 吸附30℃,10min;脱附90℃,20min | 1.07~0.96(10次循环) | [ |
纳米纤维(NFC) | AEAPDMS (4.9mmol/g) | 506μg/g CO2, RH40% | 1.39(720min) | 吸附25℃,120min; 脱附90℃,60min | 平均0.695(20次循环) | [ |
Mg0.55Al-CO3LDHs | TEPA(质量分数67%) | 400μg/g CO2 | 3.0(180min) | 吸附25℃,100min; 脱附100℃,10min | 1.31~1.19(80次循环) | [ |
Mg0.55Al-CO3LDHs | TEPA(质量分数67%) | 400μg/g CO2 | 3.0(180min) | 吸附25℃, 180min; 脱附100℃,15min | 2.55~2.31(20次循环) | [ |
Mg0.55Al-CO3LDHs | TRI(6.399mmol∙g-1) | 400μg/g CO2 | 1.05(120min) | 吸附25℃, 60min; 脱附120℃,15min | 0.912(50次循环) | [ |
层状SiO2 | TEPA(质量分数70%) | 400μg/g CO2 | 5.2(700min) | 吸附30℃,25min; 脱附110℃,30min | 4.5~3.5(10次循环) | [ |
Mg2(dobdc) | N2H4(6.01mmol∙g-1) | 400μg/g CO2 | 3.89 | 15%CO2:吸附40℃,40min; 脱附130℃ | 3.86(5次循环) | [ |
聚丙烯腈(PAN) 中空纤维 | TEPA(质量分数30.1%) | 470μg/g CO2, RH25% | 2.15(440min) | 吸附25℃;脱附100℃ | 2.03(20次循环) | [ |
技术名称 | 优点 | 缺点 |
---|---|---|
碱性氢氧化物溶液DAC技术 | 技术成熟,吸收速率高 | 再生温度高、再生能耗高,损失大量水分 |
胺溶液DAC技术 | 吸收速率较高 | 伴随胺液挥发且再生效率较低 |
氨基酸盐溶液/BIGs DAC技术 | 吸收速率高,再生温度较低,溶剂损失少 | 能耗较高,捕集效果因BIGs 而异 |
碱度浓度变化DAC技术 | 吸收速率较高,再生温度与能耗较低,可与海水淡化研究合作 | 捕集效果与溶液浓缩技术相关联,用水量大 |
固体碱(土)金属DAC技术 | 吸附效率较高,再生稳定性较好 | 再生能耗较高,成本较高 |
固态胺吸附剂DAC技术 | 技术成熟,吸附速率快,再生温度低 | 吸附剂的热稳定性有待进一步提高 |
MOFs材料DAC技术 | 在较低温度下有应用优势 | 捕集效果受环境中水含量影响较大,原材料成本较高 |
变湿吸附DAC技术 | 吸附与解吸速率高,再生温度及再生能耗较低 | 用水量大,对水质要求高,得到的CO2分压较低 |
DACM技术 | 可同时实现CO2捕集与转化,受湿度影响较小 | 再生温度较高,催化剂起决定性作用 |
光诱导摆动吸附DAC技术 | 再生能耗较低 | 需在材料内嵌入光反应因子 |
MI-DAC技术 | 再生能耗较低,可应用于海水 | 捕集效果主要取决于微生物 |
表3 各种DAC技术对比
技术名称 | 优点 | 缺点 |
---|---|---|
碱性氢氧化物溶液DAC技术 | 技术成熟,吸收速率高 | 再生温度高、再生能耗高,损失大量水分 |
胺溶液DAC技术 | 吸收速率较高 | 伴随胺液挥发且再生效率较低 |
氨基酸盐溶液/BIGs DAC技术 | 吸收速率高,再生温度较低,溶剂损失少 | 能耗较高,捕集效果因BIGs 而异 |
碱度浓度变化DAC技术 | 吸收速率较高,再生温度与能耗较低,可与海水淡化研究合作 | 捕集效果与溶液浓缩技术相关联,用水量大 |
固体碱(土)金属DAC技术 | 吸附效率较高,再生稳定性较好 | 再生能耗较高,成本较高 |
固态胺吸附剂DAC技术 | 技术成熟,吸附速率快,再生温度低 | 吸附剂的热稳定性有待进一步提高 |
MOFs材料DAC技术 | 在较低温度下有应用优势 | 捕集效果受环境中水含量影响较大,原材料成本较高 |
变湿吸附DAC技术 | 吸附与解吸速率高,再生温度及再生能耗较低 | 用水量大,对水质要求高,得到的CO2分压较低 |
DACM技术 | 可同时实现CO2捕集与转化,受湿度影响较小 | 再生温度较高,催化剂起决定性作用 |
光诱导摆动吸附DAC技术 | 再生能耗较低 | 需在材料内嵌入光反应因子 |
MI-DAC技术 | 再生能耗较低,可应用于海水 | 捕集效果主要取决于微生物 |
捕集能力 | 吸附剂/吸收剂 | 解吸温度/℃ | 能源 | 能耗 | CO2压力/bar | CO2纯度 | 成本/USD·t-1 | 参考文献 |
---|---|---|---|---|---|---|---|---|
1Mt/a | KOH | 900 | 天然气 | 8.81GJ/t | 150 | 97.1% | 94~232 | [ |
1Mt/a | KOH | 900 | 天然气+电力 | 5.25GJ/t+366kWh/t | 150 | 97.1% | 94~232 | [ |
1Mt/a | KOH | 900 | 电力 | 1535kWh/t | 1 | >97% | 186 | [ |
0.291t/h | MEA | 123.1 | 电力 | 1452kWh/t | 2 | — | 676 | [ |
0.36Mt/a | K2CO3 | 80~100 | 余热 | 7.5GJ/t+694kWh/t | — | >99% | 135~177 | [ |
3600t/a | K2CO3 | 80~100 | 余热 | 7.5GJ/t+694kWh/t | — | >99% | 203~244 | [ |
— | CaO | 875 | 太阳能 | 240.9 GJ/t | — | — | — | [ |
— | K2CO3/γ-Al2O3 | 150 | 热能+机械能 | 7.3GJ/t+0.27GJ/t | — | — | — | [ |
300t/a | 胺基 | 100 | 余热 | 5.4~7.2GJ/t+200~300Wh/t | — | 99.9% | 预计大规模75 | [ |
— | 氨基聚合物 | 85~95 | 蒸汽 | 4.2~5.1GJ/t+150~260Wh/t | — | >98.5% | <113 | [ |
— | 氨基聚合物 | 75 | 低温蒸汽 | — | — | >98.5% | ≤50 | [ |
140g/d | MOFs | 80,真空 | 余热 | — | — | 70%~80% | 34~350 | [ |
166.08t/h | 变湿吸附剂+胺液 | — | 太阳能 | 306GJ/t | — | 97% | 93.1 | [ |
365t/a | 变湿吸附剂 | 变湿 | 电力 | 316kWh/t | — | — | 99 (预期<30) | [ |
— | 变湿吸附剂 | 45 | 余热 | 0.81GJ/t | — | 3% | 34.68 | [ |
— | 氨基酸盐溶液/m-BBIG | 60~120 | 余热 | 8.2GJ/t | — | — | — | [ |
— | 氨基酸盐溶液/PyBIG | 80~120 | 余热 | 6.5GJ/t | — | — | — | [ |
— | ACS | RO | 电力 | 1011~1200kWh/t | 1 | 99.8% | — | [ |
— | ACS | MCDI | 电力 | 1072~2400kWh/t | 1 | 99.8% | — | [ |
1Mt/a | MI-DAC | pH改变 | 生物能 | — | — | — | 30.54 | [ |
表4 DAC技术能耗及成本比较
捕集能力 | 吸附剂/吸收剂 | 解吸温度/℃ | 能源 | 能耗 | CO2压力/bar | CO2纯度 | 成本/USD·t-1 | 参考文献 |
---|---|---|---|---|---|---|---|---|
1Mt/a | KOH | 900 | 天然气 | 8.81GJ/t | 150 | 97.1% | 94~232 | [ |
1Mt/a | KOH | 900 | 天然气+电力 | 5.25GJ/t+366kWh/t | 150 | 97.1% | 94~232 | [ |
1Mt/a | KOH | 900 | 电力 | 1535kWh/t | 1 | >97% | 186 | [ |
0.291t/h | MEA | 123.1 | 电力 | 1452kWh/t | 2 | — | 676 | [ |
0.36Mt/a | K2CO3 | 80~100 | 余热 | 7.5GJ/t+694kWh/t | — | >99% | 135~177 | [ |
3600t/a | K2CO3 | 80~100 | 余热 | 7.5GJ/t+694kWh/t | — | >99% | 203~244 | [ |
— | CaO | 875 | 太阳能 | 240.9 GJ/t | — | — | — | [ |
— | K2CO3/γ-Al2O3 | 150 | 热能+机械能 | 7.3GJ/t+0.27GJ/t | — | — | — | [ |
300t/a | 胺基 | 100 | 余热 | 5.4~7.2GJ/t+200~300Wh/t | — | 99.9% | 预计大规模75 | [ |
— | 氨基聚合物 | 85~95 | 蒸汽 | 4.2~5.1GJ/t+150~260Wh/t | — | >98.5% | <113 | [ |
— | 氨基聚合物 | 75 | 低温蒸汽 | — | — | >98.5% | ≤50 | [ |
140g/d | MOFs | 80,真空 | 余热 | — | — | 70%~80% | 34~350 | [ |
166.08t/h | 变湿吸附剂+胺液 | — | 太阳能 | 306GJ/t | — | 97% | 93.1 | [ |
365t/a | 变湿吸附剂 | 变湿 | 电力 | 316kWh/t | — | — | 99 (预期<30) | [ |
— | 变湿吸附剂 | 45 | 余热 | 0.81GJ/t | — | 3% | 34.68 | [ |
— | 氨基酸盐溶液/m-BBIG | 60~120 | 余热 | 8.2GJ/t | — | — | — | [ |
— | 氨基酸盐溶液/PyBIG | 80~120 | 余热 | 6.5GJ/t | — | — | — | [ |
— | ACS | RO | 电力 | 1011~1200kWh/t | 1 | 99.8% | — | [ |
— | ACS | MCDI | 电力 | 1072~2400kWh/t | 1 | 99.8% | — | [ |
1Mt/a | MI-DAC | pH改变 | 生物能 | — | — | — | 30.54 | [ |
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