Rock ‘n’ use of CO2: carbon footprint of carbon capture and utilization by mineralization
Literature Information
Hesam Ostovari, André Sternberg
A recent approach to reduce the carbon footprint of industries with process-inherent CO2 emissions is CO2 mineralization. Mineralization stores CO2 by converting it into a thermodynamically stable solid. Beyond storing CO2, the products of CO2 mineralization can potentially substitute conventional products in several industries. Substituting conventional production increases both the economic and the environmental potential of carbon capture and utilization (CCU) by mineralization. The promising potential of CO2 mineralization is, however, challenged by the high energy demand required to overcome the slow reaction kinetics. To provide a sound assessment of the climate impacts of CCU by mineralization, we determine the carbon footprint of CCU by mineralization based on life cycle assessment. For this purpose, we analyze 7 pathways proposed in literature: 5 direct and 2 indirect mineralization pathways, considering serpentine, olivine, and steel slag as feedstock. The mineralization products are employed to partially substitute cement in blended cement. Our results show that all considered CCU technologies for mineralization could reduce climate impacts over the entire life cycle based on the current state-of-the-art and today's energy mix. Reductions range from 0.44 to 1.17 ton CO2e per ton CO2 stored. To estimate an upper bound on the potential of CCU by mineralization, we consider an ideal-mineralization scenario that neglects all process inefficiencies and utilizes the entire product. For this ideal mineralization, mineralization of 1 ton CO2 could even avoid up to 3.2 times more greenhouse gas emissions than only storing CO2. For all mineralization pathways, the carbon footprint is mainly reduced due to the permanent storage of CO2 and the credit for substituting conventional products. Thus, developing suitable products is critical to realize the potential benefits in practice. Then, carbon capture and utilization by mineralization could provide a promising route for climate change mitigation.
Related Literature
Macroscopic and local approaches of phase transition in sol–gel synthesized (Bi0.5Na0.5)TiO3–SrTiO3 thin films
Hyun-Young Lee, Jin Luo, Zhen Zhou, Wei Sun, Jing-Feng Li
DOI: 10.1039/C8CP01830H
Enhanced fluorescence of phthalimide compounds induced by the incorporation of electron-donating alicyclic amino groups
Ryoji Orita, Marius Franckevičius, Aurimas Vyšniauskas, Vidmantas Gulbinas, Haruki Sugiyama, Hidehiro Uekusa, Kenta Kanosue, Ryohei Ishige, Shinji Ando
DOI: 10.1039/C8CP01999A
Li+-Induced fluorescent metallogel: a case of ESIPT-CHEF and ICT phenomenon
Manish Kumar Dixit, Mrigendra Dubey
DOI: 10.1039/C8CP04579H
Computational study of the carbonyl–ene reaction between formaldehyde and propylene encapsulated in coordinatively unsaturated metal–organic frameworks M3(btc)2 (M = Fe, Co, Ni, Cu and Zn)
Thana Maihom, Michael Probst, Jumras Limtrakul
DOI: 10.1039/C8CP06841K
Electron correlation effects of the ThO and ThS molecules in the spinor basis. A relativistic coupled cluster study of ground and excited states properties
Paweł Tecmer, Cristina E. González-Espinoza
DOI: 10.1039/C8CP00048D
Most favorable cumulenic structures in iron-capped linear carbon chains are short singlet odd-carbon dications: a theoretical view
Liang Pu, Zhong Zhang, R. Bruce King, Wesley D. Allen
DOI: 10.1039/C7CP08673C
Tuning the photoreactivity of Z-hexatriene photoswitches by substituents – a non-adiabatic molecular dynamics study
Enrico Tapavicza, Travis Thompson, Kenneth Redd, Dan Kim
DOI: 10.1039/C8CP05181J
Pure spin current and phonon thermoelectric transport in a triangulene-based molecular junction
Jianwei Li, Yihang Nie, Fuming Xu, Yunjin Yu, Bin Wang
DOI: 10.1039/C8CP02322K
Theoretical study on photophysical properties of three high water solubility polypyridyl complexes for two-photon photodynamic therapy
Ying-Tao Liu, Xue Yin, Xiao-Yong Lai, Xin Wang
DOI: 10.1039/C8CP01069B
Detection of simple inorganic and organic molecules over Cu-decorated circumcoronene: a combined DFT and QTAIM study
Lukáš Bučinský, Filipe Teixeira, M. Natália D. S. Cordeiro
DOI: 10.1039/C8CP02035C
You might also like
Is 2-(2-chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) safe?
2-(2-Chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) is generally consi...
Is 2-(Benzyloxy)-5-bromobenzoic acid (CAS: 62176-31-2) safe?
2-(Benzyloxy)-5-bromobenzoic acid can be handled safely if appropriate precautio...
What is (4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride (CAS: 1159825-48-5)?
(4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride is a chemical compound ...
What is 2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54-7)?
2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54...
Are there alternatives to 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS: 102771-26-6) in synthesis?
While 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS:...
What is the market or research trend for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine-6-carboxylate (CAS: 851376-80-2)?
The market for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine...
How should waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) be handled?
Waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) should ...
How is (6-Fluoro-3-pyridinyl)boronic acid (CAS: 351019-18-6) typically synthesized?
(6-Fluoro-3-pyridinyl)boronic acid can be synthesized through the reaction of 6-...
What industries use Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9)?
Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9) finds applications in vario...
What is the market or research trend for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4)?
The market for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4) is g...















![2-(5-Bromo-1H-pyrrolo[2,3-B]pyridin-3-YL)acetic acid structure 2-(5-Bromo-1H-pyrrolo[2,3-B]pyridin-3-YL)acetic acid structure](https://static.chemtradehub.com/structs/106/1060795-03-0-0589.webp)