Gad Licht , Ethan Peltier , Simon Gee , Stuart Licht
{"title":"Eliminating active CO2 concentration in Carbon Capture and Storage (CCUS): Molten carbonate decarbonization through an insulation/diffusion membrane","authors":"Gad Licht , Ethan Peltier , Simon Gee , Stuart Licht","doi":"10.1016/j.decarb.2024.100094","DOIUrl":null,"url":null,"abstract":"<div><div>Present industrial decarbonization technologies require an active CO<sub>2</sub>-concentration system, often based on lime reaction or amine binding reactions, which is energy intensive and carries a high CO<sub>2</sub>-footprint. Here instead, an effective process without active CO<sub>2</sub> concentration is demonstrated in a new process-termed IC2CNT (Insulation-diffusion facilitated CO<sub>2</sub> to Carbon Nanomaterial Technology) decarbonization process. Molten carbonates such as Li<sub>2</sub>CO<sub>3</sub> (mp 723 °C) are highly insoluble to industrial feed gas principal components (N<sub>2</sub>, O<sub>2</sub>, and H<sub>2</sub>O). However, CO<sub>2</sub> can readily dissolve and react in molten carbonates. We have recently characterized high CO<sub>2</sub> diffusion rates through porous aluminosilicate and calcium-magnesium silicate thermal insulations. Here, the CO<sub>2</sub> in ambient feed gas passes through these membranes into molten Li<sub>2</sub>CO<sub>3</sub>. The membrane also concurrently insulates the feed gas from the hot molten carbonate chamber, obviating the need to heat the (non-CO<sub>2</sub>) majority of the feed gas to high temperature. In this insulation facilitated decarbonization process CO<sub>2</sub> is split by electrolysis in the molten carbonate producing sequestered, high-purity carbon nanomaterials (such as CNTs) and O<sub>2</sub>.</div></div>","PeriodicalId":100356,"journal":{"name":"DeCarbon","volume":"7 ","pages":"Article 100094"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"DeCarbon","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294988132400060X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Present industrial decarbonization technologies require an active CO2-concentration system, often based on lime reaction or amine binding reactions, which is energy intensive and carries a high CO2-footprint. Here instead, an effective process without active CO2 concentration is demonstrated in a new process-termed IC2CNT (Insulation-diffusion facilitated CO2 to Carbon Nanomaterial Technology) decarbonization process. Molten carbonates such as Li2CO3 (mp 723 °C) are highly insoluble to industrial feed gas principal components (N2, O2, and H2O). However, CO2 can readily dissolve and react in molten carbonates. We have recently characterized high CO2 diffusion rates through porous aluminosilicate and calcium-magnesium silicate thermal insulations. Here, the CO2 in ambient feed gas passes through these membranes into molten Li2CO3. The membrane also concurrently insulates the feed gas from the hot molten carbonate chamber, obviating the need to heat the (non-CO2) majority of the feed gas to high temperature. In this insulation facilitated decarbonization process CO2 is split by electrolysis in the molten carbonate producing sequestered, high-purity carbon nanomaterials (such as CNTs) and O2.