{"title":"表面活性剂在室温下辅助合成均相钙基CO2吸附剂","authors":"C. Y. Foo, A. Mohamed, Keat-Teong Lee, D. Irvan","doi":"10.6000/1929-5030.2014.03.03.6","DOIUrl":null,"url":null,"abstract":"Calcium oxide (CaO) sorbents have been recently used for removal of CO 2 gases in fossil fuel-fired power plant. However, there are some limitations of CaO in CO 2 capturing such as rapid loss of activity during the capture cycles, which is a result of sintering, attrition, and consequent elutriation. Therefore, this paper has demonstrated a novel synthesis method to produce CaO at room temperature to avoid abovementioned drawbacks. In addition, introduction of ionic surfactant of sodium dodecyl sulfate to the CaO formation solution has shown a positive result of formation of homogeneous spherical particle with a mean Z-average diameter of 345.2 nm and polydispersion index (PDI) of 0.335 by dynamical light scattering measurement. Subjected to a high calcination temperature of 1200 o C, developed CaO is able to maintain a CO 2 uptake capacity of 0.1025 g CO2 /g sorbent under 30 minutes of carbonation time. Despite its lower CO 2 uptake capacity compared to maximum theoretical limit of 0.78 g CO2/gsorbent , CaO particles is able to withstand a high calcination temperature of 1200 o C and reported a particle size distribution ranged from 0.4 - 1.2µm after calcination which is just slightly larger than fresh developed CaO. Given that such small narrow distributed size of CaO, developed CaO at room temperature is good for packed-bed reactor in calcium looping processes and more studies are required to find a suitable support for fluidized bed reactor type. This successful synthesis story of CaO particle at room temperature has unraveled the possibility to develop nanosized CaO at room temperature in order to achieve high CO 2 uptake capacity while enjoying its superior thermal stability over multiple carbonation/calcination cycles.","PeriodicalId":15165,"journal":{"name":"Journal of Applied Solution Chemistry and Modeling","volume":"32 1","pages":"175-185"},"PeriodicalIF":0.0000,"publicationDate":"2014-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Surfactant Assisted Synthesis of Homogeneous Calcium Based CO2 Sorbent at Room Temperature\",\"authors\":\"C. Y. Foo, A. Mohamed, Keat-Teong Lee, D. Irvan\",\"doi\":\"10.6000/1929-5030.2014.03.03.6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Calcium oxide (CaO) sorbents have been recently used for removal of CO 2 gases in fossil fuel-fired power plant. However, there are some limitations of CaO in CO 2 capturing such as rapid loss of activity during the capture cycles, which is a result of sintering, attrition, and consequent elutriation. Therefore, this paper has demonstrated a novel synthesis method to produce CaO at room temperature to avoid abovementioned drawbacks. In addition, introduction of ionic surfactant of sodium dodecyl sulfate to the CaO formation solution has shown a positive result of formation of homogeneous spherical particle with a mean Z-average diameter of 345.2 nm and polydispersion index (PDI) of 0.335 by dynamical light scattering measurement. Subjected to a high calcination temperature of 1200 o C, developed CaO is able to maintain a CO 2 uptake capacity of 0.1025 g CO2 /g sorbent under 30 minutes of carbonation time. Despite its lower CO 2 uptake capacity compared to maximum theoretical limit of 0.78 g CO2/gsorbent , CaO particles is able to withstand a high calcination temperature of 1200 o C and reported a particle size distribution ranged from 0.4 - 1.2µm after calcination which is just slightly larger than fresh developed CaO. Given that such small narrow distributed size of CaO, developed CaO at room temperature is good for packed-bed reactor in calcium looping processes and more studies are required to find a suitable support for fluidized bed reactor type. This successful synthesis story of CaO particle at room temperature has unraveled the possibility to develop nanosized CaO at room temperature in order to achieve high CO 2 uptake capacity while enjoying its superior thermal stability over multiple carbonation/calcination cycles.\",\"PeriodicalId\":15165,\"journal\":{\"name\":\"Journal of Applied Solution Chemistry and Modeling\",\"volume\":\"32 1\",\"pages\":\"175-185\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Applied Solution Chemistry and Modeling\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.6000/1929-5030.2014.03.03.6\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Solution Chemistry and Modeling","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6000/1929-5030.2014.03.03.6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
近年来,氧化钙(CaO)吸附剂被广泛应用于燃煤电厂的co2脱除。然而,CaO在co2捕获中存在一些局限性,例如在捕获周期中活性的快速损失,这是烧结,磨损和随后的洗脱的结果。因此,本文展示了一种在室温下合成CaO的新方法,以避免上述缺点。此外,将离子表面活性剂十二烷基硫酸钠引入到CaO形成溶液中,通过动态光散射测量,形成了平均z -平均直径为345.2 nm,多色散指数(PDI)为0.335的均匀球形颗粒。经过1200℃的高温煅烧,焙烧后的CaO在30分钟的碳化时间内仍能保持0.1025 g CO2 /g吸附剂的CO2吸收量。尽管CaO颗粒的CO2吸收能力低于理论上限0.78 g CO2/吸附剂,但CaO颗粒能够承受1200℃的高温,煅烧后的粒径分布范围为0.4 - 1.2µm,仅略大于新开发的CaO。由于CaO的分布尺寸小且窄,在室温条件下制备的CaO有利于填充床反应器的钙环化工艺,需要更多的研究来寻找合适的流化床反应器类型的载体。这个在室温下成功合成CaO颗粒的故事,揭示了在室温下开发纳米级CaO的可能性,以获得高的CO 2吸收能力,同时在多次碳化/煅烧循环中享有优越的热稳定性。
Surfactant Assisted Synthesis of Homogeneous Calcium Based CO2 Sorbent at Room Temperature
Calcium oxide (CaO) sorbents have been recently used for removal of CO 2 gases in fossil fuel-fired power plant. However, there are some limitations of CaO in CO 2 capturing such as rapid loss of activity during the capture cycles, which is a result of sintering, attrition, and consequent elutriation. Therefore, this paper has demonstrated a novel synthesis method to produce CaO at room temperature to avoid abovementioned drawbacks. In addition, introduction of ionic surfactant of sodium dodecyl sulfate to the CaO formation solution has shown a positive result of formation of homogeneous spherical particle with a mean Z-average diameter of 345.2 nm and polydispersion index (PDI) of 0.335 by dynamical light scattering measurement. Subjected to a high calcination temperature of 1200 o C, developed CaO is able to maintain a CO 2 uptake capacity of 0.1025 g CO2 /g sorbent under 30 minutes of carbonation time. Despite its lower CO 2 uptake capacity compared to maximum theoretical limit of 0.78 g CO2/gsorbent , CaO particles is able to withstand a high calcination temperature of 1200 o C and reported a particle size distribution ranged from 0.4 - 1.2µm after calcination which is just slightly larger than fresh developed CaO. Given that such small narrow distributed size of CaO, developed CaO at room temperature is good for packed-bed reactor in calcium looping processes and more studies are required to find a suitable support for fluidized bed reactor type. This successful synthesis story of CaO particle at room temperature has unraveled the possibility to develop nanosized CaO at room temperature in order to achieve high CO 2 uptake capacity while enjoying its superior thermal stability over multiple carbonation/calcination cycles.