基于蒙斯塔德技术中心腐蚀监测结果的MEA水溶液CO2吸收工艺材料选择评估

N. Flø, Leila Faramarzi, F. Iversen, Eirik Romslo Kleppe, Brit Graver, Heidi Nornes Bryntesen, K. Johnsen
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引用次数: 6

摘要

2017年和2018年,蒙斯塔德技术中心(TCM)通过一系列测试活动,对单乙醇胺(MEA)水溶液捕集CO2进行了长期测试。作为测试活动的一部分,通过对材料测试券的调查和分析,对CO2-MEA过程的材料选择进行了评估。测试板在工厂的五个不同位置暴露在不同的操作条件下。金属和橡胶材料都进行了测试,以检测二氧化碳- mea工艺中可能存在的材料兼容性问题。除CS235外,所有金属都被证明是合适的,CS235暴露在MEA溶剂中通常表现出严重的腐蚀速率。然而,一项中期失重分析表明,CS235在冷富溶剂位置的特定工艺条件下可能是可以接受的。测试的橡胶材料没有明显的变化,但硬度和拉伸性能的微小变化表明受到MEA溶剂环境的影响。除了检查试样外,还经常监测溶剂中可能指示或影响腐蚀的典型因素,如溶解金属和热稳定盐(HSS)的浓度。在具体操作阶段之间观察到平均金属溶解度存在一些差异,但是,烟气源似乎对金属溶解度没有显著影响。
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Assessment of Material Selection for the CO2 Absorption Process with Aqueous MEA Solution Based on Results from Corrosion Monitoring at Technology Centre Mongstad
Abstract In 2017 and 2018, Technology Centre Mongstad (TCM) performed long-term testing of CO2 capture with aqueous monoethanolamine (MEA) solvent through a series of test campaigns. As part of the test campaigns, a selection of materials was assessed for the CO2-MEA process by investigation and analysis of material test coupons. The test coupons were exposed to various operating conditions at five different locations in the plant. Both metal and rubber materials were tested in order to detect possible material compatibility issues with the CO2-MEA process. All metals proved to be suitable, except CS235 which in general showed severe corrosion rates exposed to the MEA solvent. However, a mid-campaign weight loss analysis indicated that CS235 might be acceptable for specific process conditions on the cold rich solvent location. No significant changes were observed on the tested rubber materials, however minor changes in hardness and tensile properties indicated some impact by the MEA solvent environment. In addition to examination of test coupons, the solvent was frequently monitored for typical factors that might indicate or influence corrosion such as the concentration of dissolved metals and heat stable salts (HSS). Some variability in average metal dissolution was observed between specific operational phases, however, the flue gas source did not seem to have significant effect on metal dissolution.
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