Demonstration of CO2 Capture Process Monitoring and Solvent Degradation Detection by Chemometrics at the Technology Centre Mongstad CO2 Capture Plant

被引:1
|
作者
Wagaarachchige, Jayangi D. [1 ]
Idris, Zulkifli [2 ]
Khatibzadeh, Ayandeh [1 ]
Drageset, Audun [3 ]
Jens, Klaus-J. [2 ]
Halstensen, Maths [1 ]
机构
[1] Univ South Eastern Norway, Dept Elect IT & Cybernet, N-3918 Porsgrunn, Norway
[2] Univ South Eastern Norway, Dept Proc Energy & Environm Technol, N-3918 Porsgrunn, Norway
[3] Technol Ctr Mongstad TCM DA, N-5954 Mongstad, Norway
关键词
PILOT-PLANT; ABSORPTION; SPECIATION; AMINES;
D O I
10.1021/acs.iecr.3c00134
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Solvent managementis one of the important current challenges inpost combustion carbon capture (PCC) technology development. Usinglarge-scale 1960 h test campaign data (Technology Centre Mongstad,Norway, 2015 MEA Test), we demonstrate a combination of multivariatemethods (PLS-R, MSPC) and process analytical spectroscopy (FT-IR)as a tool to monitor and control PCC process performance. Two MEAsolvent monitoring models, total inorganic carbon (TIC) content andtotal alkalinity (TA), were prepared. In long-term solvent monitoring,PLS-R model prediction uncertainty increased due to gradual solventchanges, e.g., solvent degradation and impurity accumulation. Hence,we show a specific model update methodology to keep the models updated,leading to good long-term monitoring ability of the TIC and TA models.In addition to reliable long-term solvent monitoring ability, a newprinciple for follow-up of thermal solvent reclaiming was demonstrated.This shows that the need for solvent reclaiming can be quantified.Furthermore, this methodology is an indicator to see the actual solventdeviation from the fresh solvent. This quantification may providean input for "start" and "end of reclaiming operation"identification. Hence, we demonstrate that it is possible to extractinformation for process performance follow-up, solvent monitoring,and solvent reclaiming from a single spectroscopic instrument.
引用
收藏
页码:9747 / 9754
页数:8
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