Spectroscopic Investigation of the Mechanisms Responsible for the Superior Stability of Hybrid Class 1/Class 2 CO2 Sorbents: A New Class 4 Category

被引:49
|
作者
Wilfong, Walter Christopher [1 ,2 ]
Kail, Brian W. [3 ]
Jones, Christopher W. [5 ]
Pacheco, Carlos [4 ]
Gray, McMahan L. [1 ]
机构
[1] US DOE, Natl Energy Technol Lab, 626 Cochrans Mill Rd, Pittsburgh, PA 15236 USA
[2] Oak Ridge Natl Lab, POB 2008, Oak Ridge, TN 37831 USA
[3] AECOM, 626 Cochrans Mill Rd, Pittsburgh, PA 15236 USA
[4] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[5] Georgia Inst Technol, Sch Chem & Biomol Engn, 311 Ferst Dr, Atlanta, GA 30332 USA
关键词
CO2; capture; hybrid; Class; 4; amine sorbent; infrared spectroscopy; NMR; CARBON-DIOXIDE CAPTURE; HOLLOW-FIBER SORBENTS; SILICA-GEL; AMINE SORBENTS; ADSORBED CO2; SUPPORTED POLYETHYLENIMINE; OXIDATIVE-DEGRADATION; ADSORPTION; PERFORMANCE; SORPTION;
D O I
10.1021/acsami.6b02062
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Hybrid Class 1/Class 2 supported amine CO2 sorbents demonstrate superior performance under practical steam conditions, yet their amine immobilization and stabilization mechanisms are unclear. Uncovering the interactions responsible for the sorbents' robust features is critical for further improvements and can facilitate practical applications. We employ solid state Si-29 CP-MAS and 2-D FSLG H-1-C-13 CP HETCOR NMR spectroscopies to probe the overall molecular interactions of aminosilane/silica, polyamine [poly(ethylenimine), PEI]/silica, and hybrid aminosilane/PEI/silica sorbents. A unique, sequential impregnation sorbent preparation method is executed in a diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) setup to decouple amine binding mechanisms at the amine silica interfacefrom those within bulk amine layers. These mechanisms are correlated with each sorbents' resistance to accelerated liquid H2O and TGA steam treatments (H2O stability) and to oxidative degradation (thermal stability). High percentages of CO2 capture retained (PCR) and organic content retained (OCR) values after H2O testing of N-(3-(trimethoxysilyl)propyl)ethylenediamine (TMPED)/PEI and (3-aminopropyl)trimethoxysilane (APTMS)/PEI hybrid sorbents are associated with a synergistic stabilizing effect of the amine species observed during oxidative degradation (thermal gravimetric analysis-differential scanning calorimetry, TGA-DSC). Solid state NMR spectroscopy reveals that the synergistic effect of the TMPED/PEI mixture is manifested by the formation of hydrogen-bonded PEI NH2 center dot center dot center dot NH2 TMPED and PEI NH2 HO Si/O Si-O (TMPED, T-2) linkages within the sorbent. DRIFTS further determines that PEI enhances the grafting of TMPED to silica and that PEI is dispersed among a stable network of polymerized TMPED in the bulk, utilizing H-bonded linkages. These findings provide the scientific basis for establishing a Class 4 category for aminosilane/polyamine/silica hybrid sorbents.
引用
收藏
页码:12780 / 12791
页数:12
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