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

机译:光谱学研究负责第1类/第2类混合CO2吸收剂优异稳定性的机理:第4类新类别

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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.
机译:混合1级/ 2级负载的胺CO2吸附剂在实际蒸汽条件下表现出优异的性能,但它们的胺固定和稳定机理尚不清楚。揭示造成吸附剂强大功能的相互作用对于进一步改进至关重要,并且可以促进实际应用。我们采用固态Si-29 CP-MAS和2-D FSLG H-1-C-13 CP HETCOR NMR光谱仪来探测氨基硅烷/二氧化硅,聚胺[聚(乙烯亚胺),PEI] /二氧化硅和杂化氨基硅烷/ PEI /二氧化硅吸附剂。一种独特的顺序浸渍吸附剂制备方法是在漫反射红外傅里叶变换光谱(DRIFTS)装置中执行的,以使胺二氧化硅界面处的胺键合机理与本体胺层中的胺键合机理脱钩。这些机理与每种吸附剂对加速液体H2O和TGA蒸汽处理(H2O稳定性)和氧化降解(热稳定性)的抵抗力有关。在对N-(3-(三甲氧基甲硅烷基)丙基)乙二胺(TMPED)/ PEI和(3-氨基丙基)三甲氧基硅烷(APTMS)/ PEI杂化物进行H2O测试后,高百分比的CO2捕获保留(PCR)和有机含量保留(OCR)值吸附剂与在氧化降解过程中观察到的胺类物质的协同稳定作用有关(热重分析-差示扫描量热法,TGA-DSC)。固态NMR光谱显示TMPED / PEI混合物的协同作用通过氢键键接的PEI NH2中心点中心点中心点NH2 TMPED和PEI NH2 HO Si / O Si-O(TMPED,T-2 )吸附剂内的连接。 DRIFTS进一步确定,PEI利用H键连接,将TMPED接枝到二氧化硅上,并且PEI分散在本体中稳定的聚合TMPED网络中。这些发现为建立氨基硅烷/聚胺/二氧化硅杂化吸附剂的4类类别提供了科学依据。

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