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用于增强二氧化碳吸附的纳米结构二氧化硅吸附剂经热碱处理后的最佳表面氨基功能化

Optimal Surface Amino-Functionalization Following Thermo-Alkaline Treatment of Nanostructured Silica Adsorbents for Enhanced CO₂ Adsorption.

作者信息

Medina-Juárez Obdulia, García-Sánchez Miguel Ángel, Arellano-Sánchez Ulises, Kornhauser-Straus Isaac, Rojas-González Fernando

机构信息

Department of Chemistry, Universidad Autónoma Metropolitana-Iztapalapa, Av. San Rafael Atlixco 186, Col. Vicentina, México City 09340, Mexico.

出版信息

Materials (Basel). 2016 Nov 4;9(11):898. doi: 10.3390/ma9110898.

Abstract

Special preparation of Santa Barbara Amorphous (SBA)-15, mesoporous silica with highly hexagonal ordered, these materials have been carried out for creating adsorbents exhibiting an enhanced and partially selective adsorption toward CO₂. This creation starts from an adequate conditioning of the silica surface, via a thermo-alkaline treatment to increase the population of silanol species on it. CO₂ adsorption is only reasonably achieved when the SiO₂ surface becomes aminated after put in contact with a solution of an amino alkoxide compound in the right solvent. Unfunctionalized and amine-functionalized substrates were characterized through X-ray diffraction, N₂ sorption, Raman spectroscopy, electron microscopy, Si solid-state Nuclear Magnetic Resonance (NMR), and NH₃ thermal programmed desorption. These analyses proved that the thermo-alkaline procedure desilicates the substrate and eliminates the micropores (without affecting the SBA-15 capillaries), present in the original solid. NMR analysis confirms that the hydroxylated solid anchors more amino functionalizing molecules than the unhydroxylated material. The SBA-15 sample subjected to hydroxylation and amino-functionalization displays a high enthalpy of interaction, a reason why this solid is suitable for a strong deposition of CO₂ but with the possibility of observing a low-pressure hysteresis phenomenon. Contrastingly, CH₄ adsorption on amino-functionalized, hydroxylated SBA-15 substrates becomes almost five times lower than the CO₂ one, thus giving proof of their selectivity toward CO₂. Although the amount of retained CO₂ is not yet similar to or higher than those determined in other investigations, the methodology herein described is still susceptible to optimization.

摘要

已对具有高度六方有序结构的介孔二氧化硅圣巴巴拉无定形(SBA)-15进行了特殊制备,以制备对CO₂具有增强的部分选择性吸附的吸附剂。这种制备从二氧化硅表面的适当预处理开始,通过热碱处理来增加其上硅醇物种的数量。只有当SiO₂表面在与正确溶剂中的氨基醇盐化合物溶液接触后胺化时,才能合理地实现CO₂吸附。通过X射线衍射、N₂吸附、拉曼光谱、电子显微镜、Si固态核磁共振(NMR)和NH₃程序升温脱附对未官能化和胺官能化的底物进行了表征。这些分析证明,热碱处理使底物脱硅并消除了原始固体中存在的微孔(不影响SBA-15毛细管)。NMR分析证实,羟基化固体比未羟基化材料能锚定更多的氨基官能化分子。经过羟基化和氨基官能化的SBA-15样品表现出高的相互作用焓,这就是这种固体适合于CO₂强沉积但可能观察到低压滞后现象的原因。相比之下,CH₄在氨基官能化、羟基化的SBA-15底物上的吸附比CO₂的吸附低近五倍,从而证明了它们对CO₂的选择性。尽管保留的CO₂量尚未与其他研究中确定的量相似或更高,但本文所述的方法仍易于优化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d943/5457248/fb78a5b41838/materials-09-00898-g001.jpg

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