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Post-Synthesis Functionalization of Porous Organic Polymers for CO2 Capture

机译:多孔有机聚合物的合成后功能化以捕集二氧化碳

摘要

Solid porous materials are network materials that contain space void. Porous Organic Polymers (POPs) are porous materials, which are constructed from organic building blocks and exhibit large surface area with low densities. Due to these characteristics, POPs have attracted attentions because of their potential use in application such as gas storage and chemical separation.This thesis presents a study of the synthesis of novel POP being a network based on 2,5- dibromobenzaldehyde and 1,3,5-triethynylbenzene linked together via Sonogashira- Hagihara (SH) coupling. This network showed a relatively good surface area of 770 m2/g and total pore volume of 0.59 cc/g. In addition, it proved to be chemically and thermally stable, maintaining the thermal stability up to 350oC.In addition to synthesize novel aldehyde-POP network, it was also possible to post synthetically modify a network via one-step post synthetic functionalization by amine. Ethelynediamine (EDA), Diethylenetriamine (DETA), and Tris(2-aminoethyl)amine (Tris-amine) are three different amines used for aldehyde-POP functionalization. The produced networks were aminated via different amine species substitution the aldehyde group present within the network. Modification to these networks resulted in a decrease in surface area from 770 m2.g-1 to 333 m2.g-1, 162 m2.g-1, and 211 m2.g-1 in respective to EDA, DETA, and Tris-amine. Although the surface areas were decreased, the CO2 adsorption was enhanced as evidenced by the increase of Qst (i.e., from 25 to 45 kJ.mol-1 for DETA at low coverage).Our findings are expected to strengthen existing research areas of the influence of different type of amines (e.g aromatic amine) on CO2 adsorption. Although amine grafting has been studied in other systems (e.g., PAFs and MOFs), we are the first to reported amine functionalized POPs using a novel one-step amine grafting PSM procedure. Future research might extend to study the interaction between CO2 and amine species under real working conditions.
机译:固体多孔材料是包含空间空隙的网络材料。多孔有机聚合物(POPs)是多孔材料,由有机结构单元构造而成,并具有较大的表面积和低密度。由于这些特性,POPs因其在储气和化学分离等应用中的潜在用途而备受关注。本文提出了一种新型的以2,5-二溴苯甲醛和1,3为基础的网络合成POPs的研究。 5-三乙炔基苯通过Sonogashira-Hagihara(SH)偶联连接在一起。该网络显示相对较好的表面积为770 m2 / g,总孔体积为0.59 cc / g。此外,它被证明是化学和热稳定的,可保持高达350oC的热稳定性。除了合成新型的醛-POP网络外,还可以通过胺的一步合成后官能化来合成后修饰网络。乙二胺(EDA),二亚乙基三胺(DETA)和三(2-氨基乙基)胺(Tris-amine)是用于醛POP官能化的三种不同的胺。产生的网络通过不同的胺种类取代网络中存在的醛基而被胺化。对这些网络的修改导致EDA,DETA和Tris-e的表面积分别从770 m2.g-1减少到333 m2.g-1、162 m2.g-1和211 m2.g-1。胺。尽管表面积减少了,但Qst的增加证明了CO2吸附的增加(即低覆盖DETA从25 kJ.mol-1增加到45 kJ.mol-1)。我们的发现有望加强现有研究的影响不同类型的胺(例如芳族胺)对CO2吸附的影响。尽管已经在其他系统(例如PAF和MOF)中研究了胺接枝,但我们是第一个使用新型一步式胺接枝PSM方法报道胺官能化的POPs的公司。未来的研究可能会扩展到研究实际工作条件下CO2与胺类之间的相互作用。

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    Al Otaibi Mona S.;

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  • 年度 2014
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