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    Post-Synthesis Functionalization of Porous Organic Polymers for CO2 Capture

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    Thesis
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    Type
    Thesis
    Authors
    Al Otaibi, Mona S.
    Advisors
    Eddaoudi, Mohamed cc
    Committee members
    Takanabe, Kazuhiro cc
    Han, Yu cc
    Program
    Chemical Science
    KAUST Department
    Physical Science and Engineering (PSE) Division
    Date
    2014-07
    Embargo End Date
    2015-07-20
    Permanent link to this record
    http://hdl.handle.net/10754/324902
    
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    Access Restrictions
    At the time of archiving, the student author of this thesis opted to temporarily restrict access to it. The full text of this thesis became available to the public after the expiration of the embargo on 2015-07-20.
    Abstract
    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.
    Citation
    Al Otaibi, M. S. (2014). Post-Synthesis Functionalization of Porous Organic Polymers for CO2 Capture. KAUST Research Repository. https://doi.org/10.25781/KAUST-WXFPB
    DOI
    10.25781/KAUST-WXFPB
    ae974a485f413a2113503eed53cd6c53
    10.25781/KAUST-WXFPB
    Scopus Count
    Collections
    MS Theses; Physical Science and Engineering (PSE) Division; Chemical Science Program

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