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Solid-state 13C, 15N and 29Si NMR characterization of block copolymers with CO2 capture properties
Luleå University of Technology, Department of Civil, Environmental and Natural Resources Engineering, Chemical Engineering.ORCID iD: 0000-0003-3652-7798
Luleå University of Technology, Department of Engineering Sciences and Mathematics, Material Science.ORCID iD: 0000-0003-4888-6237
Department of Chemistry, Quaid-i-Azam University, Islamabad.
Department of Chemistry, Quaid-i-Azam University, Islamabad.
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Number of Authors: 52016 (English)In: Magnetic Resonance in Chemistry, ISSN 0749-1581, E-ISSN 1097-458X, Vol. 54, no 9, p. 734-739Article in journal (Refereed) Published
Abstract [en]

Natural abundance solid-state multinuclear (13C, 15N and 29Si) cross-polarization magic-angle-spinning NMR was used to study structures of three block copolymers based on polyamide and dimethylsiloxane and two polyamides, one of which including ferrocene in its structure. Assignment of most of the resonance lines in 13C, 15N and 29Si cross-polarization magic angle-spinning NMR spectra were suggested. A comparative analysis of 13C isotropic chemical shifts of polyamides with and without ferrocene has revealed a systematic shift towards higher δ -values (de-shielding) explained as the incorporation of paramagnetic ferrocene into the polyamide backbone. In addition, the 13C NMR resonance lines for ferrocene-based polyamide were significantly broadened, because of paramagnetic effects from ferrocene incorporated in the structure of this polyamide polymer. Single resonance lines with chemical shifts ranging from 88.1 to 91.5ppm were observed for 15N sites in all of studied polyamide samples. 29Si chemical shifts were found to be around 22.4ppm in polydimethylsiloxane samples that falls in the range of chemical shifts for alkylsiloxane compounds. The CO2 capture performance of polyamide-dimethylsiloxane-based block copolymers was measured as a function of temperature and pressure. The data revealed that these polymeric materials have potential to uptake CO2 (up to 9.6 cm3 g1) at ambient pressures and in the temperature interval 30–40 °C. Copyright ©2016 John Wiley & Sons, Ltd.

Place, publisher, year, edition, pages
2016. Vol. 54, no 9, p. 734-739
National Category
Physical Chemistry Other Materials Engineering
Research subject
Chemistry of Interfaces; Engineering Materials
Identifiers
URN: urn:nbn:se:ltu:diva-13154DOI: 10.1002/mrc.4440ISI: 000382969800006PubMedID: 27133214Scopus ID: 2-s2.0-85021984706Local ID: c55b7ed5-d822-4d84-8d45-7ff80837aab5OAI: oai:DiVA.org:ltu-13154DiVA, id: diva2:986106
Note

Validerad; 2016; Nivå 2; 20160502 (faisha)

Available from: 2016-09-29 Created: 2016-09-29 Last updated: 2018-12-14Bibliographically approved

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Shah, Faiz UllahAkhtar, FaridAntzutkin, Oleg

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