UWSpace is currently experiencing technical difficulties resulting from its recent migration to a new version of its software. These technical issues are not affecting the submission and browse features of the site. UWaterloo community members may continue submitting items to UWSpace. We apologize for the inconvenience, and are actively working to resolve these technical issues.
 

¹H MAS NMR Spectral Coalescence of Water and Hydroxyl Resonances in MCM-41

dc.comment.hiddenThank-you for reviewing my thesis :)en
dc.contributor.authorWalia, Jaspreet
dc.date.accessioned2011-09-01T18:59:13Z
dc.date.available2011-09-01T18:59:13Z
dc.date.issued2011-09-01T18:59:13Z
dc.date.submitted2011
dc.description.abstractSolid state ¹H MAS NMR spectroscopy was used to investigate the temperature and hydration dependance of water and hydroxyl proton spectra of hydrated mesoporous MCM-41. The NMR spectra show a complex peak structure, with hydroxyl proton resonances seen in dry MCM-41 disappearing as water is introduced into the pores, and new peaks appearing representing water and hydrated silanol groups. Until now the assignment of these peaks was unclear and the consensus was that magnetization exchange played an important role in the coalescence of the various peaks which appear in the spectra. It was found recently that magnetization exchange is not necessary to produce the spectral featured observed [Niknam, M., M.Sc. Thesis, University of Waterloo (2010)]. In the present study a simplified model, based on chemical shift averaging by the making and breaking of hydrogen bonds as water undergoes rotational motion and translational self-diffusion on the pore surface, has been developed to explain the NMR spectral results. The model is able to reproduce the experimental ¹H MAS NMR spectra for all hydrations and temperatures studied. For the first time, definitive spectral assignments for all hydroxyl and water protons in the sample has been achieved. Spectral features arising due to temperature change have been explained by using the known result that the proton chemical shift of a hydrogen atom involved in hydrogen bonding varies linearly with temperature. Furthermore, it is reported for the first time, that with increasing hydration, water molecules begin to favour forming two hydrogen bonds to the surface. This may represent the first step in the pore filling process.en
dc.identifier.urihttp://hdl.handle.net/10012/6234
dc.language.isoenen
dc.pendingfalseen
dc.publisherUniversity of Waterlooen
dc.subjectMCM-41en
dc.subjectCoalescenceen
dc.subjectNMRen
dc.subjectWateren
dc.subject.programPhysicsen
dc.title¹H MAS NMR Spectral Coalescence of Water and Hydroxyl Resonances in MCM-41en
dc.typeMaster Thesisen
uws-etd.degreeMaster of Scienceen
uws-etd.degree.departmentPhysics and Astronomyen
uws.peerReviewStatusUnrevieweden
uws.scholarLevelGraduateen
uws.typeOfResourceTexten

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Walia_Jaspreet.pdf
Size:
5.69 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
250 B
Format:
Item-specific license agreed upon to submission
Description: