Document Type
Dissertation
Degree
Doctor of Philosophy (PhD)
Major/Program
Chemistry
First Advisor's Name
Yong Cai
First Advisor's Committee Title
committee chair
Second Advisor's Name
Barry P. Rosen
Second Advisor's Committee Title
committee member
Third Advisor's Name
Yaroslava Miksovska
Third Advisor's Committee Title
committee member
Fourth Advisor's Name
Anthony McGoron
Fourth Advisor's Committee Title
committee member
Fifth Advisor's Name
Bruce McCord
Fifth Advisor's Committee Title
committee member
Keywords
Raman spectroscopy, : Coffee ring effect, Arsenic speciation
Date of Defense
6-8-2021
Abstract
The coffee ring effect (CRE) phenomenon is originated from the nonuniform solvent evaporation of a sessile droplet deposited onto the flat substrate. Once the evaporation starts, the droplet suspended particles move outwards by the radial flow and concentrate in the edge region of the evaporating droplet, resulting in the formation of the so-called CRE stains. In this work we have expanded the applications of the CRE from separation of particles and macromolecules to small molecules, in particular, coupled to surface-enhanced Raman spectroscopy (SERS). Herein, we have developed a theoretical framework to describe the CRE-driven separation process of small molecules, using SERS analysis of dimethylarsinic acid (DMAV), dimethylmonothioarsinic acid (DMMTAV), and dimethyldithioarsinic acid (DMDTAV) on gold nanofilm (AuNF) as an example. By combining the CRE theory for the radial flow and the Extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory for mass transfer between solution and AuNF surface, we adapted the conventional chromatographic theory to derive a modified van Deemter equation for the CRE-driven separation. By using this model, we predicted the travel distances of arsenicals based on the different affinity of analytes to AuNF and evaluated the possibility of separation of unknown analytes by CRE-based SERS, demonstrating the successful adaptation of classic chromatographic theory to CRE-driven nanochromatography.
Furthermore, we have extrapolated the application of the developed method for the speciation of the peptide-like arsenic-based anticancer drug Darinaparsin (DAR) and its major breakdown product dimethylarsino-cysteine (DMAC). Despite the overlap of DAR and DMAC’s Raman spectra in the final CRE deposit, we were able to identify each compound due to their unique SERS fingerprint. Overall, the developed method was able not only to separate and identify the S-conjugated arsenicals, but at the same time to preserve the DAR and DMAC’s AsIII oxidations state and the fragile As – S moiety, thus providing an alternative speciation method for unstable thioarsenicals. The key advantage of the application of this method for peptides separation is the separation coupled with the mild detection providing the rich structural information of each metabolite.
Identifier
FIDC010228
Previously Published In
Anal. Chem. 2019, 91, 13, 8280–8288
Analytica Chimica Acta, Volume 1106, 15 April 2020, Pages 88-95
Recommended Citation
Liamtsau, Valery, "In Situ Arsenic Speciation using Surface-enhanced Raman Spectroscopy and the Coffee Ring Effect" (2021). FIU Electronic Theses and Dissertations. 4711.
https://digitalcommons.fiu.edu/etd/4711
Included in
Environmental Health Commons, Other Pharmacology, Toxicology and Environmental Health Commons, Toxicology Commons
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