Browsing by Author "Li, Lingling"
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Item Rheological Properties and Reaction Kinetics of Amidoamine Oxide Surfactants-based Acids with Calcite(2012-07-16) Li, LinglingA new type of viscoelastic amphoteric surfactants (amidoamine oxide) has been examined as a diverting agent during acidizing treatment. Rheological properties of viscoelastic surfactants are a function of surfactant concentration, acid additives, pH, temperature and shear rate. A HPHT rheometer was used to test the effect of common acid additives and organic acids/chelating agents on the apparent viscosity of amidoamine oxide-based acids. The compatibility and thermal stability of surfactants with corrosion inhibitor were also investigated. Rotating disk apparatus was used to examine the kinetic studies of surfactant-based acids with limestone. The results show that the apparent viscosity of surfactant solutions prepared in deionized water, live acid, and spent acid was found to be a function of temperature. Apparent viscosity of live surfactant-based acids was also found to be a function of HCl concentration. Most of acid additives could adversely affect the rheological properties of spent acids. Compatibility tests should be done prior the field application. Cryo-TEM studies show the changes of rod-like micelle structures with the addition of additives. The reaction between surfactant-based acid and limestone was found to be mass transfer limited at 170 degrees F.Item Water-soluble bodipys: syntheses, derivatization and photophysical studies(2009-05-15) Li, LinglingA set of water-soluble 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) derivatives, has been prepared and their spectroscopic properties examined. These dyes can be used as either donor or acceptor in synthesis of through-bond energy transfer cassettes. Sulfonation conditions were developed for several BODIPY dyes to give the mono-sulfonated and di-sulfonated products. Compounds with an aryl iodide could be used for organometallic couplings. Similarly, BODIPYs with an aromatic bromide, but also two chlorine atoms could be replaced via SNAr reactions. The amine sulfonated BODIPY is amenable to couple to biomolecules via acylation reactions. A diazotization/azide reaction sequence was used to convert the amines into azides; the latter may be functionalized via click reactions. Spectral data for these materials indicates they are highly fluorescent probes in aqueous environments. We have also prepared some lipophilic BODIPY derivatives, which can be used for SNAr reactions and make some through-bond, energy transfer cassettes. DichloroBODIPYs can also be used for labeling proteins successfully.