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Guor-Tzo Wei

Publications and source records attributed to Guor-Tzo Wei.

4 recordsLinked to original sources
PubMed2006

Extraction of nanosize copper pollutants with an ionic liquid.

Speciation and possible reaction paths of nanosize copper pollutants extracted with a RTIL (room-temperature ionic liquid ([C4mim][PF6], 1-butyl-3-methylimidazolium hexafluorophosphate)) have been studied in the present work. Experimentally, in a very short contact time (2 min), 80-95% of nanosize CuO as well as other forms of copper (such as nanosize Cu, Cu2+, or Cu(II)(ads) (in the channels of MCM-41)) in the samples could be extracted into the RTIL. The main copper species extracted in the RTIL as observed by XANES (X-ray absorption near edge structure) were Cu(II). Existence of Cu-N bondings with coordination numbers (CNs) of 3-4 for copper extracted in the RTIL was found by EXAFS (extended X-ray absorption fine structural) spectroscopy. Interestingly, chelation of Cu(II) with 1-methylimidazole (MIm) in the RTIL during extraction was also observed by 1H NMR (nuclear magnetic resonance). At least two possible reaction paths for the rapid extraction of nanosize copper pollutants with the RTIL might occur: (1) an enhanced dissolution of nanosize CuO (to form Cu2+) and (2) formation of [Cu(MIm)4(H2O)2]2+ that acted as a carrier of copper into the RTIL matrix.

Copper↗
PubMed2004

Aqueous-organic phase transfer of gold nanoparticles and gold nanorods using an ionic liquid.

The water-immiscible ionic liquid, [C4MIM][PF6], is a solvent medium that allows complete transfer of gold nanoparticles from an aqueous phase into an organic phase. Both spherical and rod-shaped gold nanoparticles are efficiently transferred from an aqueous solution into the organic phase without requiring the use of thiols. The sizes and shapes of the gold nanoparticles were preserved during the phase-transfer process when a surfactant was added to the ionic liquid. This process offers a simple approach for obtaining solutions of differently sized and shaped gold nanoparticles in ionic liquids.

Journal Article↗
PubMed2002

Electroosmotic flow controllable coating on a capillary surface by a sol-gel process for capillary electrophoresis.

A simple coating procedure employing a sol-gel process to modify the inner surface of a bare fused-silica capillary with a positively charged quaternary ammonium group is established. Scanning electron microscopic studies reveal that a smooth coating with 1 to approximately 2 microm thickness can be obtained at optimized coating conditions. With 40 mM citrate as a running electrolyte, the plot of electroosmotic flow (EOF) versus pH shows a unique three-stage EOF pattern from negative to zero and then to positive over a pH range of 2.5 to 7.0. At pH above 5.5, the direction of the EOF is from the anode to the cathode, as is the case in a bare fused-silica capillary, and the electroosmotic mobility increases as the pH increases. However, the direction of the EOF is reversed at pH below 4.0. Over the pH range of 4.0 to 5.5, zero electroosmotic mobility is obtained. Such a three-stage EOF pattern has been used to separate six aromatic acids under suppressed EOF and to separate nitrate and nitrite with the anions migrating in the same direction as the EOF. The positively charged quaternary ammonium group on the coating was also utilized to minimize the adsorption problem during the separation of five basic drugs under suppressed EOF and during the separation of four basic proteins with the cations migrate in the opposite direction as the EOF. Also, the stability and reproducibility of this column are good.

Electrophoresis, Capillary↗