Preparation and Characterization of Colloidal Silica Particles under Mild Conditions

2012 ◽  
Vol 89 (7) ◽  
pp. 940-942 ◽  
Author(s):  
Frances Neville ◽  
Azrinawati Mohd. Zin ◽  
Graeme J. Jameson ◽  
Erica J. Wanless
Langmuir ◽  
1996 ◽  
Vol 12 (15) ◽  
pp. 3709-3715 ◽  
Author(s):  
I. Dékány ◽  
L. Nagy ◽  
L. Túri ◽  
Z. Király ◽  
N. A. Kotov ◽  
...  

1999 ◽  
Vol 566 ◽  
Author(s):  
Jin-Goo Park ◽  
Sang-Ho Lee ◽  
Hyoung-Gyun Kim

The purpose of this study was to explore the interaction between slurry particles and wafer surfaces by the measurements of their zeta potentials. The zeta potentials of slurry particles such as fumed and colloidal silica, alumina, ceria and MnO2 and substrates such as silicon, TEOS, W, and Al have been measured by electrophoretic and electroosmosis method to evaluate the electrical properties of surfaces, respectively. The zeta potential of oxide and metal surfaces showed similar values to those of particles as a function of pH. The interaction energy between alumina and silica particles and TEOS, W and Al substrate were calculated based on DLVO theory. No deposition of silica particles on TEOS and the heavy deposition of alumina particles on metal substrates were observed in the particle deposition test. Experimental results were well agreed with the theoretical calculation.


Langmuir ◽  
1996 ◽  
Vol 12 (10) ◽  
pp. 2608-2610 ◽  
Author(s):  
Toshiki Konishi ◽  
Eiji Yamahara ◽  
Norio Ise

2020 ◽  
Author(s):  
Joel D. Smith ◽  
George Durrant ◽  
Daniel Ess ◽  
Warren Piers

<div>The synthesis and characterization of an iridium polyhydride complex (Ir-H4)</div><div>supported by an electron-rich PCP framework is described. This complex readily loses molecular</div><div>hydrogen allowing for rapid room temperature hydrogen isotope exchange (HIE) at the hydridic</div><div>positions and the α-C-H site of the ligand with deuterated solvents such as benzene-d6, toluene-d8</div><div>and THF-d8. The removal of 1-2 equivalents of molecular H2 forms unsaturated iridium carbene</div><div>trihydride (Ir-H3) or monohydride (Ir-H) compounds that are able to create further unsaturation</div><div>by reversibly transferring a hydride to the ligand carbene carbon. These species are highly active</div><div>hydrogen isotope exchange (HIE) catalysts using C6D6 or D2O as deuterium sources for the</div><div>deuteration of a variety of substrates. By modifying conditions to influence the Ir-Hn speciation,</div><div>deuteration levels can range from near exhaustive to selective only for sterically accessible sites.</div><div>Preparative level deuterations of select substrates were performed allowing for procurement of</div><div>>95% deuterated compounds in excellent isolated yields; the catalyst can be regenerated by</div><div>treatment of residues with H2 and is still active for further reactions.</div>


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