Dynamic surface tension analysis of dodecyl sulfate association complexes. 2001

W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
Department of Chemistry, Box 351700, Center for Process Analytical Chemistry, University of Washington, Seattle WA 98195-1700, USA.

First, a novel calibration method is used to expand the current understanding of spherical drop growth and elongation that occurs during on-line measurements of surface pressure using the dynamic surface tension detector (DSTD). Using a novel surface tension calibration method, the drop radius is calculated as a function of time from experimental drop pressure data and compared to the theoretical drop radius calculated from volumetric flow rate. From this comparison, the drop volume at which the drop shape starts to deviate ( approximately 4 mul) from a spherical shape is readily observed and deviates more significantly by approximately 6 mul drop volume (5% deviation in the ideal spherical drop radius) for the capillary sensing tip employed in the DSTD. From this assessment of drop shape, an experimental method for precise drop detachment referred to as pneumatic drop detachment is employed at a drop volume of 2 mul (two second drops at 60 mul/min) in order to provide rapid dynamic surface tension measurements via the novel on-line calibration methodology. Second, the DSTD is used to observe and study kinetic information for surface-active molecules and association complexes adsorbing to an air-liquid drop interface. Dynamic surface tension measurements are made for sodium dodecyl sulfate (SDS) in the absence and presence of either tetra butyl ammonium (TBA) or chromium (III). Sensitive, indirect detection of chromium and other multiply charged metals at low concentrations is also investigated. The DSTD is utilized in examining the dynamic nature of SDS: cation association at the air-liquid interface of a growing drop. Either TBA or Cr(III) were found to substantially enhance the surface tension lowering of dodecyl sulfate (DS), but the surface tension lowering is accompanied by a considerable kinetic dependence. Essentially, the surface tension lowering of these DS: cation complexes is found to be a fairly slow process in the context of the two second DSTD measurement. The limit of detection for both SDS and chromium (III) is in the 300-400 part-per-billion (by mass) range.

UI MeSH Term Description Entries

Related Publications

W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
January 2010, Langmuir : the ACS journal of surfaces and colloids,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
June 2022, Langmuir : the ACS journal of surfaces and colloids,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
November 2010, The journal of physical chemistry. B,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
June 2002, Journal of colloid and interface science,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
October 1979, Biochemistry,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
October 1975, Analytical biochemistry,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
March 2019, Journal of colloid and interface science,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
October 1970, The Journal of biological chemistry,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
March 1983, Biochimica et biophysica acta,
W W Quigley, and A Nabi, and B J Prazen, and N Lenghor, and K Grudpan, and R E Synovec
June 1976, Biochemistry,
Copied contents to your clipboard!