Conductometric titration, latexes serum replacement

Conductometric titration of the surface groups gave a surface charge density of strong acid (-S0 ) of 0.56 C/g and of weak acid (-COO ) of 0.23 C/g. Preceding the conductometric titration the latex was cleaned by serum replacement with doubly distilled water and 5 10 M HCl as described in ref. ( 3). 

Polystyrene latexes have been prepared using persulfate initiator for many years, but only recently have methods been developed to determine the number and loci of the sulfate surface groups. To determine these surface groups, the latex is cleaned to remove the adsorbed emulsifier and solute electrolyte, then the surface sulfate groups in the H+ form are titrated conductometrically with base. The latexes can be cleaned effectively by ion exchange (2-5) or serum replacement (6) dialysis is not effective in removing the adsorbed emulsifier and solute electrolyte (3,5,6). +... 

For serum replacement (6), the latex is confined in a cell with a uniform-pore-size Nuclepore filtration membrane. Distilled, deionized water is pumped through the latex until the conductance of the effluent stream is about the same as that of the distilled, deionized water. This serum replacement removes the adsorbed emulsifier and solute electrolyte quantitatively and allows recovery of the serum in a form suitable for further analysis however, it does not+replace the Na+ and K counterions of the surface groups with Vl ions. To do this, dilute hydrochloric acid (ca. 10 N) is pumped through the latex, followed by distilled, deionized water to remove the excess acid. The latex is then titrated conductometrically to determine the surface charge. 

The latex was cleaned by ion exchange and serum replacement, which gave the cleaned latex plus six serum fractions. The cleaned latex and the serum samples were analyzed by conductometric titration. Also, the amount of anionic emulsifier in the serum was determined by Fyamine 1622 colorimetric titration and thin-film chromatography, and the amount of nonionic emulsifier by iodine-iodide colorimetric titration and thin-film chromatography. 

A polyvinyl acetate latex prepared by semi-continuous polymerization at 55° using a polymethacrylic acid-nonylphenol-poly-ethoxylate phosphate ester emulsifier and sodium persulfate-sodium formaldehyde sulfoxylate initiator (23). The latex was cleaned by ion exchange and serum replacement using both Nuclepore and Pellicon membranes, and the cleaned latex and serum fractions were analyzed by conductometric titration. In addition, the dried films were extracted with water and organic solvents, and the extracts were analyzed by infrared spectroscopy and thermo-gravimetric analysis. 

The latexes were cleaned by ion exchange and serum replacement, and the number and type of surface groups were determined by conductometric titration. The molecular weight distributions of the polymers were determined by gel permeation chromatography. The stability of the latexes to added electrolyte was determined by spectrophotometry. The compositional distribution was determined by dynamic mechanical spectroscopy (Rheovibron) and differential scanning calorimetry, and the sequence distribution by C13 nuclear magnetic resonance. 

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