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A new spectrophotometric method for determination of residual polydiallyldimethylammonium chloride flocculant in treated water based on a diazotization-coupled ion pair
Author(s) -
IW Mwangi,
J. Catherine Ngila,
Patrick Ndungu
Publication year - 2012
Publication title -
water sa
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.389
H-Index - 59
eISSN - 1816-7950
pISSN - 0378-4738
DOI - 10.4314/wsa.v38i5.8
Subject(s) - chemistry , potentiometric titration , chloride , spectrophotometry , nuclear chemistry , inorganic chemistry , chromatography , ion , organic chemistry
Polydiallyldimethylammonium chloride (polyDADMAC) is a water-soluble cationic polyelectrolyte used for water treatment. Its residues in treated water are contaminants as they react with chlorine to produce a carcinogenic compound. Commonly-used techniques for quantification of the polycation, such as colloidal and potentiometric titration as well as 1 H NMR, have poor sensitivity and detection limits. This paper describes a more sensitive UV spectrophotometric method for quantitative determination of residual polyDADMAC in treated water, through formation of an ion pair with (4-hydroxy1-napthylazo) benzene-sulphonic acid (dye). The ion pair, which is a colloidal solid material, was characterised by FTIR, 13 C NMR and 1 H NMR techniques. The colloid materials formed with different concentrations of polyDADMAC were dissolved in either N,N-dimethylformamide or 1,4-dioxane, followed by determination with UV spectrophotometry. The wavelength of maximum absorption (λ max ) was found to be dependent on the solvent used, with 1,4-dioxane showing a better linear range of 0.1–1.8 mg∙l -1 polyDADMAC. Varying the pH of the solutions had no significant effect on λmax.

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