## Abstract **Summary:** Solution properties of alternating polyampholytes based on __N__,__N__‐dimethyldiallylammonium chloride and maleic acid as well as __N__,__N__‐dimethyldiallylammonium and maleamic acid (butylmaleamic acid, phenylmaleamic acid, 4‐butylphenylmaleamic acid) were studied in aqu
Potentiometric Behavior of Polyampholytes Based on N,N′-diallyl-N,N′-dimethylammonium Chloride and Maleamic Acid Derivatives
✍ Scribed by Mabya Fechner; Joachim Koetz
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 765 KB
- Volume
- 212
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Strongly alternating copolymers (PalH, PalPh, PalPhBisCarb) composed of N,N′‐diallyl‐N,N′‐dimethyl‐ammonium chloride (DADMAC) and maleamic acid derivatives (MAD) are synthesized by a water‐based free radical copolymerization using 4,4‐azobis(4‐cyanovaleric acid) (V501) as the initiator. The structure of the copolymers is verified by ^1^H‐NMR, elemental analysis, and thermogravimetric measurements, and the physicochemical properties are investigated by viscometric and potentiometric techniques. Potentiometric titration curves show that the acidity of the carboxylic groups strongly depends on the degree of dissociation and the ionic strength. Since all copolymers behave as polycations at low degree of dissociation, a transition from an extended chain to a coil conformation can be identified by reaching the isoelectric point (IEP).
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The retention behavior of N-trifluoroacetyl-0-alkyl esters of selected amino acids with various types of alkyls in ester group was studied by capillary gas chromatography with modified cyclodextrin stationary phases. A model set of six different esters of five amino acids was analyzed on two columns