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Hydrolysis of Poly(acrylamide) ‐ Starch Graft Copolymer
Author(s) -
Khalil M. I.,
Farag S.,
Fattah S. Abd El
Publication year - 1996
Publication title -
starch ‐ stärke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.62
H-Index - 82
eISSN - 1521-379X
pISSN - 0038-9056
DOI - 10.1002/star.19960480708
Subject(s) - sodium hydroxide , copolymer , hydrolysis , starch , chemistry , hydrochloric acid , amide , acrylamide , polymer chemistry , hydroxide , phosphoric acid , sodium , acid hydrolysis , nuclear chemistry , inorganic chemistry , organic chemistry , polymer
Poly(acrylamide)‐starch graft copolymer was treated independently with sodium hydroxide and different acid solutions. The different acids include phosphoric, hydrochloric and sulphuric acid. The treatment was carried out under a variety of conditions including sodium hydroxide concentration, time and duration of hydrolysis as well as type of acid used. The extent of hydrolysis was assessed by estimating amide and carboxyl content as well as the acrylate and starch content before and after treatment. It was found that the increment in carboxyl content is equal to the decrement in amide on using sodium hydroxide concentration up to 1n , while using higher concentrations than 1n lead to differences in formed carboxyl and decreased amide groups. The magnitude of this difference depends on sodium hydroxide concentration as well as temperature and duration of hydrolysis. The maximum value of carboxyl content obtained was 593 m‐eq/100g sample. The acidic treatment of the starch copolymer does not affect the conversion of amide groups to carboxyl groups and the lonely effect was hydrolysis of starch component of the copolymer. Evaluation of the alkali teated copolymer as cation exchanger was carried out. The absorption efficiency % of different cations depends on the associated anions and follow the order: Cu 2+ > Zn 2+ > Co 2+ Mg 2+ .