| In this paper, acrylamide homopolymer and copolymer with star structure were synthesized. The single electron transfer living radical polymerization menthod(SET-LRP) was used to synthesis binary copolymer by using acrylamide(AM), sodium acrylate(AA-Na) and 2-acrylamide-2-methylpropane sulfonate(NaAMPS) as the monomers.The influence to reaction investigated at different conditions were as follows.1ã€Tris(2-aminoethyl)amine(Me6-TREN) was synthesized by using TREN, formaldehyde and methanoic acid as the monomers at 120±0.1 ℃.And the products were characterized via FT-IR and 1H NMR. The results showed that the products which synthesized were target products.2ã€Using acrylamide(AM) as monomer, using Cu as catalyst, using hexamethy-tris(2-aminoethyl) amine(Me6-TREN) as ligand, using chloroform and terachloroethane as initiator respectively, and water as solvent, the SET-LRP method was used to synthesis polyacrylamide at 25.0±0.1 ℃. And the products were characterized via FT-IR. The result showed that the products which synthesized were target products.3ã€Using chloroform as initiator,using acrylamide(AM) as monomer,using Cu as catalyst, using hexamethy-tris(2-aminoethyl) amine(Me6-TREN) as ligand, and water as solvent, the SET-LRP method was used to synthesis binary copolymer P(AM-co-AA-Na)and P(AM-co-AMPS)at 25.0±0.1 ℃. And the products were characterized via FT-IR. The result showed that the products which synthesized were target products.4ã€The effect to binary copolymerization was investigated via CuCl2, catalyst, initiator and temperature. The results showed that with the time increasing, the conversion rate incrased linearly. ln([M]0/[M])and time also showed good linear relationship which performed first-order kinetics. This indicated that the polymerization was a living polymerization.With the temperature increasing, monomer conversion rising, ln([M]0/[M])and time also showed good linear relationship, the relative molecular mass of the polymer showed a trend of first increases and then.With the amount of catalyst increasing, monomer conversion, ln([M]0/[M])and the relative molecular mass of the polymer showed a trend of first increases and then. With the amount of initiator increasing, monomer conversion rised, ln([M]0/[M]) decreased and monomer conversion reduced. |