Differential scanning calorimetry and thermogravimetry studies of polyacrylamide prepared by free-radical polymerization in inverse microemulsion and in solution
✍ Scribed by Ivica Janigová; Katarína Csomorová; Martina Stillhammerová; Jaroslav Bartoň
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 320 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
In spite of the free‐radical polymerization of acrylamide in different reaction environments (non‐percolating (A) and/or percolating (B) inverse microemulsions, water/isopropanol solution (C)) the polyacrylamides obtained did not differ in their T~g~ values (A: 468 K; B: 469 K; C: 468 K). Similarly, the course of thermogravimetry curves for all three samples A, B and C, was practically identical. The results confirmed that the spatially oriented array of acrylamide molecules at the water/oil interface of the inverse micellar system was destroyed already at early stages of polymerization. The formation of longer polymer chains due to the polymerization at water/oil interface was thus restricted or even eliminated in favor of the propagation of polyacrylamide growing chains in isotropic conditions of water pools of inverse micelles.
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## Abstract The molecular characteristics of poly(__N__‐isopropylacrylamide) (PNIPA), prepared by free‐radical polymerization using an aqueous redox initiator and reaction conditions comparable to those used in the synthesis of nanocomposite gels, were investigated by altering the monomer concentra