Abstract The nonaqueous solution behavior of random copolymers of styrene (ST) with sodium‐2‐acrylamido‐2‐methylpropane sulfonate (Na‐AMPS) [poly(ST‐Na‐AMPS)] has been investigated using the transient electric birefringence (TEB) technique. The copolymers with varying high sulfonate contents (about 30–70 mol%), bridging the gap between conventional ionomers and classical polyelectrolytes, were dissolved in the solvent methylformamide (MFA) with a high permittivity ϵ of ca. 190. The solutions showed a negative birefringence at electric field strength E of the order of kV/cm. A typical Kerr effect was observed at low polymer concentrations C of ca. 10 −3 g/mL and electric field strengths of the order of kV/cm. However, the detailed, TEB studies demonstrated different behavior at two concentration regimes in dilute solution. At a low concentration regime (e.g., C ≤ 1 × 10 −3 g/mL for the copolymer with a 66.7 mol % sulfonate content) where the reduced viscosity exhibited a pronounced polyelectrolyte effect, the birefringence signal pattern showed a maximum before reaching a steady value. Additionally, during the rise at an applied electric field strength beyond a threshold value, it was observed that the nonexponential field‐free decay was slower than the single exponential field‐induced rise. The observed anomalous behavior was similar to those of a polyelectrolyte [sodium poly (styrene sulfonate)] in aqueous solution and might be attributed to the perturbation of the molecular shape by the applied electric field. At the higher concentration regime (e.g., C ≥ 4 × 10 −3 g/mL for the same copolymer with a 66.7 mol % sulfonate content) where the polyelectrolyte effects started to diminish as indicated by the viscosity study, the birefringence shape showed no variation with an increased electric field strength and the field‐free decay turned out to be faster than the single exponential rise. The dissociation of ionic aggregates was tentatively interpreted to be responsible for this observation. It seems that by simply varying the polymer concentration, poly (ST‐Na‐AMPS) could behave either as a polyelectrolyte or as an ionomer in a single polar organic solvent.
A new and simple method has been reported here which can be applied to control simultaneously the shape and size of the copper nanoparticles, without using any ca p ping agent or template. By this method, cube -shaped copper nanoparticles in the size range ~ 75 –250 nm were formed from smaller spherical co p-per particles. At the first stage, 5–6 nm spherical co p per particles were prepared from aqueous copper sulphate solution by borohydride reduction. In the second stage, these small particles were mixed with ap propriate amount of copper sulphate and sodium ascorbate, which resulted in the production of larger size cu bic copper particles. In the latter step, the new grown larger particles acted as seed and grew larger due to the reduction of copper ions by ascorbate ion on their surfaces. Thus cubic copper nanoparticles of varied size regime were produced by ascorbate ion by var ying the ratio of copper seed particles to copper ion concentrations in solution. M