Zbigniew Turzyński

Light scattering characterization of organotin polymers: 1. Tributyltin acrylate copolymer Cutinox-1000

Abstract Laser light scattering including both elastic (integral) and quasielastic measurements, supplemented by intrinsic viscosity data, has been used to characterize a tributyltin acrylate copolymer commercially known as Cutinox-1000 in dilute solution. Four solvents differing in their thermodynamical quality and optical properties were used. Chemical composition heterogeneity of the investigated sample was estimated to be sufficiently small not to influence significantly results of light scattering measurements. Coupled integral and quasielastic light scattering methods were used to determine the molecular weight distribution function, from which the polydispersity of the investigated copolymer sample was estimated to be M¯w/M¯n= 2.1. Determined molecular properties were in reasonable agreement with some theoretical predictions. Conformational parameters, such as the steric factor σ, statistical segment length and R¯H/R¯G ratio, as compared with poly(methyl methacrylate) values suggest some small increase of the copolymer rigidity, probably due to steric hindrance caused by the large metalloorganic side groups.

Characterization by light scattering of simultaneous polymer chain scission and cross-linking processes

Abstract The results of investigations on the changes in molecular parameters, viz. the average molecular weights, M n , M w and M z ; the poly-dispersities M w / M n and M z / M w ; and the translational diffusion coefficient, D 0z , are presented for a polymer sample undergoing simultaneous chain scission and cross-linking. The calculations were carried out within the framework of the model of Saito and Inokuti. The values of D 0z were calculated by the use of the cascade substitution technique. The results of calculations were compared with the experimental results obtained by the light scattering method for polystyrene samples exposed to u.v. radiation with wavelength ⩾ 270 nm in degassed solutions containing CCl4 and CHCl3. Analysis of the results leads to conclusions about the usefulness of the measurement of individual molecular parameters for the detection and characterization of simultaneous chain scission and cross-linking.

Influence of diffusion and induced π-bonds on the ultra-violet radiation-initiated crosslinking of polystyrene in solution

Abstract An attempt has been undertaken to account for the mechanism of polystyrene crosslinking initiated by ultra-violet radiation with wavelengths of λ ⩾ 270 nm in outgassed solutions with CCl 4 and CHCl 3 . The investigations were carried out by the joint method of elastic and quasielastic light scattering, and by the use of absorption spectroscopy in the ultra-violet and visible spectral regions. From the experimental results obtained and the model and theoretical modifications introduced, the crosslinking of polystyrene macromolecules irradiated in solutions with CCl 4 and CHCl 3 is shown to be affected by both the diffusion properties of the macromolecules and the conjugated and isolated double 〉 CC 〈 bonds formed in polymer chains.