Polymer processing radiation dose rate

Polymerizations induced by y radiation proceed by both cationic and free-radical mechanisms. Predominance of the cationic process can be assured by exhaustive purification of monomers and solvents or by employing high radiation dose rates (from electron beam sources). The rate of cationic polymerization has been shown to be strongly influenced by the dielectric constant of the medium, giving rise to discrepancies between radiation-induced bulk polymerizations and chemically initiated solution polymerizations. These discrepancies have been attributed to specific solvation of propagating ions by monomer and polymer. 

Solution polyacrylamides can also be prepared at high polymer soHds by radiation processes (80,81). Polyacrylamides with molecular weights up to 20 million can be prepared by inradiation of acrylamide and comonomers in a polyethylene bag with cobalt-60 gamma radiation at dose rates of 120-200 J/kg-h. The total dose of radiation is controlled to avoid cross-linking. 

Hence, in order to ensure a relatively high rate of radiation-induced polymerization in the emulsion, low dose rates (0.1-1 Gy/s) and low absorbed doses are required. For all these reasons, radiation emulsion polymerization is particularly advantageous from an economical standpoint. Its activation energy, just as for other processes of radical radiation-induced polymerization, is 15-35 kJ/mol. The molecular weight of polymers increases with temperature, as in the case of typical free-radical processes (to a certain extent). This increase is due to an increase in kp with temperature, whereas k, does not depend on the temperature. 

Radiolysis. Radiation degrades both TBP and hydrocarbon diluent in Purex systems, with formation of molecular fragments, polymers, and nitration products. The main product, however, is the same as from hydrolysis, namely, DBP. The yield of DBP in radiolysis of TBP varies somewhat with the diluent used, water content, type of radiation, and dose rate. Baumgartner and Ochsenfeld [B6] cite production of 20 to 30 mg DBP/liter in 30-min exposure of 30 v/o TBP to 0.2 Wh/liter of radiation in mixer-settlers processing fuel cooled 240 days after 33,000 MWd/MT burnup. Because the density of DBP is 1065 g/liter, the volume percent DBP was... 

Sterilisation by high-energy beams, e.g. y rays or fast electrons beams, is very efficient, as these beams are usually not stopped by materials. However, some covalent bonds of the polymeric network can be broken easily by such a high energy. Depending on the type of polymer and the dose and dose rate of the radiation, permanent chain scission or cross-linking can result from this process, modifying the polymeric structure and properties of the material. 

---