1985
DOI: 10.1088/0305-4470/18/15/026
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The kinetics of cluster fragmentation and depolymerisation

Abstract: The equation that describes fragmentation kinetics, such as that which occurs in cluster breakup and polymer chain degradation (depolymerisation), is solved for models where the rate of breakup depends upon the size of the object breaking up. The resulting dynamic scaling behaviour is investigated. Both discrete and continuous models are considered.

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Cited by 359 publications
(298 citation statements)
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“…additional influences also play a role), and particle shape can be accounted for by averaging overall possible particle shape [69]. The models used to describe these degradation process are often frequently complicated, but as a general rule focus on chain scission in the polymer backbone through (a) random chain scission (all bonds break with equal probability) characterised by oxidative reactions; (b) scission at the chain midpoint dominated by mechanical degradation; (c) chain-end scission, a monomer-yielding depolymerisation reaction found in thermal and photodecomposition processes; and (d) in terms of inhomogeneity (different bonds have different breaking probability and dispersed throughout the system) [71][72][73]. The estimation of degradation half-lives has also been considered for strongly hydrolysable polymers through the use of exponential decay eqs.…”
Section: Environmental Persistence and Degradationmentioning
confidence: 99%
“…additional influences also play a role), and particle shape can be accounted for by averaging overall possible particle shape [69]. The models used to describe these degradation process are often frequently complicated, but as a general rule focus on chain scission in the polymer backbone through (a) random chain scission (all bonds break with equal probability) characterised by oxidative reactions; (b) scission at the chain midpoint dominated by mechanical degradation; (c) chain-end scission, a monomer-yielding depolymerisation reaction found in thermal and photodecomposition processes; and (d) in terms of inhomogeneity (different bonds have different breaking probability and dispersed throughout the system) [71][72][73]. The estimation of degradation half-lives has also been considered for strongly hydrolysable polymers through the use of exponential decay eqs.…”
Section: Environmental Persistence and Degradationmentioning
confidence: 99%
“…Such equations play an important role in reversible polymerization processes and in related aggregation and fragmentation processes. [30][31][32][33][34][35] In our model, the variable window sizes for the chain fusion/fragmentation processes and for the irreversible mechanical breakage of chains imposes somewhat intricate constraints on the corresponding fusion/fragmentation and breakage kernels which must be accounted for correctly as many detailed features, revealed by the subsequent numerical simulations, depend non-linearly on these window sizes themselves. The details of how these window size constraints are handled are explained in the Appendix.…”
Section: Modelmentioning
confidence: 99%
“…If the breakage is also binary, it can be represented by an following overall function β ′ b (υ/υ ′ ) = 2/υ ′ . Other possibilities are a parabolic "U-shape" function for the daughter paricle size distribution (rigid particles are more likely to break into unequal pieces); considerable work in this area has been contributed by Coulaloglou and Tavlarides [34], Prince and Blanche [191] and Luo and Zvendsen [142] For analytical solutions to fragmentation problems, the reader may also consult Ziff and McGrady [268] or Ziff [267] and references within.…”
Section: Transport Equation With Collisions and Sourcesmentioning
confidence: 99%