1994
DOI: 10.1016/0009-2509(94)e0052-r
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Unsteady processes of combined polymerization and crystallization in continuous apparatuses

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Cited by 51 publications
(32 citation statements)
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“…Non-stationary contributions entering in the growth rates of spherical particles, their radii, and the distribution of temperature and concentration fields must be taken into account in the theoretical description of the intermediate stage of phase transformation in melts and solutions (the analytical description of crystal growth in dilute solutions is presented in appendix A). For this reason, many theories of growth of crystals or droplike aggregates in supersaturated solutions, supercooled melts, mushy layers, colloids, magnetic fluids and other physical systems (see, among others, [18][19][20][21][22][23][24][25][26][27]) should be reconsidered with allowance for the non-stationary contributions to the particle growth rates.…”
Section: Discussionmentioning
confidence: 99%
“…Non-stationary contributions entering in the growth rates of spherical particles, their radii, and the distribution of temperature and concentration fields must be taken into account in the theoretical description of the intermediate stage of phase transformation in melts and solutions (the analytical description of crystal growth in dilute solutions is presented in appendix A). For this reason, many theories of growth of crystals or droplike aggregates in supersaturated solutions, supercooled melts, mushy layers, colloids, magnetic fluids and other physical systems (see, among others, [18][19][20][21][22][23][24][25][26][27]) should be reconsidered with allowance for the non-stationary contributions to the particle growth rates.…”
Section: Discussionmentioning
confidence: 99%
“…Estimating β 2 * ∆t/(aΛ) ∼ 10 −2 t s −1 as a typical case for metallic melts, we conclude that the second term in expressions (18) becomes substantial at times t 10 s after nucleation of a certain particle. In other words, the commonly used approximation of the particle growth rate V(t) ≈ β * ∆ [13,14,22,[26][27][28][29] is only the rough estimate that describes the main contribution only. In order to obtain a more precise description of the real nucleation process one can use next terms in the asymptotic expansion of R(t) and V(t) found in expressions (18).…”
Section: Unsteady-state Growth Rate Of Spherical Nucleimentioning
confidence: 99%
“…At the concluding stage, the growth of each particle influences the evolution of neighbouring crystals so that Ostwald ripening, coagulation and fragmentation processes are capable of occurring [13][14][15][16][17]. Let us especially note that such processes as external electromagnetic fields [18], buoyancy forces [19], polymerization [9,20] and withdrawal mechanisms of product crystals from a crystallizer [21][22][23][24] may essentially change the dynamics of particulate assemblages in a metastable liquid as well.…”
Section: Introductionmentioning
confidence: 99%