Science and Technology of Crystal Growth 1995
DOI: 10.1007/978-94-011-0137-0_6
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Topics in Crystal Growth Kinetics

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Cited by 28 publications
(25 citation statements)
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“…Similar values for the kinetic coefficient were found for the crystallization of several other macromolecules [31,[36][37][38]. The lower values of b for macromolecular crystallization compared with inorganic crystallization [35] has been attributed to the necessity of the pre-kink selection of the proper orientation of an incoming macromolecule for incorporation into the growth step [28]. At lower supersaturation a non-linear dependency of tangential step rate was observed (Fig.…”
Section: Surface Morphology and Growth Step Kinetics Of Glucose Isomesupporting
confidence: 70%
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“…Similar values for the kinetic coefficient were found for the crystallization of several other macromolecules [31,[36][37][38]. The lower values of b for macromolecular crystallization compared with inorganic crystallization [35] has been attributed to the necessity of the pre-kink selection of the proper orientation of an incoming macromolecule for incorporation into the growth step [28]. At lower supersaturation a non-linear dependency of tangential step rate was observed (Fig.…”
Section: Surface Morphology and Growth Step Kinetics Of Glucose Isomesupporting
confidence: 70%
“…where O ¼ 4:8 Â 10 À19 is the specific volume of a glucose isomerase tetramer in the crystal, c and c e ¼ 2:1 Â 10 15 cm À3 are initial and equilibrium concentrations of protein, respectively, and b is the step kinetic coefficient [35]. From the linear portion of vðc À c e Þ dependencies for ðc À c e Þ > 10 14 cm À3 (Fig.…”
Section: Surface Morphology and Growth Step Kinetics Of Glucose Isomementioning
confidence: 99%
“…The figure of merit for the discussion here is the net growth of two molecules for 128 s, leading to an average net flux (j ϩ Ϫ j Ϫ ) ϭ 0.054 s Ϫ1 into the growth sites distributed with mean density n k Ϫ1 ϭ 0.28. Because there are no sources or sinks of molecules at the step other than the attachment sites, the step growth rate v should equal an k Ϫ1 (j ϩ Ϫ j Ϫ ) (7,12). At (C͞C e Ϫ 1) ϭ 1, at which all data in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…For the kinetics of the phase transitions in solutions, it is generally accepted that colloid particles follow the diffusion-limited model, whereas the growth rates of new phases of small molecules are thought to be governed by a transition state (3)(4)(5)(6)(7). For the intermediate case of protein solid phases, the growth kinetics largely resemble those of small molecules, and it was assumed that transition-state laws apply (8).…”
mentioning
confidence: 99%
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