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Mg5 CO3 4(OH)2·4H2O thermodynamically prefers to grow into the sheet-like crystal at the current solution growth environment, which has been successfully explained by using the chemical bonding theory.
In polypeptides and proteins, the phenomenon of conformational transitions has been successfully explained on the basis of Zimm and Bragg model, as a function of temperature, pressure, solvent concentration and pH etc.
The isotopic fractionation associated with the assimilations of CO2 and nitrate by photoautotrophs has been successfully explained with a two-step model (Figure 2a,b; Park and Epstein 1960; Wada and Hattori 1978; O'Leary 1981; Farquhar et al. 1982; Hayes 1991).
Cooperative oxygen binding has been successfully explained by the two-state model developed by Monod, Wyman and Changeux based on the structures of the T-state (tense, unligated) and R-state (relaxed, ligated) observed in hemoglobin crystals [7], [8], [9].
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In particular electrostatic interactions have been successfully explained by the use of the molecular electrostatic potential [2, 3].
Munekane et al. (2004) proposed a model in which the vertical movements are driven by the poroelastic deformations of the aquifer, and such movements have been successfully explained using this model.
The variations of the specific essential fracture work and specific plastic work with T and with ethylene content have been successfully explained in terms of the prevalent deformation mechanisms.
Although the observed properties of proton relaxation in homogeneous liquids such as pure water, ethanol, and glycerol have been successfully explained by the theory of Bloembergen, Purcell, and Pound (BPP) [1], the mechanism of water relaxation in more complex environments such as tissues is still highly speculative.
This model has been successfully used to explain the polarization behavior of natural sediments.
Even once a system has been successfully tested, Beste explains, it must be retested over and over.
A similar theory that is proposed because rupture and reformation of interfacial H-bond bridges has been successfully used to explain the variation of friction force versus ln[v] [29].
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