For the cross-linking system, the kinetics was characterized by the universal gelation mechanism, namely: (1) divergence of the slow mode and (2) appearance of the power law in ICF around the gelation threshold regardless of the polymerization method.
For a carbonate system, the kinetics of reaction between CO2 and formation water is as follows (Omole and Osoba 1983): Open image in new window Fig. 5 Permeability versus distance from inlet (at So = 79%%) Open image in new window Fig. 6 Permeability versus distance from inlet (at So = 30%%).
For the current model system, the kinetics of the solid-phase system can be estimated based upon enzyme loading per surface area (i.e., concentration) and flow rates.
In the absence of endogenous STAT3 in this system, the kinetics of Tyr phosphorylation of FLAG STAT3α or FLAG STAT3β could also be defined.
The effects of different catalyst systems on the kinetics of the "click" polymerization were evaluated by differential scanning calorimetry (DSC) and oscillatory rheology.
It should be noted that this change in color did not occur immediately as reported in other systems; instead, the kinetics were rather slow.
Since the purpose of our modeling is not to produce a model but to produce an exploratory and explanatory tool, we focus on systems where the kinetics of individual reactions or transporters have been well-studied experimentally.
In terms of absolute number, the values are not comparable between different systems (ultrasound machines) or different settings of a same system, but the kinetics of these values are respected.
The results show that in both systems the local kinetics of these processes strongly depend on the polarization conditions.
