Since the process using two reactive gases is much more complex than one reactive gas, the transition zone of the reactive mode must be defined taking into account oxygen and nitrogen mass flow rates.
This is because preventive strategies are more complex in nature than reactive ones, and are often riddled with unintended consequences.
Some applications require more complex processing of multiple reactive objects and data, that when placed inside render* braces significantly slow the application's re-evaluation of the output.
Evidently, gene and phenotype networks can be much more complex, as the causal-reactive genes may be also interacting in a broader network through an intricate cascade of genes and phenotypic traits.
While paracetamol is a very small molecule with few polar sites, the same principle can be applied in reasoning out highly reactive sites in more complex molecules.
A more complex dual continuum 2D/3D pore-scale reactive transport model including a modified diffusivity/porosity relationship and possibly complex precipitation kinetics (e.g. heterogeneous nucleation and inhibition processes) may provide a better description.
More complex syntheses are required for more reactive or highly functionalized leaving groups, such as protected nucleotides, i.e., pHP ATP (24, X = ATP), pHP GTP, and O-labeled isotopomers of pHP GTP.
By contrast, two other reports suggested that the relationship between iron deficiency and reactive thrombocytosis is more complex than a mere consequence of a crossreactivity between erythropoietin and thrombopoietin [ 35, 36].
The design, operation and control of reactive distillation columns are more complex than those involved for either reactors or conventional distillation columns.
The design and operation issues for reactive distillation systems are considerably more complex than those involved for either conventional reactors or conventional distillation columns.
