Growth efficiency composition dependence

The chemical reaction mechanism of electropolymerization can be described as follows. The first step in course of the oxidative electropolymerization is the formation of cation radicals. The further fate of this highly reactive species depends on the experimental conditions (composition of the solution, temperature, potential or the rate of the potential change, galvanostatic current density, material of the electrode, state of the electrode surface, etc.). In favorable case the next step is a dimerization reaction, and then stepwise chain growth proceeds via association of radical ions (RR-route) or that of cation radical with a neutral monomer (RS-route). There might even be parallel dimerization reactions leading to different products or to the polymer of a disordered structure. The inactive ions present in the solution may play a pivotal role in the stabilization of the radical ions. Potential cycling is usually more efficient than the potentiostatic method, i.e., at least a partial reduction... 

For the identical experimental conditions, electroporation efficiency depends on the type of cells the composition of the membrane, shape, and size of cells strongly influences the electroporation efficiency [40-42]. In electroporation of bacteria, the growth phase of cell has significant influence on transformation efficiency, which is higher for cells harvested and electroporated from mid-log phase. However, cells from stationary phase can also be transected with reasonably good efficiency. Mammalian cell can be electroporated at relatively lower fields but pulse length controls the entry of external molecules into cells. 

As one of its major interests, a model represents an efficient tool for the kinetic analysis of cellular processes. It is able to account for the main phenomena that may simultaneously control the activities of cells. As such, depending on the culture conditions, composition of the medium and whether there is batch or continuous mode of operation, it can be used first to identify the rate-limiting factors and then to characterize quantitatively their relative importance. For instance, with a model it is possible to evaluate the kinetic effect of a depletion of glucose, glutamine and other amino acids or of an accumulation of ammonia and lactate on the rates of cell growth and death. 

Not only is there a need for the characterization of raw bulk materials but also the requirement for process controled industrial production introduced new demands. This was particularly the case in the metals industry, where production of steel became dependent on the speed with which the composition of the molten steel during converter processes could be controlled. After World War 11 this task was efficiently dealt with by atomic spectrometry, where the development and knowledge gained about suitable electrical discharges for this task fostered the growth of atomic spectrometry. Indeed, arcs and sparks were soon shown to be of use for analyte ablation and excitation of solid materials. The arc thus became a standard tool for the semi-quantitative analysis of powdered samples whereas spark emission spectrometry became a decisive technique for the direct analysis of metal samples. Other reduced pressure discharges, as known from atomic physics, had been shown to be powerful radiation sources and the same developments could be observed as reliable laser sources become available. Both were found to offer special advantages particularly for materials characterization. 

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