Evaporation drawbacks

Reducing pH usually has a beneficial effect on corrosion caused by alkaline substances. However, this seemingly obvious solution has a number of drawbacks. Chemical treatment programs work most effectively in certain pH ranges. Decidedly acidic waters can cause corrosion problems as bad or worse, albeit different, than those caused by alkaline waters. Finally, if concentration mechanisms such as evaporation or condensation are present, merely decreasing pH may prove ineffective in controlling attack. 

Air conditioners are frequently combined with heaters. A convenient place must be found for the compressor, generally outdoors. Heat pumps have been used a great deal in recent years with satisfactory results. In very dry climates, laboratories often install evaporative coolers because of their reasonable cost of installation and operation. Their one drawback, sometimes serious, is that the inside air tends to become uncomfortably humid. 

C, is one of the most critical parameters in TSP operation, and should be optimised for different samples, wherever possible. This is considered to be a considerable drawback in routine operation of unknown polymer/additive extracts. Too low a vaporiser temperature results in the solute and solvent spraying into the ionisation source in their liquid form, without formation of gas-phase ions. Too high a vaporiser temperature causes premature evaporation of the solute and solvent before the outlet of the capillary is reached. This causes an unstable, pulsing ion beam. As ion formation in TSP operation depends very critically on the extent of desolvation and the energy of the nebulised droplets, it is clear that an inappropriate vaporiser temperature will cause loss of sensitivity. 

This success does, however, have a drawback the urea concentrations required could not possibly have existed in the primeval ocean. Thus, as in the case of other condensation reactions, one has to assume that there were ponds or lagoons, in which the necessary reagent concentrations could build up via evaporation of water. 

Despite the frequent use of arc-discharge and laser ablation techniques, both of these two methods suffer from some drawbacks. The first is that both methods involve evaporating the carbon source, which makes it difficult to scale up production to the industrial level using these approaches. Second, vaporization methods grow CNTs in highly tangled forms, mixed with unwanted forms of carbon and/or metal species. The CNTs thus produced are difficult to purify, manipulate, and assemble for building nanotube-device architectures in practical applications. 

A low value of L means a small cooling power, a serious drawback when cooling by evaporation. 

The fact that evaporated potassium arrives at the surface as a neutral atom, whereas in real life it is applied as KOH, is not a real drawback, because atomically dispersed potassium is almost a K+ ion. The reason is that alkali metals have a low ionization potential (see Table A.3). Consequently, they tend to charge positively on many metal surfaces, as explained in the Appendix. A density-of-state calculation of a potassium atom adsorbed on the model metal jellium (see Appendix) reveals that the 4s orbital of adsorbed K, occupied with one electron in the free atom, falls largely above the Fermi level of the metal, such that it is about 80% empty. Thus adsorbed potassium is present as K, with 8close to one [35]. Calculations with a more realistic substrate such as nickel show a similar result. The K 4s orbital shifts largely above the Fermi level of the substrate and potassium becomes positive [36], Table 9.2 shows the charge of K on several metals. 

Another important drawback involves the necessity to evaporate samples. Although at pressures of 10-5 to 10-6 torr and temperatures of 200 to 300°C many organic compounds evaporate, the method is unacceptable for thermolabile, polar, and high molecular weight compounds. 

Implementation of microanalytical devices presents some issues mostly related to the scale of the volumes. In fact, successive reduction in the sample volume may compromise analysis either because the measurement limit of the analytical method is exceeded or because the sample is no longer representative of the bulk specimen. Another drawback for microchip devices is microvolume evaporation of both sample and reagent from the microchip, compromising quantitative determination or inducing unwanted hydrodynamic flows. This problem has been addressed by designing pipetting systems that automatically replace fluid lost by evaporation or by enclosing the chip in a controlled... 

Technetiiun can also be isolated quantitatively from molybdate using Dowex-1 resin in the chloride form . Molybdate can be eluted with 0.1 M hydrochloride acid pertechnetate, however, is firmly adsorbed under these conditions. It can be readily eluted with 4.0 M nitric acid. The only drawback of this separation is the need to recover technetium from nitric acid solution. If the acid is evaporated with great care, losses may be kept quite low. 

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