Heat Transfer from Various Metal Surfaces

Heat Transfer from Various Metal Surfaces. 11-16... 

Heat Transfer from Various Metal Surfaces In an early work, Pridgeon and Badger [Jnd. Eng. Chem., 16, 474 (1924)] pubhshed test results on copper and iron tubes in a horizontal-tube evaporator that indicated an extreme effect of surface cleanliness on heat-transfer coefficients. However, the high degree of cleanhness needed for high coefficients was difficult to achieve, and the tube layout and... 

The inorganic deposits described in Tabie 1 of Chapter 1 usuaily are formed on the surfaces of heat transfer equipment such as power and waste-heat boilers and heat exchangers, and in the various parts of cooling water systems. Iron oxides, copper, and calcium-containing deposits make up the largest portion of the material that requires removal from the metallic surfaces. We will review major developments for the chemical removal of each category of scale. 

Thermal transmission testing is an excellent way of detecting various types of anomalies such as surface corrosion under paint before the corrosion becomes visually evident. Thin, single-layer structures, such as aircraft skin panels, can be inspected for surface and subsurface discontinuities. This test is simple and inexpensive, although materials with poor heat-transfer properties are difficult to test, and the joint must be accessible from both sides. For nonmetallic materials, the defect diameter must be on the order of 4 times its depth below the surface to obtain a reliable thermal indication. For metals, the defect diameter must be approximately 8 times its depth. Some bright surfaces such as bare copper and aluminum do not emit sufficient infrared radiation and may require a darkening coating on their surface. 

Also the mode of adsorption (e.g. of CO, hydrocarbons, etc.) can depend on the available ensemble size or given composition of the surface [64—68]. It appears that the heat of adsorption of various modes of CO adsorption is only marginally influenced when the required ensemble (1,2 or 3 and more) is transferred from a pure metal into a matrix of another metal (for instance alloys with Cu, Au and Ag). When a CO molecule, monitored by IR spectroscopy, is taken as a probe of the local electronic structure of atoms (or ensembles of atoms), no pronounced effects of alloying are found 69-71]. 

Atobe and Nonaka [67] have used a 20 kHz (titanium-alloy) sonic horn as the electrode (called sonoelectrode) for electroreductions of various benzaldehyde derivatives. This they did after insulating the submerged metal part of the horn-barrel with heat-shrink plastic. They found an improvement in current efficiency with insonation, but in addition noted some change in product selectivity towards one-electron-per-mole-cule products. Although the authors quote enhanced mass transfer across the electrode interface as the origin of the sonoelectrochemical trend towards products from the lesser amount of electrons per substrate molecule, the involvement of surface species on the reactive electrode provides a complication. 

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