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Derivative formation, surface

To gain additional information about the chemical nature of surface groups several methods involving the formation of derivatives of surface groups have been developed ... [Pg.296]

Since the first report on a copper(II) Pc adlayer on Cu(100) [178], several studies describing the formation of Pc adlayers in air, in ultra-high vacuum (UHV), or at the solid-liquid interface have been reported [179-183], most of them involving the use of scanning tunneling microscopy (STM), a widely used technique for studying the organization of Pc derivatives on surfaces. [Pg.25]

It appears that a karst surface formed soon after the Belden Shale was removed. After the Leadville was exposed, a main, lower branch to the cave, and a high-water overpass into the Formation Room were formed. The cave stream carried limestone and chert gravel and cobbles derived from surface exposures of the Leadville Limestone and from material eroded from the cave walls. [Pg.119]

For Co/Al2C>3 the yield of C2 and C3 hydrocarbons relative to Cj was greatest at the highest temperature examined. The TPC study showed that this catalyst had a very low coking rate, associated with the well dispersed Co° derived from surface Co2+ ions. Here, the FT polymerisation synthesis does not have to compete with coke formation, therefore a higher selectivity towards higher hydrocarbons is achieved. [Pg.514]

Effect of two plasticizers (DBP - dibutyl phthalate and DD - a mixture of dioxane derivatives) on surface stress has been compared (Figure 11.41). Surface stress is useful in understanding the effect of plasticizer on the critical concentration of micelle formation and the potential stability of water dispersion of stabilizer. [Pg.324]

Poor Signal-to-Noise Ratio - The sample current is only a fraction of the total signal. The majority of the signal for Mode II detections is derived from surface oxide formation. Oxide-formation signal tends to be noisy. [Pg.93]

In addition to the studies of DNA assembly on surfaces a particular focus for hydrogen-bonding studies has been the use of the individual DNA bases to create self-assembled structures on surfaces. " The assembly of guanine and its derivatives on surfaces has received particular attention in part because of interest in the formation of guanine... [Pg.3733]

High quahty SAMs of alkyltrichlorosilane derivatives are not simple to produce, mainly because of the need to carefully control the amount of water in solution (126,143,144). Whereas incomplete monolayers are formed in the absence of water (127,128), excess water results in facile polymerization in solution and polysiloxane deposition of the surface (133). Extraction of surface moisture, followed by OTS hydrolysis and subsequent surface adsorption, may be the mechanism of SAM formation (145). A moisture quantity of 0.15 mg/100 mL solvent has been suggested as the optimum condition for the formation of closely packed monolayers. X-ray photoelectron spectroscopy (xps) studies confirm the complete surface reaction of the —SiCl groups, upon the formation of a complete SAM (146). Infrared spectroscopy has been used to provide direct evidence for the hiU hydrolysis of methylchlorosilanes to methylsdanoles at the soHd/gas interface, by surface water on a hydrated siUca (147). [Pg.537]

Run-of-the-mill instruments can achieve a resolution of 5-10 nm, while the best reach 1 nm. The remarkable depth of focus derives from the fact that a very small numerical aperture is used, and yet this feature does not spoil the resolution, which is not limited by dilfraction as it is in an optical microscope but rather by various forms of aberration. Scanning electron microscopes can undertake compositional analysis (but with much less accuracy than the instruments treated in the next section) and there is also a way of arranging image formation that allows atomic-number contrast, so that elements of different atomic number show up in various degrees of brightness on the image of a polished surface. [Pg.225]

Participation in the electrode reactions The electrode reactions of corrosion involve the formation of adsorbed intermediate species with surface metal atoms, e.g. adsorbed hydrogen atoms in the hydrogen evolution reaction adsorbed (FeOH) in the anodic dissolution of iron . The presence of adsorbed inhibitors will interfere with the formation of these adsorbed intermediates, but the electrode processes may then proceed by alternative paths through intermediates containing the inhibitor. In these processes the inhibitor species act in a catalytic manner and remain unchanged. Such participation by the inhibitor is generally characterised by a change in the Tafel slope observed for the process. Studies of the anodic dissolution of iron in the presence of some inhibitors, e.g. halide ions , aniline and its derivatives , the benzoate ion and the furoate ion , have indicated that the adsorbed inhibitor I participates in the reaction, probably in the form of a complex of the type (Fe-/), or (Fe-OH-/), . The dissolution reaction proceeds less readily via the adsorbed inhibitor complexes than via (Fe-OH),js, and so anodic dissolution is inhibited and an increase in Tafel slope is observed for the reaction. [Pg.811]

This view of the corrosion process is, however, more often than not too simplified an explanation. First, even when general corrosion take place (as in an idle or wet lay-up boiler), the reaction mechanisms tend to occur at many localized points on the boiler metal surface, typically where cracks and other imperfections in the magnetite film exist. Second, such processes almost always lead to derived forms of localized corrosion, which often result in severe metal wastage through the formation of deep pits. [Pg.245]

Other common poly glycol-based antifoams include certain derivatives of polyethylene glycol (PEG), which are condensation polymers of ethylene glycol. An example is polyethylene glycol-8 dioleate. Apart from its antifoam properties, PEG-8 dioleate is also used in cooling water inhibitor formulations as a surface cleaner, in the formation of a corrosion-inhibiting surface film. Additionally, it is employed as an oil-soluble emulsifier for other defoamer chemistries. [Pg.553]


See other pages where Derivative formation, surface is mentioned: [Pg.286]    [Pg.302]    [Pg.4896]    [Pg.263]    [Pg.454]    [Pg.185]    [Pg.156]    [Pg.356]    [Pg.376]    [Pg.163]    [Pg.191]    [Pg.297]    [Pg.322]    [Pg.258]    [Pg.537]    [Pg.540]    [Pg.545]    [Pg.293]    [Pg.344]    [Pg.25]    [Pg.141]    [Pg.143]    [Pg.254]    [Pg.288]    [Pg.1158]    [Pg.738]    [Pg.808]    [Pg.819]    [Pg.425]    [Pg.440]    [Pg.167]    [Pg.278]    [Pg.714]    [Pg.48]    [Pg.57]   


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Derivative formation, surface groups, minerals

Derivatives, formation

Derived surface

Formate derivatives

Surface formation

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