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Oxidation measuring susceptibility

Both NH3 oxidizers and N02 oxidizers, but especially the former, are susceptible to inhibition by a wide range of compounds, and several different modes of action have been documented (Bedard and Knowles, 1989). The two most common modes of inhibition are (1) interference with the active site of the primary enzyme (i.e., NH3 monooxygenase in AOB N02 oxidoreductase in NOB) by compounds that share structural homology with NH3 or N02 and (2) metal binding compounds, which interfere with the action or availability of copper in the NH3-oxidizing enzymes. In both NH3- and N02 -oxidizers, the susceptibility to inhibitors by key enzymes forms the basis of some methods used to measure the rate of nitrification in the environment (see above). [Pg.236]

In order to measure susceptibility to oxidation without the need to isolate the lipoproteins, methods have been developed for oxidizing whole serum or plasma and measuring diene formation (R2, S4). Such approaches may be subject to error as a result of variation in other oxidizable plasma components such as bilirubin, albumin, fibrinogen, and uric acid. A method that uses heparin affinity chromatography to separate LDL and intermediate density lipoproteins (IDL) from other serum proteins was described by Vinson et al. (V3, V5) and was later better standardized (K3). This approach has been shown to reflect susceptibility to oxidation in animal and human plasma under a variety of conditions (K3, V5). The heparin separation procedure is detailed in the following text. [Pg.15]

Corrosion protection of metals can take many fonns, one of which is passivation. As mentioned above, passivation is the fonnation of a thin protective film (most commonly oxide or hydrated oxide) on a metallic surface. Certain metals that are prone to passivation will fonn a thin oxide film that displaces the electrode potential of the metal by +0.5-2.0 V. The film severely hinders the difflision rate of metal ions from the electrode to tire solid-gas or solid-liquid interface, thus providing corrosion resistance. This decreased corrosion rate is best illustrated by anodic polarization curves, which are constructed by measuring the net current from an electrode into solution (the corrosion current) under an applied voltage. For passivable metals, the current will increase steadily with increasing voltage in the so-called active region until the passivating film fonns, at which point the current will rapidly decrease. This behaviour is characteristic of metals that are susceptible to passivation. [Pg.923]

Molecular Weight. Measurement of intrinsic viscosity in water is the most commonly used method to determine the molecular weight of poly(ethylene oxide) resins. However, there are several problems associated with these measurements (86,87). The dissolved polymer is susceptible to oxidative and shear degradation, which is accelerated by filtration or dialysis. If the solution is purified by centrifiigation, precipitation of the highest molecular weight polymers can occur and the presence of residual catalyst by-products, which remain as dispersed, insoluble soHds, further compHcates purification. [Pg.343]

COD provides i measure of the oxygen equivalent to that portion of the organic mtitter in i sample that is susceptible to oxidation by a strong chemical oxidant. A higher level of COD can be degraded (neutralized) chemically. The le el of COD. however, automatically reduces with the level of BOD and no further treatment is normally necessary. [Pg.417]

Surface active agents are important components of foam formulations. They decrease the surface tension of the system and facilitate the dispersion of water in the hydrophobic resin. In addition they can aid nucleation, stabilise the foam and control cell structure. A wide range of such agents, both ionic and non-ionic, has been used at various times but the success of the one-shot process has been due in no small measure to the development of the water-soluble polyether siloxanes. These are either block or graft copolymers of a polydimethylsiloxane with a polyalkylene oxide (the latter usually an ethylene oxide-propylene oxide copolymer). Since these materials are susceptible to hydrolysis they should be used within a few days of mixing with water. [Pg.797]

There are some aspects in the raw dry NR grades for adhesive manufacturing to be considered. NR tends to suffer oxidative degradation catalyzed by metals (mainly copper). The susceptibility of NR to oxidation can be measured using the plasticity retention index. The better grades of rubber have the higher plasticity retention index. [Pg.582]

Electrobalances suitable for thermogravimetry are readily adapted for measurements of magnetic susceptibility [333—336] by the Faraday method, with or without variable temperature [337] and data processing facilities [338]. This approach has been particularly valuable in determinations of the changes in oxidation states which occur during the decompositions of iron, cobalt and chromium oxides and hydroxides [339] and during the formation of ferrites [340]. The method requires higher concentrations of ions than those needed in Mossbauer spectroscopy, but the apparatus, techniques and interpretation of observations are often simpler. [Pg.31]

Lithium oxides of Pu, magnetic measurements and reciprocal molar susceptibility vs. [Pg.464]

Experimental evidence in humans is based upon intervention studies with diets enriched in carotenoids or carotenoid-contaiifing foods. Oxidative stress biomarkers are measured in plasma or urine. The inhibition of low density lipoprotein (LDL) oxidation has been posmlated as one mechanism by which antioxidants may prevent the development of atherosclerosis. Since carotenoids are transported mainly via LDL in blood, testing the susceptibility of carotenoid-loaded LDL to oxidation is a common method of evaluating the antioxidant activities of carotenoids in vivo. This type of smdy is more precisely of the ex vivo type because LDLs are extracted from plasma in order to be tested in vitro for oxidative sensitivity after the subjects are given a special diet. [Pg.179]

In this paper the use of Mfissbauer spectroscopy and magnetic susceptibility to measure the size of supported oxide catalyst... [Pg.528]

Si(Pc)0] (S04)o.09)n> i-s limited by the oxidative stability of the sulfate anion. Thermoelectric power, optical reflectivity, magnetic susceptibility, and four-probe electrical conductivity measurements evidence behavior typical of an [Si(PcP+)0]n compound where p 0.20. That is, there is no evidence that the more concentrated counterion charge has induced significant localization of the band structure. [Pg.233]

This is a relatively hard theory to test. It requires an experimental manipulation of susceptibility to oxidative stress in males, preferably both upward and downward, coupled with measurements... [Pg.492]


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See also in sourсe #XX -- [ Pg.15 ]




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Oxidation susceptibility

Oxidative measurement

Oxidative susceptibility

Oxidized measurement

Susceptibility measurements

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