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Low Potentials

Equations (1.23) and (1.25) give the following surface charge density-surface potential (cr-i/ o) relationship  [Pg.8]

Equation (1.26) has the following simple physical meaning. Since j/ decays from ij/o to zero over a distance of the order of (Eq. (1.25)), the electric field at the particle surface is approximately given by This field, which is generated by [Pg.8]


This particular sequence of conformations-trans bonds that advance the helix along the axis, alternating with gauche bonds which provide the twist-takes the chain through a series of relatively low potential energy states and generates a structure with minimum steric hindrance between substituents. If the polymer series is extended to include bulkier substituents, for example. [Pg.63]

In a world increasingly conscious of the dangers of contact with chemicals, a process that is conducted within the walls of a vacuum chamber, such as the VDP process for parylene coatings, offers great advantages. Provided the vacuum pump exhaust is appropriately vented and suitable caution is observed in cleaning out the cold trap (trace products of the pyrolysis, which may possibly be dangerous, would collect here), the VDP parylene process has an inherently low potential for operator contact with hazardous chemicals. [Pg.443]

Electron Transport Between Photosystem I and Photosystem II Inhibitors. The interaction between PSI and PSII reaction centers (Fig. 1) depends on the thermodynamically favored transfer of electrons from low redox potential carriers to carriers of higher redox potential. This process serves to communicate reducing equivalents between the two photosystem complexes. Photosynthetic and respiratory membranes of both eukaryotes and prokaryotes contain stmctures that serve to oxidize low potential quinols while reducing high potential metaHoproteins (40). In plant thylakoid membranes, this complex is usually referred to as the cytochrome b /f complex, or plastoquinolplastocyanin oxidoreductase, which oxidizes plastoquinol reduced in PSII and reduces plastocyanin oxidized in PSI (25,41). Some diphenyl ethers, eg, 2,4-dinitrophenyl 2 -iodo-3 -methyl-4 -nitro-6 -isopropylphenyl ether [69311-70-2] (DNP-INT), and the quinone analogues,... [Pg.40]

In a battery of tests, which determine the tendency of chemicals to inhibit aquatic organisms, accumulate in such organisms, and degrade in the environment, 2-hydroxy-2-nitro-l,3-propanediol was found to have low potential for harm in the environment (7). [Pg.61]

Vanillin has a low potential for acute and chronic toxicity, with a reported oral LD q in rats of 1580—3300 mg/kg. Dietary doses up to 20,000 ppm adrninistered to rats for two years resulted in no adverse toxicologic or carcinogenic effects. Vanillin is classified as a GRAS substance by EEMA. Consequently, at levels normally found in the human diet, vanillin would present no significant health or carcinogenic risk to humans. [Pg.401]

A low potential electron carrier, the fluorescent factor F420 [37333-48-5, 64885-97-8] (29) (it absorbs maximally at 420 nm), possessing a... [Pg.81]

The need for auxiliary heating is another factor that must be carefully evaluated. Due to the nature of the thermodynamic process, the gas discharging from an expander is at a much lower temperature than gas discharging from a regulator station operating within the same pressure bounds. If temperatures downstream of the expander are allowed to drop too low, potential problems may arise, such as hydrate formation and material compatibility. [Pg.479]

One criterion for the anode material is that the chemical potential of lithium in the anode host should be close to that of lithium metal. Carbonaceous materials are therefore good candidates for replacing metallic lithium because of their low cost, low potential versus lithium, and wonderful cycling performance. Practical cells with LiCoOj and carbon electrodes are now commercially available. Finding the best carbon for the anode material in the lithium-ion battery remains an active research topic. [Pg.343]

Low potential hazard A concentration of pollutants within a space, which will present a very low hazard to the occupants or the plant. [Pg.1456]

Although poloxamers show poor biodegradability, they exhibit very low acute toxicity [92] and are reported as having low potential for causing irritation and skin sensitization [26]. Toxicity decreases as ethylene oxide content increases, and the least toxic poloxamers are approved as food additives [80]. [Pg.773]

At high pH values and low potentials, Fe, Fe, Fe , Fe(OH)2 and Fe(OH)j, etc. will be thermodynamically unstable with respect to FeO H" and a further limited zone of corrosion will appear on the right-hand side of the diagram. [Pg.66]

Corrosion (in acid solutions) At low potentials iron will be oxidised to Fe and Fe203 reduced to Fe, and the a-p will be > 10" g ion/1 water will be reduced to hydrogen or remain stable, depending upon whether E is below or above curve/. At high potentials iron will be oxidised to Fe and Fe203 will dissolve to form Fe (Ef i /f 2 = 0-76 V) water will be stable or will be oxidised to oxygen, depending upon whether E is below or above curve m, respectively. [Pg.67]

It is worth emphasising too, that the position of those lines representing equilibria with the dissolved species, M, depend critically on the solubility of the ion, which is a continuous function of pH. For example, iron in moderately alkaline solution is expected to be very passive and so it is in borate solutions (in the absence of aggressive ions). However, the anodic polarization curve still shows a small active loop at low potential. [Pg.135]

The form of Figure 1.43 is common among many metals in solutions of acidic to neutral pH of non-complexing anions. Some metals such as aluminium and zinc, whose oxides are amphoteric, lose their passivity in alkaline solutions, a feature reflected in the potential/pH diagram. This is likely to arise from the rapid rate at which the oxide is attacked by the solution, rather than from direct attack on the metal, although at low potential, active dissolution is predicted thermodynamically The reader is referred to the classical work of Pourbaix for a full treatment of potential/pH diagrams of pure metals in equilibrium with water. [Pg.135]

The strains needed to initiate cracks in both the annealed and the sensitised materials were obtained using tapered slow-strain-rate specimens and the data are given in Fig. 8.36. As can be seen, there is little temperature dependence of the strain needed to initiate cracks in sensitised material whereas the annealed material was most susceptible to cracking at about 250°C. These results indicate the complicated response of Type 316 stainless steel to applied potential and demonstrate that, even though environmentally-assisted cracking may be generated by severe test methods, in this case the slow-strain-rate test, the results obtained must be used with care. For instance, the cracking of the annealed material at low potentials... [Pg.1221]

Coif balls high potential — - low potential energy energy... [Pg.157]

In general, the baser the metal, the lower (more negative) the electrical potential at the anode and the higher the potential rate of corrosion. Carbon steel and low-alloy steels (which are widely used in boiler plants) have a relatively low potential with respect to the standard hydrogen electrode and can therefore be expected to corrode readily unless active prevention measures are taken. Copper and brasses have a relatively higher potential. [Pg.150]

The consequences of these equations are seen in Figure 5.8 in which and are plotted against temperature at a fixed pressure. At the temperature T(h Ma = Mb and the two phases are in equilibrium. For T > To, ma > Mb and B is the stable phase. For T < To, /xB > and A is the stable phase. It can be seen from these relationships that n is a potential that drives the flow of mass in a phase change. Mass flows from the phase with high potential to the phase with low potential. When the two potentials are equal, equilibrium is established and there is no net flow of mass. [Pg.234]


See other pages where Low Potentials is mentioned: [Pg.80]    [Pg.251]    [Pg.361]    [Pg.55]    [Pg.87]    [Pg.84]    [Pg.84]    [Pg.161]    [Pg.353]    [Pg.155]    [Pg.321]    [Pg.73]    [Pg.1102]    [Pg.111]    [Pg.132]    [Pg.532]    [Pg.532]    [Pg.574]    [Pg.928]    [Pg.943]    [Pg.1165]    [Pg.1189]    [Pg.1221]    [Pg.353]    [Pg.359]    [Pg.512]    [Pg.248]    [Pg.304]    [Pg.402]    [Pg.78]    [Pg.237]    [Pg.219]   


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Alternative Measures of Oxidation Potential in Low Temperature Environments

Large-amplitude potential step low coverage

Low Potential Case

Low-potential electrode

Low-potential iron-sulfur proteins

Reduction at low potential

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