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Charge normal

Royalty is normally charged as a percentage of the gross revenues from the sale of hydrocarbons, and may be paid in cash or in kind (e.g. oil). The prevailing oil price is used. [Pg.309]

The commercial form of Cartesian manostat, model 7A, is depicted in Fig. II, 23, 7 it is normally charged with mercury except for very low pressures when di-w-butyl phthalate is employed. The manostat is highly sensitive in its action furthermore, once the pressure has been set in the instrument, the system may be shut down without disturbing the setting. [Pg.116]

Nonreacdive substances that can be used in small concentrations and that can easily be detected by analysis are the most useful tracers. When making a test, tracer is injected at the inlet of the vessel along with the normal charge of process or carrier fluid, according to some definite time sequence. The progress of both the inlet and outlet concentrations with time is noted. Those data are converted to a residence time distribution (RTD) that tells how much time each fracdion of the charge spends in the vessel. [Pg.2081]

The electrostatic force is directly proportional to the net charge of an aerosol particle. Therefore, effective charging of the particles is of great importance. Airborne particles are normally charged either due to their birth processes or due to charge transfer from gas ions to particles. The natural charging of particles is normally so weak that it has no practical importance for electrostatic air cleaning. [Pg.1213]

The water droplets from steam Jets are normally charged, and discharges sometimes occur from the Jets to neighboring grounded pipes. These discharges are of the corona type rather than true sparks and may be visible at night they look like small flames [2]. [Pg.293]

Electricity is normally charged for on the basis of power (kilowatts) and the supply authority must install plant whose rating (and therefore cost) is a function of the voltage of the system and the current which the consumer takes (i.e. kilo-volt-amps). The relationship between the two is kW = kVA x cos (j> where cos (j> is the power factor and is less than 1.0. In the case of loads which have a low power, factor the supply authority is involved in costs for the provision of plant which are not necessarily reflected in the kWh used. A penalty tariff may then be imposed which makes it economically worthwhile for the consumer to take steps to improve his power factor. Low power factors occur when the load is predominantly either inductive or capacitive in nature (as opposed to resistive). In most industrial circumstances where the load includes a preponderance of motors, the load is inductive (and the power factor is therefore lagging). Consequently, if the power factor is to be brought nearer to unity the most obvious method is to add a significant capacitive component to the load. [Pg.234]

Assuming that the material is ionic and the ions have their normal charges, Li+, Ni2+, O2-, the three compensation mechanisms possible for donor doping are ... [Pg.354]

FIGURE 1.25. Successive reversible electron transfers in cyclic voltammetry of attached reactants. Normalized charge (a) and current (b) as a function of the separation between the standard potentials, at 25°C, from right to left A ° — E — E = 0.4, 0.1, 0.0356, —0.2 V. The middle of each curve corresponds to — )/2. (c) Variation of the normalized peak current with AE° in the range where a single wave is observed. [Pg.66]

Consider now the case where the molecules A and B are free to move in the solution. Noting that the volume concentrations of the three reactants obey the same Nernst laws as in the attached reactants case, the preceding analysis may be used simply by replacing the normalized charge by the normalized convoluted current (as defined in Section 1.3.2), Thus,... [Pg.67]

Figure 1 Relationship of donor and acceptor molecules in charge transfer complexes (a) mixed stacks of alternating donor and acceptor molecules in a normal charge transfer complex (b) segregated stacks of donor and acceptor molecules in (TTF)(TCNQ) and related materials... Figure 1 Relationship of donor and acceptor molecules in charge transfer complexes (a) mixed stacks of alternating donor and acceptor molecules in a normal charge transfer complex (b) segregated stacks of donor and acceptor molecules in (TTF)(TCNQ) and related materials...
An additional point should be noted from table 3.3. Whereas the amino acid side chains (R groups) that are normally charged at physiological pH are restricted to five amino acids (aspartic acid, glutamic acid, lysine, arginine, and sometimes histidine), a number of potentially ionizable R groups are part of other amino acids. These include cysteine, serine, threonine, and tyrosine. The ionization reac-... [Pg.53]

Steam cracking of various petroleum fractions is gaining widespread use for the production of olefins. These olefins are produced essentially for use as feed stock for numerous petrochemical processes, but the by-product butylenes and propylenes are sometimes used as feed stock for aviation and motor alkylation units. Ethylene is the most important of the olefins produced from this type of cracking, and propylene is second in importance. These two olefins are normally charged to either alkylation or polymerization units for the production of petrochemicals or petrochemical intermediates. Polyethylene and propylene dimers, trimers, tetramers, and penta-mers are some of the more important polymers produced, while ethybenzene, dodecylbenzene, cumene, diisopropylbenzene, and alkylated... [Pg.169]

Fig. 4.3 Normalized charge-time curves foradouble potential step with Ei Fig. 4.3 Normalized charge-time curves foradouble potential step with Ei <S L° (()</[ < T[)...
The charge is a valuable magnitude for identifying the presence of homogeneous chemical reactions or, in general, deviations from a pure faradaic behavior. Thus, in absence of adsorption of redox species, the normalized charge-time curves can be written as... [Pg.247]

This equivalence between the charge of surface-bound molecules and the current of solution soluble ones is due to two main reasons first, in an electro-active monolayer the normalized charge is proportional to the difference between the total and reactant surface excesses ((QP/QP) oc (/> — To)), and in electrochemical systems under mass transport control, the voltammetric normalized current is proportional to the difference between the bulk and surface concentrations ((///djC) oc (c 0 — Cq) [49]. Second, a reversible diffusionless system fulfills the conditions (6.107) and (6.110) and the same conditions must be fulfilled by the concentrations cQ and cR when the process takes place under mass transport control (see Eqs. (2.150) and (2.151)) when the diffusion coefficients of both species are equal. [Pg.422]

The Qf E curve for a reversible two-electron transfer taking place in a monolayer is independent of time (i.e., it has a stationary character) and, therefore, is independent of the potential-time waveform applied to the electrode, as in the case of a reversible one-electron transfer reaction. It is also important to highlight that the normalized charge, has a identical expression to that for the normalized transient current 7 v N obtained for solution soluble species when the NPV technique is applied to an electrode with any geometry (see curves in Fig. 3.16, and Eq. (3.141)), and also to the normalized stationary current obtained for solution soluble species when any potential-time waveform is applied for ultramicroelectrodes with any geometry. [Pg.441]


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See also in sourсe #XX -- [ Pg.148 ]

See also in sourсe #XX -- [ Pg.408 ]




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Charging normal

Normal component of the electric field caused by a planar charge distribution

Normalized integral charge density

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