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Rates increases

There can be an element of maintenance costs that is fixed and an element which is variable. Fixed maintenance costs cover routine maintenance such as regular maintenance on safety valves which must be carried out irrespective of the rate of production. There also can be an element of maintenance costs which is variable. This arises from the fact that certain items of equipment can need more maintenance as the production rate increases. Also, royalties which cover the cost of purchasing another company s process technology may have different bases. Royalties may be a variable cost, since they can sometimes be paid in proportion to the rate of production. Alternatively, the royalty might be a single-sum payment at the beginning of the project. In this case, the single-sum payment will become part of the project s capital investment. As such, it will be included in the annual capital repayment, and this becomes part of the fixed cost. [Pg.406]

As the discount rate increases then the NPV is reduced. The following diagram shows the cashflow from the previous example (assuming an oil price of 20/bbl and ignoring the effect of inflation) at four different mid-year discount rates (10%, 20%, 25%, 30%). [Pg.322]

Breslow studied the dimerisation of cyclopentadiene and the reaction between substituted maleimides and 9-(hydroxymethyl)anthracene in alcohol-water mixtures. He successfully correlated the rate constant with the solubility of the starting materials for each Diels-Alder reaction. From these relations he estimated the change in solvent accessible surface between initial state and activated complex " . Again, Breslow completely neglects hydrogen bonding interactions, but since he only studied alcohol-water mixtures, the enforced hydrophobic interactions will dominate the behaviour. Recently, also Diels-Alder reactions in dilute salt solutions in aqueous ethanol have been studied and minor rate increases have been observed Lubineau has demonstrated that addition of sugars can induce an extra acceleration of the aqueous Diels-Alder reaction . Also the effect of surfactants on Diels-Alder reactions has been studied. This topic will be extensively reviewed in Chapter 4. [Pg.26]

This reaction showed certain characteristics which distinguish it from nitrations in solutions of nitric acid in organic solvents. Thus, in changing the solvent from carbon tetrachloride to nitromethane, the rate increased by a factor of only 6, whereas nitration involving the nitronium ion was accelerated by a factor of about 30 when the solvent was changed from acetic acid to nitromethane. It was held that the... [Pg.52]

The dependence of the zeroth-order rate constants on the concentration of acetyl nitrate is shown in fig. 5.1 in the absence of added acetic acid the rate increases according to the third power of the concentration of acetyl nitrate, but when acetic acid is added the dependence becomes... [Pg.87]

The theoretical curve, deduced from the kinetic expression of the mechanism, fits the experimental points with gratifying exactness, whereas, for pD>12, the simple mechanism reported earlier (428,430) becomes predominant, and the rate increases very rapidly with pD and becomes first order both in thiazole and deuteroxide concentrations (Fig. [Pg.118]

Rate increases with increasing po larity of solvent as measured by its dielectric constant e (Section 8 12) Polar aprotic solvents give fastest rates of substitution solvation of Nu IS minimal and nucleophilicity IS greatest (Section 8 12)... [Pg.356]

Steel is an acceptable material of constmction for handling solutions of up to 50% NaOH below 40°C. Above 40°C the steel corrosion rate increases rapidly and iron is picked up in the solution. Materials for handling 50% NaOH are lined steel for tank cars and lined or unlined steel for tanks and piping. [Pg.515]

For given operating conditions and submergence, the dry cake production rate increases with the speed of rotation (eq. 10) and the limiting factor is usually the minimum cake thickness which can stiU be successfiiUy discharged by the method used in the filter. Equation 11 shows the dependence of the sohds yield on cake thickness ... [Pg.393]

C. Above this temperature, the shear stress at constant shear rate increases and the rheological exponent rises from 0.25 toward 0.5 at the final melting point (68). [Pg.350]

Properties. Xanthan gum is a cream-colored powder that dissolves in either hot or cold water to produce solutions with high viscosity at low concentration. These solutions exhibit pseudoplasticity, ie, the viscosity decreases as the shear rate increases. This decrease is instantaneous and reversible. Solutions, particularly in the presence of small amounts of electrolyte, have exceUent thermal stabiHty, and their viscosity is essentially constant over the range 0 to 80°C. They are not affected by changes in pH ranging from 2 to 10. [Pg.436]

The quahtative flow distribution in a manifold can be estimated by examining a streamline plot. Figure 13 shows the streamline plot for the manifold having AR = 4. Note that the same amount of fluid flows between two consecutive streamlines. The area ratio is an important parameter affecting the flow distribution in a manifold, as shown in Figure 14a, which shows the percent flow rate in each channel for three cases. As the area ratio increases, the percent flow rate increases in channels no. 1 and no. 8, whereas the percent flow rate decreases in the middle channels. [Pg.497]

HMnO 2H20 [24653-70-1] decomposes at 18°C. Aqueous solutions of permanganic acid below a concentration of 3 wt % are stable over time, whereas in the concentration range of 5—15% HMnO, the decomposition rate increases with increasing initial solution concentration at room temperature (103). [Pg.515]

The kinetics of the reaction are relatively slow and permanganate solutions exhibit greatest stabiUty around a neutral pH. The decomposition rates increase below pH 3 or above pH 10. Potassium permanganate solutions are stable at elevated temperatures, up to approximately 3 N sodium hydroxide, above which decomposition into manganate occurs. [Pg.516]

A faster cooling rate increases dendrite nuclei formation, resulting in smaller dendrites. Small dendrites produce a microstmcture that is easier to homogenize during sintering. The finer the constituents, the more uniform the properties of the powder. [Pg.180]

Stress corrosion cracking, prevalent where boiling occurs, concentrates corrosion products and impurity chemicals, namely in the deep tubesheet crevices on the hot side of the steam generator and under deposits above the tubesheet. The cracking growth rates increase rapidly at both high and low pH. Either of these environments can exist depending on the type of chemical species present. [Pg.194]

The variety of designs in use for MRFs in the United States results in different quality products. As recycling rates increase, new facilities are buUt. For glass separation, the foUowing devices are typically utilized. [Pg.570]

Sulfur. Low sulfur stocks and EV sulfur-accelerated systems have better aging resistance. Normally, the oxidation rate increases with the amount of sulfur used in the cure. The increased rate may be due to activation of adjacent C—H groups by high levels of combined sulfur. Saturated sulfides are more inert to oxidation than aHyUc sulfides. Polysulfidic cross-links impart excessive hardening of SBR as compared to more stable monosulfidic cross-links. [Pg.246]

Viscosity. Sedimentation rate increases with decreased viscosity, )J., and viscosity is dependent on temperature. Often mineral oils, which are highly viscous at room temperature, have a viscosity that is reduced by a factor of 10 at 70—80°C. Tar, soHd at room temperature, is a low viscosity Hquid at 150—200°C and can be clarified of inorganic soHds at high flow rates. Even the viscosity of water changes significantly when the temperature changes between 10 and 35°C (10). [Pg.402]

Hydrolysis of TEOS in various solvents is such that for a particular system increases directiy with the concentration of H" or H O" in acidic media and with the concentration of OH in basic media. The dominant factor in controlling the hydrolysis rate is pH (21). However, the nature of the acid plays an important role, so that a small addition of HCl induces a 1500-fold increase in whereas acetic acid has Httie effect. Hydrolysis is also temperature-dependent. The reaction rate increases 10-fold when the temperature is varied from 20 to 45°C. Nmr experiments show that varies in different solvents as foUows acetonitrile > methanol > dimethylformamide > dioxane > formamide, where the k in acetonitrile is about 20 times larger than the k in formamide. The nature of the alkoxy groups on the siHcon atom also influences the rate constant. The longer and the bulkier the alkoxide group, the lower the (3). [Pg.251]


See other pages where Rates increases is mentioned: [Pg.83]    [Pg.1939]    [Pg.2098]    [Pg.2421]    [Pg.2478]    [Pg.3047]    [Pg.80]    [Pg.265]    [Pg.140]    [Pg.36]    [Pg.548]    [Pg.151]    [Pg.311]    [Pg.411]    [Pg.412]    [Pg.53]    [Pg.54]    [Pg.480]    [Pg.384]    [Pg.236]    [Pg.424]    [Pg.339]    [Pg.455]    [Pg.160]    [Pg.118]    [Pg.348]    [Pg.508]    [Pg.526]    [Pg.89]    [Pg.439]    [Pg.228]   
See also in sourсe #XX -- [ Pg.389 , Pg.617 ]




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