Volume concentration and

The concentrate volume and plant location will tend to be the two major factors that determine the suitability of a particular option. The concentration of the brine is also important, as the severity of potential environmental impacts generally increases with increasing concentration. The siting of a desalination plant must take into account the availability of disposal options, along with potential sources of feed water for the plant and the proximity to the end user. [Pg.26]

Input values of concentration, volume, and moles are in cells B3 B6 in Figure 13-13. Cell B7 has the value 2 to indicate that glycine is a diprotic acid. Cell B8 has the activity coefficient of H+ computed with the Davies equation, 13-18. Cell B9 begins with the effec-... [Pg.264]

Changes in concentration, volume, and temperature make a difference in the amount of product formed in a reaction. Can a catalyst also affect product concentration A catalyst speeds up a reaction, but it does so equally in both directions. Therefore, a catalyzed reaction reaches equilibrium more quickly, but with no change in the amount of product formed. Read the Chemistry and Technology feature at the end of this chapter to learn how Le Chatelier s principle is applied to an important industrial process. [Pg.573]

Selectivity parameters, needed for the BOHLM or BAHLM module design and their determination techniques, are analyzed. Selectivity can be controlled by adjusting the concentration, volume, and flow rate of the LM phase. Such control of the selectivity is one of the advantages of the bulk liquid membrane systems in comparison with other liquid membranes configurations and Donnan dialysis techniques. The idea of dynamic selectivity and determination techniques are presented and discussed. [Pg.11]

Le Chatelier s principle allows us to predict the effects of changes in concentration, volume, and temperature on a system at equilibrium. This principle states that when a change is imposed on a system at equilibrium, the equilibrium position will shift in a direction that tends to compensate for the imposed change. [Pg.571]

The depth of a GA peel is a function of the concentration, volume, and duration of application. [Pg.131]

To apply Le Chatelier s principle, review the effects of concentration, volume, and temperature in the Chemical Principles section (pages 562-563). For each disturbance, predict how the reaction will change to counter the disturbance. [Pg.565]

We have seen that when a reaction reaches equilibrium, the rates of the forward and reverse reactions are equal and the concentrations remain constant. Now we will look at what happens to a system at equilibrium when changes occur in reaction conditions, such as changes in concentration, volume, and temperature. [Pg.454]

Animal tests have been extremely useful in the past to help manufacturers in the classification of their siufactants in terms of skin irritation potential, even if human and animal skin are not exactly the same. Methods have strongly evolved over the years toward methodologies more respectful of animal welfare lowering the concentration, volume, and surface of application of the test materials. A ban of animal testing for cosmetic products... [Pg.480]

The importance of treatment placement was evident in the earliest acid treatments. In his patent, Frasch noted the need for a ruhher packer for isolation, so that acid could be selectively injected into the formation. Although this need has been recognized from day one, the absence of proper acid placement is probably still the biggest reason why add jobs fail (besides improper well diagnosis). A well-conceived, properly designed treatment in all other aspects (formation damage assessment, selection of acid types, concentrations, volumes, and additives) can go for naught if the treatment is not properly placed. The zone of interest must be suffidently contacted by stimulation fluids. [Pg.96]

Z. Evaporation. If the wastewater is in low volume and the waste material involatile, then evaporation can be used to concentrate the waste. The relatively pure evaporated water might still require biological treatment after condensation. The concentrated waste can then be recycled or sent for further treatment or disposal. The cost of such operations can be prohibitively expensive unless the heat available in the evaporated water can be recovered. [Pg.313]

The equation is more conventionally written expressing the variable n/V as the inverse of the molar volume, l/v, although nJVis just the molar concentration c, and one could equally well write the equation as... [Pg.354]

Hydrolysis of Potassium Ethyl Sulphate. Dissolve about i g. of the crystals in about 4 ml. of cold distilled water, and divide the solution into two portions, a) To one portion, add barium chloride solution. If pure potassium ethyl sulphate were used, no precipitate should now form, as barium ethyl sulphate is soluble in water. Actually however, almost all samples of potassium ethyl sulphate contain traces of potassium hydrogen sulphate formed by slight hydrolysis of the ethyl compound during the evaporation of its solution, and barium chloride almost invariably gives a faint precipitate of barium sulphate. b) To the second portion, add 2-3 drops of concentrated hydrochloric acid, and boil the mixture gently for about one minute. Cool, add distilled water if necessary until the solution has its former volume, and then add barium chloride as before. A markedly heavier precipitate of barium sulphate separates. The hydrolysis of the potassium ethyl sulphate is hastened considerably by the presence of the free acid Caustic alkalis have a similar, but not quite so rapid an effect. [Pg.79]

IsoValeric acid. Prepare dilute sulphuric acid by adding 140 ml. of concentrated sulphuric acid cautiously and with stirring to 85 ml. of water cool and add 80 g. (99 ml.) of redistilled woamyl alcohol. Place a solution of 200 g. of crystallised sodium dicliromate in 400 ml. of water in a 1-litre (or 1-5 litre) round-bottomed flask and attach an efficient reflux condenser. Add the sulphuric acid solution of the isoamyl alcohol in amaU portions through the top of the condenser shake the apparatus vigorously after each addition. No heating is required as the heat of the reaction will suffice to keep the mixture hot. It is important to shake the flask well immediately after each addition and not to add a further portion of alcohol until the previous one has reacted if the reaction should become violent, immerse the flask momentarily in ice water. The addition occupies 2-2-5 hours. When all the isoamyl alcohol has been introduced, reflux the mixture gently for 30 minutes, and then allow to cool. Arrange the flask for distillation (compare Fig. II, 13, 3, but with the thermometer omitted) and collect about 350 ml. of distillate. The latter consists of a mixture of water, isovaleric acid and isoamyl isovalerate. Add 30 g. of potassium not sodium) hydroxide pellets to the distillate and shake until dissolved. Transfer to a separatory funnel and remove the upper layer of ester (16 g.). Treat the aqueous layer contained in a beaker with 30 ml. of dilute sulphuric acid (1 1 by volume) and extract the liberated isovaleric acid with two... [Pg.355]

Concentrate the combined filtrate and washings (W) to about half the original volume, and pour it into sUghtly more than the calculated amount of dilute hydrochloric acid (use a mixture of 30 ml. of concentrated hydrochloric acid and 30 ml. of ice-water) then add about 300 ml. of water. Collect the active aec.-octyl hydrogen phthalate (crude lA) as above (5). The weight of the air-dried ester is about half that of the dl-ester originally used (7). [Pg.507]

The sulphonanilldes may be prepared by either of the following methods —(i) Reflux the solution of the sulphonyl chloride in benzene obtained as above, with 2 5 g. of aniline for 1 hour. Concentrate the benzene solution to half its volume and cool in ice. Collect the solid which separates on a filter, wash with hot water, and recrystallise from ethanol or dilute ethanol. [Pg.553]

Method 2. Place a mixture of 126-5 g. of benzyl chloride, 76 g. of thiourea and loO ml. of rectified spirit in a 500 ml. round-bottomed flask fitted with a reflux condenser. Warm on a water bath. A sudden exothermic reaction soon occurs and aU the thiourea passes into solution. Reflux the resulting yellow solution for 30 minutes and then cool in ice. Filter off the white crystals and dry in the air upon filter paper. Concentrate the filtrate to half its original volume and thus obtain a further small crop of crystals. The yield of crude hydrochloric acid as in Method 1 the m.p. is raised to 150°, although on some occasions the form, m.p. 175°, separates. [Pg.966]

Molality is used in thermodynamic calculations where a temperature independent unit of concentration is needed. Molarity, formality and normality are based on the volume of solution in which the solute is dissolved. Since density is a temperature dependent property a solution s volume, and thus its molar, formal and normal concentrations, will change as a function of its temperature. By using the solvent s mass in place of its volume, the resulting concentration becomes independent of temperature. [Pg.18]

Commercially available concentrated hydrochloric acid is 37.0% w/w HCl. Its density is 1.18 g/mL. Using this information calculate (a) the molarity of concentrated HCl, and (b) the mass and volume (in milliliters) of solution containing 0.315 mol of HCl. [Pg.33]

A2.6540-g sample of an iron ore known to contain 53.51% w/w Fe is dissolved in a small portion of concentrated HCl and diluted to volume in a 250-mL volumetric flask. A spectrophotometric method is used to determine the concentration of Fe in this solution, yielding results of 5840, 5770, 5650, and 5660 ppm. Determine whether there is a significant difference between the experimental mean and the expected value at a = 0.05. [Pg.100]

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