Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

First solution

The acidity constant for an acid-base indicator was determined by preparing three solutions, each of which has a total indicator concentration of 5.00 X 10- M. The first solution was made strongly acidic with HCl and has an absorbance of 0.250. The second solution was made strongly basic and has an absorbance of 1.40. The pH of the third solution was measured at 2.91, with an absorbance of 0.662. What is the value of K, for the indicator ... [Pg.408]

First, solutes with larger electrophoretic mobilities (in the same direction as the electroosmotic flow) have greater efficiencies thus, smaller, more highly charged solutes are not only the first solutes to elute, but do so with greater efficiency. Second, efficiency in capillary electrophoresis is independent of the capillary s length. Typical theoretical plate counts are approximately 100,000-200,000 for capillary electrophoresis. [Pg.601]

The number of ways of placing the first solute molecule coi is proportional to the total volume of the solution V ... [Pg.554]

In this model we start with pure solvent so an undiminished value of V can be used for the first solute molecule. [Pg.554]

Arrhythmias. The first solution to cardiovascular problems arising from arrhythmias came about as a result of a complication caused by open-heart surgery. During procedures to correct congenital defects in children s hearts, the electrical conduction system often became impaired, and until it healed, the heart could not contract sufficiently without outside electrical stimulation. A system that plugged into a wall outlet was considered adequate until an electrical storm knocked out power, lea ding to the development of the first battery-powered external pacemaker. [Pg.181]

Liquid-liquid fractionation, or fractional extraction (Fig. 15-6), is a sophisticated scheme for nearly complete separation of one solute from a second solute by liquid-liquid extraclion. Two immiscible liquids travel countercurrently through a contaclor, with the solutes being fed near the center of the contactor. The ratio of immiscible-liquid flow rates is operated so that one of the phases preferentially moves the first solute to one end of the contactor and the other phase moves the second solute to the opposite end of the contactor. Another way to describe the operation is that a primaiy solvent S preferentially extracts, or strips, the first solute from the feed F and a wash solvent... [Pg.1449]

The capacity ratio of the first solute of the critical pair. [Pg.365]

This is simpler than the first solution but this approach is only convenient for the simple loading sequence of stress on-stress off. If this sequence is repeated many times then this superposition approach becomes rather complex. In these cases the analytical solution shown below is recommended but it should be remembered that the equations used were derived on the basis of the superposition approach illustrated above. [Pg.109]

One of the first solutions to the problem of stresses around an elliptical hole in an infinite anisotropic plate was given by Lekhnitskii [6-7]. A more recent and comprehensive summary of the problem and many others is Savin s monograph [6-8]. Numerous results by Lekhnitskii are shown in his books [6-9 and 6-10]. Two special cases are of particular interest. [Pg.336]

The simplest method of chromate sealing involves immersion in a dilute alkali chromate or dichromate solution followed by washing retained chromate imparts a yellow colour to the film. More substantial amounts of slightly soluble chromate can be deposited in the thicker type of absorbent anodic film by a method developed by Dr. L. Whitby at High Duty Alloys Ltd. In this, anodised parts are immersed first in a boiling 30% solution of sodium chromate and then in a boiling 2% solution of zinc nitrate. Residues of the first solution in the film react with the second solution to give a substantial yellow deposit of a basic zinc chromate, probably similar in composition to zinc yellow. [Pg.729]

If we put ni = w2 =. . =0 we find that u0, i o depend only on the properties of the solvent but wb ri depend on the properties both of the first solute and of the solvent, but do not depend on the other solutes, and so on. There is therefore an interaction between the molecules of the solvent and those of the solutes, but not between the latter themselves (cf. 129). When the solution is more concentrated, the interaction between solute molecules may be included by taking terms of higher order in the Taylor s... [Pg.364]

Thomas Edison was faced with the problem of measuring the electricity that each of his customers had used. His first solution was to use a zinc coulometer, an electrolytic cell in which the quantity of electricity is determined by measuring the mass of zinc deposited. Only some of the current used by the customer passed through the coulometer. (a) What mass of zinc would be deposited in 1 month (of 31 days) if... [Pg.645]

The next step is to put the first solution of the form (10) together with the second one of the form (9) the node i = i. The outcome of this is... [Pg.14]

Then each impurity was added to separate solutions of 1 g/dl polymeric dye so that the impurity concentrations were identical to those of the first solutions. This spiked dye was also chromatographed, and the two traces compared. [Pg.298]

As a further disadvantage, it is known concerning operation in many parallel micro channels that mixed flow patterns and even drying of the channels can occur [9, 10]. This comes from phase maldistribution to the channels. To overcome this problem, first solutions for phase equipartition have been proposed recently, but so far have not been applied for the mixers described here, but instead for mini-packed reactors, having feed sections similar to the mixers [11,12]. Nevertheless, numbering-up of dispersive-acting micro devices generally seems to be more complicated than for two-phase contactors (see Section 5.1.1). [Pg.581]

Adiponitrile is readily hydrogenated catalytically to hexamethylenediamine, which is an important starting material for the prodnction of nylons and other plastics. The electrochemical production of adiponitrile was started in the United States in 1965 at present its volume is about 200 kilotons per year. The reaction occurs at lead or cadmium cathodes with current densities of np to 200 mA/cm in phosphate buffer solutions of pH 8.5 to 9. Salts of tetrabntylammonium [N(C4H9)4] are added to the solution this cation is specihcally adsorbed on the cathode and displaces water molecules from the first solution layer at the snrface. Therefore, the concentration of proton donors is drastically rednced in the reaction zone, and the reaction follows the scheme of (15.36) rather than that of (15.35), which wonld yield propi-onitrile. [Pg.282]

Prepare a 40% solution of KI prepare a 1.7% solution of bismuth subnitrate in 20% acetic acid mix 5 ml of the first solution with 20 ml of the second solution add 75 ml of H2O spray the plates and warm Prepare a 0.2% solution of ninhydrin in n-butanol and add 3-ml acetic acid spray plates and heat for 3 to 5 min at 100 to 110°C... [Pg.316]

The first solution ESR spectra of the transient radicals were observed in 1969 and 1972. Silyl radicals see refs. 121a,c. Germyl radicals see ref 121a. Stannyl radicals ref. 97. [Pg.115]

The turbidity gradually increased as shown in Table 9.19, with an increase in the volume of solution or amount of CH3COONa in all samples (control, sonicated and boiled). But the increase in precipitation was not in proportion to the reagent added to the A12(S04)3 solution. The turbidity in the first solution for unsonicated, sonicated and boiled solution was roughly in the ratio 1 lVi 3. Turbidity in sonicated and boiled samples was almost equal in solution containing 10 ml of aluminium sulphate and 5.0 ml of sodium acetate. Turbidity in sonicated samples (10 + 10) increased marginally compared to the boiled sample. This trend of sonicated samples, as seen in Table 9.19, indicated the role of ultrasonic power to be important. When 20 ml of A12(S04)3 solution was mixed with 5 ml of sodium acetate and sonicated, the amount of precipitate formed was negligible compared to the precipitation in a mixture of 10 ml of A12(S04)3 and 2.5 ml of sodium acetate, where the intensity of the ultrasonic power was almost double. [Pg.256]

If the molecular effects of the electric field are irrelevant to microwave heating of solutions, this assumption could be envisaged in the use of operating conditions very far from current conditions. On one hand, it will be necessary to use an electric field of higher amplitude, or to reduce the temperature according to the Langevin function. This last solution is obviously antinomic with conventional chemical kinetics, and the first solution is, currently, technologically impossible. It will, on the other hand, be necessary to avoid reaction media with dielectric loss. The molecular effects of the microwave electric field could, paradoxically, be observed for a medium which is not heated by the action of microwave irradiation. [Pg.18]

In a second Schlenk tube were placed under nitrogen tert-butyl acetoacetate and dry 2-propanol (14 mL). The mixture was degassed and added to the first solution. Finally, degassed potassium 2-propylate solution (1 mL) was added. The resulting orange solution was stirred at room temperature. [Pg.122]

The design criteria for an in situ electrochemical STM include the above outlined considerations as well as several needs peculiar to an electrochemical environment. Sonnenfeld and Hansma (57) constructed the first STM to operate under solution. Their work highlights two important design considerations. Firstly, the tip and sample should be the only electrically active parts of the microscope exposed to solution. This first solution microscope was... [Pg.177]


See other pages where First solution is mentioned: [Pg.139]    [Pg.305]    [Pg.558]    [Pg.579]    [Pg.580]    [Pg.180]    [Pg.9]    [Pg.396]    [Pg.66]    [Pg.546]    [Pg.79]    [Pg.486]    [Pg.316]    [Pg.370]    [Pg.146]    [Pg.880]    [Pg.377]    [Pg.129]    [Pg.247]    [Pg.217]    [Pg.27]    [Pg.25]    [Pg.256]    [Pg.149]    [Pg.424]    [Pg.233]   
See also in sourсe #XX -- [ Pg.245 , Pg.254 ]




SEARCH



© 2024 chempedia.info