Alkalies samples

In combustion mode, duplicate testa were carried out with a dry fuel feed rate of 0.33 g s" and an air factor of 1.6 (ratio of actual air-fuel ratio to the stoichiometric air-fuel ratio), Two tests were required to obtain alkali samples from both the disengagement section of the reactor and the cyclone stack. 

Alkali sampling location Combustion Mode Gasincation Mode ... 

Traces of ferric iron may contribute to the yellow color and for this reason Kenyon and Berwick (310) prefer to have tartaric acid present to form a less colored complex with iron. In analyzing caustic liquors they added varying amounts of sodium or potassium chloride, even though color is suppressed, because this permitted them to maintain a constant salt level when the alkali samples were neutralized with hydrochloric acid. 

Alkali-sampling probe apphed to characterize sorbents for a PFBC. 

On the other hand, relatively higher polymer loads accompanied increased concentration of alkaline treatment for bagasse ground to the same mesch size (samples 18 and 20 23 and 22) or grinding to finer particle size when treating with the same concentration of alkali (samples 18 and 19 21 and 22). Increased polymer load may relate to one or both of the following ... 

The thennal evaporation source was the earliest used to produce metal clusters in the gas phase [H, 12 and 13], mostly for clusters of the alkalis and other low melting point materials. In this technique, a bulk sample is simply... 

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. 

Suitable inlets commonly used for liquids or solutions can be separated into three major classes, two of which are discussed in Parts A and C (Chapters 15 and 17). The most common method of introducing the solutions uses the nebulizer/desolvation inlet discussed here. For greater detail on types and operation of nebulizers, refer to Chapter 19. Note that, for all samples that have been previously dissolved in a liquid (dissolution of sample in acid, alkali, or solvent), it is important that high-purity liquids be used if cross-contamination of sample is to be avoided. Once the liquid has been vaporized prior to introduction of residual sample into the plasma flame, any nonvolatile impurities in the liquid will have been mixed with the sample itself, and these impurities will appear in the results of analysis. The problem can be partially circumvented by use of blanks, viz., the separate examination of levels of residues left by solvents in the absence of any sample. 

Whereas the emission spectrum of the hydrogen atom shows only one series, the Balmer series (see Figure 1.1), in the visible region the alkali metals show at least three. The spectra can be excited in a discharge lamp containing a sample of the appropriate metal. One series was called the principal series because it could also be observed in absorption through a column of the vapour. The other two were called sharp and diffuse because of their general appearance. A part of a fourth series, called the fundamental series, can sometimes be observed. 

Germanium [7440-56-4] M 72.6, m 937 , 925-975 , b 2700 , d 5.3. Copper contamination on the surface and in the bulk of single crystals of Ge can be removed by immersion in molten alkali cyanide under N2. The Ge was placed in dry cyanide powder in a graphite holder in a quartz or porcelain boat. The boat was then inserted into a heated furnace which, after a suitable time, was left to cool to room temperature. At 750°, a 1mm thickness requires about Imin, whereas 0.5cm needs about half hour. The boat was removed and the samples were taken out with plastic-coated tweezers, carefully rinsed in hot water and dried in air [Wang J Phys Chem 60 45 7956]. 

The chemical resistance of PTFE is exceptional. There are no solvents and it is attacked at room temperature only by molten alkali metals and in some cases by fluorine. Treatment with a solution of sodium metal in liquid ammonia will sufficiently alter the surface of a PTFE sample to enable it to be cemented to other materials using epoxide resin adhesives. 

Other possibilities are the reduction of nitro groups by applying the sample solutions to adsorbent layers containing zinc dust and then exposing to hydrochloric acid vapors [110] 3,5-Dinitrobenzoates and 2,4-dinitrophenylhydrazones can also be reduced in the same way on tin-containing silica gel phases [111] Cellulose layers are also suitable for such reactions [112] Seiler and Rothweiler have described a method of trans-salting the alkali metal sulfates to alkali metal acetates [113]... 

Doping of alkali-metals into CNTs has been examined [11]. The X-ray powder diffraction (XRD) patterns of the K- or Rb-doped CNTs show that alkali-metals are intercalated between the CNT layers. The hexagonal unit cell is essentially the same as that of the stage-1 alkali-metal intercalated graphite ACg (A=K, Rb). For a sample doped with Rb, the observed lattice parameter of the perpendicular... 

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