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Proportional diluters

If copper is known to be absent or present only in negligible proportions, dilute the solution with water to 50 mL in a graduated flask, and continue as detailed below. Otherwise, transfer the solution to a small separatory funnel and add 5 mL of the diethylammonium diethyldithiocarbamate in chloroform reagent (diluted 1 20 with chloroform when required). Shake and run off the chloroform layer, extract the aqueous layer with successive 1 mL portions of the reagent until the chloroform layer is colourless finally, wash the aqueous layer with a few mL of chloroform. Dilute the aqueous solution with water to 50 mL in a graduated flask. [Pg.696]

Figure 1. Example showing how proportional dilution may create compositional subgroups. Diluted specimens were created by multiplying 17 elemental concentrations in the nondiluted specimens by 0.66. Figure 1. Example showing how proportional dilution may create compositional subgroups. Diluted specimens were created by multiplying 17 elemental concentrations in the nondiluted specimens by 0.66.
Toxicant delivery systems are used to deliver, on a once-through basis, the various test concentrations to the test chambers in continuous-flow toxicity tests. The serial proportional diluter is the most common design used to mix the dilution water with the test substance to produce the desired test concentrations. The construction materials in toxicant delivery systems, like those for the test chambers, should not be rubber, certain plastics, or metallic materials. [Pg.2626]

Technically, the best method to ensure precise exposure and water quality is the use of a flow-through test methodology. A continuous-flow methodology usually involves the application of peristaltic pumps, flow meters, and mixing chambers to ensure an accurate concentration. Continuous flow methods are rarely used. The usual method is an intermittent flow using a proportional diluter (Figure 3.10) to mix the stock solution with diluent to obtain the desired test solutions. [Pg.45]

Schematic of a proportional diluter with flow controlled by solenoid valves. This mechanism ensures that an accurate concentration of the test material is reliably introduced to the test organisms at a specified rate. Schematic of a proportional diluter with flow controlled by solenoid valves. This mechanism ensures that an accurate concentration of the test material is reliably introduced to the test organisms at a specified rate.
This toxicity test is usually run as a static renewal, but some researchers have used a continuous flow setup with a proportional diluter. Handling the organisms during the transfer to new media is a potential problem for inexperienced technicians. [Pg.76]

Miscible with water in all proportions. Dilute solutions (<5%) are stable. Very strong acid. [Pg.671]

Percentages. Proportions Dilution of Solutions Indirect Proportions Molarity. Normality Specific Gravity. Density Baume (Bel Textile Terminology Peroxide... [Pg.230]

For this kind of case, a modification of the dilution method is being developed. Instead of using an external fixed-geometry measurement chamber, a suitable part of the process, e.g. a stretch of pipe, is used. A radiation detector is mounted on the outside of the pipe, and a tracer emitting sufficiently hard gamma radiation is used. As sufficient mixing can be achieved by injecting upstream the separator the radiation level found will be strictly proportional to the concentration and thus inversely proportional to the true flow rate. [Pg.1056]

Experiments on sufficiently dilute solutions of non-electrolytes yield Henry s laM>, that the vapour pressure of a volatile solute, i.e. its partial pressure in a gas mixture in equilibrium with the solution, is directly proportional to its concentration, expressed in any units (molar concentrations, molality, mole fraction, weight fraction, etc.) because in sufficiently dilute solution these are all proportional to each other. [Pg.360]

Place 1 0 g. of the monobasic acid and 2 g. of aniline or p-toluidine in a dry test-tube, attach a short air condenser and heat the mixture in an oil bath at 140-160° for 2 hours do not reflux too vigorously an acid that boils below this temperature range and only allow steam to escape from the top of the condenser. For a sodium salt, use the proportions of 1 g. of salt to 1 5 g. of the base. If the acid is dibasic, employ double the quantity of amine and a reaction temperature of 180-200° incidentally, the procedure is recommended for dibasic acids since the latter frequently give anhydrides with thionyl chloride. Powder the cold reaction mixture, triturate it with 20-30 ml. of 10 per cent, hydrochloric acid, and recrystallise from dilute alcohol. [Pg.362]

For many reductions it is not necessary to distil the reagent. Dilute the dark solution, prepared as above to the point marked with an asterisk, to 1 htre with dry isopropyl alcohol this gives an approximately one molar solution. Alternatively, prepare the quantity necessary for the reduction, using the appropriate proportions of the reagents. [Pg.883]

The nitric acid used in this work contained 10% of water, which introduced a considerable proportion of acetic acid into the medium. Further dilution of the solvent wnth acetic acid up to a concentration of 50 moles % had no effect on the rate, but the addition of yet more acetic acid decreased the rate, and in the absence of acetic anhydride there was no observed reaction. It was supposed from these results that the adventitious acetic acid would have no effect. The rate coefficients of the nitration diminished rapidly with time in one experiment the value of k was reduced by a factor of 2 in i h. Corrected values were obtained by extrapolation to zero time. The author ascribed the decrease to the conversion of acetyl nitrate into tetranitromethane, but this conversion cannot be the explanation because independent studies agree in concluding that it is too slow ( 5.3.1). [Pg.86]

According to Le Chatelier s principle, a system at equilibrium adjusts so as to mini mize any stress applied to it When the concentration of water is increased the system responds by consuming water This means that proportionally more alkene is converted to alcohol the position of equilibrium shifts to the right Thus when we wish to pre pare an alcohol from an alkene we employ a reaction medium m which the molar con centration of water is high—dilute sulfuric acid for example... [Pg.249]

The properties of several representative liquid-based ion-selective electrodes are presented in Table 11.3. An electrode using a liquid reservoir can be stored in a dilute solution of analyte and needs no additional conditioning before use. The lifetime of an electrode with a PVC membrane, however, is proportional to its exposure to aqueous solutions. For this reason these electrodes are best stored by covering the membrane with a cap containing a small amount of wetted gauze to... [Pg.483]

Figure 8.5 illustrates the sort of separation this approach predicts. Curve A in Fig. 8.5 shows the weight fraction of various n-mers plotted as a function of n. Comparison with Fig. 6.7 shows that the distribution is typical of those obtained in random polymerization. Curve B shows the distribution of molecular weights in the more dilute phase-the coacervate extract-calculated for the volumes of the two phases in the proportion 100 1. The distribution in the concentrated phase is shown as curve C it is given by the difference between curves A and B. [Pg.540]

For each of these phenomena in the limit of dilute solutions, some difference in the behavior of the solvent—Apj, ATf, or ATj,—is proportional to the mole fraction of the solute. Since the solutions are already assumed to be dilute, we note that... [Pg.543]

In the precoat and body feed mode, filter aids allow appHcation of surface filtration to clarification of Hquids, ie, filtration of very dilute suspensions of less than 0.1% by volume, such as those normally treated by deep bed filters or centrifugal clarifiers. Filter aids are used in this mode with pressure filters. A precoat is first formed by passing a suspension of the filter aid through the filter. This is followed by filtration of the feed Hquid, which may have the filter aid mixed with it as body feed in order to improve the permeabiUty of the resulting cake. The proportion of the filter aid to be added as body feed is of the same order as the amount of contaminant soHds in the feed Hquid this limits the appHcation of such systems to low concentrations. Recovery and regeneration of filter aids from the cakes normally is not practiced except in a few very large installations where it might become economical. [Pg.390]

Analyses of alloys or ores for hafnium by plasma emission atomic absorption spectroscopy, optical emission spectroscopy (qv), mass spectrometry (qv), x-ray spectroscopy (see X-ray technology), and neutron activation are possible without prior separation of hafnium (19). Alternatively, the combined hafnium and zirconium content can be separated from the sample by fusing the sample with sodium hydroxide, separating silica if present, and precipitating with mandelic acid from a dilute hydrochloric acid solution (20). The precipitate is ignited to oxide which is analy2ed by x-ray or emission spectroscopy to determine the relative proportion of each oxide. [Pg.443]

Ma.leic Anhydride. The largest chemical use for / -butane is as feedstock for maleic anhydride. A dilute air—butane mixture is passed over a vanadium—phosphoms catalyst 400—500°C to produce maleic anhydride [108-31-6] in good yield. Formerly benzene was used as feedstock, but in the last few years nearly all maleic anhydride in the United States, and an increasing proportion worldwide, is made from butane. [Pg.402]


See other pages where Proportional diluters is mentioned: [Pg.10]    [Pg.86]    [Pg.162]    [Pg.692]    [Pg.90]    [Pg.46]    [Pg.10]    [Pg.86]    [Pg.162]    [Pg.692]    [Pg.90]    [Pg.46]    [Pg.14]    [Pg.259]    [Pg.319]    [Pg.367]    [Pg.406]    [Pg.608]    [Pg.1364]    [Pg.1414]    [Pg.432]    [Pg.128]    [Pg.539]    [Pg.540]    [Pg.48]    [Pg.214]    [Pg.186]    [Pg.275]    [Pg.470]    [Pg.199]    [Pg.399]    [Pg.8]    [Pg.493]    [Pg.362]    [Pg.326]    [Pg.270]   
See also in sourсe #XX -- [ Pg.46 ]




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