Milliliters , 33 table

The table below gives the weight in grams X 10 of 1 mL of air at 760 mm of mercury pressure and at the temperature indicated. Density in grams per milliliter is the same as the specific gravity referred to water at 4°C as unity. To convert to density referred to air at 70°F as unity, divide the values below by 12,00,... 

The following factors are the equivalent of the milliliter of normal alkali. Where the normality of the solution being used is other than normal, multiply the factors given in the table below by the normality of the solution employed. 

VOLUME.dat Section 1.1.2 A set of five precision weighings of a water-filled 100 ml flask the weights in grams were converted to milliliters using the standard density-vs.-temperature tables. Use with MSD to test the effect of truncation errors on the calculation of the standard deviation. (See Table 1.1.)... 

ELECTRODEjcls Fig. 4.24 The operation of an ion-specific electrode with a slope of 59.16 mV per decade for mono-valent ions (29.58 mV/dec for di-valent ions) is simulated under the assumption that a digital volt meter with a resolution of, say, 0.1 mV is used. The sample volume and the concentration of the metered titration solution are known. Normally, one would add a few milliliters of the concentrated titration solution and do the calculation spelled out in lines 140-150 in Table 4.22 here, because the sample concentration is known, the result can be normalized to it. The operation of short-cuts (volume correction), unknowns (volume bias, deviation of true slope from theoretical), and equipment shortcomings (digitization) can be studied. 

The values reported In Table III represent readings taken after incubation times of 24 hr for all organisms except M. smegmatis. which was read at 72 hr. The concentration of the tube of highest dilution that was free from growth was recorded as the minimum inhibitory concentration (micrograms per milliliter). 

Table III - Minimum Inhibitory Concentration (Micrograms per Milliliter) of Active Compounds...

The volumes of isotonic solutions prepared in milliliters from a gram of selected drug substances are listed in Table 8.3. 

TABLE 8.3. Volume of Isotonic Solutions Prepared (in Milliliters) from 1 g of Drug Substance. 

The next step is to determine the practical detection limit (pDL) based on the signal-to-noise ratio at the lowest level at which the analyst can get the HPLC system to function reproducibly on injections of a standard at a known concentration (S/N ratio of 3 1 is a rule of thumb). Then the practical quantitation limit (pQL) is determined usually at a level 2-5 times the pDL and the repeatability of the standard at this level is determined. This pQL usually results in analyte concentrations of nanograms or micrograms per milliliter. The repeatability of a 1.0 pg/mL clarithromycin standard preparation is shown in Table 2. ... 

An immunization scheme for rabbits is given in Table 4.5. Do not forget to take some milliliters of blood for pre-immun serum immediately before or after the first immunization. 

L. You must determine the correct pathway to get from gallons to liters using the conversions provided in Table 2-3. To do so, convert from gallons to cups, then to milliliters, and finally to liters ... 

Solve these kinds of problems by using the definition of molarity and conversion factors. In parts (b) and (c), you must first convert your mass in grams to moles. To do so, you divide by the molar mass from the periodic table (flip to Chapter 7 for details). In addition, be sure you convert milliliters to liters. 

TABLE 1. REPRESENTATIVE CONSTITUENTS OF HUMAN BLOOD (VALUES ARE PER 100 MILLILITERS)... 

The recommended technique for determination of abrasion pH is to grind, in a nonreactive mortar, a small amount of the mineral in a few drops of water for about one minute. Usually, a pH test paper is used. Values obtained in this manner are given in the left-hand column of the accompanying table. Another method, proposed by Keller etal. in 1963 involves the grinding of 10 grains of crushed mineral m 100 milliliters of water and noting the pH of the resulting slurry electronically. 

The amount of active enzyme associated with a given enzyme preparation is typically reported as units of activity per milliliter, units of activity per milligram, or units of activity per milligram protein. The latter expression (units/mg protein) is referred to as the preparation s specific activity (Segel, 1975). Measured specific activities for the peptidase preparation employed in this experiment are given in Table C2.2.1. Notice that values calculated from data... 

Plotting the pH data in Table 16.1 as a function of milliliters of NaOH added gives the pH titration curve in Figure 16.6b (page 678). This curve exhibits a gradual increase in pH in the regions before and after the equivalence point but a very... 

The solubility of a solid in a liquid is the amount of the solid that will dissolve in the liquid to form an equilibrated saturated solution (Faure, 1998), 111. In the literature, the solubility of a particular solid substance in water has been traditionally derived from laboratory measurements of the mass or moles of the solid that dissolves in a given mass or volume of distilled and deionized water. These values are often listed in milligrams per liter, grams per 100 milliliters (Lide, 2007), grams per liter, micrograms per liter Oigl-1), molal, molar, or micromolar ( iM) (Table 2.8). 

The accuracy of BE-AES measurements is directly related to the accuracy with which a solution concentration can be determined. ICP-AES, requires milliliter quantities of sample to accurately determine a concentration. However, the technique is sensitive to low micromolar concentrations of most elements. The high analyte concentrations obtained during the final concentrating step are necessary for maximizing the difference in concentrations between the two buffer chambers and as such must be diluted prior to ICP-AES concentration determination. Table 18.1 indicates approximate concentrations and volumes present during buffer equilibration and ICP-AES concentration determination. Unless otherwise noted, concentrations are the actual concentration in the buffer equilibrium step prior to dilution for ICP-AES measurement. 

Fifty milliliters of a solution of succinic acid in medium was equilibrated overnight with a known amount of sorbent ( 5 g) in a manner similar to that in Table 1. Resins were regenerated in hot water at 90°C and capacities calculated using dry weights. 

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