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Solutions normality

As noted earlier, control of the column s temperature is critical to attaining a good separation in gas chromatography. For this reason the column is located inside a thermostated oven. In an isothermal separation the column is maintained at a constant temperature, the choice of which is dictated by the solutes. Normally, the tern-... [Pg.568]

In packed beds of particles possessing small pores, dilute aqueous solutions of hydroly2ed polyacrylamide will sometimes exhibit dilatant behavior iastead of the usual shear thinning behavior seen ia simple shear or Couette flow. In elongational flow, such as flow through porous sandstone, flow resistance can iacrease with flow rate due to iacreases ia elongational viscosity and normal stress differences. The iacrease ia normal stress differences with shear rate is typical of isotropic polymer solutions. Normal stress differences of anisotropic polymers, such as xanthan ia water, are shear rate iadependent (25,26). [Pg.140]

Acetate and triacetate are essentially unaffected by dilute solutions of weak acids, but strong mineral acids cause serious degradation. The results of exposure of heat-treated and untreated triacetate taffeta fabrics to various chemical reagents have been reported (9). Acetate and triacetate fibers are not affected by the perchloroethylene dry-cleaning solutions normally used in the United States and Canada. Trichloroethylene, employed to a limited extent in the UK and Europe, softens triacetate. [Pg.294]

United States Pharmacopeia stronger ammonia water ammonia test solution normal (1 N) aqua ammonia chemically pure technical, Bh°... [Pg.357]

Although 16 different crystalline modifications have been identified (24,25), the a-pentahydrate is the stable form below 48°C. Solutions of sodium thiosulfate in the absence of seed crystals can be easily supercooled below their normal crystallisation temperatures. The dotted line extension of the dihydrate phase in Figure 1 is an indication that, if supercooling takes place below this line, solutions normally giving the pentahydrate may form the dihydrate [36989-90-9] s1ste2id. [Pg.28]

Component 1 is the solute, while component 2 is water. The molar volume of the solute in mVkmole is at the solute normal boiling point, while the viscosity of water in Pa sec is at the temperature of the system resulting in a diffusivity in mVsec. The average error is about 9 percent when tested on 36 experimental systems. [Pg.416]

Solutions normally tend to be random so that one cannot predict which of the sites will be occupied by which atoms (Fig. 2.2c). But if A atoms prefer to have A neighbours, or B atoms prefer B neighbours, the solution can cluster (Fig. 2.2d) and when A atoms prefer B neighbours the solution can order (Fig. 2.2e). [Pg.17]

Cleaning solutions normally use one or more of the following methods ... [Pg.154]

The last definition has widespread use in the volumetric analysis of solutions. If a fixed amount of reagent is present in a solution, it can be diluted to any desired normality by application of the general dilution formula V,N, = V N. Here, subscripts 1 and 2 refer to the initial solution and the final (diluted) solution, respectively V denotes the solution volume (in milliliters) and N the solution normality. The product VjN, expresses the amount of the reagent in gram-milliequivalents present in a volume V, ml of a solution of normality N,. Numerically, it represents the volume of a one normal (IN) solution chemically equivalent to the original solution of volume V, and of normality N,. The same equation V N, = V N is also applicable in a different context, in problems involving acid-base neutralization, oxidation-reduction, precipitation, or other types of titration reactions. The justification for this formula relies on the fact that substances always react in titrations, in chemically equivalent amounts. [Pg.330]

Nickel and nickel alloys possess good resistance to sea-water in conditions where the protective properties of the passive film are fully maintained. As pointed out above, Ni-30 Cu Alloy 400, in contrast to its behaviour in acidic solution, normally forms a protective film in neutral and alkaline environments, including sea-water this alloy and its age hardening variant... [Pg.787]

In the dilute aqueous solution normally used for measuring acidity, the concentration of water, H20], remains nearly constant at approximately 55.4 M at 25 °C. We can therefore rewrite the equilibrium expression using a new quantity called the acidity constant, Ka. The acidity constant for any acid HA is simply the equilibrium constant for the acid dissociation multiplied by the molar concentration of pure water. [Pg.50]

The a-bromoketone (non-enolizable on the a side) was treated with lithium hexamethyldisilazide (1 eq.) at -78 °C in THF, and then TMSCI (1 eq.) was added and the solution allowed to come to ambient temperature. It was then re-cooled to -78°C, and n-BuLi (2 eq.) was added, and the solution was allowed to come to ambient temperature. The mixture was poured into saturated ammonium chloride solution. Normal work-up and distillation gave the /3-ketosilane (50-80%). [Pg.49]

Nitroprusside infusion bottles are wrapped in aluminum foil or other opaque material to protect the drug from light. The administration tubing does not require a covering. If the solution is protected from light, it remains stable for up to 24 hours. The newly prepared solution normally has a very light brownish tint. The nurse should discard the solution if the mixture becomes blue, green, or dark red. [Pg.404]

The procedure for determination of neutral oils in AOS measures petroleum spirit-extractable material from an aqueous alcoholic solution. Normally a solution of 1 1 ethanol/water is used as to dissolve the sample prior to extraction. For higher molecular weight materials 2 1 propan-2-ol/water is preferred. The petroleum ether is removed on a steambath and finally under vacuum. The amount of neutral oil is then determined gravimetrically. Due to the slight volatility of alkenes, alkanes, and alcohols, especially in the C,2 materials, the neutral oil tends to be underestimated by these procedures. [Pg.440]

Figure 1.49. Change of the strontium content and Sr/ Sr ratio of Kuroko anhydrite during the deposition and dissolution due to the mixing of hot ascending solution and cold solution (normal seawater) (Shikazono et al., 1983). R mixing ratio (in weight) = S.W./(S.W.+H.S.) in which S.W. and H.S. are seawater and hydrothermal solution, respectively. Open triangle Fukazawa deposits. Solid triangle Hanawa deposits. Open square Wanibuchi deposits. Solid square Shakanai deposits. Concentration of Ca, Sr " " and SO of H.S. are assumed to be 1,(XX) ppm, 1 ppm, and 10 mol/kg H2O, respectively. Concentrations of Ca, Sr " and SO of S.W. are taken to be 412 ppm, 8 ppm, and 2,712 ppm. Temperatures of H.S. and S.W. are assumed to be 350°C and 5°C (Shikazono et al., 1983). Figure 1.49. Change of the strontium content and Sr/ Sr ratio of Kuroko anhydrite during the deposition and dissolution due to the mixing of hot ascending solution and cold solution (normal seawater) (Shikazono et al., 1983). R mixing ratio (in weight) = S.W./(S.W.+H.S.) in which S.W. and H.S. are seawater and hydrothermal solution, respectively. Open triangle Fukazawa deposits. Solid triangle Hanawa deposits. Open square Wanibuchi deposits. Solid square Shakanai deposits. Concentration of Ca, Sr " " and SO of H.S. are assumed to be 1,(XX) ppm, 1 ppm, and 10 mol/kg H2O, respectively. Concentrations of Ca, Sr " and SO of S.W. are taken to be 412 ppm, 8 ppm, and 2,712 ppm. Temperatures of H.S. and S.W. are assumed to be 350°C and 5°C (Shikazono et al., 1983).
Sodium hypochlorite is commercially available as an alkaline solution, normally containing the equivalent of 12-14% available chlorine. However, this is so unstable that analytical testing of its strength is always necessary before use. Calcium hypochlorite (bleaching powder), stabilised by adding lime, has been used in the past but this product is no longer used in textile bleaching. [Pg.132]

Acetic acid is generally not used as a complexant for Ni2+ in practical, e.g., commercially available, Ni-P solutions. Thus, the results obtained by Malecki and Micek-Hnicka [65, 68] may not apply to solutions normally employing a stronger complexant, e.g., citric acid, in acid-type electroless Ni-P solutions. However, the semi-quantitative approach used by these authors could serve as a model for the investigation of other kinds of electroless solutions. [Pg.243]

Liver tissue B12 is assayed by suspending 50 mg of lyophilized human liver in 100 ml of aconitate buffer to which 100 mg sodium metabisulfite is added. The suspension is autoclaved for 30 minutes at 16 psi to liberate the bound forms of the vitamin. Aliquots are diluted 1 10 after autoclaving to reduce metabisulfite toxicity on microorganism growth. Each milliliter now contains 50 pg of liver (w/v) 1.0, 1.5, and 2.0 ml of this hydrolyzate is added. After dilution to a volume of 5 ml, this represents an assay of 10, 15, and 20 ig of liver per milliliter of final solution. Normal liver contains between 2-14 mpg of vitamin B /mg liver powder. [Pg.233]

The printability of the LEP ink is determined by a number of factors, including the viscosity of the ink, the solvent evaporation rate, and the interactions between the ink and the screen, emulsion, and substrate. Screen-printable solutions normally require considerably... [Pg.575]

For solution-based analyses, it is normal to make up a set of synthetic standards from commercial calibration solutions (normally supplied as 1000 ppm stock solutions, e.g., from Aldrich, BDH, Fisons, or ROMIL). These are available to different degrees of purity, and it is necessary to use the level of purity commensurate with the sensitivity of the analytical technique to be used it is, however, better not to use the highest purity in all circumstances, since these are very expensive. Ideally each element to be determined in the sample should be calibrated against a standard solution containing that element, although interpolation is sometimes possible between adjacent elements in the periodic table, if some elements are missing. For most techniques, it is better to mix up a single standard solution... [Pg.306]

B4.2.4). The dotted lines correspond to Eq. (B4.2.5). Insert Steady-state fluorescence spectra of corresponding solutions normalized to the monomer emission (reproduced with permission from Atik et al., 1979b ). [Pg.88]

Salt type and concentration For back-extraction, increases in pH are not enough to strip the protein out from reverse micelles this is also due to the size exclusion elfect resulting from a decrease in the reverse micelle size [31,32]. This means that high salt concentration and salts that form small reverse micelles favor back transfer. Most of the work reported in the literature used KCl solution, normally 1.0 mol dm KCl coupled with a pH around 7.5. Marcozzi et al. [23] also showed that the back transfer efficiency of a-chymotrypsin depends on the salt type and concentration used in the forward transfer. [Pg.666]


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See also in sourсe #XX -- [ Pg.99 , Pg.100 ]




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Normal solution

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