Sodium, relative weight

Pure sodium chloride, like pure water, has a definite melting (freezing) temperature (at a given pressure). Separating operations—such as distilling or freezing—do not separate the salt into components. The composition of the salt, whether expressed in relative numbers of sodium and chlorine atoms or in the relative weights of these atoms, is fixed and is represented by the formula NaCl. Sodium chloride, like water, is an example of a pure substance. 

The third possibility is that the molecular species is m/z 163 and that m/z 195 and m/z 217 are both adducts. If this is the case, it must be possible to explain the differences of 32 Da and 54 Da easily. Can this be done Commonly occurring adducts in electrospray involve the mobile phase and either sodium (relative molecular mass (RMM) 23) or potassium (RMM 39). The simplest interpretation of this spectrum is that the molecular weight of the analyte is 162, the ion at m/z 163 is the protonated species, that at m/z 195 is (M - - H - - CH30H)+ and that at m/z 217 is (M-h Na-h CH30H)+. Since the HPLC mobile phase contained methanol (molecular weight of 32), this is not an unreasonable conclusion. 

The relative weights of hexachloroplatinic acid to sodium nitrate used for fusion, f Each (1 wt% of Pt oxide) was added dissolved in a drop of water. 

Nondurable Finishes. Flame-retardant finishes that are not durable to launderiag and bleaching are, ia general, relatively iaexpensive and efficient (23). In some cases, a mixture of two or more salts is more effective than either of the components alone. For example, an add-on of 60% borax (sodium tetraborate) is required to prevent fabric from burning, and boric acid is iaeffective as a flame retardant even at levels equal to the weight of the fabric. However, a mixture of seven parts borax and three parts boric acid imparts flame resistance to a fabric with as Utde as 6.5% add-on. 

Acid—mordant dyes have characteristics similar to those of acid dyes which have a relatively low molecular weight, anionic substituents, and an affinity to polyamide fibers and mordant dyes. In general, brilliant shades caimot be obtained by acid—mordant dyes because they are used as their chromium mordant by treatment with dichromate in the course of the dyeing procedure. However, because of their excellent fastness for light and wet treatment, they are predominandy used to dye wool in heavy shades (navy blue, brown, and black). In terms of chemical constitution, most of the acid—mordant dyes are azo dyes some are triphenyhnethane dyes and very few anthraquinone dyes are used in this area. Cl Mordant Black 13 [1324-21 -6] (183) (Cl 63615) is one of the few examples of currentiy produced anthraquinone acid—mordant dyes. It is prepared by condensation of purpurin with aniline in the presence of boric acid, followed by sulfonation and finally by conversion to the sodium salt (146,147). 

Polybutene resins. These liquid resins are obtained by cationic polymerization of petroleum C4 streams in the presence of AICI3 at relatively low temperature. Temperature and AICI3 concentration are important factors as they influence the molecular weight and viscosity of the final resin. After reaction, the mixture is deactivated with water, methanol, ammonia or aqueous sodium hydroxide. The organic layer is separated and distilled to remove solvent and unconverted material. 

B. Standardisation against sodium tetraborate. The advantages of sodium tetraborate decahydrate (borax) are (i) it has a large relative molecular mass, 381.44 (that of anhydrous sodium carbonate is 106.00) (ii) it is easily and economically purified by recrystallisation (iii) heating to constant weight is not required (iv) it is practically non-hygroscopic and (v) a sharp end point can be obtained with methyl red at room temperatures, since this indicator is not affected by the very weak boric acid. 

Sodium chloride has a relative molecular mass of 58.44. A 0.1000M solution is prepared by weighing out 2.922 g of the pure dry salt (see Section 10.74) and dissolving it in 500 mL of water in a graduated flask. Alternatively about 2.9 g of the pure salt is accurately weighed out, dissolved in 500 mL of water in a graduated flask and the molar concentration calculated from the weight of sodium chloride employed. 

Successful NMP in emulsion requires use of conditions where there is no discrete monomer droplet phase and a mechanism to remove any excess nitroxide formed in the particle phase as a consequence of the persistent radical effect. Szkurhan and Georges"18 precipitated an acetone solution of a low molecular weight TEMPO-tcrminated PS into an aqueous solution of PVA to form emulsion particles. These were swollen with monomer and polymerized at 135 °C to yield very low dispersity PS and a stable latex. Nicolas et at.219 performed emulsion NMP of BA at 90 °C making use of the water-soluble alkoxyamine 110 or the corresponding sodium salt both of which are based on the open-chain nitroxide 89. They obtained PBA with narrow molecular weight distribution as a stable latex at a relatively high solids level (26%). A low dispersity PBA-WocA-PS was also prepared,... 

Deflocculants have a relatively low molecular weight. Polymers composed of sodium styrene sulfonate, maleic anhydride, and a zwitterionic functionalized maleic anhydride [738,1411,1412,1415] are suitable. 

In copolymers containing the styrene sulfonate moiety and maleic anhydride units, the maleic anhydride units can be functionalized with alkyl amine [1411-1416]. The water-soluble polymers impart enhanced deflocculation characteristics to the mud. Typically, the deflocculants are relatively low-molecular-weight polymers composed of styrene sodium sulfonate monomer maleic anhydride, as the anhydride and/or the diacid and a zwitterionic functionalized maleic anhydride. Typically the molar ratio of styrene sulfonate units to total maleic anhydride units ranges from 3 1 to 1 1. The level of alkyl amine functionalization of the maleic anhydride units is 75 to 100 mole-percent. The molar concentrations of sulfonate and zwitterionic units are not necessarily equivalent, because the deflocculation properties of these water-soluble polymers can be controlled via changes in their ratio. 

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