Water sodium perchlorate

Sodium dodecyl sulfate (SDS), 25% in water Lysozyme solution, 10 mg/mL in water Sodium perchlorate, 5 M Chloroform-isoamyl alcohol, 24 1 95% ethanol... 

Alkali solution (water, sodium perchlorate, sodium hydroxide, aniline, monochloric benzene, toluene diamine) 100 80 4-2 0.1 0.5... 

Ammonium perchlorate is a colorless, crystalline compound having a density of 1.95 g/mL and a molecular weight of 117.5. It is prepared by a double displacement reaction between sodium perchlorate and ammonium chloride, and is crystallized from water as the anhydrous salt. 

The alkah metal perchlorates are either white or colorless, and have increasing solubiUty in water in the order of Na > Li > NH4 > K> Rb > Cs. The high solubiUty of sodium perchlorate, NaClO, makes this material useful as an intermediate for production of all other perchlorates by double metathesis reactions and controlled crystallization. 

Ammonia, hydrochloric acid, and sodium perchlorate are mixed and the reaction mixture crystallised in a vacuum-cooled crystalliser. Ammonium perchlorate crystals are centrifuged, reslurried, recentrifuged, and then dried and blended for shipment. Mother Hquor is evaporated to precipitate sodium chloride and the depleted mother Hquor is recycled to the reactor. The AP product made by this method is 99% pure and meets the specifications for propeUant-grade ammonium perchlorate. The impurities are ammonium chloride, sodium perchlorate, ammonium chlorate, and water insolubles. 

The reseai ch has been carried out by the liquid chromatograph Perkin-Elmer (Series 200), which has tandem detectors the diode array (X=210 nm) and the refractometer. The temperature of a column was 30 C, speed of a mobile phase is 1.5 ml/ min. As a mobile phase, mixtures of solvents methanol - water and acetonitrile - water with addition of sodium perchlorate. The columns with the modified silica gel C8 and Cl8 (4.6x220 mm, 5 pm) were used for sepai ation of the AIST and FAS components. In order to make the identification of AIST and FAS components more reliable the ratio of the values of the above-mentioned detectors signals of each substance analyzed. 

Spray solution II Dissolve 92 mg potassium hydrogen phthalate in 100 ml water and adjust the pH to 5.0 with sodium hydroxide solution (1 mol/l). Dissolve 5 g sodium perchlorate in this solution [9]. 

The ionization eonstant should be a function of the intrinsic heterolytic ability (e.g., intrinsic acidity if the solute is an acid HX) and the ionizing power of the solvents, whereas the dissoeiation constant should be primarily determined by the dissociating power of the solvent. Therefore, Ad is expeeted to be under the eontrol of e, the dieleetrie eonstant. As a consequenee, ion pairs are not deteetable in high-e solvents like water, which is why the terms ionization constant and dissociation constant are often used interchangeably. In low-e solvents, however, dissociation constants are very small and ion pairs (and higher aggregates) become important species. For example, in ethylene chloride (e = 10.23), the dissociation constants of substituted phenyltrimethylammonium perchlorate salts are of the order 10 . Overall dissociation constants, expressed as pArx = — log Arx, for some substanees in aeetie acid (e = 6.19) are perchloric acid, 4.87 sulfuric acid, 7.24 sodium acetate, 6.68 sodium perchlorate, 5.48. Aeid-base equilibria in aeetie acid have been earefully studied beeause of the analytical importance of this solvent in titrimetry. 

With 77 % aqueous acetic acid, the rates were found to be more affected by added perchloric acid than by sodium perchlorate (but only at higher concentrations than those used by Stanley and Shorter207, which accounts for the failure of these workers to observe acid catalysis, but their observation of kinetic orders in hypochlorous acid of less than one remains unaccounted for). The difference in the effect of the added electrolyte increased with concentration, and the rates of the acid-catalysed reaction reached a maximum in ca. 50 % aqueous acetic acid, passed through a minimum at ca. 90 % aqueous acetic acid and rose very rapidly thereafter. The faster chlorination in 50% acid than in water was, therefore, considered consistent with chlorination by AcOHCl+, which is subject to an increasing solvent effect in the direction of less aqueous media (hence the minimum in 90 % acid), and a third factor operates, viz. that in pure acetic acid the bulk source of chlorine ischlorineacetate rather than HOC1 and causes the rapid rise in rate towards the anhydrous medium. The relative rates of the acid-catalysed (acidity > 0.49 M) chlorination of some aromatics in 76 % aqueous acetic acid at 25 °C were found to be toluene, 69 benzene, 1 chlorobenzene, 0.097 benzoic acid, 0.004. Some of these kinetic observations were confirmed in a study of the chlorination of diphenylmethane in the presence of 0.030 M perchloric acid, second-order rate coefficients were obtained at 25 °C as follows209 0.161 (98 vol. % aqueous acetic acid) ca. 0.078 (75 vol. % acid), and, in the latter solvent in the presence of 0.50 M perchloric acid, diphenylmethane was approximately 30 times more reactive than benzene. 

From this equilibrium it follows that 0.1 M sodium perchlorate will produce 6x10"5 M perchloric acid, i.e. sufficient to produce a significant acceleration for mercuration with mercuric acetate in the absence of added perchloric acid, but not otherwise. The acceleration of the rate of mercuration with mercuric perchlorate in 97 % aqueous acetic acid (but not with acetic acid containing a concentration of water of 0.2 M) was attributed to the fact that in the former... 

A mixture of water/pyridine appears to be the solvent of choice to aid carbenium ion formation [246]. In the Hofer-Moest reaction the formation of alcohols is optimized by adding alkali bicarbonates, sulfates [39] or perchlorates. In methanol solution the presence of a small amount of sodium perchlorate shifts the decarboxylation totally to the carbenium ion pathway [31]. The structure of the carboxylate can also support non-Kolbe electrolysis. By comparing the products of the electrolysis of different carboxylates with the ionization potentials of the corresponding radicals one can draw the conclusion that alkyl radicals with gas phase ionization potentials smaller than 8 e V should be oxidized to carbenium ions [8 c] in the course of Kolbe electrolysis. This gives some indication in which cases preferential carbenium ion formation or radical dimerization is to be expected. Thus a-alkyl, cycloalkyl [, ... 

The postulation of the +4 oxidation state of cobalt is necessary to account for the retarding influence of Pb(II). The existence of a dimeric species of Co(II) acetate is required by the rate law and is confirmed by spectrophotometric and solubility measurements. The existence of ionic species of the reactants is inferred by the rate increase on addition of sodium acetate, an observation which cannot be attributed to a salt effect because sodium perchlorate produces a rate decrease. On this scheme an explanation of the effect of water on the stoichiometry is that the step... 

Fig. 3. Circular dichroism at 15°C in water (solid line) and in 6 M sodium perchlorate (dashed line), (a) Ac-Ala-NHMe. (b) cyclo (-Ala-Ala-). (c) Ac-Ala-OMe. (d) Ac-Ala-Ala-OMe. (e) Ac-Ala-Ala-Ala-OMe. From Mattice (1974), Biopolymers 13, 169-183, 1974. Reprinted by permission of John Wiley 8c Sons, Inc.

Mixtures of the sulfoxide with metal salts of oxoacids are powerful explosives. Examples are aluminium perchlorate, sodium perchlorate and iron(III) nitrate [1], The water in hydrated oxosalts (aluminium perchlorate, iron(III) perchlorate, iron(III) nitrate) may be partially or totally replaced by dimethyl (or other) sulfoxide to give solvated salts useful as explosives [2], Metal nitrates and perchlorates solvated with DMSO are generally powerfully explosive, and under certain conditions a violent reaction is easily triggered [3], Several other explosions involving perchlorates and the sulfoxide have been reported. 

Annikov, V. E. et al., Chem. Abs., 1983, 99, 73190 MRH Acetone 4.89/18, ethanol 4.73/18, ethylene glycol 4.35/26 The detonation and combustion limits of mixtures of sodium perchlorate, water and ethylene glycol, glycerol, 1,3-butylene glycol, 2,3-butylene glycol, formamide, dimethylformamide, ethanolamine, diaminoethane, acetone, urea and galactose have been studied. 

This problem was resolved by Nakae et al. [7] using non-polar octadecylsilica as the stationary phase and a solution of 0.1 M of sodium perchlorate in methanol/water (80 20) as the mobile phase. The ternary system (water-alcohol-salt), previously used by Fudano and Konishi [8] as an eluent for the separation of ionic surfactants at higher concentrations, induced the so-called salting out effect . The addition of the organic solvent to the water modified the polarity of the eluent and produced a good separation within a short period of time [9]. It also has the function of dissociating the surfactant micelles in individual molecules that are dissolved in the eluent [8], The presence of the salt (NaC104) in the mobile phase has a considerable influence on... 

Figure 18 Positive- and negative-ion ESI mass spectra of ImM sodium perchlorate in methanol-water (50 50), at heated capillary of 220 C. [Reproduced from X. Zhao and J.Yinon, Rapid. Commun. Mass Spectrom., 16, (2002) 1137. Copyright 2002, with permission fromJohnWiley Sons].

The liquid chromatographic analysis was carried out using serial 4x300mm u-Bondagel E-125 and E-500 columns obtained from Waters Associates, Inc. The carrier was prepared to contain (A) 0.25M sodium perchlorate, 0.1% sodium lauryl sulfate that was dissolved and brought to pH 7.2 using ammonium phosphate and (B) tetrahydrofuran. An A/B ratio of 9 1 was mixed and filtered through a 0.2um membrane. 

Perchlorate is the oxidation product of chlorate. It forms a variety of compounds, including ammonium perchlorate, potassium perchlorate, sodium perchlorate, and perchloric acid. Perchlorate is highly reactive in its solid state, and as ammonium perchlorate it is used as the oxidizer in solid rocket fuel. Because of its limited shelf life, it must be periodically washed out of the country s rocket and missile inventory and replaced. Large volumes of the chemical have been disposed of since the 1950s, and perchlorate has been detected in large concentrations in both groundwater and surface water. Perchlorate has also been used in the manufacture of matches, munitions, fireworks, and in analytical chemistry. 

---