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Surface activation nitrate

The quantity dyl3 In a2 at the potential of the electrocapillary maximum is of basic importance. As the surface charge of the electrode is here equal to zero, the electrostatic effect of the electrode on the ions ceases. Thus, if no specific ion adsorption occurs, this differential quotient is equal to zero and no surface excess of ions is formed at the electrode. This is especially true for ions of the alkali metals and alkaline earths and, of the anions, fluoride at low concentrations and hydroxide. Sulphate, nitrate and perchlorate ions are very weakly surface active. The remaining ions decrease the surface tension at the maximum on the electrocapillary curve to a greater or lesser degree. [Pg.222]

An attempt to combine electrochemical and micellar-catalytic methods is interesting from the point of view of the mechanism of anode nitration of 1,4-dimethoxybenzene with sodinm nitrite (Laurent et al. 1984). The reaction was performed in a mixture of water in the presence of 2% surface-active compounds of cationic, anionic, or neutral nature. It was established that 1,4-dimethoxy-2-nitrobenzene (the product) was formed only in the region of potentials corresponding to simultaneous electrooxidation of the substrate to the cation-radical and the nitrite ion to the nitrogen dioxide radical (1.5 V versus saturated calomel electrode). At potentials of oxidation of the sole nitrite ion (0.8 V), no nitration was observed. Consequently, radical substitution in the neutral substrate does not take place. Two feasible mechanisms remain for addition to the cation-radical form, as follows ... [Pg.255]

Micellar catalytic methods were used to operate a choice between these two mechanisms. When an ion-radical has a charge opposite to that of the micelle surface, it is trapped by the micelle (Okamoto et al. 2001). In the presence of a surface-active compound, the aromatic substrate is nitrated in the very depth of a micelle, and the reaction rate depends on the local concentration of the nitrating agent on phase boundaries between the micelle and solution. A positively charged... [Pg.255]

Gelatin-Dynomite Containing Surface Active Agents. Triethanolamine oleate 0.1 is. added to NG 21 and NC 0.5 at 120°F then a blend of AN 14.1, Na nitrate 49.1, carbonaceous combustible material 9.0, sulfur 6 chalk 0.3 parts is added... [Pg.692]

Chretien and Woringer [34] described the preparation of silver cyanamide from calcium cyanamide by the action of silver nitrate and also described its explosive properties. Montagu-Pollock [35] described a method for growing large crystals of the salt from its aqueous solution in the presence of ammonium nitrate, ammonia and a surface active agent. Bowden and Montagu-Pollock [36] and Montagu-Pollock [35] studied the slow decomposition of the crystals when heated at temperatures from 150 to 360°C. The course of decomposition was studied by electron microscope. [Pg.211]

Recently Hino and Yokogawa [59] found that by adding less than 1% surface active agents, an improvement of transmission of detonation of ammonium nitrate explosives can be achieved. [Pg.423]

According to Hino and Yokogava [59] an addition of surface active agents (0.5-1 %) to mixtures of ammonium nitrate with liquid coal-tar improves the trans-... [Pg.436]

To a medium having a composition of 6.4 % of millet jelly, 0.5 % of glucose, 3.5 % of soybean powder, 0.75 % of corn steep liquor, 0.3 % of sodium chloride, 0.1 % of potassium secondary phosphate, 0.05 % of zinc sulfate, 0.01 % of copper sulfate, 0.2 % of sodium nitrate and 0.01 % of Toho No. 1 (trade name for a surface active agent composed of polyoxyethylene manufactured by Toho Chemical Industry Co. Ltd., Japan) was added 3-amino-propyl-dimethylsulfonium bromide hydrobromate in a proportion of 0.4 mg/ml to adjust the pH of the medium to 6.5. [Pg.646]

Potassium nitrate powder tends to cake gradually. But recently we can have very fine powder made by a method using a surface activator, which prevents the powder grains from caking. In this form it is handly to use, but when we use it in solution or when it is consolidated in a composition by pressure only without a binding agent e.g. blackpowder for rocket propellants, it is better to use the former. [Pg.86]

Potassium chlorate powder made by crushing the crystals, tend to cake more than pdtassium nitrate. But now we have a very fine powder which is made by using a surface activator as with potassium nitrate. This does not cake and is very useful, but in the match and other industries which use the chlorate in solution, the former is much preferred. [Pg.88]

Addition of surface active agents, such as triphenylmcthanc dyestuffs, can prevent caking of ammonium nitrate in quantity as low as 0.05% (see Vol. 11. p. 454) and [19). [Pg.582]

Fig. 2-11. Concentration distribution of metals along a vertical tube during introduction of air bubbles into the bottom of a tube (A) copper (B) manganese. Experiments 1 - without surface active agents (SAA) 2- with SAA of 1% solution of acetic acid 3- with SAA of 1% solution of acetic acid and sodium nitrate (reproduced with permission from Putikov and Dukhanin, 1994). Fig. 2-11. Concentration distribution of metals along a vertical tube during introduction of air bubbles into the bottom of a tube (A) copper (B) manganese. Experiments 1 - without surface active agents (SAA) 2- with SAA of 1% solution of acetic acid 3- with SAA of 1% solution of acetic acid and sodium nitrate (reproduced with permission from Putikov and Dukhanin, 1994).
Dispersion in liquid/liquid L/L) systems is associated with the enlargement of the interface area between two immiscible liquids, so that e.g. an extraction process or a chemical reaction (saponification, nitration, etc.) can proceed rapidly or dispersions of particular droplet size are produced (bead and suspension polymerizations, etc.). In this chapter only dispersion by stirrers is considered. If this process is assisted by the addition of surface-active substances, it is termed emulsification, for which completely different laws generally apply, see e.g. [201]. [Pg.244]


See other pages where Surface activation nitrate is mentioned: [Pg.506]    [Pg.228]    [Pg.280]    [Pg.433]    [Pg.255]    [Pg.18]    [Pg.253]    [Pg.228]    [Pg.436]    [Pg.165]    [Pg.338]    [Pg.278]    [Pg.94]    [Pg.1760]    [Pg.253]    [Pg.1602]    [Pg.34]    [Pg.190]    [Pg.363]    [Pg.381]    [Pg.387]    [Pg.201]    [Pg.582]    [Pg.326]    [Pg.122]    [Pg.190]    [Pg.398]    [Pg.18]    [Pg.41]   


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Nitrate activity

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