Water with anions

In order to saturate water with anions A and B , different concentrations of cation M are needed ... 

Methyl green, purified to remove crystal violet impurity, can be used as a reagent to determine trace contamination of water with anionic surfactant. If a 200-mL sample, acidified and containing methyl green, is extracted with 5 mL chloroform, any green color in the extract signifies the presence of anionic surfactant (31). 

Saito, T., K. Hagiwara, Surfactants in water with anion-exchange resin and polymeric adsorbent, Fresenius Z. Anal. Chem., 1982,312, 533-535. 

Deamidation of soy and other seed meal proteins by hydrolysis of the amide bond, and minimization of the hydrolysis of peptide bonds, improves functional properties of these products. For example, treatment of soy protein with dilute (0.05 A/) HCl, with or without a cation-exchange resin (Dowex 50) as a catalyst (133), with anions such as bicarbonate, phosphate, or chloride at pH 8.0 (134), or with peptide glutaminase at pH 7.0 (135), improved solubiHty, whipabiHty, water binding, and emulsifying properties. 

Flocculation. The interaction of the cationic PEIs with anionic substrates leads to substrate flocculation. AppHcations of this property include the coagulation of latex (434), commercial appHcation in effluent treatments (435—437), and stabiHzation of highly loaded coal—water mixtures in mining (438). 

Quats are usually moderately soluble ia water, but this varies widely owiag to the range of groups bonded to the nitrogen. They are fundamentally nonreactive but act as surface—active cations. Compatibility with anionic detergents and activity ia the presence of hard water have been claimed for some quats (19). 

Stannous Sulfate. Stannous sulfate (tin(Il) sulfate), mol wt 214.75, SnSO, is a white crystalline powder which decomposes above 360°C. Because of internal redox reactions and a residue of acid moisture, the commercial product tends to discolor and degrade at ca 60°C. It is soluble in concentrated sulfuric acid and in water (330 g/L at 25°C). The solubihty in sulfuric acid solutions decreases as the concentration of free sulfuric acid increases. Stannous sulfate can be prepared from the reaction of excess sulfuric acid (specific gravity 1.53) and granulated tin for several days at 100°C until the reaction has ceased. Stannous sulfate is extracted with water and the aqueous solution evaporates in vacuo. Methanol is used to remove excess acid. It is also prepared by reaction of stannous oxide and sulfuric acid and by the direct electrolysis of high grade tin metal in sulfuric acid solutions of moderate strength in cells with anion-exchange membranes (36). 

Acid Dyes. These water-soluble anionic dyes ate appHed to nylon, wool, sUk, and modified acryHcs. They ate also used to some extent for paper, leather, food, and cosmetics. The original members of this class aU had one or mote sulfonic or catboxyHc acid groups in thein molecules. This characteristic probably gave the class its name. Chemically, the acid dyes consist of azo (including preformed metal complexes), anthraquiaone, and ttiaryHnethane compounds with a few azHie, xanthene, ketone imine, nitro, nitroso, and quHiophthalone compounds. 

In sea water with a pH of 8, crevice pH may fall helow 1 and chloride concentration can be many times greater than in the water. The crevice environment becomes more and more corrosive with time as acidic anions concentrate within. Areas immediately adjacent to the crevice receive ever-increasing numbers of electrons from the crevice. Hydroxyl ion formation increases just outside the crevice—locally increasing pH and decreasing attack there (Reaction 2.2). Corrosion inside the crevice becomes more severe with time due to the spontaneous concentration of acidic anion. Accelerating corrosion is referred... 

Tubercles are mounds of corrosion product and deposit that cap localized regions of metal loss. Tubercles can choke pipes, leading to diminished flow and increased pumping costs (Fig. 3.1). Tubercles form on steel and cast iron when surfaces are exposed to oxygenated waters. Soft waters with high bicarbonate alkalinity stimulate tubercle formation, as do high concentrations of sulfate, chloride, and other aggressive anions. 

Like strong acid resins, strong base resins are highly ionized and can be used over the entire pH range. These resins are used in the hydroxide (OH) form for water deionization. They will react with anions in solution and can convert an acid solution to pure water ... 

Sn2 reactions with anionic nucleophiles fall into this class, and observations are generally in accord with the qualitative prediction. Unusual effects may be seen in solvents of low dielectric constant where ion pairing is extensive, and we have already commented on the enhanced nucleophilic reactivity of anionic nucleophiles in dipolar aprotic solvents owing to their relative desolvation in these solvents. Another important class of ion-molecule reaction is the hydroxide-catalyzed hydrolysis of neutral esters and amides. Because these reactions are carried out in hydroxy lie solvents, the general medium effect is confounded with the acid-base equilibria of the mixed solvent lyate species. (This same problem occurs with Sn2 reactions in hydroxylic solvents.) This equilibrium is established in alcohol-water mixtures ... 

In the pulp and paper industry, anionic and cationic acrylamide polymers are used as chemical additives or processing aids. The positive effect is achieved due to a fuller retention of the filler (basically kaoline) in the paper pulp, so that the structure of the paper sheet surface layer improves. Copolymers of acrylamide with vi-nylamine not only attach better qualities to the surface layer of.paper, they also add to the tensile properties of paper in the wet state. Paper reinforcement with anionic polymers is due to the formation of complexes between the polymer additive and ions of Cr and Cu incorporated in the paper pulp. The direct effect of acrylamide polymers on strength increases and improved surface properties of paper sheets is accompanied by a fuller extraction of metallic ions (iron and cobalt, in addition to those mentioned above), which improves effluent water quality. 

In the pyroaurite structure the brucite layers are cationic. However, on oxidation the resultant brucite layers in y - NiOOH are anionic. To preserve electroneutrality, cations and anions are exchanged in the intercalated layer during the oxidation-reduction process. This is illustrated in Fig. 4. In the case of Mn-substituted materials, some Mn can be reduced to Mn(II). This neutralizes the charge in the brucite layer this part of the structure reverts to the P - Ni(OH)2 structure and the intercalated water and anions are expelled from the lattice. With this there is a concomitant irreversible contraction of the interlayer spacing from 7.80 to 4.65A [72]. 

Lack of dealkalization with high alkalinity MU water NOTE Anion dealkalizers do not use acid, but also do not reduce MU water TDS and introduce additional chlorides (risk of pitting). Excessive CR line corrosion BW carryover Low cycles of concentration higher operating costs... 

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