Precipitate formation hardness ions

Sequestration forms the basis for detergent and water-treatment appHcations of polyphosphates. Sequestration of hardness ions by sodium tripolyphosphate used in detergent formulations prevents the precipitation of surfactants by the hardness ions. Sodium polyphosphate glass (SHMP) may be added to water system to prevent the formation of calcium or magnesium scales by reducing the activity of the hardness ions. However, if the ratio of cation to polyphosphate is too high at a given pH, insoluble precipitates such as may result instead of the soluble polyphosphate complexes. The... 

The corrosion process can be inhibited by the addition of phosphate or polyphosphate ions [344], inorganic inhibitors as, for example, chromate ions [336], adsorbed alcohols [345], adsorbed amines, competing with anions for adsorption sites [339,] as well as saturated linear aliphatic mono-carboxylate anions, CH3(CH2)n-2COO , n = 7 — 11, [24]. In the latter case, the formation of the passive layer requires Pb oxidation to Pb + by dissolved oxygen and then precipitation of hardly soluble lead carboxylate on the metal surface. The corrosion protection can also be related to the hydrophobic character of carboxylate anions, which reduce the wetting of the metal surface. 

SDS has several advantages over soap. Unlike the carboxylate anions in soap, the dodecylsulfate anion does not form insoluble precipitates with hard water ions (e.g., Ca2+), leading to the formation of soap scum. Also, the dodecylsulfate anion is the conjugate base of a very strong acid (H2S04). Therefore, SDS is a weak base, and solutions of SDS are pH neutral. 

Several alkaline chemicals have been employed for various aspects of enhanced oil recovery. Two of the most favorable alkaline chemicals tested and used in tertiary oil recovery are sodium orthosilicate and sodium hydroxide. Comparing their characteristics, both chemicals react with acids in crude oil to form surfactants, precipitate hardness ions and change rock surface wettability. One difference between the two chemicals is that the interfacial properties for sodium orthosilicate systems are less affected by hardness ions (13), hence slightly lower interfacial tensions would occur. Lower Interfacial tensions can aid in in-situ emulsion formation. 

Four water samples from the surrounding area of the East Bodo Reservoir were analyzed for ion composition (see Table 2). The total dissolved solid content ranged from 25,000 to 29,000 ppm, with hardness ion concentrations (Ca++ and Mg++) ranging fi-om 350 ppm to 650 ppm. Hardness ions significantly reduce the effectiveness of the polymer viscosity and, in sufficient concentrations, may lead to precipitation of the polymer. The formation of carbonate scales with hardness ions may also be a factor. Thus,... 

Hydroxides. The hydrolysis of uranium has been recendy reviewed (154,165,166), yet as noted in these compilations, studies are ongoing to continue identifying all of the numerous solution species and soHd phases. The very hard uranium(IV) ion hydrolyzes even in fairly strong acid (- 0.1 Af) and the hydrolysis is compHcated by the precipitation of insoluble hydroxides or oxides. There is reasonably good experimental evidence for the formation of the initial hydrolysis product, U(OH) " however, there is no direct evidence for other hydrolysis products such as U(OH) " 2> U(OH)" 2> U(OH)4 (or UO2 2H20). There are substantial amounts of data, particulady from solubiUty experiments, which are consistent with the neutral species U(OH)4 (154,167). It is unknown whether this species is monomeric or polymeric. A new study under reducing conditions in NaCl solution confirms its importance and reports that it is monomeric (168). 8olubihty studies indicate that the anionic species U(OH) , if it exists, is only of minor importance (169). There is limited evidence for polymeric species such as Ug(OH) " 25 (1 4). 

The presence of a sufficientiy strong chelating agent, ie, one where K in equation 26 is large, keeps the concentration of free metal ion suppressed so that pM is larger than the saturation pM given by the solubiUty product relation (eq. 29) and no soHd phase of MX can form even in the presence of relatively high anion concentrations. The metal is thus sequestered with respect to precipitation by the anion, such as in the prevention of the formation of insoluble soaps in hard water. 

The effectiveness with which divalent ions cause gelation of poly(acrylic add) has been found to follow the order Ba > Sr > Ca (Wall Drenan, 1951) and this has been attributed to the formation of salt-like crosslinks. Gelation has been assumed to arise in part from dehydration of the ion-pairs (Ikegami Imai, 1962), and certainly correlates with predpitation in fairly dilute systems. Indeed, the term precipitation has sometimes been applied to the setting of AB cements derived from poly(acrylic add) as they undergo the transition from soft manipulable paste to hard brittle solid. 

Several operations may be employed to treat water prior to use. Aeration is used to drive off odorous gases, such as H2S, and to oxidize soluble Fe2+ and Mn2+ ions to insoluble forms. Lime is added to remove dissolved calcium (water hardness). A12(S04)3 forms a sticky precipitate of Al(OH)3, which causes very tine particles to settle. Various filtration and settling processes are employed to treat water. Chlorine, Cl2, is added to kill bacteria. Formation of undesirable byproducts of water chlorination may be avoided by disinfection with chlorine dioxide, C102, or ozone, 03. 

Under real circumstances equilibrium conditions are difficult to attain, and kinetic criteria (which are often hard to predict) play a key role. To complicate matters, the stoichiometries of some of these reactions do not obey their theoretical chemical equations. In addition, the formation of a solid phase can be the result of successive reactions with varied rates. See, for example, the simplified precipitation pathway of ferric ions with hydroxide ions, depicted in Figure 5.7. 

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