Ion content

In contrast to triaxial porcelains, packaging materials such as 99% AI2O2 prepared by a soHd-state sintering process, display significantly lower dielectric loss. In these materials, there is no residual glassy phase with its associated mobile ion content, and therefore, conduction losses are minimized. 

The waters through which ships travel are categorized by their salt content. The following are approximate values seawater, 3.0 to 4.0% salt coastal brackish water, 1.0 to 3.0% river brackish water, 0.5 to 1.8% salty river water, 0.05 to 0.5% river water, <0.05%. Seawater mainly contains NaCl. The salt content is approximately 1.8 times the chloride ion content. The salt content of the world s oceans is almost the same. Different salt contents can occur in more enclosed seas [e.g., the Adriatic (3.9%), Red Sea (4.1%) and the Baltic (1.0%)]. Table 17-1 gives as an example average analyses for seawater and the Rhine River. 

As the ion content of an ionomer increases, the proportion of the cluster phase to the multiplet-containing... 

Figure 1 (tan 5)max versus ion content for the multiplet phase and the cluster phase of Na-SPS ionomers. 

Figure 2 Modulus versus temperature for Na salts of PMMA ionomers of various ion contents.

As an indication of the changes in deformation modes that can be produced in ionomers by increase of ion content, consider poly(styrene-co-sodium methacrylate). In ionomers of low ion content, the only observed deformation mode in strained thin films cast from tetra hydrofuran (THF), a nonpolar solvent, is localized crazing. But for ion contents near to or above the critical value of about 6 mol%, both crazing and shear deformation bands have been observed. This is demonstrated in the transmission electron microscope (TEM) scan of Fig. 3 for an ionomer of 8.2 mol% ion content. Somewhat similar deformation patterns have also been observed in a Na-SPS ionomer having an ion content of 7.5 mol%. Clearly, in both of these ionomers, the presence of a... 

In general, as the ion content is raised, the modulus or stiffness of the ionomer is increased, as shown by the data in Fig. 2. While the increase is much greater in the elevated temperature range, where the polymer is acting more like a crosslinked rubber, there is still a significant increase in the glassy modulus below Tg. For example, for the PMMA-based ionomer of Fig. 2, the modulus at 30°C is almost 20% above that of the homopolymer for an ionomer having an ion content of 12.4 mol%. For the... 

In nonrigid ionomers, such as elastomers in which the Tg is situated below ambient temperature, even greater changes can be produced in tensile properties by increase of ion content. As one example, it has been found that in K-salts of a block copolymer, based on butyl acrylate and sulfonated polystyrene, both the tensile strength and the toughness show a dramatic increase as the ion content is raised to about 6 mol% [10]. Also, in Zn-salts of a butyl acrylate/acrylic acid polymer, the tensile strength as a function of the acrylic acid content was observed to rise from a low value of about 3 MPa for the acid copolymer to a maximum value of about 15 MPa for the ionomer having acrylic acid content of 5 wt% [II]. Other examples of the influence of ion content on mechanical properties of ionomers are cited in a recent review article [7],... 

Thermal treatment and the nature of the casting solvent can also affect the deformation modes achieved in strained films of ionomers. For example, in films cast from polar dimethylformamide (DMF), the solvent interacts with ion-rich clusters and essentially destroys them, as is evident form absence of a second, higher temperature loss peak in such samples. As a result, even in a cast DMF sample of Na-SPS ionomer of high ion content (8.5 mol%), the only deformation mode observed in tensile straining is crazing. However, when these films are given an additional heat treatment (41 h at 210°C), shear... 

As one example, in thin films of Na or K salts of PS-based ionomers cast from a nonpolar solvent, THF, shear deformation is only present when the ion content is near to or above the critical ion content of about 6 mol% and the TEM scan of Fig. 3, for a sample of 8.2 mol% demonstrates this but, for a THF-cast sample of a divalent Ca-salt of an SPS ionomer, having only an ion content of 4.1 mol%, both shear deformation zones and crazes are developed upon tensile straining in contrast to only crazing for the monovalent K-salt. This is evident from the TEM scans of Fig. 5. For the Ca-salt, one sees both an unfibrillated shear deformation zone, and, within this zone, a typical fibrillated craze. The Ca-salt also develops a much more extended rubbery plateau region than Na or K salts in storage modulus versus temperature curves and this is another indication that a stronger and more stable ionic network is present when divalent ions replace monovalent ones. Still another indication that the presence of divalent counterions can enhance mechanical properties comes from... 

Figure 5 TEM micrographs of deformed thin films of an SPS ionomer having an ion content of 4.1 mol% and cast from THF K salt (a), and Ca salt (b).

The combined effects of a divalent Ca counterion and thermal treatment can be seen from studies of PMMA-based ionomers [16]. In thin films of Ca-salts of this ionomer cast from methylene chloride, and having an ion content of only 0.8 mol%, the only observed deformation was a series of long, localized crazes, similar to those seen in the PMMA homopolymer. When the ionomer samples were subject to an additional heat treatment (8 h at 100°C), the induced crazes were shorter in length and shear deformation zones were present. This behavior implies that the heat treatment enhanced the formation of ionic aggregates and increased the entanglement strand density. The deformation pattern attained is rather similar to that of Na salts having an ion content of about 6 mol% hence, substitution of divalent Ca for monovalent Na permits comparable deformation modes, including some shear, to be obtained at much lower ion contents. 

The mechanical properties of ionomers are generally superior to those of the homopolymer or copolymer from which the ionomer has been synthesized. This is particularly so when the ion content is near to or above the critical value at which the ionic cluster phase becomes dominant over the multiplet-containing matrix phase. The greater strength and stability of such ionomers is a result of efficient ionic-type crosslinking and an enhanced entanglement strand density. 

Aside from ion content, a wide range of properties is available in ionomers by control of various processing variables, such as degree of conversion (neutralization), type of counterion, plasticizer content and thermal treatment. Various examples illustrating possible effects of these variables on mechanical relaxation behavior and on such mechanical properties as stiffness, strength, and time- or energy-to-fracture have been given. 

Determine the sulphate-ion content of an unknown solution, say ca 0.3 mg mL"1, using the calibration curve. 

Trace metals have to be removed, notably manganese, ferrous ions and zinc. This is often accomplished using the compound potassium hexacyanoferrate which predpitates or complexes the metals and, in excess, acts to inhibit growth and indirectly promotes dtric add production. The amount of potassium hexacyanoferrate required is variable depending on the nature of the ion content of the carbon source. 

Suggested maximum conductance values are intended to serve as an alarm for saltwater condenser leaks and can be correlelated with chloride ion content in FW and/or BW. 

Concept used in sophisticated scaling models, whereby certain ions in aqueous solution are said to associate in pairs (e.g., CaS04, CaHC03-). These ion pairs are then deducted from the total analytical value, to provide an estimate of the free ion content available for seed crystal scaling or growth agglomeration and deposition. 

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