SUBJECTS dissolution

Sa.tura.tion Index. Materials of constmction used in pools are subject to the corrosive effects of water, eg, iron and copper equipment can corrode whereas concrete and plaster can undergo dissolution, ie, etching. The corrosion rate of metallic surfaces has been shown to be a function of the concentrations of Cl ,, dissolved O2, alkalinity, and Ca hardness as well as buffer intensity, time, and the calcium carbonate saturation index (35). 

Trifluoromethylpteridine and its 7-methyl and 6,7-dimethyl derivatives (69JCS(C)l75l) are, as expected, even more subject to hydration. The first two are essentially completely hydrated across the 3,4-double bond at equilibrium in neutral solution and the last is partly hydrated. On dissolution of 4-trifluoromethylpteridine in aqueous acid the 5,6,7,8-dihy-drated cation is the main product initially, rearranging more slowly to the thermodynamically more stable 3,4-hydrate. 

Another factor in this reaction sequence is also subject to external modification, namely, moderation of the basic oceanic dissolution of CO2 through temperature dependence of its solubility, S. The latter is defined as ... 

As further confirmation of this Rozenfeld has reviewed Russian work on this subject and reports that in pickling with sulphuric acid the amount of acid used in scale dissolution is only about one-tenth that consumed by the dissolution (corrosion) of the underlying metal. However, in hydrochloric acid the direct scale dissolution occurs to a much greater degree, and is responsible for about 40% of the acid consumption. 

Dissolution of Human Urinary Calculi in Vitro. Five human urinary calculi containing various proportions of Ca3(P04)2, Ca(C204), CaC03, and MgNH4(P04) were subjected to similar dissolution tests at pH 7 (Table 11). The same dissolution patterns as those of the model phosphate and oxalate calculi are found. That is, for phosphate calculi no. 1-4, X is more effective than [18]aneN6 or EDTA and for oxalate calculus no. 5, EDTA is best. 

Buildings, Monuments and Materials. Many materials used in man-made structures are subject to deterioration from normal weathering such as dissolution, mechanical fracture, erosion, and photochemical reactions. However, as shown by Amoroso and Fassina (43 the rates of deterioration have increased drastically since the advent of industrial pollution. Losses to Canadian heritage sites such as the federal parliament buildings has been significant and have been described by Weaver (44). 

While the solubility constants for various potential solids can indicate which solid is thermodynamically stable under a given set of conditions, reactions involving precipitation or dissolution of a solid are typically more subject to kinetic limitations than are reactions that take... 

Nanoparticles of the semicondnctor titanium dioxide have also been spread as mono-layers [164]. Nanoparticles of TiOi were formed by the arrested hydrolysis of titanium iso-propoxide. A very small amount of water was mixed with a chloroform/isopropanol solution of titanium isopropoxide with the surfactant hexadecyltrimethylammonium bromide (CTAB) and a catalyst. The particles produced were 1.8-2.2 nm in diameter. The stabilized particles were spread as monolayers. Successive cycles of II-A isotherms exhibited smaller areas for the initial pressnre rise, attributed to dissolution of excess surfactant into the subphase. And BAM observation showed the solid state of the films at 50 mN m was featureless and bright collapse then appeared as a series of stripes across the image. The area per particle determined from the isotherms decreased when sols were subjected to a heat treatment prior to spreading. This effect was believed to arise from a modification to the particle surface that made surfactant adsorption less favorable. 

More recently copper phosphate cements have been suggested for use as controlled-release agents for supplying trace amounts of copper to cattle and sheep over an extended period (Allen et al., 1984 Mansion et al., 1985 Prosser et al., 1986). The cements were prepared with a Cu/P ratio of 1 1 to ensure that the matrix was an add phosphate and so subject to dissolution in aqueous solutions. They released copper at a constant rate for 90 days. 

In trace organic analysis there is usually an extraction or clean-up process, rather than a sample dissolution. Here not only must the matrix effect be considered, but also the recovery yield of the extraction. Frequently an external spike standard is added, but there is often no way of knowing if the recovery of the spike standard matches the analyte in question. There is considerable evidence that the U S E P A method for VOA analysis (Minnich 1993) is subject to such error, as reported by Schumacher and Ward (7997). The analyst must always consider the possibility of such an error, especially when using CRMs to control methods that are applied in routine mode. 

The principal member of the first class is tributyl phosphate (TBP). It is convenient to use this organic reagent in the refining of yellow cake consequent to nitric acid dissolution. After dilution, the solution is subjected to filtration through vacuum filters prior to intro-... 

By their nature, many UV absorbers are amenable to analysis by fluorimetric analysis. In many instances visible fluorescence techniques are less subject to interference by other polymer additives in a polymer extract than are UV methods of analysis. In fluorescence analysis (ex at 367 nm, em at 400-440 nm) of a PS/Uvitex OB chloroform dissolution AOs such as Ionol CP, Ionox 330, Polygard and Wingstay T/W do not interfere detection limit of 10 ppm [41]. 

Decomposition and dissolution processes are generally subject to fairly large sources of error, namely ... 

Different analytical procedures have been developed for direct atomic spectrometry of solids applicable to inorganic and organic materials in the form of powders, granulate, fibres, foils or sheets. For sample introduction without prior dissolution, a sample can also be suspended in a suitable solvent. Slurry techniques have not been used in relation to polymer/additive analysis. The required amount of sample taken for analysis typically ranges from 0.1 to 10 mg for analyte concentrations in the ppm and ppb range. In direct solid sampling method development, the mass of sample to be used is determined by the sensitivity of the available analytical lines. Physical methods are direct and relative instrumental methods, subjected to matrix-dependent physical and nonspectral interferences. Standard reference samples may be used to compensate for systematic errors. The minimum difficulties cause INAA, SNMS, XRF (for thin samples), TXRF and PIXE. 

Quantitative analysis of multicomponent additive packages in polymers is difficult subject matter, as evidenced by results of round-robins [110,118,119]. Sample inhomogeneity is often greater than the error in analysis. In procedures entailing extraction/chromatography, the main uncertainty lies in the extraction stage. Chromatographic methods have become a ubiquitous part of quantitative chemical analysis. Dissolution procedures (without precipitation) lead to the most reliable quantitative results, provided that total dissolution can be achieved follow-up SEC-GC is molecular mass-limited by the requirements of GC. Of the various solid-state procedures (Table 10.27), only TG, SHS, and eventually Py, lead to easily obtainable accurate quantitation. 

Table 10.32 is a shortlist of the characteristics of the ideal polymer/additive analysis technique. It is hoped that the ideal method of the future will be a reliable, cost-effective, qualitative and quantitative, in-polymer additive analysis technique. It may be useful to briefly compare the two general approaches to additive analysis, namely conventional and in-polymer methods. The classical methods range from inexpensive to expensive in terms of equipment they are well established and subject to continuous evolution and their strengths and deficiencies are well documented. We stressed the hyphenated methods for qualitative analysis and the dissolution methods for quantitative analysis. Lattimer and Harris [130] concluded in 1989 that there was no clear advantage for direct analysis (of rubbers) over extract analysis. Despite many instrumental advances in the last decade, this conclusion still largely holds true today. Direct analysis is experimentally somewhat faster and easier, but tends to require greater interpretative difficulties. Direct analysis avoids such common extraction difficulties as ... 

Diarrheal conditions may decrease drug absorption as a result of reduced intestinal residence time. The absorption of several drugs was decreased in response to lactose- and saline-induced diarrhea [145]. Digoxin absorption from tablets was impaired in one subject who developed chronic diarrhea as a result of x-ray treatment [146]. Abdominal radiation or the underlying disease has been shown to reduce digoxin and clorazepate absorption [147]. A dosage form that provides rapid drug dissolution (e.g., solution) may partially resolve this problem. 

This topic is the subject of Chapter 15, but some of the materials that are used in these systems have other uses as well (Table 5). Materials used to modify dissolution can be incorporated in the formulation on either a dry or wet basis. Table 11 lists some of the more commonly used controlled release excipients. 

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