Stabilization chemical

Figure 5.12 Relative chemical stability of carbonate minerals...

Chemical stability. The chemical stability of SA films is of interest in many areas. However, tliere is no general mle for it. The chemical stability of silane films is remarkable, due to tlieir intennolecular crosslinking. Therefore, tliey are found to be more stable tlian LB films. Alkyltrichlorosilane monolayers provide stmctures tliat are stable to chemical conditions tliat most LB films could not stand. However, photopolymerized LB films also show considerable stability in organic solvents. 

SAMs tliat are made out of stmctures capable of fonning strong intennolecular hydrogen bonds have been studied especially in view of tlieir expected high thennal and chemical stability [186, 187],... 

In tenns of an electrochemical treatment, passivation of a surface represents a significant deviation from ideal electrode behaviour. As mentioned above, for a metal immersed in an electrolyte, the conditions can be such as predicted by the Pourbaix diagram that fonnation of a second-phase film—usually an insoluble surface oxide film—is favoured compared with dissolution (solvation) of the oxidized anion. Depending on the quality of the oxide film, the fonnation of a surface layer can retard further dissolution and virtually stop it after some time. Such surface layers are called passive films. This type of film provides the comparably high chemical stability of many important constmction materials such as aluminium or stainless steels. 

Prepared feeds are marketed in various forms from very fine particles through cmmbles, flakes, and pellets. Pelleted rations may be hard, semimoist, or moist. Hard pellets typically contain less than 10% water and can be stored under cool, dry conditions for at least 90 days without deterioration of quahty. Semimoist pellets are chemically stabilized to protect them from degradation and mold if they are properly stored, while moist pellets must be frozen if they are not used immediately after manufacture. Moist feeds are produced in machines similar to sausage grinders. 

Chemical Stabilization. The chemistry of the system determines both the rate at which the polymer phase is formed and the rate at which it changes from a viscous fluid to a dimensionally stable cross-linked polymer phase. It also governs the rate at which the blowing agent is activated, whether it is due to temperature rise or to insolubilization in the Hquid phase. 

Chemical Stabilization Processes. This method is more versatile and thus has been used successfully for more materials than the physical stabilization process. Chemical stabilization is more adaptable for condensation polymers than for vinyl polymers because of the fast yet controUable curing reactions and the absence of atmospheric inhibition. 

Polyphenols. Another increa singly important example of the chemical stabilization process is the production of phenoHc foams (59—62) by cross-linking polyphenols (resoles and novolacs) (see Phenolic resins). The principal features of phenoHc foams are low flammabiUty, solvent resistance, and excellent dimensional stabiUty over a wide temperature range (59), so that they are good thermal iasulating materials. 

Other Materials. Foams from epoxy resias (59,60,85,86) and sihcone resias (32,60,87,88) can also be formed by a chemical stabilization... 

Chemical Stabilization Processes. Cellular mbber and ebonite are produced by chemical stabili2ation processes. 

Chemical stability of a-GdTbFe and a-TbFeCo is poor it is good for other materials. 

Dehydration or Chemical Stabilization. The removal of surface silanol (Si—OH) bonds from the pore network results in a chemically stable ultraporous soHd (step F, Fig. 1). Porous gel—siHca made in this manner by method 3 is optically transparent, having both interconnected porosity and sufficient strength to be used as unique optical components when impregnated with optically active polymers, such as fiuors, wavelength shifters, dyes, or nonlinear polymers (3,23). 

Stabilization. A critical step in preparing sol—gel products and especially Type VI siHca optical components is stabilization of the porous stmcture as indicated in Figure 1. Both thermal and chemical stabilization is required in order for the material to be used in an ambient environment. The reason for the stabilization treatment is the large concentration of hydroxyls on the surface of the pores of these high (>400 /g) surface area materials. 

Chemical stabilization involves removing the concentration of surface hydroxyls and surface defects, such as metastable three-membered rings, below a critical level so that the surface is not stressed by rehydroxylation in use. Thermal stabilization involves reducing the surface area sufficiently to enable the material to be used at a given temperature without reversible stmctural changes. The mechanisms of thermal and chemical stabilization are interrelated because of the extreme effects that surface hydroxyls and chemisorbed water have on stmctural changes. Full densification of gels, such as the... 

Raw juice is heated, treated sequentially with lime (CaO) and carbon dioxide, and filtered. This accomplishes three objectives (/) microbial activity is terminated (2) the thin juice produced is clear and only lightly colored and (J) the juice is chemically stabilized so that subsequent processing steps of evaporation and crystalliza tion do not result in uncontrolled hydrolysis of sucrose, scaling of heating surfaces, or coprecipitation of material other than sucrose. 

Thermal and Chemical Stability. In addition to load-bearing properties, tire reinforcement must be able to resist degradation by chemicals in cured mbber and heat generation. The most critical degradant depends on the material in use. Most thermoplastic reinforcements are either modified directiy or stabiH2ed with additives to offset some, mostiy thermal, degradation (32,33). 

Ceramic-matrix composites are a class of materials designed for stmctural applications at elevated temperature. The response of the composites to the environment is an extremely important issue. The desired temperature range of use for many of these composites is 0.6 to 0.8 of their processing temperature. Exposure at these temperatures will be for many thousands of hours. Therefore, the composite microstmcture must be stable to both temperature and environment. Relatively few studies have been conducted on the high temperature mechanical properties and thermal and chemical stability of ceramic composite materials. 

The high chemical stability of pterins towards aqueous base is due to anion formation suppressing nucleophilic attack at a ring carbon atom by electrostatic repulsion. Substitution... 

Chemical stability. The solvent should be chemically stable and, if possible, nonflammable. 

The immobilization of reagents onto sorbents often results in increase of their sensitivity and, in some cases, selectivity, allows to simplify the analysis and to avoid necessity of use of toxic organic solvents. At the same time silicas are characterized by absence of swelling, thenual and chemical stability, rapid achievement of heterogeneous equilibrium. 

Information pertaining to the hazards of the chemicals used in the process. This should contain at least the following information toxicity, flammability, permissible exposure limits, physical data, reactivity data, corrosivity data, thermal and chemical stability data, and hazardous effects of inadvertent mixing of different materials that could occur. 

The materials problems in the construction of microchips are related to both diffusion and chemical interactions between the component layers, as shown above. There is probably a link between drese two properties, since the formation of inter-metallic compounds of medium or high chemical stability frequently leads to tire formation of a compound ban ier in which tire diffusion coefficients of both components are lower than in the pure metals. 

Enamel coatings usually consist of several layers in which the prime coating is applied for adhesion but does not have the chemical stability of the outer layers. With cathodic polarization at holidays, attack on the exposed prime coating is possible as the cathodically produced alkali causes the defects to increase in size. This particularly cannot be excluded in salt-rich media. 

Enamels have very varied properties where their chemical stability is concerned. Relevant stability testing must be carried out for the different areas of application. Enamel coatings for hot water heaters, their requirements and combination with cathodic protection are described in Section 20.4.1. 

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