Precipitated particle sizes Particles

In the polymer industry, post-reaction product treatment processes such as liquid-solid separation, drying, precipitation, particle size control, and polymer purification are very complex and costly. Future polymer plants should be designed such that process equipment can be easily and quickly converted to making new products at minimal cost and with... 

Eniistiin and Turkevichf prepared SrS04 (p = 3.96 g cm-3) precipitates under conditions that resulted in different particle sizes. Particle sizes were characterized by electron microscopy, and solubilities were determined at 25°C by a radiotracer technique. In the following data the supersaturation ratios are presented for different preparations, each of which is characterized by an average particle width and a minimum particle width ... 

The cadmium red pigment intermediate is obtained as a precipitate which is filtered off, washed, and calcined at approx. 600 °C. As with cadmium yellow, calcination yields the red pigment and determines the particle size, particle size distribution, and color shade. Analogously to the cadmium yellow process, cadmium red can be produced by direct reaction of cadmium oxide or cadmium carbonate with sulfur and the required amount of selenium at approx. 600 °C. 

Crystal packing of a precipitate (particle size) also influences the color of a precipitate. For example, large crystals of solid NaFeEDTA are dark brown in color, while powder precipitate is yellow. Do not be fooled by comparing the color of your product with a lab-mate s color ... 

In geometrically similar systems there is complete similarity if all necessary dimensionless criteria derived either from differential equations or by using the pi theorem are equal. In complex precipitation processes such complete similarity is impossible. Moreover, because we want to obtain identical not similar products from the systems differing in scale, we usually want to reproduce the product quality (particle size, particle morphology), mixture composition, and structure of the suspension on a larger scale. We thus use limited similarity, which means that we lose several degrees of freedom (we cannot manipulate particle size, solution composition, viscosity, and diffu-sivity), and we obtain this way a reduced number of similarity criteria. 

Key words Manganites/SOFC Cathode Materials/Synthesis/Co-Precipitation/Particle Size... 

Digestion is the process of allowing a precipitate to stand in contact with the mother liquor for some period of time, usually with heating. Digestion promotes slow recrystallization of the precipitate. Particle size increases and impurities tend to be expelled from the crystal. 

The precipitate particle size and morphology were determined using a Jeol JSM 8404 SEM. Chemical composition was analysed using a Biochrom Libras 70PC UV/Visible Spectrophotometer, Varian SpectrAA 55B Flame AAS and Setaram SetSys-Evo 1600 Thermal analyser together with a Pfeiffer OmniStar Quadrupole MS. The relative error of the standard chemical analyses (P, Ca, Mg, Zn, Sr and Na) was less than 5%. Specific surface area (SSA) was determined with Costech instruments Sorbtometer KELVIN 1042. 

If a dilute acid is added to this solution, a white gelatinous precipitate of the hydrated tin(IV) oxide is obtained. It was once thought that this was an acid and several formulae were suggested. However, it now seems likely that all these are different forms of the hydrated oxide, the differences arising from differences in particle size and degree of hydration. When some varieties of the hydrated tin(IV) oxide dissolve in hydrochloric acid, this is really a breaking up of the particles to form a colloidal solution—a phenomenon known as peptisation. 

Precipitate particles grow in size because of the electrostatic attraction between charged ions on the surface of the precipitate and oppositely charged ions in solution. Ions common to the precipitate are chemically adsorbed, extending the crystal lattice. Other ions may be physically adsorbed and, unless displaced, are incorporated into the crystal lattice as a coprecipitated impurity. Physically adsorbed ions are less strongly attracted to the surface and can be displaced by chemically adsorbed ions. 

By carefully controlling the precipitation reaction we can significantly increase a precipitate s average particle size. Precipitation consists of two distinct events nu-cleation, or the initial formation of smaller stable particles of precipitate, and the subsequent growth of these particles. Larger particles form when the rate of particle growth exceeds the rate of nucleation. 

An additional method for increasing particle size deserves mention. When a precipitate s particles are electrically neutral, they tend to coagulate into larger particles. Surface adsorption of excess lattice ions, however, provides the precipitate s particles with a net positive or negative surface charge. Electrostatic repulsion between the particles prevents them from coagulating into larger particles. 

The enthalpy of the copolymerization of trioxane is such that bulk polymerization is feasible. For production, molten trioxane, initiator, and comonomer are fed to the reactor a chain-transfer agent is in eluded if desired. Polymerization proceeds in bulk with precipitation of polymer and the reactor must supply enough shearing to continually break up the polymer bed, reduce particle size, and provide good heat transfer. The mixing requirements for the bulk polymerization of trioxane have been reviewed (22). Raw copolymer is obtained as fine emmb or flake containing imbibed formaldehyde and trioxane which are substantially removed in subsequent treatments which may be combined with removal of unstable end groups. 

When initiator is first added the reaction medium remains clear while particles 10 to 20 nm in diameter are formed. As the reaction proceeds the particle size increases, giving the reaction medium a white milky appearance. When a thermal initiator, such as AIBN or benzoyl peroxide, is used the reaction is autocatalytic. This contrasts sharply with normal homogeneous polymerizations in which the rate of polymerization decreases monotonicaHy with time. Studies show that three propagation reactions occur simultaneously to account for the anomalous auto acceleration (17). These are chain growth in the continuous monomer phase chain growth of radicals that have precipitated from solution onto the particle surface and chain growth of radicals within the polymer particles (13,18). 

Formation of a gelatinous precipitate that is difficult to filter can be avoided by addition of magnesium oxide to the acid solution. In order to increase particle size it is often necessary to keep the solution hot for several hours however, this problem is avoided by heating an intimate mixture of ammonium bifluoride with magnesium carbonate to 150—400°C (11). Particles of Mgp2 similar in size to those of the magnesium carbonate are obtained. 

Aluminum hydroxide gel may be prepared by a number of methods. The products vary widely in viscosity, particle size, and rate of solution. Such factors as degree of supersaturation, pH during precipitation, temperature, and nature and concentration of by-products present affect the physical properties of the gel. 

Precipitation Hardening. With the exception of ferritic steels, which can be hardened either by the martensitic transformation or by eutectoid decomposition, most heat-treatable alloys are of the precipitation-hardening type. During heat treatment of these alloys, a controlled dispersion of submicroscopic particles is formed in the microstmeture. The final properties depend on the manner in which particles are dispersed, and on particle size and stabiUty. Because precipitation-hardening alloys can retain strength at temperatures above those at which martensitic steels become unstable, these alloys become an important, in fact pre-eminent, class of high temperature materials. 

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