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Calcium dispersion

For comparison with Tables I and II, Table lit gives the range and typical values of the mineral distributions observed in bituminous coals by the CCSEM and Mossbauer techniques, derived from studies of perhaps a hundred different bituminous coal samples in this laboratory. Some obvious differences in mineralogy are apparent. In addition to the difference in calcium dispersion and abundance already noted, it is seen that certain minerals common in bituminous coals, such as Fe-bearing clays (illite and chlorite) and siderite, are virtually absent in the low-rank samples of Tables I and II. Conversely, minerals such as barite (BaSO ), apatite (Ca5(P0 )30H), and other Ca, Sr phosphates are rather uncommon in bituminous coals. [Pg.166]

Pure calcium monophosphide, CaP, is best prepared by passing phosphine into calcium dispersed in liquid ammonia. The addition compound which is formed can then be heated at 150°C to give the monophosphide, which above 600°C converts into a lower phosphide with loss of phosphorus (8.16). The lower phosphide liberates phosphine on contact with water (8.17). It is made commercially by heating quicklime in phosphorus vapour, and, together with Mg3P2, it finds application in sea flares. Sea flares are spontaneously inflammable due to the presence of small quantities of diphosphine which arise from the presence of impurity CaP (8.15). [Pg.601]

Uses High calcium dispersion power cobuilder in phosphate-free washing powds. [Pg.1748]

Two nucleation processes important to many people (including some surface scientists ) occur in the formation of gallstones in human bile and kidney stones in urine. Cholesterol crystallization in bile causes the formation of gallstones. Cryotransmission microscopy (Chapter VIII) studies of human bile reveal vesicles, micelles, and potential early crystallites indicating that the cholesterol crystallization in bile is not cooperative and the true nucleation time may be much shorter than that found by standard clinical analysis by light microscopy [75]. Kidney stones often form from crystals of calcium oxalates in urine. Inhibitors can prevent nucleation and influence the solid phase and intercrystallite interactions [76, 77]. Citrate, for example, is an important physiological inhibitor to the formation of calcium renal stones. Electrokinetic studies (see Section V-6) have shown the effect of various inhibitors on the surface potential and colloidal stability of micrometer-sized dispersions of calcium oxalate crystals formed in synthetic urine [78, 79]. [Pg.338]

The dispersing elemenf is usually a diffraction grating or an inferferomefer wifh a beamsplitter made from silicon-coafed or germanium-coafed quartz or calcium fluoride. [Pg.62]

Docusate calcium is used both as a fecal softening agent and an emulsifier, ie, a wetting or dispersing agent for external preparations (see Emulsions). [Pg.201]

Gum ghatti is the calcium and magnesium salt of a complex polysaccharide which contains L-arabinose, D-galactose, D-mannose, and D-xylose and D-glucuronic acid (48) and has a molecular weight of approximately 12,000. On dispersion in water, gum ghatti forms viscous solutions of viscosity intermediate between those of gum arabic and gum karaya. These dispersions have emulsification and adhesive properties equivalent to or superior to those described for gum arabic. [Pg.434]

Available Forms. Phthalocyanines are available as powders, in paste, or Hquid forms. They can be dispersed in various media suitable for aqueous, nonaqueous, or multipurpose systems, eg, polyethylene, polyamide, or nitrocellulose. Inert materials like clay, barium sulfate, calcium carbonates, or aluminum hydrate are the most common soHd extenders. Predispersed concentrates of the pigments, like flushes, are interesting for manufacturers of paints and inks (156), who do not own grinding or dispersing equipment. Pigment—water pastes, ie, presscakes, containing 50—75% weight of water, are also available. [Pg.506]

Pre-liming. Lime slurry, 0.25% lime on juice (0.250 g of CaO/100 g juice), is added to bring the pH of the mixture into the alkaline range. Insoluble calcium salts are precipitated as finely dispersed coUoids. Calcium carbonate in the form of recycled first carbonation sludge is added to provide coUoid absorption and stabilization. Temperature may be cool (50°C) or hot (80°C) depending on the temperature of the next step, or occasionally on the type of diffusion equipment. Retention time is 15 to 30 min. [Pg.26]

In the presence of a potassium catalyst dispersed on calcium oxide, toluene reacts with 1,3-butadiene to yield 5-phenyl-2-pentane (22). [Pg.176]

The most commonly used scale inhibitors are low molecular weight acrylate polymers and organophosphoms compounds (phosphonates). Both classes of materials function as threshold inhibitors however, the polymeric materials are more effective dispersants. Selection of a scale control agent depends on the precipitating species and its degree of supersaturation. The most effective scale control programs use both a precipitation inhibitor and a dispersant. In some cases this can be achieved with a single component (eg, polymers used to inhibit calcium phosphate at near neutral pH). [Pg.271]

Ghelants and Precipitation Inhibitors vs Dispersants. Dispersants can inhibit crystal growth, but chelants, such as ethylenediaminetetraacetic acid [60-00-4] (EDTA), and pure precipitation inhibitors such as nitrilotris(methylene)tris-phosphonic acid [6419-19-8], commonly known as amino trismethylene phosphonic acid (ATMP), can be more effective under certain circumstances. Chelants can prevent scale by forming stoichiometric ring stmctures with polyvalent cations (such as calcium) to prevent interaction with anions (such as carbonate). Chelants interact... [Pg.149]

Calcium carbonate is controlled with poly(maleic acid) (26) and organic phosphonates. Dispersants designed to control silica and magnesium silicate (7,27,28) have been introduced. [Pg.151]

Seawater Distillation. The principal thermal processes used to recover drinking water from seawater include multistage flash distillation, multi-effect distillation, and vapor compression distillation. In these processes, seawater is heated, and the relatively pure distillate is collected. Scale deposits, usually calcium carbonate, magnesium hydroxide, or calcium sulfate, lessen efficiency of these units. Dispersants such as poly(maleic acid) (39,40) inhibit scale formation, or at least modify it to form an easily removed powder, thus maintaining cleaner, more efficient heat-transfer surfaces. [Pg.151]


See other pages where Calcium dispersion is mentioned: [Pg.153]    [Pg.153]    [Pg.294]    [Pg.413]    [Pg.253]    [Pg.143]    [Pg.234]    [Pg.23]    [Pg.99]    [Pg.102]    [Pg.175]    [Pg.178]    [Pg.178]    [Pg.178]    [Pg.228]    [Pg.312]    [Pg.313]    [Pg.12]    [Pg.499]    [Pg.55]    [Pg.81]    [Pg.83]    [Pg.101]    [Pg.103]    [Pg.305]    [Pg.306]    [Pg.200]    [Pg.231]    [Pg.263]    [Pg.461]    [Pg.411]    [Pg.466]    [Pg.530]    [Pg.150]    [Pg.151]    [Pg.151]    [Pg.151]   
See also in sourсe #XX -- [ Pg.153 ]




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