Calcium carbonate compounds

Generally it was found that 0.15 volume fraction small particles seem to be required to produce yield values. The yield value Y and viscosity level increase with both increasing particle loading (Figs. 5[a], [b]) and decreasing particle size (Fig. 5[c]). Note Y is largest for the ISAF compounds and lower for the FEE It is lowest for the SRF compounds. This is the same order as the particle size (ISAF has the smallest particles). Larger yield and viscosities are also found for calcium carbonate compounds [S25], For rubber compounds the yield value is of order 50 to 100 kPa and the power law exponent n about 0.2. In Table II, we present values Y,A,B,K, and n of Eqs. (56) and (57). 

Suetsugu [100] studied the tensile strength and the impact strength of polypropylene-calcium carbonate compounds and found it to be dominated by the dispersion of the agglomerate. He defined a dispersion index by... 

As described in Section 7.2, stearic acid is often added commercially to calcium carbonate compounds to break up agglomerates and reduce viscosity. It presumably increases tensile strength and impact strength. 

Chlorides of sodium, magnesium and calcium are almost always the prevailing compounds, along with gypsum and calcium carbonate. 

Place 45 g. (43 ml.) of benzal chloride (Section IV,22), 250 ml. of water and 75 g. of precipitated calcium carbonate (1) in a 500 ml. round-bottomed flask fltted with a reflux condenser, and heat the mixture for 4 hours in an oil bath maintained at 130°. It is advantageous to pass a current of carbon dioxide through the apparatus. Filter off the calcium salts, and distil the filtrate in steam (Fig. II, 40, 1) until no more oil passes over (2). Separate the benzaldehyde from the steam distillate by two extractions with small volumes of ether, distil off most of the ether on a water bath, and transfer the residual benzaldehyde to a wide-mouthed bottle or flask. Add excess of a concentrated solution of sodium bisulphite in portions with stirring or shaking stopper the vessel and shake vigorously until the odour of benzaldehyde can no longer be detected. Filter the paste of the benzaldehyde bisulphite compound at the pump... 

In addition to the main acidulation reaction, other reactions also occur. Free calcium carbonate in the rock reacts with the acid to produce additional by-product calcium compounds and CO2 gas which causes foaming. Other mineral impurities, eg, Fe, Al, Mg, U, and organic matter, dissolve, the result being that the wet-process acid is highly impure. 

Calcium. Calcium is the fifth most abundant element in the earth s cmst. There is no foreseeable lack of this resource as it is virtually unlimited. Primary sources of calcium are lime materials and gypsum, generally classified as soil amendments (see Calcium compounds). Among the more important calcium amendments are blast furnace slag, calcitic limestone, gypsum, hydrated lime, and precipitated lime. Fertilizers that carry calcium are calcium cyanamide, calcium nitrate, phosphate rock, and superphosphates. In addition, there are several organic carriers of calcium. Calcium is widely distributed in nature as calcium carbonate, chalk, marble, gypsum, fluorspar, phosphate rock, and other rocks and minerals. 

On archaeological glass objects, layers of reaction products are formed and the main constituents of these cmsts are the less-soluble compounds such as siHca and calcium carbonate, which becomes calcium sulfate. 

Precipitated Calcium Carbonate. Calcium carbonate [471-34-1] (Turns), CaCO, is a fine white microcrystaUine powder without odor or taste. It is stable in air. An aqueous suspension is close to neutrality. It is practically insoluble in water, insoluble in alcohol, and dissolves with effervescence in dilute acetic, hydrochloric, and nitric acids (see Calcium compounds, calcium carbonate). 

Alkali metal haHdes can be volatile at incineration temperatures. Rapid quenching of volatile salts results in the formation of a submicrometer aerosol which must be removed or else exhaust stack opacity is likely to exceed allowed limits. Sulfates have low volatiHty and should end up in the ash. Alkaline earths also form basic oxides. Calcium is the most common and sulfates are formed ahead of haHdes. Calcium carbonate is not stable at incineration temperatures (see Calcium compounds). Transition metals are more likely to form an oxide ash. Iron (qv), for example, forms ferric oxide in preference to haHdes, sulfates, or carbonates. SiHca and alumina form complexes with the basic oxides, eg, alkaH metals, alkaline earths, and some transition-metal oxidation states, in the ash. 

Fillers. These are used to reduce cost in flexible PVC compounds. It is also possible to improve specific properties such as insulation resistance, yellowing in sunlight, scuff resistance, and heat deformation with the use of fillers (qv). Typical filler types used in PVC are calcium carbonate, clays, siHca, titanium dioxide, and carbon black. 

In the calendering method, a PVC compound which contains plasticizers (qv) (60—120 phr), pigments (qv) (0—10 phr), fillers (qv) (20—60 phr), stabilizers (10—30 phr), and other additives, is kneaded with calender roUs at 150—200°C, followed by extmsion between clearance-adjusted roUs for bonding onto the substrate. This method is employed for products with thick PVC layers, ie, of 0.05—0.75 mm thickness. The main plasticizer used is di-2-ethylhexyl phthalate (DOP). For filler to reduce cost, calcium carbonate is mainly used. A woven or knit fabric made of cotton, rayon, nylon, polyester, and their blend fiber is used as substrate. For foamed vinyl-coated fabrics, the bonded materials are heated in an oven to decompose the foam-blowing... 

A significant advantage of the PLM is in the differentiation and recognition of various forms of the same chemical substance polymorphic forms, eg, brookite, mtile, and anatase, three forms of titanium dioxide calcite, aragonite and vaterite, all forms of calcium carbonate Eorms I, II, III, and IV of HMX (a high explosive), etc. This is an important appHcation because most elements and compounds possess different crystal forms with very different physical properties. PLM is the only instmment mandated by the U.S. Environmental Protection Agency (EPA) for the detection and identification of the six forms of asbestos (qv) and other fibers in bulk samples. 

Polypropylene polymers are typically modified with ethylene to obtain desirable properties for specific applications. Specifically, ethylene—propylene mbbers are introduced as a discrete phase in heterophasic copolymers to improve toughness and low temperature impact resistance (see Elastomers, ETHYLENE-PROPYLENE rubber). This is done by sequential polymerisation of homopolymer polypropylene and ethylene—propylene mbber in a multistage reactor process or by the extmsion compounding of ethylene—propylene mbber with a homopolymer. Addition of high density polyethylene, by polymerisation or compounding, is sometimes used to reduce stress whitening. In all cases, a superior balance of properties is obtained when the sise of the discrete mbber phase is approximately one micrometer. Examples of these polymers and their properties are shown in Table 2. Mineral fillers, such as talc or calcium carbonate, can be added to polypropylene to increase stiffness and high temperature properties, as shown in Table 3. 

Calcium carbonate, available both from natural sources and as precipitated forms (see Calcium compounds), is most useful in coating because of purity and high brightness, ie, 90—95%. Ground carbonates from marble deposits have high purity levels as do the carbonates from some chalk deposits. 

The mbber compound usually requires an inert inorganic filler and small particle sise carbon particle for reinforcement. The mbber polymers vary in inherent tensile strength from very high in the case of natural mbber to almost nonexistent for some synthetic polymers, eg, SBR. The fillers most commonly used for mbber compounds include carbon black, clay, calcium carbonate, siUca, talc (qv), and several other inorganic fillers. 

The selection of boiler-water treatment is also dependent on the type of cooling water. When cooling water reaches the boiler, various compounds precipitate before others. For instance, seawater contains considerable magnesium chloride. When the magnesium precipitates as the hydroxide, hydrochloric acid remains. In some lake waters, calcium carbonate is a significant impurity. When it reaches the boiler, carbon dioxide is driven off in the... 

Although they may be completely soluble in the lower temperature bulk water, these compounds (eg, calcium carbonate, calcium phosphate, and magnesium siUcate) supersaturate in the higher temperature water adjacent to the heat-transfer surface and precipitate on the surface. 

The lime or lime—soda process results in the precipitation of calcium as calcium carbonate and magnesium as magnesium hydroxide. The solubiUties of these compounds are shown in Figure 4 as functions of pH. When lime is used alone, only the carbonate hardness is reduced. The carbonate hardness is present as calcium or magnesium bicarbonate. The additional use of soda ash can reduce the noncarbonate hardness by providing additional carbonate ion. The reactions involved in the various steps of the process are Hsted below ... 

Calcium carbonate is finding increasing use in flue gas desulfurization. This appHcation by a variety of engineering processes traps the sulfur—oxygen compounds produced in the combustion of coal (qv) (see Coal conversion process Exhaust contdol, industrial Sulfurremoval and recovery). 

Chalk is a calcium carbonate prepared by precipitation. It is used in many polishing compounds including dentifrices. 

Mineral fillers are used for light-colored compounds. Talc has a small particle size and is a semireinforcing filler. It reduces air permeabihty and has htde effect on cure systems. Calcined clay is used for halobutyl stoppers in pharmaceutical appHcations. Nonreinforcing fillers, such as calcium carbonate and titanium dioxide, have large particle sizes and are added to reduce cost and viscosity. Hydrated siUcas give dry, stiff compounds, and their acidity reduces cure rate hence, their content should be minimized. 

Carbon blacks are usually used as fillers. The semi-reinforcing types, such as PEP (Past Extmsion Pumace) and SRE (Semi-Reinforcing Pumace) give the best performance (see Carbon, carbonblack). To lower the cost and improve the processibiUty of light compounds, or to lower the cost of black compounds, calcined clay or fine-particle calcium carbonate are used. 

Particulate fillers are divided into two types, inert fillers and reinforcing fillers. The term inert filler is something of a misnomer as many properties may be affected by incorporation of such a filler. For example, in a plasticised PVC compound the addition of an inert filler will reduce die swell on extrusion, increase modulus and hardness, may provide a white base for colouring, improve electrical insulation properties and reduce tackiness. Inert fillers will also usually substantially reduce the cost of the compound. Amongst the fillers used are calcium carbonates, china clay, talc, and barium sulphate. For normal uses such fillers should be quite insoluble in any liquids with which the polymer compound is liable to come into contact. 

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