Magnesium silicate used with carbon

Alternatively, as described in U.S. Patent 3,341,557, 6-dehydro-17-methyltestosterone may be used as the starting material. A mixture of 0.4 g of cuprous chloride, 20 ml of 4 M methylmagnesium bromide in ether and 60 ml of redistilled tetrahydrofuran was stirred and cooled in an ice bath during the addition of a mixture of 2.0 g of 6-dehydro-l 7-methyl-testosterone, 60 ml of redistilled tetrahydrofuran and 0.2 g of cuprous chloride. The ice bath was removed and stirring was continued for four hours. Ice and water were then carefully added, the solution acidified with 3N hydrochloric acid and extracted several times with ether. The combined ether extracts were washed with a brine-sodium carbonate solution, brine and then dried over anhydrous magnesium sulfate, filtered and then poured over a 75-g column of magnesium silicate (Florisil) packed wet with hexanes (Skellysolve B). The column was eluted with 250 ml of hexanes, 0.5 liter of 2% acetone, two liters of 4% acetone and 3.5 liters of 6% acetone in hexanes. 

Isolation of the active component is carried out chro-matographically. Roth et al.9 used a magnesol (magnesium silicate) column to absorb colored impurities, followed by a Darco G-60 activated carbon column to eliminate sodium formate and inorganics. Elution with an alcohol/ammonia solvent was followed by rechromatographing in magnesol. 

Silicon carbide is comparatively stable. The only violent reaction occurs when SiC is heated with a mixture of potassium dichromate and lead chromate. Chemical reactions do, however, take place between silicon carbide and a variety of compounds at relatively high temperatures. Sodium silicate attacks SiC above 1300°C, and SiC reacts with calcium and magnesium oxides above 1000°C and with copper oxide at 800°C to form the metal silicide. Silicon carbide decomposes in fused alkalies such as potassium chromate or sodium chromate and in fused borax or cryolite, and reacts with carbon dioxide, hydrogen, air, and steam. Silicon carbide, resistant to chlorine below 700°C, reacts to form carbon and silicon tetrachloride at high temperature. SiC dissociates in molten iron and the silicon reacts with oxides present in the melt, a reaction of use in the metallurgy of iron and steel (qv). The dense, self-bonded type of SiC has good resistance to aluminum up to about 800°C, to bismuth and zinc at 600°C, and to tin up to 400°C a new silicon nitride-bonded type exhibits improved resistance to cryolite. 

At present, many studies are ongoing to identify a means of enhancing the carbonation chemistry of magnesium silicates in aqueous systems, using weak acids and additives that will improve silica dissolution, such as citrates, oxalates, and EDTA [105, 111]. In this case, a near-complete recovery and reuse, thereby minimizing the losses of such chemicals, will be essential for viable process economics. Likewise, there is much to improve with regards to the reaction rates and/ or times. 

The total surface concentration and intensity distribution of acidic and basic active sites are presented in Fig. 7.10. The total height of the stacked bars represents the total surface concentration of the acidic and basic active sites in millimoles per gram. The individual parts of the stacked bar correspond to the intensity distribution. As shown in Fig. 7.10, these data indicate that magnesium silicate has a total acidic and basic site concentration of 1.8 and 2.3 mM/g, respectively [17]. In comparison with other types of adsorbents used in frying oil (activated carbon, alumna [basic], alumina [neutral], alumina [acidic], bleaching earth, dia-tomaceous earth, and silica), magnesium silicate shows the highest values of total acidic and basic sites. 

Fillers are materials that modify rubber characteristics (e.g., hardness) and improve its physical characteristics (e.g., tensile strength), in addition to reducing costs. Rubber is sometimes compounded without the use of fillers the resultant product is called gum rubber. Typical fillers are calcined and hydrated clays, magnesium silicate (talc), magnesium oxide, and silicas. Carbon black, a common filler used to increase the heat resistance in industrial components such as tires, is not used as a filler in pharmaceutical components but it is used in smaller amounts as a black pigment. Polynuclear aromatic (PNA) hydrocarbons are a concern with carbon blacks but the grades used by manufacturers of pharmaceutical components contain very low concentrations. 

Use a hard granular carbon that can withstand peptizing action Apply carbon in an admixture with another adsorbent such as magnesium silicate, bentonite, activated clay. In selecting an additional adsorbent it is necessary to consider whether the pH and other characteristics are compatible with the system being treated Conduct the adsorption in separate stages ... 

Magnesium silicate and bentonite, when used with activated carbon in aqueous solution, are reported to aid filtration and settling and also to minimize peptization of the carbon. 

Inorganic colorants listed in 21CFR 178.3297 include aluminum, aluminum hydrate, potassium silicate, aluminum silicate, barium sulfate, bentonite, calcium carbonate, calcium silicate, calcium sulfate, carbon black (channel process, prepared by the impingement process from stripped natural gas), chromium oxide green Cr203, cobalt aluminate (with restrictions), diatomaceous earth, iron oxides, kaolin (modified for use in olefin polymers in amounts up to 40%), magnesium oxides, magnesium silicate (talc), sienna, silica, titanium dioxide, titanium dioxide-barium sulfate, ultramarines, zinc carbonate (limited use), zinc chromate (less than 10%), zinc oxide (limited use), and zinc sulfide (less than 10%). 

Examples of inert or extender fillers include china clay (kaolin), talc, and calcium carbonate. Calcinm carbonate is an important filler, with a particle size of about 1 pm. It is a natural product from sedimentary rocks and is separated into chalk, limestone, and marble. In some cases, the calcium carbonate may be treated to improve interaction with the thermoplastic. Glass spheres are also used as thermoplastic fillers. They may be either solid or hollow, depending on the particular application. Talc is a filler with a lamellar particle shape. It is a namral, hydrated magnesium silicate with good slip properties. Kaolin and mica are also natural materials with lamellar structures. Other fillers include woUastonite, silica, barium sulfate, and metal powders. Carbon black is used as a filler primarily in the rnbber industry, but it also finds application in thermoplastics for conductivity, for UV protection, and as a pigment. Fillers in fiber form are often used in thermoplastics. Types of fibers inclnde cotton, wood flour, fiberglass, and carbon. Table 1.3 shows the fillers and their forms. An overview of some typical fillers and their effect on properties is shown in Table 1.4. Considerable research interest exists for the incorporation of nanoscale fillers into polymers. This aspect will be discussed in later chapters. 

Calcium carbonate is an important filler with a particle size of about 1 p,m. It is a natural product from sedimentary rocks and is separated into chalk, limestone, and marble. In some cases the calcium carbonate may be treated to improve the bonding with the thermoplastic. Glass spheres are also used as thermoplastic fillers. They may be either solid or hollow, depending on the particular application. Talc is an important filler with a lamellar particle shape. It is a natural hydrated magnesium silicate with good slip properties. Kaolin and mica are also natural materials with lamellar stracture. Carbon black is used as a filler primarily in the rubber industry. 

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