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Calcium bonding

Fig. 19. ORTEP view of CaCp2(Me3SiCCCCSiMe3) (conformer (B)) from an above perspective. The -SiMe3 groups are bent back from the metal center in both conformers. In conformer (B), three carbon atoms (C(6)-C(8)) are within 3.2 A of the metal center, whereas in conformer (A) a more symmetrical structure with the calcium bonding to two carbon atoms (C(7) and C(8)) is observed. (Redrawn from Ref. 104.)... Fig. 19. ORTEP view of CaCp2(Me3SiCCCCSiMe3) (conformer (B)) from an above perspective. The -SiMe3 groups are bent back from the metal center in both conformers. In conformer (B), three carbon atoms (C(6)-C(8)) are within 3.2 A of the metal center, whereas in conformer (A) a more symmetrical structure with the calcium bonding to two carbon atoms (C(7) and C(8)) is observed. (Redrawn from Ref. 104.)...
Electron affinity of fluorine First ionization potential of calcium Second ionization potential of calcium Lattice energy of fluorite Heat of sublimation of calcium Bond energy of fluorine... [Pg.93]

Principally calcium bonded to carboxyl groups in the macerals. [Pg.102]

Cooper and Castle have proposed a three-step sequence to explain the vitamin B12 absorption in the gastrointestinal tract. In the first step, vitamin B12 binds with the intrinsic factor in gastric juice. The affinity of the vitamin for the intrinsic factor is thought to be greater than its affinity for proteins in the intestinal content consequently, the intrinsic factor (IF) successfully displaces the vitamin from its weaker bonds with other proteins. Calcium facilitates and EDTA inhibits the absorption of vitamin B12 by the everted intestine. On the basis of these and related findings, workers proposed the second step in vitamin Bi2 absorption. At that stage it is assumed that the intrinsic factor-vitamin B12 complex is trapped in the intestinal wall by the intermediate of calcium bonds and absorbed by pinocytosis. This stage of the absorption process probably is interfered with in sprue and steatorrhea where calcicum soaps are formed in the intestinal lumen. [Pg.288]

Both objectives have been met by designing special hydrogenation catalysts The most frequently used one is the Lindlar catalyst, a palladium on calcium carbonate combi nation to which lead acetate and quinoline have been added Lead acetate and quinoline partially deactivate ( poison ) the catalyst making it a poor catalyst for alkene hydro genation while retaining its ability to catalyze the addition of H2 to the triple bond... [Pg.375]

Saccharin was discovered at Johns Hopkins Uni versity in 1879 in the course of research on coal tar derivatives and is the oldest artificial sweetener In spite of Its name which comes from the Latin word for sugar saccharin bears no structural relationship to any sugar Nor is saccharin itself very soluble in wa ter The proton bonded to nitrogen however is fairly acidic and saccharin is normally marketed as its water soluble sodium or calcium salt Its earliest applications were not in weight control but as a... [Pg.1051]

Phospha.tes. Many phosphates cl aim unique material advantages over siUcates that make them worth the higher material costs for certain apphcations. Glass-ceramics containing the calcium orthophosphate apatite, for example, have demonstrated good biocompatibiUty and, in some cases even bioactivity (the abiUty to bond with bone) (25). Recent combinations of fluorapatite with phlogopite mica provide bioactivity as well as machinability and show promise as surgical implants (26). [Pg.325]

Alloys suitable for castings that ate to be bonded to porcelain must have expansion coefficients matching those of porcelain as well as soHdus temperatures above that at which the ceramic is fired. These ate composed of gold and palladium and small quantities of other constituents silver, calcium, iron, indium, tin, iridium, rhenium, and rhodium. The readily oxidi2able components increase the bond strength with the porcelain by chemical interaction of the oxidi2ed species with the oxide system of the enamel (see Dental materials). [Pg.384]

Stabilization Mechanism. Zinc and cadmium salts react with defect sites on PVC to displace the labHe chloride atoms (32). This reaction ultimately leads to the formation of the respective chloride salts which can be very damaging to the polymer. The role of the calcium and/or barium carboxylate is to react with the newly formed zinc—chlorine or cadmium—chlorine bonds by exchanging ligands (33). In effect, this regenerates the active zinc or cadmium stabilizer and delays the formation of significant concentrations of strong Lewis acids. [Pg.549]

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... [Pg.92]

Zinc and calcium siUcates, and calcium tungstate doped with activators such an Mn, Pb, Sn, and Eu are just a few examples of a large number of known ionicaHy bonded luminescent pigments. HaUde phosphates of the general formula 3Ca(P0 2 CaX2, where X = F or Cl, and Sb " and are... [Pg.16]

Bioglasses are surface-active ceramics that can induce a direct chemical bond between an implant and the surrounding tissue. One example is 45S5 bioglass, which consists of 45% Si02, 6% 4.5% CaO, and 24.5% Na20. The various calcium phosphates have exceUent compatibUity with bone and... [Pg.176]

Sugar analysis by hplc has advanced greatly as a result of the development of columns specifically designed for carbohydrate separation. These columns fall into several categories. (/) Aminopropyl-bonded siHca used in reverse-phase mode with acetonitrile—water as the eluent. (2) Ion-moderated cation-exchange resins using water as the eluent. Efficiency of these columns is enhanced at elevated temperature, ca 80—90°C. Calcium is the usual counterion for carbohydrate analysis, but lead, silver, hydrogen, sodium, and potassium are used to confer specific selectivities for mono-, di-, and... [Pg.10]

Sihcon 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 sihcon carbide and a variety of compounds at relatively high temperatures. Sodium sihcate 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 sihcide. Sihcon carbide decomposes in fused alkahes such as potassium chromate or sodium chromate and in fused borax or cryohte, and reacts with carbon dioxide, hydrogen, ak, and steam. Sihcon carbide, resistant to chlorine below 700°C, reacts to form carbon and sihcon tetrachloride at high temperature. SiC dissociates in molten kon and the sihcon reacts with oxides present in the melt, a reaction of use in the metallurgy of kon 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 sihcon nitride-bonded type exhibits improved resistance to cryohte. [Pg.465]


See other pages where Calcium bonding is mentioned: [Pg.115]    [Pg.305]    [Pg.173]    [Pg.2203]    [Pg.97]    [Pg.125]    [Pg.115]    [Pg.305]    [Pg.173]    [Pg.2203]    [Pg.97]    [Pg.125]    [Pg.395]    [Pg.59]    [Pg.174]    [Pg.217]    [Pg.285]    [Pg.303]    [Pg.343]    [Pg.139]    [Pg.24]    [Pg.389]    [Pg.137]    [Pg.145]    [Pg.172]    [Pg.440]    [Pg.241]    [Pg.394]    [Pg.91]    [Pg.68]    [Pg.163]    [Pg.331]    [Pg.19]    [Pg.77]    [Pg.260]    [Pg.415]    [Pg.438]    [Pg.172]    [Pg.407]   


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Atomic bonds Calcium aluminate

Calcium clusters bonding state

Calcium direct bonding

Calcium fluoride, ionic bonding

Calcium sulfate-water bonds

Calcium-binding sites hydrogen bonds

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