Silicate monomers

MgSi03). As in monomer silicates, bonding within chains is stronger than bonding between chains, which is between metal ions and non-bridging oxygens. 

Fig. 3 Raman spectra of independently verified monomer silicate solutions (3/a) model of Na4Si04, the hydrolized variations of which compose the dilute basic monomer solutions (3 ) model of the H2Na2Si04 molecule surrounded by 20 water molecules (3/c) and the computed and experimental Raman spectra of its dissociated H2Si04 " derivative likely present in dilute solutions of Na2Si03 x 9H2O [6] (3/d).

Silicate Glasses. Synthetic siHcates and siHca are composed of oligomers of the orthosiHcate ion, SiO. OrthosiHcate monomers have a... 

Fig. 1. Examples of stmctures for silicates (a) monomer where is present (b) metasilicates where is present and (c) branched-ring...

The way to think of them all is as Si04 tetrahedra (or, in polymer terms, monomers) linked to each other either directly or via a metal ion (M) link. When silica is combined with metal oxides like MgO, CaO or AI2O3 such that the ratio MO/SiOj is 2/1 or greater, then the resulting silicate is made up of separated Si04 monomers (Fig. 16.4a) linked by the MO molecules. (Olivene, the dominant material in the Earth s upper mantle, is a silicate of this type.)... 

Fig. 16.4. Silicate structures, (a) The Si04 monomer, (b) The Si207 dimer with a bridging oxygen. ( ) A chain silicate. (d) A sheet silicate. Each triangle is the projection of on Si04 monomer.

Vapour phase synthesis may be carried out by passing a mixture of acetylene and acetic acid through a reaction tube at 210-215°C. Typical catalysts for this reaction are cadmium acetate, zinc acetate and zinc silicate. The monomer in each of the above mentioned processes is purified by distillation. 

Silicone with vinyl-terminal groups is commonly UV-cured for release coatings. These materials have been combined with silicate tackifiers and acrylate monomers to make PSA compositions as well [55]. 

To accelerate the polymerization process, some water-soluble salts of heavy metals (Fe, Co, Ni, Pb) are added to the reaction system (0.01-1% with respect to the monomer mass). These additions facilitate the reaction heat removal and allow the reaction to be carried out at lower temperatures. To reduce the coagulate formation and deposits of polymers on the reactor walls, the additions of water-soluble salts (borates, phosphates, and silicates of alkali metals) are introduced into the reaction mixture. The residual monomer content in the emulsion can be decreased by hydrogenizing the double bond in the presence of catalysts (Raney Ni, and salts of Ru, Co, Fe, Pd, Pt, Ir, Ro, and Co on alumina). The same purpose can be achieved by adding amidase to the emulsion. 

In situ SAXS investigations of a variety of sol-gel-derived silicates are consistent with the above predictions. For example, silicate species formed by hydrolysis of TEOS at pH 11.5 and H20/Si = 12, conditions in which we expect monomers to be continually produced by dissolution, are dense, uniform particles with well defined interfaces as determined in SAXS experiments by the Porod slope of -4 (non-fractal) (Brinker, C. J., Hurd, A. J. and Ward, K. D., in press). By comparison, silicate polymers formed by hydrolysis at pH 2 and H20/Si = 5, conditions in which we expect reaction-limited cluster-cluster aggregation with an absence of monomer due to the hydrolytic stability of siloxane bonds, are fractal structures characterized by D - 1.9 (Porod slope — -1.9) (29-30). 

The initial transition of dissolved silicate molecules into solid nanoparticles is perhaps the least explored step in the synthesis of zeolites. One impediment to understanding this mysterious step is the poorly elucidated molecular composition of dissolved particles. The major mechanistic ideas for the formation of zeolites approach these structures differently i) many researchers believe that secondary building units (SBU) must be present to form initial nanoslabs [1,2] ii) some others prioritize the role of monomers to feed artificially introduced crystal nuclei or assume that even these nuclei form via appropriate aggregation of monomers [3] iii) silicate solutions are also frequently viewed as random mixtures of various siloxane polymers which condense first into an irregular gel configuration which can rearrange subsequently into a desired crystal nucleus at appropriate conditions [4,5],... 

Orthopedic devices, 3 721-735 joint replacement, 3 727-735 Orthopedic marrow needles, 3 743-744 Orthophosphate (PO4), in soil, 11 112 Orthophosphates, 18 830-841 20 637 magnesium, 18 839 manufacture of, 18 853-855 Orthophosphate salts, 18 836 Orthophosphoric acid, 18 815, 817-826 condensation of, 18 826 properties of, 18 817-819 solubility of boron halides in, 4 140t orf/zo-phthalic resins, 20 101, 113 formulation of, 20 102 Orthorhombic crystal system, 8 114t Orthorhombic phosphorus pentoxide, 19 49 Orthorhombic structure, of ferroelectric crystals, 11 95, 96 Orthorhombic symmetry, 8 114t Orthosilicate monomers, in silicate glasses, 22 453... 

The chemistry of silicone halides was recently reviewed by Collins.13 The primary use for SiCU is in the manufacturing of fumed silica, but it is also used in the manufacture of polycrystalline silicon for the semiconductor industry. It is also commonly used in the synthesis of silicate esters. T richlorosilane (another important product of the reaction of silicon or silicon alloys with chlorine) is primarily used in the manufacture of semiconductor-grade silicon, and in the synthesis of organotrichlorosilane by the hydrosilylation reactions. The silicon halohydrides are particularly useful intermediate chemicals because of their ability to add to alkenes, allowing the production of a broad range of alkyl- and functional alkyltrihalosilanes. These alkylsilanes have important commercial value as monomers, and are also used in the production of silicon fluids and resins. On the other hand, trichlorosilane is a basic precursor to the synthesis of functional silsesquioxanes and other highly branched siloxane structures. 

For moderate anodic potentials the dissolution rate becomes enhanced and the ratio of H2/Si is reduced due to the contribution of the electrochemical reaction path [Pa6]. At the electrode surface Si-H as well as Si-OH groups are present. For higher concentrations of the silicate monomer produced by reaction (4.3) silicate polymerization takes place [Ni6]. Passivation takes place for more anodic potentials, due to formation of Si-O-Si bonds according to reaction (4.2). 

Zhao and Brittain [280-282] reported the LCSIP of styrene on planar silicon wafers using surface modifications of 2-(4-(ll-triethoxysilylundecyl)phenyl-2-methoxy-propane or 2-(4-trichlorosilylphenyl)-2-methoxy-d3-propane respectively. Growth of PS brushes from these SAMs has been successfully achieved factors that influence PS thickness included solvent polarity, additives and TiC concentration. Sequential polymerization by monomer addition to the same silicate substrate bearing the Hving polymer chains resulted in thicker PS films. FTIR-ATR studies using a deuterated initiator indicated that the initiator efficiency is low, and the... 

Toyota works with karolin clay that has about a distance of 10 nm between the sheets. The clay is treated with caprolactam monomer that impregnates the clay sheets increasing the distance between sheets to 30-50 nm. The caprolactam monomer impregnating the silicate sheets is then polymerized giving nylon-silicate sheets. This sequence is illustrated in Figure 8.6. 

FIGURE 8.6 Silicate sheets impregnated with caprolactam monomer (M) that are eventually polymerized. 

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