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Hydrosilicate composition

Hydrosilicate Compositions Hydration/Pehydration. For the purpose of demonstrating the feasibility of the reconstitution process the work reported here used only cut discs or plates of sodium silicate glass. In this way the dimensions of the sample could be easily controlled and dealkalization data was more meaningful. In those cases where thermally molded items, such as lens shapes, were processed the results were identical. [Pg.280]

Figure 5 shows SEM scans of the porosity of dealkalized bodies from their surface to their central core. The original hydrosilicate had 18% Na20 and was dealkalized in 0.6M, NHi NOa. These pictures (5a) show that 24 hours at 80 C creates a broad gradient in pore size across the structure s cross section. On the other hand, one hour at 80 C followed by 23 hours at 50 C produces a more uniform pore structure (5b) in the same hydrosilicate composition. [Pg.285]

Carbosilane methacrylate oligomers were prepared in a two-step process. Initially a di-allyloxy intermediate was methacrylated using methacrylic anhydride to introduce a thermal crosslinker. Hydrosilation of this product was performed using chloroplatinic acid and sym-divinyltetramethyldisiloxane with 1,3- or 1,4-bis-dimethylsilylbenzene. The cationic photoinitiator diphenyl iodonium hexafluorophosphate was used to polymerize all blended compositions. [Pg.426]

For some systems, however, the influence of the temperature on the phase composition can be predicted based on chemical considerations. For instance, the composition of bismuth molebdatc catalysts is believed to be determined by the nature of the molybdate anion present in solution [28] which is dependent on the solution temperature. For Ni/SiCh catalysts the differences between catalysts prepared at high or low temperatures are explained by the formation of nickel hydrosilicate at high temperatures, while at low temperature the main precipitate is nickel hydroxide [29]. [Pg.41]

The possibility of mechanochemical reactions to occur via hydrothermal mechanism was demonstrated in [32] for the synthesis of calcinm hydrosilicates. Optimal water content values (humidity) of solid mixtures of correspondent hydrates were estimated for the achievement of local hydrothermal conditions (elevated temperature and pressure) in mechanochemical activators. It was shown experimentally that the main factor determining the kinetics and composition of the products was the molar fraction of the components, the same as for hydrothermal reactions, while the effect of temperatnre and pressnre was mnch weaker. [Pg.177]

H2O were prepared by either dehydrating commercial sodium silicate solutions or by autoclaving anhydrous glasses of comparable compositions. Regardless of their origin, dealkalization kinetics of these hydrosilicates favored high water content and lower alkali content. [Pg.285]

In our laboratory the motivation for the synthesis of di- and triblock copolymers was three-fold 1) synthesis of the organic blocks by a living polymerization technique such that segment length and copolymer composition could be controlled, 2) prevention of coupling of macromolecular species and 3) use of a technique that would allow for the synthesis of a plethora of copolymers based on variation of the organic monomer. Considering these qualifications, ATRP of vinyl monomers from mono- and difunctional PDMS macroinitiators was used. Scheme 3 illustrates the synthesis of ABA triblock copolymers from terminal functionalized PDMS. The method utilizes hydrosilation of attachable initiators to commercially available vinyl... [Pg.272]

TFVE Functional Silicones 4-6. Mono-olefin derivatives were reacted with a variety of commercial siloxane copolymers containing Si-H functionality by Pt(0) catalyzed hydrosilation methods. Polymer compositions containing varying amounts of TFVE were obtained based on the amount of Si-H linkages present in the copolymer (Figure 7). ... [Pg.315]

Thus, the process of solid-phase synthesis of fluoramphibole from either chemical reactants or pure natural silicates and hydrosilicates, i.e. compounds of stoichiometric compositions, was represented by multistep physicochemical interactions conventional for the formation of non-stoichiometric inorganic compounds (Rabenau, 1970). The mechanisms of this process were estimated by the properties of new phases emerged during the decomposition of hydrosilicates. [Pg.333]

To preview the progress in the field, completely new ligand classes such as dii-mines and N-heterocyclic carbenes have surfaced several lanthanides are established as quite effective catalysts asymmetric hydrosilation is now an extremely important tool in ehiral synthesis materials accessed via hydrosilation range from new block copolymers to POSS-based composites and dendrimers, and evidence is substantial that more than one type of catalytic cycle is operative for different transition metals or groups of transition metals and perhaps even for different oxidation states of some metals. [Pg.2]

The mechanical properties of porous concrete depends on macro structural defects and composition of calcium hydrosilicates. An exact estimation of these parameters is very important in porous concrete technology. [Pg.536]

These methods, along with analysis methods for determining the composition of calcium hydrosilicates (X-ray analysis, differential thermal analysis, etc.) do not demonstrate a direct relationship between macrostructure defectivity and mechanical properties. Thus, all of these methods can not be used to control technological processes. These parameters can not be taken into consideration as methods of analysis for solid phases calls for sophisticated instrumentation and equipment. [Pg.536]

The linear dimensions of the destructed layer and average ratio of the strength of the contact layer to the punch displacement (Rc/ ). The former allows the optimum pore size to be designed, the latter allows estimation of the influence of the features of the composition of calcium hydrosilicates on the strength of the concrete. From the experimental data it can be concluded that the perfect composition of calcium hydrosilicates gives the value of the previously mentioned ratio near 100. [Pg.540]


See other pages where Hydrosilicate composition is mentioned: [Pg.49]    [Pg.918]    [Pg.311]    [Pg.399]    [Pg.284]    [Pg.316]    [Pg.332]    [Pg.399]    [Pg.105]    [Pg.16]    [Pg.44]    [Pg.537]    [Pg.539]    [Pg.541]   


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