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Silica estimation

Poly(vinyl pyrrolidone) (pharmaceutical purity) (-CH2 CH(NC4H60)-) , n 100, molecular weight of 12600 2700, was used as received. The PVP solution was added to the BMS of silica, or fumed silica powder was added to the PVP solution then agitated (1000 rpm) for several hours, then sonicated for 5-6 min. The ratio between the concentrations y= Cpyp/Csio was between 0 and 1, and 7 < 0.1 corresponds to practically irreversible adsorption of PVP, as it is not washed from silica. Estimated statistical monolayer (0=1) corresponds to y 0.2. Several experiments with PVP/silica were performed using the physiological buffer solution (PBS) with NaCl... [Pg.501]

Functional efficacy prediction led to the discovery of two solvent candidates with excellent technical performance. Laboratory tests confirmed the in silica estimation and found an excellent efficiency when metal parts were degreased by immersion and subsequently rinsed with water. [Pg.418]

FIGURE 4.36 Primary nanoparticle size distributions of silicas estimated from the adsorption data using the SCR procedure with the model of voids between spherical nanoparticles. (Adapted from A/ / /. Surf. ScL, 258, Gun ko, V.M., Zaulychnyy, Ya.V., Ilkiv, B.I. et al.. Textural and electronic characteristics of mechanochemically activated composites with nanosilica and activated carbon, 1115-1125,2011f, Copyright 2011, with permission from Elsevier.)... [Pg.570]

Sulphates may be determined in the filtrate from the silica estimation by precipitation with barium chloride solution, and weighing the barium sulphate, after filtering, and burning, expressing the result in terms of Na SO by the use of the factor 0 6094 . [Pg.133]

In Table 5.3, is compared with the total hydroxyl concentration (Ni, + N ) of the corresponding fully hydroxylated, sample. The results clearly demonstrate that the physical adsorption is determined by the total hydroxyl content of the surface, showing the adsorption to be localized. It is useful to note that the BET monolayer capacity n JH2O) (= N ) of the water calculated from the water isotherm by the BET procedure corresponds to approximately 1 molecule of water per hydroxyl group, and so provides a convenient means of estimating the hydroxyl concentration on the surface. Since the adsorption is localized, n.(H20) does not, of course, denote a close-packed layer of water molecules. Indeed, the area occupied per molecule of water is determined by the structure of the silica, and is uJH2O) 20A ... [Pg.274]

Transparent fused silica can be formed at a temperature of 1200°C and a pressure of 13.8 MPa (2000 psi) from silica powder consisting of 15 nm ultimate particles (92) or by electric arc fusion of pure silica sand having low iron and alkali metal contents. The cooled product is ground to the desired particle size. Fused sihca is primarily manufactured by C-E Minerals, Minco, and Precision Electro Minerals in the United States by Chuo Denko, Denki Kagaku Kogyo, NKK, Showa Denko, and Toshiba Ceramics in Japan. Based on 1988 data and projected growth, an estimated 135,000 metric tons of fused siUca were used in 1994 as a sacrificial component or investment casting in the manufacture of metals and as a component in refractory materials (62). [Pg.494]

Heat Capacity. The mean heat capacity (0—900°C) at constant pressure, 6, in J/(kg- " C), can be estimated in vitreous silica using the following expression, where / is temperature in °C. [Pg.505]

These ate the main reactions ia Pordand cements because the two calcium siHcates constitute about 75% of the cement. The average lime—silica ratio (C S) may vary from about 1.5 to about 2.0 or even higher, the average value is about 1.7. The water content varies with the ambient humidity, the three moles of water being estimated from measurements ia the dry state and stmctural considerations. As the lime—silica ratio of the C—S—H iacreases, the amount of water iacreases on an equimolar basis, ie, the lime goes iato the stmcture as calcium hydroxide, resulting ialess free calcium hydroxide. [Pg.287]

She et al. [128] used rolling contact to estimate the adhesion hysteresis at polymer/oxide interfaces. By plasma oxidation of the cylinders of crosslinked PDMS, silica-like surfaces were generated which could hydrogen bond to PDMS r olecules. In contrast to unmodified surfaces, the adhesion hysteresis was shown to be larger and proportional to the molecular weight of grafted polymer on the substrate. The observed hysteresis was interpreted in terms of the orientation and relaxation of polymer chains known as Lake-Thomas effect. [Pg.133]

A major step in catalyst development was the introduction of crystalline zeolitic, or molecular sieve catalysts. Their activity is very high, some of the active sites being estimated at 10,000 times the effectiveness of amorphous silica-... [Pg.16]

The dried polyoxazoline-modified silica gel was immersed into distilled water. The adsorption property of the resulting gel was estimated by the water content. The water uptake was calculated from an expression of (W -W)jW, where Wis the weight of dried gel and W is the weight of water-absorbed gel. The modified gel showed a higher water-adsorption property than that of untreated silica gel, which absorbed 10.8 multiples of water. The water uptake of modified gel was up to 13.7 multiples of the weight of dried gel. Thus, silica gel has been made more hydrophilic by a polyoxazoline segment. [Pg.24]

After extraction of the neutral oil from the AOS sample, the neutral oil is made up volumetrically to at least a 10% solution in hexane. Of this solution 4 pi is spotted onto a silica gel TLC plate, together with terminal 5-sultone standard in the range 0.4-4 pg (equivalent to 0.1-1% sultone in the neutral oil). It is twice developed in a chamber saturated with 2-propyl ether. The solvent is completely evaporated and the spots visualized by vapor phase sulfuric acid charring using the technique described by Martin and Allen [139]. Humidity is not critical (10-30% is optimum) and activation of the plates has not been found necessary, but it might be required under conditions of high humidity. The level of sultone can be estimated by visual comparison with the standards or by the use of a densitomer. [Pg.450]

Use the VSEPR model to estimate the Si—O—Si bond angle in silica. [Pg.740]

For silica an additional component of silicic acid generated by inorganic dissolution also occurs. One can estimate oxidized" Si as being 23/138 AOU, but discrimination between preformed Si and inorganic Si is not possible. Representative profiles of PO4, NO3, and Si are given in Fig. 10-19. Note that after subtracting the oxidative nutrients the preformed values are relatively constant. [Pg.263]

An attempt has also been made for qualitative estimation of the interaction at the rubber-silica interfaces. This has been accomplished by recording the solution viscosity of the precursor sols of these hybrid composites continuously for five days, with an interval of 24 h in the course of in situ silica generation. Figure 3.21 shows the result. [Pg.77]

Figure 2. Estimated rates of oxygen uptake by samples of silica-supported PVl (circles), PV3 (triangles) and PV14 (diamonds). Approach to saturation was modeled as either first-order kinetics (solid line, x =0.054) or second-order kinetics (dashed line, y =0.585). Figure 2. Estimated rates of oxygen uptake by samples of silica-supported PVl (circles), PV3 (triangles) and PV14 (diamonds). Approach to saturation was modeled as either first-order kinetics (solid line, x =0.054) or second-order kinetics (dashed line, y =0.585).
The titration of silica-alumina acid sites with neodymium oxide is clearly seen in Figure 4. The relative acid strength, as estimated by the 2,3DMB2/4MP2 ratio during 2MP2... [Pg.566]

A TLC method was developed for the estimation of nieotinie aeid and nicotinamide (Fignre 10.7) in phatmacentical preparations containing other vitamins, enzymes, herbs, and drugs, etc. [16]. The percentage recoveries for nicotinic acid and nicotinamide were 100.1 + 1.9 and 100.2 1.5, respectively, with this system. Each alcohol extract of samples or standard was pnt on sihca gel TLC plates, which were developed with distilled water. Each silica gel spot visualized under UV lamp was collected and extracted with 0.1 mol/1 HCl. The optical density of each clear extract was measured at 262 run. [Pg.242]

Instead of using surrogate measures for oral absorption with a lipophilicity or permeability assay in vitro, oral absorption can also be estimated in silica by using... [Pg.29]


See other pages where Silica estimation is mentioned: [Pg.147]    [Pg.249]    [Pg.229]    [Pg.57]    [Pg.269]    [Pg.147]    [Pg.249]    [Pg.229]    [Pg.57]    [Pg.269]    [Pg.577]    [Pg.488]    [Pg.284]    [Pg.274]    [Pg.250]    [Pg.55]    [Pg.118]    [Pg.482]    [Pg.504]    [Pg.575]    [Pg.155]    [Pg.93]    [Pg.620]    [Pg.162]    [Pg.166]    [Pg.449]    [Pg.295]    [Pg.322]    [Pg.438]    [Pg.185]    [Pg.186]    [Pg.65]    [Pg.661]    [Pg.66]    [Pg.107]    [Pg.285]    [Pg.331]   
See also in sourсe #XX -- [ Pg.415 , Pg.416 ]




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