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Polymerisation speed

Figure 9 shows that increase in the excited state quencher concentration gives rise to an increased width of the reflection band. The fact that intensity plays a very important role indicates the competition between the phase separation process which causes the increase as opposed to the polymerisation speed which tends to freeze in the structure and the pitch present within the system. Such a pitch gradient has been observed in polymerized acrylate networks (9). In the case of studies of other gels, the band broadening occurred as the system phase separated into two regions containing liquid crystal and the liquid crystal swollen network. [Pg.287]

Silver and gold Silver is nearly always deposited from cyanide baths, though other baths have been described. To limit oxidation and polymerisation in high-speed selective plating with insoluble anodes, low-cyanide baths have been developed containing salts such as phosphate. ... [Pg.565]

Another study drew a comparison between the polymerisation of ethylene oxides and propylene oxides in similar operating conditions and in the presence of 10% of sodium hydroxide. When the polymerisation reached its maximum speed, the temperature reached 439°C for the former and 451 °C for the latter the pressures obtained are 44.6 and 26.6 bar respectively. [Pg.266]

Polymerisations at very low temperatures. The most spectacular feature of the cationic polymerisation of isobutene is the fact that it proceeds with great speed even at very low temperatures. Hitherto the lowest temperatures used were around -100°, but Kennedy and Thomas have extended the temperature range down to -185° in a series of highly ingenious experiments [60, 61]. [Pg.71]

The kinetics of the relatively fast polymerisation of the non-N-substituted NCA s initiated by LiCl in dimethyl formamide was thoroughly studied by Ballard, Bamford and Weymouth (44). Addition of this salt enormously speeded, by a factor of at least 1000, the extremely slow spontaneous polymerisation of glycine NCA. (In the absence of salt no reaction was detectable even after a few hours.) Other NCA s behaved similarly, although in the absence of the salt their spontaneous polymerisations were slightly faster than that of glycine NCA. The initial... [Pg.29]

After supplying silanol, the heating of apparatus 17 is switched on and the solvent is distilled, sending air through the bubble at the speed of 3 m3/h at 150 °C. The solvent vapours are condensed in cooler 11 and collected in receptacle 18. The distillation of the solvent occurs simultaneously with the condensation of silanol. During the distillation the temperature in apparatus 17 is increased to 170-200 °C, and the speed of air supply is raised to 30 m3/h. The mixture is periodically sampled to determine the viscosity and polymerisation time of the polymer. After the distillation air supply is stopped, the reactor receives a necessaiy amount of the solvent from batch box 10 and the mixture is cooled to 60 °C. The solution (var-... [Pg.325]

Lead tetraalkyl derivatives are used in catalytic systems to polymerise olefines, as catalysts of re-etherification and polycondensation, to speed up the alkylation of lateral chains of alkylbenzenes with ethylene and its derivatives. An addition of lead tetraalkyl derivatives (0.05-2% of alkylben-zene quantity) to catalysts of the liquid-phase oxidation of alkylbenzenes speeds up the oxidation. Tetraethyllead proved to be a good initiator for Diels-Alder reactions to join polymers with alkenylsiloxy chains and can be used as an additive to reduce the attrition and wear of rubbing metal parts. Tetrabutyllead is an active cross-linking agent for polyethylene and modifying agent for plastics. [Pg.488]

Fig. 40 Conducting film, plasma polymerised from 2-iodothiophene, on silicon. Left topography contrast (shaded pseudo-3D-image) with 405 nm corrugation. Middle real part (conductivity), with a contrast of 2.8 nA. Right imaginary part (capacity), with a contrast of 270 pA, the a.c. currents shown in the middle and in the right image were simultaneously measured together with the topography. The cantilever is made of silicon nitride coated with gold. The excitation is 0.8 V at 60 kHz, the scan speed is 4.17 pm/s... Fig. 40 Conducting film, plasma polymerised from 2-iodothiophene, on silicon. Left topography contrast (shaded pseudo-3D-image) with 405 nm corrugation. Middle real part (conductivity), with a contrast of 2.8 nA. Right imaginary part (capacity), with a contrast of 270 pA, the a.c. currents shown in the middle and in the right image were simultaneously measured together with the topography. The cantilever is made of silicon nitride coated with gold. The excitation is 0.8 V at 60 kHz, the scan speed is 4.17 pm/s...
Properties.—The pentoxide exists in crystalline and vitreous forms, the transformation temperature of which has been given as 440° C.5 Sublimation proceeds with moderate speed between 180° and 250° C.6 and the vapour pressure may reach 760 mm. at 860° C.7 When it is sublimed at 360° C. in a current of oxygen the oxide forms brilliant crystals together with some of the amorphous material which is considered to be a product of polymerisation. The crystalline form, by X-ray examination, is that of the rhombohedral system with 12P2Os in a unit cell the lengths of the axes are a = 11-12, b = 1-12 A.8... [Pg.131]

The polymeric adsorbents are usually prepared by variations of two-phase suspension processes. These refer to systems where microdroplets of monomers and solvent are converted into solid beads upon polymerisation. In the case where the monomers are not water soluble, as in the case of styrene-based polymers and many methacrylate-based polymers, the monomers, a solvent and a droplet stabiliser are suspended as droplets by stirring in water and then polymerised (o/w suspension polymerisation). The particle size and dispersity can be influenced by the stirring speed and the type of stabiliser. So far, only a few examples of the preparation of imprinted polymers in bead format have been described [4-8] and these are thoroughly reviewed in Chapter 12. In non-covalent imprinting, the main limitation to the use of these techniques is that the imprinting method often requires the use of polar partly water soluble monomers or templates in combination with less polar water insoluble components. Use of the o/w suspension method... [Pg.21]

Inverse opals are formed by the use of micro- or nanospheres to template a structure containing spherical cavities. One way of doing this is to use monodisperse latex spheres. These latex spheres are prepared by slow addition of an aqueous precursor solution into a reservoir of hydrophobic silicone liquid, forming emulsion droplets. The size of the droplets is controlled by the concentration of the aqueous latex, the speed at which the suspension is stirred and ratio between the silicone liquid and latex. Polymerisation results in latex spheres of well defined size of the order of a few hundred nanometers, and spherical shape. As the concentration of the latex spheres increases to its critical concentration... [Pg.906]

Polyacrylamide gels are prepared by copolymerisation of acrylamide monomer (CH2=CHCO NH2) with a cross linking agent, usually N, N-methylene bisacrylamide, CH2(NHCOCH = CH2)2, in the presence of a catalyst accelerator-chain initiator mixture. This mixture may consist of freshly prepared ammonium persulphate as catalyst (0.1 to 0.3% w/v) together with about the same concentration of a suitable base, for example, dimethylamino propionitrile (DMAP) or N, N, N, N tetramethylene diamine (TEMED) as initiator. TEMED is most frequently used and proportional increases in its concentration speed up the rate of gel polymerisation. Photochemical polymerisation may be brought about by riboflavin in the presence of UV radiation. Gelation is due to vinyl polymerisation as shown below ... [Pg.169]

The connection between speed of aggregation and extent of aggregation was examined. The mutations that led to the largest amount of fibrils after a 1 month incubation period were those that only had a very low P-sheet ratio initially. There thus seems to be a cormection between slow polymerisation and an enhancement in the extent of fibril formation. However, the pentapeptide STVn is known to be amyloidogenic, and mutations in the sixth position that accelerated amyloid formation also caused formation of large amounts of amyloid material. [Pg.45]

In a polymerisation reactor, a monomer/polymer solution is to be agitated in a baffled mixing vessel using a double turbine (6 fiat blades) impeller, with the configuration B-B in Table 8.1, at a rotational speed of 2Hz. The solution exhibits power-law behaviour with n = 0.6 and m = 12 Pa-s° . Estimate the power required for a 300 mm diameter impeller. The density of the solution is 950kg/m. ... [Pg.344]

Two-part adhesives in which the polymerisation catalyst is applied separately to the substrate prior to Joint assembly. Anaerobic peroxides may be incorporated to speed curing. Amines or nitrogen-free primers prepare the substrate and initiate the curing process. [Pg.464]

Tb = 0.23. This procedure offers significant advantages over classical methods for determining reactivity ratios in terms of its speed, ease of experimentation, and the fact that it utilises data obtained over the full range of conversion. It is anticipated that the technique will also be applicable to systems which deviate from the terminal model for polymerisation. [Pg.74]


See other pages where Polymerisation speed is mentioned: [Pg.414]    [Pg.93]    [Pg.158]    [Pg.414]    [Pg.93]    [Pg.158]    [Pg.169]    [Pg.251]    [Pg.355]    [Pg.236]    [Pg.291]    [Pg.643]    [Pg.1130]    [Pg.275]    [Pg.333]    [Pg.30]    [Pg.60]    [Pg.31]    [Pg.935]    [Pg.161]    [Pg.168]    [Pg.479]    [Pg.154]    [Pg.444]    [Pg.313]    [Pg.256]    [Pg.700]    [Pg.189]    [Pg.27]    [Pg.128]    [Pg.138]    [Pg.44]    [Pg.21]    [Pg.317]    [Pg.236]    [Pg.504]   
See also in sourсe #XX -- [ Pg.50 ]




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