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High viscosity polymers

PET suitable for bottle manufacture is produced by a modified process. Here the high-viscosity polymer melt is subjected to a rapid quenching in water to produce clear amoiphous pellets. These are further polymerised in the solid phase at temperatures just below the T . This is useful to reduce aldehyde content, since aldehyde-forming degradation reactions occur less in the lower temperature solid phase polymerisations. Aldehydes can impart a taste to beverages and it is important to keep the aldehyde content to below 2.5 p.p.m. [Pg.718]

Polymers melt over a range of temperatures, and polymers consisting of long chains tend to have high viscosities. Polymer strength increases with increasing chain length and the extent of crystallization. [Pg.889]

TXRF was used to characterize high-viscosity polymer dispersions [83], with special attention being paid to the different drying techniques and their effect on the uniformity of the deposited films. TXRF was also used as a means to classify different polymers on the basis of their incoherently scattered peaks [84], Dispersive XRF has been used to assess the level of aluminum in antacid tablets [85]. [Pg.228]

Plastic explosives, such as dynamites, are explosives rich in a liquid constituent, e.g. nitroglycerine, usually with dissolved high viscosity polymers. Guhr dynamite (no more in use) composed of 75% nitroglycerine and 25% kieselguhr, the first explosive to have a plastic consistency, owed this property to the high proportion of liquid it contained. [Pg.281]

Screw pumps [Fig. 7.12(g)] are suited for example to high viscosity polymers and dirty liquids at capacities up to 2000 gpm and pressures of 200 atm at speeds up to 3000 rpm. They are compact, quiet, and efficient. Figure 7.4(d) shows typical performance data. [Pg.143]

Several wholly aromatic polyamides have been prepared by use of triphenyl phosphite in NMP-pyridine solution containing 4 wt-% LiCl (Table 3). The combination of isophthalic acid with diamines gives a polymer of high viscosity whereas tere-phthalic acid (TPA) with pKa values similar to those of isophthalic acid does not yield high-viscosity polymers. [Pg.9]

Therefore, it is necessary (1) to calculate real temperature fields in the production equipment during flow of curing mixtures with an allowance for specific rheological properties and real hydrodynamic situation (2) the tempCTature fields in the technological process are to be strictly controlled. These results stress the role and importance of meclmnical sources of heat and the necessity to take them into account in all production proceses where high-viscosity polymers or polymerizing liquids flow. [Pg.139]

The test instrument is tightly specified with respect to dimensions, tolerances, and temperature control. The die is 2.095 mm dia 0.005 mm by 8.00 mm long 0.025 mm. In addition to procedure A in which the extrudate is cut and weighed, a procedure B covers automatic measurement of distance and time for the piston movement. Although the MFR is expressed as g/lO min the cutoff time is specified between 240 and 5 seconds depending on the MFR range, i.e., for high-viscosity polymers, which extrude slowly, cutoff time is 240 seconds, whereas for low-viscosity polymers it is between 5 and 15 seconds. [Pg.185]

Under polymer synthesis there is considerable number of processes proceeding under phase separation conditions, in particular in such systems like "liquid-liquid" (high-viscosity polymer solution - low-molecular fluid), "gas-liguid" (polymer-analogous processes) and "solid-liquid" (catalytic polymerization). Necessity of substance transfer from one phase to another by mass-exchange [140], i.e. removal of diffusive limitations is the feature of heterogeneous processes. In this case one have to deal with serious problems while realizing fast chemical reactions [141]. [Pg.19]

An extruder is a suitable apparatus for handhng high-viscosity polymer melts continuously. Mixing of a polymer melt and supercritical CO2 takes place in an extruder because of the shear action and the convection mechanism. During this process, a single-phase solution forms, and the time needed is minimized because the shear actions in an extruder decreases the striation thickness and the diffusion distances. [Pg.266]

Similarly, the characterisation Fv 7 B 6 indicates a high-viscosity polymer-modified bituminous binder cut-back or fluxed material that contains a flux of vegetable origin, in which the recovered binder has a softening point higher than 50 C. [Pg.115]


See other pages where High viscosity polymers is mentioned: [Pg.325]    [Pg.114]    [Pg.77]    [Pg.210]    [Pg.371]    [Pg.301]    [Pg.774]    [Pg.80]    [Pg.459]    [Pg.99]    [Pg.90]    [Pg.476]    [Pg.500]    [Pg.189]    [Pg.100]    [Pg.547]    [Pg.641]    [Pg.301]    [Pg.90]    [Pg.169]    [Pg.1535]    [Pg.196]    [Pg.66]    [Pg.142]    [Pg.77]    [Pg.176]    [Pg.306]    [Pg.249]    [Pg.256]    [Pg.269]    [Pg.28]    [Pg.1012]   
See also in sourсe #XX -- [ Pg.23 ]




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