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Viscosity of melts

We will now turn our attention from the viscosity of dilute solutions and look at the viscosity of melted polymers. The viscosity of melted polymers is important in transferring resins and in polymer processing such as determining the correct conditions to have a specific flow rate for injection processing and in determining the optimum conditions to get the necessary dimensions of extruded shapes. Fillers, plasticizers, temperature, solvents, and molecular weight are just some of the variables that influence the viscosity of polymer melts. Here we will look at the dependence of melt viscosity on polymer molecular weight. Polymer melts have viscosities on the order of 10,000 MPa (1 centipoise =0.001 Pa/sec). [Pg.77]

This is suitable for the formulations in which the percentage of solid ingredients, suspended in liquid is to be increased. The advantage of density difference between the molten medium and suspended particles is used in this process. The concentration of heavier particles is increased in the lower part of the casing either by natural sedimentation or by forced sedimentation caused by vibrating the whole casting assembly. The sedimentation process is controlled by a number of parameters such as particle size of solid suspension, temperature of melt, period of sedimentation, viscosity of melt, concentration of solid ingredients and column of melt etc. [Pg.166]

Batch (preparation of agglomerating liquid) Duration of viscous-plastic state at 140 °C, s Viscosity of melted compound, p 10-9 Pa. s at 140 °C Flow, mm Bulk density g/m3 Looseness, s Content of methylol groups, 0/ Granulometric composition, % ... [Pg.170]

The charge of material placed into each cavity is known as a preform. Unlike the lower viscosity of melt injected in conven-... [Pg.503]

FIG. 132. Viscosity of melts in the system K2O—Si02 (Frohberg and Rohde, 1964). [Pg.100]

The phase diagram of the system KiO —Si02 is shown in Fig. 131, the viscosity of melts in this system is plotted in Fig. 132. Figures 133 and 134 present similar data on the system PbO —SiOa-... [Pg.101]

The relationships between the viscosity of melts (liqu ds), the diffusion phenomena and the rate of crystal growth have been the subject of numerous theoretical and experimenal Siudies (cf. Frenkel, 1945 Doremus, 1973). A useful practical parameter is provided by the product uij) which forsimple oxides(Si02, GeO, P205>is proportional to undercooling AT= Tjiq — T. It therefore holds that... [Pg.252]

The viscosity of melts in the system Na20 —SiOj is shown in Fig. 125. The composition of binary glasses can be estimated roughly from density using the diagram in Fig. 126. [Pg.311]

The compound albite, Na20 A1203 6SiOz, melts congruently at 1118 3°C. For those compositions in the albite field with a Iiquidus of about 1040°C or less, albite crystallized in a few days at a temperature 50 to 75° below Iiquidus temperatures. To the left of the carnegieite-silica line, a rapid decrease in the viscosity of melts in the albite field occurs. As a result, it is possible to crystallize albite even at temperatures around 750°C. In the albite field toward the system albite-silica, crystallization of albite is very difficult. [Pg.50]

The method of falling body is used with advantage for the simultaneous measurement of density and viscosity of melts with the viscosity in the range from 1 to 10 Pa s. The measurement is based on Stokes law. The principle of this method is to measure the speed of a partially counter-balanced body, which moves up or down in the melt, depending on whether the body is under-balanced or over-balanced. [Pg.377]

Molecular Meaning of aM. The dependence of the reduced viscosity of melt polymers on molecular weight is given by... [Pg.190]

Thickness is related to the viscosity of melting ice cream before swallowing. [Pg.132]

Results represented in Tables 3 and 4 show that the frictional component of the viscosity ri very strongly depends on the length of the polymeric chains and on the temperature. The whole spectrum of the dependence of Tj on N and T will be considered as the superposition of the above earlier listed three forms of the motion which make the endowment into the frictional component of the viscosity of melt, namely the frictional coefficients of viscosity t], and see Chapter 2.2.). [Pg.155]

Explain why the viscosities of melts which form network glasses often vary more slowly with temperature than do the viscosities of ionic melts. [Pg.137]

The basic principles for the transport of macromolecules in dilute solution will be discussed in this section these principles will be utilized for molar mass determinations in Section 9. In addition, the viscosities of melts and concentrated solutions will also be treated, but the determination of molar masses by relative viscosities will not be treated here, but in Section 9. It is also more appropriate to treat heat conduction with the thermal properties of polymers in Section 10. [Pg.251]

Large to very large, idiomorphic alite crystals Correlated with increasing SO3 content in low-alkali laboratory clinkers reduced viscosity of melt strength loss (Dreizier, Strunge, and Knofel, 1985)... [Pg.74]

Increase in alite size and idiomorphism Lowered viscosity of melt resulting from increase in clinker sulfate and degree of sulfatization (sulfate to alkali ratio) (Strunge, Knofel, and Dreizier, 1985)... [Pg.76]


See other pages where Viscosity of melts is mentioned: [Pg.23]    [Pg.285]    [Pg.82]    [Pg.112]    [Pg.74]    [Pg.194]    [Pg.109]    [Pg.93]    [Pg.146]    [Pg.81]    [Pg.485]    [Pg.324]    [Pg.99]    [Pg.54]    [Pg.177]    [Pg.431]    [Pg.534]    [Pg.441]    [Pg.155]    [Pg.157]    [Pg.144]    [Pg.45]    [Pg.125]    [Pg.128]    [Pg.135]    [Pg.9]    [Pg.78]    [Pg.268]    [Pg.271]    [Pg.48]    [Pg.317]   
See also in sourсe #XX -- [ Pg.19 , Pg.48 , Pg.218 ]

See also in sourсe #XX -- [ Pg.81 ]




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