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Polystyrene INDEX

While studying polymer distribution between the emulsion phases it was found that in the systems mentioned above obtained both by copolymerization of styrene with polybutadiene rubber and mixing styrene solutions of polymers when the composition is far enough from the critical mixing point, thermodynamic equilibrium is reached.At this thermodynamic equilibrium the ratio of polymer concentration (Cp) in rubber (index ) as well as in polystyrene (index ) phases is practically constant (table II),... [Pg.387]

MFI = melt flow index IV = intrinsic viscosity in CH2CI2 at 25°C From gel-permeation chromatography using polystyrene standards. [Pg.280]

DMPPO—polystyrene blends, because of the inherent flame resistance of the DMPPO component (oxygen index ca 29.5), can be made flame retardant without the use of halogenated additives that tend to lower impact strength and melt stabiUty in other polymers. Approximately one-half of total Noryl sales volume is in flame-retarded grades, ie, VO or VI in a 1.6-mm section (UL-94). [Pg.331]

As mentioned earlier, unmodified polystyrene first found application where rigidity and low cost were important prerequisites. Other useful properties were the transparency and high refractive index, freedom from taste, odour and toxicity, good electrical insulation characteristics, low water absorption and comparatively easy processability. Carefully designed and well-made articles from polystyrene were often found to be perfectly suitable for the end-use intended. On the other hand the extensive use of the polymers in badly designed and badly made products which broke only too easily caused a reaction away from the homopolymer. This resulted, first of all, in the development of the high-impact polystyrene and today this is more important than the unmodified polymer (60% of Western European market). [Pg.462]

Figure 4 Changes in (a) carbonyl index and (b) hydroxyl index versus irradiation time for polystyrene films. O-con-trol -2,4-DHBP -2H-4MBP -2H-4BB X-DHBP-F A-HMBP-F and D-HBBP-F. Figure 4 Changes in (a) carbonyl index and (b) hydroxyl index versus irradiation time for polystyrene films. O-con-trol -2,4-DHBP -2H-4MBP -2H-4BB X-DHBP-F A-HMBP-F and D-HBBP-F.
To run the residence time distribution experiments under conditions which would simulate the conditions occurring during chemical reaction, solutions of 15 weight percent and 30 percent polystyrene in benzene as well as pure benzene were used as the fluid medium. The polystyrene used in the RTD experiment was prepared in a batch reactor and had a number average degree of polymerization of 320 and a polydispersity index, DI, of 1.17. [Pg.304]

Silane radical atom transfer (SRAA) was demonstrated as an efficient, metal-free method to generate polystyrene of controllable molecular weight and low polydispersity index values. (TMSlsSi radicals were generated in situ by reaction of (TMSlsSiH with thermally generated f-BuO radicals as depicted in Scheme 14. (TMSlsSi radicals in the presence of polystyrene bromide (PS -Br), effectively abstract the bromine from the chain terminus and generate macroradicals that undergo coupling reactions (Reaction 70). [Pg.152]

In order to calculate particle size distributions in the adsorption regime and also to determine the relative effects of wavelength on the extinction cross section and imaginary refractive index of the particles, a series of turbidity meas irements were made on the polystyrene standards using a variable wavelength UV detector. More detailed discussions are presented elsewhere (23) > shown here is a brief summary of some of the major results and conclusions. [Pg.16]

Figure 11. Imaginary part of complex refractive index for polystyrene... Figure 11. Imaginary part of complex refractive index for polystyrene...
Published refractive index data for the mobile phase, polystyrene, polyacrylonitrile, and the two monomers were used to calculate refractive index detector calibrations for the two homopolymers. The published data were used to determine relationship between refractive index increments of monomer and corresponding homopolymer. Chromatographic refractometer calibrations for the two homopelymers were then calculated from experimentally measured calibration data for the two monomers. [Pg.81]

Molecular weights were measured by gel permeation chromatography on a Perkin-Elmer Series 10 Liquid Chromatograph using tetrahydro-furan as solvent and refractive index as the detection mode. Standards were polystyrene, and reported molecular weights for the poly-siloxanes do not include a correction. [Pg.251]

Gel permeation chromatography was performed in tetrahydrofuran using a Waters pump system and a Model 410 differential refractive index detector for the eluant. Five Ultrastyragel columns with nominal porosities ranging from 500 to 105 angstroms were used for all the samples and the polystyrene standards. [Pg.183]

No information on the cost of a specific polystyrene plant could be found in the literature. One 1969 source18, however, listed the average cost of a polystyrene plant as between 100 and 205 per annual ton. This will be extrapolated to 1974, using the Chemical Engineering Plant Design Index and an assumed inflation rate. [Pg.264]

Table 9E-9 lists unit operations in the polystyrene plant. The highest temperature is 400°F, in the extruder. From this and Figure 9-5, a temperature factor of 0.04 is obtained. There are no high pressures except in the extruder, and its value is unknown. The pressure factor will be assumed to be zero. Stainless steel is used, so the material factor is 0.2. From Equation 2 a complexity factor of 3.48 can be calculated. A direct process investment cost of 350,000 per functional unit is obtained from Figure 9-7. This means that the cost of constructing the plant when the Engineering News Record Construction Index (ENRCI) is 300 would be 3,150,000. This will be updated to 1960 when the ENRCI was 350, and then the CEPI will be used to obtain the cost in 1974. The resultant cost in 1974 is... [Pg.274]

The methods just presented can be used for any number of variables. However, optimizing all the possible variables of a plant in one massive optimization is a Herculean task. The usual approach is to reduce the number of variables to those that strongly affect the performance index. For instance, in the polystyrene example the cost of electricity is almost insignificant and can be ignored. However, the amount of water added to the reactor may be very important. An optimization is made for the major variables. Then the effects of the minor variables are considered either in groups or separately. [Pg.409]

Brominated phosphate is a very efficient flame retardant as measured by oxygen index and UL-94 (Table IX and Figure 4). The melt index of the resin does not change with the addition of brominated polycarbonate, doubles with brominated polystyrene, and doubles again with brominated phosphate (Table IX). [Pg.261]

The flame retardant performance of various flame retardant additives in a commercial polycarbonate/ABS alloy were compared. No antimony oxide was required. The data shows brominated phosphate to be a highly efficient flame retardant in this alloy (Table XI). An alloy composition containing 14% brominated phosphate and no antimony oxide gives a V-0 rating (Table XII). The melt index of this alloy containing 12% brominated polystyrene was 7.6 g/10 min. (at 250°C) the equivalent resin containing brominated phosphate had a melt index of 13.3 g/10 min. [Pg.261]


See other pages where Polystyrene INDEX is mentioned: [Pg.72]    [Pg.438]    [Pg.621]    [Pg.171]    [Pg.434]    [Pg.27]    [Pg.612]    [Pg.230]    [Pg.370]    [Pg.492]    [Pg.121]    [Pg.304]    [Pg.342]    [Pg.343]    [Pg.300]    [Pg.188]    [Pg.18]    [Pg.57]    [Pg.22]    [Pg.332]    [Pg.346]    [Pg.146]    [Pg.271]    [Pg.395]    [Pg.445]    [Pg.673]    [Pg.114]    [Pg.16]    [Pg.56]    [Pg.70]    [Pg.232]    [Pg.285]    [Pg.245]   


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