Polystyrene particle filler

The morphology of these two systems is shown in Figures 1 and 2, respectively. Figure 1 shows electron photomicrographs of fracture replicas of SBR vulcanizates containing polystyrene fillers of two different particles sizes, and the existence of the individual polystyrene particles is easily confirmed. Figure 2 shows a schematic of the morphology of a styrene-diene-styrene block copolymers, in which the formation of a... 

Very recently, the formation of clusters and filler network structures via interparticle interaction has also been observed in composites containing monodis-perse size crosslinked polystyrene particles [108]. 

Abrasion. Resistance to abrasion is adequate for many applications including footwear and can be improved hy addition of reinforcing pigments (hard clay, silicas, carbon blacks) and through use of added plastic materials such as polystyrene or polyolefins. Abrasion resistance is reduced by oils, seme resins and large-particle fillers. It is also improved with Increased molecular weight of the polymer (Table III). 

Additives used in final products Fillers calcium carbonate, calcium hydroxide, calcium oxide, carbon black, polymeric beads, polystyrene particles, zinc oxide Plasticizers 1-isobutyrate benzyl phthalate, 2,2,4-tri-methyl-1,3-pentanediol, alkyl sulfonic acid esters of phenol and/or cresol, benzyl butyl phthalate, chlorinated paraffins, hydrogenated perphenyl, isooctyl benzyl phthalate Curatives metal peroxides, oxy salts (e.g., dioxides of lead, manganese, calcium, etc.) ... 

Modification of filler s surface by active media leads to the same strong variation in viscosity. We can point out as an example the results of work [8], in which the values of the viscosity of dispersions of CaC03 in polystyrene melt were compared. For q> = 0.3 and the diameter of particles equal to 0.07 nm a treatment of the filler s surface by stearic acid caused a decrease in viscosity in the region of low shear rates as compared to the viscosity of nontreated particles more than by ten times. This very strong result, however, should not possibly be understood only from the point of view of viscometric measurements. The point is that, as stated above, a treatment of the filler particles affects its ability to netformation. Therefore for one and the same conditions of measuring viscosity, the dispersions being compared are not in equivalent positions with respect to yield stress. Thus, their viscosities become different. 

As a filler jn the elastomeric matrix of polysiloxane, spherical particles of polystyrene were also used and provided considerable reinforcement of the... 

Transition from liquid behavior to solid behavior has been reported with fine particle suspensions with increased filler content in both Newtonian and non-Newtonian liquids. Industrially important classes are rubber-modified polymer melts (small rubber particles embedded in a polymer melt), e.g. ABS (acrylo-nitrile-butadiene-styrene) or HIPS (high-impact polystyrene) and fiber-reinforced polymers. Another interesting suspension is present in plasticized polyvinylchloride (PVC) at low temperatures, when suspended PVC particles are formed in the melt [96], The transition becomes evident in the following... 

Reinforcing fillers can be deformed from their usual approximately spherical shapes in a number of ways. For example, if the particles are a glassy polymer such as polystyrene (PS), then deforming the matrix in which they reside at a... 

Under the conditions of Example 5-23 the rubber phase of the end product shows an interesting micro-morphology. It consists of particles of 1-3 microns diameter into which polystyrene spheres with much lower diameters are dispersed. These included polystyrene spheres act as hard fillers and raise the elastic modulus of polybutadiene. As a consequence, HIPS with this micro-morphology has a higher impact resistance without loosing too much in stiffness and hardness. This special morphology can be visualized with transmission electron microscopy. A relevant TEM-picture obtained from a thin cut after straining with osmium tetroxide is shown in Sect. 2.3.4.14. 

Although a majority of these composite thermistors are based upon carbon black as the conductive filler, it is difficult to control in terms of particle size, distribution, and morphology. One alternative is to use transition metal oxides such as TiO, VO2, and V2O3 as the filler. An advantage of using a ceramic material is that it is possible to easily control critical parameters such as particle size and shape. Typical polymer matrix materials include poly(methyl methacrylate) PMMA, epoxy, silicone elastomer, polyurethane, polycarbonate, and polystyrene. 

In more recent work, talc-filled polystyrene compounds, with various filler volume fractions, have been processed by compression moulding and through a variety of slit, capillary, rectangular and annular dies [37]. Particle orientation has been characterised using wide angle X-ray diffraction, then expressed in the form of pole figures, and by scanning electron microscopy. It was concluded that... 

Shear yield behaviour of polymer melts containing plate-like filler particles is also prevalent and is clearly shown in Fig. 8 for talc-filled polystyrene. In this system an estimate was made of shear yield values, which were found to increase with increasing particle loading and decreasing particle size. These results are compared with reported yield values for other particulate-filled polymers in Table 2. It is evident that shear yield values also depend on the particle type and thermoplastic matrix used. 

Figure 2.42 Viscosity increase as a function of volume fraction of filler for polystyrene and low density polyethylene containing spherical glass particles with diameters ranging between 36/.tm and 99.8 gm.

Composite density can be expected to vary because of the uneven distribution of filler particles in the manufactured product. This is very typical of the injection molding process where filler is distributed in a complex pattern of flow. In glass reinforced polystyrene parts, manufactured by injection molding, the density varied between 0.9 and 1.4 g/cm depending on the process conditions and locations Ifom which the sample was taken. ... 

For electrostatic and steric stabilization, the particles can be viewed effectively as colloids consisting of a soft and deformable corona surrounding a rigid core. Colloidal particles with bulk elastomeric properties are also available. These particles, which are generally of submicron size, are developed and used as reinforcement additives to improve the Impact resistance of various polymer matrices [28-30]. The rubber of choice is often a styrene/butadiene copolymer. The presence of chemical groups at the matrix-filler interface leads to improved adhesion between them. Typically, the addition of about 30% by volume of these elastomeric particles increases the impact strength of a brittle glassy polymer like polystyrene by up to a factor of 10. For some applications, particles with more complex architecture have been... 

U.S. Pat. No. 7,022,751 [111] describes a fiber-reinforced composite plastic material comprising thermoplastic polymers such as HDPE, LDPE, polypropylene, PVC, and polystyrene a high melting point waste polymer fiber material such as polyethylene terephthalate and nylon, an inorganic filler, such as glass and other material, and an organic filler such as wood or particles of a thermoset plastic, such as rubber and polyurethane foam. 

---