Polystyrene crystalline

Pure amorphous polymers, being homogeneous materials, are transparent. Atactic polystyrene is a good example. The crystalline syndiotactic form is not transparent. Alack of transparency does not necessarily indicate crystallinity, however. It can also be caused by inorganic fillers, pigments, gas bubbles (as in a foam), a second polymer phase, etc. 

Carbon Cha.in Backbone Polymers. These polymers may be represented by (4) and considered derivatives of polyethylene, where n is the degree of polymeriza tion and R is (an alkyl group or) a functional group hydrogen (polyethylene), methyl (polypropylene), carboxyl (poly(acryhc acid)), chlorine (poly(vinyl chloride)), phenyl (polystyrene) hydroxyl (poly(vinyl alcohol)), ester (poly(vinyl acetate)), nitrile (polyacrylonitrile), vinyl (polybutadiene), etc. The functional groups and the molecular weight of the polymers, control thek properties which vary in hydrophobicity, solubiUty characteristics, glass-transition temperature, and crystallinity. 

Styrene [100-42-5] (phenylethene, viaylben2ene, phenylethylene, styrol, cinnamene), CgH5CH=CH2, is the simplest and by far the most important member of a series of aromatic monomers. Also known commercially as styrene monomer (SM), styrene is produced in large quantities for polymerization. It is a versatile monomer extensively used for the manufacture of plastics, including crystalline polystyrene, mbber-modifted impact polystyrene, expandable polystyrene, acrylonitrile—butadiene—styrene copolymer (ABS), styrene—acrylonitrile resins (SAN), styrene—butadiene latex, styrene—butadiene mbber (qv) (SBR), and unsaturated polyester resins (see Acrylonithile polya rs Styrene plastics). 

The regular syndiotactic and isotactic structures are capable of crystallisation whereas the atactic polymer carmot normally do so. In the case of polypropylene the isotactic material is a crystalline fibre-forming material. It is also an important thermoplastic which can withstand boiling water for prolonged periods. Atactic polypropylene is a dead amorphous material. Polystyrene as commonly encountered is atactic and glass-like but the syndiotactic material... 

Some interesting differences are noted between amorphous and crystalline polymers when glass fibre reinforcement is incorporated into the polymer. In Figure 9.2 (ref. 10) it will be seen that incorporation of glass fibre has a minimal effect on the heat deflection temperature of amorphous polymers (polystyrene,... 

In the late 1990s a crystalline form of polystyrene, syndiotactic polystyrene became commercially available but unless otherwise stated references to polystyrene in this chapter will refer to the traditional amorphous polymer. 

Because of the chain-stiffening effect of the benzene ring the TgS of commercial materials are in the range 90-100°C and isotactic polymers have similar values (approx. 100°C). A consequence of this Tg value plus the amorphous nature of the polymer is that we have a material that is hard and transparent at room temperature. Isotactic polystyrenes have been known since 1955 but have not been of commercial importance. Syndiotactic polystyrene using metallocene catalysis has recently become of commercial interest. Both stereoregular polymers are crystalline with values of 230°C and 270°C for the isotactic and syndiotactic materials respectively. They are also somewhat brittle (see Section 16.3). 

In the crystalline region isotactic polystyrene molecules take a helical form with three monomer residues per turn and an identity period of 6.65 A. One hundred percent crystalline polymer has a density of 1.12 compared with 1.05 for amorphous polymer and is also translucent. The melting point of the polymer is as high as 230°C. Below the glass transition temperature of 97°C the polymer is rather brittle. 

The processing of blends of an amorphous material (polystyrene) and a crystalline material with a high melting point (PPO) reflects the nature of the constituent materials. The processing is mainly by injection moulding, and the major points to be considered when processing Noryl-type materials are ... 

An important subdivision within the thermoplastic group of materials is related to whether they have a crystalline (ordered) or an amorphous (random) structure. In practice, of course, it is not possible for a moulded plastic to have a completely crystalline structure due to the complex physical nature of the molecular chains (see Appendix A). Some plastics, such as polyethylene and nylon, can achieve a high degree of crystallinity but they are probably more accurately described as partially crystalline or semi-crystalline. Other plastics such as acrylic and polystyrene are always amorphous. The presence of crystallinity in those plastics capable of crystallising is very dependent on their thermal history and hence on the processing conditions used to produce the moulded article. In turn, the mechanical properties of the moulding are very sensitive to whether or not the plastic possesses crystallinity. 

Polyethylene has low density when polymerized at pressures 9,000 - 45,000 psi and high density when made with special catalysts at 250 - 500 psi. Low-density polyethylene softens 68 F lower than high-density polyethylene, which is more crystalline and stiffer. The rigidity characteristics and surface of high-density polyethylene are comparable with polystyrene. It feels like nylon, has a bursting strength three times that of low-density polyethylene, and withstands repeated exposure to 250 F, hence, it can be sterilized. 

Methylpentene polymer, a light plastic, has a crystalline melting point of 464 retention up to 392° F, transparency of 92%, and electrical properties similar to fluoroethylene. Its impact strength is greater than polystyrene and polymethyl methacr resistant to alkalies, weak acids, and non-chlorinated solvents. It may be injection m< implements for food packaging and preparation, medical care, and non-stick coating ... 

TPEs from blends of rubber and plastics constitute an important category of TPEs. These can be prepared either by the melt mixing of plastics and rubbers in an internal mixer or by solvent casting from a suitable solvent. The commonly used plastics and rubbers include polypropylene (PP), polyethylene (PE), polystyrene (PS), nylon, ethylene propylene diene monomer rubber (EPDM), natural rubber (NR), butyl rubber, nitrile rubber, etc. TPEs from blends of rubbers and plastics have certain typical advantages over the other TPEs. In this case, the required properties can easily be achieved by the proper selection of rubbers and plastics and by the proper change in their ratios. The overall performance of the resultant TPEs can be improved by changing the phase structure and crystallinity of plastics and also by the proper incorporation of suitable fillers, crosslinkers, and interfacial agents. 

These ideas might be used to explain the interesting results obtained recently by Williams et al.53 These workers observed formation of crystalline polystyrene when the reaction was initiated by triphenyl methyl potassium (or some other potassium metallo-organic compounds) in a hexane solution, but an amorphous polymer was formed in benzene. They point out that the catalyst is soluble in benzene but insoluble in hexane, and suggest that the heterogeneity of the catalyst is responsible for the results. Although this might be the case, an alternative explanation could be advanced.42 1... 

Typical crystalline plastics are polyethylene, polypropylene, nylon, acetals, and thermoplastic polyesters. Typical amorphous plastics are polystyrene, acrylics, PVC, SAN, and ABS. 

Figures 7-17 and 7-18 provides examples of modulus vs. Tg for amorphous and crystalline plastics. Temperature can help explain some of the differences observed in plastics. For example at room temperature polystyrene and acrylic are below their respective Tg values, we observe these materials in their glassy stage. In contrast, at room temperature natural rubber is above its Tg [Tg = —75°C (—103°F) Tm = 30°C(86°F)], with the result that it is very flexible. When it...

Dow ABS Nylon 6/6 Polycarbonate Polyethylene, HDPE, LDPE, LLDPE, ULDPE Polypropylene HPPP, CPPP Polystyrene HIPS, GPPS, Recycled, Advanced Styrenic Resin SAN Polyurethane Elastomers Polyolefin Plastomer PC/ABS Crystalline Polymer ABS/TPU... 

The Laboratory prepn for amorph styrene involves thermal conditions or the use of butyl-lithium at 50°. Crystalline polystyrene can be... 

It is typical, for instance, of syndiotactic polystyrene (s-PS) [7-9] and syndiotactic poly- p-methylstyrene (s-PPMS) [10] to present crystalline forms with a transplant conformation of the chains (shown for s-PS in Fig. 1) as well as crystalline forms with sequences of dihedral angles of the kind TTG+G+ (or the equivalent G G TT), corresponding to a s(2/l)2 helical symmetry of the chains (shown for s-PS in Fig. 1). 

A polymorphic behavior involving packing of chains having completely different conformations has been found also for isotactic polymers. For instance, isotactic polystyrene, under suitable experimental conditions, can produce crystalline gels in which the chains assume a nearly fully extended conformation [11,12], very close to a truns-planar, rather than the classical conformation of three-fold helix [13]. The two possible conformations proposed for the two crystalline forms of i-PS are shown in Fig. 2. 

Fig. 2 a, b. Side view and projection along the chain axis of models of isotactic polystyrene in the a) s(3/l) helical conformation b) nearly /raw-planar conformation, proposed for the crystalline gels [12]... 

Thin polymer films may also be investigated by TEM and high resolution images are obtained for e.g. thin films of liquid crystalline polymers [64]. Usually thin microtome cuts from bulk samples are investigated, but also epitaxial growth of polyoxymethylene on NaCl [152], chain folding of polyethylene crystals [153], epitaxial crystallization of polypropylene on polystyrene [154] or monomolecular polystyrene particles [155] are observed. The resolution is, however, in most cases not comparable to STM. 

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