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Crystalline Polymers Polyesters

We consider the case of the polymer -[(CH2)io-OOC-C6H4-OOC-C6H4 COO-C6H4-COO]n- (hereafter referred as HTH-10) whose phase transitions are the following K-S 221 °C S-I 260 °C. From the overall analysis of the temperature- [Pg.147]


Polymeric membranes are prepared from a variety of materials using several different production techniques. Table 5 summarizes a partial list of the various polymer materials used in the manufacture of cross-flow filters for both MF and UF applications. For microfiltration applications, typically symmetric membranes are used. Examples include polyethylene, polyvinylidene fluoride (PVDF) and polytetrafluoroethylene (PTFE) membrane. These can be produced by stretching, molding and sintering finegrained and partially crystalline polymers. Polyester and polycarbonate membranes are made using irradiation and etching processes and polymers such as polypropylene, polyamide, cellulose acetate and polysulfone membranes are produced by the phase inversion process.f Jf f ... [Pg.281]

LCP liquid crystalline polymer (polyester TBAB tetrabutylammonium bromide... [Pg.415]

D. M. Malik et al.. Characteristics of liquid crystalline polymer polyester polycarbonate blends, Polym. Engr. Set, 29 (4) 600 (1989). [Pg.357]

Figure 6.72 Chemical structures of monomers used to make liquid crystalline polymer polyesters. Figure 6.72 Chemical structures of monomers used to make liquid crystalline polymer polyesters.
Aromatic polyesters constitute an important class of main-chain liquid-crystalline polymers, but present the inconvenience of their reduced solubility and very high transition temperatures (sometimes not detected before the degradation of the sample). Their processability can be improved in several ways [2,3], e.g., reduction of the rigidity of the mesogen, lengthening of the spacer, or introduction of lateral substituents. [Pg.383]

Polyester, thermoplastic TP polyesters have different grades. Polybutylene tereph-thalate (PBT) a crystalline polymer and an excellent engineering material. It has marginal chemical resistance but resists moisture, creep, fire, fats, and oils. Molded items are hard, bright colored, and retain their impact strength at temperatures as low as — 40°F (-40°C). Uses include auto louvers, under-the-hood electricals, and mechanical parts. [Pg.428]

Aromatic polyesters that do not contain any flexible structural units are often nonmeltable or extremely high melting polymers that cannot be processed. Copolymerization is a way to obtain processable wholly aromatic polyesters The Tm versus copolyester composition curve is a U-shaped curve exhibiting a minimum that is generally well below the Tm of corresponding homopolymers. Liquid crystalline aromatic polyesters, for instance, are usually copolymers.72 An example is Ticona s Vectra, a random copolyester containing 4-oxybenzoyl and 6-oxy-2-naphthoyl units in ca. 70 30 mol ratio. This copolymer melts at ca. [Pg.35]

Liquid crystalline polymers (LCPs), 49 melt rheology of, 52 Liquid crystalline (LC) state, 48-49 Liquid crystalline thermotropic polyesters, 20... [Pg.588]

Macromolecules dendritic, 285 hyperbranched, 284-286 Main-chain liquid crystalline polymers, 49 Main-chain polyester LCP mesogenic units, 50... [Pg.588]

In order to make polymers behave as liquid crystals it is necessary to introduce some structural rigidity. A typical polymer which has the required rigidity is poly(phenylenetetraphthalamide) (10.7). This material belongs to a class of polymer known as the aramids. Other liquid crystalline polymers are the thermotropic polyesters derived from /7-hydroxybenzoic acid, p, p -biphenol and terephthalic acid (10.8). [Pg.157]

Although polymers in-service are required to be resistant toward hydrolysis and solar degradation, for polymer deformulation purposes hydrolysis is an asset. Highly crystalline materials such as compounded polyamides are difficult to extract. For such materials hydrolysis or other forms of chemolysis render additives accessible for analysis. Polymers, which may profitably be depolymerised into their monomers by hydrolysis include PET, PBT, PC, PU, PES, POM, PA and others. Hydrolysis occurs when moisture causes chain scissions to occur within the molecule. In polyesters, chain scissions take place at the ester linkages (R-CO-O-R ), which causes a reduction in molecular weight as well as in mechanical properties. Polyesters show their susceptibility to hydrolysis with dramatic shifts in molecular weight distribution. Apart from access to the additives fraction, hydrolysis also facilitates molecular characterisation of the polymer. In this context, it is noticed that condensation polymers (polyesters, -amides, -ethers, -carbonates, -urethanes) have also been studied much... [Pg.152]

Many industrial semi-crystalline polymer materials like polypropylene, polyamides, or polyesters contain nucleating agents or clarifiers which form needle-shaped aggregates already in the polymer melt. "For this purpose the pattern is desmeared using the measured primary beam. For a less involved treatment it may be sufficient to know the integral width of the primary beam profile in fiber direction. [Pg.180]

Liquid crystal phases, 15 100 Liquid-crystal polyesters (LCPs), 10 191-192 20 38-39 manufacture of, 20 44-45 Liquid-crystal polymers (LCPs), 15 110 20 3, 78-86, 398. See also Liquid crystalline polymers (LCPs) advantages of, 20 81... [Pg.526]

While no direct evidence of liquid crystallinity in PET-BB copolymers has been reported, the high-BB-content copolymers have been shown to possess morphologies similar to those of liquid crystalline polyesters [40], and show major changes in both melt relaxation times and fiber tensile moduli, suggestive of structural organization in a frustrated liquid crystalline polymer (LCP) (Table 6.3 and Figure 6.4) [41, 42],... [Pg.252]

The primary crystalline polymer based on CHDM is the terephthalate, poly(1,4-cyclohexylenedimethylene terephthalate) (PCT). This polyester was originally developed for fiber applications but has since found wider utility as a reinforced polymer for injection molding and (when copolymerized with a small amount of isophthalic acid) as a material for crystallized food packaging trays. The key property of PCT which sets it apart from other thermoplastic polyesters in these latter applications is its melting point. [Pg.273]

Liquid crystalline aromatic polyesters are a class of thermoplastic polymers that exhibit a highly ordered structure in both the melt and solid states. They can be used to replace such materials as metals, ceramics, composites and other plastics... [Pg.776]

The most relevant property of stereoregular polymers is their ability to crystallize. This fact became evident through the work of Natta and his school, as the result of the simultaneous development of new synthetic methods and of extensive stractural investigations. Previously, the presence of crystalline order had been ascertained only in a few natural polymers (cellulose, natural rubber, bal-ata, etc.) and in synthetic polymers devoid of stereogenic centers (polyethylene, polytetrafluoroethylene, polyamids, polyesters, etc.). After the pioneering work of Meyer and Mark (70), important theoretical and experimental contributions to the study of crystalline polymers were made by Bunn (159-161), who predicted the most probable chain conformation of linear polymers and determined the crystalline structure of several macromolecular compounds. [Pg.46]

Examples of crystalline polymers are nylons, cellulose, linear polyesters, and high-density polyethylene. Amorphous polymers are exemplified by poly(methyl methacrylate), polycarbonates, and low-density polyethylene. The student should think about why these structures promote more or less crystallinity in these examples. [Pg.281]

Crystalline polymers exhibit the following basic properties They are opaque as long as the size of the crystallites or spherulites, respectively, lies above the wavelength of light. Their solubility is restricted to few organic solvents at elevated temperature. The following crystalline polymers have attained technical importance as thermoplastic materials polyethylene, polypropylene, aliphatic polyamides, aliphatic/aromatic polyamides, aliphatic/aromatic polyesters, poly-oxymethylene, polytetrafluoroethylene, poly(phenylene sulfide), poly(arylene ether ketone)s. [Pg.28]

PET is a stiff crystalline polymer with a relatively high melting point. Aliphatic polyesters with more methylene groups than PET in the chain are more flexible and less crystalline than PET. [Pg.13]

Thermotropic liquid crystalline polymers, like polyesters containing mesogenic units on the main chain, may not be described by the wormlike chain model (cf. Sect. 1.2). The present article does not consider this type of polymers. [Pg.90]


See other pages where Crystalline Polymers Polyesters is mentioned: [Pg.279]    [Pg.147]    [Pg.11]    [Pg.442]    [Pg.279]    [Pg.147]    [Pg.11]    [Pg.442]    [Pg.293]    [Pg.299]    [Pg.306]    [Pg.185]    [Pg.261]    [Pg.26]    [Pg.71]    [Pg.47]    [Pg.233]    [Pg.134]    [Pg.467]    [Pg.119]    [Pg.246]    [Pg.15]    [Pg.271]    [Pg.222]    [Pg.80]    [Pg.293]    [Pg.299]    [Pg.300]    [Pg.306]    [Pg.349]   


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