Poly polyetherimide

AppHcation of an adhesion-promoting paint before metal spraying improves the coating. Color-coded paints, which indicate compatibiHty with specific plastics, can be appHed at 20 times the rate of grit blasting, typically at 0.025-mm dry film thickness. The main test and control method is cross-hatch adhesion. Among the most common plastics coated with such paints are polycarbonate, poly(phenylene ether), polystyrene, ABS, poly(vinyl chloride), polyethylene, polyester, and polyetherimide. 

Polymerization of the dianhydride and diamine proceeds through an intermediate poly(amide acid) stage before ring closure converts the adjacent acid and amide groups to the polyetherimide (94). The polymerization can be carried directiy to the polyetherimide as a single-step process, or first to an ainide—acid-containing prepolymer, which can be isolated, and then to the polyetherimide. 

Some of the common types of plastics that ate used ate thermoplastics, such as poly(phenylene sulfide) (PPS) (see Polymers containing sulfur), nylons, Hquid crystal polymer (LCP), the polyesters (qv) such as polyesters that ate 30% glass-fiber reinforced, and poly(ethylene terephthalate) (PET), and polyetherimide (PEI) and thermosets such as diaHyl phthalate and phenoHc resins (qv). Because of the wide variety of manufacturing processes and usage requirements, these materials ate available in several variations which have a range of physical properties. 

The PEEK resia is marketed as aeat or filled pellets for iajectioa mol ding, as powder for coatiags, or as preimpregaated fiber sheet and tapes. Apphcations iaclude parts that are exposed to high temperature, radiation, or aggressive chemical environments. Aerospace and military uses are prominent. At present, polyamideimide (PAl) resia and poly(arylene sulfides) are the main competitors for apphcations requiring service temperatures of 280°C. At lower temperatures, polyethersulfones, amorphous nylons, and polyetherimides (PEI) can be considered. 

PEI homopolyesters. See Poly(ethylene isophthalate) (PEI) homopolyesters PEIs. See Polyetherimides (PEIs)... 

Notes-. PES, poly(aryl ether sulphone) PEEK, poly(aryl ether ether ketone) PC, polycarbonate PEI, polyetherimide PPS, poly(phenylene sulphide). 

Polyetherimide-polysiloxane multiblock copolymers, 24 716 Polyetherimides (PEI), 10 217—218 Polyether impression materials, 8 332-333 Poly(ether ketones) (PEK), 10 197-199 Polyether polyols, 25 455-456,464,468t, 470 propylene oxide polymerization to, 20 793-794, 812 Poly ethers, 12 663... 

Property Test Method Units PEN Polyimide Polyetherimide Poly(ethylene terephthalate) film Polypropylene sulfide)... 

Glassy polymers with much higher glass transition temperatures and more rigid polymer chains than rubbery polymers have been extensively used as the continuous polymer matrices in the zeolite/polymer mixed-matrix membranes. Typical glassy polymers in the mixed-matrix membranes include cellulose acetate, polysul-fone, polyethersulfone, polyimides, polyetherimides, polyvinyl alcohol, Nafion , poly(4-methyl-2-pentyne), etc. 

DMTA is a very interesting tool for characterizing heterogeneous materials in which domains of distinct Tg values coexist. The most interesting cases involve modified thermosets of different types (see Chapter 8). Examples are the use of rubbers (e.g., liquid polybutadiene and random copolymers), or thermoplastics (e.g., polyethersulphone or polyetherimide in epoxy matrices or poly(vinyl acetate) in unsaturated polyesters), as impact modifier (epoxies), or low-profile additives (polyesters). The modifier-rich phase may be characterized by the presence of a new a peak (Fig. 11.10). But on occasions there may be superposition of peaks and the presence of the modifier cannot be easily detected by these techniques. If part of the added polymer is soluble in the thermoset matrix, its eventual plasticizing effect can be determined from the corresponding matrix Tg depletion, and the... 

Many computational studies of the permeation of small gas molecules through polymers have appeared, which were designed to analyze, on an atomic scale, diffusion mechanisms or to calculate the diffusion coefficient and the solubility parameters. Most of these studies have dealt with flexible polymer chains of relatively simple structure such as polyethylene, polypropylene, and poly-(isobutylene) [49,50,51,52,53], There are, however, a few reports on polymers consisting of stiff chains. For example, Mooney and MacElroy [54] studied the diffusion of small molecules in semicrystalline aromatic polymers and Cuthbert et al. [55] have calculated the Henry s law constant for a number of small molecules in polystyrene and studied the effect of box size on the calculated Henry s law constants. Most of these reports are limited to the calculation of solubility coefficients at a single temperature and in the zero-pressure limit. However, there are few reports on the calculation of solubilities at higher pressures, for example the reports by de Pablo et al. [56] on the calculation of solubilities of alkanes in polyethylene, by Abu-Shargh [53] on the calculation of solubility of propene in polypropylene, and by Lim et al. [47] on the sorption of methane and carbon dioxide in amorphous polyetherimide. In the former two cases, the authors have used Gibbs ensemble Monte Carlo method [41,57] to do the calculations, and in the latter case, the authors have used an equation-of-state method to describe the gas phase. 

Specialty polymers achieve very high performance and find limited but critical use in aerospace composites, in electronic industries, as membranes for gas and liquid separations, as fire-retardant textile fabrics for firefighters and race-car drivers, and for biomedical applications (as sutures and surgical implants). The most important class of specialty plastics is polyimides. Other specialty polymers include polyetherimide, poly(amide-imide), polybismaleimides, ionic polymers, polyphosphazenes, poly(aryl ether ketones), polyarylates and related aromatic polyesters, and ultrahigh-molecular-weight polyethylene (Fig. 14.9). 

According to literary data, the following mixtures of aromatic/aliphatic-aromatic hydrocarbons were separated toluene/ n-hexane, toluene/n-heptane, toluene/n-octane, toluene/f-octane, benzene/w-hexane, benzene/w-heptane, benzene/toluene, and styrene/ethylbenzene [10,82,83,109-129]. As membrane media, various polymers were used polyetherurethane, poly-esterurethane, polyetherimide, sulfonyl-containing polyimide, ionicaUy cross-linked copolymers of methyl, ethyl, n-butyl acrylate with acrilic acid. For example, when a composite polyetherimide-based membrane was used to separate a toluene (50 wt%)/n-octane mixture, the flux Q of 10 kg pm/m h and the separation factor of 70 were achieved [121]. When a composite mebrane based on sulfonyl-containing polyimide was used to separate a toluene (1 wt%)/ -octane mixture, the flux 2 of 1.1 kg pm/m h and the separation factor of 155 were achieved [10]. When a composite membrane based on ionically cross-linked copolymers of methyl, ethyl, w-butyl acrylate with acrilic acid was used to separate toluene (50 wt%)//-octane mixture, the flux Q of 20-1000 kg pm/m h and the separation factor of 2.5-13 were achieved [126,127]. 

Poly(dimethylsiloxane-co-oxyethylene-co-oxypropylene) is used as a surfactant, dispersant, and wetting agent, while poly[bisphenol A bis(oxyranylmethyl) ether]-co-poly(dimethylsiloxane) is used as an epoxy resin. More complicated silicone copolymers also were synthesized such as the silicone polyetherimide shown below ... 

This copolymer can be obtained from a polydimethylsiloxane that has aminoalkyl end groups in a reaction with the polyetherimide formed from the reaction of a bis(ether anhydride) with diaminobenzene. The material is fire resistant and is used in cable insulations. Among other more complex copolymers with practical applications are poly[2,2-propanebis(4-phenyl)-carbonate]-b/ock-poly(dimethylsiloxane)] and a silicone phenol formaldehyde copolymer obtained in two steps, the first being the heating of a polydimethylsiloxane that has reactive end groups with glycerol, and the second step being the reaction with a phenol formaldehyde resin. 

Among these processes, only the Hock process and the toluene oxidation are important industrially. The other processes were discarded for economic reasons. In the Hock process acetone is formed as a by-product. This has not, however, hindered the expansion of this process, because there is a market for acetone. New plants predominantly use the cumene process. More than 95% of the 4,691,000 my (m = metric tonnes) consumed is produced by the cumene peroxidation process. Phenol s consumption growth rate of 3% is primarily based on its use in engineering plastics such as polycarbonates, polyetherimide and poly(phenylene oxide), and epoxy resins for the electronic industry. The Mitsui Company is, for instance, the world s second largest producer of phenol. Japan s production... 

Typical UF membrane materials are polysulfone (PS), poly ether sulfone (PES), polyetheretherketone (PEEK), cellulose acetate (CA), polyacrylonitrile (PAN), polyvinylidene fluoride (PVDF), polyimide (PI), and polyetherimide (PEI) ... 

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