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Monomers polyimide

Imide-based polymers, 10 8 Imide-containing monomers, polyimide synthesis using, 20 272 Imide ring formation, polyimide synthesis via, 20 265 Imides... [Pg.464]

During polycondensation of salt monomers, polyimides were obtained from salts of aliphatic diamines and pyromellitic acid or its diethyl ester in the presence of a small amount of a polar organic medium (Figure 45). ... [Pg.1007]

VDP Polyimides. Polyimide films have also been prepared by a kind of VDP (16). The poly(amic acid) layer is first formed by the coevaporation and condensation of two monomers, followed by copolymerization on the substrate. The imidization is carried out in a separate baking step (see POLYIMIDES). [Pg.430]

Since successful commercialization of Kapton by Du Pont Company in the 1960s (10), numerous compositions of polyimide and various new methods of syntheses have been described in the Hterature (1—5). A successful result for each method depends on the nature of the chemical components involved in the system, including monomers, intermediates, solvents, and the polyimide products, as well as on physical conditions during the synthesis. Properties such as monomer reactivity and solubiHty, and the glass-transition temperature,T, crystallinity, T, and melt viscosity of the polyimide products ultimately determine the effectiveness of each process. Accordingly, proper selection of synthetic method is often critical for preparation of polyimides of a given chemical composition. [Pg.396]

Bis-maleimide resins composed of BMI and diamines have been reported in the early 1960s in the patent literature. Since that time, a number of patents have appeared describing improvements in their properties and uses [3]. Although many bis-maleimide resins are commercially developed, relatively few reports of their use as adhesives are to be found in scientific journals [4-10]. Improvements of maleimide resins are mirrored in the improvements of thermosetting polyimides. For example, the method of in situ polymerization of monomer reactants (PMR method) was developed [6]. [Pg.814]

The utilization of N-silylated diamines as polyamide and polyimide forming monomers has recently been exhaustively reported by Kakimoto et al. [105] and Oishi et al. [106]. But their work is beyond the scope of this... [Pg.45]

Basically, the first approach to correlate the polyimide chain organization to the monomer structure was to take into consideration the electron affinity of the anhydride and the ionization potential of the diamine,10 as shown in Fig. 5.3. The strongest interactions between the polymeric chain are expected when the polyimide is prepared with the dianhydride having the highest electron affinity and die diamine with the lowest ionization potential. The strongest interchain interaction leads to high Tg and low solubility. [Pg.274]

Figure 5.7 Fluorinated monomers used for preparation of colorless polyimides. Figure 5.7 Fluorinated monomers used for preparation of colorless polyimides.
Figure 5.11 Monomers for preparation of rodlike polyimides with low coefficient of thermal expansion. Figure 5.11 Monomers for preparation of rodlike polyimides with low coefficient of thermal expansion.
The first patent of Edwards and Robinson147 claims the condensations of pyromel-litic acid and aliphatic diamine salt to prepare polyimide. Recently, that approach has been revisited, and biphenyl tetracarboxylic and pyromellitic acids give a salt monomer by reaction with 1 mol of an aliphatic diamine (octamethylene diamine and dodecamethylene diamine). The salts were polymerized under 250 MPa at 250°C for 5 h in closed reaction vessels (Fig. 5.32) giving crystalline polymers.148 By reaction of pyromellitic tetraacid with oxydianiline, it has been possible to isolate a monomeric salt. It was polymerized under 30 MPa giving a PMDA-ODA polyimide with water elimination. [Pg.303]

An unusual method has been used to prepare a hyperbranched polyimide starting from two monomers a difunctional A2 and a trifunctional B3. The gel formation can be avoided with careful control of the polycondensation conditions (molar ratio, order of the monomer addition, and low concentration). The A2 and B3 monomers were respectively 6FDA and tris(4-aminophenyl)... [Pg.308]

AABB polyimides, synthesis of, 300-302 AA-BB-type polymers, 135 AA-BB-type sulfonylation, 330 AA monomers, 11-12 A-B-A triblock copolymers, 7 A-B copolymers, 7 AxBy monomers, 8 AB polyamides, 173-180 AB polyimides, 304-307 syntheses of, 306 Abrasion resistance test, 243-244 ABS. See Acrylonitrile-... [Pg.575]

Biaryl derivatives bearing reactive groups have become increasingly important in industry. Uses for this class of compounds are constantly being developed in the production of high performance polymers. Materials such as 3,3, 4,4 -biphenyl-tetracarboxylic dianhydride 1 and 4,4 -biphenol 2 are monomers employed in the manufacture of high performance polyimides or polyesters. Applications for this family of molecules have also been found both in the dye industry and in the pharmaceutical industry. [Pg.217]

Jmai", Y.i Rapid Synthesis of Polyimides from Nylon-Salt Monomers. Vol. 140, pp. 1-23. [Pg.210]

The monomer synthesis and cyclopolymerization were carried out following the procedure of Butler et al. (21). The resulting polyimide was shown to possess primarily pyrrolidine rings as indicated by infrared spectroscopy (21). Initially, the reduction was carried out with LiAlH in tetrahydrofuran. [Pg.78]

Polyimide matrix materials, 26 763-764 Polyimide powders, 20 284 Polyimide synthesis, 20 264-276 using imide-containing monomers, 20 272... [Pg.732]

There continue to be a few examples reported where rearrangement has been used synthetically to develop new products sometimes important in the industrial world. Monomers for polyamides and polyimides (which are used for making moisture sensitive films, fibres and mouldings) have been synthesized24 by the reduction of a nitro compound, followed by a benzidine rearrangement of the resulting hydrazobenzene derivative as outlined in Scheme 5. [Pg.863]

Einsla, B. R., Hong, Y. T., Kim, Y. S., Wang, F., Gunduz, N. and McGrath, J. E. 2004. Sulfonated naphthalene dianhydride based polyimide copolymers for proton-exchange-membrane fuel cells. 1. Monomer and copolymer synthesis. Journal of Polymer Science Part A Polymer Chemistry 42 862-874. [Pg.180]


See other pages where Monomers polyimide is mentioned: [Pg.233]    [Pg.233]    [Pg.400]    [Pg.401]    [Pg.406]    [Pg.7]    [Pg.49]    [Pg.819]    [Pg.46]    [Pg.293]    [Pg.295]    [Pg.300]    [Pg.303]    [Pg.307]    [Pg.589]    [Pg.60]    [Pg.873]    [Pg.2]    [Pg.99]    [Pg.155]    [Pg.459]    [Pg.126]    [Pg.107]    [Pg.36]    [Pg.102]    [Pg.601]    [Pg.246]    [Pg.664]    [Pg.336]    [Pg.16]    [Pg.22]   
See also in sourсe #XX -- [ Pg.96 ]




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