Poly sulfonic diphenyl

Dichloro- Poly(arylene diphenyl ether sulfone)... 

Noshay and Robeson27 reviewed the extensive patent literature on poly(sulfonated aromatics) and their industrial applications. They carried out the sulfonation of a bisphenol-diphenyl sulfone polycondensate by means of a 2 1 S03/TEP complex38 in... 

Z.S. Mai, H.M. Zhang, X.R Li, C. Bi and H. Dai, Sulfonated poly (tetramethy-diphenyl ether ether ketone) membranes for vanadium redox flow battery application,. Power Sources 196,2011,482-487. 

Sulfonation has been used to change some characteristics of blends. Poly(2,6-diphenyl-l,4-phenylene oxide) and polystyrene are immiscible. However, when the polymers were functionalized by sulfonation, even though they remained immiscible when blended, the functionalization increased interfacial interactions and resulted in improved properties (65). In the case of DMPPO and poly(ethyl acrylate) the originally immiscible blends showed increased miscibility with sulfonation (66). 

Polyarylether Ketones. The aromatic polyether ketones are tme thermoplastics. Although several are commercially available, two resins in particular, poly ether ether ketone [31694-16-3] (PEEK) from ICI and poly ether ketone ketone (PEKK) from Du Pont, have received most of the attention. PEEK was first synthesized in 1981 (20) and has been well studied it is the subject of numerous papers because of its potential use in high performance aircraft. Tough, semicrystalline PEEK is prepared by the condensation of bis(4-fiuorophenyl) ketone with the potassium salt of bis(4-hydroxyphenyl) ketone in a diaryl sulfone solvent, such as diphenyl sulfone. The choice of solvent is critical other solvents, such as Hquid HE, promote the reaction but lead to premature low molecular-weight crystals, which do not exhibit sufficient toughness (21). 

Recently, the pyrazole group containing bisphenols have been synthesized from activated aromatic dihalides and 3,5-bis (4-hydroxy phenyl)-4-phenyl pyrazole or 3,5-bis(4-hydroxy phenyl)-1,4-diphenyl pyrazole. A novel synthesis of imido aryl containing bisphenols has been reported [32]. N-substituted l,4-bis(4-hydroxy phenyl)-2,3-naphthalimides were prepared from phenolphthalein and copolymerized with aromatic sulfone or ketone difluorides to obtain the poly(imidoaryl ether) sulfones/ ketones. 

Polysulfonation of self-polycondensation of 4-(phenylthio)benzenesulfonyl chloride was also used to prepare poly(arylene sulfide sulfone)s.245,246 Condensation of diphenyl sulfide with d -oxydibenzenesulfonic acid or d.d -thiodibcn/cnc-sulfonic acid247 or by poly etherification of poly condensation of DC DPS with d.d -dihydroxydiphenol sulfide occurred.5... 

Diphenyl sulfone (DPS), 338 Diphenyl terephthalate-diphenyl isophthalate-bisphenol-A melt poly esterification, 111-112 Direct polyesterification, 63-69 Distinctness of image (DOI), 245 Divergent method, 8... 

The molecular weights of poly(ketone)s obtained from diphenyl ketone and diphenyl sulfone are lower than those from diphenyl ether and diphenyl sulfide. The former monomers possess highly electron-withdrawing carbonyl or sulfone groups, which lower the electron density of the rings. 

The poly(arylene ether sulfones) comprise strictly alternating bisphenol and diphenyl sulfone units. Similarly, "copolymers" were prepared using two different bisphenols, which produced a statistical sequence with the alternating diphenyl sulfone units. 

Xing, P., Robertson, G. R, Guiver, M. D., Mikhailenko, S. D. and Kaliaguine, S. 2004. Sulfonated poly(aryl ether ketone)s containing the hexafluoroisopro-pylidene diphenyl moiety prepared by direct copolymerization, as proton exchange membranes for fuel cell application. Macromolecules 37 7960-7967. 

Poly(aryl ether ketone) Cone, sulfuric acid, trifluorometh-anesulfonic acid, diphenyl sulfone, sulfolane Alcohol, ether, methylene chloride... 

Poly(phenylene sulfide) Above 200 °C dichlorobiphenyl, 1-chlo ronaphthalene, W-ethylpyrrolidone, -caprolactam, diphenyl ether, diphenyl sulfone ... 

Poly(arylene ether benzoxazole)s were also synthesized from the reaction of bis[(4-hydroxyphenyl)benzoxazole]s and activated aromatic difluoro monomers as shown in Eq. (7) [28,29]. The bis[(4-hydroxyphenyl)benzoxazole]s were readily prepared by condensation of the appropriate bis(o-aminophenol) (e.g. 3,3 -dihydroxy-4,4 -diaminobiphenyl) with phenyl-4-hydroxybenzoate in diphenyl sulfone at 260°C. Under proper conditions, the less expensive 4-hydroxybenzoic acid can be used in place of the phenyl ester to provide high yields of the desired bis[(4-hydroxyphenyl)benzoxazole]s. As presented in Table 9, the hexafluoroisopropylidene (6F) containing polymers were amorphous. These polymers were prepared in DMAc. However, the polymers derived from 6,6 -bis[2-(4-hydroxyphenyl)benzoxazole] were prepared in diphenyl sul-... 

Poly(arylene ether benzimidazole)s have received more attention than any other PAE containing heterocyclic units. This is due primarily to their unique combination of properties even at relatively low molecular weights and their potential for use in several high performance applications. The initial report in 1991 involved polymers from the reaction of 3 different bis[(4-hydroxy-phenyl)benzimidazole]s with various activated aromatic difluoro monomers as shown in Eq. (10) [37]. The bis[(4-hydroxyphenyl)benzimidazole]s were prepared from the reaction of aromatic bis(o-diamines) and phenyl-4-hydroxybenzoate in diphenyl sulfone. The use of 4-hydroxybenzoic acid would obviously reduce the... 

Figure 8.12 TEM photographs of triblock copolymers dispersed in a DGEBA-diamine epoxy network. The triblock copolymer is polystyrene-b-polybuta-diene-b-poly(methyl methacrylate), and the epoxy hardener is (a) -methylene bis [3-chloro-2,6 diethylaniline], MCDEA, and (b) 4,4 -diamino diphenyl sulfone, DDS. In the case of the epoxy system based on MCDEA, the PMMA block is miscible up to the end of the epoxy reaction. In the case of the epoxy system based on DDS, the PMMA block phase-separates during reaction. (From LMM Library.)... 

PB PBI PBMA PBO PBT(H) PBTP PC PCHMA PCTFE PDAP PDMS PE PEHD PELD PEMD PEC PEEK PEG PEI PEK PEN PEO PES PET PF PI PIB PMA PMMA PMI PMP POB POM PP PPE PPP PPPE PPQ PPS PPSU PS PSU PTFE PTMT PU PUR Poly(n.butylene) Poly(benzimidazole) Poly(n.butyl methacrylate) Poly(benzoxazole) Poly(benzthiazole) Poly(butylene glycol terephthalate) Polycarbonate Poly(cyclohexyl methacrylate) Poly(chloro-trifluoro ethylene) Poly(diallyl phthalate) Poly(dimethyl siloxane) Polyethylene High density polyethylene Low density polyethylene Medium density polyethylene Chlorinated polyethylene Poly-ether-ether ketone poly(ethylene glycol) Poly-ether-imide Poly-ether ketone Poly(ethylene-2,6-naphthalene dicarboxylate) Poly(ethylene oxide) Poly-ether sulfone Poly(ethylene terephthalate) Phenol formaldehyde resin Polyimide Polyisobutylene Poly(methyl acrylate) Poly(methyl methacrylate) Poly(methacryl imide) Poly(methylpentene) Poly(hydroxy-benzoate) Polyoxymethylene = polyacetal = polyformaldehyde Polypropylene Poly (2,6-dimethyl-l,4-phenylene ether) = Poly(phenylene oxide) Polyp araphenylene Poly(2,6-diphenyl-l,4-phenylene ether) Poly(phenyl quinoxaline) Polyphenylene sulfide, polysulfide Polyphenylene sulfone Polystyrene Polysulfone Poly(tetrafluoroethylene) Poly(tetramethylene terephthalate) Polyurethane Polyurethane rubber... 

Figure 4.46. Molecular structures of commonly used OLED/PLED materials. Shown are (a) Alq3 (tris(quinoxalinato)Al (III)) used as an electron-transport material (b) DIQA (diisoamylquinacridone) used as an emissive dopant (c) BCP (2,9-dimethyl-4,7-diphenyl-l,10-phenanthroline) used as an exciton/ hole blocking agent (d) NPB (l,4-bis(l-napthylphenyl amino)biphenyl) (e) PFO (9,9-dioctylfluorene) used as an emissive polymer in PLEDs (f) PEDOT-PSS (poly-3,4-ethylenedioxythiophene-polystyrene sulfonate) used as a hole transport material in PLEDs.

Ballard Advanced Materials (BAM) ionomers are sulfonated copolymers of trifluorostyrene and substimted trifluorostyrene monomers. BAM, a subsidiary of Ballard Power Systems, investigated the conducting polymers based on polyphenylquinoxaline (PPQ). These can be sulfonated in a wide range and were referred to as BAMIG (Ballard first generation) membranes, but these membranes were found to have short durability. To overcome this problem, BAM developed a second generation of advanced membranes based on two distinct material types. The first material type consisted of a series of sulfonated poly(2,6-diphenyl 1,4-phenylene oxide). The second material type consisted of a series of sulfonated poly(arylether sulfone). But the durability of these membranes was also insufficient. Since the durability of previous membranes was limited, Ballard produced a novel family of sulfonated membranes based on a,p,p-ttifluorostyrene monomers and a series of substituted ttifluoro-comonomers... 

FIGURE 1.2. Molecular structure of widely used it-conjugated and other polymers (a) poly(para-phenylene vinylene) (PPV) (b) a (solid line along backbone) and it ( clouds above and below the a line) electron probability densities in PPV (c) poly(2-methoxy-5-(2 -ethyl)-hexoxy-l,4-phenylene vinylene) (MEH-PPV) (d) polyaniline (PANI) (d.l) leucoemeraldine base (LEB), (d.2) emeraldine base (EB), (d.3) pernigraniline base (PNB) (e) poly(3,4-ethylene dioxy-2,4-thiophene)-polystyrene sulfonate (PEDOT-PSS) (f) poly(IV-vinyl carbazole) (PVK) (g) poly(methyl methacrylate) (PMMA) (h) methyl-bridged ladder-type poly(jf-phenylene) (m-LPPP) (i) poly(3-alkyl thiophenes) (P3ATs) (j) polyfluorenes (PFOs) (k) diphenyl-substituted frares -polyacetylenes (f-(CH)x) or poly (diphenyl acetylene) (PDPA). 

PAN, Epoxy I, DGEBA (diglycyl ether of bisphenol A) epoxy resin with 35% w/w of diamino diphenyl sulfone hardener, T300, polyacrylonitrile (PAN)-based C fiber PTEDM, poly(2,2 -thiobisethanol dimethacrylate) PNDM, poly(W-methyldiethanolamine dimethacrylate). Oxyfiuorination is a proprietary treatment of Air Products and Chemicals that results in surface oxidation and fiuorination of fibers. 

Poly(biphenyl ether sulfone)s with improved polydispersity, a lower level of undesirable low-molecular-weight oligomeric components and improved melt flow properties have 4,4 -biphenylene, p-phenylene, 4,4 -di-phenyl sulfone and 2,2-diphenyl propane groups in the backbone. ... 

SYNTHESIS Condensation polymerization of 3,3, 4,4 -tetraaminobiphenyl (TAB) and diphenyl isophthalate (DPIP) in poly(phosphoric) acid, or in a hot molten nonsolvent such as sulfolane or diphenyl sulfone. ... 

Tsuchida et al. [95,96] reported the synthesis of poly(thiophenylene sulfonic acid) containing up to two sulfonic acid groups per repeating unit. Polymerisation of 4-(methylsulfinyl)diphenyl sulfide in sulfuric add upon heating or in the presence of SO3 resulted in sulfonated poly(sulfonium cation), which was then converted into the corresponding sulfonated poly(phenylene sulfide). 

---