Polymers hydroquinone

A typical example of a small liquid crystalline molecule, derived from terephthalic acid and the ethyl ether of hydroquinone, has a liquid crystalline range between 215 and 267 C. However, the liquid crystalline polymer, hydroquinone terephthalate, is so high melting (above 600°C) that it decomposes before exhibiting a transition from the crystalline to the liquid crystalline state.1... 

The polymeric products can be made to vary widely in physical properties through controlled variation in the ratios of monomers employed in thek preparation, cross-linking, and control of molecular weight. They share common quaHties of high resistance to chemical and environmental attack, excellent clarity, and attractive strength properties (see Acrylic ester polymers). In addition to acryHc acid itself, methyl, ethyl, butyl, isobutyl, and 2-ethylhexyl acrylates are manufactured on a large scale and are available in better than 98—99% purity (4). They usually contain 10—200 ppm of hydroquinone monomethyl ether as polymerization inhibitor. 

Acryhc acid and esters are stabilized with minimum amounts of inhibitors consistent with stabihty and safety. The acryhc monomers must be stable and there should be no polymer formation for prolonged periods with normal storage and shipping (4,106). The monomethyl ether of hydroquinone (MEHQ) is frequentiy used as inhibitor and low inhibitor grades of the acrylate monomers are available for bulk handling. MEHQ at 10—15 ppm is generally... 

Another commercial appHcation of nucleophilic reactions of nitro-free duoroaromatics is the manufacture of polyetheretherketone (PEEK) high performance polymers from 4,4 -diduoroben2ophenone [345-92-6], and hydroquinone [121-31-9] (131) (see PoLYETHERS, AROMATIC). 

Phthahc resins are usually processed to an acid number of 25—35, yielding a polymer with an average of 1800—2000. The solution viscosity of the polymer is usually followed to ascertain the polymer end point. The resin is cooled to 150°C and hydroquinone stabilizer (150 ppm) is added to prevent premature gelation during the subsequent blending process with styrene at 80°C. The final polymer solution is cooled to 25°C before a final quaUty check and dmmming out for shipment. 

The original recipe adopted by the U.S. Government Synthetic Rubber Program was known as the "Mutual Recipe" and is shown iu Table 4. As can be seen, the reaction temperature was set at 50°C, which resulted iu 75% conversion to polymer iu about 12 h. The reaction was then stopped by addition of a "shortstop," such as 0.1 parts hydroquinone, which destroyed any residual catalyst (persulfate), and generated quiuone, which helped inhibit any further polymerisation. 

Propionaldehyde [123-38-6] M 58.1, b 48.5-48.7 , d 0.804, n 1.3733, n S 1.37115. Dried with CaS04 or CaCl2, and fractionally distd under nitrogen or in the presence of a trace of hydroquinone (to retard oxidation). Blacet and Pitts [J Am Chem Soc 74 3382 1952] repeatedly vacuum distd the middle fraction until no longer gave a solid polymer when cooled to -80°. It was stored with CaS04. 

Polycarbonates were first prepared by Einhom in 1898 by reacting the dihydroxybenzenes, hydroquinone and resorcinol, separately with phosgene in solution in pyridine. The hydroquinone polycarbonate was an infusible and insoluble crystalline power whereas the resorcinol polymer was an amorphous material melting at about 200°C. The third dihydroxybenzene, catechol, yields a cyclic carbonate only, which is not surprising bearing in mind the proximity of... 

Hydroquinone polyesters Soluble polymers with melting points of 335°C (635°F) to over 400° C (752°F). 

However, many salts such as the hydroquinone or biphenol salt are so insoluble diat they do not work well by this procedure. Furthermore, a stoichiometric amount of base used for die reaction is critical to obtain high-molecular-weight polymers. Moreover, die sd ong base may undesirably hydrolyze the dihalides to afford deactivated diphenolates, which upset the stoichiometry. Clendining et al. reported that potassium carbonate or bicarbonate could be used in these reactions instead of corresponding hydroxides.60 McGrath and co-workers were the first to systematically study die use of the weak base K2C03 instead of a strong base to obtain phenolate salts.8,61,62 Potassium carbonate was found to be better than... 

Other polymers have been reported from the reactions of N3P3CI6 with alkoxyboron compounds, the sodium salt of hydroquinone, and 4,4 -dihydroxybiphenyl. ... 

Providing an ion exchanger with a sufficient number of redox groups so that conduction can occur by a relay-type redox-change mechanism. Examples are hydroquinone-derived redox polymers and polyvinyl polymers with a tetrathia-fulvalene, ferrocene, or carbazole group, which have been found useful for research and analytical applications. 

Shindo H, Huang PM (1985a) The catalytic power of inorganic components in the abiotic synthesis of hydroquinone-derived humic polymers. Appl Clay Sci 1 71-81... 

Wang MC, Huang PM (1986) Humic macromolecular interlayering in nontronite through interaction with phenol monomers. Nature (London) 323 529-531 Wang MC, Huang PM (1988) Catalytic power of nontronite, kaolinite, and quartz and their reaction sites in the formation of hydroquinone-derived polymers. Appl Clay Sci 4 43-57... 

X-ray diffraction measurements have shown that Bisphenol-AF-derived poly(aryloxydiphenylsilane) is amorphous.28 The Tg value of 106°C is higher than that of the poly(aryloxydiphenylsilane)s derived from dianilinodiphenylsilane and bisphenols such as 4,4 -biphenol, 2,7-dihydroxynaphthalene, and hydroqui-none.28 The aromatic units in poly(aryloxy-diphenylsilane(s) have a remarkable effect on the Tg. The thermal stability of this polymer is somewhat lower than those of poly(aryloxydiphenylsilane)s derived from dianilinodiphenylsilane and bisphenols such as 4,4 -biphenol, 2,7-dihydroxynaphthalene, and hydroquinone. The DT10 is 362°C and the residual weight at 500°C in air is 54%. 

Phenols, quinones and aromatic amines reduce the rate of polymerisation by reacting with polymer radical. They lose a hydrogen readily but resultant radicals are not initiators. Inhibitors are added to monomers to prevent polymerisation during storage. Hydroquinone and t-butylcatechol in 0.001 to 0.1 per cent concentration act as inhibitors. 

Hydroquinone, nitrobenzene, dinitrobezene and benzothiazine are generally used as inhibitors in polymer industry. The inhibiting action of these can be shown as follows ... 

Polycarbonates are polyesters of phenols and carbonic acid. Polycarbonates are polymer containing O CO O groups. They were prepared accidentally in 1989 by Einhom by the action of phosgene with hydroquinone. He also prepared a resin by reacting phosgene with resorcinol. Bischoff and Hedenstrom in 1902 reacted dihydricphenols with diphenylcarbonate to get insoluble materials. Carothers and others prepared aliphatic Polycarbonates in 1930 but they were of no commercial importance. 

The polymers used in this study were prepared by a nucleophilic activated aromatic substitution reaction of a bisphenate and dihalo diphenyl sulfone ( ). The reaction was carried out in an aprotic dipolar solvent (NMP) at 170°C in the presence of potassium carbonate (Scheme 1) (5,6). The polymers were purified by repeated precipitation into methanol/water, followed by drying to constant weight. The bisphenols used were bisphenol-A (Bis-A), hydroquinone (Hq) and biphenol (Bp). Thus, the aliphatic character of Bis-A could be removed while retaining a similar aromatic content and structure. The use of biphenol allows an investigation of the possible effect of extended conjugation on the radiation degradation. 

Polymers and resins Water purification, including removal of phenol, chlorophenols, ketones, alcohols, aromatics, aniline, indene, polynuclear aromatics, nitro- and chlor-aromatics, PCB, pesticides, antibiotics, detergents, emulsifiers, wetting agents, kraftmill effluents, dyestuffs recovery and purification of steroids, amino acids and polypeptides separation of fatty adds from water and toluene separation of aromatics from ahphatics separation of hydroquinone from monomers recovery of proteins and enzymes removal of colours from symps ... 

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