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Polycarbonate yield

The d adation products of polyesters in alkali fusion are polyols and polybasic carboxylic acids polycarbonates yield also diphenols. The optimum reaction temperatures vary and are compiled in Table 17. [Pg.62]

Fig. 2. Stress—strain curve for standard polycarbonate resin at 23°C where the points A, B, and C correspond to the proportional limit (27.6 MPa), the yield point (62 MPa), and the ultimate strength (65.5 MPa), respectively. To convert MPa to psi, multiply by 145. Fig. 2. Stress—strain curve for standard polycarbonate resin at 23°C where the points A, B, and C correspond to the proportional limit (27.6 MPa), the yield point (62 MPa), and the ultimate strength (65.5 MPa), respectively. To convert MPa to psi, multiply by 145.
When the catalyst is triethylamine, the yield is nearly 100% cycHc oligomers but if pyridine is used, the polymer is nearly 100% linear. A basic catalyst in the second step, such as lithium stearate or an organic titanate [bis-(acetylacetonato)diisopropoxytitanium], produces a polycarbonate with a molecular weight of 250,000—300,000 when polymerized at 300°C for 30 min. A fiber glass composite has been prepared using this basic procedure (39). [Pg.42]

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... [Pg.556]

Crystallisable polymers have also been prepared from diphenylol compounds containing sulphur or oxygen atoms or both between the aromatic rings. Of these the polycarbonates from di-(4-hydroxyphenyl)ether and from di-(4-hydroxy-phenyl)sulphide crystallise sufficiently to form opaque products. Both materials are insoluble in the usual solvents. The diphenyl sulphide polymer also has excellent resistance to hydrolysing agents and very low water absorption. Schnell" quotes a water absorption of only 0.09% for a sample at 90% relative humidity and 250°C. Both the sulphide and ether polymers have melting ranges of about 220-240°C. The di-(4-hydroxyphenyl)sulphoxide and the di-(4-hydroxy-phenyl)sulphone yield hydrolysable polymers but whereas the polymer from the former is soluble in common solvents the latter is insoluble. [Pg.582]

Christopher and Fox have given examples of the way in which polycarbonate resins may be tailor-made to suit specific requirements. Whereas the bis-phenol from o-cresol and acetone (bis-phenol C) yields a polymer of high hydrolytic stability and low transition temperature, the polymer from phenol and cyclohexanone has average hydrolytic stability but a high heat distortion temperature. By using a condensate of o-cresol and cyclohexanone a polymer may be obtained with both hydrolytic stability and a high heat distortion temperature. [Pg.582]

Tables. Effect of size of particles CaC03 and treatment of the filler by stearinic acid on the value of the yield strength zy of the molten polycarbonate [162]... Tables. Effect of size of particles CaC03 and treatment of the filler by stearinic acid on the value of the yield strength zy of the molten polycarbonate [162]...
Apart from that, the smaller the particle size, the stronger the structure formed by filler in the melt (that is, the yield strength of polymer ry is affected). Table 5 below demonstrates how the yield strength of molten polycarbonate composites depends on the size of CaC03 particles. [Pg.24]

Test rate and property The test rate or cross-head rate is the speed at which the movable cross-member of a testing machine moves in relation to the fixed cross-member. The speed of such tests is typically reported in cm/min. (in./min.). An increase in strain rate typically results in an increase yield point and ultimate strength. Figure 2-14 provides examples of the different test rates and temperatures on basic tensile stress-strain behaviors of plastics where (a) is at different testing rates per ASTM D 638 for a polycarbonate, (b) is the effects of tensile test-... [Pg.53]

Fig. 50. Yield for chain scission as a function of strain rate for different fractions of polycarbonate (PC) in benzyl alcohol/dioxan (90 10 v.v) at 20 °C. A normal PC with Mp = 417000 B normal PC with Mp = 321000 C normal PC with Mp = 256000 D PC with weak bonds, Mp = 217000 Mp molecular weight at peak maximum sc critical strain rate for chain scission (extrapolated from the linear portion of the degradation curve)... Fig. 50. Yield for chain scission as a function of strain rate for different fractions of polycarbonate (PC) in benzyl alcohol/dioxan (90 10 v.v) at 20 °C. A normal PC with Mp = 417000 B normal PC with Mp = 321000 C normal PC with Mp = 256000 D PC with weak bonds, Mp = 217000 Mp molecular weight at peak maximum sc critical strain rate for chain scission (extrapolated from the linear portion of the degradation curve)...
In our previous work [8], we rqjorted the synthesis of (2-oxo-l,3-dioxolan-4-yl)methacrylate (DOMA) finrn carbon dioxide and glycidyl methacrylate (GMA) using quaternary salt catalysts. In the present work, we studied the catalytic pra rmance of alkyhnethyl imidazolium salt ionic liquid in the synthesis of polycarbonate from the copolyraerization of CO2 with GMA. The influences of copolymerization variable like catalyst structure and reaction tenperature on the conversion of GMA and the yield of the polycarbonate have been discussed. [Pg.865]

Oxidative carbonylation generates a number of important compounds and materials such as ureas, carbamates, 2-oxazolidinones, and aromatic polycarbonates. The [CuX(IPr)] complexes 38-X (X = Cl, Br, I) were tested as catalysts for the oxidative carbonylation of amino alcohols by Xia and co-workers [43]. Complex 38-1 is the first catalyst to selectively prepare ureas, carbamates, and 2-oxazolidinones without any additives. The important findings were the identity of the counterion and that the presence of the NHC ligand influenced the conversions. 2-Oxazohdinones were formed from primary amino alcohols in 86-96% yield. Complex 38-1 also catalysed the oxidative carbonylation of primary amines to ureas and carbamates. n-Propylamine, n-butylamine, and t-butylamine were transformed into the... [Pg.227]

The reaction of CDI with a single mole of alcohol yields imidazole-iV-carboxyl-ates,t229H231] which by reaction with a second mole of alcohol lead to carbonic esters. With bifunctional alcohols CDI yields polycarbonic esters.[1-, C232]... [Pg.86]

With bifunctional alcohols CDI yields polycarbonates.[5] Syntheses of polycarbonates based on the CDI-method in a solid/liquid phase-transfer catalyzed reaction are described in references [261]—[263],... [Pg.91]

More active zinc phenoxide initiators of the type [Zn(0Ar)2(Et20)2]956 were found to catalyze both the copolymerization of CHO with C02 and the terpolymerization of CHO, PO, and C02 attempts to copolymerize PO and C02 yielded predominantly cyclic carbonates. For example, (332) copolymerizes CHO and C02 at 80 °C and 800 psi to give a copolymer containing 91% syndiotactic polycarbonate linkages (and 9% polyether junctions due to the non-insertion of C02) with good activity (>350g polymer/g [Zn] in 69 h).957 However, the polymerization is not well-controlled (Mw/Mn>2.5). Variation of the phenoxide ligands revealed that (333) is 4 times... [Pg.55]

Blends of flame retardant additives have been advocated as an approach to an optimum balance of properties in the finished products. For example, blends of tetrabromophthalate esters with de-cabromodiphenyl oxide or other flame retardants are reported to yield a V-0 rating in modified PPO and in polycarbonate resins without compromising melt processability or performance properties (23a-b). [Pg.245]


See other pages where Polycarbonate yield is mentioned: [Pg.596]    [Pg.261]    [Pg.371]    [Pg.400]    [Pg.366]    [Pg.596]    [Pg.261]    [Pg.371]    [Pg.400]    [Pg.366]    [Pg.2534]    [Pg.97]    [Pg.154]    [Pg.140]    [Pg.281]    [Pg.284]    [Pg.57]    [Pg.260]    [Pg.489]    [Pg.607]    [Pg.46]    [Pg.53]    [Pg.57]    [Pg.79]    [Pg.862]    [Pg.263]    [Pg.665]    [Pg.868]    [Pg.228]    [Pg.64]    [Pg.312]    [Pg.158]    [Pg.36]    [Pg.346]    [Pg.84]    [Pg.225]    [Pg.77]    [Pg.304]    [Pg.304]    [Pg.131]   


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