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Poly aging

Poly(vinyl cinnamate) Resists. Dichromated resists exhibit numerous shortcomings which include lot-to-lot variabiUty of the components, aging of the formulated resists in solution and in coated form, poor process stabiUty (due to a sensitivity to variations in temperature and humidity), and intrinsically low photosensitivity requiring long exposure times for adequate insolubilization. [Pg.115]

Fig. 7. Effect of aging on solution vicosity of poly(vinyl alcohol) (60), where A represents DP = 1500, 98—99 mol % hydrolyzed and B, DP = 1500, 87—89... Fig. 7. Effect of aging on solution vicosity of poly(vinyl alcohol) (60), where A represents DP = 1500, 98—99 mol % hydrolyzed and B, DP = 1500, 87—89...
There are no significant health hazards arising from exposure to poly(vinyl chloride) at ambient temperature (154—158). However, a British study has found a small decrease in breathing capacity for workers who smoked and were exposed to vinyl resin dust (159). This decrease was about one-seventh of that caused by normal aging and about equal to that expected with a one-pack-a-day cigarette smoker. [Pg.508]

Epichlorohydrin Elastomers without AGE. ECH homopolymer, polyepichlorohydrin [24969-06-0] (1), and ECH—EO copolymer, poly(epichlorohydrin- (9-ethylene oxide) [24969-10-6] (2), are linear and amorphous. Because it is unsymmetrical, ECH monomer can polymerize in the head-to-head, tail-to-tail, or head-to-tail fashion. The commercial polymer is 97—99% head-to-tail, and has been shown to be stereorandom and atactic (15—17). Only low degrees of crystallinity are present in commercial ECH homopolymers the amorphous product is preferred. [Pg.553]

AGE-Gontaining Elastomers. ECH—AGE, poly(epichlorohydrin-fo-allyl glycidyl ether) [24969-09-3] (3), ECH—EO—AGE, poly(epichlorohydrin- (9-ethylene oxide-i (9-allyl glycidyl ether) [26587-37-1] (4), ECH—PO—AGE, and PO—AGE are also amorphous polymers. [Pg.553]

Crystallinity is low the pendent allyl group contributes to the amorphous state of these polymers. Propylene oxide homopolymer itself has not been developed commercially because it cannot be cross-baked by current methods (18). The copolymerization of PO with unsaturated epoxide monomers gives vulcanizable products (19,20). In ECH—PO—AGE, poly(ptopylene oxide- o-epichlorohydrin- o-abyl glycidyl ether) [25213-15-4] (5), and PO—AGE, poly(propylene oxide-i o-abyl glycidyl ether) [25104-27-2] (6), the molar composition of PO ranges from approximately 65 to 90%. [Pg.554]

Molecular weight determinations of ECH—EO, ECH—AGE, ECH—EO—AGE, ECH—PO—AGE, and PO—AGE have not been reported. Some solution studies have been done on poly(propylene oxide), and these may approximate solution behavior of the PO—AGE copolymer (33,34). [Pg.555]

There are a number of occasions where a transparent plastics material which can be used at temperatures of up to 150°C is required and in spite of its relatively high cost, low impact strength and poor aging properties poly-(4-methylpent-1 -ene) is often the answer. Like poly(vinyl chloride) and polypropylene, P4MP1 is useless without stabilisation and as with the other two materials it may be expected that continuous improvement in stabilising antioxidant systems can be expected. [Pg.273]

Polymers with very good heat resistance (both in terms of deformation and of heat aging resistance) but which may be processed by conventional techniques, e.g. polysulphones and poly(phenylene oxides). [Pg.611]

The chemical name for such materials is poly(bisbenzimid-azobenzophenan-throlines) but they are better known as BBB materials. Such polymers have a Tg in excess of 450°C and show only a low weight loss after aging in air for several hundred hours at 370°C. Measurements using thermal gravimetric analysis indicate a good stability to over 600°C. The main interest in these materials is in the field of heat-resistant films and fibres. [Pg.848]

Fig. 7. Voigt model analysis of (a) lateral contact stiffness and (b) the response time, t, for a silicon nitride tip vs. poly(vinylethylene) as a function of frequency and polymer aging times. Reprinted with permission from ref [71]. Fig. 7. Voigt model analysis of (a) lateral contact stiffness and (b) the response time, t, for a silicon nitride tip vs. poly(vinylethylene) as a function of frequency and polymer aging times. Reprinted with permission from ref [71].
Polyesters and polycarbonate polyols show improved resistance to oxidative attack, compared with that of the polyethers. Stress relation studies run at 130°C, comparing a urethane based on a poly(oxypropylene) polyol and a urethane based on poly(butane adipate) polyol show that, after 60 h, the urethane based on PPG lost most of its strength, while the polyester retained most of its strength [83], Urethanes made from poly(butadiene) polyols are also susceptible to oxidation, but they show good resistance to air-oven aging with antioxidants present (see p. 290 in [45],... [Pg.803]

Moreover, calculations on the evaporation rate of bromine from the complex phase were carried out assuming a worst-case scenario, namely a complete spill age of the total bromine inventory (as poly bromide complex) of a fully charge (100% SOC) 15 kWh module which means -32.5 kg of available Br2, forming a 10 m2... [Pg.189]

B. Chemical Factors Contributing to Aging Many propint systems have built-in defects which contribute to degradation of the polymer system and reduce service life. The poly are ... [Pg.906]

Polylactides, 18 Poly lactones, 18, 43 Poly(L-lactic acid) (PLLA), 22, 41, 42 preparation of, 99-100 Polymer age, 1 Polymer architecture, 6-9 Polymer chains, nonmesogenic units in, 52 Polymer Chemistry (Stevens), 5 Polymeric chiral catalysts, 473-474 Polymeric materials, history of, 1-2 Polymeric MDI (PMDI), 201, 210, 238 Polymerizations. See also Copolymerization Depolymerization Polyesterification Polymers Prepolymerization Repolymerization Ring-opening polymerization Solid-state polymerization Solution polymerization Solvent-free polymerization Step-grown polymerization processes Vapor-phase deposition polymerization acid chloride, 155-157 ADMET, 4, 10, 431-461 anionic, 149, 174, 177-178 batch, 167 bulk, 166, 331 chain-growth, 4 continuous, 167, 548 coupling, 467 Friedel-Crafts, 332-334 Hoechst, 548 hydrolytic, 150-153 influence of water content on, 151-152, 154... [Pg.597]

In the case of undoped PVCa films, impurities and surface states dominate the photoconduction mechanism (6) leading one to question any study of intrinsic pKotoconduction in organic polymers. Poly(N-vinylcarbazole) films yellow under ambient laboratory conditions. Work in our laboratory (7) has shown that ageing of a purified sample of PVCa leads to an increase in photoresponse in the 350-450 nm region while there is an initial drop in photoresponse in the 250-... [Pg.138]


See other pages where Poly aging is mentioned: [Pg.377]    [Pg.426]    [Pg.281]    [Pg.329]    [Pg.327]    [Pg.399]    [Pg.477]    [Pg.463]    [Pg.471]    [Pg.297]    [Pg.124]    [Pg.510]    [Pg.580]    [Pg.586]    [Pg.661]    [Pg.35]    [Pg.531]    [Pg.551]    [Pg.929]    [Pg.116]    [Pg.804]    [Pg.289]    [Pg.396]    [Pg.34]    [Pg.140]    [Pg.10]    [Pg.110]    [Pg.280]    [Pg.163]    [Pg.537]    [Pg.190]    [Pg.186]   
See also in sourсe #XX -- [ Pg.164 , Pg.166 ]




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