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Poly s polymers

Optically active bi-functionals co-polymers poly[(S)-(-)-MCPP-co-(S)-MAP-C], poly[(5)-(-)-MCPP-co-(5)-MAP-iV] and poly[(5)-(+)-MCPS-co-(S)-(+)-MOSI] were synthesized and their stmctural characterization were made. The application of this synthesized polymers are found in chiroptical switches, photoconductive as well as photorefractive and photonic materials for NLO and optical storage. [Pg.38]

These results implied that the MPA polymer responded in two different ways to the valence of the cations tested negative Cotton effects for monovalent ions and positive effects for divalent ions, thus behaving as a valence sensor for metal cations. No relationship between ionic radii and the observed selectivity bias was found and, as expected, the enantiomeric polymer [poly-(S )-2] gave the opposite results. [Pg.129]

The excellent chemical resistance and physical properties of PVA resins have resulted in broad industrial use. The polymer is an excellent adhesive and possesses solvent-, oil-, and grease-resistant properties matched by few other polymers. Poly(vinyl alcohol) films exhibit high tensile strength, abrasion resistance, and oxygen barrier properties which, under dry conditions, are superior to those of any other known polymer. The polymer s low surface tension provides for excellent emulsification and protective coUoid properties. [Pg.475]

Plasticizers. Plasticizers are materials that soften and flexibilize inherently rigid, and even britde polymers. Organic esters are widely used as plasticizers in polymers (97,98). These esters include the benzoats, phthalates, terephthalates, and trimeUitates, and aUphatic dibasic acid esters. Eor example, triethylene glycol bis(2-ethylbutyrate) [95-08-9] is a plasticizer for poly(vinyl butyral) [63148-65-2] which is used in laminated safety glass (see Vinyl POLYMERS, poly(vinyl acetals)). Di(2-ethyUiexyl)phthalate [117-81-7] (DOP) is a preeminent plasticizer. Variation of acid and/or alcohol component(s) modifies the efficacy of the resultant ester as a plasticizer. In phthalate plasticizers, molecular sizes of the alcohol moiety can be varied from methyl to tridecyl to control permanence, compatibiUty, and efficiency branched (eg, 2-ethylhexyl, isodecyl) for rapid absorption and fusion linear (C6—Cll) for low temperature flexibiUty and low volatility and aromatic (benzyl) for solvating. Terephthalates are recognized for their migration resistance, and trimeUitates for their low volatility in plasticizer appHcations. [Pg.396]

Increasing the molecular weight of polyester (or polyether) or changing its chemical composition could lower the Tg of the TPU and decrease the crystallinity of the polymer. For example, a TPU composed of poly(S-lactone), MDI, and 1,4-butanediol was found to have the lowest degree of crystallinity and, therefore, the best compatibility with PVC when the hard segment in it is 36% by weight [10]. [Pg.139]

S. V. Frolov, M. Ozaki, W. Gellermann, Z. V. Vardeny, K. Yoshino, Mirrorless lasing in conducting polymer poly(2,5-dioclyloxy-p-phenylencvinylcnc) films. Jpn. J. Appl. Phys. 1996, 35, L1371. [Pg.178]

Ebdon and coworkers22 "232 have reported telechelic synthesis by a process that involves copolymerizing butadiene or acetylene derivatives to form polymers with internal unsaturation. Ozonolysis of these polymers yields di-end functional polymers. The a,o>dicarboxy1ic acid telechelic was prepared from poly(S-s tot-B) (Scheme 7.19). Precautions were necessary to stop degradation of the PS chains during ozonolysis. 28 The presence of pendant carboxylic acid groups, formed by ozonolysis of 1,2-diene units, was not reported. [Pg.380]

Figure 35. Dynamic change of lifetime in an n-type silicon/polymer (poly(epichlorhydrine-co-elhylenoxide-co-allyl-glycylether plus iodide) junction during a potential sweep. The arrows show the direction of sweep (0.25 V s" ). A shoulder in the accumulation region and a peak in the depletion region of silicon are clearly seen. Figure 35. Dynamic change of lifetime in an n-type silicon/polymer (poly(epichlorhydrine-co-elhylenoxide-co-allyl-glycylether plus iodide) junction during a potential sweep. The arrows show the direction of sweep (0.25 V s" ). A shoulder in the accumulation region and a peak in the depletion region of silicon are clearly seen.
Figure 4. (A) Cyclic voltammograms over a range of scan rates for a redox polymer (poly-[Fe 5-amino-1,10-phenanthrotme)3]3+/>)91 and (B) p-doping and undoping of a conducting polymer (polypyrrole) (B). [(A) Reprinted from X. Ren and P. O. Pickup, Strong dependence of the election hopping rate in poly-tris(5-amino-1,10-phenan-throline)iron(HI/II) on the nature of the counter-anion J. Electroanal. Chem. 365, 289-292,1994, with kind permission from Elsevier Sciences S.A.]... Figure 4. (A) Cyclic voltammograms over a range of scan rates for a redox polymer (poly-[Fe 5-amino-1,10-phenanthrotme)3]3+/>)91 and (B) p-doping and undoping of a conducting polymer (polypyrrole) (B). [(A) Reprinted from X. Ren and P. O. Pickup, Strong dependence of the election hopping rate in poly-tris(5-amino-1,10-phenan-throline)iron(HI/II) on the nature of the counter-anion J. Electroanal. Chem. 365, 289-292,1994, with kind permission from Elsevier Sciences S.A.]...
The requirements outlined above represent a considerable challenge for polymer synthesis. This article describes an appealing development, based on two central substance-classes of conjugated polymers, poly(para-phenylene)s and poly(para-phenylenevinylene)s. [Pg.165]

Enzymes are generally classified into six groups. Table 1 shows typical polymers produced with catalysis by respective enzymes. The target macromolecules for the enzymatic polymerization have been polysaccharides, poly(amino acid)s, polyesters, polycarbonates, phenolic polymers, poly(aniline)s, vinyl polymers, etc. In the standpoint of potential industrial applications, this chapter deals with recent topics on enzymatic synthesis of polyesters and phenolic polymers by using enzymes as catalyst. [Pg.206]

J. Pei, W.-L. Yu, W. Huang, and A.J. Heeger, The synthesis and characterization of an efficient green electroluminescent conjugated polymer poly[2,7-h s(4-hexylthienyl)-9,9-dihexylfluorene], Chem. Commune. 1631-1632, 2000. [Pg.277]

C.C. Wu, P.Y. Tsay, H.Y. Cheng, and S.J. Bai, Polarized luminescence and absorption of highly oriented, fully conjugated, heterocyclic aromatic rigid-rod polymer poly-p-phenylenebenzoxazole, J. Appl. Phys., 95 417 123, 2004. [Pg.292]

The solubility is generally improved by the introduction of fluorine atoms into aromatic condensation polymers. Poly(carbonate)s containing hexafluoroisopropylidene units are much more soluble than Bisphenol A poly(carbonate) (3). All of the hexafluoroisopropylidene-unit-containing poly(carbonate)s become soluble in acetone, ethyl acetate, chloroform, and dimethyl sulfoxide (DMSO) in addition to the solvents of Bisphenol A poly(carbonate) (3). Colorless, transparent, and flexible films are prepared from hexafluoroisopropylidene-unit-containing poly(carbonate)s by casting or pressing. [Pg.131]


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See also in sourсe #XX -- [ Pg.358 , Pg.359 ]

See also in sourсe #XX -- [ Pg.169 , Pg.170 , Pg.182 , Pg.220 ]




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Poly polymers

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