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Hydrogenated polymers

Types of starting polymers Unhydrogenated precursor Hydrogenated polymer ... [Pg.168]

E. B. Brandes and F. C. Loveless. Dispersants and dispersant viscosity index improvers from selectively hydrogenated polymers. Patent WO... [Pg.362]

For the partially hydrogenated polymers, the reaction was quenched by adding 2-propanol. [Pg.397]

Further confirmation of the structure and tacticity of poly/5-methyl-l,4-hexadiene)was obtained from X-ray diffraction and u-NMR data of its hydrogenated polymer (Scheme 2). The hydrogenated polymer sample showed a highly crystalline pattern (Figure 7), with diffraction spots that were well defined. This pattern was identical to that of isotactic poly(5-methyl-l-hexene) as reported in the literature (26) (measured identity period, 6.2 A lit., 6.33 A). [Pg.181]

The C-NMR spectrum of the hydrogenated polymer sample in CDClj solvent (Figure 8) was identical to that of the polymer we obtained by the direct polymerization of 5-methyl-1-hexene with Et2AlCl/6-TiCl3 AA catalyst (Al/Ti atomic ratio = 1.5, hexane solvent, 30°C). The hydrogenation was essentially complete. [Pg.183]

Hydrogenated polymers have many desirable properties over their parent polymers, although the high cost of hydrogenated products still restricts their widespread application. The following aspects should be considered for the sustainable development of the hydrogenated polymer industry ... [Pg.579]

The development of highly efficient and easily recoverable catalyst systems. Today, the high cost of hydrogenated polymers is due mainly to the cost of the metal catalyst and its recovery operation. [Pg.579]

CHA-CH=CH-CHB-CHA-CH=CH-CHB-. The hydrogenated polymers may analogously be considered —CHA—CH2 CH2—CHB—CHA— CH2—CH2—CHB—. In these cases the complexity of the disubstituted polymer adds to that of the polymers in which the two chain directions are different. In principle 4 two-center, 8 three-center, and 16 four-center sequences must be considered. [Pg.27]

The method has been applied to saturated aromatic and olefin-free mineral oil fractions and hydrogenated polymers cf. Table III and IV). [Pg.59]

Table IV contains data on hydrogenated polymers of propylene, isobutene and cyclohexene obtained by polymerization under various conditions38. The Direct Method (ultimate analysis and molecular weight) shows that the polymers of propylene and isobutene are paraffinic for the estimation of cp the appropriate formulas were used. In the case of the highly cyclic saturated cyclohexene-polymers the formulas for hydrogenated mineral oil fractions were applied. In the table are also given values of q> and Rt determined with the ring analysis diagrams of Figs. 59 and 60 (p. 64-65). Table IV contains data on hydrogenated polymers of propylene, isobutene and cyclohexene obtained by polymerization under various conditions38. The Direct Method (ultimate analysis and molecular weight) shows that the polymers of propylene and isobutene are paraffinic for the estimation of cp the appropriate formulas were used. In the case of the highly cyclic saturated cyclohexene-polymers the formulas for hydrogenated mineral oil fractions were applied. In the table are also given values of q> and Rt determined with the ring analysis diagrams of Figs. 59 and 60 (p. 64-65).
Individual enantiomers of 90 have been prepared by RCM (Section VII.A.l) and polymerized by 8 (R = Ph) at — 30 °C to give a 52% yield of a 74% trans polymer226. Likewise 91, with the same initiator at — 55 °C, gives a 51% yield of 60% cis polymer, with a blocky cis/trans distribution (rtrc = 6.3) the 13C NMR spectrum of the hydrogenated polymer shows it to be atactic326. [Pg.1547]

Poly(vinylidene fluoride) (PVDF) is the second most important thermoplastic within the fluoropolymer family after PTFE. Although, both the thermal and chemical stability of PVDF are somewhat lower compared to PTFE, the hydrogenated polymer can be more easily processed with conventional equipment, and it offers an advantageous compromise between quality and price. When the... [Pg.23]

Attempts to reduce PPEs 12 under moderate pressures (2-3 bar H2) at temperatures of around 70-80 °C were unsuccessful. PPEs seem to be very stable chemically, and only when the reduction was performed in an autoclave under drastic conditions successful hydrogenation was observed. Hydrogen pressures of 300-500 bar at temperatures of around 300 °C are necessary for complete reduction of the PPE to the hydrogenated polymer 60 [40]. The yield of 60 is high the aromatic rings are not affected under these conditions and side products are not detected in the colorless materials formed. Attempts to use shorter reaction times, lower temperatures, or lower hydrogen pressures failed, and partially reacted material of undefined structure resulted. [Pg.230]


See other pages where Hydrogenated polymers is mentioned: [Pg.878]    [Pg.556]    [Pg.561]    [Pg.562]    [Pg.567]    [Pg.567]    [Pg.569]    [Pg.570]    [Pg.167]    [Pg.132]    [Pg.103]    [Pg.550]    [Pg.550]    [Pg.568]    [Pg.570]    [Pg.575]    [Pg.577]    [Pg.578]    [Pg.578]    [Pg.579]    [Pg.441]    [Pg.219]    [Pg.415]    [Pg.50]    [Pg.14]    [Pg.60]    [Pg.60]    [Pg.1540]    [Pg.1541]    [Pg.1546]    [Pg.1574]    [Pg.175]    [Pg.899]   
See also in sourсe #XX -- [ Pg.211 , Pg.212 ]




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Acid-containing polymers, hydrogen

Acid-containing polymers, hydrogen bonding

Addition polymers hydrogen halides

Block polymers hydrogen bonding units

Butadiene polymers, hydrogenation

Carbon Hydrogen Polymers

Carbon-Hydrogen-Type Polymers

Cross-linked polymers hydrogen bonding

Diene polymers, hydrogenated

Diene polymers, hydrogenation

Effect of Hydrogen Bonding in Polymer Blends on Nano-Morphology

High-performance polymers Hydrogenated poly

Hydrogen Bonding Interactions Self-Sorting on Polymers

Hydrogen PEFCs solid polymer electrolyte

Hydrogen atom transfer from polymer

Hydrogen bond acidic functionalized polymers

Hydrogen bond polymer architectures

Hydrogen bonding in polymer blends

Hydrogen bonding polymers

Hydrogen bonding ring containing polymers

Hydrogen bonding synthetic polymers

Hydrogen bonding water with amorphous polymer

Hydrogen bonding, in polymers

Hydrogen bonds in polymers

Hydrogen bonds, in nanostructured polymer blends

Hydrogen bonds/bonding coordination polymers

Hydrogen cyanide, from decomposition polymers

Hydrogen intrinsically conducting polymers

Hydrogen polymers

Hydrogen production polymer-electrolyte membrane

Hydrogen supramolecular polymers

Hydrogen termination polymer deposition

Hydrogen, bond dissociation energy polymers

Hydrogen, energy conversion polymer electrolyte fuel cell

Hydrogen-bonded chain polymer

Hydrogen-bonded interpenetrating polymer networks

Hydrogen-bonded polymers

Hydrogen-bonded supramolecular polymers

Hydrogen-bonded supramolecules polymer-based

Hydrogen-bonding liquids amorphous polymers

Hydrogenated SBS triblock polymers

Hydrogenated polymers, applications

Hydrogenated polymers, ruthenium-based

Hydrogenated styrene-diene polymers

Hydrogenation of polymers

Hydrogenation polymer resistance

Hydrogenation polymer-bound catalysts

Hydrogenation using polymer supported catalysts

Hydrogenation with polymer-bound phosphines

Inter-polymer hydrogen bonds

Liquid crystalline polymers hydrogen bonding

Main Chain Hydrogen-Bonded Polymers

Main chain polymers, hydrogen bonding

Nano-Morphology Formation in Polymer Blends without and with Hydrogen Bonding

Organic-Inorganic Polymer Hybrids Through Hydrogen Bonding

Organometallic polymers hydrogenation catalyst

Polymer aldehydes, transfer hydrogenation

Polymer blends, hydrogen bonding

Polymer cross-linking, hydrogen-bonded

Polymer electrolyte fuel cells Hydrogen PEFCs

Polymer electrolyte membrane hydrogen oxidation

Polymer formation chain initiation, hydrogen

Polymer from polydiene, hydrogenated

Polymer hydrogenous polyisoprene

Polymer modifications hydrogenation

Polymer resin hydrogenation methods

Polymer-based hydrogenation catalyst

Polymer-supported reagents alkene hydrogenation

Polymers Connected with Bivalent Hydrogen Bonds

Polymers Connected with Multiple Hydrogen Bonds

Polymers Connected with Quadruple Hydrogen Bonds

Polymers Connected with Trivalent Hydrogen Bonds

Polymers bivalent hydrogen bonds

Polymers hydrogenation catalyst supports

Polymers multiple hydrogen bonds

Polymers quadruple hydrogen bonds

Polymers side-chain hydrogen-bonded

Polymers trivalent hydrogen bonds

Polymers with Hydrogen-Bonding Motifs

Polymers with hydrogen bond chains

Polymers, hydrogenation

Polymers, hydrogenation

Self-Assembly of Supramolecular Polymers via Hydrogen Bonds

Self-assembly with hydrogen bonding polymers

Side polymers, hydrogen-bonded

Solid polymer electrolyte electrolytic hydrogen generating

Supramolecular polymer networks hydrogen bonding

Synthesis and Self-Assembly of Hydrogen-Bonded Supramolecular Polymers

Synthetic Strategies Towards Hydrogen-Bonded Supramolecular Polymers

Synthetic polymer gels hydrogen bond networks

Telechelic Hydrogen Bond Functional Polymers

The Hydrogenation of Polymers

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