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Polymer benzenes

P-p-C H4Ph2CCl, Pyr, 25°, 5 days, 90%, where P = styrene-divinyl-benzene polymer. Triarylmethyl ethers of primary hydroxyl groups in glucopyranosides have been prepared using a polymeric form of triphenylmethyl chloride. Although the yields are not Improved, the workup is simplified. [Pg.102]

HPLC of aqueous simulants or water using an ion exclusion column (styrene divinyl benzene polymer with sulfonated [cationic] ion-exchange groups). Derivitisation with fluorescamine, 4-phenylspiro-[furan 2-(3),... [Pg.601]

Measured in Benzene, Polymer Bank Data Sheet. [Pg.146]

At room temperature, these molecules occupy well-defined locations in their respective crystal lattices. However, they tumble freely and isotropically (equally in all directions) in place at their lattice positions. As a result, their solid phase NMR spectra show features highly reminiscent of liquids. We will see an illustration of this point shortly. Other molecules may reorient anisotropically (as in solid benzene). Polymer segmental motions in the melt may cause rapid reorientation about the chain axis but only relatively slow reorientation of the chain axes themselves. Large molecular aggregates in solution (such as surfactant micelles or protein complexes or nucleic acids) may appear to have solidlike spectra if their tumbling rates are sufficiently slow. There are numerous other instances in which our macroscopic motions of solid and liquid may be at odds with the molecular dynamics. Nuclear magnetic resonance is one of the foremost ways of investigating these situations. [Pg.286]

Mobil/Badger Ethylbenzene Benzene, polymer-grade ethylene EBMax process uses proprietary Mobil MCM-22 zeolite catalyst low capital cost 10 2000... [Pg.128]

Booth, C. Devoy, C. J., "Thermodynamics of Mixtures of Polyethylene oxide) and Benzene," Polymer, 12, 309 (1971a). [Pg.167]

Q,C,atropine, acridine.ephe-drine,opium alkaloids,reserpine,strychnine, yohimbine Separation on styrene-divinyl benzene polymer (Table 8.4) - Hitachi gel 3010, 10 pm 220x4.6 ACN-0.02M NH,0H(3 2) ACN-0.02M tetrabutyl-ammoniumhydroxide (3 7), (3 2) 44... [Pg.281]

Porous styrene-divinyl no detailsMeOH-NH.OH benzene polymer or ... [Pg.471]

Figure 23. FTIR (ATR) spectrum of benzene polymer prepared under Condition B (see Table 1)... Figure 23. FTIR (ATR) spectrum of benzene polymer prepared under Condition B (see Table 1)...
F. D Alelio, of General Electric Co., prepared the first styrene-divinyl benzene polymers (U.S. Patents 2,340,110 and 2,340,111). These allowed various porosities of material to be prepared and provided a backbone for various types of cation and anion exchange groups to be added. (See the reaction on p. 271.)... [Pg.270]

One type of anion exchange column used for nonsuppressed applications is the ION-20 from Interaction Co. It is a quaternary ammonium group on a styrene-divinyl benzene polymer in the form of 9 pm particles with an exchange capacity of 100 peq/g. Figure 24-14 is an example of a multiple anion separation. [Pg.286]

The two insoluble compounds precipitate and are removed from the water by filtration. Thus by the successive usage of cation and anion-exchange resins sodium chloride could be removed from water. An example of a cation-exchange resin is sulfonated styrene-divinyl-benzene polymer and an anion-exchange resin can be made by chloromethylating styrene-divinyl copolymer and replacing the chlorines with tr i me thy1ami ne. [Pg.1105]

Ouinone-impreg-nated styrene-divinyl benzene polymers... [Pg.190]

Odian, G., 2004b. Principles of Polymerization, 4th ed. Wiley-Interscience, Hoboken, New Jersey. OhUnger, R., Bandermann, F., 1980. Kinetics of the propagation reaction of butadiene-styrene copolymerization with Uthium-a-ganic compounds. Macromol. Chem. 181 (9), 1935-1947. Oishi, Y., Watanabe, H., Kanaya, T., et al., 2006. Dynamics of monofunctional polybutadienyl lithium chains aggregated in benzene. Polym. J. 38 (3), 277-288. [Pg.109]

A flammability test under a 50 % oxygen atmosphere was also carried out. The vinyl polymer 1, ferrocene 6b and benzene polymers 7 are burned out when attacked with flame. The carborane hybrids 3a, 3b are both ignited but extinguished soon in the case of the higher (y + z) contents. The introduction of carborane brings non-flammability to the hybrid polymers along with thermal and mechanieal strength. Transformation of the boron structure to boron oxide was observed around... [Pg.624]


See other pages where Polymer benzenes is mentioned: [Pg.2030]    [Pg.60]    [Pg.491]    [Pg.491]    [Pg.286]    [Pg.67]    [Pg.68]    [Pg.305]    [Pg.239]    [Pg.1788]    [Pg.1282]    [Pg.232]    [Pg.388]    [Pg.529]    [Pg.1106]    [Pg.2222]    [Pg.160]    [Pg.321]    [Pg.198]    [Pg.2206]    [Pg.2034]    [Pg.200]    [Pg.312]    [Pg.209]    [Pg.165]   
See also in sourсe #XX -- [ Pg.232 ]




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Polymers benzene oxidation route

Polymers benzene-sulfur containing

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Styrene-divinyl benzene polymers

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