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Divinylbenzene sulfonation

Membranes may be manufactured by mixing powdered ion exchange resin with a solution of binder polymer and pouring the heated mixture under pressure onto a plastic mesh or cloth. The concentration of the ion exchanger is normally 50-70%. They are chiefly copolymers of styrene and divinylbenzene, sulfonated with sulfuric acid for introduction of the cation exchange group. [Pg.510]

Ag and Co functionalized adsorbents for the PPhs adsorption. These transition-metal functionalized adsorbents were prepared by immobilizing Ag and Co onto a solid carrier, for which Amberlyst IS has been selected. Amberlyst 15, a macroreticular polystyrene - crosslinked by divinylbenzene - sulfonated cation exchange resin, has been selected as carrier because of its large pore diameter of approximately 100 [nm]. These macropores ensure the accessibility for the relatively large PPh3 ligands. [Pg.293]

C-150 is macroporous styrene—divinylbenzene sulfonate produced by Purolite Int. (UK). Source After [420]. [Pg.613]

Combination techniques such as microscopy—ftir and pyrolysis—ir have helped solve some particularly difficult separations and complex identifications. Microscopy—ftir has been used to determine the composition of copolymer fibers (22) polyacrylonitrile, methyl acrylate, and a dye-receptive organic sulfonate trimer have been identified in acryHc fiber. Both normal and grazing angle modes can be used to identify components (23). Pyrolysis—ir has been used to study polymer decomposition (24) and to determine the degree of cross-linking of sulfonated divinylbenzene—styrene copolymer (25) and ethylene or propylene levels and ratios in ethylene—propylene copolymers (26). [Pg.148]

Unlike earlier sulfonated styrene/divinylbenzene copolymers, these sulfonated gels can he run in virtually any solvent from water and buffers to pure organics as well as most any mixed solvent systems desired. In aqueous systems they absorb water and in organic solvents they stay swollen by imbibing organic solvents. [Pg.374]

A sulfonated ion exchanger catalyst (Research Institute of Synthetic Resins and Varnishes, Pardubice, Czechoslovakia) was a macroreticular styrene-divinylbenzene copolymer containing 25% divinylbenzene and 2.4 meq/g of —SO3H groups. It was dried prior to using at 90°C/14 Torr. The BET surface area, determined in a dry state, was 49 m2/g, and the mean pore size was around 100 A. [Pg.27]

The organic resin material is often a styrene divinylbenzene (DVB) copolymer in a network or matrix, to which are attached functional groups such as a sulfonic acid, carboxylic acid, and quaternary ammonium. The nature of these groups determines whether the resin is classified as a strong/weak acid (cation resin) or strong/weak base (anion resin) ion-exchanger. [Pg.327]

Finally, ion chromatography can be used to determine the a-sulfo fatty acid esters. The chromatographic column is a nonpolar poly sty rene/divinylbenzene column and the ion pair reagent is 0.005 M ammonia. In order to reduce the elution time, acetonitrile is added as a modifier with increasing concentration. This gradient technique makes it possible to separate simultaneously ester sulfonates and disalts by chain length. Determination is achieved by standards with defined chain length [107]. [Pg.493]

Very recent relevant observations reveal that the TCS approach albeit certainly significant as conceptual and operational tool in the issue of metal nanoclusters size control, requires a substantial further perfection. Resin sulfonated Bayer K1221 is a co styrene-divinylbenzene commercially available gel-type resin, in beaded form. Its cross-linking degree is ca. 4% mol and therefore K1221 is expectedly quite similar to DOMA-VP and MTEMA-DMAA 4-4 for example. In fact ISEC analysis reveals a nanoporosity featured by 4.0 and 2.0 nm nanopores only. The expectation is that a Pd°/K1221 nanocomposite obtained with a classic procedure [5,9,10] will exhibit diameters strictly ranging from 2 to 4 nm. [Pg.415]

The polyamines putrescine, cadaverine, spermidine, and spermine, which are seen at elevated levels in some victims of cancer, were separated on a Technicon (The Technicon Company Chauncey, NY) TSM Amino Acid Analyzer packed with an 8% divinylbenzene-co-polystyrene sulfonated resin with post-column ninhydrin detection.111 Amines such as ethanolamine, noradrenaline, hexamethylene diamine, methoxytryptamine, spermine, and spermidine were separated from amino acids on a DC-4A cation exchange resin.112 A similar approach, using a Beckman Model 121M amino acid analyzer equipped with an AA-20 column, was also successful.113 A Polyamin-pak strong cation exchange column (JASCO) was eluted with a citrate buffer for the detection of putrescene, spermine, cadaverine, and 1,5-diaminohex-ane from rat thymus.114 A post-column o-phthaldehyde detection system was used. [Pg.230]

Sulfonated styrene divinylbenzene. d Polysulfonated styrene divinylbenzene. e Polysulfonated 4-clorostyrene divinylbenzene. [Pg.341]

Waters Oasis Sulfonated divinylbenzene- Mixed mode with strong Alkaloids (83) illicit drugs... [Pg.7]

Ion exchange resins based on poly(styrene-divinylbenzene) backbones display mixed mode retention mechanisms. The ion exchange functionality (sulfonic acid or carboxylic acid for cation exchangers and quartemary or primary, secondary, or tertiary amines for anion exchangers) contributes to the ionic mechanism and the backbone polymer to hydrophobic retention. This is exemplified... [Pg.7]

See also Macroreticular sulfonated styrene-divinylbenzene copolymers... [Pg.894]

Sulfonated poly(styrene-divinylbenzene) ion- exchange resins, manufacture of, 23 536... [Pg.901]

Sulfonated styrene-divylbenzene copolymers. See Styrene-divinylbenzene copolymers, sulfonated Sulfonate moeities, incorporation into polymers, 23 534, 535 Sulfonate surfactants, 24 146 Sulfonating reagents composition of, 23 520t indirect, 23 522-523t Sulfonation, 9 273-275, 313, 23 513-536, 12 181... [Pg.901]

FIGURE I Schematic diagram illustrating the construction of an anion exchange latex coated, surface-sulfonated, nonporous cross-linked polyethylvinylbenzene-divinylbenzene resin bead. [Pg.223]

One of the earliest proton exchange membranes was based on sulfonated polystyrene where divinylbenzene was used as a cross-linking unit for extra stability. Developed by General Electric, this membrane (21) was cheap and easy to manufacture, and it was used for fuel cells in the Gemini space pro-gram.i However, due to the sensitivity of the benzylic hydrogen to radical attack, lifetimes for these membranes under FC operating conditions were quite low. Thus, little work has been carried out on these systems since their inception. [Pg.149]


See other pages where Divinylbenzene sulfonation is mentioned: [Pg.3]    [Pg.3]    [Pg.945]    [Pg.253]    [Pg.11]    [Pg.87]    [Pg.376]    [Pg.452]    [Pg.67]    [Pg.308]    [Pg.417]    [Pg.175]    [Pg.341]    [Pg.218]    [Pg.289]    [Pg.492]    [Pg.337]    [Pg.338]    [Pg.15]    [Pg.27]    [Pg.119]    [Pg.64]    [Pg.54]    [Pg.131]    [Pg.325]   
See also in sourсe #XX -- [ Pg.222 ]




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Divinylbenzene

Divinylbenzene-cross-linked polystyrene sulfonated

Divinylbenzenes

Structure sulfonated styrene/divinylbenzene

Sulfonated polystyrene-divinylbenzene

Sulfonated polystyrene-divinylbenzene copolymer membranes

Sulfonated styrene/divinylbenzene

Sulfonation of styrene divinylbenzene

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