Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ion-exchange modification

Another aspect to zeohte catalytic activity, briefly mentioned earlier, is the use of ion-exchange modification to introduce elements of known catalytic propensity into the zeolite promoter. Examples of this are in Table 31. There has been a considerable amount of work devoted to the investigation of the dispersion of metal particles (e.g. Ni and Fe) on zeolite substrates to enhance specific organic reactions. [Pg.5108]

The esterification reaction can also be carried out in CMRs. The catalytic membranes are prepared by ion exchange modification. CMRs may outperform PVMRs in conversion with the same loading of catalyst dispersed in the liquid bulk [38]. [Pg.93]

Structure Modification. Several types of stmctural defects or variants can occur which figure in adsorption and catalysis (/) surface defects due to termination of the crystal surface and hydrolysis of surface cations (2) stmctural defects due to imperfect stacking of the secondary units, which may result in blocked channels (J) ionic species, eg, OH , AIO 2, Na", SiO , may be left stranded in the stmcture during synthesis (4) the cation form, acting as the salt of a weak acid, hydrolyzes in aqueous suspension to produce free hydroxide and cations in solution and (5) hydroxyl groups in place of metal cations may be introduced by ammonium ion exchange, followed by thermal deammoniation. [Pg.447]

Catalytic Properties. In zeoHtes, catalysis takes place preferentially within the intracrystaUine voids. Catalytic reactions are affected by aperture size and type of channel system, through which reactants and products must diffuse. Modification techniques include ion exchange, variation of Si/A1 ratio, hydrothermal dealumination or stabilization, which produces Lewis acidity, introduction of acidic groups such as bridging Si(OH)Al, which impart Briimsted acidity, and introducing dispersed metal phases such as noble metals. In addition, the zeoHte framework stmcture determines shape-selective effects. Several types have been demonstrated including reactant selectivity, product selectivity, and restricted transition-state selectivity (28). Nonshape-selective surface activity is observed on very small crystals, and it may be desirable to poison these sites selectively, eg, with bulky heterocycHc compounds unable to penetrate the channel apertures, or by surface sdation. [Pg.449]

Tetramethylammonium hydroxide (5H2O) [10424-65-4 (5H2O), 75-59-2 (aq soln) ] M 181.2, m 63°, 65-68°. Freed from chloride ions by passage through an ion-exchange column (Amberlite IRA-400, prepared in its OH" form by passing 2M NaOH until the effluent was free from chloride ions, then washed with distilled H2O until neutral). A modification, to obtain carbonate-free hydroxide, uses the method of Davies and Nancollas [Nature 165 237 1950]. [Pg.363]

This sample preparation involves the decomposition of the fungicide (sodium hydroxymethylglycinate) into sodium glycinate and represents the type of sample that requires significant modification before it can be chromatographed. After decomposition it is then separated by ion exchange chromatography. [Pg.223]

Ion chromatography can be used in unique ways and by appropriate modification can often be applied to the separation of mixtures where the components themselves do not ionize or do not normally produce interactive ions in aqueous solution. A good example of this type of separation is afforded by the analysis of saccharide mixtures using ion exchange interactions. An illustration of such a separation is given in figure 15. [Pg.312]

Klotzbach T, WattM, Ansari Y, Minteer SD. 2006. Effects of hydrophobic modification of chit-osan and Nafion on transport properties, ion-exchange capacities, and enzyme immobilization. J Membrane Sci 282 276-283. [Pg.632]

Surface Adsorption Hater sample is passed through a column of the adsorbent and the adsorbed organic constituents subsequently eluted with a smaller volume of organic solvent. All sample types Adsorbents Include charcoal, macroretlcular resins, polyurethane foams, bonded phases and ion-exchangers. Generally have high capacity but sample discrimination may be a -problem. Sample modification and Incomplete recovery are further possible problems. [Pg.376]


See other pages where Ion-exchange modification is mentioned: [Pg.351]    [Pg.83]    [Pg.351]    [Pg.83]    [Pg.2776]    [Pg.2784]    [Pg.2785]    [Pg.197]    [Pg.565]    [Pg.384]    [Pg.387]    [Pg.140]    [Pg.280]    [Pg.194]    [Pg.314]    [Pg.2030]    [Pg.2143]    [Pg.255]    [Pg.440]    [Pg.3]    [Pg.13]    [Pg.233]    [Pg.165]    [Pg.113]    [Pg.118]    [Pg.352]    [Pg.30]    [Pg.31]    [Pg.31]    [Pg.161]    [Pg.19]    [Pg.140]    [Pg.214]    [Pg.226]    [Pg.144]    [Pg.63]    [Pg.67]    [Pg.154]    [Pg.162]    [Pg.175]    [Pg.199]    [Pg.102]   
See also in sourсe #XX -- [ Pg.351 ]




SEARCH



Ion-exchange Modification of Zeolite LTA

Modification of FAU Zeolite through Ion-exchange

© 2024 chempedia.info