Big Chemical Encyclopedia

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

Articles Figures Tables About

Resins gel type

Anion exchange resins—gel type — Strongly basic- —quaternary ammonium functionality... [Pg.1110]

Anion exchange resin-gel type— intermediate basicity... [Pg.1110]

Anion exchange resins- —gel type—weakly basic—polyamine functionality ... [Pg.1111]

Polymer-based, synthetic ion-exchangers known as resins are available commercially in gel type or truly porous forms. Gel-type resins are not porous in the usual sense of the word, since their structure depends upon swelhng in the solvent in which they are immersed. Removal of the solvent usually results in a collapse of the three-dimensional structure, and no significant surface area or pore diameter can be defined by the ordinaiy techniques available for truly porous materials. In their swollen state, gel-type resins approximate a true molecular-scale solution. Thus, we can identify an internal porosity p only in terms of the equilibrium uptake of water or other liquid. When crosslinked polymers are used as the support matrix, the internal porosity so defined varies in inverse proportion to the degree of crosslinkiug, with swelhng and therefore porosity typically being more... [Pg.1500]

Truly porous, synthetic ion exchangers are also available. These materials retain their porosity even after removal of the solvent and have measurable surface areas and pore size. The term macroreticular is commonly used for resins prepared from a phase separation technique, where the polymer matrix is prepared with the addition of a hq-uid that is a good solvent for the monomers, but in which the polymer is insoluble. Matrices prepared in this way usually have the appearance of a conglomerate of gel-type microspheres held together to... [Pg.1500]

For particles that have no macropores, such as gel-type ion-exchange resins, or when the solute holdup in the pore fluid is small, 0 may Be... [Pg.1513]

CFPs are normally manufactured as submillimetric beads or powders (Figure 2) [15]. A convenient simplified comparison between the micrometer and nanometer scale morphology of gel-type and macroreticular resins is illustrated in Figure 3. [Pg.201]

Figure 3. Schematic representation of the micro- and nanoscale morphology of gel-type (a) and macroreticular (b) resins [13], Level 1 is the representation of the dry materials. Level 2 is the representation of the microporous swollen materials at the same linear scale swelling involves the whole polymeric mass in the gel-type resin (2a) and the macropore walls in the macroreticular resin (2b). The morphology of the swollen polymer mass is similar in both gel-type and macroreticular resins (3a,b). Nanopores are actually formed by the void space surrounding the polymeric chains, as shown in level 4, and are a few nanometer wide. (Reprinted from Ref [12], 2003, with permission from Elsevier.)... Figure 3. Schematic representation of the micro- and nanoscale morphology of gel-type (a) and macroreticular (b) resins [13], Level 1 is the representation of the dry materials. Level 2 is the representation of the microporous swollen materials at the same linear scale swelling involves the whole polymeric mass in the gel-type resin (2a) and the macropore walls in the macroreticular resin (2b). The morphology of the swollen polymer mass is similar in both gel-type and macroreticular resins (3a,b). Nanopores are actually formed by the void space surrounding the polymeric chains, as shown in level 4, and are a few nanometer wide. (Reprinted from Ref [12], 2003, with permission from Elsevier.)...
CFPs, especially the macroreticular ones, suffer of an appreciable fragility and require considerable attention to mechanical stress when employed in slurry reactors. A case history has been evaluated in this connection [29] and a considerable stability to friction in the case of some Pd / gel-type resin catalysts has been recorded (Figure 8). In any case, it has been observed that a shaken reactor is by far preferable to any rotationally stirred ones [29]. [Pg.206]

Synthesis (TCS). The very same term was independently proporsed by Corain and associates for the size controlled synthesis of palladium nanoparticles in 2004 [68]. In a number of cases they observed that palladium nanoclusters, supported on gel-type resins of different nature and obtained with the RIMP method, exhibited a remarkable agreement between the size of the cavities of swollen supports (as assessed by means of ISEC, see Section 4) and the diameter of the metal nanoclusters (Table 4, Entries 1-3) [10,11,66,71,72,87]. [Pg.215]

The reduction of palladium(II) with an alcoholic solution of NaBH4 [101] or by treatment in situ of the methanol-swollen material under hydrogen [129] yielded a supported palladium catalyst, referred to as self supported by the authors [101,129]. The same co-polymerization reaction was carried out inside the nanopores of a DMF-swollen gel-type resin made by DMA and MBAA (crosslinker, 4% mol) [101,129], thus obtaining a sequential IPN [131]. Also this material was transformed into a... [Pg.216]

The first project [9] dealt with the evaluation of the effect of cross-linking degree (c.l.d.) in a series of five gel-type resins, on the diameter of Pd° nanoclusters obtained upon reducing resin-bound Pd centres. In this project c.l.d. was let to range from 1 to 9% mol (Figure 3). [Pg.413]

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 resins can be divided into two groups having major structural differences gel and macroreticular . In the case of gel type resins if the beads are totally dry, then the polymeric matrix collapses and the polystyrene chains will be as close as atomic forces allow. Therefore, swelling ability of the reactants is a prerequisite for catalysis by gel resins. Gel resins are characterized by a divinyl benzene content that is generally below 12%. [Pg.127]

One of the most remarkable attributes of Pechini-type routines is the behaviour of precursor resins (gels) upon heating. On the first stage of thermal decomposition of samples, being dried at approx. 120°C, they decompose forming very porous and voluminous sponge-cake-like materials [6], Probably, just at this temperature, a highly porous intermediate is... [Pg.505]

Resins with a DVB content of less than 8 wt.% are of the gel-type without permanent porosity. Such resins function only in the presence of polar components that swell the resin structure. Resins with a DVB content of 12 wt.% or more have permanent macroporosity. These materials also have a microporous gel phase consisting of gel-type microspheres [25],... [Pg.213]


See other pages where Resins gel type is mentioned: [Pg.1112]    [Pg.373]    [Pg.380]    [Pg.1496]    [Pg.1501]    [Pg.374]    [Pg.188]    [Pg.200]    [Pg.200]    [Pg.327]    [Pg.202]    [Pg.214]    [Pg.215]    [Pg.218]    [Pg.220]    [Pg.220]    [Pg.221]    [Pg.227]    [Pg.6]    [Pg.4]    [Pg.9]    [Pg.22]    [Pg.54]    [Pg.1381]    [Pg.1456]    [Pg.1458]    [Pg.229]   
See also in sourсe #XX -- [ Pg.3 ]

See also in sourсe #XX -- [ Pg.59 ]

See also in sourсe #XX -- [ Pg.37 ]




SEARCH



Resins types

© 2024 chempedia.info