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Mixed sorbent layers

Mixed sorbent layers have been used by various workers to increase resolution of certain samples compared to that obtained on the separate phases. Binary layers that have been reported include silica gel-alumina, kieselguhr-alumina, alumina-calcium sulfate, magnesia-lcieselguhr, cellulose-silica gel, polyamide-silica gel, polyamide-kieselguhr, polyamide-cellulose, and polyamide-glass powder. The properties of these mixed layers are somewhere between those of the two separate phases but are impossible to predict or explain with certainty. Applications of mixed layers are contained in the older standard TLC texts and reviews. [Pg.17]

Minocycline, 468-473 Mixed sorbent layers, 17 Mixture design statistical method of optimization, 88-91... [Pg.1097]

For this technique, the upper plate has a mobile phase inlet channel on one edge and a slit at the opposite edge for directing the mobile phase toward the next plate (33). The slit (width approx. 0.1 mm) can be produced by cutting the layers with a sharp blade this enables easy passage of mobile phase and separated compounds without any mixing. The cushion of the OPLC instrument is applied to the uppermost layer only, and each plate presses on to the sorbent layer below. [Pg.189]

Some prepared layers are available that are mixed sorbent plates. Sometimes, the mixture is to allow multiple modes of chromatography to be used at once or in sequence. Other times, the mixture has been chosen to improve the separation characteristics or to aid in holding the active sorbent onto the support. This latter is often the reason cellulose is part of the layer formulation. [Pg.32]

Anionic surfactants are present in surface water, resulting in serious environmental pollution. Therefore, adsorption of surfactants, such as sodium dodecylsulfate [155,156], on Mg/Al LDHs has received considerable attention. Ulibarri et al. also published the results of sorption of an anionic surfactant (sodium dodecylbenzenesulfonate) from water by LDHs and calcined samples (773 K), focusing both on their potential application as a sorbent and on the possibility of their recycling [154,157]. They found that anionic exchange was complete when the interlayer anion in the LDH precursor was Cl", reaching 100 % of AEG, and calcined LDH-carbonates were better adsorbents than those derived from LDH-chloride samples, however. It was also claimed that an increase in the crystallinity of the LDH samples probably leads to better ordered calcined mixed oxides, facilitating reconstruction of the layers and enlarging the absorption capacity. [Pg.206]

Besides the above differentiation, restricted-access media can be further subdivided on the basis of the topochemistry of the bonded phase. Packings with a uniform surface topochemistry show a homogenous ligand coverage, whereas packings with a dual topochemistry show a different chemical modification of the pore internal surface and the particle external surface (114). Restricted-access media of the former type are divided into mixed-mode and mixed-function phases, bonded-micellar phases, biomatrix, binary-layered phases, shielded hydrophobic phases, and polymer-coated mixed-function phases. Restricted-access media of the latter type include the Pinkerton s internal surface reversed-phase, Haginaka s internal surface reversed-phase diol, alkyl-diol silica, Kimata s restricted-access media, dual-zone phase, tris-modified Styrosorb, Svec s restricted-access media, diphil sorbents, Ultrabiosep phases. Bio Trap phases, and semipermeable surface phases. [Pg.607]

A variety of sorbents have been used as the stationary phase in TLC, including silica gel, cellulose, alumina, polyamides, ion exchangers, chemically modified silica gel, and mixed layers of two or more materials, coated on a suitable support. Currently in the pharmaceutical industry, commercially precoated high-performance TLC (HPTLC) plates with fine particle layers are commonly used for fast, efficient, and reproducible separations. The choices of mobile phase range from single component solvent systems to multiple-component solvent systems with the latter being most common. The majority of TLC applications are normal phase, which is also a complementary feature to HPLC that uses mostly reverse-phase columns. [Pg.204]

Among the stationary phases for modern liquid chromatography one should mention multiphase sorbents. It is clear that the adsorptional properties of such sorbents are closely related to the uniformity of mixing of bonded molecules in a bonded layer. [Pg.210]

Hexane was used to extract milk and juice samples and sonication was used to mix the samples. The hexane layer was separated and passed through a silica-gel column. Bread and vegetable samples were pulverized and extracted with hexane then cleaned in a silica-gel sorbent. [Pg.235]

Raisglid, M. and Burke, M. F. 1997. Solid phase extraction using layered, mixed and single sorbent phases, Pittsburg Conference Abstract number 653, Atlanta, Georgia. [Pg.330]

Over the past decade there have been a number of further significant improvements in the technique. For instance, there are now a wide range of sorbents available in the form of pre-coated plates and the applicability of the technique has also been extended with the increasing range of bonded phase sorbents, e.g. reverse phases (Cg and Cig), those of medium-polarity (amino and cyano) and other specialised layers featuring chiral and mixed stationary phases. [Pg.44]

SORPTION. A general term for the attraction between a layer and a solute, without specification of the type of physical mechanism (i.e., adsorption, partition, ion exchange) or mixed mechanism involved. Sorbent is a related general term referring to the layer itself. [Pg.484]

Particularly in the beginning of thin-layer chromatography, but also today, sorbents without chemically modified surfaces are of most importance. In former times hand-made thin-layer plates were used nearly exclusively, but today the trend has moved in the direction of industrial precoated layers. In addition to glass plates, plastic and aluminium sheets are also offered as supports for the precoated layers. To stabilize the precoated layers mechanically, special binders are added that do not or nearly do not interfere with the chromatographic properties. To enlarge the possibilities of detection, added indicators can be mixed homogeneously with sorbents. Different types of silica gel are by far the most versatile and therefore the most frequently used stationary phases in the case of bulk sorbents as well as for application to precoated layers. [Pg.102]


See other pages where Mixed sorbent layers is mentioned: [Pg.852]    [Pg.518]    [Pg.518]    [Pg.305]    [Pg.419]    [Pg.66]    [Pg.1149]    [Pg.22]    [Pg.20]    [Pg.346]    [Pg.748]    [Pg.856]    [Pg.690]    [Pg.313]    [Pg.106]    [Pg.484]    [Pg.37]    [Pg.255]    [Pg.1077]    [Pg.313]    [Pg.398]    [Pg.562]    [Pg.1058]    [Pg.392]    [Pg.313]    [Pg.398]    [Pg.562]    [Pg.1058]   
See also in sourсe #XX -- [ Pg.17 ]




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