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Chromatography filtration

Regarding the color, we only see a need for colorless ionic liquids in very specific applications (see above). One easy treatment that often reduces coloration quite impressively, especially of imidazolium ionic liquids, is purification by column chromatography/filtration over silica 60. For this purification method, the ionic liquid is dissolved in a volatile solvent such as CFF2C12. Usually, most of the colored impurities stick to the silica, while the ionic liquid is eluted with the solvent. By repetition of the process several times, a seriously colored ionic liquid can be converted into an almost completely colorless material. [Pg.28]

Porous media are a part of many chemical processing applications, including reaction engineering, chromatography, filtration, separations, catalysis, and more. They also impact related processes the production of raw materials (hydrocarbons) from porous rock and the transport of chemical contaminants spilled into the environment. [Pg.2391]

Gel permeation chromatography, exclusion chromatography. gel filtration chromatography. A technique for separating the components of a mixture according to molecular volume differences. A porous solid phase (a polymer, molecular sieve) is used which can physically entrap small molecules in the pores whilst large molecules pass down the column more rapidly. A solvent pressure up to 1000 psi may be used. [Pg.98]

Sephadex A trade name for an insoluble hydrophilic substance prepared by cross-linking dextran, and used in gel filtration. It can also be linked to acidic or basic groups for ion exchange or to alkanes for the chromatography of lipophilic compounds. [Pg.356]

With Stirring, hydrazine hydrate (4 ml in 30 ml of THh ) was added over 60 min. The reaction mixture was then cooled to room temperature and filtered through Celite. The filtrate was concentrated in vacuo and the residue purified by chromatography through silica gel using 10% ether in hexane for elution. The fractions containing product were combined and evaporated to give the product as a clear oil (2.94g, 50%). [Pg.10]

A mixture of l-(r-Boc)indol-2-yl-tri- -butylstannanc (1.2 mmol) and 4-bromo-benzonitrile (1.0 mmol) and Pd(PPh3)2C , (0.02 mmol) in dry dioxane (5 ml) was heated at I00°C overnight under nitrogen. The reaction mixture was cooled, diluted with EtOAc and stirred for 15 min with 15% aq. KF. The precipitate was removed by filtration and washed with EtOAc. The EtOAc layer was separated, washed with brine, dried (Na2S04) and concentrated. The residue was purified by chromatography on silica. The yield was 66%. [Pg.100]

Gel filtration chromatography (GFC) is the name used to describe this method of separation in the biochemical literature. Under this heading, the method is primarily applied to aqueous solutions of solutes of biological origin. [Pg.642]

Lipoproteins may denature on heating and if present during pasteurization can result in the formation of haze or turbidity in the final product. This material was removed traditionally by filtration through asbestos (qv) sheets (6) however, health hazards associated with asbestos have led to its replacement by alternative filter materials (23,37,193). These media have been less effective than asbestos and further measures have been required to ensure the visual clarity of albumin products, eg, further filtration developments for Hpid removal (194), preferential denaturation of contaminants using in-process heat treatment, and anion-exchange chromatography (49). [Pg.533]

Finally, the techniques of nmr, infrared spectroscopy, and thin-layer chromatography also can be used to assay maleic anhydride (172). The individual anhydrides may be analyzed by gas chromatography (173,174). The isomeric acids can be determined by polarography (175), thermal analysis (176), paper and thin-layer chromatographies (177), and nonaqueous titrations with an alkaU (178). Maleic and fumaric acids may be separated by both gel filtration (179) and ion-exchange techniques (180). [Pg.459]

Polyethers are usually found in both the filtrate and the mycelial fraction, but in high yielding fermentations they are mosdy in the mycelium because of their low water-solubiUty (162). The high lipophilicity of both the free acid and the salt forms of the polyether antibiotics lends these compounds to efficient organic solvent extraction and chromatography (qv) on adsorbents such as siUca gel and alumina. Many of the production procedures utilize the separation of the mycelium followed by extraction using solvents such as methanol or acetone. A number of the polyethers can be readily crystallized, either as the free acid or as the sodium or potassium salt, after only minimal purification. [Pg.171]

In the development of new products, optimization of the fermentation medium for titer only often ignores the consequences of the medium properties on subsequent downstream processing steps such as filtration and chromatography. It is imperative, therefore, that there be effective communication and understanding between workers on the upstream and downstream phases of the produc t development if rational trade-offs are to be made to ensure overall optimahty of the process. One example is to make the conscious decision, in collaboration with those responsible for the downstream operations, whether to produce a protein in an unfolded form or in its native folded form the purification of the aggregated unfolded proteins is simpler than that of the native protein, but the refolding process itself to obtain the product in its final form may lack scalabihty. [Pg.2057]


See other pages where Chromatography filtration is mentioned: [Pg.2058]    [Pg.76]    [Pg.224]    [Pg.83]    [Pg.1816]    [Pg.245]    [Pg.2231]    [Pg.483]    [Pg.1646]    [Pg.2215]    [Pg.2062]    [Pg.416]    [Pg.148]    [Pg.32]    [Pg.2058]    [Pg.76]    [Pg.224]    [Pg.83]    [Pg.1816]    [Pg.245]    [Pg.2231]    [Pg.483]    [Pg.1646]    [Pg.2215]    [Pg.2062]    [Pg.416]    [Pg.148]    [Pg.32]    [Pg.157]    [Pg.10]    [Pg.112]    [Pg.128]    [Pg.215]    [Pg.331]    [Pg.43]    [Pg.44]    [Pg.47]    [Pg.49]    [Pg.50]    [Pg.530]    [Pg.532]    [Pg.339]    [Pg.298]    [Pg.241]    [Pg.343]    [Pg.341]    [Pg.357]    [Pg.104]    [Pg.2064]   
See also in sourсe #XX -- [ Pg.742 , Pg.755 ]

See also in sourсe #XX -- [ Pg.742 , Pg.755 ]

See also in sourсe #XX -- [ Pg.742 , Pg.755 ]

See also in sourсe #XX -- [ Pg.129 ]




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