Fractional separation

Fractionation separates fines and short, weak cellulose fibers from longer, stronger cellulose fibers (52). Its primary appHcation is ia processiag old cormgated coataiaers iato aew packagiag products. 

In the wood rosin process, rosin is isolated from aged pine stumps that have been left in fields cleared for farming or lumbering operations. The stumps are cut and shredded to pieces the size of matchsticks. The wood chips are then extracted with an appropriate solvent, eg, aUphatic or aromatic petroleum hydrocarbons or ketones. The extract is fractionally separated into nonvolatile cmde rosin, volatile extractibles, and recovered solvent. The dark rosin is usually refined further to lighter-colored products using selective solvents or absorption. 

However, for the past 30 years fractional separation has been the basis for most asphalt composition analysis (Fig. 10). The separation methods that have been used divide asphalt into operationally defined fractions. Four types of asphalt separation procedures are now in use ( /) chemical precipitation in which / -pentane separation of asphaltenes is foUowed by chemical precipitation of other fractions with sulfuric acid of increasing concentration (ASTM D2006) (2) solvent fractionation separation of an "asphaltene" fraction by the use of 1-butanol foUowed by dissolution of the 1-butanol solubles in... 

The fractions obtained in these schemes are defined operationally or proceduraHy. The amount and type of asphaltenes in an asphalt are, for instance, defined by the solvent used for precipitating them. Fractional separation of asphalt does not provide well-defined chemical components. The materials separated should only be defined in terms of the particular test procedure. 

Distillation. Most fatty acids are distilled to produce high quaHty products having exceUent color and a low level of impurities. Distillation removes odor bodies and low boiling unsaponifiable material in a light ends or heads fraction, and higher boiling material such as polymerized material, triglycerides, color bodies, and heavy decomposition products are removed as a bottoms or pitch fraction. The middle fractions sometimes can be used as is, or they can be fractionated (separated) into relatively pure materials such as lauric, myristic, palmitic, and stearic acids. 

FIGURE 16.7 Native starch ( ) and fractions of native starch differing in their branching characteristics (nb/lcb amylose -type fraction scb amylopectin -t/pe fraction ) separated on semipreparative... 

Each of the four columns was packed with CPG00120C d = 13.0 nm). The column dimensions and experimental conditions are listed in Table 23.1. The flow rates (solution and solvent) were set to be proportional to the cross section of the column, whenever possible. The number of drops collected in each test tube was almost proportional to the cross section, especially for the initial fractions that might show a shift in M. Figure 23.9 shows chromatograms for some the fractions separated using 2.1-, 3.9-, and 7.8-mm i.d. columns. The result with the 7.8-mm i.d. column is a reproduction of Fig. 23.2 (3). Chromatograms of the fractions obtained from the 1.0-mm i.d. column overlapped with the chromatogram of the injected polymer sample (not shown). 

Petroleum distillation, (a) A distillation tower at a petroleum refinery, (b) A diagram showing the boiling points of the petroleum fractions separated by distillation. 

A gas chromatographic method is described in this work for the analysis of tetradecane-l,4-sultone (C14 5-sultone) and the combination of 2-chloro-tetradecane-l,3-sultone (C14 2-chloro-y-sultone) and l-tetradecene-l,3-sultone (C14 unsaturated y-sultone) in neutral oils isolated from alkenesulfonate. Samples of the neutral oil are diluted in hexane and injected directly into the gas chromatograph. Quantitative data are obtained by comparison to known amounts of the respective sultones. Through the use of silica gel column chromatography followed by GC of collected fractions, separation and individual quantitation of the 2-chlorotetradecane-l,3-sultone and l-tetradecene-l,3-sultone can be obtained. 

A PVC-poor light fraction separated from mixed plastic household waste was pyrolysed to yield aromatic oils and heat-providing gas. Target products were benzene, toluene, xylenes, and styrene. Problematic pollutants were... 

Ghiselli, A. et al.. Antioxidant activity of different phenolic fractions separated from an Italian red wine, J. Agric. Food Chem., 46, 361, 1998. 

Baker, R.A. 1979. Clarifying properties of pectin fractions separated by ester... 

Fig. 128.—Calculated distribution for each of eight fractions separated from the initial distribution shown by the uppermost curve. Dotted lines represent distribution of polymer remaining in the dilute phase after each successive precipitation with =10 in each case. The distribution for each fraction, obtained as the differences between successive dotted curves, is shown by a solid curve. (Schulz. )...

Preparative TLC may be applied to cleanup selected compound fractions separated from geochemical samples by such methods as HPLC, as Aries et al. [113] has described. To analyze phospholipids and nonphospholipids in sediments, organic matter was extracted and extracts LC-fractionated to obtain polar fractions. At the... 

Table VIII. The effect of three fractions separated from extracts of tall fescue (pH 5.5) ...

Fractionations. Following lyophilization of the polar leachate fractions, separations by exclusion chromatography suggest three major molecular weight regions, labelled peak 1A, peak 1B and peak 2 (Figure 3). Retention times on a G—15 Sephadex gel indicate molecular weights of peaks 1A and 1B compounds to be between 600 and 1000. 

Fractional separation of tin compounds used as stabilisers in PVC was based on substoichiometric isotope dilution analysis [446]. The tin compounds were isolated by extraction and complexed with salicylideneamino-2-thiophenol, followed by controlled addition of y-irradiated tributyl tin oxide and measurement of the y-activity. PVC containing a nominal 0.63% (Bu Sn analysed 0.614 0.016% in nine determinations. 

Supercritical C02 extraction coupled with a fractional separation technique is used by producers of flavours and fragrances to separate and purify volatile flavour and fragrance concentrates. Like any solvent, supercritical C02, it allows processing chemicals by predpita-tion or recrystallisation, obtaining partides of controlled size and shape, without excessive fines without thermal stresses and controlling the shape of a polymorphic substance. 

FIGURE 13.4 Total ion chromatograms from the ID LC/MS analysis of a yeast ribosomal protein fraction separated using 0.1% TFA (Panel a) and 0.1% formic acid (Panel b) as mobile phase modifiers. TFA produced narrower, more concentrated, peaks for mass analysis that did not overcome the significant electrospray ionization suppression associated with using this modifier for LC/MS studies, resulting in an overall reduction in component intensities. 

TABLE I. Structural Characteristics of Coal Fractions Separated from Solubilized... 

Fig. 9. Pulse microreactor system for use with 13C-labeled hydrocarbons. D, E, and J are microreactors J contains the catalyst to be used for hydrocarbon skeletal reaction D and E are used, when necessary, to generate the required reactant hydrocarbon from a non-hydrocarbon precursor (e.g., alcohol dehydration in D and olefin hydrogenation in E) reactant injected at C. F is a trap which allows the accumulation of products from several reaction pulses before analysis G is a G.P.C. column, K a katharometer. Traps H collect fractions separated on G for subsequent mass spectrometric study. When generating reactant hydrocarbon in D and E, a two-step process is preferable in which, with J below reaction temperature, the purified reactant hydrocarbon is collected in H, and this is recycled as reactant with D and E below reaction temperature but with J at reaction temperature. After C. Corolleur, S. Corolleur, and F. G. Gault, J. Catal. 24, 385 (1972).

The air classification method separates dry solid particles according to weight and/or size by suspension in and settling from an air stream of appropriate velocity. Centrifugal fractionation separates particles suspended in a so-... 

Michael, G. Al-Siri, M. Khan, Z. H., and Ah, F. A., Differences in Average Chemical Structures of Asphaltene Fractions Separated From Feed and Product Oils of a Mild Thermal Processing Reaction. Energy Fuels, 2005. 19 pp. 1598-1605. 

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