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Column tailing

The other end is called the tail (lower pressure). If the mobile phase is the lighter (upper) liquid, it should be flown entering the CCC column tail side and exiting from the head side. If the mobile phase is the denser and lower liquid phase, it should be flown in the head-to-tail direction [1]. [Pg.216]

Liquid benzine containing plastic residues Distillation. The plastic residues recovered from the distillation column tailings are treated as a waste product. [Pg.62]

The t-values in this table are for a two-tailed test. For a one-tailed test, the a values for each column are half of the stated value, column for a one-tailed test is for the 95% confidence level, a = 0.05. For example, the first... [Pg.726]

Figure 2 illustrates the three-step MIBK process employed by Hibernia Scholven (83). This process is designed to permit the intermediate recovery of refined diacetone alcohol and mesityl oxide. In the first step acetone and dilute sodium hydroxide are fed continuously to a reactor at low temperature and with a reactor residence time of approximately one hour. The product is then stabilized with phosphoric acid and stripped of unreacted acetone to yield a cmde diacetone alcohol stream. More phosphoric acid is then added, and the diacetone alcohol dehydrated to mesityl oxide in a distillation column. Mesityl oxide is recovered overhead in this column and fed to a further distillation column where residual acetone is removed and recycled to yield a tails stream containing 98—99% mesityl oxide. The mesityl oxide is then hydrogenated to MIBK in a reactive distillation conducted at atmospheric pressure and 110°C. Simultaneous hydrogenation and rectification are achieved in a column fitted with a palladium catalyst bed, and yields of mesityl oxide to MIBK exceeding 96% are obtained. [Pg.491]

Cehte or firebrick packing for glc columns is often treated with TMCS, DMCS, or other volatile silylating agents (see Table 1) to reduce tailing by polar organic compounds. A chemically bonded methyl siUcone support is stable for temperature programming to 390°C and allows elution of hydrocarbons up to C q (20). [Pg.72]

The carbon monoxide purity from the Cosorb process is very high because physically absorbed gases are removed from the solution prior to the low pressure stripping column. Furthermore, there is no potential for oxidation of absorbed carbon monoxide as ia the copper—Hquor process. These two factors lead to the production of very high purity carbon monoxide, 99+ %. Feed impurities exit with the hydrogen-rich tail gas therefore, the purity of this coproduct hydrogen stream depends on the impurity level ia the feed gas. [Pg.58]

Similarly, small (0.2—0.6 mm) air bubbles are introduced into a 2.6-m Deister Flotaire column at an intermediate level allowing rapid flotation of readily floatable material in the upper recovery zone. The bottom air permits longer retention time of the harder-to-float particles in the presence of micrometer-sized bubbles at a reduced downward velocity. The first commercial unit went on stream in 1986. It was used to improve the recovery of <0.6 mm (—28 mesh) coal in the plant s tailings. An average of 5.5% increase in coal recovery resulted from its use (14). The second commercial use processed <0.15 mm (—100 mesh) coal feed. [Pg.255]

The assay of ethyleneamines is usually done by gas chromatography. Compared to packed columns, in which severe tailing is often encountered due to the high polarity of the ethyleneamines, capillary columns provide better component separation and quantification. Typically, amines can be analyzed using fused siUca capillary columns with dimethyl silicones, substituted dimethyl silicones or PEG Compound 20 M as the stationary phase (150). [Pg.45]

The structure formation in an ER fluid was simulated [99]. The characteristic parameter is the ratio of the Brownian force to the dipolar force. Over a wide range of this ratio there is rapid chain formation followed by aggregation of chains into thick columns with a body-centered tetragonal structure observed. Above a threshold of the intensity of an external ahgn-ing field, condensation of the particles happens [100]. This effect has also been studied for MR fluids [101]. The rheological behavior of ER fluids [102] depends on the structure formed chainlike, shear-string, or liquid. Coexistence in dipolar fluids in a field [103], for a Stockmayer fluid in an applied field [104], and the structure of soft-sphere dipolar fluids were investigated [105], and ferroelectric phases were found [106]. An island of vapor-liquid coexistence was found for dipolar hard spherocylinders [107]. It exists between a phase where the particles form chains of dipoles in a nose-to-tail... [Pg.764]

Tailing peaks or longer than expected elution volumes are sometimes caused by low solubility of the protein in the mobile phase. Using a trial-and-error process, select the proper pFf and ionic strength to address this problem. Detergents such as sodium dodecyl sulfate (SDS) are sometimes helpful but, because they change the conformation of many proteins and are difficult to remove from the column should be used only if other methods fail. [Pg.90]

The use of hexafluoroisopropanol (HFIP) as an SEC eluent has become popular for the analysis of polyesters and polyamides. Conventional PS/DVB-based SEC columns have been widely used for HFIP applications, although the relatively high polarity of HFIP has led to some practical difficulties (1) the SEC calibration curve can exhibit excessive curvature, (2) polydisperse samples can exhibit dislocations or shoulders on the peaks, and (3) low molecular weight resolution can be lost, causing additive/system peaks to coelute with the low molecular weight tail of the polymer distribution... [Pg.359]

PVP K-15 and K-30 peaks are symmetric in water and water/methanol, except for the TSK GM-PWxl column in water. This suggests an interaction between PVP K-15 and K-30 with the TSK GM-PWxl column in water. System peaks overlap with the low molecular weight tails of the PVP K-15 and K-30 peaks for all four columns in water. In water/methanol the separation of the system peaks from the polymer peaks is much better for all four columns. [Pg.519]

Am columns. However, for typical polyethylenes produced using Ziegler-Natta catalysts, which do not have a high molecular weight tail, shear degradation was not a concern. [Pg.589]


See other pages where Column tailing is mentioned: [Pg.328]    [Pg.156]    [Pg.328]    [Pg.156]    [Pg.1117]    [Pg.555]    [Pg.609]    [Pg.85]    [Pg.241]    [Pg.503]    [Pg.491]    [Pg.43]    [Pg.43]    [Pg.44]    [Pg.199]    [Pg.212]    [Pg.85]    [Pg.100]    [Pg.1533]    [Pg.447]    [Pg.176]    [Pg.109]    [Pg.231]    [Pg.428]    [Pg.99]    [Pg.65]    [Pg.169]    [Pg.435]    [Pg.439]    [Pg.524]    [Pg.544]    [Pg.573]    [Pg.409]    [Pg.93]    [Pg.129]    [Pg.318]    [Pg.506]    [Pg.7]   
See also in sourсe #XX -- [ Pg.34 ]




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