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Test mixtures

FIG. 14-24 Performance of two crossflow plates operating at 0.13 bar pressure and total reflux. Test mixture etbylbenzene/styrene. Spacing between plates is 0.50 m, and outlet weir height is 38 mm. Ut = superficial vapor velocity, pc = vapor density. [Billet, Comad, and Giuhh, I. Chem. E. Symp. Ser. No. 32, 5, 111 (1969).]... [Pg.1373]

Efficiency data for a representative structured packing at two column diameters are shown in Fig. 14-74. The Max-Pak packing has a surface area of 246 m /m (7.5 ft /fE). The same test mixture (cyclo-hexane//i-heptane) and operating pressure was used for both tests. It would appear that column diameter does not have an influence in this range of values (0.43 to 1.2 m). [Pg.1400]

Efficiency and pressure drop data for Siilzer BX metal gauze structured packing and for three test mixtures are shown in Fig. 14-7.5. For the ethyl benzene/styrene test mixture, the effect of operating pressure is shown. The high viscosity mixture, propylene glycoL/ethylene... [Pg.1400]

A list of danger categories is given in Table 14.2. Note that chemicals may possess several hazards, e.g. nitric acid is classed as both an oxidizer and a conosive. If a chemical is not in one of these categories it is not generally considered to be dangerous. If the hazards of a new chemical have not been established it should be labelled Caution - substance not yet fully tested . Mixtures can be classified either from results from tests on the preparation, or by calculation to predict the healtli effects of the product based on the properties of individual components and tlieu concentration in the mixture. Preparations need to be classified for both physico-chemical and health effects but, to date, not for environmental effects. [Pg.443]

MESG is defined in terms of die precise test mediod and apparatus used, of which there are three variants British, lEC, and Underwriters Laboratories, Inc. Each apparatus consists of two combusdon chambers connected by a slot of specified size and variable widdi. The separate chambers are filled with the test mixture. The MESG is die maximum slot widdi that prevents flame propagadoii between die chambers for all composi-doiis of die test gas in air under the specified test coiididoiis. Phillips (1987) describes and compares diese three types of experimental apparatus for determining the MESG. [Pg.100]

Stable Detonation A detonation that progresses through a confined system without significant variadon of velocity and pressure character-isdcs. Eor atmospheric condidons, typical velocides range between 1600 and 2200 m/s for standard test mixtures and test procedures. [Pg.206]

FIGURE 7.2 (A) Separation of a standard protein mixture. A test mixture consisting of BSA... [Pg.223]

S mg), dimer (peak I) and monomer (peak 2), ovalbumin (S mg) (peak 3), and cytochrome c (3 mg) (peak 4) was loaded onto a Fractogel EMD BioSEC column (600 X 16 mm) with a bed height of 600 mm. PBS (pH 7.2) was used as the eluent at a flow rate of I ml/min the sample volume was O.S ml. (B) The same protein sample as in A was injected onto a column of identical dimensions packed with unmodified Fractogel HW 6S. Without the tentacle modification the base matrix displays only a poor resolution of the test mixture. [Pg.223]

Figure 15.11 (a) Total ion clnomatogram of a Grob test mixture obtained on an Rtx-1701 column, and (b) re-injection of the entire clnomatogram on to an Rtx-5 column. Peak identification is as follows a, 2,3-butanediol b, decane c, undecane d, 1-octanol e, nonanal f, 2,6-dimethylphenol g, 2-ethylhexanoic acid h, 2,6-dimethylaniline i, decanoic acid methyl ester ], dicyclohexylamine k, undecanoic acid, methyl ester 1, dodecanoic acid, methyl ester. Adapted from Journal of High Resolution Chromatography, 21, M. J. Tomlinson and C. L. Wilkins, Evaluation of a semi-automated multidimensional gas chromatography-infrared-mass specti ometry system for initant analysis , pp. 347-354, 1998, with permission from Wiley-VCH. [Pg.424]

Recovery 93% from amino acid test mixture. b Recovery 100.6% from amino acid test mixture. e Recovery 99.2% from amino acid test mixture. d Decarboxylase-CO method (108, 106). [Pg.20]

The preparations of luciferin (Ln, an electron acceptor) and soluble enzyme used were crude or only partially purified. The luciferase was an insoluble particulate material, possibly composed of many substances having various functions. Moreover, the luciferin-luciferase reaction was negative when both luciferin and luciferase were prepared from certain species of luminous fungus. It appears that the light production reported was the result of a complex mechanism involving unknown substances in the test mixture, and probably the crucial step of the light-emitting reaction is not represented by the above schemes. [Pg.270]

The injector temperature should be determined by the nature of the sample and the volume injected, not by the column temperature. When analyzing biological or high-boiling samples, clean the injector body with methanol or other suitable solvent once per week. Install a clean packed injector liner and a new septum, preferably near the end of a workday. Program the column to its maximum temperature, then cool the column and run a test mixture to check the system using standard conditions. [Pg.174]

Their reaction was tested on the individual components of the test mixture indole, ergotamine tartrate, ergotaminine and ergobasine [ergometrine) [3]. The results obtained were as follows ... [Pg.228]

Figure 9. Observed increases in mouse assay toxicity of test mixtures of shellfish meat and toxin Cl (4), hydrolyzed with varying concentrations of HCI acid. Two series of experiments are shown. The initial concentration of toxin Cl was uniform for all samples in a series. Toxicity is expressed on the vertical axis as percentage of the maximum toxicity attained for that series. Figure 9. Observed increases in mouse assay toxicity of test mixtures of shellfish meat and toxin Cl (4), hydrolyzed with varying concentrations of HCI acid. Two series of experiments are shown. The initial concentration of toxin Cl was uniform for all samples in a series. Toxicity is expressed on the vertical axis as percentage of the maximum toxicity attained for that series.
Inteilaboratory study (30 lata) Analysis of test mixtures and/or matrices of known content of the analytes to be certified ... [Pg.97]

In practice, it is more difficult to optimize resolution as a function of the relative retentlvity than to optimize retention. Thus, unless the mixture is very complex or contains components that are particularly difficult to separate it may be possible to optimize a particular separation using the linear equation (1.72) as demonstrated by Bttre [177]. Figure 1.13 illustrates the relative change in peak position for a polarity test mixture with two identical, serially coupled open tubular columns, coated with a poly(dimethylslloxane) and Carbowax 20 M stationary phases, as a function of their relative retentlvity on the second column. The linear relationship predicted by equation (1.72) effectively predicts the relative peak positions and indicates that a nearly... [Pg.35]

Figure 2.7 Activity test of an uncoated fused silica capillary after deactivation with poly(phenyliaethylhydrosiloxane), (A), and before deactivation, (B). Precolunn 15 x 0.20 m I.D. coated with SE-54. Test columns 10 a x 0.20 I.D. The column tandem was programmed from 40 to I80 c at a C/min after a 1 min isothermal hold with a hydrogen carrier gas velocity of 50 cm/s. The test mixture contained 10 n-decane, Cg-NH = l-aminooctane, PY 3,5-dimethylpyrimidine, C 2 n-dodecane, - 1-amlnodecane, DMA ... Figure 2.7 Activity test of an uncoated fused silica capillary after deactivation with poly(phenyliaethylhydrosiloxane), (A), and before deactivation, (B). Precolunn 15 x 0.20 m I.D. coated with SE-54. Test columns 10 a x 0.20 I.D. The column tandem was programmed from 40 to I80 c at a C/min after a 1 min isothermal hold with a hydrogen carrier gas velocity of 50 cm/s. The test mixture contained 10 n-decane, Cg-NH = l-aminooctane, PY 3,5-dimethylpyrimidine, C 2 n-dodecane, - 1-amlnodecane, DMA ...
Inject the test mixture under conditions that allow ca. 2 ng of a single test substance to enter the column (e.g., 1 microliter with a split ratio of 1 20 to 1 50, depending on injector design). [Pg.87]

Figure 4.4 Separation of SRM 1647 and SRH 869 polycyclic aromatic hydrocarbon test mixtures on a monomeric and polymeric reversed-phase octadecylsiloxane bonded phases by gradient elution. (Reproduced with permission from ref. 69. Copyright American Chemical Society). Figure 4.4 Separation of SRM 1647 and SRH 869 polycyclic aromatic hydrocarbon test mixtures on a monomeric and polymeric reversed-phase octadecylsiloxane bonded phases by gradient elution. (Reproduced with permission from ref. 69. Copyright American Chemical Society).
Test mixture should contain components that correctly characterize the column in terms of both kinetic and thermodynamic performance. [Pg.184]

A value for the column dead volume is required in most calculations. It is convenient to have one cosponent of the test mixture as an unretained solute. [Pg.184]

At least two components of the test mixture should have k values between 2 and 10. [Pg.184]

Having chosen the test mixture and mobile diase composition, the chromatogram is run, usually at a fairly fast chart speed to reduce errors associated with the measurement of peak widths, etc.. Figure 4.10. The parameters calculated from the chromatogram are the retention volume and capacity factor of each component, the plate count for the unretained peak and at least one of the retained peaks, the peak asymmetry factor for each component, and the separation factor for at least one pair of solutes. The pressure drop for the column at the optimum test flow rate should also be noted. This data is then used to determine two types of performance criteria. These are kinetic parameters, which indicate how well the column is physically packed, and thermodynamic parameters, which indicate whether the column packing material meets the manufacturer s specifications. Examples of such thermodynamic parameters are whether the percentage oi bonded... [Pg.184]

Figure 4.10 Typical routine column test chromatogram for a 30 cm X 4.6 mm I. D. column pacXed with an octadecylsiloxane bonded silica packing of lO micrometers particle diameter. The test mixture consisted of resorcinol (0.55 mg/ml), acetophenone (0.025 mg/ml), naphthalene (0.20 mg/ml) and anthracene (0.01 mg/ml) in acetonitrile, 10 microliters injected. The separation was performed isocratically at 23 C with acetonitrile-water (55 45) as the mobile phase at a flow rate of 1.5 ml/min. Detection was by UV at 254 nm (0.1 AUFS). Figure 4.10 Typical routine column test chromatogram for a 30 cm X 4.6 mm I. D. column pacXed with an octadecylsiloxane bonded silica packing of lO micrometers particle diameter. The test mixture consisted of resorcinol (0.55 mg/ml), acetophenone (0.025 mg/ml), naphthalene (0.20 mg/ml) and anthracene (0.01 mg/ml) in acetonitrile, 10 microliters injected. The separation was performed isocratically at 23 C with acetonitrile-water (55 45) as the mobile phase at a flow rate of 1.5 ml/min. Detection was by UV at 254 nm (0.1 AUFS).
Figure 1.15 Fast analysis of a test mixture on a 10 cm x 4.6 mm I.D. column packed with 3 micrometer octa< ecylsilanized silica with a mobile phase flow rate of 3.4 mi. i.n (acetonitrile-water 7 3) and operating pressure of ca. 340 atmospheres. Peaks 1 uracil, 2 phenol, 3 - nitrobenzene, 4 - toluene, 5 -ethylbenzene, 6 - isopropylbenzene, and 7 - tert.-butylbenzene. (Reproduced with permission from ref. 222. Copyright Friedr. Vieweg 6 Sohn). Figure 1.15 Fast analysis of a test mixture on a 10 cm x 4.6 mm I.D. column packed with 3 micrometer octa< ecylsilanized silica with a mobile phase flow rate of 3.4 mi. i.n (acetonitrile-water 7 3) and operating pressure of ca. 340 atmospheres. Peaks 1 uracil, 2 phenol, 3 - nitrobenzene, 4 - toluene, 5 -ethylbenzene, 6 - isopropylbenzene, and 7 - tert.-butylbenzene. (Reproduced with permission from ref. 222. Copyright Friedr. Vieweg 6 Sohn).
Figure 1.16 Separation ot a test mixture by adsorption chromatography on a 1 m x 1 mm I.D. small bore column packed with 8 aicrometer Zorbax B.P. Sil operated at a flow rate of ISO microliters/min (left) and a 22 m x 1 mm I.D. column of the same packing material prepared by series coupling of 1 m segments and operated at a flow rate of 15 microliters/min (right). (Reproduced with permission from ref. 234. Copyright American Chemical Society). Figure 1.16 Separation ot a test mixture by adsorption chromatography on a 1 m x 1 mm I.D. small bore column packed with 8 aicrometer Zorbax B.P. Sil operated at a flow rate of ISO microliters/min (left) and a 22 m x 1 mm I.D. column of the same packing material prepared by series coupling of 1 m segments and operated at a flow rate of 15 microliters/min (right). (Reproduced with permission from ref. 234. Copyright American Chemical Society).
Figura 2.9 Dse of th Grob test Mixture to compare tbe activity of various glass surfaces coated with ov-ioi. Surface types A > Untreated pyrex glass, B pyrex glass deactivated by thermal degradation of Ceurbowax 20M, C < SCOT column, prepared with Silanox 101, D pyrex glass column coated with a layer of barium carbonate and deactivated as in (B), and E - untreated fused silica. Components are identified in Table 2.7 with ac - 2-ethylhexanoic acid. (Reproduced with permission from ref. 152. Copyright Elsevier Scientific Publishing Co.)... Figura 2.9 Dse of th Grob test Mixture to compare tbe activity of various glass surfaces coated with ov-ioi. Surface types A > Untreated pyrex glass, B pyrex glass deactivated by thermal degradation of Ceurbowax 20M, C < SCOT column, prepared with Silanox 101, D pyrex glass column coated with a layer of barium carbonate and deactivated as in (B), and E - untreated fused silica. Components are identified in Table 2.7 with ac - 2-ethylhexanoic acid. (Reproduced with permission from ref. 152. Copyright Elsevier Scientific Publishing Co.)...

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