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Water molecular sieve

Remove traces of ethanol and dissolve precipitate in a minimum (10 ml) of distilled water. Molecular sieving on a Sephadex G25 fine column (1300 ml, 0 5 cm). Assay fraction for /3-poly(L-malate) and chloride ions. Use only salt-free fractions. [Pg.95]

Cassidy and Niro [13] have applied high-speed liquid chromatography combined with infrared spectroscopy to the analysis of polyoxyethylene surfactants and their decomposition products in industrial process waters. Molecular sieve chromatography... [Pg.104]

Figure 6.7 Gas purification system for removal of oxygen (BTS catalyst) and water (molecular sieves). Figure 6.7 Gas purification system for removal of oxygen (BTS catalyst) and water (molecular sieves).
Cassidy and Niro [13] have applied high-speed liquid chromatography combined with infrared spectroscopy to the analysis of polyoxyeihylene surfactants and their decomposition products in industrial process waters. Molecular sieve chromatography combined with infrared spectrometry give a selective method for the analysis of trace concentrations of these surfactants. These workers foimd that liquid-solid chromatography and reversed phase chromatography are useful for the characterisation and analysis of free fatty acids. [Pg.107]

This type of analysis requires several chromatographic columns and detectors. Hydrocarbons are measured with the aid of a flame ionization detector FID, while the other gases are analyzed using a katharometer. A large number of combinations of columns is possible considering the commutations between columns and, potentially, backflushing of the carrier gas. As an example, the hydrocarbons can be separated by a column packed with silicone or alumina while O2, N2 and CO will require a molecular sieve column. H2S is a special case because this gas is fixed irreversibly on a number of chromatographic supports. Its separation can be achieved on certain kinds of supports such as Porapak which are styrene-divinylbenzene copolymers. This type of phase is also used to analyze CO2 and water. [Pg.71]

Catalytic system addition of molecular sieves to "soak" up any water with 3A sieves, 5-10 mol % catalyst is used,... [Pg.26]

Fig. 1. Water isotherms for various adsorbents (1). Activation conditions Linde molecular sieves, 350°C and <1.33 Pa activated alurnina, 350°C and... Fig. 1. Water isotherms for various adsorbents (1). Activation conditions Linde molecular sieves, 350°C and <1.33 Pa activated alurnina, 350°C and...
Isotherms for H2O and / -hexane adsorption at room temperature and for O2 adsorption at Hquid oxygen temperature on 13X (NaX) zeoHte and on the crystalline Si02 molecular sieve siHcaHte are are shown in Figure 8 (43). SiHcaHte adsorbs water very weaMy. Further modification of siHcaHte by fluoride incorporation provides an extremely hydrophobic adsorbent, shown in Figure 9 (44). These examples illustrate the broad range of properties of crystalline molecular sieves. [Pg.276]

To prevent such release, off gases are treated in Charcoal Delay Systems, which delay the release of xenon and krypton, and other radioactive gases, such as iodine and methyl iodide, until sufficient time has elapsed for the short-Hved radioactivity to decay. The delay time is increased by increasing the mass of adsorbent and by lowering the temperature and humidity for a boiling water reactor (BWR), a typical system containing 211 of activated carbon operated at 255 K, at 500 K dewpoint, and 101 kPa (15 psia) would provide about 42 days holdup for xenon and 1.8 days holdup for krypton (88). Humidity reduction is typically provided by a combination of a cooler-condenser and a molecular sieve adsorbent bed. [Pg.285]

Sohd sorbent materials have the abiUty to adsorb water vapor until an equiUbrium condition is attained. The total weight of water that can be adsorbed in a particular material is a function of the temperature of the material and of the relative humidity of the air (see Adsorption). To regenerate the sorbent, its temperature must be raised or the relative humidity lowered. The sohd sorbents most commonly used are siUca (qv), alumina (see Aluminum compounds), and molecular sieves (qv). [Pg.362]

By-product water formed in the methanation reactions is condensed by either refrigeration or compression and cooling. The remaining product gas, principally methane, is compressed to desired pipeline pressures of 3.4—6.9 MPa (500—1000 psi). Einal traces of water are absorbed on siHca gel or molecular sieves, or removed by a drying agent such as sulfuric acid, H2SO4. Other desiccants maybe used, such as activated alumina, diethylene glycol, or concentrated solutions of calcium chloride (see Desiccants). [Pg.75]

Dry inlet gas that has been dehydrated by molecular sieves (qv) or alumina beds to less than 0.1 ppm water is spHt into two streams by a three-way control valve. Approximately 60% of the inlet gas is cooled by heat exchange with the low pressure residue gas from the demethanizer and by external refrigeration. The remainder of the inlet gas is cooled by heat exchange with the demethanized bottoms product, the reboiler, and the side heater. A significant amount of low level refrigera tion from the demethanizer Hquids and the cold residue gas stream is recovered in the inlet gas stream. [Pg.182]

Solid-Bed Dehydration. Sihca gel, bauxite, activated alurnina, or molecular sieves can be used for removing dissolved water to meet propane specifications. The soHd-bed dehydrators are used in a cycHc adsorption process. After an adsorption cycle has completed, the bed is heated with a purge gas or a vaporized Hquid-product stream for regeneration. If the latter is used, the Hquid product is condensed, separated from the free water, and returned to the process. After the beds are regenerated, they are cooled and returned to the adsorption cycle. [Pg.185]

Molecular Sieve Treatment. Molecular sieve treaters can be designed to remove H2S, organic sulfur compounds (including carbonyl sulfide), and water in one step. SoHd-bed units are utilized and regeneration occurs in the same manner as simple, soHd-bed dehydrators. [Pg.185]

Some commercially available molecular-sieve products and related materials are shown in Table 6, classified according to the basic 2eohte stmcture types. In most cases, the water content of the commercial product is below 1.5—2.5 wt % certain products, however, are sold as fully hydrated crystalline powders. [Pg.455]

Molecular sieves have had increasing use in the dehydration of cracked gases in ethylene plants before low temperature fractionation for olefin production. The Type 3A molecular sieve is size-selective for water molecules and does not co-adsorb the olefin molecules. [Pg.456]

Another nonregenerative drying appHcation for molecular sieves is their use as an adsorbent for water and solvent in dual-pane insulated glass windows. The molecular sieve is loaded into the spacer frame used to separate the panes. Once the window has been sealed, low hydrocarbon and water dew points are maintained within the enclosed space for the lifetime of the unit. Consequently, no condensation or fogging occurs within this space to cloud the window. [Pg.456]

Gas and Hquid dehydrators employing molecular sieves provide product gas streams of <0.1 ppmv water and product Hquid streams routinely to <10 ppmv water. AppHcable pressures range from less than one to several hundred times atmospheric pressure. Temperatures range from subzero to several hundred °C. Processing units range in capacity from as Httle as 10 m /h to as much as 10 mr /d in multiple-train units. [Pg.456]


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See also in sourсe #XX -- [ Pg.22 , Pg.192 ]




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