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Secondary release containment

Secondary release problems arise from various adhesive forces between the briquette and cup. Obviously, pockets cannot contain any reentrant surface because, as the pockets part, the briquette would get caught and tend to split in half. Similar forces can be caused by friction between the briquette and cup and on surfaces nearly parallel to the roller radius (see Figure 252a). [Pg.297]

The reaction involves initial formation of the zirconium-imido species, followed by [2-1-2] cycloaddition with the C—C unsaturation (Scheme 13). This is consistent with the observation that bis(amidate) complexes do not mediate hydroamination with secondary amine containing substrates. The cyclic transition state of the intramolecular reaction determines the regioselectivity of the reaction followed by successive protonation of the intermediate metallacycle and release of product to regenerate the catalyticaUy active imido species. [Pg.389]

This potential design improvement consists of providing the middle and lower atmulus of the secondary concrete containment with a passive annulus filter system, for filtration of elevated releases. The passive filter system would be operated by drawing a partial vacuum on the middle annulus through charcoal and high efficiency particulate in air filters. The partial vacuum is... [Pg.392]

A volatile oil contains a relatively large fraction of lighter and intermediate oomponents which vaporise easily. With a small drop in pressure below the bubble point, the relative amount of liquid to gas in the two-phase mixture drops rapidly, as shown in the phase diagram by the wide spacing of the iso-vol lines. At reservoir pressures below the bubble point, gas is released In the reservoir, and Is known as solution gas, since above the bubble point this gas was contained in solution. Some of this liberated gas will flow towards the producing wells, while some will remain in the reservoir and migrate towards the crest of the structure to form a secondary gas cap. [Pg.104]

Method 2. Place a 3 0 g. sample of the mixture of amines in a flask, add 6g. (4-5 ml.) of benzenesulphonyl chloride (or 6 g. of p-toluenesulphonyl chloride) and 100 ml. of a 5 per cent, solution of sodium hydroxide. Stopper the flask and shake vigorously until the odour of the acid chloride has disappeared open the flask occasionally to release the pressure developed by the heat of the reaction. AUow the mixture to cool, and dissolve any insoluble material in 60-75 ml. of ether. If a solid insoluble in both the aqueous and ether layer appears at this point (it is probably the sparingly soluble salt of a primary amine, e.g., a long chain compound of the type CjH5(CH2) NHj), add 25 ml. of water and shake if it does not dissolve, filter it off. Separate the ether and aqueous layers. The ether layer will contain the unchanged tertiary amine and the sulphonamide of the secondary amine. Acidify the alkaline aqueous layer with dilute hydrochloric acid, filter off the sulphonamide of the primary amine, and recrystaUise it from dilute alcohol. Extract the ether layer with sufficient 5 per cent, hydrochloric acid to remove all the tertiary amine present. Evaporate the ether to obtain the sulphonamide of the secondary amine recrystaUise it from alcohol or dilute alcohol. FinaUy, render the hydrochloric acid extract alkaline by the addition of dilute sodium hydroxide solution, and isolate the tertiary amine. [Pg.651]

The lead-bearing components ate released from the case and other nordead-containing parts, followed by the smelting of the battery plates, and refinement to pure lead or specification alloys. The trend toward battery grid alloys having Httle or no antimony, increases the abiHty of a recovery process to produce soft lead (refined). As requited in the production of primary lead, each step in the secondary operations must meet the environmental standards for lead concentration in ait (see Air pollution Lead compounds, industrial toxicology). [Pg.48]

Personnel are protected in working with tritium primarily by containment of all active material. Containment devices such as process lines and storage media are normally placed in well-ventilated secondary enclosures (hoods or process rooms). The ventilating air is monitored and released through tall stacks environmental tritium is limited to safe levels by atmospheric dilution of the stack effluent. Tritium can be efficiently removed from air streams by catalytic oxidation followed by water adsorption on a microporous soHd absorbent (80) (see Absorption). [Pg.16]

As an example, the low-density lipoprotein (LDL) molecule and its receptor (Chapter 25) are internalized by means of coated pits containing the LDL receptor. These endocytotic vesicles containing LDL and its receptor fuse to lysosomes in the cell. The receptor is released and recycled back to the cell surface membrane, but the apoprotein of LDL is degraded and the choles-teryl esters metabolized. Synthesis of the LDL receptor is regulated by secondary or tertiary consequences of pinocytosis, eg, by metabolic products—such as choles-... [Pg.430]

Transfer facilities, processors and rerefiners, and burners must also have secondary containment systems to prevent oil from reaching the environment in the event of a spill or leak. Secondary containment consists of an oil-impervious dike, berm, or retaining wall to contain releases, as well as an oil-impervious floor to prevent migration. [Pg.444]

Residual. This fraction mainly contains primary and secondary minerals, which hold elements within their crystal structure. This fraction also contains trace elements remained from the extraction of all previous fractions (e.g., humin bound). These metals/trace elements are not expected to be released into soil solutions over a reasonable time span under conditions normally encountered in nature. [Pg.108]

Experiment 1. Visual observation of secretory cells in luminescence microscope Various types of secretory cells in allelopathically active plants contain fluorescing secondary products (Fig. 1). Secretions from the above ground parts of plant (in leaves, flowers, stems) were concentrated in secretory hairs and glands. Whereas secretions of roots are in secretory reservoirs and idioblasts (ordinary cells which accumulate secretory products) or may be released by the secretory surface of the root tip (Fig. 1.). The fluorescence appears to change, when allelopathically active cell of other plant species (cell-donor) interacts with acceptor cell (Roshchina and Melnikova, 1999). [Pg.125]

Figure 1.116 Released glycans can be labeled with small fluorescent compounds containing amines for subsequent detection upon chromatographic separation. In the presence of sodium cyanoborohydride these compounds react at the reducing end of glycans to form secondary amine derivatives with characteristic spectral properties. Figure 1.116 Released glycans can be labeled with small fluorescent compounds containing amines for subsequent detection upon chromatographic separation. In the presence of sodium cyanoborohydride these compounds react at the reducing end of glycans to form secondary amine derivatives with characteristic spectral properties.

See other pages where Secondary release containment is mentioned: [Pg.33]    [Pg.142]    [Pg.33]    [Pg.142]    [Pg.396]    [Pg.103]    [Pg.531]    [Pg.33]    [Pg.218]    [Pg.218]    [Pg.142]    [Pg.70]    [Pg.105]    [Pg.107]    [Pg.320]    [Pg.322]    [Pg.342]    [Pg.336]    [Pg.2310]    [Pg.201]    [Pg.42]    [Pg.437]    [Pg.770]    [Pg.328]    [Pg.344]    [Pg.454]    [Pg.552]    [Pg.99]    [Pg.535]    [Pg.96]    [Pg.439]    [Pg.258]    [Pg.266]    [Pg.251]    [Pg.11]    [Pg.197]   
See also in sourсe #XX -- [ Pg.32 , Pg.91 ]

See also in sourсe #XX -- [ Pg.32 , Pg.91 ]




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