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O-Water

H2150 is commonly used for myocardial and cerebral perfusion studies. [Pg.136]

Nitrogen-13-labeled ammonia (ty2 = 10 min) is produced by reduction of 13N-labeled nitrates and nitrites that are produced by proton irradiation of water in a cyclotron. The reduction is carried out with titanium chloride in alkaline medium. 13N-NH3 is then distilled and finally trapped in acidic saline solution. Wester et al (1991) has used a pressurized target of aqueous ethanol, in which ethanol acts as a hydroxyl free radical scavenger to improve the [Pg.136]


The theory has certain practical limitations. It is useful for o/w (od-in-water) emulsions but for w/o (water-in-oil) systems DLVO theory must be appHed with extreme caution (16). The essential use of the DLVO theory for emulsion technology Hes in its abdity to relate the stabdity of an o/w emulsion to the salt content of the continuous phase. In brief, the theory says that electric double-layer repulsion will stabdize an emulsion, when the electrolyte concentration in the continuous phase is less than a certain value. [Pg.199]

Gmelin Handbook of Inorganic Chemistry, 8th edn. (in English), O Water Desalting, 1974, 339 pp. [Pg.622]

It has been established that both the 17 hydroxy androgens rind estrogens, when administered orally, are quickly converted (o water-soluble inactive metabolites by intestinal bacteria, usually by reactions at the 17 position. It is this inactivation process that is largely responsible for the low-order oral potency observed with these agents. Incorporation of an additional car-l)on atom at the 17 position should serve to make the now tertiary alcohol less susceptible to metabolic attack and thus potentially confer oral activity to these derivatives. [Pg.161]

Development Development well OO Development well OO Exploration well O Auxiliary well O Production well O - oil - gas Injection well O - water - gas - in-situ combustion Appraisal well OO Development well O... [Pg.29]

Figure 3.16 Effect of initiator on caprolactam polymerization at 260°C (o) water 0.01 mol % (x) aminocaprolic acid 0.01 mol %.28... Figure 3.16 Effect of initiator on caprolactam polymerization at 260°C (o) water 0.01 mol % (x) aminocaprolic acid 0.01 mol %.28...
O Water absorbing polymer Figure 8.26 Asymmetric reduction of ketones in CO2 by Geotrichum candidum immobilized whole cell [20], (a) Time course for the reduction of o-fluoroacetophenone (b) substrate specificity (c) apparatus for C. candidum-cata yzed reduction with semiflow process using scC02. [Pg.214]

Fig. 2. Comparison of the effects of various stress treatments upon reproductive effort in Poa annua. The intensity of each stress treatment is characterised by comparing the growth increment of stressed plants to that of control (unstressed) plants over the same experimental period. , control O, water stress (polyethylene glycol) A, mineral nutrient stress (dilute concentrations of Rorison solution) shading by neutral filters (Smit, 1980). Fig. 2. Comparison of the effects of various stress treatments upon reproductive effort in Poa annua. The intensity of each stress treatment is characterised by comparing the growth increment of stressed plants to that of control (unstressed) plants over the same experimental period. , control O, water stress (polyethylene glycol) A, mineral nutrient stress (dilute concentrations of Rorison solution) shading by neutral filters (Smit, 1980).
Ethylene glycol A Ethanol O Water Heavy water... [Pg.146]

O Water covers about 71 percent of the surface of the earth. Most of it is in the oceans and ice at the North and South Poles, but water is also in clouds, rain, rivers, lakes, and in underground aquifers. [Pg.112]

The extractabilities of metal-organic complexes depend on whether inner or outer sphere complexes are formed. Case 1, section 4.2.1, the extraction of ura-nyl nitrate by TBP, is a good example. The free uranyl ion is surrounded by water of hydration, forming U02(H20)f, which from nitric acid solutions can be crystallized out as the salt U02(H20)6 (N03), though it commonly is written U02(N03)2(H20)6. Thus, in solution as well as in the solid salt, the UOf is surrounded by 6 HjO in an inner coordination sphere. In the solid nitrate salt, the distance du.o(nitrate) between the closest oxygen atoms of the nitrate anions, (0)2N0, and the U-atom is longer than the corresponding distance, du-o(water), to the water molecules, OH2, i.e., du.o(nitrate) > 4u.o(water) thus the nitrate anions are in an outer coordination sphere. [Pg.187]

Figure 9. Effect of the duration of heat treatment at I75°C on salt and water permeabilities of PVA at 30°C (A) salt permeability coefficients (O) water permeability coefficients. Open symbols refer to 100% hydrolyzed, 86,000 mol wt PVA solid symbols refer to ]00%> hydrolyzed, 115,000 mol wt PVA. Figure 9. Effect of the duration of heat treatment at I75°C on salt and water permeabilities of PVA at 30°C (A) salt permeability coefficients (O) water permeability coefficients. Open symbols refer to 100% hydrolyzed, 86,000 mol wt PVA solid symbols refer to ]00%> hydrolyzed, 115,000 mol wt PVA.
The distortion in [Lu(DPM)3(NCeH7)] stems from the fact that the Lu—N bond (2.492 A) is 0.25 A longer than the average Lu—O distance of 2.238 A, while the average chelate bite remains at 2.74 A Hke other /S-diketonate complexes. Such distortion is not uncommon. Even when all seven atoms are oxygens, a long M—O distance contributes to the distortion of the coordination polyhedron as in the case of [Dy(DPM)3(OH2)] (57), where the Dy—O (water) is longer by 0.11 A compared to the Dy—O (chelate) bond. [Pg.94]

Further, in practice, a given emulsion needs to be prepared with some specified range of ratio between oil and water. In such cases, it may be more useful to study mixtures of oil (O), water (W), emulsifier (E), as plots of ratios (Figure 9.3). The region of the most suitable emulsion can be determined by studying varying mixtures. [Pg.180]

FIGURE 9.4 Four-component system Oil (O)-Water (W)-Emulsifier (E)-Cosurfactant (S) (ratio of 0 S versus S W). [Pg.182]


See other pages where O-Water is mentioned: [Pg.209]    [Pg.474]    [Pg.270]    [Pg.20]    [Pg.343]    [Pg.628]    [Pg.439]    [Pg.118]    [Pg.119]    [Pg.8]    [Pg.858]    [Pg.269]    [Pg.151]    [Pg.163]    [Pg.27]    [Pg.265]    [Pg.267]    [Pg.67]    [Pg.208]    [Pg.320]    [Pg.463]    [Pg.173]    [Pg.173]    [Pg.330]    [Pg.113]    [Pg.537]    [Pg.54]    [Pg.568]    [Pg.187]    [Pg.135]    [Pg.136]    [Pg.209]    [Pg.98]    [Pg.118]    [Pg.84]   


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O solubility in water

Water O—H bonds

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