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IV gives the melting points of several dichlorocarbodiimides obtained from substituted ureas and phosgene .

IV gives the names and some properties of the four alkaloids isolated from this Australian plant.

IV gives the properties of a representative series of 3-nitroso-2-oxazolidones.

IV gives the properties of the SRC-II fuel oil compared to a low-sulfur residual oil utilized in a recent combustion test. The SRC-II fuel oil is a distillate product with a nominal boiling range of 350-900 F, a viscosity of 40 Saybolt seconds at 100 F and a pour point below -20 F. Thus, it is readily pumpable at all temperatures normally encountered in transportation of the fuel oil. The fuel oil has a very low content of ash and sediment as well as a low Conradson carbon residue. These characteristics are favorable from the standpoint of particulate emissions during combustion. Tests of compatibility with typical petroleum fuel oils and on stability of the coal distillates over time have not revealed any unusual characteristics that would preclude utilization of these coal-derived fuels in conventional boiler applications.

IV gives the recipe used to prepare these copolymers.

IV gives the relative catalytic reactivities of the various ions calculated on the basis that the undissociated ion given is the catalytic species.

IV gives the relative product distribution from the vacuum ultraviolet photolysis of ethyl chloride at 40 mm. pressure using the 1236-A. krypton resonance line. Owing to the low intensity of emission from the resonance lamp, higher pressures were not used in the photolysis experiments in order to prevent the major portion of the reaction from occurring in the region of the window where surface interactions are likely. Therefore, to provide a basis for more direct comparison between the photolytic and radiolytic yields, the radiolysis of ethyl chloride was also examined at 40 mm. pressure. The relative yields from several experiments of the latter study are given in Table IV. The lowest conversion yields from the radiolysis at the lower pressure show a relative distribution which is in close agreement with the relative product distribution detected from the radiolysis at 357 mm. Therefore, there is no substantial pressure effect on the decomposition product yields in ethyl chloride over the range 40-357 mm.

IV gives the results for several analysis procedures of the hyperfiltration concentration and permeate at three different recovery levels. The rejections based on the analysis types are provided in Figure 11. Concentration has little effect on the rejections of the constituents tested.

IV gives the retention and product flux for membranes cross-linked by dicarbonyl compounds in presence of various aqueous solutions of phenol, sodium sulfide, pyridine and eumnonia. The strong concentration dependence of the retention in the presence of phenol and the dependence of the flux on the solute is interesting. Membranes with 95 retention for phenol at fluxes of about O.lOO m can be easily obtained.

IV gives the Rf values determined under these conditions. Figure 3 shows the chromatograms of the reaction products of the re-esterification of a number of plasticizers. It is obvious that the method is suitable for identifying the alcohol components of all frequently used ester types. Difficulties have been met with phenolic components although they are present primarily in phosphoric acid esters. To identify these, evaporate to dryness a few drops of the reaction mixture of an alkaline saponification and mix this with a bit of the precipitated alkali salt. Add this residue to 10 to 20 drops of chloroform and gradually evaporate it repeat

IV gives the species flows for a five-species alcohol mixture. Design a system of distillation columns to separate them.

IV gives the spin densities calculated on the water oxygen for P450 j2 and for comparison, in MMB. Experimental values of Pgff and our calculated results indicate MMB is in a high-spin

IV gives the values of various control rod configurations for both the hot and the cold core.

IV gives UV spectrophotometric data, the first column giving wavelength of the principal peak, the second the name of the compound.

IV gives values of J when the false positive rate is 5 percent and the false negative rate is either 5 percent or 1 percent. J depends on V and, since K 1, on the sura a a . A

IV Globalization

IV Glutamic-Oxalacetic Transaminase Activity of Animal and Plant Tissues and Microorganisms

IV Glycosidation with Perbenzoylated Phenyl Selenogiycoside 177 Entry Donor Acceptor Disaccharide Yield

IV Goodrich Disk Fatigue Testing Strength Retention,

IV Grazing Capacity Loss Due to Shrub Invasion on Four Properties Located West of Wanaaring

IV Group Separation of Amino Acids and Peptides according to Jutisz and Lederer 1947

IV Groups of Natural Galactocerebrosides

IV Growth inhibition of the plant pathogens by the microbial cultures of antifungal agents

IV Guanidinated Peptide 1-16

IV H Chemical Shifts of Structural- reporter Croups of Constituent Monosaccharides for Asialo-agalacto Di-, and Asialo Di-, Tri-, Tri -, and Tetra-antennary Oligosaccharides



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