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V shows the comparative elemental analyses of the surficial sediments obtained from the seven stations by box coring and the CS system. Three elements were selected for comparison because of their presence in high levels in the marine sediments and the good sensitivity for detection by the Perkin-Elmer AA, the Philips XRF, and the ship-

V shows the comparison of two experiments run at the same experimental conditions but using the two different types of nitrogen. A much better agreement was found between the Ca2 conversion estimated by integration of the SO2 curve was the same in both experiments indicating that the rate of SO2 removal is not affected by the nitrogen purity even when some oxidation of the

V shows the complications and outcome of the infants receiving total intravenous alimentation.

V shows the composition of the liquid meals for this study. As in the previous study, two levels each of cottage cheese and beef were fed to the subjects. In addition, 45 g of protein from soy isolate was also fed. The phytic acid content of this meal was 126 mg. A basal diet containing all nutrients except protein was also included in this study. It was necessary to reduce the fat content of the basal diet for palatability the total energy for this meal only was 250 kcal. In this study, the calcium and phosphorus levels of each meal were equalized across all levels and sources of protein. Levels of other meal components were maintained as constant as possible and are shown at the bottom of Table V.

V shows the computations by Hwu for FT — H in a methane-propane mixture in comparison with the predictions of Mollerup using the VDW one-fluid theory with shape factors. The improvement of the HSE method is very slight. The theoretical advantages of the HSE method for enthalpy calculations may be offset here by using a generally poorer reference equation of state than that used by Mollerup.

V shows the concentrations of individual low-molecular-weight hydrocarbons in the water samples collected. The highest total concentration was 60 u,g L . Total hydrocarbon concentrations in the other four samples ranged from 2 to 16 ppb. The difference is probably due to higher winds at the time of the first Murban spill.

V shows the concentrations of polymer , the GPC that they were directly injected into, and the Column Code involved Ref.

V shows the DDT spray residues at harvest on Delicious and Winesap apples in the Yakima Valley. Most of the Delicious plots received two sprays containing DDT, the last one 97 days before harvest. The Winesap plots received four sprays containing DDT, the last spray 74 days before harvest. The harvest residues in the Winesap plots were significantly higher than those in the Delicious plots, but were less than one half the proposed tolerance of 7 p.p.m. of DDT.

V shows the differences in the freeze-thaw durability of concrete-polymer specimens receiving radiation and thermal treatment. The data indicate that the thermally treated specimens have either the same or slightly better durability than the radiation treated material. The higher durability, however, may be related to the higher polymer loading present in the thermal samples for this series of tests.

V shows the distribution of the alkaloids isolated from plants of the genus Stephania by species. Analysis of the data contained in the table led to some observations about the genus

V shows the effect of Ti, Zr, and Sn addition when excess antimony was present. Although each Increased catalyst activity, the effect was much smaller than for the USb. M Oy compositions. Titanium addition about doubled the relative activity compared to the standard uranium-antimony oxide catalyst, while Zr and Sn addition had a smaller effect. The poor selectivity of the Distillers-type catalyst. No. 9, is attributed to the presence of USbO.

V shows the effect of wastewater treatment level on the cost-effectiveness of a hypothetical 1-MGD algae pond system in Greensboro. NC, as a base case. Cash flow decreases as the level of treatment increases. For

V shows the efficient organization of this reaction chemistry into five reaction families. Bond fission, for example, is the elementary step that creates two free radicals from a parent molecule. In chain processes this will often be the initiation step. Thermochemical estimates often show that the logarithm of the Arrhenius A factor . This equality is the result of the essentially unactivated reverse reaction step, radical recombination.

V shows the first CDR of seven other VKIII light chains and of LAY and POM while anti-human IgG specificity is directed against protein determinants.

V shows the influence of the reaction temperature especially in connection with the course of isomerization reactions

V shows the main characteristics of each of the reactors built in the countries that participated in TC Regional Project RLA 4 018.

V shows the number of hydrogen bonds per water molecule calculated by integrating the goH up to the first minimum, in the conditions of the four different simulations.

V shows the relative amounts of III, IV, and V found in different solvents under variable experimental conditions.

V shows the relative importance of the model terms, by

V shows the relative rates for addition at 150 and most of the data comes from Tables III and IV. However two radicals are included in this Table for which no accurate temperature variation is available. The general pattern of results confirms the picture built up from the tables of relative Arrhenius Parameters. The relative rates are the results of direct measurement and therefore probably represent a more accurate summary. A very noticeable feature of Table V is the low rates of addition of heptafluoro-iso-propyl radicals to CHF- and CF2- sites. This strongly suggests that classical steric hindrance plays a significant role in free radical addition.

V shows the results for oxygen. The adsorption or permeation process is apparently very strongly affected by the pressure used in pretreating the tube with oxygen. The apparent leak rate is roughly proportional to the square root of the pressure. One explanation of this law may be that the adsorption or surface diffusion of the gas is atomic in nature.

V shows the results obtained for the carbonylation of dimethyl ether and methyl acetate with molybdenum catalysts supported on various carrier materials. In the case of dimethyl ether carbonylation, molybdenum-activated carbon catalyst gave methyl acetate with an yield of 5.2 which was about one-third of the activity of nickel-activated carbon catalyst. Silica gel- or y-alumina-supported catalyst gave little carbonylated product. Similar results were obtained in the carbonylation of methyl acetate. The carbonylation activity occured only when molybdenum was supported on activated carbon, and it was about half the activity of nickel-activated carbon catalyst.

V shows the results of our measurements. The reaction rate time functions of three emulsions with lowest, medium, and highest emulsifier concentration are shown in Figure 12. Periods II and III become indistinguishable at the lowest emulsifier concentrations studied by us

V shows the results of this analysis for the Pn-helix fraction of several proteins denatured by heat, cold, acid, and Gdm HCl urea. There is rather good consistency among the estimated Pn-helix contents for proteins denatured by a given agent, except for acid-denatured proteins, which show more variability. The chemically denatured proteins have 30 5 Pn-helix content near 0 C. At the other extreme, heat-denatured proteins have Pn-helix contents near 0 , with lysozyme having the highest value . Although there are only two examples of cold-denatured proteins in Table V,2 they both have Pn-helix contents of about 20 . Acid-denatured proteins have Pn-helix contents ranging from 0 to 16 .

V shows the results of this experiment. The major products were propene and carbon oxides, with small amounts of cracked products. In the

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