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VI River Water Used in the Test

VI Ro Values of Some10 Sugars and Sugar Derivatives

VI Rotational Diffusion Constants , and Quotients of the Rotational Diffusion Constants for Compound 31

VI Sampling of Ethylene Oxide in Humid Air, RH 85

VI SAR Variation

VI Sarcoma Genomics

VI Selected Calculated Bond Lengths and 24

VI Selected Calculated Bond Lengths and 24a b

VI Selected Examples of Unusual Transamination Reactions

VI Selected Physical and Thermochemical Data for Pentafluoroethyl.

VI Selected Polymers and Blends Investigated for use as the Skin Layer

VI Separation of Functionally Substituted Hydrocarbons Over H-ZSM-5

VI Short-lived Radicals Found in Aqueous Solution at Room Temperature

VI showed that several ligands exhibited selectivity for Ca2 over Mg2 and Ba2 - this selectivity is small for oxalate and lactate, dramatic for the tetraazamacrocyclic tetracarbox-ylate dota. The familiar aminocarboxylate ligand edta is moderately selective for Ca2 over Mg2 1 replacement of the central - relating to ligand selectivity for the alkaline earth metal cations the maximum value for each ligand is highlighted. The central section of this table illustrates the prime importance of matching ligand cavity size to cation radius for cryptands. In the case of the oxine carboxylate complexes, it is the steric constraint imposed by the two linked five-membered chelate rings that causes the low

VI shows a comparison of the leveling properties of the ortho-cresol novolac film that was baked at 225 C for 15 min with those for a uv-hardened film of a 7

VI shows a comparison of the solution times for the various dynamic simulations using the three models. As shown, the reduction in solution time is

VI shows a comparison of the surface properties of the crown and the corresponding open chain compound. The former has a lower aqueous surface tension and a larger molecular area than the latter, reflecting the lower hydrophilicity and the greater rigidity of cyclic POE.

VI shows a hydrocarbon material balance for operation of a neohexane unit. This operation is typical in that pentane and hexane are isomerized together and the recycle ratio is set by the amount of feedstock available and the capacity of the equipment.

VI shows a progression in the intramolecular hydrophobic interaction between two rings. In diphenyl, additivity holds. In di-phenylethane, which has some conformational freedom, there is a small but quite definite interaction. In the tricyclic Compound 3, the rings are held at a definite angle to one another, with no possibility for rotation. Adding log F values for N-methylaniline and toluene, and making a correction for cyclic methylene groups, we obtain an estimate far greater than the experimental log F value.

VI shows a synopsis of the main industrial ED applications in the food sector.

VI shows an example for detecting and isolating problems due to an air blower speed drop absd. The behavior illustrated by this

VI shows examples of laboratory-measured and the substantially higher calculated in situ alkalinities for 10 samples of groundwater from Field 6. The values shown in Figs. 5 and 6 are laboratory, not in situ pH and alkalinities. Higher in situ pH and alkalinity would lead to faster rates of aldicarb residue breakdown. Projections of aldicarb residue degradation by alkaline hydrolysis should be based on in situ pH, alkalinity and temperature. These, like the residue concentrations, vary widely, spatially and temporally.

VI shows Mg excess levels in daily fecal excretions and in composites of 5 and 9-day pools. The subject illustrated in Table VI showed an unusually rapid return of the isotope dose. In this instance a fecal collection period of 5-6 days should have been adequate for recovery of at least 95 of the Ingested tracer.

VI shows results 19 of liquid product analyses from methylcyclopentane converted under conditions of Ph2 0.8 atm. Pmcp 0.2 atm., with X 0.3 wt. Pt on Si02 and Y 420 m. g. silica-alumina, as catalyst components in 0.8-1.4 mm. particle size, and with

VI shows results obtained with a mixture of dimethyl- and ethylcyclohexanes reformed with catalysts of different acidity. The two functions of a reforming catalyst—the acidity and the hydrogenation-dehydrogenation function of the platinum—are balanced carefully for



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