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Indicated hydrogen method

This method of locating bridging hydrogen atoms is adapted from the indicated hydrogen method in organic nomenclature (see Section P-14.6 of Ref. 1). The indicated hydrogen method would yield the name (2,3-p7U,(2,5-p//),(3,4-p77),(4,5-p/T)-M °-pentaborane(9). [Pg.94]

The effects of reactor type, process variables and feedstock type, catalysts, and feedstock composition (Chapters 5 and 6) on the desulfurization process provide a significant cluster of topics through which to convey the many complexities of the process. In the concluding chapters, examples and brief descriptions of commercial processes are presented (Chapter 7) and, of necessity, some indications of methods of hydrogen production (Chapter 8) are also included. [Pg.9]

Due to the low thickness of this sample, approximately 25pm, no determination of a lag time was possible. Testing using mass spectrometer generally indicated hydrogen at near saturation levels within the first sampling frequency, which is limited to about 15 seconds for the instrumentation used. The data were analyzed using the standard data reduction method and the permeability of this alloy is indicated in Table 3. [Pg.295]

American practice in forming a names is based on the skeletal system, sometimes with the use of indicated hydrogen. This practice differs from the European method. Thus American practice gives lJF/-2-oxapyrene whereas European chemists name the same compound 2-oxa-l,2-dihydropyrene. The "a names must... [Pg.62]

The reduction of M0O3, by a variety of methods, gives compounds Mo03 c(OH) c (0 5indicate hydrogen bonds. l In M0O3 the metal atoms are displaced... [Pg.529]

The infiuence of water on the reaction between ammonia and hydrogen chloride to form ammonium chloride may be taken up in the same way. Although very little is known of the way the water actually catalyzes the formation of ammonium chloride, the reaction considered in Chapter IV in the formation of tetraethylammonium iodide from triethyl amine and ethyl iodide in the presence of different solvents indicated the method of action of the catalyst. It was found that unsaturation of the solvent paralleled to a certain extent the increase in the velocity of the reaction. Ability to form addition compounds, intermediate or otherwise, seemed to be the controlling factor. Unfortunately, the composition of the intermediate addition compound is not so definite in the present case. In order... [Pg.79]

Recent studies(22,23) have indicated several methods for disrupting the hydrogen bonding that promotes helix formation in fermentation carbohydrate polymers ( e.g., alkalinity in SGPS, urea in XCPS solutions). The influence of urea is less marked in SGPS solutions, probably due to the absence of an acid-base reaction. The addition of... [Pg.256]

We have used the tandem ADMET/hydrogenation method to produce a series of model EVA copolymers with pendant acetate functionality on every 19, 2V 23, and 2T carbon atom along the polyethylene backbone Figure 2, polymer 3, n = 18, 20, 22, and 26) [23]. Molecular weight analysis by GPC indicates that all of these polymers are in the range of 30,000 to 70,000 g/mol and have typical ADMET molecular weight distributions (PDI 2). Due to its low (23 °C), the copolymer with n = 18 lacks form stability at room temperature. However, the copolymers with n = 20, 22, and 26 all yield tough films and fibers from solution or the melt, and transparent or- translucent materials can be obtained from the melt. [Pg.312]

Figure 9. Variation in (a) concentration gradient and (b) concentration at jc = L with time for a membrane used in the potentiometric pulse method. Shaded area indicates hydrogen peak generated by cathodic pulse. (After Ref. 11. Reprinted with permission from J. Less Common Metals, Elsevier Sequoia S.A.)... Figure 9. Variation in (a) concentration gradient and (b) concentration at jc = L with time for a membrane used in the potentiometric pulse method. Shaded area indicates hydrogen peak generated by cathodic pulse. (After Ref. 11. Reprinted with permission from J. Less Common Metals, Elsevier Sequoia S.A.)...
Here, and Lj are local indices having the form shown in Eq. (5), where lo is a constant characterizing the ith atom (in some cases the atom valence can be used to this end), Nh is the number of attached hydrogen atoms and is the charge density calculated by some fast method such as the Marsili-Gasteiger charge calculation method [7]. [Pg.295]

A very important difference between H2 and molecular orbital calculations is electron correlation. Election correlation is the term used to describe interactions between elections in the same molecule. In the hydrogen molecule ion, there is only one election, so there can be no election correlation. The designators given to the calculations in Table 10-1 indicate first an electron correlation method and second a basis set, for example, MP2/6-31 G(d,p) designates a Moeller-Plesset electron coiTclation extension beyond the Hartiee-Fock limit canied out with a 6-31G(d,p) basis set. [Pg.312]

Analytical Methods. The official NIOSH recommended method for determining sulfur dioxide in air consists of drawing a known prefiltered volume of air through a bubbler containing hydrogen peroxide, thus oxidising the sulfur dioxide to sulfuric acid. Isopropyl alcohol is then added to the contents in the bubbler and the pH of the sample is adjusted with dilute perchloric acid. The resultant solution is then titrated for sulfate with 0.005 M. barium perchlorate, and Thorin is used as the indicator. [Pg.147]

Analytical Methods. A classical and stiU widely employed analytical method is iodimetric titration. This is suitable for determination of sodium sulfite, for example, in boiler water. Standard potassium iodate—potassium iodide solution is commonly used as the titrant with a starch or starch-substitute indicator. Sodium bisulfite occurring as an impurity in sodium sulfite can be determined by addition of hydrogen peroxide to oxidize the bisulfite to bisulfate, followed by titration with standard sodium hydroxide (279). [Pg.149]

Concentration by gas chromatography has also been demonstrated. Elution chromatography has been used on an activated alumina column to resolve the molecular species H2, HT, and T2, thereby indicating a technique for separation or concentration of tritium (54). This method was extended (55) to include deuterium components. The technique was first demonstrated in 1964 using macro quantities of all six hydrogen molecular species (56). [Pg.15]


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