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INDEX olefinic compounds

A titration procedure, ASTM Test Method D1159, Bromine Number of Petroleum Distillates and Commercial Aliphatic Olefins by Electrometric Titration, provides an approximation of olefin content within a sample, while ASTM Test Method D2710, Bromine Index of Petroleum Hydrocarbons by Electrometric Titration, can be valuable for determining trace olefin levels. These methods do not directly measure total olefins, and the results are affected by the type of olefinic compound present. [Pg.21]

In order to locate items of interest in the book, the subject index lists, in addition to chemical operations, types of compounds rather than specific compounds (with a few exceptions). If, for example, readers do not find what they are looking for under the entry fluoroolefins , they may try olefins , double bonds, additions of , etc. [Pg.1305]

The entries in Tables XIV-XXII have been arranged in order of formula, first the carbonyl compound then the olefin, as they would be found in Chemical Abstracts Formula Index. [Pg.349]

The main index headings for search other than the names of specific compounds are Paraffins nitration of Paraffins, nitro Paraffins, from nitration of— Paraffins, dinitro Hydrocaibons, nitration of Nitration of hydrocarbons Nitration of paraffins Petroleum, nitrogen compounds from Olefins, nitro derivatives and Acetylenes, nitro derivatives. These items are not mutually inclusive, e.g., references under Paraffins, nitration of are not necessarily to be found under Nitration of paraffins. In Chemical Abstracts collective index for 1937 to 1946, there are 19 entries under the first heading and 12 entries under the second only 10 are common to both lists. [Pg.396]

An indication of naphtha composition may also be obtained from the determination of aniline point (ASTM D-1012, IP 2), freezing point (ASTM D-852, ASTM D-1015, ASTM D-1493) (Fig. 4.2), cloud point (ASTM D-2500) (Fig. 4.3), and solidification point (ASTM D-1493). And, although refinery treatment should ensure no alkalinity and acidity (ASTM D-847, ASTM D-1093, ASTM D-1613, ASTM D-2896, IP 1) and no olefins present, the relevant tests using bromine number (ASTM D-875, ASTM D-1159, IP 130), bromine index (ASTM D-2710), and flame ionization absorption (ASTM D-1319, IP 156) are necessary to ensure low levels (at the maximum) of hydrogen sulfide (ASTM D-853) as well as the sulfur compounds in general (ASTM D-130, ASTM D-849, ASTM D-1266, ASTM D-2324, ASTM D-3120, ASTM D-4045, ASTM D-6212, IP 107, IP 154) and especially corrosive sulfur compounds such as are determined by the Doctor test method (ASTM D-4952, IP 30). [Pg.91]

Oil industry has a long history of application of NMR spectroscopy for characterization of crude oils, products and oil fractions. The methodology has been mainly ID proton- or carbon-detected experiments. Quantitative NMR and NMR experiments have been used in estimation of aromatic, olefin, naphtene and paraffin proportions in the samples. ° A more detailed characterization has been obtained using various ID carbon-detected experiments, like GASPE, CSE, QUAT and DEPT to obtain quantitative CH sub-spectra. " The goal of characterization of the oil fractions and quantification of certain structural features has been to find correlation between these features and the product properties (e.g. viscosity index, pour point). Due to environmental concerns oil companies are nowadays more interested in development of lubricant base oils that have low aromatic and olefin contents. Hydrogenation of unsaturated components also improves the stability of the base oils, which is an important property for the end-product. Quantitative analysis of a saturated oil fraction with NMR is a major challenge. When the oil fraction contains only aliphatic compounds, the spectrum width that contains the resonances narrows to ca. 1 ppm in the NMR spectrum and ca. 50 ppm in NMR spectrum. This causes excessive... [Pg.25]

A new structure-activity relationship, Xjj =yS+l, where y is a negative constant, S is the total steric effect, and 4 is the total inductive effect, correlated strongly with available measurements of ozonolysis. New rate coefficients were measured for ozonolysis of a number of unsaturated heteroatomic compounds and it has been emphasized that the inductive effect rather than the steric effect is important in predicting their reactivity %, the inductive effect index, was compared with the Taft a constant and rates of reaction of hydroxyl radical with a given species it correlated strongly in both cases (which should be unaffected by steric factors) suggesting a universal response by olefinic species towards electrophilic addition. ... [Pg.134]

Paraffins can be separated from mixtures with other solvents almost quantitatively by using a mixture of 170 parts of 85% phosphoric acid (q = 1.7) and 100 parts of concentrated sulfuric acid (q = 1.84). Oxygen-containing compounds dissolve, and hydrocarbons remain undissolved in this mixture. Only some reactive olefins can partly form monoesters of sulfuric acid. The process is carried out with cooling, and the reduction in the volume of the upper layer, as well as the change of its refractive index, are followed. The procedure can be considered as completed when both the volume and the refractive index become constant. If a mixture of sulfuric acid and phosphorus pentoxide is used, olefins and aromatic compounds also react, so that enly paraffins remain undissolved (1). [Pg.117]


See other pages where INDEX olefinic compounds is mentioned: [Pg.118]    [Pg.89]    [Pg.412]    [Pg.169]    [Pg.268]    [Pg.421]    [Pg.262]    [Pg.333]    [Pg.766]    [Pg.1254]    [Pg.228]    [Pg.590]    [Pg.80]    [Pg.24]    [Pg.235]    [Pg.108]    [Pg.112]    [Pg.178]    [Pg.365]    [Pg.413]    [Pg.268]    [Pg.339]    [Pg.1029]    [Pg.2]    [Pg.91]    [Pg.211]    [Pg.567]    [Pg.1897]    [Pg.1898]    [Pg.175]    [Pg.110]    [Pg.60]    [Pg.333]    [Pg.6]    [Pg.280]    [Pg.156]   
See also in sourсe #XX -- [ Pg.296 , Pg.297 , Pg.298 , Pg.299 ]




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