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General table

These specifications and characteristics are defined with references to standard test methods which the different parties to a contract should conduct for quality control. The tables that follow show specifically the standards that are applicable in France, but a more general table in Appendix 2 shows the main test methods commonly referenced in specifications. [Pg.297]

The low thermal conductivity of PCM is an intrinsic property of nonmetallic liquids in general (Table 18-21). It poses a problem, because PCM store a large amount of heat in a small volume and this heat has to be transferred through the surface of this volume to the outside to be used in a system. [Pg.268]

Properties of the paraffin hydrocarbons ( C H 2,1-2) exhibit some approximate relationships that are sometimes used to describe common fuels generally. Table 4.6 show some data [5]. [Pg.102]

In general, tables summarize, group, and highlight numerical data so that the data can be viewed collectively. [Pg.533]

This system classifies the local turbulence conditions into classes A through F, where class A denotes the most anticipated turbulence, or the most unstable conditions, and class F denotes the most stable conditions. The class is determined for a particular location at a particular time, based on wind speed, cloud cover, and sun angle. At least two websites currently present tables for determining the local stability class. A government site14 presents a step-by-step procedure to precisely determine the class. A commercial site15 presents a more generalized table. [Pg.100]

ISO 4200, Plain end steel tubes, welded and seamless—General tables of dimensions and masses per unit length. ISO 5753, Rolling bearings— Radial internal clearance. [Pg.12]

Biocatalysis in Biphasic Systems General Table 8.1 Some recent examples of biphasic systems in biocatalysis. [Pg.208]

The five charts mentioned could be incorporated into the general Table I with the notations <25 or >25 (or 20) under CST but this would expand that table considerably without giving much information. Instead they are presented in rearranged and condensed form. However, the large table serves as an index to these tables. The tables are arranged chronologically. [Pg.8]

Thermal /fevrirume—K-valui—Thermal data in general Tables, as Table 2. are for dry materials, and for one or two mean temperatures, but most materials are not linear with mean temperature, hence, for specific designs, the whole ranee of resistance should be obtained. [Pg.855]

General Conference on Weights and Measures http //www.sizes.com/indexes.htm General Tables of Units of Measurement http //ts.nist,gov/ts/htdocs/230/235/appxc/... [Pg.1645]

This reaction seems to be general (Table II), and the diols formed may be easily dehydrated to give the corresponding long-chain conjugated polyene. Substituted butadienes react similarly. [Pg.38]

Generally, tables having up to 6 columns will fit in a single journal column tables having up to 13 columns will fit in the double-column spread. Tables that exceed the double-column spread will be rotated 90° and set lengthwise on the page. [Pg.370]

Other general tables that are less encyclopedic but often easier to use are listed below. [Pg.703]

The literature is replete with pharmacological, histological and biochemical effects produced by known carcinogens. Many of the effects appear within a few hours (or days) and disappear within several weeks of exposure. Many investigators feel that such indicators can be expected generally. Table XVII addresses precancerous signs. [Pg.232]

General. Table II presents the results (on a total-liquid basis) obtained from separation of the oils and asphaltenes into acids, bases, and neutrals and... [Pg.60]

Work with other dienes, such as isoprene and pentadiene-1,3, indicates that coordination control of stereoselectivity by cyanide ion is rather general (Tables IV and V). On the other hand, the reduction of the homoconjugated norbornadiene results in the same distribution of products (7% norbornene, 93% nortricyclene) at both high and low cyanide concentrations. Presumably, a 7r-homoallylic complex (21) is not involved in this case. [Pg.223]

SnI, Sn2, El, E2 How can you keep it all straight How can you predict what will happen in any given case Will substitution or elimination occur Will the reaction be bimolecular or unimolecular There are no rigid answers to these questions, but it s possible to recognize some trends and make some generalizations (Table 11.4). [Pg.423]

All the c.p. layer sequences are possible for AX3 layers, and it is found that those most frequently adopted are the simplest ones having only one or two kinds of non-equivalent sphere, namely, those sequences which repeat after every 2, 3,4, 6, 9, or 12 layers. Examples of structures based on c.p. AX3 layers are included in the more general Table 4.4 (p. 134). Many compounds crystallize with more than one type of closest packing, for example, BaMn03 with the 2, 4, and 9 layer... [Pg.151]

The possible structures for hexagonal and cubic close packing are listed, with examples, in Table 10.15, which corresponds to the portion of the more general Table 4.6 (p. 142) for one-half octahedral holes occupied . In the ideal c.p. structures the coordination group around a metal atom is an octahedral group (of 4 OH + 2 X or 5 OH + X) in which the M—0 and M—X bonds have their normal lengths. As in the case of other cupric compounds there are distortions of the... [Pg.411]

Torsion about one of the formal double bonds is invariably the most efficient excited singlet state decay process of acyclic polyenes, and also often occurs efficiently in cyclic systems of moderate-to-large ring size- . E.Z-isomerization in the excited singlet state manifold takes place about only one of the double bonds per photon, as was initially demonstrated for 2,4-hexadiene (5) by Saltiel and coworkers and has since been shown to be quite general. Table 1 contains a summary of quantum yields for the direct E,Z-photoisomerization, in solution, of acyclic and cyclic polyenes 1, 42, 43, 5-18 bearing various substituents. For the most part, quantum yields for direct E,Z-photoisomerization of aliphatic dienes are not highly dependent on the structure of the system (i.e. acyclic, cyclic or exocyclic). [Pg.203]


See other pages where General table is mentioned: [Pg.405]    [Pg.126]    [Pg.607]    [Pg.203]    [Pg.250]    [Pg.74]    [Pg.458]    [Pg.631]    [Pg.217]    [Pg.150]    [Pg.277]    [Pg.297]    [Pg.56]    [Pg.139]    [Pg.83]    [Pg.371]    [Pg.433]    [Pg.385]    [Pg.703]    [Pg.421]    [Pg.5634]    [Pg.867]    [Pg.42]    [Pg.132]    [Pg.296]    [Pg.187]    [Pg.277]    [Pg.203]    [Pg.160]   
See also in sourсe #XX -- [ Pg.13 ]

See also in sourсe #XX -- [ Pg.13 ]




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