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Vinyl Ethers. The principal commercial vinyl ethers are methyl vinyl ether (methoxyethene, C H O) [107-25-5], ethyl vinyl ether (ethoxyethene, C HgO) [104-92-2], and butyl vinyl ether (1-ethenyloxybutane, C H 20) [111-34-2]. (See Table 8 for physical properties.) Others such as the isopropyl, isobutyl, hydroxybutyl, decyl, hexadecyl, and octadecyl ethers, as well as the divinyl ethers of butanediol and of triethylene glycol, have been offered as development chemicals (see Ethers). [Pg.114]

Physical properties other than magnetic ones are summarized in Table 4, including the influences of porosity and of the measuring direction, ie, parallel ( ) or perpendicular (J ) to the preferred axis. Nearly all properties are clearly anisotropic, the ratio between both values being about 2. For... [Pg.193]

Chemical Intermediates and Reagents. Table 1 Hsts some chemical intermediates and synthesis reagents containing bromine. The references cited in the table generally give a method of synthesis and often some physical properties. Other physical properties are also available (194—196). [Pg.295]

Another attribute of CA dynamics is the average size of clusters of cells. This is certainly influenced by the choice of J and Pb rules and should parallel some physical properties. Other attributes that can be measured and used to link with physical properties include the average number of joined faces of a molecule and the number of free cell faces. Each of these attributes has been exploited for their ability to relate to the physical properties. The choice of J and Pb rules, therefore, must be made with some attention to their attributes produced and their ability to mirror physical properties as a function of systematic rule changes. [Pg.46]

Another approach to get new liquid crystals is the lateral fluorination of the stilbazole ligands,337 which is a common and highly effective tool to exert control over mesomorphism, crystal phase stability, and physical properties. Other modifications include the use of more alkoxy substituents and other alkyl sulfate anions.338-344 Ionic silver amino complexes also display liquid crystalline behavior at rather low temperatures they are of the form [Ag(NH2 -CJl +OJX (X = N03, n = 6,8,10,12,14 X = BF4, = 8,10,12,14).345... [Pg.926]

Organic photochromic systems have actual applications in variable transmission optical materials, authentication systems and novelty items. In addition, they offer great potential in erasable optical memories and many other fields where reversible changes of physical properties other than color are wanted. The domain is interdisciplinary and expanding. [Pg.389]

Two enantiomers have identical physical properties (other than the sign of specific rotation). Thus, their IR spectra are also identical. [Pg.281]

This chapter deals with chemical and physical properties other than ones for which the nature of the hydration products must be considered, which are treated in Chapters 5 to 8. In general, properties of the whole clinker or cement are alone considered, those of the constituent phases having been dealt with in Chapter 1, but factors affecting the reactivities of these phases are included as a link with the following chapters on hydration. [Pg.96]

What we are concerned with at this time is an explanation on chemical grounds of the important fact that three amyl alcohols or pentanolSf are known all of which possess the same structural formula viz., 2-methyl butanol-i and that one of these compounds is dextrorotatory another is levo-rotatory and the third one is inactive. These three are different individual compounds with practically the same physical properties other than optical. The inactive variety of 2-methyl butanol-1 differs, however, from the other seven structurally isomeric pentanols which are likewise inactiye not only in its structure but also in the fact that by means of certain reactions there may be obtained from it both the dextro-rotatory and the levo-rotatory compounds. In it, and in other inactive compounds of the same kind, there are present equivalent amounts of the two oppositely active compounds,... [Pg.88]

Sodium pertechnetate Tc-99m was introduced for scanning the thyroid (Harper 1964) and for brain scanning (McAfee et al. 1964 Quinn 1965), primarily because of its physical properties other applications followed (Harper et al. 1966). The striking similarity of the heptavalent anion with iodide, however, has made pertechnetate an excellent radionuclide for thyroid scanning and for the study of thyroid physiology (Andros et al. 1965 Kusic et al. 1990). [Pg.174]

Since the term photochromism applies only to photophysical phenomena related to the reversible change in color triggered by light, a new denomination had to be found for molecules which show a reversible response to photoirradiation by a change in a chemical function or in a physical property other than color. They were named photoresponsive molecules. By analogy, photoresponsive polymers are polymers which undergo a change in various properties and functions upon photoirradiation. [Pg.90]

A gas supply and pump or flow regulator usually make up the source when a GC-like set-up is being used. The most common mobile phase for SFC is carbon dioxide this is based on its low cost, low interference with chromatographic detectors and good physical properties. Other examples include nitrous oxide and ammonia. Supercritical fluids can... [Pg.100]

These are orders of magnitude for comparison, not design figures. They are based on air and water physical properties. Other considerations such as heat transfer, materials of construction, suspended solids, hazardous liquids or gases (requiring low inventory) must obviously be taken into account. [Pg.325]

If the atomic volumes of the elements were plotted against the atomic weights, a series of waves was produced, rising to sharp peaks at the alkali metals sodium, potassium, rubidium, and cesium. Each fall and rise to a peak corresponded to a period in the table of elements. In each period a number of physical properties other than atomic volume also fell and rose. (See Figure 15.)... [Pg.131]

This is actually not quite right. Because M is multiply realizable, M could have occurred even if P had not occurred in the case where some physical property other than P instantiated M. So M could have had a different supervenience base other than P, say P2. The point is that M needs some sort of physical supervenience base to instantiate it and cannot occur independently of its supervenience base. Whatever supervenience base does instantiate M, it will be related to M by supervenience, and it and M will not be independent of one another. [Pg.40]

This section deals with the physical properties (other than the crystal structures and phase relationships which were discussed previously) of the allotropes a-, /3- and y-Ce. Because of the paucity of information little or nothing will be discussed about the properties of the allotropic phases S-, a - and a"-Ce. Much of the published information on the properties of a-, /3-, and y-Ce at low temperatures (< 273 K) and low pressures (< 0.5 GPa) will be ignored primarily because the measurements were made on samples containing two or three phases and the data are difficult to partition uniquely into the contributions of the individual phases. Even in cases where careful attempts were made to extract useful data the-information was ambiguous and generally not meaningful. [Pg.356]

Method Applicability Bubble size Gas hold-up Physical properties Other notifications... [Pg.775]

Chirality is a necessary, but not sufficient, condition for optical activity to be measured. If a solution contains equal numbers of right-handed and left-handed molecules, they rotate the plane-polarized light to an equal and opposite extent, so that no net rotation is observed. This mixture is called a racemate, or racemic mixture (Latin, racemus, a bunch of grapes, because Pasteur first isolated racemic tartaric acid from wine), and is sometimes designated ( ) to indicate that there are equal amounts of (+) and (-) material. Between an equal mixture and a pure enantiomer, every other mixture is also possible. We therefore define the term optical purity or enantiomer excess (ee, 7.2). If we have a mixture of 75 % of the (+)-enantiomer and 25 % of the (-)-enantiomer, we say that the optical purity is 50 %. Although the physical properties, other than optical rotation, of the two enantiomers are identical, it is not invariably the case that a racemate has exactly the same physical properties as a pure enantiomer. For example, either pure enantiomer of lactic acid melts at 53 °C but a racemic mixture melts at 16.4 °C. [Pg.238]

Consider 7.53 and its enantiomer ent-7.53. These are clearly related as object and mirror image and, in the enantiomer, chiraUty, is reversed at each of the two asymmetric carbon atoms. What is the relationship between these two molecules and the enantiomeric pair 7.54 and ent-7.54 Remembering what we said about stereoisomers at the start of the chapter, the relationship between 7.53 and 7.54 is that of diastereoisomers—all relationships that are not enantiomeric are diastereo-isomeric. Diastereoisomers are different compounds, with different chemical and physical properties. Enantiomers have the same physical properties other than their ability to rotate the plane of plane-polarized light and the same chemical reactivity unless they are reacting with a chiral reagent. [Pg.244]

During the rapid development of fullerene chemistry, many types of polymeric derivatives have been prepared. Numerous chapters and reviews have been pub-Ushed on fullerenes [9] some focus on their physical properties, others on their synthesis. Our aim here to give a detailed account of progress, especially recent... [Pg.147]


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See also in sourсe #XX -- [ Pg.118 , Pg.119 , Pg.119 ]




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Anisotropy other physical properties

Correlation of Coupling Constants with Other Physical Properties

Mechanical Measurements Combined with Other Physical Properties

Other Derived Physical Properties

Other Physical Chemical Properties of Miscible Blends

Other Physical Properties

Other Physical Properties of Stereoisomers

Other Physical-Chemical Properties

Other properties

Spectroscopic and Other Physical Properties

The Spectrum and Other Physical Properties

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