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Physical carbons

Chemical/Physical. Carbon dioxide, chloride, dichloromaleic, oxalic and glycolic acids, were reported as ozonation products of 2,4,5-T in water at pH 8 (Struif et al., 1978). Reacts with alkali metals and amines forming water-soluble salts (Worthing and Hance, 1991). When 2,4,5-T was heated at 900 °C, carbon monoxide, carbon dioxide, chlorine, HCl, and ojtygen were produced (Kennedy et al, 1972, 1972a). [Pg.1013]

Saito, R., and Kataura, H. 2001. Optical properties and Raman spectroscopy of carhon nanotubes. In Topics in applied physics Carbon nanotubes, eds. M. S. Dresselhaus, G. Dresselhaus, and P. Avouris, 213-46. Berlin Springer. [Pg.270]

Even dynamic measurements have been made on mixtures of carbon black with decane and liquid paraffin [22], carbon black suspensions in ethylene vinylacetate copolymers [23], or on clay/water systems [24,25]. The corresponding results show that the storage modulus decreases with dynamic amplitude in a manner similar to that of conventional rubber (e.g., NR/carbon blacks). This demonstrates the existence and properties of physical carbon black structures in the absence of rubber. Further, these results indicate that structure effects of the filler determine the Payne-effect primarily. The elastomer seems to act merely as a dispersing medium that influences the magnitude of agglomeration and distribution of filler, but does not have visible influence on the overall characteristics of three-dimensional filler networks or filler clusters, respectively. The elastomer matrix allows the filler structure to reform after breakdown with increasing strain amplitude. [Pg.4]

LEE DS, SHIN DH, LEE DU, KIM jc and CHEIGH HS, The use of physical carbon dioxide absorbents to control pressure build-up and volume expansion of kimchi packages. Journal of Food Engineering, 48, 183-188. [Pg.392]

With ligno-cellulosic products, we are not dealing with pure carbon. As a result, the needed physical carbon bed must be generated. [Pg.614]

As expected from Figure 14.6 (diagonal axis), carbon must be produced, except for the case of CCI4. Actually, carbon is seen as black color on the samples after reaction as is shown in the case of TCE (Fig. 14.5). Carbon is a key material of this reaction under an inert atmosphere, both chemically and physically. Carbon produced might help to activate the C Cl bond and maintain the nanostracmre of CaO. The surface acid site on carbon can activate the C Cl bond, as previously reported (11). Since it contains no transition metals, it is environmentally benign after use. [Pg.505]

In Physics, Carbon is the preeminent resistant structure to the phenomenon of (Bose-Einstein) condensation, while being at the base of polymeric structures ... [Pg.451]

Carbon dioxide may be present in certain natural gases in significant concentrations. If the concentration is very high, it will normally be reduced in a separate purification step before the ammonia process proper. But natural gas with up to 15-20% carbon dioxide can be used without problems as feed gas for an ammonia plant. The presence of such amounts of carbon dioxide will have an effect on the operation in several sectors of the plant, but the effect on overall energy consumption is modest, especially when a physical carbon dioxide removal process is used. A typical increase in energy consumption caused by the presence of 10% carbon dioxide is about 0.05 Gcal/MT ammonia. [Pg.263]

Gas purification is by conventional shift conversion followed by a physical carbon dioxide removal (e.g. Selexol) and final purification in a cryogenic unit. The hydrogen to nitrogen ratio of the synthesis gas at the cryogenic unit inlet is 1.0-1.8. [Pg.291]

Several revamp options are available for modification of the carbon dioxide removal section depending on the type of carbon dioxide removal process. The processes mostly used in ammonia plants are chemical absorption processes based on either hot potassium carbonate (HPC) such as Benfield, or Vetrocoke, or amine solutions such as MEA. The chemical carbon dioxide removal processes may be improved or replaced with a physical process in which the absorbent is regenerated by simply flashing off carbon dioxide. In this way the need for regeneration heat may be reduced or eliminated. A physical carbon dioxide removal system may result in energy savings of 0.01-0.35 Gcal/MT ammonia. [Pg.297]

Isoparaffins have boiling points lower than normal paraffins witTilHe same number of carbon atoms. Table 1.1 presents some physical properties of selected paraffins... [Pg.4]

The analyst now has available the complete details of the chemical composition of a gasoline all components are identified and quantified. From these analyses, the sample s physical properties can be calculated by using linear or non-linear models density, vapor pressure, calorific value, octane numbers, carbon and hydrogen content. [Pg.73]

Beyond propane, it is possible to arrange the carbon atoms in branched chains while maintaining the same number of hydrogen atoms. These alternative arrangements are called isomers, and display slightly different physical properties (e.g. boiling point, density, critical temperature and pressure). Some examples are shown below ... [Pg.91]

If produced gas contains water vapour it may have to be dried (dehydrated). Water condensation in the process facilities can lead to hydrate formation and may cause corrosion (pipelines are particularly vulnerable) in the presence of carbon dioxide and hydrogen sulphide. Hydrates are formed by physical bonding between water and the lighter components in natural gas. They can plug pipes and process equipment. Charts such as the one below are available to predict when hydrate formation may become a problem. [Pg.250]

Adsorbents such as some silica gels and types of carbons and zeolites have pores of the order of molecular dimensions, that is, from several up to 10-15 A in diameter. Adsorption in such pores is not readily treated as a capillary condensation phenomenon—in fact, there is typically no hysteresis loop. What happens physically is that as multilayer adsorption develops, the pore becomes filled by a meeting of the adsorbed films from opposing walls. Pores showing this type of adsorption behavior have come to be called micropores—a conventional definition is that micropore diameters are of width not exceeding 20 A (larger pores are called mesopores), see Ref. 221a. [Pg.669]

Such isothemis are shown in figure B 1,26.4 for the physical adsorption of krypton and argon on graphitized carbon black at 77 K [13] and are examples of type VI isothemis (figure B 1.26.3 ). Equation (B1.26.7)) further... [Pg.1872]

Figure Bl.26.4. The adsorption of argon and krypton on graphitized carbon black at 77 K (Eggers D F Jr, Gregory N W, Halsey G D Jr and Rabinovitch B S 1964 Physical Chemistry (New York Wiley) eh 18). Figure Bl.26.4. The adsorption of argon and krypton on graphitized carbon black at 77 K (Eggers D F Jr, Gregory N W, Halsey G D Jr and Rabinovitch B S 1964 Physical Chemistry (New York Wiley) eh 18).
The scope of tire following article is to survey the physical and chemical properties of tire tliird modification of carbon, namely [60]fullerene and its higher analogues. The entluisiasm tliat was triggered by tliese spherical carbon allotropes resulted in an epidemic-like number of publications in tire early to mid-1990s. In more recent years tire field of fullerene chemistry is, however, dominated by tire organic functionalization of tire highly reactive fullerene... [Pg.2408]

There is the possibility of building up an extensive systematic chemistry of compounds containing boron-nitrogen bonds, analogous to the chemistry of carbon-carbon bonds but the reactivity of the B—bond is much greater than that of the C—C bond, so that we get physical, but not chemical, resemblances between analogous compounds. [Pg.146]

Lead has only one form, a cubic metallic lattice. Thus we can see the change from non-metal to metal in the physical structure of these elements, occurring with increasing atomic weight of the elements carbon, silicon, germanium, tin and lead. [Pg.168]

A particularly good selection of physical properties may be spectra, because they are known to depend strongly on the chemical structure. In fact, different types of spectra carry different kinds of structural information, NMR spectra characterize individual carbon atoms in their molecular environment. They therefore correspond quite closely to fragment-based descriptors, as underlined by the success of approaches to predict NMR spectra by fragment codes (see Section 10.2.3). [Pg.431]

Physical Properties. All heavier than, and insoluble in water. All liquids, except iodoform, CHI3, which is a yellow crystalline solid with a characteristic odour. The remainder are colourless liquids when pure ethyl iodide, CjHjI, and iodobenzene, CjHgl, are, however, usually yellow or even brown in colour. Methyl iodide, CH3I, ethyl bromide, CgH Br, ethyl iodide, chloroform, CHCI3, and carbon tetrachloride, CCI4, have sweetish odours, that of chloroform being particularly characteristic. [Pg.390]


See other pages where Physical carbons is mentioned: [Pg.289]    [Pg.192]    [Pg.20]    [Pg.289]    [Pg.192]    [Pg.20]    [Pg.49]    [Pg.34]    [Pg.59]    [Pg.132]    [Pg.240]    [Pg.572]    [Pg.600]    [Pg.2399]    [Pg.2409]    [Pg.2422]    [Pg.2577]    [Pg.2702]    [Pg.14]    [Pg.14]    [Pg.229]    [Pg.126]    [Pg.389]    [Pg.590]    [Pg.97]    [Pg.211]    [Pg.251]    [Pg.1026]   
See also in sourсe #XX -- [ Pg.232 ]




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