Carbon chemical properties

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... 

Oxygen is the most abundant element on earth The earths crust is rich in carbonate and sili cate rocks the oceans are almost entirely water and oxygen constitutes almost one fifth of the air we breathe Carbon ranks only fourteenth among the elements in natural abundance but trails only hydro gen and oxygen in its abundance in the human body It IS the chemical properties of carbon that make it uniquely suitable as the raw material forthe building blocks of life Let s find out more about those chemi cal properties... 

In the preceding chapter you learned that nucleophilic addition to the carbonyl group IS one of the fundamental reaction types of organic chemistry In addition to its own reactivity a carbonyl group can affect the chemical properties of aldehydes and ketones m other ways Aldehydes and ketones having at least one hydrogen on a carbon next to the carbonyl are m equilibrium with their enol isomers... 

The chemical properties of isopentenyl pyrophosphate and dimethylallyl pyrophosphate are complementary m a way that permits them to react with each other to form a carbon-carbon bond that unites two isoprene units Using the tt electrons of its double... 

Substitutive Nomenclature. The first step is to determine the kind of characteristic (functional) group for use as the principal group of the parent compound. A characteristic group is a recognized combination of atoms that confers characteristic chemical properties on the molecule in which it occurs. Carbon-to-carbon unsaturation and heteroatoms in rings are considered nonfunctional for nomenclature purposes. 

Traditional adsorbents such as sihca [7631 -86-9] Si02 activated alumina [1318-23-6] AI2O2 and activated carbon [7440-44-0], C, exhibit large surface areas and micropore volumes. The surface chemical properties of these adsorbents make them potentially useful for separations by molecular class. However, the micropore size distribution is fairly broad for these materials (45). This characteristic makes them unsuitable for use in separations in which steric hindrance can potentially be exploited (see Aluminum compounds, aluminum oxide (ALUMINA) Silicon compounds, synthetic inorganic silicates). 

Chemical Properties. The chemistry of ketenes is dominated by the strongly electrophilic j/)-hybridi2ed carbon atom and alow energy lowest unoccupied molecular orbital (LUMO). Therefore, ketenes are especially prone to nucleophilic attack at Cl and to [2 + 2] cycloadditions. Less frequent reactions are the so-called ketene iasertion, a special case of addition to substances with strongly polarized or polarizable single bonds (37), and the addition of electrophiles at C2. For a review of addition reactions of ketenes see Reference 8. 

Fibers. The principal type of phenoHc fiber is the novoloid fiber (98). The term novoloid designates a content of at least 85 wt % of a cross-linked novolak. Novoloid fibers are sold under the trademark Kynol, and Nippon Kynol and American Kynol are exclusive Hcensees. Novoloid fibers are made by acid-cataly2ed cross-linking of melt-spun novolak resin to form a fuUy cross-linked amorphous network. The fibers are infusible and insoluble, and possess physical and chemical properties that distinguish them from other fibers. AppHcations include a variety of flame- and chemical-resistant textiles and papers as weU as composites, gaskets, and friction materials. In addition, they are precursors for carbon fibers. 

Chemical Properties The formation of salts with acids is the most characteristic reaction of amines. Since the amines are soluble in organic solvents and the salts are usually not soluble, acidic products can be conveniendy separated by the reaction with an amine, the unshared electron pair on the amine nitrogen acting as proton acceptor. Amines are good nucleophiles reactions of amines at the nitrogen atom have as a first step the formation of a bond with the unshared electron pair of nitrogen, eg, reactions with acid anhydrides, haUdes, and esters, with carbon dioxide or carbon disulfide, and with isocyanic or isothiocyanic acid derivatives. 

Chemical Properties. Anhydrous sodium sulfite is stable in dry air at ambient temperatures or at 100°C, but in moist air it undergoes rapid oxidation to sodium sulfate [7757-82-6]. On heating to 600°C, sodium sulfite disproportionates to sodium sulfate and sodium sulfide [1313-82-2]. Above 900°C, the decomposition products are sodium oxide and sulfur dioxide. At 600°C, it forms sodium sulfide upon reduction with carbon (332). 

Chemical Properties. Ammonium thiocyanate rearranges upon heating to an equiHbrium mixture with thiourea 30.3 wt % thiourea at 150°C, 25.3 wt % thiourea at 180°C (373,375). At 190—200°C, dry ammonium thiocyanate decomposes to hydrogen sulfide, ammonia, and carbon disulfide, leaving guanidine thiocyanate [56960-89-5] as a residue. Aqueous solutions of ammonium thiocyanate are weakly acidic a 5 wt % solution has a pH of 4—6. 

The chemical properties of organosulfur, organoselenium, and organoteUurium compounds are markedly similar. Because bond stabUity with carbon decreases with the increasing atomic number of the element, thermal stabUity decreases, whereas oxidation susceptibUity increases to such an extent that alkyl teUurides are oxidized rapidly by air at room temperature. As a result, less has been written concerning the chemistry of organoteUurium than organoselenium compounds. Nevertheless, a sizable Uterature exists (29,55—59). 

Chemical Properties. The most impoitant reactions which tetraorganotins undergo are heterolytic, ie, electrophilic and nucleophilic, cleavage and Kocheshkov redistribution (81—84). The tin—carbon bond in tetraorganotins is easily cleaved by halogens, hydrogen hahdes, and mineral acids ... 

With minor exceptions the requirements for the physical and chemical properties of asphalt were essentially the same for the three national specifications and included penetration and ductiUty at 25 °C flash point % loss at 163 °C penetration of residue as a % of original solubiUty in carbon disulfide solubiUty in carbon tetrachloride specific gravity at 25°C and softening point. 

Because of their unique combination of physical and chemical properties, manufactured carbons and graphites are widely used in several forms in high temperature processing of metals, ceramics, glass, and fused quartz. A variety of commercial grades is available with properties tailored to best meet the needs of particular appHcations (45). Industrial carbons and graphites are available in a broad range of shapes and sizes. 

Branched-chain acids contain at least one branching alkyl group attached to the carbon chain, which causes the acid to have different physical, and in some cases different chemical, properties than their corresponding straight-chain isomers. For example, stearic acid has a melting point of about 69°C, whereas isostearic acid has a melting point of about 5°C. Some properties of commercial branched-chain acids are shown in Table 1 (1,2). 

Chemical Properties. Neopentanoic acid [75-98-9] undergoes reactions typical of carboxyUc acids. Reactions often proceed less readily than with straight-chain acids because of the steric hindrance around the carbonyl group. However, this steric hindrance at the a-carbon results ia derivatives that are typically more resistant to hydrolysis and oxidation. 

The physical and chemical properties of chlorinated paraffins are deteanined by the carbon chain length of the paraffin and the chlorine content. This is most readily seen with respect to viscosity (Fig. 1) and volatiUty (Fig. 2) increasing carbon chain length and increasing chlorine content lead to an increase in viscosity but a reduction in volatiUty. 

Color Concentrates. Color concentrates have become the method of choice to incorporate colorants into resins. Color concentrates have high ratios of colorant to a compatible vehicle. The colorant may be added at 70% colorant to 30% vehicle in a titanium dioxide mixture whereas the ratio may be 15% colorant to 85% vehicle in a carbon black mixture. The amount of colorant that can be added is dependent on the surface area and the oil absorption of the colorant and the wetting abiHty of the vehicle. The normal goal is to get as much colorant in the concentrate as possible to obtain the greatest money value for the product. Furthermore, less added vehicle minimizes the effect on the physical or chemical properties of the resin system. 

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