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Carbon, fixed forms

Wachtcrshauser s prime candidate for a carbon-fixing process driven by pyrite formation is the reductive citrate cycle (RCC) mentioned above. Expressed simply, the RCC is the reversal of the normal Krebs cycle (tricarboxylic acid cycle TCA cycle), which is referred to as the turntable of metabolism because of its vital importance for metabolism in living cells. The Krebs cycle, in simplified form, can be summarized as follows ... [Pg.196]

The complex processes of growth, reproduction, collecting nutrition and movement, perhaps even carbon-fixing processes such as photosynthesis, have to be performed to get to the simplest life forms found in the fossil records. There can be no time to dawdle complex life was formed rapidly perhaps over a period of 100-500 million years, reaching a living form close to something that we would recognise today as a bacterium. [Pg.261]

Fixed carbon is the combustible residue left after the volatile matter is driven off. It is not all carbon. Its form and hardness are an indication of fuel coking properties and, therefore, serve as a guide in the selection of combustion equipment. Generally, fixed carbon represents that portion of fuel that must be burned in the solid state. [Pg.39]

Also included in Table 7.7 are the nitrogen fixation reactions. These are similar to the carbon fixation reactions in that they involve the conversion of an oxidized inorganic species (N2) 1° a reduced form, such as ammonium. The fixed forms of nitrogen can be taken up by plants. As with carbon fixation, this process requires an energy source in order to proceed. Some N2 fixers are photosynthetic and others use energy obtained from the oxidation of reduced inorganic compounds. [Pg.189]

Subsequent labeling experiments with 13C02 showed that the 13C02 molecule originally fixed by the starting amine was not incorporated in the final product, but rather was released when the organic carbonate was formed (Scheme 6.7). Therefore, C02 can act as a catalyst for amine methoxycarbonylation with DMC (Equation 6.9 in Scheme 6.7) [11]. The use of C02 as catalyst for Equation 6.9... [Pg.132]

Catalyst activity is also affected by carbon deposits formed by the Boudouard reaction. At usual Fischer Tropsch synthesis conditions, iron catalysts form carbides but little or no deposition of elemental carbon is observed. At temperatures exceeding 270 C carbon deposition becomes critical for the plugging of fixed bed catalyst reactors [22]. Under these conditions the catalyst particles swell upon carbon deposition and also disintegrate. [Pg.59]

Any carbon-fixing process, photoauto trophic or chemoautotrophic, would remove CO2 from the ocean and hence the atmosphere. This would require that the CO2 concentration of the atmosphere before these autotrophic processes began was considerably higher than at present. For example, Garrels et al., (1973) have estimated that in order to produce all of the ferric iron, sulfate, and free O2 that has been formed since the evolution of the earth s crust, a total of 5.9 X 10 mol of CO2 must have been depleted from the original CO2 reservoir. [Pg.236]

Moooclinic needles (lamellar twinning on 001) from water mp 357", Sublimes 290-295 . Kb at 18 L3 X IQ"1 Ka 0,9 X JO-10, Absorption spectrum Hartley, J. Chem-Soc- 87, 1803, 1810 (1905), One gram dissolves in about 2000 ml water, 150 ml boiling water, 2220 ml 95% alcohol sol in the fixed alkali hydroxides, coned acids, in about 22 parts of 20% aq tribasic sodium phosphate soln moderately sol in ammonia. Almost insol in benzene, ether, chloroform, carbon tetrachloride. Forms salts which are dec by water, and compds with bases which are more stable. [Pg.1461]

Fig. 8.31. The benzene molecule. The hybridization concept allows us to link the actual geometiy of a molecule with its electronic structure (al. The sp hybrids of the six carbon atoms form the six o CC bonds, and the structure is planar. Each caibon atom thus uses two out of its three s[7 hybrids the third one lying in the same plane protrudes toward a hydrogen atom and forms the a CH bond. In this way, each caibon atom uses its three valence electrons. The fourth one resides on the 2p orbital that is perpendicular to the molecular plane. The six 2p orbitals form six rr molecular orbitals, out of which three are doubly occupied and three are empty (b). The doubly occupied ones are shown in panel (b). The (fio of the lowest energy is an all-in-phase linear combination rf the 2p atomic orbitals (only their upper lobes are shown). The and Fig. 8.31. The benzene molecule. The hybridization concept allows us to link the actual geometiy of a molecule with its electronic structure (al. The sp hybrids of the six carbon atoms form the six o CC bonds, and the structure is planar. Each caibon atom thus uses two out of its three s[7 hybrids the third one lying in the same plane protrudes toward a hydrogen atom and forms the a CH bond. In this way, each caibon atom uses its three valence electrons. The fourth one resides on the 2p orbital that is perpendicular to the molecular plane. The six 2p orbitals form six rr molecular orbitals, out of which three are doubly occupied and three are empty (b). The doubly occupied ones are shown in panel (b). The (fio of the lowest energy is an all-in-phase linear combination rf the 2p atomic orbitals (only their upper lobes are shown). The and <fi2 correspond to higher energy and to the same energy, and have a single node (apart from the node plane of the AOs). The (ps orbital that apparently completes all combinations of single-node molecular orbitals is redundant (that is why it is in parentheses), because the orbital represents a linear combination of the fix and <p2.

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See also in sourсe #XX -- [ Pg.284 ]




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