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Organic caibon

Buesseler KO, Ball L, Andrews J, Cochran JK, Hirschberg DJ, Bacon MP, Fleer A, Brzezinski M (2001) Upper ocean export of particulate organic caibon and biogenic silica in the Southern Ocean along 170°W. Deep-Sea Res II 48 4275-4297... [Pg.488]

For heat pumps based on the exothermic oxidation reactions taking place in mine-waste tips, the longevity of the operation will be limited by the mass of reactant (sulphide or organic caibon/coal) within the waste. However, if the principles above are applied and the reaction rates within the waste deduced, the longevity of the exothermic reactants can be estimated (see, e.g., Stroinberg Banwart 1994, 1999). In practice, however, many mine-waste tips are... [Pg.508]

Not needed for nonspecific analytical methods (e.g., total organic caibon). All of the compound detected must be attributed to the target analyte unless rationale supporting an alternative has been documented, "in cases where reproducibility has been performed, intermediate precision is not needed. [Pg.355]

To this purpose, isotopic data presented in this paper were obtained from several selected Gorleben groundwaters as part of the colloid characterisation programme. The contents of major and minor ions, light isotopes ( H, H, and and the U/Th isotopes were measured. Radiocarbon and were measured in dissolved inorganic carbon (DIG), ion the humic acid (HA-colloids) and fulvic acid (FA-solution) fractions of dissolved organic caibon (DOC). The and were also determined in dissolved sulphate phase. The U/Th isotope measurements were carried out on total and surface solid phases, colloid fraction (1-1000 nm particle size, HA) and solution (<1.5 nm, FA). [Pg.220]

Lovley DR, Phillips EJP (1988) Novel mode of microbial energy metabolism Organic caibon oxidation coupled to dissimilatory reduction of iron or manganese. Appl Envl Microbio 54 1472-1480 Lovley DR, Phillips EJP, Lonergan DJ (1991) Enzymatic versus nonenzymatic mechanisms for Fe(ni) reduction in aquatic sediments. Env Sci Tech 25 1062-1067 Luther GW, III (1987) Pyrite oxidation and reduction Molecular orbital theory considerations. Geochim Cosmochim Acta 51 3193-3199... [Pg.267]

Total organic caibon Not more than 0.5 ntg/mi Cf. Tots ... [Pg.462]

Fig. 17 Toted organic caibon (TOC) content in the aqueous phase eit defined sampling intervals using ricinoleic add (RA) and oleic add (OA) as surfactants... Fig. 17 Toted organic caibon (TOC) content in the aqueous phase eit defined sampling intervals using ricinoleic add (RA) and oleic add (OA) as surfactants...
The catalysts studied were characterized using XFA, TEM, XANES, EXAFS, XPS, and liquid nitrogen physisorption methods. The total organic caibon was detected by standard methodology of chemical oxygen demand (COD). [Pg.362]

Multiple bonds aie very common in organic chemistry. Ethylene (C2H4) contains a caibon-caibon double bond in its most stable Lewis structure, and each caibon has a completed octet. The most stable Lewis structure for acetylene (C2H2) contains a caibon-caibon triple bond. Here again, the octet rule is satisfied. [Pg.14]

Organic chemists use an informal nomenclature system based on Eischer projections to distinguish between diastereomers. When the caibon chain is vertical and like substituents ar e on the sane side of the Eischer projection, the molecule is described as the erythro diastereomer. When like substituents are on opposite sides of the Eischer projection, the molecule is described as the three diastereomer. Thus, as seen in the... [Pg.301]

An ability to fonn caibon-caibon bonds is fundamental to organic synthesis. The addition of Grignaid reagents to aldehydes and ketones is one of the most frequently used reactions in synthetic organic chemistry. Not only does it pennit the extension of caibon chains, but because the product is an alcohol, a wide variety of subsequent functional group transformations is possible. [Pg.595]

Ziegler found that adding certain metals or their compounds to the reaction mixture led to the fonnation of ethylene oligomers with 6-18 caibons, but others promoted the formation of very long carbon chains giving polyethylene. Both were major discoveries. The 6-18 carbon ethylene oligomers constitute a class of industrial organic chemicals known as linear a olefins that aie produced at a rate of 3 X 10 pounds/yeai in the... [Pg.610]

Methanol, ethanol, and isopropyl alcohol aie included among the readily available stalling materials commonly found in laboratories where organic synthesis is canied out. So, too, aie many other alcohols. All alcohols of four caibons or fewer, as well as most... [Pg.624]

The value of alkyl halides as stalling materials for the prepaiation of a vaiiety of organic functional gioups has been stressed many times. In our eailier discussions, we noted that aryl halides aie nonnally much less reactive than alkyl halides in reactions that involve caibon-halogen bond cleavage. In the present chapter you will see that aiyl halides can exhibit theii own patterns of chemical reactivity, and that these reactions aie novel, useful, and mechanistically interesting. [Pg.971]

I lie follow iiig anioiig the more common organic siibst.ances I out.on siilpluii 01 sulphur and nitiogcn in addition to caibon, lu(lio . en and osyg en,... [Pg.343]

Activated caibon has been studied as a means for removal of organic molecules from waste-water by adsorption. Using the following data for benzene (A) adsorption on activated carbon (Leyva-Ramos and Geankopolis, 1994, as read from several points from a graph), determine... [Pg.223]

Theoretically, an infinite numbei of different caibon compounds can exist. Carbon atoms alone or in combination with other atoms, such as oxygen, nitrogen, etc., can join to form linear, branched, and cyclic chains of nearly any length. One, two, or three bonds may be shared between two carbon atoms. In most stable organic compounds, the total number of bonds to each carbon atom is four. [Pg.1168]

The Volume Editors have spent great time and effort in considering the format of the work. The intention is to focus on transformations in the way that synthetic chemists think about their problems. In terms of organic molecules, the work divides into the formation of carbon-caifoon bonds, the introduction of heteroatoms, and heteroatom interconversions. Thus, Volumes 1-S focus mainly on carbon-carbon bond formation, but also include many aspects of the introduction of heteroatoms. Volumes 6-8 focus on interconversion of heteroatoms, but also deal with exchange of carbon-caibon bonds for carbon-heteroatom bonds. [Pg.1021]

Several caibon-carbon bond-forming reactions involve the coupling of an organic halide (R X) with an organometallic reagent or alkene. Three useful reactions are discussed in Sections 26.1-26.3 ... [Pg.1003]

Chromatographic measurements were made for the adsorption of benzene, toluene and m-xylene on molecular sieving caibon (MSC) in supercritical fluid CO2 mixed with organics. Supercritical chromatograph packed with MSC was used to detect pulse responses of organics. Adsorption equilibria and adsorption dynamics for organics were obtained by moment analysis of the response peaks. Dependences of adsorption equilibrium constants, K., and micropote difiiisivity, D, on amount adsorbed were examined. [Pg.600]

Classical Organic Synthesis (Carbon-Caibon Bond Formation)... [Pg.3]


See other pages where Organic caibon is mentioned: [Pg.488]    [Pg.37]    [Pg.1108]    [Pg.1329]    [Pg.93]    [Pg.93]    [Pg.341]    [Pg.118]    [Pg.321]    [Pg.322]    [Pg.221]    [Pg.488]    [Pg.37]    [Pg.1108]    [Pg.1329]    [Pg.93]    [Pg.93]    [Pg.341]    [Pg.118]    [Pg.321]    [Pg.322]    [Pg.221]    [Pg.495]    [Pg.97]    [Pg.59]    [Pg.327]    [Pg.307]    [Pg.488]    [Pg.278]    [Pg.299]    [Pg.84]    [Pg.850]    [Pg.154]    [Pg.593]    [Pg.47]    [Pg.56]    [Pg.397]    [Pg.113]    [Pg.316]    [Pg.850]   


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