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Chemical Transformation and Degradation

In addition to the quinolylimidazole alkaloids previously isolated a reinvestigation served to reveal the presence of three new alkaloids of the same general type. Spectral methods were the source of most of the structural information of these bases but chemical transformations and degradations proved decisive in distinguishing between alternatives. [Pg.540]

Kekule was the first to recognize that these early aromatic compounds all contain a six-carbon unit and that they retain this six-carbon unit through most chemical transformations and degradations. Benzene was eventually recognized as being the parent compound of this... [Pg.634]

L. Y. Young and C. E. CemigUa, eds.. Microbial Transformation and Degradation of Toxic Organic Chemicals, WUey-Liss, New York, 1995. [Pg.41]

Findlay M, S Fogel, L Conway, A Taddeo (1995) Field treatment of coal tar-contaminated soil based on results of laboratory treatment studies. In Microbial transformation and degradation of toxic organic chemicals (Eds LY Young, CE Cerniglia), pp. 487-513. Wiley-Liss, New York. [Pg.655]

Degradation is often the result of the combined effect of chemical transformation and biodegradation. For example, the oxidation/reduction of complex hydrocarbons can produce simple compounds such as peroxides, primary alcohols, and monocarbocylic acids. These compounds can then be further degraded by bacteria, leading to the formation of carbon dioxide, water, and new bacterial biomass.19-35... [Pg.704]

Sutherland JB, Rafii F, Khan AA et al (1995) Mechanisms of polycyclic aromatic hydrocarbon degradation. In Young LY, Cemiglia CE (eds) Microbial transformation and degradation of toxic organic chemicals. Wiley, New York... [Pg.423]

As a first approximation, we consider the main subsurface transformation processes to comprise reactions leading to chemical transformation or degradation and metabolite formation in the liquid phase or the solid-liquid interface and reactions resulting in complexation of chemicals, which in turn lead to a change in their physicochemical properties. [Pg.271]

Swoboda-Goldberg, N.G. Chemical contamination of the environment sources, types, and fate of synthetic organic chemicals. In Microbial Transformation and Degradation of Toxic Organic Chemicals Young, L.Y., Cemiglia, C., Eds. Wiley-Liss NY, 1995 27-74. [Pg.163]

Due to the fact that industrial composites are made up of combinations of metals, polymers, and ceramics, the kinetic processes involved in the formation, transformation, and degradation of composites are often the same as those of the individual components. Most of the processes we have described to this point have involved condensed phases—liquids or solids—but there are two gas-phase processes, widely utilized for composite formation, that require some individualized attention. Chemical vapor deposition (CVD) and chemical vapor infiltration (CVI) involve the reaction of gas phase species with a solid substrate to form a heterogeneous, solid-phase composite. Because this discussion must necessarily involve some of the concepts of transport phenomena, namely diffusion, you may wish to refresh your memory from your transport course, or refer to the specific topics in Chapter 4 as they come up in the course of this description. [Pg.269]

The structures of the compounds were elucidated by a combination of NMR techniques (lH-, 13C-, and 13C-DEPT NMR) and chemical transformation, enzymatic degradation, and as well as mass spectrometry, which gives information on the saccharide sequence. A more recent approach consists of an extensive use of high-resolution 2D NMR techniques, such as homonuclear and heteronuclear correlated spectroscopy (DQF-COSY, HOHAHA, HSQC, HMBC) and NOE spectroscopy (NOESY, ROESY), which now play the most important role in the structural elucidation of intact glycosides. These techniques are very sensitive and non destructive and allow easy recovery of the intact compounds for subsequent biological testing. [Pg.37]

Figure 10.9—Schematic diagram of various infrared spectrometers, a) Single beam model its principle is still used for measurements at a single wavelength b) double beam model c) single beam Fourier transform instrument. Contrary to UV/VIS spectrometers, the sample is placed immediately after the light source. Since photon energy in this range is insufficient to break chemical bonds and degrade the sample, it can be permanently exposed to the full radiation of the source. Figure 10.9—Schematic diagram of various infrared spectrometers, a) Single beam model its principle is still used for measurements at a single wavelength b) double beam model c) single beam Fourier transform instrument. Contrary to UV/VIS spectrometers, the sample is placed immediately after the light source. Since photon energy in this range is insufficient to break chemical bonds and degrade the sample, it can be permanently exposed to the full radiation of the source.

See other pages where Chemical Transformation and Degradation is mentioned: [Pg.112]    [Pg.299]    [Pg.1660]    [Pg.623]    [Pg.628]    [Pg.141]    [Pg.112]    [Pg.299]    [Pg.1660]    [Pg.623]    [Pg.628]    [Pg.141]    [Pg.140]    [Pg.154]    [Pg.316]    [Pg.188]    [Pg.2]    [Pg.125]    [Pg.494]    [Pg.836]    [Pg.400]    [Pg.462]    [Pg.126]    [Pg.301]   


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