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Organic irradiation

Coolant Organic, Irradiated a ef 200-0104 see (Acetato)pentaamminecobalt Diperchlorate 206-... [Pg.14]

In contrast, the ultrasonic irradiation of organic Hquids has been less studied. SusHck and co-workers estabHshed that virtually all organic Hquids wiU generate free radicals upon ultrasonic irradiation, as long as the total vapor pressure is low enough to allow effective bubble coUapse (49). The sonolysis of simple hydrocarbons (for example, alkanes) creates the same kinds of products associated with very high temperature pyrolysis (50). Most of these products (H2, CH4, and the smaller 1-alkenes) derive from a weU-understood radical chain mechanism. [Pg.262]

The sonochemistry of solutes dissolved in organic Hquids also remains largely unexplored. The sonochemistry of metal carbonyl compounds is an exception (57). Detailed studies of these systems led to important mechanistic understandings of the nature of sonochemistry. A variety of unusual reactivity patterns have been observed during ultrasonic irradiation, including multiple ligand dissociation, novel metal cluster formation, and the initiation of homogeneous catalysis at low ambient temperature (57). [Pg.262]

The irradiation darkening to produce black pearls is merely a charring of the organic conchiolin. [Pg.223]

Heat stabilizers protect polymers from the chemical degrading effects of heat or uv irradiation. These additives include a wide variety of chemical substances, ranging from purely organic chemicals to metallic soaps to complex organometaUic compounds. By far the most common polymer requiring the use of heat stabilizers is poly(vinyl chloride) (PVC). However, copolymers of PVC, chlorinated poly(vinyl chloride) (CPVC), poly(vinyhdene chloride) (PVDC), and chlorinated polyethylene (CPE), also benefit from this technology. Without the use of heat stabilizers, PVC could not be the widely used polymer that it is, with worldwide production of nearly 16 million metric tons in 1991 alone (see Vinyl polymers). [Pg.544]

Another method for producing petoxycatboxyhc acids is by autoxidation of aldehydes (168). The reaction is a free-radical chain process, initiated by organic peroxides, uv irradiation, o2one, and various metal salts. It is terrninated by free-radical inhibitors (181,183). In certain cases, the petoxycatboxyhc acid forms an adduct with the aldehyde from which the petoxycatboxyhc acid can be hberated by heating or by acid hydrolysis. If the petoxycatboxyhc acid remains in contact with excess aldehyde, a redox disproportionation reaction occurs that forms a catboxyhc acid ... [Pg.119]

Inferences that oxidation takes place on the photocatalyst s surface have been made (67). No such conclusions can be drawn. Similar observations have been made in homogeneous media if a bimolecular reaction between two reactants is assumed. A Langmuir-type behavior is no guarantee of a surface occurring process. A rigorous treatment (68) of the kinetics involved in the photocataly2ed oxidations of organic substrates on an irradiated semiconductor has confirmed this. [Pg.405]

Fig. 9. Initiation of epoxy cure. Irradiation of a triaryl sulfonium salt produces a radical cation that reacts with an organic substrate RH to produce a cation capable of releasing a proton. The proton initiates ring-opening polymerization. X = BF , PFg, AsFg, and SgFg. ... Fig. 9. Initiation of epoxy cure. Irradiation of a triaryl sulfonium salt produces a radical cation that reacts with an organic substrate RH to produce a cation capable of releasing a proton. The proton initiates ring-opening polymerization. X = BF , PFg, AsFg, and SgFg. ...
Hot atom reactions have also been used to label organic compounds with T. Irradiation of helium-3 with neutrons according to the nuclear reaction produces very energetic tritium atoms that can displace ordinary hydrogen in organic compounds. This procedure is not very selective, and the labeling pattern must be determined to enable the tritiated product to be used effectively as a tracer (34). [Pg.14]

Fig. 4.56. Schematic diagram of a SERS-active substrate and the measurement arrangement. Alumina nanoparticles are deposited on a glass surface and produce the required roughness. A thin silver layer is evaporated on to the nanoparticles and serves for the enhancement. Organic molecules adsorbed on the silver surface can be detected by irradiation with a laser and collecting the Raman scattered light. Fig. 4.56. Schematic diagram of a SERS-active substrate and the measurement arrangement. Alumina nanoparticles are deposited on a glass surface and produce the required roughness. A thin silver layer is evaporated on to the nanoparticles and serves for the enhancement. Organic molecules adsorbed on the silver surface can be detected by irradiation with a laser and collecting the Raman scattered light.
Since free radicals are fonned on irradiation of all organic systems [36], free radicals formed in epoxies would also lead to polymerization by an analogous mechanism. [Pg.1023]

Viruses and bacteria may be eliminated by chemical methods or by irradiation, and organic poisons may also be controlled. Inorganic matter must be removed by other means. [Pg.447]


See other pages where Organic irradiation is mentioned: [Pg.272]    [Pg.140]    [Pg.2188]    [Pg.482]    [Pg.193]    [Pg.53]    [Pg.91]    [Pg.357]    [Pg.1423]    [Pg.210]    [Pg.272]    [Pg.140]    [Pg.2188]    [Pg.482]    [Pg.193]    [Pg.53]    [Pg.91]    [Pg.357]    [Pg.1423]    [Pg.210]    [Pg.204]    [Pg.1510]    [Pg.2884]    [Pg.11]    [Pg.524]    [Pg.540]    [Pg.141]    [Pg.262]    [Pg.417]    [Pg.381]    [Pg.514]    [Pg.193]    [Pg.422]    [Pg.498]    [Pg.498]    [Pg.528]    [Pg.285]    [Pg.167]    [Pg.258]    [Pg.14]    [Pg.16]    [Pg.382]    [Pg.175]    [Pg.296]    [Pg.587]    [Pg.593]    [Pg.25]    [Pg.179]    [Pg.684]   
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7-Irradiated organic glasses, electrons

Irradiated organic liquid systems, excitation

Irradiation, organic matter removed

Microwave irradiation for accelerating organic

Organic crystals, crystal structure irradiated

Organic syntheses using microwave irradiation

Organic syntheses using microwave irradiation condensation reactions

Organic syntheses using microwave irradiation oxidation

Organic syntheses using microwave irradiation oxidation reactions

Organic syntheses using microwave irradiation reduction reactions

Organic syntheses using microwave irradiation solvents

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