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Hydrogen destruction

Kinetic results concerning catalytic hydrogenative destruction of heterocyclic nitrogen compounds have been published by Cox and Berg.21 In their operating condition (370°C, 17 atm, space velocity 0.5-20 h 1, which does not affect the rate of HDN, wt% N < 2.5%), they found that most of the five membered ring compounds (pyrrole derivatives and indole) follow a second-order law with respect to the amine pressure, while a first-order law is shown for six membered ring compounds (pyridine and derivatives). [Pg.133]

Valence bond and molecular orbital theory both incorporate the wave description of an atom s electrons into this picture of H2 but m somewhat different ways Both assume that electron waves behave like more familiar waves such as sound and light waves One important property of waves is called interference m physics Constructive interference occurs when two waves combine so as to reinforce each other (m phase) destructive interference occurs when they oppose each other (out of phase) (Figure 2 2) Recall from Section 1 1 that electron waves m atoms are characterized by their wave function which is the same as an orbital For an electron m the most stable state of a hydrogen atom for example this state is defined by the Is wave function and is often called the Is orbital The valence bond model bases the connection between two atoms on the overlap between half filled orbifals of fhe fwo afoms The molecular orbital model assembles a sef of molecular orbifals by combining fhe afomic orbifals of all of fhe atoms m fhe molecule... [Pg.59]

Destruction of the masking ligand by chemical reaction may be possible, as in the oxidation of EDTA in acid solutions by permanganate or another strong oxidizing agent. Hydrogen peroxide and Cu(II) ion destroy the tartrate complex of aluminum. [Pg.1170]

Charcoal Charcoal is the residue from the destructive distillation of wood. It absorbs moisture readily, often containing as much as 10 to 15 percent water. In addition, it usually contains about 2 to 3 percent ash and 0.5 to I.O percent hydrogen. The heating value of charcoal is about 27,912 to 30,238 kj/kg (12,000 to 13,000 Btu/lb). [Pg.2361]

Often contain defects (hydrogen cracks, slag inclusions, stop-start marks). Help initiate fatigue cracks. Critical welds must be tested non-destructively and defects must be gouged out. [Pg.299]

The third category for interactions is high dose (III). The effects produced by this level of interaction can be seen by the casual observer. The result of high-dose exposure is destruction or severe injury of the forest system. High-dose conditions are almost always associated with point source emissions. The pollutants most often involved are SO2 and hydrogen fluoride. Historically, the most harmful sources of pollution for surrounding forest ecosystems have been smelters and aluminum reduction plants. [Pg.120]

Although direct nitration was not possible, 2-amino-4-methylselena-zole can be directly brominated by treatment with bromine in carbon tetrachloride, the hydrogen bromide salt of 2-amino-4-methyl-5-bromoselenazole, mp 180°C (decomp.) is formed. However, all attempts to obtain the free base from this salt failed and led to complete decomposition. In this bromination, an equivalent quantity of bromine must be used excess also leads to complete destruction of the molecule. From the decomposition products an oily compound can be detected similar to bromoacetone. ... [Pg.355]

Boric acid esters provide for thermal stabilization of low-pressure polyethylene to a variable degree (Table 7). The difference in efficiency derives from the nature of polyester. Boric acid esters of aliphatic diols and triols are less efficient than the aromatic ones. Among polyesters of aromatic diols and triols, polyesters of boric acid and pyrocatechol exhibit the highest efficiency. Boric acid polyesters provide inhibition of polyethylene thermal destruction following the radical-chain mechanism, are unsuitable for inhibition of polystyrene depolymerization following the molecular pattern and have little effect as inhibitors of polypropylene thermal destruction following the hydrogen-transfer mechanism. [Pg.88]

A process petrochemical plant producing a synthesis gas high in hydrogen experiences an explosion that results in the destruction of a 1500 cubic foot storage vessel normally held at 50 psig. Unprotected glass windows (i.e., no wire mesh reinforcing, nor tempered) in the plant area 150 feet away from the tank are broken. WTiat pressures were involved ... [Pg.501]

Thermal conductivity detector. The most important of the bulk physical property detectors is the thermal conductivity detector (TCD) which is a universal, non-destructive, concentration-sensitive detector. The TCD was one of the earliest routine detectors and thermal conductivity cells or katharometers are still widely used in gas chromatography. These detectors employ a heated metal filament or a thermistor (a semiconductor of fused metal oxides) to sense changes in the thermal conductivity of the carrier gas stream. Helium and hydrogen are the best carrier gases to use in conjunction with this type of detector since their thermal conductivities are much higher than any other gases on safety grounds helium is preferred because of its inertness. [Pg.241]

The procedure is experimentally simple, and the workup involves only the destruction of the traces of hydrogen peroxide with manganese dioxide and evaporation of the hexamethyldisiloxane. Pyridine additives serve to buffer the highly acidic rhenium species and to shut down the detrimental acid-catalyzed epoxideopening pathways. The scope of this transformation is best appreciated through the examples presented in Table 12.2 [28],... [Pg.451]

The reaction takes place above 20 atms press and above 482°, with suitable H2 partial press and contact time necessary to obtain destructive hydrogenation without the formation of poly merized material. The resulting hydroformed naphthas may be halogenated, sulfonated or nitrated... [Pg.187]

Owing to the reactions of the initial primary radiolysis products among themselves, as in Eqs. (11-58)—(11-62), it is usually necessary to add another reagent to remove the unwanted ones. For example, to study reactions of e alone, one must work in neutral or basic solution to avoid its destruction by HsO+ (see Problem 11-12). Also, hydroxyl radicals and hydrogen atoms are removed from the system by prior addition of terf-butyl alcohol to give noninterfering products,... [Pg.269]

In molecular hydrogen, where we are building LCAO-MOs from two atomic orbitals, we expect two molecular orbitals. In the second molecular orbital, the two atomic orbitals interfere destructively where they overlap. This orbital has the form... [Pg.240]

Since the recognition of the role of chlorine in catalytic ozone destruction, increasing effort has been devoted to finding replacements. In most cases reported so far, the replacements are partially halogenated molecules that retain one or more hydrogen atoms (HCFCs and HFC s). The presence of H-atoms gives HO a handle (via H-atom abstractions such as R4) for their tropospheric... [Pg.80]

Under most conditions in vivo, the peroxidase activity of catalase seems to be favored. Catalase is found in blood, bone marrow, mucous membranes, kidney, and fiver. Its function is assumed to be the destruction of hydrogen peroxide formed by the action of oxidases. [Pg.88]

Fig. 4. Organics destruction efficiency with Fig. 5. The emissions of hydrogen chloride from adding Fc203 powders each MSO reactor... Fig. 4. Organics destruction efficiency with Fig. 5. The emissions of hydrogen chloride from adding Fc203 powders each MSO reactor...

See other pages where Hydrogen destruction is mentioned: [Pg.38]    [Pg.270]    [Pg.38]    [Pg.270]    [Pg.154]    [Pg.2228]    [Pg.2339]    [Pg.297]    [Pg.475]    [Pg.10]    [Pg.1025]    [Pg.14]    [Pg.20]    [Pg.84]    [Pg.85]    [Pg.88]    [Pg.851]    [Pg.804]    [Pg.419]    [Pg.245]    [Pg.390]    [Pg.619]    [Pg.16]    [Pg.96]    [Pg.208]    [Pg.371]    [Pg.762]    [Pg.840]    [Pg.866]    [Pg.248]    [Pg.62]    [Pg.578]    [Pg.580]    [Pg.68]   
See also in sourсe #XX -- [ Pg.31 ]




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Destructive hydrogenation

Hydrocarbons destructive hydrogenation

Hydrogen bomb destructiveness

Hydrogen ions acidic destruction

Hydrogen peroxide destruction

Hydrogen sulfide destructive

Hydrogenation, general destructive

The Destructive Hydrogenation of Hydrocarbons

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