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From oxygenates

Figure Bl.24.12. Elastie eross seetion of helium ions seattered from oxygen atoms. The pronouneed peak in the speetnim around 3.04 MeV represents the resonanee seattering eross seetion that is often used in deteetion... Figure Bl.24.12. Elastie eross seetion of helium ions seattered from oxygen atoms. The pronouneed peak in the speetnim around 3.04 MeV represents the resonanee seattering eross seetion that is often used in deteetion...
Anodic-stripping voltaimnetry (ASV) is used for the analysis of cations in solution, particularly to detemiine trace heavy metals. It involves pre-concentrating the metals at the electrode surface by reducmg the dissolved metal species in the sample to the zero oxidation state, where they tend to fomi amalgams with Hg. Subsequently, the potential is swept anodically resulting in the dissolution of tire metal species back into solution at their respective fomial potential values. The detemiination step often utilizes a square-wave scan (SWASV), since it increases the rapidity of tlie analysis, avoiding interference from oxygen in solution, and improves the sensitivity. This teclmique has been shown to enable the simultaneous detemiination of four to six trace metals at concentrations down to fractional parts per billion and has found widespread use in seawater analysis. [Pg.1932]

Once this reaction has been initiated, it supports the combustion of many substances since they can bum in the liberated oxygen. In this respect, it is hardly distinguishable from oxygen itself but other properties serve to distinguish the two gases (see Table 9.J). [Pg.229]

FIGURE 9 6 Conversion of an enol to a ketone takes place by way of two solvent mediated proton transfers A proton is transferred to carbon in the first step then removed from oxygen in the second... [Pg.380]

Step 2 The carbocation transfers a proton from oxygen to a water molecule yielding a ketone... [Pg.380]

The mechanism for formation of benzaldehyde diethyl acetal which proceeds m two stages is presented m Figure 17 9 The first stage (steps 1-3) involves formation of a hemiacetal m the second stage (steps 4-7) the hemiacetal is converted to the acetal Nucleophilic addition to the carbonyl group characterizes the first stage carbocation chemistry the second The key carbocation intermediate is stabilized by electron release from oxygen... [Pg.720]

Esters Like acid anhydrides the carbonyl group of an ester is stabilized by elec tron release from oxygen Because there is only one carbonyl group versus two m anhydrides esters are stabilized more and are less reactive than anhydrides... [Pg.835]

The question of whether adsorption should be done ia the gas or Hquid phase is an interesting one. Often the choice is clear. Eor example, ia the separation of nitrogen from oxygen, Hquid-phase separation is not practical because of low temperature requirements. In C q—olefin separation, a gas-phase operation is not feasible because of reactivity of feed components at high temperatures. Also, ia the case of substituted aromatics separation, such as xylene from other Cg aromatics, the inherent selectivities of iadividual components are so close to one another that a simulated moving-bed operation ia hquid phase is the only practical choice. [Pg.303]

Only the surface layers of the catalyst soHd ate generaHy thought to participate in the reaction (125,133). This implies that while the bulk of the catalyst may have an oxidation state of 4+ under reactor conditions, the oxidation state of the surface vanadium may be very different. It has been postulated that both V" " and V " oxidation states exist on the surface of the catalyst, the latter arising from oxygen chemisorption (133). Phosphoms enrichment is also observed at the surface of the catalyst (125,126). The exact role of this excess surface phosphoms is not weH understood, but it may play a role in active site isolation and consequently, the oxidation state of the surface vanadium. [Pg.454]

Oxidation of LLDPE starts at temperatures above 150°C. This reaction produces hydroxyl and carboxyl groups in polymer molecules as well as low molecular weight compounds such as water, aldehydes, ketones, and alcohols. Oxidation reactions can occur during LLDPE pelletization and processing to protect molten resins from oxygen attack during these operations, antioxidants (radical inhibitors) must be used. These antioxidants (qv) are added to LLDPE resins in concentrations of 0.1—0.5 wt %, and maybe naphthyl amines or phenylenediamines, substituted phenols, quinones, and alkyl phosphites (4), although inhibitors based on hindered phenols are preferred. [Pg.395]

Oxidation. Olefins in general can be oxidized by a variety of reagents ranging from oxygen itself to ozone (qv), hydroperoxides, nitric acid (qv), etc. In some sequences, oxidation is carried out to create a stable product such as 1,2-diols or glycols, aldehydes, ketones, or carboxyUc acids. In other... [Pg.436]

Reaction 1 is the rate-controlling step. The decomposition rate of pure ozone decreases markedly as oxygen builds up due to the effect of reaction 2, which reforms ozone from oxygen atoms. Temperature-dependent equations for the three rate constants obtained by measuriag the decomposition of concentrated and dilute ozone have been given (17—19). [Pg.491]

The calculated half-life of 1 mol % (1.5 wt %) of pure gaseous ozone diluted with oxygen at 25, 100, and 250°C (based on rate constants from Ref. 19) is 19.3 yr, 5.2 h, and 0.1 s, respectively. Although pure ozone—oxygen mixtures are stable at ordinary temperatures ia the absence of catalysts and light, ozone produced on an iadustrial scale by silent discharge is less stable due to the presence of impurities however, ozone produced from oxygen is more stable than that from air. At 20°C, 1 mol % ozone produced from air is - 30% decomposed ia 12 h. [Pg.491]

Ozone Generation from Oxygen. Oxygen is dissociated iato atoms by iaelastic coUisions with energetic electrons (6—7 eV) (89,90). [Pg.498]

Therefore, first-order, decomposition rates for alkyl hydroperoxides, ie, from oxygen—oxygen bond homolysis, are vaUd only if induced decomposition reactions... [Pg.103]

Polyamides, like other macromolecules, degrade as a result of mechanical stress either in the melt phase, in solution, or in the soHd state (124). Degradation in the fluid state is usually detected via a change in viscosity or molecular weight distribution (125). However, in the soHd state it is possible to observe the free radicals formed as a result of polymer chains breaking under the appHed stress. If the polymer is protected from oxygen, then alkyl radicals can be observed (126). However, if the sample is exposed to air then the radicals react with oxygen in a manner similar to thermo- and photooxidation. These reactions lead to the formation of microcracks, embrittlement, and fracture, which can eventually result in failure of the fiber, film, or plastic article. [Pg.230]

The oxygen reaction is quite complex. Complete reduction from oxygen gas to hydroxide ion involves four electrons and requires several steps. Initially, oxygen is reduced to peroxyl ion [14691-59-9]... [Pg.532]


See other pages where From oxygenates is mentioned: [Pg.61]    [Pg.178]    [Pg.257]    [Pg.259]    [Pg.118]    [Pg.62]    [Pg.1011]    [Pg.21]    [Pg.680]    [Pg.341]    [Pg.251]    [Pg.256]    [Pg.374]    [Pg.459]    [Pg.129]    [Pg.311]    [Pg.379]    [Pg.484]    [Pg.498]    [Pg.498]    [Pg.499]    [Pg.500]    [Pg.101]    [Pg.506]    [Pg.378]    [Pg.44]    [Pg.290]    [Pg.542]    [Pg.67]    [Pg.223]    [Pg.453]    [Pg.165]    [Pg.485]    [Pg.483]   
See also in sourсe #XX -- [ Pg.573 ]




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1,3-Migration of an aryl group from oxygen

Alcohols from alkenes by singlet oxygen oxidation

Aldehydes, acetal formation from with oxygen

Amines oxygen atom transfer from hydroperoxides

An Enzyme-bound Red Chlorophyll Catabolite from Enzymatic Oxygenation of Pheophorbide

Annihilation rate from oxygen

Azelaic Acid from Vegetable Feedstock via Oxidative Cleavage with Ozone or Oxygen

Carbon dioxide, oxygen transfer from

Cobalt hydroxide in electrochemical production of oxygen from water

Cobalt salts oxygen production from water

Departure of Anionic Oxygen Leaving Groups from Sugars

Dioxetanes, from singlet oxygen

Electrochemistry hydrogen or oxygen production from water

Electron transfer reactions oxygen production from water

Electron transfer, from ethylene oxygen

Formation of Oxygenated Products from Synthesis Gas

Formation of Ozone from Oxygen

Frostbite from oxygen

Glycoside Synthesis from 1-Oxygen-Substituted Glycosyl Imidates

Hazards from explosion oxygen

In oxygen production from water

Indoles, oxygenated, radicals from

Iron hydroxide in electrochemical production of oxygen from water

Iron, tris in photoproduction of oxygen from water

Making oxygen from water

Manganese complexes oxygen production from water

Manganese oxide catalysts, oxygen production from water

Manganese salts oxygen production from water

Metal oxides oxygen production from water

Metal oxygen transfer from ligand

Metalloporphyrins in oxygen production from water

Migration of silicon, from carbon to oxygen

Negative conjugation - donation from oxygen lone pairs to breaking bonds

Nitrate esters from the ring-opening of strained oxygen heterocycles

Nitrogen (and Oxygen) Separation from Air

Oxidative activation oxygen transfer from tert-butyl

Oxide cathodes oxygen loss from

Oxygen Atom Transfer from Coordinated Nitrite Ligands

Oxygen adsorption, from

Oxygen desorption from

Oxygen electrocatalytic oxidation from

Oxygen electrochemical production from water

Oxygen evolution from water

Oxygen evolving center from Photosystem

Oxygen exchange from

Oxygen excited, from flash photolysis

Oxygen explosions from

Oxygen from coal

Oxygen from inert gases

Oxygen from photolysis

Oxygen from photosynthesis

Oxygen from seawater

Oxygen from solvents

Oxygen from water

Oxygen generation from water

Oxygen isotopes dust from

Oxygen leakage from roots

Oxygen migration from

Oxygen ozone formation from

Oxygen pathway, from peroxide

Oxygen photoelectrochemical production from water

Oxygen photoproduction from water

Oxygen production from water

Oxygen radicals, -cleavage from peroxide decomposition

Oxygen radicals, generation from

Oxygen radicals, generation from lipids

Oxygen release from oxyhemoglobin

Oxygen removal from hydrogen

Oxygen removal from oxides

Oxygen removal from samples

Oxygen transfer from cytochrome

Oxygen, reactions with potassium from

Oxygenated mixture from pressure oxidation

Photosynthesis atmospheric oxygen from

Phthalocyanines catalysts, oxygen production from water

Platinum oxides catalysts, oxygen production from water

Polarography hydrogen or oxygen production from water

Porphyrins catalysts, oxygen production from water

Radicals from Oxygen Heterocycles

Radicals from Oxygenated Furans

Radicals from Oxygenated Pyrans

Reactions oxygen transfer from nitrosyl ligands

Reactive oxygen , superoxide anion radical produced from

Reagents Derived from Hydrogen and Oxygen

Ruthenium oxide catalysts, oxygen production from water

Ruthenium oxide hydrogen and oxygen production from water

Singlet oxygen from endoperoxides

Singlet oxygen from hydrogen peroxide

Singlet oxygen from triphenyl phosphite ozonide

Sodium hypochlorite, singlet oxygen from

Superoxide from oxygen

Synthesis of Oxygenates from Syngas by Homogeneous Catalysts

Temperature samples quenched from oxygen

Unsubstituted Triorganotin Carboxylates Derived from Oxygen and Sulfur Containing Acids

Vinyl acetate oxygen removal from

Water from gaseous hydrogen and oxygen

Zinc, bis in electrochemical production of hydrogen or oxygen from water

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