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Additives ozone

Ozone is a highly reactive molecule composed of three atoms of oxygen. Ozone concentrations vary by geographical location and by altitude. In addition, ozone exerts a different climate-forcing effect, depending upon altitude. [Pg.243]

The toxic effects of ozone in plant systems have been studied for some time, yet the actual mechanisms of injury are not fully understood. In addition to visible necrosis which appears largely on upper leaf surfaces, many other physiological and biochemical effects have been recorded ( ). One of the first easily measurable effects is a stimulation of respiration. Frequently, however, respiration may not increase without concomitant visible injury. Furthermore, photosynthesis in green leaves as measured by CO2 assimilation, may decrease. It is well known that ozone exposure is accompanied by a dramatic increase in free pool amino acids ( ). Ordin and his co-workers ( ) have clearly shown the effect of ozone on cell wall biosynthesis. In addition, ozone is known to oxidize certain lipid components of the cell ( ), to affect ribosomal RNA (16) and to alter the fine structure of chloroplasts (7 ). [Pg.8]

Analogous approaches to assessing VOC reactivities have been developed by Derwent and co-workers (e.g., see Hough and Derwent, 1987 Derwent and Jenkin, 1991 and Derwent et al., 1996) where a trajectory model is used to calculate the additional ozone production due to the addition of a particular VOC under conditions typical of air masses advected across northwest Europe toward the British Isles. The photochemical ozone creation potential (POCP) index thus calculated is a measure of the reactivity of the particular VOC in terms of 03 formation. Andersson-Skold and co-workers (1992) followed a similar approach for the summer conditions in southern Sweden. [Pg.913]

For the experimenter in the laboratory, not only do materials have to be chosen on the basis of their corrosion-resistance, but also for their effect on ozone decay. Some metals (e. g. silver) or metal seals enhance ozone decay considerably. This can be especially detrimental in drinking water and high purity water (semiconductor) ozone applications, causing contamination of the water as well as additional ozone consumption. Moreover, the latter will cause trouble with a precise balance on the ozone consumption, especially in experiments on micropollutant removal during drinking water ozonation. With view to system cleanliness in laboratory experiments, use of PVC is only advisable in waste water treatment, whereas quartz glass is very appropriate for most laboratory purposes. [Pg.53]

A third issue is the estimates of ozone loss associated with the polar vortex. Will the Antarctic ozone hole expand and will the Arctic ozone hole begin Can the loss of ozone be better quantified, and what are the zonal asymmetries in the CIO and BrO fields How much additional ozone is lost when the polar vortex breaks up ... [Pg.189]

At the present time there is no experimental or theoretical evidence which would support a photon chain mechanism. However, if reaction (30) does occur, the spectral and photochemical evidence is that the next reaction should be the transfer to 3nu or some other repulsive state, as discussed in Part II. Two O(3P) atoms would then be formed by predissociation. The reaction (28) would then decompose two additional ozone molecules. A quantum yield of four could then be achieved without invoking either a photon or energy chain. In view of the uncertainty of the quantum yields greater than two and the maximum reported yield of six, this mechanism is perhaps the simplest necessary to explain the reasonably acceptable experimental evidence. [Pg.59]

As for lo, the surfaces of Ganymede and Callisto are intimately connected to both radiation and atmospheric processes. Optical spectra have identified molecular oxygen in a condensed state, trapped in the ices on both satellites, as well as Europa. The characteristics of this oxygen component have been attributed to interaction with the plasma environment (Calvin and Spencer, 1997 Spencer and Calvin, 2002 Spencer et al., 1995) and may be related to the processes controlling the formation and distribution of carbon dioxide discussed above. In addition, ozone has been detected on Ganymede and attributed to the presence of micro-atmospheres of O2 and O3 trapped in the ice (Noll et al., 1996). [Pg.640]

The conversion of NO into NO2 is the characteristic step that leads to ozone formation, and the rate of conversion of NO to NO2 is often used to represent the ozone formation rate. The process does not remove either OH or NO from the atmosphere, so that the OH and NO may initiate additional ozone-forming reactions. [Pg.4956]

Pyridine oxide was shown to bind large quantities of ozone, from which all of the pyridine oxide could be recovered by addition of methanol. This apparently accounts for the additional ozone required for the ozonolysis when pyridine is present. Unfortunately, pyridine oxide could not be demonstrated in the reaction mixture. It was shown, however, in a separate experiment that pyridine oxide reacted readily with bisnoraldehyde at room temperature. The isolation was not attempted at —78°C. [Pg.166]

Treatment of Lamffill Leachates. Landfill leachate contains large quantities of nonbiodegradable and toxic constituents. Some heterogenous catalytic ozonation processes (Ecoclear or Catazone systems) can successfully treat landfill leachates. " In addition, ozone-based AOPs have also been successfully used to remove COD or TOC either as pretreatment or at the final stage of the treatment. Both heterogenous catalytic ozonation and the AOP processes are introduced below. [Pg.1997]

Scheme 2.126 Preparation of trifluoromethyltrimethyl silane (MejSiCFj, Ruppert s Reagent). Ruppert s original method [2c] above) leads, after aqueous work-up, to the formation of stoichiometric amounts of the carcinogenic HMPA (OP(NMe2)3). In addition, ozone-depleting CFjBr is used as the starting material. A recent method beloiv), with potential for technical upscale, utilizes the inexpensive CHF, and depends on a catalytic cycle initiated by diphenyldisulfide [69]. Scheme 2.126 Preparation of trifluoromethyltrimethyl silane (MejSiCFj, Ruppert s Reagent). Ruppert s original method [2c] above) leads, after aqueous work-up, to the formation of stoichiometric amounts of the carcinogenic HMPA (OP(NMe2)3). In addition, ozone-depleting CFjBr is used as the starting material. A recent method beloiv), with potential for technical upscale, utilizes the inexpensive CHF, and depends on a catalytic cycle initiated by diphenyldisulfide [69].
As a fourth step, discussion continues for the introduction of emission limits for other exhaust gas components, and for particulate matter of diesel powered vehicles. For example, there has been discussion in the USA and some European countries on separate - additional - emission limits for carbon dioxide, benzene and/or aldehydes. In the USA there is a project to consider an additional ozone-formation factor to be allocated to the tailpipe emission of passenger cars. This is because each exhaust gas component has a different potential to contribute to atmospheric ozone formation. This potential is quantified according to the theory of Carter by the maximum incremental reactivity (MIR) factor, expressed as grams of... [Pg.5]

Many different types of volatile organic compounds (VOCs) are emitted into the atmosphere, where they can affect photochemical ozone formation and other measures of air quality. Because they can react in the atmospheres at different rates and with different mechanisms, the different types of VOCs can vary significantly in their effects on air quality. The effect of a VOC on ozone formation in a particular environment can be measured by its incremental reactivity , which is defined as the amount of additional ozone formed when a small amount of the VOC is added to the environment, divided by the amount added. Although this can be measured in environmental chamber experiments, incremental reactivities in such experiment cannot be assumed to be the same as incremental reactivities in the atmosphere (Carter and Atkinson, 1989 Carter et al, 1995). This is because it is not currently practical to duplicate in an experiment all the environmental factors that affect relative reactivities and, even if it were, the results would only be applicable to a single type of environment. The only practical means to assess atmospheric reactivity, and how it varies among different environments, is to estimate its atmospheric ozone impacts using airshed models. [Pg.231]

This is known as a 1,3-dipolar addition (ozone is a 1,3-dipole)... [Pg.93]

Until about 1964, the Chapman mechanism was thought to be the principal set of reactions governing ozone formation and destruction in the stratosphere. First, improved measurement of the rate constant of reaction 4 (above) indicated that the reaction is considerably slower than previously thought, leading to larger abundances of 03 as predicted by (5.10)—(5.12). Then, measurements indicated that the actual amount of ozone in the stratosphere is a factor of 2 less than what is predicted by the Chapman mechanism with the more accurate rate constant of reaction 4 (Figure 5.5). It was concluded that significant additional ozone destruction pathways must be present beyond reaction 4. [Pg.150]

Hypobromite ion can be further oxidised with additional ozone to bromate ion... [Pg.340]

In addition, ozone treatment can be used in combination with UV exposure to samtize or disinfect a variety of substances [99, 100, 194—197]. Another application of EDL (containing Hg, Cd-Ar, or Kr) for disinfection of aqueous solutions has recently been reported by Michael [198]. [Pg.890]

Effect of energy transfer from vibrational excitation to electronical excited molecular states and directly to ozone synthesis. Additional ozone synthesis, specifically in the streamer channels, can take place via the direct use of vibrational energy. In the case of pulsed... [Pg.398]

The environment in which an article is used may influence bond durability (see also Durability fundamentals). Atmospheric ozone can cause time-dependent crack growth in vulcanized elastomers in addition, ozone can induce failure at a bond with certain bonding agents. Although water is only slightly soluble, it can permeate elastomers by an osmotic mechanism induced by salt-Uke impurities. As a result, the uptake in salt water is generally less than that in pure water. Rubber to metal bond failure has been found to occur in a time-dependent manner under salt water in the presence of electrochemical activity but much more slowly, if at all, in its absence (see also Cathodic disbondment). In the absence of imposed electrochemical activity, effects are likely to depend particularly on the metal used and its corrosion resistance. Provision of a bonded rubber cover layer over all metal surfaces subject to immersion is likely to enhance bond durability. [Pg.416]

In the upper atmosphere (the stratosphere), ozone is beneficial because it protects us from harmful ultraviolet radiation that comes from the Sun. However, in the lower atmosphere, ozone irritates the eyes and respiratory tract, which causes coughing and decreased lung function. In addition, ozone causes fabric to deteriorate and rubber to crack it also damages trees and crops. [Pg.249]


See other pages where Additives ozone is mentioned: [Pg.490]    [Pg.495]    [Pg.54]    [Pg.481]    [Pg.476]    [Pg.252]    [Pg.232]    [Pg.64]    [Pg.1192]    [Pg.1192]    [Pg.13]    [Pg.4954]    [Pg.4955]    [Pg.4963]    [Pg.849]    [Pg.700]    [Pg.392]    [Pg.319]    [Pg.704]    [Pg.3517]    [Pg.776]    [Pg.776]    [Pg.458]    [Pg.835]    [Pg.415]    [Pg.416]    [Pg.424]    [Pg.30]   
See also in sourсe #XX -- [ Pg.333 , Pg.334 , Pg.335 , Pg.336 , Pg.337 , Pg.338 , Pg.339 , Pg.340 ]




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Additivity towards ozone

Alcohols, from addition ozone

Electrophilic addition ozone

Ozone addition

Ozone addition

Ozone additive compounds

The Addition of Ozone to an Alkene Ozonolysis

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