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Free-radical molecules

In reality, many other chemical and photochemical processes take place leading to a sort of steady-state concentration of O3 which is a sensitive function of height. To be accurate, it is necessary to include the reactions of nitrogen oxides, chlorine- and hydrogen-containing free radicals (molecules containing an unpaired electron). However, occurrence of a layer due to the altitude dependence of the photochemical processes is of fundamental geochemical importance and can be demonstrated simply by the approach of Chapman (1930). [Pg.137]

We also note that some of the products are stable molecules (CH4, CO, and C2H6), while others are free-radical molecules (CH3-, CH3CO-, and CHO-), which are highly unstable and will quickly react with most stable molecules in the system or with other radical species whenever they collide. We will write dots in the symbols for these molecules to indicate that they have an unpaired electron. [Pg.400]

FLAVONOIDS Chemical compounds found in many herbal drugs. Flavonoids may help fight off infections and clear the body of harmful free radical molecules. [Pg.226]

Emission spectroscopy and, to a lesser degree, absorption spectroscopy have provided considerable information on and insight into the chemistry occurring during the process of combustion. In particular, many of the transient free-radical molecules important in the chain reactions were identified and characterized through their emission spectra in flames. Now, new laser spectroscopic techniques offer the promise of obtaining more detailed and precise information, especially for the ground electronic states of many of the molecules involved in combustion. [Pg.1]

It is equally difficult to arrive at concrete conclusions concerning the functionality of humic substances based on their ESR spectra. When compared to the ESR spectra of discrete free radical molecules, the ESR spectra are seen to be exceedingly crude. In addition, the ESR spectrum results from only a very small fraction of the molecules present in the system, further complicating any interpretation. The ESR spectra of humic substances have been interpreted in terms of the presence of semiquinone moieties. While such interpretations are reasonable, and consistent with what is known about these substances, no definitive proof of the nature of the free radical entities in humic substances has yet been provided. [Pg.560]

Free radicals, molecules with unpaired electrons, play a large role in most reactions of alkanes, such as cracking and reformation where long-chain alkanes are converted into shorter-chain alkanes and straight-chain alkanes into branched-chain isomers. [Pg.38]

Figure 3.33 lists a recipe for emulsion polymerization of polystyrene in a water dispersion of monomer droplets and soap micelles [20]. The reaction is started by light-sensitive, water-soluble initiators, such as benzoyl peroxide. If one compares the sizes of the dispersed droplets, one notices that the small soap micelles that contain also styrene in their interior are most likely to occasionally initiate a polymerization of the monomer on absorption of a free radical. Once initiated, the reaction continues until a second free radical molecule enters the micelle. Then the reaction is terminated, until a third radical starts another molecule. Monomers continuously add to the micelles, so that the polymerization continues. Keeping the free radical generation constant, a relatively narrow molar mass distribution can be obtained. [Pg.217]

Antioxidant an-te- ak-so-dont, ian- tI- (1926) n. A substance that slows down the oxidation of oils, fats, etc., and thus helps to check deterioration antioxidants are added commercially to foods, soaps, etc. Although the term technically applies to molecules reacting with oxygen, it is often applied to molecules that protect from any free radical molecule with unpaired electrons. Chemistry encyclopedia, www. ChemistryAbout.com. A substance incorporated in a material to inhibit oxidation at normal or elevated temperatures. Antioxidants are used mainly with natural and synthetic rubbers, petroleum-based resins, and other such polymers that oxidize readily due to structural unsaturation. However, some thermoplastics, namely polypropylene, ABS, rubber-modified polystyrene, acrylic and vinyl resins, also require protection by antioxidants for some uses. There are two main classes (1) Those inhibit oxidation by reacting with chain-propagating radicals, such as hindered phenols that intercept free radicals. These are called primary antioxidants or free-radical scavengers. (2) Those decompose peroxide into non-radical and stable products examples are phosphates and various sulfur compounds, e.g., esters of thiodipropionic acid. These are referred... [Pg.60]

Second, their radical quenching activity at 515 nm against the reactive oxygen species (ROS) of the reduction after the reaction of the concentration of 300 pM a stable free-radical molecule 2,2-diphenyl-1-pictylhydrazyl (DPPH, 37) (Figure 8) at half an hour at 37 °C with these 14 compoimds (14, 24-36) was in a dose-dependent manner. Among 14 compounds (14, 24-36), 5,7-dihydroxy-2, 6-dimethoxyisoflavone (33) was the highest 84.843% radical scavenging activity (RSA), followed by tenuifone (25) 83.741% RSA, izalpinin (3,5-dihydroxy-7-methoxyflavone, 26) 76.917% RSA, irisoid A... [Pg.225]

Two PAH molecules disproportionate into one hydroaromatic molecule and one free-radical molecule. [Pg.77]

The free-radical molecules condense into larger molecular weight aromatics. [Pg.77]

A Free radicals, molecules containing unpaired electrons (represented here as X ), may attack biological molecules such as the DNA molecule depicted here. [Pg.356]

Bochinski JR, Hudson ER, Lewandowski HJ, Ye J. (2004) Cold free-radical molecules in the laboratory frame. Phys. Rev. A. 70(4) 043410. [Pg.478]

Two free radical molecules may form a covalent bond by pairing the unpaired electrons, a process known as DIMERIZATION ... [Pg.127]

The phenolic structure of primary antioxidants, such as BHA, BHT, and TBHQ, allows the donation of a proton to a free radical molecule, which regenerates the acylglyc-erol molecule and interrupts the mechanism of oxidation by free radicals. Then, the phenolic derivatives are transformed into free radicals and these radicals are self-stabilized without promoting or propagating the oxidation reaction (Ramalho and Jorge, 2006). Reactions (13.1) and (13.2) indicate the action of a primary antioxidant... [Pg.228]


See other pages where Free-radical molecules is mentioned: [Pg.181]    [Pg.272]    [Pg.256]    [Pg.121]    [Pg.49]    [Pg.1756]    [Pg.532]    [Pg.11]    [Pg.194]    [Pg.303]    [Pg.843]    [Pg.45]    [Pg.391]    [Pg.392]    [Pg.392]    [Pg.822]    [Pg.330]    [Pg.596]    [Pg.295]    [Pg.3]    [Pg.549]    [Pg.226]    [Pg.158]    [Pg.15]    [Pg.46]    [Pg.42]    [Pg.157]   
See also in sourсe #XX -- [ Pg.392 ]




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