Free radical-based mechanism

Irradiation effects in organic polymers result from the cleavage of chemical bonds and the subsequent reactions of intermediates generated thereby. These reactions lead to significant alterations in the physical properties of polymeric materials, and this topic has been covered in numerous books and articles [12,38-54]. As far as linear chain polymers are concerned, any changes in physical properties are due mainly to the formation of permanent main-chain scissions and intermolecular crosslinks. A general free-radical-based mechanism related to these processes is presented in Scheme 5.11. 

Additionally, organotin mercaptides can act as antioxidants, as they can sequester free-radical degradation mechanisms (48). The one drawback of mercaptide-based tin stabilizers is the discoloration of the sulfur after exposure to uv-radiation. Special precautions or formulations need to be developed for outdoor apphcations. 

Of the commercially available EB-curable adhesives [9-12], the resins fall within one of two categories based on their curing mechanisms. The majority of EB-curable resins are based on (meth)acrylate-functionalized oligomers involving a free-radical curing mechanism. The second category is the epoxy resins that cure by a cationic mechanism. 

The polymerization rate equations are based on a classical free radical polymerization mechanism (i.e., initiation, propagation, and termination of the polymer chains). 

Our acrylic polymerization model was developed to meet the need for solving these problems. Kinetics used are based on fairly well accepted and standard free radical polymerization mechanisms. 

Other very convincing evidences for free radical-mediated mechanism of decomposition and reactions of peroxynitrite and nitrosoperoxocarboxylate were demonstrated by Lehnig [140] with the use of CIDNP technique. This technique is based on the effects observed exclusively for the products of free radical reactions their NMR spectra exhibit emission characterizing a radical pathway of their formation. Lehnig has found the enhanced emission in the 15N NMR spectra of N03- formed during the decomposition of both peroxynitrite and nitrosoperoxocarboxylate. This fact indicates that N03- was formed from radical pairs [ N02, H0 ] and [ N02, C03 ]. Emission was also observed in the reaction of both nitrogen compounds with tyrosine supposedly due to the formation of radical pair [ N02, tyrosyl ]. 

The autoxidation mechanism by which 9,10-dihydroanthra-cene is converted to anthraquinone and anthracene in a basic medium was studied. Pyridine was the solvent, and benzyl-trimethylammonium hydroxide was the catalyst. The effects of temperature, base concentration, solvent system, and oxygen concentration were determined. A carbanion-initi-ated free-radical chain mechanism that involves a singleelectron transfer from the carbanion to oxygen is outlined. An intramolecular hydrogen abstraction step is proposed that appears to be more consistent with experimental observations than previously reported mechanisms that had postulated anthrone as an intermediate in the oxidation. Oxidations of several other compounds that are structurally related to 9,10-dihydroanthracene are also reported. 

In vitro tests, used in evaluation of antioxidant properties make use of the ability of antioxidants to quench free radicals. Based on this mechanism, the methods are divided into two groups SET - single electron transfer, and HAT - hydrogen atom transfer. Reactions with antioxidants in assays with the DPPH radical, ABTS and the Folin-Ciocalteu reagent both operate according to the SET and HAT mechanism. Due to the kinetics of the reaction, they are included in the... 

Resin solidification (curing) occurs by a free radical addition mechanism at the double bonds. That is why no by-products are formed. Curing compositions based on polyester resins contain a large number of different components (resins, initiators, accelerators, monomers, oligomers, fillers, etc), which may have various chemical structures, and may be used in various proportions. 

Based on these investigations, the conclusion about free radical, chain mechanism of the reaction is that its rate is mostly determined by HO radical concentration in the system [50],... 

Extensive investigations on the catalytic mechanism of classical peroxidases resulted in a consensus model involving five different iron species [30, 31], These species are ferrous, ferric, Compound I, Compound II, and Compound III (Fig. 11.1). As discussed in Chap. 5, after the reaction of ground state (GS) Femporphyrin with H202, Compound I (Cl) is formed, a cationic oxob e,vpor-phyrin-based Ji-free radical. Electron paramagnetic resonance (EPR) studies established that, in peroxidases of classes I and III, the second oxidation equivalent in Cl is present as a porphyrin-based free radical [32, 33]. In peroxidases from fungal sources, electron abstraction from the protein results in the formation of a different species with the free radical based in a residue close to the porphyrin. 

The proposed free radical chain mechanism for this reaction is given in Scheme 3. The striking catalytic effect of the metal ions such as Cu2+ and Fe3+ is attributed to their ability to accept an electron from the enamine in the chain initiation step. The autooxidation of the SchifFs bases of a,/ -unsaturated ketones is thought to proceed similarly via the enamine form of the SchifFs bases. 

Ashmore and Levitt have extended their earlier study of the NO2-H2 reaction to higher pressures over the temperature range 371-433 °C. They find clear evidence for a free radical chain mechanism based on sensitization and scavenging experiments over a range of pressures. The course of the reaction was followed by absorption measurements of the NO2 concentration. At high (= 40/1) ratios of hydrogen to nitrogen dioxide surface phenomena are not important, but at 5/1 ratios acceleration of the rate of NO2 loss occurs when the surface-to-volume ratio is increased. 

When the pyrolytic process does not occur in gas phase, different problems appear. Although equations of the type (6) with k expressed by rel. (5) or (14) can be used in certain cases, these may lead to incorrect results in many cases. Various empirical models were developed for describing the reaction kinetics during the pyrolysis of solid samples. Most of these models attempt to establish equations that will globally describe the kinetics of the process and fit the pyrolysis data. Several models of this type will be described in Section 3.3. A different approach can be chosen, mainly for uniform repetitive polymers. In such cases, a correct equation can be developed for the description of the reaction kinetics. This is based on the study of the steps occurring during pyrolysis involving a free radical chain mechanism. The subject will be discussed in some detail in Section 3.4. 

Thermal decomposition of uniform repetitive polymers was extensively studied in literature [17-19] in relation to the thermal stability of synthetic polymers. A kinetics equation has been developed based on the study of the steps occurring during pyrolysis involving a free radical chain mechanism [17]. For some natural polymers such as rubber, this theory is directly applicable. However, for non-repetitive polymers, or for polymers with more complex decomposition pathways, the theory does not provide appropriate kinetics equations. 

These reactions proceed in the absence of a reducing agent and it was proposed that they follow a free radical reduction mechanism in which the coordination of two equivalents of a strong cr-donor Lewis base causes a radical reductive loss of Cf from the Ti center (Scheme 2). This mechanism was supported by the observation that no reduced species are observed when the reactions are carried out in the presence of weaker donors such as NEt3 or PPh3. 

Radiation curable polymer systems are based on the same chemical structural design as the conventional polymer systems, but certain modifications are made in order to accommodate reactive unsaturation sites necessary for a radiation-induced free radical curing mechanism. Examples of these modifications of conventional polymer structures to form radiation curable polymers are as follows ... 

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