E.s.r. studies on free radicals generated in poly[p-(2-hydroxyethoxy) benzoic acid] fibres at low temperatures

Polymer ◽  
1981 ◽  
Vol 22 (9) ◽  
pp. 1267-1271 ◽  
Author(s):  
Toshihiko Nagamura ◽  
Kenneth Lawrence DeVries
1979 ◽  
Vol 52 (4) ◽  
pp. 773-780 ◽  
Author(s):  
T. Kusano ◽  
K. Kobayashl ◽  
K. Murakami

Abstract When vulcanized natural rubbers are forced to extend in the glassy state, free radicals are produced by the scission of the primary chain. The amount of the free radicals increases with the strain. The tensile yield strain decreases with the decrease of the molecular chain length between crosslinks. This behavior is explainable on the basis of the limited chain extensibility. The extended chains are broken with further increases of the strain. The mechanically produced free radicals are quite stable below about −40°C. The crosslink density of the chain-ruptured material increases about 2∼3×10−5 mol/cm3. This fact shows that the free radicals are consumed not only by recombination but by the intermolecular reaction. In both sulfur and DCP vulcanizates, the network chains rather than the crosslinks are broken by stretching. In an air stream, some free radicals react with oxygen and others form crosslinks.


1959 ◽  
Vol 32 (1) ◽  
pp. 231-243 ◽  
Author(s):  
E. I. Tinyakova ◽  
B. A. Dolgoplosk ◽  
V. N. Reĭkh

Abstract 1. The mechanism of action of various oxidation-reduction systems containing organic reducing agents, iron salts, and oxygen, is investigated, and it is shown that in hydrocarbon media these systems are an effective source of free radicals at low temperatures. 2. The possibility of utilization of these systems for initiation of a chain process of oxidative degradation of unsaturated and some saturated polymers, at low temperatures, is shown.


HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 600b-600
Author(s):  
A.C. Purvis

It has long been observed that chilling injury of warm-season fruit and vegetables during postharvest storage as well as during early seedling growth can be mitigated by maintaining high relative humidities during the exposure to low temperatures. A strong correlation between transpiration rates and chilling injury was observed among the fruit of several PI lines of greenhouse-type and field-type Cucumis sativus L. differing in their susceptibility to chilling injury. Transpiration rates and chilling injury of the F1s from crosses between resistant and susceptible lines were intermediate. Immature fruit lost moisture at faster rates and chill injured more severely than mature fruit of the same genotype. Coatings, applied as postharvest treatments to the fruit either reduced or increased chilling injury depending on the concentration applied and whether or not they retarded or enhanced moisture loss during low temperature storage. Fruit coated with surfactant-based waxes lost more moisture and developed more chilling injury than uncoated fruit or fruit coated with carnauba wax or polyethylene emulsions. The causal relationship between transpiration at low temperatures and chilling injury is not known, primarily because the precise mechanism of chilling injury has not been unequivocally delineated. The manifestation of chilling injury, however, occurs concomitantly with an increase in respiratory rate. We have postulated that chilling injury is caused by active oxygen species generated when the mitochondrial electron transport chain is impaired. In studies with germinating seed, desiccation injury was associated with free radicals generated by mitochondria. Thus, desiccation at low temperatures may intensify respiratory activity resulting in the generation of oxygen free radicals and extensive peroxidative damage to cellular membranes and enzymes.


1961 ◽  
Vol 34 (4) ◽  
pp. 1212-1219
Author(s):  
G. H. Foxley

Abstract It is clear that the subject of polymer degradation by chemical agents is an active branch of polymer chemistry. This is reflected in the large number of patents applying to polymer degradation and no attempt has been made to include every appropriate patent. Much of the comparative work is based on equal weights, rather than equal numbers of molecules, so that the true comparisons of the efficiency of peptizers are often difficult. It has been shown that polymer degradation can proceed via several mechanisms all of which involve free radicals and the main points can be summarized as follows :— In solutions at low temperatures the initiatory free radicals come from the added peptizer such as benzoyl peroxide or bis-azoisobutyronitrile. Although oxygen accelerates the reaction, it is not essential, and there is appreciable degradation in the absence of oxygen. Thiols are active only when oxygen is present even at high temperature. This is somewhat surprising, since the rubber radicals produced by thermal scission should be just as active as those produced by mastication and be capable of reaction with thiols, and serves to emphasize the importance of the role of oxygen in peptization by thiols and disulfides. Oxygen is also necessary for degradation by redox systems and in its absence structurizing takes place. The lack of work on triphenyl methane derivatives is somewhat surprising in view of the ease with which they undergo homolysis to give free radicals. However, it is not sufficient to introduce any type of free radical and expect degradation: stabilized free radicals are the best peptizers, unstable radicals can add to olefinic bonds and cause crosslinking rather than chain scission. Squalene has been used as a model compound for the study of the reactions of natural rubber with free radicals in a similar manner to the use of methylcyclohexene as a model compound for oxidation studies. This review forms part of a dissertation submitted in partial fulfillment of the requirements for the London University M.Sc. (External) Examination.


1959 ◽  
Vol 32 (1) ◽  
pp. 244-256
Author(s):  
B. A. Dolgoplosk ◽  
E. I. Tinyakova

Abstract The following redox systems capable of initiating radical polymerizations are discussed: (1) Systems of the first type, where the reaction leads to the formation of a single radical: (a) Mechanism of action of reversible systems involving dienols and salts of metals of variable valency. (b) Mechanism of the decomposition of hydroperoxides by the action of salts of metals of variable valency in their higher oxidation states. (2) Systems of the second type, where the reaction leads to the formation of two radicals. Mechanism of action and effectiveness of systems involving hydroperoxides, quinol, and sulfite. (3) Systems of the third type, in which the formation of free radicals is not directly linked to the redox process. Mechanism of action of systems involving diazoamino compounds and “polyamine” systems. (4) Crosslinking of unsaturated polymers at low temperatures by the action of redox systems. Transition from crosslinking to destructive processes in presence of oxygen.


Sign in / Sign up

Export Citation Format

Share Document