The Destructive Dissolution of Vulcanized Rubbers

1951 ◽  
Vol 24 (3) ◽  
pp. 616-620
Author(s):  
B. Dogadkin ◽  
Z. Tarasova

Abstract In previous work the process of destructive dissolution of vulcanized natural rubber was described, and it was shown that, in the strict absence of oxygen, a vulcanizate cannot be dissolved in a hydrocarbon medium at temperatures up to 140° C. Only in the presence of molecular oxygen does heating bring about dissolution of vulcanized rubber in the solvent, under which conditions the process proceeds along this pattern: union of oxygen with the double bonds → disintegration of the molecular chains where oxygen has combined → dissolution. if the surface area of the vulcanizate remains constant, the process takes place at a constant rate which depends on the temperature and the partial pressure of the oxygen in solution. In the following, experiments are described, the results of which show that vulcanized synthetic polymers also undergo destructive solution. The experimental method was the same as that described previously. The vulcanizates were prepared from recipes adapted to the particular synthetic rubbers. As was expected, the rate of destructive solution depends on the molecular structure of the rubbers (see Figure 1).

1963 ◽  
Vol 36 (2) ◽  
pp. 389-398 ◽  
Author(s):  
A. N. Gent

Abstract An experimental study is described of a “secondary” relaxation process in stretched vulcanizates, which becomes dominant after long periods at normal temperatures. It is shown to be affected markedly by the temperature, the atmosphere in which the test is conducted, and the presence of oxidation inhibitors. It is therefore attributed to oxidative deterioration of the molecular structure. In some vulcanizates, however, a similar or even greater relaxation is found to occur in vacuo, and this is attributed to the failure of specific crosslink structures. The extent of recovery on releasing the extended testpieces has also been investigated for a number of natural rubber vulcanizates.


Author(s):  
P. Sadhukhan ◽  
J. B. Zimmerman

Rubber stocks, specially tires, are composed of natural rubber and synthetic polymers and also of several compounding ingredients, such as carbon black, silica, zinc oxide etc. These are generally mixed and vulcanized with additional curing agents, mainly organic in nature, to achieve certain “designing properties” including wear, traction, rolling resistance and handling of tires. Considerable importance is, therefore, attached both by the manufacturers and their competitors to be able to extract, identify and characterize various types of fillers and pigments. Several analytical procedures have been in use to extract, preferentially, these fillers and pigments and subsequently identify and characterize them under a transmission electron microscope.Rubber stocks and tire sections are subjected to heat under nitrogen atmosphere to 550°C for one hour and then cooled under nitrogen to remove polymers, leaving behind carbon black, silica and zinc oxide and 650°C to eliminate carbon blacks, leaving only silica and zinc oxide.


1959 ◽  
Vol 32 (3) ◽  
pp. 739-747 ◽  
Author(s):  
J. R. Dunn ◽  
J. Scanlan

Abstract The thermal and photochemical aging of extracted dicumyl peroxide-, TMTD (sulfurless)- and santocure-vulcanized rubber, in presence of a number of metal and alkylammonium dithiocarbamates, has been investigated by measurements of stress relaxation. The dithiocarbamates have a considerable protective action upon the degradation of peroxide- and TMTD-vulcanizates, but they accelerate stress decay in santocure-accelerated vulcanizates. The reasons for this behavior are discussed. It is suggested that the excellent aging properties of unextracted TMTD vulcanizates are due to the presence of zinc dimethyldithiocarbamate formed during vulcanization.


2009 ◽  
Vol 23 (13-14) ◽  
pp. 1763-1786 ◽  
Author(s):  
Ganesh C. Basak ◽  
Abhijit Bandyopadhyay ◽  
Y. K. Bharadwaj ◽  
S. Sabharwal ◽  
Anil K. Bhowmick

1936 ◽  
Vol 9 (1) ◽  
pp. 70-73
Author(s):  
Yoshio Tanaka ◽  
Shû Kambara ◽  
Jirô Noto

Abstract To study the effect of solvents on the elastic properties of vulcanized rubber, the following three points were investigated. 1. The swelling maximum obtained by various mixed solvents. 2. The stress-strain curves of rubber swollen to different degrees. 3. Time-swelling and time-deswelling curves. The spiral theory of molecular structure of rubber proposed by Fikentscher and Mark is utilized to explain the experimental results.


2021 ◽  
pp. 1-13
Author(s):  
Fuzuli A Nasirov ◽  

Sustainable development, the design of green and economically feasible processes to produce synthetic polymers is one of the major needs and biggest challenges. Catalysis of polymerization processes is among the most important applications within the field of nanoscience. Intensive research is being conducted and considerable success has been achieved in the heterogenization of various homogeneous catalysts on nano supports for polymerization of olefins and dienes. The large surface area of various nanomaterials qualifies them quite naturally to act either as a heterogeneous promoter for catalytic reactions or as a support for the heterogenization of homogeneous catalysts. To the polymerization of olefins and dienes by using nanocatalysts are devoted significant numbers of published papers, but to elucidate the possible effect of both the type and properties of nano supports and their sizes and amounts on the activity and stereoselectivity of heterogenized catalysts and the properties of the obtained polymers are needed more detailed studies. This review attempted to collect some published research materials in the field of the nanocatalysis of olefins and dienes polymerization processes and our main aim is to assess the critical points and to indicate the future perspectives and possible strategies in this area of research. We are confident that this review will be a helpful companion and deliver key hints to those, in academia and in the industry, who decide to move their research interest in this direction


2005 ◽  
Vol 21 (3) ◽  
pp. 183-199
Author(s):  
G.K. Jana ◽  
C.K. Das

De-vulcanization of vulcanized elastomers represents a great challenge because of their three-dimensional network structure. Sulfur-cured gum natural rubbers containing three different sulfur/accelerator ratios were de-vulcanized by thio-acids. The process was carried out at 90 °C for 10 minutes in an open two-roll cracker-cum-mixing mill. Two concentrations of de-vulcanizing agent were tried in order to study the cleavage of the sulfidic bonds. The mechanical properties of the re-vulcanized rubber (like tensile strength, modulus, tear strength and elongation at break) were improved with increasing concentrations of de-vulcanizing agent, because the crosslink density increased. A decrease in scorch time and in optimum cure time and an increase in the state of cure were observed when vulcanized rubber was treated with high amounts of de-vulcanizing agent. The temperature of onset of degradation was also increased with increasing concentration of thio-acid. DMA analysis revealed that the storage modulus increased on re-vulcanization. From IR spectroscopy it was observed that oxidation of the main polymeric chains did not occur at the time of high temperature milling. Over 80% retention of the original mechanical properties (like tensile strength, modulus, tear strength and elongation at break) of the vulcanized natural rubber was achieved by this mechanochemical process.


2020 ◽  
Vol 81 ◽  
pp. 106173 ◽  
Author(s):  
Suppachai Sattayanurak ◽  
Kannika Sahakaro ◽  
Wisut Kaewsakul ◽  
Wilma K. Dierkes ◽  
Louis A.E.M. Reuvekamp ◽  
...  

2020 ◽  
Vol 990 ◽  
pp. 262-266
Author(s):  
Prathumrat Nu-Yang ◽  
Atiwat Wiriya-Amornchai ◽  
Jaehoon Yoon ◽  
Chainat Saechau ◽  
Poom Rattanamusik

Thermoplastic vulcanizates or TPVs is a type of materials exhibiting excellent properties between thermoplastic and elastomer by combining the characteristics of vulcanized rubber with the processing properties of thermoplastics. This research aims to study the effect of thermal aging on the morphology and mechanical properties of thermoplastic vulcanizates (TPVs) based on a mixture of natural rubber (NR) and polystyrene (PS). TPVs samples were prepared using the internal mixer at a mass ratio of NR/PS 70/30, 50/50, 30/70 and 0/100. Tensile properties and impact strength showed that when the amount of NR increased tends of impact strength and elongation at break increased but tends of tensile strength decreased. On the other hand, tends of tensile strength for thermal aging at 70°C for 3 days increased when the amount of PS increase. The blending ratio of NR / PS at 70/30 is the best. It gave a worthy increase from 19.94 MPa to be 25.56 MPa (28.18%).


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