Influence of Exposing Vulcanized Rubber to Light on Its Subsequent Aging in the Dark

1944 ◽  
Vol 17 (1) ◽  
pp. 216-220
Author(s):  
J. R. Scott
Keyword(s):  
Tensile Strength ◽  
Accelerated Aging ◽  
Subsequent Aging ◽  
Oxygen Bomb ◽  
Vulcanized Rubber ◽  
Effect Of Light

Abstract The present experiments confirm the observations of Morgan and Naunton by showing that exposure of vulcanized rubber to light may affect the results of oxygen-bomb aging tests made some days, or perhaps even weeks, afterwards. They show also that a few days' exposure to even diffused daylight may noticeably lower the tensile strength of unaged rubber. With normal, i.e., not transparent, rubbers the effect of light on subsequent aging is small, and indeed does not seem to be noticeable at all in relatively slow aging tests, such as that in the Geer oven. Nevertheless, it is clearly advisable, as a precaution, to avoid unnecessary exposure to light of rubbers that are to be subjected to accelerated aging tests.

Aging of Rubber in the Oxygen Bomb at Room Temperature

1943 ◽  
Vol 16 (4) ◽  
pp. 924-925
Author(s):  
J. R. Scott
Keyword(s):  
Tensile Strength ◽  
Oxygen Concentration ◽  
Room Temperature ◽  
Accelerated Aging ◽  
Natural Aging ◽  
Tensile Tests ◽  
Oxygen Bomb ◽  
Vulcanized Rubber ◽  
Accelerated Aging Test ◽  
Aging Test

Abstract The work described below was carried out as a first step in determining whether an oxygen-bomb test at room temperature could be used as an accelerated aging test for unvulcanized rubber compositions, e.g., as used on surgical and adhesive plasters and for combining shoe fabrics, because a high-temperature test is unsatisfactory in such cases, owing to the melting of the compositions. The only infallible way of assessing the value of an accelerated test for such compositions is by comparison with natural aging, but as this is a very lengthy process and as the deterioration is difficult to measure quantitatively, it was decided to make preliminary tests on the effect of high oxygen concentration at room temperature by using vulcanized rubber. Although the results proved to be negative so far as the original purpose of the work was concerned, it is considered of interest to place them on record in view of the prominence given in some papers on aging to the relationship between oxygen concentration and rate of oxidation and deterioration of rubber. A mix composed of rubber 100, sulfur 3, zinc oxide 5, stearic acid 1, and diphenylguanidine 0.75, was vulcanized for 30 minutes at 153° C. Tensile tests, using standard ring-specimens and the Schopper machine, were made on unaged specimens and on specimens that had been aged (1) in an oxygen bomb at 300 lb. per sq. in. oxygen pressure and at room temperature (about 10° C), (2) in a Geer oven at 70° C. Four rings were used for each test, the tensile strength and breaking elongation figures quoted being the average for the two rings giving the highest tensile strength, and the figures for the elongations at constant loads the average of all four rings.

The Direct Determination of Oxygen in Rubber. The Adaptation of the Ter Meulen Method to Rubber and Its Application to the Study of Aging

1939 ◽  
Vol 12 (2) ◽  
pp. 269-282 ◽  
Author(s):  
H. I. Cramer ◽  
I. J. Sjothun ◽  
L. E. Oneacre
Keyword(s):  
Tensile Strength ◽  
Physical Properties ◽  
Direct Determination ◽  
Sulfur Poisoning ◽  
Oxidation Products ◽  
Oxygen Bomb ◽  
Vulcanized Rubber ◽  
Relationship Of ◽  
The Relationship

Abstract The ter Meulen method for the direct determination of oxygen has been adapted, with modifications, to the analysis of raw and vulcanized rubbers. Raney nickel has been found to be quite effective as the reducing catalyst and to be satisfactorily resistant to sulfur poisoning. The method has been applied to the study of the aging of vulcanized rubber in the Geer oven and oxygen bomb. From this study the following conclusions may be drawn: (1) The increase in combined oxygen is greater in the oxygen bomb than in the Geer oven. (2) Deterioration of rubber in the oxygen bomb involves oxidation primarily, whereas that occurring in the Geer oven involves not only oxidation but also thermal decomposition followed by volatilization of oxidation products. (3) The effectiveness of an antioxidant in retarding the absorption of oxygen in oxygen-bomb aging agrees well with its ability to maintain the physical properties of the stock in which it is present. (4) The deterioration in physical properties of a rubber stock in the oxygen bomb during the early stages of aging is a linear function of the increase in combined oxygen. For stocks containing antioxidants and diphenylguanidine as the accelerator, an increase in combined oxygen of approximately 1.2% corresponds to a decrease in tensile strength of 50%. (5) The relationship of increase in combined oxygen to decrease in tensile strength seems to be affected not only by antioxidants, but also by accelerators of vulcanization.

A Manometric Test for Oxygen Absorption by Vulcanized Rubber

1942 ◽  
Vol 15 (1) ◽  
pp. 83-90
Author(s):  
Robert H. Johnson
Keyword(s):  
Tensile Strength ◽  
Oxygen Absorption ◽  
Aging Behavior ◽  
Strength Deterioration ◽  
Oxygen Bomb ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Manometric Method ◽  
Set Up ◽  
Bomb Method

Abstract An apparatus can be set up in laboratory glassware that will confirm the results obtained by Dufraisse in his manometric test for oxygen absorption. It has been shown that different rubber compounds possess different tendencies to absorb oxygen. It has also been shown that the differences in the rate at which rubber compounds absorb oxygen are comparable with those differences found in the rate of tensile-strength deterioration of the same compounds aged in the oxygen bomb. This modified Dufraisse manometric method is convenient, efficient, accurate and, above all, a speedy method for measuring the relative aging behavior of vulcanized rubber compounds. Within two hours it is possible to have the results by this method, whereas it is necessary to wait from four days to two weeks for such information by the oxygen bomb method.

scholarly journals Evaluation of the Impact of Organic Fillers on Selected Properties of Organosilicon Polymer

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1103
Author(s):  
Sara Sarraj ◽  
Małgorzata Szymiczek ◽  
Tomasz Machoczek ◽  
Maciej Mrówka
Keyword(s):  
Tensile Strength ◽  
Natural Fiber ◽  
Accelerated Aging ◽  
Strength Properties ◽  
Visual Observation ◽  
Walnut Shell ◽  
Pistachio Shell ◽  
Thermoplastic Matrix ◽  
Static Tensile ◽  
The Impact

Eco-friendly composites are proposed to substitute commonly available polymers. Currently, wood–plastic composites and natural fiber-reinforced composites are gaining growing recognition in the industry, being mostly on the thermoplastic matrix. However, little data are available about the possibility of producing biocomposites on a silicone matrix. This study focused on assessing selected organic fillers’ impact (ground coffee waste (GCW), walnut shell (WS), brewers’ spent grains (BSG), pistachio shell (PS), and chestnut (CH)) on the physicochemical and mechanical properties of silicone-based materials. Density, hardness, rebound resilience, and static tensile strength of the obtained composites were tested, as well as the effect of accelerated aging under artificial seawater conditions. The results revealed changes in the material’s properties (minimal density changes, hardness variation, overall decreasing resilience, and decreased tensile strength properties). The aging test revealed certain bioactivities of the obtained composites. The degree of material degradation was assessed on the basis of the strength characteristics and visual observation. The investigation carried out indicated the impact of the filler’s type, chemical composition, and grain size on the obtained materials’ properties and shed light on the possibility of acquiring ecological silicone-based materials.

Effects of Accelerated Aging Period of Time at 180°C on Tensile Property of Plain Woven Fabric/Epoxy Resin Laminated Composites

2012 ◽  
Vol 182-183 ◽  
pp. 76-79 ◽  
Author(s):  
Lei Lei Song ◽  
Quan Rong Liu ◽  
Jia Lu Li
Keyword(s):  
Tensile Strength ◽  
Carbon Fiber ◽  
Epoxy Resin ◽  
Laminated Composites ◽  
Accelerated Aging ◽  
Woven Fabric ◽  
Accelerated Ageing ◽  
Time Intervals ◽  
Composite Samples

In this paper, carbon fiber reinforced resin matrix composites were produced by stacking eight pieces of carbon fiber woven plain fabric and subjected to accelerated ageing. Accelerated ageing was carried out in oven at 180°C for three different time intervals (60 hours, 120 hours and 180 hours). The influence of different ageing time intervals at 180°C on tensile properties of laminated composites was examined, compared with the composites without aging. The appearance and damage forms of these laminated composites were investigated. The results revealed that the tensile strength of the laminates declined significantly after long term accelerated aging at 180°C. The average tensile strengths of composite samples aged 60 hours, 120 hours, and 180 hours period of time at 180°C are 80.36%, 79.82%, 76.57% of average tensile strength of composite samples without aging, respectively. The high temperature accelerated aging makes the resin macromolecular structure in the composites changed, and then the adhesive force between fiber bundles and resin declines rapidly which result in the tensile strength of composites aged decrease. This research provides a useful reference for long term durability of laminated/epoxy resin composites.

Mechanochemical Devulcanization of Vulcanized Gum Natural Rubber

2005 ◽  
Vol 21 (3) ◽  
pp. 183-199
Author(s):  
G.K. Jana ◽  
C.K. Das
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Natural Rubber ◽  
Three Dimensional ◽  
Elongation At Break ◽  
Tear Strength ◽  
Vulcanized Rubber ◽  
Dimensional Network ◽  
Polymeric Chains ◽  
Cure Time

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.

Devulcanization of Automobile Scrap Tyres by a Mechanochemical Process

2005 ◽  
Vol 21 (4) ◽  
pp. 319-331 ◽  
Author(s):  
G.K. Jana ◽  
C.K. Das
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Chemical Process ◽  
Crosslink Density ◽  
Diallyl Disulfide ◽  
Density Data ◽  
Vulcanized Rubber ◽  
Rubber Waste ◽  
Mechanical Shearing ◽  
Vulcanization Process

The de-vulcanization of rubber waste poses a challenging economical, environmental and social problem. We propose a new de-vulcanization process to re-use the rubber waste. It is a mechano-chemical process (MCP), where the waste is de-vulcanized by a combination of mechanical shearing, heat (110 °C) and the use of a de-vulcanizing agent (diallyl disulfide). A new look at the de-vulcanization mechanism and the influence of the de-vulcanizing agent on the mechanical properties of the ultimate re-vulcanized rubber is also presented. One of the most interesting observations is that the retention of tensile strength of the re-vulcanized rubber with respect to the original tyre was 34.9% when de-vulcanized in the absence of diallyl disulfide and 72.4% in its presence. The formation of extra crosslinks in those re-vulcanized rubbers containing disulfide was confirmed from crosslink density data and from TGA results. DMA analysis revealed that the storage modulus also increased for re-vulcanized rubber containing the disulfide.

The Effect of Thermal Aging on Mechanical Properties and Morphological Properties of Thermoplastic Vulcanizates Based on Natural Rubber and Polystyrene

2020 ◽  
Vol 990 ◽  
pp. 262-266
Author(s):  
Prathumrat Nu-Yang ◽  
Atiwat Wiriya-Amornchai ◽  
Jaehoon Yoon ◽  
Chainat Saechau ◽  
Poom Rattanamusik
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Impact Strength ◽  
Natural Rubber ◽  
Thermal Aging ◽  
Morphological Properties ◽  
Vulcanized Rubber ◽  
Thermoplastic Vulcanizates ◽  
Internal Mixer ◽  
Processing Properties

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%).

The Effect of Softeners in Rubber

1953 ◽  
Vol 26 (1) ◽  
pp. 152-155
Author(s):  
Ira Williams
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
High Modulus ◽  
Mineral Oils ◽  
Cohesive Forces ◽  
Commercial Use ◽  
Effect Of Solvents ◽  
Vulcanized Rubber ◽  
Unfavorable Effect ◽  
The Cost

Abstract The use of oils and liquid softeners to assist in the mastication and processing of rubber or to produce softer vulcanized stocks has been standard practice since the early commercial use of rubber. More recently certain synthetic rubbers, polymerized under special conditions, have been treated with rather large amounts of mineral oils, with a resulting decrease in the cost of the rubber and apparently with no unfavorable effect on the rubber in most instances. A number of investigators have reported the effect of swelling agents on the properties of vulcanized rubber. Busse discusses the effect of solvents in a general way. Tiltman and Porritt conclude that the decrease in modulus caused by swelling in benzene is caused by a “loosening of cohesive forces.” Tire treads of natural rubber containing such softeners as pine tar and mineral rubber decrease in wear resistance in proportion to the softener content. Well vulcanized rubber of high modulus is most resistant to swelling in oils. Naunton, Jones, and Smith find that unaccelerated stocks lose the most tensile strength after being swollen, that milling of the raw rubber increases swelling, and that the presence of softeners in the rubber during vulcanization reduces the oil resistance. A limited amount of swelling has been reported to have little effect on the tensile strength of vulcanized natural rubber. Bourbon points out that separating the rubber molecules with solvent decreases the rate of vulcanization.

Aging and Fatigue of Aerosol Jet-Printed Nano-Ag Traces on Flexible Substrate

2020 ◽  
Vol 143 (2) ◽  
Author(s):  
Arun Raj ◽  
Rajesh Sharma Sivasubramony ◽  
Manu Yadav ◽  
Sanoop Thekkut ◽  
Gurvinder Singh Khinda ◽  
...  
Keyword(s):  
Fatigue Resistance ◽  
Selection Process ◽  
Flexible Substrate ◽  
Accelerated Aging ◽  
Organic Matrix ◽  
Subsequent Aging ◽  
Long Term Storage ◽  
Order Of Magnitude ◽  
Sintering Conditions ◽  
The Stability

Abstract Conducting traces on a flexible substrate often have to survive significant and repeated deformation, making their fatigue resistance and the stability of it during long-term storage and use a potential concern. The question of stability is obvious in the case of, for example, screen or ink jet-printed traces where the organic matrix remains a critical part of the structure. We show it also to be important for nano-Ag traces that are sintered to ensure metallic bonding between the particles while eliminating most of the organics. We also show conventional accelerated aging tests to be potentially confusing or misleading for such traces, depending among other on practical limitations on sintering conditions. Examples are presented of how the fatigue resistance of application relevant aerosol jet-printed nano-Ag traces may degrade relatively rapidly at moderate temperatures. Even after “optimized” sintering at a much higher temperature subsequent aging at 75 °C for only 100 h led to an order of magnitude reduction in the fatigue life in subsequent mild cycling. The rate of degradation is certain to vary with the design and the ink used as well as with sintering conditions, making it important to account for it all in materials selection, process optimization, and assessments of practical life.

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