Accelerated aging studies of UHMWPE. II. Virgin UHMWPE is not immune to oxidative degradation

2002 ◽  
Vol 61 (2) ◽  
pp. 323-329 ◽  
Author(s):  
A. A. Edidin ◽  
M. L. Villarraga ◽  
M. P. Herr ◽  
J. Muth ◽  
S. S. Yau ◽  
...  
Keyword(s):  
Oxidative Degradation ◽  
Accelerated Aging ◽  
Aging Studies

Aging Studies of Pu-238 and -239 Containing Calcium Phosphate Ceramic Waste-forms

2013 ◽  
Vol 1518 ◽  
pp. 73-78 ◽  
Author(s):  
Shirley K. Fong ◽  
Brian L. Metcalfe ◽  
Randall D. Scheele ◽  
Denis M. Strachan
Keyword(s):  
Calcium Phosphate ◽  
Accelerated Aging ◽  
Waste Form ◽  
Calcium Phosphate Ceramic ◽  
Ceramic Waste ◽  
Waste Forms ◽  
Aging Studies ◽  
Flow Through ◽  
Pyrochemical Reprocessing

ABSTRACTA calcium phosphate ceramic waste-form has been developed at AWE for the immobilisation of chloride containing wastes arising from the pyrochemical reprocessing of plutonium. In order to determine the long term durability of the waste-form, aging trials have been carried out at PNNL. Ceramics were prepared using Pu-239 and -238, these were characterised by PXRD at regular intervals and Single Pass Flow Through (SPFT) tests after approximately 5 yrs.While XRD indicated some loss of crystallinity in the Pu-238 samples after exposure to 2.8 x 1018 α decays, SPFT tests indicated that accelerated aging had not had a detrimental effect on the durability of Pu-238 samples compared to Pu-239 waste-forms.

Accelerated Heat-Aging Studies on Fluorosilicone Rubber

1975 ◽  
Vol 48 (5) ◽  
pp. 944-952 ◽  
Author(s):  
S. H. Kalfayan ◽  
R. H. Silver ◽  
A. A. Mazzeo
Keyword(s):  
Weight Loss ◽  
Stress Relaxation ◽  
Repeat Unit ◽  
Accelerated Aging ◽  
Basic Mechanism ◽  
Inert Atmosphere ◽  
Polymer Backbone ◽  
Aging Studies ◽  
Relaxation Measurements ◽  
Fluorosilicone Rubber

Abstract The accelerated aging of a vulcanizate of fluorosilicone rubber was studied by four methods: infrared spectroscopy, GPC, weight loss, and stress relaxation, with the object of gathering information pertinent to understanding the basic mechanism of its aging. No changes were observed in infrared spectra of the rubber aged in air up to 315°C although severe degradation took place, as evidenced by high weight loss and drastic change in the physical condition of the test samples. It was concluded that although the polymer degrades, there is no change detectable within the precision of the analytical methods in the structure of the repeat unit of the elastomer. The gel-permeation chromatogram of unheated rubber showed peaks at MW 450 000 (95%) and 630 (5%). The low-molecular-weight component is very likely the cyclic tetramer of λ,λ′,λ″-trifluoropropylmethylsiloxane, the principal monomer of the FVMQ used. Heat aging increased the concentration of the 630 MW component, but rate studies were prevented by complications resulting from solvent-induced rubber degradation. Rapid decrease in the MW of FVMQ, as found by GPC, indicated random scission in the polymer backbone, as opposed to ordered unzipping of the repeat unit. The same conclusion was reached from the effects of crosslink density on stress relaxation. Activation energies obtained from weight-loss measurements (104 kJ/mol) were lower than those obtained from stress-relaxation measurements, (150–155 kJ/mol), suggesting that the processes being measured in each case may not be the same. Chemical stress relaxation takes place more rapidly in the presence of air than in an inert atmosphere, and intermittent stress-relaxation measurements indicate that crosslinks form during thermal aging in air, their rate first increasing and then decreasing.

Rubber Oxidation and Aging Studies Safe Limits of Sample Thickness

1951 ◽  
Vol 24 (4) ◽  
pp. 999-1016
Author(s):  
George W. Blum ◽  
J. Reid Shelton ◽  
Hugh Winn
Keyword(s):  
Natural Rubber ◽  
Accelerated Aging ◽  
Sample Thickness ◽  
Oxygen Absorption ◽  
Absorption Data ◽  
Synthetic Rubber ◽  
Constant Rate ◽  
Aging Studies ◽  
Safe Limits ◽  
Natural Rubber Vulcanizates

Abstract Safe limits of sample thickness for rubber oxidation and aging studies, such that the chemical reaction rather than the rate of diffusion will be rate-controlling have been investigated for natural-rubber vulcanizates and for four synthetic-rubber types. For studies involving the entire range of oxidation, including the autocatalytic stage of rapid oxygen absorption, the conventional 0.075-inch thickness is frequently not satisfactory for accelerated aging and oxidation studies if it is desired to avoid limitation by diffusion. Only in the GR-S black stock was this thickness found to be satisfactory up to a temperature of 100° C. The other stocks, including natural rubber, Butaprene-NXM, and Neoprene black and gum stocks all require thinner samples to ensure that the observed rate of oxygen absorption is free of limitation by diffusion. A method of calculating the probable limiting value of sample thickness, above which the rate of oxidation in the autocatalytic stage is limited by diffusion, has been developed on the basis of volumetric oxygen absorption data obtained with GR-S. The method has also been applied to natural-rubber vulcanizates and to other synthetic-rubber types to locate the approximate limiting values at various temperatures for oxidation and aging studies which extend into the autocatalytic stage of rapid reaction. The constant-rate period of oxidation is more important from a practical point of view than the autocatalytic stage, since properties are so seriously degraded as to make the rubber of little value before it reaches the final stage of rapid oxidation. Somewhat thicker samples may be used for studies that are confined to the earlier stages of oxidation. A 0.075-inch sample is free of limitation by diffusion in the constant-rate stage in the following cases: GR-S black and gum stocks at 110° C; Hevea black with added antioxidant at 100° C; and uninhibited Hevea black and gum stocks at 60° C. A 0.040-inch sample is satisfactory in this range for: uninhibited Hevea black at 100° and gum at 80° C; Butaprene-NXM black at 100° and gum at 90° C; and Neoprene black and gum stocks at 100° C.

The Oxidative Aging of a Compounded Natural Rubber Vulcanizate

1978 ◽  
Vol 51 (1) ◽  
pp. 1-6 ◽  
Author(s):  
R. A. Pett ◽  
R. J. Tabar
Keyword(s):  
Natural Rubber ◽  
Reaction Rate ◽  
Oxidative Degradation ◽  
Accelerated Aging ◽  
Zero Order ◽  
Elongation At Break ◽  
Oxidative Aging ◽  
Zero Order Reaction ◽  
The Impact

Abstract For the type of natural rubber compound used in the impact absorbing bumper system, it has been shown that an apparent zero order reaction rate is valid for the degradation of tensile strength, elongation at break and tear strength during oven aging. The zero order rate applies to aging times beyond an induction period and prior to the onset of hardening. Since the rates follow the Arrhenius equation for rate-temperature dependence, accelerated aging can be readily applied to the prediction of long term changes in properties (within the temperature range of 82–171°C). The magnitude of the activation energy determined from losses in mechanical properties indicates the dominance of oxidative degradation as the mechanism of the losses in properties.

Accelerated Aging Studies for Organic Optical Data Storage Media

1989 ◽  
Author(s):  
David E. Nikles ◽  
Charles E. Forbes ◽  
Harris A. Goldberg ◽  
Robert E. Johnson ◽  
Rachel S. Kohn ◽  
...  
Keyword(s):  
Data Storage ◽  
Accelerated Aging ◽  
Optical Data Storage ◽  
Optical Data ◽  
Storage Media ◽  
Aging Studies

A lyophilized hemoglobin control prepared from stroma-free hemolysates.

1980 ◽  
Vol 26 (2) ◽  
pp. 305-308 ◽  
Author(s):  
D P Bonderman ◽  
G J Proksch ◽  
S Haskins
Keyword(s):  
Accelerated Aging ◽  
Human Erythrocytes ◽  
Polyhydroxy Compounds ◽  
Aging Studies ◽  
One Year

Abstract We prepared a stable lyophilized hemoglobin control from human erythrocytes by removing stroma with calcium and Ficoll. Addition of polyhydroxy compounds enhanced reconstitution and stability. The lyophilized product was stable during one year of use in a service laboratory. Accelerated aging studies demonstrated the potential of up to two years of stability, with methemoglobin increasing at a projected rate of approximately 6% per year. Reconstituted, the control gave reproducible values for at least five days when refrigerated.

scholarly journals The Influence of the Accelerated Aging Conditions on the Properties of Polyolefin Geogrids Used for Landfill Slope Reinforcement

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1874
Author(s):  
Agnieszka Kiersnowska ◽  
Wojciech Fabianowski ◽  
Eugeniusz Koda
Keyword(s):  
Mechanical Properties ◽  
Relative Elongation ◽  
Oxidative Degradation ◽  
Accelerated Aging ◽  
Melt Flow Index ◽  
Flow Index ◽  
Scanning Calorimetry ◽  
Oxidation Induction Time ◽  
Aging Test ◽  
Different Temperatures

Polyolefin geosynthetics are susceptible to oxidative degradation, which in turn leads to diminished mechanical properties in geotechnical constructions. When using these materials, it is extremely important to determine their durability over time in particularly aggressive conditions. In order to prolong the life of a geosynthetic material, antioxidants are added during the manufacturing process. The function of antioxidants is to prevent polymer oxidation reaction in time. As the antioxidant content is depleted, the polymer becomes less protected towards oxidative attacks. This article describes the aging process of uniaxial (high density polyethylene) HDPE geogrids under the influence of chemical and environmental factors. Evaluations of accelerated aging test of the uniaxial HDPE geogrids were incubated in simulated landfill conditions for a period of 12 months. Three temperatures (25 °C, 45 °C, and 75 °C) were selected for carrying out the aging experiments in aqueous solutions mimicking landfill conditions. The changes observed by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and melt flow index (MFI) correlate with the mechanical properties of the aged geogrid. No significant changes in the FTIR and MFI were observed over the 12 months of accelerated aging tests at none of the three different temperatures. The oxidation induction time (OIT) test showed no antioxidant remaining in the geogrid following eight months of aging test at 75 °C. No significant changes in the influence of accelerated aging tests on the average relative elongation at 25 °C and 45 °C of the tested material were observed. Accelerated aging tests at 75 °C showed that the mean elongation of 12.12% for the sample not subjected to accelerated aging tests (new sample) increased to 19.32% (after 12 months of incubation).

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