The Plasticization of Butadiene-Styrene Rubber

1956 ◽  
Vol 29 (2) ◽  
pp. 485-491 ◽  
Author(s):  
B. Karmin ◽  
B. Bets

Abstract 1. The kinetics of the plasticization of a butadiene-styrene copolymer on a cold laboratory mill was studied. It was established that, at temperatures of 20–30° C, the plasticity rises steadily and that, consequently, under these conditions a monodirectional destructive process takes place. 2. The kinetics of plasticization of a butadiene-styrene copolymer was investigated in a laboratory banbury at 140° C, both with and without a plasticization aid (chemical). Plasticization at a high temperature is accompanied by the simultaneous operation of the two reactions of destruction and structure formation proceeding at cross-purposes, and may be described by a kinetic equation of the type: P=P0 (1+a⋅m)(1−b⋅n) 3. Plasticized rubbers obtained by breakdown on a cold mill have a smaller capacity for recovery than those obtained by treatment in a boiler or a banbury at temperatures above 120° C. 4. Plasticized rubbers obtained by milling on a cold mill give stocks with higher tensile strength and higher relative elongation than rubbers plasticized by hot treatment. 5. The high recovery capacity of rubbers plasticized at elevated temperatures and the lowering of the physical and mechanical properties of vulcanizates of those rubbers are explained by the branched molecules which they form during structure formation.

1954 ◽  
Vol 27 (3) ◽  
pp. 615-621 ◽  
Author(s):  
B. Dogadkin ◽  
B. Karmin ◽  
I. Golberg

Abstract 1. It is shown that the tensile strength of vulcanized butadiene-styrene rubber is a linear function of the plasticity of the original material. 2. Proceeding from concepts of the presence during vulcanization of a number of opposing processes of structure formation and destruction, both of which influence the molecular weight of the rubber, a general equation is derived which expresses the kinetics of the change of tensile strength of a vulcanizate. 3. Experimental material is offered which proves the applicability of the proposed equation to the representation of the kinetics of vulcanization of mixtures of natural rubber containing relatively small sulfur contents, i.e., up to 3 per cent.


1951 ◽  
Vol 24 (2) ◽  
pp. 381-383 ◽  
Author(s):  
J. R. Scott

Abstract In unloaded ebonites made from butadiene-styrene copolymers, the resistance to plastic deformation at elevated temperatures is better the higher the styrene content of the copolymer, at least up to 46 per cent. An isoprene-styrene copolymer ebonite has poorer plastic-yield resistance than a corresponding butadiene-styrene ebonite. All the styrene-containing copolymers, however give ebonites more heat-resistant than natural rubber ebonite, the best giving yield temperatures 30° C above the latter. To attain the best plastic-yield resistance in butadiene-styrene ebonites, the amount of sulfur added should correspond to more than 1 atom (e.g., 1.2 or even 1.4 atoms) per butadiene molecule.


Alloy Digest ◽  
1983 ◽  
Vol 32 (3) ◽  

Abstract BRUSH Alloy 3 offers the highest electrical and thermal conductivity of any beryllium-copper alloy. It possesses an excellent combination of moderate strength, good corrosion resistance and good resistance to moderately elevated temperatures. Because of its unique physical and mechanical properties, Brush Alloy 3 finds widespread use in welding applications (RWMA Class 3), current-carrying springs, switch and instrument parts and similar components. This datasheet provides information on composition, physical properties, hardness, elasticity, and tensile properties as well as fatigue. It also includes information on corrosion resistance as well as casting, forming, heat treating, machining, joining, and surface treatment. Filing Code: Cu-454. Producer or source: Brush Wellman Inc..


2021 ◽  
pp. 009524432110203
Author(s):  
Sudhir Bafna

It is often necessary to assess the effect of aging at room temperature over years/decades for hardware containing elastomeric components such as oring seals or shock isolators. In order to determine this effect, accelerated oven aging at elevated temperatures is pursued. When doing so, it is vital that the degradation mechanism still be representative of that prevalent at room temperature. This places an upper limit on the elevated oven temperature, which in turn, increases the dwell time in the oven. As a result, the oven dwell time can run into months, if not years, something that is not realistically feasible due to resource/schedule constraints in industry. Measuring activation energy (Ea) of elastomer aging by test methods such as tensile strength or elongation, compression set, modulus, oxygen consumption, etc. is expensive and time consuming. Use of kinetics of weight loss by ThermoGravimetric Analysis (TGA) using the Ozawa/Flynn/Wall method per ASTM E1641 is an attractive option (especially due to the availability of commercial instrumentation with software to make the required measurements and calculations) and is widely used. There is no fundamental scientific reason why the kinetics of weight loss at elevated temperatures should correlate to the kinetics of loss of mechanical properties over years/decades at room temperature. Ea obtained by high temperature weight loss is almost always significantly higher than that obtained by measurements of mechanical properties or oxygen consumption over extended periods at much lower temperatures. In this paper, data on five different elastomer types (butyl, nitrile, EPDM, polychloroprene and fluorocarbon) are presented to prove that point. Thus, use of Ea determined by weight loss by TGA tends to give unrealistically high values, which in turn, will lead to incorrectly high predictions of storage life at room temperature.


2021 ◽  
Vol 11 (9) ◽  
pp. 3778
Author(s):  
Gene Yang ◽  
So-Yeun Kim ◽  
Changhee Sohn ◽  
Jong K. Keum ◽  
Dongkyu Lee

Considerable attention has been directed to understanding the influence of heterointerfaces between Ruddlesden–Popper (RP) phases and ABO3 perovskites on the kinetics of oxygen electrocatalysis at elevated temperatures. Here, we report the effect of heterointerfaces on the oxygen surface exchange kinetics by employing heteroepitaxial oxide thin films formed by decorating LaNiO3 (LNO) on La1.85Sr0.15CuO4 (LSCO) thin films. Regardless of LNO decoration, tensile in-plane strain on LSCO films does not change. The oxygen surface exchange coefficients (kchem) of LSCO films extracted from electrical conductivity relaxation curves significantly increase with partial decorations of LNO, whereas full LNO coverage leads to the reduction in the kchem of LSCO films. The activation energy for oxygen exchange in LSCO films significantly decreases with partial LNO decorations in contrast with the full coverage of LNO. Optical spectroscopy reveals the increased oxygen vacancies in the partially covered LSCO films relative to the undecorated LSCO film. We attribute the enhanced oxygen surface exchange kinetics of LSCO to the increased oxygen vacancies by creating the heterointerface between LSCO and LNO.


Sign in / Sign up

Export Citation Format

Share Document