Filler Reinforcement of Liquid Elastomers

1973 ◽  
Vol 46 (1) ◽  
pp. 161-177 ◽  
Author(s):  
D. Rivin ◽  
R. G. True

Abstract To realize the potential processing benefits of liquid rubbers, methods must be developed for producing acceptable reinforced compounds which retain the inherent rheological advantages of the uncured polymer. The most promising commercially available liquid rubbers are functionally terminated low molecular weight analogs of common general-purpose elastomers such as poly-(butadiene) or butadiene copolymers. In principle, these low molecular weight polymers can be vulcanized by a combination of chain extension and cross-linking to yield vulcanizates comparable to those from solid elastomers. Both cure reactions can be carried out simultaneously with a chemically specific polyfunctional coupling agent, or alternatively, chain extension with a difunctional reactant can be followed by use of accelerated sulfur or equivalent crosslinking agents. In contrast to certain polar polymers, liquid hydrocarbon rubbers yield relatively weak vulcanizates which are unsuitable for mechanical and tire applications. Physical properties are greatly improved by addition of up to 60 phr of reinforcing fillers such as carbon black or precipitated silica, but at the expense of flow behavior. Important filler-dependent properties of representative liquid rubbers will be described, with emphasis on the rheology of reinforced compounds.

2006 ◽  
Vol 11-12 ◽  
pp. 387-390 ◽  
Author(s):  
Si Yang Luo ◽  
Yu Zhang ◽  
Jing Bo Zhao

Low molecular weight poly(butylene adipate) (PBA) was synthesized by melt polycondensation. The chain extension of the prepolymers was carried out using 2,2’-(1,4-phenylene)-bis(2-oxazoline) (PBOX) as chain-extender. The influencing factors including reaction temperature, oxazoline/-COOH molar ratio, and the molecular weight of prepolymers were studied. At the optimal chain-extending condition, PBA with Mn of 38583 and Mw of 125497 was prepared. The structure of the chain-extended PBA was also characterized by the FTIR and 1H NMR.


1970 ◽  
Vol 43 (5) ◽  
pp. 1109-1115 ◽  
Author(s):  
E. A. Collins ◽  
T. Mass ◽  
W. H. Bauer

Abstract The flow behavior of low molecular weight liquid polybutadiene polymers was studied as a function of shear rate, temperature, and molecular structure. Measurements were made in the temperature range 15 to 50° C and shear rate range 1 to 15,000 sec−1 with a cone and plate and a capillary viscometer. Limiting low shear viscosity, flow activation energy, and critical shear rate marking onset of shear rate thinning were found to be strongly dependent upon the presence of functional groups such as hydroxyl, carboxyl, and nitrile. The modifying groups showed a greater effect than the molecular weight upon the properties measured.


1991 ◽  
Vol 227 ◽  
Author(s):  
Willi Volksen ◽  
D. Y. Yoon ◽  
J. L. Hedrick ◽  
D. Hofer

ABSTRACTThe modification of the pendant acid groups along the poly(amic acid) backbone in the form of alkyl ester groups leads to greatly improved polyimide precursors. These poly(amic alkyl esters) are characterized by the absence of hydrolytic instability due to elimimation of the “monomer-polymer” equilibrium associated with poly(amic acids), a broad imidization temperature regime, improved solubility characteristics, and enhanced mechanical properties. In the absence of hydrolytic instability, it is now possible to use an aqueous work-up of the polyimide precursor. This presents an attractive synthetic pathway for the preparation of well-defined, amine-terminated oligomers. Such oligomers can then be utilized both in the preparation of low molecular weight, chain-extendable polyimide precursors as well as polyimide block copolymers. The higher imidization temperatures offered by the “amic ester” chemistry allows for more efficient chain extension prior to imidization. Alternatively, the lack of the “monomer-polymer” equilibrium and accompanying propensity for monomer randomization reactions presents a potential pathway for the preparation of polyimide blends.


2014 ◽  
Vol 5 (8) ◽  
pp. 2709-2714 ◽  
Author(s):  
Zhongwei Ji ◽  
Jianghua Liu ◽  
Guosong Chen ◽  
Ming Jiang

In this paper, targeting a high-molecular-weight supramolecular polymer, chain extension of low-molecular-weight polymers (LMWPs) is achieved via the HSCT (Host-Stabilized Charge Transfer) of CB[8] (cucurbit[8]uril).


Author(s):  
G.K.W. Balkau ◽  
E. Bez ◽  
J.L. Farrant

The earliest account of the contamination of electron microscope specimens by the deposition of carbonaceous material during electron irradiation was published in 1947 by Watson who was then working in Canada. It was soon established that this carbonaceous material is formed from organic vapours, and it is now recognized that the principal source is the oil-sealed rotary pumps which provide the backing vacuum. It has been shown that the organic vapours consist of low molecular weight fragments of oil molecules which have been degraded at hot spots produced by friction between the vanes and the surfaces on which they slide. As satisfactory oil-free pumps are unavailable, it is standard electron microscope practice to reduce the partial pressure of organic vapours in the microscope in the vicinity of the specimen by using liquid-nitrogen cooled anti-contamination devices. Traps of this type are sufficient to reduce the contamination rate to about 0.1 Å per min, which is tolerable for many investigations.


1998 ◽  
Vol 1 (5) ◽  
pp. 166-174 ◽  
Author(s):  
Evelyn R Hermes De Santis ◽  
Betsy S Laumeister ◽  
Vidhu Bansal ◽  
Vandana Kataria ◽  
Preeti Loomba ◽  
...  

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