Polymeric Schiff bases. XIII - The direct synthesis of cross-linked polymeric azomethines.
Cross-linked polymers obtained by direct reaction of aryl polycarbonyls with aryl polyamines, studying char yields effect
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Cross-linked polymers obtained by direct reaction of aryl polycarbonyls with aryl polyamines, studying char yields effect
Cross-links effect on char yields of azomethine polymers produced by aryl diamines with aryl diketones
Schiff base cross-links effect on synthesis of polymeric azomethines produced by bis exchange reactions, carbonyl and amine
Polymer structure and cross-link density effects on thermal analysis of phenol-formaldehyde polymers pyrolysis products
Cross linking of polyvinylidene fluoride by gamma radiation
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Cross link density and polymer structure effects on thermal analysis of phenol formaldehyde polymers
The mechanical properties of an elastomer, including rupture and its time dependence, are defined uniquely by a tensile property surface in normalized stress-strain-time coordinates. In practice, the property surface is determined from short-time constant strain-rate uniaxial tests. By using the time reduction properties of both temperature and cross-link density, an effective time scale of over ten decades of log time can be covered. Changes in cross-link density, filler content, or swelling do not affect the limits of the property surface when plotted in logarithmic coordinates but merely shift their positions. The shape, however, may be modified in certain cases. The service life of an elastomer in the absence of aging reactions can be estimated from the property surface and expected in-use conditions such as strains (static or dynamic).
Aromatic polyester, PEN-2,6, is improved through cross-linking effected by radiation. Polymer retains properties of high tensile strength and toughness and stability at high temperatures.
Torsional creep measurements on cross-linked natural rubber vulcanizates
Plastic scintillator produced by the substitution of epoxy resins for the commonly used polystyrene is easy to cast, stable at room temperature, and has the desirable properties of a thermoset or cross-linked system. Such scintillators can be immersed directly in strong solvents, an advantage in many chemical and biological experiments.
Silver-zinc cells having a separator system of cross-linked high-density polyethylene with a methacrylic acid graft withstand corrosion when subjected to thermal sterilization treatments.
Process yields difunctional isobutylene polymers ranging in molecular weight from 1150 to 3600. These polymers have the potential for copolymerization and cross-linking with other monomers to form elastomeric materials.
A prototype all carbon triode ultrahigh vacuum gage was fabricated and tested. The gage exhibited a sensitivity of 3.7 per torr for nitrogen and an X-ray background approximately 0.1 as large as would be expected of a metal gage of the same design. The gage made from these materials, showed good sensitivity and durability. A practical technique was developed for bonding carbon components together without metal fasteners. The bond is made with a cross-linked phenolic resin which is converted to vitreous carbon by a careful pyrolysis procedure. The resulting bonds are strong, electrically conductive, and can withstand repeated excursions to 2500 K in vacuum. Measurements of adsorption and outgassing characteristics of four refractory carbons have confirmed that such materials are suitable for use in ultrahigh vacuum and that some are superior refractory metals in man respects.
Molecular weight fractions of linear polyethylene were irradiated at 133 C, in the completely molten and highly crystalline states, for the purpose of assessing the importance of chain-scission processes and establishing the critical conditions for gelation. The partitioning between sol and gel in either state was found to adhere to the theory for the intermolecular cross-linking of monodisperse species for dosages just beyond the gel point. Deviations from theory occurred as the dosage was increased further. It was concluded that main-chain scission, at these temperatures, is not a significant process. High molecular weight samples in the completely molten state obeyed the Flory-Stockmayer condition for critical gelation.
The mechanical properties of elastomers, including rupture and its time dependence, can be semiquantitatively predicted from nine molecular parameters which are characteristic for a given species, from the initial molecular weight of a sample before cross-linking and from the effective chain concentration (which must still be determined for each vulcanizate). Only two empirical quantities are involved - the Plazek retardation function for entanglement slippage and a related constant which serves to locate this function on the time scale. The theory leads to a new method of estimating fatigue lifetimes from short-time data.
Tests were carried out on both synthetic and real wash water derived from clothes laundry to determine the utility of reverse osmosis in recovering the water for recycle use. A blend membrane made from cellulose di- and triacetates, and a cross-linked cellulose acetate/methacrylate were evaluated. Both were found acceptable. A number of detergents were evaluated, including a cationic detergent, sodium dodecyl sulfate, potassium palmitate, and sodium dodecylbenzenesulfonate. The tests were all made at a temperature of 165 F to minimize microbial growth. Long-term (15 to 30 day) runs were made at 600 and 400 psi on laundry water which was pretreated either by alum addition and sand filtration or by filtration only through 0.5 micron filters. A 30-day run was made using a 2-in. diameter by 22-in. long spiral module at 400 psig with filtering as the pretreatment. The membrane fouling by colloidal matter was found to be controllable. The unit produced initially 55 gal/day and 27 gal/day after 30 days.
A method for the synthesis and manufacturing of elastomeric compositions and articles containing quaternary nitrogen centers and condensation residues along the polymeric backbone of the centers is presented. Linear and cross-linked straight chain and block polymers having a wide damping temperature range were synthesized. Formulae for the viscoelastic cationic polymers are presented.